PRA-HEP97-7 Jet rates in deep inelastic scattering wherefrom comes the sensitivity to αs

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浩拉科技有限公司XP26微电子平衡用户说明书

浩拉科技有限公司XP26微电子平衡用户说明书

In the laboratory of Hella KGaA Hueck & Co., the daily routine of testing diverse samples used in the automotive industry is now greatly simplified and far more efficient with the employment of METTLER TOLEDO’s XP26 microbalance. Peter Broske, head of the mea-surement and test centre in the chemical analytics division of Hella KGaA Hueck & Co. is very enthusiastic about this new purchase.Diverse Tasks, One GoalHella KGaA Hueck & Co. runs its worldwide single chemical laboratory in Lippstadt, Ger-many. The site copes with an entire spectrum of the most diverse samples. The items which land on Peter Broske’s desk include complete headlight assemblies, complex electronicHella KGaA Hueck & CoTesting diverse samples used in the automotive industry Fogging tests (differential weighing application)XP26 Micro BalanceTurning Up the Lights for a Real Problem SolverAcademia Solutions Laboratory Case StudyAutomotive SolutionsMettler-Toledo AGLaboratory DivisionIm LangacherCH-8606 Greifensee, Switzerland Subject to technical changes.© Mettler-Toledo AG 07/09Printed in SwitzerlandGlobal MarCom Switzerlandcomponents, circuit boards, single microchips, granules, production containers and samples for air and water analysis for environmental protection and safety at work. Apart from in-process quality control, the lab also conducts analysis along-side the development of new prod-ucts. It is also the central point of contact for troubleshooting within production, processes and in the field. Efficient operations, high throughput, user-friendliness and flexible deployment of the relevant equipment are therefore essential. In addition, the automotive industry sets tight constraints in respect to accuracy, reproducibility and dead-line adherence, in order to greatly reduce the risk of handling errors. Peter Broske explains how well the XP26 microbalance from METTLER TOLEDO meets these requirements and shares some practical exam-ples with us.Difficult Sample Handling Solved by Smart SolutionsFogging tests are now standard Peter Broske, head of the measurement and test centre in the chemical analytics division of Hella KGaA Hueck & Co The microbalance in its surroundings at the analytical laboratory at Hella.practice in the automotive industry, which is still by far the primary customer segment for Hella. These tests involve studying the emission of water, organic solvents, addi-tives and plasticisers from compo-nents and assemblies. To perform the test the sample is heated andthe volatile components are con-densed onto a thin piece of cooled aluminum foil. These delicate foils are 50 - 80 mm in diameter and must not be bent or folded while determining tare weight, sample taking or back weighing. “The sensitivity and the size of the foil is the problem here”, explained Broske, just one crease or fold is enough to destroy the airtight seal between the sample and the sample holder. The luminous re-flectance of the folded edges would prevent any subsequent visual inspection of the condensates intended to determine their reflec-tance or impede any direct analysis under the FTIR microscope. This problem was solved thanks to the XP microbalance’s large weighing chamber and the hanging support of the weighing pan, situated at the rear of the weighing chamber”.The grid-type weighing pan can be easily removed and replaced with ErgoClips. The ErgoClip is a modi-fied weighing pan tailor-made to the individual needs of frequently used tare containers (e.g. volumet-ric flasks or Eppendorf tubes). Inthe case of fogging tests on alumi-num foil, Mr. Broske helped to find an optimum solution with his own modified version of the ErgoClipmicro basket. Mr. Broske also ben-efits from the balance’s application software: “The differential weighing application in the balance enables us to rule out any errors occurringduring manual notation of the tareweights. That’s a major plus!”Full Independency Thanks to METTLER TOLEDO Mr. Broske sums up the advan-tages of the XP microbalance:n Large weighing area and high degree of flexibility, thanks to SmartGrid and the ErgoClips n High accuracy for small samples and up to 52 grams with the possibility of directly weighing into various tare vessels n Differential weighing application accelerates work rate and lowers error riskn Short settling times and stable results within seconds thanksto the well-protected weighingchamber with external/internaldraft shields and unique hanging SmartGrid weighing pan n Automatic door opening facili-tates and accelerates operationprocedure He summarizes: “Given the con-stantly growing number and diver-sity of tasks and the required accu-racy and reproducibility, we would have had to outsource tests to oth-er laboratories. But these laborato-ries do not share our material and process know-how. Therefore, notzuviel Text。

Leviton ATLAS-X1 Cat 6A Component-Rated UTP QUICKP

Leviton ATLAS-X1 Cat 6A Component-Rated UTP QUICKP

Page 1 of 2APPLICATIONThe ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack supports 10GBASE-T networks. The jack is part of a complete ATLAS-X1 Cat 6A UTP system, ideal for the most demanding mission-critical network applications. The connector supports emerging technologies and will easily adapt to network trends.SPECIFICATIONThe jack shall meet or exceed the requirements for channel and component-level electrical transmission performance as described in ANSI/TIA-568.2-D (Cat 6A), ISO/IEC11801-1 (Class E A ), and EN 50173-1 (Class E A ). The jack shall be compliant with ANSI/TIA-1096-A, c(UL)us Listed, and be independently verified for electrical transmission performance and power delivery. The jack body shall be made of die-cast zinc and all plastic components shall be made of high-impact, fire-retardant plastic rated UL 94V-0. The jack shall support tool-free termination and re-termination and shall not require a specialized termination tool. The jack wiring shall be universal to accommodate T568A and T568B wiring schemes. The jack shall be available in 13 colors; more than established by the ANSI/TIA-606-C standard. The jack shall be offered in standard and shuttered styles and select jacks shall be supplied with interchangeable icons. The jack shall be compliant with IEEE 802.3 PoE Type 1, 2, 3, 4 (100 watts max).DESIGN CONSIDERATIONS• Use in any QUICKPORT™ housing to support Cat 6A UTP connectivity in surface-mount, flush-mount, or modular furniture outlets and field-configurable panels• Can be used in conjunction with other QUICKPORT snap-in modules for voice/data/video applications over UTP , coax, and fiber• To identify ports, use different colored modules andicons for each application (full selection of ANSI/TIA-606 compatible colors, 13 available)• Robust housing and shutter protects the jack in harsh environmentsATLAS-X1™ Cat 6A Component-Rated UTP QUICKPORT™ Jack6AUJK-xx6, ICONS-ICxFEATURES• Independently tested and guaranteed to exceed all component, permanent link, and channel margins• Patented Retention Force Technology™ (RFT) protects against tine damage and increases system longevity • For Power over Ethernet, RFT maintains contact force between plug and jack, preventing arcing from intermittent disconnects• Unique design supports tool-free termination andre-termination and requires no specialized termination tool • Short jack design supports a wider range of applications (e.g. shallow boxes, enclosures, bend radius, etc.)• Terminates from 26 to 22 AWG solid or stranded conductors for use on various cable types• Robust IDCs can withstand 20 re-termination cycles and jack contacts are tested for 750 plug-mating cycles to ensure system longevity• Available in 13 ANSI/TIA-606-C compatible colors • Tested and approved for use in air-handling spaces (plenum rating) in accordance with UL Standard 2043• Select jacks available with interchangeable icons (voice, data, A/V, blank) for easy ID• Jack with internal shutter protects against dust and debris • Solid metal body dissipates 53% more heat than plastic, minimizing damage from excess heat in PoE applications • Tine geometry prevents arcing damage where plug and jack make contactSTANDARDS & REGULATIONS• ANSI/TIA-568.2-D (Cat 6A)• ISO/IEC 11801-1 (Cat 6A)• EN 50173-1 (Cat 6A)• ANSI/TIA-1096-A (formerly FCC Part 68)• IEC 60603-7 (includes IEC 60512-5-2)• IEC 60512-99-002• IEEE 802.3 PoE Type 1, 2, 3, 4 (100 watts max)• Cisco UPOE, UPOE+ (90 watts max)• Power over HDBaseT™ PoH (95 watts max)• c(UL)us Listed (UL 1863)• UL 2043 Plenum Certified • RoHS 3• ETL verified to meet the IEC 60512-99-002 standard for support of IEEE 802.3 Type 4 PoE (100 watt) applicationsCOUNTRY OF ORIGINUSA and Mexico (Contact Customer Service for details)6AUJK-xx6, ICONS-ICxUSANetwork Solutions Headquarters +1 (800) 722 2082 *******************Leviton Berk-Tek Cable : +1 (800) 237 5835 ************************Asia Pacific+852 3620 2602********************Canada+1 (800) 461 2002**********************Europe+44 (0) 1592 772124 **********************Latin AmericaMX: +52 (55) 2128 6286 LATAM: +52 (55) 2333 5963 *********************Middle East & Africa +971 (4) 247 9800 *******************NETWORK SOLUTIONS PRODUCTS ARE AVAILABLE WORLDWIDE IN OVER 100 COUNTRIES. VISIT US ONLINE AT /NS TO LEARN MORE.Page 2 of 2For further support information, visit /ns/support6AUJK-xx6, ICONS-ICx6AUJK-xx6, ICONS-ICxMECHANICAL SPECIFICATIONSDimensions:See belowMaterials: Jack Body: Die-cast zincSpring-Wire Contacts: High quality, copper-based alloy, plated with 50 microinches of gold for lowest contact resistance andmaximum life Temp. (Storage):Temp. (Installation): Temp. (Operating):Humidity (Max.):WARRANTY INFORMATIONFor Leviton product warranties, go to /ns/warrantyPART NUMBERDescriptionStandard Jack Jack with Shutter GREENPACK™12-Pack Standard Jack ATLAS-X1™ Cat 6A Component-Rated UTP QUICKPORT™ Jack, white 6AUJK-RW66AUJK-SW66AUJK-CW6ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, light almond 6AUJK-RT66AUJK-ST6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, ivory 6AUJK-RI66AUJK-SI6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, yellow 6AUJK-RY66AUJK-SY6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, orange 6AUJK-RO66AUJK-SO6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, crimson 6AUJK-RC66AUJK-SC6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, dark red 6AUJK-RR66AUJK-SR6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, purple 6AUJK-RP66AUJK-SP6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, blue 6AUJK-RL66AUJK-SL66AUJK-CL6ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, green 6AUJK-RV66AUJK-SV6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, gray 6AUJK-RG66AUJK-SG6—ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, black6AUJK-RE66AUJK-SE66AUJK-CE6ATLAS-X1 Cat 6A Component-Rated UTP QUICKPORT Jack, brown6AUJK-RB66AUJK-SB6—Green (V)Blue (L)Purple (P)Crimson (C)Dark Red (R)Orange (O)Yellow (Y)Black (E)Gray (G)Ivory (I)Light Almond (T)Brown (B)Color-matched icons (ICONS-ICx) can be ordered separately in 72-quantity packs.x = icon color。

鸿怀VM821Q1 AMR 4-Pin 方向编码器 IC 说明书

鸿怀VM821Q1 AMR 4-Pin 方向编码器 IC 说明书

FEATURES• Integrated quadrature sensor IC • Pole size independent operation• 4-pin quadrature, open collector outputs• -40°C to 150°C operating temperature range • Zero speed operation • No calibration required• Insensitive to mechanical vibration• Protection against reverse polarity and short circuit POTENTIAL APPLICATIONS• Industrial speed and direction and position feedback • Encoders• Conveyer rollers speed, process line speed and direction • Gearbox output speed• Positioning roller speed and direction • Garage door opening systems • Induction motors • Fan speed systems• Electric actuated blind position • Pumps and compressors• Integrated seals and bearingsPORTFOLIOThe Honeywell VM821Q1 AMR 4-Pin Quadrature Sensor IC joins the following related products:• VM721D1 AMR 2-Pin PWM Speed and Direction Sensor IC •VM721V1 AMR 2-Pin Speed Sensor ICDESCRIPTIONHoneywell’s Anisotropic Magnetoresistive (AMR) 4-Pin Quadrature Sensor Integrated Circuit (IC) is designed todetect the speed and direction and position of a ring magnet encoder target using a unique* bridge design. The frequency of the output is proportional to the rotational speed of the target, and the rotational direction is encoded by the phase between the outputs. The sensor IC works over a wide range of speeds, temperatures and air gaps.VALUE TO CUSTOMERSThe VM821Q1 sensor IC has a higher sensitivity AMR bridge array that operates with a larger airgap than Hall-effect sensor ICs, which allows for enhanced design flexibility and assembly tolerances. The sensor IC has been optimized to provide an output that is not affected by target runout or sudden air gap changes. It is insensitive to magnet pole size, allowing one sensor to be paired with different ring magnet applications.DIFFERENTIATIONHoneywell’s unique solution utilizes the AMR bridge in saturation, which provides a more stable output response when the system has vibration, sudden air gap changes, or target runout without requiring complex magnitude compensation algorithms. The AMR signal has greatersensitivity than Hall-effect sensor ICs, and does not require automatic gain control or chopper stabilization that can lead to increased jitter over the operating range. *Patent PendingAMR 4-Pin Quadrature Sensor Integrated CircuitVM821Q132336294Issue E23Advanced Sensing TechnlologiesAdvanced Sensing Technologies AMR 4-Pin Quadrature Sensor ICVM821Q1AMR 4-Pin Quadrature Sensor ICVM821Q1Figure 1. Block DiagramNOTICEAbsolute maximum ratings are the extreme limits the device will momentarily withstand without damage to the device. Electrical and mechanical characteristics are not guaranteed if the rated voltage and/or currents are exceeded, nor will the device necessarily operate at absolute maximum ratings.Phase Calculation DefinitionThis method isolates phase from duty cycle. It also best correlates to analysis of the fundamental frequency in the frequency domain.Where:A rising = rising edge of output A A falling = falling edge of output AB rising = nearest falling edge of output B to A rising B falling = next falling edge of output BT = period of one cycleB rising + B falling2Phase (°) =A rising + A falling2-*((360TNOTICELarge, stray magnetic fields in the vicinity of the sensor may adversely affect sensor performance.For more informationHoneywell Advanced SensingTechnologies services its customers through a worldwide network of sales offices and distributors. For application assistance, current specifications, pricing or the nearest AuthorizedDistributor, visit /ast or call:Asia Pacific +65 6355-2828Europe +44 (0) 1698 481481USA/Canada +1-800-537-6945Honeywell Advanced Sensing Technlogies830 East Arapaho Road Richardson, TX /ast4Advanced Sensing TechnlologiesAMR 4-Pin Quadrature Sensor ICVM821Q1Figure 5. Dimensions and Product Marking (For reference only mm/[in])0,80Date code (one digit: 1-9)ADDITIONAL INFORMATIONThe following associated literature is available on the Honeywell web site at :• Installation instructions• Application notes • Technical notes • CAD Models• Evaluation samples available from your local Honeywell contact32336294-E-EN | E | 05/21© 2021 Honeywell International Inc.Product MarkingFigure 4. Sensor IC Mounting OrientationRadialAxialWarranty/RemedyHoneywell warrants goods of its manufacture as being free of defective materials and faulty workmanship during theapplicable warranty period. Honeywell’s standard product warranty applies unless agreed to otherwise by Honeywell in writing; please refer to your order acknowledgment or consult your local sales office for specific warranty details. If warranted goods are returned to Honeywell during the period of coverage, Honeywell will repair or replace, at itsoption, without charge those items that Honeywell, in its sole discretion, finds defective. The foregoing is buyer’s sole remedy and is in lieu of all other warranties, expressed or implied, including those of merchantability and fitness for a particular purpose. In no event shall Honeywell be liable for consequential, special, or indirect damages.While Honeywell may provide application assistancepersonally, through our literature and the Honeywell web site, it is buyer’s sole responsibility to determine the suitability of the product in the application.Specifications may change without notice. The information we supply is believed to be accurate and reliable as of this writing. However, Honeywell assumes no responsibility for its use.。

惠普彩色激光Jet Pro M452dw打印机说明书

惠普彩色激光Jet Pro M452dw打印机说明书

DatasheetHP Color LaserJet ProM452dwIdeal printing performance and robust security for how you work.This capable color printer finishes jobs faster and delivers comprehensive security to guard against threats.1Original HP Toner cartridges with JetIntelligence produce more pages.2Fast printing.Strong protection.●Grab pages and go—without waiting around.This printer wakes up and prints faster than the competition.1●Breeze through multipage documents with two-sided printing that’s faster than leading competitors.1●Protect information and control access to confidential print jobs with HP JetAdvantage Private Print.3●Keep printing safe from boot up to shutdown with security features that guard against complex threats.More.Pages,Performance,and Protection.●Get the most prints for your money—with Original HP High Yield Color Toner cartridges with JetIntelligence.2●Count on professional quality at high speeds with HP ColorSphere 3toner.●Help ensure you’re getting the authentic HP quality you paid for with innovative anti-fraud technology.●Print right away with preinstalled toner cartridges.Replace them with optional high-yield cartridges.Easy management.Efficient printing.●Easily manage print jobs directly at the printer—just tap and swipe the 3-inch (7.6cm)touchscreen.5●Easily print Microsoft®Word and PowerPoint®documents—now directly from your USB drive.4●Easily manage devices and settings using HP Web Jetadmin with a suite of essential management features.6●Print using less energy than competitors—enhanced by Original HP Toner cartridges with JetIntelligence.7Stay connected with easy mobile printing options●Easily print from a variety of smartphones and tablets—generally no setup or apps required.8●Count on wireless direct printing in the office—from mobile devices—without accessing the companynetwork.9●Help workers print with just a touch of their NFC-enabled mobile device to the printer—no network needed.11●Easily access,print,and share resources with Ethernet and wireless networking.10Based on HP internal testing of top three leading competitors’ first page out from sleep mode and duplex print speed completed 8/2015. Subject to device settings. Actualresults may vary. For details see /go/Ljclaims Based on cartridge yields for HP 305X compared with HP 410X Original HP LaserJet Toner Cartridges. For moreinformation, see /go/learnaboutsupplies Feature is only available for the HP Color LaserJet Pro M452dw. HP JetAdvantage Private Print is available at no charge and requires that the printer be connected to the Internet with web services enabled. Not available in all countries. For more information, see Feature is only available for the HP Color LaserJet Pro M452dw. Microsoft and PowerPoint are U.S. registered trademarks of the Microsoft group of companies. Feature works with Microsoft Word and PowerPoint 2003 and later. Only Latin language fonts are supported. Feature is only available for the HP Color LaserJet Pro M452dw. Requires a wireless access point and an Internet connection to the printer. Services require registration. App availability varies by country, language, and agreements and requires a firmware upgrade. For details, visit HP Web Jetadmin is free and available for download at /go/webjetadmin Based on HP testing using the ENERGY STAR® program’s TypicalElectricity Consumption (TEC) method or as reported in of top three leading competitors as of 8/2015. Actual results may vary. For details see /go/Ljclaims Wireless operations are compatible with 2.4 GHz operations only. App or software and HP ePrint account registration may also be required. Some features require purchase of an optional accessory. Learn more at /go/mobileprinting Feature is only supported by the HP Color LaserJet Pro M452nw and M452dw. Mobile device needs to be connected directly to the Wi-Fi network of a wireless direct–capable MFP or printer prior to printing. Depending on mobile device, an app or driver may also be required. Learn more at /go/businessmobileprinting Feature is only supported by the HP Color LaserJet Pro M452nw and M452dw. Wireless performance is dependent on physical environment and distance from access point, and may be limited during active VPN connections. Feature is only supported by the HP Color LaserJet Pro M452dw. Requires a compatible NFC-printing-enabled mobile device. For a list of compatible NFC-printing-enabled mobile devices, see /go/nfcprintingPrint Speed:Black & Color (letter): Up to 28 ppm; First Page Out Time from Ready (Letter): 8.9 seconds (black), 9.5 seconds (color)Print Resolution:Black & color (best): 600 x 600 dpi, Up to 38,400 x 600 enhanced dpiPrint Resolution Technology :HP ImageREt 3600, P ANTONE calibratedStandard Connectivity:Hi-Speed USB 2.0 port; built-in Gigabit Ethernet 10/100/1000 Base-TX network port; Host USBWireless Capability:Yes, Built-in Wi-Fi; Authentication via WEP, WPA/WPA2, WPA Enterprise; Encryption via AES or TKIP; WPS; Wi-Fi Direct Printing; NFC touch-to-Print Standard Memory:256MB NAND Flash, 256MB DRAM Mobile Printing Capability:HP ePrint, Apple AirPrint™,Wireless Direct Printing, NFC touch-to-print, Mopria-certified, Google Cloud Print, Mobile AppsPaper Handling:50-sheet multipurpose tray, 250-sheet input tray; 150-sheet output bin; Optional 550-sheet input trayDisplay:3.0-in intuitive color touchscreenDatasheet|HP Color LaserJet Pro M452dwHP Color LaserJet Pro M452dw Specifications TablePrint Speed Letter:Up to28ppm black;Up to28ppm color14First Page Out:As fast as8.9sec black;Asfast as9.5sec color (ready); As fast as 11.3 sec black; As fast as 11.4 sec color (sleep)16 Print Resolution Black(best):600x600dpi,Up to38,400x600enhanced dpi;Color(best):600x600dpi,Upto38,400x600enhanced dpiPrint Technology LaserPrint Resolution Technologies HP ImageREt3600,P ANTONE calibratedPrint Cartridges Number4(1each black,cyan,magenta,yellow)Standard Print languages HP PCL6,HP PCL5c,HP postscript level3emulation,PDF,URF,PCLm,Native Office,PWGRasterPrinter Smart Software Features N-up printing,collation,HP ePrint,Apple AirPrint™,Mopria certified,Google Cloud Print,NFCtouch-to-print,wireless direct printing,HP Auto-On/Auto-Off Technology,Intiutive3"touchscreen control panel,Print from Cloud using business apps on the control panel,HPJetAdvantage Private Print,Job Storage with PIN printing,Print from USBPrinter Management Printer Administrator Resource Kit(Driver Configuration Utility,Driver Deployment Utility,Managed Printing Administrator);HP Web JetAdmin Software;HP Proxy Agent Software;HPImaging and Printing Security Center;HP Utility(Mac);HP Device Toolbox(Win7)Standard Connectivity Hi-Speed USB2.0port;built-in Gigabit Ethernet10/100/1000Base-TX network port;Host USBNetwork Capabilities Via built-in10/100/1000Base-TX Ethernet,Gigabit;Auto-crossover Ethernet;Authenticationvia802.1XNetwork Ready Standard(built-in Gigabit Ethernet,Wi-Fi)[Operates as both an AP(with Wi-Fi Direct)and STA] Wireless Capability Yes,Built-in Wi-Fi;Authentication via WEP,WPA/WPA2,WPA Enterprise;Encryption via AES orTKIP;WPS;Wi-Fi Direct Printing;NFC touch-to-PrintMobile Printing Capability HP ePrint,Apple AirPrint™,Wireless Direct Printing,NFC touch-to-print,Mopria-certified,Google Cloud Print 2.0,Mobile AppsMemory Standard:256MB NAND Flash,256MB DRAM;Maximum:256MB NAND Flash,256MB DRAM Processor Speed1200MHzDuty Cycle Monthly,letter:Up to50,000pages7Recommended Monthly Page Volume750to4,0008Media Types Supported Paper(bond,brochure,colored,glossy,letterhead,photo,plain,preprinted,prepunched,recycled,rough),postcards,labels,envelopesMedia Weight Supported Tray1:16to47lb(up to52lb with HP Color laser glossy photo papers);Tray2:16to43lb(upto47lb with postcards,up to52lb with HP Color laser glossy photo papers);optional Tray3:16to43lb(up to47lb with postcards,up to40lb with HP Color laser glossy photo papers);Automatic duplexer:16to43lbMedia Sizes Supported Tray1,Tray2:Letter,legal,executive,Oficio(8.5x13in),3x5in,4x6in,5x8in,envelopes(No10,Monarch);Optional Tray3:Letter,legal,executive,Oficio(8.5x13in),3x5in,4x6in,5x8in;Automatic duplexer:Letter,legal,executive,Oficio(8.5x13in)Media Sizes Custom Tray1:3x5to8.5x14in;Tray2,optional Tray3:3.94x5.83to8.5x14inPaper Handling50-sheet multipurpose tray,250-sheet input tray;150-sheet output bin;Duplex Options:Automatic(standard);Envelope Feeder:No;Standard Paper Trays:2;Input Capacities:Up to300sheets;Output Capacities:Up to150sheets;Up to20envelopesWhat's in the box CF394A HP Color LaserJet Pro M452dw;4preinstalled Introductory HP410A LaserJetToner cartridges(Black,Cyan,Magenta,Yellow:~1200pages);In-box documentation(Getting Started Guide, Install Poster); Software drivers and documentation on CD-ROM;Power cord; USB cable; Built-in duplexerReplacement Cartridges HP410A Black LaserJet Toner Cartridge(~2300pages)CF410A;HP410X Black LaserJet TonerCartridge(~6500pages)CF410X;HP410A Cyan LaserJet Toner Cartridge(~2300pages)CF411A;HP410X Cyan LaserJet Toner Cartridge(~5000pages)CF411X;HP410A YellowLaserJet Toner Cartridge(~2300pages)CF412A;HP410X Yellow LaserJet Toner Cartridge(~5000pages)CF412X;HP410A Magenta LaserJet Toner Cartridge(~2300pages)CF413A;HP410X Magenta LaserJet Toner Cartridge(~5000pages)CF413X5Product Dimensions W x D x H:16.2x18.5x11.6in11;Maximum:16.2x25.6x13.4inProduct Weight41.7lb1Warranty Features One-year,Bench Repair limited warrantyEnergy Efficiency Compliance ENERGY STAR®certified;Blue Angel;EPEAT®SilverControl Panel 3.0-in intuitive color touchscreen;3Buttons(Home,Help,Back)Display Description 3.0-in intuitive color touchscreenSoftware Included For Windows OS:HP Software Installer/Uninstaller,HP PCL6Printer Driver,HP DeviceExperience(DXP),HP Update,Product Registration Assist,HP Web Services Assist(HPConnected),HP Device Toolbox,HP Product Improvement Study,Online user manuals.(Software varies by OS:WinXP/Vista=driver only);Windows7:Full solution;Windows8+andnewer:drivers only with more apps availabe in MS App store;For Mac OS:Welcome Screen,(Directs users to or OS App Source for LaserJet Software)Fonts and Typefaces84scalable TrueType fontsCompatible Operating Systems Windows OS compatible with In-Box Driver:Windows XP SP3all32-bit editions(XP Home,XPPro,etc),Windows Vista all32-bit editions(Home Basic,Premium,Professional,etc),Windows7all32-&64-bit editions,Windows8/8.1all32-&64-bit editions(excluding RT OS forTablets),Windows10all32-&64-bit editions(excluding RT OS for Tablets);Windows OScompatible with Universal Print Driver(From ):Windows XP SP332-&64-bit editions(XP Home,XP Pro,etc),Windows Vista all32-&64-bit editions(Home Basic,Premium,Professional,etc),Windows7all32-&64-bit editions,Windows8/8.1all32-&64-bit editions(excluding RT OS for Tablets),Windows10all32-&64-bit editions(excluding RT OS forTablets);Mac OS(HP Print Drivers available from and Apple Store):OS X10.7Lion,OS X10.8Mountain Lion,OS X10.9Mavericks,OS X10.10Yosemite;Mobile OS(In-OS drivers):iOS,Android,Windows8/8.1/10RT;Linux OS(In-OS HPLIP);SUSE Linux(12.2,12.3,13.1);Fedora(17,18,19,20);Linux Mint(13,14,15,16,17);Boss(3.0,5.0);Ubuntu(10.04, 11.10, 12.04,12.10, 13.04, 13.10, 14.04, 14.10); Debian (6.0.x, 7.x); Other OS: UNIX Compatible Network OperatingSystemsWindows OS compatible with In-Box Driver:Windows Server2003/2003R232-bit(SP1/SP2)Standard/Enterprise(+Cluster&Terminal Services),Windows Server200832-/64-bit(SP2)Standard/Enterprise(+Cluster&Terminal Services),Windows Server2008R264-bit(SP1)Standard/Enterprise(+Cluster&Terminal Services);Windows OS compatible with UniversalPrint Driver(UPD)or Product-Specific drivers from :Windows Server2003/2003R232-/64-bit(SP1/SP2)Standard/Enterprise/Datacenter(+Cluster&Terminal Services),Windows Server2008/2008R232-/64-bit(SP1/SP2)Standard/Enterprise/Datacenter(+Cluster&Terminal Services),Windows Server2012/2012R264-bitStandard/Foundation/Essentials/Datacenter(+Cluster&Terminal Services);Citrix(on WindowsServer2003/2003R2):Citrix MetaFrame Presentation Server,3.0,Citrix MetaFrame XPPresentation Server(Feature Release1,2,and3),Citrix Presentation Server4.0/4.5,CitrixXenApp5.0(Plus Feature Pack2&3);Citrix(on Windows Server2008/2008R2):Citrix XenApp5.0(Plus Feature Pack2&3),Citrix XenApp6.0/6.5/7.5,Citrix XenDesktop5.6/7.0/7.5;Citrix(on Windows Server2012/2012R2):Citrix XenApp7.5,Citrix XenDesktop7.0/7.5;NovellServers(/iprint):Novell iPrint Appliance v1.0,Novell Open EnterpriseServer11/SP1,Novell Open Enterprise Server2for Linux;NetWare6.5/SP8;Novell Clients(/iprint);Windows8(32-bit/64-bit)recommend v5.86+,8.1recommend v5.94+,Windows7(32-bit/64-bit)recommend v5.82+,Windows Vista(32-bit/64-bit)recommend v5.82+,Windows XP/SP3(32-bit only)recommend v5.82+ Minimum System Requirements PC:Windows XP(SP2)(32-bit)or newer;233MHz processer or higher;512MB RAM;400MBavailable hard disk space;CD-ROM or Internet;USB or Network connection;MAC:Mac OS X v10.7or newer;Internet;USB or Network connection;1GB available hard disk spacePower Power Supply Type:Internal(Built-in)power supply;Power Requirements:110-volt inputvoltage:110to127VAC(+/-10%),60Hz(+/-3Hz);220-volt input voltage:220to240VAC(+/-10%),50Hz(+/-3Hz)(Not dual voltage,power supply varies by part number with#Option code identifier);Typical Electricity Consumption:1.515 kWh/Week; PowerConsumption: 570 watts (Active Printing), 17.6 watts (Ready), 2.4 watts (Sleep), 0.6 watts(Auto-On/Auto-Off, via USB connectivity), 0.05 watts (Shutdown or Off)Acoustics Acoustic Power Emissions(active):6.3B(A);Acoustic Power Emissions(ready):4.8B(A);Acoustic Pressure Emissions(active):49dB(A);Acoustic Pressure Emissions(ready):34dB(A)6Operating Environment Operating Temperature Range:59to86°F;Recommended Operating Temperature:59to80.6°F;Storage Temperature Range:-4to104°F;Non-Operating Humidity Range:10to95%RH(non-condensing);Operating Humidity Range:10to80%RH(non-condensing);Recommended Humidity Operating Range:20to70%RH(non-condensing)Security Management Embedded Web Server:password-protection,secure browsing via SSL/TLS;Network:enable/disable network ports and features,SNMPv1&SNMPv2community password change;HP ePrint:HTTPS with certificate validation,HTTP Basic Access Authentication,SASLauthentication;Firewall and ACL;SNMPv3,802.1X,Secure Boot,authentication via WEP,WPA/WPA2Personal,WPA2Enterprise;Encryption via AES or TKIPAccessories HP LaserJet550-sheet Paper Feeder CF404A;HP v222w16GB Mini USB Drive P0R81AAHP Service and Support Options U8TN1E-HP3year Next Business Day Color LaserJet M452Hardware Support;U8TN2E-HP4year Next Business Day Color LaserJet M452Hardware Support;U8TN3E-HP5year NextBusiness Day Color LaserJet M452Hardware Support;U8TN4E-HP3year Next Business DayExchange Color LaserJet M452Service;H3110E-HP Network Install Inkjet/Personal LaserJetServiceLearn more atWith toner cartridges.Power requirements are based on the country/region where the printer is sold. Do not convert operating voltages. This will damage the printer and void the product warranty.Typical Electricity Consumption(TEC)rating represents the typical electricity consumed by a product during1week,measured in kilowatt-hou r s(kWh).Printer ships with preinstalled introductory cartridges Cyan,Magenta and Yellow(CMY)(~1200pages)and Black A(KA)(~2300pages)with Auto Toner Seal Removal for all cartridges. Acoustic values are subject to change.For current information see /support.Configuration tested:base model,simplex printing,A4paper at an average of20ppm.Duty cycle is defined as the maximum number of pages per month of imaged output.This value provides a comparison of product robustness in relation to other HP LaserJet or HP Color LaserJet devices,and enables appropriate deployment of printers and MFPs to satisfy the demands of connected individuals or groups.HP recommends that the number of printed pages per month be within the stated range for optimum device performance,based on factors including supplies replacement intervals and device life over an extended warranty period.Not all"Compatible Operating Systems"are supported with inbox software;Full solution software available only for Windows7;Legacy Windows Operatin g Systems(XP,Vista,and equivalent servers)get print and Scan drivers only;Windows8and10have apps available in MS App Store;Windows RT OS for Tablets(32-&64-bit)uses a simplified HP print driver built into the RT OS;UNIX modelscripts are available on (Modelscripts are printer drivers for UNIX operating systems);Linux systems use in-OS HPLIP software Without optional550-sheet tray.Dimensions with optional550-sheet tray:16.2x18.5x16.7in (412x469x425mm). Measured using ISO/IEC 24734, excludes first set of test documents. For more information see /go/printerclaims. Exact speed varies depending on the system configuration, software application, driver, and document complexity.Measured using ISO/IEC 17629. For more information see /go/printerclaims. Exact speed varies depending on the input voltage, system configuration, software application, driver, and document complexity. Declared cartridge yield value in accordance with ISO/ IEC 19752. Actual yields vary considerably based on images printed and other factors. For more information, visit /go/learnaboutsupplies. HP Color LaserJet Pro M452 in-box cartridge may have higher yield than stated for printer units manufactured before 2017.©Copyright2015HP Development Company,L.P.The information contained herein is subject to change without notice.The only warranties for HP products and services are set forth in the express warranty statements accompanying such products and services.Nothing herein should be construed as constituting an additional warranty.HP shall not be liable for technical or editorial errors or omissions contained herein.ENERGY STAR and the ENERGY STAR logo are registered U.S.marks.Windows is a registered trademark of Microsoft Corporation.AirPrint,iPad,iPhone,and iPod touch are trademarks of Apple Inc.,registered in the U.S.and other countries.c04743696, August 2015。

阿特拉斯枪样本

阿特拉斯枪样本
工业动力装配工具及系统
全球领先的工业生产力解决方案
2008-2009
内容
气动装配工具
11
选择向导 – 气动装配工具................................................... 12 工具代码............................................................................. 14 气动冲击扳手...................................................................... 17 油压脉冲拧紧扳手 – EP...................................................... 22 带监测功能的脉冲工具 – Pulsor......................................... 30 螺丝刀................................................................................. 33 气动扳手............................................................................. 44 弯头式扳手......................................................................... 45 直柄式扳手......................................................................... 57 手枪式扳手......................................................................... 62

7777型号选择指南:Meredian II电极线性或浸湿装配说明书

7777型号选择指南:Meredian II电极线性或浸湿装配说明书

51-52-16U-17Issue 29Page 1 of 3Series 7777Model Selection GuideMeredian® II ElectrodeIn-Line or Immersion MountingKEY NUMBERSelectionAvailabilityDescription7777 Electrode Mounting07777In-line mountingTee not includedTABLE II - Mounting, Leads, Instrument Connection, Part No.Meredian II Glass pH:Mounting Leads (Integral)Instrument Connection P/NIn-Line Quick Disconnect Direct Connection to:09c (Note 3)UDA2182, APT2000/4000Immersion20' Tinned c (6,10 meters)In-Line18c Immersion12' (6 pin preamp connector)03d (3,66 meters)In-Line14dORP Electrodes:Mounting LeadsTemp.In-LineQuick Disconnect11c (Note 3)12c Immersion 20' Tinned -5 to 110oC07c (6,10 meters) -5 to 110oC08c In-Line20' Tinned -5 to 110oC27c (6,10 meters) -5 to 110oC28c 50' Tinned 29c(15,25 meters)RESTRICTIONSRestrictionLetter Table Selection Tablec I 0d I3Note 1:For longer preamp to instrument cables, see Accessories and Spare Parts List.Note 2: Gold is generally used in applications containing cyanide; platinum is used for all others.Note 3:Please order corresponding Quick Disconnect sensor-to-instrument cable from accessory table.50027820-502 (gold)16Available Only With51451341-504 (gold) 51451326-50431074387-501 -5 to 110oC 51451340-505 (platinum)50027820-501Not Available With31074399-50151451340-503 (platinum) 51451340-504 (platinum) -5 to 110oC-5 to 110oC50027820-503 (platinum)Selection51451341-503 (gold) P/N (Note 2)Direct Connection to:51451326-503Preamp Connection UDA2182, APT2000/4000Series 7777Accessories andReplacement PartsDescription Part NumberDirections - Meredian II Mounting70-82-25-05Directions - Preamp (31075704-501 & 31075705-501)70-82-25-57Directions - Meredian II Electrode70-82-25-56pH Buffer Solutions4.0131103001-5016.8631103002-5019.1831103003-501Extension Cables for Sensors with Quick Disconnect Option:2m (6.56 Ft.)50024092-5013m (9.84 Ft.)50024092-5026m (19.69 Ft.)50024092-503Only Honeywell Extension Cables can be used.Cable - preamp to instrumentTable I = 3 - 20 feet (6,10 meters)31075723-501- 50 feet (15,25 meters)51309677-501Smooth Electrode Tip - In-Line Mounting31074331-501Guarded Electrode Tip - Immersion Mounting31074330-501Frit 0-Ring (for replacement tips)31074365-501Junction Box50034477-501Special CPVC pipe tee for 3/4" in-line mounting31120167-501Cable grip - for Meredian glass and preamp to instrument cables (3/4" NPT31074354-501 connection and 0.25" grommet hole)。

超导磁共振氦压缩机结构功能与故障案例分析

超导磁共振氦压缩机结构功能与故障案例分析

维修工程中国医学装备2024年4月第21卷第4期 China Medical Equipment 2024 April V ol.21 No.4Structural function and failure case analysis of superconducting magnetic resonance helium compressor/Zhang Falun 1, Wang Jixi 2, Zhou Yalin 2, Shi Zhan 31Department of Medical Equipment T eaching and Research, Jiangsu Health V ocation College, Nanjing 211800, China; 2Department of Medical Engineering, Jiangsu Province Official Hospital, Nanjing 210024, China; 3Siemens Medical Systems Ltd., Shanghai 201318, ChinaCorresponding author: [Abstract] Helium compressor is the core component of the refrigeration system of superconducting magnetic resonance imaging (MRI) equipment, and timely resolution of helium compressor failures is crucial to ensure the stability of the superconducting magnet cryogenic system. T aking the Sumitomo F-70 helium compressor manufactured by Sumitomo Heavy Industries as an example, the structural composition and functional principle of the helium compressor for superconducting MRI were analyzed, and the maintenance ideas and solutions for common helium compressor faults were proposed. By developing standardized fault maintenance strategies, reference was provided for failures of other types of helium compressor, so as to improve the quality of clinical technical support.[Key words] Superconducting magnetic resonance imaging; Helium compressor; Structure and function; Fault diagnosisFund program: 2022 Faculty Research Projects of Jiangsu Health V ocation College (JKC2022006)[摘要] 氦压缩机是超导磁共振成像(MRI)设备制冷系统核心部件,及时解决氦压缩机故障对保障超导磁体低温系统的稳定性至关重要。

大众发动机

大众发动机

Petrol engines[edit]EA 111The EA111 series was introduced in the mid 1970s in the Audi 50 and later the VW Polo. It is a series of water cooled three- and four-cylinder petrol and Diesel engines in a variety of sizes. The overhead cam engine features a crossflow cylinder head design and directly-driven auxiliary units. The exhaust side is in driving direction.[edit]Three cylinders[edit]55-70 hp 1.2configurationwater cooled 1198 cm³ inline threehead(2 V) aluminium, SOHC, two valves per cylinder, 10.3:1 compression(4 V) aluminium, DOHC, four valves per cylinder, 10,5:1 compression ratioblockaluminium, four bearings, balancer shaft, 76.5 mm bore × 86.9 mm stroke, 0.88 ratio, 399 cm³ per cylinderfuelelectronic injectionoutput(2 V) 40 kW (55 hp) at 4750 rpm, 108 N·m (80 ft·lbf) at 3000 rpm(4 V) 47 kW (64 hp) at 5400 rpm, 112 N·m at 3000 rpm(4 V) 51 kW (70 hp) at 5400 rpm, 112 N·m at 3000 rpmapplicationVW Fox, VW Polo (PQ 24) and Skoda FabiareferencesVW AG (2005-04-04). New VW Fox In Depth. Press release.[edit]68-90 hp 1.2FSIconfigurationwater cooled 1198 cm³ inline threeheadaluminium, DOHC, four valves per cylinder, 12.3:1 compressionblockaluminium, four bearings, balancer shaft, 76.5 mm bore × 86.9 mm stroke, 0.88 ratio, 399 cm³ per cylinder fuelFSI direct petrol injection, up to 150 bar high-pressure pump and common railaspirationmulti-position tumble flap in the intake port controlling the tumble effectexhaustup to 25% cooled exhaust gas recirculationoutput50 kW (68 hp) at 5000 rpm, 115 N·m (80 ft·lbf) at 3250 rpm65 kW (89 hp) at 6000 rpm, 120 N·m at 3500 rpmapplicationVW Polo PQ 25[edit]Four cylinders[edit]70 hp 1.0configurationbore/stroke 67,1/70,6 mm 0.95 ratio, 249 cm³ per cylinder, 999 cm³ inline fourheadaluminium, SOHC, two valves per cylinder, 10.8:1 compressionblockaluminium, five bearingsfuelelectronic injection Total Flex Gasoline or Ethanol (BR)output (2 V)51 kW (70 PS) at 5750 rpm, 90 N·m (65 ft·lbf) at 4250 rpmapplicationVW Fox[edit]75 hp 1.4configurationbore/stroke 76,5/75,6 mm, 1.01 ratio, 347,5 cm³ per cylinder 1390 cm³ in line fourheadSOHC 2-valve per cylinder, 10.5:1 compressionblockcast iron, five bearingselectronic injectionoutput55 kW (75 hp) at 4800-5000 rpm, 124 N·m (92 ft·lbf) at 2750 rpmapplicationVW Fox, VW Kombi (T2) in Brasil[edit]75-100 hp 1.41.4 engine cutawayconfiguration76.5 bore × 75.6 mm stroke, 1.01 ratio, 347.5 cm³ per cylinder, 1390 cm³ inline fourheadaluminium, DOHC, four valves per cylinder, 10.5:1 compressionblockaluminium, five bearingsfuelelectronic injection MPi Gasolineoutput55 kW (75 PS) at 5000 rpm, 126 N·m (93 ft·lbf) at 3800 rpm, only assemled with the 4-Gear automatic and in Skoda Cars59 kW (80 PS)- 63 kW (86 PS) at 5000 rpm, 128-132 N·m (98 ft·lbf) at 3300-3800 rpm74 kW (100 PS) at 6000 rpm, 126 N·m (93 ft·lbf) at 4400 rpm, no longer assembled in western europeapplicationVW Polo,VW Golf,SEAT León,Skoda Roomster,Skoda Fabia[edit]86-105 hp 1.4FSIconfiguration76.5 bore × 75.6 mm stroke, 1.01 ratio, 347.5 cm³ per cylinder, 1390 cm³ inline fourheadaluminium, DOHC, four valves per cylinder, 12:1 compressionaluminium, five bearingsfuelFSI direct petrol injection, up to 110 bar high-pressure pump and common rail, stratified-charge combustion at partial load aspirationtwo-position tumble flap in the intake port controlling the turbulenceexhaustup to 35% exhaust gas recirculation, NOx storage-type catalytic convertermanagementBosch Motronic MED7output63 kW (86 PS) at 5000 rpm, 130 N·m (95 ft·lbf) at 3750 rpm in VW Polo66 kW (90 PS) at 5200 rpm, 130 N·m (95 ft·lbf) at 3750 rpm in VW Golf (-05/05)77 kW (105 PS) at 6200 rpm, 131 N·m (96 ft·lbf) at 4250 rpm in VW Lupo FSI[edit]140/170 hp 1.4 TSIVolkswagen 1.4 TSI engine exploded viewVolkswagen 1.4 TSI engine operation schemeAnnounced at the 2005 Frankfurt Auto Show to be used in the Golf GT, The 1.4l Twincharger is a TSI engine with a turbocharger and a supercharger in combination. Its downsizing leads to economy, with 14% more power than the 2.0 FSI but consumming 5% less fuel. The mechanical compressor operates at low engine speeds below 2400 rpm to increase low-end power, the turbocharger engages at middle revs, a clutch disengage the supercharger which will then be bypassed once the turbocharger reaches sufficient speed to provide boost above 3500 rpm.Configuration1390 cm³straight-4Headfour-valve, 10:1 compression ratioBlockgrey cast iron, bore * stroke ratio 76.5 * 75.6 mm, 120 bar peak pressuresFuelFSI direct petrol injection up to 150 bar, high-pressure injection multiple-hole valve with six fuel outlet elements, injector on the intake side between the intake port and cylinder head seal levelAspirationmechanical belt driven Roots compressor operated by a magnetic clutch integrated in a module inside the water pump, internal step-down ratio on the input end of the synchronisation gear pair and exhaust turbocharger connected in series, administrated by a control flap, intercooler, 2.5 bar pressure at 1500 rpm.Output103 kW (140 PS), 220 N·m in the Touran from early 2006125 kW (170 PS) at 6000 rpm, 240 N·m (MEP 21.7 bar) from 1750 to 4500 rpm , 200 N·m from 1250 to 6000 rpm, 7000 rpm max in the Golf GTApplications2005 VW Golf, 2006 VW Touran, 2008 VW Scirocco, possibly in the 2008 VW Concept RReferencesV olkswagen AG (2005-08-29). Volkswagen Golf GT TSI - Supercharged and Turbocharged 1.4l. Press release.[edit]100-105 hp 1.6configuration76.5 bore × 86.9 mm stroke, 0.88 ratio, 399 cm³ per cylinder, 1598 cm³ in line fourheadDOHC 4-valve per cylinder, 10.5:1 compressionSOHC 2-valve per cylinder, 10.6:1 compression (BR)blockaluminium alloy, five bearingscast iron, five bearings (BR)fuelelectronic multipoint injection Bosch MD7electronic injection Total Flex Gasoline or Ethanol (BR)output77 kW (105 PS) at 5600 rpm, 153 N·m (115 ft·lbf) at 3800 rpm74 kW (101 PS) at 5500 rpm, 141 N·m (106 ft·lbf) at 3200 rpm (BR)applicationVW Fox, VW Polo, VW Golf in Model 2006, including 6-Gear-Automatic[edit]115 hp 1.6 FSI1.6 FSI engine cutaway1.6 FSI exploded viewConfiguration1598 cm³ inline fourheadaluminium, DOHC chaindrive, variable intake camshaft timing, four valves per cylinder, 12:1 compressionblockaluminium alloy, five main bearings, 76.5 mm Bore × 86.9 mm stroke (0.88 ratio), 399.5 cm³ per cylinderfuelGasoline, Fuel Stratified Injection, up to 110 bar high-pressure pump and common rail, stratified-charge combustion at partial loadaspirationtwo-position tumble flap in the intake port controlling the turbulenceexhaustup to 35% exhaust gas recirculation, NOx storage-type catalytic convertermanagementBosch Motronic MED7output85 kW (115 hp) at 5800-6000 rpm, 155 N·m at 4000 rpmapplicationsVW Golf, VW Jetta, VW Touran, VW Passat, Audi A2, Audi A3, Audi A4, Škoda OctaviaReferencesAudi AG (2001-03-10). Audi A2 1.6 FSI with Direct Petrol Injection. Press release.[edit]EA113 / 827The EA827 family was introduced in 1972 in the Audi 80 and eventually superseded by the EA113 evolution introduced in 1993. Both share the same 88 mm cylinder spacing. It was later updated with direct injection, to be topped by the 265 PS 2.0L TFSI. 40 million engines have been produced. It was replaced by the EA888 project introduced with the 1.8L TFSI below.[edit]102 hp 1.6configuration1595 cm³ (97 in³) inline 4headSOHC 2-valve per cylinder, 10.3:1 compressionDOHC 5-valve per cylinder, 10.5:1 compression (China)blockaluminium, five bearings, bore 81 × stroke 77.4 mm, 1.05 ratio, 399 cm³ per cylinderoutput75 kW (102 hp) at 5600 rpm, 148 N·m (109 ft·lbf) at 3800 rpm80 kW (109 hp) at 5800 rpm, 150 N·m (111 ft·lbf) at 4200 rpm (China)applicationsSkoda OctaviaV olkswagen Jetta (China)[edit]90-109 hp 1.8configuration1781 cm³ inline 4, : bore 81 × stroke 86.4 mmheadSOHC 2-valve per cylinder, 10.8:1 compressionblockcast iron engine block, five bearingsfuelelectronic singlepoint injection Bosch Motoronicelectronic injection Total Flex Gasoline or Ethanol (BR)output66 kW (90 hp) at 5500 rpm, 145 N·m (108 ft·lbf) at 2500 rpm in VW Gol, VW Pointer (MX)76 kW (103 hp) at 5400 rpm, 155 N·m (112 ft·lbf) at 3000 rpm in VW Gol, VW Santana, VW Saveiro (BR, MX, AR) [edit]150-240 hp 1.8 TAudi AG (02-22-2005). Audi TT quattro sport Revealed. Press release.[edit]115/130 hp 2.0Audi 2.0 20 valves engine cutawayconfiguration1984 cc (121 in³)blockbore 82.5 × stroke 92.8 mm, cast ironheadaluminum, SOHC, 2 valves per cylinder with bucket tappets, one-piece cast camshaft, compression ratio 10.0:1 crankcaseforged steel connecting rodsaspirationcast aluminum intake manifoldengine managementMotronic, regular unleaded fueloutput86 kW (115 hp) at 5200 rpm, 165 N·m (122 ft·lbf) at 2600 rpm85 kW (115,5 hp) at 5400 rpm, 172 N·m (125 ft·lbf) at 3500 rpm in VW Passat80 KW (109 hp) at 5400 rpm, 160 Nm (120 ft. lbf) at 3500 rpm in Ecofuel Touran or Caddy96 kW (130 hp) at 5700 rpm, 195 N·m at 3300 rpm with five valves per cylinder, continuous intake camshaft adjustment, atwo-position variable intake manifold and a balancer shaft in the Audi A4applicationsVW Golf, VW Jetta, Jetta Wagon, VW New Beetle, Skoda Fabia[edit]150 hp 2.0 FSI2.0 FSI cutaway drawingEngine codeBPGconfiguration1984 cm³ inline fourblock82.5 bore x 92.8 strokeheadDOHC, compression ratio 11.5:1, continuously adjustable intake camshaft, four valves per cylinder actuated by low-friction roller cam followersfuelGasoline, Fuel Stratified Injection, single-piston high-pressure injection pump, air-guided combustion process, stratified and homogeneous lean operation with excess air at part loadaspirationvariable intake manifold and dual-branch front pipeoutput110 kW (150 hp) at 6000 rpm, 200 N·m at 3500 rpmapplicationsVW Golf, VW Passat, Audi A3, Audi A4, Skoda Octavia, SEAT León, SEAT Toledo, SEA T AlteareferencesAudi AG (2004-07-19). Audi A3 Sportback – In Depth. Press release.[edit]170-265 hp 2.0 TFSI I4Engine codeBPYConfiguration1,984 cc water cooled inline 4, based on the naturally aspired 2.0 FSICylindersbore × stroke 82.5 × 92.8 mm (0.89 rati), 496 cc/cylinder, 10.5:1 compression ratioBlockCG 25 grey cast iron, 88 mm cylinder spacing, two chain driven balancing shaftsHeadfour-valve, low-friction roller cam follower drive, modified inlet duct geometry for high tumble values providing superior knock resistance, continuous intake camshaft adjustmentFuel systemGasoline, Fuel Stratified Injection, up to 110 barAspiration0.9 bar boost turbocharger, intercooler, variable plastic controlled intake manifold with charge movement flaps adjusted by acontinuous-action pilot motordimensions652 mm long, 648 mm wide, 666 mm high, 152 kgOutputeight counterweights, 58 mm diameter main bearingsFuel systemGasoline, Fuel Stratified Injection, up to 150 bar, six-hole injectors, high-pressure pump driven by a four-fold cam on the exhaust camshaft, stainless steel high-pressure lines, dual injection at the admission and compression strokeAspirationBorg Warner K03 watercooled turbocharger, intercooler, charge movement flaps controlling combustion chamber air movementexhaustceramic primary catalytic converter and ceramic close-coupled catalytic converterOutput118kW (160 PS) from 5,000 to 6,200 rpm, 250 Nm from 1,500 to 4,200 rpm, 165 Nm at 1,000 rpmapplication2006, Audi A3ReferenceAudi AG (2006-09-27). Sporty Dynamism, Superb Comfort: The Audi 1.8 TFSI. Press release.[edit]Five cylinder[edit]150/170 hp 2.3 VR5configurationwater cooled 2324 cm³VR5headaluminium, DOHC, four valves per cylinder, 10.8:1 compressionblockcast iron, wet sumped, six bearings, 81 mm bore × 90.2 mm stroke, 0.9 ratio, 465 cm³ per cylinderaspirationvariable intake manifold, tubular exhaust manifoldfuelelectronic injectionoutput125 kW (170 hp) at 6200 rpm, 220 N·m (162 ft·lbf) at 3300 rpm from 2001110 kW (150 hp) at 6000 rpm, 209 N·m (154 ft·lbf) at 3200 rpm from 1997applicationsVW New Beetle, VW Golf, VW Bora, VW Passat[edit]150 hp 2.5 (US)configuration2480 cc (151 in³) inline 5blockbore 82.5 × stroke 92.8 mm, cast ironheadaluminum, [DOHC], 4 valves per cylinder actuated by low-friction roller cam followers, build camshafts, intake camshaft adjustmentcrankcasealuminiumaspirationcast aluminum two-position variable intake manifoldengine managementMotronic, regular unleaded fueloutput110 kW (150 hp) at 5000 rpm, 225 N·m (170 ft·lbf) at 3750 rpmapplicationRabbit, Jetta, New Beetle for the North American Market as the replacement for the 2.0 L4[edit]Six cylinder[edit]177 hp 2.4 V6Audi 2.4L V6 FSI cutaway drawingThe 2.4 V6 is a smaller version of the 3.2 FSI without the variable intake manifold and the FSI direct injection.Engine codeBDVConfiguration2393 cm³ 90°V6CylindersBore × stroke 81 mm × 77.4 mm (0.91 ratio), 399 cm³/cylinder, aluminium blockCrankshaftaluminiumHeadsaluminium, 4 valves per cylinder, DOHC, 11.3:1 Compression ratio, chain driven camshafts, continuously variable valve timing system both for intake and exhaustFuel systemMotronic ME 7.X electronic sequential SFI fuel injectionExhausttwo ceramic catalytic convertersOutput130 kW (177 hp) @ 6000 rpm (15.5 m/s piston speed), 230 N·m between 3000 and 5000 rpm (12.1 bars MEP)Application2004 Audi A6referencesAudi AG (2004-04-08). New Audi A6 In Depth. Press release.[edit]210 hp 2.8 V6 FSIAudi 2.8L V6 FSI cutaway drawingThe 2.8 V6 is a stroke-reduced version of the 3.2 FSI introducing the valvelift variable control of inlet valve lift.Configuration2773 cm³ 90°V6, 18.5 mm cylinders banks offsetCylindersBore × stroke 84.5 × 82.4mm (1.03 ratio), 462 cm³/cylinderCrankcase360 mm long, 430 mm, 228 mm high, 33 kg, low-pressure die-casting, hypereutectic aluminium alloy, 17% silicon, 4% copperHeads4 valves per cylinder, DOHC, 12:1 compression ratio, continuously variable valve timing system both for intake and exhaust,valvelift inlet valve lift variable controlFuel systemFSI petrol direct injectionDimensions165 kgOutput154 kW (210 PS) at 5,500 rpm, 280 Nm from 3,000 to 5,000 rpm, 6,800 rpm maxApplication2006, Audi A6referencesAudi AG (2006-09-27). The New 2.8 FSI with Audi Valvelift System. Press release.[edit]194 hp 2.8 V6Engine codeAHA/ATQ (2.7T: APB)configuration2771 cm³ water cooled V6, bore 82.5 mm × 86.4 mm strokeheadDOHC, 5 valves per cylinder, 30 valves total, compression ratio 10.6:1output194 hp (142 kW) @ 6000 rpm, 280 N·m (206 ft·lbf) @ 3200 rpmengine managementMotronic, regular premium unleaded fuelapplicationsVW Passat including the Variant and Škoda Superb; Audi A4, Audi A6 and Audi A8 in a 30 valves version. [edit]204 hp 2.8 VR6201 hp 2.8L VR6 cutawayconfiguration2792 cc Wet sumped 15°VR6headaluminium, DOHC, 4 valves per cylinder, 24 valves total, compression ratio 10.7:1blockcast iron, 7 main bearings, bore 81 × stroke 90.3 mm (ratio 0.9), 465 cc per cylinderfuel systemMotronic ME7.1, MPFi, regular premium unleaded (91 AKI)output150 kW (204 hp) @ 6200 rpm, 265 N·m (195 ft·lbf) @ 3400 rpmapplicationsVW Eurovan, VW Sharan, VW Golf VR6, VW Jetta[edit]220 hp 3.0 V6Audi 3.0 V6 engine cutawayThis engine unveiled in 2000 is an aluminium, longer stroke version of the 2.8L V6.Engine codeA VKconfiguration2976 cc 90°V6headfive-valve cylinder, continuous intake camshaft adjustment, exhaust camshaft adjustmentoutput162 kW (220 hp) at 6300 rpm, 300 N·m at 3200 rpmblockaluminium, bore 81 mm × stroke 96,3 mm, light pistons, balancer shaftaspirationtwo-position variable intake manifoldmanagementBosch Motronic ME 7.1.1 with electronic throttle controlekhaustEU4 compliantapplication2000 Audi A4referencesAudi AG (2000-10-10). The New Audi A4. Press release.[edit]250 hp 3.2L VR63.2 VR6 engineConfiguration3189 cm3 15°VR6Cylindersbore * stroke 84*95.9 mm, 531 cc per cylinderHeadfour-valve, two overhead camshafts per cylinder bank, continuous timing adjustment, 52 degrees on the inlet, 22 degrees on the outlet, roller rocker arms with hydraulic play compensationIgnitionindividual ignition coilOutput173 kW (235 hp) @ 6,200 rpm, 315 N·m from 2950 rpm in T5176 kW (241 hp) @ 6,200 rpm, 320 N·m from 2,500 to 3,000 rpm184 kW (250 hp) @ 6,300 rpm, 320 N·m from 2,500 to 3,000 rpmSourcesGermanCarFans New Volkswagen Golf R32 09-23-2005applicationsVW Golf R32, Audi A3, Audi TT, VW Touareg, Audi Q7, Porsche Cayenne, VW Phaeton[edit]255/260 hp 3.2L V6 FSI3.2L V6 FSI cutawayEngine codeBKHConfiguration3123 cm3 90° V6CylindersBore × stroke 84.5 mm × 92.8 mm (0.91 ratio), 520.4 cc/cylinder, 90 mm spaced, aluminium blockCrankshaftaluminiumHeadsaluminium, 4 valves per cylinder, DOHC, 12.5:1 Compression ratio, chain driven camshafts, continuously variable valve timing system both for intake and exhaustFuel systemcommon rail FSI high-pressure injection between 30 and 100 bar.Aspirationvariable intake manifoldExhausttwo ceramic catalytic convertersDimensions360 mm length, 430 mm width, 169.5 kg (aluminium engine)Output188 kW (255 hp) @ 6500 rpm, 330 N·m @ 3250 rpm, 90% available between 1900 and 5900 rpm, 7200 rpm max191 kW (260 hp) @ 6500 rpm in the A8.Applications2005 Audi A8, Audi A6, Audi A4referencesAudi AG (2004-04-08). New Audi A6 In Depth. Press release.[edit]280 hp 3.6L VR6 FSIThis bigger VR6 with a narrower angle will be made available for the US market before Europe.Configuration3598 cc 10.6° VR6CylindersBore x stroke: 89.0 x 96.4 mm, iron blockHeadaluminum, chain-driven double overhead cams, 4 valves per cylinder, hydraulic lifters, variable intake- and exhaust-valve timing, 12.0:1 compression ratioFuel systemFSI direct injectionOutput206 kW (280 hp DIN) @ 6200 rpm, 360 N·m (266 ft·lbf) @ 2750 rpm, 12,57 bars MEP, max 6500 rpm (20.9 m/s piston speed)ApplicationsUS 2006 VW Passat, future US VW Golf R36, 2006 Audi Q7referencesV olkswagen Passat 3.6. Car and Driver (December 2005).[edit]Eight cylinder[edit]280 hp 3.7 V8Configuration3,697 cm³V8-90°, bore × stroke 84,5 × 82,4 mmHead40 valves actuated by low friction roller fingers 11.0:1 Compression ratioAspiration3-stage variable composite intake manifoldaluminium, five bearingsManagementBosch MotronicOutput206 kW (280 hp) @ 6,000 rpm, 360 N·m @ 3,750 rpmFuelRegular Premium unleaded recommended for maximum performance.ApplicationsAudi A8[edit]275 hp 4.0L W8Volksagen 4.0L W8 engine cutaway photoConfiguration3,998 cm³ (4.0 L) WR8, two 15° "VR4" engines mated at 72°Head32 valves actuated by roller rocker fingers, 52° variable inlet camshafts and 22° for exhaust camshafts, 10.8:1 CompressionratioAspirationaluminium resonance intake manifoldCrankcasealuminium, five bearings, counter-rotating at twice the crankshaft speed Lancaster principle balancer shafts one above the other, symmetric to the middle of the crankshaft, upper one driven by a toothed beltManagementBosch MotronicDimensions190 kg, 420 mm length, 710 mm width, 683 mm heightOutput202 kW (275 hp DIN) @ 6,000 rpm, 370 N·m (11.6 bars MEP) @ 2,750 rpm, max speed 6400 rpm (19.2 m/s)FuelRegular Premium unleaded recommended for maximum performance.VW Passat and Passat WagonreferencesVW AG (2002-04-22). VW Passat W8 4Motion. Press release.[edit]335/340 hp 4.2L V84.2L V8 cutawayEngine codeBHFConfiguration4163 cm3 90°V8CylindersBore × stroke 84.5 mm × 92.8 mm (0.91 ratio), 520.4 cc/cylinder, 90 mm spaced, aluminium block CrankcasealuminiumHeadsaluminium, 4 valves per cylinder, DOHC, chain driven camshaftsAspirationsynthetic material two-stage variable intake manifoldExhausttwo multi-stage catalytic convertersEngine managementBosch Motronic ME 7.1.1.Dimensions464 mm length, 195 kgOutput246 kW (335 hp) @ 6600 rpm, 420 N·m @ 3500 rpm, 6800 rpm max250 kW (340 hp) @ 7,000 rpm in the S4Applicationsfirst in Audi S4 in 2002, Audi A6, Audi A8referencesAudi AG (2004-04-08). New Audi A6 In Depth. Press release.[edit]350-420 hp 4.2 V8 FSIAudi 4.2 V8 FSI engine cutawayconfiguration4163 cm³ 90° V8cylinders90 mm spacing, aluminium-silicon alloy housing, hard silicon crystals linersheadfour chains driven camshaftsaspirationmagnesium two-stage variable intake manifoldfuelFSI direct petrol injectionmanagementMotronic MED 9.1output257 kW (350 hp) at 6800 rpm, 440 N·m at 3,500 rpm, 85% available from 2000 rpm in the 2006 Audi Q7 and 2007 VW Touareg265 kW (360 hp) at 6900 rpm, 440 N·m at 3,500 rpm in the 2007 Audi A6 and Audi A8309 kW (420 hp) @ 7800 rpm, 430 N·m @ 5500 rpm, 90% available between 2,250 and 7,600 rpm, 8,250 rpm maximum in the 2005 Audi RS4 and Audi R8 (road car)referencesAudi AG (2005-09-05). New Audi RS4. Press release.Audi AG (2006-01-31). Audi Q7 In Depth. Press release.[edit]RS6 450 hp 4.2L V8 biturboAspirationtwo fast-acting turbochargers (one per bank), two intercoolers optimised to prevent pressure lossHeadfive valves per cylinder (three inlet and two exhaust), roller-bearing rocker armsOutput331 kW (450 bhp) between 5700 and 6400 rpm, 560 N·m between 1950 and 5600 rpmApplications2004 Audi RS6referencesAudi AG. Audi RS6 in depth. Press release.[edit]Ten cylinder[edit]420-450 hp 5.2L V10 FSIThis engine is a derivative of the Gallardo's Lamborghini V10 developed under the VAG era. It has been bored by an extra two millimeters, and shares the 90° angle of the recent Audi V engines. Audi continue to use the FSI technology in the Le Mans R8 sport cars. A 550 hp 5.5L version will be used in the upcomming Audi Q7 and the Audi RS6. A 600 hp bi-turbo V10 will power the Audi R8 Road Car according to WorldCarFansAudi 5.2L V10 engine and gearbox cutaway photoAudi 5.2L V10 engine cutaway drawingConfiguration5204 cm3 90°V10CylindersBore × stroke 84.5 mm × 92.8 mm (0.91 ratio), 520.4 cc/cylinder, 90 mm spaced, 18.5 mm bank offsetCrankcaselow-pressure die-casting hypereutectic aluminium alloy reinforced by a bedplate frame, inner-vee balancing shafteliminating first degree inertial forces, grey cast iron bearingsCrankshaft18 degrees crankpin offsetHead4 valves per cylinder, DOHC, 12.5:1 Compression ratio, chain driven camshafts continuously adjusted on 42 degrees, rollercam followers valve actuation, 32.5 mm intake valves and 28.0 mm exhaust sodium-filled valvesFuel systemcommon rail FSI petrol direct injection, maximum injection pressure of 100 bar, Bosch Motronic MED 9.1 management Aspirationtwo-stage magnesium variable intake manifold incorporating electronically controlled tumble flaps inducing a swirling movement in the drawn airExhaustfour close-coupled catalytic convertersDimensions220 kg (20 kg less than the competition, i.e. the BMW S85), length 685 mm, width 801 mm, height 713 mm high with all components, the engine only is 560 mm longOutput320 kW (435 hp) @ 6800 rpm, 540 N·m from 3000 to 4000 rpm, over 500 N·m between 2500 and 5500 rpm in the S6 and S6 Avant331 kW (450 hp) @ 7000 rpm, 540 N·m @ 3500 rpm (90% available from 2,300 rpm), 21.7 m/s maximum piston speed, 13,04 bars maximum MEP in the S8ApplicationsAudi S8, Audi S6 and S6 AvantreferencesAudi AG (2005-10-19). New Audi S8. Press release.Audi AG (2005-12-02). New Audi S8 In Depth. Press release.[edit]Twelve cylinder[edit]420/450 hp 6.0L W12The W12 is 12 cylinder W engine formed by two 15° VR6 engines placed on a single crankshaft at a 72° an gle. It is also used with slight modification and the addition of turbochargers in the Bentley Continental GT and Bentley Continental Flying Spur. It has been used in a 600 hp form aboard the Volkswagen W12prototype sports car to establish a 24 hour record of 323 km/h in 2002 at Nardo, Italia.W12 cutawayConfiguration5,998 cc water cooled W12CylindersBore × stroke 84.00 × 90.20 mm (0.93 ratio), 500 cc /cylinder, 10.7:1 compression ratioBlockaluminium alloy, torsionally stiff aluminium crankcase with high-resistance cylinder linersCrankshaft21.2 kg, seven bearings, crankpins offset to achieve a constant firing order as on a V6 engineHeadaluminium, twin constantly variable camshaft, 52 degrees timing range for the flow-optimised inlet ports, 22 degrees on the exhaust camshaftsFuel systemsingle coils centrally positioned spark plugs, electronic fuel injetionAspirationtwo-channel magnesium intake manifoldExhaustfour pre-catalysts and two main catalytic converters then four close-coupled ceramic catalytic converters, eight heated oxygen sensors monitoringEngine managementBosch Motronic ME 7.1.1, electronic sequential injection, electronic throttle control, hot-film air-mass sensing, cylinder-selective knock control via four sensors and permanent lambda controlDimensions513 mm length, 715 mm height, 710 then 690 mm widthOutput309 kW (420 hp) and 550 N·m, then 331 kW (450 hp) @ 6,200 rpm, 580Nm @ 4,000 rpm, 560 N·m from 2,300 to 5,300 rpmApplications2004 Audi A8, 2004 VW Phaeton, 2004 VW Touareg sportreferencesVW AG (02-25-2004). VW Phaeton - In Depth. Press release.Audi AG (01-12-2004). 12-cylinder Audi A8 L Details. Press release.[edit]Sixteen cylinder。

Lassen iQ GPS模块说明书

Lassen iQ GPS模块说明书

Key Featuresand Benefits• Ultra-low power: 86 mW• Trimble quality at low cost• Aided GPS through TSIP for faster acquisition• Dual sensitivity modes with automatic switching• 12-channel simultaneous operation • Supports NMEA 0183, TSIP, TAIP and DGPS Lassen iQ GPS ModuleLow-power, high-quality GPS solution for your mobile productsT rimble’s Lassen® iQ module isone smart buy. It adds powerful,12-channel GPS functionalityto your mobile product in apostage-stamp-sized footprintwith ultra-low power consump-tion and extreme reliability—allat a very economical price.Designed for portable handheld,battery-powered applicationssuch as cell phones, pagers,PDAs, digital cameras, and manyothers, the module is also idealfor standard GPS applicationssuch as tracking.The 12-channel Lassen iQmodule is fully compatible withT rimble’s popular Lassen SQmodule. Using T rimble’s break-through, patented FirstGPS®architecture, the module deliverscomplete position, velocity andtime (PVT) solutions for use inthe host application.Powerful PerformanceThe Lassen iQ module fea-tures two GPS signal sensitivitymodes: Standard and Enhanced.With Enhanced mode enabled,the module automaticallyswitches to higher sensitivitywhen satellite signals are weak.The module also supports TSIPdownload of critical startupinformation for fast acquisition.This aided GPS (A-GPS) startupprovides hot start performancefor each power-up.The Lassen iQ module is the onlystamp-sized GPS product thatsupports the four most popu-lar protocols: DGPS (RTCM),TSIP(T rimble Standard InterfaceProtocol), TAIP (T rimble ASCIIInterface Protocol) and NMEA 0183.The Lassen iQ module combinesT rimble performance and qual-ity with low cost. With an MTBF(mean time between failures) fi gureof 60 years, it is one of the most reli-able GPS receivers on the market.HardwareA metal shield encloses themodule for protection and easeof handling. The package hasa small form factor, (approxi-mately 26 mm x 26 mm,including the shield). It typi-cally requires less than 90 mWof power at 3.3 VDC.The highly integrated moduleis a miniature board containingT rimble GPS hardware corebased on our Colossus® RFASIC and IO-TS digital signalprocessor (DSP), a 32-bit RISCCPU and fl ash memory.AntennasThe Lassen iQ module is com-patible with active, 3.3-VDCantennas. Three such antennasare available from T rimble andare recommended for use accord-ing to your application; see thereverse side for antenna details.The module provides both anten-na open and short detection plusantenna short protection.Starter KitThe Lassen iQ Starter Kit pro-vides everything you need toget started integrating state-of-the-art GPS capability into yourapplication.Lassen iQ GPS receiver with metal shieldLassen iQ GPS ModuleLow-power, high-quality GPS solution for your mobile productsVibration0.008 g 2/Hz 5 Hz to 20 Hz 0.05 g 2/Hz 20 Hz to 100 Hz–3 dB/octave 100 Hz to 900 HzOperating Humidity5% to 95% R.H. non-condensing, at +60° CEnclosureMetal enclosure with solder mounting tabs Dimensions26 mm W x 26 mm L x 6 mm H(1.02” W x 1.02” L x 0.24” H)Weight6.5 grams (0.2 ounce) including shieldnGothDEMI 7ptModuleLassen iQ module, in metal enclosure with soldermounting tabs Starter Kit Includes Lassen iQ module mounted on interface motherboard in a durable metal enclosure, AC/DC power converter, compact magnetic-mount GPS antenna, ultra-compact embedded antenna, serial interface cable, cigarette lighter adapter, TSIP , NMEA, and TAIP protocols, software toolkit and manual on CD-ROMAntenna Transition Cable, MCXRF cable for connecting antennas with MCX connector to on-module H.FL-RF connector. Cable length: 10 cmAntenna Transition Cable, SMARF cable for connecting antennas with SMA connector to on-module H.FL-RF connector.Cable length: 12.9 cm.Ultra-Compact Embedded Antenna3.3V active miniature unpackaged antennaCable length: 8 cmDim: 22 mm W x 21 mm L x 8 mm H (0.866” x 0.827” x 0.315”)Connector: HFL; mates directly to on-module RF connectorCompact Unpackaged Antenna3V active micropatch unpackaged antenna Cable length: 11 cmDim: 34.6 mm W x 29 mm L x 9 mm H (1.362” x 1.141” x 0.354”)Connector: MCX; mates through the optional RF transition cable to on-module RF connectorCompact Magnetic-Mount Antenna, MCX or SMA3V active micropatch antenna with magnetic mount Cable length: 5 mDim: 42 mm W x 50.5 mm L x 13.8 mm H (1.65” x 1.99” x 0.55”)Connectors: MCX or SMA, mates through the optional RF trasition cable to the module RF connectorSpecifi cations subject to change without notice.© C o p y r i g h t 2004, T r i m b l e N a v i g a t i o n L i m i t e d . A l l r i g h t s r e s e r v e d . T h e G l o b e a n d T r i a n g l e , T r i m b l e , C o l o s s u s , F i r s t G P S , a n d L a s s e n a r e t r a d e m a r k s o f T r i m b l e N a v i g a t i o n L i m i t e d r e g i s t e r e d i n t h e U n i t e d S t a t e s P a t e n t a n d T r a d e m a r k O f fi c e . A l l o t h e r t r a d e m a r k s a r e t h e p r o p e r t y o f t h e i r r e s p e c t i v e o w n e r s . T I D 13442 (9/04)• 12-channel simultaneous operation• Ultra-low power consumption: less than 90 mW (27 mA) @ 3.3 V • Dual sensitivity modes with automatic switching • Aided GPS through TSIP• Antenna open and short circuit detection and protection • Compact size: 26 mm W x 26 mm L x 6 mm H• Supports NMEA 0183, TSIP , TAIP , DGPS protocols • Trimble quality at low costGeneralL1 (1575.42 MHz) frequency, C/A code, 12-channel,continuous tracking receiverUpdate Rate TSIP @ 1 Hz; NMEA @ 1 HZ; TAIP @ 1 Hz Accuracy Horizontal: <5 meters (50%), <8 meters (90%) Altitude: <10 meters (50%), <16 meters (90%) Velocity: 0.06 m/sec PPS (static): ±50 nanosecondsAcquisition (Autonomous Operation in Standard Sensitivity Mode) Reacquisition: <2 sec. (90%) Hot Start: <10 sec (50%), <13 sec (90%) Warm Start: <38 sec (50%), <42 sec (90%) Cold Start: <50 sec (50%), <84 sec (90%)Cold start requires no initialization. Warm start implies last position, time and almanac are saved by backup power. Hot start implies ephemeris also saved.Operational (COCOM) LimitsAltitude: 18,000 mVelocity: 515 m/sEither limit may be exceeded, but not bothConnectorsI/O:8-pin (2x4) 2 mm male header, micro terminal strip ASP 69533-01 RF: Low-profi le coaxial connectorH.FL-R-SMT (10), 50 Ohm Serial Port 2 serial ports (transmit/receive)PPS3.3 V CMOS-compatible TTL-level pulse, once per secondProtocolsTSIP , TAIP , NMEA 0183 v3.0, RTCM SC-104 NMEA MessagesGGA, VTG, GLL, ZDA, GSA, GSV and RMC Messages selectable by TSIP commandSelection stored in fl ash memory- BFranGothDEMI 7ptPrime Power+3.0 VDC to 3.6 VDC (3.3 V typ.) Power ConsumptionLess than 90 mW (27 mA) @ 3.3 VBackup Power +2.5 VDC to +3.6 VDC (3.0V typ.)Ripple Noise Max 60 mV, peak to peak from 1 Hz to 1 MHz Antenna Fault Protection Open and short circuit detection and protectionOperating Temperature –40° C to +85° C Storage Temperature–55° C to +105° CT rimble Navigation Limited is not responsible for the operation or failure of operation ofGPS satellites or the availability of GPS satellite signals.Trimble Navigation Limited Corporate Headquarters 645 North Mary Avenue Sunnyvale, CA Trimble Navigation Europe Ltd, UKPhone: 44 1256-760-150Trimble Export Ltd, Korea Phone: 82-2-5555-361***********************Trimble Navigation Ltd, ChinaPhone: 86-21-6391-7814/iQ。

CellTiter Glo Luminescent Cell Viability Assay Protocol

CellTiter Glo Luminescent Cell Viability Assay Protocol

Promega Corporation ·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·1.Description (1)2.Product Components and Storage Conditions (4)3.Performing the CellTiter-Glo ®Assay (5)A.Reagent Preparation (5)B.Protocol for the Cell Viability Assay (6)C.Protocol for Generating an ATP Standard Curve (optional) (7)4.Appendix (7)A.Overview of the CellTiter-Glo ®Assay..............................................................7B.Additional Considerations..................................................................................8C.References............................................................................................................11D.Related Products. (12)1.DescriptionThe CellTiter-Glo ®Luminescent Cell Viability Assay (a–e)is a homogeneous method to determine the number of viable cells in culture based on quantitation of the ATP present, which signals the presence of metabolically active cells. The CellTiter-Glo ®Assay is designed for use with multiwell-plate formats, making it ideal for automated high-throughput screening (HTS) and cell proliferation and cytotoxicity assays. The homogeneous assay procedure (Figure 1) involves adding a single reagent (CellTiter-Glo ®Reagent) directly to cells cultured in serum-supplemented medium. Cell washing, removal of medium or multiple pipetting steps are not required.The homogeneous “add-mix-measure” format results in cell lysis and generation of a luminescent signal proportional to the amount of ATP present (Figure 2).The amount of ATP is directly proportional to the number of cells present in culture in agreement with previous reports (1). The CellTiter-Glo ®Assay relies on the properties of a proprietary thermostable luciferase (Ultra-Glo™ Recombinant Luciferase), which generates a stable “glow-type” luminescent signal and improves performance across a wide range of assay conditions. The luciferase reaction for this assay is shown in Figure 3. The half-life of the luminescent signal resulting from this reaction is greater than five hours (Figure 4). This extended half-life eliminates the need for reagent injectors and provides flexibility for continuous or batch-mode processing of multiple plates. The unique homogeneous format reduces pipetting errors that may be introduced during the multiple steps required by other ATP-measurement methods.CellTiter-Glo ®Luminescent Cell Viability AssayAll technical literature is available on the Internet at: /protocols/ Please visit the web site to verify that you are using the most current version of this Technical Bulletin. Please contact Promega Technical Services if you have questions on useofthissystem.E-mail:********************Figure 1. Flow diagram showing preparation and use of CellTiter-Glo ®Reagent.Promega Corporation ·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·3170M A 12_0ACellTiter-Glo CellTiter-Glo MixerLuminometer®System Advantages•Homogeneous:“Add-mix-measure” format reduces the number of plate-handling steps to fewer than that required for similar ATP assays.•Fast:Data can be recorded 10 minutes after adding reagent.•Sensitive:Measures cells at numbers below the detection limits of standard colorimetric and fluorometric assays.•Flexible:Can be used with various multiwell formats. Data can be recorded by luminometer or CCD camera or imaging device.•Robust:Luminescent signal is very stable, with a half-life >5 hours,depending on cell type and culture medium used.•Able to Multiplex:Can be used with reporter gene assays or other cell-based assays from Promega (2,3).Figure 3. The luciferase reaction.Mono-oxygenation of luciferin is catalyzed byluciferase in the presence of Mg 2+, ATP and molecular oxygen.Promega Corporation ·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·3171M A 12_0A L u m i n e s c e n c e (R L U )Cells per Well10,00060,00020,00030,00040,00050,0000R² = 0.9990.5 × 1061.0 × 1061.5 × 1062.0 × 1062.5 × 1063.0 × 1063.5 × 1064.0 × 106r² = 0.99020,00010,00030,00040,00050,000r² = 0.9900100200300400HO SN S N O S N S N OCOOH +ATP+O 2Ultra-Glo™ Recombinant Luciferase +AMP+PP i +CO 2+LightBeetle Luciferin OxyluciferinMg 2+0Figure 2. Cell number correlates with luminescent output.A direct relationship exists between luminescence measured with the CellTiter-Glo ®Assay and the number of cells in culture over three orders of magnitude. Serial twofold dilutions of HEK293cells were made in a 96-well plate in DMEM with 10% FBS, and assays wereperformed as described in Section 3.B. Luminescence was recorded 10minutes after reagent addition using a GloMax ®-Multi+ Detection System. Values represent the mean ± S.D. of four replicates for each cell number. The luminescent signal from 50HEK293 cells is greater than three times the background signal from serum-supplemented medium without cells. There is a linear relationship (r 2= 0.99)between the luminescent signal and the number of cells from 0to 50,000 cells per well.Figure 4. Extended luminescent half-life allows high-throughput batchprocessing.Signal stability is shown for three common cell lines. HepG2 and BHK-21cells were grown and assayed in MEM containing 10% FBS, while CHO-K1 cells were grown and assayed in DME/F-12 containing 10% FBS. CHO-K1, BHK-21 and HepG2 cells, at 25,000 cells per well, were added to a 96-well plate. After an equal volume of CellTiter-Glo ®Reagent was added, plates were shaken and luminescence monitored over time with the plates held at 22°C. The half-lives of the luminescent signals for the CHO-K1, BHK-21 and HepG2 cells were approximately 5.4, 5.2 and5.8hours, respectively.2.Product Components and Storage ConditionsProduct Size Cat.#CellTiter-Glo ®Luminescent Cell Viability Assay 10ml G7570Substrate is sufficient for 100 assays at 100µl/assay in 96-well plates or 400 assays at 25µl/assay in 384-well plates. Includes:• 1 × 10mlCellTiter-Glo ®Buffer • 1 vial CellTiter-Glo ®Substrate (lyophilized)Product Size Cat.#CellTiter-Glo ®Luminescent Cell Viability Assay 10 × 10ml G7571Each vial of substrate is sufficient for 100 assays at 100µl/assay in 96-well plates or 400 assays at 25µl/assay in 384-well plates (1,000 to 4,000 total assays). Includes:•10 × 10mlCellTiter-Glo ®Buffer •10 vials CellTiter-Glo ®Substrate (lyophilized)Promega Corporation ·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·R e l a t i v e L u m i n e s c e n c e (%)Time (minutes)CHO-K101020304050607080901003173M A 12_0AProduct Size Cat.# CellTiter-Glo®Luminescent Cell Viability Assay100ml G7572 Substrate is sufficient for 1,000 assays at 100µl/assay in 96-well plates or 4,000assays at 25µl/assay in 384-well plates. Includes:•1 × 100ml CellTiter-Glo®Buffer• 1 vial CellTiter-Glo®Substrate (lyophilized)Product Size Cat.# CellTiter-Glo®Luminescent Cell Viability Assay10 × 100ml G7573Each vial of substrate is sufficient for 1,000 assays at 100µl/assay in 96-well plates or4,000 assays at 25µl/assay in 384-well plates (10,000to 40,000 total assays). Includes:•10 × 100ml CellTiter-Glo®Buffer•10 vials CellTiter-Glo®Substrate (lyophilized)Storage Conditions:For long-term storage, store the lyophilized CellTiter-Glo®Substrate and CellTiter-Glo®Buffer at –20°C. For frequent use, the CellTiter-Glo®Buffer can be stored at 4°C or room temperature for 48hours without loss of activity. See product label for expiration date information. ReconstitutedCellTiter-Glo®Reagent (Buffer plus Substrate) can be stored at room temperaturefor up to 8hours with <10% loss of activity, at 4°C for 48hours with ~5% lossof activity, at 4°C for 4days with ~20% loss of activity or at –20°C for 21weekswith ~3% loss of activity. The reagent is stable for up to ten freeze-thaw cycles,with less than 10% loss of activity.3.Performing the CellTiter-Glo®AssayMaterials to Be Supplied by the User•opaque-walled multiwell plates adequate for cell culture•multichannel pipette or automated pipetting station for reagent delivery•device (plate shaker) for mixing multiwell plates•luminometer, CCD camera or imaging device capable of reading multiwell plates •optional:ATP for use in generating a standard curve (Section 3.C)3.A.Reagent Preparation1.Thaw the CellTiter-Glo®Buffer, and equilibrate to room temperature priorto use. For convenience the CellTiter-Glo®Buffer may be thawed andstored at room temperature for up to 48hours prior to use.2.Equilibrate the lyophilized CellTiter-Glo®Substrate to room temperatureprior to use.Promega Corporation·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·3.A.Reagent Preparation (continued)3.Transfer the appropriate volume (10ml for Cat.# G7570 and G7571, or 100mlfor Cat.# G7572 and G7573) of CellTiter-Glo ®Buffer into the amber bottlecontaining CellTiter-Glo ®Substrate to reconstitute the lyophilizedenzyme/substrate mixture. This forms the CellTiter-Glo ®Reagent.4.Mix by gently vortexing, swirling or inverting the contents to obtain ahomogeneous solution. The CellTiter-Glo ®Substrate should go intosolution easily in less than 1minute.3.B.Protocol for the Cell Viability AssayWe recommend that you perform a titration of your particular cells todetermine the optimal number and ensure that you are working within thelinear range of the CellTiter-Glo ®Assay. Figure 2 provides an example of sucha titration of HEK293 cells using 0 to 50,000 cells per well in a 96-well format.1.Prepare opaque-walled multiwell plates with mammalian cells in culturemedium, 100µl per well for 96-well plates or 25µl per well for 384-wellplates.Multiwell plates must be compatible with the luminometer used.2.Prepare control wells containing medium without cells to obtain a value forbackground luminescence.3.Add the test compound to experimental wells, and incubate according toculture protocol.4.Equilibrate the plate and its contents at room temperature forapproximately 30 minutes.5.Add a volume of CellTiter-Glo ®Reagent equal to the volume of cell culturemedium present in each well (e.g., add 100µl of reagent to 100µl of mediumcontaining cells for a 96-well plate, or add 25µl of reagent to 25µl ofmedium containing cells for a 384-well plate).6.Mix contents for 2 minutes on an orbital shaker to induce cell lysis.7.Allow the plate to incubate at room temperature for 10 minutes to stabilizeluminescent signal.Note:Uneven luminescent signal within standard plates can be caused bytemperature gradients, uneven seeding of cells or edge effects in multiwellplates.8.Record luminescence.Note:Instrument settings depend on the manufacturer. An integration timeof 0.25–1 second per well should serve as a guideline.Promega Corporation ·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·3.C.Protocol for Generating an ATP Standard Curve (optional)It is a good practice to generate a standard curve using the same plate onwhich samples are assayed. We recommend ATP disodium salt (Cat.# P1132,Sigma Cat.# A7699 or GE Healthcare Cat.# 27-1006). The ATP standard curveshould be generated immediately prior to adding the CellTiter-Glo®Reagentbecause endogenous ATPase enzymes found in sera may reduce ATP levels.1.Prepare 1µM ATP in culture medium (100µl of 1µM ATP solution contains10–10moles ATP).2.Prepare serial tenfold dilutions of ATP in culture medium (1µM to 10nM;100µl contains 10–10to 10–12moles of ATP).3.Prepare a multiwell plate with varying concentrations of ATP standard in100µl medium (25µl for a 384-well plate).4.Add a volume of CellTiter-Glo®Reagent equal to the volume of ATPstandard present in each well.5.Mix contents for 2 minutes on an orbital shaker.6.Allow the plate to incubate at room temperature for 10 minutes to stabilizethe luminescent signal.7.Record luminescence.4.Appendix4.A.Overview of the CellTiter-Glo®AssayThe assay system uses the properties of a proprietary thermostable luciferase toenable reaction conditions that generate a stable “glow-type” luminescentsignal while simultaneously inhibiting endogenous enzymes released duringcell lysis (e.g., ATPases). Release of ATPases will interfere with accurate ATPmeasurement. Historically, firefly luciferase purified from Photinus pyralis(LucPpy) has been used in reagents for ATP assays (1,4–7). However, it hasonly moderate stability in vitro and is sensitive to its chemical environment,including factors such as pH and detergents, limiting its usefulness fordeveloping a robust homogeneous ATP assay. Promega has successfullydeveloped a stable form of luciferase based on the gene from another firefly,Photuris pennsylvanica(LucPpe2), using an approach to select characteristics thatimprove performance in ATP assays. The unique characteristics of this mutant(LucPpe2m) enabled design of a homogeneous single-reagent-addition approachto perform ATP assays with cultured cells. Properties of the CellTiter-Glo®Reagent overcome the problems caused by factors, such as ATPases, thatinterfere with ATP measurement in cell extracts. The reagent is physicallyrobust and provides a sensitive and stable luminescent output.Promega Corporation·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·4.A.Overview of the CellTiter-Glo®Assay (continued)Sensitivity and Linearity:The ATP-based detection of cells is more sensitivethan other methods (8–10). In experiments performed by Promega scientists,the luminescent signal from 50HEK293 cells is greater than three standarddeviations above the background signal from serum-supplemented mediumwithout cells. There is a linear relationship (r2= 0.99) between the luminescentsignal and the number of cells from 0 to 50,000 cells per well in the 96-wellformat. The luminescence values in Figure 2 were recorded after 10minutes ofincubation at room temperature to stabilize the luminescent signal as describedin Section3.B. Incubation of the same 96-well plate used in the experimentshown in Figure 2 for 360minutes at room temperature had little effect on therelationship between luminescent signal and number of cells (r2= 0.99).Speed:The homogeneous procedure to measure ATP using the CellTiter-Glo®Assay is quicker than other ATP assay methods that require multiple steps toextract ATP and measure luminescence. The CellTiter-Glo®Assay also is fasterthan other commonly used methods to measure the number of viable cells(such as MTT, alamarBlue®or Calcein-AM) that require prolonged incubationsteps to enable the cells’ metabolic machinery to convert indicator moleculesinto a detectable signal.4.B.Additional ConsiderationsTemperature:The intensity and decay rate of the luminescent signal from theCellTiter-Glo®Assay depends on the luciferase reaction rate. Environmentalfactors that affect the luciferase reaction rate will change the intensity andstability of the luminescent signal. Temperature is one factor that affects therate of this enzymatic assay and thus the light output. For consistent results,equilibrate assay plates to a constant temperature before performing the assay.Transferring eukaryotic cells from 37°C to room temperature has little effect onATP content (5). We have demonstrated that removing cultured cells from a37°C incubator and allowing them to equilibrate to 22°C for 1–2 hours hadlittle effect on ATP content. For batch-mode processing of multiple assayplates, take precautions to ensure complete temperature equilibration. Platesremoved from a 37°C incubator and placed in tall stacks at room temperaturewill require longer equilibration than plates arranged in a single layer.Insufficient equilibration may result in a temperature gradient effect betweenwells in the center and at the edge of the plates. The temperature gradientpattern also may depend on the position of the plate in the stack.Promega Corporation·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·Chemicals:The chemical environment of the luciferase reaction affects theenzymatic rate and thus luminescence intensity. Differences in luminescenceintensity have been observed using different types of culture media and sera.The presence of phenol red in culture medium should have little impact onluminescence output. Assaying 0.1µM ATP in RPMI medium without phenolred resulted in ~5% increase in luminescence output (in relative light units[RLU]) compared to assays in RPMI containing the standard concentration ofphenol red, whereas assays in RPMI medium containing twice the normalconcentration of phenol red showed a ~2% decrease in luminescence.Solvents for the various test compounds may interfere with the luciferasereaction and thus the light output from the assay. Interference with theluciferase reaction can be detected by assaying a parallel set of control wellscontaining medium without cells. Dimethylsulfoxide (DMSO), commonly usedas a vehicle to solubilize organic chemicals, has been tested at finalconcentrations of up to 2% in the assay and only minimally affects light output.Plate Recommendations:We recommend using standard opaque-walledmultiwell plates suitable for luminescence measurements. Opaque-walledplates with clear bottoms to allow microscopic visualization of cells also maybe used; however, these plates will have diminished signal intensity andgreater cross talk between wells. Opaque white tape may be used to decreaseluminescence loss and cross talk.Cellular ATP Content:Different cell types have different amounts of ATP,and values reported for the ATP level in cells vary considerably (1,4,11–13).Factors that affect the ATP content of cells may affect the relationship betweencell number and luminescence. Anchorage-dependent cells that undergocontact inhibition at high densities may show a change in ATP content per cellat high densities, resulting in a nonlinear relationship between cell numberand luminescence. Factors that affect the cytoplasmic volume or physiology ofcells also will affect ATP content. For example, oxygen depletion is one factorknown to cause a rapid decrease in ATP (1).Promega Corporation·2800 Woods Hollow Road ·Madison, WI 53711-5399 USA Toll F ree in USA 800-356-9526·Phone 608-274-4330 ·F ax 608-277-2516 ·4.B.Additional Considerations (continued)Mixing:Optimal assay performance is achieved when the CellTiter-Glo®Reagent is mixed completely with the cultured cells. Suspension cell lines (e.g., Jurkat cells) generally require less mixing to achieve lysis and extract ATP than adherent cells (e.g., L929 cells). Tests were done to evaluate the effect ofshaking the plate after adding the CellTiter-Glo® Reagent. Suspension cellscultured in multiwell plates showed only minor differences in light outputwhether or not the plates were shaken after adding the CellTiter-Glo®Reagent.Adherent cells are more difficult to lyse and show a substantial differencebetween shaken and nonshaken plates.Several additional parameters related to reagent mixing include the force ofdelivery of CellTiter-Glo®Reagent, sample volume and dimensions of the well.All of these factors may affect assay performance. The degree of reagent mixing required may be affected by the method used to add the CellTiter-Glo®Reagent to the assay plates. Automated pipetting devices using a greater or lesser force of fluid delivery may affect the degree of subsequent mixing required.Complete reagent mixing in 96-well plates should be achieved using orbitalplate shaking devices built into many luminometers and the recommended2-minute shaking time. Special electromagnetic shaking devices that use aradius smaller than the well diameter may be required to efficiently mixcontents of 384-well plates. The depth of medium and geometry of themultiwell plates may have an effect on mixing efficiency. We recommend that you take these factors into consideration when performing the assay andempirically determine whether a mixing step is necessary for the individualapplication.LuminometersFor highly sensitive luminometric assays, the luminometer model and settings greatly affect the quality of data obtained. Luminometers from differentmanufacturers will vary in sensitivities and dynamic ranges. We recommend the GloMax®products because these instruments do not require gainadjustments to achieve optimal sensitivity and dynamic range. Additionally, GloMax®instruments are preloaded with Promega protocols for ease of use.If you are not using a GloMax®luminometer, consult the operating manual for your luminometer to determine the optimal settings. The limits should beverified on each instrument before analysis of experimental samples. The assay should be linear in some portion of the detection range of the instrument used.For an individual luminometer there may be different gain settings. Werecommend that you optimize the gain settings.4.C.References1.Crouch, S.P. et al.(1993) The use of ATP bioluminescence as a measure of cellproliferation and cytotoxicity. J. Immunol. Methods160, 81–8.2.Farfan, A.et al.(2004) Multiplexing homogeneous cell-based assays. Cell Notes10, 2–5.3.Riss, T., Moravec, R. and Niles, A. (2005) Selecting cell-based assays for drugdiscovery screening. Cell Notes13, 16–21.4.Kangas, L., Grönroos, M. and Nieminen, A.L. (1984) Bioluminescence of cellular ATP:A new method for evaluating cytotoxic agents in vitro. Med. Biol.62, 338–43.5.Lundin, A. et al.(1986) Estimation of biomass in growing cell lines by adenosinetriphosphate assay.Methods Enzymol. 133, 27–42.6.Sevin, B.U. et al.(1988) Application of an ATP-bioluminescence assay in human tumorchemosensitivity testing. Gynecol. Oncol.31, 191–204.7.Gerhardt, R.T.et al.(1991) Characterization of in vitro chemosensitivity ofperioperative human ovarian malignancies by adenosine triphosphatechemosensitivity assay. Am. J. Obstet. Gynecol. 165, 245–55.8.Petty, R.D. et al.(1995) Comparison of MTT and ATP-based assays for themeasurement of viable cell number. J. Biolumin. Chemilumin.10, 29–34.9.Cree, I.A. et al.(1995) Methotrexate chemosensitivity by ATP luminescence in humanleukemia cell lines and in breast cancer primary cultures: Comparison of the TCA-100assay with a clonogenic assay. AntiCancer Drugs6, 398–404.10.Maehara, Y. et al.(1987) The ATP assay is more sensitive than the succinatedehydrogenase inhibition test for predicting cell viability. Eur. J. Cancer Clin. Oncol.23, 273–6.11.Stanley, P.E. (1986) Extraction of adenosine triphosphate from microbial and somaticcells. Methods Enzymol.133, 14–22.12.Beckers, B. et al.(1986) Application of intracellular ATP determination in lymphocytesfor HLA-typing. J. Biolumin. Chemilumin.1, 47–51.13.Andreotti, P.E. et al.(1995) Chemosensitivity testing of human tumors using amicroplate adenosine triphosphate luminescence assay: Clinical correlation forcisplatin resistance of ovarian carcinoma. Cancer Res. 55, 5276–82.4.D.Related ProductsCell Proliferation ProductsProduct Size Cat.# ApoLive-Glo™ Multiplex Assay10ml G6410 ApoTox-Glo™ Triplex Assay10ml G6320 CellTiter-Fluor™ Cell Viability Assay (fluorescent)10ml G6080 CellTiter-Blue®Cell Viability Assay (resazurin)20ml G8080 CellTiter 96®AQ ueous One SolutionCell Proliferation Assay (MTS, colorimetric)200 assays G3582 CellTiter 96®AQ ueous Non-RadioactiveCell Proliferation Assay (MTS, colorimetric)1,000 assays G5421 CellTiter 96®AQ ueous MTS Reagent Powder1g G1111 CellTiter 96®Non-RadioactiveCell Proliferation Assay (MTT, colorimetric)1,000 assays G4000 Additional sizes available.Cytotoxicity AssaysProduct Size Cat.# CytoTox-Glo™ Cytotoxicity Assay (luminescent)*10ml G9290Mitochondrial ToxGlo™ Assay*10ml G8000 MultiTox-Glo Multiplex Cytotoxicity Assay(luminescent, fluorescent)*10ml G9270 MultiTox-Fluor Multiplex Cytotoxicity Assay(fluorescent)*10ml G9200 CytoTox-Fluor™ Cytotoxicity Assay (fluorescent)*10ml G9260 CytoTox-ONE™ Homogeneous MembraneIntegrity Assay (LDH, fluorometric)*200–800 assays G7890 CytoTox-ONE™ Homogeneous MembraneIntegrity Assay, HTP1,000–4,000 assays G7892 CytoTox 96® Non-Radioactive Cytotoxicity Assay1,000 assays G1780 (LDH, colorimetric)*GSH-Glo™ Glutathione Assay10ml V691150ml V6912 GSH/GSSG-Glo™ Assay10ml V661150ml V6612 *Additional sizes available.LuminometersProduct Size Cat.# GloMax®-Multi+ Detection System with Instinct™ Software:Base Instrument with Shaking 1 each E8032 GloMax®-Multi+ Detection System with Instinct™ Software:Base Instrument with Heating and Shaking 1 each E9032 GloMax®-Multi+ Luminescence Module 1 each E8041Apoptosis ProductsProduct Size Cat.# Caspase-Glo®2 Assay*10ml G0940 Caspase-Glo®6 Assay*10ml G0970 Caspase-Glo®3/7 Assay* 2.5ml G8090 Caspase-Glo®8 Assay* 2.5ml G8200 Caspase-Glo®9 Assay* 2.5ml G8210Apo-ONE®Homogeneous Caspase-3/7 Assay1ml G7792 DeadEnd™ Fluorometric TUNEL System60 reactions G3250 DeadEnd™ Colorimetric TUNEL System20 reactions G7360Anti-ACTIVE®Caspase-3 pAb50µl G7481Anti-PARP p85 Fragment pAb50µl G7341Anti-pS473Akt pAb40µl G7441 Caspase Inhibitor Z-VAD-FMK, 20mM50µl G7231125µl G7232*Additional sizes available.(a)U.S. Pat. Nos. 6,602,677 and 7,241,584, European Pat. No. 1131441, Japanese Pat. Nos. 4537573 and 4520084 and other patents pending(b)U.S. Pat. No. 7,741,067, Japanese Pat. No. 4485470 and other patents pending.(c)U.S. Pat. No. 7,700,310, European Pat. No. 1546374 and other patents pending.(d)U.S. Pat. Nos 7,083,911, 7,452,663 and 7,732,128, European Pat. No. 1383914 and Japanese Pat. Nos. 4125600 and 4275715.(e)The method of recombinant expression of Coleoptera luciferase is covered by U.S. Pat. Nos. 5,583,024, 5,674,713 and 5,700,673.© 2001–2012 Promega Corporation. All Rights Reserved.Anti-ACTIVE, Apo-ONE, Caspase-Glo, CellTiter 96, CellTiter-Blue, CellTiter-Glo, CytoTox 96 and GloMax are registered trademarks of Promega Corporation. ApoTox-Glo, ApoLive-Glo, CellTiter-Fluor, CytoTox-Fluor, CytoTox-Glo, CytoTox-ONE, DeadEnd, GSH-Glo, GSH/GSSG-Glo, Instinct, Mitochondrial ToxGlo and Ultra-Glo are trademarks of Promega Corporation. alamarBlue is a registered trademark of Trek Diagnostic Ssystems, Inc.Products may be covered by pending or issued patents or may have certain limitations. Please visit our Web site for more information.All prices and specifications are subject to change without prior notice.Product claims are subject to change. Please contact Promega Technical Services or access the Promega online catalog for the most up-to-date information on Promega products.。

Quantabio repliQa

Quantabio repliQa

Quantabio, 100 Cummings Center Suite 407J, Beverly, MA 01915IFU-115.1 Rev01repliQa™ HiFi Assembly MixCat. No. 95190-010 95190-050Size:10 reactions 50 reactionsStore at -25°C to -15°CDescriptionThe repliQa™ HiFi Assembly Mix simplifies the construction of recombinant DNA through the simultaneous and seamless assembly of multiple DNA fragments possessing terminal regions of sequence overlap in a single, isothermal reaction. Similar in principle to the Gibson Assembly ® Method 1, the high efficiency repliQa HiFi Assembly Mix is ideal for a range of genetic engineering applications including routine molecular cloning, site-directed mutagenesis, assembly of large constructs for synthetic biology applications, and the construction of diverse sequence libraries for directed evolution studies. The concentrated, two-component format allows flexibility in design of assembly reactions and compatibility with less concentrated DNAsamples. The repliQa Mix has been optimized for use with a total input quantity of DNA fragments in the range of 0.03 to 0.5 pmols. The assembly of up to six DNA fragments is recommended, though the repliQa Mix has been successfully used for more complex assemblies.Double stranded DNA fragments for assembly can be generated by PCR amplification, chemical synthesis, or isolation of restriction fragments. When working with fragments PCR amplified from plasmid vectors, the included DpnI restriction endonuclease can be used for selectively digesting methylated, residual plasmid DNA to reduce background transformants. The repliQa mix is directly compatible with most common E. coli cloning hosts and generally provides a high yield of accurately assembled product.The DNA assembly occurs through the actions of three enzymes:• A non-thermostable 5' to 3' exonuclease that partially eliminates one strand of a DNA duplex to expose complementary overlap regions forhybridization.• A high-fidelity thermostable polymerase that fills the gaps remaining between the hybridized fragments of the overlapping regions.• A thermostable DNA ligase that covalently seals the resulting nicks at fragment junctions, generating double-stranded, assembled DNA moleculessuitable for transformation of cells.ComponentsReagent Description95190-01095190-050 repliQa HiFi Assembly Enzyme Mix Optimized formulation of enzymes for 5’-endresection, high fidelity 3’-end extension, and nick sealing.1 x 0.02 mL1 x 0.10 mLrepliQa 10X Assembly Reaction Buffer 10X reaction buffer containing dNTPs, magnesium, and cofactors.1 x 0.1 mL 1 x 0.50 mLDpnI (20 U/µl)Restriction endonuclease for the (optional) post-PCR digestion of residual unamplified plasmid template.1 x 0.05 ml 1 x 0.25 mlStorage and StabilityStore kit components in a constant temperature freezer at -25°C to -15°C upon receipt. For long term buffer storage (> 30 days) store buffer at -70°C. Refer to the product label or lot-specific Product Specification Sheet (PSF) available at /resources for applicable expiration date.A general diagram of assembly cloning is shown below:Additional reagents and materials that are not supplied• PCR-Grade, nuclease-free water (do not use DEPC-treated water)• High Fidelity DNA Polymerase (Enzymatics VeraSeq TM 2.0, P7511L or equivalent)• A heat block, thermocycler, or water bath capable of holding a temperature of 50 ± 2°C for one hour. • PCR or microcentrifuge reaction tubes.• PCR product purification kit (QIAGEN ® QIAquick ® PCR Purification Kit, 28104 or equivalent). •Competent E. coli cells and accessories as recommended by manufacturer.Before you begin• Design the DNA fragment sequences and assembly strategy. Guidelines are given in Appendix 1.• (Optional) Treat PCR reaction with DpnI if plasmid DNA was used as template for generating DNA fragments to be assembled. (Appendix 2).•(Recommended) After determining PCR fragment or restriction endonuclease-digested fragment size and purity by agarose gel electrophoresis, purify using a spin column-based cleanup or other method. This step is not required but is highly recommended to achieve highest efficiency of fragment assembly.• Measure the concentration of each isolated DNA fragment by absorbance at A 260 or by using a fluorometric quantitation reagent. Agarose gel electrophoresis with mass-calibrated size standards can also be used to quantify fragment mass and quality simultaneously. • Calculate the number of picomoles of each fragment using the following formula:pmols = (weight in ng) x 1000/(bp x 662).• Determine the number of pmols of each fragment to add to the assembly reaction. For cloning, highest efficiencies are achieved with 0.02 to 0.04 pmols of linear vector fragment (50 to 100 ng of 4 kb vector) and 2 to 8-fold molar excess of inserts. • Prepare outgrowth medium and culture plates with appropriate antibiotics for plasmid selection.•Equilibrate the heat block, thermal cycler, or water bath to 50°C for incubation of the assembly reactions .Protocol1. Thaw the repliQa HiFi Assembly Kit components, briefly vortex to mix, and place on ice.2. For each assembly, add reaction components in the order listed in the table below to chilled reaction tubes.The optimal amount of enzyme mix to add per assembly reaction depends on the total quantity of DNA fragments present.ComponentRxn. component volumes (µl) for varying amounts of total DNA≤ 0.125 pmol> 0.125 pmol but ≤ 0.25 pmol > 0.25 pmol Nuclease-free water(17.5 – X) µl (17.0 – X) µl (16.0 – X) µl repliQa 10X Assembly Reaction Buffer 2.0 µl 2.0 µl 2.0 µl DNA fragmentsX µl X µl X µl repliQa HiFi Assembly Enzyme Mix 0.5 µl 1.0 µl 2.0 µl Total volume20 µl20 µl20 µl3. Incubate reactions at 50°C in heat block, thermal cycler with heated lid (set to ~60-80°C), or covered water bath for 1 hr. Hold assembled product mix at 4°C until ready to proceed with transformations. If transformations cannot be performed on the same day, reactions can be stored at -20°C for up to one month.4. Competent E. coli should be transformed, recovered, and plated as per manufacturer guidelines or standard lab practices. Note: If electroporation is to be used for transforming cells, we recommend first diluting the assembly reaction 1:5 in high purity water. There is no need to dilute the assembly reactions prior to transformation of chemically competent cells.5. (Optional) Analyze a portion of the remaining assembly reaction by agarose gel electrophoresis. If DNA fragment assembly occurs properly, a ladder of higher molecular weight DNA bands would be generated.Note: For reactions using three or fewer fragments the incubation time in step 3 can be shortened to 15 minutes.Appendix 1 – Guidelines for Designing DNA Fragments for Assembly1.When designing the DNA fragment sequences and assembly strategy, allow for a region of sequence homology between adjacent DNA fragments.Be sure to avoid regions of repeated bases or repeated short DNA motifs in the design of these overlaps where possible. Regions of secondary structure such as hairpins or stem loops should also be avoided.2.The kit is optimized for the assembly of fragments with overlap regions between 15 – 60 bp. It is recommended that the overlaps be at least 20bp with a minimum of 25% GC content, however overlaps of 30 bp or longer size will provide higher efficiency assembly reactions.3.For generating PCR fragments to be assembled, design primers with a 5’ segment of homology to the adjacent fragment or vector. If the adjacentfragment is also generated by PCR amplification, the overlap can be split between two primers if desired. The 3’ segment of primers should contain sequence specific to the DNA target of interest. Amplify targets using a high-fidelity thermostable DNA polymerase such as VeraSeq 2.0 (Enzymatics, P7511L) or equivalent per manufacturer instructions.4.When designing synthetic gene fragments for assembly, ensure that the 5’ and 3’ segments contain regions of homologous overlap sequencebetween adjacent gene blocks, PCR fragments, or isolated restriction fragments.5.For site-directed mutagenesis applications, the assembly strategy should be designed such that the mutation of interest is centered betweenadjacent PCR fragments. Design the PCR primers as with the standard fragments above, except that the mutation (substitution, insertion, or deletion) should be included within the 5’ segments for both of the adjacent fragments.6.When designing DNA fragments to be assembled with isolated restriction fragments, be aware that any 5’ overlaps from staggered restriction cutswill be eliminated because of the 5’-->3’ nuclease present in the assembly mix, and so should not be included in the measurement of overlap size. If desired, design the 5’ overlap segment of the adjacent fragment to either preserve or eliminate the restriction site.Appendix 2 – DpnI treatment to remove residual plasmid DNAWhen plasmid vector is used as PCR template to generate a fragment for assembly, it is recommended that the reaction be treated with DpnI to eliminate residual methylated plasmid prior to setting up the assembly reaction.1.Add 1 µl DpnI (20U) directly to the PCR reaction (50 µl) following amplification of fragment.2.Incubate at 37°C for 1 hr.3.Heat inactivate DpnI by incubation at 80°C for 20 min.4.(Recommended) Purify the fragment using a spin column-based PCR purification kit.Quality ControlThe repliQa HiFi Assembly Mix is functionally tested for assembly of three 1-kb PCR fragments into 2kb and 3 kb products.The individual components of the repliQa HiFi Assembly Mix are tested to be free of contaminating DNase and RNase.Limited Label LicensesThis product was developed, manufactured, and sold for in vitro use only. The product is not suitable for administration to humans or animals. SDS sheets relevant to this product are available upon request.References1. Gibson, D.G., et al. (2009). Enzymatic assembly of DNA molecules up to several hundred kilobases. Nat. Methods 6, 343-5.。

Kinetix系列低紧急性电动机数据手册说明书

Kinetix系列低紧急性电动机数据手册说明书

SPECIFICATIONSProduct SeriesComponent Type Motion Control Mounting, MotorBrakeFood GradeConnector, Motor EndKeyed ShaftFeedback TypeFeedback Resolution Feedback ProtocolSpeed, RatedSpeed, MaxMagnet Stack LengthFrame SizeVoltage ClassShaft SealSpecial / CustomOutput Torque, Continuous Output Torque, Peak Compatible Drive Series'Rated Power, ContinuousRotor InertiaOperating Temperature, Max Operating Temperature, Min MPL Low InertiaRotary Servo MotorFlange Mount, MetricNo Y / NNoSpeedTec DIN (Type M7)Yes Y / NAbsolute Single-turn typeSin/Cos, 128 cycles/rev resolutionHiperface protocol7000rpm7000rpm20 = 50.8mmFrame 15 / Frame 063 = 63mm size200V ACNo Y / NNo0.49Nm, continuous1.58NmKinetix 5500 (Bul. 2198)Kinetix 6200 / 6500 (Bul. 2094)Kinetix 6000 (Bul. 2094)Kinetix 300 (Bul. 2097)Kinetix 350 (Bul. 2097)Kinetix 2000 (Bul. 2093)Kinetix 7000 (Bul. 2099)Ultra 3000 (Bul. 2098)compatible0.27kW continuous1.3E-05kg m², rotor40°C max0°C min·Continuous stall torque of 0.26 to 163Nm (2.3 to 1440lb-in.)·Peak torque of 0.77 to 278Nm (6.8 to 2460lb-in.)·Integral 24V brake option·Absolute multi-turn and single-turn high resolution, incremental encoder and resolver feedback options·Low-profile, field-reversible motor connectors for minimal servo motor impact on machine design·DIN connector versions allow flexible orientation of connectors and use of a single cable family with all MP-Series motorsRepresentative Photo Only(actual product may vary based on configuration selections)MP SERIES MPL 240V SERVO MOTOR,0.49 N-M,7000 RPM1300 NHP NHP | .au | 0800 NHP NHP | MPLA1520UEJ72AA DatasheetNHP Electrical Engineering ProductsOperating Temperature, MinStorage Temperature, MaxStorage Temperature, MinRelative humidity, minRelative Humidity, MaxHumidity typeWeightIP RatingDetails, IP RatingShock Acceleration (Max.)Shock Duration (Max.)Vibration Acceleration (Max.)Vibration Frequency, Operational (Max.)0°C min70°C max-30°C min5%RH95%RHNon-condensing1.2kgIP50IP66IP50 minimum, without shaft seal; IP66 with optional shaft seal and use of environmentally sealed cable connectors20g6ms2.5g2000HzREFERENCESInstallation Guide:-User Manual:-Manufacturer Datasheet:-Manufacturer Catalogue & Product Selection:-Supplier Declaration of Conformity:-IECEx Certificate-1300 NHP NHP | .au | 0800 NHP NHP | MPLA1520UEJ72AA DatasheetNHP Electrical Engineering Products。

Instruction manual.pdf_1693225695.0476854说明书

Instruction manual.pdf_1693225695.0476854说明书

I. M EASUREMENT OF DC AND AC VOLTAGE AND CURRENT , MEASUREMENTUNCERTAINTY AND ERRORS.M ESUREMENT OF THE PARAMETERS OF DIODES ANDTRANSISTORSTheory:Theory of errors and uncertainty in the measurement. Uncertainty of type A ,type B and C. Definitions of the instrument precision by the producers. Principle of multimeters. Measurement of DC and AC voltage and current. Connection of the multimeter to the tested circuit. Measurement of the effective value of the voltage and current- definitions & principles. Measurement of the effective value alternating voltage/current with or without superimposed direct voltage/current. Shape coefficient, crest factor. Testing of diodes and transistors using the multimeter Principle of the digital frequency measurement. Exercises:1) Get acquainted with Agilent 33220A waveform generator. Set the appropriate load value according tothe resistor used (Utility > Output Setup> Load> 50Ω). ATTENTION: The generator output must be matched to the load impedance for all laboratory tasks.2) Set the generator for harmonic signal output of 2Vpp amplitude and 100 Hz frequency (setting of thegenerator, not measured value on the voltmeter). Connect the rectifier to loaded output according to the schematic. Measure the rectified voltage by available multimeters (using DC mode). Read at least10 measured values. Estimate measurement uncertainty of type A. Estimate the measurementuncertainty of type B based by parameters from datasheets. Determine overall uncertainty of your measurements (type).3) Generate a harmonic, rectangular, triangular, saw tooth and at least one of embedded arbitrarysignals with arbitrary amplitude from the range 1-5 V and frequency from the range 50-300 Hz with the offset equal to zero. Measure voltages for all shapes using both a TRMS voltmeter and simple multimeter with diode rectifier. Explain why the multimeter readings differ for every waveform and amplitude. Use a multimeter also for frequency measurement of every waveform.4) Repeat task 3 for harmonic, rectangular, triangular, saw-tooth waveform with DC offset set to 1V.Measure the output voltage of the generator by TRMS voltmeter in both AC and DC mode. What is the total dissipated power on the resistor load and what is the effective value of the voltage? Hint -Parceval´s theorem.5) Generate a harmonic signal with amplitude 1V and frequency of 5Hz. What is measured by themultimeter? Gradually adjust the frequency 10, 50, 200, 1k, 10k, 25k, 100k, 500kHz and 1MHz. What is measured by the multimeter? Try to explain the multimeter behavior.6) Set the generator for rectangular pulses of 100 Hz repeating frequency and pulse width of 100 s. Setthe low voltage level to 0V. The high level (pulse amplitude) set gradually to 0.02V, 0.2V, 2V. How does the measured rms value change for different peak values of the signal? What voltage value is shown by the multimeter? Is its variation consistent with the changes of the pulse amplitude?Compare your measurement results acquired with other types of multimeters.7) Repeat task 4 for AC and DC current through the load. How can you calculate total power dissipatedon the resistor load from the measured current and resistor’s value? Compare results with those of the task 4.8) Test available diodes using a multimeter and assess whether they passed. What does thismeasurement tell us about the measured diode? Measure also the Graetz bridge9) Measure PN junctions and h21E of available transistors in the active and inverse mode. Comparemeasured results with datasheet values.10) Switch the multimeter to frequency measurement mode. Set the generator to an arbitrary harmonicwaveform of frequency within kHz range. Gradually rise the amplitude from minimum up to 5V.Observe the measured frequency and determine an amplitude threshold, where multimeter starts to measure correctly. Try to explain the results and behavior of the multimerter in frequency measurement mode.Instruments‘ manuals:Multimeter UT 803Multimeter Agilent 34410AMultimeter Agilent 34405AMultimeter Metex 3640Multimeter METEX 3850DGenerator Agilent 33220AStudy materials:Agilent multimeter simulation installation filesWebsite simulating the function of selected instruments - meas-lab.fei.tuke.sk。

Aeroquip Rynglok Tube Repair System TF100-17G 2 由E

Aeroquip Rynglok Tube Repair System TF100-17G 2 由E

• The system of choice foraerospace hydraulic tubing repair • Approved by Boeing, Airbus, major airlines, and all branchesof the U.S. military• The new tube fittingperformance standard2 EATON Aerospace Group TF100-17G August 2019• Accommodates all tubes . . . all thicknesses • Capable of joining any combination of tubing materials• Accommodates tube float up to .40 inches• All metal 6A1-4V titanium alloy construction• Zero leakage with no elastomeric seals• Provides a thermal range of from -65°F to +450°F without thermal hysteresis effects• Unaffected by long term exposure to high temper- ature aerospace fluids• Exceeds tension strength requirements of Boeing BPS-F -142• Provides torsion strength comparable to that of aerospace tube• Exceeds flexure require- ments of MIL -F -85421 and MIL -F -85720• Exceeds burst and impulse capability of aerospace tube• Passes 15 minute fire test with type IIIb low flow rates and vibration per AS1055B• Provides excellent high current lightning strike capability• Approved for repair by all major commercial aircraft manufacturers• Approved for repair by all branches of U.S. Military NAVAIR 01-1A-8USAF T .O. 1-1A-8 NAVAIR 01-1A-20• Offers a wide variety of fitting configurationsincorporated into the U.S. Government distribution system• National Stock Number cross-reference list available upon requestRynglok Fittings Design FeaturesThe superior capability of Eaton’s Rynglok tube joints has been successfullydemonstrated in over 6,000 tests for sealing integrity, flexure fatigue, pressure impulse, burst strength,tensile strength, resistance to torsion, fire and lightning strikeconductivity.Even after undergoing torsion, fire, stress corrosion, impulse,flexure, and thermal shock testing, the Rynglok tube joints exceed the burst strength of the tubing.A Complete Line of Aerospace Permanent, Separable & Specials FittingsBefore Assembly After AssemblyRynglok fitting strength often exceeds the torsional strengthof the tubing.Performance Verification T estingEATON Aerospace Group TF100-17G Augustl 2019 3Rynglok DesignEaton’s Rynglok designmakes it possible to exceed lightning strike requirements by conducting high surface currents “spark free”. The continuous metal contact insures very low electrical resistance which prevents sparking in critical applications such as aircraft fuel tanks.Lightning Strike — Spark-Free ConnectionRynglok SavesTime and MoneyRynglok simplifies inventory and logistics requirements for both production and repair applications. Rynglok is capable of handling the numerous classes of fluid systems found in the aerospace industry. Rynglok fittings are not sensitive to type of tubing used, or wall thicknesses.The Rynglok Advantage• One titanium fitting for all tube materials• No need for different aluminum, CRESS or titanium fittings• One titanium fitting for all wall thicknesses• No need for different 3000, 4000 and 5000 psi fittingsRynglok's simplified repair method greatly reduces repair time. The system is not time sensitive and the installation tool head does not require 360 degree access around the tube to be repaired. With Rynglok there is no need to disconnect long runs of tubing to complete the repair.Rynglok has proven its superior capabilities to repair tube at all pressure ratings used in military and commercial aircraft.T ube O.D. (inch)3/161/45/163/81/25/83/47/811 - 1/41 - 1/2Titanium Rynglok Fitting Pressure Rating (psi)8,0008,0008,0008,0008,0008,0008,0004,0005,0004,0002,500The chart below shows that the pressure rating of the Rynglok fitting exceeds that of a standard aerospace tube.4 EATON Aerospace Group TF100-17G August 2019Rynglok T ooling• One tube diameter - Any tube - One tool. One Rynglok tool assembles all Rynglok fittings for a given tube diameter• Universal tools accommodate bothforward (push) andreverse (pull) installation• Small tool envelope accommodates installa- ation and repair of high density aircraft systems • Minimal tool head wear • No tool assembly required •Rynglok tools require only 180 degree access tomake repairs. Time con- suming line disconnection to accommodate 360degree access is eliminated • Minimal operator training required• Tools are constructed of safe low-stressed ductilematerial• Time is not a factor in the assembly process• Rynglok assembly is simple, repeatable, reliable and safeRynglok Installation T oolingTool kits for the Rynglok Tube Fitting System can be customized to accommodate your specific requirements.The kit shown (RTSK8-02-002) includes everything needed to repair any size tube between 3/16” and 1 - 1/2” diameter.Rynglok T ool KitsRynglok Universal T oolsPUSHForward Mode: Ring is being pushedPULLReverse Mode: Ring is being pulledEATON Aerospace Group TF100-17G Augustl 2019 5Rynglok Fitting System Installation SequencePosition the marking gage on the end of the cut tube. Use a suitable marking pen to make the position and inspection marks.Place the fitting on the tube within the limits of the positioning mark.When using the tool in the reverse mode as shown, position the tool onto the fitting with the tube side of the ring nested into the moveable jaw. If positioned properly, the front end ofthe tool will be in the fitting groove. Make sure that the fittingis bottomed into the tool.Fitting GrooveInspection MarkPosition MarkMoveable Jaw1. Mark the T ube2. Position the Fitting4. Swaging the FittingTo swage the fitting, apply pressure. Upon completion of swaging, release the pressure, the moveable jaw will return to the original position.5. Inspect the InstallationVisually inspect that the ring is fully advanced onto the fitting using the inspection gage. Be sure to verify that the edge of the fitting is within the limits of the inspection mark.The above steps are repeated for each leg of the Rynglok fitting.Inspection MarkPosition MarkFor a more detailed outline of the Rynglok installation sequence see ourinstallation bulletin, TF100-67.6EATON Aerospace Group TF100-17G August 2019Rynglok Fitting Part Number System and How to OrderBasic Part Number Designation1 Tube size is specified in 1/16” increments, (i.e., 08 = 8/16ths or 1/2”)2 Port 2 and3 only required for reducer fittingsNote: Port numbering system is in accordance with AIR 1590.Port No. 15/8” tube sizePort No. 33/8” tube sizePort No. 21/2” tube sizePort No. 11/2” tube sizePort No. 23/8” tube sizePort No. 31/4” tube sizeEATON Aerospace Group TF100-17G Augustl 2019 7R 82121T ( )R 82421T ( )R 81171T ( )( )R 81151T ( )( )R 82171T ( )( )R 82151T ( )( )R 82471T ( )( )R 82451T ( )( )R 83151T ( )( )R 81122T ( )R 81102T ( )R 82122T ( )R 82102T ( )R 82422T ( )R 82402T ( )R 83102T ( )R 81193T ( )( )R R 81144T ( )R )R 81154T ( )( )( )R R 83154T ( )( )( )R 81106T ( )R R 83106T ( )Copyright © 2019 Eaton All Rights ReservedCopying or Editing is Forbidden Form No. TF100-17G August 2019EatonAerospace Group 9650 Jeronimo Road Irvine, California 92618Phone: (949) 452 9500Fax: (949) 452 9555/aerospaceEatonAerospace GroupFluid & Electrical Distribution Division 300 South East AvenueJackson, Michigan 49203-1972 Phone: (517) 787 8121 Fax: (517) 789 2947。

PR702Ed1TechnicalNotes-Tecomak

PR702Ed1TechnicalNotes-Tecomak

BioAir Activated carbon fi ltersChemical decontamination of the air is based on the properties of charcoal obtained from coconut shells and activated by steam at high temperature process. The fi nely porous active carbon has a structure criss-crossed by millions of minute channels and an enormous exchange surface, about 1300 square meters per gram.Air passing through the carbon invades these channels and the chemical substances it contains are captured very effi ciently, owing to their size, by the physical-chemical process defi ned as Adsorption .This process is enhanced by Chemisorption , that is impregnating the carbon with chemical substances to improve the retention of simple, light and linear molecules. Active carbon fi lters can adsorb any chemical compound possessing a molecular weight over 30 and a boiling point higher than 60°C. Some compounds that fall outside these limits are still satisfactorily retained owing to their molecular structure and size.State of the art constructionIn order to obtain the highest degree of effi ciency and fi ltration the design criteria and operation of the cabinet fi tted with active carbon fi lters are of vital importance.It is essential that the air passing through the active carbon fi lter stays there for about 0.1 seconds (residence time) at a linear speed not exceeding 0.5 meters per second in order to obtain a high fi ltration effi ciency, while a mass of carbon of about 13.5 kg per 1000 cubic meters per hour of airfl ow is required to achieve adequate fi ltration capacity.All BioAir fume cupboards are designed to ensure a time of permanence longer than 0.3 seconds and an air speed through the fi lter never higher than 0.5 meters per second.All BioAir fume cupboards, moreover, are equipped with carbon fi lters weighing over three times the required minimum.Environmental friendly Chemical fi ltration based on active carbon makes it possible to install fume hoods in any environment with no need for expensive ducting of exhausted air.Since fume cupboards fi tted with active carbon fi lters recirculate the air within the room, energy is also saved since there is no need to cool or warm fresh air that replaces the air exhausted from the room as with the use of traditional ducted fume cupboards.Types of fi ltersDifferent types of active carbon fi lters are available, some impregnated with chemical substances to enhance their fi ltration capacity when organic molecules with low molecular weight or inorganic gases and vapours are present.1. GENER AL USE (GP): this is the fi lter more commonly used to capture a broadrange of substances, especially vapours of organic solvents. 2. FORMALDEHYDE (FOR): This type of fi lter is impregnated with an oxidising agentto oxidise the formaldehyde. 3. AMMONIA (AMM): The fi lter is impregnated with copper compounds for effectiveremoval of vapours generated by diluted ammonia solutions and of low molecular weight ammines.4. INOR GANIC ACIDS (ACI): This impregnated fi lter neutralises volatile inorganicacid vapours such as chloridric acid, fl uoridric acid and gaseous acids such as sulphur bioxide and nitrogen bioxide.5. MERCAPTANS (SUL): This fi lter is impregnated with potassium iodate for removinglow molecular weight hydrosulfuric acid and mercaptans.6. MERCURY VAPOURS (ACM): This fi lter is impregnated with iodate compoundsto remove mercury vapours and has a degree of effi ciency of up to 5 ppb in the air expelled, starting from a saturated solution.7. ETHER (ETH): Diethyl ether is adsorbed by the specially impregnated and isretained to a satisfactory degree despite its very low boiling point.8. ALCALINE ODOURS (OAL): This fi lter is used to retain odours emanating fromexcretes, urine and other alkaline organic materials.9. ACID ODOURS (OAC): This filter retains acid odours caused by bacterial decomposition, such as cadaverine, putrescine and animal odours.10. MULTILAYER (ML): These filters may be formed by up to three layers of different carbon types and can retain small quantities of verydissimilar compounds.11. R ADIOACTIVE ISOTOPES (ACR): This filter is impregnated with alogenures and is used for removing low radioactive emissioniodides and methyl iodides.12. HEPA (HEP): This filter can be used for trapping thin powdered chemical componds.Carbon filters safety useThe wide range of carbon filters allows to trap a significant percentage of the chemicals handled in the laboratory. Furthermore the Carbon filters are not suitable when massive quantities of substances are used. Avoid use of carbon filters when unknow reactions are carried out or when highly toxic chemicals are used.When Carbon filters are saturated, they do not present any the risk of fire. No spillage of retained substances is reported.Filters replacementThe replacement frequency can be determinated in respect to the amount of chemicals used, the carbon saturation index (see table) and the exposure levels to the used substances.Filters need to be checked at scheduled intervals, using gas pumps equipped with the proper reaction tube. As the exposure limit value is reached, the filter must be replaced. SAFEHOOD series Fume cupboards are equipped with an electrochemical sensor, to monitor the filter performances: the filter needs to be replaced as soon as the relative alarm is activated.If a main spillage occours, it is important to replace immediately the filter as it could be completely saturated.Filters can be easily removed from every BioAir Fume Cupboards. Dispose filters complying to the local waste regulation.Filters specificationBioAir recirculating Fume cupboards use specific filters for the available models, as detailed in the table below:Safehood S600 x 450 x 100n° 1 / 15 kg / 15 kgSafehood 75 (Main filter)530 x 370 x 100n° 1 / 12 kg / 12 kgSafehood 75 (Safety filter)420 x 420 x 40 n° 1 / 4 kg / 4 kgSafehood 120 (Main filter)530 x 370 x 100n° 2 / 12 kg / 24 kgSafehood 120 (Safety filter)420 x 420 x 40 n° 2 / 4 kg / 8 kgSafehood 165 (Main Filter)530 x 370 x 100n° 3 / 12 kg / 36 kgSafehood 165 (Safety filter)420 x 420 x 40 n° 3 / 4 kg / 12 kgHow to orderGENERAL PURPROSE (GP)CP31000CP41000CP21000FORMALDEHYDE (FOR)CP32000CP42000CP22000AMMONIA (AMM)CP33000CP43000CP23000INORGANIC ACID (ACI)CP34000CP44000CP24000MERCAPTANS (Sul)CP34200CP44200CP24200 MERCURY Vapours (ACM)CP37000CP47000On request ETHER (ETH)CP39000CP49000On request ALCALINE ODOURS (OAL)On request On request CP23500ACID ODOURS (OAC)On request On request CP24500 MULTILAYER for SCHOOLS (ML)On request On request CP20000RADIOACTIVE ISOTOPES(ACR)On request On request CP26000 HEPA FILTER (HEP)CP38000Not available On requestCarbon Saturation IndexIn the following table a selection of chemical substances is listed, together with the suggested carbon filter and an indication of the saturation index.This is intended as the percentage in weight of the substance adsorbed on the filter in respect to the weight of the filter itself.Please enquire for fi lters suitable for not listed substances。

nepcon_97_paper-qualifying_to_j1b

nepcon_97_paper-qualifying_to_j1b

QUALIFYING A PROCESS TO J-STD-001BDouglas Pauls, Technical DirectorContamination Studies Laboratories, Inc.IntroductionElectronics manufacturers are faced with the difficult task of proving that a candidate manufacturing process can produce acceptable hardware, either to the customer of the product, or for internal quality control. In the past, assembly level specifications (e.g. MIL-STD-2000A) told you exactly how to go about such a demonstration. It wasn’t always precisely the optimum, but you didn’t have to figure out all of the fine points of the qualification on your own. In our modern era, “how-to” specifications are now evil things and taboo to all involved with them. The users now have to determine many of the process qualification steps on their own, and sadly, many don’t have the faintest idea where to start. This paper addresses some of the fundamentals that have to be considered when qualifying a candidate process to the B revision of J-STD-001.MIL-STD-2000ANo discussion about process qualifications would be complete without briefly touching the venerable MIL-STD-2000A. This was one of the first documents that went about process qualification. A question that is asked frequently by military manufacturers is “What testing do I do now that MIL-STD-2000A has been canceled without replacement?” The answer is MIL-STD-2000A, Appendices A and C, unless told otherwise by your contract officer. My specialty is not contractual law, but my understanding is that the day you signed the contract, the revision in place at that time is the revision you manufacture to. Any changes that come later are immaterial unless the contract is upgraded to the new revision. If you still manufacture to MIL-STD-2000A and the contracts have not been changed, then you still have to do Appendix A and C testing if you want to use a new process. There are many manufacturers who are going through this process even today because from a contractual standpoint, it is the path of least resistance. A great deal more information on this topic can be found in IPC-TP-1090.J-STD-001, Revision AJ-STD-001, Revision A was developed about the same time as MIL-STD-2000B. MIL-STD-2000B died a political death in Washington, but the two documents were very similar. With the exception of a few commas, the process qualification protocol in J1A was identical to that proposed for MIL-STD-2000B, and has been used as an acceptable protocol since J1A was implemented (January 1995). IPC-TP-1090 also discusses J1A process qualification.The salient points to take from the J1A process qualification are as follows:•Appendix D (SIR) and Appendix F (Ionics) are the qualification protocols•Test Substrate: IPC-B-36 standard test assembly (others possible but seldom used)•Metalization: bare copper, no OSPs•Solder Mask: minimal solder mask only as LCC standoff (bumps)•Starting cleanliness: Precleaned to less than 1 ug NaCl equivalence per square inch•Components: Four 68 I/O LCCs on each test board (5 mil standoff)•Number of SIR test patterns: 10 SIR patterns per board•Sample Size: 3 unprocessed controls, 3 candidate process for both SIR and Ionics •Coating: None•Ionics: Automated ionic cleanliness testers•Ionics Pass / Fail: Historical 10 ug/in2 NaCl equivalence•SIR: Seven days at 85C/85% RH, 50 volt bias, 100 volt measure (method 2.6.3.3A)•SIR Pass / Fail: 100 megohms on all patterns, measured at 96 and 168 hours, 500 megohms at the final ambient reading, no corrosion or metal migration.If your candidate process had ROSE values less than 10 ug NaCl equivalence per square inch (adjusted to machine type), and the candidate boards passed the requirements of the SIR testing, then you could use the new manufacturing process on your product. J1A represented a somewhat improved (depending on who you talk to) method of examining a candidate process and determining some level of minimum performance.A frequently asked question has been “if I qualified to the A revision (J1A), must I do the more complex testing of J1B?”. The answer is no, there is a grandfather clause. See the note in J-STD-001B, paragraph 4.2. Of course, your customers can always force you to redo the testing.Philosophy Change - J1A to J1BJ1B took a radically different approach to specifications. For many years, specifications dictated exactly how something was done. Choices were very limited and the resultant data was not open to much interpretation. Many people have this concept ingrained into them. With the DoD move away from “how-to” specifications to performance based specifications, a manufacturer now has a greater freedom or flexibility, but now has to figure out many of the background issues. Many companies are struggling with the concept.IPC-TR-467, published by Jim Maguire, Boeing, and myself, details some of the rationale for the approaches taken in J1B, Appendix D. There is a complete change in philosophy between J1A and J1B. In J1A, we took a precleaned standard substrate, so we had no outside effects, processed the substrate through our reflow operations, and tested it. This was fine, as far as it went. Many manufacturers were able to discriminate between good and bad processes doing so? But inevitably, the questions were raised:•The B-36 board is nothing like my product. How applicable is the test data?•I have my own internal test vehicle. Why can’t I use that?•The B-36 has very little solder mask and bare copper metal. It is nothing like my SMOBC boards with HASLed tin-lead. Why use it?•The B-36 is pre-cleaned. I don’t preclean my bare boards. What about fabrication residues?•What about interactions between different fluxes (HASL, paste, wave, touchup)?•What about compatibility issues between cleaners and masks, fluxes and masks, etc.?•I normally conformally coat my boards. Why don’t I coat the B-36?•My product functions in a condensing environment. Why do I test the coupon in a static (non-condensing) environment?All very valid questions and deserving of answers. There is no perfect “one size fits all” test protocol. Having a standard substrate allows you to have a set pass/fail level and compare different processes, but there was often a wide gap between the substrate and the product it was supposedly representing. Having a tailored substrate allowed you to be much more representative of product, but the interpretation of data was open to engineering judgment and often subjective. With the Appendix D protocol in J1B, the best of both worlds was attempted.J-STD-001B, Appendix DLet us take a look at the salient points of J1B, Appendix D. A comparison to J1A levels is shown in Table 1.•Appendix D is the only qualification protocol•Test Substrate: Defaults to an IPC-B-36 standard test assembly, but alternative vehicles allowed and encouraged - must be representative of product•Metalization: whatever is used on your product•Solder Mask: whatever is used on your product, but the solder mask cannot cover SIR test patterns.•Starting cleanliness: No precleaning. Test vehicle retains all residues from fabrication •Components: Usually required, but depends on test vehicle•Number of SIR test patterns: depends on the test vehicle•Sample Size: 10 boards for each process combination•Coating: if your product is coated, your test vehicle is coated.•Ionics test: Recommended, but not required•Ionics Pass / Fail (if used): 10 ug/in2 NaCl equivalence as a default, can be specified otherwise•SIR profile: to be chosen by manufacturer as most representative of product•SIR Pass / Fail: related back to equivalent patterns on the IPC-B-36 board, depends on data set means of minimum values and variability of data set.• no corrosion•no metal migration bridging more than 20% of the spacing•if testing coated product, no failures of the coating (adhesion loss, cracking, reversion, etc.).The entire approach in J1B is that just as your product is the sum of the residues of your manufacturing operations, so should your test vehicle represent that sum of residues, and more importantly, the effects of sum of the residues. If you have the most tightly controlled no-clean assembly operation in the world, but your incoming boards are loaded with detrimental residues, it is highly likely that your products are in jeopardy. If you have a solder mask that is incompatible with one of your cleaning agents in a later operation, you have a problem. The J1B approach is designed to look for these “gotchas”.Where To StartThe best place to start is to determine if you have to do the qualification testing outlined in Appendix D. Such testing is done:•When your customer requires it. After all, your customer drives the bus, even if they don’t have a road map and should not have a license.•When your customer feels that the Appendix D testing is the only acceptable way to demonstrate the Materials Compatibility requirement of J-STD-001B, paragraph 3.4.•If you are using a flux that is not contained in the following J-STD-004 designations: RO (L0 or L1), RE(L0 or L1), OR(L0 or L1). This requirement is found in J-STD-001B, paragraph 4.2.•When you are making a change to a proven (qualified) process. How much of a change requires re-testing is up for debate.The fine points of when to do testing could be a paper in itself; so we will proceed with the assumption that you will be doing the testing, for whatever reason.The FabricatorA major new element to process qualification is the introduction of the question of fabrication residues and their effects. A large assembler might logically ask “must I do the qualification testing for each of my 20 bare board suppliers?”; usually with a sinking feeling in the stomach. The answer is potentially yes and could therefore get very expensive. At this point, the assembler should be asking the following questions:•Do I really need all those fabricators? Can I pare it down to a more reasonable value?•How well do I know the incoming cleanliness condition of my bare boards?•Have I ever looked at bare board cleanliness?•Are there seasonal variations or lot-to-lot variations to the cleanliness of the bare boards?•Have the traditional ionic cleanliness tests or Bellcore tests been sufficient to allow me to differentiate good from bad bare boards (residue-wise)?Again, the answering of these questions could fill volumes, and could be approached in many different ways. It is highly recommended that you do testing of bare board cleanliness by ion chromatography per IPC-TM-650, method 2.3.28. This is a far better indicator of bare board cleanliness than any other method available. For bare board cleanliness tests, you can use actual product.Let us proceed with the assumption that you know the cleanliness levels of your bare boards and have chosen your “worst case” fabricator. Most process evaluation methods are similar in that if you look at the worst case situation and can pass the requirements, then it can be assumed that you will pass the less stringent cases as well.The Test VehicleNow that you have chosen which fabricator(s) to use, you must select the test vehicle. The default test vehicle is the IPC-B-36 standard test assembly. The manufacturer must determine how representative the B-36 is of the actual product. In many cases, the B-36 is significantly different from actual product. There are other test vehicles available in the industry for use as a qualification vehicle, or you can design your own vehicle. Other vehicles include:•Boeing qualification board (primarily PTH)•NASA Test Assembly (mixed technology)•Low Residue Soldering Task Force (LRSTF) test assembly (mixed technology)•ARPA ETC’96 Test Board (mixed technology)•Series of boards from TopLine (e.g. Sabre boards)• Solectron board•Not recommended - IPC-B-24, IPC-B-25, IPC-B-25AWhatever is chosen, the vehicle must have the following characteristics.•The vehicle must be representative of the product and be amenable to SIR testing•The test patterns and components must be representative of the hardest / greatest challenge on your product, e.g. if you do 15 mil pitch SMT, your test vehicle should have 15 mil pitch.•It should contain the same material mix as on your product, e.g. if your product has tin-lead SMOBC on FR-4, your test vehicle should too.•The SIR test patterns under the components must not be covered with solder maskYou will need to know the number of “squares” in the representative SIR test patterns to determine the SIR pass fail numbers related back to the IPC-B-36 test board.Solder Mask and MetalizationNow you have your fabricator chosen and your fabricator now has your Gerber files for the test board in hand. You must choose the solder mask and metalization that will go on your test assembly. At this point, the following question will probably be raised:“Do I need to do qualification testing for every combination of solder mask and metalization?”Again, potentially yes and potentially very expensive. Just as before, you should look very hard at your mix of solder masks. Do you really need that many? The same thought applies for the metalization involved. If most of your product is liquid photoimageable (LPI), then that is what should go on your vehicle. If most of your product is HASLed, then your test vehicles should be as well.The selection of solder mask and metalization should be from a designed study. If you are trying to use the “worst case” approach, a designed study is the only way to do so. At some point in the future, it is likely that your customer will want to see data on how you chose the mask-metalization combination for testing. A scientific study looks much better than showing them the dart board.Fabricating the VehiclesNow that you have chosen the fabricator, laminate, solder mask, and metalization, it is time for your fabricator to make the test boards. The boards should be made in the same way as your product. There must also be no special cleaning steps (precleaning) that are not part of the normal fabrication process.You will need to know the number of boards to be made. You will need to have 10 test samples for each combination of materials and processes that you wish to qualify. Example: if you have chosen one product line of CEM-1, LPI mask, tin-lead and a second product line of FR-4, LPI mask, OSP coated, to go through your assembly process, then you will need 20 boards (at least). Ten boards for the first product line and ten boards for the second product line.Since you get better prices from volume discounts, order lots. You can use the other boards for preliminary studies and for the inevitable goofs in manufacturing.Assembly ProcessNow you have the fabricated test boards, and presumably the test components, in house, ready to subject them to the assembly process. The rule to follow is “if your product sees it, the test board sees it”. This includes exposure to mounting adhesives, temporary solder masks, solder paste, solder flux, hand soldering with cored wire solder (and additional flux if that’s what you do on product). Any interim cleaning steps, such as brushing with isopropanol, or a final cleaning prior to conformal coating, must also be performed.Conformal CoatingNow the manufacturer must choose whether or not to conformally coat the test boards. If the product is coated, the test board is coated. If you do not conformally coat the product, then the test board is not coated. Again, you face the potential of having to do the testing for all your coatings, and determining if you need all those coatings. Each coating can represent a harmful interaction with existing residues. Only preliminary studies can determine if there are hazardous situations with any of your coatings or coating processes.One note of caution from a test lab professional, if you coat the entire board, including the points we need to attach to for SIR testing, and we have to then scrape the coating off to get a good connection, we scream loudly and go for your pocketbook. You may need to mask off these connection points during the coating process or include test lead attachment as part of the assembly process. A competent test lab should be able to assist with this area (I know of a good one in Kokomo).The Test EnvironmentThe last choice the manufacturer has is the choice of the SIR test environment: cyclic or static. The cyclic method has the environment cycle between 25C and 65C, 90% RH, three times perday, for ten days. This method simulates a condensing environment and is most applicable to conformally coated product, or uncoated product that will likely see condensation during it’s life cycle. The static method has a constant 65C / 85% RH environment over a 7 day period. This method is more applicable for testing for corrosion and metal migration in uncoated product, or for product where condensation is not likely.While the choice is up to the manufacturer, it is recommended that the coated boards be tested with the cyclic profile and the uncoated boards be tested with the static method.The SIR TestUnfortunately, SIR testing is still a technique dependent test. IPC-9201 can help educate both the tester and the manufacturer on the many factors which affect SIR testing. This becomes important now because the pass-fail criteria for SIR testing includes the variability of your data set as a factor. In previous SIR qualification protocols, all you were concerned about was a minimum value. If you had a wide variation to the data, it did not make a difference. Now it does. The pass-fail criteria looks at both minimum values and the standard deviation of the data set.Choose a test lab that knows SIR testing well. They should be able to show you how controlled their chambers are; repeatability studies for SIR, calibration data for SIR, chamber water cleanliness, etc.Why should you be concerned about all of these things? If your SIR tester does not know what he/she is doing, the test variability can overshadow all the work you have done in the process development. A poor test technique could fail your qualification more than your process parameters.Calculating the Pass Fail CriteriaAll of the pass-fail SIR criteria for J1B is related back to a comparable pattern on the IPC-B-36 test board. Let us say that we use a simple test PWB with only one SIR pattern per PWA; a “Y” pattern under the most difficult to clean part on each test assembly. This “Y” pattern has a “gap”25.4 mm long * .635 mm spacing = 25.4/0.635 = 40 squares(1 inch long * 0.025 inch spacing = 40 squares)The equivalent pattern for a B-36 would be pattern M6, M7, M9, or M10. Each of these patterns have the same pattern characteristics:68.58 mm long * 0.152 mm spacing = 68.58 / 0.152 = 450 squares(2.7” long * 0.006” spacing)Our new pass-fail level for our “Y” pattern = 100 megohms * (450 / 40) = 1,125 megohms or 9.05 on the log scale.Example Data SetProcess PWA T0M1M2M3M4M5M6M7TF C101 3.21E+13 6.54E+10 5.16E+10 4.65E+10 4.10E+10 3.39E+102.75E+102.26E+107.77E+11C1027.08E+12 2.01E+10 2.23E+10 2.17E+10 2.01E+10 1.86E+101.69E+101.56E+10 1.12E+12C103 1.21E+12 4.00E+09 4.23E+09 4.18E+09 4.23E+09 4.14E+094.09E+094.03E+09 4.68E+11C104 4.21E+11 1.32E+10 1.56E+10 1.51E+10 1.45E+10 1.38E+101.32E+101.29E+10 1.78E+12C1059.40E+11 1.16E+10 1.18E+10 1.05E+109.57E+098.74E+097.98E+097.45E+09 5.09E+11C106 3.62E+13 2.94E+10 1.33E+10 6.30E+09 4.56E+09 3.04E+092.85E+092.86E+09 1.13E+12C107 6.73E+12 6.24E+11 3.57E+11 4.31E+10 1.63E+109.59E+097.90E+096.91E+09 3.42E+12C1087.33E+12 6.12E+11 1.94E+118.96E+10 5.65E+10 4.13E+102.80E+102.28E+10 3.08E+12C109 5.13E+12 1.83E+10 1.65E+10 1.53E+10 1.45E+10 1.37E+101.29E+101.27E+10 3.49E+12C1108.26E+11 1.03E+10 1.25E+10 1.17E+10 1.10E+10 1.01E+109.42E+099.05E+09 4.66E+13Let us say that the above table is the data generated for our 10 test boards. T0 represents initial ambient measurements. T f represents final ambient measurements. All other measurements are made at the elevated temperature and humidity conditions of the chosen test method. We are interested only in the minimum values for the test pattern over the course of the test. Those values appear in bold face. If we made a table of these minimum (also called WetMin) numbers, we would have the following.Process PWA WetMin LogOhmC101 2.26E+1010.35C102 1.56E+1010.20C103 4.00E+099.60C104 1.29E+1010.11C1057.45E+099.87C106 2.85E+099.45C107 6.91E+099.83C108 2.28E+1010.36C109 1.27E+1010.10C1109.05E+099.96Mean9.98Standard Deviation0.30From the geometric mean of the WetMin values (9.98) we subtract three standard deviations:9.98 - 3*(0.30) = 9.08.Our calculated pass-fail number is 9.05. Since 9.08 > 9.05, our candidate process passes the test, at least numerically. If there is corrosion or metal migration (which bridges more than 20% of the spacing) found on the SIR test pattern after testing, then the test fails.Summary of Choices to Be MadeThe choices facing the assembler qualifying to J-STD-001B are:•selection of fabricator•selection of test vehicle and SIR patterns on test vehicle•selection of metalization•selection of solder mask•selection of assembly process parameters•selection of coated or uncoated samples•selection of the SIR temperature - humidity profileEach selection can have a major impact on both the qualification testing and on your product. Each selection should reflect the choices made for actual hardware.Summary of Preliminary Studies RecommendedFor the assembler facing this array of choices, I recommend the following preliminary studies:•Bare board cleanliness study for the fabricators by ion chromatography. The use of the classical ionic cleanliness testers will not give you enough relevant information.•Compatibility studies between masks / metalizations and your assembly process. Both SIR and ion chromatography can be used for this.•Investigate different SIR vehicles to determine which is most representative of your product and to establish baseline responses for the vehicle.•Do some dry runs on a limited number of samples to see if you are near passive, before doing a large scale qualification test.•If you are a large corporation, or use a high mix of materials, ask yourself candidly if you really need that many materials.Other Resources AvailableThe new approach to process qualification will undoubtedly bewilder many people (it bewildered me, an I helped write it). Here are some other resources to aid in your background investigations:•Drafts of the IPC-J-STD-001 Handbook (will eventually compliment the standard when completed)•Course - Understanding the Importance of the National Soldering Standard - taught by Rosser, Hymes, and Maguire•IPC-TR-1090, “The Layman’s Guide to Qualifying New Fluxes to MIL-STD-2000A and J-STD-001A”• IPC-TR-467•EMPF No-Clean Technology Course• A second “Layman’s Guide” for J1B. I anticipate finishing it in March of 97.。

胰岛素受体英文优质PPT资料

胰岛素受体英文优质PPT资料

taining IR485 pre-saturated with a taining IR485 pre-saturated with a taining IR485 pre-saturated with a labels) correspond to the injection of the respective Ala-substituted of the respective Ala-substituted 关键氨基酸:ɑCT上的His710,Phe714 αCT(704-719) peptide into a cell Control titrations αCT(704-719) peptide into a cell αCT(704-719) peptide αCT(704-719) peptide into a cell
The first ten ITC curves (mauve labels) correspond to the injection of the respective Ala-substituted αCT(704-719) peptide into a cell containing the mini-receptor IR485, the remaining eight (orange labels) correspond to the injection of zincfree porcine insulin into a cell containing IR485 pre-saturated with a 10× molar concentration of the respective Ala-substituted αCT (704-719) peptide. Control titrations (lower right) employed the native αCT(704-719) peptide
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PRA-HEP/97-7 Jet rates in deep inelastic scattering:wherefrom comes the sensitivity toαs?Jiˇr´ıCh´y la and Jiˇr´ıRameˇsInstitute of Physics,Academy of Sciences of the Czech Republic,Prague1AbstractFor theoretically consistent determination ofαs from jet rates in deep inelastic scattering the dependence onαs of parton distribution functions is in principle as important as that of hard scattering cross–sections.For the kinematical region accessible at HERA we investigate in detail numerical importance of these two sources of theαs dependence of jet rates.1IntroductionOne of the problems of quantitative determination of the running ofαs is related to the fact that it usually requires combining results of different experiments in different kinematical regions.Recently the H1[1]and ZEUS[2]Collaborations have reported evidence for the running ofαs(µ)obtained from the measurement of jet rates in deep inelastic scattering(DIS)via the quantityR2+1(Q2)≡σ2+1(Q2)σ1+1(Q)+σ2+1(Q),(1)whereσk+1denotes the cross–section for the production of k hard and one proton remnant jets. There are now several NLO Monte–Carlo generators[3,4,5],suitable for analyses of jet production in DIS.In this paper we shall concentrate on the H1analysis[1]which,using PROJET4.1[3]with the JADE jet algorithm and y c=0.02,obtained the following result forαs(M Z,MS)αs(M Z,MS)=0.123±0.012(stat.)±0.008(syst.).(2) In JADE cluster algorithm,the jet resolution parameter y c is defined as y c=(p i+p j)2/W2,where p i,p j are parton momenta and W2=Q2(1−x)/x stands for the square of theγp CMS energy. The result(2)has been extracted from the Q2–dependence of R2+1(Q2),displayed in Fig.2of[1], using only the two highest Q2data points.Within the error bars the value(2)is consistent with the world average,but its accuracy is insufficient to draw anyfirmer conclusions.In the procedureadopted in[1]αs(µ,MS)(or,equivalently,ΛMS )was considered as a free parameter in the hardscattering cross–sections,but not in the parton distribution functions(PDF),for which the MRSH set was used.However,as each set of PDF has a particular value ofΛbuilt in,one must checkfor the consistency between this inputΛMS and the output one,obtained from comparison of(1)with data.Clearly,in a consistent determination ofαs,ΛMS must be varied simultaneously in PDFand parton level hard scattering cross–sections.In practical applications to physical quantities involving beside the hard scattering cross–sections also parton distribution and/or fragmentation functions it is often useful to know wherefrom comes most of the sensitivity toαs.The purpose of our paper is to investigate this question in detail for the jet rates(1).1e–mail:chyla@fzu.cz,rames@fzu.cz1Throughout this paper we stay in the conventional MS renormalization scheme(RS)of the couplant a≡αs(µ)/πand omit therefore the specification“MS”inΛas well as inαs(µ,MS). The jet cross–sectionsσk+1in(1)are given as convolutionsσk+1(Q2,y c,Λ)≡i 1d xf i(x,M,Λ)C k+1,i(Q,M,x,y c,Λ)(3)of the parton level cross–sections C k+1,i and PDF f i(x,M),evaluated at the factorization scale M. The sum runs over all parton species i.In perturbative QCD C k+1,i are given as expansions in the couplant a(µ/Λ),taken at the hard scattering scattering scale2µ.To the NLO we haveC2+1,i(Q,M,x,y c,Λ)=a(µ/Λ)c(1)2+1,i(Q2,x,y c)+a(µ/Λ)c(2)2+1,i(Q,M,x,y c),C1+1,i(Q,M,x,y c,Λ)=c(0)1+1,i(Q,x)+a(µ/Λ)c(1)1+1,i(Q,M,x,y c).(4)In standard global analyses of hard scattering processes[7,8,9],Λisfitted together with a set of parameters a(j)i,describing distribution functions p(j)(x,M)of parton species j at some initial scale M0,usually in the formp(j)(x,M0)=a(j)0x a(j)1(1−x)a(j)21+a(j)3√x+a(j)4x+a(j)5x3/2.(5)Writing the derivative dσ2+1/d lnΛasdσ2+1(Q2,Λ)d lnΛ=i 1d xd f i(x,M,Λ)d lnΛa(M)c(1)2+1,i(x)+f i(x,M,Λ)c(1)2+1,i(x)d a(M)d lnΛ=a(M)ij 1d x−1d yyf j(y,M,Λ)P(0)ij(z)a(M)c(1)2+1,i(x)+bf i(x,M,Λ)a(M)c(1)2+1,i(x),(6)where z≡x/y and P(0)ij (z)are the LO branching functions3,we see that the leading order termof dσ2+1/d lnΛgets contributions from the variation ofΛin both the PDF f i and hard scattering cross–sections C2+1,i.The two terms in the brackets of(6)are of the same order and their relative importance thus is basically a LO effect.For the quantity R2+1(Q2)the situation is less obvious.PDF appear in both the numerator and denominator of(1)and so some cancellations might occur,while the hard scattering cross–sections start as O(a)for C2+1,i and as O(1)for C1+1,i.Nevertheless a detailed analysis[10]shows that also for the ratio R2+1varyingΛin PDF generates terms which are of the same order as those resulting from the variation ofΛin the hard scattering cross-sections C k+1,i.2Parton distribution functions for arbitraryΛTo assess the potential of(1)for a precise determination ofαs we wish to separate the question of its sensitivity toαs from the sensitivity to parameters describing the initial condition on the PDF.2Although in generalµ=M,we shall follow the usual practice and setµ=M.3In(6)we have for brevity suppressed the dependence of c(1)2+1,ion y c and written a(M/Λ)simply as a(M).2Moreover,in order to investigate the numerical importance of varyingΛin PDF we have to know what to do with the parameters M0,a(j)i in(5)whenΛis varied.We cannot keep themfixed as this would contradict the idea of factorization.To see why,let usfirst consider the couplant as well as the evolution equation for the nonsinglet quark distribution function q NS(x,M),at the LO.In terms of conventional moments we haved q NS(n,M,Λ)d ln M =a(M/Λ)q NS(n,M)P(0)NS(n),d n≡−P(0)NS(n)/b,(7)whenceq NS(n,M,Λ)=A n[a(M/Λ)]d n,a(M/Λ)=1b ln(M/Λ).(8)In the above expressions P(0)NS (n,M)are moments of LO nonsinglet branching function and A n areunique dimensionless constants,describing the nonperturbative properties of the nucleon,intro-duced in[11].Via(8)they determine the asymptotic behavior of q NS(n,M,Λ)for M→∞and thus provide alternative way of specifying the initial conditions on the solutions of(7).The sepa-ration in(8)of q NS(n,M,Λ)into two parts–one calculable in perturbation theory and the other incorporating all the nonperturbative effects–is the very essence of the factorization idea.Note that in(8)the dependence onΛis simply a reflection of its dependence on M.Knowing the latter, we know the former.Eq.(8)implies that we can write down the equations for theΛ–dependence of PDF which are very similar to standard evolution equations,describing their dependence on the factorization scale M.The situation is basically the same as for the running couplant a(M/Λ)for which d a(M/Λ)/d lnΛ=−d a(M/Λ)/d ln M.In the case of PDF the only difference stems from the necessity to properly specify the initial conditions on the solution of(7).Forfinite initial M0 (8)impliesq NS(n,M,Λ)=q NS(n,M0,Λ)a(M/Λ)a(M0/Λ)dn=q NS(n,M0,Λ)exp(−d n s),(9)wheres≡lnln(M/Λ)ln(M0/Λ).=lna(M0/Λ)a(M/Λ)(10)is the so called“evolution distance”[9].The second equality in(10)holds exactly at the leading order and approximately at higher ones.Rewriting(9)again in the form(8)q NS(n,M,Λ)=q NS(n,M0,Λ)(a(M0/Λ))d n(a(M/Λ))d n(11)we see that the ratio of q NS(n,M0,Λ)and(a(M0/Λ))d n equals A n and must therefore be both M0 andΛindependent.This,however,is possible only if the initial moments q NS(n,M0,Λ)do,as indicated,depend beside M0onΛas well!Note that considering q NS(n,M,Λ)as a function of s,formula(11)implies that entire dependence of q NS(n,M,Λ)onΛcomes solely from the term ln(M/Λ)=1/a(M/Λ)in(10)!The same happens in the realistic case of coupled quark and gluon evolution equations[12].If we wish to investigate the dependence of PDF solely onΛ,keeping fixed all other parameters,specifying the initial conditions on PDF,we cannotfix initial conditions at somefinite M0,(i.e.the parameters p(j)(x,M0)in(5)).It is the constants A n that must be kept fixed instead!On the other hand,in global analyses,like[7,8,9],all parameters,includingΛ,are varied simultaneously andfitted to data.In these circumstances it is then not straightforward to determine the sensitivity of a given physical quantity toαs itself.3The preceding paragraph also suggests a simple procedure,which makes use of some of the available parameterizations and generalizes them to arbitraryΛ,keeping the constants A nfixed. From all the available parameterizations of PDF those given by analytic expressions of the coef-ficients a(j)i on a general factorization scale M via the variable s are particularly suitable for this purpose.In our studies we took several of the GRV parameterizations,both LO and NLO ones, defined in[13].At the LO the recipe for construction of PDF for arbitraryΛis simple:•Use any of these parameterizations withfitted value ofΛfit.•KeepΛin ln(M0/Λ)fixed at the valueΛfit.•VaryΛin ln(M/Λ).•Use the original parameterization with the redefined s=s(Λ).This construction is exact at the LO.At the NLO the couplant a(M/Λ)is no longer given simply as 1/ln(M/Λ)and consequently the second equality in(10)holds only approximately.This,together with the additional term appearing in the NLO expression for q NS(n,M,Λ)q NS(n,M,Λ,A n)=A na(M/Λ)1+ca(M/Λ)dn(1+ca(M/Λ))P(1)NS(n)/bc,(12)destroy simple dependence of q NS on M,M0andΛvia the variable ing the above recipe for the NLO GRV parameterizations provides therefore merely an approximate solution of our task, but one that is sufficient for the purposes of determining the relative importance of varyingΛin PDF and hard scattering cross–sections as this relative importance is basically a LO effect.As an illustration of our procedure we plot in Fig.1,for x≥10−4and two values of Q2, the dependence of valence and sea u–quark and gluon distribution functions onΛ.The curves correspond to the LO GRV parameterization of[13].We see that this dependence decreases with increasing Q2,is most pronounced for the gluon distribution function and almost irrelevant for the valence quark one.These features are qualitatively the same as those obtained in refs.[14,15], which contain results of globalfits performed for severalfixed values ofΛ.Quantitatively,however, the sensitivity to the variation ofΛ,observed in these papers,is markedly weaker than that displayed in Fig. 1.This is due to the fact that ourΛ–dependent PDF are not constructed to describe the hard scattering data for all values ofΛ(they do so by definition only forΛ=Λfit) but in order to facilitate studies of the dependence of physical quantities solely onΛ,with the appropriate parameters specifying the initial conditions keptfixed.On the other hand,in global analyses of[14,15]fitting the data for different values ofΛleads to different values of boundary condition parameters a(j)i at M0,which partially compensates the variation ofΛ.3Numerical resultsAll the results reported below were obtained using the PROJET4.1generator[3].It is true that the JADE jet algorithm used in this program has certain theoretical shortcomings,but as the H1 Collaboration used it,we did the same.Although MC generator MEPJET[4]is to be preferred on theoretical grounds,the main features of our results are unlikely to change because theΛ-dependence of R2+1is basically a LO effect.To quantify the dependence of R2+1onΛseparately in hard scattering cross–sections and PDF we consider it as a function of Q2,y c and two independent Λ–parameters,denoted asΛhsc andΛpdf respectively.The results are then studied as a function of Λhsc,Λpdf,Q2and y c for4Figure1:The dependence of xu v(x,Q2),xu sea(x,Q2)and xG(x,Q2)of the valueΛpdf according to the recipe described in the text and for two values of Q2.At low x,the curves correspond from above to the values ofΛpdf,subsequently,0.1,0.2,0.3,0.4and0.5.5Figure2:The ratio R2+1(Q,y c,Λpdf,Λhsc)as a function ofΛpdf forfixedΛhsc and a series of Q2values(solid lines),or as a function ofΛhsc forfixedΛpdf and the same set of Q2values (dotted lines).The dashed lines correspond to simultaneous variation ofΛpdf=Λhsc.Solid curves correspond,from below,tofixedΛhsc=0.1,0.2,0.3,0.4,0.5and the dotted to the samefixed values ofΛpdf.In all plots y c equals0.01.•12values of Q2(equidistant in ln Q2)between5and104GeV2,•5values ofΛpdf orΛhsc,equal to0.1,0.2,0.3,0.4and0.5GeV,•3values of y c=0.01,0.02,0.04.3.1No cuts on jetsFirst we analyse the case with no cuts on thefinal state jets and then discuss the changes caused by the imposition of cuts as specified in[1].Fig.2shows a series of plots corresponding to y c=0.01and displaying the dependence of R NLO2+1onΛhsc forfixedΛpdf(dotted curves)or onΛpdf forfixedΛhsc(solid curves).Each plot corresponds to one of the6selected values of Q2.We see that for Q2below about40GeV2the solid curves are steeper that the dotted ones,while above40GeV2 the situation is reversed.This means that below40GeV2varyingΛin PDF is more important than varying it in the hard scattering cross–sections for Q2,while the opposite holds above406Figure3:(a–c)Q2–dependence of the ratio R2+1(Q,y c,Λpdf,Λhsc)forfixedΛpdf=0.1,0.3,0.5 GeV andfive values ofΛhsc=0.1,0.2,0.3,0.4,0,5GeV.(d–f)The role ofΛpdf andΛhsc is reversed.No cuts were applied in evaluating R2+1and y c=0.01.In all plots the curves are ordered from below according to increasingΛhsc(in a–c)orΛpdf(in d–f).GeV2.The same information as in Fig.2is displayed in a different manner in Fig.3,where the Q2dependence of R2+1is plotted for various combinations ofΛpdf andΛhsc.The shape of the curves in Fig.3is a result of two opposite effects:as Q2increases the phase space available for produced jets increases as well,but at the same time the value of the runningαs(Q/Λ)decreases. At low Q2,on the other hand,phase space shrinks,butαs(Q/Λ)grows.In Fig.3the relative importance of varyingΛpdf andΛhsc is reflected in a bigger spread of the five curves in Figs.3d)-f)compared to those in Fig.3a)-c)for Q2≤40GeV2and smaller spread above40GeV2.Note also that forfixedΛpdf the sensitivity to the variation ofΛhsc is about the same at all Q2.The shape of curves in Fig.2suggests that the ratioV(Q2,y c,r,s)≡R2+1(Q2,y c,Λpdf=s,Λhsc=r)R2+1(Q,y c,Λ=r,Λ=s),(13)is approximately a linear function of s for anyfixed Q2,y c,r.Considered as a function of s forfixed r,(13)quantifies the relative importance of varyingΛin PDF and hard scattering cross–sections.7Figure4:(a–c)The quantity W(Q2,y c,r)as a function of Q2forfive values of r(given in GeV) and y c=0.01,0.02,0.04.All curves correspond to the case of no cuts.To summarize the results of Fig.2wefitted V(Q2,y c,r,s)by a linear function of s and definedW(Q2,y c,r)≡d V fit(Q2,y c,r,s)d s,(14)which,by construction,is s–independent function of Q2,y c and r.Positive W means that the variation ofΛin the PDF is more important than that in the hard scattering cross–sections,while for negative W the situation is opposite.The Q2–dependence of W(Q2,y c,r)is plotted in Fig.4a-c for three values of y c=0.01,0.02,0.04andfive values of r=0.1,0.2,0.3,0.4,0.5GeV.In Fig.5a we compare the Q2dependence of W(Q2,y c,r=0.2GeV)for different values of y c=0.01,0.02,0.04. Similar plots can be drawn for other values of r as well.From Figs.2–5a we conclude that at the NLO:•For Q2below40GeV2the sensitivity of(1)toΛcomes dominantly from PDF,while above 40GeV2the situation rapidly changes and most of this sensitivity comes from hard scattering cross–section.•Above Q2≈103GeV2the sensitivity toΛin PDF becomes negligible.•The preceding conclusions depend only weakly on y c.At the LO the general features are the same as those displayed in Figs.2–5a and we therefore merely summarize them in paring Figs.5a and5b we conclude that at the LO the relative importance of varyingΛpdf with respect toΛhsc is bigger than at the NLO.8Figure5:The Q2–dependence of W(Q2,y c,r=0.2)for three different values of y c at the NLO(a) and LO(b).All curves correspond to the case of no cuts.9Figure6:The same as in Fig.3but for the H1acceptance cuts.3.2H1cutsIn[1]only events satisfying certain acceptance cuts,most notably the cut on polar angle of outgoing jets in HERA laboratory frame,10◦≤θjet lab≤145◦,were selected for the analysis.In Fig.6 plots analogous to those of Fig.3,but incorporating these cuts,are displayed.We see that the experimental cuts affect mostly the low Q2region,where beside lowering the values of R2+1(Q2) they also strongly suppress the sensitivity of R2+1(Q2)to the variation ofΛin the PDF.This effect can be understood as follows.By imposing the mentioned angular cuts,one removes events with jets thatfly into a large part of the backward(with respect to the proton direction)lab frame hemisphere.We recall that in direct photon interactions(in contrast to the resolved ones),i.e. also DIS,a large fraction of jets populates the backward hemisphere in theγp CMS.Because the transverse boost between theγp CMS and HERA lab frame is proportional to Q2,the cut on the jet polar angle in the lab system is more effective for small Q2than for high Q2.Hence the drastic suppression of R2+1(Q2)at low and only moderate at high Q2.Furthermore,as low Q2means in average also small x,and most of the sensitivity of R2+1(Q2)toΛin PDF comes from the small x region,the H1cuts will significantly reduce it mainly for low Q2.On the basis of Fig.6we conclude that in the region Q2≥100GeV2,used in[1]for the extraction ofΛfrom the measured R2+1(Q2),the variation ofΛin the PDF could be neglected10with respect to the variation ofΛin the hard scattering cross–sections.4ConclusionsIn this paper we have constructed parameterizations of PDF corresponding to solutions of the evolution equations withfixed suitably defined boundary conditions and variableΛ.These pa-rameterization were then used to investigate,for the quantity R2+1,the numerical importance of varyingΛin PDF.We concluded that:•If no cuts are applied on produced jets the sensitivity of(1)to variation ofΛin PDF is bigger at the LO than at the NLO.•At moderate Q2,roughly below40GeV2,the sensitivity of(1)toαs comes dominantly from PDF,while at higher Q2the hard scattering cross–sections take rapidly over as the main source of theΛ–dependence of(1).•The preceding conclusions are only weakly dependent on y c.•Including the cuts applied by the H1Collaboration leads to strong suppression of the sensi-tivity toαs in the moderate Q2region.It is clear that a less restrictive treatment of the jets in the Q2region between,say,10and100 GeV2could provide much better possibility for a precise determination ofαs.This region is also very interesting from another point of view,and namely the question of the transition between the dynamics of deep inelastic scattering and photoproduction.The data in this region could bring new information on the structure of the virtual photon[16]and/or lead to new phenomena. AcknowledgmentsThis work had been supported in part by the grant No.201/96/1616of the Grant Agency of the Czech Republic.References[1]T.Ahmed et al.,H1Coll.:Phys.Lett.B346(1995)415.[2]M.Derrick et al.,ZEUS Coll.:Phys.Lett.B363201.[3]D.Graudenz:PROJET4.1MC generator,CERN-TH.7420/94.[4]E.Mirkes, D.Zeppenfeld:MEPJET MC generator,Phys.Lett.B380(1996)105,hep-ph/9511448[5]T.Brodkorb,E.Mirkes:DISJET MC generator:Z.Phys.C66(1995)141[6]D.Graudenz:Phys.Lett.B256(1991)518.[7]A.D.Martin,R.G.Roberts and W.J.Stirling:Phys.Rev.D47(1993)867.[8]J.Botts et al.,CTEQ Coll.:Phys.Lett.B304(1993)159.[9]M.Gl¨u ck,E.Reya,A.Vogt:Z.Phys.C67(1995)433.[10]J.Ch´y la,J.Rameˇs:PRA-HEP/96-01,hep-ph/960430611[11]H.D.Politzer:Nucl.Phys.B192(1982)493.[12]A.Buras:Rev.Mod.Phys.52(1980)199.[13]M.Gl¨u ck,E.Reya,A.Vogt:Z.Phys.C53(1992)127.[14]A.Vogt:Phys.Lett.B354(1995)145.[15]A.Martin,G.Roberts,W.J.Stirling:Phys.Lett.356(1995)89.[16]J.Ch´y la,J.Cvach:in Future Physics at Hera,ed.G.Ingelman,A.de Roeck,R.Klanner,Hamburg1996,p.54512。

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