Keokuk DMAIC Report Cameron Plate 4-600
可堪培拉公司产品说明书
CANBERRA CORPORATIONSAFETY DATA SHEET1. IdentificationProduct Identifier: HUSKY 1230 DISINFECTANT DEODORANTApplication or recommended use: Hard surface disinfectantRestrictions on use: Do not use in any fashion not specified on the product label.Manufacturer / supplier: Canberra Corporation3610 N. Holland-Sylvania Rd.Toledo, Ohio 43615 USATelephone: 419-841-6616Emergency phone: 866-836-88552. Hazards IdentificationGHS Classification: Classification of this mixture in accordance with paragraph (d) of §1910.1200.Flammable Aerosols - Category 1Eye Damage/Irritation - Category 2ALabel Elements:Symbol:Signal word: DANGERHazard statements: Extremely flammable aerosol. Causes serious eye irritation.Precautionary statements: Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Do not spray on an openflame or other ignition source. Pressurized container: Do not pierce or burn, even after use.Wash thoroughly after handling. Wear eye/face protection.IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if presentand easy to do. Continue rinsing. If eye irritation persists, get medical advice/attention.See 4. First-Aid Measures for specific treatment.Store locked up. Protect from sunlight. Do not expose to temperatures exceeding 50°C/122°F.Dispose of contents/container to an approved disposal facility.Other Hazards: None known.3. Composition / Information on IngredientsChemical characterization: Mixture of water, emulsifiers, solvents and auxiliary agents.Hazardous ingredients: The exact percentage of composition has been withheld as a trade secret.40 - 60% Ethyl Alcohol CAS 64-17-510 - 20% Butane CAS 106-97-82 - 10% Propane CAS 74-98-60.1 – 1% o-Phenylphenol CAS 90-43-74. First-aid measuresInhalation: Move to fresh air. Call a physician if symptoms develop or persist.Skin contact: Wash with plenty of soap and water. Get medical attention if irritation develops and persists.Eye contact: Immediately flush eyes with plenty of water for at least 15 minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists: Get medical advice/attention.Ingestion: In the unlikely event of swallowing contact a physician or poison control center. Rinse mouth thoroughly.Most important symptoms/effects, acute and delayed: Headache. Irritation of nose and throat. Severe eye irritation. Symptoms may include stinging, tearing, redness, swelling, and blurred vision. Coughing. Skin irritation.Indication of immediate medical attention and special treatment needed: Provide general supportive measures and treat symptomatically. Keep victim under observation. Symptoms may be delayed.5. Fire-fighting measuresSuitable extinguishing media: Alcohol resistant foam. Water spray. Water fog. Dry chemical. Carbon dioxide (CO2). Unsuitable extinguishing media: Do not use water jet as an extinguisher, as this will spread the fire.Specific hazards arising from the chemical: Contents under pressure. Pressurized container may explode when exposed to heat or flame. During fire, gases hazardous to health may be formed.Special protective equipment and precautions for firefighters: Self-contained breathing apparatus and full protective clothing must be worn in case of fire.Fire-fighting equipment/instructions: Move containers from fire area if you can do so without risk. Cool containers exposed to heat with water spray and remove container, if no risk is involved. Containers should be cooled with water to prevent vapor pressure build up.General fire hazards: Extremely flammable aerosol.6. Accidental release measuresPersonal precautions, protective equipment and emergency procedures: Keep unnecessary personnel away. Keep people away from and upwind of spill/leak. Keep out of low areas. Eliminate all ignition sources (no smoking, flares, sparks, or flames in immediate area). Wear appropriate protective equipment and clothing during clean-up. Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Ventilate closed spaces before entering them. Local authorities should be advised if significant spillages cannot be contained.Methods and materials for containment and cleaning up: Eliminate all ignition sources (no smoking, flares, sparks, or flames in immediate area). Keep combustibles (wood, paper, oil, etc.) away from spilled material. Stop leak if you can do so without risk. Move the cylinder to a safe and open area if the leak is irreparable. Cover with plastic sheet to prevent spreading. Absorb in vermiculite, dry sand or earth and place into containers. Scoop up used absorbent into drums or other appropriate container. Prevent entry into waterways, sewer, basements or confined areas. Following product recovery, flush area with water. Small Spills: Wipe up with absorbent material. Clean surface thoroughly to remove residual contamination. Environmental precautions: Avoid release to the environment. Avoid discharge into drains, water courses or onto the ground.7. Handling and storagePrecautions for safe handling: Pressurized container: Do not pierce or burn, even after use. Do not use if spray button is missing or defective. Do not spray on a naked flame or any other incandescent material. Do not smoke while using or until sprayed surface is thoroughly dry. Do not cut, weld, solder, drill, grind, or expose containers to heat, flame, sparks, or other sources of ignition. All equipment used when handling the product must be grounded. Do not handle or store near an open flame, heat or other sources of ignition. Avoid contact with eyes. Use only in well-ventilated areas. Wear appropriate personal protective equipment. Avoid release to the environment. Observe good industrial hygiene practices.Conditions for safe storage, including any incompatibilities: Level 2 Aerosol.Pressurized container. Protect from sunlight and do not expose to temperatures exceeding 50°C/122 °F. Do not puncture, incinerate or crush. This material can accumulate static charge which may cause spark and become an ignition source. Do not handle or store near an open flame, heat or other sources of ignition. Store in original tightly closed container. Store away from incompatible materials.8. Exposure controls/personal protectionOccupational exposure limitsUS. OSHA Table Z-1 Limits for Air Contaminants (29 CFR 1910.1000)Components Type ValueEthyl Alcohol (CAS 64-17-5) PEL 1900 mg/m3 (1000 ppm)Propane (CAS 74-98-6) PEL 1800 mg/m3 (1000 ppm)US. ACGIH Threshold Limit ValuesComponents Type ValueButane (CAS 106-97-8) STEL 1000 ppmEthyl Alcohol (CAS 64-17-5) STEL 1000 ppmUS. NIOSH: Pocket Guide to Chemical HazardsComponents Type ValueButane (CAS 106-97-8) TWA 1900 mg/m3 (800 ppm)Ethyl Alcohol (CAS 64-17-5) TWA 1900 mg/m3 (1000 ppm)Propane (CAS 74-98-6) TWA 1800 mg/m3 (1000 ppm)Appropriate engineering controls: Good general ventilation should be used. Ventilation rates should be matched to conditions. If applicable, use process enclosures, local exhaust ventilation, or other engineering controls to maintain airborne levels below recommended exposure limits. If exposure limits have not been established, maintain airborne levels to an acceptable level. Provide eyewash station.Individual protection measures, such as personal protective equipment:Eye/face protection: Wear safety glasses with side shields (or goggles).Hand protection: Wear appropriate chemical resistant gloves.Other: Wear suitable protective clothing.Respiratory protection: If permissible levels are exceeded use organic vapor cartridge or an air-supplied respirator.General hygiene considerations: When using do not smoke. Always observe good personal hygiene measures, such as washing after handling the material and before eating, drinking, and/or smoking. Routinely wash work clothing and protective equipment to remove contaminants.9. Physical and chemical propertiesAppearancePhysical state: Gas. Form: Aerosol.Color: Not available. Odor: Not available.Odor threshold: Not available. pH: Not available.Melting point/freezing point: Not available. Flash point: -156.0 °F (-104.4 °C) Propellant estimated.Evaporation rate: Not available. Initial boiling point/boiling range: 140.71 °F (60.39 °C) estimated. Flammability: Not available. Auto-ignition temperature: 856.4 °F (458 °C) estimated.Upper/lower flammability or explosive limitsFlammability limit – lower (%): 2.6 % estimated. Flammability limit – upper (%): 12.8 % estimated.Explosive limit - lower (%): Not available. Explosive limit - upper (%): Not available.Vapor pressure: 75 - 85 psig @70F estimated. Vapor density: Not available.Relative density: Not available. Specific gravity: 0.79 estimated.Solubility (water): Not available. Viscosity: Not available.Decomposition temperature: Not available.Partition coefficient (n-octanol/water): Not available.10. Stability and reactivityReactivity: The product is stable and non-reactive under normal conditions of use, storage and transport.Chemical stability: Material is stable under normal conditions.Possibility of hazardous reactions: Hazardous polymerization does not occur.Conditions to avoid: Avoid temperatures exceeding the flash point. Contact with incompatible materials.Incompatible materials: Strong oxidizing agents. Nitrates. Fluorine. Chlorine.Hazardous decomposition products: No hazardous decomposition products are known.11. Toxicological informationInformation on likely routes of exposure:Ingestion: Expected to be a low ingestion hazard.Inhalation: No adverse effects due to inhalation are expected.Skin contact: No adverse effects due to skin contact are expected.Eye contact: Causes serious eye irritation.Symptoms related to the physical, chemical and toxicological characteristics: Headache. Irritation of nose and throat. Severe eye irritation. Symptoms may include stinging, tearing, redness, swelling, and blurred vision. Coughing. Skin irritation. Information on toxicological effects:Acute toxicity: Expected to be a low hazard for usual industrial or commercial handling by trained personnel.Skin corrosion/irritation: Prolonged skin contact may cause temporary irritation.Serious eye damage/eye irritation: Causes serious eye irritation.Respiratory sensitization: Not available. Skin sensitization: This product is not expected to cause skin sensitization. Carcinogenicity: This product is not considered to be a carcinogen by IARC, ACGIH, NTP, or OSHA.IARC Monographs. Overall Evaluation of Carcinogenicity: o-Phenylphenol (CAS 90-43-7) 3 Not classifiable as to carcinogenicity to humans.OSHA Specifically Regulated Substances (29 CFR 1910.1001-1050): Not listed.Reproductive toxicity: This product is not expected to cause reproductive or developmental effects.Specific target organ toxicity - single exposure: Not classified.Specific target organ toxicity - repeated exposure: Not classified.Aspiration hazard: Not available.Chronic effects: Prolonged or repeated contact may cause drying, cracking, or irritation.12. Ecological informationEcotoxicity: Harmful to aquatic life with long lasting effects.Persistence and degradability: No data is available on the degradability of this product.Bioaccumulative potential: No data available.Partition coefficient n-octanol / water (log Kow): Butane 2.89, Ethyl Alcohol -0.31, o-Phenylphenol 3.09, Propane 2.36 Mobility in soil: No data available.Other adverse effects: No other adverse environmental effects (e.g. ozone depletion, photochemical ozone creation potential, endocrine disruption, global warming potential) are expected from this component.13. Disposal considerationsDisposal instructions Collect and reclaim or dispose in sealed containers at licensed waste disposal site. Contents under pressure. Do not puncture, incinerate or crush. Do not allow this material to drain into sewers/water supplies. Do not contaminate ponds, waterways or ditches with chemical or used container. Dispose of contents/container in accordance with local/regional/national/international regulations.Waste from residues / unused products: Dispose of in accordance with local regulations. Empty containers or liners mayretain some product residues. This material and its container must be disposed of in a safe manner.Contaminated packaging: Empty containers should be taken to an approved waste site for recycling or disposal. Emptiedcontainers may retain product residue, follow label warnings even after container is emptied.14. Transport informationDOT UN number UN1950 UN proper shipping name Aerosols, flammable Class 2.1Packing group: Not applicable.Read safety instructions, SDS and emergency procedures before handling.Packaging exceptions: This product meets the exception requirements of section 173.306 as a limited quantity andmay be shipped as a limited quantity.15. Regulatory informationUS federal regulationsFIFRA: This product is a U.S. EPA Registered pesticide, EPA Reg. No. 706-69-8155, and is subject to certain labelingrequirements under Federal pesticide law. These requirements differ from the classification criteria and hazard informationrequired for safety data sheets (SDS), and for workplace labels of non-pesticide products.This product is a "Hazardous Chemical" as defined by the OSHA Hazard Communication Standard, 29 CFR 1910.1200.All components are on the U.S. EPA TSCA Inventory List.TSCA Section 12(b) Export Notification (40 CFR 707, Subpt. D): Not regulated.CERCLA Hazardous Substance List (40 CFR 302.4): Sodium Nitrite (CAS 7632-00-0) Listed.SARA 304 Emergency release notification: Not regulated.OSHA Specifically Regulated Substances (29 CFR 1910.1001-1050): Not listed.Superfund Amendments and Reauthorization Act of 1986 (SARA):Hazard categoriesImmediate Hazard – Yes Delayed Hazard – NoFire Hazard – Yes Pressure Hazard – NoReactivity Hazard – NoSARA 302 Extremely hazardous substance: NoSARA 311/312 Hazardous chemical: NoSARA 313 (TRI reporting)Chemical name CAS number % by wt.o-Phenylphenol 90-43-7 0.1 - 1Other federal regulationsClean Air Act (CAA) Section 112 Hazardous Air Pollutants (HAPs) List: Not regulated.Clean Air Act (CAA) Section 112(r) Accidental Release Prevention (40 CFR 68.130):Butane (CAS 106-97-8) Propane (CAS 74-98-6)Safe Drinking Water Act: (SDWA): Not regulated.US state regulationsUS. Massachusetts RTK - Substance ListUS. New Jersey Worker and Community Right-to-Know ActUS. Pennsylvania Worker and Community Right-to-Know LawButane (CAS 106-97-8) Ethyl Alcohol (CAS 64-17-5) o-Phenylphenol (CAS 90-43-7) Propane (CAS 74-98-6)US. Rhode Island RTKButane (CAS 106-97-8) o-Phenylphenol (CAS 90-43-7) Propane (CAS 74-98-6)US. California Proposition 65: WARNING: This product contains a chemical known to the State of California to causecancer. o-Phenylphenol (CAS 90-43-7) Listed: August 4, 200016. Other information, including date of preparation or last revisionDate issued: 01. 02. 2015 HSK-1230 Revision: N/ADisclaimer The information provided in this Safety Data Sheet is correct to the best of our knowledge, information and beliefat the date of its publication. The information given is designed only as a guidance for safe handling, use, processing, storage, transportation, disposal and release and is not to be considered a warranty or quality specification. The information relates onlyto the specific material designated and may not be valid for such material used in combination with any other materials or inany process, unless specified in the text. We cannot anticipate all conditions under which this information and its product, orthe products of other manufacturers in combination with its product, may be used. It is th conditions for handling, storage and disposal of the product, and to assume liability for loss, injury, damage or expense due toimproper use. The information in the sheet was written based on the best knowledge and experience currently available.。
Klauke EK50ML Battery Powered Cable Crimping Tool
Manuals+— User Manuals Simplified.Klauke EK50ML Battery Powered Cable Crimping Tool InstructionsHome » Klauke » Klauke EK50ML Battery Powered Cable Crimping Tool InstructionsContents1 Klauke EK50ML Battery Powered Cable CrimpingTool2 Product Information3 Product Usage Instructions4 Product Parts5 Dimension6 How To Use?7 Spare parts8 Documents / Resources8.1 References9 Related PostsKlauke EK50ML Battery Powered Cable Crimping ToolDimensionHow To Use?might results in destroying the battery by deep discharge!GBWeight (incl. battery):~ 0,96 kg Battery capacity 2,5 Ah, Li-Ion (RA ML1225)Crimping force:15 kN (max.)Charging time:40 min. (RAML1)Environmental temp.:-10°C – +40°C Battery voltage:10,8 V Crimping time:< 1,5 s (depending on the connector size)Crimp per battery~400 crimps (10 mm² Cu DIN 46234)Sound level< 70 dB (A) in 1m distanceVibrations:< 2,5 m/s²Spare partsEK50ML (with AE5071, AE5072, AE5073 and ZAE5072 dies)press image squaresize ferrules Number of crimps 0,51690, 1690K, 1690H, GR170W, 4698, GR4696, 4696, GR4708, ST970810,751708, 1706, GR1738, 170W, 170WK, 170WH, 170WL, GR171G,4708, GR4706, 4706, 47012, GR4718, ST971811171G, 171GK, 171GH, 171GL, GR172RO,4718, 4716, 47110, 47112, GR4728, ST972811,5172RO, 172RK, 172RH, 172RM, 172RL, 175S, 4728, GR4726, 4726,4728, GR4726, 4726, 47212, 47218, GR4738, ST9738, 43210, 43381 – 22,51738, 17312, 17318, 17410, 4738, 47318, 47310, 47410, 43312, 43410 1 – 2 417412, 17418, 17512, 47412, 47418, 47512, 43512 1 – 2 617518, 17612, 175SL, 176E, 47518, 47612, 43612 1 – 2 1017618, 17712, 176EL, 178BR, 47618, 47712, 43712 1 – 2 1617712, 17718, 47712, GR47712, 47718, 43712 1 – 2 2517816, 17818, 17822, 178BR, 178BRL, 47816, 47818, 47822235179B, 179BL, 47916, 47918, 479252501800, 1800L, 48020, 4802522 x 68751412 x 108761412 x 16877141CE-´* – Declaration of conformity. We declare under our sole responsibility that this product is in conformity with the following standards or normative documents: EN 62841-1, EN ISO 12100, EN ISO 13857, EN ISO 13854,EN 28662-1, EN 61000-6-3, EN 61000-6-2, EN 60529, EN ISO 14118 in accordance with the regulations of directives2006/42/EG, 2014/30/EU, 2011/65/EUUKCA-´* – Declaration of conformity. We declare under our sole responsibility that this product is in conformity with the following standards or normative documents: BS EN 62841-1, BS EN ISO 12100,BS EN ISO 13857, BS EN ISO 13854, BS EN 28662-1, BS EN 61000-6-3, BS EN 61000-6-2, BS EN ISO 14118 inaccordance with the regulations of directives 2006/42/EG, 2014/30/EU, 2011/65/EUDocuments / ResourcesKlauke EK50ML Battery Powered Cable Crimping Tool [pdf] InstructionsEK50ML, EKWF50ML, EC50ML, EK50ML Battery Powered Cable Crimping Tool, Battery Powered Cable Crimping Tool, Powered Cable Crimping Tool, Cable Crimping Tool, Crimping Tool ReferencesVerbindungen mit System | KlaukeManuals+,。
Non-InvasiveandInvasiveCardiacImagingIntroduction
Non-Invasive and Invasive Cardiac ImagingIntroduction:Coronary artery disease is the most common cause of patient hospitalization and mortality in many industrialized countries. The current standard of assessment is coronary angiography (CA) in conjunction with interventional therapeutic procedures. While CA and other invasive cardiac imaging procedures have become relatively safe, the inconvenience to the patient is extensive. This has caused a popularization throughout the past decades of potential, non-invasive cardiac imaging devices. Different devices such as magnetic resonance and electron beam computed tomography have been explored. In this monograph various imaging technologies are discussed.The Problem:The current cardiac imaging devices provide an inconvenience to the patient in many forms including hospitalization and higher economic burden. Various technologies have been developed to ease patient burden in the form of non-invasive cardiac imaging devices. However, these new technologies are not without their unique challenges. Such challenges as cardiac motion and calcium deposits often render scans inadequate. The characterization of atherosclerotic plaque is another major challenge for non-invasive imaging as the rupture of such plaques can cause acute vessel occlusion. There is a need to find a suitable procedure that minimizes or eliminates rupturing the plaque. In addition, conventional imaging techniques expose the patient to ionizing radiation. These are some of the various challenges surrounding the design of a non-invasive device.Invasive ImagingModern IVUS systems have presented some difficulties that necessitate further exploration. One such difficulty with IVUS is total obstruction when a transducer is brought in close proximity to a severely stenosed vessel. Volcano Corporation recently launched the VH ™ IVUS system. This is the first technology to enable real-time compositional assessment of atherosclerotic plaque in coronary arteries. It provides automated measurement tools to simplify image interpretation. It also uses a color key to better display plaque composition. This technology allows for colorized VH images of four plaque component types. This is the first IVUS system capable of providing information about plaque composition.Optical Coherence Tomography (OCT) is another popular technology used for cardiac imaging. This non-contact, light-based imaging modality providesin situ tissue images at near histological resolution. This technique allows for the identification of mural as well as luminal morphologies. When comparedto IVUS, studies showed that OCT provides additional morphologic information which is helpful in the characterization of plaque. Optical frequencydomain imaging (OFDI) is a new technology in this area of imaging. OFDI is used in the diagnosis and management of coronary artery disease. It uses infrared light delivered to the imaging site through a single optical fiber incorporated within a catheter. Advanced algorithms are used to remove thereflected signals from the infrared light. This provides the clinician with real-time cross sectional and 3-dimensional images.Non-invasive Imaging:Nuclear cardiac imaging is a popular non-invasive imaging method which uses technetium Tc 99m sestamibi (MIBI), a radionuclide, in its process. MIBI is a technetium imaging agent that is used to reveal blood-starved tissue, usually during a heart attack. It has been used for more than a decade as an imaging agent. MIBI concentrates in tissues in proportion to desmoplastic and metabolic activity and blood flow. This technique has been considered a reliable method of assessing myocardial salvage in patients with acute myocardial infarction in addition to evaluating and diagnosing a heart attack.(Nuclear cardiac illustration from Google Images)Cardiovascular Magnetic Resonance (CMR) is another technique used for non-invasive imaging. This device was developed to quantify calcium deposits and coronary morphology and flow. It is based upon the magnetic characteristics of tissues and molecules within a magnetic field. CMR is superior to other methods for use on those patients with complex congenital heart disease. CMR provides excellent visualization of extracardiac venous structures and intracardiac baffles as well. However, it is not feasible for use on patients with pacemakers or other metallic implants or on those who suffer from claustrophobia.Most recently, the technique of spiral balanced steady-state free precession cardiac imaging (SSFP) has been brought to the forefront of CMR. These sequences are useful in cardiac imaging because they have the ability to achieve high signal efficiency and blood-myocardium contrast. This procedure enables efficient acquisition with reduced blood flow and motion artifacts. SSPF has been combined with spiral imaging allowing for real-time interactive cardiac CMR. In contrast to conventional echo imaging, this method yields an intrinsic blood-myocardium contrast independent of inflow and has become extremely useful in cardiac imaging.Computed Tomography (CT) is another well-known device that is being used for non-invasive cardiac imaging. Like CMR, electron beam computed tomography (EBCT) was designed with the goal of measuring calcium deposits and coronary artery morphology and flow. CT of the heart throughout the last decade has been the exclusive realm of EBCT. The most popular use for this technology has been assessment of myocardial perfusion and function as well visualization of the coronary arteries.In recent years, multidetector-row computed tomography (MDCT) has become available. This technology has become the preferred method because it rectifies some of the limitations of the EBCT such as low special resolution and pronounced noise. The ability of the MDCT scanners to acquisition multiple slices has considerably improved cardiac imaging. The image quality produced by MDCT favorably compares to that of coronary angiography. In addition, it provides assessment of coronary calcium and plaque characterization while also producing a high image quality.Non-invasive echocardiography is an optional ultrasonic method of cardiac imaging. Recently, live three dimensional echocardiography (L3DE) has broken though into the field of medical ultrasound. This non-invasive system is easy to operate and images rapidly and clearly. In L3DE ultrasonic beams are generated in a phased array manner which gives the clinician the ability to evaluate the cardiac structures from every direction. The ability of the operator to improve temporal and special resolution of the image during acquisition is one benefit of this procedure.References and Bibliography:World Wide Web•http://www.mediguide.co.il/MediGuide-Medical Positioning System•Health Center Laboratories•Echocardiography (Ultrasound of the Heart)•Cardiac Perfusion Scan•Technetium tc 99m sestamibi-definition from •Google Images•/cgi/news/release?id=146453Press Release: Volcano Corp. Announces Commercial Release of VH™ IVUS SystemJournal articles and Reviews•_________. Terumo Initiates Vulnerable Plaque Program with Exclusive License from Massachusetts General Hospital. Press Release December 15, 2004.•Coover LR. The Role of Technetium Tc 99m Sestamibi in the Early Detection of Breast Carcinoma. Hospital Physician 1999: 16-21.•Dong J, Ndrepepa G, Schmitt C, et. al. Early Resolution of ST-Segment Elevation Correlates With Myocardial Salvage Assessed by Tc-99m Sestamibi Scintigraphy in Patients With Acute Myocardial Infarction After Mechanical or Thrombolytic Reperfusion Therapy. Circulation 2002,105: 2946-2949.•Gaudio C, Mirabelli F, Di Michele S, et. al. Multidetector Computed Tomography of the Coronary Arteries. Ital Heart J 2004, 5: 423-430.•Gerckens U, Buellesfeld L, McNamara E, Grube E. Optical Coherence Tomography (OCT): Potential of a new high-resolution intracoronary imaging technique. Herz 2003, 28(6): 496-500.•Kiaffas MG, Davlourous P, Tsertos F, et. al. Cardiovascular Magnetic Resonance Evaluation of Patients with Transposition of the Great Arteries Following Atrial Switch Surgical Correction 2005, 46: 69-73.•Light ED and Smith SW. Two Dimensional Arrays for Real Time 3D Intravascular Ultrasound 2004, 26(2): 115-128.•Nayak KS, Hargreaves BA, HU SB, et. al. Spiral Balanced Steady-State Free Precession Cardiac Imaging. Magnetic Resonance Medicine 2005, 53: 1468-1473.•Nieman K, van Genus RM, Wieloposki, P, et. al. Noninvasive Coronary Imaging: A comparison of computed tomography and magnetic resonance techniques. Reviews in Cardiovascular Medicine 2002, 3(2): 77-84.•Wang XF, Deng YB, Nanda NC, et. al. Live Three-Dimensional Echocardiography: Imaging principles and clinical application.Echocardiography: A journal of CV Ultrasound & Allied Technologies 2003, 20(7): 593-604.。
法国科玛嘉蜡样芽孢杆菌显色培养基说明书
法国科玛嘉蜡样芽孢杆菌显色培养基使用说明书
此显色培养基用于分离和鉴别蜡样芽孢杆菌。
一、组成
科玛嘉蜡样芽孢杆菌基础培养基和增补剂各一瓶。
基础干粉贮存于15-30℃环境中，增补剂贮存于2-8℃环境中。
二、成分（g/L）
琼脂：15.0 蛋白胨和酵母浸出物8.0 NaCl 5.0 色素8.2
pH：6.8±0.2
三、操作：
⊙基础干粉
取瓶内基础干粉加入1000ml蒸馏水中（可根据需要按照33.2g/L的比例扩大或缩小），搅拌至琼脂溶解。
常规高压灭菌（121℃,15min），然后水浴冷却至47±2℃。
⊙增补剂
取增补剂一瓶加入40ml无菌水中（可根据需要按照3g/L的比例扩大或缩小），用磁力搅拌器快速搅拌（-1200rpm）均匀（时间不少于30分钟），使其完全溶解，最终成为奶油状的匀质溶液。
常规高压灭菌（121℃,15min），然后水浴冷却至47±2℃。
把混匀后的增补剂加入到冷却好的基础培养基中，轻轻混匀，然后倾入无菌培养皿中，使其凝固。
此成品平板可在室温保存一天；在冰箱里可保存两周（2-8℃，避光、干燥）。
三、结果
初筛微生物菌落外观
蜡样芽孢杆菌蓝色，带白色晕环
其他微生物蓝色、无色或被抑制
★使用过的培养基需要在121℃灭菌至少20分钟才可以按照有关规定丢弃。
科赛勒产品中英文对照表
赛默飞世尔科学 Cytomat
Thermo ScientificCytomat®Automated Incubatorsand Storage ModulesThe only incubator and storagesystems that combine provenreliability and environmentalstability with worldwide support.Our Cytomat support increases yourproductivity via higher uptime,reduced costs, and optimizedsystems performance.Thermo ScientificCytomat 6000Automatic Incubators Thermo ScientificCytomat 44Automated PlateStorage ModuleAccessing the Industry’s Most Intensive SupportThermo Scientific Cytomat service and support are backed up by the global network of ThermoFisher Scientific, the world leader in serving science. Like all of our services, Cytomat supporthelps increase your productivity via higher uptime, reduced costs, and optimized systemsperformance.If Cytomat’s standard solutions don’t fit your requirements, our Engineering and R&D teams candesign and develop customized products that meet the most demanding needs. Our in-housemechanical, software, and application experts work closely with our production and develop-ment facility to offer assistance around the globe. Whatever your concern, you get fast,dedicated local support virtually anywhere.Software IntegrationOur experts will help your system operate seamlessly with any automated assay solution. We minimize and simplify robotic teaching and programming for fast imple-mentation and start-up. Software commands are easy and intuitive. And Cytomat’s single loading and unloading point cuts down on robotic programming time and effort.Customized SolutionsDefine the configuration ofyour robotic system or work-station through a choice ofmicroplate, T-flask, or Petri-dish handling, temperature,and humidity ranges, and gasenvironment options to pro-vide the right atmosphere fordifferent screening or samplestorage applications.Whatever your Cytomat sys-tem configuration, we providefull documentation and certi-fication of quality. As aservice, we also offer IQ, OQvalidation.Field ServiceIn addition to phone oremail-based technical help,you can access experiencedfield service specialists dedi-cated to Cytomat systems.More than 100 trained serviceengineers are available tominimize mean time to repair.Thermo Scientific Cytomat Linear HotelThermo Scientific Cytomat 600X System StackedThermo Scientific Cytomat HotelReaping the Benefits of Proven ReliabilityWhen valuable assay samples are properly stored and accessed, research laboratories can achieve significant strides in productivity and efficiency.That’s why laboratory equipment manufacturers andresearchers worldwide depend on highly reliable Thermo Scientific Cytomat automated incubators and microplate storage systems. The robot-accessible Cytomat line is the established leader in the field:•Provides continuous operation and maximum sample protection •Incorporates more than 40 years’ experience in CO 2incubator technology •Offers the industry’s broadest and deepest range of automated incubators and storage modules •Integrates seamlessly with all automated assay systems •Furnishes superior conditions for automated cell-based assays, cell cultures, bacterial assays, microarraying,compound libraries, and other applications requiring precise environmental control •CE & CSA approval•Operates laboratory for calibration of temperature according to EN ISO/IEC 17025 (DKD certification)Relying On Trusted Environmental ExpertiseThe Cytomat system accommodates all standard microplate formats, and provides a choice of temperature (–20°C to 70°C)and humidity ranges, as well as gaseous atmospheres.Cytomat incubators create ideal environmental conditions for cell-based assays. Cooled storage systems ensure an extremely dry climate with an inert atmosphere, minimizing DMSO water absorption. By contrast, primer hybridization systems create hot and humid conditions to minimize evaporation.Both types emphasize reliable, stable environmental condi-tions for microplates. Results: reduced assay variance,excellent parameter uniformity, and virtual elimination of recovery times.Superior Cytomat design and manufacturing quality provide incubation and storage with ISO 9001 quality certification.Thermo Scientific Cytomat ®Automated Incubators and Storage ModulesProgressive Plate Shuttle SystemUnique Swap StationWireless Barcode ReaderStackerTaking Advantage of Our Innovative DesignWith Cytomat, users get the industry’s most advanced technology for automated storage and retrieval within a precisely controlled environment.Our internally automated Thermo Scientific Plate Shuttle ™system opti-mizes microplate handling. It comprises a lift system, a handler for X/Y/Z movement axes, and a heated automatic access door. Plate access won’t disturb inner chamber conditions. Integration is a snap with any automated assay system.Capacity can reach from 40 to 1,008 shal-low-well plates (capacity can vary depending on plate type). Random access of individual plates optimizes workflow.And easy-to-use, Windows ®-based software allows onsite system reconfiguration and testing.Ease of IntegrationThe Cytomat system delivers itsmicroplates to a single point of integra-tion — a transfer station, normally configured for portrait format — during unloading. It retrieves plates from the same point during loading.This creates an extremely robot-friendly design. On system implementation, the robot needs to be taught only one position for plate pickup. You save significant time during both installation and minute-to-minute operation.Choosing the Right OptionsT ransfer StationsThe highly flexible Cytomat offers a variety of ways to present plates to the system.The standard Cytomat configuration fea-tures rear presentation. For top-of-counter presentation, a lifter is available. Other choices include 90°turning for presenta-tion in landscape format, a 180°turntable Swap Station with two positions, and a Linear Transfer Station.StackersThe ultra-flexible Thermo ScientificCytomat Stacker System accommodates all standard microplate formats (includ-ing deepwell plates) as well as tip boxes.Stackers are easily removed for manual loading and unloading, and can be auto-claved and sterilized with dry heat at 180°C.ShakerAn orbital shaking option is ideal for applications requiring sample agitation,such as insect cell growth and gene expression. The software makes it easy to control the shaking commands and parameters.Wireless Barcode ReaderAll Cytomat models are available with a robotically controlled, wireless barcode reader that can scan barcodes at any plate position — inside and outside the controlled environment. This highly flexi-ble inventory scanning capability allows information retrieval at any position,even when plates are manually loaded.This highly desirable feature minimizes plate movement and eliminates the process inefficiencies of fixed barcode scanners. With the wireless reader,Cytomat can provide data sets for sam-ple and plate tracking, functioning as both databank and compound store.~~-80 -20 -101020 30 40 50 60 70437T A (ambient)Temperature [°C]421895049241008984Standard MicroplatesCytomat 2C4Cytomat 2C70Cytomat 2C425Cytomat 2C450Cytomat 2C470Cytomat 6002D Cytomat 6003DCytomat 6000Cytomat 6001Cytomat 6001 C4Cytomat 6070Cytomat 2Hotel (ambient)Cytomat 6004 (ambient)Cytomat 24 CCytomat 24 C10Cytomat 24 C4Cytomat Hotel (ambient)Cytomat 24 Hotel (ambient)Cytomat 24 Linear Hotel (ambient)Cytomat 48 Linear Hotel (ambient)BioBankCytomat 44D/HC/HCytomat 48 CCytomat 48 C10Cytomat 48 C4Cytomat 2CCytomat 2C15CAPACITYSTORAGEINCUBATION HYBRIDIZATIONSelecting theRight Solutionfor Your AssayChoose from a wide range of Cytomat modelsto match your laboratory mission and desired environmental conditions. It’s easy to find pre-cisely the right Cytomat, whatever your requirements.Thermo Scientific ServicesWe are committed to helping your laboratory achieve success.Our solutions ensure that your automation systems are optimizedfor accuracy, productivity, and performance. We offer flexiblesolutions:•Service agreements•Preventative maintenance plans•Software upgrades•Software application support•Technical support•Integration services•Relocation services•TrainingContact a Thermo Fisher Scientific representative to tailor theservice solution that best meets your needs.Email:***********************************+49 6184 906940Email:**************************************+852 2885 4613Email:****************************************/automate0717030。
Thermo Scientific
DATA SHEET 2D Labtainer BioProcess Containers2D Labtainer BioProcess Container (BPC) systemsWhether in standard or customized configurations, Labtainer BPCs are ideal for:• Dispensing, packaging, and storing cell culture media, buffers, and process liquids• Delivery of cell culture media or process liquids to small-scale bioprocess systems• Bioreactor and fermentation feed, sampling, and harvest • Chromatography feed and fraction collection• Storage and transport of bulk intermediate products, process intermediates, vaccine conjugates, and other biological productsSmall-volume liquid handling systems for cell culture and bioprocessingThermo Scientific ™ Labtainer ™ BioProcess Containers (BPCs) effectively address small-volume liquid handling needs. They range in size from 50 mL to 50 L, with avariety of standard configurations to meet most application needs. These Labtainer BPCs are space efficient, ergonomic, and constructed of Thermo Scientific ™Aegis ™ 5-14 and CX5-14 films. Product configurations cover a range of industry-standard connection systems, and handling systems are available for transport and storage.Standard productsStandard Labtainer BPCs are stocked for immediate delivery and are fully supported by our process and product validation program. For more information on our validation program, please refer to our validation guides for Aegis5-14 and CX5-14 films. Additionally, standard Labtainer BPCs have validated liquid shipping configurations.Standard configurations can be customized for optimal fit, form, and function to address process-specific applications using one of the industry’s largest libraries of qualified components.2D Labtainer BPCs are available with the Thermo Scientific ™ BioTitan ™ Retention Device. This universaltubing retention solution was designed to provide the best method for retaining flexible tubing on a barbed fitting and helps eliminate the risk of leaks and failure of the tubingconnection point.Table 1. Chamber information.50 mL–2 L, 2-port Labtainer BPC 2 L–50 L, 3-port Labtainer BPC2 L–50 L: Polyethylene ports are welded into the BPC seam: one 1/4 in. ID and two 3/8 in. ID ports on standard chamber.Table 2. Custom BPC options.Tubing type C-Flex™ (animal origin–free), silicone, PharMed™, or AdvantaFlex™Tubing size Specific lengths of 3.18–25.4 mm ID (1/8–1 in.); specific length depends on type of tubing chosenConnectors • Luer: 3.18–6.35 mm (1/8–1/4 in.) ID• CPC quick-connect: 6.35–19 mm (1/4–3/4 in.) ID• Steam-in-place connector: 6.35–19 mm (1/4–3/4 in.) ID• Tri-clamp: 3.18–25.4 mm (1/8–1 in.) ID• Mini tri-clamp: 3.18–12.7 mm (1/8–1/2 in.) ID• Aseptic connection and aseptic disconnection devices: all available sizes of Colder AseptiQuik™, Pall™ Kleenpak™, Cytiva ReadyMate™ DACOthers • Needle-free sample port (SmartSite™ or Clave™ products)• Filter capsule (Millipore™, Pall™, Sartorius™, Parker Bioscience™, Meissner™ products)Table 3. Presentation (as dry BPC systems).Outer packaging Supplied “flat-packed”—two polyethylene outer layersLabel • Description• Product code• Lot number• Expiration date on outer packaging and shipping containerSterilization Irradiation (25–40 kGy) inner side of outer packaging Shipping container Durable cardboard cartonDocumentation • Certificate of Analysis provided with each batch for each delivery • Certificate of Irradiation2 portsPack of 10Line 1Luer lock body connection, polypropyleneTubing: C-Flex; 30 cm (12 in.) lengthID x OD: 3.18 x 6.35 mm (0.125 x 0.25 in.)Line 2Luer lock insert connection, polypropyleneTubing: C-Flex; 30 cm (12 in.) lengthID x OD: 3.18 x 6.35 mm (0.125 x 0.25 in.) Line 1Luer lock body connection, polypropyleneTubing: C-Flex; 8 cm (3 in.) lengthID x OD: 6.35 x 10.92 mm (0.25 x 0.43 in.)Line 2Luer lock insert connection, polypropyleneTubing: C-Flex; 8 cm (3 in.) lengthID x OD: 6.35 x 10.92 mm (0.25 x 0.43 in.)Line 1Luer lock body connection, polypropyleneTubing: C-Flex; 30 cm (12 in.) lengthID x OD: 3.18 x 6.35 mm (0.125 x 0.25 in.)Line 2MPC insert, polycarbonateTubing: C-Flex; 8 cm (3 in.) lengthID x OD: 3.18 x 6.35 mm (0.125 x 0.25 in.)2 portsPack of 10Pack of 10Line 1Luer lock insert connection, polypropyleneTubing: C-Flex; 30 cm (12 in.) length ID x OD: 6.35 x 9.7 mm (0.25 x 0.38 in.)Line 2Luer lock body connection, polypropylene Tubing: C-Flex; 30 cm (12 in.) length ID x OD: 6.35 x 9.7 mm (0.25 x 0.38 in.)Line 3Luer lock body connection, polypropylene Tubing: C-Flex; 30 cm (12 in.) lengthID x OD: 3.18 x 6.35 mm (0.125 x 0.25 in.)Line 1MPC insert, polycarbonateTubing: C-Flex; 61 cm (24 in.) length ID x OD: 9.7 x 15.9 mm (0.38 x 0.63 in.)Line 2MPC body, polycarbonateTubing: C-Flex; 61 cm (24 in.) length ID x OD: 9.7 x 15.9 mm (0.38 x 0.63 in.)Line 3Luer lock body connection, polypropylene Tubing: C-Flex; 61 cm (24 in.) length ID x OD: 3.18 x 6.35 mm (0.125 x 0.25 in.)Line 1MPC insert, polycarbonateTubing: C-Flex; 30 cm (12 in.) length ID x OD: 9.7 x 12.7 mm (0.38 x 0.5 in.)Line 2MPC insert, polycarbonateTubing: C-Flex; 30 cm (12 in.) length ID x OD: 9.7 x 12.7 mm (0.38 x 0.5 in.)Line 3End plug, polypropyleneTubing: C-Flex; 8 cm (3 in.) lengthID x OD: 6.35 x 10.92 mm (0.25 x 0.43 in.)3 portsSingle pack3 portsSingle packSingle pack—edge portsLine 1MPC insert, polycarbonateTubing: C-Flex; 8 cm (3 in.) lengthID x OD: 9.6 x 12.7 mm (0.378 x 0.50 in.)Line 2MPC insert, polycarbonateTubing: C-Flex; 8 cm (3 in.) lengthID x OD: 9.6 x 12.7 mm (0.378 x 0.50 in.)Line 3Injection portTubing: C-Flex; 8 cm (3 in.) lengthID x OD: 6.35 x 9.53 mm (0.25 x 0.375 in.)Note: Aegis5-14 film equivalents for this product areavailable as custom configurations.Line 1MPC insert, polycarbonateTubing: C-Flex; 46 cm (18 in.) lengthID x OD: 3.18 x 6.35 mm (0.125 x 0.25 in.)Line 2MPC body, polypropyleneTubing: C-Flex; 61 cm (24 in.) lengthID x OD: 9.53 x 15.875 mm (0.375 x 0.625 in.)Line 3Luer lock body connection, polypropyleneTubing: C-Flex; 61 cm (24 in.) lengthID x OD: 9.53 x 15.875 mm (0.375 x 0.625 in.)3 portsSingle pack—pillow design withpanel portsFind out more at /bpcFor Research Use or Further Manufacturing. Not for diagnostic use or direct administration into humans or animals.© 2021 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unlessotherwise specified. C-Flex and PharMed are trademarks of Saint-Gobain Performance Plastics. AdvantaFlex is a trademark of NewAge Industries, Inc. AseptiQuik is a trademark of Colder Products Company. Pall and Kleenpak are trademarks of Pall Corporation. ReadyMate is a trademark of Cytiva. SmartSite is a trademark of Becton, Dickinson and Company. Clave is a trademark of Victus Inc. Millipore is a trademark of Merck KGaA, Darmstadt, Germany and/or its affiliates. Meissner is a trademark of Meissner Filtration Products. Parker Bioscience is a trademark of Parker Hannifin Corp. Rubbermaid is a trademark of Rubbermaid Incorporated. Sartorius is a trademark of Sartorius AG. Specifications, terms, and pricing are subject toIndustry-standard Rubbermaid ™ totes with corresponding lids are available. They can be used to protect Labtainer BPCs up to 20 L in size during use, transport, and storage. Use standard 50 L drums for 50 L Labtainer BPCs.Tray with lidFlat-bottom, linear low-density polyethylene (LLDPE) drum with lid。
可朗妥安全数据表说明书
SECTION 1: Identification of the substance/mixture and of the company/undertaking1.1. Product Identifier Product name Canon Ink Tank CLI-581XL< C >Product Code(s)2049C1.2. Relevant identified uses of the substance or mixture and uses advised against UseInk for Ink Jet Printer1.3. Details of the supplier of the safety data sheet Supplier ImporterCanon Europa N.V.Bovenkerkerweg 59, 1185XB Amstelveen, The Netherlands +31 20 5458545, +31 20 5458222Manufacturer Canon Inc.30-2, Shimomaruko 3-Chome, Ohta-ku, Tokyo 146-8501, Japan 1.4. Emergency Telephone Number *1 Kontakt Giftlinien på tlf.nr.: 82 12 12 12 (åbent 24 timer i døgnet). Se punkt 4 om førstehjælp.*2 Only for the purpose of informing medical personnel in cases of acute intoxications.*3 Ask for Poison InformationSECTION 2: Hazards identification2.1. Classification of the substance or mixtureClassification according to Regulation (EC) No 1272/2008Not classified2.2. Label ElementsLabelling according to Regulation (EC) No 1272/2008112Safety Data SheetMalta 112Bulgaria Netherlands +31 (0)30-2748888 [*2]112Poland 112Version : 03Portugal +351 808 250 143CroatiaRomania +40 21 318 36 06+385 (0)1-23-48-342Slovakia +421 2 5477 4166Slovenia 112Cyprus Spain1121401Sweden 112 [*3]Issuing date : 19-Apr-2017United Kingdom 111 (UK only)Czech Republic Iceland 112+420 224919293Liechtenstein 145Norway+47 22 59 13 00Denmark Switzerland145+45 82 12 12 12 [*1]Estonia 16662SDS # : ICW 1784 R - 03 EU ENFinland +358 (0)9 471977France +33 (0)1 45 42 59 59Greece +30 210 7793777Austria Hungary +36 80 20 11 99+43 (0) 1 406 43 43Italy+39 (0)55 7947819Revision date : 31-Aug-2018Latvia+371 67042473Belgium Lithuania +370 687 53378+32 (0) 70 245 245LuxembourgHazard pictogramsNot requiredSignal wordNot requiredHazard statementsNot requiredPrecautionary statementsNot requiredOther InformationContains 1,2-benzisothiazol-3(2H)-one.May produce an allergic reaction.Contains less than 30% of components with unknown hazards to the aquatic environment.2.3. Other HazardsNoneSECTION 3: Composition/information on ingredients 3.2. MixturesChemical name CAS-No EC-No REACH registrationnumber Weight %Classification (Reg.1272/2008)Note toOtherHazardsGlycol CBI CBI CBI10 - 15NoneGlycerin56-81-5200-289-5None 5 - 10NoneUrea compound CBI CBI CBI 5 - 10Eye Irrit. 2 (H319)Substituted phthalocyanine salt CBI CBI CBI 1 - 5Eye Dam. 1 (H318)Aquatic Chronic 3 (H412) Water7732-18-5231-791-2None60 - 80NoneFull texts of Hazard statement(s) are listed in SECTION 16Note to Other Hazards : The following substance(s) is (are) marked with (1), (2) and/or (3)- (1) Substance for which EU Occupational Exposure Limit(s) is (are) established (See SECTION 8)- (2) PBT substance or vPvB substance under Regulation (EC) No 1907/2006- (3) Substance listed in Candidate List of SVHC for Authorisation under Regulation (EC) No 1907/2006In case a safety data sheet supplied under (EC) No 1907/2006 Article 31-3 is necessary, please contact us.SECTION 4: First aid measures4.1. Description of first aid measuresInhalation Move to fresh air. Get medical attention immediately if symptoms occur.Ingestion Rinse mouth. Drink 1 or 2 glasses of water. Get medical attention immediately if symptomsoccur.Skin Contact Wash off immediately with soap and plenty of water. Get medical attention immediately ifsymptoms occur.Eye Contact Flush with plenty of water. Get medical attention immediately if symptoms occur.4.2. Most important symptoms and effects, both acute and delayedInhalation None under normal use. Symptoms of overexposure are dizziness, headache, tiredness,nausea, unconsciousness, cessation of breathing.Ingestion None under normal use. Ingestion may cause gastrointestinal irritation, nausea, vomitingand diarrhea.Skin Contact None under normal use.Eye Contact None under normal use. May cause slight irritation.Chronic Effects None under normal use.4.3. Indication of any immediate medical attention and special treatment neededNoneSECTION 5: Firefighting measures5.1. Extinguishing mediaSuitable extinguishing mediaUse CO 2, water, dry chemical, or foam.Unsuitable extinguishing mediaNone5.2. Special hazards arising from the substance or mixtureSpecial HazardNoneHazardous combustion productsCarbon dioxide (CO 2), Carbon monoxide (CO)5.3. Advice for firefightersSpecial protective equipment for fire-fightersNoneSECTION 6: Accidental release measures6.1. Personal precautions, protective equipment and emergency proceduresAvoid contact with skin, eyes and clothing.6.2. Environmental PrecautionsKeep out of waterways.6.3. Methods and material for containment and cleaning upWipe up with adsorbent material (e.g. cloth, fleece).6.4. Reference to other sectionsNoneSECTION 7: Handling and storage7.1. Precautions for safe handlingAvoid contact with skin, eyes and clothing. Clean contaminated surface thoroughly. Use with adequate ventilation.7.2. Conditions for safe storage, including any incompatibilitiesKeep in a dry, cool and well-ventilated place. Keep out of the reach of children. Keep away from direct sunlight. Keep away from heat and sources of ignition.7.3. Specific end usesInk for Ink Jet Printer. Obtain special instructions before use.SECTION 8: Exposure controls/personal protection8.1. Control parameters Exposure LimitsChemical nameEU OEL Austria Belgium Bulgaria Cyprus Glycerin 56-81-5None None TWA: 10 mg/m 3None NoneChemical nameCzech Republic Denmark Finland France GermanyGlycerin 56-81-5TWA: 10 mg/m 3Ceiling: 15 mg/m 3NoneTWA: 20 mg/m 3TWA: 10 mg/m 3DFG TWA: 200 mg/m 3inhalable fraction Ceiling / Peak: 400mg/m 3 inhalablefraction Chemical nameGreece Hungary IrelandItaly NetherlandsGlycerin 56-81-5TWA: 10 mg/m 3None TWA: 10 mg/m 3 mist STEL: 30 mg/m 3 mistNone None Chemical namePoland PortugalRomania Slovakia SpainGlycerin 56-81-5TWA: 10 mg/m 3inhalable fractionTWA: 10 mg/m 3 mist NoneNone TWA: 10 mg/m 3 mistChemical nameSweden United Kingdom Norway Switzerland Turkey Glycerin 56-81-5NoneTWA: 10 mg/m 3 mistNoneTWA: 50 mg/m 3inhalable dust STEL: 100 mg/m 3inhalable dustNone8.2. Exposure controlsAppropriate engineering controlsNone under normal use conditions.Individual protection measures, such as personal protective equipmentEye/face ProtectionNot required under normal use.Skin ProtectionNot required under normal use.Respiratory ProtectionNot required under normal use.Thermal hazardsNot Applicable SECTION 9: Physical and chemical properties9.1. Information on basic physical and chemical properties AppearanceCyan ; Liquid OdorSlight odorOdor threshold No data available pH7 - 9Evaporation RateNo data availableNo data availableFlash Point (°C)> 93.0°C (Tag. Closed Cup.); estimated Melting/Freezing point (°C)No data available Boiling Point/Range (°C)Flammability (solid, gas)Not Applicable Flammability Limits in AirUpper Flammability Limit None; estimatedLower Flammability Limit None; estimatedVapor pressure No data availableVapor density No data availableRelative density 1.0 - 1.1Solubility(ies)Water; misciblePartition coefficient: n-octanol/water No data available Autoignition Temperature (°C)None; estimated Decomposition Temperature (°C)No data available Viscosity (mPa s) 1 - 5Explosive properties None; estimatedOxidizing properties None; estimated9.2. Other InformationNo data availableSECTION 10: Stability and reactivity 10.1. ReactivityNone10.2. Chemical stabilityStable10.3. Possibility of Hazardous ReactionsNone10.4. Conditions to AvoidNone10.5. Incompatible materialsAcids, Bases, Oxidizing agents, Reducing agents.10.6. Hazardous Decomposition ProductsCarbon dioxide (CO 2), Carbon monoxide (CO), and/or Ammonia.SECTION 11: Toxicological information 11.1. Information on toxicological effectsAcute toxicity No data availableSkin corrosion/irritation Non-irritant (Estimate) (OECD Guideline)Serious eye damage/eye irritation Minimal irritant (Estimate) (OECD Guideline) Sensitization Non-sensitizer (Estimate) (OECD Guideline)Germ cell mutagenicity Ames test: NegativeCarcinogenicity No data availableReproductive Toxicity No data available STOT - single exposure No data available STOT - repeated exposure No data available Aspiration hazard No data available Other InformationNo data availableSECTION 12: Ecological information12.1. Toxicity Ecotoxicity effects No data available12.2. Persistence and degradability No data available12.3. Bioaccumulative potential No data available 12.4. Mobility in soil No data available12.5. Results of PBT and vPvB assessmentThis preparation contains no substance considered to be persistent, bioaccumulating nor toxic (PBT).This preparation contains no substance considered to be very persistent nor very bioaccumulating (vPvB).12.6. Other adverse effects No data availableSECTION 13: Disposal considerations13.1. Waste treatment methodsDispose of in accordance with local regulations.SECTION 14: Transport information14.3. Transport Hazard Class 14.1. UN numberNone None 14.4. Packing Group None14.5. Environmental Hazards Not classified as environmentally hazardous under UN Model Regulations and marine pollutant under IMDG Code.14.2. UN Proper Shipping Name 14.6. Special Precautions for usersIATA: Not regulatedNoneSECTION 15: Regulatory information15.1. Safety, health and environmental regulations/legislation specific for the substance or mixture (EC) No 1907/2006 Authorisation Not regulated (EC) No 1907/2006 Restriction Not regulated (EC) No 1005/2009Not regulated (EC) No 850/2004Not regulated (EU) No 649/2012Not regulated Other InformationNone15.2. Chemical safety assessment NoneSECTION 16: Other informationFull text of H-Statements referred to under sections 2 and 3H318 - Causes serious eye damage H319 - Causes serious eye irritationH412 - Harmful to aquatic life with long lasting effectsKey literature references and sources for data- World Health Organization International Agency for Research on Cancer, IARC Monographs on the Evaluation on the Carcinogenic Risk of Chemicals to Humans- EU Regulation (EC) No 1907/2006, (EC) No 1272/2008, (EC) No 1005/2009, (EC) No 850/2004, (EU) No 649/2012Key or legend to abbreviations and acronyms used in the safety data sheet - PBT: Persistent, Bioaccumulative and Toxic - vPvB: very Persistent and very Bioaccumulative - SVHC: Substances of Very High Concern- EU OEL: Occupational exposure limits at Union level under Directive 2004/37/EC and (EU) 2017/2398, 98/24/EC, 91/322/EEC,2000/39/EC, 2006/15/EC, 2009/161/EU and (EU) 2017/164.- TWA: Time Weighted Average - STEL: Short Term Exposure Limit- GHS: Globally Harmonized System of Classification and Labelling of Chemicals - IARC: International Agency for Research on Cancer - IATA: International Air Transport Association - CBI: Confidential Business Information Issuing date :19-Apr-2017Revision date :31-Aug-2018Revision NoteSECTION 3 and 16 revisedThis product falls under (EC) No 1907/2006 Article 31-3.DisclaimerThe information provided on this SDS is correct to the best of our knowledge, information and belief at the date of its publication. The information given is designed only as a guide for safe handling, use, processing, storage,transportation, disposal and release and is not to be considered as a warranty or quality specification. The information relates only to the specific material designated and may not be valid for such material used in combination with any other material or in any process, unless specified in the text.14.7. Transport in bulk according to Annex II of MARPOL and the IBC CodeNot Applicable。
动物细胞组织细胞色素C释放凋亡检测试剂盒产品说明书(中
动物细胞/组织细胞色素C释放凋亡检测试剂盒产品说明书（中文版）主要用途动物细胞/组织细胞色素C释放凋亡检测试剂是一种旨在从动物细胞或活体组织中分离出线粒体和细胞浆组分，从而检测细胞色素C的转运，即由线粒体释放到细胞浆，来探测细胞凋亡的权威而经典的技术方法。
该技术经过精心研制、成功实验证明的。
适合于动物软组织（肝或脑组织）和硬组织（肌肉）以及培养细胞的线粒体和细胞浆组分的制备。
可以被用于后续蛋白质西方杂交等实验。
产品不含污染性蛋白水解酶和核酶，即到即用，性能稳定，分离到位，质量保证。
技术背景细胞色素C（CYTOCHROME C）在细胞凋亡中扮演着重要作用。
细胞色素C位于线粒体内外膜之间。
当细胞凋亡时，它从线粒体内释放到细胞浆里，引起一系列的信号通道的下游反应。
产品内容清理液（Reagent A）毫升裂解液（Reagent B）毫升净化液（Reagent C）毫升强化液（Reagent D）毫升保存液（Reagent E）毫升活性液（Reagent F）微升溶解液（Reagent G）毫升上样液（Reagent H）微升产品说明书1份保存方式保存净化液（Reagent C）和活性液（Reagent F）在-20℃冰箱里，避免反复冻融；其余的保存在4℃冰箱里；有效保证6月用户自备HANK平衡盐缓冲溶液（GMS12028）或PBS缓冲溶液（GMS12033）：用于清理细胞硬组织处理液（Reagent I）：用于促进硬组织表面溶解胰蛋白酶乙二胺四乙酸混合液（GMS12024）：用于细胞脱离完全细胞培养液（GMS12052）：用于细胞培养所需的培养基15毫升锥形离心管：用于样品操作的容器50毫升锥形离心管：用于样品操作的容器1.5毫升离心管：用于样品操作的容器4℃（微型）台式离心机：用于样品操作DOUNCE匀浆器：用于裂解组织细胞抗细胞色素C抗体：用于蛋白质西方杂交实验步骤一、动物软组织线粒体分离（组织匀浆法）实验开始前，将试剂盒里的活性液（Reagent F）冻融，然后移出xx微升活性液（Reagent F）和xx毫升净化液（Reagent C）到xx毫升的裂解液（Reagent B）里，混匀后，放进冰槽里，标记为裂解工作液。
荷尔登生物医学检测产品说明书
1mL
R
1mL
SST, R, GL
1mL
No capillary
1mL
collection
Order of Draw: 1. BLOOD CULTURES 2. LT BLUE 3. RED 4. SST 5. PST/LH GRN 6. LAV 7. GRAY
M2909 (1-19)
Microtainer Microtainer 1 mL
2 Microtainers Microtainer
2 mL FILL TO LINE 1 mL 1 mL Microtainer 1 mL 1 mL Microtainer
SST, R, GL
STAT to lab in 10 min
Also known as CMP SST, R, GL SST, R, GL
TOBRAMYCIN TOTAL PROTEIN TROPONIN TSH
TYPE AND CROSSMATCH
TYPE AND SCREEN URIC ACID
VANCOMYCIN VALPROIC ACID VITAMIN D
FEA
6LA LHC 6LIP
6LIVER 6LIPID LIA 6MG 6METX 6MONO PHNOC 6PFA 6PHOS 6PBNP 6PCAL 6KA 6PTIMEN PSAC 6PTT 6RETCT 6RENAL WHRIG 6SAL SYPHB TBSATA TT3C T4C TESTOC THEOC
CHEM8
QUICK CHEM 8 CBC/AUTO DIFF CKMB
COMP CREATININE CREATININE X-RAY EVALUATION D-DIMER DIGOXIN DILANTIN ELECTROLYTES FERRITIN FSH GLUCOSE
PLATE FORM
专利名称：PLATE FORM 发明人：KANEKO KOICHI,ABE KIYOTAKA,ICHINOSEKI
FUSAO 申请号：JP8710687 申请日：198704 10 公开号：JPS63255386A 公开日：19881021
摘要：PURPOSE:To permit installation of electrode plates in proximity to each other and to improve electrolytic efficiency by holding anode plates and cathode plates respectively by forms and arraying and disposing the anode plates and cathode plates integrally at every specified spacing. CONSTITUTION:A frame body 10 enclosing the side ends of the anode plates is formed of frame members 11, 12 and is provided with plural fixing parts 20. The fixing parts 20 are constituted of pawl-shaped projecting parts 21a, 21b and the anode plates 2 are inserted into the groove parts 22 thereof and are fixed by spring force. Spacings (about 1-2cm) where an electrolyte flows are formed between the members 11, 12 and the anode plate 2 side ends at this time. Short-circuit preventive parts 30 are projected to the upper part of the upper frames 11a, 12a and are hung from a cross bar. A pair of plate-shaped projecting pieces 41, 42 facing each other are formed on both side faces of the frame member 11. The side ends of the cathode plates 4 are grasped by these pieces 41, 42, by which the anode plates 2 and the cathode plates 4 are integrally arrayed and held at every prescribed spacing.
克洛克斯厨房洁净剂安全数据表说明书
_____________________________________________________________________________________________SAFETY DATA SHEETIssuing Date No data availableRevision Date 08-Sep-2020Revision Number 21. IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND OF THECOMPANY/UNDERTAKINGProduct identifier Product NameClorox® Toilet Bowl Cleaner Bleach - All Scents Other means of identification SynonymsNONEEPA Pesticide registration number 5813-89Recommended use of the chemical and restrictions on useRecommended UseToilet/Urinal Care Product - Non-aerosol Uses advised againstNo information available Details of the supplier of the safety data sheetSupplierThe Clorox Company Supplier Address1221 Broadway Oakland, CA 94612USATelephone1-510-271-7000Emergency telephone number Emergency Telephone NumberFor Medical Emergencies call: 1-800-446-1014. Transportation Emergencies, call Chemtrec: 1-800-424-93002. HAZARDS IDENTIFICATIONClassificationThis product is considered hazardous by the 2012 OSHA Hazard Communication Standard (29 CFR 1910.1200).Skin corrosion/irritation Category 2Serious eye damage/eye irritation Category 1GHS Label elements, including precautionary statementsEmergency OverviewSignal wordDangerHazard StatementsCauses serious eye damage Causes skin irritation.Precautionary Statements - PreventionWash face, hands and any exposed skin thoroughly after handlingWear protective gloves/protective clothing/eye protection/face protection Precautionary Statements - ResponseSpecific treatment (see supplemental first aid instructions on this label)EyesIF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing Immediately call a POISON CENTER or doctor/physician SkinIF ON SKIN: Wash with plenty of soap and water If skin irritation occurs: Get medical advice/attention Take off contaminated clothing and wash before reuse Precautionary Statements - Storage Not applicablePrecautionary Statements - Disposal Not applicableHazards not otherwise classified (HNOC)Not applicableUnknown Toxicity0.11 % of the mixture consists of ingredient(s) of unknown toxicity Other informationToxic to aquatic life with long lasting effects Very toxic to aquatic lifeInteractions with Other Chemicals No information available.Interactions with Other ChemicalsMay react with bleach-containing products or other household cleaners to produce hazardous gases.3. COMPOSITION/INFORMATION ON INGREDIENTSChemical Name CAS-No Weight-%Trade Secret Sodium hypochlorite 7681-52-91-5*Lauramine oxide 1643-20-50.1 - 1*Sodium hydroxide 1310-73-20.1 - 1*Myristamine oxide 3332-27-20.1 - 1**The exact percentage (concentration) of composition has been withheld as a trade secret4. FIRST AID MEASURESFirst aid measures General AdviceShow this safety data sheet to the doctor in attendance. Immediate medical attention is required. Do not get in eyes, on skin, or on clothing.Appearance Clear GreenPhysical state ViscousliquidOdor Multiple FragrancesEye contact If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes.Remove contact lenses, if present, after the first 5 minutes, then continue rinsing eye.Immediately call a POISON CENTER or doctor.Skin contact Wash with soap and water. Take off contaminated clothing and wash before reuse. Getmedical attention if symptoms occur.Inhalation Remove to fresh air. If symptoms persist, call a physician.Ingestion Drink 1 or 2 glasses of water. Do not induce vomiting without medical advice. Never giveanything by mouth to an unconscious person. Call a physician or poison control centerimmediately.Self-protection of the first aider Avoid contact with skin, eyes or clothing. Use personal protective equipment as required.Wear personal protective clothing (see section 8).Most important symptoms and effects, both acute and delayedBurning. Irritating.Most Important Symptoms andEffectsIndication of any immediate medical attention and special treatment neededNotes to Physician Treat symptomatically. Probable mucosal damage may contraindicate the use of gastriclavage.5. FIRE-FIGHTING MEASURESSuitable Extinguishing MediaUse extinguishing measures that are appropriate to local circumstances and the surrounding environmentUnsuitable extinguishing mediaCAUTION: Use of water spray when fighting fire may be inefficient.Specific hazards arising from the chemicalThe product causes irritation of eyes, skin and mucous membranes. Thermal decomposition can lead to release of irritating gases and vapors.Explosion DataSensitivity to Mechanical Impact None.Sensitivity to Static Discharge None.Protective equipment and precautions for firefightersAs in any fire, wear self-contained breathing apparatus pressure-demand, MSHA/NIOSH (approved or equivalent) and full protective gear.6. ACCIDENTAL RELEASE MEASURESPersonal precautions, protective equipment and emergency proceduresPersonal precautions Avoid contact with skin, eyes or clothing. Ensure adequate ventilation. Use personalprotective equipment as required. Wear self-contained breathing apparatus when enteringarea unless atmosphere is proved to be safe.Other Information Refer to protective measures listed in Sections 7 and 8.Environmental precautionsEnvironmental precautions See Section 12 for additional Ecological Information.Methods and material for containment and cleaning upMethods for containment Prevent further leakage or spillage if safe to do so.Methods for cleaning up Pick up and transfer to properly labeled containers.7. HANDLING AND STORAGEPrecautions for safe handlingHandling Handle in accordance with good industrial hygiene and safety practice. Avoid contact withskin, eyes or clothing. In case of insufficient ventilation, wear suitable respiratoryequipment. Use only with adequate ventilation and in closed systems. Do not eat, drink orsmoke when using this product. Take off contaminated clothing and wash before reuse. Conditions for safe storage, including any incompatibilitiesStorage Keep containers tightly closed in a dry, cool and well-ventilated place. Keep out of the reachof children.Incompatible products Toilet bowl cleaners, rust removers, acids, and ammonia-containing products.8. EXPOSURE CONTROLS/PERSONAL PROTECTIONControl parametersExposure Guidelines This product, as supplied, does not contain any hazardous materials with occupationalexposure limits established by the region specific regulatory bodiesChemical Name ACGIH TLV OSHA PEL NIOSH IDLHNone None None Sodium hypochlorite7681-52-9Lauramine oxideNone None None 1643-20-5Ceiling: 2 mg/m3TWA: 2 mg/m3IDLH: 10 mg/m3Ceiling: 2 mg/m3 Sodium hydroxide1310-73-2Myristamine oxideNone None None 3332-27-2Appropriate engineering controlsEngineering Measures ShowersEyewash stationsVentilation systemsIndividual protection measures, such as personal protective equipmentEye/face protection If splashes are likely to occur, wear safety glasses with side-shields.Skin and body protection Wear protective gloves and protective clothing. Long sleeved clothing.Respiratory protection If exposure limits are exceeded or irritation is experienced, NIOSH/MSHA approvedrespiratory protection should be worn. Positive-pressure supplied air respirators may berequired for high airborne contaminant concentrations. Respiratory protection must beprovided in accordance with current local regulations.Hygiene Measures Take off contaminated clothing and wash before reuse. Do not eat, drink or smoke whenusing this product. Contaminated work clothing should not be allowed out of the workplace.Wash thoroughly after handling.9. PHYSICAL AND CHEMICAL PROPERTIESInformation on basic physical and chemical propertiesPhysical state Viscous liquidAppearance Clear Green Odor Multiple Fragrances Color No information available Odor Threshold No information availableProperty Values Remarks MethodpH12.5 - 13.5None knownMelting / freezing point No data available None knownBoiling point / boiling range No data available None knownFlash Point Not flammable None knownEvaporation Rate No data available None knownFlammability (solid, gas)No data available None knownFlammability Limit in AirUpper flammability limit No data availableLower flammability limit No data availableVapor pressure No data available None knownVapor density No data available None knownSpecific Gravity~1.05None knownWater Solubility Soluble in water None knownSolubility in other solvents No data available None knownPartition coefficient: n-octanol/water No data available None knownAutoignition temperature No data available None knownDecomposition temperature No data available None knownKinematic viscosity No data available None knownDynamic viscosity~1000 cP None knownExplosive properties No data availableOxidizing properties No data availableOther InformationSoftening Point No data availableVOC Content (%)No data availableParticle Size No data availableParticle Size Distribution No data available10. STABILITY AND REACTIVITYReactivityNo data availableChemical stabilityStable under recommended storage conditions.Possibility of Hazardous ReactionsNone under normal processing.Conditions to avoidNone known based on information supplied.Incompatible materialsStrong oxidizing agents and Toilet bowl cleaners, rust removers, acids, and ammonia-containing products.Hazardous Decomposition ProductsNone known based on information supplied.11. TOXICOLOGICAL INFORMATIONInformation on likely routes of exposureProduct Information.Inhalation Inhaled corrosive substances can lead to a toxic edema of the lungs. Pulmonary edema canbe fatal. May cause irritation of respiratory tract.Eye contact Corrosive to the eyes and may cause severe damage including blindness. May causeirreversible damage to eyes.Skin contact Irritating to skin.Ingestion Ingestion may cause irritation to mucous membranes. Ingestion may cause gastrointestinalirritation, nausea, vomiting and diarrhea.Component InformationChemical Name LD50 Oral LD50 Dermal Inhalation LC50 Sodium hypochlorite8200 mg/kg (Rat)>10000 mg/kg (Rabbit)-7681-52-9---Lauramine oxide1643-20-5_1350 mg/kg (Rabbit)_Sodium hydroxide1310-73-2Information on toxicological effectsSymptoms May cause redness and tearing of the eyes. Erythema (skin redness). Burning. Coughingand/ or wheezing.Delayed and immediate effects as well as chronic effects from short and long-term exposureSensitization No information available.Mutagenic Effects No information available.Carcinogenicity The table below indicates whether each agency has listed any ingredient as a carcinogen.Component ACGIH IARC NTP OSHA-Group 3--Sodium hypochlorite7681-52-9 ( 1-5 )IARC (International Agency for Research on Cancer)Group 3 - Not Classifiable as to Carcinogenicity in HumansReproductive toxicity No information available.STOT - single exposure No information available.STOT - repeated exposure No information available.Chronic Toxicity Carcinogenic potential is unknown.Target Organ Effects Respiratory system. Eyes. Skin. Gastrointestinal tract (GI).Aspiration Hazard No information available.Numerical measures of toxicity Product InformationThe following values are calculated based on chapter 3.1 of the GHS documentNot applicable12. ECOLOGICAL INFORMATIONEcotoxicityVery toxic to aquatic life. Toxic to aquatic life with long lasting effects.Persistence and DegradabilityNo information available.BioaccumulationNo information availableOther adverse effectsNo information available.13. DISPOSAL CONSIDERATIONSWaste treatment methodsDisposal methods Dispose of in accordance with federal, state and local regulations.Contaminated Packaging Do not reuse empty containers. Dispose of in accordance with federal, state and localregulations.14. TRANSPORT INFORMATIONDOTDescription Not regulated per 49 CFR 171.4(c)(1)TDGDescription Not regulated per 49 CFR 171.4(c)(1)ICAO No information availableIATADescription Not restricted per IATA Special Provision A197IMDGDescription Not restricted per IMDG Code 2.10.2.7 Marine Pollutant exemption15. REGULATORY INFORMATIONInternational InventoriesTSCA All components are listed on the TSCA InventoryDSL All components are listed either on the DSL or NDSL.TSCA - United States Toxic Substances Control Act Section 8(b) InventoryDSL/NDSL - Canadian Domestic Substances List/Non-Domestic Substances ListUS Federal RegulationsSARA 313Section 313 of Title III of the Superfund Amendments and Reauthorization Act of 1986 (SARA). This product does not contain any chemicals which are subject to the reporting requirements of the Act and Title 40 of the Code of Federal Regulations, Part 372 SARA 311/312 Hazard CategoriesAcute Health Hazard YesChronic Health Hazard NoFire Hazard NoSudden release of pressure hazard NoReactive Hazard NoCWA (Clean Water Act)This product contains the following substances which are regulated pollutants pursuant to the Clean Water Act (40 CFR 122.21 and 40 CFR 122.42)Chemical Name CWA - ReportableQuantities CWA - Toxic PollutantsCWA - Priority PollutantsCWA - Hazardous SubstancesSodium hypochlorite7681-52-9100 lbXSodium hydroxide1310-73-21000 lbXCERCLAThis material, as supplied, contains one or more substances regulated as a hazardous substance under the Comprehensive Environmental Response Compensation and Liability Act (CERCLA) (40 CFR 302)Chemical Name Hazardous Substances RQsExtremely Hazardous Substances RQs RQSodium hypochlorite7681-52-9100 lb -RQ 100 lb final RQRQ 45.4 kg finalRQSodium hydroxide1310-73-21000 lb-RQ 1000 lb final RQRQ 454 kg finalRQUS State RegulationsCalifornia Proposition 65This product does not contain any Proposition 65 chemicals.U.S. State Right-to-Know RegulationsChemical Name New JerseyMassachusettsPennsylvaniaRhode IslandIllinoisSodium hypochlorite7681-52-9XXXXEPA StatementThis chemical is a pesticide product registered by the Environmental Protection Agency and is subject to certain labelingrequirements under federal pesticide law. These requirements differ from the classification criteria and hazard information required for safety data sheets, and for workplace labels of non-pesticide chemicals. Following is the hazard information as required on the pesticide label:EPA Pesticide labelDANGER: CORROSIVE. Causes irreversible eye damage. Causes skin irritation. Prolonged or frequently repeated skincontact may cause allergic reactions in some individuals. Do not get in eyes, on skin, or on clothing. For prolonged use, wear gloves. Wash thoroughly with soap and water after handling. Remove and wash contaminated clothing before reuse. Use only in well-ventilated areas.International RegulationsCanadaWHMIS Hazard Class Not determined16. OTHER INFORMATIONPrepared ByProduct Stewardship 23 British American tham, NY 121101-800-572-6501Revision Date 08-Sep-2020Revision NoteNo information availableDisclaimerThe information provided in this Safety Data Sheet is correct to the best of our knowledge, information and belief at NFPA Health Hazards 3Flammability 0Instability 0Physical andChemical Hazards -HMIS Health Hazards 3Flammability 0Physical Hazard 0Personal Protection Bthe date of its publication. The information given is designed only as a guidance for safe handling, use, processing, storage, transportation, disposal and release and is not to be considered a warranty or quality specification. The information relates only to the specific material designated and may not be valid for such material used in combination with any other materials or in any process, unless specified in the textEnd of Safety Data Sheet。
KODACHROME Film 处理方法手册说明书
3PROCESSING STEPSProcessing KODACHROME Film IntroductionThis section contains general information on films, chemicals, processing procedures, and process equipment used in Process K-14M. The methods and procedures described in this manual are presently recommended for processing KODACHROME Film. In some cases, even minor variations in these procedures and methods can cause significant degradation of film quality.Film StructureKODACHROME Films are reversal, subtractive color materials.When properly exposed and processed,they yield direct positive color images.The illustration on page3-4is a cross section(not to scale) of KODACHROME Film that illustrates changes to the film during the process sequence. The transparent support (film base) has an antihalation backing layer called rem-jet. The rem-jet minimizes reflections of exposing light off the inner surface of the support, once it has passed through the film layers. These reflections cause “halo” images and loss of apparent sharpness in the processed films. The rem-jet backing is removed during the processing cycle.The film base has a substratum (subbing layer) that provides adhesion of the light-sensitive emulsion layers to the film base. The subbing layer is followed by a red-sensitive emulsion,an interlayer,a green-sensitive emulsion, an interlayer,a yellow filter layer,a blue-sensitive emulsion, and finally, a protective gelatin overcoating. Although the red-sensitive layer is mainly sensitive to red light and the green-sensitive layer to green light, both of these emulsion layers are sensitive to blue light. The yellow filter layer absorbs the blue component of exposing light, preventing blue light exposure of the blue-green-sensitive and blue-red-sensitive emulsion layers.Film ExposureThe best photographic results are obtained when the film is exposed as recommended in the film instructions. The processing laboratory must then have a well-controlled process to provide the customer with the best possible slide or transparency.When the film is exposed, latent images are formed in each of the three emulsion layers. The blue-sensitive emulsion layer contains a record of the image created by the blue component of the exposing light; the green-sensitive layer contains the image formed by the green component; and finally, the red-sensitive layer contains the image formed by the red component of the exposing light. The records of the images are all formed simultaneously and are exactly superimposed.FilmsUse Process K-14M for the following 35 mm films:Processing StepsBacking Removal SolutionThe alkaline backing removal solution converts the rem-jet antihalation backing on the film base into a water-soluble form.This backing is removed in the backing removal wash. Backing Removal WashThis wash performs two functions:1.It removes the backing removal solution from the film.2.It completely removes the solubilized antihalationbacking from the base by a combination of wateraction and mechanical buffing.First Developer SolutionIn the first developer solution, the exposed silver halide grains (latent images) are reduced to metallic silver by the action of Phenidone* and hydroquinone developers:The resulting silver grains form three superimposed negative images of the original scene, one image in each of the red-, green-, and blue-sensitive emulsion layers. The remaining(unexposed and undeveloped)silver halide in the three emulsion layers constitutes the positive (reversal) images that are later converted to full-color images in the color-development phases of the process.First Developer WashThis wash stops the development and removes the first developer solution from the film.NameFilmCodeLetterCode KODACHROME 25 Film (Daylight)5073KM KODACHROME 64 Professional Film5033PKR KODACHROME 64 Film (Daylight)5032KR KODACHROME 200 Professional Film5002PKL KODACHROME 200 Film (Daylight)5001KL*Phenidone is a trademark of Ilford Limited.Ag+(ExposedSilverHalide)+Developer→Ag˚(NegativeSilverImages)+OxidizedDeveloper+X-(HalideIons)Red Reexposure Printing StepThe red reexposure printing step completely exposes all of the remaining silver halide in the red-sensitive (bottom)emulsion layer so that the silver halide develops completely in the cyan developer solution. At the same time, exposure of any remaining silver halide in the blue- and green-sensitive layers must be avoided to prevent unwanted cyan dye development in these layers. This selective exposure is obtained by printing through the base side of the film,using a properly selected red glass filter in the light beam. The green- and blue-sensitive emulsion layers have no intentional sensitivity to red light and should thereforeremain unaffected by the red-light exposure.However,some green-sensitive emulsion layers do have a slight, butsignificant, red sensitivity, and accurate control of the red printing intensity is necessary.Cyan Developer SolutionIn the cyan developer solution, a positive silver image is formed in the red-sensitive layer by the action of the color developing agent on the silver halide that was exposed during the red printing step.Simultaneously, the resulting oxidized color developercombines with the cyan coupler to form a positive cyan dye image. This image is deposited only in the red-sensitive emulsion layer.The simplified equations given above typify thedevelopment and coupling reactions that also take place in the yellow and magenta developer solutions. Actually, the reactions are more complex than indicated.If any red-sensitive halide is left undeveloped, unwanted dyes will be produced in the red-sensitive layer during later color development stages.Ag+X -(ExposedSilverHalide)+Color Developer →Ag˚(Positive Silver Images)+Oxidized Color Developer +X -(Halide Ions)Oxidized Color Developer+Coupler→Colored Dye ImageCyan Developer WashThis wash stops cyan development and removes the cyan developer solution from the film.Blue Reexposure Printing StepIn this printing step, all the remaining silver halide in the blue-sensitive top emulsion layer is exposed so that the silver halide develops completely in the yellow developer solution.At the same time,exposure of the remaining silver halide in the green-sensitive layer (which is also blue-sensitive)must be avoided to prevent unwanted yellow dye development in the green-sensitive layer.This selective exposure is obtained by printing through the emulsion surface of the film,using a properly selected blue glass filter in the light beam. The yellow filter layer between the blue- and green-sensitive layers limits passage of blue light from the emulsion side.However,the filter layer does not protect the green-sensitive layer from any stray blue printing light that may strike the base of the film.An optimum printing intensity for each printer should be established and then carefully controlled. Overprinting can result in unwanted exposure and subsequent yellow development of silver halide in the green-sensitive(magenta) layer. Underprinting leaves some of the silver halide in the yellow layer unexposed and subject to chemical exposure and development in the magenta developer.Either situation causes some degradation in quality.The selected levels of reexposure for both the red and blue printing steps are based on the results of actual photographic tests including each of the film types that are processed.These printer settings are computer controlled.For anything other than a lamp failure,call Kodak for service.Processing film with an inoperative printer produces unacceptable customer film.Yellow Developer SolutionIn the yellow developer solution, a positive silver image is formed in the blue-sensitive layer by the action of the color developing agent on the silver halide that was exposed during the blue printing operation. Simultaneously, a positive yellow dye image is formed by the reaction between the oxidized color developing agent and the yellow coupler. See the section,“Cyan Developer Solution”on page3-2for the generic equations.During the yellow development step, the blue-sensitive layer must be developed to completion while unwanted yellow development(fogging)of the green-sensitive layer is kept to a minimum. Any undeveloped silver halide in the blue-sensitive layer is developed in the magenta developer solution, causing magenta dye contamination in the yellow layer. Conversely, fogging of the green-sensitive layer during yellow development causes yellow dye contamination in the magenta layer and a significant reduction in the magenta dye yield. A normal ProcessK-14M yellow developer solution provides the required yellow and magenta separation.Normally, all of the exposed silver halide in the red-sensitive layer would be developed in either the first or the cyan developer solution.If any exposed silver halide in this layer remains undeveloped after the cyan developer solution, it is developed in the yellow developer solution,and results in yellow dye contamination in the cyan layer.Yellow Developer WashThis wash stops the yellow development and removes the yellow developer solution from the film.Magenta Developer SolutionAt this stage in the processing sequence, only the green-sensitive layer should contain any unexposed silver halide. Therefore,selective reexposure is unnecessary.The reversal agent in the magenta developer solution nucleates (chemically reexposes) all the remaining silver halide. During magenta development, a positive silver image is formed in the green-sensitive layer by the action of the color developing agent on the silver halide. Simultaneously, a positive magenta dye image is formed by the reaction of the oxidized color developing agent with the magenta coupler. See the section, “Cyan Developer Solution” on page 3-2. Magenta development is somewhat less critical than cyan and yellow development,because if the preceding steps were properly carried out, no silver halide should remain in the red- and blue-sensitive layers. Therefore, no unwanted magenta dye development should occur. However, if any silver halide is present in the red-or blue-sensitive layers,it is nucleated and developed in the magenta developer solution,producing magenta dye contamination of the cyan or yellow dye image.The silver halide in the green-sensitive layer is the most difficult to develop completely, and incomplete development results in an inadequate magenta dye image, especially in the maximum-density areas.Magenta Developer WashThis wash removes the magenta developer solution from the film.This is the most critical of all the wash steps because it is more difficult to remove the components of the magenta developer solution.ConditionerThe conditioner prepares the metallic silver developed in the first and color developers for oxidation to silver halide in the bleach step. An oxidized conditioner solution is ineffective and may cause silver to be retained in processed film. BleachThe bleach converts the metallic silver back to silver halide; the silver halide is later removed in the fixer.During bleaching, iron III is reduced to iron II. Iron II must be converted back to iron III by aeration so that satisfactory bleaching can continue. Aerate the bleach by bubbling air through it.Inadequate aeration, underreplenishment, low temperature, and over-dilution of the bleach by conditioner can cause silver retention, which causes all densities to increase.The silver may be removed by bleaching and fixing the film again, if necessary.FixerThe fixer converts all of the silver halide into soluble silver compounds. Most of the silver compounds are removed in the fixer and can be recovered. Underreplenishment,or fixer dilution,causes silver halide retention, increased blue density, or yellow D-min. The silver halide may be removed by bleaching and fixing the film again.Final WashThe final wash removes chemicals remaining in the film emulsion. Complete washing at this stage is important for image stability; any chemicals remaining in the film may deteriorate the image dyes.Final RinseThe final rinse contains a wetting agent to reduce water spotting and provide uniform drying.To help prevent water spots and streaks, replace the final rinse solution daily.Process SequenceP R O C E S S S E Q U E N C EW A S HF I XW A S H F I N A L R I N S ED R YR E D R E -E X P O S U R EW A S HS i l v e r H a l i d e i s R e m o v e dS i l v e r H a l i d e +F i xS o l u b l e S i l v e r C o m p l e xB L E AC HN E G A T I V E D E V E L O P E R E x p o s e d G r a i n s a r e D e v e l o p e d t o S i l v e r E x p o s e d S i l v e rH a l i d e D e v e l o p e r +S i l v e rS i l v e r i s C o n v e r t e d t o S i l v e r H a l i d eS i l v e r +B l e a c h i n g A g e n t +H a l i d eS i l v e r H a l i d eM A G E N T A D E V E L O P E RW A S H C O N D I T I O N E RB AC K I N G R E M O V A L P R E B A T H B A C K I N G R E M O V A L W A S H A n t i h a l a t i o n B a c k i n g i s R e m o v e d F o r m s M a g e n t aD y e i n M i d d l e L a y e r1. S i l v e r H a l i d e +R e v e r s a l A g e n t +D e v e l o p e rS i l v e r +O x i d i z e d D e v e l o p e r2. O x i d i z e d D e v e l o p e r +C o u p l e rM a g e n t a D y eY E L L O W D E V E L O P E RW A S HP r o c e s s K -14MA n t i h a l a t i o nB a c k i n g i s S o f t e n e dC A M E R A E X P O S U R EW A S HB L U E R E -E X P O S U R E B l u e L i g h tF o r m s L a t e n t I m a g e o n U n d e v e l o p e d S i l v e r H a l i d e i n T o p (B l u e -S e n s i t i v e )L a y e rB l a c kW h i t eL a t e n t I m a g e F o r m s o n E x p o s e d G r a i n s C Y A N D E V E L O P E R B l u e S e n s i t i v e Y e l l o w F i l t e r B l u e -G r e e n S e n s i t i v e B l u e -R e d S e n s i t i v eR A W S T O C KA C E T A T E S U P P O R TA n t i h a l a t i o nB a c k i n g F o r m sC y a nD y e i n B o t t o m L a y e r1. E x p o s e d S i l v e r H a l i d e +D e v e l o p e rS i l v e r +O x i d i z e d D e v e l o p e r2. O x i d i z e d D e v e l o p e r +C o u p l e rC y a nD y eK -14MR e d L i g h tF o r m s L a t e n t I m a g e o n U n d e v e l o p e d S i l v e r H a l i d e i n B o t t o m (R e d -S e n s i t i v e ) L a y e rF o r m s Y e l l o w D y e i n T o p L a y e r1. E x p o s e d S i l v e r H a l i d e +D e v e l o p e rS i l v e r +O x i d i z e d D e v e l o p e r2. O x i d i z e d D e v e l o p e r +C o u p l e rY e l l o w D y e。
卡迪克检测仪全能型
第 1 章 引言
感谢您选择了由 Polymer Technology Systems, Inc.（PTS）提供的 CardioChekTM P·A 检测仪。
CardioChekTM P·A 检测仪是一种便携式快速全血检测仪器。仪器由检测仪、MEMo 记忆芯片和检测条构成。 本仪器用于检测全血，供体外诊断之用。使用该仪器，医疗人员可快速测定样品中的各种血液成分。 CardioChekTM P·A 检测仪能够进行糖尿病和其它疾病状态及脂类筛选监测。
cardiochektm检测仪便携式全血检测仪器用户指南目录cardiochektmcardiochektm检测仪memo记忆芯片检测条电池安装语言设置时间设置声音设置日期设置单位设置打印机设置仪器检验15检查条质控执行检测17检测供应品检测
CardioChekTM P·A 检测仪 便携式全血检测仪器
显示屏（a） 显示屏显示检测结果、信息、时间、日期和保存的结果。
ENTER（输入）按钮 （b） 按此按钮开启检测仪或接受当前的菜单选择。
NEXT（下一个）按钮 （c） 按此按钮开启检测仪或继续下一菜单选项。 检测条插入口（d） 检测条插入口位于检测仪正面下方。检测条由此插入，凸面朝上。 MEMo 芯片端口（e） MEMo 芯片端口位于检测仪顶端。将 MEMo 芯片插入此端口，端口指状凹口（顶端）朝上。此端口还可用 于连接打印机。
仪器。
警告！安全弃置旧电池。
如何关掉检测仪： 因为检测仪的自动关机功能，电池使用期限延长。怠机 3 分钟后（未插入检测条），检测仪执行 10 秒倒计
时关机。如停止关机，按一个按钮（ 或 ）。在以下主菜单标题中的任意一个下：RUN TEST（执
行检测）、MEMORY（内存）、UTILITY（应用工具）和 USER SET（用户设置），同时按两个按钮（ 和
血细胞分析仪厂家库贝尔常用英语单词述语
real-time实时的multi-language多语种cross-contamination 交叉污染spare parts 备用件user interface 用户界面bio-medical field 生物医学领域reagent试剂self-lubricating 自润滑的lead rail 导轨recyclable可循环利用的multiple patents['pætnt]多项专利Chemiluminescence Immunoassay [,kem ɪ,l(j)u ːm ɪ'nes(ə)ns]CLIA化学发光免疫检测Radiology Immunoassay[re ɪd ɪ'ɒl əd ʒɪ]放射免疫检测cuvette[kju ː'vet]比色皿，透明小容器auto washing 自动清洗commitment承诺，保证intelligent test clew 智能测试提示detergent[d ɪ't ɝd ʒənt]清洁剂Touch screen触摸屏LCD touch screen液晶触摸屏LCD (liquid crystal display)液晶显示屏maintenance维修residual[r ɪ'z ɪdj ʊəl]残渣，残余volume体积accurate positioning精确定位applicable specimen['spes ɪm ɪn]适用的样本Blood serum['s ɪər əm]血浆，血清Blood plasma ['plæzm ə]血浆，血清whole blood全血cerebrospinal fluid脑脊髓液[,s ɛr əbro'spa ɪnl]dilute urine[d ɪ'lj ʊt]['ju ərin]稀释尿液Barcode scanner 条形码识别器，条形码扫描仪barcode['bɑrkod]条形码Microscope显微镜method-sample binomial 方法示例二项式 [ba ɪ'n əʊm ɪəl]univocal [,ju:ni'v əuk əl] 单义的，仅一种意思的，不含糊的reliability 可靠性stability 稳定性monitoring 监控evaluation评估internal database 内部数据库access进入retrieve[r ɪ'tri ːv]检索，恢复activator 催化剂，激活剂,活化剂priming起爆剂hydraulic system液压系统substrate['s ʌbstre ɪt]基质；酶作用物trigger扳机；[电子] 触发器；制滑机Vocabul2012-11-122012-11-13IVD(In Vitro Diagnostic)体外诊断Pump泵，抽水机diaphragm pump ['daiəfræm] 隔膜泵Optical sensor光学传感器temperature sensor 温度传感器magnetic sensor[mæg'netɪk][自]磁传感器sample plate/disk样品盘reagent plate/disk试剂盘reaction plate/disk反应盘incubator保温箱，培育箱，孵化盘detergent清洗液photodiode[,fəʊtəʊ'daɪəʊd]发光二极管spectrophotometer分光光度计[,spektrə(ʊ)fəʊ'tɒmɪtə]immunodiagnostic system免疫诊断系统analyte分析物，被分析物dilution稀释物acid liquid酸性液体alkali['ælkəlaɪ]碱liquid level detection液面检测collision protection防碰撞，碰撞防护low break down低故障refrigerated function制冷功能mechanical engineer机械工程师hardware engineer硬件工程师software engineer软件工程师monitor监视器driving problem驱动问题2012-11-14 macroscopical[mækrəu'skɔpikl]宏观的microcosmic/microscopic微观的reset instruction复位指令constraint force[kən'streint]约束力waste liquid level alarming废液液面报警器self-resetting function自动复位功能intelligent probe智能探针Optical Filter滤光片Mini Liter毫升colorimetric method比色（测定）法['kʌləri'metrik] colorimetric analysis比色分析colorimetric assay/determination比色测定increase reagent dose[dəʊs]增加试剂量EMI=electromagnetic interference电磁干扰 [i,lektrəumæɡ'netik] EMC=electromagnetic compatibility电磁兼容，电磁适应性Reading dial['daɪəl]读数盘chemical polishing化学抛光electrolytic polishing[机] 电解抛光 [ɪ,lektrəʊ'lɪtɪk] electropolishing 电解抛光[i'lektrəu'pɔliʃiŋ] electrobrightening电解抛光nitric acid[无化] 硝酸emit harmful gas散发出有害气体pernicious gas [pə'niʃəs]有害气体poisonous gas有毒气体distilled water[d ɪs't ɪld]蒸馏水validity check效果检测maximum test throughput最大测试量heat dissipation [disi'pei ʃən]散热cooling fan散热扇cholesterol[k ə'lest ər ɒl]胆固醇discrete分立式Optical cuvette 光学试管risk level 风险度Solid heating固体加热liquid level alarm function 液位报警功能reagent volume试剂量refrigerated reagent disk 冷藏试剂位sample position样本位electromagnetic valve 电磁阀switch on/off开/关机master switch/master switch 总开关Simulated assay模拟试验serial port/interface 串行端口，串口aspirate吸入barcode reading 条码阅读Polished Probe 抛光针Throughout生产量（测试量）cold treatment 冷疗法 bioelectrode 生物电极photodetector 光电检测管，光电探测器constant speed恒速Absorption range吸光度sample probe detection 样本针检测reaction volume 反应体积water consumption 耗水量endpoint method 终点法two-point method 两点法Fixed Time 固定时间法rate method速率法kinetics method [k ɪ'net ɪks; ka ɪ-] 动力学法colorimetric method['k ʌl əri'metrik]比色测定法，比色法non-linear curve[nɑn'l ɪn ɪɚ]非线性曲线calibration solution 标准液，定标液reagent consumption 试剂消耗量heat retaining panel 保温板insulation board保温板，绝缘板，隔热板drill a hole/ punch a hole 开孔，打孔catching cup抓杯Terminology & Abbreviation术语和缩写词（软件）ASTM Amercian Society for Testing and Material美国社会检测和材料CSF Cerebrospinal Fluid 脑脊液CSV Comma Separated ValuesCSV（逗号分隔值）文档EMC=electromagnetic compatibility 电磁适用性，兼容性EMI Electromagnetic Interference电磁干扰 [i,lektr əumæɡ'netik]2012-11-162012-11-152012-11-19GUI Graphical User Interface图形用户界面IVD(In Vitro Diagnostic)体外诊断LAN Local Area Network局域网LIS Location Information Server位置资MMI Man Machine Interface人机接口，人机界面MS Microsoft微软MTBF Mean Time Between Failure平均故障间隔时间OS Operative System操作系统RCM Risk Control Measures风险控制措施RFID Radio Frequency Identification无线电频率识别、无线射频识别RLU Relative Light Unit相对发光度单位/吸光值RH Relative Humidity相对适度SD Standard Deviation标准偏差TBC To be completed待完成的TBD To be defined待定义的UIRS User Interface requirements用户界面要求UPS Uninterruptible Power Supply不间断电源USB Universal Serial Bus通用串行接口/总线Instrument detection仪器检测Instrument testing仪器测试numerical reading读数supply voltage ['vəultidʒ]电源电压frequency/ rate频率power功率take out the cups取出杯子positive number正数minus/negative number负数molecule ['mɒlɪkjuːl][化学] 分子ion['aɪən]化学离子factor因子daily maintenance 日常维护alcohol content 酒精含量distortion失真saturation [sætʃə'reɪʃ(ə)n]饱和度fluctuations波动disposal处理，清理，安排reagent mixture试剂混合物on-going assay正在进行的试验univocally 意义明确地，单一地format格式，版本CSV file (commaseparated values file)CSV（逗号分隔值）文档LIS(location information server)位置资medicated plasters药用膏药photo'initiator光引发剂network node网络节点consistency一致性，相容性mismatching data不匹配的数据missing sample或缺的样本2012-11-20Other vocabverify the correctness of 验证…的正确性priority parameter 优先参数priority level优先等级decreasing order递减序列STAT（emergency)静；斯达(放射性强度单位)，紧急work list compilation工作表编辑work list priority scheduling工作表优先度排程reagent consumption estimation试剂消耗量评估intuitive presentation直观演示analytic system [ænə'lɪtɪk]分析系统systematic error系统误差，偏倚random error随机误差；偶然误差SD(standard deviation)标准偏差calibration curve validation校准曲线验证cartridge['kɑːtrɪdʒ]打印机的墨盒，笔芯，盒子clinical immunology [ɪmjʊ'nɒlədʒɪ]临床免疫学calibration curve recalculation校准曲线重新计算graph图表，曲线图result elaboration结果精华/详细阐述aging areas老化区defective goods/unaccepted product不合格品non-defective/qualified products合格品，良品overdue / out of date过期的expiration date [,ekspɪ'reɪʃ(ə)n]有效期clinical trials临床试验analytical methods分析方法background values本底值formaldehyde solution[fɔː'mældɪhaɪd]甲醛溶液optimize优化cabularyOptical diameter光学直径chemical reaction化学反应calibration校准，调试electrolyte Analyzer series['sɪəriːz]电解质分析仪系列[ɪ'lektrəlaɪt]applicable ions可适用离子deionized water [diː'aɪənaɪzd][化学] 去离子水instrument parameter仪器参数ambient temperature室温，环境温度Auto Chemistry Analyzer自动化学分析仪Auto Biochemistry Analyzer全自动生化分析仪hematology analyzer[,hemə'tɒlədʒɪ] 血液分析仪PM （Patient Monitor）监护仪Fetal Monitor ['fi:tl]胎儿监护仪Blood glucose meter['ɡlukos]血糖仪Hemoglobin Meter [,hiːməʊ'ɡləʊbɪn]血红蛋白检测仪，血红素检测仪Microplate Washer 洗板机Special Protein Analyzer['prəʊtiːn]特种蛋白分析仪Blood Gas Analyzer 血气分析仪coagulator[ko'ægjə,letɚ]凝血仪inner thermal printer内部热敏打印机probe探针human machine interaction人机交互Man machine interface人机界面Anti-collision stirrer防撞搅拌器waste liquid废液11-12 词汇diagnosis诊断Sample Rack样品架reagent bottle rack试剂瓶架workload工作量load new samples加载新样板unload卸载operator操作者，操作PCactuator执行机器，促动器，致动器actuator motor制动马达，驱动电动机assay[ə'seɪ; 'æseɪ]试验，分析，鉴定scheduled test预定的测试unfeasible不可实行的dispensing system 剂量器分配器reagent kit cartridge['kɑːtrɪdʒ]试剂盒depleted废弃的，耗尽的depletion 损耗，消耗，耗尽expiration[,ekspɪ'reɪʃ(ə)n]期满nearness接近，近似audible听得见的visible看得见的maximum the test throughput最大化测试吞吐量microcontroller[自] 微控制器system architecture definition phase系统架构定义阶段11-13 词汇subsystem 子系统；次要系统functionality功能，函数性concentration/density浓度user profile用户模版Washing station清洗工位Clinical diagnosis field临床诊断领域molecule ['mɒlɪkjuːl][化学] 分子；pneumatic[njuː'mætɪk]充气的，气胎calibrator[仪] 校准器；口径测量器,定标体FDA Food and Drug Administration （美国）食品及药物管理委员会Chemiluminescent Analyzer化学发光分析仪['kemi,lju:mi'nesənt]chemiluminescence化学发光，化学光independent Mixing Stirrer搅拌器，搅拌杆photometry[fəʊ'tɒmɪtrɪ]光度测定light source 光源reaction cuvette[kjuː'vet]反应试管，反应杯Graphical representation图解表示法Terminology and Abbreviation术语和缩写词Step motor driver步进电机驱动器stepping/stepper motor ['məutə]步进电机，步进马达brushless motor[电] 无刷电机；无刷马达dual-wavelength testing双波长测试parameter setting参数设置bubble气泡PCB =（Printed）circuit board（印刷）电路板absorbance unit吸光度单位resistance电阻11-14 词汇loading arm装载臂Assy ['æsi]组件Instruction inspection指令检验Synchronous belt ['sɪŋkrənəs]同步带synchronous pulley['pʊlɪ]同步带轮 ['siŋkrənəs]pipet[pɪ'pɛt]移液管,用移液管移Detector 检测器Halogen lamp ['hælədʒin] 卤素灯microliter微升colorimeter [,kʌlə'rɪmɪtə; ,kɒl-]色量计，色度计，色差仪centrifugal tube [sen'trifjuɡəl]离心管centrifugal [sen'trifjuɡəl]离心的；n. 离心机；转筒sealed cap密封盖specimen cup['spesɪmɪn] 标本杯suction tube吸管sample reagent probe样品试剂针Antibody抗体Hemocyte英['hiːməsaɪt]美['hɛməsaɪt]血细胞，血球Corrosive liquid [kə'rəusiv]腐蚀性液体calibration parameter调试参数calibration curve[自] 校准曲线，标准曲线raw data原始数据，原始资料system configuration系统配置configure all the parameters配置所有参数mechanical separation 机力分离，机械分离11-15 词汇syringe [sɪ'rɪn(d)ʒ; 'sɪ-]注射器，洗涤器syringe piston注射器活塞laser displacement sensor激光位移传感器UPS=uninterrupted power supply不间断电源Projector [prə'dʒektə]投影仪measuring cup量杯Thermo-controller温控器thermostat['θɜːməstæt]恒温器；自动调温器temperature control device温控装置constant恒定的resolution [rezə'luːʃ(ə)n]分辨率calibration method定标方法，校准法stirrer (rod)搅拌棒charging arm加液臂sample arm样本臂reagent arm试剂臂carry/transfer/transmitting arm传递臂noumenon['nuːmənɒn]本体，实体simultaneous testing items同时测试项目diluent['dɪljʊənt]稀释液magnetic bead磁珠tip head (sample taking tube)取样管,tip头cup rack杯架electrolytic solution 电解溶液[ɪ,lektrəʊ'lɪtɪk] wastewater treatment废水处理Maximum speed最大速度11-16 词汇TBA (total bile[baɪl] acid)总胆汁酸TP(total protein)总蛋白UA(urine acid)尿酸total bilirubin [,bɪlɪ'ruːbɪn]总胆红素Cr（creatinine [krɪ'ætɪniːn]）[生化] 肌酸酐，肌酐polymerase ['pɒlɪməreɪz; pə'lɪməreɪz] 聚合酶blood ammonia[ə'məʊnɪə]血氨urea nitrogen ['juəriə]['naitrədʒən] 尿素氮；脲氮urea nitrate 硝酸尿素Blood glucose ['ɡlu:kəus]血糖single/double reagent单/双试剂uninstall卸载软件，解除安装flux[flʌks]助焊剂plate washer water洗板水cap-decap device开盖合盖装置screenshot屏幕截图powerful machine[电] 强力电机low carry-over低携带污染prototype machine样机11-19 词汇composite control liquid复合控制液concentration / density 液体浓度performance testing性能测试Grating Photometry[fəʊ'tɒmɪtrɪ]光栅分光user-friendly noise reduction 用户友好的降噪Main board 主板transformer变压器Analog switch ['æn əl ɒɡ]模拟开关standby state备用状态，待命状态Quality control rule 质控规则Westgard multi-ruleWestgard多规则质控optical cuvette[kju ː'vet]光学试管，光度反应杯absorption cell 吸收池reset/restoration 复位Detection accuracy检测精确度three-dimensional Drive 3D转动，三维转动precise [pr ɪ'sa ɪs]精确的，精密的quality control chart 质控图graph[grɑːf; græf]图表；曲线图testing/inspection room 检测室guide rail 导轨，导杆signal信号induction/reaction principle 感应/反应原理susceptiveness [s ə'sept ɪvn ɪs]灵敏度 response ratemagnetic susceptibility 灵敏度，磁化率[s ə,sept ɪ'b ɪl ɪt ɪ]Ecuador ['ekw əd ɔ:]厄瓜多尔 [è guā duō ěr]Vietnam[,vjet'næm]越南Malaysia [m ə'lei ʒə]马来西亚Philippines ['filipi:nz] 菲律宾Brunei['bru:nai]文莱（东南亚苏丹国）Peru[p ə'r ʊ]秘鲁（拉丁美洲国家名）Columbia[k ə'l ʌmbi ə]哥伦比亚diaphragm ['da ɪəfræm] 隔膜；快门，光圈；隔板diaphragm pump隔膜泵ambient light['æmb ɪənt]背景光，环境光swab-off [sw ɒb]抽干amplifier放大器，扩音器accurate result精确的结果Grating Photometry[f əʊ't ɒm ɪtr ɪ]光栅分光user-friendly noise reduction 用户友好的降噪spaghetti[sp ə'get ɪ]意大利式细面条pharmaceutical[,fɑːm ə'su ːt ɪk(ə)l]药物，制药的pharmaceutical innovation 药物创新Progesterone Calset孕酮定标液progesterone [pr ə'd ʒest ər əʊn][生化] 黄体酮，[生化] 孕酮spectrophotometry[,spektr əuf əu't ɔmitri][分化][光] 分光光度法；[分化] 分光光度测定法reversed反转的，反向的parabola [p ə'ræb əl ə][数]抛物线polynomial多项式exponential [,eksp ə'nen ʃ(ə)l]指数的，指数calibration定标，测量口径solar powered mobile health-care unit太阳能移动医疗单位11-20 词汇vocabularyanalysis [ə'nælɪsɪs]分析；分解，验定analyze ['ænəlaiz] 对…进行分析，分解analytical [,ænə'litik,-kəl] 分析的；解析的；善于分析的suspend [sə'spend]延缓，推迟；使暂停；使悬浮discretionary QC酌情QC，自由决定的检测test tube试管test tube brush试管刷initialization初始化Composite calibration solution复合定标液Photometric anomaly alarm光度异常警报[ə'nɒm(ə)lɪ] Initial cup number起始杯号Blind value盲值Polyethylene foamed sheet 聚乙烯发泡片[,pɒlɪ'eθɪliːn] pearl cotton珍珠棉Chemical elements化学元素Periodic Table [化学]周期表potassium [pə'tæsɪəm][化学] 钾 (K)sodium ['səʊdɪəm][化学]钠（11号元素，符号Na）carbon [化学] 碳 <C>calcium['kælsɪəm][化学] 钙 <CA>lithium['lɪθɪəm] 锂（符号Li）silver银 （AG)oxygen氧 (O)nitrogen['naɪtrədʒ(ə)n][化学] 氮 （N)aluminum oxide ['ɔksaid]氧化铝=alumina[ə'luːmɪnə] calcium oxide['kælsɪəm][无化] 氧化钙，生石灰absolute ethyl alcohol['eθaɪl]无水乙醇、酒精（浓度大于99％(质量)的乙醇）fire extinguisher灭火器sanitation环境卫生，卫生设备。
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Analyze Phase - Continued
Propose adding stock to this surface
Analyze Phase - Continued
Root Cause Analysis: 1. Non-cleanup on the 1.01” flange surface after machining. a) Casting drawing does not provide adequate machine stock to ensure cleanup. b) Over arc & grind during riser removal.
DMAIC Problem Solving Report
Keokuk – Cameron Lower Plate 4” 600
Define Phase
Project Scope: Reduce defects after machining. Customer: Cameron Part Number: 1A-TZ03-506 Description: Lower Plate 4” 600 Class Problem Statement: Non-cleanup after machining. Problem Details: 1. Non-cleanup on the 1.01” flange surface after machining.
Defect Rate Charts:
YTD Shipped vs Rejected
180 160 140 120 100 80 YTD Shipped YTDYTD Rejected
Analyze Phase
Charts/Diagrams (Pareto, Scatter Diagram, Ishikawa Diagram, Current Equipment, Etc.):
Example Photos:
Measure Phase
Current Defect Rates: 1. Non-cleanup on the O.D. of the flange. a) 26 out of 168 castings have had non-cleanup on the 1.01” surface of the flange. b) 15.5% of castings have had non-cleanup on the 1.01” surface of the flange.
Heat code after corrective action to track for validation: To be determined
Control Phase
Update Process Documentation: 1. Non-cleanup on the 1.01” flange surface after machining. a) Update drawing and pattern records to reflect added stock. b) Update control plan, work instructions and train employees on use of template.
Improve Phase
Corrective Action Plan: 1. Non-cleanup on the 1.01” flange surface after machining. a) Propose adding 0.170” stock to the 1.01” flange surface to customer. b) Provide profile template for arc and grind operation to prevent removing too much material during riser removal.