DS-413-A Determination of pH in an aqueous extract
Toilet Duck Mr Muscle 反渗透垫浴缸清洁剂 EU版2.0 安全数据表说明书
Toilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.0011. IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND OF THE COMPANY/UNDERTAKING1.1 Product identifier : Toilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EU1.2 Relevant identified uses of the substance or mixture and uses advised againstUse of the Substance/Mixture : Washing and cleaning products (including solvent based products)Uses advised against : None identified1.3 Details of the supplier of the safety data sheet : SC Johnson Ltd.Frimley GreenCamberleyGU16 7AJTelephone : +441276852000 E-mail address : **************1.4 Emergency telephone number : Consumer Care Center: UK - 0800 353 353Ireland - 1800 409 1762. HAZARDS IDENTIFICATION2.1Classification of the substance or mixtureClassification according to Regulation (EU) 1272/2008 with the correlation table 67/548/EEC or 1999/45/EC (Annex VII of CLP)2.2 Label elementsLabelling according to Regulation (EC) No. 1272/2008 (CLP)Hazard symbolsToilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001Signal wordDangerHazard statements(H314) Causes severe skin burns and eye damage.(H410) Very toxic to aquatic life with long lasting effects.(H290) May be corrosive to metals.Precautionary statements(P101) If medical advice is needed, have product container or label at hand.(P102) Keep out of reach of children.(P260) Do not breathe fume.(P310) Immediately call a POISON CENTER or doctor/ physician.(P305 + P351 + P338) IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.(P301 + P330 + P331) IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.(P304 + P340) IF INHALED: Remove person to fresh air and keep comfortable for breathing.(P303 + P361 + P353) IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower.(P405) Store locked up.(P280) Wear protective gloves / eye protection.(P264) Wash hands thoroughly after handling.Additional LabellingFor use only in toilet bowls.As with any household product avoid prolonged skin contact with this productDo not mix with bleach or any other household cleaners.Detergents regulations : Contains< 5%non-ionic surfactants, perfume2.3 Other hazards: None identified3. COMPOSITION/INFORMATION ON INGREDIENTS3.2 MixturesHazardous componentsToilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001Additional InformationFor the full text of the H-Statements mentioned in this Section, see Section 16.4. FIRST AID MEASURES4.1 Description of first aid measuresInhalation : Move to fresh air.Get medical attention immediately.Skin contact : Take off all contaminated clothing immediately.Immediately flush skin with large amounts of water.Get medical attention if irritation develops and persists.Wash contaminated clothing before re-use.Toilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001 Eye contact : Remove contact lenses.Protect unharmed eye.Keep eye wide open while rinsing.Flush immediately with plenty of water for at least 15 to 20 minutes.Ingestion : Do NOT induce vomiting.Rinse mouth with water.Get medical attention immediately.Never give anything by mouth to an unconscious person.4.2 Most important symptoms and effects, both acute and delayedEyes : Causes serious eye damage.No adverse effects expected when used as directed.Skin effect : Causes severe skin burns.No adverse effects expected when used as directed.Inhalation : Do not mix with bleach or any other household cleaners.May cause respiratory tract irritation.No adverse effects expected when used as directed.Ingestion : Causes digestive tract burns.No adverse effects expected when used as directed.4.3 Indication of any immediate medical attention and special treatment neededSee Description of first aid measures unless otherwise stated.5. FIREFIGHTING MEASURES5.1 Extinguishing mediaSuitable : Use extinguishing measures that are appropriate to local circumstancesand the surrounding environment.Unsuitable : None identified5.2 Special hazards arising from the substance or mixture : In case of fire and/or explosion do not breathe fumes.Exposure to decomposition products may be a hazard to health.5.3 Advice for firefighters: In the event of fire, wear self-contained breathing apparatus.Wear suitable protective clothing and gloves.Refer to current EN or National standard as appropriate.Toilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EU Version 2.0Print Date 26.04.2017Revision Date 09.03.2015Specification Number : 350000025059SITE FORM Number :30000000000000017761.0016. ACCIDENTAL RELEASE MEASURES6.1 Personal precautions, protective equipment and emergency procedures :Use personal protective equipment.6.2 Environmental precautions:Prevent product from entering drains.Do not flush into surface water or sanitary sewer system. Prevent further leakage or spillage if safe to do so.If the product contaminates rivers and lakes or drains inform respective authorities.Use appropriate containment to avoid environmental contamination.6.3 Methods and materials for containment and cleaning up:Soak up with inert absorbent material (e.g. sand, silica gel, acid binder, universal binder, sawdust). Clean residue from spill site.Keep in suitable, closed containers for disposal.6.4 Reference to other sections:For personal protection see section 8. For disposal considerations see section 13.7. HANDLING AND STORAGE7.1 Precautions for safe handling: For personal protection see section 8. Avoid contact with skin and eyes.Smoking, eating and drinking should be prohibited in the application area. Wear personal protective equipment.Normal measures for preventive fire protection.7.2 Conditions for safe storage, including any incompatibilities: Do not freeze.Keep out of the reach of children.Store away from food, beverages and pet food. No decomposition if stored and applied as directed.7.3 Specific end use(s): Consumer uses: Private households (= general public = consumers)Washing and cleaning products (including solvent based products)8. EXPOSURE CONTROLS/PERSONAL PROTECTION8.1 Control parametersToilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001Refer to current EN or National standard as appropriate.8.2 Exposure controlsRespiratory protection : In the case of vapour formation use a respirator with an approved filter.Hand protection : Wear suitable gloves.The selected protective gloves have to satisfy the specifications of EUDirective 89/686/EEC and the standard EN 374 derived from it.Before removing gloves clean them with soap and water.Eye/face protection : Safety glassesSkin and body protection : Wash contaminated clothing before re-use.Other information : Wash hands before breaks and at the end of workday.Environmental Exposure Controls : Refer to section 6.9. PHYSICAL AND CHEMICAL PROPERTIES9.1 Information on basic physical and chemical propertiesAppearance : liquidColour : greenOdour : greenOdour Threshold : No data availablepH : < 1Melting point/freezing point : No data availableInitial boiling point and boiling range : 100 °CToilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001Flash point : > 100 °CEvaporation rate : No data availableFlammability (solid, gas) : Does not sustain combustion.Upper/lower flammability or: No data availableexplosive limitsVapour pressure : No data availableVapour density : No data availableRelative density : 1.03 - 1.05 g/cm3Solubility(ies) : soluble: No data availablePartition coefficient: n-octanol/waterAuto-ignition temperature : Test not applicable for this product typeDecomposition temperature : No data availableViscosity, dynamic: 500 - 800 mPa.sat 25 °CViscosity, kinematic: No data availableExplosive properties : No data availableOxidizing properties : No data availableOther information : None identified : 10. STABILITY AND REACTIVITY10.1 Reactivity: Do not mix with bleach or any other household cleaners.10.2 Chemical stability : Stable under recommended storage conditions.: Do not mix with bleach or any other household cleaners.10.3 Possibility of hazardousreactions10.4 Conditions to avoid: Extremes of temperature and direct sunlight.10.5 Incompatible materials: Do not mix with bleach or any other household cleaners.Toilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001: No decomposition if stored and applied as directed.10.6 Hazardous decompositionproducts11. TOXICOLOGICAL INFORMATIONInformation on toxicological effectsAcute inhalation toxicityNo data availableSkin corrosion/irritation : Causes severe skin burns.: Causes serious eye damage.Serious eye damage/eyeirritationSkin sensitisation : Based on available data, the classification criteria are not met.Germ cell mutagenicity : Based on available data, the classification criteria are not met.Carcinogenicity : Based on available data, the classification criteria are not met.Toxicity for reproduction : Based on available data, the classification criteria are not met.STOT - single exposure : Based on available data, the classification criteria are not met.STOT - repeated exposure : Based on available data, the classification criteria are not met.Toilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001Aspiration hazard : Based on available data, the classification criteria are not met.12. ECOLOGICAL INFORMATIONProduct : The product itself has not been tested.12.1ToxicityToxicity to fishToxicity to aquatic invertebratesToilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.00112.2Persistence and degradability12.3Bioaccumulative potential12.4Mobility12.5PBT and vPvB assessment12.6Other adverse effects : None known.13. DISPOSAL CONSIDERATIONS13.1 Waste treatment methodsProduct : Do not dispose of waste into sewer.Do not contaminate ponds, waterways or ditches withchemical or used container.Disposal should be in accordance with local, state ornational legislation.Please recycle empty packaging.Toilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EU Version 2.0Print Date 26.04.2017Revision Date 09.03.2015Specification Number : 350000025059SITE FORM Number :30000000000000017761.001Packaging:Do not re-use empty containers.14. TRANSPORT INFORMATION15. REGULATORY INFORMATION15.1 Safety, health and environmentalregulations/legislation specific for the substance or mixture :This safety datasheet complies with the requirements of Regulation (EC) No. 1907/2006.16. OTHER INFORMATIONIf applicable, revision(s) are noted by the bold bars || in left-hand margin. Further informationToilet Duck / Mr Muscle Anti-Limescale Manual Toilet Bowl Cleaner EUVersion 2.0 Print Date 26.04.2017 Revision Date 09.03.2015 Specification Number: 350000025059SITE FORM Number:30000000000000017761.001The information provided in this Safety Data Sheet 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 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 text.。
ISORUST AM-DS 413 MSDS
1.化学产品和公司标识化学品中文名称:防锈油化学品英文名称:Water Displacement Antirust Oil企业名称:优力萌应用材料(上海)有限公司地址:上海市普陀区古浪路1570弄3号一楼传真号码:(国家或地区代码)(区号)021(电话号码)51697899-866 企业应急电话:(国家或地区代码)(区号)021(电话号码)51697899 技术说明书编码:413生效日期:2013年1 月1日2.组成/成份资料3.危害标识健康危害性对身体有害:吞入后会造成肺部损伤。
经常不断接触下会对皮肤造成乾疙及分裂。
物理和化学危害性/火灾和爆炸的危险轻度危险:该物质只有在加热至其闪点或高于其闪点温度时会形成可燃性混合物或燃烧。
静电放电:产品会积累静电,发生闪火的电火花。
4.急救措施吸入:使用合适的呼吸防护装置,立即将有关患者转移。
若患者呼吸停止,须进行人工呼吸。
保持休息状态,及时进行医护。
皮肤接触:用大量清水冲洗,如有可能请使用香皂。
除去大部分被污染的衣物,包括鞋子等。
再次穿着前须洗净。
眼睛接触:用大量清水冲洗眼睛直至刺激感消退。
如果刺激感仍然持续,需进行医疗处理。
误食:若发生吞服,勿催吐。
保持休息状态,及时进行医护。
5.灭火措施灭火步骤:用水喷洒冷却火焰触及的表面,并保护人员安全。
切断“燃料”源。
用泡沫、干粉化合物或水喷洒灭火。
特殊防火警告不要将水直接喷洒进贮存容器中,这样做会造成暴沸的危险。
有害燃烧物烟、雾、氮氧气体、碳氧化物。
防护装备:消防人员穿戴防护服,护目镜及呼吸保护装置。
6.意外溢漏处理措施地面溢漏:隔离人群。
无危险的情况下,尽可能切断危害源。
若物质进入水网或下水道,或污染了土地或作物,必须通知有关单位。
采取措施将其对下水的影响控制在最小限度。
用黄砂和泥土吸附溢漏液体。
用泵(使用防爆型或手动泵)或适当的吸收材料回收。
若液体太粘而不能泵送,则用铲和小桶铲起并置于适当的容器中回收或废弃。
Crafter’s Choice白砂土说明书
Safety Data Sheet Crafter’s Choice™ White Kaolin ClaySection 1: Identification of the Substance/Preparation and the Company Product Name : Crafter’s Choice™ White Kaolin Clay CAS Number: 1332-58-7 EC Number: 310-194-1 Applications Identified uses: Functional additive Details of the supplier of the safety data sheet: Crafter’s Choice Brands, LLC 7820 E. Pleasant Valley Road Independence, OH 44131 (800) 908-7028 Emergency telephone number: ChemTel (MIS3548100) (800) 255-3924 Domestic USA, Canada, Puerto Rico, USVI + (813) 248-0585 International Section 2: Hazards Identification Classification of the substance or mixture Classification according to Regulation (EC) 1272/2008 (EU 'CLP' regulation) Not classified as hazardous Classification according to Regulation (EC) No. 1272/2008[CLP] Not classified as hazardous. Classification according to Directive 67/5481EEC or 19991451EC Not classified as hazardous. Adverse physiochemical, human health and environmental effects Depending on the type of handling and use (e.g. grinding, drying), airborne respirable crystalline silica may be generated. Prolonged and/or massive Inhalation of respirable crystalline silica dust may cause lung fibrosis, commonly referred to as silicosis.Principal symptoms of silicosis are cough and breathlessness. Occupational exposure to respirable crystalline silica dust should be monitored and controlled. The product is not expected to be hazardous to the environment.Label elements Labelling according to Regulation (EC) 1272/2008 (EU 'CLP' regulation) Risk Phrases NC Not Classified Safety Phrases NC Not ClassifiedRevision Date: 09/25/2015Section 3: Composition and Information on IngredientsSubstancesSection 4: First-aid MeasuresDescription of first aid measuresGeneral advice No acute and delayed symptoms and effects are observed.Inhalation Move-into fresh air and keep at rest. Get medical attention if any discomfort continues.If swallowed Rinse mouth thoroughly. Get medical attention if any discomfort continues.Skin contact Wash skin with soap and water. Use suitable lotion to moisturize skin.Eye contact Do not rub eye. Rinse with large quantities of water. Get medical attention if irritation persists.Most important symptoms and effects, both acute and delayedGeneral informationIf adverse symptoms develop as described, transfer the casualty to a hospital as soon as possible.Indication of any immediate medical attention and special treatment neededNo specific first aid measures noted.Section 5: Fire-fighting MeasuresExtinguishing mediaThis product is non-combustible. No specific extinguishing media is needed.Special hazards arising from the substances or mixtureNon-combustible. No hazardous thermal decomposition.Advice for fire-fightersNo specific fire-fighting protection is required. Use an extinguishing agent suitable for the surrounding fire. Section 6: Accidental Release MeasuresPersonal precautions, protective equipment and emergency proceduresGeneral measuresAvoid airborne dust generation. Wear personal protective equipment incompliance with national legislation.Avoid dry sweeping and use water spraying or vacuum cleaning systems to prevent airborne dust generation. Wear personal protective equipment in compliance with national legislation.Reference to any other sectionsFor personal protection, see section 8. For waste disposal, see section 13.Section 7: Handling and StoragePrecautions for safe handlingAvoid airborne dust generation. Provide appropriate exhaust ventilation at places where airborne dust is generated. In case of insufficient ventilation, wear suitable respiratory protective equipment. Handle packaged products carefully to prevent accidental bursting. If you require advice on safe handling techniques, please contact your supplier or check the Good Practice Guide referred to in section 16. Do not to eat, drink and smoke in work areas; wash hands after use; remove contaminated clothing and protective equipment before entering eating areas.Conditions for safe storage, including any incompatibilitiesStore in a dry covered area. Minimize airborne dust generation and prevent wind dispersal during loading and unloading. Keep containers closed and store packaged products so as to prevent accidental bursting.Specific end use(s)Usage DescriptionIf you require advice on specific uses, please contact your supplier or check the Good Practice Guide referred to in section 16.Section 8: Exposure Controls/Personal ProtectionControl parametersExposure controlsEngineering measuresMinimize airborne dust generation. Use process enclosures, local exhaust ventilation or other engineering controls lo keep airborne levels below specified exposure limits. If user operations generate dust, fumes or mist, use ventilation to keep exposure lo airborne particles below the exposure limit. Apply organizational measures, e.g. by isolating personnel from dusty areas. Remove end wash soiled clothing.Respiratory equipmentIn case of prolonged exposure to airborne dust concentrations, wear a respiratory protective equipment that complies with the requirements of European or national legislation.Use eye protection. Goggles/face shield are recommended. Contact lenses should not be worn when working with this product.Hygiene measuresWhen using, do not eat, drink or smoke. Wash hands at the end of each work shift and before eating, smoking and using the toilet.Use appropriate skin cream to prevent drying of skin.Skin protectionNo specific requirement. Appropriate protection (e.g. protective clothing, barrier cream) is recommended for workers who suffer from dermatitis or sensitive skin.Section 9: Physical and Chemical PropertiesInformation on basic physical and chemical propertiesAppearance LumpColor White / Off-whiteOdor Almost odorlessSolubility Insoluble in waterRelative density 2.6 – 2.7Other InformationNo information requiredSection 10: Stability and ReactivityReactivityNo specific reactivity hazards associated with this product.Chemical stabilityStable under normal temperature conditions and recommended use.Possibility of hazardous reactionsNot applicable.Conditions to avoidNo particular incompatibilityIncompatible materialsNo specific, or groups of materials are likely to react to produce a hazardous situation.Hazardous decomposition productsNone under normal conditions.Section 11: Toxicological InformationInformation on toxicological effectsAcute toxicity This product has low toxicity. Only large volumes may haveadverse impact on human health.Skin corrosion / irritation Prolonged contact may cause dryness of skinSerious eye damage / eye irritation Particles in the eyes may cause inflammation and smarting Respiratory or skin sensitization Dust in high concentrations may irritate the respiratory system Germ cell mutagenicity Not classifiedCarcinogenicity Not classifiedReproductive toxicity Not classifiedSpecific target organ toxicity – single exposure Not classifiedSpecific target organ toxicity – repeated exposure Not classifiedAspiration hazard Not classifiedSection 12: Ecological InformationToxicityLC 50, 96 Hrs. Fish mg/l >1000EC 50, 48 Hrs. Daphnia, mg/l >1000IC 50, 72 Hrs. Algae, mg/l >1000Persistence and biodegradabilityThe product is not biodegradable.Bio-accumulative potentialThe product does not contain any substances expected to be bio-accumulating.Mobility in soilThe product is insoluble in water.Results of PBT and vPvB assessmentNot Classified as PBT/vPvB by current EU criteriaOther adverse effectsEcotoxicityThe product components are not classified as environmentally hazardous. However, this does not exclude the possibility that large or frequent spills can have a harmful or damaging effect on the environment.Section 13: Waste Disposal InformationGeneral InformationThis mineral can be disposed of as a nontoxic/inactive material in approved landfill sites in accordance with local regulations. Dust formation from residues in packaging should be avoided and suitable worker protection assured. Store used packaging in enclosed receptacles. Recycling and disposal of packaging should be carried out in compliance with local regulations. The re-use of packaging is not recommended. Recycling and disposal of packaging should be carried out by an authorized waste management company.Waste treatment methodsWhere possible, recycling is preferable to disposal. Can be disposed of in compliance with local regulations.Section 14: Transport InformationUN NumberNo information requiredTransport hazard class(es)No information required.Packaging groupNo information required.Environmental hazardsEnvironmentally Hazardous Substance / Marine Pollutant - No.Special precautions for userNot applicableTransport In bulk according to Annex U of MARPOL 73178 and IBC CodeNo Information required.Section 15: Regulatory InformationSafety, health and environmental regulations/legislation specific for the substance or mixtureUK Regulatory ReferencesHealth and Safety at Work Act 1974. The Control of Substances Hazardous to Health Regulations 2002 (S.I 2002 No. 2677) with amendments.Statutory InstrumentsThe Chemicals (Hazard Information and Packaging for Supply) Regulations 2009 (S.I 2009 No. 716).Approved Code of PracticeSafety Data Sheets for Substances and Preparations. Classification and Labelling of Substances and Preparations Dangerous for Supply.EU-RegulationsExempted in accordance with Annex V.7National regulationsWorkplace exposure Limits 2005 (EH40)Water hazard classificationNWGChemical safety assessmentNo chemical safety assessment has been carried out.Section 16: Additional InformationGeneral informationWorkers must be informed of the presence of crystalline silica and trained in the proper use and handling of this product as required under applicable regulations.A multi-sectoral social dialogue agreement on Workers Health Protection through the Good Handling and Use of Crystalline Silica and Products Containing It was signed on 25 April 2006. This autonomous agreement, which receives the European Commission’s financial support, is based on a Good Practices Guide. The requirements of the Agreement camehttp://www.nepsi.eu and provide useful Information and guidance for the handling of products containing respirable crystalline silica. Literature references are available on request from EUROSIL, the European Association of Industrial Silica Producers.Prolonged and/or massive exposure to respirable crystalline silica-containing dust may cause silicosis, a nodular pulmonary fibrosis caused by deposition in the lungs of fine respirable particles of crystalline silica.In 1997, IARC (the International Agency for Research on Cancer) concluded that crystalline silica inhaled from occupational sources can cause lung cancer in humans. However it pointed out that not all industrial circumstances, nor all crystalline silica types were to be incriminated. (IARC Monographs on the evaluation of the carcinogenic risks of chemicals to humans, Silica, silicates dust and organic fibers, 1997, Vol. 68, IARC, Lyon, France.)In June 2003, SCOEL (the EU Scientific Committee on Occupational Exposure Limits) concluded that the main effect in humans of the inhalation of respirable crystalline silica dust is silicosis. "There is sufficient information to conclude that the relative risk of lung cancer is increased in persons with silicosis (and, apparently, not in employees without silicosis exposed to silica dust in quarries and in the ceramic industry. Therefore preventing the onset of silicosis will also reduce the cancer risk…” (SCOEL SUM Doc 94 - final, June 2003).So there is a body of evidence supporting the fact that increased cancer risk would be limited to people already suffering from silicosis. Worker protection against silicosis should be assured by respecting the existing regulatory occupational exposure limits and Implementing additional risk management measures where required.Health & Safety Executive: Detailed reviews of the scientific evidence on the health effects or crystalline silica have been published by HSE (Health and Safety Executive, UK) in the Hazard Assessment Documents EH75/4 (2002) and EH75/5 (2003). The HSE points out on its website that Workers exposed to fine dust containing quartz are at risk of developing a chronic and possibly severely disabling lung disease known as "silicosis”. In addition to silicosis, there is now evidence that heavy and prolonged workplace exposure, to dust containing crystalline silica can lead to an increased risk of lung cancer. The evidence suggests that an increased risk of lung cancer is likely to occur only in those workers who have developed silicosis.Disclaimer: The Information in this Safety Advisory Document was obtained from sources which we believe are reliable, but no warranty or representation as to its accuracy or completeness is hereby given. Users should consider the information herein only as a supplement to other information gathered by them and must make independent determinations of suitability and completeness of information from all sources to assure proper use and disposal the safety and health of employees and customers and the protection of the environment.。
Agrilan 1015 A 水溶液可再生溶剂的产品说明说明书
Agrilan® 1015A biodegradable dispersant for aqueous crop protectionformulations2Key benefits• Liquid dispersant• Biodegradable and not persistent, addressing concerns regarding bio accumulative dispersants • No risk or classified ingredients• Emulsifying and wetting agent for water-based formulations, such as EW and SE • Low foamingTypical propertiesAppearance clear liquid CMC 60 mg/l Color< 1 Gardner Density at 20°C 1.06 g/l pH6.0Solid content50%Surface tension at 0.1 wt%32 mN/m Viscosity* at 20°C700 cps*Brookfield DV-III Plus Rheometer; SC-18 spindle @ 25 rpmSuggested SC formulation for Azoxystrobin, Tebuconazole or DiuronIngredient g/L Active 200-300Morwet EFW 20Agrilan 1015*25Ethylene glycol 50Defoamer 1-2Xanthan Gum 1-2Waterup to 1 L*Due to superior wetting of the dispersant, Agrilan 1015 could be used in lieu of the wetting agent (Morwet EFW)Agrilan 1015Agrilan 1015 is a biodegradable dispersant for aqueous crop formulations. It offers a unique patent-protected technology with tapered hydrophobic linking between the hydrophobic and hydrophilic moiety.Regulatory• TSCA and FIFRA approved• Meets REACH polymer exemption• Listed in China and Japanese Chemical InventoryBiodegradability• Biodegradability of Agrilan 1015 as well as a competitor product based on Ethoxylated TSP-phosphate ester (TSP-PE) were evaluated• Continues to biodegrade even after 12 weeks, whereas for TSP biodegradation levels out after three weeks• Can be designated as inherently biodegradable and notpersistent, whereas TSP-PE is nearly non-biodegradable and persistentPercentage of biodegradation of Agrilan 1015 and TSP-PE by activated sludge. The horizontal line represents the percentageachieved upon complete degradation of propylene glycol.B i o d e g r a d a t i o n , %3Diuron 300 g/L SCSome particle size growth upon storage but under better control with Agrilan 1015.• Overall viscosity profile for both SC’s are similar (low to moderate viscosity)• Similar suspensibility (~90%) at RT but Agrilan 1015 is more favorable upon storageBiodegradable liquid dispersant Agrilan 1015 works either as well or better than benchmarkGuideline recipesAzoxystrobin 250 g/L SC Ingredient g/L Azoxystrobin 250Agrilan 101540Mono ethylene glycol 30Biocide 2Defoamer 2Xanthan Gum 2Waterup to 1 LPhysical appearance off-white suspension Particle size, d98, μm 3.5Suspensibilityca 100%Stability, 0°C after 1 week no bleeding Stability, 54°C after 2 weekstrace bleedingProchloraz 250 g/L EW Ingredient g/L Prochloraz 250Agrilan 101530Berol 90430Solvesso 200200Defoamer1Mono ethylene glycol 50Xanthan Gum 1.6DI w aterup to 1 LPhysical appearance white liquid pH (5% in water)7.7Density, g/L, at 25°C 1.086Emulsion stability (342 ppm)stable (2 hrs)Viscosity, cP, 30 rpm, S62, 25°C 520Stability, 0°C after 1 week stable Stability, 54°C after 2 weeksstable90858075Agrilan 1015Benchmark% S u s p e n s i b i l i t y800400200Agrilan 1015BenchmarkV i s c o s i t y , c p s @2.5 r p m6008420Benchmark (TSP derivative)Initial particle size P a r t i c l e s i z e , μm6Agrilan 10157315Nouryon is a global, specialty chemicals leader. Markets and consumers worldwide rely on our essential solutions to manufacture everyday products, such as personal care, cleaning goods, paints and coatings, agriculture and food, pharmaceuticals, and building products. Furthermore, the dedication of more than 7,900 employees with a shared commitment to our customers, business growth, safety, sustainability and innovation has resulted in a consistentlystrong financial performance. We operate in over 80 countries around the world with a portfolio of industry-leading brands. Visit our website and follow us @Nouryon and on LinkedIn.All information concerning our products and/or all suggestions for handling and use contained herein (including formulation and toxicity information) are offered in good faith and are believed to be reliable. However, Nouryon makes no warranty express or implied (i) as to the accuracy or sufficiency of such information and/or suggestions, (ii) as to any product’s merchantability or fitness for a particular use or (iii) that any suggested use (including use in any formulation) will not infringe any patent. Nothing contained herein shall be construed as granting or extending any license under any patent. The user must determine for itself by preliminary tests or otherwise the suitability of any product and of any information contained herein (including but not limited to formulation and toxicity information) for the user’s purpose. The safety of any formulations described herein has not been established. The suitability and safety of a formulation should be confirmed in all respects by the user prior to use. The information contained herein supersedes all previously issued bulletins on the subject matter covered.Products mentioned are trademarks of Nouryon and registered in many countries.D e c e m b e r 2023Contact us directly for detailed product information and sample requestwebsite | /markets/agriculture email|****************BiodegradableAnd non-persistentLiquid dispersantFor crop protection, including seed treatment formulationsLow toxicityNo classified ingredientsEmulsifier and wetting agentFor SEs and EWs, low foam。
waters液相色谱质谱联用的原理应用课件ppt
影响分子量测定的因素
1)pH的影响:正离子方式 pH要低些,负离子方式pH要高些,
除对离子化有影响外,还影响LC的峰形。 2)气流和温度:当水含量高及流量大时要相应增加。 3)溶剂和缓冲液流量:流速适当高可以提高出峰的灵敏度。 4)溶剂和缓冲液的类型:通常正离子用甲醇好,负离子乙腈 好些 5)选择合适的液相色谱类型:正相、反相、选择合适的色谱 柱 6)合适的电压:DP电压高时,样品在源内分解或碎裂;高 DP 电压时回使多电荷离子比例低,多聚体也减少 7)样品结构和性质 8)杂质的影响:溶剂的纯度、水的纯净程度等。当成分复杂, 杂质太多时,竞争使被测物离子化不好,同时使LC分离不好 9)样品浓度不够,有时需要浓缩
m/z149, 管路中邻苯二甲酸酯的酸酐, C8H4O3H+,149.0233 m/z 288, 2mm 离心管的产生的特征离子
m/z 279, 管路中邻苯二甲酸二丁酯 C16H22O4H+, 279.1591
m/z 316, 2mm 离心管的产生的特征离子 m/z 384, 瓶的光稳定剂产生的离子
d) 样品浓度不够
e)pH值不合适 f)样品在源内分解或碎裂
目标化合物分析
(1)选择离子监测(SIM)
SIM 用于检测已知或目标化合物,比全扫 描方式能得到更高的灵敏度。这种数据采集的 方式一般用在定量目标化合物之前,而且往往 需要已知化合物的性质。 若几种目标化合物用同样的数据采集方式 监测,那么可以同时测定几种离子.
m/z391, 管路中邻苯二甲酸二辛酯, C24H38O4H+, 391.2843
m/z413, 邻苯二甲酸二辛酯+钠, C24H38O4Na+, 413.2668 m/z 538, 乙酸+氧 +铁(喷雾管), Fe3O(O2CCH3)6,
液相色谱原子荧光联用仪测定饲料中的无机砷
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spec 常用命令说明书
Basic spec commands for a diffraction experimentDonald A.WalkoBeamline7ID,Advanced Photon Source,Argonne National Laboratory,Argonne,IL60439***************January18,2016AbstractThis document lists some common commands(plus a few other hints)for casual users of the diffrac-tometer control program spec.This is meant to briefly list common ways to use some of the most usefulcommands,not to be an exhaustive list nor a complete description of a command’s syntax.Refer to thespec manual or helpfiles for additional information[1],such as the structure of datafiles,setting motorpositions or software limits,plotting and printing scans,and geometry-specific macros.The beamlinestaffmay also be able to help with these issues,and probably should be consulted before users makesignificant changes such as resetting a motor’s position or soft limits.Starting SPECFrom your local beamline contact,determine how to log in to the appropriate computer to run spec, open any xterminal that may be necessary,and start the spec program.Typically,the program name is the geometry name,such as fourc,kappa,or psic.The basic SPEC commandsspec is a command-line based program.Therefore it is important to know the correct commands; fortunately,some commands will list the type of parameters needed if you enter the wrong type(or number) of parameters.Actually,most“commands”(and many variables)are actually macros and could be redefined, which is not something one should normally do.But the writing and implementation of new macros is quite straightforward;users often write shortcut macros which are combinations of a number of commands.It is also important to note that spec is case-sensitive;most commands and variable names are lower-case,while certain special variables and macros are upper-case.“Information”commandspaI still don’t know if this stands for“parameters”or“print all,”but it is a very useful way to listparameters such as the orientation matrix,lattice parameters,operating mode,wavelength,etc.whwhere;lists positions of the diffractometer motors(in user units;see below),reciprocal lattice coordi-nates,and some relevant angles.wawhere all;lists positions of all the spec motors(in user and dial units;see below).wm motor name(s)where motor;lists where the motor is(user and dial units)and its software limits.lm[motor name(s)]limits;same as wm,except lm will list all motors if none are specified.1p some expressionprint;can be used to print a variable’s value:p F CHIor as a calculator:p5*sin(PI/4)helpcalls the spec help utility,and lists a sizable number of topics which are described to varying degrees of detail.The following commands may be more helpful for advanced users:prdef macro nameprint definition;prints the definition of a macro.lsdeflist defined;lists the names and sizes of all currently defined macros.lscmdlist command;lists built-in commands and functions.whats somethingidentifies an object,as keyword,function,macro,or variablesyms[name]list of known symbols:all or only those which match name(you may use the wildcard characters*or )Miscellaneous commandsct[time]counts and lists results for all scalers.The counting is for time sec or for the default time if value is omitted(such as1sec).But if value is negative,then counting continues until the monitor reaches value counts.Examples of use:ctct10ct-200000The monitor is typically a scaler keeping track of the incident beam.sleep(time)pauses for time eful,e.g.,if you want walk over to a motor to watch it move.Example:sleep(10);umvr th2startupinitializes a variety of parameters.Includes the following macros,which could also be called directly: newsample:title for scan headersnewfile:begins a new datafilesetscans:sets a few scan optionssetplot[value]:options for plotting.Each option has a number,so you can add them up and include value as a shortcut,once you know which options you want.startgeo:calls geometry-dependent set-up macrosdo commandfilereads commands from a textfile.It’s usually good form for thefile name to have a.mac extension qdo commandfilequiet do;same as do,but doesn’t print the commands to the screen.save[file name]saves numerous parameters to a textfile.Allows you to recover things like the orientation matrix if you want to make temporary e the do or qdo command to read thefile back into spec.2comment"whatever you want to say"writes a time-stamped comment to the datafile.u[unix command]unix shell:executes unix command(if included)or goes to the unix command line.To escape from the unix command line,type exit.Some unix commands are directly accessible without typing the u: cd:change directoryls:list directory contentsl:list directory contents(the unix ls-l command)pwd:present working directoryquitquit out of spec.“exit”does not do this.Be careful to understand the effects of the following commands before executing them.They may,for example,be safe on a simple rotary stage,but not on a more complex diffractometer:set motor name positionsets a motor’s position(in user units).set lm motor name low highsets a motor’s limits(in user units).set dial motor name positionsets a motor’s position(in dial units).configcalls the hardware configuration editor.Allows configuration of motors,scalers,and other devices.These are mostly advanced options which should not be altered casually.Simple motor motionsumv motor name positionmove motor name to absolute position(in user units).Examples:umv th20umv th CENSee below under dscan for information on the variable CEN.umvr motor name rel positionmove motor name by the relative amount rel position from its current position.ubr H K Lmove motors to the reciprocal lattice point(Bragg point)defined by the Miller indices H K Lca H K Lcalculate the motor position for the reciprocal lattice point H K L.It’s a good habit to do ca before ubr,to avoid unexpected motor motions.tw motor name deltatweak;interactive subroutine to move motor name by delta.Once in the subroutine,each time you hit Enter the motor moves by delta.You can change direction with p/n or+/-,and also change delta by entering a new value.Escape by hitting CTRL-C,or some other letter or symbol,followed by Enter.The‘u’in umv,umvr,and ubr stands for‘update;’the motor positions are regularly updated on the screen while they move.This is not required,but is preferable to mv,mvr,and br since it is not obvious from the latter commands when the motion is completed:spec may appear to have hung,since the prompt appears but won’t respond to new commands until the motors are done moving.3Basic scansA main use of spec is to scan motors and collect data.If you are ever unsure of the order of parameters for a certain scan,just type the scan name and spec will list the parameters in order.For all these scans,one enters the number of intervals,which is one more than the number of points. Thus,the step size is(ending point)-(starting point)/intervals.The unit of time is seconds per point if positive,or monitor counts per point if negative.loopscan npts[count time[sleep time]]time-lapse scan:sit at current conditions and count for npts points without moving motors timescan[count time[sleep time]]indefinite time-lapse scan,i.e.,a loopscan with npts=0Motor scansascan motor name start end intervals timeabsolute scan:motor name starts at start and ends at end(in user units).At the end of the scan, motor name stays at end.Example:ascan th57301dscan motor name rel start rel end intervals timerelative(differential)scan:motor name starts at start+current position and ends at end+cur-rent position.At the end of the scan,motor name returns to its previous position.This is the same as a lup(line up)scan.Example:dscan th-11301;umv th CENThe variable CEN(all caps)is calculated after each scan,and is the absolute position of the peak’s center(as given by the FWHM,not the highest position or the center-of-mass).As long as there is a peak in the scan,this is a good way to line up to it.Note that if you typed umvr th CEN or umv phi CEN you could get into big trouble!It may also give weird results if the FWHM couldn’t be calculated from the scan(e.g.,because of a background value higher than50%of the peak value).a2scan motor name1start1end1motor name2start2end2intervals timeabsolute scan of two motors:motor name1starts at start1and ends at end1,while motor name2 starts at start2and ends at end2.a3scan and a4scan operate similarly,d2scan,d3scan,and d4scan are multimotor relative scans.mesh motor name1start1end1intervals1motor name2start2end2intervals2timemotor mesh scan.A scan of motor name1is done for each point of motor name2,all of which is stored as one spec scan.Example:mesh th5750tth1014301In this example,the full scan contains51*31=1581points.resume[n]resumes an aborted scan.If a positive integer n is included,then n points are skipped.If a negative integer is included,then the last n points are repeated.Reciprocal space scanshscan h start h end intervals timelinear scan in reciprocal space along the H axis.The values of K and L during this scan are based on the previous position in reciprocal space,so you may need to use the ubr command tofirst move to the appropriate point.Example:ubr111;hscan.9 1.120-20000kscan k start k end intervals timesame as hscan but along the K axis.lscan l start l end intervals timesame as hscan but along the L axis.4hklscan h start h end k start k end l start l end intervals timelinear scan in reciprocal space along a general direction.For example,if you wanted to scan in some direction along H and K thru the(111)Bragg peak:hklscan.9 1.1 1.20.811201hklmesh Q1start1end1intervals1Q2start2end2intervals2timereciprocal space mesh scan.Q1and Q2are literally H,K,or L.Thus this type of mesh scan is limited to be along the principal axes of reciprocal space.The value of the third reciprocal space coordinate during this scan is based on the previous position in reciprocal space,so you may need to move there first.For example,if you wanted to scan in the H-L plane thru the(111)Bragg peak:ubr.81.9;hklmesh H.8 1.220L.9 1.1201More complicated scans in reciprocal space(e.g.,radially,or along circles)are possible.See the spec manual for details[1].The orientation matrix and other issuesAn important function of spec is as a calculator,for the transformation between diffractometer angles and reciprocal lattice coordinates.The most important aspect of this is the orientation matrix,i.e.,the angular position of the crystal lattice.The basic commands for setting up an orientation matrix are given here,but see the spec manual[1]or your beamline contact for additional information.The orientation matrix is set byfinding two nonparallel Bragg reflections.Since the orientation matrix is never perfect,the primary reflection will exactly agree with the orientation matrix(to a scale factor), but the secondary reflection will not exactly e the commands or0and or1to set the primary and secondary reflections,respectively,if the diffractometer is at the reflection,or use setor0and setor1if you know the appropriate angles but the diffractometer is at some other location.The lattice parameters are set with the setlat command,and the x-ray wavelength is given by the value of the variable LAMBDA.There are three other aspects of determining a unique set of angles for a given(HKL)Bragg point.These vary depending on the particular spec geometry,so are only briefly mentioned here:modes there are generally more diffractometer angles than there are dimensions in reciprocal space(i.e.,3);additional constraint(s)is/are set via the selection of a mode(e.g.,constraining the angle of incidence, or constraining the position of a particular motor).sectors this is how spec selects between sets of angles that are geometrically equivalent.For example,the angle pair(twotheta,omega)is equivalent to(-twotheta,180-omega),but usually one prefers positive values of twotheta.cut points this determines how to break the360◦degeneracy of the circles to avoid wraparound situations.For example,suppose the phi cut point is-180◦,phi is currently at-175◦,and you want to move to -185◦.Then the phi motor will not make a-10◦move but will in fact make a+350◦move to+175◦. User units vs.dial unitsspec maintains an important distinction between the“user units”and“dial units”of a motor.The dial units are the actual values which are read on a motor’s physical dial(when such a dial exists).spec keeps track of a motor’s position using the dial units(for example,in calculating whether a given motion would violate a software limit).Dial units are algebraically converted to user units,which are the units spec uses in calculations such as reciprocal lattice coordinates.As an example,if the detector is positioned to intercept the direct beam but the tick mark on the dial points to90,then tth=0in user units but90in dial units.If you become concerned that a motor has somehow lost its position,you can go into the hutch and read the number offthe dial(if it exists)to compare with the dial units listed in spec.CountersData are recorded by spec via counters(also called scalers).Little will be said here,since so much depends on the particular hardware.Two special scalers are set in the configfile,the timebase(units of seconds)and the monitor.A“ct n”command will count to the timebase if n is positive or to the monitor5if n is negative.Thus,monitor is typically a counter for the incident beam to normalize the signal to the incidentflux.Unfortunately,there is another convention wherein one scaler is called DET and another is called MON; these can be set by giving values to these variables(e.g.,DET=2)or by the command counters.MON is not necessarily the same as the monitor defined above,but I think these counters occupy special columns in the spec datafile.Finally,the relatively new command plotselect lets you choose which counter(s)are plotted on the screen during a scan.References[1]The Certified Scientific Software website has an online manual and help pages for spec at6。
ATP Assay Kit (Colorimetric Fluorometric)说明书
Product nameATP Assay Kit (Colorimetric/Fluorometric)Detection methodColorimetric/Fluorometric Sample typeUrine, Serum, Plasma, Other biological fluids, Tissue Extracts, Cell Lysate Assay typeQuantitative Sensitivity< 1 µM Assay time1h 00m Product overview ATP Assay Kit (Colorimetric/Fluorometric) (ab83355) use a robust, simple method; the ATPassay protocol relies on the phosphorylation of glycerol to generate a product that is easilyquantified by colorimetric (ODmax = 570 nm) or fluorometric (Ex/Em = 535/587 nm) methods.This kit can detect as low as 1 µM of ATP in various samples.ATP assay protocol summary:- add samples (deproteinized) and standards to wells- add reaction mix and incubate for 30 min at room temp- analyze with microplate readerChinese protocol available. See protocols section below.If you require a more sensitive product, we recommend Luminescent ATP Detection Assay Kit (ab113849), which can detect as low as 1 pM of ATP.Notes This product is manufactured by BioVision, an Abcam company and was previously called K354ATP Colorimetric/Fluorometric Assay Kit. K354-100 is the same size as the 100 test size ofab83355.Related assaysReview the cell health assay guide to learn about kits to perform a cell viability assay , cytotoxicity assay and cell proliferation assay .Review the metabolism assay guide to learn about assays for metabolites, metabolic enzymes,mitochondrial function, and oxidative stress, and also about how to assay metabolic function inlive cells using your plate reader.How other researchers have used ATP Assay Kit ab83355Product datasheetATP Assay Kit (Colorimetric/Fluorometric) ab833555 Abreviews 373 References 8 Images OverviewThis ATP assay kit has been used in publications in a variety of sample types, including:- Human: cell culture lysates , primary monocyte cell culture lysates , HCT116 cell culturesupernatants - Mouse: heart tissue , liver , C2C12 and L929 cell lysates , primary thymocyte cell culturelysates , cardiac tissue - Rat: primary hippocampal neuron cell culture lysates , liver tissue , skeletal muscle - Pig: kidney cell culture lysates , heart tissue- C elegans tissue - Chlamydomonas reinhardtii algaePlatform Microplate readerStorage instructionsStore at -20°C. Please refer to protocols.PropertiesComponentsIdentifier 100 tests 2000 tests Assay Buffer XXIIIWM 1 x 25ml 20 x 25ml ATP Converter (lyophilized)Blue 1 vial 20 vials ATP Probe (in DMSO)Red 1 x 200µl 20 x 200µl ATP Standard (1 µmol; lyophilized)Yellow 1 vial 20 vials Developer Mix (lyophilized)Green 1 vial 20 vialsImages123456789101112131415References: 1 - Civallero M et al 2017, Na JY et al 2018, 2Gkirtzimanaki K et al 2018, 3Y ang et al 2018; 4 - Singh SP et al2018; 5 - Han SJ et al 2018; 6 - A lhindi Y et al 2019, Gregorczyk KP et al 2018; 7 - Simula L et al 2018; 8 - Litt M J et al 2017,Samokhvalov V et al 2018; 9 - Zhao X et al 2018; 10 - Jing R et al 2018; 11 - Trinchese G et al 2018; 12 - Zou X et al 2018;13 - Y uan F et al 2018; 14 - Pandey et al 2018; 15 - Ramanan R et al 2018ATP lev els in Pancreatic Islet Image courtesy of M rs. Fotini M outh Ab83355 was used to determin ATP levels in rat pancreas islets as an ischemic marker to predict transplantation outcomes. We extracted ATP from fresh pancreas that have undergo different time of cold ischemia : 0, 2, 4, 6, 8 and 10h and in situ. ATP were extracted in Perchloric acid (PCA-2M) and grind using a Polytron. PCA were removed using potassium hydroxide (KOH – 2M) and pH was adjust around 7-8. Samples were conserved at -80°C before utilization.ATP assay used to study mitochondrial disfunction after C. rodentium infection in miceImage courtesy of M aiti A K et al. PLoS One. 2018;13(9): e0204567. doi: 10.1371/journal.pone.0204567Maiti AK et al (2018) used ATP assay kit ab83355 to measure mitochondrial ATP generation in an i n vitro mouse intestinal model treated with cytokines in the presence and absence of VIP (vasoactive intestinal peptide). VIP was induced by C. rodentium infection and cytokines.ATP assay performed with ab83355Sanokawa-A kakura R et al., PLoS One 9(9), fig4b. doi: 10.1371/journal.pone.0108537 Reproduced under the Creative Commons license/licenses/by/4.0/The chart shows a comparison of ATP levels of HepG2 treated with 0, 10 and 100 µM for 48 hours, DR(damage recovered cells using hydrogen peroxide with a recovery time of one week) HepG2 cells and MDA-MB-231 cells treated with 0, 10 and 100 µM of NaHS for 48 hours. Data is shown as percent of ATP levels in untreated cells. ATP levels were determined using ATP assay kit (ab83355).ATP assay performed with ab83355Image from Shi Z et al., PLoS One 9(8), Fig 2 doi: 10.1371/journal.pone.0105675. Reproduced under the Creative Commons license/licenses/by/4.0/MCF-7 cells are transfected with vector, osteopontin-a, osteopontin-c or osteopontin -a plus -c. Cells are plated on poly-HEMA and seeded at 4 x 10cells per well and incubated for two days under standard culture conditions. ATP levels are measured using ATP assay kit (ab83355).ATP assay performed with ab83355Example of fluorometric ATP assay standard curve.H2O2 W15ATP lev els measured in mouse colon tissue Image courtesy of M aiti A K et al. Sci Rep. 2015; 5: 1543. doi: 10.1038/srep15434. Reproduced under the Creative Commons License/licenses/by/4.0/Maiti AK et al. (2015) used ATP assay kit ab113852 to measure mitochondrial ATP generation in murine distal colon after C. rodentium infection.ATP assay performed with ab83355Example of colorimetric ATP assay standard curve.ATP assay performed with ab83355Quantitation of ATP in fish liver (2.5µl of 10 times diluted sample), fish muscle (5µl of 10 times diluted sample) and Jurkat cell lysate (5 ul) using fluorometric assay. Samples were spiked with known amounts of ATP (300pmol).Please note: A ll products are "FOR RESEA RCH USE ONLY. NOT FOR USE IN DIA GNOSTIC PROCEDURES"Our Abpromise to you: Quality guaranteed and expert technical support Replacement or refund for products not performing as stated on the datasheetValid for 12 months from date of deliveryResponse to your inquiry within 24 hoursWe provide support in Chinese, English, French, German, Japanese and SpanishExtensive multi-media technical resources to help youWe investigate all quality concerns to ensure our products perform to the highest standardsIf the product does not perform as described on this datasheet, we will offer a refund or replacement. For full details of the Abpromise, please visit https:///abpromise or contact our technical team.Terms and conditionsGuarantee only valid for products bought direct from Abcam or one of our authorized distributors。
马特瑞克无水氨说明书
Section 1: Chemical Product and Company InformationProduct name: Anhydrous AmmoniaSupplier/ Further Information: Martrex, Inc. Web: !P . O. Box 1709!Phone: 952/933-5000!14525 Highway 7 !Toll Free: 800/328-3627!Minnetonka, Minnesota 55345-3793 !FAX: 952/933-1889EPA Registration Number: n/aCAS#: 7664-41-7Chemical Name: Anhydrous Ammonia Synonyms: Ammonia, Ammonia Gas Chemical Family: AmmoniaMSDS Number: n/a24 Hour Emergency Phone - Chemtrec Transport: 1-800-424-9300; Medical: 1-800-441-3637 Section 2: Composition/Information on IngredientsHazardous ComponentCAS#%OSHA PEL OSHA STEL OSHA CEIL Ammonia 7664-41-799%+50ppm(35mg/m 3)n/a n/a OTHER LIMITS RTECS#ACGIH TLV ACGIH STEL ACGIH CEIL See Section 15n/a25ppm(17 mg/m 3)35ppm(24mg/m 3)n/a Non-Hazardous Component CAS#%Water trace Section 3: Hazards IdentificationEmergency Overview: Stay upwind. Isolate the release area and deny entry. Evaluate the affected areas todetermine whether to evacuate or shelter in place. Anhydrous ammonia causes severe eye injury, severe damage to lungs and respiratory system, and severe skin damage. Harmful or fatal if swallowed or inhaled. This product is acutely toxic by inhalation as defined by OSHA. This product is classified as an Inhalation Hazard (DOT) and can cause chemical burns. If spilled into a waterway, ammonia can be toxic to aquatic life and may cause eutrophication. See NAERG, Guide 125.NFPA: Health: 3 Flammability: 1 Reactivity: 1Potential Health Effects:Primary Routes of Exposure / Entry: Inhalation (breathing), eye contact,skin contact. (Ingestion is unlikely, ammonia exists as a gas at normalatmospheric conditions.)Target Organs: Anhydrous ammonia has acute effects on the respiratorytract, lungs, eyes, and skin. There is also limited evidence reported ofkidney damage from prolonged exposure to elevated concentrations.Acute Exposure SymptomsInhalation: Ammonia gas causes varying degrees of irritation and damage based on the concentration andduration of exposure. The severity of damage from exposure to ammonia vapors is proportional to theexposure concentration and duration. Immediate, mild irritation of the respiratory tract can occur at con-Material Safety Data SheetHealthFire Reactivity SpecialHazard For Rating Explanation see Section 16 113centrations exceeding 50-100 ppm ammonia. Severe irritation of the respiratory tract can occur at con-centrations exceeding 400-700 ppm ammonia. Exposure to concentrations exceeding 4000-5000 ppm can be rapidly fatal. Exposure can cause immediate and delayed effects.Eye Contact: The severity of damage from exposure to ammonia vapors is proportional to the exposure concentration and duration. Mild eye irritation can occur at ammonia concentrations exceeding 50- 100 ppm. Severe eye irritation can occur at ammonia concentrations exceeding 400 ppm. Exposure to con-centrations of ammonia vapor above 1000 ppm and/or liquid ammonia may result in permanent damage to the eye resulting in temporary or permanent blindness. Aqueous ammonia rapidly penetrates ocular tissue and may cause permanent damage.Skin Contact: The severity of damage from exposure to ammonia vapors is proportional to the exposure concentration and duration. Splashes of liquid ammonia can cause severe damage to the skin. Ammonia is corrosive to the skin..Ingestion: Ingestion will result in severe damage to the gastro-intestinal tract.Chronic Exposure SymptomsInhalation:Chronic inhalation of concentrations that exceed recommended or regulatory levels may result in immediate and delayed lung irritation and injury. There is also limited evidence reported of kidney dam-age from prolonged exposure to elevated concentrations.Medical Conditions Aggravated By Long-Term Exposure: Existing skin disorders and lung disorders (such as asthma) may be aggravated by long-term exposure.Section 4: First Aid MeasuresInhalation:Remove from area of exposure immediately. GET MEDICAL ATTENTION IMMEDIATELY. Exposure to ammonia vapor causes both immediate and delayed effects, which may be serious. See Section 3.Eye Exposure: Wash eyes IMMEDIATELY and thoroughly (for 30 minutes). Hold eyelids apart to ensure com-plete irrigation of all eye and eyelid tissues. GET MEDICAL ATTENTION IMMEDIATELY.Skin Exposure: Flush skin immediately and thoroughly (for 20 minutes), while removing contaminated clothing.GET MEDICAL ATTENTION IMMEDIATELY.Ingestion: Drink large amounts of water, DO NOT INDUCE VOMITING. NEVER give anything by mouth to an unconscious person. GET MEDICAL ATTENTION IMMEDIATELY.NOTE TO THE PHYSICIAN: Pneumonitis should be anticipated after inhalation or ingestion. If severe exposure is suspected, observe for 48-72 hours for delayed pulmonary edema. Do not apply salves or ointments for first 24 hours.Section 5: Fire Fighting MeasuresFlammability Classification:NFPA= 1HMIS = 1DOT= Nonflammable GasFlash Point: Not ApplicableAuto-ignition Temperature: 1204ºFLower explosion limit (LEL): 16% by volume, in airUpper explosion limit (UEL): 25% by VOlume, in airExtinguishing Media: Use water fog or spray.Unusual Fire and Explosive Hazards: Airborne concentrations between 16-25% can explode when ex-posed to an ignition source. See Section 10 for Chemical Incompatibilities.Hazardous Decomposition Materials: Nitrogen oxides, hydrogenSpecial Procedures:Fire-Fighting Instructions: Stopping the flow of gas is recommended when escaping gas is ignited, rather than extinguishing the fire. Use water spray to allow personnel access to shut off valves. Keep containers cool by application of water spray. Do not put water on liquid ammonia. Mixing of liquid ammonia and water will gen-erate heat and vapors. Do not release runoff from fire control methods to sewers or waterways. SeeNAERG, Guide 125.Personal Protective Equipment: Because of ammonia presence and the potential that the fire may produce toxic decomposition products, wear chemical resistant suit, gloves, boots, and a self-contained breathing apparatus (SCBA) with a full face piece operated in positive-pressure mode. Suits must be rated for use with anhydrous ammonia.CAUTION:Normal fire fighting gear does not provide adequate protection. Liquid ammonia can cause PPE to become brittle and crack.Section 6: Accidental Release MeasuresSpill and Leak Procedures: Wear chemical resistant suit, gloves, and boots or a fully encapsulated suit rated for use with anhydrous ammonia, based on spill/leak volume and conditions. Wear a self-contained breath-ing apparatus (SCBA) with a full face piece. Stop the leak if possible. Use water spray to control vapors. See Section 10 for Chemical Incompatibilities.Containment of Spill: SMALL SPILLS: Use water spray to control vapors. Dilute with water. Do not release into sewers or waterways. LARGE SPILLS: Place dirt berms or other barriers down gradient to prevent loss into sewers or waterways. DO NOT USE MOBILE EQUIPMENT OR INTRODUCE A POTENTIAL IGNITION SOURCE IN AREAS OF AMMONIA VAPOR CONCENTRATIONS BETWEEN LEL & UEL. Use water fog or spray to absorb ammonia vapors.Cleanup and Disposal of Spill: Recovery of liquid ammonia should only be conducted by highly trained per-sonnel.Environmental and Regulatory Reporting: Follow applicable OSHA regulations (29 CFR 1910.120) to protect workers during cleanup. See Section 15 for additional regulatory requirements. Additional information is available in the NAERG, Guide 125.Section 7: Handling and StorageMinimum/maximum Storage Temperature: Protect storage containers from excessive temperatures. Handling: Wear splash proof chemical goggles, ammonia resistant gloves, and protective clothing as a mini-mum while handling ammonia. Additional full-face protection is recommended. Respiratory selection should be based on known or anticipated exposure levels. See Section 8 for additional information. CAUTION: Liq-uid ammonia can cause PPE to become brittle and crack.Storage: Protect storage containers from impact and excessive temperatures. Use only system components and containers rated for use with anhydrous ammonia. Zinc, copper, silver, cadmium, and their alloys should not be used in ammonia systems due to their potential for rapid corrosion when exposed to ammonia. Stor-age systems must have adequate pressure relief valves. Refer to the current ANSI K61.1 Standard, Safety Requirements for the Storage and Handling of Anhydrous Ammonia for additional information.Shelf Life: IndefiniteREGULATORY REQUIREMENTS: See Section 8 for employee exposure controls and Section 15 for other regulatory requirements.Section 8: Exposure Controls / Personal ProtectionVentilation Protection: Provide general or local exhaust ventilation systems or other engineering controls to maintain airborne concentrations below regulatory levels (See Section 15).Respiratory Protection (specify type):If concentrations exceed recommended exposure levels, use a NIOSH-approved ammonia vapor respirator suitable for the exposure conditions (as a minimum level of protection).Seek professional advice prior to respirator selection and use. Follow OSHA respirator regulations (29 CFR 1910.134). Select respirator based on its suitability to provide adequate worker protection for given working conditions, level of airborne contamination, and presence of sufficient oxygen. WARNING! AIR-PURIFYING RESPIRATORS DO NOT PROTECT WORKERS IN OXYGEN DEFICIENT ATMOSPHERES. If respirators are required, OSHA requires a written respiratory protection program that includes at least: medical certifica-tion, training, fit-testing, periodic environmental monitoring, maintenance, inspection, cleaning, and conven-ient, sanitary storage areas.Eye Protection: Wear protective splash proof safety goggles and face protection, per OSHA eye- and face pro-tection regulations (29 CFR 1910.133). Contact lenses should not be worn while handling anhydrous am-monia.Skin Protection: Wear chemical resistant gloves and boots (such as neoprene or rubber) and appropriate chemical resistant clothing to prevent skin contact.Other Protective Clothing and Equipment: SAFETY STATIONS: Make emergency eyewash stations and showers available in the immediate work area. Agricultural distribution requires shower and/or > 100 gallons fresh water in open top container. Field transportation requires >5 gallons of fresh water.Hygienic Work Practices: Decontaminate and air dry all contaminated personal protective equipment prior to storage and inspection for possible reuse. Separate heavily contaminated work clothes fromstreet clothes. Launder before reuse. COMMENTS: Practice good personal hygiene during and afteruse of this material, especially before eating, drinking, smoking, using the toilet, or applying cosmet-ics.Section 9: Physical and Chemical PropertiesChemical Name: Anhydrous AmmoniaPhysical State: Gas under atmospheric conditions, liquid under pressureColor and Appearance: Colorless gas or clear liquid.Odor: Sharp, irritating, pungent odor.Odor Threshold: 25 ppm (in air)pH (in water): 11.6 (1 N), 11.1 (0.1 N), 10.6 (0.01N)Specific Gravity: n/aVapor Pressure, 8.5 atm @ 20ºCVapor Density: (Air=1): 0.5967Density: Gas=0.7710 g/L; Liq=0.6818 g/L(-33.4ºC/1 atm)Volatiles by Volume: 100%Boiling Point: -33.35ºCSoftening Point: n/aMelting Point: -77.7ºCEvaporation Rate: n/aSolubility in water 42.8% (0ºC) Hydroscopic materialOther Solubilities: Soluble in alcohol, ether, organic solventsChemical Formula: NH3Formula Wt: 17.03Section 10: Stability and ReactivityChemical Stability: Stable X UnstableHazardous Polymerization: May OccurWill Not Occur XConditions to Avoid: Exposure to elevated temperatures and fire.Chemical Incompatibility: Strong acids, oxidizing gases. Under certain conditions ammonia reacts with chlo-rine, bromine, fluorine, or iodine (halogens) to form compounds that explode spontaneously. May form ex-plosive compounds on contact with gold, silver, mercury, or hypochlorite. Reacts with copper, copper alloys, aluminum alloys, and galvanized surfaces.Hazardous Decomposition Products: Nitrogen oxides, hydrogen.Section 11: Toxicological InformationAcute DataEye Effects: 100-200 ppm -- moderate to severe200-1000 ppm -- eye damageSkin Effects: Liquid Ammonia = severe burnsAmmonia Vapor = mild to severe irritation, relative to exposure concentration & durationOral LD50: No data (Not a likely route of exposure.)Dermal LD50: no dataInhalation LC50(rat): 4230 - 19960 mg/m3/1-hr ; This product has been determined to be acutely toxic per the criteria of OSHA 1910.1200, Appendix A.Skin Sensitization: no dataChronic DataChronic Effects: See Section 3Chronic Toxicity Studies: no dataMutagenicity Data: no dataReproductive and Teratological Data: no dataCarcinogenicity Data: See Section 3. 'See NIOSH, RTECS BO 0875000 for additional information.NTP: no data OSHA: no data IARC Monograph: no data Not Listed:Section 12: Ecological InformationEco-acute Toxicity: Ammonia in elevated concentrations can cause vegetation kill and contribute to eutrophica-tion. Ammonia has been determined to be slightly toxic to aquatic organisms per USEPA criteria. Environmental Fate: Ammonia is a naturally occurring compound. Ammonia in soil can be rapidly transformed to nitrate by the microbial population through nitrification. The nitrate form will either leach through the soil or be taken up by plants or other organisms. In water ammonia can undergo sequential transformation by two processes in the nitrogen cycle, nitrification and denitrification, which would produce ionic nitrogen com-pounds, and from these, elemental nitrogen.Section 13: Disposal ConsiderationsDisposal Procedures: Contact federal or state regulatory agencies for acceptable disposal/use of the recov-ered materials. Ammonia contaminated water from vapor control may be suitable for use as fertilizer or may need to be sent to a waste treatment facility.Disposal Regulatory Requirements: Follow applicable Federal, state, and local regulations if disposal is nec-essary.Container Cleaning And Disposal: Not applicable.Section 14: Transport InformationDOT Transportation Data (49 CFR 172.101):Proper Shipping Name: Ammonia, anhydrousHazard Class: 2.2ID NO.: UN1005Packing Group: n/aLABEL: Nonflammable Gas with "Inhalation Hazard" marking (See 172.102, Special Provision 13)PLACARD: Nonflammable Gas with "Inhalation Hazard" marking (See 172.102, Special Provision 13) Section 15: Regulatory InformationEPA Regulations:RCRA Hazardous Waste Number (40 CFR 261.33): Not listedCERCLA Hazardous Substance (40 CFR 302.4): YesCERCLA Reportable Quantity (RQ): 100 lbs.SARA 311/312 Codes: Yes-Acute, Sudden Release of Pressure.SARA Toxic Chemical (40 CFR 372.65): YesSARA EHS (Extremely Hazardous Substance) (40 CFR 355): YesSARA EHS Threshold Planning Quantity (TPQ): 500 Ibs.CAA/RMP (Toxic Substances) (40 CFR 68.130): Yes, Ammonia (anhydrous)CAA/RMP (TQ): 10,000 lbs.OSHA Regulations:AIR CONTAMINANT (29 CFR 1910.1000, Table Z-1, Z-1-A): OSHA, ACGIH, and NIOSH data for ammoniafollows:OSHA: TWA = 50 ppm (35 mg/m3)ACGIH: TWA = 25 ppm (17 mg/m3), STEL = 35 ppm (24 mg/m3)NIOSH: TWA = 25 ppm (18 mg/m3), STEL = 35 ppm (27 mg/m3)IDLH = 300 ppmProcess Safety Management (29 CFR 1910.119): YesThreshold Quantity (TQ): 10,000 Ibs.Storage And Handling Of Anhydrous Ammonia (29 CFR 1910.111): YesState Regulations: This product is regulated in commerce by state agricultural and/or consumer protectionlaws. This product is listed in various state Right-to-know, worker protection, and/or environmental protection laws. If you are unable to determine the proper status of this product under your respective state laws con-tact the manufacturer.Section 16: Other InformationACGIH - American Confer-ence of GovernmentalIndustrial HygienistsANSI - American National Standards Institute CAS - Chemical AbstractsService CERCLA - Comprehensive Environmental Response,Compensation & Liability Act of 1980CFR - Code of Federal Regu-lations CHEMTREC - Chemical Transportation Emer-gency Center CPR - Controlled Products Regulations CWC - Chemical Weapons Convention DOT - U.S. Department of TransportationDSL - Canadian Domestic Substance ListEHS - Extremely Hazardous SubstanceEPA - U.S. Environmental Protection AgencyHMIS - Hazardous Material Identification SystemIARC - International Agency for Research on CancerLEL/UEL - Lower and Upper Explosive Limitmg/m 3 - Milligrams per cubic meterMSDS - Material Safety Data SheetNAERG - North American Emergency Response GuidebookNIOSH - National Institute of Occupational Safety and HealthNFPA - National Fire Protection AssociationNTP - National Toxicology ProgramOSHA - Occupational Safety and Health AdministrationPEL - Permissible Exposure Limit (set by OSHA) Rating Number Health Hazard Flammability Hazard Instability Hazard Special Hazard Rating Symbol Will vaporize and readily burn at normal tem-peratures Can be ignited under almost all ambient tem-peratures Must be heated or high ambient temperature to burn Must be pre-heated before ignition can occur May explode at normal tempera-tures and pres-sures May explode at high temperature or shock Violent chemical change at high temperatures or pressures Normally stable. High tempera-tures make un-stable Will not burn Stable No Hazard Can cause sig-nificant irritation Can cause tem-porary incapaci-tation or residual injury Can cause seri-ous or perma-nent injury Can be lethal Reacts violently or explosively with water Reacts violently or explosively with water or oxidizer 43210W OX W Radioactive OXY COR Oxidizer Strong Corrosive ACID ALK Acidic Alkaline CRYO Cryogenic BIO BioHazard This chart for reference only - For complete specifications consult the NFPA StandardPPE - Personal Protective EquipmentRCRA - Resource Conservation and Recovery Act of 1976RTECS - The Registry of Toxic Effects of Chemical SubstancesSARA - Superfund Amendments and Reauthorization ActSTEL - Concentration to which workers can be exposed continuously for a short period of time without suffering from irritation, irreversible tissue damage or narcosis of sufficient degree to increase the likelihood of acci-dental injury, impair self-rescue or materially reduce work efficiency.TDG (Canadian): Transport of Dangerous Goods RegulationsTLV - Threshold Limit Value (set by ACGIH)TWA - 8-hour Time Weighted AverageTSCA - US Toxic Substance Control ActWHMIS - Workplace Hazardous Material Information SystemMSDS Issue Date: n/aRevised Date: 6-18-2013Supersedes: 5-4-2009Disclaimer: Martrex, Inc. provides the information contained herein in good faith but makes no representation as to its comprehensiveness or accuracy. This document is intended only as a guide to the appropriate precau-tionary handling of the material by a properly trained person using this product. Individuals receiving the in-formation must exercise their independent judgment in determining its appropriateness for a particular pur-pose.MARTREX, INC. MAKES NO REPRESENTATIONS OR WARRANTIES, EITHER EXPRESS OR IMPLIED, IN-CLUDING WITHOUT LIMITATION ANY WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE WITH RESPECT TO THE INFORMATION SET FORTH HEREIN OR THE PRODUCT TO WHICH THE IN-FORMATION REFERS. ACCORDINGLY, MARTREX, INC. WILL NOT BE RESPONSIBLE FOR DAMAGES RESULT-ING FROM USE OF OR RELIANCE UPON THIS INFORMATION.。
SMC 开关设备操作指南说明书
TroubleshootingSpecificationThe IODD file can be downloaded from the SMC website (URL ).Refer to the product catalogue or SMC website (URL ) for more detailed information about product specifications.DimensionsRefer to the product catalogue or SMC website (URL ) for more detailed information about dimensions.than above are displayed, please contact SMC.Error indicationSnap shot functionThe current flow rate/temperature value can be stored to the switch output ON/OFF set point.When the set value and hysteresis are set, press the UP and DOWN buttons for 1 second or longer simultaneously. Then, the set value of the sub display (right) shows [- - -], and then values corresponding to the current flow rate/temperature are automatically displayed.Peak/bottom value indicationThe max. (min.) rate/temperature when the power is supplied is detected and updated.The value can be displayed on the sub display by pressing the UP or DOWN button in measurement mode.Key-lock functionTo set this function, refer to SMC website (URL ) for more detailed information or contact us.MaintenanceHow to reset the product after a power cut or when the power has been unexpectedly removedThe settings of the product are retained from before the power cut or de-energizing.The output condition also recovers to that before the power cut or de-energizing,but may change depending on the operating environment.Therefore, check the safety of the whole system before operating the product.Function selection mode[F Select to display the function to be change [F mode to return to measurement mode.∗: The sub screen displays the content of function and the setting of the function alternately.The function number is increased and decreased by the UP and DOWN buttons.Display the required function number and press the SET button.Default settingsThe default settings are provided as follows. If these settings are acceptable,retain for use. To change setting, refer to SMC website(URL ) for more detailed information or contact us.Display of sub screenIn measurement mode, the display of the sub screen can be temporarily changed by pressing the UP or DOWN buttons.∗: After 30 seconds, it will automatically reset to the display selected in [F10].∗: Arbitrary displayThe set values and accumulated output of OUT2 cannot be displayed.(Example for 16 L/min type the above )The switch turns on within a set flow range (from P1L to P1H) during window comparator mode. Set P1L (switch lower limit) and P1H (switch upper limit) using the setting procedure above.When reversed output is selected, the main screen displays [n1L] and [n1H].To set accumulated output functions, refer to the product catalogue orSMC website (URL ) for more detailed information.For models with 2 outputs, [P_2] or [n_2] will be displayed. Set as above.For models with the temperature sensor attached, [ tn] will be displayed.When the fluid temperature falls below the set value, the output turns ON.∗: If a button operation is not performed for 30 seconds during the change of setting, the set value will start flashing.Refer to the SMC website (URL ) for more detailed information about product troubleshooting.Note: Specifications are subject to change without prior notice and any obligation on the part of the manufacturer.© 2018 SMC Corporation All Rights Reserved Akihabara UDX 15F, 4-14-1, Sotokanda, Chiyoda-ku, Tokyo 101-0021, JAPAN Phone: +81 3-5207-8249 Fax: +81 3-5298-5362URL PF ※※-OMV0007Safety InstructionsFlow (Temperature) SettingInstallationBracket mounting (PF3W704/720/740)Mount the product (with bracket) usingthe mounting screws supplied (M4 x 4 pcs.).For models with flow adjustment valve attached, fix using 8 mounting screws.Bracket thickness is approx. 1.5 mm.Measurement modeThe mode in which the flow is detected and displayed, and the switch function is operating.This is the basic operating mode; other modes should be selected for set-point and other function setting changes.Approx. 3 seconds for this period)Mounting and InstallationInstallation•Use the product within the specified operating pressure range and temperature range.•Proof pressure could vary according to the fluid temperature.Check the characteristics data for operating pressure and proof pressure.(4 pins) (Option)(Option)Direct mounting (PF3W704/720/740)Mount using the self tapping screws(nominal size: 3.0 x 4 pcs.) for installation.For models with flow adjustment valvePipingWhen connecting piping to the product, a spanner should be used on the metal piping attachment only.Using a spanner on other parts may damage the product.In particular, do not let the spanner come into contact with the M8 connector.The connector can be easily damaged.If the tightening torque is exceeded, the product can be broken. If the correct tightening torque is not applied, the fittings may become loose.Avoid any sealing tape getting inside the piping.Ensure there is no leakage from loose piping.3/824 mm 1/227 mm 3/432 mm Tighten to the specified torque for piping.The tightening torque for connection threads is shown in the table below.Direct mounting (PF3W711)Mount using the self tapping screws(nominal size: 4.0 x 4 pcs.) for installation.The tightening torque must be 1 to 1.2 Nm.The self tapping screws cannot be re-used.Refer to the outline dimension drawing for mounting hole size.Refer to the product catalogue or SMC website (URL )for more detailed information.WiringWiring of connectorConnections should only be made with the power supply turned off.Use separate routes for the Flow switch wiring and any power or high voltage wiring. Otherwise, malfunction may result due to noise.Ensure that the FG terminal is connected to ground when using a commercially available switch-mode power supply. When a switch-mode power supply isconnected to the product, switching noise will be superimposed and the product specification can no longer be met. This can be prevented by inserting a noise filter, such as a line noise filter and ferrite core, between the switch-mode power supply and the product, or by using a series power supply instead of a 141 mm How to adjust the flow rate(when a flow adjustment valve is mounted)(1) Rotate the knob of the valve to adjust the flowrate to the target value.(2) Be sure to confirm that there is no fluid leakagegenerated after adjustment.the valve several times for re-adjustment, and confirm that there is no fluid leakage.)(3) The flow adjustment valve is not designed forIf the valve is adjusted frequently, fluid may leak due to wear of the internal seal.BodyDisplayBracket mounting (PF3W711)Mount the product (with bracket) usingthe mounting screws supplied (M5 x 4 pcs.).Bracket thickness is approx. 2 mm.2. Press the UP or DOWN button to change the set value.The UP button is to increase and the DOWN button is to decrease the set value.•Press the UP button once to increase by one digit, press and hold to continuously increase.3. Press the SET button to finish the setting.•Press the DOWN button once todecrease by one digit, press and hold tocontinuously decrease.Mounting•Never mount the product in a location where it will be used as a support.•Mount the product so that the fluid flows in the direction indicated by the arrow on the side of the body.•Check the flow characteristics data for pressure loss and the straight inlet pipe length effect on accuracy, to determine inlet piping requirements.•Do not sharply reduce the piping size.•The monitor with integrated display can be rotated. It can be set at 90o intervals clockwise and anticlockwise, and also at 45o and 225o . Rotating the display with excessive force will damage the end stop.Refer to the product catalogue or SMC website (URL )for more detailed information.11/454 mm 11/254 mmBefore UseDigital Flow Switch(Integrated display type)(Integrated display type).Please read this manual carefully before operating the product and make sure you understand its capabilities and limitations. Please keep this manual handy for future reference.Safety InstructionsThese safety instructions are intended to prevent hazardous situations and/or equipment damage.These instructions indicate the level of potential hazard with the labels of"Caution", "Warning" or "Danger". They are all important notes for safety and must be followed in addition to International standards (ISO/IEC) and other safety regulations.OperatorWidth across flats of attachment<Operation>1. Press the SET button in measurement mode to display set values.Set value on the right side of the sub screen flashes.。
澄明度检测仪(设备编号-:)仪器验证性能确认方案
确认方案1 目的本方案目的是验证xxx型澄明度检测仪(设备编号:)的性能。
2 范围本方案适用于xxx型澄明度检测仪(设备编号:)的性能确认。
3 验证对象概述本仪器为天津市天大天发科技有限公司生产的xxx型澄明度检测仪,用于检测可见异物。
4 验证成员职责验证小组的具体成员及职责5 术语N/A6 验证支持性文件6.1 《药品生产验证指南》(2003版)6.2 《澄明度检测仪校准规范》(JJF 1287-2011)6.3 《xxx澄明度检测仪使用说明书》7 验证/确认前准备7.1 人员培训确认:仪器确认开始前应检查确认参与人员均经过培训,并将培训情况记录在人员培训确认表(附件1)中。
7.2 确认前文件资料确认:确认开始前应检查确认所需的文件资料齐全无缺,并将检查情况记录在文件资料确认记录表(附件2)中。
7.3 仪器仪表确认:确认开始前应检查确认所需的仪器仪表是否已经过校准,是否在有效期内,并将检查情况记录在仪器仪表确认表(附件3)中。
8 验证/确认实施8.1 测试项目:照度示值的相对误差8.1.1 目的:确认澄明度检测仪的照度准确性能达到预期要求。
8.1.2 方法:用比较法,校准相对示值误差。
8.1.2.1 将一级(或二级)照度计和澄明度检测仪的照度探头,同时安装在移动工作台夹具上,调整一级(或二级)照度计和澄明度检测仪的照度探头的测试面,使它们到可调遮光板的距离相等。
8.1.2.2 改变可调遮光板和调整澄明度检测仪右边的旋钮,来改变照度。
使一级(或二级)照度计的显示值为某以读数,同时读取被测仪器光照度值,每点测量2次,取平均值。
8.1.3 计算:%ΕΕΕΔΕss100⨯-=式中:△E ——相对示值误差,%;E _——澄明度检测仪的照度计测量平均值,lx ;E s ——一级(或二级)照度计测量值,lx 。
8.1.4 可接受标准:照度示值的相对误差△E±12%。
8.1.5 确认结果:将确认情况填入照度示值的相对误差确认记录表中(附件4)。
DIDP-MSDS
SAFETY DATA SHEETaccording to Regulation (EC) No. 1907/2006Date of issue: 01.09.2013 Version 1.0SECTION 1. Identification of the substance/mixture and of the company/undertaking1.1 Product identifierCatalogue No. 814732Product name Diisodecyl phthalate for synthesisREACH Registration Number A registration number is not available for this substance as thesubstance or its use are exempted from registration according toArticle 2 REACH Regulation (EC) No 1907/2006, the annual tonnagedoes not require a registration or the registration is envisaged for alater registration deadline.1.2 Relevant identified uses of the substance or mixture and uses advised againstIdentified uses Chemical for synthesisFor additional information on uses please refer to the Merck Chemicalsportal ().1.3 Details of the supplier of the safety data sheetCompany Merck KGaA * 64271 Darmstadt * Germany * Phone:+49 6151 72-0 Responsible Department EHS Manager *+61 (3) 8727 6300 * Monday through Friday, 8:00am to5:00pm (EST)Regional representation Merck Pty. LimitedABN 80 001 239 818Ground Floor, Building 1885 Mountain HighwayBayswater VIC 3153 Australia1.4Emergency telephonenumber +61 (3) 8727 6300After hours: CHEMCALL +64 4 917 9888 Poisons Information Centre: 13 1126SECTION 2. Hazards identification2.1 Classification of the substance or mixtureClassification (REGULATION (EC) No 1272/2008)Chronic aquatic toxicity, Category 4, H413For the full text of the H-Statements mentioned in this Section, see Section 16.Classification (67/548/EEC or 1999/45/EC)Dangerous for the environment R53For the full text of the R-phrases mentioned in this Section, see Section 16.2.2 Label elementsLabelling (REGULATION (EC) No 1272/2008)Hazard statementsH413 May cause long lasting harmful effects to aquatic life.Product name Diisodecyl phthalate for synthesisPrecautionary statementsPreventionP273 Avoid release to the environment.Reduced labelling (≤125 ml)Hazard statementsH413 May cause long lasting harmful effects to aquatic life.CAS-No. 26761-40-02.3 Other hazardsNone known.SECTION 3. Composition/information on ingredients3.1 SubstanceFormula C₂₈H₄₆O₄ (Hill)CAS-No. 26761-40-0EC-No. 247-977-1Molar mass 446,66 g/molHazardous components (REGULATION (EC) No 1272/2008)Chemical Name(Concentration)CAS-No. Registration number Classificationdiisodecyl phthalate(<= 100% )26761-40-0 *) Chronic aquatic toxicity, Category 4, H413*) A registration number is not available for this substance as the substance or its use are exempted from registration according to Article2 REACH Regulation (EC) No 1907/2006, the annual tonnage does not require a registration or the registration is envisaged for a laterregistration deadline.For the full text of the H-Statements mentioned in this Section, see Section 16.Hazardous components(1999/45/EC)Chemical Name(Concentration)CAS-No. Classificationdiisodecyl phthalate (<= 100% )26761-40-0 R53For the full text of the R-phrases mentioned in this Section, see Section 16.3.2 Preparationnot applicableSECTION 4. First aid measures4.1 Description of first aid measuresAfter inhalation: fresh air.After skin contact: wash off with plenty of water. Remove contaminated clothing.After eye contact: rinse out with plenty of water.After swallowing: make victim drink water (two glasses at most). Consult doctor if feeling unwell.4.2 Most important symptoms and effects, both acute and delayedProduct name Diisodecyl phthalate for synthesisWe have no description of any toxic symptoms.4.3 Indication of any immediate medical attention and special treatment neededNo information available.SECTION 5. Firefighting measures5.1 Extinguishing mediaSuitable extinguishing mediaCarbon dioxide (CO2), Dry powder, FoamUnsuitable extinguishing mediaFor this substance/mixture no limitations of extinguishing agents are given.5.2 Special hazards arising from the substance or mixtureCombustible materialForms explosive mixtures with air on intense heating.Development of hazardous combustion gases or vapours possible in the event of fire.5.3 Advice for firefightersSpecial protective equipment for firefightersIn the event of fire, wear self-contained breathing apparatus.Further informationPrevent fire extinguishing water from contaminating surface water or the ground water system.SECTION 6. Accidental release measures6.1 Personal precautions, protective equipment and emergency proceduresAdvice for non-emergency personnel: Do not breathe vapours, aerosols. Ensure adequate ventilation. Evacuate the danger area, observe emergency procedures, consult an expert.Advice for emergency responders: Protective equipment see section 8.6.2 Environmental precautionsDo not empty into drains.6.3 Methods and materials for containment and cleaning upCover drains. Collect, bind, and pump off spills.Observe possible material restrictions (see sections 7 and 10).Take up with liquid-absorbent material (e.g. Chemizorb® ). Dispose of properly. Clean upaffected area.6.4 Reference to other sectionsIndications about waste treatment see section 13.SECTION 7. Handling and storage7.1 Precautions for safe handlingAdvice on safe handlingObserve label precautions.Hygiene measuresChange contaminated clothing. Wash hands after working with substance.7.2 Conditions for safe storage, including any incompatibilitiesStorage conditionsTightly closed.Product name Diisodecyl phthalate for synthesisStore at +15°C to +25°C.7.3 Specific end use(s)Apart from the uses mentioned in section 1.2 no other specific uses are stipulated.SECTION 8. Exposure controls/personal protection8.1 Control parametersContains no substances with occupational exposure limit values.8.2 Exposure controlsEngineering measuresTechnical measures and appropriate working operations should be given priority over the use of personal protective equipment.See section 7.1.Individual protection measuresProtective clothing needs to be selected specifically for the workplace, depending onconcentrations and quantities of the hazardous substances handled. The chemical resistance of the protective equipment should be enquired at the respective supplier.Eye/face protectionSafety glassesHand protectionnot requiredRespiratory protectionrequired when vapours/aerosols are generated.Recommended Filter type: Filter A (acc. to DIN 3181) for vapours of organic compoundsThe entrepeneur has to ensure that maintenance, cleaning and testing of respiratory protective devices are carried out according to the instructions of the producer. These measures have to be properly documented.Environmental exposure controlsDo not empty into drains.SECTION 9. Physical and chemical properties9.1 Information on basic physical and chemical propertiesForm liquidColour colourlessOdour odourlessOdour Threshold No information available.pH at 20 °CneutralMelting point-50 °CProduct name Diisodecyl phthalate for synthesis Boiling point/boiling range250 - 267 °Cat 7 hPaMethod: DIN 53171 Flash point 240 °CMethod: c.c.Evaporation rate No information available.Flammability (solid, gas) not applicableLower explosion limit 0,3 %(V)Upper explosion limit No information available.Vapour pressure 0,1 hPaat 20 °CRelative vapour density 15,5Relative density 0,97 g/cm³at 20 °CWater solubility 0,00028 g/lat 24 °CPartition coefficient: n-octanol/water log Pow: 10,28 (calculated)Potential bioaccumulation (Lit.)Auto-ignition temperature No information available.Decomposition temperature No information available.Viscosity, dynamic 105 - 140 mPa.sat 20 °CExplosive properties Not classified as explosive.Oxidizing properties none9.2 Other dataIgnition temperature 380 °CMethod: DIN 51794SECTION 10. Stability and reactivity10.1 ReactivityForms explosive mixtures with air on intense heating.10.2 Chemical stabilityThe product is chemically stable under standard ambient conditions (room temperature) .10.3 Possibility of hazardous reactionsViolent reactions possible with:Product name Diisodecyl phthalate for synthesisBases, Strong oxidizing agents10.4 Conditions to avoidStrong heating.A range from approx. 15 Kelvin below the flash point is to be rated as critical.10.5 Incompatible materialsvarious plastics10.6 Hazardous decomposition productsno information availableSECTION 11. Toxicological information11.1 Information on toxicological effectsAcute oral toxicityLD50 rat: > 5.000 mg/kg (External MSDS)Acute inhalation toxicityThis information is not available.Acute dermal toxicityLD50 rabbit: > 3.160 mg/kg (RTECS)Skin irritationThis information is not available.Eye irritationThis information is not available.SensitisationThis information is not available.Germ cell mutagenicityThis information is not available.CarcinogenicityThis information is not available.Reproductive toxicityThis information is not available.TeratogenicityThis information is not available.Specific target organ toxicity - single exposureThis information is not available.Specific target organ toxicity - repeated exposureThis information is not available.Aspiration hazardThis information is not available.11.2 Further informationHazardous properties cannot be excluded but are unlikely when the product is handled appropriately.Further data:Handle in accordance with good industrial hygiene and safety practice.SECTION 12. Ecological information12.1 ToxicityProduct name Diisodecyl phthalate for synthesisToxicity to daphnia and other aquatic invertebratesEC50 Daphnia magna (Water flea): 500 mg/l; 48 h (above the solubility limit in the test medium) (External MSDS)Toxicity to algaeIC50 Desmodesmus subspicatus (green algae): 500 mg/l; 72 h (above the solubility limit in the test medium) (External MSDS)12.2 Persistence and degradabilityBiodegradability42 %; 21 d(HSDB)Not readily biodegradable.12.3 Bioaccumulative potentialPartition coefficient: n-octanol/waterlog Pow: 10,28(calculated)Potential bioaccumulation (Lit.)12.4 Mobility in soilNo information available.12.5 Results of PBT and vPvB assessmentPBT/vPvB assessment not available as chemical safety assessment not required/not conducted.12.6 Other adverse effectsAdditional ecological informationWhen discharged properly, no impairments in the function of adapted biological wastewater treatment plants are to be expected.Further information on ecologyDischarge into the environment must be avoided.SECTION 13. Disposal considerationsWaste treatment methodsWaste material must be disposed of in accordance with the Directive on waste 2008/98/EC as well as other national and local regulations. Leave chemicals in original containers. No mixing with other waste. Handle uncleaned containers like the product itself.See for processes regarding the return of chemicals and containers, or contact us there if you have further questions.SECTION 14. Transport informationLand transport (ADR/RID)14.1 - 14.6Not classified as dangerous in the meaning of transportregulations.Inland waterway transport (ADN)Not relevantAir transport (IATA)14.1 - 14.6Not classified as dangerous in the meaning of transportregulations.Sea transport (IMDG)Product name Diisodecyl phthalate for synthesis14.1 - 14.6Not classified as dangerous in the meaning of transportregulations.14.7 Transport in bulk according to Annex II of MARPOL 73/78 and the IBC CodeNot relevantSECTION 15. Regulatory information15.1 Safety, health and environmental regulations/legislation specific for the substance or mixtureNational legislationStorage class 10 - 1315.2 Chemical Safety AssessmentFor this product a chemical safety assessment was not carried out.SECTION 16. Other informationFull text of H-Statements referred to under sections 2 and 3.H413 May cause long lasting harmful effects to aquatic life.Full text of R-phrases referred to under sections 2 and 3R53 May cause long-term adverse effects in the aquatic environment.Training adviceProvide adequate information, instruction and training for operators.Labelling (67/548/EEC or 1999/45/EC)R-phrase(s) 53 May cause long-term adverse effects in the aquaticenvironment.S-phrase(s) 61 Avoid release to the environment. Refer to specialinstructions/ Safety data sheets.EC-No.247-977-1Reduced labelling (≤125 ml)R-phrase(s) 53May cause long-term adverse effects in the aquatic environment.Key or legend to abbreviations and acronyms used in the safety data sheetUsed abbreviations and acronyms can be looked up at .The information contained herein is based on the present state of our knowledge. It characterises the product with regard to the appropriate safety precautions. It does not represent a guarantee of any properties of the product.。
Lab manual 1303说明书
Apr 17, 1995 LAB MANUAL 1303.0 1303 LIQUID LIMIT DETERMINATIONAASHTO Designation T 891303.1DEFINITIONThe Liquid Limit of a soil is that water content, as determined in accordancewith the following procedure, at which the soil passes from a plastic to aliquid state.1303.2APPARATUSA. Evaporating Dish - A porcelain dish (preferably unglazed) about115mm (4 1/2 inches) in diameter.B. Spatula - A spatula having a blade about 75mm (3 inches) in lengthand about 20mm (3/4 inches) in width.C. Liquid Limit Device - A mechanical device consisting of a brass dishand carriage as described and shown in AASHTO T 89.D. Grooving Tool - A combined grooving tool and gauge conforming tothe dimensions as shown in AASHTO T 89.E. Containers - Suitable containers with lids which will prevent loss ofmoisture prior to and during weighing. Containers should befabricated from corrosion-resistant material. One container isneeded for each moisture content determination.F. Balance - A balance conforming to the requirements of AASHTO M231, Class C, with a readability, sensitivity of 0.01 grams and anaccuracy of 0.02 grams.G. Oven - A thermostatically-controlled, drying oven capable ofmaintaining a temperature of 110 ± 5 °C (230 ± 9 °F) for dryingmoisture samples.1303.3Adjustment of the Mechanical DeviceA. Inspection1. Check the liquid limit device to determine that it is in goodworking order.2. The pin connecting the cup shall not be worn sufficiently topermit side play.Apr 17, 1995 LAB MANUAL 1303.3A3. The screws connecting the cup to the hanger arm shall betight.4. A cup that has been grooved from use shall be replaced.5. The grooving tool shall be inspected to determine that criticaldimensions conform to AASHTO T 89.B. Adjustments1. By means of the gauge on the handle of the grooving tool, andthe adjustment plate on the liquid limit device, the height towhich the cup is lifted shall be adjusted so that the point onthe cup which comes in contact with the base is exactly 10mm± 2µm above the base.2. Determine the point on the cup which comes in contact withthe base.a. For new cups, place a piece of carbon paper on thebase. Allowing the cup to drop several times will markthe contact spot.b. For used cups, a slightly worn spot will be present.3. After the contact point is determined place a piece of maskingtape across the bottom of the cup. The edge of the tape, awayfrom the hanger, should bisect the contact spot on the cup andremain parallel with the axis of the cup hanger. See Section1303.10 for a diagram of the cup and a figure showing thelocation of the tape.4. Turn the crank until the cup is raised to its maximum height.Slide the gauge under the cup from the front. Observewhether the gauge contacts the cup or the tape. If the tapeedge and the cup are both contacted the height isapproximately correct. If not, adjust the cup untilsimultaneous contact is made.5. The adjustment plate shall then be secured by tightening thescrews. With the gauge still in place the adjustment shall bechecked by revolving the crank several times. If theadjustment is correct a slight ringing or clicking sound will beheard when the cam strikes the cam follower. If the cup israised off the gauge or no sound is heard further adjustmentsshall be made.Apr 17, 1995 LAB MANUAL 1303.3B6. Always remove the tape after completion of the adjustments. 1303.4PROCEDURE - STANDARD METHOD (AASHTO T 89, Method A)(Refer to Section 1301)A. A soil sample of about 100 grams of material passing the 425µm(#40) sieve shall be placed in the evaporating dish and thoroughlymixed with distilled or demineralized water by alternately andrepeatedly, stirring, kneading and chopping with a spatula. Furtheradditions of water shall be made in small (1-3ml) increments. Witheach increment, the water shall be thoroughly mixed with the soilbefore another increment of water is added. Take approximately a10 gram sample from the mixed soil and lay aside to season for usein the plastic limit test. (See Section 1304.)NOTE 1: Once testing has begun NO additional dry soil shall be added to the moistened soil. If too much water hasbeen added, the sample shall be discarded, or the sample shall be mixed and kneaded until natural evaporationlowers the closure point into an acceptable range.NOTE 2: Some soils absorb water more slowly than others so that it is possible to add the water so fast that a falseliquid limit value is obtained. This can be avoided if the sample is mixed thoroughly or more time is allowed.B. When sufficient water has been mixed with the soil to form a uniformmass of stiff consistency, a sufficient quantity of this mixture is placedin the liquid cup and spread out by use of the spatula. The soil shallbe leveled with the spatula and trimmed to a depth of 100µm at thepoint of its maximum thickness.C. The soil in the cup shall be divided by a firm stroke of the groovingtool along the diameter through the centerline of the cam follower sothat a clean sharp groove of the proper dimensions will be formed.To avoid tearing of the sides of the groove or slipping of the soil cakeon the cup, 6 strokes maximum from front to back or back to frontshall be permitted. The depth of the groove should be increased witheach stroke and only the last stroke should scrape the bottom of thecup.D. The cup containing the sample shall be lifted and dropped by turningthe crank at the rate of two revolutions per second until the two sidesof the sample come in contact at the bottom of the groove along adistance of about 12mm (1/2 inch). Do not hold the base of themachine while turning the crank. Record the number of blowsrequired to close the groove. (A motorized device is acceptableprovided it produces the same liquid limit values.)NOTE 3: Frequently check the liquid limit device's adjustment and tighten thescrews connecting the brass cup to the hanger arm.March 1, 2023 LAB MANUAL 1303.4EE. A slice of soil approximately the width of the spatula extending fromedge to edge of the soil cake at right angles to the groove, includingthat portion of the groove in which the soil flowed together, shall beremoved and placed in a suitable container.F. The container and soil shall be weighed and the weight recorded.The soil in the container shall be oven-dried to a constant weight at110 ± 5 °C (230 ± 9 °F) and weighed. This weight shall be recordedand the loss in weight due to drying shall be recorded as the weightof water. (1303 Figure 1)G. Transfer the remaining soil in the cup to the evaporating dish. Washand dry the cup and grooving tool in preparation for the next trial.H. The foregoing operations shall be repeated for at least two additionalportions of the sample to which sufficient water has been added tobring the soil to a more fluid condition. The object of this procedureis to obtain samples of such consistency that at least onedetermination will be made in each of the following ranges: 25-35blows, 20-30 blows and 15-25 blows so the range in the threedeterminations is at least 10 blows. (EXAMPLE: 28-23-18 blows.)Ideally, a spread greater than 10 blows is desired in thedeterminations.March 1 , 2023 LAB MANUAL 1303.61303.6CALCULATIONS for STANDARD METHOD (Three points)A. The water content of the soil shall be expressed as the moisturecontent in percentage of the weight of the oven-dried soil andcalculated as follows:Weight of Water% Moisture =X 100Weight of Oven-dried SoilAs in the example (Can #1):3.02% Moisture =X 100 = 28.90.44NOTE 5: See Form #2485 (Section 1303.8)B. A "flow curve" representing the relation between moisture contentand corresponding number of blows shall be plotted on a semilogarithmic graph. The flow curve shall be a straight line drawn asnearly as possible through the three or more plotted points. SeeForm #2485 (Section 1303.8)C. Liquid Limit - The moisture content corresponding to the intersectionof the flow curve at 25 blows shall be taken as the liquid limit of thesoil. Report this value to the nearest whole number.Apr 17, 1995 LAB MANUAL 1303.8 1303.8 EXAMPLE - FORM # 2485Apr 17, 1995 LAB MANUAL 1303.9 1303.9EXAMPLE - CHART TABLES for ALTERNATE METHODApr 17, 1995 LAB MANUAL 1303.10 1303.10LIQUID LIMIT DEVICE。
硫酸软骨素钠质量安全标准及关键控制点研究进展
赵琳,姜雨,兰韬,等. 硫酸软骨素钠质量安全标准及关键控制点研究进展[J]. 食品工业科技,2022,43(19):7−13. doi:10.13386/j.issn1002-0306.2022030218ZHAO Lin, JIANG Yu, LAN Tao, et al. Review on Quality Safety Standards and Critical Control Points of Chondroitin Sulfate Sodium[J]. Science and Technology of Food Industry, 2022, 43(19): 7−13. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022030218· 青年编委专栏—食品及相关产品质量安全及法规标准(客座主编:兰韬、田明) ·硫酸软骨素钠质量安全标准及关键控制点研究进展赵 琳1,姜 雨2,兰 韬1,吴 琦1,张梦妍1,尹秀文2,刘洪宇2, *,云振宇1,*(1.中国标准化研究院农业食品标准化研究所,北京 100191;2.国家市场监督管理总局食品审评中心,北京 100160)摘 要:硫酸软骨素钠是从动物软骨组织中提取的天然酸性黏多糖,主要作为一种抗骨关节炎药品和保健食品在世界范围内被广泛应用。
由于硫酸软骨素钠的结构、物理化学特征、生理活性会因动物种类、组织、提取工艺的不同而存在差异,使得硫酸软骨素钠的质量安全控制存在难度。
国内外针对硫酸软骨素钠都制定有相应标准,本文以中国、美国、日本、欧洲药典收载的硫酸软骨素钠原料标准为依据,进行分析、归纳和总结,综述了硫酸软骨素钠质量安全标准化发展现状和趋势。
结合最新的研究成果,进一步提炼影响硫酸软骨素钠质量安全的关键控制点,对来源、潜在外源污染物、掺假等因素进行深入分析与探讨,有助于监管部门、生产企业准确把握影响硫酸软骨素钠质量安全的风险源。
亚砷酸根溶液标准物质cas号
标题:亚砷酸根溶液标准物质CAS号及其重要性一、亚砷酸根溶液标准物质的定义亚砷酸根溶液标准物质是用于分析化学、环境监测和质量控制的一种重要化学试剂。
它是由国家相关部门认可的,具有一定生产工艺和检测方法的标准物质。
二、亚砷酸根溶液标准物质CAS号的意义CAS号是化学物质的唯一标识符号,由美国化学学会根据化学物质的结构和组成编制而成。
CAS号的正确使用有助于统一化学物质的命名和识别,有效提高化学品信息的传递和共享效率。
亚砷酸根溶液标准物质的CAS号的正确使用能够确保其在生产、使用和运输过程中的准确识别,有利于质量控制和事故应急处理。
三、如何正确获取亚砷酸根溶液标准物质CAS号要正确获取亚砷酸根溶液标准物质的CAS号,首先需要确认其生产厂家或供应商。
随后可以通过国家相关部门的冠方全球信息站或相关化学品数据库进行查询,或者直接向生产厂家或供应商交流获取。
四、亚砷酸根溶液标准物质CAS号的重要性1. 有利于化学品的准确识别亚砷酸根溶液标准物质CAS号的使用有助于确保其在生产、使用和运输过程中的准确识别,避免因识别错误导致的事故和健康风险。
2. 有助于质量控制正确使用亚砷酸根溶液标准物质CAS号能够帮助质量控制部门更好地监测和管理化学试剂的生产质量,确保产品符合标准要求。
3. 有助于事故应急处理在事故发生时,准确的CAS号能够帮助有关部门更快地获取到化学品的相关信息,有针对性地进行事故应急处理,最大程度地减少事故对人体和环境的损害。
五、结语亚砷酸根溶液标准物质CAS号的正确使用对于化学品的生产、使用和管理具有重要意义。
希望广大从事化学品生产、使用和管理的工作人员能够充分认识到CAS号的重要性,合理正确地使用化学品的CAS 号,确保化学品的安全生产和使用。
六、亚砷酸根溶液标准物质CAS号的普及和推广尽管亚砷酸根溶液标准物质CAS号的重要性不言而喻,但在实际生产和使用过程中,仍然存在一定的普及和推广难度。
有必要加强相关部门和企业对亚砷酸根溶液标准物质CAS号的普及和推广工作。
ASTM D 413
clamps,mandrels,calibrated masses,and mass carriers.Thesupporting frame is of such design that clamps for stripspecimens hang on it vertically and that mandrels for ringspecimens are supported on it horizontally.The frame hassufficient height to permit the mass carrier to be suspendedfrom the test specimens by means of clamps and to hang freelyduring the progress of the test.Provision also is made tosupport the mandrels so that they revolve freely with minimumfriction.Suitable apparatus is shown in Fig.1and Fig.2.6.Test Specimens6.1Strip Specimens—Type A —Plane strips having a widthof 25+3,−0mm (1+0.125,−0in.),and a minimum lengthsuch as to permit 180°peel separation over sufficient distanceto indicate the adhesion value.6.1.1Cut the specimen to 25+3,−0mm (1+0.125−0in.)wide.The thickness will vary according to the constructionof the article being tested.The maximum thickness of thespecimen is limited to 13mm (0.5in.).To comply with thisrequirement,slice or buff the specimen.The ply or layer beingseparated should never be over 6.5mm (0.25in.)thick.6.1.2Cut the specimen from the article in such a mannerthat the adhered parts have the same width where practicable.The technique used in 6.2.2and 6.2.3may be applied here.When necessary,or specified,cut only the layer to be separated (by application of load)to the prescribed width.In such cases,remove the portions of that layer remaining outside of the test width to avoid edge constriction during separation.6.1.3Curved specimens for test in strip form shall have curvature only in the length dimension of the specimen.6.2Strip Specimens—Type B —The same as Type A,with the exception of 90°peel and the separation line in the center of the specimen.6.2.1Cut the specimen 35mm (13⁄8in.)wide.Remove the excess plies to obtain a thickness of 6mm (1⁄4in.)and leave the separation line in the center of the specimen to ensure a 90°peel.6.2.2Buff to a width of 30mm (11⁄8in.)with a coarse grit emery cloth (grit No.40)with care to prevent burning or gumming the sides of the specimen.6.2.3Make a 2-mm (1⁄16-in.)deep slit with a knife along each side exactly where the specimen is to be separated during e a knife with an adjustable blade where only the desired depth of cut (2mm)of blade is exposed.6.3Ring Specimens —Closed rings having a width of 25mm (1in.)and maximum internal diameter of 100mm (4in.).6.3.1Mount the article on a smooth,close-fitting,slightly tapered wooden mandrel.6.3.2Rotate the mandrel (a lathe is preferred)and cut 25-mm (1-in.)wide ring sections by forcing a sharp pointed knife gradually through the article.6.3.3Cut rings with internal diameters over 100mm (4in.)through and open to form strip specimens.7.Procedure 7.1Strip Specimen:Type A,180°Peel —Measure the width of the strip cut to the nearest 0.2mm (0.01in.)and record.Separate the parts to be tested by hand at one end of the strip specimen and at a sufficient distance to permit the jaws of the testing clamp to be attached.Suspend the strip from the supporting frame by the separated end,holding in the jaws of the testing clamp all separated ends except the one under test.Attach to the lower end of the test specimen a minimum mass sufficient to maintain the strip specimen in approximately a vertical position.Or,hold the specimen against a vertical plate in such a manner as to keep the specimen in approximately a vertical position during the test to ensure a 180°peel.Apply a specified or known mass by means of a clamp and mass carrier to the layer of which the adhesion is being determined.Include the mass of the clamp and carrier in the total mass causing separation.Release the mass slowly without jerking and in such a manner that the separating layer is stripped from the specimen at an angle of approximately 180°.7.2Strip Specimen:Type B,90°Peel —Test specimens in the same manner as Type A,with the exception that the unpeeled portion of the specimen is kept in a horizontal position using a plate,if necessary,to ensure a 90°peel.7.3Ring Specimens —Place the ring specimen snugly on a mandrel that has an outside diameter substantially the same as the internal diameter of the ring.Separate the parts to be tested sufficiently by hand to permit the jaws of the testing clamp to be attached.With the mandrel resting on the supportingframe,Dimen-sion mm in.Dimen-sion mm in.A 75.03N 10.01⁄8B 45.011⁄4P 90.031⁄2C 37.511⁄2R 30.011⁄4D 15.03⁄8S 20.03⁄4E 40.0111⁄16T 18.023⁄32F 15.01⁄8U 30.011⁄8G 10.011⁄18V 3.01⁄8H 11.013⁄32W 6.01⁄4J 13.01⁄2X 3.01⁄8K 8.01⁄16Y 3.07⁄64L 16.03⁄8Z 8.05⁄16M 50.011⁄8AA 6.07⁄32AB 75.03FIG.1Clamp for AdhesionTestapply a known or specified mass by means of the clamp and amass carrier to the layer of which the adhesion is being tested.Include the mass of the clamp and carrier in the total masscausing separation.Release the mass slowly without jerkingand in such a manner that the separating layer is stripped fromthe specimen at an angle of approximately 90°.7.4Rate of Separation —Record the time needed to com-plete the separation using a stop watch or a watch having asecond hand.Remove the mass and measure the lengthstripped between marks placed at the beginning and end of thetest on the portion other than that stripped.MACHINE METHOD8.Apparatus8.1A tension testing machine,power-driven,accurate towithin 61%is used for measuring the force required toseparate the layers of the test specimen.A constant rate ofextension testing machine satisfies this condition and is pre-ferred although an inclination-balance,pendulum-type,or aspring-balance apparatus may be used.Requirements of thetesting machine are in 8.2.1to 8.2.58.2.6.8.2Testing Machine :8.2.1The testing machine shall be capable of being operatedwithout any device for maintaining maximum load indication.For pendulum-type machines,do not engage pawls that preventthe mass lever from swinging freely.8.2.2The machine shall be equipped with the chart wherethe distance separated is one axis and the applied force is theother axis of coordinates.The preferred chart speed is the sameas the cross-head speed for ring specimens and one half thecross-head speed for strip specimens.8.2.3The force applied shall be greater than 15%and less than 85%of the capacity of the machine.8.2.4Grips —Strip specimens shall be held in the testing machine by grips that clamp firmly and prevent slipping at all times during the test.For ring specimens,replace the grip attached to the recording head of the machine with a freely rotating mandrel with an outside diameter substantially the same as the inside diameter of the ring specimen.Mount the mandrel so that its axis of rotation is in the plane of the ply being separated and the applied force is normal to the tangent of the ring circumference at the line of separation.8.2.5The preferred rate of travel of the power-actuated grip is 0.8mm/s (2in./min)for strip specimen Type A,2.5mm/s (6in./min)for Type B,and 0.4mm/s (1in./min)for ring specimens.These rates are to be uniform throughout the tests.9.Test Specimens 9.1Prepare the specimens in accordance with Section 6.10.Procedure 10.1Strip Specimens:Type A,180°Peel —Measure the width of the cut strip to the nearest 0.2mm (0.01in.)and record.Separate the parts to be tested by hand at one end of the test specimen and at a sufficient distance to permit grips of the machine to be attached.Attach the separated end of the specimen,with all separate parts except the one under test securely gripped,to the recording head by means of a clamp,using care to adjust it symmetrically in order that the tension shall be distributed uniformly.Provide for maintaining the strip during the test approximately in the plane of the clamps.This may be done either by attaching the minimum mass required to the free end of the specimen or by holding the specimenagainstFIG.2Mandrels and Frame for Static Mass AdhesionTesta plate attached to the stationary clamp but,in either case,take into account the added mass in determining the force causing separation.Grip that layer of the specimen of which the adhesion is to be tested symmetrically andfirmly without twisting in the power-actuated clamp.Adjust the autographic mechanism and chart to zero and start the machine.Strip the separating layer from the specimen at an angle of approxi-mately180°,and continue the separation for a sufficient distance to indicate the adhesion value.10.2Strip Specimen:Type B,90°Peel—Separate by hand a sufficient distance along the separation line in the center of the strip to permit the grips of the machine to be attached.Make provision to keep the unpeeled portion of the test specimen in a horizontal position using a plate if necessary to ensure a90°peel.Peel along the previously cut separation layer for40to 100mm(11⁄2to4in.).10.3Ring Specimens—Separate by hand a sufficient length of a layer of the specimen to be tested to permit the power-actuated clamp of the machine to be attached.Place the specimen snugly on the test mandrel.With the mandrel attached to the recording head of the machine and the separated layer gripped symmetrically andfirmly without twisting in the power-actuated clamp,adjust the autographic mechanism and chart to zero and start the machine.Strip the separating layer from the specimen at an angle of approximately90°to the tangent of the specimen surface,and continue the separation for a sufficient distance to indicate the adhesion value.During the test,the mandrel shall rotate freely so as to maintain the line of separation at all times approximately in the same position.PRECAUTIONS,INTERPRETATION,CALCULATION,AND REPORT11.Precautions11.1Tearing:11.1.1If,during a test,the substrate rubber begins to tear instead of separating at the bonded interface,cut the material being torn with a knife up to the surface of contact between the two parts and start the test again.11.1.2If one of the substrate rubbers repeatedly tears, instead of separating from the other part at the bonded interface,a satisfactory result may be secured in the static-mass method by reducing the amount of the mass used if this is permitted.In case of repeated tearing when using the machine test method,take as the result of the test the average load at which tearing of the substrate rubber occurs.11.2Effect of Temperature—The results of this test are affected by temperature.Elevating the temperature causes a faster rate of stripping under a given load.The temperature during test shall therefore be2362°C(73.163.6°F)and the actual temperature shall be recorded.12.Interpretation of Results12.1In the static-mass test method,no stripping is started unless a certain mass is used.Small increments in mass do not progressively cause proportional increases in rate of separa-tion.With increasing mass the rate increases slowly atfirst and finally very rapidly.Rate of separation must therefore be interpreted carefully.A specimen required to separate not more than0.4mm/s(1in./min)under a force of90N(20lbf)might be regarded as very inferior if the test result was2mm/s(5 in./min).The same specimen might not strip at all under a force of67N(15lbf)and might meet the requirement with a force of80N(18lbf).12.2The true adhesion value is not determined in case the specimens repeatedly tear.The test,however,indicates that the strength of adhesion exceeds the strength of the material and that the adhesion value is not less than the result obtained.In cases of tearing,the results should be so designated.12.3Adhesion values may differ between different plies of the same article of plied construction and also at different points along the same ply.The adhesion value of one ply to another is taken as the average result of the test over a reasonable distance of separation.When possible,a distance of separation of at least100mm(4in.)shall be used.13.Calculation13.1For the Static-Mass Test Method,report the adhesion value as separation rate per unit width under a stated force,as follows:mm/s for252mm width under N forcein./s for12in.width under lbf(1) If a width other than25mm(1in.)was used,correct the separation by multiplying the rate by the ratio of actual width to the desired width.Include both the rate and the actual width in the report.13.2For the machine test method,the autographic chart constitutes the report,but the value of the adhesion is deter-mined by drawing on the chart the best average line between the maximum and minimum force values.The force so indicated,expressed in newtons per metre(or pounds-force per inch)is divided by the width measured in10.1for separation at the rate used and is reported as the adhesion strength,as follows:Adhesion Strength5N/m~lbf/in.!5force/actual width(2) Show both the force and actual width in the report.14.Report14.1The report shall include the following:14.1.1Results of the adhesion test expressed in accordance with Sections12and13,14.1.2All observations and recorded data on which the results are based,14.1.3Date of manufacture or vulcanization of rubber,if known,14.1.4Date of test,14.1.5Statement of the method used,(Strip Type A,Strip Type B,or Ring;Static-Mass or Machine),14.1.6Temperature of test room,and14.1.7Dimensions of the test specimen.15.Precision and Bias15.1Precision and bias do not exist for this method because resources necessary for round-robin testing have not beenforthcoming.16.Keywords16.1adhesion;fabric;rubberThe American Society for Testing and Materials takes no position respecting the validity of any patent rights asserted in connection with any item mentioned in this ers of this standard are expressly advised that determination of the validity of any suchpatent rights,and the risk of infringement of such rights,are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed everyfive years and if not revised,either reapproved or withdrawn.Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM Headquarters.Your comments will receive careful consideration at a meeting of the responsibletechnical committee,which you may attend.If you feel that your comments have not received a fair hearing you should make yourviews known to the ASTM Committee on Standards,100Barr Harbor Drive,West Conshohocken,PA19428.。
Phosphatidylcholine Assay Kit 产品说明书
Phosphatidylcholine Assay Kit Catalog Number MAK049Storage Temperature –20 °CTECHNICAL BULLETINProduct DescriptionPhosphatidylcholine (PC) accounts for more than 50% of the phospholipids composing mammalian plasma membranes and is particularly enriched in theextracellular leaflet. PC is synthesized in the liver and is required for lipoprotein assembly and secretion. PC is cleaved by phospholipase D, which hydrolyses the choline head, producing the signaling intermediate phosphatidic acid.In this assay, PC concentration is determined by acoupled enzyme reaction, which results in a colorimetric (570 nm)/fluorometric (λex = 535/λem = 587 nm) product, proportional to the PC present.ComponentsThe kit is sufficient for 100 assays in 96 well plates.PC Assay Buffer25 mL Catalog Number MAK049AFluorescent Peroxidase Substrate, in DMSO0.2 mL Catalog Number MAK049B PC Hydrolysis Enzyme1 vl Catalog Number MAK049C PC Development Mix1 vl Catalog Number MAK049D PC Standard, 10 µmole1 vlCatalog Number MAK049EReagents and Equipment Required but Not Provided.• 96 well flat-bottom plate –It is recommended to useblack plates with clear bottoms for fluorescence assays and clear plates for colorimetric assays.• Fluorescence or spectrophotometric multiwell platereaderPrecautions and DisclaimerThis product is for R&D use only, not for drug,household, or other uses. Please consult the Material Safety Data Sheet for information regarding hazards and safe handling practices.Preparation InstructionsBriefly centrifuge vials before opening. Use ultrapure water for the preparation of reagents. To maintain reagent integrity, avoid repeated freeze/thaw cycles.PC Assay Buffer –Allow buffer to come to roomtemperature before use.Fluorescent Peroxidase Substrate –Thaw at roomtemperature to melt the solution prior to use.Aliquot and store protected from light and moisture at –20 °C. Upon thawing, the Fluorescent Peroxidase Substrate is ready-to-use in the colorimetric assay.For the fluorescence assay, dilute an aliquot of the Fluorescent Peroxidase Substrate 5 to 10-fold with PC Assay Buffer, just prior to use. This will reduce the background of the fluorescence assay.PC Hydrolysis Enzyme and PC Development Mix –Reconstitute each with 220 µL of PC Assay Buffer. Mix well by pipetting, then aliquot and store,protected from light, at –20 °C. Use within 2 months of reconstitution and keep cold while in use.PC Standard –Reconstitute in 200 µL of water to0generate a 50 mM (50 nmole/µL) PC Standard solution. Mix well by pipetting until it forms a uniform suspension, then aliquot and store at –20 °C. Use within 2 months of reconstitution and keep cold while in use.Storage/StabilityThe kit is shipped on wet ice. Storage at –20 °C, protected from light, is recommended.2ProcedureAll samples and standards should be run in duplicate. PC Standards for Colorimetric DetectionDilute 10 µL of the 50 mM (50 nmole/µL) PC Standard Solution with 990 µL of water to prepare a 0.5 mM (0.5 nmole/µL) standard solution. Add 0, 2, 4, 6, 8,10 µL of the 0.5 mM PC standard solution into a 96 well plate, generating 0 (blank), 1, 2, 3, 4, and 5 nmole/well standards. Add PC Assay Buffer to each well to bring the volume to 50 µL.PC Standards for Fluorometric DetectionDilute 10 µL of the 50 mM (50 nmole/µL) PC Standard Solution with 990 µL of water to prepare a 0.5 mM (0.5 nmole/µL) standard solution.Dilute 10 µL of the 0.5 mM standard solution with 90 µL of water to generate a 0.05 mM (0.05 nmole/µL). Add 0, 2, 4, 6, 8, 10 µL of the 0.05 mM PC standard solution into a96 well plate, generating 0 (blank), 0.1, 0.2, 0.3, 0.4, and 0.5 nmole/well standards. Add PC Assay Buffer to each well to bring the volume to 50 µL.Sample PreparationTissue (10 mg) or cells (2 ×106) should be rapidly homogenized in 4 volumes of cold PC Assay buffer. Centrifuge at 13,000 ×g for 10 minutes at 4 °C to remove insoluble material.Serum samples may be assayed directly.Bring samples to a final volume of50 µL with PC Assay Buffer.For unknown samples, it is suggested to test several sample dilutions to ensure the readings are within the linear range of the standard curve.Choline present in the sample can generate background. To control for choline background, include a blank sample for each sample by omitting the PC Hydrolysis Enzyme in the Reaction Mix. Assay Reaction1.Set up the Master Reaction Mixes according to thescheme in Table 1. 50 µL of the appropriate Master Reaction Mix is required for each reaction (well). Table 1.Reaction Mixes2.Add 50 µL of the appropriate Reaction Mix to eachof the wells. Mix well using a horizontal shaker orby pipetting, and incubate the reaction for30 minutes at room temperature. Protect the platefrom light during the incubation.3.For colorimetric assays, measure the absorbanceat 570 nm (A570). For fluorometric assays, measure fluorescence intensity (λex= 535/λem= 587 nm).3 ResultsCalculationsThe background for the assays is the value obtained for the 0 (blank) PC Standard. Correct for the background by subtracting the 0 (blank) value from all readings. Background values can be significant and must be subtracted from all readings. Use the values obtained from the appropriate PC standards to plot a standard curve.Note: A new standard curve must be set up each time the assay is run.Subtract the blank sample value from the sample reading to obtain the corrected measurement. Using the corrected measurement, the amount of PC present in the sample may be determined from the standard curve Concentration of PCS a/S v= CS a= Amount of PC in unknown sample (nmole) from standard curveS v= Sample volume (µL) added into the wellsC = Concentration of PC in samplePC molecular weight: 768 g/moleSample CalculationAmount of PC (S a) = 5.84 nmole(from standard curve)Sample volume (S v) = 50 µLConcentration of PC in sample5.84 nmole/50 µL = 0.1168 nmole/µL0.1168 nmole/µL ×768 ng/nmole= 89.7 ng/µL4LS,MAM 09/12-1©2012 Sigma-Aldrich Co. LLC. All rights reserved. SIGMA-ALDRICH is a trademark of Sigma-Aldrich Co. LLC, registered in the US and other countries. Sigma brand products are sold through Sigma-Aldrich, Inc. Purchaser must determine the suitability of the product(s) for their particular use. Additional terms and conditions may apply. Please see product information on the Sigma-Aldrich website at and/or on the reverse side of the invoice or packing slip.。
AR20系列电阻调节器及相关配件说明书
WiringDiscrete wiring methodNames of individual partsSUP port4114Describing stationsTerminal board box is installed on the right sideTerminal board box is installed on the left side Red Green 1Above set position Appropriate set position Green 2Below set position1. Insert the lead wire connector into the connector key groove.2. Tighten the connector by hand using the knurl, rotating clockwise.3. Install the other end of the wires using the correct colours.1. Mount the conduit in the terminal board box. Refer to the manufacturers catalogue for the conduit mounting method.2. Insert the cable through the conduit and install the wires according to the terminal board layout below.3. Tighten the conduit. Do not hold down the terminal board box or switch while tightening the conduit. The tightening torque should be 5 Nm maximum.Concentrated wiring methodSettingSet the detection distance using the LED level meter and setting handle.While setting, pull out the setting handle illustrated right.Do not release the setting handle, as it will return to its normal position and the handle will no longer turn.Before pulling outSetting handle pulled outNOTE•If the detection nozzle is exposed to splashes of water or cutting oil, do not allow backflow from the detection nozzle to the switch body. Install the switch body at a position higher than the detection nozzle wherever possible.•The air outlet is provided on the setting dial section of the air catch sensor. Do not turn off air supply to the switch if water or cutting oil splashes around the setting dial.•The switch enclosure conforms to IP66 and the solenoid valve conforms to IP65. The pressure gauge and the regulator have open constructions. Take greater protection measures in an environment where water splashes, oil or spatters from welding may occur.Air Catch SensorOperation ManualISA2Thank you for purchasing an SMC ISA2 Series Air Catch Sensor.Please read this manual carefully before operating the product and make sure you understand its capabilities and limitations.Please keep this manual handy for future reference.To obtain more detailed information about operating this product, please refer to the SMC website (URL ) or contact SMC directly.These safety instructions are intended to prevent hazardous situations and/or equipment damage.These instructions indicate the level of potential hazard with the labels of"Caution", "Warning" or "Danger". They are all important notes for safety and must be followed in addition to International standards (ISO/IEC) and other safety regulations.OperatorSafety InstructionsMounting and InstallationOUT 1OUT 2OUT 3OUT 4OUT 5OUT 6DC (-)NCDC (+)12DC(+)NC 3DC(-)Brown -Blue 4OUTBlackMaintenanceRefer to the product catalogue or SMC website(URL ) for more information about wiring.1. Set the expansion packing (ISA-7-B) in the concave of the SUP port for expansion switches.2. Mount the convex of the expansion switch onto the existing switch.3. Mount the two brackets (ISA-3-A) in their positions.∗: Fasten the screws temporarily.4. Make sure that an expansion packing is set in the concave of theexisting switch SUP port.5. Fit the convex of the existing switch onto the concave of the added switch.6. Mount the existing bracket.∗: Fasten the screws temporarily.2. Assembly1. Tighten the fasteners to a torque of 1.2 Nm.2. Install the air pipes and confirm that there is no air leakage.3. Tightening1. Disassembly1. Loosen the screws to remove two brackets, one each from the front and back surfaces.2. Split the switch slowly so as not to disengage the O-ring of the SUP port.MountingManifold expansion Note: Specifications are subject to change without prior notice and any obligation on the part of the manufacturer.© 2011-2015 SMC Corporation All Rights Reserved Akihabara UDX 15F, 4-14-1, Sotokanda, Chiyoda-ku, Tokyo 101-0021, JAPAN Phone: +81 3-5207-8249 Fax: +81 3-5298-5362URL How to reset the product after a power cut or forcible de-energizing The setting of the product will be retained as it was before a power cut or de-energizing.The output condition is also basically recovered to that before a power cut or de-energizing, but may change depending on the operating environment.Therefore, check the safety of the whole installation before operating the product. If the installation is using accurate control, wait until the product has warmed up (approximately 10 minutes).SpecificationsOutline with Dimensions (in mm)Refer to the product catalogue or SMC website (URL ) for more information about the product specifications and outline dimensions.PS ※※-OMN0005-E。
LAQUAtwin-Na-11盐氮檢測仪操作手冊说明书
CODE: GZ0000460286Instruction Manual (Operation)COMPACT WATER QUALITY METER LAQUAtwin-Na-11SpecificationsItems in packageConsumable parts sold separately Part NamesNotePress the switches 0.5 seconds or more unless otherwise specified.Initial SetupAttaching/detaching the sensorNoteBe careful not to twist the waterproof gasket.Inserting/removing batteriesElectrode conditioningNote●Before using the sensor for the first time or after several days of disuse, perform electrode conditioning.●Perform calibration after electrode condition-ing.1.Place some drops of 2000 ppm standard solution to the flat sensor.2.Wait a few hours before use.There is no need to switch the meter ON.3.Clean the flat sensor with running water.ModelLAQUAtwin-Na-11Target Sodium ion (Na +)Measurement principle ISE method Minimum sample volume More than 0.3 mL *1Measure-ment range2 to 9900 [unit: ppm or mg/L]Resolution (default)Display range:Resolution 2 to 99:1100 to 990:101000 to 9900:100[unit: ppm or mg/L]Calibration Up to 2 pointsDefault: 150 ppm and 2000 ppm Accuracy *2±10% of reading valueWaterproofIP67 (no failure when immersed in water at a depth of 1 m for 30 min) *3Display Custom (monochrome) digital LCDwith backlightOperating environment Temperature: 5︒C to 40︒CHumidity: 85% relative humidity orless (no condensation)Power CR2032 batteries (⨯2)Battery life Approx. 400 h continuous operation(backlight off mode)*4Material ABS epoxy (main material)Dimensions 164 ⨯ 29 ⨯ 20 mm (excluding projec-tions)Mass Approx. 50 g (excluding batteries)*10.05 mL or more if sampling sheet B (sold sepa-rately) is used.*2The closeness of agreement between a mea-sured value and an actual value of standard solu-tion after two-point calibration using 150 ppm and 2000 ppm standard solutions.●The standard solution used for the later cali-bration was measured after two-point calibra-tion at 150 ppm and 2000 ppm.●The calibration and measurement are per-formed at the same temperature.●The error of standard solutions and rounding error (±1 digit) are not included.*3The meter cannot be used underwater.*4When the backlight is used, battery life willshorten.ItemsQuantitySensor S0221Meter1Storage case 1BatteriesCR20322Standard solution150 ppm 12000 ppm1Pipette1Sampling sheet B (5 sheet-pack)1Instruction manual (Operation)1Instruction manual (Before use)1Items Specifications Part No.SensorS022, Na +3200459867Standard solution Y022L, Na + 150 ppm3200457724Y022H, Na + 2000 ppm 3200457723Sampling sheet BY046, 100 sheet-pack 32000538581Flat sensor2Light shield cover 3Liquid junction 4Response mem-brane 5Lithium batteries 6MEAS switch 7ON/OFF switch 8CAL switch9Waterproof gasket 10Strap eyeletAttaching the sensor 1.Power OFF the meter.2.Confirm that the waterproofing gasket is clean and undamaged.3.shown.Detaching the sensor 1.Power OFF the meter.2.Lift the sensor tongue tip and slide the sensor a little away from the meter.3.Pull out the sensor all the way from the meter. Inserting the batteries 1.Power OFF the meter.2.Slide both batteries into the battery case as shown.Be sure to use two CR2032 batteries, and put them with the plus sides(+) upwards.Removing the batteries 1.Power OFF the meter.e a ball-point pen or other tool to pry the batter-ies out from the clips as shown.Basic OperationCalibrationCalibration is required before measurement.Use standard solution within the measurement range in the specifications. See also the tip of “How to select standard solution” below.Tip●Calibration values are saved even if the meteris switched OFF.●Calibration value is rewritten if calibration isrepeated using the same standard solution.TipHow to select standard solution:The following table show an example of the rela-tionship between the concentrations of targeted samples and standard solution used for calibra-tion.For accurate measurement, calibrate using 2points of standard solution with a tenfold or moreconcentration difference encompassing the tar-get concentration.When the concentration to be measured is veryhigh or very low, accuracy may be poorer.MeasurementPower ON1.Press and hold the ON/OFF switch.The power is switched ON,and the meter modelnumber is displayed on theLCD.Power OFF1.Press and hold the ON/OFF switch.The power is switched OFF.Calibration pointsThe number of calibration points is up to 2.Multi-point calibration1.Set the concentrations of standard solutionfor calibration referring to " 1st calibra-tion point setting" (page 5) and " 2nd cal-ibration point setting" (page 5).The 1st point is set to 150 ppm and the 2ndpoint is set to 2000 ppm by the default.2.Open the light shield cover and place somedrops of the standard solution on the flatsensor taking care to cover the entire flatsensor.Rinsing the sensor with the standard solutionbeforehand will provide a more accuratecalibration as it will reduce sample crossovercontamination.3.Close the light shield cover and press theCAL switch.The meter enters the CAL mode and blinks thedisplay of the set 1st-point concentration.Pressing the MEAS switch switches thedisplayed value between the setconcentrations.4.With the set concentration of the 1st pointdisplayed.After the calibration is complete,stop blinking and the measured value isdisplayed.The calibration value at 25 C is displayed for 1s and the display returns to the measurementmode automatically.5.Open the light shield cover and remove thestandard solution. Then remove moistureon the sensor by gently dabbing with a softtissue.This completes the 1st point calibration.6.To perform 2nd point calibration, repeatsteps 2. to 5.Calibration errorIf blinks and Er4 (error dis-play) appears, the calibrationhas failed.Perform electrode conditioning.Check that the correct standard solution is used,and repeat calibration after cleaning the sensor.If the calibration repeatedly fails when using thecorrect standard solution(s), the sensor mayhave deteriorated. Replace the sensor with newone.[unit: ppm]Targeted sampleconcentrationStandard solutionLow High200020009000150150200015 15*150*How to prepare 15 ppm standard solution:Mix one part 150 ppm standard solution to 9 partspurified water (1:9 volume ratio).Sample setting1.Open the light shield cover and put somedrops of sample on the flat sensor to coverthe entire flat sensor.2.Close the light shield cover.Measurement modeThe auto stable (AS) mode and the auto hold(AH) mode can be selected. Refer to " Mea-surement mode change" (page 5) for the opera-tion to set the measurement mode.Auto stable (AS) mode1.Confirm that the meter is in the measure-ment mode, and place a sample on the sen-sor.locked.2.appears.Auto hold (AH) modeand will not change until the MEAS switch ispressed for the next measurement.1.Confirm that the meter is in the measure-ment mode, and place a sample on the sen-sor.2.Press the MEAS switch.The auto hold function isactivated.blinks until themeasured value hasstabilized.When the measured value is stable, stopsblinking and the displayed value is locked with3.Document the displayed value.4.Press the MEAS switch.disappears.Be sure to perform this step before starting thenext measurement. Or, you may mistake thedisplayed hold value for the next measuredvalue.●If a measured value is out of the specifiedmeasurement range, "Or" is displayed for upper range and "Ur" is displayed for under range.●When you have a problem with the calibrationor measurement, refer to frequently asked questions.Sampling sheetFor a minute sample●Note that reaction between sample and sam-pling sheet B may affect the measured value.●Handle sampling sheet B with tweezers tominimize possible contamination.●Be sure to close the light shield cover duringmeasurement to minimize possible sample evaporation.For a sample containing tiny particles If tiny particles are contained in a sample, such as an extract from soil, the particles influence measurement results. Use the sampling sheet holder cover and sampling sheet B sold sepa-rately to counteract the influence.The sampling sheet holder cover does not shield the sensor from light, which affects the sensor. When using the sampling sheet holder cover, shield the flat sensor from light with an alterna-tive.1.Replace the light shield cover with the sam-pling sheet holder cover.2.Put a piece of sampling sheet B on the flatsensor and close the sampling sheet holder cover.3.Put 4 or 5 drops of sample on the samplingsheet B.The display mode switches among concentration(the unit depends the setting), temperature, andvoltage by pressing the MEAS switch in the ASmode.MaintenanceAppendixInterfering ionsSelectivity coefficient is a concentration ratio ofthe interfering ion against the target ion, whichaffects the target ion measurement value. Forexample, selectivity coefficient of interfering ionagainst target ion is 1 ⨯ 10-2, which means for thesame concentration of interfering ion and targetion coexisting in a sample, the target measure-ment shows approximately 1 ⨯ 10-2 (1%) higherresult.minute sample.covered with only 50to 100 μL sample.Storage1.Clean the sensor with tap water.2.Dab gently with soft tissue or cloth toremove moisture on the sensor and meter.NoteEspecially be sure to treat the flat sensor gentlyto prevent damaging it.3.Close the light shield cover and the slidecap before storing the meter.Temperature sensor adjustmentTo perform accurate measurement with correc-tion for temperature effects, follow the stepsbelow. Normally this is not necessary.1.Ready a reference thermometer, and allowthe meter and reference thermometer toreach to room temperature.2.Set the display mode to temperature refer-ring to " Measurement display change"(page 3).3.Press the CAL switch.The meter displays the setting screen fortarget temperature.4.Press the MEAS switch to adjust the dis-played temperature on the meter to matchthe temperature indicated by the referencethermometer.Pressing the MEAS switch increases thedisplayed temperature. After the displayedtemperature reaches 40°C, it returns to 5°C.5.Press the CAL switch again to apply thedisplayed value to the adjustment.The adjustment starts. The adjusted valueblinks with and displayed.After the adjustment is complete, the adjustedvalue stops blinking with MEAS anddisplayed.If Er4 (error display) appears, the adjustmenthas failed. Retry the above steps increasingthe time spent on the step 1.If the adjustment repeatedly fails, the sensormay have deteriorated. Replace the sensorwith new one.Initializing calibration dataInitialize calibration in the following cases.●To delete the calibration data●If the number of points for the last calibration isuncertain.●After the sensor is replaced.1.Press and hold the CAL and ON/OFFswitches for over 3 seconds when themeter is switched OFF to Initialize calibra-tion.After a moment of all segment indication, thesoftware version is displayed.And then, the displaychanges as shown right.2.Press the CAL switch.All calibration data is reset.When the initialization ofcalibration data is complete,End appears.The meter automatically switches OFF.Initializing the settingsAll setup choices are erased. The meter is resetto the factory default values.1.Press and hold the MEAS, CAL and ON/OFFswitches for over 3 seconds when themeter is switched OFF to enter the initial-ization.After a moment of all segment indication, thesoftware version is displayed.And then, the displaychanges as shown right.2.Press the CAL switch.All calibration data is reset.When the initialization ofsettings is complete, Endappears.The meter automatically switches OFF.Target Sodium ion (Na+)Interfering ions andselectivity coefficientsK+, Rb+: 1 ⨯ 10-2(at 10-3 mol/L Na+)pH range 3 pH to 9 pH(at 10-3 mol/L Na+)Frequently asked questionsEr4 is dis-played during the calibra-tion Please note that if you press the CAL switch in mV or temperature display mode, Er4 is displayed. This is because there is no calibration facility available for these modes.Er1 is dis-played soon power ON.The internal IC in the meter may be defective. Perform meter initializa-tion.If Er1 is still displayed after the initial-ization, the internal IC in the meter is defective. Replace the meter with a new one (the meter cannot be repaired).Er2 is dis-played right after power ON.The internal IC in the meter is defec-tive. Replace the meter with a new one (the meter cannot be repaired).Er3 is dis-played right after power ON.The internal IC in the meter is defec-tive. Replace the meter with a new one (the meter cannot be repaired).What factors interfere measure-ment?Acids influence measurement results. Measure within the range from 3 pH to 9 pH. Also, high-level monovalent cations, such as K+, may cause measurement errors. Refer to " Interfering ions" (page 3) for details.Are there any helpful tips or precautions to be aware for measure-ment?When the sample amount is enough, washing the sensor twice or so with the sample allows more accurate measurement.Residue between the light shield cover and flat sensor prevents accu-rate measurement. Before measure-ment of the next sample, wash the sensor with tap water and remove moisture.Question AnswerCan I pre-pare stan-dard solutions myself?You can prepare standard solutions by dissolving sodium chloride in ion-exchanged water to the specified concentration.Question AnswerSetup ModeThe setup mode allows the user to customize the meter to his specific needs.To enter the setup mode, press and hold the MEAS and ON/OFF switches for over 3 seconds when the meter is switched OFF. All the LCD segments appear and then the meter enters the setup mode.Tip●To have the changes apply, you need to go through the entire steps from “Setup mode entry” to “Setup completion” shown below. To leave a setting as it is, just press CAL switch in the setting.●To exit the setup mode with no change of settings, press the ON/OFF switch earlier than pressing CAL switch in the last step but one, or the “Backlight setting” step.Setup mode entryUnit settingThe display units can be changed.1st calibration point settingThe concentration of the 1st calibration point can be set.NoteIf you changed either of the calibration concentration settings, calibrate again at the both set concentrations before mea-surement. When either calibration concen-tration is changed, the calibration data are initialized.2nd calibration point settingThe concentration of the 2nd calibration point can be set.*In calibration point setting, pressing the MEAS switch increases the displayed value. After the displayed value reaches 9800, it returns to 3.Measurement mode changeThe measurement mode can be switched.* Measurement display change is available in the AS mode. Refer to " Measurement display change" (page 3).Multiplying compensation settingThe coefficient (0.01 to 9.90) to be applied to the measured value can be set. The compensated result is displayed as the measured value. The default setting is 1.00.Backlight settingThe backlight can be switched to ON or OFF.Setup completion31, Miyanonishi-cho, Kisshoin Minami-ku, Kyoto,。
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DECATHLON STANDARD
Document issued by TESTING LABORATORY – Decathlon Campus 4, Bd de Mons - BP 299 59665 Villeneuve d'Ascq Cedex - FRANCE
DS - 413 Version A
Others associated or required documents ISO 3696: Water for analytical laboratory use – Specification and test methods SCOPE This Decathlon Standard can be applied to textiles in any form. OBJECTIVES Determine the pH of the aqueous extract of textiles. PRINCIPLE The pH value of an aqueous extract of a textile is measured electrometrically at room temperature (20-25° C) by means of a glass electrode. The result is expressed to the nearest 0,1 pH-unit and if the difference between the pH values is more than 0,2, repeat the method. REQUIREMENTS ON EQUIPMENT & CONSUMABLES Reagents - Distilled or deionized water of at least grade 3 as defined in ISO 3696, with a pH between 5,0 and 7,0. - Potassium chloride solution (KCl), concentration of 0,1 mol.l-1, prepared by using distilled or deionized water above (find in following suppliers: VWR International, Merck…). - Buffer solutions for the calibration of the pH-meter before measurement, with a pH around 4, 7 and 9 (cf. ISO 3071: 2005 Annexe A). Equipment - Clean glassware used for that kind of test ONLY and washed every time with distilled or deionized water in between experiments: stoppered glass or propylene flasks for the preparation of the aqueous extract, 150 ml-beakers. - pH-meter, with a glass electrode, accurate to at least 0,1 pH-units. - Balance, accurate to 0,01g. - Mechanical shaker, to-and-fro movement at a rate of 60 min-1 or a rotational frequency of 30 min-1. ENVIRONMENTAL CONDITIONS The test has to be carried out at a temperature of 20-25 ° C.
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Codification
DECATHLON STANDARD
SAMPLE PREPARATION
DS-413 Version A
Before manipulating the sample, hands should be washed properly and dried. To avoid contamination, handle the material as little as possible. Take three laboratory samples of 2,00 ± 0,05 g each representative of a bulk of the textile material. Cut the samples into pieces of 5 mm sides or of such a size as to allow the test samples to wet out quickly. TEST PROTOCOL REQUIREMENTS Extraction Prepare the extract in triplicate as follows: Place 2,00 ± 0,05 g of cut samples and 100 ml of potassium chloride solution into a stoppered flask. Shake the flask for a short period by hand to ensure that the textile material is properly wet out, and then shake it mechanically for 2h ± 5 min. Record the temperature of the KCl solution used. Calibration of the pH-meter Calibrate the pH-meter at the temperature of the extract measurement by using at least two buffer solutions. Rinse the electrode with distilled or deionized water and dry it properly after the use of each buffer solution. Then immerse the electrode in the potassium chloride solution for conditioning. Measurement of the pH First, take a clean beaker and measure the pH of the potassium chloride solution. Record the pH value. Then do not rinse the electrode. Take the first flask, decant the extract and immerse immediately the electrode to a depth of at least 10 mm and stir gently until the pH value stabilizes. Do not record this pH value.
OBJECT AND SCOPE This Decathlon Standard specifies a method based on the International Standard ISO 3071: 2005 to determine the pH of the aqueous extract of all types of textile.
DECATHLON STANDARD
DS-413 Version A
COPYRIGHT WARNING All mentioned external reference standards shall be owned by the user of this document.
PURPOSE This document is an internal Test Standard. It contains the general test requirements which are applicable in all the internal or external laboratories where the tests are carried out. When stated, this document defines the useful criteria to establish the conformity of a product or a component. This document aims to harmonize choices and possible interpretations of the international test standards. This document does not contain the detailed modalities of implementation of the tests, regarding to specific test equipments and accommodations of the Laboratory. These modalities must appear in Work Instructions written locally by every laboratory.
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Codification
DECATHLON STANDARD