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5.1  Dialkyldithiocarbamates (DTCs), benzothiazoles, and thiurams are often used as vulcanization accelerators in NRL products. Zinc DTC accelerators are added either directly or are formed in situ during the vulcanization process via reaction between a thiuram(s) and zinc oxide. DTCs, benzothiazoles, and thiurams have been detected in leachates from medical devices made of rubber such as gloves. Studies have shown these chemicals can cause allergic contact dermatitis. A simple selective method to monitor rubber accelerator levels in rubber extracts would be useful for quality control, product screening and research.5.2 This colorimetric assay measures dialkyldithiocarbamates, including zinc dialkyldithiocarbamates (ZDTC), mercaptobenzothiazole (MBT) and thiurams as a total thiol vulcanization accelerator level in rubber products. A UV spectrophotometer with detection at 320 nm is used to measure the ZDTC, mercaptobenzothiazole and thiurams. Sample extracts diluted at 1:20 prior to measurement on the spectrophotometer is usually sufficient to quantify the residual accelerator level from most commercially available rubber gloves; however, sample dilution can be adjusted (from neat extract to > 1:20 dilution) based on analytical needs. Thiurams and ZDTCs complex with cobalt turning the extract to a concentration-dependent shade of green. ZDTCs reacts quickly while thiurams react very slowly (requiring a heat catalyst). Mercaptobenzothiazole does not complex to Co(III), however, it absorbs strongly at 320 nm. It can be distinguished from both ZDTCs and thiurams by its strong absorbance at 320 nm without the cobalt dependent visible green color. Cobalt complexed thiurams and ZDTCs, but not MBT, also have and absorbance at 370 nm (2).1.1 This test method is designed to quantify the amount of total extractable accelerators in natural rubber latex (NRL) and nitrile gloves. Three common classes of rubber accelerators, the mercaptobenzothiazole (MBT), thiuram, and thiocarbamate type compounds can be detected and quantified by this method. If the specific rubber accelerator(s) present in the glove material is not known, quantification is based on zinc dibutyldithiocarbamate (ZDBC) equivalents. This method will not detect all potential rubber accelerators, including mercaptobenzothiazole disulfide, dimorpholine, thioureas and diphenyl diamine.1.2 For the purpose of this test method, the range of chemical accelerator measurement is based on the limit of detection (LOD) established in the performing laboratory.1.3 This test method should be performed by experienced analysts or under the supervision of those experienced in the use of spectroscopy and working with organic solvents.1.4 This test method has not been validated for measurement of long chain dithiocarbamates or accelerators from other rubber products, such as lubricated condoms (1).2 Although this assay has been reported in the literature for the evaluation of accelerator levels in condoms, further validation for accelerator measurement from other rubber products is required by the testing laboratory prior to use.1.5 This test method is not designed to evaluate the potential of rubber materials to induce or elicit Type IV skin sensitization reactions (for Type IV skin sensitization reactions see Test Method D6355). Total extractable accelerator content does not reflect bioavailablity of individual accelerators that are detected and measured by this method. This test method should be used to test and measure the total residual chemical accelerator level in NRL and nitrile gloves under controlled laboratory conditions, and should not be used to describe, appraise, or assess the hazard or risk of these materials or products under actual in-use conditions.1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 This test method, for the determination of protein levels in latex, is primarily intended to test NR, latex, and elastomeric materials for residual protein content. It is assumed that all who use this test method will be trained analysts capable of performing common laboratory procedures skillfully and safely. It is expected that work will be performed in a properly equipped laboratory.1.1 This test method covers an analytical test for determining the amount of total aqueous extractable protein associated with NR, latex, and elastomeric products. Water soluble proteins are extracted in a buffer solution and then precipitated to concentrate them and also to separate them from water soluble substances that may interfere with the determination. The extracted protein is redissolved and quantified colorimetrically by the modified Lowry method using a protein standard.1.2 For the purpose of this test method, the range of protein measurement will be based on the limit of detection and quantitation and recorded in micrograms per dm2 test specimen.1.3 The test method is designed to be accurate and compatible with the industrial environment.1.4 Steps are included in this test method to minimize the effects of interfering substances.1.5 It is recognized that other methods for the analysis of leachable proteins exist and these may be used for routine quality control purposes provided they have been validated and a correlation established against the reference method specified by this test method.1.6 This test method has not been validated for use with lubricated products such as condoms. Condoms with different lubricants as typically marketed, have not been tested in an ASTM ILS to determine if, and if so to what degree, the lubricant interferes with the assay.1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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3.1 This test method provides the means to determine nitrogen containing water extractable materials such as excess and loosely bound tannins, ammonium salts, and nitrates.1.1 This test method covers quantitatively determining the water extractable nitrogen in leather.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The presence of water-soluble extractables in membrane filters can create errors in test procedures employing membrane filters. However, these errors can be eliminated or significantly reduced if the quantity of water-soluble extractables of the specific membrane is previously determined. Certain membrane filter uses require specifications of maximum water-soluble extractable levels. This test method is intended to be a rapid test to determine the loss of water-soluble compounds such as plasticizers or wetting agents from filtration membranes. This test method is not designed to predetermine the performance of a filter, but is significant in determining the percent extractables of membranes from different sources and lot variations from a single source.1.1 This test method covers the gravimetric determination of the water-extractable material present in membrane filters and is applicable over the complete concentration range of extractables.1.2 The analyst should be aware that collaborative data for a bias statement as required by Practice D2777 is not provided. See Section 11 for details.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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Excess soluble sulfate ions in hardened cement can result in reduced durability. This test method is intended to show whether calcium sulfate has been used in cement in such amount to leave excess soluble sulfate in hardened mortar. The test method is used to establish compliance in Specification C 595 for those cements in which optimized SO3 exceeds the table limit. This test method also can provide useful information on other hydraulic cements, such as those specified in Specifications C 150 and C 1157.When this test method is used in conjunction with Test Method C 563, use the appropriate age of test specimens (24 h, 3 days, or 7 days) to coincide with the age of specimens used in Test Method C 563.1.1 This test method covers the measurement of water-extractable SO3 in hardened hydraulic cement mortar. This measurement is assumed to represent unreacted, available sulfate remaining in the mortar.1.1.1 Warning—Fresh hydraulic cementious mixtures are caustic and may cause chemical burns to skin and tissue upon prolonged exposure.1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.3 Values in SI units were obtained by measurement in SI units or by appropriate conversion using the Rules for Conversion and Rounding given in IEEE/ASTM SI-10 Standard of measurements made in other units.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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7.1 This test method is based on subsection 8.3 of Consumer Safety Specification F963, which specifies a test procedure to determine the amount of hazardous metals that have the potential to be present in toys and handled or ingested by children. Since it is possible for users of synthetic turf playing surfaces to handle or ingest particles of synthetic turf infill materials, it is necessary to determine the level of hazardous metals in the synthetic turf infill materials. The limits of hazardous metals used in this specification are based on those specified in Consumer Safety Specification F963, adjusted for statistical error correction factor as described in Consumer Safety Specification F963.AbstractThis specification covers all extractable hazardous metals (man-made or natural) that are intended for use as infill materials for synthetic turf sports surfaces. It specifies the amount of certain metals that have the potential to be extracted from synthetic turf infill materials if ingested. The time, temperature, and pH of the extraction fluid approximate the conditions the infill material would experience in the stomach during the digestive process. The levels of extractable metals are compared to maximum levels allowed in children's toys.This specification includes requirements with respect to performance (hazardous metal content), test methods, sampling, apparatus, reagents, and procedure.1.1 This specification relates to the amount of certain metals that have the potential to be extracted from synthetic turf infill materials if ingested. The time, temperature, and pH of the extraction fluid approximate the conditions the infill material would experience in the stomach during the digestive process. The levels of extractable metals are compared to maximum levels allowed in children’s toys.1.2 This specification applies to all materials (man-made or natural) that are intended for use as infill materials for synthetic turf sports surfaces.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 NRL derived from Hevea contains over 200 proteins a number of which are allergens capable of eliciting Type 1 anaphylactic reactions. Guayule Natural Rubber derived from the Parthenium argentatum plant contains many fewer proteins and at much lower levels than Hevea NRL. While there have been no reports of allergic reactions to GNR proteins at present, they have been shown to induce antibody production in exposed individuals.4 An immunological assay that tests for the presence of GNR has the advantage of providing the specificity and sensitivity that other ASTM standards such as Test Methods D5712 and D6499 do not offer.5.2 This test method describes an immunological method for the quantitation of Guayule natural rubber proteins using rabbit anti-GNR serum. Rabbits immunized with GNR proteins react to the majority of the proteins present, and their sera have the capability to detect most if not all of the proteins in GNR. This test method may be used to determine if a test item contains material derived from a natural source.1.1 This test method covers an immunological method to determine the amount of protein in Guayule Natural Rubber (GNR) and its products using rabbit antisera specific for Guayule Natural Rubber latex proteins. This immunoassay procedure quantitatively measures the level of GNR proteins in solution using an inhibition format. The samples may include but are not restricted to, gloves or other GNR product extracts, and liquid GNR samples which have been collected in order to measure the protein levels.1.2 For the purpose of this test method, the range of protein will be measured in terms of microgram to milligram quantities.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 FDA requirements for maximum extractables are specified for resin and uses. This test method provides a means to determine the amount of hexane-soluble low molecular weight material present in polyolefins. It is applicable to resins containing greater than 0.20 % extractables.1.1 This test method describes an extraction/gravimetric procedure for determination of the amount of hexane soluble low molecular weight material present in polyethylene, polypropylene, ethylene-propylene copolymers, and ethylene-vinyl acetate copolymers. This test method is a modification of the Food and Drug Administration (FDA) procedure for determining hexane extractables of polyolefins. This test method is based upon the presumption that the weight of the residue extract present in the solvent is equal to the amount extracted from the film sample and could therefore be quantified by measuring the weight loss of the extracted film, eliminating the complex and time-consuming evaporation process described in 21 CFR 177.1520.1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.3 The values stated in SI units are to be regarded as the standard. Units used in 21 CFR 177.1520 are also used in this test method. Units are in conformance with Federal Code 21 CFR 177.1520, from which this test method is derived.NOTE 1: There is no known ISO equivalent to this standard.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM D2257-20 Standard Test Method for Extractable Matter in Textiles Active 发布日期 :  1970-01-01 实施日期 : 

5.1 This test method may be used for acceptance testing of commercial shipments.5.1.1 In case of a dispute arising from differences in reported test results using this test method for acceptance testing of commercial shipments, the purchaser and the supplier should conduct comparative tests to determine if there is a statistical bias between the laboratories. Competent statistical assistance is recommended for the investigation of bias. As a minimum, the two parties should take a group of test specimens which are as homogeneous as possible and which are from a lot of material of the type in question. The test specimens should then be randomly assigned in equal numbers to each laboratory for testing. The average results from the two laboratories should be compared using appropriate statistical analysis and a probability level chosen by the two parties before the testing begins. If a bias is found, either its cause must be found and corrected, or the purchaser and supplier must agree to interpret future test results with consideration to the known bias.5.2 This test method is used for the determination of the amounts of naturally present oily or waxy impurities that have not been completely removed from textiles made from animal fibers, and for the determination of the amounts of oily or waxy finishing materials applied to raw materials or textiles during manufacture. See 3.1.1, extractable matter.5.3 The test method may be used as a step in the determination of the commercial weight of fiber, yarn, and textile shipments.5.4 The International Wool Textile Organization specifies the use of a halogenated hydrocarbon, dichloromethane, also called methylene chloride (CH2Cl2) instead of the solvent specified in this test method (IWTO-10-62(E)).5.5 Extractables by mass loss is frequently used for textiles which have a relatively large amount of extractable material to effect a significant mass change.1.1 This test method covers a procedure for determining the extractable material on most fibers, yarns, and fabrics. Three options are included. Option 1 uses heat and Soxhlet extraction apparatus. Option 2 uses room temperature and extraction funnels. Option 3 uses either Option 1 or Option 2 extraction but provides for calculation of extractable matter from the loss in mass of the material due to the extraction rather than the extractable matter residue.NOTE 1: Other standards for the determination of extractable matter in textiles made of specific fibers include: Specification D541, Specification D681, and Test Method D1574.1.1.1 The solvents for use in this method are any solvents that the party or parties concerned agreed on; such as, Halogenated Hydrocarbon (HH) chloroform, tetrachloroethane, alcohol (isopropyl or methyl).1.1.2 This test method may not extract cross-linked finishes or resins which may be on the textile.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. See Sections 6 and 7.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 The quantitative determination of acid-extractable content is useful in evaluating activated carbon samples that contain acid-soluble impurities. These acid-soluble impurities can affect applications of activated carbon.4.2 Limitations of Method—Hydrochloric acid is used in this test method as the extracting acid. All elements or compounds present in the activated carbon sample, which can be acid extracted, are assumed to form water-soluble chloride salts. Hydrochloric acid may not solubilize all impurities of activated carbon.1.1 This test method is to be used for determination of the acid-extractable content of a sample of activated carbon. This test method presupposes the existence of substances other than carbon to be present with activated carbon but does not purport to address or identify those substances which may be present. This test method should be applicable to any form in which activated carbon may exist and requires the performance of Test Method D2866.1.2 This test method requires the use of concentrated hydrochloric acid, which should be used in an appropriate and safe manner, with eye protection, skin protection, and handling carried out in a properly operating fume hood. The proper use of a muffle furnace is addressed in Test Method D2866.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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3.1 This test method is used by black pigment producers and users for product acceptance.1.1 This test method covers the determination of the solvent-extractable material in black pigments such as carbon black, lampblack, and bone black.1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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A knowledge of the quantity of oil and grease present in a waste is helpful in overcoming difficulties in wastewater treatment plant operation, in determining plant efficiencies, and in controlling the subsequent discharge of these materials to receiving streams.When oils and greases are discharged in wastewater or treated effluents, they often cause surface films and shoreline deposits.1.1 These test methods cover the estimation of oil and grease in water and wastewater by a gravimetric determination of fluorocarbon extractable substances from an acidified sample. Also included in this estimation of oil and grease are any other compounds soluble in chlorofluorocarbon-113 and non-volatile under the conditions of test.1.2 The following two test methods are included: SectionsTest Method A-Liquid-Liquid Extraction Test Method B-Soxhlet Extraction 1.3 These test methods are applicable to natural waters and domestic wastewaters. They are also suitable for most industrial wastewaters, although certain wastes may yield low results because of the presence of either excessive concentrations of natural greases or synthetic or modified compounds that are not well recovered by these test methods.1.4 These test methods measure those groups of substance called oil and grease, whether soluble or insoluble, polar or non-polar, or biological or mineral in origin, to the extent these substances partition from the matrix into chlorofluorocarbon-113 and are not volatilized under conditions of the test. (See the Introduction and Section of these test methods.)1.5 Because these test methods include an acidification step prior to extraction, soluble metallic soaps are hydrolyzed and recovered as fatty acids in the extraction step.1.6 These test methods were fully validated by collaborative testing in reagent Type IV water. The information on precision may not apply to other waters. Note 1Refer to companion procedures (Test Method D 3921).1.7 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see 12.1, 13.2, 20.1, and 20.5.

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4.1 Water-extractable chloride, when present in sufficient amount, has a potential to initiate or accelerate corrosion of metals, such as steel, embedded in or contacting a cementitious system, such as mortar, grout, or concrete. This test method is applicable when aggregates contain a high background of naturally occurring chloride (see ACI 222.1–96 ). Test Method C1152/C1152M determines acid-soluble chloride and Test Method C1218/C1218M determines water-soluble chloride. Both Test Methods C1152/C1152M and C1218/C1218M pulverize the sample to a fine powder or fine granular material. The Soxhlet method is intended to use nonpulverized material. Results with some aggregates have shown that the Soxhlet procedure extracts an extremely low amount of chloride, with most of it remaining in the rock, and therefore, it is not available for corrosion.4.2 The Soxhlet extraction apparatus consists of three sections: the boiling flask, which contains reagent water at the beginning of the test; the extractor, which contains the sample inside a thimble; and, the condenser. The extractor functions by boiling the water, which condenses and drips on to the sample. When the water attains a fixed height above the sample, the extractor siphons the water from the thimble back to the boiling flask. The process repeats itself until the test is terminated. (Refer to Fig. 1.)FIG. 1 Soxhlet Extraction Apparatus1.1 This test method provides procedures for sampling and analysis of aggregate for water-extractable chloride using a Soxhlet extractor.NOTE 1: This test method is to be used when significantly high chloride content has been found in aggregates, concretes, or mortars.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The presence of water extractables in ion-exchange resins can cause fouling of other materials downstream and contamination of process water. The quantity of water extractables is sometimes used as a specification to indicate resin quality, and typical values are 0.01 to 0.1 %.5.2 It is recognized that this test method may not remove all potential sloughage products and does not measure volatile compounds. More extensive extraction and identification of compounds may be needed in specific cases.1.1 This test method covers the measurement of water soluble extractable residue from particulate ion-exchange resins based on elevated temperature extraction and gravimetric determination of residue.1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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