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本文(ASTM C471M-2017a Standard Test Methods for Chemical Analysis of Gypsum and Gypsum Products (Metric)《石膏和石膏制品的化学分析标准试验方法(公制)》.pdf)为本站会员(visitstep340)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM C471M-2017a Standard Test Methods for Chemical Analysis of Gypsum and Gypsum Products (Metric)《石膏和石膏制品的化学分析标准试验方法(公制)》.pdf

1、Designation: C471M 171C471M 17aStandard Test Methods forChemical Analysis of Gypsum and Gypsum Products(Metric)1This standard is issued under the fixed designation C471M; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of

2、last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1 NOTECorrected equation reference in 9.6 and restored item (6) to list in 16.1 editorially in August 2017.1. Scope*1.1 These test

3、 methods cover the chemical analysis of gypsum and gypsum panel products, including gypsum ready-mixedplaster, gypsum wood-fibered plaster, and gypsum concrete.1.2 The test methods appear in the following order:SectionsPreparation of Sample 4Complete Procedure 5 16Alternative Procedure for Analysis

4、of Free Water in 17Gypsum Using a Moisture BalanceAlternative Procedure for Analysis of Combined Water in 18Gypsum Using a Moisture BalanceAlternative Procedure for Analysis for Calcium Sulfate by 19Ammonium Acetate MethodAlternative Procedure for Analysis for Sodium Chloride by 20the Coulometric Me

5、thodDetermination of Sand in Set Plaster 21Wood-Fiber Content in Wood-Fiber Gypsum Plaster 22Optional Procedure for Analysis for Sodium by the Atomic 23Absorption MethodOptional Procedure for Analysis for Sodium by Flame 24PhotometryDetermination of Orthorhombic Cyclooctasulfur (S8) in 25Ggypsum Pan

6、el ProductsGeneral ProvisionsDetermination of Orthorhombic Cyclooctasulfur (S8) in 26Gypsum Panel Products by Gas ChromatographEquipped with a Mass Spectrometer (GS/MS)Determination of Orthorhombic Cyclooctasulfur (S8) in 27Gypsum Panel Products by Gas ChromatographEquipped with an Electron Capture

7、Detector (GC/ECD)Determination of Orthorhombic Cyclooctasulfur (S8) in 28Gypsum Panel Products by High-performance LiquidChromatograph Equipped with and Ultraviolet Detector(HPLC UV)1.3 The text of this standard references notes and footnotes that provide explanatory material. These notes and footno

8、tes(excluding those in tables and figures) shall not be considered as requirements of the standard.1.4 The values stated in SI units are to be regarded as the standard.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibilityo

9、f the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability ofregulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardizationestablished

10、in the Decision on Principles for the Development of International Standards, Guides and Recommendations issuedby the World Trade Organization Technical Barriers to Trade (TBT) Committee.1 These test methods are under the jurisdiction of ASTM Committee C11 on Gypsum and Related Building Materials an

11、d Systems and are the direct responsibility ofSubcommittee C11.01 on Specifications and Test Methods for Gypsum Products.Current edition approved June 1, 2017Oct. 1, 2017. Published July 2017November 2017. Originally approved in 1961. Last previous edition approved in 20162017 asC471M 16C471M 17.A.

12、DOI: 10.1520/C0471M-17E01.10.1520/C0471M-17A.This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Becauseit may not be technically possible to adequately depict all changes accurately,

13、 ASTM recommends that users consult prior editions as appropriate. In all cases only the current versionof the standard as published by ASTM is to be considered the official document.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive,

14、 PO Box C700, West Conshohocken, PA 19428-2959. United States12. Referenced Documents2.1 ASTM Standards:2C11 Terminology Relating to Gypsum and Related Building Materials and SystemsC22/C22M Specification for GypsumC28/C28M Specification for Gypsum PlastersC59 Specification for Gypsum Casting Plaste

15、r and Gypsum Molding PlasterC61 Specification for Gypsum Keenes CementC317/C317M Specification for Gypsum ConcreteC778 Specification for Standard SandC842 Specification for Application of Interior Gypsum PlasterD1193 Specification for Reagent WaterD1428 Test Method for Test for Sodium and Potassium

16、In Water and Water-Formed Deposits by Flame Photometry (Withdrawn1989)3D2013 Practice for Preparing Coal Samples for AnalysisE11 Specification for Woven Wire Test Sieve Cloth and Test SievesE177 Practice for Use of the Terms Precision and Bias in ASTM Test MethodsE691 Practice for Conducting an Inte

17、rlaboratory Study to Determine the Precision of a Test Method3. Terminology3.1 DefinitionsDefinitions shall be in accordance with Terminology C11.3.2 Definitions:3.2.1 calibration standard, na chemical mixture containing a known quantity of the analyte used to relate the measuredanalytical signal to

18、 the concentration of the analyte.3.2.2 dried sample, na sample devoid of free water.3.2.3 internal standard, na chemical used in the quantification of S8 by monitoring and adjusting for minor variances ininstrument performance.3.2.4 riffle, na hand feed sample divider device that divides the sample

19、 into parts of approximately the same weight. (D2013)3.2.5 sample as received, na representative portion of raw gypsum or gypsum product in the state received by the testinglaboratory, including aggregates, impurities and water content.3.2.6 surrogate standard, na chemical used to account for extrac

20、tion efficiency of S8.4. Preparation of Sample4.1 General ProceduresDetails of sample preparation will vary according to the type of material being tested.4.1.1 Sample As ReceivedUse a sufficient amount of sample such that, after sieving, not less than 50 g of sample will remainfor testing. Weigh th

21、e entire sample immediately after opening the container in which the material was received. This will becomethe weight of the sample as received.4.1.2 DryingDry the sample in accordance with Section 7. This will be the weight of the dried sample.4.1.3 Crushing and GrindingCrush and grind the sample

22、by hand with a mortar and pestle or by mechanical crushing andgrinding equipment to pass a 250-m (No. 60) sieve. Take care, particularly with mechanical equipment, not to expose the sampleto temperatures of more than 52C. Clean the equipment thoroughly between samples. Thoroughly remix the ground sa

23、mple andstore it in an airtight container to avoid contamination.4.1.4 RehydratingThoroughly blend and rehydrate samples which contain calcium sulfate in forms other than CaSO4 2H2Oand natural anhydrite. Place the sample in distilled water and keep it wet for not less than 48 h. Dry the hydrated sam

24、ple in anoven at 45 6 3C to constant weight and recrush or grind it in accordance with 4.1.3.4.1.5 Sample ReductionThoroughly mix and reduce large samples as required by quartering or by the use of a riffle to obtaina specimen of approximately 50 g.4.2 Gypsum (Specification C22/C22M)Gypsum samples w

25、ill be received in the form of rocks or powder, or both. If necessarycrush and reduce the entire dried sample in accordance with 4.1.3 and 4.1.5.4.3 Gypsum Plaster, (Specification C28/C28M).4.3.1 Gypsum Ready-Mixed Plaster or Gypsum WoodFibered PlasterScreen the dried sample through a 150-m (No. 100

26、)sieve4 and discard the residue retained on the sieve. Reweigh the remaining sample and calculate the percentage of the driedsample. Reduce the sample in accordance with 4.1.5. Thoroughly blend and rehydrate the specimen in accordance with 4.1.42 For referencedASTM standards, visit theASTM website,

27、www.astm.org, or contactASTM Customer Service at serviceastm.org. For Annual Book of ASTM Standardsvolume information, refer to the standards Document Summary page on the ASTM website.3 The last approved version of this historical standard is referenced on www.astm.org.4 Detailed requirements for th

28、is sieve are given in Specification E11.C471M 17a24.3.2 Gypsum Neat Plaster or Gypsum Gauging PlasterReduce the dried sample in accordance with 4.1.5. Thoroughly blendand rehydrate the specimen in accordance with 4.1.4.4.4 Gypsum Casting and Molding Plaster, (Specification C59)Reduce the dried sampl

29、e in accordance with 4.1.5. Thoroughlyblend and rehydrate the specimen in accordance with 4.1.4.4.5 Gypsum Keenes Cement, (Specification C61)Reduce the dried sample in accordance with 4.1.5. Blend in no more than1 % molding plaster or K2SO4 and rehydrate the specimen in accordance with 4.1.4.4.6 Gyp

30、sum Concrete, (Specification C317/C317M)Screen the dried sample through a 150-m (No. 100) sieve4 and discardthe residue retained on the sieve. Reweigh the remaining sample and calculate the percentage of the dried sample. Reduce thesample in accordance with 4.1.5. Thoroughly blend and rehydrate the

31、specimen in accordance with 4.1.44.7 Gypsum Panel ProductsCut or break the dried sample into small pieces. Using a mortar and pestle, strike the pieces ofthe sample to loosen the paper face. Remove the pieces of paper by hand as they are separated from the core of the gypsum board.Carefully scrape a

32、ny remaining powder from the paper. When all the paper has been removed from the pieces of the sample, reducethe sample in accordance with 4.1.5.COMPLETE PROCEDURE5. Apparatus5.1 Analytical BalanceCapable of weighing the weighing bottles, lids and samples.5.2 BalanceCapable of weighing not less than

33、 100 g at a precision of 0.001 g.5.3 Drying OvenA mechanical convection oven set at 45 6 3C.5.4 DesiccatorCapable of being tightly sealed and containing calcium chloride or equivalent desiccant.5.5 Calcining Oven or FurnaceCapable of achieving and maintaining temperatures to not less than 1000C.5.6

34、Weighing BottlesBorosilicate glass or ceramic containers with tightly sealable lids.5.7 Hot PlateA controllable hot plate capable of heating casseroles to approximately 120C.5.8 Porcelain CasserolesWith a capacity of 50 to 100 mL.5.9 Filtering Funnels.5.10 Filter Paper.5.11 Porcelain Crucibles.5.12

35、Mortar and Pestle.5.13 Mechanical Jaw CrusherCapable of crushing gypsum rocks up to 50 mm diameter.5.14 Mechanical GrinderBurr mill or equivalent capable of grinding the granular output of the jaw crusher specified in 5.13.6. Reagents6.1 Purity of ReagentsUse reagent grade chemicals in all tests. Un

36、less otherwise indicated, use reagents that conform to thespecifications of the Committee on Analytical Reagents of the American Chemical Society, where such specifications areavailable.5 If it is necessary to use other grades, first ascertain that the reagent is of sufficiently high purity so that

37、its use will notlessen the accuracy of the determination.6.1.1 Ammonium Chloride (NH4Cl).6.1.2 Ammonium Hydroxide (sp gr 0.90)Concentrated ammonium hydroxide (NH4OH).6.1.3 Ammonium Nitrate (25 g/L)Dissolve 25 g of ammonium nitrate (NH4NO3) in water and dilute to 1 L.6.1.4 Ammonium Oxalate (NH4)2C2O4

38、).6.1.5 Barium Chloride (100 g/L)Dissolve 100 g of barium chloride (BaCl22H2O) in water and dilute to 1 L.6.1.6 Calcium Chloride (CaCl2)Anhydrous Calcium Chloride with a combined water of not more than 5 %.6.1.7 Hydrochloric Acid (sp gr 1.19)Concentrated hydrochloric acid (HCl).6.1.8 Hydrochloric Ac

39、id (1 + 4)Mix one volume of HCl (sp gr 1.19) with four volumes of water.6.1.9 Hydrochloric Acid (1 + 5)Mix one volume of HCl (sp gr 1.19) with five volumes of water.6.1.10 Nitric Acid (sp gr 1.42)Concentrated nitric acid (HNO3).5 Reagent Chemicals, American Chemical Society Specifications , American

40、 Chemical Society, Washington, DC. For suggestions on the testing of reagents not listed bythe American Chemical Society, see Analar Standards for Laboratory Chemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeia and NationalFormulary, U.S. Pharmacopeial Convention, Inc. (USPC)

41、, Rockville, MD.C471M 17a36.1.11 Potassium Chromate Solution (100 g/L)Dissolve 5 g of potassium chromate (K2CrO4) in 50 mL of water, mix, add tendrops of 0.05 N silver nitrate (AgNO3) solution, allow to stand for 5 min, and filter.6.1.12 Potassium Permanganate (5.6339 g/L)Dissolve 5.6339 g of potass

42、ium permanganate (KMnO4) in water and dilute to1 L.6.1.13 Silver Nitrate, Standard Solution (0.05 N)Prepare and standardize a 0.05 N silver nitrate (AgNO3) solution.6.1.14 Sodium Ammonium Phosphate(NaNH4HPO4).6.1.15 Sulfuric Acid (sp gr 1.84)Concentrated sulfuric acid (H2SO4).6.1.16 Sulfuric Acid (1

43、 + 6)Carefully mix one volume of H2SO4 (sp gr 1.84) with six volumes of water.6.1.17 Nitric Acid (0.1 N)Mix 1.4 mL of HNO3 (sp gr 1.42) with 200 mL of water.6.1.18 Phenolphthalein Indicator SolutionDissolve 0.25 g of phenolphthalein in 30 mL of methanol and dilute to 50 mL withwater.6.1.19 Sodium Hy

44、droxide Solution (0.1 N)Dissolve 1 g of sodium hydroxide (NaOH) in 250 mL of water.6.1.20 WaterReagent water shall be in accordance with Specification D1193, type II. Specification D1193 gives the followingvalues for type II grade water.Electrical conductivity, max, S/cm at 298 K (25-C) 1.0Electrica

45、l resistivity, min, Mcm at 298 K (25-C) 1.0Total organic carbon (TOC), max, g/L 50.0Sodium, max, g/L 50.0 5.0Chlorides max, g/L 50.0 5.0Total silica, max, g/L 50.0 5.0Electrical conductivity, max, S/cm at 298 K (25-C) 1.0Electrical resistivity, min, Mcm at 298 K (25-C) 1.0Total organic carbon (TOC),

46、 max, g/L 50.0Sodium, max, g/L 5.0Chlorides max, g/L 5.0Total silica, max, g/L 5.07. Free Water7.1 Significance and UseThe free water analysis determines the amount of free water contained in the sample as opposed tochemically combined water, and prepares the sample for further analysis.7.2 Procedur

47、e:7.2.1 Weigh a sample of the material as received of not less than 50 g to a precision of 0.001 g and spread it out in a thin layerin a suitable vessel. Place in an oven and dry at 45 6 3C for 2 h, then cool until constant mass has been obtained. The samplesare to be cooled in a desiccator and weig

48、h again. prior to each weighing. The loss of weight corresponds to the free water.7.2.2 Retain the sample in a sealed container or in the desiccator for further analysis.7.3 Calculation and ReportCalculate and report loss in weight as a percentage of the sample as received or of the dried sampleas r

49、equired.7.4 Precision and Bias:7.4.1 The precision of this test method is based on an interlaboratory study of ASTM C471M, Standard Test Methods forChemical Analysis of Gypsum and Gypsum Products, conducted in 2016. Each of 17 laboratories analyzed two different gypsumsample types. Every “test result” represents an individual determination, and all participants reported five test results per material.Practice E691 was followed for the design and analysis of the data; the details are given in

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