ASTM C471M-2017ae1 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 17a1Standard 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 last rev

2、ision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1NOTECorrected Research Report number in December 2017.1. Scope*1.1 These test methods cover the chemical analysis ofgypsum and gypsum pan

3、el products, including gypsum ready-mixed plaster, gypsum wood-fibered plaster, and gypsumconcrete.1.2 The test methods appear in the following order:SectionsPreparation of Sample 4Complete Procedure 516Alternative Procedure for Analysis of Free Water in 17Gypsum Using a Moisture BalanceAlternative

4、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 MethodDetermination of Sand in Set Plaster 21Wood-Fiber Content

5、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 Panel ProductsGeneral ProvisionsDetermination of Orthorhombic Cycl

6、ooctasulfur (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 Detector (GC/ECD)Determination of Orthorhombic Cyclooctasulfur (S

7、8)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 footnotesthat provide explanatory material. These notes and footnotes(excluding those in tables and figures) shall not be considereda

8、s requirements of the standard.1.4 The values stated in SI units are to be regarded as thestandard.1.5 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety, health,

9、and environmental practices and deter-mine the applicability of regulatory limitations prior to use.1.6 This international standard was developed in accor-dance with internationally recognized principles on standard-ization established in the Decision on Principles for theDevelopment of Internationa

10、l Standards, Guides and Recom-mendations issued by the World Trade Organization TechnicalBarriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:2C11 Terminology Relating to Gypsum and Related BuildingMaterials and SystemsC22/C22M Specification for GypsumC28/C28M Specification fo

11、r Gypsum PlastersC59 Specification for Gypsum Casting Plaster and GypsumMolding PlasterC61 Specification for Gypsum Keenes CementC317/C317M Specification for Gypsum ConcreteC778 Specification for Standard SandC842 Specification for Application of Interior Gypsum Plas-terD1193 Specification for Reage

12、nt WaterD1428 Test Method for Test for Sodium and Potassium InWater and Water-Formed Deposits by Flame Photometry(Withdrawn 1989)3D2013 Practice for Preparing Coal Samples for AnalysisE11 Specification for Woven Wire Test Sieve Cloth and TestSieves1These test methods are under the jurisdiction of AS

13、TM Committee C11 onGypsum and Related Building Materials and Systems and are the direct responsi-bility of Subcommittee C11.01 on Specifications and Test Methods for GypsumProducts.Current edition approved Oct. 1, 2017. Published November 2017. Originallyapproved in 1961. Last previous edition appro

14、ved in 2017 as C471M 17. DOI:10.1520/C0471M-17AE01.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3The last

15、approved version of this historical standard is referenced onwww.astm.org.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United StatesThis international standard was developed in acc

16、ordance with internationally recognized principles on standardization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.1E177 Practice for Use of the T

17、erms Precision and Bias inASTM Test MethodsE691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test Method3. Terminology3.1 DefinitionsDefinitions shall be in accordance withTerminology C11.3.2 Definitions:3.2.1 calibration standard, na chemical mixture contain-ing a

18、 known quantity of the analyte used to relate the measuredanalytical signal to 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 quantifi-cation of S8by monitoring and adjusting for minor variances ininstrument perfor

19、mance.3.2.4 riffle, na hand feed sample divider device thatdivides the sample into parts of approximately the sameweight. (D2013)3.2.5 sample as received, na representative portion of rawgypsum or gypsum product in the state received by the testinglaboratory, including aggregates, impurities and wat

20、er content.3.2.6 surrogate standard, na chemical used to account forextraction efficiency of S8.4. Preparation of Sample4.1 General ProceduresDetails of sample preparation willvary according to the type of material being tested.4.1.1 Sample As ReceivedUse a sufficient amount ofsample such that, afte

21、r sieving, not less than 50 g of samplewill remain for testing. Weigh the entire sample immediatelyafter opening the container in which the material was received.This will become the weight of the sample as received.4.1.2 DryingDry the sample in accordance with Section 7.This will be the weight of t

22、he dried sample.4.1.3 Crushing and GrindingCrush and grind the sampleby hand with a mortar and pestle or by mechanical crushingand grinding equipment to pass a 250-m (No. 60) sieve. Takecare, particularly with mechanical equipment, not to expose thesample to temperatures of more than 52C. Clean the

23、equip-ment thoroughly between samples. Thoroughly remix theground sample and store it in an airtight container to avoidcontamination.4.1.4 RehydratingThoroughly blend and rehydratesamples which contain calcium sulfate in forms other thanCaSO42H2O and natural anhydrite. Place the sample indistilled w

24、ater and keep it wet for not less than 48 h. Dry thehydrated sample in an oven at 45 6 3C to constant weight andrecrush or grind it in accordance with 4.1.3.4.1.5 Sample ReductionThoroughly mix and reduce largesamples as required by quartering or by the use of a riffle toobtain a specimen of approxi

25、mately 50 g.4.2 Gypsum (Specification C22/C22M)Gypsum sampleswill be received in the form of rocks or powder, or both. Ifnecessary crush and reduce the entire dried sample in accor-dance with 4.1.3 and 4.1.5.4.3 Gypsum Plaster, (Specification C28/C28M).4.3.1 Gypsum Ready-Mixed Plaster or Gypsum Wood

26、Fi-bered PlasterScreen the dried sample through a 150-m(No. 100) sieve4and discard the residue retained on the sieve.Reweigh the remaining sample and calculate the percentage ofthe dried sample. Reduce the sample in accordance with 4.1.5.Thoroughly blend and rehydrate the specimen in accordancewith

27、4.1.44.3.2 Gypsum Neat Plaster or Gypsum Gauging PlasterReduce the dried sample in accordance with 4.1.5. Thoroughlyblend and rehydrate the specimen in accordance with 4.1.4.4.4 Gypsum Casting and Molding Plaster, (SpecificationC59)Reduce the dried sample in accordance with 4.1.5.Thoroughly blend an

28、d rehydrate the specimen in accordancewith 4.1.4.4.5 Gypsum Keenes Cement, (Specification C61)Reducethe dried sample in accordance with 4.1.5. Blend in no morethan 1 % molding plaster or K2SO4and rehydrate the specimenin accordance with 4.1.4.4.6 Gypsum Concrete, (Specification C317/C317M)Screen the

29、 dried sample through a 150-m (No. 100) sieve4and discard the residue retained on the sieve. Reweigh theremaining sample and calculate the percentage of the driedsample. Reduce the sample in accordance with 4.1.5. Thor-oughly blend and rehydrate the specimen in accordance with4.1.44.7 Gypsum Panel P

30、roductsCut or break the dried sampleinto small pieces. Using a mortar and pestle, strike the piecesof the sample to loosen the paper face. Remove the pieces ofpaper by hand as they are separated from the core of thegypsum board. Carefully scrape any remaining powder fromthe paper. When all the paper

31、 has been removed from thepieces of the sample, reduce the sample in accordance with4.1.5.COMPLETE PROCEDURE5. Apparatus5.1 Analytical BalanceCapable of weighing the weighingbottles, lids and samples.5.2 BalanceCapable of weighing not less than 100 g at aprecision of 0.001 g.5.3 Drying OvenA mechani

32、cal convection oven set at 456 3C.5.4 DesiccatorCapable of being tightly sealed and con-taining calcium chloride or equivalent desiccant.5.5 Calcining Oven or FurnaceCapable of achieving andmaintaining temperatures to not less than 1000C.5.6 Weighing BottlesBorosilicate glass or ceramic con-tainers

33、with tightly sealable lids.5.7 Hot PlateA controllable hot plate capable of heatingcasseroles to approximately 120C.4Detailed requirements for this sieve are given in Specification E11.C471M 17a125.8 Porcelain CasserolesWith a capacity of 50 to 100 mL.5.9 Filtering Funnels.5.10 Filter Paper.5.11 Por

34、celain Crucibles.5.12 Mortar and Pestle.5.13 Mechanical Jaw CrusherCapable of crushing gyp-sum rocks up to 50 mm diameter.5.14 Mechanical GrinderBurr mill or equivalent capableof grinding the granular output of the jaw crusher specified in5.13.6. Reagents6.1 Purity of ReagentsUse reagent grade chemi

35、cals in alltests. Unless otherwise indicated, use reagents that conform tothe specifications of the Committee on Analytical Reagents ofthe American Chemical Society, where such specifications areavailable.5If it is necessary to use other grades, first ascertainthat the reagent is of sufficiently hig

36、h purity so that its use willnot lessen the accuracy of the determination.6.1.1 Ammonium Chloride (NH4Cl).6.1.2 Ammonium Hydroxide (sp gr 0.90)Concentratedammonium hydroxide (NH4OH).6.1.3 Ammonium Nitrate (25 g/L)Dissolve 25 g of ammo-nium nitrate (NH4NO3) in water and dilute to 1 L.6.1.4 Ammonium O

37、xalate (NH4)2C2O4).6.1.5 Barium Chloride (100 g/L)Dissolve 100 g of bariumchloride (BaCl22H2O) in water and dilute to 1 L.6.1.6 Calcium Chloride (CaCl2)Anhydrous CalciumChloride with a combined water of not more than 5 %.6.1.7 Hydrochloric Acid (sp gr 1.19)Concentrated hydro-chloric acid (HCl).6.1.8

38、 Hydrochloric Acid (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).6.1.11 Potassium Chromate Solution (100 g/L)Dissolve5 g of pota

39、ssium chromate (K2CrO4) in 50 mL of water, mix,add ten drops of 0.05 N silver nitrate (AgNO3) solution, allowto stand for 5 min, and filter.6.1.12 Potassium Permanganate (5.6339 g/L)Dissolve5.6339 g of potassium permanganate (KMnO4) in water anddilute to 1 L.6.1.13 Silver Nitrate, Standard Solution

40、(0.05 N)Prepareand 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 sulfuricacid (H2SO4).6.1.16 Sulfuric Acid (1+6)Carefully mix one volume ofH2SO4(sp gr 1.84) with six volumes of water.6.1.17 Nitric Acid (

41、0.1 N)Mix 1.4 mL of HNO3(sp gr1.42) with 200 mL of water.6.1.18 Phenolphthalein Indicator SolutionDissolve 0.25 gof phenolphthalein in 30 mL of methanol and dilute to 50 mLwith water.6.1.19 Sodium Hydroxide Solution (0.1 N)Dissolve1gofsodium hydroxide (NaOH) in 250 mL of water.6.1.20 WaterReagent wa

42、ter shall be in accordance withSpecification D1193, type II. Specification D1193 gives thefollowing values for type II grade water.Electrical conductivity, max, S/cm at 298 K (25-C) 1.0Electrical resistivity, min, Mcm at 298 K (25-C) 1.0Total organic carbon (TOC), max, g/L 50.0Sodium, max, g/L 5.0Ch

43、lorides max, g/L 5.0Total silica, max, g/L 5.07. Free Water7.1 Significance and UseThe free water analysis deter-mines the amount of free water contained in the sample asopposed to chemically combined water, and prepares thesample for further analysis.7.2 Procedure:7.2.1 Weigh a sample of the materi

44、al as received of not lessthan 50 g to a precision of 0.001 g and spread it out in a thinlayer in a suitable vessel. Place in an oven and dry at 45 6 3Cuntil constant mass has been obtained. The samples are to becooled in a desiccator prior to each weighing. The loss ofweight corresponds to the free

45、 water.7.2.2 Retain the sample in a sealed container or in thedesiccator for further analysis.7.3 Calculation and ReportCalculate and report loss inweight as a percentage of the sample as received or of the driedsample as required.7.4 Precision and Bias:7.4.1 The precision of this test method is bas

46、ed on aninterlaboratory study ofASTM C471M, Standard Test Methodsfor Chemical Analysis of Gypsum and Gypsum Products,conducted in 2016. Each of 17 laboratories analyzed twodifferent gypsum sample types. Every “test result” representsan individual determination, and all participants reported fivetest

47、 results per material. Practice E691 was followed for thedesign and analysis of the data; the details are given in ASTMResearch Report No. C11-1003.67.4.1.1 Repeatability (r)The difference between repetitiveresults obtained by the same operator in a given laboratoryapplying the same test method with

48、 the same apparatus underconstant operating conditions on identical test material withinshort intervals of time would in the long run, in the normal andcorrect operation of the test method, exceed the followingvalues only in one case in 20.(1) Repeatability can be interpreted as maximum differencebe

49、tween two results, obtained under repeatability conditions,5Reagent Chemicals, American Chemical Society Specifications , AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlisted by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.6Supporting data have been filed at ASTM International Headquarter