ASTM D1278-1991a(2007) Standard Test Methods for Rubber from Natural Sources&8212 Chemical Analysis《自然资源中橡胶的标准试验方法 化学分析》.pdf

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1、Designation: D 1278 91a (Reapproved 2007)Standard Test Methods forRubber from Natural SourcesChemical Analysis1This standard is issued under the fixed designation D 1278; 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 (e) indicates an editorial change since the last revision or reapproval.1. Scope1.1 These test methods cover the sampling and chemicalanalysis of solid natural rubber in the forms supplied to therubber

3、 industry.1.2 The analytical procedures appear in the following order:SectionsSampling 5Volatile Matter 6-8Dirt 9-13Ash 14-17Copper (Referee Colorimetric Method) 18-22Copper (Alternative Colorimetric Method) 23-27Copper (Alternative Flame Atomic Absorption Method) 28Manganese (Colorimetric Method) 2

4、9-33Manganese (Alternative Flame Atomic Absorption Method) 34Iron (Colorimetric Method) 35-39Acetone Extract 40-41Rubber Hydrocarbon 42-43Nitrogen 44-451.3 The values stated in SI units are to be regarded as thestandard. The values in parentheses are for information only.1.4 This standard does not p

5、urport 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 and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2

6、D 297 Test Methods for Rubber ProductsChemicalAnalysisD 1193 Specification for Reagent WaterD 1485 Practice for Rubber from Natural SourcesSampling and Sample PreparationD 3533 Test Method for RubberNitrogen Content3D 4004 Test Methods for RubberDetermination of MetalContent by Flame Atomic Absorpti

7、on (AAS) AnalysisD 4483 Practice for Evaluating Precision for Test MethodStandards in the Rubber and Carbon Black ManufacturingIndustriesE11 Specification for Wire Cloth and Sieves for TestingPurposesE 131 Terminology Relating to Molecular Spectroscopy3. Significance and Use3.1 These test methods ar

8、e intended for quality controlacceptance of natural rubber and may be used for refereepurposes.4. Reagents4.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Anal

9、ytical Reagents of the American Chemical Society,where such specifications are available.4Other grades may beused, provided it is first ascertained that the reagent is ofsufficiently higher purity to permit its use without lessening theaccuracy of the determination.4.2 Purity of WaterUnless otherwis

10、e indicated, referencesto water shall be understood to mean reagent water conformingto Specification D 1193.5. Sampling5.1 A lot of natural rubber shall be sampled, the sampleprepared for test, and the acceptability of the lot determinedfrom tests on the sample in accordance with Test MethodsD 1485.

11、VOLATILE MATTER6. Procedure6.1 Weigh a 10 to 12-g specimen of homogenized rubber tothe nearest 1 mg and then dry it in a circulating-air oven at 1006 5C to constant mass. If it is suspected that volatilehydrocarbon oils are present, they should be determined by1These test methods are under the juris

12、diction of ASTM Committee D11 onRubber and are the direct responsibility of Subcommittee D11.22 on NaturalRubber.Current edition approved March 1, 2007. Published May 2007. Originallyapproved in 1953. Last previous edition approved in 2002 as D 1278 91a (2002)e1.2For referenced ASTM standards, visit

13、 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.3Withdrawn.4Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society,

14、 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.1Cop

15、yright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.heating the rubber in a circulating-air oven at 160 6 5C toconstant weight. The drying is facilitated by cutting the rubberinto 25-mm strips having a maximum width and thickness of2.5 by 1.

16、25 mm or by passing it through a laboratory mill witha clearance between rolls set at 0.5 6 0.1 mm (0.020 6 0.004in.). Keep the dried specimen in a covered weighing vessel orin a desiccator after its removal from the oven until it is readyto be weighed.7. Calculation7.1 Calculate the percentage of v

17、olatile matter as follows:V 5 1 2 B 3 D!/A 3 C!# 3 100 (1)where:V = percentage of volatile matter,A = mass of piece taken from bale,B = mass of piece after homogenizing,C = mass of specimen before oven drying, andD = mass of specimen after oven drying.8. Precision and Bias8.1 Task groups for the pur

18、pose of obtaining precision andbias data in accordance with Practice D 4483 are beingorganized and precision and bias statements will be added tothis test method when available.DIRT9. Apparatus9.1 SieveA 45-m (No. 325) sieve conforming to Speci-fication E11.10. Reagents10.1 Petroleum, Light, boiling

19、 between 60 and 80C.10.2 Rubber Peptizing Agent.NOTE 1The peptizing agent selection is not critical but, where one isused that contains inert mineral filler, the peptizer should be added to therubber solvent and filtered5prior to addition of the rubber.10.3 Rubber Solvent, Xylene, or a Hydrocarbon S

20、olvent,with a distillation range within 135 to 220C.11. Procedure11.1 Weigh a 10 to 12-g specimen of homogenized rubber tothe nearest 0.1 g and cut into pieces having a maximumdimension of less than 3 mm. Place the pieces in a 250-cm3conical flask and cover with 150 cm3of rubber solventcontaining ab

21、out 0.5 g of peptizing agent. Heat the mixture andmaintain it at a temperature of 125 to 130C (Note 2) untildissolution is complete (about 3 h).NOTE 2Overheating or boiling may cause gelling or charring. Infra-red heating lamps and magnetic stirring are aids that will induce rubbersolution.11.2 Pour

22、 the hot solution through a 45-m (No. 325) sievepreviously weighed to the nearest 0.1 mg. Rinse the flask threetimes with about 25 cm3of hot rubber solvent and pour therinsings through the sieve. Transfer any dirt remaining in theflask to the sieve by means of a jet of light petroleum and washthe di

23、rt on the sieve until free of rubber solution. Dry the sieveand contents at 100 6 5C and weigh to the nearest 0.1 mg.12. Calculation12.1 Calculate the dirt content as follows:D 5 C 2 B!/A 3 100 (2)where:D = percentage of dirt,A = mass of the specimen,B = mass of the clean, dry sieve, andC = mass of

24、the sieve plus dirt.13. Precision and Bias13.1 Task groups for the purpose of obtaining precision andbias data in accordance with Practice D 4483 are beingorganized and precision and bias statements will be added tothis test method when available.ASH14. Apparatus14.1 CrucibleAn unetched porcelain cr

25、ucible having acapacity of 50 cm3. If copper is subsequently to be determined,a smooth unetched silica crucible is preferred, but a Vycorcrucible or an ignited, acid-washed unetched No. 2 Coorsporcelain crucible may be used.NOTE 3In cases of dispute where the greatest accuracy is required,use a new,

26、 smooth silica crucible each time the test is run.14.2 Muffle Furnace, with temperature indicator and con-trol.14.3 Filter Paper, Ashless, about 150 mm in diameter.15. Procedure15.1 Weigha5to6-gspecimen of homogenized rubber tothe nearest 1 mg and place it in a crucible previously ignitedand weighed

27、 to the nearest 0.1 mg. Place the crucible and itscontents in a furnace controlled at a temperature of 550 6 25Cuntil free from carbon (Note 4). When ashing is complete, coolthe crucible in a desiccator and then weigh it to the nearest 0.1mg.NOTE 4The rubber may be charred over a small flame or on a

28、 hotplate before it is placed in the furnace. When the rubber is not previouslycharred before placing it in the furnace, the crucibles shall be placed on asuitable tray to permit placing them in the furnace simultaneously, and thedoor of the furnace shall then be kept closed for at least 1 h whilefl

29、ammable vapors are evolved. If copper, manganese, or iron is to bedetermined, the specimen shall be wrapped in a 150-mm ashless filterpaper previous to ashing.16. Calculation16.1 Calculate the ash content as follows:A 5 C 2 B!/D 3 100 (3)5The sole source of supply of the apparatus (Number 40 Watman

30、filter paper)known to the committee at this time is Fischer Scientific, 1600 W. Glenlake Ave.,Itasca, IL 60143. If you are aware of alternative suppliers, please provide thisinformation to ASTM International Headquarters. Your comments will receivecareful consideration at a meeting of the responsibl

31、e technical committee,1whichyou may attend.D 1278 91a (2007)2where:A = percentage of ash,D = mass of the specimen,B = mass of the empty crucible, andC = mass of the crucible plus ash.17. Precision and Bias17.1 Task groups for the purpose of obtaining precision andbias data in accordance with Practic

32、e D 4483 are beingorganized and precision and bias statements will be added tothis test method when available.COPPER(Referee Colorimetric Method)618. Apparatus18.1 PhotometerA spectrophotometer or a photoelectricphotometer with a band pass filter having maximum transmit-tance at about 435 nm. Matche

33、d absorption cells, 1 to 5 cm inpath length may be used, however, cells 2 to 5 cm in pathlength are preferred.NOTE 5For definitions of terms used in this procedure, refer toTerminology E 131. The cm unit is not a preferred submultiple of themetre but it is used by Committee E13 on Molecular Microsco

34、py. (SeeTerminology E 131).19. Reagents and Materials19.1 Carbon Tetrachloride (CCl4).19.2 Copper Sulfate, Standard Solution (1 cm3= 0.1 mgCu)Dissolve 0.393 g of copper sulfate (CuSO45H2O) inwater, add 3 cm3of concentrated sulfuric acid (H2SO4,density = 1.84 Mg/m3), and dilute to 1 cm3with water. Th

35、issolution should remain stable for at least a month.19.3 Copper Sulfate, Standard Solution (1 cm3= 0.01 mgCu)Dilute 10 cm3of the CuSO4solution (1 cm3= 0.1 mgCu) to 100 cm3with water. Make up this solution fresh eachday.19.4 Nitric Acid (1 + 2)Mix 1 volume of concentratednitric (HNO3, density = 1.42

36、 Mg/m3) with 2 volumes of water.19.5 Zinc Dibenzyldithiocarbamate Solution7Dissolve0.1 g of zinc dibenzyldithiocarbamate in 1 cm3of CCl4.NOTE 6The commercial grade of zinc dibenzyldithiocarbamate7isusually suitable for use as a reagent. Lower blanks and more rapidextractions, however, may be obtaine

37、d with the purified reagent.Amethodof preparation of pure reagent is available in the literature.620. Preparation of Calibration Curve20.1 Pipet 0, 1, 2, 3, and 4-cm3separate portions of standardCuSO4solution (1 cm3= 0.01 mg Cu) into separate separatoryfunnels. Add 5 cm3of HNO3(19.4) to each funnel

38、and diluteto about 100 cm3. With a pipet add 25 cm3of zinc diben-zyldithiocarbamate solution to each funnel if 2 to 5-cmabsorption cells are to be used, or 10 cm3of the solution if1-cm cells are to be used.20.2 Proceed with the extraction as described in 21.1 andmeasure the absorbance of the CCl4sol

39、ution as described in21.1, using the solution with no added copper as the referencesolution.20.3 Prepare a calibration curve by plotting the relationshipbetween copper concentration and absorbance. The calibrationcurve should be checked whenever necessary, depending onlocal conditions and on the typ

40、e of instrument used.21. Procedure21.1 Ash a 10-g specimen wrapped in filter paper inaccordance with Section 15. Ash a blank consisting of the filterpaper in the same manner and carry it through the procedure inthe same manner as the specimen. Add 10 cm3of HNO3(19.4)to the crucible and digest the mi

41、xture on a steam bath for 30min. Transfer the solution to a 100-cm3volumetric flask. Cooland dilute it to the 100-cm3mark with water. Pipet 50 cm3ofthe solution into a separatory funnel and dilute to about 100cm3with water. With a pipet add 25 cm3of zinc diben-zyldithiocarbamate solution if 2 to 5-c

42、m absorption cells are tobe used or add 10 cm3of the solution if the 1-cm cells are tobe used. Shake the mixture vigorously for 1 min, allow thelayers to separate, and draw off the CCl4layer through a funnelcontaining a plug of absorbent cotton, directly into the absorp-tion cell. Leave a small amou

43、nt of CCl4in the separatoryfunnel so as to avoid introducing water into the cell. If thereagents are sufficiently pure, this one extraction is sufficient.Each new reagent solution shall be tested. If a second succes-sive extraction removes additional copper, it will be necessaryto make additional ex

44、tractions and combine the extracts. In thiscase combine the extracts in a 50-cm3volumetric flask anddilute with the reagent to the 50-cm3mark.21.2 Measure the absorbance with a spectrophotometer at435 nm or, if a photoelectric photometer is used, by using theappropriate filter. Use the blank solutio

45、n as the referencesolution. Determine the concentration of copper in the testsolution from the absorbance reading and the calibration curve(20.3). Express the result in milligrams of copper per kilogramof rubber (parts per million).22. Precision and Bias22.1 Task groups for the purpose of obtaining

46、precision andbias data in accordance with Practice D 4483 are beingorganized and precision and bias statements will be added tothis test method when available.COPPER(Alternative Colorimetric Method)23. Apparatus23.1 See Section 18 and Note 4.24. Reagents and Materials24.1 Ammonium Hydroxide (density

47、 = 0.90 Mg/m3)Concentrated ammonium hydroxide (NH4OH).24.2 Chloroform (CHCl3).6Martens, R. I., and Githens, Sr., R. E., “Small Amounts of Copper in Dyes andRubber Chemicals,” Analytical Chemistry , Vol 24, 1952, pp. 9913. Reprinted inRubber Chemistry and Technology, Vol 26, 1953, pp. 257262.7The sol

48、e source of supply of this salt (trade name Arazate) known to thecommittee at this time is Uniroyal Chemical, Elm Street, Naugatuck, CT 06770. Ifyou are aware of alternative suppliers, please provide this information to ASTMInternational Headquarters. Your comments will receive careful consideration

49、 at ameeting of the responsible technical committee,1which you may attend.D 1278 91a (2007)324.3 Citric Acid Solution (33.33 %)Dissolve 50 g of citricacid in 100 cm3of water.24.4 Copper Sulfate, Standard Solution (1 cm3= 0.1 mgCu)See 19.2.24.5 Copper Sulfate, Standard Solution (1 cm3= 0.01 mgCu)See 19.3.24.6 Hydrochloric Acid-Nitric Acid MixtureMix 2 vol-umes of concentrated hydrochloric acid (HCl, density = 1.19Mg/m3) with 1 volume of concentrated nitric acid (HNO3,density = 1.42 Mg/m3) and 3 volumes of water.24.7 Sodium Sulfate, Anhyd