ASTM D3677-2010e1 Standard Test Methods for RubberIdentification by Infrared Spectrophotometry《分光光度法橡胶鉴定的标准试验方法》.pdf

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1、Designation: D3677 101Standard Test Methods forRubberIdentification by Infrared Spectrophotometry1This standard is issued under the fixed designation D3677; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision.

2、 A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1NOTEEditorially corrected 9.1.1 in October 2011.1. Scope1.1 Th

3、ese test methods cover rubber identification and arebased on infrared examination of pyrolysis products (pyrolyz-ates) and films.1.2 These test methods are applicable to rubbers in the rawstate and, when compounded, both in the cured and uncuredstate.1.3 Since it is customary in infrared spectrophot

4、ometry touse wavenumbers (cm1) rather than Hertz (Hz), the unit forfrequency in the SI system, the former is employed throughoutthis test method.1.4 This test method assumes that specimens and infraredspectra are prepared and analyzed by experienced personneland that the equipment is operated accord

5、ing to the manufac-turers direction for optimum performance. No details foroperation of infrared spectrophotometers are included in thistest method.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 st

6、andard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use. Specific precau-tionary statements are given in Section 17.2. Referenced Documents2.1 ASTM Standards:2D297 Test Methods for Rubber ProductsChemicalAnaly-sisD1418 Prac

7、tice for Rubber and Rubber LaticesNomenclatureD3452 Practice for RubberIdentification by Pyrolysis-Gas ChromatographyE168 Practices for General Techniques of Infrared Quanti-tative Analysis3. Significance and Use3.1 For research, development, and quality control pur-poses, it is advantageous to dete

8、rmine the composition ofrubbers in cured, compounded products.3.2 This test method provides such composition analysisutilizing an infrared technique.4. Reagents4.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall c

9、onform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.3Other grades may beused, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of

10、the determination.4.2 Acetone.4.3 Alcohol, ethanol, denatured.4.4 2-Butanone.4.5 Chloroform.4.6 Congo Red Paper.4.7 Diatomaceous Filter AidSome grades are quite unsat-isfactory in that they will not sufficiently absorb carbon black.4.8 1,2-DichlorobenzeneA check on suitability may bemade by evaporat

11、ing 50 cm3to dryness and making an infraredspectrum of the residue. Any substantial absorbance at posi-tions near those wavenumbers that will be used for rubberanalysis, indicates that the 1,2-dichlorobenzene is unsuitablefor use.4.9 Dry Compressed Air and Nitrogen, in cylinders, orprovided as a lab

12、oratory service.4.10 Sodium Sulfate, anhydrous.1These test methods are under the jurisdiction of ASTM Committee D11 onRubber and are the direct responsibility of Subcommittee D11.11 on ChemicalAnalysis.Current edition approved Feb. 1, 2010. Published March 2010. Originallyapproved in 1978. Last prev

13、ious edition approved in 2004 as D3677 00 (2004).DOI: 10.1520/D3677-10E01.2For 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

14、ASTM website.3Reagent 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 Stat

15、es Pharmacopeiaand National Formulary, U.S. Pharmaceutical Convention, Inc. (USPC), Rockville,MD.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.4.11 Toluene.TEST METHOD A QUALITATIVE ANALYSIS5. Scope5.1 This test method, based on in

16、frared examination ofpyrolysis products (pyrolyzates) and films, will identify therubbers in 6.1 occurring alone or in binary blends in the rangefrom 80 % major component to 20 % minor component.Exceptions to this will be found in 6.2.5.2 This test method is applicable to rubbers in the raw stateand

17、, when compounded, both in the cured and uncured state.5.3 This test method implies that sample preparation andinfrared spectrum are prepared and analyzed by experiencedpersonnel and that the equipment used for the production of thespectra is operated according to the manufacturers directionsfor opt

18、imum performance. No details for operation of infraredspectrophotometers are included in these test methods.6. Field of Application6.1 Infrared examinations of pyrolyzates and films willidentify mixtures of two of the following types of rubbers inthe range from 80 % major component to 20 % minor com

19、po-nent. (See the exceptions in 6.2.)6.1.1 Isoprene Rubbers (see 6.2.1):6.1.1.1 Natural rubber, synthetic polyisoprene, gutta percha,and balata are included.6.1.1.2 Examination of the pyrolyzate will not distinguishbetween the different forms of polyisoprene.6.1.1.3 Examination of a film will distin

20、guish natural andsynthetic polyisoprene from balata and gutta percha.6.1.2 Styrene-Butadiene Rubbers with Styrene Content ofApproximately 23.5 % Styrene (see 6.2.2):6.1.2.1 For the purpose of this standard, all copolymers ofstyrene and butadiene and their oil-extended forms are in-cluded.6.1.2.2 Exa

21、mination of the pyrolyzate will not distinguishbetween emulsion and solution polymerized rubbers.6.1.2.3 Examination of films may give some informationabout the monomer ratio and the polymerization system.6.1.3 Acrylonitrile-Butadiene Rubber with AcrylonitrileContent of Approximately 33 %:6.1.3.1 Ex

22、amination of the pyrolyzate will not measure theratio of acrylonitrile to butadiene.6.1.3.2 Examination of a film may give some informationabout the acrylonitrile content.6.1.4 Chloroprene RubberThis test method will not dis-tinguish between the different types of chloroprene rubbers.6.1.5 Butyl Rub

23、ber This test method will not distinguishbetween butyl rubber and its halogenated forms.6.1.6 Polybutadiene Rubber (High cis):6.1.6.1 Examination of the pyrolyzate will not distinguishbetween polybutadiene rubbers having different isomer ratios.6.1.6.2 Examination of a film may give some information

24、about the monomer ratio.6.1.7 Ethylene-Propylene Rubbers (see 6.2.3)This testmethod will not distinguish between rubbers having differentratios of ethylene to propylene nor between copolymers andterpolymers.6.2 Exceptions to the rubbers listed in 6.1 are:6.2.1 A blend of natural or synthetic isopren

25、e (20 %) andchloroprene (80 %), or both, may present difficulties, andidentification of the minor component may be achieved onlywhen its content is equal to or more than 30 % in the blend.6.2.2 A blend of butadiene-styrene rubber (80 %) and highcis polybutadiene rubber (20 %) may present difficultie

26、s, andidentification of the minor component may only be achievedwhen it is equal to or more than 30 % in the blend.6.2.3 Ethylene-propylene rubber in blends with other rub-bers presents difficulties when its content is in the range from20 to 40 %.6.3 In difficult cases, examination of the gaseous pr

27、oducts ofpyrolysis by gas chromatography (Practice D3452) may givefurther information.7. Summary of Test Method7.1 Identification from Pyrolyzates:7.1.1 A small quantity of extracted and dried rubber ispyrolyzed in a stream of nitrogen in a test tube held in a smallelectric, thermo-regulated furnace

28、 at 450 to 500C, or alterna-tively, rapidly pyrolyzed in a small test tube held in the hotzone of a gas flame.7.1.2 A test for chlorine is conducted during pyrolysis.7.1.3 A few drops of the pyrolyzate are transferred to a saltplate and an infrared spectrum recorded over the 4000 to 666cm1region.7.1

29、.4 The rubber is identified by comparison to standardreference spectra and by reference to a table of diagnosticabsorptions (significant absorption frequencies).7.1.5 Each laboratory employing this standard must preparespectra of all rubbers they might be expected to identify. Thesespectra must be p

30、repared in the same manner and using thesame equipment as will be used for unknown samples.7.2 Identification from Films:7.2.1 A small quantity of extracted and dried rubber isdissolved in 1,2-dichlorobenzene, filtered, and a film cast on asalt plate. This film is used as in 7.1.4.7.2.2 A small quan

31、tity of extracted and dried rubber issubjected to mild thermal degradation at 200 6 5C for a shorttime. The degraded sample is dissolved in trichloroethylenethen chloroform, and a film cast on a salt plate. This film isused as in 7.1.4.8. Apparatus8.1 Extraction Apparatus:8.1.1 The extraction appara

32、tus used shall be of the generaltype and dimensions shown in Fig. 1.D3677 10128.2 Test Tubes, small, and other necessary glassware suffi-cient to carry out the test as written.8.3 Pyrolysis Apparatus (Fig. 2)The pyrolysis apparatusconsists of a glass tube (P) having inward projections toprevent the

33、sample from falling to the bottom of the tube anda lateral condenser tube. The tube (P) has a ground-glassstandard taper (S) which carries a small glass adductor tube. Acollecting tube (T) is placed under the condenser tube. Anelectric, thermoregulated furnace (F) accommodates an alumi-num block (H)

34、 with holes for one or more tubes (P).8.4 Capillary Pipets.8.5 Oven, capable of maintaining a temperature of 200 65C for use in 10.2.8.6 Water Bath, for use in 10.2.8.7 Salt Plates, polished (sodium chloride or potassiumbromide), 4 by 25 mm, to serve as windows for the spectro-photometer.8.8 Infrare

35、d Spectrophotometer, High-Resolution Scanningor Fourier Transform, capable of recording a spectrum overthe 4000 to 667 cm1region. (High resolution4requires that thespectral slit width should not exceed 2 cm1over 80 % of thewavenumber range and at no place should it exceed 5 cm1.)Any spectrophotomete

36、r complying with these requirementsmay be used. The equipment shall be operated by an experi-enced analyst according to the manufacturers directions foroptimum performance.9. Preparation of Test Portion9.1 Temperature Controlled Pyrolysis in a Stream of Nitro-gen (Fig. 2; Preferred Method):9.1.1 Pre

37、pare the test portion by milling into a thin sheet ona laboratory mill or cutting into cubes about 2 mm wide andwrap approximately 0.5 g in filter paper or nylon cloth. Extractthe wrapped test portion in an extraction cup in accordancewith Section 19 of Test Methods D297, for a minimum of 4 hwith me

38、thanol, ethanol, or 2-propanol. A vulcanizate may beextracted with acetone or 2-butanone, in addition to the abovealcohols.Alternatively, the rapid reflux procedure may be usedfor1hinaccordance with Section 26 of Test Methods D297.9.1.2 Remove the extracted rubber from the apparatus anddry at 100C u

39、ntil free of solvent. One to two hours is usuallyrequired.9.1.3 Introduce a small amount of anhydrous sodium sulfateinto the collecting tube (T) to absorb water produced duringpyrolysis.9.1.4 Place a strip of moistened Congo red paper across themouth of the tube, as a test for chlorine (a change fro

40、m red toblue).9.1.5 If alternative chlorine determining methods are em-ployed, this procedure must be suitably modified.9.1.6 Bring the electrical furnace (F) to 450 to 500C andhold at this temperature. This range is recommended to obtainfast pyrolysis, without excessive degradation and carboniza-ti

41、on. Temperatures below this range should be avoided.9.1.7 Pass a slow stream of nitrogen through the pyrolysistube and introduce the tube into a hole of the aluminum block(H). The nitrogen serves to displace air, prevent oxidation, andfacilitate transfer of the pyrolysis products to the collectingtu

42、be (T).9.1.8 Carry on heating to complete distillation, which re-quires approximately 15 min.4High resolution is defined in “Specification for Evaluation of Research QualityAnalysis of Infrared Spectra,” Analytical Chemistry, ANCHA, Vol 47, No. 11, p.94A.FIG. 1 Extraction Apparatus with Glass Conden

43、serand Ground Glass JointF electric, thermoregulated furnaceH aluminum block, bored to hold tubesP glass tube for sample containerS ground-glass taperT collecting tubeFIG. 2 Temperature Controlled Pyrolysis ApparatusD3677 10139.1.9 Transfer a few drops of the pyrolyzate from the tube toa sodium chlo

44、ride or potassium bromide plate, using a capillarypipet.9.1.10 Place a spacer of suitable thickness in position, closethe cell with a second plate of the same material, and mount thecell in the infrared spectrophotometer.9.1.11 Record the spectrum over the wavelength range from4000 to 666 cm1.9.1.12

45、 Spectra should be obtained immediately after pyroly-sis to minimize further change in the pyrolysis products.9.2 Gas Flame Pyrolysis (Alternative Test Method):9.2.1 Prepare the extract, dry2goftest portion (9.1.1 and9.1.2), and place 0.1 to 0.2 g of the test portion in the bottomof a small glass te

46、st tube. Place a strip of moistened Congo redpaper across the mouth of the tube. Hold the tube horizontally,and quickly bring the lower end containing the test portion intothe hot zone of a gas burner, so that the rubber is rapidlypyrolyzed and charring is kept to a minimum. Note any colorchange in

47、the Congo red paper, from red to blue, indicating thepresence of chlorine.9.2.2 Maintain the heating until the pyrolyzate condenses inthe cool end of the tube, withdraw the test tube from the flame,and cool while holding horizontally.9.2.3 Alternatively, the sample may be placed in a smallglass tube

48、 and the end of the tube drawn out to a “retort” shapewith a blast lamp. Pyrolysis is carried out as described in 9.2.1.Care should be taken to keep the delivery end of the pyrolysistube warm enough so that pyrolysis products do not condenseand block the opening, causing the tube to explode. Thecond

49、ensate can be collected in a small test tube containinganhydrous sodium sulfate to remove moisture. Proceed as in9.1.9-9.1.12.9.2.4 If alternative chlorine detecting methods are em-ployed, this procedure must be suitably modified.10. Sample Preparation for Films10.1 Dissolution for Vulcanizates:10.1.1 Prepare a test portion in accordance with 9.1.1 and9.1.2.10.1.2 Pyrolyze and test for chlorine in accordance with9.1.4 and 9.1.5 or 9.2.1-9.2.4.10.1.3 Place1goftheprepared rubber (9.1.1 and 9.1.2) and50 cm3of 1,2-dichlorobenzene in a 100-cm3flask fitted