ASTM D2663-2008 Standard Test Methods for Carbon Black&x2014 Dispersion in Rubber《橡胶中碳黑分散度的标准试验方法》.pdf

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1、Designation: D 2663 08Standard Test Methods forCarbon BlackDispersion in Rubber1This standard is issued under the fixed designation D 2663; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number in pare

2、ntheses 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 degree of dispersion ofcarbon black in rubber. Three test methods are described asfollows:SectionsTest Method AVisual I

3、nspection 3-11Test Method BAgglomerate Count 12-23Test Method CMicroroughness Measurementwith Profilometer 24-34Test Method DMicroroughness Measurement with IFM 35-431.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3 This s

4、tandard 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 and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.

5、1 ASTM Standards:2D 3182 Practice for RubberMaterials, Equipment, andProcedures for Mixing Standard Compounds and Prepar-ing Standard Vulcanized SheetsD 4483 Practice for Evaluating Precision for Test MethodStandards in the Rubber and Carbon Black ManufacturingIndustries2.2 ASTM Adjuncts:Carbon Blac

6、k Dispersion Standards3Carbon Black Dispersion Chart4TEST METHOD AVISUAL INSPECTION3. Scope3.1 Test Method A is a qualitative visual test method.Ratings are made against a set of standard photographs (Fig.1),3and the results are expressed on a numerical scale.This testmethod cannot be used for compo

7、unds that contain fillers otherthan carbon black.4. Summary of Test Method4.1 The compound rubber is torn or cut to expose a freshsurface for examination by the eye, aided preferably by a handlens or a low-power binocular microscope. The dispersionlevel of the carbon black is compared against a seri

8、es of fivephotographic standards and then rated numerically from 1(very low) to 5 (high) (see Fig. 1).5. Significance and Use5.1 Visual dispersion ratings correlate with certain impor-tant physical properties of the compound. A rating of 5indicates a state of dispersion developing near maximumproper

9、ties, while a rating of 1 would indicate a state ofdispersion developing considerably depressed properties. Nor-mally, the visual dispersion ratings indicate the followinglevels of compound quality:Visual Dispersion Rating Classification4to5 High3 to 4 Intermediate2to3 Low1 to 2 Very low6. Apparatus

10、6.1 Sharp Knife or Razor Blade.6.2 Hand Lens (103) or binocular microscope (10 to 203).6.3 Illuminator, microscopical-type.6.4 Knife Heater.6.5 Series of Photographic Standards, rating 1 to 5. Thesestandards give the following percent dispersion ratings by theAgglomerate Count Method:1These test met

11、hods are under the jurisdiction of ASTM Committee D24 onCarbon Black and are the direct responsibility of Subcommittee D24.71 on CarbonBlack Testing in Rubber.Current edition approved Jan. 1, 2008. Published February 2008. Originallyapproved in 1967. Last previous edition approved in 2006 as D 2663

12、06.2For 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.3Available from ASTM International Headquarters. Order Adj

13、unct No.ADJD266302. Original adjunct produced in 1967.4Available from ASTM International Headquarters. Order Adjunct No.ADJD266301. Original adjunct produced in 1967.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.Visual Rating Black

14、 Dispersed, %170283914965997. Test Specimen7.1 Vulcanized CompoundsUse a slab of rubber about2 mm in thickness. Tear it so that a fresh surface is exposed.The tear may be initiated by a small cut. The most nearly flatpart of the tear is used for rating.7.2 Unvulcanized CompoundsUnvulcanized rubber m

15、aybe examined as follows:7.2.1 If the specimen contains curing agents, sheet it out andcure in a press to form a vulcanized slab about 2 mm inthickness. Mill and cure in accordance with Practice D 3182.Then proceed as in 7.1.FIG. 1 Carbon Black Dispersion StandardsVisual Analysis of Torn Vulcanizate

16、sD26630827.2.2 If the specimen contains no curatives, add the appro-priate materials with a minimum of mixing. Then cure andproceed as above.7.2.3 If the specimen contains no curatives and a dispersionevaluation with no further mixing is required, the compoundmust first be compressed to remove most

17、of the air holes. Toaccomplish this, press the rubber into a slab between thinsheets of plastic in a mold at a pressure of about 1.03 kPa for5 min at 105C. Care should be taken to avoid excessive flowduring this step. The surface to be examined is formed with asmooth cutting stroke using a sharp, ho

18、t knife (a standard typeknife heater may be employed). The most nearly smooth andflat part of the cut surface is used for rating.8. Number of Tests8.1 Preferably more than one test (on different tears) shouldbe made for each specimen. If convenient, more than oneoperator should rate the samples.9. P

19、rocedure9.1 Examine the prepared specimens under a hand lens orbinocular microscope (the latter being preferred), with obliqueillumination to accentuate surface detail. Keep the magnifica-tion and lighting conditions constant for all specimens.9.2 Compare the size and frequency of carbon agglomerate

20、sin the specimens (showing up as surface bumps or depressions)to the photographic standards. Then assign the most closelymatched numerical rating to each compound being rated. Inborderline cases, use fractional ratings, for example, 312 wouldindicate a rating between 3 and 4. In cases of dissimilari

21、ty inthe size and frequency of the agglomerates in the specimen andthose of the standards, the operator shall assign the rating thatin his judgment is most applicable. Certain compounds (forexample, NR and IR) are particularly prone to very small blackagglomerations which are difficult to resolve by

22、 the VisualInspection Method. In instances of high agglomerate fre-quency, the surface of stocks of this type may show a generalroughness or fine pebbled appearance. Differences are bestresolved at somewhat higher magnification (for example, 203,binocular microscope). If at all possible, examine com

23、poundsof this type also by the agglomerate count method, at least untilsufficient experience is gained to recognize dispersion differ-ences with the Visual Inspection Method.9.3 In comparing a series of different compounds, it is alsodesirable to rate the specimens side by side rather than one ata t

24、ime. This use of a control compound is also advisable. Thisis best prepared by individual operators, since dispersionrequirements may vary greatly for different types of com-pounds. The control sample should represent a minimumacceptable dispersion level for the type of compound beingrated. Because

25、it can be observed side by side with unknownsamples under identical conditions, a control compound ismore accurate than the photographic standards in discerningsmall deviations from what is considered the norm for aspecific type of compound. Prepare a fresh surface on thecontrol as often as necessar

26、y to ensure cleanliness.10. Report10.1 Ratings:10.1.1 List all ratings, including those on any controlcompound, on the basis of the 1 to 5 scale defined by thestandard photographs. Use fractional ratings when necessary.10.1.2 Average the ratings on different specimens of thesame compound as well as

27、the ratings of different operators.Report the final average values.10.2 Compound Identification:10.2.1 FormulationWhenever possible list the following:10.2.1.1 Carbon black, type and loading,10.2.1.2 Other fillers, type and loading,10.2.1.3 Polymer type, and10.2.1.4 Extender oil, type and loading.10

28、.2.2 MixingDescribe the mixing of the compound interms of one or more of the following:10.2.2.1 Standard mixing procedure,10.2.2.2 Type of equipment,10.2.2.3 Masterbatch,10.2.2.4 Finished compound (vulcanized), and10.2.2.5 Finished compound (unvulcanized).11. Precision and Bias11.1 No statement is m

29、ade about either the precision or thebias of Test Method A since the result is qualitative and notapplicable to statistical treatment.TEST METHOD BAGGLOMERATE COUNT12. Scope12.1 Test Method B is a quantitative test method. Dispersionis evaluated by measuring with a light microscope the percent-age a

30、rea covered by black agglomerates in microtomed sec-tions of the compound. Since this test method involves directmeasurement, it is quantitative and more accurate than thevisual test method. The test is applicable to the analysis ofcarbon black dispersion in compounds that contain other fillers.13.

31、Summary of Test Method13.1 The compounded rubber is microtomed into sectionssufficiently thin to permit observation of the carbon agglom-erates by transmitted light, with the aid of a light microscope.The total cross-sectional area of all agglomerates 5 m orlarger is counted, and from the known cont

32、ent of carbon blackin the stock, the percentage of carbon black below the 5-msize is calculated and expressed as “Percentage of CarbonBlack Dispersed.”14. Significance and Use14.1 Certain important physical properties of the compoundare influenced significantly by the degree of carbon blackdispersio

33、n within the compound (for example, tensile strengthand abrasion resistance). The correlation of these propertieswith the percentage dispersion determined by the AgglomerateCount Method approximates the following pattern for manytypes of black loaded rubber compounds:Dispersion, % ClassificationAbov

34、e 99 Very high97 to 99 High95 to 97 Intermediate92 to 95 LowD2663083Below 92 Very low15. Apparatus15.1 MicrotomeA sledge-type microtome equipped withspecimen clamp and holder for glass knives. Steel knives mayalso be employed, according to the preference of the operator.15.2 Freezing Blocks, consist

35、ing of a brass screw which isthreaded into an insulating block of TFE-fluorocarbon (Fig. 2).The TFE-fluorocarbon block shall be 28-mm square in crosssection and 40-mm high. The threaded part of the brass screwshall be 15 mm in diameter and shall extend into the center ofthe TFE-fluorocarbon block to

36、 a depth of 34 mm. Coarse,expansion-type threads should be used to prevent splitting ofthe TFE-fluorocarbon when the mount is frozen. The head ofthe brass screw shall be 18 mm in diameter and shall extend3 mm above the TFE-fluorocarbon insulator. The top of thescrew head shall be cross-hatched with

37、fine grooves to a depthof about 1 mm.15.3 MicroscopeAn optical microscope with binocularviewing (trinocular type if photomicrographs are desired) isrecommended. This should include a movable specimen stageand white light source with variable intensity. Lenses shouldinclude two 103 wide field eyepiec

38、es and objectives in therange from 6 to 103. Taking into account microscope tubecorrections, objectives should be selected so that magnifica-tions in the range from 75 to 1003 are available. (Forphotomicrographs a 43 plane objective and a 103 periplanaticeyepiece are recommended.)15.4 Microscope Acc

39、essoriesA 103 wide field eyepiececontaining a graticule that is 1 cm2in size and divided into10 000 small squares.15.5 Measuring LensA 73 measuring magnifier cali-brated down to 0.1 mm for measuring the swelling factor of themicrotome sections. A mechanical vernier stage can also beused for this pur

40、pose.15.6 Glass Pliers and CutterWide-face glazier pliers anda wheel-type glass cutter are recommended for preparing glassknives.15.7 Sample DieTempered steel die for cutting out 3 by8-mm specimens.15.8 Sable Brushes (00).15.9 Dewar Flask, 2dm3(2-L) size (wide-mouth).15.10 Glass KnivesThe knives are

41、 prepared from 50-mmwide strips of approximately 6-mm thick plate glass.15.11 Microscope Slides and Cover Glasses.16. Reagents and Materials16.1 Liquid Nitrogen.16.2 Water-Soluble Mucilage.16.3 Naphtha, boiling point range from about 113 to 144C.16.4 Xylene, boiling point range from 135 to 145C.17.

42、Sampling17.1 VulcanizatesSpecimens may be cut from standardtest sheets (about 2-mm thick) or from pieces of actual curedarticles. Vulcanized samples must be employed because of thesolvent used to uncurl the thin sections. If pieces other than2-mm sheets are used, they should first be cut down to ath

43、ickness of about 2 to 3 mm.17.2 Unvulcanized CompoundsFor rubbers of high unsat-uration (for example, OE-SBR, NR, and BR), dust small bits(enough subsequently to form buttons about 10 mm in diameterand about 2 to 3-mm deep) thoroughly with dicumyl peroxide.Cure in a button mold5under high pressure a

44、t about 155C.OE-SBR rubbers require about 30 to 60-min cure. BR requiresabout 10 to 15-min cure. After cure, scrape off the excessperoxide from the sample surface and proceed with sectioningin the standard manner, taking care not to pare down below thecured surface layer.17.2.1 For IIR, satisfactory

45、 surface cures can be obtainedwith a mixture of 1 part tetramethylthiuram disulfide (TMTD),1 part mercaptobenzothiazole (MBT), 1 part sulfur, and 5 partszinc oxide, with a cure of 1 h at 155C. Other alternativeapproaches for curing high unsaturation polymers withoutactually mixing in curatives are (

46、1) high-energy radiation and(2) chemical treatment with sulfur monochloride. However,before using either of these latter methods, the stock should bepressed out to eliminate most of the air holes. Cure inaccordance with Practice D 3182.18. Test Specimen18.1 Cut out a rectangular specimen 8-mm long,

47、3-mmwide, and approximately 2-mm deep. Use a cutting die, ifavailable. If a die is not used, the specimen length and widthshould be recorded using a measuring magnifier.18.2 Prepare one specimen block for each different com-pound to be examined.19. Preparation of Glass Knives19.1 Standard types of p

48、late glass are suitable for makingknives. Thickness should be preferably about 6 mm. A largesheet of glass should first be repeatedly broken in half so thatit eventually is in 50-mm wide strips. Fracture in this manneris preferred over simply breaking off 50-mm sections one at atime. Uneven strains

49、are encountered in the latter procedure,and irregularities may occur on the side faces on which theknife edge will be formed. Prior to fracture, it is also importantthat the glass be free of dirt. A wash in a liquid detergent isgenerally advisable.5A special mold containing several circular cavities that are approximately10 mm in diameter and 3 mm deep.FIG. 2 Brass Sample Mount and TFE-Fluorocarbon InsulatorD266308419.2 Using a fairly thick straightedge, score a straight line(perpendicular to the side faces) across the glass strip, 50 mmfrom the end. Ta