ASTM D3346-2007 Standard Test Methods for Rubber Property-Processability of Emulsion SBR (Styrene-Butadiene Rubber) With the Mooney Viscometer (Delta Mooney)《橡胶特性的标准试验方法 用莫氏粘度计(德尔塔.pdf

《ASTM D3346-2007 Standard Test Methods for Rubber Property-Processability of Emulsion SBR (Styrene-Butadiene Rubber) With the Mooney Viscometer (Delta Mooney)《橡胶特性的标准试验方法 用莫氏粘度计(德尔塔.pdf》由会员分享，可在线阅读，更多相关《ASTM D3346-2007 Standard Test Methods for Rubber Property-Processability of Emulsion SBR (Styrene-Butadiene Rubber) With the Mooney Viscometer (Delta Mooney)《橡胶特性的标准试验方法 用莫氏粘度计(德尔塔.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 3346 07Standard Test Methods forRubber PropertyProcessability of Emulsion SBR (Styrene-Butadiene Rubber) With the Mooney Viscometer (DeltaMooney)1This standard is issued under the fixed designation D 3346; the number immediately following the designation indicates the year oforiginal

2、adoption or, in the case of revision, the year of 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 explain the use of the shearing diskviscometer t

3、o obtain an indication of the processability ofnon-pigmented emulsion styrene-butadiene rubbers (SBR).They may also be used to separate those polymers that are easyto process from those that are difficult to process within a groupof polymers of the same type.1.2 The values stated in SI units are to

4、be regarded as thestandard. The values given in parentheses are for informationonly.1.3 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 and health practices and

5、 determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D 1646 Test Methods for RubberViscosity, Stress Relax-ation, and Pre-Vulcanization Characteristics (Mooney Vis-cometer)D 3182 Practice for RubberMaterials, Equipment, andProcedures for Mix

6、ing Standard Compounds and Prepar-ing Standard Vulcanized SheetsD 3896 Practice for Rubber From Synthetic SourcesSamplingD 4483 Practice for Evaluating Precision for Test MethodStandards in the Rubber and Carbon Black ManufacturingIndustries3. Terminology3.1 Definitions:3.1.1 D Mooney, nthe differen

7、ce in Mooney viscosityrecorded for a rubber at specified times during a test.3.1.2 Mooney viscosity, narbitrary measure of the viscos-ity of a rubber determined in a Mooney shearing disk viscom-eter, indicated by the torque required to rotate the diskembedded in a rubber specimen and enclosed in the

8、 die cavityunder specified conditions.4. Summary of Test Methods4.1 In Test Method A, the difference in Mooney viscosity at100C (212F) is determined at two specified times. Eithermassed or unmassed samples may be used.4.2 In Test Method B, the Mooney viscosity difference forunmassed samples is deter

9、mined between the minimum re-corded directly after starting the rotor and the subsequentmaximum (see Fig. 1).5. Significance and Use5.1 These empirical tests have been found to be suitable forranking a series of unpigmented emulsion SBR in order ofprocessability. They may also be used for comparing

10、a produc-tion lot with a standard of known processability characteristics.The difference between Mooney viscosities at two specifiedtimes will rank those emulsion SBR polymers that differappreciably in this property according to their processability.The actual values obtained for a given polymer dep

11、end onwhether or not the sample was massed, and may vary betweenlaboratories or with the type of machine used, and with thespecified times at which Mooney viscosity values were taken.6. Apparatus6.1 The apparatus shall be in accordance with theApparatussection of Test Methods D 1646.6.2 The large ro

12、tor shall be used.7. Sample Preparation7.1 For sampling procedure, refer to Practice D 3896.1These test methods are under the jurisdiction of ASTM Committee D11 onRubber and are the direct responsibility of Subcommittee D11.12 on ProcessabilityTests.Current edition approved Nov. 1, 2007. Published N

13、ovember 2007. Originallyapproved in 1974. Last previous edition approved in 2003 as D 3346 03.2For 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

14、 Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.7.2 Condition the sample until it has reached room tempera-ture of 23 6 3C (73 6 5.4F) throughout.7.3 The tests can be performed using specimens taken f

15、romeither massed or unmassed samples.7.3.1 To mass a sample, pass 250 6 5 g of the samplebetween the rolls of the standard laboratory mill described inPractice D 3182. The mill shall have a roll temperature of 50 65C (122 6 9F) and a distance between the rolls of 1.4 6 0.1mm (0.055 6 0.005 in.) as d

16、etermined by a lead slug.Immediately fold the sample in half and insert the folded endinto the mill for a second pass. Repeat this procedure until atotal of nine passes have been completed. Immediately insertthe rubber without folding into the mill for a tenth pass. Do notallow the sample to rest be

17、tween passes or to band on the millrolls at any time.7.3.2 Allow the massed samples to rest at room temperaturefor at least 30 min before preparing the specimens andmeasuring their viscosity.7.4 Condition unmassed samples until they have attainedroom temperature throughout before preparing the speci

18、mensand measuring their viscosity.8. Test Temperature8.1 The test temperature shall be 100 6 0.5C (212 6 9F).For a description of a suitable temperature-measuring system,refer to 6.1.3 of Test Methods D 1646.9. Calibration of Viscometer9.1 Calibrate the shearing disk viscometer in accordancewith the

19、 Calibration section of Test Methods D 1646.10. Specimen Preparation10.1 The test specimen shall consist of two pieces of thematerial being tested having a combined volume of25 6 3cm3. This volume is approximately 1.67 times thevolume of the test cavity when the large rotor is used, andensures that

20、the cavity is completely filled. For convenience themass of the test specimen of correct volume may be calculatedas follows:m 5 v 3 d 5 25 cm33 d (1)where:m = mass, g.v = volume in cm3=25cm3, andd = density in Mg/m3(g/cm3).NOTE 1Mg/m3and g/cm3are numerically equivalent.10.2 The test specimen pieces

21、shall be cut from the preparedsample and shall be of such dimensions that they fit within thedie cavity without projecting outside it before the viscometer isclosed.A45-mm (1.75-in.) diameter cutting die may be used toassist in preparing the test pieces. If necessary, it is permittedto stack layers

22、of mill-massed or unmassed sheets to achieve athickness of approximately 10 mm prior to cutting the testspecimen pieces.Ahole punched in the center of one of the testpieces facilitates the centering of the rotor stem. It shall not bepermissible to slip the test piece around the rotor stem bycutting

23、it edgewise. The test specimen shall be as free of air asit is practical to make it and shall be free of pockets which maytrap air against the rotor and die surfaces.11. Procedure11.1 Measure the viscosity in accordance with the Proce-dure section of Test Methods D 1646, Part A. The duration ofthe t

24、est shall include a 1 min preheat followed by 15 min formassed samples and 7 min for unmassed samples.11.2 Use the large rotor.11.3 Use a rotor speed of 0.21 6 0.002 rad/s (2.0 6 0.02r/min).11.4 Test Method AWhen the difference between Mooneyviscosity at two specified times is required, calculate as

25、follows:ML 15 min ML 1.5 min for massed samples, orML 7 min ML 1 min for unmassed samples.11.4.1 Negative numbers that are large in magnitude indi-cate good processability for the polymers tested.11.5 Test Method BWhen the difference required is be-tween the minimum viscosity recorded and the subseq

26、uentmaximum viscosity, calculate as follows:MLmax MLminwhere:MLmin= minimum viscosity reached shortly after startingthe rotor, andMLmax= subsequent maximum viscosity.11.5.1 The smaller the magnitude of MLmax MLmin, thebetter the processability for the polymers tested.11.5.2 When MLmax MLmin(see Fig.

27、 1) is used as ameasure of processability, readings must be taken at a mini-mum of 5 s intervals during the period when viscosity is risingafter a rapid initial fall. The use of a recording device capableof following the complete viscosity-time curve is recom-mended.11.6 The same processability rank

28、ing is obtained for a seriesof rubbers using specimens cut directly from the slab, or usingmassed samples as long as the same procedure is usedthroughout the series of viscosity tests.FIG. 1 Typical Mooney versus Time Curve for Processability Testof SBRD 3346 07212. Report12.1 The report on the proc

29、essability shall include thefollowing information for the rubber(s) under test and for areference sample:12.1.1 Identification of the sample tested,12.1.2 Method of sample preparation,12.1.3 Temperature of test and point of measurement exceptfor referee purposes where the complete temperature-timecu

30、rve shall be provided together with a description of themethod of measurement,12.1.4 Type of dies used, and12.1.5 Time in minutes for which the specimen is permittedto warm up before starting the rotor.12.1.6 Test Results:12.1.6.1 Test Method A:ML 15 min ML 1.5 min for massed sample, orML 7 min ML 1

31、 min for unmassed sample.12.1.6.2 Test Method B:MLmaxMLmin(for unmassed sample).13. Precision and Bias313.1 This precision and bias section has been prepared inaccordance with Practice D 4483. Refer to Practice D 4483 forterminology and other statistical calculation details.13.2 The precision result

32、s in this precision and bias sectiongive an estimate of the precision of these test methods with thematerials (rubbers) used in the particular interlaboratory pro-gram as described below. The precision parameters should notbe used for acceptance/rejection testing of any group ofmaterials without doc

33、umentation that they are applicable tothose particular materials and the specific testing protocols thatinclude these test methods.13.3 A Type 1 (interlaboratory) precision was evaluated in1989. Both repeatability and reproducibility are short term; aperiod of a few days separates replicate test res

34、ults.Atest resultis the value, as specified by these test methods, obtained on onedetermination of the property in question.13.4 For Test Method A, both massed and unmassed, threematerials (rubbers) were tested in six laboratories. For TestMethod B, two materials (rubbers) were tested in six labora-

35、tories. For both Test Methods A and B all materials (rubbers)were tested on two separate days.13.5 The results of the precision calculations for repeatabil-ity and reproducibility are given in Table 1, in ascending orderof material average or level, for each of the materials evalu-ated, and for each

36、 test method.13.6 The precision of these test methods may be expressedin the format of the following statements that use an appropri-ate value of r, R,(r), or (R), to be used in decisions about testresults. The appropriate value is that value of r or R associatedwith an average level in Table 1 clos

37、est to the average levelunder consideration at any given time, for any given material inroutine testing operations.13.7 RepeatabilityThe repeatability, r, has been estab-lished as the appropriate value tabulated in Table 1. Two singletest results, obtained under normal test method procedures, thatdi

38、ffer by more than this tabulated r (for any given level) mustbe considered as derived from different or nonidentical samplepopulations.13.8 ReproducibilityThe reproducibility, R, has been es-tablished as the appropriate value tabulated in Table 1.Twosingle test results obtained in two different labo

39、ratories, undernormal test method procedures, that differ by more than thetabulated R (for any given level) must be considered to havecome from different or nonidentical sample populations.13.9 Repeatability and reproducibility expressed as a per-centage of the mean level, (r) and (R), have equivale

40、ntapplication statements as above for r and R. For the (r) and (R)statements, the difference in the two single test results isexpressed as a percentage of the arithmetic mean of the two testresults.3Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting R

41、esearch Report RR: D11-1005.TABLE 1 Type 1 PrecisionNOTESr = Repeatability standard deviation, in measurement units,r = Repeatability, in measurement units,(r) = Repeatability, (relative) percent,SR = Reproducibility standard deviation, in measurement units,R = Reproducibility, in measurement units,

42、 and(R) = Reproducibility, (relative) percent.Material Average LevelWithin Laboratory Between LaboratoriesSr r (r)ASR R (R)APart 1Test Method AMassedRubber 3 23.5 0.89 2.52 10.7 1.26 3.56 15.1Rubber 2 15.4 0.81 2.30 14.9 1.28 3.62 23.4Rubber 1 11.9 0.82 2.32 19.4 1.61 4.56 38.3Part 2Test Method AUnm

43、assedRubber 3 9.8 0.42 1.18 12.0 0.73 2.08 21.2Rubber 2 1.1 0.79 2.24 (208) 0.79 2.24 (208)Rubber 1 2.8 0.46 1.31 46 0.70 1.99 70.0Part 3Test Method BUnmassedRubber 2Rubber 11.483.190.0790.560.221.5915.149.70.390.601.111.7075.253.3ASee discussion in 13.10 on (r) and (R).D 3346 07313.10 When the aver

44、age level or value of any measuredproperty approaches zero, the value of (r) and (R) mayapproach very large values depending on the general degree ofprecision of the test method. This should be kept in mind inreviewing Table 1.13.11 BiasIn test method terminology, bias is the differ-ence between an

45、average test value and the reference (or true)test property value. Reference values do not exist for these testmethods, since the value of the test property is exclusivelydefined by the test methods. Bias therefore cannot be deter-mined.14. Keywords14.1 D Mooney; Mooney; processability; SBR; styrene

46、-butadiene rubber; viscosityASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infr

47、ingement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standa

48、rd or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your vie

49、ws known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org).D 3346 074