ASTM D6556-2016 5658 Standard Test Method for Carbon Black&x2014 Total and External Surface Area by Nitrogen Adsorption《碳黑的标准试验方法 采用氮吸附法测定碳黑总体和外部表面面积》.pdf

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1、Designation: D6556 16Standard Test Method forCarbon BlackTotal and External Surface Area by NitrogenAdsorption1This standard is issued under the fixed designation D6556; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of l

2、ast revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers the determination of the totalsurface area by the Brunauer, Emmett, and Teller (B.E.T. NSA)theo

3、ry of multilayer gas adsorption behavior using multipointdeterminations and the external surface area based on thestatistical thickness surface area method.1.2 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.3 This standard d

4、oes 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. (The minimumsafety equipment shou

5、ld include protective gloves, sturdy eyeand face protection).2. Referenced Documents2.1 ASTM Standards:2D1799 Practice for Carbon BlackSampling PackagedShipmentsD1900 Practice for Carbon BlackSampling Bulk Ship-mentsD3765 Test Method for Carbon BlackCTAB (Cetyltrim-ethylammonium Bromide) Surface Are

6、a (Withdrawn2007)3D4483 Practice for Evaluating Precision for Test MethodStandards in the Rubber and Carbon Black ManufacturingIndustries3. Summary of Test Method3.1 The total and external surface areas are measured byevaluating the amount of nitrogen adsorbed, at liquid nitrogentemperature, by a ca

7、rbon black at several partial pressures ofnitrogen. The adsorption data is used to calculate the NSA andSTSA values.4. Significance and Use4.1 This test method is used to measure the total andexternal surface area of carbon blacks based on multipointnitrogen adsorption. The NSA measurement is based

8、on theB.E.T. theory and it includes the total surface area, inclusive ofmicropores, pore diameters less than 2 nm (20 ). The externalsurface area, based on the statistical thickness method (STSA),is defined as the specific surface area that is accessible torubber.4.2 CTAB Surface Area (formerly Test

9、 Method D3765) hasbeen withdrawn. The CTAB value may be estimated from theSTSA value using Eq 1. The equation is based on a linearregression of the STSAand CTAB measured values of the SRB5 standards.CTAB 5 STSA*1.017012.6434 (1)5. Apparatus5.1 Multipoint Static-Volumetric Gas Adsorption Apparatus,wi

10、th Dewar flasks and all other accessories required foroperation.5.2 Sample Cells, that when attached to the adsorptionapparatus, will maintain isolation of the sample from theatmosphere equivalent to a helium leak rate of 1 L)Fill and cover the Dewar for aminimum of 16 h prior to use, unless continu

11、ous Pomeasure-ments are employed. For continuous Po, use a 2-h Dewarequilibration. Once equilibration is reached, a large Dewar canmaintain this equilibration for several days if kept filled andcovered. The cleaning frequency is left to the discretion of theoperator, but is not to exceed once per we

12、ek.9.3 Following is a list of Pomeasurement options:9.3.1 Continuous Po(measurement at each relative pressurepoint)This method is considered the best practice; however,it generally increases analysis time.9.3.2 Single PoPer AnalysisAlthough this value can bemeasured before, during, or after the run,

13、 a Povalue measuredat the end of the analysis is preferred, since STSAis calculatedfrom the last data points acquired and is significantly influ-enced by Povalues. This method requires that a Povalue bedetermined prior to initiating any measurements to ensureequilibrium of the Dewar as described in

14、9.4. Subsequently, anew Povalue is measured for each run, which is used forcalculating NSA/STSA values.9.3.3 Daily PoThis method is used when evidence of astable Dewar is present and no changes in atmospheric pressuregreater than 0.13 kPa (1 mm Hg) occur.9.3.4 Calculated PoThis method calculates a P

15、ovalue bymeasuring atmospheric pressure and adding a value between1.3 and 2.6 kPa (10 and 20 mm Hg). The operator isD6556 162responsible for determining the constant used in their labora-tory; however, 2.0 kPa (15 mm Hg) is most commonly used.9.4 With the exception of continuous Pomeasurements, it i

16、srecommended that the Povalue be determined prior to initiat-ing NSA/STSAanalyses.APovalue of 1.3 to 2.6 kPa (10 to 20mm Hg) above atmospheric pressure and two consecutive Povalues that differ by no more that 0.13 kPa (1 mm Hg) over a10-min time period are indications of a stable Dewar. Experi-ence

17、will teach the operator about expected differences in Poand atmospheric pressure in their laboratory.NOTE 4A minimum wait time of 10 min is recommended between Pomeasurements, as immersing the Pocell into the LN2 disrupts thetemperature equilibration. Pomeasurements taken at short intervals willresu

18、lt in erroneously high and unstable values.9.5 Determine the free space of the sample cell by measure-ment with helium or by calculation using an assumed carbonblack density of 1.9 g/cm3.9.6 Obtain a minimum of five data points evenly spaced inthe 0.1 to 0.5 relative pressure (P/Po) range. For some

19、treadcarbon blacks, particularly N100 and N200 series, it is neces-sary to measure two additional data points, 0.05 and 0.075, inorder to increase the accuracy of the NSAmeasurement.Adatapoint consists of the relative pressure of equilibrium and thetotal amount of nitrogen gas adsorbed by the sample

20、 at thatrelative pressure.9.7 Determine the mass of the cell with dry sample to thenearest 0.1 mg. This may be done before or after measuringnitrogen adsorption. Avoid inconsistent use of helium, as abuoyancy error of 1 mg/cm3of cell volume can occur. As analternative, the carbon black mass may be d

21、etermined directlyby pouring it from the sample cell into a tared weighing pan,taking care to remove all of the carbon black.10. Calculation10.1 Most automated instruments will perform the follow-ing computations at the completion of the analysis. The usermust verify that the internal computations c

22、onform to thefollowing method.10.2 Sample Mass:sample mass dried! 5 mass of cell1sample! 2 mass of cell! (2)Record masses to nearest 0.1 mg.10.3 Volume of Nitrogen Adsorbed:10.3.1 Calculate total volume of nitrogen adsorbed per gramof sample to the nearest 0.0001 cm3/g as follows:Va5Volume of Nitrog

23、en for each dosing in cm3sample mass in g(3)10.4 Nitrogen Surface Area:10.4.1 Determine the nitrogen surface area (NSA) using aB.E.T. plot from the Brunauer, Emmett, and Teller4equation asfollows:PVaPo2 P!51VmC1C 2 1VmC3PPo(4)where:P = manometer pressure in kPa,Po= saturation vapor pressure of nitro

24、gen in kPa,Vm= volume of nitrogen per gram that covers one mono-molecular layer in standard cm3/g, andC = B.E.T. constant. Its numerical value depends on theheat of adsorption of the monomolecular layer.10.4.2 Plot P/Poon the X-axis versusPVaPo2P!on theY-axis, for data sets having P/Poin the range o

25、f 0.05 to 0.30(linear region of B.E.T. equation).10.4.3 The data points (three or more) that give the beststraight line are used to calculate the slope and y-intercept. Theslope and y-intercept are used to calculate the surface area. Forexamples of how to select the proper relative pressure range,se

26、e Table 1.10.4.4 As an alternative, the interpretation of the properrelative pressure can generally be simplified by specifying thefollowing pressure ranges for the various carbon black types:BET RangeN300 and Carcass Grades 0.10.3N100 and N200 0.050.2Carbon Blacks 130 m2/g 0.050.1It is the responsi

27、bility of the operator to assure that theseguidelines are appropriate for their samples.10.4.5 A B.E.T. plot that yields a negative y-intercept couldbe indicative of the presence of micropores (2 nm diameter),but other factors can produce a negative y-intercept. Thesurface area is calculated from th

28、ree or more points within thepressure range that yields the highest correlation coefficientand a positive y-intercept.4Brunuaer, Emmett, and Teller, Journal of the American Chemical Society, Vol.60 , 1938, p. 309.TABLE 1 Example of NSA Data AnalysisN121ARaw Data CalculationP/PoVol. Ads.,cm3/gRel. Pr

29、ess.RangeCorrelationCoefficientNSA,m2/g0.0500 26.716 . . . . . . . . .0.1000 29.753 . . . . . . . . .0.1500 32.313 0.050.15 0.999981 123.90.2000 34.692 0.050.20 0.999992 124.00.2500 37.110 0.050.25 0.999990 123.60.3000 39.641 0.050.30 0.999935 122.8N326BRaw Data CalculationP/PoVol. Ads.,cm3/gRel. Pr

30、ess.RangeCorrelationCoefficientNSA,m2/g0.0500 16.675 . . . . . . . . .0.1000 18.318 . . . . . . . . .0.1500 19.859 0.050.15 0.999960 75.60.2000 21.426 0.050.20 0.999948 76.30.2500 23.035 0.050.25 0.999964 76.60.3000 24.751 0.050.30 0.999979 76.6N683BRaw Data CalculationP/PoVol. Ads.,cm3/gRel. Press.

31、RangeCorrelationCoefficientNSA,m2/g0.0500 8.194 . . . . . . . . .0.1000 9.113 . . . . . . . . .0.1500 9.945 0.050.15 0.999939 38.20.2000 10.739 0.050.20 0.999950 38.50.2500 11.543 0.050.25 0.999972 38.60.3000 12.364 0.050.30 0.999973 38.4AThe most accurate NSA is measured between 0.05 and 0.20 relat

32、ive pressure.BThe most accurate NSA is measured between 0.05 and 0.30 relative pressure.D6556 16310.4.6 Calculate the nitrogen surface area to the nearest 0.1m2/g as follows:Surface area m2/g! 5 Vm 34.35 (5)where:Vm =1B1MB = Y-axis intercept, 6105,M = slope of the straight line, 6105, and4.35 = area

33、 occupied by 1 cm3of nitrogen =6.02 31023!16.2 310220!224006.02 1023= Avogadros number,16.2 1020= area of nitrogen molecule in m2, and22400 = number of cm3occupied by one mole of gasat STP.10.5 Statistical Thickness Surface Area:10.5.1 Determine the STSA5of the black using a plot of thevolume of nit

34、rogen gas adsorbed per gram of sample at STP(Va) versus the statistical layer thickness (t).10.5.2 Prepare the Va-t plot by plotting t (nm) on the X axisversus Va(dm3/kg at STP) on the Y axis, for data sets havingP/Poequally spaced in the range of 0.2 to 0.5.where:t = statistical layer thickness of

35、carbon black =0.088(P/Po)2+ 0.645 (P/Po) + 0.298NOTE 5The carbon black thickness model was developed using anN762 carbon black in the P/Po range of 0.2 to 0.5. T values calculatedoutside of this range are invalid and will result in erroneous STSA values.10.5.3 Determine the slope of the Va-t plot us

36、ing standardlinear regression.10.5.4 Calculate the STSA to the nearest 0.1 m2/g asfollows:STSA 5 M 315.47 (6)where:M = slope of the Va-t plot, and15.47 = a constant for the conversion of nitrogen gas toliquid volume, and conversion of units to m2/g.10.5.5 STSAis based on a thickness model developed

37、usingan N762 carbon black. This carbon black was chosen becauseof its low surface area and low structure level. This universalmodel does not perfectly apply to all carbon blacks;consequently, while it is theoretically impossible for externalsurface area to be higher than total surface area, in pract

38、icethere are instances where STSA is higher than NSA. Foranalyses that yield STSA values that are higher than NSA, themeasured STSA value should be reported.11. Report11.1 Report the following information:11.1.1 Proper sample identification,11.1.2 Number of data points and relative pressures used to

39、obtain both NSA and STSA,11.1.3 The sample mass to the nearest 0.1 mg, and11.1.4 The NSAor STSA, or both, of the sample reported tothe nearest 0.1 m2/g.12. Precision and Bias12.1 These precision statements have been prepared inaccordance with Practice D4483. Refer to this practice forterminology and

40、 other statistical details.12.2 An Interlaboratory precision program (ITP) informa-tion was conducted as detailed in Table 2. Both repeatabilityand reproducibility represent short-term (daily) testing condi-tions. The testing was performed using two operators in eachlaboratory performing the test on

41、ce on each of two days (totalof four tests). A test result is the value obtained from a singledetermination. Acceptable difference values were not mea-sured. The between operator component of variation is in-cluded in the calculated values for r and R.12.3 Nitrogen Surface Area (NSA):12.3.1 A Type 1

42、 interlaboratory precision program wasconducted. Both repeatability and reproducibility representshort-term (daily) testing conditions. The testing was per-formed using two operators in each laboratory performing the5Magee, R. W., Rubber Chemistry and Technology, Vol. 68, No. 4, 1995, p. 590.TABLE 2

43、 SRB8 ITP InformationNumber of Labs (M/H/L)SRB8 Material Grade Producer Test PeriodD6556NSAD6556STSASRB-8A N326 Continental March 2008 58 (0/1/0) 54 (1/2/0)SRB-8A2 N326 Continental March 2013 67 (1/2/0) 63 (1/2/0)SRB-8B N134 Cabot June 2009 65 (0/3/1) 62 (2/2/2)SRB-8B2 N134 Cabot March/April 2014 11

44、 (1/1/0) 15 (1/1/0)SRB-8C HS Tread Columbian September 2010 63 (1/2/0) 58 (2/3/0)SRB-8D LS Carcass Cabot March 2009 64 (1/2/2) 60 (1/2/0)SRB-8E N660 Orion September 2008 54 (1/1/1) 51 (1/1/0)SRB-8F N683 Orion March 2010 67 (2/2/0) 64 (1/1/0)SRB-8F2 N683 Orion March 2015 30 (0/1/0) 44 (2/1/0)SRB-8GAN

45、990 Cancarb Last half of 1996 N/A N/AASRB-8G was produced and approved in the last half of 1996 as SRB-5G and has continued to be included in the current SRB sets since that time. At the time it wasproduced and approved it was D24s practice to only publish the within-laboratory standard deviation, S

46、r, and associated limits.The between-laboratory standard deviation,SR, was never published and since the data is no longer available it is not possible to calculate or publish the SR values and corresponding limits. The SRB G materialwas only tested for NSA, STSA, and OAN per the test method version

47、 available in 1996.D6556 164test once on each material on each of two days (total of fourtests). The number of participating laboratories is listed inTable 2.12.3.2 The results of the precision calculations for this testare given in Table 3. The materials are arranged in ascending“mean level” order.

48、12.3.3 RepeatabilityThe pooled relative repeatability, (r),of the NSAtest has been established as 1.1 %.Any other valuein Table 3 may be used as an estimate of repeatability, asappropriate. The difference between two single test results (ordeterminations) found on identical test material under there

49、peatability conditions prescribed for this test will exceed therepeatability on an average of not more than once in 20 casesin the normal and correct operation of the method. Two singletest results that differ by more than the appropriate value fromTable 3 must be suspected of being from different populationsand some appropriate action taken.NOTE 6Appropriate action may be an investigation of the test methodprocedure or apparatus for faulty operation or the declaration of asignificant difference in the two materials, samples, and so forth,

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