ASTM D6556-2007 Standard Test Method for Carbon Black-Total and External Surface Area by Nitrogen Adsorption《炭黑的标准试验方法 用氮吸收法测定总的和外部表面积》.pdf
《ASTM D6556-2007 Standard Test Method for Carbon Black-Total and External Surface Area by Nitrogen Adsorption《炭黑的标准试验方法 用氮吸收法测定总的和外部表面积》.pdf》由会员分享,可在线阅读,更多相关《ASTM D6556-2007 Standard Test Method for Carbon Black-Total and External Surface Area by Nitrogen Adsorption《炭黑的标准试验方法 用氮吸收法测定总的和外部表面积》.pdf(5页珍藏版)》请在麦多课文档分享上搜索。
1、Designation: D 6556 07Standard Test Method forCarbon BlackTotal and External Surface Area by NitrogenAdsorption1This standard is issued under the fixed designation D 6556; 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 This test method covers the determination of the totalsurface area by the Brunauer, Emmett, and Teller (B.E.T. NSA)t
3、heory 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 standar
4、d 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. (The minimumsafety equipment s
5、hould include protective gloves, sturdy eyeand face protection).2. Referenced Documents2.1 ASTM Standards:2D 1799 Practice for Carbon BlackSampling PackagedShipmentsD 1900 Practice for Carbon BlackSampling Bulk Ship-mentsD 3765 Test Method for Carbon BlackCTAB (Cetyltrim-ethylammonium Bromide) Surfa
6、ce Area3D 4483 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 carbon blac
7、k 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 on theB.E
8、.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 Method D
9、 3765) 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 * 1.0170 1 2.6434 (1)5. Apparatus5.1 Multipoint Static-Volumetric Gas Adsorption Apparatus,with D
10、ewar 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 continuous
11、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 week.9
12、.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, a P
13、ovalue measuredat the end of the analysis is preferred, since STSA is 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 9.4
14、. 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 Pova
15、lue bymeasuring atmospheric pressure and adding a value between1.3 and 2.6 kPa (10 and 20 mm Hg). The operator isresponsible 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 isrecommended
16、 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 will teach t
17、he operator about expected differences in Poand atmospheric pressure in their laboratory.NOTE 2A 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 willresult in errone
18、ously high and unstable values.D65560729.5 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 trea
19、dcarbon 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 at
20、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 deter
21、mined 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 confo
22、rm to thefollowing method.10.2 Sample Mass:sample mass dried!5mass of cell 1 sample! 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 Nitrogen for
23、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:PVaPoP!51VmC1C1VmC3PPo(4)where:P = manometer pressure in kPa,Po= saturation vapor pressure of nitrogen in kPa,V
24、m= 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 versusPVaPoP!on theY-axis, for data sets having P/Poin the range of 0.05 to 0.3
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