ASTM D4781-2003(2013) Standard Test Method for Mechanically Tapped Packing Density of Fine Catalyst Particles and Catalyst Carrier Particles《催化剂细粒和催化剂载体粒子机械振动堆积密度的标准试验方法》.pdf

《ASTM D4781-2003(2013) Standard Test Method for Mechanically Tapped Packing Density of Fine Catalyst Particles and Catalyst Carrier Particles《催化剂细粒和催化剂载体粒子机械振动堆积密度的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4781-2003(2013) Standard Test Method for Mechanically Tapped Packing Density of Fine Catalyst Particles and Catalyst Carrier Particles《催化剂细粒和催化剂载体粒子机械振动堆积密度的标准试验方法》.pdf（2页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4781 03 (Reapproved 2013)Standard Test Method forMechanically Tapped Packing Density of Fine CatalystParticles and Catalyst Carrier Particles1This standard is issued under the fixed designation D4781; the number immediately following the designation indicates the year oforiginal adopti

2、on or, in the case of revision, the year of last 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 me-chanically tapped pack

3、ing density of fine catalyst and catalystcarrier particles smaller than 0.8 mm in diameter.1.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3 This standard does not purport to address all of thesafety concerns, if any assoc

4、iated 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 Documents2.1 ASTM Standards:2D3766 Terminology Relating to Catalysts and CatalysisE177

5、Practice for Use of the Terms Precision and Bias inASTM Test MethodsE456 Terminology Relating to Quality and StatisticsE691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test Method3. Terminology3.1 DefinitionsSee Terminology D3766.4. Summary of Test Method4.1 A pre

6、conditioned sample of dried fine catalyst or cata-lyst carrier particles is tapped in a graduated cylinder. Themechanically tapped packing density is determined from theknown mass and tapped volume.5. Significance and Use5.1 This test method is for measuring the mechanicallytapped packing density of

7、 powders that are smaller than 0.8mm in diameter, such as Fluidized Catalytic Cracking Catalysts(FCC).6. Apparatus6.1 Graduated Cylinder, capacity 100 mL.6.2 Holder, acylinder holder weighing 454 g.6.3 Tapping Device, consisting of a baseplate with wormdrive, with specifications of 250 r/min camshaf

8、t speed, tappingstroke travel of 3.2 mm.6.4 Counter, a four-digit adjustable counter, which can bepreset to deliver number of taps between 1 and 9999.6.5 Desiccator, with a desiccant grade molecular sieve suchas 4A.6.6 Balance, having a sensitivity of 0.1 g.6.7 Drying Oven.7. Procedure7.1 Heat an ad

9、equate sample at 400 6 15C for not less than3 h. Normally, this treatment can take place in air. However, inthe case of materials that might react with air at elevatedtemperature (such as prereduced catalysts) the heat treatmentshould take place in an inert atmosphere. After heating, coolthe test sa

10、mple in a desiccator or other suitable container toeliminate the possibility of moisture adsorption prior to testing.NOTE 1These conditions may not be appropriate for all materials.NOTE 2Since many catalyst formulations are strong adsorbents, theuse of 4A indicating (cobalt-treated) molecular sieves

11、 as a desiccatingmedium is recommended. The desiccant should be regenerated at 220 to260C, as required.NOTE 3Multiple samples can be pretreated but must be desiccatedprior to analysis.7.2 Carefully pour between 90 and 100 mL of the testspecimen into the tared-graduated cylinder using a funnel. Toens

12、ure proper level, rotate the funnel while pouring the testspecimen. Weigh immediately to the nearest tenth of a gram.The entire transfer time should be between 35 and 50 s.7.3 Preset the counter to 1000 taps.1This test method is under the jurisdiction of ASTM Committee D32 onCatalysts and is the dir

13、ect responsibility of Subcommittee D32.02 on Physical-Mechanical Properties.Current edition approved March 1, 2013. Published March 2013. Originallyapproved in 1988. Last previous edition approved in 2008 as D478103(2008).DOI: 10.1520/D4781-03R13.2For referenced ASTM standards, visit the ASTM websit

14、e, 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.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1

15、7.4 Start the tapping device.7.5 When tapping is completed, read the tapped volume, V,to the nearest 1 mL by estimating the average level of thecatalyst surface in the cylinder.8. Calculation8.1 Calculate the mechanically tapped packing density asfollows:MTD 5 W/V (1)where:MTD = mechanically tapped

16、packing density, g/mL,W = mass of catalyst particles, g, andV = volume occupied by particles in measuring cylinder,mL.9. Precision and Bias39.1 Test ProgramAn interlaboratory study was conductedin which the named property was measured in two separate testmaterials in four separate laboratories. Prac

17、tice E691, modifiedfor non-uniform data sets, was followed for the data reduction.Analysis details are in the research report.9.2 PrecisionPairs of test results obtained by a proceduresimilar to that described in the study are expected to differ inabsolute value by less than 2.772 S, where 2.772 S i

18、s the 95 %probability interval limit on the difference between two testresults, and S is the appropriate estimate of standard deviation.Definitions and usage are given in Terminology E456 andPractice E177, respectively.Test Result(ConsensusMean), g/mL95 % Repeatability Interval(Within Laboratory) g/

19、mL(mean %)95 % Reproducibility Interval(Between Laboratories) g/mL(mean %)0.61950.93550.005 g/mL (0.87)0.010 g/mL (1.07)0.060 (9.74)0.041 (4.41)9.3 BiasThe procedure in this test method has no biasbecause the value of packing density can be defined only interms of the test method.10. Keywords10.1 ca

20、talyst; catalyst carrier; packing densityASTM 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 th

21、e riskof infringement 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 o

22、f this standard 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 should

23、make your views 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 obtaine

24、d 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). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).3Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Report RR:D32-1026.D4781 03 (2013)2