ASTM D4058-1996(2015) Standard Test Method for Attrition and Abrasion of Catalysts and Catalyst Carriers《催化剂和催化剂载体磨耗及磨损性的标准试验方法》.pdf

《ASTM D4058-1996(2015) Standard Test Method for Attrition and Abrasion of Catalysts and Catalyst Carriers《催化剂和催化剂载体磨耗及磨损性的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4058-1996(2015) Standard Test Method for Attrition and Abrasion of Catalysts and Catalyst Carriers《催化剂和催化剂载体磨耗及磨损性的标准试验方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4058 96 (Reapproved 2015)Standard Test Method forAttrition and Abrasion of Catalysts and Catalyst Carriers1This standard is issued under the fixed designation D4058; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the

2、 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 attri-tion and abrasion resistance of catalysts and catalyst

3、 carriers. Itis applicable to tablets, extrudate, spheres, and irregularlyshaped particles larger than about116 in. (1.6 mm) and smallerthan about34 in. (19 mm). The materials used in developingthe method exhibited losses on attrition less than 7 %;however, the method should be applicable to materia

4、ls givingmuch higher attritions.1.2 The values stated in inch-pound units are to be regardedas standard. The values given in parentheses are mathematicalconversions to SI units that are provided for information onlyand are not considered standard.1.3 This standard does not purport to address all of

5、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 Documents2.1 ASTM Standards:2E177 Practice for Use of

6、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. Summary of Test Method3.1 A sample of catalyst or catalyst carrier is rotated for afixed number of rev

7、olutions in a cylindrical drum having asingle baffle. Fines produced by attrition and abrasion in thetest are determined by sieving through a standard sieve.4. Significance and Use4.1 This test method is considered to be a measure of thepropensity of a catalyst to produce fines in the course oftrans

8、portation, handling, and use. However, there is no abso-lute level of acceptability. The values obtained are significantprincipally in relation to values for other materials (or othersamples of the same material) of comparable size.5. Apparatus5.1 Acylindrical drum with inside dimensions of 10 in. (

9、254mm) diameter and 6 in. (152 mm) long with a single radialbaffle 2 in. (51 mm) high extending the full length of thecylinder. A lid shall be provided and secured to the containerwithAllen-head screws, wing nuts or other suitable means as toensure that no fines escape during the test. The inside of

10、 thedrum should have a surface roughness no greater than about250 in. (6.4 m). (The roughness of cold-rolled steel or asmooth grind on a lathe is satisfactory.) A suitable design isshown in Fig. 1.5.2 Any convenient means of rotation, such as a ball millroller, geared to give the desired rate of rot

11、ation of the drum.6. Sampling6.1 Obtain a representative sample of about 110 g of thematerial to be tested by gently splitting or quartering. Anysampling technique requiring extensive agitation or handlingwill cause some attrition and, therefore, compromise the resultsof the test.6.2 Gently sieve th

12、e sample on a No. 20 (850-m) ASTMsieve.6.3 Transfer the presieved sample to a widemouthed con-tainer tared to the nearest 0.01 g.6.4 Dry the presieved sample in air for3hat400C. It maybe necessary to modify or eliminate this step when testingmaterials that might be decomposed or drastically altered

13、bythe drying conditions.NOTE 1For example, an activated carbon catalyst may be treated for4 h at 190C in a vacuum oven.6.5 Cool the dried sample for at least 30 min in a desiccatorusing freshly regenerated 4A molecular sieves as the desiccant.The molecular sieves shall be regenerated at 220 to 260C.

14、1This test method is under the jurisdiction of ASTM Committee D32 onCatalysts and is the direct responsibility of Subcommittee D32.02 on Physical-Mechanical Properties.Current edition approved Dec. 1, 2015. Published December 2015. Originallyapproved in 1981. Last previous edition approved in 2011 a

15、s D405896(2011). DOI:10.1520/D4058-96R15.2For 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.Copyright ASTM Inter

16、national, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1NOTE 2Multiple samples can be handled simultaneously in 6.4 and6.5. However, they should remain in a desiccator before analyzing.7. Procedure7.1 Clean the test cylinder and lid of the apparatus using afine-

17、bristle brush.7.2 Weigh about 100 g of the pretreated sample from 6.5 tothe nearest 0.01 g. Record this weight as A.7.3 Transfer the weighed sample into the test cylinder.7.4 Carefully seal the cover and position the test cylinder forrotation.7.5 Rotate the test cylinder 1800 revolutions at a rate o

18、f 606 5 rpm.7.6 After the rotation prescribed in 7.5, rotate the testcylinder until the baffle is at the top and tap the test cylinderwith a rubber mallet several times to allow the fines to settle tothe bottom of the test cylinder.7.7 Place a No. 20 (850-m) ASTM sieve with pan underthe test cylinde

19、r and carefully remove the cover.7.8 Pour the test sample onto the sieve. Use a fine-bristlebrush to clean out the test cylinder and its cover.7.9 Sieve the fines into the pan by gently shaking the sieveby hand; avoid excessive agitation (refer to 6.1).7.10 Dry the fraction on the sieve at the same

20、conditionsused for the original sample (refer to 6.4).7.11 Weigh the dried fraction to the nearest 0.01 g. Recordthis weight as B.8. Calculation8.1 Calculate the percent loss on attrition as follows:Loss on attrition, % 5A 2 BA3100 (1)Example: A = 100.00 g test sampleB = 98.60 g on sieve100.00 2 98.

21、60!100.003100 5 1.4% (2)When the loss on attrition is less than 1.0 %, report it as “lessthan 1 %.”9. Precision and Bias39.1 Test ProgramAn interlaboratory study was conductedin which the named property was measured in two separate testmaterials in nine separate laboratories. Practice E691, modified

22、for 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 2.772S, where 2.772S is the 95%probability

23、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.3Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Re

24、search Report RR:D32-1003.FIG. 1 Drum for Determining Attrition and Abrasion (Stainless Steel Fabrication)D4058 96 (2015)295 % Repeatability 95 % ReproducibilityTest Result Interval (Within Interval (Between(Consensus Laboratory) weight % Laboratories) weight %Mean) weight % (% of mean) (% of mean)6

25、.24 0.31 (4.9) 0.90 (14.5)3.35 0.35 (10.4) 0.91 (27.1)9.3 BiasThis test method is without known bias, sincethere is no known standard for comparison.10. Keywords10.1 attrition; abrasion; catalyst; finesASTM International takes no position respecting the validity of any patent rights asserted in conn

26、ection 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 infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the respons

27、ible 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 standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful c

28、onsideration 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 views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 10

29、0 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). Permission rights to photocopy the standard may also be secured from the Copyright Clearance Center, 222Rosewood Drive, Danvers, MA 01923, Tel: (978) 646-2600; http:/ 96 (2015)3