ASTM C371-2009(2018) Standard Test Method for Wire-Cloth Sieve Analysis of Nonplastic Ceramic Powders.pdf

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1、Designation: C371 09 (Reapproved 2018)Standard Test Method forWire-Cloth Sieve Analysis of Nonplastic Ceramic Powders1This standard is issued under the fixed designation C371; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the yea

2、r 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. Scope*1.1 This test method covers the determination of the particlesize distribution of nonplastic ceramic powders such as

3、alumina, silica, feldspar, pyrophyllite, nepheline syenite, talc,titanates, and zircon using wire cloth sieves.1.2 Materials containing a large amount of fines, containingagglomerates, or that are nonfree-flowing, are wet-sieved toremove excessive fines or to disperse agglomerates beforeperforming t

4、he test. This technique is not applicable to mate-rials that are, to any degree, water soluble.1.3 The values stated in SI units are to be regarded asstandard. The values given in parentheses are mathematicalconversions to inch-pound units, or are other customary units(in the case of sieve frame dia

5、meter and sieve number), that areprovided for information only and are not considered standard.1.4 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, health, and

6、environmental practices and deter-mine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accor-dance with internationally recognized principles on standard-ization established in the Decision on Principles for theDevelopment of International St

7、andards, Guides and Recom-mendations issued by the World Trade Organization TechnicalBarriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:2C322 Practice for Sampling Ceramic Whiteware ClaysE11 Specification for Woven Wire Test Sieve Cloth and TestSieves3. Significance and Use3

8、.1 Sieve analyses are carried out to determine the particlesize distribution of powders which, in turn, are used to qualifythose materials as to their usefulness in the process underconsideration. Since particle size analyses have only relativesignificance, the results should be considered only wher

9、e theycorrelate with process characteristics. The parameter that isbeing measured in this test is the amount of material that willpass through a cloth having theoretically square openings. Itmust be remembered that all the holes are not square, noruniform in size, and the question of whether a given

10、 particlewill go through is a statistical one. Since each particle sizeanalysis method measures a unique physical parameter, theresults from one method may not agree with those fromanother. Particle size distributions play a role in such propertiesas bulk density, dustiness, and handling characteris

11、tics. Careshould be taken, however, when interpretations are made fromone or two points (sieves) on the distribution curve.4. Apparatus4.1 Balance, having a sensitivity of 0.05 g.4.2 Sieves, clean, unblinded, 205 mm (8 in.) in diameter,and conforming to Specification E11. At all times they shall bec

12、ertified by, or shall be calibrated with sieves certified by, theNational Institute of Standards and Technology. For wet-sieving, use full-height 50-mm (2-in.) sieves; these sieves andpan may be used for dry-sieving also. Half-height 25-mm(1-in.) sieves and pan shall be used for dry-sieving only. Th

13、esieves to be used may range from 45 m (No. 325) through 212m (No. 70).4.3 Drying Pans, about 205 mm (8 in.) in diameter and 25or 50 mm (1 or 2 in.) high.4.4 DryerFor drying, the use of an oven maintainedautomatically at 100 to 110C is recommended.4.5 Mechanical Shaking DeviceThe shaking device shal

14、lbe such as to produce a lateral and vertical motion of the sieve,accompanied by a jarring action so as to keep the samplemoving continuously over the surface of the sieve.4.6 In wet-sieving, the water should be slightly above roomtemperature (for example, a hot-cold mixer tap) and should besupplied

15、 by means of a fixed or hand-held spray.1This method is under the jurisdiction of ASTM Committee C21 on CeramicWhitewares and Related Productsand is the direct responsibility of SubcommitteeC21.04 on Raw Materials.Current edition approved Oct. 1, 2018. Published October 2018. Originallyapproved in 1

16、955. Last previous edition approved in 2014 as C371 09 (2014).DOI: 10.1520/C0371-09R18.2For 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 Summar

17、y page onthe ASTM website.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United StatesThis international standard was developed in accordance with internationally recognized principl

18、es on standardization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.15. Sampling5.1 Unit for SamplingEach carload shall be considered aunit for sam

19、pling.5.2 Gross Sample (See Practice C322)In collecting thegross sample from a carload shipped in bags, select a numberof bags equivalent to not less than 1 % of the total number ofbags in the car. Bags taken for sampling shall be from locationsevenly distributed, horizontally and vertically, throug

20、hout thecar. The gross sample shall consist of equal increments of notless than 227 g (0.5 lbs) from each of the bags taken forsampling. In collecting the gross sample from a carloadshipped in bulk, take equal increments of not less than 227 geach from points well distributed both horizontally and v

21、erti-cally.5.3 Test SampleObtain the test sample, of not less than110 g, by mixing the gross sample and then riffling or handquartering. Dry the entire test sample in an oven at 100 to110C to constant weight. Take a 100-g (Note 1) specimenweighed to the nearest 0.1 g shall be taken for sieve analysi

22、s.NOTE 1Alternatively, if less than 50 % passes the finest sieve, use a50-g specimen.6. Procedure6.1 Transfer the 100-g specimen to glazed paper and pro-ceed to 6.5, except as noted in 6.2.6.2 Alumina, talc, pyrophillite, other nonfree-flowingmaterials, and those materials containing agglomerates re

23、quirea preliminary wet sieving. Place the 100-g specimen into aglass beaker. Add 200 g of distilled water together with asuitable dispersion agent (Note 2) and stir the suspension witha rod until complete dispersion is obtained (Note 3). Pour thesuspension onto the finest sieve to be used. Wash any

24、residuein the beaker onto the sieve with a wash bottle.NOTE 2One suitable dispersion agent is 0.1 % sodium pyrophosphate.A 0.1 % sodium hexametaphosphate should be used for alumina.NOTE 3Dispersion aids, such as ultrasonic vibration and high shearmixers (food blenders) may be necessary to eliminate

25、agglomerates. Caremust be taken that undesirable grinding does not take place.6.3 While agitating, thoroughly wash the sieve under thesprayer head, the flow being sufficiently gentle to avoidsplashing. Sieving is complete when no more material passes.Determine this by catching the washings and exami

26、ning for thesolids.6.4 When sieving is complete, pass a sponge over theunderside of the sieve-cloth to draw out as much of the wateras possible. Rinse the retained solids with acetone, to speed updrying, and dry off any excess with a sponge. Do thisthoroughly to avoid dangerous levels of acetone in

27、the oven.Dry the sieve and specimen thoroughly at 100 to 110C andthen brush onto glazed paper.6.5 Assemble all the sieves to be used in the test with thecoarsest sieve on top and the others under it in order ofdecreasing sieve opening size. Transfer the specimen from theglazed paper to the top or co

28、arsest sieve and shake the entireseries of sieves. It is recommended that this agitation be donemechanically. For hand-sieving, hold the nest of sieves, withpan and cover attached, in one hand and gently strike the sideabout 150 times/min against the palm of the other hand. Theside of sieves next to

29、 the striking hand should be slightly higherthan the other side so that sample will be well distributed oversieves. Turn the sieve-nest every 25 strokes about one sixth ofa revolution in the same direction. With either mechanical orhand agitation, the agitation should continue to the point wherenot

30、more than 0.05 g passes a given sieve in 1 min.6.6 Separate the nested sieves and carefully remove theresidue from each and weigh to the nearest 0.1 g. Theseweights in grams will equal the percent of residue on eachsieve (if a 100-g specimen was used).7. Calculation and Report7.1 Calculate and repor

31、t the cumulative percent passing, orthe residue on each sieve, as required, to the nearest wholepercent.8. Precision and Bias8.1 PrecisionThe precision of the procedure in TestMethod C371 for measuring particle size is being determined.8.2 BiasThe true value of the particle size can only bedefined i

32、n terms of a test method. Within this limitation, thismethod has no known bias.9. Keywords9.1 alumina; particle size distribution; sieve analysis; silica;wet-sievingC371 09 (2018)2SUMMARY OF CHANGESCommittee C21 has identified the location of selected changes to this standard since the last issue(C3

33、71 89 (2003) that may impact the use of this standard. (Approved Jan. 1, 2009.)(1) Addition of 1.3 describing the use of units in this testmethod, with renumbering of the subsequent sections of theScope.ASTM International takes no position respecting the validity of any patent rights asserted in con

34、nection 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 respon

35、sible 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

36、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 views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 1

37、00 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:/ 09 (2018)3

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