ASTM D5627-1994(2009) 346 Standard Test Method for Water Extractable Residue from Particulate Ion-Exchange Resins《颗粒状离子交换树脂的水可萃取残留物的标准试验方法》.pdf

《ASTM D5627-1994(2009) 346 Standard Test Method for Water Extractable Residue from Particulate Ion-Exchange Resins《颗粒状离子交换树脂的水可萃取残留物的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D5627-1994(2009) 346 Standard Test Method for Water Extractable Residue from Particulate Ion-Exchange Resins《颗粒状离子交换树脂的水可萃取残留物的标准试验方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 5627 94 (Reapproved 2009)Standard Test Method forWater Extractable Residue from Particulate Ion-ExchangeResins1This standard is issued under the fixed designation D 5627; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revisio

2、n, 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 measurement of watersoluble extractable residue from particulate ion-exchan

3、ge res-ins based on elevated temperature extraction and gravimetricdetermination of residue.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, ass

4、ociated 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:2D 1129 Terminology Relating to WaterD 1193 Specification

5、 for Reagent WaterD 2187 Test Methods for Physical and Chemical Propertiesof Particulate Ion-Exchange ResinsD 2687 Practices for Sampling Particulate Ion-ExchangeMaterialsD 2777 Practice for Determination of Precision and Bias ofApplicable Test Methods of Committee D19 on Water3. Terminology3.1 Defi

6、nitions:3.1.1 For definitions of terms used in this test method, referto Terminology D 1129.4. Summary of Test Method4.1 A sample of particulate ion exchange material is con-tacted with water at an elevated temperature. After a specifiedcontact time, the concentration of soluble material in theaqueo

7、us phase is measured gravimetrically after filtration.5. Significance and Use5.1 The presence of water extractables in ion-exchangeresins can cause fouling of other materials downstream andcontamination of process water. The quantity of water extract-ables is sometimes used as a specification to ind

8、icate resinquality, and typical values are 0.01 to 0.1 %.5.2 It is recognized that this test method may not remove allpotential sloughage products and does not measure volatilecompounds. More extensive extraction and identification ofcompounds may be needed in specific cases.6. Interferences6.1 The

9、hygroscopic nature of some extracted compoundscan make it difficult to obtain a constant weight. Otherextraction times and temperatures may give results that are notcomparable to these.7. Apparatus7.1 Funnel, 60 mL with coarse frit.7.2 Filtration assembly.7.3 Glass fiber filters, without binder, pre

10、-rinsed with wa-ter.37.4 Weighing vesselPlatinum, nickel, or aluminum maybe used so long as there is no attack by the sample and constantweight can be achieved.7.5 Water bath, for use at 60 6 1C.8. Reagents8.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indi

11、cated, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,1This test method is under the jurisdiction of ASTM Committee D19 on Waterand is the direct responsibility of Subcommittee D19.08 on Membranes and IonE

12、xchange Materials.Current edition approved May 1, 2009. Published June 2009. Originallyapproved in 1994. Last previous edition approved in 2004 as D 5627 94 (2004).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Boo

13、k of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Gelman Type A/E, Millipore Type AP40, Whatman GF/C, or equivalent, havebeen found suitable for this purpose.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA

14、 19428-2959, United States.where such specifications are available.4Other grades may beused, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.8.2 Purity of WaterUnless otherwise indicated, referencest

15、o water shall be understood to mean reagent water conformingto Specification D 1193, Type I or lI.9. Sampling9.1 Collect the sample in accordance with Practices D 2687.In-service resins are taken after regeneration and rinse.10. Procedure10.1 Drain the sample, if necessary, with the drainingapparatu

16、s described in the draining apparatus section of TestMethods D 2187 to remove free water. Do not wash.10.2 Weigh (to the nearest 0.1 g) two 50-g portions of thedrained sample into clean, dry, 250-mL Erlenmeyer flasks(with stoppers) or BOD bottles. Also weigh (to the nearest 5mg) a 5-g portion of the

17、 drained sample for percent waterretention capacity according to Test Methods D 2187, TestMethod B.10.3 Transfer 200 mL of water by graduate to each of thetwo flasks containing sample. (Alternatively, measure the 200mL of water by weight into each flask.) Prepare another flaskand add 200 mL of water

18、 to serve as a blank. Stopper the flasksand maintain them at 60 6 1C for 18 6 2 h using a waterbath.10.4 Dry three weighing vessels to constant weight (61 mg)at 104 6 2C, cool in a desiccator and weigh to the nearest 0.1mg. (Platinum is preferred, but nickel or aluminum may beused.)10.5 Filter the e

19、ntire volume of each extract using either acoarse fritted funnel or filter assembly with glass fiber filter.Withdraw a 100-mL aliquot and transfer to a tared weighingvessel. (The remainder of the filtered extracts can be tested fortotal organic carbon or other parameters as desired.)10.6 Evaporate t

20、he water and then dry the weighing vesselsto constant weight (61 mg) at 104 6 2C (which can be doneovernight). A hot plate can be used to evaporate nearly all thewater so long as a layer of water covers the bottom of thevessel. Final drying is to be done in an oven. Weigh to thenearest 0.1 mg.11. Ca

21、lculation11.1 Calculate the water extractable residue, in percent, foreach of the two sample portions as follows:Water Extractable Residue, % wet basis 5A 2 B! 3 200CWater Extractable Residue, % dry basis 5A 2 B! 3 200SC 3D100Dwhere:A = residue from sample, in g,B = residue from blank, in g,C = drai

22、ned sample used, in g, andD = percent solids, calculated as 100 % water retentioncapacity (from Test Methods D 2187, Method B).(These calculations assume a 100-mL aliquot out of 200 mLextract.)12. Report12.1 Report the percent water extractable residue as theaverage of the two values obtained, using

23、 the wet or dry,reporting basis or both, as required.13. Precision and Bias13.1 Single-operator precision was determined using a com-posite sample of aged but unused strong acid, gel-type cationresin with an average solids content of 48.6 % by weight. Thesample was analyzed in triplicate by six oper

24、ators in onelaboratory. The operators who participated represented a widerange of experience levels. Since other sources of variabilityshould be relatively small (such as from the analytical bal-ances), the multiple laboratory variability is expected to mimicthe single-operator precision and is not

25、separately determined.All determinations were made using disposable aluminumweighing dishes. The following results were obtained:x = 0.393 % by weight, wet basis,So= 0.019 % by weight, wet basis,x = 0.812 % by weight, dry basis, andSo= 0.039 % by weight, dry basiswhere x is the arithmetic mean of th

26、e 18 determinations andSois the single-operator precision calculated in accordancewith D 2777.13.2 Since known standards are not available, bias cannotbe determined.14. Keywords14.1 extractables; fouling; ion exchange; residue; sloughage4Reagent Chemicals, American Chemical Society Specifications ,

27、AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlisted by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmaceutical Convention, Inc.

28、 (USPC), Rockville,MD.D 5627 94 (2009)2ASTM 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 the

29、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 of

30、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 shouldma

31、ke 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 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).D 5627 94 (2009)3