ASTM D5352-1995(2006) Standard Test Method for Determination of Organically Combined Sulfuric Anhydride Ash-Gravimetric Test Method C《用灰分重量测试法C测量有机合成三氧化硫的标准试验方法》.pdf

1、Designation: D 5352 95 (Reapproved 2006)Standard Test Method forDetermination of Organically Combined Sulfuric AnhydrideAsh-Gravimetric, Test Method C1This standard is issued under the fixed designation D 5352; the number immediately following the designation indicates the year oforiginal adoption o

2、r, in the case of revision, the year of 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 organi-cally combined sulfur

3、ic anhydride existing in a sample ofsulfonated or sulfated oil, or both, by extracting the undecom-posed sulfonated or sulfated fat and other fatty matter over anacidulated, concentrated salt solution, and ashing the purifiedextract. This test method is applicable to all types of sulfonatedand sulfa

4、ted oils, including true sulfonic acid oils and thosecontaining sodium acetate or similar partially titratable com-pounds. This test method was derived from Test MethodsD 500, Sections 25 through 28.1.2 The values stated in SI units are to be regarded as thestandard.1.3 This standard does not purpor

5、t 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.2. Referenced Documents2.1 ASTM Standards:2D 500

6、 Test Methods of Chemical Analysis of Sulfonatedand Sulfated Oils3. Significance and Use3.1 This test method is intended for the determination oforganically combined sulfuric anhydride in sulfonated andsulfated fats and oils.4. Reagents4.1 Ethyl Ether.4.2 Hydrogen Peroxide (30 %)Concentrated hydroge

7、nperoxide (H2O2).4.3 Methyl Orange Indicator Solution (1 g/L)Dissolve 0.1g of methyl orange in 100 mL of water.4.4 Sodium Chloride (NaCl), solid.4.5 Sodium Sulfate (Na2SO4), anhydrous.5. Procedure5.1 The procedure consists of isolating and purifying thefatty matter as it exists in the original oil b

8、y dissolving thesample in a solvent, acidifying and washing with saturatedbrine, and ashing the purified extract. If the sample containsammonia, the ammonia shall first be expelled before thedetermination is made on the sample.5.1.1 In the Absence of AmmoniaProceed as described inthe separation of p

9、urified oil (6.1.1 Method B), combining theether layers in the first funnel rather than in the decompositionflask. Carefully remove any water that may settle and dehy-drate the ether layer as follows: add5gofanhydrous Na2SO4,shake vigorously for 5 min, and filter directly into a 150-mLbeaker placed

10、in a bath of warm water. Wash the flask and filterwith ether until free from fat (absence of oil stains on the filterpaper after drying) and add the filtrate to the beaker. To avoidcreeping of the oil, the volume in the beaker should at no timeduring the filtering and washing exceed 50 mL (one third

11、 full).Evaporate the ether solution until the volume has been reducedto about 20 mL and transfer the residue to a tared 50-mLcrucible (high form). Immerse the crucible in a 100-mL beakercontaining warm water until practically all of the ether hasevaporated. Rinse the beaker with two 10-mL and three

12、5-mLportions of ether, or until all of the oil has been transferred tothe crucible; allow each portion of rinsing ether to evaporatebefore the next rinsing is made. Burn gently the solvent-freeresidue, and finally ignite at a dull red heat to constant weight.To prevent creeping of the oil and to has

13、ten evaporation, stirthe solution with a glass rod; before the oil is burned, wipe therod clean with ashless filter paper and add the paper to thecrucible. To oxidize traces of carbon or sodium sulfide thatmight form, moisten the ash with H2O2and again carefullyignite to constant weight. Calculate t

14、he percentage of ash asfollows:1This test method is under the jurisdiction of ASTM Committee D31 on Leatherand is the direct responsibility of Subcommittee D31.08 on Fats and Oils.This testmethod was developed in cooperation with the American Leather Chemists Assn.(Method H 44-1957).Current edition

15、approved April 1, 2006. Published April 2006. Originallyapproved in 1993. Last previous edition approved in 2001 as D 5352 95(2001).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume inform

16、ation, refer to the standards Document Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.Extracted ash, % 5 A/B! 3 100 (1)where:A = weight of ash, g, andB = weight of sample, g.5.1.2 In the Presence of A

17、mmoniaDissolve 5 to8gofthesample in 80 mL of water in a 300-mL beaker. Add 10 mL of1 N NaOH solution and boil the solution gently until wet litmuspaper no longer indicates ammonia. Cool the solution, transferto a 300-mL separatory funnel, and add about 35 g of solidNaCl or enough to make the final s

18、olution a 25 % NaClsolution. Add five drops of methyl orange solution and com-plete the neutralization, extraction, etc., in accordance with theprocedure described in 5.1.1.6. Calculation6.1 Calculate the percentage of organically combined sul-furic anhydride as follows:Organically combined sulfuric

19、 anhydride, % 5 1.1267 A (2)where:A = extracted ash, %, and1.1267 = molecular ratio of 2SO3:Na2SO4.7. Precision and Bias7.1 Although this test method is widely used, precision andbias information is not available at this time.8. Keywords8.1 ash-gravimetric; leather; sulfated fats and oils; sul-fonat

20、ed fats and oils; sulfuric anhydrideASTM 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 ris

21、kof 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 thi

22、s 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 shouldmake

23、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 5352 95 (2006)2