ASTM D5349-1995(2006) Standard Test Method for Determination of the Moisture and Volatile Content of Sulfonated and Sulfated Oils by Hot-Plate Method《用热板法测量碘化油和硫酸盐油中含水量和挥发量的标准试验方法》.pdf

《ASTM D5349-1995(2006) Standard Test Method for Determination of the Moisture and Volatile Content of Sulfonated and Sulfated Oils by Hot-Plate Method《用热板法测量碘化油和硫酸盐油中含水量和挥发量的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D5349-1995(2006) Standard Test Method for Determination of the Moisture and Volatile Content of Sulfonated and Sulfated Oils by Hot-Plate Method《用热板法测量碘化油和硫酸盐油中含水量和挥发量的标准试验方法》.pdf（2页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 5349 95 (Reapproved 2006)Standard Test Method forDetermination of the Moisture and Volatile Content ofSulfonated and Sulfated Oils by Hot-Plate Method1This standard is issued under the fixed designation D 5349; the number immediately following the designation indicates the year oforig

2、inal adoption or, 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 per-centage o

3、f water and other compounds volatile at about 100Cexisting in a sample of sulfonated or sulfated oil, or both, byrapid evaporation. This test method is applicable only tosulfonated and sulfated oils that do not contain the following:mineral acids, free sulfonic acids or free sulfuric acid esters,amm

4、onia, acetic acid or similar volatile acids, alkali hydrox-ides, carbonates, acetates or similar salts that may react witholeic acid at elevated temperatures liberating volatile acids, orglycerin, diethylene glycol, xylene, or other compounds ofsimilar volatility. This test method was derived from T

5、estMethods D 500, Sections 10 through 14.1.2 The values stated in SI units are to be regarded as thestandard.1.3 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

6、 and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D 500 Test Methods of Chemical Analysis of Sulfonatedand Sulfated Oils3. Significance and Use3.1 This test method is intended to determine the moistureand volatile

7、 content of fats, oils, and fatliquors used in thesoftening and stuffing of leather.4. Apparatus4.1 The apparatus required consists of a glass-stopperedweighing flask, a glass beaker, and a suitable thermometer.4.1.1 Weighing Flasks, any suitable glass-stoppered weigh-ing flask of 10 to 15-mL capaci

8、ty.4.1.2 Beaker, Griffin low-form glass beaker with an ap-proximate capacity of 150 mL and a diameter of about 5 cm.4.1.3 Heat SourceThe source of heat may be either anelectric hot plate with or without asbestos paper or board cover,or an open flame under a suitable asbestos board and a wiregauze (t

9、o spread the heat).4.1.4 Thermometer, graduated from 90 to 150C, about 3 in.in length, and substantially constructed.5. Reagents5.1 Desiccating AgentAny suitable desiccating agent maybe used.NOTE 1Recent investigations seem to indicate that calcium chlorideis unreliable as a laboratory desiccating a

10、gent.5.2 Oleic Acid.6. Procedure6.1 Weigh approximately5gofoleic acid into the beakerand insert the thermometer. Heat the oleic acid gradually, whilestirring with the thermometer, until the temperature reaches130C. Place the beaker in an oven at 105 to 100C for 15 min,cool in a desiccator, and weigh

11、. Repeat the heating over the hotplate and in the oven until two successive weighings differ byless than 1.5 mg.6.2 Place about 6 g of the sample in the weighing flask anddetermine the weight accurately. Transfer the sample to thebeaker (containing the oleic acid and the thermometer) andweigh the fl

12、ask again. Heat the mixture exactly as in the taringof the beaker as described in 6.1. The loss in weight isequivalent to the moisture in the sample.7. Calculation7.1 Calculate the percentage of moisture and volatile matterin the sample as follows:Moisture and volatile matter, % 5 A/B! 3 100 (1)wher

13、e:A = loss of weight, g, andB = weight of sample, g.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 4119

14、57).Current edition approved April 1 2006. Published April 2006. Originallyapproved in 1993. Last previous edition approved in 2001 as D 5349 95(2001).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStan

15、dards volume information, 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.8. Precision and Bias8.1 Although this test method is widely used, precision andbias informatio

16、n is not available at this time.9. Keywords9.1 hot plate method; leather; moisture content; sulfonatedand sulfated oils; volatile contentASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this sta

17、ndard 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 responsible technical committee and must be reviewed every five years an

18、dif 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 consideration at a meeting of theresponsible technical committee,

19、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, 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 5349 95 (2006)2