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本文(ASTM D5349-1995(2012) Standard Test Method for Determination of the Moisture and Volatile Content of Sulfonated and Sulfated Oils by Hot-Plate Method 《用热板法测定磺化油和硫酸化油中水分量和挥发物含量的标准试验.pdf)为本站会员(registerpick115)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM D5349-1995(2012) Standard Test Method for Determination of the Moisture and Volatile Content of Sulfonated and Sulfated Oils by Hot-Plate Method 《用热板法测定磺化油和硫酸化油中水分量和挥发物含量的标准试验.pdf

1、Designation: D5349 95 (Reapproved 2012)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 D5349; the number immediately following the designation indicates the year oforigin

2、al adoption or, in the case of revision, 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 determination of the per-centage of w

3、ater 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,ammoni

4、a, 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 Test

5、Methods D500, Sections 10 through 14.1.2 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, associated with its use. It is theresponsibility of the us

6、er 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:2D500 Test Methods of ChemicalAnalysis of Sulfonated andSulfated Oils3. Significance and Use3.1 This test method

7、 is intended to determine the moistureand volatile 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 gla

8、ss-stoppered weigh-ing flask of 10 to 15-mL capacity.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

9、under a suitable asbestos board and a wiregauze (to 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 c

10、hlorideis unreliable as a laboratory desiccating agent.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

11、to 100C for 15 min,cool in a desiccator, and weigh. 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 t

12、he oleic acid and the thermometer) andweigh the flask 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:Mo

13、isture and volatile matter, % 5 A/B! 3 100 (1)1This test method is under the jurisdiction of ASTM Committee D31 on Leatherand is the direct responsibility of Subcommittee D31.08 on Fats and OilsThis testmethod was developed in cooperation with the American Leather Chemists Assn.(Method H 411957).Cur

14、rent edition approved April 1, 2012. Published April 2012. Originallyapproved in 1993. Last previous edition approved in 2006 as D5349 95(2006).DOI: 10.1520/D5349-95R12.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annua

15、l Book of ASTMStandards 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.where:A = loss of weight, g, andB = weight of sample, g.8. Precision and Bias

16、8.1 Although this test method is widely used, precision andbias information 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 asserte

17、d 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 riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by th

18、e 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 this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive

19、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 your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM Internat

20、ional, 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). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).D5349 95 (2012)2

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