ASTM D5440-17 Standard Test Method for Determining the Melting Point of Fats and Oils.pdf

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1、Designation: D5440 17Standard Test Method forDetermining the Melting Point of Fats and Oils1This standard is issued under the fixed designation D5440; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A num

2、ber 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 is intended to determine the meltingpoint of all normal animal and vegetable fats and oils. This testmethod was derived f

3、rom ALCA H-16.1.2 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 user of this standard to

4、establish appro-priate safety, health, and environmental practices and deter-mine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accor-dance with internationally recognized principles on standard-ization established in the Decision on Princi

5、ples for theDevelopment of International Standards, Guides and Recom-mendations issued by the World Trade Organization TechnicalBarriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:E2251 Specification for Liquid-in-Glass ASTM Thermom-eters with Low-Hazard Precision Liquids2.2

6、American Leather Chemists Association Standard:ALCA H-16 Melting Point23. Significance and Use3.1 This test method is intended to determine the meltingpoint of all normal animal and vegetable fats.3.2 The natural fats and oils, that is, those of animal andvegetable origin, are mixtures of glycerides

7、 and other sub-stances and consist of a number of components. They do notexhibit either a definite or sharp melting point. Fats passthrough a stage of gradual softening before they becomecompletely liquid. The melting point then shall be defined bythe specific conditions of the method by which it is

8、 determinedand, in this case, it shall be the temperature at which the samplebecomes perfectly clear and liquid.4. Apparatus4.1 Melting Point Tubes, capillary globe tubing, with aninside diameter of 1 mm and an outside diameter of 2 mm,max. A convenient length is 50 to 80 mm.4.2 Thermometer, 2 to 68

9、C with 0.2C divisions (S12Cor S15C) and conforming to the requirements prescribed inSpecification E2251 for thermometers.4.3 Glass Beaker, 600 mL.4.4 Heat Source, gas burner or electric hot plate.5. Procedure5.1 The sample shall be melted and filtered through filterpaper to remove any impurities and

10、 the last traces of moisture.The sample shall be absolutely dry. At least three cleancapillary tubes shall be dipped in the completely liquid sampleso that the fat stands approximately 10 mm high in each tube.One end of the tube (where the sample is located) shall befused in a small flame, taking ca

11、re not to burn the fat.5.2 The tubes shall be placed in a beaker and held in arefrigerator at 4 to 10C overnight (16 h).5.2.1 The samples shall be completely liquid when the tubesare placed in the refrigerator. It is good practice to pass theends of the tubes containing the sample momentarily throug

12、hthe flame, just before they are taken to the refrigerator.5.3 After removing the tubes from the refrigerator, theyshall be attached to the thermometer, using a rubber band orany suitable means, so that the lower ends of the melting pointtubes shall be even with the bottom of the mercury bulb of the

13、thermometer. The thermometer shall be suspended in a 600 mLbeaker, which is about half full of clear distilled water and thebottom of the thermometer immersed approximately 30 mm.5.4 The starting bath temperature shall be adjusted to 8 to10C below the melting point of the sample at the beginning oft

14、he test. Agitation of the water bath shall be made with a smallstream of air or other suitable means, and heat shall be appliedso the batch temperature is increased at the rate of approxi-mately 0.5C per min.1This test method is under the jurisdiction of ASTM Committee D31 on Leatherand is the direc

15、t responsibility of Subcommittee D31.08 on Fats and OilsCurrent edition approved Sept. 1, 2017. Published October 2017. Originallyapproved in 1993. Last previous edition approved in 2009 as D5440 93 (2009).DOI: 10.1520/D5440-17.2Available from American Leather Chemists Assn., Texas Tech University,

16、P.O.Box 45300, Lubbock, TX 79409.Copyright 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 principles on standardization established in the Decision on Princ

17、iples for theDevelopment of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.15.5 Fats usually pass through an opalescent stage beforemelting completely. The heating shall be continued until thetubes are completely

18、 clear throughout. The temperature shallbe observed at which each tube becomes clear.5.6 The average of the melting point of all the tubes shall betaken and this average shall be reported as the melting point.6. Report6.1 Report the temperature recorded in 5.6 as the meltingpoint in this test method

19、.7. Precision and Bias7.1 This test method is adopted from the procedure of theAmerican Leather ChemistsAssociation where it has long beenin use, and where it was approved for publication before theinclusion of precision and bias statements was mandated. Theoriginal interlaboratory test data is no l

20、onger available. Theuser is cautioned to verify by the use of reference materials, ifavailable, that the precision and bias (or reproducibility) of thistest method is adequate for the contemplated use.8. Keywords8.1 fats and oils; leather; melting pointASTM International takes no position respecting

21、 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 riskof infringement of such rights, are entirely their own responsibility.This standar

22、d 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 this standard or for additional standardsand should be addressed to ASTM International

23、 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 your views known to the ASTM Committee on Standards, at the address shown below.Thi

24、s 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). 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:/ 172