1、 Designation:D 2117-82(Reapproved 1988)E1 Standard Test Method for Reprinted from the Annual Book ol ASTM Standan:ls.Copyright ASTM II not listed in the current combined index,will eppear in the next edition.Melting Point of Semicrystalline Polymers by the Hot Stage Microscopy Method1 This standard
2、is issued under the fixed designation D 21 I 7;the number immediately following the designation indicates the year of original adoption or,in the case of revision,the year of last revision.A number in parentheses indicates the year of last reapproval.A supmcript epsilon(E)indicates an editorial chan
3、ge since the last revision or reapproval.This ten method has been approved for use by agencies of the Department of Defense and for listing in the DoD Index of Specifications and Standards.u NoTE-The safety hazards caveat was added editorially to the Scope and Sections 3 through S were renumbered in
4、 March 1988.1.Scope I.I This test method covers the detennination of the melting point of semicrystalline polymers(Note 1).NOTE I-Another procedure for the melting point of nylon resins may be found in Specification D 789.1.2 This test method is applicable to semicrystalline polymers in granular or
5、sheet form,0.04 mm(1.6 mils)or less in thickness.The normal operating temperature range is 30 to 230C.A maximum operating temperature of 350C can be obtained with special equipment(see 7.2).1.3 The values stated in SI units are to be regarded as the standard.The values in parentheses are given for i
6、nforma-tion only.1.4 This standard may involve hazardous materials,oper-ations,and equipment.This standard does not purport to address all of the safety problems associated with its use.It is the responsibility of the user of this standard to establish appropriate safety and health practices and det
7、ermine the applicability of regulatory limitations prior to use.2.Referenced Documents 2.1 ASTM Standards:D 618 Methods of Conditioning Plastics and Electrical Insulating Materials for Testing2 D 789 Specification for Nylon Injection Molding and Extrusion Materials2 D 1898 Practice for Sampling of P
8、lastics3 E 77 Method for Verification and Calibration of Liquid-in-Glass Thermometers4 3.Terminology 3.1 semicrystalline polymers-those polymers capable of forming at least two-dimensional intermolecular order as prepared or as developed by suitable thermal treatments.The amount and degree of perfec
9、tion of the ordering or crystalli-zation depends on the spatial relationship of the atoms in the 1 This test method is under the jurisdiction of ASTM Committee 0.20 on Plastics and is the direct responsibility of Subcommittee 020.30 on Thermal Properties(Section 020.30.07).Current edition approved N
10、ov.26,1982.Published January 1983.Originally published as D 2117-62T.Last previous edition D 2117-64(1978).l Annual Book of ASTM Standards,Vol 08.01.3 Annual Book of ASTM Standards,Vol 08.02.Annual Book of ASTM Standards,Vol 14.01.molecules,as well as the thermal or other treatment.4.Summary of Test
11、 Method 4.1 This test method consists of heating the sample by a hot stage unit mounted under a microscope and viewing it between crossed polars.When the crystalline material melts,the characteristic double refraction from the crystalline aggregates disappears.The point at which the double refrac-ti
12、on or birefringence completely disappears is taken as the melting point of the polymer.The effect of exposure to heat or air,or both,on the melting point can be detected by the use of this test method.S.Significance and Use 5.l This test method is useful for determining the melting point of semicrys
13、talline polymers where a high degree of precision is desired(see Section 14).5.2 The test method is suitable for specification accept-ance,manufacturing control,development,or research.6.Interferences 6.1 An appreciable increase in particle size above that specified will result in a large melting ra
14、nge and obscure the sharp end point.The presence of anisotropic crystals,for example,some inorganic substances,will reduce the accu-racy of the melting point due to the persistence of their double refraction after the greater part of the sample has melted.6.2 In some cases heat and air or heat alone
15、 will cause changes in the melting point.Where it has been shown that there is an effect of heat and air on the melting point,provision is made in 12.3 for an inert gas blanket.In the case of heat alone below the melting point(solid state polymer-ization)or at the melting point(further polymerizatio
16、n or degradation),the effect of heat should be determined by remelting a sample that has already been run.If the two determinations check within 1 c,the procedure as outlined may be followed.If the material is affected by heat alone,below or at the melting point,the melting point of the material cannot be determined by this test method.7.Apparatus 7.1 Compound Microscope,with magnifications from SOX to 1 OOx and at least a 6-mm working distance.A cap.analyzer and disk polarizer to fit the micros
