ASTM D4591-2007 Standard Test Method for Determining Temperatures and Heats of Transitions of Fluoropolymers by Differential Scanning Calorimetry《用差式扫描量热法测定含氟聚合物温度和转化热的标准试验方法》.pdf

《ASTM D4591-2007 Standard Test Method for Determining Temperatures and Heats of Transitions of Fluoropolymers by Differential Scanning Calorimetry《用差式扫描量热法测定含氟聚合物温度和转化热的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4591-2007 Standard Test Method for Determining Temperatures and Heats of Transitions of Fluoropolymers by Differential Scanning Calorimetry《用差式扫描量热法测定含氟聚合物温度和转化热的标准试验方法》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D 4591 07Standard Test Method forDetermining Temperatures and Heats of Transitions ofFluoropolymers by Differential Scanning Calorimetry1This standard is issued under the fixed designation D 4591; the number immediately following the designation indicates the year oforiginal adoption or

2、, 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.This standard has been approved for use by agencies of the Department of Defense.1. Scope*

3、1.1 This test method defines conditions for the use ofdifferential scanning calorimetry (DSC) with fluoropolymers.It covers the use of DSC analyses with the fluoropolymers,PTFE, PVDF, PCTFE, and PVF and their copolymers PFA,MFA, FEP, ECTFE, EFEP, VDF/HFP, VDF/TFE/HFP, VDF/CTFE. The test method is ap

4、plicable to the analysis of powdersas well as samples taken from semi-finished or finishedproducts. The nature of fluoropolymers is such that specialprocedures are needed for running DSC analysis and interpret-ing the results.1.2 The values stated in SI units as detailed in IEEE/ASTMSI10 are to be r

5、egarded as the standard.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 and health practices and determine the applica-bility of regulatory limitations prio

6、r to use.NOTE 1There is currently no ISO standard that duplicates this testmethod. ISO 12086-1 and ISO 12086-2 cover similar testing and refer-ence this test method for testing conditions.2. Referenced Documents2.1 ASTM Standards:2D 1600 Terminology for Abbreviated Terms Relating toPlasticsD 3418 Te

7、st Method for Transition Temperatures of Poly-mers By Differential Scanning CalorimetryD 4894 Specification for Polytetrafluoroethylene (PTFE)Granular Molding and Ram Extrusion MaterialsD 4895 Specification for Polytetrafluoroethylene (PTFE)Resin Produced From DispersionE 473 Terminology Relating to

8、 Thermal Analysis and Rhe-ologyE 793 Test Method for Enthalpies of Fusion and Crystalli-zation by Differential Scanning CalorimetryIEEE/ASTM SI10 Standard for Use of the InternationalSystem of Units (SI) (the Modern Metric System)2.2 ISO Standards:3ISO 12086-1 PlasticsFluoropolymer Dispersion andMol

9、ding and Extrusion MaterialsPart 1: Designationand SpecificationISO 12086-2 PlasticsFluoropolymer Dispersion andMolding and Extrusion MaterialsPart 2: Preparation ofTest Specimen and Determination of Properties3. Terminology3.1 Definitions:3.1.1 differential scanning calorimetry (DSC)a techniquein w

10、hich the difference in energy inputs into a substance and areference material is measured as a function of temperature,while the substance and reference material are subjected to acontrolled increase or decrease in temperature.3.1.2 Refer to Terminology E 473 for general terminologyused in this test

11、 method.3.2 Abbreviated Terms:3.2.1 Abbreviations used in this test method are in accor-dance with Terminology D 1600.3.2.2 PTFEpolytetrafluoroethylene.3.2.3 PFAperfluoro(alkoxy alkane) resin.3.2.4 FEPperfluoro(ethylene-propene) copolymer.3.2.5 ETFEethylene-tetrafluoroethylene copolymer.3.2.6 PVDFpo

12、ly(vinylidene fluoride).3.2.7 PCTFEpolymonochlorotrifluoroethylene.3.2.8 ECTFEethylene-monochlorotrifluoroethylene co-polymer.3.2.9 EFEPethylene-perfluoroethylene-propene copoly-mer.3.2.10 VDF/HFPvinylidene fluoride-hexafluoropropenecopolymer.1This test method is under the jurisdiction ofASTM Commit

13、tee D20 on Plasticsand is the direct responsibility of Subcommittee D20.15 on Thermoplastic Materi-als.Current edition approved March 1, 2007. Published March 2007. Originallyapproved in 1987. Last previous edition approved in 2001 as D 4591 - 01.2For referenced ASTM standards, visit the ASTM websit

14、e, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Available from American National Standards Institute (ANSI), 25 W. 43rd St.,4th Floor, New York, NY 10036.1*A Sum

15、mary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.3.2.11 VDF/TFEvinylidene fluoride-tetrafluoroethylenecopolymer.3.2.12 VDF/TFE/HFPvinylidene fluoride-tetrafluoroethylene-hexaf

16、luoropropene copolymer.3.2.13 VDF/CTFEvinylidene fluoride-chlorotrifluoroethylene copolymer.3.2.14 PVFpoly(vinyl fluoride).3.2.15 MFAperfluoromethylvinylether-tetrafluoroethylene copolymer.3.2.16 SSGstandard specific gravity.4. Significance and Use4.1 DSC analysis may be used with fluoropolymers toa

17、chieve at least four different objectives as follows:4.1.1 To measure transition temperatures to aid in theidentification of the various fluoropolymers, individually or inmixtures;4.1.2 To compare the relative levels of crystalline content oftwo or more specimens of a sample of a fluoropolymer relat

18、iveto another sample by measuring the heat of fusion;NOTE 2Absolute values of crystalline content cannot be determineduntil values for heats of fusion of the completely crystalline polymers areavailable.4.1.3 To characterize PTFE (DSC thermal curves deter-mined on powders or products of PTFE that ha

19、ve never beenmelted convey appreciable information about details of mor-phology and molecular structure);44.1.4 To supplement the test for standard specific gravity(SSG) described in Specifications D 4894 and D 4895 by usingthe heat of crystallization of pure PTFE homopolymer, depend-ing on the rela

20、tive molecular weight of the specimen. Thescopes of these specifications, however, include PTFE resinsmodified with small amounts of comonomers, and manycommercial PTFE resins are modified in this manner. Thesemodifications can have profound effects on crystallizationbehavior. Published relationship

21、s4between heat of crystalliza-tion and molecular weight refer to pure PTFE homopolymersand, therefore, cannot be applied to the modified resins.5. Apparatus5.1 Differential Scanning Calorimeter, capable of heatingand cooling rates of at least 10.0 C/min and of recordingautomatically the differential

22、 heat flow between a specimenand a reference material as a function of time, both to therequired sensitivity and precision. For comparison purposes,the same heating rate shall be used for all calibrations and testruns. Thermal curves are recorded using a computerized datacollection system or on a ti

23、me-based recorder. The resultingcurves are used for the measurement of peak areas either bycomputer integration or an alternative area measuring proce-dure. The instrument should have a sensitivity for heat flowsufficient to provide a precision of 61 % when run using asuitable standard for calibrati

24、on, such as indium. The instru-ment must have a precision of 61 % for either the computer-ized data collections or over a time-base range of 0.1 to 2.0min/cm of chart.NOTE 3Most DSC systems report data with a temperature ordinate.The temperature values are directly related to time based on the heati

25、ng orcooling rate. Integrated areas measured from the DSC curves will bedirectly proportional to the differential caloric input.NOTE 4Noncomputerized area measurement shall be done with aprecision of 61 % or better.5.2 Specimen Holders and Covers, made from aluminum orother materials of high thermal

26、 conductivity that do not reactwith the specimen. It is preferable to use holders designed forthe particular DSC instrument being used. For holders forwhich the cover has the shape of a small cup, the top should beinserted with the open side of the cup up.5.3 Nitrogen, or other inert gas supply for

27、purging purposes.5.4 Balance, with capacity greater than 15 mg, capable ofweighing to the nearest 0.01 mg.6. Procedure6.1 General RequirementsIn general, Test MethodD 3418 shall be used whenever possible. There are instances,however, when followingTest Method D 3418 will not give thedesired results,

28、 will not provide information needed for properinterpretation of the resultant thermal curve, or will requiremore time for the analysis than need be spent for results havingsuitable precision. Examples of these instances include thefollowing:6.1.1 The requirement that scans be started at room tem-pe

29、rature, a provision usually not required with all fluoropoly-mers;6.1.2 At times the thermal curve that results from theanalysis provides information that cannot be interpreted in auseful manner by Test Method D 3418, but can be interpretedfollowing the procedures of Section 7.6.2 CalibrationThe pro

30、cedures for calibration provided inTest Method E 793 shall be used. The comments in TestMethod D 3418 are helpful when reviewed. The calibration iscarried out by using an appropriate amount of at least twoselected standards weighed to the nearest 0.01 mg. Select thestandard materials so that their r

31、ange includes the first-ordertransition temperature(s) of the fluoropolymer being tested. Ithas been found that only one standard is needed to validate theinstrument between calibrations.6.3 A standard specimen mass shall be in the range of 9 to10 mg weighed to an accuracy of 0.01 mg. For routine an

32、alysis,a nonstandard specimen size may be used in cases whereequivalence to the standard mass has been established forparticular properties. A specimen mass different from thestandard shall be reported.NOTE 5Thermal curves from such analyses not using the standardspecimen mass range may not compare

33、with curves obtained using thestandard mass range. Due to the sensitivity of the peak, Tm, to thespecimen size, the results may be outside the expected precision and bias.6.4 Place the test specimen in the DSC sample pan, coverwith pan cover, and crimp. Place the pan with specimen in theDSC sample h

34、older or cell at the heating cycle startingtemperature.4Sperati, C. A., “Polytetrafluoroethylene: History of Its Development and SomeRecent Advances” (67 references), High Performance Polymers: Their Origin andDevelopment, Seymour and Kirshenbaume (eds), Marcel Deckker, NewYork, 1986,p. 274.D4591072

35、6.5 Heating and cooling rates of 10C/min shall be standard(except as noted in Table 1). Other heating rates may be usefulfor some routine analyses. Any rates different from the stan-dard must be reported and thermal curves from such analysesmust not be used in comparison with curves obtained using t

36、hestandard rate.NOTE 6Other heating rates will change the observed melting andcooling temperature values.6.6 Before starting the scan at the controlled rate, heat thespecimen at the highest rate possible with the instrument beingused to the temperature shown in Table 1 for the fluoropolymerbeing tes

37、ted. The time required to reach thermal equilibrium atthe starting temperature will depend on the particular instru-ment being used. If heats of crystallization are being deter-mined, stop the heating at the end temperature given in Table1. Use a dwell time long enough to remove (or normalize) anyho

38、mogenous crystal nucleation effects of the polymer beforestarting the cooling. For PVDF a dwell time of ten minutes at210C is required. DSC analysis used to determine the pres-ence of other components in the specimens should usually bestarted at room temperature.NOTE 7Residual homogeneous crystal nu

39、clei can affect the values ofTm, Tc, and heats of transition.7. Calculation7.1 Determining Transition TemperaturesAs illustrated inboth Fig. 1 and in Test Method D 3418, the temperature of amelting peak on a DSC thermal curve shall be designated Tm1,Tm2, etc., numbered in order of increasing tempera

40、ture. Thetemperature at which a tangent to the curve intercepts anextension of the base line on the low-temperature side shall bedesignated Tf, and the temperature at which a tangent to thecurve intercepts an extension of the base line on the high-temperature side shall be designated Te.NOTE 8Fluoro

41、polymers can have various crystal forms. Therefore,the resulting DSC curve can have two or more peaks or peaks withpronounced shoulders. The Tm1value of one sample with one peak maybe the same as the Tm2value of another sample with two peaks.7.1.1 Fig. 1 was selected to show two endothermic peaksdur

42、ing a melting cycle, and the peaks are identified on thefigure. Determination of the temperatures for crystallization iscarried out in a comparable manner, as shown both in Fig. 2and in Figure 1 of Test Method D 3418.7.2 Determining Heats of TransitionCalculation of heatsof fusion or crystallization

43、 shall be done in accordance withTest Method D 3418. Instrumental determination of heats oftransition requires temperature ranges to determine heat con-tent. Due to instrument start-up effects that can last up to 1 or2 min, the integration range should be 10 to 20C above thestarting and below the fi

44、nal temperature. A smaller integrationrange would be Tf 20 or 30C and Te+ 10 or 20C. Thecalculated heat value should not be sensitive to small changes(5C in the integration range).TABLE 1 Recommended Temperature Limits for DSCMeasurements and for Integrating DSC Thermal Curves withVarious Fluoropoly

45、mersA, BFluoropolymerHeating CurveDwellTime,minCooling CurveRate,C/minTypicalValues,CCStart,CEnd,CStart,CEnd,C(homopolymers)PTFEPCTFE270130380250 538025019527019513010100.2315360200225PVDF(copolymers)25 210 10 210 25 10 160175PFA 200 350 350 200 10 280330MFA 200 350 350 200 10 260290FEP 200 320 320

46、200 10 240290ETFE 140 320 320 140 10 210270ECTFE 200 300 300 200 10 230250VDF/HFP 25 210 10 210 25 10 130165VDF/CTFE 25 210 10 210 25 10 130165VDF/TFE 25 200 10 200 25 10 100150VDF/TFE/HFP 25 150 10 150 25 10 130AReport peaks (and shoulders) from lowest to highest (for example, Tm1 Tm2 Tm3. ).BThe i

47、ntegration range should be 10 to 20C above the starting and below thefinal temperature. A smaller integration range would be Tf 20 or 30C and Te+ 10 or 20C. The calculated heat value should not be sensitive to small changes(5C in the integration range).CTypical values cited represent an expected ran

48、ge of peak values for this test.These values shall not be used for specifications. Copolymer peak values (andintensities) will vary with comonomer ratios and may not be within the cited ranges.FIG. 1 Heating CurveFIG. 2 Cooling CurveD4591073NOTE 9Multiple crystal forms and the complicated morphology

49、 ofVDF based copolymers can make it difficult to determine heats oftransition on this polymer.7.3 Calculation of Results of Determinations made in ac-cordance with the objectives of 4.1 may include transitionpeaks or shoulders and transition heats. Additional determina-tions may use the steps listed in 7.3.1 and 7.3.2.7.3.1 The ratio of peak heights may be useful in character-izing materials that show two or more distinct peaks orshoulders. This ratio is determined by dividing the height of ahigher-temperature peak by the