ASTM D3531 D3531M-2011 Standard Test Method for Resin Flow of Carbon Fiber-Epoxy Prepreg《碳纤维环氧树脂预浸料树脂的流动性的标准试验方法》.pdf

《ASTM D3531 D3531M-2011 Standard Test Method for Resin Flow of Carbon Fiber-Epoxy Prepreg《碳纤维环氧树脂预浸料树脂的流动性的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D3531 D3531M-2011 Standard Test Method for Resin Flow of Carbon Fiber-Epoxy Prepreg《碳纤维环氧树脂预浸料树脂的流动性的标准试验方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D3531/D3531M 11Standard Test Method forResin Flow of Carbon Fiber-Epoxy Prepreg1This standard is issued under the fixed designation D3531/D3531M; the number immediately following the designation indicates theyear of original adoption or, in the case of revision, the year of last revisio

2、n. A number in parentheses indicates the year of lastreapproval. A superscript epsilon () 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. Scope1.1 This test method covers the determination of the

3、amountof resin flow that will take place from prepreg tape or sheetunder given conditions of temperature and pressure.1.2 The values stated in either SI units or inch-pound unitsare to be regarded separately as standard. The values stated ineach system may not be exact equivalents; therefore, eachsy

4、stem shall be used independently of the other. Combiningvalues from the two systems may result in non-conformancewith the standard.1.2.1 Within the text, inch-pound units are shown in brack-ets.1.3 This standard does not purport to address all of thesafety concerns, if any, associated with its use.

5、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 prior to use.2. Summary of Test Method2.1 Aweighed specimen consisting of two plies a minimumsize of 50-mm 2.0-in. square, oriented in

6、 a 0/ 90 crossplyconfiguration, and sandwiched between bleeder material andrelease film. The sandwich is placed in a platen press heated toeither temperature A, 120C 250F, or temperature B, 175C350F or another specified temperature. The press is closed toprovide a pressure of 700 kPa 100 psi. The pr

7、essure is heldfor 15 min or until the resin gels. The cooled sandwichassembly is removed and the resin that has flowed to the edgesof the specimen is removed and the specimen reweighed. Thechange in weight is expressed as a percent of the originalweight and reported as percent flow.3. Significance a

8、nd Use3.1 This test method is used to obtain the resin flow ofcarbon fiber-epoxy prepreg tape or sheet material. It is suitablefor comparing lots of material of supposedly the same charac-teristics and also for comparative evaluation of materialsproduced by different vendors using different resin-fi

9、ber com-binations.3.2 Composite parts are laminated from prepreg material atvarious pressures and temperatures. Production process designwill require a flow test be run at a temperature and a pressureclose to that of the actual molding conditions. All methods ofmeasuring resin flow are dependent on

10、the size and geometryof the specimen. This test method uses the smallest quantity oftape that will give reproducible results.3.2.1 The percent resin flow of a single fiber and resinsystem at a temperature and pressure varies with the volatilecontent, degree of advancement of epoxy resin, and with th

11、eresin content of the prepreg tape or sheet.3.2.2 As volatile content and degree of resin cure (advance-ment) change with time, this test method is useful in comparingthe life of prepreg tape and sheet.4. Apparatus4.1 Cutting Template, square metal, 50 by 50 mm 2.0 by2.0 in., minimum.4.2 Cutting Tem

12、plate, metal, 100 by 100 mm 4.0 by 4.0in., minimum.4.3 Cutting Knife, single edge.4.4 Analytical Balance capable of weighing to the nearest0.001 g 0.000035 oz.4.5 Glass Bleeder Cloth, Style 1581 or 181.4.6 TFE-Fluorocarbon Coated, Woven Separator Cloth,2porous.4.7 Release Film of 0.03 to 0.06 mm 0.0

13、01 to 0.002 in.thickness polyester, aluminum, etc.4.8 Platen Press, capable of being heated to 175 6 3C 3506 5F and capable of applying 4000 N 900 lbf.5. Interferences5.1 This test method depends on platen force being suppliedevenly to the specimen. For this to be done, the platen mustload evenly ac

14、ross its surface and not point load to the point ofinitial contact. When bleeder materials are used on the top and1This test method is under the jurisdiction of ASTM Committee D30 onComposite Materials and is the direct responsibility of Subcommittee D30.03 onConstituent/Precursor Properties.Current

15、 edition approved Oct. 1, 2011. Published November 2011. Originallyapproved in 1976. Last previous edition approved in 2009 as D3531 99(2009).DOI: 10.1520/D3531_D3531M-11.2DuPont product TX-1040 or equivalent has been found satisfactory for thispurpose.1Copyright ASTM International, 100 Barr Harbor

16、Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.bottom of the specimen, the effect of uneven pressure applica-tion is less pronounced than if no bleeder materials are used.Bleeders tend to minimize pressure effects, since if resin flowsinto the bleeder it will do so within a broa

17、d pressure range.Sometimes, platen pressure needs to be increased gradually toassure even loading.5.2 The platen flatness must be sufficient for the specimen toload evenly. For this reason the specimen thickness should beat least five times the tolerance of platen flatness. Specimensthat do not meet

18、 this requirement should have additional plylayers oriented as a repeating unit of the first two plies.5.3 Ply orientation and coupon size directly affects reportedflow. A sample cut with a ply orientation of 45 will not havethe same reported flow as a sample cut with a ply orientationof 0. This is

19、because flow paths are hindered to a differentdegree based on the different coupon size and orientation.5.4 Temperature should be even across the specimen andwithin the tolerance specified. Temperature influences resinviscosity, which effects flow rate.5.5 Generally, larger coupon sizes reduce later

20、al flow sinceresin has further to travel to the edge of the specimen. Largercoupon sizes do not greatly influence horizontal flow (withbleeders). However, difficulty in coupon handleability in-creases with increasing coupon size. Also small coupon size of50 mm 2.0 in. square is felt to be the minimu

21、m coupon size.A maximum practical size is 100 mm 4.0 in square.5.6 The matching of angles and footprint from one ply to thenext is critical. Flow differences may be found if the ply layersdo not superimpose on top of each other or are aligned with anangle bias.5.7 It is recommended that the heated p

22、latens remain closedunder pressure until resin gelation occurs. Shorter times maycause some of the flowed resin to associate back with thesample rather than the bleeder cloth. Leaving the sample in thepress after gelation has no effect on flow results.6. Test Specimen6.1 A minimum of three specimens

23、 shall be tested for eachsample.6.2 The test specimen shall consist of two plies, one at 0and the other at 90 of 50-mm 2-in. square minimum sizeprepreg sheet.7. Conditioning7.1 Store carbon fiber-epoxy prepreg tape at low tempera-tures, approximately 18C 0F, to prolong the usefulness ofthe material.

24、 Allow the sealed packages of material to warm toambient temperature before the seal is opened to ensure that thematerial does not absorb moisture from the atmosphere.7.2 Do not expose the material, which usually has somevolatile content, at ambient temperature for long periods oftime before testing

25、 is begun.8. Procedure8.1 Cut two pieces 50-mm 61 mm 2.0-in. 6 0.04 in.square, minimum, from the prepreg material. Other sizes maybe used, but the two plies shall match within the tolerencesspecified.8.2 Crossply the pieces at 0 to 90 and weigh to nearest0.001 g 0.000035 oz, recording the weight as

26、W1.8.3 Cut four pieces of Style 1581 glass bleeder cloth of atleast four times the area of the prepeg sample, 100 by 100 mm4.0 by 4.0 in. square, minimum.8.4 Cut two pieces of porous TFE-fluorocarbon separatorcloth to the same size as the bleeder cloth, 100 by 100 mm 4.0by 4.0 in. square, minimum.8.

27、5 Cut two pieces of release film minimum of 150 mm 6.0in. square.8.6 Prepare the specimen assembly as follows:8.6.1 Place a 150- by 150-mm 6.0- by 6.0-in. square pieceof release film on a clean work surface.8.6.2 Apply two pieces of bleeder cloth centered upon the150-mm 6.0-in. square of release fil

28、m.8.6.3 Place one piece of porous separator cloth on top of andwith the edges aligned to the edges of the glass bleeder cloth.8.6.4 Place the 50-mm 2.0-in. square test specimen on thecenter and parallel with the edges of the porous separator cloth.8.6.5 Cover the specimen with another piece of porou

29、sseparator cloth.8.6.6 Cover the assembly with two pieces of the bleedercloth aligned with the edges.8.6.7 Complete the assembly by covering it with a 150-mm6.0-in. square piece of release film. All edges should bealigned and centered on the sheets.8.6.8 Weigh the specimen assembly to nearest 0.001

30、g0.000035 oz and record as W2.8.6.9 Insert the assembly into a platen press preheated toeither of the test temperatures (A or B) 63C 65F or anyother temperature specified. Record the actual platen tempera-tures. Cure this assembly for the gel time recommended by thematerial supplier. Apply pressure

31、of 700 670 kPa 100 6 10psi within5sofclosing platens and starting timer. Cure thisassembly for the gel time recommended by the materialsupplier.8.6.10 Remove the layup assembly from the press.8.6.11 Allow assembly to cool to room temperature, re-weigh to nearest 0.001 g 0.000035 oz, record as W3.8.6

32、.12 Separate the resin saturated bleeder materials fromthe composite specimen. Use care in separating the separatormaterial and the specimen to avoid loss of fiber material.8.6.13 Reweigh the specimen to the nearest 0.001 g0.000035 oz and record as W4.9. Calculation9.1 Calculate the resin flow, RF,

33、as a weight percent of theoriginal prepreg specimen as follows:RF,%5W12 W4W13 100 (1)where:W1= weight of the prepreg specimen, g oz andW4= weight of the specimen after flow test, g oz.9.2 Alternatively the resin flow may be calculated as aweight percentage of the volatile-free prepreg, namely:RF vol

34、atile2free!,%5W12 W22 W3! 2 W4W12 W22 W3!3 100 (2)D3531/D3531M 112where:W2= original weight of specimen assembly, g oz andW3= weight of specimen assembly after heating, g oz.10. Report10.1 The report shall include the following:10.1.1 Complete identification of the material, including thefiber type,

35、 fiber manufacturer, fiber treatment, resin identifica-tion, resin manufacturer, and manufacturer of the prepregmaterial,10.1.2 Ply orientation and stacking sequence,10.1.3 The resin flow in weight percent for each specimenand the average resin flow,10.1.4 The actual test temperature,10.1.5 The cure

36、 time used, and,10.1.6 Deviations to this method if any.11. Precision and Bias11.1 PrecisionThe precision, defined as the degree ofmutual agreement between individual measurements, can beestimated from the results of a round robin conducted onsamples of prepreg by four laboratories, each laboratorym

37、aking three measurements on each sample. The coefficient ofvariation for the total of twelve measurements having a meanresin flow of 26.1 % was 11.2 %. No modern measure ofprecision is available.11.2 BiasNo estimate of bias can be offered as noaccepted reference level is available.12. Keywords12.1 c

38、arbon fiber-epoxy prepreg; resin flowASTM International takes no position respecting 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 ri

39、skof 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 andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of th

40、is 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, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake

41、 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). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).D3531/D3531M 113