1、Designation: D 3312 04An American National StandardStandard Test Method forPercent Reactive Monomer in Solventless Varnishes1This standard is issued under the fixed designation D 3312; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision
2、, 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.1. Scope1.1 This test method covers the determination of the percentof volatile reactive monomer having a vapor pre
3、ssure exceed-ing 13.3 Pa (0.1 Torr) at 25 C in an uncatalyzed solventlessvarnish. Experience has shown this method does not accuratelydetermine percent reactive monomer when the vapor pressureis less than 13.3 Pa (0.1 Torr).1.2 The values stated in SI units are the standard. The valuesgiven in paren
4、theses are for information only.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 limitati
5、ons prior to use. For a specificprecaution, see Section 5.NOTE 1There is no similar or equivalent ISO/IEC standard.2. Referenced Documents2.1 ASTM Standards:2D 1711 Terminology Relating to Electrical InsulationD 5423 Specification for Forced-Convection LaboratoryOvens for Evaluation of Electrical In
6、sulation33. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 reactive monomer, nin solventless electrical varnish,a substance, that, when added to a resin, will combinechemically with that resin under specified conditions.3.2 See Terminology D 1711 for definitions of other termsre
7、lating to electrical insulation.4. Significance and Use4.1 The percent of reactive monomer in solventless var-nishes will affect the viscosity, the handling, and the processingproperties of the uncured resin. The percent of reactivemonomer will possibly affect the degree of hardness andshrinkage whi
8、ch in turn will affect the physical and electricalproperties of the cured resin.5. Safety Precautions5.1 It is unsafe to use varnish at temperatures above theflash point without adequate ventilation, especially if thepossibility exists that flames or sparks are present. Storevarnish in sealed contai
9、ners.6. Apparatus6.1 Balance, capable of weighing to nearest 0.0001 g.6.2 ThermometerA glass thermometer having a rangefrom 0 to 200 C (30 to 400 F) and accurate within 6 1C(62 F).6.3 OvenA forced-draft constant-temperature oven con-forming to Specification D 5423, Type II.6.4 Bottle and Drying Dish
10、esA stoppered bottle andflat-bottom aluminum drying dish. having an inside diameter ofapproximately 70 mm (234 in.) and a depth of 8 mm (516 in.).6.5 DesiccatorA suitable desiccator containing anhydrouscalcium chloride (CaCl2).7. Test Specimens7.1 Preparing SpecimensPlace a portion of the uncata-lyz
11、ed solventless varnish in a stoppered bottle and weigh.Transfer a specimen weighing between 0.2 and 0.3 g from theweighed stoppered bottle to a weighed drying dish, which hasbeen previously heated for 30 min at 150 C (300 F) andcooled in a desiccator. Weigh the stoppered bottle with theremaining con
12、tents again. Determine the exact weight of thespecimen transferred to the drying dish by the difference inweight of the stoppered bottle. Prepare two specimens from thecontents of the stoppered bottle.8. Procedure8.1 Dilution of SpecimensAdd 5 6 1 mL of methylisobutyl ketone (MIBK) to each specimen
13、in the drying dish.Mix the specimen and the MIBK by moving the drying dishesin a circular direction. Mixing on a hot plate at temperaturesbelow 65 C (150 F) is permissible. Take care to prevent anyloss of solvent or specimen by spillage.1This test method is under the jurisdiction of ASTM Committee D
14、09 onElectrical and Electronic Insulating Materials and is the direct responsibility ofSubcommittee D09.01 on Electrical Insulating Varnishes, Powders, and Encapsu-lating Compounds.Current edition approved Sept. 1, 2004. Published September 2004. Originallyapproved in 1974. Last previous edition app
15、roved in 2000 as D 3312 00.2For referenced ASTM standards, visit the ASTM website, 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.3Withdrawn.1Copyright ASTM Interna
16、tional, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.8.2 Drying SpecimensPlace the specimens in constant-temperature oven which has been stabilized at 150 C (300 F)within 15 min after mixing. Keep the specimens in the 150 C(300 F) oven for 15 min.8.3 Weighing D
17、ried SpecimensAt the termination of the15-min heating period, remove the specimens to a desiccatorand cool to room temperature. Weigh each specimen immedi-ately upon removal from the desiccator.9. Calculation9.1 Calculate the percentage of monomer by weight as aratio of the weight loss of the dried
18、specimen to the weight ofthe specimen in the original state, expressed as a percentage, asfollows:% monomer 5 weight loss/original sample weight! 3 100 (1)10. Report10.1 Report the following information:10.1.1 Identification of the solventless varnish, and10.1.2 Percent reactive monomer.11. Precisio
19、n and Bias11.1 PrecisionThe interlaboratory standard deviation cal-culated from the results of testing in six laboratories is asfollows:4Monomer Interlaboratory Standard Deviation (%)Styrene 0.365Vinyl toluene 0.163t-butyl styrene 1.61Diallyl phthalate 1.9911.2 BiasThis test method has no bias, sinc
20、e the value forpercent reactive monomer is determined solely in terms of thistest method.12. Keywords12.1 monomer (See reactive monomer); reactive monomer;reactive monomer, %; solventless varnish; varnishASTM International takes no position respecting the validity of any patent rights asserted in co
21、nnection 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 the respo
22、nsible 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 careful
23、 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 International,
24、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).4Supporting data are available from ASTM Headquarters. Request RR: D-9-1013.D3312042
