ASTM D1644-2001(2006) Standard Test Methods for Nonvolatile Content of Varnishes《清漆中不挥发物含量的标准试验方法》.pdf
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1、Designation: D 1644 01 (Reapproved 2006)Standard Test Methods forNonvolatile Content of Varnishes1This standard is issued under the fixed designation D 1644; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision
2、. 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. Scope1.1 These test methods determine the fraction of a va
3、rnishthat is nonvolatile at the temperature of the test while volatilesolvents are driven off. It is sometimes an approximatemeasure of the film-forming matter in a varnish.1.2 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.
4、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 prior to use. For a specificst
5、atement, see Section 3.2. Significance and Use2.1 These test methods are applicable to varnish and areuseful to producers and users in determining nonvolatilecontent and are sometimes an appropriate measure of thefilm-forming matter in varnish.3. Hazards3.1 Since the flash points of some of the solv
6、ents used incoatings and related products are below the temperature of thetest, care should be exercised that the lower explosive limits ofthe solvents are not exceeded. The amount of solvent in theoven atmosphere at any one time will depend on the number oftests (pans) in the oven, the percent nonv
7、olatile of the samples,the size of the oven, the type of oven (mechanical or gravityconvection) and the air changes per hour.TEST METHOD A3 h AT 105C4. Procedure4.1 Place a portion of the thoroughly mixed sample in astoppered bottle, or alternatively, in a weighing pipet or a10-mL syringe without a
8、needle, and from this weigh bydifference 1.2 6 0.1 g into a tared flat-bottomed metal or glassdish (Note 1), 80 to 100 mm in diameter and 5 to 10 mm indepth, such as friction-top can covers, ointment boxes, or petridishes.NOTE 1The term “tared, flat-bottomed dish” implies that the emptydish has no m
9、easurable weight change when subjected to the same heatschedule as prescribed for the dish containing the specimen. If this isfound to be not so, then more suitable vessels must be found, orcorrections applied.4.2 By gentle tilting, spread the specimen over the bottom ofthe dish and heat for3hinaven
10、tilated oven maintained at 1056 2C. If necessary, a piece of stout wire can be included in thetare of the dish and used at intervals to break up skins bystirring during the heating period. Cool in a desiccator andweigh the dish.5. Calculation5.1 Calculate the percent of nonvolatile matter NV asfollo
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