ASTM D1582-1998(2011) Standard Test Method for Nonvolatile Content of Liquid Phenol Resorcinol and Melamine Adhesives《液相苯酚 间苯二酚和三聚氰胺胶粘剂中不挥发物含量的标准试验方法》.pdf

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ASTM D1582-1998(2011) Standard Test Method for Nonvolatile Content of Liquid Phenol Resorcinol and Melamine Adhesives《液相苯酚 间苯二酚和三聚氰胺胶粘剂中不挥发物含量的标准试验方法》.pdf_第1页
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ASTM D1582-1998(2011) Standard Test Method for Nonvolatile Content of Liquid Phenol Resorcinol and Melamine Adhesives《液相苯酚 间苯二酚和三聚氰胺胶粘剂中不挥发物含量的标准试验方法》.pdf_第2页
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1、Designation: D1582 98 (Reapproved 2011)Standard Test Method forNonvolatile Content of Liquid Phenol, Resorcinol, andMelamine Adhesives1This standard is issued under the fixed designation D1582; the number immediately following the designation indicates the year oforiginal adoption or, in the case of

2、 revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers the determination of nonvolatilecontent or total solids of liquid pheno

3、l, resorcinol, andmelamine adhesives with or without hardener (Note 1) addedand containing high-boiling and low-boiling volatile organicsolvents or water, or both.NOTE 1Some low molecular weight materials in the adhesive may belost if hardener is not used. When a hardener is used, it must be mixed i

4、naccordance with the manufacturers instructions.1.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibilit

5、y 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 specificprecautions, see 5.2.2. Referenced Documents2.1 ASTM Standards:2D907 Terminology of Adhesives3. Terminology3.1 DefinitionsMany of

6、the terms in this test method aredefined in Terminology D907.4. Summary of Test Method4.1 Without HardenerA weighed amount of adhesive andquartz sand are oven-dried, cooled in a desiccator, andweighed. The percent nonvolatile content is calculated basedon the amount remaining.4.2 With HardenerA weig

7、hed amount of mixed adhesiveis oven dried, cooled in a desiccator, and weighed. The percentnonvolatile content is calculated based on the amount remain-ing.5. Apparatus5.1 Petri Dish, 100 by 22 mm or its equivalent.5.2 Circulating-Air Oven, capable of maintaining tempera-tures of 70 6 1C, 105 6 1C,

8、and 150 6 1C. (WarningAsafety (explosion-proof) oven should be used when volatilematerials are likely to burn or explode.)5.3 Desiccator, with drying agent and tray.5.4 Analytical Balance, accurate to 1 mg.6. Sampling6.1 Except in special cases, take a composite sample fromthree or more separate con

9、tainers chosen at random. Also, takesamples from containers which appear to be nonrepresentativeand test such samples separately. Place the samples immedi-ately in airtight containers, filled to prevent excessive air spaceabove the adhesive, and take precautions to reduce evaporationor drying to a m

10、inimum. Mix the adhesive in the containerthoroughly if there is a tendency for the materials to separate.6.2 Test three specimens of each sample.7. Procedure7.1 70C Drying Temperature Without Hardener:7.1.1 Place approximately 20 g of the adhesive in a coveredweighing bottle.7.1.2 Place approximatel

11、y 10 g of fine, oven-dried quartzsand in an open Petri dish, together with a small glass stirringrod, and weigh the dish, rod, and contents to the nearest 1 mgon the analytical balance. Weigh out to the nearest 1 mgapproximately2goftheadhesive by difference from theweighing bottle, keeping the bottl

12、e covered as much aspossible. Mix the adhesive and quartz sand intimately bymeans of the stirring rod and distribute uniformly over thebottom of the dish in as thin a layer as possible. Condition thespecimen at 23 6 1C for at least 16 h.1This test method is under the jurisdiction of ASTM Committee D

13、14 onAdhesives and is the direct responsibility of Subcommittee D14.30 on WoodAdhesives.Current edition approved April 1, 2011. Published April 2011. Originallyapproved in 1958. Last previous edition approved in 2004 as D1582 98 (2004).DOI: 10.1520/D1582-98R11.2For referenced ASTM standards, visit t

14、he 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.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,

15、 United States.7.1.3 Place the dish with the rod and contents in the oven at70 6 1C until a constant weight is reached.7.1.4 Place the warm dish immediately in the desiccator andallow to cool to room temperature before weighing to thenearest 1 mg.7.2 70C Drying Temperature With Hardener:7.2.1 Mix ap

16、proximately 100 g of the adhesive in accor-dance with the manufacturers directions, weighing compo-nents to the nearest 0.01 g.7.2.2 Proceed as in 7.1.2, 7.1.3, and 7.1.4.7.3 105C Drying Temperature Without HardenerProceedas in 7.1 except to place the sample in the oven at 105 6 1C.7.4 105C Drying T

17、emperature With HardenerProceed asin 7.2 except to place the sample in the oven at 105 6 1C.7.5 150C Drying Temperature Without HardenerProceedas in 7.1 except to place the sample in the oven at 150 6 1C.7.6 150C Drying Temperature With HardenerProceed asin 7.2 except to place the sample in the oven

18、 at 150 6 1C.8. Calculation8.1 Calculate the percent nonvolatile content or total solidsas follows:Nonvolatile content, % 5wt of residue/wt of specimen!3100(1)The weight of the residue is the difference in the weight ofthe dish, rod, and contents before and after heating.8.2 Repeat the test if the r

19、esults for the three specimens ofa sample do not agree with 60.5 percentage units of oneanother.9. Report9.1 Report the following information:9.1.1 Complete identification of the adhesive tested, includ-ing type, lot number, and source,9.1.2 Procedure used,9.1.3 Catalyst or hardener, mixing proporti

20、ons, and condi-tions used, where applicable,9.1.4 Total drying time to reach constant weight,9.1.5 Number of specimens tested, and9.1.6 Individual nonvolatile content of the three specimensand the average nonvolatile content of the sample.10. Precision and Bias10.1 A precision and bias statement doe

21、s not exist for thistest method because resources necessary for round-robin test-ing have not been forthcoming.11. Keywords11.1 adhesives; melamine; nonvolatile content; phenol;resorcinolASTM International takes no position respecting the validity of any patent rights asserted in connection with any

22、 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 responsible technical

23、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 consideration at

24、 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, 100 Barr Harbor D

25、rive, 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/).D1582 98 (2011)2

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