ASTM D1490-2001(2013) Standard Test Method for Nonvolatile Content of Urea-Formaldehyde Resin Solutions《脲甲醛树脂溶液中非挥发性物质含量的标准测试方法》.pdf

《ASTM D1490-2001(2013) Standard Test Method for Nonvolatile Content of Urea-Formaldehyde Resin Solutions《脲甲醛树脂溶液中非挥发性物质含量的标准测试方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D1490-2001(2013) Standard Test Method for Nonvolatile Content of Urea-Formaldehyde Resin Solutions《脲甲醛树脂溶液中非挥发性物质含量的标准测试方法》.pdf（2页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D1490 01 (Reapproved 2013)Standard Test Method forNonvolatile Content of Urea-Formaldehyde Resin Solutions1This standard is issued under the fixed designation D1490; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the

2、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. Scope*1.1 This test method covers the determination of the appar-ent nonvolatile content of urea-formaldehyde resin sol

3、utionsintended for use as wood adhesives. Due to the chemical natureof such resins, the nonvolatile content determined variesmarkedly according to the type of test used. In order tominimize this condition, this test method is designed to yieldreasonably uniform agreement among different laboratories

4、testing specimens from the same sample.1.2 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.3 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the

5、 user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D907 Terminology of Adhesives3. Terminology3.1 DefinitionsMany terms in this test method are definedin Termi

6、nology D907.4. Significance and Use4.1 Wood adhesive performance and cost is often related tothe solids level (nonvolatile content).4.2 This test method determines the apparent nonvolatilecontent for urea-formaldehyde resins.5. Apparatus5.1 Analytical Balance, accurate to 61.0 mg.5.2 ThermometerA gl

7、ass thermometer having a rangefrom 0 to 110 or 150C (32 to 230 or 302F) and accurate to61C (62F) at the required immersion.5.3 Constant-Temperature Oven, capable of maintaining atemperature of 105 6 1C (221 6 2F) and an air turnover of15 to 17 times per min. Use only one shelf for supporting thespec

8、imens. Position this shelf in the upper third of the oven, asnear one third from the ceiling as possible. Level the shelf towithin 0.025 mm from edge to edge in all directions. Place thethermometer bulb as close to the center of the shelf as possible.5.4 Tared Lunge Weighing Pipet, stoppered weighin

9、g bottle,or equivalent dispenser for accurately weighing by difference.5.5 Drying Dishesluminum foil dishes, with 57 to 58-mminside diameter and 17 mm deep, with flat bottoms, having atolerance of 60.076 mm.5.6 Desiccator, with tray, containing active anhydrous cal-cium chloride desiccant.6. Samplin

10、g6.1 Take a sufficient quantity of the resin lot being evaluatedto conduct the test. While the test consumes less than 10 g ofresin, a sample of approximately 0.23 L (12 pt) is suggested toensure that it is representative and will permit rechecks, ifnecessary. Record the lot number of the resin bein

11、g used.6.2 As urea-formaldehyde resin solutions have a varyingtendency toward mild settling or stratification, agitate the resinthoroughly before sampling, and mix the sample well before itis used in the test.7. Procedure7.1 Preparation of Test SpecimensPlace a portion of thesample in the weighing d

12、ispenser and weigh to 61.0 mg.Transfer a sufficient amount of the sample to yield 0.45 6 0.05g of dried residue, to a tared drying dish which has beenpreviously dried for1hat1056 1C (221 6 2F), and cooledand held in the desiccator until time of use. Reweigh thedispenser and determine, by difference

13、to 61.0 mg, the exactweight of the specimen transferred to the drying dish. Preparea total of three such specimens from the contents of theweighing dispenser. Pipet 5 mL (0.01 pt) of water into eachtared drying dish and mix the water and resin thoroughly bygently rotating the dish.1This test method

14、is under the jurisdiction of ASTM Committee D14 onAdhesives and is the direct responsibility of Subcommittee D14.30 on WoodAdhesives.Current edition approved May 1, 2013. Published May 2013. Originallyapproved in 1957. Last previous edition approved in 2006 as D1490 01 (2006).DOI: 10.1520/D1490-01R1

15、3.2For 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.*A Summary of Changes section appears at the end of this st

16、andardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States17.2 Drying the SpecimensPlace the drying dishes contain-ing the diluted specimens in the temperature oven, previouslyadjusted to 105 6 1C (221 6 2F) with the oven vents and airflow

17、 adjusted to maintain an air turnover of 16 6 1 times permin. Do this within 30 min after the specimens have beenplaced in the dishes. Open the oven door for the minimumpracticable time (never longer than 15 s). Place the dishes onthe shelf, which has been positioned in accordance with 5.3,grouping

18、them about the center in the vicinity of the thermom-eter bulb. The dishes remain in the oven for a total of 3 h 65min.7.3 Weighing the Dried SpecimensRemove the dishescontaining the dried specimens from the oven after the 3-hdrying period in accordance with 7.2, place them in thedesiccator, and coo

19、l to room temperature for at least 5, but notmore than 15 min. Then remove them from the desiccator andimmediately weigh each specimen to 61.0 mg. Discard thedishes after their first use.8. Calculation8.1 Calculate the percent of nonvolatile matter as follows:Nonvolatile matter, % 5 A/B! 3100where:A

20、 = weight of dish containing dried residue, less taredweight of dish, andB = weight of dispenser before specimen is removed, lessweight of dispenser after specimen is removed.9. Report9.1 Report the following information:9.1.1 Date of test,9.1.2 Laboratory where test is performed,9.1.3 Manufacturers

21、 code number and lot number of resintested,9.1.4 Designation of test,9.1.5 Individual and average nonvolatile values obtained,%, and9.1.6 Any conditions that deviated from those prescribed inthis test method.10. Precision and Bias10.1 The precision and bias statement for this test methodhas not been

22、 determined yet. Results are being expected byApril 2003.11. Keywords11.1 nonvolatile content; urea-formaldehydeSUMMARY OF CHANGESSubcommittee D14.30 has identified the location of selected changes to this standard since the last issue,(D1490 961), that may impact the use of this standard. (Approved

23、 October 10, 2001.)(1) Deleted the definitions in Section 3 as they can be found inTerminology D907.(2) Terminology was corrected in Sections 6 and 7 to reflectthat:(a) Resin refers to the lot of material being tested.(b) Sample refers to the amount of material taken from theresin and will be used d

24、uring the testing.(c) Specimen refers to the material placed in the individualtared drying dishes.ASTM 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 determ

25、ination 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 committee and must be reviewed every five years andif not revised, either reapproved or w

26、ithdrawn. 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 a meeting of theresponsible technical committee, which you may attend. If you feel that

27、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 Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (s

28、ingle 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/).D1490 01 (2013)2