ASTM C1016-2002(2008)e1 Standard Test Method for Determination of Water Absorption of Sealant Backing (Joint Filler) Material《密封剂(填缝料)吸水率的测定的标准试验方法》.pdf

《ASTM C1016-2002(2008)e1 Standard Test Method for Determination of Water Absorption of Sealant Backing (Joint Filler) Material《密封剂(填缝料)吸水率的测定的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM C1016-2002(2008)e1 Standard Test Method for Determination of Water Absorption of Sealant Backing (Joint Filler) Material《密封剂(填缝料)吸水率的测定的标准试验方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: C1016 02 (Reapproved 2008)1Standard Test Method forDetermination of Water Absorption of Sealant Backing(Joint Filler) Material1This standard is issued under the fixed designation C1016; the number immediately following the designation indicates the year oforiginal adoption or, in the ca

2、se of 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.1NOTEAdded research report information to Section 13 editorially in September 2010.1. Scope1.1 This te

3、st method covers a laboratory procedure fordetermining the water absorption characteristics of sealantbacking and joint filler materials, hereinafter referred to asbacking.1.2 The values stated in SI units are to be regarded as thestandard. The inch-pound units in parentheses are for informa-tion on

4、ly.1.3 The committee with jurisdiction over this standard is notaware of any comparable standards published by other ASTMcommittees or other organizations.1.4 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of

5、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:2C717 Terminology of Building Seals and Sealants3. Terminology3.1 DefinitionsRefer to Terminology C717 for the follow-

6、ing terms used in this test method: joint filler, sealant, andsealant backing.4. Summary of Test Method4.1 The mass of three measured specimens of backing isdetermined. The specimens are then placed in room tempera-ture water for 24 h after which the specimens are removed fromthe water and their mas

7、s measured. The change in mass iscalculated, and the result is expressed as a change in mass perunit of volume.4.2 Procedure A measures the maximum amount of waterthat can enter the backing. Procedure B measures the amountof water that can enter the backing with the backing cut endssealed.5. Signifi

8、cance and Use5.1 This test method determines the amount of water ab-sorbed by a backing material. Water absorption by the backingmay affect sealant performance.5.2 This test method is also useful when designating properstorage of back up material and in determining appropriateprecautions when using

9、backing materials.5.3 The specifier, using this test method, can exercisejudgment in the selection of backing materials based on waterabsorption characteristics.6. Apparatus6.1 Balance, sensitive to 0.1 g (0.004 oz).6.2 Rule, steel, graduated to 1.0 mm (;116 in.).6.3 Shallow Pan for Water, at least

10、50 mm (2 in.) deep and350 mm (14 in.) long.6.4 Paraffn Wax.7. Sampling7.1 Take samples from manufactured product. The numberof samples for each lot shall be agreed upon between thepurchaser and the seller. A sample shall consist of three testspecimens.1This test method is under jurisdiction of ASTM

11、Committee C24 on BuildingSeals and Sealants and is the direct responsibility of Subcommittee C24.20 onGeneral Test Methods.Current edition approved May 1, 2008. Published June 2008. Originallyapproved in 1984. Last previous edition approved in 2002 as C1016 02. DOI:10.1520/C1016-02R08E01.2For refere

12、nced 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.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West

13、Conshohocken, PA 19428-2959, United States.7.2 Sample selection is important, therefore, the sampleshould be representative of typical backing production. Careshould be exercised in choosing samples that have not beendamaged by inappropriate storage or handling.7.3 Samples should be of uniform shape

14、 for their length toenable accurate calculation of volume.8. Test Specimens8.1 A test specimen is a piece of backing 300 6 5mm(126 0.25 in.) in length. Ideally the cross-sectional backing areashould be from 2 to 3 cm2(0.3 to 0.5 in.2). Cut three testspecimens from each sample.9. Conditioning9.1 Cond

15、ition the test specimens at 23 6 2C (73 6 3F)and 50 6 5 % relative humidity for a minimum of 24 h priorto testing, provided the specimens feel and appear dry. Speci-mens that appear damp should be dried in accordance with themanufacturers recommendations before the 24 h conditioningperiod starts.10.

16、 Procedure10.1 Procedure A:10.1.1 Measure the mass of each conditioned specimen tothe nearest 0.1 g (0.004 oz) and record.10.1.2 Measure and record the length of each specimen tothe nearest 1 mm (116 in.).10.1.3 Measure and record the appropriate end dimensionsof each specimen to the nearest 1 mm (1

17、16 in.), to permit across-sectional area calculation.10.1.3.1 The procedures in 10.1.2 and 10.1.3 are critical tothe precision and bias of the test. Care is required to obtainaccurate measurements.10.1.4 Submerge the entire specimen in water in a shallowpan. Secure the specimen so the top side in th

18、e long dimension,is approximately 25 mm (1 in.) below surface.10.1.5 After immersion for 24 h, remove the specimen bypicking it up 3 in. (75 mm) from the ends and place itimmediately on the weighing platform. Do not press or squeezethe specimen. Within the next 1 min, record the mass of thespecimen.

19、 Within the next 1 min, record the mass of thespecimen to the nearest 0.1 g (0.004 oz).10.1.5.1 The weighing platform on the balance should belarge enough to support the entire specimen and serve as a trayto catch any water that may leave the specimen during massdetermination.10.2 . Procedure B:10.2

20、.1 Measure and record the length of each specimen tothe nearest 1 mm (116 in.).10.2.2 Measure and record the appropriate end dimensionsof each specimen to the nearest 1 mm (116 in.), to permit across-sectional area calculation.10.2.2.1 The procedures in 10.2.1 and 10.2.2 are critical tothe precision

21、 and bias of the test. Care to obtain accuratemeasurements is required.10.2.3 Dip the cut ends of the specimen to a depth of 3.0mm (18 in.) in melted paraffin wax at 65 6 5C, remove and letcool. Repeat the dipping three times until the ends arecompletely sealed by approximately 1 mm (116 in.) of par

22、affinwax on each cut end.10.2.4 After the wax cools, measure the mass of eachconditioned specimen to the nearest 0.1 g (0.004 oz) andrecord.10.2.5 Submerge the entire specimen in water in a shallowpan. Secure the specimen so the top side, in the long dimen-sion, is approximately 25 mm (1 in.) below

23、the surface.10.2.6 After immersion for 24 h, remove the specimen bypicking it up 3 in. (75 mm) from the ends and place itimmediately on the weighing platform. Do not press or squeezethe specimen. Within the next 1 min, record the mass of thespecimen to the nearest 0.1 g (0.004 oz).10.2.6.1 The weigh

24、ing platform should be large enough tosupport the entire specimen and serve as a tray to catch anywater that may leave the specimen during mass determination.11. Calculation11.1 Calculate each specimens dry cross-sectional area (A0)using the appropriate formula for the geometry of the cross-section

25、shape.11.2 Calculate the dry, original volume, (V0), as follows:V05 103 A0where:V0= original dry volume, cm3(in.3),A0= cross-sectional area cm2(in.2), and10= original length, cm (in.).11.3 Calculate water absorption as a mass per unit volumefor each specimen as follows:W 5m02 m1V0where:W = water abs

26、orption, g/cm3(oz/in.3),m1= initial mass, g (oz),m0= final mass, g (oz), andV0= initial dry volume, cm3(in.3)11.4 For purposes of calculation it is assumed that, at 23 62C (73 6 3F) and atmospheric pressure, 1 g (0.035 oz) ofwater occupies 1 cm3(0.061 in.3) in volume.11.5 Calculate the sample averag

27、e water absorption asfollows:Wa5W11 W21 W33where:Wa= average water absorption, g/cm3(oz/in.3),W1= Specimen 1 water absorption, g/cm3(oz/in.3),W2= Specimen 2 water absorption, g/cm3(oz/in.3), andW3= Specimen 3 water absorption, g/cm3(oz/in.3).12. Report12.1 Report the following information:12.1.1 Nam

28、e and description of the tested backing material,12.1.2 Date of receipt of the backing material,12.1.3 Procedure A or B, and12.1.4 Individual specimen and sample average water ab-sorption values.C1016 02 (2008)1213. Precision and Bias313.1 These data were developed using 1.59 cm (58 in.)diameter clo

29、sed cell, open cell, and soft-type backing material,therefore results may vary with different diameter backingmaterials.13.1.1 Procedure A:13.1.1.1 The repeatability (within a given laboratory) inter-val for three materials tested by four laboratories is 0.044g/cm3(0.025 oz/in.3). In future use of t

30、his test method, thedifference between two test results obtained in the samelaboratory on the same material will be expected to exceed0.044 g/cm3(0.025 oz/in.3) only about 5 % of the time.13.1.1.2 The reproducibility (between given laboratories)interval for three materials tested by four laboratorie

31、s is 0.387g/cm3(0.222 oz/in.3). In future use of this test method, thedifference between test results obtained in a different labora-tory on the same material will be expected to exceed 0.387g/cm3(0.222 oz/in.3) only about 5 % of the time.13.1.2 Procedure B:13.1.2.1 The repeatability (within a given

32、 laboratory) inter-val for three materials tested by four laboratories is 0.024g/cm3(0.014 oz/in.3). In the future use of this test method, thedifference between two test results obtained in the samelaboratory on the same material will be expected to exceed0.024 g/cm3(0.014 oz/in.3) only about 5 % o

33、f the time.13.1.2.2 The reproducibility (between given laboratories)interval for three materials tested by four laboratories is 0.387g/cm3(0.217 oz/in.3). In future use of this test method, thedifference between two test results obtained in a differentlaboratory on the same material will be expected

34、 to exceed0.387 g/cm3(0.217 oz/in.3) only about 5 % of the time.14. Keywords14.1 sealant; sealant backing; water absorptionASTM 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 expr

35、essly 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 committee and must be reviewed every five years andif not revise

36、d, 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 a meeting of theresponsible technical committee, which you may

37、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 Drive, PO Box C700, West Conshohocken, PA 19428-2959,United State

38、s. 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/).3Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Report RR:C24-1014 and RR:C24-1037.C1016 02 (2008)13