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本文(ASTM C544-2003 Standard Test Method for Hydration of Dead Burned Magnesite or Periclase Grain《僵烧镁砂或方镁石颗粒水合作用的标准试验方法》.pdf)为本站会员(wealthynice100)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM C544-2003 Standard Test Method for Hydration of Dead Burned Magnesite or Periclase Grain《僵烧镁砂或方镁石颗粒水合作用的标准试验方法》.pdf

1、Designation: C 544 03Standard Test Method forHydration of Dead Burned Magnesite or Periclase Grain1This standard is issued under the fixed designation C 544; 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.1. Scope1.1 This test method covers the measurement of the relativeresistance of magnesia grain to hydration.1.2 This standard does not purpor

3、t 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.2. Referenced Documents2.1 ASTM Standards:2C 92

4、Test Methods for Sieve Analysis and Water Content ofRefractory MaterialsC 357 Test Method for Bulk Density of Granular RefractoryMaterialsC 456 Test Method for Hydration Resistance of BasicBricks and ShapesC 493 Test Method for Bulk Density and Porosity of Granu-lar Refractory Materials by Mercury D

5、isplacement3. Significance and Use3.1 This test method determines relative hydration resis-tance of magnesia grain.3.2 This test method is used in industry to evaluate grainsamples and is used for specification purposes in some cases.3.3 Care must be taken in interpreting the data.4. Apparatus4.1 Au

6、toclave, suitable for operation at 80 psi (552 kPa) at324F (162C) and equipped with pressure- and temperature-measuring devices and safety equipment.NOTE 1A suitable apparatus is shown in Fig. 1 of Test Method C 456.4.2 Standard Sieves, ASTM No. 6 (3.35 mm), No. 12 (1.70mm), No. 20 (850 m), No. 40 (

7、425 m), and No. 50 (300 m).NOTE 2The equivalent Tyler Standard Series sieves described in TestMethods C 92 may be substituted for the ASTM sieves.5. Procedure5.1 Remove the material retained on a No. 6 (3.35-mm)sieve, and crush it to pass the No. 6 sieve to obtain themaximum amount of coarse materia

8、l. Recombine with theportion passing the No. 6 sieve, and screen the resultant sampleto remove all material passing a No. 40 (425-m) sieve. Ifnecessary, dry at 220 to 230F (105 to 110C).5.2 Separate this sample into the following three fractions:Passing Sieve No. Retained on Sieve No.6 (3.35 mm) 12

9、(1.70 mm)12 (1.70 mm) 20 (850 m)20 (850 m) 40 (425 m)5.3 Prepare a 100-g specimen by using equal parts byweight of the three sizes listed in 5.2.5.4 Add sufficient water to the autoclave to maintain 80 psi(552 kPa) at 324F (162C) for the duration of each 5-h test,but not enough to permit contact wit

10、h any of the specimens.5.5 Place each weighed specimen in a No. 3 porcelaincrucible, and cover with a loosely crimped piece of aluminumfoil to protect the specimen from drip or condensate. Dry thecovered crucibles in a forced-air dryer at 220 to 230F (105 to110C) for at least 2 h.5.6 Place the prehe

11、ated rack containing the specimens in theautoclave. Heat the autoclave with the pressure-release valveopen; after a steady flow of steam is obtained through thevalve, continue to purge for 3 min to remove all air, close thevalve, and bring the autoclave to 80 psi (552 kPa) at 324F(162C) in a total t

12、ime of 1 h. Maintain the autoclave at 80 65 psi (552 6 35 kPa) and 324 6 4F (162 6 2C) for 5 h.5.7 Allow sufficient cooling to lower the autoclave to 20 to30 psi (138 to 207 kPa) with the release valve closed, and thencarefully open the relief valve to reduce the autoclave toatmospheric pressure in

13、a total time between 30 and 60 min.Remove the specimens and dry to constant weight at 220 to230F (105 to 110C) in a forced-air dryer. Record theindividual specimen weight, G.1This test method is under the jurisdiction of ASTM Committee C08 onRefractories and is the direct responsibility of Subcommit

14、tee C08.04 on ChemicalBehaviors.Current edition approved Nov. 1, 2003. Published December 2003. Originallyapproved in 1964. Last previous edition approved in 1998 as C 544 92 (1998)e1.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm

15、.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, United States.5.8 Place each specimen with the cover and the pan on a No.50

16、(300-m) sieve, and screen according to Test Methods C 92for dry sieve analysis. Weigh the amount of material retainedon the No. 50 sieve. Record the individual specimen weight, H.6. Calculation and Report6.1 Calculate the percentage hydration as follows:hydration, % 5 G 2 H!/G# 3 100where:G = weight

17、 of dried specimen after hydration, g, andH = weight of hydrated specimen retained on a No. 50(300-m) sieve, g.6.2 Report the amount of hydration of each specimen as thepercentage of material passing the No. 50 (300-m) sieve afterthe hydration test.7. Precision and Bias7.1 Interlaboratory Study:7.1.

18、1 An interlaboratory test program between six laborato-ries was conducted. Each laboratory tested four magnesiamaterials. Each of the four magnesia materials was tested fourtimes. Typical chemical analyses and bulk specific gravity dataon the four magnesia materials appear in Table 1.37.1.2 No rugge

19、dness test was run on this test method priorto conducting the interlaboratory study.7.2 Precision:7.2.1 RepeatabilityThe maximum permissible differencedue to test error between two test results obtained by oneoperator on the same material is given by the repeatabilityinterval and the relative repeat

20、ability interval (coefficient ofvariation). The 95 % repeatability intervals are given in Table2. Two test results that do not differ by more than therepeatability interval will be considered to be from the samepopulation, and, conversely, two test results that do differ bymore than the repeatabilit

21、y interval will be considered to befrom different populations.7.2.2 ReproducibilityThe maximum permissible differ-ence due to test error between two test results obtained by twooperators in different laboratories on the same type of materialusing the same type of test equipment is given by thereprod

22、ucibility interval and relative reproducibility interval(coefficient of variation). The 95 % reproducibility intervalsare given in Table 2. Two test results that do not differ by morethan the reproducibility interval will be considered to be fromthe same population, and, conversely, two test results

23、 that dodiffer by more than the reproducibility interval will be consid-ered to be from different populations.7.3 BiasThis test method does not lend itself to a state-ment of bias.8. Keywords8.1 autoclave; grain; hydration resistance; magnesite; peri-clase; refractories3These data were not measured

24、on the actual samples tested in the hydration test,but are representative of the materials used in the interlaboratory study.TABLE 1 Material PropertiesMaterial Number 1234Chemical Analysis (CalcinedBasis), %:Silica (SiO2) 1.0 3.3 0.7 0.55Alumina (Al2O3) 0.5 1.7 0.2 0.2Iron Oxide (Fe2O3) 0.5 3.8 0.2

25、 0.2Chromic Oxide (Cr2O3) . 2.2 . .Lime (CaO) 3.0 11.0 0.7 2.2Boron Oxide (B2O3) . . . . . . 0.03 0.01Magnesia (MgO) 95.0 78.0 98.2 96.75Total, % 100.0 100.0 100.0 99.9Bulk Specific Gravity:By Water Displacement(ASTM C 357). . . . . . 3.21 3.32By Mercury Displacement(ASTM C 493)3.36 3.15 3.27 3.37C5

26、44032ASTM 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 determination of the validity of any such patent rights, and the riskof infringement of such rights

27、, 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 withdrawn. Your comments are invited either for revision of this standard or for additional st

28、andardsand 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 your comments have not received a fair hearing you shouldmake your views known to the ASTM Co

29、mmittee 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 (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveadd

30、ress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org).TABLE 2 Repeatability and Reproducibility DataMaterialNumberAverage, XStandardWithin, SrDeviationBetween, SRRepeatabilityInterval, rReproducibilityInterval, RCoefficient of Var

31、iation RelativeRepeatability,% rRelativeReproducibility,% RWithin Lab,VrBetween Labs,VR1 63.61 2.818 4.447 7.891 12.45 4.430 6.991 12.41 19.572 37.06 3.082 3.811 8.628 10.67 8.316 10.28 23.28 28.793 21.04 3.108 5.947 8.703 16.65 14.77 28.27 41.36 79.134 60.27 6.254 7.085 17.51 19.84 10.38 11.76 29.05 32.92C544033

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