ASTM C544-2003(2013) 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

《ASTM C544-2003(2013) 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》由会员分享，可在线阅读，更多相关《ASTM C544-2003(2013) 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（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: C544 03 (Reapproved 2013)Standard Test Method forHydration of Dead Burned Magnesite or Periclase Grain1This standard is issued under the fixed designation C544; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year

2、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 measurement of the relativeresistance of magnesia grain to hydration.1.2 This standard

3、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.2. Referenced Documents2.1 ASTM S

4、tandards:2C92 Test Methods for Sieve Analysis and Water Content ofRefractory MaterialsC357 Test Method for Bulk Density of Granular RefractoryMaterialsC456 Test Method for Hydration Resistance of Basic Bricksand ShapesC493 Test Method for Bulk Density and Porosity of Granu-lar Refractory Materials b

5、y Mercury Displacement (Dis-continued 2002) (Withdrawn 2002)33. 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

6、 taken in interpreting the data.4. Apparatus4.1 Autoclave, 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 C456.4.2 Standard Sieves, ASTM No. 6 (3.

7、35 mm), No. 12 (1.70mm), No. 20 (850 m), No. 40 (425 m), and No. 50 (300 m).NOTE 2The equivalent Tyler Standard Series sieves described in TestMethods C92 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 sie

8、ve to obtain themaximum amount of coarse material. 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:Passin

9、g Sieve No. Retained on Sieve No.6 (3.35 mm) 12 (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 ea

10、ch 5-h test,but not enough to permit contact with 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 (

11、105 to110C) for at least 2 h.5.6 Place the preheated 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 autoclav

12、e to 80 psi (552 kPa) at 324F(162C) in a total time 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

13、 reduce the autoclave toatmospheric pressure in 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 onRefractori

14、es and is the direct responsibility of Subcommittee C08.04 on ChemicalBehaviors.Current edition approved April 1, 2013. Published August 2013. Originallyapproved in 1964. Last previous edition approved in 2008 as C544 03 (2008).DOI: 10.1520/C0544-03R13.2For referenced ASTM standards, visit the ASTM

15、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.3The last approved version of this historical standard is referenced onwww.astm.org.Copyright ASTM Internati

16、onal, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States15.8 Place each specimen with the cover and the pan on a No.50 (300-m) sieve, and screen according to Test Methods C92for dry sieve analysis. Weigh the amount of material retainedon the No. 50 sieve. Record the

17、individual specimen weight, H.6. Calculation and Report6.1 Calculate the percentage hydration as follows:hydration, % 5 G 2 H!/G# 3100where:G = weight 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 e

18、ach specimen as thepercentage of material passing the No. 50 (300-m) sieve afterthe hydration test.7. Precision and Bias7.1 Interlaboratory Study:7.1.1 An interlaboratory test program between six laborato-ries was conducted. Each laboratory tested four magnesiamaterials. Each of the four magnesia ma

19、terials was tested fourtimes. Typical chemical analyses and bulk specific gravity dataon the four magnesia materials appear in Table 1.47.1.2 No ruggedness test was run on this test method priorto conducting the interlaboratory study.7.2 Precision:7.2.1 RepeatabilityThe maximum permissible differenc

20、edue to test error between two test results obtained by oneoperator on the same material is given by the repeatabilityinterval and the relative repeatability interval (coefficient ofvariation). The 95 % repeatability intervals are given in Table2. Two test results that do not differ by more than the

21、repeatability interval will be considered to be from the samepopulation, and, conversely, two test results that do differ bymore than the repeatability interval will be considered to befrom different populations.7.2.2 ReproducibilityThe maximum permissible differ-ence due to test error between two t

22、est results obtained by twooperators in different laboratories on the same type of materialusing the same type of test equipment is given by thereproducibility interval and relative reproducibility interval(coefficient of variation). The 95 % reproducibility intervalsare given in Table 2. Two test r

23、esults that do not differ by morethan the reproducibility interval will be considered to be fromthe same population, and, conversely, two test results 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 i

24、tself to a state-ment of bias.8. Keywords8.1 autoclave; grain; hydration resistance; magnesite; peri-clase; refractories4These data were not measured on the actual samples tested in the hydration test,but are representative of the materials used in the interlaboratory study.TABLE 1 Material Properti

25、esMaterial 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 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.

26、0 100.0 100.0 99.9Bulk Specific Gravity:By Water Displacement(ASTM C357). . . . . . 3.21 3.32By Mercury Displacement(ASTM C493)3.36 3.15 3.27 3.37C544 03 (2013)2ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this sta

27、ndard. 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 committee and must be revi

28、ewed 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 a meeting of theresponsib

29、le 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 Drive, PO Box C700, West Co

30、nshohocken, 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 t

31、o photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).TABLE 2 Repeatability and Reproducibility DataMaterialNumberAverage, XStandardWithin, SrDeviationBetween, SRRepeatabilityInterval, rReproducibilityInterval, RCoefficient of Variation 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 32.92C544 03 (2013)3