ASTM C832-2000(2015) Standard Test Method of Measuring Thermal Expansion and Creep of Refractories Under Load《测量在负荷作用下耐火材料的热膨胀和蠕变的标准试验方法》.pdf

《ASTM C832-2000(2015) Standard Test Method of Measuring Thermal Expansion and Creep of Refractories Under Load《测量在负荷作用下耐火材料的热膨胀和蠕变的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM C832-2000(2015) Standard Test Method of Measuring Thermal Expansion and Creep of Refractories Under Load《测量在负荷作用下耐火材料的热膨胀和蠕变的标准试验方法》.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: C832 00 (Reapproved 2015)Standard Test Method ofMeasuring Thermal Expansion and Creep of RefractoriesUnder Load1This standard is issued under the fixed designation C832; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision,

2、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 procedure for measuring thelinear change of refractory specimens that are subj

3、ected tocompressive stress while being heated and while being held atelevated temperatures.1.2 This test method does not apply to materials whosestrength depends on pitch or carbonaceous bonds unlessappropriate atmospheric control is used (see 7.3).1.3 The values stated in inch-pound units are to be

4、 regardedas standard. The values given in parentheses are mathematicalconversions to SI units that are provided for information onlyand are not considered standard.1.4 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:2E691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test Method3. Terminolo

6、gy3.1 Definitions of Terms Specific to This Standard:3.1.1 maximum dilationthe percent expansion where thethermal-expansion rate equals the creep-deformation rate. Itcan be used in estimating thermal-expansion relief when usedin conjunction with the temperature at maximum dilation.3.1.2 temperature

7、at maximum dilationin addition to es-timating thermal-expansion relief, it can be used to rankproducts in terms of relative refractoriness. In general, thehigher the temperature at maximum dilation, the more refrac-tory the product and the better it is able to resist deformation atelevated temperatu

8、res.3.1.3 20 to 50 h creepthe percent deformation between the20 and 50 h can be used to rank products in terms of relativeload bearing capacity at a particular temperature. Relativerankings of various products may differ at different tempera-tures.4. Summary of Test Method4.1 Test specimens sawed fr

9、om samples of refractory brickor from prefabricated samples of monolithic refractories areplaced in a furnace and subjected to a prescribed compressivestress. Sensors are positioned for continuously measuring thelinear change of the specimens parallel to the direction of thecompressive stress. The t

10、emperature and linear change of thespecimens are continuously recorded while heating the furnaceat a controlled rate for thermal expansion under load testing.The time and linear change of the specimens are also continu-ously recorded while at soak temperature for 20 to 50 h ofcreep testing.4.2 The u

11、ser should be aware that other mechanisms,besides those related to creep, may be activated. This isespecially true as temperatures approach 1650C. When othermaterial responses are activated, such as corrosion, oxidation,sintering, etc., strong caution should be exercised when inter-preting and ident

12、ifying creep mechanisms.4.3 Since materials tend to exhibit faster creep rates duringthe initial stage of deformation, the user should be cautionedwhen extrapolating measured creep rates beyond the normal50 h test time. The material must be in the secondary creepstage in order to extrapolate to long

13、er times.5. Significance and Use5.1 The thermal expansion under load and the 20 to 50 hcreep properties of a refractory are useful in characterizing theload bearing capacity of a refractory that is uniformly heated.Directly applicable examples are blast furnace stoves and glassfurnace checkers.1This

14、 test method is under the jurisdiction of ASTM Committee C08 onRefractories and is the direct responsibility of Subcommittee C08.01 on Strength.Current edition approved March 1, 2015. Published May 2015. Originallyapproved in 1976. Last previous edition approved in 2010 as C832 00 (2010).DOI: 10.152

15、0/C0832-00R15.2For 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.Copyright ASTM International, 100 Barr Harbor D

16、rive, PO Box C700, West Conshohocken, PA 19428-2959. United States16. Interferences6.1 Chemical Interactions with Test EnvironmentThe testenvironment (vacuum, inert gas, ambient air, etc.), includingmoisture content (percent relative humidity), may have astrong influence on both creep strain rate an

17、d creep rupture life.In particular, refractories susceptible to slow crack growth oroxidation will be strongly influenced by the test environment.Testing should be conducted in environments that are eitherrepresentative of service conditions or inert to the refractoriesbeing tested depending on the

18、performance being evaluated.6.2 Specimen Surface PreparationSurface preparation ofspecimens can introduce machining flaws that may affect thecreep strain rate and creep rupture life. Machining damageimposed during specimen preparation will most likely result inpremature failure of the specimen, but

19、may also introduceflaws that can grow by slow crack growth. Surface preparationcan also lead to residual stresses, which can be released duringthe test.6.3 Specimen/Extensometer Chemical InteractionsIf thestrain measurement technique relies on physical contact be-tween the extensometer components (c

20、ontacting probes oroptical method flags) and the specimen, then the flag attach-ment methods and extensometer contact materials must bechosen with care to ensure that no adverse chemical reactionsoccur during testing. This should not be a problem if the probeor specimen materials are mutually chemic

21、ally inert. The usershould also be aware that impurities or second phases in theprobes and flags or specimens may be mutually chemicallyreactive and could influence the results.6.4 Temperature VariationsCreep strain is related to tem-perature through an exponential function. Thus, fluctuations intes

22、t temperature or changes in temperature profile along thelength of the specimen can cause fluctuations in strain mea-surements or changes in creep rate (see 7.1 and 7.2).7. Apparatus7.1 Electrically Heated Furnace, with a setting space suffi-cient to contain one or more specimens of the size specifi

23、ed inSection 8. The specimens should be equally heated on at leasttwo opposite sides, and the temperature difference betweenspecimens in a multiple-position furnace and between the topand bottom ends of single specimens should be no more than18F (10C). See Figs. 1-5 for sketches of five typical furn

24、acearrangements.7.2 Temperature Controllers, that control heating at a rate of100 6 9F/h (55 6 5C/h) over the temperature range from500 to 3000F (260 to 1650C) and can control soak tempera-tures within 69F (65C).7.3 Air Atmosphere, unless otherwise specified. If pitch orcarbonaceous-bonded materials

25、 are tested, specify the atmo-sphere used when reporting results.7.4 Linear Measuring Device, that records the difference inlength dimension of each specimen parallel to the direction ofstress and yields the desired precision and reproducibility.7.5 Recorders, that display linear change readings to6

26、0.0005 in. (0.013 mm).7.6 Loading Devices, that apply at least 100 psi (689 kPa)compressive stress within 61%, on a 112 by 112-in. (38 by38-mm) cross section.8. Specimen Preparation8.1 Cut or form specimens nominally 112 by 112 by 412 in.(38 by 38 by 114 mm) (Note 1) with the 412-in. dimensionFIG. 1

27、 Specimen Furnace ArrangementC832 00 (2015)2perpendicular to the pressing direction of a brick, the rammingdirection of a plastic, or the position of the vibrator used informing a castable. The 412-in. dimension may be parallel tothe length or width of the original shape.NOTE 1Specimens of different

28、 geometry (for example, cylindrical)may be used upon agreement between the parties concerned.8.2 Grind or sand both 112 by 112-in. (38 by 38-mm)surfaces so that they are nominally plane and perpendicular tothe length dimension. The parallelness tolerance on the loadingsurfaces of the specimen is rec

29、ommended to be within 0.001 in.(0.03 mm). Only the 112 by 112-in. (38 by 38-mm) and one 112by 412-in. (38 by 114-mm) surfaces may be original.8.3 Measure all dimensions to the nearest 0.001 in. (0.03mm) as follows:8.3.1 LengthAverage five measurements which includefour taken at14 in. (6 mm) on the d

30、iagonal from each cornerand one at the center of the faces.8.3.2 Width and DepthAverage three measurements whichinclude one taken at the center of the faces and two from thequarter points.8.3.3 Calculate the cross-sectional area of each specimenand use to determine the precise loading per specimen.9

31、. Calibration9.1 Calibrate each loading and measuring position sepa-rately. Follow the procedure given in Section 10 and determinethe “machine output” curves for each position using a speci-men of known thermal expansion. Calibration shall be done oneach new furnace and after replacement of any part

32、s of themeasuring or loading devices. Fused magnesium oxide (MgO)or isostatically pressed and fired MgO of 99 % minimum purityand 3.18 g/cm3minimum bulk density is recommended forstandardization. Volume stable 90 % plus aluminum oxide(Al2O3), fused silica (SiO2), or sapphire may also be used ifrelia

33、ble thermal expansion data are available. Make these runswith the loading mechanism blocked so that the specimen isessentially under zero stress.9.2 Make a minimum of three runs and record the measure-ments of linear change continuously with a computer/dataacquisition system or on a strip chart or X

34、-Y recorder or, ifdone manually, at 100F (55C) intervals up to 2000F(1095C) and 50F (28C) intervals above 2000F whileheating in accordance with 10.5. Reposition the specimen aftereach run to ensure that all random errors due to handling arerepeated each time. To ensure that the error for these runs

35、is nogreater than 60.05 % expansion at a probability level of 0.95,FIG. 2 Specimen Furnace ArrangementFIG. 3 Specimen Furnace ArrangementC832 00 (2015)3the standard deviation of the machine output cannot exceed0.02 percentage points.9.3 If MgO is chosen as the calibration standard, use theexpansion

36、data listed for MgO in Table 1.9.4 Obtain correction factors at the selected temperaturelevels from the algebraic difference between the averagemachine output in percent and the applicable true-expansionpercentage for the calibration standard. The algebraic sum ofthe correction factors and the machi

37、ne output of an unknownyields the expansion data in percent for the unknown.10. Procedure10.1 After leveling the hearth setters, place each specimenin the furnace with its longitudinal axis in alignment with thecenterline of the loading device. To protect the bottom of theload plunger, place a14-in.

38、 (6-mm) thick slab of alumina orsilicon carbide on top of the specimen. A slab works best if itis larger than the specimen, such as one that is approximatelyequal in length and width to the cross section of the plunger. Ifchemical reaction between specimen and furnace loading partsis expected, use a

39、 piece of 1-mil (25.4-m) thick platinum foilbetween the top and bottom of the specimen and the furnaceparts (Note 2). Do not use setting powder. The top of eachspecimen shall be level and parallel to the bottom setter.NOTE 2As testing temperatures approach 1650C, spacers of Al2O3,SiC, or Pt may not

40、be suitable due to chemical reaction with the specimenor creep of the spacer. Under these conditions, the measured dilation maybe significantly affected.10.2 Position linear measuring devices and check for free-dom of movement of sensor rods, dials, plungers, linearlyvariable differential transforme

41、rs (LVDTs), and operation ofrecording equipment.10.3 Apply loads on each specimen in the amount necessaryto provide the desired stress as determined by the specimencross-sectional area. The stress level used must accompany testresults. Use a stress of 25 psi (172 kPa) unless otherwisespecified. Stre

42、ss levels other than 25 psi (172 kPa) may be usedupon agreement between the interested parties.10.4 Use a calibrated thermocouple, preferably connected toa program controller, for measuring and controlling furnacetemperature. For accuracy in measuring specimen temperature,it is recommended that a gr

43、ounded, insulated, and calibratedthermocouple be placed so that the hot junction is within12 in.(6 mm) of the midpoint of every specimen (Note 3).NOTE 3Control of the temperature is essential for accurate results. Itis recommended that access ports be provided to periodically check thetemperature of

44、 each specimen with a calibrated thermocouple to ensurethat the desired temperature is obtained throughout the test.10.5 Heating control may be manual, but an electricallydriven program controller is preferred. Heat the furnace at arate of 1006 9F/h (55 6 5C/h) to the desired soak tempera-ture.10.6

45、For thermal expansion under load testing, continuouslyrecord the measurements of linear change with a computer/dataacquisition system or on a strip chart or X-Y recorder, orFIG. 4 Specimen Furnace ArrangementC832 00 (2015)4manually at intervals of 100F (55C) during heating. Attemperatures above 2000

46、F (1095C), take readings at 50F(28C) intervals.10.7 Continue heating until one of the following occurs:10.7.1 Linear thermal expansion ceases, and a maximumdilation level is identifiable, and 20 to 50 h creep testing is notdesired, or10.7.2 The specimen fails.10.8 For 20 to 50-h creep testing, hold

47、the specimen at thedesired soak temperature for 50 h. Continuously record themeasurement of linear change with a computer/data acquisitionsystem or on a strip chart or X-Y recorder, or manually atintervals of 5 h.10.9 Convert linear measurements to percent and record tothe nearest 0.001 %. Test at l

48、east two specimens. Each speci-men is considered a test result and replicates must be tested inthe same furnace.11. Report11.1 For the thermal expansion under load test, report theaverage and standard deviation for the temperature and linearchange at the maximum level of expansion where the creep ra

49、teequals the expansion rate. This point is called the maximumdilation point. Report temperature to the nearest 9F (5C) andexpansion to the nearest 0.001 %. Base results on at least twospecimens.11.2 For the 20 to 50 h creep test, report the average andstandard deviation for the creep between 20 and 50 h. Baseresults on at least two specimens.12. Precision and Bias12.1 Interlaboratory DataAn interlaboratory round robinwas conducted in 1983 in which four laboratories each testedtwo specimens from five different types of refr