ASTM D92-2012a Standard Test Method for Flash and Fire Points by Cleveland Open Cup Tester《使用克氏开口杯闪点测定器测定闪点或燃点的标准试验方法》.pdf

《ASTM D92-2012a Standard Test Method for Flash and Fire Points by Cleveland Open Cup Tester《使用克氏开口杯闪点测定器测定闪点或燃点的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D92-2012a Standard Test Method for Flash and Fire Points by Cleveland Open Cup Tester《使用克氏开口杯闪点测定器测定闪点或燃点的标准试验方法》.pdf（10页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D92 12a American Association StateHighway and Transportation Officials StandardAASHTO No.: T48DIN 51 376Standard Test Method forFlash and Fire Points by Cleveland Open Cup Tester1This standard is issued under the fixed designation D92; the number immediately following the designation in

2、dicates the year of originaladoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A superscriptepsilon () indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies

3、of the Department of Defense.INTRODUCTIONThis flash point and fire point test method is a dynamic method and depends on definite rates oftemperature increases to control the precision of the test method. Its primary use is for viscousmaterials having flash point of 79C (175F) and above. It is also u

4、sed to determine fire point, whichis a temperature above the flash point, at which the test specimen will support combustion for aminimum of 5 s. Do not confuse this test method with Test Method D4206, which is a sustainedburning test, open cup type, at a specific temperature of 49C (120F).Flash poi

5、nt values are a function of the apparatus design, the condition of the apparatus used, andthe operational procedure carried out. Flash point can therefore only be defined in terms of a standardtest method, and no general valid correlation can be guaranteed between results obtained by differenttest m

6、ethods, or with test apparatus different from that specified.1. Scope*1.1 This test method describes the determination of the flashpoint and fire point of petroleum products by a manualCleveland open cup apparatus or an automated Cleveland opencup apparatus.NOTE 1The precisions for fire point were n

7、ot determined in thecurrent interlaboratory program. Fire point is a parameter that is notcommonly specified, although in some cases, knowledge of this flamma-bility temperature may be desired.1.2 This test method is applicable to all petroleum productswith flash points above 79C (175F) and below 40

8、0C(752F) except fuel oils.NOTE 2This test method may occasionally be specified for thedetermination of the fire point of a fuel oil. For the determination of theflash points of fuel oils, use Test Method D93. Test Method D93 shouldalso be used when it is desired to determine the possible presence of

9、 small,but significant, concentrations of lower flash point substances that mayescape detection by Test Method D92. Test Method D1310 can beemployed if the flash point is known to be below 79C (175F).1.3 The values stated in SI units are to be regarded as thestandard. The values given in parentheses

10、 are for informationonly.1.4 WARNINGMercury has been designated by manyregulatory agencies as a hazardous material that can causecentral nervous system, kidney and liver damage. Mercury, orits vapor, may be hazardous to health and corrosive tomaterials. Caution should be taken when handling mercury

11、andmercury containing products. See the applicable product Ma-terial Safety Data Sheet (MSDS) for details and EPAswebsitehttp:/www.epa.gov/mercury/faq.htmfor addi-tional information. Users should be aware that selling mercuryand/or mercury containing products into your state or countrymay be prohibi

12、ted by law.1.5 This standard 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. For

13、 specificwarning statements, see 6.4, 7.1, 11.1.3, and 11.2.4.1This test method is under the joint jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.08 on Volatility. In the IP, this test method is under the jurisdiction of the

14、Standardization Committee. This test method was adopted as a joint ASTM-IPstandard in 1965.Current edition approved November 2012. Published December 2012. Originallyapproved in 1921. Last previous edition approved in 2012 as D9212. DOI:10.1520/D0092-12A.*A Summary of Changes section appears at the

15、end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States12. Referenced Documents2.1 ASTM Standards:2D93 Test Methods for Flash Point by Pensky-MartensClosed Cup TesterD140 Practice for Sampling Bituminous MaterialsD1310 Tes

16、t Method for Flash Point and Fire Point of Liquidsby Tag Open-Cup ApparatusD4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsD4177 Practice for Automatic Sampling of Petroleum andPetroleum ProductsD4206 Test Method for Sustained Burning of Liquid Mix-tures Using the Small Scale Op

17、en-Cup ApparatusE1 Specification for ASTM Liquid-in-Glass ThermometersE300 Practice for Sampling Industrial Chemicals2.2 Energy Institute Standard:3Specifications for IP Standard Thermometers2.3 ISO Standards:4Guide 34 Quality Systems Guidelines for the Production ofReference MaterialsGuide 35 Certi

18、fication of Reference MaterialGeneral andStatistical Principles3. Terminology3.1 Definitions:3.1.1 dynamic, adjin petroleum products, the conditionwhere the vapor above the test specimen and the test specimenare not in temperature equilibrium at the time that the ignitionsource is applied.3.1.1.1 Di

19、scussionThis is primarily caused by the heatingof the test specimen at the constant prescribed rate with thevapor temperature lagging behind the test specimen tempera-ture.3.1.2 fire point, nin petroleum products, the lowest tem-perature corrected to a barometric pressure of 101.3 kPa (760mm Hg), at

20、 which application of an ignition source causes thevapors of a test specimen of the sample to ignite and sustainburning for a minimum of 5 s under specified conditions oftest.3.1.3 flash point, n in petroleum products, the lowesttemperature corrected to a barometric pressure of 101.3 kPa(760 mm Hg),

21、 at which application of an ignition source causesthe vapors of a specimen of the sample to ignite under specifiedconditions of test.4. Summary of Test Method4.1 Approximately 70 mL of test specimen is filled into atest cup. The temperature of the test specimen is increasedrapidly at first and then

22、at a slower constant rate as the flashpoint is approached.At specified intervals a test flame is passedacross the cup. The flash point is the lowest liquid temperatureat which application of the test flame causes the vapors of thetest specimen of the sample to ignite. To determine the firepoint, the

23、 test is continued until the application of the test flamecauses the test specimen to ignite and sustain burning for aminimum of 5 s.5. Significance and Use5.1 The flash point is one measure of the tendency of the testspecimen to form a flammable mixture with air under con-trolled laboratory conditi

24、ons. It is only one of a number ofproperties that should be considered in assessing the overallflammability hazard of a material.5.2 Flash point is used in shipping and safety regulations todefine flammable and combustible materials. Consult theparticular regulation involved for precise definitions

25、of theseclassifications.5.3 Flash point can indicate the possible presence of highlyvolatile and flammable materials in a relatively nonvolatile ornonflammable material. For example, an abnormally low flashpoint on a test specimen of engine oil can indicate gasolinecontamination.5.4 This test method

26、 shall be used to measure and describethe properties of materials, products, or assemblies in responseto heat and a test flame under controlled laboratory conditionsand shall not be used to describe or appraise the fire hazard orfire risk of materials, products, or assemblies under actual firecondit

27、ions. However, results of this test method may be used aselements of a fire risk assessment that takes into account all ofthe factors that are pertinent to an assessment of the fire hazardof a particular end use.5.5 The fire point is one measure of the tendency of the testspecimen to support combust

28、ion.6. Apparatus6.1 Cleveland Open Cup Apparatus (manual)This appa-ratus consists of the test cup, heating plate, test flameapplicator, heater, and supports described in detail in the AnnexA1. The assembled manual apparatus, heating plate, and cupare illustrated in Figs. 1-3, respectively. Dimension

29、s are listedwith the figures.6.2 Cleveland Open Cup Apparatus (automated)This ap-paratus is an automated flash point instrument that shallperform the test in accordance with Section 11 Procedure. Theapparatus shall use the test cup with the dimensions asdescribed in Annex A1 and the application of t

30、he test flameshall be as described in Annex A1.6.3 Temperature Measuring DeviceAthermometer havingthe range as shown below and conforming to the requirementsprescribed in Specification E1 or in the Specifications for IPStandard Thermometers, or an electronic temperature measur-ing device, such as a

31、resistance thermometer or thermocouple.The device shall exhibit the same temperature response as themercury thermometers.Thermometer NumberTemperature Range ASTM IP6 to +400C 11C 28C20 to 760F 11F2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at

32、 serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Available from Energy Institute, 61 New Cavendish St., London, WIG 7AR,U.K., http:/www.energyinst.org.uk.4Available from American National Standards Institute (ANSI

33、), 25 W. 43rd St.,4th Floor, New York, NY 10036.D92 12a26.4 Test FlameNatural gas (methane) flame and bottledgas (butane, propane) flame have been found acceptable for useFIG. 1 Cleveland Open Cup Apparatusmillimetres inchesmin max min maxA 6 7 0.236 0.276B 0.5 1.0 0.020 0.039C 6 7 0.236 0.276DDiame

34、ter 55 56 2.165 2.205EDiameter 69.5 70.5 2.736 2.776FDiameter 146 159 5.748 6.260FIG. 2 Heating PlateFIG. 3 Cleveland Open CupD92 12a3as the ignition source. The gas flame device is described indetail in Annex A1.(Warning Gas pressure supplied to theapparatus must not be allowed to exceed 3 kPa (12

35、in.) of waterpressure.)7. Reagents and Materials7.1 Cleaning SolventsUse suitable technical grade solventcapable of cleaning out the test specimen from the test cup anddrying the test cup. Some commonly used solvents are tolueneand acetone. (WarningToluene, acetone, and many solventsare flammable. H

36、ealth hazard. Dispose of solvents and wastematerial in accordance with local regulations.)8. Sampling8.1 Obtain a sample in accordance with the instructionsgiven in Practices D140, D4057, D4177 or E300.8.2 At least 70 mL of sample is required for each test. Referto Practice D4057.8.3 Erroneously hig

37、h flash points may be obtained if pre-cautions are not taken to avoid the loss of volatile material. Donot open containers unnecessarily; this will prevent loss ofvolatile material and possible introduction of moisture. Do notmake a transfer of the sample unless the sample temperature isat least 56C

38、 (100F) below the expected flash point. Whenpossible, flash point should be the first test performed on asample and the sample should be stored at low temperature.NOTE 3Typical sample storage temperature is normal room tempera-ture or lower.8.4 Do not store samples in gas-permeable containers sincev

39、olatile material may diffuse through the walls of the enclo-sure. Samples in leaky containers are suspect and not a sourceof valid results.8.5 Light hydrocarbons may be present in the form of gases,such as propane or butane, and may not be detected by testingbecause of losses during sampling and fil

40、ling of the test cup.This is especially evident on heavy residuums or asphalts fromsolvent extraction processes.8.6 Samples of very viscous materials can be warmed untilthey are reasonably fluid before they are tested. However, nosample shall be heated more than is absolutely necessary. Itshall neve

41、r be heated above a temperature of 56C (100F)below its expected flash point. When the sample has beenheated above this temperature, allow the sample to cool until itis at least 56C (100F) below the expected flash point beforetransferring.NOTE 4Typically, the sample containers for these types of samp

42、leswill remain closed during the warming process.8.7 Samples containing dissolved or free water can bedehydrated with calcium chloride or by filtering through aqualitative filter paper or a loose plug of dry absorbent cotton.Samples of very viscous materials can be warmed until they arereasonably fl

43、uid before they are filtered, but they shall not beheated for prolonged periods or above a temperature of 56C(100F) below its expected flash point.NOTE 5If the sample is suspected of containing volatile contaminants,the treatment described in 8.6 and 8.7 should be omitted.9. Preparation of Apparatus

44、9.1 Support the manual or automated apparatus on a levelsteady surface, such as a table.9.2 Tests are to be performed in a draft-free room orcompartment. Tests made in a laboratory hood or in anylocation where drafts occur are not to be relied upon.NOTE 6A draft shield is recommended to prevent draf

45、ts fromdisturbing the vapors above the test cup. This shield should cover at leastthree sides of the test cup vicinity. Some apparatus may already include abuilt-in draft shield.NOTE 7With some samples whose vapors or products of pyrolysis areobjectionable, it is permissible to place the apparatus a

46、long with a shieldinto a hood, the draft of which is adjusted so that the vapors may bewithdrawn without causing air currents over the test cup during the final56C (100F) rise in temperature prior to the flash point.9.3 Wash the test cup with the cleaning solvent to removeany test specimen or traces

47、 of gum or residue remaining froma previous test. If any deposits of carbon are present, theyshould be removed with a material such as a very fine grade ofsteel wool. Ensure that the test cup is completely clean and drybefore using again. If necessary, flush the test cup with coldwater and dry for a

48、 few minutes over an open flame or a hotplate to remove the last traces of solvent and water. Cool thetest cup to at least 56C (100F) below the expected flash pointbefore using.9.4 Support the temperature measuring device in a verticalposition with the bottom of the device located 6.4 6 0.1 mm(14 61

49、50 in.) up from the bottom of the inside of the test cupand located at a point halfway between the center and the sideof the test cup on a diameter perpendicular to the arc (or line)of the sweep of the test flame and on the side opposite to thetest flame applicator mounting position.NOTE 8The immersion line engraved on theASTM or IPthermometerwill be 2 6 0.1 mm (564 6150 in.) below the level of the rim of the cupwhen the thermometer is properly positioned.NOTE 9Some automated apparatus is capable of positioning thetemperatu