ASTM D6450-2012e1 4775 Standard Test Method for Flash Point by Continuously Closed Cup &40 CCCFP&41 Tester《采用连续闭杯试验仪测定闪点40 CCCFP41的标准试验方法》.pdf

《ASTM D6450-2012e1 4775 Standard Test Method for Flash Point by Continuously Closed Cup &40 CCCFP&41 Tester《采用连续闭杯试验仪测定闪点40 CCCFP41的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D6450-2012e1 4775 Standard Test Method for Flash Point by Continuously Closed Cup &40 CCCFP&41 Tester《采用连续闭杯试验仪测定闪点40 CCCFP41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: D6450 121Standard Test Method forFlash Point by Continuously Closed Cup (CCCFP) Tester1This standard is issued under the fixed designation D6450; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revisio

2、n. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1NOTEEditorially removed sole source of supply footnote from 6.1 in February 2014.1. Scope*1.1 This flash point test method is a dynamic metho

3、d anddepends on definite rates of temperature increase. It is one ofthe many flash point test methods available, and every flashpoint test method, including this one, is an empirical method.NOTE 1Flash point values are not a constant physical-chemicalproperty of materials tested. They are a function

4、 of the apparatus design,the condition of the apparatus used, and the operational procedure carriedout. Flash point can therefore only be defined in terms of a standard testmethod, and no general valid correlation can be guaranteed betweenresults obtained by different test methods or with test appar

5、atus differentfrom that specified.1.2 This test method covers the determination of the flashpoint of fuel oils, lube oils, solvents, and other liquids by acontinuously closed cup tester. The measurement is made on atest specimen of 1 mL.1.3 This test method utilizes a closed but unsealed cup withair

6、 injected into the test chamber.1.4 This test method is suitable for testing samples with aflash point from 10 to 250C.NOTE 2Flash point determinations below 10C and above 250C canbe performed; however, the precision has not been determined below andabove these temperatures.1.5 If the users specific

7、ation requires a defined flash pointmethod other than this test method, neither this test method norany other method should be substituted for the prescribedmethod without obtaining comparative data and an agreementfrom the specifier.1.6 The values stated in SI units are to be regarded asstandard. N

8、o other units of measurement are included in thisstandard. Temperatures are in degrees Celsius, and pressure isin kilo-pascals.1.7 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 a

9、ppro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use. Specific warningstatements appear throughout the standard.2. Referenced Documents2.1 ASTM Standards:2D4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsD4177 Practice fo

10、r Automatic Sampling of Petroleum andPetroleum ProductsD6299 Practice for Applying Statistical Quality Assuranceand Control Charting Techniques to Evaluate AnalyticalMeasurement System PerformanceD6300 Practice for Determination of Precision and BiasData for Use in Test Methods for Petroleum Product

11、s andLubricantsE300 Practice for Sampling Industrial Chemicals2.2 ISO Standards:3ISO Guide 34 Quality Systems Guidelines for the Produc-tion of Reference MaterialsISO Guide 35 Certifications of Reference Material Generaland Statistical Principles3. Terminology3.1 Definitions:3.1.1 dynamic, adjthe co

12、ndition in which the vapor abovethe test specimen and the test specimen are not in temperatureequilibrium at the time at which the ignition source is applied.3.1.2 flash point, nthe lowest temperature corrected to apressure of 101.3 kPa at which application of an ignitionsource causes the vapors of

13、a specimen of the sample to ignitemomentarily under specified conditions of the test.3.1.2.1 DiscussionFor the purpose of this test method, thetest specimen is deemed to have flashed when the hot flame of1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products, Liquid F

14、uels, and Lubricants and is the direct responsibility ofSubcommittee D02.08 on Volatility.Current edition approved Dec. 1, 2012. Published March 2013. Originallyapproved in 1999. Last previous edition approved in 2010 as D645005 (2010).DOI: 10.1520/D6450-12.2For referenced ASTM standards, visit the

15、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.3Available from American National Standards Institute (ANSI), 25 W. 43rd St.,4th Floor, New York, NY 10

16、036, http:/www.ansi.org.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States1the ignited vapor causes an instantaneous pressure increase ofat least 20 kPa inside the closed m

17、easuring chamber.4. Summary of Test Method4.1 The lid of the test chamber is regulated to a temperatureat least 18C below the expected flash point.A1 6 0.1 mL testspecimen of a sample is introduced into the sample cup,ensuring that both specimen and cup are at a temperature atleast 18C below the exp

18、ected flash point, cooling if necessary.The cup is then raised and pressed onto the lid of specifieddimensions to form the continuously closed but unsealed testchamber with an overall volume of 4.0 6 0.2 mL.4.2 After closing the test chamber, the temperatures of thetest specimen and the regulated li

19、d are allowed to equilibrate towithin 1C. Then the lid is heated at a prescribed, constant rate.For the flash tests, an arc of defined energy is discharged insidethe test chamber at regular intervals. After each ignition, 1.5 60.5 mL of air is introduced into the test chamber to provide thenecessary

20、 oxygen for the next flash test. The pressure inside thecontinuously closed but unsealed test chamber remains atambient barometric pressure, except for the short time duringthe air introduction and except at a flash point.4.3 After each arc, the instantaneous pressure increaseabove the ambient barom

21、etric pressure inside the test chamberis monitored. When the pressure increase exceeds a definedthreshold, the temperature at that point is recorded as theuncorrected flash point.5. Significance and Use5.1 The flash point temperature is one measure of thetendency of the test specimen to form a flamm

22、able mixturewith air under controlled laboratory conditions. It is only oneof a number of properties that must be considered in assessingthe overall flammability hazard of a material.5.2 Flash point is used in shipping and safety regulations todefine flammable and combustible materials and classify

23、them.This definition may vary from regulation to regulation. Consultthe particular regulation involved for precise definitions ofthese classifications.5.3 This test method can be used to measure and describethe properties of materials in response to heat and an ignitionsource under controlled labora

24、tory conditions and shall not beused to describe or appraise the fire hazard or fire risk ofmaterials under actual fire conditions. However, results of thistest method may be used as elements of a fire risk assessment,which takes into account all of the factors that are pertinent toan assessment of

25、the fire hazard of a particular end use.5.4 Flash point can also indicate the possible presence ofhighly volatile and flammable materials in a relatively non-volatile or nonflammable material, such as the contaminationof lubricating oils by small amounts of diesel fuel or gasoline.6. Apparatus6.1 Fl

26、ash Point Apparatus, Continuously Closed CupOperationThe type of apparatus suitable for use in this testmethod employs a lid of solid brass, the temperature of whichis controlled electrically. Two temperature sensors for thespecimen and the lid temperatures, respectively, two electri-cally insulated

27、 pins for a high voltage arc, and a connectingtube for the pressure monitoring and the air introduction areincorporated in the lid. Associated equipment for electricallycontrolling the chamber temperature is used, and a digitalreadout of the specimen temperature is provided. The appara-tus and its c

28、ritical elements are shown in Fig. A1.1 and Fig.A1.2.6.1.1 Test ChamberThe test chamber is formed by thesample cup and the temperature controlled lid and shall have anoverall volume of 4 6 0.2 mL. A metal to metal contactbetween the lid and the sample cup shall provide good heatcontact but allow amb

29、ient barometric pressure to be maintainedinside the test chamber during the test. Critical dimensions areshown in Fig. A1.2. The pressure inside the measuring cham-ber during the temperature increase is monitored. A seal that istoo tight results in a pressure increase above ambient due to thetempera

30、ture and the vapor pressure of the sample. A poor heatcontact results in a bigger temperature difference between thesample and the heated lid.6.1.2 Sample CupThe sample cup shall be made ofnickel-plated aluminum or other material with similar heatconductivity. It shall have an overall volume of 4 mL

31、 and shallbe capable of containing 1 6 0.1 mL of sample. The criticaldimensions and requirements are shown in Fig. A1.2.6.1.3 Specimen Temperature SensorThe specimen tem-perature sensor (Fig. A1.1: Ts) shall be a thermocouple(NiCr-Ni or similar) in stainless steel of 1-mm diameter with aresponse tim

32、e of t(90)=3s.Itshall be immersed to a depth ofat least 2 mm into the specimen. It shall have a resolution of0.1C and a minimum accuracy of 6 0.2C, preferably with adigital readout.6.1.4 Magnetic StirringThe apparatus shall have provi-sions for stirring the sample. A rotating magnet outside thesampl

33、e cup shall drive a small stirring magnet, which isinserted into the sample cup after sample introduction. Thestirring magnet shall have a diameter of 3 6 0.2 mm and alength of 12 6 1 mm. The rotation speed of the driving magnetshall be between 250 and 270 rev/min.6.1.5 Air IntroductionThe apparatus

34、 shall have provisionsfor introduction of 1.5 6 0.5 mL of air immediately after eachflash test. The air shall be introduced by a short air pulse froma small membrane compressor by means of a T-inlet in theconnecting tube to the pressure transducer.6.1.6 Electrical heating and thermoelectric cooling

35、of the lid(Fig. A1.1: PE) shall be used to regulate the temperature of thetest chamber for the duration of the test. The temperatureregulation shall have a minimum accuracy of 6 0.2C.6.1.7 A high voltage electric arc shall be used for theignition of the flammable vapor. The energy of the arc shall b

36、e3 6 0.5 mJ (3 6 0.5 Ws) per arc, and the energy shall beapplied within 43 6 3 ms. (WarningBecause samplescontaining low flash material or having a flash point below thepreset initial temperature can oversaturate the vapor inside thechamber and hence prohibit the detection of a flash point in thecho

37、sen range, the design of the apparatus should incorporatestep-wise ignitions in steps of 10C, following the closing ofD6450 1212the measuring chamber and before the sample reaches theinitial temperature of the test.)6.1.8 The pressure transducer for the flash point detectionshall be connected to the

38、 connecting tube in the lid and shallhave a minimum operational range from 80 to 177 kPa with aminimum resolution of 0.1 kPa and a minimum accuracy of60.5 kPa. It shall be capable of detecting an instantaneouspressure increase above barometric pressure of a minimum of20 kPa within 100 ms.NOTE 3The m

39、onitoring of the instantaneous pressure increase abovebarometric pressure is one of several methods used to determine a flashinside the test chamber. A pressure increase of 20 kPa corresponds to aflame volume of approximately 1.5 mL.NOTE 4An automatic barometric correction, which is performed inacco

40、rdance with the procedure described in 12.1, can be installed in thetester. The absolute pressure reading of the pressure transducer describedin 6.1.8 may be used for the correction.6.1.9 The introduction of a test portion of 1.0 6 0.1 mLshall be accomplished by the use of a pipette or syringe of th

41、erequired accuracy.7. Reagents and Materials7.1 Purity of ReagentsUse only chemicals of purity re-quested in Table X1.1. Unless otherwise indicated, it isintended that all reagents conform to the specifications of theCommittee on Analytical Reagents of the American ChemicalSociety where such specifi

42、cations are available.4Other gradesmay be used, provided it is first ascertained that the reagent isof sufficient purity to permit its use without lessening theaccuracy of the determination.7.1.1 Anisole(WarningFlammable and a health hazard.Dispose of solvents and waste material in accordance withlo

43、cal regulations.)7.1.2 Dodecane(WarningFlammable and a health haz-ard. Dispose of solvents and waste material in accordance withlocal regulations.)7.2 Cleaning SolventsUse only noncorrosive solvents ca-pable of cleaning the sample cup and the lid. Two commonlyused solvents are toluene and acetone. (

44、WarningFlammableand a health hazard. Dispose of solvents and waste material inaccordance with local regulations.)8. Sampling8.1 Obtain at least a 50 mL sample from a bulk test site inaccordance and instruction given in Practice D4057, D4177,orE300. Store the sample in a clean, tightly sealed contain

45、er at alow temperature.8.2 Do not store samples for an extended period of time ingas permeable containers, such as plastic, because volatilematerial may diffuse through the walls of the container.Discard samples in leaky containers and obtain new samples.8.3 Erroneously high flash points can be obta

46、ined whenprecautions are not taken to avoid loss of volatile material. Donot open containers unnecessarily. Do not make a transferunless the sample temperature is at least 18C below theexpected flash point. When possible, perform the flash point asthe first test.8.4 Samples of very viscous materials

47、 may be warmed untilthey are reasonably fluid before they are tested. However, donot heat the unsealed sample above a temperature of 18Cbelow its expected flash point.8.5 Samples containing dissolved or free water may bedehydrated with calcium chloride or by filtering through aqualitative filter pap

48、er or a loose plug of dry absorbent cotton.Warming the sample is permitted, but do not heat the sampleabove a temperature of 18C below its expected flash point.(WarningBecause samples containing volatile material willlose volatiles and then yield incorrectly high flash points, thetreatment described

49、 in 8.4 and 8.5 is not suitable for suchsamples.)9. Quality Control Checks9.1 Verify the performance of the instrument at least onceper year by determining the flash point of a certified referencematerial (CRM) such as those listed in Appendix X1, which isreasonably close to the expected temperature range of thesamples to be tested. The material shall be tested in accordancewith Section 11 of this test method, and the observed flashpoint obtained in 11.11 shall be corrected for barometricpressure as described in Section 12. The flash point s