ASTM E918-1983(2005) Standard Practice for Determining Limits of Flammability of Chemicals at Elevated Temperature and Pressure《温度和压力升高时化学药品易燃极限的测定》.pdf

《ASTM E918-1983(2005) Standard Practice for Determining Limits of Flammability of Chemicals at Elevated Temperature and Pressure《温度和压力升高时化学药品易燃极限的测定》.pdf》由会员分享，可在线阅读，更多相关《ASTM E918-1983(2005) Standard Practice for Determining Limits of Flammability of Chemicals at Elevated Temperature and Pressure《温度和压力升高时化学药品易燃极限的测定》.pdf（5页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E 918 83 (Reapproved 2005)Standard Practice forDetermining Limits of Flammability of Chemicals at ElevatedTemperature and Pressure1This standard is issued under the fixed designation E 918; the number immediately following the designation indicates the year oforiginal adoption or, in th

2、e case of revision, the year of last revision. 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 practice covers the determination of the lower andupper concentration limits of

3、flammability of combustiblevapor-oxidant mixtures at temperatures up to 200C and initialpressures up to as much as 1.38 MPa (200 psia). This practiceis limited to mixtures which would have explosion pressuresless than 13.79 MPa (2000 psia).1.2 This practice should be used to measure and describethe

4、properties of materials, products, or assemblies in responseto heat and flame under controlled laboratory conditions andshould not be used to describe or appraise the fire hazard orfire risk of materials, products, or assemblies under actual fireconditions. However, results of this test may be used

5、aselements of a fire risk assessment which takes into account allof the factors which are pertinent to an assessment of the firehazard of a particular end use.1.3 This standard may involve hazardous materials, opera-tions, and equipment. This standard does not purport toaddress all of the safety pro

6、blems associated with its use. It isthe responsibility of the user of this standard to establishappropriate safety and health practices and determine theapplicability of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:E 681 Test Method for Limits of Flammability of Chem

7、i-cals22.2 Other Documents:Bulletin 503, Bureau of Mines, “Limits of Flammability ofGases and Vapors,” NTIS AD701575Bulletin 627, Bureau of Mines, “Flammability Characteris-tics of Combustible Gases and Vapors,” NTIS AD7015763. Terminology3.1 Definitions:3.1.1 lower limit of flammability or lower fl

8、ammable limit(LFL)the minimum concentration of a combustible sub-stance that is capable of propagating a flame through ahomogeneous mixture of the combustible and a gaseousoxidizer under the specified conditions of test.3.1.2 upper limit of flammability or upper flammable limit(UFL)the maximum conce

9、ntration of a combustible sub-stance that is capable of propagating a flame through ahomogeneous mixture of the combustible and a gaseousoxidizer under the specified conditions of test.3.2 Definitions of Terms Specific to This Standard:3.2.1 propagation of flames as used in this practice,acombustion

10、 reaction that produces at least a 7 % rise of theinitial absolute pressure,P2P11.07.NOTE 1This 7 % rise in pressure corresponds to 1 psia (0.007 MPa)per atmosphere of initial pressure.4. Summary of Practice4.1 A mixture of gaseous or vaporized fuel with a gaseousoxidizer is prepared in a steel or o

11、ther appropriate metal vesselat a controlled temperature and pressure. Proportions of thecomponents are determined by measurement of partial pres-sures during filling of the vessel. Ignition of the mixture isattempted with a fuse wire, and flammability is deduced fromthe pressure rise produced. Fuel

12、 concentration is varied be-tween trials until the limits of flammability have been deter-mined. Composition of the mixtures which fix the flammablelimits are confirmed by appropriate analysis.5. Significance and Use5.1 Knowledge of flammable limits at elevated temperaturesand pressures is needed fo

13、r safe and economical operation ofsome chemical processes. This information may be needed inorder to start up a reactor without passing through a flammable1This practice is under the jurisdiction of ASTM Committee E27 on HazardPotential of Chemicals and is the direct responsibility of Subcommittee E

14、 27.04 onFlammability and Ignition of Chemicals.Current edition approved Sept. 15, 2005. Published December 2005. Originallyapproved in 1983. Last previous edition approved in 1999 as E 918 83 (1999).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Servic

15、e at serviceastm.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.range, to operate the reactor safely and econo

16、mically, or tostore or ship the product safely.5.2 Limits of flammability data obtained in relatively cleanvessels must be carefully interpreted and may not always beapplicable to industrial conditions. Surface effects due tocarbon deposits and other materials can significantly affectlimits of flamm

17、ability, especially in the fuel-rich region. Referto Bulletin 503 and 627.6. Limitations6.1 This practice is not applicable to mixtures which un-dergo spontaneous reaction before ignition is attempted.6.2 Measured limits of flammability are influenced byflame-quenching effects of the test vessel wal

18、ls. The vesseldescribed in this practice is suitable for use with most mixturesat elevated temperatures and pressures. For certain amines,halogenated materials etc., which have large ignition-quenching distances, tests may need to be conducted in largerdiameter vessels.7. Apparatus7.1 Fig. 1 is a sc

19、hematic diagram of the apparatus; detailsand dimensions are presented in Annex A1. The apparatusconsists of a metal pressure vessel with a minimum volume of1 L and a minimum inside diameter of 76 mm (3 in.), aninsulated chamber equipped with a source of controlled-temperature inert gas, an ignition

20、device with appropriatepower supply, remotely controlled valves, pressure measuringequipment, and a venting system for handling overpressuring.8. Safety Precautions8.1 Adequate shielding must be provided to prevent injuryin the event of equipment rupture. The apparatus is set up sothat the operator

21、is isolated by a blast-proof wall from the testvessel while the vessel contains a charge of reactants, includingthe time while the vessel is being filled. The test apparatusshould be equipped with interlocks so that the ignition sourcecannot be activated unless the operator has taken necessarysteps

22、to protect personnel and equipment. Activation of theignition source should be possible only from a positionshielded from the test vessel.8.2 The test vessel shall be fitted with a rupture disk ventedoutside any enclosed area. Fuel may inadvertently be ventedinside the heated chamber or inside the e

23、nclosed area, so theFIG. 1 Schematic Diagram of Test ApparatusE 918 83 (2005)2heated chamber should be fitted with an inert gas purge and thearea should be adequately ventilated to prevent buildup of anexplosive mixture in the large space.8.3 Undesirably energetic explosions may be produced iftests

24、are made at high initial pressures with mixtures wellwithin the flammable range. Very strong oxidizers greatlyincrease explosion severity and also greatly increase thefuel-rich limit. To help in avoiding testing highly energeticmixtures, limits of flammability should first be determined atatmospheri

25、c pressure. These limits are covered in MethodE 681. With this knowledge, the operator should proceed incautious steps of initial pressure increase to work at higherpressures and temperatures.9. Preparation of Apparatus9.1 Clean and dry the test vessel and other gas-handlingequipment. Make sure that

26、 no oil, grease, or other combustibleis left inside the parts.9.2 Assemble the equipment as shown in Fig. 1. Purge thevessel with inert gas and then evacuate the system.9.3 Set the zero and gain on the pressure transducers so thattheir output represents true pressure after the test vessel is atthe w

27、orking temperature.METHOD ASAMPLE COMPONENTS WHICHHAVE ADEQUATE VAPOR PRESSURE AT ROOMTEMPERATURE10. Procedure10.1 Attach pressure regulators to the supply cylinders ofgases to be used in the tests. Connect the regulators to themanifold of remotely-controlled metering valves.10.2 Flush each line fro

28、m the supply cylinder to the meter-ing valve. Evacuate the test vessel and manifold. By use of theremotely controlled valves, add to the test vessel the compo-nent most appropriately added first; usually, this is the smallestcomponent. Close the ball valve next to the test vessel andevacuate or purg

29、e the manifold.10.3 Add the second component up to the desired pressure,as measured by the transducer. Repeat the clearing of themanifold and add components until the desired partial pressureof each component has been added to the test vessel. Obtainmixing of gas in the test vessel by adding the lar

30、gest compo-nent last and at high velocity.NOTE 2Both fast addition of the last component and restricting the tipof the dip tube are necessary to achieve homogeneity. One way to add gasat high velocity with low risk of overshooting is to make use of aquick-opening dump valve on the pneumatic actuator

31、 system for themetering valve. The last component should be added in less than 15 s.NOTE 3Where the vessel configuration will permit, an internal mixingdevice may be used.NOTE 4If the pressure and temperature do not hold steady after acomponent is added this may indicate reaction prior to ignition.

32、Reactionof a halogen will probably cause a pressure drop. Reaction of oxygen willprobably cause a pressure rise.10.4 Close the remotely controlled valve between the testvessel and the low-range pressure transducer in order to protectthis transducer from explosion pressure.10.5 Allow the test gas mix

33、ture to equilibrate to testconditions.10.6 Early in the test series, use an appropriate method suchas gas chromatography to confirm composition of gas mixturesmade ready for explosion test. Make any changes in techniquenecessary to ensure homogeneous mixture. These mixturesmay not have the compositi

34、on expected, due to nonideal gasbehavior. Errors will vary with the order of mixing, tempera-ture, pressure, and the particular materials.Also, the greater thedead volume in tubing etc., not involved in mixing with thecharge in the cylinder, the greater will be the difference fromexpected compositio

35、n. If the composition is wrong makeadjustments in partial pressure to get desired composition.10.7 Record the temperature and pressure of the test gas.10.8 Activate the pressure recording equipment.10.9 Attempt ignition of the gas mixture by applying 115 Vacross the fuse wire.10.10 Record the maximu

36、m pressure.10.11 Vent the test vessel through the exhaust valve. Purgethe vessel with inert gas from the manifold.10.12 Install another spark plug fitted with a fuse wire.NOTE 5By having the spark plug positioned in front of a socketwrench-sized hole in the wall of the heated chamber, the plug can b

37、echanged without appreciably cooling off the chamber. Use a deep socketwrench which fits the bushing, not the spark plug.10.13 Vary fuel concentration (percent of the total vaporpressure) as required to find the minimum concentration, L1,that gives flame propagation and the maximum concentration,L2,

38、 below L1, that does not give flame propagation. Flamepropagation by this method is defined as a pressure ratioP2P1of 1.07 or more. Record values for L1and L2measured bypressure during filling of the test vessel and by analysis of themixtures. Repeat the analysis and test on composition L2toconfirm

39、its non-flammability.10.14 Commence upper limit tests in the nonflammableregion at a concentration greater than the anticipated U2. (See10.16.) Fuel concentration at the upper limit may be substan-tially greater at elevated temperature and pressure than it is atatmospheric conditions.10.15 Remove an

40、y carbon deposits that may be left in thetest vessel after a fuel-rich explosion.NOTE 6These deposits are likely to affect subsequent results. Toremove the carbon insert through the spark plug hole an L-shaped piece of6.4-mm (14-in.) metal tubing attached by a flexible hose to an inert gassupply. Bl

41、ow inert gas vigorously around inside the test vessel until nomore carbon is displaced. Finish cleaning out the carbon by igniting, as ifit were the next sample, a fuel-lean mixture such as 6 % methane in air.After trying this burn-out procedure, remove the spark plug, insert a lightbulb through the

42、 spark plug hole, and inspect the vessel for cleanliness.Repeat the lean mixture explosion if necessary to clean the vessel.Mechanical means may also be used to remove unwanted carbon.10.16 Record the values for the highest fuel concentration,U1, that will propagate a flame and the lowest concentrat

43、ion,U2, above U1, that will not propagate a flame. Make duplicatetests on U2.E 918 83 (2005)3METHOD BFUEL WHICH MUST BE HEATED TOREACH ITS LIMITS OF FLAMMABILITY11. Procedure11.1 Set up the equipment as described in Method A exceptfor the introduction of fuel.Asmall cylinder of liquid fuel maybe pla

44、ced in the heated chamber with the test vessel or heatedseparately.NOTE 7The cylinder of liquid fuel must be fitted with a pressure-relief device which discharges outside the heated chamber and outside anyother structure which would confine the material. Fuels which mightundergo hazardous reaction i

45、n the heated cylinder must not be tested bythis procedure. If any uncertainty exists as to whether the sample mayreact in the heated chamber, thermal stability testing should be performed.11.2 Fit the fuel cylinder with a remotely controlled needlevalve. If the fuel will evaporate without fractionat

46、ion, place thevalve in contact with the vapor phase in the cylinder. Other-wise, place the needle valve in contact with the liquid phaseeven though this makes control of the flow more difficult.Connect the needle valve to the section of fill line holding thelow range pressure transducer. This allows

47、 the ball valveshown at the right side of this pressure transducer to be used tokeep fuel from condensing outside the heated chamber.11.3 After the vessel is evacuated, add the fuel componentfirst. With the desired amount of fuel pressure in the test vessel,proceed with the test starting with the la

48、st sentence of 10.2.12. Calculations12.1 Calculate the lower limit of flammability (LFL) andupper limit of flammability (UFL) from the values recorded in10.13 and 10.16.LFL 5 L11 L2! (1)UFL 5 U11 U2! (2)NOTE 8Limit concentrations are usually reported in terms of volumepercent. It is sometimes approp

49、riate to report limits in terms of weight perunit volume at the test conditions, particularly with multicomponent fuelsor materials exhibiting a high degree of nonideal vapor phase behavior.Report, for example, x mg/l at y MPa and zC.ANNEX(Mandatory Information)A1. DIMENSIONS AND SPECIFICATIONS OF APPARATUS (FIG. 1)A1.1 Test Vessel3A1.1.1 The test vessel shall be a metal vessel having avolume no less than 1 L and a minimum inside diameter of 7.6mm (3 in.). After fabrication, the vessel shall be satisfactorilytested to 20.68 MPa (3000 psi). Fig. 1 shows appar