ImageVerifierCode 换一换
格式:PDF , 页数:4 ,大小:92.64KB ,
资源ID:528699      下载积分:5000 积分
快捷下载
登录下载
邮箱/手机:
温馨提示:
快捷下载时,用户名和密码都是您填写的邮箱或者手机号,方便查询和重复下载(系统自动生成)。 如填写123,账号就是123,密码也是123。
特别说明:
请自助下载,系统不会自动发送文件的哦; 如果您已付费,想二次下载,请登录后访问:我的下载记录
支付方式: 支付宝扫码支付 微信扫码支付   
验证码:   换一换

加入VIP,免费下载
 

温馨提示:由于个人手机设置不同,如果发现不能下载,请复制以下地址【http://www.mydoc123.com/d-528699.html】到电脑端继续下载(重复下载不扣费)。

已注册用户请登录:
账号:
密码:
验证码:   换一换
  忘记密码?
三方登录: 微信登录  

下载须知

1: 本站所有资源如无特殊说明,都需要本地电脑安装OFFICE2007和PDF阅读器。
2: 试题试卷类文档,如果标题没有明确说明有答案则都视为没有答案,请知晓。
3: 文件的所有权益归上传用户所有。
4. 未经权益所有人同意不得将文件中的内容挪作商业或盈利用途。
5. 本站仅提供交流平台,并不能对任何下载内容负责。
6. 下载文件中如有侵权或不适当内容,请与我们联系,我们立即纠正。
7. 本站不保证下载资源的准确性、安全性和完整性, 同时也不承担用户因使用这些下载资源对自己和他人造成任何形式的伤害或损失。

版权提示 | 免责声明

本文(ASTM E1445-2008 Standard Terminology Relating to Hazard Potential of Chemicals《化学品潜在危险性相关标准术语》.pdf)为本站会员(progressking105)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM E1445-2008 Standard Terminology Relating to Hazard Potential of Chemicals《化学品潜在危险性相关标准术语》.pdf

1、Designation: E 1445 08Standard Terminology Relating toHazard Potential of Chemicals1This standard is issued under the fixed designation E 1445; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number in

2、parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This standard is a compilation of terminology used inthe area of hazard potential of chemicals. Terms that aregenerally understood or adequately

3、defined in other readilyavailable sources are not included.1.2 Although some of these definitions are general in nature,many must be used in the context of the standards in whichthey appear. The pertinent standard number is given in paren-theses after the definition.1.3 In the interest of common und

4、erstanding and standard-ization, consistent word usage is encouraged to help eliminatethe major barrier to effective technical communication.2. Referenced Documents2.1 ASTM Standards:2E 476 Test Method for Thermal Instability of ConfinedCondensed Phase Systems (Confinement Test)E 487 Test Method for

5、 Constant-Temperature Stability OfChemical MaterialsE 537 Test Method for The Thermal Stability Of ChemicalsBy Differential Scanning CalorimetryE 582 Test Method for Minimum Ignition Energy andQuenching Distance in Gaseous MixturesE 659 Test Method for Autoignition Temperature of LiquidChemicalsE 68

6、0 Test Method for Drop Weight Impact Sensitivity OfSolid-Phase Hazardous MaterialsE 681 Test Method for Concentration Limits of Flammabil-ity of Chemicals (Vapors and Gases)E 698 Test Method for Arrhenius Kinetic Constants forThermally Unstable Materials Using Differential ScanningCalorimetry and th

7、e Flynn/Wall/Ozawa MethodE 771 Test Method for Spontaneous Heating Tendency ofMaterials3E 918 Practice for Determining Limits of Flammability ofChemicals at Elevated Temperature and PressureE 1226 Test Method for Pressure and Rate of Pressure Risefor Combustible DustsE 1231 Practice for Calculation

8、of Hazard PotentialFigures-of-Merit for Thermally Unstable MaterialsE 1232 Test Method for Temperature Limit of Flammabilityof ChemicalsE 1491 Test Method for Minimum Autoignition Tempera-ture of Dust CloudsE 1515 Test Method for Minimum Explosible Concentra-tion of Combustible DustsE 1981 Guide for

9、 Assessing Thermal Stability of Materialsby Methods of Accelerating Rate CalorimetryE 2012 Guide for the Preparation of a Binary ChemicalCompatibility ChartE 2019 Test Method for Minimum Ignition Energy of aDust Cloud in AirE 2021 Test Method for Hot-Surface Ignition Temperatureof Dust LayersE 2046

10、Test Method for Reaction Induction Time by Ther-mal Analysis3. Terminology3.1 Definitions:adiabatic calorimeter, nan instrument capable of makingcalorimetric measurements while maintaining a minimalheat loss or gain between the sample and its environment,which is verifiable by the capability to cont

11、inuously measurethe temperature differential between the sample and itssurroundings. (E 1981)adiabatic decomposition temperature rise, (T)d, nan esti-mation of the computed temperature which a specimenwould attain if all of the enthalpy (heat) of decompositionreaction were to be absorbed by the samp

12、le itself. Highvalues represent high hazard potential. (E 1231)anvil, nthe smooth, hardened surface upon which the testsample or cup containing the sample rests. (E 680)Arrhenius equationk = ZeE/RTwhere k is the specificreaction rate constant in reciprocal minutes for first order, Zis the pre-expone

13、ntial factor in reciprocal minutes, E is theArrhenius activation energy in J/mol, R is the gas constant,8.32 J/mol K, and T is the temperature in kelvin. (E 698)1This terminology is under the jurisdiction ofASTM Committee E27 on HazardPotential of Chemicals and is the direct responsibility of Subcom

14、mittee E27.01 onEditorial and Nomenclature.Current edition approved May 15, 2008. Published July 2008. Originallyapproved in 1991. Last previous edition approved in 2003 as E 1445 03.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.

15、org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Withdrawn.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.autoignition, nthe ignition of a material commonly i

16、n air asthe result of heat liberation due to an exothermic oxidationreaction in the absence of an external ignition source such asa spark or flame. (E 659)autoignition temperature, nthe minimum temperature atwhich autoignition occurs under the specified conditions oftest. (E 659)DISCUSSIONAutoigniti

17、on temperature is also referred to as sponta-neous ignition temperature, self-ignition temperature, autogenous igni-tion temperature, and by the acronyms AIT and SIT. AIT is the lowesttemperature at which the substance will produce hot-flame ignition inair at atmospheric pressure without the aid of

18、an external energy sourcesuch as spark or flame. It is the lowest temperature to which acombustible mixture must be raised, so that the rate of heat evolved bythe exothermic oxidation reaction will over-balance the rate at whichheat is lost to the surroundings and cause patibility, adjthe ability of

19、 materials to exist in contactwithout specified (usually hazardous) consequences under adefined scenario. (E 2012)constant-temperature stability (CTS) value, nthe maxi-mum temperature at which a chemical compound or mixturemay be held for a 2-h period under the conditions of the testwithout exhibiti

20、ng a measurable exothermic reaction.(E 487)cool-flame, na faint, pale blue luminescence or flameoccurring below the autoignition temperature (AIT).(E 659)DISCUSSIONCool-flames occur in rich vapor-air mixtures of mosthydrocarbons and oxygenated hydrocarbons. They are the first part ofthe multistage i

21、gnition process.critical half thickness, (a), nan estimation of the halfthickness of a sample in an unstirred container, in which theheat losses to the environment are less than the retained heat.This buildup of internal temperature leads to a thermal-runaway reaction. (E 1231)critical temperature,

22、(Tc), nan estimation of the lowesttemperature of an unstirred container at which the heatlosses to the environment are less than the retained heatleading to a buildup of internal temperature. This tempera-ture buildup leads to a thermal-runaway reaction. (E 1231)DISCUSSIONThis description assumes pe

23、rfect heat removal at thereaction boundary. This condition is not met if the reaction takes placein an insulated container such as when several containers are stackedtogether or when a container is boxed for shipment. These figures-of-merit underestimate the hazard as a result of this underestimatio

24、n ofthermal conductivity.deflagration index, (KSt), nmaximum dP/dt normalized to a1.0 m3volume. It is measured at the optimum dust concen-tration. KStis defined according to the following cubicrelationship:KSt5 dP/dt!maxV1/3where:P = pressure, (bar)t = time, (s)V = volume, (m3)KSt= (bar m/s)(E 1226)

25、differential scanning calorimetry (DSC), na technique inwhich the difference in energy inputs into a substance and areference material is measured as a function of temperature,while the substance and the reference material are subjectedto a controlled temperature program. (E 698)DISCUSSIONTwo modes,

26、 power compensation differential scanningcalorimetry (power compensation DSC) and heatflux differential scan-ning calorimetry (heatflux DSC), can be distinguished depending on themethod of measurement used.differential thermal analysis (DTA), na technique in whichthe temperature difference between a

27、 substance and refer-ence material is measured as a function of temperature whilethe substance and the reference material are subjected to acontrolled temperature program. (E 698)(dP/dt)ex, nthe maximum rate of pressure rise during thecourse of a single deflagration. (E 1226)(dP/dt)max, nmaximum val

28、ue for the rate of pressure in-crease per unit time reached during the course of a defla-gration for the optimum concentration of the dust tested. It isdetermined by a series of tests over a large range ofconcentrations. It is reported in bar/s. (E 1226)drop weight, nthat weight which is raised to a

29、 selectedheight and released. This weight does not impact the sampledirectly; rather it strikes another stationary weight that is incontact with the sample. (E 680)DTA(DSC) curve, na record of a thermal analysis where thetemperature difference (DT) or the energy change (Dq)isplotted on the ordinate

30、and temperature or time is plotted onthe abscissa (see Figs. 3 and 4). (E 537)dust concentration, nthe mass of dust divided by theinternal volume of the test chamber. (E 1491)extrapolated onset temperature, nempirically, the tem-perature found by extrapolating the baseline (prior to thepeak) and the

31、 leading side of the peak to their intersection(see Fig. 3). (E 537)final temperature (Tfinal),nthe lowest temperature, cor-rected to a pressure of 101.3 kPa (760 mm Hg, 1013 mbar),at which application of an ignition source causes the vaporsof the specimen to ignite under specified conditions of tes

32、t.(E 1232)flash point , nthe observed system temperature at the end ofan exotherm, generally at the temperature where the self-heat rate of the reaction has decreased below the operator-defined slope sensitivity threshold. (1981) (E 1232)general rate lawdC/dt = k (1 C)nwhere C is fractionalconversio

33、n, t is the time in minutes, and n is the reactionorder. (E 698)guide bushing, nthe steel bushing that surrounds, aligns,and holds the stationary intermediate weight in place.(E 680)guide system, nthe rails, wires, and shaft that guide the dropweight during its fall. (E 680)hot-surface ignition temp

34、erature of a dust layer, nlowestset temperature of the hot plate that causes ignition of thedust layer. (E 2021)H50value, na drop height with a 50 % probability ofreaction, as determined experimentally by the Brucetonup-and-down method. (E 680)E 1445 082ideal adiabatic temperature rise (DTad), nthe

35、temperaturerise which would be observed in an exothermic reaction if allof the heat liberated were used to increase the temperature ofonly the sample. It is conveniently calculated as the productof the observed adiabatic temperature rise, DTobs, and thethermal inertia factor, f. (E 1981)ignition, nt

36、he initiation of combustion. (E 659)ignition delay time, nthe time lapse between application ofheat to a material and its ignition. It is the time in secondsbetween insertion of the sample into the flask and ignition. Itis maximum at the minimum autoignition temperature andalso referred to as igniti

37、on lag. (E 659)ignition delay time, td, nexperimental parameter defined asthe time interval between the initiation of the dust dispersionprocedure (the time at which the dispersion air starts to enterthe chamber) in an experimental apparatus and the activationof the ignition source. The ignition del

38、ay time characterizesthe turbulence level prevailing at ignition under the definedtest conditions. (E 1226)ignition of a dust layer, ninitiation of self-heating orcombustion in a material under test. (E 2021)ignition quenching distance, nMaximum spacing betweenelectrode flanges that will not permit

39、spark ignition andflame propagation beyond the flanges, when tested under thespecified test conditions. (E 582)ignition time, ntime between the start of heating and thepoint at which the maximum temperature or flaming com-bustion is reached. (E 2021)impact apparatus or machine, nthe total apparatus

40、includ-ing the foundation parts, guide rails, electromagnet lift,winch, and tools. (E 680)impact tool, nthe drop weight, intermediate weight, andanvil. (E 680)lower limit of flammability or lower flammable limit (LFL),nthe minimum concentration of a combustible substancethat is capable of propagatin

41、g a flame through a homoge-neous mixture of the combustible and a gaseous oxidizerunder the specified conditions of test. (E 681)lower temperature limit of flammability, (LTL), nthelowest temperature, corrected to a pressure of 101.3 kPa(760 mm Hg, 1013 mbar), at which application of an ignitionsour

42、ce causes a homogeneous mixture of a gaseous oxidizerand vapors in equilibrium with a liquid (or solid) specimento ignite and propagate a flame away from the ignitionsource under the specified conditions of test. (E 1232)minimum autoignition temperature (MAIT), nthe mini-mum temperature at which a d

43、ust cloud will self ignite underthe specified conditions of test. (E 1515)minimum explosible concentration (MEC), nthe mini-mum concentration of a combustible dust cloud that iscapable of propagating a deflagration through a well dis-persed mixture of the dust and air under the specifiedconditions o

44、f test (E 1491)minimum ignition energy, nelectrical energy dischargedfrom a capacitor, which is just sufficient to effect ignition ofthe most ignitable mixture of a given fuel-mixture underspecific test conditions. (E 2019)observed adiabatic temperature rise (DTobs), nthe ob-served temperature rise

45、in the system during an exotherm;mathematically, it is equal to the temperature differencebetween the final temperature and the onset temperature ofan exotherm. (E 1981)onset temperature, nthe temperature at which a deflectionfrom the established baseline is first observed. (E 537)onset temperature

46、(Tstart), nthe observed system tempera-ture at the start of an exotherm where the self-heating ratefirst exceeds the operator-defined slope sensitivity threshold,usually 0.02C/min; the onset temperature is not a funda-mental property of a substance, but is apparatus-dependent,based upon the inherent

47、 sensitivity of the calorimetricsystem (1981)Pex, nthe maximum explosion pressure (above the pressurein the vessel at the time of ignition) reached during thecourse of a single deflagration test. (E 1226)Pignition, nthe absolute pressure at the time of ignition.(E 1515)Pex,a, nthe maximum explosion

48、pressure (absolute) reachedduring the course of a single deflagration test. (E 1515)DPignitor, nthe pressure rise in the chamber due to the ignitorby itself. (E 1515)Pmax, nthe maximum pressure (above pressure in the vesselat the time of ignition) reached during the course of adeflagration for the o

49、ptimum concentration of the dusttested. Pmaxis determined by a series of tests over a largerange of concentrations. It is reported in bar. (E 1226)peak, nthat part of a DTAor DSC curve which is attributableto the occurrence of a single process. It is normally charac-terized by a deviation from the established base line, amaximum deflection, and a reestablishment of a base line notnecessarily identical to that before the peak. (E 698)peak, nthat portion of a heating curve which is attributableto the occurrence of

copyright@ 2008-2019 麦多课文库(www.mydoc123.com)网站版权所有
备案/许可证编号:苏ICP备17064731号-1