ASTM D4084-2007(2017) Standard Test Method for Analysis of Hydrogen Sulfide in Gaseous Fuels (Lead Acetate Reaction Rate Method)《分析气体燃料中硫化氢的标准试验方法(醋酸铅反应速率法)》.pdf

《ASTM D4084-2007(2017) Standard Test Method for Analysis of Hydrogen Sulfide in Gaseous Fuels (Lead Acetate Reaction Rate Method)《分析气体燃料中硫化氢的标准试验方法(醋酸铅反应速率法)》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4084-2007(2017) Standard Test Method for Analysis of Hydrogen Sulfide in Gaseous Fuels (Lead Acetate Reaction Rate Method)《分析气体燃料中硫化氢的标准试验方法(醋酸铅反应速率法)》.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4084 07 (Reapproved 2017)Standard Test Method forAnalysis of Hydrogen Sulfide in Gaseous Fuels (LeadAcetate Reaction Rate Method)1This standard is issued under the fixed designation D4084; 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 () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers the determination of hydrogensulfide (H2S) in gaseous fuels. I

3、t is applicable to the measure-ment of H2S in natural gas, liquefied petroleum gas (LPG),substitute natural gas, landfill gas, sewage treatment off gasses,recycle gas, flare gasses, and mixtures of fuel gases. Thismethod can also be used to measure the hydrogen sulfideconcentration in carbon dioxide

4、. Air does not interfere. Theapplicable range is 0.1 to 16 parts per million by volume(ppm/v) (approximately 0.1 to 22 mg/m3) and may be extendedto 100 % H2S by manual or automatic volumetric dilution.1.2 This standard does not purport to address all of thesafety concerns, if any, associated with it

5、s use. It is theresponsibility of the user of this standard to establish appro-priate safety, health, and environmental practices and deter-mine the applicability of regulatory limitations prior to use.1.3 This international standard was developed in accor-dance with internationally recognized princ

6、iples on standard-ization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recom-mendations issued by the World Trade Organization TechnicalBarriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent

7、WaterD1914 Practice for Conversion Units and Factors Relating toSampling and Analysis of AtmospheresD2420 Test Method for Hydrogen Sulfide in LiquefiedPetroleum (LP) Gases (Lead Acetate Method)D3609 Practice for Calibration Techniques Using Perme-ation TubesD7166 Practice for Total Sulfur Analyzer B

8、ased On-line/At-line for Sulfur Content of Gaseous FuelsE2165 Practice for Establishing an Uncertainty Budget forthe Chemical Analysis of Metals, Ores, and RelatedMaterials (Withdrawn 2007)33. Summary of Test Method3.1 Measurement of H2S is accomplished by ratiometricallycomparing a reading of an un

9、known sample with that of aknown standard using a differential colorimetric detection.Pure H2S is used as a primary standard and mixed volumetri-cally with a sulfur free matrix gas that is ideally similar incomposition to the sample gas. A gaseous sample at constantflow is humidified and passed over

10、 lead-acetate-impregnatedpaper. H2S reacts with lead acetate to form a brown stain on thepaper. The rate of reaction and resulting rate of color change isproportional to the concentration of H2S in the sample. Theanalyzer is comprised of an optical system, a photon detectionsystem, a signal differen

11、tiation system of first order, and asignal output system. When there is no change in the color ofthe tape, and no resulting change in photodetector output, E,the first derivative, dE/dt, is zero. This results in an analyzerthat automatically zeroes when there is no H2S.4. Significance and Use4.1 Thi

12、s test method is useful in determining the concentra-tion of hydrogen sulfide in gaseous samples and in verifyingcompliance with operational needs and/or environmental limi-tations for H2S content. The automated performance operationof this method allows unattended measurement of H2S con-centration.

13、 The user is referred to Practice D7166 for unat-tended on-line use of instrumentation based upon the leadacetate reaction rate method.5. Apparatus5.1 Volumetric Measuring DevicesA graduated 10-L cyl-inder (see Fig. 1) having a movable piston for volumetricallymeasuring test gas. Gastight syringes o

14、f 0.1 and 0.5-mLvolume for volumetrically measuring 100 % H2S. Gas tight1This test method is under the jurisdiction ofASTM Committee D03 on GaseousFuels and is the direct responsibility of Subcommittee D03.05 on Determination ofSpecial Constituents of Gaseous Fuels.Current edition approved Nov. 1, 2

15、017. Published December 2017. Originallyapproved in 1981. Last previous edition approved in 2012 as D4084 07(2012).DOI: 10.1520/D4084-07R17.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volum

16、e information, refer to the standards Document Summary page onthe ASTM website.3The last approved version of this historical standard is referenced onwww.astm.org.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United StatesThis international stand

17、ard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.1syring

18、es of other volumes can be used. These graduateddevices are not needed when the permeation tube method ofdynamic mixing is used to prepare the reference sample sincethis method will generate a reference mixture.5.2 Sample PumpA pump capable of providing more than8 mL/s (approximately 1 ft3/h) or les

19、s than 1 mL/s at 70 kPa(approximately 10.15 psig). Gas-wetted parts are ideally con-structed from either aluminum or polytetrafluorethylene(PTFE). Stainless steel may be used when higher safety thanafforded by aluminum or PTFE is required.5.3 Colorimetric Rate of Reaction SensorSelect a deviceof suf

20、ficient sensitivity to measure a minimum rate of changeof color density corresponding to 0.1-ppm H2S by volume inthe sample gas. (See Fig. 2.)5.4 Recorder, having an adjustable span of 1 to 10-V fullscale with an input impedance of 1 M or higher. A printer orother output means, such as a data logger

21、 or DistributedControl System (DCS) , can be used.6. Reagents and MaterialsNOTE 1Warning: Hydrogen Sulfide contained in lecture bottles,permeation tubes or compressed gas cylinders may be flammable andharmful or fatal if ingested or inhaled. Lecture bottles, permeation tubesand compressed gas standa

22、rds should only be handled in well ventilatedFIG. 1 Calibration Sample Preparation Cylinder withMovable PistonFIG. 2 Flow System for H2S Measurement Showing Calibration, LPG, and Gaseous Sample ConnectionsD4084 07 (2017)2locations away from sparks and flames. Improper handling of compressedgas cylin

23、ders containing air, nitrogen or hydrocarbons can result inexplosion. Rapid release of nitrogen or hydrocarbon gasses can result inasphyxiation. Compressed air supports combustion.6.1 Acetic Acid SolutionAdd 50 mL of glacial acid(CH3COOH) to distilled water or dionized water to make 1 Lof solution (

24、5 %). Type II distilled water as specified inSpecification D1193 is satisfactory for the dilution. Waterdionized to 1 megaohm-centimeter is also satisfactory for thedilution.6.2 Reference Gas:6.2.1 Hydrogen Sulfide Source99.5 % by volume purity orbetter. An alternative H2S source is an H2S mixture o

25、btainedusing permeation tube procedures. Hydrogen sulfide generatedfrom a solid heated to generate H2S may be used instead of aH2S source if desired. H2S contained in permeation tubes orcompressed gas cylinders may be flammable and harmful orfatal if ingested or inhaled. Permeation tubes and compres

26、sedgas standards should only be handled in well ventilatedlocations away from sparks and flames. (WarningHydrogensulfide is an extremely toxic gas.)6.2.2 Dilution GasesChemically pure grade or purifiedgas. Blend or obtain a sulfur-free gas of the same relativedensity as the sample gas to be analyzed

27、. Blends of gases, ofsimilar composition to the sample gas, are prepared from puregases by mixing, using a 10-L cylinder with piston. Pipelinegas scrubbed through activated charcoal and sodiumhydroxide-asbestos absorbent is satisfactory.6.2.3 Gas MixturesAnother alternative H2S source is acertified

28、H2S mixture obtained from a gas standard vendor.Such mixtures are in a sulfur free carrier gas that is of the sametype, or a close approximation, as the gas to be analyzed. Thesemixtures can be either a primary standard, which is then dilutedto the desired H2S concentration using a 10-L cylinder wit

29、h apiston, or a standard in a pressurized cylinder containing thedesired H2S concentration. Because of the potential fordegradation, H2S mixtures obtained from a gas standardvendor must be properly stored and used only within the statedcertification period. In the event of a discrepancy, H2S mixture

30、sprepared from a 99.5 % by volume or better purity H2S lecturebottle or obtained using permeation tube procedures must beused.6.2.3.1 Compressed Gas StandardsThe protocol for com-pressed gas standards contained in the appendix can be used toensure uniformity in compressed gas standard manufacture an

31、dprovide for traceability to a NIST or NMi reference material.6.2.3.2 Compressed gas standard regulators must be appro-priate for the delivery of sulfur gases and attached fittings mustbe passivated or inert to sulfur gases.6.3 Lead Acetate Sensing PaperPrepare in accordancewith Test Method D2420, u

32、sing appropriate size strips anddrying in an H2S-free environment. Commercially availabletest paper has been found satisfactory. Used Lead AcetateSensing Paper should be disposed of in accordance with local,state, and/or federal environmental regulations.6.4 Permeation DevicesHydrogen Sulfide standa

33、rds canbe prepared using a permeation tube gravimetrically calibratedand certified at a convenient operating temperature.At constanttemperature, calibration gases covering a wide range of con-centration can be generated by varying and accurately measur-ing the flow rate of diluent gas passing over t

34、he tubes. Thesecalibration gases are used to calibrate the analyzer.6.4.1 Permeation System Temperature ControlPermeationdevices are maintained at the calibration temperature within0.1C.6.4.2 Permeation System Flow ControlThe permeationflow system measures diluent gas flow over the permeationtubes w

35、ithin 62 percent.6.4.3 Permeation tubes are inspected and weighed to thenearest 0.01 mg on at least a monthly basis using a balancecalibrated against NIST traceable “S” class weights or theequivalent. Analyte concentration is calculated by weight lossand dilution gas flow rate as per Practice D3609.

36、 These devicesare discarded when the liquid contents are reduced to less thanten (10) percent of the initial volume or when the permeationsurface is unusually discolored or otherwise compromised.Used permeation tubes should be disposed of in accordancewith local, state, and/or federal environmental

37、regulations.7. Sampling7.1 Because of the chemical activity and adsorptive proper-ties of H2S, it is highly desirable to connect the test apparatusdirectly to the sample source using minimum lengths ofstainless steel, hastalloy, aluminum or fluorocarbon samplelines. Do not use copper containing, tha

38、t is, brass or copperflow system parts. In the event that direct sampling is notpractical, clean aluminum, stainless steel, or fluorocarbon linedsample containers may be used. Tedlar bags with inert fittingssuch as polypropylene or equivalent and silica lined samplecontainers can also be used for sa

39、mple collection. Tedlar bagscontaining sample require protection from light and heat. Thecollection of samples that are either in two phases or that willform two phases before analysis can be performed must beavoided. The presence of liquids causes H2S to partitionunequally between the liquid and ga

40、s phases. Such a partitionof H2S results in inaccurate measurement of H2S content.Samples must be analyzed with as little delay as possible andreported as “proximate analyses from cylinders” with length ofresidence time noted. Because of the broad reactivity of H2S,an extended delay between obtainin

41、g the sample and analyzingthe sample can result in inaccurate results.NOTE 2Each new sample container to be used for a test specimen canbe filled with a sample and analyzed over a period of time and theresulting data examined to determine the rate of deterioration of thesample. Repeated filling with

42、 a representative sample will tend topassivate a container. Approximately 10 L (approximately13 ft3)ofsample, at atmospheric pressure, is convenient for analysis and willnormally not deteriorate appreciably within 1 h. Slow instrument responseto changes in H2S concentration indicates the need for a

43、thorough cleaningof the flow system. (See Appendix X1 for a suggested cleaning proce-dure.) Errors caused by ambient temperature and pressure changes arecompensated for by comparison to a reference standard prepared at thetime of analysis. Preparation of the reference sample is described inSection 1

44、1.8. Instrument Preparation8.1 Fill a humidifier or humidifying bubbler to the full markwith acetic acid solution. The acetic acid minimizes someinterfering species. Set the range of the analyzer for the rangeD4084 07 (2017)3expected in the sample. Connect the pump and set theflowmeter for a nominal

45、 flow of 8 mL/s (approximately 1ft3/h). Note: analyte gas can also be delivered to the analyzerby use of a compressed gas cylinder or a permeation tubedevice.Alternative flow settings, such as a nominal 1 mL/s, canbe used. Obtain a blank reading by flowing dilution gasthrough the analyzer. Record th

46、e reading of the blank sample asB in 12.1. Do not adjust the instrument zero until verificationis obtained, that the room air or the carrier gas does not containH2S. Verification is accomplished by analyzing a room air orcarrier gas sample after it has been passed through an activatedcharcoal filter

47、 absorbent.9. Calibration9.1 Immediately after preparing the calibration standard,obtain its response on the analyzer. Practice D3609 is accept-able as an alternative method for preparation of a referencestandard. Certified compressed gas calibration standards ob-tained from a gas standard vendor ca

48、n also be used to calibratethe analyzer. The analyzer response is recorded as C in 12.1.Atleast twenty (20) discrete response replicates should be ob-tained to adequately demonstrate the statistical repeatability ofthe analyzer at two times the standard deviations about themean. If the analyzer repe

49、atability response fall outside of thepublished repeatability specifications then appropriate correc-tive action must be taken and the repeatability response of theanalyzer must be redetermined.10. Sample Measurement Procedure10.1 Sampling and Preparation of SamplesAppropriatesampling procedures are critical for meaningful hydrogensulfide determinations and must be tailored to the particularsample source.10.1.1 SamplesSamples are delivered to the laboratory inTedlar bags with polypropylene fittings or other inert fittings atatmospheric pressure, protected from