简介:Inordertoinvestigatethefiresuppressioneffectivenessofwatermistwithmetalchlorideadditives,ultrafinewatermistsofthesesaltswithdiametersabout10μmwereintroducedintoCH4/airnon-premixedflameinthecupburner.Resultsshowedthatthesedropletshardtomakeitselftotheflamefrontunderthecupburnerflowconditionsfunctionedasacarrierofthevaporizedsolidparticlesoritsdecomposedmaterials.Themetalchlorideimprovedfiresuppressionefficacyofwatermistwhichwereaffectedbythetypeandconcentrationofmetalchloride.Onamassbasis,thereisafiresuppressioneffectivenessrelationshipofMgCl2
简介:采用静态箱—气相色谱法,以常规稻为参照对象,研究福州平原地区目前正在广泛推广的超级稻稻田的甲烷(CH4)和氧化亚氮(N2O)排放通量特征。结果表明,稻田CH4排放主要集中在水稻分蘖期,其CH4排放量分别占常规稻和超级稻稻田总排放量的76.7%和64.1%;常规稻稻田CH4排放通量范围为0.09~16.90mg/(m2·h),超级稻稻田CH4排放通量范围为0.11~14.30mg/(m·2h);在整个水稻种植期,超级稻稻田平均CH4排放通量比常规稻稻田约减少3.6%;常规稻稻田的平均N2O通量为7.7μg/(m·2h),超级稻稻田的平均N2O通量为18.0μg/(m·2h);水稻成熟期常规稻和超级稻稻田的N2O通量占总通量的50%以上,分别达到了55.7%和66.9%。从综合温室效应看,常规稻稻田的综合增温潜势为2264.5kg/hm2CO2,超级稻稻田的综合增温潜势为1977.04kg/hm2CO2,超级稻稻田的综合增温潜势比常规稻稻田低12.7%。在相同管理条件下,种植超级稻可以降低稻田的综合温室效应,并提高水稻产量。
简介:CH4emissionrateshavebeenmeasuredcontinuouslyfortheearlyriceof1988andlatericesof1987and1988duringentiregrowingseasonsinaricepaddyfieldinHangzhou,ZhejiangProvince,China,byusinganautomaticsamplingandanalyzingsystem.DuringmostpartsoftheseasonsCH4emissionratesshowedstrongdiurnalvariations.Bi-modepatternswiththehighestvalueintheafternoonandasecondpeakatmid-nightweregenerallyfoundfortheearlyrice,whilethehighestvalueswerealmostalwaysfoundinthenightforthelaterice.Bi-modepatternswithasecondpeakintheafternoonwerealsofoundduringthereproductivephaseofthelatericeplants.Thesediurnalvariationsmaybeexplainedbythediurnalvariationsofthesoiltemperatureandtheactivityofriceplants.Strongseasonalvariationswithonepeakinthetilleringstageandtwoduringthereproductivephaseofriceplantswereobservedforallthethreegrowingseasons.Theseasonalvariationsmaybeexplainedbytheactivityofriceplants,availabilityoforganicsubstratesinthesoil,andtheactivityofsoilbacteriarelatedtosoiltemperatures,FertilizationdidnotshowsignificanteffectsonthetotalseasonalCH4emissionsbutslightlychangedthepatternoftheseasonalvariationsoftheCH4emissionrates.Averagedoverthemeasuringperiodsand8spots,CH4emissionratesof7.8mgm-2h-1fortheearlyriceand28.6mgm-2h-1forthelatericewereobtained.Basedonthesemeasureddata,thetotalglobalemissionofCH4fromricepaddiesisestimatedtobeabout90Tg/yrrangingfrom70to110,accountingfor20%ofthetotalsourceofCH4.
简介:InthispaperweusedMOF-5andCu3(BTC)2toseparateCO2/CH4andCH4/N2mixturesunderdynamicconditions.Bothmaterialsweresynthesizedandpelletized,thusallowingforameaningfulcharacterizationinviewofprocessscale-up.ThematerialswerecharacterizedbyX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM).Byperformingbreakthroughexperiments,wefoundthatCu3(BTC)2separatedCO2/CH4slightlybetterthanMOF-5.BecausethecrystalstructureofCu3(BTC)2includesunsaturatedaccessiblemetalsitesformedviadehydration,itpredominantlyinteractedwithCO2moleculesandmoreeasilycapturedthem.Conversely,MOF-5withasuitableporesizeseparatedCH4/N2moreefficientlyinourbreakthroughtest.
简介:本文探讨(CH3Li)4中键的作用,通过计算,发现(CH3Li)4分子的面甲基结构比顶甲基结构要稳定;指出Li—Li间的成键作用相当强,约为Li2分子中键作用的40%左右,估计(CH3Li)4中的J7Li-6Li值约为1Hz。
简介:Alowpoweratmosphericpressureplasmajetdrivenbya24kHzACpowersourceandoperatedwithaCH4/airgasmixturehasbeeninvestigatedbyopticalemissionspectrometer.Theplasmaparametersincludingtheelectronexcitationtemperature,vibrationaltemperatureandrotationaltemperatureoftheplasmajetatdifferentdischargepowersarediagnosedbasedontheassumptionthatthekineticenergyofthespeciesobeystheBoltzmanndistribution.TheelectrondensityatdifferentpowerisalsoinvestigatedbyHβStarkbroadening.Theresultsshowthattheplasmasourceworksundernon-equilibriumconditions.Itisalsofoundthatthevibrationaltemperatureandrotationaltemperatureincreasewithdischargepower,whereastheelectronexcitationtemperatureseemstohaveadownwardtrend.Theelectrondensityincreasesfrom0.8×1021m-3to1.1×1021m-3whenthedischargepowerincreasesfrom53Wto94W.
简介:ThispaperpresentsabriefoverviewofCO2reformingofCH4(CRM)byvariousformsof'arc'plasma,whichismoresuitabletoCRM,andtheenergyefficiencyisusedtoevaluatedifferentplasmaprocessesspecifically.Accordingtothereportedresults,thearcthermalplasmawithbinodeexhibitedbetterperformance.Moreover,theplasmaCRMprocesswascomparedwiththereportedplasmasteamreformingofCH4(SRM)process,andtheresultsshowedthattheformerprocesshasadvantagesonenergyefficiencyandCH4consumption.Additionally,itisbelievedthattheplasmaCRMprocesswouldbecompetitivewiththeconventionalSRMprocessinbothenergyefficiencyandCO2emissiononcetheheatmanagementisemphasizedandtherenewablepowerisused.Finally,aconceptofplasmareactorforindustrialapplicationisproposed.
简介:MoleculardynamicssimulationsareperformedtostudythegrowthmechanismofCH4-CO2mixedhydrateinxCO2=75%,xCO2=50%,andxCO2=25%systemsatT=250K,255Kand260K,respectively.OursimulationresultsshowthatthegrowthrateofCH4-CO2mixedhydrateincreasesastheCO2concentrationintheinitialsolutionphaseincreasesandthetemperaturedecreases.Viahydrateformation,thecompositionofCO2inhydratephaseishigherthanthatininitialsolutionphaseandtheencagingcapacityofCO2inhydratesincreaseswiththedecreaseintemperature.ByanalysisofthecageoccupancyratioofCH4moleculesandCO2moleculesinlargecagestosmallcages,wefindthatCO2moleculesarepreferablyencagedintothelargecagesofthehydratecrystalascomparedwithCH4molecules.Interestingly,CH4moleculesandCO2moleculesfrequentlyreplacewitheachotherinsomeparticularcagesitesadjacenttohydrate/solutioninterfaceduringthecrystalgrowthprocess.Thesetwospeciesofguestmoleculeseventuallyacttostabilizethenewlyformedhydrates,withCO2moleculesoccupyinglargecagesandCH4moleculesoccupyingsmallcagesinhydrate.
简介:MicrodosimetricSpectrumandRadialDoseDistributionof239PnorRayinCH4Gas¥ZhuLianfang;LiXuekan;ChenXuebing;HeYusheng;SuYouwuand...
简介:Netemissioncoefficientsofradiationwerecalculatedforisothermalplasmaofmethaneasafunctionoftheplasmatemperature5,000~30,000Kandthearcradius0mmto10mmatatmosphericpressure.Calculationstakeintoaccountcontinuumandlineradiations,specialattentionhasalsobeengiventotheinfluenceofoverlappingspectrallines.ThelineshapesinourcalculationsaregivenbyconvolutionofDopplerandLorentzprofiles,resultinginasimplifiedVoigtprofile.Inthecaseofahydrogenprofile,weusedtheVidaltables,andthefourfirstLymanlinesandthefourfirstBalmerlineswereconsidered.Thiscalculationwascarriedoutontheassumptionoflocalthermodynamicequilibriumandinanondiffusiveenvironment.ThenetemissioncoefficientcalculationforpureargonplasmawascomparedwiththeexperimentalresultsofEvansinourpreviouswork.Weusedtheescapefactor,andourresultswerehigherthanthoseoftheexperiment.Inthispaper,weexplainwhy,usingtheescapefactor,theradiationisoverestimated.ThenetemissioncoefficientobtainedfromarealspectrumwascomparedwithEssoltaniwork’swhichusedtheline-by-linemethodforpureargonplasma.
简介:Attheambienttemperatureandpressureaglowdischargeplasmawasusedasanewapproachforthecouplingofmethanewiththenewly-developedrotarymultidentatehelixelectrode.Inthepresenceofhydrogen,theeffectsoftheinputpeakvoltagesandgasflowratesonmethaneconversion,C_2singlepassyieldandselectivitywereinvestigated,andthentheresultswerecomparedwiththosefromthethree-discmultidentateelectrode.Thisdemonstrated,onanexperimentalscale,thattherotarymultidentatehelixelectrodewasbetterthanthemultidentatethree-discelectrodeastherewaslittleaccumulationofcoke,andtheC_2yieldperpasswas69.85%andC_2selectivityover99.14%with70.46%methaneconversionataninputpeakvoltageof2300Vand60ml/mingasflowrate.
简介:CO2photoreductionisanattractiveprocesswhichallowsthestorageofsolarenergyandsynthesisofsolarfuels.Manydifferentphotocatalyticsystemshavebeendeveloped,whilethealternativephoto-reactorsarestillinsufficientlyinvestigated.Inthiswork,photoreductionofCO2withH2OintoCH4wasinvestigatedinamodifiedconcentratingsolarreactor,usingTiO2andPt/TiO2asthecatalysts.TheTiO2andPt/TiO2sampleswereextensivelycharacterizedbydifferenttechniquesincludingpowderX-raydiffraction(XRD),N2adsorption/desorptionandUV–visabsorption.ThecatalyticperformanceoftheTiO2andPt/TiO2samplesinthegasphasewasevaluatedunderunconcentratedandconcentratedXe-lamplightandnaturesolarlightwithdifferentconcentratingratios.VariousparametersofthereactionsystemandthecatalystswereinvestigatedandoptimizedtomaximizethecatalyticperformanceofCO2reductionsystem.Comparedwiththenormallightirradiation,theTiO2andPt/TiO2samplesshowhigherphotocatalyticactivity(about6–7times)forreducingCO2intoCH4underconcentratedXe-lamplightandnaturesolarlight.Intherangeofexperimentallightintensity,itisfoundthattheconcentrationofthelightmakesitsuitableforthecatalyticreaction,andincreasestheutilizationefficiencyoftheTiO2andPt/TiO2sampleswhiledoesnotdecreasethequantumefficiency.
简介:ThecrystalstructureofDi-nitratobis(ethylcaprolactam)uranyl(Ⅱ)UO2[CH2(CH2)4CONC2H5]2(NO3)2wasestablishedbyasingle-crystalX-raydiffractionstudy.Itistriclinie,spacegroupP1,witha=7.171(2),b=8.655(3),c=10.182(5)A,α=78.27(3),β=70.63(3),γ=81.76(3)°,V=581.7(4)A3,Z=l,Dc=1.94g.cm-3.FinalRvalueis0.0218.Theresultrevealsthaturanylioniscoordinatedtosixoxygenatoms,twoofthemarefromtwocarbonylgroupsofethylcaprolactamandtheotherfourarefromtwonitrategroups.