简介:Inordertofurtherreducethesulfurcontentingasoline,anewdesulfurizationprocesswasproposedbyusingcatalyticoxidationandextractionrealizedinanelectrochemicalfluidizedreactor.Thefluidizedlayerofloadedcatalystparticlesconsistedofleaddioxide(PbO2)supportedonactivatedcarbonparticles(PbO2/C)andtheelectrolytewasaqueousNaOHsolution.ThePbO2/Cparticleanodescouldremarkablyacceleratetheelectrochemicalreactionrateandpromotetheelectrochemicalcatalysisofsulfurcompounds.Thesulfurcompoundswereatfirstoxidizedtosulfonesorsulfoxides,whichwerethenremovedafterextraction.Theexperimentalresultsindicatedthattheoptimaldesulfurizationconditionswereasfollows:Thecellvoltagewas3.2V,theconcentrationofhydroxylionsinelectrolytewas0.12mol/L,andthefeedratewas300mL/min.Undertheseconditionstheconcentrationofsulfuringasolinewasreducedfrom310ppmto70ppm.Basedontheseexperimentalresults,amechanismofindirectelectrochemicallycatalyticoxidationwasproposed.
简介:Inordertomeettheurgentneedforreducingolefincontentincrackednaphtha,theinfluenceoffeedstockcharacteristicsontheolefincontentwasdiscussed.ThedifferenttypesandperformanceofcatalystsdevelopedbyRIPPwereintroduced.Moreover,someeffectiveoperationapproachesincommercialunitswerepresentedtoserveasareferencetotherefinersforcatalystselection.
简介:在FCC汽油的硫混合物的形成上的石蜡的效果在在从400~500的温度联合起来的一张小规模的固定的使流体化的床(FFB)上被学习,重量时时10h-1的空间速度(WHSV),和6的催化剂/油比率。结果证明在FCC汽油包含的C4-C6石蜡能与H2S反应主要形成thiophenes,alkyl-thiophenes以及thiols的部分数量,当象heptene那样的大分子的石蜡能与形成benzothiophenes的氢硫化物反应时。在不同催化剂上在不同温度形成的硫混合物的数量与在化工物品的石蜡的集体部分成比例,与在REUSY催化剂超过上形成的硫混合物的数量,那些在石蜡变换的度上由于催化剂性能的效果和催化剂的影响在形状上形成了选择沸石催化剂。因为为硫的形成的热力学、运动的常数上的温度的影响,在450点的最大值和在400点的最小象在石蜡变换degree.Based上一样加重在上的产生的硫混合物和他们到达的增加的数量上述学习,为与H2S在FCC汽油在石蜡的反应之上产生的硫混合物的预言的一个反应网络和一个模型被建立。
简介:Therestrictiononsulfurlevelingasolinehasbeenincreasinglytightened.TheU.S.TierⅡregulationrequiresareductionfromaverage340ppmto30ppmfrom2004to2008.Recentlysignificantprogresshasbeenmadeineffectivehighsulfurremoval,suchasposttreatmentofFCCgasolinebyselectivehydrotreating,SZorbsulfurremovaltechnology,OATSprocessetc.ThesulfurcontentofFCCgasolinecanbedeceasedtolessthan10ppm.WithregardtogasolinepoolcompositioninChina,itisveryimportanttolookforeffectivedesulfurizationprocessesthataresimple,straightforward,withlesshydrogenconsumption.Post-treatmentofFCCgasolineisapreferredoption.Fromthepointofviewofcomprehensiveutilization,alkylation,polymerization,isomerisationetc.canbeaddedtodesulfurizationprocesstomeettherequirementofultralowsulfur,premium.
简介:Recentlytheproject'Developmentofpackagetechnologyforregenerationofstyrenethroughextractivedistillationofpyrolysisgasoline(STED)'undertakenjointlybytheSINOPECResearchInstituteofPetroleumProcessing(RIPP)andotherinstitutionshaspassedtheappraisalheldinBeijing.Theexpertgroupattendingtheappraisal
简介:Thisarticleanalyzedtheproblemsarisingfromretrofittingthe800kt/avirgindieselhydrofiningunitintoa1.0Mt/aOCT-MgasolineHDSunitattherefineryofLuoyangPetrochemicalCompany,andtheoptimizedmeasuresaimedatimprovementsinoperationofHDSunit.ThepreliminarycalibrationresultshaveindicatedthehighdesulfurizationrateandgoodselectivityoftheHDStechnologytofulfillthedemandofLuoyangPetrochemicalCompanyforproductqualityupgradingwiththetargetsoftechnicalrevampfullyimplemented.
简介:In4-strokeinternalcombustionengines,air-fuelratiocontrolisachallengingtaskduetotherapidchangesofenginethrottle,especiallyduringtransientoperation.Toimprovethetransientperformance,managingthecycle-to-cycletransientbehaviorofthemassoftheair,thefuelandtheburntgasisakeyissueduetotheimbalanceofcycliccombustionprocess.Thispaperaddressthemodel-basedestimationandcontrolproblemforcyclicair-fuelratioofspark-ignitionengines.Adiscrete-timemodelofair-fuelratioisproposed,whichrepresentsthecycle-to-cycletransientbehaviorofin-cylinderstatevariablesundertheassumptionsofcyclicmeasurabilityofthetotalin-cylinderchargemass,combustionefficiencyandtheresidualgasfraction.Withthemodel,aKalmanfilter-basedair-fuelratioestimationalgorithmisproposedthatenableustoperformafeedbackcontrolofair-fuelratiowithoutusinglambdasensor.Finally,experimentalvalidationresultisdemonstratedtoshowtheeffectivenessofproposedestimationandcontrolschemethatisconductedonafull-scaledgasolineenginetestbench.
简介:减少硫的功能的部件--吊楔酸硷的对化合物--并且联系活跃沸石部件被开发为在汽油减少硫内容准备RFCC催化剂DOS。催化剂评估的结果表明了酸硷的对化合物在此开发了的吊楔能提高分子的硫由催化剂加重支持desulfurization反应继续的宏的变换,并且酸硷的对化合物能毫无疑问减少的选择沸石和吊楔的合作行动在汽油的石蜡和硫内容。因此开发的催化剂DOS的重油变换能力更高结合了一个提高的电阻到重金属污染在超过20%在汽油减少硫内容。在西诺佩克·久贾恩格·布朗奇公司的这催化剂的商业应用程序表明了与GRV-C催化剂相比,催化剂DOS获得的油泥浆收益在汽油与一种改进coke选择,增加的全部的液体收益,和一个减少的石蜡内容一起被减少。在汽油/硫在的硫的比率喂油能被20.3m%减少。
简介:Thehighshearagitationdevicewasfirstadoptedforgasolinedesulfurizationbyionicliquids.Theeffectofbenzylimidazolfluoborateindesulfurizationofgasolineandtheinfluenceofmoistureondeuslfurizationratewereinvestigated.Theexperimentalresultsshowedthattheionicliquidcouldeffectivelydecreasethesulfurcontentofgasolineandtheoptimalconditionswereasfollows:Thereactioncouldbecarriedoutatroomtemperature,avolumetricratiobetweenoilandtheliquidof2∶1,avolumetricratiobetweenwaterandionicliquidof0.04∶1,arotationalspeedof5krad/s,andareactiontimeof1minute.Thedesulfurizationrateofgasolinereached53.6%,andthegasolineyieldwasupto97.3%.Theionicliquidcouldberecycledforrepeateduse,andtheuseofhighshearagitationforgasolinewouldhavegoodprospects.
简介:<正>NaYzeolitewasmodifiedthroughdealuminationwithoxalicacid,andtheHYzeolitewasobtainedbycalcinationofthemodifiedNaYzeolite.Thezeolitemoldingprocesswascarriedoutatambienttemperature(25℃),andtheinfluenceofsolid/fuelmassratioandadsorptivedesulfurizationtimeontheHYzeolitewereinvestigatedthroughtestsonstaticselectiveadsorptivedesulfurizationofFCCgasolinecontainingorganicsulfurcompounds(withaScontent=135ppm).ThesulfurcontentandsulphidetypesintheFCCgasolinewereanalyzedbyaGC2010sulfuranalyzerandaGC-SCDchromatograph.ThetestresultsshowedthatthemoldedHYzeolitewasbetterthantheunmoldedHYzeolite.AtastaticadsorptivedesulfurizationtimeonthemoldedHYzeoliteequatingto6hours,asolid/fuelmassratioof1:3,thesulfurcontentofFCCgasolinewasdecreasedto30ppm,andthedesulfurizationratewasequalto78%.WhenthebreakthroughpointofthemoldedHYwasequalto50ppm,themoldedHYzeolitewascapableofadsorbing4.86mgofsulfurpergramofadsorbent.AndtheregenerationrateofmoldedHYzeolitewasequalto98%.
简介:AseriesofCoMo/Al2O3catalystsforselectivehydrodesulfurization(HDS)ofgasolinewerestudiedwithRamanspectroscopy,apowerfulmethodthatcreatesspecifcsignalsforthestatesandthedistributionsofoxidicprecursorsandsulfdedactivephases.ThehighertheMoandCo,thelowerthetetrahedrallycoordinatedmolybdate,andthehigherthepolymolybdate.ButtheamountofpolymolybdatedecreasedwhenCoMoO4appeared.Cobalt-promotedpolymolybdatewastheprecursor,anditsrelativecontentcorrelatedwellwiththeHDSselectivity.Forsulfdedcatalysts,addingthecobalt-promoterledtolocaldistortion-disorderoftheMoS2structureandtheformationofaCoMoSphase.Thismethodcanprovideimportantinformationfordesigningnewindustrialselective-HDScatalysts.
简介:Thispaperhasinvestigatedtheinfluenceofgasolinesulfurcontentondurabilityofcatalyticconverterforvehicleexhaustgas.Twogasolinesampleswithdifferentsulfurcontents(equatingto150μg/gand50μg/gofsulfur,respectively)wereusedtoexaminethedurabilityandperformanceofcatalyticconverteronthebenchtest.Thetestresultshaverevealedthatincomparisontotheinfluenceofsulfuronageingofcatalyticconverterthethermalageinghadamoreremarkableimpactontheperformanceofcatalyticconverter,andtheperformanceofcatalyticconvertercouldberestoredbyhigh-temperaturedesulfurizationprocessafterageingbythehigh-sulfurgasolinesample(containing150μg/gofsulfur).
简介:SelectivelyconvertingCOandH2togasolineproduct(isoparaffinandolefin)inonestepstillremainsagreatchallenge.WedemonstrateeffectiveH-USYzeolitesupportednano-cobaltbifunctionalcatalystsforthiscatalyticreaction,whicharepreparedbythenovelphysicalsputteringprocess.Particlesofthesputteredcobaltexistinnano-levelandarewell-dispersedonacidUSYzeolite.Easyactivationoftheloadednano-cobaltisalsoachievedinalow-temperaturehydrogenreductionatmosphere.Inthetandemcatalyticreaction,thesputteredbifunctionalCo/USYcatalystexhibitsamuchhigherCOconversionandhigherisoparaffinselectivitythantheconventionalimpregnatedone.ComparedwithH-Mor,H-Betaandotherzeolitessupportedcatalysts,H-USYzeolitesupportedcobaltcatalystshowstheclearestpromotionaleffectontheactivityofFischerTropschsynthesis.Thedescribedsynthesishereinprovidesanewpathwaytosolvetheproblemcausedbythestrongmetal-supportinteraction(MSI)inheterogeneouscatalysis.