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.

简介：Arylhalidesareakindofextremelyvaluablecompoundsusedintransition-metal-catalyzedcouplingreactions,aswellasimportantstructuremotifsinmanynaturalproductsandmanufactureddrugs[1,2].Theclassicalapproachforpreparationofhaloarenesiselectrophilicaromaticsubstitution(EAS)usingvarioushalogenatingreagentsoroxidativehalogenationswithhalogenatingreagentgeneratedinsitufromhalidesandoxidants,suchasperoxide,oxygenandmeta-cholorperoxybenzoicacid(mCPBA)[3,4].However,harshreactionconditionsarerequiredforhalogenationoflessactivearomatics.orthoMetalationfollowedbyhalogenquenchingisanotherapproachforhalogenationofaromatics[5].However,thereareobviousdrawbacksforthesemethods,suchaslowregioselectivity,harshconditionsandevendangerousprocedures.Therefore,thedevelopmentofanalternativeandpracticalwayremainschallengeinorganicsynthesis.

简介：Theroleofpulseparametersonnanoparticlepropertyisinvestigatedself-consistentlybasedonacoupleoffluidmodelandaerosoldynamicsmodelinacapacitivelycoupledparallel-plateacetylene(C2H2)discharge.Inthismodel,themasscontinuityequation,momentumbalanceequation,andenergybalanceequationforneutralgasaretakenintoaccount.Thus,thethermophoreticforceariseswhenagastemperaturegradientexists.Thetypicalresultsofthismodelarepositiveandnegativeiondensities,electronimpactcollisionsrates,nanoparticledensity,andchargedistributions.Thesimulationisperformedfordutyratio0.4/0.7/1.0,aswellaspulsemodulationfrequencyfrom40kHzto2.7MHzforpureC2H2dischargesatapressureof500mTorr.Wefindthatthepulseparameters,especiallythedutyratio,haveagreataffectonthedissociativeattachmentcoefficientandthenegativedensity.Moreimportantly,bydecreasingthedutyratio,nanoparticlesstarttodiffusetothewall.Undertheactionofgasflow,nanoparticledensitypeakiscreatedinfrontofthepulseelectrode,wherethegastemperatureissmaller.

简介：

简介：Forsyngasproduction,thecombustionoffossilfuelsproduceslargeamountsofCO2asagreenhousegasannuallywhichintensifiesglobalwarming.Inthisstudy,chemicalloopingcombustion(CLC)hasbeenutilizedfortheeliminationofCO2emissiontoatmosphereduringsimultaneoussyngasproductionwithdifferentH2/COratioinsteamreformingofmethane(SR)anddryreformingofmethane(DR)inaCLC-SR-DRconfiguration.InCLC-SR-DRwith184reformertubes(similartoanindustrialscalesteamreformerinZagrosPetrochemicalCompany,Assaluyeh,Iran),DRreactionoccursoverRh-basedcatalystsin31tubes.Also,SRreactionishappenedoverNi-basedcatalystsin153tubes.CLCviaemploymentofMn-basedoxygencarrierssuppliesheatforDRandSRreactionsandproducesCO2andH2Oasrawmaterialssimultaneously.AsteadystateheterogeneouscatalyticreactionmodelisappliedtoanalyzetheperformanceandapplicabilityoftheproposedCLC-SR-DRconfiguration.Simulationresultsshowthatcombustionefficiencyreached1attheoutletoffuelreactor(FR).Therefore,pureCO2andH2OcanberecycledtoDRandSRsides,respectively.Also,CH4conversionreached0.2803and0.7275attheoutletofSRandDRsides,respectively.Simulationresultsindicatethat,3223kmolh-1syngaswithaH2/COratioequalto9.826wasproducedinSRsideofCLC-SR-DR.Afterthat,1844kmolh-1syngaswithaH2/COratioequalto0.986wasachievedinDRsideofCLC-SR-DR.ResultsillustratethatbyincreasingthenumberofDRtubesto50tubesandconsidering184fixedtotaltubesinCLC-SR-DR,CH4conversionsinSRandDRsidesdecreased2.69%and3.31%,respectively.However,thissubjectcausedtotalsyngasproductioninSRandDRsides(inallof184tubes)enhanceto5427kmolh-1.Finally,thermalandmolarbehaviorsoftheproposedconfigurationdemonstratethatCLC-SR-DRisapplicableforsimultaneoussyngasproductionwithhighandlowH2/COratiosinanenvironmentalfriendlyprocess.

简介：对制造的单mesa终端4H-SiCPIN二极管,采用数值仿真和测试结果比对的方法,分析了各向异性迁移率效应对4H-SiCPIN二极管正向直流特性的影响。详细阐述了器件的正向直流仿真物理模型和参数选取,其中,迁移率的各向异性关系是在各向同性迁移率模型的基础上引入的,载流子寿命采用空间赋值的方法代入模型进行计算。对比结果显示,采用各向同性迁移率模型的仿真结果与实验值偏差较大,对迁移率模型进行各向异性修正后,仿真结果与实验结果符合得较好。研究表明,实际制造的4H-SiCPIN二极管在直流开态下,存在迁移率的各向异性效应。

简介：Theoccurrencemodesofalkaliandalkaline-earthmetals(AAEMs)incoalrelatetotheirreleasebehaviorandashformationduringcombustion.TobetterunderstandthetransformationofAAEMs,thereleasebehaviorofwater-soluble,HCl-soluble,HCl-insolubleAAEMsduringShenmucoal(SMcoal)oxy-fuelcombustioninthepresenceofSO2andH2Oinadrop-tubereactorwasinvestigatedthroughserialdissolutionusingH2OandHClsolutions.TheresultsshowthatthereleaseratesofAAEMsincreasewithanincreaseintemperatureunderthethreeatmospheresstudied.ThehighreleaseratesofMgandCafromSMcoalaredependentonthehighcontentofsolubleMgandCainSMcoal.SO2inhibitsthereleaseratesofAAEMs,whileH2Opromotesthem.TheeffectsofSO2andH2OontheNaandKspeciesaremoreevidentthanthoseonMgandCaspecies.AllthreetypesofAAEMsincoalcanvolatilizeinthegasphaseduringcoalcombustion.TheW-typeAAEMsreleaseexcessively,whereasthereleaseratesofI-typeAAEMsarerelativelylower.DifferenttypesofAAEMmayinterconvertthroughdifferentpathwaysundercertainconditions.BothSO2andH2Opromotethetransformationreactions.TheeffectofSO2wasrelatedtosulfateformationandthepromotionbyH2OoccursbecauseofadecreaseinthemeltingpointofthesolidaswellasthereactionofH2O.

简介：Theresultsonadissociationbehaviorofpropanehydratespreparedfrom'drywater'andcontainedunreactedresidualwaterintheformoficeinclusionsorsupercooledliquidwater(watersolutionofgas)werepresentedfortemperaturesbelow273K.Thetemperaturerampingorpressurereleasemethodwasusedforthedissociationofpropanehydratesamples.Itwasfoundthatthemechanismofgashydratedissociationattemperaturesbelow273Kdependedonthephasestateofunreactedwaterinthehydratesample.Gashydratesdissociatedintoiceandgasiftheiceinclusionswereinthehydratesample.Thesamplesofpropanehydrateswithinclusionsofunreactedsupercooledwateronly(withouticeinclusions)dissociatedintosupercooledwaterandgasbelowthepressureofthesupercooledwater-hydrate-gasmetastableequilibrium.

简介：标题化合物（C24H16N4S）以噻吩-2-甲醛、苯甲酰乙腈和3-甲基-1-苯基-1H-吡唑-5-胺为原料,在离子液体[bmim]Br溶剂中,在80℃搅拌合成得到.其结构通过单晶X射线衍射法确定,晶体属于三斜晶系,空间群P-1,相对分子质量Mr=392.47,晶胞参数a=0.93612（8）nm,b=1.03063（12）nm,c=1.16624（16）nm,V=0.96853（19）nm3,Z=2,晶胞密度Dc=1.346g/cm3,吸收系数μ=0.185mm-1,单胞中电子的数目F（000）=408.晶体结构用直接法解出,经全矩阵最小二乘法对原子参数进行修正,最终的偏离因子R=0.0585,wR=0.1337.在晶体结构中新形成的吡啶环与吡唑环近似于共平面结构.

简介：标题化合物C26H26O5以2,3-萘二甲醛和5-甲基-1,3-环己二酮为原料,在醋酸溶剂中,室温下经搅拌多组分一锅法合成得到.其结构通过单晶X-射线衍射法确定,晶体属单斜晶系,空间群P21,相对分子质量Mr=418.47,晶胞参数a=0.99004（8）nm,b=1.09098（9）nm,c=1.04246（11）nm,V=1.08753（17）nm3,Z=2,晶胞密度Dc=1.278g/cm3,吸收系数μ=0.088mm-1,单胞中电子的数目F（000）=444.晶体结构用直接法解出,经全矩阵最小二乘法对原子参数进行修正,最终的偏离因子为R1=0.0533,wR2=0.1293.在晶体结构中新形成的吡喃环为半椅式构象,而茚中五元环则为信封式构象.