简介：WeinvestigatethesurfacestructureandcompositionofaYBa2Cu3Oy(YCO)thinfilmodifiedbyCF4plasmafluorination.Inadditiontotheabsorptionofhydrocarbons,chemicalreactionsoftheYBCOsurfacetakeplaceduringCF4plasmatreatment.Variousx-rayphotoelectronspectroscopicdataarereportedanddiscussed.Theexistenceofathinbarrierisconfirmed,whichhomogeneouslycoverstheedgeofthebaseYBCOfilminourinterfaceengineeringJosephsonjunction.MeasurementsofAugerelectronspectroscopicdataandtheresistanceversustemperatureindicatethatthebarrierisacontrollable-insulatinglayer.
简介：Two-dimensional(2D)materialshaveattractedgreatresearchinterestsduetotheiruniqueproperties.2DMoS2,unlikeitsbulkformwhichwidelyusedassolidlubricantandcatalyst,isofbrilliantapplicationprospectinnanoelectronicsandoptoelectrnics.Theelectronicdevicesworkinkindsofradiationenvironment.Toevaluatetheionradiationeffectsonmaterialpropertiesandstabilityofdevice,theswiftheavyionradiationeffectonsingle-layerMoS2wasstudiedinthiswork[1??2].
简介：通过5-甲基-7-甲氧基异黄酮与盐酸羟胺的缩合制得中间产物4-苯基-5-（2-羟基-4-甲氧基-6-甲基苯基）异恶唑,然后经过光异构化反应合成了4-甲氧基-6-甲基-7a-苯基苯并吡喃并[2,3-b]氮丙啶-7-酮,并采用IR,NMR,HRMS和单晶X-衍射分析对其结构进行了表征.单晶X-衍射分析结果表明：标题化合物属于单斜晶系,空间群P2（1）/n.在其晶体结构中,存在着氢键及芳香堆积作用,这些作用将标题化合物分子组装成了三维网络结构.
简介：
简介：IncorporationofstrontiumintoV-Moalumina-supportedcatalystenhanceditsperformance(increasedconversionandselectivity,decreasedreducibilityandimprovedstability)inpropaneoxydehydrogenationtopropylene.12.5%SrloadingwasshowntobetheoptimumcontenttotheV-Mocatalyst.Theresultsweresupportedbyvariouscharacterizationtechniques,namely,BET,XRD,SEM,FTIRandTPD.
简介：与黄金和氧化铁nanoparticles并且与silibinin装载的PEGylated-PLGA随机的nanofibrous膜被electrospinning免职准备。nanofibrous膜能遥远地被控制并且由一盏激光灯或磁场激活在需求上释放生物代理人。nanosystems用扫描电子显微镜学被描绘，红外线的光谱学，原子磁性的回声光谱学，和thermogravimetric分析的Fourier变换。装载效率和药内容百分比的药被紫外力的光吸收光谱学决定。nanofibrous膜由相对低紧张的激光照耀或由一个磁场刺激了为至少60h显示出持续silibinin版本，没有爆炸效果。建议便宜electrospinning过程能够集合，经由一个一步舞过程，有外部地为控制的药交货要激活的金属性的nanoparticles的刺激应答的装载药的nanosystem。
简介：Pd-containingionicliquid（IL）1-hexyl-3-methylimidazoliumtetrafluoroborate（C6MIMBF4）immobilizedon7-Al2O3（Pd-IL/γ-Al2O3）waspreparedandcharacterizedbyFouriertransforminfraredspectroscopy（FTIR）,scanningelectronmicroscopy（SEM）andBrunauer-Emmett-Teller（BET）analysis.TheinfluencesofC6MIMBF4loadingandPdonmethaneconversiontoC2hydrocarbonsundercoldplasmawereinvestigated.FTIRandSEManalysesindicatedthatC6MIMBF4hadbeensuccessfullyimmobilizedon7-Al2O3andtheC6MIMBF4showedexcellentstabilityundercoldplasma.TheresultsofBETandmethaneconversionshowedthatwiththeincreaseinimmobilizationamountofC6MIMBF4ontoγ-Al2O3,thespecificsurfaceareaandporevolumeofIL/γ-Al2O3decreased,whiletheselectivityandyieldofC2hydrocarbonsincreased.TheselectivityofC2hydrocarbonswas94.6%whentheloadingofC6MIMBF4was40%,andthepercentageofC2H4inC2hydrocarbonswasashighas64%whenusingPd-IL/γ-Al2O3asacatalystwithnoconventionalthermalreductiontreatment.Opticalemissionspectra（OES）fromthecoldplasmareactorduringmethaneconversionwerealsostudied.TheresultsindicatedthattheintensityoftheC2,CH,H,andCactivespeciesfrommethaneandhydrogendecompositionincreasedwhenIL/γ-Al2O3orPd-IL/γ-Al2O3wasintroducedintotheplasmasystem.BasedontheanalysesofthegasproductandOESspectra,itcanbeconcludedthatthesurfacecatalyzedreactionsbetweenplasmaandionicliquidwereveryimportantforthereductionofPd2+andtheformationofC2H4.
简介：Inthecurrentpaper,dry(CO2)-reformingofglycerol,anewreformingroute,wascarriedoutoveralumina(Al2O3)-supported,non-promotedandlanthanum-promotednickel(Ni)catalysts.Bothsetsofcatalystsweresynthesizedviaawetco-impregnationprocedure.Physicochemicalcharacterizationofthecatalystsshowedthatthepromotedcatalystpossessedsmallermetalcrystallitesize,hencehighermetaldispersioncomparedtothevirginNi/Al2O3catalyst.ThiswasalsocorroboratedbythesurfaceimagescapturedbytheFESEManalysis.Fromtemperature-programmedcalcinationanalysis,thederivativeweightprofilesrevealedtwopeaks,whichrepresentawatereliminationpeakatatemperaturerangeof373to473Kfollowedbynickelnitratedecompositionfrom473to573K.Inaddition,BETsurfaceareameasurementsgave85.0m2g-1forthenon-promotedNicatalyst,whilstthepromotedcatalystsshowedanaverageof1%to6%improvementdependingontheLaloadings.Significantly,reactionstudiesat873KshowedthatglyceroldryreformingsuccessfullyproducedH2.The2%La-Ni/Al2O3catalyst,whichpossessedthelargestBETsurfacearea,gaveanoptimumH2generation(9.70%)ataglycerolconversionof24.5%.
简介：Nanostructuredtransitionmetaloxidesarepromisingalternativeanodesforlithiumionbatteries.Li-ionstorageperformanceisexpectedtoimproveifhighpackingdensityenergyparticlesareavailable.Herein,Mn2O3microsphereswithaca.18μmdiameterandatappeddensityof1.33g/cm3weresynthesizedbyafacilesolvothermal-thermalcoversionroute.SphericalMnCO3precursorswereobtainedthroughsolvothermaltreatmentandtheydecomposedandconvertedintoMn2O3microspheresatanannealingtemperatureof700C.TheMn2O3microspheresconsistedofMn2O3nanoparticleswithanaverage40nmdiameter.TheseporousMn2O3microspheresallowgoodelectrolytepenetrationandprovideanionbufferreservoirtoensureaconstantelectrolytesupply.TheMn2O3microsphereshavereversiblecapacitiesof590and320mAh/gat50and400mA/g,respectively.Wethusreportanefficientrouteforthefabricationofenergyparticlesforadvancedenergystorage.
简介：TheeffectsofSO2,SO3ondenovosynthesisofpolychlorinateddibenzo-p-dioxins(PCDDs)anddibenzofurans(PCDFs)werestudiedusingmodelflyashesincorporatingcopperoxideandactivatedcarbon.ItwasfoundthattheinhibitiveeffectofSO2onPCDD/FsformationissimilartothatofSO3.Toinvestigatetheinhibitionmechanism,CuSO4formationsfrombothCuOandCuCl2wereexamined.TheabilityofSO3toconvertCuCl2andCuOonasilicasupportintosulfateismuchstrongerthanthatofSO2.However,replacingsilicabyactivatedcarbonleadstoamuchhighconversionofCuCl2toCuSO4inthepresenceofSO2.ThepromotionbyactivatedcarbonisexplainedbythereductionofCuCl2toCu2Cl2andtheeventualconversionofCu2Cl2intoCuSO4isthemaininhibitionmechanismofSO2ondenovosynthesisofPCDD/Fs.
简介：
简介：采用铜（Ⅱ）盐和3,5-二氯水杨醛缩丝氨酸以及4,4′-联吡啶在乙醇水溶液中合成了具有二维层状的配位聚合物.通过元素分析、红外光谱对该配位聚合物进行了表征,并利用X射线单晶衍射仪对其结构进行了鉴定.晶体结构表明,该标题配合物属三斜方晶系,空间群C2/c,晶胞参数为a=2.711（3）nm,b=2.711（3）nm,c=4.977（5）nm;α=90.00°,β=90.00°,γ=120.00°,V=3.1678nm^3,Z=18,Dc=1.173g·cm^-3,F（000）=11448,μ=0.807mm-1,R1=0.0788,wR2=0.1872.
简介：Anovelflower-likehydratedmagnesiumcarbonatehydroxide,Mg_5(CO_3)_4(OH)_2·4H_2O,withmicro-structurecomposedofindividualthinnano-sheetswassynthesizedusingafacilesolutionroutewithouttheuseoftemplateororganicsurfactant.Reactiontimehasanimportanteffectonthefinalmorphologyoftheproduct.Themicro-structureandmorphologyofMg_5(CO_3)_4(OH)_2·4H_2OwerecharacterizedbymeansofX-raydiffractometry(XRD),field-emissionscanningelectronmicroscopy(FE-SEM).Brunauer-Emmett-Teller(BET)surfaceareasofthesampleswerealsomeasured.Theprobableformationmechanismofflower-likemicro-structurewasdiscussed.ItwasfoundthatMg_5(CO_3)_4(OH)_2·4H_2Owithflower-likemicro-structurewasanovelandefficientcatalystforthesynthesisofdiphenylcarbonate(DPC)bytransesterificationofdimethylcarbonate(DMC)withphenol.
简介：AnovelSr2CuInO3Soxysulfidep-typesemiconductorphotocatalysthasbeenpreparedbysolidstatereactionmethodanditexhibitsintriguingvisiblelightabsorptionpropertieswithabandgapof2.3eV.Thep-typesemiconductorcharacterofthesynthesizedSr2CuInO3SwasconfirmedbyHallefficientmeasurementandMott-Schottkyplotanalysis.First-principlesdensityfunctionaltheorycalculations(DFT)andelectrochemicalmeasurementswereperformedtoelucidatetheelectronicstructureandtheenergybandlocations.Itwasfoundthattheas-synthesizedSr2CuInO3Sphotocatalysthasappreciateconductionandvalencebandpositionsforhydrogenandoxygenevolution,respectively.Photocatalytichydrogenproductionexperimentsunderavisiblelightirradiation(λ>420nm)werecarriedoutbyloadingdifferentmetalandmetal-likecocatalystsonSr2CuInO3SandRhwasfoundtobethebestoneamongthetestedones.
简介：One-potachievementofethyllevulinatefromcassavawasconductedinethanol-watersystemoverseveralsimplesulfatesaltcatalysts.Al2（SO4）3catalysthadthebestperformanceinsynthesizingethyllevulinatecomparingwiththoseofaseriesofsulfatesalts.Thehighestyieldsofethyllevulinatewasupto39.27%aswellas7.78%levulinateacidwhencassavawascatalyzedinethanolmediumbyadding10wt%water.13Cand1HNMRspectroscopicinvestigationsconfirmedthatisomerizationofglucosetofructoseoverAl2（SO4）3catalystisanimportantstepinproducingethyllevulinateandlevulinateacid.DuetoaggregationsofAl3+underhydrothermalconditions,tinyamountofAl3+weredetectedinfiltrateatthepercentageof0.32%evenifinabsolutewater.BronstedandLewisacidscouldimprovetheyieldofethyllevulinateandlevulinateacidbysynergisticeffect.AllresultssuggestedthatA12（SO4）3wasasimpleandefficientcatalystforethyllevulinateandlevulinateacidproduction.
客服QQ：30444492琼网文【2021】1550-113号
增值电信业务经营许可证：琼B2-20210322
出版物经营许可证：新出发龙华出字第(2021)009号
广播电视节目制作经营许可证：(琼)字第00779号
版权所有 ©2002-2025 期刊网(www.qikanchina.com) 琼ICP备2021005105号
![氨基酸功能化多钼酸盐[（Gly）<b style='color:red'>2</b>（H<b style='color:red'>2</b>O）<b style='color:red'>2</b>Cu]K<b style='color:red'>3</b>[Al（OH）6Mo6O18]·7H<b style='color:red'>2</b>O的合成及表征](/image/thesis2 "氨基酸功能化多钼酸盐[（Gly）<b style='color:red'>2</b>（H<b style='color:red'>2</b>O）<b style='color:red'>2</b>Cu]K<b style='color:red'>3</b>[Al（OH）6Mo6O18]·7H<b style='color:red'>2</b>O的合成及表征")
![4-甲氧基-6-甲基-7a-<b style='color:red'>苯基</b>苯并吡喃并[<b style='color:red'>2</b>,3-b]氮丙啶-7-酮的合成及晶体结构研究](/image/thesis3 "4-甲氧基-6-甲基-7a-<b style='color:red'>苯基</b>苯并吡喃并[<b style='color:red'>2</b>,3-b]氮丙啶-7-酮的合成及晶体结构研究")
![[Co（1,10-phen）（H<b style='color:red'>2</b>O）（VO<b style='color:red'>3</b>）<b style='color:red'>2</b>]的水热合成、结构及电化学性质](/image/thesis4 "[Co（1,10-phen）（H<b style='color:red'>2</b>O）（VO<b style='color:red'>3</b>）<b style='color:red'>2</b>]的水热合成、结构及电化学性质")
![一个新的二维配位聚合物：{Cu<b style='color:red'>2</b>[C10H8Cl<b style='color:red'>2</b>NO4]<b style='color:red'>2</b>[C10H8N<b style='color:red'>2</b>]<b style='color:red'>3</b>}n的合成及其晶体结构](/image/thesis13 "一个新的二维配位聚合物：{Cu<b style='color:red'>2</b>[C10H8Cl<b style='color:red'>2</b>NO4]<b style='color:red'>2</b>[C10H8N<b style='color:red'>2</b>]<b style='color:red'>3</b>}n的合成及其晶体结构")
![Efficient Synthesis of <b style='color:red'>3</b>,5,6,8-Tetrahydro-4H-thiopyrano[4＇,<b style='color:red'>3</b>＇：4,5]. thieno｜<b style='color:red'>2</b>,3-d]pyrimidin-4-ones via an Iminophosphorane](/image/thesis14 "Efficient Synthesis of <b style='color:red'>3</b>,5,6,8-Tetrahydro-4H-thiopyrano[4＇,<b style='color:red'>3</b>＇：4,5]. thieno｜<b style='color:red'>2</b>,3-d]pyrimidin-4-ones via an Iminophosphorane")
