简介：MgO-Al2O3-Cr2O3rammingmixesmadeofdifferentrawmaterialshavedifferentmineralstructureanddifferentphysicalpropertiesthoughwiththeidenticalparticlesizedistribution,thesameamountofbinderandchemicalcomposition.Theresidualcarboncontentofthefusedmagnesia-chromematerialmadeinreducingatmosphereisveryhigh,ifthismaterialsisusedintheMgO-Al2O3-Cr2O3rammingmix,itwouldcausespallingofthefurnaceliningduringdrying-out.
简介：AseriesofmesoporousCu-Mn-Al2O3(CMA)materialswassynthesizedatmoderatetemperatureandtheirstructureswerecharacterizedbyXRD,N2physicaladsorptionandTPRtechniques.Itwasfoundthatusingmetalcomplexion[Cu(NH3)42+-Mn(NH3)62+]asrawmaterialsiseasiertoformgood-structuremesoporousCu-Mn-Al2O3materialsthanusingitsnitratesalt[Cu(NO3)2-Mn(NO3)2].TheTPRtestsresultsindicatethatCuOandMnOxwerehomogeneouslydispersedinthemesoporousmaterials.TheircatalyticapplicationtopreferentialcatalyticoxidationofCOinahydrogen-richstreamwasstudied.TheactivityvariesintheorderofCMA(1:1,molarratio)>CMA(1:2)>CMA(2:1)>CMA(CP)>CMA(1:0)≈CMA(0:1).TheCMA(1:0)andCMA(0:1)haveloweractivitycomparedtoothersamples,implyingthatthereexistedcoordinationeffectbetweenCu-Mninthesamples.TheselectivityvariedintheorderofCMA(0:1)≥CMA(1:2)>CMA(1:1)>CMA(2:1)>CMA(1:0)athighertemperature(≥120°C),indicatingthatincreasingtheCucontentenhancedtheconversionofH2.ThesampleCMA(CP)madebycoprecipitationmethodhasalowerCOoxidationactivityandselectivitythanitscounter-partsofmesoporousCu-Mn-Al2O3materials[CMA(1:2)],thisattributedtothelowersurfaceareaoftheformerandpoorinteractionofCuOwithMnOx.
简介：Thesolidaddofthefirstprotonatedzincoborophosphate,(H3O)Zn(H2O)2BP2O8·H2O(1),wassoventothermallysyn-thesizedbythereactionofZn(NO3)2·6H2OandH3BO3withH3PO4inamixedsolvent,andstructurallycharacterizedbysingle-ystalX-raydiffractionanalysis.ItcrystallizesinthehexagonalP6122,a=0.9604(4)nm,c=1.5297(6)nm,V=1.2218(8)nm^3,Dc=2.921g/cm^3,Z=6,F(000)=1080,μ=3.495mm^-1.Thestmchwefeaturesthatthetetrahedra-te-trahedrahdlcesinterconnectedbyoctahedraandstronghydro-gembondinteractionsformathree-dimensionalframework.Theprotonatedwatermoleculesarelocatedatuniquepositions.othercharacterizationsbyIRandthermalanalysisarealsode-scribed.
简介：XunwuRareEarthCorporationhasintroducedP507reductionextractionprocessfromAnhuiRe-searchInstituteofMetallurgytoprepareeuropiumoxideoffluorescentgradeinonestep.Theprocesshasbeenemployedinaproductionlineinthecorpo-ration.Andafterthreemonthsindustrialexperi-ment,allthetechnicalindexesreachedthedesigned
简介：EmployingLi2CO3,NiO,Co3O4,andMnCO3powdersasstartingmaterials,Li[Ni1/3Co1/3Mn1/3]O2wassynthesizedbysolid-statereactionmethod.Variousgrindingaidswereappliedduringmillinginordertooptimizethesynthesisprocess.Aftersuccessiveheattreatmentsat650and950℃,thepreparedpowderswerecharacterizedbyX-raydiffraction(XRD)analysis,scanningelectronmicroscopy,andtransmissionelectronmicroscopy.Thepowderspreparedbyaddingsalt(NaCl)asgrindingaidexhibitaclearR3mlayerstructure.ThepowdersbyothergrindingaidslikeheptaneshowsomeimpuritypeaksintheXRDpattern.Theformerpowdersshowauniformparticlesizedistributionoflessthan1μmaveragesizewhilethelattershowsawidedistributionrangingfrom1to10μm.EnergydispersiveX-ray(EDX)analysissshowthattheratioofNi,Co,andMncontentinthepowderisapproximately1/3,1/3,and1/3,respecively.TheEDXdataindicatenoincorporationofsodiumorchlorineintothepowders.Charge-dischargetestsgaveaninitialdischargecapacityof160mAh·g-1forthepowderswithNaCladditionwhile70mAh·g-1forthepowderswithheptane.
简介：PolycrystallinesBi0.5Ca0.5–xLaxFe0.3Mn0.7O3(x=0,0.05,0.10,0.15,0.20,0.25)werepreparedbymoltensaltmethodandshowedperovskiteorthorhombicstructurewithspacegroupPnma.Themagneticmeasurementsindicatethatthecompoundsexhibitantiferromagneticbehaviorinatemperaturerangeof4―300K.ThemeasurementsoftransportpropertiessuggestthatthesubstitutionofLaforCaenhancedtheconductivity,andakinkappearedonthecurveoftemperaturedependenceofresistivityat275K,whichisrelatedtothespin-reorientationinthesamples.
简介：LongafterglowphotoluminescentmaterialsSr2MgSi2O7dopedwithEu2+,Dy3+werepreparedbysol-gelmethod.ThesynthesizedsampleswerecharacterizedbyX-raydiffraction.Theexcitationspectrum,emissionspectrumandlongdecaycurveweremeasuredandanalyzed.XRDpatternindicatesthatphosphoriswithSr2MgSi2O7crystalstructure.Thewiderangeofexcitationwavelengthindicatesthatluminescentmaterialcanbeexcitedbylightfromultravioletraytovisiblelight.Themainpeakofemissionspectrumislocatedat466nm.Sampleexcitedbyvisiblelightcanemitbrightbluelight,andtheafterglowtimelastsmorethan8h.
简介：
简介：Layeredcathodematerialsofhigh-temperaturelithiumbatteries,LiNi1/3Mn1/3Co1/3O2aresynthesizedbyasol-gelmethodwithvariationinfinalsinteringtemperatureforboreholeapplications.Thestructure,morphologyandhigh-temperaturedischargeperformanceoftheseresultingproductsareinvestigatedbyX-RayDiffraction（XRD）,scanningelectronmicroscopy（SEM）,laserparticlesizeanalysis,galvanostaticandpulsedischarge.Theresultsofstructuralanalysisindicatethatthesamplesinteredat800℃hasthecharacteristicsofgoodcrystallinity,narrowsizedistributionandlargespecificsurfaceareaatthesametime.Thedischargeexperimentsalsoindicatethatthissamplehasthebestelectrochemicalproperties,withthemaximumdischargecapacitiesof314.57and434.14mAh·g-1at200and300℃respectivelyandtheminimumcellinternalresistancesatbothtemperatures.
简介：有5-8nm的尺寸的做Eu的GaOOHnanoparticles被热水的方法作为表面活化剂用钠dodecylbenzenesulfonate(SDBS)准备。做Eu的-Ga2O3和-Ga2O3被退火进一步制作GaOOH:Eu然后由X光检查衍射(XRD)描绘了，传播电子显微镜学(TEM)和光致发光(PL)。TEM结果显示出那monodisperse做Eu3+的GaOOHnanoparticles形式然后变换进通过退火的做Eu3+的-Ga2O3和-Ga2O3GaOOH:在600和900点的Eunanoparticles?????????????????@
简介：ThecorrelationbetweenphasestructuresandsurfaceacidityofAl2O3supportscalcinedatdifferenttemperaturesandthecatalyticperformanceofNi/Al2O3catalystsintheproductionofsyntheticnaturalgas(SNG)viaCOmethanationwassystematicallyinvestigated.Aseriesof10wt%NiO/Al2O3catalystswerepreparedbytheconventionalimpregnationmethod,andthephasestructuresandsurfaceacidityofAl2O3supportswereadjustedbycalciningthecommercialγ-Al2O3atdifferenttemperatures(600–1200C).COmethanationreactionwascarriedoutinthetemperaturerangeof300–600Catdifferentweighthourlyspacevelocities(WHSV=30000and120000mL·g-1h-1)andpressures(0.1and3.0MPa).ItwasfoundthathighcalcinationtemperaturenotonlyledtothegrowthinNiparticlesize,butalsoweakenedtheinteractionbetweenNinanoparticlesandAl2O3supportsduetotherapiddecreaseofthespecificsurfaceareaandacidityofAl2O3supports.Interestingly,NicatalystssupportedonAl2O3calcinedat1200C(Ni/Al2O3-1200)exhibitedthebestcatalyticactivityforCOmethanationunderdifferentreactionconditions.LifetimereactiontestsalsoindicatedthatNi/Al2O3-1200wasthemostactiveandstablecatalystcomparedwiththeotherthreecatalysts,whosesupportswerecalcinedatlowertemperatures(600,800and1000C).ThesefindingswouldthereforebehelpfultodevelopNi/Al2O3methanationcatalystforSNGproduction.
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