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简介:TheCe-Fe-OmixedoxidewitharatioofCe/Fe=7:3,whichwaspreparedbycoprecipitationmethodandemployedasoxygencarrier,fordirectpartialoxidationofmethanetosyngasintheabsenceofgaseousoxygenwasexplored.ThemixedoxidewascharacterizedbyX-raydiffraction(XRD),X-rayphotoelectronspectroscopy(XPS)andscanningelectronmicroscopy(SEM),andthecatalyticperformanceswerestudiedinafixed-bedquartzreactorandathermogravimetricreactor,respectively.Approximately99.4%H2se...
简介:黄磷(Bi1-xSmx)2ZnB2O7(x=0.01,0.03,0.05,0.07,和0.09)被常规稳固的州的反应综合。所有样品的纯净被X光检查粉末衍射(XRD)检查。XRD分析证明所有这些混合物具有Bi2ZnB2O7的一个单个阶段,显示在Bi2ZnB2O7的双性人(3+)能被没有晶体结构的变化的Sm(3+)部分代替。在房间温度的刺激和排放系列显示出Sm(3+)的典型4f-4f转变。主导的刺激线在404nm附近由于(6)H5/2→(4)K11/2和排放光谱在563,599,646,和704nm由一系列线组成由于(4)G5/2→(6)H5/2,(6)H7/2,(6)H9/2,并且(6)H11/2分别地。在Bi2ZnB2O7的Sm(3+)的最佳的集中关于3mol%(相对1mol双性人(3+))并且批评距离Rc作为2.1nm被计算。Bi1.94Sm0.06ZnB2O7的排放紧张的温度依赖在在100和450K之间的温度范围被检验。紧张下降了到起始的紧张的一半的熄灭的温度是280K。为在Bi1.94Sm0.06ZnB2O7的Sm(3+)的一生作为0.29和1.03ms的价值被适合。
简介:LuminescencelifetimeofCe(Ⅲ)forCe0.9RE0.1P5O14,whereREdenotesrareearthionsotherthanCe(Ⅲ),wasmeasuredbymeansofthetime-correlatedsinglephotoncountingtechnique.Ithasbeenfoundthatthelifetimedataarecapableofelucidatingtheenhancementorquenchingofcerium(Ⅲ)luminescencebyalienREions(otherthanCe)indoublydopedceriumpentaphosphatecrystal.
简介:StudyonMorphologyofSurfaceofLargeAreaYBCOThinFilmsonZr(Y)O2SubstrateWangRuikun(王瑞坤),SunLihong(孙丽虹),LiuHongfei(刘鸿飞)WangXiaopi?..
简介:采用高温固相法合成尖晶石LiMn2O4,并以化学沉积方式对其进行包覆氧化钴的表面处理。通过X射线衍射(XRD)、扫描电镜(SEM)等技术对表面处理前后的LiMn2O4进行表征,分析了表面处理后LiMn2O4物理特性的变化,并结合电化学性能测试,研究了表面处理及其工艺和条件对LiMn2O4电化学容量与循环性能的影响。结果表明,表面处理后LiMn2O4循环性能显著提高。随氧化物含量的增加,循环性能提高,容量降低。未经表面包覆的LiMn2O4首次充放电容量为108.13mAh/g,50次循环充放电后容量衰减26.3%。500℃加热处理的表面包覆0.5%、2%氧化钴的LiMn2O4首次循环放电容量各为118.38mAh/g、115mAh/g,经过50次充放电循环后,容量分别降低8%、7%。
简介:Thenanosizedparticlematerialsofdoped-TiO2withY2O3werepreparedbymeansofsol-geltechniqueforuseinelectrorheological(ER)fluids,andtheircrystalstructuresweremeasuredbyX-raydiffraction(XRD)analysis.TocomparewiththepureTiO2,adistinctenhancementintheshearstressunderdcelectricfieldwasfoundbyusingsuchmaterials.Thiscanbeexplainedbytheincreaseofthedielectriclossanddielectricconstantatlowfrequency.TheeffectsofthecrystalstructureoftheparticlesonthedielectricpropertyandERperformanceofmaterialswereinvestigated.
简介:ThemorphologyandcorrosionbehaviorofNi/Al2O3compositecoatingspreparedusingdouble-pulsedelectrodepositingtechniqueafteroxidizedunder800℃NaCldepositinairenvironmentwereanalyzedbyscanningelectricalmicroscope(SEM),X-raydiffraction(XRD)andenergydispersivespectrum(EDS).TheresultsshowedthatthecorrosionofallcompositecoatingswasacceleratedunderNaCldeposits,andthecorrosionproductswereratherporouswithpooradherencetothematrix.Al2O3particlesinthecoatingscanrefinethegrainsizeandimprovethehightemperaturecorrosionresistanceofthecoatings.Withinthetestscope,themoreAl2O3particlesinthecoatings,thelowercorrosionratescouldbeobtained,andthecorrosionmechanismwasalsodiscussed.
简介:SinglephaseofBa1-xMgAl10O17:xEu2+(0.02≤x≤0.14)phosphorswasfirstsuccessfullypreparedbyco-precipitationinaqueousmediumwitha'reversestrike'method,usingoxalicacidandammoniatogetherasprecipitants.Completelycrystallizedphosphorswereobtainedat1300℃,whichis300℃lowerthanthetemperatureofsolid-statereaction.TheirphotoluminescencewasinvestigatedunderUVandVUVregion,respectively.TheemissionspectraofBa1-xMgAl10O17:xEu2+samplesexcitedby254or147nmshowedacharacteristicwidebandwiththepeakcentredatabout450~454nm.Optimumemissionintensityreachedatx=0.1andthenconcentrationquenchingoccurred.Thesynthesizedphosphorshows10%higheremissionintensitythanthatpreparedbysolid-statereaction.
简介:AseriesofCe-Fe-Zr-O(x)/MgO(xdenotesthemassfractionofCe-Fe-Zr-O,x=10%,15%,20%,25%,30%)complexoxideoxygencarriersforselectiveoxidationofmethanetosynthesisgaswerepreparedbytheco-precipitationmethod.ThecatalystswerecharacterizedbymeansofX-raydiffractionandH2-TPR.TheXRDmeasurementsshowedthatMgFeO4particleswereformedandFe2O3particleswelldispersedontheoxygencarriers.Thereactionsbetweenmethanedilutedbyargon(10%CH4)andoxygencarrierswereinvestigated.SuitablecontentofCeO2/Fe2O3/ZrO2mixedoxidescouldpromotethereactionbetweenmethaneandoxygencarriers.Therearemainlytwokindsofoxygenofcarriers:surfacelatticeoxygenwhichhadhigheractivitybutlowerselectivity,andbulklatticeoxygenwhichhadloweractivitybuthigherselectivity.Amongallthecatalysts,Ce-Fe-Zr-O(20%)/MgOexhibitedthebestcatalyticperformance.Theconversionofthemethanewasabove56%,andtheselectivityoftheH2andCOwerebothabove93%,theratioofH2/COwasstableandapproachedto2foralongtime.
简介:Loadedonthecordierite,therareearthdopedcompositecatalystwaspreparedbysol-gelmethodcombinedwithdippingtechnique.TakingOrthodichlorobenzeneasmodel,thecatalystwasusedtoremovethedioxinsofthewastegas.Theresultsshowedthatat280℃andgasspacevelocitybeing8000h-1,theorthodichlorobenzenecouldberemovedeffectivilybythepreparedCeO2-TiO2-V2O5compositecatalystwhoseactivitywasremarkablyenhancedbythedopingofCe,whiletheindustrialside-streamtestofdioxinsfromrefuseincinerationsmokeindicatedthatthedecompositionratecouldreachabove93%underthesameconditions.
简介:VariousaffectingfactorsanddegradationmechanismwerestudiedonultrasonicdegradationofmethylorangeadoptingY2O3dopinganataseTiO2catalystpreparedinlaboratory.Intheexperiment,theUV-VISspectrophotometerwasusedtofollowandinspectthedegradationprocessofmethylorange.TheresultsindicatethattheultrasonicdegradationratiosofmethylorangeinthepresenceofanataseTiO2catalystaremuchbetterthanthosewithoutcatalyst.Moreover,thecatalyticperformanceofY2O3dopinganataseTiO2catalystisobviouslyhigherthanthatofanataseTiO2catalystwithoutdoping.TheoptimalconditionswereadoptedinthisworkandthedegradationandCODeliminationratioofmethylorangegotto98%and99.0%in90min,respectively.
简介:ThephotocatalystsK4Nb6017andK4Nb6017dopedwithFe^3+andCr^3+werepreparedbysolidstatereactionandwerecharacterizedbypowderx-raydiffraction,UV-visdiffusivereflectanceandscanningelectronmicroscopy.ThephotocatalyticactivityofK4Nb6O17andK4Nb6O17dopedwithFe^3+,Cr^3+wereinvestigatedwithmethanolaselectrondonorandPtaspromotercatalystunder+400nmUVirradiation.Thedifferenceofphotocatalyticactivitybetweenthemwasalsodiscussed.TheindividualrateofhydrogenevolutionfortheK4Nb6O17,Fe-K4Nb6O17andCr-K4Nb6O17asphotocatalystsare5.35,5.00,6.25mmol·L^-1.h^-1respectively.