简介:Whitelight-emittingYVO_4:1mol.%Dy~(3+),xmol.%Eu~(3+)phosphorpowderswithordermorphologyandwellcrystallizationwerehydrothermallysynthesizedat180°C.Themicrostructure,white-lightemission,andlight-emittingmechanismofthepowderswerecarefullystudiedusingX-raydiffractometry,scanningelectronmicroscopyandphotoluminescencespectra.TheexcitationandemissionspectraofthephosphorpowdersindicatedthecoexistenceofefficientenergytransferfromEu~(3+)toDy~(3+)andinefficientenergytransferfromDy~(3+)toEu~(3+)besidestheenergytransferfromVO_4~(3–)toEu~(3+).IncreasingtheEu~(~(3+))concentrationinitiallyenhancedandthenweakenedtheluminescentintensityofDy~(3+).Thewhite-lightemissionsofYVO_4:1mol.%Dy~(3+),xmol.%Eu~(3+)phosphorpowderswerebothrelatedtotheenergytransferbetweenVO_4~(3–)andDy~(3+)/Eu~(3+),aswellasbetweenEu~(3+)andDy~(3+).TheinefficientenergytransferfromDy~(3+)toEu~(3+)wasfirstfound.
简介:以六水合硝酸钴(Co(NO3)2·6H2O)和硫脲为原料,采用混合溶剂热法制备硫化钴(COS)纳米晶。利用X射线衍射(XRD),扫描电镜(SEM)和透射电镜(TEM)对硫化钴纳米晶的组成、粒径及表面形貌进行表征。结果表明,在180℃恒温条件下所得粉末样品为六方相CoS纳米粉末,粉末粒径在40nln左右。粉末的产率随温度升高而增大,当反应温度上升到180℃时产率接近60‰温度进一步升高到200℃时产率基本不变,但晶粒异常长大。加入分散剂PEG能有效控制粉末颗粒的尺寸并抑制粉末的团聚;此外,减少有机溶剂EG的含量可获得更高结晶度的CoS纳米晶,但由于反应速率过快,不利于控制粉末的粒径。
简介:采用选择性激光熔覆法,在基板温度分别为100,150,和200℃条件下制备M2粉末高速钢合金,分析基板温度对合金组织结构与力学性能的影响。结果表明,基板温度升高有利于提高M2粉末高速钢的致密度和整体组织的均匀性。当基板温度为200℃时,高速钢组织均匀致密,各元素固溶程度高,且碳化物含量高,组织中柱状晶不再沿Z轴方向单一生长,同时合金的显微硬度(HV0.1)达到最高,HV0.1为1150,相比基板温度为100℃时的合金提高近40%。随基板温度从100℃升高到200℃,沿Z轴打印的M2高速钢室温抗拉强度从865.23MPa降低到443.85MPa,主要原因是合金中单一方向的柱状晶数量减少。
简介:Eu-activatedCaMoO4phosphorswereco-precipitatedinanaqueoussolution,andNH3·H2O,NH4HCO3and(NH2)2COaspre-cipitatingaidagentswerecomparedbasedonthemorphologyandparticlesizedistributionofthephosphorsamples.Sm3+assensitizerionwasinvestigatedontheluminescenceofCaMoO4:Eu,anditcouldstrengthenthe406nmabsorptionofthisphosphor.Atlast,thescheeliteCaMoO4:EuandwolframiteZnMoO4:Euwereselectedtocomparetheirhostabsorption.TheresultshowedthatthescheelitemolybdatehostexhibitedstrongerUVabsorptionthanwolframiteone.
简介:Thecoilingtemperatureofthehotstriprollingprocessplaysanimportantroleinstripqualitycontrol.Thenewly-builtlaminarflowcoolingcontrolsystemwasindependentlydevelopedbyBaosteel.L2conductstotallydynamiccontrol(L1onlyexecutestheresultfromL2,anddoesnotconductanydynamiccontrol).Thesystemhasmanyadvantages,suchasquickreal-timecontrol,accuratemodelcalculation,quickresponseafterself-adaptation,etc.Comparedwiththe2050mmhotstriprollingline,thenewsystemcansatisfythestrictcoolingrequirementsofhighstrengthsteel,siliconsteelandheavyplatesbecauseofitsnewly-developedtechnologiesofcoolingratecontrol,stripcoolingbysectionsandproportion-integral-differentialcoefficient(PID)feedbackfuzzycontrol.
简介:AseriesofMn-basedcatalysts,MnOx,MnOx-CeO2,Pd-Mn-Ce,MnOx/ACwereprepared.AndtheirperformancesforNOlow-temperatureSCRwereinvestigatedinthisstudy.TheNOconversionisabout90%at100℃onMnOx-CeO2andalmostallNOcanbeconvertedat120℃.SimilarresultsarealsoobservedinthetestsonMnOx-CeO2/AC.Theexcellentlow-temperaturecatalyticactivityofmodifiedMn-basedcatalysts,whichmaybemainlyduetotheoxygenstoragefunctionofCeO2,canimprovetheoxygenflowonthecatalystssurface.ThentheoxidationofNOtoNO2isaccelerated,whichisthekeystepofNOSCR.
简介:ThedopedZnOnanorodsasaphotocatalystwithdifferentEucontentswerepreparedbymicrowaveassistedmethodandtheywerecharacterizedbymeansofX-raydiffraction(XRD),energy-dispersiveX-rayspectroscopy(EDS),UV-Visspectroscopy,surfaceareaBrunauer-Emmett-Teller(BET),X-rayphotoelectronspectroscopy(XPS),scanningelectronmicroscopy(SEM)andtransmissionelectronmicroscopy(TEM).TheaveragecrystallitesizeandbandgapenergyofEu-dopedZnOwerevariedwiththeEucontent.TheXRDpatternofEu-dopedZnOindicatedhexagonalcrystalstructurewithanaveragecrystallitesizeof25nm.ThepresenceofeuropiumwithtrivalentstateanditsdopingsuccessfullyintothecrystallatticeofZnOmatrixwereconfirmedbyXPStechnique.ThephotocatalyticactivityofEu-dopedZnOnanorodswasevaluatedformethylorangedegradation.Thephotocatalyticexperimentsshowed~91%degradationofmethylorangeover0.2mol.%EudopedZnOsamplewithin3hunderUVlight(365nm).