简介:ThedosimetricphosphorsLi_3PO_4:M(M=Tb,Cu)wereproducedbymodifiedsolid-statemethod.ThestructuralandmorphologicalcharacterizationwascarriedoutthroughX-raydiffraction(XRD)andscanningelectronmicroscope(SEM).Additionally,thephotoluminescence(PL),thermoluminescence(TL)andopticallystimulatedluminescence(OSL)propertiesofpowderLi_3PO_4dopedwithTbandCuwerestudied.ItisadvocatedthatLi_3PO_4:CuphosphornotonlyshowshigherOSLsensitivity(25timesormore)butalsogivesfasterdecayinOSLsignalsthanthatofLi_3PO_4:Tb~(3+)phosphor.Theminimumdetectabledose(MDD)ofLi_3PO_4:M(M=Tb,Cu)phosphorsisfoundtobe21.69×10~(-3)and3.33×10~(-6)J·kg~(-1),respectively.InOSLmode,phosphorshowslineardoseresponseintherangeof0.02-20.00J·kg~(-1).InTLmode,sensitivityofLi_3PO_4:CuphosphorismorethanthatofLi_3PO_4:Tbphosphor.Thekineticsparameterssuchasactivationenergyandfrequencyfactorsweredeterminedbypeakshapemethod,andphotoionizationcrosssectionsofpreparedphosphorwerecalculated.
简介:本文介绍了低温(-50℃)乙烯球罐制造和焊接技术,制定了球罐制造工艺流程和球壳板成形工艺,通过试验确定了焊接预热温度、层间温度和后热温度,并正确选择了焊接材料。制定了乙烯球罐的焊接工艺规范,并成功地完成了低温(-50℃)乙烯球罐的制造和焊接。
简介:InordertoimprovetheelectrochemicalcyclestabilityofLa-Mg-Nisystem(PuNi3-type)hydrogenstoragealloy,NiinthealloyswaspartiallysubstitutedbyM(M=Cu,Al,Mn).AnewLa-Mg-NisystemelectrodealloysLa0.7Mg0.3Ni2.55-xCo0.45Mx(M=Cu,Al,Mn;x=0,0.1)werepreparedbycastingandrapidquenching.Theeffectsofelementsubstitutionandrapidquenchingonthemicrostructuresandelectrochemicalperformancesofthealloyswereinvestigated.TheresultsbyXRD,SEMandTEMshowthatthealloyshaveamultiphasestructure,includingthe(La,Mg)Ni3phase,theLaNi5phaseandtheLaNi2phase.Therapidquenchingandelementsubstitutionhaveanimperceptibleinfluenceonthephasecompositionsofthealloys,butbothchangethephaseabundanceofthealloys.Therapidquenchingsignificantlyimprovesthecompositionhomogeneityofthealloysandmarkedlydecreasesthegrainsizeofthealloys.TheCusubstitutionpromotestheformationofanamorphousphaseintheas-quenchedalloy,andareversalresultbytheAlsubstitution.Theelectrochemicalmeasurementindicatesthattheelementsubstitutiondecreasesthedischargecapacityofthealloys,whereasitobviouslyimprovesthecyclestabilityofthealloys.ThepositiveinfluenceofelementsubstitutiononthecyclelifeofthealloysisinsequenceAl>Cu>Mn,andnegativeinfluenceonthedischargecapacityisinsequenceAl>Mn>Cu.Therapidquenchingsignificantlyenhancesthecyclestabilityofthealloys,butitleadstoadifferentextentdecreaseofthedischargecapacityofthealloys.
简介:FluorescenceandcofluorescencepropertiesofTb(Ⅲ)solidcomplexeswerestudiedusingpyromelliticacid(PMA)asligandandfluorescenceinertionsasdopingelements.Thecofluorescenceenhancement,aresultofligandsensitizedfluorescence,wasobservedinTb(Ⅲ)solidcomplexesdopedwithfluorescentinertionsLa(Ⅲ),Gd(Ⅲ),Ca(Ⅲ),andSr(Ⅲ).Theeffectofthetypeandcontentofdopingelementsonfluorescenceenhancementwasstudied,andoptimumconditionsweredetermined.TheresultsshowthatGd(La,Ca,Sr)hasclearcofluorescenceeffectinsolidcomplexTb-M-PMAsystem,andinpresentwork,rareearthcomplexfluorescentpowderthatemitsbrightgreenfluorescenceatultravioletexcitationwasobtained,whichhadpotentialapplicationasfluorescentanti-counterfeitink.
简介:Basedonclustervariationmethod(CVM)andnaturaliterationmethod(NIM),order-disorderphasetransitionintheintercalationcompoundsM1/2TiS2issimulatedbycomputer.Thefavorableconditions,underwhich3a0×a0superstructureisformed,aregiven,andtheresultsareingoodagreementwiththeexperimentsandtheoreticalcalculations.TherelationshipbetweencriticaltemperatureandM-ion-vacancyinteractionparameterislinear.
简介:1IntroductionTherareearthcobaltalloyshavethepotentialformakingthemagneticandmagnetoopticalmaterials.Sofar,therareearthcobaltalloyfilmsaresubstantiallyproducedbysputteringorvacuumplating.Ifsuchfilmsarepreparedbyelectrodepositioninstead,productionefficiencywouldbeimprovedandthecompositionofthealloycouldbecontrolled.Becausetheoxidationreductionpotentialsofrareearthelementsareverynegative,organicsolventsmaybeusedaselectrolyticmedia.ElectrodepositionofGdCoandSmCoinorganicsolutionshasbeenreporte...
简介:LayeredcathodematerialLiCo1/3Ni1/3Mn1/3O2wassynthesizedbyPechiniprocess,andinvestigatedusingX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andgalvanostaticcharge/dischargecycling.Thesampleiswell-crystallizedandhasaphase-purea-NaFeO2structure.Theparticlesizesareuniform,anddistributedintherangeof20-200nm.TheinitialdischargecapacityoftheLi/LiCo1/3Ni1/3Mn1/3O2cellwasabout149mAh·g-1whenitwascycledatavoltagerangeof4.5-2.3Vwithaspecificcurrentof0.25mA.Theresultisbetterincomparisonwithsolid-statesolutionmethod.Thesyntheticprocedurewasdiscussed.Threemajorreactions:chelation,esterification,andpolymerizationsuccessivelyoccurred.
简介:LaCrO_3的nano粉末被一条大音阶的第五音胶化线路准备。从350~550K的LaCrO_3nano粉末的热能力被DSC方法测量并且是表示了:C_(p(LaCrO3))(±0.112)=166.844-8.500x10~(-3)T-1.022x10~6T~(-2)(J/(摩尔·K))(350-550K)。一个EMF测量集会为流电的房间作为电解质与CaF_2被开发。可逆房间的FrommeasuredEMF数据,(-)磅,La_2O_3,LaF_3,|CaF_2|O_2(1atm),LaF_3,LaCrO_3,Cr_2O_3,磅(+),和吉布斯的相关价值释放的O_2(1atm)精力,吉布斯LaCrO_3的形成的免费精力从700~885K被计算:ΔG_(f,LaCrO3)~Θ=-1555.364+0.354T(kJ/mol)(700-885K)。并且免费精力从简单氧化物La_2O_3andCr_2O_3反应改变的吉布斯是打算的是:ΔG_(f,公牛(LaCrO3))~Θ=-94.758+8.530x10~(-2)T(kJ/mol)(700-885K)。
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:[1]S.Jin,T.H.Tiefel,M.McCormack,etal.:Sci-ence,264(1994),p.413.[2]R.vonHelmolt,J.Wecker,B.Holzapfel,etal.:Phys.Rev.Lett.,71(1993),p.2331.[3]Y.Shimakawa,Y.Kubo,T.Manako:Nature,379(1996),p.53.[4]C.Zener:Phys.Rev.,82(1951),p.403.[5]A.J.Millis,P.B.Littlewood,B.I.Shraiman:Phys.Rev.Lett.,74(1995),p.5144.[6]A.J.Millis,B.I.Shraiman,R.Mueller:Phys.Rev.Lett.,77(1996),p.175.[7]D.Louca,T.Egami,E.L.Brosha,:Phys.Rev.B,56(1997),p.8475.[8]G.Zhao,K.Conder,H.Keller,etal.:Nuture,381(1996),p.676.[9]C.H.Booth,F.Bridges,G.J.Snyder,etal:Phys.Rev.B,54(1996),p.15606.[10]K.H.Kim,J.Y.Gu,H.S.Choi,etal.:Phys.Rev.Lett.,77(1996),p.1877.[11]S.Zhou,G.Zhou,Y.Zhang:Jpn.J.Appl.Phys.,38(1999),p.5075.[12]S.Tajima,A.Masaki,S.Uchida,etal.:J.Phy.C:SolidStatePhys.,20(1987),p.3469.[13]L.M.Rodriguez-Martinez,J.P.Attfield:Phys.Rev.B,58(1998),p.2426.
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?????????????????@