简介:NanosizedBaCeo.95Yo.o5O3-δpowderswiththehomogeneouscompositionweresynthesizedbyanewcombustionprocessbasedonthePechinimethod.Apolymericprecursorsolwasformedbyuseofcitricacidandethyleneglycolasthechelatingagentsofmetalions.Theperovskite-typeBaCeo.95Yo.o5O3-δpowderswithuniformshapeandsmallerthan40nminsizedwereobtainedthroughthecombustionofthepolymericprecursorsolattheexistenceofnitricacidandammoniumhydroxide.Itwasfoundtheparticlesizecouldbecontrolledbymodulatingthequantitiesofnitricacidandammoniumhydroxide,thequantitiesoftheresidue,carbonateionswerealsoaffectedbythequantitiesofthecitricacidandethyleneglycol.
简介:采用金相组织观察、力学性能测试和统计分析等手段,研究了成品退火工艺对Φ5mmTP2内螺纹铜管微观组织和力学性能影响规律。结果表明:Φ5mmTP2内螺纹铜管退火温度为470~480℃时,铜管组织细小、均匀,同时能获得较高塑性和较高强度;490~500℃时,铜管晶粒尺寸、力学性能波动大;510~520℃时,铜管组织易粗大。Φ5mmTP2内螺纹铜管在470℃退火时,晶粒尺寸随退火时间的规律变化为d=0.0008t3-0.062t^2+1.7t-1.3,保温21min时,铜管再结晶基本完成,保温时间为28~31min时,铜管组织状态和综合力学性能最佳。
简介:ThesinglecrystalgrowthofstoichiometrichostluminescentcrystalNa5Eu(WO4)4hasbeeninvestigated.UsingNa2WO4asaflux,theoptimumconditionstogrowapuresinglecrystalbyflux-slow-coolingmethodhavebeendetermined.Ahighopticalqualitysinglecrystalofdimention4.5mmhasbeengrown,whichisthelargestoneasweknowsofar.Themicro-hardnessofNa5Eu(WO4)4singlecrystalis3.46×103MPa.Itsrefractiveindexis1.81inwhitelightwavelengthregionandthespecificgravityis5.65g/cm3.Thefluorescentandexcitationspectrahavebeendeterminedandthereasonofthefluorescentquenchof5D2and5D1to7FjofEu3+canbeexplainedasmulti-phononnon-radiationtransition.
简介:Thesimplemodelfor4f-5dtransitionsoflanthanideionsincrystalswasextendedtodealwiththecaseoftheoctahedralcrystalfield,whereforthet2componentof5dorbitalsthespin-orbitinteractioncouldnotbeneglectedduetoincompletequenchingofthe5dorbitalangularmomentum.Theenergylevelsforthe4fN-15dconfigurationandtherelativelinestrengthsforthe4fN4fN-15dtransitionwerecalculatedindetail.Theresultwasappliedtotheinterpretationofthelow-temperature4f-5dexcitationspectrumofCs2NaYCl6∶Tb3+.
简介:YPO_4phosphorssingle-dopedwithSb~(3+)orGd~(3+)andco-dopedwithSb~(3+)andGd~(3+)werepreparedbyasolid-statereactionmethod.Thephasepurity,morphology,photoluminescenceexcitationandemissionpropertiesofthepreparedphosphorswereinvestigated.TheresultsshowedthatSb~(3+)couldsensitizeGd~(3+)intheco-dopedphosphorswhichmadethephosphorsexcitablebyshort-waveultraviolet(UV)atawavelengthbetween220and260nm.Under253.7nmexcitation,theco-dopedphosphorsY_(1–x–y)PO_4:Sb~(3+)x,Gd~(3+)yshowedstrongemissionofGd~(3+)atawavelengthof312nmwhoseintensitychangedwiththedopingconcentrationsofGd~(3+)andSb~(3+).TheoptimizedY_(0.77)PO_4:Sb~(3+)0.07,Gd~(3+)0.16phosphorshowedanintensitycomparabletocommercialLaPO_4:Cephosphor(UVB-315),makingitapotentialcandidateformercurylow-pressuredischargenarrow-bandUV-Bemittinglamps.
简介:LuminescencelifetimeofCe(Ⅲ)forCe0.9RE0.1P5O14,whereREdenotesrareearthionsotherthanCe(Ⅲ),wasmeasuredbymeansofthetime-correlatedsinglephotoncountingtechnique.Ithasbeenfoundthatthelifetimedataarecapableofelucidatingtheenhancementorquenchingofcerium(Ⅲ)luminescencebyalienREions(otherthanCe)indoublydopedceriumpentaphosphatecrystal.
简介:Theeffectofanexternalelectricfieldonthecrystallizationbehaviorofamorphous(Nd0.1Fe0.9)3Balloywasinvestigated.ThecrystallizationproductofNd2Fe23B3phasewasobtainedforthisamorphousalloyannealedat923Kfor300sinthepresenceofanexternalelectricfieldof300kV·m-1(50Hz);whilethecrystallizationproductsareNd1.1Fe4B4,α-Fe,andFe3Bphasesunderthesameannealingconditionexceptforfree-electricfield.Ontheotherhand,thesampleswereannealedat1023K,whichishigherthanthedecompositiontemperatureofmetastableNd2Fe23B3phase,for600s.Inthecaseofthepresenceofanexternalelectricfield,themetastableNd2Fe23B3phase,asamainphase,isstillstayedinthesample.ThisfactsuggeststhattheexternalelectricfieldenhancesthestabilizationofthemetastableNd2Fe23B3phase.Theeffectoftheexternalelectricfieldonthephaseselectionandstabilizationwasexplainedintermsofthespecificconductancedifferencebetweenthecrystallizationproducts.
简介:Loadedonthecordierite,therareearthdopedcompositecatalystwaspreparedbysol-gelmethodcombinedwithdippingtechnique.TakingOrthodichlorobenzeneasmodel,thecatalystwasusedtoremovethedioxinsofthewastegas.Theresultsshowedthatat280℃andgasspacevelocitybeing8000h-1,theorthodichlorobenzenecouldberemovedeffectivilybythepreparedCeO2-TiO2-V2O5compositecatalystwhoseactivitywasremarkablyenhancedbythedopingofCe,whiletheindustrialside-streamtestofdioxinsfromrefuseincinerationsmokeindicatedthatthedecompositionratecouldreachabove93%underthesameconditions.
简介:TheNd60Fe20Al8Co10B2alloywaspreparedbysuctioncastingofthemoltenalloyintoacoppermoldunderargonatmosphere.Themicro-structuralandmagneticpropertychangesintheNd60Fe20Al8Co10B2alloyduringcrystallizationwereinvestigatedbyX-raydiffraction(XRD),differentialscanningcalorimetry(DSC),scanningelectronmicroscope(SEM)andthevibratingsamplemagnetometer(VSM).TheprecipitationandNd-richandFe-richphaseshavenosignificanteffectontheintrinsiccoercitityforNd60Fe20Al8Co10B2alloyannealedbelow723K.However,thegrowthofFe-richphasedecreasesthesaturatemagnetizationandremanenceofthealloy.Thehardmagneticbehaviorisdisappearedwhenthealloyisfullycrystallized.
简介:La15Fe77B8hydrogenstoragealloyswerepreparedusingavacuuminduction-quenchingfurnace.TheresultsofX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM)suggestedthatLa15–xSmxFe2Ni76Mn5B2(x=0,2,4,6)alloyshadmultiphasestructureincludingthemainLaNi5phase,La3Ni13B2phaseand(Fe,Ni)phase.WiththeincreasingsubstitutionofSmforLa,themainphasestructureofalloysdidnotchange,whiletheunitcellvolumesdecreased,thecyclestabilitywasimprovedandthemaximumdischargecapacitydecreased,butthelowtemperaturemaximumdischargecapacityofthesamesubstitutionalloywasgraduallyapproachingthemaximumdischargecapacityatroomtemperature,whichshowedthatLa15Fe77B8hydrogenstoragealloysofthepartialsubstitutionofSmforLahadbetterlow-temperaturedischargeability(LTD).Forthesamesubstitutionalloys,self-dischargecharacteristicsandcyclestabilityatlowtemperaturewerebetterthanthatatroomtemperature.Furthermore,thehigh-ratedischargeability(HRD)andtheexchangecurrentdensityI0firstincreasedandthendecreasedwiththeincreasingofSmcontent,whereasthehydrogendiffusioncoefficientDinalloybulkdecreasedgradually,whichindicatedthatappropriatesubstitutionofSmforLaimprovedtheelectrochemicalkineticspropertiesofthealloys.TheHRDwasmainlydominatedbythecharge-transferrateonthealloysurface.
简介:TheeffectofrapidsolidificationonstructureandelectrochemicalperformanceoftheLaNi4.5Co0.25Al0.25hydrogenstoragealloywasinvestigatedbyX-raypowderdiffractionandasimulatedbatterytest,includingmaximumcapacity,cyclingstability,self-discharge,andhigh-ratedischargeability(HRD).Allthemelt-spunalloysweresingle-phasewiththeCaCu5-typestructure(spacegroupP6/mmm).Incomparisontotheas-castalloy,therapidlyquenchedalloysmanifestedanimprovedhomogeneityofcompositionandexpandedlatticeparameters.Theelectrochemicalmeasurementsshowedthattheactivationproperty,cyclingstabilityandself-dischargeofthealloyelectrodeswerealsoimprovedfortherapidsolidifiedalloys.TheHRDoftheas-castalloywasbetterthanthoseofalltherapidlysolidifiedalloys.Asthequenchingrateincreased,theHRDandexchangecurrentdensityfirstdecreasedandthenincreased.
简介:Thephasesandmagnetocaloriceffectinthealloys(Gd1-xErx)5Si1.8Ge2.2withx=0,0.1,0.2and0.3wereinvestigatedbyX-raydiffractionanalysisandmagnetizationmeasurement.ThesamplesweresinglephasewiththemonoclinicGd5Si2Ge2-typestructure.WiththeincreaseofErcontent,theCurietemperature(Tc)decreasedobviouslyfrom253Kofthealloywithx=0to114Kwithx=0.3.Themaximummagneticentropychangedinthesamplesof(Gd1-xErx)5Si1.8Ge2.2withx=0.0,0.1,0.2and0.3were6.88,8.32,9.59and10.24J·kg-1·K-1respectivelyintheappliedfieldchangeof0~2.0T.