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简介：ThephaseandmorphologytransformationduringthehydrothermaltreatingprocessofY2O3wasevaluatedwithX-raydiffcrcnce(XRD),scanningelectronmicroscopy(SEM),transmissionelectronmicroscopy(TEM),particlesizeandspecificsurfaceareadetermination.TheresultsshowedthatthecubicY2O3didnottransferintohexagonalY(OH)3inpurewater.Therefore,purehexagonalY(OH)3withnanotubeandmicrorodmorphologieswereobtainedbyhydrothermaltreatingY2O3at150℃for12hin15mlof2mol/LNaOHsolutionwithandwith-outPVAorPEGItwassuggestedthatthecharacteristicpreferentialgrowthofY(OH)3wasattributedtothestructureanisotropyofhexahedronY(OH)3.TheadditionofPVAorPEGcouldpromotetheformingprocessofnanotubesbyselectiveadsorptionondifferentcrystalplanes,whichalteredthegrowthratealongdifferentdirectionsandresultedinthediffusionlimitofconstructingionsinthecentertopofrods.Finally,Y(OH)3:EuandY2O3:Eunanotubeswerealsosynthesizedbyusingthismethod,andtheirphotoluminescencepropertieswereevaluated.

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简介：Thesinglecrystalofthecomplex[Sc（NO3）3（H2O）2]·（15C5）hasbeenpreparedinacetonitrile.Thenewcomplexhasbeencharacterizedbyelementalanalysis,IRspectra,solubilityandmolarconductancemeasurements.ThestructureofthecomplexisdeterminedbysinglecrystalX-raydiffractionanalysis.

简介：ＥｌｅｃｔｒｏｎＭｉｃｒｏｓｃｏｐｉｃＩｎ－ｓｉｔｕＯｂｓｅｒｖａｔｉｏｎｆｏｒＰｒｅｐａｒａｔｉｏｎｏｆＵｌｔｒａｆｉｎｅＬａ２Ｏ３ＮａｎｏｐｈａｓｅＰｏｗｄｅｒＧａｏＹｕｚｕｎ（高愈尊），ＬｉＹｏｎｇｈｏｎｇ（李永洪），ＺｈａｎｇＴａｉｓｏｎｇ...

简介：做Gd或做Lu的长晚霞红黄磷Y2O2S:Sm(3+)用高温度流动熔化方法被综合。获得的黄磷用X光检查衍射被分析决定晶体结构，并且阶段分析产品在单个阶段的表演。光系列和腐烂曲线在一个日立F-4500荧光分光光度计上被测量。腐烂时间在一个ST-900PM弱轻光度计上被决定。分析证明陆做的那位主人改进材料的光和腐烂时间。做的陆和Sm的集中被改变以便决定最佳的条件并且综合有最好的性质的产品。长晚霞的机制简短也被讨论。

简介：Organicsubstancesuchassolventandresin'seffectonluminescentcapabilityofSrAl2O4:Eu2+,Dy3+phosphorwasstudied.Someorganicsolventsandresinswereselectedforexperimentation.TheresultsindicatethatthoseorganicsolventswillnothavenegativeeffectontheappliedcapabilityofSrAl2O4:Eu2+,Dy3+phosphor.Adoptingtheorganicresinsandcoveringmethod,theafterglowluminanceofSrAl2O4:Eu2+,Dy3+phosphorwasincreasedby85.01%and82.51%.

简介：AseriesofCe0.5Fe0.30Zr0.20O2catalystswerepreparedbydifferentmethods(co-precipitationsmethod,citricacidsol-gelmethod,impregnationmethod,physicalmixedmethod,andhydrothermalmethod)andcharacterizedbyX-raydiffraction(XRD),Ramanspectroscopy,Brunauer-Emmett-Teller(BET)andH2-TPRmeasurements.Potentialofthecatalystsinthesootoxidationwasevaluatedinatemperature-programmedoxidation(TPO)apparatus.TheresultsshowedthatalltheFe3+andZr4+wereincorporatedintocerialatticetoformapureCe-Fe-Zr-Osolidsolutionfortheco-precipitationsample,buttwokindsofFephasesexistedintheCe-Fe-Zr-Ocatalystspreparedbyothermethods:Fe3+incorporatedintoCeO2latticeanddispersedFe2O3clusters.ThefreeFe2O3clusterscouldimprovetheactivityofcatalystsforsootoxidationcomparingwiththepureCe-Fe-Zr-OsolidsolutionowingtothesynergeticeffectbetweenfreeFe2O3andsurfaceoxygenvacancies.Inaddition,theactivityofcatalystsstronglyreliedonthesurfacereducibilityoffreeFe2O3particles.HoldingbothabundantfreeFe2O3particlesandhighoxygenvacancyconcentration,thehydrothermalCe0.5Fe0.3Zr0.2O2catalystpresentedthelowestTi(251°C,ignitiontemperatureofsootoxidation)andTm(310°C,maximumoxidationratetemperature)forsootcombustion(withtight-contactbetweensootandcatalysts)amongthefivesamples.Evenafteragingat800°Cfor10h,theTiandTmwerestillrelativelylow,at273and361°C,respectively,indicatinghighcatalyticstability.

简介：高度有效的Tb3+激活SrAl2O4黄磷被一个联合combustionsolid状态反应方法综合。SrAl2O4的先锋:Tb3+黄磷经由一个燃烧过程被准备，然后同样准备的粉末被加热在一减少在1250点的激活的碳周围??慥獲？

简介：ThemorphologyandcorrosionbehaviorofNi/Al2O3compositecoatingspreparedusingdouble-pulsedelectrodepositingtechniqueafteroxidizedunder800℃NaCldepositinairenvironmentwereanalyzedbyscanningelectricalmicroscope(SEM),X-raydiffraction(XRD)andenergydispersivespectrum(EDS).TheresultsshowedthatthecorrosionofallcompositecoatingswasacceleratedunderNaCldeposits,andthecorrosionproductswereratherporouswithpooradherencetothematrix.Al2O3particlesinthecoatingscanrefinethegrainsizeandimprovethehightemperaturecorrosionresistanceofthecoatings.Withinthetestscope,themoreAl2O3particlesinthecoatings,thelowercorrosionratescouldbeobtained,andthecorrosionmechanismwasalsodiscussed.

简介：LongafterglowphotoluminescentmaterialsSr2MgSi2O7dopedwithEu2+,Dy3+werepreparedbysol-gelmethod.ThesynthesizedsampleswerecharacterizedbyX-raydiffraction.Theexcitationspectrum,emissionspectrumandlongdecaycurveweremeasuredandanalyzed.XRDpatternindicatesthatphosphoriswithSr2MgSi2O7crystalstructure.Thewiderangeofexcitationwavelengthindicatesthatluminescentmaterialcanbeexcitedbylightfromultravioletraytovisiblelight.Themainpeakofemissionspectrumislocatedat466nm.Sampleexcitedbyvisiblelightcanemitbrightbluelight,andtheafterglowtimelastsmorethan8h.

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简介：Er3+-Tm3+-Yb3+tri-dopedBaMoO4phosphorsweresynthesizedbyco-precipitationtechniqueandcharacterizedbyX-raydiffractionanalysis,absorptionstudyandfieldemissionscanningelectronmicroscopyanalysis.Upconversionaswellasdownconversionluminescencestudieswereperformedbyusingnearinfrared（980nm）andultraviolet（380nm）excitations.Energyleveldiagram,pumppowerdependenceandcolourcoordinatestudywereutilizedtodescribethemulticolorupconversionemissionproperties.Undersingle980nmdiodelaserexcitationthedualmodesensingbehaviourisrealizedviaStarksublevelsandthermallycoupledenergylevelsoftheTm3+andEr3+ionsinthepreparedtri-dopedphosphors.AcomparativefluorescenceintensityratioanalysisforintegratedemissionintensitiesarisingfromtheStarksublevels{1G4（a）and1G4（b）}andthermallycoupledenergylevels{2H11/2and4S3/2}oftheTm3+andEr3+ions,respectivelywascarriedoutinthepreparedtri-dopedBaMoO4phosphors.ThemaximumsensitivityforthermallycoupledenergylevelsoftheEr3+andStarksublevelsoftheTm3+ionwasreported.Thedevelopedphosphorscouldbeusefulinthedisplaydevicesandopticalthermometricapplications.

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简介：是的Gd2O3薄电影高--门电介质被磁控管在1.3Pa和不同温度的一个压力劈啪作响在Si(001)底层上直接扔。X光检查衍射结果揭示了那从450～570慮挠牥浡捩洠瑡牥慩獬?潈?牰獥楳杮眠獡甠敳?潴映'L楲慣整愠畬業慮洠瑡楲?潣灭獯瑩獥椠?楮牴杯湥愠浴獯桰牥?牰瑯'虡N湯?楍牣獯牴'壮肭?种的所有电影湡?敭档湡捩污瀠潲数瑲敩?景琠敨挠浯潰楳整?敷敲琠獥整???慷?湩楤慣整?桴瑡琠敨戠湥楤杮猠牴湥瑧?湡?牦捡畴敲琠畯桧敮獳漠?污浵湩?慭牴硩挠牥浡捩挠浯潰楳整?楳瑮牥摥愠?????P

简介：DirectextractionofmetalsfromsolidswithcomplexingagentsinsupercriticalCO2(SC-CO2)hasrecentlyattractedinterestsinseparation,purification,recovery,andanalysisofmetals.Inthepresentstudy,thestatic/dynamicextractionofrareearthelements(Nd,Ce)fromtheiroxides(Nd2O3,CeO2)withorganophosphoruscomplexeswithHNO3andH2OinSC-CO2wasinvestigated.ThestaticextractionefficiencyofNdfromNd2O3withthetri-n-butylphosphate(TBP)-HNO3complexcouldreach95%underoptimizedexperiment...

简介：NanosizedBaCeo.95Yo.o5O3-δpowderswiththehomogeneouscompositionweresynthesizedbyanewcombustionprocessbasedonthePechinimethod.Apolymericprecursorsolwasformedbyuseofcitricacidandethyleneglycolasthechelatingagentsofmetalions.Theperovskite-typeBaCeo.95Yo.o5O3-δpowderswithuniformshapeandsmallerthan40nminsizedwereobtainedthroughthecombustionofthepolymericprecursorsolattheexistenceofnitricacidandammoniumhydroxide.Itwasfoundtheparticlesizecouldbecontrolledbymodulatingthequantitiesofnitricacidandammoniumhydroxide,thequantitiesoftheresidue,carbonateionswerealsoaffectedbythequantitiesofthecitricacidandethyleneglycol.

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简介：Inthiswork,boththethermalexpansionandelectricalconductivityofnanocrystallineLa2Mo2O9werestudied.ThenanocrystallinepowderofLa2Mo2O9wasobtainedbysol-gelmethod,andwiththehelpofSHP(superhighpressure)upto4.5×104atmat700℃forashorttime,andthenanocrystallinepowderwasdensifiedwithoutobviousparticlesizegrowth.TheelectricalconductivityofnanocrystallineLa2Mo2O9wasoneorderofmagnitudelowerthanthatofthemicrocrystallinesampleatthesametemperature.Owingtothephasetransition,themicrocrystallineLa2Mo2O9hasanabruptincreaseofthermalexpansionwithapeakvalueof48×10-6K-1at556℃.Forthenanocrystallinematerial,thepeakvalueincreasesto112×10-6K-1at520℃.Ontheotherhand,above600℃thesignificantgrowthofparticlesizeofthenanocrystallineLa2Mo2O9wasobserved,accompanyingbyatremendousincreaseofthermalexpansionwithapeakvalueofthirdhigherthanthatofLa2Mo2O9.