简介:LongafterglowphotoluminescentmaterialsSr2MgSi2O7dopedwithEu2+,Dy3+werepreparedbysol-gelmethod.ThesynthesizedsampleswerecharacterizedbyX-raydiffraction.Theexcitationspectrum,emissionspectrumandlongdecaycurveweremeasuredandanalyzed.XRDpatternindicatesthatphosphoriswithSr2MgSi2O7crystalstructure.Thewiderangeofexcitationwavelengthindicatesthatluminescentmaterialcanbeexcitedbylightfromultravioletraytovisiblelight.Themainpeakofemissionspectrumislocatedat466nm.Sampleexcitedbyvisiblelightcanemitbrightbluelight,andtheafterglowtimelastsmorethan8h.
简介:TheNaYF4:Yb,Ernanocrystalsweresynthesizedviathethermaldecompositionofmetaloleateprecursors.Thenanocrystalsinhexagonalstructurewerehighlyuniformandinsizeof25nm.Thebrightupconversionluminescencewasobservedundertheexcitationof980nmlaserandtheupconversionemissionspectrawereinvestigatedatdifferentpumppowers.Theemissionintensityratioofredlighttogreenlightlinearlyincreasedwithpumppowerincreasing.ThisresultindicatedthatthereexistedalargethresholdpowerofsaturationpumpforthefirstexcitationstateinNaYF4:Yb,Ernanocrystalscomparingtothatinbulkmaterial.
简介:Resinsofcomplexesmadefromagarose-Ce4+(RCA-Ce)andchitosan-Ce4+(RCC-Ce)wereprepared.Hydrolysisratesofmethamidophos,omethoateandchlorpyrifostreatedbyRCA-Cewere32.39%,27.12%and46.62%,respectively,thoseofchlorpyrifosandmethamidophosinmungbeansproutjuice38.28%and35.45%,andthatofchlorpyrifosinteaextract59.76%.HydrolysisratesofproteininteaextracttreatedbyRCA-Ceincreasedby86.46%.RCC-Cecouldbeemployedintheapplejuiceproduction.Thecontentsofmethamidophosandparathion-methylinthejuicetreatedbyRCC-Cedecreased58.76%and71.92%.Furthermore,RCC-Cewasusedtoclarificationforbeerbythewaysofacolumn.RCC-Cecouldhydrolyzesensitiveproteinandincreasecontentsoffreeaminoacidinthebeer.Therefore,thebeertreatedbyRCC-CecouldstayoxidationandagingprocedureduetosomemetalionsbeingabsorbedbyRCC-Ce.
简介:YbAl3(BO3)4crystalofgoodopticalqualitywasgrownbythefluxmethod.ThestructureofYbAl3(BO3)4crystalwasdeterminedbysingle-crystalX-raydiffraction.TheexperimentshowsthatYbAl3(BO3)4belongstothedoubleborateswithatrigonalstructure.ThespacegroupisR32anditsunitcellconstantsweremeasuredtobea=0.92965nm,c=0.72129nm,V=0.53673nm3,Z=3.Thetransmittancespectraweremeasured.Thecut-offofYbAl3(BO3)4crystalis216nm,andtherearetwoabsorptionpeakslocatedat940and975nmfrom190nmto2600nm.ThethermalpropertiesofYbAl3(BO3)4crystalwerestudiedforthefirsttime.Theaveragethermalexpansioncoefficientsweredeterminedtobe2×10-6/℃,9.5×10-6/℃alonga-andc-direction.ThespecificheatofYbAl3(BO3)4crystalwasmeasuredtobe0.6695J·(g·℃)-1atroomtemperature.AllresultsindicatethattheYbAl3(BO3)4crystalisanexcellentstoichioimetriclasermaterial.
简介:Thesynthesisofprecursorofgreenphosphors,LaPO4:Ce,Tb,bymeansofco-precipitationwithcocurrentflowfeedwasstudied.Theeffectsofthereactiontemperature,thekindandconcentrationoftheacidinthebottomwater,andthechargingrateonthephysicalproperties,suchasparticlesize,wereinvestigated.Itisfoundthattheparticlesizeofthepowderiscontrollablebyadjustingacidityinbottomwaterandchargingrate.Thepowderwithdiametersizeof3to5μmwasobtained.ItsXRDandSEMwereanalyzed.XRDpatternsoftheas-preparedgreenphosphorpowdersdisplaythetypicalpeaksofCePO4.SEMshowsthatthemorphologyofpowdersisball-shaped.
简介:Thenanosizedparticlematerialsofdoped-TiO2withY2O3werepreparedbymeansofsol-geltechniqueforuseinelectrorheological(ER)fluids,andtheircrystalstructuresweremeasuredbyX-raydiffraction(XRD)analysis.TocomparewiththepureTiO2,adistinctenhancementintheshearstressunderdcelectricfieldwasfoundbyusingsuchmaterials.Thiscanbeexplainedbytheincreaseofthedielectriclossanddielectricconstantatlowfrequency.TheeffectsofthecrystalstructureoftheparticlesonthedielectricpropertyandERperformanceofmaterialswereinvestigated.
简介:ToimprovethemechanicalpropertiesofWC-Al2O3composites,theeffectsoftraceamountofCeO2additivesonthemicrostructureandmechanicalpropertiesoftheWC-Al2O3compositespreparedbyhotpressingwereinvestigated.TheresultsrevealedthattheWC-Al2O3compositesdopedwith0.1%CeO2possessedrefinedmicrostructureandenhancedmechanicalpropertiescomparedwiththatoftheundopedWC-Al2O3composites.TraceCeO2suppressedthedecarburizationofWC,promotedthemicrostructuralrefinement,andimprovedtheinterfacecoherenceoftheWCmatrixandAl2O3.When0.1%CeO2wasaddedtotheWC-Al2O3composites,theeffectofCeO2resultedintheachievementofarelativedensityof98.82%withanexcellentVickershardnessof16.89GPa,combiningafracturetoughnessof9.85MPa·m1/2withanacceptableflexuralstrengthof1024.05MPa.
简介:Praseodymium(Pr)wasimpregnatedtoCeO2-ZrO2solidsolutionbyanimpregnationmethod.Theas-obtainedPrmodifiedCeO2-ZrO2wasimpregnatedwith1wt.%Pdtopreparethecatalysts.ThestructureandreducibilityofthefreshandhydrothermallyagedcatalystswerecharacterizedbyX-raydiffraction(XRD),Raman,X-rayphotoelectronspectroscopy(XPS),COchemisorptionandH2temperature-programmedreduction(H2-TPR).Theoxygenstoragecapacity(OSC)wasevaluatedwithCOservingasprobegas.EffectsofimpregnatedPronthestructureandoxygenstoragecapacityofcatalystswereinvestigated.TheresultsshowedthattheagedPr-impregnatedsampleshadmuchhigherOSCandbetterreducibilitythantheunmodifiedones.TheschemeofstructuralevolutionsofthecatalystswithandwithoutPrwasalsoestablished.PartialoftheimpregnatedPrdiffusedintothebulkofCeO2-ZrO2duringageing,whichinhibitedthesintering,andincreasedtheamountofoxygenvacanciesinCeO2-ZrO2support.Furthermore,thoseimpregnatedPrspecieswhichcoveredonthesurfaceofthesupportobstructedthestrongmetal-supportinteractionbetweenPdandCesoastoreducetheencapsulationofPdaswellasthebackspill-overoftheoxygenduringthecatalyticprocess.