简介:VariousaffectingfactorsanddegradationmechanismwerestudiedonultrasonicdegradationofmethylorangeadoptingY2O3dopinganataseTiO2catalystpreparedinlaboratory.Intheexperiment,theUV-VISspectrophotometerwasusedtofollowandinspectthedegradationprocessofmethylorange.TheresultsindicatethattheultrasonicdegradationratiosofmethylorangeinthepresenceofanataseTiO2catalystaremuchbetterthanthosewithoutcatalyst.Moreover,thecatalyticperformanceofY2O3dopinganataseTiO2catalystisobviouslyhigherthanthatofanataseTiO2catalystwithoutdoping.TheoptimalconditionswereadoptedinthisworkandthedegradationandCODeliminationratioofmethylorangegotto98%and99.0%in90min,respectively.
简介:Thenoveleomplexesofalkaliandrareearthmetalwithperiodatehavebeenpreparedforthefirsttime.ChemicalanalysisindicatesthatthecompositionofthecomplexesisM2LnIO6·xH2O(M=Li,Na,K;Ln=Pr,Tb),andallofthecomplexeshavebeencharacterizedbyUV-Visible,IRspectroscopicstudies,susceptibilitymeasurementsandthermalanalysis.
简介:EffectofMnsubstitutionforFeincubicLavesZr0.1Tb0.9(Fe1-xMnx)2andY0.1Tb0.9(Fe1-xMnx)2com-poundsispresented.Similarresultsinbothsystemsareobtained:ThestructureandthemagnetismofTbFe2arebothinfluencedslightlybyasmallamountofYorZrsubstitutionforTb;Withincreasingxvalue,thelatticeconstantincreasesmonotonously;theCurietemperaturedecreaseslinearly;whilesaturationmagnetizationincreaseslinearly.ForthesmallamountofMnsubstitutionforFeinbothsystems,magnetostrictionissignificantlylargerthanthatinthepureironalloys.Thelargestmagnetostrictionof|γ‖-|γ|=2200×10-6atmagneticfieldof2×107/4πA/misobtainedforY0.1Tb0.9(Fe0.95Mn0.052.
简介:Sm0.2Ce0.8O1.9(SDC)electrolytewaspreparedbyamodifiedsolidstatemethodatrelativelylowsinteringtemperatureswithoutanysinteringpromoters.ThephasecompositionandmicrostructureoftheelectrolyteswereinvestigatedbyX-raydiffraction(XRD)andfieldemissionscanningelectronmicroscopy(FESEM)technologies.ArelativedensityofSDCelectrolytesinteredat1300oCreached97.3%andthemeanSDCgrainsizewasabout770nm.Theirionicconductivityandthermalexpansioncoefficientwerealsomeasuredbyelectrochemicalworkstationanddilatometer.Theelectrolyteattainedahighconductivityof5×10–2S/cmat800oCwithanactivationenergyof1.03eVandaproperthermalexpansioncoefficientof12.6×10–6K–1.
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:在甲烷(POM)的部分氧化的催化活动和稳定性混合方法的CeO2-ZrO2和-Al2O3的影响在Ni/Ce0.7Zr0.3O2-Al2O3催化剂上被调查。催化剂被XRD,TPR,H2-chemsorption,和TG-DTA描绘。为新鲜催化剂,结果证明混合催化剂(原子)的盐先锋比混合方法(摩尔)和机械地混合方法(MECH)的粉末的催促的人准备的催化剂介绍了更好的性能。XRD的结果建议在在原子样品的CeO2-ZrO2和Al2O3之间的相互作用比其它强壮,它导致了更多的格子缺点和从而更好的起始的活动。而且,MECH样品在24h稳定性测试有最好的稳定性和最少的焦炭免职。TPR和H2-chemsorption的结果显示在MECH样品的Ni-Al的亲密接触提高了抵抗焦炭免职和金属sintering的能力。
简介:YLiF4:Er3+wassynthesizedbyhydrothermalmethod.ConcentrationofEr3+ischangedfrom0to5%.TheabsorptionofEr3+inallsamplesfrom200to1200nmwasmeasuredatroomtemperature.TheJ-OparameterscalculatedfromabsorptionspectrumareΩ2=1.05×10-20cm2,Ω4=1.25×10-20cm2andΩ6=1.35×10-20cm2.Infrared-to-visibleupconversionemissionofYLiF4:Er3+wasobservedwhenexcitedby980nm.TheresultsshowthattheEr3+contentislessthan1.5%,excite-stateabsorptionisthemainmechanismofupconversionemission.WhenEr3+contentislargerthan1.5%,bothoftheexcite-stateabsorptionandenergytransferleadtotheupconversionluminescence.TheupconversionintensitywasenhancedwiththeincreasingofEr3+concentration.Atroomtemperature,thelifetimeof2H11/2and4S3/2is205μswhilethatof4F9/2is188μsforsampleEr-2.Thetransitionratesandquantumefficiencywerealsocalculated.Thequantumefficienciesof4S3/2and4F9/2are27.9%and10.7%,respectively.
简介:二进制铕建筑群EuL3(L=4-tert-butylbenzoate)和第三的铕建筑群EuL3TTA0.1(TTA=2-thenoyltrifluoroacetone),EuL3DBM0.5(DBM=dibenzoylmethane)和EuL3phen0.5(phen=1,10-phenanthroline)被综合。poly(甲基methacrylate)(PMMA)或有composites与铕建筑群做了的丙烯酸的酸(AA)的甲基methacrylate(MMA)的共聚物被基在原处准备聚合。铕建筑群,ligands,N,N-dimethylformamide(DMF)和做的聚合物的光性质上的单体的影响被调查。结果证明二进制、第三的建筑群的荧光刺激乐队根据他们的紫外吸收乐队。所有建筑群和做的聚合物composites展出了Eu3+离子的敏化ligand的红典型排放。聚合物composites的荧光紧张在EuL3/PMMA的顺序增加了