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.
简介:Inthepasttenyearstheeomplementarytristimulusspeetrophotometryll],eTs,hasseenitsdiverseappli-eations{2一61thoughmostresearehesremaininrelativelysimpesystems,andlessworkhasbeeninvolvinkinetiereaetions.AnattemPthasbeenmadeontheinvestigationofsomecomPlieatedsystemseontainingrareearthsandmeta一acetylchloroPhosPhonaz
简介:
简介:Whitebody-color(Y,Gd)BxV1-xO4-x:Eu3+phosphorswerepreparedbycoprecipitationreaction.UnderVUVexcitationat147nm,theredemissioncolorimetricpurityof(Y,Gd)BxV1-xO4-x:Eu3+phosphorismuchbetterthanthatofcommercialPDP(plasmadisplaypanels)phosphor(Y,Gd)BO3:Eu3+.Butitsrelativeemissionintensityisonlyabout90%ofthecommercialphosphor.
简介:采用粉末冶金方法制备含Y2O3的稀土钼合金,利用金相显微镜、扫描电子显微镜(SEM)、X射线衍射(XRD)、能谱分析(EDS)等手段对钼合金的断裂特征和组织结构进行对比分析,研究稀土氧化物Y2O3含量对钼合金组织和性能的影响。研究表明:添加Y2O3能细化晶粒、改善钼合金的晶粒均匀性和致密度、提高钼合金的性能;拉伸强度和屈服强度随Y2O3含量的增加呈现先增高后降低的趋势,在Y2O3含量为1%时,抗拉强度达511.43MPa,屈服强度456.99MPa,分别是纯钼材料的1.31倍和1.57倍,综合力学性能最佳;在烧结坯中,Y2O3颗粒分布均匀,主要以球形和等轴状形式存在于晶界上。
简介:StudyonMorphologyofSurfaceofLargeAreaYBCOThinFilmsonZr(Y)O2SubstrateWangRuikun(王瑞坤),SunLihong(孙丽虹),LiuHongfei(刘鸿飞)WangXiaopi?..
简介:Thenanosizedparticlematerialsofdoped-TiO2withY2O3werepreparedbymeansofsol-geltechniqueforuseinelectrorheological(ER)fluids,andtheircrystalstructuresweremeasuredbyX-raydiffraction(XRD)analysis.TocomparewiththepureTiO2,adistinctenhancementintheshearstressunderdcelectricfieldwasfoundbyusingsuchmaterials.Thiscanbeexplainedbytheincreaseofthedielectriclossanddielectricconstantatlowfrequency.TheeffectsofthecrystalstructureoftheparticlesonthedielectricpropertyandERperformanceofmaterialswereinvestigated.
简介:Redphosphor(Y,Gd)BO3:Eu3+withgrainshape,smallsize,non-agglomerate,highcrystallinityandgoodphotoluminescence(PL)intensitywaspreparedbyacomplexmethodthattheprecursorofthephosphorwaspreparedbyco-precipitationmethodandthephosphorwaspreparedbycombustionmethod.TheSEMphotosandthephotoluminescencespectrumexcitedunderVUVshowthatthemorphologyandluminescentpropertiesofthisphosphoraresatisfiedwhenanappropriateamountofureawasadoptedasthecombustionagentinthepreparationprocedure.
简介:TheelectrodeprocessofY3+iononmolybdenumandnickelelectrodeshasbeenstudiedbycyclicvoltammetryandchronopotentiometryintheYCl3-NaCl-KClmelt.Theoverallchargetransferprocessisatwo-stepreaction:Y3++e=Y2+;Y2++2e=Y.YttriumreducedonthenickelelectrodecanformaseriesofNi-Yalloys.X-raydiffractionanalysiswasemployedtodeterminethealloycompositionsformedunderdifferentcon-ditions.
简介:以钴粉、氧化钇和草酸铵为原料,采用均匀沉淀法制备Co-Y2O3的前驱体,经氢还原后得到Co-Y2O3复合粉末,研究反应溶液中CoCl2浓度、YCl3与CoCl2的物质的量比n(YCl3)/n(CoCl2)以及表面活性剂对Co-Y2O3复合粉末形貌和粒度的影响。结果表明:YCl3与CoCl2的物质的量比以及表面活性剂对Co-Y2O3复合粉的形貌都有很大影响。当n(YCl3)/n(CoCl2)的值由0增加到0.014时,复合粉形貌由棒状转变为梅花状;当n(YCl3)/n(CoCl2)进一步增大到0.040和0.078时,复合粉分别为絮状和粗棒状;向n(YCl3)/n(CoCl2)为0.014的混合溶液中加入十二烷基硫酸钠时,复合粉末形貌由梅花形转变为球形。CoCl2的浓度c(CoCl2)对复合粉末粒度和分散性有较大影响。随c(CoCl2)从0.2mol/L增加到0.5mol/L,复合粉末的平均粒度由7μm减小到4μm,并且粉末的分散性更好;当c(CoCl2)增加到0.8mol/L时,粉末的平均粒度增大到10μm,粉末的分散性变差。
简介:VariousaffectingfactorsanddegradationmechanismwerestudiedonultrasonicdegradationofmethylorangeadoptingY2O3dopinganataseTiO2catalystpreparedinlaboratory.Intheexperiment,theUV-VISspectrophotometerwasusedtofollowandinspectthedegradationprocessofmethylorange.TheresultsindicatethattheultrasonicdegradationratiosofmethylorangeinthepresenceofanataseTiO2catalystaremuchbetterthanthosewithoutcatalyst.Moreover,thecatalyticperformanceofY2O3dopinganataseTiO2catalystisobviouslyhigherthanthatofanataseTiO2catalystwithoutdoping.TheoptimalconditionswereadoptedinthisworkandthedegradationandCODeliminationratioofmethylorangegotto98%and99.0%in90min,respectively.
简介:EffectofCe-Mg-Si(lightRE)andY-Mg-Si(heavyRE)nodulizersonthemicrostructuresandmechanicalpropertiesofheavysectionductileironwasinvestigatedtodevelopthematerialofspent-nuclear-fuelcontainers.Twoas-castsweretreatedbythesamequalitypercentageoflightREandheavyRE,respectively.Fourpositionswerechosentostandfordifferentsolidificationcoolingratesofspecimens.Thetensilestrength,elongationandimpacttoughnessofspecimenstreatedbyheavyREwereallhigherthanthoseofthespecimenstreatedbylightRE.Withthedecreaseofcoolingrate,themechanicalpropertiesoftwospecimensdecreased,andthefracturemorphologychangedfromductilefracturetobrittlefracture.TheimprovingeffectofmechanicalpropertiesbetweenheavyREandlightREwasobviousduetothebetteranti-degradationpropertyofheavyRE.Whilethesolidificationprocesslastedformorethan250min,theimprovingeffectwasnotobviousduetoseriousspheroidalizationdecaying.
简介:TheZrO2-Al2O3ceramiccompositeswerepreparedbyappropriatetechniqueswithcommercialZrO2andAl2O3powdersasrawmaterialsandY2O3asstabilizer.TheresultsindicatethatwiththeintroductionofAl2O3intotheZrO2matrixwherethequantityofadditiveY2O3is3.5%(molefraction),thegrowthofZrO2grainsisefficientlyinhibited,whichhelpstheZrO2grainsexistinametastabletetragonalmanner;thushigherstrengthandtoughnessareacquired.Whenthecontentofaluminais20%(massfraction),thebendingstrengthandfracturetoughnessofthecompositesare676.7MPaand10MPa·m1/2respectively,themechanicalbehaviorsareclosetothosepreparedwithZrO2andAl2O3powderssynthesizedthroughwetchemicalapproach.Themechanicalbehaviorsofthecompositesarewellimprovedowingtothedispersiontougheningofaluminagrainsandphasetransformationtougheningofzirconiagrains.
简介:采用光学显微镜(OM)、扫描电镜(SEM)、透射电镜(TEM)、显微硬度测试、热分析、能谱分析以及X射线衍射(XRD)等手段,研究Mg-10Gd-4.8Y-0.6Zr合金铸态和520℃固溶处理不同时间后的显微组织以及显微硬度分布。结果表明:Mg-10Gd-4.8Y-0.6Zr合金经520℃/16h固溶处理后,铸态时的网状共晶完全溶解到基体中,Gd、Y富集的立方体相弥散分布在晶内;晶内偏析消除,硬度有所降低。合金在固溶处理过程中发生以下组织演变:α-Mg固溶体+网状Mg24(GdY)5相→α-Mg固溶体+断续破碎的Mg24(GdY)5相→α-Mg过饱和固溶体+立方体相。该合金在520℃固溶处理的适宜时间为16h。
简介:文章研究了对Mg-9Gd-4Y-0.6Zr合金在时效过程中的微观组织。在225℃时效初期硬度缓慢上升,之后硬度急剧上升,24h出现了明显的时效硬化峰,然后硬度开始下降。微观结构的分析结果表明,在初期(2h)产生了大量弥散分布的具有DO19结构的β″,而在峰值时(24h)出现具有bco的β′,在持续时效(384h)时出现亚稳相β1,而在后来的长时间时效(1000h)时出现既在原位转变的平衡相β。