简介:TheZrO2-Al2O3ceramiccompositeswerepreparedbyappropriatetechniqueswithcommercialZrO2andAl2O3powdersasrawmaterialsandY2O3asstabilizer.TheresultsindicatethatwiththeintroductionofAl2O3intotheZrO2matrixwherethequantityofadditiveY2O3is3.5%(molefraction),thegrowthofZrO2grainsisefficientlyinhibited,whichhelpstheZrO2grainsexistinametastabletetragonalmanner;thushigherstrengthandtoughnessareacquired.Whenthecontentofaluminais20%(massfraction),thebendingstrengthandfracturetoughnessofthecompositesare676.7MPaand10MPa·m1/2respectively,themechanicalbehaviorsareclosetothosepreparedwithZrO2andAl2O3powderssynthesizedthroughwetchemicalapproach.Themechanicalbehaviorsofthecompositesarewellimprovedowingtothedispersiontougheningofaluminagrainsandphasetransformationtougheningofzirconiagrains.
简介:采用Nb2O3、Y2O3复合稳定剂,制得了高韧性、高强度的四方相ZrO2陶瓷材料,发现在Y2O3-ZrO2材料中加入0.5~1molNb2O3,可使材料在保持原有抗弯强度的同时,一定程度上改善了断裂韧性和相组成。
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:基于国外定向凝固氧化物/氧化物共晶复合陶瓷的晶体生长动力学行为的研究成果,阐述其动力学机制,分析动力学因素对微观结构形态的影响,探讨晶体生长热力学、动力学行为与微观结构形态之间的关系,同时结合以燃烧合成、快速凝固技术制备的新型高强韧A12O3/ZrO2(Y2O3)共晶复合陶瓷,探讨共晶复合陶瓷在快速凝固条件下的晶体生长动力学行为。结合定向凝固与快速凝固两种晶体生长机制,得知过冷度、凝固界面前沿的温度梯度是影响晶体生长方式的重要因素,且受二者决定的凝固速率(即晶体生长速率)则决定材料的最终微观结构与形态。
简介:VariousaffectingfactorsanddegradationmechanismwerestudiedonultrasonicdegradationofmethylorangeadoptingY2O3dopinganataseTiO2catalystpreparedinlaboratory.Intheexperiment,theUV-VISspectrophotometerwasusedtofollowandinspectthedegradationprocessofmethylorange.TheresultsindicatethattheultrasonicdegradationratiosofmethylorangeinthepresenceofanataseTiO2catalystaremuchbetterthanthosewithoutcatalyst.Moreover,thecatalyticperformanceofY2O3dopinganataseTiO2catalystisobviouslyhigherthanthatofanataseTiO2catalystwithoutdoping.TheoptimalconditionswereadoptedinthisworkandthedegradationandCODeliminationratioofmethylorangegotto98%and99.0%in90min,respectively.
简介:Inthisstudy,factorsaffectingthecrystalstructureofflame-synthesizedY2O3:Euparticleswereinves-tigated,especiallytheparticlesizeeffectanditsinteractionwithEudopingconcentration.PolydisperseY2O3:Eu(sizerange200nmto3m)powdersampleswithEudopingconcentrationsfrom2.5mol%to25mol%weregeneratedineitherH2/airorH2/O2substrate-freeflames.ThecrystalstructureofthepowdersampleswasdeterminedbypowderX-raydiffraction(XRD),whichwascomplementedbypho-toluminescence(PL)measurements.Singleparticlecrystalstructurewasdeterminedbysingleparticleselectedareaelectrondiffraction(SAED),andforthefirsttime,byelectronbackscatterdiffraction(EBSD).H2/airflamesresultedincubicphaseY2O3:Euparticleswithhollowmorphologyandirregularshapes.ParticlesfromH2/O2flameshaddenseandsphericalmorphology;sampleswithlowerEudopingconcen-trationshadmixedcubic/monoclinicphases;sampleswiththehighestEudopingconcentrationswerephase-puremonoclinic.ForsamplesgeneratedfromH2/O2flames,aparticlesizeeffectanditsinteractionwithEudopingconcentrationwerefound:particlessmallerthanacriticaldiameterhadthemonoclinicphase,andthiscriticaldiameterincreasedwithincreasingEudopingconcentration.Thesefindingssug-gestthattheformationofmonoclinicY2O3:Euisinevitablewhenextremelyhotsubstrate-freeflamesareused,becausetypicalflame-synthesizedY2O3:Euparticlesizesarewellbelowthecriticaldiameter.However,itmaybepossibletogenerateparticleswithdense,sphericalmorphologyandthedesiredcubicstructurebyusingamoderatelyhighflametemperaturethatenablesfastsinteringwithoutmeltingtheparticles.
简介:摘要:金刚石工具作为一种新兴的超硬材料制品,是对传统工具的一种革命性替代和跨越性发展,广泛应用于各类硬脆非金属材料及部分金属材料的切、磨、钻、铣、抛等加工领域,涉及建筑、建材、石油、地质、冶金、机械、电子、陶瓷、木材、汽车等工业。近年来,随着大宗商品的价格上涨,金刚石工具成本上升幅度巨大,成本更加优势的铁基金刚石工具得到了迅猛的发展,但铁基胎体的工艺范围狭窄及合金化程度不足,导致产品性能不稳定,在一定程度上限制了其发展。Y2O3作为一种优良的增韧填料,能够改善铁基金刚石工具的力学性能和耐用度。本文以铁基胎体为主要原料,采用添加Y2O3的方法,研究了Y2O3含量对铁基金刚石工具的硬度、抗弯强度、断裂韧性和耐磨性的影响,以供参考。
简介:FourkindsofY2O3stabilizedZrO2(YSZ)thinfilmswithdifferentY2O3contents(from0to12mol%)aredepositedonBK7glasssubstratesbyelectron-beamevaporationmethod.TheeffectsofdifferentY2O3dopantcontentsonresidualstress,structure,andopticalpropertiesofZrO2thinfilmsareinvestigated.TheresultsshowthatresidualstressinYSZthinfilmsvariesfromtensiletocompressivewiththeincreaseofY2O3molarcontent.TheadditionofY2O3isbeneficialtothecrystallizationofYSZthinfilmandtransformationfromamorphoustohightemperaturephase,andtherefractiveindexdecreaseswiththeincreaseofY2O3molarcontent.Moreover,thevariationsofresidualstressandtheshiftsofrefractiveindexcorrespondtotheevolutionofstructuresinducedbytheadditionofY2O3.
简介:有不同Y_2O_3内容的基于钴的合金被扔用血浆的onQ235A碳钢转移了焊接机器的弧(PTA)。微观结构上的Y_2O_3的效果并且穿基于钴的合金的抵抗性质用一台光显微镜,一台扫描电子显微镜(SEM),X光检查衍射(XRD),和传播电子被调查显微镜学(TEM)。有face-centeredcubic晶体结构的一个基于钴的稳固的答案被介绍,这被发现在Y_2O_3免费的基于钴的合金涂层与六角形的晶体结构由第二等的阶段M_7C_3伴随了。几叠差错在基于钴的稳固的答案存在。Y_2O_3的增加在修改Y_2O_3的涂层导致Y_2O_3阶段的存在。尽管叠差错在修改Y_2O_3的涂层存在,它的密度增加。Y_2O_3的增加能精制微观结构并且当它的内容小于等于0.8wt.%时,能增加wear抵抗性质。然而,它的内容的另外的增加将在γ-Cograin边界导致undissolvedY_2O_3粒子的凝块,并且将导致粗糙的微观结构并且降低穿抵抗性质。
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简介:TheRamanspectraof3%(molefraction)Y2O3-ZrO2(3Y)areobtainedatdifferenttemperaturefrom77Kto853K.Theresultsshowthat260cm-1Egand460cm-1Egmodesonthespectrashifttowardlowerwavenumberwiththeincreaseoftemperature;meanwhile,thecontinuityoftheHalfWidthatHalfMaximum(HWHM)andwavenumber(frequency)ofRamanbandsarebrokenandt-phaseonlypartiallytransformstom-phaseat523K.Basedontheexperimentalresults,thispaperdiscussesthet-phaselatticevibrationof3YandpresentstheimagesofvibrationdisplacementofsixRaman-activemodesfort-phaseofZrO2.TheanalysisindicatesthattherearediversitiesexistinginthedisplacementoftheatomicvibrationofRaman-activemodesbecauseoftheirdifferentsymmetriesatvarioustemperature,whichleadstothedifferentchangetendenciesofRamanbands.Furthermore,theabruptchangesofsomeRaman-activemodesindicatingtheatomicdisplacementareassumedtobethecondensationsofphononmodesinthet→mphasetransition.
简介:NewrareearthvanadatesYSrQ-xCaxV3O9-y(x=0.0,0.67,1.0,1.33and2.0)havebeensynthesizedbyanewsimplemethod.X-raypowderdiffractionresultsshowthattheyaremono-phase.Theybelongtoorthorhombicstructureandtheirlatticeconstantsarecalculated.TheresultsofweightgainsinTGcurvesshowthatthelowervalentvanadiumisoxidizedtohighervalentstateathighertemperature.Theoxygencontentsofnewcompoundsarecalculatedfromtheweightgains.BothV3+andV4+coexistinYSr2-xCaxV3O9-y.Thesecompoundsexhibitlowelectricresistivityatroomtemperature.