简介:Thesynthesisofultrafineceriumdioxideprecursorviahomogeneousprecipitationwasstudied.Mixedaqueoussolutionofanhydrousceriumnitrateandureawasfirstheatedto85℃for2h,andthepreparedsuspensionwasthenagedatroomtemperatureforvariousperiodsoftime.Whiteprecipitatewasfinallycollectedbycentrifugingandwashedwithdistilledwaterandanhydrousethanol.Theobtainedceriumdioxide(CeO2)precursorwasobservedwithSEM.Itwasfoundthatthemorphologyandsizeoftheprecursorwerestronglyaffectedbyagingtimeandstirringconditions(withorwithoutstirring).Theprecipitatedfinesphericalparticlesoftheprecursorchangedtheirshapefromellipsetosliceordirectlytoslice.Finesphericalmonodispersed(300nm)precursorpowderscouldbeobtainedbycontrollingtheagingtime.Stirringthesolutionalsocouldchangethereactionprocessandthusthemorphologyandsizeoftheprecursorwerechanged.
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:AnAu/ceria(0.44%,massfraction)catalystcontaininggoldionswaspreparedbyamodifieddepositionprecipitationmethod,andtheevolutionofgoldionsinthecatalystanditsinfluenceonthecatalysisofCOoxidationwereinvestigated.Itwasfoundthattheas-preparedcatalystcontaininggoldionswithhighvalencecouldfullyoxidizeCOat–10°CinitiallybutwasdeactivatedgraduallyatlowtemperaturesduringthereactionwithCOortreatmentbyunpurifiedair.ThedeactivationofthecatalystduringCOoxidationortreatmentofitbyunpurifiedairwasindependentandprogressiveatlowtemperatureswhiletheactivityofthecatalystatrelativelyhightemperatureswasmaintainedwell.DuringthereactionwithCOortreatmentbyunpurifiedair,theXPSresultsindicatethatgoldspeciesevolvedfromhighvalencetolowvalenceandthediffusereflectanceUV-Visspectrashowthathighvalencegoldwasreducedtochargedgoldclusters,goldclustersgrewtosmallgoldcrystalsandsmallgoldcrystalsgrewtolargegoldparticles.Accordingly,thehighvalencegoldcorrespondedtotheactivityatlowtemperaturesandthemetallicgoldwasactiveandrelativelystableathightemperatures.Theturnoverfrequencies(TOF)ofthecatalyststreatedbydifferentmethodsat273Kdecreasedwiththeevolutionofgoldspeciesfromhighvalencetolowvalence,nomaximumofTOFwasobservedalthoughgoldparticlesinthecatalystattainedtoabout2―3nmduringthetreatment.AnAu/ceriacatalystwithagoldloadof0.87%(massfraction)maintainedagoodactivityforCOoxidationwithin18hatroomtemperature.Thecatalystswerecharacterizedviatransmittedelectronicmicroscopy(TEM),inductivelycoupledplasmaopticalemissionspectrometry(ICP-OES),X-raydiffraction(XRD)andBETspecificsurfaceareaandUV-VisDRSaswell.
简介:ThreeseriesofCeO2/CuOsampleswerepreparedbyimpregnationmethodandcharacterizedbyXRD,N2adsorption-desorption,temperatureprogrammedreduction(TPR),XPSandTEMtechniques.IncomparisonwiththesamplespreparedwithCuOasinitialsupport,thesampleswithCu(OH)2asinitialsupporthavehigherreducibilitiesandsmallerrelativeTPRpeakareas,andalsolargerspecificsurfaceareasatcalcinationtemperaturesof400℃–600℃.Asaresult,Cu(OH)2isbetterthanCuOasinitialsupportforpreferentialoxidationofCOinexcessH2(CO-PROX).Thebestcatalyticperformancewasachievedonthesamplecalcinedat600℃andwithanatomicratioofCe/Cuat40%.XPSanalysesindicatethatmoreinterfacelinkagesCe-O-Cucouldbeformedwhenitwascalcinedat600℃.AndtheatomicratioofCe/Cuat40%ledtoaproperreducibilityforthesampleasillustratedbytheTPRmeasurements.
简介:采用无压烧结法制备含CeO2的Mo/Al2O3材料,用MM-200型环-块式摩擦磨损试验机测试该材料在滑动干摩擦条件下的磨损行为,通过X射线衍射(XRD)和电子探针对其微观结构和磨损后的形貌进行研究和分析。结果表明,添加CeO2的烧结样品中出现CeAl11O18相,且随CeO2含量(体积分数)增加,CeAl11O18逐渐增多,Al2O3相应减少。当CeO2的体积分数为6%时Al2O3全部由CeAl11O18取代;CeO2的添加使Al2O3和CeAl11O18相边界处均呈现圆钝形貌,并且存在Mo、Al、O的相互扩散区域。磨损形貌表明,1730℃烧结的样品中出现摩擦转移层,当CeO2含量达到4%时,该摩擦转移层大量出现,从而改善材料的耐磨性。
简介:增加的CeO2(ZrO2)/TiO2催化剂独立由大音阶的第五音胶化和受精的方法准备了的一系列镨为选择催化减小被测试没有,并且由X光检查衍射(XRD)描绘了,N2-brumauer-emmett-teller(N2-BET),NH3-temperature规划了解吸附作用(NH3-TPD),H2-temperature规划了减小(H2-TPR),PL系列,拉曼系列,电子顺磁的回声(EPR)一催化性能上的准备方法的影响被学习。结果证明CeO2(ZrO2)/TiO2催化剂的催化性能上的Pr增加的影响在大音阶的第五音胶化方法和受精方法之间是不同的。Pr增加趋于与TiO2交往并且当它是更可能的与在受精方法形成Ce-O-Pr的结构的CeO2交往时,在大音阶的第五音胶化方法形成了Ti-O-Pr的结构。大音阶的第五音胶化方法准备的催化剂的全部的酸数量和氧化还原作用性质与Pr元素的增加减少了,它导致了催化活动的减少。相反,受精方法准备的增加Pr的催化剂被发现拥有更容易的reducibility,更多的全部的酸数量和Ce3+种类的更高的比例,它为更高催化的活动是赞成的。
简介:当引擎使用与纳米大小的添加剂Ce0.9Cu0.1O2和Ce0.9Zr0.1O2混合的重油时,这篇论文主要在高速度的柴油机引擎和排放减小的表演上学习。在测试期间,Indiset620燃烧分析器由AVL做了,被用来在柱体压力上做即时调查,燃料点火时刻,并且在柱体和曲柄角度建立在温度的变化趋势之间的一种关系。为烧与添加剂混合的重油和重油的引擎,燃烧分析软件Indicom和协奏曲被用来分析它的燃烧进程和排放条件。试验性的调查证明缩放nano的复杂氧化物能改进与重油,和还原剂造成的柴油机引擎的表演象NOx和公司一样的污染物质的排放,把它与纯重油作比较。根据这个实验的后果,添加剂在重油的使用改进全面表演。
简介:摘要 本文通过实验从几个方面考察 Ce2( CO3) 3沉淀、煅烧条件的变化对氧化铈物理性质的影响。当 CeCl3溶液浓度为 140g/l,沉淀时间 60分钟,沉淀温度为 45℃,滤饼洗涤洗水温度 45℃,水洗搅拌 5分钟,澄清 20分钟,水洗 4次, 1000℃煅烧 2小时,可生产符合客户要求标准的 CeO2,即生产的 CeO2松装比重在 0.62~ 0.71g/cm3,比表面积在 2~ 5m2/g。
简介:Ba0.85Ca0.15Ti0.9Zr0.1O3(BCTZ)lead-freepiezoelectricceramicsco-dopedwithCeO2(x=0.1wt.%,0.2wt.%,0.3wt.%,0.4wt.%,0.5wt.%)andLi2CO3(0.6wt.%)werepreparedbyconventionalsolid-statereactionmethod.InfluenceofCeO2dopingamountonthepiezoelectricproperties,dielectricproperties,phasecompositionandmicrostructureofpreparedBCTZlead-freepiezoelectricceramicsdopedwithLi2CO3wereinvestigatedbyX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM)andotheranalyticalmethods.TheresultsshowedthatthesinteredtemperatureofBCTZlead-freepiezoelectricceramicsdopedwithCeO2decreasedgreatlywhenLi2CO3dopingamountwas0.6wt.%;apureperovskitestructureofBCTZlead-freepiezoelectricceramicsco-dopedwithLi2CO3andCeO2andsinteredat1050°Ccouldalsobeobtained.Thepiezoelectricconstant(d33),therelativepermittivity(εr)andtheplanarelectromechanicalcouplingfactor(kp)ofBCTZceramicsdopedwithLi2CO3increasedfirstlyandthendecreased,thedielectricloss(tanδ)decreasedfirstlyandthenincreasedanddecreasedatlastwhenCeO2dopingamountincreased.TheinfluenceofCeO2dopingonthepropertiesofBCTZlead-freepiezoelectricceramicsdopedwithLi2CO3werecausedby'softeffect'and'hardeffect'piezoelectricadditiveandcausinglatticedistortion.WhenCeO2dopingamount(x)was0.2wt.%,theBCTZceramicsdopedwithLi2CO3(0.6wt.%)andsinteredat1050°Cpossessedthebestpiezoelectricpropertyanddielectricpropertywithd33of436pC/N,kpof48.3%,εrof3650,tanδof1.5%.
简介:利用XRD、SEM、显微硬度weibull统计分析以及摩擦磨损试验手段对比研究了等离子喷涂添加ω(TiO2)=13%的TiO2的AlO3涂层(以下简称AT13涂层)和添加不同含量CeO2的AT13涂层的微观组织和性能。研究表明,CeO2以铺展良好的薄片状分布于涂层中,有效改善了涂层中层片之间结合。稀土CeO2的添加不改变AT13相变规律。涂层显微硬度的Weibull统计分析表明,添加CeO2对AT13涂层的显微硬度影响不大,显微硬度分布的分散性降低。当ω(CeO2)=4%时,涂层显微硬度分布的分散性最小。AT13材料中添加CeO2可显著提高涂层的耐磨性,当ω(CeO2)=8%时,涂层的耐磨性最好。添加CeO2不改变涂层的磨损机制,但显著降低涂层的磨损剥落程度。