简介：CeO2nanoparticles(nano-CeO2p)wereaddedintolasercladdedNiCoCrAlYcoatingsonNi-basedsuperalloysubstratetoimprovethemicrostructureandproperties.Scanningelectronmicroscope(SEM),X-raydiffractometer(XRD),micro-hardnesstester,andheattreatmentfurnacewereemployedtoinvestigatetheirmorphologies,phases,micro-hardnessandthermalshockresistance,comparedwiththecoatingwithoutnanoparticlesadded.Theresultsshowedthatthemicrostructureandpropertiesofthecoatingswiththeaddition...

简介：TheAu/CeO2catalystsweresynthesizedbyco-precipitation(CP),deposition-precipitation(DP)andmetalliccolloidsdeposition(MCD)method,andtestedforoxidationofvolatileorganiccompounds(VOCs).ItwasrevealedthattheAu/CeO2catalystpreparedbyDPmethodwasthemostefficientcatalysttowardsthetotaloxidationoftoluene.TheAu/CeO2catalystshadobviouslyhighcatalyticactivity,andthebestresultswasobtainedon3wt.%Au/CeO2catalystpreparedbyDPmethod.Thesecatalystswerechara...

简介：ZnOnanotubeswerehydrothermallysynthesizedandtheZNTs/CeO2fluorescentcompositewerepreparedbyintroducingnanoCeO2particlesintoZnOnano-tubesviaachemicalsolutionadsorptionandannealingprocess.ThesampleswerecharacterizedbyX-raydiffraction,scanningelectronmicroscopy,Fouriertransformationinfraredspectroscopyandroomtemperaturephotoluminescencemeasurement.DuetotheinteractionbetweenCe4+andthesurfaceatomsofZnO2nano-tubes,aphotoluminescenceenhancementwasobser...

简介：CeZr，CeYZr，LaCeZr，LaCePrZr，LaCePrYZr，和LaCePr稳固的答案经由一起沉淀方法被准备，并且借助于X光检查衍射(XRD)和Brunauer-Emmett-Teller(赌注)技术描绘了。稳固的答案的氧存储能力(振荡)被脉搏技术评估，催化活动用一台4隧道催化作用设备被估计。稳固的答案介绍了立方的结构，这被看见。特定的表面区域和热稳定性能被做Y进稳固的答案提高。当做大量La减少了时，做La的小数量在热耐久性上有积极效果特定的表面区域和热稳定性。LaCePrZr和LaCePrYZr固体解决方案用在Nd抽取在特定的表面区域和热稳定性介绍了某个更高的值以后，与LaCePr充实的Baotou稀土元素矿物质残余综合了，当为汽车的经济催化剂用尽纯化，从而启用被过去常。ceria氧化锆固体答案的表面上的涂层Al2O3或SiO2层增加了特定的表面区域和热抵抗。

简介：CeO2-ZeO2稳固的溶液广泛地在当前的汽车的三路的催化剂被用作氧存储倡导者。高热的稳定性组织上性质自从直到1273K的温度被这些材料容易在真实工作条件下面经验丰富，是为实际申请的最重要的要求之一。在现在的纸，我们调查了热水的处理怎么适用于一些做并且ZrO2富有的CeO2-ZrO2先锋可能改进的undoped最后的CeO2-ZrO2稳固的solution.A基本原理的热稳定性被开发那在最后的产品的1273K与热稳定性允许热水地对待的蛋糕的形态学到相互关联，它没取决于混合氧化物的作文。

简介：Theaimofthisresearchistopulseco-depositnano-CeO2particlesintoNi-W-Balloycoatingsinordertoimprovethesurfaceproperties.Theinfluenceofpulsefrequencyanddutycircleondepositionrate,microhardnessandmicrostructures,andtheinfluenceofheattreatmenttemperatureonphasestructures,microhardnessandabrasivityofNi-W-B-CeO2compositecoatingswereinvestigated.Theresultsindicatedthatthepulseco-depositionofnickel,tungsten,boronandnano-CeO2particlefromthebathwhichnano-CeO2particlewassuspendedbyhighspeedmechanicalstirringledtotheNi-W-B-CeO2compositecoatings,possessingbettermicrohardnessandabrasionresistancewhenheat-treatedat400℃for1h.Themicrohardnessas-depositedwith636Hzandthedepositionratewith0.0281mm·h-1wasthehighestatpulsefrequencywith1000Hzandpulsedutycirclewith10%.Microstructuresanalysisdisplaysthatdecreasingpulsedutycycleleadstorefinementingrainstructuresandtheimprovementofmicrostructures.X-raydiffractionshowsthatthecompositecoatingas-depositedwasmainlyintheamorphousstateandpartiallycrystallized,butwhenheattreatedat400℃,thecrystallizationtrendwasstrengthenedfurther.

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.

简介：Loadedonthecordierite,therareearthdopedcompositecatalystwaspreparedbysol-gelmethodcombinedwithdippingtechnique.TakingOrthodichlorobenzeneasmodel,thecatalystwasusedtoremovethedioxinsofthewastegas.Theresultsshowedthatat280℃andgasspacevelocitybeing8000h-1,theorthodichlorobenzenecouldberemovedeffectivilybythepreparedCeO2-TiO2-V2O5compositecatalystwhoseactivitywasremarkablyenhancedbythedopingofCe,whiletheindustrialside-streamtestofdioxinsfromrefuseincinerationsmokeindicatedthatthedecompositionratecouldreachabove93%underthesameconditions.

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：空CuO-CeO2-ZrO2nano粒子被作为反溶剂把甲醇用作溶剂和supercritical二氧化碳与supercritical反溶剂仪器准备。二个关键因素(即，压力和温度)被调查探索催化剂结构和药品化学药品性质的效果(即，形态学，减少的性质，氧存储能力和特定的表面区域)。产生材料与X光检查衍射(XRD)被描绘，高决定传播电子显微镜学(HRTEM)，Brunauer-Emmett-Teller(赌注)，氢温度规划了减小(H2-TPR)和氧存储能力(振荡)测量分别地。试验性的结果证明更低的温度支持了空结构nano微粒的生产。粒子形态学也显著地变化了，即稳固的构造然后首先被转移到空结构回到稳固的建设。为获得空nano粒子的最佳的条件在45点被决定

简介：为水气体移动(WGS)反应的多重金属的催化剂(Ni-Mn-Ce-K/bauxite)被受精准备，并且催化结构和性质被N2调查物理，XRD，H2-TPR，和CO-TPD。结果显示7.5%CeO2的增加显然改进了WGS反应的活动，并且也增加了特定的表面区域和催化剂的毛孔体积。CeO2的增加减少减小温度，提高了H2O的吸附和激活，并且而且改进了公司的吸附内容，活跃地点没被改变，催化剂上的活跃地点的数字没显然增加。

简介：一系列Ni-CeO2催化剂被一起沉淀方法与Na2CO3准备，NaOH，并且混合急躁(Na2CO3:NaOH；1:1比率)同样急躁分别地。催化表演上的precipitants的效果，Ni-CeO2催化剂的物理、化学的性质在X光检查的帮助下被调查衍射(XRD)，Brumauer-Emmett-Teller方法(赌注)，Fourier变换红外线的光谱学(英尺红外)，thermogravimetry(TG)，和H2-TPR描述。Ni-CeO2催化剂为反向的水气体移动反应关于他们的催化表演被检验，并且他们的催化活动是被评价：Ni-CeO2-CP(Na2CO3:NaOH=1:1)>Ni-CeO2-CP(Na2CO3)>Ni-CeO2-CP(NaOH)。相关到特征结果，催化剂由一起沉淀准备了与，这被发现混合急躁(Na2CO3:NaOH；1:1比率)同样急躁氧空缺的大多数数量与高度驱散的Ni粒子伴随了，它做了相应Ni-CeO2-CP(Na2CO3:NaOH=1:1)催化剂展览最高催化的活动。当时Na2CO3或NaOH急躁在Ni-CeO2催化剂导致了更少或没有氧空缺。作为结果，Ni-CeO2-CP(Na2CO3)和Ni-CeO2-CP(NaOH)，催化剂介绍了差的催化性能。

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：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：TheinfluenceofrareearthoxideCeO2onmicrostructureandwearresistanceofM80S20thermalsprayandthermalsprayweldingcoatingsisstudiedusingopticalmicroscope,scanningelectronmicroscope,X-rayenergydispersionspectroscope,X-raydiffractometerandweartestingmachine.Theresultsshowthattheaddi-tionof8%CeO2canimprovethemicrostructure,microhardnessandwearresistanceofcoatingssignificantly.

简介：Ni-W-P-CeO2-SiO2nano-compositecoatingswerepreparedonthecarbonsteelsurfacebypulseco-depositionofnickel,tungsten,phosphorus,nano-CeO2andnano-SiO2particles.Theinfluenceofnano-SiO2particlesconcentrationsinelectrolyteonmicrostructuresandpropertiesofthenano-compositecoatingswereresearched,andthecharacteristicswereassessedbychemicalcompositions,elementdistribution,depositionrate,microhardnessandmicrostructures.Theresultsindicatethatwhennano-SiO2particlesconcentrationsinelectrolytearecontrolledat20g·L-1,thedepositionratewith27.07μm·h-1andthemicrohardnesswith666Hvofthenano-compositecoatingsarehighest,elementlinescanningandareascanninganalysesshowthattheaveragecontentsofelementsW,P,SiandCeinthenano-compositecoatingsareclose,displayingthatthedistributionofeveryelementwithinthenano-compositecoatingsiseven.Anincreaseinnano-SiO2particlesconcentrationsinelectrolyte(whenlowerthan20g·L-1)leadstorefinementingrainstructureofnano-compositecoatings,butwhenitimprovedto30g·L-1,thecrystallitesizesincreaseagainandinthemeantimetherearealotofsmallbosswithnodulationshapeappearingonthesurfaceofnano-compositecoatings.

简介：高度取向附生、纯(001)面向的CeO2电影被激光在SrTiO3(001)底层上种没有任何气体的分子的横梁取向附生方法周围。CeO2的Layer-by-layer取向附生的生长模式被证实由在situ思考高精力的电子衍射(RHEED)观察。高分辨率的X光检查衍射(HRXRD)和高分辨率的传播电子显微镜学(HRTEM)结果显示了STO(100)//CeO2(100)，STO[100]//CeO2[110]为out-of-plane和在里面飞机的取向附生的关系分别地。取向附生的电影的形成机制也根据一个理论模型被讨论。LMBEceria电影的化学状态被评估并且证实因为Ce3+和氧空缺的存在被介绍。

简介：混合氧化物(Ce0.6Zr0.4O2)由帮助微波的加热一起沉淀准备了的CeO2-ZrO2被用作支持经由早期湿的受精的方法与各种各样的CuO内容(0wt.%15wt.%)准备一系列CuO/Ce0.6Zr0.4O2催化剂。获得的CuO/Ce0.6Zr0.4O2样品被N2吸附，XRD，拉曼，TEM和H2-TPR技术，和他们的催化活动描绘因为公司氧化被调查。结果证明CuO/Ce0.6Zr0.4O2催化剂的活动被CuO的内容强烈影响，并且有10wt.%CuO的催化剂在公司氧化展出了最好的催化活动，它能在催化剂被归因于CuO，和高氧空缺集中的高分散和reducibility。

简介：AseriesofCe0.5Fe0.30Zr0.20O2catalystswerepreparedbydifferentmethods(co-precipitationsmethod,citricacidsol-gelmethod,impregnationmethod,physicalmixedmethod,andhydrothermalmethod)andcharacterizedbyX-raydiffraction(XRD),Ramanspectroscopy,Brunauer-Emmett-Teller(BET)andH2-TPRmeasurements.Potentialofthecatalystsinthesootoxidationwasevaluatedinatemperature-programmedoxidation(TPO)apparatus.TheresultsshowedthatalltheFe3+andZr4+wereincorporatedintocerialatticetoformapureCe-Fe-Zr-Osolidsolutionfortheco-precipitationsample,buttwokindsofFephasesexistedintheCe-Fe-Zr-Ocatalystspreparedbyothermethods:Fe3+incorporatedintoCeO2latticeanddispersedFe2O3clusters.ThefreeFe2O3clusterscouldimprovetheactivityofcatalystsforsootoxidationcomparingwiththepureCe-Fe-Zr-OsolidsolutionowingtothesynergeticeffectbetweenfreeFe2O3andsurfaceoxygenvacancies.Inaddition,theactivityofcatalystsstronglyreliedonthesurfacereducibilityoffreeFe2O3particles.HoldingbothabundantfreeFe2O3particlesandhighoxygenvacancyconcentration,thehydrothermalCe0.5Fe0.3Zr0.2O2catalystpresentedthelowestTi(251°C,ignitiontemperatureofsootoxidation)andTm(310°C,maximumoxidationratetemperature)forsootcombustion(withtight-contactbetweensootandcatalysts)amongthefivesamples.Evenafteragingat800°Cfor10h,theTiandTmwerestillrelativelylow,at273and361°C,respectively,indicatinghighcatalyticstability.