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:以无水FeCl,和双硫腙为原料,通过溶剂热法得到分散均匀的棒状含铁前驱体,将该前驱体在400℃煅烧3h后制成管状氧化铁。X射线衍射仪(XRD)和环境扫描电镜(ESEM)的研究结果表明:所得管状氧化铁为六方相(α-Fe2O3,1的一维微米管,其平均直径约为2岬、长度约为10~20μm。傅立叶变换红外光谱仪(FT-IR)所测数据表明,该产物氧化铁表面吸附有部分SO42-离子;而紫外-可见光谱仪(uv-vis)的数据分析发现,其紫外最大吸收k。;约为489nm,带宽吸收约在566.2nm处,间接禁带宽度和直接禁带宽度分别为1.97eV和2.189eV,与文献报道值接近。
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:VariousaffectingfactorsanddegradationmechanismwerestudiedonultrasonicdegradationofmethylorangeadoptingY2O3dopinganataseTiO2catalystpreparedinlaboratory.Intheexperiment,theUV-VISspectrophotometerwasusedtofollowandinspectthedegradationprocessofmethylorange.TheresultsindicatethattheultrasonicdegradationratiosofmethylorangeinthepresenceofanataseTiO2catalystaremuchbetterthanthosewithoutcatalyst.Moreover,thecatalyticperformanceofY2O3dopinganataseTiO2catalystisobviouslyhigherthanthatofanataseTiO2catalystwithoutdoping.TheoptimalconditionswereadoptedinthisworkandthedegradationandCODeliminationratioofmethylorangegotto98%and99.0%in90min,respectively.
简介:为了减少锂离子电池正极材料与电解液的相互作用,用沉淀法在LiNi0.8Co0.2O2表面包覆一层Al2O3,并通过电化学测试、扫描电镜和X射线衍射研究其表面形貌和晶体结构。结果表明,经过表面包覆后,有效地抑制了电解液对正极材料的侵蚀,虽然初始放电容量略有降低,但循环性能明显改善;Al2O3包覆量对LiNi0.8Co0.2O2电化学性能存在影响,包覆量为0.7%(质量分数)的样品性能最优。
简介:以六水合氯化钴(CoCl2·6H2O)和水合三氯化钌(RuCl3·3H2O)为前驱体,采用胶体法制备超级电容器用(RuO2/Co3O4)·nH2O复合薄膜电极材料。用X射线衍射仪以及CHl660C电化学工作站对该复合薄膜的物相结构及电化学性能进行表征。结果表明:当COCl2'6H20和RuCl3·3H2O的物质的量比n(Co):n(Ru)为2:1时,于350℃下热处理2.5h制备的复合薄膜电极具有优良的性能,在浓度为0.5mol/L的H2S04电解液中其比电容达到512F/g,500次充放电循环后比电容量保持在充放电循环前的96.1%;充放电电流为0.01A时,内阻为1.2Ω。
简介:采用喷雾造粒制备Fe2O3空心球团粒,团粒经过氢气还原得到中空Fe颗粒,通过扫描电镜(SEM)观察Fe2O3空心球团粒及其截面的形貌,研究还原时间对Fe颗粒形貌与截面形貌的影响;采用激光衍射粒度分析仪对Fe颗粒进行粒径分析;采用比表面及孔隙度分析仪表征Fe颗粒的比表面积;采用CSM-MCT显微硬度仪测量空心球状Fe颗粒球壁的硬度和弹性模量。结果表明:Fe2O3空心球团粒和Fe颗粒均为多孔中空球状结构,球壁上存在大量微孔,中空孔直径和球颗粒直径的比值在0.4~0.5;在650℃下还原,随着还原时间增加(4,5,6h),球壁晶粒逐步长大,中空球状Fe颗粒的比表面积和粒径逐步减小,球壁趋向致密,硬度和弹性模量提高。
简介:Er~(3+)andLa~(3+)codopedY_2O_3nanocrystallinepowdersweresynthesizedbygelcombustionmethodandcharacterizedwiththermalanalysis,X-raydiffraction(XRD),transmissionelectronmicroscopy(TEM),high-resolutionTEM(HRTEM)techniquesandfluorescencespectroscopy.Afterbeingcalcinedat1200oC,the(Y_(1–x)La_x)_2O_3:Er~(3+)powderswereconfirmedtobecubicY_2O_3phasewiththecrystallinegrainsizeintherangeof20–40nm.TheEr~(3+)emissionat1.53μmfromthe~4I_(13/2)→~4I_(15/2)transitionwasobserved,whichwasfoundtobeenhancedbyintroducingLa~(3+)ions.SuchenhancementcouldbeattributedtotheadjustmentofEr~(3+)ions'localenvironmentbythecodopingofLa~(3+)ions,leadingtotheincreasedgroundstateabsorptioncrosssectionofEr~(3+)ions.
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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: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:Thesinglecrystalofthecomplex[Sc(NO3)3(H2O)2]·(15C5)hasbeenpreparedinacetonitrile.Thenewcomplexhasbeencharacterizedbyelementalanalysis,IRspectra,solubilityandmolarconductancemeasurements.ThestructureofthecomplexisdeterminedbysinglecrystalX-raydiffractionanalysis.
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:Organicsubstancesuchassolventandresin'seffectonluminescentcapabilityofSrAl2O4:Eu2+,Dy3+phosphorwasstudied.Someorganicsolventsandresinswereselectedforexperimentation.TheresultsindicatethatthoseorganicsolventswillnothavenegativeeffectontheappliedcapabilityofSrAl2O4:Eu2+,Dy3+phosphor.Adoptingtheorganicresinsandcoveringmethod,theafterglowluminanceofSrAl2O4:Eu2+,Dy3+phosphorwasincreasedby85.01%and82.51%.