简介:β-sialon/alumina/silicamixturesweresinteredinflowingnitrogenat1500℃and1600℃respectively.ThesinteringpropertiesandmorphologyofsampleswereinvestigatedbySEM,EDSandXRD.Resultsshowthatsinteredpropertiesofthesamplesareinfluencedbysoakingtemperaturesandcompositions.Bulkdensitiesofsamplesareincreasedwiththeincreaseofthesoakingtemperature,whereastheapparentporositiesaredecreased.Masslossofthesinteredsamplesat1500℃islowerthanthatat1600℃,butallthemasslossremainsapproximatelyconstantwiththeincreaseofsialoncontent.Fromthepointofthermodynamicanalysis,ComplexchemicalreactionstakeplaceinsamplesduringsinteringprocessandthevolatileofSiO(g)isresponsibleforthemasslossofsamples.Comparedtocrosssectionmicrostructureofβ-sialon/Al2O3/SiO2mixturessinteredincokepowderbedconsistingofthedensecenterwithwell-developedcolumnofsialonphase,thetransitionalpartwithneedlelikegrainnitrogen-containingphaseandtheloosepartwithshortgranularAl2O3phase,thoseofmixturessinteredinflowingnitrogenisofwell-developedsialonindensecenterandslightlyloosepartwithsialondebris.
简介:Longlastingstrontiumaluminatephosphorsweresynthesizedbymeansofcoatedprecipitationintheexperiment.SrA12O4monoclinicphasewithlongafterglowwassynthesizedat1100℃withtheaidofH3BO3,andthesynthetictemperaturedecreasedabout100℃-150℃thaninsolidstatereaction.TheprocessofheattreatmentwasstudiedbyTG-DTA.ThephasecompositionsofpowderswereanalyzedbyXRD.ThemicrographsofthesampleswereinvestigatedbySEMandtheluminescentpropertieswereresearchedbyopticalspectrum.TheeffectsofH3BO3onthephasecompositionandmicrostructureofthecalcinedpowderswereinvestigated.TheresultsindicatedthatH3BO3acceleratedtheformationofSrAl2O4byconsumingtheintermediatephase.TheadditionofDy2O3stimulatedtheafterglowpropertyduetotheincreaseinthedepthofthetrapcenterinthematerials.
简介:DBUH-Br3catalyzedselectiveconversionofsulfidestosulfoxidesinthepresenceofH2O2asoxidizingagentisdescribed.Thereactionwasperformedselectivelyatroomtemperatureandrelativelyshortreactiontimes.
简介:MicrostructureandgrainboundarycharacterofhotpressedbinaryAl2O3(mullite,ZrO2)-SiCompositesandquaternaryAl2O3-mullite-ZrO2-SiCcompositewerestudiedbyelectronmicroscopyandmicroanalysis,ResultssuggestthatthereexistgrainboundarysolidsolutionsduetoelementaldiffusionnearSiCandmatrixoxidesgrainboundaries.
简介:TheeffectofyttriaonthesolidreactionmechanismofaCaHPO4·2H2O+CaCO3systematdifferenttemperatureswasexperimentallystud-ied.Thesampleswithandwithoutyttriaweresubjectedtothermogravimetric/differentialscanningcalorimetrymeasurement.ThesampleswereheattreatedatthetemperaturescorrespondingtothepeaksontheDSCspectra,andtheresultedphasecompositionswereidentifiedbyX-raydiffraction.Thetransformationmechanismwasdeducedbycomparingthephasesobtainedatdifferenttemperatures.Theresultsshowthatthetransformationsatbelow1073Karenotaffectedbyyttria,butallthoseatabove1073Karecompletelyaltered.Theformationtem-peratureofhydroxyapatitedecreasesby134K,andthedecompositiontemperatureincreasesby38K.ThepolymorphoustransformationofCa3(PO4)2fromβphasetoαphaseincreasesby47K.Thethermodynamicpropertiesofthetransformationsatabove1073Karealsomodi-fiedbytheadditionofyttria;thatis,theendothermalpeaksaresubstitutedbyexothermalpeaks.
简介:采用丝印法在铝基板上制备具有低室温电阻率、适中热敏常数的负温度系数BaCo0.02ⅡCo0.04ⅢBi0.94O3/Ba0.5Bi0.5Fe0.9Sn0.1O3复合热敏厚膜。采用数字多用表、吉时利2400和阻抗分析仪对热敏厚膜的电学性能进行表征。结果表明:随着Ba0.5Bi0.5Fe0.9Sn0.1O3含量从0.05增加至0.25,厚膜的室温电阻率、热敏常数和峰值电压均有所增加且分别处于1.47-26.5Ω·cm、678-1345K和18.9-47.0V范围内,厚膜峰值电压对应的电流也有所降低且处于40-240mA范围。阻抗谱测试表明,这些热敏厚膜表现出非正常的异质电学微结构行为,由高阻态的晶粒和较低电阻态的晶界区域构成。由此可知,在BaCo0.02ⅡCo0.04ⅢBi0.94O3中添加Ba0.5Bi0.5Fe0.9Sn0.1O3改善了热敏行为但也恶化了电流特征.
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:用微波高温固相法合成了Er^3+单掺Lu2O3,Li^+与Er^3+共掺Lu2O3及Li^+,Zn^2+,Mg^2+掺杂Lu2O3∶Er^3+的荧光粉。实验表明金属离子Li^+、Zn^2+、Mg^2+、Er^3+掺杂Lu2O3,不影响Lu2O3的立方晶相。扫描电子显微镜测量表明,Li^+掺杂可以有效改善粉体的分散性和形貌,Li^+,Zn^2+,Mg^2+共掺杂获得的粉体颗粒分布更加均匀,粒径范围为80~100nm。379nm激发下,Li^+与Er^3+共掺样品发光较单掺Er^3+样品在565nm处的发光增强了4.5倍,而Li^+、Zn^2+、Mg^2+与Er^3+共掺样品较其发光增强5.3倍。980nm激发下,Li^+与Er^3+共掺样品,Li^+、Zn^2+、Mg^2+与Er^3+共掺样品的发光分别比单掺Er^3+样品在565nm处发光增强23倍与39倍,在662nm处发光强度分别增强20倍与43倍。379nm激发下,较单掺Er3+的样品,掺杂Li^+的样品和Li^+,Zn^2+,Mg^2+和Er^3+共掺的样品荧光寿命均有所增加,而Zn^2+、Er^3+共掺及Mg^2+、Er^3+共掺样品的荧光寿命则有所缩短。
简介:(1-x)La_(0.67)Ca_(0.33)MnO_3/Cr_2O_3(LCMO)+xCr_2O_3composites被一个新液相方法综合。XRD和SEM大小表明在LCMO结构和LCMO的晶格常数可溶的很少Cr_2O_3几乎没变化,当大多数Cr_2O_3在谷物边界或在LCMO谷物的表面上是分布式的时。Inresistivity对温度大小,金属--绝缘体转变被观察什么时候x<0.20。抵抗力增加和金属--绝缘体转变温度与Cr_2O_3的增加的内容减少。一个随机的电阻器网络(KRN)模型被使用,到模仿混合样品的运输性质。模拟结果同意试验性的观察。结果证明方法为理解maganite的composites的电子运输是合理的。
简介:利用化学多元醇法合成Gd2O3:Tb^3+纳米粒子,通过对NaOH的加入速率的控制,能将纳米粒子的直径从1-2nm能增大到4nm。利用透射电子显微镜,紫外分光光度计对Gd2O3:Tb^3+纳米粒子的形貌和尺寸、发光进行表征分析。结果表明:分多次加入NaOH比一次性加入NaOH能获得更大尺寸的Gd2O3:Tb^3+纳米粒子。