简介:研究了碱性条件下Al3+及碱土金属离子(Mg2+、Ca2+)对H2O2的稳定作用、过渡金属离子Fe3+、Fe2+、Mn2+和Cu2+对H2O2的催化分解作用及MgSO4、DTPA和Na2SiO3对碱性H2O2溶液的稳定作用.结果表明,碱土金属离子Mg2+、Ca2+可以对碱性H2O2溶液起到很好的稳定作用;Al3+在强碱条件下对H2O2的分解没有影响.过渡金属离子Fe3+、Fe2+、Mn2+和Cu2+在碱性条件下都会快速催化分解H2O2.4种过渡金属离子对H2O2的催化分解作用由强到弱依次为:Cu2+、Fe2+、Mn2+、Fe3+.在过渡金属离子存在的情况下,Mg2+仍然有较好的防分解性能;Mg2+对有Fe2+存在的H2O2碱溶液的稳定效果好于Fe3+.无论H2O2的碱性溶液中是否有过渡金属离子,加入DTPA对H2O2均有一定的稳定作用,但其稳定效果远不如添加Mg2+效果好.Na2SiO3加入不含过渡金属离子的碱性H2O2溶液中时,不能够起到稳定H2O2的作用.
简介:A60%Fe/Al2O3catalystwaspreparedbytheco-precipitationmethod.ItwasreducedbyH2toproducemetallicFe,whichwasthensulfidedbyCS2toFe0.96SandFe3S4orphosphidedbytriphenylphosphine(PPh3)inliquidphasestoFe2PandFeP.Itwasfoundthattheironsulfides(Fe0.96SandFe3S4)exhibitedthelowactivityforthehydrodesulfurization(HDS)reactions.TheHDSactivitywasalsolowontheFe(metal)/Al2O3andFe2P/Al2O3catalystssincetheywereconvertedintoFe0.96SandFe3S4duringtheHDSreactions.Incontrast,theFeP/Al2O3wasfoundtobestableandactivefortheHDSreactions.Inparticular,FeP/Al2O3possessedsignificantlysmallerFePparticlesthanFeP/C,leadingtothesignificanthigherHDSactivityofFeP/Al2O3thanFeP/C.
简介:SYNTHESIS AND 183W NMR CHARACTERIZATION OF P4W30Al4(H2O)2O11220- HETEROPOLYANIONSYNTHESISAND183WNMRCHARACTERIZ?..
简介:TheantibacterialeffectofcarryingsilverB2O3-SiO2-Na2Oglassmaterialwasstudiedbymeansofantibacterialring,nephelometery,MICvalue,thinfilmattachmentandmicrocalorimetry,respectively.TheexperimentalresultsoffivekindsofantibacterialtestmethodsarealmostidenticalandcanverifythatcarryingsilverB2O3-SiO2-Na2Oglassmaterialexertsanexcellentantibacterialperformance.Antibacterialringandnephelometeryaresimple,quick,buttheprecisionisrestrictive.MICvalue,thinfilmattachmentmethodandmicrocalorimetrycanquantitativelycomparetheantibacterialeffectsoftheantibacterialglassmaterial.Comparedwiththetraditionalmicrobetestmethods,themicrocalorimetrycananalyzetheinhibitingeffectofthecell'sgrowthandmetabolismontheantibacterialglassmaterialbymonitoringthethermaleffectcontinuouslyandautomatically.
简介:AnO'-Sialon-Al2O3compositerefractorywaspreparedbyinsitureactionofSi3N4-ZrSiO4-Al2O3mixturewithfusedaluminaaggregates.Densification,insitureactionprocedureandmicrostructureofthematerialwereinvestigatedbymeansofX-raydiffraction,opticalandscanningelectronicmicroscopesandEDAX.
简介:Throughmeasuringthecoefficientoflinearexpansion,thestructureandpropertiesoftheLi2O-Al2O3-SiO2lowexpansionglassceramicscontainingB2O3arestudiedbyJRandXRD.ItisshoutnthattheIRmethodisefficientinthestudyoftheglass-ceramicsstructure.Thereisa"Boronabnormality"inthesystemwhichhasanimportantinfluenceonthepropertiesoftheglass-ceramics.
简介:TheZrO2-Al2O3ceramiccompositeswerepreparedbyappropriatetechniqueswithcommercialZrO2andAl2O3powdersasrawmaterialsandY2O3asstabilizer.TheresultsindicatethatwiththeintroductionofAl2O3intotheZrO2matrixwherethequantityofadditiveY2O3is3.5%(molefraction),thegrowthofZrO2grainsisefficientlyinhibited,whichhelpstheZrO2grainsexistinametastabletetragonalmanner;thushigherstrengthandtoughnessareacquired.Whenthecontentofaluminais20%(massfraction),thebendingstrengthandfracturetoughnessofthecompositesare676.7MPaand10MPa·m1/2respectively,themechanicalbehaviorsareclosetothosepreparedwithZrO2andAl2O3powderssynthesizedthroughwetchemicalapproach.Themechanicalbehaviorsofthecompositesarewellimprovedowingtothedispersiontougheningofaluminagrainsandphasetransformationtougheningofzirconiagrains.
简介:ThecorrelationbetweenphasestructuresandsurfaceacidityofAl2O3supportscalcinedatdifferenttemperaturesandthecatalyticperformanceofNi/Al2O3catalystsintheproductionofsyntheticnaturalgas(SNG)viaCOmethanationwassystematicallyinvestigated.Aseriesof10wt%NiO/Al2O3catalystswerepreparedbytheconventionalimpregnationmethod,andthephasestructuresandsurfaceacidityofAl2O3supportswereadjustedbycalciningthecommercialγ-Al2O3atdifferenttemperatures(600–1200C).COmethanationreactionwascarriedoutinthetemperaturerangeof300–600Catdifferentweighthourlyspacevelocities(WHSV=30000and120000mL·g-1h-1)andpressures(0.1and3.0MPa).ItwasfoundthathighcalcinationtemperaturenotonlyledtothegrowthinNiparticlesize,butalsoweakenedtheinteractionbetweenNinanoparticlesandAl2O3supportsduetotherapiddecreaseofthespecificsurfaceareaandacidityofAl2O3supports.Interestingly,NicatalystssupportedonAl2O3calcinedat1200C(Ni/Al2O3-1200)exhibitedthebestcatalyticactivityforCOmethanationunderdifferentreactionconditions.LifetimereactiontestsalsoindicatedthatNi/Al2O3-1200wasthemostactiveandstablecatalystcomparedwiththeotherthreecatalysts,whosesupportswerecalcinedatlowertemperatures(600,800and1000C).ThesefindingswouldthereforebehelpfultodevelopNi/Al2O3methanationcatalystforSNGproduction.
简介:以便得到TiB2-Al2O3的同质的混合物和协议,一个表面修正方法被用来准备nano规模的杂交Al2O3涂的TiB2粒子。PE蜡粒子是第一到由杂交,然后nano规模Al2O3粒子的TiB2粒子上涂又是涂的到由PE蜡粒子涂的TiB2的表面上。SEM,TEM和版本被用来描绘同样收到的核心/壳粒子和它的协议的微观结构。试验性的结果显示出那粒子规模TiB2和Al2O3的同质的分散能不仅在混合粉末而且在使脱蜡的协议被形成。协议当时是由煤气压的sintering(GPS)的sintered。物件顶端的装饰物产品显示出与参考样品由正常方法制作了作比较的改进技工性质。
简介:高温固相反应方法合成了Li1-xNaxMn2O4锂离子电池正极材料。通过Na部分取代锰酸锂中的Li,期待能够弱化Jahn-Teller效应,提高锰酸锂的循环稳定性。实验结果证实了我们的预测。取代量为x=0.06时最佳。