简介：一、前言复合材料研究是当代材料科学的最新分支。复合材料有单一材料无法相比的特性与优点:例如高硬度与耐磨性,良好的抗蚀性和特异的装璜效果。国外复合材料工艺已广泛地用于宇航,汽车及其他工业。复合电镀制金属基复合材料始于60年代,其作为表面处理技术它工艺简便,经济,无热处理过程因而不影响工件形状结构,镀层性能优良。例如由复合镀层Ni—Al2O3代镀硬Cr,不仅成本低性能优良,而且可免除Cr对环境的污染。因此近年来我国

简介：HydrotalciteprecursorsofLamodifiedNi-Al2O3andNi-SiO2catalystspreparedbyco-precipitationmethodandthecatalyticactivitieswereexaminedfortheproductionofCOx-freeH2byCH4decomposition.Physico-chemicalcharacteristicsoffresh,reducedandusedcatalystswereevaluatedbyXRD,TPRandO2pulsechemisorptions,TEMandBET-SAtechniques.XRDstudiesshowedphasesduetohydrotalcite-likeprecursorsinovendriedformproduceddispersedNiOspeciesuponcalcinationinstaticairabove450C.Ramanspectraofdeactivatedsamplesrevealedthepresenceofbothorderedanddisorderedformsofcarbon.Ni-La-Al2O3catalystwithamoleratioofNi:La:Al=2:0.1:0.9exhibitedtremendouslyhighlongevitywithahydrogenproductionrateof1300molH2mol1Ni.AdirectrelationshipbetweenNimetalsurfaceareaandhydrogenyieldswasestablished.

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：Thecorrosionbehaviorandanti-corrosionmechanismoftheZn-Ni-Al2O3compositecoatingwereinvestigatedbySEM,EDSandXPS.TheresultsindicatethatthecorrosiontypeoftheZn-Ni-Al2O3coatingsinneutral5wt.%NaClsolutionisuniformcorrosion.ThepresenceofcompactanduniformlydispersednanoaluminaparticlessubstantiallyinhibitsthecorrosionofZn-Ni-Al2O3compositecoatings.Intheinitialcorrosionstage,thecorrosiveproductsofZn-NimatrixformacompactZnCl2·4Zn(OH)2layer.Withthedevelopmentofcorrosion,somenanoaluminaparticlesareembeddedandformaNienrichmentlayer.InNienrichmentlayer,NipresentsasNiandNiO.

简介：

简介：Nanosheet(S)andnanoplate(P)γ-Al2O3weresynthesizedbysimplehydrothermalmethodsandemployedassupportsforNicatalystsinCO2methanation.BothofthenanostructuredNi/Al2O3catalystsdisplayedgoodactivity.Incomparison,theNi/Al2O3-ScatalystshowedhigherCO2conversionthantheNi/Al2O3-Pcounterpartatthereactiontemperaturerangingfrom250to400°C.ThephysicalandchemicalpropertiesofthecatalystsweresystematicallycharacterizedbyN2sorption,X-raydiffraction(XRD),highresolution-transmissionelectronmicroscopy(HR-TEM),hydrogentemperature-programmedreduction(H2-TPR)andCO2temperature-programmeddesorption(CO2-TPD)techniques.Higherspecificsurfaceareaandstrongermetal-supportinteractionswereconfirmedontheNi/Al2O3-Scatalyst,whichmayleadtosmallerparticlesizeofNinanoparticles.Moreover,theNi/Al2O3-Scatalystpossessedmoreabundantweakandmediumbasicsites,whichwouldbenefittheactivationofCO2.ThesmallerNisizeandmoresuitablebasicsitesmayrationalizethesuperioractivityoftheNi/Al2O3-Scatalyst.Besides,theNi/Al2O3-Scatalystexhibitedexcellentstabilityat325°Cfor40h.

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：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：ThemorphologyandcorrosionbehaviorofNi/Al2O3compositecoatingspreparedusingdouble-pulsedelectrodepositingtechniqueafteroxidizedunder800℃NaCldepositinairenvironmentwereanalyzedbyscanningelectricalmicroscope(SEM),X-raydiffraction(XRD)andenergydispersivespectrum(EDS).TheresultsshowedthatthecorrosionofallcompositecoatingswasacceleratedunderNaCldeposits,andthecorrosionproductswereratherporouswithpooradherencetothematrix.Al2O3particlesinthecoatingscanrefinethegrainsizeandimprovethehightemperaturecorrosionresistanceofthecoatings.Withinthetestscope,themoreAl2O3particlesinthecoatings,thelowercorrosionratescouldbeobtained,andthecorrosionmechanismwasalsodiscussed.

简介：Thispaperreportsonthelongevityofglycerol-dry(CO2)reformingoverthelanthanum(La)promotedNi/Al2O3catalysts.TheXRDresultsshowedthattheNiparticlewaswell-dispersedinthepresenceofLapromoter.Inaddition,viatheNH3-TPDanalysis,itwasfoundthattheLapromoterhasreducedtheacidityofNicatalystwhichmayhaveexplainedthemitigationofcarbonlaydown.Itwasdeterminedthatthe3.0wt%La-promotedNi/Al2O3catalystpossessedthelargestBETspecificsurfaceareaof97m2g-1.Consequently,ityieldedthebestcatalyticlongevityperformancewithconversionattainedmorethan90%,evenafter72hofreactionduration.Significantly,itcanbeconfirmedthatthepresenceofCO2duringtheglyceroldryreformingwasessentialinreducingcarbondeposition,mostlikelyviagasificationpathway.Thishasensuredastabilityofcatalyticactivityforalongreactionperiod(72h).

简介：介绍了电刷镀Ni、n—Al2O3／Ni镀层在海水中静态腐蚀400h后的质量损失情况。用扫描电镜（SEM）和能谱仪（EDS）分别观测了腐蚀形貌及进行了成分分析，又在加速腐蚀状态下测试了极化曲线。初步分析得出：Ni可以和未配对的电子的氧形成强的化学键，也可以和基体铁形成微观腐蚀电池；电刷镀n—Al2O3／Ni镀层比Ni镀层在海水中静态耐蚀性好。

简介：

简介：TheZrO2-Al2O3ceramiccompositeswerepreparedbyappropriatetechniqueswithcommercialZrO2andAl2O3powdersasrawmaterialsandY2O3asstabilizer.TheresultsindicatethatwiththeintroductionofAl2O3intotheZrO2matrixwherethequantityofadditiveY2O3is3.5%(molefraction),thegrowthofZrO2grainsisefficientlyinhibited,whichhelpstheZrO2grainsexistinametastabletetragonalmanner;thushigherstrengthandtoughnessareacquired.Whenthecontentofaluminais20%(massfraction),thebendingstrengthandfracturetoughnessofthecompositesare676.7MPaand10MPa·m1/2respectively,themechanicalbehaviorsareclosetothosepreparedwithZrO2andAl2O3powderssynthesizedthroughwetchemicalapproach.Themechanicalbehaviorsofthecompositesarewellimprovedowingtothedispersiontougheningofaluminagrainsandphasetransformationtougheningofzirconiagrains.

简介：本文制备了Bi2O3-Ni2O3纳米粉末,对其结构进行了表征,并研究了制备的纳米粉末对苯光催化降解的影响因素。结果表明：制备的纳米粉末由Bi2O3和Ni2O3复合而成,经750℃焙烧的光催化剂对苯光催化降解活性最高;水蒸气的加入和氧气的增加,都能促进苯的降解率增大;由Langmuir-Hinshelwood动力学模型得出苯的光催化降解反应的吸附常数和反应速率常数分别为0.1398L·μmol^-1和0.0024μmol·L-1·min^-1。

简介：TheNi-AlalloycontainingCr,FeadditiveswerepreparedasRaneyNiCatalystbyhighenergymilling.ThesizeandsurfacestateofNi-Alalloypowderwerestudiedbyparticlesizeanalyzerandsanningelectronmicroscopy.theStructurewasanalyzedbyXRDandMoessbauermethods.Theresultsshowedthatafterahigh-energymilling(HEM).theNi-Alalloytransformstoanano-scaleNiAlstructurewithrichAl.Byannealingthealloy,ametastableNi2Al3phasecanbeobtained.

简介：

简介：Inthecurrentpaper,dry(CO2)-reformingofglycerol,anewreformingroute,wascarriedoutoveralumina(Al2O3)-supported,non-promotedandlanthanum-promotednickel(Ni)catalysts.Bothsetsofcatalystsweresynthesizedviaawetco-impregnationprocedure.Physicochemicalcharacterizationofthecatalystsshowedthatthepromotedcatalystpossessedsmallermetalcrystallitesize,hencehighermetaldispersioncomparedtothevirginNi/Al2O3catalyst.ThiswasalsocorroboratedbythesurfaceimagescapturedbytheFESEManalysis.Fromtemperature-programmedcalcinationanalysis,thederivativeweightprofilesrevealedtwopeaks,whichrepresentawatereliminationpeakatatemperaturerangeof373to473Kfollowedbynickelnitratedecompositionfrom473to573K.Inaddition,BETsurfaceareameasurementsgave85.0m2g-1forthenon-promotedNicatalyst,whilstthepromotedcatalystsshowedanaverageof1%to6%improvementdependingontheLaloadings.Significantly,reactionstudiesat873KshowedthatglyceroldryreformingsuccessfullyproducedH2.The2%La-Ni/Al2O3catalyst,whichpossessedthelargestBETsurfacearea,gaveanoptimumH2generation(9.70%)ataglycerolconversionof24.5%.

简介：Throughmeasuringthecoefficientoflinearexpansion,thestructureandpropertiesoftheLi2O-Al2O3-SiO2lowexpansionglassceramicscontainingB2O3arestudiedbyJRandXRD.ItisshoutnthattheIRmethodisefficientinthestudyoftheglass-ceramicsstructure.Thereisa"Boronabnormality"inthesystemwhichhasanimportantinfluenceonthepropertiesoftheglass-ceramics.

简介：以超重力场辅助燃烧合成技术制备了呈梯度分布的Y2O3-Al2O3-SiO2玻璃／Y3Al5O12陶瓷梯度复合材料。结果表明，梯度布置两种组分的原料既可防止下层熔体的喷溅，又能提高上层玻璃的透过率。该梯度材料沿超重力方向依次为YAS透明玻璃层、YAS-YAG玻璃陶瓷层和YAG陶瓷层。

简介：BondingofAl2O3tocuisperformeddirectlyusingTifoilattemperatureof1273K.Themicrostructureofthejointinterfaceisinuestigatedthroughscanningelectronmicroscope（SEM）,electron.probemicroanalysis（EPMA）andX-raydiffraction（XRD）.theeffectoftheinitialtifoilthicknessonthereactionlayerthicknessandthejointStrengthareinvestigated.