简介:以异丙醇铝为前驱体,HNO3为胶溶剂,采用溶胶-凝胶法制备Al2O3膜。考察HNO3浓度对溶胶及薄膜的影响,通过TG-DTG,XRD,AFM,BET等表征手段对溶胶的稳定性及黏度,薄膜的热稳定性,物相组成,表面形貌,微孔结构及分布等进行综合分析。结果表明:随HNO3浓度增大,溶胶黏度增大,HNO3浓度为5mol/L时溶胶发生团聚;薄膜的热稳定性较好,高于500℃加热薄膜几乎没有质量损失;随烧结温度升高,薄膜中的γ-AlOOH逐渐向γ-Al2O3转变,薄膜因此变得更加稳定;薄膜表面较为平整,微孔分布均匀,平均孔直径为4.22nm。
简介:以邻菲罗啉(Phen)和邻氨基苯磺酸为配体,与硝酸镍利用水热合成法合成标题配合物{[Ni(Phen)3]·L·(OH)}(L=邻氨基苯磺酸阴离子).通过红外光谱和元素分析对标题配合物进行结构表征,X-射线单晶衍射结果表明,标题配合物的分子式为:C42H31O4N7SNi,Mr=788,属单斜晶系,空间群为C2/c,晶胞参数:a=23.119(A),b=15.792(A),c=25.040(A),β=111.2.,V=8523.3(A)3,Z=8,R1=0.0808,ωR2=0.2447.标题配合物由一个配阳离子[Ni(Phen)3]2+,一个邻氨基苯磺酸阴离子和一个氢氧根离子组成.在配阳离子中,中心Ni(Ⅱ)与三个phen分子的六个氮原子配位,形成六配位的八面体构型.配阳离子通过静电引力与阴离子结合.化合物分子间通过氢键和Phen环π-π堆积作用形成三维结构.
简介:在80%Al-20%CuO(质量分数)体系中,通过原位反应法制备Al2O3p-Al复合材料。采用不同方法研究CuO颗粒粒度对复合材料合成温度和显微组织的影响。结果表明,CuO颗粒粒度对Al-CuO体系的完全反应温度有显著影响:含有粒度小于6μmCuO颗粒样品的完全反应温度比含有粒度小于100μmCuO颗粒样品的完全反应温度低200°C。当反应温度低于某一临界值时,原位Al2O3颗粒和Al基体之间不能完全结合;当温度高于某一临界值时,原位Al2O3颗粒的形貌从棒状转变成近球形。这两个临界温度受CuO颗粒粒度的影响:含有粒度小于6μmCuO颗粒样品的临界温度比含有小于100μmCuO颗粒样品的临界温度低100℃。
简介:Theeffectofpromotercobaltandthesequencesofaddingcobaltandmolybdenumprecursorsontheperformanceofsulfur-resistantmethanationwereinvestigated.AllthesesampleswerepreparedbyimpregnationmethodandcharacterizedbyN2-adsorption,X-raydiffraction(XRD),temperature-programmedreduction(TPR)andlaserRamanspectroscopy(LRS).TheconversionsofCOforMo-Co/Al,Co-Mo/AlandCoMo/Alcatalystswere59.7%,54.3%and53.9%,respectively.Amongthesecatalysts,theMo-Co/AlcatalystpreparedstepwiselybyimpregnatingMoprecursorfirstlyshowedthebestcatalyticperformance.Meanwhile,theconversionsofCOwere48.9%forMo/Alcatalystand10.5%forCo/Alcatalyst.TheadditionofcobaltspeciescouldimprovethecatalyticactivityofMo/Alcatalyst.TheN2-adsorptionresultsshowedthatCo-Mo/Alcatalysthadthesmallestspecificsurfaceareaamongthesecatalysts.CoMoO4speciesinCoMo/AlcatalystweredetectedwithXRD,TPRandLRS.Moreover,crystalMoS2whichwasreportedtobelessactivethanamorphousMoS2wasfoundinbothCo-Mo/AlandCoMo/Alcatalysts.Mo-Co/Alcatalystshowedthebestcatalyticperformanceasithadanappropriatesurfacestructure,i.e.,nocrystalMoS2andverylittleCoMoO4species.
简介:Thecorrosionfatiguebehaviorofepoxy-coatedMg–3Al–1Znalloywasinvestigatedinairand3.5wt%NaClsolution.Epoxycoatingasanewmethodwasusedtoimprovethecorrosionfatiguepropertyofthematerial.Resultsshowthatthefatiguelimit(FL)ofthecoatedspecimensishigherthanthatoftheuncoatedspecimensin3.5wt%NaClsolutionbecauseofthestrengtheningandblockingfunctionsoftheepoxycoating.TheFLofthecoatedspecimensin3.5wt%NaClsolutionisashighasthatinair.Itimpliesthatthecoatedspecimensarenotassensitivetotheenvironmentasthemagnesiumalloy.Thelowtensilestrengthandtheshortelongationofthepureepoxycoatingleadtothatthefatiguecrackofthecoatedspecimenisalwaysinitiatedfromtheepoxy-coatingfilmPoresandpinholesacceleratethefatiguecrackinitiationprocess.PinholesarecausedbythecorrosionreactionsbetweentheepoxycoatingandtheNaClsolution.
简介:AseriesofAlx-(Alq3)1-xgranularfilmsispreparedonSiwaferwithnativeoxidelayerusingco-evaporationtechnique.Largelateralphotovoltaiceffect(LPE)isobserved,withanoptimalLPVsensitivityof75mV/mminx=0.35sample.ThedependenceofLPEontemperatureandAlcompositionisinvestigated,andthepossiblemechanismisdiscussed.
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:Throughimprovingtheagingprocessduringsynthesisofthesupport,γ-Al2O3withlargeporevolumeandhighsurfaceareawassynthesizedbyafacilesecondaryreformingmethod.Thesynthesisparameters,suchasthereactiontemperature,thefirstagingtemperatureandthesecondagingtemperature,wereinvestigated.Thetexturalpropertiesofγ-Al2O3werecharacterizedbymeansofN2adsorption-desorptionisotherms,X-raypowderdiffractometry(XRD),scanningelectronmicroscopy(SEM),Fouriertransforminfrared(FTIR)spectroscopyandthermogravimetry(TG).TheexperimentalresultsindicatedthatAACHandamorphousAlOOHweretheprecursorsofalumina,whichwereformedviaprecipitationfromsolutionsafterreactionofaluminumsulphatewithammoniumhydrogencarbonate.Theprecursornanocrystallitesgrewandre-assembledduringthesecondaryreformingprocess,whichresultedinanincreasedporesizeandporevolumeandadecreasedbulkdensity.Theas-synthesizedγ-Al2O3materialsfeaturedmeso/macroporosity,largeporevolume(2.175cm3/g),highsurfacearea(237.8m2/g),andlowbulkdensity(0.284g/mL).
简介:Aseriesofnovelbluelong-lastingphosphorescencephosphorsSr6Al18Si2O37:Eu2+,RE3+(RE3+=Ho3+,Gd3+,Dy3+andPr3+)werepreparedbytheconventionalhigh-temperaturesolid-statereactioninareductiveatmosphere.TheirpropertiesweresystematicallyinvestigatedutilizingX-raydiffraction(XRD),photoluminescence,phosphorescenceandthermoluminescence(TL)spectra.ThephosphorsemittedbluelightthatwasrelatedtotheemissionofEu2+dueto5d-4ftransition.Brightbluelong-lastingphosphorescence(LLP)couldbeobservedaftertheexcitationsourcewasswitchedoff.Fortheoptimizedsample,thebluelong-lastingphosphorescencecouldlastfornearly4hinthelightperceptionofthedark-adaptedhumaneye(0.32mcd/m2).TheeffectsofRE3+ionsonphosphorescencepropertiesofthephosphorswerestudied,andtheresultsshowedthattheco-dopingofRE3+ionsgreatlyenhancedtheintensityofthepeakaround315Kwhichwasrelatedtothelonglastingphosphorescenceofthephosphorsatroomtemperatureandconsequentlyimprovedtheperformanceofthebluephosphorescencesuchasintensityandpersistenttime.
简介:Nano-sizedhexagonalmagnesiumhydroxide(Mg(OH)2)withgooddispersibilitywassynthesizedbyadoubleinjection-hydrothermalmethod,utilizingpolyvinylpyrrolidone(PVP)asanadditiveandwithoptimizedprocessingparameters.SEMandBETanalysisshowedthatthemeanparticlesizeandspecificsurfaceareaoftheMg(OH)2particleswere174nmand50.77m2/g,respectively.TheFT-IRspectraandtheXRDpatternsshowedthatPVPwasadsorbedonthesurfaceoftheMg(OH)2crystal,thuseffectivelylimitingparticleagglomerationandhinderingcrystalgrowthalongthe(101)plane.TGAshowedadecreaseinthedecompositiontemperatureandanincreaseintheweightlossoftheMg(OH)2particlesduetoadditionofPVP.
简介:通过粉末冶金原位合成法制备Al3Ni金属间化合物增强铝基复合材料。采用X射线衍射,扫描电镜,硬度测试和压缩强度测试,研究烧结温度对复合材料微观结构和力学性能的影响。结果表明:在铝基体中成功获得了均匀分布的金属间化合物Al3Ni增强相;随烧结温度从570℃上升到590℃,复合材料的密度从2.435g/cm^-3上升到2.990g/cm^-3,维氏硬度从~24升高到~37;经590℃烧结制备的复合材料表现出了高的压缩强度(255MPa)和伸长率(~40%)。