简介:在situcomposites在艾尔矩阵上研究严重塑料变丑的影响规则,10?wt%艾尔3在situ的Zr/2024Al增强粒子合成被准备由直接融化反应(DMR),然后,合成是由有90的一个方向的热伪造?%塑料变丑。然后,前进状态的微观结构合成被观察,并且机械性质的变化法律和磨擦表演在以后并且在塑料使变形前被比较。结果显示艾尔3增强Zr的粒子旋转并且闯入10-20的更小的尺寸?ng可溶的biopolymer有三个转变金属离子的牛的浆液白朊(BSA)(M,M=Cu,公司,Mn)。白朊一定的金属离子的有约束力的模式和比率被调查。BSA-M建筑群被紫外力的、圆形的二色性(CD)描绘系列和polyacrylamide胶化电气泳动(页)。当聚合物支架和金属建筑群作为催化活跃中心工作了,BSA服务了。当到BSA的转变金属离子建筑群的有约束力的比率是5:1时,结果证明BSA的结构仍然保持未改变。而且,清除superoxide阴离子自由的基(O\(_{2}^{\bullet-}\??
简介:HotcompressionbehaviorofTiC–Al2O3/AlcompositeswasstudiedusingtheGleeble-1500systematatemperaturerangeof300–550°Candatstrainraterangeof0.01–10.00s-1.TheassociatedstructuralchangeswerestudiedbyTEMobservations.Theresultsshowthatstressleveldecreaseswithdeformationtemperatureincreasingandstrainratedecreasing,whichcanberepresentedbyaZener–Hollomonparameterinanexponent-typeequationwithhotdeformationactivationenergyQof172.56kJ·mol-1.Dynamicrecoveryoccurseasilywhenstrainratesarelessthan10.00s-1.Dynamicrecrystallizationcanoccuratstrainrateof10.00s-1.
简介:BondingofAl2O3tocuisperformeddirectlyusingTifoilattemperatureof1273K.Themicrostructureofthejointinterfaceisinuestigatedthroughscanningelectronmicroscope(SEM),electron.probemicroanalysis(EPMA)andX-raydiffraction(XRD).theeffectoftheinitialtifoilthicknessonthereactionlayerthicknessandthejointStrengthareinvestigated.
简介:Al-3B中间合金是亚共晶Al-Si合金的高效细化剂之一。实验研究了Al-3B中间合金中未溶AlB2颗粒对Al-7Si合金晶粒细化的影响。结果表明,AlB2颗粒的数目和沉降对晶粒细化效果都有重要影响。在实验结果和理论分析基础上,提出了Al-3B中间合金对亚共晶Al-Si合金晶粒细化的新机制,认为通过共晶反应形成的"Al-AlB2"包覆结构是导致晶粒细化的直接原因,未溶的AlB2颗粒是α(Al)相的间接行核基底。
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:晶体结构和加氢行为(La_(1-x)Mg_x)_3Al(x=0.1,0.2,0.3,和0.4)合金被调查。这被发现有x=的合金0.1La和第0.2consi(Mg,艾尔),La,和一个新奇阶段。新奇阶段作为La_2Al被决定。当Mg满足增加,La_2Al的数量减少,这被显示出。当x增加到0.3时,onlyLa(Mg,艾尔)并且La_2Al的小数量存在。当x是0.4时,La_2Al阶段消失,合金包含两La(Mg,艾尔)并且La(艾尔,Mg)_2洗阶段。(La_(0.9)Mg_(0.1))_3Al并且(La_(0.7)Mg_(0.3))_3Al合金能被氢的吸收在473K分解成LaH_3,MgH_2,和La_2Al_5。
简介:ThispaperintroducesabrazingprocessbetweenAl_2O_3ceramicandInvaralloy.Al_2O_3canbebrazedwithInvareffectively.TheinterfacialstructureofAl_2O_3/Invarjointcanbeexpressedas:Invar/Ag(s,s)+Cu(s,s)+Fe_2Ti(zoneⅠ)/Ag(s,s)+Cu(s,s)+Fe_2Ti+NiTi+Cu_3Ti(zoneⅡ)/Ag(s,s)+Cu(s,s)+Cu_2Ti+Al(s,s)+TiC+TiO(zoneⅢ)/Al_2O_3.Themaximumshearstrengthof139MPawasmeasuredforas-brazedAl_2O_3/Invarjointbrazedat850℃for25minor900℃for15min.
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:TheeffectofAl-3Ti-0.2C-5Sr(wt%)grainrefinerontherefiningperformanceandmodificationofA356alloywasinvestigatedusingopticalmicroscope(OM).ThemorphologyandcrystalstructureofternaryAl-Ti-SrphasesinAl-3Ti-0.2C-5Srrefinerwereanalyzedbyscanningelectronmicroscopy(SEM)andtransmissionelectronmicroscopy(TEM).TheresultsshowthattheternaryAl-TiSrphasesinAl-3Ti-0.2C-5SrrefinercanpromotethegrainrefiningefficiencyofA356alloy.TheternaryAl-Ti-Srphasesco-existintwomorphologies,i.e.,blocky-likephaseandsurround-likephase,besides,whichbothhavethesamechemicalcompositionofAl_(34)Ti_3Sr.ThecrystalstructureofAl_(34)Ti_3Srisface-centeredcubic,andthelatticeparameterisdeterminedtobeabout1.52nm.
简介:钛酸铝系复合材料中钛酸铝的体积分数不同,会导致Al2TiO5/Al2O3复合材料的抗铝液浸渗性能的不同。在Al2TiO5中分别按10%、20%、40%、60%、80%、90%(体积分数)引入Al2O3进行复合。通过对渗铝试样的外观形貌、微观结构分析,进而对其铝液浸渗性能进行了分析比较,发现富钛酸铝的钛酸铝/氧化铝复合材料(妒(AL2TiO5)〉40%)抗铝液浸渗性能好;而富氧化铝的钛酸铝/氧化铝复合材料(φ(Al2TiO5)〈20%)有金属铝液沿热震产生的裂纹渗入复合材料内部,容易导致复合材料断裂失效。该研究结果对可靠应用钛酸铝系复合材料作为铝液的容器具有实际工程应用价值。
简介:为了开发新型高阻尼金属基复合材料,以高温烧结后的大晶粒钛酸钡(BaTiO3)陶瓷作为增强体,通过粉末冶金和热挤压方法制备钛酸钡颗粒增强铝基复合材料,并研究其阻尼特性和力学特性。动态力学分析结果表明,大晶粒钛酸钡陶瓷本身具有很好的阻尼性能,阻尼值可达0.12。但在纯铝基体中加入质量分数为10%BaTiO3制备的BaTiO3/Al复合材料的室温阻尼性能和铝基体相比并无明显改善,而450K以上的阻尼性能由于界面附近的位错运动而大幅度提高。钛酸钡增强体的本征阻尼性能未能充分发挥的原因在于钛酸钡颗粒与铝基体之间的界面结合不良,导致钛酸钡颗粒内部的能量耗散机制无法触动。复合材料的拉伸性能比相应纯铝基体的提高了42%,这意味通过改善界面结合和加入高含量的碳酸钡阻尼增强颗粒,有望获得高强度高阻尼金属基复合材料。
简介:Thecorrosionfatiguebehaviorofepoxy-coatedMg–3Al–1Znalloywasinvestigatedinairand3.5wt%NaClsolution.Epoxycoatingasanewmethodwasusedtoimprovethecorrosionfatiguepropertyofthematerial.Resultsshowthatthefatiguelimit(FL)ofthecoatedspecimensishigherthanthatoftheuncoatedspecimensin3.5wt%NaClsolutionbecauseofthestrengtheningandblockingfunctionsoftheepoxycoating.TheFLofthecoatedspecimensin3.5wt%NaClsolutionisashighasthatinair.Itimpliesthatthecoatedspecimensarenotassensitivetotheenvironmentasthemagnesiumalloy.Thelowtensilestrengthandtheshortelongationofthepureepoxycoatingleadtothatthefatiguecrackofthecoatedspecimenisalwaysinitiatedfromtheepoxy-coatingfilmPoresandpinholesacceleratethefatiguecrackinitiationprocess.PinholesarecausedbythecorrosionreactionsbetweentheepoxycoatingandtheNaClsolution.
简介:以MoO3粉、Mo粉、Si粉及Al粉为原料,采用机械合金化法合成了纳米Mo5Si3-20%Al2O3(质量分数)复合粉体。采用XRD、SEM、TEM和DTA等对复合粉体在球磨过程中结构变化进行了研究。结果表明:球磨10h后合成的Mo5Si3-20%Al2O3复合粉体,反应以爆炸模式进行。球磨30h后,Mo5Si3和Al2O3的晶粒尺寸分别为36.3nm和21.9nm。随着球磨时间的延长,Mo5Si3和Al2O3的晶粒尺寸变小,衍射峰宽化程度降低。DTA和XRD分析结果表明,复合粉体具有好的热稳定性,球磨30h后再在1000℃退火1h后复合粉体没有发生物相转变。更多还原
简介:Fe3AlandCr18-Ni8steelwerebondedinvacuumandaninterfacewasformedbetweenFe3AlandCr18-Ni8steel.Stressdistributionatthediffusion-bondedinterfacewasresearchedbynumericalsimulationandfiniteelementmethod(FEM).TheresultsindicatedthatthepeakstressappearedattheinterfacenearCr18-Ni8steelside.Thisisthekeyfactortoinducecrackatthisposition.Withtheenhancementofheatingtemperature,thepeakstressatthebondedinterfaceincreases.Whenthetemperatureis1100℃,thepeakstressisupto65.9MPa,whichisbiggerthanthatat1000℃by9.4%.Inaddition,thepeakstressbecomesbiggerwiththeincreaseofthethicknessofbasemetalfrom1mmto8mm.Whilethethicknessismorethan8mm,thepeakstressvariesslightlywiththechangeofthethickness.
简介:Mg–9Li–3Al–1.6Yalloyswerepreparedthroughmixturemethod.Themicrostructure,mechanicalproperties,andcorrosionresistanceoftheas-castandasextrudedalloyswerestudiedbyopticalmicroscopy(OM),scanningelectronicmicroscopy(SEM),X-raydiffraction(XRD),mechanicalpropertiestesting,andelectrochemicalmeasurement.Theas-castMg–9Li–3Al–1.6Yalloywiththeaveragegrainsizeof325lmiscomposedofb-Limatrix,blocka-Mg,andgranuleAl2Yphases.Afterextrusion,thegrainsizeoftheas-castalloyisobviouslyrefinedandreachesto75lm;thestrengthandelongationoftheextrudedalloyareenhancedby17.20%and49.45%,respectively,owingtotheirfinemicrostructureandreductionofcastingdefects.Theas-extrudedalloyshowsbettercorrosionresistancecomparedtotheas-castone,whichmayberelatedtothelowstoredenergyanddislocationdensityintheextrudedalloy,alsothehomogenizationtreatmentbeforeextrusion.
简介:Au/-Al2O3催化剂被免职降水方法为低集中白酒溪流(甲醇,乙醇,iso-propanol和n-propanol)的催化燃烧作好准备。催化剂被X光检查光电子描绘光谱学(XPS),X光检查diffractometry(XRD)和精力散X光检查微分析(版本)技术。XPS结果证明仅仅催化剂的表面上有Au0。XRD模式证明Au高度大概在-Al2O3上被驱散。为有2.0g/m3的集中的甲醇,乙醇,iso-propanol和n-propanol的完全的变换的温度是60,155,170和137?,分别地但是他们完全在60,220,260和217点被使矿物化进CO2和H2O吗?分别地在优化催化剂上。催化剂的活动在130h是稳定的。为催化甲醇消除的动力学跟随了伪--首先订表示为r=0.6528c0+0.084的反应2。明显的激活精力的价值是在反应温度的范围的54.7kJ/mol。
简介:ThedistributionsoftheaxialstressandshearstressinAl2O3-TiC/Q235diffusionbondedjointswerestudiedusingfiniteelementmethod(FEM).Theeffectofinterlayerthicknessontheaxialstressandshearstresswasalsoinvestigated.Theresultsindicatethatthegradientsoftheaxialstressandshearstressaregreatnearthejointedge.ThemaximalshearstressproducesattheinterfaceoftheAl2O3-TiCandTiinterlayer.WiththeincreaseofCuinterlayerthickness,themagnitudesoftheaxialstressandshearstressfirstdecreaseandthenincrease.Thedistributionoftheaxialstresschangesgreatlywithalittlechangeintheshearstress.TheshearfractureinitiatesattheinterfaceoftheAl2O3-TiC/TiinterlayerwithhighshearstressandthenpropagatestotheAl2O3-TiCside,whichisconsistentwiththestressFEMcalculatingresults.