简介:Thelargesize,crack-freeZr55Cu30Al10Ni5bulkmetallicglass(BMGs)withthediameterof54mmandtheheightof15mmwasbuiltbylasersolidformingadditivemanufacturingtechnology,whosesizeislargerthanthecriticaldiameterbycasting.Themicrostructure,tensileandcompressivedeformationbehaviorsandfracturemorphologyoflasersolidformedZr55Cu30Al10Ni5BMGswereinvestigated.Itisfoundthatthecrystallizationmainlyoccursintheheat-affectedzonesofdepositionlayers,whichconsistofAl5Ni3Zr2,NiZr2,ZrCu,CuZr2phases.Thecontentofamorphousphaseinthedepositisabout63%.Underthecompressiveloading,thedepositpresentsnoplasticitybeforefractureoccurs.Thefractureprocessismainlycontrolledbytheshearstressandthecompressiveshearfractureanglesofabout39.Thecompressivestrengthreaches1452MPa,whichisequivalenttothatofas-CastZr55Cu30Al10Ni5BMGs,andthereexistvein-likepatterns,river-likepatternsandsmoothregionsatthecompressivefractography.Underthetensileloading,thedepositpresentsthebrittlefracturepatternwithoutplasticdeformation.Thefractureprocessexhibitsnormalfracturemodel,andthetensileshearfractureangleofabout90°.Thetensilestrengthisonlyabout609MPa,andthetensilefractographymainlyconsistsofmicro-scaledcoresandvein-likepatterns,dimple-likepatterns,chocolate-likepatternsandsmoothregions.Theresultsfurtherverifiedthefeasibilityandlargepotentialoflaseradditivemanufacturingonfabricationandindustrialapplicationoflarge-scaleBMGsparts.
简介:基于Mg的氢存储合金MgNi,Mg0.9Ti0.1Ni,和Mg0.9Ti0.06Zr0.04Ni成功地借助于机械alloying(麻省)被准备。结构和这些基于Mg的材料的电气化学的特征被学习。X光检查衍射(XRD)结果证明合金的主要阶段展出非结晶的结构。扫描电子显微镜学(SEM)相片证明Ti和Zr的粒子尺寸代替了合金是在直径的大约24m。合金的周期生活被增加Ti和Zr延长。在50个费用分泌物周期以后,Mg0.9Ti0.06Zr0.04Ni的分泌物能力比MgNi合金的高是91.74%并且37.96%比Mg0.9Ti0.1Ni的高合金。为电极能力腐烂的主要原因是Mg的形成(哦)2(Mg腐蚀的产品)在合金的表面。potentiodynamic极化结果显示做的Ti和Zr在一个碱的答案改进耐蚀。电气化学的阻抗光谱学(EIS)结果建议做的Ti和Zr的那合适的数量显著地改进电气化学的催化活动。
简介:TwonovelwashcoatsCe0.8Zr0.15La0.05OδandCe0.8Zr0.2O2waspreparedbyanimpregnationmethod,whichactedasahostfortheactivePdcomponenttopreparePd/Ce0.8Zr0.15La0.05Oδ/substrateandPd/Ce0.8Zr0.2O2/substratemonolithiccatalystsfortoluenecombustion.ThewashcoatswascharacterizedbyX-raydiffraction(XRD),Ramanspectroscopy,Brunauner-Emmett-Teller(BET),andH2-temperature-programmedreduction(H2-TPR).Theresultindicatedthatboththewashcoatshadstrongvibration-shockresistanceaccordingtoultrasonictest.DopingLa3+intoCeO2-ZrO2solidsolutioncouldgeneratemoreoxygenvacancies,andcouldinhibitthesinterofCeO2-ZrO2solidsolutionwhencalcinedathightemperatures(800,900and1000°C).ThewashcoatCe0.8Zr0.15La0.05Oδhadmuchbetterredoxproperties.ThereductivetemperatureofCe4+speciesshiftedtolowtemperatureby60°Cwhenthewashcoatscalcinedathightemperatures(800,900and1000°C).ThePd/Ce0.8Zr0.15La0.05Oδ/substratemonolithiccatalystcalcinationat500°Chadthebestcatalyticactivityandthe95%tolueneconversionatatemperatureaslowas190°C.Whencalcinedatlowtemperature(500and700°C),thecatalyticactivityhaslittleimprovement,however,whencalcinedathightemperature,thecatalyticactivityofPd/Ce0.8Zr0.15La0.05Oδ/substratemonolithiccatalystshadsignificantimprovement.Ascatalystwashcoat,theCe0.8Zr0.15La0.05OδhadbetterthermalstabilitythanthewashcoatCe0.8Zr0.2O2,thedevelopedPd/Ce0.8Zr0.15La0.05Oδ/substratemonolithiccatalystinthisworkwaspromisingforeliminatingVolatileorganiccompounds.
简介:ThemorphologyandcrystallographyofphasesintheCu-0.12%Zralloywereinvestigatedbyscanningelectronmicroscope(SEM),transmissionelectronmicroscope(TEM),andhigh-resolutiontransmissionelectronmicroscope(HRTEM).Theresultsshowthattheas-castmicrostructureofCu–ZralloyismainlyCumatrixandeutecticstructurewhichconsistofCuandCu5Zrphaseswithafinelamellarstructure.Thedisk-shapedandplatelikedCu5Zrphaseswithfccstructurearefoundinthematrix,inwhichhabitplaneisparallelto{111}aplaneofthematrix.BetweenthecoppermatrixandCu5Zrphase,thereexistsanorientationrelationshipof[112]a||[011]Cu5Zr;(111)a||(111)Cu5Zr.ThespacestructuremodelofCu5Zrphasecanbeestablished.
简介:AZr-1.15wt%Cr-0.10wt%Fealloywasbeta-quenchedfrom1050℃toproduceasupersaturatedα′-phase,andthenheatedforvaryingtimesattemperaturesfrom650℃to760℃toprecipitateZr(CrFe)2.Athermoelectricpower(TEP)techniqueandtransmissionelectronmicroscopy(TEM)wereusedtomonitorthisprecipitationprocess.UsingtheJohnson-Mehl-Avramiequation,theTEPresultsandalineregressionmethod,theactivationenergyfordiffusionandthediffusioncoefficientofchromium(andFe)inα-Zrhavebeencalculatedover650℃~760℃.Thetemperaturedependenceofthediffusioncoefficient,DCr/α(cm2/s)isdescribedat650℃~760℃bytherelationshipformula.ThecoarseningoftheZr(CrFe)2particlesshowsat1/2dependenceofmeanparticlesizeonagingtime,t.Suchatimedependenceistypicalofcoarseningwhereatomtransferacrosstheinterfaceisrate-controlling.
简介:BulkZr55Al10Ni5Cu30metallicglassplateswithadimensionof85mm×35mm×4mmandacomplicatedplatewerefabricatedbyinjectingcastingmethodusingspongyzirconiumandindustrialpurityaluminum,nickelandcopperasrawmaterials.Itwasshownthattheholdingtimeofliquidmetalsatelevatedtemperatureshadagreatinfluenceontheoxygencontentoftheplatesduetothecontaminationresultingfromtheatmosphere.Increasingholdingtimeresultedintheincreaseofoxygencontentintheinjectedalloy.Theglasstransitiontemperaturesofthebulkmetallicglassplatesarehigherthanthatreportedintheliteratureandcrystallizationtemperatureislowerfortheonewithhigheroxygencontentatthesameheatingrate.Theextensionoftheundercooledliquidregion△Txreachingabout87Kis3Khigherthanthatpreviouslyreportedand26Khigherthanthatwithoxygencontentof0.076wtpctfortheonewithoxygencontentashighas0.065wtpct.Thereforetheoxygencontentofthealloyhasasignificantinfluenceontheglassformingabilityandthermalstabilityofbulkmetalglass.Itissuggestedthatdirectcorrelationbetweenhighglassformingabilityandlarge△Txisonlyvalidforawell-definedIowoxygenconcentrationorhastobereconsideredbyincorporatingoxygenasanadditionalalloyingelement.
简介:采用铸锭冶金法制备Al-Zn-Mg-Cu-Zr合金和Al-Zn-Mg-Cu-Zr-Cr-Pr合金,再对其进行均匀化退火(460℃/24h)、锻压、固溶处理—室温水淬及峰时效处理。用金相显微镜观察合金的显微组织,并测试其力学性能,研究复合添加Zr、Cr、Pr对Al-Zn-Mg-Cu超高强铝合金再结晶行为和力学性能的影响。结果表明,复合添加Zr、Cr和Pr可显著抑制Al-Zn-Mg-Cu合金在锻压后回复过程中的亚晶合并长大,使该合金在较高温度(490℃)以及高温长时保温(480℃固溶4h)情况下仍能保持细小的亚晶组织,从而提高合金的力学性能。复合添加Zr、Cr、Pr能使合金在490℃固溶1h后在T6状态下的抗拉强度提高约25MPa、屈服强度提高近30MPa。
简介:TheintermetalliccompoundZr1-xTixCowaspreparedanditssuitabilityforhydrogenstoragewasinvestigated.ThealloysobtainedbymagneticlevitationmeltingwiththecompositionofZr1-xTixCo(x=0,0.1,0.2and0.3,at.%)showsinglecubicphasebyX-raydiffraction.Asingleslopingplateauwasobservedoneachisothermal,andpressure-composition-temperature(PCT)measurementresultsshowthattheequilibriumhydrogendesorptionpressureofZr1-xTixCoalloyincreaseswithincreasingTicontent.Thedesorptiontemperaturesforsupplying100kPahydrogenareabout665,642,621and614KforZrCo,Zr0.9Ti0.1Co,Zr0.8Ti0.2CoandZr0.7Ti0.3Coalloy,respectively.RepeatedhydrogenabsorptionanddesorptioncyclesdonotgenerateseparatedZrCo,TiCoandZrH2phases,indicatingthatalloyshavegoodthermalandhydrogenstabilization.
简介:X-raydiffraction(XRD)anddifferentialscanningcalorimetry(DSC)wereemployedtoinvestigatetheinfluenceofNicontentonthecrystallizationofamorphousZr70Cu30-xNix(atomfrationin%)alloys,ExperimentalresultsshowthatwiththeNicontentincreasingtheactivationenergiesforcrystallizationofamorphousZr70Cu30-xNixalloysincreasecorrespondingly,indicatingthatthethermalstabilityisgreatlyimproved.AlltheDSCtracesofamorphousZr70Cu30-xNixalloysexhibittwoexothermicpeaks,suggestingthatthecrystallizationprocessviaadouble-stageticles,whilethesecondonecorrespondstotheprecipitaionofnano-scaleZr2Niphaseandcrystallizationofresidualamporphousphase,ThemechanismonthecrystallizationofamorphousZr70Cu30-xNixalloyswasdiscussed.
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简介:ByaddingmixtureofZrO2andcarbon,aZr-enhancedcompositecoatingwasproducedontoanAISI1045substratebylasercladding.Themicrostructureandphaseformation,microhardnessandwearresistanceofthecompositecoatingwerestudied.Theexperimentalresultsindicatethatthecompositecoatingwithmetallurgicalbondingtosubstrateconsistsof7-Ni,massiveceramicparticlesofZrC,NiZra,NiTZr〉(Fe,Ni)23C6andF%C.Theinsitu-synthesizedZrCparticlesareuniformlydispersedincompositecoating,whichrefinesthemicrostructureofcompositecoating.WithdifferentZrO2andcarbonaddi-tions,thepropertiesareimproveddifferently.Finally,thefineinsituZrCparticlesimprovethemicrohardnessofcompositecoatingtoHVo.2650,whichisnearly2.7timesthatofNi25coating.Also,thecompositecoatinghasanadvantageinwearresistance;itoffersbetterwearresis-tancewhenmoremixtureofZrO2andcarbonwasaddedinnickelalloys.