简介:1IntroductionTherareearthcobaltalloyshavethepotentialformakingthemagneticandmagnetoopticalmaterials.Sofar,therareearthcobaltalloyfilmsaresubstantiallyproducedbysputteringorvacuumplating.Ifsuchfilmsarepreparedbyelectrodepositioninstead,productionefficiencywouldbeimprovedandthecompositionofthealloycouldbecontrolled.Becausetheoxidationreductionpotentialsofrareearthelementsareverynegative,organicsolventsmaybeusedaselectrolyticmedia.ElectrodepositionofGdCoandSmCoinorganicsolutionshasbeenreporte...
简介:采用扩散偶实验方法研究Fe含量对Ti6Al4V合金显微组织和性能的影响。通过制作Ti6Al4V-Ti6Al4V20Fe扩散偶,在1000°C经600h扩散退火,在一个样品内获得具有连续成分梯度的合金。结合电子探针、扫描电镜和纳米压痕,确定Ti6Al4VxFe合金成分-组织-硬度的关系。当合金中Fe含量增加到5%(质量分数)时,时效状态下合金中的α相体积分数降低到55%,同时合金具有最高的硬度,Ti6Al4V5Fe合金将是Ti6Al4VxFe体系中最具前景的合金。HAADF-STEM和XRD结果表明,Ti6Al4V5Fe合金在固溶淬火阶段生成纳米尺寸α''层片,这些亚稳的α''层片在随后的时效过程中逐渐长大,并作为α相的形核核心,形成稳定α相。
简介:ThemixturemodelofAl85Y4Nd4Ni7alloyinwhichapartiallycrystallizedamorphousalloyisregardedasananocompositeofanAlnanoparticleandaremainingamorphousmatrixispresented.Itsevolutionintheprocessofcrystallizationhasbeeninvestigatedbydifferentialscanningcalorimetry(DSC),X-raydiffraction(XRD),andtransmissionelectronmicroscopy(TEM).Mainlyamorphousstructurewithα-Alnanocrystalsembeddedintheamorphousmatrixhasbeenrevealedbymeltspiningthealloy.Crystallizationisshowedtooccurinthreestages:(1)crystallizationofamorphousalloyandformationofAlNiY,AlNdNiandunknowncrystallinephases,(2)formationofAl3YandAl3Nd,and(3)formationofAl3Ni.
简介:采用选晶法在真空定向凝固炉中,制备了C含量分别为0.019%、0.048%、0.074%和0.094%的单晶高温合金,合金表面吹沙后分别在1250、1300℃进行真空热处理,研究不同C含量对单晶高温合金再结晶的影响。结果表明:随着合金中C含量升高,碳化物含量增多,其形态由块状转变为骨架状、发达骨架状;随着C含量增加,合金再结晶层深度无明显变化趋势,这表明碳化物对合金再结晶无明显的抑制作用,随着热处理温度升高,再结晶厚层深度明显增加;C对单晶高温合金再结晶抑制作用与形成碳化物的形态和密度有关,在合金表层形成高密度的碳化物,从而对再结晶晶界形成钉扎作用,阻碍晶界的迁移,能够起到抑制再结晶的作用。
简介:Non-stoichiometriccompoundfluoride-dopedLiFePO4/Ccathodematerialsweresynthesizedviasolid-statereactionusingMgF2andAlF3asdopant.Thefluoride-dopedLiFePO4/CsampleswerecharacterizedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM),transmissionelectronmicroscopy(TEM),andelectrochemicaltesting.TheresultsshowthatthematerialsarewellcrystallizedandfluoridedopingcannotchangethespacestructureofLiFePO4.SlightamountsofFe2O3withnofluorideimpuritywere...
简介:Inthiswork,asimpleandfacileone-potoleylaminesolvothermalsyntheticmethodwasdevelopedtosynthesizeCu_2ZnSnS_4(CZTS)nanocrystals.AndtheCu_2ZnSn(S,Se)_4(CZTSSe)thinfilmswerepreparedbyselenizingCZTSnanocrystals.TheobtainedCZTSnanocrystalsandCZTSSefilmswerestudiedusingX-raydiffraction(XRD),transmissionelectronmicroscopy(TEM),scanningelectronmicroscopy(SEM),energy-dispersiveX-rayspectroscopy(EDX),andultraviolet–visiblespectrophotometer(UV–Vis).TEMresultsshowthatthesphere–likeCZTSnanoparticleswithdiameterbetween12and35nmarepolydispersed.XRDstudiesindicatethatthepreparedCZTSnanocrystalsformkesteritecrystalstructure,andtheCZTSSefilmswithkesteritecrystalstructurearealsoobtainedattheannealingtemperaturesof500and550°C.Inparticularafterannealingat500°Cfor20min,theCZTSSefilmexhibitsasmooth,uniform,crack-free,andlarge-grainedtopographyandpossessesCu-poorandSn-richcomposition.Moreover,itshowsstrongopticalabsorptionfromvisibletonear-infrared(IR)region,anditsopticalbandgap(Eg)isfoundtobeabout1.44eV.
简介:研究Sb元素含量对Sn-Bi系焊料性能的影响。通过差示扫描量热法研究Sn-Bi-Sb焊料的熔化行为。采用铺展实验研究焊料在Cu基板上的润湿性。测试Sn-Bi-Sb/Cu结合界面的力学性能。结果表明:三元合金中含有包共晶反应形成的共晶组织,随着Sb含量的增加,共晶组织增多;在加热速率为5℃/min的条件下,三元合金显示出更高的熔点和更宽的熔程;添加少量Sb对Sb-Bi系焊料的铺展率有影响;在焊料铺展过程中形成反应过渡层,反应过渡层中存在Sb元素而无Bi元素,过渡层厚度随着Sb元素含量的增加而增大。Sn-Bi-Sb焊料的剪切强度随着Sb元素含量的增加而升高。
简介:ToinvestigatethedegradationofcorrosionresistanceofZircaloy-4inLiOHaqueoussolution,SIMS(secondaryionmassspectrometry)analysiswasperformedtoexaminetheprofilesofLi+,K+,andOH-inoxidelayersformedinthesameconcentration(0.1mol/L)LiOHandKOHsolutions.Eventhoughtheoxidelayershaveanequalthickness,thepenetrationdepthofK+isshallowerthanthatofLi+,andthepenetrationdepthofOH-corrodedinKOHsolutionisalsoshallowerthanthatcorrodedinLiOHsolution.ItshowsthatthediffusionofOH-intooxidelayerisaccompaniedbythecorrespondingcation.ThedifferenceofdegradationeffectofLiOHandKOHsolutionsonthecorrosionresistanceofZircaloy-4wasdiscussed.