简介:ThehotductilityofFe-36NiinvaralloywithdifferentadditionsoftheelementceriumwasinvestigatedusingaGleeble-3800thermal-mechanicalsimulatoroverthetemperaturerange850-1050℃,andtheimprovementmechanismofthehotductilitywasanalyzedusingacombinationofSEM,EDS,andOM.TheresultsindicatedthatFe-36Niinvaralloyexhibitedpoorhotductilitybelow1050℃,whichwasmainlyattributedtoweakgrainboundariesandtheactionofgrainboundarysliding.However,thealloyswithceriumcontentsof0.016%and0.024%bothdemonstratedsubstantialimprovementinthehotductilityovertheentiretestingtemperaturerange.Theobservedimprovementofthehotductilityofthealloywith0.016%ceriumat950℃andthealloywith0.024%ceriumat900℃wasassociatedmainlywiththegrainboundarystrengtheningandtherestrictionofthegrainboundaryslidingbecausetheadditionofceriumreducedthesegregationofsulfuratgrainboundariesandrefinedthegrainstructure.Theoccurrenceandaccelerationofdynamicrecrystallizationwerefoundtoberesponsibleforthehighhotductilityofthealloywith0.016%ceriumat1000℃andthealloywith0.024%ceriumat950-1000℃asaresultoftherefinementofthegrainstructurebyadditionofcerium.
简介:以FeMn合金粉末的形式在铁基合金粉末中添加Mn元素,退火后得到Fe-Cu-Mn部分预合金粉末,采用模壁润滑温压工艺制备Fe-Cu-Mn-C合金,通过对合金密度与硬度的测定以及形貌观察,研究Fe-Cu-Mn-C粉末的压制与烧结行为,以及Mn含量对合金密度和力学性能的影响。结果表明,通过退火处理实现部分预合金扩散而得到的Fe-Cu-Mn粉末具有很好的压制性能,Fe-2Cu-0.5Mn-0.9C压坯密度达到7.37g/cm3,烧结密度为7.33g/cm3;添加适量Mn能有效提升铁基合金的力学性能,其中Fe-2Cu-0.5Mn-0.9C合金的性能最佳,抗拉强度达到715MPa;随Mn含量增加,合金的孔隙增多、密度下降,导致强度和硬度下降。合金的局部氧化对性能产生一定的负面影响。Mn含量对合金组织影响不大,Fe-2Cu-Mn-0.9C合金呈现混合显微组织,由铁素体、珠光体和少量贝氏体构成。Mn的蒸发与凝聚是Fe-Cu-Mn-C的烧结机制。
简介:用溶胶-凝胶法制备镍锌共掺杂Z型锶钴铁氧体Sr3(NiZn)xCo2(1-x)Fe24O41(x=0~0.5)粉末。用X射线衍射(XRD)和扫描电镜(SEM)表征该铁氧体粉末的晶体结构和表面形貌,并测试其室温磁滞回线和室温电阻率。用微波矢量网络分析仪测定该粉末在2~18GHz微波频率范围的复介电常数和复磁导率,根据测量数据计算电磁损耗角正切及微波反射率,分析该材料的微波吸收性能与电磁损耗机理。结果表明:Sr3(NiZn)xCo2(1-x)Fe24O41粉末呈六角片状形貌,晶体结构为Z型,具有良好的软磁特性;x=0.3时该材料的电阻率最低,微波吸收效果最好,在13.5GHz频率的吸收峰为25.1dB,10dB频带宽度为7.7GHz,兼具强的磁损耗和弱的介电损耗。
简介:ThecompoundSm0.98Fe9.02–xGaxNδ(x=0,0.25,0.5,0.75,1)werepreparedbymelt-spunmethodandsubsequentannealingandnitriding.TheRietveldanalysisshowedthatthelatticeexpansionplayedanimportantroleinimprovingtheCurietemperature.AnobviousdevelopmentoftheCurietemperaturewasobtainedwiththeincreasedGacontentfromx=0–1(ΔTc=90oC).Theoptimumcoercivityofnitrideswasobtainedatx=0.25withthevalueHcj=652kA/m(8.15kOe)afterannealing,whichcorrespondedtoareasonabledistributionofgrainsizesofbothTbCu7-typeSmFe9Nδandα-Fe.However,anexcessofGadopingmightleadtoanabnormalgrowthofα-Fe,whichinturndeterioratedthemagneticproperties.ItwasconcludedthatamoderateGacontentwasveryeffectiveinraisingthecoercivityandCurietemperamentintheTbCu7-typeSm-Fe-N.
简介:La15Fe77B8hydrogenstoragealloyswerepreparedusingavacuuminduction-quenchingfurnace.TheresultsofX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM)suggestedthatLa15–xSmxFe2Ni76Mn5B2(x=0,2,4,6)alloyshadmultiphasestructureincludingthemainLaNi5phase,La3Ni13B2phaseand(Fe,Ni)phase.WiththeincreasingsubstitutionofSmforLa,themainphasestructureofalloysdidnotchange,whiletheunitcellvolumesdecreased,thecyclestabilitywasimprovedandthemaximumdischargecapacitydecreased,butthelowtemperaturemaximumdischargecapacityofthesamesubstitutionalloywasgraduallyapproachingthemaximumdischargecapacityatroomtemperature,whichshowedthatLa15Fe77B8hydrogenstoragealloysofthepartialsubstitutionofSmforLahadbetterlow-temperaturedischargeability(LTD).Forthesamesubstitutionalloys,self-dischargecharacteristicsandcyclestabilityatlowtemperaturewerebetterthanthatatroomtemperature.Furthermore,thehigh-ratedischargeability(HRD)andtheexchangecurrentdensityI0firstincreasedandthendecreasedwiththeincreasingofSmcontent,whereasthehydrogendiffusioncoefficientDinalloybulkdecreasedgradually,whichindicatedthatappropriatesubstitutionofSmforLaimprovedtheelectrochemicalkineticspropertiesofthealloys.TheHRDwasmainlydominatedbythecharge-transferrateonthealloysurface.
简介:AseriesofCe0.5Fe0.30Zr0.20O2catalystswerepreparedbydifferentmethods(co-precipitationsmethod,citricacidsol-gelmethod,impregnationmethod,physicalmixedmethod,andhydrothermalmethod)andcharacterizedbyX-raydiffraction(XRD),Ramanspectroscopy,Brunauer-Emmett-Teller(BET)andH2-TPRmeasurements.Potentialofthecatalystsinthesootoxidationwasevaluatedinatemperature-programmedoxidation(TPO)apparatus.TheresultsshowedthatalltheFe3+andZr4+wereincorporatedintocerialatticetoformapureCe-Fe-Zr-Osolidsolutionfortheco-precipitationsample,buttwokindsofFephasesexistedintheCe-Fe-Zr-Ocatalystspreparedbyothermethods:Fe3+incorporatedintoCeO2latticeanddispersedFe2O3clusters.ThefreeFe2O3clusterscouldimprovetheactivityofcatalystsforsootoxidationcomparingwiththepureCe-Fe-Zr-OsolidsolutionowingtothesynergeticeffectbetweenfreeFe2O3andsurfaceoxygenvacancies.Inaddition,theactivityofcatalystsstronglyreliedonthesurfacereducibilityoffreeFe2O3particles.HoldingbothabundantfreeFe2O3particlesandhighoxygenvacancyconcentration,thehydrothermalCe0.5Fe0.3Zr0.2O2catalystpresentedthelowestTi(251°C,ignitiontemperatureofsootoxidation)andTm(310°C,maximumoxidationratetemperature)forsootcombustion(withtight-contactbetweensootandcatalysts)amongthefivesamples.Evenafteragingat800°Cfor10h,theTiandTmwerestillrelativelylow,at273and361°C,respectively,indicatinghighcatalyticstability.
简介:有一般公式的1,10-phenanthroline(phen)的铈,镨和钕的硝酸盐建筑群[行(phen)2(NO3)2(H2O)2]·NO3(在哪儿,Ln=Ce,Pr和Nd)被X光检查晶体学准备并且描绘。这些建筑群的Thermolysis被同时的thermogravimetry(TG)和微分热分析(DTA)调查。等温的TG被拿用模型适合评估运动参数以及为免费isoconversional方法建模。thermolytic小径也被建议,它包含点火跟随的分解。所有三建筑群有第十期协作并且显示出multistep分解。以便评估快速的加热的反应,点火延期(Di)大小被承担。为点火的激活精力被发现在顺序减少:Nd>Pr>Ce。