简介:文章研究了对Mg-9Gd-4Y-0.6Zr合金在时效过程中的微观组织。在225℃时效初期硬度缓慢上升,之后硬度急剧上升,24h出现了明显的时效硬化峰,然后硬度开始下降。微观结构的分析结果表明,在初期(2h)产生了大量弥散分布的具有DO19结构的β″,而在峰值时(24h)出现具有bco的β′,在持续时效(384h)时出现亚稳相β1,而在后来的长时间时效(1000h)时出现既在原位转变的平衡相β。
简介:SinglephaseofBa1-xMgAl10O17:xEu2+(0.02≤x≤0.14)phosphorswasfirstsuccessfullypreparedbyco-precipitationinaqueousmediumwitha'reversestrike'method,usingoxalicacidandammoniatogetherasprecipitants.Completelycrystallizedphosphorswereobtainedat1300℃,whichis300℃lowerthanthetemperatureofsolid-statereaction.TheirphotoluminescencewasinvestigatedunderUVandVUVregion,respectively.TheemissionspectraofBa1-xMgAl10O17:xEu2+samplesexcitedby254or147nmshowedacharacteristicwidebandwiththepeakcentredatabout450~454nm.Optimumemissionintensityreachedatx=0.1andthenconcentrationquenchingoccurred.Thesynthesizedphosphorshows10%higheremissionintensitythanthatpreparedbysolid-statereaction.
简介:Ba0.85Ca0.15Ti0.9Zr0.1O3(BCTZ)lead-freepiezoelectricceramicsco-dopedwithCeO2(x=0.1wt.%,0.2wt.%,0.3wt.%,0.4wt.%,0.5wt.%)andLi2CO3(0.6wt.%)werepreparedbyconventionalsolid-statereactionmethod.InfluenceofCeO2dopingamountonthepiezoelectricproperties,dielectricproperties,phasecompositionandmicrostructureofpreparedBCTZlead-freepiezoelectricceramicsdopedwithLi2CO3wereinvestigatedbyX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM)andotheranalyticalmethods.TheresultsshowedthatthesinteredtemperatureofBCTZlead-freepiezoelectricceramicsdopedwithCeO2decreasedgreatlywhenLi2CO3dopingamountwas0.6wt.%;apureperovskitestructureofBCTZlead-freepiezoelectricceramicsco-dopedwithLi2CO3andCeO2andsinteredat1050°Ccouldalsobeobtained.Thepiezoelectricconstant(d33),therelativepermittivity(εr)andtheplanarelectromechanicalcouplingfactor(kp)ofBCTZceramicsdopedwithLi2CO3increasedfirstlyandthendecreased,thedielectricloss(tanδ)decreasedfirstlyandthenincreasedanddecreasedatlastwhenCeO2dopingamountincreased.TheinfluenceofCeO2dopingonthepropertiesofBCTZlead-freepiezoelectricceramicsdopedwithLi2CO3werecausedby'softeffect'and'hardeffect'piezoelectricadditiveandcausinglatticedistortion.WhenCeO2dopingamount(x)was0.2wt.%,theBCTZceramicsdopedwithLi2CO3(0.6wt.%)andsinteredat1050°Cpossessedthebestpiezoelectricpropertyanddielectricpropertywithd33of436pC/N,kpof48.3%,εrof3650,tanδof1.5%.
简介:一系列Ni-CeO2催化剂被一起沉淀方法与Na2CO3准备,NaOH,并且混合急躁(Na2CO3:NaOH;1:1比率)同样急躁分别地。催化表演上的precipitants的效果,Ni-CeO2催化剂的物理、化学的性质在X光检查的帮助下被调查衍射(XRD),Brumauer-Emmett-Teller方法(赌注),Fourier变换红外线的光谱学(英尺红外),thermogravimetry(TG),和H2-TPR描述。Ni-CeO2催化剂为反向的水气体移动反应关于他们的催化表演被检验,并且他们的催化活动是被评价:Ni-CeO2-CP(Na2CO3:NaOH=1:1)>Ni-CeO2-CP(Na2CO3)>Ni-CeO2-CP(NaOH)。相关到特征结果,催化剂由一起沉淀准备了与,这被发现混合急躁(Na2CO3:NaOH;1:1比率)同样急躁氧空缺的大多数数量与高度驱散的Ni粒子伴随了,它做了相应Ni-CeO2-CP(Na2CO3:NaOH=1:1)催化剂展览最高催化的活动。当时Na2CO3或NaOH急躁在Ni-CeO2催化剂导致了更少或没有氧空缺。作为结果,Ni-CeO2-CP(Na2CO3)和Ni-CeO2-CP(NaOH),催化剂介绍了差的催化性能。
简介:AseriesofSm~(3+)dopedY_2MoO_6werepreparedthroughhightemperaturesolidstatereactiontechnique.Theirphasestructures,morphologiesandluminescencepropertieswereinvestigatedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andphotoluminescencespectrometry.ThemostintenseabsorptionofY_2MoO_6hostoccurredat367nm.EnergytransferfromhostlatticetoSm~(3+)ionscouldbeobserved,andtheschematicdiagramofenergytransferwasconstructed.ThecriticalenergytransferdistanceandenergytransfermechanismbetweenSm~(3+)ionswerediscussedindetail.Consideringthehighcolorpurityandappropriateemissionintensity,Sm~(3+)dopedY_2MoO_6couldbeapromisingphosphorundernearultravioletlightexcitation.
简介:TheinfluenceofrareearthoxideCeO2onmicrostructureandwearresistanceofM80S20thermalsprayandthermalsprayweldingcoatingsisstudiedusingopticalmicroscope,scanningelectronmicroscope,X-rayenergydispersionspectroscope,X-raydiffractometerandweartestingmachine.Theresultsshowthattheaddi-tionof8%CeO2canimprovethemicrostructure,microhardnessandwearresistanceofcoatingssignificantly.
简介:Er3+/Yb3+codopedzincateBaGd2ZnO5phosphorsweresynthesizedviaatraditionalsolidstatereaction.ThecrystalstructureandphasepuritywerecheckedbymeansofX-raydiffraction(XRD),andtheresultsshowedthatpurephaseBaGd2ZnO5phosphorswithvariousEr3+,Yb3+concentrationswereobtained.TheinfluenceofEr3+andYb3+dopingconcentrationsonthegreenandredupconversionemissionswasstudied.Itwasfoundthatbothgreenandredupconversionemissionsunder980nmexcitationweretwo-photonprocessesindependentfromtherareearthdopingconcentrations.However,theupconversionluminescenceintensitiesgreatlydependedontherareearthdopingconcentration.Furthermore,thepopulationprocessesofupconversionluminescenceandthequenchingmechanismswereanalyzed.Thetemperature-dependentgreenupconversionluminescencewasstudied,andthetemperaturequenchingprocessoftwogreenupconversionemissionswasmodeled.Thethermalquenchingprocessesofthegreenupconversionemissionscouldbewellexplainedbythemodelweproposed.
简介:RE-dopedNi-basedcatalystswerepreparedbysol-gelmethod.ThesecatalystswereappliedtothereactionofCO2reformingCH4tosyngas.ThestudiesrevealthatRE-doped(RE=La,Ce,Sm,Yb)Ni-basedcatalystsshowhighercatalyticactivitythanundopedNi-basedcatalyst,andwiththeincreasingofRE-dopedquantity,thecatalyticactivityofcatalystsexhibitsregularchanges.WhenRE-dopedquantityis0.2%(molarratio),thecatalystsshowthebestcatalyticactivity.