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ID:23802962
大小:4.26 MB
页数:107页
时间:2018-11-10
《氧化物及金属包覆镁基超细粉制备与储氢性能研究》由会员上传分享,免费在线阅读,更多相关内容在教育资源-天天文库。
1、上海交通大学硕士学位论文alloybulkto0.58wt%intheevaporatedMg-Ypowder,whiletheCecontentjustreduced5wt%intheMg-Cemixtureanodeto2.92wt%inthearcevaporatedMg-Cepowder.ComparedtheMg-CeoxidepowderwithMg-Y2O3powderonhydrogenabsorptionanddesorptionperformances,thehydrogena
2、bsorptionactivationenergyoftheMg-Ceoxide(47.75kJ/molH2)islowerthantheMg-Y2O3(79.9kJ/molH2).DTAcurvesshowthattheonsethydrogenreleasetemperaturewas658KforthehydrogenatedMg-Ceoxidepowder,whichislowerthanthat(676K)ofMg-Y2O3powder.TheseresultsrevealedthatC
3、e2O3hasbettercatalyticeffectonMg-basedhydrogenstoragematerialsthanY2O3.ThestudyofmetalcoatedpureMgultrafinepowdersshowthat:themetalsgeneratedfromtheelectrolessplatingcoveredonthesurfaceofMgparticlesandformedacore-shellstructure.TheMg@Nicompositehasexc
4、ellentperformanceonhydrogendesorptionproperties.DSCcurveofthehydrogenatedMg@Nishowsanonsethydrogenreleasetemperatureof616KandthelowestPCTrecyclingtemperatureis548K.Mg2NiplaysthecatalyticrolefortheMg@Nicomposite.FortheMg@Fepowder,theonsethydrogenreleas
5、etemperatureandhydrogenabsorbingactivationenergyare623Kand56.39kJ/molH2,respectively.AsMgFe2H6isnot foundinthehydrogenatedMg@Fesample,whichmeansFeshellisthe actualcatalyst.ThehydrogendesorptionabilitiesofMg@Tipowderare similartotheMg@Nipowder.TheDSCcu
6、rveofhydrogenatedMg@Ti showsanonsethydrogenreleasetemperatureof620KandthelowestPCT recyclingtemperatureis548K.TiandTiO2depositedonMgparticle surfacesimultaneouslyduringelectrolessplating,bothshowgoodcatalytic effectonthedehydrogenationperformanceofMgH
7、2.Keywords:DCarcplasma,Mg-basedhydrogenstoragematerials,electrolessplating,coatingIV万方数据上海交通大学硕士学位论文目录摘要.................................................................................................................................IABSTRACT.........
8、..........................................................................................................III第一章绪论....................................................................................................................11.1氢能源开发的意义及
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