简介:Pt(Ⅱ)andPd(Ⅱ)complexeswith2',3',4',5,7-pentahydroxy-flavoneweresynthesizedandcharacterizedbyelementalanalysis,molarconductance,IR,1HNMR,TG-DTA,UV-Visspectroscopictechniques,andfluorescenceanalysis.Thescavengingeffectonthesuperoxideradical(O-2)andtheinhibitoryeffectonlipidperoxideswerealsoinvestigated.Boththeligandandthecomplexesexhibitscavengingeffectonsuperoxideradicals,andtheeffectofthecomplexesisgreaterthanthatoftheligand.ThePt(Ⅱ)complexexhibitsthestrongestscavengingefficiency.BothPt(Ⅱ)andPd(Ⅱ)complexeshavetheinhibitoryeffectonlipidperoxides,andtheeffectofthecomplexesisgreaterthanthatoftheligand,butthePt(Ⅱ)complexhasahigheffectofpromotinglipidperoxides.
简介:TheelectronicstructuresofspinelMgAl2O4andMgOtunnelbarriermaterialswereinvestigatedusingfirst-principlesdensityfunctionaltheorycalculations.OurresultsshowthatsimilarelectronicstructuresarefoundfortheMgAl2O4andMgOtunnelingbarriers.ThecalculateddirectenergygapsattheΓ-pointareabout5.10eVforMgAl2O4and4.81eVforMgO,respectively.BecauseofthesimilarfeatureinbandstructuresfromΓhigh-symmetrypointtoFpoint(△band),thecoherenttunnelingeffectmightbeexpectedtoappearinMgAl2O4-basedMTJslikeinMgO-basedMTJs.ThesmalldifferenceofthesurfacefreeenergiesofFe(2.9J.m-2)andMgAl2O4(2.27J·m-2)onthe{100}orientation,andthesmallerlatticemismatchbetweenMgAl2O4andferromagneticelectrodesthanthatbetweenMgOandferromagneticelectrodes,thespinelMgAl2O4cansubstituteMgOtofabricatethecoherenttunnelingandchemicallystablemagnetictunneljunctionstructures,whichwillbeappliedinthenextgenerationreadheadsorspintronicdevices.
简介:微观结构和形成的激光固体(LSF)的机械性质上的热处理的效果Ti-6Al-4V合金被调查。温度的影响和答案处理和老化处理的时间被分析。结果证明LSFed样品的微观结构与300μm的平均谷物宽度由Widmanstättenα板条和在圆柱的优先的β谷物针状的一些组成,它沿着免职方向(Z)从底层取向附生地成长。解决方案处理在处理主要影响的主要、第二等的α板条,和老化的宽度,方面比率,和卷部分上有重要效果主要α板条和宽度的方面比率和卷部分和第二等的α板条的卷部分。当样品是与答案处理对待的热时,球状的α阶段首先在LSFed样品被观察(950°C,冷却的8h/air(交流))或与答案处理(950°C,1h/AC)并且老化处理(550°C,在8h/AC上面)分别地。在热处理期间在LSFedTi-6Al-4V合金变粗和α阶段的globularization机制被介绍。为LSFedTi-6Al-4V合金获得好综合机械性质,优化的热处理政体被建议。
简介:做Al的LiVPO4F阴极材料LiAlxV1-xPO4F被反应基于carbothermal减小(CTR)处理的二拍子的圆舞准备。做Al的LiVPO4F的性质被X光检查衍射(XRD)调查,扫描电子显微镜学(SEM),和电气化学的大小。XRD研究证明做Al的LiVPO4F有象undopedLiVPO4F的一样的三斜晶系的结构(空间组p1)。做Al的LiVPO4F的粒子尺寸比undopedLiVPO4F的小并且最小的粒子尺寸仅仅是大约1m的SEM图象展览。做Al的LiVPO4F为第二等的锂电池作为阴极材料被评估,并且展出了改进可逆性和cycleability,它可以被稳定三斜晶系的结构归因于Al3+离子的增加。
简介:Anewenvironmentalfriendlycatalyst,H4SiW12O40/PAnwaspreparedandidentifiedbymeansofFT-IR,XRDandTG/DTA.Cyclohexanone1,2-propanediolketalwassynthesizedfromcyclohexanoneand1,2-propanediolinthepresenceofH4SiW12O40/PAn.Thefactorsinfluencingthesynthesiswerediscussedandthebestconditionswerefoundout.Theoptimumconditionsare:molarratioofcyclohexanoneto1,2-propanediolis1:1.4,thequantityofcatalystisequalto1.0%offeedstocks,andthereactiontimeis40min.H4SiW12O40/PAnisanexcellentcatalystforsynthesizingcyclohexanone1,2-propanediolketalanditsyieldcanreachover96.5%.
简介:Thewell-distributionspindleLiFePO4(LFP)nanoparticlesascathodeoflithiumsecondarybatteriesweresynthesizedbyasolvothermalreactionrouteatlowtemperature(180°C)inwhichtheascorbicacidwasusedasreducingagent.InordertoguaranteethatthepHvaluesofthermalsystemswerenotaffectedtoomuchandthereducibilityofthesystemwasenhancedatthesametime,glucosewaschosenasanauxiliaryreductantinthisreaction.TheobtainedpowderswerecharacterizedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM),andlaserparticleanalyzer.Theresultsshowthatthecarbon-coateduniformspindleolivineLiFePO4/C-glucoseparticles(glucoseasauxiliaryreductant,LFP/C-G)arepreparedwiththesize500–600nmandwithoutanyimpurityphases.Theirelectrochemicalpropertieswereevaluatedbyelectrochemicalimpedancespectroscopy,cyclicvoltammetry,andgalvanostaticcharge/dischargetests.LFP/C-Ghasahigherconductivityandbetterreversiblecapabilitythancarbon-coatedLFP(LFP/C).ThehighestdischargecapacityofLFP/C-Gis161.3mAh·g-1at0.1Cand108.6mAh·g-1at5.0C,respectively.TheresultsimplythattheneatcrystalnanostructureofLFP/C-Ghasexcellentcapacityretentionandcyclingstability.Theaddingofglucoseisthekeyfactorforthewelldistributionandneatcrystalstructureofnanoparticles,thustheelectrochemicalperformancesofmaterialsareimproved.
简介:TheeffectofyttriaonthesolidreactionmechanismofaCaHPO4·2H2O+CaCO3systematdifferenttemperatureswasexperimentallystud-ied.Thesampleswithandwithoutyttriaweresubjectedtothermogravimetric/differentialscanningcalorimetrymeasurement.ThesampleswereheattreatedatthetemperaturescorrespondingtothepeaksontheDSCspectra,andtheresultedphasecompositionswereidentifiedbyX-raydiffraction.Thetransformationmechanismwasdeducedbycomparingthephasesobtainedatdifferenttemperatures.Theresultsshowthatthetransformationsatbelow1073Karenotaffectedbyyttria,butallthoseatabove1073Karecompletelyaltered.Theformationtem-peratureofhydroxyapatitedecreasesby134K,andthedecompositiontemperatureincreasesby38K.ThepolymorphoustransformationofCa3(PO4)2fromβphasetoαphaseincreasesby47K.Thethermodynamicpropertiesofthetransformationsatabove1073Karealsomodi-fiedbytheadditionofyttria;thatis,theendothermalpeaksaresubstitutedbyexothermalpeaks.