简介:ThemixturemodelofAl85Y4Nd4Ni7alloyinwhichapartiallycrystallizedamorphousalloyisregardedasananocompositeofanAlnanoparticleandaremainingamorphousmatrixispresented.Itsevolutionintheprocessofcrystallizationhasbeeninvestigatedbydifferentialscanningcalorimetry(DSC),X-raydiffraction(XRD),andtransmissionelectronmicroscopy(TEM).Mainlyamorphousstructurewithα-Alnanocrystalsembeddedintheamorphousmatrixhasbeenrevealedbymeltspiningthealloy.Crystallizationisshowedtooccurinthreestages:(1)crystallizationofamorphousalloyandformationofAlNiY,AlNdNiandunknowncrystallinephases,(2)formationofAl3YandAl3Nd,and(3)formationofAl3Ni.
简介:ToinvestigatethedegradationofcorrosionresistanceofZircaloy-4inLiOHaqueoussolution,SIMS(secondaryionmassspectrometry)analysiswasperformedtoexaminetheprofilesofLi+,K+,andOH-inoxidelayersformedinthesameconcentration(0.1mol/L)LiOHandKOHsolutions.Eventhoughtheoxidelayershaveanequalthickness,thepenetrationdepthofK+isshallowerthanthatofLi+,andthepenetrationdepthofOH-corrodedinKOHsolutionisalsoshallowerthanthatcorrodedinLiOHsolution.ItshowsthatthediffusionofOH-intooxidelayerisaccompaniedbythecorrespondingcation.ThedifferenceofdegradationeffectofLiOHandKOHsolutionsonthecorrosionresistanceofZircaloy-4wasdiscussed.
简介:Dynamicsinpartialtransientliquidphasebonding(PTLPbonding)ofSi3N4ceramicwithTi/Cu/Timulti-interlayerwassystematicallystudiedthroughmicro-analysisofjointinterfaces.Theresultsshowthatgrowthofreactionlayerandisothermalsolidificationprocessiondoatthesametime.GrowthofreactionlayerandmovingofisothermalsolidificationinterfaceobeytheparaboliclawgovernedbythediffusionofparticipatingelementsduringthePTLPbonding.Coordinationoftheabovetwodynamicsprocessisdonethroughtimeandtemperature.Whenreactionlayerthicknessissuitableandisothermalsolidificationprocessisfinished,thehighbondingstrengthatroomtemperatureandhightemperatureareobtained.
简介:SphericalLiFePO4andLiFePO4/Ccompositepowdersforlithiumionbatteriesweresynthesizedbyanovelprocessingrouteofco-precipitationandsubsequentcalcinationsinanitrogenandhydrogenatmosphere.TheprecursorsofLiFePO4,LiFePO4/CcompositeandtheresultantproductswerecharacterizedbyX-raydiffraction(XRD),scanningelectronmicroscope(SEM),andtheelectrochemicalperformanceswereinvestigatedbygalvanostaticchargeanddischargetests.TheprecursorscomposedofamorphousFe3(PO4)2·xH2OandcrystallineLi3PO4obtainedintheco-precipitationprocessinghaveasphere-likemorphology.ThesphericalLiFePO4derivedfromthecalcinationsoftheprecursorat700℃for10hinareductionatmosphereshowsadischargecapacityof119mAh·g-1attheC/10rate,whiletheLiFePO4/Ccompositewith10wt.%carbonadditionexhibitsadischargecapacityof140mAh·g-1.TheelectrochemicalperformancesindicatethattheLiFePO4/CcompositehasahigherspecificcapacityandamorestablecyclingperformancethanthebareolivineLiFePO4duetothecarbonadditionenhancingtheelectronicconductivity.
简介:ElectrocrystallizationMechanismofTungsteninMoltenKF-B_2O_3-K_2WO_4WenZhenhuanandLiGuoxun文振环,李国勋(GeneralResearchInstiiuteforNo...
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: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:本文介绍Si3N4(代替部分金刚石浓度)配合铁基(以Fe代Co)结合剂氮化金刚石薄膜涂层节块,可大大降低成本,该节块性能良好,有较高使用效果及经济效益。
简介:ThelongafterglowSrAl2O4:Dy,Euphosphorisliabletohydrolyzeinwaterwithdeteriorationoftheluminescentproperty.SrAl2O4:Dy,Euphosphorswerethereforeheatedat60-90℃inTEOSsoltoformasurfacegelandthenheat-treatedat400℃toobtainSiO2coatedphosphors.ObservationbyTransmissionElectronMicroscope(TEM)andX-rayphotoelectronspectroscopy(XPS)showsthatathinsilicafilmformsonthesurfaceofthephosphors.Thecoatingprocedurecanbeillustratedbyafour-stepprocessandthetransparentsilicafilmcansuppressthehydrolysisprocess,sothattheluminescentpropertiesofthephosphorsareunimpairedorevenbetter.
简介:1IntroductionTherareearthcobaltalloyshavethepotentialformakingthemagneticandmagnetoopticalmaterials.Sofar,therareearthcobaltalloyfilmsaresubstantiallyproducedbysputteringorvacuumplating.Ifsuchfilmsarepreparedbyelectrodepositioninstead,productionefficiencywouldbeimprovedandthecompositionofthealloycouldbecontrolled.Becausetheoxidationreductionpotentialsofrareearthelementsareverynegative,organicsolventsmaybeusedaselectrolyticmedia.ElectrodepositionofGdCoandSmCoinorganicsolutionshasbeenreporte...