简介：［1］A.G.Khachaturyan,T.F.Lindsey,J.W.Morris,Jr:Metall.Trans.,19(1988),p.249.［2］V.Radmilovic,A.G.Fox,G.Thomas:ActaMetall.,37(1989),p.2385.［3］B.J.Shaiu,H.T.Li,HaydnChen:Metal.Trans.,21(1990),p.1133.［4］G.Schmitz,P.Haasen:ActaMetall.Mater.,40(1992),p.2209.［5］V.Mahadev,K.Mahalingam,G.L.Liedl,etal.:ActaMetall.Mater.,42(1994),p.1039.［6］P.Haasen:PhaseTransformationsinMaterials.VCH,Weinheim,1991.［7］L.Q.Chen,A.G.Khachaturyan:ActaMetall.Mater.,39(1991),p.2533.［8］L.Q.Chen,A.G.Khachaturyan:ScriptaMetall.,25(1991),p.67.［9］R.Poduri,L.Q.Chen:ActaMetall.Mater.,44(1996),p.4253.［10］A.Chakrabarti:Phys.Rev.,45(1992),p.9620.［11］H.Tanaka,TakeshiYokokawa,HajimeAbe,etal.:Phys.Rev.Lett.,65(1990),p.3136.
简介：ＥｌｅｃｔｒｏｃｒｙｓｔａｌｌｉｚａｔｉｏｎＭｅｃｈａｎｉｓｍｏｆＴｕｎｇｓｔｅｎｉｎＭｏｌｔｅｎＫＦ－Ｂ＿２Ｏ＿３－Ｋ＿２ＷＯ＿４ＷｅｎＺｈｅｎｈｕａｎａｎｄＬｉＧｕｏｘｕｎ文振环，李国勋（ＧｅｎｅｒａｌＲｅｓｅａｒｃｈＩｎｓｔｉｉｕｔｅｆｏｒＮｏ...
简介：LayeredcathodematerialLiCo1/3Ni1/3Mn1/3O2wassynthesizedbyPechiniprocess,andinvestigatedusingX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andgalvanostaticcharge/dischargecycling.Thesampleiswell-crystallizedandhasaphase-purea-NaFeO2structure.Theparticlesizesareuniform,anddistributedintherangeof20-200nm.TheinitialdischargecapacityoftheLi/LiCo1/3Ni1/3Mn1/3O2cellwasabout149mAh·g-1whenitwascycledatavoltagerangeof4.5-2.3Vwithaspecificcurrentof0.25mA.Theresultisbetterincomparisonwithsolid-statesolutionmethod.Thesyntheticprocedurewasdiscussed.Threemajorreactions:chelation,esterification,andpolymerizationsuccessivelyoccurred.
简介：Thecorrosionbehaviorandanti-corrosionmechanismoftheZn-Ni-Al2O3compositecoatingwereinvestigatedbySEM,EDSandXPS.TheresultsindicatethatthecorrosiontypeoftheZn-Ni-Al2O3coatingsinneutral5wt.%NaClsolutionisuniformcorrosion.ThepresenceofcompactanduniformlydispersednanoaluminaparticlessubstantiallyinhibitsthecorrosionofZn-Ni-Al2O3compositecoatings.Intheinitialcorrosionstage,thecorrosiveproductsofZn-NimatrixformacompactZnCl2·4Zn(OH)2layer.Withthedevelopmentofcorrosion,somenanoaluminaparticlesareembeddedandformaNienrichmentlayer.InNienrichmentlayer,NipresentsasNiandNiO.
简介：ＳｃａｎｎｉｎｇＥｌｅｃｔｒｏｎＭｉｃｒｏｓｃｏｐｙＳｔｕｄｉｅｓｏｆＹＢａ＿２Ｃｕ＿３Ｏ＿（７－δ）ＳｕｐｅｒｃｏｎｄｕｃｔｏｒｓＳｈａＷｅｉ（沙维）（ＤｅｐａｒｔｍｅｎｔｏｆＣｉｖｉｌＥｎｇｉｎｅｅｒｉｎｇ，ＴｈｅＱｕｅｅｎ′ｓＵｎｉｖｅｒｓｉｔ...
简介：EmployingLi2CO3,NiO,Co3O4,andMnCO3powdersasstartingmaterials,Li[Ni1/3Co1/3Mn1/3]O2wassynthesizedbysolid-statereactionmethod.Variousgrindingaidswereappliedduringmillinginordertooptimizethesynthesisprocess.Aftersuccessiveheattreatmentsat650and950℃,thepreparedpowderswerecharacterizedbyX-raydiffraction(XRD)analysis,scanningelectronmicroscopy,andtransmissionelectronmicroscopy.Thepowderspreparedbyaddingsalt(NaCl)asgrindingaidexhibitaclearR3mlayerstructure.ThepowdersbyothergrindingaidslikeheptaneshowsomeimpuritypeaksintheXRDpattern.Theformerpowdersshowauniformparticlesizedistributionoflessthan1μmaveragesizewhilethelattershowsawidedistributionrangingfrom1to10μm.EnergydispersiveX-ray(EDX)analysissshowthattheratioofNi,Co,andMncontentinthepowderisapproximately1/3,1/3,and1/3,respecively.TheEDXdataindicatenoincorporationofsodiumorchlorineintothepowders.Charge-dischargetestsgaveaninitialdischargecapacityof160mAh·g-1forthepowderswithNaCladditionwhile70mAh·g-1forthepowderswithheptane.
简介：TherelationshipofelectricalpropertiesofMn-dopedBa0.92Ca0.08TiO3PTCR(positivetemperaturecoefficientresistance)ceramicswithtwosinteringscheduleswasdiscussed.UsingTEM(transmissionelectronmicroscope)combinedwithEDS(energydispersiveX-rayspectrometer),theMnionsdistributedatgrainboundarieswereanalyzed.TheresultsshowthatthePTCReffectofMn-dopedPTCRceramicsismoredependentonthesinteringschedulethanthoseofMnfree.ThephenomenonmaybecausedbythevalencestatesvarianceofMnionssegregatedatthegrainboundaries.
简介：AnewtypeofcomplexsolidsuperacidcatalystWO3-ZrO2-SO42-withanacidstrengthH0≤-16.04waspreparedbykneadingZr（OH）4oramorphousZrO2withtungsticacid（H2WO4）（W/Zr=0.15）,followedbyexposingthiscomplexhydroxidesto0.5tool/LH2SO4,calcininginairat700～800℃for3h.ThiscatalystpossessesbothstrongBronstedacidityandstrongLewisacidityexperimentallyshowedbyIRobservationofpyridineabsorbedonit.XPSandAEStechniqueswereemployedtoexaminethevalencestatesoftungsten,zirconium,sulfurandtheirinteractions.Thestructureofsulfurspecieswasstudiedbyinfraredspectroscopyandastructuremodelofactivesitewasproposedupontheseresults.
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：1ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅｒａｒｅｅａｒｔｈｃｏｂａｌｔａｌｌｏｙｓｈａｖｅｔｈｅｐｏｔｅｎｔｉａｌｆｏｒｍａｋｉｎｇｔｈｅｍａｇｎｅｔｉｃａｎｄｍａｇｎｅｔｏｏｐｔｉｃａｌｍａｔｅｒｉａｌｓ.Ｓｏｆａｒ,ｔｈｅｒａｒｅｅａｒｔｈｃｏｂａｌｔａｌｌｏｙｆｉｌｍｓａｒｅｓｕｂｓｔａｎｔｉａｌｌｙｐｒｏｄｕｃｅｄｂｙｓｐｕｔｔｅｒｉｎｇｏｒｖａｃｕｕｍｐｌａｔｉｎｇ.Ｉｆｓｕｃｈｆｉｌｍｓａｒｅｐｒｅｐａｒｅｄｂｙｅｌｅｃｔｒｏｄｅｐｏｓｉｔｉｏｎｉｎｓｔｅａｄ,ｐｒｏｄｕｃｔｉｏｎｅｆｆｉｃｉｅｎｃｙｗｏｕｌｄｂｅｉｍｐｒｏｖｅｄａｎｄｔｈｅｃｏｍｐｏｓｉｔｉｏｎｏｆｔｈｅａｌｌｏｙｃｏｕｌｄｂｅｃｏｎｔｒｏｌｌｅｄ.Ｂｅｃａｕｓｅｔｈｅｏｘｉｄａｔｉｏｎｒｅｄｕｃｔｉｏｎｐｏｔｅｎｔｉａｌｓｏｆｒａｒｅｅａｒｔｈｅｌｅｍｅｎｔｓａｒｅｖｅｒｙｎｅｇａｔｉｖｅ,ｏｒｇａｎｉｃｓｏｌｖｅｎｔｓｍａｙｂｅｕｓｅｄａｓｅｌｅｃｔｒｏｌｙｔｉｃｍｅｄｉａ.ＥｌｅｃｔｒｏｄｅｐｏｓｉｔｉｏｎｏｆＧｄＣｏａｎｄＳｍＣｏｉｎｏｒｇａｎｉｃｓｏｌｕｔｉｏｎｓｈａｓｂｅｅｎｒｅｐｏｒｔｅ...
简介：LaCrO_3的nano粉末被一条大音阶的第五音胶化线路准备。从350～550K的LaCrO_3nano粉末的热能力被DSC方法测量并且是表示了:C_(p(LaCrO3))(±0.112)=166.844-8.500x10~(-3)T-1.022x10~6T~(-2)(J/(摩尔·K))(350-550K)。一个EMF测量集会为流电的房间作为电解质与CaF_2被开发。可逆房间的FrommeasuredEMF数据，(-)磅，La_2O_3，LaF_3，|CaF_2|O_2(1atm)，LaF_3，LaCrO_3，Cr_2O_3，磅(+)，和吉布斯的相关价值释放的O_2(1atm)精力，吉布斯LaCrO_3的形成的免费精力从700～885K被计算：ΔG_(f，LaCrO3)~Θ=-1555.364+0.354T(kJ/mol)(700-885K)。并且免费精力从简单氧化物La_2O_3andCr_2O_3反应改变的吉布斯是打算的是：ΔG_(f，公牛(LaCrO3))~Θ=-94.758+8.530x10~(-2)T(kJ/mol)(700-885K)。
简介：TiO2nanoparticleswithdifferentphasesarepreparedbyhydrolysisoftitaniumtetrabutoxideinthepresenceofHCl.ThecompositionandmicrostructureoftheresultingsamplesarestudiedbyXRDandTEM.TheseresultsshowthattherangeofparticlesizeofTiO2isfrom20to30nm.ThemechanismofTiO2photocatalysisreactionhasbeendiscussedextensively.PhotocatalyticactivitiesofnanometerTiO2arealsoevaluatedbydegradationofthecrystalvioletsolution.ExperimentalresultsindicatethatthesynergisticactionofH2O2andultrasonicwavegreatlyenhancesphoto-catalyticreactionofTiO2.
简介：［1］S.Jin,T.H.Tiefel,M.McCormack,etal.:Sci-ence,264(1994),p.413.［2］R.vonHelmolt,J.Wecker,B.Holzapfel,etal.:Phys.Rev.Lett.,71(1993),p.2331.［3］Y.Shimakawa,Y.Kubo,T.Manako:Nature,379(1996),p.53.［4］C.Zener:Phys.Rev.,82(1951),p.403.［5］A.J.Millis,P.B.Littlewood,B.I.Shraiman:Phys.Rev.Lett.,74(1995),p.5144.［6］A.J.Millis,B.I.Shraiman,R.Mueller:Phys.Rev.Lett.,77(1996),p.175.［7］D.Louca,T.Egami,E.L.Brosha,:Phys.Rev.B,56(1997),p.8475.［8］G.Zhao,K.Conder,H.Keller,etal.:Nuture,381(1996),p.676.［9］C.H.Booth,F.Bridges,G.J.Snyder,etal:Phys.Rev.B,54(1996),p.15606.［10］K.H.Kim,J.Y.Gu,H.S.Choi,etal.:Phys.Rev.Lett.,77(1996),p.1877.［11］S.Zhou,G.Zhou,Y.Zhang:Jpn.J.Appl.Phys.,38(1999),p.5075.［12］S.Tajima,A.Masaki,S.Uchida,etal.:J.Phy.C:SolidStatePhys.,20(1987),p.3469.［13］L.M.Rodriguez-Martinez,J.P.Attfield:Phys.Rev.B,58(1998),p.2426.
简介：本文采用磁粉、X射线、CT和超声等无损检测和金相分析等方法对40CrNi2Si2,MoVA钢制零件的磁痕显示进行了系统分析。研究认为，40CrNi2Si2MoVA钢制零件的磁痕显示为显微成分沿变形方向偏析导致的马氏体转变点Ms差异所致。显微成分偏析是钢锭结晶过程中不可避免的，但可通过优化熔炼工艺参数降低显微偏析的程度。本文还分析了四种磁痕显示的类型及其判别方法。
简介：ItiswellknownthatthephotocatalyticactivityofTiO2thinfilmsstronglydependsonthepreparingmethodsandpost-treatmentconditions,sincetheyhaveadecisiveinfluenceonthechemicalandphysicalpropertiesofTiO2thinfilms.Therefore,itisnecessarytoelucidatetheinfluenceofthepreparationprocessandpost-treatmentconditionsonthephotocatalyticactivityandsurfacemicrostructuresofthefilms.ThisreviewdealswiththepreparationofTiO2thinfilmphotocatalystsbywet-chemicalmethods(suchassol-gel,reversemicellarandliquidphasedeposition)andthecomparisonofvariouspreparationmethodsaswellastheiradvantageanddisadvantage.Furthermore,itisdiscussedthattheadvancementofphotocatalyticactivity,super-hydrophilicityandbactericidalactivityofTiO2thinfilmphotocatalystinrecentyears.
简介：Thesegregationanddiffusionofboronduringheattreatmentswerestudied.Theinfluenceofboroncontents,agingtimeandappliedstressonFeMo2B2formationwasalsostudied.Finally,theeffectsofboroncontentsandFeMo2B2formationonthehightemperaturestrengthwerestudied.Boronatomsweresegregatedtoprioraustenitegrainboundaryduringnormalizingtreatment.Andtheseboronatomswereslowlydiffusedintothegraininteriorduringtemperingandagingat700℃.TheFeMo2B2phasewasonlyformedafter1,000hagingat700℃inalloycontaining196ppmboron.TheformationofFeMo2B2phaseisacceleratedbytheappliedstress.ItwasexpectedthattheformationofFeMo2B2iscloselyrelatedtotheredistributionofboronatoms.Thetensilestrengthsat700℃areincreasedwiththeincreaseofboroncontents.However,theformationofFeMo2B2phaseresultsinlowertensilestrength.
简介：Byuseofmicro-DTAtechniqueaswellasambientandhightemperatureX-rayanalysisthephasediagramofNaCl-CaCl2hasbeenchecked.Itis.asimpleeutecticsystemwithasolidsolubilityinthesodiumchlorideside.Theeutecticpointisat773K,49mol%NaCl.Theexperimentalresults,especiallythoseoftheX-raydiffractionstudieshaveshowedthattheincongruentcompound4NaCl-CaCl2doesnotexistintheNaCl-CaCl2system.
简介：ThelongafterglowSrAl2O4:Dy,Euphosphorisliabletohydrolyzeinwaterwithdeteriorationoftheluminescentproperty.SrAl2O4:Dy,Euphosphorswerethereforeheatedat60-90℃inTEOSsoltoformasurfacegelandthenheat-treatedat400℃toobtainSiO2coatedphosphors.ObservationbyTransmissionElectronMicroscope(TEM)andX-rayphotoelectronspectroscopy(XPS)showsthatathinsilicafilmformsonthesurfaceofthephosphors.Thecoatingprocedurecanbeillustratedbyafour-stepprocessandthetransparentsilicafilmcansuppressthehydrolysisprocess,sothattheluminescentpropertiesofthephosphorsareunimpairedorevenbetter.
客服QQ：30444492琼网文【2021】1550-113号
增值电信业务经营许可证：琼B2-20210322
出版物经营许可证：新出发龙华出字第(2021)009号
广播电视节目制作经营许可证：(琼)字第00779号
版权所有 ©2002-2024 期刊网(www.qikanchina.com) 琼ICP备2021005105号
![Preparation of Li[Ni1/<b style='color:red'>3</b>Co1/<b style='color:red'>3</b>Mn1/<b style='color:red'>3</b>]O<b style='color:red'>2</b> powders for cathode material in secondary battery by solid-state method](/image/thesis6 "Preparation of Li[Ni1/<b style='color:red'>3</b>Co1/<b style='color:red'>3</b>Mn1/<b style='color:red'>3</b>]O<b style='color:red'>2</b> powders for cathode material in secondary battery by solid-state method")
