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简介：ThecapacitytocaptureCO2wasdeterminedinseveralstoichiometriccompositionsintheLi2O–Bi2O3system.Thecompounds（Li7BiO6,Li5BiO5,Li3BiO4andLiBiO2phases）weresynthesizedviasolid-statereactionandcharacterizedbyX-raydiffraction,scanningelectronmicroscopyandN2adsorptiontechniques.Thesampleswereheat-treatedattemperaturesfrom40to750°CundertheCO2atmospheretoevaluatethecarbonateformation,whichisindicativeofthecapacityofCO2capture.Moreover,Li7BiO6showsanexcellentCO2capturecapacityof7.1mmol/g,whichisconsiderablyhigherthanthoseofotherpreviouslyreportedceramics.Li7BiO6isabletoreactwithCO2from240°Ctoapproximately660°CshowingahighkineticreactionevenatCO2partialpressurevaluesaslowas0.05.

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简介：ThecorrelationbetweenphasestructuresandsurfaceacidityofAl2O3supportscalcinedatdifferenttemperaturesandthecatalyticperformanceofNi/Al2O3catalystsintheproductionofsyntheticnaturalgas(SNG)viaCOmethanationwassystematicallyinvestigated.Aseriesof10wt%NiO/Al2O3catalystswerepreparedbytheconventionalimpregnationmethod,andthephasestructuresandsurfaceacidityofAl2O3supportswereadjustedbycalciningthecommercialγ-Al2O3atdifferenttemperatures(600–1200C).COmethanationreactionwascarriedoutinthetemperaturerangeof300–600Catdifferentweighthourlyspacevelocities(WHSV=30000and120000mL·g-1h-1)andpressures(0.1and3.0MPa).ItwasfoundthathighcalcinationtemperaturenotonlyledtothegrowthinNiparticlesize,butalsoweakenedtheinteractionbetweenNinanoparticlesandAl2O3supportsduetotherapiddecreaseofthespecificsurfaceareaandacidityofAl2O3supports.Interestingly,NicatalystssupportedonAl2O3calcinedat1200C(Ni/Al2O3-1200)exhibitedthebestcatalyticactivityforCOmethanationunderdifferentreactionconditions.LifetimereactiontestsalsoindicatedthatNi/Al2O3-1200wasthemostactiveandstablecatalystcomparedwiththeotherthreecatalysts,whosesupportswerecalcinedatlowertemperatures(600,800and1000C).ThesefindingswouldthereforebehelpfultodevelopNi/Al2O3methanationcatalystforSNGproduction.

简介：A60%Fe/Al2O3catalystwaspreparedbytheco-precipitationmethod.ItwasreducedbyH2toproducemetallicFe,whichwasthensulfidedbyCS2toFe0.96SandFe3S4orphosphidedbytriphenylphosphine(PPh3)inliquidphasestoFe2PandFeP.Itwasfoundthattheironsulfides(Fe0.96SandFe3S4)exhibitedthelowactivityforthehydrodesulfurization(HDS)reactions.TheHDSactivitywasalsolowontheFe(metal)/Al2O3andFe2P/Al2O3catalystssincetheywereconvertedintoFe0.96SandFe3S4duringtheHDSreactions.Incontrast,theFeP/Al2O3wasfoundtobestableandactivefortheHDSreactions.Inparticular,FeP/Al2O3possessedsignificantlysmallerFePparticlesthanFeP/C,leadingtothesignificanthigherHDSactivityofFeP/Al2O3thanFeP/C.

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简介：ThenewKEKCentralcomputersystememployedHPSSfordatamanagementTogainhighperformanceaccesstoHPSSeasily,webuiltawrapperoftheclientAPL.

简介：Pureandneodymium-dopedgadoliniumcalciumoxoboratecrystalsofhighqualityweregrownbytheCzochralskimethod.Theorientationofcrystalwaspreciselydetermined,andthesamplesformeasurementswereprepared.Throughsynchrotronx-raytopographyandhigh-resolutionx-raydiffractometry,thetwinstructurewasdiscovered.Somepropertiessuchasthefigureofmeritvalue,anddielectric,piezoelectric,andelasticconstantsweremeausuredalongwithadiscussionoftheanisotropyofthelaserproperties.

简介：Aseriesofoxygenpermeabledual-phasecompositeoxides60wt%Ce0.8Gd0.2O2-δ-40wt%LnBaCo2O5+δ(CGO-LBCO,Ln=La,Pr,Nd,Sm,GdandY)weresynthesizedthroughasol-gelrouteandeffectsoftheLn3+cationsontheirphasestructure,oxygenpermeabilityandchemicalstabilityagainstCO2wereinvestigatedsystemicallybyXRD,SEM,TG-DSCandoxygenpermeationexperiments.XRDpatternsrevealthatthelargerLn3+cations(La3+,Pr3+andNd3+)successfullystabilizedthedouble-layeredperovskitestructureofsinteredLBCO,whilethesmallerones(Sm3+,Gd3+,andY3+)resultedinthepartialdecompositionofLBCOwithsomeimpuritiesformed.CGO-PBCOyieldsthehighestoxygenpermeationflux,reaching2.8×10-7mols-1cm-2at925?Cwith1mmthicknessunderair/Hegradient.TheTG-DSCprofilesin20mol%CO2/N2andoxygenpermeabilityexperimentswithCO2assweepgasshowthatCGO-YBCOdemonstratesthebestchemicalstabilityagainstCO2,possiblyduetoitsminimumbasicity.ThestableoxygenpermeationfluxofCGO-YBCOunderCO2atmosphererevealsitspotentialapplicationintheoxy-fuelcombustionrouteforCO2capture.

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简介：TomoreindepthunderstandthedopingeffectsofoxygenonSiGealloys,boththemicro-structureandpropertiesofO-dopedSiGe(including:bulk,(001)surface,and(110)surface)arecalculatedbyDFT+Umethodinthepresentwork.Thecalculatedresultsareasfollows.(i)The(110)surfaceisthemainexposingsurfaceofSiGe,inwhichOimpuritypreferstooccupythesurfacevacancysites.(ii)ForOinterstitialdopingonSiGe(110)surface,theexistencesofenergystatescausedbyOdopinginthebandgapnotonlyenhancetheinfraredlightabsorption,butalsoimprovethebehaviorsofphoto-generatedcarriers.(iii)ThefindingaboutdecreasedsurfaceworkfunctionofO-dopedSiGe(110)surfacecanconfirmpreviousexperimentalobservations.(iv)Inallcases,Odoingmainlyinducestheelectronicstructuresnearthebandgaptovary,butisnotdirectlyinvolvedinthesevariations.Therefore,thesefindingsinthepresentworknotonlycanprovidefurtherexplanationandanalysisforthecorrespondingunderlyingmechanismforsomeoftheexperimentalfindingsreportedintheliterature,butalsoconducetothedevelopmentofμc-SiGe-basedsolarcellsinthefuture.

简介：合成了六铝酸盐ＳｒＮｉＡｌ１１Ｏ１９并用ＸＲＤ、ＵＶＤＲＳ、ＴＧＤＴＡ和ＴＥＭ等技术对其进行了表征。在７５０℃于ＳｒＮｉＡｌ１１Ｏ１９上进行的甲烷与二氧化碳重整反应表明，这类催化剂较Ｎｉ／ＳｒＡｌ１２Ｏ１９具有较大活性和低积碳能力，在催化反应过程中可有效地抑制Ｎｉ颗粒的增大。

简介：TheNd2O3nanoparticleswhichmodifiedbyAOTwaspreparedusingmicrioemulsionmethodinthesystemofwater/xylene.L3edgeXAFSwasusedtodeterminethedifferenceofthelocalstructurearundNd^3+ionandtheelectricalstructurebetweenthenanocystallineNd2O3andthecoarsebulkmicrocrystallineNd2O3.ItwasfoundthatNd-Odistanceincreasedwiththeformofnanocrystalliteandtheintensityofabsorptionedgealsoenhancedatthesametime.

简介：Nanostructuredγ-Al2O3withhighsurfaceareaandmesoporousstructurewassynthesizedbysol-gelmethodandemployedascatalystsupportfornickelcatalystsinmethanereformingwithcarbondioxide.ThepreparedsampleswerecharacterizedbyXRD,N2adsorption-desorption,TPR,TPO,TPH,NH3-TPDandSEMtechniques.TheBETanalysisshowedahighsurfaceareaof204m2g-1andanarrowpore-sizedistributioncenteredatadiameterof5.5nmforcatalystsupport.TheBETresultsrevealedthatadditionoflanthanumoxidetoaluminumoxidedecreasedthespecificsurfacearea.Inaddition,TPRresultsshowedthatadditionoflanthanumoxideincreasedthereducibilityofnickelcatalyst.Thecatalyticevaluationresultsshowedanincreaseinmethaneconversionwithincreasinglanthanumoxideto3mol%andfurtherincreaseinlanthanumcontentdecreasedthecatalyticactivity.TPOanalysisrevealedthatthecokedepositiondecreasedwithincreasinglanthanumoxideto3mol%.SEMandTPHanalysesconfirmedtheformationofwhiskertypecarbonoverthespentcatalysts.AdditionofsteamandO2todryreformingfeedincreasedthemethaneconversionandledtocarbonfreeoperationincombinedprocesses.

简介：Aquantumdynamiccalculationonafive-dimensionalO2/LiF（001）modelsystemisperformedusingthemulti-configurationtime-dependentHartreemethod.Theobtainedresultsshowthatthemechanismofrotationalanddiffractiveexcitationindetails:Comparisonwiththerotationalexcitedstate,theinitiallynon-rotationalstateisseentofavortheinelasticscatteringintherotationalexcitationprocess.Thesurfacecorrugationcandampthequantuminterferencesandproduceagreateramountofrotationalinelasticscatteringattheexpenseoftheelasticprocessintherotationalexcitationprocess.Thediffractionprocessandtheaverageenergytransferredintotherotationalanddiffractivemodearealsodiscussed.

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简介：Ｓｔｕｄｙ　ｏｆ　Ｆｕｓｉｏｎ　ｗｉｔｈ　Ｂｉｎａｒｙ　Ｐｒｏｃｅｓｓ　ｉｎ　１６Ｏ＋４５Ｓｃ　ＲｅａｃｔｉｏｎＳｔｕｄｙｏｆＦｕｓｉｏｎｗｉｔｈＢｉｎａｒｙＰｒｏｃｅｓｓｉｎ１６Ｏ＋４５ＳｃＲｅａｃｔｉｏｎ￥ＷａｎｇＳｈｕｆａｎ...

简介：磁铁矿(Fe3有不同尺寸和形状的O4)nanoparticles被热分解方法综合。二条途径，非注射一个壶和热注射的方法，被设计详细调查生长机制。nanoparticles的尺寸和形状被调整先锋集中和持续时间时间决定，这被发现，它能好在我们的合成系统基于LaMer模型由机制解释了。monodisperseFe3O4nanoparticles从5nm有一条吝啬的直径到16nm，和形状进化从对球形三角形、立方。磁性是尺寸依赖者，和Fe3在关于在房间温度和最大的浸透磁化的5nm展览superparamagnetic性质的小尺寸的O4nanoparticles来临到78emu/g，而Fe3O4nanoparticles当直径增加到大约16nm时，开发铁磁性的性质。

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简介：Weinvestigatetheareadistributionofclusters(loops)inthehoneycombO(n)loopmodelbymeansofthewormalgorithmwithn=0.5,1,1.5,and2.Atthecriticalpoint,thenumberofclusters,whoseenclosedareaisgreaterthanA,isproportionaltoA-1withaproportionalityconstantC.WeconfirmnumericallythatCisuniversal,anditsvalueagreeswellwiththepredictionsbasedontheCoulombgasmethod.