简介：采用热处理和机械混合的方法制备CNTs-TiO2锂离子电池负极材料。CNTs-TiO2负极材料的表面形态及物相通过扫描电子显微镜（SEM）、BET比表面积测试和X射线衍射（XRD）仪进行表征;通过充放电循环测试,表征CNTs-TiO2负极材料的充放电库仑效率、充放电性能及循环性能。实验结果表明：CNTs-TiO2在倍率为0.1C时,首次放电比容量达到213mAh·g-1,在第50次循环后,比容量稳定在143mAh·g-1,体现出良好的循环稳定性。

简介：PalladiumcatalystsaresupportedonTiO2,ZrO2,Al2O3,Zr0.5Al0.5O1.75andTiO2-Zr0.5Al0.5O1.75preparedbyco-precipitationmethod,respectively.CatalyticactivitiesformethaneandCOoxidationareevaluatedinagasmixturethatsimulatedtheexhaustfromlean-burnnaturalgasvehicles(NGVs).Pd/TiO2-Zr0.5Al0.5O1.75performsthebestcatalyticactivityamongthetestedfivecatalysts.ForCH4,thelight-offtemperature(T50)is254℃,andthecompleteconversiontemperature(T90)is280℃;forCO,T50is84℃,andT90was96℃.Varioustechniques,includingN2adsorption-desorption,X-raydiffraction(XRD),H2-temperature-programmedreduction(H2-TPR),X-rayphotoelectronspectroscopy(XPS),andscanningelectronmicroscopy(SEM)areemployedtocharacterizetheeffectofsupportsonthephysicochemicalpropertiesofpreparedcatalysts.N2adsorption-desorptionandSEMshowthatTiO2-Zr0.5Al0.5O1.75expressesuniformnano-particlesandlargemeso-porediametersof26nm.H2-TPRandXRDindicatethatPdOiswelldispersedonthesupportsandstronglyinteractedwitheachother.TheresultsofXPSshowthattheelectrondensityaroundPdOandtheproportionofactiveoxygenonTiO2-Zr0.5Al0.5O1.75aremaximaamongthefivesupports.

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简介：InthispaperweusedMOF-5andCu3(BTC)2toseparateCO2/CH4andCH4/N2mixturesunderdynamicconditions.Bothmaterialsweresynthesizedandpelletized,thusallowingforameaningfulcharacterizationinviewofprocessscale-up.ThematerialswerecharacterizedbyX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM).Byperformingbreakthroughexperiments,wefoundthatCu3(BTC)2separatedCO2/CH4slightlybetterthanMOF-5.BecausethecrystalstructureofCu3(BTC)2includesunsaturatedaccessiblemetalsitesformedviadehydration,itpredominantlyinteractedwithCO2moleculesandmoreeasilycapturedthem.Conversely,MOF-5withasuitableporesizeseparatedCH4/N2moreefficientlyinourbreakthroughtest.

简介：ThreeseriesofCeO2/CuOsampleswerepreparedbyimpregnationmethodandcharacterizedbyXRD,N2adsorption-desorption,temperatureprogrammedreduction(TPR),XPSandTEMtechniques.IncomparisonwiththesamplespreparedwithCuOasinitialsupport,thesampleswithCu(OH)2asinitialsupporthavehigherreducibilitiesandsmallerrelativeTPRpeakareas,andalsolargerspecificsurfaceareasatcalcinationtemperaturesof400℃–600℃.Asaresult,Cu(OH)2isbetterthanCuOasinitialsupportforpreferentialoxidationofCOinexcessH2(CO-PROX).Thebestcatalyticperformancewasachievedonthesamplecalcinedat600℃andwithanatomicratioofCe/Cuat40%.XPSanalysesindicatethatmoreinterfacelinkagesCe-O-Cucouldbeformedwhenitwascalcinedat600℃.AndtheatomicratioofCe/Cuat40%ledtoaproperreducibilityforthesampleasillustratedbytheTPRmeasurements.

简介：QuantumdynamicscalculationsforthetitlereactionH(2S)+S2(X3-Σg)→SH(X2Π)+S(3P)areperformedbyusingagloballyaccuratedoublemany-bodyexpansionpotentialenergysurface[J.Phys.Chem.A1155274(2011)].TheChebyshevrealwavepacketpropagationmethodisemployedtoobtainthedynamicalinformation,suchasreactionprobability,initialstate-specifiedintegralcrosssection,andthermalrateconstant.Itisfoundnotonlythatthereisareactionthresholdnear0.7eVinbothreactionprobabilitiesandintegralcrosssectioncurves,butalsothatboththeprobabilityandcrosssectionincreasefirstlyandthendecreaseasthecollisionenergyincreases.Theexistenceoftheresonancestructureinboththeprobabilityandcrosssectioncurvesisascribedtothedeeppotentialwell.Thecalculationoftherateconstantrevealsthatthereactionoccurringonthepotentialenergysurfaceoftheground-stateHS2isslowtotakeplace.

简介：AnewSnO_2-Fe_2O_3/SWCNTs(single-walledcarbonnanotubes)ternarynanocompositewasfirstsynthesizedbyafacilehydrothermalapproach.SnO_2andFe_2O_3nanoparticles(NPs)werehomogeneouslylocatedonthesurfaceofSWCNTs,asconfirmedbyX-raydiffraction(XRD),transmissionelectronmicroscope(TEM)andenergydispersiveX-rayspectroscopy(EDX).Duetothesynergisticeffectofdifferentcomponents,theassynthesizedSnO_2-Fe_2O_3/SWCNTscompositeasananodematerialforlithium-ionbatteriesexhibitedexcellentelectrochemicalperformancewithahighcapacityof692mAh·g~(-1)whichcouldbemaintainedafter50cyclesat200mA·g~(-1).Evenatahighrateof2000mA·g~(-1),thecapacitywasstillremainedat656mAh·g~(-1).

简介：Thereisagrowingsupportforthelowlyingscalarmesonsf0(500),f0(980),a0(980),and(800)tobegenerateddynamicallyfromtheinteractionofpseudoscalarmesons,whilethecaseofthenextsetofscalarresonancesathigherenergies,f0(1370),f0(1710),K0(1430)ismoreaquestionofdebate.Soisthecaseofthetensorresonancesf2(1270),f′2(1525),K2(1430).AnewperspectiveonthesestateshasbeenofferedinRef.[1]wherethef0(1370)andf2(1270)resonancesareshowntobegeneratedfromtheinteractionprovidedbythelocalhiddengaugeLagrangiansimplementingunitarization.Itisshownthattheideaofthenatureofthesestatesasvectormeson-vectormesoncompositestateshasbeentestedinmanyreactions.Yet,thepermanentdiscussionoftheissuedemandsextrachecksforotherobservablesand,inthissense,theweakdecaysbringanewsourceofvaluableinformationthatshouldservetotestdifferentmodels.

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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：Nucleon-nucleon(NN)correlationsandtheirisospindependenceinasymmetricnuclearmatterareofgreatnterestsincetheyarecloselyrelatedtothestructureofneutron-richnuclei[1],particleproductioninheavy-ionollisions[2],andneutron-starphysics[3].Themany-bodycorrelationsamongnucleonscanbedirectlyreflectedintheneutronandprotonspectralfunctions[4],andthelattermayplayanimportantroleinunderstandingthenatureftheNNcorrelations,especiallytheshort-rangeandtensorcorrelationsinasymmetricnuclearmatter.

简介：Inthisstudy,apoly(etherblockamide)(Pebax1657)compositemembraneappliedforCO2capturewaspreparedbycoatingPebax1657solutiononpolyacrylonitrile(PAN)ultrafiltrationmembrane.Ethanol/watermixturewasusedasthesolventofPebaxandtheeffectsofethanol/watermassratiosandPebaxconcentrationonthepermeationpropertiesofcompositemembranewerestudied.Toenhancethecompositemembranepermeance,thegutterlayer,madefromreactiveaminosiliconecrosslinkingwithpolydimethylsiloxane(PDMS),wasdesigned.Theinfluenceofcrosslinkingdegreeofthegutterlayeronmembraneperformancewasinvestigated.Asaresult,aPebax/aminoPDMS/PANmultilayermembranewithhexaneresistancewasdeveloped,showingCO2permeanceof350GPUandCO2/N2selectivityover50.Theblendofpolyethyleneglycoldimethylether(PEG-DME)withPebaxascoatingmaterialwasstudiedtofurtherimprovethemembraneperformance.AfterbeingcombinedwithPEG-DMEadditive,CO2permeanceofthefinalPebax-PEG-DME/amino-PDMS/PANcompositemembranereached400GPUabovewithCO2/N2selectivityover65.

简介：Weprovideanewclassofinteriorsolutionofa(2+1)-dimensionalanisotropicstarinFinchandSkeaspacetimecorrespondingtotheBTZblackhole.WedevelopthemodelbyconsideringtheMITbagmodelEOSandaparticularansatzforthemetricfunctiongrrproposedbyFinchandSkea[M.R.FinchandJ.E.F.Skea,Class.Quantum.Grav.6(1989)467].Ourmodelisfreefromcentralsingularityandsatisfiesallthephysicalrequirementsfortheacceptabilityofthemodel.

简介：MoleculardynamicssimulationsareperformedtostudythegrowthmechanismofCH4-CO2mixedhydrateinxCO2=75%,xCO2=50%,andxCO2=25%systemsatT=250K,255Kand260K,respectively.OursimulationresultsshowthatthegrowthrateofCH4-CO2mixedhydrateincreasesastheCO2concentrationintheinitialsolutionphaseincreasesandthetemperaturedecreases.Viahydrateformation,thecompositionofCO2inhydratephaseishigherthanthatininitialsolutionphaseandtheencagingcapacityofCO2inhydratesincreaseswiththedecreaseintemperature.ByanalysisofthecageoccupancyratioofCH4moleculesandCO2moleculesinlargecagestosmallcages,wefindthatCO2moleculesarepreferablyencagedintothelargecagesofthehydratecrystalascomparedwithCH4molecules.Interestingly,CH4moleculesandCO2moleculesfrequentlyreplacewitheachotherinsomeparticularcagesitesadjacenttohydrate/solutioninterfaceduringthecrystalgrowthprocess.Thesetwospeciesofguestmoleculeseventuallyacttostabilizethenewlyformedhydrates,withCO2moleculesoccupyinglargecagesandCH4moleculesoccupyingsmallcagesinhydrate.

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简介：Wereportedabifunctionalmaterial,Cr-salenimplantedconjugatedmicroporouspolymer(Cr-CMP),whichisabletocaptureexcellentCO2amountsandhasaremarkablecatalyticactivitytowardsthecycloadditionreactionofCO2toepoxidesformingcycliccarbonatesatmildconditionswithoutadditionalsolvents.ThisheterogeneousCr-CMPcatalysthasasuperiorcatalyticactivitytoitsrelatedhomogeneouscatalystandcanbereusedmorethantentimeswithoutasignificantdecreaseincatalyticactivity.