简介:Anenvironmentallyfriendlyprecursor,adenosine,hasbeenusedasadualsourceofCandNtosynthesizenitrogen-dopedcarboncatalystwith/withoutFe.Ahydrothermalcarbonizationmethodhasbeenusedandwateristhecarbonizationmedia.Themorphologyofsampleswith/withoutFecomponenthasbeencomparedbyHRTEM,andtheresultshowsthatFecanpromotethegraphitizationofcarbon.Furtherelectro-chemicaltestshowsthattheoxygenreductionreaction(ORR)catalyticactivityofFe-containingsample(C–FeN)ismuchhigherthanthatoftheFe-freesample(C–N).Additionally,theintermediatesofC–FeNformedduringeachsyntheticprocedurehavebeenthoroughlycharacterizedbymultiplemethods,andthefunctionofeachprocedurehasbeendiscussed.TheC–FeNsampleexhibitshighelectro-catalyticstabilityandsuperiorelectro-catalyticactivitytowardORRinalkalinemedia,withitshalf-wavepotential20mVlowerthanthatofcommercialPt/C(40wt%).Itisfurtherincorporatedintoalkalinepolymerelectrolytefuelcell(APEFC)asthecathodematerialandledtoapowerdensityof100mW/cm~2.
简介:TheeffectofTi(C,N)onpropertiesoflow-carbonMgO-Cbrickswasinvestigated.Thephasecompositionandthemicrostructureofthematrixoflow-carbonMgO-CbrickcontainingTi(C,N)werestudiedbyXRDandSEManalysistogetherwithEDS.TheresultsshowedthatTi(C,N)distributedinthematrixoflow-carbonMgO-Cbrickuniformlyafterbeingtreatedat1600℃for3hincokepowderbed,andTi(C,N)andMgOformedasolidsolution.Afterthetreatmentat1600℃for3hincokepowderbed,thebulkdensityandcoldcrushingstrengthoflow-carbonMgO-CbrickwithTi(C,N)decreased,andtheapparentporosityandlinearchangerateofspecimensincreased.Theoxidationresistanceoflow-carbonMgO-CbrickwithTi(C,N)wassuperiortothatoflow-carbonMgO-Cbrickwithnoadditives,butinferiortothatoflow-carbonMgO-CbrickwithAlpowder.TheslagresistanceofthespecimenwithTi(C,N)wasexcellentaswell.
简介:ThepaperdefinesanextendedCesàrooperatorTgwithholomorphicsymbolgintheunitballBofCnasWhereg(z)=∑j=1∑nzjg/zjistheradialderivativeofg.Inthispaper,theauthorcharacterizesgforwhichTgisbounded(orcompact)ontheBlochspaceBandthelittleBlochspaceB0.
简介:QUALITATIVESTUDYOFSIALOMUCINSCHANGESDURINGN-METHYL-N-NITROSOUREA-INDUCEDCOLONICCARCINOGENESISINMICEWangQiang王强;WangYuanhe王元和;...
简介:ThesubmicronpowdermixturesofTiC-TiN-WC-Mo-C-Nisinteredat1400℃orbelowinvacuumwerestudiedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andtransmissionelectronmicroscopy(TEM)analyses.TheresultsshowedthatMo2Cformedat800℃orbelow.BothWCandMo2Cdisappearedat1200℃,andTiNdisappearedat1250℃.Inaddition,thevariationsoflatticeconstantsofthetitaniumcarbonitrideandnickelbinderphasewithsinteringtemperaturewereexperimentallyobtained,andthereasonwasanalyzed.
简介:Thec-JunN-terminalkinases(JNKs)areclassicstress-activatedproteinkinases.ManycellularstresseshavebeenshowntostimulateJNKactivation.Inthisreview,wefocusonribotoxicstressesbasedontheirmultiplebiologicalpotenciesincludinganti-HIV-1activity.Someofthefunctionsofribotoxinsandthesignalingtransductionpathwaythatmediatedarementioned.Differentfromotherstimulators,ribotoxicstressesactonspecialmotifsof28SrRNAintranslationallyactivemammalribosomes.BindinganddamagingonthemotifleadstoJNKactivationandsubsequentlybiologicalresponsetothesignalinitiator,whichisnamedribotoxicstressresponse.
简介:本文就n-C4H9-Br制备实验的反应过程以及分别用KBr和NaBr制备n-C4H9-Br时出现的不同实验现象和结果进行了探讨。提出KBr的溶解速率比NaBr的溶解速率小是产生不同实验现象和结果的原因,并通过用块状NaBr进行对比实验得到验证。用块状的NaBr有利于提高n-C4H9-Br的产率。
简介:SupposethatDisaboundeddomainwithapiecewiseC^1smoothboundaryinC^n.Letψ∈C^1+α(δD).ByusingtheHadamardprincipalvalueofthehigherordersingularintegralandsolidanglecoefficientmethodofpointsontheboundary,wegivethePlemeljformulaofthehigherordersingularintegralwiththeBoehner-Martinellikernel,whichhasintegraldensityψ.Moreover,bymeansofthePlemeljformulaandmethodsofcomplexpartialdifferentialequations,wediscussthecorrespondingCauehyboundaryvalueproblemwiththeBoehner-Martinellikernelonaclosedpiecewisesmoothmanifoldandobtainitsuniquebranchcomplexharmonicsolution.
简介:Fivehumicfractionswereobtainedfromauniformly^15N-labelledsoilbyextractionwith0.1molL^-1Na4P2O7,0.1molL^-1NaOH,andHF/HCl-0.1molL^-1NaOH,consecutively,andanalyzedby^13Cand^15NCPMASNMR(crosspolarizationandmagicanglespinningnuclearmagneticresonace).Comparedwiththoseofnativesoilshumicfractionsstudiedasawholecontainedmorealkyls,methoxylsandO-alkyls,being27%-36%,17%-21%and36%-40%,respectively,butfeweraromaticsandcarboxyls(bein14%-20%and13%-90%,respectively),Amongthosehumicfractions,thehumicacid(HA)andfulvicacid(FA)extractedby0.1molL^-1Na4P2O7containedslightlymorecarboxylsthancorrespondinghumicfractionsextractedby0.1molL^-1NaOH,andtheHAextactedby0.1molL^-1NaOHaftertreatmentwithHF/HClcontainedtheleastaromaticsandcarboxyls.Thedistributionofnitrogenfunctionalgroupsofsoilhumicfractionsstudiedwasquitesimilartoeachotherandalsoquitesimilartothatofhumicfractionfromnativesoils.Morethan75%oftotalNineachfractionwasinamidefrom,with9%-13%presentasaromaticand/oraliphaticaminesandtheremainderasheerocyclicN.