简介:TheantibacterialeffectofcarryingsilverB2O3-SiO2-Na2Oglassmaterialwasstudiedbymeansofantibacterialring,nephelometery,MICvalue,thinfilmattachmentandmicrocalorimetry,respectively.TheexperimentalresultsoffivekindsofantibacterialtestmethodsarealmostidenticalandcanverifythatcarryingsilverB2O3-SiO2-Na2Oglassmaterialexertsanexcellentantibacterialperformance.Antibacterialringandnephelometeryaresimple,quick,buttheprecisionisrestrictive.MICvalue,thinfilmattachmentmethodandmicrocalorimetrycanquantitativelycomparetheantibacterialeffectsoftheantibacterialglassmaterial.Comparedwiththetraditionalmicrobetestmethods,themicrocalorimetrycananalyzetheinhibitingeffectofthecell'sgrowthandmetabolismontheantibacterialglassmaterialbymonitoringthethermaleffectcontinuouslyandautomatically.
简介:Theimplantedionrange,thedepthprofileandthefilmsttuctureoftheimplantedlayerwerestudied;thecarrierconcentrationandthemobilityweremeasured;theconductivitymechanismofthefilmimplantedFeintoAl2O3ceramicwasdiscussed.TheconclusionisthattheimplantedFe2+ionsmoveintoAl2O3latticeandreplaceAl3+toformsubs-titutionimpuritiessothattheionimplantedlat-tice,ascomparedwiththeoriginalone,presentsaneffectivenegativechargewhichformsanegativechargecenter.Avacancyisboundarroundit,andanacceptorisintroducedintheforbiddenband.
简介:Thevolatilizationkineticsofantimonytrisulfideinsteamatmospherewasstudiedwiththermogravimetryattemperaturesfrom923to1123K.Atheoreticalmodelwasdevelopedtocalculatetheoverallrateconstantandthemasstransfercoefficientingasphases.Theexperimentalresultsshowthatthevolatilizationrateisenhancedwithincreasingtemperatureandsteamflowrate.Thevolatilizationrateismainlycontrolledbythemasstransportingasphases.Theapparentactivationenergyfortheprocessisfoundtobe59.93kJ/mol.ItisdemonstratedthatSb2S3isdominantlyoxidizedintoSb2O3andH2Sbywatervaporinthevolatilizationprocess.Someantimonymetalisformed.Thereactionmechanismisdiscussedinaccordancewithexperimentaldata.
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简介:TiB2ceramicspowderwassynthesizedfromB2O3-TiO2-Mgsystem.TheeffectsofTiB2additionasdiluentonthecombustionsynthesisprocesswereinvestigated.TheresultsofthermodynamiccalculationandexperimentsshowthattheincreaseofTiB2contentrangingfrom0to20wt%canreducetheadiabatictemperatureTadfrom3100Kto2896KandcombustiontemperatureTcfrom2139Kto1621Krespectively.TheparticlesizeandhalfwidthoftheparticledistributionarealsoincreasedwiththeadditionofTiB2increasingfrom0to20wt%.ThecombustionproductisamixtureofTiB2,MgO,andotherintermediatephases.TheleachedproductcontainsmainlyTiB2,TiO2andTiN,anditsoxygencontentis7.77wt%.
简介:Anitrate-citratecombustionroutetosynthesizeLa0.9Sr0.1Ga0.8Mg0.2O3-δpowderforsolidoxidefuelcellapplicationwaspresented.Thisrouteisbasedonthegellingofnitratesolutionsbytheadditionofcitricacidandammoniumhydroxide,followedbyanintensecombustionprocessduetoanexothermicredoxreactionbetweennitrateandcitrateions.TheoptimumtechnicalparametersarethatthepHvalueis5,andthemolarratioofcitricacidtothetotalmetallicionis1.5:1.X-raydiffractioncharacterizationofcalcinedgelshowsthatpurephasewassynthesizedaftercalcinationat1400℃for10h,andtheTEMresultshowsthecalcinedpowderwithaverageparticlesizeisabout150nm.Thegrainresistancecontributestothetotalresistanceofsinteredpelletbelow500℃.Theconductivityofthesinteredpellentat800℃was0.07S-1.cm-1higherthantheconductivityofYSZ(0.05S-1.cm-1at800℃)
简介:Manganesephthalocyanine(MnPc)-Fe3O4nanoparticlescompositewaspreparedandcharacterized.TheresultsshowthatMnPcarecompletedonthesurfaceofFe3O4nanoparticlesinthestateofsinglemolecule.ThereiseffectivecompositebetweenMnPcandFe3O4nanoparticleswhichcanimprovetheantioxidizationabilityofFe3O4nanoparticlesgreatly.Thecompositewasdispersedintochlorinatedparaffinoiltoformelectromag-netorheological(EMR)fluidwithhighactivity,andtheEMRpropertiesofthisEMRfluidarestudied.
简介:Aone-pot,solvent-thermalprocesswasusedtocreatetheultrafineZnFe2O4nanoparticlesphotocatalyst.Duringthesolvent-thermalprocess,theinsituself-formingNaClnotonlyservedasa"cage"toconfinetheiondiffusion,butalsoactedasamicroreactorfornanocrystallitegrowth.Anaverageparticlesizeof~10nmandahigh-specificsurfaceareaof~112.9m2/gwereobservedfortheultrafineZnFe2O4nanoparticlesOwingtothesynergisticeffectofultrafineparticlesize,thefullutilizationofthevisiblelightregionandhighconductionband(CB)position,ultrafineZnFe2O4photocatalystdisplayedanefficientphotocatalyticCO2reductionundervisiblelightillumination.Besides,theultrafineZnFe2O4photocatalystshowedhighproductionselectivityforCH3CHOandC2H5OHgenerationinaqueousCO2/NaHCO3solution.Thisworkmayprovideanewideaforthesynthesisofnewhigh-efficiencyphotocatalysts.
简介:Sodiumparanitrophenolatedihydrate(NPNa·2H2O)isanexcellentsemiorganicnonlinearoptical(NLO)material,crystallizesbothinwaterandmethanolwithhighdegreeoftransparency.Goodopticalqualitysinglecrystalsofdimensionupto18mmx6mmx3mmareobtainedbyisothermalsolventevaporationtechnique.Thesolubilityofthecrystalindifferentsolventswasmeasuredgravimetrically.ThesinglecrystalsofNPNa·2H2Oshowvariationinphysicalpropertiesandgrowthrateindifferentsolvents.Methanolorethanolsolutionyieldscrystalsofbipyramidalshapewithclearmorphology.However,methanolgrowncrystalisexhibitingimprovedhardnessparametersandpossessesexcellentthermalstabilityascomparedtowatergrowncrystals.TheeffectsofsolventonhardnessparameteralongwiththermalandopticalpropertiesofNPNa·2H2Owasrevealedinthispaper.
简介:Basedonthedifferenceofhydroxygroupconfigurationondifferentplanesofα-Fe2O3nanoparticles,usingthespecialadsorptionandcoordinationofphosphateonthe(001)planeofα-Fe2O3,well-crystallizedandwelldispersedα-Fe2O3nanodiskswithdiameterof150–200nmandthicknessof40–80nmweresynthesizedviaahydrothermalmethod.Themagneticpropertiesofsynthesizednanodiskswereinvestigated.Itwasfoundthatthenanodiskspossessedasaturationmagnetization(Ms)of0.38emu/g,aremanentmagnetization(Mr)of0.031emu/gandacoercivityof452.91Oeatroomtemperature.TheMrandcoercivityofsynthesizedα-Fe2O3nanodisksarehigherandtheMsislowerthanthoseofotherpreviouslyreportedα-Fe2O3nanostructures.
简介:MoleculardynamicssimulationusingauniversalforcefieldhasbeenemployedtodeterminethediffusioncoefficientsofO2andNa2SO4vaporintoB2O3andSiCfrom700Kto1273K,respectively.Einsteindiffusionwasobservedina250~300pssimulation.ThediffusioncoefficientfortheO2rangefromabout9.279×10-9cm2/sforB2O3to2.275×10-10cm2/sforSiCataloadingof32moleculespersimulationbox,thatfortheNa2SO4vaporrangefromabout9.888×10-7cm2/sforB2O3to1.837×10-10cm2/sforSiCataloadingof8moleculespersimulationbox.EnvironmentpropertiesofC/SiCcompositewillbeincreasedviatheB2O3preventingthediffusionofO2andNa2SO4vaporintothepyrolyticinterphaseandcarbonfibers.