简介：The(2+1)-dimensionalBKPequationintheHirotabilinearformisstudiedduringthiswork.WronskianandGrammiantechniquesareappliedtotheconstructionofWronskianandGrammiansolutionsofthisequation,respectively.ItisshownthatthesesolutionscanbeexpressedasnotonlyPfaffiansbutalsoWronskiansandGrammians.

简介：ThecaptureoforthophosphatesandtotalphosphorusfromthePudongCanalriverinthePudongDistrictofShanghaibyTiO2nanoparticlesisstudiedusingarotatingphotoreactorandthenano-TiO2photocatalystDegussaP25.TheeffectsofUVirradiationintensityinarangeof20-74mW/cm2.theloadingoftheTiO2nanoparticlesinarangeof0.05-0.1g/L,irradiationtimeupto4h,andpHvaluesinarangeof2-10.5onthecaptureefficiencyareinvestigated.TheresultsshowthatthecaptureoforthophosphatesandtotalParesignificantlyenhancedbyUVirradiation;ataloadingof0.1g/Landanirradiationintensityabove36mW/cm2,orthophosphatesandtotalphosphorusarerapidlycapturedbyTiO2nanoparticles,causinganobservedreductionfrom0.4mg/Ldownto0.02mg/L.pHvaluesinarangeof2-10.5havelittleeffectonthecaptureefficiencyoforthophosphatesandtotalphosphorus.

简介：Hierarchicalsea-urchin-shapedmanganeseoxidemicrospheresweresynthesizedviaatacilemetnoabasedonthereactionbetweenKMnO4andMnSO4inHNO3solutionat50C.Theaveragediameterofthemicrospheresis850nm.Themicrospheresconsistofacoreofdiameterof800nmandnanorodsofwidth50nm.Thenanorodsexistattheedgeofthecore.TheBrunauer-Emmett-Tellersurfaceareaofthesea-urchin-shapedmicrospheresis259.4m2/g.Apossibleformationmechanismofthehierarchicalsea-urchin-shapedmicrospheresisproposed.Thetemperaturefor90%conversionofbenzene(T90%)onthehierarchicalurchin-shapedMnO2microspheresisabout218℃.

简介：Nano-sizedhexagonalmagnesiumhydroxide（Mg（OH）2）withgooddispersibilitywassynthesizedbyadoubleinjection-hydrothermalmethod,utilizingpolyvinylpyrrolidone（PVP）asanadditiveandwithoptimizedprocessingparameters.SEMandBETanalysisshowedthatthemeanparticlesizeandspecificsurfaceareaoftheMg（OH）2particleswere174nmand50.77m2/g,respectively.TheFT-IRspectraandtheXRDpatternsshowedthatPVPwasadsorbedonthesurfaceoftheMg（OH）2crystal,thuseffectivelylimitingparticleagglomerationandhinderingcrystalgrowthalongthe（101）plane.TGAshowedadecreaseinthedecompositiontemperatureandanincreaseintheweightlossoftheMg（OH）2particlesduetoadditionofPVP.

简介：TiO2-loadedactivatedcarbonfibers（ACF）werepreparedbyahydrothermalmethod.Thesampleswerecharacterizedbyscanningelectronmicroscopy（SEM）,X-raydiffraction（XRD）,Fouriertransforminfrared（FT1R）spectrometryandUV-visdiffusereflectancespectra（DRS）.SEMimagesshowedthattheTiO2nanoparticlesweredepositedonthesurfaceofACF,andtheparticlesizeandloadingamountofTiO2werevariedbychangingtheinitialconcentrationoftetrabutyltitanate（TBOT）.TheresultsofanashexperimentshowedthattheloadingamountsofTiO2were18.4%,43.3%,52.5%,75.1%,and91.1%forinitialconcentrationsofTBOTof0.07,014,0.21,0.28,and0.35mol/L,respectively.PhysicalinteractionsplayedanimportantroleintheformationofTiO2/ACFcompositefibersthatabsorbUVandvisiblelight.ComparedwiththoseofACF,improvedadsorptionandphotocatalyticactivitytowardRhodamineB（RhB）wereobservedforTiO2/ACFcompositefiber.TheRhodamineBcouldberemovedefficientlybyTiO2/ACFcompositefibers,andtheTiO2loadingamounthadasignificanteffectonthephotocatalyticactivityofTiO2/ACFcompositefibers.

简介：Carbonnanotube（CNTs）/Fe-Ni/TiO2nanocompositephotocatalystshavebeensynthesizedbyaninsitufluidizedbedchemicalvapordeposition（FBCVD）method.ThecompositephotocatalystswerecharacterizedbyXRD,Ramanspectroscopy,BET,FESEM,TEM,UV-visspectroscopy,andXPS.TheresultsshowedthattheCNTsweregrowninsituonthesurfaceofTiO2.Fe（lll）inTiO2showednochemicalchangesinthegrowthofCNTs.Ni（Ⅱ）waspartlyreducedtometalNiintheFBCVDprocess,andthemetalNiactedasacatalystforthegrowthofCNTs.ThephotocatalyticactivitiesofCNTs/Fe-Ni/TiO2decreasedwiththeriseoftheFBCVDreactiontemperature.ForthesamplesynthesizedatlowFBCVDtemperature（500℃）,morethan90%andnearly50%ofmethylenebluewereremovedunderUVirradiationin180minandundervisiblelightirradiationin300min,respectively.TheprobablemechanismofsynergisticenhancementofphotocatalysisontheCNTs/Fe-Ni/TiO2nanocompositeisproposed.