简介:Aseriesof5-aminolevulinicacidanditsalkylestermethanesulfonateswasexploitedtophotodynamictherapy(PDT)ofhumanlymphocyticcells,U-937invitro.ThePDTefficiencyisinfluencedbytheconcentrationandincubationtime.Generally,forALAanditsalkylestermethanesulfonates,thecellsurvivalratedecreasesandtheaccumulationabilityofPpIXincreaseswiththeconcentrationandincubationtime.Wefoundthatthelongercarbonchainmethanesulfonates(C5-S,C6-S,C8-S)exhibitbetterPDTeffectthanALAmethanesulfonate.ThispossiblyprovidesapromisingroutetotheclinicalapplicationofPpIX-mediatedPDTtocancercell.
简介:4,4-Dialkyl-2-oxazolin-5-onesarepreparedbyonestepreactionof2-oxazolin-5-onewiththemagnesiummethylcarbonate(MMC)andalkyIhalides.Itisanovelandconvenientmethodforsynthesisofα,Υ-disubstitutcdα-aminoacidbyhydrolysisof4,4-dialkyl-2-oxazolin-5-ones.
简介:TheexternalsurfaceofHZSM-5zeolitewaspassivatedbyliquidsiliceousdepositionandbyacidicsitespoisoningwithlepidine,respectively.Thenmethanol-to-hydrocarbons(MTH)reactionwasinvestigatedovertheaboveas-preparedcatalystsandthedissolublecokeontheseusedcatalystswasanalyzedbyGC-MS,tostudytheroleoftheexternalsurfaceofHZSM-5inthecatalyticreaction.ComparisonwiththeexperimentalresultsbasedonparentZSM-5showedthattheproductdistributionofMTHreactionwasobviouslyinfluencedbytheexternalsurface.Evidenceswerelistedasfollows:(1)thefinalproductonparentHZSM-5showedhigheraromaticselectivity,lowerolefinselectivity,lowerratioofC2/C3+aliphaticsandhigherratioofC3/C4+aliphaticsthanthereactionmixtureproducedbythesolecatalysisofacidicsitesinHZSM-5channel;(2)alittleofpentamethylbenzeneandhexamethylbenzeneintheproductonparentHZSM-5,wasproducedviamulti-methylationofmethylbenzeneontheexternalsurface.TheaboveconclusionmayalsobesuitableforMTHreactionoverotherzeoliteswith10-ringchannel.
简介:为它的高氧化抵抗,钇硅酸盐是为在在1600°C上面的温度的carbon-fiber-reinforcedcomposites的保护的涂层的一个重要候选人。一个新奇方法,由一起沉淀组成,弄干水花,热处理和plasma-densification,被开发准备Y2SiO5粉末为热喷洒。作文,形态学和综合Y2SiO5粉末的流动能力被XRD,SEM和霍尔流量计分别地调查。结果证明综合Y2SiO5粉末与高纯净是将近球形的。分别地,Y2SiO5粉末的明显的密度和流动能力是1.87g/cm3和37s/50g它为大气的血浆喷洒导致多达80%的高免职效率。
简介:π-/π+ratiowasfoundtobeasensitiveprobetothehigh-densitybehaviorofthesymmetryenergybyusingseveraltransportmodels.However,asshowninFig.1,atbeamenergiesbelowthepionproductionthreshold,theeffectsofin-mediumnucleon-nucleonscatteringcrosssection(whichisstillcontroversial)stronglyaffectthevalueofπ??/π+ratio[1].Itisthusnecessarytodoacomparativestudyoftheeffectsofthein-mediumNNcrosssectionandtheeffectsofthesymmetryenergyonpionproductioninheavy-ioncollisionsatlowerbeamenergies.
简介:STUDYONTHEREARRANGEMENTREACTIONOF5-AMINO-1-AMINOCARBONYL-1,2,ANDITSANALOGUES¥RongJianLU;HuaZhengYANG;BaoYingQIAN;HaiYanDENG(N...
简介:ThecokedepositiononHZSM-5/SAPO-34compositecatalystshasbeenstudiedintheconversionofethanoltopropylene.TheHZSM-5/SAPO-34compositecatalystsweresynthesizedbyhydrothermalmethod(ZS-HS)andfullyblending(ZS-MM).TheusedcatalystswerecharacterizedbyXRD,N2adsorption–desorption,TGA,TPO,elementalanalysis,FTIRandXPS.ThecokingkineticsonbothZS-HSandZS-MMhasbeeninvestigatedandtheircokingrateequationswereobtained.TheusedZS-MMcatalysthadhigheramountofcokeandlowernC:nHthantheusedZS-HS.90%ofthecokewasdepositedinthemicroporesofZS-HS,whilealmost45%ofthecokelocatedinthemicroporesofZS-MM.ThecokedepositedonZS-HScatalystwasmainlygraphite-likecarbonspecies,whereasdehydrogenatedcokespecieswasthemajoronZS-MM.ThecokingactivationenergyofZS-MMwaslowerthanthatofZS-HS,andthecokingrateonZS-MMwasfasterthanonZS-HS.Inaddition,theregenerationofZS-MMcatalystshowedthatithadagoodhydrothermalstability.Thedifferencesoncokingbehaviorsonthetwocatalystswereduetotheirdifferentacidicpropertiesandtextures.
简介:Highqualitypoly(5-cyanoindole)(P5CI)filmswereelectrosynthesizedbydirectanodicoxidationof5-cyanoindoleonstainlesssteelsheetinthemixedelectrolytesofborontrifluoridediethyletherate(BFEE)anddiethylether(EE)(byvolume1:1)+0.05molL~(-1)Bu_4NBF_4.Thefilmformedcanbepeeledofftheelectrodeintofreestandingfilms.TheadditionofEEintoBFEEcanimprovethesolubilityofmonomer.P5CIfilmsobtainedfromthismediumshowedexcellentelectrochemicalbehaviorwithconductivityof10~(-2)Scm~(-1).Structuralstudiesshowedthatthepolymerizationof5-cyanoindoleoccurredatthe2,3position.As-formedP5CIfilmswerethoroughlysolubleinstrongpolarorganicsolventdimethylsulfoxide(DMSO)whilepartlysolubleintetrahydrofuran(THF)oracetone.FluorescencespectralstudiesindicatedthatP5CIwasagoodblue-lightemitter.
简介:Zn/ZSM-5(NZ2)andZn/Ni/ZSM-5(NZ3)asthecatalystsformethanoltoaromatics(MTA)weresynthesizedbyasimpleultrasonicimpregnation.ThetexturalandacidpropertiesofallcatalystswerecharacterizedusingXRD,HRTEM,NH3-TPD,Py-IR,XPS,XRFandTGtechniques.TheXRDandHRTEMresultsshowedthatthebasiczeolitestructureswerenotaffectedmuchwiththeincorporationofZnandNispecies.However,greatchangeshavetakenplaceinacidproperties.ThePy-IRandXPSresultsindicatedthattheZn-Lewisacidsites(ZnOH+species),whichhavestrongerinteractionwiththezeoliteframeworkcomparedwithZnOspecies,weregeneratedattheexpenseofBacidsiteswiththeincorporationofzincspecies.Moreover,theproductanalysisresultsshowedthattheincorporationofzincspeciespromotedtheprimaryaromatizationbyenhancingthedehydroaromatizationandsuppressingthecrackingandsubsequentH-transferreaction.Furthermore,theadditionofNispecieswellinhibitedthelossofzincspeciesbyconvertingpartialZnOspeciestoZnOH+species,andthusimprovedthearomatizationactivityandcatalyststability.ThecatalyticperformanceresultsshowedthattheNZ3possesshigherconversionofmethanolinalongertimeandloweraveragerateofcokeformationcomparedwithNZ2.Inaddition,theNZ3alsoexhibitedthehighestyieldofBTXasthereactionproceeds.
简介:Polymer-supportedRCpCpTiCl2(Cp=η^5-C5H4;RCp=η^5-RC5H4)havebeenpreparedandreducedbyi-C3H7MgBrinsitu,thenusedincatalyticisomerizationof1,5-hexadiene.Theisomerizationof1,5-hexadieneleadstoamixtureofcyclicandlinearproducts.Theratioofcyclictolinearproductdependsonthenatureofthesupporterandthesubstituentonthecyclopentadienylring.Theformercontributesthemost,forexample,silicasupportedCp2TiCl2gavecyclic-linearratioof99/1,whileforpolymer-supportedCp2TiCl2species,linearcompoundsarethemajorproductsandtheratioofcyclictolinearproductchangeswithdifferentRgroupsonthecyclopentadienylring.
简介:CarbondepositionduringmethanoltohydrocarbonsleadstothequickdeactivationofZSM-5catalystanditisoneofthemajorproblemsforthistechnology.DecreasingthecrystalsizeorintroducingmesoporesintoZSM-5zeolitescanimproveitsdiffusionpropertyanddecreasethecokeformation.Inthispaper,nano-sizedZSM-5zeolitewithintercrystallinemesoporescombiningthemesoporousandnanosizedstructurewasfabricated.Forcomparison,themesoporousZSM-5andnano-sizedZSM-5werealsoprepared.ThesecatalystsampleswerecharacterizedbyXRD,BET,NH3-TPD,TEM,Py-IRandTGtechniquesandusedontheconversionofmethanoltogasolineinafixed-bedreactoratT=405°C,WHSV=4.74h-1andP=1.0MPa.Itwasfoundthattheexternalsurfaceareaofthenano-sizedZSM-5zeolitewithintercrystallinemesoporesreached104m2/g,largerthanthatofmesoporousZSM-5(66m2/g)andnanosizedZSM-5(76m2/g).Catalyticlifetimeofthenano-sizedZSM-5zeolitewithintercrystallinemesoporeswas93h,whichwasonlylongerthanthatofmesoporousZSM-5(86h),butshorterthanthatofnanosizedZSM-5(104h).Strongaciditypromotedthecokeformationandthusdecreasedthecatalyticlifetimeofthenano-sizedZSM-5zeolitewithintercrystallinemesoporesthoughitpresentedlargeexternalsurfacethatcouldimprovethediffusionproperty.Thespecialzeolitecatalystwasfurtherdealuminatedtodecreasethestrongacidity.Afterthis,itscokeformationratewasslowedandcatalyticlifetimewasprolongedto106hbecauseofthelargeexternalsurfaceareaanddecreasedweakacidity.Thisspecialstructuralzeoliteisapotentialcatalystformethanoltogasolinereaction.