简介:ThemolecularsieveVPI-5wassynthesizedbyusingvariousorganicamines(DEA,Di-PA,DBA,DPenA,TBA,DEOAandTEOA)asthestructure-directingagent.TheuseofDPAenlargedtherangeofthecrystallizationtemperaturefrom110℃to190℃inthesynthesisofVPI-5,whiletheuseofTEOAchangedthecompositionofthereactantsinabroadvariety.DiaminesarethetypicalaminesinthesynthesisofVPI-5.AmongthemDBAandDPAarethemostfavoritestructure-directingagentsforthesynthesisofVPI-5molecularsieve.
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:采用水热合成方法构建了基于Preyssler型多酸[S5W30O110]的有机-无机杂化材料,其分子式为[HKS5W30O110]·(2,2-Hbpy)8·2H2O(1,bpy=bipyridine).单晶X-射线衍射分析表明化合物1是由S-中心的Preyssler型多酸作为模版,被2,2-联吡啶分子包围形成的核壳结构的有机无机杂化材料.这是第一例基于S-中心Preyssler型多酸的超分子核壳结构.其中质子化的2,2’-联吡啶有机基团通过静电作用与Preyssler型多酸分子构筑成有机无机杂化材料.该化合物属于三斜晶系,空间群为P-1.晶胞参数:a=1.79505(2)nm,b=1.83478(2)nm,c=4.12816(4)nm,α=85.0610(10)°,β=80.6160(10)°,γ=60.7210(10)°,晶胞体积为11.7002(2)nm3.
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.