简介：PolysaccharidecoatedPLAnanoparticlesbearingaldehydegroupswerepreparedbydialysisofDMSOsolutionofcholesterolhydrophobic-modifieddextranpolyaldehydeandPLAagainstwater.Theaveragediameterofthenanoparticleswasabout160nm,andthesizedistributionwasnearlyhomogenous.ThenanoparticleswerefunctionalizedsimultaneouslywithCD71andEGFRantibodythroughtheSchiff'sbasereaction,andthenradiolabeledwith~(99m)Tc.Afterperfusedtheradiolabelednanoparticlesintotumor-bearing...

简介：Systematicstudiesonthetreatmentandreuseoftheacidindustrialwatewatercontainingsodium2-Naphthylsulfonate(β-salt)from2-NaphthanolproductionprocessbyND-910resin(madebyself)isreportedinthispaper.Undertheoperationconditionsofinitialβ-saltconcentrationof10000-25000mg/LandinitialCODCrof20000-40000mg/L,theremovalratesofSodium2-NaphthylsulfonateandCODCrareover95%andover89%,respectively.Theeffluentcanbedischargeddirectlyafterbiologicaldegradation.TheworkingsorptioncapacityofND-910Resinforβ-saltisover230g/kg.Analkali-waterwashprocedureisutilizedtoregenerateresinandthereclaimingrateofβ-saltisover98%.

简介：Thehybridstructuresofpolystyrene-b-poly(ethyleneoxide)(PS-b-PEO)blockcopolymerandinorganicnanoparticleswithgoodstabilityandbiocompatibilityhavepotentialapplicationsindrugdeliveryandbioimaging.Sphericalco-assembliesofPS120-b-PEO318andoleylamine-cappedCdSquantumdots(QDs)areproducedsuccessfullyinthisworkbyaddingwatertoamixedcommonsolvent,suchasN,N-dimethylmethanamide(DMF)/chloroform,DMF/tetrahydrofuran(THF),orDMF/toluene.TheenergydispersiveX-ray(EDX)spectrumindicatesthatQDsarelocatedattheinterfacebetweenthecoreandshellofthesphericalco-assemblies.Theco-assemblyprocessduringwateradditionistracedbytransmissionelectronmicroscopy(TEM)andturbiditymeasurement.Sphericalco-assembliesareformedthroughbuddingfrombilayersoftheblockcopolymerandQDs.Themorphologyoftheco-assembliesisrelatedtothemiscibilityoftheQD-dispersingsolventswithwaterandthemorphologychangesfromasphericaltoavesicle-likestructurewithDMF/toluene.IncreasingTHFcontentinthemixedsolventcausesmorphologicaltransitionsfromsphericalco-assembliestomulti-branchedcylindersandmicelleswhereQDsarelocatedinthecentralcore.Increasingchloroformcontentyieldsvesicle-likestructureswithprotrudingrodsonthesurface.Themechanismofthemorphologicaltransitionsisalsodiscussedindetail.

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简介：指向nano探查基于的一个可被细菌破坏的肿瘤poly(?-caprolactone)-b-poly(ethylene乙二醇)有磁性的回声成像(MRI)的块共聚物(PCL-b-PEG)micellefunctionalized对比代理人diethylenetriaminepentaacetic酸金轧(DTPA-Gd3+)在壳上并且一在红外线附近(NIR)在为磁性的回声和光双形式的成像的核心的染料是准备。纵的relaxivity(r1)PCL-b-PEGDTPA-Gd3+，micelle是13.4(mmol/L)?1s?1，DTPA-Gd3+的三褶层，并且比有类似的结构的许多聚合对比代理人的高。在里面忍受xenografted胸肿瘤的一只裸体老鼠的光成像显示出的vivo双形式的micelle优先地经由folic在肿瘤积累了由提高的渗透和保留(EPR)效果的调停酸的活跃指向和被动累积。结果显示dualmodalitymicelle是为癌症察觉和诊断的有希望的nano探查。

简介：Lamellarcrystalsofdiblock,triblockandfour-armpoly(ethyleneglycol)-b-poly(ε-caprolactone)(PEG-b-PCL)crystalline-crystallinecopolymersweresuccessfullyobtainedfromtheirsolution.Morphologyandstructureoflamellarcrystalsofcrystalline-crystallinecopolymerswereinvestigatedusingtapping-modeatomicforcemicroscopy(AFM)andselectedareaelectrondiffraction(SAED).Allofthesesamplesshowedthetruncated-lozengemultilayerbasalshapeswithcentralscrewdislocationorcentralstack,whichwereallobtainedsimultaneouslyfromtheoilbath.ThediffractionpatternofPEGblocklamellarcrystalisattributedtothe(120)diffractingplanesandthepatternofPCLblocklamellarcrystalisattributedtothe(110)diffractingplanesand(200)diffractingplanesaccordingtotheSAEDresults.Four(110)crystalgrowthplanesandtwo(200)crystalgrowthplanesarediscoveredforthePCLblocks,butthe(120)crystalgrowthplanesofPEGblocksarehidedinthefigureofAFM.Thecrystallinestructureofthefour-armcopolymers(FA)ismoredisorderandconfusedthanthatofthediblock(DI)copolymerandthestriatedfoldsurfacestructuresoflamellarcrystalsoffour-armcopolymers(FA)aresmootherthantheseoflinearanalogues,owingtotheconfusedcrystallizationofblockscausedbythemutualrestrictionofblocksandthehindranceofthedendriticcores.Inaddition,theaspectratioofFAisgreaterthanthatoftheothers.Itishypothesizedthattherearetworeasonsforthechangeofaspectratios.First,the(200)diffractingplanesofPCLcrystalsgrewslowlycomparedtotheir(110)diffractingplanesbecauseofdifferenceintheenergybarrier.Secondly,edgedislocationsonthe(200)diffractingplanesarealsoresponsibleforthevariationoftheaspectratio.Consequently,thecrystallinedefectsareaugmentedbythecompetingblockscrystallizedsimultaneouslyandthehindranceofthedendriticcores.

简介：Wastewaterfromproductionprocessof2,3-acidwastreatedbyadsorptionusingmacroporousresinNDA-708.Afteronlyone-steptreatmentbyresinadsorption,removalefficiencyofthreekindsofnaphthalenechemicalswasabove99%;removaleficiencyofCODcrwasabove96%.Underproperoperatingcondition,desorptionefficiencywasaround100%.Therunningrecordsoftheindustrialfacilityshowedthatthenaphthlenechemicalsindesorptioneffluentcouldbereusedwithoutobviousinfluenceonthequalityoftheproduct.

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简介：Usingpolyvinylalcohol(PVA)asrawmaterialandvacuumpumpoilasoilphasemedium,PVA-basedmicrocarrierswerepreparedbysuspensionmethodThediametersofthebeadswere100-180μm.LO2cellswereculturedonPVA-basedmicrocarriersandcytodexⅢmicrocarriers.Morphology,attachmentandgrowthrateofLO2cellswerestudied.

简介：TiO_2-coatedpolystyrenenanoparticleswerepreparedinasimpleway.First,functionalPSparticlesweresynthesizedbycopolymerizingonekindofpolymerizablesurfactantwithstyrene.Thenthestabledispersionsofpolystyrenenanoparticleswereusedastemplates,andpolystyrenenanoparticleswerecoatedwithtitaniabyinsituhydrolysisoftetra-n-butyltitanate(TBT).Nosurfacetreatmentandcentrifugation/redispersioncycleprocesswereneededduringthewholeexperiment.IsolatedPSsphereswithuni...

简介：Fourkindsofpalladiumcatalystsdispersedonpoly-N-vinyl-2-pyrrolidonewerepreparedbyusingCH3OH-NaOH,NaBH4,H2OorCH3OH-H2Oasthereducingagentintheprocessofcatalystpreparation.ThecatalystswerecharacterizedbyXPS,TEM,XRDandusedforthehydrogenationofmethylacrylate.Itwasfoundthatthevalencestateofpalladiumanddistributionofpalladiumparticlesaswellasthehydrogenationrateweregreatlyaffectedbythereducingagent.ThebestevenlydispersedpalladiumcatalystshowinghighhydrogenationactivitywaspreparedusingCH3OH-NaOHasthereducingagent.

简介：Anewkindofmonomerswassuccessfullysynthesizedbythereactionbetween2-chloromethylcycloketalandtrimethylsilylcyanide,followedbyringclosureanddehaiogenation.Polymerizationsofthemonomerswerecarriedoutinbenzenesolutionat80℃withbenzoylperoxideasinitiator.BoththestructuresofmonomersandpolymerswerecharacterizedbyIR,1HNMR,13CNMRandelementalanalysis.

简介：DistributionofmetalsonPd-SnO2/D3520catalystsandstateofthecatalystswrerstudiedwithSEM,XRD.TheinteractionbetweenmetalsandsupportorbetweenPdandSnorPbwerestudiedbyIR,XPS.Inaddition,therelationshipoftheactivityforcatalytichydrogenationoftheolefinsandouterlayervalenceelectrondensityofPdwasdiscussed.Theresultsshowedthatthesecatalystshadsuitablesurfacestate,themetalswereuniformlydispersedonthesurfacelayerofthesupport.Therewerenotobviousinteractionbetweenthemetalsandthesupport.TherewasstronginteractionbetweenPdandSn(orPb)inthecatalysts.ThecatalyticactivityforhydrogenationwasrelatedtoouterlayervalenceelectrondensityofPd.

简介：DistributionofmetalsonPd-SnO2/D3520catalystsandstateofthecatalystswerestudiedwithSEM,XRD.TheinteractionbetweenmetalsandsupportorbetweenPdandSnorPbwerestudiedbyIR,XPS.Inaddition,therelationshipoftheactivityforcatalytichydrogenationoftheolefinsandouterlayervalenceelectrondensityofPdwasdiscussed.Theresultsshowedthatthesecatalystshadsuitablesurfacestate,themetalswereuniformlydispersedonthesurfacelayerofthesupport.Therewerenotobviousinteractionbetweenthemetalsandthesupport.TherewasstronginteractionbetweenPdandSn(orPb)inthecatalysts.ThecatalyticactivityforhydrogenationwasrelatedtoouterlayervalenceelectrondensityofPd.

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简介：TheNdCl3/MgCl2bisupportedcatalystwaspreparedbyusingNdCl3,MgCl2,（CH3）2（CH2）2OHandTiCl4.ItisshownthatthestructureofbisupportedcatalystwasdifferentfromthoseofeitherNdCl3orMgCl2singlesupportedcatalyst.Apeculiartypeofkineticcurveforethylenepolymerizationwasfound.

简介：Polyfluoroalkylsubstituted2-hydroxyethylacrylate6wassynthesizedinsixstepsusingglycerolasastartingmaterial.Apreliminaryinvestigationhasbeentakenonthesynthesisandcharacterizationofcopolymersof6and2-hydroxyethylmethacrylate.

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