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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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简介：Thisworkdealswiththekineticsofco-condensationpolymerizationofAB2andABmonomers,givingexpressionsofthetwo-dimensionalmolecularweightdistributionfunctionandthenumber/weightaveragemolecularweightsoftheresultingcopolymers.Thetwo-dimensionalmolecularweightdistributiondependsontwoindices,nandl,whicharetherespectivenumbersofAB2andABunitsinacopolymerspecies.Theevolutionofthetwo-dimensionalweightandzdistributionsduringtheco-condensationpolymerizationhasbeenevaluatedsystematically.Finally,thetwo-dimensionaldistributionwastransformedintoaone-dimensionalmolecularweightdistributionwithonlyonevariable(themolecularweightoftheproductsinsteadofthedegreeofpolymerization).Thecalculatedresultsshowthatthehighlybranchedcopolymerhasaverybroadmolecularweightdistributionwhentheco-condensationpolymerizationapproachescompletion.

简介：2－Hydroxyethylacrylateissynthesizedfromacrylicacidandethyleneglycolunderasimpleandmildconditionbyusingstrongacidiccationionexchangeresinasacatalyst,whichcouldberecycledaslongas10timeswithhighactivation.

简介：TheanalyticalexpressionsofthevariousstructuralunitsandtheaveragedegreeofbranchingforthehyperbranchedpolymersresultedfromAB_2polycondensationwithsubstitutioneffectwerederivedbythekineticmechanism.ThereactivitydifferencebetweentheBgroupinlinearunitandthatinterminalgrouphasgreateffectonthemolecularparametersoftheproductsobtained.TheconcentrationofterminalunitshasamaximumwiththeincreaseoftheconversionofAgroups(x).Thehigherthereactivityratio(r)oflinearBgrouptobranchedoneis,thelaterthemaximumappearsandthelargeritis.Thedegreeofbranchingofthehyperbranchedpolymersobtainediscontrollablebyadjustingtheparametersofrandx,whichincreaseswithincreasingbothxandr.

简介：在这个工作，综合体新热地稳定(amide-imide)poly，有在n丁基甲基imidazolium溴化物的悬挂的2-pyridyl-1,3,4-oxadiazole单位的s作为反应媒介被报导了。新二羟基的酸从肼的反应被导出，2-(5-(3,5-diaminophenyl)-1,3,4-oxadiazole-2-yl)pyridine(POBD)，和trimellitic酸酐。聚合物在丁基甲基imidazolium溴化物从diimide二酸(DIDA)和不同的芳香的肼的反应被准备，[bmim][Br]，面对triphenyl亚磷酸盐(TPP)作为没有需要任何额外的部件的压缩代理人。poly准备了(amide-imide)s被FTIR描绘，元素的分析，并且通过模型混合物的合成。准备聚合物是可溶的在极并且aprotic溶剂例如DMF，DMSO，NMP和DMAc。聚合物答案的固有的粘性在在0.125g/dL的集中在集中的H2SO4测量在的0.521.33dL/g的范围(25

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简介：Thesemibatchemulsifier-freeemulsioncopolymerizationofmethylmethacrylate(MMA)andbutylacrylate(BA)inthepresenceof2-hydroxyethylmethacrylate(HEMA)initiatedbyK2S2O8(PSP)wasstudied.Thelatexparticlescanmaintainanappreciablestabilityduringtheemulsifier-freeemulsioncopolymerizationofMMAandBAinthepresenceofHEMA.Theaverageparticlediameterincreasewithanincreaseoftotalsolidscontent,HEMAcontent,PSPcontent,ionicstrengthofthesystemandmonomerfeedrate,anddecreasewiththemonomerfeedrationfrom3/1(MMA/BA:molarration).to1/3.ThestabilityofthisreactionsystemisimprovedbyaddingHEMAasnonioniccomonomer,Highsolidscontent(50%)latexwithmonodisperseparticlecanbeobtainedusingthisprocess.

简介：CuO/γ-Al2O3catalystswerepreparedbyplasmatreatmentandconventionalimpregnationmethods.Thecatalyticcombustionoftwokindsofvolatileorganiccompounds(VOCs),tolueneandbenzene,werecarriedoutovertheseCuO/γ-Al2O3catalysts.ThesurfacepropertiesofthesecatalystswerecharacterizedbyX-rayDiffraction(XRD)andScanningElectronMicroscopy(SEM).TheexperimentalresultsshowedthatincatalyticcombustiontheactivityoftheCuO/γ-Al2O3catalystpreparedviaplasmawasmuchhigherthanthatoftheCuO/γ-Al2O3catalystpreparedbyconventionalimpregnationmethod.XRDresultsshowedthatanenhanceddispersionhadbeenachievedwiththeplasmatreatment.SEMresultsindicatedthatthesizebecamemuchsmallerandthesurfacebecamemoreuniformwiththeplasmatreatment.

简介：ThepaperintroducesthepreparationoffloatingTiO2/beadsphotocalystattachedtothehollowglassmicro-beadssurfacebysol-geltechniqueusingtetrabutyltitanateasmaterialandthepreparationoffloatingCoPcS/TiO2/beadsbydip-coatigtechnique.TheoptimalfactorofdegradationofvegetableoilfloatingonwaterusingCoPcS/TiO2/beadswasstudied.Theresultshowedthattheremovalrateofvegetableoilfloatingonwatercanhighlyreach90%attheoptimalcondition(acidityorneutrality,375Wmedium-pressuremercuryvapourlamp,illumination2h~3h,1gCoPcS/TiO2/beads).ThephotocatalyticremovalefficiencycausingbyCoPcS/TiO2/beadswasincreasedrapidlybyaddingatraceamountofH2O2.

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：Thetreatmentandresourcereuseof1,2,4-acidproducingwastewaterbyself-mademacroporousadsorptionresinND,A-107wasstudiedinthispaper.Optimumadsorptionanddesorptionprocessparameterswereacquiredbysystematicallystudy.ThepolymericresinNDA-107indicatedgoodadsorption&desorptionof1,2,4-acidinthewastewater.Theremovalefficiencyof1,2,4-acid,CODerisabout78%,72%respectively.Itisevidentthatthisadsorptionprocessisanefficienttreatmentmethodfor1,2,4-acidproducingwastewater.Atthesametime,theaccumulationandresourcereuseofl,2,4-acidcanberealizedinthisprocess.

简介：Inthiswork,DSCandSEMstudiesindicatethation-ligandinteractioncanbeutilizedtoenhancetheinteractionofpoly(styrene-block-2-vinylpyridine)[P(S-b-2VP)]andpolyethylenebasedionomer(Surlyn).Thecompatibilityforthisblendingsystemcanbeimprovedbythisspecialinteractionand20/80wtistheoptimumblendingcompositionwithgoodcompatibility.FTIRresultsfurthercertifythatstronginteractionsexistintheblendingsystem.

简介：Anovelhydrophilicnanocompositeadditive(TiO2-g-PNIPAAm)wassynthesizedbythesurfacemodificationoftitaniumdioxide(TiO2)withN-isopropylacrylamide(NIPAAm)via"graft-from"technique.Andthenanocompositemembraneofpoly(vinylidenefluoride)(PVDF)/TiO2-g-PNIPAAmwasfabricatedbywetphaseinversion.Thegraftdegreewasobtainedbythermo-gravimetricanalysis(TGA).Fouriertransforminfraredattenuatedreflectionspectroscopy(FTIR-ATR)andX-rayphotoelectronicspectroscopy(XPS)characterizationresultssuggestedthatTiO2-g-PNIPAAmnanoparticlessegregatedonmembranesurfaceduringthephaseseparationprocess.Scanningelectronmicroscopy(SEM)wasconductedtoinvestigatethesurfaceandcross-sectionofthemodifiedmembranes.ThewatercontactanglemeasurementsconfirmedthatTiO2-g-PNIPAAmnanoparticlesendowedPVDFmembranesbetterhydrophlilicityandthermo-responsivepropertiescomparedwiththoseofthepristinePVDFmembrane.Thewatercontactangledecreasedfrom92.8°ofthePVDFmembraneto61.2°ofthenanocompostiemembrane.Bovineserumalbumin(BSA)staticanddynamicadsorptionexperimentssuggestedthatexcellentantifoulingpropertiesofmembraneswasacquiredafteraddingTiO2-gPNIPAAm.ThemaximumBSAadsorptionat40°Cwasabout3timesthanthatat23°C.ThepermeationexperimentsindicatedthewaterfluxrecoverratioandBSArejectionratiowereimprovedatdifferenttemperatures.

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简介：Asupercriticalcarbondioxide(ScCO2)assistedphaseinversionwasdevelopedtoproducemicroporouspoly(vinylidenefluoride)(PVDF)membraneswhosemorphologycharacteristicsarisefrombothliquid-liquiddemixingandsolid-liquiddemixing(crystallization).ThisresultwasconfirmedbyFouriertransforminfraredspectroscopy(FTIR),fromwhichbothαandβcrystalswerefound.Asrevealedbycontactangleexperiment,thePVDFmembranespreparedviaScCO2assistedphaseinversionweremorehydrophobiccomparedwiththecontrolmembraneproducedviaconventionalimmersionprecipitationtechnique.Inparticular,thesamplewith15wt%PVDFpreparedat45°Cand13MPaexhibitedacontactangleof142°,whichwasmainlycausedbythemultilevelmicro-andnano-structure.Theeffectsofpolyethyleneglycol(PEG),polyvinylpyrrolidone(PVP)andlithiumchloride(LiCl)onthestructuresandcrystalformwereinvestigated.PVPpromotedtheformationofβphasecrystalform,whilePEGbooststheevolutionofαphase.LiClrestrainedthecrystallizationdegreeofPVDFmembraneunderScCO2.

简介：penta醚混合物被di(trimethylolpropane)的反应作为烷基卤化物作为强壮的底和甲基碘化物与钠氢化物综合。这混合物被NMR，FTIR，和GC技术描绘。MgCl2-supported钛催化剂与作为内部施主改变penta醚化合物的数量被合并，也，没有内部施主的催化剂被综合。综合催化剂和常规Ziegler-Natta催化剂被描绘。钛内容被spectrophotometry决定，由由argentometric滴定的complexometric滴定和氯化物的镁。有准备MgCl2-supportedZiegler-Natta催化剂的丙烯聚合上的新内部施主的效果被调查然后这些结果与用常规diisobutylphthalate-besed-Ziegler-Natta催化剂获得的结果相比。聚丙烯的最高的crystallinity度，融化的温度，和isotacticity与penta-ether/Mg用催化剂被获得臼齿的比率平等者到0.21。