简介：Theadsorptionbehaviorofionicgoldontochelatingfibercontainingamidoximegroupswasinvestigated.ThechelatingfiberpresentshighadsorptioncapacityforionicgoldAu^3+（upto626mg/g,whenthecontentofamidoximegroupreaches7.59mmol/g),andpossessestheabilitytoreducetheAu^3+intometallicgold,Intheredoxprocess,theamidoximegroupisoxidizedintocarboxylgroup.

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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：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。

简介：Thestructureofpolyimidefrom1,4-bis(3’,4’-dicarboxyphenoxy)benzeneand4,4’-oxydianilinefilmspecimensbeforeandafterhotstretchinghasbeeninvestigatedbyWAXD,DSCandFTIR.AsevidencedbyboththeWAXDandDSCresults,itcouldbebelievedthatstraininducedcrystallizationdidtakeplaceafterhotstretching.Meanwhile,shiftingpositionandsplittingofsomebandpeaksexistedontheFTIRspectrogramswereexplainedintermsoftheclosepackingofchainsandthechangesofinter-molecularcharge-transferinteractionbetweenimidegroupsandaromaticgroupsuponcrystallization.

简介：TiCl_4/MgCl_2/claycompoundcatalystwaspreparedbychemicalreaction.Exfoliatedpolypropylene(PP)/claynanocompositesweresynthesizedbyinsitupolymerizationwiththiscompoundcatalyst.Effectsofpolymerizationtemperature,polymerizationtime,propylenepressure,solventconsumptionandpre-treattimeofcatalystoncatalystactivityandcatalyticstereospecificitywerestudied.Underoptimalconditions,activityofthenano-compoundcatalystisabout88.3kg/(molTi·h).IsotacticityofPPobtainedinthenanocompositesisintherangeof89%-99%,anditsmeltingtemperatureisabout159℃.Theweight-averagemolecularweightofPPcanreach6.7×10~5-7.8×10~5,andthemolecularweightdistributionisbetween7.7and7.9.

简介：Anewdi-functionadsorbent(JN-3)waspreparedbysulfhydrylmodified.ComparingwithAmberliteXAD-4andNDA-150,theequilibriumadsorptionforphenolontheJN-3fromaqueoussolutionswastested,perfectadsorptioncapacitywasshown.Pb2+canbealsoremovedbyJN-3becauseofthechelateinteractionbetweensulfhydrylgroupsandmetalions.Thisadsorbentcouldbeusedinremovalofcombinepollutantssuchasphenoliccompoundsandheavymetalionsfromwastestreams.

简介：新印离子的聚合物(IIP)被4-vinylpyridine(单体)的copolymerization综合，ethyleneglycoldimethacrylate(cross-linker)和2,2-azobis-isobutyronitrile(开始者)面对Cd2+和quinaldic酸(complexing代理人)。IIP和空白的聚合物的吸附能力分别地是45.0和6.2mgg1，这被发现。为不同二进制混合的印的聚合物的相对选择系数也是计算的。比作非印的聚合物(捏)，IIP为Cd(II)有更高的选择。IIP被使用一个简单的批抽取过程从水样品为镉抽取用作吸着剂。从IIP的Cd2+抽取和它的恢复上的不同参数的效果被使用试验性的设计方法论评估并且优化。优化吸附/解吸附作用过程被申请从真实的水样品的镉移动。获得的恢复证明这IIP能从水样品被用于踪迹镉离子的移动。

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简介：LigandeffectofthecatalyticsystemWCl6-Et2AlClforringopeningmetathesispolymerization(ROMP)ofdicyclopentadiene(DCPD)wasinvestigated.Theexperimentalresultsshowthataddingstericallyhinderedphenol-2.6-di-tert-butylcresylol(DTBC)inthecatalyticsystemnotonlycanobviouslyincreasethemonomerconversionofpolymerizationbutalsoimprovethemechanicalproperties,suchasnotchedimpactstrength(NIS),tensilestrength(TS)ect.,ofthesynthesizedpolydicyclopentadiene(PDCPD),Asimilareffectcanbeobservedbyusingastericallyhinderdpolymericphenol-linearphenolformaldehyderesin(LPF)asaligand.

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简介：Cobaltandnickelcomplexes(1a-1dand2a-2d,respectively)supportedby2-imidate-pyridineligandsweresynthesizedandusedfor1,3-butadienepolymerization.ThecomplexeswerecharacterizedbyIRandelementanalysis,andcomplex1awasfurthercharacterizedbysingle-crystalX-raydiffraction.Thesolidstatestructureofcomplex1adisplayedadistortedtetrahedralgeometry.Uponactivationwithethylaluminumsesquichloride(EASC),allthecomplexesshowedhighactivitiestoward1,3-butadienepolymerization.Thecobaltcomplexesproducedpolymerswithhighcis-1,4contentsandhighmolecularweights,whilethenickelcomplexesdisplayedlowcis-1,4selectivityandtheresultingpolymershadlowmolecularweights.Thecatalyticactivitiesofthecomplexeshighlydependedontheligandstructure.Withtheincrementofpolymerizationtemperature,thecis-1,4contentandthemolecularweightoftheresultingpolymerdecreased.

简介：ThesorptionbehaviorofN-methyl-2-thio-imidazoleresin(MTIR)forRh(Ⅲ）wasinvestigated.TheoptmumsorptionconditionofMTIRforRh(Ⅲ）,sorptionratet1/2=84min,sorptioncapacity1.37mmolRh(Ⅲ）/gMTIR,[140.5mgRh(Ⅲ）/gMTIR],sorptionmolarratio0.34Rh(Ⅲ）/functionalgroup,distributioncoefficientD=2.5×10^3mg·g^-1weredetermined.ThesorptionselectivityofMTIRforRh(Ⅲ）inthepresenceofcommonmetalions,Fe^3+,Co^2+,Ni^2+andCu^2+wasexamined.Rh(Ⅲ）adsorbedonMTIRcanbeelutedquantitativelybyusingamixedsolutioncomposedof20%thio-urea-acetone:6molHCl.dm^-3(1:1vol.)usedasaneluent.Rh(Ⅲ）canbeseparatedfromthemixtureofRh(Ⅲ）andFe^3+,Co^2+,Ni^2+,Cu^2+byusingD72resinandMTIRsuccessively.