简介：The1,1'-binaphtholbasedoligomers3and7with3,3'-acetylene-phenylene-acetylenespacerwerepreparedfromBINOL1.ThehighopticalrotationvalueandCDspectrademonstratedthemainchainchiralityoftheoligomermolecule.TheUV-VISandfluorescentspectraevidencethecharacteristicsofconjugatedstructure.Incomparisonwitholigomer2bearing3,3'-acetylenespacer,theoligomers3and7havelongerefficientconjugationsegment,andtheirfluorescentquantumyields(φ)increased(0.60-0.65versus0.14).Extendingtheeffectiveconjugationsegmentwouldimprovethephotophysicalpropertiesofchiralconjugatedpolymers.``

简介：Poly（β-carboxyethylmethylsiloxane）-LiClO4andpoly（β-alkoxylethylmethylsiloxane）-LiClO4crosslinkedfllmshavebeenprepared.Theionicconductivityofthefilmsdependsonthepolymerspecies,concentrationoflithiumperchlorate,temperatureandcontentofcrosslinkingagent.Theeffectofhighpolarorganicsolvent1,4-butyrolactoneontheionicconductivityandmechanicalpropertiesofpoly（β-carhoxyethylmethylsiloxane）-LiClO4systemwasalsoinvestignied.

简介：Ionicconductivityvaluesforsegmentedpolyetherpolyurethaneurea（PEUU）complexeswithLiClO4weredeterminedandvaluesashighas～1.1×10-4S·cm-1at353Kand～1.0×10-5S·cm-1at306Kwereachieved.TheionicconductivitydatawereanalyzedusingtheVTF（Vogel-Tamman-Fulcher）equationandWLF（Williams-Landel-Ferry）typeequation.Valueshavebeenestimatedforthe"apparent"activationenergiesofiontransportfromVTFequationandtheylieintherange2.70—5.53kJ·mol-1.

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简介：开车的听氧协作自己组装在包含organotin的块共聚物被开发，它被激进的增加部分转移(木排)准备方法并且由胶化浸透层析(GPC)并且<描绘了啜class=“a-plus-plus”>1H-NMR。并且有在在CHCl的不同集中的各种各样的链长度比率的这些块共聚物的self-assemblies<潜水艇class=“a-plus-plus”>3根据DLS和TEM的结果是稳定的。另外，它也在规定上被给卓见调查由补充说dibutyltin二氯化物和可能的机制被建议的块共聚物自己组装。

简介：Blendsofpoly(3-hydroxybutyrate-co-3-hydroxyhexanoate)(PHBHHx)andpoly(butylenesuccinate-adipate)(PBSA),bothbiodegradablesemicrystallinepolyesters,werepreparedwiththeratioofPHBHHx/PBSArangingfrom80/20to20/80bymeltmixingmethod.Differentialscanningcalorimetry(DSC),thermogravimetryanalysis(TGA),dynamicmechanicalthermalanalysis(DMA),polarizingopticalmicroscopy(POM)andwideangleX-raydiffractometer(WAXD)wereusedtostudythemiscibilityandcrystallizationbehaviorofPHBHHx/PBSAblends.ExperimentalresultsindicatethatPHBHHxisimmisciblewithPBSAasshownbythealmostunchangedglasstransitiontemperatureandthebiphasicmelt.

简介：Inthispaper,thetwoeffluentsfromPBA(3-phenoxy-benzaldehyde)productionprocessweretreatedbypolymericadsorbentCHA-111.PBAorPBC(3-phenoxy-benzoicacid)wasrecoveredfromthewastewaterintheprocessofneutralization.Asasecondarytreatmentmethod,adsorptionwithCHA-111showedbetterefficiencythanphotocatolyticdecompositionandsolventextraction.Theoptimaltechnologicalparameterswere:adsorption:currentvelocity:2.0BV/hr(bedvolumeperhour),roomtemperature;desorption:currentvelocity:2.0BV/hr(bedvolumeperhour),roomtemperature;desorption:currentvelocity:1.0BV/hr,80℃,8%sodiumhydroxideaqueoussolutions.Inconclusion,99.9%CODintheneutralizingwastewaterand98.4%CODinthehydrolysiswastewaterareremovedsuccessfully.

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

简介：Thispaperintroducesanimprovednewmethodwhichisusedtorecoversilverassilvernitratebyionexchangefromthewasters.Inthismethod,wecanrecoversilvernitrate,onlybyusingakindofionexchangeresinandtwoionexchangeprocesses.Itcanreplacetheoriginalrecoverymethodinwhichtwokindsofionexchangeresinsandthreeionexchangeprocessesareneeded.Theresultissatisfied

简介：FirstCircular/Pre-registration(e-mailedition)July14-18,2003KanazawaInstituteofTechnology,Nonoichi,IshikawaPref.,JAPANOrganizedbyJapanAssociationofIonExchange(JAIE)INVITATIONOnbehalfoftheJapanAssociationofIonExchange(JAIE),the3rdInternationalConferenceonIon

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简介：Thiscontributionreportsethylenepolymerizationbehavioroftitaniumcomplexesincorporatingbis(phenoxyimine)ligands.Sixphenoxy-imineTi(IV)complexes{6-R1-2-[CH=N(2,6-difluoro-3,5-diR2-4-R3Ph)]C6H3O}2TiCl2(1:R1=H,R2=H,R3=H;2:R1=H,R2=H,R3=4-vinylphenyl;3:R1=CH3,R2=H,R3=H;4:R1=CH3,R2=H,R3=4-vinylphenyl;5:R1=CH3,R2=F,R3=H;6:R1=CH3,R2=F,R3=4-vinylphenyl)havebeensynthesizedandevaluatedforethylenepolymerizationusingdriedMAO(simplifiedasDMAO)ascocatalyst.AnobviouscatalyticheterogeneityofCat2(Complex2/DMAO)towardsethylenepolymerizationwasobserved,whichwasillustratedbydecreasedactivity,multimodalmolecularweightdistributionandpartiallyimprovedparticlemorphologycomparingwithCat1.Moreover,Cat3exhibits'living'characteristicsintheprocessundercertainconditions(25°C,lessthan20min).Otherwise,themoderatetohighethylenepolymerizationactivityofca.105-106gPE/(molTi·h)andhighmolecularweight(Mw=105-106)ofpolyethylenecanbeobtainedbychangingtheskeletonstructureofthesecomplexes.

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

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

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：TheconductivitybehaviorofAl(OH)3-acrylamidehybridpolyacrylamide(hybridPAAm)indistilledwaterwasstudied.Adiscontinuityphenomenonoftheconductivity(k)versusconcentration(c)curveofthehybridPAAminacertainconcentrationregimeisfound.ThisphenomenonisdependentonthemolecularweightofthehybridPAAmandontheparticlesizeandcontentoftheAl(OH)3colloidinthehybridPAAm.ThisphenomenonwasaccountedforassumingionizationofthehybridPAAm.

简介：TheeffectsofHDPEmatrixtoughnessonthebrittle-ductiletransitionofHDPE/CaCO3blendsareinvestigated.NotallHDPEcanbetoughenedbyCaCO3particles.TheabilityofthematrixtoyieldplaysafundamentalroleindetermingwhetherHDPEcanbetoughenedornot.Thereexistsacriticalmatrixtoughness(Isc≈45J/m)belowwhichHDPEcannotbetoughenedobservablybyCaCO3particleatgivenaveragesize,andabovewhichthecriticalmatrixligamentthickness（τ?）isproportionaltomatriximpactstrength.

简介：Thechemicalgraftingofthiolterminatedpoly（sodiumstyrenesulfonate）（HS-PSSS）chainsfromsodiumnitrate（NaNO3）saltsolutiontoagoldsurfacewasinvestigatedwithaquartzcrystalmicrobalancewithdissipationmonitoring（QCM-D）indifferentsaltconcentrations.ItwasfoundthatatlowsaltconcentrationgraftingdensityofHS-PSSSwaslowandthegraftedchainsadoptedamushroomconformation.Withtheincreaseofsaltconcentrationpolyelectrolytechainsunderwentatransitiontowardcoiledstateduetoreductionofelectrostaticrepulsionandasaresultmorechainsweregraftedonthesurface.WhenthegraftingdensityreachedacertainlimitafterwhichfurthergraftingcausedrepulsionbetweenalreadygraftedHS-PSSSchainsandasaresultgraftedchainsadoptedabrushconformation.