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

简介：Inthisstudy,apoly(etherblockamide)(Pebax1657)compositemembraneappliedforCO2capturewaspreparedbycoatingPebax1657solutiononpolyacrylonitrile(PAN)ultrafiltrationmembrane.Ethanol/watermixturewasusedasthesolventofPebaxandtheeffectsofethanol/watermassratiosandPebaxconcentrationonthepermeationpropertiesofcompositemembranewerestudied.Toenhancethecompositemembranepermeance,thegutterlayer,madefromreactiveaminosiliconecrosslinkingwithpolydimethylsiloxane(PDMS),wasdesigned.Theinfluenceofcrosslinkingdegreeofthegutterlayeronmembraneperformancewasinvestigated.Asaresult,aPebax/aminoPDMS/PANmultilayermembranewithhexaneresistancewasdeveloped,showingCO2permeanceof350GPUandCO2/N2selectivityover50.Theblendofpolyethyleneglycoldimethylether(PEG-DME)withPebaxascoatingmaterialwasstudiedtofurtherimprovethemembraneperformance.AfterbeingcombinedwithPEG-DMEadditive,CO2permeanceofthefinalPebax-PEG-DME/amino-PDMS/PANcompositemembranereached400GPUabovewithCO2/N2selectivityover65.

简介：WithN-vinyl-2-pyrrolidone(NVP)anditaconicacid(IA),poly(N-vinyl-2-pyrrolidone/itaconicacid)[P(NVP/IA)]hydrogelwassynthesizedbyfreeradicalsolutionpolymerization.ThestructureofthisP(NVP/IA)wascharacterizedbyIR.Effectsofconcentrationofitaconicacid,amountofcross-linkagent,N,N′-methylene-bis-acrylamide,reactiontemperature,andtimeonpropertiesofswellingratio(SR)ofthehydrogelwereinvestigated.Theresultsshowthatthebestswellingpropertyofthehydrogelisobtainedat50℃and1.5h.pHsensitivityincreasesastheconcentrationofitaconicacidinthehydrogelsystemincreases.Swellingratioofthehydrogeldecreasesastheamountofcross-linkagentincreases.

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简介：Underdifferentreactionconditions,theexpectedandunexpectedreactionproducts(ofwhichX-raycrystallographicstructurewaspresented)ofetherificationof2-per(poly)fluoroethyl4-substitutedphenolwithβ-haloethanolcanbeobtainedrespectively.

简介：阶段PVDF水晶结构和在先存在的阶段PVDF球粒以内的豌豆的结晶化上的豌豆的效果被光显微镜学OM，红外线的光谱学红外和扫描电子显微镜学SEM调查了。结果证明阶段PVDF球粒由展出高度弄弯的像滚动的形态学的lamellae组成并且在充满豌豆的混合优先地发展。与增加豌豆集中，滚动直径增加和滚动更好与对方被分开。豌豆在interspherulitic区域使第一结晶，transcrystalline层发展。随后，豌豆的transcrystalline层继续在阶段PVDF球粒以内成长，例如在在滚动之间的区域，直到在另外的豌豆transcrystalline层或球粒上侵犯。结晶化动力学结果显示在阶段PVDF的intraspherulitic区域的豌豆晶体的生长率与阶段PVDF的结晶化温度与豌豆，而是否定豌豆的内容显示出积极关联。

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

简介：PVDF的词法特征上的PBS的效果被光、原子的力量显微镜学在各种各样的条件下面调查了。整洁的PVDF在170戠?与非常地弱的birefringence形成大表格球粒，这被发现?M

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：Ithasbeenwellknownthatfluorinatedpolyurethanesexhibituniquelylowsurfaceenergy,biocompatibilityandbiostability,thermalandoxidativestabilityandnonstickingbehavior.Consequently,thesepolymershaveattractedconsiderableinterest.However,themechanicalpropertiesoffluorinatedpolyurethanesusuallydeclinewithincreasingfluorinecontents.Theblendingoffluorinatedpolyurethaneswithnormalpolyurethanewascarriedouttoachievebalancedmechanicalandsurfaceproperties.Itwasfoundthatpolyurethanewithgoodmechanicalpropertiesandlowsurfaceenergycanbeobtainedbyaddingasmallamountoffluorinatedpolyurethane.Thefluorinatedsidechainscaneasilymigratetouppermostsurfacesoftheblendsuntillthefluorinelevelatthesurfacebecomesalmostsaturated.Ithasbeenshownfromcontactangle,XPSandAFMmeasurementsthatonlyaslittleas0.34wt%offluorinelevelisenoughtoproduceasurfacesaturatedwithfluorine,andthefluorinelevelattheuppermostsurfaceisonehundredtimeshigherthanthatintheblendbulk.Thefinaloutersurfacestructuresofthepolyurethaneblendwereindependentofthecontentofthefluorinatedpolyurethaneintheblendsduetothesurfacessaturatedbyfluorine.

简介：Carbonylationofallylhalidescatalyzedbypoly(N-vinyl-2-pyrro-lidone)anchoredpalladiumcatalystaffordsβ,r-butonicacidunderatmo-sphericpressureandatroomtemperature.Theactivityandefficiencyofthecatalystaremuchhigherthanthoseofthereportedcatalystsforthisreaction.

简介：Anovelsmallband-gapconjugatedpolymer-poly[(3-acetylpyrrole-2,5-diyl)(4-dimethylaminobenzyliene)(3-aeetylpyrrolequinodimethane-2,5-diyl)](PAPDMABE)-anditsprecursorweresynthesizedbyasimplemethodandcharacterizedby1H-NMR,FT-IR,TGAandUV-VIS.ThepolymercanbedissolvedinstrongpolarsolventssuchasDMSO,DMForNMP.Theband-gapenergyofPAPDMABEwasfoundtobe0.95eV.Theconductivityofdopedproductswithiodinefallsintherangeofasemiconductor.``

简介：3-Ethynyl-4-（trimethylsilyl）thiophene（1a）and3-ethynyl-4-bromothiophene（1b）selectivelyundergoacetylenepolymerizationsinthepresenceoftheMoCl5-andWCl6-Ph3SiHcatalyststogivesoluble,high-molecular-weightpoly（thienylacetylenes）（2）（Mwupto602000）inhighyields（upto100%）.LighttransmissionspectraofTHFsolutionsof2continuouslyred-shiftwithincreasingconcentration.Theconcentratochromismshowsalogarithmicconcentrationdependence;thatis,theopticaltransitionsof2arepredictablytunablebysimplychangingtheirconcentrations.

简介：Poly(4-vinylpyridine)(P4-VP)nanofiberandfluoresentpoly(4-vinylpyridine)/porphyrin(P4-VP/TPPA)nanofiberwererespectivelypreparedbyelectrospinning.TheeffectoftheconcentrationofP4-VP/dimethylformamide(DMF)electrospinningsolutionsonthemorphologyofP4-VPnanofiberwasinvestigatedanditwasfoundthattheaveragediameterofthenanofiberofP4-VP/DMFincreasedwiththeincreaseoftheconcentrationofthespinningsolution.AftertheadditionofTPPAtotheP4-VP/DMFspinningsolution,thediameterofP4-VP/TPPAnanofiberbecameevenduetotheincreaseoftheconductivityoftheP4-VP/DMF-TPPAsolution.Thephotoluminescent(PL)spectralanalysisindicatesthattheemissionpeakpositionofP4-VP/TPPAnanofiberisalmostthesameasthatofpureTPPAatabout650nmwithoutpeakshift,andwhenitwasstoredfor20days,theemissionpeakofP4-VP/TPPAnanofiberisalsoat650nm,indicatingthatthefluorescentpropertyofP4-VP/TPPAnanofiberisstable.Fourier-transforminfrared(FTIR)spectrumconfirmsthechemicalcompositionoftheresultingP4-VP/TPPAcompositenanofiber.

简介：Aseriesofpoly(2-acetoxyethylmethacrylate)/polystyrene(PAEMA/PS)latexinterpenetratingpolymernetworks(LIPNs)werepreparedbyseededsoap-freeemulsionpolymerizationofstyreneonthecrosslinkedPAEMAseedparticlesusinganoil-solubleinitiator.ThesePAEMA/PSLIPNsshowedawell-definedphase-separatedstructurewithPSphasedispersingincontinuousPAEMAphase.ThedomainsizeofPSphasewasfoundtodependonthecrosslinkingdegreeofPAEMAseedparticlesandtheamountofsecond-stagestyrenemonomer.

简介：:Twonovelpoly[(3-alkyhhiophene-2,5-diyl)-(benzylidenequinomethane-2,5-diyl)s]derivatives,poly[(3-butylthiophene-2,5-diyl)-(p-N,N-dimethylamino)benzylidenequinomethane-2,5-diyl)](PBTDMABQ)andpoly[-(3-octylthiophene2,5-diyl)-(p-N,N-dimethylamino)benzylidenequinomethane-2,5-diyl)](POTDMABQ),weresynthesized.Thebandgapsofthetwopolymersarecalculatedas1.75eVforPBTDMABQand1.69eVforPOTDMABQ,respectively.Thehomogenousfilmsofthetwopolymerswerepreparedandtheirthird-ordernonlinearopticalpropertieswerestudiedbythebackwarddegeneratefour-wavemixingat532nm.Byusingtherelativemeasurementtechnique,thethird-ordernonlinearopticalsusceptibilitiesofPBTDMABQandPOTDMABQarecalculatedas5.62×10^-9and1.22×10^-8ESU,respectively.Itisfoundthatsubstitutedalkygroupshavestrongeffectsonthebandgapandnonlinearopticalpropertiesofthetwopolymers.Therelativelybigthird-ordernonlinearopticalsusceptibilitiesandsmallbandgapofPOTDMABQresultedmainlyfromthelongeralkylwithstrongelectron-donatingabilitycanenhancethedelocationdegreeofconjugatedπelectronics.

简介：二氧化碳共聚物聚氨酯胺PUA与聚丙烯碳酸盐PPC被混合以便没有牺牲另外的机械性质，改进PPC的坚韧和灵活性。与纯PPC相比，有装载的5wt%PUA的PPC/PUA混合证明400%在裂缝在延伸增加，虽然相应让步力量象稍微显示出的33.5MPa和幼仔模量一样仍然保持高减少。在PPC/PUA的结合的相互作用混合的分子间的氢被FTIR，2D红外和XPS系列分析，和PUA的细微地驱散的微粒结构在PPC证实在SEM图象被观察，它为PPC的韧化的机制提供了好证据。

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简介：Bilayerhumidity-responsiveactuatorsaregenerallycomposedofactuatingandsupportinglayersofdifferentmaterialswithlargelydifferentwettability.Suchkindsofbilayeractuatorssufferfromlowadhesiveforcebetweenthetwolayersduringusage.Thisstudydemonstratesthepreparationofhumidity-responsivebilayeractuatorsthathavethesamematerialsintheactuatingandsupportinglayerstoavoidtheadhesiveissue.Thebilayeractuatorsconsistofaporouspoly(acrylicacid)σAA)/poly(allylaminehydrochloride)(PAH)layerandanonporousPAA/PAHlayerthatarefabricatedbyexponentiallylayer-by-layerassemblymethod.Atahigh/lowrelativehumidity(RH),thenonporousPAAIPAHlayercanefficientlyexpand/shrinkbyabsorbing/desorbingwaterwhilethevolumeexpansion/shrinkageoftheporousPAA/PAHlayerinanenvironmentwithchangedhumidityissignificantlysuppressedbythemicrometer-sizedpores.Thelargelydifferentexpansion/shrinkageofthenonporousandporousPAA/PAHlayerswhensubjectedtohumiditychangesenablesrapidandreversiblerolling/unrollingmotionsofthebilayeractuator.Thebilayeractuatorshowsafasterrollingspeedandalargerbendingcurvaturewhensubjectedtoalargerhumidityincrease.

简介：结晶化修正(vinylidene氟化物)(PVDF)poly为PVDF并且poly的混合电影(甲基methacrylate)(PMMA)被调查。集体crystallinity(c)并且进一步，阶段内容(PVDF的F())，与不同集体比率为asprepared混合电影被学习。另外，c和F的变化()一旦PMMA部件从相关混合系统被移开，系统地被探查。DSC，FTIR和XRD大小都显示了那1)c，F()并且甚至阶段的内容(F())与PMMA的增加减少了；2)与PMMA的抽取，c和F()当时，增加了F()减少。它是值得注意的c和F的增加()取决于提取PMMA(EPMMA)的相对数量，即，越多PMMA被移开，越多c和F()增加。这些结果从PMMA成分揭示阻碍者效果到PVDF的结晶化，并且因而，当PMMA被提取时，这限制将被释放。