共查询到20条相似文献,搜索用时 31 毫秒
1.
Polystyrene-b-polyisoprene-b-poly(methylmethacrylate) (PS-b-PI-b-PMMA) triblock copolymer was synthesized by sequential anionic polymerization. The as-synthesized triblock copolymer contains side products of inadvertently terminated PS and PS-b-PI precursors. The side products can be effectively removed by semi-prep scale liquid chromatography using multiple injection method to obtain pure PS-b-PI-b-PMMA. It was found that the removed side product contains another polymer species, coupled PS-b-PI, which could not be recognized by size exclusion chromatography (SEC) analysis since the elution peak of the coupled product overlaps with that of PS-b-PI-b-PMMA. This study demonstrates that the size based separation of SEC is often not good enough to characterize complex polymers precisely and interaction chromatography can render unique advantage over SEC analysis. 相似文献
2.
Haritz Etxeberria Iñaki Zalakain Iñaki Mondragon Arantxa Eceiza Galder Kortaberria 《Colloid and polymer science》2013,291(8):1881-1886
Continuing with our previous work, in which CdSe nanoparticles were functionalized with polystyrene (PS) brushes (CdSe-PS) by the grafting through method, nanocomposites were prepared by adding them to a poly(styrene-b-butadiene-b-styrene) (SBS) triblock copolymer. After characterizing CdSe-PS nanoparticles obtained at different polymerization times of 3, 5, and 8 h by means of thermogravimetric analysis and gel permeation chromatography, CdSe-PS nanoparticles obtained after 5 h of polymerization (CdSe-PS(5h)) were chosen as the most adequate for the generation of nanocomposites. Atomic force microscopy (AFM) was used for morphological characterization of SBS/CdSe-PS(5h) nanocomposites. AFM images showed a good dispersion of the nanoparticles in the block copolymer, with the placement of the nanoparticles in the PS domains due to the improved affinity obtained by their functionalization with PS brushes. 相似文献
3.
Junfeng Zhou Xiaochen Dong Qiang Yang Jianjun Wang Haojie Yu Xu Chen 《European Polymer Journal》2007,43(5):1736-1743
A novel brush-type amphiphilic copolymer of PSMA-b-PTMSPMA was synthesized via ATRP technique. As-synthesized polymer was characterized by GPC and 1H NMR. It was of interest that the resultant polymer could self-assemble into micelles with different morphologies and sizes in selective solvents by adjusting the copolymer concentrations. These aggregates could be prepared into novel stable organic/inorganic hybrid nanomaterials by the gelation process. The size and structure of these aggregates and the corresponding hybrid nanomaterials were observed by TEM. 相似文献
4.
The triblock copolymers, poly(styrene-b-isoprene-b-ε-caprolactone)s (PS-b-PI-b-PCL) have been synthesized successfully by combination of anionic polymerization and ring-opening polymerization. Diblock copolymer capped with hydroxyl group, PS-b-PI-OH was synthesized by sequential anionic polymerization of styrene and isoprene and following end-capping reaction of EO, and then it was used as macro initiator in the ring-opening polymerization of CL. The results of DSC and WAXD show big effect of amorphous PS-b-PI on the thermal behaviors of PCL block in the triblock copolymers and the lower degree of crystalline in the triblock copolymer with higher molecular weight of PS-b-PI was observed. The real-time observation on the polarized optical microscopy shows the spherulite growth rates of PCL27, PCL328 and PS-b-PI-b-PCL344 are 0.71, 0.46 and 0.07 μm s−1, respectively. The atomic force microscopy (AFM) images of the PS90-b-PI66-b-PCL28 show the columns morphology formed by it’s self-assembling. 相似文献
5.
Yu Wang Guangdong Zhu Shun Wang Jianjun Xie Zhan Chen Ying Shi 《Molecules (Basel, Switzerland)》2021,26(19)
Poly(methyl acrylate)-b-poly(N-vinyl pyrrolidone/maleic anhydride/styrene) (PMA-b-P (NVP/MAH/St)) quaternary amphiphilic block copolymer prepared by reversible addition-fragmentation chain transfer (RAFT) was used to improve the anti-hydrolysis and dispersion properties of aluminum nitride (AIN) powders that were modified by copolymers. Its structure was characterized by Fourier transform infrared spectroscopy (FT-IR) and Hydrogen nuclear magnetic spectroscopy (1H-NMR). The results demonstrate that the molecular weight distribution of the quaternary amphiphilic block copolymers is 1.35–1.60, which is characteristic of controlled molecular weight and narrow molecular weight distribution. Through charge transfer complexes, NVP/MAH/St produces a regular alternating arrangement structure. After being treated with micro-crosslinking, AlN powder modified by copolymer PMA-b-P(NVP/MAH/St) exhibits outstanding resistance to hydrolysis and can be stabilized in hot water at 50 °C for more than 14 h, and the agglomeration of powder particles was improved remarkably. 相似文献
6.
Hojjat Toiserkani 《高分子科学》2016,34(3):288-297
In the present investigation, novel poly(amid-imide)/zinc oxide nanocomposites (PAI/ZnO NCs) containing benzoxazole and benzimidazole pendent groups with different amounts of modified zinc oxide nanoparticles (ZnO NPs) were successfully prepared via the ex situ method. Poly(amid-imide) (PAI) was prepared by direct polycondensation of 2-[3,5- bis(N-trimellitimidoyl)phenyl]benzoxazole (DCA) with 5-(2-benzimidazole)-1,3-phenylenediamine (DAMI) and provided the polymeric matrix with well-designed groups. The surface of ZnO NPs was functionalized with 3-aminopropyltriethoxysilane (APS) coupling agent to have a better dispersion and enhancing possible interactions of NPs with functional groups of polymer matrix. The amount of APS bonded to the ZnO surface was determined by thermogravimetric analysis. PAI/ZnO nanocomposites were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM). SEM analysis showed that the modified ZnO nanoparticles were homogeneously dispersed in polymer matrix. In addition, TGA data indicated an enhancement of thermal stability of the nanocomposite compared with the neat polymer. 相似文献
7.
Synthesis and characterization of Fe(II)-coordinated PS-b-P[NIPAM-co-(VBC-Fe-DMAP)] block copolymers
In this work,a new type of block polymers,polystyrene-b-poly[(N-isopropyl acrylamide)-co-(vinyl benzyl chloride)](PS-b-P(NIPAM-co-VBC)),was prepared via reversible addition fragmentation transfer polymerization,then pentacyano(4-(dimethylamino pyridine))ferrate(Fe-DMAP) was attached to VBC units through a quaternization process.The Fe(Ⅱ)-coordinated PS-b-P[NIPAM-co-(VBC-Fe-DMAP)]block copolymers were characterized by ~1H-NMR,FT-IR and TGA.The self-assembly behavior of the block copolymers was also investigated and the micelle morphology was characterized by TEM.It was found that the PS-b-P(NIPAM-co-VBC) block polymer and Fe-coordinated block copolymer could both form spherical micelles in DMF/MeOH mixed solvent. 相似文献
8.
Di Hu 《European Polymer Journal》2009,45(12):3326-5707
Polystyrene-block-poly(ethylene oxide) alternating multiblock copolymer (PS-alt-PEO) was synthesized with the combination of atom transfer radical polymerization (ATRP) and Huisgen 1,3-dipolar cycloaddition (i.e., click chemistry). The copolymer has been characterized by means of Fourier transform infrared spectroscopy (FTIR), 1H nuclear magnetic resonance spectroscopy (NMR), gel permeation chromatography (GPC) and differential scanning calorimetry (DSC). The PS-alt-PEO alternating multiblock copolymer was incorporated into epoxy resin to investigate the behavior of reaction-induced microphase separation, which has been compared to the case of the thermosets containing PS-b-PEO diblock copolymer. The morphology of epoxy thermosets containing PS-alt-PEO alternating multiblock copolymer were investigated by means of atomic force microscopy (AFM), and small-angle X-ray scattering (SAXS) and the nanostructures were detected in all the thermosetting blends investigated. In marked contrast to the case of the thermosets containing PS-b-PEO diblock copolymer, the thermosets containing PS-alt-PEO multiblock copolymer displayed disordered nanostructures, which have been interpreted on the basis of the restriction of the alternating multiblock topology of the block on the formation of the nanostructures via reaction-induced microphase separation. 相似文献
9.
Nanofiltration membranes based on blend of polysulfone-g-poly(tert-butylacrylate) copolymer and polysulfone were prepared by phase inversion technique. ATRP grafting of tert-butylacrylate from chloromethylated polysulfone was used for the grafted polymer synthesis. The copolymer was characterized with FTIR, NMR, DSC and TGA. The prepared membranes were characterized in terms of pure water flux, water contact angle, cut off molecular weight, salt rejection and scanning electron microscopy. 相似文献
10.
《Colloids and surfaces. B, Biointerfaces》2010,80(2):452-459
Poly(vinylpyrrolidone-b-styrene) (PVP-b-PS) diblock copolymers tethered to glass surfaces were prepared, and the effects on protein adsorption and cellular behavior to the glass and the modified glass surfaces investigated. The PVP-b-PS grafting process was confirmed by water contact angle and XPS measurements. The results obtained for the water contact angles suggest that there are two phases that coexist on the PVP-b-PS block copolymer tethered surface, under aqueous conditions. Although the PVP-b-PS surface possessed, to some extent, a protein resistant property, following introduction of the PS segment to the end of tethered PVP, both fibrinogen and lysozyme adsorption were increased significantly. The PVP-b-PS modified surface, based on Western-blot analysis, appeared to have the greatest amount of surface bound vitronectin, however the conformation of the adsorbed vitronectin may have subsequently been affected by the surface tethered copolymer as was suggested by cell culture results. From these results, we proposed that protein adsorption and cell adhesion can be regulated by tuning the chemical compositions of diblock copolymers tethered to surfaces. 相似文献
11.
Gold nanoparticles by using the mixture of polystyrene-block-poly(2-vinyl pyridine)/poly(2-vinyl pyridine)-block-poly(ethylene oxide) (PS-b-P2VP/P2VP-b-PEO) block copolymers as encapsulating agent was prepared. The prepared nanoparticles were characterized by transmission electron microscopy, UV-Vis spectroscopy and contact angle. It is demonstrated that the obtained gold nanoparticles are covered with mixed block copolymer shells. The hydrophilic property of the nanoparticles can be varied by the change of the dispersion medium. The obtained gold nanoparticles with mixed block copolymer shells are stable in organic solvents (such as tetrahydrofuran and toluene) and water. 相似文献
12.
Silica nanoparticles (NSiO2) are modified with mixed polymer brushes derived from a block copolymer precursor, poly(methyl methacrylate)-b-poly(glycidyl methacrylate)-b-poly(tert-butyl methacrylate) with short middle segment of PGMA, through one step ??grafting-onto?? approach. The block polymer precursors are prepared via reversible addition?Cfragmentation chain transfer-based polymerization of methyl methacrylate, glycidyl methacrylate, and tert-butyl methacrylate. The grafting is achieved by the reaction of epoxy group in short PGMA segment with silanol functionality of silica. After hydrolysis of poly(tert-butyl methacrylate) segment, amphiphilic NSiO2 with ??V-shaped?? polymer brushes possessing exact 1:1 molar ratio of different arms were prepared. The functionalized particles self-assemble at oil/water interfaces to form stable large droplets with average diameter ranging from 0.15?±?0.06 to 2.6?±?0.75?mm. The amphiphilicity of the particles can be finely tuned by changing the relative lengths of poly(methyl methacrylate) and poly(methacrylic acid) segments, resulting in different assembly behavior. The method may serve as a general way to control the surface property of the particles. 相似文献
13.
通过原位聚合法制备了本质阻燃聚苯乙烯[P(St-co-AEPPA)]/有机改性蒙脱土(OMMT)纳米复合物[P(St-co-AEPPA)/OMMT], 并用普通聚苯乙烯/有机改性蒙脱土(PS/OMMT)复合物作为对比实验, 研究了含磷、氮单体丙烯酸羟乙基-苯氧基-二乙基磷酰胺(AEPPA)和OMMT等添加物对本质阻燃聚苯乙烯性能的影响.用X射线衍射仪(XRD)和透射电子显微镜(TEM)分析了复合材料的结构与形貌, 并对OMMT在基体中的分散机理进行了讨论.用差示扫描量热仪(DSC)、热重分析(TGA)和微型量热仪(MCC)研究了材料的热性能和燃烧性能.结果表明, AEPPA和OMMT能够显著提高基体的热稳定性和阻燃性. 相似文献
14.
Donghyun Cho Taihyun Chang Apostolos Avgeropoulos Nikos Hadjichristidis 《European Polymer Journal》2003,39(11):2155-2160
Temperature gradient interaction chromatography (TGIC) was applied for the separation of a complex miktoarm star copolymer which has one polystyrene (PS) arm and three polystyrene-b-polyisoprene (PS-b-PI) diblock copolymer arms. Such miktoarm star polymers are much more difficult to characterize than branched homopolymers since the byproduct, typically polymers with missing arm(s) or coupled products, have not only different molecular weights but also different compositions. TGIC was able to fully separate the byproducts, and the composition of the molecular species corresponding to the different separated elution peaks was determined by two methods, fractionation/NMR and multiple detection (UV and RI). A reasonable agreement between the results of the two methods was obtained. By using the composition found, the corresponding molecular weights were determined by multi-angle light scattering detection. Based on the composition and the molecular weight we were able to identify the structure of the different molecular species. 相似文献
15.
A trace amount of solvents such as n-octane, n-nonane, n-decane, ethyl acetate, n-propyl acetate, isoamyl acetate, toluene, ethyl benzene, n-propyl benzene, isopropyl benzene and chloro benzene was passed through the column of a gas chromatograph of which the stationary phase is poly(tert-butyl acrylate-b-methyl methacrylate), poly(tBA-b-MMA), block copolymer with low polydispersity, prepared via ATRP of tBA and MMA, respectively. The retention diagrams to determine the thermal transition of the polymer were obtained by plotting the logarithm of the specific retention volumes of isoamyl acetate and toluene against reciprocal values of absolute column temperatures between 40 and 170 °C by inverse gas chromatography (IGC) technique. Three glass transition temperatures, Tgs of poly(tBA-b-MMA) were determined at 50, 70 and 105 °C by IGC indicating the phase separation of the polymeric blocks in the copolymer. The thermodynamical interaction parameters such as weight fraction activity coefficient of solvent at infinite dilution, , Flory-Huggins polymer-solvent interaction parameter, , equation-of-state polymer solvent interaction parameter, , effective exchange energy parameter, Xeff, and solubility parameter of the copolymer, δ2 were calculated at studied temperatures. The closeness of parameters of the poly(tBA-b-MMA) to those of the PMMA indicated that the continuous phase is MMA block in the microphase separated block copolymer. It seems that IGC is a reliable technique to study a phase separated block copolymer which contains nanosized domains. 相似文献
16.
New polymer nanocomposites containing iron oxide nanoparticles stabilized with a biocompatible copolymer of 1-vinyl-1,2,4-triazole with N-vinylpyrrolidone were produced. The synthesis was conducted using the method of chemical reduction of iron ions with hydrazine hydrate in an aqueous medium in the presence of a polymer matrix. The ESR spectroscopy data showed that the core—shell type nanoparticles were obtained. The core generally consistsed of zero-valence iron coated with an oxide shell. According to the data of transmission electron microscopy, the obtained polymer nanocomposites consisted of nanoparticles of mainly spherical shape with a diameter from 1 to 14 nm. Aggregates formed from individual stabilized nanoparticles of up to 75 nm in size (in most cases) were also observed. These aggregated particles were found to self-organize and form branched chains. Nanocomposites were characterized by a different particle-size distribution, which was determined by the initial ratio of the copolymer and the precursor of iron nanoparticles. 相似文献
17.
N. P. Kuznetsova T. G. Ermakova A. S. Pozdnyakov A. I. Emel’yanov G. F. Prozorova 《Russian Chemical Bulletin》2013,62(11):2509-2513
Novel organic-inorganic nanocomposites were synthesized by chemical reduction of silver ions from silver acetate in DMSO and DMF solutions in the presence of the stabilizing copolymer of 1-vinyl-1,2,4-triazole-acrylonitrile. The solvents DMSO and DMF can act as efficient reducing agents for silver ions, which makes it possible to carry out the reaction under mild conditions and simplify procedures of nanocomposite isolation. The structure and properties of the starting copolymer and related nanocomposites were characterized by UV, IR, and 1H and 13C NMR spectroscopy, as well as transmission electron microscopy and thermogravimetry. The prepared polymer nanocomposites contain 6.8–7.2% silver in the form of nanoparticles with a size of 2–20 nm uniformly dispersed in the polymer matrix. The nanocomposites are readily soluble in DMSO and DMF and do not decompose on heating to 260 °C. 相似文献
18.
聚苯乙烯/蒙脱土纳米复合材料的制备及结构研究 总被引:4,自引:1,他引:4
以可与苯乙烯发生共聚的阳离子表面活性剂乙烯苄基二甲基十八烷基氯化铵(VOAC)为插层处理剂改性蒙脱土(VC18-MMT),有机蒙脱土在超声波强剪切作用以及乳化剂作用下预分散在乳化剂溶液中,然后引入苯乙烯单体进行原位乳液聚合制备聚苯乙烯/蒙脱土纳米复合材料.采用XRD和TEM对纳米复合材料的结构进行了表征.结果表明,绝大多数的蒙脱土被剥离成单个片层均匀的分散在聚合物基体中;动态力学分析表明,纳米复合材料的储能模量和玻璃化温度均有所增加,而动态损耗有所降低;接枝在蒙脱土片层上的聚合物通过与锂离子进行阳离子交换反应提取下来,采用GPC和NMR对接枝聚合物的结构进行了表征,结果表明,接枝聚合物是较基体分子量低且分布很宽的苯乙烯和乙烯苄基二甲基十八烷基氯化铵的共聚物,计算表明每一个共聚物分子链上平均含有大约25个乙烯苄基二甲基十八烷基氯化铵分子. 相似文献
19.
Bishnu Prasad Bastakoti Sudhina Guragain Yuuichi Yokoyama Shin-ichi Yusa Kenichi Nakashima 《Colloid and polymer science》2010,288(9):991-996
Organic–inorganic nanohybrid particles are prepared in aqueous solution from poly(ethylene oxide-b-sodium 2-acrylamido-1-propanesulfonate-b-styrene) (PEO-b-PAMPS-b-PS) triblock copolymer and ferric ions. The hybrid micelles were characterized by dynamic light scattering, scanning electron
microscopy, transmission electron microscopy, and zeta-potential measurements. The hydrodynamic diameter of the hybrid micelles
ranges from 68 to 118 nm depending on the concentration of the polymer and the amount of ferric ions loaded on the polymer.
Zeta-potential measurements revealed that the micelles are assembled mainly by electrostatic interaction between the ferric
ions and the negatively charged PAMPS block in the PEO-b-PAMPS-b-PS. 相似文献
20.
The production of exfoliated polymer/clay based nanocomposites is crucial to obtain an actual benefit of nanoscale reinforcement in the polymer matrix. In this project, the production of exfoliated polymer/clay nanocomposite was aimed through the use of poly(ethylene-co-vinyl acetate) (EVA) copolymer as matrix and organically modified montmorillonite (O-MMT) as nanofiller. The research work involved the use of pre-swelled technique through magnetic stirring and ultra-sonication to obtain more readily exfoliated and dispersed O-MMT nanofiller for EVA nanocomposite production. The aims were to allow the improvement in O-MMT exfoliation and dispersion when the nanofiller was incorporated in high loading (greater than 3 wt%) into the copolymer. The original and pre-swelled O-MMTs were employed to produce the EVA/O-MMT nanocomposites with 1, 3, 5, 7 and 9 wt% nanofiller by melt compounding technique. The results of TEM, tensile and fatigue tests, XRD, FTIR and DMA proved that the pre-swelling technique applied on the O-MMT before melt compounding with the EVA copolymer can bring positive impact to the performance of the nanocomposite. As opposed to the original O-MMT, the pre-swelled O-MMT has the ability to improve the tensile toughness, cyclic stability and storage modulus of the EVA copolymer even when high O-MMT loading (7 wt %) was employed. Improvement in the EVA - O-MMT interactions in the nanocomposite system was postulated to be the main reason for such observations. 相似文献