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APPLICATION OF SURFACE GRAFTED POLY N-ISOPROPYL ACRYLAMIDE BY RADIATION TECHNOLOGY FOR PROTEIN SOLUTION CONCENTRATION
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作者 孙以实 李怀忠 +1 位作者 刘鹏飞 哈鸿飞 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 1991年第4期353-357,共5页
Poly N-isopropyl acrylamide (abbreviated as PNIPA) as a kind of thermally sensitive hydrogel is utilized to concentrate Bovin Serum Albumin (BSA) solution. In order to decrease its surface adsorption to BSA in aqueous... Poly N-isopropyl acrylamide (abbreviated as PNIPA) as a kind of thermally sensitive hydrogel is utilized to concentrate Bovin Serum Albumin (BSA) solution. In order to decrease its surface adsorption to BSA in aqueous solution, surface layer grafting of the gels by radiation technology was carried out. The results showed that hydroxyl propyl methacrylate (HPMA) grained gel exhibited a low level of BSA adsorption and still kept the original thermally sensitive properties of PNIPA hydrogels. 展开更多
关键词 poly n-isopropylacrylamide hydroxyl propyl methacrylate Boving serum albumin thermally sensitive hydrogel radiation surface grafting
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N⁃苯基马来酰亚胺共聚物的合成及对PVC树脂耐热改性效果研究
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作者 孙芳芳 宋运运 《中国塑料》 CAS CSCD 北大核心 2024年第7期49-54,共6页
通过种子乳液聚合结合半连续加料方式,成功聚合出分子结构一致且与聚氯乙烯(PVC)树脂具有良好相容性的聚(N‐苯基马来酰亚胺‐苯乙烯‐丙烯腈)(PNSA)共聚物胶乳,将其与PVC树脂直接复合制备PNSA/PVC复合材料,并对PNAS耐热改性的效果进行... 通过种子乳液聚合结合半连续加料方式,成功聚合出分子结构一致且与聚氯乙烯(PVC)树脂具有良好相容性的聚(N‐苯基马来酰亚胺‐苯乙烯‐丙烯腈)(PNSA)共聚物胶乳,将其与PVC树脂直接复合制备PNSA/PVC复合材料,并对PNAS耐热改性的效果进行评价。结果表明,PNSA纳米胶乳颗粒粒径在155.3~251.5 nm之间,粒径分布均一;PNSA共聚物分子组成呈无规结构,分子结构一致,差示扫描量热曲线呈现单一的玻璃化转变温度(T_(g)),且与PVC树脂具有极佳的相容性;PNSA含量由0升高至50%(质量比,下同)时,复合材料的T_(g)由84.8℃提高到107.2℃,提高了22.4℃,维卡软化温度由71.2℃提高到91.9℃,提高了20.7℃;除耐热性改善以外,复合材料的力学性能也有一定程度的提高,本文的研究有利于PVC应用领域的进一步拓展。 展开更多
关键词 聚氯乙烯 n‐苯基马来酰亚胺 自由基共聚 种子乳液 耐热改性
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偶氮苯基小分子光控聚N-异丙基丙烯酰胺在离子液体中的自组装
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作者 李佩琪 王彩虹 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2024年第2期32-38,共7页
偶氮苯基材料因其具有可逆的光致顺反异构特性,可调控聚合物的自组装行为而受到广泛关注。采用不同结构且广泛商业化的偶氮苯基小分子(偶氮苯(AZO)、对羟基偶氮苯(AZO-OH)、对氨基偶氮苯(AZO-NH2)、二甲基黄[AZO-N(CH_(3))_(2)])作为光... 偶氮苯基材料因其具有可逆的光致顺反异构特性,可调控聚合物的自组装行为而受到广泛关注。采用不同结构且广泛商业化的偶氮苯基小分子(偶氮苯(AZO)、对羟基偶氮苯(AZO-OH)、对氨基偶氮苯(AZO-NH2)、二甲基黄[AZO-N(CH_(3))_(2)])作为光分子开关,控制聚N-异丙基丙烯酰胺(PNIPAm)在1-乙基-3-甲基咪唑双(三氟甲基磺酰基)亚胺([C2mim][NTf_(2)])离子液体中的自组装行为,探讨不同偶氮苯基末端基元对于PNIPAm自组装相行为的影响。结果表明,偶氮苯基小分子均能有效调控PNIPAm在[C2mim][NTf_(2)]离子液体中的相变响应行为,但不同的末端基元对于PNIPAm的相变温度及相变区间影响甚微。结合原位变温红外谱图分析可知,紫外光照强化了PNIPAm与离子液体之间的相互作用,从而抑制了PNIPAm侧链间的相互聚集,这将促进紫外光照条件下“溶剂化”效应的发生,可获得更低的相变温度。 展开更多
关键词 偶氮苯 n-异丙基丙烯酰胺 离子液体 自组装 分子开关 相变 响应行为
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智能窗口用热响应聚(N-异丙基丙烯酰胺)水凝胶的研究进展
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作者 陈冠桦 程欣瑶 +3 位作者 翟迅 段文皓 王润东 于环洋 《化工技术与开发》 CAS 2024年第4期46-49,共4页
本文综述了智能窗口用热响应聚(N-异丙基丙烯酰胺)水凝胶的热响应机理,介绍了该水凝胶材料的制备方法及相关的性能,阐述了影响PTC效应的主要因素及提高其稳定性的方法,展望了智能窗口用热响应聚(N-异丙基丙烯酰胺)水凝胶未来的研究方向... 本文综述了智能窗口用热响应聚(N-异丙基丙烯酰胺)水凝胶的热响应机理,介绍了该水凝胶材料的制备方法及相关的性能,阐述了影响PTC效应的主要因素及提高其稳定性的方法,展望了智能窗口用热响应聚(N-异丙基丙烯酰胺)水凝胶未来的研究方向和发展前景。 展开更多
关键词 n-异丙基丙烯酰胺 水凝胶 智能窗口
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基于n型柔性半导体的有机晶体管及其电子-离子双响应特性
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作者 蒋浩 钟岳桁 +1 位作者 王刚 王宏志 《东华大学学报(自然科学版)》 CAS 北大核心 2024年第1期39-44,共6页
为了研究n型有机混合离子电子导体电子-离子双响应特性及分子量对载流子迁移率的影响,采用具有平面刚性的梯形分子链结构的高分子量聚苯并二咪唑苯并菲绕啉二酮制备高性能有机电化学晶体管,并对晶体管紫外可见吸收光谱和晶体管器件电气... 为了研究n型有机混合离子电子导体电子-离子双响应特性及分子量对载流子迁移率的影响,采用具有平面刚性的梯形分子链结构的高分子量聚苯并二咪唑苯并菲绕啉二酮制备高性能有机电化学晶体管,并对晶体管紫外可见吸收光谱和晶体管器件电气性能进行表征。结果表明,利用高分子量聚苯并二咪唑苯并菲绕啉二酮制备的n型有机电化学晶体管表现出极高的响应速度(0.034 s)、高载流子迁移率(4.72×10^(-3) cm^(2)/(V·s)),以及在水系电解液中优异的稳定性(稳定运行超过120次脉冲循环)。 展开更多
关键词 有机晶体管 n型柔性半导体 电子-离子双响应特性 聚苯并二咪唑苯并菲绕啉二酮 载流子迁移率
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聚N-异丙基丙烯酰胺/聚丙烯酸水凝胶的制备及性能研究
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作者 吴英 王书芳 +1 位作者 李雨露 戴杨雷 《山东化工》 CAS 2024年第1期38-41,共4页
当外界环境发生变化时,环境敏感型水凝胶的物理性质或化学性质会随之发生改变,大部分水凝胶对环境的响应比较单一。以丙烯酸(AA)和N-异丙基丙烯酰胺(NIPAm)为原料制备的聚N-异丙基丙烯酰胺/聚丙烯酸水凝胶既可以对温度变化也可以对pH值... 当外界环境发生变化时,环境敏感型水凝胶的物理性质或化学性质会随之发生改变,大部分水凝胶对环境的响应比较单一。以丙烯酸(AA)和N-异丙基丙烯酰胺(NIPAm)为原料制备的聚N-异丙基丙烯酰胺/聚丙烯酸水凝胶既可以对温度变化也可以对pH值变化做出响应。实验采用一锅法制备了聚N-异丙基丙烯酰胺/聚丙烯酸水凝胶,通过调节丙烯酸的中和度、丙烯酸(AA)和N-异丙基丙烯酰胺(NIPAm)两种单体的配比、交联剂N,N′-亚甲基双丙烯酰(BIS)和引发剂过硫酸钾(KPS)的用量,研究其对水凝胶的吸水性能、拉伸性能的影响,并考察了所制备的聚N-异丙基丙烯酰胺/聚丙烯酸水凝胶对温度及pH响应性能。实验结果表明:当丙烯酸的中和度为125%、n(NIPAm)∶n(AA)=0.3∶1、BIS的质量分数为0.5%、KPS的质量分数为1%时,制备的水凝胶溶胀率最大且有一定的弹性,室温下吸水率达179.73 g/g。该水凝胶在酸性缓冲溶液(pH值=3)中收缩,当缓冲溶液的pH值大于3,水凝胶发生溶胀,具有灵敏可逆的pH响应性能,同时该水凝胶兼具热缩温敏性能。 展开更多
关键词 聚丙烯酸 n-异丙基丙烯酰胺 水凝胶 PH值
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含PNIPAM嵌段有机纳米管的合成及其对MB与ARS的吸附与释放性能探究
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作者 王卓玉 施卜银 《宁夏工程技术》 CAS 2024年第2期124-131,共8页
为了高效吸附染料废水中的染料分子,制备了一种具有温度可控性的新型吸附材料。首先,采用可控自由基聚合和开环聚合将聚N-异丙基丙烯酰胺(PNIPAM)引入多孔有机纳米管中,制备了具有核壳结构的多组分聚合物分子刷;其次,利用分子刷嵌段聚... 为了高效吸附染料废水中的染料分子,制备了一种具有温度可控性的新型吸附材料。首先,采用可控自由基聚合和开环聚合将聚N-异丙基丙烯酰胺(PNIPAM)引入多孔有机纳米管中,制备了具有核壳结构的多组分聚合物分子刷;其次,利用分子刷嵌段聚合物的傅克烷基化超交联过程生成了具有微孔、中孔和大孔结构的PNIPAM修饰的多级孔有机纳米管网络(MONNs)聚合物;最后,探究了MONNs对染料分子亚甲基蓝(MB)、茜素红S(ARS)的吸附与释放性能。结果表明,该方法制备的MONNs材料对染料分子具有良好的吸附效果。 展开更多
关键词 n-异丙基丙烯酰胺 多级孔有机纳米管网络 吸附与释放性能 染料废水处理
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利用NVP组分调控亲水增强型温敏性PNIPAAm共聚物
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作者 范晓光 雷景胜 +3 位作者 顾诗雅 冷旭 刘畅 杨磊 《材料导报》 CSCD 北大核心 2023年第15期230-236,共7页
聚N-异丙基丙烯酰胺(PNIPAAm)是目前在生物医药领域研究和应用最为广泛的一种温敏性聚合物。但PNIPAAm均聚物的温敏性能相对单一,且由其构建的终产物难以在较宽温度范围内通过改变温度发生整体体积或表面润湿性能转变,因此限制了其应用... 聚N-异丙基丙烯酰胺(PNIPAAm)是目前在生物医药领域研究和应用最为广泛的一种温敏性聚合物。但PNIPAAm均聚物的温敏性能相对单一,且由其构建的终产物难以在较宽温度范围内通过改变温度发生整体体积或表面润湿性能转变,因此限制了其应用范围。为了扩展PNIPAAm的应用领域,设计可以调控特别是提升PNIPAAm基材最低临界溶液温度(LCST)的温敏性聚合物十分必要。鉴于此,本研究将亲水性N-乙烯基吡咯烷酮(NVP)引入温敏性聚合物分子骨架,同时利用共聚物的反应基团将P(NIPAAm-co-NVP)共聚物聚合接枝于铂片表面从而形成共聚物膜。衰减全反射-傅里叶变换红外光谱(ATR-FTIR)、核磁共振氢谱(1H-NMR)和凝胶渗透色谱(GPC)的鉴定结果表明各单体间的共聚反应均按预定方案进行,且可显著提升NVP在聚合过程的参与率;动态光散射(DLS)和静态接触角数据、扫描电子显微镜(SEM)图像均证明可以利用NVP组分提升P(NIPAAm-co-NVP)共聚物的LCST,从而获得亲水增强型的温敏性共聚物膜,该膜可用于药物控制释放和非侵害性细胞收获等。 展开更多
关键词 n-异丙基丙烯酰胺(PnIPAAm) n-乙烯基吡咯烷酮(nVP) 最低临界溶液温度(LCST) 自由基聚合法 亲水性
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磷酸掺杂磺化聚(亚芳基醚)-聚(N-乙烯基咪唑)膜电化学性能研究
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作者 史晋宜 魏庆玲 《化工生产与技术》 CAS 2023年第4期11-14,I0003,共5页
使用磺化聚芳基醚(SDF-F)作为酸性聚合物、聚(N-乙烯基咪唑)(PVIm)作为碱性聚合物,合成了用于高温工作的磷酸掺杂磺化聚(亚芳基醚)-聚(N-乙烯基咪唑)(SDF-F/PVIm)质子交换膜,进行了热损失、电导率、阻抗光谱和单电池性能测试。结果表明,... 使用磺化聚芳基醚(SDF-F)作为酸性聚合物、聚(N-乙烯基咪唑)(PVIm)作为碱性聚合物,合成了用于高温工作的磷酸掺杂磺化聚(亚芳基醚)-聚(N-乙烯基咪唑)(SDF-F/PVIm)质子交换膜,进行了热损失、电导率、阻抗光谱和单电池性能测试。结果表明,SDF-F/PVIm膜热稳定性良好。在无水条件下,交联膜在150~200℃具有很高的质子电导率,且电导率随着温度的升高而增加。在不同的温度下单电池的性能表现优异,在190℃时,可以获得528 mW/cm2最大功率密度,且无需外部加湿。合成的SDF-F/PVIm有望成为高温PEMFCs的新型聚合物电解质。 展开更多
关键词 磺化聚(亚芳基醚)-聚(n-乙烯基咪唑)质子交换膜 磷酸掺杂 电化学 性能
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Synthesis of Poly (3-acetylpyrrolyl methine) with Azobenzene Side Groups and Study on Its Third-order Nonlinear Optical Property 被引量:4
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作者 Zhigang ZHANG Hongcai WU +1 位作者 Lingjie MENG Wenhui YI 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2005年第5期715-718,共4页
A novel soluble π-conjugated polymer, poly [(3-acetylpyrrole-2, 5-diyl) p-(N, N-dimethylamino) azobenzylidene] (PAPDMAABE), was synthesized by condensation of 3-acetylpyrrole with 4-aldehyde-4'-dimethylaminoaz... A novel soluble π-conjugated polymer, poly [(3-acetylpyrrole-2, 5-diyl) p-(N, N-dimethylamino) azobenzylidene] (PAPDMAABE), was synthesized by condensation of 3-acetylpyrrole with 4-aldehyde-4'-dimethylaminoazobenzene (ADMAA). The chemical structure of PAPDMAABE was characterized by Fourier transform infrared spectroscopy (FTIR), ^1H-NMR, and UV-Vis-NIR spectra. Transmission electron microscope (TEM) analysis for PAPDMAABE indicates that part of PAPDMAABE is in crystal state, due to the short-range order of the polymer. Thermogravimetric analysis (TGA) curve shows that the polymer has good thermal stability and its decomposition temperature is 248℃. The optical band gap of PAPDMAABE obtained from the optical absorption spectrum is about 1.73 eV. The resonant third-order nonlinear optical property of PAPDMAABE at 532 nm was studied using degenerate four-wave mixing (DFWM) technique. The resonant third-order nonlinear optical susceptibility of the polymer is about 7.48×10^-8 esu. 展开更多
关键词 poly [(3-acetylpyrrole-2 5-diyl) p-(n n-dimethylamino) azobenzylidene] Small optical band gap Degenerate four-wave mixing Third-order nonlinear property
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Conformational Transition of Poly (Acrylic Acid) Detected by Microcantilever Sensing 被引量:6
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作者 李凯 刘红 +2 位作者 张青川 薛长国 伍小平 《Chinese Physics Letters》 SCIE CAS CSCD 2007年第6期1502-1504,共3页
Poly (acrylic acid) (PAA) chains are grafted on one side of a microcantilever by the self-assembled method and the deflections of the microcantilever are detected as a function of medium pH from 3 to 11. It is fou... Poly (acrylic acid) (PAA) chains are grafted on one side of a microcantilever by the self-assembled method and the deflections of the microcantilever are detected as a function of medium pH from 3 to 11. It is found that when the pH varies, the microcantilever deflects because of the changing surface stress. By analysing the electrostatic repulsive effect, the surface stress change is related to the conformation transition of PAA from a collapse state to a swelling state. This method offers the interaction information among the polymer chains during the conformational transition and affords an alternative way to study conformational change of polymers. 展开更多
关键词 poly(n-ISOPROPYLACRYLAMIDE) BRUSHES PH
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基于温敏性N,N-二甲基丙烯酰胺/N-异丙基丙烯酰胺无规共聚物的毛细管无胶电泳筛分介质 被引量:1
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作者 江凤浩 洪瀚 +1 位作者 姜伯玮 苏朝晖 《应用化学》 CAS CSCD 北大核心 2023年第9期1312-1321,共10页
本文合成了N,N-二甲基丙烯酰胺/N-异丙基丙烯酰胺无规共聚物(P(DMA-co-NIPAM))和聚N,N-二甲基丙烯酰胺(PDMA),并将二者共混制备毛细管无胶电泳筛分介质,旨在降低筛分介质粘度的同时增强其对DNA的分离性能。核磁共振氢谱(1H NMR)和傅里... 本文合成了N,N-二甲基丙烯酰胺/N-异丙基丙烯酰胺无规共聚物(P(DMA-co-NIPAM))和聚N,N-二甲基丙烯酰胺(PDMA),并将二者共混制备毛细管无胶电泳筛分介质,旨在降低筛分介质粘度的同时增强其对DNA的分离性能。核磁共振氢谱(1H NMR)和傅里叶变换红外光谱(FT-IR)证明了2种聚合物的成功合成。表征了P(DMA-co-NIPAM)/PDMA共混物溶液的流体力学直径(Dh)、低剪切粘度和吸光度,结果表明,P(DMAco-NIPAM)聚合物具有温敏性,低临界溶解温度(LCST)为60~80℃。DNA筛分结果显示,PDMA中添加了10%P(DMA-co-NIPAM)的复合筛分介质性能最好,相比PDMA粘度降低19%以上,对大DNA片段的分辨率和理论塔板数均明显提高,分离时间缩短4%,显示了优良的分离性能。 展开更多
关键词 毛细管电泳 毛细管无胶电泳筛分介质 DnA分离 温敏性聚合物 n n-二甲基丙烯酰胺
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Synthesis of Poly[(3-octanoylpyrrole-2,5-diyl)-p-(N,N-dimethylamino)benzylidene] and Its Properties by Nitrogen Ion Implantation 被引量:1
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作者 ZHANGZhi-gang WUHong-cai +1 位作者 LIUXiao-zeng YIWen-hui 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2005年第2期166-168,共3页
A novel soluble π-conjugated polymer, poly[(3-octanoylpyrrole-2,5-diyl)-p-(N,N-dimethylamino)benzylidene](POPDMABE), was synthesized firstly by the condensation of 3-octanoylpyrrole with para-dimethylaminobenzaldehyd... A novel soluble π-conjugated polymer, poly[(3-octanoylpyrrole-2,5-diyl)-p-(N,N-dimethylamino)benzylidene](POPDMABE), was synthesized firstly by the condensation of 3-octanoylpyrrole with para-dimethylaminobenzaldehyde. The chemical structure of the polymer was characterized by FTIR and 1H NMR spectrometries. The polymer is a potential nonlinear optical(NLO) material. According to the function of optical forbidden band gap(E_g) and photon energy(hν), the optical forbidden band gaps of the polymer before and after ion implantation were calculated. The resonant third-order nonlinear optical properties of POPDMABE before and after ion implantation were also studied by using the degenerate four-wave mixing(DFWM) technique at 532 nm. When the energy is 25 keV and the dose is 2.2×10 17 ions/cm 2, the {polymer′s} optical forbidden band gap is about 1.63 eV which is smaller than that of the non-implanted sample(1.98 eV) and the resonant third-order NLO susceptibility of POPDMABE is about 4.3×10 -7 esu, 1 order of magnitude higher than that of the non-implanted sample(4.1×10 -8 esu). The results show that nitrogen ion implantation is an effective method to improve the resonant third-order NLO property of the polymer. 展开更多
关键词 poly[(3-octanoylpyrrole-2 5-diyl)-p-(n n-dimethylamino)benzylidene] Ion implantation Optical forbidden band gap Resonant third-order nonlinear optical property Degenerate four-wave mixing technique
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A Temperature-sensitive Hydrogel Refolding System: Preparation of Poly(N-isopropyl acrylamide) and Its Application in Lysozyme Refolding 被引量:6
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作者 崔志芳 关怡新 姚善泾 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2004年第4期556-560,共5页
Temperature-sensitive hydrogel—poly(N-isopropyl acrylamide) (PNIPA) was prepared and applied to protein refolding. PNIPA gel disks and gel particles were synthesized by the solution polymerization and inverse suspens... Temperature-sensitive hydrogel—poly(N-isopropyl acrylamide) (PNIPA) was prepared and applied to protein refolding. PNIPA gel disks and gel particles were synthesized by the solution polymerization and inverse suspension polymerization respectively. The swelling kinetics of the gels was also studied. With these prepared PNIPA gels, the model protein lysozyme was renatured. Within 24h, PNIPA gel disks improved the yield of lysozyme activity by 49.3% from 3375.2U·mg^-1 to 5038.8U·mg^-1. With the addition of faster response PNIPA gel beads, the total lysozyme activity recovery was about 68.98% in 3h, as compared with 42.03% by simple batch dilution. The novel refolding system with PNIPA enables efficient refolding especially at high protein concentrations. Discussion about the mechanism revealed that when PNIPA gels were added into the refolding buffer, the hydrophobic interactions between denatured proteins and polymer gels could prevent the aggregation of refolding intermediates, thus enhanced the protein renaturation. 展开更多
关键词 温度 敏感性 水凝胶 聚乙烯 DnA 蛋白质 异丙基丙烯酰胺
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Synthesis and Characteristic of Poly(N-vinylacetamide) Containing Terbium Ion 被引量:3
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作者 蔡彦 陈明清 黄晓华 《Journal of Rare Earths》 SCIE EI CAS CSCD 2005年第2期230-234,共5页
Poly (N-vinylacetatnide) ( PNVA) was synthesized by free radical polymerization in ethanol solution, in which alpha, alpha'-azobisisobutyronitrile was used as an initiator. Tb(III)-PNVA polymer was prepared and ch... Poly (N-vinylacetatnide) ( PNVA) was synthesized by free radical polymerization in ethanol solution, in which alpha, alpha'-azobisisobutyronitrile was used as an initiator. Tb(III)-PNVA polymer was prepared and characterized by ultraviolet-visual (UV), fourier transform infrared (FIF-IR), X-ray photoelectron spectroscopy (XPS) and fluorescence spectroscopy. The experimental results of UV, FT-IR and XPS show that the Tb (III)-PNVA electrovalent complex is formed by electrostatic interaction between terbium (III) cation and complexible atoms of acylamino group in the pendant chain of the polymer. The fluorescence spectrum of the complex exhibits intensive characteristic emission of terbium at 490, 545 and 584 run, which are assigned to D-5(4)->F-7(6), D-5(6)->F-5(6) and D-5(4)->F-7(3) transition, indicating that there exists an efficient intermolecular energy transfer from the polymer ligand to the central rare earth ion. The emission intensity of the complex is increased with the increasing concentration of Tb (III) ion until the weight ratio of Tb (III) on to PNVA is 1.5% (mass fraction), and decreased with the further increasing concentration of Tb (III) ion, which is a typical concentration quenching behavior. 展开更多
关键词 TERBIUM poly ( n-vinylacetamide) energy transfer rare earths
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NOVEL AMPHIPHILIC FLUORESCENT GRAFT COPOLYMER: SYNTHESIS, CHARACTERIZATION AND ENCAPSULATION OF A HYDROPHOBIC AGENT 被引量:2
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作者 Zhao-qiang Wu Shu Yang Wen-yan Liao 孟令芝 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2006年第3期315-321,共7页
Novel amphiphilic fluorescent graft copolymer (PVP-PyAHy) was successfully synthesized by the free radical copolymerization of hydrophobic monomer N-(1-pyrenebutyryl)-N'-acryloyl hydrazide (PyAHy) with hydrophi... Novel amphiphilic fluorescent graft copolymer (PVP-PyAHy) was successfully synthesized by the free radical copolymerization of hydrophobic monomer N-(1-pyrenebutyryl)-N'-acryloyl hydrazide (PyAHy) with hydrophilic precursor polymers of vinyl-functionalized poly(N-vinylpyrrolidone) (PVP) in DMF. The copolymer is amphiphilic and has intrinsic fluorescence. FT-IR, ^1H-NMR, TEM, gel permeation chromatography-multi-angle laser light scattering, UV-Vis spectroscopy and fluorescence spectroscopy were used to characterize this copolymer. The TEM observation shows that the copolymer PVP-PyAHy forms micelles in aqueous solution. Results of fluorometric measurements illustrate that the critical micelle concentration (CMC) value of PVP-PyAHy in aqueous solution is about 0.90 mg/mL. To examine the encapsulation ability of the copolymer in aqueous media, methyl yellow was employed as a model hydrophobic agent. The loading level of the polymer to methyl yellow is 8.8 mg/g. The cytotoxicity assays for Madin Darby Canine Kidney (MDCK) cells shows good biocompatibility of PVP-PyAHy in vitro. These results suggest the potential of this copolymer PVP-PyAHy as drugs delivery carrier and fluorescent tracer. 展开更多
关键词 Amphiphilic copolymer FLUORESCEnCE polyn-vinylpyrrolidone).
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Y-shaped block copolymers of poly(ethylene glycol) and poly(N-isopropylacrylamide) synthesized by ATRP 被引量:2
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作者 Xin De Tang Xiao Chao Liang Nian Feng Han 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第11期1353-1356,共4页
Novel Y-shaped block copolymers of poly(ethylene glycol) and poly(N-isopropylacrylamide), PEG-b-(PNIPAM)2, were successfully synthesized through atom transfer radical polymerization (ATRP). A difunctional macr... Novel Y-shaped block copolymers of poly(ethylene glycol) and poly(N-isopropylacrylamide), PEG-b-(PNIPAM)2, were successfully synthesized through atom transfer radical polymerization (ATRP). A difunctional macroinitiator was prepared by esterification of 2,2-dichloroacetyl chloride with poly(ethylene glycol) monomethyl ether (PEG). The copolymers were obtained via the ATRP ofN-isopropylacrylamide (NIPAM) at 30℃ with CuCl/Me6TREN as a catalyst system and DMF/H2O (v/v = 3:1) mixture as solvent. The resulting copolymers were characterized by gel permeation chromatography (GPC) and ^1H NMR. These block copolymers show controllable molecular weights and narrow molecular weight distributions (PDI 〈 1.15). Their phase transition temperatures and the corresponding enthalpy changes in aqueous solution were measured by differential scanning calorimetry (DSC). As a result, the phase transition temperature of PEG45-b-(PNIPAM55)2 is higher than that of PNIPAM, however, the corresponding enthalpy change is much lower, indicating the significant influence of the macromolecular composition and architecture on the phase transition. 展开更多
关键词 Y-shaped Block copolymer poly(ethylene glycol) polyn-isopropylacrylamide) Atom transfer radical polymerization (ATRP)
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An easily recoverable thermo-sensitive polyelectrolyte as draw agent for forward osmosis process 被引量:4
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作者 Yanni Wang Hairong Yu +5 位作者 Rui Xie Kuangmin Zhao Xiaojie Ju Wei Wang Zhuang Liu Liangyin Chu 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2016年第1期86-93,共8页
As a potential solution to the crises of energy and resources, forward osmosis(FO) has been limited by the development of draw agents. An ideal draw agent should be able to generate high osmotic pressure and can be ea... As a potential solution to the crises of energy and resources, forward osmosis(FO) has been limited by the development of draw agents. An ideal draw agent should be able to generate high osmotic pressure and can be easily recovered. In this study, a thermo-sensitive polyelectrolyte of poly(N-isopropylacrylamide-co-acrylic acid)(PNA)is developed as an efficient draw agent, and two easy and simple methods are proposed to effectively recover the polyelectrolytes. After adjusting the pH value of polyelectrolyte solutions to around 6.0, the polyelectrolyte can generate relatively high osmotic pressure, and induce average water fluxes of 2.09 and 2.95 L·m^(-2)·h^(-1) during12 h FO processes when the polyelectrolyte concentrations are 0.20 and 0.38 g·ml^(-1) respectively. After acidifying and heating to 70 °C, the PNA-10 polyelectrolyte can aggregate together because of hydrophobic association and separate from water, so it can be easily recovered by either simple centrifugation or gravitational sedimentation. The recovery ratios of PNA-10 polyelectrolyte in both methods are as high as 89%, and the recovered polyelectrolytes can be reused with almost the same FO performance as fresh ones. The results in this study provide valuable guidance for designing efficient and easily recoverable draw agents for FO processes. 展开更多
关键词 聚电解质溶液 渗透过程 可回收 热敏感 n-异丙基丙烯酰胺 种用 高渗透压 电解质浓度
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Effect of Graft Yield on the Thermo-Responsive Permeability Through Porous Membranes with Plasma-Grafted Poly(N-isopropylacrylamide)Gates 被引量:6
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作者 褚良银 朱家骅 +3 位作者 陈文梅 NIITSUMA Takuya YAMAGUCHI Takeo NAKAO Shin-ichi 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2003年第3期269-275,共7页
The effect of graft yield on both the thermo-responsive hydraulic permeability and the thermo-respousive diffusional permeability through porous membranes with plasma-grafted poly(N-isopropylacrylamide) (PNIPAM)gates ... The effect of graft yield on both the thermo-responsive hydraulic permeability and the thermo-respousive diffusional permeability through porous membranes with plasma-grafted poly(N-isopropylacrylamide) (PNIPAM)gates was investigated. Both thermo-respousive flat membranes and core-shell microcapsule membranes with a wide range of graft yield of PNIPAM were prepared using a plasma-graft pore-filling polymerization method. The grafted PNIPAM was formed homogeneously throughout the entire thickness of both the fiat polyethylene membranes andthe microcapsule polyamide membranes. Both the hydraulic permeability and the diffusional permeability were heavily dependent on the PNIPAM graft yield. With increasing the graft yield, the hydraulic permeability (water flux) decreases rapidly at 25℃ because of the decrease of the pore size; however, the water flux at 40℃ increases firstly to a peak because of the increase of hydrophobicity of the pore surface, and then decreases and finally tends to zero because of the pore size becoming smaller and smaller. For the diffusional permeability, the temperature shows different effects on the diffusional permeability coefficients of solutes across the membranes. When the graft yield was low, the diffusional coefficient of solute across the membrane was higher at temperature above the lower critical solution temperature (LCST) than that below the LCST; however, when the graft yield was high, the diffusional coefficient was lower at temperature above the LCST than that below the LCST. It is very important to choose or design a proper graft yield of PNIPAM for obtaining a desired thermo-respousive 'on/off' hydraulic or ditfusional permeability. 展开更多
关键词 接枝量 温度效应 等离子体接枝 渗透性 多孔膜 聚(n-异丙基丙烯酰胺)
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SYNTHESIS OF POLYMER-STABILIZED RUTHENIUM COLLOIDS BY LOW BOILING POINT ALCOHOL REDUCTION 被引量:2
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作者 刘汉范 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2003年第1期1-4,共4页
Stable and well-dispersed poly(N-vinyl-2-pyrrolidone) (PVP)-stabilized ruthenium colloidal clusters wereprepaxed via the reduction of ruthenium(III) chloride by refluxing with low boiling point alcohols. Investigation... Stable and well-dispersed poly(N-vinyl-2-pyrrolidone) (PVP)-stabilized ruthenium colloidal clusters wereprepaxed via the reduction of ruthenium(III) chloride by refluxing with low boiling point alcohols. Investigation of the size ofRu colloids by transmission electron microscopy (TEM) indicated that the average diametes could be controlled in the rangeof 1.2-1.6 nm with relative standard deviations of less than 0.33 by changing the molar ratio of PVP to Ru. The X-rayphotoelectron spectroscopy (XPS) characterization verified the formation of elemental ruthenium colloids. 展开更多
关键词 polymer-stabilized colloid poly(n-vinyl-2-pyrrolidone) RUTHEnIUM Alcohol reduction
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