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The Effect of Cyclodextrins in Polymer Particles Synthesis 被引量:2
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作者 JieHU BaiLingLIU 《Chinese Chemical Letters》 SCIE CAS CSCD 2004年第4期459-462,共4页
The free radical polymerization of styrene in water in the presence of β-cyclodextrin (β-CD) is described. It is found that β-CD could greatly accelerate the polymerization, enhance the final conversion of monomer.... The free radical polymerization of styrene in water in the presence of β-cyclodextrin (β-CD) is described. It is found that β-CD could greatly accelerate the polymerization, enhance the final conversion of monomer. The particle-size distribution of the final polymer is also improved than that without β-CD in the system. 展开更多
关键词 CYCLODEXTRIN polymerization conversion polymer particles.
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Synthesis of crystals and particles by crystallization and polymerization in droplet-based microfluidic devices 被引量:1
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作者 Jingtao WANG Jin ZHANG Junjie HAN 《Frontiers of Chemical Science and Engineering》 SCIE EI CSCD 2010年第1期26-36,共11页
The recent advances in crystallization and polymerization assisted by droplet-based microfluidics to synthesize micro-particles and micro-crystals are reviewed in this paper.Droplet-based microfluidic devices are powe... The recent advances in crystallization and polymerization assisted by droplet-based microfluidics to synthesize micro-particles and micro-crystals are reviewed in this paper.Droplet-based microfluidic devices are powerful tools to execute some precise controls and operations on the flow inside microchannels by adjusting fluid dynamics parameters to produce monodisperse emulsions or multiple-emulsions of various materials.Major features of this technique are producing particles of monodispersity to control the shape of particles in a new level,and to generate droplets of diverse materials including aqueous solutions,gels and polymers.Numerous microfluidic devices have been employed to generate monodisperse droplets of range from nm toμm,such as T junctions,flow-focusing devices and co-flow or cross-flow capillaries.These discrete,independently controllable droplets are ideal microreactors to be manipulated in the channels to synthesize the nanocrystals,protein crystals,polymer particles and microcapsules.The generated monodisperse particles or crystals are to meet different technical demands in many fields,such as crystal engineering,encapsulation and drug delivery systems.Microfluidic devices are promising tools in the synthesis of micron polymer particles that have diverse applications such as the photonic materials,ion-exchange and chromatography columns,and field-responsive rheological fluids.Processes assisted by microfluidic devices are able to produce the polymer particles(including Janus particles)with precise control over their sizes,size distribution,morphology and compositions.The technology of microfluidics has also been employed to generate core-shell microcapsules and solid microgels with precise controlled sizes and inner structures.The chosen“smart”materials are sensitive to an external stimulus such as the change of the pH,electric field and temperature.These complex particles are also able to be functionalized by encapsulating nanoparticles of special functions and by attaching some special groups like targeting ligands.The nucleation kinetics of some crystals like KNO_(3)was investigated in different microfluidic devices.Because of the elimination of the interactions among crystallites in bulk systems,using independent droplets may help to measure the nucleation rate more accurately.In structural biology,the droplets produced in microfluidic devices provide ideal platforms for protein crystallization on the nanoliter scale.Therefore,they become one of the promising tools to screen the optimal conditions of protein crystallization. 展开更多
关键词 MICROFLUIDICS emulsion polymerization polymer particle micro-capsule drug delivery emulsion crystallization nucleation kinetics protein crystallization
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Selective removal of phenol by spherical particles of α-,β- and γ-cyclodextrin polymers: kinetics and isothermal equilibrium 被引量:1
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作者 Qingchuan CHEN Yicun WEN Yu CANG Li LI Xuhong GUO Rui ZHANG 《Frontiers of Chemical Science and Engineering》 SCIE EI CAS CSCD 2013年第2期162-169,共8页
Spherical particles of α-,β- and γ-cyclodextrin (CD) polymers to efficiently remove phenol from waste water were prepared by reverse suspension polymerization with epichlorohydrin as crosslinker in liquid paraffi... Spherical particles of α-,β- and γ-cyclodextrin (CD) polymers to efficiently remove phenol from waste water were prepared by reverse suspension polymerization with epichlorohydrin as crosslinker in liquid paraffin. By controlling the amounts of crosslinker and water, well- defined spherical polymer particles with controllable size were obtained. Due to the selective inclusion associations between CD groups and phenol, these CD spherical polymer particles were demonstrated to be ideal candidates for removal of phenol. Among them β-CD polymer particles showed the best performance. The kinetics and isothermal equilibrium models were used to fit the experimental data of phenol removal from aqueous solution using these CD polymer particles. It was found that the kinetics followed the Ho and Mckay equation, suggesting that the adsorption process of phenol was controlled by diffusion and the host-guest interaction between CD and phenol. Equilibrium isothermal data can be well fitted by the Freundlich equation. The negative free energy change indicated the spontaneous nature of adsorption of phenol by α-,β- and γ-CD spherical polymer particles, while the lowest free energy for β-CD polymer reflected its best adsorption ability, compared to α- and γ- CD polymer particles. 展开更多
关键词 cyclodextrin polymer particles phenol kinetic models adsorption isotherm equilibrium models
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2023年我国丁二烯市场预测
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《合成橡胶工业》 CAS 北大核心 2023年第2期104-104,共1页
据合成橡胶工业协会网站3月28日报道,进入2023年,国内丁二烯行情大幅走高,市场价格环比增加22.71%,同比增幅达44.76%。2023年丁二烯市场偏紧格局将持续,行情值得期待,同时国内丁二烯市场整体运行区间或将略高于2022年,整体将高位运行。... 据合成橡胶工业协会网站3月28日报道,进入2023年,国内丁二烯行情大幅走高,市场价格环比增加22.71%,同比增幅达44.76%。2023年丁二烯市场偏紧格局将持续,行情值得期待,同时国内丁二烯市场整体运行区间或将略高于2022年,整体将高位运行。从2023年丁二烯产能释放情况来看,全年或有1 040 kt新产能释放,但不排除部分装置延后投产。同时,本应2022年年底投运的新装置多数延至今年上半年投产。2023年上半年受新产能集中释放影响,丁二烯供应趋紧的利好将逐步消散,市场或呈现高开低走态势。预计下半年丁二烯新装置投产数量有限。 展开更多
关键词 高开低走 利好 市场预测 环比增加 丁二烯 运行区间 偏紧格局 高位运行
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丁二烯-丙烯腈-丙烯酸丁酯三元共聚物的制备及性能
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作者 史工昌 钟启林 +2 位作者 王永峰 杨海龙 赵志超 《合成橡胶工业》 CAS 北大核心 2023年第2期100-104,共5页
采用乳液聚合法制备了丁二烯-丙烯腈-丙烯酸丁酯三元共聚物(BNBR),考察了引发剂、乳化剂及相对分子质量调节剂用量对乳液聚合反应速率的影响,并对BNBR的微观结构和动态力学性能进行了表征。结果表明,随着聚合温度的升高,BNBR的反应速率... 采用乳液聚合法制备了丁二烯-丙烯腈-丙烯酸丁酯三元共聚物(BNBR),考察了引发剂、乳化剂及相对分子质量调节剂用量对乳液聚合反应速率的影响,并对BNBR的微观结构和动态力学性能进行了表征。结果表明,随着聚合温度的升高,BNBR的反应速率明显加快,反应诱导期缩短。引发剂及乳化剂用量的增加均可提高反应速率,而相对分子质量调节剂用量的变化对反应速率影响不大。BNBR共聚体系的表观反应活化能为27.97 kJ/mol,BNBR胶乳粒径分布均匀。BNBR的玻璃化转变温度低于丁腈橡胶(NBR),二者相差约10℃,BNBR在低温下的动态力学性能优于NBR。 展开更多
关键词 丁二烯-丙烯腈-丙烯酸丁酯三元共聚物 乳液聚合 聚合反应动力学 微观结构 粒径分布 动态力学性能
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偶氮二异丁腈引发甲基丙烯酸甲酯微乳液聚合 被引量:10
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作者 徐相凌 葛学武 +3 位作者 张志成 张曼维 左榘 牛爱珍 《中国科学技术大学学报》 CAS CSCD 北大核心 2000年第1期62-68,共7页
以一种新的Y型乳化剂 1 2 丁酰氧基 9 十八烯酸 (BOA) ,制备了甲基丙烯酸甲酯 (MMA)含量高达 2 0 %的微乳液 ,并以油溶性引发剂偶氮二异丁腈 (AIBN)引发其聚合 .实验表明 ,与单体含量较低的微乳液聚合相比 ,MMA在其含量较高的微乳液... 以一种新的Y型乳化剂 1 2 丁酰氧基 9 十八烯酸 (BOA) ,制备了甲基丙烯酸甲酯 (MMA)含量高达 2 0 %的微乳液 ,并以油溶性引发剂偶氮二异丁腈 (AIBN)引发其聚合 .实验表明 ,与单体含量较低的微乳液聚合相比 ,MMA在其含量较高的微乳液中聚合时表现出一些明显不同的特征 ,如在聚合初期 ,聚合主要在大粒子内进行 .MMA的聚合与非极性单体的微乳液聚合相比也比较特殊 ,其聚合速度和聚合物分子量与引发剂浓度、单体浓度及乳化剂浓度的关系如下 :Rp ∝ [AIBN]0 .83 [MMA ]0 .49[BOA]-0 .98,Mn ∝ [AIBN]-0 .2 9[MMA]0 .61[BOA]-0 .2 2 . 展开更多
关键词 微乳液聚合 甲基丙烯酸甲酯 引发 偶氮二异丁腈
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β环糊精对苯乙烯无皂乳液聚合的影响 被引量:4
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作者 胡杰 李元杰 +1 位作者 吉海燕 陈正南 《高分子学报》 SCIE CAS CSCD 北大核心 2007年第3期246-249,共4页
以苯乙烯为单体,过硫酸钾为引发剂,研究了β环糊精对无皂乳液聚合反应的影响.结果表明,环糊精的引入可以大大加快反应速度,提高单体转化率,并且反应速度随环糊精加入量的增加而增大;同时,环糊精的引入能够减小制得的聚合物微球的粒度分... 以苯乙烯为单体,过硫酸钾为引发剂,研究了β环糊精对无皂乳液聚合反应的影响.结果表明,环糊精的引入可以大大加快反应速度,提高单体转化率,并且反应速度随环糊精加入量的增加而增大;同时,环糊精的引入能够减小制得的聚合物微球的粒度分布,使聚合物微球的粒径大小更加均匀,而对粒径的影响不是很大.动力学分析的结果表明,环糊精可以提高单体的反应活性.当环糊精/单体比例增大到0.2时,单体反应活性是空白体系的3.3倍. 展开更多
关键词 环糊精 聚合反应 聚合物微球 动力学
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苯乙烯-甲基丙烯酸甲酯悬浮-乳液耦合聚合动力学 被引量:1
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作者 张震乾 包永忠 +1 位作者 黄志明 翁志学 《化工学报》 EI CAS CSCD 北大核心 2005年第11期2207-2211,共5页
采用苯乙烯(St)悬浮聚合过程滴加甲基丙烯酸甲酯(MMA)乳液聚合组分,进行悬浮-乳液耦合聚合(SECP),制备大粒径聚苯乙烯-聚甲基丙烯酸甲酯(PS-PMMA)复合粒子.采用1H NMR分析方法,讨论了SECP动力学特征.St的SECP聚合速率和转化率与悬浮聚... 采用苯乙烯(St)悬浮聚合过程滴加甲基丙烯酸甲酯(MMA)乳液聚合组分,进行悬浮-乳液耦合聚合(SECP),制备大粒径聚苯乙烯-聚甲基丙烯酸甲酯(PS-PMMA)复合粒子.采用1H NMR分析方法,讨论了SECP动力学特征.St的SECP聚合速率和转化率与悬浮聚合一致;MMA聚合速率决定于乳胶粒子聚合速度和凝并在悬浮粒子表面的速度,聚合速率比常规乳液聚合速率低.由于凝并在悬浮粒子表面的PMMA乳胶粒子不再有乳液聚合特征,MMA在SECP中转化率低于同条件常规乳液聚合.分别得到乳化剂和引发剂浓度与SECP和普通乳液聚合恒速段聚合速率的关系. 展开更多
关键词 悬浮-乳液耦合聚合 聚苯乙烯 聚甲基丙烯酸甲酯 复合粒子 动力学
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无规甲基化β-环糊精对甲基丙烯酸甲酯无皂乳液聚合影响 被引量:2
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作者 杨学红 胡杰 +1 位作者 周志平 魏伟 《精细化工》 EI CAS CSCD 北大核心 2011年第2期111-115,共5页
采用溶液法制备了无规甲基化β-环糊精(RAMEB)/甲基丙烯酸甲酯(MMA)包合物,利用紫外-可见光谱、热重-差热分析等检测手段表明RAMEB与MMA可以形成摩尔比为1∶1的包合物,从而使MMA的热稳定性大大提高。通过RAMEB与MMA的包合作用研究了RAME... 采用溶液法制备了无规甲基化β-环糊精(RAMEB)/甲基丙烯酸甲酯(MMA)包合物,利用紫外-可见光谱、热重-差热分析等检测手段表明RAMEB与MMA可以形成摩尔比为1∶1的包合物,从而使MMA的热稳定性大大提高。通过RAMEB与MMA的包合作用研究了RAMEB对MMA无皂乳液聚合反应的影响。结果表明,当RAMEB的加入量为4.2×10-4mol时,体系在75℃反应30 min时,单体转化率达89.2%,比同一时间下没有加入RAMEB的空白样的单体转化率提高了30.6%。当RAMEB的加入量为8.4×10-4mol时,聚合反应速率比空白样低,单体的最终转化率与空白样差不多。同时,RAMEB的引入可以使PMMA微球粒径变大,随着RAMEB加入量的增加,聚合物微球的大小越来越均匀。 展开更多
关键词 甲基丙烯酸甲酯 无规甲基化β-环糊精 包合物 无皂乳液聚合 聚合物微球 功能材料
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