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复合 PNIPAM/二氧化硅微胶囊的内部微观结构和温敏性能研究。

Investigation of internal microstructure and thermo-responsive properties of composite PNIPAM/silica microcapsules.

机构信息

Chemical Robotics Laboratory, Department of Chemical Engineering, Institute of Chemical Technology Prague, Technická 3, 166 28 Prague 6, Czech Republic.

出版信息

J Colloid Interface Sci. 2010 Jun 15;346(2):352-60. doi: 10.1016/j.jcis.2010.02.060. Epub 2010 Mar 3.

Abstract

Composite microcapsules consisting of a thermo-responsive hydrogel poly-N-isopropylacrylamide (PNIPAM) and coated by silica (SiO(2)) nanoparticles have been synthesized by the inverse Pickering emulsion polymerization method. The composite capsules, whose mean diameter is in the 25-86 microm range in the expanded state, were characterized by static light scattering, atomic force microscopy (AFM), scanning electron microscopy (SEM), and laser scanning confocal microscopy (LSCM). It is reported that the hydrogel surface is uniformly covered by a monolayer of silica nanoparticles and that depending on the capsule size and degree of polymer cross-linking, either hollow-core or partially-filled hydrogel-core microcapsules can be created. Equilibrium thermo-responsive behavior of the composite microcapsules is investigated and it is found that after heating the particles above the lower critical solution temperature (LCST) of PNIPAM, the shrinkage ratio V/V(max) varies from 0.8 to 0.4 for a cross-linking ratio from 0.6% to 9% on a mass basis. Dynamic temperature cycling studies reveal no hysteresis in the shrinking and recovery phases, but a small measurable dependence of the asymptotic shrinkage ratio V/V(max) on the rate of temperature change exists. The composite capsules are stable under long-term storage in both dried and hydrated states and easily re-dispersible in water.

摘要

由温敏水凝胶聚 N-异丙基丙烯酰胺(PNIPAM)和二氧化硅(SiO(2))纳米粒子组成的复合微胶囊通过反相 Pickering 乳液聚合方法合成。复合胶囊在膨胀状态下的平均直径在 25-86 微米范围内,通过静态光散射、原子力显微镜(AFM)、扫描电子显微镜(SEM)和激光扫描共聚焦显微镜(LSCM)进行了表征。据报道,水凝胶表面均匀地覆盖着一层二氧化硅纳米粒子,并且根据胶囊的大小和聚合物交联度的不同,可以形成空心核或部分填充的水凝胶核微胶囊。研究了复合微胶囊的平衡热响应行为,发现将粒子加热到 PNIPAM 的下临界溶液温度(LCST)以上后,交联比为 0.6%至 9%(按质量计)时,收缩率 V/V(max)从 0.8 变化到 0.4。动态温度循环研究表明,在收缩和恢复阶段没有滞后,但存在渐近收缩率 V/V(max)对温度变化率的微小可测量依赖性。复合胶囊在干燥和水合状态下长期储存下稳定,并且在水中易于再分散。

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