采用三相界面聚合法，对聚合单体进行筛选，对聚合条件进行优化。
The use of three-phase interfacial polymerization, polymerization of monomer on the screen to optimize the polymerization conditions.
以己二酰氯-三乙烯四胺为壁材，四氯乙烯为芯材，通过界面聚合法制备微胶囊。
Microcapsules were prepared by interfacial polymerization, with adipoyl chloride-triethylenetetramine as wall material, and tetrachloroethylene as core material.
方法：采用均匀设计方法设计实验，以界面聚合法制备出阿克拉霉素A聚乳酸毫微粒。
METHODS: An optimal design was selected to establish the optimal condition, and the interfacial polymerization method was used to prepare the nanoparticle system.
介绍了电泳显示微胶囊的构成及常用制备方法（原位聚合法、界面聚合法及复凝聚法）。
Composition and common preparation methods of microcapsules for electrophoretic display, such as in-situ polymerization, interface polymerization and recoagulation, were introduced.
采用三相界面聚合法能够制备出表面相对光滑的高脱盐、高水通量的新型复合型反渗透膜。
The use of three-phase interfacial polymerization can be prepared by a relatively smooth surface of high-desalination, high water flux of the new composite reverse osmosis membrane.
摘要研究了界面聚合法制备微胶囊阻燃剂时，分散剂用量、搅拌速度等因素对微胶囊粒径大小及分布的影响规律。
During making microcapsule by interfacial polymerization process the effects of the agitation speed dispersant dosage on the size and distribution of microcapsule particle diameter were investigated.
本论文采用界面聚合法制备聚脲微胶囊并将分散染料微胶囊用于热溶染色、转移印花、多色多点印花和双面印花等。
Disperse dye microcapsules were applied in thermosol dyeing, transfer printing, multi-color and multi-dot printing and double sided printings.
实验中采用界面聚合法制备聚酰胺多孔微囊，然后利用等离子体接枝填孔聚合法将PNIPAM接枝在微囊壁的膜孔中。
Interfacial polymerization was introduced to prepare polyamide porous microcapsules, and plasma-graft pore-filling polymerization was used to graft PNIPAM into the pore of the microcapsule membranes.
利用界面聚合法制备了亚微米级染料前体微胶囊和显色剂微胶囊，探讨了显影条件、囊壁材料用量与影像密度之间的关系。
The relationship between developing conditions and image density, as well as the weight of microcapsule wall material and image density were obtained.
概述了复合凝聚法、乳液聚合法、界面和原位聚合法、锐孔 凝固浴法等胶囊化的主要方法及其进展。
Methods and theories of the preparation of microcapsule were reviewed. Some approaches methods, such as heterocoagulation, emulsion polymerization etc.
概述了复合凝聚法、乳液聚合法、界面和原位聚合法、锐孔 凝固浴法等胶囊化的主要方法及其进展。
Methods and theories of the preparation of microcapsule were reviewed. Some approaches methods, such as heterocoagulation, emulsion polymerization etc.
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