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SYNTHESIS OF STYRENIC TONER PARTICLES BY SPG EMULSIFICATION TECHNIQUE 被引量:2
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作者 Suda Kiatkamjornwong Roongkan Nuisin +1 位作者 Guang-HuiMa Shinzo Omi 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2000年第4期309-322,共14页
This research studied the initiator efficiency for producing polymeric particles of poly(styrene-co-methyl methacrylate)copolymers by a Shirasu porous glass membrane(SPG)emulsification technique followed by suspension... This research studied the initiator efficiency for producing polymeric particles of poly(styrene-co-methyl methacrylate)copolymers by a Shirasu porous glass membrane(SPG)emulsification technique followed by suspension copolymerization.BPO,ADVN,and AIBN were used as initiators and we found that BPO is the most suitable initiator.Copolymers for various feed ratios of styrene/methyl methacrylate were thus synthesized by benzoyl peroxide,and their copolymer particle size,molecular weight distribution and pat-ride size distribution were characterized.Then n-BMA or 2-EHMA was added as the third monomer to decrease the terpolymer glass transition temperature.This article describes the preparation technique,recipes and polymerization conditions for producing both copolymer and terpolymer particles,particle size changes,the corresponding particle morphologies and glass transition temperatures. 展开更多
关键词 shirasu porous glass emulsification n-butyl methacrylate 2-ethylhexyl methacrylate toner binder
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CONTROL OF POLYMER PARTICLE SIZE USING POROUS GLASS MEMBRANE EMULSIFICATION A REVIEW 被引量:4
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作者 Guanghui Ma State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100080, P. R. China Tel: 0086-10-82627072, ghma@home.ipe.ac.cn 《China Particuology》 SCIE EI CAS CSCD 2003年第3期105-114,共10页
Much attention has in recent years been paid to fine applications of polymer particles, e.g., carrier for enzyme, separation media for protein, DNA and cell, and carrier for drug in Drug Delivery System (DDS). Control... Much attention has in recent years been paid to fine applications of polymer particles, e.g., carrier for enzyme, separation media for protein, DNA and cell, and carrier for drug in Drug Delivery System (DDS). Control of polymer particle size is especially important in such fine applications. For instance, when the particles are used as a carrier of anti-cancer agents, the locations of particles containing anti-cancer agents also depend on the size of the particles. In this paper, various techniques of controlling polymer particle size are described, with emphasis on Shirasu Porous Glass (SPG) membrane emulsification, as carried out in our research group. 展开更多
关键词 PARTICLES POLYMERIZATION emulsification shirasu porous glass membrane MICROCAPSULE
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W/O/W复乳溶剂蒸发法制备微胶囊的影响因素及研究新进展 被引量:9
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作者 曹梅 管萍 +1 位作者 胡小玲 陈晓佩 《化学与生物工程》 CAS 2009年第9期1-6,10,共7页
重点综述了W/O/W复乳溶剂蒸发法制备微胶囊的过程及影响因素,并结合SPG膜乳化法阐述了其最新研究进展。
关键词 W/O/W复乳液 复乳溶剂蒸发法 微胶囊 SPG膜乳化法
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STUDY ON PREPARATION OF UNIFORM POLYSTYRENE HOLLOW PARTICLES
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作者 Ma Guanghui and Omi Shinzo (Tokyo University of Agriculture and Technology, Nakamachi 2-24-16, Koganei, Tokyo 184-8588, Japan) 《化工学报》 EI CAS CSCD 北大核心 2000年第S1期35-38,共4页
Uniform polystyrene hollow particles were prepared successfully by employing SPG (Shirasu porous glass) emulsification technique. The oil phase composed of monomer [styrene (St) and N,N’-dimethylamino ethylmethacryla... Uniform polystyrene hollow particles were prepared successfully by employing SPG (Shirasu porous glass) emulsification technique. The oil phase composed of monomer [styrene (St) and N,N’-dimethylamino ethylmethacrylate (DMAEMA)], hexadecane (HD) and initiator was permeated through the uniform pores of SPG membrane into the aqueous phase (containing stabilizer, emulsifier and water-soluble inhibitor ) by a gas pressure to form uniform droplets. The droplets were then polymerized at 70℃. It was found that the hollow particles were obtained by adding a small amount of DMAEMA into the oil phase and by using NaNo2 as the water-soluble inhibitor, while only one-hole particles were obtained without adding DMAEMA, or when using diaminophenylene (DAP) or hydroquinone (HQ) as the inhibitor. The formation mechanism was discussed by the view of interfacial tensions between polymer and aqueous phase, HD and aqueous phase, and HD and polymer. Further more, it was found that hollow particles can be obtained even when DMAEMA content in the oil phase was very low, by increasing HD to high value. 展开更多
关键词 shirasu porous glass emulsification hollow particle POLYSTYRENE N N’-dimethylmino ethylmethacrylate
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膜乳化法制备单分散性载羟基喜树碱缓释微球
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作者 张其清 侯振清 +2 位作者 王衍戈 韩晶 林程宏 《国际生物医学工程杂志》 CAS 北大核心 2009年第1期1-4,共4页
目的 研究利用微孔膜乳化法制备载抗癌药10-羟基喜树碱(IqCPT)缓释微球的可行性。方法 以HCPT为模型药物,聚乳酸(PEA)为载体,以膜乳化法制备载药微球,并研究制剂的表面形态、载药率、包封率和缓释效果等性质。结果 膜乳化法制备... 目的 研究利用微孔膜乳化法制备载抗癌药10-羟基喜树碱(IqCPT)缓释微球的可行性。方法 以HCPT为模型药物,聚乳酸(PEA)为载体,以膜乳化法制备载药微球,并研究制剂的表面形态、载药率、包封率和缓释效果等性质。结果 膜乳化法制备的载HCPT聚乳酸微球,粒径可控制在1-10μm之间。表面圆整,稳定性、单分散性良好,载药率和包封率最高分别可达32.7%和81.7%,24h体外累积释放量为17.3%。结论 膜乳化法制备的载HCPT微球制剂均匀分散,具有明显缓释效果,是制备缓释微球制剂的较好方法。 展开更多
关键词 10-羟基喜树碱 膜乳化法 聚乳酸微球 载药系统
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