化学反应工程与工艺
化學反應工程與工藝
화학반응공정여공예
CHEMICAL REACTION ENGINEERING AND TECHNOLOGY
2015年
3期
271-276
,共6页
马彦洁%王平%杜淼%郑强
馬彥潔%王平%杜淼%鄭彊
마언길%왕평%두묘%정강
自由基胶束共聚%疏水改性聚两性电解质%聚磺酸甜菜碱
自由基膠束共聚%疏水改性聚兩性電解質%聚磺痠甜菜堿
자유기효속공취%소수개성취량성전해질%취광산첨채감
free radical micellar copolymerization%hydrophobically modified polyampholyte%copolymerization conditions
疏水改性聚磺酸甜菜碱具有超亲水、抗蛋白吸附、环境友好等性能,在药物缓释、化妆品、器官移植、食品包装等领域潜在应用价值巨大。采用自由基胶束共聚法合成了具有疏水嵌段的聚磺酸甜菜碱共聚物,亲水单体为[2-(甲基丙烯酰基氧基)乙基]二甲基-(3-磺酸丙基)氢氧化铵(SBMA),疏水单体为甲基丙烯酸缩水甘油酯(GMA),探究了聚合条件对共聚物结构及性质的影响。研究发现,引发剂用量较高时,SBMA的含量相对较高。当GMA用量较少时,SBMA含量随乳化剂用量的增加而下降;当GMA用量较大时,乳化剂用量对共聚物中 SBMA 含量影响不显著。搅拌速率增加后,共聚物水溶液的表观粘度(ηa)和 SBMA 含量均逐渐下降。GMA 用量增大后,疏水嵌段长度及数量均增大。相同单体投料比下,乳化剂用量越大,形成的GMA胶束数量越多,共聚后形成的疏水嵌段长度越短,数量越多。P(SBMA-GMA)大分子在水中以胶束形式存在。自由基胶束聚合得到的P(SBMA-GMA)共聚物的分子量高于SBMA均聚物。以上研究结果可为疏水改性聚两性电解质的制备工艺优化提供参考。
疏水改性聚磺痠甜菜堿具有超親水、抗蛋白吸附、環境友好等性能,在藥物緩釋、化妝品、器官移植、食品包裝等領域潛在應用價值巨大。採用自由基膠束共聚法閤成瞭具有疏水嵌段的聚磺痠甜菜堿共聚物,親水單體為[2-(甲基丙烯酰基氧基)乙基]二甲基-(3-磺痠丙基)氫氧化銨(SBMA),疏水單體為甲基丙烯痠縮水甘油酯(GMA),探究瞭聚閤條件對共聚物結構及性質的影響。研究髮現,引髮劑用量較高時,SBMA的含量相對較高。噹GMA用量較少時,SBMA含量隨乳化劑用量的增加而下降;噹GMA用量較大時,乳化劑用量對共聚物中 SBMA 含量影響不顯著。攪拌速率增加後,共聚物水溶液的錶觀粘度(ηa)和 SBMA 含量均逐漸下降。GMA 用量增大後,疏水嵌段長度及數量均增大。相同單體投料比下,乳化劑用量越大,形成的GMA膠束數量越多,共聚後形成的疏水嵌段長度越短,數量越多。P(SBMA-GMA)大分子在水中以膠束形式存在。自由基膠束聚閤得到的P(SBMA-GMA)共聚物的分子量高于SBMA均聚物。以上研究結果可為疏水改性聚兩性電解質的製備工藝優化提供參攷。
소수개성취광산첨채감구유초친수、항단백흡부、배경우호등성능,재약물완석、화장품、기관이식、식품포장등영역잠재응용개치거대。채용자유기효속공취법합성료구유소수감단적취광산첨채감공취물,친수단체위[2-(갑기병희선기양기)을기]이갑기-(3-광산병기)경양화안(SBMA),소수단체위갑기병희산축수감유지(GMA),탐구료취합조건대공취물결구급성질적영향。연구발현,인발제용량교고시,SBMA적함량상대교고。당GMA용량교소시,SBMA함량수유화제용량적증가이하강;당GMA용량교대시,유화제용량대공취물중 SBMA 함량영향불현저。교반속솔증가후,공취물수용액적표관점도(ηa)화 SBMA 함량균축점하강。GMA 용량증대후,소수감단장도급수량균증대。상동단체투료비하,유화제용량월대,형성적GMA효속수량월다,공취후형성적소수감단장도월단,수량월다。P(SBMA-GMA)대분자재수중이효속형식존재。자유기효속취합득도적P(SBMA-GMA)공취물적분자량고우SBMA균취물。이상연구결과가위소수개성취량성전해질적제비공예우화제공삼고。
Hydrophobically modified polysulfobetaines exhibit superhydrophilicity, anti-protein adsorption and are environmentally friendly, which have potential applications in drug delivery, cosmetic, organ transplantation, food packaging and so on. In this work, polysulfobetaine methacrylate (PSBMA) hydrophobically modified with methacrylic acid 2,3-epoxypropyl ester (GMA) was synthesized via a free radical micellar copolymerization method. Effect of reaction condition upon the properties of the copolymer such as apparent viscosity of the copolymer aqueous solution and the yield were investigated. Experimental results showed that the content of SBMA was higher as the content of initiator was increased. When GMA content was low, the amount of SBMA decreased with increasing surfactant amount. However, the amount of SBMA was slightly influenced by the amount of surfactant in the case of high content GMA. Both the viscosity of the copolymer aqueous solution and the SBMA content decreased with the increase of stirring speed. The length and content of hydrophobic block segments were enlarged as GMA content was increased. Under the same ratio of SBMA/GMA monomers, increasing the amount of emulsifier increased the amount of GMA micelle and the content of hydrophobic block in copolymer. P(SBMA-GMA) copolymer chains were in the form of micelles in water, and the number molecular weight of P(SBMA-GMA) was higher than that of PSBMA.