检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:陈艳军[1] 张钰英[1,2] 王艺峰[1] 罗文[1]
机构地区:[1]武汉理工大学材料科学与工程学院高分子材料系,武汉430070 [2]河南省洛阳市嵩县何村乡政府,洛阳471400
出 处:《高分子学报》2010年第12期1437-1443,共7页Acta Polymerica Sinica
基 金:国家青年科学基金(基金号50803048);武汉市青年科技晨光计划(项目号200750731269)资助项目
摘 要:通过可逆加成-断链链转移(RAFT)溶液聚合,以三硫代碳酸酯为RAFT试剂,偶氮二异丁腈(AIBN)为引发剂,1,4-二氧六环为溶剂,制备甲基丙烯酸(2,2,2-三氟)乙酯(TFEMA)和苯乙烯(St)共聚物.详细研究了不同引发剂的用量、RAFT试剂与引发剂摩尔比以及聚合温度等实验条件对聚合反应过程的影响.通过GPC、FTIR测试共聚物的分子量、分子量分布和分子结构,并用静态接触角仪和AFM分别表征聚合物膜的接触角、表面能及膜的表面形貌.The copolymers of 2,2,2-trifluoroethyl methylacrylate(TFEMA) and styrene(St) were synthesized using reversible addition-fragmentation chain transfer(RAFT) polymerization in 1,4-dioxane solution,using S-1-dodecyl-S′-(α-methyl-α′-acetic acid)trithiocarbonate as the RAFT agent and 2,2′-azobisisobutyronitrile(AIBN) as initiator.The RAFT polymerization kinetics under different reaction conditions was discussed in detail.The molecular weight and chemical structure of P(TFEMA-co-St) were characterized by GPC and FTIR,respectively.The surface property and micro-topography of P(TFEMA-co-St) films were measured by contact angle method and AFM.The relatively suitable polymerization conditions were that the ratio value of [TFEMA]/[St]/[RAFT]/[AIBN]was 200∶200 ∶2∶1,and the polymerization temperature was 75℃.The results of copolymerization kinetics showed that the copolymerization was"living" and controllable.The activation energy of this polymerization was 36.49 kJ /mol.Plots of Mn versus conversion were linear.PDI of P(St-co-TFEMA) was between 1.2 and 1.4.FTIR and 1H-NMR results proved that P(TFEMA-co-St) were obtained,and that the copolymer chain showed a gradient-chain-structure character.The P(TFEMA-co-St) films had high water contact angles and relatively low surface energy,showing fluoropolymer’s characters.The micro-phase separation structure was observed in P(TFEMA-co-St) films.
关 键 词:可逆加成-断裂链转移自由基聚合 含氟共聚物 制备
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:18.188.99.196