Surface grafting of polyacrylamide from polyethylene-based copolymer film

被引:22
|
作者
Luo, N
Husson, SM [1 ]
Hirt, DE
Schwark, DW
机构
[1] Clemson Univ, Dept Chem Engn, Clemson, SC 29634 USA
[2] Clemson Univ, Ctr Adv Engn Fibers & Films, Clemson, SC 29634 USA
[3] Cryovac Div Sealed Air Corp, Duncan, SC 29334 USA
关键词
polyethylene (PE); functionalization of polymers; surfaces; atom transfer radical polymerization (ATRP); hydrophilic polymers;
D O I
10.1002/app.20103
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Atom transfer radical polymerization (ATRP) was used to grow polyacrylamide from the surface of ethylene-acrylic acid copolymer (EAA) film. The surface functionalization constituted initiator immobilization and surface graft polymerization. All reaction steps were conducted at 24 +/- 3degreesC; polymerization was done in aqueous solution. For initiator immobilization, the carboxylic acid groups on EAA film were converted to acid chloride groups; further reaction with ethanolamines gave hydroxyl groups onto which 2-bromoisobutyryl bromide initiator was attached. ATR-FTIR data indicated that 1.64 +/- 0.09 times higher initiator density was achieved by using diethanol-amine, relative to ethanolamine. Acrylamide monomer was polymerized from the initiator by ATRP to yield nondistorted, transparent films with polymerization times of up to 1 h. For films prepared using diethanolamine, 1 h polymerization time reduced the static water contact angle by more than 50degrees, significantly increasing the hydrophilicity of the film surface. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:1589 / 1595
页数:7
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