Abstract

AbstractAtom 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 ± 3°C; 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 diethanolamine, 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 50°, significantly increasing the hydrophilicity of the film surface. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1589–1595, 2004

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