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Studies of arenediazonium salts as a new class of electropolymerization initiator
Author(s) -
Zhang Xu,
Bell James P.
Publication year - 1999
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/(sici)1097-4628(19990912)73:11<2265::aid-app24>3.0.co;2-j
Subject(s) - potassium persulfate , ammonium persulfate , cyclic voltammetry , polymer chemistry , acrylonitrile , diazonium compounds , materials science , polyaniline , polymerization , chemistry , conductive polymer , electrosynthesis , copolymer , electrochemistry , polymer , organic chemistry , electrode
Electropolymerization holds great potential as a novel process for applying surface coatings onto a variety of substrates. Cathodic electropolymerization has been conducted successfully on metal substrates using initiation systems, such as sulfuric acid and potassium persulfate. However, each of these initiation systems has its own deficiency. This provided the motivation for investigating arenediazonium salts as a new class of cathodic electropolymerization initiators. Our studies found that arenediazonium salts can be easily reduced at reduction potentials lower than that of water to generate initiating free radicals. The reduction efficiency is very high. A copolymer of methyl acrylate and acrylonitrile has been polymerized onto steel surfaces using one of these salts, 4‐methyl benzenediazonium tetrafluoroborate, as initiator. Cyclic voltammetry and reflection absorption infrared spectroscopy (RAIRS) studies suggest a strong interaction exists between the initiator and the substrate, which can potentially enhance coating adhesion. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 2265–2272, 1999