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Macroporous chelating resins incorporating heterocyclic functional groups via hydrophilic poly(ethylene oxide) spacer arms. II. Adsorption properties
Author(s) -
Ji Chunnuan,
Qu Rongjun,
Xu Qiang,
Sun Changmei,
Wang Chunhua,
Cheng Yucui,
Song Yanpeng
Publication year - 2008
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/app.29217
Subject(s) - adsorption , ethylene oxide , polymer chemistry , chemistry , polystyrene , divinylbenzene , oxide , chelation , copolymer , polymer , nuclear chemistry , materials science , organic chemistry , styrene
Abstract Several new chelating resins prepared from macroporous chloromethylated polystyrene‐ co ‐divinylbenzene by either direct attachment of the heterocyclic functional groups, such as 2‐aminopyridine, 2‐amino‐5‐methylthio‐1,3,4‐thiadizole, 2‐amino‐5‐ethyl‐1,3,4‐thiadizole, and 2‐mercaptobenzothiazole, to the polymeric matrix or through different hydrophilic spacer arms were tested for the adsorption properties toward Hg 2+ , Ag + , Cd 2+ , and Pb 2+ in an ammonium acetate buffer solution of pH 3.0. The results show that these resins exhibited a high affinity for Hg 2+ and Ag + . The introduction of hydrophilic spacer arms between the polymeric matrix and heterocyclic functional groups resulted in an increase in the hydrophilicity and adsorption capacity of the resins. The presence of spacer arms made the kinetics of adsorption faster. The influence of the length of the spacer arm on the adsorption properties was also investigated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009