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The effect of crosslinking on the adsorption behavior of copper (II) onto poly(2‐hydroxy‐4‐acryloyloxybenzophenone)
Author(s) -
Zalloum Hiba M.,
ElEswed Bassam,
Zalloum Ruba M.,
Mubarak Mohammad S.
Publication year - 2012
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.36996
Subject(s) - adsorption , polymer , copper , langmuir adsorption model , aqueous solution , metal ions in aqueous solution , ionic strength , isothermal process , chelation , chemistry , divinylbenzene , kinetics , polymer chemistry , ion , inorganic chemistry , perchlorate , materials science , organic chemistry , copolymer , styrene , physics , thermodynamics , quantum mechanics
The adsorption behavior of Cu(II) ions onto poly(2‐hydroxy‐4‐acryloyloxybenzophenone), polymer I, and onto poly(2‐hydroxy‐4‐acryloyloxybenzophenone) crosslinked with different amounts of divinylbenzene (DVB), polymers II, III, and IV, in aqueous solutions was investigated using batch adsorption experiments as a function of contact time, pH, and temperature. The amount of metal ion uptake of the polymers was determined by using atomic absorption spectrometry (AAS) and the highest uptake was achieved at pH 7.0 and by using perchlorate as an ionic strength adjuster for polymers I, II, III, and IV. Results revealed that the adsorption capacity ( q e and Q m ) of Cu(II) ions decreases with increasing crosslinking due to the decrease of chelation sites. In addition, the rate of adsorption ( k 2 ) of Cu(II) ions decreases with the increase of crosslinking because it becomes more difficult for Cu(II) ions to diffuse into the chelation sites. The isothermal behavior and the kinetics of adsorption of Cu(II) ions on these polymers with respect to the initial mass of the polymer and temperature were also investigated. The experimental data of the adsorption process was found to correlate well with the Langmuir isotherm model. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

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