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Updated: May 8, 2026

Microwave-assisted Functionalization of Poly(ethylene glycol) and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
Published on: October 29, 2013
Characterization and bisphenol A adsorption capacity of β-cyclodextrin-carboxymethylcellulose-based hydrogels
Hiroyuki Kono1, Kenta Onishi, Taichi Nakamura
1Department of Science and Engineering for Materials, Tomakomai National College of Technology, Nishikioka 443, Tomakomai, Hokkaido 059-1275, Japan. kono@sem.tomakomai-ct.ac.jp
Abstract:
Novel hydrogel beads having molecular adsorption abilities were prepared from carboxymethylcellulose sodium salt (CMC) and β-cyclodextrin (β-CD) by suspension crosslinking, using ethylene glycol diglycidyl ether (EGDE) in basic medium as a crosslinking agent. FTIR and solid-state NMR spectroscopic analysis revealed that the amount of incorporated β-CD and crosslinking densities within the hydrogel bead structures are strongly dependent on the molar feed ratio of β-CD to CMC during preparation. The hydrogel beads showed water-swelling capacities of 70-200 mL/g-polymer, with decreases in capacity associated with increased amounts of β-CD incorporated in the gel structure. The hydrogel beads also showed a high adsorption capacity toward bisphenol A (BPA) in water. Batch BPA-adsorption experiments were analyzed employing Langmuir isotherm models; hydrogel bead adsorption isotherms for BPA could be fitted to the Langmuir model. The maximum BPA-adsorption among the prepared series of hydrogel beads amounted to 167 μmol g(-1).

