The immobilized metal
affinity cryogels based on poly(2-hydroxyethyl
methacrylate-co-glycidyl methacrylate) (p(HEMA-GMA))
containing hydroxy and epoxy groups were prepared by free-radical
copolymerization under cryogenic condition and then functionalized
with iminodiacetic acid and chelated Cu2+, Ca2+, and Fe3+ ions to the p(HEMA-GMA) cryogel. The structures
of p(HEMA-GMA) and immobilized metal-affinity cryogels were analyzed
by Fourier transform infrared spectroscopy and scanning electron microscopy
(SEM)–energy dispersive X-ray spectroscopy. SEM results showed
that the prepared cryogels had interconnected pores with the size
of 30–100 μm. The performance of water swelling into
the cryogels was fitted in Fickian diffusion. The adsorption property
of cryogels was influenced by the immobilized ionic type, temperature,
and adsorbate. The adsorption capacity of immobilized Cu2+ cryogel (p(HEMA)–Cu2+ (0.5 M) cryogel) was the
highest in comparison with that of Ca2+ and Fe3+ affinity cryogels under the same condition. The maximum adsorption
capacity of p(HEMA)–Cu2+ (0.5 M) cryogel for porcine
pancreatic lipase was 150.14 mg/g at a higher temperature of 35 °C,
whereas for bovine serum albumin, the maximum adsorption capacity
was 154.11 mg/g at a lower temperature of 25 °C. The research
of thermodynamics and kinetics indicated that the mechanism of the
protein adsorption process corresponded to the Langmuir model and
pseudo-second-order model.