Studies of Imprinting Conditions and Application Performance of Pirimicarb Molecule-Imprinted Material Prepared Using a Novel Surface-Imprinting Technique

摘要

Methacrylic acid (MAA) was graft-polymerized on to the surface of silica gel particles in the “grafting from” manner, resulting in grafted PMAA/SiO₂ particles. By adopting the novel surface molecular imprinting technique proposed by us not long ago, pirimicarb molecule-imprinted material MIP-PMAA/SiO₂ was prepared with ethylene glycol diglycidyl ether (EGGE) as crosslinking agent. The effects of imprinting conditions, for example pH of the medium, solvent composition, and reactant ratio, on the recognition selectivity of MIP-PMAA/SiO₂ for pirimicarb relative to the analog, propoxur, were examined, and the optimum imprinting conditions were determined. The dependence of the rebinding ability of MIP-PMAA/SiO₂ for pirimicarb on the performance conditions, for example pH and salinity of the medium, were also studied. The experimental results showed that optimum imprinting conditions for preparing pirimicarb molecule-imprinted MIP-PMAA/SiO₂ material with high recognition selectivity were: solvent pH 8, mixed solvent composition 1:1 (v/v) ethanol to water, and 3:1 reactant molar ratio of carboxyl groups of the grafted PMAA to the crosslinking agent EGGE. This reactant ratio is consistent with the speculated mode of intermolecular interaction between the grafted functional macromolecule PMAA and the template pirimicarb. The rebinding ability of MIP-PMAA/SiO₂ for pirimicarb is highly dependent on the performance conditions. At medium pH 8, MIP-PMAA/SiO₂ has the strongest binding ability for pirimicarb because this condition results in the greatest the number of active sites inside the imprinted cavities suitable for the binding of pirimicarb. A saline, i.e., high ionic strength, medium is disadvantageous to rebinding ability of MIP-PMAA/SiO₂ for pirimicarb. Keywords Surface molecular imprinting - Poly(methacrylic acid) - Pirimicarb - Silica gel particle - Recognition selectivity