Alternatively for mipdatabase quick searches go here

Custom Search

Abstract: Molecularly imprinted hybrids (MIHs) were prepared by imprinting bisphenol A (BPA) molecules with linear polystyrene-co-methyl methacrylate chains followed by anchoring SiO2 clusters onto the imprinted organic moieties. While the interior copolymer was responsible for BPA rebinding, the external SiO2 layer confined the conformation of the copolymer, suppressed the nonspecific hydrophobic interactions, and enhanced the water compatibility of copolymer. Styrene and methyl methacrylate (MMA) were used as the dual functional monomers to interact with the BPA templates via π-π stacking interaction and formation of hydrophobic backbones, respectively. The optimal composition molar ratio of BPA/styrene/MMA/3-methacryloxylpropyltrimethoxysilane/tetraethyl orthosilicate with respect to the most satisfied adsorption ability was 1/2/5/5/15. The resulting MIH compound exhibited a superior adsorption performance, including a high imprinting factor of 14, a high adsorption capacity of 40.3 mg/g, a large association constant of 3.8 × 10^4 M-1, a short equilibrium time of 20 min, and high selectivity factors of 2-24 for BPA target over the other three endocrine-disrupting chemicals according to their sizes and geometries
Template and target information: bisphenol A, BPA
Author keywords: molecular imprinting, organic-inorganic hybrid, BPA adsorption, Imprinting factor, selectivity