Journal
EUROPEAN POLYMER JOURNAL
Volume 110, Issue -, Pages 1-8Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eurpolymj.2018.10.045
Keywords
Macrocyclic ligands; Molecular imprinting; Nucleophilic attacking hydrolysis; Nanocapsule; Organophosphate pesticide catalysis degradation
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Funding
- Doctoral Fund of Ministry of Education of China (RFDP) [20130031110012]
- National Natural Science Foundation of China [50978138]
- NFFTBS [J1103306]
- PCSIRT [IRT1257]
- Fundamental Research Funds for the Central Universities
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In this work, macro cyclic amine type of functional monomers, (4-vinylbenzyl)-1,4,7-triazacyclononane (VBTN) and 1,4-bishydroxyethyl-7-(4-vinylbenzyl)-1,4,7-triazacyclononane (VBTNOH), were synthesized to prepare enzyme-mimic molecular imprinting polymers (MIPs) nanoparticles with the hollowed morphology, which are expected to eliminate organophosphorus pesticide pollutants. The resulted MIPs show higher catalytic hydrolysis activity compared to the self-hydrolysis of substrate methyl parathion. Especially, the mu) with functional monomer containing alcohol assistant group (MIP-VBTNOH), shows the best performance, whose initial rate is 3.51 * 10(-2) mM/h, 415-fold higher than substrate self-hydrolysis. Its Michaelis-Menten constant is as low as 0.87 mM. We attribute the good performance of MIP-VBTNOH to its alcohol assistant group on the funcional monomers because the alcohol OH is more nucleophilic than water. Such mechanism is confirmed by the observation of the intermediate in this catalytic process by P-31 NMR spectrum. In addition, the introduce of hollowed nanocapsule morphology makes MIPs effectively absorb p-nitrophenol produced by the hydrolysis of organophosphate compounds, another pollutant needs to be eliminated.
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