Abstract

A novel macroporous magnetic molecularly imprinted polymer (MMIPs) of was prepared by W/O Pickering (high internal phase emulsions) HIPEs polymerization, and then it was adopted as adsorbent for selective adsorption of λ-cyhalothrin (LC). In static conditions, adsorption capacity of LC increased rapidly in the first 60 min and reached to equilibrium in ~2.0 h. Excellent conformity of the second-order model confirmed the chemical nature of the interaction between the LC and imprinted sites. The fitting adsorption isotherm was a Langmuir type, and the maximum monolayer adsorption capacity at 298 K was 404.4 μmol g−1. Thermodynamic parameters suggested the specific adsorption at 298 K was an exothermic, spontaneous, and entropy decreased process. Competitive recognition studies of the MMIPs were performed with diethyl phthalate (DEP) and the structurally similar compound fenvalerate (FL), and the MMIPs, which displayed high selectivity for LC.

Highlights

  • In recent years, pyrethroids are high effective insecticide widely used in agriculture, such as fishery, vegetables, forestry, and grain (Ye et al, 2015)

  • The polymerization of Pickering High internal phase emulsions (HIPEs) templates with the internal phase volume of 75, 80, 85, 90%, respectively, resulted in magnetic MIPs (MMIPs) 1–4 (Table 1), which have many larger pores and pore throats (Figures 2a–d)

  • The heterogeneity of pore is observed in typical structure of MMIPs 1, 2, 3, while MMIPs 4 resulted from

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Summary

Introduction

Pyrethroids are high effective insecticide widely used in agriculture, such as fishery, vegetables, forestry, and grain (Ye et al, 2015). They can be inadvertently released into the environment, resulted in contaminating rivers and ground waters. It is necessary to develop an efficient and rapid method to remove the pyrethroids released into our environment even if in the form of trace amount in water samples. Imprinted polymers (MIPs) as a versatile technology contain highly cross-linked polymer matrix with template molecules. After the template is eluted, recognition sites in synthetic polymers exhibit a high selectivity for rebinding the target molecules and the similar structures (Chen et al, 2015; Randa et al, 2015). There are several studies focused on the MIPs as novel adsorbent for specific removal of antimicrobial drugs, phenols, and heavy metal ions (Pan et al, 2012; Dolak et al, 2015; Zamora-Gálvez et al, 2016)

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