Molecularly imprinting technique was combined with magnetic nanoparticles to synthesize molecularly imprinted polymer‐encapsulated particles for selective removal and efficient separation of estrogenic compounds from water. The core‐shell‐structured particles were successfully prepared by a novel 2‐h ultrasonication‐assisted synthesis in a mixture of water and organic solvent using dual‐layer surfactant‐modified magnetic particles as core, the most physiologically active estrogenic compound (17β‐estradiol) as template, and widely adapted methacrylic acid as functional monomer. Ultraviolet–visible spectroscopy, Fourier transform infrared spectroscopy, scanning electron microscopy, and magnetic separation were used to characterize the particles. High‐performance liquid chromatography–tandem mass spectrometry was used for quantitative binding performance analysis at low‐nanogram per milliliter levels. The particles exhibited satisfactory recognition of 17β‐estradiol in water. They possessed great potential for rapid, cost‐effective, and efficient separation of estrogenic compounds from aqueous environment with specificity. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers

The removal of steroid and phenolic endocrine-disrupting compounds (EDCs) from an aqueous environment was investigated using magnetic particles encapsulated by a duo-molecularly imprinted polymer (duo-MIP). The effect of environmental variables on the binding efficiency was studied. Experimental results showed that the amount of EDCs adsorbed was neither affected by up to 10.0 mM NaCl nor significantly interfered by up to 10.0 mg/L humic acid. Negligible influence was observed from pH 3.3 to pH 6.8, but a decrease started at pH 9. Freundlich isotherm parameters indicated binding capacities in the order of DES > E2 ∼ E1 > BPA. The applicability of class-selective removal was verified using river water samples spiked with these EDCs at 10 μg/L; the binding efficiencies were 90, 90, 88, and 98 % for estrone (E1), 17β-estradiol (E2), bisphenol A (BPA), and diethylstilbestrol (DES), respectively. A reuse investigation verified constant binding capacities exhibiting <2 % reduction after seven cycles of regeneration.

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