Multifunctional polymeric microspheres were prepared using hyper-cross-linking chemistry combined with surface-initiated atom transfer radical polymerization. The synthesized microspheres exhibited good water dispersibility, a high surface area, and pH/thermo dual-responsiveness. Fluoroquinolones (FQs), which contains a hydrophilic piperazine ring and hydrophobic fluorine atoms, were used as target analytes to assess the performance of the microspheres as a sorbent for dispersive solid-phase extraction (d-SPE). The d-SPE experimental parameters, including extraction time, amount of microspheres, extraction temperature, and sample solution pH, as well as the desorption conditions, were systematically studied. Coupled with LCMS/MS, an analytical method for analysis of trace-level FQs in water samples was developed and validated. Under optimal conditions, linearity with correlation coefficients (r) of >0.99 was achieved in the concentration range of 0.02–10 μg L−1. The limits of detection and quantification for the selected FQs were 5.0–6.7 and 12–20 ng L−1, respectively. High recovery values (93.1%–97.2%), a high enrichment factor (˜180), and good precision (RSD < 8%, n = 6) were obtained for FQ determination in spiked purified water samples. It was proposed that hydrophilic–hydrophobic transition induced by stretching and shrinking of polymer chains under different pH and temperature conditions offered good control of the surface wettability and altered the extraction behavior. The developed method was validated and was successfully applied to the analysis of FQs in environmental water samples, meat and milk samples. These results demonstrated that the water-dispersible polymeric microspheres have good potential for use in separation and extraction techniques.

A solid-phase extraction method using Pb²⁺ion-imprinted polymer (Pb²⁺-IIP) nanoparticles combined with flame atomic absorption spectrophotometry (FAAS) was developed for the preconcentration and trace monitoring of lead ions in environmental samples. The Pb²⁺-IIP nanoparticles were obtained by precipitation polymerization of 4-vinylpyridine (the functional monomer), ethylene glycol dimethacrylate (the cross-linker), 2,2′-azobisisobutyronitrile (the initiator), 4-(2-pyridylazo) resorcinol (the lead-binding ligand), and lead ions (the template ion) in acetonitrile solution. The Pb²⁺-IIP nanoparticles were characterized by Fourier transformed infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric and differential thermal analysis (TGA/DTA), and by scanning electron microscopy (SEM). Different affecting parameters on the adsorption and desorption of this solid-phase extraction process were evaluated and optimized. Under the optimized conditions, the detection limit for the proposed method was found to be 0.9 μg L⁻¹, while the relative standard deviation (RSD) for five replicate measurements was calculated to be <4 %. For proving that the proposed method is reliable, a range of food and water samples with different and complex matrices was used.

We describe a nanosized Hg(II)-imprinted polymer that was prepared from methacrylic acid as functional monomer, ethyleneglycol dimethacrylate as cross-linker, 2,2′-azobisisobutyronitrile (AIBN) as radical initiator, 2, 2′-di pyrydyl amine as a specific ligand, and Hg (II) as the template ions by precipitation polymerization method in methanol as the progeny solvent. Batch adsorption experiments were carried out as a function of pH, Hg (II) imprinted polymer amount, adsorption and desorption time, volume, and concentration of eluent. The synthesized polymer particles were characterized physically and morphologically by using infrared spectroscopy, thermogravimetric analysis, X-ray diffraction, and scanning electron microscopic techniques. The maximum adsorption capacity of the ion-imprinted and non-imprinted sorbent was 27.96 and 7.89 mg g⁻¹, respectively. Under optimal conditions, the detection limit for mercury was 0.01 μg L⁻¹ and the relative standard deviation was 3.2 % (n = 6) at the 1.00 μg L⁻¹. The procedure was applied to determination of mercury in fish and water samples with satisfactory results.

In this paper, we describe ultrasonic assisted-dispersive solid phase extraction based on ion-imprinted polymer (UA-DSPE-IIP) nanoparticles for the selective extraction of lead ions. Ultrasound is a good and robust method to facilitate the extraction of the target ions in the sorption step and elution of the target ions in the desorption step. The ion-imprinted polymer nanoparticles used in the UA-DSPE-IIP were prepared by precipitation polymerization technique. The ion-imprinted polymer nanoparticles was synthesized using 2-vinylpyridine as a functional monomer, ethylene glycol dimethacrylate as the cross-linker, 2,2′- azobisisobutyronitrile as the initiator, 1,3,4-thiadiazole-2,5-dithiol as the ligand, methanol/dimethyl sulfoxide as the solvent, and lead as the template ion, through precipitation polymerization technique. The IIP nanoparticles were characterized by Fourier transformed infra-red spectroscopy (FTIR), thermogravimetric and differential thermal analysis (TGA/DTA), and scanning electron microscopy (SEM). Box-Behnken design (BBD) was used for optimization of sorption and desorption steps in UA-DSPE-IIP. In the sorption step: pH of solution, IIP amount (mg), sonication time (min) for sorption and in the desorption step: concentration of eluent (mol L⁻¹), volume of eluent (mL), and sonication time (s) for desorption was investigated and optimized by the Box-Behnken design. The optimum conditions for the method were pH of solution: 7.5, sonication time for sorption 7.5 min, IIP amount 24 mg, type and concentration of eluent HCl 1.4 mol L⁻¹, volume of eluent 2.1 mL, and sonication time for desorption 135 s. Under the optimized conditions, the limit of detection and relative standard deviation for the detection of lead ions by UA-DSPE-IIP was found to be 0.7 μg L⁻¹ and <4%, respectively.