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Magnetic cellulose nanoparticles (MCNPs) coated with 1-butyl-3-methylimidazolium hexafluoro phosphate [C 4 MIM][PF 6 ] ionic liquid (IL) through electrostatic interactions are proposed for the first time as sorbents in a magnetic solid phase extraction (MSPE) method for the determination of paracetamol (PAR), ibuprofen (IBU), naproxen (NAP) and diclofenac (DIC) in natural waters. The parameters that affect adsorption (dispersive solvent, amount of IL, pH and salt content) and desorption (desorption solvent, type of energy and time) were studied. The values that provided the maximum adsorption efficiency and extraction recovery were selected as optimum conditions for adsorption and desorption, respectively. Under the optimum conditions, the adsorption and desorption of all analytes was simultaneous and quantitative. High performance liquid chromatography (HPLC) with ultra violet (UV) and fluorescence (FL) detector was used after the sample preparation. The precision, expressed as relative standard deviation was between 1.4 and 7.6%. Limits of detection and quantification were in the range 3.2–7.2 μg L − 1 and 11–24 μg L − 1 , respectively. Moreover, the proposed method provides enrichment factors from 29.0 to 34.2. Recovery studies on 10 mL of spiked tap, river and dam water samples at 50 and 100 μg L − 1 were carried out. The extraction recoveries were from 85 to 116%, and were in a comparable range regardless of the type of water. The method is simple, rapid, and environmentally friendly. [ABSTRACT FROM AUTHOR]

Magnetite (Fe3O4) nanoparticles were modified with nanocellulose and are showed to be a useful sorbent for magnetic solid-phase extraction of mercury species. Speciation analysis was performed by using gas chromatography coupled to atomic fluorescence detection (GC-pyro-AFS). The magnetic properties of the sorbent make this approach simple and rapid, and the use of a renewable and biodegradable nanomaterial (nanocellulose) makes it environmentally friendly. The factors that affect adsorption (pH value, amount of nanomaterial, time, volume of sample) and desorption (solvent, time) have been optimized. Both desorption and derivatization of mercury species were performed in a single step. This reduces considerably the sample preparation time. Under the optimized conditions, the limits of detection are 4.0 pg mL−1 for monomethylmercury and 5.6 pg mL−1 for inorganic mercury. The repeatability and reproducibility are satisfactory. The method enables inorganic mercury and monomethylmercury to be simultaneously extracted, with preconcentration factors up to 300. The potential interferences of organic matter and/or co-existing ions were also investigated using synthetic waters. The procedure was applied to the analysis of tap water and river water samples with different characteristics from a mercury polluted area (Almadén, Spain). The extraction recoveries ranged from 81 to 98% regardless of the type of water, which demonstrates the applicability of the method. This is the first time that this kind of sorbent is used for trace metal speciation. [ABSTRACT FROM AUTHOR]