The features and nature of the sorptive phase may be the stage that determines the scope of microextraction techniques. In search of new alternatives, materials of natural origin have recently been explored to establish greener analytical strategies. Based on that search, this research proposes the use of chitosan as a sorptive phase, which was assessed in the rotating disk sorptive extraction of emerging contaminants from aqueous systems. Chitosan is a biopolymer of animal origin that is usually found in the shells of crustaceans. The main characteristic of this material is the presence of a high number of nitrogenous groups, which gives it high reactivity, but its main disadvantage is associated with its high swelling capacity. In this research, chitosan was crosslinked with a low concentration of glutaraldehyde to form thin films that were easily immobilized on the surface of the rotating disk. The main advantage of this modification is the considerable decrease in the swelling capacity, which prevents loss and rupture of the sorbent during high rotation of the disk. In addition, it not only improved the physical characteristics of chitosan but also increased its extraction capacity. With regard to its use as a sorptive phase, all the variables associated with the microextraction of the analytes were studied, and optimal variables were found to be: pH 4, 20% NaCl (salting out effect), 30-45 min as equilibrium time and elution of analytes with a mixture of methanol:ethyl acetate (1:1). Validation of the methodology for the determination of methyl triclosan and triclosan was carried out, and relative recoveries between 89 and 96% and relative standard deviations less than 14% were found. The detection limits were 0.11 and 0.20 μg L, respectively. Through its application in real samples (natural and residual waters), triclosan was quantified between 0.7 and 1.3 μg L. Finally, the "green" properties of the phase were evaluated, demonstrating that it is reusable for at least three cycles and biodegradable. Compared to its efficiency with a commercial phase (in this case, the styrene divinyl benzene phase), the proposed biosorbent provided a similar and even higher sorptive capacity (depending on the analyte).
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http://dx.doi.org/10.1016/j.aca.2023.341053 | DOI Listing |
Talanta
December 2024
College of Chemistry, Liaoning University, Shenyang, 110036, China. Electronic address:
The development of a novel multifunctional adsorbent for the sensitive detection and capture of antibiotic residues in environmental and food samples presents a significant challenge. In this study, we synthesized a pioneering nanocomposite, ILs@PC, by encapsulating task-specific ionic liquids (ILs) within nitrogen-doped porous carbon (PC) derived from metal-triazolate frameworks. This ILs@PC nanocomposite functions as a multifunctional adsorbent in dispersive solid-phase extraction (DSPE), enabling simultaneous sorptive removal, sensitive detection, and molecular sieve selection.
View Article and Find Full Text PDFMolecules
November 2024
Institute for Nanotechnology and Water Sustainability, College of Science, Engineering, and Technology, University of South Africa, Florida Science Campus, Roodepoort 1710, South Africa.
Due to their antibacterial and antifungal properties, parabens are commonly used as biocides and preservatives in food, cosmetics, and pharmaceuticals. Parabens have been reported to exist in various water matrices at low concentrations, which renders the need for sample preparation before their quantification using analytical techniques. Thus, sample preparation methods such as solid-phase extraction (SPE), rotating-disk sorptive extraction (RDSE), and vortex-assisted dispersive liquid-liquid extraction (VA-DLLE) that are commonly used for parabens extraction and preconcentration have been discussed.
View Article and Find Full Text PDFAnal Bioanal Chem
January 2025
GICAPC Research Group, Department of Analytical Chemistry, University of Valencia, 46100, Burjassot, Valencia, Spain.
In this work, a miniaturized and sustainable method for the determination of endocrine-disrupting bisphenols in human serum and urine employing the miniaturized stir bar sorptive dispersive microextraction (mSBSDME) approach has been developed. As bisphenols are conjugated in the human body to their glucorinated and sulfated forms, an enzymolysis employing a commercial mixture of β-glucuronidase and arylsulfatase was carried out prior to the microextraction procedure to determine their total content. A magnetic covalent organic framework (COF) was employed as the sorbent to carry out the extraction of the analytes from the biological matrixes, showing good extraction performance due to its hydrophobic, π-π, and dipole-dipole interactions with the analytes.
View Article and Find Full Text PDFSci Total Environ
December 2024
Department of Geosciences, University of Cincinnati, Cincinnati, OH, USA; Department of Chemical and Environmental Engineering, University of Cincinnati, Cincinnati, OH, USA. Electronic address:
Molecules
October 2024
Faculty of Food Science and Nutrition, Poznań University of Life Sciences, Wojska Polskiego 31, 60-624 Poznań, Poland.
The coupling of Solid-Phase Microextraction (SPME) technology with gas chromatography (GC) has a well-established and successful history. Traditionally, SPME fibers have been the most popular form thanks to their versatility and the ease with which they can be fully automated. However, alternative geometries for SPME have been developed over the years, beginning with Stir Bar Sorptive Extraction (SBSE) and later evolving into Thin-Film SPME (TF-SPME) devices.
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