In this work, a novel approach was developed to perform dispersive liquid-liquid microextraction using a rapid pressure variation to disperse the extraction solvent in an aqueous medium. A glass syringe was used to produce an environment subject to a rapid pressure difference. The element used as a model was nickel and the approach was called pressure variation in-syringe dispersive liquid-liquid microextraction (PV-IS-DLLME). The extraction solvent used was 1-butyl-3-methylimidazolium hexafluorophosphate, and ammonium pyrrolidine dithiocarbamate was the complexing reagent. The variables pH, solvent volume, amount of complexing agent, extraction time and syringe volume were studied by a factorial 2 fractional design. All variables were significant. However, the two least significant, amount of complexing agent (50.0 μL) and syringe volume (20.0 mL) were fixed at their optimum levels, according to the generated Pareto chart. A Doehlert matrix was studied for the variables volume of solvent, pH and extraction time to obtain optimal levels of these factors, and the contour plots showed the following critical values: 120.0 μL, 2.0 and 60.0 s respectively. The developed method presented limits of detection and quantification of 0.1 and 0.3 mg kg, an enrichment factor of 17 and a precision of 4.8% (100.0 μg L). The developed method was applied to the analysis of samples of powdered chocolate and certified reference material.
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http://dx.doi.org/10.1016/j.talanta.2018.09.082 | DOI Listing |
Cell
December 2024
Schaller Research Groups, Department of Infectious Diseases, Virology, Heidelberg University, Heidelberg, Germany; BioQuant, Heidelberg University, Heidelberg, Germany. Electronic address:
J Environ Health Sci Eng
June 2025
Department of Environmental Health Engineering, School of Health, Isfahan University of Medical Sciences, Isfahan, Iran.
In the present study, two most commonly used Perfluoroalkyl substances (PFASs), namely perfluorooctanoic acid (PFOA) and perfluorooctanesulfonate (PFOS), were determined in 45 tap water samples from the city of Isfahan (Iran) by dispersive liquid-liquid extraction (DLLME) and liquid chromatography-mass spectrophotometry (LC-MS) analysis. Risk assessment was also performed to determine the risk to human health. The mean concentration of PFOA was 38.
View Article and Find Full Text PDFTalanta
December 2024
Department of Analytical Chemistry, Faculty of Chemistry, University of Murcia, Regional Campus of International Excellence "Campus Mare Nostrum", E-30100, Murcia, Spain.
A reliable and sensitive analytical platform is proposed for the assessment of pig exposure to mycotoxins through the consumption of commercial feed. A total of 48 naturally contaminated feed and 55 urine samples collected from eight Spanish farms were analyzed using a fast and simple methodology based on solid-liquid extraction (SLE) or liquid-liquid extraction (LLE) and dispersive liquid-liquid microextraction (DLLME). High-performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) was used for the targeted analysis of 27 mycotoxins from different families in both matrices achieving limits of quantification in a range of 0.
View Article and Find Full Text PDFMar Pollut Bull
December 2024
Universidade Federal de Pernambuco, Departamento de Química Fundamental, Av. Jornalista Aníbal Fernandes, s/n, Cidade Universitária, 50740-560 Recife, PE, Brazil. Electronic address:
In August 2019, Brazil experienced its largest large oil spill, which impacted extensive areas and significantly affected the northeastern region, particularly Pernambuco. Polycyclic aromatic hydrocarbons (PAHs), major oil components, are critical for assessing fish contamination risks. This study presents two sample pretreatment methods for fish samples - ultrasound-enhanced air-assisted liquid-liquid microextraction (UE-AA-LLME) for low molar mass PAHs, and matrix solid-phase dispersion for high molar mass PAHs - followed by a Gas-Chromatography coupled to Mass Spectrometry (GC-MS) detection.
View Article and Find Full Text PDFChemosphere
December 2024
Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research, 08034 Barcelona, Spain. Electronic address:
The assessment of persistence of organic pollutants in seawater is limited by the lack of user-friendly, quick protocols for assessing one of their main sinks, degradation by marine bacteria. Here we present an experimental workflow to identify organic pollutants degradation, taking organophosphate esters flame retardants and plasticizers (OPEs-FR-PL), as a model family of synthetic chemicals released into the marine environment that are particularly widespread due to their persistence and semi-volatile nature. The proposed novel workflow combines culture-dependent techniques, solvent demulsification-dispersive liquid-liquid microextraction, with quantitative liquid chromatography coupled with mass spectrometry analyses in order to identify marine bacterial isolates with the potential to degrade OPEs-FR-PL in the marine environment.
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