Abstract

Personal care product (PCP) residues - classified under micropollutants (MPs)- are widely found in aquatic environments, posing trace-level toxicity. Traditional water treatment techniques struggle to remove these toxins effectively. Deep eutectic solvents (DESs), the liquid mixtures typically composed of hydrogen bond donors (HBDs) and hydrogen bond acceptors (HBAs), have recently emerged as a viable alternative for extracting pollutants from water. Among DESs, hydrophobic deep eutectic solvents (HDESs) exhibit low water miscibility and unique solvent properties. The main objective of this study is to synthesize HDESs to effectively eliminate 2-naphthol and methylparaben- two of the significant chemical contaminants in PCPs- from aqueous media. HDESs were prepared by mixing different terpenes (menthol and thymol) and long-chain carboxylic acids at varying molar ratios. They were characterized using different spectroscopic and thermal techniques. The density and viscosity of the pure DESs were measured as afunction of temperature. Experimental studies were carried out using the liquid–liquid extraction (LLE) method, and the factors influencing the efficiency of extraction were optimized.Considering the limited number of studies on the extraction mechanism of MPs from aqueous media, this study employs comprehensive computational methods, including density functional theory (DFT) and the COnductor-like Screening MOdel for Real Solvents (COSMO-RS), to provide a detailed interpretation of the extraction mechanism. A series of successive extractions were conducted to reduce the DES usage to ensure economic viability. The reusability of the best-performed DES was explored. Additionally, the regeneration of one of the DESs was accomplished through activated carbon-based recovery.---------------------------------------------------------------------------------------------------------------------

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