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- W4387131502 abstract "Abstract An environmental friendly ferrofluid incorporating hydrophobic deep eutectic solvents derived from fatty acids, specifically caprylic acid, pelargonic acid, capric acid, and lauric acid have been developed. The fundamental physiochemical properties of the synthesised deep eutectic solvents ferrofluid were determined using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), and scanning electron microscopy (SEM). Later, they will be used as alternative adsorbents in ferrofluid liquid-phase microextraction. Five polycyclic aromatic hydrocarbons (PAHs) were determined simultaneously using gas chromatography with a flame ionisation detector. The most important extraction parameters were optimised, and the procedure was validated. The selected experimental variables were then optimised using Box-Behnken design (BBD). The developed method is also assessed by Analytical Eco-Scale and Analytical Greenness for greenness method evaluation. Under the optimal conditions, the presented method demonstrated wide linear ranges of 0.005–5 µg mL − 1 for all PAHs. The limit of detections (LODs) and quantifications (LOQs) of PAHs varied from 0.4–1.70 ng mL − 1 and 1.33–5.67 ng mL − 1 , respectively. The extraction recoveries of spiked samples for FF-LPME ranged from 75.78 to 118.65% with RSD < 15%. The Analytical Eco-scale and Analytical GREENness Metric Approach System (AGREE) measured 92% and 0.64, respectively. The optimised process successfully delivered an environmentally friendly adsorbent, demonstrating a highly promising approach for extracting PAHs from various environmental samples." @default.
- W4387131502 created "2023-09-29" @default.
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- W4387131502 date "2023-09-28" @default.
- W4387131502 modified "2023-10-18" @default.
- W4387131502 title "Low Toxicity Liquid Phase Microextraction Using Deep Eutectic Solvent-Based Ferrofluid for Enrichment Polycyclic Aromatic Hydrocarbon in Environmental Samples" @default.
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- W4387131502 doi "https://doi.org/10.21203/rs.3.rs-3291056/v1" @default.
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