Experimental Techniques and MethodsDetermination of Triclosan and Triclocarban in Water Samples by High performance Liquid Chromatography with Dispersive Liquid-Liquid Microextraction Based on Vortex assisted Solidification of Floating Deep Eutectic Solvent
陈梦轩, 吴友谊, 周韫璐, 许梦琪. Experimental Techniques and MethodsDetermination of Triclosan and Triclocarban in Water Samples by High performance Liquid Chromatography with Dispersive Liquid-Liquid Microextraction Based on Vortex assisted Solidification of Floating Deep Eutectic Solvent[J]. 2020, 39(4): 507-513.
陈梦轩, 吴友谊, 周韫璐, 许梦琪. Experimental Techniques and MethodsDetermination of Triclosan and Triclocarban in Water Samples by High performance Liquid Chromatography with Dispersive Liquid-Liquid Microextraction Based on Vortex assisted Solidification of Floating Deep Eutectic Solvent[J]. 2020, 39(4): 507-513.DOI: doi:10.3969/j.issn.1004-4957.2020.04.012.
A novel high performance liquid chromatography(HPLC) with dispersive liquid-liquid microextraction based on vortex assisted solidification of floating deep eutectic solvent(VA-DLLME-SFDES) was established for the determination of triclosan and triclocarban in water samples.Six hydrophobic deep eutectic solvents(DESs) were newly synthesized
which physical and chemical constants such as density
melting point and octanol-water partition coefficient(KOW) were determined.One of the low density DES with suitable freezing point was selected as the micro-extractant.After vortex assisted extraction and freezing
the extractant was solidified and attached to the inner wall of the centrifuge tube.After removing the aqueous phase
the DES was melted and centrifuged in room temperature
and followed by HPLC analysis.The optimum extraction conditions were as follows:DES prepared with menthol-1 dodecanol(1∶2
molar ratio) as extraction solvent
volume of extraction solvent:70 μL
pH of water sample:5.0
vortex time:1 min.Under the optimum conditions
there were good linearities for triclosan and triclocarban in the concentration ranges of 0.59-100 μg/L and 0.26-100 μg/L
respectively
with their correlation coefficients(r2) of 0.999 8 and limits of detection(S/N=3) of 0.08-0.18 μg/L.The enrichment factors for the analytes varied from 141 to 148.Meanwhile
the recoveries were in the range of 86.0%-115% with intra-precision(n=6) and inter-precision(n=6) not more than 5.4%.The method is simple
rapid and easy in collecting the extraction phase
and it is suitable for the determination of triclosan and triclocarban in water.