Deep eutectic solvent based homogeneous liquid–liquid extraction coupled with in‐syringe dispersive liquid–liquid microextraction performed in narrow tube; application in extraction and preconcentration of some herbicides from tea

2019 ◽  
Vol 42 (9) ◽  
pp. 1768-1776 ◽  
Author(s):  
Mohammadali Torbati ◽  
Mir Ali Farajzadeh ◽  
Mohammad Reza Afshar Mogaddam ◽  
Mostafa Torbati
2020 ◽  
Vol 12 (34) ◽  
pp. 4220-4228
Author(s):  
Ali Saei ◽  
Afshin Javadi ◽  
Mohammad Reza Afshar Mogaddam ◽  
Hamid Mirzaei ◽  
Mahboob Nemati

A combination of homogeneous liquid–liquid extraction and dispersive liquid–liquid microextraction based on solidification of a deep eutectic solvent is used for the extraction of 3 widely used antibiotics (oxytetracycline, penicillin G and tilmicosin) from sausage samples.


RSC Advances ◽  
2015 ◽  
Vol 5 (95) ◽  
pp. 77501-77507 ◽  
Author(s):  
Mir Ali Farajzadeh ◽  
Mohammad Reza Afshar Mogaddam ◽  
Ali Akbar Alizadeh

Development of a new version of homogeneous liquid–liquid extraction based on water induced followed by dispersive liquid–liquid microextraction for extraction of neonicotinoid insecticides from oil samples.


2020 ◽  

<p>This paper presents an efficient, simple, and fast method for the derivatization, extraction, and preconcentration of several phenolic compounds (phenol, o–, m– and p–cresol, 4–chlorophenol, and 2–nitrophenol) from wastewater samples and analysis of those samples by gas chromatography–flame ionization detection. In this method, initially the phenolic compounds are derivatized with acetic anhydride in an alkaline pH. In the following, the derivatized analytes are extracted into mL–volume of acetonitrile during homogeneous liquid–liquid extraction and further enrichment of the analytes are accomplished by their extraction into µL–volume of 1,1,2–trichloroethane through dispersive liquid–liquid microextraction step. Effective parameters controlling the performance of the proposed method such as type and volume of derivatization agent and catalyst, type and volume of extraction/disperser solvent in homogeneous liquid–liquid extraction, and type and volume of extraction solvent and salt addition in dispersive liquid–liquid microextraction are optimized. Under optimum conditions linear range of the proposed method was obtained 0.7–4000 µg L–1. Limits of detection and quantification were in the ranges of 0.07–0.20 and 0.23–0.70 µg L–1, respectively. Enrichment factors and extraction recoveries were ranged from 220 to 440 and 44 to 88%, respectively.</p>


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