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
Keyword(s):  
Deep Eutectic Solvent ◽  
Liquid Extraction ◽  
Narrow Tube ◽  
Homogeneous Liquid ◽  
Liquid Liquid Extraction ◽  
Dispersive Liquid Liquid Microextraction ◽  
Tube Application ◽  
Liquid Microextraction

Development of homogeneous liquid–liquid extraction combined with dispersive liquid–liquid microextraction based on solidification of floating droplets of a ternary component deep eutectic solvent for the analysis of antibiotic residues in sausage samples prior to ion mobility spectrometry

2020 ◽  
Vol 12 (34) ◽  
pp. 4220-4228
Author(s):  
Ali Saei ◽  
Afshin Javadi ◽  
Mohammad Reza Afshar Mogaddam ◽  
Hamid Mirzaei ◽  
Mahboob Nemati
Keyword(s):  
Ion Mobility ◽  
Deep Eutectic Solvent ◽  
Liquid Extraction ◽  
Penicillin G ◽  
Antibiotic Residues ◽  
Homogeneous Liquid ◽  
Liquid Liquid Extraction ◽  
Dispersive Liquid Liquid Microextraction ◽  
Ternary Component ◽  
Liquid Microextraction

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.

Determination of neonicotinoid insecticide residues in edible oils by water-induced homogeneous liquid–liquid extraction and dispersive liquid–liquid extraction followed by high performance liquid chromatography-diode array detection

RSC Advances ◽  
2015 ◽  
Vol 5 (95) ◽  
pp. 77501-77507 ◽  
Author(s):  
Mir Ali Farajzadeh ◽  
Mohammad Reza Afshar Mogaddam ◽  
Ali Akbar Alizadeh
Keyword(s):  
High Performance ◽  
Edible Oils ◽  
Liquid Extraction ◽  
Homogeneous Liquid ◽  
Liquid Liquid Extraction ◽  
Neonicotinoid Insecticide ◽  
Array Detection ◽  
Dispersive Liquid Liquid Microextraction ◽  
Liquid Microextraction

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.

scholarly journals Determination of phenolic compounds in industrial wastewaters by gas chromatography after extraction and preconcentration by microextraction procedure

2020 ◽  
Keyword(s):  
Gas Chromatography ◽  
Phenolic Compounds ◽  
Enrichment Factors ◽  
Liquid Extraction ◽  
Fast Method ◽  
Effective Parameters ◽  
Homogeneous Liquid ◽  
Liquid Liquid Extraction ◽  
Dispersive Liquid Liquid Microextraction ◽  
Liquid Microextraction

<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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