2024 : 4 : 27
Mohammad Reza Hadjmohammadi

Mohammad Reza Hadjmohammadi

Academic rank: Professor
ORCID:
Education: PhD.
ScopusId:
Faculty: Faculty of Chemistry
Address: Babolsar
Phone: 01135302350

Research

Title
Application of non-ionic surfactant as a developed method for the enhancement of two-phase solvent bar microextraction for the simultaneous determination of three phthalate esters from water samples
Type
JournalPaper
Keywords
High performance liquid chromatography;Non-ionic surfactant; Phthalate esters; Solvent bar microextraction; Water samples
Year
2018
Journal Journal of Chromatography
DOI
Researchers samereh Ranjbar ، Mohammad Reza Hadjmohammadi

Abstract

The extraction of phthalate esters (PEs) from aqueous matrices using two-phase solvent bar microextraction by organic micellar phase was investigated. A short hollow fiber immobilized with reverse micelles of Brij 35 surfactant in 1-octanol was served as the solvent bar for microextraction. Experimental results show that the extraction efficiency were much higher using two-phase solvent bar microextraction based on non-ionic surfactant than conventional two-phase solvent bar microextraction because of a positive effect of surfactant-containing extraction phase in promoting the partition process by non-ionic intermolecular forces such as polar and hydrophobicity interactions. The nature of the extraction solvent, type and concentration of non-ionic surfactant, extraction time, sample pH, temperature, stirring rate and ionic strength were the effecting parameters which optimized to obtain the highest extraction recovery. Analysis of recovered analytes was carried out with high performance liquid chromatography coupled with ultraviolet detection (HPLC–UV). Under the optimum conditions, linearity was observed in the range of 1–800 ng mL−1 for dimethylphthalate (DMP) and 0.5–800 ng mL−1 for diethylphthalate (DEP) and di-n-butyl phthalate (DBP) with correlation determination values above 0.99 for them. The limits of detection and quantification were ranged from 0.012 to 0.03 ng mL−1 and 0.04–0.1 ng mL−1, respectively. The ranges of intra-day and inter-day RSD (n = 3) at 20 ng mL−1 of PEs were 1.8–2.1% and 2.1–2.6%, respectively. Results showed that developed method can be a very powerful, innovative and promising sample preparation technique in PEs analysis from environmental and drinking water samples.