2024 : 4 : 30
Milad Ghani

Milad Ghani

Academic rank: Associate Professor
ORCID:
Education: PhD.
ScopusId:
Faculty: Faculty of Chemistry
Address: University of Mazandaran
Phone: 011-35302363

Research

Title
Synthesis of cellulose nanofibers-based ImSalophen@Fe3O4 as a green sorbent for magnetic solid-phase extraction of chlorophenols followed by quantification via high-performance liquid chromatography-ultraviolet detection
Type
JournalPaper
Keywords
Keywords: Salophen Schiff Bases CNF-ImSalophen @Fe3O4 Chlorophenols HPLC-UV Magnetic cellulose nanofiber Honey Bovine milk Black tea Cost-Benefit Analysis
Year
2023
Journal MICROCHEMICAL JOURNAL
DOI
Researchers Milad Ghani ، Sepideh Khodkavandi ، Zahra Jafari ، Pouya Ghamari Kargar ، Behrooz Maleki ، Hadis Fath nia tabari

Abstract

An effective, sensitive, relatively-fast and cost-effective method was developed to determine four types of selected chlorophenols (CPs) including 4-cholorophenol, 2,4-dicholorophenol, 2,5-dicholorophenol and 2,4,6-tricholorophenol in several kinds of honey, black tea and bovine milk samples through applying Cellulose Nano- Fiber (CNF)-ImSalophen@Fe3O4. CNF-ImSalophen@Fe3O4 has been synthesized using a very simple, easy, cost-effective, efficient and fast method. First, a magnetic CNF was used as the substrate. Next, imidazole was created on the surface of the magnetic CNF. Thereafter, the Cl-Salophen Schiff base was accommodated on the prepared magnetic CNF-Im. The prepared sorbent was used for the extraction of selected analytes. The extracted analytes were desorbed via organic solvent and analyzed through high-performance liquid chromatographyultraviolet detection (HPLC-UV). The strong interactions between the sorbent and the selected analytes (intermolecular hydrogen bonding, and π-π interactions) made this sorbent capable of high extraction performance and capacity. Under the optimized condition, the method linearity was in the range of 0.2–500 μg/L for the selected analytes in water. The calibration curves showed a determination of coefficient higher than 0.9986. The limits of detection and limits of quantification were calculated to be between 0.05–0.14 μg/L and 0.16–0.46 μg/L, respectively. In order to calculate the method precision, the inter-day and intra-day relative standard deviations were determined to be between 3.2 and 4.7 % in three selected concentrations. Furthermore, the enrichment factors were found to be 36, 31, 33 and 37 for 4-cholorophenol, 2,4-dicholorophenol, 2,5-dicholorophenol and 2,4,6-tricholorophenol, respectively. Moreover, the calculated absolute recoveries were between 62 and 74 %. The proposed method was also employed for the analysis of various real samples such as honey, bovine milk and black tea. The obtained recoveries indicate