Fabrication of carboxyl functionalized microporous organic network coated stir bar for efficient extraction and analysis of phenylurea herbicides in food and water samples

• Published in: Journal of Chromatography A Vol. 1640; p. 461947
• Main Authors: Han, Jun-Hua, Cui, Yuan-Yuan, He, Xin-Qiao, Zhang, Yan, Yang, Cheng-Xiong
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15.03.2021
• Subjects: Chromatography, High Pressure Liquid - methods; Food Analysis; Herbicides - analysis; High-performance liquid chromatography; Hydrogen-Ion Concentration; Limit of Detection; Lycopersicon esculentum - chemistry; Malus - chemistry; Microporous organic network; Phenylurea Compounds - analysis; Phenylurea herbicides; Photoelectron Spectroscopy; Porosity; Reproducibility of Results; Spectroscopy, Fourier Transform Infrared; Stir bar sorptive extraction; Thermogravimetry; Time Factors; Water - chemistry; Water Pollutants, Chemical - analysis; Phenylurea herbicides; Stir bar sorptive extraction; High-performance liquid chromatography; Microporous organic network
• ISSN: 0021-9673; 1873-3778
• DOI: 10.1016/j.chroma.2021.461947

Fabrication of novel coatings continues to be an area of great interest and significance in the development and application of stir bar sorptive extraction (SBSE). In this work, a carboxyl-enriched microporous organic network (MON-2COOH) coated stir bar was designed and fabricated as a novel adsorbent for efficient extraction of four phenylurea herbicides (PUHs) before their determination by high-performance liquid chromatography coupled with photodiode array detector (HPLC-PDA). The MON-2COOH was represented as an effective adsorbent for PUHs due to its large surface area, rigid porous structure, aromatic pore walls and the desired hydrogen bonding sites of introduced carboxyl groups. Variables affecting the SBSE of target analytes were optimized in detail. Under the optimal extraction conditions, favorable correlation coefficients (R2 > 0.996) in the linear range 0.10–250 μg L−1, low limits of detection (LODs, S/N = 3) of 0.025–0.070 μg L−1 and good enrichment factors (46–49) were obtained. Besides, the proposed SBSE-HPLC-PDA method was successfully applied to determine trace PUHs in food and environmental water samples with recoveries in the range of 80.0–104.8% and the precisions (relative standard deviations, RSDs) lower than 9.9% (n = 3). This work revealed the potential of MONs in SBSE of trace contaminants from environmental samples.