A heteropore covalent organic framework for highly selective enrichment of aryl-organophosphate esters in environmental water coupled with UHPLC-MS/MS determination

被引:9
作者
Cheng, Jiawen [1 ]
Ma, Jiping [1 ]
Li, Shuang [1 ]
Wang, Shasha [1 ]
Huang, Chaonan [1 ]
Lv, Min [2 ]
Li, Jinhua [2 ]
Wang, Xiaoyan [4 ]
Chen, Lingxin [2 ,3 ]
机构
[1] Qingdao Univ Technol, Sch Environm & Municipal Engn, Qingdao 266033, Peoples R China
[2] Chinese Acad Sci, Yantai Inst Coastal Zone Res, CAS Key Lab Coastal Environm Proc & Ecol Remediat, Shandong Key Lab Coastal Environm Proc, Yantai 264003, Peoples R China
[3] Pilot Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao 266237, Peoples R China
[4] Binzhou Med Univ, Sch Pharm, Yantai 264003, Peoples R China
基金
中国国家自然科学基金;
关键词
Aryl-organophosphate esters; Heteropore covalent organic framework; Melamine sponge; Vortex-assisted extraction; Environmental water; SOLID-PHASE MICROEXTRACTION; PI-PI INTERACTION; FLAME RETARDANTS; CRYSTALLINE; FIBER;
D O I
10.1016/j.jhazmat.2023.132613
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The identification of an increasing number of aryl organophosphate esters (aryl-OPEs) in environmental samples has led to growing attention recently. Due to the potential adverse effects on human health and environment, development of new analytical methods for sensitive and selective determination of aryl-OPEs in complex matrices is urgently needed. Here, a novel analytical method for the identification and determination of trace amounts of aryl-OPEs in water samples is developed by using melamine sponge@heteropore covalent organic framework (MS@HCOF) based on vortex-assisted extraction (VAE) prior to UHPLC-MS/MS analysis. The MS@HCOF was rationally designed and synthesized through an in-situ growth strategy and exhibited superior selectivity toward aryl-OPEs compared with that of MS@singlepore COF (MS@SCOF) due to steric effect. A systematic optimization was conducted on important parameters of VAE, resulting in the successful extraction of nine aryl-OPEs in just 6 min. Under optimized conditions, the limits of detection (S/N = 3) and quantification (S/ N = 10) were within the ranges of 0.001-0.027 and 0.005-0.091 ng/L for nine aryl-OPEs, respectively. The validated method was proven applicable to real water samples, i.e., the recoveries were 65.3-119.5 % for seawater, 59.4-112.9 % for effluent, and 76.0-117.4 % for tap water. Furthermore, the adsorption mechanisms were explored through density functional theory (DFT) calculations. DFT results revealed that a notable selective enrichment capacity of MS@HCOF towards aryl-OPEs stems from 7C-7C conjugation and hydrogen bonding. The established method benefits from the advantages of high selectivity and sensitivity for the ultra-trace determi-nation of aryl-OPEs.
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页数:11
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