Monitoring Poly(methyl methacrylate) and Polyvinyl Dichloride Micro/Nanoplastics in Water by Direct Solid-Phase Microextraction Coupled to Gas Chromatography–Mass Spectrometry

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL Analytical Chemistry Pub Date : 2024-06-20 DOI:10.1021/acs.analchem.4c01900
Shengrui Xu*, Huimin Li, Li Xiao, Suling Feng, Jing Fan* and Janusz Pawliszyn, 
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Abstract

A simple, sustainable, and sensitive monitoring approach of micro/nanoplastics (MNPs) in aqueous samples is crucial since it helps in assessing the extent of contamination and understanding the potential risks associated with their presence without causing additional stress to the environment. In this study, a novel strategy for qualitative and quantitative determination of MNPs in water by direct solid-phase microextraction (SPME) coupled with gas chromatography–mass spectrometry (GC-MS) was proposed for the first time. Spherical poly(methyl methacrylate) (PMMA) and irregularly shaped polyvinyl dichloride (PVDC) were used to evaluate the feasibility and performance of the proposed method. The results demonstrated that both PMMA and PVDC MNPs were efficiently extracted by the homemade SPME coating of nitrogen-doped porous carbons (N-SPCs) and exhibited sufficient thermal decomposition in the GC-MS injection port. Excellent extraction performances of N-SPCs coating for MNPs are attributed to hydrophobic cross-linking, electrostatic forcing, hydrogen bonding, and pore trapping. Methyl methacrylate was identified as the marker for PMMA, while 1,3-dichlorobenzene and 1,3,5-trichlorobenzene were the indicators for PVDC. Under the optimal extraction and decomposition conditions, the proposed method exhibited ultrahigh sensitivity, with a limit of detection of 0.0041 μg/L for PMMA and 0.0054 μg/L for PVDC. Notably, a programmed temperature strategy for the GC-MS injector was developed to discriminate and eliminate the potential interferences of intrinsic indicator compounds. Owing to the integration of sampling, extraction, injection, and decomposition into one step by SPME, the proposed method demonstrates exceptional sensitivity, eliminating the necessity for complex sample pretreatment procedures and the use of organic solvents. Finally, the proposed method was successfully applied in the determination of PMMA and PVDC MNPs in real aqueous samples.

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通过直接固相微萃取-气相色谱-质谱联用技术监测水中的聚甲基丙烯酸甲酯和聚氯乙烯微/纳米塑料。
对水样本中的微/纳米塑料(MNPs)进行简单、可持续且灵敏的监测至关重要,因为这有助于评估污染程度并了解其存在的潜在风险,同时不会对环境造成额外压力。本研究首次提出了一种通过直接固相微萃取(SPME)结合气相色谱-质谱法(GC-MS)对水中的 MNPs 进行定性和定量测定的新策略。采用球形聚甲基丙烯酸甲酯(PMMA)和不规则形聚二氯乙烯(PVDC)评估了该方法的可行性和性能。结果表明,自制的掺氮多孔碳(N-SPCs)SPME 涂层能有效地萃取 PMMA 和 PVDC MNPs,并在 GC-MS 进样口表现出充分的热分解。N-SPCs 涂层对 MNPs 的优异萃取性能归功于疏水交联、静电强迫、氢键和孔隙捕集。甲基丙烯酸甲酯被确定为 PMMA 的标记物,而 1,3-dichlorobenzene 和 1,3,5-trichlorobenzene 则是 PVDC 的指示物。在最佳萃取和分解条件下,该方法具有超高灵敏度,PMMA 的检出限为 0.0041 μg/L,PVDC 的检出限为 0.0054 μg/L。值得注意的是,为 GC-MS 进样器开发了一种程序温度策略,以区分和消除内在指示化合物的潜在干扰。由于 SPME 将取样、萃取、进样和分解整合为一个步骤,因此该方法具有极高的灵敏度,无需复杂的样品前处理程序和使用有机溶剂。最后,该方法被成功应用于实际水样中 PMMA 和 PVDC MNPs 的测定。
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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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