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基于金属有机框架复合气凝胶的分散固相萃取-超高效液相色谱-串联质谱法测定水中七种苯氧羧酸类除草剂

[Determination of seven phenoxy carboxylic acid herbicides in water using dispersive solid phase extraction coupled with ultra-high performance liquid chromatography-tandem mass spectrometry based on metal-organic framework composite aerogel].

作者信息

Zhang Xin, Wu Ge-Ge, Cui Wen-Lian, Li Shuang, Ma Ji-Ping

机构信息

College of Environmental and Municipal Engineering, Qingdao University of Technology, Qingdao 266000, China.

Qingdao Ecological Environment Monitoring Center of Shandong Province, Qingdao 266000, China.

出版信息

Se Pu. 2024 Nov;42(11):1042-1051. doi: 10.3724/SP.J.1123.2024.01005.

DOI:10.3724/SP.J.1123.2024.01005
PMID:39449511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11519771/
Abstract

Phenoxy carboxylic acid herbicides (PCAs) are difficult to degrade and, thus, pose significant threats to the environment and human health. The limit for 2,4-dichlorophenoxyacetic acid is 30 μg/L in China's standards for drinking water quality, 70 μg/L in the United States' drinking water standards, and 30 μg/L in the World Health Organization's guidelines for drinking water quality. Therefore, the development of an effective detection method for trace PCAs in water is a crucial endeavor. Metal-organic frameworks (MOFs) are novel porous materials that possess advantages such as a large specific surface area, adjustable pore size, and abundant active sites. They exhibit excellent adsorption capability for various compounds. However, the applications of MOFs as adsorbents are limited. For example, the process of isolating powdered MOFs from aqueous solutions is laborious, and microporous MOFs exhibit limited surface affinity, which decreases their mass transfer efficiency in the liquid phase. MOF crystals can be embedded in a substrate to overcome these limitations. Aerogels are obtained by drying hydrogels, which are hydrophilic polymers with a three-dimensional crosslinked network structure. Spongy aerogel materials exhibit unique structural properties such as high porosity, large pore volume, ultralow density, and easy tailorability. When MOFs are combined with an aerogel, their efficient and selective adsorption properties are preserved. In addition, MOF aerogels exhibit a hierarchical porous structure, which enhances the affinity and mass transfer efficiency of the MOF for target molecules. At present, MOF aerogels are primarily prepared by freeze-drying or using supercritical carbon dioxide. These drying processes require significant amounts of energy and time. Hence, the development of greener and more efficient methods to prepare skeleton aerogels is urgently needed. In this study, we prepared an environment-friendly aerogel at ambient temperature and pressure without the use of specialized drying equipment. This ambient-dried MOF composite aerogel was then used for the dispersive solid phase extraction (DSPE) of seven PCAs from environmental water, followed by ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The key parameters affecting the efficiency of DSPE, including the extraction conditions, ratio of MIL-101(Fe)-NH to sodium alginate, pH of the aqueous samples, extraction time, ionic strength (salinity), and elution conditions, such as the elution solvent ratio, elution time, and elution volume, were investigated to obtain optimal extraction efficiency. The adsorbent could adsorb the target contaminants within 12 min, and the analytes could be completely desorbed within 30 s by elution with 4 mL of 1.5% (v/v) formic acid in methanol solution. The water samples could be analyzed without pH adjustment. The main adsorption mechanisms were electrostatic interactions and conjugation. Thus, a new method based on MOF aerogels coupled with UHPLC-MS/MS was developed for the determination of the seven PCA residues in water. The calibration curves for the seven PCAs showed good linearity (≥0.9986), with limits of detection (LODs) and quantification (LOQs) ranging from 0.30 to 1.52 ng/L and from 1.00 to 5.00 ng/L, respectively. Good intra- and inter-day precision values of 6.5%-17.1% and 7.4%-19.4%, respectively, were achieved under low (8 ng/L), medium (80 ng/L), and high (800 ng/L) spiking levels. The developed method was applied to the detection of PCAs in surface water, seawater, and waste leachate, and the detected mass concentrations ranged from 0.6 to 19.3 ng/L. Spiked recovery experiments were conducted at mass concentrations of 8, 80, and 800 ng/L, and the recoveries ranged from 61.7% to 120.3%. The proposed method demonstrates good sensitivity, precision, and accuracy, and has potential applications in the detection of trace PCAs in environmental water.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/523c43edacf6/cjc-42-11-1042-img_6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/7d917ccb833f/cjc-42-11-1042-img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/768df19fa6c4/cjc-42-11-1042-img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/c5e3a66d6cdf/cjc-42-11-1042-img_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/5779c1085c34/cjc-42-11-1042-img_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/a0f66390db48/cjc-42-11-1042-img_5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/523c43edacf6/cjc-42-11-1042-img_6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/7d917ccb833f/cjc-42-11-1042-img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/768df19fa6c4/cjc-42-11-1042-img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/c5e3a66d6cdf/cjc-42-11-1042-img_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/5779c1085c34/cjc-42-11-1042-img_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/a0f66390db48/cjc-42-11-1042-img_5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248c/11519771/523c43edacf6/cjc-42-11-1042-img_6.jpg
摘要

苯氧羧酸类除草剂(PCAs)难以降解,因此对环境和人类健康构成重大威胁。中国饮用水水质标准中2,4-二氯苯氧乙酸的限值为30μg/L,美国饮用水标准中为70μg/L,世界卫生组织饮用水水质准则中为30μg/L。因此,开发一种有效的水中痕量PCAs检测方法是一项至关重要的工作。金属有机框架材料(MOFs)是新型多孔材料,具有比表面积大、孔径可调、活性位点丰富等优点。它们对各种化合物表现出优异的吸附能力。然而,MOFs作为吸附剂的应用受到限制。例如,从水溶液中分离粉末状MOFs的过程很费力,微孔MOFs的表面亲和力有限,这降低了它们在液相中的传质效率。MOF晶体可以嵌入基质中以克服这些限制。气凝胶是通过干燥水凝胶获得的,水凝胶是具有三维交联网络结构的亲水性聚合物。海绵状气凝胶材料具有独特的结构特性,如高孔隙率、大孔体积、超低密度和易于定制。当MOFs与气凝胶结合时,它们高效和选择性的吸附性能得以保留。此外,MOF气凝胶具有分级多孔结构,这提高了MOF对目标分子的亲和力和传质效率。目前,MOF气凝胶主要通过冷冻干燥或使用超临界二氧化碳制备。这些干燥过程需要大量的能量和时间。因此,迫切需要开发更绿色、更高效的方法来制备骨架气凝胶。在本研究中,我们在常温常压下制备了一种环保气凝胶,无需使用专门的干燥设备。然后将这种常温干燥的MOF复合气凝胶用于从环境水中分散固相萃取(DSPE)七种PCAs,随后进行超高效液相色谱-串联质谱(UHPLC-MS/MS)分析。研究了影响DSPE效率的关键参数,包括萃取条件、MIL-101(Fe)-NH与海藻酸钠的比例、水样的pH值、萃取时间、离子强度(盐度)以及洗脱条件,如洗脱溶剂比例、洗脱时间和洗脱体积,以获得最佳萃取效率。吸附剂可在12分钟内吸附目标污染物,通过用4mL 1.5%(v/v)甲酸甲醇溶液洗脱,分析物可在30秒内完全解吸。水样无需调节pH值即可进行分析。主要吸附机制是静电相互作用和共轭作用。因此,开发了一种基于MOF气凝胶与UHPLC-MS/MS联用的新方法来测定水中的七种PCA残留。七种PCAs的校准曲线显示出良好的线性(≥0.9986),检测限(LODs)和定量限(LOQs)分别为0.30至1.52 ng/L和1.00至5.00 ng/L。在低(8 ng/L)、中(80 ng/L)和高(800 ng/L)加标水平下,日内和日间精密度分别为6.(此处原文有误,应为6.5%)-17.1%和7.4%-19.4%。所开发的方法应用于地表水、海水和垃圾渗滤液中PCAs的检测,检测到的质量浓度范围为0.6至19.3 ng/L。在8、80和800 ng/L的质量浓度下进行加标回收实验,回收率范围为61.7%至120.3%。所提出的方法具有良好的灵敏度、精密度和准确度,在环境水中痕量PCAs的检测中具有潜在应用价值。

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