{"title":"利用正交液相色谱分离模式,对巴塞罗那城市地下水中的极性和高极性有机污染物进行液相色谱-质谱联用分析。","authors":"Francesc Labad, Sandra Pérez","doi":"10.1007/s11356-024-33471-y","DOIUrl":null,"url":null,"abstract":"<div><p>Groundwater samples may contain thousands of organic pollutants from infiltration of surface water, sewer leakages, and to a minor extent from public water supply network losses. Polar (0 < log <i>D</i> < − 2.0) and very polar substances (log <i>D</i> < − 2.0) have been largely beyond the scope of applied analytical methodologies in environmental monitoring because of challenges related to their extraction from the sample and subsequent chromatographic separation. In this study, we developed an analytical workflow for 96 pollutants covering a broad polarity range, including pharmaceuticals, industrial chemicals, and artificial sweeteners, potentially seeping through the soil in urban areas. The Besos aquifer located at the Northern-eastern edge of the city of Barcelona was chosen as a study area due to the deterioration of the quality of the aquifers over the past years and the proven presence of numerous pollutants. The methodology consisted of vacuum-assisted evaporation (VAE) followed by chromatographic separation of the sample on two columns with orthogonal retention mechanisms, namely, an HSS T3 column (modified C18) and a BEH amide column (HILIC). The analytes were detected by high-resolution mass spectrometry on a Q Exactive Orbitrap system in data-independent acquisition mode. Taking into consideration the retention as well as the peak shape, a Quality Score (QS) was assigned for each analyte to evaluate the quality of each chromatographic peak of each compound. While 67 compounds, including 19 polar and 48 moderately polar, were satisfactorily retained on an HSS T3, 29 compounds, including 14 highly polar, 14 polar, and one moderately polar, were analyzed in the BEH amide column. The optimized methodology was applied for the analysis of 89 out of 96 validated contaminants with satisfactory recoveries in samples collected from seven wells, providing low LODs (0.02 to 0.45 ng L<sup>−1</sup>) and LOQs (0.06 to 1.34 ng L<sup>−1</sup>). A number of highly polar and polar compounds not previously reported to occur in GW, including artificial sweeteners, pharmaceuticals, and industrial chemicals, were detected at concentrations as high as few <span>\\(\\mu\\)</span>g L<sup>−1</sup>.</p></div>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":"33 22","pages":"11018 - 11028"},"PeriodicalIF":5.8000,"publicationDate":"2024-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s11356-024-33471-y.pdf","citationCount":"0","resultStr":"{\"title\":\"LC–MS analysis of polar and highly polar organic pollutants in Barcelona urban groundwater using orthogonal LC separation modes\",\"authors\":\"Francesc Labad, Sandra Pérez\",\"doi\":\"10.1007/s11356-024-33471-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Groundwater samples may contain thousands of organic pollutants from infiltration of surface water, sewer leakages, and to a minor extent from public water supply network losses. Polar (0 < log <i>D</i> < − 2.0) and very polar substances (log <i>D</i> < − 2.0) have been largely beyond the scope of applied analytical methodologies in environmental monitoring because of challenges related to their extraction from the sample and subsequent chromatographic separation. In this study, we developed an analytical workflow for 96 pollutants covering a broad polarity range, including pharmaceuticals, industrial chemicals, and artificial sweeteners, potentially seeping through the soil in urban areas. The Besos aquifer located at the Northern-eastern edge of the city of Barcelona was chosen as a study area due to the deterioration of the quality of the aquifers over the past years and the proven presence of numerous pollutants. The methodology consisted of vacuum-assisted evaporation (VAE) followed by chromatographic separation of the sample on two columns with orthogonal retention mechanisms, namely, an HSS T3 column (modified C18) and a BEH amide column (HILIC). The analytes were detected by high-resolution mass spectrometry on a Q Exactive Orbitrap system in data-independent acquisition mode. Taking into consideration the retention as well as the peak shape, a Quality Score (QS) was assigned for each analyte to evaluate the quality of each chromatographic peak of each compound. While 67 compounds, including 19 polar and 48 moderately polar, were satisfactorily retained on an HSS T3, 29 compounds, including 14 highly polar, 14 polar, and one moderately polar, were analyzed in the BEH amide column. The optimized methodology was applied for the analysis of 89 out of 96 validated contaminants with satisfactory recoveries in samples collected from seven wells, providing low LODs (0.02 to 0.45 ng L<sup>−1</sup>) and LOQs (0.06 to 1.34 ng L<sup>−1</sup>). A number of highly polar and polar compounds not previously reported to occur in GW, including artificial sweeteners, pharmaceuticals, and industrial chemicals, were detected at concentrations as high as few <span>\\\\(\\\\mu\\\\)</span>g L<sup>−1</sup>.</p></div>\",\"PeriodicalId\":545,\"journal\":{\"name\":\"Environmental Science and Pollution Research\",\"volume\":\"33 22\",\"pages\":\"11018 - 11028\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2024-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s11356-024-33471-y.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental Science and Pollution Research\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11356-024-33471-y\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"0\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science and Pollution Research","FirstCategoryId":"93","ListUrlMain":"https://link.springer.com/article/10.1007/s11356-024-33471-y","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
地下水样本可能含有数千种来自地表水渗透、下水道泄漏以及少量来自公共供水网络损失的有机污染物。极性物质(0 &lt; log D &lt;−2.0)和极极性物质(log D &lt;−2.0)在很大程度上已经超出了环境监测中应用分析方法的范围,因为它们从样品中提取和随后的色谱分离存在挑战。在这项研究中,我们开发了96种污染物的分析工作流程,涵盖了广泛的极性范围,包括药物、工业化学品和人工甜味剂,这些污染物可能会渗透到城市地区的土壤中。位于巴塞罗那市东北边缘的贝索斯含水层被选为研究区域,因为过去几年含水层质量的恶化和大量污染物的存在。方法采用真空辅助蒸发法(VAE),然后在HSS T3柱(改良C18)和BEH酰胺柱(HILIC)两种正交保留机制上对样品进行色谱分离。分析物在Q Exactive Orbitrap系统上以数据独立采集模式进行高分辨率质谱检测。考虑到保留和峰形,为每个分析物分配一个质量分数(QS)来评价每个化合物的每个色谱峰的质量。67个化合物,包括19个极性和48个中极性,在HSS T3上被满意地保留,29个化合物,包括14个高极性,14个极性和1个中极性,在BEH酰胺柱上被分析。优化后的方法可用于分析从7口井采集的96种验证污染物中的89种,回收率令人满意,lod (0.02 ~ 0.45 ng L−1)和loq (0.06 ~ 1.34 ng L−1)均较低。许多高极性和极性化合物,包括人工甜味剂、药物和工业化学品,以前没有报道过在GW中出现,在浓度高达\(\mu\) g L−1的情况下被检测到。
LC–MS analysis of polar and highly polar organic pollutants in Barcelona urban groundwater using orthogonal LC separation modes
Groundwater samples may contain thousands of organic pollutants from infiltration of surface water, sewer leakages, and to a minor extent from public water supply network losses. Polar (0 < log D < − 2.0) and very polar substances (log D < − 2.0) have been largely beyond the scope of applied analytical methodologies in environmental monitoring because of challenges related to their extraction from the sample and subsequent chromatographic separation. In this study, we developed an analytical workflow for 96 pollutants covering a broad polarity range, including pharmaceuticals, industrial chemicals, and artificial sweeteners, potentially seeping through the soil in urban areas. The Besos aquifer located at the Northern-eastern edge of the city of Barcelona was chosen as a study area due to the deterioration of the quality of the aquifers over the past years and the proven presence of numerous pollutants. The methodology consisted of vacuum-assisted evaporation (VAE) followed by chromatographic separation of the sample on two columns with orthogonal retention mechanisms, namely, an HSS T3 column (modified C18) and a BEH amide column (HILIC). The analytes were detected by high-resolution mass spectrometry on a Q Exactive Orbitrap system in data-independent acquisition mode. Taking into consideration the retention as well as the peak shape, a Quality Score (QS) was assigned for each analyte to evaluate the quality of each chromatographic peak of each compound. While 67 compounds, including 19 polar and 48 moderately polar, were satisfactorily retained on an HSS T3, 29 compounds, including 14 highly polar, 14 polar, and one moderately polar, were analyzed in the BEH amide column. The optimized methodology was applied for the analysis of 89 out of 96 validated contaminants with satisfactory recoveries in samples collected from seven wells, providing low LODs (0.02 to 0.45 ng L−1) and LOQs (0.06 to 1.34 ng L−1). A number of highly polar and polar compounds not previously reported to occur in GW, including artificial sweeteners, pharmaceuticals, and industrial chemicals, were detected at concentrations as high as few \(\mu\)g L−1.
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