采用广泛萃取法测定西班牙贝索斯河三角洲河流-地下水界面中的持久性和流动性有机化合物。

IF 8.1 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Chemosphere Pub Date : 2024-11-01 DOI:10.1016/j.chemosphere.2024.143673
Arianna Bautista , Maria Björnsdotter , Carmen Sáez , Anna Jurado , Marta Llorca , Estanislao Pujades , Marinella Farré
{"title":"采用广泛萃取法测定西班牙贝索斯河三角洲河流-地下水界面中的持久性和流动性有机化合物。","authors":"Arianna Bautista ,&nbsp;Maria Björnsdotter ,&nbsp;Carmen Sáez ,&nbsp;Anna Jurado ,&nbsp;Marta Llorca ,&nbsp;Estanislao Pujades ,&nbsp;Marinella Farré","doi":"10.1016/j.chemosphere.2024.143673","DOIUrl":null,"url":null,"abstract":"<div><div>Climate change impacts the Mediterranean region, transforming it from region with a semi-arid climate to a region with an arid climate. Under this situation, while groundwater is an essential hydric resource, its existence is in danger due to anthropogenic pressures. Persistent mobile organic compounds (PMOCs) have recently been recognised as an emerging problem; however, PMOCs in groundwater need to be better characterised. Here, we present a new analytical method to characterise the profile of PMOCs in groundwater based on two parallel solid-phase extraction (SPE), using weak anion exchange and weak cation exchange. Extracts were analysed by ultraperformance liquid chromatography (UPLC) using mix-mode chromatography for those compounds analysed under negative ionisation conditions and hydrophilic interaction liquid chromatography (HILIC) under positive conditions coupled to high-resolution mass-spectrometry (HRMS) using a Q-Exactive Orbitrap™ analyser. For the suspect screening of PMOCs in groundwater, the acquisition mode was in full scan (FS) by “independent scan of all ion fragmentation”. For the tentative identification, different online databases such as Environmental and Food Safety (EFS) HRAM Compound database, PFAS NIST database, ChemSpider for chemical structural information, MzCloud as a mass spectral database, and an in-house list with 1280 PMOC structures have been used. The performance of the method was assessed with 29 representative PMOCs which were selected based on the previous literature. The recovery rates have been between 63 and 110 % for 90 % of the target compounds and method limits of quantification (MLQ) between 0.3 and 10.5 ng/L.</div><div>The optimised approach was applied to assess PMOCs in the Besòs River aquifer, NE Spain, showing 148 tentatively identified structures at confidence levels 1–3. Among them, 66 suspects were tentatively identified at level 3, 54 at level 2, and 28 confirmed at level 1. Most of these compounds were polar and highly polar compounds which are difficult to retain with other extraction approaches. Major detected compounds were pharmaceuticals and personal care products (46), followed by perfluoroalkyl and polyfluoroalkyl substances (PFAS) (32), industrial additives (27), and pesticides (23), among other groups. Some compounds, such as ultrashort chain PFAS and fluorinated betaines, were detected for the first time in groundwaters in Spain.</div></div>","PeriodicalId":276,"journal":{"name":"Chemosphere","volume":"368 ","pages":"Article 143673"},"PeriodicalIF":8.1000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Determination of persistent and mobile organic compounds in the river–groundwater interface of the Besòs river delta, Spain, using a wide extraction approach\",\"authors\":\"Arianna Bautista ,&nbsp;Maria Björnsdotter ,&nbsp;Carmen Sáez ,&nbsp;Anna Jurado ,&nbsp;Marta Llorca ,&nbsp;Estanislao Pujades ,&nbsp;Marinella Farré\",\"doi\":\"10.1016/j.chemosphere.2024.143673\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Climate change impacts the Mediterranean region, transforming it from region with a semi-arid climate to a region with an arid climate. Under this situation, while groundwater is an essential hydric resource, its existence is in danger due to anthropogenic pressures. Persistent mobile organic compounds (PMOCs) have recently been recognised as an emerging problem; however, PMOCs in groundwater need to be better characterised. Here, we present a new analytical method to characterise the profile of PMOCs in groundwater based on two parallel solid-phase extraction (SPE), using weak anion exchange and weak cation exchange. Extracts were analysed by ultraperformance liquid chromatography (UPLC) using mix-mode chromatography for those compounds analysed under negative ionisation conditions and hydrophilic interaction liquid chromatography (HILIC) under positive conditions coupled to high-resolution mass-spectrometry (HRMS) using a Q-Exactive Orbitrap™ analyser. For the suspect screening of PMOCs in groundwater, the acquisition mode was in full scan (FS) by “independent scan of all ion fragmentation”. For the tentative identification, different online databases such as Environmental and Food Safety (EFS) HRAM Compound database, PFAS NIST database, ChemSpider for chemical structural information, MzCloud as a mass spectral database, and an in-house list with 1280 PMOC structures have been used. The performance of the method was assessed with 29 representative PMOCs which were selected based on the previous literature. The recovery rates have been between 63 and 110 % for 90 % of the target compounds and method limits of quantification (MLQ) between 0.3 and 10.5 ng/L.</div><div>The optimised approach was applied to assess PMOCs in the Besòs River aquifer, NE Spain, showing 148 tentatively identified structures at confidence levels 1–3. Among them, 66 suspects were tentatively identified at level 3, 54 at level 2, and 28 confirmed at level 1. Most of these compounds were polar and highly polar compounds which are difficult to retain with other extraction approaches. Major detected compounds were pharmaceuticals and personal care products (46), followed by perfluoroalkyl and polyfluoroalkyl substances (PFAS) (32), industrial additives (27), and pesticides (23), among other groups. Some compounds, such as ultrashort chain PFAS and fluorinated betaines, were detected for the first time in groundwaters in Spain.</div></div>\",\"PeriodicalId\":276,\"journal\":{\"name\":\"Chemosphere\",\"volume\":\"368 \",\"pages\":\"Article 143673\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2024-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemosphere\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0045653524025736\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemosphere","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0045653524025736","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

气候变化影响着地中海地区,使其从半干旱气候地区转变为干旱气候地区。在这种情况下,虽然地下水是一种重要的水文资源,但由于人为压力,地下水的存在岌岌可危。持久性移动有机化合物(PMOCs)最近已被认为是一个新出现的问题;然而,地下水中的 PMOCs 还需要更好地定性。在此,我们提出了一种新的分析方法,利用弱阴离子交换和弱阳离子交换两种平行的固相萃取(SPE)来描述地下水中 PMOCs 的特征。萃取物采用超高效液相色谱法(UPLC)进行分析,在负离子条件下采用混合模式色谱法分析化合物,在正离子条件下采用亲水作用液相色谱法(HILIC),并使用 Q-Exactive Orbitrap™ 分析仪进行高分辨率质谱分析(HRMS)。在对地下水中的 PMOCs 进行可疑筛选时,采用了 "所有离子碎片独立扫描 "的全扫描(FS)采集模式。为了进行初步鉴定,使用了不同的在线数据库,如环境与食品安全(EFS)HRAM 化合物数据库、PFAS NIST 数据库、化学结构信息 ChemSpider、作为质谱数据库的 MzCloud 以及包含 1280 种 PMOC 结构的内部列表。根据以前的文献资料,选择了 29 种有代表性的 PMOC 对该方法的性能进行了评估。90% 目标化合物的回收率在 63-110% 之间,方法定量限 (MLQ) 在 0.3-10.5 纳克/升之间。该优化方法被用于评估西班牙东北部贝索斯河含水层中的 PMOCs,结果显示,在置信度为 1-3 级的情况下,有 148 个结构被初步确定。其中,66 个疑似结构被初步确定为第 3 级,54 个被确定为第 2 级,28 个被确定为第 1 级。这些化合物大多是极性和高极性化合物,其他萃取方法难以保留。检测到的主要化合物是药品和个人护理产品(46 种),其次是全氟烷基和多氟烷基物质(PFAS)(32 种)、工业添加剂(27 种)和杀虫剂(23 种)等。西班牙首次在地下水中检测到超短链 PFAS 和含氟甜菜碱等化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Determination of persistent and mobile organic compounds in the river–groundwater interface of the Besòs river delta, Spain, using a wide extraction approach
Climate change impacts the Mediterranean region, transforming it from region with a semi-arid climate to a region with an arid climate. Under this situation, while groundwater is an essential hydric resource, its existence is in danger due to anthropogenic pressures. Persistent mobile organic compounds (PMOCs) have recently been recognised as an emerging problem; however, PMOCs in groundwater need to be better characterised. Here, we present a new analytical method to characterise the profile of PMOCs in groundwater based on two parallel solid-phase extraction (SPE), using weak anion exchange and weak cation exchange. Extracts were analysed by ultraperformance liquid chromatography (UPLC) using mix-mode chromatography for those compounds analysed under negative ionisation conditions and hydrophilic interaction liquid chromatography (HILIC) under positive conditions coupled to high-resolution mass-spectrometry (HRMS) using a Q-Exactive Orbitrap™ analyser. For the suspect screening of PMOCs in groundwater, the acquisition mode was in full scan (FS) by “independent scan of all ion fragmentation”. For the tentative identification, different online databases such as Environmental and Food Safety (EFS) HRAM Compound database, PFAS NIST database, ChemSpider for chemical structural information, MzCloud as a mass spectral database, and an in-house list with 1280 PMOC structures have been used. The performance of the method was assessed with 29 representative PMOCs which were selected based on the previous literature. The recovery rates have been between 63 and 110 % for 90 % of the target compounds and method limits of quantification (MLQ) between 0.3 and 10.5 ng/L.
The optimised approach was applied to assess PMOCs in the Besòs River aquifer, NE Spain, showing 148 tentatively identified structures at confidence levels 1–3. Among them, 66 suspects were tentatively identified at level 3, 54 at level 2, and 28 confirmed at level 1. Most of these compounds were polar and highly polar compounds which are difficult to retain with other extraction approaches. Major detected compounds were pharmaceuticals and personal care products (46), followed by perfluoroalkyl and polyfluoroalkyl substances (PFAS) (32), industrial additives (27), and pesticides (23), among other groups. Some compounds, such as ultrashort chain PFAS and fluorinated betaines, were detected for the first time in groundwaters in Spain.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Chemosphere
Chemosphere 环境科学-环境科学
CiteScore
15.80
自引率
8.00%
发文量
4975
审稿时长
3.4 months
期刊介绍: Chemosphere, being an international multidisciplinary journal, is dedicated to publishing original communications and review articles on chemicals in the environment. The scope covers a wide range of topics, including the identification, quantification, behavior, fate, toxicology, treatment, and remediation of chemicals in the bio-, hydro-, litho-, and atmosphere, ensuring the broad dissemination of research in this field.
期刊最新文献
Integration of Fe-MOF-laccase-magnetic biochar: From Rational Designing of a biocatalyst to aflatoxin B1 decontamination of peanut oil Evaluation of extraction and storage conditions for quantification and characterization of silver nanoparticles in complex samples by single particle-ICP-MS Neurotoxicology of warfare arsenical, diphenylarsinic acid in humans and experimental models Role of molybdenum compounds in enhancing denitrification: Structure-activity relationship and the regulatory mechanisms Percutaneous absorption of two bisphenol a analogues, BPAF and TGSA: Novel In vitro data from human skin
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1