[磁固相萃取-液相色谱-质谱法测定环境水样中的全氟化合物及相关风险评估]。

Chen-Shu Gu, Zhen-Zhen Liu, Hui-Ling Jin, Xiao-Qi Liu, Mei-Yu Wang, Wei-Jie Sun, Yang-Ying Sun, Pei-Pei Qi
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引用次数: 0

摘要

全氟化合物(pfc)被广泛使用,具有持久性,它们在水中的存在引起了重大关注。全氟化合物,特别是短链变体,在水中具有高度可溶性和流动性,这使得它们能够通过河流系统进行长距离运输,可能导致广泛的污染。这些化合物具有抗降解性,这对传统的水处理方法来说是一个挑战,因为传统的水处理方法通常不能有效地去除PFCs,导致它们在水体中长期存在。以磁性聚苯乙烯吡咯烷酮(Fe3O4-PLS)为磁性吸附剂,建立了富集水中11种全氟化合物的磁固相萃取方法。采用纯化的亲脂性PLS磁珠作为固相萃取剂,采用苯基和吡咯烷酮基团对其表面进行改性,以促进含有亲水性官能团和疏水性烷基侧链的全氟碳化合物的吸附。采用液相色谱-串联质谱法(LC-MS/MS)准确、灵敏地测定了水中PFCs的含量。该方法包括将50 mg(±0.05 mg) Fe3O4-PLS精确称重到500 mL烧杯中,加入2 mL甲醇(用于活化),将烧杯放在磁铁上30秒,一旦甲醇和Fe3O4-PLS完全分离,就丢弃甲醇。在烧杯中加入200毫升的混合PFC水溶液,超声15分钟,然后放置在强磁铁上,直到Fe3O4-PLS在烧杯底部完全分离。上层液体被丢弃。加入4 ml含0.1%甲酸的乙腈作为Fe3O4-PLS洗脱液,超声检测30s后,将烧杯置于磁铁上,收集洗脱液。样品在氮气流下干燥,残留物在0.5 mL乙腈中再溶解,超声处理10 s,然后膜过滤,LC-MS/MS分析。11种PFCs在1 ~ 100 μg/L范围内呈良好的线性关系,相关系数(R2)在0.997 ~ 0.999 9范围内。检测限和定量限(lod和loq)分别为0.001 ~ 0.620 ng/L和0.002 ~ 2.065 ng/L,灵敏度较高。在不同浓度(0.05、1、10、50 μg/L)下,11种pfc的回收率为60.8% ~ 120.0%。相对标准偏差(rsd)范围为1.0% ~ 20.0%,满足水体中PFC分析的要求。采用该方法对杭州东苕溪流域15个地点(工厂、水库和居民区附近)11种PFCs的浓度进行了分析。共检测到6种全氟化合物,即全氟辛酸(PFOA)、全氟壬酸(PFNA)、全氟辛烷磺酸(PFOS)、全氟庚酸(PFHpS)、全氟丁烷磺酸(PFBS)和全氟癸酸(PFDA),质量浓度为11.4 ~ 30.7 ng/L。PFOA的最高质量浓度为25.5 ng/L。东苕溪河的全氟化合物主要与前驱体降解和工业废水排放有关。在检测浓度最低的采样点附近,污染水平突然上升,这可能是由于河流码头附近的水力输送过程与湍流较大的流水存在较大的水动力差异。这种差异导致地表水中的悬浮颗粒与再悬浮的沉积物颗粒混合,从而使全氟化合物释放回地表水中。污染水平在延伸的河流及其河口和支流方向上持续下降。风险评估结果显示,东苕溪流域地表水中PFC含量远低于官方健康参考值,尚未达到可能造成生态危害和危害人体健康的水平。这些数据有望通过深入了解发生特征来支持监测系统的改进,并有助于制定东苕溪pfc的管理计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Determination of perfluorinated compounds in environmental water samples by magnetic solid-phase extraction-liquid chromatography-mass spectrometry and associated risk assessment].

[Determination of perfluorinated compounds in environmental water samples by magnetic solid-phase extraction-liquid chromatography-mass spectrometry and associated risk assessment].

[Determination of perfluorinated compounds in environmental water samples by magnetic solid-phase extraction-liquid chromatography-mass spectrometry and associated risk assessment].

[Determination of perfluorinated compounds in environmental water samples by magnetic solid-phase extraction-liquid chromatography-mass spectrometry and associated risk assessment].

Perfluorinated compounds (PFCs) are widely used, persistent, and their presence in water is of significant concern. PFCs, particularly short-chain variants, are highly soluble and mobile in water, which enables their transport over long distances via river systems, potentially leading to extensive contamination. These compounds are resistant to degradation, which is challenging for conventional water-treatment methods that often remove PFCs ineffectively, leading to their prolonged presence in water bodies. This paper establishes a magnetic solid-phase extraction method for 11 PFCs in enriched water using magnetic polystyrene pyrrolidone (Fe3O4-PLS) as a magnetic adsorbent. Purified lipophilic PLS magnetic beads were used as the solid-phase extractant, and their surfaces were modified using phenyl and pyrrolidone groups to facilitate the adsorption of PFCs that contain hydrophilic functional groups and hydrophobic alkyl side chains. PFCs in water were determined accurately and sensitively by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The method involved accurately weighing 50 mg (±0.05 mg) of the Fe3O4-PLS into a 500-mL beaker, adding 2 mL of methanol (for activation), placing the beaker on a magnet for 30 s, and discarding the methanol once the methanol and Fe3O4-PLS had been completely separated. A 200-mL aliquot of an aqueous mixed PFC solution was added to the beaker, sonicated for 15 min, and then placed on a strong magnet until the Fe3O4-PLS had completely separated at the bottom of the beaker. The upper liquid was discarded. A 4-mL acetonitrile containing 0.1% formic acid was added as the Fe3O4-PLS eluent, ultrasonicated for 30 s, after which the beaker was placed on the magnet and the eluate collected. The sample was taken to dryness under a stream of nitrogen, the residue was redissolved in 0.5 mL of acetonitrile, ultrasonicated for 10 s, and then membrane-filtered prior to analysis by LC-MS/MS. The 11 PFCs exhibited good linear relationships ranging from 1 to100 μg/L, with correlation coefficients (R2) ranging from 0.997 6 to 0.999 9. Limits of detection and quantification (LODs and LOQs, respectively) were determined to be 0.001-0.620 ng/L and 0.002-2.065 ng/L, respectively, indicative of high sensitivity. The 11 PFCs exhibited recoveries of 60.8%-120.0% at various concentrations (0.05, 1, 10, and 50 μg/L). Relative standard deviations (RSDs) ranged from 1.0% to 20.0%, which meet the requirements for PFC analysis in water. The concentrations of the 11 PFCs at 15 sites in the Dongtiaoxi River, Hangzhou (near factories, reservoirs and residential areas) were analyzed using the developed method. A total of six PFCs, namely perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorooctane sulfonic acid (PFOS), perfluoroheptanoic acid (PFHpS), perfluorobutanesulfonate (PFBS) and perfluorodecanoic acid (PFDA), were detected at mass concentrations of 11.4-30.7 ng/L. The highest mass concentration of PFOA was determined to be 25.5 ng/L. The PFCs in the Dongtiaoxi River were found to be mainly associated with precursor degradation and industrial wastewater discharge. A sudden rise in the pollution level was observed near the sampling point with the lowest detected concentration, which is possibly ascribable to the strong hydrodynamic difference between the hydraulic transport process near the river wharf and the highly turbulent flowing water. This difference results in the suspended particles in surface water mixing with re-suspended sediment particles such that PFCs are released back into the surface water. Pollution levels were observed to continuously decrease in the directions of the extended river and its estuary and tributaries. Risk assessments revealed that the PFC levels in the surface water of the Dongtiaoxi River basin are much lower than the official health reference value and have not reached levels that are expected to cause ecological harm and risk human health. The data are expected to support monitoring-system improvements by providing an in-depth understanding of occurrence characteristics, and help formulate a management plan for PFCs in the Dongtiaoxi River.

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