4.6 Article

Preparation of amine-modified amphiphilic resins for the extraction of trace pharmaceuticals and personal care products in environmental waters

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JOURNAL OF CHROMATOGRAPHY A
卷 1701, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.chroma.2023.464062

关键词

Amine-modified; Solid-phase extraction; Amphiphilic resins; Pharmaceuticals and personal care products; SPE; LC-MS; MS

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Four amine-modified amphiphilic resins were synthesized and used as solid-phase extraction materials for enriching pharmaceuticals and personal care products (PPCPs) from water. The materials showed large specific surface area, high ion exchange capacity, and good hydrophilicity. A solid-phase extraction method coupled with ultra-performance liquid chromatography and tandem mass spectrometry was developed, which exhibited good accuracy and sensitivity in determining PPCPs in water samples. This method has great potential for commercial application in trace PPCP extraction from environmental water samples.
Herein, four amine-modified amphiphilic resins were synthesized and utilized as solid-phase extraction (SPE) materials to enrich pharmaceuticals and personal care products (PPCPs) from environmental wa-ter. The obtained materials (Strong anion-exchange amphiphilic materials, SAAMs; Weak anion-exchange amphiphilic materials, WAAMs) possessed large specific surface area (473-626 m2/g), high ion exchange capacity (0.89-1.97 mmol/g), and small contact angle (74.41-79.74 degrees), indicating good hydrophilicity. The main factors affecting the efficiency of the extraction process were studied, including column volume, column flow rate, sample salinity and sample pH. Notably, the trend observed in absolute recovery was significantly correlated with the Zeta potential of the employed adsorbents. Furthermore, based on the obtained materials, a method of SPE coupled with ultra-performance liquid chromatography and tandem mass spectrometry (SPE/LC-MS/MS) was developed, and then utilized to determine PPCPs in the samples collected from the Yangtze River Delta. The Method detection limit (MDL) and Method quantification limit (MQL) ranged from 0.05 to 0.60 ng/L and 0.17 to 2.00 ng/L, respectively, with a relative standard devi-ation (RSD) below 6.3%, demonstrating good accuracy and sensitivity. As evidenced by comparison with previous literature, the developed method exhibited satisfactory performance, showing great potential for further commercial application in the extraction of trace PPCPs from environmental water samples.(c) 2023 Elsevier B.V. All rights reserved.

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