Waste PET Plastic-Derived UIO-66(Zr)-MOF Adsorbent for Dispersive Solid Phase Extraction and Removal of Penicillin Antibiotics Water Systems

用于分散固相萃取和去除水系统中青霉素类抗生素的废弃PET塑料衍生UIO-66(Zr)-MOF吸附剂

阅读:1

Abstract

The extensive use or misuse of broad-spectrum antibiotics such as penicillins and their existence in various water bodies is still one of increasing global concern due to their persistent nature, which could potentially lead to human health and environmental risks. Recycling or upcycling plastic waste to value-added products such as metal-organic frameworks (MOF) to solve other environmental problems, such as water pollution, has received more attention. As a result, UiO-66(Zr)-MOF derived from recycled waste PET bottles (PET-derived UiO-66(Zr)-MOF) was investigated for enrichment and removal of amoxicillin (AMX) and penicillin G (PNG) in water bodies. The synthesised adsorbent was characterised using different analytical characterisation techniques. UiO-66(Zr)-MOF produced the maximum adsorption capacities of 139 and 147 mg/g for AMX and PNG, respectively. Freundlich and pseudo-second-order kinetics models best explained the adsorption process. The dispersive micro-solid phase extraction (D-μ-SPE) of the target analytes was performed using a high-performance liquid chromatography-diode array detector (HPLC-DAD). The effectiveness of the developed method was confirmed by its remarkable analytical performances, such as limits of detection (0.19-0.21 µg/L) while the linear range was 0.6-1000 µg/L. The feasibility and applicability of the validated UiO-66(Zr)-MOF-D-μ-SPE/HPLC-DAD method were confirmed by applying it in real water analysis. The AMX and PNG were detected in wastewater samples in the ranges of 1.51-4.71 µg/L and 0.195-1.19 µg/L for influent and effluent. The spike recoveries ranged from 89.9% to 101%, while the precision (intraday and interday) of the method was less than 5%.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。