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通过光物理评估抗生素与三嗪多孔有机聚合物吸附剂之间的相互作用。

Assessing interactions between antibiotics and triazine porous organic polymeric sorbents by photophysics.

机构信息

University of Coimbra, CQC-IMS, Department of Chemistry, Rua Larga, 3004-535, Coimbra, Portugal.

University of Coimbra, CQC-IMS, Department of Chemistry, Rua Larga, 3004-535, Coimbra, Portugal.

出版信息

Environ Pollut. 2024 Dec 15;363(Pt 2):125197. doi: 10.1016/j.envpol.2024.125197. Epub 2024 Oct 26.

DOI:10.1016/j.envpol.2024.125197
PMID:39490507
Abstract

This study purposes three triazine-based porous organic polymers (T-POPs 1-3) as advanced platforms for the early detection of antibiotic-polluted environments and effective water decontamination, in order to mitigate water pollution and antimicrobial resistance, which are two huge current problems damaging ecosystems and human health. T-POPs exhibited good performances as adsorbents for the removal of sulfamethazine (SMT) and tetracycline (TC) from water, with efficiencies up to 97% and 96%, and maximum adsorption capacities between (0.36-0.44) and (0.21-0.27) mmol g, respectively, which are similar or even higher (up to 40.3 times) than those reported for other materials. In addition, good reusability was achieved, particularly for T-POP2, despite being the polymer with the lowest surface area. A slightly higher selectivity of T-POPs for sulfonamides and the best performance of T-POP3 to remove six antibiotics from a micromolar solution were observed. T-POPs also acted as fluorescent chemosensors, since T-POP1 underwent linear Stern-Volmer fluorescence quenching in the presence of both SMT and TC, while the enhanced-fluorescent T-POP2 and T-POP3 experienced fluorescence extinction through a sphere of action mechanism in contact with TC, and bathochromic shift accompanied by a hyperchromic effect on the new fluorescent region with the increase in SMT concentration. Thus, T-POP2 and T-POP3 can both promote a selective on-site monitoring of each drug in contaminated water streams and an efficient water remediation, thanks to the synergy between hydrogen and van der Waals interactions. In summary, these triazine-based porous organic polymers are promising materials for the simultaneous monitoring and treatment of antibiotic-containing water and wastewaters.

摘要

本研究旨在开发三种基于三嗪的多孔有机聚合物(T-POPs1-3),作为早期检测抗生素污染环境和有效水净化的先进平台,以减轻水污染和抗生素耐药性问题,这两个问题对生态系统和人类健康造成了巨大的威胁。T-POPs 作为吸附剂,在水中去除磺胺甲恶唑(SMT)和四环素(TC)时表现出良好的性能,去除效率高达 97%和 96%,最大吸附容量分别为(0.36-0.44)和(0.21-0.27)mmol g,与其他材料相比,这些值相似甚至更高(最高可达 40.3 倍)。此外,T-POP2 的可重复使用性非常好,尽管它是比表面积最低的聚合物。T-POPs 对磺胺类药物的选择性略高,T-POP3 从微摩尔溶液中去除六种抗生素的性能最好。T-POPs 还可以作为荧光化学传感器,因为 T-POP1 在存在 SMT 和 TC 的情况下发生线性 Stern-Volmer 荧光猝灭,而增强荧光的 T-POP2 和 T-POP3 通过与 TC 接触的作用机制发生荧光猝灭,并且随着 SMT 浓度的增加,在新的荧光区域发生红移和增色效应。因此,T-POP2 和 T-POP3 都可以促进对受污染水流中每种药物的选择性现场监测和高效水修复,这得益于氢键和范德华相互作用的协同作用。总之,这些基于三嗪的多孔有机聚合物是同时监测和处理含抗生素水和废水的有前途的材料。

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