基于海藻酸钠接枝聚(3-氨基苯酚)/银装饰金属有机框架的抗菌纳米生物吸附剂去除新霉素抗生素

Sara Soltanieh , Ehsan Nazarzadeh Zare , Matineh Ghomi , Fereshte Hassanzadeh Afruzi
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引用次数: 0

摘要

抗生素广泛应用于人类和动物医学,由于其在使用后仍持续存在,因此对水质构成了严重威胁。抗生素在水中的不溶性和对传统去除方法的耐受性加剧了其对环境的影响。本研究旨在通过原位共聚技术开发一种抗菌复合材料--藻酸盐接枝聚(3-氨基苯酚)/银装饰金属有机框架(SA-g-P3AP@MOF(Fe)/Ag)。事实证明,这种复合材料能有效去除污染水中的新霉素。通过傅立叶变换红外光谱(FTIR)、X射线衍射(XRD)、BET和热重分析(TGA)进行的表征证实了该复合材料的结构和性能。在优化条件下(pH=7、30 分钟接触时间、5 毫克吸附剂用量、25 °C 温度和 700 毫克/升污染物浓度),该复合材料从水样中去除了 87% 的新霉素。新霉素与复合材料之间的相互作用符合 Freundlich 等温线,最大吸附容量(Qmax)为 625 毫克/克,并符合假二阶动力学。热力学分析表明,新霉素在合成复合材料上的吸附具有放热和自发性质。所提出的吸附机理集中于 SA-g-P3AP@MOF(Fe)/Ag 的胺、醇和亚胺官能团与新霉素抗生素之间的分子间相互作用。MOF(Fe)/Ag的高孔隙结构大大增强了对新霉素的吸附,从而提高了SA-g-P3AP@MOF(Fe)/Ag的抗菌效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Neomycin antibiotic removal by antimicrobial nanobiosorbent based on sodium alginate-grafted-poly(3-aminophenol)/silver-decorated metal-organic frameworks

Antibiotics, widely used in human and animal medicine, pose a significant threat to water quality due to their persistent presence even after use. Their insolubility in water and resistance to conventional removal methods exacerbate their environmental impact. This study aimed to develop an antimicrobial composite, alginate-grafted-poly(3-aminophenol)/silver-decorated metal-organic framework (SA-g-P3AP@MOF(Fe)/Ag) via an in-situ copolymerization technique. This composite proved effective in removing neomycin from contaminated water. Characterization via FTIR, XRD, BET, and TGA analyses confirmed the composite's structure and properties. Under optimized conditions (pH = 7, 30-minute contact time, 5 mg adsorbent amount, 25 °C temperature, and 700 mg/L pollutant concentration), the composite removed 87 % of neomycin from water samples. The interaction between neomycin and the composite aligned with the Freundlich isotherm, exhibiting a maximum adsorption capacity (Qmax) of 625 mg/g, and adhered to the pseudo-second-order kinetic. Thermodynamic analysis indicated the exothermic and spontaneous nature of neomycin adsorption onto the synthesized composite. The proposed adsorption mechanism centered on intermolecular interactions between amine, alcohol, and imine functional groups of the SA-g-P3AP@MOF(Fe)/Ag and neomycin antibiotic. The incorporation of MOF(Fe)/Ag with its highly porous structure significantly bolstered neomycin adsorption, enhancing the antibacterial effectiveness of SA-g-P3AP@MOF(Fe)/Ag.

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