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Preparation of GO/Ni/Y‐MOFs via Microwave‐Assisted Ball Milling and the Removal of Tetracycline Hydrochloride From Aqueous Solutions

化学 水溶液 球磨机 盐酸四环素 核化学 微波食品加热 四环素 盐酸盐 无机化学 化学工程 有机化学 生物化学 量子力学 物理 工程类 抗生素
作者
Fuhua Wei,Min Li,Qinhui Ren,Qin Zhang,Wei Shang,Diaodiao Zhang,Lanyan Tian,Fuhua Wei
出处
期刊:Applied Organometallic Chemistry [Wiley]
卷期号:39 (5) 被引量:3
标识
DOI:10.1002/aoc.70136
摘要

ABSTRACT In this research, GO/Ni/Y‐MOFs were successfully prepared using a microwave‐assisted ball milling (MABM) technique. 1,3,5‐Benzenetricarboxylic acid was utilized as the organic linker, while nickel(II) acetate tetrahydrate and yttrium(III) acetate hydrate acted as the metal sources. The structural and morphological properties of the synthesized materials were examined using Fourier‐transform infrared spectroscopy (FT‐IR), scanning electron microscopy (SEM), X‐ray diffraction (XRD), and nitrogen adsorption–desorption measurements. These materials were subsequently employed to evaluate their efficiency in removing tetracycline hydrochloride from solution. Experimental findings revealed that adding 200 mg of GO/Ni/Y‐MOFs to a solution with an initial concentration of 50 mg/L tetracycline hydrochloride resulted in a remarkable removal efficiency of 87.3% within 2 h. To better understand the kinetic behavior of this process, both pseudo‐first‐order and pseudo‐second‐order kinetic models were investigated. It was observed that the experimental data correlated more closely with the pseudo‐second‐order model predictions. Furthermore, Langmuir, and Freundlich isotherm models were applied to analyze the adsorption characteristics under isothermal conditions. Notably, the experimental results showed a better fit with the Freundlich isotherm compared with the Langmuir isotherm. Based on these experiments, it was concluded that GO/Ni/Y‐MOFs exhibit a maximum adsorption capacity for tetracycline hydrochloride at pH 8, reaching up to 375.8 mg/g within 5 h. Overall, our results demonstrate that GO/Ni/Y‐MOFs are highly effective for the removal of tetracycline hydrochloride, both theoretically and experimentally.
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