通过光催化高效光降解药物的 ZnO 环保型合成方法

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Sharda Pandey*, Anchal Srivastava, Poonam Rawat, Satendra Kumar Chauhan, Anant Ram, Vishnu Kumar Diwedi, Rajesh Kumar Shukla and Navina Wadhwani, 
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引用次数: 0

摘要

本研究报告对分别用 3.17 和 4.17 M NaOH 合成氧化锌(ZnO)样品 1 和样品 2 的生态友好型进行了比较研究。使用紫外线(UV,280-400 nm)和 UV/H2O2 反应体系,将含有 4.17 M NaOH 的样品 2 用于对乙酰氨基酚(纯品和原料)的光催化降解。纯扑热息痛(PCM1)和来自药片的生扑热息痛(PCM2)被用于光催化降解。我们的实验证据表明,在光催化降解过程中,氧化锌样品 2 在紫外线/H2O2 反应体系中比仅在紫外线(UV,280-400 纳米)照射下更活跃。场发射扫描电子显微镜(FE-SEM)证实,样品 1 呈均匀生长的棒状结构,而样品 2 则呈脆性和随机聚集的棒状和线状纳米结构。在 250 °C 退火的样品 1 和样品 2 的傅立叶变换红外光谱中,在 440 至 900 cm-1 附近区域观察到的峰值证实了氧化锌键的存在。紫外吸收光谱显示,由于样品 2 中 NaOH 的摩尔浓度增加到 4.17 M,吸收光谱发生了红移。本研究发现,合成的 ZnO 样品 1 和样品 2 的带隙值分别为 3.33 和 3.01 eV,与块状 ZnO 的带隙值(3.37 eV)相比,分别减少了 40 和 360 meV。在 UV/H2O2 反应体系中,氧化速率增加,对 PCM1 药物的去除率最高,速率常数为 9.7 × 10-3 min-1,半衰期为 71.5 min。PCM1 和 PCM2 的去除动力学研究结果显示效果良好,并遵循伪一阶动力学模型,相关系数分别为 0.69556 和 0.90851,而 PCM2 则遵循伪二阶动力学模型,相关系数为 0.9993。在使用催化剂 ZnO 纳米结构去除对乙酰氨基酚的 PCM1 和 PCM2 时,发现平衡时去除能力(qe)的实验值和计算值与伪二阶动力学模型的值接近。ZnO 样品 2 的光稳定性也通过了至少四次对乙酰氨基酚光催化降解的可重复使用性测试。在 UV/H2O2 反应体系中,PCM1 在 243 处没有出现最大峰值,这表明使用合成的催化剂 ZnO 样品 2 几乎 100%地成功转化了 20 ppm 的 PCM1。紫外线和紫外线/H2O2 这两种反应体系的比较结果表明,羟基自由基作为活性物种,是两种扑热息痛形式(PCM1 和 PCM2)降解的主要原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eco-Friendly Synthesis of ZnO for Efficient Photodegradation of Pharmaceutical Drug Removal by Photocatalysis

In the present work, a comparative study on eco-friendly synthesis of zinc oxide (ZnO) sample 1 and sample 2 with 3.17 and 4.17 M NaOH, respectively, is reported. Sample 2 with 4.17 M NaOH is applied in the photocatalytic degradation of paracetamol (pure and raw both) using the ultraviolet (UV, 280–400 nm) and UV/H2O2 reaction systems. Pure paracetamol (PCM1) and raw paracetamol (PCM2) from tablets are used for photocatalytic degradation by photocatalysis. Our experimental evidence show that ZnO sample 2 was more active in the UV/H2O2 reaction system than under ultraviolet (UV, 280–400 nm) irradiation only in the photocatalytic degradation process. Field emission scanning electron microscopy (FE-SEM) confirms the homogeneous growth of a rod-like structure for sample 1 and brittle and randomly aggregated rod-like and wire-like nanostructures for sample 2. The peaks observed in the region around 440 to 900 cm–1 in the FTIR spectra for sample 1 and sample 2 annealed at 250 °C confirms the presence of ZnO bonds. UV absorption spectroscopy indicates a red shift in the absorption spectra due to the increase in the molar concentration of NaOH to 4.17 M for sample 2. In this study, the band gap values are found to be 3.33 and 3.01 eV for the synthesized ZnO sample 1 and sample 2, respectively, which are 40 and 360 meV less as compared to that of bulk ZnO (3.37 eV). The oxidation rate is increased in the UV/H2O2 reaction system, producing the highest rate for PCM1 drug removal with rate constant 9.7 × 10–3 min–1 and half-life 71.5 min. The kinetic study results for the removal of PCM1 and PCM2 show good results and follow the pseudo-first-order kinetic model with correlation coefficients 0.69556 and 0.90851, respectively, whereas PCM2 follows the pseudo-second-order kinetic model with correlation coefficient 0.9993. The experimental and calculated values of removal capacity (qe) at equilibrium is found close to those of the pseudo-second order kinetic model for the removal of both the paracetamol forms PCM1 and PCM2 with the catalyst ZnO nanostructure. The photostability of ZnO sample 2 is also tested with a reusability test in photocatalytic degradation of paracetamol at least four times. The absence of a maxima peak at 243 of PCM1 in the UV/H2O2 reaction system indicates nearly 100% successful conversion of 20 ppm PCM1 by using synthesized catalyst ZnO sample 2. The comparative results of both reaction systems, i.e., UV and UV/H2O2, show that the hydroxyl radicals, as the active species, are responsible for major degradation of both paracetamol forms (PCM1 and PCM2).

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CiteScore
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