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用于通过光催化高效光降解去除药物的氧化锌的环保合成

Eco-Friendly Synthesis of ZnO for Efficient Photodegradation of Pharmaceutical Drug Removal by Photocatalysis.

作者信息

Pandey Sharda, Srivastava Anchal, Rawat Poonam, Chauhan Satendra Kumar, Ram Anant, Diwedi Vishnu Kumar, Shukla Rajesh Kumar, Wadhwani Navina

机构信息

Department of Physics, University of Lucknow, Lucknow, U.P. 226007, India.

Department of Chemistry, University of Lucknow, Lucknow, U.P. 226007, India.

出版信息

ACS Omega. 2024 Oct 30;9(45):45169-45189. doi: 10.1021/acsomega.4c06272. eCollection 2024 Nov 12.

Abstract

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/HO 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/HO 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 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/HO reaction system, producing the highest rate for PCM1 drug removal with rate constant 9.7 × 10 min 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 ( ) 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/HO 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/HO, show that the hydroxyl radicals, as the active species, are responsible for major degradation of both paracetamol forms (PCM1 and PCM2).

摘要

在本研究中,报道了分别用3.17 M和4.17 M NaOH对氧化锌(ZnO)样品1和样品2进行环保合成的对比研究。含4.17 M NaOH的样品2用于在紫外(UV,280 - 400 nm)和UV/HO反应体系中对扑热息痛(纯品和原料药)进行光催化降解。片剂中的纯扑热息痛(PCM1)和原料药扑热息痛(PCM2)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,ZnO样品2在UV/HO反应体系中比仅在紫外(UV,280 - 400 nm)照射下更具活性。场发射扫描电子显微镜(FE - SEM)证实样品1为棒状结构均匀生长,样品2为脆性且随机聚集的棒状和线状纳米结构。在250℃退火的样品1和样品2的傅里叶变换红外光谱(FTIR)中,在440至900 cm附近区域观察到的峰证实了ZnO键的存在。紫外吸收光谱表明,由于样品2中NaOH的摩尔浓度增加到4.17 M,吸收光谱发生红移。在本研究中,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(3.37 eV)相比分别低40和360 meV。在UV/HO反应体系中氧化速率增加,PCM1药物去除率最高,速率常数为9.7×10⁻³ min⁻¹,半衰期为71.5 min。去除PCM1和PCM2的动力学研究结果显示效果良好,分别遵循伪一级动力学模型,相关系数为0.69556和0.90851,而PCM2遵循伪二级动力学模型,相关系数为0.9993。对于两种扑热息痛形式PCM1和PCM2与催化剂ZnO纳米结构的去除,平衡时去除容量( )的实验值和计算值接近伪二级动力学模型的值。还通过至少四次扑热息痛光催化降解的可重复使用性测试对ZnO样品2的光稳定性进行了测试。在UV/HO反应体系中,PCM1在243处没有最大峰,这表明使用合成催化剂ZnO样品2可使20 ppm的PCM1几乎100%成功转化。两个反应体系(即UV和UV/HO)的对比结果表明,作为活性物种的羟基自由基是两种扑热息痛形式(PCM1和PCM2)主要降解的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e8/11561600/7736ad868b20/ao4c06272_0018.jpg

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