Activation of peroxymonosulfate by morphologically modified NiCo2O4 and application to diclofenac degradation

Kanon Sampe , Hideyuki Katsumata , Ikki Tateishi , Mai Furukawa , Satoshi Kaneco
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Abstract

Water pollution caused by pharmaceutical wastewater is becoming increasingly serious. Diclofenac (DCF), a pharmaceutical compound widely used in many medicines, is an organic pollutant that poses potential risks to ecosystems and human health. In this study, a morphologically modified NiCo2O4 (NCO) catalyst was synthesized via a hydrothermal method and employed to activate peroxymonosulfate (PMS) for DCF degradation. As a result, 99.9 % of the DCF was successfully degraded within 10 min. It also succeeded in mineralizing 97.2 % of DCF after 10 min. Moreover, the NCO/PMS system was effective over a wide pH range. The degradation pathways involved both radical and non-radical mechanisms, with 1O2, SO4•–, and OH identified as the primary active species. In addition, the surface hydroxyl groups on the NCO are likely to play a significant role in the degradation process. This paper presents the development of a highly efficient catalyst for the degradation of organic pollutants using PMS.
改性NiCo2O4活化过氧单硫酸酯及其在双氯芬酸降解中的应用
制药废水对水体的污染日益严重。双氯芬酸(DCF)是一种有机污染物,对生态系统和人类健康构成潜在风险,是一种广泛应用于多种药物的药物化合物。本研究通过水热法合成了一种形态修饰的NiCo2O4 (NCO)催化剂,并利用该催化剂激活过氧单硫酸根(PMS)降解DCF。结果,99.9 %的DCF在10 min内被成功降解。在10 min后,DCF的矿化率为97.2% %。此外,NCO/PMS体系在较宽的pH范围内有效。降解途径包括自由基和非自由基两种机制,其中1O2、SO4•-和•OH是主要活性物质。此外,NCO表面的羟基可能在降解过程中发挥重要作用。本文介绍了PMS降解有机污染物的高效催化剂的研究进展。
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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