Provincial Key Laboratory of Oil & Gas Chemical Technology, College of Chemistry and Chemical Engineering, Northeast Petroleum University, Daqing, 163318, China; Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, Sun Yat-sen University, Guangzhou, 510275, China.
Provincial Key Laboratory of Oil & Gas Chemical Technology, College of Chemistry and Chemical Engineering, Northeast Petroleum University, Daqing, 163318, China.
Chemosphere. 2018 May;198:204-215. doi: 10.1016/j.chemosphere.2018.01.135. Epub 2018 Feb 3.
Cobalt-based heterogeneous catalyst has been recognized as one of most efficient activators for peroxymonosulfate (PMS) decomposition, but usually suffers from the poor stability and difficulty to recover and reuse. Here easily recyclable cobalt oxide (CoO) nanowires and nanoflowers grown on nickel foam (NF) are fabricated by a hydrothermal and calcination method. The prepared 3D CoO/NF catalyst is characterized and applied as a heterogeneous catalyst for PMS activation to generate sulfate radicals for decomposition of Acid Orange 7 (AO7). The results show that the AO7 degradation rate increases with cobalt loading and PMS dosage, but decreases with the increase of solution pH. The CoO/NF catalyst using 2 mM Co(NO)·6HO as cobalt source exhibits highest activity, and almost complete decolorization could be achieved within 30 min. The diverse effects of coexisting anions (SO, HCO, NO and Cl) on AO7 degradation are observed and explained. After 10 consecutive runs, excellent catalytic reactivity of the catalyst remains while the level of leached cobalt during the catalyst usage is much lower than the maximum allowable concentration in drinking and natural water. More importantly, the macroscopic CoO/NF catalyst shows advantage of easy recycling after application compared to traditional catalysts. It is believed that the as-prepared CoO/NF is promising to be an effective and green heterogeneous catalyst for PMS activation to degrade organic pollutants for environmental application.
钴基多相催化剂已被公认为过一硫酸盐(PMS)分解最有效的活化剂之一,但通常存在稳定性差、难以回收和重复使用的问题。本研究通过水热法和煅烧法制备了负载在泡沫镍(NF)上的可回收氧化钴(CoO)纳米线和纳米花。对制备的 3D CoO/NF 催化剂进行了表征,并将其作为多相催化剂应用于 PMS 活化以生成硫酸根自由基,用于分解酸性橙 7(AO7)。结果表明,AO7 的降解速率随钴负载量和 PMS 用量的增加而增加,但随溶液 pH 的增加而降低。以 2mM Co(NO)·6HO 为钴源的 CoO/NF 催化剂表现出最高的活性,在 30min 内几乎可以完全脱色。观察到并解释了共存阴离子(SO、HCO、NO 和 Cl)对 AO7 降解的多种影响。经过 10 次连续运行,催化剂仍保持良好的催化活性,而在催化剂使用过程中浸出的钴的水平远低于饮用水和天然水中的最大允许浓度。更重要的是,与传统催化剂相比,应用后的宏观 CoO/NF 催化剂在回收利用方面具有优势。研究表明,所制备的 CoO/NF 有望成为一种有效且绿色的 PMS 活化多相催化剂,用于降解环境应用中的有机污染物。