School of Materials and Environmental Engineering, Shenzhen Polytechnic, Shenzhen 518055, China.
College of Chemical Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
Int J Environ Res Public Health. 2022 Dec 11;19(24):16651. doi: 10.3390/ijerph192416651.
In order to improve the catalytic activity and recycling performance of semiconductor activators, and improve the activation pathway of persulfate, graphitic carbon nitride (g-CN) was prepared by calcining melamine, and a composite activator AgO/g-CN based on g-CN supported metal oxide was prepared using a precipitation method. The morphology, structure, and basic properties of the composites were characterized using SEM, XRD, FT-IR and XPS. The activation efficiency of the AgO/g-CN composite activator on peroxodisulfate (PDS) was explored. The results showed that AgO in the composite activator was highly dispersed on the surface of g-CN and did not change the molecular structure of g-CN significantly. Under different activation systems, the degradation process of MO was best fitted under the pseudo-second-order reaction kinetic model, compared to the separate g-CN or AgO activated PDS systems; the activation of the PDS system with AgO/g-CN had the best effect on MO degradation; and the composite activator AgO/g-CN showed better activation performance. Under the conditions that the mass combined ratio of AgO in the activator was 12%, the initial concentration of PDS was 4 mmol/L, the initial concentration of the activator was 1.25 g/L, and the initial pH was 3, the degradation degree of MO reached 99.4% after 40 min reaction. The free radical quenching experiment proved that the active substances that could degrade MO in the system were SO· and ·OH, and the effect of SO· was greater than that of ·OH. The degradation degree of MO in the reaction system remained above 80% after four cycles of use, and the crystal structure of AgO/g-CN did not change significantly before and after the reaction. The above results show that AgO/g-CN is an efficient and stable composite activator with good application potential in the treatment of dye wastewater by activating PDS.
为提高半导体催化剂的催化活性和循环性能,改善过硫酸盐的活化途径,采用煅烧三聚氰胺的方法制备了石墨相氮化碳(g-CN),并采用沉淀法制备了基于负载金属氧化物的 g-CN 的复合活化剂 AgO/g-CN。采用 SEM、XRD、FT-IR 和 XPS 对复合材料的形貌、结构和基本性质进行了表征。探讨了 AgO/g-CN 复合活化剂对过一硫酸盐(PDS)的活化效率。结果表明,复合活化剂中的 AgO 高度分散在 g-CN 的表面,对 g-CN 的分子结构没有明显的改变。在不同的活化体系下,MO 的降解过程在拟二级反应动力学模型下拟合度最好,与单独的 g-CN 或 AgO 活化 PDS 体系相比;AgO/g-CN 活化 PDS 体系对 MO 降解的效果最好;复合活化剂 AgO/g-CN 表现出更好的活化性能。在活化剂中 AgO 的质量复合比为 12%、初始 PDS 浓度为 4mmol/L、初始活化剂浓度为 1.25g/L、初始 pH 值为 3 的条件下,反应 40min 后 MO 的降解度达到 99.4%。自由基猝灭实验证明,体系中能够降解 MO 的活性物质为 SO·和·OH,且 SO·的作用大于·OH。在 4 次循环使用后,反应体系中 MO 的降解度仍保持在 80%以上,AgO/g-CN 的晶体结构在反应前后没有明显变化。以上结果表明,AgO/g-CN 是一种高效稳定的复合活化剂,在活化 PDS 处理染料废水方面具有良好的应用潜力。