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 Nov;210:877-888. doi: 10.1016/j.chemosphere.2018.07.065. Epub 2018 Jul 17.
3D porous CoO/nitrogen-doped graphene aerogel (NGA) hybrid for heterogeneous activation of peroxymonosulfate (PMS) was prepared by feasible hydrothermal and freeze-drying methods. The morphology, crystal structure and chemical composition of the catalyst were investigated by scanning electron microscopy, X-ray diffractometer, X-ray photoelectron spectroscopy, Raman spectra and Fourier transform infrared spectroscopy. CoO/NGA at a high N doping level of 7.6% (in atomic percentage) exhibited excellent catalytic performance for acid orange 7 (AO7) degradation, with almost complete removal within 30 min. Moderate PMS content, higher temperature and lower solution pH conditions would facilitate the decomposition of AO7. The catalyst possesses excellent long-term stability and recycling performance with simple separation and post-treatment approaches. Kinetic model was developed to simulate the transformation of main active radical species and the AO7 oxidation profiles, considering effects of coexisting ions (Cl and HCO). Based on results of electron spin resonance, typical quenching tests and kinetic calculation, sulfate radicals play dominate role in AO7 degradation. CoO nanocrystals and the new active sites created by nitrogen doping into graphene honeycomb network should synergistically contribute to the high degradation efficiency. This work has expanded the possibility of recyclable catalysts design for heterogeneous activation of PMS, with a dual catalytically active center and desirable stability.
3D 多孔 CoO/氮掺杂石墨烯气凝胶(NGA)杂化材料通过可行的水热和冷冻干燥方法制备,用于过一硫酸盐(PMS)的非均相活化。通过扫描电子显微镜、X 射线衍射仪、X 射线光电子能谱、拉曼光谱和傅里叶变换红外光谱研究了催化剂的形态、晶体结构和化学成分。在高氮掺杂水平(原子百分比为 7.6%)下的 CoO/NGA 对酸性橙 7(AO7)降解表现出优异的催化性能,在 30 min 内几乎完全去除。适量的 PMS 含量、较高的温度和较低的溶液 pH 条件有利于 AO7 的分解。该催化剂具有出色的长期稳定性和可回收性能,采用简单的分离和后处理方法。通过开发动力学模型模拟主要活性自由基物种的转化和 AO7 的氧化曲线,考虑了共存离子(Cl 和 HCO)的影响。基于电子顺磁共振、典型的猝灭试验和动力学计算的结果,硫酸根自由基在 AO7 降解中起主导作用。CoO 纳米晶和氮掺杂到石墨烯蜂窝网络中形成的新活性位点应该协同作用,从而实现高降解效率。这项工作扩展了用于 PMS 非均相活化的可回收催化剂设计的可能性,具有双催化活性中心和理想的稳定性。