Yang Lin, Sun Yongxiang, Yu Ruiquan, Huang Pan, Zhou Qi, Yang Haoyu, Lin Shaojian, Zeng Hongbo
Department of Chemical and Materials Engineering, University of Alberta, Edmonton, AB T6G 1H9, Canada.
Guangdong Provincial Engineering Research Center for Urban Water Recycling and Environmental Safety, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, PR China.
J Hazard Mater. 2024 May 5;469:134101. doi: 10.1016/j.jhazmat.2024.134101. Epub 2024 Mar 20.
CO-responsive materials have emerged as promising adsorbents for the remediation of refractory organic dyes-contaminated wastewater without the formation of byproducts or causing secondary pollution. However, realizing the simultaneous adsorption-separation or complete removal of both anionic and cationic dyes, as well as achieving deeper insights into their adsorption mechanism, still remains a challenge for most reported CO-responsive materials. Herein, a novel type of urchin-like CO-responsive FeO microspheres (U-FeO @P) has been successfully fabricated to enable ultrafast, selective, and reversible adsorption of anionic dyes by utilizing CO as a triggering gas. Meanwhile, the CO-responsive U-FeO @P microspheres exhibit the capability to initiate Fenton degradation of non-adsorbable cationic dyes. Our findings reveal exceptionally rapid adsorption equilibrium, achieved within a mere 5 min, and an outstanding maximum adsorption capacity of 561.2 mg g for anionic dye methyl orange upon CO stimulation. Moreover, 99.8% of cationic dye methylene blue can be effectively degraded through the Fenton reaction. Furthermore, the long-term unresolved interaction mechanism of organic dyes with CO-responsive materials is deciphered through a comprehensive experimental and theoretical study by density functional theory. This work provides a novel paradigm and guidance for designing next-generation eco-friendly CO-responsive materials for highly efficient purification of complex dye-contaminated wastewater in environmental engineering.
一氧化碳响应性材料已成为用于修复难降解有机染料污染废水的有前景的吸附剂,不会形成副产物或造成二次污染。然而,对于大多数已报道的一氧化碳响应性材料而言,实现同时吸附分离或完全去除阴离子和阳离子染料,以及更深入地了解其吸附机制,仍然是一项挑战。在此,一种新型的海胆状一氧化碳响应性FeO微球(U-FeO@P)已成功制备出来,通过利用一氧化碳作为触发气体,实现对阴离子染料的超快、选择性和可逆吸附。同时,一氧化碳响应性U-FeO@P微球展现出引发对不可吸附阳离子染料进行芬顿降解的能力。我们的研究结果表明,在一氧化碳刺激下,阴离子染料甲基橙的吸附平衡异常迅速,仅在5分钟内即可达到,最大吸附容量高达561.2毫克/克。此外,99.8%的阳离子染料亚甲基蓝可通过芬顿反应有效降解。此外,通过密度泛函理论的综合实验和理论研究,破解了有机染料与一氧化碳响应性材料长期未解决的相互作用机制。这项工作为设计下一代环保型一氧化碳响应性材料提供了新的范例和指导,用于环境工程中高效净化复杂的染料污染废水。