Zhou Yanbo, Zhang Yongli, Hu Xiaomin
School of Resources and Civil Engineering, Northeastern University, Shenyang 110819, China.
School of Environment and Chemical Engineering, Foshan University, Foshan 528000, China.
J Colloid Interface Sci. 2020 Sep 1;575:206-219. doi: 10.1016/j.jcis.2020.04.024. Epub 2020 Apr 13.
Environment-friendly treatment process relies on the robustness, durability, and performance of catalysts to drive the development of cutting-edge sustainable technologies for the elimination of refractory contaminants. Herein, nanocomposites prepared from zero-valent Co-Fe encapsulated in nitrogen-containing carbon (NC) nanoparticles (CFNC-30 NPs) derived from CoFeO@zeolitic imidazolate frameworks-67 were successfully prepared through pyrolysis integrated with self-reduction, and further utilized as the novel catalysts to degrade 4-chlorophenol (4-CP) by coupling with peroxymonosulfate (PMS). Three optimized parameters (CFNC-30 NPs dosage of 0.089 g L, PMS concentration of 1.1 g L, and initial pH of 6.6) were obtained via response surface methodology by using the Box-Behnken design model. Benefiting from the larger specific surface area, pore-volume, and existence of abundant hydroxyl groups, CFNC-30 NPs with more available active sites exhibited an excellent efficiency of 99.1% toward catalytic degradation of 4-CP within 30 min under the optimal conditions. Moreover, CFNC-30 NPs demonstrated durability and long-term stability even during the five consecutive cycle tests without a significant drop in its catalytic performance. The scavenging experiments and electron paramagnetic resonance technologies revealed that non-radical singlet oxygen (O), sulfate radicals (SO), and hydroxyl radicals (HO) were involved as active species in the CFNC-30/PMS system, contributing 46.8, 35.6, and 17.6% efficiency toward 4-CP degradation, respectively. Besides, the reaction mechanism on the CFNC-30 NPs and degradation pathways toward 4-CP were speculated under PMS activation. The results indicated that the synergistic effects between zero-valent Co-Fe and NC structures not only significantly boosted the removal efficiency and long-term stability of CFNC-30 NPs, but also facilitated the redox cycles of Co/Co and Fe/Fe. This proof-of-concept approach to develop such high-efficient zero-valent Co-Fe encapsulated in NC structures opens up novel avenues for wastewater decontamination via PMS activation.
环境友好型处理工艺依赖于催化剂的稳健性、耐久性和性能,以推动用于消除难降解污染物的前沿可持续技术的发展。在此,通过热解与自还原相结合,成功制备了由包裹在含氮碳(NC)纳米颗粒(CFNC-30 NPs)中的零价Co-Fe制成的纳米复合材料,该纳米颗粒源自CoFeO@沸石咪唑酯骨架-67,并进一步用作新型催化剂,通过与过一硫酸盐(PMS)偶联来降解4-氯苯酚(4-CP)。使用Box-Behnken设计模型,通过响应面法获得了三个优化参数(CFNC-30 NPs剂量为0.089 g/L,PMS浓度为1.1 g/L,初始pH为6.6)。得益于更大的比表面积、孔体积以及大量羟基的存在,具有更多可用活性位点的CFNC-30 NPs在最佳条件下30分钟内对4-CP的催化降解效率高达99.1%。此外,即使在连续五次循环测试中,CFNC-30 NPs的催化性能也没有显著下降,表现出耐久性和长期稳定性。清除实验和电子顺磁共振技术表明,非自由基单线态氧(O)、硫酸根自由基(SO)和羟基自由基(HO)作为活性物种参与了CFNC-30/PMS体系,对4-CP降解的贡献效率分别为46.8%、35.6%和17.6%。此外,推测了CFNC-30 NPs上的反应机理以及4-CP的降解途径。结果表明,零价Co-Fe与NC结构之间的协同效应不仅显著提高了CFNC-30 NPs的去除效率和长期稳定性,还促进了Co/Co和Fe/Fe的氧化还原循环。这种开发包裹在NC结构中的高效零价Co-Fe的概念验证方法为通过PMS活化进行废水净化开辟了新途径。