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由CoFeO@ZIF-67衍生的氮掺杂多孔碳纳米复合材料封装的新型零价钴铁,用于通过耦合过一硫酸盐促进4-氯苯酚的去除。

Novel zero-valent Co-Fe encapsulated in nitrogen-doped porous carbon nanocomposites derived from CoFeO@ZIF-67 for boosting 4-chlorophenol removal via coupling peroxymonosulfate.

作者信息

Zhou Yanbo, Zhang Yongli, Hu Xiaomin

机构信息

School of Resources and Civil Engineering, Northeastern University, Shenyang 110819, China.

School of Environment and Chemical Engineering, Foshan University, Foshan 528000, China.

出版信息

J Colloid Interface Sci. 2020 Sep 1;575:206-219. doi: 10.1016/j.jcis.2020.04.024. Epub 2020 Apr 13.

Abstract

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.

摘要

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。

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