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在模拟太阳光下,1D/2D γ-MnOOH-rGO 通过过一硫酸盐活化高效降解苯达松:性能和机理研究。

Efficient degradation of bentazone via peroxymonosulfate activation by 1D/2D γ-MnOOH-rGO under simulated sunlight: Performance and mechanism insight.

机构信息

School of Environmental Science and Engineering, Tianjin Key Lab of Biomass Waste Utilization, Tianjin University, Tianjin 300072, China.

Tianjin International Engineering Institute, Tianjin 300072, China.

出版信息

Sci Total Environ. 2020 Nov 1;741:140492. doi: 10.1016/j.scitotenv.2020.140492. Epub 2020 Jun 24.

Abstract

An innovative 1D/2D γ-MnOOH-rGO catalyst was successfully synthesized by anchoring γ-MnOOH nanowires on rGO nanosheets. Its catalytic activity was comprehensively evaluated by bentazone degradation in PMS/simulated sunlight system. Results showed that the γ-MnOOH-rGO catalyst achieved 96.1% decomposition of bentazone within 90 min in the coupled system, improving by 26.7% compared to that obtained in the γ-MnOOH mediated system. Moreover, the newly-designed γ-MnOOH-rGO exhibited stability, recyclability and practicability for bentazone elimination. Mechanism insight highlighted that more active sites exposed on γ-MnOOH-rGO surface, providing more opportunities for PMS activation and bentazone degradation. Besides, the rGO could transfer photo-induced electrons, accelerating radical-based reactions. More importantly, ∙OH and O appeared in γ-MnOOH-rGO/PMS/simulated sunlight system, which played an overwhelming role in bentazone removal. In prospect, the γ-MnOOH-rGO showed promising potential for refractory contaminants remediation from aquatic environment in PMS/photocatalytic system.

摘要

一种创新性的 1D/2D γ-MnOOH-rGO 催化剂通过将 γ-MnOOH 纳米线锚定在 rGO 纳米片上成功合成。通过 PMS/模拟太阳光系统中苯达松的降解来全面评估其催化活性。结果表明,在耦合体系中,γ-MnOOH-rGO 催化剂在 90 分钟内实现了苯达松的 96.1%分解,与 γ-MnOOH 介导体系相比提高了 26.7%。此外,新设计的 γ-MnOOH-rGO 表现出了苯达松去除的稳定性、可回收性和实用性。机理研究表明,γ-MnOOH-rGO 表面暴露了更多的活性位点,为 PMS 的活化和苯达松的降解提供了更多的机会。此外,rGO 可以转移光诱导电子,加速基于自由基的反应。更重要的是,γ-MnOOH-rGO/PMS/模拟太阳光系统中出现了 ∙OH 和 O,它们在苯达松的去除中起着至关重要的作用。展望未来,γ-MnOOH-rGO 在 PMS/光催化体系中对难降解污染物的修复具有广阔的应用前景。

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