Crystalline boron-boosted Fenton-like activation of persulfate by carbon-coated nano zero-valent iron for efficient degradation of tetracycline.

IF 9.7 1区 化学 Q1 CHEMISTRY, PHYSICAL
Song Li, Chen Chen, Jingshu Wang, Xiaoqing Min, Xinyue Xu
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引用次数: 0

Abstract

Nano zero-valent iron (nZVI)-based advanced oxidation processes (AOPs) have broad application prospects in environmental remediation, but the surface passivation of nZVI severely limits their performance. Although carbon coating can inhibit the oxidative passivation of nZVI in air, the deposition of iron ions on its surface during the reaction still leads to its rapid deactivation. In this study, crystalline boron was introduced as a novel co-catalyst to activate peroxydisulfate (PDS) in conjunction with carbon-coated nZVI (Fe0@C) for the degradation of tetracycline (TC). The results showed that the Boron/Fe0@C/PDS system achieved complete removal of TC within 1 min. Free radical scavenging and chemical probe experiments confirmed the generation of multiple reactive oxygen species, with singlet oxygen being primarily responsible for the degradation of TC. Mechanism investigations revealed that crystalline boron can accelerate the redox cycle of iron ions by donating electrons, thereby inhibiting the deposition of iron ions on the Fe0@C surface and achieving the stable release of ferrous ions and the continuous activation of PDS. Furthermore, crystalline boron gradually undergoes surface oxidation during the electron donation process, but its surface self-cleaning effect can continuously expose new active sites. The synergistic effect of crystalline boron and carbon coating prevents passivation of nZVI throughout its lifecycle, thereby ensuring excellent catalytic efficiency and long-term stability. This study provides a practical anti-passivation strategy and offers new insights into the rational design of nZVI-based AOPs.

碳包覆纳米零价铁催化过硫酸盐类fenton活化高效降解四环素。
基于纳米零价铁(nZVI)的高级氧化工艺(AOPs)在环境修复中具有广阔的应用前景,但nZVI的表面钝化严重限制了其性能。虽然碳涂层可以抑制nZVI在空气中的氧化钝化,但反应过程中铁离子在其表面的沉积仍然导致其快速失活。在这项研究中,晶体硼作为一种新的共催化剂,与碳包覆的nZVI (Fe0@C)一起激活过硫酸氢盐(PDS)降解四环素(TC)。结果表明,硼/Fe0@C/PDS体系可在1 min内完全去除TC。自由基清除和化学探针实验证实了多种活性氧的产生,其中单线态氧是降解TC的主要原因。机理研究表明,结晶硼可以通过提供电子加速铁离子的氧化还原循环,从而抑制铁离子在Fe0@C表面的沉积,实现亚铁离子的稳定释放和PDS的持续活化。此外,晶体硼在给电子过程中逐渐发生表面氧化,但其表面的自清洁作用可以不断暴露新的活性位点。结晶硼和碳涂层的协同作用防止了nZVI在整个生命周期内的钝化,从而保证了优异的催化效率和长期稳定性。该研究提供了一种实用的抗钝化策略,并为基于nzvi的AOPs的合理设计提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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