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壳聚糖衍生的 N 掺杂碳负载的 Cu/Fe 共掺杂 MoS 纳米粒子作为过一硫酸盐活化剂用于高效染料降解。

Chitosan-derived N-doped carbon supported Cu/Fe co-doped MoS nanoparticles as peroxymonosulfate activator for efficient dyes degradation.

机构信息

School of Chemical Engineering, Chongqing University of Technology, Chongqing 400054, China.

School of Chemical Engineering, Chongqing University of Technology, Chongqing 400054, China.

出版信息

Int J Biol Macromol. 2024 Oct;278(Pt 1):134352. doi: 10.1016/j.ijbiomac.2024.134352. Epub 2024 Jul 31.

DOI:10.1016/j.ijbiomac.2024.134352
PMID:39094868
Abstract

Peroxymonosulfate (PMS), which is dominated by free radical (SO) pathway, has a good removal effect on organic pollutants in complex water matrices. In this article, a new catalyst (CFM@NC) was synthesized by hydrothermal carbonization method with chitosan (CS) as N and C precursors, and used to activate PMS to degrade dye wastewater. CFM@NC/PMS system can degrade 50 mg·L rhodamine B by 99.59 % within 30 min, and the degradation rate remains as high as 97.32 % after 5 cycles. It has good complex background matrices, acid-base anti-interference ability (pH 2.6-10.1), universality and reusability. It can degrade methyl orange and methylene blue by >98 % within 30 min. The high efficiency of the composite is due to the fact that CS-modified MoS as a carrier exposes a large number of active sites, which not only disperses CuFeO nanoparticles and improves the stability of the catalyst, but also provides abundant electron rich groups, which promotes the activation of PMS and the production of reactive oxygen species (ROS). PMS is effectively activated by catalytic sites (Cu/Cu, Fe/Fe, Mo/Mo, pyridine N, pyrrole N, edge sulfur and hydroxyl group) to produce a large number of radicals to attack RhB molecules, causing chromophore cleavage, ring opening, and mineralization. Among them, free radical SO is the main ROS for RhB degradation. This work is expected to provide a new idea for the design and synthesis of environmentally friendly and efficient heterogeneous catalysts.

摘要

过一硫酸盐(PMS)主要通过自由基(SO)途径,对复杂水基质中的有机污染物具有良好的去除效果。本文采用水热碳化法以壳聚糖(CS)为 N 和 C 前体合成了一种新型催化剂(CFM@NC),并用于活化 PMS 降解染料废水。在 30 min 内,CFM@NC/PMS 体系可将 50mg·L 的罗丹明 B 降解 99.59%,经过 5 次循环后,降解率仍高达 97.32%。它具有良好的复杂背景基质、酸碱抗干扰能力(pH 2.6-10.1)、通用性和可重复使用性。它可以在 30 min 内将甲基橙和亚甲基蓝降解超过 98%。该复合材料的高效性归因于 CS 改性 MoS 作为载体暴露了大量的活性位点,这不仅分散了 CuFeO 纳米粒子并提高了催化剂的稳定性,而且提供了丰富的富电子基团,促进了 PMS 的活化和活性氧物质(ROS)的产生。催化位点(Cu/Cu、Fe/Fe、Mo/Mo、吡啶 N、吡咯 N、边缘硫和羟基)可有效激活 PMS 产生大量自由基攻击 RhB 分子,导致生色团断裂、开环和矿化。其中,自由基 SO 是 RhB 降解的主要 ROS。这项工作有望为设计和合成环保高效的多相催化剂提供新的思路。

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