Loading…

Insights into the efficient removal and mechanism of NiFeAl-LDH with abundant hydroxyl to activate peroxymonosulfate for sulfamethoxazole wastewater

[Display omitted] •Ni2Fe0.25Al0.75-LDH with abundant hydroxyl groups was fabricated.•Ni2Fe0.25Al0.75-LDH/PMS system showed higher purification performance.•The presence of complexes and metal synergy was conducive to ROS formation.•The mechanism and the degradation pathway of SMX were proposed. Laye...

Full description

Saved in:
Bibliographic Details
Published in:Journal of colloid and interface science 2025-01, Vol.678 (Pt A), p.920-936
Main Authors: Liu, Siqi, Zhang, Jiajia, Hou, Xiangting, Bu, Wenqi, Lu, Shixu, Song, Xiaozhe, Zhou, Chengzhi, Wang, Qianwen, Xin, Shuaishuai, Liu, Guocheng, Xin, Yanjun, Yan, Qinghua
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:[Display omitted] •Ni2Fe0.25Al0.75-LDH with abundant hydroxyl groups was fabricated.•Ni2Fe0.25Al0.75-LDH/PMS system showed higher purification performance.•The presence of complexes and metal synergy was conducive to ROS formation.•The mechanism and the degradation pathway of SMX were proposed. Layered double hydroxide (LDH) material with abundant OH was successfully prepared by co-precipitation method, and a water purification system of Ni2Fe0.25Al0.75-LDH activated peroxymonosulfate (PMS) was constructed to rapidly degrade sulfamethoxazole (SMX) pollutants. The optimal conditions for the degradation of SMX in the system were as follows: 0.30 g/L Ni2Fe0.25Al0.75-LDH, 0.30 mM PMS, pH = 7 and 90 % SMX was removed in 10 min and almost completely in 40 min, which was consistent with the predicted results of response surface methodology (RSM) analysis. The abundant OH in Ni2Fe0.25Al0.75-LDH could form M(O)OSO3 complexes with PMS, accelerating the generation of reactive oxygen species (ROS) and promoting the removal of SMX. Quenching experiments and electron paramagnetic resonance (EPR) spectra showed that SO4−, OH, O2− and 1O2 also existed in the system. The surface-bound SO4− and O2− contributed greatly to the removal of SMX and the electron transfer between metals was also conducive to the production of active substances. The possible degradation pathways and intermediates of SMX were proposed. The toxicity assessment software tool (T.E.S.T) and total organic carbon (TOC) results indicated that the Ni2Fe0.25Al0.75-LDH/PMS system could reduce the overall environmental risk of SMX to some extent. This study provided a new strategy for the practical application of heterogeneous catalysts in sewage treatment.
ISSN:0021-9797
1095-7103
1095-7103
DOI:10.1016/j.jcis.2024.08.171