Catalytic performance of Ni-Doped Co/La2O3 for degradation of malachite green by hetero-Fenton-like oxidation and sonocatalysis processes

IF 4.7 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Structure Pub Date : 2025-06-15 Epub Date: 2025-02-09 DOI:10.1016/j.molstruc.2025.141612
Koubra Aribi , Madani Ghelamallah , Radia Imane Fertout , Farid Ait Merzeg , Atmane Djermoune
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Abstract

In this research, we investigated the performance of La2O3, Co/La2O3, and Ni-doped Co/La2O3 catalysts for the degradation of malachite green (MG), which is used as a model of wastewater refractory pollutants, under different reaction conditions (light irradiation or its absence, hetero-Fenton-like processes, without and with H2O2, and sonocatalytic degradation as intensifying energy). The catalysts were characterized using XRD, FTIR, and SEM-EDX. The results indicate that cobalt significantly influenced the microstructure and catalytic activity of the samples. The Ni-doped Co/La2O3 sample demonstrated a higher rate of catalytic degradation activity compared to the pure Co/La2O3 sample when reacting with H2O2. This degradation adhered to second-order and parabolic model reaction kinetics. Our kinetic studies revealed that at low initial concentrations of dye (8.22 × 10−5 M), the degradation efficiency over La2O3 by H2O2 exceeded 84.9 % (k = 0.4744 min-0.5) for the parabolic diffusion model R2 ≈ 1. The synergistic effect of sonocatalysis in the removal of MG increased the efficiency between 1.5 and 3.8 times. NiCo/La2O3 exhibited a better sonocatalytic degradation effect on the MG solution without and with H2O2, and the degradation reached 96.3 % (k = 0.5468 L.mg−1.min−1) within 40 min with R2 = 0.9812. The second-order and parabolic model described the experimental data well, and the reusability up to five cycles also showed no loss of catalytic activity. The obtained results are among the best reported in the literature for this reaction in comparison to related catalysts.

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ni掺杂Co/La2O3对异fenton -like氧化和声催化工艺降解孔雀石绿的催化性能
在本研究中,我们研究了La2O3, Co/La2O3和ni掺杂Co/La2O3催化剂在不同反应条件下(光照射或不照射,异质fenton -like过程,无H2O2和有H2O2,声催化降解作为强化能量)对孔雀石绿(MG)的降解性能,并将其作为废水难降解污染物的模型。采用XRD、FTIR和SEM-EDX对催化剂进行了表征。结果表明,钴对样品的微观结构和催化活性有显著影响。与纯Co/La2O3样品相比,ni掺杂Co/La2O3样品在与H2O2反应时表现出更高的催化降解活性。这种降解符合二级和抛物线模型反应动力学。动力学研究表明,在低初始染料浓度(8.22 × 10−5 M)下,对于抛物线扩散模型R2≈1,H2O2对La2O3的降解效率超过84.9% (k = 0.4744 min-0.5)。声催化的协同作用使MG的去除率提高了1.5 ~ 3.8倍。NiCo/La2O3对无H2O2和有H2O2的MG溶液均表现出较好的声催化降解效果,在40 min内降解率达到96.3% (k = 0.5468 L.mg−1.min−1),R2 = 0.9812。二阶和抛物线模型较好地描述了实验数据,并且重复使用高达5次循环也没有显示出催化活性的损失。与相关催化剂相比,所获得的结果是该反应文献中报道的最好的结果之一。
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来源期刊
Journal of Molecular Structure
Journal of Molecular Structure 化学-物理化学
CiteScore
7.10
自引率
15.80%
发文量
2384
审稿时长
45 days
期刊介绍: The Journal of Molecular Structure is dedicated to the publication of full-length articles and review papers, providing important new structural information on all types of chemical species including: • Stable and unstable molecules in all types of environments (vapour, molecular beam, liquid, solution, liquid crystal, solid state, matrix-isolated, surface-absorbed etc.) • Chemical intermediates • Molecules in excited states • Biological molecules • Polymers. The methods used may include any combination of spectroscopic and non-spectroscopic techniques, for example: • Infrared spectroscopy (mid, far, near) • Raman spectroscopy and non-linear Raman methods (CARS, etc.) • Electronic absorption spectroscopy • Optical rotatory dispersion and circular dichroism • Fluorescence and phosphorescence techniques • Electron spectroscopies (PES, XPS), EXAFS, etc. • Microwave spectroscopy • Electron diffraction • NMR and ESR spectroscopies • Mössbauer spectroscopy • X-ray crystallography • Charge Density Analyses • Computational Studies (supplementing experimental methods) We encourage publications combining theoretical and experimental approaches. The structural insights gained by the studies should be correlated with the properties, activity and/ or reactivity of the molecule under investigation and the relevance of this molecule and its implications should be discussed.
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