Plasma-modified cerium oxide nanocatalyst for atmospheric pressure plasma degradation of methylene blue

被引:2
作者
Quezada-Urbina, Jesus [1 ,2 ]
Vazquez-Velez, Edna [1 ]
Martinez, Horacio [1 ]
Torres-Islas, Alvaro [2 ]
Huerta, Lazaro [3 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Ciencias Fis, Ave Univ S-N,Col Chamilpa, Cuernavaca 62210, Morelos, Mexico
[2] UAEMor, Fac Ciencias Quim Ingeniera FCQeI, Cuernavaca 62210, Morelos, Mexico
[3] Univ Nacl Autonoma Mexico, Inst Invest Mat, AP 70-360, Mexico City 04510, Mexico
关键词
Plasma; Photocatalyst; Degradation; Wastewater; CeO2; CEO2; PERFORMANCE; DRIVEN; XPS;
D O I
10.1016/j.jwpe.2024.105942
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel approach in the field of heterogeneous catalysis is presented in this research, focusing on organic compound degradation using CeO2. 2 . The catalyst was activated with plasma, producing active oxygen species from the water medium. CeO2 2 nanoparticles were synthesized using the chemical precipitation method and modified by a plasma treatment at atmospheric pressure. The untreated and plasma-treated nanostructures were analyzed using UV-VIS, Raman XRD, XPS spectroscopy, and TEM. The CeO2 2 Band Gap was modified with plasma from 3.31 eV to 2.85 eV. Raman and XRD spectroscopy found defects in the crystal lattice caused by oxygen vacancies, affecting the CeO2 2 surface reduction of Ce4+ 4 + to Ce3+. 3 + . XPS confirmed the Ce3+ 3 + content of 10 % to 18.5 % for untreated and plasma-treated CeO2, 2 , respectively. The percentage of degradation at 30 min was 50 % using plasma, 80 % in synergy with CeO2, 2 , and 90 % with CeO2 2 modified with plasma, indicating that the increase in degradation in the first minutes is due to the decomposition of H2O2 2 O 2 in their CeO2 2 active sites.
引用
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页数:11
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