Barrera A, Tzompantzi F, Campa-Molina J, Casillas J E, Pérez-Hernández R, Ulloa-Godinez S, Velásquez C, Arenas-Alatorre J
Laboratorio de Nanomateriales Catalíticos, Centro Universitario de la Ciénega, Universidad de Guadalajara, Av. Universidad No. 1115, Col. Linda Vista C.P. 47820 Ocotlán Jalisco México
Depto. de Química, Área de Catálisis, Universidad Autónoma Metropolitana - Iztapalapa Av. San Rafael Atlixco 189 C.P. 09340 Cd. de México México
RSC Adv. 2018 Jan 15;8(6):3108-3119. doi: 10.1039/c7ra12665d. eCollection 2018 Jan 12.
The photocatalytic activity in the degradation of 4-chlorophenol (4-ClPh) in aqueous medium (80 ppm) using 2.0 wt% Ag/AlO-GdO (Ag/Al-Gd-; where = 2.0, 5.0, 15.0, 25.0 and 50.0 wt% of GdO) photocatalysts prepared by the sol-gel method was studied under UV light irradiation. The photocatalysts were characterized by N physisorption, X-ray diffraction, SEM, HRTEM, UV-Vis, XPS, FTIR and fluorescence spectroscopy. About 67.0% of 4-ClPh was photoconverted after 4 h of UV light irradiation using Ag/γ--AlO. When Ag/Al-Gd- photocatalysts were tested, the 4-ClPh photoconversion was improved and more than 90.0% of 4-ClPh was photoconverted after 3 h of UV light irradiation in the materials containing 15.0 and 25.0 wt% of GdO. Ag/Al-Gd-25 was the material with the highest efficacy to mineralize dissolved organic carbon, mineralizing more than 85.0% after 4 h of UV light irradiation. Silver nanoparticles and micro-particles of irregular pentagonal shape intersected by plane nanobelts of AlO-GdO composite oxide were detected in the Ag/Al-Gd-25 photocatalyst. This material is characterized by a lowest recombination rate of electron-hole pairs. The low recombination rate of photo-induced electron-hole pairs in the Ag/Al-Gd- photocatalysts with high GdO contents (≥15.0 wt%) confirmes that the presence of silver nanoparticles and microparticles interacting with AlO-GdO composite oxide entities favors the separation of photo-induced charges (e and h). These materials could be appropriate to be used as highly efficient photocatalysts to eliminate high concentrations of 4-ClPh in aqueous medium.
采用溶胶 - 凝胶法制备了2.0 wt% Ag/AlO - GdO(Ag/Al - Gd - ;其中GdO的含量分别为2.0、5.0、15.0、25.0和50.0 wt%)光催化剂,并研究了其在紫外光照射下对水介质(80 ppm)中4 - 氯苯酚(4 - ClPh)的光催化降解活性。通过N物理吸附、X射线衍射、扫描电子显微镜(SEM)、高分辨率透射电子显微镜(HRTEM)、紫外 - 可见光谱、X射线光电子能谱(XPS)、傅里叶变换红外光谱(FTIR)和荧光光谱对光催化剂进行了表征。使用Ag/γ - AlO在紫外光照射4小时后,约67.0%的4 - ClPh发生了光转化。当测试Ag/Al - Gd - 光催化剂时,4 - ClPh的光转化得到改善,在含有15.0和25.0 wt% GdO的材料中,紫外光照射3小时后,超过90.0%的4 - ClPh发生了光转化。Ag/Al - Gd - 25是使溶解有机碳矿化效率最高的材料,紫外光照射4小时后矿化率超过85.0%。在Ag/Al - Gd - 25光催化剂中检测到银纳米颗粒和由AlO - GdO复合氧化物平面纳米带交叉的不规则五边形微粒。这种材料的特征是电子 - 空穴对的复合率最低。高GdO含量(≥15. wt%)的Ag/Al - Gd - 光催化剂中光致电子 - 空穴对的低复合率证实,银纳米颗粒和微粒与AlO - GdO复合氧化物实体的相互作用有利于光致电荷(e和h)的分离。这些材料适合用作高效光催化剂,以消除水介质中高浓度的4 - ClPh。