光催化
锐钛矿
材料科学
曙红Y
傅里叶变换红外光谱
核化学
X射线光电子能谱
漫反射红外傅里叶变换
拉曼光谱
光降解
扫描电子显微镜
可见光谱
布鲁克特
化学
催化作用
化学工程
有机化学
复合材料
物理
光电子学
工程类
光学
作者
Alex T. Kuvarega,Rui W. M. Krause,Bhekie B. Mamba
摘要
Elimination of toxic organic compounds from wastewater is currently one of the most important subjects in water pollution control. Eosin Yellow, an anionic xanthene fluorescent dye, known to be carcinogenic, originates mainly from textile industrial processes and is resistant to conventional chemical or biological water treatment methods. Photocatalysis using non metal/platinum group metal-codoped TiO 2 may provide effective means of removing such dyes from contaminated water. In this study, nitrogen/palladium-codoped TiO 2 photocatalysts were prepared by calcination of the hydrolysis product of titanium isopropoxide, Ti(OC 3 H 7 ) 4, with aqueous ammonia. Samples were characterized by Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, thermogravimetric analysis (TGA), diffuse reflectance UV–vis spectrophotometry, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Anatase phase particles of size range 10–20 nm were confirmed by XRD, Raman, TEM, and SEM analysis. Codoping imparted a red shift in the absorption edges of the materials. Codoped TiO 2 showed greater photocatalytic Eosin Yellow degradation efficiency compared to singly doped N–TiO 2 or Pd–TiO 2 under visible light irradiation. The highest initial reaction rate of 2.238 × 10 –2 min –1 was observed for N/Pd–TiO 2 (0.8% Pd). The results demonstrated that the N/Pd-codoped TiO 2 (0.6% Pd) sample could completely degrade the dye in 3 h, while the commercial TiO 2, (Degussa P25) showed the lowest dye degradation efficiency.
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