Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou, 510640, China; CAS Key Laboratory of Renewable Energy, Guangzhou, 510640, China; Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development, Guangzhou, 510640, China; Changzhou University, Changzhou, 213164, China.
Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou, 510640, China; CAS Key Laboratory of Renewable Energy, Guangzhou, 510640, China; Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development, Guangzhou, 510640, China.
Chemosphere. 2019 May;222:391-398. doi: 10.1016/j.chemosphere.2019.01.132. Epub 2019 Jan 24.
A series of TiO/biochar composite catalysts were prepared by the hydrolysis method for the degradation of methyl orange, where biochar was obtained from the pyrolysis of waste walnut shells. The catalysts were examined by scanning electron microscope (SEM), energy dispersive spectrometer (EDS), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), photoluminescence spectroscopy (PL) and X-ray photoelectron spectroscopy (XPS), elemental analysis and ultra violet-visible diffuse reflectance spectroscopy (UV-vis DRS). The photocatalytic activity results showed that the catalysts noted as CT0.1/1, CT0.2/2 and CT 0.5/1 exhibited higher catalytic activity than that of pure TiO. Besides, catalyst CT0.2/1 exhibited the highest catalytic activity (the decolorization efficiency of 96.88% and the mineralization efficiency of 83.23% were obtained), attributed to the synergistic effect of biochar and TiO, while CT1/1 possessed the lowest activity due to the shelter of light by the excess biochar. After 5 repeated use, the catalyst CT0.2/1 still exhibited rather high activity toward the degradation of MO, where the decolorization efficiency and mineralization efficiency of MO achieved 92.45% and 76.56%, and the loss of activity was negligible.
一系列的 TiO2/生物炭复合催化剂是通过水解法制备的,用于降解甲基橙,其中生物炭是由废核桃壳热解得到的。通过扫描电子显微镜 (SEM)、能谱仪 (EDS)、X 射线衍射 (XRD)、傅里叶变换红外光谱 (FTIR)、光致发光光谱 (PL)和 X 射线光电子能谱 (XPS)、元素分析和紫外可见漫反射光谱 (UV-vis DRS)对催化剂进行了研究。光催化活性结果表明,标记为 CT0.1/1、CT0.2/2 和 CT0.5/1 的催化剂比纯 TiO2 具有更高的催化活性。此外,催化剂 CT0.2/1 表现出最高的催化活性(获得了 96.88%的脱色效率和 83.23%的矿化效率),这归因于生物炭和 TiO2 的协同效应,而 CT1/1 由于过多的生物炭对光的遮蔽作用而表现出最低的活性。经过 5 次重复使用,催化剂 CT0.2/1 对 MO 的降解仍表现出相当高的活性,MO 的脱色效率和矿化效率分别达到 92.45%和 76.56%,活性损失可以忽略不计。