Effect of pyrolysis, impregnation, and calcination conditions on the physicochemical properties of TiO2/Biochar composites intended for photocatalytic applications

生物炭 光催化 锐钛矿 煅烧 热解 材料科学 X射线光电子能谱 金红石 化学工程 生物量(生态学) 复合材料 傅里叶变换红外光谱 催化作用 化学 有机化学 海洋学 工程类 地质学
作者
Déyler Castilla-Caballero,Aracely Hernández‐Ramírez,Sofia Vázquez‐Rodríguez,José Colina–Márquez,Fiderman Machuca‐Martínez,Juan Barraza,Aicardo Roa-Espinosa,Astrid Medina-Guerrero,Sundaram Gunasekaran
出处
期刊:Journal of environmental chemical engineering [Elsevier]
卷期号:11 (3): 110274-110274 被引量:31
标识
DOI:10.1016/j.jece.2023.110274
摘要

Biochars are outstanding materials obtained from the pyrolysis of biomass, possessing unique physicochemical properties that are attractive for many environmental applications, including photocatalysis. In this work, we have synthesized for the first time TiO2/Biochar composites using Aeroxide P25 TiO2 and biochars produced from the thermal treatment at low (or null) oxygen content of Colombian coconut shells. To explore and ultimately tune the final physicochemical properties of the TiO2/Biochars materials, a facile wet impregnation method was assessed, in which the following factors were evaluated: 1) Temperature and 2) %O2 in the pyrolysis of the biomass, 3) TiO2/Biochar ratio used in the impregnation and 4) Calcination temperature of the TiO2/Biochar composites. A comprehensive characterization of the novel composites was done, using techniques such as: XRD, XPS, BET, ATR-FTIR, diffuse reflectance, PL, SEM, and electrochemical analysis. The material synthesized with TPyrol = 350 °C, %O2 = 2.5, T/B = 0.8 and TCal of 800 °C presented notable properties such as low Eg, reduced recombination of e--h+ pairs, a high surface area, and a relatively high photogeneration of charges, and interestingly, it experienced phase transition from Anatase-Rutile to Anatase-Brookite. On the other hand, low TPyrol and high %O2 values conduct to hydrophilic functional groups on the TiO2/Biochar composites, whereas the use of higher TPyrol and TCal lead to a more hydrophobic character but promote the reduction of the recombination of photogenerated e--h+ pairs. As a result, this information is relevant for planning future applications of photocatalysis for degrading pollutants of different chemical nature.
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