Fluorine-free strategy for hydroxylated Ti3C2/Ti3AlC2 catalysts with enhanced aerobic oxidative desulfurization and mechanism

催化作用 烟气脱硫 化学 氧气 蚀刻(微加工) 材料科学 基质(水族馆) 硫黄 环境友好型 无机化学 化学工程 图层(电子) 有机化学 工程类 地质学 海洋学 生物 生态学
作者
Qingxiao Zhang,Jing He,Xueli Fu,Songhai Xie,Runze Fan,Huirong Lai,Weihua Cheng,Peiyi Ji,Jie Sheng,Qingliang Liao,Wenshuai Zhu,Hui Li
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:430: 132950-132950 被引量:44
标识
DOI:10.1016/j.cej.2021.132950
摘要

Hydrofluoric acid is inevitable in most preparation schemes for two-dimensional MXene materials, which is dangerous and environmentally hazardous. Herein, hydroxylated Ti3C2/Ti3AlC2 (h-TC/TAC) catalysts were prepared via an alkaline etching process using a safer, more environmentally friendly alkali. After preferentially forming a hydroxylated Ti3C2 MXene layer on the surface of Ti3AlC2, Ti-C bonds on the surface were partially hydrolyzed, which exposed more active sites. Alkaline etching modulated the chemical composition and electronic structure of the catalyst surface, thus concentrating the active sites on the surface, which improved the activation efficiency and substrate conversion. For the aerobic oxidative desulfurization of a model fuel with a sulfur content of 220 ppm, the prepared catalyst exhibited a desulfurization rate of up to 99% when using air as a cheap molecular oxygen source. The enhanced activity of the h-TC/TAC catalyst was attributed to the continuous activation of molecular oxygen to form •OH and •O2–. Moreover, because the main structure of Ti3AlC2 was maintained, the catalyst could be recycled 8 times without a significant decrease in activity. This work not only shows the potential of alkaline etching for preparing MXene materials but also provides an important example of the thermocatalytic application of MXene and MAX phase materials.
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