Importance of water content in birnessite-type MnO2 catalysts for HCHO oxidation: Mechanistic details and DFT analysis

双锰矿 催化作用 化学 煅烧 格式化 氧气 无机化学 吸附 隐锰铁矿 化学工程 有机化学 工程类 氧化锰
作者
Changye Mang,Jun Luo,Cao Pengxu,Xin Zhang,Mingjun Rao,Guanghui Li,Tao Jiang
出处
期刊:Chemosphere [Elsevier BV]
卷期号:287: 132293-132293 被引量:10
标识
DOI:10.1016/j.chemosphere.2021.132293
摘要

Water is featured in an indispensable role during the process of catalytic oxidation of HCHO. In this work, a rich water-containing birnessite-type MnO 2 was synthesized, and its water content was adjusted through calcination. Phase structure and texture properties of the prepared birnessite were characterized. It was revealed that three types of water (namely absorbed water, molecular water, and structural hydroxyl) existed in birnessite. With the loss of water content, the interlayer distance of samples had decreased which changed the structure of birnessite to cryptomelane. This converted the morphology from an initial layered shape to a rod-like shape. Besides, the underlying mechanism for this effect on HCHO catalytic oxidation was elucidated. Results indicated that hydroxyl groups could slowly and sequentially oxidize HCHO to DOM, formate, and carbonate species. The hydroxyl groups also promoted the formation of oxygen vacancy which could activate O 2 to O− 2 and O − . The hydroxyl groups which were consumed had originally been supplied by the reaction between O- 2, O − , and H 2 O (absorbed and interlayer water in birnessite) which was then replenished from air stream. Clearly, water is favorable to the catalytic reaction. It is the main reason why birnessite can continuously decompose HCHO. • Hydroxyl groups can promote the formation of oxygen vacancy. • Water is a main reason to decompose HCHO continuously. • Loss of water will decrease K + ions and further cause lattice distortion. • Inadequate water brings imtermediate accumulated and impede the reaction.
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