Catalytic Ozonation of Quinoline Utilizing Manganese-Based Catalyst with Abundant Oxygen Vacancies

被引:11
|
作者
Xia, Liquan [1 ,2 ,3 ]
Liang, Wenhui [4 ]
Chen, Guifeng [2 ,3 ]
Li, Wenbo [2 ,3 ]
Gao, Minglong [2 ,3 ]
机构
[1] China Coal Res Inst, Beijing 100013, Peoples R China
[2] China Coal Res Inst Co Ltd, Beijing 100013, Peoples R China
[3] State Key Lab Coal Min & Clean Utilizat, Beijing 100013, Peoples R China
[4] Jiangsu Second Normal Univ, Coll Life Sci & Chem, Nanjing 210013, Peoples R China
基金
国家重点研发计划;
关键词
Precursor; MnO2; Oxygen vacancy; Catalytic oxidation; Quinoline; GASIFICATION WASTE-WATER; DEGRADATION; OXIDE; MNO2; MECHANISMS; REMOVAL;
D O I
10.1007/s10562-021-03735-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
S-MnO2, Cl-MnO2, and Ac-MnO2 samples were prepared by redox method with the oxidant (KMnO4) and the reducing agent precursors [MnSO4, MnCl2 and Mn(Ac)(2)]. This work studied the influence of the precursors on the catalytic performance. Ac-MnO2 was aminated and doped with graphene to obtain the modified manganese-based catalyst MnO2-NH2-GO. XRD, Raman, FTIR, XPS, NH3-TPD, CV (cyclic voltammetry) were used to characterize the catalyst. The average oxidation state (AOS) of Mn element was also calculated. The results of the catalytic ozonation quinoline degradation experiment shown that the four catalysts was ranked as follows: S-MnO2 < Cl-MnO2 < Ac-MnO2 < MnO2-NH2-GO, which was related to the catalyst crystal structure, oxygen vacancy (O-vac)content, AOS, and catalyst surface acidity and other factors. The effects of CO32-, HCO3-, SO42-, and Cl- on the catalytic reaction were investigated, the effects of different anions vary greatly. By adding tertiary butyl alcohol (tBA) and benzoquinone (pBQ) radical scavengers, it was confirmed that OH and O-2(-) coexisted, but O-2(-) contributed much more to oxidation than OH. Graphic Abstract
引用
收藏
页码:1669 / 1677
页数:9
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