Simultaneous catalytic hydrolysis of HCN, COS and CS2 over metal-modified microwave coal-based activated carbon

被引:37
作者
Liu, Na [1 ]
Ning, Ping [1 ,3 ]
Sun, Xin [1 ]
Wang, Chi [2 ]
Song, Xin [1 ,3 ]
Wang, Fei [1 ]
Li, Kai [1 ,3 ]
机构
[1] Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Fac Chem Engn, Kunming 650500, Yunnan, Peoples R China
[3] Kunming Univ Sci & Technol, Natl Reg Engn Ctr Recovery Waste Gases Met & Chem, Kunming 650500, Yunnan, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Catalytic hydrolysis; HCN; COS and CS2; Al modified catalyst; Coal based activated carbon; SHELL; REMOVAL; OXIDATION; MECHANISM; SULFIDE;
D O I
10.1016/j.seppur.2020.118205
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this work, a series of metal oxides modified microwave coal-based activated carbon (MCAC) catalysts were prepared for simultaneously catalytic hydrolysis of hydrogen cyanide (HCN), carbonyl sulfide (COS) and carbon disulfide (CS2). The influences of metal species, precursor, metal oxides amount and calcination temperature were investigated. The interaction between Al2O3 and MCAC improved the dispersion of Al and enhanced the removal efficiency of catalyst. Al(2)O(3 )was the main active component and it provided the adsorption and hydrolysis abilities. The alkaline and strong oxidation sites were responsible for removing HCN, COS and CS2. Meanwhile, the adsorbed water was beneficial to the catalytic hydrolysis reactions. Al(2)O(3 )was attributed to the decomposition of aluminum salt. Under excessive high calcination temperature, Al(2)O(3 )reacted with surface functional groups. The formation of Al-2(SO4)(3) and Al(NO3)(3) resulted in the deactivation of catalyst.
引用
收藏
页数:9
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