Catalytic hydrolysis of gaseous HCN over Cu–Ni/γ-Al₂O₃ catalyst: parameters and conditions

Abstract

 The Cu–Ni/γ-Al₂O₃ catalyst was prepared to study HCN hydrolysis

 On catalyst calcined at 400°C, the HCN removal efficiency reaches a maximum.

 HCN removal is the highest at 480 min at a H ₂ O/HCN volume ratio of 150

 The presence of CO facilitates HCN hydrolysis and increases NH ₃ production.

 O ₂ increases the HCN removal and NO_x production but decreases NH ₃ production

GRAPHIC ABSTRACT

To decompose efficiently hydrogen cyanide (HCN) in exhaust gas, g-Al₂O₃-supported bimetallic-based Cu–Ni catalyst was prepared by incipient-wetness impregnation method. The effects of the calcination temperature, H₂O/HCN volume ratio, reaction temperature, and the presence of CO or O₂ on the HCN removal efficiency on the Cu–Ni/g-Al₂O₃ catalyst were investigated. To examine further the efficiency of HCN hydrolysis, degradation products were analyzed. The results indicate that the HCN removal efficiency increases and then decreases with increasing calcination temperature and H₂O/HCN volume ratio. On catalyst calcined at 400°C, the efficiency reaches a maximum close to 99% at 480 min at a H₂O/HCN volume ratio of 150. The HCN removal efficiency increases with increasing reaction temperature within the range of 100°C–500°C and reaches a maximum at 500°C. This trend may be attributed to the endothermicity of HCN hydrolysis; increasing the temperature favors HCN hydrolysis. However, the removal efficiencies increases very few at 500°C compared with that at 400°C. To conserve energy in industrial operations, 400°C is deemed as the optimal reaction temperature. The presence of CO facilitates HCN hydrolysis andincreases NH₃ production. O₂ substantially increases the HCN removal efficiency and NO_x production but decreases NH₃ production.

Graphical abstract

Keywords

Hydrogen cyanide / Cu–Ni/g-Al₂O₃ / Catalytic hydrolysis

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Acknowledgements

This work is financially supported by the National Natural Science Foundation of China (Grant No. 21277064), and the Scientific Research Key Project Fund of Ministry of Education (No. 210202).

Funding

RIGHTS & PERMISSIONS

2016 Higher Education Press and Springer-Verlag Berlin Heidelberg