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The NH3-SCR mechanism of a novel cerium-tungsten-titanium mixed oxide catalyst prepared through the hydrothermal co-precipitation method modified by H2O2 complex |
LIU Jing1, XIONG Zhi-bo1,2, ZHOU Fei1, JIN Jing1, LU Wei1, ZHANG Lei3 |
1. School of Energy and Power Engineering, University of Shanghai for Science & Technology, Shanghai 200093, China; 2. Key Laboratory of Flow Control and Simulation, University of Shanghai for Science & Technology, Shanghai 200093, China; 3. Huaneng Shandong Shidao Bay Nuclear Power Co. Ltd, Rongcheng 264312, China |
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Abstract Influence of H2O2 complex modification on the NH3-SCR Turnover Frequency (TOF) of cerium-tungsten-titanium mixed oxide catalyst prepared through the hydrothermal co-precipitation method was investigated. And the NH3-SCR mechanism for the catalyst modified by H2O2 complex was also studied by Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS). The results indicated that the intensity of Brønsted acid for mixed oxide was improved by H2O2 complex modification. Its low-temperature NH3 adsorption ability and low-medium temperature NH3-SCR activity were enhanced. The TOF value of NOx reduction at 400℃ was 0.658s-1 for the catalyst modified by H2O2 complex. There existed the competitive adsorption of NH3 and NOx on its surface. The NH3-SCR reaction was mainly the reaction between the adsorption of NH3 group (NH3, NH2 and NH4+) and the gaseous NOx on the surface of cerium-tungsten-titanium mixed oxide catalyst modified by H2O2 complex, and its low-temperature NH3-SCR mechanism obeys the Eley-Rideal mechanism.
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Received: 27 September 2017
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