负载型铜铁催化剂直接催化分解N2O的研究

黄思齐, 王新承, 于泳, 徐庆生, 宋永吉, 李翠清, 王虹

现代化工 ›› 2019, Vol. 39 ›› Issue (8) : 124 -128,133.

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现代化工 ›› 2019, Vol. 39 ›› Issue (8) : 124-128,133. DOI: 10.16606/j.cnki.issn0253-4320.2019.08.026
科研与开发

负载型铜铁催化剂直接催化分解N2O的研究

    黄思齐, 王新承, 于泳, 徐庆生, 宋永吉, 李翠清, 王虹
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Study on direct catalytic decomposition of N2O by supported copper-iron catalyst

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摘要

利用等体积浸渍法制备了不同组成的CuFeO/γ-Al2O3复合氧化物催化剂,通过催化分解N2O的活性评价结果确定催化剂的最佳Cu-Fe原子质量比为2∶1、最佳负载量为25%。通过XRD、BET、H2-TPR等表征手段对催化剂的结构进行研究。结果表明,Cu2Fe1O/γ-Al2O3催化剂表面的CuO结晶度较小且高度分散,具有较大的比表面积;相比其他CuFeO/γ-Al2O3复合氧化物催化剂和单组分CuO/γ-Al2O3催化剂,Cu2Fe1O/γ-Al2O3还原能力更强,故表现出更强的N2O催化分解能力。考察了N2O质量分数、O2体积分数、空速等反应条件对Cu2Fe1O/γ-Al2O3活性的影响。在515℃高温条件下连续反应100 h,N2O转化率保持在90%左右,表明Cu2Fe1O/γ-Al2O3催化剂具有良好的热稳定性。

Abstract

A group of CuFeO/γ-Al2O3 composite oxides catalysts with different compositions are prepared by equal volume impregnation method.The best Cu-Fe atomic ratio in catalyst is determined as 2:1 and the optimal loading amount is 25% through activity evaluation in catalytic decomposition of N2O.The structure of the catalyst is studied by means of XRD,BET and H2-TPR characterization methods.Study results illustrate that CuO crystal on the surface of Cu2Fe1O/γ-Al2O3 catalyst is small,highly dispersed,and has a large specific surface area;Compared with other CuFeO/γ-Al2O3 composite oxide catalysts and CuO/γ-Al2O3 catalysts,Cu2Fe1O/γ-Al2O3 has stronger reducing ability,so it exhibits stronger ability in catalytic decomposition of N2O.Effects of several reaction conditions on the activity of Cu2Fe1O/γ-Al2O3 are studied,including the mass fraction of N2O,the volume fraction of O2 and space velocity.The conversion of N2O over Cu2Fe1O/γ-Al2O3 keeps at 90% in 100 h of continuous reaction at 515℃,indicating that Cu2Fe1O/γ-Al2O3 catalyst has a good thermal stability.

关键词

氧化亚氮 / 催化性能 / Cu-Fe复合氧化物 / 催化分解 / 等体积浸渍

Key words

nitrous oxide / catalytic performance / Cu-Fe composite oxides / catalytic decomposition / equal volume impregnation

Author summay

黄思齐(1994-),男,硕士研究生,研究方向为工业催化减排,945107635@qq.com

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负载型铜铁催化剂直接催化分解N2O的研究[J]. 现代化工, 2019, 39(8): 124-128,133 DOI:10.16606/j.cnki.issn0253-4320.2019.08.026

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