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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Selective catalytic reduction of NO with CH4 over cobalt-exchanged cage-based, small-pore zeolites with different framework structures
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Selective catalytic reduction of NO with CH4 over cobalt-exchanged cage-based, small-pore zeolites with different framework structures

机译:用不同框架结构的基于钴交换的笼式的小孔沸石的选择性催化还原NO.CH4

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摘要

Selective catalytic reduction of NO with CH4 (CH4-SCR) has been studied over divalent cobalt ions exchanged into four cage-based, small-pore zeolites with different framework topologies, i.e., Co-CHA, Co-RTH, Co-UFI, and Co-LTA with similar Si/Al and Co/Al ratios (10-11 and 0.44 - 0.49, respectively). The catalytic results obtained are compared with those of Co-ferrierite, one of the most active catalysts for this reaction. While the CH4-SCR activity of all zeolite-supported cobalt catalysts decreases under wet conditions, the activity of Co-CHA is least affected by water vapor, thereby outperforming Co-ferrierite. More interestingly, a decrease in Si/Al ratio of its support from 10 to 6 gave a NO conversion to N-2 of 90 % at 773 K under wet conditions. The overall characterization results of this study demonstrate that both the framework topology and composition of zeolite supports are critical factors determining the intrazeolitic Co2+ ion locations and thus their CH4-SCR activity.
机译:已经研究了用不同框架拓扑,即Cha,Co-Rth,Co-UFI和 具有类似Si / Al和Co / Al比率的Co-LTA(分别为10-11和0.44-0.49)。 将获得的催化结果与Co-Ferriere的催化结果相比,该反应的最活性催化剂之一。 虽然所有沸石负载的钴催化剂的CH4-SCR活性在潮湿条件下降低,但CO-CHA的活性受水蒸气的最小影响,从而优于富铁矿。 更有趣的是,在10至6中,其支持的Si / Al比的降低使得在潮湿条件下在773K下没有转化为90%的N-2。 本研究的总体表征结果表明,沸石支持的框架拓扑和组成是确定蛋白胶质二氧化碳+离子位置的关键因素,从而是它们的CH4-SCR活性。

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