Tailored Alkali Resistance of DeNOx Catalysts by Improving Redox Properties and Activating Adsorbed Reactive Species

It is still challenging to develop strongly alkali-resistant catalysts for selective catalytic reduction of NOx with NH3. It is generally believed that the maintenance of acidity is the most important factor because of neutral effects of alkali. This work discovers that the redox properties rather t...

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Veröffentlicht in:iScience 2020-06, Vol.23 (6), p.101173, Article 101173
Hauptverfasser: Khan, Mehak Nawaz, Han, Lupeng, Wang, Penglu, Zhang, Dengsong
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Sprache:eng
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Zusammenfassung:It is still challenging to develop strongly alkali-resistant catalysts for selective catalytic reduction of NOx with NH3. It is generally believed that the maintenance of acidity is the most important factor because of neutral effects of alkali. This work discovers that the redox properties rather than acidity play decisive roles in improving alkali resistance of some specific catalyst systems. K-poisoned Fe-decorated SO42−-modified CeZr oxide (Fe/SO42−/CeZr) catalysts show decreased acidity but reserve the high redox properties. The higher reactivity of NHx species induced by K poisoning compensates for the decreased amount of adsorbed NHx, leading to a desired reaction efficiency between adsorbed NHx and nitrate species. This study provides a unique perspective in designing an alkali-resistant deNOx catalyst via improving redox properties and activating the reactivities of NHx species rather than routinely increasing acidic sites for NHx adsorption, which is of significance for academic interests and practical applications. [Display omitted] •Fe-decorated SO42−-modified CeZr catalysts exhibit superior alkali resistance•Improved redox properties compensate for the loss of the acidity•Higher reactivity of NHx species makes up their decreased quantity•Alkali resistance is enhanced via improving the redox and reactivity of NHx species Chemical Engineering; Catalysis; Environmental Chemistry; Environmental Chemical Engineering
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2020.101173