Suppression of Ammonia Slip by Smart Reductants in Selective Catalytic Reduction of Nitrogen Oxides

X Xiaoya Xue (Innovation Institute of Carbon Neutrality International Joint Laboratory of Catalytic Chemistry College of Sciences State Key Laboratory of Materials for Advanced Nuclear Energy Shanghai University Shanghai China) A Aling Chen (Innovation Institute of Carbon Neutrality International Joint Laboratory of Catalytic Chemistry College of Sciences State Key Laboratory of Materials for Advanced Nuclear Energy Shanghai University Shanghai China) J Jun Liu M Mzamo Shozi (Discipline of Chemistry School of Agriculture and Science University of KwaZulu‐Natal Durban South Africa) X Xiaonan Hu (Innovation Institute of Carbon Neutrality, International Joint Laboratory of Catalytic Chemistry, State Key Laboratory of Materials for Advanced Nuclear Energy, Department of Chemistry, College of Sciences) F Fuli Wang (State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering) M Ming Xie (Department of Chemical Engineering) W Wenqiang Qu (University of Toronto , , 80 St. George Street , , ,) J Jiang Deng (Innovation Institute of Carbon Neutrality, International Joint Laboratory of Catalytic Chemistry, State Key Laboratory of Materials for Advanced Nuclear Energy, Department of Chemistry, College of Sciences) D Dengsong Zhang (Shanghai University , , ,)

Abstract

ABSTRACT Ammonia (NH 3 )‐based selective catalytic reduction (SCR) is a mainstream flue gas denitration technology for stationary and mobile sources, but NH 3 slip remains a critical challenge from mismatches between stoichiometric reaction requirements and fluctuating nitrogen oxides (NO x ) concentrations. Herein, we show organic amines (e.g., n ‐butylamine, n ‐B) act as smart reductants for SCR systems. Unlike NH 3 , n ‐B reacts stoichiometrically with NO x and undergoes NO‐accelerated self‐elimination when overdosed over TiO 2 ‐supported VO x catalysts. Mechanistic studies reveal Ti─OH sites on the catalyst facilitate n ‐B adsorption and activation, with the *NH 3 intermediate driving NO x reduction. *NH 2 from excess n ‐B oxidizes to nitrites and NO 2 under NO+O 2 , which further react with *NH 3 via an internal SCR pathway, avoiding free NH 3 formation and slip. We propose a hybrid reductants system (NH 3 + n ‐B) enabling efficient NH 3 slip suppression over a reductant/NO x molar ratio of 1.2, providing a promising strategy without modifying existing SCR hardware or structures.

Article Details

Volume / Issue Vol. 65, Issue 27
Published July 01, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

X

Xiaoya Xue

Innovation Institute of Carbon Neutrality International Joint Laboratory of Catalytic Chemistry College of Sciences State Key Laboratory of Materials for Advanced Nuclear Energy Shanghai University Shanghai China

A

Aling Chen

Innovation Institute of Carbon Neutrality International Joint Laboratory of Catalytic Chemistry College of Sciences State Key Laboratory of Materials for Advanced Nuclear Energy Shanghai University Shanghai China

J

Jun Liu

M

Mzamo Shozi

Discipline of Chemistry School of Agriculture and Science University of KwaZulu‐Natal Durban South Africa

X

Xiaonan Hu

Innovation Institute of Carbon Neutrality, International Joint Laboratory of Catalytic Chemistry, State Key Laboratory of Materials for Advanced Nuclear Energy, Department of Chemistry, College of Sciences

F

Fuli Wang

State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering

M

Ming Xie

Department of Chemical Engineering

W

Wenqiang Qu

University of Toronto , , 80 St. George Street , , ,

J

Jiang Deng

Innovation Institute of Carbon Neutrality, International Joint Laboratory of Catalytic Chemistry, State Key Laboratory of Materials for Advanced Nuclear Energy, Department of Chemistry, College of Sciences

D

Dengsong Zhang

Shanghai University , , ,