Related Experiment Video
Updated: Jun 11, 2025

Ammonia Synthesis at Low Pressure
Published on: August 23, 2017
Recent Progress on Low-Temperature Selective Catalytic Reduction of NOx with Ammonia
1Department of Energy Systems Research, Ajou University, Suwon 16499, Republic of Korea.
Developing ammonia selective catalytic reduction (NH3-SCR) catalysts for low-temperature applications (<200 °C) is crucial for energy efficiency. Key factors include redox properties and surface acidity, with strategies to mitigate water and sulfur poisoning.
Area of Science:
- Environmental Science
- Catalysis
- Chemical Engineering
Background:
- Ammonia selective catalytic reduction (NH3-SCR) is vital for controlling nitrogen oxides (NOx) emissions from stationary and mobile sources at temperatures above 300 °C.
- Current NH3-SCR catalysts are less effective at lower temperatures (<200 °C), hindering energy efficiency and adaptability to diverse fuel sources.
Purpose of the Study:
- To systematically review recent advancements in low-temperature NH3-SCR catalysts.
- To identify key factors influencing catalytic activity and stability under low-temperature conditions.
Main Methods:
- Literature review of recent research on low-temperature NH3-SCR catalysts.
- Analysis of the role of redox properties and surface acidity in catalytic performance.
- Discussion of strategies to overcome challenges posed by water and sulfur oxides.
Main Results:
- Catalyst redox properties and surface acidity are critical for low-temperature NH3-SCR activity.
- Strong redox properties enhance activity but can lead to undesirable nitrous oxide (N2O) formation.
- Water and sulfur oxides (SOx) significantly inhibit NH3-SCR performance, particularly at low temperatures.
Conclusions:
- Optimizing redox properties through multiple electron transfer systems is promising for low-temperature NH3-SCR.
- Enhancing catalyst hydrophobicity can mitigate water interference.
- Developing robust catalysts resistant to SOx poisoning is essential for practical applications.
More Related Videos
07:14Automated, High-resolution Mobile Collection System for the Nitrogen Isotopic Analysis of NOx
Published on: December 20, 2016
08:05Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O
Published on: October 7, 2020
Related Concept Videos
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Preparation of Amines: Reduction of Amides and Nitriles
Amides can be reduced to primary, secondary, and tertiary amines using catalytic hydrogenation, active metals like Fe,...
Reduction of Alkynes to trans-Alkenes: Sodium in Liquid Ammonia
When dissolved in liquid ammonia, an alkali metal,...
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
Preparation of Amines: Alkylation of Ammonia and Amines
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...