Related Experiment Video
Updated: Jan 3, 2026

Synthesis and Characterization of Fe-doped Aluminosilicate Nanotubes with Enhanced Electron Conductive Properties
Published on: November 15, 2016
Alkali-Poisoning-Resistant Fe2O3/MoO3/TiO2 Catalyst for the Selective Reduction of NO by NH3: The Role of the MoO3
Jie Zhang1, Zhiwei Huang1, Yueyao Du1
1Department of Environmental Science & Engineering, Huaqiao University, Xiamen 361021, P. R. China.
Abstract:
The exhaust gas contains harmful products, including fuel-additive elements such as compounds of sodium, which cause dramatic catalyst deactivation of catalysts during selective catalytic reduction (SCR) of NO with NH3. There is an increasing demand to synthesize alkali-poisoning-resistant catalysts for industrial NH3-SCR applications. In this study, the as-synthesized Fe2O3/MoO3/TiO2 exhibits a high degree of resistance toward Na2SO4 poisoning during the NH3-SCR reaction. With 500 μmol g-1 Na+ poisoning, Fe2O3/MoO3/TiO2 showed approximately 95% (or more) of its original activity throughout the entire temperature rage. Even with 700 μmol g-1 Na+ poisoning, Fe2O3/MoO3/TiO2 still performed well. The 500 and 700 μmol g-1 Na+ loadings dictate that, on average, SCR catalysts could be exposed to alkali-rich and highly dusty environments for more than 14 000 and 20 000 h, respectively. The layered MoO3 building block is used as a binding buffer and sandwiched between the active phase and TiO2 support to provide sufficiently stable binding sites for Na2SO4 poison and to present alkali blocking of the surface active phase. Our findings provide useful information regarding the use of MoO3 as a safety buffer for developing functional NH3-SCR catalysts with enhanced alkali-poisoning-resistant performance and long lifetimes.
More Related Videos
08:13Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area
Published on: February 19, 2018
06:00Solvothermal Synthesis of MIL-96 and UiO-66-NH2 on Atomic Layer Deposited Metal Oxide Coatings on Fiber Mats
Published on: June 13, 2018
Related Concept Videos
Redox Titration: Other Oxidizing and Reducing Agents
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,...
Radical Oxidation of Allylic and Benzylic Alcohols
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
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: Reductive Amination of Aldehydes and Ketones