Related Experiment Video
Updated: Sep 8, 2025

Ammonia Synthesis at Low Pressure
Published on: August 23, 2017
N2/Ar Mixed Discharge for Efficient Nitrogen Activation toward Green Ammonia Synthesis Application
Souma Yoshida1, Naoya Murakami1, Keisuke Takashima2
1Kyushu Institute of Technology Graduate School of Life Science and Systems Engineering, Fukuoka 808-0196, Japan.
Abstract:
In ammonia synthesis, a new reaction system that does not use hydrogen (H2) as a raw material, such as the plasma/liquid (P/L) reaction, contributes to creating a sustainable chemical industry. The P/L reaction is intended to abstract hydrogen atoms from water molecules to synthesize ammonia under ambient conditions without any catalysts but using electrically activated nitrogen species in the plasma. Therefore, the energy transfer process leading to nitrogen activation is key to the P/L reaction. Argon-admixed nitrogen plasma can drastically alter nitrogen activation processes by energizing electrons and pooling energy into its excited states. This study examines the efficacy of activated nitrogen in N2/Ar mixed plasma and the lifetime of atomic nitrogen (Natom) produced in gaseous plasma. A qualitative assessment of the electron temperature using optical emission spectroscopy indicated that the argon admixture enhanced the electron collision reaction process and energy pooling. Quantification of Natom using vacuum ultraviolet spectroscopy revealed that argon admixture extended the apparent lifetime of Natom, thereby improving the transfer efficiency of activated nitrogen to the liquid surface for the P/L reaction and increased ammonia synthesis. Thus, this study contributes to the development of green synthetic processes of ammonia.
More Related Videos
Related Concept Videos
Inorganic Nitrogen Assimilation
Overview of Nitrogen Metabolism
The largest pool of nitrogen available in the terrestrial ecosystem is gaseous nitrogen (N2) from the air, but this...
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...
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 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism

