Electrokinetics of Nitrite to Ammonia Conversion in the Neutral Medium Over A Platinum Surface.

Chem Asian J

Electrochemistry & Catalysis Research Laboratory (ECRL), Department of Chemistry, School of Physical Sciences, Shahjalal University of Science and Technology, Sylhet, 3114, Bangladesh.

Published: October 2024

AI Article Synopsis

  • A polycrystalline platinum (Pt) electrode was used to convert nitrite ions into nitrogen compounds through electrochemical reduction in a neutral environment.
  • The reduction produced nitric oxide (NO) and ammonia (NH₃), suggesting a transformation of NO into NH₃ during the process, confirmed by various analytical techniques.
  • Kinetic studies indicated that the reduction of nitrite ions to NO is an irreversible reaction dependent on ion diffusion, with a formal reduction potential of -0.46 V and an activation energy of approximately 19.8 kJ/mol.

Article Abstract

Polycrystalline Pt electrode was employed to selectively convert nitrite ions ( ) into useful nitrogenous compound through electrochemical reduction reaction in neutral medium. According to adsorptive stripping analysis, the reduction process produced nitric oxide (NO) on the surface of Pt electrode. The spectroscopic test and gas chromatographic studies discovered the presence of ammonia (NH) in the electrolyzed solution, suggesting the transformation of adsorbed NO into NH during the reverse scan. Scan rate dependent investigation was performed to elucidate kinetic information relating to this reaction on Pt surface. From E vs scan rate (υ) and j vs υ (logarithmic plot), it was found that the conversion of ion into NO is an irreversible reaction which relies on the diffusion of ions to electrode surface. The Tafel analysis unveiled that the first electron transfer sets the overall reaction rate, having formal reduction potential, E'=-0.46 V and standard heterogeneous rate constant, k= cm s. Reductive transfer coefficient (α) is another kinetics parameter, which was found to be approximate 0.77 from the difference between E and E of the voltammograms obtained over scan rate range 0.005 V s to 0.250 V s, indicating a stepwise process. According to temperature-dependent voltammograms, the nitrite reduction reaction on Pt had a calculated activation energy of about 19.8 kJ mol and a pre-exponential factor of about 8.39×10 mA cm.

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Source
http://dx.doi.org/10.1002/asia.202400362DOI Listing

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