Electrochemical determination of ammonia at low concentrations: detection of N2-electroreduction product in alkaline
Beata Rytelewska1, Anna Chmielnicka1, Takwa Chouki2
1University of Warsaw, Faculty of Chemistry, Pasteura 1, 02-093, Warsaw, Poland.
Abstract:
A catalytic system based on CeO2-supported Pt nanoparticles has been utilized and optimized to pursue electrochemical determination of ammonia (NH3) at fairly low concentrations (detection limit down to 2-3 μmol dm-3 level) through voltammetric oxidation of NH3 in alkaline medium (0.5 mol dm-3 NaOH). Dispersing and supporting of platinum nanoparticles on partially-defective and sub-stoichiometric ceria tends to increase the electrochemically active-surface-area and reproducibility of operation of the Pt-based catalyst. The approach has been found suitable to detect NH3 generated during electroreduction of nitrogen at Fe3P catalyst in the N2-saturated alkaline solution. Here the Pt-based "analytical" electrode has been utilized as the additional working electrode placed in the vicinity of the Fe3P-modified electrode. The analytical measurement does not require medium transfer to another solution because both Fe3P and Pt-based electrodes are operating in the sealed N2-electrolysis cell. Under such conditions, uncontrolled leakage and contamination by ammonia existing in the atmosphere can be avoided. The Pt-based electrode permits to perform blank experiments to comment about purity of electrolytes and nitrogen gas with respect to the presence of residual ammonia and the absence of oxygen and nitrogen oxides. Consequently, reliable determination of ammonia as the N2-electroreduction product following 2 h electrolysis at Fe3P iron phosphide catalyst becomes feasible. The results have been verified against spectrophotometric data. Formation of hydrazine or hydroxylamine as side (to ammonia) electroreduction products can be addressed by performing voltammetric diagnostic experiments with use of electrodes modified with Pt and Rh nanoparticles. Conversion of N2 to NH3 at Fe3P catalyst in 0.5 mol dm-3 NaOH is fairly selective because no appreciable amounts of hydrazine or hydroxylamine have been detected.
Related Concept Videos
Titration of a Weak Base with a Strong Acid
Using the ICE table and substituting the Kb value, we calculate the initial pH of 50 mL of 0.1 M ammonia to be 11.11. Addition of 25 mL of 0.1 M hydrochloric acid to this solution of ammonia results in a buffer with an equal concentration of ammonia and ammonium ions. The pH of this buffer can be calculated by substituting these...
Amperometry: Overview
Weak Base Solutions
Electrogravimetric Analysis: Overview
To test the completeness of the...
Titration of a Weak Acid with a Weak Base
As a result, there is no simple...
Controlled-Potential Coulometry: Electrolytic Methods
The chosen potential...


