Homogeneous Ni(I)tetra Sulfonated Phthalocyanine Electrocatalyst Generated at Low Overpotential Clubbed with a Wet‐Scrubbing Column for High Efficiency NO Reduction to NH 3

Although the degradation of NO gas to a less toxic form is a promising strategy to help solve atmospheric health and ozone depletion problems, conversion to a useful gas is a recent strategy. The generation of NH 3 from NO with high efficiency per catalyst area or weight is in the early stages. In t...

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Veröffentlicht in:ChemistrySelect (Weinheim) 2021-11, Vol.6 (43), p.11980-11984
Hauptverfasser: Muthuraman, G., Silambarasan, P., Moon, I.‐S.
Format: Artikel
Sprache:eng
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Zusammenfassung:Although the degradation of NO gas to a less toxic form is a promising strategy to help solve atmospheric health and ozone depletion problems, conversion to a useful gas is a recent strategy. The generation of NH 3 from NO with high efficiency per catalyst area or weight is in the early stages. In this investigation, a tetra sulfonated phthalocyanine with a Ni(II) (Ni(II)TSPc) complex was used to produce a low valent homogenous electrocatalyst Ni(I)TSPc in an alkaline medium at a lower overpotential. Ni(I)TSPc formation at a lower overpotential was demonstrated by the initial change in oxidation/reduction potential from 25 mV to −360 mV during electrolysis, peak potential change in cyclic voltammetry, and UV‐Vis spectral analysis. A potentiometric titration method used to quantify the electrogenerated Ni(I)TSPc revealed 90 % efficiency in 1 h. The decrease of Ni(I)TSPc concentration when contacting NO gas at the wet scrubber column showed that the NO removal process followed a Ni(I)TSPc (Ni(I)) mediation or mediated electrocatalytic reduction (MER) process. The NO removal efficiency reached almost 100 % at a 0.2 L/min gas flow rate of 20 ppm. The selective formation of NH 3 with a maximum of 1492 μmol/g Ni(I) was achieved for the first time in the homogeneous electrocatalytic reduction process. The developed process generated NH 3 from NO gas and has the potential for scale‐up.
ISSN:2365-6549
2365-6549
DOI:10.1002/slct.202103406