Interconversion and Removal of Inorganic Nitrogen Compounds via UV Irradiation

Author:

Senn Alejandro M.1,Quici Natalia12ORCID

Affiliation:

1. División Química de la Remediación Ambiental, Centro Atómico Constituyentes, CNEA, CONICET, Gral. Paz 1499, San Martín, Buenos Aires 1650, Argentina

2. Centro de Tecnologías Químicas, Departamento de Ingeniería Química, FRBA-UTN, Buenos Aires 1041, Argentina

Abstract

Dissolved inorganic nitrogen (DIN) species are key components of the nitrogen cycle and are the main nitrogen pollutants in groundwater. This study investigated the interconversion and removal of the principal DIN compounds (NO3−, NO2− and NH4+) via UV light irradiation using a medium-pressure mercury lamp. The experiments were carried out systematically at relatively low nitrogen concentrations (1.5 mM) at varying pHs in the presence and absence of oxygen to compare the reaction rates and suggest the reaction mechanisms. NO3− was fully converted into NO2− at a pH > 3 in both oxic and anoxic conditions, and the reaction was faster when the pH was increased following a first-order kinetic at pH 11 (k = 0.12 min−1, R2 = 0.9995). NO2− was partially converted into NO3− only at pH 3 and in the presence of oxygen and was stable at an alkaline pH. This interconversion of NO3− and NO2− did not yield nitrogen loss in the solution. The addition of formic acid as an electron donor led to the reduction of NO3− to NH4+. Conversely, NH4+ was converted into NO2−, NO3− and to an unidentified subproduct in the presence of O2  at pH 10. Finally, it was demonstrated that NO2− and NH4+ react via UV irradiation with stoichiometry 1:1 at pH 10 with the total loss of nitrogen in the solution. With these results, a strategy to remove DIN compounds via UV irradiation was proposed with the eventual use of solar light.

Funder

Agencia Nacional de Promoción Científica y Tecnológica

Consejo Nacional de Investigaciones Científicas y Técnicas

Publisher

MDPI AG

Subject

General Energy,General Engineering,General Chemical Engineering

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