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Electrochemical Ammonia Recovery from Anaerobic Centrate Using a Nickel-Functionalized Activated Carbon Membrane Electrode

48

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31

References

2021

Year

Abstract

Ammonia (NH<sub>3</sub>) recovery from used water (previously wastewater) is highly desirable to depart from fossil fuel-dependent NH<sub>3</sub> production and curb nitrogen emission to the environment. Electrochemical NH<sub>3</sub> recovery is promising since it can simply convert aqueous NH<sub>4</sub><sup>+</sup> to gaseous NH<sub>3</sub> using cathodic reactions (OH<sup>-</sup> generation). However, the use of a separated electrode and membrane imposes high resistances to the cathodic reaction and NH<sub>3</sub> transfer. This study examined an activated carbon (AC)-based membrane electrode functionalized with nickel to electrochemically recover NH<sub>3</sub> from synthetic anaerobic centrate. The membrane electrode was fabricated using nickel-adsorbed AC powder and a polyvinylidene fluoride (PVDF) binder, and the PVDF membrane layer was formed at the electrode surface by phase inversion. The NH<sub>3</sub>-N recovery flux of 50.3 ± 0.4 gNH<sub>3</sub>-N/m<sup>2</sup>/d was produced at 17.1 A/m<sup>2</sup> with a recovery solution at pH 7, and NH<sub>3</sub>-N fluxes and energy consumptions were improved as the recovery solution became acidic (62.2 ± 2.1 gNH<sub>3</sub>-N/m<sup>2</sup>/d with 16.0 ± 1.6 kWh/kgNH<sub>3</sub>-N at pH 2). Increasing PVDF loadings did not impact the electrochemical performances of the Ni/AC-PVDF electrode, but slightly lower (7%) NH<sub>3</sub>-N fluxes were obtained with higher PVDF loadings. Ni dissolution (3.7-6.0% loss) was affected by the recovery solution pH, but it did not impact the performances over the cycles.

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