Electrochemical Ammonia Recovery from Anaerobic Centrate Using a Nickel-Functionalized Activated Carbon Membrane Electrode.
Kyoung-Yeol KimDaniel A Moreno-JimenezHarry EfstathiadisPublished in: Environmental science & technology (2021)
Ammonia (NH3) recovery from used water (previously wastewater) is highly desirable to depart from fossil fuel-dependent NH3 production and curb nitrogen emission to the environment. Electrochemical NH3 recovery is promising since it can simply convert aqueous NH4+ to gaseous NH3 using cathodic reactions (OH- generation). However, the use of a separated electrode and membrane imposes high resistances to the cathodic reaction and NH3 transfer. This study examined an activated carbon (AC)-based membrane electrode functionalized with nickel to electrochemically recover NH3 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 NH3-N recovery flux of 50.3 ± 0.4 gNH3-N/m2/d was produced at 17.1 A/m2 with a recovery solution at pH 7, and NH3-N fluxes and energy consumptions were improved as the recovery solution became acidic (62.2 ± 2.1 gNH3-N/m2/d with 16.0 ± 1.6 kWh/kgNH3-N at pH 2). Increasing PVDF loadings did not impact the electrochemical performances of the Ni/AC-PVDF electrode, but slightly lower (7%) NH3-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.
Keyphrases
- room temperature
- ionic liquid
- perovskite solar cells
- carbon nanotubes
- solid state
- gold nanoparticles
- wastewater treatment
- microbial community
- molecularly imprinted
- metal organic framework
- magnetic resonance
- magnetic resonance imaging
- computed tomography
- mass spectrometry
- drinking water
- reduced graphene oxide
- high resolution
- amino acid