Electrochemical recovery of H 2 and nutrients (N, P) from synthetic source separate urine water
This study examined an electrochemical method of H production and nutrient recovery from synthetic source separated urine (SSU). The efficacy of H production was examined through hydrogen recovery experiments (HRE) using Ni foam electrodes. Similarly, nutrient (N and P) recovery was also examined in...
Gespeichert in:
Veröffentlicht in: | Chemosphere (Oxford) 2021-04, Vol.269, p.129361 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | This study examined an electrochemical method of H
production and nutrient recovery from synthetic source separated urine (SSU). The efficacy of H
production was examined through hydrogen recovery experiments (HRE) using Ni foam electrodes. Similarly, nutrient (N and P) recovery was also examined in post-nutrient recovery experiments (NRE) with sacrificial Mg electrodes. To achieve higher nutrient recovery in the post-nutrient recovery process, the most important operating parameters (initial solution pH (pH
) and current density) were optimized. Optimization of NRE revealed that > 90% NH
-N and PO
-P could be recovered at 8 mA cm
with a pH
of 6-8. Notable NH
-N and PO
-P reduction were observed at an equimolar Mg
dissolution ratio (1:1) of Mg
:NH
and a 1.1:1 ratio of Mg
:PO
respectively. However, poor total Kjeldahl nitrogen (TKN) reduction was observed. Thus, we anticipate that direct electrochemical conversion of urea to N
at the anode followed by H
generation at the cathode is a more sustainable way to reduce TKN. Batch HRE showed that the initial TKN, 1094 mg L
(934 mg L
from urea-N and 160 mg L
from NH
Cl), was significantly reduced to 360 mg L
by Ni-Ni electrolysis, whereas around 53.8 g H
gas was received from this Ni-Ni electrolysis system with a flow rate of 5-5.8 g mol
day
. Overall, this work produced a 68% reduction in TKN due to electrochemical conversion of urea into H
. |
---|---|
ISSN: | 1879-1298 |
DOI: | 10.1016/j.chemosphere.2020.129361 |