TY - JOUR
T1 - Nickel-Based Membrane Electrodes Enable High-Rate Electrochemical Ammonia Recovery
AU - Hou, Dianxun
AU - Iddya, Arpita
AU - Chen, Xi
AU - Wang, Mengyuan
AU - Zhang, Wenli
AU - Ding, Yifu
AU - Jassby, David
AU - Ren, Zhiyong Jason
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We thank Xiangchen Huo (Colorado School of Mines) for her great assistance in membrane characterizations. We appreciate the financial support from the US Department of Agriculture (2017-67022-26135) and Office of Naval Research (N000141612210).
PY - 2018/6/25
Y1 - 2018/6/25
N2 - Wastewater contains significant amounts of nitrogen that can be recovered and valorized as fertilizers and chemicals. This study presents a new membrane electrode coupled with microbial electrolysis that demonstrates very efficient ammonia recovery from synthetic centrate. The process utilizes the electrical potential across electrodes to drive NH4+ ions toward the hydrophilic nickel top layer on a gas-stripping membrane cathode, which takes advantage of surface pH increase to realize spontaneous NH3 production and separation. Compared with a control configuration with conventionally separated electrode and hydrophobic membrane, the integrated membrane electrode showed 40% higher NH3-N recovery rate (36.2 ± 1.2 gNH3-N/m2/d) and 11% higher current density. The energy consumption was 1.61 ± 0.03 kWh/kgNH3-N, which was 20% lower than the control and 70-90% more efficient than competing electrochemical nitrogen recovery processes (5-12 kWh/kgNH3-N). Besides, the negative potential on membrane electrode repelled negatively charged organics and microbes thus reduced fouling. In addition to describing the system's performance, we explored the underlying mechanisms governing the reactions, which confirmed the viability of this process for efficient wastewater-ammonia recovery. Furthermore, the nickel-based membrane electrode showed excellent water entry pressure (¼41 kPa) without leakage, which was much higher than that of PTFE/PDMS-based cathodes (¼1.8 kPa). The membrane electrode also showed superb flexibility (180 ° bend) and can be easily fabricated at low cost (
AB - Wastewater contains significant amounts of nitrogen that can be recovered and valorized as fertilizers and chemicals. This study presents a new membrane electrode coupled with microbial electrolysis that demonstrates very efficient ammonia recovery from synthetic centrate. The process utilizes the electrical potential across electrodes to drive NH4+ ions toward the hydrophilic nickel top layer on a gas-stripping membrane cathode, which takes advantage of surface pH increase to realize spontaneous NH3 production and separation. Compared with a control configuration with conventionally separated electrode and hydrophobic membrane, the integrated membrane electrode showed 40% higher NH3-N recovery rate (36.2 ± 1.2 gNH3-N/m2/d) and 11% higher current density. The energy consumption was 1.61 ± 0.03 kWh/kgNH3-N, which was 20% lower than the control and 70-90% more efficient than competing electrochemical nitrogen recovery processes (5-12 kWh/kgNH3-N). Besides, the negative potential on membrane electrode repelled negatively charged organics and microbes thus reduced fouling. In addition to describing the system's performance, we explored the underlying mechanisms governing the reactions, which confirmed the viability of this process for efficient wastewater-ammonia recovery. Furthermore, the nickel-based membrane electrode showed excellent water entry pressure (¼41 kPa) without leakage, which was much higher than that of PTFE/PDMS-based cathodes (¼1.8 kPa). The membrane electrode also showed superb flexibility (180 ° bend) and can be easily fabricated at low cost (
UR - http://hdl.handle.net/10754/628230
UR - https://pubs.acs.org/doi/10.1021/acs.est.8b01349
UR - http://www.scopus.com/inward/record.url?scp=85049257168&partnerID=8YFLogxK
U2 - 10.1021/acs.est.8b01349
DO - 10.1021/acs.est.8b01349
M3 - Article
C2 - 29939725
SN - 0013-936X
VL - 52
SP - 8930
EP - 8938
JO - Environmental Science & Technology
JF - Environmental Science & Technology
IS - 15
ER -