TY - JOUR
T1 - Hydrogen production from inexhaustible supplies of fresh and salt water using microbial reverse-electrodialysis electrolysis cells
AU - Kim, Y.
AU - Logan, B. E.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): KUS-I1-003-13
Acknowledgements: This research was supported by funding through the King Abdullah University of Science and Technology (KAUST) (Award KUS-I1-003-13).
This publication acknowledges KAUST support, but has no KAUST affiliated authors.
PY - 2011/9/19
Y1 - 2011/9/19
N2 - There is a tremendous source of entropic energy available from the salinity difference between river water and seawater, but this energy has yet to be efficiently captured and stored. Here we demonstrate that H(2) can be produced in a single process by capturing the salinity driven energy along with organic matter degradation using exoelectrogenic bacteria. Only five pairs of seawater and river water cells were sandwiched between an anode, containing exoelectrogenic bacteria, and a cathode, forming a microbial reverse-electrodialysis electrolysis cell. Exoelectrogens added an electrical potential from acetate oxidation and reduced the anode overpotential, while the reverse electrodialysis stack contributed 0.5-0.6 V at a salinity ratio (seawater:river water) of 50. The H(2) production rate increased from 0.8 to 1.6 m(3)-H(2)/m(3)-anolyte/day for seawater and river water flow rates ranging from 0.1 to 0.8 mL/ min. H(2) recovery, the ratio of electrons used for H(2) evolution to electrons released by substrate oxidation, ranged from 72% to 86%. Energy efficiencies, calculated from changes in salinities and the loss of organic matter, were 58% to 64%. By using a relatively small reverse electrodialysis stack (11 membranes), only ~1% of the produced energy was needed for pumping water. Although Pt was used on the cathode in these tests, additional tests with a nonprecious metal catalyst (MoS(2)) demonstrated H(2) production at a rate of 0.8 m(3)/m(3)/d and an energy efficiency of 51%. These results show that pure H(2) gas can efficiently be produced from virtually limitless supplies of seawater and river water, and biodegradable organic matter.
AB - There is a tremendous source of entropic energy available from the salinity difference between river water and seawater, but this energy has yet to be efficiently captured and stored. Here we demonstrate that H(2) can be produced in a single process by capturing the salinity driven energy along with organic matter degradation using exoelectrogenic bacteria. Only five pairs of seawater and river water cells were sandwiched between an anode, containing exoelectrogenic bacteria, and a cathode, forming a microbial reverse-electrodialysis electrolysis cell. Exoelectrogens added an electrical potential from acetate oxidation and reduced the anode overpotential, while the reverse electrodialysis stack contributed 0.5-0.6 V at a salinity ratio (seawater:river water) of 50. The H(2) production rate increased from 0.8 to 1.6 m(3)-H(2)/m(3)-anolyte/day for seawater and river water flow rates ranging from 0.1 to 0.8 mL/ min. H(2) recovery, the ratio of electrons used for H(2) evolution to electrons released by substrate oxidation, ranged from 72% to 86%. Energy efficiencies, calculated from changes in salinities and the loss of organic matter, were 58% to 64%. By using a relatively small reverse electrodialysis stack (11 membranes), only ~1% of the produced energy was needed for pumping water. Although Pt was used on the cathode in these tests, additional tests with a nonprecious metal catalyst (MoS(2)) demonstrated H(2) production at a rate of 0.8 m(3)/m(3)/d and an energy efficiency of 51%. These results show that pure H(2) gas can efficiently be produced from virtually limitless supplies of seawater and river water, and biodegradable organic matter.
UR - http://hdl.handle.net/10754/598536
UR - http://www.pnas.org/cgi/doi/10.1073/pnas.1106335108
UR - http://www.scopus.com/inward/record.url?scp=80053630813&partnerID=8YFLogxK
U2 - 10.1073/pnas.1106335108
DO - 10.1073/pnas.1106335108
M3 - Article
C2 - 21930953
SN - 0027-8424
VL - 108
SP - 16176
EP - 16181
JO - Proceedings of the National Academy of Sciences
JF - Proceedings of the National Academy of Sciences
IS - 39
ER -