Energy futuresNew source of energy: urine

Published 7 November 2011

Urine is the most abundant waste on Earth; American chemists have combined refueling one’s car and relieving one’s bladder by creating a new catalyst that can extract hydrogen from urine

American chemists have combined refueling one’s car and relieving one’s bladder by creating a new catalyst that can extract hydrogen from urine.

Chemistry World reports that the catalyst could not only fuel the hydrogen-powered cars of the future, but could also help clean up municipal wastewater.
A Royal Society of Chemistry release reports that Gerardine Botte of Ohio University uses an electrolytic approach to produce hydrogen from urine — the most abundant waste on Earth — at a fraction of the cost of producing hydrogen from water.
Urine’s major constituent is urea, which incorporates four hydrogen atoms per molecule — importantly, less tightly bonded than the hydrogen atoms in water molecules.
Botte uses electrolysis to break the molecule apart, developing an inexpensive new nickel-based electrode to selectively and efficiently oxidise the urea. To break the molecule down, a voltage of 0.37V needs to be applied across the cell — much less than the 1.23V needed to split water.
Her work is described in the Royal Society of Chemistry journal Chemical Communications (see more details here).
“During the electrochemical process the urea gets adsorbed on to the nickel electrode surface, which passes the electrons needed to break up the molecule,” Botte told Chemistry World.
Botte believes the technology could be easily scaled-up to generate hydrogen while cleaning up the effluent from sewage plants. “We do not need to reinvent the wheel as there are already electrolysers being used in different applications.”
She believes the only the thing that would hamper the process would be the presence of a lot of salt.
— Read more in Loannis Ieropoulos et al., “Urine utilisation by Microbial Fuel Cells; energy fuel for the future,” Physical Chemistry Chemical Physics (19 October  2011)  (DOI: 10.1039/C1CP23213D)