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Alternative anodic reactions in water splitting. Final report

Technical Report ·
DOI:https://doi.org/10.2172/6067620· OSTI ID:6067620
An anodic depolarization path to hydrogen production through water electrolysis has been examined, using lignite, grass and household wastes. Iron was removed from lignite by extensive washing. The degree of dissolution of lignite in 5 M H/sub 2/So/sub 4/ at 100/sup 0/C is ca. 0.1 wt %. Washed lignite dissolves less than unwashed material. Cyclic voltammograms showed peaks arising from dissolved organics. Increase of temperature produced more peaks. In alkaline solution, peaks disappeared. Oxidation currents were three times greater if the lignite particles were in contact with the electrode compared with their absence from solution. Platinum anodes oxidized lignite better than PbO/sub 2/. Redox systems, added to the electrolyte, helped compound formation. Grass and household wastes gave similar results but lower oxidation currents. Compounds present in solution prior to electrolysis dissolve off the internal surfaces of lignite particles. Increased oxidation currents, caused when lignite particles came in contact with the anode, arose, not because of enhanced electrochemical reactions, but from enhanced lignite dissolution following erosion. The organic compounds eventually form CO/sub 2/; the presence of heavy oils lasts for 10 hr. Current densities up to 750 mA cm/sup -2/ at ca. 1 V should be obtainable. The hydrocarbons are formed via a Kolbe mechanism from carboxylic acids. Speculative economic considerations show that the final cost of hydrogen produced, using lignite as an anode depolarizer, is considerably cheaper than that from natural gas: $0.40 per GJ, or less, compared to $5 per GJ.
Research Organization:
Brookhaven National Lab., Upton, NY (USA)
DOE Contract Number:
AC02-76CH00016
OSTI ID:
6067620
Report Number(s):
BNL-35458; ON: DE85004159
Country of Publication:
United States
Language:
English