Outdoor cultivation of Chlamydomonas reinhardtii for photobiological hydrogen production

• Published in: Journal of applied phycology 2012-06, Vol.24 (3), p.319-327
• Main Authors: Geier, Stephanie C, Huyer, Sabine, Praebst, Konstantin, Husmann, Moritz, Walter, Christian, Buchholz, Rainer
• Format: Article
• Language: English
• Subjects: anaerobic conditions; biomass; Biomedical and Life Sciences; bioreactors; biosynthesis; carbon dioxide; Chlamydomonas reinhardtii; design for environment; Ecology; ferredoxin hydrogenase; Freshwater & Marine Ecology; hydrogen; hydrogen production; Life Sciences; light intensity; oxygen; photosynthesis; Plant Physiology; Plant Sciences; solar radiation; summer
• ISSN: 0921-8971; 1573-5176
• DOI: 10.1007/s10811-011-9729-5

Photobiological hydrogen production by the unicellular green alga Chlamydomonas reinhardtii has been studied under laboratory conditions to a vast extend but has not been investigated under outdoor conditions yet. Because the hydrogen-producing hydrogenase is very sensitive to oxygen, the production must be performed in a two-stage process: generation of the required algal biomass under oxygenic photosynthesis, followed by hydrogen biosynthesis under anaerobic conditions. In order to design a sustainable process, cultivation and subsequent hydrogen production under cost-free sunlight was investigated in this work for the first time. First, cells were grown in closed photobioreactors under simulated outdoor conditions according to the light intensities of an idealized summer day (up to 2,000 μmol photons m−2 s−1) in order to achieve results independent of varying, and therefore not reproducible, weather conditions. The following outdoor experiments showed comparable growth characteristics and similar cell densities. However, the use of cells grown under outdoor, simulated outdoor, or high light conditions generally resulted in significantly lower hydrogen yields compared to the use of cells cultivated under low and continuous irradiance. In order to lower cultivation costs during the growth phase, the use of 10% CO2 corresponding to the CO2 content of flue gas was investigated. By supplying additional CO2 during growth under the light profile corresponding to an idealized summer day, no significant increase of cell densities could be achieved, but the subsequent hydrogen production increased compared to hydrogen production of cells grown under atmospheric CO2.