Studies on Bioethanol Production From Selected Agro-Residues

Loading...
Thumbnail Image
Date
2011
Journal Title
Journal ISSN
Volume Title
Publisher
UAS Dharwad
Abstract
The present study was conducted on bioethanol production from selected agroresidues with the objectives of achieving higher recovery of fermentable sugars through delignification and saccharification followed by fermentation of the derived sugars to bioethanol. Five agro-residues namely sugarcane bagasse, sugarcane tops, sugarcane trash, corn husk and corn stover of particle sizes 0.5, 1.0 and 10.0 mm were delignified by various pre-treatment methods such as alkali, autohydrolysis and lignolytic fungi. The treatment combination of 3.0% NaOH with 1210C temperature for one h on particle size 0.5 mm resulted in the highest recovery of cellulose and hemicelluloses in sugarcane bagasse (0.813 g/g), sugarcane tops (0.786 g/g), sugarcane trash (0.806 g/g), corn husk (0.806 g/g) and corn stover (0.806 g/g). The delignified substrates were further saccharified using cellulolytic fungi and their crude enzymes and commercial cellulase enzymes. Among these, the commercial cellulase enzyme with 15 U/g along with b-glucosidase (10 U/g ) and Xylanase (5 U/g) enzymes at 5% substrate produced significantly highest reducing sugars with per cent saccharification in sugarcane bagasse (93.17%), sugarcane tops (90.33%), sugarcane trash (84.61%), corn husk (80.61%) and in corn stover (80.80%) in 12 h of incubation period. The pre-treated substrates were fermented to bioethanol by using six microorganisms. The combined inoculation of Saccharomyces cerevisiae and Candida shihatae on pre-treated substrates resulted in the highest ethanol yield in all the substrates, sugarcane bagasse (278.40 mg/g) followed by sugarcane tops (262.75 mg/g), sugarcane trash (241.42 mg/g), corn stover (239.82 mg/g) and corn husk (232.36 mg/g). The scaled up study on bioethanol production with sugarcane bagasse under optimized conditions produced 223 g bioethanol from one kg pre-treated substrate. Thus, it can be concluded that the substrates need to be alkali pretreated followed by treatment with commercial enzymes and further conversion to ethanol. The combined inoculation of the yeast cultures yields maximum ethanol.
Description
Keywords
Citation
Collections