Commercialization of the Conversion of Bagasse to Ethanol. Summary quarterly report for the period January-September 1999

BC International Corp., Hingham, MA (United States)

关键词: Heat Recovery;    Biosynthesis;    Escherichia Coli;    Commercialization;    Stillage;   

DOI  :  10.2172/755492
RP-ID  :  DOE/GO/10224-Q
RP-ID  :  FC36-97GO10224
RP-ID  :  755492

美国|英语

来源: UNT Digital Library

【 摘 要 】

These studies were intended to further refine sugar yield parameters which effect sugar yield such as feedstock particle size, debris, acid soak time, temperature, dewatering, and pretreatment conditions (such as temperature, reaction time, percentage solids concentration, acid concentration), liquid-solids separation, and detoxification parameters (such as time temperature and mixing of detoxification ingredients). Validate and refine parameters, which affect ethanol yield such as detoxification conditions mentioned above, and to fermenter conditions such as temperature, pH adjustment, aeration, nutrients, and charging sequence. Materials of construction will be evaluated also. Evaluate stillage to determine clarification process and suitability for recycle; evaluate lignocellulosic cake for thermal energy recovery to produce heat and electricity for the process; and Support Studies at UF - Toxin Amelioration and Fermentation; TVA work will provide pre-hydroylsates for the evaluation of BCI proprietary methods of toxin amelioration. Pre-hydrolysates from batch studies will allow the determination of the range of allowable hydrolyze conditions that can be used to produce a fermentable sugar stream. This information is essential to guide selection of process parameters for refinement and validation in the continuous pretreatment reactor, and for overall process design. Additional work will be conducted at UFRFI to develop improved strains that are resistant to inhibitors. The authors are quite optimistic about the long-term prospects for this advancement having recently developed strains with a 25%--50% increase in ethanol production. The biocatalyst platform selected originally, genetically engineered Escherichia coli B, has proven to be quite robust and adaptable.