Related Experiment Video
Updated: Dec 20, 2025
Techniques for the Evolution of Robust Pentose-fermenting Yeast for Bioconversion of Lignocellulose to Ethanol
Published on: October 24, 2016
A new biorefinery platform for producing (C2-5) bioalcohols through the biological/chemical hybridization process
Sungyup Jung1, Hana Kim2, Yiu Fai Tsang3
1Department of Environment and Energy, Sejong University, Seoul 05006, Republic of Korea.
Abstract:
This review presents an emerging biorefinery platform for C2-5 bioalcohol production through chemical synthesis using the organic waste materials. Bioalcohols are the most commercialized carbon-neutral transportation fuels, compatible with existing an internal combustion (IC) engine. However, current bioalcohol fermentation processes have made from sugar-rich edible crops. Also, carbon loss from the fermentation process is substantial. To minimize carbon loss, volatile fatty acids (VFAs) can be utilized as a raw material for bioalcohol production. Thus, a two-step chemical upgrading of VFAs into C2-5 alcohols is summarized in comparison with current challenges of biological fermentation processes for bioalcohol production. This review also provides the prospect of the hybrid biological/chemical process, presenting the technical advantages of the system. Finally, economic viability of hybridized process for bioalcohol production is compared with the current biological process.
More Related Videos
10:10Genetic Engineering of an Unconventional Yeast for Renewable Biofuel and Biochemical Production
Published on: September 20, 2016
11:44Qualitative Characterization of the Aqueous Fraction from Hydrothermal Liquefaction of Algae Using 2D Gas Chromatography with Time-of-flight Mass Spectrometry
Published on: March 6, 2016
Related Concept Videos
02:15Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
01:38Preparation of Alcohols via Substitution Reactions
Alcohols can be synthesized from alkyl halides via nucleophilic substitution reactions. The highly polar carbon-halogen bond in the substrate makes halide a good leaving group. The hydroxide ion or water can act as a nucleophile to take the place of halide and form an alcohol. The substitution reactions occur via two different reaction pathways, SN1 or SN2, depending on the nature of carbon attached to the halide.
Primary alcohols are synthesized from primary alkyl halides, and the...
02:23Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
01:27Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview
00:46Bioremediation
03:08Hydroboration-Oxidation of Alkenes