Related Experiment Video
Updated: Jun 11, 2025

Fractionation of Lignocellulosic Biomass using the OrganoCat Process
Published on: June 5, 2021
Conversion of Cellobiose to Formic Acid as a Biomass-Derived Renewable Hydrogen Source Using Solid Base Catalysts.
Ikuto Yoshiki1, Atsushi Takagaki2, Jun Tae Song1,3
1Department of Applied Chemistry, Faculty of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, 819-0395, Japan.
Formic acid production from cellobiose was improved using combined solid acid and base catalysts. This method achieved a 33% yield under mild conditions, avoiding harmful byproducts.
Area of Science:
- Green Chemistry
- Catalysis
- Biomass Conversion
Background:
- Formic acid is a key hydrogen carrier derived from biomass.
- Oxidative decomposition of sugars offers a route to biomass-derived formic acid.
- Cellobiose, a glucose-based disaccharide, is a potential feedstock.
Purpose of the Study:
- To explore formic acid production from cellobiose using heterogeneous catalysts.
- To investigate mild reaction conditions for efficient formic acid synthesis.
- To overcome challenges in selective formic acid production from cellobiose.
Main Methods:
- Utilized alkaline earth metal oxide solid base catalysts (CaO, MgO) with hydrogen peroxide.
- Employed a combination of solid acid and solid base catalysts.
- Conducted reactions at mild temperatures (343 K).
Main Results:
- CaO catalyst yielded 14% formic acid but formed harmful CaO2.
- MgO catalyst produced formic acid without peroxide formation.
- Combined acid-base catalysis achieved a 33% formic acid yield due to efficient cellobiose hydrolysis and selective glucose decomposition.
Conclusions:
- Combined solid acid and base catalysis significantly enhances formic acid yield from cellobiose.
- Mild reaction conditions and heterogeneous catalysts offer a sustainable route for formic acid production.
- This approach avoids problematic metal peroxide byproducts, presenting a greener alternative.
More Related Videos
08:09A Novel Method for the Pentosan Analysis Present in Jute Biomass and Its Conversion into Sugar Monomers Using Acidic Ionic Liquid
Published on: June 1, 2018
16:33Methods for Facilitating Microbial Growth on Pulp Mill Waste Streams and Characterization of the Biodegradation Potential of Cultured Microbes
Published on: December 12, 2013
Related Concept Videos
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
The carbonyl center is...
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Fates of Pyruvate
In aerobic organisms, pyruvate is metabolized via the citric acid cycle to produce reduced coenzymes NADH and FADH2. These coenzymes are then oxidized in the electron transport chain to produce ATP and, in the process, regenerate the NAD+ and FAD. As seen in some cell types and organisms, fermentation...