Related Experiment Video
Updated: Jun 12, 2025

A 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
Corncob waste derived carbon with sulfonic acid group: An efficient heterogeneous catalyst for production of ethyl
Dian Ratna Suminar1, Cinantya Zahrina Pribadi2, Qonita Rahmah Fitriana2
1Department of Chemistry, Faculty Mathematics and Natural Sciences, Universitas Padjadjaran, Sumedang, 45363, Indonesia.
Abstract:
Alkyl levulinate is a biomass-based chemical compound used as a fuel additive. This research aims to produce ethyl levulinate from levulinic acid and ethanol using esterification with the assistance of a heterogeneous sulfonated carbon catalyst. The carbon sulfonate catalyst is obtained from corncob waste that has undergone carbonization at 300 °C and sulfonation using sulfuric acid at a temperature of 150 °C for 8 h. The catalyst is used for esterification with predetermined operating variables using Box-Behnken Design (BBD) on the response surface methodology (RSM). The result shows significant variables for ethyl levulinate esterification are catalyst loading and esterification time. The FTIR analysis indicates the presence of S=O bonds in the sulfonated carbon catalyst. The XRD and SEM analysis shows that the sulfonated carbon catalyst is in amorphous and mesoporous form. Catalyst reusability demonstrates that the corncob-derived carbon sulfonate catalyst can be used up to 3 times. The optimum condition for esterification is 9 h of reaction, 10 % catalyst loading, and a molar ratio of levulinic acid to ethanol of 1:10, which has 83.15 % conversion. These results present the optimum parameter conditions for an efficient heterogeneous catalyst from corncob for producing ethyl levulinate.
Related Concept Videos
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
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...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives

