Related Experiment Video
Updated: Dec 6, 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
Preparation of kapa carrageenan-based acidic heterogeneous catalyst for conversion of sugars to high-value added
Mahsa Rezaie1, Mohammad Dinari2, Alireza Najafi Chermahini2
1Chemistry Group, Pardis College, Isfahan University of Technology, Isfahan 84156-83111, Iran.
Abstract:
A novel composite based on kappa-Carrageenan (κC) was prepared using N,N-methylene bisacrylamide (MBA) as the crosslinking agent. 5-Hydroxymethylfurfural (5-HMF) was produced by catalytic dehydration of fructose and glucose with MBA grafted κC (κC-g-MBA) as the solid acid catalyst due to sulfonic acid groups in biopolymer skeletons. Various reaction parameters such as optimization of the quantity of the catalyst, temperature, reaction time, and solvent were performed. It was established that for fructose dehydration, the best reaction conditions were the 160 °C as the optimized reaction temperature and 1 h reaction time, respectively. Under these conditions, the HMF yield and fructose conversion were 94.2% and 95.5%, respectively. Furthermore, 160 °C and 2 h were the best reaction temperature and reaction time for glucose dehydration, respectively. Under similar conditions, the HMF yield and glucose conversion are 47% and 93%, respectively. The catalyst was readily prepared from inexpensive materials with considerable reusability and reactivity.
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...
Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents
Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives
Carboxylic acid derivatives like acid chlorides and esters are more easily reducible than the corresponding acids. The derivatives reduce in the presence of mild reducing agents to give aldehydes. Aldehydes can also be prepared by Rosenmund reduction, that is, the reduction of...
Preparation of Carboxylic Acids: Overview
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Preparation of Acid Anhydrides
The carboxylate ion acts as a nucleophile that attacks the carbonyl carbon of the acid chloride to form a tetrahedral intermediate. Subsequently, the re-formation of the carbonyl group with the loss of the chloride ion as a leaving group leads to the formation of an acid...

