Related Experiment Video
Updated: May 12, 2026

Preparation of Expanded Chitin Foams and their Use in the Removal of Aqueous Copper
Published on: February 27, 2021
Homogeneous synthesis of chitin-based acrylate superabsorbents in NaOH/urea solution
Tingguo Liu1, Liwu Qian, Bin Li
1Provincial-Level Experimental and Teaching Demonstration Center of Chemical Materials & Engineering, Chizhou University, Anhui Chizhou 247100, People's Republic of China. liutg137@hotmail.com
Abstract:
A modified freezing-thawing cyclic (FTC) process was applied to dissolve the chitin in NaOH/urea solution. A transparent homogeneous solution was obtained. It was utilized directly for preparing the superabsorbent polymers (SAPs) by grafting copolymerization under static solution conditions without nitrogen protection. The acrylic acid was used conveniently without prior neutralization. The final products existed as hydrogels without excess reagent emissions. The adsorption capacity and yield of SAP that was prepared in the optimum conditions was 2833 g/g and 81.65%, respectively, higher than one-time FTC program prepared with 2527 g/g and 15.44%. Furthermore, it formed a uniform and transparent gel without any residual chitin particles. The regenerated chitin and SAPs were characterized by SEM, FTIR, XRD, and TG. The samples prepared by the new method presented a more amorphous state with good thermal stability, suggesting that this convenient preparation method for a potential industrial application's pathway.
More Related Videos
Related Concept Videos
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...
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Preparation of Amides
The DCC-promoted synthesis of amides begins with the protonation of DCC by carboxylic acid. The protonation makes it a better acceptor. Next, the addition of carboxylate to the protonated carbodiimide gives a reactive acylating agent.
Subsequently, the amine acts as a nucleophile that attacks the acylating agent to form a tetrahedral intermediate. In the...
Anionic Chain-Growth Polymerization: Overview

