Related Experiment Video
Updated: Sep 11, 2025

Author Spotlight: Optimizing Hollow-Fiber Membranes for Continuous Liquid-Liquid Extraction of Medium-Chain Fatty Acids
Published on: August 9, 2024
"On-Water" Interfacial Acidification Enhances Direct Ammonolysis of Triglycerides
Jie Gao1, Kang Wang2, Yunjiao Gu1,3
1Eco-Efficient Products and Processes Laboratory (E2P2L), UMI 3464 CNRS-Solvay, Shanghai, 201108, China.
Abstract:
Direct ammonolysis of triglycerides with liquid ammonia is a well-established technology for the industrial manufacture of aliphatic amides typically requiring a large excess of ammonia. In this study, using glyceryl trilaurate (GTL) as a model triglyceride, we demonstrate that the rate of lauramide formation can be enhanced sevenfold at 150 °C and low ammonia excess (47:1 mol/mol ammonia/GTL) when the reaction is carried out in GTL-in-water(acetonitrile) (50:50 v/v) emulsions stabilized by surface-active Aquivion perfluorosulfonic superacid (PFSA) particles, compared to a non-emulsified system. Moreover, the lauramide yield after 5 h is nine times higher than that achieved with conventional ammonolysis in liquid ammonia at higher ammonia excess (148:1 mol/mol ammonia/GTL). This significant increase in activity is attributed to the "on-water" selective acidification at the microstructured oil-water interface facilitated by adsorbed Aquivion PFSA particles, in combination with enhanced ammonia solubilization and selective glycerol extraction by the water(acetonitrile) phase.
Related Concept Videos
Amides to Carboxylic Acids: Hydrolysis
Acid-catalyzed hydrolysis:
Hydrolysis of amides under acidic conditions yields carboxylic acids. Since the reaction occurs slowly, hydrolysis requires the conditions of heat.
The mechanism begins with the protonation of the carbonyl oxygen by the acid catalyst. The protonation makes the amide carbonyl carbon more...
Acid Halides to Amides: Aminolysis
In the first step of the aminolysis mechanism, the amine attacks the carbonyl carbon of the acyl chloride to form a tetrahedral intermediate. In the second step, the carbonyl group is re-formed with the elimination of a chloride...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
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 Mechanism
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...

