Related Experiment Video
Updated: Jan 15, 2026

Synthesis of Biocompatible Liquid Crystal Elastomer Foams as Cell Scaffolds for 3D Spatial Cell Cultures
Published on: April 11, 2017
Design of oleofoams from citric acid esters of mono-/diglycerides
Carolina Ugarte-Pereyra1, Smaragda-Maria Argyri1, Romain Bordes2
1INRAE, University Lille, CNRS, INRAE, Centrale Lille, UMET, 59000 Lille, France.
Abstract:
Citric acid esters of mono- and diglycerides (CITREM E472c) are widely used as emulsifiers in the food industry. They result from the esterification of citric acid with mono- and diglycerides of fatty acids. CITREM was recently shown to produce stable aqueous foams but its potential in oil foam production remains unexplored. Due to its unique chemical structure, featuring free hydroxyl groups, along with its solubility in vegetable oils, CITREM is a highly promising candidate for this application. This study aimed to investigate the possibility of using CITREM as a surfactant to produce vegetable oil foams. We first determined the solubility of CITREM in sunflower oil to identify the solubility limit and the crystal formation temperature. We determined the critical aggregation concentration (CAC) of CITREM through Small Angle X-ray scattering (SAXS). The foamability was examined above the melting point at different surfactant concentrations. The impact of crystal formation on the foam stability was also examined at various storage temperatures. To determine the mechanisms leading to foam formation and stabilization, a multiscale approach was used by combining macroscopic observations of the foam, with optical microscopy and SAXS. We showed that oil foams were produced only above the CAC. We demonstrated that CITREM surfactants stabilize oil foams in the same manner as sucrose ester and sorbitan ester surfactants confirming that the key factor in forming vegetable oil foams with surfactants is the use of a lipophilic surfactant containing free hydroxyl groups, which can form hydrogen bonds with the triglycerides in the oil.
More Related Videos
07:01Preparation of Hollow Polystyrene Particles and Microcapsules by Radical Polymerization of Janus Droplets Consisting of Hydrocarbon and Fluorocarbon Oils
Published on: January 25, 2018
10:43Preparation, Purification, and Use of Fatty Acid-containing Liposomes
Published on: February 9, 2018
Related Concept Videos
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
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...
β-Dicarbonyl Compounds via Crossed Claisen Condensations