• Aucun résultat trouvé

Surface properties of two closely related sugar esters : glucose octanoate and octyl glucuronate.

N/A
N/A
Protected

Academic year: 2021

Partager "Surface properties of two closely related sugar esters : glucose octanoate and octyl glucuronate."

Copied!
1
0
0

Texte intégral

(1)

Surface properties of two closely related sugar esters: glucose octanoate and octyl glucuronate

C. Blecker1, C. Deroanne1, B. Moreau2,3, G. Lognay3, M. Marlier3, M. Paquot4

Faculté Universitaire des Sciences Agronomiques de Gembloux 1

Unité de Technologie des Industries Agro-alimentaires 2

Unité de Bio-industries 3

Unité de Chimie Générale et organique 4

Unité de Chimie Biologique Industrielle Passage des Déportés, 2 – B5030 Gembloux

Abstract

The surface properties of two closely related sugar esters, glucose octanoate and octyl glucuronate, are compared. Adsorption kinetic, interfacial viscoelasticity, critical micellar concentration (CMC), excess concentration and molecule area are presented for both surfactants.

The results clearly indicate that the ester bond position influences the extent and rate of interfacial adsorption and has implication on the surfactant performance. Octyl glucuronate exhibits a faster rate of adsorption at the air-water interface and a lower critical micellar concentration. Glucose octanoate presents higher viscoelasticity and elasticity moduli. These various interfacial properties derive from difference in the structure and the hydrophobic/hydrophilic nature of both sugar esters.

Références

Documents relatifs

10.Fire of the Holy Spirit, cancel and completely destroy all the covenants that bring evil things around my spirit, soul, body and family in the Name of Jesus. 11.I cancel and

Swiss Centre for Antibiotic Resistance (ANRESIS) network: Institute for Laboratory Medicine, Cantonal Hospital Aarau; Central Laboratory, Microbiology Section, Cantonal

Molecular dimensions can be derived from the surface pressure- concentration isotherms.. The results indicate that the benzene rings lie flat at

Here we scrutinize whether the actual structure of phospholipid monolayers in stratified layers parallel with the air/water interface, both under air and when interacting

positionally ordered, lamellar phase whose planes contain substantial water filled defects, It has been suggested that the structural unit in all three phases is a disk shaped

Fluorescence microscopy which allows one to image a monolayer directly on water, X-ray reflectivity and surface scattering which yield both the normal structure and the

The lyotropic phase behaviour of Cj~EO~ [12] is rather similar to that of p-OG : both systems form fluid lamellar and type I cubic and hexagonal Hi phases, and the space group of

Whereas for submicellar solution, common non-ionic surfactants molecules usually undergo a diffu- sion limited adsorption, we showed that the adsorption of free surfactants from