Surface Activity of Hydrophobized Modified Starch Hydrolysates in Mixed Systems
[ 1 ] Instytut Chemii i Elektrochemii Technicznej, Wydział Technologii Chemicznej, Politechnika Poznańska | [ 2 ] Instytut Technologii i Inżynierii Chemicznej, Wydział Technologii Chemicznej, Politechnika Poznańska | [ P ] employee
2024
scientific article
english
- chemically modified starch
- dynamic surface tension
- emulsion stability
- polysaccharide emulsifiers
- surface activity
- surface mole fraction
- synergistic effect
EN The manuscript presents research focusing on the adsorption and emulsion properties of starch hydrolysates modified through acetylation, oxidation, and cross-linking. The techniques used in this study included measurements of equilibrium surface tension (du Noüy ring) dynamic surface tension (drop shape analysis), and the preparation and evaluation of emulsion stability (TURBISCAN). The surface activity of the acetylated starch hydrolysates is affected by the degree of acetylation. The acetylated starch 0.02Ac-H exhibited higher surface activity than the more highly substituted derivative 0.1Ac-H. Furthermore, it was shown that the surface activity of the components increased as the acetylated oxidized starch underwent hydrolysis. The fractions collected after 180 min using a membrane with a low separation capability (8 kDa) revealed the highest capacity for reducing surface tension. In binary systems consisting of starch derivatives and surfactants, synergistic effects in reducing surface tension were particularly noticeable in systems containing ionic surfactants. The addition of a cationic surfactant to the modified starch hydrolysate solution (1:6 mol/mol) resulted in a significantly more efficient saturation of the air/water interface. This study demonstrated that emulsions stabilized with modified starch hydrolysates remained stable over time, even when these hydrolysates constituted up to 60% of the emulsifier mixture.
12.11.2024
5526-1 - 5526-20
Article number: 5526
CC BY (attribution alone)
open journal
final published version
at the time of publication
public
140
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