Competitive adsorption of amylopectin and amylose on cationic nanoparticles: a study on the aggregation mechanism
Artikel i vetenskaplig tidskrift, 2016

In this study we investigate the interactions between cationic nanoparticles and anionic starch, where the starch was composed of 20 wt% of amylose, a linear polymer, and 80 wt% of amylopectin, a branched polymer. The mechanism of aggregation was investigated by scattering techniques. It was found that the cationic particles formed large aggregates with the starch as a result of selective adsorption of the amylopectin. Amylose did not participate significantly in the aggregate formation even when the charge ratio of starch to particles was <1. For starch to particle ratio 41 stabilization was recovered mostly due to the large hindrance brought about by the highly branched amylopectin. This results in a shift of the stabilization mechanism from electrostatic to electrosteric. The internal structure of the aggregates was composed of primary particles with starch coils adsorbed on the surface. This information supports the proposed aggregation mechanism, which is based on adsorption of the negatively charged starch in patches on the positively charged nanoparticles causing attractive interaction between the particles.

behavior

suspensions

Materials Science

silica

polymers

latex-particles

dynamic light-scattering

physicochemical properties

adsorbed polyelectrolytes

Chemistry

starches

flocculation

Författare

Frida Iselau

SuMo Biomaterials

Chalmers, Kemi och kemiteknik

Tuan Phan Xuan

SuMo Biomaterials

Chalmers, Fysik, Kondenserade materiens fysik

Aleksandar Matic

Chalmers, Fysik, Kondenserade materiens fysik

M. Persson

Akzo Nobel Surface Chemistry AB

Krister Holmberg

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Teknisk ytkemi

Romain Bordes

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Teknisk ytkemi

Soft Matter

1744-683X (ISSN) 1744-6848 (eISSN)

Vol. 12 3388-3397

Ämneskategorier

Polymerkemi

Fysik

Materialkemi

Drivkrafter

Hållbar utveckling

Styrkeområden

Materialvetenskap

DOI

10.1039/c6sm00165c