Mixed micelles of poly(styrene-b-3-(methacryloylamino)propyltrimethylammonium chloride-b-ethylene oxide) and anionic amphiphiles in aqueous solutions

Author:

Liu Jingjing12,Yoneda Airi12,Liu Dian12,Yokoyama Yuuichi12,Yusa Shin-ichi12,Nakashima Kenichi12

Affiliation:

1. Department of Chemistry, Faculty of Science and Engineering, Saga University, 1 Honjo-machi, Saga 840-8502, Japan.

2. Department of Materials Science and Chemistry, University of Hyogo, 2167 Shosha, Himeji 671-2280, Japan.

Abstract

The micelles of poly(styrene-b-3-(methacryloylamino)propyltrimethylammonium chloride-b-ethylene oxide) (PS-b-PMAPTAC-b-PEO) have been successfully prepared in aqueous solutions. The micelles have a PS core, cationic PMAPTAC shell, and PEO corona. Due to the short PS chain (degree of polymerization = 8), the formation of micelles is difficult at a low concentration, and the micelles are detected only at concentrations higher than 1 g L–1. The addition of anionic amphiphiles, such as sodium dodecyl sulfate (SDS) and poly(methacrylic acid) (PMAA), induces the formation of mixed micelles at a low concentration level of the polymer (~0.005 g L–1). This can be ascribed to insolubilization of the cationic PMAPTAC block due to charge neutralization by the anionic amphiphiles. The binding of SDS or PMAA to the PMAPTAC block is confirmed by zeta-potential measurements. The mixed micelles are characterized by dynamic light scattering (DLS), scanning electron microscopy (SEM), and fluorescence measurements. Based on DLS measurements, it is revealed that the hydrodynamic diameter of the mixed micelles falls in the range of 120–130 nm. SEM measurements provided clear pictures of mixed micelles with a spherical morphology. The kinetics of exchange of organic dyes between the micelle particles was investigated by fluorescence techniques. The result indicates that the exchange of the dyes between the micelle particles takes places within a time scale of seconds.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

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