Wormlike core–shell nanoparticles formed by co-assembly of double hydrophilic block polyelectrolyte with oppositely charged fluorosurfactant
Wormlike core–shell nanoparticles formed by co-assembly of double hydrophilic block polyelectrolyte with oppositely charged fluorosurfactant
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双亲水嵌段聚电解质与带相反电荷的含氟表面活性剂共组装形成蠕虫状核壳纳米粒子
DOI:
10.1039/c2sm25588j
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发表时间:
2012
期刊:
影响因子:
3.4
通讯作者:
S. Pispas
中科院分区:
文献类型:
--
作者:
M. Štěpánek;Juraj Škvarla;Mariusz Uchman;K. Procházka;B. Angelov;L. Kováčik;V. Garamus;C. Mantzaridis;S. Pispas
Formation of polyelectrolyte–surfactant complexes (PE–S) between an anionic polyelectrolyte, poly(sodium 2-sulfamate-3-carboxylate isoprene)-block-poly(ethylene oxide) (PSCI-PEO) and a cationic fluorosurfactant, N-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl) pyridinium chloride (HFDPCl) was studied in alkaline aqueous solutions by static, dynamic and electrophoretic light scattering. The structure of the formed PE–S nanoparticles was investigated by SAXS, cryogenic transmission electron microscopy and atomic force microscopy. The results show that the tendency of the fluorosurfactant to form elongated threadlike micelles drives the PE–S co-assembly to a flexible core–shell cylindrical morphology with the core of the PE–S and the shell of the PEO blocks. Unlike other PE–S systems involving double hydrophilic polyelectrolytes, well-defined core–shell particles exist only in the narrow range of HFDPCl-to-PSCI unit stoichiometric ratios corresponding to zero ζ-potential of the aggregates.