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Adsorption of Pluronic Surfactants in Alkylene Carbonates on Silica.
Hanzawa, Masaki; Oohinata, Hidekazu; Kawano, Shin-Ichi; Akamatsu, Masaaki; Sakai, Kenichi; Sakai, Hideki.
Afiliación
  • Oohinata H; Nomura Micro Science Co., Ltd., 2-4-37 Okata , Atsugi , Kanagawa 243-0021 , Japan.
  • Kawano SI; Nomura Micro Science Co., Ltd., 2-4-37 Okata , Atsugi , Kanagawa 243-0021 , Japan.
Langmuir ; 34(47): 14180-14185, 2018 11 27.
Article en En | MEDLINE | ID: mdl-30404452
Adsorption of triblock Pluronic surfactants bearing poly(ethylene oxide) (PEO) chains of different lengths, L-62 (5 EO groups on each end), L-64 (13 EO groups on each end), and F-68 (79 EO groups on each end), on silica has been characterized using atomic force microscopy (AFM). The solvent used herein was a mixture of ethylene carbonate (EC) and propylene carbonate (PC). The three Pluronic surfactants were dissolved in the mixed solvent, with the PEO chain acting as a solvophilic group and the poly(propylene oxide) (PPO) chain acting as a solvophobic group. The approaching force curve measurements for the three Pluronics (at 10 mmol dm-3) revealed repulsive forces from an apparent separation of 20-30 nm. The most solvophilic Pluronic surfactant with the longest PEO chain (F-68) showed continuously increasing repulsive interaction with decreasing separation. The Milner-Witten-Cates (MWC) theory described the repulsive force curve data of F-68, suggesting that F-68 forms a polymer brush on the silica surface. The retracting force curve measurements detected stretching forces for the three Pluronic systems. These stretching forces were observed more frequently for the L-62 system than for the F-68 system, but the pull-off distance was shorter for L-62 than for F-68.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2018 Tipo del documento: Article