Adsorption of Pluronic Surfactants in Alkylene Carbonates on Silica.
Masaki HanzawaHidekazu OohinataShin-Ichi KawanoMasaaki AkamatsuKenichi SakaiHideki SakaiPublished in: Langmuir : the ACS journal of surfaces and colloids (2018)
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.
Keyphrases
- atomic force microscopy
- single molecule
- high speed
- ionic liquid
- aqueous solution
- photodynamic therapy
- magnetic resonance imaging
- electronic health record
- metabolic syndrome
- magnetic resonance
- organic matter
- big data
- single cell
- adipose tissue
- machine learning
- glycemic control
- insulin resistance
- high resolution
- deep learning
- diffusion weighted imaging