1996
DOI: 10.1016/0927-7757(96)03593-5
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The relationship between surfactant structure and limiting values of surface tension, in aqueous gelatin solution, with particular regard to multilayer coating

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Cited by 69 publications
(96 citation statements)
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“…2, the MWCNTs/NR-latex containing 24.00 mM TC14 exhibited the highest electrical conductivity. A comparison of the conductivity results for the series of SDS (mono-chain), AOT14 (di-chain) and TC14 (tri-chain) revealed a clear trend of increasing electrical conductivity with increasing number of tails, as reported previously [22,35,36]. However, a discrepancy in conductivity can be seen for TC14 systems with below cmc (21.63 mM) due to dynamic equilibrium behaviour of surfactant at MWCNT interface.…”
Section: Electrical Conductivity Measurementsmentioning
confidence: 75%
“…2, the MWCNTs/NR-latex containing 24.00 mM TC14 exhibited the highest electrical conductivity. A comparison of the conductivity results for the series of SDS (mono-chain), AOT14 (di-chain) and TC14 (tri-chain) revealed a clear trend of increasing electrical conductivity with increasing number of tails, as reported previously [22,35,36]. However, a discrepancy in conductivity can be seen for TC14 systems with below cmc (21.63 mM) due to dynamic equilibrium behaviour of surfactant at MWCNT interface.…”
Section: Electrical Conductivity Measurementsmentioning
confidence: 75%
“…25 This remarkable reduction in surface tension is believed to be a direct consequence of increasing the CH3:CH2 ratio per headgroup (increase the branching using "hedgehog" tail structures), since the CH3-has a lower γcmc than -CH2-based on the following trend of CF3-< -CF2-< CH3-< -CH2-. 52 …”
Section: Resultsmentioning
confidence: 99%
“…In water, however, the hydrophobic nature of graphene leads to the agglomeration of graphene sheets into graphitic layered structures or agglomerates, thus spontaneous wetting by water is theoretically impossible. It has long been established in colloid science that to achieve a thermodynamically stable dispersion of one phase in another requires the lowering the interfacial energy between two immiscible phases, using surfactants that either strongly bind to the target compound or are solvated by the continuous phase [87][88][89]. However, very little is known as to whether graphene dispersions can be thermodynamically stable [90].…”
Section: Graphene-compatible Surfactantsmentioning
confidence: 99%