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Measurement of forces between two mica surfaces in aqueous electrolyte solutions in the range 0–100 nm
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The main results and conclusions of experimental measurements of the forces between molecularly smooth mica surfaces in aqueous electrolyte solutions are as follows: as mentioned in this paper, and they are based on the following assumptions:Abstract:
The main results and conclusions of experimental measurements of the forces between molecularly smooth mica surfaces in aqueous electrolyte solutions are as follows:read more
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Liquid structuring at solid interfaces as probed by direct force measurements: The transition from simple to complex liquids and polymer fluids
TL;DR: In this paper, the minimum segment number when a flexible chain molecule begins to interact like a polymer was established, and the transition from simple liquid-like behavior (as occurs with short-chained alkanes) to that characteristic of long-chain polymers was investigated.
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Intermolecular Forces between a Protein and a Hydrophilic Modified Polysulfone Film with Relevance to Filtration.
TL;DR: Correlations between intermolecular forces and ultrafiltration measurements for a thin polysulfone film and membranes modified for increased hydrophilicity by graft polymerization of 2-hydroxyethyl methacrylate and a model protein suggest that altering either the chemistry of the polymer surface or the solution conditions should lead to a minimization of protein adhesion and hence fouling for a specific protein/polymer combination.
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Forces between bilayers of cetyltrimethylammonium bromide in micellar solutions
TL;DR: The apparent agreement of bilayer and micellar ion binding parameters raises an important challenge for theories of double-layer interactions.
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Adhesion mechanism in a DOPA-deficient foot protein from green mussels
TL;DR: The strong adhesion mechanism induced by cation-π interactions and conformational changes in pvfp-1 provides new insights for the development of biomimetic underwater adhesives.
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Fluidity of water confined down to subnanometer films.
TL;DR: No shear stress can be sustained by water down to films of thickness D = D0 = 0.0 +/- 0.3 nm, which contrasts sharply with the case of confined nonassociating liquids, whose effective viscosity increases by many orders of magnitude at film thicknesses lower than about five to eight monolayers.