Controlling the impact of drops onto solid surfaces is important for a wide variey of coating and deposition processes--for example, the treatment of plants with herbicides and pesticides requires precise targeting in order to meet stringent toxicological regulations. However, the outer wax-like layer of the leaves is a non-wetting substrate that causes sprayed droplets to rebound; often less than 50% of the initial spray is retained by the plant. Although the impact and subsequent retraction of non-wetting aqueous drops on a hydrophobic surface have been the subjects of extensive experimental and theoretical work, non-newtonian rheological effects have not been considered in any detail. Here we report that, by adding very small amounts of a flexible polymer to the aqueous phase, we can inhibit droplet rebound on a hydrophobic surface and markedly improve deposition without significantly altering the shear viscosity of the solutions. Our results can be understood by taking into account the non-newtonian elongational viscosity, which provides a large resistance to drop retraction after impact, thereby suppressing droplet rebound.

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The alkytrimethylammonium bromide surfactant series, CnTAB, n ) 10, 12, 14, 16, is used to perform a systematic study of the forces and stability of foam films produced from soluble cationic surfactants. Both surface tension and disjoining pressure isotherms are measured for each surfactant. This information is then combined with neutron reflectivity and dynamic surface tension results found in the literature to provide an understanding of how the surfactant chain length can effect the forces and stability in thinliquid films. For stable films, we find good quantitative agreement between the interaction forces measured in foam films and those reported from surface force studies on similar systems. We also find that the surfactant's hydrocarbon chain length and packing can strongly influence film stability. For highly purified surfactants an abrupt increase in film stability is seen when extending the chain length from C 12TAB to C14TAB. When an uncharged cosurfactant is present, this stability transition takes place between C10TAB and C12TAB. Both transitions correlate well with changes in the monolayer's cohesive strength, and we outline how monolayer cohesion can play a stabilizing role by dampening both spatial and density fluctuations at the air-water interface.