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No description available.

No description available.

No description available.

The research topic of liquid drop interaction with solid surfaces is being actively pursued to gain in-depth understanding of several practical cases such as the impingement of fuel spray droplets on surfaces like combustion chamber walls and piston top of an I.C. engine, heat transfer via spray impingement, ink-jet printing, etc. In most of the cases, the physical and flow properties of the liquid drop/spray may be fixed whereas it may be possible to tune the physical and chemical properties of the solid surface thereby enabling to control the interaction process. The present work belongs to the study of liquid drop-solid surface interaction process with special focus on the physical characteristics of solid surface. The thesis reports an experimental study of the dynamics of millimetric water drops impacted onto the junction of dual-textured substrates made of stainless steel. The dual-textured substrates consisted of hydrophobic (textured) and hydrophilic (smooth) portions. The entire textured portion comprised of parallel groove-like structures separated by solid posts/pillars. Two dual-textured substrates, which differ only in the geometry of their textured portions, were employed. Surface topography features of the dual-textured substrates were characterized using scanning electron microscopy (SEM) and optical surface profilometer. The wetting behavior of the textured and smooth portions of the substrates, quantified in terms of the equilibrium, advancing, and receding contact angles adopted by a water drop on the surface portions, was characterized experimentally through the methods of sessile drop formation, captive needle volume addition, and drop evaporation under ambient conditions. Free-falling water drops were impacted from a height onto the junction between the hydrophobic (textured) and hydrophilic (smooth) portions of the dual-textured substrates. A set of twelve different impact experiments were conducted on each of the target substrates with drop impact velocity (Uo) ranging from 0.37 to 1.50 m/sec. The dynamics of drop impact were captured using a high speed camera with frame rate ranging from 3000 to 10000 frames per second. From the captured frames, the temporal variations of the impacting drop parameters were measured using a MATLAB-assisted program. A systematic analysis of experimental data revealed the existence of four distinct regimes of drop dynamics on the dual-textured substrate: (a) early inertia driven drop spreading, (b) primary drop receding, (c) secondary spreading on the hydrophilic portion, and (d) final equilibrium regimes. It is shown that the drop impact dynamics during the early inertia driven impact regime remains unaffected by the dual-texture feature of the substrate. A larger retraction speed of impacting drop liquid observed on the hydrophobic portion of the substrate makes the drop liquid on the higher wettability/hydrophilic portion to advance further (secondary drop spreading). The net horizontal drop velocity towards the hydrophilic portion of the dual-textured substrate decreases with increasing drop impact velocity. The available experimental results suggest that the movement of bulk drop liquid away from the impact point during drop impact on the dual-textured substrate is larger for the impact of low inertia drops. A semi-empirical model, based on the balance of the wettability gradient, contact angle hysteresis, and viscous forces acting on impacted drop liquid on the substrate, is formulated to predict the movement of bulk drop liquid away from the impact point (ξ). A satisfactory comparison between the model predictions and the experimental measurements is reported for the variation of ξ with Uo.

Boiling is used in a wide variety of industries, including electronics cooling, distillation, and power generation. Fundamental studies on the boiling process are needed for effective implementation. Key performance characteristics of boiling are the heat transfer coefficient, which determines the amount of heat flux that can be dissipated for a given superheat, and critical heat flux(CHF), the failure point that occurs when vapor blankets the surface. The wettability of a surface is one of the key parameters that affects boiling behavior. Wetting surfaces(e.g., hydrophilic surfaces), typically characterized by a static contact angle below 90°,have better critical heat flux due to effective rewetting, but compromised heat transfer coefficients due to increased waiting times between nucleation of each bubble. Meanwhile, nonwetting surfaces (e.g., hydrophobic surfaces), characterized by static contact angles greater than 90°, have better heat transfer coefficients due to improved nucleation characteristic, but reach critical heat flux early due to surface dry out. However, recent studies have shown that the static contact angle alone offers and incomplete, and sometimes inaccurate, description of this behavior, which is instead governed entirely by the dynamic wettability. Specifically, the receding contact angle impacts the size and contact area of bubbles forming on a surface during boiling, while the advancing contact angle determines how the bubble departs. With this more complete set of wettability descriptors, three characteristic wetting regimes define the boiling behavior: hygrophilic surfaces having advancing and receding contact angles both under 90°; hygrophobic surfaces having both these dynamic contact angles over 90°;and ambiphilic surfaces having a receding contact angle less than 90°, but an advancing contact angle greater than 90°.The goal of this thesis is to experimentally characterize and compare the behavior of boiling surfaces in each of these regimes, observe the contact line behavior, and explain the mechanisms for their differences in performance.

Switching of surface composition and morphology of binary polymer brushes in response to changes in solvent selectivity, heating above glass transition temperatures, and contact with a rubbery stamp was studied. The binary brushes: polystyrene/poly(2-vinyl pyridine) (PS/P2VP), poly(styrene-co-2,3,4,5,6-pentafluorostyrene)/poly(methyl (meth)acrylate) (PSF/P(M)MA), and PS/PMMA were synthesized via two-step surface-initiated radical polymerization. Wetting experiments show that switching of brushes? surface composition upon exposure to solvents of various thermodynamic quality occurs faster than in 6 s. It takes longer time (5-10 min), if rate of solvent diffusion into the brush film is low. Discontinuous switching of surface composition of binary brushes is found upon exposure to binary solvents with gradually changed selectivity. X-ray Photoelectron Spectroscopy (XPS) shows quantitatively that the top brush layer (1) is dominated by respective favourite polymers after exposure to solvents of opposite selectivity and (2) comprises both brush constituents in almost symmetric ratio after exposure to non-selective solvents. Morphologies of binary brushes obtained after exposure to the solvents were studied with Atomic Force Microscopy (AFM). Local top layer composition was sensed with X-ray Photoemission Electron Microscopy (XPEEM). The morphologies are relevant to the particular solvents, reproducible, and independent on previous solvents. Phase segregation beneath the brush top layers was visualized with plasma etching. Qualitative agreement of the experimentally observed morphologies and predicted with self-consistent field theory is found. Enrichment of a binary brush top layer with the polymer providing lower surface energy takes place after annealing. Perpendicular segregation of binary brush constituents was sensed with XPEEM on perpendicular walls of imprinted elevations after wet microcontact printing.