Interfacial phenomena play a crucial role in multiphase flow systems, governing interactions between different phases. Surface tension, a key concept, represents the energy required to increase a liquid's surface area, influencing droplet formation, wetting behavior, and capillary effects.
This unit explores the physical principles behind interfacial phenomena, including surface tension causes and effects, wetting and contact angles, and capillarity. It also covers measurement techniques, experimental methods, and modeling approaches used to study and predict interfacial behavior in various applications.
Interfacial phenomena encompasses interactions and processes occurring at the boundary between two phases (liquid-liquid, gas-liquid, solid-liquid)
Surface tension (γ) represents the energy required to increase the surface area of a liquid by a unit amount
Measured in units of force per unit length (N/m) or energy per unit area (J/m²)
Capillarity describes the ability of a liquid to flow in narrow spaces without the assistance of external forces
Wetting refers to the ability of a liquid to maintain contact with a solid surface
Determined by the balance of adhesive and cohesive forces
Contact angle (θ) quantifies the wettability of a solid surface by a liquid
Measured as the angle formed between the liquid-solid interface and the liquid-vapor interface
Interfacial forces include surface tension, disjoining pressure, and capillary pressure
Play a crucial role in the behavior and stability of multiphase systems
Adsorption involves the accumulation of molecules or atoms at an interface
Can modify interfacial properties and affect system behavior
Physical Principles of Interfacial Phenomena
Interfacial phenomena arise from the imbalance of molecular forces at the interface between two phases
Molecules at the interface experience unequal attractive forces compared to those in the bulk phase
Leads to an excess energy at the interface, known as surface free energy
Minimization of surface free energy drives the system towards a state of minimum surface area
Surface tension originates from the cohesive forces among liquid molecules
Stronger cohesive forces result in higher surface tension values
Interfacial tension exists between two immiscible liquids or a liquid and a gas
Governs the shape and stability of droplets and bubbles
Laplace pressure (ΔP) describes the pressure difference across a curved interface
Given by the Young-Laplace equation: ΔP=γ(R11+R21), where R1 and R2 are the principal radii of curvature
Marangoni effect refers to the mass transfer along an interface due to surface tension gradients
Caused by temperature, concentration, or surfactant gradients
Surface Tension: Causes and Effects
Surface tension arises from the imbalance of molecular forces at the liquid-vapor interface
Cohesive forces between liquid molecules are responsible for surface tension
Stronger intermolecular forces (hydrogen bonding, dipole-dipole interactions) lead to higher surface tension
Surface tension minimizes the surface area of a liquid to achieve a state of lowest energy
Causes liquids to form spherical droplets or menisci in capillaries
Factors affecting surface tension include temperature, pressure, and the presence of surfactants
Increasing temperature reduces surface tension by weakening intermolecular forces
Surfactants lower surface tension by adsorbing at the interface and reducing the imbalance of forces
Surface tension influences the formation and stability of emulsions, foams, and thin films
Capillary rise or depression in narrow tubes is a consequence of surface tension
Height of rise or depth of depression depends on the liquid's surface tension and the tube's radius
Marangoni convection occurs due to surface tension gradients
Drives the movement of liquids from regions of low surface tension to high surface tension
Wetting and Contact Angles
Wetting refers to the ability of a liquid to spread on a solid surface
Contact angle (θ) quantifies the wettability of a solid surface by a liquid
Measured as the angle between the liquid-solid interface and the liquid-vapor interface at the three-phase contact line
Young's equation relates the contact angle to interfacial tensions: γSV=γSL+γLVcosθ
γSV, γSL, and γLV represent the solid-vapor, solid-liquid, and liquid-vapor interfacial tensions, respectively
Wetting behavior is classified based on the contact angle:
Complete wetting: θ=0°, liquid spreads completely on the surface
Partial wetting: 0°<θ<90°, liquid partially spreads on the surface
Non-wetting: θ>90°, liquid tends to form droplets on the surface
Wettability is influenced by surface roughness, chemical heterogeneity, and surface energy
Roughness can enhance or reduce wettability depending on the surface chemistry
Chemical heterogeneity leads to contact angle hysteresis and pinning effects
Superhydrophobic surfaces exhibit extreme water repellency with contact angles greater than 150°
Achieved by combining surface roughness with low surface energy materials
Wetting transitions can occur due to changes in temperature, pressure, or surface chemistry
Examples include the transition from Cassie-Baxter state (droplet sitting on surface asperities) to Wenzel state (droplet penetrating surface asperities)
Capillarity and Its Applications
Capillarity describes the ability of a liquid to flow in narrow spaces without external forces
Capillary action is driven by the interplay between surface tension and adhesive forces
Liquid rises in a capillary tube when adhesive forces (liquid-solid) dominate cohesive forces (liquid-liquid)
Capillary rise height (h) is given by Jurin's law: h=ρgr2γcosθ
γ is the surface tension, θ is the contact angle, ρ is the liquid density, g is the acceleration due to gravity, and r is the capillary radius
Capillary pressure (Pc) is the pressure difference across a curved liquid-vapor interface
Described by the Young-Laplace equation: Pc=r2γcosθ
Capillarity plays a crucial role in various applications:
Wicking in porous media (paper, textiles, soils)
Ink delivery in printing processes
Oil recovery in petroleum engineering
Microfluidic devices for fluid transport and manipulation
Capillary fingering occurs when a less viscous fluid displaces a more viscous fluid in a porous medium
Leads to the formation of finger-like patterns and affects fluid displacement efficiency
Capillary condensation describes the condensation of vapor in confined spaces (pores, cracks) below the saturation vapor pressure
Governed by the Kelvin equation: lnP0P=rRT2γVmcosθ, where P is the vapor pressure, P0 is the saturation vapor pressure, Vm is the molar volume, R is the gas constant, and T is the temperature
Interfacial Forces in Multiphase Systems
Interfacial forces play a crucial role in the behavior and stability of multiphase systems
Surface tension forces arise from the imbalance of molecular forces at the interface
Act tangentially to the interface and minimize the surface area
Disjoining pressure is the pressure difference between a thin film and the bulk phase
Originates from intermolecular forces (van der Waals, electrostatic, steric) acting across the film
Contributes to the stability and thickness of thin films, such as soap films and liquid coatings
Capillary pressure is the pressure difference across a curved liquid-vapor interface
Determined by the Young-Laplace equation: Pc=γ(R11+R21)
Influences the shape and stability of droplets, bubbles, and menisci
Marangoni stresses arise from surface tension gradients along an interface
Caused by temperature, concentration, or surfactant gradients
Drive the movement of liquids from regions of low surface tension to high surface tension
Interfacial shear stresses develop when there is a relative motion between two immiscible fluids
Affect the flow behavior and mixing in multiphase systems
Interfacial forces influence the stability and rheology of emulsions, foams, and suspensions
Determine the droplet/bubble size distribution, coalescence, and phase separation
Interfacial instabilities (Rayleigh-Taylor, Kelvin-Helmholtz) can occur due to the interplay of interfacial forces and fluid properties
Lead to the breakup of interfaces and the formation of complex flow patterns
Measurement Techniques and Experimental Methods
Various techniques are employed to measure interfacial properties and study interfacial phenomena
Pendant drop method measures surface or interfacial tension by analyzing the shape of a suspended droplet
Droplet shape is determined by the balance between surface tension and gravitational forces
Wilhelmy plate method measures surface tension by measuring the force exerted on a vertically suspended plate partially immersed in a liquid
Surface tension is calculated from the measured force and the plate's perimeter
Du Noüy ring method measures surface or interfacial tension using a wire ring pulled through the interface
Maximum force required to detach the ring from the interface is related to the surface tension
Sessile drop method measures the contact angle of a liquid droplet on a solid surface
Droplet profile is analyzed using image processing techniques to determine the contact angle
Capillary rise method measures surface tension by measuring the height of liquid rise in a capillary tube
Surface tension is calculated using Jurin's law: h=ρgr2γcosθ
Spinning drop tensiometry measures ultralow interfacial tensions between two immiscible liquids
Droplet elongation in a rotating capillary is related to the interfacial tension
Langmuir-Blodgett trough studies the behavior of monolayers at the air-water interface
Measures surface pressure-area isotherms and provides insights into molecular packing and phase transitions
Brewster angle microscopy visualizes monolayers and thin films at interfaces without the need for labeling
Based on the principle of Brewster angle, where p-polarized light is not reflected from the interface
Modeling Approaches for Interfacial Phenomena
Modeling interfacial phenomena is essential for understanding and predicting the behavior of multiphase systems
Continuum models treat the interface as a sharp boundary separating two bulk phases
Governed by conservation equations and boundary conditions at the interface
Examples include the Volume of Fluid (VOF) method and the Level Set method
Sharp interface models explicitly track the interface and resolve its dynamics
Suitable for problems with well-defined interfaces and moderate interface deformations
Examples include the Front Tracking method and the Immersed Boundary method
Diffuse interface models represent the interface as a thin region with a smooth variation of properties
Capture interface dynamics through the evolution of an order parameter (phase-field variable)
Examples include the Phase-Field method and the Cahn-Hilliard equation
Molecular dynamics simulations model the behavior of individual molecules or particles
Provide insights into interfacial phenomena at the molecular scale
Suitable for studying adsorption, wetting, and interfacial structure
Lattice Boltzmann methods (LBM) simulate fluid flow and interfacial dynamics using a discrete kinetic approach
Capture interfacial physics through appropriate boundary conditions and force models
Smoothed particle hydrodynamics (SPH) is a meshless Lagrangian method for modeling fluid flow and interfacial phenomena
Particles carry fluid properties and interact through smoothing kernels
Hybrid models combine different modeling approaches to leverage their respective strengths
Examples include coupled VOF-LBM, Phase-Field-SPH, and Molecular Dynamics-Continuum methods
Model validation and comparison with experimental data are crucial for assessing the accuracy and predictive capability of interfacial models