Notes on Stress, Shear, and Viscosity: Newtonian and Non-Newtonian Fluids
Foundational quantities in solid mechanics and fluids
- Pressure and normal stress
- Pressure is the normal force per unit area: P = \frac{F}{A}
- In solid mechanics, this is viewed as normal stress (often denoted by sigma, \sigma)
- Stress is a tensor with multiple components; we also have shear stress (not just normal stress)
- Normal vs. shear stress
- Normal stress is perpendicular to a surface
- Shear stress is parallel to a surface: defined as the resistance to deformation due to shear force
- Shear stress is denoted by \tau (tau); common shorthand in class: tau for shear stress
- Example notation: \tau_{z}^{x} in an x,y,z coordinate system indicates shear stress in the x-direction on a surface with normal in the z-direction; the first footnote indicates the velocity-gradient direction, the second notes the direction of the shear force
- Units: shear stress has the same units as pressure (Pa in SI)
- Deformation under stress: solids vs fluids
- For solids: applying shear leads to deformation (shape changes) while the body resists; the deformation can be visualized as a stack of layers sliding relative to each other
- Strain (deformation measure) is percent deformation; for elongation, \varepsilon = \frac{\Delta L}{L_0}
- In fluids: fluids offer little resistance to permanent deformation; they flow; deformation is continuous under shear
- Viscosity is the mediator of shear-induced deformation in fluids; it links shear stress to the rate of deformation
- Shear stress vs deformation in fluids and the velocity gradient
- Shear rate (gamma dot) is the rate of shear deformation, i.e., velocity gradient
- Basic definition (simple shear in x-direction across y): \dot{\gamma} = \frac{du_x}{dy} (sometimes written as \frac{d u}{d y} depending on notation)
- Conceptual picture: adjacent fluid layers move with different velocities; the interaction between layers (intermolecular forces) governs the rate of momentum transfer and hence viscosity
- If the top layer is dragged faster than the layer below, momentum transfers downward and upward, with dissipation as heat due to intermolecular interactions
- The velocity gradient quantifies how different layers move; a larger gradient means larger shear rate and typically more shear stress for a given fluid
- Viscosity and the Newtonian constitutive relation
- Viscosity concept: a material property that describes how resistant a fluid is to shear and how it mediates the conversion of shear stress into deformation rate
- Constitutive relation (Newtonian fluids): \tau = \mu \dot{\gamma} where \dot{\gamma} is the shear rate and \mu is the dynamic viscosity
- The proportionality constant (viscosity) is assumed constant for Newtonian fluids (independent of the shear rate); for many real fluids, viscosity can depend on the shear rate (non-Newtonian behavior)
- Apparent viscosity: \mu{app} = \frac{\tau}{\dot{\gamma}}; if \mu{app} is constant across different shear stresses and shear rates, the fluid is Newtonian; if not, it is non-Newtonian
- In many liquids, especially simple liquids like water, the Newtonian linear relationship holds over a wide range; complex fluids (paints, starch suspensions, blood) often show non-Newtonian behavior
- Why the relationship is often first-order and linear (small-strain intuition)
- Consider an infinitesimally thin layer of fluid; for a very small strain, the change in angle and velocity can be related linearly to the applied shear stress
- For tiny deformations, \tan(\Delta\theta) \approx \Delta\theta, and the ratio \frac{\Delta u}{\Delta t} relates to the velocity gradient across a small separation \Delta y
- This leads to a proportionality between shear stress and velocity gradient in the infinitesimal limit, i.e., a linear constitutive relation with viscosity as the proportionality constant
- In many texts, this linear, first-order relation underpins the Newtonian model; deviations at high shear rates or for complex fluids yield non-Newtonian behavior
- Why viscosity is a constitutive property and its units
- Viscosity depends on the molecular structure and intermolecular interactions of the fluid; it is not a universal constant but a property of the material
- SI unit of dynamic viscosity: [\mu] = \text{Pa} \cdot \text{s} (or kg/(m·s))
- Some alternate units include poise (P) and centipoise (cP): 1 Pa·s = 10 Poise; 1 cP = 0.001 Pa·s
- Typical viscosity values for common fluids (at around room temperature unless stated otherwise)
- Water: \mu \approx 1.0 \times 10^{-3} \text{ Pa}\cdot\text{s}
- Air: about two orders of magnitude smaller than water; commonly quoted around \mu_{air} \sim 1.8 \times 10^{-5} \text{ Pa}\cdot\text{s} (roughly 10^(-5) to 10^(-5) range)
- Plasma (component of blood): similar to water, slightly higher; roughly \mu_{plasma} \approx 1.2 \text{ cP} = 1.2 \times 10^{-3} \text{ Pa}\cdot\text{s}
- Blood: viscosity depends on hematocrit (cell concentration); large-vessel viscosity around \mu_{blood} \approx 4 \text{ cP} = 4 \times 10^{-3} \text{ Pa}\cdot\text{s} at 37°C ~ hematocrit ≈ 45%
- Kinematic viscosity and momentum diffusivity
- Kinematic viscosity: \nu = \frac{\mu}{\rho} where \rho is density
- Units: \nu has units of \text{m}^2/\text{s}; describes diffusivity of momentum instead of momentum per unit area per unit time
- Relationship: for a given fluid, higher density lowers the kinematic viscosity for the same dynamic viscosity
- Practical demos and contexts to connect concepts
- Torque converters and lubricants: viscous fluids (oil) enable momentum transfer and heat removal in transmissions; oil’s viscosity is central to coupling momentum and cooling
- The role of viscosity in everyday devices and engineering systems: viscosity affects how momentum is transmitted and dissipated as heat or used for coupling
- Special case: viscosity at very low temperatures (helium experiments and two-fluid model)
- Helium II (superfluid phase below lambda point): demonstrates a paradox where capillary flow appears to show zero viscosity, while a rotating cylinder reveals a finite (normal) component with viscosity
- Two-fluid model for He II: normal component with viscosity that drags with macroscopic flow, and superfluid component with essentially zero viscosity that can flow through very narrow channels with no resistance
- Capillary flow experiments show normal component controls resistance in narrow capillaries; rotating-cylinder experiments reveal the normal component’s viscosity; the superfluid component does not participate in the slow, viscous transport in the capillaries
- This duality leads to the concept that He II behaves as two interpenetrating fluids: a normal viscous component and a zero-viscosity superfluid component
- Temperature dependence and limits of viscosity
- As temperature approaches absolute zero, molecular motion drops; classical viscosity tends toward zero but a residual viscosity can persist due to quantum and other effects in real systems
- In classical fluids, viscosity is generally nonzero at finite temperatures because molecules continually interact
- Non-Newtonian fluids: definitions and examples
- Apparent viscosity concept: \mu_{app} = \frac{\tau}{\dot{\gamma}}
- Newtonian fluid: \mu_{app} is constant regardless of the applied shear stress or shear rate
- Non-Newtonian fluid: \mu_{app} changes with shear rate or shear stress; viscosity is not constant
- Everyday examples
- Paints: polymer particles in water; mixing paint initially hard; as shear rate increases, viscosity decreases (shear-thinning) or sometimes complicates behavior depending on formulation
- Starch suspensions: nonlinear and can be shear-thickening (viscosity increases with shear rate) in some systems
- Blood: viscosity depends on hematocrit (cell concentration) due to interactions and collisions among cells; higher hematocrit -> higher viscosity
- Non-slip boundary conditions (mention for later)
- Boundary conditions in fluid mechanics; non-slip condition states that fluid velocity at a solid boundary equals the boundary velocity (often zero for stationary walls)
- Will be discussed further in subsequent topics
- Connections to broader themes and practical implications
- Viscosity connects to energy dissipation, heat generation, and momentum transport in fluids
- Viscosity is central to fluid design in pipelines, lubrication, microfluidics, and biological systems (blood flow, capillary transport)
- The concept of Newtonian vs non-Newtonian fluids helps explain why some real-world fluids behave counterintuitively under different flow conditions (e.g., paints that become easier to stir at high speeds, starch suspensions that stiffen with rapid stirring)
- Quick glossary of key notations and concepts used in this material
- Pressure: P = \frac{F}{A}
- Normal stress: \sigma
- Shear stress: \tau
- Shear rate: \dot{\gamma}; often \dot{\gamma} = \dfrac{du}{dy} in simple shear
- Dynamic viscosity: \mu; unit \text{Pa}\cdot\text{s}
- Kinematic viscosity: \nu = \dfrac{\mu}{\rho}; unit \text{m}^2/\text{s}
- Relationship between shear stress and rate: \tau = \mu \dot{\gamma} (Newtonian)
- Apparent viscosity: \mu_{app} = \dfrac{\tau}{\dot{\gamma}}
- Strain (solid deformation): \varepsilon = \frac{\Delta L}{L_0}
- Capillary flow in helium: He I (normal viscous), He II (two-fluid: normal component with viscosity + superfluid with zero viscosity), capillary vs rotating-cylinder experiments
- Summary takeaway
- Stress, strain, and viscosity are core concepts for connecting forces to deformations in solids and fluids
- Viscosity acts as the mediator between shear stress and velocity gradients in fluids; it is a material property that can be constant (Newtonian) or depend on shear rate (non-Newtonian)
- Momentum diffusion in fluids is characterized by viscosity and, in the case of momentum diffusion in fluids, by the related kinematic viscosity; real fluids exhibit a rich set of behaviors from simple Newtonian to complex non-Newtonian and quantum fluids (e.g., helium II)