Constitutive equation

In physics, a constitutive equation is a relation between two physical quantities (especially kinetic quantities are related to kinematic quantities) that is specific to a material or substance, and approximates the response of that material to external forces. It is combined with other equations governing physical laws to solve physical problems, like the flow of a fluid in a pipe, or the response of a crystal to an electric field.

As an example, in structural analysis, constitutive relations connect applied stresses or forces to strains or deformations. The stress-strain constitutive relation for linear materials is commonly known as Hooke's law.

Some constitutive equations are simply phenomenological; others are derived from first principles. A common approximate constitutive equation frequently is expressed as a simple proportionality using a parameter taken to be a property of the material, such as electrical conductivity or a spring constant. However, much more elaborate constitutive equations often are necessary to account for tensor properties, the rate of response of materials and their non-linear behavior.[1] See the article Linear response function.

The first constitutive equation (constitutive law) was developed by Robert Hooke and is known as Hooke's law. It deals with the case of linear elastic materials. Following this discovery, this type of equation, often called a "stress-strain relation" in this example, but also called a "constitutive assumption" or an "equation of state" was commonly used. Walter Noll advanced the use of constitutive equations, clarifying their classification and the role of invariance requirements, constraints, and definitions of terms like "material", "isotropic", "aeolotropic", etc. The class of "constitutive relations" of the form stress rate = f (velocity gradient, stress, density) was the subject of Walter Noll's dissertation in 1954 under Clifford Truesdell.[2]

In modern condensed matter physics, the constitutive equation plays a major role. See Linear constitutive equations and Nonlinear correlation functions.[3]

Following are numerous examples of constitutive equations, many in frequent use.

Contents

Matter

Definitions

Nomenclature
F = friction force (N)

R = reaction force at point of contact (N)

Quantity (Common Name/s) (Common) Symbol/s Defining Equation SI Units Dimension
Static, kinetic, and rolling friction coefficients μ, μf F \leqslant \mu_\mathrm{static} R \,

F = \mu_\mathrm{kinetic} R \,
F = \mu_\mathrm{roll} R \,

Normal force to a surface:
F_\bot = \mathbf{F}\cdot\mathbf{\hat{n}}\,\!

dimensionless dimensionless

Definitive laws

Property/effect Equation
Hooke's law, defines elasticity/spring constants Scalar forms: F_i=-k x_i \,

or \sigma = Y \, \epsilon \, 

Tensor forms,  \sigma_{ij} = C_{ijkl} \, \epsilon_{kl} \, 
or inversely,  \epsilon_{ij} = S_{ijkl} \, \sigma_{kl} \,

F = tensile/compressive force (N)

x = extended/contracted displacement (m)
σ = stress (Pa)
ε = strain (dimensionless)
k = (Hooke's Law) spring constant (N m−1)
Y = Young's modulus (Pa)
C = elasticity tensor (Pa)
S = compliance tensor (dimensionless)

Newton's law of experimental impact, defines coefficient of restitution  e = \frac{\left | \mathbf{v} \right | _\mathrm{separation}}{\left | \mathbf{v} \right | _\mathrm{approach}} \,\!

Usually  0 \leqslant e \leqslant 1 \,\! ,
but it is possible that  e \geqslant 1 \,\!

e = Coefficient of restitution

vseparation = relative velocity of separation (m s−1)
vapproach = relative velocity of approach (m s−1)

Transport phenomena

Nomenclature
x = displacement of substance(m)

A = Cross-section Area(m2)
v = Flow velocity (m s−1)
μ = Fluid viscosity (Pa s) Fd = Drag force (N)
g = Standard gravitational acceleration = 9.81 N kg-1
ρ = Volume mass density of fluid (kg m−3)

Definitions

Quantity (Common Name/s) (Common) Symbol/s Defining Equation SI Units Dimension
Drag equation, drag coefficient cd F_d = \frac{1}{2}c_d \rho A v^2 \, dimensionless dimensionless

Definitive laws

Property/effect Equation
Fick's law of diffusion, defines diffusion coefficient D  J_j = - D_{ij} \frac{\partial C}{\partial x_i}
D = mass diffusion coefficient (m2 s−1)

J = diffusion flux of substance (mol m−2 s−1)
C/∂x = (1d)concentration gradient of substance (mol dm−4)

Darcy's law for porous flow in matter, defines permeability κ  q_j = -\frac{\kappa}{\mu} \frac{\partial P}{\partial x_j}
κ = permeability of medium (m2)

q = discharge flux of substance (m s−1)
P/∂x = (1d) pressure gradient of system (Pa m−1)

Equations

Property/effect Equation
Terminal velocity v_t = \sqrt{\frac{2 F_d g}{c_d \rho \mathbf{A} \cdot \mathbf{\hat{n}}}} \,
vt = terminal velocity within fluid (m s-1)
Newtonian fluid \tau = \mu \frac {\partial u}{\partial y} \,
τ = shear stress exerted by fluid (Pa)

u/∂y = velocity gradient perp. to shear direction, strain rate (s−1)

Thermodynamics

Nomenclature
L = length of material (m)

Δx = Displacement of heat transfer (m)
A = surface cross section (m2)
V = Volume (m3)

T = Temperature (K)
T = temperature gradient (K m−1)
q = heat energy (J)
P = thermal current, thermal power (W)
ε = strain or emmisivity (both dimensionless)

Definitions

Quantity (Common Name/s) (Common) Symbol/s Defining Equation SI Units Dimension
General heat capacity C = Heat capacity q = C T \, J K−1
Linear thermal expansion α = Linear coefficient of linear thermal expansion  \partial L/\partial T = \alpha L \,\!

\epsilon_{ij} = \alpha_{ij}\Delta T \,

K−1 [Θ]−1
Volumetric thermal expansion β, γ  \partial V/\partial T = \beta V \,\! K−1
Thermal conductivity κ, K, λ  \lambda = - P/\left (\mathbf{A} \cdot \nabla T \right ) \,\! W m−1 K−1
Thermal conductance U  U = \lambda/\delta x \,\! W m−2 K−1
Thermal resistance R R=1/U=\Delta x/\lambda\,\! m2 K W−1

Definitive laws

Property/effect Equation
Fourier's law of thermal conduction, defines thermal conductivity λ  q_j= - \lambda_{ij}\frac{\partial T}{\partial x_i} \,
λ = Thermal conductivity (W m−1 K−1 )

q = heat flux (W m−2)
T/∂x = (1d) Temperature gradient (K m−1)

Stefan–Boltzmann law of black-body radiation, defines emmisivity ε For a single radiator:

I = \epsilon \sigma T^4\,

For a temperature differance:
I = \epsilon \sigma \left ( T_\mathrm{ext}^4 - T_\mathrm{sys}^4 \right ) \,

 0 \leqslant \epsilon \leqslant 1\,\!
 \epsilon = 0\,\! for perfect reflector
 \epsilon = 1\,\! for perfect absorber (true black body)

I = radiant intensity (W m−2)

σ = Stefan–Boltzmann constant (W m−2 K−4)
Tsys = temperature of radiating system(K)
Text = temperature of external surroundings (K)
T = temperature (K)
ε = emissivity (dimensionless)

Ideal gas law, defines parameters of an ideal gas pV = nRT\,
p = pressure (Pa)

T = temperature (K)
V = volume (m−3)
R = gas constant (J K−1 mol−1)
n = number of moles, amount of substance (mol)

Electromagnetism

Constitutive equations in electromagnetism and related areas

In both classical and quantum physics, the precise dynamics of a system form a set of coupled differential equations, which are almost always too complicated to be solved exactly, even at the level of statistical mechanics. In the context of electromagnetism, this remark applies to not only the dynamics of free charges and currents (which enter Maxwell's equations directly), but also the dynamics of bound charges and currents (which enter Maxwell's equations through the constitutive relations). As a result, various approximation schemes are typically used.

For example, in real materials, complex transport equations must be solved to determine the time and spatial response of charges, for example, the Boltzmann equation or the Fokker–Planck equation or the Navier-Stokes equations. For example, see magnetohydrodynamics, fluid dynamics, electrohydrodynamics, superconductivity, plasma modeling. An entire physical apparatus for dealing with these matters has developed. See for example, linear response theory, Green–Kubo relations and Green's function (many-body theory).

These complex theories provide detailed formulas for the constitutive relations describing the electrical response of various materials, such as permittivities, permeabilities, conductivities and so forth.

Nomenclature
E = electric field (N C−1)

D = electric displacement field (Cm−2)
P = polarization density (C m−2)
B = magnetic flux density, induction field (T = N A−1 m−1)
H = magnetic field intensity (A m−1)
M = magnetization field (A m−1)

Definitions

Quantity (Common Name/s) (Common) Symbol/s Defining Equation SI Units Dimension
Electrical resistance R R = V/I \,\! Ω = V A−1 = J s C−2 [M] [L]2 [T]−3 [I]−2
Resistivity ρ \rho = RA/l \,\! Ω m [M]2 [L]2 [T]−3 [I]−2
Resistivity temperature coefficient, linear temperature dependence α \rho - \rho_0 = \rho_0\alpha(T-T_0)\,\! K−1 [Θ]−1
Electrical conductance G  G = 1/R \,\! S = Ω−1 [T]3 [I]2 [M]−1 [L]−2
Electrical conductivity σ \sigma = 1/\rho \,\! Ω−1 m−1 [I]2 [T]3 [M]−2 [L]−2
Relative permittivity (aka dielectric constant) εr can only be found from experiment F m−1 [I]2 [T]4 [M]−1 [L]−3
(Absolute) dielectric permittivity ε  D_j = \epsilon_{ji} E_i \, F m−1 [I]2 [T]4 [M]−1 [L]−3
Electric susceptibility χE P_j =  \epsilon_0 \left ( \chi_E \right )_{ji} E_i \, dimensionless dimensionless
Magnetic reluctance R, Rm, \mathcal{R} R_\mathrm{m} = \mathcal{M}/\Phi_B A Wb-1 = H-1 [M]-1[L]-2[T]2
Magnetic permeance P, Pm, Λ, \mathcal{P} \Lambda = 1/R_\mathrm{m} Wb A-1 = H [M][L]2[T]-2
Relative permeability μr can only be found from experiment dimensionless dimensionless
Absolute magnetic permeability μ B_j =  \mu_{ji} H_i \, H m−1
Magnetic susceptibility χM M_j =  \left ( \chi_M \right )_{ji} H_i \, dimensionless dimensionless

Relations

Property/effect Equation
Electric field vectors  E_i = \frac{1}{\epsilon } D_i = \frac{1}{\epsilon_0} \left ( D_i - P_i \right )\,
Magnetic field Vectors  B_i = \mu H_i = \mu_0 \left ( H_i %2B M_i \right ) \,
Permittivity  \epsilon/\epsilon_0 = \epsilon_r = \left ( \chi_E %2B 1 \right )\,\!
Permeability  \mu / \mu_0 = \mu_r = \left ( \chi_M %2B 1 \right ) \,\!

Laws

Property/effect Equation
Ohm's law of electric conduction,

defines electric conductivity (and so resistivity and resistance)

Simplist form is:  V = IR \,

More general forms are:
J_j = \sigma_{ji} E_i \,
E_j = \rho_{ji} J_i \,

J = Electric Current Density (A m−2)

σ = Electric Conductivity−1 m−1)
ρ = Electrical resistivity (Ω m)

Photonics

Nomenclature
c = luminal speed in medium (m s−1)

c0 = luminal speed in vacuum (m s−1)
ε = electric permittivity of medium (F m−1)
ε0 = vacuum electric permittivity (F m−1)
εr = relative electric permittivity of medium (F m−1)
μ = magnetic permeability of medium (H m−1)
μ0 = vacuum magnetic permeability (H m−1)
μr = relative magnetic permeability of medium (H m−1)

Definitions

Quantity (Common Name/s) (Common) Symbol/s Defining Equation SI Units Dimension
Refractive index n  n = \frac{c}{c_0} = \sqrt{\frac{\epsilon_0 \mu_0}{\epsilon \mu}} = \sqrt{\epsilon_r \mu_r} \, dimensionless dimensionless

Relations

Property/effect Equation
Luminal speed in matter  c = 1/\sqrt{\epsilon \mu} \,

for special case of vacuum; ε = ε0 and μ = μ0,
 c_0 = 1/ \sqrt{\epsilon_0\mu_0} \,

Solid state physics

These constitutive equations are often used in crystallography - a field of solid state physics.[4]

Nomenclature
x = displacement (m)

s = thickness of hall/probe (m)

σ = mechanical stress (Pa)
ε = mechanical strain (dimensionless)

e = electron charge (C)
n = charge carrier density E = electric field (N C−1)
D = electric displacement field (Cm−2)
P = dielectric polarization density (C m−2)
B = magnetic flux density, induction field (T = N A−1 m−1)
H = Magnetic Field Intensity (A m−1)
M = magnetization field (A m−1)
I = electric current (across Hall plate) (A) J = electric current density (A m−2)
ρ = electrical resistivity (Ω m) a = dielectric impermeability (K)
VH = Hall voltage (V)

T = temperature (K)
S = entropy (J K−1)
q = heat flux (W m−2)

Definitions

Quantity (Common Name/s) (Common) Symbol/s Defining Equation SI Units Dimension
Pyroelectricity, pyroelectric coefficient p  \Delta P_j = p_{j} \Delta T \, C m−2 K−1
Electrocaloric effect, pyroelectric coefficient p  \Delta S = p_{i} \Delta E_i \, C m−2 K−1 [I][T][L]-2[Θ]-1
Seebeck effect, thermopower coefficient β  E_{i} = - \beta_{ij} \frac{\partial T}{\partial x_j} \, V K−1
Hall effect, Hall coefficient RH R_H =\frac{E_y}{J_xB}= \frac{sV_H}{IB}=-\frac{1}{ne} C-1 [I]-1[T]-1
Peltier effect, peltier coefficient Π  q_{j} = \Pi_{ji} J_{i} \, W A−1
Direct piezoelectric effect, direct piezoelectric coefficient d, de P_{i} = \left ( d_\mathrm{e} \right )_{ijk}\sigma_{jk} \, K−1
Converse piezoelectric effect, direct piezoelectric coefficient d, de' \epsilon_{ij} = \left ( d_\mathrm{e'} \right )_{ijk}E_{k} \, K−1
Piezomagnetic effect, piezomagnetic coefficient q, dm M_{i} = \left ( d_\mathrm{m} \right )_{ijk}\sigma_{jk} \, K−1
Piezooptic effect, piezooptic coefficient Π a_{ij} = \Pi_{ijpq}\sigma_{pq} \, K−1

Equations

Property/effect Equation
Hall effect  E_{k} = \rho_{kij} J_{i} H_j \,

See also

References

  1. ^ Clifford Truesdell & Walter Noll; Stuart S. Antman, editor (2004). The Non-linear Field Theories of Mechanics. Springer. p. 4. ISBN 3540027793. http://books.google.com/books?id=dp84F_odrBQC&pg=PR13&dq=%22Preface+%22+inauthor:Antman. 
  2. ^ See Truesdell's account in Truesdell The naturalization and apotheosis of Walter Noll. See also Noll's account and the classic treatise by both authors: Clifford Truesdell & Walter Noll - Stuart S. Antman (editor) (2004). "Preface" (Originally published as Volume III/3 of the famous Encyclopedia of Physics in 1965). The Non-linear Field Theories of Mechanics (3rd ed.). Springer. p. xiii. ISBN 3540027793. http://books.google.com/books?id=dp84F_odrBQC&pg=PR13&dq=%22Preface+to+the+Third%22+inauthor:Antman. 
  3. ^ Jørgen Rammer (2007). Quantum Field Theory of Nonequilibrium States. Cambridge University Press. ISBN 9780521874991. http://books.google.com/books?id=A7TbrAm5Wq0C&pg=PR1&dq=isbn:9780521874991#PPA151,M1. 
  4. ^ http://www.mx.iucr.org/iucr-top/comm/cteach/pamphlets/18/node2.html

External links