Hydrodynamic limit in the Hyperbolic Space-Time Scale Stefano Olla - - PowerPoint PPT Presentation

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Hydrodynamic limit in the Hyperbolic Space-Time Scale Stefano Olla - - PowerPoint PPT Presentation

Hydrodynamic limit in the Hyperbolic Space-Time Scale Stefano Olla CEREMADE, Universit e Paris-Dauphine, PSL Supported by ANR LSD Firenze September 14, 2018 S. Olla - CEREMADE hyperbolic limits Hydrodynamic Scaling Limits Dynamics


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Hydrodynamic limit in the Hyperbolic Space-Time Scale

Stefano Olla CEREMADE, Universit´ e Paris-Dauphine, PSL

Supported by ANR LSD

Firenze September 14, 2018

  • S. Olla - CEREMADE

hyperbolic limits

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Hydrodynamic Scaling Limits

▸ Dynamics with conserved quantities: energy, momentum,

density, ..., these move slowly.

  • S. Olla - CEREMADE

hyperbolic limits

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Hydrodynamic Scaling Limits

▸ Dynamics with conserved quantities: energy, momentum,

density, ..., these move slowly.

▸ The other quantities move fast, fluctuating around average

values determined by the conserved quantities (by local equilibriums).

  • S. Olla - CEREMADE

hyperbolic limits

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Hydrodynamic Scaling Limits

▸ Dynamics with conserved quantities: energy, momentum,

density, ..., these move slowly.

▸ The other quantities move fast, fluctuating around average

values determined by the conserved quantities (by local equilibriums).

▸ Conserved quantities determine families of stationary

probability measures, Gibbs states, typically parametrized by temperature, pressure.

  • S. Olla - CEREMADE

hyperbolic limits

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Hydrodynamic Scaling Limits

▸ Dynamics with conserved quantities: energy, momentum,

density, ..., these move slowly.

▸ The other quantities move fast, fluctuating around average

values determined by the conserved quantities (by local equilibriums).

▸ Conserved quantities determine families of stationary

probability measures, Gibbs states, typically parametrized by temperature, pressure.

▸ Corresponding to different paramenters there are different

partial equilibriums:

▸ mechanical equilibrium: constant pressure or tension profiles, ▸ thermal equilibrium: constant temperature profiles.

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Hydrodynamic Scaling Limits

▸ Dynamics with conserved quantities: energy, momentum,

density, ..., these move slowly.

▸ The other quantities move fast, fluctuating around average

values determined by the conserved quantities (by local equilibriums).

▸ Conserved quantities determine families of stationary

probability measures, Gibbs states, typically parametrized by temperature, pressure.

▸ Corresponding to different paramenters there are different

partial equilibriums:

▸ mechanical equilibrium: constant pressure or tension profiles, ▸ thermal equilibrium: constant temperature profiles.

▸ These partial equilibriums may be reached at different time

scales: typically mechanical equilibrium is reached faster than thermal equilibrium.

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Mechanical and Thermal equilibrium

▸ Mechanical Equilibrium is reached in hyperbolic time scales

(same rescaling of space and time), and is driven by Euler system of equations (for a compressible gas). It involves the ballistic evolution of the long waves (mechanical modes).

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Mechanical and Thermal equilibrium

▸ Mechanical Equilibrium is reached in hyperbolic time scales

(same rescaling of space and time), and is driven by Euler system of equations (for a compressible gas). It involves the ballistic evolution of the long waves (mechanical modes).

▸ When thermal conductivity is finite, Thermal Equilibrium is

reached later, in the diffusive time scales (time2 = space), and temperature (or thermal energy) profiles evolve following heat equation.

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Mechanical and Thermal equilibrium

▸ Mechanical Equilibrium is reached in hyperbolic time scales

(same rescaling of space and time), and is driven by Euler system of equations (for a compressible gas). It involves the ballistic evolution of the long waves (mechanical modes).

▸ When thermal conductivity is finite, Thermal Equilibrium is

reached later, in the diffusive time scales (time2 = space), and temperature (or thermal energy) profiles evolve following heat equation.

▸ If thermal conductivity is infinite, Thermal Equilibrium is

reached in a super-diffusive time scales (timeα = space,α < 2), and typically temperature (or thermal energy) profiles evolve following a fractional heat equation.

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Boundary Conditions

Extermal forces or heat bath acting microscopically at the boudary

  • n the system determine boundary conditions of the macroscopic

equations.

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Boundary Conditions

Extermal forces or heat bath acting microscopically at the boudary

  • n the system determine boundary conditions of the macroscopic

equations. Most of non-equilibrium situation are obtained by

▸ changing boundary conditions in time

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Boundary Conditions

Extermal forces or heat bath acting microscopically at the boudary

  • n the system determine boundary conditions of the macroscopic

equations. Most of non-equilibrium situation are obtained by

▸ changing boundary conditions in time ▸ applying boundary conditions corresponding to different

equilibrium states, obtaining dynamics that have non-equilibrium stationary states (NESS).

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Chain of oscillators

˙ rx(t) = px(t) − px−1(t), x = 1,...,N ˙ px(t) = V ′(rx+1(t)) − V ′(rx(t)) x = 1,...,N − 1 ˙ pN(t) = τ(t/N) − V ′(rN(t)) p0(t) = 0.

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Chain of oscillators

˙ rx(t) = px(t) − px−1(t), x = 1,...,N ˙ px(t) = V ′(rx+1(t)) − V ′(rx(t)) x = 1,...,N − 1 ˙ pN(t) = τ(t/N) − V ′(rN(t)) p0(t) = 0. E E Ex = p2

x

2 + V (rx) ˙ E E Ex = pxV ′(rx+1) − px−1V ′(rx)

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Chain of oscillators

˙ rx(t) = px(t) − px−1(t), x = 1,...,N ˙ px(t) = V ′(rx+1(t)) − V ′(rx(t)) x = 1,...,N − 1 ˙ pN(t) = τ(t/N) − V ′(rN(t)) p0(t) = 0. E E Ex = p2

x

2 + V (rx) ˙ E E Ex = pxV ′(rx+1) − px−1V ′(rx) We are interested in the macroscopic evolution of (rx(t),px(t),E E Ex(t)).

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Gibbs measures and Thermodynamic Entropy

For τ(t) = τ constant in time, a class of stationary measures is given by the Gibbs measures at temperature β−1, tension τ dµβ,τ,p =

N

x=1

e−β(E

E Ex−τrx)−G(β,τ)dpxdrx

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Gibbs measures and Thermodynamic Entropy

For τ(t) = τ constant in time, a class of stationary measures is given by the Gibbs measures at temperature β−1, tension τ dµβ,τ,p =

N

x=1

e−β(E

E Ex−τrx)−G(β,τ)dpxdrx

Thermodynamic entropy is S(u,r) = inf

τ,β {−βτr + βu − G(β,τ)}

β(u,r) = ∂uS(u,r), τ(u,r) = −β−1∂rS(u,r).

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Ergodicity (of the infinite system)

Consider the corresponding infinite dynamics: ˙ rx(t) = px(t) − px−1(t), ˙ px(t) = V ′(rx+1(t)) − V ′(rx(t)) x ∈ Z

Theorem

(Fritz, Funaki, Lebowitz, PTRF 1994) Assume that a probability ν is translation invariant, stationary, finite entropy density, and the conditional measure ν(dp∣r) is exchangeable. Then ν is a convex combination of Gibbs measures dµβ,τ,p.

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Ergodicity (of the infinite system)

Consider the corresponding infinite dynamics: ˙ rx(t) = px(t) − px−1(t), ˙ px(t) = V ′(rx+1(t)) − V ′(rx(t)) x ∈ Z

Theorem

(Fritz, Funaki, Lebowitz, PTRF 1994) Assume that a probability ν is translation invariant, stationary, finite entropy density, and the conditional measure ν(dp∣r) is exchangeable. Then ν is a convex combination of Gibbs measures dµβ,τ,p.

▸ Chaoticity of the dynamics, due to the non-linearity of V ,

should give such ergodic property

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Ergodicity (of the infinite system)

Consider the corresponding infinite dynamics: ˙ rx(t) = px(t) − px−1(t), ˙ px(t) = V ′(rx+1(t)) − V ′(rx(t)) x ∈ Z

Theorem

(Fritz, Funaki, Lebowitz, PTRF 1994) Assume that a probability ν is translation invariant, stationary, finite entropy density, and the conditional measure ν(dp∣r) is exchangeable. Then ν is a convex combination of Gibbs measures dµβ,τ,p.

▸ Chaoticity of the dynamics, due to the non-linearity of V ,

should give such ergodic property

▸ Adding conservative noise (stochastic collisions) to the

dynamics one obtain ergodicity.

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Hyperbolic Scaling, Euler equations

3 conserved quantities: we expect the weak convergence to the hyperbolic system of PDE 1 N ∑

x

G(x/N) ⎛ ⎜ ⎝ rx(Nt) px(Nt) Ex(Nt) ⎞ ⎟ ⎠

N→∞ ∫ 1 0 G(y)

⎛ ⎜ ⎝ r(y,t) p(y,t) e(y,t) ⎞ ⎟ ⎠ dy ∂tr(t,y) = ∂yp(t,y) ∂tp(t,y) = ∂yτ[u(t,y),r(t,y)] ∂te(t,y) = ∂y(τ[u(t,y),r(t,y)]p(t,y)) where u = e − p2/2 : internal energy. and, for smooth solutions, the boundary conditions: p(t,0) = 0, τ[u(t,1),r(t,1)] = τ(t)

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Euristics

take G ∶ [0,1] → R with compact support in (0,1), d dt 1 N ∑

x

G(x/N) ⎛ ⎜ ⎝ rx(Nt) px(Nt) Ex(Nt) ⎞ ⎟ ⎠ = ∑

x

G(x/N) ⎛ ⎜ ⎝ ∇px−1(Nt) ∇V ′(rx(Nt)) ∇[px(Nt)V ′(rx(Nt)] ⎞ ⎟ ⎠ ∼ − 1 N ∑

x

G ′(x/N) ⎛ ⎜ ⎝ px(Nt) V ′(rx(Nt)) px(Nt)V ′(rx(Nt) ⎞ ⎟ ⎠

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Euristics

take G ∶ [0,1] → R with compact support in (0,1), d dt 1 N ∑

x

G(x/N) ⎛ ⎜ ⎝ rx(Nt) px(Nt) Ex(Nt) ⎞ ⎟ ⎠ = ∑

x

G(x/N) ⎛ ⎜ ⎝ ∇px−1(Nt) ∇V ′(rx(Nt)) ∇[px(Nt)V ′(rx(Nt)] ⎞ ⎟ ⎠ ∼ − 1 N ∑

x

G ′(x/N) ⎛ ⎜ ⎝ px(Nt) V ′(rx(Nt)) px(Nt)V ′(rx(Nt) ⎞ ⎟ ⎠ assuming local equilibrium, we have ∼ −∫

1 0 G ′(y)

⎛ ⎜ ⎝ p(t,y) τ(u(t,y),r(t,y)) p(t,y)τ(u(t,y),r(t,y)) ⎞ ⎟ ⎠ dy Note that y ∈ [0,1] is the material (Lagrangian) coordinate.

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Results with conservative stochastic dynamics

▸ To prove some form of local equilibrium we need to add

stochastic terms to the dynamics (the deterministic non-linear case is too difficult).

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Results with conservative stochastic dynamics

▸ To prove some form of local equilibrium we need to add

stochastic terms to the dynamics (the deterministic non-linear case is too difficult).

▸ Random exchanges of velocities between nearest neighbor

particles, conserve energy, momentum and volume, destroying all other (possible) conservation laws. It provides the right ergodicity property.

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Results with conservative stochastic dynamics

▸ To prove some form of local equilibrium we need to add

stochastic terms to the dynamics (the deterministic non-linear case is too difficult).

▸ Random exchanges of velocities between nearest neighbor

particles, conserve energy, momentum and volume, destroying all other (possible) conservation laws. It provides the right ergodicity property.

▸ With such noise in the dynamics, for smooth solutions the HL

is proven in:

▸ N. Even, S.O., ARMA (2014) (with boundary conditions), ▸ S.O., SRS Varadhan, HT Yau, CMP (1993) (periodic bc).

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Harmonic Oscillators Chain

This is an example of a non-ergodic dynamics: V (r) = r2/2 in fact it is a completely integrable dynamics: ˙ qx = px, ˙ px = ∆qx = qx+1 + qx−1 − qx,

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Harmonic Oscillators Chain

This is an example of a non-ergodic dynamics: V (r) = r2/2 in fact it is a completely integrable dynamics: ˙ qx = px, ˙ px = ∆qx = qx+1 + qx−1 − qx, Take here x = 1,...,N, ˆ f (k) = ∑

x

fxei2πkx k ∈ {0,1/N,...,(N − 1)/N} ω(k) = 2∣sin(πk)∣ dispersion relation: H = ∑

x

E E Ex = 1 2N ∑

k

[ω(k)2∣ˆ q(k)∣2 + ∣ˆ p(k)∣2]

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Harmonic Oscillators Chain

This is an example of a non-ergodic dynamics: V (r) = r2/2 in fact it is a completely integrable dynamics: ˙ qx = px, ˙ px = ∆qx = qx+1 + qx−1 − qx, Take here x = 1,...,N, ˆ f (k) = ∑

x

fxei2πkx k ∈ {0,1/N,...,(N − 1)/N} ω(k) = 2∣sin(πk)∣ dispersion relation: H = ∑

x

E E Ex = 1 2N ∑

k

[ω(k)2∣ˆ q(k)∣2 + ∣ˆ p(k)∣2] ˆ ψ(t,k) ∶= ω(k)ˆ q (t,k) + i ˆ p (t,k).

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Harmonic Oscillators Chain

This is an example of a non-ergodic dynamics: V (r) = r2/2 in fact it is a completely integrable dynamics: ˙ qx = px, ˙ px = ∆qx = qx+1 + qx−1 − qx, Take here x = 1,...,N, ˆ f (k) = ∑

x

fxei2πkx k ∈ {0,1/N,...,(N − 1)/N} ω(k) = 2∣sin(πk)∣ dispersion relation: H = ∑

x

E E Ex = 1 2N ∑

k

[ω(k)2∣ˆ q(k)∣2 + ∣ˆ p(k)∣2] ˆ ψ(t,k) ∶= ω(k)ˆ q (t,k) + i ˆ p (t,k). d dt ˆ ψ(t,k) = −iω(k) ˆ ψ(t,k) ˆ ψ(t,k) = e−iω(k)t ˆ ψ(0,k)

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Harmonic Oscillators Chain: Quantum Dynamics

px = −i∂qx = −i (∂rx+1 − ∂rx) E E Ex = 1 2 (p2

x + r2 x )

ak = 1 ω(k) ˆ ψ(k), a∗

k =

1 ω(k) ˆ ψ(k)∗ H = ∑

x

E E Ex = 1 2N ∑

k

[ω(k)2∣ˆ q(k)∣2 + ∣ˆ p(k)∣2] = 1 2N ∑

k

ω(k)a∗

kak

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Harmonic Oscillators Chain: Quantum Dynamics

px = −i∂qx = −i (∂rx+1 − ∂rx) E E Ex = 1 2 (p2

x + r2 x )

ak = 1 ω(k) ˆ ψ(k), a∗

k =

1 ω(k) ˆ ψ(k)∗ H = ∑

x

E E Ex = 1 2N ∑

k

[ω(k)2∣ˆ q(k)∣2 + ∣ˆ p(k)∣2] = 1 2N ∑

k

ω(k)a∗

kak

Heisenber evolution d

dt A(t) = i[H,A(t)]

ak(t) = e−iω(k)tak, a∗

k(t) = e−iω(k)ta∗ k.

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Harmonic Chain: Thermal Equilibrium (Classic case)

Consider the chain in thermal equilibrium: initial distribution with covariances ⟨ ⟨ ⟨ rx(0);rx′(0) ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ px(0);px′(0) ⟩ ⟩ ⟩ = β−1δx,x′, ⟨ ⟨ ⟨ qx;px′ ⟩ ⟩ ⟩ = 0, for some inverse temperature β, while in mechanical local equilibrium: ⟨ ⟨ ⟨ r[Ny](0) ⟩ ⟩ ⟩ → r(0,y), ⟨ ⟨ ⟨ p[Ny](0) ⟩ ⟩ ⟩ → p(0,y).

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Harmonic Chain: Thermal Equilibrium (classic case)

thermal equilibrium is conserved by the dynamics: for any t ≥ 0 ⟨ ⟨ ⟨ rx(t);rx′(t) ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ px(t);px′(t) ⟩ ⟩ ⟩ = β−1δx,x′, ⟨ ⟨ ⟨ qx(t);px′(t) ⟩ ⟩ ⟩ = 0,

Proof.

Thermal equilibrium is Fourier space is: ⟨ ⟨ ⟨ ˆ ψ(k,0)∗; ˆ ψ(k′,0) ⟩ ⟩ ⟩ = 2β−1δ(k − k′), ⟨ ⟨ ⟨ ˆ ψ(k,0); ˆ ψ(k′,0) ⟩ ⟩ ⟩ = 0.

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Harmonic Chain: Thermal Equilibrium (classic case)

thermal equilibrium is conserved by the dynamics: for any t ≥ 0 ⟨ ⟨ ⟨ rx(t);rx′(t) ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ px(t);px′(t) ⟩ ⟩ ⟩ = β−1δx,x′, ⟨ ⟨ ⟨ qx(t);px′(t) ⟩ ⟩ ⟩ = 0,

Proof.

Thermal equilibrium is Fourier space is: ⟨ ⟨ ⟨ ˆ ψ(k,0)∗; ˆ ψ(k′,0) ⟩ ⟩ ⟩ = 2β−1δ(k − k′), ⟨ ⟨ ⟨ ˆ ψ(k,0); ˆ ψ(k′,0) ⟩ ⟩ ⟩ = 0. Consequently ⟨ ⟨ ⟨ ˆ ψ(k,t)∗; ˆ ψ(k′,t) ⟩ ⟩ ⟩ = ei(ω(k)−ω(k′))t ⟨ ⟨ ⟨ ˆ ψ(k,0)∗; ˆ ψ(k′,0) ⟩ ⟩ ⟩ = 2β−1δ(k − k′) ⟨ ⟨ ⟨ ˆ ψ(k,t); ˆ ψ(k′,t) ⟩ ⟩ ⟩ = e−i(ω(k)+ω(k′))t ⟨ ⟨ ⟨ ˆ ψ(k,0); ˆ ψ(k′,0) ⟩ ⟩ ⟩ = 0.

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Harmonic Chain: Thermal Equilibrium implies Euler Equation limit

r[Ny](Nt) and p[Ny](Nt) converge weakly to the solution of the linear wave equation ∂tr (y,t) = ∂yp(y,t), ∂tp(y,t) = ∂yr (y,t). This is the Euler equation for this system since here τ(u,r) = r.

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Harmonic Chain: Thermal Equilibrium implies Euler Equation limit

r[Ny](Nt) and p[Ny](Nt) converge weakly to the solution of the linear wave equation ∂tr (y,t) = ∂yp(y,t), ∂tp(y,t) = ∂yr (y,t). This is the Euler equation for this system since here τ(u,r) = r. For the energy, because of the thermal equilibrium, for any t ≥ 0 : ⟨ ⟨ ⟨ E E Ex(t) ⟩ ⟩ ⟩ = β−1 + 1 2 (⟨ ⟨ ⟨ px(t) ⟩ ⟩ ⟩2 + ⟨ ⟨ ⟨ rx(t) ⟩ ⟩ ⟩2) ⟨ ⟨ ⟨ E E E[Ny](Nt) ⟩ ⟩ ⟩ → e(y,t) = β−1 + 1 2 (p2(y,t) + r2(y,t)), ∂te(y,t) = ∂y (p(y,t)r (y,t)).

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Quantum Harmonic Chain: Thermal Equilibrium

Initial density matrix ρβ, define ⟨ ⟨ ⟨ A ⟩ ⟩ ⟩ = tr(Aρβ)), ⟨ ⟨ ⟨ A;B ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ AB ⟩ ⟩ ⟩ − ⟨ ⟨ ⟨ A ⟩ ⟩ ⟩⟨ ⟨ ⟨ B ⟩ ⟩ ⟩ such that ⟨ ⟨ ⟨ rx(0);rx′(0) ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ px(0);px′(0) ⟩ ⟩ ⟩ = Cβ(x−x′), ⟨ ⟨ ⟨ qx;px′ ⟩ ⟩ ⟩ = i 2δ(x−x′) Cβ(x) = 1 N [β−1 + ∑

k≠0

e2πikx( ωk eβωk − 1 + ωk 2 )] (1)

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Quantum Harmonic Chain: Thermal Equilibrium

Initial density matrix ρβ, define ⟨ ⟨ ⟨ A ⟩ ⟩ ⟩ = tr(Aρβ)), ⟨ ⟨ ⟨ A;B ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ AB ⟩ ⟩ ⟩ − ⟨ ⟨ ⟨ A ⟩ ⟩ ⟩⟨ ⟨ ⟨ B ⟩ ⟩ ⟩ such that ⟨ ⟨ ⟨ rx(0);rx′(0) ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ px(0);px′(0) ⟩ ⟩ ⟩ = Cβ(x−x′), ⟨ ⟨ ⟨ qx;px′ ⟩ ⟩ ⟩ = i 2δ(x−x′) Cβ(x) = 1 N [β−1 + ∑

k≠0

e2πikx( ωk eβωk − 1 + ωk 2 )] (1) ⟨ ⟨ ⟨ r[Ny](0) ⟩ ⟩ ⟩ → r(0,y), ⟨ ⟨ ⟨ p[Ny](0) ⟩ ⟩ ⟩ → p(0,y). ⟨ ⟨ ⟨ E E E[Ny] ⟩ ⟩ ⟩ → e(y) = ¯ C(β) + 1 2 (p2(y) + r2(y)), ¯ C(β) = ∫

1 0 ω(k)(

1 eβω(k) − 1 + 1 2)dk ∼

β→0 β−1

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Quantum Harmonic Chain: Thermal Equilibrium implies Euler Equation limit

r[Ny](Nt) and p[Ny](Nt) converge weakly to the solution of the linear wave equation ∂tr (y,t) = ∂yp(y,t), ∂tp(y,t) = ∂yr (y,t). ⟨ ⟨ ⟨ E E E[Ny](Nt) ⟩ ⟩ ⟩ → e(y,t) = ¯ C(β) + 1 2 (p2(y,t) + r2(y,t)), ¯ C(β) = ∫

1 0 ω(k)(

1 eβω(k) − 1 + 1 2)dk ∼

β→0 β−1

∂te(y,t) = ∂y (p(y,t)r (y,t)).

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Harmonic Chain: Local Thermal Equilibrium is not conserved

The argument fails dramatically if the system is not in thermal equilibrium, even local thermal Gibbs ⟨ ⟨ ⟨ rx(0);rx′(0) ⟩ ⟩ ⟩ = ⟨ ⟨ ⟨ px(0);px′(0) ⟩ ⟩ ⟩ = β−1 ( x N )δx,x′, ⟨ ⟨ ⟨ qx(0);px′(0) ⟩ ⟩ ⟩ = 0 (2) is not conserved, and correlations between px(t) and rx(t) build up in time. No autonomous macroscopic equation for the energy! There are infinite many conservation laws.

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SLIDE 42

Wigner distribution

ξ ∈ R, k ∈ [0,1], ̂ WN(ξ,k,t) ∶= 2 N ⟨ ⟨ ⟨ ˆ ψ∗ (Nt,k − ξ 2N ) ˆ ψ (Nt,k + ξ 2N ) ⟩ ⟩ ⟩ WN(y,k,t) = ∫ ̂ WN(t,η,k)e−i2πξy dη, y ∈ R,

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slide-43
SLIDE 43

Wigner distribution

ξ ∈ R, k ∈ [0,1], ̂ WN(ξ,k,t) ∶= 2 N ⟨ ⟨ ⟨ ˆ ψ∗ (Nt,k − ξ 2N ) ˆ ψ (Nt,k + ξ 2N ) ⟩ ⟩ ⟩ WN(y,k,t) = ∫ ̂ WN(t,η,k)e−i2πξy dη, y ∈ R, In the limit it decompose in a thermal and a mechanical part: lim

N→∞

̂ WN(ξ,k,t) = ̂ Wth(ξ,k,t) + ̂ Wm(ξ,t) δ0(dk) (3) The mechanical part ̂ Wm(ξ,t) is the Fourier transform of the mechanical energy ̂ Wm(ξ,t) = ∫ 1 2 (p2(y,t) + r2(y,t))ei2πξy dy,

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slide-44
SLIDE 44

Wigner distribution

For the thermal Wigner distribution it holds the transport equation: ∂tWth(y,k,t) + ω′(k) 2π ∂yWth(y,k,t) = 0.

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slide-45
SLIDE 45

Wigner distribution

For the thermal Wigner distribution it holds the transport equation: ∂tWth(y,k,t) + ω′(k) 2π ∂yWth(y,k,t) = 0. in fact for k ≠ 0 ̂ WN(ξ,k,t) ∶= ei[ω(k− ξ

2N )−ω(k+ ξ 2N )]Nt ̂

WN(ξ,k,0) ∼

N→∞ e−iω′(k)ξt ̂

Wth(ξ,k,0)

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slide-46
SLIDE 46

Wigner distribution

For the thermal Wigner distribution it holds the transport equation: ∂tWth(y,k,t) + ω′(k) 2π ∂yWth(y,k,t) = 0. in fact for k ≠ 0 ̂ WN(ξ,k,t) ∶= ei[ω(k− ξ

2N )−ω(k+ ξ 2N )]Nt ̂

WN(ξ,k,0) ∼

N→∞ e−iω′(k)ξt ̂

Wth(ξ,k,0) W (t,y,k) = W (0,y − ω′(k) 2π t,k) Phonon of wave number k moves freely with velocity ω′(k)

2π .

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slide-47
SLIDE 47

Wigner distribution

Consequently the thermal energy ˜ e(y,t) (i.e. temperature) evolves non autonomously following the equation ∂t˜ e(y,t) + ∂yJ(y,t) = 0, J(y,t) = ∫ ω′(k)Wth(y,k,t) dk. We say that the system is in local equilibrium if Wth(y,k) = β−1(y) constant in k. Starting in thermal equilibrium means Wth(y,k,0) = β−1 and trivially Wth(y,k,t) = β−1 for any t > 0. But starting with local equilibrium, i.e. W (y,k,0) = β−1(y) constant in k, we have a non autonomous evolution of ˜ e(y,t).

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slide-48
SLIDE 48

Harmonic Chain with Random Masses

The problem with the harmonic chain is that thermal waves of wavenumber k move with speed ω′(k), if they are not uniformed distributed (i.e. the system is not in thermal equilibrium), the temperature profile will not remain constant, as it should be following the Euler equations.

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slide-49
SLIDE 49

Harmonic Chain with Random Masses

The problem with the harmonic chain is that thermal waves of wavenumber k move with speed ω′(k), if they are not uniformed distributed (i.e. the system is not in thermal equilibrium), the temperature profile will not remain constant, as it should be following the Euler equations. If the masses are random, the thermal modes remains localized (frozen), by Anderson localization. This allows to close the energy equation, without local equilibrium.

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slide-50
SLIDE 50

Harmonic Chain with Random Masses

(F. Huveneers, C. Bernardin, S.Olla, 2017) {mx} i.i.d. with absolutely continuous distribution, 0 < m− ≤ mx ≤ m+, m = E(mx). mx ˙ qx(t) = px(t), ˙ px(t) = ∆qx(t), x = 1,...,N with q0 = q1 and qN+1 = qN as boundary conditions.

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slide-51
SLIDE 51

Gibbs States, Local Gibbs States

The Gibbs states are characterized by three parameters: β > 0 and p,r ∈ R. Its probability density writes

N

x=1

e

− βmx

2 ( px mx − p m) 2

− β

2 (rx−r)2

Z(β,p,r,mx) .

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slide-52
SLIDE 52

Gibbs States, Local Gibbs States

The Gibbs states are characterized by three parameters: β > 0 and p,r ∈ R. Its probability density writes

N

x=1

e

− βmx

2 ( px mx − p m) 2

− β

2 (rx−r)2

Z(β,p,r,mx) . We start with a local Gibbs state:

N

x=1

e

− β(x/N)mx

2

( px

mx − p(x/N) m

)

2

− β(x/N)

2

(rx−r(x/N))2

Z(β(x/N),p(x/N),r(x/N),mx) .

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slide-53
SLIDE 53

Harmonic Chain with Random Masses: hydrodynamic limit

Almost surely with respect to {mx}: < r[Ny](Nt) >,< p[Ny](Nt) >,< E E E[Ny](Nt) > ⇀ (r(y,t),p(y,t),e(y,t)) ∂tr(t,y) = 1 m∂yp(t,y) ∂tp(t,y) = ∂yr(t,y) ∂te(t,y) = 1 m∂y (r(t,y)p(t,y)) with initial conditions: r(y,0) = r(y), p(y,0) = p(y), e(y,0) = 1 β(y)+p2(y) 2m +r2(y) 2 .

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slide-54
SLIDE 54

Random Masses: Localization of Thermal Modes

Equation of motion can be written as ¨ rx = −(∇∗M−1∇r)x (1 ≤ x ≤ N−1), ¨ px = (∆M−1p)x (1 ≤ x ≤ N), where Mx,x′ = δx,x′mx.

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slide-55
SLIDE 55

Random Masses: Localization of Thermal Modes

Equation of motion can be written as ¨ rx = −(∇∗M−1∇r)x (1 ≤ x ≤ N−1), ¨ px = (∆M−1p)x (1 ≤ x ≤ N), where Mx,x′ = δx,x′mx. M−1/2(−∆)M1/2ϕk = ω2

k ϕk,

k = 0,...,N − 1. ψk = M−1/2ϕk, M−1∆ψk = ω2

kψk

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slide-56
SLIDE 56

Random Masses: Localization of Thermal Modes

Equation of motion can be written as ¨ rx = −(∇∗M−1∇r)x (1 ≤ x ≤ N−1), ¨ px = (∆M−1p)x (1 ≤ x ≤ N), where Mx,x′ = δx,x′mx. M−1/2(−∆)M1/2ϕk = ω2

k ϕk,

k = 0,...,N − 1. ψk = M−1/2ϕk, M−1∆ψk = ω2

kψk

r(t) =

N−1

k=1

(⟨∇ψk,r(0)⟩ ωk cosωkt + ⟨ψk,p(0)⟩sinωkt)∇ψk ωk , p(t) =

N−1

k=0

(⟨ψk,p(0)⟩cosωkt − ⟨∇ψk,r(0)⟩ ωk sinωkt)Mψk.

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slide-57
SLIDE 57

Localization of Thermal Modes

Localization length ξk diverges with N: ξ−1

k

∼ ω2

k ∼ ( k

N )

2

,

  • nly the modes k >

√ N are localized.

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slide-58
SLIDE 58

Localization of Thermal Modes

Localization length ξk diverges with N: ξ−1

k

∼ ω2

k ∼ ( k

N )

2

,

  • nly the modes k >

√ N are localized. More precisely: for 0 < α < 1

2

E⎛ ⎝

N−1

k=N1−α

∣ψk

x ψk x′∣⎞

⎠ ≤ Ce−cN−2α∣x−x′∣. This estimate is enough to prove that thermal modes remains localized and do not move macroscopically.

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slide-59
SLIDE 59

Random masses: Larger time scales

Assume for simplicity that we are in a mechanical equilibrium: ⟨ ⟨ ⟨ rx(0) ⟩ ⟩ ⟩ = 0, ⟨ ⟨ ⟨ px(0) ⟩ ⟩ ⟩ = 0, (only thermal energy present) but not in thermal equilibrium, then, for any α ≥ 1 < E E E[Ny](Nαt) > →

N to∞ e(0,y) = ¯

C(β(y)) NO evolution for the temperature profile at any scale!

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slide-60
SLIDE 60

Random masses: Larger time scales

Assume for simplicity that we are in a mechanical equilibrium: ⟨ ⟨ ⟨ rx(0) ⟩ ⟩ ⟩ = 0, ⟨ ⟨ ⟨ px(0) ⟩ ⟩ ⟩ = 0, (only thermal energy present) but not in thermal equilibrium, then, for any α ≥ 1 < E E E[Ny](Nαt) > →

N to∞ e(0,y) = ¯

C(β(y)) NO evolution for the temperature profile at any scale! In particular, for α = 2 (diffusive scaling), thermal diffusivity is null.

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slide-61
SLIDE 61

Open questions for the quantum case

▸ In order to deal with the anharmonic interaction, in the

classical case, conservative noise is added to obtain ergodicity

  • f the infinite dynamics (unique characterization of the

translational invariant stationary states) ( cf B. Nachtergaele, and H-T Yau, CMP 2003). How to add conservative noise in the quantum dynamics in

  • rder to obtain similar result?
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slide-62
SLIDE 62

Open questions for the quantum case

▸ In order to deal with the anharmonic interaction, in the

classical case, conservative noise is added to obtain ergodicity

  • f the infinite dynamics (unique characterization of the

translational invariant stationary states) ( cf B. Nachtergaele, and H-T Yau, CMP 2003). How to add conservative noise in the quantum dynamics in

  • rder to obtain similar result?

▸ Boundary tension? More generally boundary conditions,

thermostat etc.

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slide-63
SLIDE 63

entropy evolution

∂tr = ∂xp ∂tp = ∂xτ ∂te = ∂x(τp) p(t,0) = 0, τ(r(1,t),u(1,t)) = τ(t) U = e − p2/2, β = ∂S

∂U , τ = − 1 β ∂S ∂r

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slide-64
SLIDE 64

entropy evolution

∂tr = ∂xp ∂tp = ∂xτ ∂te = ∂x(τp) p(t,0) = 0, τ(r(1,t),u(1,t)) = τ(t) U = e − p2/2, β = ∂S

∂U , τ = − 1 β ∂S ∂r

For smooth solutions: d dt S(u(y,t),r(y,t)) = β (∂te − p∂tp) − βτ∂tr = β (∂x(τp) − p∂xτ − τ∂xp) = 0 The evolution is isoentropic in the smooth regime.

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slide-65
SLIDE 65

Shocks, contact discontinuities, weak solutions, entropy solutions

Even starting with initial smooth profiles, hyperbolic non-linear systems develops discontinuities:

▸ shocks: discontinuities in the tension profile,

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slide-66
SLIDE 66

Shocks, contact discontinuities, weak solutions, entropy solutions

Even starting with initial smooth profiles, hyperbolic non-linear systems develops discontinuities:

▸ shocks: discontinuities in the tension profile, ▸ contact discontinuities: discontinuities in the entropy profile.

When this happens we have to consider weak solution, that typically are not unique.

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slide-67
SLIDE 67

Shocks, contact discontinuities, weak solutions, entropy solutions

Even starting with initial smooth profiles, hyperbolic non-linear systems develops discontinuities:

▸ shocks: discontinuities in the tension profile, ▸ contact discontinuities: discontinuities in the entropy profile.

When this happens we have to consider weak solution, that typically are not unique. In order to select the right physical solutions, various properties (maybe equivalent) have been introduced:

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slide-68
SLIDE 68

Shocks, contact discontinuities, weak solutions, entropy solutions

Even starting with initial smooth profiles, hyperbolic non-linear systems develops discontinuities:

▸ shocks: discontinuities in the tension profile, ▸ contact discontinuities: discontinuities in the entropy profile.

When this happens we have to consider weak solution, that typically are not unique. In order to select the right physical solutions, various properties (maybe equivalent) have been introduced:

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slide-69
SLIDE 69

Shocks, contact discontinuities, weak solutions, entropy solutions

Even starting with initial smooth profiles, hyperbolic non-linear systems develops discontinuities:

▸ shocks: discontinuities in the tension profile, ▸ contact discontinuities: discontinuities in the entropy profile.

When this happens we have to consider weak solution, that typically are not unique. In order to select the right physical solutions, various properties (maybe equivalent) have been introduced:

▸ entropy solutions

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slide-70
SLIDE 70

Shocks, contact discontinuities, weak solutions, entropy solutions

Even starting with initial smooth profiles, hyperbolic non-linear systems develops discontinuities:

▸ shocks: discontinuities in the tension profile, ▸ contact discontinuities: discontinuities in the entropy profile.

When this happens we have to consider weak solution, that typically are not unique. In order to select the right physical solutions, various properties (maybe equivalent) have been introduced:

▸ entropy solutions ▸ viscosity solutions

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slide-71
SLIDE 71

weak solutions

Consider a hyperbolic system of conservation laws vt + f (v)x = 0, a weak solution v(t,y) on an open set Ω ⊂ R2 satisfies, for any function φ(t,y) ∈ C1 with compact support in Ω ∬Ω [φtv + φyf (v)]dy dt = 0 No continuity assumption is made on v.

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slide-72
SLIDE 72

weak solutions

Consider a hyperbolic system of conservation laws vt + f (v)x = 0, a weak solution v(t,y) on an open set Ω ⊂ R2 satisfies, for any function φ(t,y) ∈ C1 with compact support in Ω ∬Ω [φtv + φyf (v)]dy dt = 0 No continuity assumption is made on v. In the Euler case, v = (r,p,e), u = e − p2/2 and f (v) = − ⎛ ⎜ ⎝ p τ(u,r) pτ(u,r) ⎞ ⎟ ⎠ Strictly Hyperbolic System: the Jacobian matrix Df has real distinct eigenvalues.

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slide-73
SLIDE 73

weak solutions: Cauchy initial problem

A weak solution of vt + f (v)x = 0, v(0,y) = v0(y), is a weak solution of the Cauchy initial data problem if t ∈ [0,T] → v(t,⋅) is continuous in L1

loc.

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slide-74
SLIDE 74

weak solutions: Cauchy initial problem

A weak solution of vt + f (v)x = 0, v(0,y) = v0(y), is a weak solution of the Cauchy initial data problem if t ∈ [0,T] → v(t,⋅) is continuous in L1

loc.

unfortunately it may not be unique! Existence proved only for v0 of bounded variation (Glimm,....).

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slide-75
SLIDE 75

Entropic weak solutions

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn

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slide-76
SLIDE 76

Entropic weak solutions

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn A C1 function η ∶ Rn → R is an entropy function with entropy flux q ∶ Rn → R, if Dη(v) ⋅ Df (v) = Dq(v) that implies for smooth solutions: η(v)t + q(v)x = 0.

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slide-77
SLIDE 77

Entropic weak solutions

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn A C1 function η ∶ Rn → R is an entropy function with entropy flux q ∶ Rn → R, if Dη(v) ⋅ Df (v) = Dq(v) that implies for smooth solutions: η(v)t + q(v)x = 0.

▸ n = 1: any convex non-linear η is an entropy function,

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slide-78
SLIDE 78

Entropic weak solutions

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn A C1 function η ∶ Rn → R is an entropy function with entropy flux q ∶ Rn → R, if Dη(v) ⋅ Df (v) = Dq(v) that implies for smooth solutions: η(v)t + q(v)x = 0.

▸ n = 1: any convex non-linear η is an entropy function, ▸ n ≥ 3: ? It may nont exists

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slide-79
SLIDE 79

Entropic weak solutions

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn A C1 function η ∶ Rn → R is an entropy function with entropy flux q ∶ Rn → R, if Dη(v) ⋅ Df (v) = Dq(v) that implies for smooth solutions: η(v)t + q(v)x = 0.

▸ n = 1: any convex non-linear η is an entropy function, ▸ n ≥ 3: ? It may nont exists ▸ For the Euler System: the thermodynamic entropy

η(v) = S(e − p2/2,r) is an entropy function.

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slide-80
SLIDE 80

Entropic weak solution

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn An weak solution is entropy-admissible if η(v)t + q(v)x ≤ 0 as distribution, for any entropy pair (η,q).

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slide-81
SLIDE 81

Entropic weak solution

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn An weak solution is entropy-admissible if η(v)t + q(v)x ≤ 0 as distribution, for any entropy pair (η,q). This implies that total entropy ∫ η(v(t,y))dy increase in time (with no b.c. here).

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slide-82
SLIDE 82

Entropic weak solution

vt + f (v)x = 0, v(0,y) = v0(y), v(t,y) ∈ Rn An weak solution is entropy-admissible if η(v)t + q(v)x ≤ 0 as distribution, for any entropy pair (η,q). This implies that total entropy ∫ η(v(t,y))dy increase in time (with no b.c. here). Existence is proven only under bounded variation initial conditions. The conjecture is that entropy-admissible solutions are unique.

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slide-83
SLIDE 83

Vanishing viscosity solutions

t + f (vε)x = εvε xx,

  • r more general

t + f (vε)x = εΛ(vε),

where Λ is a second order differential operator (eventually non-linear).

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slide-84
SLIDE 84

Vanishing viscosity solutions

t + f (vε)x = εvε xx,

  • r more general

t + f (vε)x = εΛ(vε),

where Λ is a second order differential operator (eventually non-linear). If vε converges in L1

loc as ε → 0+, this is called a vanishing viscosity

solution.

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slide-85
SLIDE 85

Vanishing viscosity solutions

t + f (vε)x = εvε xx,

  • r more general

t + f (vε)x = εΛ(vε),

where Λ is a second order differential operator (eventually non-linear). If vε converges in L1

loc as ε → 0+, this is called a vanishing viscosity

solution. Bianchini-Bressan (AoM, 2005): if initial data are of small BV, limit exists unique and is BV and is an entropy solution, (for linear viscosity).

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slide-86
SLIDE 86

Isothermal Dynamics

▸ J. Fritz, Microscopic theory of isothermal elasticity, ARMA

2011, infinite volume

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slide-87
SLIDE 87

Isothermal Dynamics

▸ J. Fritz, Microscopic theory of isothermal elasticity, ARMA

2011, infinite volume

▸ S. Marchesani, S. Olla, Nonlinearity 2018, boundary

conditions. The system is in contact with a heat bath that keeps it at a constant temperature β−1. Energy is not conserved anymore. Macroscopically we have a p-system: ∂tr(t,y) = ∂yp(t,y) ∂tp(t,y) = ∂yτ[β,r(t,y)]

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slide-88
SLIDE 88

MIcroscopic isothermal dynamics

⎧ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎨ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎩ dr1 = Np1dt + NσN (V ′(r2) − V ′(r1)) dt − √ 2β−1NσNd ̃ w1 dri = N(pi − pi−1)dt + NσN (V ′(ri+1) + V ′(ri−1) − 2V ′(ri )) dt + √ 2β−1NσN(d ̃ wi−1 − d ̃ wi ) drN = N(pN − pN−1)dt + NσN (V ′(rN−1) − V ′(rN)) dt + √ 2β−1Nσd ̃ wN−1 dp1 = N(V ′(r2) − V ′(r1))dt + NσN (p2 − p1) dt − √ 2β−1NσNdw1 dpi = N(V ′(ri+1) − V ′(ri ))dt + NσN (pi+1 + pi−1 − 2pi ) dt + √ 2β−1NσN(dwi−1 − dwi ) dpN = N(¯ τ(t) − V ′(rN))dt + NσN (pN−1 − pN) dt + √ 2β−1NσNdwN−1, ,

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hyperbolic limits

slide-89
SLIDE 89

MIcroscopic isothermal dynamics

⎧ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎨ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎪ ⎩ dr1 = Np1dt + NσN (V ′(r2) − V ′(r1)) dt − √ 2β−1NσNd ̃ w1 dri = N(pi − pi−1)dt + NσN (V ′(ri+1) + V ′(ri−1) − 2V ′(ri )) dt + √ 2β−1NσN(d ̃ wi−1 − d ̃ wi ) drN = N(pN − pN−1)dt + NσN (V ′(rN−1) − V ′(rN)) dt + √ 2β−1Nσd ̃ wN−1 dp1 = N(V ′(r2) − V ′(r1))dt + NσN (p2 − p1) dt − √ 2β−1NσNdw1 dpi = N(V ′(ri+1) − V ′(ri ))dt + NσN (pi+1 + pi−1 − 2pi ) dt + √ 2β−1NσN(dwi−1 − dwi ) dpN = N(¯ τ(t) − V ′(rN))dt + NσN (pN−1 − pN) dt + √ 2β−1NσNdwN−1, ,

lim

N→+∞

σN N = lim

N→∞

N σN2 = 0.

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hyperbolic limits

slide-90
SLIDE 90

Isothermal dynamics, generator

τ(t) N

∶= NL¯

τ(t) N

+ NσN(SN + ˜ SN). L¯

τ(t) N

=

N

i=1

(pi−pi−1)∂ri+

N−1

i=1

(V ′(ri+1) − V ′(ri))∂pi+(¯ τ(t)−V ′(rN))∂pN,

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hyperbolic limits

slide-91
SLIDE 91

Isothermal dynamics, generator

τ(t) N

∶= NL¯

τ(t) N

+ NσN(SN + ˜ SN). L¯

τ(t) N

=

N

i=1

(pi−pi−1)∂ri+

N−1

i=1

(V ′(ri+1) − V ′(ri))∂pi+(¯ τ(t)−V ′(rN))∂pN, SN ∶= −

N−1

i=1

D∗

i Di,

˜ SN ∶= −

N−1

i=1

˜ D∗

i ˜

Di, Di ∶= ∂ ∂pi+1 − ∂ ∂pi , D∗

i ∶= pi+1 − pi − β−1Di

˜ Di ∶= ∂ ∂ri+1 − ∂ ∂ri , ˜ D∗

i ∶= V ′(ri+1) − V ′(ri) − β−1 ˜

Di.

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hyperbolic limits

slide-92
SLIDE 92

Initial distribution

The density f N

t

with respect to µN = µN

β,0,0 solves the Fokker-Plank

equation ∂f N

t

∂t = (G¯

τ(t) N

)

f N

t .

Here (G¯

τ(t) N

)

= −NL¯

τ(t) N

+ N¯ τ(t)pN + Nσ(SN + ˜ SN) is the adjoint

  • f G¯

τ(t) N

with respect to µN.

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hyperbolic limits

slide-93
SLIDE 93

Initial distribution

The density f N

t

with respect to µN = µN

β,0,0 solves the Fokker-Plank

equation ∂f N

t

∂t = (G¯

τ(t) N

)

f N

t .

Here (G¯

τ(t) N

)

= −NL¯

τ(t) N

+ N¯ τ(t)pN + Nσ(SN + ˜ SN) is the adjoint

  • f G¯

τ(t) N

with respect to µN. relative entropy HN(f N

t ) ∶= ∫R2N f N t log f N t dµN

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hyperbolic limits

slide-94
SLIDE 94

Initial distribution

The density f N

t

with respect to µN = µN

β,0,0 solves the Fokker-Plank

equation ∂f N

t

∂t = (G¯

τ(t) N

)

f N

t .

Here (G¯

τ(t) N

)

= −NL¯

τ(t) N

+ N¯ τ(t)pN + Nσ(SN + ˜ SN) is the adjoint

  • f G¯

τ(t) N

with respect to µN. relative entropy HN(f N

t ) ∶= ∫R2N f N t log f N t dµN

assume or the initial distribution HN(f N

0 ) ≤ CN.

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hyperbolic limits

slide-95
SLIDE 95

Limite Hydrodynamique

1 N ∑

x

G(x/N)(rx(t) px(t)) →

N→∞ ∫ 1 0 G(y)(r(y,t)

p(y,t)) dy L2-valued weak solution of ∂tr(t,y) = ∂yp(t,y) ∂tp(t,y) = ∂yτβ[r(t,y)] p(t,0) = 0, τ(r(t,1)) = ¯ τ(t), in the sense

1 0 (r(t,x)∂tϕ(t,x) − p(t,x)∂xϕ(t,x))dx dt = 0

1 0 (p(t,x)∂tψ(t,x) − τβ(r(t,x))∂xψ(t,x))dx dt = 0

for all functions ϕ,ψ with compact support on R+ ∖ {0} × (0,1). NO information on initial and boundary conditions, no entropy condition.

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hyperbolic limits

slide-96
SLIDE 96

Vanishing viscosity

The heat bath interaction in the dynamics plays the role of a microscopic viscosity, vanishing in the macroscopic limit.

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hyperbolic limits

slide-97
SLIDE 97

Vanishing viscosity

The heat bath interaction in the dynamics plays the role of a microscopic viscosity, vanishing in the macroscopic limit. The corresponding viscous equations would be: ⎧ ⎪ ⎪ ⎨ ⎪ ⎪ ⎩ ∂trε(t,x) − ∂xpε(t,x) = ε∂xxτβ(rε(t,x)) x ∈ (0,1) ∂tpε(t,x) − ∂xτβ(rε(t,x)) = ε∂xxpε(t,x), with boundary conditions pε(t,0) = 0, τ(rε(t,1)) = ¯ τ(t), ∂xpε(t,1) = 0, ∂xrε(t,0) = 0,

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hyperbolic limits

slide-98
SLIDE 98

Vanishing viscosity

The heat bath interaction in the dynamics plays the role of a microscopic viscosity, vanishing in the macroscopic limit. The corresponding viscous equations would be: ⎧ ⎪ ⎪ ⎨ ⎪ ⎪ ⎩ ∂trε(t,x) − ∂xpε(t,x) = ε∂xxτβ(rε(t,x)) x ∈ (0,1) ∂tpε(t,x) − ∂xτβ(rε(t,x)) = ε∂xxpε(t,x), with boundary conditions pε(t,0) = 0, τ(rε(t,1)) = ¯ τ(t), ∂xpε(t,1) = 0, ∂xrε(t,0) = 0, Note the non-linear viscosity term.

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hyperbolic limits

slide-99
SLIDE 99

Vanishing viscosity

The heat bath interaction in the dynamics plays the role of a microscopic viscosity, vanishing in the macroscopic limit. The corresponding viscous equations would be: ⎧ ⎪ ⎪ ⎨ ⎪ ⎪ ⎩ ∂trε(t,x) − ∂xpε(t,x) = ε∂xxτβ(rε(t,x)) x ∈ (0,1) ∂tpε(t,x) − ∂xτβ(rε(t,x)) = ε∂xxpε(t,x), with boundary conditions pε(t,0) = 0, τ(rε(t,1)) = ¯ τ(t), ∂xpε(t,1) = 0, ∂xrε(t,0) = 0, Note the non-linear viscosity term. As ε → 0 boundary layers may appear.

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hyperbolic limits

slide-100
SLIDE 100

The p-system

It is usually difficult to control bounds in the vanishing viscosity ε → 0, Bressan-Bianchini can do it for the BV if viscosity is taken linear. For the p-system with no boundaries ∂tr(t,y) = ∂yp(t,y) ∂tp(t,y) = ∂yτβ[r(t,y)] can be proven existence of L∞ weak solutions (Di Perna), and L2 valued solutions (Schearer, Serre-Shearer).

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hyperbolic limits

slide-101
SLIDE 101

The p-system

It is usually difficult to control bounds in the vanishing viscosity ε → 0, Bressan-Bianchini can do it for the BV if viscosity is taken linear. For the p-system with no boundaries ∂tr(t,y) = ∂yp(t,y) ∂tp(t,y) = ∂yτβ[r(t,y)] can be proven existence of L∞ weak solutions (Di Perna), and L2 valued solutions (Schearer, Serre-Shearer). When boundaries are present, it is less clear how to define weak solutions that are not of BV.

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slide-102
SLIDE 102

Viscosity solutions with boundary values

One proposal would be to take L2 limits as ε → 0 of ⎧ ⎪ ⎪ ⎨ ⎪ ⎪ ⎩ ∂trε(t,x) − ∂xpε(t,x) = ε∂xxτβ(rε(t,x)) x ∈ (0,1) ∂tpε(t,x) − ∂xτβ(rε(t,x)) = ε∂xxpε(t,x), pε(t,0) = 0, τ(rε(t,1)) = ¯ τ(t), ∂xpε(t,1) = 0, ∂xrε(t,0) = 0,

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hyperbolic limits

slide-103
SLIDE 103

Viscosity solutions with boundary values

One proposal would be to take L2 limits as ε → 0 of ⎧ ⎪ ⎪ ⎨ ⎪ ⎪ ⎩ ∂trε(t,x) − ∂xpε(t,x) = ε∂xxτβ(rε(t,x)) x ∈ (0,1) ∂tpε(t,x) − ∂xτβ(rε(t,x)) = ε∂xxpε(t,x), pε(t,0) = 0, τ(rε(t,1)) = ¯ τ(t), ∂xpε(t,1) = 0, ∂xrε(t,0) = 0, The non-linearity in the viscosity gives the right entropy production.

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hyperbolic limits

slide-104
SLIDE 104

Entropy production and Clausius inequality

Let vε(t,y) = rε(t,y),pε(t,y). Free energy at time t: F(vε(t)) = ∫

1 0 [pε(t,y)2

2 + Fβ(rε(t,y))] dy, ∂rFβ(r) = τβ(r),

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hyperbolic limits

slide-105
SLIDE 105

Entropy production and Clausius inequality

Let vε(t,y) = rε(t,y),pε(t,y). Free energy at time t: F(vε(t)) = ∫

1 0 [pε(t,y)2

2 + Fβ(rε(t,y))] dy, ∂rFβ(r) = τβ(r), F(vε(t))−F(v(0)) = W (t) − ε∫

t 0 ds ∫ 1 0 dy [(∂yτβ(rε(s,y))) 2 + (∂xpε(s,y))2]

≥ W (t) where W (t) is the work done by the boundary force τ(t). So we expect that this particular limit generates the right entropy solutions.

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hyperbolic limits

slide-106
SLIDE 106

Various remarks

▸ For scalar equations (one conserved quantity) the theory of

boundary conditions is much simpler, and boundary layers do not depend on the detalis of the approximation (Bardos-Leroux-Nedelec, F. Otto), and there is a good definition of boundary entropy condition.

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hyperbolic limits

slide-107
SLIDE 107

Various remarks

▸ For scalar equations (one conserved quantity) the theory of

boundary conditions is much simpler, and boundary layers do not depend on the detalis of the approximation (Bardos-Leroux-Nedelec, F. Otto), and there is a good definition of boundary entropy condition.

▸ Hydrodynamic limit for one conserved quantity (Burgers

equation) with boundary conditions have been proven by Bahadoran (from ASEP).

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hyperbolic limits

slide-108
SLIDE 108

Various remarks

▸ For scalar equations (one conserved quantity) the theory of

boundary conditions is much simpler, and boundary layers do not depend on the detalis of the approximation (Bardos-Leroux-Nedelec, F. Otto), and there is a good definition of boundary entropy condition.

▸ Hydrodynamic limit for one conserved quantity (Burgers

equation) with boundary conditions have been proven by Bahadoran (from ASEP).

▸ There exists extention to systems of the boundary entropy

condition (Chen-Frid), but with BV solutions.

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hyperbolic limits

slide-109
SLIDE 109

Compensated compactness

▸ The Fritz’s approach that we use is based on a stochastic

version of the compensated compactness lemma of Tartar-Murat. This was used by Di Perna to prove existence

  • f vanishing viscosity limits in p-systems.
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hyperbolic limits

slide-110
SLIDE 110

Compensated compactness

▸ The Fritz’s approach that we use is based on a stochastic

version of the compensated compactness lemma of Tartar-Murat. This was used by Di Perna to prove existence

  • f vanishing viscosity limits in p-systems.

▸ This is a trick to prove that weak limit of viscous solutions

vve are actually strong limit, which is also the main problem in hydrodynamic limits from microscopic dynamics.

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hyperbolic limits

slide-111
SLIDE 111

Compensated compactness

▸ The Fritz’s approach that we use is based on a stochastic

version of the compensated compactness lemma of Tartar-Murat. This was used by Di Perna to prove existence

  • f vanishing viscosity limits in p-systems.

▸ This is a trick to prove that weak limit of viscous solutions

vve are actually strong limit, which is also the main problem in hydrodynamic limits from microscopic dynamics.

▸ Unfortunately the trick works only when one has many (at

least two) entropy pairs ((η1,q1), (η2,q2)). This restrict the trick to 2x2 systems of conservation law, cannot be used for the Euler equation 3x3, where we know only the thermodynamic entropy as mathematical entropy.

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slide-112
SLIDE 112

Compensated compactness

ηj(vε)t + qj(vε)x ∈ compact set inH−1, j = 1,2 then η1(vε)q2(εε) − η2(vε)q1(vε) converge weakly in L∞, and this is enough to establish the strong convergence of vε.

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hyperbolic limits