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Non-equilibrium thermodynamics

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second law of thermodynamics
law of physics stating that systems spontaneously evolve towards states of higher entropy
zero-point energy
lowest possible energy of a quantum system or field
dissipative system
thermodynamically open system which is operating out of, and often far from, thermodynamic equilibrium in an environment with which it exchanges energy and matter
autopoiesis
thumb|3D representation of a living cell during the process of mitosis, example of an autopoietic system
arrow of time
one-way direction, or asymmetry, of time
dissipation
In thermodynamics, dissipation is the result of an irreversible process that affects a thermodynamic system. In a dissipative process, energy (internal, bulk flow kinetic, or system potential) transforms from an initial form to a final form, where the capacity of the final form to do thermodynamic work is less than that of the initial form. For example, transfer of energy as heat is dissipative because it is a transfer of energy other than by thermodynamic work or by transfer of matter, and spreads previously concentrated energy. Following the second law of thermodynamics, in conduction and ra
Belousov–Zhabotinsky reaction
one of a class of reactions that serve as a classical example of non-equilibrium thermodynamics, resulting in the establishment of a nonlinear chemical oscillator
non-equilibrium thermodynamics
branch of thermodynamics
time crystal
quantum system whose ground state is one in which the particles are in repetitive motion
thermophoresis
thumb|Dust deposition by thermophoresis. Thermophoresis (also thermomigration, thermodiffusion, the Soret effect, or the Ludwig–Soret effect) is a phenomenon observed in mixtures of mobile particles where the different particle types exhibit different responses to the force of a temperature gradient. This phenomenon tends to move light molecules to hot regions and heavy molecules to cold regions. The term thermophoresis most often applies to aerosol mixtures whose mean free path \lambda is comparable to its characteristic length scale L, but may also commonly refer to the phenomenon in all pha
Onsager reciprocal relations
equality of certain ratios between flows and forces in thermodynamic systems out of equilibrium
H-theorem
In classical statistical mechanics, the ' H-theorem', introduced by Ludwig Boltzmann in 1872, describes the tendency of the quantity H (defined below) to decrease in a nearly-ideal gas of molecules. As this quantity H was meant to represent the entropy of thermodynamics, the H-theorem was an early demonstration of the power of statistical mechanics as it claimed to derive the second law of thermodynamics—a statement about fundamentally irreversible processes—from reversible microscopic mechanics. It is thought to prove the second law of thermodynamics, albeit under the assumption of low-entrop
Briggs–Rauscher reaction
oscillating chemical reaction of white, yellow and blue
quantum thermodynamics
study of quantum-mechanical thermodynamic systems and processes
fluctuation-dissipation theorem
theorem
Loschmidt's paradox
in physics, the apparent contradiction that time-irreversible macrophysics arises from time-symmetric microphysics
chemical clock
reaction that changes observably after a time
BBGKY hierarchy
set of equations describing the dynamics of a system of many interacting particles
detailed balance
term
electrokinetic phenomena
family of several different effects that occur in heterogeneous fluids, or in porous bodies filled with fluid, or in a fast flow over a flat surface
Brusselator
thumb|right|350px|Top: The Brusselator in the unstable regime (A=1, B=3): The system approaches a limit cycle Bottom: The Brusselator in a stable regime with A=1 and B=1.7: For B2 the system is stable and approaches a fixed point.
Vlasov equation
partial differential equation describing the time evolution of plasma
fluctuation theorem
theorem
Exergy efficiency
measure of performance of heat engines
chemical oscillator
non-equilibrium chemical reaction in which concentrations of components oscillate
Green–Kubo relations
equation relating transport coefficients to correlation functions
Oregonator
thumb|alt=Limit cycle oscillation of Oregonator|Limit cycle oscillation of Oregonator The Oregonator is a theoretical model for a type of autocatalytic reaction. The Oregonator is the simplest realistic model of the chemical dynamics of the oscillatory Belousov–Zhabotinsky reaction. It was created by Richard Field and Richard M. Noyes at the University of Oregon. It is a portmanteau of Oregon and oscillator.
Sedimentation potential
occurs when dispersed particles move under the influence of either gravity or centrifugation in a medium
Jarzynski equality
equation in statistical mechanics that relates free energy differences between two states and the irreversible work along an ensemble of trajectories joining the same states