Critical point (thermodynamics)In thermodynamics, a critical point (or critical state) is the end point of a phase equilibrium curve. One example is the liquid–vapor critical point, the end point of the pressure–temperature curve that designates conditions under which a liquid and its vapor can coexist. At higher temperatures, the gas comes into a supercritical phase, and so cannot be liquefied by pressure alone.
Theorem of corresponding statesThermodynamicsThe classical Carnot heat engine Branches Classical Statistical Chemical Quantum thermodynamics Equilibrium / Non-equilibrium Laws Zeroth First Second Third Systems Closed system Open system Isolated system State Equation of state Ideal gas Real gas State of matter Phase (matter) Equilibrium Control volume Instruments Processes Isobaric Isochoric Isothermal Adiabatic Isentropic Isenthalpic Quasistatic Polytropic Free expansion Reversibility Irreversibility Endoreversibility Cycles Heat engines Heat pumps Thermal efficiency System propertiesNote: Conjugate variables in italics Property diagrams Intensive and extensive properties Process functions Work Heat Functions of state Temperature / Entropy (introduction) Pressure / Volume Chemical potential / Particle number Vapor quality Reduced properties Material properties Property databases Specific heat capacity c = {\displaystyle c=} T {\displaystyle T} ∂ S {\displaystyle \partial S} N {\displaystyle N} ∂ T {\displaystyle \partial T} Compressibility β = − {\displaystyle \beta =-} 1 {\displaystyle 1} ∂ V {\displaystyle \partial V} V {\displaystyle V} ∂ p {\displaystyle \partial p} Thermal expansion α = {\displaystyle \alpha =} 1 {\displaystyle 1} ∂ V {\displaystyle \partial V} V {\displaystyle V} ∂ T {\displaystyle \partial T} Equations Carnot's theorem Clausius theorem Fundamental relation Ideal gas law Maxwell relations Onsager reciprocal relations Bridgman's equations Table of thermodynamic equations Potentials Free energy Free entropy Internal energy U ( S , V ) {\displaystyle U(S,V)} Enthalpy H ( S , p ) = U + p V {\displaystyle H(S,p)=U+pV} Helmholtz free energy A ( T , V ) = U − T S {\displaystyle A(T,V)=U-TS} Gibbs free energy G ( T , p ) = H − T S {\displaystyle G(T,p)=H-TS} HistoryCulture History General Entropy Gas laws "Perpetual motion" machines Philosophy Entropy and time Entropy and life Brownian ratchet Maxwell's demon Heat death paradox Loschmidt's paradox Synergetics Theories Caloric theory Vis viva ("living force") Mechanical equivalent of heat Motive power Key publications An Inquiry Concerning theSource ...
Ideal gas lawEquation of the state of a hypothetical ideal gas Isotherms of an ideal gas for different temperatures. The curved lines are rectangular hyperbolae of the form y = a/x. They represent the relationship between pressure (on the vertical axis) and volume (on the horizontal axis) for an ideal gas at different temperatures: lines that are farther away from the origin (that is, lines that are nearer to the top right-hand corner of the diagram) correspond to higher temperatures.
ThermodynamicsPhysics of heat, work, and temperature ThermodynamicsThe classical Carnot heat engine Branches Classical Statistical Chemical Quantum thermodynamics Equilibrium / Non-equilibrium Laws Zeroth First Second Third Systems Closed system Open system Isolated system State Equation of state Ideal gas Real gas State of matter Phase (matter) Equilibrium Control volume Instruments Processes Isobaric Isochoric Isothermal Adiabatic Isentropic Isenthalpic Quasistatic Polytropic Free expansion Reversibility Irreversibility Endoreversibility Cycles Heat engines Heat pumps Thermal efficiency System propertiesNote: Conjugate variables in italics Property diagrams Intensive and extensive properties Process functions Work Heat Functions of state Temperature / Entropy (introduction) Pressure / Volume Chemical potential / Particle number Vapor quality Reduced properties Material properties Property databases Specific heat capacity c = {\displaystyle c=} T {\displaystyle T} ∂ S {\displaystyle \partial S} N {\displaystyle N} ∂ T {\displaystyle \partial T} Compressibility β = − {\displaystyle \beta =-} 1 {\displaystyle 1} ∂ V {\displaystyle \partial V} V {\displaystyle V} ∂ p {\displaystyle \partial p} Thermal expansion α = {\displaystyle \alpha =} 1 {\displaystyle 1} ∂ V {\displaystyle \partial V} V {\displaystyle V} ∂ T {\displaystyle \partial T} Equations Carnot's theorem Clausius theorem Fundamental relation Ideal gas law Maxwell relations Onsager reciprocal relations Bridgman's equations Table of thermodynamic equations Potentials Free energy Free entropy Internal energy U ( S , V ) {\displaystyle U(S,V)} Enthalpy H ( S , p ) = U + p V {\displaystyle H(S,p)=U+pV} Helmholtz free energy A ( T , V ) = U − T S {\displaystyle A(T,V)=U-TS} Gibbs free energy G ( T , p ) = H − T S {\displaystyle G(T,p)=H-TS} HistoryCulture History General Entropy Gas laws "Perpetual motion" machines Philosophy Entropy and time Entropy and life Brownian ratchet Maxwell's demon Heat death paradox Loschmidt's paradox Synergetics Theories Caloric theory Vis viva ("living force") Mechanical equivalent of heat Motive power Key publications An Inquiry Concerning theSource ...
KelvinThe kelvin (symbol: K) is the base unit for temperature in the International System of Units (SI).
Rankine scaleThe Rankine scale ( ) is an absolute scale of thermodynamic temperature named after the University of Glasgowengineer and physicistW. J. M. Rankine, who proposed it in 1859. As on the Kelvin scale, which was first proposed in 1848, zero on the Rankine scale is absolute zero, but a temperature difference of one Rankine degree (°R or °Ra) is defined as equal to one Fahrenheit degree, rather than the Celsius degree used on the Kelvin scale.
Compressibility factorIn thermodynamics, the compressibility factor (Z), also known as the compression factor or the gas deviation factor, describes the deviation of a real gas from ideal gas behaviour. It is simply defined as the ratio of the molar volume of a gas to the molar volume of an ideal gas at the same temperature and pressure. It is a useful thermodynamic property for modifying the ideal gas law to account for the real gas behaviour.
State variableA state variable is one of the set of mathematical variables that are used to describe the "state" of a system, e.g. of a dynamical system or a thermodynamical system.
Critical exponentCritical exponents describe the behavior of physical quantities near continuous phase transitions. It is believed, though not proven, that they are universal, i.e. they do not depend on the details of the physical system, but only on some of its general features.Cubic equations of stateCubic equations of state are a specific class of thermodynamic models for modeling the pressure of a gas as a function of temperature and density and which can be rewritten as a cubic function of the molar volume. Equations of state are generally applied in the fields of physical chemistry and chemical engineering, particularly in the modeling of vapor–liquid equilibrium and chemical engineering process design.*As an Amazon Associate I earn from qualifying purchases.