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The entropy of a system depends on its internal energy and its external parameters, such as its volume. In the thermodynamic limit, this fact leads to an equation relating the change in the internal energy to changes in the entropy and the external parameters.
In thermodynamics, a parameter representing the state of disorder of a system at the atomic, ionic, or molecular level; the greater the disorder the higher the entropy. [6] A measure of disorder in the universe or of the unavailability of the energy in a system to do work. [7] Entropy and disorder also have associations with equilibrium. [8]
The entropy of inhomogeneous systems is the sum of the entropies of the various subsystems. The laws of thermodynamics hold rigorously for inhomogeneous systems even though they may be far from internal equilibrium. The only condition is that the thermodynamic parameters of the composing subsystems are (reasonably) well-defined.
The third law of thermodynamics states: As the temperature of a system approaches absolute zero, all processes cease and the entropy of the system approaches a minimum value. This law of thermodynamics is a statistical law of nature regarding entropy and the impossibility of reaching absolute zero of temperature. This law provides an absolute ...
Given a set of extensive parameters X i (energy, mass, entropy, number of particles and so on) and thermodynamic forces F i (related to their related intrinsic parameters, such as temperature and pressure), the Onsager theorem states that [16]
The first law of thermodynamics is essentially a definition of heat, i.e. heat is the change in the internal energy of a system that is not caused by a change of the external parameters of the system. However, the second law of thermodynamics is not a defining relation for the entropy.
The standard state of a material (pure substance, mixture or solution) is a reference point used to calculate its properties under different conditions.A degree sign (°) or a superscript Plimsoll symbol (⦵) is used to designate a thermodynamic quantity in the standard state, such as change in enthalpy (ΔH°), change in entropy (ΔS°), or change in Gibbs free energy (ΔG°).
In solution chemistry and biochemistry, the Gibbs free energy decrease (∂G/∂ξ, in molar units, denoted cryptically by ΔG) is commonly used as a surrogate for (−T times) the global entropy produced by spontaneous chemical reactions in situations where no work is being done; or at least no "useful" work; i.e., other than perhaps ± P dV.