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When ΔS > 0 and ΔH < 0, the process is always spontaneous as written. When ΔS < 0 and ΔH > 0, the process is never spontaneous, but the reverse process is always spontaneous. When ΔS > 0 and ΔH > 0, the process will be spontaneous at high temperatures and non-spontaneous at low temperatures. When ΔS < 0 and ΔH < 0, the process will be ...
For a process at constant temperature and pressure without non-PV work, this inequality transforms into <. Similarly, for a process at constant temperature and volume, <. Thus, a negative value of the change in free energy is a necessary condition for a process to be spontaneous; this is the most useful form of the second law of thermodynamics ...
or dG < 0. For a similar process at constant temperature and volume, the change in Helmholtz free energy must be negative, <. Thus, a negative value of the change in free energy (G or A) is a necessary condition for a process to be spontaneous. This is the most useful form of the second law of thermodynamics in chemistry, where free-energy ...
and thus for a system kept at constant temperature and volume and not capable of performing electrical or other non-PV work, the total free energy during a spontaneous change can only decrease. This result seems to contradict the equation dF = −S dT − P dV, as keeping T and V constant seems to imply dF = 0, and hence F = constant.
Spontaneous symmetry breaking is a spontaneous process of symmetry breaking, by which a physical system in a symmetric state spontaneously ends up in an asymmetric state. [ 1 ] [ 2 ] [ 3 ] In particular, it can describe systems where the equations of motion or the Lagrangian obey symmetries, but the lowest-energy vacuum solutions do not exhibit ...
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. When the system is in local equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and ...
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Stimulated Raman spectroscopy, also referred to as stimulated Raman scattering (SRS), is a form of spectroscopy employed in physics, chemistry, biology, and other fields. . The basic mechanism resembles that of spontaneous Raman spectroscopy: a pump photon, of the angular frequency , which is scattered by a molecule has some small probability of inducing some vibrational (or rotational ...