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In thermodynamics, the entropy of mixing is the increase in the total entropy when several initially separate systems of different composition, each in a thermodynamic state of internal equilibrium, are mixed without chemical reaction by the thermodynamic operation of removal of impermeable partition(s) between them, followed by a time for establishment of a new thermodynamic state of internal ...
The entropy of the surrounding room decreases less than the entropy of the ice and water increases: the room temperature of 298 K is larger than 273 K and therefore the ratio, (entropy change), of δQ / 298 K for the surroundings is smaller than the ratio (entropy change), of δQ / 273 K for the ice and water system. This is ...
Unlike temperature, the putative entropy of a living system would drastically change if the organism were thermodynamically isolated. If an organism was in this type of "isolated" situation, its entropy would increase markedly as the once-living components of the organism decayed to an unrecognizable mass. [11]
Since an entropy is a state function, the entropy change of the system for an irreversible path is the same as for a reversible path between the same two states. [23] However, the heat transferred to or from the surroundings is different as well as its entropy change. We can calculate the change of entropy only by integrating the above formula.
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.
This is possible provided the total entropy change of the system plus the surroundings is positive as required by the second law: ΔS tot = ΔS + ΔS R > 0. For the three examples given above: 1) Heat can be transferred from a region of lower temperature to a higher temperature in a refrigerator or in a heat pump. These machines must provide ...
Entropy of activation determines the preexponential factor A of the Arrhenius equation for temperature dependence of reaction rates. The relationship depends on the molecularity of the reaction: for reactions in solution and unimolecular gas reactions A = (ek B T/h) exp(ΔS ‡ /R),
The significance of the Nernst heat theorem is that it was later used by Max Planck to give the third law of thermodynamics, which is that the entropy of all pure, perfectly crystalline homogeneous materials in complete internal equilibrium is 0 at absolute zero.