The Britannica Guide to Heat, Force, and Motion by Erik Gregersen

By Erik Gregersen

Some of the worlds commonest tactics and interactions are ruled by way of the legislation of thermodynamics and mechanics. whereas the move, unencumber, or absorption of warmth frequently accompany chemical reactions or look inherent to mechanical structures, also they are commonplace to an individual who has ever frolicked open air on a hot day or touched a sizzling plate. Likewise, any actual bodylarge or small, good or fluidis topic to a variety of forces that set off movement. This exact compendium explores the principles and legislation of either thermodynamics and mechanics in addition to the lives of these people who helped boost those primary components of physics.

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Extra resources for The Britannica Guide to Heat, Force, and Motion

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The term 35 7 The Britannica Guide to Heat, Force, and Motion 7 represents the additional atmospheric work that the system does as it undergoes thermal expansion at constant pressure, and the second term involving represents the internal work that must be done to pull the system apart against the forces of attraction between the molecules of the substance (internal stickiness). Because there is no internal stickiness for an ideal gas, this term is zero, and, from the ideal gas law, the remaining partial derivative is  (36) With these substitutions the equation for CP becomes simply CP = CV + nR (37) cP = cV + R (38) or for the molar specific heats.

The heat of reaction is easy to measure because it simply represents the amount of heat that is given off if the reactants are mixed together in a beaker and allowed to react freely without doing any useful work. The above definition for enthalpy and its physical significance allow the equation for ΔG to be written in the particularly illuminating and instructive form ΔG = ΔH − TΔS. (20) Both terms on the right-hand side represent heats of reaction but under different sets of circumstances. , the amount of heat absorbed from the surroundings in order to hold the temperature constant) when the reaction does no useful work, and TΔS is the heat of reaction when the reaction does maximum useful work in an electrochemical cell.

109 kilojoules per mole∙K, (21) representing the higher degree of disorder when water evaporates and turns to steam. The Gibbs free energy change is ΔG = ΔH − TΔS. In this case the Gibbs free energy change is zero because the water and steam are in equilibrium, and no useful work can be extracted from the system (other than work done against the atmosphere). In other words, the Gibbs free energy per molecule of water (also called the chemical potential) is the same for both liquid water and steam, and so water molecules can pass freely from one phase to the other with no change in the total free energy of the system.

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