second law of thermodynamics

second law of thermodynamics, statement describing the amount of useful work that can be done from a process that exchanges or transfers heat.

The second law of thermodynamics can be precisely stated in the following two forms, as originally formulated in the 19th century by the Scottish physicist William Thomson (Lord Kelvin) and the German physicist Rudolf Clausius, respectively:

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thermodynamics: The second law of thermodynamics

A cyclic transformation whose only final result is to transform heat extracted from a source which is at the same temperature throughout into work is impossible.

A cyclic transformation whose only final result is to transfer heat from a body at a given temperature to a body at a higher temperature is impossible.

The two statements are in fact equivalent because, if the first were possible, then the work obtained could be used, for example, to generate electricity that could then be discharged through an electric heater installed in a body at a higher temperature. The net effect would be a flow of heat from a lower temperature to a higher temperature, thereby violating the second (Clausius) form of the second law. Conversely, if the second form were possible, then the heat transferred to the higher temperature could be used to run a heat engine that would convert part of the heat into work. The final result would be a conversion of heat into work at constant temperature—a violation of the first (Kelvin) form of the second law.

The concept of entropy was first introduced in 1850 by Clausius as a precise mathematical way of testing whether the second law of thermodynamics is violated by a particular process. The test begins with the definition that if an amount of heat Q flows into a heat reservoir at constant temperature T, then its entropy S increases by ΔS = Q/T. (This equation in effect provides a thermodynamic definition of temperature that can be shown to be identical to the conventional thermometric one.) Assume now that there are two heat reservoirs R₁ and R₂ at temperatures T₁ and T₂. If an amount of heat Q flows from R₁ to R₂, then the net entropy change for the two reservoirs is ΔS is positive, provided that T₁ > T₂. Thus, the observation that heat never flows spontaneously from a colder region to a hotter region (the Clausius form of the second law of thermodynamics) is equivalent to requiring the net entropy change to be positive for a spontaneous flow of heat. If T₁ = T₂, then the reservoirs are in equilibrium and ΔS = 0.

The condition ΔS ≥ 0 determines the maximum possible efficiency of heat engines. Suppose that some system capable of doing work in a cyclic fashion (a heat engine) absorbs heat Q₁ from R₁ and exhausts heat Q₂ to R₂ for each complete cycle. Because the system returns to its original state at the end of a cycle, its energy does not change. Then, by conservation of energy, the work done per cycle is W = Q₁ − Q₂, and the net entropy change for the two reservoirs is To make W as large as possible, Q₂ should be kept as small as possible relative to Q₁. However, Q₂ cannot be zero, because this would make ΔS negative and so violate the second law of thermodynamics. The smallest possible value of Q₂ corresponds to the condition ΔS = 0, yielding This is the fundamental equation limiting the efficiency of all heat engines whose function is to convert heat into work (such as electric power generators). The actual efficiency is defined to be the fraction of Q₁ that is converted to work (W/Q₁).

The maximum efficiency for a given T₁ and T₂ is thus A process for which ΔS = 0 is said to be reversible because an infinitesimal change would be sufficient to make the heat engine run backward as a refrigerator.

As an example, the properties of materials limit the practical upper temperature for thermal power plants to T₁ ≅ 1,200 K. Taking T₂ to be the temperature of the environment (300 K), the maximum efficiency is 1 − 300/1,200 = 0.75. Thus, at least 25 percent of the heat energy produced must be exhausted into the environment as waste heat to avoid violating the second law of thermodynamics. Because of various imperfections, such as friction and imperfect thermal insulation, the actual efficiency of power plants seldom exceeds about 60 percent. However, because of the second law of thermodynamics, no amount of ingenuity or improvements in design can increase the efficiency beyond about 75 percent.

The example of a heat engine illustrates one of the many ways in which the second law of thermodynamics can be applied. One way to generalize the example is to consider the heat engine and its heat reservoir as parts of an isolated (or closed) system—i.e., one that does not exchange heat or work with its surroundings. For example, the heat engine and reservoir could be encased in a rigid container with insulating walls. In this case the second law of thermodynamics (in the simplified form presented here) says that no matter what process takes place inside the container, its entropy must increase or remain the same in the limit of a reversible process. Similarly, if the universe is an isolated system, then its entropy too must increase with time. Indeed, the implication is that the universe must ultimately suffer a “heat death” as its entropy progressively increases toward a maximum value and all parts come into thermal equilibrium at a uniform temperature. After that point, no further changes involving the conversion of heat into useful work would be possible. In general, the equilibrium state for an isolated system is precisely that state of maximum entropy. (This is equivalent to an alternate definition for the term entropy as a measure of the disorder of a system, such that a completely random dispersion of elements corresponds to maximum entropy, or minimum information. See information theory: Entropy.)

So what exactly is the connection between entropy and the second law? Recall that heat at the molecular level is the random kinetic energy of motion of molecules, and collisions between molecules provide the microscopic mechanism for transporting heat energy from one place to another. Because individual collisions are unchanged by reversing the direction of time, heat can flow just as well in one direction as the other. Thus, from the point of view of fundamental interactions, there is nothing to prevent a chance event in which a number of slow-moving (cold) molecules happen to collect together in one place and form ice, while the surrounding water becomes hotter. Such chance events could be expected to occur from time to time in a vessel containing only a few water molecules. However, the same chance events are never observed in a full glass of water, not because they are impossible but because they are exceedingly improbable. This is because even a small glass of water contains an enormous number of interacting molecules (about 10²⁴), making it highly unlikely that, in the course of their random thermal motion, a significant fraction of cold molecules will collect together in one place. Although such a spontaneous violation of the second law of thermodynamics is not impossible, an extremely patient physicist would have to wait many times the age of the universe to see it happen.

The foregoing demonstrates an important point: the second law of thermodynamics is statistical in nature. It has no meaning at the level of individual molecules, whereas the law becomes essentially exact for the description of large numbers of interacting molecules. In contrast, the first law of thermodynamics, which expresses conservation of energy, remains exactly true even at the molecular level.

The example of ice melting in a glass of hot water also demonstrates the other sense of the term entropy, as an increase in randomness and a parallel loss of information. Initially, the total thermal energy is partitioned in such a way that all of the slow-moving (cold) molecules are located in the ice and all of the fast-moving (hot) molecules are located in the water (or water vapour). After the ice has melted and the system has come to thermal equilibrium, the thermal energy is uniformly distributed throughout the system. The statistical approach provides a great deal of valuable insight into the meaning of the second law of thermodynamics, but, from the point of view of applications, the microscopic structure of matter becomes irrelevant. The great beauty and strength of classical thermodynamics are that its predictions are completely independent of the microscopic structure of matter.