Thermodynamics: From Wikipedia, The Free Encyclopedia
Thermodynamics: From Wikipedia, The Free Encyclopedia
Thermodynamics: From Wikipedia, The Free Encyclopedia
Typical thermodynamic system, showing input from a heat source (boiler) on the left and
output to a heat sink (condenser) on the right. Work is extracted, in this case by a series of
pistons.
Contents
[hide]
• 1 Starting point and relevance
• 2 History
• 3 The laws of thermodynamics
• 4 Thermodynamic potentials
• 5 Classical thermodynamics
• 6 Statistical mechanics
• 7 Chemical thermodynamics
• 8 Thermodynamic systems
• 9 Conjugate variables
• 10 Thermodynamic instruments
• 11 Thermodynamic states
• 12 Thermodynamic processes
• 13 See also
○ 13.1 Approaches and applied fields
○ 13.2 Other
○ 13.3 Wikibooks
• 14 References
• 15 Further reading
• 16 External links
Internal energy
Enthalpy
Grand potential
Other thermodynamic potentials can be obtained through Legendre transformation. Potentials are
used to measure energy changes in systems as they evolve from an initial state to a final state.
The potential used depends on the constraints of the system, such as constant temperature or
pressure. Internal energy is the internal energy of the system, enthalpy is the internal energy of
the system plus the energy related to pressure-volume work, and Helmholtz and Gibbs energy
are the energies available in a system to do useful work when the temperature and volume or the
pressure and temperature are fixed, respectively.
[edit] Classical thermodynamics
Main article: Classical thermodynamics
Classical thermodynamics is the original early 1800s variation of thermodynamics concerned
with thermodynamic states, and properties as energy, work, and heat, and with the laws of
thermodynamics, all lacking an atomic interpretation. In precursory form, classical
thermodynamics derives from chemist Robert Boyle’s 1662 postulate that the pressure P of a
given quantity of gas varies inversely as its volume V at constant temperature; i.e. in equation
form: PV = k, a constant. From here, a semblance of a thermo-science began to develop with the
construction of the first successful atmospheric steam engines in England by Thomas Savery in
1697 and Thomas Newcomen in 1712. The first and second laws of thermodynamics emerged
simultaneously in the 1850s, primarily out of the works of William Rankine, Rudolf Clausius,
and William Thomson (Lord Kelvin).
[edit] Statistical mechanics
Main article: Statistical mechanics
With the development of atomic and molecular theories in the late 1800s and early 1900s,
thermodynamics was given a molecular interpretation. This field, called statistical mechanics or
statistical thermodynamics, relates the microscopic properties of individual atoms and
molecules to the macroscopic or bulk properties of materials that can be observed in everyday
life, thereby explaining thermodynamics as a natural result of statistics and mechanics (classical
and quantum) at the microscopic level. The statistical approach is in contrast to classical
thermodynamics, which is a more phenomenological approach that does not include microscopic
details. The foundations of statistical thermodynamics were set out by physicists such as James
Clerk Maxwell, Ludwig Boltzmann, Max Planck, Rudolf Clausius and J. Willard Gibbs.
[edit] Chemical thermodynamics
Main article: Chemical thermodynamics
Chemical thermodynamics is the study of the interrelation of energy with chemical reactions or
with a physical change of state within the confines of the laws of thermodynamics. During the
years 1873-76 the American mathematical physicist Josiah Willard Gibbs published a series of
three papers, the most famous being On the Equilibrium of Heterogeneous Substances, in which
he showed how thermodynamic processes could be graphically analyzed, by studying the energy,
entropy, volume, temperature and pressure of the thermodynamic system, in such a manner to
determine if a process would occur spontaneously.[14] During the early 20th century, chemists
such as Gilbert N. Lewis, Merle Randall, and E. A. Guggenheim began to apply the
mathematical methods of Gibbs to the analysis of chemical processes.[15]
[edit] Thermodynamic systems
Main article: Thermodynamic system
An important concept in thermodynamics is the “system”. Everything in the universe except the
system is known as surroundings. A system is the region of the universe under study. A system is
separated from the remainder of the universe by a boundary which may be imaginary or not, but
which by convention delimits a finite volume. The possible exchanges of work, heat, or matter
between the system and the surroundings take place across this boundary. Boundaries are of four
types: fixed, moveable, real, and imaginary.
Basically, the “boundary” is simply an imaginary dotted line drawn around a volume of
something when there is going to be a change in the internal energy of that something. Anything
that passes across the boundary that effects a change in the internal energy of the something
needs to be accounted for in the energy balance equation. That something can be the volumetric
region surrounding a single atom resonating energy, such as Max Planck defined in 1900; it can
be a body of steam or air in a steam engine, such as Sadi Carnot defined in 1824; it can be the
body of a tropical cyclone, such as Kerry Emanuel theorized in 1986 in the field of atmospheric
thermodynamics; it could also be just one nuclide (i.e. a system of quarks) as some are theorizing
presently in quantum thermodynamics.
For an engine, a fixed boundary means the piston is locked at its position; as such, a constant
volume process occurs. In that same engine, a moveable boundary allows the piston to move in
and out. For closed systems, boundaries are real while for open system boundaries are often
imaginary. There are five dominant classes of systems:
1. Isolated Systems – matter and energy may not cross the boundary
2. Adiabatic Systems – heat must not cross the boundary
3. Diathermic Systems - heat may cross boundary
4. Closed Systems – matter may not cross the boundary
5. Open Systems – heat, work, and matter may cross the boundary (often called a control
volume in this case)
As time passes in an isolated system, internal differences in the system tend to even out and
pressures and temperatures tend to equalize, as do density differences. A system in which all
equalizing processes have gone practically to completion, is considered to be in a state of
thermodynamic equilibrium.
In thermodynamic equilibrium, a system's properties are, by definition, unchanging in time.
Systems in equilibrium are much simpler and easier to understand than systems which are not in
equilibrium. Often, when analysing a thermodynamic process, it can be assumed that each
intermediate state in the process is at equilibrium. This will also considerably simplify the
situation. Thermodynamic processes which develop so slowly as to allow each intermediate step
to be an equilibrium state are said to be reversible processes.
[edit] Conjugate variables
Main article: Conjugate variables (thermodynamics)
The central concept of thermodynamics is that of energy, the ability to do work. By the First
Law, the total energy of a system and its surroundings is conserved. Energy may be transferred
into a system by heating, compression, or addition of matter, and extracted from a system by
cooling, expansion, or extraction of matter. In mechanics, for example, energy transfer equals the
product of the force applied to a body and the resulting displacement.
Conjugate variables are pairs of thermodynamic concepts, with the first being akin to a "force"
applied to some thermodynamic system, the second being akin to the resulting "displacement,"
and the product of the two equalling the amount of energy transferred. The common conjugate
variables are:
• Pressure-volume (the mechanical parameters);
• Temperature-entropy (thermal parameters);
• Chemical potential-particle number (material parameters).
[edit] Thermodynamic instruments
Main article: Thermodynamic instruments
There are two types of thermodynamic instruments, the meter and the reservoir. A
thermodynamic meter is any device which measures any parameter of a thermodynamic system.
In some cases, the thermodynamic parameter is actually defined in terms of an idealized
measuring instrument. For example, the zeroth law states that if two bodies are in thermal
equilibrium with a third body, they are also in thermal equilibrium with each other. This
principle, as noted by James Maxwell in 1872, asserts that it is possible to measure temperature.
An idealized thermometer is a sample of an ideal gas at constant pressure. From the ideal gas law
PV=nRT, the volume of such a sample can be used as an indicator of temperature; in this manner
it defines temperature. Although pressure is defined mechanically, a pressure-measuring device,
called a barometer may also be constructed from a sample of an ideal gas held at a constant
temperature. A calorimeter is a device which is used to measure and define the internal energy of
a system.
A thermodynamic reservoir is a system which is so large that it does not appreciably alter its
state parameters when brought into contact with the test system. It is used to impose a particular
value of a state parameter upon the system. For example, a pressure reservoir is a system at a
particular pressure, which imposes that pressure upon any test system that it is mechanically
connected to. The Earth's atmosphere is often used as a pressure reservoir.
It is important that these two types of instruments are distinct. A meter does not perform its task
accurately if it behaves like a reservoir of the state variable it is trying to measure. If, for
example, a thermometer were to act as a temperature reservoir it would alter the temperature of
the system being measured, and the reading would be incorrect. Ideal meters have no effect on
the state variables of the system they are measuring.
[edit] Thermodynamic states
Main article: Thermodynamic state
When a system is at equilibrium under a given set of conditions, it is said to be in a definite state.
The state of the system can be described by a number of intensive variables and extensive
variables. The properties of the system can be described by an equation of state which specifies
the relationship between these variables. State may be thought of as the instantaneous
quantitative description of a system with a set number of variables held constant.
[edit] Thermodynamic processes
Main article: Thermodynamic processes
A thermodynamic process may be defined as the energetic evolution of a thermodynamic
system proceeding from an initial state to a final state. Typically, each thermodynamic process is
distinguished from other processes, in energetic character, according to what parameters, as
temperature, pressure, or volume, etc., are held fixed. Furthermore, it is useful to group these
processes into pairs, in which each variable held constant is one member of a conjugate pair. The
seven most common thermodynamic processes are shown below:
1. An isobaric process occurs at constant pressure.
2. An isochoric process, or isometric/isovolumetric process, occurs at constant volume.
3. An isothermal process occurs at a constant temperature.
4. An adiabatic process occurs without loss or gain of energy by heat.
5. An isentropic process (reversible adiabatic process) occurs at a constant entropy.
6. An isenthalpic process occurs at a constant enthalpy.
7. A steady state process occurs without a change in the internal energy of a system