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The '''second law of thermodynamics''', as formulated in the middle of the 19th century by [[William Thomson]] (Lord Kelvin) and [[Rudolf Clausius]], states that it is impossible to gain mechanical energy by letting heat flow from a ''cold'' to a ''warm'' object.  The law states, on the contrary, that  mechanical energy (work) is needed to transport heat from a low- to a high-temperature heat bath.  
{{Image|Complex number.png|right|350px| Complex number ''z'' &equiv; ''r'' exp(''i''&theta;) multiplied by ''i'' gives <i>z'</i> <nowiki>=</nowiki> <i>z</i>&times;''i''
<nowiki>=</nowiki> ''z'' exp(''i''&thinsp;&pi;/2) (counter clockwise rotation over 90°). Division of ''z'' by ''i'' gives ''z''". Division by ''i'' is multiplication by &minus;''i'' <nowiki> = </nowiki> exp(&minus;''i''&thinsp; &pi;/2) (clockwise rotation over 90°).}}


If the second law would be invalid, there would be no energy crisis. For example, it would be possible—as already pointed out by Lord Kelvin—to fuel ships by energy extracted from sea water. After all, the oceans contain immense amounts of [[internal energy]].  If it would be possible to extract a small portion of this energy—whereby a slight cooling of the sea water would occur—and  to  use this energy to move the ship (a form of work), then the seas could be sailed without any net consumption of energy.  It would ''not'' violate the [[first law of thermodynamics]], because the  the ship's rotating propellers do heat the water and in total the energy of the supersystem "ship-plus-ocean" would be conserved, in agreement with the first law.  Unfortunately, it is not possible, because a ship is warmer than the sea water that it moves in (or at least the ship is not colder) and hence no work can be extracted from the water by the ship.  
==Complex numbers in physics==
===Classical physics===
Classical physics consists of [[classical mechanics]], [[Maxwell's equations|electromagnetic theory]], and phenomenological [[thermodynamics]]. One can add Einstein's special and general theory of [[relativity]] to this list, although this theory, being formulated in the 20th century, is usually not referred to as "classical". In these four branches of physics the basic quantities and equations governing the behavior of the quantities are real.


==Entropy==
Classical mechanics has three different, but equivalent, formulations. The oldest, due to [[Isaac Newton|Newton]], deals with masses and  position vectors of particles, which are real, as is time ''t''. The first and second time derivatives of the position vectors enter Newton's equations and these are obviously real, too. The same is true for [[Lagrange formalism|Lagrange's formulation]] of classical mechanics in terms of position vectors and velocities of particles and for [[Hamilton formalism|Hamilton's formulation]] in terms of [[momentum|momenta]] and positions.
Clausius was able to give a mathematical expression of the second law. In order to be able do that, he needed the concept of [[entropy]]. Following his footsteps entropy will be introduced in this subsection.  


The state of a thermodynamical system is characterized by a number of (dependent) variables, such as [[pressure]] ''p'', [[temperature]] ''T'', amount of substance, volume ''V'', etc. In general a system has a number of energy contacts with its surroundings. For instance, the prototype thermodynamical system, a gas-filled cylinder with piston, can perform work ''DW'' = ''pdV''   on its surroundings, where ''dV'' stands for a small increment of the volume ''V'' of the cylinder, ''p'' is the pressure inside the cylinder and ''DW'' stands for a small amount of work. This small amount is indicated by ''D'', and not by ''d'', because ''DW'' is not necessarily a differential of a function.  However, when we divide by ''p'' the quantity ''DW''/''p'' becomes equal to the differential of the state function ''V''. State functions are local, they dependent on the actual values of the parameters, and not on the path along which the state was reached. Mathematically this means that integration from point 1 to point 2 along path I is equal to integration along another path II
Maxwell equations, that constitute the basis of electromagnetic theory, are in terms of real vector operators ([[gradient]], [[divergence]], and [[curl]]) acting on real [[electric field|electric]] and [[magnetic field|magnetic]] fields.
 
Thermodynamics is concerned with concepts as [[internal energy]], [[entropy]], and [[work]]. Again, these properties are real.  
 
The special theory of relativity is formulated in [[Minkowski space]]. Although this space is sometimes described as a 3-dimensional [[Euclidean space]] to which the axis ''ict'' (''i'' is the imaginary unit, ''c'' is speed of light, ''t'' is time) is added as a fourth dimension, the role of ''i'' is non-essential. The imaginary unit is introduced as a pedestrian way to the computation of the indefinite, real, inner product that in Lorentz coordinates has the metric
:<math>
:<math>
V_2 =  V_1 + {\int\limits_1\limits^2}_{{\!\!}^{(I)}} dV
\begin{pmatrix}
= V_1 + {\int\limits_1\limits^2}_{{\!\!}^{(II)}} dV
-1 & 0 & 0 & 0 \\
\;\Longrightarrow\; {\int\limits_1\limits^2}_{{\!\!}^{(I)}} \frac{DW}{p} =
0 & 1 & 0 & 0 \\
{\int\limits_1\limits^2}_{{\!\!}^{(II)}} \frac{DW}{p}  
0  & 0 & 1 & 0 \\
0  & 0 & 0 & 1 \\
\end{pmatrix},
</math>
</math>
The amount of work (divided by ''p'') performed along path I is equal to the amount of work (divided by ''p'') along path II, which proves that the fraction ''DW''/''p'' is a state variable.  
which obviously is real. In other words, Minkowski space is a space over the real field ℝ.
The general theory of relativity is formulated over  real [[differentiable manifold]]s that  are locally Lorentzian. Further, the Einstein field equations contain mass distributions that are  real.


Absorption of a small amount of heat ''DQ'' is another energy contact of the system with its surroundings. In a completely analogous manner, the following result can be shown for ''DQ'' (divided by ''T'') absorbed by the system along two different paths:
So, although the classical branches of physics do not need complex numbers, this does not mean that these numbers cannot be useful. A very important mathematical technique, especially for those branches of physics where there is flow (of electricity, heat, or mass) is [[Fourier analysis]]. The Fourier series is most conveniently formulated in complex form. Although it would be possible to formulate it in real terms (expansion in terms of sines and cosines) this would be cumbersome, given the fact that the application of the usual trigonometric formulas for the multiplication of sines and cosines is so much more difficult than the corresponding multiplication of complex numbers. Especially electromagnetic theory makes heavy use of complex numbers, but it must be remembered that the final results, that are to be compared with observable quantities, are real.
===Quantum physics===
In quantum physics complex numbers are essential. In the oldest formulation, due to [[Heisenberg]] the imaginary unit appears in an essential way through the canonical commutation relation
:<math>
[p_i,q_j] \equiv p_i q_j - q_j p_i = -i\hbar \delta_{ij},
</math>  
''p''<sub>''i''</sub> and ''q''<sub>''j''</sub> are linear operators (matrices) representing the ''i''th and ''j''th component of the momentum and position of a particle, respectively,.


<div style="text-align: right;" >
The time-dependent [[Schrödinger equation]] also contains ''i'' in an essential manner. For a free particle of mass ''m'' the equation reads
<div style="float: left;  margin-left: 35px;" >
<math>{\int\limits_1\limits^2}_{{\!\!}^{(I)}}\frac{DQ}{T} = {\int\limits_1\limits^2}_{{\!\!}^{(II)}} \frac{DQ}{T}
</math>
</div>
<span id="(1)" style="margin-right: 200px; vertical-align: -40px; ">(1)</span>
</div>
<br><br>
Hence the quantity ''dS'' defined  by
:<math>
:<math>
dS \;\stackrel{\mathrm{def}}{=}\; \frac{DQ}{T}
\frac{\hbar}{2m} \nabla^2 \Psi(\mathbf{r},t) = -i \frac{\partial}{\partial t} \Psi(\mathbf{r},t) .
</math>
</math>
is the differential of a state variable ''S'', the ''entropy'' of the system. Before proving  equation (1) from the second law, it is emphasized that this definition of entropy  only fixes entropy differences:
This equation may be compared to the [[wave equation]] that appears in several branches of classical physics
:<math>
:<math>
S_2-S_1 \equiv \int_1^2 dS = \int_1^2 \frac{DQ}{T}  
v^2 \nabla^2 \Psi(\mathbf{r},t) = \frac{\partial^2}{\partial t^2} \Psi(\mathbf{r},t),
</math>
</math>
Note further that entropy has the dimension energy per degree temperature (joule per degree kelvin) and recalling the [[first law of thermodynamics]]  (the differential ''dU'' of the [[internal energy]] satisfies ''dU'' = ''DQ'' + ''DW''), it follows that
where ''v'' is the [[phase velocity|velocity]] of the waveIt is clear from this similarity why
:<math>
Schrödinger's equation is sometimes called the wave equation of quantum mechanics. It is also clear that the essential difference between quantum physics and classical physics is the first-order time derivative including the imaginary unit. The classical equation is real and has on the right hand side a second derivative with respect to time.
dU = TdS - pdV.\,
</math>
(For convenience sake only a single work term was considered here, namely ''DW'' = ''pdV'').
The internal energy is an extensive quantity, that is, when the system is halved, ''U'' is halved too. The temperature ''T'' is an intensive property, independent of the size of the system. The entropy ''S'', then, is also extensive. In that sense the entropy resembles the volume of the system. An important difference between ''V'' and ''S'' is that  the former is a state variable with a concrete  meaning, whereas the latter is introduced by analogy and therefore is not  easily visualized.


===Proof that entropy is a state variable===
The more general form of the Schrödinger equation is
After equation [[#(1)|(1)]] has been proven, the entropy ''S''  has been shown to be a state variable. The standard proof, as given now, is physical and by means of the construct of [[Carnot cycle]]s and is derived from the Clausius/Kelvin formulation of the second law given in the introduction.
{{Image|Entropy.png|right|350px|Fig. 1 Carnot engine (E) moves to or from condensor (C) heat  from or to infinite heat reservoir (R).}}
 
In figure 1  a two finite heat baths C ("condensors") of constant volume with variable temperature ''T'' are shown. They are connected to an infinite heat reservoir R through  reversible Carnot engines E. Because R is infinite its temperature ''T''<sub>0</sub> is constant, addition or extraction of heat does not change ''T''<sub>0</sub>.  It is assumed that always ''T'' &ge; ''T''<sub>0</sub>. The Carnot engines cycle and per cycle either generate work ''DW''<sub>out</sub> when heat is transported from high temperature to low temperature (path II), or need work  ''DW''<sub>in</sub> when heat is transported from low to high temperature (path I).
 
The definition of [[thermodynamical temperature]]  is such that for path II,
:<math>
:<math>
\frac{DW_\mathrm{out}}{DQ} = \frac{T-T_0}{T},
H \Psi(t) = i \hbar \frac{\partial}{\partial t} \Psi(t) ,
</math>
</math>
while for path I it holds by definition that
where ''H'' is the operator representing the energy of the quantum system under consideration. If this energy is time-independent (no time-dependent external fields interact with the system), the equation can be separated, and the imaginary unit enters fairly trivially through a so-called phase factor,
:<math>
:<math>
\frac{DW_\mathrm{in}}{DQ_0} = \frac{T-T_0}{T_0}.
\Psi(t) = e^{-iEt/\hbar} \Phi\quad\hbox{with}\quad H\Phi = E\Phi.
</math>
</math>
The first law of thermodynamics states that  both I and II, respectively, it holds that
The second equation has the form of an operator [[eigenvalue equation]]. The eigenvalue ''E'' (one of the possible observable values of the energy) is real, which is a fairly deep consequence of the quantum laws.<ref>If ''E'' were complex, two separate measurements would be necessary to determine it. One for its real and one for its imaginary part. Since quantum physics states that a measurement gives a collapse of the wave function to an undetermined state, the measurements, even if they would be made in quick succession, would interfere with each other and energy would be unobservable.</ref> The time-independent function &Phi; can very often be chosen to be real. The exception being the case that ''H'' is not invariant under [[time-reversal]]. Indeed, since the time-reversal operator &theta; is [[anti-unitary]], it follows that
:<math>
:<math>
DW_\mathrm{in} = DQ- DQ_0\quad\hbox{and}\quad DW_\mathrm{out} = DQ- DQ_0
\theta H \theta^\dagger \bar{\Phi} = E \bar{\Phi}
</math>
</math>
For I,
where the bar indicates [[complex conjugation]]. Now, if ''H'' is invariant,
:<math>
:<math>
\begin{align}
\theta H \theta^\dagger = H \Longrightarrow H\bar{\Phi} = E\bar{\Phi}\quad\hbox{and}\quad
\frac{DW_\mathrm{in}}{DQ_0} &= \frac{DQ- DQ_0}{DQ_0} = \frac{DQ}{DQ_0} -1 \\
H\Phi = E\Phi,
&=\frac{T-T_0}{T_0} =  \frac{T}{T_0} - 1 \\
&\Longrightarrow DQ_0 = T_0 \left(\frac{DQ}{T}\right)
\end{align}
</math>
For II,
:<math>
\begin{align}
\frac{DW_\mathrm{out}}{DQ} &= \frac{DQ- DQ_0}{DQ} = 1- \frac{DQ_0}{DQ} \\
&=\frac{T-T_0}{T} =  1- \frac{T_0}{T} \\
&\Longrightarrow DQ_0 = T_0 \left(\frac{DQ}{T}\right)
\end{align}
</math>
</math>
then also the real linear combination <math>\Phi+\bar{\Phi}</math> is an eigenfunction belonging to ''E'', which means that the wave function may be chosen real. If ''H'' is not invariant, it usually is transformed into minus itself. Then <math>\Phi\;</math> and <math>\bar{\Phi}</math> belong to ''E'' and &minus;''E'', respectively, so that they are essentially different and cannot be combined to real form. Time-reversal symmetry is usually broken by magnetic fields, which give rise to interactions linear in spin or orbital [[angular momentum]].
==Note==
<references />

Latest revision as of 08:21, 15 February 2010

PD Image
Complex number zr exp(iθ) multiplied by i gives z' = z×i = z exp(i π/2) (counter clockwise rotation over 90°). Division of z by i gives z". Division by i is multiplication by −i = exp(−i  π/2) (clockwise rotation over 90°).

Complex numbers in physics

Classical physics

Classical physics consists of classical mechanics, electromagnetic theory, and phenomenological thermodynamics. One can add Einstein's special and general theory of relativity to this list, although this theory, being formulated in the 20th century, is usually not referred to as "classical". In these four branches of physics the basic quantities and equations governing the behavior of the quantities are real.

Classical mechanics has three different, but equivalent, formulations. The oldest, due to Newton, deals with masses and position vectors of particles, which are real, as is time t. The first and second time derivatives of the position vectors enter Newton's equations and these are obviously real, too. The same is true for Lagrange's formulation of classical mechanics in terms of position vectors and velocities of particles and for Hamilton's formulation in terms of momenta and positions.

Maxwell equations, that constitute the basis of electromagnetic theory, are in terms of real vector operators (gradient, divergence, and curl) acting on real electric and magnetic fields.

Thermodynamics is concerned with concepts as internal energy, entropy, and work. Again, these properties are real.

The special theory of relativity is formulated in Minkowski space. Although this space is sometimes described as a 3-dimensional Euclidean space to which the axis ict (i is the imaginary unit, c is speed of light, t is time) is added as a fourth dimension, the role of i is non-essential. The imaginary unit is introduced as a pedestrian way to the computation of the indefinite, real, inner product that in Lorentz coordinates has the metric

which obviously is real. In other words, Minkowski space is a space over the real field ℝ. The general theory of relativity is formulated over real differentiable manifolds that are locally Lorentzian. Further, the Einstein field equations contain mass distributions that are real.

So, although the classical branches of physics do not need complex numbers, this does not mean that these numbers cannot be useful. A very important mathematical technique, especially for those branches of physics where there is flow (of electricity, heat, or mass) is Fourier analysis. The Fourier series is most conveniently formulated in complex form. Although it would be possible to formulate it in real terms (expansion in terms of sines and cosines) this would be cumbersome, given the fact that the application of the usual trigonometric formulas for the multiplication of sines and cosines is so much more difficult than the corresponding multiplication of complex numbers. Especially electromagnetic theory makes heavy use of complex numbers, but it must be remembered that the final results, that are to be compared with observable quantities, are real.

Quantum physics

In quantum physics complex numbers are essential. In the oldest formulation, due to Heisenberg the imaginary unit appears in an essential way through the canonical commutation relation

pi and qj are linear operators (matrices) representing the ith and jth component of the momentum and position of a particle, respectively,.

The time-dependent Schrödinger equation also contains i in an essential manner. For a free particle of mass m the equation reads

This equation may be compared to the wave equation that appears in several branches of classical physics

where v is the velocity of the wave. It is clear from this similarity why Schrödinger's equation is sometimes called the wave equation of quantum mechanics. It is also clear that the essential difference between quantum physics and classical physics is the first-order time derivative including the imaginary unit. The classical equation is real and has on the right hand side a second derivative with respect to time.

The more general form of the Schrödinger equation is

where H is the operator representing the energy of the quantum system under consideration. If this energy is time-independent (no time-dependent external fields interact with the system), the equation can be separated, and the imaginary unit enters fairly trivially through a so-called phase factor,

The second equation has the form of an operator eigenvalue equation. The eigenvalue E (one of the possible observable values of the energy) is real, which is a fairly deep consequence of the quantum laws.[1] The time-independent function Φ can very often be chosen to be real. The exception being the case that H is not invariant under time-reversal. Indeed, since the time-reversal operator θ is anti-unitary, it follows that

where the bar indicates complex conjugation. Now, if H is invariant,

then also the real linear combination is an eigenfunction belonging to E, which means that the wave function may be chosen real. If H is not invariant, it usually is transformed into minus itself. Then and belong to E and −E, respectively, so that they are essentially different and cannot be combined to real form. Time-reversal symmetry is usually broken by magnetic fields, which give rise to interactions linear in spin or orbital angular momentum.

Note

  1. If E were complex, two separate measurements would be necessary to determine it. One for its real and one for its imaginary part. Since quantum physics states that a measurement gives a collapse of the wave function to an undetermined state, the measurements, even if they would be made in quick succession, would interfere with each other and energy would be unobservable.