Week 1 Flashcards
When a process occurs in a fluid element that is in equilibrium at all times
Write dQ = Tds
It is convenient to define quantities on a per baryon basis as baryon number is a conserved quantity. Then the first law of thermodynamics take on what form?
The general form dQ=d(E/n)+Pd(1/n), where dQ is the heat gained per baryon, P is the pressure, and 1/n is the volume per baryon.
This is addition to the simplifying assumption, dQ=Tds
In general, the energy density of a system containing different species depends on the relative amounts of each species, as well as the volume (1/n) and the adiabat (value of s). Therefore we write the concentration of the ith species of particle by Yi = ni/n, where ni is the number density of particle i. Then what form does the energy take?
E = E(n,s,Yi), where E is the energy per baryon.
Therefore we should write in general d(E/n) = -Pd(1/n)+Tds+Sum(muidYi),
where P = -d(E/n)/d(1/n) = n^2*d(E/n)/dn,
T = d(E/n)/ds,
mui = d(E/n)/dYi = dE/dni.
The quantity mui is called the chemical potential of species i. It has the interpretation of the change in energy density of species i, while the volume, entropy, and all number densities are kept constant. Note that since E is defined to include the rest-mass energy, so is mui!
In equilibrium reactions between the particles produce a state of detailed balance where each reaction is balanced by its inverse and the concentration of each species remains constant. Thus in equilibrium, the concentrations Yi are not independent of the other thermodynamic quantities. We can determine equilibrium relations in what way?
Consider first the special case where the system is infinitesimally close to equilibrium, but the sytem is kept thermally isolated (dQ=0) and at constant volume (dn=0) so that no work is done on the system. In this case, dQ=d(E/n)+Pd(1/n) gives d ( E / n ) = 0; that is, the energy of the system remains constant. Entropy is generated by the reactions, but because entropy is a maximum in equilibrium (from the second law of thermodynamics), ds = 0 to first order. Thus we get that Sum(muidYi)=0
Suppose, for example, one is considering the reaction
e-+p++ n+ve in equilibrium. Then dYe = dYP = - dYn = - dY, and so
mue + mup = mun + munu(e
Then the Sum(mui*Yi)=0 gives the concentrations n as a function s or E. Even wken the initial state is very far from equilibrium, if the system proceeds to equilibrium with dQ = 0 and dn = 0, then its energy still remains constant. Eventually it will be infinitesimally close to equilibrium and the above argument will apply. Thus the composition can again be determined if the chemical potentials are known at the fixed values of n and E.
Now consider the general case where the system is not necessarily thermally isolated, and work may be done on the system. If the system were to achieve equilibrium by quasistatic reactions, then Tds = dQ. In general, however, the second law implies
dQ
d(E/n) + Pd(1/n)
Quantities like energy, volume, entropy, and number of particles are extensive quantities: if one divides a given volume in two by means of a partition, the energy, entropy, and number of particles on each side are half of their values for the whole volume. Quantities like pressure and temperature which remain the same are called intensive quantities. The requirement that all the extensive quantities of the system scale with volume in the same way leads to the relation
g = Sum(mui*Yi), where g is the Gibbs free energy and is written as dg = 1/ndP - sdT+Sum(mui*Yi)
Let us be a little more precise about the number of independent thermody- namic quantities required to specify an equilibrium state. Consider, by way of illustration, an interacting mixture of baryons (including, e.g., neutrons and protons) and leptons (including electrons and muons and their associated neutri- nos). All reactions in a given volume will conserve baryon number density n, electron lepton number den~ity,n,~, muon lepton number density, nLp, and electric charge density nQ. Choose four basic chemical potentials corresponding to these four conserved quantities. For example, choose these to be p p (associated with n), pn(associated with n,,), p,, (associated with nLp),and p, (associated with no). Then in equilibrium all other chemical potentials will be linear combinations of these four. Now in equilibrium all thermodynamic quantities associated with species i are functions only of T and p,. (In the next section, we will see this explicitly for ideal gases.) Thus in general one needs to specify T and four of the p,’s for a complete description of the equilibrium state. Equivalently, one needs to specify any five independent thermodynamic quantities. Usually nQ = 0, so only four quantities are required.
In some situations the concept of a limited equilibrium applies. This means that certain reactions necessary to acheve complete equilibrium are too slow on the timescale of interest. This implies that there will be more than four conserved quantities, and one has to specify more n,’s to describe the system. For example, the dynamical timescale of a star is generally much shorter than the timescale to change its composition by nuclear reactions. To determine the pressure, internal energy, and so on in the star, one has to specify the concentration of H, He, and so on explicitly, and not simply the baryon density n . A similar situation prevails for chemical reactions in a terrestrial laboratory.
In lunetic theory, the number density in phase space for each species of particle, dN/d3x d3p,provides a complete description of the system. Equivalently,one can specify the dimensionless distribution function in phase space, f(x, p, t ) , defined by
dN/d3xd3p = (g/h^3)*f, where h is Plancks constant, g the statistical weight (2S+1), for photons g=2 and for neutrinos g=1. The functionfgives the average occupation number of a cell in phase space. d3xd3p is a Lorentz invariant (i.e., scalar under Lorentz transformations) and hence f is also.
Convenient form of velocity
v = pc2/E
What are two examples of f (the distribution function)
The fermi and bose distributions, f(E) = 1/(exp((E-mu)/kT)+/-1)
For completely degenerate Fermions we use what function?
f(E)=1 if EEFermi
An isolated whte dwarf or neutron star ultimately cools to zero temperature, and it is the pressure associated with matter at T = 0 that supports these stars against gravitational collapse. The simplest cold, degenerate equation of state is that due to a single species of ideal (noninteracting) fermions. For definiteness, let us take the gas to be one of electrons at zero temperature. The gas can be treated as ideal if we ignore all electrostatic interactions. Then how do we define the Fermi Momentum?
EF =(pF2c2+me2c4)1/2
What is the relativity parameter?
x=pF/(me*c)
Even in applications where degenerate electrons contribute most of the pres- sure, the density is usually dominated by
the rest-mass of the ions. This density is Sum(ni*mi)
What is the mean Baryon rest mass
mB=1/n*Sum(nimi) = Sum(nimi)/Sum(niAi). This allows us to define the density of the gas in terms of the abundance of baryons times the mean Baryon rest mass. or also as the abundance of electrons times the mean baryon rest mass divided by the mean number of electrons.