ASTR 498N Lecture 14 Nuclear burning II
(online at www.astro.umd.edu/~drabin/)
We do not argue with the critic who urges that stars are not hot enough for this process; we tell him to go and find a hotter place.
A. Eddington
Hydrogen burning and the proton-proton chain
In the last lecture, we saw that the first conundrum
of stellar nuclear fusionthe apparently impossibility of overcoming the
Coulomb barrier at achievable temperatures
is solved by quantum tunneling.
The second conundrum arose from the inconvenient fact that the nuclear force between two protons is not quite strong enough to produce a bound state of 2He, so that the most obvious way to kick off hydrogen burning doesn’t work:
H. Bethe found the way around this in 1939: start with the weak interaction
to create deuterium. The bare reaction is always
endothermic because
, but the binding energy of 2H more than compensates and allows the
p
p reaction to be exothermic.
Nevertheless, it is very slow: a
proton in the center of the Sun has to wait almost 1010 y on average
before fusing with another proton. This
sets the timescale for hydrogen burning.
Q What happens to the positron produced by
the pp reaction?
Once deuterons are formed, much faster reactions lead to the production of 4He through the proton-proton chain, summarized below:


The second reaction in the proton-proton chain occurs 17 orders of magnitude faster than the first! In particular, it takes ~1010 y to produce a deuteron but only ~1 s to destroy it. This leads to a very low equilibrium concentration of deuterium, about 1 deuteron for every 1018 protons. In contrast, the terrestrial abundance of 2H is much higher, about 0.015% of all hydrogen. We conclude that terrestrial deuterium was not produced in stars like the Sun (we think that almost all deuterium was produced in the big bang).
Some of you may find the following representation to be visually memorable (I see a guy waving at me):

The relative importance of the three branches of the proton-proton chain is significantly temperature dependent, as shown below:

Although PPIII produces a tiny fraction of the
helium in the Sun, the reaction
produces the most energetic neutrinos and dominates the neutrino signal
measured by detectors based on the reaction
. We will
return to the solar neutrino problem in another lecture.
The CNO cycle
There is a second, independent set of reactions that can produce 4He from H. The so-called “CNO bi-cycle” is in fact dominated by the simpler carbon-nitrogen cycle, illustrated below:

The carbon-nitrogen cycle is not an important source of energy production in the Sun (the split is about 98% proton-proton, 2% carbon-nitrogen) but becomes increasingly important on the upper main sequence. This is because the carbon-nitrogen cycle involves heavy elements, which have high Coulomb barriers. The difficulty of penetrating such barriers leads to fusion rates that increase rapidly with temperature.
The carbon-nitrogen cycle is also important in
determing the relative abundances of 13C, 14N, and 15N. In chemical equilibrium, the relative
abundances of these three nuclei are inversely proportional to their fusion
rates. Since the reaction is
the slowest, the relative abundance of 14N is the largest. Nitrogen in the solar system was primarily
produced by the operation of the carbon-nitrogen cycle in earlier generations
of nearby stars.
The full CNO cycle includes a branch that only occurs about 0.04% of the time:

The following figure compares the rate of energy generation as a function of temperature for the two types of hydrogen burning, PP and CNO:

Over a limited range of temperature, the energy generation rate for each of the processes can be represented by a power law,
The following table shows the temperature dependence of ε0 and ν as a function of temperature for the PP, CNO, and triple-alpha (helium burning) processes:

The temperature dependence of the CNO cycle and triple-alpha process is usually quite steep. Note the general trend, for all processes, that the temperature dependence flattens with increasing temperature while the efficiency ε0 increases.
Helium burning
Carbon-based, oxygen-breathing life forms owe a considerable debt to helium burning in stars, which produces both elements. As in the case of hydrogen burning, the most obvious reaction,
is unstable, with a lifetime of only
yet another
conundrum. Indeed, there are no stable
nuclei with A = 8 or A = 5, which foiled many attempts to find
chains of light-particle reactions that would build up heavier elements. The solution came in 1952, when E. Salpeter
realized that the brief 8Be lifetime is nevertheless long compared
to the mean collision (scattering) time of alpha particles at T ~ 108
K. Thus, even with only one out of 109 nuclei being 8Be,
there is a non-negligible probability that an alpha particle will collide with
the transient nucleus to produce carbon:
However, there is still a problem: the rate for this reaction appears to be too low to enable helium burning in a red giant with a central temperature not much above 108 K. On that basis, F. Hoyle predicted that the reaction must be enhanced by a resonance between the collision energy and an internal energy level of 8Be. Hoyle was even able to predict the energy of the resonance, and it was found almost exactly where predicted.
The triple-alpha process therefore involves the production of an excited state of carbon (12C*) and the decay of a small fraction of the excited nuclei to the ground state (most of them just decay back to 8Be and 4He):
Once some 12C has built up, oxygen and
neon can be produced during helium burning by alpha capture: and (to a
minor extent)
. Further
alpha capture is inhibited by the ever-growing Coulomb barrier of the heavier nuclei.
Again from the perspective of carbon-based life
forms, we note that relative abundance of carbon, oxygen and neon produced by
helium burning is sensitive to seemingly arbitrary details of nuclear
structure. Were the 12C*
resonance a bit less favorably placed, the triple-alpha process would be slower
and the reaction
would predominate, converting most of the carbon to oxygen. Were an excited state of 20Ne of
the correct nuclear parity, as well as being at a resonant energy (which it
is), the
would be
enhanced and most of the oxygen would be converted to neon. These what-if speculations can fuel
interesting musings on the anthropic principle.
Advanced stages of nuclear burning
Sufficiently massive stars (M 8M
) can evolve beyond helium burning to burn heavier elements.
Carbon burning
Carbon burning begins at and
. Carbon burning produces neon,
sodium, and magnesium through the reactions
Q
= 13.9 MeV
Q
= 2.2 MeV
Q
= 4.6 MeV
Q
= –2.6 MeV
Q
= –0.1 MeV
Oxygen burning
Reactions between 12C and 16O are not
important. At carbon-burning
temperatures, the higher Coulomb barrier between carbon and oxygen (Z1Z2
= 48) relative to carbon–carbon (Z1Z2 = 36)
makes the carbon–oxygen rate much slower.
By the time the temperature increases to the point where the rate is
significant, carbon is almost entirely exhausted. Therefore, the next major stage of nuclear burning, commencing at
T 109 K, is 16O
reacting with itself through the channels
Q
= 16.5 MeV
Q
= 7.7 MeV
Q
= 1.5 MeV
Q
= 9.6 MeV
Q
= –0.4 MeV
In both carbon and oxygen burning, the main
reactions result in protons and alpha particles that will quickly react (low
Coulomb barrier) in a network of secondary reactions. These secondary reactions are important in determining isotopic
abundances (for example, ) and also
significant for the net energy generation rates (both through exothermic
reactions and neutrino losses). Free
neutrons play a key role in the synthesis of heavy elements, as we shall
discuss later.
Photodisintegration and neon burning
At T 109 K, a new
type of nuclear reaction becomes possible:
the disintegration of nuclei by thermal photons. Nuclear photodisintegration is the nuclear
analogue of the photoionization of atoms and has nothing to do with spontaneous
nuclear fission. Since nuclear binding
energies are typically 106 times greater than atomic binding
energies, photodisintegration becomes important at a few times 109 K
instead of a few times 103 K.
The first major disintegration reaction is
which competes with the alpha-capture production of neon:
For , the disintegration reaction progressively depletes
20Ne. Some of the remaining 20Ne
can capture an alpha particle to produce 24Mg:
Silicon burning
We might suppose that, if the temperature is high
enough, two magnesium nuclei could fuse to create chromium, , or similarly
for silicon
and iron. In fact, however, another
process takes place before the extreme temperatures necessary to overcome the
Mg
Mg or Si
Si Coulomb barrier are reached. At
, thermal photons begin to have sufficient energy to
initiate the photodisintegration of silicon,
Q
≤ –10.0 MeV
The 4He nuclei thus released can then fuse with other 28Si nuclei to start a sequence of reactions that build up heavier elements by alpha capture:
…
Many other photodisintegration reactions are possible, including the photoejection of protons, neutron, and alpha particles from nuclei lighter than silicon. All these reactions proceed much faster than the initial photodisintegration of silicon, which therefore sets the timescale for the whole process. The bidirectional arrows indicate that the reactions are nearly in thermodynamic equilibrium. In near-equilibrium, the relative abundances of different nuclei can be estimated by the familiar Saha equation. For example, for 28Si and 32S,
where μ is the reduced mass of the 28Si–4He system (3.5 amu) and Q is the energy needed to release an alpha particle from a 32S nucleus,
The Saha equation shows that the relative abundance of 28Si and 32S is governed by the temperature and the concentration of 4He produced by the silicon burning. Because of the Boltzmann factor, more tightly bound nuclei will always be favored. In fact, silicon burning is often described as a nucelar rearrangement process in which alpha particles are preferentially transferred from less to more tightly bound nuclei. If we remember that the curve of binding energy per nucleon rises monotonically from the light elements to a peak at atomic number 56, it is evident that silicon burning tends toward the production of iron-group nuclei (A = 56), i.e., isotopes of Cr, Mn, Fe, Co, and Ni. Elements heavier than this are not formed during silicon burning. The production of the iron group can be thought of as a small net flow (“leakage”) superposed on the much faster inverse (bidirectional) reactions illustrated above.
Iron photodisintegration
At even higher temperatures, , even the tightly bound 56Fe can be
photodisintegrated, with the net result
thereby undoing almost the entire nucleosynthesis
process and aborbing ~100 MeV per reaction of energy from the radiation
field. As the temperature rises above , helium becomes more abundant than iron, and
eventually even helium is disintegrated into protons and neutrons, again
draining energy (28 MeV per reaction) from the photon bath. This energy (to which must be added neutrino
losses) can only be supplied from gravitational contraction. Numerically, the drain is so fierce that the
stellar core must be essentially in free fall.
We have definitely left the arena of quasistatic nuclear burning and
entered the cataclysmic realm of the supernova.
Pair production
A photon with energy can create an e+e–
pair. Although
occurs at
, photons on the high-energy tail of the Planck function produce a
non-negligible population of positrons at temperatures as low as a few times 109 K. This is analogous to the presence of ionized
hydrogen at temperatures considerably below kT = 13.6 eV (corresponding
to
).
Summary of nuclear burning stages

The table reminds us that sharply higher temperatures are necessary to burn anything beyond hydrogen, and that the liberated energy per nucleon is at least an order of magnitude lower. Another dramatic aspect of nuclear burning is highlighted by the following table:

On paper, the various reaction chains and cycles have a certain generic similarity. But contrast the stately pace of hydrogen burning (some 10 million years even in a massive star) with the unimaginable fury of silicon burning: 1 day! It’s no surprise that such a star may be headed for Big Trouble.
Synthesis of elements beyond iron
The creation of elements heavier than iron is a vast and complex topic, with many unsolved problems. Also, a meaningful comparison of theoretical with observed abundances is tied inextricably to an understanding of mass loss in the late stages of stellar evolution and of supernova events—for only those elements that escape into the interstellar medium can be incorporated in later generations of stars. Here we address only the most basic underlying question: given the peak in binding energy per nucleon at the iron group, how is it possible to form heavier elements at all?
The answer is neutron capture. So far we have considered the interactions of charged nuclei, which must overcome a Coulomb barrier, and photodisintegration, which is effective only at very high temperatures. However, free neutrons produced during carbon, oxygen, and silicon burning can be captured by heavy nuclei at relatively low temperatures because of the absence of a Coulomb barrier. Because we can’t give a simple answer to the key question of how many free neutrons are available, we confine ourselves to exposing the types of interactions that are possible.
The element can capture a neutron to create
a heavier isotope of the same element,
If this isotope is stable, the process can be repeated to form and so on. If instead the neutron-rich nucleus is
unstable to beta decay, a different element can be produced through
The new element may in turn be stable, in which case it can capture one or more neutrons, or unstable, in which case it can undergo one or more successive beta decays.
The processes just described involve two types of reactions—neutron captures and beta decays—and two types of nuclei—stable and unstable. Stable nuclei can undergo neutron capture only. Unstable nuclei are susceptible to both neutron capture and beta decay; the outcome depends on the characteristic timescale for neutron capture relative to the radioactive half-life. The beta-decay half life is a nuclear characteristic, independent of external physical conditions. The probability of neutron capture, on the other hand, does depend on the prevailing temperature and neutron density. Thus, neutron capture may proceed either more slowly or more rapidly than beta-decay, depending on physical conditions. The resulting chains of reactions and nuclear products also differ. In a seminal paper—known universally as B2FH—Burbidge, Burbidge, Fowler and Hoyle (1957, Rev. Mod. Phys. 29, 547) referred to the two regimes of neutron capture as s-process (slow) or r-process (rapid). The figure below illustrates how the competing processes of neutron capture and beta decay define reaction paths in the periodic table and allow a nucleus to be labelled s, r, or (s,r) depending on whether it can be produced through the s-process, the r-process, or both (a few proton-rich nuclei are bypassed by both processes). In this way, nuclei heavier than the iron peak can be produced.
