A "salted" nuclear weapon is reminiscent of
fission-fusion-fission weapons, but instead of a fissionable jacket around
the secondary stage fusion fuel, a non-fissionable blanket of a specially
chosen salting isotope is used (cobalt-59 in the case of the cobalt bomb).
This blanket captures the escaping fusion neutrons to breed a radioactive
isotope that maximizes the fallout hazard from the weapon rather than
generating additional explosive force (and dangerous fission fallout) from
fast fission of U-238.
Variable fallout effects can be obtained by
using different salting isotopes. Gold has been proposed for short-term
fallout (days), tantalum and zinc for fallout of intermediate duration
(months), and cobalt for long term contamination (years). To be useful for
salting, the parent isotopes must be abundant in the natural element, and
the neutron-bred radioactive product must be a strong emitter of
penetrating gamma rays.
Table 1.6-1 Candidate Salting Agents
Parent Natural Radioactive Half-Life
Isotope Abundance Product
Cobalt-59 100% Co-60 5.26 years
Gold-197 100% Au-198 2.697 days
Tantalum-181 99.99% Ta-182 115 days
Zinc-64 48.89% Zn-65 244 days
The idea of the cobalt bomb originated with
Leo Szilard who publicized it in Feb. 1950, not as a serious proposal for
weapon, but to point out that it would soon be possible in principle to
build a weapon that could kill everybody on earth (see Doomsday Device in
Questions and Answers). To design such a theoretical weapon a radioactive
isotope is needed that can be dispersed world wide before it decays. Such
dispersal takes many months to a few years so the half-life of Co-60 is
ideal.
The Co-60 fallout hazard is greater than
the fission products from a U-238 blanket because
- many fission-produced isotopes have
half-lives that are very short, and thus decay before the fallout
settles or can be protected against by short-term sheltering;
- many fission-produced isotopes have very
long half-lives and thus do not produce very intense radiation;
- the fission products are not radioactive
at all.
The half-life of Co-60 on the other hand
is long enough to settle out before significant decay has occurred,
and to make it impractical to wait out in shelters, yet is short
enough that intense radiation is produced.
Initially gamma radiation fission
products from an equivalent size fission-fusion-fission bomb are much
more intense than Co-60: 15,000 times more intense at 1 hour; 35 times
more intense at 1 week; 5 times more intense at 1 month; and about
equal at 6 months. Thereafter fission drops off rapidly so that Co-60
fallout is 8 times more intense than fission at 1 year and 150 times
more intense at 5 years. The very long lived isotopes produced by
fission would overtake the again Co-60 after about 75 years.
Zinc has been proposed as an alternate
candidate for the "doomsday role". The advantage of Zn-64 is
that its faster decay leads to greater initial intensity.
Disadvantages are that since it makes up only half of natural zinc, it
must either be isotopically enriched or the yield will be cut in half;
that it is a weaker gamma emitter than Co-60, putting out only
one-fourth as many gammas for the same molar quantity; and that
substantially amounts will decay during the world-wide dispersal
process. Assuming pure Zn-64 is used, the radiation intensity of Zn-65
would initially be twice as much as Co-60. This would decline to being
equal in 8 months, in 5 years Co-60 would be 110 times as intense.
Militarily useful radiological weapons
would use local (as opposed to world-wide) contamination, and high
initial intensities for rapid effects. Prolonged contamination is also
undesirable. In this light Zn-64 is possibly better suited to military
applications than cobalt, but probably inferior to tantalum or gold.
As noted above ordinary "dirty" fusion-fission bombs have
very high initial radiation intensities and must also be considered
radiological weapons.
No cobalt or other salted bomb has ever
been atmospherically tested, and as far as is publicly known none have
ever been built. In light of the ready availability of
fission-fusion-fission bombs, it is unlikely any special-purpose
fallout contamination weapon will ever be developed.
The British did test a bomb that
incorporated cobalt as an experimental radiochemical tracer
(Antler/Round 1, 14 September 1957). This 1 kt device was exploded at
the Tadje site, Maralinga range, Australia. The experiment was
regarded as a failure and not repeated.
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