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14 декабря, 2021
Any of the above-mentioned isotope effects can be used to separate the isotopes. Distillation, gas diffusion, centrifugation, electromagnetic separation, electrolysis, and chemical isotope exchange are widely used methods for isotope separation. A newer, novel method of doing this is laser isotope separation (LIS).
The LIS technique was originally developed in the 1970s as a cost-effective, environmentally friendly way of supplying enriched uranium. The method is based on the fact that different isotopes of the same element absorb different wavelengths of laser light. Therefore, a laser can be precisely tuned to ionize only atoms of the desired isotope, which are then drawn to electrically charged collector plates.
The isotope separation is characterized by the separation factor. In a two- component system, the separation factor (a) is defined as:
Xf(1 ~ X0) = R, (1 — Xi)Xo Ro
where X0 and X, are the molar fraction of one of the isotopes before and after separation, respectively.
In addition, 1 — a is called the enrichment factor.
Since the degree of the isotope effects is usually small, one separation step is frequently not enough to reach a high enough enrichment. In this case, a multistage process in cascade can be applied. The enrichment factor of a separation cascade (A) is proportional to the number of stages (n):
A = an = —1 (3.42)
R0
By increasing n, the enrichment increases proportionally.
The enriched isotopes are used for the production of fuels and moderators of nuclear reactors and nuclear weapons, for analytical purposes (e. g., NMR, Mossbauer spectroscopy), and for the preparation of targets in the production of radioactive isotopes. In Table 3.5, the most important enriched isotopes are listed. Beside enrichment, the depletion of the isotopes can be important for special applications. Depleted 64Zn is used in nuclear industry. The addition of zinc to the cooling water inhibits the corrosion and the formation of 60Co (discussed in Section 7.3) from the steel of the reactor, decreasing the workers’ radiation exposure. Natural zinc contains 48% 64Zn; however, the gamma emitter 65Zn isotope is produced by (n, y) nuclear reaction of 64Zn (discussed in Section 6.3). To avoid the production of 65Zn, depleted MZn (<1%) is produced by centrifugation and applied in nuclear reactors.
Table 3.5 Most Important Enriched (and Depleted) Isotopes |
||
Isotope |
Separation Method |
Application |
2H |
Electrolysis, fractionation, |
Moderator in heavy water, nuclear |
6Li |
distillation, chemical exchange |
reactors, nuclear weapons, NMR spectroscopy |
Electrolysis of LiOH, transfer of |
Production of tritium for nuclear |
|
lithium ions from an aqueous |
weapons and fusion reactor |
|
10B |
solution to a lithium amalgam |
experiments |
Distillation of BF3, exchange with |
Neutron absorber in nuclear |
|
13C |
distillation |
reactors, neutron detection, boron cancer therapy |
Distillation of CO |
Tracer studies, especially in organic chemistry, NMR spectroscopy |
|
15n |
Distillation of NO, exchange between NH3(g) and NH4+ |
Tracer studies |
18O |
Exchange between CO2 and H2O |
Tracer studies, production of 18F isotope for positron emission tomography (PET) |
20Ne |
Thermal diffusion |
Tracer studies |
Electromagnetic separation |
Production of PET isotopes: |
|
67Zn, 68Zn |
67Ga |
|
112Cd |
111In |
|
124Xe |
123i Production of isotopes for radiation therapy: |
|
191Ir |
Electromagnetic separation |
192Ir |
124Xe |
125i |
|
186W |
188Re |
|
Depleted 46Ti |
46Sc |
|
74Se |
Electromagnetic separation |
Production of 75Se for gamma cameras |
depleted 64Zn |
Centrifugation |
Corrosion inhibitor in the cooling water of nuclear reactors |
57Fe 119Sn |
Electromagnetic separation |
Mossbauer spectroscopy |
235U |
Gas diffusion of UF6, electromagnetic separation, centrifugation of UF6, LIS |
Nuclear reactors, nuclear weapons |