Fluoride volatility explained

Fluoride volatility is the tendency of highly fluorinated molecules to vaporize at comparatively low temperatures. Heptafluorides, hexafluorides and pentafluorides have much lower boiling points than the lower-valence fluorides. Most difluorides and trifluorides have high boiling points, while most tetrafluorides and monofluorides fall in between. The term "fluoride volatility" is jargon used particularly in the context of separation of radionuclides.

Volatility and valence

Valences for the majority of elements are based on the highest known fluoride.

Roughly, fluoride volatility can be used to remove elements with a valence of 5 or greater: uranium, neptunium, plutonium, metalloids (tellurium, antimony), nonmetals (selenium), halogens (iodine, bromine), and the middle transition metals (niobium, molybdenum, technetium, ruthenium, and possibly rhodium). This fraction includes the actinides most easily reusable as nuclear fuel in a thermal reactor, and the two long-lived fission products best suited to disposal by transmutation, Tc-99 and I-129, as well as Se-79.

Noble gases (xenon, krypton) are volatile even without fluoridation, and will not condense except at much lower temperatures.

Left behind are alkali metals (caesium, rubidium), alkaline earth metals (strontium, barium), lanthanides, the remaining actinides (americium, curium), remaining transition metals (yttrium, zirconium, palladium, silver) and post-transition metals (tin, indium, cadmium). This fraction contains the fission products that are radiation hazards on a scale of decades (Cs-137, Sr-90, Sm-151), the four remaining long-lived fission products Cs-135, Zr-93, Pd-107, Sn-126 of which only the last emits strong radiation, most of the neutron poisons, and the higher actinides (americium, curium, californium) that are radiation hazards on a scale of hundreds or thousands of years and are difficult to work with because of gamma radiation but are fissionable in a fast reactor.

Reprocessing methods

Uranium oxides react with fluorine to form gaseous uranium hexafluoride, most of the plutonium reacts to form gaseous plutonium hexafluoride, a majority of fission products (especially electropositive elements: lanthanides, strontium, barium, yttrium, caesium) form nonvolatile fluorides. Few metals in the fission products (the transition metals niobium, ruthenium, technetium, molybdenum, and the halogen iodine) form volatile (boiling point <200 °C) fluorides that accompany the uranium and plutonium hexafluorides, together with inert gases. Distillation is then used to separate the uranium hexafluoride from the mixture.[1] [2]

The nonvolatile alkaline fission products and minor actinides is most suitable for further processing with 'dry' electrochemical processing (pyrochemical) non-aqueous methods. The lanthanide fluorides are difficult to dissolve in the nitric acid used for aqueous reprocessing methods, such as PUREX, DIAMEX and SANEX, which use solvent extraction. Fluoride volatility is only one of several pyrochemical processes designed to reprocess used nuclear fuel.

The Řež nuclear research institute at Řež in the Czech Republic tested screw dosers that fed ground uranium oxide (simulating used fuel pellets) into a fluorinator where the particles were burned in fluorine gas to form uranium hexafluoride.[3]

Hitachi has developed a technology, called FLUOREX, which combines fluoride volatility, to extract uranium, with more traditional solvent extraction (PUREX), to extract plutonium and other transuranics].[4] The FLUOREX-based fuel cycle is intended for use with the Reduced moderation water reactor.[5]

Table of relevant properties

Fluoride
Z
Boiling
°C
Melting
°C
Key halflife
Yield
34 −46.6 −50.8 79Se:65ky .04%
52 −39 −38 127mTe:109d
53 4.8 (1 atm) 6.5 (tripoint) 129I:15.7my 0.54%
42 34 17.4 99Mo:2.75d
94 62 52 239Pu

24ky

43 55.3 37.4 99Tc

213ky

6.1%
93 55.18 54.4 237Np

2.14my

92 56.5 (subl) 64.8 233U

160ky

44 200 (dec) 54 106Ru:374d
45 70 103Rh:stable
75 73.72 48.3 Not FP
35 40.25 −61.30 81Br:stable
53 97.85 9.43 129I:15.7my 0.54%
54 114.25 (subl) 129.03 (tripoint)
51 141 8.3 125Sb:2.76y
44 184 115 106Ru:374d
44 227 86.5 106Ru:374d
41 234 79 95Nb:35d low
46 107Pd:6.5my
50 750 (subl)705 121m1Sn:44y
126Sn:230ky
0.013%
?
40 905 932 (tripoint) 93Zr:1.5my 6.35%
47 1159 435 109Ag:stable
55 1251 682 137Cs

30.2y
135Cs:2.3my

6.19%
6.54%
4 1327 552
37 1410 795
92 1417 1036 233U

160ky

1430 459 stable
1570 454 stable
3 1676 848 stable
19 1502 858 40K:1.25Gy
11 1704 993 stable
90 1680 1110
48 1748 1110 113mCd:14.1y
39 2230 1150 91Y:58.51d
49 >1200 1170
56 2260 1368 140Ba:12.75d
65 2280 1172
64 1231 159Gd:18.5h
61 1338 147Pm:2.62y
63 2280 1390 155Eu:4.76y
60 2300 1374 147Nd:11d
59 1395 143Pr:13.57d
58 2327 1430 144Ce:285d
62 2427 1306 151Sm

90y

0.419%
?
38 2460 1477 90Sr

29.1y

5.8%
57 1493 140La:1.68d

See also

Notes

External links

Notes and References

  1. Web site: An Experience on Dry Nuclear Fuel Reprocessing in the Czech Republic . Uhlir . Jan . OECD Nuclear Energy Agency . 2008-05-21 .
  2. Web site: R&D of Pyrochemical Partitioning in the Czech Republic . Uhlir . Jan . OECD Nuclear Energy Agency . 2008-05-21 .
  3. Web site: Development of Uranium Oxide Powder Dosing for Fluoride Volatility Separation Process . Markvart . Milos . 2008-05-21 . dead . https://web.archive.org/web/20041117063325/http://www.fjfi.cvut.cz/Stara_verze/k417/web_ads/papers/P-g6.pdf . November 17, 2004 .
  4. Web site: Fuel Cycle:Hitachi-GE Nuclear Energy, Ltd.
  5. Web site: Next-generation Nuclear Reactor Systems for Future Energy : HITACHI REVIEW . www.hitachi.com . 17 January 2022 . https://web.archive.org/web/20130219094654/http://www.hitachi.com/rev/field/powersystems/2011342_43332.html . 19 February 2013 . dead.
  6. http://www.sciencenet.cn/upload/blog/file/2008/12/2008121510347360620.pdf CRC Handbook of Chemistry and Physics, 88th Edition
  7. http://www.freepatentsonline.com/5076839.html Precious metal refining with fluorine gas – Patent 5076839