Pyrophoric potential of plutonium-containing salt residues
Source abstract
Abstract
Abstract Ignition temperatures of plutonium and the pyrophoric potential of plutonium-containing pyrochemical salt residues are determined from differential thermal analysis (DTA) data and by modeling of thermal behavior. Exotherms observed at 90–200°C for about 30% of the residues are attributed to reaction of plutonium with water from decomposition of hydrated salts. Exotherms observed near 300°C are consistent with ignition of metal particles embedded in the salt. Onset of self-sustained reaction at temperatures as low as 90°C is not precluded by these results and heat-balance models are developed and applied in predicting the static ignition point of massive metal and in evaluating salt pyrophoricity. Results show that ambient temperatures in excess of 200°C are required for ignition of salt residues and that the most reactive salts cannot ignite at low temperatures because diffusion of oxidant to embedded metal is limited by low salt porosity.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Radioactive element chemistry and processing · Nuclear Materials and Properties · Radioactive contamination and transfer
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (23)
Show source-provided references
1. Plutonium vulnerability management plan, US Department of Energy Report DOE/EM-0199, 1995
2. Moser · J. Less-Common Met. · 1984 · 100 · 17110.1016/0022-5088(84)90062-6 ↗
3. Plutonium working group report on environmental, safety and health vulnerabilities associated with the Department’s plutonium storage, US Department of Energy Report DOE/EH-0415, 1994
4. Plutonium storage safety at Major Department of Energy Facilities, Defense Nuclear Facilities Safety Board, Technical Report DNFSB/TECH-1, 1994
5. Transfer and Storage of Plutonium for Fire Safety, Rocky Flats Environmental Technology Site Document PRO-W89-HSP-31.11, Revision 2, 1999
6. Haschke · J. Nucl. Mater. · 1999 · 277 · 17510.1016/S0022-3115(99)00208-1 ↗
7. Haschke · J. Alloys Compd. · 1996 · 243 · 2310.1016/S0925-8388(96)02328-6 ↗
8. Haschke · J Alloys Compounds · 1998 · 271–273 · 21110.1016/S0925-8388(98)00056-5 ↗
9. Stakebake · J. Less-Common Met. · 1986 · 123 · 18510.1016/0022-5088(86)90128-1 ↗
10. J.L. Stakebake, Characterization of the plutonium–water reaction: reaction kinetics between 200°C and 350°C, in: L.R. Morss, J. Fuger (Eds.), Transuranium Elements: A Half Century, American Chemical Society, Washington, 1992, p. 251
11. Martz · J. Nucl. Mater. · 1994 · 210 · 13010.1016/0022-3115(94)90231-3 ↗
12. Haschke · J. Alloys Compounds · 1998 · 266 · 8110.1016/S0925-8388(97)00499-4 ↗
13. Haschke · Science · 2000 · 287 · 28510.1126/science.287.5451.285 ↗
14. Schnizlein · J. Electrochem. Soc. · 1968 · 115 · 46210.1149/1.2411272 ↗
15. J.L. Stakebake, Plutonium pyrophoricity, Report RFP-4517, EG&G Rocky Flats, Inc., Golden, CO, June 199210.2172/5156223 ↗
16. Terada · J. Nucl. Mater. · 1969 · 30 · 34010.1016/0022-3115(69)90251-7 ↗
17. Pitts · Nucl. Safety · 1968 · 9 · 112
18. Stakebake · J. Alloys Compd. · 1993 · 202 · 25110.1016/0925-8388(93)90547-Z ↗
19. T.H. Allen, J.M. Haschke, Hydride-catalyzed corrosion of plutonium by air: initiation by plutonium nonoxide monohydride, Los Alamos National Laboratory Report LA-13462-MS, 199810.2172/663363 ↗
20. Trusell · Anal. Chem. · 1963 · 35 · 67410.1021/ac60199a053 ↗
21. Schnizlein · J. Electrochem Soc. · 1967 · 114 · 2310.1149/1.2426500 ↗
22. Jones · 1993
23. El-Rabi · Int. J. Heat Mass Transfer · 1996 · 19 · 139910.1016/0017-9310(76)90069-7 ↗