Claims
- 1. Method for the manufacture of sintered oxidic nuclear fuel bodies comprising molding nuclear fuel starting powder selected from the group consisting of uranium oxide starting powder, a mixture of uranium oxide and plutonium oxide starting powder, and uranium-plutonium oxide mixed crystal starting powder to form blanks and heat treatment of the blanks with a U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase developed in them to a degree which can be crystallographically detected at a sintering temperature in the range of 1000.degree. to 1400.degree. C. in an oxidizing gas atmosphere and subsequently in a reducing gas atmosphere, in combination with:
- (1) preroasting at least one of (a) blanks formed of nuclear fuel starting powder and (b) the nuclear fuel starting powder at a roasting temperature below the sintering temperature in a roasting gas atmosphere with oxidizing action and with an oxygen potential in which the U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase is developed
- (2) cooling-down the preroasted blanks or the preroasted starting powder to a starting temperature below the roasting temperature in an inert or oxidizing cooling-down gas atmosphere while maintaining the U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase, and subsequent to cooling-down, molding the preroasted starting powder to form blanks, and
- (3) heating the blanks with a U.sub.4 O.sub.9 or (U,PU).sub.4 O.sub.9 crystal phase in them from the starting temperature to the sintering temperature in an inert or oxidizing heating gas atmosphere while maintaining the U.sub.4 O.sub.9 or the (U,Pu).sub.4 O.sub.9 crystal phase.
- 2. Method according to claim 1, wherein the starting powder is preroasted to develop at least 20% by weight U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase.
- 3. Method according to claim 2, wherein the starting powder is preroasted to convert it completely into the U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase.
- 4. Method according to claim 2, wherein the preroasted starting powder after cooling down to the starting temperature is mixed with a quantity of a nuclear fuel powder selected from the group consisting of uranium oxide, plutonium oxide and uranium-plutonium oxide mixed crystal starting powder to form a powder mixture with a content of U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase of at least 20% by weight.
- 5. Method according to claim 1, wherein the blanks are molded of nuclear fuel starting powder and subsequently preroasted to develop at least 20% by weight U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase.
- 6. Method according to claim 5, wherein the blanks are preroasted to convert them completely into the U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase.
- 7. Method according to claim 1, wherein the starting powder or the blanks formed of starting powder are preroasted in the oxidizing roasting gas atmosphere with an oxygen potential at which the U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase is developed and in addition a U.sub.3 O.sub.8 or (U,Pu).sub.3 O.sub.8 crystal phase is formed to a crystallographically detectable extent.
- 8. Method according to claim 1, wherein the roasting gas atmosphere is a mixture of gases selected from the group consisting of carbon dioxide and oxygen, nitrogen with oxygen, and air at atmospheric pressure.
- 9. Method according to claim 1, wherein the starting temperature for heating the blanks with a U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase in them is in the range of 20.degree. C. to 30.degree. C.
- 10. Method according to claim 1, wherein the starting temperature for heating the blanks with a U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase in them is at the ambient temperature.
- 11. Method according claim 2, wherein the roasting temperature is in the range of 70.degree. C. to 400.degree. C. and the preroasting time is in the range of 10 minutes to 6 hours.
- 12. Method according claim 3, wherein the roasting temperature is in the range of 70.degree. C. to 400.degree. C. and the preroasting time is in the range of 10 minutes to 6 hours.
- 13. Method according to claim 11, wherein the roasting temperature is in the range of 70.degree. C. to 200.degree. C. and the preroasting time is in the range of 10 minutes to 2 hours.
- 14. Method according to claim 11, wherein the roasting temperature is in the range of 200.degree. C. to 400.degree. C. and the preroasting time is in the range of 10 minutes to 30 minutes.
- 15. Method according to claim 1, wherein the starting powder is generated as uranium oxide or uranium-plutonium oxide crystal or mixtures thereof with a powder temperature above the roasting temperature, and is first cooled down in an inert gas atmosphere; and wherein the starting powder is then preroasted from an upper temperature limit to a lower temperature limit in the oxidizing roasting gas atmosphere, and is finally cooled-down in the cooling-down gas atmosphere to the starting temperature.
- 16. Method according to claim 15, wherein the upper temperature limit is in the range of 170.degree. C. to 280.degree. C. and the lower temperature in the range of 120.degree. C. to 150.degree. C.
- 17. Method according to claim 16, wherein the upper temperature limit is 250.degree. C. and the lower temperature limit is 130.degree. C.
- 18. Method according to claim 15, wherein the starting powder is cooled-down during the preroasting between the upper and the lower temperature limit with a starting rate in the range of 10.degree. C./minute to 20.degree. C./minute and with a final rate of about 0.1.degree. C./minute.
- 19. Method according to claim 15, wherein the starting powder is stirred during preroasting in a reaction vessel in the roasting gas atmosphere with oxidizing action and with an oxygen potential in which the U.sub.4 O.sub.9 or (U,Pu).sub.4 O.sub.9 crystal phase is developed, and is cooled from the upper to the lower temperature limit by heat transfer to a coolant in a double wall of the reaction vessel.
- 20. Method according to claim 19, wherein the coolant is filled into the double wall of the reaction vessel with a starting temperature in the range of 20.degree. C. to 30.degree. C.
- 21. Method according to claim 1, wherein the cooling gas atmosphere contains a gas selected from the group consisting of air, nitrogen, a rare gas, a mixture of carbon dioxide and oxygen or a mixture of nitrogen and oxygen.
- 22. Method according to claim 1, wherein the heating gas atmosphere has a pressure in the range of 1 to 1.5 bar and contains a gas selected from the group consisting of a rare gas, nitrogen or carbon dioxide.
Priority Claims (1)
Number |
Date |
Country |
Kind |
3519825 |
Jun 1985 |
DEX |
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Parent Case Info
This application is a continuation of application Ser. No. 870,226, filed June 3, 1986, now abandoned.
US Referenced Citations (4)
Number |
Name |
Date |
Kind |
4052330 |
Jensen et al. |
Oct 1977 |
|
4348339 |
Assmann et al. |
Sep 1982 |
|
4438050 |
Dorr et al. |
Mar 1984 |
|
4578229 |
Assmann et al. |
Mar 1986 |
|
Foreign Referenced Citations (1)
Number |
Date |
Country |
0078428 |
May 1983 |
EPX |
Non-Patent Literature Citations (1)
Entry |
Bailor, et al., ed. 1973, Comprehensive Inorganic Chemistry, Pergamon Press, Australia, pp. 225-231. |
Continuations (1)
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Number |
Date |
Country |
Parent |
870226 |
Jun 1986 |
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