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US2875041A - Method of making alloys of beryllium with plutonium and the like - Google Patents

Method of making alloys of beryllium with plutonium and the like Download PDF

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Publication number
US2875041A
US2875041A US480591A US48059155A US2875041A US 2875041 A US2875041 A US 2875041A US 480591 A US480591 A US 480591A US 48059155 A US48059155 A US 48059155A US 2875041 A US2875041 A US 2875041A
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beryllium
plutonium
fluoride
alloy
halide
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US480591A
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Oliver J C Runnalls
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C43/00Alloys containing radioactive materials

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  • This invention relates to the production of alloys of beryllium with one or more of the metals uranium, plutonium, actinium, americium, curium, thorium and cerium. r
  • a halide salt of the metal to be alloyed with the beryllium is heated in the presence of berryllium, to reduce the halide to metal and cause the latter to alloy directly with the beryllium.
  • the heavy metal halides are more stable, thermodynamically, than the beryllium halides, the reducing reaction proceeds to completion it the berryllium halide product is continuously removed by vacuum distillation.
  • the resulting alloy is, therefore, free of fluoride
  • the pressure during the reaction ispreferably maintained at about 10 5 mm. Hg, although other vacuum conditions may be employed.
  • the mass is heated to a temperature of 1000 C. to 1350" C. to insure reduction of the halide of the alloying metal. In each case suflicient beryllium is used to complete the'reduction and yet leave the desired amount of beryllium to be'alloyed with the reduced halide metal.
  • plutonium-beryllium alloys 142 mg. of powdered plutonium fluoride PuF was mixed with 64 mg. of beryllium metal powder, and was placed in a berryllium oxide crucible. The-charge was heated in vacuum at 1150 C. for 1 hour to reduce the plutonium fluoride with the beryllium to distill the beryllium fluoride BeF formed, and to alloy the plutonium with the beryllium. ,Since this alloy did not fuse below 1500 C., it was hard sintered by raising the temperature to 1350 C. for fifteen minutes. The resulting alloy was crystalline, weighing 154 mg. and containing 70% plutonium. The plutonium yield in the reduction, therefore, was 94%.
  • uranium-berryllium alloys 56.5 mg. of powdered uranium fluoride UF, was mixed with 24.2 mg. of beryllium metal powder and placed in a beryllium oxide crucible. The charge was heated in vacuum at.l200 C. for minutes to reduce the uranium fluoride with beryllium, to distill the beryllium fluoride BeF formed and to alloy the uranium with the beryllium.
  • the resulting alloy had melted and formed a, small sphere in the bottom of the crucible.
  • the heat treatment about 50% of the Ra distilled from the crucible but returned to the alloy with a half-life of 11.2 days.
  • Alloys thus prepared of beryllium with plutonium, actinium, americium and/ or curium are useful as neutron source materials. As these metals are normally available in small quantities and are relatively ditficult to handle this method is particularly well adapted to providing such alloys.
  • alloying metals may be incorporated in the berryllium to produce, for example, an alloy of beryllium, uranium and thorium.
  • the fluoride of the alloying metal is the preferred halide.
  • a method of producing alloys of beryllium with plutonium which comprises mixing halide of plutonium with beryllium and heating the mass at 1000" C. to 1350 C. in vacuum to reduce the halide and alloy the reduced metal with beryllium.
  • a method of producing a plutonium-beryllium alloy which comprises mixing plutonium fluoride with beryllium metal, heating the mass in vacuum at about 1150 C. to reduce the fluoride and alloythe metals and removing the volatile beryllium fluoride formed.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Description

slag.
United States Patent lVIETHOD OF MAKING ALLOYS 0F BERYLLIUM WITH PLUTONIUM AND THE LIKE Oliver J. 'C. Runnalls, Deep River, Ontario, Canada, as-
signor, by mesne assignments, to the United States of America as represented by the United States Atomic Energy Commission No Drawing. Application January 7, 1955 7 Serial No. 480,591
4 Claims. (Cl. 75-1223) This invention relates to the production of alloys of beryllium with one or more of the metals uranium, plutonium, actinium, americium, curium, thorium and cerium. r
In accordance with the method of the invention a halide salt of the metal to be alloyed with the beryllium is heated in the presence of berryllium, to reduce the halide to metal and cause the latter to alloy directly with the beryllium. Although the heavy metal halides are more stable, thermodynamically, than the beryllium halides, the reducing reaction proceeds to completion it the berryllium halide product is continuously removed by vacuum distillation. The resulting alloy is, therefore, free of fluoride The pressure during the reaction ispreferably maintained at about 10 5 mm. Hg, although other vacuum conditions may be employed. The mass is heated to a temperature of 1000 C. to 1350" C. to insure reduction of the halide of the alloying metal. In each case suflicient beryllium is used to complete the'reduction and yet leave the desired amount of beryllium to be'alloyed with the reduced halide metal.
The following examples are illustrative of the operation:
1. Preparation of plutonium-beryllium alloys 142 mg. of powdered plutonium fluoride PuF was mixed with 64 mg. of beryllium metal powder, and was placed in a berryllium oxide crucible. The-charge was heated in vacuum at 1150 C. for 1 hour to reduce the plutonium fluoride with the beryllium to distill the beryllium fluoride BeF formed, and to alloy the plutonium with the beryllium. ,Since this alloy did not fuse below 1500 C., it was hard sintered by raising the temperature to 1350 C. for fifteen minutes. The resulting alloy was crystalline, weighing 154 mg. and containing 70% plutonium. The plutonium yield in the reduction, therefore, was 94%.
2. Preparation of uranium-berryllium alloys 56.5 mg. of powdered uranium fluoride UF, was mixed with 24.2 mg. of beryllium metal powder and placed in a beryllium oxide crucible. The charge was heated in vacuum at.l200 C. for minutes to reduce the uranium fluoride with beryllium, to distill the beryllium fluoride BeF formed and to alloy the uranium with the beryllium.
ice
2 The resulting alloy was crystalline, weighing 59.7 mg.
' and containing 69% uranium. The uranium yield in the reduction, therefore was 96%.
3. Preparation of actinium-beryllium alloys 15 me. (200 ,ug.) of Ac as AcCl was evaporated to dryness on oxalic acid along with 50 mg. of uranium as a carrier. The actinium-uranium mixture was calcined to oxide at 600 .C. and fluorinated for 2 hours at 600 C. with a mixture of anhydrous hydrogen fluoride and hydrogen. The resulting fluoride was mixed with beryllium powder to produce a Be to Ac-l-U ratio of about 200 to 1 in the final alloy. The mixture was heated at 5 10- mm. mercury pressure in a beryllium oxide crucible for 15 minutes at 1350 C. to permit the following reaction to go to completion.
The resulting alloy had melted and formed a, small sphere in the bottom of the crucible. During the heat treatment about 50% of the Ra distilled from the crucible but returned to the alloy with a half-life of 11.2 days.
Alloys thus prepared of beryllium with plutonium, actinium, americium and/ or curium are useful as neutron source materials. As these metals are normally available in small quantities and are relatively ditficult to handle this method is particularly well adapted to providing such alloys.
It will, be apparent that more than one of the alloying metals may be incorporated in the berryllium to produce, for example, an alloy of beryllium, uranium and thorium.
The fluoride of the alloying metal is the preferred halide.
What is claimed is:
1. A method of producing alloys of beryllium with plutonium which comprises mixing halide of plutonium with beryllium and heating the mass at 1000" C. to 1350 C. in vacuum to reduce the halide and alloy the reduced metal with beryllium.
2. The method defined in claim 1 wherein the beryllium halide formed is volatilized from the reaction zone.
3. The method defined in claim 1 wherein the halide is fluoride.
4. A method of producing a plutonium-beryllium alloy which comprises mixing plutonium fluoride with beryllium metal, heating the mass in vacuum at about 1150 C. to reduce the fluoride and alloythe metals and removing the volatile beryllium fluoride formed.
References Cited in the file of this patent UNITED STATES PATENTS 1,648,954 Marden Nov. 15, 1927 2,574,627 Daane et al. Nov. 13, 1951 2,592,115 Carroll. Apr. 8, 1952 2,678,267 Saunders May 11, 1954 2,692,823 Cieslicki et al Oct. 26, 1954 2,809,887 Runnalls Oct. 15, 1957 2,826,495 Spedding et a1 Mar. 11, 1958

Claims (1)

1. A METHOD OF PRODUCING ALLOYS OF BERYLLIUM WITH PLUTONIUM WHICH COMPRISES MIXING HALIDE OF PLUTONIUM WITH BERYLLIUM AND HEATING THE MASS AT 1000*C. TO 1350* C. IN VACUUM TO REDUCE THE HALIDE AND ALLOY THE REDUCED METAL WITH BERYLIUM.
US480591A 1955-01-07 1955-01-07 Method of making alloys of beryllium with plutonium and the like Expired - Lifetime US2875041A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2987393A (en) * 1958-11-17 1961-06-06 Ca Atomic Energy Ltd Production of thorium-uranium alloys
US3523869A (en) * 1967-10-03 1970-08-11 Byk Gulden Lomberg Chem Fab Booster-source rods in heavy water moderated reactor
US4509978A (en) * 1982-12-07 1985-04-09 The United States Of America As Represented By The United States Department Of Energy Recoverable immobilization of transuranic elements in sulfate ash

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1648954A (en) * 1921-09-29 1927-11-15 Westinghouse Lamp Co Production of rare metals and alloys thereof
US2574627A (en) * 1947-08-26 1951-11-13 Adrian H Daane Uranium-cobalt alloy
US2592115A (en) * 1948-07-03 1952-04-08 United States Radium Corp Neutron source
US2678267A (en) * 1952-02-27 1954-05-11 Dow Chemical Co Method of making an alloy comprising magnesium and thorium
US2692823A (en) * 1947-08-07 1954-10-26 Marion E Cieslicki Uranium-nickel metal alloy
US2809887A (en) * 1954-10-18 1957-10-15 Oliver J C Runnalls Method of alloying reactive metals with aluminum or beryllium
US2826495A (en) * 1946-07-17 1958-03-11 Frank H Spedding Alloy for use in nuclear fission

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1648954A (en) * 1921-09-29 1927-11-15 Westinghouse Lamp Co Production of rare metals and alloys thereof
US2826495A (en) * 1946-07-17 1958-03-11 Frank H Spedding Alloy for use in nuclear fission
US2692823A (en) * 1947-08-07 1954-10-26 Marion E Cieslicki Uranium-nickel metal alloy
US2574627A (en) * 1947-08-26 1951-11-13 Adrian H Daane Uranium-cobalt alloy
US2592115A (en) * 1948-07-03 1952-04-08 United States Radium Corp Neutron source
US2678267A (en) * 1952-02-27 1954-05-11 Dow Chemical Co Method of making an alloy comprising magnesium and thorium
US2809887A (en) * 1954-10-18 1957-10-15 Oliver J C Runnalls Method of alloying reactive metals with aluminum or beryllium

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2987393A (en) * 1958-11-17 1961-06-06 Ca Atomic Energy Ltd Production of thorium-uranium alloys
US3523869A (en) * 1967-10-03 1970-08-11 Byk Gulden Lomberg Chem Fab Booster-source rods in heavy water moderated reactor
US4509978A (en) * 1982-12-07 1985-04-09 The United States Of America As Represented By The United States Department Of Energy Recoverable immobilization of transuranic elements in sulfate ash

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