Systems, apparatus and methods for separating actinium, radium, and thorium

Patent metadata

Field	Value
Publication number	US-2023402200-A1
Application number	US-202318239013-A
Country	US
Kind code	A1
Filing date	Aug 28, 2023
Priority date	Mar 26, 2018
Publication date	Dec 14, 2023
Grant date	—

Abstract

A method of separating actinium and/or radium from proton-irradiated thorium metal. The thorium metal is irradiated to produce isotopes including thorium, actinium and/or radium. The resultant product is dissolved in solution and a selective precipitant is used to precipitate a bulk portion of the thorium. The precipitated thorium can be recovered. Chromatography is carried out on the remaining solution to remove residual thorium and to separate the actinium from the radium.

First claim

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4 . A method of producing thorium radioisotopes, the method comprising:
irradiating thorium metal to produce thorium radioisotopes; dissolving the irradiated thorium metal in a weak acid to yield a first solution comprising dissolved thorium; adding a selective precipitant and precipitating a bulk portion of the dissolved thorium under precipitation conditions while leaving a second solution; and filtering to separate the precipitated thorium product from the second solution.

5 . The method as defined in claim 4 , wherein the thorium comprises Th-228, the method further comprising using the Th-228 as a generator for producing one or more of Ra-224, Pb-212 or Bi-212.

6 . The method as defined in claim 4 , comprising, after said irradiating but before said dissolving, waiting for a decay period to allow for decay of isotopes having a shorter half-life than Th-228.

7 . The A method as defined in claim 4 , wherein the selective precipitant comprises hydrogen peroxide, oxalic acid or iodic acid.

8 . The method as defined in claim 4 , wherein the weak acid comprises a mineral acid.

9 . The method as defined in claim 4 , wherein the weak acid comprises nitric acid.

10 . The method as defined in claim 4 , wherein the selective precipitant is added in at least a 1.05-fold to 3.0-fold molar excess relative to an amount of thorium metal present during the irradiating step, or wherein the concentration of the selective precipitant in the precipitation conditions initially comprises between about 0.01 M and about 4.0 M.

11 . The method as defined in claim 4 , wherein the precipitation conditions comprise a concentration of weak acid between about 0.005 M to about 4 M.

12 . The method as defined in claim 4 , wherein the precipitation conditions comprise a concentration of nitric acid between about 0.5 M to about 0.75 M.

13 . The method as defined in claim 4 , wherein the precipitation conditions comprise ambient temperature.

14 . The method as defined in claim 4 , wherein the bulk portion of the dissolved thorium comprises at least 60% of the dissolved thorium in the weak acid solution or in the second solution.

15 . The method as defined in claim 4 , further comprising prior to dissolving the irradiated thorium metal in the weak acid, dissolving the irradiated thorium metal and the actinium and/or radium in a strong mineral acid and drying the resulting solution.

16 . The method as defined in claim 15 , wherein the strong mineral acid comprises nitric acid having a concentration of between 8 M and 12 M.

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39 . The method as defined in claim 4 , wherein the thorium comprises Th-228.

40 . The method as defined in claim 4 , wherein the precipitated thorium product is recovered.

41 . The method as defined in claim 40 , wherein the step of recovering the precipitated thorium product comprises redissolving the precipitated thorium to yield a generator solution containing Th-228 radionuclides.

42 . The method as defined in claim 41 , wherein the step of redissolving the precipitated thorium comprises dissolving the precipitated thorium in a strong acid.

43 . The method as defined in claim 41 , further comprising using the generator solution to generate Ra-224, Pb-212 or Bi-212.

44 . The method as defined in claim 4 , further comprising allowing the irradiated thorium metal to decay to allow decay of shorter-lived isotopes other than Th-228.

45 . The method as defined in claim 42 , further comprising evaporating the redissolved precipitated thorium to dryness to produce thorium salts.

46 . The method as defined in claim 45 , further comprising redissolving the thorium salts in a solvent for fine purification of Th-228.

Assignees

• Triumf Inc
• Univ British Columbia

Inventors

• Robertson Andrew Kyle Henderson
• Yang Hua
• Zeisler Stefan
• Schaffer Paul

Classifications

• G21G1/001 Primary

  Recovery of specific isotopes from irradiated targets · CPC title

• C01F17/13

  by using ion exchange resins, e.g. chelate resins · CPC title

• B01D15/1871

  placed in series · CPC title

• B01D15/362

  Cation-exchange · CPC title

• B01D15/363

  Anion-exchange · CPC title