US2025361582A1PendingUtilityA1
Purification of enriched isotopes using a multi-step elution process
Est. expiryMay 23, 2044(~17.8 yrs left)· nominal 20-yr term from priority
C22B 3/42C22B 59/00C22B 3/06
45
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Claims
Abstract
Provided herein are methods for isolating an isotope using cation exchange and a multi-step elution process.
Claims
exact text as granted — not AI-modified1 . A method of isolating an isotope from a composition comprising the isotope and one or more impurities, the method comprising:
a) loading the composition into a cation exchange resin, wherein the isotope and impurities having a positive oxidation state bind to the cation exchange resin; b) passing a dilute acid through the cation exchange resin, thereby eluting impurities having a +1 oxidation state from the cation exchange resin; and c) eluting the isotope from the cation exchange resin by passing a strong acid through the cation exchange resin, thereby obtaining an isotope solution.
2 . The method of claim 1 , wherein the isotope has an oxidation state of +3 or greater.
3 . The method of claim 1 , wherein the isotope is a ytterbium (Yb) isotope or a gadolinium (Gd) isotope.
4 . The method of claim 3 , wherein the isotope is Yb-176, Gd-152, Gd-155, or Gd-160.
5 . The method of claim 1 , wherein the one or more impurities comprise sodium ions, and wherein the sodium ions are eluted from the cation exchange resin in step b).
6 . The method of claim 1 , wherein the dilute acid has a molarity of less than 2M.
7 . The method of claim 6 , wherein the dilute acid has a molarity of 0.2M to 0.8M.
8 . The method of claim 6 , wherein the dilute acid has a molarity of about 0.4M.
9 . The method of claim 6 , wherein the dilute acid is a mineral acid.
10 . The method of claim 9 , wherein the mineral acid is selected from hydrochloric acid, nitric acid, phosphoric acid, sulfuric acid, boric acid, hydrofluoric acid, hydrobromic acid, perchloric acid, and hydroiodic acid.
11 . The method of claim 1 , wherein the strong acid has a molarity of 4M to 8M.
12 . The method of claim 11 , wherein the strong acid has a molarity of about 6M.
13 . The method of claim 11 , wherein the strong acid is a mineral acid.
14 . The method of claim 13 , wherein the mineral acid is selected from hydrochloric acid, nitric acid, phosphoric acid, sulfuric acid, boric acid, hydrofluoric acid, hydrobromic acid, perchloric acid, and hydroiodic acid.
15 . The method of claim 1 , further comprising precipitating the isotope from the isotope solution or drying and calcinating the isotope solution.
16 . The method of claim 15 , further comprising heating the precipitated or calcinated isotope, thereby obtaining an isotope oxide.
17 . The method of claim 16 , further comprising irradiating the isotope oxide.
18 . The method of claim 1 , wherein prior to performing step a), the isotope is captured on a collection target, and wherein the composition comprising the isotope and the one or more impurities is obtained by dissolving the captured isotope from the collection target using an acid; and/or burning the collection target.
19 . The method of claim 18 , wherein the collection target comprises a carbon fiber lattice.
20 . The method of claim 19 , wherein the isotope is captured on the collection target by accelerating ions towards the collection target, applying a magnetic field to the accelerated ions, thereby mass separating the isotope from other ions, and blocking the other ions using a mass-resolving aperture, thereby capturing the isotope on the collection target.Join the waitlist — get patent alerts
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