IP Library Granted Patent US 10,998,107
Granted Patent B1
US 10,998,107 · App. 16/118,308 · Granted May 4, 2021

Extractants and extractant compositions for radioisotope and metal recovery

Inventors: Benjamin W. Stein (Los Alamos, NM); Tara E. Mastren (Salt Lake City, UT); Michael E. Fassbender (Los Alamos, NM); Stosh A. Kozimor (Los Alamos, NM)
Assignee: Triad National Security, LLC
G21F9/12B01D15/203B01D15/363C07C327/42G21F9/007G21G1/001G21G2001/0094
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Quick Facts
Patent No.
US 10,998,107
App. No.
16/118,308
Granted
May 4, 2021
Kind
B1
Abstract

Disclosed herein are embodiments of an extractant that can be used for chromatographic isolation of radioisotopes and/or metal species. The extractant can be combined with a support medium to provide an extractant composition that selectively and efficiently binds particular radioisotopes and/or metal species. Also disclosed herein are embodiments of a method for using the disclosed extractant embodiments, as well as embodiments of a method for making the extractant and extractant composition.

Claims (30)

1. A composition, comprising:

a support material; and

an extractant having a structure satisfying Formula I

wherein each R a independently is hydrogen, aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic; and each R b independently is hydrogen, aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic, provided that at least one R a or one R b is aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic.

2. The composition of claim 1 , wherein each R a independently is aliphatic, heteroaliphatic, aryl, aliphatic-aryl, or heteroaliphatic-aryl.

3. The composition of claim 1 , wherein each R b independently is aliphatic, heteroaliphatic, aryl, aliphatic-aryl, or heteroaliphatic-aryl.

4. The composition of claim 1 , wherein each R a independently is alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, aryl, alkyl-aryl, alkenyl-aryl, alkynyl-aryl, heteroalkyl-aryl, heteroalkenyl-aryl, or heteroalkynyl-aryl.

5. The composition of claim 1 , wherein each R b independently is alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, aryl, alkyl-aryl, alkenyl-aryl, alkynyl-aryl, heteroalkyl-aryl, heteroalkenyl-aryl, or heteroalkynyl-aryl.

6. The composition of claim 1 , wherein each R a independently is decyl, nonyl, octyl, septyl, or hexyl.

7. The composition of claim 1 , wherein each R b independently is decyl, nonyl, octyl, septyl, or hexyl.

8. The composition of claim 1 , wherein each R a and R b independently are octyl, 2-ethylhexyl, cyclohexyl, methyl, ethyl, or isopropyl.

9. The composition of claim 1 , wherein each R a is the same and each R b is the same.

10. The composition of claim 1 , wherein each R a is the same as each R b .

11. The composition of claim 1 , wherein the support material is an organic resin or an inorganic, particle-based medium.

12. The composition of claim 1 , wherein the support material is an organic acrylic-based resin.

13. The composition of claim 1 , wherein the support material is a silica-based support.

14. The composition of claim 13 , wherein the extractant is covalently bound to the silica-based support.

15. The composition of claim 1 , wherein the extractant is

16. A method, comprising:

exposing a liquid sample to an extractant composition comprising a support material and an extractant having a structure satisfying Formula I

wherein each R a independently is hydrogen, aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic; and each R b independently is hydrogen, aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic, provided that at least one R a or one R b is aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic; and wherein the liquid sample is exposed to the composition for a time sufficient to promote formation of a complex between the extractant composition and a radioisotope, a metal, and/or any ion thereof present in the liquid sample;

separating the complex from the liquid sample;

exposing the complex to a solution having a pH sufficient to promote dissociation of the radioisotope, the metal, or any ion thereof from the extractant composition; and

isolating the radioisotope, the metal, or any ion thereof.

17. The method of claim 16 , wherein the radioisotope is protactinium, niobium, a protactinium ion, a niobium ion, or any combination thereof; and wherein the sample comprises thorium, iron, zinc, any ion thereof, or any combination thereof.

18. The method of claim 16 , wherein the metal is gold, platinum, silver, palladium, any ion thereof, or any combination thereof; and wherein the sample comprises thorium, iron, zinc, any ion thereof, or any combination thereof.

19. A compound having a structure satisfying Formula I

wherein each R a independently is hydrogen, aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic; and each R b independently is hydrogen, aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic, provided that at least one R a or one R b is aliphatic, heteroaliphatic, aromatic, aliphatic-aromatic, or heteroaliphatic-aromatic and further provided that the compound is not or is other than

20. The compound of claim 19 , wherein the compound is

21. The composition of claim 1 , wherein the extractant is not or is other than

Assignments (3)
CONFIRMATORY LICENSE Recorded May 18, 2020
From: TRIAD NATIONAL SECURITY, LLC
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 052682/0752 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2018
From: LOS ALAMOS NATIONAL SECURITY, LLC
To: TRIAD NATIONAL SECURITY, LLC
Reel/Frame 048007/0803 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2018
From: STEIN, BENJAMIN W.; MASTREN, TARA E.; FASSBENDER, MICHAEL E.; KOZIMOR, STOSH A.
To: LOS ALAMOS NATIONAL SECURITY, LLC
Reel/Frame 047223/0487 →
Continuity (1)
Provisional Application 62553007 · Aug 31, 2017