IP Library Granted Patent US 12,398,444
Granted Patent B2
US 12,398,444 · App. 17/366,172 · Granted Aug 26, 2025

Diglycolamide derivatives for separation and recovery of rare earth elements from aqueous solutions

Inventors: Santa Jansone-Popova (Knoxville, TN); Ilja Popovs (Knoxville, TN); Bruce A. Moyer (Oak Ridge, TN)
Assignee: UT-BATTELLE, LLC
C22B59/00B01D11/0492C01F17/17C07C235/06C07D207/08C07D207/12C07D211/42C22B3/282C22B7/007
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,398,444
App. No.
17/366,172
Granted
Aug 26, 2025
Kind
B2
Abstract

Rare earth extractant compounds having the following structure: wherein R 1 , R 2 , R 3 , and R 4 are independently selected from alkyl groups containing 1-30 carbon atoms and optionally containing an ether or thioether linkage connecting between carbon atoms, provided that the total carbon atoms in R 1 , R 2 , R 3 , and R 4 is at least 12; R 5 and R 6 are independently selected from hydrogen atom and alkyl groups containing 1-3 carbon atoms; and provided that at least one of the conditions (i)-(iv) apply as follows: presence of a distal branched group in at least one of R 1 -R 4 (condition i), asymmetry in R 1 -R 4 (condition ii), presence of amine-containing ring (condition iii), or presence of lactam ring (condition iv). Also described are hydrophobic water-insoluble solutions containing at least one extractant compound of Formula (1), as well as method for extracting rare earth elements from aqueous solution by contacting the aqueous solution with the water-insoluble solution.

Claims (19)

1. A rare earth extractant compound having the following structure:

wherein:

R 1 , R 2 , R 3 , and R 4 are independently selected from alkyl groups containing 1-30 carbon atoms and optionally containing an ether or thioether linkage connecting between carbon atoms, provided that the total carbon atoms in R 1 , R 2 , R 3 , and R 4 is at least 12; and R 5 and R 6 are independently selected from hydrogen atom and alkyl groups containing 1-3 carbon atoms; and provided that the following condition applies:

at least one of R 1 , R 2 , R 3 , and R 4 is a distal branched alkyl group constructed of a linear alkyl backbone having at least four carbon atoms with an alpha carbon atom of the linear alkyl backbone attached to a nitrogen atom shown in Formula (1), and the linear alkyl backbone contains a substituting hydrocarbon group at a gamma carbon or higher positioned carbon on the linear alkyl backbone, wherein the substituting hydrocarbon group contains at least two carbon atoms, provided that the distal branched alkyl group contains a total of up to 30 carbon atoms.

2. The compound of claim 1 , wherein the distal branched alkyl group contains at least one substituting hydrocarbon group located at a gamma carbon of the linear alkyl backbone.

3. The compound of claim 1 , wherein the distal branched alkyl group contains at least one substituting hydrocarbon group located at a delta carbon of the linear alkyl backbone.

4. The compound of claim 1 , wherein the distal branched alkyl group contains at least one substituting hydrocarbon group located at an epsilon carbon of the linear alkyl backbone.

5. The compound of claim 1 , wherein the distal branched alkyl group contains at least two substituting hydrocarbon groups located at gamma or higher carbon positions of the linear alkyl backbone.

6. A liquid solution useful for extracting rare earth elements from aqueous solutions, the solution comprising a rare earth extractant compound dissolved in an aqueous-insoluble hydrophobic solvent, wherein the rare earth extractant compound has the following structure:

wherein:

R 1 , R 2 , R 3 , and R 4 are independently selected from alkyl groups containing 1-30 carbon atoms and optionally containing an ether or thioether linkage connecting between carbon atoms, provided that the total carbon atoms in R 1 , R 2 , R 3 , and R 4 is at least 12; and R 5 and R 6 are independently selected from hydrogen atom and alkyl groups containing 1-3 carbon atoms; and provided that of the following condition applies:

at least one of R 1 , R 2 , R 3 , and R 4 is a distal branched alkyl group constructed of a linear alkyl backbone having at least four carbon atoms with an alpha carbon atom of the linear alkyl backbone attached to a nitrogen atom shown in Formula (1), and the linear alkyl backbone contains a substituting hydrocarbon group at a gamma carbon or higher positioned carbon on the linear alkyl backbone, wherein the substituting hydrocarbon group contains at least two carbon atoms, provided that the distal branched alkyl group contains a total of up to 30 carbon atoms.

7. The liquid solution of claim 6 , wherein the aqueous-insoluble hydrophobic solvent is a hydrocarbon solvent.

8. The liquid solution of claim 6 , wherein the liquid solution further comprises an organoamine soluble in the aqueous-insoluble hydrophobic solvent.

9. The liquid solution of claim 8 , wherein the organoamine contains at least one hydrocarbon group containing at least four carbon atoms.

10. The liquid solution of claim 6 , wherein the liquid solution further comprises an alcohol soluble in the aqueous-insoluble hydrophobic solvent, and wherein the alcohol contains at least six carbon atoms.

11. The compound of claim 1 , wherein the substituting hydrocarbon group contains at least three carbon atoms, provided that the distal branched alkyl group contains a total of up to 30 carbon atoms.

12. The compound of claim 1 , wherein the substituting hydrocarbon group contains at least four carbon atoms, provided that the distal branched alkyl group contains a total of up to 30 carbon atoms.

13. The compound of claim 1 , wherein the rare earth extractant compound has the following structure:

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2022
From: JANSONE-POPOVA, SANTA; POPOVS, ILJA; MOYER, BRUCE A.
To: UT-BATTELLE, LLC
Reel/Frame 059513/0852 →
CONFIRMATORY LICENSE Recorded Dec 17, 2021
From: UT-BATTELLE, LLC
To: U. S. DEPARTMENT OF ENERGY
Reel/Frame 058419/0975 →
Continuity (2)
Provisional Application 63048237 · Jul 6, 2020
Related Publication 20220002229A1 · Jan 6, 2022
References Cited (46)
US 7157022B2 · Horwitz et al. · 2007 [cited by applicant]
US 8354085B1 · Guelis · 2013 [cited by applicant]
US 9968887B2 · Bhave et al. · 2018 [cited by applicant]
US 11040296B2 · Brigham · 2021 [cited by examiner]
US 20040062695A1 · Horwitz et al. · 2004 [cited by applicant]
US 20140072485A1 · Luo et al. · 2014 [cited by applicant]
US 20150292061A1 · Fassbender et al. · 2015 [cited by applicant]
US 20190287691A1 · Abergel et al. · 2019 [cited by applicant]
US 20190338394A1 · Brown et al. · 2019 [cited by applicant]
US 20190344198A1 · Brigham et al. · 2019 [cited by applicant]
US 20200122118A1 · Jansone-Popova · 2020 [cited by applicant]
US 20220002840A1 · Jansone-Popova · 2022 [cited by examiner]
US 20220010409A1 · Andreiadis · 2022 [cited by examiner]
AU 2019250770A1 · 2020 [cited by applicant]
CN 101323906A · 2008 [cited by applicant]
CN 106834680A · 2017 [cited by applicant]
CN 106834758A · 2017 [cited by applicant]
CN 106929675A · 2017 [cited by applicant]
FR 2907346A1 · 2008 [cited by applicant]
FR 2948384A1 · 2011 [cited by applicant]
FR 2968014A1 · 2012 [cited by applicant]
IN 106834757A · 2017 [cited by applicant]
JP 2004212076A · 2004 [cited by applicant]
JP 2005201729A · 2005 [cited by applicant]
JP 2006153790A · 2006 [cited by applicant]
JP 2009132953A · 2009 [cited by applicant]
JP 2011169888A · 2011 [cited by applicant]
JP 2014105200A · 2014 [cited by applicant]
JP 2016061580A · 2016 [cited by applicant]
JP 2016065277A · 2016 [cited by applicant]
JP 2018066709A · 2018 [cited by applicant]
RU 2603405C1 · 2016 [cited by applicant]
WO 2011012579A1 · 2011 [cited by applicant]
WO 2012069573A1 · 2012 [cited by applicant]
WO 2015076911A2 · 2015 [cited by applicant]
WO 2016004770A1 · 2016 [cited by applicant]
WO 2016182472A1 · 2016 [cited by applicant]
WO 2018035020A1 · 2018 [cited by applicant]
WO 2019197792A1 · 2019 [cited by applicant]
International Search Report and Written Opinion dated Dec. 23, 2021 issued in PCT/US21/40231, 8 pages. [cited by applicant]
International Search Report and Written Opinion dated Oct. 13, 2021 issued in PCT/US 21/40229, 10 pages. [cited by applicant]
Stamberga, D., et al., “Structure Activity Relationship Approach toward the Improved Separation of Rare-Earth Elements Using Diglycolamides”, Inorg. Chem. 2020, Received Sep. 25, 2020, Published Nov. 13, 2020, pp. 17620… [cited by applicant]
Office Action dated Feb. 27, 2024 received in U.S. Appl. No. 17/366,185, 21 pages. [cited by applicant]
Ravi J. et al., “New Unsymmetrical Digycolamide Ligands for Trivalent Actinide Separation”, Radiochim. Acta 102 (7):609-617 (Mar. 19, 2014). [cited by applicant]
European Supplementary Extended Search Report dated Jun. 5, 2025 received in European Application No. 21 83 7547.5. [cited by applicant]
European Supplementary Extended Search Report dated Jun. 5, 2025 received in European Application No. 21 83 7748.9. [cited by applicant]