IP Library Granted Patent US 11,858,825
Granted Patent B2
US 11,858,825 · App. 17/088,784 · Granted Jan 2, 2024

Preparation of acid-deficient uranyl nitrate solutions

Inventors: Daniel Brown (Knoxville, TN); Nicholas Linneen (Knoxville, TN)
Assignee: X Energy, LLC
C01F17/276
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Quick Facts
Patent No.
US 11,858,825
App. No.
17/088,784
Granted
Jan 2, 2024
Kind
B2
Abstract

A solution of acid deficient uranyl nitrate has a formula of UO 2 (OH) y (NO 3 ) 2-y , where y ranges from 0.1 to 0.5. The solution is prepared by placing U x O z in aqueous nitric acid to produce a uranium solution, wherein x is 1 to 3 and z is 2 to 8; placing the uranium solution under a pressure greater than atmospheric pressure in a sealed reaction chamber; and heating the uranium solution to a desired temperature of between 150° C. and 250° C. by applying microwave energy to the uranium solution. The uranium solution is maintained at the desired temperature under a pressure of from 5 atmospheres to 40 atmospheres for a hold time of 15 minutes to 6 hours to produce the desired acid deficient uranyl nitrate.

Claims (37)

1. A method of preparing a solution of acid deficient uranyl nitrate having a formula of UO 2 (OH) y (NO 3 ) 2-y , where y ranges from 0.1 to 0.5, the method comprising:

a) dissolving U x O z in aqueous nitric acid to produce a uranium solution, wherein x is 1 to 3 and z is 2 to 8;

b) placing the uranium solution under a pressure greater than atmospheric pressure in a sealed reaction chamber;

c) heating the uranium solution to a desired temperature of between 150° C. and 250° C. by applying microwave energy to the uranium solution;

d) maintaining the uranium solution at the desired temperature under elevated pressure for a desired hold time;

e) partially venting the pressure on the uranium solution without allowing the uranium solution to boil; and

f) reducing the desired temperature to below 100° C. and reducing the pressure on the uranium solution to atmospheric pressure to obtain an acid deficient uranyl nitrate solution.

2. The method of claim 1 , wherein U x O z is dissolved in aqueous nitric acid.

3. The method of claim 1 , wherein U x O z is UO 2 , UO 3 , or U 3 O 8 .

4. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a uranium concentration of from 0.5 M to 3 M and a density of 1.15 g/cm 3 to 1.95 g/cm 3 .

5. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a uranium concentration of from 1 M to 3 M and a density of 1.30 g/cm 3 to 1.95 g/cm 3 .

6. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a uranium concentration of from 2 M to 3 M and a density of 1.55 g/cm 3 to 1.95 g/cm 3 .

7. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a uranium concentration of from 2.5 M to 3 M and a density of 1.75 g/cm 3 to 1.95 g/cm 3 .

8. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a NO 3 :U ratio of 1.5 to 1.9; a uranium concentration of from 0.5 M to 3.5 M; and a pH of 0.5 to 2.8.

9. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a NO 3 :U ratio of 1.5 to 1.7; a uranium concentration of from 0.5 M to 3.5 M; and a pH of 0.8 to 2.8.

10. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a NO 3 :U ratio of 1.5 to 1.9; a uranium concentration of from 2.5 M to 3.0 M; and a pH of less than 1.8.

11. The method of claim 1 , wherein the acid deficient uranyl nitrate solution has a NO 3 :U ratio of 1.5 to 1.7; a uranium concentration of from 2.5 M to 3.0 M; and a pH of 1.2 to 1.8.

12. The method of claim 1 , wherein the uranium solution is maintained at the desired temperature under a pressure of from 20 to 50 atmospheres for a desired hold time, wherein the desired temperature is between 200° C. and 250° C.

13. The method of claim 1 , wherein the uranium solution is maintained at the desired temperature under a pressure of from 20 to 50 atmospheres for a desired hold time, wherein the desired temperature is between 215° C. and 240° C.

14. The method of claim 13 , wherein the desired hold time is 15 min to 6 hours.

15. The method of claim 13 , wherein the desired hold time is 30 min to 2 hours.

16. The method of claim 1 , wherein the desired temperature is reduced to between 30° C. and 90° C. before reducing the pressure on the uranium solution to atmospheric pressure.

17. A method of preparing a solution of acid deficient uranyl nitrate having a formula of UO 2 (OH) y (NO 3 ) 2-y , where y ranges from 0.1 to 0.5, the method comprising:

a) dissolving UO 2 (NO 3 ) 2 or a hydrate thereof in aqueous nitric acid to produce a uranium solution;

b) placing the uranium solution under a pressure greater than atmospheric pressure in a sealed reaction chamber;

c) heating the uranium solution to a desired temperature of between 150° C. and 250° C. by applying microwave energy to the uranium solution;

d) maintaining the uranium solution at the desired temperature under elevated pressure for a desired hold time;

e) partially venting the pressure on the uranium solution without allowing the uranium solution to boil; and

f) reducing the desired temperature to below 100° C. and reducing the pressure on the uranium solution to atmospheric pressure to obtain an acid deficient uranyl nitrate solution.

18. A method of preparing a solution of acid deficient uranyl nitrate having a formula of UO 2 (OH) y (NO 3 ) 2-y , where y ranges from 0.1 to 0.5, the method comprising:

a) dissolving U x O z in aqueous nitric acid to produce a uranium solution, wherein x is 1 to 3 and z is 2 to 8;

b) placing the uranium solution under a pressure under a pressure of from 20 to 50 atmospheres in a sealed reaction chamber;

c) heating the uranium solution by applying microwave energy to the uranium solution;

d) maintaining the uranium solution at the desired temperature under elevated pressure for a desired hold time of between 15 min and 6 hours;

e) partially venting the pressure on the uranium solution without allowing the uranium solution to boil; and

f) reducing the desired temperature to below 100° C. and reducing the pressure on the uranium solution to atmospheric pressure to obtain an acid deficient uranyl nitrate solution.

19. The method of claim 18 , wherein the step of heating the uranium solution comprises heating the uranium solution to a temperature of between 150° C. and 250° C. by applying microwave energy to the uranium solution.

Assignments (8)
RELEASE OF SECURITY INTEREST Recorded Feb 13, 2026
From: LIVE OAK BANKING COMPANY
To: X-ENERGY
Reel/Frame 073783/0139 →
SECURITY INTEREST Recorded May 12, 2025
From: X-ENERGY, LLC
To: LIVE OAK BANKING COMPANY
Reel/Frame 071081/0865 →
RELEASE OF SECURITY INTEREST Recorded Feb 4, 2025
From: ARES ACQUISITION HOLDINGS LP
To: X-ENERGY, LLC
Reel/Frame 070107/0678 →
RELEASE OF SECURITY INTEREST Recorded Oct 14, 2024
From: ARES ACQUISITION HOLDINGS LP
To: X-ENERGY, LLC
Reel/Frame 068884/0531 →
RELEASE OF INTELLECTUAL PROPERTY SECURITY INTEREST, RECORDED AT REEL/FRAME 068722/0427 Recorded Oct 11, 2024
From: AMAZON.COM NV INVESTMENT HOLDINGS, LLC
To: X-ENERGY, LLC
Reel/Frame 069717/0581 →
SECURITY INTEREST Recorded Sep 27, 2024
From: X-ENERGY, LLC
To: AMAZON.COM NV INVESTMENT HOLDINGS LLC
Reel/Frame 068722/0427 →
SECURITY INTEREST Recorded Oct 10, 2023
From: X-ENERGY, LLC
To: ARES ACQUISITION HOLDINGS LP
Reel/Frame 065174/0313 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2020
From: BROWN, DANIEL; LINNEEN, NICHOLAS
To: X ENERGY, LLC
Reel/Frame 054268/0742 →
Continuity (2)
Provisional Application 62930172 · Nov 4, 2019
Related Publication 20210130181A1 · May 6, 2021