IP Library Granted Patent US 12,655,027
Granted Patent B2
US 12,655,027 · App. 18/194,362 · Granted Jun 16, 2026

Composite ammonium diuranate gel particles with a phenolic resin phase, and methods of making the same

Inventor: Nick Lineen (Knoxville, TN)
Assignee: X-ENERGY, LLC
C01B32/907C01B32/928C08G8/10C08K5/0091G21C3/623C01P2006/44
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Quick Facts
Patent No.
US 12,655,027
App. No.
18/194,362
Granted
Jun 16, 2026
Kind
B2
Abstract

Composite gel particles with an ammonium diuranate matrix phase and a phenolic resin phase incorporated within the ammonium diuranate matrix phase are produced from a first solution comprising uranyl nitrate, a phenol, and optionally formaldehyde, wherein the uranyl nitrate and the phenol are present in a ratio ranging from 2:1 to 25:1; and a second solution comprising hexamethylenetetramine and urea. The first solution and the second solution are mixed, and drops of the resulting mixture into a heated second liquid which is immiscible with the mixed solution. Heat from the second liquid causes the hexamethylenetetramine to decompose to form ammonia, which reacts with the uranyl nitrate to cause each of the drops to form an ammonium diuranate gel particle. The ammonium diuranate gel particles are collected. The ammonium diuranate gel particles include the phenolic resin phase within the ammonium diuranate matrix phase, where the phenolic resin phase is formed by reaction between the phenol and formaldehyde. The first solution may include uranyl nitrate, the phenol, and formaldehyde, and the formaldehyde and the phenol may react to form the phenolic resin phase prior to mixing the first solution and the second solution. The first solution may be free of formaldehyde, and heat from the second liquid may causes the hexamethylenetetramine to decompose to form formaldehyde in situ; so that the formaldehyde and the phenol react to form the phenolic resin phase while the ammonia reacts with the uranyl nitrate.

Claims (45)

1 . A method of making composite gel particles comprising an ammonium diuranate matrix phase and a phenolic resin phase incorporated within the ammonium diuranate matrix phase, comprising:

preparing a first solution comprising uranyl nitrate, a phenol, and optionally formaldehyde in a first portion of a first liquid carrier, wherein the uranyl nitrate and the phenol are present in a mole ratio ranging from 2:1 to 25:1;

preparing a second solution comprising hexamethylenetetramine and urea in a second portion of the first liquid carrier;

mixing the first solution and the second solution to form a mixture;

adding individual drops of the mixture into a heated second liquid, wherein:

the first liquid carrier is immiscible in the second liquid;

heat from the second liquid causes the hexamethylenetetramine to decompose to form ammonia; and

the ammonia reacts with the uranyl nitrate to cause each of the individual drops to form an ammonium diuranate gel particle; and

collecting the ammonium diuranate gel particles formed from the individual drops of the mixture;

wherein the ammonium diuranate gel particles comprise the phenolic resin phase within the ammonium diuranate matrix phase;

wherein the phenolic resin phase is formed by reaction between the phenol and formaldehyde.

2 . The method of claim 1 , wherein:

the first solution comprises uranyl nitrate, the phenol, and formaldehyde,

the formaldehyde and the phenol are present in the first solution in a mole ratio ranging from 1:1 to 5:1; and

the formaldehyde and the phenol react to form the phenolic resin phase prior to mixing the first solution and the second solution.

3 . The method of claim 2 , wherein:

the phenolic resin phase forms as small particles of a phenolic resin suspended within the first solution;

the ammonium diuranate gel particles comprise the small particles of a phenolic resin within the ammonium diuranate matrix phase.

4 . The method of claim 1 , wherein:

the first solution does not include formaldehyde,

heat from the second liquid causes the hexamethylenetetramine to decompose to form ammonia and formaldehyde in situ; and

the formaldehyde and the phenol react to form the phenolic resin phase while the ammonia reacts with the uranyl nitrate.

5 . The method of claim 1 , wherein the phenol is selected from the group consisting of phenol, benzenediols, phenols substituted with a C1-C4 alkyl group, benzenediols substituted with a C1-C4 alkyl group, and mixtures thereof.

6 . The method of claim 1 , wherein the phenol is selected from the group consisting of phenol, catechol, resorcinol, hydroquinone, 2-methylphenol, 3-methylphenol, 4-methylphenol, 2,3-dihydroxytoluene, 3,4-dihydroxytoluene, 2-methylbenzene-1,3-diol, 4-methylbenzene-1,3-diol, dihydroxytoluene, 2-methylbenzene-1,4-diol, 3-methylbenzene-1,4-diol, and mixtures thereof.

7 . The method of claim 6 , wherein the phenol is phenol, catechol, resorcinol, 2-methylphenol, 3-methylphenol, 4-methylphenol, or a mixture thereof.

8 . The method of claim 7 , wherein the phenol is resorcinol.

9 . The method of claim 1 , wherein:

the first liquid carrier is water or a aqueous solution, and

the second liquid is a water-immiscible organic phase.

10 . The method of claim 9 , wherein the water-immiscible organic phase is a silicone oil or a hydrocarbon oil.

11 . A method of making composite gel particles comprising an ammonium diuranate matrix phase and phenolic resin particles incorporated within the ammonium diuranate matrix phase, comprising:

preparing a uranyl nitrate solution comprising uranyl nitrate, a phenol, and a C1-C4 aldehyde in a first portion of a first liquid carrier, wherein the uranyl nitrate and the phenol are present in a mole ratio ranging from 2:1 to 25:1;

preparing a second solution comprising hexamethylenetetramine and urea in a second portion of the first liquid carrier;

reacting the phenol and the C1-C4 aldehyde in the uranyl nitrate solution to produce the phenolic resin particles suspended in the uranyl nitrate solution;

mixing the uranyl nitrate solution with the phenolic resin particles therein and the second solution to form a mixture;

adding individual drops of the mixture into a heated second liquid, wherein:

the first liquid carrier is immiscible in the second liquid;

heat from the second liquid causes the hexamethylenetetramine to decompose to form ammonia; and

the ammonia reacts with the uranyl nitrate to cause each of the individual drops to form an ammonium diuranate gel particle; and

collecting the ammonium diuranate gel particles formed from the individual drops of the mixture;

wherein the ammonium diuranate gel particles comprise the phenolic resin particles within the ammonium diuranate matrix phase.

12 . The method of claim 11 , wherein the phenol is selected from the group consisting of phenol, catechol, resorcinol, hydroquinone, 2-methylphenol, 3-methylphenol, 4-methylphenol, 2,3-dihydroxytoluene, 3,4-dihydroxytoluene, 2-methylbenzene-1,3-diol, 4-methylbenzene-1,3-diol, dihydroxytoluene, 2-methylbenzene-1,4-diol, 3-methylbenzene-1,4-diol, and mixtures thereof.

13 . The method of claim 11 , wherein the C1-C4 aldehyde is:

selected from the group consisting of formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, isobutyraldehyde, and a mixture thereof; or

produced by depolymerization of 1,3,5-trioxane or 2,4,6-trimethyl-1,3,5-trioxane.

Assignments (3)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2023
From: LINEEN, NICK
To: X-ENERGY, LLC
Reel/Frame 063195/0467 →
Continuity (1)
Related Publication 20240327226A1 · Oct 3, 2024
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