IP Library Granted Patent US 11,608,391
Granted Patent B2
US 11,608,391 · App. 17/257,839 · Granted Mar 21, 2023

Progressive salting-out of polymer chains in a liquid medium

Inventors: Dominique Labarre (Neuilly sur Seine, FR); David James Wilson (Coye-la-Foret, FR)
Assignee: RHODIA OPERATIONS
C08F2/22C08F293/005C09K8/528C09K8/54C08F220/1812C08F2438/03C09K2208/22C09K2208/32
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Quick Facts
Patent No.
US 11,608,391
App. No.
17/257,839
Granted
Mar 21, 2023
Kind
B2
Abstract

Provided is a method making it possible to ensure a gradual release of polymer chains within a liquid medium, the method comprising bringing the liquid medium into contact with specific solid objects formed by polymer chains soluble in the medium and carrying hydrophobic side groups ensuring physical crosslinking between the polymer chains within the solid objects. The released chains may in particular be used as inhibitors of the formation of inorganic or organic deposits (scale inhibitors) within a liquid medium, typically in the field of oil extraction.

Claims (21)

1. A method for the gradual release of polymer chains within a liquid release medium (LRM), said method comprising a step (S) comprising contacting said medium (LRM) with solid objects, wherein the solid objects are formed by polymer chains soluble in the medium (LRM) and carrying hydrophobic side groups ensuring hydrophobic/hydrophobic physical crosslinking between said polymer chains within said solid objects, and

wherein the solid objects employed in step (S) result from a step (S0) of micellar radical polymerization in which the following are brought into contact, within an aqueous medium (M):

ethylenically unsaturated monomers (m1), dissolved or dispersed in said aqueous medium (M);

ethylenically unsaturated monomers (m2), in the form of a micellar solution, namely containing, in the dispersed state within the medium (M), micelles comprising these hydrophobic monomers, said monomers (m2) being, in all or part, monomers carrying hydrophobic chains suitable for ensuring the desired hydrophobic/hydrophobic physical crosslinking in the solid objects employed in step (S);

at least one radical polymerization initiator; and

at least one radical polymerization control agent, and

wherein the monomers employed in step (S0) contain crosslinking monomers (mR) comprising at least two ethylenic unsaturations separated by at least one cleavable group, and

wherein the molar ratio (mR)/(m1), which corresponds to the amount of crosslinking monomers (mR) with respect to the total amount of hydrophilic monomers, is greater than 0.5% and less than or equal to 30%.

2. The method as claimed in claim 1 , wherein the released polymer chains have a number average molecular weight of between 500 and 100 000 g/mol.

3. The method as claimed in claim 1 , wherein the medium (LRM) is an aqueous medium and wherein the released polymer chains are water-soluble.

4. The method as claimed in claim 1 , wherein the radical polymerization control agent is a compound which comprises a thiocarbonylthio —S(C═S)— group.

5. The method as claimed in claim 1 , wherein the polymer chains released are polymer chains useful as scale-inhibiting, clathrate-inhibiting and/or corrosion-inhibiting agent.

6. The method as claimed in claim 5 , wherein the medium (LRM) of step (S) is a liquid medium encountered during the extraction of oil within a hydrocarbon reservoir.

7. The method as claimed in claim 1 , where step (S) is carried out at a temperature of greater than or equal to 50° C., and of less than or equal to 150° C.

8. The method as claimed in claim 1 , wherein the at least one radical polymerization initiator is water-soluble or water-dispersible.

9. The method as claimed in claim 1 , wherein the radical polymerization control agent is a xanthate.

10. The method as claimed in claim 1 , wherein the molar ratio (mR)/(m1), which corresponds to the amount of crosslinking monomers (mR) with respect to the total amount of hydrophilic monomers, is greater than 1% and less than or equal to 30%.

11. The method as claimed in claim 1 , wherein the molar ratio (mR)/(m1), which corresponds to the amount of crosslinking monomers (mR) with respect to the total amount of hydrophilic monomers, is greater than 2% and less than or equal to 30%.

12. The method as claimed in claim 1 , wherein the molar ratio (mR)/(m1), which corresponds to the amount of crosslinking monomers (mR) with respect to the total amount of hydrophilic monomers, is less than or equal to 20%.

13. The method as claimed in claim 1 , wherein the molar ratio (mR)/(m1), which corresponds to the amount of crosslinking monomers (mR) with respect to the total amount of hydrophilic monomers, is less than or equal to 10%.

14. The method as claimed in claim 1 , where step (S) is carried out at a temperature between 60° C. and 120° C.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2023
From: RHODIA OPERATIONS
To: ENERGY SOLUTIONS (US) LLC
Reel/Frame 063149/0540 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 21, 2021
From: LABARRE, DOMINIQUE; WILSON, DAVID JAMES
To: RHODIA OPERATIONS
Reel/Frame 054988/0146 →
Cited By (1)
US 12,448,560