IP Library Granted Patent US 10,808,064
Granted Patent B2
US 10,808,064 · App. 15/770,352 · Granted Oct 20, 2020

Amphiphilic block polymers soluble in strongly saline medium

Inventors: David James Wilson (Coye la Foret, FR); Mikel Morvan (Pessac, FR); Max Chabert (Ivry-sur-Seine, FR); Arnaud Cadix (Saint-Ouen, FR)
Assignee: RHODIA OPERATIONS
C08F293/005C09K8/588C09K8/68C08F212/08C08F220/1812C08F2438/03
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Quick Facts
Patent No.
US 10,808,064
App. No.
15/770,352
Granted
Oct 20, 2020
Kind
B2
Abstract

The present invention relates to the preparation of polymers that are of use in particular as a rheology agent, and are suitable for use in very concentrated saline media, which comprises a step of micellar radical polymerization in which are brought into contact, in an aqueous medium: —hydrophilic monomers; —hydrophobic monomers in the form of a micellar solution, containing micelles comprising these hydrophobic monomers; —a radical polymerization initiator; and —preferably an agent for controlling radical polymerization, wherein said micelles comprise at least one surfactant of amphoteric nature. The polymers obtained according to the invention are in particular of use for enhanced oil recovery.

Claims (47)

1. A process for preparing a block copolymer, the process comprising a step (E) of micellar radical polymerization comprising placing the following in contact, in an aqueous medium (M):

hydrophilic monomers, dissolved or dispersed in said aqueous medium (M);

hydrophobic monomers in the form of a micellar solution containing, in dispersed form in the aqueous medium (M), micelles comprising the hydrophobic monomers, wherein the hydrophobic monomers comprise t-butylstyrene;

at least one radical polymerization initiator,

wherein said micelles comprise at least one surfactant of amphoteric nature.

2. The process as claimed in claim 1 , wherein the amphoteric surfactant is selected from the group consisting of:

betaines;

sulfobetaines;

alkylamphoacetates and alkylamphodiacetates;

alkylamphopropionates or alkylamphodipropionates;

alkyl amphohydroxypropyl sultaines;

iminopropinates;

alkyl amine oxides; and

mixtures of surfactants comprising one or more of the abovementioned compounds.

3. The process as claimed in claim 2 , wherein the amphoteric surfactant is selected from the group consisting of:

cetyl betaine;

sulfobetaines;

alkylamphoacetates and alkylamphodiacetates;

alkylamphopropionates or alkylamphodipropionates;

alkyl amphohydroxypropyl sultaines;

iminopropionates;

lauramine oxide; and

mixtures of surfactants comprising one or more of the abovementioned compounds.

4. The process as claimed in claim 1 , wherein the hydrophobic monomers of step (E) comprise a C 1 -C 30 alkyl α,β-unsaturated ester.

5. The process as claimed in claim 4 , wherein the hydrophobic monomers of step (E) comprise a C 4 -C 22 alkyl α,β-unsaturated ester.

6. The process as claimed in claim 5 , wherein the hydrophobic monomers of step (E) comprise lauryl methacrylate.

7. The process according to claim 1 , wherein the at least one radical polymerization initiator is water-soluble or water-dispersible.

8. The process according to claim 1 , comprising placing the following in contact, in the aqueous medium (M):

hydrophilic monomers, dissolved or dispersed in said aqueous medium (M);

hydrophobic monomers in the form of a micellar solution;

at least one radical polymerization initiator, and

at least one radical polymerization control agent, wherein said micelles comprise at least one surfactant of amphoteric nature.

9. The process as claimed in claim 8 , wherein the radical polymerization control agent is a compound which comprises a thiocarbonylthio —S(C═S)— group.

10. The process according to claim 9 , wherein the thiocarbonylthio —S(C═S)— group is a xanthate.

11. The process as claimed in claim 8 , wherein the radical polymerization control agent is an oligomer which is of water-soluble or water-dispersible nature bearing a thiocarbonylthio —S(C═S)— group and which

is soluble or dispersible in the aqueous medium (M) used in step (E); and/or

is not suitable for penetrating into the micelles of the micellar solution.

12. The process as claimed in claim 11 , wherein the radical polymerization control agent is a prepolymer bearing at least one thiocarbonylthio —S(C═S)— group obtained on conclusion of a step (E 0 ), prior to step (E), said step (E 0 ) comprising placing in contact

hydrophilic monomers;

a radical polymerization initiator; and

a control agent bearing a thiocarbonylthio group —S(C═S)—.

13. The process according to claim 12 , wherein the hydrophilic monomers of step (E 0 ) are identical to those of step (E).

14. A polymer composition obtained according to the process of claim 1 .

15. A method comprising regulating rheology of a liquid medium by dissolving in the liquid medium the polymer composition or the polymer contained in the polymer composition as claimed in claim 14 .

16. The method as claimed in claim 15 , wherein said polymer composition is dissolved in an aqueous medium comprising more than 50 g/l of salt.

17. The method according to claim 15 , wherein the liquid medium is an aqueous medium.

18. The method according to claim 17 , wherein the aqueous medium is for oil or natural gas extraction.

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 May 29, 2018
From: WILSON, DAVID JAMES; MORVAN, MIKEL; CHABERT, MAX; CADIX, ARNAUD
To: RHODIA OPERATIONS
Reel/Frame 045923/0028 →