IP Library Granted Patent US 9,574,022
Granted Patent B2
US 9,574,022 · App. 13/876,434 · Granted Feb 21, 2017

Controlled free-radical polymerization of N-vinyl lactams in an aqueous medium

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Quick Facts
Patent No.
US 9,574,022
App. No.
13/876,434
Granted
Feb 21, 2017
Kind
B2
Abstract

The present invention relates to a method for preparing a polymer based on N-vinyl lactam monomer units, which comprises a step (E) for controlled radical polymerization of a composition comprising: monomers containing (and most often consisting of) N-vinyl lactam monomers, either identical or different (and generally identical); an agent for controlling the radical polymerization, for example comprising a thiocarbonylthio group —S(C═S)—; and a radical polymerization initiator which is a redox system comprising a reducing agent (Red) and an oxidizing agent (Ox).

Claims (25)

1. A method for preparing a polymer based on N-vinyl lactam monomer units, which comprises a controlled radical polymerization step (E) for a composition comprising:

monomers containing N-vinyl lactam monomers either identical or different; and

a control agent for the radical polymerization; and

a radical polymerization initiator which is a redox system, comprising a reducing agent and an oxidizing agent, wherein the difference between the standard redox potentials of the oxidizer and of the reducing agent (E ox -E red ) is of at least 1V;

wherein the control agent is a compound bearing a xanthate function —S(C═S)O—.

2. The method according to claim 1 , wherein step (E) is conducted in an aqueous medium.

3. The method according to claim 1 , wherein the difference between the standard redox potentials of the oxidizer and of the reducing agent (E ox -E red ) is of at least 1.2V.

4. The method according to claim 1 , wherein the control agent is O-ethyl-S-(1-methoxycarbonyl ethyl) xanthate of formula (CH 3 CH(CO 2 CH 3 ))S(C═S)OCH 2 CH 3 ).

5. The method according to claim 1 , wherein, in step (E), the N-vinyl lactam monomers are N-vinylpyrrolidone monomers (NVP).

6. The method according to claim 1 , wherein step (E) is conducted at a temperature below 40° C.

7. The method according to claim 6 , wherein step (E) is conducted at room temperature.

8. The method according to claim 1 , wherein the oxidation standard redox potential Eox of the oxidizing agent applied in step (E) is less than that of the N-vinyl lactam monomers used.

9. The method according to claim 8 , wherein, in step (E), the oxidizing agent used is tertbutyl hydroperoxide (t-BuOOH).

10. The method according to claim 1 , wherein, in step (E), the reducing and oxidizing agents have a pKa of more than 4.

11. The method according to claim 1 , wherein, in step (E), the reducing agent is sodium sulfite.

12. The method according to claim 1 , wherein, in step (E), the reducing agent is ascorbic acid.

13. The method according to claim 1 , wherein, in step (E), the oxidizing agent used is tertbutyl hydroperoxide (t-BuOOH) and the reducing agent is sodium sulfite.

14. The method according to claim 1 , wherein, in step (E), the oxidizing agent used is tertbutyl hydroperoxide (t-BuOOH) and the reducing agent is ascorbic acid.

15. The method according to claim 1 , for the synthesis of sequenced copolymers, which includes, after step (E), a step (E1) for controlled radical polymerization of a mixture comprising:

all or part of the polymer as obtained at the end of step (E);

ethylenically unsaturated monomers; and

a source of free radicals.

16. The method according to claim 1 , wherein the control agent is a compound bearing an —O-ethyl xanthate function of formula —S(C═S)OCH 2 CH 3 .

17. The method according to claim 1 , wherein the reducing agent and the oxidizing agent are separately introduced into the medium of step (E).

18. The method according to claim 1 , wherein step (E) is conducted (i) first by forming a mixture comprising one of the oxidizing or reducing agents in a mixture with the monomers and the control agents and then (ii) by adding to this mixture the other of the oxidizing or reducing agents.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 26, 2024
From: RHODIA OPERATIONS
To: SPECIALTY OPERATIONS FRANCE
Reel/Frame 066374/0642 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2023
From: RHODIA OPERATIONS
To: SPECIALTY OPERATIONS FRANCE
Reel/Frame 065488/0365 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2013
From: DESTARAC, MATHIAS; GUINAUDEAU, AYMERIC; MAZIERES, STEPHANE; WILSON, JAMES
To: RHODIA OPERATIONS; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S)
Reel/Frame 031507/0654 →