IP Library Granted Patent US 8,987,391
Granted Patent B2
US 8,987,391 · App. 13/704,676 · Granted Mar 24, 2015

Polymerization process with in-situ initiator formation

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Quick Facts
Patent No.
US 8,987,391
App. No.
13/704,676
Granted
Mar 24, 2015
Kind
B2
Abstract

A process for the polymerization of one or more monomers wherein at least one anhydride and at least one peroxy compound selected from inorganic peroxides, organic hydroperoxides, and peroxyacids are dosed during the polymerization reaction in a continuous or intermittent fashion to a reaction mixture comprising said monomers.

Claims (23)

1. A process for the polymerization of one or more monomers wherein at least one anhydride and at least one peroxy compound chosen from inorganic peroxides, organic hydroperoxides, and peroxyacids are dosed during the polymerization reaction in a continuous or intermittent fashion to a reaction mixture comprising said monomers,

wherein at least 50 wt % of the one or more monomers is vinyl chloride.

2. The process according to claim 1 wherein the peroxy compound is hydrogen peroxide.

3. The process according to claim 1 wherein peroxy compound is a peroxyacid is selected from the group consisting of peracetic acid, perpropionic acid, perisobutyric acid, perpivalic peracid, perisononanoic peracid, and ethylbutanoic peracid.

4. The process according to claim 1 wherein the anhydride is selected from the group consisting of isobutyric anhydride, acetic anhydride, pivalic anhydride, isovaleric anhydride, neodecanoic anhydride, neoheptanoic anhydride, and 2-ethyl hexanoic anhydride.

5. The process according to claim 1 wherein the peroxy compound and the anhydride are dosed to the reaction mixture at at least 2 moments during the polymerization reaction.

6. The process according to claim 1 wherein the peroxy compound and the anhydride are dosed via separate dosing lines.

7. The process according to claim 1 wherein the peroxy compound and the anhydride are dosed via the same dosing line.

8. The process according to claim 1 wherein the peroxy compound and/or the anhydride is/are dosed using a dosing line containing a static mixer.

9. The process according to claim 2 wherein the reaction mixture during the polymerization reaction contains a molar excess of hydrogen peroxide relative to anhydride.

10. The process according to claim 1 wherein at least 5 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 10 wt % of all monomers has been converted.

11. The process according to claim 1 wherein the anhydride concentration in the reaction mixture does not exceed 3000 ppm, based on the total weight of the reaction mixture, during the entire process.

12. The process according to claim 1 wherein the peroxy compound concentration in the reaction mixture does not exceed 500 ppm, based on the total weight of the reaction mixture, during the entire process.

13. The process according to claim 1 wherein the peroxy compound and the anhydride are dosed to the reaction mixture at at least 4 moments during the polymerization reaction.

14. The process according to claim 1 wherein the peroxy compound and the anhydride are dosed to the reaction mixture at at least 10 moments during the polymerization reaction.

15. The process according to claim 1 wherein the peroxy compound and the anhydride are dosed to the reaction mixture at at least 20 moments during the polymerization reaction.

16. The process according to claim 1 wherein at least 10 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 10 wt % of all monomers has been converted.

17. The process according to claim 1 wherein at least 20 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 10 wt % of all monomers has been converted.

18. The process according to claim 1 wherein at least 50 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 10 wt % of all monomers has been converted.

19. The process according to claim 1 wherein at least 5 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 30 wt % of all monomers has been converted.

20. The process according to claim 1 wherein at least 10 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 30 wt % of all monomers has been converted.

21. The process according to claim 1 wherein at least 20 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 30 wt % of all monomers has been converted.

22. The process according to claim 1 wherein at least 50 wt % of the total amount of peroxy compound and anhydride to be dosed during the process is dosed to the reaction mixture after at least 30 wt % of all monomers has been converted.

Assignments (4)
CHANGE OF NAME Recorded Sep 18, 2019
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050426/0671 →
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
CHANGE OF ADDRESS Recorded May 15, 2017
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 042745/0406 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 19, 2013
From: GERRITSEN, RENE; SCHUT, JACOBUS; OVERKAMP, JOHANNES WILLIBRORDUS ANTONIUS; DE JONG, JOHANNES JACOBUS THEODORUS
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 029828/0028 →