IP Library Granted Patent US 8,912,296
Granted Patent B1
US 8,912,296 · App. 14/366,803 · Granted Dec 16, 2014

Process for preparing polystyrene having a high melt flow rate

Inventors: Gilbert Bouquet (Ghent, BE); Ulrich Reifert (Halle, DE); Nicolaas M. A. Hermans (Terneuzen, NL)
Assignee: Styron Europe GmbH
C08F112/08C08J9/16C08J9/228C08J2325/06
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Quick Facts
Patent No.
US 8,912,296
App. No.
14/366,803
Granted
Dec 16, 2014
Kind
B1
Abstract

Provided is a process for preparing polystyrene having a weight average molecular weight (Mw) in the range of 120,000-160,000 g/mol, a polydispersity in the range of 4-6 and a melt flow rate of at least 40 g/10 minutes by feeding styrene into a reaction system through which the styrene passes as a component of a reaction mixture as it is polymerized, the reaction system including an initial reaction zone ( 100 ) and a downstream reaction zone ( 200 ), comprising the steps of: polymerizing styrene in the initial reaction zone to form polystyrene having a Mw of greater than 300,000 g/mol and a polydispersity in the range 1.5-2.5, 10-30 wt. % of the styrene fed to the initial reaction zone being polymerized there, —and polymerizing styrene remaining in the reaction mixture in the downstream reaction zone, a chain transfer agent being mixed with the reaction mixture at the commencement of this reaction zone and optionally at one or more additional locations within this reaction zone. The polystyrene may be used to manufacture expandable polystyrene beads or polystyrene foam board.

Claims (26)

1. A process for preparing polystyrene having a weight average molecular weight (Mw) in the range of 120,000-160,000, a polydispersity in the range of 4-6 and a melt flow rate of a least 40 g/10 minutes by feeding styrene into a reaction system through which the styrene passes as a component of a reaction mixture as it is polymerized, the reaction system including an initial reaction zone and a downstream reaction zone, comprising the steps of: polymerizing styrene in the initial reaction zone to form polystyrene having a Mw of greater than 300,000 and a polydispersity in the range of 1.5- to 2.5, 10- to 30 wt. % of the styrene fed to the initial reaction zone being polymerized there; and polymerizing styrene remaining in the reaction mixture in the downstream reaction zone, a chain transfer agent being mixed with the reaction mixture at the commencement of the downstream reaction zone.

2. A process according to claim 1 , wherein the temperature of the reaction mixture in the initial reaction zone is 120-135° C. and the temperature of the reaction mixture in the downstream reaction zone is 135-190° C.

3. A process according to claim 1 , wherein the styrene feed fed to the initial reaction zone comprises 2-8 wt. % of an organic solvent.

4. A process according to claim 3 , wherein the solvent is ethylbenzene.

5. A process according to claim 1 , wherein the cumulative concentration of chain transfer agent in the reaction mixture in the downstream reaction zone is 3000-6000 ppm.

6. A process according claim 1 , wherein the downstream reaction zone includes multiple sub-zones including a zone Z1 where the chain transfer agent is added into the reaction mixture and where the temperature of the reaction mixture is 136-158° C. and a zone Z2 downstream of Z1 where no chain transfer agent is added and where the temperature of the reaction mixture is 159-190° C.

7. A process according to claim 1 , including separating polystyrene having a Mw in the range of 120,000-160,000, a polydispersity in the range of 4-6 and a melt flow rate of at least 40 g/10 minutes from the reaction mixture exiting the downstream reaction zone and recycling at least a portion of the remainder of the reaction mixture.

8. A process according to claim 7 , wherein 15-30% by weight of the reaction mixture exiting the downstream reaction zone is recycled.

9. A process according to claim 7 , wherein no chain transfer agent is added to the initial reaction zone apart from any residual chain transfer agent which might be present in the reaction mixture recycled from the downstream reaction zone.

10. A process according to claim 7 , wherein the polystyrene separated from the reaction mixture has a number average molecular weight (Mn) of 28,000-38,000.

11. A process according to claim 7 , wherein the polystyrene separated from the reaction mixture is molten.

12. A process for manufacturing expandable polystyrene beads comprising the steps of:

(i) preparing polystyrene by a method according to claim 11 , (ii) feeding the molten polystyrene separated from the reaction mixture into an extruder where it is mixed with a blowing agent and extruding the mixture, and (iii) cutting the extruded mixture of polystyrene and blowing agent into polystyrene beads.

13. A process for manufacturing a polystyrene foam board comprising the steps of;

ii) preparing polystyrene by a method according to claim 11 ,

(ii) feeding the molten polystyrene separated from the reaction mixture into an extruder where it is mixed with a blowing agent, and

(iii) extruding the mixture of polystyrene and blowing agent to manufacture the polystyrene foam board.

14. A process according to claim 7 , wherein the polystyrene separated from the reaction mixture is formed into pellets.

15. A process for manufacturing expandable polystyrene beads comprising the steps of:

(i) preparing polystyrene pellets in accordance with the process of claim 14 ,

(ix) feeding the polystyrene pellets into an extruder where they are mixed with a blowing agent and extruding the mixture, and

(iii) cutting the extruded mixture of polystyrene and blowing agent into polystyrene beads.

16. A process for manufacturing a polystyrene foam board comprising the steps of:

(i) preparing polystyrene pellets in accordance with the process of claim 14 ,

(ii) feeding the polystyrene pellets into an extruder where they are mixed with a blowing agent, and (iii) extruding the mixture of polystyrene and blowing agent to manufacture the polystyrene foam board.

17. A process according to claim 1 wherein in the chain transfer agent is mixed at the commencement of the downstream reaction zone and at one or more additional locations within the downstream reaction zone.

Assignments (6)
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT REEL 036303, FRAME 0749 Recorded Sep 6, 2017
From: DEUTSCHE BANK AG NEW YORK BRANCH
To: TRINSEO EUROPE GMBH
Reel/Frame 043773/0059 →
PATENT SECURITY AGREEMENT Recorded Sep 6, 2017
From: TRINSEO EUROPE GMBH
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
Reel/Frame 043773/0138 →
PATENT SECURITY AGREEMENT Recorded Aug 6, 2015
From: TRINSEO EUROPE GMBH
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
Reel/Frame 036303/0749 →
CHANGE OF NAME Recorded Jun 25, 2015
From: STYRON EUROPE GMBH
To: TRINSEO EUROPE GMBH
Reel/Frame 036024/0806 →
CHANGE OF NAME Recorded Jun 12, 2015
From: STYRON EUROPE GMBH
To: TRINSEO EUROPE GMBH
Reel/Frame 036007/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2014
From: BOUQUET, GILBERT; HERMANS, NICOLAAS M.A.; REIFERT, ULRICH
To: STYRON EUROPE GMBH
Reel/Frame 033138/0982 →
Priority Claims (1)
GB 1122017.5 · Dec 20, 2011 · national