IP Library Granted Patent US 7,737,229
Granted Patent B2
US 7,737,229 · App. 10/577,695 · Granted Jun 15, 2010

Continuous preparation of ethylene homopolymers or copolymers

Assignee: Basell Polyolefine GmbH
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Quick Facts
Patent No.
US 7,737,229
App. No.
10/577,695
Granted
Jun 15, 2010
Kind
B2
Abstract

The invention relates to a process for the continuous preparation of ethylene homopolymers or copolymers in the presence of free-radical polymerization initiators and, if desired, molecular weight regulators at from 120° C. to 350° C. and pressures in the range from 100 to 4000 bar, in which the polymer is separated from unpolymerized ethylene in a high-pressure stage at a pressure of from 100 to 500 bar and at least one low-pressure stage at a pressure of from 1 to 100 bar and the ethylene separated off in the high-pressure stage is separated from remaining monomeric, oligomeric and/or polymeric constituents and recirculated to the inlet of the tube reactor in a high-pressure circuit and the ethylene separated off in the low-pressure stage is separated from remaining monomeric, oligomeric and/or polymeric constituents and recirculated to the inlet of the tube reactor in a low-pressure circuit. The initiator is used as a solution in an isoparaffinic solvent having a boiling point of not more than 160° C. and the solvent is separated from the other monomeric, oligomeric and/or polymeric constituents in the low-pressure circuit. The solvent is then, if appropriate after being admixed with fresh solvent, reused for dissolving initiator.

Claims (10)

1. A process for continuously preparing an ethylene homopolymer or copolymer in a high-pressure tube reactor in presence of at least one free-radical polymerization initiator and, optionally, a least one molecular weight regulator at from 120° C. to 350° C. and a pressure from 1000 to 4000 bar, wherein the ethylene homopolymer or copolymer is separated from unpolymerized ethylene and optionally from comonomers in a high-pressure stage at a pressure from 100 to 500 bar and at least one low-pressure stage at a pressure from 1 to 100 bar, the unpolymerized ethylene separated off in the high-pressure stage is separated from any remaining monomeric, oligomeric and/or polymeric constituents and is re-circulated to a first inlet of the tube reactor in a high-pressure circuit, and the unpolymerized ethylene separated off in the low-pressure stage is separated from any remaining monomeric, oligomeric and/or polymeric constituents and is re-circulated to a second inlet of the tube reactor in a low-pressure circuit, wherein the free-radical polymerization initiator is used as a solution in an isoparaffinic solvent, the isoparaffinic solvent comprising a boiling point equal to or less than 160° C., and the isoparaffinic solvent is separated from the monomeric, oligomeric and/or polymeric constituents in the low-pressure circuit, and the isoparaffinic solvent is reused for dissolving the free-radical polymerization initiator.

2. The process of claim 1 , wherein the isoparaffinic solvent is separated off in the low-pressure circuit by means of at least one first gas-liquid separator and at least one last gas-liquid separator connected in series, with the temperature being reduced from separator to separator so that the monomeric, oligomeric or polymeric constituents are separated out in a first gas-liquid separator and the isoparaffinic solvent is essentially separated out as liquid in a last gas-liquid separator.

3. The process of claim 1 , wherein the isoparaffinic solvent has a boiling point equal to or less than 150° C.

4. The process of claim 1 , wherein the isoparaffinic solvent has a boiling point equal to or less than 135° C.

5. The process of claim 1 , wherein the isoparaffinic solvent which has been separated off is used without further purification for dissolving the free-radical polymerization initiator.

6. The process of claim 2 , wherein the pressure upstream of the last gas-liquid separator is increased such that the isoparaffinic solvent condenses while ethylene monomer is in a gaseous state.

7. The process of claim 1 , wherein the isoparaffinic solvent has a spontaneous ignition temperature of at least 250° C.

8. The process of claim 1 , wherein the isoparaffinic solvent has a spontaneous ignition temperature of at least 300° C.

9. The process of claim 1 , wherein the isoparaffinic solvent is a mixture of which at least one isoparaffin has a boiling point from 100 to 150° C.

10. The process of claim 1 , wherein the isoparaffinic solvent is a mixture of which at least one isoparaffin has a boiling point from 110 to 140° C.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0705 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0856 →
SECURITY AGREEMENT Recorded Aug 4, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; BASELL POLYOLEFIN GMBH; LYONDELL CHEMICAL COMPANY; EQUISTAR CHEMICALS, L.P.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 021354/0708 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AND PATENT APPLICATIONS Recorded Mar 26, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; EQUISTAR CHEMICALS. LP.; LYONDELL CHEMICAL COMPANY; LYONDELL CHEMICAL TECHNOLOGY, L.P.; LYONDELL PETROCHEMICAL COMPANY; NATIONAL DISTILLERS AND CHEMICAL CORPORATION; OCCIDENTAL CHEMICAL CORPORATION; OLIN CORPORATION; QUANTUM CHEMICAL CORPORATION; BASELL POLYOLEFIN GMBH
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 020704/0562 →
Priority Claims (1)
DE 103 51 262 · Oct 31, 2003 · national
Continuity (2)
Provisional Application 6052526800 · Nov 25, 2003
Related Publication 20070123678A1 · May 31, 2007