IP Library Granted Patent US 8,080,699
Granted Patent B2
US 8,080,699 · App. 12/549,559 · Granted Dec 20, 2011

Two-stage process and system for forming high viscosity polyalphaolefins

Assignee: Chemtura Corporation
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,080,699
App. No.
12/549,559
Granted
Dec 20, 2011
Kind
B2
Abstract

A final polymer product is formed using a two-stage process and system. In the first stage, a catalyst system is used to polymerize an alpha-olefin monomer to form an effluent. In the second stage, additional alpha-olefin monomer is supplied and is polymerized in the presence of the effluent from the first stage. The second stage produces the final polymer product, which may have a lower molecular weight and viscosity than the polymer formed in the first stage. The final polymer product may be used as a base stock for lubricant compositions.

Claims (42)

1. A process for forming a final polymer product comprising:

(a) polymerizing a first olefin monomer in a first reaction zone in the presence of a catalyst system comprising a catalyst to form an effluent comprising a first polymer having a first viscosity and activated catalyst; and

(b) polymerizing a second olefin monomer in a second reaction zone in the presence of the first polymer and the catalyst to form the final polymer product having a second viscosity,

wherein the first polymer has a weight average molecular weight of from 500 to 10,000 and the final polymer product has a weight average molecular weight of from 500 to 8,000 and the final polymer product has a kinematic viscosity at 100° C. of from 20-1000 cSt.

2. The process of claim 1 , further comprising the step of:

(c) directing the first effluent or a portion thereof from the first reaction zone to the second reaction zone.

3. The process of claim 1 , wherein the first olefin monomer and the second olefin monomer comprise alpha-olefin monomers having from 2 to 20 carbon atoms.

4. The process of claim 1 , wherein the first olefin monomer and the second olefin monomer comprise 1-decene.

5. The process of claim 1 , wherein the first olefin monomer is the same as the second olefin monomer.

6. The process of claim 1 , further comprising the step of:

(d) loading a seed composition to the first reaction zone to activate the catalyst.

7. The process of claim 6 , further comprising the step of polymerizing at least a portion of the first polymer in the second reaction zone in the presence of the activated catalyst.

8. The process of claim 1 , wherein the second olefin monomer is only polymerized in the presence of the catalyst system in the effluent without the addition of a separate catalyst system.

9. A process for forming a final polymer product comprising:

(a) polymerizing a first olefin monomer in a first reaction zone in the presence of a catalyst system comprising a catalyst to form an effluent comprising a first polymer having a first viscosity and activated catalyst; and

(b) polymerizing a second olefin monomer in a second reaction zone in the presence of the first polymer and the catalyst to form the final polymer product having a second viscosity,

wherein the first polymer has a weight average molecular weight of from 4,000 to 10,000 and the final polymer product has a weight average molecular weight of from 2,500 to 9,000 and the final polymer product has a kinematic viscosity at 100° C. of from 70 to 140 cSt.

10. The process of claim 1 , wherein the final polymer product has a weight average molecular weight that is at least 50% less than the first polymer.

11. The process of claim 1 , wherein first polymer has a kinematic viscosity at 100° C. of from 20 to 500 cSt.

12. The process of claim 1 , wherein final polymer product has a kinematic viscosity at 100° C. of from 20 to 60 cSt.

13. The process of claim 1 , wherein the final polymer product has a kinematic viscosity at 100° C. of from 70 to 140 cSt.

14. The process of claim 1 , wherein the first viscosity is greater than the second viscosity.

15. The process of claim 1 , wherein the first viscosity is substantially equal to the second viscosity.

16. The process of claim 1 , wherein the molar ratio of the first olefin monomer to the second olefin monomer is from 4:1 to 1:4.

17. The process of claim 1 , wherein the first reaction zone is heated to a first temperature of from 25 to 45° C.

18. The process of claim 1 , wherein the second reaction zone is heated to a second temperature of from 30 to 55° C.

19. The process of claim 1 , wherein the residence time in the first reaction zone is from 1 to 15 hrs.

20. The process of claim 1 , wherein the residence time in the second reaction zone is from 0.25 to 7 hrs.

21. The process of claim 1 , wherein the ratio of the residence time in the first reaction zone to the residence time in the second reaction zone is from 1:4 to 4:1.

22. The process of claim 1 , wherein the catalyst system comprises an alkyl-halide and an alkyl-aluminum.

23. The process of claim 1 , wherein the catalyst system comprises isobutyl bromide and triethylaluminum.

24. The process of claim 1 , wherein the process is a continuous process.

25. The process of claim 9 , further comprising the step of:

(c) directing the first effluent or a portion thereof from the first reaction zone to the second reaction zone.

26. The process of claim 9 , wherein the first olefin monomer and the second olefin monomer comprise alpha-olefin monomers having from 2 to 20 carbon atoms.

27. The process of claim 9 , wherein the first olefin monomer and the second olefin monomer comprise 1-decene.

28. The process of claim 9 , wherein the first olefin monomer is the same as the second olefin monomer.

29. The process of claim 9 , further comprising the step of:

(d) loading a seed composition to the first reaction zone to activate the catalyst.

30. The process of claim 9 , further comprising the step of polymerizing at least a portion of the first polymer in the second reaction zone in the presence of the activated catalyst.

31. The process of claim 9 , wherein the second olefin monomer is only polymerized in the presence of the catalyst system in the effluent without the addition of a separate catalyst system.

32. The process of claim 9 , wherein the catalyst system comprises an alkyl-halide and an alkyl-aluminum.

Assignments (12)
MERGER AND CHANGE OF NAME Recorded Sep 7, 2018
From: CHEMTURA CORPORATION; LANXESS SOLUTIONS US INC.
To: LANXESS SOLUTIONS US INC.
Reel/Frame 046811/0599 →
RELEASE OF AMENDED AND RESTATED SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 12, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
Reel/Frame 042452/0759 →
RELEASE OF THIRD LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 12, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
Reel/Frame 042452/0894 →
RELEASE OF FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042447/0508 →
RELEASE OF SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042449/0001 →
THIRD LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jul 18, 2014
From: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 033360/0325 →
AMENDED AND RESTATED SECOND LIEN INTELLECTUAL PROPERY SECURITY AGREEMENT Recorded Jul 18, 2014
From: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 033360/0225 →
FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT. Recorded Mar 21, 2011
From: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 026028/0622 →
INTELLECTUAL PROPERTY SECURITY RELEASE AGREEMENT Recorded Mar 21, 2011
From: CITIBANK, N.A.
To: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; ASCK, INC; BIOLAB COMPANY STORE, LLC; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIOLAB TEXTILES ADDITIVES, LLC; BIOLAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON MONOCHEM, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GT SEED TREATMENT, INC.; ISCI, INC; GREAT LAKES CHEMICAL GLOBAL, INC.; HOMECARE LABS, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; NAUGATUCK TREATMENT COMPANY; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); MONOCHEM, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC; WRL OF INDIANA, INC.; BIOLAB FRANCHISE COMPANY, LLC
Reel/Frame 026039/0142 →
SECDOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Mar 21, 2011
From: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORORATED; CROMPTON HOLDING CORPORATION; CLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; HAOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
To: BANK OF AMERICA, N. A.
Reel/Frame 027881/0347 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 22, 2010
From: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; AQUA CLEAR INDUSTRIES, LLC; ASCK, INC.; ASEPSIS, INC.; BIOLAB COMPANY STORE, LLC; BIOLAB FRANCHISE COMPANY, LLC; BIOLAB TEXTILE ADDITIVES, LLC; BIO-LAB, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; CROMPTON MONOCHEM, INC.; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; ISCI, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; MONOCHEM, INC.; NAUGATUCK TREATMENT COMPANY; RECREATIONAL WATER PRODUCTS, INC.; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); WEBER CITY ROAD LLC; WRL OF INDIANA, INC.
To: CITIBANK, N.A.
Reel/Frame 023998/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2009
From: KNOWLES, DANIEL C.; FABIAN, JESUS R.
To: CHEMTURA CORPORATION
Reel/Frame 023393/0776 →
Continuity (1)
Related Publication 20110054126A1 · Mar 3, 2011