IP Library Granted Patent US 8,318,647
Granted Patent B2
US 8,318,647 · App. 12/691,300 · Granted Nov 27, 2012

Production of polyol ester lubricants for refrigeration systems

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 8,318,647
App. No.
12/691,300
Granted
Nov 27, 2012
Kind
B2
Abstract

A poly(neopentylpolyol) ester composition is produced by reacting a neopentylpolyol having the formula: wherein each R is independently selected from the group consisting of CH 3 , C 2 H 5 and CH 2 OH and n is a number from 1 to 4, with at least one monocarboxylic acid having 2 to 15 carbon atoms in the presence of an acid catalyst and at an initial mole ratio of carboxyl groups to hydroxyl groups of greater than 0.5:1 to 0.95:1 to form a partially esterified poly(neopentylpolyol) composition. Then the partially esterified poly(neopentylpolyol) composition is reacted with additional monocarboxylic acid having 2 to 15 carbon atoms to form a final poly(neopentylpolyol) ester composition.

Claims (45)

1. A poly(neopentylpolyol) ester composition produced by:

(i) reacting pentaerythritol with a mixture of monocarboxylic acids selected from n-pentanoic acid, iso-pentanoic acid, n-hexanoic acid, n-heptanoic acid, n-octanoic acid, n-nonanoic acid and iso-nonanoic acid,

wherein said mixture comprises from about 2 to about 6 moles of n-pentanoic acid and from about 0 to about 3.5 moles of n-heptanoic acid per mole of iso-nonanoic acid, in the presence of an acid catalyst and at an initial mole ratio of carboxyl groups to hydroxyl groups of greater than 0.5:1 to 0.95:1 to form a partially esterified poly(neopentylpolyol) composition;

and

(ii) reacting the partially esterified poly(neopentylpolyol) composition produced in (i) with additional monocarboxylic acid, wherein the additional monocarboxylic acid employed comprises the same carboxylic acids employed in (i)

and

wherein the polyol ester composition comprises monopentaerythritol esters, dipentaerythritol esters and polypentaerythritol esters in a weight ratio of mono- to di- to polypentaerythritol esters of about 76:16:8 to about 60:20:20 and has a viscosity index in excess of 95.

2. The ester composition of claim 1 , wherein the initial mole ratio of carboxyl groups to hydroxyl groups is from 0.7:1 to 0.85:1.

3. The ester composition of claim 1 , wherein said mixture of monocarboxylic acids comprises from about 1.75 to about 2.25 moles of n-pentanoic acid and 0.75 to about 1.25 moles of n-heptanoic acid per mole of iso-nonanoic acid.

4. The ester composition of claim 2 , wherein said mixture of monocarboxylic acids comprises from about 1.75 to about 2.25 moles of n-pentanoic acid and 0.75 to about 1.25 moles of n-heptanoic acid per mole of iso-nonanoic acid.

5. A poly(neopentylpolyol) ester composition produced by:

(i) reacting pentaerythritol with a mixture of monocarboxylic acids selected from n-pentanoic acid, iso-pentanoic acid, n-hexanoic acid, n-heptanoic acid, n-octanoic acid, n-nonanoic acid and iso-nonanoic acid,

wherein said mixture comprises from about 1 to about 10 moles of iso-nonanoic acid and 0 to about 1 moles of n-heptanoic acid per mole of iso-pentanoic acid,

in the presence of an acid catalyst and at an initial mole ratio of carboxyl groups to hydroxyl groups of greater than 0.5:1 to 0.95:1 to form a partially esterified poly(neopentylpolyol) composition;

and

(ii) reacting the partially esterified poly(neopentylpolyol) composition produced in (i) with additional monocarboxylic acid, wherein the additional monocarboxylic acid employed comprises the same carboxylic acids employed in (i)

and

wherein the polyol ester composition comprises monopentaerythritol esters, dipentaerythritol esters and polypentaerythritol esters in a weight ratio of mono- to di- to polypentaerythritol esters of about 76:16:8 to about 60:20:20 and has a viscosity index in excess of 95.

6. The ester composition of claim 5 , wherein the initial mole ratio of carboxyl groups to hydroxyl groups is from 0.7:1 to 0.85:1.

7. A working fluid comprising (a) a refrigerant and (b) a poly(neopentylpolyol) ester composition produced by:

(i) reacting pentaerythritol with a mixture of monocarboxylic acids selected from n-pentanoic acid, iso-pentanoic acid, n-hexanoic acid, n-heptanoic acid, n-octanoic acid, n-nonanoic acid and iso-nonanoic acid,

wherein said mixture comprises from about 2 to about 6 moles of n-pentanoic acid and from about 0 to about 3.5 moles of n-heptanoic acid per mole of iso-nonanoic acid,

in the presence of an acid catalyst and at an initial mole ratio of carboxyl groups to hydroxyl groups of greater than 0.5:1 to 0.95:1 to form a partially esterified poly(neopentylpolyol) composition;

and

(ii) reacting the partially esterified poly(neopentylpolyol) composition produced in (i) with additional monocarboxylic acid, wherein the additional monocarboxylic acid employed comprises the same carboxylic acids employed in (i)

and

wherein the polyol ester composition comprises monopentaerythritol esters, dipentaerythritol esters and polypentaerythritol esters in a weight ratio of mono- to di- to polypentaerythritol esters of about 76:16:8 to about 60:20:20 and has a viscosity index in excess of 95.

8. The working fluid of claim 7 , wherein the initial mole ratio of carboxyl groups to hydroxyl groups is from 0.7:1 to 0.85:1.

9. The working fluid of claim 7 , wherein said mixture of monocarboxylic acids comprises from about 1.75 to about 2.25 moles of n-pentanoic acid and 0.75 to about 1.25 moles of n-heptanoic acid per mole of iso-nonanoic acid.

10. The working fluid of claim 8 , wherein said mixture of monocarboxylic acids comprises from about 1.75 to about 2.25 moles of n-pentanoic acid and 0.75 to about 1.25 moles of n-heptanoic acid per mole of iso-nonanoic acid.

11. The working fluid of claim 7 , wherein the refrigerant is a hydrofluorocarbon, a fluorocarbon or a mixture thereof.

12. The working fluid of claim 11 , wherein the refrigerant comprises a hydrofluorocarbon or fluorocarbon compound selected from difluoroethane (R-32) 1,1,1,2-tetrafluoroethane (R-134a), 1,1,2,2-tetrafluoroethane (R-134), pentafluoroethane (R-125) and tetrafluoropropene (R-1234yf).

13. The working fluid of claim 7 , wherein the refrigerant is selected from 1,1,1,2-tetrafluoroethane (R-134a), tetrafluoropropene (R-1234yf) and a mixture of 50 wt % difluoromethane and 50 wt % pentafluoroethane (R-410A).

14. A working fluid comprising (a) a refrigerant and (b) a poly(neopentylpolyol) ester composition produced by:

(i) reacting pentaerythritol with a mixture of monocarboxylic acids selected from n-pentanoic acid, iso-pentanoic acid, n-hexanoic acid, n-heptanoic acid, n-octanoic acid, n-nonanoic acid and iso-nonanoic acid,

wherein said mixture comprises from about 1 to about 10 moles of iso-nonanoic acid and 0 to about 1 moles of n-heptanoic acid per mole of iso-pentanoic acid,

in the presence of an acid catalyst and at an initial mole ratio of carboxyl groups to hydroxyl groups of greater than 0.5:1 to 0.95:1 to form a partially esterified poly(neopentylpolyol) composition;

and

(ii) reacting the partially esterified poly(neopentylpolyol) composition produced in (i) with additional monocarboxylic acid, wherein the additional monocarboxylic acid employed comprises the same carboxylic acids employed in (i)

and

wherein the polyol ester composition comprises monopentaerythritol esters, dipentaerythritol esters and polypentaerythritol esters in a weight ratio of mono- to di- to polypentaerythritol esters of about 76:16:8 to about 60:20:20 and has a viscosity index in excess of 95.

15. The working fluid of claim 14 , wherein the initial mole ratio of carboxyl groups to hydroxyl groups is from 0.7:1 to 0.85:1.

16. The working fluid of claim 14 , wherein the refrigerant is a hydrofluorocarbon, a fluorocarbon or a mixture thereof.

17. The working fluid of claim 16 , wherein the refrigerant comprises a hydrofluorocarbon or fluorocarbon compound selected from difluoroethane (R-32) 1,1,1,2-tetrafluoroethane (R-134a), 1,1,2,2-tetrafluoroethane (R-134), pentafluoroethane (R-125) and tetrafluoropropene (R-1234yf).

18. The working fluid of claim 14 , wherein the refrigerant is selected from 1,1,1,2-tetrafluoroethane (R-134a), tetrafluoropropene (R-1234yf) and a mixture of 50 wt % difluoromethane and 50 wt % pentafluoroethane (R-410A).

Assignments (13)
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 →
CONFIRMATORY LICENSE Recorded Jan 28, 2015
From: CHEMTURA CORPORATION
To: ENERGY, UNITED STATES DEPARTMENT OF
Reel/Frame 034893/0215 →
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 →
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 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2010
From: CARR, DALE; HUTTER, JEFFREY; KELLEY, RICHARD; HESSELL, EDWARD T.; URREGO, ROBERTO
To: CHEMTURA CORPORATION
Reel/Frame 024173/0941 →
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 →