IP Library Granted Patent US 7,923,416
Granted Patent B2
US 7,923,416 · App. 12/265,859 · Granted Apr 12, 2011

Method of reducing the viscosity of hydrocarbon fluids

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Quick Facts
Patent No.
US 7,923,416
App. No.
12/265,859
Granted
Apr 12, 2011
Kind
B2
Abstract

This invention relates to methods for reducing the viscosity of hydrocarbon liquids encountered in petroleum operations. The method includes forming a low viscosity emulsion by contacting hydrocarbon liquids with an effective amount of a water-soluble polymer having pendant methyl ether groups.

Claims (16)

1. A method for reducing the viscosity of a hydrocarbon fluid encountered in petroleum operations, the method comprising: contacting said hydrocarbon fluid with an effective amount of a water-soluble polymer to form an emulsion, said polymer having pendant methyl ether groups.

2. The method of claim 1 , wherein the water-soluble polymer is derived by substituting methyl ether groups onto a preformed reactive polymer, said preformed reactive polymer being a vinyl alcohol polymer and said water-soluble polymer having from about 20% to about 100% of available reactive groups of the preformed reactive polymer substituted with methyl ether groups.

3. The method of claim 2 , wherein the preformed reactive polymer is selected from the group consisting of: polyvinyl alcohol, polyvinyl acetate, cellulose, starch, galactomannan, galactoglucomannan, xylan, arabinogalactan, chitan, and combinations thereof.

4. The method of claim 1 , wherein the water-soluble polymer is derived by substituting methyl ether groups onto a preformed reactive polymer, and the water-soluble polymer having from about 20% to about 100% of available reactive groups of the preformed reactive polymer substituted with methyl ether groups.

5. The method of claim 1 , wherein the water-soluble polymer further has up to about 80 mol percent of the available reactive groups substituted with hydrophilic groups other than polyvinyl alcohol.

6. The method of claim 1 , wherein the water-soluble polymer has up to about 50 mol percent of the available reactive groups substituted with hydrophobic groups.

7. The method of claim 6 , wherein the hydrophobic groups have from 2 to about 25 carbons.

8. The method of claim 6 , wherein the hydrophobic groups are selected from the group consisting of: vinyl acetate; propylene oxide; methacrylate; methyl ethacrylate; octadecylacrylate; n-octadecylacrylamide; styrene; methyl styrene; allyl stearate; vinyl stearate; ethene; propene; n-butene; isobutene; pentene; dodecene; octadecene; vinyl ethers higher than methyl; and combinations thereof.

9. The method of claim 1 , wherein the water-soluble polymer is a cellulose ether.

10. The method of claim 9 , wherein the cellulose ether is selected from the group consisting of: methylcellulose; methyl hydroxyethyl cellulose; methyl hydroxypropyl cellulose; carboxymethyl methylcellulose; methyl hydroxybutyl methylcellulose; and combinations thereof.

11. The method of claim 9 , wherein the cellulose ether is a methylcellulose having a degree of substitution from 1.5 to 2.4.

12. The method of claim 9 , wherein the cellulose ether has a molecular weight from about 5,000 to about 150,000.

13. The method of claim 9 , wherein the cellulose ether has pendant groups selected from the group consisting of: hydroxyethyl; hydroxypropyl; carboxymethyl; hydroxybutyl; hydroxyl; and combinations thereof.

14. The method of claim 1 , wherein the effective amount of the water-soluble polymer is from about 100 ppm to about 7%, as polymer actives based upon total volume of the emulsion.

15. The method of claim 1 , wherein the effective amount of the water-soluble polymer is from about 300 ppm to about 4%, as polymer actives based upon total volume of the emulsion.

16. The method of claim 1 , wherein the effective amount of the water-soluble polymer is from about 500 ppm to about 2%, as polymer actives based upon total volume of the emulsion.

Assignments (12)
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jul 17, 2025
From: JPMORGAN CHASE BANK, N.A.
To: CHAMPIONX LLC; APERGY ESP SYSTEMS, LLC; APERGY BMCS ACQUISITION CORP; HARBISON-FISCHER, INC.; NORRIS RODS, INC.,; NORRIS RODS, INC.,; NORRISEAL-WELLMARK, INC.; PCS FERGUSON, INC.; QUARTZDYNE, INC.; US SYNTHETIC CORPORATION
Reel/Frame 072004/0019 →
RELEASE OF SECURITY INTEREST Recorded Jun 7, 2022
From: BANK OF AMERICA, N.A.
To: CHAMPIONX USA INC.
Reel/Frame 060304/0267 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2022
From: ECOLAB USA INC.
To: CHAMPIONX USA INC.
Reel/Frame 059718/0646 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 053250/0001 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 052848/0368 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2017
From: NALCO COMPANY
To: ECOLAB USA INC.
Reel/Frame 042147/0420 →
CHANGE OF NAME Recorded Feb 28, 2017
From: NALCO COMPANY
To: NALCO COMPANY LLC
Reel/Frame 041835/0903 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2017
From: NALCO COMPANY LLC; CALGON CORPORATION; CALGON LLC; ONDEO NALCO ENERGY SERVICES, L.P.
To: ECOLAB USA INC.
Reel/Frame 041836/0437 →
RELEASE OF SECURITY INTEREST Recorded Feb 24, 2017
From: BANK OF AMERICA, N.A.
To: NALCO COMPANY
Reel/Frame 041808/0713 →
RELEASE OF SECURITY INTEREST Recorded Jun 18, 2015
From: BANK OF AMERICA, N.A.
To: NALCO COMPANY
Reel/Frame 035976/0609 →
SECURITY AGREEMENT Recorded May 18, 2009
From: NALCO COMPANY; CALGON LLC; NALCO ONE SOURCE LLC; NALCO CROSSBOW WATER LLC
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 022703/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2008
From: NGUYEN, DUY T.
To: NALCO COMPANY
Reel/Frame 021793/0969 →