IP Library Granted Patent US 6,964,940
Granted Patent B1
US 6,964,940 · App. 10/338,442 · Granted Nov 15, 2005

Method of preparing quaternized amidoamine surfactants

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Quick Facts
Patent No.
US 6,964,940
App. No.
10/338,442
Granted
Nov 15, 2005
Kind
B1
Abstract

This invention is a method of preparing a quaternized amidoamine surfactant comprising reacting an amidotertiaryamine of formula with methyl halide and alkylene oxide, an aqueous quaternized amidoamine surfactant composition, a gelled aqueous composition comprising the quaternized amidoamine surfactant composition and one or more salts or alcohols and use of the gelled aqueous composition for fracturing subterranean formations.

Claims (38)

1. A method of preparing a quaternized amidoamine surfactant of formula

wherein

R 1 is selected from the group consisting of C 12 –C 30 alkyl, C 12 –C 30 alkenyl, C 12 –C 30 arylalkyl and C 12 –C 30 cycloalkylalkyl,

R 2 and R 3 are independently selected at each occurrence from hydrogen or C 1 –C 4 alkyl,

R 4 and R 5 are independently selected from C 1 –C 4 alkyl, C 1 –C 4 alkoxyalkyl and C 1 –C 4 hydroxyalkyl,

X is halide; and

n is an integer from 1 to about 10

comprising reacting an amidotertiaryamine of formula

with methyl halide and alkylene oxide.

2. The method of claim 1 wherein the methyl halide is added prior to the alkylene oxide.

3. The method of claim 2 wherein additional methyl halide is added subsequently to the alkylene oxide.

4. The method of claim 1 wherein the alkylene oxide is ethylene oxide.

5. The method of claim 1 wherein the reaction is carried out in a C 1 –C 4 alcohol.

6. The method of claim 5 wherein the alcohol is isopropanol.

7. The method of claim 1 wherein R 1 is selected from the group consisting of C 12 –C 30 alkyl and C 12 –C 30 alkenyl.

8. The method of claim 1 wherein R 1 is C 12 –C 30 alkenyl.

9. The method of claim 1 wherein R 1 is C 18 –C 30 alkenyl.

10. The method of claim 1 wherein R 1 is C 18 –C 30 alkenyl; R 2 and R 3 are hydrogen; R 4 and R 5 are independently selected from C 1 –C 2 alkyl and C 1 –C 2 hydroxyalkyl; and n is an integer of 2 to about 6.

11. The method of claim 10 wherein R 4 and R 5 are methyl.

12. A quaternized amidoamine surfactant prepared according to the method of claim 1 .

13. A quaternized amidoamine surfactant composition comprising about 40 to about 80 weight percent of the quaternized amidoamine surfactant of claim 12 and about 20 to about 60 weight percent of one or more C 1 –C 4 alcohols.

14. The quaternized amidoamine surfactant composition of claim 13 wherein the C 1 –C 4 alcohol is isopropanol.

15. An aqueous composition comprising

a) about 75 to about 90 weight percent of the quaternized amidoamine surfactant composition of claim 12 ;

b) about 1 to about 15 weight percent of one or more C 2 –C 4 diols; and

c) about 1 to about 10 weight percent water.

16. The aqueous composition of claim 15 wherein the C 2 –C 6 diol is 1,2-propane diol.

17. The aqueous composition of claim 15 that has a pour point of less than 40° F.

18. A gelled aqueous composition comprising

a) about 0.5 to about 10 weight percent of the aqueous composition of 15;

b) about 0.5 to about 10 weight percent of one or more salts or one or more C 4 –C 10 alcohols; and

c) water.

19. The gelled aqueous composition of claim 18 wherein the salts are selected from potassium chloride, ammonium chloride, sodium salicylate and mixtures thereof.

20. The gelled aqueous composition of claim 18 wherein the C 4 –C 10 alcohol is selected from the group consisting of hexanol, octanol and decanol.

21. The gelled aqueous composition of claim 18 further comprising about 0.5 to about 8 pounds per gallon of a particulate proppant suspended therein.

22. A method of treating a well in a subterranean formation comprising pumping into the well the gelled aqueous composition of claim 18 .

23. The method of claim 22 wherein the treating is selected from drilling, hydraulic fracturing, gravel placement, scale removing and mud cake removing operations.

24. A method of fracturing a subterranean formation comprising pumping into the formation at a pressure sufficient to fracture the formation the gelled aqueous composition of claim 21 .

Assignments (18)
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 059484/0005 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 052848/0368 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 053250/0001 →
CHANGE OF NAME Recorded Dec 17, 2019
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051322/0583 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 29, 2019
From: AIR PRODUCTS AND CHEMICALS, INC.
To: EVONIK DEGUSSA GMBH
Reel/Frame 050862/0921 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2017
From: NALCO COMPANY
To: ECOLAB USA INC.
Reel/Frame 042147/0420 →
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 28, 2017
From: CITICORP NORTH AMERICA, INC.
To: NALCO COMPANY
Reel/Frame 041837/0366 →
CHANGE OF NAME Recorded Feb 28, 2017
From: NALCO COMPANY
To: NALCO COMPANY LLC
Reel/Frame 041836/0364 →
RELEASE OF SECURITY INTEREST Recorded Feb 24, 2017
From: BANK OF AMERICA, N.A.
To: NALCO COMPANY
Reel/Frame 041808/0713 →
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 Apr 4, 2008
From: TOMAH PRODUCTS, INC.
To: AIR PRODUCTS AND CHEMICALS, INC.
Reel/Frame 020753/0627 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEMT TO ADD ADDRESS TO RECEIVING PARTIES: TOMAH PRODUCTS, INC., P.O. BOX 388, MILTON, WISCONSIN 53563 PREVIOUSLY RECORDED ON REEL 017176 FRAME 0848. ASSIGNOR(S) HEREBY CONFIRMS THE NALCO ENERGY SERVICES, L.P.. Recorded Mar 2, 2006
From: NALCO ENERGY SERVICES, L.P.; TOMAH PRODUCTS, INC.
To: NALCO COMPANY; TOMAH PRODUCTS, INC.
Reel/Frame 017240/0250 →
MERGER Recorded Feb 17, 2006
From: NALCO ENERGY SERVICES, L.P.
To: NALCO COMPANY
Reel/Frame 017176/0848 →
CHANGE OF NAME Recorded Aug 18, 2005
From: ONDEO NALCO ENERY SERVICES, L.P.; TOMAH PRODUCTS, INC.
To: NALCO ENERGY SERVICES, L.P.; TOMAH PRODUCTS, INC.
Reel/Frame 016896/0503 →
GRANT OF SECURITY INTEREST Recorded Dec 8, 2003
From: ONDEO NALCO ENERGY SERVICES, L.P.
To: CITICORP NORTH AMERICA, INC. AS ADMINISTRATIVE AGENT
Reel/Frame 014797/0293 →