IP Library Granted Patent US 7,504,438
Granted Patent B1
US 7,504,438 · App. 10/034,661 · Granted Mar 17, 2009

Demulsifiers, their preparation and use in oil bearing formations

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Quick Facts
Patent No.
US 7,504,438
App. No.
10/034,661
Granted
Mar 17, 2009
Kind
B1
Abstract

The invention comprises a polymeric demulsifier, methods of producing the demulsifier and methods of using the demulsifier. The demulsifier is the reaction product of at least one amine-containing group, and optionally a second amine-containing group which includes a tertiary amine group, with a diepoxy- or diglycidyl compound and an additional amine compound subsequently reacted with unreacted epoxy groups. This polymeric composition is subsequently reacted with N-alkylating agent containing compounds to produce novel demulsifiers useful to demulsify oil bearing formations.

Claims (51)

1. A demulsifier composition comprising oligo- and polymeric compounds, wherein the oligo- and polymeric compounds are prepared by

1) reaction of a) an amine having only two reactive amino hydrogens, b) an aliphatic or cycloaliphatic epoxidized olefin having two epoxide groups, and c) a second amine monomer having only two reactive amino hydrogens and a tertiary amine group;

2) optional subsequent reaction of epoxy groups of the oligo- and polymeric reaction products with d) an amine capping monomer having one or two reactive amino hydrogens; and

3) subsequent reaction of amine groups of the oligo- and polymeric reaction products with an N-alkylating agent selected from epichlorohydrin or epibromohydrin reacted polyalkoxide compounds which comprise an oxyalkylene group selected from polyethoxy groups and polypropoxy groups in a propoxy to ethoxy ratio of from about 9 to 1 to about 1 to 9 and methoxy-capped polyethylene oxide.

2. A demulsifier composition comprising the oligo- and polymeric reaction products of at least one first amine having only two reactive hydrogens, selected from the group consisting of methylamine, ethylamine, propylamine, butylamine, sec-butylamine, isobutylamine, 3,3-dimethylbutylamine, hexylamine and benzylamine, 2-amino-1-butanol, 4-amino-1-butanol, 2-amino-2-methyl-1-propanol, 6-amino-1-hexanol, ethanolamine, propanolamine, tris(hydroxymethyl) aminomethane, D-glucamine, 3-amino-1,2-propanediol, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-ethyl-1,3-propanediol, 3-(diemthylamino)propylamine, N,N-dimethylethylenediamine, N,N-diethylethylenediamine, 1-(2-aminoethyl)piperidine, 4-(2-aminoethyl)morpholine, 2-(2-aminoethyl)-1-methylpyrrolidine, 1-(2-aminoethyl)pyrrolidine, 2-(2-aminoethyl)pyridine, 2-(2-aminoethylamino)ethanol, piperazine, 2-methyl piperazine, 2,6-dimethylpiperazine, 2-(methylamido)piperazine, N,N′-bis(2-hydroxyethyl)ethylenediamine, N,N′-dimethylethylenediamine, N,N-dimethyl-1,4-phenylenediamine and N,N′-dimethyl-1,6-hexanediamine;

(b) at least one second amine having only two reactive amino hydrogens and a tertiary amine group selected from the group consisting of 3-(dimethylamino)propylamine, N,N-dimethylethylenediamine, N,N-diethylethylenediamine, 1-(2-aminoethyl)piperidine, 4-(2-aminoethyl)morpholine, 2-(2-aminoethyl)-1-methylpyrrolidine, 1-(2-aminoethyl)pyrrolidine, and 2-(2-aminoethyl)pyridine;

(c) at least one diepoxy-containing compound said diepoxy compound selected from the group consisting of: bis(2,3-epoxypropyl)ether, diglycidyl ether of 1,4-butanediol, diglycidyl other of neopentyl glycol, diglycidyl ether of ethylene glycol, glycerol diglycidyl ether, diglycidyl ether of polyethyleneglycol, diglycidyl ether of polypropylene glycol, the diglycidyl ether from the reaction product of ethylene oxide with propylene oxide, diglycidyl ester of cyclohexane dimethanol and diglycidyl ester of a dimer acid, 1,2,3,4-diepoxybutane; 1,2,7,8-diepoxyoctane, 1,2,9,10-diepoxydecane and 1,2,5,6-diepoxycyclooctane;

(d) at least one amine capping monomer having one or two reactive amine hydrogens, wherein said capping monomer is reacted with terminal epoxy groups on said oligo- and polymeric reaction products, the amine capping monomer being selected from the group consisting of diethanolamine, diisopropanolamine, N-methyl-D-glucamine, N-methylpropylamine, dimethylamine, diethylamine, dipropylamine, diisopropylamine, N,N,N′-trimethyl-1,3-propanediamine, N,N,N′-trimethylethylenediamine, N,N-dimethyl-N′-ethylethylenediamine, N,N,N′-triethylethylenediamine; and

(e) at least one N-alkylating epichlorohydrin capped polyalkylene glycol methyl ether having the following formula:

R8-O—[CH 2 —CH(R9)—O] n —CH 2 —CH(OH)—CH 2 —X where:

R8 is hydrogen, C 1 to C 6 alkyl, C 6 -C 10 aryl, 2-hydroxy-3-chloropropyl, or 2,3-oxopropyl,

R9 is hydrogen, or C 1 to C 6 alkyl,

X is a halogen atom, and n in the range of 1 to 120.

3. The demulsifier composition according to claim 2 , further comprising the oligo- and polymeric reaction product of an amine having only two reactive amino hydrogens selected from the group consisting of; 2-(2-aminoethoxy) ethanol; CH 3 OCH 2 CH 2 O[CH(—CH 3 )CH 2 O] n CH 2 CH(—NH 2 )CH 3 where n is at least one; CH 3 —O—(CH 2 CHR—O) n —CH 2 CH(—CH 3 )NH 2 where R is H or CH 3 and n is at least one; and H 2 N—CH 2 CH 2 OCH 2 CH 2 —OH, a diepoxy-containing compound, and a triepoxy-containing compound.

4. A demulsifier composition comprising oligo- and polymeric reaction products of

(a) a first amine having only two reactive amino hydrogens selected from the group consisting of: ethanolamine, propanolamine, and polyoxyalkylamines according to the formula

R4-(CH 2 CH(R5)O) n —CH 2 CH(CH 3 )NH 2 ,

where R4 is —OCH 3 , R5 is hydrogen or —CH 3 , and n is 1 to 45, 2-(2-aminoethylamino)ethanol, piperazine, N,N-bis(2-hydroxyethyl)ethylenediamine, and N,N′-dimethylethylenediamine and mixtures thereof;

(b) a diepoxy compound selected from the group consisting of diglycidyl ether of 1,4-butanediol, diglycidyl ether of neopentyl glycol, diglycidyl ether of ethylene glycol, diglycidyl ether of polyethyleneglycols, 1,2,3,4-diepoxybutane, 1,2,7,8-diepoxyoctane and mixtures thereof;

(c) an amine capping monomer having one or two reactive amino hydrogens subsequently reacted with terminal epoxy groups, selected from the group consisting of diethanolamine, N-methyl-D-glucamine, N-methylpropylamine, N,N,N′-trimethyl-1,3-propanediamine, N,N,N′-trimethylethylenediamine, and mixtures thereof, and;

(d) an N-alkylating epichlorohydrin capped polyalkylene glycol methyl ether-containing group having the formula:

CH 3 —O—[CH 2 —CH(R9)—O] n —CH 2 —CH(OH)—CH 2 —Cl

where n is 100 to 113 and is R9 is selected from the group consisting of hydrogen and a C 1 to C 6 alkyl group.

5. The demulsifier composition according to claim 4 , wherein (a) further comprises a second amine monomer having only two reactive amino hydrogens and a tertiary amine group selected from the group consisting of 3-(dimethylamino)propylamine, N,N-dimethylethylenediamine, and mixtures thereof.

6. The demulsifier composition according to claim 4 , further comprising at least one C 1 to C 16 alcohol and at least one acid-containing compound.

7. The demulsifier composition according to claim 6 further comprising a compound selected from the group consisting of alkyleneoxide copolymers, oxyalkylated alcohols, organo-phosphate esters, inorganic phosphate esters, polyglycols, resole resins, novalac resins and mixtures thereof.

8. The demulsifier composition according to claim 6 further comprising, an acid selected from the group consisting of arylalkylsulfonic acid; aqueous hydrochloric acid, hydrofluoric, sulfamic, acetic acid, formic acid, nitric acid, citric acid, ethylenediaminetetraacetic acid, nitriloacetic acid and mixtures thereof.

9. A method of treating an oil bearing formation comprising the steps of: charging an oil bearing formation with a demulsifying amount of the demulsifier composition according to claim 6 blended per 1000 gallons of an aqueous organic or aqueous inorganic acid solution.

10. The method of treating an oil bearing formation according to claim 9 wherein the effective amount of demulsifier composition is in the range of 0.01 to about 5 gallons per 1000 gallons of an added aqueous acidic solution.

11. A method of preparing a polymeric demulsifier compound comprising the steps of:

a) reacting 0.5 to 1.4 moles of amines having only two reactive amino hydrogens with 1.0 mole of a diglycidyl ether of a glycol or epoxidized olefin and heating the reactants to between 25° C. to 240° C. for a period of time sufficient for the reaction product to attain a viscosity of at least 80,000 cps; and subsequently

b) capping unreacted glycidyl or epoxy groups on the polymeric reaction product with an amine monomer having only two reactive amino hydrogens and a tertiary amine group; and

c) alkylating amine groups on the polymeric reaction product with a N-alkylating agent-containing group to provide a polymeric demulsifier compound.

12. The method of claim 11 further comprising the step of adding a second amine monomer having only two reactive amino hydrogens and a tertiary amine group to the reaction.

13. The method of claim 11 , further characterized by reacting 0.7 to 1.2 moles of at least one amine having only two active amino hydrogens, and a second amine monomer having only two reactive amine hydrogens and a tertiary amine group with one mole of diglycidyl ether of a glycol or epoxidized olefin between 25° C. to 240° C. for a time period sufficient for the reaction product to reach a viscosity of at least 80,000 cps.

14. The method of claim 11 further characterized by grafting an N-alkylating agent onto the polymer by reacting the polymer and N-alkylating agent a weight ratio of between 1:1 to 8:1 at a pH between 7.5 and 9.0 at a temperature between 60° C. and 95° C. for a time period sufficient to reach a solution viscosity between 200 and 9000 cps.

15. The method of claim 11 further characterized by grafting the N-alkylating agent onto the polymer at a weight ratio of between 1:1 to 8:1 of polymer to N-alkylating agent, at a pH between 7.5 and 9.0 and at a temperature between 85° C. and 95° C. for a time sufficient to produce a viscosity between 200 and 5000 cps.

16. The method of claim 11 wherein the N-alkylating agent is epichlorohydrin capped polyalkylene glycol methyl ether.

17. The method of claim 11 further comprising the step of protonating the polymeric reaction product after steps a) and b) with an acid.

18. A demulsifier composition comprising the polymeric reaction product of

1) 0.8:1 to about 1.3:1 molar equivalents relative to diepoxy-containing compound of at least one first amine-containing group having only two reactive amino hydrogens selected from the group consisting of

(a) methylamine, ethylamine, propylamine, butylamine, sec-butylamine, isobutylamine, 3,3-dimethylbutylamine, hexylamine, benzylamine, 2-amino-1-butanol, 4-amino-1-butanol, 2-amino-2-methyl-1-propanol, 6-amino-1-hexanol, ethanolamine, propanolamine, tris(hydroxymethyl)aminomethane, 1-amino-1-deoxy-D-sorbitol (D-glucamine), 3-amino-1,2-propanediol, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-ethyl-1,3-propanediol, 3-(dimethylamino)propylamine, N,N-dimethylethylenediamine, N,N-diethylethylenediamine, 1-(2-aminoethyl)piperidine, 4-(2-aminoethyl)morpholine, 2-(2-aminoethyl)-1-methylpyrrolidine, 1-(2-aminoethyl)pyrrolidine, 2-(2-aminoethyl)pyridine, 2-(2-aminoethylamino)ethanol, piperazine, 2-methyl piperazine, 2,6-dimethylpiperazine and 2-(methylamido)piperazine, N,N′-bis(2-hydroxyethyl)ethylenediamine, N,N′-dimethylethylenediamine, N,N′-dimethyl-1,4-phenylenediamine and N,N′dimethyl-1,6-hexanediamine;

(b) amines of formula NH 2 -R1-Z 1 ; and

(c) amines of formula HN (R1Z1)—R3—NH—(R1Z1);

wherein R1 is (—CH 2 —CH 2 —O—) n , —(CH 2 —CH(—CH 3 )—O—) n , or —(CH 2 —CH 2 —O—) m —(CH 2 CH(—CH 3 )—O—) n — where n, m and p are 1 to 45; R3 is a C 2 -C 20 alkylene or C 2 -C 20 substituted alkylene wherein the substituent are selected from the group consisting of alkylamido, hydroxy, alkoxy, halo, cyano, aryloxy, alkylcarbonyl, arylcarbonyl, and mixtures thereof; and Z1 is hydrogen, alkyl or acyl;

2) at least one diepoxy-containing compound selected from compounds of formula:

Epoxy-CH 2 —O—(R6—O—) n —Epoxy; and Epoxy-CH 2 —R7—CH 2 -Epoxy

wherein R6 is selected from C 2 to C 20 alkylene; alkyl substituted C 2 to C 20 alkylene, C 2 to C 40 alkoxy, and C 2 to C 40 hydroxy substituted alkoxy; n is 0 to 20; and R7 is a C 2 to C 20 alkylene, or a substituted alkylene; and

3) subsequently reacting the polymeric reaction product of 1) and 2) with at least one N-alkylating agent selected from the group consisting of epihalohydrin capped polyalkylene glycol methyl ether of formula

R8-O—[CH 2 —CH(R9)—O—] n —CH 2 —CH(OH)—CH 2 —X

wherein R8 is selected from hydrogen, C 1 -C 6 alkyl, C 6 -C 10 aryl, 2-hydroxy-3-chloropropyl and 2,3-oxopropyl; R9 is selected from hydrogen and C 1 to C 6 alkyl; n is 1 to 120; and X is a halogen atom.

Assignments (15)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 20, 2022
From: ECOLAB USA INC.
To: CHAMPIONX USA INC.
Reel/Frame 060988/0630 →
RELEASE OF SECURITY INTEREST Recorded Jun 7, 2022
From: BANK OF AMERICA, N.A.
To: CHAMPIONX USA INC.
Reel/Frame 060304/0267 →
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 →
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 →
CHANGE OF NAME Recorded Feb 28, 2017
From: NALCO COMPANY
To: NALCO COMPANY LLC
Reel/Frame 041836/0364 →
RELEASE OF SECURITY INTEREST Recorded Feb 28, 2017
From: CITICORP NORTH AMERICA, INC.
To: NALCO COMPANY
Reel/Frame 041837/0366 →
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 →
MERGER Recorded Dec 2, 2008
From: NALCO ENERGY SERVICES L.P
To: NALCO COMPANY
Reel/Frame 021914/0031 →
CHANGE OF NAME Recorded Mar 14, 2006
From: ONDEO NALCO ENERGY SERVICES, L.P.
To: NALCO ENERGY SERVICES, L.P.
Reel/Frame 017304/0646 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2002
From: TREYBIG, DUANE S.; CHANG, K.T.; WILLIAMS, DENNIS A.
To: ONDEO NALCO ENERGY SERVICES, L.P.
Reel/Frame 012660/0309 →