IP Library Granted Patent US 9,102,791
Granted Patent B2
US 9,102,791 · App. 13/753,011 · Granted Aug 11, 2015

Alkoxylated sorbitan esters as crude oil emulsion breakers

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Quick Facts
Patent No.
US 9,102,791
App. No.
13/753,011
Granted
Aug 11, 2015
Kind
B2
Abstract

Disclosed herein are alkoxylated sorbitan ester compounds and compositions useful in emulsion breaking applications relating to the production, transportation, storage, and separation of crude oil and natural gas. Also disclosed herein are methods of using the compounds and compositions as emulsion breakers, particularly in applications relating to the production, transportation, storage, and separation of crude oil and natural gas.

Claims (18)

1. An alkoxylated sorbitan ester of formula (I),

wherein,

R 1 is selected from the group consisting of alkyl, alkenyl, and alkynyl;

R 2 , R 3 , and R 4 are each independently selected from the group consisting of hydrogen, alkyl, alkenyl, and alkynyl;

x 1 +x 2 +x 3 =x=0.2 to less than 1 or greater than 50 to 75; and

y 1 +y 2 +y 3 =y=0 or greater than 50 to 250.

2. The compound of claim 1 , wherein R 1 is unsubstituted alkyl.

3. The compound of claim 1 , wherein R 1 is unsubstituted alkyl selected from the group consisting of —CH 2 CH 3 ; —(CH 2 ) 2 CH 3 ; —(CH 2 ) 3 CH 3 ; —(CH 2 ) 4 CH 3 ; —(CH 2 ) 5 CH 3 ; —(CH 2 ) 6 CH 3 ; —(CH 2 ) 7 CH 3 ; —(CH 2 ) 8 CH 3 ; —(CH 2 ) 9 CH 3 ; —(CH 2 ) 10 CH 3 ; —(CH 2 ) 11 CH 3 ; —(CH 2 ) 12 CH 3 ; —(CH 2 ) 13 CH 3 ; —(CH 2 ) 14 CH 3 ; —(CH 2 ) 15 CH 3 ; —(CH 2 ) 16 CH 3 ; —(CH 2 ) 17 CH 3 ; —(CH 2 ) 18 CH 3 ; —(CH 2 ) 19 CH 3 ; —(CH 2 ) 20 CH 3 ; —(CH 2 ) 21 CH 3 ; —(CH 2 ) 22 CH 3 ; —(CH 2 ) 23 CH 3 ; —(CH 2 ) 24 CH 3 ; —(CH 2 ) 25 CH 3 ; —(CH 2 ) 26 CH 3 ; —(CH 2 ) 27 CH 3 ; —(CH 2 ) 28 CH 3 ; —(CH 2 ) 29 CH 3 ; —(CH 2 ) 30 CH 3 ; —(CH 2 ) 31 CH 3 ; —(CH 2 ) 32 CH 3 ; —(CH 2 ) 33 CH 3 ; and —(CH 2 ) 34 CH 3 .

4. The compound of claim 1 , wherein R 1 is —(CH 2 ) 10 CH 3 .

5. The compound of claim 4 , wherein R 2 , R 3 , and R 4 are each independently hydrogen.

6. The compound of claim 1 , wherein R 1 is unsubstituted alkenyl.

7. The compound of claim 1 , wherein R 1 is unsubstituted alkenyl selected from the group consisting of —(CH 2 ) 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 3 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 7 CH 3 ; —(CH 2 ) 3 CH═CHCH 2 CH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 3 CH═CH(CH 2 ) 4 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 3 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 3 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 3 CH═CHCH═CHCH═CHCH═CHCH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 4 CH═CH(CH 2 ) 8 CH 3 ; —(CH 2 ) 4 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 4 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 4 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 4 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 4 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 5 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 5 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 5 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 6 CH═CHCH═CHCH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 6 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 7 CH═CH(CH 2 ) 3 CH 3 ; —(CH 2 ) 7 CH═CH(CH 2 ) 5 CH 3 ; —(CH 2 ) 7 CH═CH(CH 2 ) 7 CH 3 ; —(CH 2 ) 7 CH═CHCH═CHCH═CH(CH 2 ) 3 CH 3 ; —(CH 2 ) 7 CH═CHCH═CH(CH 2 ) 5 CH 3 ; —(CH 2 ) 7 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 7 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 7 CH═CHCH═CHCH 2 CH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 7 CH═CHCH═CHCH═CHCH═CHCH 2 CH 3 ; —(CH 2 ) 7 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 7 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 7 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 9 CH═CH(CH 2 ) 5 CH 3 ; —(CH 2 ) 9 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; —(CH 2 ) 9 CH═CHCH 2 CH═CHCH 2 CH═CHCH 2 CH 3 ; —(CH 2 ) 9 CH═CH(CH 2 ) 7 CH 3 ; —(CH 2 ) 11 CH═CH(CH 2 ) 5 CH 3 ; —(CH 2 ) 11 CH═CH(CH 2 ) 7 CH 3 ; —(CH 2 ) 11 CH═CHCH 2 CH═CH(CH 2 ) 4 CH 3 ; and —(CH 2 ) 13 CH═CH(CH 2 ) 7 CH 3 .

8. The compound of claim 1 , wherein R 1 is —(CH 2 ) 7 CH═CH(CH 2 ) 7 CH 3 .

9. The compound of claim 8 , wherein R 2 , R 3 , and R 4 are each independently hydrogen.

10. A process for preparing a compound of claim 1 wherein R 2 , R 3 , and R 4 are each independently hydrogen, the process comprising:

treating a sorbitan ester of formula (1) with x equivalents of propylene oxide of formula (2) to provide a propoxylated sorbitan ester of formula (3),

and

treating the compound of formula (3) with y equivalents of ethylene oxide of formula (4) to provide a compound of formula (I),

Assignments (7)
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 Dec 7, 2023
From: CHAMPIONX USA INC.
To: CHAMPIONX LLC
Reel/Frame 065799/0403 →
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 Jan 27, 2021
From: ECOLAB USA INC.
To: CHAMPIONX USA INC.
Reel/Frame 055140/0243 →
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 Jan 30, 2013
From: MEYER, G. RICHARD
To: ECOLAB USA INC.
Reel/Frame 029718/0482 →