Emulsifier for synthetic-based mud, process for preparation, and drilling method

Patent metadata

Field	Value
Publication number	US-12454639-B2
Application number	US-202118028283-A
Country	US
Kind code	B2
Filing date	Jan 29, 2021
Priority date	Sep 24, 2020
Publication date	Oct 28, 2025
Grant date	Oct 28, 2025

Abstract

Improved emulsifier for synthetic-based mud, process for preparation, and drilling method. The emulsifier has the formula (II) wherein each R 1 is a C 4 to C 30 alkyl; R 2 , R 3 , R 5 , and R 6 are each independently selected from H, C 1 to C 4 alkyl, C 1 to C 4 alkoxyalkyl, and C 1 to C 4 hydroxyalkyl; n and m are independently integers from 1 to 10; and y is an integer from 1 to 5. It is prepared by reacting a polyalkyleneamine with a monocarboxylic acid to form a first reaction product, reacting the first reaction product with a dicarboxylic acid to form a second reaction product, and heat treating the second reaction product to form an isomer. The drilling fluid contains the emulsifier, an oleaginous phase, and a non-oleaginous phase, and during use is circulated in a wellbore.

First claim

What is claimed:

1. An emulsifier composition, comprising:
an iso-amidoamine prepared by a process comprising the steps of:
(1) reacting a polyalkyleneamine having from 4 to 30 carbon atoms, at least one secondary amine group, and at least two primary amine groups, with a monocarboxylic acid having from 4 to 30 carbon atoms or an acyl halide or hydrocarbyl ester thereof, to form a first reaction product comprising a polyalkyleneamidoamine derivative of the polyalkyleneamine;
(2) reacting the first reaction product from step (1) with a dicarboxylic acid selected from maleic acid, fumaric acid, maleic anhydride, and combinations thereof to form a second reaction product an acid-substituted amidoamine; and
(3) heat treating the maleated amidoamine from step (2) at a temperature and for a time sufficient to form a heat treatment product comprising an isomer of the acid-substituted amidoamine, wherein the heat treatment product has an acid number less than an acid number of the second reaction product;

about 30-80 wt % of the heat treatment product from step (3); and
about 70-20 wt % of one or more other components,
wherein the one or more other components comprise a hydrocarbyl ethoxylate having the formula RO—(CH 2 CH 2 O) n H wherein R is a C 5-22 (C 16-22 ) hydrocarbyl group and n is an integer in the range of 2 to 30.

2. The emulsifier composition of claim 1 , wherein the polyalkyleneamine has the formula:

where R 1 , R 7 , and R 8 are hydrogen; R 2 , R 3 , R 5 , and R 6 are each independently selected from H, C 1 to C 4 alkyl, C 1 to C 4 alkoxyalkyl, and C 1 to C 4 hydroxyalkyl; n and m are an integers from 1 to 10; and y is an integer from 1 to 5;
wherein the monocarboxylic acid is tall oil fatty acid (TOFA), stearic acid, isostearic acid, or a combination thereof, and the dicarboxylic acid is maleic anhydride.

3. The emulsifier composition of claim 1 , wherein the polyalkyleneamidoamine derivative from step (1) has the formula:

where each R 1 is a C 4 to C 30 hydrocarbyl; R 2 , R 3 , R 5 , and R 6 are each independently selected from H, C 1 to C 4 alkyl, C 1 to C 4 alkoxyalkyl, and C 1 to C 4 hydroxyalkyl; R 4 is hydrogen; n and m are independently integers from 1 to 10; and y is an integer from 1 to 5.

4. The emulsifier composition of claim 1 , wherein step (1) comprises contacting the polyalkyleneamine and the monocarboxylic acid at approximately 110-140° C. in a closed reactor, to control removal of water formed from amide condensation, and to control imidazoline formation to less than 30%, based on the total moles of the polyalkyleneamine, the polyalkyleneamidoamine derivative, and the imidazoline in the first reaction product.

5. The emulsifier composition of claim 1 , wherein a reaction mixture in step (1) comprises a molar ratio of the polyalkyleneamine and the monocarboxylic acid from 1:1.2 to 1:2.8.

6. The emulsifier composition of claim 1 , wherein the acid-substituted amidoamine from step (2) is a compound (I) according to the formula:

where each R 1 is a C4 to C30 hydrocarbyl; R 2 , R 3 , R 5 , and R 6 are each independently selected from H, C 1 to C 4 alkyl, C 1 to C 4 alkoxyalkyl, and C 1 to C 4 hydroxyalkyl; m and n are integers from 1 to 10; and y is an integer from 1 to 5.

7. The emulsifier composition of claim 1 , wherein step (2) comprises contacting the first reaction product and the dicarboxylic acid at approximately 70-100° C., for about 0.5-2 h, wherein a molar ratio of the polyalkyleneamidoamine derivative and the dicarboxylic acid is from 1:0.8 to 1:1.2.

8. The emulsifier composition of claim 1 , wherein the heat treatment in step (3) is conducted at a temperature above 140° C. and/or for a period of time greater than 2 hours.

9. The emulsifier composition of claim 1 , wherein the heat treatment product of step (3) is controlled for an acid number less than 35 mg KOH/gram, an amine number less than 10 mg KOH/gram, and a viscosity of less than 800 centipoise at 50° C. when measured at a dilution of 50 wt % in an IO1618 base oil.

10. An invert drilling fluid, comprising:
(a) an oleaginous external phase;
(b) a non-oleaginous internal phase;
(c) the emulsifier composition of claim 1 ;
(d) optionally one or more rheology additives; and
(e) optionally one or more wetting additives.

11. The invert drilling fluid of claim 10 , further comprising a wetting additive comprising a hydrocarbyl ethoxylate having the formula RO—(CH 2 CH 2 O) n H wherein R is a C 5-22 hydrocarbyl group and n is an integer in the range of 2 to 30.

12. A process for preparing an invert wellbore fluid, comprising the steps of:
(A) making an emulsifier composition, comprising the steps of:
(1) reacting a polyalkyleneamine having from 4 to 30 carbon atoms, at least one secondary amine group, and at least two primary amine groups, with a monocarboxylic acid having from 4 to 30 carbon atoms or an acyl halide or hydrocarbyl ester thereof, to form a first reaction product comprising a polyalkyleneamidoamine derivative of the polyalkyleneamine;
(2) reacting the first reaction product from step (1) with a dicarboxylic acid selected from maleic acid, fumaric acid, maleic anhydride, and combinations thereof to form a second reaction product an acid-substituted amidoamine; and
(3) heat treating the maleated amidoamine from step (2) at a temperature and for a time sufficient to form a heat treatment product comprising an isomer of the acid-substituted amidoamine, wherein the heat treatment product has an acid number less than an acid number of the second reaction product,
wherein the heat treatment product from step (3) comprises iso-amidoamine compound (II) or a mixture of iso-amidoamine compound (II) with acid-substituted amidoamine compound (I) and/or formyl-substituted amidoamine compound (III), according to the formulae:

wherein each R 1 is a C 4 to C 30 hydrocarbyl; R 2 , R 3 , R 5 , and R 6 are each independently selected from H, C to C4 alkyl, C 1 to C 4 alkoxyalkyl, and C 1 to C 4 hydroxyalkyl; n and m are independently integers from 1 to 10; and y is an integer from 1 to 5; and
wherein molar proportions of compounds (I), (II), and (III), are optionally 0-90:10-100:0-60 based on the total moles of compounds (I), (II), and (III), present in the emulsifier composition; and

(B) formulating the emulsifier composition in an emulsifying amount in an invert wellbore fluid further comprising an oleaginous external phase, a non-oleaginous internal phase, one or more rheology additives, and one or more wetting additives, wherein the one or more wetting additives comprise a hydrocarbyl ethoxylate having the formula RO—(CH 2 CH 2 O) n H wherein R is a C 5-22 hydrocarbyl group and n is an integer in the range of 2 to 30.

13. The process of claim 12 , wherein the polyalkyleneamine has the formula

where R 1 , R 7 , and R 8 are hydrogen; R 2 , R 3 , R 5 , and R 6 are each independently selected from H, C 1 to C 4 alkyl, C 1 to C 4 alkoxyalkyl, and C 1 to C 4 hydroxyalkyl; n and m are an integers from 1 to 10; and y is an integ

Assignees

• Schlumberger Technology Corp

Inventors

• Khramov Dimitri M
• Barmatov Evgeny Borisovich

Classifications

• C09K23/16

  Amines or polyamines · CPC title

• C09K23/28

  Aminocarboxylic acids (proteins and protein hydrolysates C09K23/30) · CPC title

• C09K23/22

  Amides or hydrazides · CPC title

• C09K8/36 Primary

  Water-in-oil emulsions · CPC title