U.S. patent application number 13/097314 was filed with the patent office on 2011-08-25 for deep eutectic solvents and applications.
This patent application is currently assigned to Shrieve Chemical Products, Inc.. Invention is credited to Richard F. MILLER.
Application Number | 20110207633 13/097314 |
Document ID | / |
Family ID | 41114704 |
Filed Date | 2011-08-25 |
United States Patent
Application |
20110207633 |
Kind Code |
A1 |
MILLER; Richard F. |
August 25, 2011 |
DEEP EUTECTIC SOLVENTS AND APPLICATIONS
Abstract
A method of solubilizing/removing cellulose or
chemically-modified cellulosic polymers utilized in subterranean
drilling operations such as fracturing. The method involves
introducing a deep eutectic solvent (DES) into a subterranean
region. Deep eutectic solvents useful as cellulose solvents include
quaternary ammonium compounds, including choline chloride and
chlorcholine chloride, reacted with a compound selected from
amides, amines, carboxylic acids alcohols, and metal halides. The
DES material can be pumped downhole after fracturing operations to
remove cellulosic material used, for example, to thicken fracturing
fluid which is left behind in the created fractures, on the face of
the formation, along the wellbore, or elsewhere within the
subterranean region. The DES can be used alone or in a sequential
treatment protocol, whereby the DES is introduced into the
subterranean region, followed by post-treatment introduction of
water, caustic, acid or anhydride into the subterranean as a
flush.
Inventors: |
MILLER; Richard F.; (Humble,
TX) |
Assignee: |
Shrieve Chemical Products,
Inc.
The Woodlands
TX
|
Family ID: |
41114704 |
Appl. No.: |
13/097314 |
Filed: |
April 29, 2011 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12410662 |
Mar 25, 2009 |
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13097314 |
|
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61039669 |
Mar 26, 2008 |
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Current U.S.
Class: |
507/240 |
Current CPC
Class: |
C09K 8/03 20130101; C09K
8/62 20130101; C09K 8/60 20130101; C09K 8/035 20130101 |
Class at
Publication: |
507/240 |
International
Class: |
C09K 8/524 20060101
C09K008/524; C09K 8/68 20060101 C09K008/68 |
Claims
1. A method of treating a subterranean region, the method
comprising: providing a eutectic solvent; and introducing the
eutectic solvent into the subterranean region, wherein providing a
eutectic solvent comprises reacting an ammonium compound with a
second compound selected from the group consisting of amines,
amides, carboxylic acids, alcohols, metal halides, and combinations
thereof.
2. The method of claim 1 wherein the ammonium compound is a
quaternary ammonium compound.
3. The method of claim 2 wherein the quaternary ammonium compound
is selected from quaternary ammonium halides.
4. The method of claim 3 wherein the quaternary ammonium compound
is selected from quaternary ammonium chlorides.
5. The method of claim 2, wherein the ammonium compound is selected
from the group consisting of compounds having the structures:
R.sub.1R.sub.2R.sub.3--N R.sub.4Cl and ClR.sub.1R.sub.2R.sub.3--N
R.sub.4Cl, wherein R.sub.1, R.sub.2, and R.sub.3 are selected from
the group consisting of hydrogen and linear or branched alkyl,
aryl, or alkylaryl groups C.sub.xH.sub.y, where
1.ltoreq.x.ltoreq.18 and 3.ltoreq.y.ltoreq.37, and R.sub.4 is
selected from the group consisting of hydrogen and groups having
the structure C.sub.xH.sub.y or C.sub.xH.sub.yOH, where
1.ltoreq.x.ltoreq.18 and 3.ltoreq.y.ltoreq.37.
6. The method of claim 5 wherein R.sub.1, R.sub.2, R.sub.3, and
R.sub.4 are each selected from the group consisting of hydrogen,
methyl-, ethyl-, octadecyl-, phenyl, benzyl- methoxy-, and
ethoxy-groups.
7. The method of claim 5, wherein the ammonium compound is ammonium
chloride.
8. The method of claim 5 wherein the ammonium compound is a
quaternary ammonium chloride, wherein none of R.sub.1, R.sub.2,
R.sub.3, and R.sub.4 is hydrogen.
9. The method of claim 8 wherein the ammonium compound is selected
from the group consisting of chlorcholine chloride and choline
chloride.
10. The method of claim 1 wherein the second compound has a chain
length (C.sub.length) of 1.ltoreq.C.sub.length.ltoreq.18.
11. The method of claim 1 wherein the second compound is urea,
H.sub.2N--CO--NH.sub.2.
12. The method of claim 1 wherein the second compound is a
di-functional amine selected from the group consisting of compounds
with the structure: R.sub.1--(CH.sub.2).sub.x--R.sub.2, wherein
2.ltoreq.x.ltoreq.6, and R.sub.1 and R.sub.2 are selected from the
group consisting of --NH.sub.2, --NHR.sub.3, and --NR.sub.3R.sub.4,
where R.sub.3 and R.sub.4 are selected from alkyl, aryl, and
alkylaryl groups.
13. The method of claim 12 wherein the di-functional amine is
ethylene diamine, H.sub.2N--(CH.sub.2).sub.2--NH.sub.2.
14. A method of treating a subterranean region, the method
comprising: providing an ammonium halide; reacting the ammonium
halide with a hydrogen bond donor to provide a deep eutectic
solvent; and introducing the deep eutectic solvent into a
subterranean region.
15. The method of claim 14 wherein the subterranean region was
previously treated with a drilling fluid or a fracturing fluid
comprising cellulosic material.
16. The method of claim 14 wherein the deep eutectic solvent is
capable of solubilizing up to 30 wt % cellulosic material.
17. The method of claim 14 wherein the deep eutectic solvent is
introduced into the subterranean region as an additive in a
fracturing or other drilling fluid.
18. The method of claim 14 wherein the ammonium halide is selected
from the group consisting of quaternary ammonium chlorides.
19. The method of claim 14 wherein the ammonium halide is selected
from the group consisting of chlorcholine chloride, choline
chloride, ammonium chloride, and combinations thereof.
20. The method of claim 14 wherein the hydrogen bond donor is
selected from amides, carboxylic acids, alcohols and metal
halides.
21. The method of claim 20 wherein the hydrogen bond donor is
selected from amides.
22. The method of claim 21 wherein the hydrogen bond donor is
selected from the group consisting of urea, 1-methyl urea, dimethyl
urea, thiourea, acetamide, and combinations thereof.
23. The method of claim 22 wherein the hydrogen bond donor is
urea.
24. The method of claim 14 further comprising introducing one or
more wash solution into the subterranean following introducing the
deep eutectic solvent into a subterranean region.
25. The method of claim 24 wherein the one or more wash solution is
selected from the group consisting of caustic solutions, acid
solutions, anhydride solutions, water, and combinations
thereof.
26. The method of claim 25 wherein more than one wash solution is
introduced into the subterranean region in series.
27. A method of treating a subterranean region for removal of
cellulosic material therein or prevention of deposition of
cellulosic material therein, the method comprising: reacting a
quaternary ammonium chloride selected from the group consisting of
chlorcholine chloride and choline chloride with a hydrogen bond
donor selected from the group consisting of amides, carboxylic
acids, alcohols and metal halides to produce a deep eutectic
solvent; and introducing the deep eutectic solvent into the
subterranean region, whereby cellulosic material is solubilized in
the deep eutectic solvent.
28. The method of claim 27 wherein the deep eutectic solvent is
introduced into the subterranean region as an additive to a
fracturing fluid comprising cellulosic material.
29. The method of claim 27 wherein the subterranean region was
treated with a fracturing fluid or drilling fluid comprising
cellulosic material prior to introducing the deep eutectic solvent
therein.
30. The method of claim 27 wherein the quaternary ammonium chloride
is chlorcholine chloride and the hydrogen bond donor is urea.
31. The method of claim 27 wherein the quaternary ammonium chloride
is choline chloride and the hydrogen bond donor is urea.
32. The method of claim 27 wherein reacting comprises combining the
quaternary ammonium chloride and the hydrogen bond donor to form a
mixture, and heating the mixture to a temperature of greater than
70.degree. C.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation application which claims
the benefit under 35 U.S.C. .sctn.120 of U.S. patent application
Ser. No. 12/410,662, which claims the benefit under 35 U.S.C.
.sctn.119(e) of U.S. Provisional Patent Application No. 61/039,669
filed Mar. 26, 2008, the disclosures of each of which are hereby
incorporated herein by reference.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
[0002] Not applicable.
BACKGROUND
Field of the Invention
[0003] This invention relates generally to the field of
subterranean drilling and material recovery. More specifically,
this invention relates to the use of deep eutectic solvents and/or
solutions to solubilize cellulose or modified cellulosic polymers
used in subterranean drilling and fracturing operations.
Background of the Invention
[0004] Cellulose is one of the most abundant bio-renewable
materials with a long and well-established technological base.
Cellulose consists of poly-disperse linear glucose polymer chains
which form extremely strong hydrogen-bonded supra-molecular
structures making cellulose insoluble in water and most common
organic liquids. Chemically-modified cellulose is significantly
more soluble in water and imparts viscous properties to solutions
making it useful as an ingredient in drilling and/or fracturing
fluid useful in subterranean drilling operations. In the particular
case of fracturing a formation, causing cracks to form in the
subterranean strata, to allow for the production of hydrocarbon
components with substantially greater ease, it is often necessary
to clean the well bore and resulting fractures to remove cellulosic
material that may have become deposited during the aforementioned
operations and which will impede flow of hydrocarbons through the
fractures and/or production.
[0005] As previously mentioned, cellulose is insoluble in water and
most common organic solvents. Where chemically-modified cellulose
is employed, it is not atypical for all or part of the material to
be hydrolyzed under use conditions reforming the parent compound,
cellulose, which will again become insoluble. Thus, given the
frequency with which cellulosic material is employed in drilling
and fracturing subterranean wells, the development of an additive
and/or solvent for solubilizing cellulose and/or
chemically-modified cellulosic material remains a continuing
challenge in the oil and gas exploration industry.
[0006] In the prior art, room temperature ionic liquids (RTIL) can
solubilize up to 15 wt % cellulose with heating to 150.degree. F.
employing preferably microwave heating. According to Swatlowski, et
al. (U.S. Pat. No. 6,824,599), a solution of cellulose in an ionic
liquid can contain cellulose in an amount of about 5 to about 35
weight percent; more preferably, the cellulose is present at about
5 to 25 weight percent, still more preferably from about 10 to
about 25 weight percent. According to Swatlowski, this solubility
of cellulose in (RTIL), such as [C4mim]Cl, is significantly higher
than can be obtained using other solvents.
[0007] Consequently, there is a need for a method of removing
cellulose and/or cellulosic compounds from a subterranean region.
The method may prevent/minimize the deposition of cellulose and/or
cellulosic compounds on or in the subterranean region or may
solubilize deposited cellulose/cellulosic compounds deposited in a
subterranean region, allowing removal thereof. Desirably, the
method will allow better cost performance and/or improved
toxicological and/or handling properties relative to RTILs, many of
which react adversely with water.
SUMMARY
[0008] A method of treating a subterranean region, the method
comprising: providing a eutectic solvent; and introducing the
eutectic solvent into the subterranean region. In embodiments,
providing a eutectic solvent further comprises reacting an ammonium
compound with a second compound selected from the group consisting
of amines, amides, carboxylic acids, alcohols, metal halides, and
combinations thereof. In embodiments, the ammonium compound is a
quaternary ammonium compound. The quaternary ammonium compound can
be selected from quaternary ammonium halides. The quaternary
ammonium compound can be selected from quaternary ammonium
chlorides.
[0009] In embodiments, the ammonium compound is selected from the
group consisting of compounds having the structures:
R.sub.1R.sub.2R.sub.3--N R.sub.4Cl and Cl R.sub.1R.sub.2R.sub.3--N
R.sub.4Cl, wherein R.sub.1, R.sub.2, and R.sub.3 are selected from
the group consisting of hydrogen and linear or branched alkyl,
aryl, or alkylaryl groups C.sub.xH.sub.y, where
1.ltoreq.x.ltoreq.18 and 3.ltoreq.y.ltoreq.37, and R.sub.4 is
selected from the group consisting of hydrogen and groups having
the structure C.sub.xH.sub.y or C.sub.xH.sub.yOH, where
1.ltoreq.x.ltoreq.18 and 3.ltoreq.y.ltoreq.37. In embodiments,
R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are each selected from the
group consisting of hydrogen, methyl-, ethyl-, octadecyl-, phenyl,
benzyl- methoxy-, and ethoxy- groups. In embodiments, the ammonium
compound is ammonium chloride. In embodiments, the ammonium
compound is a quaternary ammonium chloride, wherein none of
R.sub.1, R.sub.2, R.sub.3, and R.sub.4 is hydrogen. In embodiments,
the ammonium compound is selected from the group consisting of
chlorcholine chloride and choline chloride.
[0010] The second compound may have a chain length (C.sub.length)
of 1.ltoreq.C.sub.length.ltoreq.18. In embodiments, the second
compound is urea, H.sub.2N--CO--NH.sub.2. In embodiments, the
second compound is a di-functional amine selected from the group
consisting of compounds with the structure:
R.sub.1--(CH.sub.2).sub.x--R.sub.2, wherein 2.ltoreq.x.ltoreq.6,
and R.sub.1 and R.sub.2 are selected from the group consisting of
--NH.sub.2, --NHR.sub.3, and --NR.sub.3R.sub.4, where R.sub.3 and
R.sub.4 are selected from alkyl, aryl, and alkylaryl groups. In
embodiments, the di-functional amine is ethylene diamine,
H.sub.2N--(CH.sub.2).sub.2--NH.sub.2.
[0011] Also disclosed is a method of treating a subterranean
region, the method comprising: providing an ammonium halide;
reacting the ammonium halide with a hydrogen bond donor to provide
a deep eutectic solvent; and introducing the deep eutectic solvent
into a subterranean region. In embodiments, the subterranean region
was previously treated with a drilling fluid or a fracturing fluid
comprising cellulosic material. In embodiments, the deep eutectic
solvent is capable of solubilizing up to 30 wt % cellulosic
material. In embodiments, the deep eutectic solvent is introduced
into the subterranean region as an additive in a fracturing or
other drilling fluid.
[0012] In embodiments, the ammonium halide is selected from the
group consisting of quaternary ammonium chlorides. The ammonium
halide may be selected from the group consisting of chlorcholine
chloride, choline chloride, ammonium chloride, and combinations
thereof. In embodiments, the hydrogen bond donor is selected from
amides, carboxylic acids, alcohols and metal halides. In
embodiments, the hydrogen bond donor is selected from amides. The
hydrogen bond donor may be selected from the group consisting of
urea, 1-methyl urea, dimethyl urea, thiourea, acetamide, and
combinations thereof. In embodiments, the hydrogen bond donor is
urea.
[0013] In embodiments, the method further comprises introducing one
or more wash solution into the subterranean following introducing
the deep eutectic solvent into a subterranean region. The one or
more wash solution can be selected from the group consisting of
caustic solutions, acid solutions, anhydride solutions, water, and
combinations thereof. In embodiments, more than one wash solution
is introduced into the subterranean region in series.
[0014] Also disclosed is a method of treating a subterranean region
for removal of cellulosic material therein or
minimization/prevention of deposition of cellulosic material
therein, the method comprising: reacting a quaternary ammonium
chloride selected from the group consisting of chlorcholine
chloride and choline chloride with a hydrogen bond donor selected
from the group consisting of amides, carboxylic acids, alcohols and
metal halides to produce a deep eutectic solvent; and introducing
the deep eutectic solvent into the subterranean region, whereby
cellulosic material is solubilized in the deep eutectic solvent. In
embodiments, the deep eutectic solvent is introduced into the
subterranean region as an additive to a fracturing fluid comprising
cellulosic material. In embodiments, the subterranean region was
treated with a fracturing fluid or drilling fluid comprising
cellulosic material prior to introducing the deep eutectic solvent
therein. In embodiments, the quaternary ammonium chloride is
chlorcholine chloride and the hydrogen bond donor is urea. In
embodiments, the quaternary ammonium chloride is choline chloride
and the hydrogen bond donor is urea. Reacting may comprise
combining the quaternary ammonium chloride and the hydrogen bond
donor to form a mixture, and heating the mixture to a temperature
of greater than 70.degree. C.
[0015] The foregoing has outlined rather broadly the features and
technical advantages of the invention in order that the detailed
description of the invention that follows may be better understood.
Additional features and advantages of the invention will be
described hereinafter that form the subject of the claims of the
invention. It should be appreciated by those skilled in the art
that the conception and the specific embodiments disclosed may be
readily utilized as a basis for modifying or designing other
structures for carrying out the same purposes of the invention. It
should also be realized by those skilled in the art that such
equivalent constructions do not depart from the spirit and scope of
the invention as set forth in the appended claims.
BRIEF DESCRIPTION OF THE DRAWING
[0016] For a more detailed description of the preferred embodiment
of the present invention, reference will now be made to the
accompanying drawing, wherein:
[0017] FIG. 1 is a flow diagram of a method of solubilizing
cellulose and/or cellulosic materials during drilling and/or
fracturing operations according to an embodiment of this
disclosure.
NOTATION AND NOMENCLATURE
[0018] As used herein, the terms `cellulosic` and `cellulosic
material` are used to refer to materials of, relating to, or made
from cellulose, including chemically-modified cellulose.
[0019] As used herein, the term `deep eutectic solvent` is used to
refer to a type of ionic solvent with special properties, the ionic
solvent comprising a mixture which forms a eutectic with a melting
point significantly lower than that of its individual components.
Such mixtures of proton donors and halide salts are relatively
simple to prepare in a pure state. Deep eutectic solvents are
non-reactive with water, many are biodegradable, and the
toxicological properties of the components are well
characterized.
DETAILED DESCRIPTION
[0020] I. Overview. This invention relates to the use of deep
eutectic solvents (DES) in solubilizing/removing cellulose or
chemically-modified cellulosic polymers used in subterranean
drilling operations such as fracturing. As discussed below, deep
eutectic solvents useful as cellulose solvents include choline
chloride or chlorcholine chloride reacted with amides, amines,
carboxylic acids, alcohols and/or metal halides. In embodiments of
the disclosed method, a DES is pumped downhole after fracturing
operations to remove cellulosic material used to thicken fracturing
fluids which is left behind in the fractures, on the face of the
formation, along the wellbore, etc. The DES can be used alone or in
a sequential treatment protocol, for example, DES may be introduced
into a subterranean region, followed by introduction thereto of one
or more of water, caustic, acid or anhydride as a flush or
wash.
[0021] Herein disclosed is a method of treating a subterranean
region. FIG. 1 is a flow diagram of a method I for treating a
subterranean region. Method I is utilized to solubilize cellulose
and/or chemically-modified cellulosic polymers used in drilling and
fracturing operations. The method may be used to remove cellulose
or chemically-modified cellulosic polymers within a subterranean
region, to promote removal thereof. Such cellulose may be found in
the wellbore as a result of subterranean drilling and fracturing
operations. For example, cellulosic materials are typically used as
viscosity modifiers in water-based drilling and fracturing fluids.
Such cellulosic materials can be selected from the group containing
guar, cellulose and chemically-modified celluloses such as
carboxy-methylcellulose, hydroxyl-ethylcellulose and the like.
[0022] Method I comprises providing a eutectic solvent at 100 and
introducing the eutectic solvent into the wellbore at 200, to
solubilize and/or remove cellulosic materials therein. The method
may further comprise introducing post-treatment solution into the
wellbore at 300. As illustrated in FIG. 1, providing a eutectic
solvent 100 comprises selecting an ammonium compound at 110 and
reacting the ammonium compound to form eutectic solvent at 120.
[0023] II. Eutectic Solvent. According to this disclosure, a Deep
Eutectic Solvents or solution (DES) is formed by complexing an
ammonium compound, for example N-(2-hydroxyethyl)
trimethyl-ammonium chloride (choline chloride), with a
hydrogen-bond donor (HBD) such as carboxylic acids, amines, amides
and alcohols. These liquids have physical and solvent properties
that are similar to ionic liquids formed from discrete ions and are
easy to produce by simply mixing common commodity chemicals such as
choline chloride and carboxylic acids or amides as further
discussed hereinbelow.
[0024] Deep eutectic solvents can be designed and improved upon
using Hole Theory. In Hole Theory, the viscosity of a fluid is
related to its free volume and the probability of finding holes of
suitable dimension for solvent molecules/ions to enter is related
to the surface tension of the fluid. To improve ionic mobility, it
is necessary to study the distribution of voids in the liquid. The
probability P, of finding a hole of radius r, in a given liquid
depends on the following equation:
Pdr=(16/15 .pi.)a.sup.7/2r.sup.6e.sup.-ar2dr, (1)
wherein a=4.pi..delta./kT, .delta. is the surface tension, k is the
Boltzmann constant, and T the absolute temperature (K). Further,
the value of (16/15 .pi.) equals 0.602. Equation (1) indicates that
it is possible to increase the average size of the voids in a
solvent/solution by decreasing the surface tension. The expected
affect would be the higher solubility of cellulose or
chemically-modified cellulosic material in the resulting
solution.
[0025] Ammonium Compound Method I comprises providing a eutectic
solvent 100. Providing a eutectic solvent 100 comprises selecting
an ammonium compound 110 and reacting the ammonium compound 120 to
produce a eutectic solvent. In applications, the ammonium compound
is an ammonium halide. In embodiments, the ammonium compound is an
ammonium chloride. In embodiments, the ammonium compound is
ammonium chloride. In applications, the ammonium compound is a
quaternary ammonium compound. In applications, the quaternary
ammonium compound is selected from the group consisting of
quaternary ammonium halides. In applications, the quaternary
ammonium halide is selected from the group consisting of quaternary
ammonium chlorides.
[0026] In embodiments, the ammonium compound is selected from the
group consisting of the ammonium chlorides having the
structure:
(R.sub.1R.sub.2R.sub.3)--N.sup.+--R.sub.4--OH Cl.sup.- (2)
[0027] wherein R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are each
selected from the group consisting of H and C.sub.xH.sub.y, wherein
1.ltoreq.x.ltoreq.18 and 3.ltoreq.y.ltoreq.37. R.sub.1, R.sub.2,
R.sub.3 and R.sub.4 can be branched or linear and can be alkyl,
aryl or alkylaryl. In embodiments, R1, R2, R3, and R4 are not
hydrogen, and the ammonium compound is a quaternized ammonium
chloride having the structure as in Eq. (2). In embodiments,
R.sub.1, R.sub.2, R.sub.3, R.sub.4 or any combination thereof is
selected from the group consisting of methyl-, ethyl-, octadecyl-,
phenyl, benzyl- and combinations thereof. In applications, R.sub.1,
R.sub.2 and R.sub.3 are methyl, and R.sub.4 is ethyl. In this
embodiment, the ammonium compound is the quaternary ammonium
compound N-(2-hydroxyethyl) trimethyl-ammonium chloride
(CH.sub.3).sub.3--N.sup.+--(CH.sub.2CH.sub.2OH)Cl.sup.-, also known
as choline chloride or vitamin B4.
[0028] In embodiments, the ammonium compound is selected from the
group consisting of ammonium chlorides having the structure:
(R.sub.1R.sub.2R.sub.3)--N.sup.+--R.sub.4Cl (3)
[0029] wherein R.sub.1,R.sub.2, R.sub.3 and R.sub.4 may be the same
or different, and can be hydrogen or branched or linear alkyl,
alkylaryl, or aryl groups. In applications, R.sub.1, R.sub.2,
R.sub.3 and R.sub.4 are selected from the group consisting of H and
C.sub.xH.sub.y, wherein 1.ltoreq.x.ltoreq.18 and
3.ltoreq.y.ltoreq.37. In applications, R.sub.1, R.sub.2 and R.sub.3
are selected from the group consisting of methyl-, ethyl-,
octadecyl-, phenyl, benzyl-, methoxy-, ethoxy-, and the like. In
applications, R.sub.1, R.sub.2 and R.sub.3 are methyl and R.sub.4
is ethyl. In such an embodiment, the ammonium chloride may be the
quaternary ammonium chloride 2-chloro-N,N,N-trimethylethanaminium.
In embodiments, R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are
hydrogen, and the ammonium compound is ammonium chloride.
[0030] In embodiments, the ammonium compound is selected from the
group consisting of chloro-substituted ammonium chlorides having
the structure:
Cl.sup.-(R.sub.1R.sub.2R.sub.3)--N.sup.+--R.sub.4Cl (4)
wherein R.sub.1,R.sub.2, R.sub.3 and R.sub.4 may be the same or
different, and can be hydrogen or branched or linear alkyl,
alkylaryl, or aryl groups. In applications, R.sub.1, R.sub.2,
R.sub.3 and R.sub.4 are selected from the group consisting of
methyl-, ethyl-, octadecyl-, phenyl, benzyl-, methoxy-, ethoxy-,
and the like. In applications, R.sub.1, R.sub.2 and R.sub.3 are
methyl groups and R.sub.4 is an ethyl group. In this embodiment,
the ammonium compound is the quaternary ammonium chloride
chlorcholine chloride, [2-chloroethyl-trimethyl-azanium chloride,
Cl.sup.-(CH.sub.3).sub.3N.sup.+CH.sub.2CH.sub.2Cl].
[0031] In embodiments, the ammonium compound is selected from the
group consisting of ammonium chloride, choline chloride
[N-(2-Hydroxyethyl) trimethyl ammonium chloride,
(CH.sub.3).sub.3-N.sup.+--CH.sub.2CH.sub.2OHCl], chlorcholine
chloride, and 2-chloro-N,N,N-trimethylethanaminium. In embodiments,
the ammonium compound is a quaternary ammonium compound selected
from the group consisting of chlorcholine chloride, choline
chloride, 2-chloro-N,N,N-trimethylethanaminium, and combinations
thereof.
[0032] Second Compound Reacting the ammonium compound to produce a
eutectic solvent at 120 comprises reacting the ammonium compound
with a second compound to produce a deep eutectic solvent. The
second compound is a hydrogen bond donor (HBD). In applications,
the second compound is selected from amines, amides, carboxylic
acids, alcohols and metal halides. In applications, the second
compound has a chain length (C.sub.length) in the range of from 1
to 18; from 1 to 10; or from 1 to 8.
[0033] In applications, the second compound is an amine. In
applications, the second compound is selected from di-functional
amines. In applications, the second compound is selected from the
group consisting of compounds with the structure:
R.sub.1--(CH.sub.2).sub.x--R.sub.2, (5)
wherein R.sub.1 and R.sub.2 are --NH.sub.2, --NHR.sub.3, or
--NR.sub.3R.sub.4 and 2.ltoreq.x.ltoreq.6. In applications, the
di-functional amine compound is ethylene diamine,
H.sub.2N--(CH.sub.2).sub.2--NH.sub.2.
[0034] In applications, the second compound is an amide. In
applications, the second compound is selected from the group
consisting of compounds with the structure:
R--CO--NH.sub.2, (6)
wherein R is H, NH.sub.2, CH.sub.3, or CF.sub.3. In applications, R
is NH.sub.2, and the compound is urea, H.sub.2N--CO--NH.sub.2. In
applications, the second compound is selected from 1-methyl urea,
(CH.sub.3NHCONH.sub.2), 1,3-dimethylurea (CH.sub.3NHCONHCH.sub.3),
thiourea ((NH.sub.2).sub.2CS), and acetamide (CH.sub.3CONH).
[0035] In specific embodiments, the deep eutectic solvent (DES) is
a solvents/solution of a di-functional amine and N-(2-hydroxyethyl)
trimethyl-ammonium chloride, generically choline chloride.
[0036] As discussed further in Examples 1 and 2 hereinbelow,
reacting the ammonium compound may comprise combining the ammonium
compound with an amide (e.g., urea) at a 1:2 mole ratio. The
mixture is heated, with stirring, and allowed to react until a
clear, viscous, uniform solution is formed. The mixture may be
heated to a temperature greater than 80.degree. C., greater than
90.degree. C. or greater than 100.degree. C. If an exotherm is
observed, external heating may be discontinued until the exotherm
subsides. If the reaction mixture is still not completely clear and
uniform, the reaction mixture may be again externally heated to a
temperature of greater than 80.degree. C., greater than 90.degree.
C. or greater than 100.degree. C. until reaction is complete. The
liquid is then allowed to cool to room temperature. Cooling to room
temperature may comprise cooling at a rate of less than 1.degree.
C./min.
[0037] In applications, the second compound is selected from
carboxylic acids. In applications, the second compound is selected
from mono- and di-functional organic alkyl and aryl acids. In
applications, the second compound is a mono-functional carboxylic
acid. In embodiments, the ammonium compound is reacted with the
mono-carboxylic acid at a 1:2 molar ratio of ammonium compound to
mono-functional carboxylic acid to form the eutectic solvent. In
applications, the mono-carboxylic acid is selected from
phenylpropionic acid (C.sub.6H.sub.6CH.sub.2CH.sub.2CO.sub.2H),
phenylacetic acid (C.sub.6H.sub.6CH.sub.2CO.sub.2H), and
combinations thereof.
[0038] In applications, the second compound is a di-functional
carboxylic acid. As discussed in Example 3 hereinbelow, in such
embodiments, the ammonium compound may be reacted with the
di-functional carboxylic acid at a 1:1 molar ratio. In
applications, the second compound is selected from oxalic acid
(HO.sub.2CCO.sub.2H), malonic acid (HO.sub.2CCH.sub.2CO.sub.2H),
succinic acid (HO.sub.2CCH.sub.2CH.sub.2CO.sub.2H), and
combinations thereof.
[0039] In embodiments, the second compound is selected from tris or
tri-functional carboxylic acids. In such embodiments, the solvent
may be formed at a 30-35 mol % acid. Suitable tri-functional
carboxylic acids include citric acid and tricarballylic acid.
[0040] In applications, the second compound is a metal halide. The
metal halide may be selected from the group consisting of aluminum
chloride, zinc chloride, tin chloride, iron chloride, and
combinations thereof. The latter three molten product salts have
the advantage that they are not water sensitive, although they are
found to be, in general, more viscous than the aluminum derivative.
The depression of the freezing points may be as much as 190.degree.
C.
[0041] C. Reacting Ammonium Compound with Second Compound As
discussed further in Examples 1 and 2 hereinbelow, reacting the
ammonium compound may comprise combining the ammonium compound
(e.g., quaternary ammonium halide) with an amide (e.g., urea) at a
67 mole percent amide; with a mono-functional carboxylic acid at a
67 mole percent mono-functional carboxylic acid; with a
di-functional carboxylic acid at 50 mole percent di-functional
carboxylic acid; with a tri-carboxylic acid at 30-35 mole percent;
or with metal halide at a 30-67 mole percent metal halide,
depending upon the charge on the metal halide. For example,
ZnCl.sub.2 reacts in a different ratio than FeCl.sub.3. In the
specific case of ZnCl.sub.2 the reaction yields
[(CHCl)(ZnCl.sub.2).sub.2] which reflects a reaction ratio of 1:2
or 67 mole percent metal or zinc chloride.
[0042] The mixture comprising the ammonium compound and second
compound is heated, with stirring, and allowed to react until a
clear, viscous, uniform solution is formed. The mixture may be
heated to a temperature greater than 80.degree. C., greater than
90.degree. C. or greater than 100.degree. C. If an exotherm is
observed, external heating may be discontinued until the exotherm
subsides. If the reaction mixture is still not completely clear and
uniform, the reaction mixture may be again externally heated to a
temperature of greater than 80.degree. C., greater than 90.degree.
C. or greater than 100.degree. C. until reaction is complete. The
liquid is then allowed to cool to room temperature. Cooling to room
temperature may comprise cooling at a rate of less than 1.degree.
C./min.
[0043] The DES may have a solubility for cellulose of at least 30
weight %, at least 40 weight %, at least 45 weight %, at least 50
weight %, or at least 55 weight %.
[0044] III. Introducing the Eutectic Solvent into Subterranean
Region. The method further comprises introducing the eutectic
solvent into a subterranean region 200. The eutectic solvent may be
introduced into a subterranean region such as a wellbore, casing,
fracture or face of a formation. The subterranean region may
contain therein cellulose or cellulosic material to be solubilized
via the eutectic solvent and thus may be removed from the
subterranean region. Cellulose or cellulosic materials may be
present in the subterranean region as a result of fracturing and/or
mud thickening operations, for example, utilized in a drilling
operation. The cellulose or chemically-modified cellulose may have
been introduced into the subterranean region as a component of a
drilling fluid or a fracturing fluid. In specific applications, the
DES is introduced into a formation which has been fractured
utilizing a fracturing fluid comprising cellulose in order to clean
the well bore and the resulting fractures and remove any cellulosic
materials that may have deposited during the fracturing operation
and now hinder production from the fractures.
[0045] In other applications, the DES is introduced into the
subterranean region as a component of a drilling fluid (i.e., a
fracturing fluid, drilling mud, or other drilling fluid) which
further comprises cellulose or cellulosic materials. In this
manner, the DES is utilized as an additive to maintain solubility
of the cellulose or cellulosic material (e.g., chemically modified
cellulose which may, in the absence of the DES, hydrolyze to
cellulose, becoming insoluble in the drilling fluid),
preventing/minimizing deposition therein.
[0046] The DES is introduced into the subterranean region at
conditions known to those of skill in the art to be suitable for
the introduction of fluids downhole. In applications, the DES is
introduced into the subterranean region at a temperature in the
range of from about 50.degree. C. to about 150.degree. C.
Alternatively, a temperature in the range of from about 65.degree.
C. to about 135.degree. C. In applications, the DES is pumped into
the subterranean region at a pressure in the range of from about
500 to about 25,000 psig. Alternatively, a pressure in the range of
from about 1,000 to about 10,000 psig. Alternatively, a pressure in
the range of from about 1,000 to about 5,000 psig.
[0047] IV. Introducing Post-Treatment Solution into Subterranean
Region. The method I may further comprise introducing
post-treatment solution into the subterranean region 300. In
instances, the DES is used alone, with no post-treatment. In
applications, the Deep Eutectic Solvents (DES) are used and a wash
is subsequently introduced into the subterranean region. The wash
may be selected from a water wash, a caustic wash, an anhydride
wash, an acid wash, or a combination thereof. A caustic wash may be
selected from sodium hydroxide and potassium hydroxide. An
anhydride wash may comprise acetic anhydride.
[0048] While the preferred embodiments of the invention have been
shown and described, modifications thereof can be made by one
skilled in the art without departing from the spirit and teachings
of the invention. The embodiments described and the examples
provided herein are exemplary only, and are not intended to be
limiting. Many variations and modifications of the invention
disclosed herein are possible and are within the scope of the
invention. Accordingly, the scope of protection is not limited by
the description set out above, but is only limited by the claims
which follow, that scope including all equivalents of the subject
matter of the claims.
[0049] To further illustrate various illustrative embodiments of
the present invention, the following examples are provided.
EXAMPLES
Example 1
Synthesis of Choline Chloride/Amide Deep Eutectic Solvent (DES)
[0050] Urea which has a melting point of 133.degree. C.
(271.degree. F.) is combined with N-(2-hydroxyethyl)
trimethyl-ammonium chloride (choline chloride) which has a melting
point of 302.degree. C. (575.degree. F.) in a 2:1 molar ratio. One
(1) mole (139.6 grams) of choline chloride, [N-(2-hydroxyethyl)
trimethylammonium chloride,
(CH.sub.3).sub.3N.sup.+CH.sub.2CH.sub.2OH]Cl.sup.-, FW=139.6 g/mol]
is employed as a dry powder or flake and is added to 2 moles of
urea, an amide, [120 grams [(NH.sub.2).sub.2CO, FW=60 g/mol]. With
stirring, the dry mixture is heated to 100.degree. C. (212.degree.
F.) until the solids have all been dissolved to affect reaction and
remove any latent water in either component. The reaction is
continued until a clear, viscous, uniform solution is formed. If an
exotherm is observed, external heating is discontinued until the
exotherm subsides. If the reaction solution is still not completely
clear and uniform, the reaction mixture may again be heated
externally to 100.degree. C. (212.degree. F.) until the reaction is
complete. The liquid is then allowed to cool to room temperature at
a rate no faster than 1.degree. C./min. The yield is quantitative
and the product has a melting point of 12.degree. C. (-53.6.degree.
F.). The variables for this deep eutectic solvent are:
P=7.63.times.10.sup.-3; .eta..sub.calc=11 cP; V.sub.m=210.1
cm.sup.3mol.sup.-1; V.sub.free=9.1%; and E.sub..eta.=58
kJmol.sup.-1.
[0051] Numerous other choline chloride (ChCl.sup.-)/amide compounds
can be synthetically prepared employing the method detailed above
including but not limited to 1-methyl urea (CH.sub.3NHCONH.sub.2,
m. p.=29.degree. C.), 1,3-dimethylurea (CH.sub.3NHCONHCH.sub.3,
m.p.=70.degree. C.), thiourea ((NH.sub.2).sub.2CS, m.p.=69.degree.
C.), acetamide (CH.sub.3CONH.sub.2, m.p.=51.degree. C.) and
others.
Example 2
Synthesis of Chlorcholine Chloride/Amide Deep Eutectic Mixtures
(DES)
[0052] Chlorcholine chloride
[Cl.sup.-(CH.sub.3).sub.3N.sup.+CH.sub.2CH.sub.2Cl), 12.96 g, 0.082
mol) is added to urea (9.78 g., 0.163 mol) and the mixture heated
to 80.degree. C. (176.degree. F.) with stirring for approximately
30 minutes. A clear, viscous, uniform solution is formed and
allowed to cool to room temperature at a rate of approximately
1.degree. C./min. The liquid can be maintained for at least a month
when protected against moisture.
[0053] As with choline chloride in Example 1, numerous chlorcholine
chloride/amide derivatives can be prepared. The reaction time is
reduced due to the higher reactivity coefficient of the
chloro-derivative.
Example 3
Synthesis of Choline Chloride/Carboxylic Acid Deep Eutectic
Mixtures (DES)
[0054] Based on the method presented in Example 1, it becomes
apparent that a eutectic is formed at a composition of 67% mol
urea. From this data, it can be inferred that to form the eutectic
two carboxylic acid molecules are required to complex each chloride
ion. Therefore, a mono-functional carboxylic acid molecule reacts
with ChCl.sup.- on a 1:2 molar basis as is the case with
phenylpropionic acid (C.sub.6H.sub.6CH.sub.2CH.sub.2CO.sub.2H) and
phenylacetic acid (C.sub.6H.sub.6CH.sub.2CO.sub.2H).
[0055] Eutectics formed with di-functional carboxylic acids occur
at a 50% mol ratio strongly suggesting a 1:1 complex between the
acid and the chloride ion or else said acids act as bridging
molecules between neighboring chloride ions. Such would be the case
when considering oxalic acid (HO.sub.2CCO.sub.2H), malonic acid
(HO.sub.2CCH.sub.2CO.sub.2H) and succinic acid
(HO.sub.2CCH.sub.2CH.sub.2CO.sub.2H), for example.
[0056] The freezing point depression, when compared to an ideal
mixture of the two components, for [ChCl.sup.-.oxalic acid] is
212.degree. C. as compared to [ChCl.sup.-.(urea).sub.2] which was
178.degree. C. but not as large as [ChCl.sup.-.(ZnCl.sub.2).sub.2]
systems 272.degree. C., wherein covalent bonds are formed.
[0057] Eutectics formed with tris- or tri-functional carboxylic
acids occur at a 30-35% mol acid. Eutectics containing citric and
tricarballylic exhibit the rheology of gels and are assumed to
exhibit extensive bridging between acid groups and their
neighboring chloride ions.
[0058] The melting point of eutectics formed by the reaction of 1
mol of choline chloride (ChCl.sup.-) and 1 mol of oxalic acid is
34.degree. C.; 1 mol of ChCl.sup.- and 1 mol of malonic acid is
10.degree. C.; and 1 mol of ChCl.sup.- and 1 mol of succinic acid
is 71.degree. C. The melting point of the choline chloride/citric
acid eutectic is 69.degree. C. and the choline
chloride/tricarballylic acid eutectic is 90.degree. C.
Example 4
Dissolution of Cellulose with Ionic Liquids (Comparative
Example)
[0059] In a typical procedure developed by Swatloski, et al. (U.S.
Pat. No. 6,824,599), to prepare a 10 wt % solution, 0.5-1.0 grams
of fibrous cellulose was placed in a glass vial and [C.sub.4mim]Cl
ionic liquid (10 grams) was added as a liquid at 70.degree. C. (a
temperature above its melting point). The vial was loosely capped,
placed in a microwave oven and heated with 3-5 sec. pulses at full
power. Between pulses, the vial was removed, shaken or vortexed and
replaced in the oven. A clear, colorless, viscous solution was
obtained. Although solutions containing 5-10 wt % cellulose are
more easily prepared, solutions containing up to 25 wt % cellulose
can be formed only as viscous pastes.
[0060] [C.sub.4mim]Cl ionic liquids are comprised of [C.sub.4mim] a
1-butyl-3-methylimidazolium cation and Cl.sup.-, a chloride ion. In
comparing the chemicals employed, the highest cellulose solubility
employing an ionic liquid and microwave heating is 25% and the
product is a paste.
Example 5
Dissolution of Cellulose with Deep Eutectic Solvents (DES)
[0061] The dissolution of various cellulosic polymers including but
not limited to xanthan gum, cellulose fibers, modified guar gum,
carboxymethyl tamarind and sodium carboxymethyl cellulose were
tested employing choline chlorideurea eutectics. To a small vial, a
50:50 mixture of the selected polymer and the eutectic solvent of
choice was added and the sample placed into a standard convection
oven at temperatures between 65-135.degree. C. In all cases, the
cellulosic polymers mentioned above were found to be soluble at the
lowest temperature tested 65.degree. C. (.about.150.degree. F.).
When allowed to cool to room temperature, a clear, viscous solution
or gel was found to have been formed.
[0062] Employing a choline chloride/urea deep eutectic solvent, 50
wt % solubility is not at all unreasonable, utilizing reasonable
heating techniques. The resulting product at temperature is
liquid.
[0063] While the preferred embodiments of the invention have been
shown and described, modifications thereof can be made by one
skilled in the art without departing from the spirit and teachings
of the invention. The embodiments described and the examples
provided herein are exemplary only, and are not intended to be
limiting. Many variations and modifications of the invention
disclosed herein are possible and are within the scope of the
invention. Accordingly, the scope of protection is not limited by
the description set out above, but is only limited by the claims
which follow, that scope including all equivalents of the subject
matter of the claims.
[0064] The discussion of a reference herein is not an admission
that it is prior art to the present invention, especially any
reference that may have a publication date after the priority date
of this application. The disclosures of all patents, patent
applications, and publications cited herein are hereby incorporated
herein by reference in their entirety, to the extent that they
provide exemplary, procedural, or other details supplementary to
those set forth herein.
* * * * *