US20080200351A1

US20080200351A1 - Method of recycling fracturing fluids using a self-degrading foaming composition

Info

Publication number: US20080200351A1
Application number: US12/148,638
Authority: US
Inventors: Manilal S. Dahanayake; Subramanian Kesavan; Allwyn Colaco
Original assignee: Individual
Current assignee: Individual
Priority date: 2005-04-06
Filing date: 2008-04-21
Publication date: 2008-08-21
Also published as: DK1866519T3; WO2006108161A3; CA2603960C; CA2826313C; CA2826313A1; US7404442B2; EP1866519A4; EP1866519A2; WO2006108161A2; CA2603960A1; US20060260815A1; EP1866519B1

Abstract

A method of fracturing a subterranean zone penetrated by a well bore preparing a foamed fracturing fluid containing a self-degrading foaming composition with a mixture of anionic surfactant and nonionic surfactant, and a composition thereof. The fracturing fluid containing self-degrading foaming composition forms a substantially less stable foam when the foamed fracturing fluid is recovered during reclaim.

Description

CROSS REFERENCE TO RELATED APPLICATION

This application is a divisional application of U.S. application Ser. No. 11/399,223 filed Apr. 06, 2006.

BACKGROUND OF THE INVENTION

1. Field of the Invention
This invention generally relates to method of recycling foamed fracturing fluids used in fracturing subterranean formations in oil and gas wells. More specifically, the invention relates to a self-degrading foaming composition that enhances the recycling of foamed fracturing fluids due to its defoaming character during reclaim of the fluid.
2. Description of the Related Art
Natural resources such as gas, oil, minerals, and water residing in a subterranean formation can be recovered by drilling wells into the formation. The fluids in the subterranean formation are driven into the wells by, for example, pressure gradients that exist between the formation and the wells, the force of gravity, displacement of the fluids using pumps or the force of another fluid injected into the wells. The production of such fluids is commonly increased by hydraulically fracturing the subterranean formations. That is, a viscous fracturing fluid is pumped into a well to a subterranean formation at a rate and a pressure sufficient to form fractures that extend into the formation, providing additional pathways through which the fluids can flow to the wells.
The fracturing fluid is usually a water-based fluid containing a gelling additive to increase the viscosity of the fluid. The gelling additive thus reduces leakage of liquid from the fractures into the subterranean formation and improves proppant suspension capability. The gelling additive is commonly a polymeric material that absorbs water and forms a gel as it undergoes hydration.
In certain applications one or more foaming surfactants are added to the fracturing fluid. A gas is mixed with the fracturing fluid to produce a foamed fracturing fluid, thus ensuring that the pressure exerted by the fracturing fluid on the subterranean formation exceeds the fracture gradient (psi/ft.) to create the fracture. The foamed fracturing fluid is injected by foaming the fracturing fluid with nitrogen or carbon dioxide. The foaming composition containing one or more surfactants facilitates the foaming and stabilization of the foam produced when the gas is mixed with the fracturing fluid.
After a fracturing fluid has been used to form fractures in a subterranean formation, it is usually returned to the surface for disposal or recycle. When fluid is returned, it is desirable to have a fluid that does not foam. Also, it would be desirable to have the ability to recycle the fracturing fluid to form additional fractures in the same subterranean formation or to form fractures in one or more different subterranean formations. Frequently, foamed fracturing fluids are not suitable for recycling. In the recycling operations it is desirable to have a fracturing fluid to be without foam for ease of operation. These recycling operations require addition of defoamer to the fracturing fluids to decrease the foaming and ease of operation.
Alternatively, the pH of the fracturing fluid may be changed to obtain defoaming during recycling conditions. However, this approach is susceptible to pH fluctuations and if the pH is changed back to the high foaming state, the fracturing fluid will foam again and severely hinder the ease of recycling operation. U.S. Patent Application No: 2004/02006616 to Chatterji et al., Oct. 14, 2004, describes cationic tertiary alkyl amine ethoxylates and its mixtures with anionic and amphoteric compounds which can be foamed at pH greater than 9 and defoamed at pH less than 6 or foamed at pH less than 6 and defoamed at pH greater than 9.
U.S. Patent Application 2003/0207768 to England et. al., Nov. 6, 2003, describes a foaming well treatment fluid comprising an amphoteric surfactant. The objective of this patent is to use surfactants that have good wetting characteristics in the presence of coal and be effective foaming agents. Also the recycling of the foamed fracturing fluid is obtained by lowering the pH of the fluid. However such systems are susceptible to pH variations. In addition, adjustment of pH involves additional steps in the recycling operations and usually pH adjustment involves addition of acids that are not desired in terms of environmental acceptability.
It is desirable that the fracturing fluid does not foam in the fracturing blender or at any stage before it without the change of pH and/or addition of defoamer. Further, a foaming composition that foams initially but will be substantially less in foam stability after time is highly desirable for recycling operations. Typically a foaming composition that will foam initially and after about 24 hours to have low foam stability is suitable to facilitate processing.
Accordingly, there is provided a foamed fracturing fluid comprised of water, a self-degrading foaming composition comprising one or more surfactant. The foamed composition will foam initially but will have reduced foam stability when the fracturing fluid is recovered during flowback.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide a method of fracturing a subterranean zone penetrated by a well bore comprising:

(a) preparing a foamed fracturing fluid comprised of water, a self-degrading foaming composition comprising a mixture of anionic surfactant and nonionic surfactant, and sufficient gas to form a foam when fracturing fluid is injected; and
(b) contacting said subterranean zone with said foamed fracturing fluid under conditions effective to create at least one fracture therein,
- wherein the self-degrading foaming composition forms a substantially less stable foam when the fracturing fluid is recovered during recycling.

It has been unexpectedly found that the use of foaming composition comprising an anionic surfactant and a nonionic surfactant will foam initially but will not foam after aging compared to the conventional foaming agents used in the recycle operations. The foamed fracturing fluid contains a gelling agent. This foamed fracturing fluid does not depend on the change of pH for defoaming during recycling of the fracturing fluid.
Another object of this invention to introduce a foaming composition in the fracturing fluid, which does not foam in the fracturing blender or any stage before it.
It is still another object of the invention to have a foamed fracturing fluid where the addition of a defoamer is not required to decrease the foam during the recycle operations.
A further object of the invention to obtain a foaming composition and a foamed fracturing fluid independent on significantly induced pH changes by addition of acids, or buffers for defoaming during reclaim in the recycling step.
It is still another object of the present invention to have a fracturing fluid to be formulated with a relatively low level of surfactant for cost-effective performance.

DETAILED DESCRIPTION OF THE INVENTION

Surfactants in the self-degrading foaming composition in foamed fracturing fluids promote and stabilize the gas-liquid dispersions are soap-like molecules containing a long hydrophobic paraffin chain with a hydrophilic end group. Such surfactants include anionic and nonionic compounds. Anionic and nonionic surfactants are added in concentrations that range preferably from about 0.05 to about 2 percent of the liquid component volume (from about 0.5 to about 20 gallons per 1000 gallons of liquid); more preferably from about 0.05 to about 1 percent of the liquid component volume.

Anionic Surfactants

Selected anionic surfactants useful in the self-degrading foaming composition of the present invention include dodecylbenzenesulfonates, alpha olefin sulfonates, diphenyloxide disulfonates, alkyl naphthalene sulfonates, sulfosuccinates, sulfosuccinamates, naphthalene-formaldehyde condensates, alkyl sulfoesters and alkyl sulfoamides and mixtures thereof. Preferred anionic surfactants are sulfosuccinates and sulfosuccinamates. Most preferred anionic surfactants are sulfosuccinamates such as disodium lauramide monoethanolamine sulfosuccinamate.
Representative anionic surfactants include those of the following structural formulas:
and combinations thereof.
R₁is selected from a group consisting of alkyl, aryl, alkaryl, alkylarylalkyl, arylalkyl, alkylamidoalkyl and alkylaminoalkyl; wherein the alkyl group has about 10 to about 18 carbon atoms; wherein the aryl group represents a phenyl, diphenyl, diphenylether, or naphthalene moiety.
R₂is selected from a group consisting of hydrogen, —CH₂CH₂OH, alkyl, aryl, alkaryl, alkylarylalkyl, arylalkyl, alkylamidoalkyl and alkylaminoalkyl; wherein the alkyl group has about 10 to about 18 carbon atoms; wherein the aryl group represents a phenyl, diphenyl, diphenylether, or naphthalene moiety.
“p” is 0 to about 10, preferably 0 to about 5.
M is hydrogen, an alkali metal such as sodium or potassium, or an ammonium salt. M is preferably an alkali metal such as sodium or potassium, more preferably sodium.

Nonionic Surfactants

Nonionic surfactants include but not limited to fatty acid esters, glycerol esters, ethoxylated fatty acids esters of glycol, ethoxylated fatty acid esters of polyethylene glycol and sorbitan esters. Preferred nonionic surfactants are glycerol esters, ethoxylated fatty acids esters of glycol and ethoxylated fatty acid esters of polyethylene glycol. Most preferred are ethoxylated fatty acid esters of polyethylene glycol.
Selected nonionic surfactants have the structures:
R₃C(O)O—(CH₂CH₂O)_p—R₄
R₃C(O)OCH₂CH(OH)CH₂O—R₄
and combinations thereof.
R₃is hydrocarbon chain containing about 10 to about 22 carbon atoms and may be branched or straight chained and saturated or unsaturated; R₄hydrogen or a hydrocarbon chain containing about 1 to about 20 carbon atoms and may be branched or straight chained and saturated or unsaturated; “p” is from about 1 to about 20, preferably from about 5 to about 20, more preferably from about 5 to about 12.
The water utilized for forming the foamed fracturing fluid of this invention can be fresh water or salt water. The term “salt water” is used herein to mean unsaturated salt solutions and saturated salt solutions including brines and seawater. In addition water may contain at least one of dissolved organic salts, organic acids, organic acid salts and inorganic salts.
The gelling agent is added to the water for forming the water into gelled water and increasing the viscosity thereof. A variety of gelling agents can be used including natural or derivatized polysaccharides which are soluble, dispersible or swellable in an aqueous liquid to yield viscosity to the aqueous liquid. One group, for example, of polysaccharides which are suitable for use in accordance with the present invention includes galactomannan gums such as gum arabic, gum ghatti, gum karaya, tamarind gum, tragacanth gum, guar gum, locust beam gum and the like. Modified gums such as carboxyalkyl derivatives, like carboxymethylguar and hydroxyalkyl derivatives, like hydroxypropylguar can also be employed. Doubly derivatized gums such as carboxymethylhydroxypropylguar can also be used. Mixtures of the galactomannan gums and modified gums can also be used. Optionally a variety of conventional additives can be included such as gel stabilizers, gel breakers, clay stabilizers, bactericides, fluid loss additives and the like which do not adversely affect the self degrading foaming tendencies of the fracturing fluid.
Foamed fracturing fluids are superior to conventional liquid fracturing fluids for problematic and water sensitive formations because foams contain less liquid than liquid fracturing fluids and have less tendency to leak. Also, foams have less liquid to retrieve after the fracturing operation is complete. Moreover, the sudden expansion of the gas in the foams when pressure in the well is relieved after the fracturing operation is complete promotes flow of residual fracture fluid liquid back into the well. The foamed fracturing fluid can also include a proppant material for preventing formed fractures from closing. A variety of proppant materials can be utilized including, but not limited to, resin coated or un-coated sand, sintered bauxite, ceramic materials and glass beads. When included, the proppant material is preferably present in the foamed fracturing fluid in an amount in the range of from about 1 to about 10 pounds of proppant material per gallon of the foamed fracturing fluid.
Examples of gases suitable for foaming the fracturing fluid of this invention are air, nitrogen, carbon dioxide and mixtures thereof. The gas may be present in the fracturing fluid preferably in an amount in the range of from about 10% to about 95% by volume of liquid, more preferably from about 20% to about 90%, and most preferably from about 20% to about 80% by volume.
The gas volumetric fraction or “foam quality” of useful foamed fracture fluids is preferably in the range of from about 50 volume percent to about 80 volume percent gas. However, stable foams with foam qualities of up to about 95% can be produced. In general, the viscosity of the foamed fluid increases with increasing quality.
The foam quality is expressed as a percentage as shown in the equation below:
[foam volume (ml)−liquid volume (ml)]×[100]/foam volume (ml)
Procedures for making and using foamed fracturing fluids are described in U.S. Pat. No. 3,937,283 to Blauer et al and U.S. Pat. No. 3,980,136 to Plummer et al. Briefly, these patents teach how to produce stable foam fracturing fluids using nitrogen, water, a surfactant and a sand proppant. The foam quality ranges between 53% to 99%. The foam is pumped down the well and into the formation at a pressure sufficient to fracture the formation. When the fracturing operation is complete, the pressure on the well is relieved at the wellhead. The foam is carried back into the well by the rush of expanding gas when pressure on the foam is reduced.
U.S. Pat. No. 3,664,422 to Bullen et al., describe fracturing techniques using carbon dioxide as the gas phase. First, an emulsion of liquefied carbon dioxide and water is formed using a surfactant to promote dispersion. Proppant is added to the emulsion and the emulsion-proppant slurry is pumped down the wellbore into the formation at a pressure sufficient to fracture the subterranean formation. Downhole temperatures are above the critical temperature of carbon dioxide so the liquid carbon dioxide becomes a supercritical fluid as the emulsion approaches the subterranean formation forming a stable foam.
The foamed fracturing fluid in accordance with the present invention may optionally contain water-soluble inorganic salt, e.g. potassium chloride or ammonium chloride and/or at least one organic acid, water-soluble organic acid salt or organic salt, e.g. trimethyl ammonium chloride. These salts are dissolved in water.
In an embodiment of the invention a self-degrading foaming composition is prepared by mixing water with surfactant comprising anionic surfactant, nonionic surfactant, and combinations thereof. The foaming composition may contain an organic solvent. Preferred organic solvent is isopropyl alcohol. Standard mixing procedures known in the art can be employed since heating of the solution and special agitation conditions are normally not necessary. Of course, if used under conditions of extreme cold such as found in Alaska, normal heating procedures should be employed.
In another embodiment of the invention the initial pH of foamed fracturing composition comprising the self-degrading foaming composition may be lowered or raised to decrease the initial foam quality initially and subsequent aging to reduce foam stability. Alternatively it may be possible to raise the pH. The aging is done up to about 24 hours or longer at room temperature. Further, the aging is done at elevated temperatures preferably from about 80° F. to about 180° F. up to about 24 hours or longer.
The aging at 140° F. up to 24 hours or longer is most preferred. The initial decrease of pH may be by brought about by adding acid and/or buffers. It may be possible to add a base and/or buffers to increase the pH of self-degrading foaming composition.
The following examples are presented to illustrate the preparation and properties of foamed fracturing fluids containing self-degrading foaming compositions and should not be construed to limit the scope of the invention, unless otherwise expressly indicated in the appended claims.

EXAMPLES

Foamed fracturing fluids containing self-degrading foaming compositions were prepared and were found to have reduced foam stability after 24 hours of aging. These foams had good quality initially and half-life was substantially reduced after aging at 140° F. for 24 hours.

Materials:

- Gerepon SBL-203 is an anionic surfactant, disodium lauramide monoethanolamine sulfosuccinamate, supplied by Rhodia, Inc.

Alkamuls 600 DO is a nonionic surfactant, PEG-12 dioleate supplied by Rhodia, Inc.

Example 1

A foamed fracturing fluid with a viscosity of 9-10 cP is prepared by diluting a concentrated hydroxypropyl guar solution in tap water. About 100 ml of the fracturing fluid was added to a Waring blender. The surfactant or surfactant blend was then added and the contents of the blender were mixed slowly. As the mixing speed was slowly increased height of the foam increased due to more air being trapped in the foam. The speed was gradually increased until the foam height remains stable and no further increase in the foam height was observed. The blender was shut off, and its contents were immediately poured into a graduated cylinder and a timer was started. The measured volume of the foam in the graduated cylinder was the foam volume and foam quality was determined by the following equation:
Foam quality=100×(foam volume−liquid volume)/foam volume
As time progressed, the foam separated and a clear liquid was collected at the bottom of the cylinder. After 50% of the original liquid was collected in the bottom of the cylinder (i.e. 50 ml) the time was measured. This time was defined as the half-life. After measuring the half-life, the liquid was collected in a bottle and aged in an oven at a set temperature. After a given aging time at the set temperature the bottle was cooled to room temperature and quality and half-life was measured.
The foam volume and time required to reach the half-life (50ml) was measured, exhibiting the recyclable nature of the foamed fracturing. The foam testing results are shown in Table 1.

TABLE 1

Foam Testing Results

			Foam
			Volume		Foam
			(ml) @	Half Life	Quality
Sample ID	Description	Testing Conditions	75 F.	(min:sec)	(%)

	Geropon
	SBL-203 only
R0476-70-5	0.5 ml Geropon	initial	340	31:00	70.6
	SBL-203	24 hrs @ 140 F.	180	9:45	44.4
R0476-70-18	0.2 ml Geropon	initial	305	29:45	67.2
	SBL-203	24 hrs @ 140 F.	185	5:45	48.6
	Geropon SBL-
	203 with
	Alkamuls
	600DO
R0476-70-9	0.2 ml Geropon	initial	275	24:15	63.6
	SBL-203 + 0.05 ml
	Alkamuls 600 DO
		24 hrs @ 140 F.	135	1:30	26.0
R0476-70-10	0.2 ml Geropon	initial	195	7:05	48.7
	SBL-203 + 0.1 ml
	Alkamuls 600 DO
		24 hrs @ 140 F.	125	very	20.0
				fast~5 sec

Example 2

A foamed fracturing fluid of 9-10 cP was prepared as shown in Example 1. The foamed fracturing fluid containing the mixture of surfactants compared with the control Gereopon SBL were studied at various pH values. The foam height, foam quality and half-life were measured at different pH as well as a function of time and are shown in Table 2. The foam quality degraded quickly at higher pH.

TABLE 2

Effect of Initial pH on the Foam Quality and Aging

						Foam			Final
					T	Volume	½		pH
		Solution	Weight	Time	(deg	(ml)	Life	Quality	after
Designation	Surfactant	pH	(g)	(hr)	F.)	@ 75 F.	(min)	(%)	24 hr's

R0476-175-6	Geropon	11.8	100	0	RT	290	34.0	65.5	10.6
	SBL-203		89	2	140	145	3.3	38.6
	(Control)		82	6		130	2.5	36.9
			76	24		120	2.3	36.7
R0476-175-7	R0476-85-11	11.8	100	0	RT	265	19.5	62.3	11.0
			93	2	140	120	0.0	22.5
			—	6
			88	24		125	0.0	29.6
R0476-175-8	R0476-85-11	11.8	100	0	RT	260	16.5	61.5	11.3
			98	2		135	0.5	27.4
			—	6
			91	24		115	0.0	20.9
R0476-175-10	Geropon	10.1	100	0	RT	295	35.0	66.1	9.1
	SBL-203		89	2	140	270	32.0	67.0
	(Control)		82	6		215	23.0	61.9
			75	24		180	17.0	58.3
R0476-175-11	R0476-85-11	10.1	100	0	RT	275	18.0	63.6	9.1
			94	2	140	235	14.0	60.0
			86	6		175	8.0	50.8
			80	24		125	1.5	36.0

R0476-85-11: Formulated by blending 66.67% Geropon SBL-203 + 16.67% Alkamuls 600DO + 8.33% isopropanol + 8.33% Deionized water.

The invention has been described in the more limited aspects of preferred embodiments hereof, including numerous examples. Other embodiments have been suggested and still others may occur to those skilled in the art upon a reading and understanding of the specification. It is intended that all such embodiments be included within the scope of this invention.

Claims

1. A self-degrading foaming composition comprising a mixture of anionic surfactants selected from the group consisting of dodecylbenzenesulfonate, alpha olefin sulfonate, diphenyloxide disulfonate, alkyl naphthalene sulfonate, sulfosuccinate, sulfosuccinamate, naphthalene-formaldehyde condensate, alkyl sulfoester, alkyl sulfoamide, and mixtures thereof; and

a nonionic surfactant selected from the group consisting of fatty acid esters, glycerol esters, ethoxylated fatty acids esters of glycol, ethoxylated fatty acid esters of polyethylene glycol and sorbitan esters;

wherein the self-degrading composition has a substantially reduced foam stability after aging.

2. The composition of claim 1 wherein the anionic surfactant is selected from the group consisting of formula (I), (II), (III), or (IV):

and combinations thereof;

wherein R₁is selected from a group consisting of alkyl, aryl, alkaryl, alkylarylalkyl, arylalkyl, alkylamidoalkyl and alkylaminoalkyl, and

wherein the alkyl group has about 10 to about 18 carbon atoms, the aryl group represents a phenyl, diphenyl, diphenylether, or naphthalene moiety;

R₂is selected from a group consisting of hydrogen, —CH₂CH₂OH, alkyl, aryl, alkaryl, alkylarylalkyl, arylalkyl, alkylamidoalkyl and alkylaminoalkyl, wherein the alkyl group has about 10 to about 18 carbon atoms, wherein the aryl group represents a phenyl, diphenyl, diphenylether, or naphthalene moiety; and

“p” is 0 to about 10, and M represents hydrogen, an alkali metal such as sodium or potassium, or an ammonium salt.

3. The composition of claim 1 wherein said fracturing fluid comprises a crosslinker.

4. The composition of claim 3 wherein said crosslinker is a boron containing compound.

5. The composition of claim 3 wherein said crosslinker is selected from the group consisting of boric acid, borax, boron containing ores, colemanite, and ulexite.

6. The composition of claim 1 wherein said crosslinker is a zirconium or titanium based metallic crosslinker.

7. The composition of claim 1 further comprising cationic surfactants, zwitterionic surfactants, amphoteric surfactants, or mixtures thereof.

8. A foamed fracturing composition comprising:

(a) a self-degrading foaming composition having substantially reduced foam stability after aging, said self-degrading foaming comprising a mixture of anionic surfactants wherein at least one of said anionic surfactants has the general formula:

wherein R₁is selected from a group consisting of alkyl, aryl, alkaryl, alkylarylalkyl, arylalkyl, alkylamidoalkyl and alkylaminoalkyl, and wherein the alkyl group has about 10 to about 18 carbon atoms, the aryl group represents a phenyl, diphenyl, diphenylether, or naphthalene moiety;

R₂is selected from a group consisting of hydrogen, —CH₂CH₂OH, alkyl, aryl, alkaryl, alkylarylalkyl, arylalkyl, alkylamidoalkyl and alkylaminoalkyl, wherein the alkyl group has about 10 to about 18 carbon atoms, wherein the aryl group represents a phenyl, diphenyl, diphenylether, or naphthalene moiety; and at least one nonionic surfactant having the general formula:

R₃C(O)O—(CH₂CH₂O)_pR₄

wherein, R₃is hydrocarbon chain containing about 10 to about 22 carbon atoms, R₄is a hydrogen or a hydrocarbon chain containing about 1 to about 20 carbon atoms; and “p” is from about 1 to about 20

(b) an aqueous solution;

(c) a gelling agent; and

(d) a gas.