US20130146289A1

US20130146289A1 - Two-stage filter cake removal composition for drilling fluids and method of use thereof

Info

Publication number: US20130146289A1
Application number: US13/708,580
Authority: US
Inventors: Abdullah Mohammed Al Moajil; Hisham A. Nasr-El-Din
Original assignee: Saudi Arabian Oil Co
Current assignee: Saudi Arabian Oil Co
Priority date: 2011-12-07
Filing date: 2012-12-07
Publication date: 2013-06-13
Also published as: US10125305B2; US20130146295A1; WO2013086282A1; US20160376491A1

Abstract

Disclosed is a two-stage filter cake removal composition, and method of use thereof, for use in a wellbore for controlled removal of a filter cake present in a target production zone. The two-stage filter cake removal composition may include an enzyme present in an amount of between about 1% and 20%, and a mixture of hydrochloric acid and an organic acid present in amounts of between about 0.1% and 5% and about 0.1% and 10%, respectively, by weight. The two-stage filter cake removal composition, when the enzyme is applied to the filter cake in the target production zone in a first stage and the mixture of the hydrochloric acid and the organic acid is applied to the filter cake in the target production zone in a second stage, is operable to remove the filter cake in the target production zone over an extended reaction time.

Description

RELATED APPLICATION

This application is related to, and claims priority to, U.S. Provisional Patent Application Nos. 61/567,983 and 61/567,993, both provisional applications filed on Dec. 7, 2011, the disclosures of which are incorporated herein by reference in their entirety.

BACKGROUND

1. Field of the Invention
Embodiments of the invention generally relate to methods and compositions for removing a completion fluid filter cake in a wellbore, and more particularly, to methods and compositions for dissolving or removing filter cake material generated by a manganese-tetraoxide-based drilling fluid in a wellbore for optimizing production from a surrounding hydrocarbon bearing formation.
2. Description of the Related Art
Horizontally/multilaterally-drilled wells have been used to enhance both hydrocarbon recovery and total well productivity from many types of reservoirs. Drilling, workover, and production operations may result in near-wellbore formation damage that in most cases cannot be prevented (e.g., pore plugging by calcium carbonate particles from drilling fluid, drilled solid particles, or particles from the formation).
During well operations, drilling fluids can be lost into the surrounding formation. To prevent this, the drilling fluid is frequently modified such that a small amount of the fluid and solids contained therein form a coating on a wellbore surface (i.e., the formation of a “filter cake”). After the completion of drilling operations, the coating or filter cake is typically removed, and production from the formation can proceed. The process used to remove the filter cake can also be used to remove other types of damage or debris from the wellbore prior to beginning hydrocarbon production.
To facilitate the drilling of horizontal/multilateral wells, weighting materials have been introduced into the drilling fluid to increase the density of the drilling fluid for balancing the hydrostatic pressure and for maintaining stability within the wellbore to minimize formation damage and corrosion in the wellbore. Several weighting materials (e.g., bentonite, barite, calcium carbonate (CaCO₃) ilmenite, and hematite) have been used in drilling fluids, each of which has several associated limitations. For example, bentonite and barite are not soluble in hydrochloric acid (HCl), and therefore they may cause formation damage in the wellbore. The specific gravity of CaCO₃(e.g., 2.71) limits its application when a high density drilling fluid is needed to drill deep wells. Due to the partial solubility of barite in concentrated formate brines and the conventional practice not to acidize the wellbore prior to completion of the well, CaCO₃and barite have been excluded as options to increase density of the drilling fluid in many applications.
Manganese tetraoxide (Mn₃O₄) is a high density, acid-soluble weighting material useful in drilling fluids for drilling high temperature/high pressure (HT/HP) wells. Mn₃O₄is spherical in shape and has an average partial size of 1-5 microns and a specific gravity of 4.8, which make it appropriate for drilling deep wells. For example, Mn₃O₄has been introduced into potassium formate drilling fluids to overcome the main drawback of potassium formate, which is the production of a brine of density 1.7 g/cm3 (106 lb/ft3). Mn₃O₄has also been introduced as a weighting material into oil-based drilling fluids due to its ability to lower the plastic viscosity of the oil-based drilling fluid. A water-based drilling fluid weighted with Mn₃O₄and a small amount of CaCO₃has also been formulated for use in a wellbore. CaCO₃has been added to the water-based drilling fluid to control filtration properties of the drilling fluid. The need in the industry for a drilling fluid with high rheological properties has been achieved using Mn₃O₄particles.
Mn₃O₄particles, however, also present many disadvantages as a weighting material in oil-based or water-based drilling fluids. For example, Mn₃O₄particles aggregate up to 20 microns in aqueous and oil-based fluids. Accumulation of these aggregates in the critical near wellbore area can result in stuck pipe and mud cake problems during drilling operations. Dust problems associated with the accumulation of these aggregates have also caused formation damage in the wellbore. Additionally, starch may be present in the filter cake covered Mn₃O₄particles, which can contribute to additional particle agglomeration. Thus, addressing the removal of a filter cake formed by a drilling fluid weighted with Mn₃O₄particles is essential to ensure the effectiveness of drilling and cleaning operations in the wellbore.
Several cleaning compositions have been developed to remove the filter cake generated by a manganese-tetraoxide-based drilling fluid from the wellbore and to minimize formation damage in the wellbore using live acids, gelled acids, strongly buffered organic acids, chelating agents, oxidizing agents, enzymes, in-situ generated organic acids, microemulsions, or combinations of these chemicals. Because Mn₃O₄is a strong oxidizing agent having an active phase (i.e., a tetragonal symmetry, non-stoichiometry behavior) locally composed of an octahedral Mn2O3 phase and a tetrahedral MnO phase, it experiences complex interactions with most cleaning fluids, including the aforementioned chemicals. For example, organic acids and chelating agents will not independently dissolve Mn₃O₄-based filter cakes. Ethylene diamine tetracetic acid (EDTA) at high pH (e.g., a pH of 12) and acetic, propionic, butyric, and gluconic acids at low pH (e.g., a pH of 3-5) exhibit very low solubility. Glutamic, citric, oxalic, and tartaric acids produce white precipitation when reacted with Mn₃O₄particles. Similarly, diethylene triaminen pentaacetic acid (DTPA) precipitates manganese silicate if used to dissolve Mn₃O₄-based filter cake in a sandstone formation.
Citric acid in an amount of about 10% by weight has been used as a cleaning fluid for effectively removing Mn₃O₄,-based filter cakes. However, when reacted with Mn₃O₄, citric acid has been known to dissociate insoluble manganese citrate causing formation damage in the wellbore, and therefore is not a suitable composition to effectively dissolve or remove the Mn₃O₄-based filter cake from the wellbore while preventing formation damage.
Therefore, what is needed is a filter cake removal composition which dissolves, and more preferably removes, a filter cake generated by a manganese-tetraoxide-based drilling fluid without causing formation damage in the wellbore.

SUMMARY

Embodiments of the invention are directed to compositions, and methods of use thereof, for dissolving or removing filter cake material generated by a manganese-tetraoxide-based drilling fluid in a wellbore for optimizing production from a surrounding hydrocarbon bearing formation. An embodiment of the invention includes a filter cake removal composition including HCl having a concentration lower than 5% by weight for partially dissolving the Mn₃O₄-based filter cake. According to another embodiment of the invention, a two-stage filter cake removal composition is provided which includes an enzyme that is first applied to the filter cake, followed by the application of an organic acid to the resulting filter cake. In accordance with another embodiment of the invention, there is provided a single-stage filter cake removal composition including a mixture of HCl and an organic acid for dissolving a portion of the filter cake in the wellbore, which will be described in more detail below. According to another embodiment of the invention, there is provided a two-stage filter cake removal composition that has been demonstrated to remove filter cake material generated by a manganese-tetraoxide-based drilling fluid in a wellbore using the application of an amylase enzyme in a first stage, followed by the application of a mixture of HCl and an organic acid in a second stage, which will also be described in further detail below. Methods of use of the latter two filter cake removal compositions will also be described in further detail below.
In particular, there is provided a two-stage filter cake removal composition, in accordance with an embodiment of the invention, for use in a wellbore for controlled removal of a filter cake present in a target production zone. The two-stage filter cake removal composition includes an enzyme present in an amount of between about 1% and 20%, and a mixture of hydrochloric acid and an organic acid present in amounts of between about 0.1% and 5% and about 0.1% and 10%, respectively, by weight. The two-stage filter cake removal composition, when the enzyme is applied to the filter cake in the target production zone in a first stage and the mixture of the hydrochloric acid and the organic acid is applied to the filter cake in the target production zone in a second stage, is operable to remove the filter cake in the target production zone over an extended reaction time.
In accordance with another embodiment of the invention, there is provided a method for the controlled removal of a filter cake from a target production zone of a wellbore using a two-stage filter cake removal composition. The method includes delivering the two-stage filter cake removal composition to the target production zone. The two-stage filter cake removal composition contacts the filter cake for an extended reaction time during which extended time the two-stage filter cake removal composition acts to remove the filter cake and after which extended time the two-stage filter cake removal composition acts to control fluid loss from the wellbore into the target production zone. The step of delivering includes applying an enzyme of the two-stage filter cake removal composition to the filter cake in the target production zone in a first stage and applying a mixture of hydrochloric acid and an organic acid of the two-stage filter cake removal composition to the filter cake in the target production zone in a second stage.

BRIEF DESCRIPTION OF DRAWINGS

So that the manner in which the features and advantages of the invention, as well as others which will become apparent, may be understood in more detail, a more particular description of the invention briefly summarized above may be had by reference to the embodiments thereof which are illustrated in the appended drawings, which form a part of this specification. It is to be noted, however, that the drawings illustrate only various embodiments of the invention and are therefore not to be considered limiting of the invention's scope as it may include other effective embodiments as well.

FIG. 1 shows a filter cake before and after an application of a filter cake removal composition, including 10% by weight of HCl, in accordance with an embodiment of the invention.

FIG. 2 shows a gas chromatography/mass spectrometry graph illustrating the relationship between the reaction of HCl with Mn₃O₄particles and the production of chlorine gas, in accordance with an embodiment of the invention.

FIG. 3 is a graph showing the effect of Mn₃O₄-high soluble organic acids on the dissolution of manganese ions, in accordance with an embodiment of the invention.

FIG. 4 shows a filter cake before and after an application of a two-stage filter cake removal composition, in accordance with an embodiment of the invention

FIG. 5 shows a graph illustrating the efficacy of a mixture of HCl and lactic acid for the dissolution of manganese ions from a Mn₃O₄-based filter cake, in accordance with an embodiment of the invention.

FIG. 6 shows a graph illustrating the solubility of a Mn₃O₄-based filter cake and acid concentration as a function of time using a two-stage filter cake removal composition, in accordance with an embodiment of the invention.

FIG. 7 shows the efficacy of a single-stage filter cake removal composition, in accordance with an embodiment of the invention, for removing Mn₃O₄particles from a filter cake.

DETAILED DESCRIPTION

Although the following detailed description contains many specific details for purposes of illustration, it is understood that one of ordinary skill in the relevant art will appreciate that many examples, variations, and alterations to the following details are within the scope and spirit of the invention. Accordingly, the exemplary embodiments of the invention described herein are set forth without any loss of generality, and without imposing limitations, relating to the claimed invention. Like numbers refer to like elements throughout. Prime notation, if used, indicates similar elements in alternative embodiments.
As used herein, the term “drilling fluid” shall be used to collectively refer to a completion fluid or a drilling fluid. As understood in the art, “drilling fluid” shall be used to describe a fluid used to aid in the drilling of a borehole for a well (e.g., a horizontal/multilateral well). The drilling fluid may include a water-based mud (e.g., a dispersed or non-dispersed water-based mud), a non-aqueous mud (e.g., an oil-based mud), and a gaseous drilling fluid.
Experimentation of conventional cleaning fluids demonstrates that Mn₃O₄deposits dissolve in concentrated (e.g., ˜12N) or dilute (e.g., ˜3N) HCl solutions. The reaction of HCl with Mn₃O₄depends on the stoichiometry of the reactants as shown, for example, in Equations (1)-(3):
Mn₃O₄+8HCl
2MnCl₂+MnCl₄+4H₂O (1)
3Mn₃O₄+12HCl
6MnCl₂+MnO₂+6H₂O (2)
Mn₃O₄+6HCl
MnCl₂+MnCl₄+3H₂O (3)
Embodiments of the invention demonstrate that HCl in an amount of about 10% by weight may dissolve about 78% by weight of a Mn₃O₄-based filter cake at about 250° F. after 28 hours of soaking the filter cake material. However, corrosive/poisonous chlorine gas is detected during the reaction of between about 5 and 15% by weight of HCl with Mn₃O₄, as given, for example, by Equation (4):
Mn₃O₄+8HCl
3MnCl₂+Cl₂+4H₂O (4)
Certain embodiments of the invention demonstrate that, at about 190° F., an amount of between about 1 and 4% by weight HCl may dissolve most of the Mn₃O₄particles in the filter cake (e.g., up to about 70% by weight solubility), without the release of chlorine gas. The reaction of HCl in an amount of between about 1 and 4% by weight and Mn₃O₄particles at about 190° F. may be represented by equation (5):
Mn₃O₄+4HCl
2MnCl₂+MnO₂+2H₂O (5)
Therefore, HCl at a concentration of less than about 5% by weight will partially dissolve a Mn₃O₄-based filter cake.
Embodiments of the invention further demonstrate that about 4% by weight of an organic acid, such as lactic or formic acid, as non-limiting examples, may dissolve Mn₃O₄particles up to about 76% by weight solubility at about 190° F. However, it has been observed that the Mn₃O₄particles of the filter cake were covered with polymeric material (e.g., starch), which significantly reduces the solubility of the filter cake in the organic acids. Therefore, there is a need to remove the polymeric material on the Mn₃O₄particles of the filter cake to more effectively dissolve or remove the filter cake material in the wellbore. Certain embodiments of the invention provide for the application of an enzyme (i.e., an enzyme that catalyzes the breakdown of starch into sugars) to remove the polymeric material present on the Mn₃O₄particles of the filter cake.
Certain embodiments of the invention provide for a filter cake removal composition, and method of use thereof, for use in a wellbore for the controlled removal of a filter cake present in a target production zone. Generally, the filter cake removal composition includes low and safe concentrations of HCl combined with an organic acid. The filter cake removal composition, when a mixture of the HCl and the organic acid is delivered or applied to the filter cake in the target production zone, may be operable to dissolve the filter cake in the target production zone over an extended reaction time, and subsequently may be operable to control fluid loss from the wellbore into the target production zone. For example, the filter cake removal composition can be delivered or applied to the filter cake in a single-stage treatment, whereby the filter cake is allowed to soak in the cleaning fluid for up to about 24 hours. According to an embodiment of the invention, the hydrochloric acid is present in an amount of between about 0.1% and 5% by weight and the organic acid in an amount of between about 0.1% and 10% by weight.
In accordance with another embodiment of the invention, the hydrochloric acid is preferably present in an amount of about 1% by weight. The organic acid may be selected from the group consisting of formic acid, lactic acid, and malonic acid. In accordance with another embodiment of the invention, the organic acid includes lactic acid and is preferably present in an amount of about 4% by weight.
According to an embodiment of the invention, about 1% by weight HCl combined with about 4% by weight lactic acid may dissolve, in a single stage treatment of the filter cake, about 85% by weight of the Mn₃O₄-based filter cake after about 18-22 hours of soaking at a temperature of about 250° F.
Other embodiments of the invention provide a two-stage filter cake removal composition, and method of use thereof, for use in the wellbore for controlled removal of the filter cake present in the target production zone. Generally, the two-stage filter cake removal composition includes an enzyme and a mixture of HCl and an organic acid. The two-stage filter cake removal composition, when the enzyme is delivered or applied to the filter cake in the target production zone in a first stage and the mixture of the hydrochloric acid and the organic acid is applied to the filter cake in the target production zone in a second stage, is operable to remove the filter cake in the target production zone over an extended reaction time. Subsequently, the delivery or application of the two-stage filter cake removal composition is operable to control fluid loss from the wellbore into the target production zone.
In accordance with an embodiment of the invention, the enzyme includes an enzyme that catalyzes the breakdown of starch into sugars to remove the polymeric material present on the Mn₃O₄particles of the filter cake for more effectively dissolving or removing the filter cake material in the wellbore. According to an embodiment of the invention, the enzyme includes an amylase enzyme present in an amount of between about 1% and 20% by weight. The amylase enzyme may include, for example, an α-amylase enzyme, a β-amylase enzyme, or a γ-amylase enzyme. In a preferred embodiment, the enzyme of the two-stage filter cake removal composition is an α-amylase enzyme present in an amount of about 10% by weight.
In accordance with another embodiment of the invention, the hydrochloric acid is present in an amount of between about 0.1% and 5% by weight, and more preferably in an amount of between about 1 and 2% by weight.
In accordance with another embodiment of the invention, the organic acid includes a carboxylic acid present in an amount of between about 0.1% and 10% by weight, and more preferably the organic acid is a carboxylic acid selected from the group consisting of formic acid, lactic acid, and malonic acid. In one embodiment, the organic acid includes one of formic acid and lactic acid present in an amount of about 4% by weight.
In accordance with certain embodiments of the invention, the enzyme is applied to the filter cake in the target production zone for a predetermined period of time based on one of a characteristic of the filter cake, an enzyme type, concentration of the enzyme, and the thermal stability of the enzyme. For example, the enzyme may be applied to the filter cake for a predetermined period of time of up to about 24 hours, and more preferably for about 16-24 hours.
In accordance with certain embodiments of the invention, the concentrations of the enzyme, the HCl, and the organic acid are based on one or more factors, including, but not limited to, the reservoir temperature, formation mineralogy and composition, filter cake characteristics and composition, enzyme activity, and thermal stability.

EXAMPLES

The examples described below show certain exemplary embodiments of the filter cake removal composition of the present invention, as described herein. As shown in Table 1, water-based drilling fluids primarily weighted with Mn₃O₄and a small amount of CaCO₃particles to control a leak-off rate were prepared to demonstrate the efficacy of the filter cake removal composition, in accordance with certain embodiments of the invention, for dissolving or removing filter cake material in a wellbore. Xanthan, starch, and polyanionic cellulose (PAC-R) polymers were added to the mud to control fluid loss and rheological properties of the drilling fluid. Lime (Ca(OH)₂) and potassium hydroxide (KOH) were added to adjust the pH of the drilling fluid. Sodium sulfite (Na₂SO₃) was added to the drilling fluid as an oxygen scavenger.

TABLE 1

TABLE 1 - FORMULATION OF DRILL-IN FLUID

Amount added

	Lab units	Field unit
	(per ~320 cm³)	(per bbl)

Additive	Function	Quantity	Unit	Quantity	Unit

DI Water	Base	287.7	cm³	0.822	bbl
Xanthan	Viscosifier	1	G	1	lb
Starch	Fluid loss control	6	G	6	lb
	agent
PAC-R	Viscosifier/fluid loss	0.75	G	0.75	lb
KCl	Density and shale	41	G	41	lb
	inhibition
KOH	pH control	0.5	G	0.5	lb
Ca(OH)₂	pH control	0.25	G	0.25	lb
CaCO₃	Weighting material	3.5	G	3.5	lb
(Fine)
CaCO₃	Weighting material	1.5	G	1.5	lb
(Medium)
Mn₃O₄	Weighting material	202	G	202	lb
Na₂SO₃	Oxygen scavenger	0.75	G	0.75	lb

Table 2 summarizes the main properties of the prepared manganese-tetraoxide-based drilling fluid shown above in Table 1.

TABLE 2

TABLE 2 - PROPERTIES OF Mn₃O₄DRILL-IN FLUID

Property	Conditions	Unit	Value

Density	80° F. and 14.7 psi	lb/ft³	95
Plastic	120° F. and 14.7 psi	cp	27
viscosity
Yield point		lb/100 ft²	38
API filtrate	Static at 75° F. and 100 psi	cm³/30 min	6.5
Cake		In	1/32
thickness
HPHT	Dynamic at 250° F. and 200 psi	cm³/30 min	13.6-20.3
filtrate	3 μm, 400 md ceramic disc
Cake		In	0.24-0.29
thickness
pH	—	—	10-11

According to various embodiments of the invention, HCl is effective for dissolving Mn₃O₄particles and the Mn₃O₄-based filter cake. For example, as shown in FIG. 1, HCl in an amount of about 10% by weight may dissolve about 78% by weight of a Mn₃O₄-based filter cake at about 250° F. and about 250 psi after about 28 hours of soaking time (i.e., a filter cake thickness of about 0.171 in. prior to delivery or application of the filter cake removal composition; a filter cake thickness of about 0.03 in. after delivery or application of the filter cake removal composition). However, as discussed above, chlorine gas is detected during the reaction of between about 5 to 15% by weight HCl with Mn₃O₄particles. FIG. 2 shows a gas chromatography/mass spectrometry graph illustrating chlorine gas produced during the reaction of between about 5 to 15% by weight HCl with Mn₃O₄particles at about 284° F. As shown in FIG. 2, HCl should not be used at concentrations higher than 5% by weight in order to prevent the production of chlorine gas. At HCl concentrations lower than 5% by weight, however, the filter cake removal efficiency by weight is only about 50% by weight, and therefore is not much more efficient than conventional cleaning fluids.
Table 3 shows the solubility of Mn₃O₄particles in HCl at 1%, 4%, and 10% by weight HCl at about 190° F. Table 3 shows that a concentration of HCl of about 4% by weight is effective, however, at dissolving a portion of the Mn₃O₄-solid particles in the filter cake (e.g., about 70% by weight) without producing chlorine gas, even though as shown in FIG. 2, this concentration of HCl does not allow for a filter cake removal efficiency that is much greater than conventional cleaning fluids.

TABLE 3

TABLE 3 - SOLUBILITY OF Mn₃O₄PARTICLES
IN HCl ACID SOLUTIONS, 190° F.

		Weight of retained	Manganese
HCl Concentration,	Dissolved	solids after reaction,	Concentration,
wt %	solids, wt %	g	mg/l

1	56	1.76	~7,500
4	70	1.2	~8,500
10	100	0	~18,000

Embodiments of the invention further demonstrate that organic acids may be used to dissolve or remove Mn₃O₄particles from the filter cake. As shown in Table 4, at about 4% by weight acid concentration, organic acids, such as lactic and formic acids, as non-limiting examples, may dissolve Mn₃O₄particles up to 76% by weight solubility at about 190° F. Malonic acid may be used to dissolve Mn₃O₄particles in the filter cake, but it may not be as effective as formic and lactic acids (i.e., only about 50% by weight of the Mn₃O₄-solid particles in the filter cake are dissolved).

TABLE 4

TABLE 4 - SOLUBILITY OF Mn₃O₄PARTICLES (4 g)
IN ORGANIC ACIDS SOLUTIONS (200 g), 190° F.

Acid type	Dissolved	Manganese
(concentration,	solids,	Concentration,	%
wt %)	wt %	mg/l	of Consumed acid

4 wt % lactic acid +	99	14,600 at 10 min	66.5
1 wt % HCl
Formic (4)	76.4	11,000 at 70 min	52.6
Lactic acid (4)	70.2	8,900 at 35 min	75.9
Malonic (2)	53.73	6,600 at 25 min	60

In a preferred embodiment of the invention, a mixture of HCl, for example, in an amount of about 0.1% and about 5% by weight, and the organic acid, for example, in an amount of about 0.1% and about 10% by weight, is delivered or applied to the filter cake in a target production zone of a wellbore. As shown in Table 4, for example, a mixture of 1% by weight HCl and 4% by weight lactic acid may dissolve about 99% by weight of the Mn₃O₄-solid particles in the filter cake. As previously discussed, this mixture of HCl and lactic acid may be operable to dissolve about 85% by weight of the filter cake.
Certain embodiments of the invention provide a two-stage filter cake removal composition for controlled removal of a filter cake present in a target production zone. As previously discussed above, Mn₃O₄particles in the filter cake may be covered with polymeric material (e.g., starch), which significantly reduces the solubility of the filter cake in organic acids. In order to remove the polymeric material, embodiments of the invention provide a two-stage filter cake removal composition which includes the application of an enzyme in a first stage and the application of a mixture of HCl and an organic acid in a second stage.
Experimentation demonstrates that an amylase enzyme in an amount of about 10% by weight and an in-situ lactic acid in an amount of about 10% by weight may dissolve about 84% by weight of the filter cake at about 244° F. after soaking the filter cake in the organic acid for about 24 hours (see FIG. 4). The enzyme soaking stage time is about 4 days. Dissolving the filter cake created by Mn₃O₄water-based drilling fluids using a two-stage treatment may increase the time of the treatment (e.g., 1-4 days for the enzyme stage alone) depending on various factors, for example, filter cake polymeric composition, enzyme type, concentration and thermal stability, as non-limiting examples. Adding HCl to the second stage of the treatment reduces the required enzyme and organic acid concentrations and the soaking time to about 24 hours for each stage.
For example, the two-stage filter cake removal composition, in accordance with certain embodiments of the invention, provides complete solubility of the Mn₃O₄particles (e.g., about 99% by weight) in the filter cake, when a mixture of low and safe concentrations of HCl, for example, in an amount of about 1% by weight, and an organic acid, for example, of about 4% by weight of lactic acid, is applied to a filter cake after the filter cake is treated with an initial stage of an enzyme, for example, an amylase enzyme in an amount of about 10% by weight, which dissolves about 85% by weight of the Mn₃O₄-based filter cake after about 18 hours soaking time at about 250° F.
FIG. 5 shows a graph illustrating that a mixture of HCl and lactic acid may be more effective in the dissolution of manganese ions from the Mn₃O₄-based filter cake than with a treatment of only lactic acid or only HCl, in accordance with an embodiment of the invention. FIG. 6 shows a graph illustrating the solubility of the Mn₃O₄-based filter cake and acid concentration as a function of time using the mixture of about 1% by weight HCl and about 4% by weight lactic acid at about 250° F. and about 250 psi. FIG. 7 shows a filter cake thickness of about 0.174 in. prior to delivery or application of the single-stage filter cake removal composition, in accordance with an embodiment of the invention, and a filter cake thickness of about 0.026 in and about 0.024 in. after soaking the Mn₃O₄-based filter cake in the two-stage filter cake removal composition for about 18 hours and about 22 hours, respectively. No enzyme was used in the filter cake removal composition represented by FIGS. 6 and 7.
Embodiments of the present invention may suitably comprise, consist or consist essentially of the elements disclosed and may be practiced in the absence of an element not disclosed. For example, it can be recognized by those skilled in the art that certain steps can be combined into a single step.
Unless defined otherwise, all technical and scientific terms used have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
The singular forms “a,” “an,” and “the” include plural referents, unless the context clearly dictates otherwise.
As used herein and in the appended claims, the words “comprise,” “has,” and “include” and all grammatical variations thereof are each intended to have an open, non-limiting meaning that does not exclude additional elements or steps.
Ranges may be expressed herein as from about one particular value, and/or to about another particular value. When such a range is expressed, it is to be understood that another embodiment is from the one particular value and/or to the other particular value, along with all combinations within said range.
Although the present invention has been described in detail, it should be understood that various changes, substitutions, and alterations can be made hereupon without departing from the principle and scope of the invention. Accordingly, the scope of the present invention should be determined by the following claims and their appropriate legal equivalents.

Claims

What is claimed is:

1. A two-stage filter cake removal composition for use in a wellbore for controlled removal of a filter cake present in a target production zone, the two-stage filter cake removal composition comprising:

an enzyme; and

a mixture of hydrochloric acid and an organic acid,

wherein the two-stage filter cake removal composition, when the enzyme is applied to the filter cake in the target production zone in a first stage and the mixture of the hydrochloric acid and the organic acid is applied to the filter cake in the target production zone in a second stage, is operable to remove the filter cake in the target production zone over an extended reaction time.

2. The two-stage filter cake removal composition of claim 1, wherein the enzyme is selected from the group consisting of an α-amylase enzyme, a β-amylase enzyme, and a γ-amylase enzyme, the enzyme being present in an amount of between about 1 to about 20% by weight.

3. The two-stage filter cake removal composition of claim 2, wherein the enzyme comprises the α-amylase enzyme present in an amount of about 10% by weight.

4. The two-stage filter cake removal composition of claim 1, wherein the hydrochloric acid is present in an amount of between about 0.1% and 5% by weight.

5. The two-stage filter cake removal composition of claim 1, wherein the organic acid comprises a carboxylic acid present in an amount of between about 0.1% and 10% by weight.

6. The two-stage filter cake removal composition of claim 1, wherein the organic acid is selected from the group consisting of formic acid, lactic acid, and malonic acid.

7. The two-stage filter cake removal composition of claim 1, wherein the organic acid comprises one of formic acid and lactic acid present in an amount of about 4% by weight.

8. The two-stage filter cake removal composition of claim 1, wherein the filter cake removal composition comprises the mixture of the hydrochloric acid present in an amount of between about 1% and 2% by weight and the organic acid present in an amount of about 4% by weight.

9. The two-stage filter cake removal composition of claim 1, wherein the enzyme is applied to the filter cake in the target production zone in the first stage for a predetermined period of time based on one of a characteristic of the filter cake, an enzyme type, a concentration of the enzyme, and a thermal stability of the enzyme.

10. The two-stage filter cake removal composition of claim 1, wherein the enzyme is applied to the filter cake in the target production zone in the first stage for about 1 to 4 days, and the mixture of the hydrochloric acid and the organic acid is applied to the filter cake in the target production zone in the second stage for about 18 hours at about 250° F.

11. A method for the controlled removal of a filter cake from a target production zone of a wellbore using a two-stage filter cake removal composition, the method comprising:

delivering the two-stage filter cake removal composition to the target production zone,

wherein the two-stage filter cake removal composition contacts the filter cake for an extended reaction time during which extended time the two-stage filter cake removal composition acts to remove the filter cake and after which extended time the two-stage filter cake removal composition acts to control fluid loss from the wellbore into the target production zone, and

wherein the delivering comprises applying an enzyme of the two-stage filter cake removal composition to the filter cake in the target production zone in a first stage and applying a mixture of hydrochloric acid and an organic acid of the two-stage filter cake removal composition to the filter cake in the target production zone in a second stage.

12. The method of claim 11, wherein the enzyme is selected from the group consisting of an α-amylase enzyme, a β-amylase enzyme, and a γ-amylase enzyme, the enzyme being present in an amount of between about 1 to about 20% by weight.

13. The method of claim 12, wherein the delivering further comprises applying the α-amylase enzyme present in the amount of about 10% by weight to the filter cake in the target production zone for about 1-4 days.

14. The method of claim 11, wherein the delivering further comprises applying the enzyme present in an amount of between about 1% and 20% by weight to the filter cake in the target production zone for a predetermined period of time based on one of a characteristic of the filter cake, an enzyme type, a concentration of the enzyme, and a thermal stability of the enzyme.

15. The method of claim 11, wherein the delivering further comprises applying the mixture of the hydrochloric acid present in an amount of between about 0.1% and 5% by weight and the organic acid present in an amount of between about 0.1% and 10% by weight.

16. The method of claim 15, wherein the organic acid comprises one of formic acid and lactic acid present in an amount of about 4% by weight.

17. The method of claim 11, wherein the delivering further comprises applying the mixture of the hydrochloric acid present in the amount of about 1% to 2% by weight and the organic acid present in the amount of about 4% by weight.

18. The method of claim 11, wherein the applying the enzyme comprises applying the enzyme of the two-stage filter cake removal composition to the filter cake in the target production zone for a first predetermined period of time based on one of a characteristic of the filter cake, an enzyme type, a concentration of the enzyme, and a thermal stability of the enzyme, wherein the enzyme concentration of the two-stage filter cake removal composition is between about 1% and 20% by weight, and

wherein the applying the mixture comprises soaking, after applying the enzyme, the filter cake in the target production zone with the mixture of the hydrochloric acid and the organic acid for a second predetermined period of time, wherein the concentrations of the hydrochloric acid and the organic acid are between about 0.1% and 5% and about 0.1% and 10%, respectively, by weight.

19. The method of claim 18, wherein the concentration of the enzyme is about 10%, the concentration of the hydrochloric acid is about 2%, and the concentration of the organic acid is 4% by weight, for the filter cake removal composition.

20. The method of claim 18, wherein the first predetermined period of time is about 1-4 days and the second predetermined period of time is about 16-24 hours.