Composition and Method for Improving the Production of Petroleum Hydrocarbons
20230069858 · 2023-03-09
Assignee
Inventors
- Jiangshui Huang (Sugar Land, TX)
- Nancy ZHOU (Sugar Land, TX, US)
- Lijun Lin (Katy, TX, US)
- Fuchen Liu (Panjin, CN)
- Guodong WU (Beijing, CN)
- Bo Huang (Beijing, CN)
Cpc classification
C09K8/90
CHEMISTRY; METALLURGY
E21B37/06
FIXED CONSTRUCTIONS
C09K8/584
CHEMISTRY; METALLURGY
E21B41/02
FIXED CONSTRUCTIONS
International classification
C09K8/66
CHEMISTRY; METALLURGY
C09K8/60
CHEMISTRY; METALLURGY
Abstract
A novel surfactant composition that comprises of two surfactant components, a solvent, and water. The surfactant composition is added to a fracturing fluid, which is then pumped downhole into a subterranean formation where the novel characteristics of the fracturing fluid lend to improved oil production over the fracturing fluid without the surfactant composition.
Claims
1. A method of increasing the production of petroleum hydrocarbons comprising: formulating a surfactant solution; mixing the surfactant solution with a fracturing fluid to form a fracturing fluid composition; injecting the fracturing fluid composition into a well bore at a flow rate and pressure sufficient to fracture the subterranean formation; wherein the surfactant solution comprises a first surfactant, a second surfactant, a solvent, and water; and wherein the production of petroleum hydrocarbons from the well bore is increased in comparison to production of petroleum hydrocarbons if the surfactant solution was not added to the fracturing fluid composition.
2. The method of claim 1 wherein the surfactant solution is mixed with the fracturing fluid to a concentration of 0.02 to 50 gallon per thousand gallons of the fracturing fluid.
3. The method of claim 1: wherein the first surfactant is an ether sulfonate having the formula: R.sub.1O(R.sub.2O).sub.x(R.sub.3O).sub.yCH.sub.2CH(OH)CH.sub.2SO.sub.3M, wherein R.sub.1 is a linear or branched alkyl group having 5 to 30 carbon atoms, R.sub.2 is —CH.sub.2CH.sub.2—, R.sub.3 is —CH(CH.sub.3)CH.sub.2—, x is an integer from 2 to 30, y is an integer from 0 to 20, and M is a monovalent cation; wherein the second surfactant is an alkyl alkoxylated nonionic surfactant having the formula R.sub.4)O(R.sub.2O).sub.m(R.sub.3O).sub.nH, where R.sub.4 is a linear or branched alkyl group having 5 to 30 carbon atoms, m is an integer from 5 to 30, and n is an integer from 1 to 20; and wherein the solvent is methanol, ethanol, isopropanol, 1-propanol, butanol, acetone, ethyl lactate, glycerol, ethylene glycol, ethylene glycol butyl ether, butyl acetate, acetic acid, or any combination thereof.
4. The method of claim 3 wherein the fracturing fluid composition further comprises a gelling agent, a proppant, a biocide, a scale inhibitor, a clay stabilizer, a friction reducer, a crosslinking agent, a breaker, a thermal stabilizer, a pH adjuster, a corrosion inhibitor, an iron control agent, or any combination thereof.
5. The method of claim 4 wherein the gelling agent is selected from the group comprising: hydroxyethyl guar, carboxymethyl guar, hydroxypropyl guar, carboxymethylhydroxypropyl guar, carboxymethylhydroxyethyl guar, carboxyethylcellulose,hydroxyethyl cellulose, carboxymethylhydroxyethylcellulose, carboxymethylcellulose, xanthan, diutan, or any combination thereof.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0011] In order that the manner in which the above-recited and other enhancements and objects of the disclosure are obtained, a more particular description of the disclosure briefly described above will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. Understanding that these drawings depict only typical embodiments of the disclosure and are therefore not to be considered limiting of its scope, the disclosure will be described with additional specificity and detail through the use of the accompanying drawings in which:
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DETAILED DESCRIPTION
[0020] The particulars shown herein are by way of example and for purposes of illustrative discussion of the preferred embodiments of the present disclosure only and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of various embodiments of the disclosure. In this regard, no attempt is made to show structural details of the disclosure in more detail than is necessary for the fundamental understanding of the disclosure, the description taken with the drawings making apparent to those skilled in the art how the several forms of the disclosure may be embodied in practice.
[0021] The following definitions and explanations are meant and intended to be controlling in any future construction unless clearly and unambiguously modified in the following examples or when application of the meaning renders any construction meaningless or essentially meaningless. In cases where the construction of the term would render it meaningless or essentially meaningless, the definition should be taken from Webster’s Dictionary 3.sup. rd Edition.
Anionic Surfactants, Nonionic Surfactants, and Solvents
Anionic Surfactants #1-3
[0022] The ether sulfonate (anionic surfactants) tested herein have the following formula: [0023] R.sub.1O(R.sub.2O).sub.x(R.sub.3O).sub.yCH.sub.2CH(OH)CH.sub.2SO.sub.3M. [0024] Where R.sub.1 is C.sub.11 to C.sub.14 iso-alkyl, R.sub.2 is ethyl, and R.sub.3 is propyl with structure of CH(CH.sub.3)CH.sub.2. [0025] Anionic surfactant #1: x=9 and y=4; [0026] Anionic surfactant #2: x=9 and y=12; [0027] Anionic surfactant #3: x=18 and y=0.
Nonionic Surfactants #1-3
[0028] The alkyl alkoxylated nonionic surfactants tested herein have the following formula: [0029] R.sub.4O(R.sub.2O).sub.m(R.sub.3O).sub.nH [0030] Where R4 is C.sub.11 to C.sub.14 iso-alkyl. R.sub.2 is ethyl, R.sub.3 is propyl with structure of CH(CH.sub.3)CH.sub.2. [0031] Nonionic #1: m=18 and n=1; [0032] Nonionic #2: m=9 and n=4; [0033] Nonionic #3: m=9 and n=12.
Solvents
[0034] In an embodiment, the solvent is at least one or any combination of the solvents including, but not limited to, methanol, ethanol, isopropanol, 1-propanol, butanol, acetone, ethyl lactate, glycerol, ethylene glycol, ethylene glycol butyl ether, butyl acetate, and acetic acid. In an embodiment, the solvent is one or any combination of solvents known to one of ordinary skill in the art for use in a wellbore.
[0035] In an embodiment, ethylene glycol butyl ether can be used as a solvent in the surfactant solution. Ethylene glycol butyl ether (Solvent #1) tested herein has the following structure: [0036] CH.sub.3CH.sub.2CH.sub.2CH.sub.2OCH.sub.2CH.sub.2OH
Surfactant Solutions
[0037] In an embodiment, various surfactant solutions were made by combining an anionic surfactant, a nonionic surfactant, a solvent, and water.
TABLE-US-00001 Surfactant Solutions #1-3 Surfactant solution #1 Surfactant solution #2 Surfactant solution #3 Anionic #1: 13.0 wt. % Anionic #2: 13.0 wt. % Anionic #3: 14.8 wt. % Nonionic #1: 43.0 wt. % Nonionic #2: 35.2 wt. % Nonionic #3: 34.2 wt. % Solvent #1: 11.4 wt. % Solvent #1: 9.3 wt. % Solvent #1: 9.2 wt. % Water: 32.6 wt. % Water: 42.5 wt. % Water: 41.8 wt. %
Brines
[0038] In an embodiment, various brines were made by mixing sodium chloride and calcium chloride in deionized water. In an embodiment, a brine can contain one or more of sodium chloride, calcium chloride, potassium chloride, magnesium chloride, sodium sulfate, and potassium sulfate.
TABLE-US-00002 Brines #1-5 Brine #1 Brine #2 Brine #3 Brine #4 Brine #5 NaCl (wt %) 3.0 10.0 15.0 20.0 10.0 CaCl.sub.2 (wt%) 0.5 0.5 0.5 0.5 2.0
Example 1. Wettability Tests
[0039] As illustrated in
Example 2. Thermal Stability Tests
[0040] Thermal stability of the surfactant solutions was tested by comparing the interfacial tensions of the surfactant solutions both aged and unaged at 320° F. for 4 days with a “KRUSS spinning drop tensiometer SDT”. The interfacial tensions were measured between Brine #1 with 1 gpt surfactant solution #1 and crude oil with an API gravity of 41.7 degrees as the temperature increased from room temperature to 176° F. and maintained at 176° F.
Example 3. Salinity and Hardness Compatibility Tests
[0041] The salinity and hardness compatibility of the surfactant solutions was tested by measuring the interfacial tensions between crude oil and brine with 1 gpt surfactant solutions and different salinity and hardness. The API gravity of the crude oil is 41.7 degrees.
Example 4. Oil Recovery Tests
[0042] Spontaneous imbibition tests were used to evaluate the performance of the surfactant solutions on improving and increasing oil recovery. Parker sandstone cores with porosity and permeability about 14% and 6 md respectively were used for the spontaneous imbibition tests. The cores were dried for 24 hours at 176° F., saturated with crude oil with an API gravity of 41.7°, aged at 176° F. for 3 weeks, and then used for the spontaneous imbibition tests.
[0043] All of the compositions and methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this disclosure have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the compositions and methods and in the steps or in the sequence of steps of the methods described herein without departing from the concept, spirit and scope of the disclosure. More specifically, it will be apparent that certain agents which are both chemically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the disclosure as defined by the appended claims.