Patent Application
20210214509
The present invention belongs to the technical field of oil field exploitation, and more specifically relates to a lignocellulose nanofibril material, a stable foam system based thereon, a preparation method and an application thereof.
Foam is a heterogeneous system formed by gas, surfactant and water. Foam is widely used in oil displacement, profile control, water control, anti-gas channeling, fracturing, and other aspects because foam concurrently possesses the features of low density, small weight and certain viscosity, and is capable of flowing continuously to carry water, oil and sand. However, foam is a thermodynamic metastable system. The space occupied by the foam liquid film will spontaneously decrease to reduce the overall surface free energy of the system to maintain its own stability. From a long-term perspective, the collapse of foam is irreversible.
Currently, foam stabilizers mainly include high molecular weight polymers and solid-phase nanomaterials. Nevertheless, the large-scale promotion and application of foam stabilizers in the oil field are greatly limited by the problems of their properties, cost, and sources. Cellulose nanofibril (CNF), separated from plant cellulose, is a kind of filamentous fibers with a diameter of 5-20 nm and a length ranging from several hundred nanometers to several micrometers, which is also one of the most widespread natural polysaccharide polymer materials in nature. As the basic unit of cellulose fiber, the cellulose nanofibril not only has the properties of cellulose, but also has numerous properties of nanomaterials such as large specific surface, strong hydrophilicity, easy modification, high stability, and the like. Therefore, cellulose nanofibrils have good application potential in stabilizing the foam liquid film.
The abilities of ordinary cellulose nanofibrils (CNF) and modified fiber materials on stabilizing foams have been studied at present, which substantiates that amphiphilic CNFs work best. However, such fiber materials need to be grafted with two types of groups together, their processing procedure is complicated, and the production cost is high, thereby limiting the field application of oil fields.
Therefore, developing a low-cost fiber material with similar effects has great significance and practical value for the wide application of foam systems in oil field production.
For the above problems in the prior art, the present disclosure provides a lignocellulosic nanofibril material, a stable foam system based thereon, a preparation method and an application thereof, which can effectively solve the problems of poor foam stability and high cost in the prior art.
To achieve the above objective, the present invention uses the following technical solutions to solve the technical problems.
A lignocellulosic nanofibril material includes the following components: 0.5-20 wt % of wood flour, 0.1-10 wt % of (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl (TEMPO), 2-25 mmol/g of an oxidant, 6-15 wt % of NaBr, and a balance of water.
Further, the lignocellulosic nanofibril material includes the following components: 15 wt % of the wood flour, 5 wt % of TEMPO, 10 mmol/g of the oxidant, 12 wt % of NaBr, and a balance of water.
Further, the wood flour has a particle size of 20-120 mesh, and the oxidant is NaClO or NaClO2.
A method for preparing the above-mentioned lignocellulosic nanofibril material includes the following steps:
(1) dispersing the wood flour evenly in water, then adding TEMPO and NaBr and adjusting the pH of the reaction system to 10-10.5, followed by adding oxidant, keeping the pH of the reaction system constant during the reaction, performing the reaction for 0.5-4 h, and finally, washing to obtain an oxidized fiber;
(2) adding the oxidized fiber to water, allowing a concentration of the oxidized fiber to be 0.5-10 wt %, and then performing a homogenization treatment by a high-pressure homogenizer with a homogenization pressure of 40-150 MPa and a homogenization number of 1-20 times to obtain the lignocellulosic nanofibril material (LCNF).
Further, in the oxidized fiber, a content of carboxyl group is 0.3-2.5 mol/L and a content of lignin is 0.1-40 wt %.
A stable foam system based on a lignocellulosic nanofibril material includes the following components in mass percentage:
0.1-1.0 wt % of the lignocellulosic nanofibril material, 0.2-1.0 wt % of a surfactant, 0.1-10 wt % of sodium chloride, 0.1-1.0 wt % of calcium chloride, 0.1-1.0 wt % of magnesium chloride, 0.1-1.0 wt % of sodium sulfate is, and a balance of water.
Further, the stable foam system based on the lignocellulosic nanofibril material includes the following components in mass percentage: 0.1-0.4 wt % of the lignocellulosic nanofibril material, 0.2-1.0 wt % of the surfactant, 0-4.2 wt % of sodium chloride, 0-0.7 wt % of calcium chloride, 0-0.42 wt % of magnesium chloride, 0-0.04 wt % of sodium sulfate, and a balance of water. Preferably, the stable foam system includes 0.1 wt % of the lignocellulosic nanofibril material, 0.4 wt % of the surfactant, 3.44 wt % of sodium chloride, 0.64 wt % of calcium chloride, 0.18 wt % of magnesium chloride, 0-0.018 wt % of sodium sulfate, and a balance of water.
Further, the surfactant is a mixture of sodium secondary alkyl sulfonate and α-alkenyl sulfonate mixed at a molar ratio of 1:1.
A method for preparing the above-mentioned stable foam system based on the lignocellulosic nanofibril material includes the following steps:
(1) dissolving sodium chloride, calcium chloride, magnesium chloride and sodium sulfate in deionized water and stirring evenly;
(2) dissolving a surfactant in the solution obtained in step (1) and stirring evenly;
(3) dispersing the lignocellulosic nanofibril material into the solution obtained in step (2) and stirring evenly; and
(4) bubbling air into the solution obtained in step (3) until the foam volume no longer increases to obtain the stable foam system.
The above-mentioned stable foam system based on the lignocellulosic nanofibril material can be used in oil field exploitation, such as profile control, coning control, fracturing, well drilling, foam scrubbing, etc.
In the present invention, the lignocellulose nanofibril material, the stable foam system based thereon, and the preparation method and application thereof have the following advantages.
The wood flour used in the present invention is sawdust waste produced in the wood processing industry in the market. In order to maximize benefits, the present invention directly mixes the wood flour with oxidants, NaBr, and TEMPO for reaction without any chemical treatment. The process is simple, the cost is low, and all lignin is retained in the prepared cellulose nanofibril material. The reaction mechanism is as follows. There are a large number of primary alcohol hydroxyl groups in wood flour. NaClO is the main oxidant in this process, which first forms NaBrO with NaBr. Then, NaBrO oxidizes TEMPO to nitrosonium ions. The nitrosonium ions oxidize the primary alcohol hydroxyl groups in the wood flour to form aldehyde groups (intermediates), and finally, carboxyl groups are generated. The specific reaction formula is as follows:
The obtained lignocellulose nanofibril material is used as an important component of the foam system, which cooperates with other components to obtain the foam with good stability. The drainage half-life can be increased by 1.5 times, the foam service life can be doubled, and the drag coefficient and residual drag coefficient can be increased by 5 times.
A lignocellulosic nanofibril material includes the following components: 15 wt % of needlebush wood flour, 5 wt % of (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl (TEMPO), 10 mmol/g of NaClO, 12 wt % of NaBr, and a balance of water; wherein, the particle size of the needlebush wood flour is 50-100 mesh.
A method for preparing the above-mentioned lignocellulosic nanofiber material includes the following steps.
(1) The needlebush wood flour is evenly dispersed into water and the concentration of the needlebush wood flour is controlled to be 15 wt %. Then, TEMPO and NaBr are added and the pH of the reaction system is adjusted to be 10-10.5, followed by adding NaClO. During the reaction, the pH value of the reaction system is kept constant, the reaction is performed for 4 hours. Finally, an oxidized fiber is obtained after washing.
(2) The oxidized fiber is added to water and the concentration of the oxidized fiber is controlled to be 5 wt %. Then, a homogenization treatment is performed by a high-pressure homogenizer with a homogenization pressure of 50 MPa and a homogenization number of 10 times to obtain the lignocellulosic nanofibril material (LCNF-1).
By a TAPPI T 222 om-11 (2011) method, the lignin content in the LCNF-1 was determined to be 15.5 wt %.
The dosage of NaClO in the above components is changed to be 13 mmol/g, and the remaining components and their contents are not changed. A lignocellulosic nanofibril material is obtained according to the above preparation process and is denoted as LCNF-2 with a lignin content of 11.7%.
The dosage of NaClO in the above components is changed to be 18 mmol/g, and the remaining components and their contents are not changed. A lignocellulosic nanofibril material is obtained according to the above preparation process and is denoted as LCNF-3 with a lignin content of 8.66%.
The dosage of NaClO in the above components is changed to be 25 mmol/g, and the remaining components and their contents are not changed. A lignocellulosic nanofibril material is obtained according to the above preparation process and is denoted as LCNF-4 with a lignin content of 4.49%.
The lignocellulosic nanofibril material in embodiment 1 is used to prepare a stable foam system. The foam system includes the following components in mass percentage: 0.1 wt % of the LCNF-1, 0.4 wt % of a surfactant, 3.44 wt % of sodium chloride, 0.64 wt % of calcium chloride, 0.18 wt % of magnesium chloride, 0.018 wt % of sodium sulfate, and a balance of water; wherein, the surfactant is a mixture of sodium secondary alkyl sulfonate and α-alkenyl sulfonate mixed at a molar ratio of 1:1.
A method for preparing the above-mentioned stable foam system includes the following steps.
(1) At room temperature, sodium chloride, calcium chloride, magnesium chloride and sodium sulfate are dissolved in deionized water and stirred evenly.
(2) At room temperature, the surfactant is dissolved in the solution obtained in step (1) and stirred evenly.
(3) At room temperature, the lignocellulosic nanofibril material is dissolved in the solution obtained in step (2) and stirred evenly until no obvious flocculent precipitate is present.
(4) The solution obtained in step (3) is transferred to a foam meter, and air is blown in from the bottom until the foam volume no longer increases, so as to obtain the stable foam system.
A stable foam system based on a lignocellulosic nanofibril material includes the following components in mass percentage: 0.1 wt % of the LCNF-2, 0.4 wt % of a surfactant, 3.44 wt % of sodium chloride, 0.64 wt % of calcium chloride, 0.18 wt % of magnesium chloride, 0.018 wt % of sodium sulfate, and a balance of water; wherein, the surfactant is a mixture of sodium secondary alkyl sulfonate and α-alkenyl sulfonate mixed at a molar ratio of 1:1.
A method for preparing the above-mentioned stable foam system includes the following steps.
(1) At room temperature, sodium chloride, calcium chloride, magnesium chloride and sodium sulfate are dissolved in deionized water and stirred evenly.
(2) At room temperature, the surfactant is dissolved in the solution obtained in step (1) and stirred evenly.
(3) At room temperature, the lignocellulosic nanofibril material is dissolved in the solution obtained in step (2) and stirred evenly until no obvious flocculent precipitate is present.
(4) The solution obtained in step (3) is transferred to a foam meter, and air is blown in from the bottom until the foam volume no longer increases, so as to obtain the stable foam system.
A stable foam system based on a lignocellulosic nanofibril material includes the following components in mass percentage: 0.1 wt % of the LCNF-3, 0.4 wt % of a surfactant, 3.44 wt % of sodium chloride, 0.64 wt % of calcium chloride, 0.18 wt % of magnesium chloride, 0.018 wt % of sodium sulfate, and a balance of water; wherein, the surfactant is a mixture of sodium secondary alkyl sulfonate and α-alkenyl sulfonate mixed at a molar ratio of 1:1.
A method for preparing the above-mentioned stable foam system includes the following steps.
(1) At room temperature, sodium chloride, calcium chloride, magnesium chloride and sodium sulfate are dissolved in deionized water and stirred evenly.
(2) At room temperature, the surfactant is dissolved in the solution obtained in step (1) and stirred evenly.
(3) At room temperature, the lignocellulosic nanofibril material is dissolved in the solution obtained in step (2) and stirred evenly until no obvious flocculent precipitate is present.
(4) The solution obtained in step (3) is transferred to a foam meter, and air is blown in from the bottom until the foam volume no longer increases, so as to obtain the stable foam system.
A stable foam system based on a lignocellulosic nanofibril material includes the following components in mass percentage: 0.1 wt % of the LCNF-4, 0.4 wt % of a surfactant, 3.44 wt % of sodium chloride, 0.64 wt % of calcium chloride, 0.18 wt % of magnesium chloride, 0.018 wt % of sodium sulfate, and a balance of water; wherein, the surfactant is a mixture of sodium secondary alkyl sulfonate and α-alkenyl sulfonate mixed at a molar ratio of 1:1.
A method for preparing the above-mentioned stable foam system includes the following steps.
(1) At room temperature, sodium chloride, calcium chloride, magnesium chloride and sodium sulfate are dissolved in deionized water and stirred evenly.
(2) At room temperature, the surfactant is dissolved in the solution obtained in step (1) and stirred evenly.
(3) At room temperature, the lignocellulosic nanofibril material is dissolved in the solution obtained in step (2) and stirred evenly until no obvious flocculent precipitate is present.
(4) The solution obtained in step (3) is transferred to a foam meter, and air is blown in from the bottom until the foam volume no longer increases, so as to obtain the stable foam system.
The LCNF-1 prepared in embodiment 1 and the existing CNF (purchased from Tianjin Woodelfbio Cellulose Co., Ltd., with the product name of Microfibrillated Cellulose) were tested, and the EDX spectra thereof are shown in
A porous media with a rock core almost analogous to that of sandstone in pore permeability is used. The flow of foam in the porous media is simulated to measure the pressure difference between the rock core inlet and outlet. It can be seen from the test results that under the same experimental conditions, the pressure difference generated by the LCNF-stabilized foam is significantly higher than that of the blank sample-stabilized foam (Contains only a surfactant), especially for the LCNF-3. This phenomenon indicates that the stability of the LCNF-stabilized foam in the porous media is better.
The interfacial elasticity of a foam can suppress the foam coarsening and the collapse of the foam skeleton, thereby improving the stability of the foam. In the present invention, the dilational elasticity and viscosity at the gas-liquid interface of the foams are measured, and the measurement results are shown in Table 1.
As can be seen from Table 1, the interfacial elasticity of the LCNF-stabilized foams is 1.4-2.3 times higher than that of the ordinary foam, indicating that the stability of the LCNF-stabilized foams is good.
In the present invention, a foam scan instrument is used to measure the stability parameters of the foams, and the measurement results are shown in Table 2.
It can be known from Table 2 that the stability index of the LCNF-stabilized foams is significantly higher than that of the blank sample-stabilized foam, which is increased by 4.1-5.2 times relative to the blank sample-stabilized foam, indicating that the LCNF-stabilized foams have a good stability.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201910160551.7 | Mar 2019 | CN | national |
This application is the national phase entry of International Application No. PCT/CN2019/082782, filed on Apr. 15, 2019, which is based upon and claims priority to Chinese Patent Application No. 201910160551.7, filed on Mar. 4, 2019, the entire contents of which are incorporated herein by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/082782 | 4/15/2019 | WO | 00 |
