MODIFIED MOS2 NANO MATERIAL, AND PREPARATION METHOD AND USE THEREOF

Abstract

The invention provides a modified MoS.sub.2 nano material and a preparation method thereof. The modified MoS.sub.2 nanomaterial is comprised of a hydrophilic MoS.sub.2 nanosheet linked with hydrophobic alkyl amine chain, the hydrophobic alkyl amine chain is provided by an alkylamine compound. The modified MoS.sub.2 nano material provided by the invention can be formulated into a nanofluid i.e. oil-displacement agent at a lower concentration, and is applied to the tertiary recovery in oil recovery, thereby greatly reducing the environmental pollution in the tertiary recovery, reducing the cost and improving the oil recovery.

Claims

1. A modified MoS.sub.2 nanomaterial, characterized in that the modified MoS.sub.2 nanomaterial is comprised of a hydrophilic MoS.sub.2 nanosheet linked with hydrophobic alkyl amine chain, the hydrophobic alkyl amine chain is provided by an alkylamine compound.

2. A modified MoS.sub.2 nanomaterial according to claim 1, characterized in that the modified MoS.sub.2 nanomaterial is prepared by the following steps: adding a hydrophilic MoS.sub.2 nanosheet into an organic solution of the alkylamine compound, and stirring at 50-200 rpm for 6-15 hours at 25 C., and colleting a precipitate, the obtained precipitate is the modified MoS.sub.2 nano material; the amount of the hydrophilic MoS.sub.2 nanosheet is 1-10 wt % and the amount of the alkylamine compound is 0.1-5 wt % per 100 mL of the organic solution.

3. The modified MoS.sub.2 nanomaterial according to claim 1, wherein the alkylamine compound is one or more of butylamine, octylamine and dodecylamine.

4. The modified MoS.sub.2 nanomaterial according to claim 1, wherein the modified MoS.sub.2 nanomaterial is in the form of nanoscale sheet.

5. The modified MoS.sub.2 nanomaterial according to claim 4, wherein the modified MoS.sub.2 nanomaterial has a thickness of 1-1.2 nm.

6. The modified MoS.sub.2 nanomaterial according to claim 4, wherein a size of the modified MoS.sub.2 nanomaterial is 100 nm.

7. A nanofluid, characterized in that the nanofluid is obtained by mixing the modified MoS.sub.2 nanomaterial of claim 1 with a stabilizer in saline or deionized water; the amount of the modified MoS.sub.2 nano material is 50-1000 ppm and the amount of the stabilizer is 20-1000 ppm per 100 mL of the saline water or deionized water; the concentration of the saline water is 10,000-220000 mg/L.

8. The nanofluid according to claim 7, wherein the stabilizer is one or more of polyvinylpyrrolidone, alkyl polyoxyethylene ether and poly(sodium-p-styrenesulfonate).

9. The nanofluid according to claim 7, wherein the modified MoS.sub.2 nanomaterial and the stabilizer are mixed in saline or deionized water under ultrasonic condition at a stirring speed of 50-200 rpm.

10. Use of the nanofluid of claim 7 in oil recovery.

11. The use according to claim 10, comprising injecting the nanofluid to a reservoir formation so as to contact with oil, then removing the oil from the reservoir formation by reducing oil interfacial surface tension and changing wettability of the reservoir formation.

12. A method of preparing a modified MoS.sub.2 nanomaterial, characterized in, comprising the following steps: 1) adding a molybdenum source, a sulfur source, and a reducing agent into water to obtain a reaction mixture; 2) stirring the reaction mixture at a speed of 100-500 rpm under 1-5 bar; 3) then reacting the reaction mixture at 150-250 C. for 6-15 hours to obtain a precipitate, the obtained precipitate is the hydrophilic MoS.sub.2 nanosheet; 4) adding the hydrophilic MoS.sub.2 nanosheet obtained in step 3) into an organic solution of alkylamine compound, stirring at 50-200 rpm for 6-15 hours at 25 C., and collecting a precipitate, the obtained precipitate is the modified MoS.sub.2 nanomaterial; wherein the amount of the hydrophilic MoS.sub.2 nanosheet is 1-10 wt % and the amount of the alkylamine compound is 0.1-5 wt % per 100 mL of the organic solution.

13. The method of preparing a modified MoS.sub.2 nanomaterial according to claim 12, wherein in step 1), the amount of the molybdenum source is 30-80 mmol, the amount of the sulfur source is 30-160 mmol, the reduction and the amount of the agent is 0.8-1 mol per 100 mL of the water.

14. The method of preparing a modified MoS.sub.2 nanomaterial according to claim 12, wherein: the molybdenum source is one or more of ammonium molybdate, molybdenum pentachloride and molybdenum oxide; the sulfur source is one or more of thioacetamide, sodium sulfonate and potassium thiocyanate; the reducing agent is one or more of urea, ascorbic acid and hydrazine.

15. The method of preparing a modified MoS.sub.2 nanomaterial according to claim 13, wherein: the molybdenum source is one or more of ammonium molybdate, molybdenum pentachloride and molybdenum oxide; the sulfur source is one or more of thioacetamide, sodium sulfonate and potassium thiocyanate; the reducing agent is one or more of urea, ascorbic acid and hydrazine.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0049] FIG. 1 shows a high resolution TEM (transmission electron microscope) image of hydrophilic MoS.sub.2 nanosheet (1T-MoS.sub.2) prepared in accordance with the present invention.

[0050] FIG. 2 shows the Raman spectrum of the hydrophilic MoS.sub.2 nanosheet (1T-MoS.sub.2) prepared in accordance with the present invention.

[0051] FIG. 3 shows an SEM (scanning electron microscope) image of the modified MoS.sub.2 nanosheet prepared in accordance with the present invention.

[0052] FIG. 4A shows an AFM (atomic force microscope) image of modified MoS.sub.2 nanosheets prepared in accordance with the present invention. FIG. 4B shows a histogram of thickness across various location of the AFM image of FIG. 4A.

[0053] FIG. 5 shows the FTIR spectrum of the three materials of the present invention.

[0054] FIG. 6A shows the static contact angle of the hydrophilic MoS.sub.2 nanosheet prepared by the present invention with 5 L of water droplets; FIG. 6B shows the static contact angle of the modified MoS.sub.2 nanomaterial prepared by the present invention with 5 L of water droplets.

[0055] FIG. 7A shows an oil/saline system in a test tube without the addition of MoS.sub.2 at the oil/saline water interface; FIG. 7B shows the oil/saline system in a test tube with the addition of the hydrophilic MoS.sub.2 nanosheets prepared in accordance with the present invention at the oil/saline water interface; FIG. 7C shows an oil/saline system in a test tube with the addition of the modified MoS.sub.2 nanosheets prepared in accordance with the present invention at the oil/saline water interface.

[0056] FIG. 8 shows an interfacial tension vs. time plot of nanofluids 801-803 (nanofluids prepared using deionized water).

[0057] FIG. 9 shows an interfacial tension vs. time plot of nanofluids 901-903 (nanofluids prepared using saline water).

[0058] FIG. 10 shows the stability of the nanofluid 803.

[0059] FIG. 11 shows the stability of the nanofluid 903.

[0060] FIG. 12 shows the core flooding experimental setup.

[0061] FIG. 13 shows a visual model of oil recovery.

DETAILED DESCRIPTION

Example 1

[0062] Preparation of the Modified MoS.sub.2 Nanomaterial of the Invention

[0063] 1) adding ammonium molybdate (molybdenum source), potassium thiocyanate (sulfur source) and ascorbic acid (reducing agent) into water to obtain a reaction mixture; wherein the amount of the molybdenum source is 70 mmol, the amount of the sulfur source is 140 mmol, and the amount of the reducing agent is 1 mol per 100 mL of water; 2) stirring the reaction mixture at 450 rpm in a hydrothermal autoclave for 1-3 hours at a pressure of 3 bar;

[0064] 3) then reacting the reaction mixture at 180 C. for 12 hours to obtain a precipitate, after the obtained precipitate is collected and cooled to room temperature, washed with water and ethanol, and then dried at 80 C., the resulting precipitate is the hydrophilic MoS.sub.2 nanosheet; 4) adding the hydrophilic MoS.sub.2 nanosheet obtained in step 3) into an anhydrous ethanol solution of dodecylamine, and stirring at 60 rpm for 15 hours at 25 C., wherein the amount of the hydrophilic MoS.sub.2 nanosheet is 3 wt %, the amount of the dodecylamine is 0.5 wt % per 100 mL of the anhydrous ethanol solution, and collecting a precipitate, the obtained precipitate is washed with water and ethanol, and then dried at 80 C. for about 6 hours, the resulting precipitate is the modified MoS.sub.2 nanosheet.

[0065] The hydrophilic MoS.sub.2 nanosheets and modified MoS.sub.2 nanosheets are identified by the conventional methods in the art.

[0066] The high-resolution transmission electron microscope is performed to examine the structure of the hydrophilic MoS.sub.2 nanosheets of the present invention. FIG. 1 shows a high resolution TEM (transmission electron microscope) image of a hydrophilic MoS.sub.2 nanosheet prepared in accordance with the present invention. The rectangular area in FIG. 1 shows the edge of the hydrophilic MoS.sub.2 nanosheet with multiple layers. It can be seen that the spacing between the layers is 0.64-0.65 nm, which is consistent with the known interlayer spacing of MoS.sub.2 (0.64 nm).

[0067] Raman spectroscopy is used to determine the polymorphic nature of the synthesized nanosheets. FIG. 2 shows the raman spectrum of the hydrophilic MoS.sub.2 nanosheet (1T-MoS.sub.2) prepared in accordance with the present invention. In FIG. 2, the E.sub.1g and A.sub.1g vibration modes observed at 284 cm.sup.1 and 407 cm.sup.1 proves the presence of 1T-MoS.sub.2 having an octahedral structure. The vibrational modes observed at 146 cm.sup.1(J.sub.1), 226 cm.sup.1(J.sub.2) and 333 cm.sup.1(J.sub.3) proves the presence of a superlattice on the basal plane of single layer MoS.sub.2, indicating the prepared hydrophilic MoS.sub.2 nanosheet in accordance with the present invention is 1T-MoS.sub.2.

[0068] FIG. 3 shows an SEM (scanning electron microscope) image of the modified MoS.sub.2 nanosheet prepared in accordance with the present invention. It can be seen that the modified MoS.sub.2 nanosheet has a size of about 100 nm, and the zoomed area shows that the modified MoS.sub.2 nanosheet resembles like coral reef

[0069] AFM images are used to show the thickness characteristics of the nanosheet. FIG. 4A shows an AFM (atomic force microscope) image of the modified MoS.sub.2 nanosheet prepared in accordance with the present invention, a typical tapping mode AFM image of the modified MoS.sub.2 nanosheet deposited on a SiO.sub.2 substrate by spin coating can be seen from FIG. 4A. FIG. 4B shows a histogram of thickness across various location of the AFM image of FIG. 4A. It can be seen from FIG. 4B, the measured thickness of the modified MoS.sub.2 nanosheet is found to be around 1 to 1.2 nm across various location.

[0070] FIG. 5 shows the FTIR spectrum of the three materials of the present invention. Wherein 501 shows the spectrum of the alkyl amine compound, the bands at 2922 cm.sup.1 and 2853 cm.sup.1 are the asymmetric and symmetric vibrations of CH.sub.2 in the alkyl amine group, respectively, and the peak at 1572 cm.sup.1 is due to the NH scissoring of the amine group, while 1470 cm.sup.1 was due to CN stretch of the amide. 502 shows the spectrum of the modified MoS.sub.2 nanosheets, indicating that the alkyl amine chain is located on the surface of the nanosheet. 503 shows the FTIR spectrum of MoS.sub.2, the peaks at 420 cm.sup.1, 620 cm.sup.1, 761 cm.sup.1, 908-956 cm.sup.1 represent the out-of-plane vibration of S atom, the vibration of SH, the vibration of MoS, and vibration of MoO.

Example 2

[0071] Preparation of the Modified MoS.sub.2 Nanomaterial of the Invention

[0072] 1) adding molybdenum pentachloride (molybdenum source), sodium sulfonate (sulfur source) and hydrazine (reducing agent) into water to obtain a reaction mixture; the amount of the molybdenum source is 30 mmol, and the amount of the sulfur source is 30 mmol, the amount of the reduction agent is 0.8 mol per 100 mL of water;

[0073] 2) stirring the reaction mixture at 250 rpm for 1-3 hours under an oil bath at a pressure of 5 bar;

[0074] 3) then reacting the reaction mixture at 200 C. for 8 hours to obtain a precipitate, and the obtained precipitate is collected and cooled to room temperature, washed with water and ethanol, and then dried at 80 C. for about 6-8 hours, the resulting precipitate is the hydrophilic MoS.sub.2 nanosheet.

[0075] 4) adding the hydrophilic MoS.sub.2 nanosheet obtained in step 3) into an anhydrous ethanol solution of butylamine, and stirring at 100 rpm for 12 hours at 25 C., wherein the amount of the hydrophilic MoS.sub.2 nanosheet is 5 wt %, the amount of the butylamine was 1 wt % per 100 mL of the anhydrous ethanol solution, and collecting a precipitate, the obtained precipitate is washed with water and ethanol, and then dried at 80 C. for about 8 hours, the resulting precipitate is the modified MoS.sub.2 nanosheet.

[0076] The surface properties of the hydrophilic MoS.sub.2 nanosheets and modified MoS.sub.2 nanosheets are measured using the contact angle measurement. Generally, a surface having a contact angle between 0 and 90 is a hydrophilic surface, and a surface having a contact angle of 90 to 180 is a hydrophobic surface. The octahedral arrangement of Mo and S atoms results in the MoS.sub.2 nanosheet having a contact angle of 42 and reflects the hydrophilic behavior (FIG. 6A).

[0077] FIG. 6A shows the static contact angle of the hydrophilic MoS.sub.2 nanosheet of the present invention with 5 L of the water droplet; FIG. 6B shows the static contact angle of the modified MoS.sub.2 nanomaterial of the present invention with 5 L of the water droplet, and it can be seen that the contact angle was changed to 91 after modification with an alkylamine, which resulted in the MoS.sub.2 nanosheets possess amphiphilicity after the modification (FIG. 6B).

Example 3

[0078] Preparation of Modified MoS.sub.2 Nanomaterial of the Invention

[0079] 1) adding molybdenum oxide (molybdenum source), thioacetamide (sulfur source) and urea (reducing agent) into water to obtain a reaction mixture; the amount of the molybdenum source is 50 mmol, the amount of the sulfur source is 100 mmol, and the amount of the reducing agent is 1 mol per 100 mL of water;

[0080] 2) stirring the reaction mixture at 500 rpm for 1-3 hours at 200 C. under a pressure of l bar;

[0081] 3) then reacting the reaction mixture at 250 C. for 14 hours to obtain a precipitate, and the obtained precipitate is collected and cooled to room temperature, washed with water and ethanol, and then dried at 80 C. for about 9 hours, the resulting precipitate is the hydrophilic MoS.sub.2 nanosheet.

[0082] 4) adding the hydrophilic MoS.sub.2 nanosheet obtained in step 3) into a toluene solution of octylamine, and stirring at 180 rpm for 6 hours at 25 C., wherein the amount of the hydrophilic MoS.sub.2 nanosheet is 10 wt %, the amount of the octylamine is 5 wt % per 100 mL of the toluene solution, and the collecting a precipitate, the obtained precipitate is washed with water and ethanol, and then dried at 80 C. for about 10 hours, the resulting precipitate is the modified MoS.sub.2 nanosheet (that is, amphoteric MoS.sub.2 nanosheets).

[0083] The hydrophilic MoS.sub.2 nanosheets and the amphoteric MoS.sub.2 nanosheets prepared in this example are used to test on the oil/saline water interface. FIG. 7A shows an oil/saline system in a test tube without the addition of MoS.sub.2 at the oil/saline water interface; FIG. 7B shows the oil/saline system in a test tube with the addition of the hydrophilic MoS.sub.2 nanosheets prepared in accordance with the present invention at the oil/saline water interface; FIG. 7C shows an oil/saline system in a test tube with the addition of the modified MoS.sub.2 nanosheets prepared in accordance with the present invention at the oil/saline water interface. Due to the high interfacial surface tension between the oil and saline water, a concave interface is generated at the oil/saline water interface, as shown in FIG. 7A. When the modified MoS.sub.2 nanosheets prepared according to the present invention were gently injected to the oil/saline water system, the interfacial tension was reduced and the concave region of oil/saline water interface is transformed to flat, as shown in FIG. 7C. When the unmodified nanosheets (that is the hydrophilic MoS.sub.2 nanosheets) are injected to the oil/saline water system, the hydrophilic MoS.sub.2 nanosheets dispersed in the saline water and settle down a few minutes later, as shown in FIG. 7B.

Example 4

[0084] 1. The Preparation of Nanofluids

[0085] 1) Preparation of nanofluid 801: it is obtained by mixing the modified MoS.sub.2 nanomaterial with the polyvinylpyrrolidone (stabilizer) in deionized water; the amount of the modified MoS.sub.2 nanomaterial is 500 ppm (i.e. 0.05 wt. %) and the amount of the stabilizer is 1000 ppm per 100 mL of deionized water, the nanofluid was named as nanofluid 801.

[0086] 2) The method of preparing the nanofluid 802 is the same as that of nanofluid 801, except that the amount of the modified MoS.sub.2 nanomaterial is 1000 ppm (i.e., 0.1 wt %), and the amount of the stabilizer is 100 ppm, the stabilizer agent is poly (sodium-p-styrenesulfonate).

[0087] 3) The method of preparing the nanofluid 803 is the same as that of the nanofluid 801, except that the amount of the modified MoS.sub.2 nanomaterial is 50 ppm (i.e., 0.005 wt %), and the amount of the stabilizer is 50 ppm, the stabilizer agent is alkyl polyoxyethylene ether.

[0088] 4) The method of preparing the nanofluid 901 is the same as that of the nanofluid 801, except that the deionized water is replaced with saline water, and the concentration of the saline water is 10000 mg/L.

[0089] 5) The method of preparing the nanofluid 902 is the same as that of the nanofluid 802, except that the deionized water is replaced with saline water, and the concentration of the saline water is 10000 mg/L.

[0090] 6) The method of preparing the nanofluid 903 is the same as that of the nanofluid 803, except that the deionized water is replaced with saline water, and the concentration of the saline water is 10000 mg/L, and the modified MoS.sub.2 nanomaterial and the stabilizer are mixed in saline or deionized water under ultrasonic condition at a stirring speed of 50-200 rpm.

[0091] 7) The nanofluid 803, the method of preparing the nanofluid 803 is the same as that of the nanofluid 803, except that the stabilizer is not used in the preparation process.

[0092] 8) The nanofluid 903, the method of preparing the nanofluid 903 is the same as that of the nanofluid 903, except that the stabilizer is not used in the preparation process.

[0093] II . Interfacial Tension and Stability of Nanofluids

[0094] The interfacial tension between the oil and the nanofluid prepared above is tested using a tensiometer at 30 C. The stability of the nanofluid of the present invention was measured by transmission and backscattering of pulsed near-infrared light (=880 nm) by using a Turbiscan Lab Expert of Formulaction. The Stability Dynamics Index (TSI) is used to evaluate the stability of nanofluids. A higher TSI value indicates a less stable fluid.

[0095] FIG. 8 shows an interfacial tension vs. time plot of nanofluids 801-803 (nanofluids prepared using deionized water). It is apparent from FIG. 8, the nanofluid 803 achieves a minimum interfacial surface tension of 0.5 mN/m.

[0096] FIG. 9 shows an interfacial tension vs. time plot of nanofluids 901-903 (nanofluids prepared using saline water). It is apparent from FIG. 9, the nanofluid 903 achieves a minimum interfacial surface tension of 0.1 mN/m.

[0097] FIG. 10 shows the stability of the nanofluid 803. The curve 1001 represents the TSI value curve of the nanofluid 803 (the nanofluid 803 differs from the nanofluid 803 in that the preparation process does not use a stabilizer), and the curve 1002 represents the TSI value curve of the nanofluid 803. 1002 shows less TSI values, which indicates the better stability performance compared to 1001.

[0098] FIG. 11 shows the stability of the nanofluid 903. The curve 1101 represents the TSI value curve of the nanofluid 903 (the nanofluid 903 differs from the nanofluid 903 in that the preparation process does not use a stabilizer), and the curve 1102 represents the TSI value curve of the nanofluid 903. 1102 shows less TSI values, which indicates the better stability performance compared to 1101.

[0099] As can be seen from FIGS. 10-11, the nanofluid prepared using saline water can achieve better stability after using the stabilizer. Therefore, the nanofluid of the present invention can be prepared with the seawater present near the reservoirs which leads to the decrease in cost of the water consumption.

Example 5

[0100] The core flooding experiment was carried out by using the nanofluid 803 and nanofluid 903 synthesized in the present invention to verify the oil recovery rate of the modified MoS.sub.2 nanomaterial of the present invention in the tertiary recovery stage.

[0101] Core flooding experiments are done using man-made sandstone cores and tested in the flooding equipment (shown in FIG. 12). The physical properties of the core samples are shown in Table 1. Before flooding, the cores are all cleaned throughout and saturated in water for 24 hours. Then the oil having a viscosity of 50 cP (high viscosity oil) is pumped into the core so that no more water is flowing out (i.e., the core is 100% saturated with oil). After the oil saturation, water was injected at a rate of 0.5 mL/min until no more oil is recovered (secondary flooding). Finally, the nanofluid was pumped into the core at a rate of 0.5 mL/min until the remaining oil is recovered (tertiary flooding).

TABLE-US-00002 TABLE 1 Physical properties of core samples Length of Diameter of Average fluid Pore Name of the core the core permeability Porosity volume the core (cm) (cm) (mD) (%) (cm.sup.3) L1 10.02 5.02 8.7 13.050 6.40 H1 10.01 5.01 154 21.343 8.9 L2 10.01 5.00 8.65 13.106 6.43 H2 10.02 5.05 149.65 19.160 9.5 L3 10.00 5.00 8.5 13.030 6.30 H3 10.01 5.01 150 20.01 8.7

TABLE-US-00003 TABLE 2 Core flooding experiment results Oil Oil Average recovery recovery fluid rate of rate of Total perme- secondary tertiary oil Type of the Name of ability flooding flooding recovery nanofluid core (mD) (%) (%) (%) nanofluid L1 8.7 46.65 1.60 48.25 prepared H1 154 49.80 4.45 54.25 from SiO.sub.2 nanoparticles (0.01 wt %) Nanofluid L2 8.65 47.50 16.25 63.75 803 (0.005 H2 149.65 49.41 12.94 62.35 wt %) Nanofluid L3 8.5 46.80 20.50 67.30 903 (0.005 H3 150 48.04 13.80 61.84 wt %)

[0102] The data in Table 2 indicates that for high viscosity oil (e.g., 50 cP), using the nanofluids prepared by the modified MoS.sub.2 nanomaterials provided by the present invention (where the modified MoS.sub.2 nanomaterials are only used at a concentration of 0.005 wt %), both the low permeability core (e.g.,8.5-8.7 mD) and high permeability cores (e.g., 149-154 mD) have higher oil recovery rates of 13.8%-20.5% in tertiary flooding; whereas oil recovery rates of the nanofluid prepared from SiO.sub.2 nanoparticles of the prior art (produced by dissolving SiO.sub.2 nanoparticles in water, the final concentration of SiO.sub.2 nanoparticles is 0.01 wt %, and the SiO.sub.2 nanoparticles are purchased from Sigma Aldrich) is only 1.6-4.45%.

[0103] Further, nanofluids prepared from prior art SiO.sub.2 nanoparticles achieve higher oil recovery in high permeability cores (e.g., 154 mD), while the modified MoS.sub.2 nanomaterials provided by the present invention have unexpectedly higher oil recovery in low permeability cores. (e.g., 8.5-8.65 mD).

[0104] The applicant also provides a visual model of oil recovery that using the nanofluid of the present invention, as shown in FIG. 13. It can be seen from the model, the nanofluid of the present invention has a very significant recovery effect on oil in a low permeability region, the model is designed through a laser lithography technique. The geometry of the model is designed from the SEM cross section of the low permeability sandstone cores L3 (eg 8.5 mD). The three images in FIG. 13 from left to right are model images before water flooding, after water blooding and after nanofluid flooding, which clearly shows that the remaining oil in the low permeability region after the nanofluid of the present invention flooding is efficiently recovered.

[0105] Using nanofluids 801-802, 901-902 obtained from the modified MoS.sub.2 nanomaterials of the present invention to recover low viscosity crude oil, the oil recovery also can be significantly improved as that achieved for the high viscosity crude oil.