High-stability antistatic crude oil type spinning oil and preparation method thereof
By introducing alkyl modified titanium carbide sheets into the spinning oil agent, the problems of coking resistance and interface adaptability of the spinning oil agent in high-speed spinning high temperature environment are solved, and high stability and improvement of anti-static properties and production efficiency are achieved.
Patent Information
- Application Number
- CN202510752926.4
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-06-06
- Publication Date
- 2025-07-04
- Estimated Expiration
- 2045-06-06
AI Technical Summary
The existing spinning oil agents are insufficient in high-speed spinning and high-temperature environments, which is difficult to meet production needs, and cannot achieve comprehensive optimization on the interface characteristics of different fibers, resulting in fiber surface damage, breaking and low production efficiency.
The alkyl modified titanium carbide sheet is used as the core component of the antistatic agent, and combined with sodium dodecyl sulfate and sodium dodecyl sulfonate, a highly stable antistatic spinning oil agent is formed, and a conductive network is built through a two-dimensional sheet structure, reducing the use of phosphate antistatic agents, and improving the conductivity and stability of the oil agent.
It significantly improves the antistatic properties and stability of spinning oil agents, reduces coke deposits, reduces the amount of antistatic agents, and ensures the stability and efficient production of the spinning process.
Abstract
Description
Technical Field
[0001] The invention belongs to the technical field of spinning oils, and particularly relates to a highly stable antistatic crude oil type spinning oil and a preparation method thereof. Background Art
[0002] As the textile industry accelerates its move towards high value-added and functional fields, the fiber material system has shown unprecedented diversified innovation vitality. A series of differentiated varieties such as regenerated cellulose fiber, ultra-fine denier fiber, bio-based fiber and high-performance synthetic fiber have emerged like mushrooms after rain. These new fibers have their own characteristics in performance, which greatly enriches the types and application scenarios of textile products. However, their emergence also puts forward almost harsh process requirements for spinning processing technology. As a core auxiliary agent that is crucial in the spinning process, spinning oil is facing severe challenges: on the one hand, in the high-temperature environment of high-speed spinning, spinning oil needs to have excellent anti-coking performance. High temperature will cause oxidation, polymerization and other reactions of certain components in the oil. If the anti-coking property is insufficient, coking deposits will easily form. These deposits will not only cause a sharp increase in the local friction between the fiber and the equipment components, but also cause damage to the fiber surface and quality degradation in severe cases, and even cause production accidents such as broken ends and broken wires, greatly affecting production efficiency and product quality. For example, in some high-speed spinning production lines, due to the poor anti-coking property of the oil, obvious coking will occur in key parts of the equipment after several hours of operation, requiring frequent shutdowns for cleaning, which seriously restricts the production progress. On the other hand, the formula of the spinning oil also needs to be precisely controlled in view of the unique interface characteristics of different fibers. Due to the significant differences in the chemical composition, surface morphology and physical properties of different fibers, this requires the oil to optimize the anti-splashing performance while strengthening the anti-static property.
[0003] Chinese patent document CN117845379B discloses a process for preparing a highly efficient antistatic agent for chemical fiber oil, which combines the prepared nitrogen-sulfur doped Mxene with an antistatic agent to obtain a new antistatic agent. The chemical fiber oil prepared by using the antistatic agent has an electrical conductivity of about 0.775~0.988mS / cm. Although the patent introduces Mxene material into the antistatic agent, which improves the antistatic performance of the oil to a certain extent, the overall performance of the oil has not achieved a qualitative leap. On the one hand, in terms of anti-coking performance, the patented technology has not been effectively improved and optimized, and cannot meet the strict requirements for the anti-coking performance of the oil under high-speed spinning and high-temperature conditions. On the other hand, the patent has not proposed a comprehensive and systematic solution to the adaptability of different fiber interface characteristics, and it is difficult to optimize the anti-splashing performance while ensuring that the tow is tightly bundled and has no broken ends and looseness during the spinning process.
[0004] In summary, there is still an urgent need for a solution that can improve the overall performance of spinning finish. Summary of the Invention
[0005] The object of the present invention is to provide a highly stable antistatic crude oil-based spinning finish and its preparation method. Using alkyl-modified titanium carbide as the core component can not only improve the antistatic property of the highly stable antistatic crude oil-based spinning finish and reduce the total amount of antistatic components used, but also enhance the stability of the antistatic property of the spinning finish, thereby comprehensively improving the performance of the highly stable antistatic crude oil-based spinning finish.
[0006] To achieve the above object, the present technical solution provides a highly stable antistatic crude oil-based spinning finish, including: a smoothing agent, an emulsifier, an antistatic agent, a bundling agent, and a wetting agent, wherein the antistatic agent includes alkyl-modified titanium carbide sheets.
[0007] In some embodiments, the antistatic agent additionally includes one or a combination of sodium dodecyl sulfate and sodium dodecyl sulfonate.
[0008] In some embodiments, the mass content of the antistatic agent is 6-8 wt%.
[0009] This solution particularly selects alkyl-modified titanium carbide sheets as the core component of the antistatic agent. The alkyl-modified titanium carbide sheets are titanium carbide sheets with surface alkylation modification. The alkyl-modified titanium carbide sheets have a two-dimensional sheet structure and belong to a kind of alkyl-capped sheet Mxene. As the core component of the spinning finish, the alkyl-modified titanium carbide sheets in this solution can effectively enhance the overall performance of the spinning finish, including the antistatic property and stability of the spinning finish.
[0010] Furthermore, the alkyl-modified titanium carbide sheets in this solution are Ti3C2T x sheets with octyltriethoxysilane on the surface. Octyltriethoxysilane reacts with the hydroxyl groups on the surface of the titanium carbide sheets through a silane coupling agent. Due to the alkylation modification with octyltriethoxysilane in this solution, the antistatic property of the alkyl-modified titanium carbide sheets is further improved.
[0011] Specifically, the preparation method of the alkyl-modified titanium carbide sheets is as follows: S1: Prepare a titanium carbide slurry; Add LiF to the HCl solution and stir well in an ice bath to obtain a mixed solution. Slowly pour Ti3AlC2 into the mixed solution and react at 35°C - 40°C for 12 - 48 h to obtain an acidic solution. Repeatedly wash the acidic solution with deionized water by centrifugation until the pH of the supernatant is about 6 - 6.5, and exfoliate Ti3C2T through the oscillation operation during centrifugation xSheet; S2: Alkyl-modified titanium carbide sheet: Replace the water solvent of the Ti3C2Tx sheet with acetone by centrifugation and prepare a dispersion. Place the dispersion under an inert atmosphere and ultrasonicate to obtain a monolayer of Ti3C2T x acetone suspension. Add octyltriethoxysilane to the acetone suspension of monolayer Ti3C2T x and stir at room temperature for 6 - 96 h. After centrifugally washing the unreacted octyltriethoxysilane with acetone, an alkyl-modified titanium carbide sheet is obtained.
[0012] In some specific embodiments, Add 1 - 2 parts of LiF to 1 - 2 parts of HCl solution and stir well in an ice bath for 30 min to obtain a mixed solution. Slowly pour 0.05 - 0.5 parts of Ti3AlC2 into the mixed solution and react at 35°C - 40°C for 12 - 48 h to obtain an acidic solution. At this time, the Al layer is etched. Then, repeatedly wash the acidic solution with deionized water by centrifugation until the pH of the supernatant is about 6 - 6.5, and exfoliate the Ti3C2Tx sheet by oscillating during centrifugation; Disperse 0.5 - 5 g of Ti3C2T x sheets (40 wt.%) by centrifugally replacing the water solvent with acetone to prepare a 20 - 30 mL dispersion. Place the dispersion under an inert atmosphere and ultrasonicate to obtain a monolayer of Ti3C2T x acetone suspension. Add 0.5 - 5 mL of octyltriethoxysilane to the acetone suspension of monolayer Ti3C2T x and stir at room temperature for 6 - 96 h. After centrifugally washing the unreacted octyltriethoxysilane with acetone, an alkyl-modified titanium carbide sheet is obtained.
[0013] There are many advantages to using alkyl-modified titanium carbide sheets in this solution: On the one hand, it makes the spinning finish have a good anti-coking rate: In traditional spinning finishes, phosphate ester antistatic agents are often used (including the octanol phosphate salt, octanol polyoxyethylene ether phosphate salt, and dodecyl phosphate salt mentioned in the nitrogen and sulfur-doped Mxene antistatic agent in the above background). They are prone to generating coking deposits at the hot rollers during spinning processing, affecting the stability of spinning processing. In this solution, titanium carbide sheets are used as the core component of the antistatic agent, and the other antistatic agent components are selected from one or a combination of sodium dodecyl sulfate and sodium dodecyl sulfonate, without phosphate ester antistatic agents. Therefore, it can avoid the adverse effects caused by phosphate esters and improve the product quality rate.
[0014] On the other hand, the antistatic property of the spinning finish is significantly improved: Since the alkyl-modified titanium carbide sheet has a two-dimensional sheet structure, a continuous conductive network can be formed in the spinning finish. This structural feature greatly enhances the overall conductivity of the spinning finish. High conductivity means that only a small amount of antistatic agent is needed to achieve the target antistatic property, so the amount of antistatic agent can be significantly reduced.
[0015] Furthermore, the antistatic stability of the spinning finish is greatly improved: Since the original polar functional groups (such as -OH) on the surface of the titanium carbide sheet can reduce the direct contact with environmental oxygen / moisture and inhibit oxidative degradation, the lifespan of the antistatic agent can be extended from the material itself. However, the nitrogen and sulfur-doped MXene mentioned in the background art is prone to oxidation or hydrolysis during long-term use due to the exposure of surface active sites. In addition, the alkyl chain further imparts hydrophobicity to the titanium carbide sheet, reducing hygroscopicity and making the conductivity mainly depend on the self-conductive network of the titanium carbide sheet rather than environmental humidity, which also makes the antistatic performance more stable. Moreover, the alkyl chain protects the surface of the titanium carbide sheet from oxidation or hydrolysis (especially in a humid and hot environment), maintaining long-term conductivity, and thus also improving the chemical stability of the spinning finish. In addition, the MXene sheet is stably dispersed in the spinning finish and is not easily aggregated due to mechanical shear or temperature changes, ensuring the durability of the conductive network.
[0016] In some embodiments, the spinning finish contains 40 - 55 wt% of a smoothing agent, and the smoothing agent is white oil.
[0017] In some embodiments, the spinning finish contains 15 - 19 wt% of an emulsifier, and the emulsifier is one or a combination of isotridecyl polyoxyethylene ether and sorbitan fatty acid ester.
[0018] In some embodiments, the spinning finish further contains 10 - 15 wt% of a wetting agent, and the wetting agent is fatty alcohol polyoxyethylene ether.
[0019] In some embodiments, the spinning finish further contains 7 - 10 wt% of a bundling agent, and the bundling agent is composed of a compound of polyethylene glycol 400 oleate and isotridecyl polyoxyethylene polyoxypropylene ether, specifically 3 - 5:1 - 1.5.
[0020] In some embodiments, the spinning finish further contains 3 - 5 wt% of an anti-coking agent, and the anti-coking agent is a fatty acid methyl ester ethoxylate double-capped surfactant.
[0021] In some embodiments, the water content in the spinning finish does not exceed 4 wt%.
[0022] In some embodiments, the total mass of each component in the spinning finish is 100 wt%.
[0023] In a second aspect, the present solution provides a method for preparing a highly stable antistatic crude oil-based spinning finish, comprising the following steps: While stirring and adding materials simultaneously, a smoothing agent, an emulsifier, an antistatic agent, a bundling agent, and a wetting agent are successively added into a reaction kettle. The antistatic agent includes alkyl-modified titanium carbide lamellae. The reaction temperature is set at 55-65 °C, the reaction rotation speed is 400-600 r / min, and the reaction time is 30-40 min.
[0024] For the content same as above in the embodiments of this preparation method, it will not be repeated here.
[0025] Compared with the prior art, the present technical solution has the following characteristics and beneficial effects: (1) The highly stable antistatic crude oil-based spinning finish of the present invention uses alkyl-modified titanium carbide lamellae as the core component of the antistatic agent, which can effectively avoid and reduce the problem that the commonly used phosphorus-based antistatic agent components containing salt are prone to coking at high temperatures.
[0026] (2) As a highly conductive lamellar material, alkyl-modified titanium carbide lamellae can greatly improve the conductivity of the spinning finish and effectively reduce the total dosage of the antistatic agent components.
[0027] (3) The antistatic agent used in the spinning finish of the present invention can significantly improve the stability of the antistatic performance of the spinning finish, making its antistatic performance not easily fluctuate due to environmental influence. Specific Embodiments
[0028] The technical solutions in the embodiments of the present invention will be clearly and completely described below. Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all of them. All other embodiments obtained by those of ordinary skill in the art based on the embodiments of the present invention belong to the scope protected by the present invention.
[0029] The following are the performance test methods in each embodiment: Conductivity (10% aqueous solution): Water is added to the spinning finish prepared in each of the following embodiments, and the mass of water accounts for 10% of the total solution, and it is measured according to GB / T 11007.
[0030] Oil film strength: A four-ball friction tester is used to measure the oil film strength of the sample to be tested with reference to GB / T 3142-1982 "Method for Determining the Load-Carrying Capacity of Lubricants (Four-Ball Method)".
[0031] Surface tension (1% aqueous solution): It is measured at 25 °C with a QBZY type platinum plate surface tension meter (QBZY-1 type, Shanghai Fangrui Instrument Co., Ltd.).
[0032] Fiber specific resistance: Measured by an automatic digital fiber specific resistance meter according to GB / T 14342-2015.
[0033] Fiber friction coefficient: Measured by a LFY-110 yarn dynamic friction tester (Model LFY-110, Shandong Textile Science Research Institute).
[0034] Oil content: Measured by a fiber oil rapid extractor (Model YG981, Changzhou Shuanggu Dunda Electromechanical Technology Co., Ltd.) according to the national standard GB / T6504-2008.
[0035] The following are the manufacturers and grades of the raw materials involved in the examples: Sodium dodecyl sulfate: Manufacturer is Aladdin Reagent (Shanghai) Co., Ltd., grade is 151-21-3.
[0036] Sodium dodecyl sulfonate: Manufacturer is Aladdin Reagent (Shanghai) Co., Ltd., grade is 2386-53-0.
[0037] Alkyl-capped lamellar Mxene: Self-made.
[0038] White oil (liquid paraffin): Manufacturer is Shanghai Macklin Biochemical Co., Ltd., grade is 8042-47-5.
[0039] Polyethylene glycol 400 oleate: Manufacturer is Aladdin Reagent (Shanghai) Co., Ltd., grade is 9004-96-0.
[0040] Isotridecyl polyoxyethylene ether: Manufacturer is Aladdin Reagent (Shanghai) Co., Ltd., grade is 61827-42-7; Isotridecyl polyoxyethylene polyoxypropylene ether: Manufacturer is Guangdong Wengjiang Chemical Reagent Co., Ltd.; grade is 78330-23-1 Fatty alcohol polyoxyethylene ether: Manufacturer is Aladdin Reagent (Shanghai) Co., Ltd., grade is 68131-39-5 Sorbitan fatty acid ester: Manufacturer is Nantong Ningyuan New Materials Technology Co., Ltd.; Fatty acid methyl ester ethoxylate double-capped surfactant: Manufacturer is Aladdin Reagent (Shanghai) Co., Ltd., grade is 65218-33-7.
[0041] Example 1: A preparation method of a highly stable antistatic crude oil type spinning oil agent, the specific steps are as follows: (1) Preparation of raw materials; Antistatic agent: A mixture of alkyl-capped lamellar Mxene, sodium dodecyl sulfate and sodium dodecyl sulfonate with a mass ratio of 1:1:1; Smoothing agent: White oil; Emulsifier: isoceteth; Wetting agent: laureth; Anti-coking agent: fatty acid methyl ester ethoxylate double-capped surfactant; Water; (2) Prepare the bundling agent; Mix polyethylene glycol 400 oleate and isoceteth oxypropylene ether at a mass ratio of 3:1 to obtain the bundling agent; (3) Weigh 7 wt% of the antistatic agent, 50 wt% of the leveling agent, 17 wt% of the emulsifier, 12 wt% of the wetting agent, 8 wt% of the bundling agent, 4 wt% of the anti-coking agent, and 2 wt% of water in proportion. Then, while stirring, add the leveling agent, emulsifier, antistatic agent, bundling agent, wetting agent, and water in sequence. React for 35 min at a temperature of 60 °C and a stirring speed of 550 r / min to obtain the high-performance spinning finish.
[0042] The finally obtained high-performance spinning finish is yellow and transparent, with a conductivity of 1279 μS / cm, an oil film strength of 1048.6 N, and a surface tension of 32.38 mN / m.
[0043] During the spinning process, the splashing of the finish is minimal, and there is almost no coking deposit.
[0044] The finally obtained polyester FDY fiber has a fiber specification of 70 dtex / 48f, a fiber specific resistance of 8.9×10 6 Ω·cm, a fiber friction coefficient of 0.3785, and an oil content of 0.67%.
[0045] Comparative Example 1: A preparation method of a highly stable antistatic crude oil-based spinning finish is basically the same as that of Example 1, except that the antistatic agent is sodium dodecyl sulfate.
[0046] The finally obtained high-performance spinning finish is yellow and transparent, with a conductivity of 717.3 μS / cm, an oil film strength of 862.4 N, and a surface tension of 33.79 mN / m.
[0047] During the spinning process, the splashing of the finish is less, and there is less coking deposit.
[0048] The finally obtained polyester FDY fiber has a fiber specification of 68 dtex / 48f, a fiber specific resistance of 8.4×10 7 Ω·cm, a fiber friction coefficient of 0.4017, and an oil content of 0.47%.
[0049] Comparative Example 2: A preparation method of a highly stable antistatic crude oil-based spinning finish is basically the same as that of Comparative Example 1, except that the antistatic agent is sodium dodecyl sulfate and sodium dodecyl sulfonate.
[0050] The finally prepared high-performance spinning finish presents a yellow transparent state, with a conductivity of 745.2 μS / cm, an oil film strength of 803.6 N, and a surface tension of 33.41 mN / m.
[0051] During the spinning process, there is less splashing of the finish and fewer coking deposits.
[0052] The finally prepared polyester FDY fiber has a fiber specification of 68 dtex / 48 f, a fiber specific resistance of 6.9×10 7 Ω·cm, a fiber friction coefficient of 0.4002, and an oil content of 0.48%.
[0053] Comparative Example 3: A preparation method of a highly stable antistatic crude oil-based spinning finish is basically the same as that of Comparative Example 1, except that the antistatic agent is sodium dodecyl sulfonate.
[0054] The finally prepared high-performance spinning finish presents a yellow transparent state, with a conductivity of 807.3 μS / cm, an oil film strength of 921.2 N, and a surface tension of 33.71 mN / m.
[0055] During the spinning process, there is less splashing of the finish and fewer coking deposits.
[0056] The finally prepared polyester FDY fiber has a fiber specification of 68 dtex / 48 f, a fiber specific resistance of 5.1×10 7 Ω·cm, a fiber friction coefficient of 0.3912, and an oil content of 0.58%.
[0057] Example 2: A preparation method of a highly stable antistatic crude oil-based spinning finish is as follows: (1) Preparation of raw materials; Antistatic agent: A mixture of alkyl-capped lamellar Mxene and sodium dodecyl sulfate with a mass ratio of 1:1; Smoothing agent: White oil; Emulsifier: Sorbitan fatty acid ester; Wetting agent: Fatty alcohol polyoxyethylene ether; Anti-coking agent: A fatty acid methyl ester ethoxylate-based double-capped surfactant; Water; (2) Preparation of the bundling agent; Prepare a bundling agent by mixing polyethylene glycol 400 oleate and isoceteth-10 in a mass ratio of 5:1.5. (3)Weigh 6 wt% of antistatic agent, 55 wt% of leveling agent, 15 wt% of emulsifier, 10 wt% of wetting agent, 7 wt% of bundling agent, 3 wt% of anti-coking agent, and 4 wt% of water in proportion. Then, add the leveling agent, emulsifier, antistatic agent, bundling agent, wetting agent, and water in sequence while stirring. React for 30 min at a temperature of 55 °C and a stirring speed of 400 r / min to obtain a high-performance spinning finish. The finally obtained high-performance spinning finish is yellow and transparent, with a conductivity of 1123.7 μS / cm, an oil film strength of 921.2 N, and a surface tension of 32.54 mN / m.
[0058] During the spinning process, there is no splashing of the finish and no coking deposits.
[0059] The finally obtained polyester FDY fiber has a fiber specification of 69 dtex / 48 f, a fiber specific resistance of 3.5×10 7 Ω·cm, a fiber friction coefficient of 0.3882, and an oil content of 0.64%.
[0060] Example 3: A preparation method of a highly stable antistatic crude oil-based spinning finish, the specific steps are as follows: (1)Preparation of raw materials; Antistatic agent: A mixture of alkyl-capped lamellar Mxene and sodium dodecyl sulfonate with a mass ratio of 1:1; Leveling agent: White oil; Emulsifier: A mixture of isoceteth-3 and sorbitan fatty acid ester with a mass ratio of 1:1; Wetting agent: Alcohol polyoxyethylene ether; Anti-coking agent: Fatty acid methyl ester ethoxylate double-capped surfactant; Water; (2)Prepare the bundling agent; Prepare a bundling agent by mixing polyethylene glycol 400 oleate and isoceteth-10 in a mass ratio of 4:1.25. (3) Weigh 8 wt% of antistatic agent, 40 wt% of smoothing agent, 19 wt% of emulsifier, 15 wt% of wetting agent, 10 wt% of bundling agent, 5 wt% of anti-coking agent, and 3 wt% of water in proportion. Then, while stirring, add the smoothing agent, emulsifier, antistatic agent, bundling agent, wetting agent, and water in sequence. React for 40 min at a temperature of 65 °C and a stirring speed of 600 r / min to obtain a high-performance spinning finish. The finally obtained high-performance spinning finish is in a yellow transparent state, with a conductivity of 1069.1 μS / cm, an oil film strength of 980 N, and a surface tension of 32.76 mN / m.
[0061] During the spinning process, there is no splashing of the finish and no coking deposits.
[0062] The finally obtained polyester FDY fiber has a fiber specification of 70 dtex / 48 f, a fiber specific resistance of 4.7×10 7 Ω·cm, a fiber friction coefficient of 0.368, and an oil content of 0.51%.
[0063] The above-described embodiments are only used to illustrate the present invention and not to limit the scope of the present invention. In addition, it should be understood that after reading the content taught by the present invention, those skilled in the art can make various changes or modifications to the present invention, and these equivalent forms belong to the protection scope of the present invention.
[0064] Those skilled in the art should understand that the technical features of the above embodiments can be combined arbitrarily. For the sake of brevity of description, not all possible combinations of the technical features in the above embodiments are described. However, as long as the combinations of these technical features do not conflict, they should all be considered as within the scope described in this specification.
[0065] The above embodiments only represent several implementation manners of the present application. Their descriptions are relatively specific and detailed, but they should not be construed as limiting the scope of the present application. It should be noted that for those of ordinary skill in the art, without departing from the concept of the present application, several modifications and improvements can still be made, and these all belong to the protection scope of the present application. Therefore, the protection scope of the present application should be subject to the appended claims.
Claims
1. A highly stable antistatic crude oil-based spinning finish, characterized in that, Including: A smoothing agent, an emulsifier, an antistatic agent, a bundling agent, and a wetting agent, wherein the antistatic agent includes alkyl-modified titanium carbide lamellae.
2. The high-stability antistatic crude oil-based spinning finish according to claim 1, wherein The antistatic agent additionally includes one or a combination of sodium dodecyl sulfate and sodium dodecyl sulfonate.
3. The highly stable antistatic crude oil-based spinning finish according to claim 1, characterized in that, The mass content of the antistatic agent is 6-8 wt%.
4. The highly stable antistatic crude oil-based spinning finish according to claim 1, wherein The alkyl-modified titanium carbide lamellae are titanium carbide lamellae with alkylation modification on the surface, and the alkyl-modified titanium carbide lamellae have a two-dimensional lamellar structure.
5. The high-stability antistatic crude oil-based spinning finish according to claim 4, characterized in that, The preparation method of the alkyl-modified titanium carbide lamellae is as follows: S1: Prepare a titanium carbide slurry; Add LiF to the HCl solution and stir well in an ice bath to obtain a mixed solution. Slowly pour Ti3AlC2 into the mixed solution and react at 35 °C to 40 °C for 12 to 48 h to obtain an acidic solution. Repeatedly centrifuge and wash the acidic solution with deionized water until the pH of the supernatant is about 6 to 6.5, and exfoliate Ti3C2Tx nanosheets through the oscillation operation during centrifugation. x nanosheets; S2: Alkyl-modify the titanium carbide lamellae: Centrifuge and replace the water solvent of the Ti3C2Tx sheets with acetone to prepare a dispersion, and ultrasonically treat the dispersion under an inert atmosphere to obtain a monolayer of Ti3C2T x acetone suspension. Add octyltriethoxysilane to the acetone suspension of monolayer Ti3C2T x and stir at room temperature for 6 - 96 h. After centrifugally washing the unreacted octyltriethoxysilane with acetone, alkyl-modified titanium carbide sheets are obtained.
6. The high-stability antistatic crude oil-based spinning finish according to claim 1, characterized in that, The spinning finish contains 40-55 wt% of the smoothing agent, 15-19 wt% of the emulsifier, 10-15 wt% of the wetting agent, and 7-10 wt% of the bundling agent.
7. The highly stable antistatic crude oil-based spinning finish according to claim 1, characterized in that, The water content in the spinning finish does not exceed 4 wt%.
8. The highly stable antistatic crude oil-based spinning finish according to claim 1, characterized in that, The smoothing agent is white oil, the emulsifier is one or a combination of isotridecyl polyoxyethylene ether and sorbitan fatty acid ester, the wetting agent is fatty alcohol polyoxyethylene ether, and the bundling agent is composed of a compound of polyethylene glycol 400 oleate and isotridecyl polyoxyethylene polyoxypropylene ether.
9. The high-stability antistatic crude oil-based spinning finish according to claim 1, characterized in that, The spinning finish also contains 10-15 wt% of the wetting agent, and the wetting agent is fatty alcohol polyoxyethylene ether.
10. A preparation method of a highly stable antistatic crude oil-based spinning finish, characterized in that, Including the following steps: In a reaction kettle, add the smoothing agent, emulsifier, antistatic agent, bundling agent, and wetting agent in a manner of adding materials while stirring. The antistatic agent includes alkyl-modified titanium carbide lamellae. Set the reaction temperature to 55-65 °C, the reaction rotation speed to 400-600 r / min; the reaction time is 30-40 min.
Citation Information
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