阅读说明：本技术 一种石墨烯抗病毒粘胶纤维及其制备方法 (Graphene antiviral viscose fiber and preparation method thereof ) 是由 沙嫣 沙晓林 马立国 于 2021-08-06 设计创作，主要内容包括：本发明公开了一种石墨烯抗病毒粘胶纤维及其制备方法,该方法包含：步骤1,按比例称取各原料；各原料包含粘胶浆粕,石墨烯,表面活性剂,碱性试剂,水；步骤2,制备石墨烯粉体；步骤3,将石墨烯粉体分散至水中,超声,配置成水溶液,然后加入表面活性剂及碱性试剂,将溶液调整至中性或弱碱性,再将其超声,得到石墨烯分散液；步骤4,制备纤维素浆粕,再将石墨烯分散液升温后,与浆粕充分混合,并进行搅拌；步骤5,采用纤维浆粕进行纺丝。本发明还提供了通过该方法制备的石墨烯抗病毒粘胶纤维。本发明制备的石墨烯粘胶复合纤维具备抗菌、抗病毒等功能,扩展粘胶纤维应用范围,是一种健康环保的复合纤维。(The invention discloses a graphene antiviral viscose fiber and a preparation method thereof, wherein the method comprises the following steps: step 1, weighing raw materials in proportion; each raw material comprises viscose pulp, graphene, a surfactant, an alkaline reagent and water; step 2, preparing graphene powder; step 3, dispersing graphene powder into water, performing ultrasonic treatment to prepare an aqueous solution, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and performing ultrasonic treatment to obtain a graphene dispersion solution; step 4, preparing cellulose pulp, heating the graphene dispersion liquid, fully mixing the graphene dispersion liquid with the pulp, and stirring; and 5, spinning by adopting fiber pulp. The invention also provides the graphene antiviral viscose fiber prepared by the method. The graphene viscose composite fiber prepared by the invention has antibacterial and antiviral functions, expands the application range of viscose fiber, and is a healthy and environment-friendly composite fiber.)

1. A preparation method of graphene antiviral viscose fiber is characterized by comprising the following steps:

step 1, weighing raw materials in proportion; each raw material comprises viscose pulp, graphene, a surfactant, an alkaline reagent and water;

step 2, preparing graphene powder;

step 3, dispersing graphene powder into water, performing ultrasonic treatment to prepare an aqueous solution, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and performing ultrasonic treatment to uniformly disperse the solution to obtain a graphene dispersion solution;

step 4, preparing cellulose pulp, namely firstly mixing the viscose pulp with a sodium hydroxide solution, and uniformly mixing the viscose pulp and the sodium hydroxide solution by stirring; then putting the pulp into a squeezer for squeezing, then carrying out aging treatment on the pulp, and yellowing after the aging is finished; heating the graphene dispersion liquid obtained in the step 3, fully mixing the graphene dispersion liquid with pulp, and stirring;

and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

2. The method for preparing graphene antiviral viscose fiber according to claim 1, wherein in the step 1, the amount of each raw material is 60 to 85 mass percent of viscose pulp, 0.1 to 10 mass percent of graphene, 0.1 to 5 mass percent of surfactant, 0.1 to 5 mass percent of alkaline agent, and the balance of water.

3. The method for preparing the graphene antiviral viscose fiber according to claim 2, wherein the surfactant is polyvinyl alcohol, polyvinylpyrrolidone and sodium dodecyl benzene sulfonate in a mass ratio of 1: (2-4): (3-6) mixing.

4. The method for preparing graphene antiviral viscose fiber according to claim 2, wherein the alkaline reagent is any one or more of ammonia water, potassium hydroxide and sodium hydroxide.

5. The method for preparing graphene antiviral viscose fiber according to claim 1, wherein in the step 2, the graphene powder is prepared by a chemical vapor deposition method.

6. The method for preparing graphene antiviral viscose fiber according to claim 5, wherein the step 2 comprises:

step 2.1, cutting the copper foil for growing the graphene into a size according to needs, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, then closing the vacuum pump, introducing hydrogen and argon with a volume flow ratio of 1: 2-3, wherein the introduction amount of the hydrogen is 200 plus 300mi/min, closing an air source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow rate of 1-5 ml/min, introducing 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene;

and 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

7. The method for preparing graphene antiviral viscose fiber according to claim 1, wherein in the step 2, the D90 of the obtained graphene powder is less than 1 μm.

8. The preparation method of the graphene antiviral viscose fiber according to claim 1, wherein in the step 3, the graphene powder is dispersed in deionized water, ultrasonic treatment is performed for 30-50 min to prepare an aqueous solution with a concentration of 10-50 mg/ml, then a surfactant and an alkaline reagent are added to adjust the solution to be neutral or weakly alkaline, and then ultrasonic treatment is performed for 10-30 min to uniformly disperse the solution, so that a graphene dispersion solution is obtained.

9. The preparation method of the graphene antiviral viscose fiber as claimed in claim 1, wherein in the step 4, 500-800g of viscose pulp is weighed, mixed with 20-40% sodium hydroxide solution by mass ratio of 1 (2-4), and stirred by a stirrer for 20-50 min to be completely mixed; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

10. a graphene antiviral viscose fiber prepared by the method of any one of claims 1 to 9.

Technical Field

The invention relates to a graphene composite antiviral fiber and a preparation method thereof, and particularly relates to a graphene antiviral viscose fiber and a preparation method thereof.

Background

Graphene is a single-layer carbon atom material stripped from graphite, and a single-layer two-dimensional honeycomb lattice structure is formed by tightly packing carbon atoms, and is known to be the material with the thinnest thickness, the hardest texture and the best conductivity. Graphene has excellent mechanical, optical and electrical properties and a very stable structure, researchers have not found that graphene has a missing carbon atom, the linkage between carbon atoms is very flexible, and is harder than diamond, the strength is 100 times higher than that of the world's best steel, if graphene is used for making a packaging bag, the graphene can bear about two tons of articles, the graphene is almost completely transparent, but is very compact, waterproof and airtight, helium gas with the minimum atomic size cannot pass through the graphene, the graphene has good conductivity, the movement speed of electrons in graphene reaches 1/300 of the light speed, the conductivity exceeds that of any traditional conductive material, the chemical properties are similar to the surface of graphite, various atoms and molecules can be adsorbed and desorbed, and the graphene also has the capability of resisting strong acid and strong alkali.

Viscose is a cellulose fiber with wide application, has good mechanical property and hygroscopicity, but does not have functionality. The traditional functional viscose fiber is mainly realized by adding an auxiliary agent into the viscose fiber or modifying the fiber, and the viscose fiber prepared by the method has the defects of poor water washing resistance and serious pollution caused by post-treatment, so that the application of the viscose fiber is limited to a certain extent.

Disclosure of Invention

The invention aims to provide a graphene composite fiber and a preparation method thereof, and the prepared graphene viscose composite fiber has antibacterial and antiviral functions, expands the application range of viscose fiber, and is a healthy and environment-friendly composite fiber.

In order to achieve the above object, the present invention provides a method for preparing graphene antiviral viscose fiber, wherein the method comprises: step 1, weighing raw materials in proportion; each raw material comprises viscose pulp, graphene, a surfactant, an alkaline reagent and water; step 2, preparing graphene powder; step 3, dispersing graphene powder into water, performing ultrasonic treatment to prepare an aqueous solution, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and performing ultrasonic treatment to uniformly disperse the solution to obtain a graphene dispersion solution; step 4, preparing cellulose pulp, namely firstly mixing the viscose pulp with a sodium hydroxide solution, and uniformly mixing the viscose pulp and the sodium hydroxide solution by stirring; then putting the pulp into a squeezer for squeezing, then carrying out aging treatment on the pulp, and yellowing after the aging is finished; heating the graphene dispersion liquid obtained in the step 3, fully mixing the graphene dispersion liquid with pulp, and stirring; and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

In the step 1, the raw materials include, by mass, 60-85% of viscose pulp, 0.1-10% of graphene, 0.1-5% of a surfactant, 0.1-5% of an alkaline reagent, and the balance water.

The preparation method of the graphene antiviral viscose fiber comprises the following steps of: (2-4): (3-6) mixing.

In the preparation method of the graphene antiviral viscose fiber, the alkaline reagent is any one or more of ammonia water, potassium hydroxide and sodium hydroxide.

In the preparation method of the graphene antiviral viscose fiber, in the step 2, the graphene powder is prepared by a chemical vapor deposition method.

The preparation method of the graphene antiviral viscose fiber comprises the following steps of: step 2.1, cutting the copper foil for growing the graphene into a size according to needs, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, then closing the vacuum pump, introducing hydrogen and argon with a volume flow ratio of 1: 2-3, wherein the introduction amount of the hydrogen is 200 plus 300mi/min, closing an air source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow rate of 1-5 ml/min, introducing 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene; and 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

In the preparation method of the graphene antiviral viscose fiber, in the step 2, D90 of the obtained graphene powder is less than 1 μm.

In the step 3, the graphene powder is dispersed in deionized water, ultrasonic treatment is carried out for 30-50 min to prepare a water solution with the concentration of 10-50 mg/ml, then a surfactant and an alkaline reagent are added to adjust the solution to be neutral or weakly alkaline, and ultrasonic treatment is carried out for 10-30 min to uniformly disperse the solution, so that the graphene dispersion liquid is obtained.

In the step 4, 500-800g of viscose pulp is weighed and mixed with 20-40% sodium hydroxide solution according to the mass ratio of 1 (2-4), and the mixture is stirred for 20-50 min by a stirrer to be completely mixed; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

the invention also provides the graphene antiviral viscose fiber prepared by the method.

The graphene antiviral viscose fiber and the preparation method thereof provided by the invention have the following advantages:

the invention develops the graphene antiviral viscose composite fiber, and the composite fiber has the outstanding characteristics of antibacterial and antiviral performances, is washing-resistant in functionality, does not need a separate post-treatment process, is safe and environment-friendly, and better meets the requirements of current people on functional, comfortable and healthy textiles.

The composite fiber prepared by the invention has excellent antibacterial and antiviral performances, wherein the antibacterial rate of escherichia coli, staphylococcus aureus and candida albicans reaches 99%, the antiviral effect of H1N1 is more than 90%, and the composite fiber has good functionality.

The graphene antiviral viscose composite fiber prepared by the method is simple in process, easy to operate, low in cost, high in economic benefit and suitable for large-scale industrial production.

Detailed Description

The following further describes embodiments of the present invention.

The invention provides a preparation method of graphene antiviral viscose fiber, which comprises the following steps:

step 1, weighing raw materials in proportion; each raw material comprises viscose pulp, graphene, a surfactant, an alkaline reagent and water; step 2, preparing graphene powder; step 3, dispersing graphene powder into water, performing ultrasonic treatment to prepare an aqueous solution, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and performing ultrasonic treatment to uniformly disperse the solution to obtain a graphene dispersion solution; step 4, preparing cellulose pulp, namely firstly mixing the viscose pulp with a sodium hydroxide solution, and uniformly mixing the viscose pulp and the sodium hydroxide solution by stirring; then putting the pulp into a squeezer for squeezing, then carrying out aging treatment on the pulp, and yellowing after the aging is finished; heating the graphene dispersion liquid obtained in the step 3, fully mixing the graphene dispersion liquid with pulp, and stirring; and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

Preferably, the raw materials in step 1 comprise, by mass, 60% to 85% of viscose pulp, 0.1% to 10% of graphene, 0.1% to 5% of surfactant, 0.1% to 5% of alkaline reagent, and the balance water.

The surfactant is polyvinyl alcohol, polyvinylpyrrolidone (PVP) and sodium dodecyl benzene sulfonate according to the mass ratio of 1: (2-4): (3-6) mixing.

The alkaline reagent is one or more of ammonia water, potassium hydroxide and sodium hydroxide.

In the step 2, the graphene powder is prepared by a chemical vapor deposition method.

The step 2 comprises the following steps: step 2.1, cutting the copper foil for growing the graphene into a size according to needs, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, then closing the vacuum pump, introducing hydrogen and argon with a volume flow ratio of 1: 2-3, wherein the introduction amount of the hydrogen is 200 plus 300mi/min, closing an air source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow rate of 1-5 ml/min, introducing 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene; and 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

In the step 2, D90 of the obtained graphene powder is less than 1 μm.

And 3, dispersing the graphene powder into deionized water, carrying out ultrasonic treatment for 30-50 min to prepare a water solution with the concentration of 10-50 mg/ml, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and carrying out ultrasonic treatment for 10-30 min to uniformly disperse the solution to obtain the graphene dispersion liquid.

In the step 4, 500-800g of viscose pulp is weighed and mixed with 20-40% of sodium hydroxide solution according to the mass ratio of 1 (2-4), and the mixture is stirred for 20-50 min by a stirrer to be completely mixed; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

the equipment and spinning process conditions parameters, etc. employed in the present invention are known to those skilled in the art.

The invention also provides the graphene antiviral viscose fiber prepared by the method.

The graphene antiviral viscose fiber and the preparation method thereof provided by the present invention are further described with reference to the following embodiments.

Example 1

A method for preparing graphene antiviral viscose fiber, comprising:

step 1, weighing raw materials in proportion; the raw materials comprise viscose pulp, graphene, a surfactant, an alkaline reagent and water.

Preferably, the raw materials comprise, by mass, 85% of the viscose pulp, 0.1% of graphene, 0.1% of a surfactant, 0.1% of an alkaline agent and the balance of water.

The surfactant is polyvinyl alcohol, polyvinylpyrrolidone and sodium dodecyl benzene sulfonate according to the mass ratio of 1: 2: 3, and mixing the two components.

The alkaline reagent is ammonia water.

And 2, preparing graphene powder.

The graphene powder is prepared by a chemical vapor deposition method.

The step 2 comprises the following steps:

step 2.1, cutting the copper foil for growing the graphene according to the required size, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, closing the vacuum pump, introducing hydrogen and argon with the volume flow ratio of 1: 2-3, introducing the hydrogen at 200 plus temperature of 300mi/min, closing a gas source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow of 1-5 ml/min, introducing the ethylene gas for 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene.

And 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

The D90 of the obtained graphene powder is less than 1 mu m.

And 3, dispersing the graphene powder into deionized water, carrying out ultrasonic treatment for 30-50 min to prepare a water solution with the concentration of 10-50 mg/ml, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and carrying out ultrasonic treatment for 10-30 min to uniformly disperse the solution to obtain the graphene dispersion liquid.

And 4, preparing cellulose pulp.

Weighing 500-800g of viscose pulp, mixing with 20-40% of sodium hydroxide solution according to the mass ratio of 1 (2-4), and stirring for 20-50 min by a stirrer to completely mix the solution; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

The embodiment also provides the graphene antiviral viscose fiber prepared by the method.

Example 2

A method for preparing graphene antiviral viscose fiber, comprising:

step 1, weighing raw materials in proportion; the raw materials comprise viscose pulp, graphene, a surfactant, an alkaline reagent and water.

Preferably, the raw materials comprise, by mass, 80% of viscose pulp, 2% of graphene, 1% of surfactant, 1% of alkaline agent and the balance of water.

The surfactant is polyvinyl alcohol, polyvinylpyrrolidone and sodium dodecyl benzene sulfonate according to the mass ratio of 1: 2.5: 4, and mixing.

The alkaline agent is potassium hydroxide.

And 2, preparing graphene powder.

The graphene powder is prepared by a chemical vapor deposition method.

The step 2 comprises the following steps:

step 2.1, cutting the copper foil for growing the graphene according to the required size, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, closing the vacuum pump, introducing hydrogen and argon with the volume flow ratio of 1: 2-3, introducing the hydrogen at 200 plus temperature of 300mi/min, closing a gas source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow of 1-5 ml/min, introducing the ethylene gas for 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene.

And 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

The D90 of the obtained graphene powder is less than 1 mu m.

And 3, dispersing the graphene powder into deionized water, carrying out ultrasonic treatment for 30-50 min to prepare a water solution with the concentration of 10-50 mg/ml, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and carrying out ultrasonic treatment for 10-30 min to uniformly disperse the solution to obtain the graphene dispersion liquid.

And 4, preparing cellulose pulp.

Weighing 500-800g of viscose pulp, mixing with 20-40% of sodium hydroxide solution according to the mass ratio of 1 (2-4), and stirring for 20-50 min by a stirrer to completely mix the solution; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

The embodiment also provides the graphene antiviral viscose fiber prepared by the method.

Example 3

A method for preparing graphene antiviral viscose fiber, comprising:

step 1, weighing raw materials in proportion; the raw materials comprise viscose pulp, graphene, a surfactant, an alkaline reagent and water.

Preferably, the raw materials comprise, by mass, 75% of the viscose pulp, 5% of graphene, 2% of a surfactant, 3% of an alkaline agent and the balance water.

The surfactant is polyvinyl alcohol, polyvinylpyrrolidone and sodium dodecyl benzene sulfonate according to the mass ratio of 1: 3: 4.5 mixing to obtain the product.

The alkaline agent is sodium hydroxide.

And 2, preparing graphene powder.

The graphene powder is prepared by a chemical vapor deposition method.

The step 2 comprises the following steps:

step 2.1, cutting the copper foil for growing the graphene according to the required size, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, closing the vacuum pump, introducing hydrogen and argon with the volume flow ratio of 1: 2-3, introducing the hydrogen at 200 plus temperature of 300mi/min, closing a gas source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow of 1-5 ml/min, introducing the ethylene gas for 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene.

And 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

The D90 of the obtained graphene powder is less than 1 mu m.

And 3, dispersing the graphene powder into deionized water, carrying out ultrasonic treatment for 30-50 min to prepare a water solution with the concentration of 10-50 mg/ml, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and carrying out ultrasonic treatment for 10-30 min to uniformly disperse the solution to obtain the graphene dispersion liquid.

And 4, preparing cellulose pulp.

Weighing 500-800g of viscose pulp, mixing with 20-40% of sodium hydroxide solution according to the mass ratio of 1 (2-4), and stirring for 20-50 min by a stirrer to completely mix the solution; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

The embodiment also provides the graphene antiviral viscose fiber prepared by the method.

Example 4

A method for preparing graphene antiviral viscose fiber, comprising:

step 1, weighing raw materials in proportion; the raw materials comprise viscose pulp, graphene, a surfactant, an alkaline reagent and water.

Preferably, the raw materials comprise, by mass, 65% of viscose pulp, 8% of graphene, 4% of a surfactant, 4% of an alkaline agent and the balance of water.

The surfactant is polyvinyl alcohol, polyvinylpyrrolidone and sodium dodecyl benzene sulfonate according to the mass ratio of 1: 3.5: 5, and mixing.

The alkaline reagent is any one of ammonia water, potassium hydroxide and sodium hydroxide.

And 2, preparing graphene powder.

The graphene powder is prepared by a chemical vapor deposition method.

The step 2 comprises the following steps:

step 2.1, cutting the copper foil for growing the graphene according to the required size, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, closing the vacuum pump, introducing hydrogen and argon with the volume flow ratio of 1: 2-3, introducing the hydrogen at 200 plus temperature of 300mi/min, closing a gas source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow of 1-5 ml/min, introducing the ethylene gas for 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene.

And 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

The D90 of the obtained graphene powder is less than 1 mu m.

And 3, dispersing the graphene powder into deionized water, carrying out ultrasonic treatment for 30-50 min to prepare a water solution with the concentration of 10-50 mg/ml, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and carrying out ultrasonic treatment for 10-30 min to uniformly disperse the solution to obtain the graphene dispersion liquid.

And 4, preparing cellulose pulp.

Weighing 500-800g of viscose pulp, mixing with 20-40% of sodium hydroxide solution according to the mass ratio of 1 (2-4), and stirring for 20-50 min by a stirrer to completely mix the solution; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

The embodiment also provides the graphene antiviral viscose fiber prepared by the method.

Example 5

A method for preparing graphene antiviral viscose fiber, comprising:

step 1, weighing raw materials in proportion; the raw materials comprise viscose pulp, graphene, a surfactant, an alkaline reagent and water.

Preferably, the raw materials comprise, by mass, 60% of viscose pulp, 10% of graphene, 5% of a surfactant, 5% of an alkaline agent and the balance of water.

The surfactant is polyvinyl alcohol, polyvinylpyrrolidone and sodium dodecyl benzene sulfonate according to the mass ratio of 1: 4: 6, and mixing.

The alkaline reagent is any of ammonia water, potassium hydroxide and sodium hydroxide.

And 2, preparing graphene powder.

The graphene powder is prepared by a chemical vapor deposition method.

The step 2 comprises the following steps:

step 2.1, cutting the copper foil for growing the graphene according to the required size, placing the copper foil into a quartz tube, vacuumizing the quartz tube through a vacuum pump, closing the vacuum pump, introducing hydrogen and argon with the volume flow ratio of 1: 2-3, introducing the hydrogen at 200 plus temperature of 300mi/min, closing a gas source after the quartz tube furnace reaches normal pressure, raising the temperature of the tube furnace to 800-1200 ℃, introducing ethylene gas with the flow of 1-5 ml/min, introducing the ethylene gas for 10-20 min, closing the ethylene gas source, cooling the tube furnace to room temperature, and taking out a copper foil sample deposited with the graphene.

And 2.2, placing the copper foil sample deposited with the graphene into a ferric chloride solution, treating for 1-3 h, after the copper foil is corroded, carrying out ultrasonic treatment on the solution to further strip the graphene, filtering to obtain the graphene, and drying to obtain graphene powder.

The D90 of the obtained graphene powder is less than 1 mu m.

And 3, dispersing the graphene powder into deionized water, carrying out ultrasonic treatment for 30-50 min to prepare a water solution with the concentration of 10-50 mg/ml, adding a surfactant and an alkaline reagent, adjusting the solution to be neutral or weakly alkaline, and carrying out ultrasonic treatment for 10-30 min to uniformly disperse the solution to obtain the graphene dispersion liquid.

And 4, preparing cellulose pulp.

Weighing 500-800g of viscose pulp, mixing with 20-40% of sodium hydroxide solution according to the mass ratio of 1 (2-4), and stirring for 20-50 min by a stirrer to completely mix the solution; then putting the mixture into a squeezer for squeezing, wherein the pressure is set to be 1-5 kpa, and the squeezing time is 30-60 min; then carrying out aging treatment on the pulp, wherein the aging temperature is 25-30 ℃, the aging time is 1-3 h, then heating the temperature to 30-35 ℃, and the aging time is 2-3 h; yellowing is carried out after the aging is finished, wherein the yellowing temperature is 22-27 ℃, and the yellowing time is 30-50 min; and then heating the graphene dispersion liquid prepared in the step 3 to 25-30 ℃, fully mixing the graphene dispersion liquid with pulp, and stirring the mixture by a stirrer for 20-50 min, wherein the solid content of the graphene and the solid content of the pulp cellulose are in a proportion of (0.01-5%): 1.

and 5, spinning by adopting the fiber pulp obtained in the step 4 to prepare the graphene antiviral viscose composite fiber.

The embodiment also provides the graphene antiviral viscose fiber prepared by the method.

The graphene antiviral viscose fibers obtained in the embodiments of the present invention are tested, and the results are shown in table 1 below.

TABLE 1 test results.

The invention discloses a graphene anti-virus viscose fiber and a preparation method thereof, and aims to prepare an anti-virus graphene viscose composite fiber by utilizing an improved graphene preparation and dispersion technology and an improved viscose preparation process. The invention introduces a graphene in the formula, so that the viscose composite fiber has the functions of antibiosis, antivirus and the like. The graphene prepared by the method is thinner and smaller in particle size, and according to the graphene antibacterial principle, the graphene is densely distributed in the fiber and on the surface, part of the graphene is embedded in the fiber, and part of the graphene is exposed out of the surface of the fiber, so that a graphene nano knife which is more beneficial to killing viruses is formed, the viruses are killed, and the aim of resisting viruses is fulfilled.

While the present invention has been described in detail with reference to the preferred embodiments, it should be understood that the above description should not be taken as limiting the invention. Various modifications and alterations to this invention will become apparent to those skilled in the art upon reading the foregoing description. Accordingly, the scope of the invention should be determined from the following claims.