KR20130027690A - Manufacturing method of carbon nanofiber strand - Google Patents

Abstract

PURPOSE: A producing method of a carbon nanofiber strand is provided to enable users to use a conventional kneader for producing conjugate yarns from nanofiber tape yarns. CONSTITUTION: A producing method of a carbon nanofiber strand comprises the following steps: dissolving a carbon fiber precursor polymer material in a solvent, and electrospinning the mixture to obtain a spinning solution; spinning the spinning solution to obtain a polymer nanofiber web with the average diameter smaller than 1 micrometer; laminating the polymer nanofiber web to obtain a polymer membrane; slitting the polymer membrane to obtain nanofiber tape yarns; weaving and twining the nanofiber tape yarns to obtain the strand containing nanofibers; oxidation-stabilizing the strand to obtain the strand formed with thermosetting property nanofibers; carbonizing the strand in the inert atmosphe to obtain the carbon nanofiber strand; and graphitizing the carbon nanofiber strand. [Reference numerals] (AA) Spinning solution; (BB) Nanofiber web; (CC) Nanofiber laminating; (DD) Nanofiber tape yarns; (EE) Nanofiber strands; (FF) Oxidization stabilized strands; (GG) Carbon(graphite) nanofiber strands

Description

Manufacturing Method of Carbon Nanofiber Strand

The present invention relates to a method for producing carbon nanofiber strands, and specifically, after laminating nanofibers obtained by electrospinning carbon fiber precursor polymers, slitting at a predetermined interval, and then weaving and twisting (twisting). The present invention relates to a method for producing carbon nanofiber strands through oxidation stabilization and carbonization.

Nanofiber refers to a thin, flexible material having a diameter of less than 1 μm and a length / diameter (L / D) of 100 or more, and is used for drawing, self-assembling, and chemical vapor deposition. It can be manufactured in various ways by techniques such as -deposition, phase-separation and electrospinning. Among them, electrospinning is known to be the most effective method in terms of process convenience, mass production, and application of final products.

Electrospinning was already described in US Patent No. 1,975,504 to A. Formhals in 1934, but since then practical applications have been rarely reported except for some filter applications. The reason is that the electrospinning method has low fiber productivity and the micrometer-sized melt-blown spinning or flash spinning meets the needs of the times than nanoscale fibers. Recently, however, as nanotechnology has begun to attract attention, research on electrospinning has been exploding in terms of mass production, commercialization, and commercialization since the 2000s.

Electrospinning applies a high-voltage electric field to a polymer solution to form a nano-sized fibrous material with a diameter of less than 1 μm (hereinafter referred to simply as “nanofiber”) as a web or a three-dimensional nonwoven fabric. woven fabric). The nanofibers produced are filter materials for air and water purification, medical adhesion agents, dressing materials, wiping cloths, artificial leather or clothing, and carbon nanofibers for energy storage, and organic / inorganic mixed spinning. It is used for the purpose of inorganic nanofibers etc.

However, the nonwoven fabric composed of nanofibers forms a web in the form of short fibers, and the molecular orientation of the fiber itself is not achieved, so that its own strength is weaker than that of filament fiber yarn, and its handleability is low. There is a limit to application in high value-added high-tech applications such as super fiber.

Therefore, if manufactured in the form of filament, yarn, or strand using nanofibers, the physical properties can be dramatically improved, and various secondary workpieces such as weaving and knitting can be manufactured. The use of the fibers can be greatly expanded.

In general, carbon fiber refers to a fibrous material having a carbon content of 90% or more, and melt-spinning, solution spinning, or melt-blown spinning the carbon fiber precursor material. To produce thermoplastic organic fibers through a series of processes such as oxidation stabilization, carbonization, and graphitization, and carbon nanotubes or vapor-grown carbon fibers. As described above, the hydrocarbon gas may be classified by a method of producing the pyrolyzed hydrocarbon gas.

Among these methods, a method for obtaining filaments, yarns, or strands composed of carbon fibers includes oxidative stabilization and subsequent carbonization and graphitization of organic fibers produced by melt spinning, solution spinning, or melt spinning, which are conventional fiber manufacturing methods. It has been used in various industries by manufacturing high performance carbon fiber (HPCF) and general carbon fiber (general performance carbon fiber, GPCF). However, the carbon fiber produced by such a method has a problem that the diameter of the fiber is about several micrometers to several tens of micrometers, so that the excellent physical properties and functions of the nanofibers cannot be realized.

As a technique for obtaining carbon nanofibers from electrospun nanofibers, Korean Patent Application No. 10-2005-0004575 "Preparation of Activated Carbon Fibers with Nanopore Distribution by Carbonization of Nanofibers Prepared by Electrospinning Method Method ", No. 10-2005-0037214" Method for producing electrode catalyst for fuel cell using nanocomposite carbon fiber support "and No. 10-2006-0097815" Method for oxidation stabilization of nanofiber and nonwoven fabric for carbon fiber production " It has been proposed by the inventor of the application.

However, the conventional methods are carbon nanofibers obtained by carbonizing an electrospun nanofiber web after oxidation stabilization with a web itself, and stabilization and carbonized web are composed of short fibers so that they may be broken even in a weak impact. It is difficult to produce carbon nanofiber strands by slitting after stabilization or slitting after carbonization. Accordingly, it is difficult to secure mechanical properties to the extent that secondary processing such as weaving and knitting are possible, and there is a problem to be solved from the viewpoint of mass production and handling.

Particularly, in order to obtain high-performance carbon fiber, heat treatment should be performed under a certain tension in order to achieve molecular orientation in the carbonization and graphitization process after oxidation stabilization. There was a limit to imparting tension.

KR 10-2009-0103931 KR 10-2005-0004575 KR 10-2005-0037214 KR 10-2006-0097815

Therefore, the present invention has been proposed to solve the above-mentioned conventional problems, and the object of the present invention is a simple manufacturing process, excellent weaving and knitting, and good physical properties such as elongation, which can be used for various purposes. It is to provide a method for producing a fiber strand.

In addition, another object of the present invention is to further expand the use of nanofibers by suggesting a new method for producing carbon nanofiber strands.

According to the present invention for achieving the above object,

(a) dissolving a carbon fiber precursor polymer material in a solvent to prepare a spinning solution after electrospinning;

(b) spinning the spinning solution by a spinning method to obtain a polymer nanofiber web composed of an average diameter of less than 1 μm;

(c) laminating the nanofiber web to obtain a polymer membrane;

(d) slitting the polymer membrane to obtain nanofiber tape yarns;

(e) plying and twisting the nanofiber tape yarns to obtain strands comprising nanofibers;

(f) oxidatively stabilizing the strand to obtain a strand composed of thermosetting nanofibers:

(g) carbonizing the oxidatively stabilized strands in an inert atmosphere to obtain carbon nanofiber strands; And

(h) there is provided a method for producing carbon nanofiber strands comprising the step of graphitizing the obtained carbon nanofiber strands.

In the present invention, the strand (strand) is a fibrous material obtained through S, Z bitumen, coalescence, and is not particularly divided into filament such as filament or spun yarn such as yarn, and refers to filaments, yarns, or strands composed of nanofibers. I use it to mean.

In the present invention, the carbon fiber is used to refer to a fiber manufactured through carbonization, graphitization, and activation process having a carbon content of 90% or more.

Hereinafter, the manufacturing method of the carbon nanofiber strand of this invention is demonstrated in detail.

First, the carbon fiber precursor polymer material is dissolved in a suitable solvent to make a concentration capable of spinning, and then, using an electrospinning apparatus, nanofibers having a diameter of less than 1 μm are prepared to have a basis weight of 0.1-100 gsm (gram per square meter). . Here, basis weight is defined as the radiation amount per unit area of the polymer.

Carbon fiber precursor polymers usable in the present invention include, for example, polyacrylnitrile (PAN), pitch, cellulose derivatives, polyvinylidene fluoride (PVDF), Polyimide (PI), polyaramid (polyaramid), phenol-based resin (phenol-based resin) and the like can be composed of a combination of two or more kinds, carbon fiber precursor that can be produced in a fibrous form by electrospinning Any polymer can be a thermoplastic or thermoset polymer. Therefore, the polymer that can be used in the present invention is not particularly limited to the above-described polymer material.

In addition, in the present invention, various nanoparticles may be added to the spinning solution to improve the physical properties of the final product and to modify the treatment. For example, carbon black, carbon nanotubes, and graphene ), Alumina, silica, TiO ₂ inorganic particles and metal nanoparticles and the like can be dispersed in the spinning solution to perform electrospinning. The nanoparticles usable in the present invention are not particularly limited to the above materials.

Solvents usable in the present invention are dimethyl formamide (di-methylformamide, DMF), dimethyl acetamide (di-methylacetamide, DMAc), THF (tetrahydrofuran), acetone, alcohol (Alcohol), chloroform (Chloroform) , DMSO (dimethyl sulfoxide), dichloromethane (dichloromethane), acetic acid (acetic acid), formic acid (formic acid), NMP (N-Methylpyrrolidone), characterized in that at least one selected from the group consisting of alcohols, and water.

Meanwhile, the spinning methods usable in the present invention include electrospinning, electrospray, electro-blown spinning, centrifugal electrospinning, flash-electrospinning, and And nozzleless electrospinning.

At this time, when the basis weight of the polymer used is less than 0.1gsm, the handleability is inferior and the slitting process tends to be unstable, and when it exceeds 100gsm, there is a problem that the cost of the subsequent laminating process is increased. There is a disadvantage that the composite yarn is thick.

The laminating of the nanofiber web is preferably performed by at least one of pressurization, calendering, heat treatment, rolling, thermal bonding, and ultrasonic bonding. In the present invention, a material obtained by laminating, that is, a laminated web is defined as a membrane.

Subsequently, the polymer membrane is slitted to prepare a nanofiber tape yarn. Nanofiber tape yarn can be manufactured by various methods such as cutting and slitting, and when slitting the width of the nanofiber tape yarn to less than 0.1mm, it is difficult to cut smoothly, and the probability of trimming occurs when tension and twist is applied. In addition, when slitting the width of the nanofiber tape yarn more than 30mm, there is a high probability that the twist is uneven during the twisting step, there is a disadvantage that the final product is thick. Therefore, it is preferable that the nanofiber tape yarn having a basis weight of 0.1 to 100 gsm and a width of 0.1 to 30 mm.

Plywood and twist the nanofiber tape yarns to obtain strands comprising nanofibers. In this step, the tension can be given as necessary within the range that is not trimmed, and specifically, can be spun in a state in which a tension or less than 1 kg of tension is applied. If the tension exceeds 1kg, it may cause the trimming during twisting and weaving.

As a method of imparting tension to the nanofiber tape yarns, the nanofiber tape yarns can be stretched by passing the nanofiber tape yarns between the up disk tensioner and the down disk tensioner. In addition, the weaving can be carried out after winding the tensioning tape yarn screening and tension-provided nanofiber tape yarn in a separate bobbin, and after weaving the nanofiber tape yarn by equalizing the tension of the screening and tape yarn It may also go through a continuous burst.

In the twisting step, by twisting in the S or Z direction using a twisting machine, it is possible to manufacture multiple composite yarns such as two-ply and three-ply yarns. It is a process of manufacturing a nanofiber coated yarn.

The oxidation stabilization step is a process of changing a structure to maintain a fibrous structure in the subsequent high temperature carbonization heat treatment process by converting the thermoplastic material into a thermosetting material by heat-treating the strand composed of nanofibers in air or oxidizing gas atmosphere. At this time, the heat treatment temperature is carried out in the range of 240 ℃ to 350 ℃, if carried out in the range of less than 240 ℃ oxygen introduction process is insufficient to melt in the carbonization process to obtain carbon fiber, and if it exceeds 350 ℃ partially melt And there is a disadvantage that the final carbonization yield is lowered by excessive oxygen introduction. At this time, the temperature increase rate during the heat treatment is preferably carried out in the range of 0.1 to 5 ℃ per minute so that oxygen can be sufficiently introduced. If the temperature increase rate is less than 0.1 ℃, the process cost increases, the final carbonization yield may be lowered due to excessive oxygen introduction, and when the temperature exceeds 5 ℃, the introduction of oxygen on the nanofiber strand is uneven or insufficient, so that carbon fibers cannot be obtained smoothly. Cases may occur. In particular, it is preferable to adjust the nanofiber strand to induce stretching between the nanofibers and induce molecular orientation in the nanofibers so that finally high-strength carbon fibers can be obtained.

The carbonization step is a step of obtaining a carbon nanofiber strand consisting of carbon atoms by releasing atoms other than carbon to the outside of the nanofiber by subjecting the oxide stabilized nanofiber strand to high temperature heat treatment. The heat treatment at this time is preferably carried out in an inert gas or vacuum atmosphere such as nitrogen (N ₂ ) or argon (Ar) in the range of 500 ℃ to 1500 ℃. In this case as well, it is possible to uniformly induce alignment between the carbon molecules in the finally obtained carbon fiber by applying tension as necessary.

The graphitization step is a step of rearranging the carbon structure in the carbon nanofiber by heat-treating the carbonized heat-treated carbon nanofiber strand in the temperature range of 1500 ℃ to 3000 ℃, this graphitization step is a high-performance carbon such as high strength yarn or high elastic yarn This is a particularly required process for preparing fibers. In this case, a tension may be provided to induce a uniform distribution of carbon molecules in the carbon fiber.

Meanwhile, according to the present invention, the activation process may be performed on the carbon nanofiber strands in which the oxidation stabilization or carbonization process is completed. Specifically, the activation treatment is heat-treated in the temperature range of 600 ℃ to 1000 ℃ using carbon nanofiber strands, such as steam or inorganic salts such as KOH, ZnCl ₂ , H ₃ PO ₄ by imparting pores on the surface of the nanofibers It is a process to maximize the specific surface area of nanofibers.

This activation treatment is carried out as necessary when used for the purpose of water treatment and activated carbon fibers for atmospheric purification, electrode material for electric double layer supercapacitor, various catalyst carriers, etc., and fine pores are applied to the surface of the carbon fibers by such activation treatment. do. When the activating treatment is required, it is preferable to use steam or a chemical activating agent in the range of 600 to 1000 ° C. which is the reaction temperature of the chemical activating agent. It is usually not carried out after the graphitization step.

Since the carbon nanofiber strands prepared by the present invention include nanofibers, they may exceed the critical performance not seen in the existing carbon fibers, and because of the excellent physical properties of high strength and high elasticity, excellent weaving and knitting can be expected. Fabrics composed of carbon nanofibers, can be usefully used in the production of knitted fabrics.

In addition, according to the present invention, since the nanofiber tape yarn obtained by slitting the nanofiber web can be manufactured as a composite yarn using a conventional twisting machine, ready-made equipment can be used as it is, as well as reducing manufacturing costs, handling, and mass production. Stability and uniformity are further improved.

In addition, the strand composed of carbon nanofibers can be applied to various applications in many industries.

1 is a flow chart showing a method for producing a carbon nanofiber strand consisting of nanofibers according to the present invention,
2 is a graph showing a scanning electron micrograph (a) and a diameter distribution of a PAN nanofiber web prepared according to the present invention;
Figure 3 is a digital image photograph (a) of the nanofiber tape yarn manufactured by the present invention and a scanning electron micrograph (b) of the nanofiber cut to a slitting width 1.5mm,
Figure 4 is a photograph of the image of the nanofiber strands synthesized 1, 2, and 3 synthesized according to the present invention,
Figure 5a is a scanning electron micrograph of the magnification of the nanofiber strand single-bonded by the present invention, Figures 5b and 5c are scanning electron micrographs of the nanofiber strand double- and three-ply synthesized by the present invention,
6 is a scanning electron micrograph (a) and an AFM image (b) of a carbon nanofiber strand carbonized by the present invention, and a scanning electron micrograph (c) and an AFM image (d) of a graphitized carbon nanofiber. ),
FIG. 7 is an image photograph of a nanofiber web containing carbon nanotubes prepared according to the present invention. (A) 100% PAN (MWCNT not contained), (b) 5% MWCNT, and (c) 10% MWCNT. Photos,
8 is a scanning electron micrograph of carbon nanofibers containing 5% carbon nanotubes according to the present invention, (a) is a surface photograph, and (b) shows an image of carbon nanotubes composited in PAN fibers.

In the method for producing a carbon nanofiber strand according to the present invention, first, the carbon fiber precursor material is dissolved in an appropriate solvent to prepare a solution at a spinnable concentration, and transferred to a spinneret so that a high voltage is applied to the nozzle so that the basis weight is 0.1 to 100 gsm. Electrospinning, laminating it, and then slitting it to a width of 0.1 to 30 mm to obtain a tape yarn composed of a carbon fiber precursor.

The nanofiber tape yarns thus obtained are plied and twisted together with nanofiber tape yarns or screening to produce strands composed of nanofibers. The nanofiber strand is subjected to oxidative stabilization in an oxidizing atmosphere, and carbonized or graphitized in an inert atmosphere to produce carbon nanofiber strands.

Figure 1 shows the overall process flow chart of the carbon nanofiber strand manufacturing method according to the present invention.

Hereinafter, each process will be described in detail with reference to FIG. 1.

Preparation of spinning solution

A spinning solution is prepared by dissolving the precursor polymer for carbon fiber at a spinnable concentration using a suitable solvent. In the present invention, the polymer material may include polyacrylnitrile (PAN), pitch, cellulose derivatives, polyvinylidene fluoride (PVDF), polyimide (PI), and the like. The polyaramid, phenol-based resin, or the like, is not particularly limited as long as the polymer is formed by nanospinning alone or in combination by electrospinning. In addition, it is possible to spin by dispersing nanoparticles and the like in the spinning solution.

When preparing the spinning solution, the content of the high molecular material is about 5 to 50% by weight, and less than 5% by weight is difficult to form a membrane by spraying onto beads rather than forming nanofibers, and more than 50% by weight. In the case of, the viscosity of the spinning solution is so high that it is difficult to form fibers due to poor spinning properties. Therefore, it is preferable to control the morphology of the fiber to prepare the spinning solution at a concentration that is easy to form a fibrous structure.

Formation of Polymer Nanofiber Webs

The spinning solution is transferred to a spin pack using a metering pump, and the electrospinning is performed by applying a voltage to the spinning pack using a high voltage regulator. At this time, the voltage used can be adjusted from 0.5kV to 100kV, the current collector may be grounded or charged to the (-) pole and is preferably composed of an electrically conductive metal, release paper, and the like. In the case of the current collector plate, it is preferable to use a suction collector attached to smooth the concentration of fibers during spinning.

In addition, the distance between the spin pack and the current collector is preferably adjusted to 5 ~ 50 cm. The amount of discharge during spinning is uniformly discharged using a metering pump to spin, and it is preferable to spin in an environment with a relative humidity of 30-80% in a chamber that can control temperature and humidity during spinning.

Laminating of Polymer Nanofiber Webs

The prepared polymer nanofiber web is laminated by various methods such as pressing, rolling, thermal bonding, and ultrasonic bonding to prepare a polymer membrane to have a basis weight of 0.1 to 100 gsm. In the present invention, the laminating may be referred to as a step of film-forming the nanofiber spinning web by pressing and fixing by a method such as heat treatment or ultrasonic wave so that the individual fibers are not moved alone.

If the basis weight is less than 0.1 gsm, there is a high probability of defects in handling or slitting, and if it exceeds 100 gsm, the manufacturing cost increases, so the basis weight is 0.1-100 gsm.

In addition, laminating may be carried out with a heat treatment, it is preferable to perform in a temperature range of 20 ~ 250 ℃ that the polymer used is not melted. If the temperature is less than 20 ℃, the fusion between nanofibers is unstable because the heat treatment temperature is too low, or the polymer with high glass transition temperature hardly occurs between the nanofibers. . In addition, since the polymer constituting the nanofibers melts when the heat treatment temperature exceeds 250 ° C., the fibrous structure is likely to be lost, which is not preferable. At this time, it is also possible to use a method of stretching using heat treatment or the like.

Preparation of Nanofiber Tapes

The laminated nanofiber polymer membrane is slitted to a width of 0.1 to 30 mm by various methods using a cutter or slitter to prepare a tape yarn composed of nanofibers. When the width of the nanofiber tape yarn is to be less than 0.1mm, the width is too small, making it difficult to cut smoothly using slitter, as well as increasing the probability of trimming when applying tension and twist. In addition, if the width of the slitting more than 30mm, there is a high probability of uneven twisting in the twisting stage. Therefore, it is preferable that the nanofiber tape yarn has a basis weight of 0.1 to 100 gsm and a width of 0.1 to 30 mm.

Preparation of Nanofiber Strands

At the plying and twisting stages, it is advisable to ply the nanofiber tape yarns with tensioned tensioning and tensioning so that the screening does not protrude to the outside. It is preferable to use the same slitting nanofiber tape yarn as the screening. For example, when using existing nylon or PET as the screening, the screening is melted or decomposed in the stabilization and subsequent high temperature carbonization or graphitization processes to obtain normal carbon nanofibers.

In addition, the nanofiber tape yarn may be plied with the screening in a state where a tension of 1 kg or less is applied. If the tension exceeds 1kg, it may cause trimming during weaving.

As a method of imparting tension to the nanofiber tape yarns, the tension can be imparted by passing the nanofiber tape yarns between the up disk tensioner and the down disk tensioner.

In addition, the yarn can be subjected to the twisting step after winding the screening of the tension and the nanofiber tape yarn given a tension of 1kg or less in a separate bobbin, and after weaving each of the nanofiber tape yarn given tension continuously You can also go through the continuous shooting step.

Oxidation stabilization stage

Oxidation stabilization step is a process of changing the structure to maintain the fibrous structure in the subsequent high temperature carbonization process by converting the thermoplastic material into a thermosetting material by heat-treating the strand composed of nanofibers in air or oxidizing gas atmosphere. At this time, the heat treatment temperature is carried out in the range of 240 ℃ to 350 ℃, if carried out in the range of less than 240 ℃ oxygen introduction process is insufficient to melt during the carbonization process to obtain carbon fiber, and if it exceeds 350 ℃ partial melting And there is a disadvantage that the final carbonization yield is lowered by excessive oxygen introduction. At this time, the temperature increase rate during the heat treatment is preferably carried out in the range of 0.1 to 5 ℃ per minute so that oxygen can be sufficiently introduced. If the temperature increase rate is less than 0.1 ℃, the process cost increases, and the final carbonization yield may be lowered by excessive oxygen introduction, and when the temperature exceeds 5 ℃, the introduction of oxygen on the nanofiber strand is unstable or insufficient, so that carbon fibers can be smoothly obtained. There will be no. At this time, it is preferable to adjust the strands to induce stretching between the nanofibers and induce molecular orientation in the nanofibers so as to be a final high-strength carbon fiber.

Carbonization, Graphitization and Activation Steps

The carbonization step is a step of obtaining a fiber composed of carbon atoms by releasing non-carbon atoms to the outside of the nanofiber by subjecting the oxidatively stabilized strand to high temperature heat treatment. At this time, the heat treatment temperature is preferably performed in the range of 500 ° C to 1500 ° C, preferably inert gas of nitrogen or argon or in a vacuum atmosphere. At this time, the tension can be given to uniformly induce the arrangement between the carbon molecules in the final carbon fiber.

In the graphitization step, the carbonized sample may be heat-treated at a temperature in the range of 1500 ° C. to 3000 ° C. and a tension may be applied to induce uniform distribution of graphite molecules in the carbon fiber.

In addition, the activation step is heat-treated in the temperature range of 600 ℃ to 1000 ℃ using steam or inorganic salts, such as KOH, ZnCl ₂ , H ₃ PO ₄ by oxidation-stabilized or carbonized strands to give pores to the surface of the nanofibers To maximize the specific surface area, which is carried out as necessary.

Hereinafter, the present invention will be described in more detail with reference to Examples. However, the examples are only for illustrating the present invention and the scope of the present invention should not be limited by these examples.

(Example 1)

1. Preparation of PAN Nanofiber Tapes

A spinning solution was prepared by dissolving PAN (polyacrylonitrile) of Mitsui Chemical Co. Ltd. having a molecular weight of 400,000 in 20 wt% of a solvent DMAc. The spinning solution was transferred to a spinning nozzle using a metering pump, and spinning was performed under an applied voltage of 25 kV, a distance of 20 cm between the spinneret and the current collector, a spinning temperature of 30 ° C., and a relative humidity of 60% normal pressure to obtain a PAN nanofiber web. .

Figure 2 shows a scanning electron micrograph (a) and a graph of the diameter distribution of the nanofibers (b) of the PAN nanofiber spinning web obtained according to the present embodiment, respectively, confirming that the average diameter is made of about 350nm nanofibers Can be.

The basis weight of the nanofiber spinning web was about 10 gsm, and a lamination was carried out at a pressure of 100 g / cm ² using a roller heated at 100 ° C to the nanofiber spinning web to prepare a PAN membrane having a thickness of about 30 μm. , Slitting was performed to a width of 1.5mm using a slitter to obtain a PAN nanofiber tape yarn.

3 shows a digital image photograph (a) and a scanning electron micrograph (b) of PAN nanofiber tapes obtained by slitting according to the present embodiment.

2. Preparation of Nanofiber Strands Composed of PAN Nanofibers

Subsequently, the PAN nanofiber tape yarn obtained as described above was S-burned at a firing rate of 500 rpm using a twisting machine to obtain a strand composed of nanofibers. In addition, Z-twisted PAN nanofiber tape yarns were prepared on Z-bonded nanofibers, and two-ply yarns were prepared. At this time, the nanofibers wound in the bobbin did not occur trimming.

Figure 4 shows an image of a strand consisting of a single yarn, two yarns, and three-plyed nanofibers as described above, Figure 5a is a single plywood, Figure 5b is a two-plyed yarn, Figure 5c is a three-plyed PAN nanofibers Scanning electron micrographs are respectively shown.

3. Oxidative Stabilization, Carbonation and Graphitization of Nanofiber Strands

The PAN nanofiber strand was heated in an air atmosphere at 1 ° C. per minute and heat-treated at 300 ° C. for 60 minutes to obtain an oxide stabilized nanofiber strand. At this time, the orientation of the PAN molecules was induced by giving a tension such that the nanofibers were not cut during the oxidation stabilization process.

The oxidation stabilized nanofibers were subjected to carbonization heat treatment for 1 hour in a nitrogen gas atmosphere at 1000 ° C. to obtain carbon nanofiber strands. Next, graphitization was performed at the temperature of 3000 degreeC using the graphite resistance furnace of a vacuum atmosphere.

FIG. 6 is a scanning electron micrograph (a) and an AFM image (b) of a carbon nanofiber strand carbonized at 1000 ° C. according to the present invention, and a scanning electron micrograph of graphitized carbon nanofiber at 3000 ° C. c) and AFM image (d).

From the results of FIG. 6, it can be seen that when the graphitization treatment is performed after the carbonization treatment, the graphite crystals in the carbon fibers are rearranged and densified, and the carbon fibers exhibit a diameter reduction of about 40%. It can be seen that high strength and high elastic carbon fibers can be obtained.

5A to 5C and FIG. 6 show carbon nanofiber strands composed of PAN nanofibers only. That is, FIGS. 5A to 5C and 6 illustrate an example of configuring a composite yarn using only nanofiber tape yarns of the same type.

(Example 2)

Multi-walled carbon nanotubes (MWCNT) were added to commercially available PAN polymers having a molecular weight of 400,000 at 0, 5, and 10% by weight of PAN, and electrospinning was performed in the same manner as in Example 1. Strands were prepared and subjected to oxidation stabilization, carbonization, and graphitization.

7 is an image photograph of the nanofiber web containing the carbon nanotubes prepared according to the present embodiment (a) is 100% PAN, that is, the state does not contain MWCNT, (b) is 5% MWCNT containing State, and (c) represents the state containing 10% MWCNT. FIG. 8 is a scanning electron micrograph of carbon nanofibers containing 5% carbon nanotubes according to the present embodiment, (a) is a surface photograph, and (b) shows an image of carbon nanotubes composited in PAN fibers. .

7 and 8, it can be seen that the carbon nanofibers in which the nanoparticles are uniformly dispersed can be prepared by complexing carbon nanotubes and the like during electrospinning according to the present invention, and thus, carbon in the carbon nanofibers The complexation of nanotubes suggests that mechanical and thermal and electrical properties can be improved.

As described above, although the present invention has been described by way of limited embodiments and drawings, the present invention is not limited thereto, and the technical idea of the present invention and the following by those skilled in the art to which the present invention pertains. Of course, various modifications and variations are possible within the equivalent scope of the claims to be described.

Claims (12)

(a) dissolving a carbon fiber precursor polymer material in a solvent to prepare a spinning solution after electrospinning;
(b) spinning the spinning solution by a spinning method to obtain a polymer nanofiber web composed of an average diameter of less than 1 μm;
(c) laminating the nanofiber web to obtain a polymer membrane;
(d) slitting the polymer membrane to obtain nanofiber tape yarns;
(e) plying and twisting the nanofiber tape yarns to obtain strands comprising nanofibers;
(f) oxidatively stabilizing the strand to obtain a strand composed of thermosetting nanofibers:
(g) carbonizing the oxidatively stabilized strands in an inert atmosphere to obtain carbon nanofiber strands; And
(h) a method for producing carbon nanofiber strands comprising the step of graphitizing the obtained carbon nanofiber strands. The method of claim 1,
The carbon fiber precursor polymer material is a method for producing carbon nanofiber strands, characterized in that at least one selected from a polymer comprising PAN, cellulose derivatives, pitch, phenol, aramid, and imide. The method of claim 1,
And at least one selected from the group consisting of carbon nanotubes, graphite powder, carbon black, graphene powder, ceramics, and metal nanoparticles in the carbon fiber precursor polymer material. The method of claim 1,
The method of producing a carbon nanofiber strand, characterized in that the basis weight of the nanofibers obtained in the step (b) is 0.1 ~ 100gsm. The method of claim 1,
The nanofiber tape yarn width is 0.1 ~ 30mm manufacturing method of carbon nanofiber strands, characterized in that. The method of claim 1,
The laminating method of producing carbon nanofiber strands, characterized in that carried out in a temperature range of 20 ~ 250 ℃. The method of claim 1,
The method of manufacturing carbon nanofiber strands, characterized in that the weaving and twisting yarn weaving and twisting the nanofiber tape yarns of at least one homogeneous or heterogeneous carbon fiber precursor polymer material. The method of claim 1,
The method of manufacturing carbon nanofiber strands, characterized in that the weaving and twisting yarns weaving and twisting the screen with the nanofiber tape yarns to single or double covering. 8. The method of claim 7,
The method of manufacturing carbon nanofiber strands, characterized in that the yarns and twisted yarns give a tension of less than 1kg to the nanofiber tape yarns when the nanofiber tape yarns and the screening yarns. The method of claim 1,
The oxidation stabilization process in the step (f) is a method for producing carbon nanofiber strands, characterized in that carried out at 350 ℃ at a temperature increase rate of 0.1 to 5 ℃ per minute. The method of claim 1,
The carbonization process of the step (g) is a carbon nanofiber strand manufacturing method, characterized in that carried out in an inert gas or vacuum atmosphere of 500 ℃ to 1500 ℃ range. The method of claim 1,
The graphitization process of step (h) is a method for producing carbon nanofiber strands, characterized in that carried out in a vacuum atmosphere of 1500 ℃ to 3000 ℃ using a graphitization furnace.

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