US20170044689A1 - Carbon nanotube fiber and method for producing the same - Google Patents

Carbon nanotube fiber and method for producing the same Download PDF

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Publication number
US20170044689A1
US20170044689A1 US15/304,192 US201415304192A US2017044689A1 US 20170044689 A1 US20170044689 A1 US 20170044689A1 US 201415304192 A US201415304192 A US 201415304192A US 2017044689 A1 US2017044689 A1 US 2017044689A1
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carbon nanotube
nanotube fiber
cross
carbon
linking agent
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US15/304,192
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Kun-Hong Lee
Jaegeun LEE
A Lum JUNG
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Academy Industry Foundation of POSTECH
Posco Holdings Inc
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Posco Co Ltd
Academy Industry Foundation of POSTECH
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Assigned to POSCO, POSTECH ACADEMY-INDUSTRY FOUNDATION reassignment POSCO ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: JUNG, A Lum, LEE, JAEGEUN, LEE, KUN-HONG
Publication of US20170044689A1 publication Critical patent/US20170044689A1/en
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    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
    • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
    • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
    • D01F9/127—Carbon filaments; Apparatus specially adapted for the manufacture thereof by thermal decomposition of hydrocarbon gases or vapours or other carbon-containing compounds in the form of gas or vapour, e.g. carbon monoxide, alcohols
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00—Carbon; Compounds thereof
    • C01B32/15—Nano-sized carbon materials
    • C01B32/158—Carbon nanotubes
    • C01B32/16—Preparation
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D10/00—Physical treatment of artificial filaments or the like during manufacture, i.e. during a continuous production process before the filaments have been collected
    • D01D10/02—Heat treatment
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
    • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
    • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
    • D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
    • D01F9/20—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products
    • D01F9/21—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00—Manufacture or treatment of nanostructures
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/192—Polycarboxylic acids; Anhydrides, halides or salts thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/40—Fibres of carbon
    • D—TEXTILES; PAPER
    • D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2101/00—Inorganic fibres
    • D10B2101/10—Inorganic fibres based on non-oxides other than metals
    • D10B2101/12—Carbon; Pitch
    • D10B2101/122—Nanocarbons

Definitions

  • the present invention relates to carbon nanotube fiber and a method for producing the same.
  • a carbon nanotube is a nanomaterial having excellent mechanical strength, and tensile strength of one strand of the carbon nanotube is up to 150 GPa.
  • tensile strength of a carbon nanotube fiber is generally 2 GPa or less, which is very weak compared to the carbon nanotube.
  • the carbon nanotube fiber is consisting of many carbon nanotubes, but walls of the carbon nanotubes are not connected due to a van Der Waals force, which is weak molecule bonding.
  • a solvent may be sprayed to the carbon nanotube fiber or the carbon nanotube fiber may be soaked in the solvent so as to shrink the carbon nanotube fiber.
  • a distance between the carbon nanotube fibers is decreased such that the van Der Waals force can be enhanced, thereby increasing strength of the carbon nanotube fiber.
  • the fiber is soaked in a reaction solution and then a chemical reaction is performed thereon.
  • a reactant cannot be dispersed on the center of the carbon nanotube fiber so that the reaction can hardly occur in the center of the carbon nanotube. Accordingly, a desired effect cannot be acquired from the chemical reaction, and mechanical strength of the carbon nanotube fiber cannot be significantly enhanced.
  • the carbon nanotubes composing the carbon nanotube fiber have higher reactivity at end portions than in wall surfaces. Substantially, the cross-linking which has been reported up to now shows than the reaction mostly occurs in the end portions rather than in the wall surfaces of the carbon nanotubes, and thus bonding force between walls of the carbon nanotubes cannot be significantly increased.
  • tensile strength of the carbon nanotube fiber is increased to about 5 GPa.
  • the present invention has been made in an effort to provide an excellent carbon nanotube fiber having a tensile strength which exceeds 5 GPa.
  • Another exemplary embodiment of the present invention can provide a method for producing high-strength carbon nanotube fiber of which wall surfaces of carbon nanotubes are cross-linked.
  • carbon nanotube fiber having a tensile strength which exceeds 5 GPa can be provided.
  • Wall surfaces of carbon nanotubes that compose the carbon nanotube fiber may be cross-linked.
  • the cross-linking may be resulted from an acylation reaction between the wall surfaces of the carbon nanotubes.
  • the acylation reaction may be a one step reaction.
  • a diameter of a carbon nanotube may be 1 ⁇ m to 150 ⁇ m, and specifically, may be 3 ⁇ m to 30 ⁇ m.
  • a method for producing a high-strength carbon nanotube fiber precursor includes: producing a carbon nanotube fiber precursor consisting of carbon nanotubes; evenly dispersing a cross-linking agent on the carbon nanotube fiber precursor; and acquiring carbon nanotube fiber by thermally treating the carbon nanotube fiber precursor on which the cross-linking agent is evenly dispersed, wherein the acquired carbon nanotube fiber has cross-linking between wall surfaces of the carbon nanotubes each other.
  • the producing of a carbon nanotube fiber precursor consisting of the carbon nanotubes is performed by one of methods of forest spinning, direct spinning, and solution spinning. Specifically, the producing of a carbon nanotube fiber precursor consisting of the carbon nanotubes may be performed by forest spinning.
  • the producing of a carbon nanotube fiber precursor consisting of the carbon nanotubes may include: preparing a substrate; growing carbon nanotubes on the substrate; and drawing out carbon nanotube fiber from the substrate where the carbon nanotubes have been grown.
  • the substrate may include silicon.
  • the drawing out of the carbon nanotube fiber precursor from the substrate where the carbon nanotubes have been grown may be performed by stretching the carbon nanotubes grown on the substrate in one direction, and pulling out the stretched carbon nanotubes in the form of a noddle.
  • the carbon nanotube fiber precursor may be formed in the shape of a carbon nanotube ribbon.
  • the producing of a carbon nanotube fiber precursor consisting of the carbon nanotubes may be performed in a temperature range of 600° C. to 1000° C. Specifically, the temperature range may be 630° C. to 670° C.
  • At least one selected from a group of C1 to C20 hydrocarbons may be used as a carbon source.
  • the evenly dispersing of the cross-linking agent on the carbon nanotube fiber precursor may be performed by using one of an air gun, a nebulizer, heating, and vacuuming
  • the evenly dispersing of the cross-linking agent on the carbon nanotube fiber precursor may be performed by soaking one end of the carbon nanotube fiber precursor in the cross-linking agent in a liquid state.
  • the cross-linking agent may include two or more acyl groups. Specifically, the cross-linking agent may be one or more selected from a group including a halogenated acyl compound and a carboxylic acid compound. More specifically, the cross-linking agent may be one or more selected from a group including azelaic acid dichloride, poly(acryloyl chloride), azelaic acid, and polyacryl acid.
  • the acquiring of the carbon nanotube fiber by thermally treating the carbon nanotube fiber precursor on which the cross-linking agent is evenly dispersed may be performed through a one step reaction. Specifically, the acquiring of the carbon nanotube fiber by thermally treating the carbon nanotube fiber precursor on which the cross-linking agent is evenly dispersed may be performed through an acylation reaction.
  • the acquiring of the carbon nanotube fiber by thermally treating the carbon nanotube fiber precursor on which the cross-linking agent is evenly dispersed may be performed under a nitrogen or inert atmosphere.
  • the thermal treatment may be performed in a temperature range of 160° C. to 250° C.
  • a diameter of the acquired carbon nanotube fiber may be 1 ⁇ m to 150 ⁇ m.
  • Tensile strength of the acquired carbon nanotube fiber may be 5 GPa to 40 GPa, or specifically, may be 30 GPa to 40 GPa.
  • the tensile strength of the carbon nanotube fiber can be enhanced.
  • a simplified method for producing high-strength carbon nanotube fiber according to the present invention can be provided.
  • FIG. 1 is an analysis result of Fourier transformed infrared spectroscopy of carbon nanotube fiber according to an exemplary embodiment of the present invention (upper curve) and carbon nanotube fiber produced using a conventional method (lower curve).
  • FIG. 3 is a measurement result of tensile strength of the carbon nanotube fiber according to the exemplary embodiment of the present invention performed four times.
  • FIG. 4 is a measurement result of tensile strength of carbon nanotube fiber produced using a conventional method.
  • a carbon nanotube fiber having tensile strength which exceeds 5 GPa is provided.
  • the tensile strength may exceed 10 GPa, and specifically, may exceed 20 GPa, and more specifically may exceed 30 GPa.
  • the tensile strength is as high as possible for a desired effect, but in general, the tensile strength can be achieved to 36 GPa.
  • FIG. 2 is a scanning electron microscope of carbon nanotube fiber according to an exemplary embodiment of the present invention.
  • the carbon nanotube fiber may have a shape such that walls of the carbon nanotube fiber, which composes the carbon nanotube fiber, are combined in a crosslinked manner.
  • the cross-linking implies that carbon chains are chemically connected to each other directly or through several bonds at locations other than ends of the carbon chains. Since a covalent bond, which is stronger than van Der Waals force, is formed by the cross-linking, strength of the carbon nanotube can be increased.
  • cross-linking between walls rather than at ends of the carbon nanotubes can effectively increase shearing strength between carbon nanotubes. Accordingly, strength can be effectively transferred within the carbon nanotube fiber so that strength of the carbon nanotube fiber can be reinforced.
  • the cross-linking may be formed through an acylation reaction between walls of the carbon nanotubes.
  • the acylation reaction is a reaction that can substitute hydrogen included in an organic compound with an acyl group, and has higher reactivity in the wall of the carbon nanotube than in the end of the carbon nanotube.
  • the acylation reaction may be a one step reaction.
  • the crosslink can be formed through a simple process without undergoing several steps such as surface modification of the carbon nanotube and the like.
  • the diameter of the carbon nanotube fiber may be 1 ⁇ m to 150 ⁇ m, and particularly, 3 ⁇ m to 30 ⁇ m.
  • a method for producing high-strength carbon nanotube fiber includes: producing a carbon nanotube fiber precursor consisting of carbon nanotubes; evenly distributing a cross-linking agent in the carbon nanotube fiber precursor; and acquiring carbon nanotubes by thermally treating the carbon nanotube fiber precursor on which the cross-linking agent is evenly distributed, and the acquired carbon nanotube fiber is formed by cross-linking walls of the carbon nanotubes.
  • the carbon nanotube fiber precursor implies fiber that is formed by agglomerating carbon nanotubes which compose the carbon nanotube fiber precursor in an axis direction, and specifically, covers all of carbon nanotube ribbon, fiber, and yarn.
  • the carbon nanotube fiber precursor has a structure in which the carbon nanotubes are arranged in the axis direction, and specifically, is defined as a concept that covers carbon nanotube ribbons having a structure in which carbon nanotubes are arranged in a film shape, carbon nanotube fibers having a structure in which carbon nanotubes are arranged in the form of fiber, and carbon nanotube yarn having a structure in which carbon nanotubes are twisted.
  • the acquired carbon nanotube fiber is defined as carbon nanotube fibers having a structure in which walls of carbon nanotubes are cross-linked, That is, the acquired carbon nanotube differs from the carbon nanotube fiber precursor depending on whether or not the walls of the carbon nanotubes are cross-linked.
  • the producing of the carbon nanotube fiber precursor consisting of the carbon nanotubes may be performed by using one of forest spinning, direct spinning, and solution spinning, and specifically, the forest spinning may be used.
  • the forest spinning is a method in which a carbon nanotube forest is is composed on a substrate and then the carbon nanotube precursor is drawn out
  • the direct spinning is a method in which a carbon nanotube fiber is produced by composing the carbon nanotube in an aerogel state
  • the solution spinning is a method in which only carbon nanotubes are collected from a solution in which the carbon nanotubes are dispersed.
  • the forest spinning may include preparing a substrate, growing carbon nanotubes on the substrate, and drawing out a carbon nanotube precursor from the substrate where the carbon nanotubes have been grown.
  • the substrate is one of which the surface has very low roughness, and may include a silicon substrate or a silicon/silicon oxide substrate. Specifically, one or more selected from a group that includes alumina and iron may be deposited on the substrate. More specifically, a silicon oxide, alumina, and iron may be sequentially deposited on the silicon substrate.
  • the carbon nanotubes grown on the substrate may be stretched in one direction and then pulled out in the form of a noodle.
  • the carbon nanotube fiber precursor may have a shape of a carbon nanotube ribbon.
  • the carbon nanotube ribbon may be pulled out in the form of a noddle while pulling ends of vertically grown carbon nanotube arrays to a silicon wafer.
  • several nanometers of carbon nanotube bundles can be formed by collecting the carbon nanotubes, and the bundles of carbon nanotubes are collected such that a carbon nanotube ribbon having a very wide surface area can be formed.
  • the producing of the carbon nanotube precursor consisting of carbon nanotubes may be performed in a temperature range of 600° C. to 1000° C.
  • the temperature range exceeds 1000° C.
  • speed of dissolution of acetylene gas becomes too fast and thus carbon is excessively supplied such that a catalyst is poisoned, thereby deteriorating stable growth of the carbon nanotubes.
  • the temperature range is 600° C. or less, carbon is insufficiently supplied to the catalyst due to poor dissolution of acetylene gas.
  • the temperature range may specifically be 630° C. to 670° C.
  • the carbon nanotube precursor consisting of the carbon nanotubes is produced, at least one selected from a group of C1 to C20 hydrocarbons may be used as a carbon source, and specifically, one of acetylene, methane, and ethylene may be used.
  • one of an air gun, a nebulizer, heating, and vacuuming may be used.
  • the cross-linking agent is sprayed to the surface of the carbon nanotube fiber precursor, which has a maximum surface area, using the air gun, such that the cross-linking agent can be evenly dispersed within the carbon nanotube fiber precursor.
  • an end of the carbon nanotube fiber precursor is soaked in the cross-linking agent in a solution state. Then, the cross-linking agent can be evenly dispersed within carbon nanotube precursor by capillary action.
  • the cross-linking agent may include two or more acyl groups, and specifically, may be a material including acyl groups at opposite ends thereof.
  • cross-linking between walls of the carbon nanotubes that form the carbon nanotube fiber may be formed through a one step reaction.
  • the cross-linking agent is a material having very high reactivity, and may be one or more selected from a group including a halogenated acyl compound and a carboxylic acid compound.
  • azelaic acid dichloride that exists in a liquid state at room temperature may be used.
  • functional groups are included in opposite ends, cross-linking can be formed through a one step reaction.
  • the cross-linking agent may be one or more selected from a group including azelaic acid dichloride, poly(acryloyl chloride), azelaic acid, and polyacrylic acid.
  • the thermal treatment of the carbon nanotube fiber precursor on which the cross-linking agent is evenly dispersed and the acquiring the carbon nanotube fiber may be performed through the one step reaction. More specifically, they may be performed through an acylation reaction.
  • the cross-linking and the acylation reaction are as described above.
  • they may be performed under a nitrogen or inert atmosphere.
  • the heat treatment may be performed within a temperature range of 160° C. to 250° C.
  • the temperature range exceeds 250° C.
  • the cross-linking agent is dissolved such that cross-linking cannot occur, and when the temperature range is below 160° C., energy is not sufficient for causing a reaction.
  • a diameter of the acquired carbon nanotube fiber may be 1 ⁇ m to 150 ⁇ m, and specifically, may be 3 ⁇ m to 30 ⁇ m.
  • tensile strength of the acquired carbon nanotube fiber may be 5 GPa to 40 GPa.
  • the tensile strength of the acquired carbon nanotube fiber may be 20 GPa to 40 GPa, and more specifically, it may be 30 GPa to 40 GPa.
  • a carbon nanotube ribbon was formed on a substrate using forest spinning.
  • a silicon wafer (Siltron Inc. Korea, ⁇ 100> direction, thickness: 660-690 ⁇ m) where 300 nm of silicon dioxide (SiO 2 ) was deposited was used, 10 nm of aluminum oxide (Al 2 O 3 ) was deposited on the substrate using an atomic layer deposition method, and then 1 nm of iron (Fe) was deposited on the aluminum oxide using an e-beam deposition method.
  • the substrate was located at a center of a tube-type furnace (Lindberg Blue M, HTF55322, tube diameter 4 cm, length 70 cm), and then the temperature of the furnace was increased while injecting argon (Ar) at 500 sccm therein. After the temperature reached 670° C., which is a reaction temperature, a carbon nanotube array was composed by injecting argon at 386 sccm, hydrogen at 96 sccm, and acetylene at 19 sccm for about 3 min.
  • argon Ar
  • azelaic acid dichloride exists in a liquid state at room temperature, the azelaic acid dichloride could be evenly sprayed between carbon nanotubes in the carbon nanotube ribbon of which the surface area was maximized by using the air gun.
  • the carbon nanotube ribbon on which azelaic acid dichloride was evenly dispersed was placed in a furnace (Lindberg Blue M, HTF55322, tube diameter 4 cm, length 70 cm) and then heated to 160° C. under an argon atmosphere.
  • azelaic acid dichloride since azelaic acid dichloride has very high reactivity, azelaic acid dichloride reacted with an aromatic ring of a wall of the carbon nanotubes, thereby causing an acylation reaction. Further, since functional groups were included in opposite ends of the azelaic acid dichloride, cross-linking could be formed through a one step reaction.
  • One end of 100 nm-length carbon nanotube fiber produced in the above-stated exemplary embodiment was fixed and the other was connected to a motor.
  • an angle formed by the bottom and the fiber was set to be 10° to 15°.
  • Carbon nanotube fiber was produced by twisting the ribbon while rotating the motor at 200 rpm to 2000 rpm.
  • FIG. 1 shows a result of the Fourier transformed infrared spectroscopy analysis of the carbon nanotube fiber according to the exemplary embodiment (upper curve) and the carbon nanotube fiber according to the comparative example (lower curve).
  • Morphology and diameter of the carbon nanotube fiber according to the exemplary embodiment were respectively evaluated using a scanning electron microscope (Hitachi, S4800).
  • FIG. 2 is a scanning electron microscope photograph of the carbon nanotube fiber according to the exemplary embodiment.
  • the carbon nanotube fiber was shrunk while bundles of carbon nanotubes were aligned in the axis direction, and it can be determined that a diameter was about 3 ⁇ m.
  • Tensile strengths of the carbon nanotube fibers according to the exemplary embodiment and the comparative example were respectively measured.
  • a nano-tensile testing device NANO Bionix, Agilent Technologies
  • an end of a 10 mm-length carbon nanotube fiber was fixed and strain of 0.0027/s was applied to measure tensile strength thereof.
  • FIG. 3 shows a result of four measurements of tensile strength of the carbon nanotube fiber according to the exemplary embodiment of the present invention
  • FIG, 4 shows a result of measurement of tensile strength of the carbon nanotube fiber according to the comparative example.
  • the carbon nanotube filer of the comparative example had tensile strength of 0.4 GPa.
  • the carbon nanotube fiber of the exemplary embodiment had tensile strength of up to 36 GPa.
  • the carbon nanotube fiber according to the exemplary embodiment of the present invention has higher tensile strength compared to an existing carbon nanotube fiber. This is because the wall surfaces of the carbon nanotubes that compose the carbon nanotube fiber are cross-linked by the acylation reaction such that shear strength between the carbon nanotubes can be enhanced.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Nanotechnology (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Inorganic Fibers (AREA)
  • Mechanical Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
US15/304,192 2014-04-17 2014-08-04 Carbon nanotube fiber and method for producing the same Abandoned US20170044689A1 (en)

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KR10-2014-0046277 2014-04-17
KR1020140046277A KR101615338B1 (ko) 2014-04-17 2014-04-17 탄소나노튜브 섬유 및 그 제조방법
PCT/KR2014/007177 WO2015160041A1 (ko) 2014-04-17 2014-08-04 탄소나노튜브 섬유 및 그 제조방법

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EP (1) EP3133190A4 (ko)
JP (1) JP6368797B2 (ko)
KR (1) KR101615338B1 (ko)
CN (1) CN106232879B (ko)
AU (1) AU2014391194B2 (ko)
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US10889918B2 (en) 2017-01-04 2021-01-12 Lg Chem, Ltd. Method for controlling strength of carbon nanotube fiber aggregate
US11136711B2 (en) 2017-02-03 2021-10-05 Lg Chem, Ltd. Method for preparing carbon nanotube fiber and carbon nanotube fiber prepared thereby
CN114644337A (zh) * 2022-03-11 2022-06-21 电子科技大学 一种等离子体诱导高效催化碳纳米管阵列的方法

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KR102002909B1 (ko) * 2015-12-16 2019-07-26 주식회사 엘지화학 인장 강도와 내열성이 향상된 카본 나노튜브 섬유 및 이의 제조 방법
KR102069411B1 (ko) * 2016-10-31 2020-01-22 주식회사 엘지화학 인장강도가 향상된 카본나노튜브 섬유 및 이의 제조방법
KR102113382B1 (ko) * 2017-07-28 2020-05-20 주식회사 엘지화학 강도가 향상된 탄소 나노튜브 섬유 집합체의 제조 방법
KR101900331B1 (ko) 2017-07-28 2018-09-20 주식회사 화인지오텍 다겹 보온커튼 및 그 제조방법
CN109455694B (zh) * 2018-12-10 2020-11-03 深圳烯湾科技有限公司 改性碳纳米管阵列、碳纳米管纤维及其制备方法和应用

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AU2014391194A1 (en) 2016-11-17
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