This disclosure relates to the technical field of carbon nanotubes, provides an ultra-long chiral carbon nanotube and a method for preparing the same. The ultra-long chiral carbon nanotube has a diameter of about 1.5 nm to 5.5 nm and has a length of about 100 mm to 650 mm, the ultra-long chiral carbon nanotube includes a double-walled carbon nanotube and a triple-walled carbon nanotube, and each layer of the ultra-long chiral carbon nanotube is semiconducting and has a helix angle greater than 10°.

A carbon nanotube-resin composite includes: a carbon nanotube assembled wire including a plurality of carbon nanotubes; and a resin, wherein in the carbon nanotube assembled wire, the carbon nanotubes are oriented at a degree of orientation of 0.9 or more and 1 or less.

A method and a device for preparing a carbon nanotube and a prepared carbon nanotube. The method includes: adding iron pentcarbonyl and nickel tetracarbonyl into a multi-stage series fluidized bed and performing decomposition to obtain a catalyst, and discharging the carbon monoxide generated; adding a carbon source and injecting an inert gas into the series fluidized bed for reaction under heating at 600-800° C. for 40-90 min, the ratio of the mass of carbon in the carbon source to the mass of the catalyst being 5-7:3-5. Further provided are a device for preparing a carbon nanotube according to the above method and a carbon nanotube prepared by the above method.

A method and a device for preparing a carbon nanotube and a prepared carbon nanotube. The method includes: adding iron pentcarbonyl and nickel tetracarbonyl into a multi-stage series fluidized bed and performing decomposition to obtain a catalyst, and discharging the carbon monoxide generated; adding a carbon source and injecting an inert gas into the series fluidized bed for reaction under heating at 600-800° C. for 40-90 min, the ratio of the mass of carbon in the carbon source to the mass of the catalyst being 5-7:3-5. Further provided are a device for preparing a carbon nanotube according to the above method and a carbon nanotube prepared by the above method.

A production method for growing a carbon nanotube assembly on a substrate having a catalyst on a surface thereof. In this production method, in each of a formation unit that carries out a formation step of reducing a catalyst on the substrate and a growth unit that carries out a growth step of growing a carbon nanotube assembly, the substrate is continuously being conveyed using conveyance units that convey the substrate by screw rotations. In carrying out the formation step and the growth step, these steps are carried out while the gas environments in these steps are prevented from mixing with each other.

A production method for growing a carbon nanotube assembly on a substrate having a catalyst on a surface thereof. In this production method, in each of a formation unit that carries out a formation step of reducing a catalyst on the substrate and a growth unit that carries out a growth step of growing a carbon nanotube assembly, the substrate is continuously being conveyed using conveyance units that convey the substrate by screw rotations. In carrying out the formation step and the growth step, these steps are carried out while the gas environments in these steps are prevented from mixing with each other.

The present disclosure is directed to providing a carbon film having an excellent shield performance against electromagnetic waves. The carbon film of the present disclosure is a carbon film made of a carbon nanotube assembly, wherein a pore distribution curve of the carbon film indicating the relationship between the pore size and the Log differential pore capacity obtained from an adsorption isotherm at 77 K of liquid nitrogen based on the Barrett-Joyner-Halenda method has a peak in which the Log differential pore capacity is maximized within a pore size range of 10 nm or more and 100 nm or less, and the value of the Log differential pore capacity at the peak is 1.2 cm.sup.3/g or more.

Disclosed here is a method of fabricating a covalently reinforced carbon nanotube (CNT) assembly. The method includes producing a CNT assembly by pulling entangled CNTs from a CNT array fabricated on a substrate, the CNT assembly including a plurality of CNTs that are aligned; and creating covalent bonding between the CNTs of the CNT assembly by applying a high energy ion irradiation to the CNT assembly.

Disclosed here is a method of fabricating a covalently reinforced carbon nanotube (CNT) assembly. The method includes producing a CNT assembly by pulling entangled CNTs from a CNT array fabricated on a substrate, the CNT assembly including a plurality of CNTs that are aligned; and creating covalent bonding between the CNTs of the CNT assembly by applying a high energy ion irradiation to the CNT assembly.

A carbon nanotube assembly satisfies at least one of the following conditions (1) to (3): (1) an FT-IR spectrum of a CNT dispersion obtained by dispersing the CNT assembly has a peak based on plasmon resonance of the CNTs in a wave number range of greater than 300 cm.sup.−1 and 2000 cm.sup.−1 or less; (2) the highest peak in a differential pore capacity distribution of the CNT assembly is located within a pore size range of more than 100 nm and less than 400 nm; and (3) a two-dimensional spatial frequency spectrum of an electronic micrographic image of the CNT assembly has at least one peak within a range of 1 μm.sup.−1 or more and 100 μm.sup.−1 or less.