US20060006367A1 - Carbon nanotube suspension - Google Patents

Carbon nanotube suspension Download PDF

Info

Publication number
US20060006367A1
US20060006367A1 US10/883,722 US88372204A US2006006367A1 US 20060006367 A1 US20060006367 A1 US 20060006367A1 US 88372204 A US88372204 A US 88372204A US 2006006367 A1 US2006006367 A1 US 2006006367A1
Authority
US
United States
Prior art keywords
carbon nanotube
suspension
mixture
dispersant
antifoam
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/883,722
Inventor
Chun-Yen Hsiao
Yu-An Li
Jin-Lung Tsai
Kuei-Wen Cheng
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TECO NANCOTECH Co Ltd
Original Assignee
TECO NANCOTECH Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by TECO NANCOTECH Co Ltd filed Critical TECO NANCOTECH Co Ltd
Priority to US10/883,722 priority Critical patent/US20060006367A1/en
Assigned to TECO NANCOTECH CO., LTD. reassignment TECO NANCOTECH CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHENG, KUEI-WEN, HSIAO, CHUN-YEN, LI, YU-AN, TSAI, JIN-LUNG
Publication of US20060006367A1 publication Critical patent/US20060006367A1/en
Priority to US11/669,300 priority patent/US7378074B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/24Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y10/00Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J31/00Cathode ray tubes; Electron beam tubes
    • H01J31/08Cathode ray tubes; Electron beam tubes having a screen on or from which an image or pattern is formed, picked up, converted, or stored
    • H01J31/10Image or pattern display tubes, i.e. having electrical input and optical output; Flying-spot tubes for scanning purposes
    • H01J31/12Image or pattern display tubes, i.e. having electrical input and optical output; Flying-spot tubes for scanning purposes with luminescent screen
    • H01J31/123Flat display tubes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J9/00Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
    • H01J9/02Manufacture of electrodes or electrode systems
    • H01J9/022Manufacture of electrodes or electrode systems of cold cathodes
    • H01J9/025Manufacture of electrodes or electrode systems of cold cathodes of field emission cathodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J2201/00Electrodes common to discharge tubes
    • H01J2201/30Cold cathodes
    • H01J2201/304Field emission cathodes
    • H01J2201/30446Field emission cathodes characterised by the emitter material
    • H01J2201/30453Carbon types
    • H01J2201/30469Carbon nanotubes (CNTs)
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S977/00Nanotechnology
    • Y10S977/70Nanostructure
    • Y10S977/734Fullerenes, i.e. graphene-based structures, such as nanohorns, nanococoons, nanoscrolls or fullerene-like structures, e.g. WS2 or MoS2 chalcogenide nanotubes, planar C3N4, etc.
    • Y10S977/742Carbon nanotubes, CNTs
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S977/00Nanotechnology
    • Y10S977/70Nanostructure
    • Y10S977/832Nanostructure having specified property, e.g. lattice-constant, thermal expansion coefficient
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S977/00Nanotechnology
    • Y10S977/70Nanostructure
    • Y10S977/832Nanostructure having specified property, e.g. lattice-constant, thermal expansion coefficient
    • Y10S977/835Chemical or nuclear reactivity/stability of composition or compound forming nanomaterial

Definitions

  • the present invention relates in general to a carbon nanotube suspension, and more particularly, to a solvent containing carbon nanotube suspending therein.
  • the carbon nanotube suspension can be used for forming an electron-emission source of a field-emission display.
  • the field-emission display is a very newly developed technology. Being self-illuminant, such type of display does not require a back light source like the liquid crystal display (LCD). In addition to the better brightness, the viewing angle is broader, power consumption is lower, response speed is faster (no residual image), and the operation temperature range is larger.
  • the image quality of the field-emission display is similar to that of the conventional cathode ray tube (CRT) display, while the dimension of the field-emission display is much thinner and lighter compared to the cathode ray tube display. Therefore, it is foreseeable that the field-emission display may replace the liquid crystal display in the market. Further, the fast growing nanotechnology enables nano-material to be applied in the field-emission display, such that the technology of field-emission display will be commercially available.
  • FIG. 1 shows a conventional triode field-emission display, which includes an anode plate 10 and a cathode plate 20 .
  • a spacer 14 is placed in the vacuum region between the anode plate 10 and the cathode plate 20 to provide isolation and support thereof.
  • the anode plate 10 includes an anode substrate 11 , an anode conductive layer 12 and a phosphor layer 13 .
  • the cathode plate 20 includes a cathode substrate 21 , a cathode conductive layer 22 , an electron emission layer 23 , a dielectric layer 24 and a gate layer 25 .
  • a potential difference is provided to the gate layer 25 to induce electron beam emission from the electron emission layer 23 .
  • the high voltage provided by the anode conductive layer 12 accelerates the electron beam with sufficient momentum to impinge the phosphors layer 13 of the anode plate 10 , which is then excited to emit a light.
  • the lately developed carbon nanotube has been applied to form the electron-emission source of a field-emission display due to its specific characteristics.
  • the carbon nanotube is typically formed on a cathode plate for generating electron beams.
  • the carbon-nanotube electron-emission source is formed by screen printing and has viscosity as high as 100,000 cps. With such high viscosity, it is very difficult to obtain an even surface.
  • the distance between the electron-emission layer and the gate layer of the same cathode unit is non-uniform, such that the electric field cannot be uniform to generate uniform electron beams in each position. That is, when the gap between the electron-emission layer and the gate layer is shorter, the electric field is larger, and more electrons are emitted.
  • the very high viscosity of the carbon nanotube mixture is very difficult to distribute. Therefore, dispersing technique based on its mechanism and physical property has is required. Even when the carbon nanotube mixture is distributed by mechanical and physical property, an even thickness is still difficult to obtain. Therefore, non-uniform electron beams are emitted. As a result, uneven brightness in a single luminescent unit occurs, such that the image quality is degraded.
  • adhesion additive such as glass powder is often required to further complicate the process.
  • a carbon nanotube suspension is provide to serve as the source material for the electron emission source of a field-emission display.
  • the electron-emission source can be easily formed by a coating process.
  • a carbon nanotube suspension is provided with a reduced viscosity such that it is more easily and evenly distributed on a surface.
  • a carbon nanotube suspension is provided with a viscosity sufficiently low that it can be coated with an even thickness.
  • the carbon nanotube suspension as discussed above uses water as the solvent, and dispersant, stabilizer, coalescing aid, adhesion promoter and carbon nanotube as the solutes to form a low-viscosity solution with carbon nanotube suspending therein.
  • FIG. 1 shows a cross sectional view of a conventional triode field-emission display
  • FIG. 2 shows the process of forming the carbon nanotube suspension
  • FIGS. 3 a through 3 d show the fabrication process of the electron emission source using the carbon nanotube suspension.
  • a carbon nanotube suspension is provided using water as the solvent, which is added with dispersant, stabilizer, coalescing aid, adhesion promoter and antifoam to form a low-viscosity solution.
  • a carbon nanotube no longer than 1 micron is then immersed in the low-viscosity solution to form the carbon nanotube suspension.
  • the proportion of the solutes and the nanotube is as follows:
  • step 50 water is used as the solvent.
  • the total mass of the solvent is used as a reference for calculating the weight percentage of each solute.
  • step 51 5% of organic methyl alkyl eikonogen (dispersant) and 5% of antifoam are added in the solvent.
  • step 52 10% of carbon nanotube is added in the mixture of water, dispersant and antifoam.
  • step 53 the mixture obtained in step 52 is vibrated and stirred using ultrasonic vibration technique. The vibration and stir are performed for about 3 hours.
  • step 54 1% of ammonia (stabilizer) is added in the vibrated mixture, and the mixture added with ammonia is further stirred.
  • step 55 5% of aluminum sodium sulfate (coalescing aid), 10% of silane coupling agent (coalescing aid), 2.8% of PVA (adhesion promoter) and 2% of ethyl hydroxide (dispersant) are added in the mixture.
  • step 56 the mixture obtained from step 55 is sieved by a 500 mesh to form a low-viscosity carbon nanotube suspension.
  • the above composition provides a carbon nanotube suspension with viscosity as low as 24 pcs, while the proportion of solid component is about 14%.
  • Such carbon nanotube suspension has much lower viscosity compared to currently available carbon nanotube suspension. It can be easily coated into a uniform form.
  • the dispersant performs chemical dispersion such that the carbon nanotube in the suspension will not agglomerate. Therefore, the carbon nanotube suspension can be used for forming uniform electron-emission layer in a field-emission display.
  • the carbon nanotube suspension can be used for forming the electron-emission source on a cathode substrate by vacuum sintering process, in which the carbon nanotube of the suspension is directly attached to the cathode substrate to form the electron emission layer. Therefore, no adhesive additive such as glass powder is required. As a result, the deposit density of the carbon nanotube in the suspension will not be diluted by addition of the adhesive additive.
  • FIGS. 2 shows the method for fabricating the electron-emission layer on a cathode substrate using the carbon nanotube suspension.
  • a negative photoresist is used, and photolithography and etching process is performed for forming and patterning the electron-emission layer.
  • the carbon nanotube electron-emission layer is formed by vacuum sintering process.
  • a cathode substrate 1 is provided.
  • a photoresist layer 2 is formed on the cathode substrate 1 by photolithography and etching process. By such patterning technique, a plurality of discrete electron emission regions 3 is formed.
  • the carbon nanotube suspension is directly coated in the electron-emission regions 3 .
  • etching and development process is performed to remove the photoresist layer.
  • Vacuum sintering is performed to attach the electron-emission layer on the cathode substrate 1 as shown.
  • the electron-emission layer fabricated from the carbon nanotube suspension by the above method has a very uniform thickness. Therefore, the image quality of the field-emission display is greatly enhanced.

Abstract

A carbon nanotube suspension uses water as the basic solvent added with dispersant, stabilizer, coalescing aid, adhesion promoter, and a carbon nanotube. The basic solvent and the above solutes form a low viscosity solvent with carbon nanotube suspending therein. Therefore, the carbon nanotube suspension is formed to serve as a source material of the electron emission source of a field-emission display. That is, the carbon nanotube can be coated on a surface for forming the carbon nanotube electron-emission layer.

Description

    BACKGROUND OF THE INVENTION
  • The present invention relates in general to a carbon nanotube suspension, and more particularly, to a solvent containing carbon nanotube suspending therein. The carbon nanotube suspension can be used for forming an electron-emission source of a field-emission display.
  • The field-emission display is a very newly developed technology. Being self-illuminant, such type of display does not require a back light source like the liquid crystal display (LCD). In addition to the better brightness, the viewing angle is broader, power consumption is lower, response speed is faster (no residual image), and the operation temperature range is larger. The image quality of the field-emission display is similar to that of the conventional cathode ray tube (CRT) display, while the dimension of the field-emission display is much thinner and lighter compared to the cathode ray tube display. Therefore, it is foreseeable that the field-emission display may replace the liquid crystal display in the market. Further, the fast growing nanotechnology enables nano-material to be applied in the field-emission display, such that the technology of field-emission display will be commercially available.
  • FIG. 1 shows a conventional triode field-emission display, which includes an anode plate 10 and a cathode plate 20. A spacer 14 is placed in the vacuum region between the anode plate 10 and the cathode plate 20 to provide isolation and support thereof. The anode plate 10 includes an anode substrate 11, an anode conductive layer 12 and a phosphor layer 13. The cathode plate 20 includes a cathode substrate 21, a cathode conductive layer 22, an electron emission layer 23, a dielectric layer 24 and a gate layer 25. A potential difference is provided to the gate layer 25 to induce electron beam emission from the electron emission layer 23. The high voltage provided by the anode conductive layer 12 accelerates the electron beam with sufficient momentum to impinge the phosphors layer 13 of the anode plate 10, which is then excited to emit a light.
  • The lately developed carbon nanotube has been applied to form the electron-emission source of a field-emission display due to its specific characteristics. The carbon nanotube is typically formed on a cathode plate for generating electron beams. Currently, the carbon-nanotube electron-emission source is formed by screen printing and has viscosity as high as 100,000 cps. With such high viscosity, it is very difficult to obtain an even surface. As a result, the distance between the electron-emission layer and the gate layer of the same cathode unit is non-uniform, such that the electric field cannot be uniform to generate uniform electron beams in each position. That is, when the gap between the electron-emission layer and the gate layer is shorter, the electric field is larger, and more electrons are emitted. The very high viscosity of the carbon nanotube mixture is very difficult to distribute. Therefore, dispersing technique based on its mechanism and physical property has is required. Even when the carbon nanotube mixture is distributed by mechanical and physical property, an even thickness is still difficult to obtain. Therefore, non-uniform electron beams are emitted. As a result, uneven brightness in a single luminescent unit occurs, such that the image quality is degraded. In addition, although the carbon nanotube mixture has very high viscosity, the adhesion is insufficient. Therefore, adhesion additive such as glass powder is often required to further complicate the process.
  • BRIEF SUMMARY OF THE INVENTION
  • A carbon nanotube suspension is provide to serve as the source material for the electron emission source of a field-emission display. The electron-emission source can be easily formed by a coating process.
  • A carbon nanotube suspension is provided with a reduced viscosity such that it is more easily and evenly distributed on a surface.
  • A carbon nanotube suspension is provided with a viscosity sufficiently low that it can be coated with an even thickness.
  • The carbon nanotube suspension as discussed above uses water as the solvent, and dispersant, stabilizer, coalescing aid, adhesion promoter and carbon nanotube as the solutes to form a low-viscosity solution with carbon nanotube suspending therein.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The above objects and advantages of the present invention will be become more apparent by describing in detail exemplary embodiments thereof with reference to the attached drawings in which:
  • FIG. 1 shows a cross sectional view of a conventional triode field-emission display;
  • FIG. 2 shows the process of forming the carbon nanotube suspension; and
  • FIGS. 3 a through 3 d show the fabrication process of the electron emission source using the carbon nanotube suspension.
  • DETAILED DESCRIPTION OF THE INVENTION
  • A carbon nanotube suspension is provided using water as the solvent, which is added with dispersant, stabilizer, coalescing aid, adhesion promoter and antifoam to form a low-viscosity solution. A carbon nanotube no longer than 1 micron is then immersed in the low-viscosity solution to form the carbon nanotube suspension. The proportion of the solutes and the nanotube is as follows:
    • 1. carbon nanotube: 5% to 20%;
    • 2. coalescing aid: 5% to 20%, including aluminum sodium sulfate, silane coupling agent, alkyd resin or tetra-ethyl-ortho-silicate (TEOS), or the combination of any of these components, such that the suspension can be easily attached to the glass substrate of the field-emission display;
    • 3. adhesion promoter: 1% to 5%, including PVA, PVP, methyl cellulose, ethyl cellulose, sodium polyacrylate, or ammonium polyacrylate for increasing adhesion of the suspension, so as to control the film thickness.
    • 4. stablizer: 0.5% to 5%, including one of ammonia, potassium hydroxide, and sodium hydroxide, such that storage life is longer, and the carbon nanotub has sufficient time to disperse;
    • 5. dispersant: 1% to 10%, including ethyl hydroxide and organic alkyl eikonogen for motivating the nanotube dispersing in the suspension; and
    • 6. antifoam: 1% to 10%, including polypropylene glycol (PPG) to eliminate foams or bubbles caused by stir.
  • The composition and fabrication method are illustrated in FIG. 2. In step 50, water is used as the solvent. In the mixing process, the total mass of the solvent is used as a reference for calculating the weight percentage of each solute.
  • In step 51, 5% of organic methyl alkyl eikonogen (dispersant) and 5% of antifoam are added in the solvent.
  • In step 52, 10% of carbon nanotube is added in the mixture of water, dispersant and antifoam.
  • In step 53, the mixture obtained in step 52 is vibrated and stirred using ultrasonic vibration technique. The vibration and stir are performed for about 3 hours.
  • In step 54, 1% of ammonia (stabilizer) is added in the vibrated mixture, and the mixture added with ammonia is further stirred.
  • In step 55, 5% of aluminum sodium sulfate (coalescing aid), 10% of silane coupling agent (coalescing aid), 2.8% of PVA (adhesion promoter) and 2% of ethyl hydroxide (dispersant) are added in the mixture.
  • In step 56, the mixture obtained from step 55 is sieved by a 500 mesh to form a low-viscosity carbon nanotube suspension.
  • The above composition provides a carbon nanotube suspension with viscosity as low as 24 pcs, while the proportion of solid component is about 14%. Such carbon nanotube suspension has much lower viscosity compared to currently available carbon nanotube suspension. It can be easily coated into a uniform form. The dispersant performs chemical dispersion such that the carbon nanotube in the suspension will not agglomerate. Therefore, the carbon nanotube suspension can be used for forming uniform electron-emission layer in a field-emission display.
  • Preferably, the carbon nanotube suspension can be used for forming the electron-emission source on a cathode substrate by vacuum sintering process, in which the carbon nanotube of the suspension is directly attached to the cathode substrate to form the electron emission layer. Therefore, no adhesive additive such as glass powder is required. As a result, the deposit density of the carbon nanotube in the suspension will not be diluted by addition of the adhesive additive.
  • FIGS. 2 shows the method for fabricating the electron-emission layer on a cathode substrate using the carbon nanotube suspension. In FIG. 3, a negative photoresist is used, and photolithography and etching process is performed for forming and patterning the electron-emission layer. The carbon nanotube electron-emission layer is formed by vacuum sintering process.
  • As shown in FIG. 3 a, a cathode substrate 1 is provided.
  • In FIG. 3 b, a photoresist layer 2 is formed on the cathode substrate 1 by photolithography and etching process. By such patterning technique, a plurality of discrete electron emission regions 3 is formed.
  • As shown in FIG. 3 c, the carbon nanotube suspension is directly coated in the electron-emission regions 3.
  • In FIG. 3 d, etching and development process is performed to remove the photoresist layer. Vacuum sintering is performed to attach the electron-emission layer on the cathode substrate 1 as shown.
  • The electron-emission layer fabricated from the carbon nanotube suspension by the above method has a very uniform thickness. Therefore, the image quality of the field-emission display is greatly enhanced.
  • While the present invention has been particularly shown and described with reference to preferred embodiments thereof, it will be understood by those of ordinary skill in the art the various changes in form and details may be made therein without departing from the spirit and scope of the present invention as defined by the appended claims.

Claims (16)

1. A carbon nanotube suspension, comprising:
water;
5% to 20% of carbon nanotube;
5% to 20% of coalescing aid;
1% to 5% of adhesion promoter;
0.5% to 5% of stablizer;
1% to 10% of dispersant; and
1% to 10% of antifoam.
2. The suspension of claim 1, wherein the carbon nanotube is no longer than 1 micron.
3. The suspension of claim 1, wherein the dispersant includes ethyl hydroxide or organic methyl eikonogen.
4. The suspension of claim 1, wherein the antifoam includes polypropylene glycol (PPG).
5. The suspension of claim 1, wherein the coalescing aid includes one or a combination of aluminum sodium sulfate, silane coupling agent, alkyd resin or tetra-ethyl-ortho-silicate (TEOS).
6. The suspension of claim 1, wherein the adhesion promoter includes one of PVA, PVP, methyl cellulose, ethyl cellulose, sodium polyacrylate and ammonium polyacrylate.
7. The suspension of claim 1, wherein the stablizer includes one of sodium hydroxide, potassium hydroxide and ammonia.
8. A method of forming carbon nanotube suspension, comprising:
providing water as a solvent, uniformly adding 1% to 10% of dispersant and 1% to 10% antifoam in the solvent;
adding 5% to 20% of carbon nanotube;
vibrating and stirring the mixture of water, dispersant, antifoam and carbon nanotube for a predetermined period of time;
adding stablizer in the mixture and stirring the mixture;
adding 5% to 20% of coalescing aid, 1% to 5% of adhesion promoter and stirring the mixture; and
sieving the mixture by a mesh.
9. The method of claim 8, wherein the carbon nanotube is shorter than 1 micron.
10. The method of claim 8, wherein the dispersant includes ethyl hydroxide or organic methyl eikonogen.
11. The method of claim 8, wherein the antifoam includes polypropylene glycol (PPG).
12. The method of claim 8, wherein the coalescing aid includes one or more than one of aluminum sodium sulfate, silane coupling agent, alkyd resin and tetra-ethyl-ortho-silicate (TEOS).
13. The method of claim 8, wherein the adhesion promoter includes PVA, PVP, methyl cellulose, ethyl cellulose, sodium polyacrylate or ammonium polyacrylate.
14. The method of claim 8, wherein the stablizer includes sodium hydroxide, potassium hydroxide or ammonia.
15. The method of claim 8, wherein the vibration and stirring process includes an ultrasonic vibration and stirring process.
16. The method of claim 8, wherein a 500 mesh is used for sieving the mixture.
US10/883,722 2004-07-06 2004-07-06 Carbon nanotube suspension Abandoned US20060006367A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US10/883,722 US20060006367A1 (en) 2004-07-06 2004-07-06 Carbon nanotube suspension
US11/669,300 US7378074B2 (en) 2004-07-06 2007-01-31 Method of forming a uniform carbon nanotube electron-emission layer in a field emission display

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10/883,722 US20060006367A1 (en) 2004-07-06 2004-07-06 Carbon nanotube suspension

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/669,300 Division US7378074B2 (en) 2004-07-06 2007-01-31 Method of forming a uniform carbon nanotube electron-emission layer in a field emission display

Publications (1)

Publication Number Publication Date
US20060006367A1 true US20060006367A1 (en) 2006-01-12

Family

ID=35540352

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/883,722 Abandoned US20060006367A1 (en) 2004-07-06 2004-07-06 Carbon nanotube suspension
US11/669,300 Expired - Fee Related US7378074B2 (en) 2004-07-06 2007-01-31 Method of forming a uniform carbon nanotube electron-emission layer in a field emission display

Family Applications After (1)

Application Number Title Priority Date Filing Date
US11/669,300 Expired - Fee Related US7378074B2 (en) 2004-07-06 2007-01-31 Method of forming a uniform carbon nanotube electron-emission layer in a field emission display

Country Status (1)

Country Link
US (2) US20060006367A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070267602A1 (en) * 2006-05-19 2007-11-22 Shie-Heng Lee Method of Manufacturing Carbon Nanotubes Paste
CN100455509C (en) * 2007-03-29 2009-01-28 浙江大学 Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid
WO2009029182A2 (en) * 2007-08-21 2009-03-05 Oceanit Laboratories, Nic. Carbon nanomaterials dispersion and stabilization
US20090142576A1 (en) * 2007-11-30 2009-06-04 Tsinghua University Filter and method for making the same
TWI419835B (en) * 2007-12-14 2013-12-21 Hon Hai Prec Ind Co Ltd Filtering film and method of making the same
US20160002418A1 (en) * 2013-02-05 2016-01-07 3M Innovative Properties Company Graphic article
CN106276850A (en) * 2016-08-09 2017-01-04 武汉工程大学 High concentration, finely dispersed carbon nano tube suspension preparation method

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101389411B (en) * 2006-02-27 2010-12-01 东丽株式会社 Composition and preparation mehod of display device using the composition
US8273230B2 (en) * 2008-02-15 2012-09-25 Atomic Energy Council—Institute of Nuclear Research Method for making membrane fuel cell electrodes by low-voltage electrophoretic deposition of carbon nanomaterial-supported catalysts
CN101485962B (en) * 2008-11-06 2011-05-04 青岛大学 Simple method for dispersing carbon nano-tube

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6331262B1 (en) * 1998-10-02 2001-12-18 University Of Kentucky Research Foundation Method of solubilizing shortened single-walled carbon nanotubes in organic solutions
US6783746B1 (en) * 2000-12-12 2004-08-31 Ashland, Inc. Preparation of stable nanotube dispersions in liquids
US20060052509A1 (en) * 2002-11-01 2006-03-09 Mitsubishi Rayon Co., Ltd. Composition containing carbon nanotubes having coating thereof and process for producing them

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3607782B2 (en) * 1996-10-17 2005-01-05 東洋炭素株式会社 Single-wall nanotube separation / purification method and metal-encapsulated nanocapsule separation / purification method
CA2489423A1 (en) * 2002-06-14 2003-12-24 Hyperion Catalysis International, Inc. Electroconductive carbon fibril-based inks and coatings

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6331262B1 (en) * 1998-10-02 2001-12-18 University Of Kentucky Research Foundation Method of solubilizing shortened single-walled carbon nanotubes in organic solutions
US6783746B1 (en) * 2000-12-12 2004-08-31 Ashland, Inc. Preparation of stable nanotube dispersions in liquids
US20060052509A1 (en) * 2002-11-01 2006-03-09 Mitsubishi Rayon Co., Ltd. Composition containing carbon nanotubes having coating thereof and process for producing them

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070267602A1 (en) * 2006-05-19 2007-11-22 Shie-Heng Lee Method of Manufacturing Carbon Nanotubes Paste
CN100455509C (en) * 2007-03-29 2009-01-28 浙江大学 Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid
WO2009029182A2 (en) * 2007-08-21 2009-03-05 Oceanit Laboratories, Nic. Carbon nanomaterials dispersion and stabilization
WO2009029182A3 (en) * 2007-08-21 2009-07-09 Oceanit Lab Nic Carbon nanomaterials dispersion and stabilization
US20090142576A1 (en) * 2007-11-30 2009-06-04 Tsinghua University Filter and method for making the same
TWI419835B (en) * 2007-12-14 2013-12-21 Hon Hai Prec Ind Co Ltd Filtering film and method of making the same
US20160002418A1 (en) * 2013-02-05 2016-01-07 3M Innovative Properties Company Graphic article
CN106276850A (en) * 2016-08-09 2017-01-04 武汉工程大学 High concentration, finely dispersed carbon nano tube suspension preparation method

Also Published As

Publication number Publication date
US20070295940A1 (en) 2007-12-27
US7378074B2 (en) 2008-05-27

Similar Documents

Publication Publication Date Title
US7378074B2 (en) Method of forming a uniform carbon nanotube electron-emission layer in a field emission display
US6858981B2 (en) Electron emission source composition for field emission display device and field emission display device fabricated using same
US6146230A (en) Composition for electron emitter of field emission display and method for producing electron emitter using the same
US20060043872A1 (en) Electron emission device and fabricating method thereof
WO2002074879A1 (en) Fluorescent powder, process for producing the same, display panel, and flat display
US7999453B2 (en) Electron emitter and a display apparatus utilizing the same
JPWO2008111350A1 (en) Phosphor surface treatment method and flat panel display manufacturing method
US7247980B2 (en) Emitter composition using diamond, method of manufacturing the same and field emission cell using the same
JP2010198890A (en) Fluorescent material substrate and image display device, and methods for manufacture thereof
JP2005251748A (en) Manufacturing method of cathode substrate and flat panel display device including cathode substrate manufactured by method
EP1505621A1 (en) Emitter composition using diamond method of manufacturing the same and field emission cell using the same
CN105448620A (en) Field emission cathode and field emission device
US20060103287A1 (en) Carbon-nanotube cold cathode and method for fabricating the same
KR20030092730A (en) Flat panel display
JP2002509340A (en) Ion bombarded graphite electron emitter
US7541390B2 (en) Composition for preparing electron emitter, electron emitter produced by using the composition, and electron emission device comprising the electron emitter
US9552953B2 (en) Field emission cathode and field emission device
CN1313364C (en) Nano carbon tube suspensoid and its manufacturing method
US6204600B1 (en) Field emission device having floating electrode and conductive particle layer
KR100291786B1 (en) Manufacturing method of field emission display
TWI258789B (en) Carbon nanotube suspension
KR100447132B1 (en) Field emission display with spacer and method of adhesion the same
JP2005310647A (en) Field emission type display and its manufacturing method
CN105448624A (en) Field emission cathode preparation method
KR101151600B1 (en) Field emission device(fed) including carbon nanotube field emitter having a high electron emission

Legal Events

Date Code Title Description
AS Assignment

Owner name: TECO NANCOTECH CO., LTD., TAIWAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HSIAO, CHUN-YEN;LI, YU-AN;TSAI, JIN-LUNG;AND OTHERS;REEL/FRAME:015549/0583

Effective date: 20040706

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION