CN101851383B - Conductive polymer composite material and preparation method thereof - Google Patents

Conductive polymer composite material and preparation method thereof Download PDF

Info

Publication number
CN101851383B
CN101851383B CN2010101960113A CN201010196011A CN101851383B CN 101851383 B CN101851383 B CN 101851383B CN 2010101960113 A CN2010101960113 A CN 2010101960113A CN 201010196011 A CN201010196011 A CN 201010196011A CN 101851383 B CN101851383 B CN 101851383B
Authority
CN
China
Prior art keywords
conductive
polymer composite
conductive filler
conductive polymer
filler material
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.)
Expired - Fee Related
Application number
CN2010101960113A
Other languages
Chinese (zh)
Other versions
CN101851383A (en
Inventor
黄凌峰
黄国清
陈海波
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.)
Shenzhen Ouxun Electronic Co ltd
Shenzhen Dongweifeng Electronic Technology Co ltd
Original Assignee
Shenzhen Ouxun Electronic Co ltd
Shenzhen Dongweifeng Electronic Technology 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 Shenzhen Ouxun Electronic Co ltd, Shenzhen Dongweifeng Electronic Technology Co ltd filed Critical Shenzhen Ouxun Electronic Co ltd
Priority to CN2010101960113A priority Critical patent/CN101851383B/en
Publication of CN101851383A publication Critical patent/CN101851383A/en
Application granted granted Critical
Publication of CN101851383B publication Critical patent/CN101851383B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Processes Of Treating Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention relates to a conductive polymer composite material and a preparation method thereof. The conductive polymer composite material comprises the following components in weight percentage: 80-95% of polyfluortetraethylene and 5-20% of conductive filler. The grain size of the polyfluortetraethylene as a raw material is 0.1-500 micrometers; and the conductive filler is one of conductive carbon black powder and graphite powder or the mixture thereof, wherein the grain size of the conductive carbon black powder is 10-200 nanometers, and the grain size of the graphite powder is 20-5000 nanometers. The preparation method comprises the following steps of: a. mixing and ball-milling conductive fillers and an alkaline aqueous solution; b. stirring and heating a polyfluortetraethylene emulsion; c. adding the aqueous solution of the conductive filler in the polyfluortetraethylene emulsion and then continuously stirring; and d. filtering the mixture of the polyfluortetraethylene and the conductive filler, pushing the settled and dried mixture into a thin long-strip shape, repeatedly and thermally rolling the mixture to form a strip-shaped belt, and then carrying out thermal treatment to obtain the conductive polymer composite material. The composite material has the characteristics of wide temperature range, easy adjustment of electric conductivity, stable mechanical property and the like.

Description

Conductive polymer composite and preparation method thereof
[technical field]
The present invention relates to polymer composite, particularly relate to a kind of conductive polymer composite and preparation method thereof with conducting function.
[background technology]
Plastics are known by people as a kind of insulating material.And, expanding himself performance in order to change the attribute of plastics, people expand to the electro-conductive material field with it, develop the novel material with conductivity.Conductive plastics is a kind of macromolecular material, is active research development field very in the world at present, and the pure laboratory study from the initial stage develops into the applied research stage, becomes electronic material of new generation.
Tetrafluoroethylene is a kind of widely used macromolecular material, and it has excellent chemical stability, erosion resistance, stopping property, high lubricated not viscosity, electrical insulating property and good anti-aging endurance, heatproof excellence.Though tetrafluoroethylene has the performance of above-mentioned excellence, it does not have conducting function, thereby its Application Areas still has certain limitation.
[summary of the invention]
The present invention is intended to make full use of the excellent properties of tetrafluoroethylene, and expands its Application Areas, and a kind of broad application temperature range is provided, and electric conductivity is easily adjusted, the conductive polymer composite that the mechanical property of materials is stable.
The present invention also aims to provide the preparation method of this conductive polymer composite.
For achieving the above object, the invention provides a kind of conductive polymer composite, its weight percent consists of:
Tetrafluoroethylene 80%~95%;
Conductive filler material 5%~20%.
The preferred weight percent of this conductive polymer composite consists of:
Tetrafluoroethylene 85%~90%;
Conductive filler material 10%~15%.
The particle diameter of tetrafluoroethylene raw material is 0.1~500 micron.
Conductive filler material is a kind of or its mixture in conductive carbon black powder, the Graphite Powder 99.
The particle diameter of conductive carbon black powder is 10~200 nanometers.
The particle diameter of Graphite Powder 99 is 20~5000 nanometers.
The invention provides the preparation method of this matrix material, this method comprises the steps:
A, be that 5~20% alkaline aqueous solution mixes mutually by 1: 5~10 weight ratio, with mixture ball milling 4~12 hours with conductive filler material and weight percent concentration;
B, take by weighing ptfe emulsion,, be heated 60~80 ℃ in the time of stirring ptfe emulsion electric mixer high-speed stirring in the ratio of conductive filler material and tetrafluoroethylene;
C, the aqueous solution of conductive filler material in the step (a) is joined in the ptfe emulsion in the stirring, continue again to stir 0.2~1 hour;
D, with the mixture filtration of tetrafluoroethylene in the step (c) with conductive filler material, after the temperature more than 100 ℃ sinks to the bottom oven dry, be forced into thin strip in the temperature more than 50 ℃, through forming the bar shaped ribbon after the hot roll extrusion repeatedly, through heat-treated more than 200 ℃, obtain conductive polymer composite again.
Described ptfe emulsion is the decentralized ptfe emulsion of mass percent concentration less than 50wt%, and its solvent is a water.
Contribution of the present invention is, it is with the composite functional material of tetrafluoroethylene exploitation becoming with conducting function, can not only give full play to the deep-etching of strong oxidizers such as the acid of tetrafluoroethylene self salt tolerant, nitric acid, chloroazotic acid, sulfuric acid, hydrofluoric acid and multiple organic solvent, and can greatly expand its Application Areas, tetrafluoroethylene conduction interchanger and pipeline with this matrix material production, improved the heat transfer coefficient of product, having solved in the pipe-line transportation material process friction and having produced an electrostatic difficult problem, and product can be between-190 ℃~250 ℃ steady operation.Matrix material broad application temperature range of the present invention, electric conductivity is easily adjusted, and the mechanical property of materials is stable, and the preparation method is simple, and is cheap, and process stabilizing is with short production cycle.
[embodiment]
The following example is to further explanation of the present invention and explanation, and the present invention is not constituted any limitation.
Powdered graphite 1kg and the median size that 2: 1 by weight percentage with median size was 250 nanometers is after the conductive carbon black 0.5kg of 100 nanometers mixes mutually, to form conductive filler material.This conductive filler material is joined in the NaOH aqueous solution that 10.5kg concentration is 8wt%, mixture ball milling in ball mill was mixed 6 hours.By conductive filler material and tetrafluoroethylene weight ratio is to measure the ptfe emulsion of respective volume at 1: 9, getting mass percent concentration is the ptfe emulsion 33.75kg of 40wt%, this emulsion is heated to 70 ℃, carry out violent mechanical stirring in the heat-processed, the stirring-head rotating speed is 750 rev/mins.Conductive filler material slurry behind the ball milling is joined in the ptfe emulsion that is stirring, continue to stir after 15 minutes, with the said mixture strainer filtering, after 120 ℃ temperature thorough drying, in the pushing machine, be forced into the bar of diameter 7mm, this bar is rolled into the bar shaped ribbon that thickness is 0.5mm through roller press, again through the thermal treatment of 220 ℃ of temperature, promptly obtain to have the matrix material of conducting function, after tested, its surface resistivity is 2.4S/cm.

Claims (2)

1. the preparation method of a conductive polymer composite, its feature is stored in, and it comprises the steps:
A, be that 5~20% alkaline aqueous solution mixes mutually by 1: 5~10 weight ratio, with mixture ball milling 4~12 hours with conductive filler material and weight percent concentration;
B, take by weighing ptfe emulsion,, be heated 60~80 ℃ in the time of stirring ptfe emulsion electric mixer high-speed stirring in the ratio of conductive filler material and tetrafluoroethylene;
C, the aqueous solution of conductive filler material in the step (a) is joined in the ptfe emulsion in the stirring, continue again to stir 0.2~1 hour;
D, with the mixture filtration of tetrafluoroethylene in the step (c) with conductive filler material, after the temperature more than 100 ℃ sinks to the bottom oven dry, be forced into thin strip in the temperature more than 50 ℃, through forming the bar shaped ribbon after the hot roll extrusion repeatedly, again through heat-treated more than 200 ℃, obtain conductive polymer composite, the weight percent of described conductive polymer composite consists of: tetrafluoroethylene 80%~95%, conductive filler material 5%~20%.
2. the preparation method of conductive polymer composite according to claim 1 is characterized in that described ptfe emulsion is the decentralized ptfe emulsion of mass percent concentration less than 50wt%, and its solvent is a water.
CN2010101960113A 2010-06-09 2010-06-09 Conductive polymer composite material and preparation method thereof Expired - Fee Related CN101851383B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010101960113A CN101851383B (en) 2010-06-09 2010-06-09 Conductive polymer composite material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010101960113A CN101851383B (en) 2010-06-09 2010-06-09 Conductive polymer composite material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN101851383A CN101851383A (en) 2010-10-06
CN101851383B true CN101851383B (en) 2011-11-30

Family

ID=42803074

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010101960113A Expired - Fee Related CN101851383B (en) 2010-06-09 2010-06-09 Conductive polymer composite material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN101851383B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102604281A (en) * 2012-02-14 2012-07-25 南昌航空大学 Preparation method of crosslinking-free polymer-based high-temperature PTC (positive temperature coefficient) material
EP2871697A4 (en) * 2012-07-06 2016-05-11 Daikin Ind Ltd Sheet, electrode and fuel cell
CN105504612A (en) * 2016-02-01 2016-04-20 天津市天塑科技集团有限公司 Preparation method of anti-static polytetrafluoroethylene thin film
CN109401148A (en) * 2018-11-12 2019-03-01 佛山市纳博工业设备有限公司 A kind of resin conductive ring of high-pressure electrostatic spray gun and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101481483A (en) * 2009-02-12 2009-07-15 广州市东泓橡塑制品有限公司 Antistatic teflon film and preparation thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101481483A (en) * 2009-02-12 2009-07-15 广州市东泓橡塑制品有限公司 Antistatic teflon film and preparation thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
张永强等."石墨对聚四氟乙烯(PTFE)抗静电性能的影响".《热加工工艺技术与材料研究》.2009,(第11期),71-73.
张永强等."石墨对聚四氟乙烯(PTFE)抗静电性能的影响".《热加工工艺技术与材料研究》.2009,(第11期),71-73. *

Also Published As

Publication number Publication date
CN101851383A (en) 2010-10-06

Similar Documents

Publication Publication Date Title
Yao et al. BaTiO3-carbon nanotube/polyvinylidene fluoride three-phase composites with high dielectric constant and low dielectric loss
CN101798462B (en) Graphene/conductive polymer composite film and preparation method thereof
CN101851383B (en) Conductive polymer composite material and preparation method thereof
US10435571B2 (en) Method for preparing carbon nanotube, and dispersion composition of carbon nanotube
CN103253740B (en) Preparation method of three-dimensional hierarchical graphene/porous carbon composite capacitive type desalination electrode
CN103937234A (en) Thermal conductive plastic applying modified carbon material, and preparation method thereof
CN104650581A (en) Preparation method of graphene/polyamide dielectric composite material
CN104530614A (en) Porous polyvinylidene fluoride-carbon nanotube composite material and preparation method thereof
Wang et al. Nanostructured Mn–Cu binary oxides for supercapacitor
Zhu et al. Optimizing the thermoelectric properties of PEDOT: PSS films by combining organic co-solvents with inorganic base
Dhibar et al. Copper chloride‐doped polyaniline/multiwalled carbon nanotubes nanocomposites: Superior electrode material for supercapacitor applications
Niu et al. Facile preparation of flexible all organic PEDOT: PSS/methyl cellulose thermoelectric composite film by a screen printing process
CN103450463A (en) Preparation method of poly(3,4-ethylenedioxythiophene)/reduced graphene oxide/Co3O4 (PEDOT-RGO-Co3O4) nano wave-absorbing material
Zhu et al. Green DES mixture as a surface treatment recipe for improving the thermoelectric properties of PEDOT: PSS films
CN106783199B (en) A kind of infiltration has high temperature pyrolysis product of hollow carbon sphere of melamine and preparation method thereof
Wang et al. One-step interfacial synthesis and thermoelectric properties of Ag/Cu-poly (3, 4-ethylenedioxythiophene) nanostructured composites
CN103467986A (en) Nano titanium carbide/polyimide composite material modified by small organic molecules
CN105575674B (en) Graphene/absorbent charcoal composite material and preparation method, ultracapacitor
CN110482540B (en) Preparation method of graphene oxide powder with good dispersibility
CN102504450B (en) High-dielectric-constant polymer-potassium salt composite film material and preparation method thereof
CN107364890B (en) Liquid phase stripping method of two-dimensional molybdenum disulfide nano material, molybdenum disulfide dispersing method and application
CN101168596A (en) High yield method for synthesizing nano polyaniline
Khutia et al. Study of electrical relaxation mechanism of TiO2 doped Bi-polymer systems
CN103013004A (en) Carbon/silicon core-shell structure-polymer high-dielectric composite material
Cao et al. MWCNTs/SiO2 composite system: carrier transmission, twin-percolation and dielectric properties

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20111130

Termination date: 20160609