CN101525468B - Preparation method of low-resistance conductive plastic - Google Patents

Preparation method of low-resistance conductive plastic Download PDF

Info

Publication number
CN101525468B
CN101525468B CN200910058605.5A CN200910058605A CN101525468B CN 101525468 B CN101525468 B CN 101525468B CN 200910058605 A CN200910058605 A CN 200910058605A CN 101525468 B CN101525468 B CN 101525468B
Authority
CN
China
Prior art keywords
low
conductive plastic
resistance conductive
composition board
carbon felt
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.)
Active
Application number
CN200910058605.5A
Other languages
Chinese (zh)
Other versions
CN101525468A (en
Inventor
刘联
刘效疆
陈茂斌
冯秀丽
李晓兵
宋学兵
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.)
Sichuan Huantong Electronics Co.,Ltd.
Original Assignee
Institute of Electronic Engineering of CAEP
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 Institute of Electronic Engineering of CAEP filed Critical Institute of Electronic Engineering of CAEP
Priority to CN200910058605.5A priority Critical patent/CN101525468B/en
Publication of CN101525468A publication Critical patent/CN101525468A/en
Application granted granted Critical
Publication of CN101525468B publication Critical patent/CN101525468B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention relates to a low-resistance conductive plastic and a preparation method thereof. The low-resistance conductive plastic comprises the raw materials with the mass percentage: 30-85% of epoxide resin, 10-60% of curing agent, 0-3% of accelerant and 10-55% of carbon fiber felt. The preparation method of the low-resistance conductive plastic comprises the steps: the epoxide resin, the curing agent and the accelerant are put into a baking oven to be baked to be 30-150 DEG C, so that mixture A is obtained; the carbon fiber felt is dipped into the mixture A, and the mixed solution is put into a mould to be cured to obtain a clad plate; the clad plate is placed into concentrated sulfuric acid with the temperature of 20-150 DEG C to be stirred and processed by ultrasonic oscillation; then, the clad plate is taken out and put into hot water with the temperature of 50-90 DEG C; finally, the low-resistance conductive plastic is obtained after being washed by ultrasonic wave for a plurality of times and dried. The low-resistance conductive plastic has good electric conduction performance, can not be etched by vanadium electrolyte, resists electric pile overcharge, and is high in mechanical strength and low in cost.

Description

A kind of preparation method of low-resistance conductive plastic
Technical field
The invention belongs to the conductive plastic material field, be specifically related to a kind of preparation method of low-resistance conductive plastic.
Background technology
At present, use graphite cake in the vanadium cell usually, the thermoplastic conductive of use plastics are also arranged as pole plate as pole plate.The advantage of graphite cake is that resistance is little, and shortcoming is to be etched easily and poor toughness.Though the thermoplastic conductive plastics are not by anodal liquid etching, and good toughness, its resistance is bigger, the heavy-current discharge performance of restriction vanadium cell.Therefore, seek the important topic that another anti-etching, good toughness and the good conducting plates of conductivity become vanadium cell research.
(number of patent application is CN200510086201.9) discloses a kind of conductive plastics and working method thereof, processing unit (plant) in the Chinese patent literature, described conductive plastics comprises: the electro-conductive fiber of 0.1~45v%, the thermoplastics of 55~99v% and the processing aid of 0~3v%; This invents described conductive plastics by short carbon fiber overlap joint conduction, its electroconductibility is better than only adding the conductive plastics that Graphite Powder 99 is made conductive agent, weak point is that the carbon fiber of overlap joint has skim Resins, epoxy to intercept mutually, and resistivity is still bigger, and conductivity can not satisfy the needs of vanadium cell.
Summary of the invention
The technical problem to be solved in the present invention provides a kind of preparation method of low-resistance conductive plastic.
The preparation method of low-resistance conductive plastic of the present invention comprises the steps: successively
A) the raw materials quality per-cent prescription according to low-resistance conductive plastic quantitatively takes by weighing Resins, epoxy 30%~85%, solidifying agent 10%~60%, and promotor 0~3%, carbon felt 1%~55% is standby;
B) Resins, epoxy, solidifying agent and promotor are put into baking oven baking to 30 ℃~150 ℃, mix, stir evenly mixture A;
C) the carbon felt is immersed among the mixture A, makes and wherein do not stay bubble, take out and to put into mould, flatten, solidify composition board;
D) composition board after the above-mentioned curing is put into 20 ℃~150 ℃ the vitriol oil, stirred, adopt ultra-sonic oscillation to handle simultaneously 2 minutes to two hours;
E) take out composition board, put it in 50 ℃~90 ℃ the hot water, ultrasonic cleaning 3 times each 6 minutes, is dried moisture then;
Repeating step d) and step e) f), the composition board of oven dry moisture being dropped in the vitriol oil again, is 1 millimeter up to the surface corrosion degree of depth, cleans then and dries, and obtains required product.
Described promotor is dibutyl phthalate.
Described carbon felt refers to that Fibre diameter is 1 micron~800 microns, and staple length is more than or equal to 1 millimeter.
Low-resistance conductive plastic of the present invention adopts whole carbon felt as electrical conductor, has a large amount of macrofibers directly to be communicated with its tow sides in the carbon felt, mainly utilizes the carbon fiber on this direct conducting two sides to conduct electricity.Composite surface is carried out the vitriol oil handle, purpose is to remove the Resins, epoxy thin layer of clad surface carbon fiber, and the carbon fiber of conduction is directly come out, and reduces the contact resistance of plank and extraneous electrical conductor.Low-resistance conductive plastic of the present invention is at 128mA/cm 2Under the charge status, conductivity is good.Compare with graphite cake, can be by the electrolytic solution etching, the ability pile overcharges; Its physical strength height can enlarge the pole plate area, is used to equip high-power pile; Its production cost is low, and every material cost only is 1/3 of a graphite cake.
Embodiment
Embodiment 1
120 gram E51 bisphenol A-type liquid-state epoxy resins (the phoenix E51 of Wuxi resin processing plant), 60 gram 651 type polyamide resins (Wuxi resin processing plant) and 12 gram dibutyl phthalates are put in the hand baking oven baking to 80 ℃, and mixing stirs evenly.The carbon felt immersion of 150mm * 150mm * 6mm has been stirred in the mixture of Resins, epoxy and solidifying agent, noted to leave bubble in the carbon felt.Take out and flooded good carbon felt, place it in the tetrafluoroethylene mold slots of 100mm * 100mm * 6mm, add Resins, epoxy again to flush with groove, be covered with the pp plastic film, cover flat board, wait for being solidified into composition board with mixture to the liquid level of solidifying agent.Composition board after solidifying is taken out from mould, put into the groove that 80 ℃ of vitriol oils are housed, plate is fixed, make top and bottom can both fully contact the vitriol oil, open stirrer, stir the upper strata vitriol oil.After 30 minutes, it is fixing that composition board is turned over, and continues to stir 30 minutes.Open ultrasonic wave when stirring, make by the Resins, epoxy of vitriol oil carbonization to get off from surface desorption.Take out composition board, be placed in 85 ℃ the hot water ultrasonic cleaning 3 times, cleaned 5 minutes at every turn, and check the composite surface corrosive degree of depth and consistence.If depth of corrosion does not reach 1 millimeter, put into the groove that the vitriol oil is housed after the oven dry and continue to handle, up to reaching requirement.Clean then and dry, make required.
Embodiment 2
Place the baking oven baking to 50 ℃ in 400 gram 615A type Resins, epoxy (Wuxi resin processing plant), 100 gram 593 type solidifying agent (Wuxi resin processing plant), mix, stir evenly.The carbon felt of 318mm * 318mm * 6mm is put into the mould of 320mm * 320mm * 15mm groove, the Resins, epoxy that stirred and the mixture of solidifying agent are poured on the carbon felt, roll flatly with glass rod repeatedly, make the carbon felt can soak into mixture, attention can not leave bubble.Take out and flooded good carbon felt, place it on the plane that is covered with the PP plastic film, cover one deck PP plastic film above again, cover flat board, wait for being solidified into composition board.Composition board after solidifying is put into the groove that 80 ℃ of vitriol oils are housed, plate is fixed, make top and bottom can both fully contact the vitriol oil, open stirrer, stir the upper strata vitriol oil.After 30 minutes, it is fixing that composition board is turned over, and continues to stir 30 minutes.Take out composition board, be placed in 55 ℃ the hot water ultrasonic cleaning 3 times, cleaned 5 minutes at every turn, and check the composite surface corrosive degree of depth and consistence.If depth of corrosion does not reach 1 millimeter, put into the groove that the vitriol oil is housed after the oven dry and continue to handle, up to reaching requirement.Clean then and dry.
Embodiment 3
Place the baking oven baking to 40 ℃ in 2000 gram 615A type Resins, epoxy (Wuxi resin processing plant), 250 gram 593 type solidifying agent (Wuxi resin processing plant), mix, stir evenly.The carbon felt of 5 318mm * 318mm * 6mm is put into the mould of 320mm * 320mm * 75mm groove, the Resins, epoxy that stirred and the mixture of solidifying agent are poured on the carbon felt, and cover lid vacuumizes, make the carbon felt all soak into mixture, guarantee not stay bubble in the carbon felt.Take out and flooded good carbon felt, place it on the plane that is covered with the PP plastic film, cover one deck PP plastic film above again, cover flat board, wait for being solidified into composition board.Composition board after solidifying is put into the groove that 80 ℃ of vitriol oils are housed, composition board is fixed, make top and bottom can both fully contact the vitriol oil, open stirrer, stir the upper strata vitriol oil.After 30 minutes, it is fixing that composition board is turned over, and continues to stir 30 minutes.Take out composition board, be placed in 55 ℃ the hot water ultrasonic cleaning 3 times, cleaned 5 minutes at every turn, and check the composite surface corrosive degree of depth and consistence.If depth of corrosion does not reach 1 millimeter, put into the groove that the vitriol oil is housed after the oven dry and continue to handle, until reaching requirement.Clean then and dry.
Embodiment 4
With 2000 gram WHUT-RL70-A type Resins, epoxy (Wuhan nine dimension matrix material company limiteds), 1680 gram WHUT-RL-B type solidifying agent (Wuhan nine dimension matrix material company limiteds) and 20 gram WHUT-RL-C (promptly 2,4,6-three (dimethylamino methyl) phenol, Wuhan nine dimension matrix material company limiteds) place the baking oven baking to 70 ℃, mix, stir evenly.The carbon felt of 7 318mm * 318mm * 6mm is put into the mould of 320mm * 320mm * 75mm groove, the Resins, epoxy that stirred and the mixture of solidifying agent are poured on the carbon felt, and cover lid vacuumizes, make the carbon felt all soak into mixture, guarantee not stay bubble in the carbon felt.Take out and flooded good carbon felt, place it on the plane that is covered with the PP plastic film, cover one deck PP plastic film above again, cover flat board, wait for being solidified into composition board.Composition board after solidifying is put into the groove that 80 ℃ of vitriol oils are housed, plate is fixed, make top and bottom can both fully contact the vitriol oil, open stirrer, stir the upper strata vitriol oil.After 30 minutes, it is fixing that composition board is turned over, and continues to stir 30 minutes.Take out composition board, be placed in 55 ℃ the hot water ultrasonic cleaning 3 times, cleaned 5 minutes at every turn, and check the composite surface corrosive degree of depth and consistence.If depth of corrosion does not reach 1 millimeter, put into the groove that the vitriol oil is housed after the oven dry and continue to handle, until reaching requirement.Clean then and dry.
Embodiment 5
With 2000 gram WHUT-RL90-A type Resins, epoxy (Wuhan nine dimension matrix material company limiteds), 1440 gram WHUT-RL-B type solidifying agent (Wuhan nine dimension matrix material company limiteds) and 20 gram WHUT-RL-C (promptly 2,4,6-three (dimethylamino methyl) phenol, Wuhan nine dimension matrix material company limiteds) place the baking oven baking to 70 ℃, mix, stir evenly.The carbon felt of 7 318mm * 318mm * 6mm is put into the mould of 320mm * 320mm * 75mm groove, the Resins, epoxy that stirred and the mixture of solidifying agent are poured on the carbon felt, and cover lid vacuumizes, make the carbon felt all soak into mixture, guarantee not stay bubble in the carbon felt.Take out and flooded good carbon felt, place it on the plane that is covered with the PP plastic film, cover one deck PP plastic film above again, cover flat board, wait for being solidified into composition board.Composition board after solidifying is put into the groove that 80 ℃ of vitriol oils are housed, plate is fixed, make top and bottom can both fully contact the vitriol oil, open stirrer, stir the upper strata vitriol oil.After 30 minutes, it is fixing that composition board is turned over, and continues to stir 30 minutes.Take out composition board, be placed in 55 ℃ the hot water ultrasonic cleaning 3 times, cleaned 5 minutes at every turn, and check the composite surface corrosive degree of depth and consistence.If depth of corrosion does not reach 1 millimeter, put into the groove that the vitriol oil is housed after the oven dry and continue to handle, until reaching requirement.Clean then and dry.
Embodiment 6
Place the baking oven baking to 40 ℃ in 1000 gram WHUT-Esys 308A type Resins, epoxy (Wuhan nine dimension matrix material company limiteds), 1320 gram WHUT-Esys308B type solidifying agent (Wuhan nine dimension matrix material company limiteds), mix, stir evenly.The carbon felt of 7 318mm * 318mm * 6mm is put into the mould of 320mm * 320mm * 75mm groove, the Resins, epoxy that stirred and the mixture of solidifying agent are poured on the carbon felt, and cover lid vacuumizes, make the carbon felt all soak into mixture, guarantee not stay bubble in the carbon felt.Take out and flooded good carbon felt, place it on the plane that is covered with the PP plastic film, cover one deck PP plastic film above again, cover flat board, wait for being solidified into composition board.Composition board after solidifying is put into the groove that 80 ℃ of vitriol oils are housed, plate is fixed, make top and bottom can both fully contact the vitriol oil, open stirrer, stir the upper strata vitriol oil.After 30 minutes, it is fixing that composition board is turned over, and continues to stir 30 minutes.Take out composition board, be placed in 55 ℃ the hot water ultrasonic cleaning 3 times, cleaned 5 minutes at every turn, and check the composite surface corrosive degree of depth and consistence.If depth of corrosion does not reach 1 millimeter, put into the groove that the vitriol oil is housed after the oven dry and continue to handle, until reaching requirement.Clean then and dry.

Claims (2)

1. the preparation method of a low-resistance conductive plastic comprises the steps: successively
A) the raw materials quality per-cent prescription according to low-resistance conductive plastic quantitatively takes by weighing Resins, epoxy 30%~85%, solidifying agent 10%~60%, and promotor 0~3%, carbon felt 1%~55% is standby;
B) Resins, epoxy, solidifying agent and promotor are put into baking oven baking to 30 ℃~150 ℃, mix, stir evenly mixture A;
C) the carbon felt is immersed among the mixture A, makes and wherein do not stay bubble, take out and to put into mould, flatten, solidify composition board;
D) composition board after the above-mentioned curing is put into 20 ℃~150 ℃ the vitriol oil, stirred, adopt ultra-sonic oscillation to handle simultaneously 2 minutes to two hours;
E) take out composition board, put it in 50 ℃~90 ℃ the hot water, ultrasonic cleaning 3 times each 6 minutes, is dried moisture then;
Repeating step d) and step e) f), the composition board of oven dry moisture being dropped in the vitriol oil again, is 1 millimeter up to the surface corrosion degree of depth, cleans then and dries, and obtains required product.
2. low-resistance conductive plastic preparation method according to claim 1 is characterized in that: described promotor is dibutyl phthalate.
CN200910058605.5A 2009-03-11 2009-03-11 Preparation method of low-resistance conductive plastic Active CN101525468B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN200910058605.5A CN101525468B (en) 2009-03-11 2009-03-11 Preparation method of low-resistance conductive plastic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN200910058605.5A CN101525468B (en) 2009-03-11 2009-03-11 Preparation method of low-resistance conductive plastic

Publications (2)

Publication Number Publication Date
CN101525468A CN101525468A (en) 2009-09-09
CN101525468B true CN101525468B (en) 2011-06-22

Family

ID=41093546

Family Applications (1)

Application Number Title Priority Date Filing Date
CN200910058605.5A Active CN101525468B (en) 2009-03-11 2009-03-11 Preparation method of low-resistance conductive plastic

Country Status (1)

Country Link
CN (1) CN101525468B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103367764A (en) * 2011-05-25 2013-10-23 深圳市金钒能源科技有限公司 Composite conductive electrode and manufacturing method thereof
CN102637881B (en) * 2012-04-11 2015-03-25 朝阳华鼎储能技术有限公司 Method for preparing electroconductive plastic bipolar plate for vanadium cell
CN103035928B (en) * 2012-12-18 2015-04-15 中国科学院金属研究所 Integrated electrode for vanadium cell and preparation method thereof
CN109216709A (en) * 2017-06-29 2019-01-15 中国科学院金属研究所 A kind of dig pit effect construction method and its application of high-ratio surface carbon fiber felt
CN111525150A (en) * 2020-05-09 2020-08-11 乐山创新储能技术研究院有限公司 Preparation method of flow battery composite electrode

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101163828A (en) * 2005-04-19 2008-04-16 帝人株式会社 Carbon fiber composite sheet, use of the same as heat transferring article, and sheet for pitch-based carbon fiber mat for use therein

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101163828A (en) * 2005-04-19 2008-04-16 帝人株式会社 Carbon fiber composite sheet, use of the same as heat transferring article, and sheet for pitch-based carbon fiber mat for use therein

Also Published As

Publication number Publication date
CN101525468A (en) 2009-09-09

Similar Documents

Publication Publication Date Title
CN101525468B (en) Preparation method of low-resistance conductive plastic
CN102891324B (en) Bipolar plate for vanadium battery and preparation method for bipolar plate
AU2006239017B2 (en) Electrode and manufacturing methods
CN103219532B (en) Flow battery sulfonated polyether-ether-ketone base blend ion exchange membrane and preparation method thereof
CN101698945B (en) Carbon-fiber reinforced cathode carbon block and preparation method thereof
CN102891335A (en) Preparation method of full-solid-state nano composite polymer electrolyte
CN107046140A (en) A kind of fluorine-containing bipolar plates and preparation method thereof
CN1880375A (en) Polymer electrolyte and fuel cell using the same
CN109755043A (en) Self-healing integration gel state supercapacitor and preparation method thereof
CN106191967B (en) A kind of process of the doped graphene in polypyrrole coating
CN1927921A (en) Lithium ion conducting gel film containing porous polymer framework and preparation method thereof
JP2014207122A (en) Bipolar plate and process of manufacturing the same
CN109904411A (en) A kind of preparation method and application of negative electrode of lithium ion battery graphite and cobalt-based metal organic frame composite material
CN103165921B (en) Fuel cell separator plate and comprise the fuel cell of this dividing plate
CN111934028B (en) Lead-acid battery manufacturing method based on conductive adhesive and lead sulfate
CN103013408A (en) Preparation method of conductive adhesive cured at room temperature
CN111525150A (en) Preparation method of flow battery composite electrode
CN111525149A (en) Preparation method of flow battery composite electrode
CN105047939B (en) A kind of lead-acid battery is with modified short fine preparation method and includes the short fine negative plate of the modification
CN107742696A (en) A kind of preparation method for lead charcoal negative pole charcoal based additive
CN108165007A (en) The preparation method of high heat conductive insulating baseplate material that a kind of PCB is filled with graphene coated copper powder
CN106328954B (en) Vanadium redox battery current collector and preparation method thereof
CN101928962A (en) Method for plasticizing anode paste
CN101922021A (en) Anode paste and carbon anode made from same
CN1924102A (en) Preparation method of lead dioxide porous electrode

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
ASS Succession or assignment of patent right

Owner name: CHONGQING ZHONGWU ENERGY TECHNOLOGY CO., LTD.

Free format text: FORMER OWNER: ELECTRONICS ENGINEERING INST., CHINA ENGINEERING PHYSICS RESEARCH ACADEMY

Effective date: 20140603

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 621900 MIANYANG, SICHUAN PROVINCE TO: 400700 BEIPEI, CHONGQING

TR01 Transfer of patent right

Effective date of registration: 20140603

Address after: 400700 Chongqing District of Beibei City, the town of salt dam No. 1

Patentee after: Chongqing Zhong Ye Energy Technology Co.,Ltd.

Address before: 919 box 516, box 621900, Mianyang City, Sichuan Province

Patentee before: INSTITUTE OF ELECTRONIC ENGINEERING,China Academy of Engineering Physics

C56 Change in the name or address of the patentee

Owner name: MIANYANG ZHONGWU ENERGY TECHNOLOGY CO., LTD.

Free format text: FORMER NAME: CHONGQING ZHONGWU ENERGY TECHNOLOGY CO., LTD.

CP03 Change of name, title or address

Address after: Mianyang City, Sichuan Province, 621900 Mountain Road No. 64 (city of science five civilian area six floor)

Patentee after: Mianyang Zhongwu Energy Technology Co.,Ltd.

Address before: 400700 Chongqing District of Beibei City, the town of salt dam No. 1

Patentee before: Chongqing Zhong Ye Energy Technology Co.,Ltd.

TR01 Transfer of patent right

Effective date of registration: 20220928

Address after: 621000 No.64-5, Mianshan Road, Youxian District, Mianyang City, Sichuan Province

Patentee after: Sichuan Huantong Electronics Co.,Ltd.

Address before: 621900 No.64 Mianshan Road, Mianyang City, Sichuan Province

Patentee before: Mianyang Zhongwu Energy Technology Co.,Ltd.

TR01 Transfer of patent right