CN107201508A - The method for lifting the hydrophily and electric conductivity of carbon cloth - Google Patents

The method for lifting the hydrophily and electric conductivity of carbon cloth Download PDF

Info

Publication number
CN107201508A
CN107201508A CN201610150125.1A CN201610150125A CN107201508A CN 107201508 A CN107201508 A CN 107201508A CN 201610150125 A CN201610150125 A CN 201610150125A CN 107201508 A CN107201508 A CN 107201508A
Authority
CN
China
Prior art keywords
plasma
carbon cloth
hydrophily
electric conductivity
lifting
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.)
Pending
Application number
CN201610150125.1A
Other languages
Chinese (zh)
Inventor
邱国峰
吕晃志
陈亭竹
柯绍仁
谢丰州
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.)
SHENHU BATTERIES CO Ltd TAIWAN PROV
CSB Energy Technology Co Ltd
Original Assignee
SHENHU BATTERIES CO Ltd TAIWAN PROV
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 SHENHU BATTERIES CO Ltd TAIWAN PROV filed Critical SHENHU BATTERIES CO Ltd TAIWAN PROV
Priority to CN201610150125.1A priority Critical patent/CN107201508A/en
Publication of CN107201508A publication Critical patent/CN107201508A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/50Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges
    • C23C16/513Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges using plasma jets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/403Manufacturing processes of separators, membranes or diaphragms
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409Separators, membranes or diaphragms characterised by the material
    • H01M50/431Inorganic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409Separators, membranes or diaphragms characterised by the material
    • H01M50/44Fibrous material
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Electrochemistry (AREA)
  • Plasma & Fusion (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Inert Electrodes (AREA)

Abstract

A kind of method for the hydrophily and electric conductivity for lifting carbon cloth, is comprised the steps of:Plasma-based processing is bestowed to a carbon cloth, react the carbon cloth and a hydroaropic substance and in forming hydrophilic functional group group on the carbon cloth, and carbon fiber in the carbon cloth is broken and is formed loose structure, and the carbon cloth handled through plasma-based after hydrophily and electric conductivity be more than the hydrophily and electric conductivity of the carbon cloth plasma-based before processing.Methods described can lift the hydrophily and electric conductivity of carbon cloth.

Description

The method for lifting the hydrophily and electric conductivity of carbon cloth
Technical field
The present invention relates to a kind of method for the hydrophily and electric conductivity for lifting carbon cloth, it is particularly It is related to a kind of method that the hydrophily and electric conductivity that lift carbon cloth are handled by plasma-based.
Background technology
TaiWan, China patent I318243 discloses a kind of preparation method of hydrophobicity carbonaceous material, be in order to Obtain the gas diffusion layers of a membrane electrode and further apply in fuel cell, so Activated carbon fiber is modified using plasma-based, to increase its hydrophobicity.The work modified through plasma-based Property carbon fiber has excellent hydrophobicity, and good porous supplied gas can be maintained to spread, can Effectively improve the power output of fuel cell.
However, the application of the hydrophobicity carbonaceous material is limited, it is impossible to suitable for various fields, For for example with plumbic acid capacitance field of batteries, because the electrode of plumbic acid capacitance battery is direct and sulfuric acid Electrolyte contacts, so the hydrophobicity carbonaceous material is not appropriate for applying in lead-acid battery electric capacity In.
Based on above-mentioned, it is still necessary to proposing a kind of method for modifying of novel carbon cloth.
The content of the invention
The purpose of the present invention is to be to provide a kind of hydrophily and electric conductivity for lifting carbon cloth Method.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, is comprised the steps of:
Plasma-based processing is bestowed to a carbon cloth, makes the carbon cloth and a hydrophily thing Qualitative response and in forming hydrophilic functional group group on the carbon cloth, and make the carbon fine Carbon fiber in dimension cloth is broken and forms loose structure, and the carbon cloth is handled through plasma-based Hydrophily and electric conductivity afterwards is more than the hydrophily and conduction of the carbon cloth plasma-based before processing Property.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, also comprising one in institute State the heat treatment after plasma-based processing.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, the heat treatment Temperature range is 120 to 170 DEG C.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, the plasma-based processing Unit interval processing area scope to the carbon cloth is 222mm2/ sec to 318 mm2/sec。
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, the plasma-based processing Unit area processing power amount scope to carbon cloth is 3.18W/mm2To 63.6W/mm2
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, when the progress electricity During slurry processing, the temperature range that the plasma-based handles the surface for causing the carbon cloth is 50 To 90 DEG C.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, the hydrophily thing Matter is oxygen containing material.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, the oxygen containing thing Matter is derived from air, oxygen plasma, or these combinations.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, the plasma-based processing Plasma-based be selected from nitrogen plasma-based, oxygen plasma, helium plasma-based, argon gas plasma-based, or on The combination stated.
The method of the hydrophily and electric conductivity of present invention lifting carbon cloth, the plasma-based processing Power bracket be 50 watts to 700 watts.
The beneficial effect of the present invention is:Being handled by the plasma-based makes the carbon cloth With hydroaropic substance reaction in formation hydrophilic functional group group on the carbon cloth,
Therefore the hydrophily of the carbon cloth is lifted, and the carbon is made by plasma-based processing Carbon fiber in fiber cloth is broken and forms loose structure, therefore the lifting carbon cloth Electric conductivity.
Brief description of the drawings
Fig. 1 is embodiment 1 to 4 in nitrogen (N2) fourier transform infrared spectroscopy figure under environment;
Fig. 2 is fourier transform infrared spectroscopy figure of the embodiment 1 to 4 under atmospheric environment;
Fig. 3 is embodiment 1 and the button cell charge-discharge test result of comparative example 1, is It is 1.5mA/cm in charging and discharging currents density2When a specific capacitance to the pass of charging and discharging currents density System's figure;
Fig. 4 is the photo of the sweep electron microscope of embodiment 1;
Fig. 5 is the photo of the sweep electron microscope of embodiment 2;
Fig. 6 is the photo of the sweep electron microscope of embodiment 3;And
Fig. 7 is the photo of the sweep electron microscope of embodiment 4.
Embodiment
It will be described in detail below with regard to present invention:
In this article, the hydrophilic functional group group is such as, but not limited to:C=O, O-C-O, COOH, OH etc..There is no particular restriction for the species of the carbon cloth, as long as can make carbon after being handled through plasma-based Most carbon fibers in fiber cloth are activated and with hydroaropic substance reaction in the carbon Hydrophilic functional group group is connected on fiber, and handle through plasma-based can make the carbon fiber be broken and The carbon cloth for producing loose structure is all applicable.Preferably, the carbon cloth is that activated carbon is fine Wei Bu (activated carbon fiber).There is no particular restriction for the hydroaropic substance, only It can be reacted with the carbon fiber being activated in carbon cloth after plasma-based processing and form hydrophily official The hydroaropic substance of energy group is all applicable.It is preferred that the hydroaropic substance is oxygen containing material. It is preferred that the oxygen containing material is derived from air, oxygen plasma, or an above-mentioned combination.
It is preferred that the plasma-based is processed as atmospheric pressure plasma processing, handled using the atmospheric pressure plasma When, control operation condition is relatively easy to, and contribute to the carbon cloth of large area to carry out at plasma-based Reason.It is preferred that the plasma-based of the plasma-based processing is to be selected from nitrogen plasma-based, oxygen plasma, helium Pneumoelectric slurry, argon gas plasma-based, or these combinations.The conditional parameter of the plasma-based processing, for example There is no particular restriction for power bracket, flow rates, rate travel and operating distance etc., as long as energy Make to form hydrophilic functional group group on the carbon cloth and the carbon fiber is broken and is produced Raw loose structure.It is preferred that the power bracket of the plasma-based processing is 50 watts to 700 Watt, it can more lift hydrophily and electric conductivity after the carbon cloth is handled through plasma-based.Preferably Ground, the plasma-based processing is 222 to the unit interval processing area scope of the carbon cloth mm2/ sec to 318mm2/ sec, can more lift the parent after the carbon cloth is handled through plasma-based Aqueous and electric conductivity.It is preferred that the plasma-based processing handles work(to the unit area of carbon cloth Rate amount scope is 3.18W/mm2To 63.6W/mm2, the carbon cloth can be more lifted through electricity Hydrophily and electric conductivity after slurry processing.It is preferred that when carrying out the plasma-based processing, it is described The temperature range that plasma-based handles the surface for causing the carbon cloth is 50 to 90 DEG C, Neng Gougeng Lift hydrophily and electric conductivity after the carbon cloth is handled through plasma-based.The plasma-based processing Plasma-based flow rates are such as, but not limited to 5 to 70ml/min.The working distance of the plasma-based processing It is 5 to 25mm from scope.The plasma-based rate travel scope of plasma-based processing for example but is not limited In 1 to 700mm/s.
It is preferred that it is described lifting carbon cloth hydrophily and electric conductivity method also comprising one Heat treatment after the plasma-based processing.It can be made after being handled through the plasma-based by the heat treatment The carbon cloth there is long-acting electric conductivity.The operating environment of the heat treatment has no especially Limitation, can be in or be not in vacuum or particular atmosphere and carry out.It is preferred that the temperature of the heat treatment It is 120 to 170 DEG C to spend scope.When the temperature range of the heat treatment is 120 to 170 DEG C, It can cause the carbon cloth after being handled through the plasma-based that there is more efficient electric conductivity.It is described The time of heat treatment, there is no particular restriction, such as, but not limited to 2 to 3 hours.
Compared to the carbon cloth handled without the plasma-based, the carbon handled by the plasma-based is fine Wei Bu has higher hydrophily and electric conductivity, and its application field is such as, but not limited to plumbic acid capacitance Battery.When the carbon cloth handled through plasma-based is applied in plumbic acid capacitance battery, because through plasma-based Carbon fiber in the carbon cloth of processing is broken and forms loose structure so being led with higher Electrically, and the electric charge in more electrolyte can be adsorbed, and because the carbon handled through plasma-based Hydrophilic functional group group is formed with fiber cloth and electrolyte is more moistened into carbon cloth In, so that plumbic acid capacitance battery has higher capacitance.
The present invention will be further illustrated with regard to following examples, however, it should be noted that described implement Example is only to illustrate, and is not necessarily to be construed as the limitation that the present invention is implemented.
[embodiment 1]
Plasma-based processing:By an activated carbon fiber cloth (manufacturer:Tai Tan Science and Technology Co., Ltd., Model:AW-1114, average specific surface area is 1100m2/ g, size be 1030 × 1000 × 0.4mm3), with a normal pressure nitrogen plasma-based device [pen type (pen-l ike), nitrogen gas purity 99.99%] Plasma-based processing, and the control moved using energy X-Y bis- axles are bestowed to the activated carbon fiber cloth Device processed manipulates the movement of the normal pressure nitrogen plasma-based device.The activated carbon fiber cloth is kept flat After on the platform of the control device, first make the nitrogen plasma-based of the normal pressure nitrogen plasma-based device Along the inswept activated carbon fiber cloth of the weft direction of the activated carbon fiber cloth once, it is then suitable The inswept activated carbon fiber cloth of warp direction for the activated carbon fiber cloth once, is done with this For the scanning number of turns " 1 circle ", (unit area processing power amount when " 1 circle " is 3.18W/mm2, Often increase by one is enclosed, and unit area processing power amount is to increase one times.).Wherein, at the plasma-based The power of reason is 100 watts, and the flow velocity of the nitrogen plasma-based is 15ml/min, the nitrogen electricity A diameter of 4mm of slurry effect, the operating distance between nitrogen plasma-based and the activated carbon fiber cloth is 1.5cm, the rate travel of the normal pressure nitrogen plasma-based device is 30mm/s.
Heat treatment:Then, the activated carbon fiber cloth handled through plasma-based is placed on a stainless steel disc On, it is placed into a circulation baking oven, by the temperature control of the circulation baking oven at 150 DEG C, heat Processing 2 hours, is obtained once upgrading activity carbon cloth.
[embodiment 2 to 4]
In embodiment 2 to 4 plasma-based processing and heat treatment mode be it is in the same manner as in Example 1, Difference is the number of turns for changing plasma-based processing.In embodiment 1 to 4 plasma-based handle the number of turns be as Shown in table 1.
[comparative example 1]
With commercially available and not modified activated carbon fiber cloth (manufacturer:The limited public affairs of platform carbon science and technology share Department, model:AW-1114, average specific surface area is 1100 meters squared per grams) as comparative example 1.
[application of modified activated carbon fiber cloth] button type rechargeable battery
Prepared respectively according to existing mode using the modified activated carbon fiber cloth of embodiment 1 and 2 Into CR2032 button cells, wherein, the structure of button type rechargeable battery is from the bottom to top sequentially For:Stainless steel lower cover, stainless steel substrates, high-hydrophilic conductive carbon fibre cloth, PP barrier films, height Conductive hydrophilic carbon cloth, spring leaf, and stainless steel upper cover, and using concentration as 1M H2SO4 As electrolyte.
And be prepared into using comparative example 1 without upgrading activity carbon cloth according to identical mode CR2032 button cells.
[assessment item]
1. water contact angle
The modified activated carbon for measuring embodiment 1 to 4 using sessile drop method (Sessile Drop) is fine Wei Bu, and water contact angle of the comparative example 1 without upgrading activity carbon cloth.Water contact angle As a result it is as shown in table 1.
2.X- ray photoelectron spectroscopics (XPS)
With X-ray photoelectron spectrograph (manufacturer:ULVAC-PHI, model:PHI 5000 Versaprobe II) the modified activated carbon fiber cloth of embodiment 1 to 4 is measured, and compare Example 1 is without upgrading activity carbon cloth.The result of the X-ray photoelectron spectroscopy such as institute of table 2 and 3 Show.
3. fourier transform infrared spectroscopy (FTIR)
With Fourier transform infrared spectrum analysis instrument (manufacturer:Thermo Scientific, type Number:Nicilet 6700) measure embodiment 1 to 4 modified activated carbon fiber cloth.Fu Li The result of leaf transform infrared spectroscopy is as shown in Figures 1 and 2.
4. AC impedance spectrum measurement (EIS)
By the button cell obtained by above-mentioned use embodiment 1 and comparative example 1, with constant potential Instrument (manufacturer:Autolab, model:PGSTAT30 AC impedance spectrum measurement) is carried out, is obtained The interracial contact impedance (Rc) of button cell obtained by embodiment 1 and comparative example 1, as a result As shown in table 1.
5. charge-discharge test
With potentiostat (manufacturer:Autolab, model:PGSTAT30) implementation is used to above-mentioned Button cell obtained by example 1,2 and comparative example 1 carries out charge-discharge test.Wherein, exist Charging and discharging currents density is 1.5mA/cm2When, the button type of embodiment 1,2 and comparative example 1 The specific capacitance value result of battery is as shown in table 1, the button type electricity of embodiment 1 and comparative example 1 The specific capacitance in pond is as shown in Figure 3 to the graph of a relation of charging and discharging currents density.
Table 1
Note:" --- " represents not measure.
Table 2
Table 3
[note]:
I(a):Aqueous vapor adsorbs (adsorbed water);
II(a):Oxygen atom in C-O, hydroxyl;
III(a):The oxygen in C=O, carboxyl, quinone (quinone) in carbonyl;
I(b):The carbon of carboxyl and ester group;
II(b):The carbon of carbonyl, quinonyl and ketone group;
III(b):The carbon of alcohol radical and ether;
IV(b):Graphite;
V(b):Carbide (carbide).
From table 1 it was found from the result of water contact angle, the modified activated carbon of embodiment 1 to 4 is fine The water contact angle for tieing up cloth is 0 degree, represents the modified activated carbon fiber cloth tool of embodiment 1 to 4 There is very high hydrophily.Water contact angle of the comparative example 1 without upgrading activity carbon cloth is 120 Degree, represents hydrophily of the embodiment 1 without upgrading activity carbon cloth poor.Prove by electricity Slurry processing can cause really carbon cloth handled through plasma-based after hydrophily be more than carbon cloth electricity Starch the hydrophily of before processing.
From table 2 it was found from the result of " O1s " peak value, the modified activity of embodiment 1 to 4 The relative amount of the oxygen of carbon cloth is 22.4% to 34.6%, and comparative example 1 is not modified The relative amount of the oxygen of activated carbon fiber cloth is 11.3%, it was demonstrated that being handled by plasma-based can make really Most carbon fibers in carbon cloth are obtained to be activated and react and cause on carbon cloth with oxygen Oxygen increase.And coordinate Fig. 1 and 2 to understand, the modified activated carbon fiber cloth tool of embodiment 1 to 4 There is hydrophilic functional group (O-H, C=O, C-O ,-COOH), it was demonstrated that handle true by the plasma-based It is real can cause most carbon fibers in carbon cloth be activated and with hydroaropic substance reaction in Hydrophilic functional group group is connected on the carbon fiber.
" I (a) of O1s peak positions " relative amount in table 2 and table 3 is coordinated to understand, embodiment The relative amount that 1 modified activated carbon fiber cloth adsorbs aqueous vapor is 3.36% (0.15 × 0.224 × 100%), the modified activated carbon fiber cloth of embodiment 2 adsorbs water The relative amount of gas is 5.88% (0.17 × 0.346 × 100%), the modified activated carbon of embodiment 3 The relative amount that fiber cloth adsorbs aqueous vapor is 9.74% (0.29 × 0.336 × 100%), embodiment The relative amount that 4 modified activated carbon fiber cloths adsorb aqueous vapor is 9.95% (0.32 × 0.311 × 100%), all higher than comparative example 1 without upgrading activity carbon cloth The relative amount of adsorbed aqueous vapor is 1.58% (0.14 × 0.113 × 100%), it was demonstrated that pass through plasma-based Processing can cause really carbon cloth handled through plasma-based after hydrophily be more than the carbon cloth The hydrophily of plasma-based before processing.
From the result of the median surface contact impedance of table 1, the button type electricity obtained by embodiment 1 Pond has relatively low interracial contact impedance, and the button cell obtained by comparative example 1 has higher Interracial contact impedance.And in table 1 charge-discharge test result, embodiment 1 with Button cell obtained by embodiment 2 can bear faster charge rate, and comparative example 1 is made The button type electricity obtained can only bear slower charge rate.And from the figure 3, it may be seen that the institute of embodiment 1 Obtained button cell has higher specific capacitance, and button cell made from comparative example 1 has There is relatively low specific capacitance.Proving to handle by the plasma-based can cause carbon cloth through plasma-based really Electric conductivity after processing is more than the electric conductivity of the carbon cloth plasma-based before processing, so that Button cell has preferably performance.
Proved by Fig. 4 to 7, handled by plasma-based and cause the carbon fiber in carbon cloth to break really Split and form loose structure.
In summary, the carbon cloth and the hydrophily thing can be made by being handled by the plasma-based Qualitative response and in forming hydrophilic functional group group on the carbon cloth, therefore it is fine to lift the carbon The hydrophily of cloth is tieed up, and being handled by the plasma-based makes the carbon fiber in the carbon cloth break Split and form loose structure, therefore the electric conductivity of the lifting carbon cloth, therefore can reach really The purpose of the present invention.
It is simply described above, be presently preferred embodiments of the present invention, when can not use this limit this Invent the scope implemented, that is to say, that generally according to claims of the present invention and description of the invention institute The simple equivalent changes and modifications made, all still belongs to the scope that the present invention covers.

Claims (10)

1. a kind of method for the hydrophily and electric conductivity for lifting carbon cloth, it is characterised in that It is comprised the steps of:
Plasma-based processing is bestowed to a carbon cloth, makes the carbon cloth and a hydrophily thing Qualitative response and in forming hydrophilic functional group group on the carbon cloth, and make the carbon fine Carbon fiber in dimension cloth is broken and forms loose structure, and the carbon cloth is handled through plasma-based Hydrophily and electric conductivity afterwards is more than the hydrophily and conduction of the carbon cloth plasma-based before processing Property.
2. the hydrophily and electric conductivity of lifting carbon cloth according to claim 1 Method, it is characterised in that:It is also comprising the heat treatment one after plasma-based processing.
3. the hydrophily and electric conductivity of lifting carbon cloth according to claim 2 Method, it is characterised in that:The temperature range of the heat treatment is 120 to 170 DEG C.
4. the hydrophily and electric conductivity of lifting carbon cloth according to claim 1 Method, it is characterised in that:The plasma-based processing was handled the unit interval of the carbon cloth Areal extent is 222mm2/ sec to 318mm2/sec。
5. the hydrophily and electric conductivity of lifting carbon cloth according to claim 1 Method, it is characterised in that:Unit area processing power of the plasma-based processing to carbon cloth Amount scope is 3.18W/mm2To 63.6W/mm2
6. the hydrophily and electric conductivity of lifting carbon cloth according to claim 1 Method, it is characterised in that:When carrying out the plasma-based processing, the plasma-based, which is handled, causes institute The temperature range for stating the surface of carbon cloth is 50 to 90 DEG C.
7. the hydrophily and electric conductivity of lifting carbon cloth according to claim 1 Method, it is characterised in that:The hydroaropic substance is oxygen containing material.
8. the hydrophily and electric conductivity of lifting carbon cloth according to claim 7 Method, it is characterised in that:The oxygen containing material is derived from air, oxygen plasma, or One is combined.
9. the hydrophily and electric conductivity of lifting carbon cloth according to claim 1 Method, it is characterised in that:The plasma-based of the plasma-based processing is to be selected from nitrogen plasma-based, oxygen Plasma-based, helium plasma-based, argon gas plasma-based, or an above-mentioned combination.
10. the hydrophily and electric conductivity of lifting carbon cloth according to claim 1 Method, it is characterised in that:The power bracket of the plasma-based processing is 50 watts to 700 watts.
CN201610150125.1A 2016-03-16 2016-03-16 The method for lifting the hydrophily and electric conductivity of carbon cloth Pending CN107201508A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610150125.1A CN107201508A (en) 2016-03-16 2016-03-16 The method for lifting the hydrophily and electric conductivity of carbon cloth

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610150125.1A CN107201508A (en) 2016-03-16 2016-03-16 The method for lifting the hydrophily and electric conductivity of carbon cloth

Publications (1)

Publication Number Publication Date
CN107201508A true CN107201508A (en) 2017-09-26

Family

ID=59903817

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610150125.1A Pending CN107201508A (en) 2016-03-16 2016-03-16 The method for lifting the hydrophily and electric conductivity of carbon cloth

Country Status (1)

Country Link
CN (1) CN107201508A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109806824A (en) * 2019-03-25 2019-05-28 南京工业大学 A kind of extensive, the quickly hydrophilic microwave method of improvement carbon substrate and its application

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5376413A (en) * 1990-08-22 1994-12-27 Sommer Societe Anonyme Treatment of textile fibers
CN1436889A (en) * 2002-02-04 2003-08-20 中国科学院化学研究所 Production process of conductive fabric via plasma treatment
CN101265659A (en) * 2008-04-03 2008-09-17 武汉科技学院 Method for plasma spray gun improving textile material hydrophilicity
CN102444021A (en) * 2011-08-22 2012-05-09 翔瑞(泉州)纳米科技有限公司 Intelligent waterproof and moisture permeable fabric
CN102723502A (en) * 2011-06-01 2012-10-10 中国科学院金属研究所 Surface modification method for raising activity of electrode material of vanadium cell

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5376413A (en) * 1990-08-22 1994-12-27 Sommer Societe Anonyme Treatment of textile fibers
CN1436889A (en) * 2002-02-04 2003-08-20 中国科学院化学研究所 Production process of conductive fabric via plasma treatment
CN101265659A (en) * 2008-04-03 2008-09-17 武汉科技学院 Method for plasma spray gun improving textile material hydrophilicity
CN102723502A (en) * 2011-06-01 2012-10-10 中国科学院金属研究所 Surface modification method for raising activity of electrode material of vanadium cell
CN102444021A (en) * 2011-08-22 2012-05-09 翔瑞(泉州)纳米科技有限公司 Intelligent waterproof and moisture permeable fabric

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109806824A (en) * 2019-03-25 2019-05-28 南京工业大学 A kind of extensive, the quickly hydrophilic microwave method of improvement carbon substrate and its application

Similar Documents

Publication Publication Date Title
Zhang et al. Single Fe atom on hierarchically porous S, N‐codoped nanocarbon derived from porphyra enable boosted oxygen catalysis for rechargeable Zn‐air batteries
Zhang et al. Highly wettable and metallic NiFe-phosphate/phosphide catalyst synthesized by plasma for highly efficient oxygen evolution reaction
He et al. Carbon layer-exfoliated, wettability-enhanced, SO3H-functionalized carbon paper: A superior positive electrode for vanadium redox flow battery
CN105826572B (en) A kind of N, S codope carbon nanotube coat FexC catalyst, preparation method and applications
CN110492081A (en) A kind of preparation method and applications of cobaltous selenide/porous carbon nanotube of zinc selenide N doping
Hsieh et al. Fabrication of flower-like platinum clusters onto graphene sheets by pulse electrochemical deposition
CN106532074B (en) A kind of preparation method of nanometer cobalt/graphene nucleocapsid elctro-catalyst
Wang et al. Carbon riveted PtRu/C catalyst from glucose in-situ carbonization through hydrothermal method for direct methanol fuel cell
CN110067003A (en) Monatomic doped graphene material of metal and the preparation method and application thereof
Zha et al. Coconut shell carbon nanosheets facilitating electron transfer for highly efficient visible-light-driven photocatalytic hydrogen production from water
Thomas et al. Carbon nanotubes as catalyst supports for ethanol oxidation
CN103007926A (en) Preparation method of platinum/vertical graphene composite material electrocatalyst
CN113881965B (en) Metal nanoparticle supported catalyst with biomass carbon source as template and preparation method and application thereof
Liu et al. Synergistic effects of niobium oxide–niobium carbide–reduced graphene oxide modified electrode for vanadium redox flow battery
CN106206051B (en) A kind of graphene modified activated carbon and its application
CN116111109A (en) Carbon electrode composite material, preparation method thereof and secondary battery
CN107910560A (en) Nano carbon-base N doping base metal composite electro catalytic material and its preparation method using high annealing and application
CN102610809B (en) Ferroferric oxide/graphite lithium ion battery anode material and preparation method for ferroferric oxide/graphite lithium ion battery anode material
CN109709187A (en) A kind of carbon fiber and the preparation method and application thereof
CN104084193A (en) Method for preparing Pt catalyst
Lai et al. Comparison between atmospheric-pressure-plasma-jet-processed and furnace-calcined rGO-MnOx nanocomposite electrodes for gel-electrolyte supercapacitors
CN107201508A (en) The method for lifting the hydrophily and electric conductivity of carbon cloth
CN105529194B (en) A kind of MnO2@graphene capsule@MnO2The preparation method of composite
CN102698741A (en) Method for preparing grapheme platinum nanocomposite material by using argon plasma
Li et al. Electrochemical behavior of diverse vanadium ions at modified graphite felt electrode in sulphuric solution

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20170926