CN1169443A - Method for preparing high electric-activity conductive bending-resistant nanometre compound film - Google Patents
Method for preparing high electric-activity conductive bending-resistant nanometre compound film Download PDFInfo
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- CN1169443A CN1169443A CN 96108338 CN96108338A CN1169443A CN 1169443 A CN1169443 A CN 1169443A CN 96108338 CN96108338 CN 96108338 CN 96108338 A CN96108338 A CN 96108338A CN 1169443 A CN1169443 A CN 1169443A
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Abstract
The present invention relates to a structure controllable forming method for directly preparing high electric activity, conductive and folding-proof nanometer composite membrane by using organic disulfide, mercaptothiazole and their derivatives and performed polymer, bisphenol A and epoxy resin as raw-material monomet. Said invention uses the regulation of such conditions of medium, monomer and performed polymer concentrations, electric field and magnetic field intensities, reaction time and environmental temp. to control product structure to make nanomet4r composite membrane. Said invented composite membrane can be used for makin gthin-film high-energy secondary cell electrode, electrolyte, high-conductive electromagnetic shielding packaging film with folding strength and resistance to mechanical deformation, oi-proof conductive sealing part, corrosion-proofing coating and medical sensor non-toxic probe film etc..
Description
The present invention relates to the preparation method of nano composite membrane, specifically be meant to be applied to energy environment protection, information sensing technology, biology---the preparation method of the high electric-activity conductive bending-resistant nanometre compound film in field such as medicine equipment, chemical separating are anticorrosion, automobile, electromagnetic interference shield and electrostatic dissipation.
Because high electroactive conductive bending-resistant thin film application is increasingly extensive, its research is received various countries scientist's concern, also produced the new results of many this respects.Organic disulfide/conductive polymers (as polyaniline) mixture as the high energy electrode for secondary battery.Though potentiality are very big, but still have oxidation---the reduction potential difference higher (～0.5V), promptly reversibility is little, the charging and discharging currents density difference is big, causes in the charge and discharge cycles energy consumption big; This mixture forms electrode by organic disulfide and two kinds of powder mixes compactings of polyaniline, and itself does not have flexibility, whole easily embrittlement in mechanical deformation, collision vibrations; Support with flexible carrier, even the solid gel ionogen, the adding volume ratio that has reaches more than 50%, has both reduced energy density, has increased the transmission resistance and the operation such as gluing at carrier and electrode materials interface again, increase electrode performance labile factor.Comprising under mechanical effects such as distortion, vibrations, electric conductivity, electroactive conservation rate etc.
In addition, mix a large amount of H in the industrial gaseous waste
2S, SO
2, etchant gas, dust such as sulfurous acid, fail high-efficiency low energy consumption separates, reclaims always; The detection of sulfydryl and disulfide linkage and catalyzed degradation are poisonous and hard with inorganic materials such as traditional method such as silver chloride work probe in the protein, are unsuitable for the energy-conservation degraded of biotechnology of medical-therapeutic treatment of human body or hair; The galvanic corrosion of metal such as steel is serious under the high oxidation condition, as the protection of rocket pod and the sealing corrosion of oil resistant spare etc., all do not obtain effective material that can address the above problem.Therefore, material becomes the focus of domestic and international joint research.Chinese patent application number: 92105905.1 start a kind of method of directly being made intrinsic conducting polymer (ICP) fento, film, thick product by starting monomer, it had both solved the contradiction of goods high-performance and moulding difficulty, greatly reduce raw material and energy expenditure again, avoid taking place in the production process contaminate environment simultaneously.But,, further improve the multifunctional performance of composite product for opening up purposes widely.
The objective of the invention is to, overcome the weak point of above-mentioned background technology, on the basis of continuing to use the controlled architecture reaction method of forming, provide a kind of by two classes or/and the above starting monomer of two classes directly prepares the method for high electroactive, conduction, folding nano composite membrane.It utilizes two classes or/and the synergistic effect of the above starting monomer of two classes further improves product properties, when goods use as electrode for secondary battery, and oxidation---reduction potential is poor＜0.05V, and in 50mV/S rose to the 100mV/S scope, this difference remained unchanged; Products thickness can be as thin as＜20 μ m, can directly make the shape and size of service requirements, and good with adhibit qualities such as metals such as steel, aluminium, copper or polymer solid electrolyte films; Electric conductivity is up to the film more than the 100S/cm, folding 180 ° 50 times (more than) after not only kept flexible but also keep electric conductivity～75%; Prepare the sensitive membrane that is fit to human medical detection requirement, sulfydryl or disulfide bond content are little to 10
-5～10
-7In the mol/L scope, can reflect the linear change of micro voltage (electric current); Goods can also be used for absorption, separation, protein degradation, and electric field action is absorption inorganic sulphide such as SO down
2, H
2S, sulfurous acid and sulfuric acid etc. and organic sulfide, electric field gets final product desorption when removing, and separable thus these class sulfur-bearing source of pollution are used for chemical industry, petroleum exhaust blowdown.Also available electric cracking disulfide linkage, sulfydryl organism promote protein degradations such as hair; Goods also have the anti-again galvanic corrosion of caoutchouc elasticity, oil resistant, directly are pasted on metal, inorganic or oil resistant spare open joint not, and are not only anticorrosion but also can seal, and prevent oil seepage.Both solve goods high-performance and moulding difficulty, awkward contradiction, greatly reduced raw material and energy expenditure again, avoided initial ring environment pollution in the production process simultaneously.
The objective of the invention is to realize by following measure:
A kind of is starting monomer with the aromatic series nitrogenous compound, with protonic acid or aprotic acid or aprotic acid salt serve as that row positions medium adopts a controlled architecture reaction methods of forming, the method for preparing high electric-activity conductive bending-resistant nanometre compound film is characterized in that also comprising as this law starting monomer:
(1) aliphatics disulphide and derivative thereof and performed polymer, their chemical structural formula:
H S-R-O-R-S H or H S-R-S H
Or H S-R-O-R-S
nH or H S-R-S
nH
R can be CH in the formula
2, C
2H
4Or C
3H
6N=5～40;
(2) and coloured glaze base thiazole and derivative and performed polymer, their chemical structural formula:
R in the formula
1Can be SH, CH
3, C
2H
5Or HS-R-SH; N=2～40;
(3) bis phenol-a epoxy resins of molecular weight 500～2O00;
Row position medium also comprises: acetonitrile, three fluoroacetic acid, trifluoroacetic acid, boron fluoric acid lithium LiBF
4, lithium perchlorate LiCLO
4, zinc perchlorate Zn (CLO
4)
2, magnesium perchlorate Mg (CLO
4)
2, aluminum perchlorate AL (CLO
4)
3, Witco 1298 Soft Acid and sodium salt thereof, aluminum chloride ALCL
3, cross Graphite Powder 99, the conductive carbon black of particle diameter 28～300nm, the aluminum phosphate ALPO of 200～400 mesh sieves
4, Tai-Ace S 150 AL
2(SO
4)
2, sodium perchlorate NaCLO
4, sodium sulfate Na
2SO
4, vinylformic acid, methyl acrylate, ethyl propenoate, butyl ester, methacrylic ester, polyacrylonitrile, paracril, and the concurrent mixture between them.
Monomeric concentration mole for well, is best with 0.125～1.0 with O.05～1.5;
The concentration of row positions medium mole for well, is best with 1～2 mole with O.5～4.
Selecting on row position medium and the monomeric basis, by adjusting condition control article constructions such as row position medium and monomer, performed polymer concentration and dispatch from foreign news agency, magnetic field, reaction times, envrionment temperature.
The present invention compared with prior art has following outstanding advantage:
1, utilizes two classes or/and the synergistic effect between the blend of the starting monomer more than two classes and multiple row position medium or multiple row position medium, the various performance index of goods are reached at energy environment protection, information sensing technology, biology---the suitable requirement in field such as medicine equipment, chemical separating are anticorrosion, automobile, electromagnetic interference shield and electrostatic dissipation, opened up the more wide purposes of high electric-activity conductive bending-resistant nanometre compound film.
2, the structure control of two kinds of polymkeric substance and other material in reaction and the combining of moulding, solved by powder blend such as polyaniline, organic disulfide itself crisp firmly, particle diameter greatly, extremely difficulty makes from the support film, the more difficult uniform mixing problem that reaches nanometer (molecule) level.
3, can directly make and be as thin as＜10～20 μ m composite membranes, area and shape can make by service requirements.This class composite membrane is during as electrode for secondary battery, oxidation---and reduction potential is poor＜0.05V, and in 50mV/ rose to the 100mV/S scope, this difference kept stablizing constant always, shows that to discharge and recharge reversible speed big, and it is little and stable to consume energy; When long-time (more than 60 minutes) electrochemical reduction or oxidation, can keep reducing or the current density of oxidation is stablized constantly, and can regulate the control current density value.
The oxidation of above-mentioned composite membrane---the reduction potential difference is than organic disulfide thing powder and the anodizing of polyaniline powder co-blended of Japanese Matsushita electrician company limited energy research chamber and Tokyo agrotechnique university cooperation---reduction potential is poor～little ten times of 0.5V.In addition, the polymkeric substance combined electrode after they improve, the oxidation current density value the during charging reduction current density value during still than discharge is high four times, can not regulate control.
4, the electric conductivity of making is up to the film more than the 100S/cm, at folding 180 ° after 50 times, both kept soft mechanical property, electric conductivity still kept～and 75%, than December nineteen ninety-five be that investigation of materials association is on the autumn session that Boston holds at MRS, the electrically conductive elastic plastics that the Neste company that Finland cooperates with the U.S. announces are when bending greater than 60 °, and electric conductivity has reduced by 100% and wanted much superior.
5, film of making or abnormal member, conduction has caoutchouc elasticity, oil-proofness again, and is good with polymkeric substance, metal, nonmetal stickup performance, both can be used for electrochemical anti-corrosive, can make the oil resistant sealing member again, has the good oil seepage ability that prevents.
6, the film of making itself is nontoxic, to organic sulfydryl or/and disulfide bond content can be little to 10
-5～10
-7Variation in the mol/L scope can reflect with linear relationship through micro voltage (in mV) or little electric current (mA) of this film, and easy-formation becomes the sensitive membrane of medical treatment transducer probe.
7, make the big area film under electric field action to inorganic sulphide such as SO
2, H
2S, sulfurous acid and sulfuric acid etc. have strong absorption and desorption with organic sulfide, this class sulfide can be separated from mixed gas, dust, liquid thus, as the crucial separatory membrane of waste-gas cleanings such as chemical industry, oil, boiler of power plant, mine, wastewater treatment blowdown.
8, make the film or the porous member of different shape, only impose the following electric field of 5V, just can greatly improve contain disulfide linkage or (with) degradation rate of sulfhydryl compound, as protein degradation promotion film (part) in the biotechnology etc.
The contriver once had many successful tests, now selected following 4 embodiment, thereby further specified content of the present invention.
Embodiment 1
By glass or plastics such as impact-resistant polystyrene is that material is made the rectangle electrolyzer.Adopt barrier film to be divided into the two chambers of equal-volume.In 1 liter acetonitrile solution, add the 2.0 moles of trichoroacetic acid(TCA)s of a medium of falling in lines, 1.0 moles of trifluoroacetic acids and 1.0 moles of aniline monomers and 0.125 mole of disulphide performed polymer H-S-CH
2CH
2-0-CH
2CH
2-S)
n-H, molecular weight are about 1000 (n=8～9), and selecting stainless steel substrates for use is working electrode, and high-purity carbon-point is that supporting electrode and mercurous chloride electrode are reference electrode.Control working electrode current potential is used current density 4mA/cm at 0.7～0.8V (VsSCE)
2Carry out the continuous current reaction.Temperature of reaction is normal temperature (23 ℃), reaction times is 10～20 minutes, make polyaniline/thiorubber composite membrane, thick＜10～20 μ m, oxidation when in 50mV/S to 100mV/S scope, changing cyclic voltammetry scan---reduction potential is poor～0.05V, the ratio of oxidation---reduction current peak value is near 1.
Embodiment 2
By glass or plastics impact-resistant polystyrene is that material is made electrolyzer.Without diaphragm for electrolytic cell.Add 1 liter propylene carbonate in the groove and make solvent, add 2.0 moles of trichoroacetic acid(TCA)s, 0.05 mole of paratoluenesulfonic acid sodium salt, 0.2 mole of pyrroles and 0.05 mole of disulphide performed polymer (molecular weight is about 1000) again.Selecting stainless steel substrates for use is working electrode and supporting electrode, and mercurous chloride electrode is a reference electrode, control constant current density 6mA/cm
2React, temperature of reaction is under 15 ℃, reaction times is 10～25 minutes, make translucent fexible film, thick 20 μ m, the smooth-flat-surface of being about, specific conductivity reaches 100S/cm, after 180 ° of doublings 50 times, electric conductivity still keeps about 75%, and (in the air) still keeps electroconductibility and mechanical property, softness under 100 ℃ of long-time heating.
Embodiment 3
By glass or plastics impact-resistant polystyrene is that material is made the rectangle electrolyzer.Adopt barrier film to be divided into the two chambers of equal-volume.In 1 liter acetonitrile solution, add 2.0 mole of three fluoroacetic acid, 0.8 mole of trifluoroacetic acid, 0.4 mole of aniline, 0.2 mole of disulphide performed polymer (molecular weight is 1500～2000).Selecting stainless steel substrates for use is that working electrode, high-purity carbon-point are that supporting electrode and mercurous chloride electrode are reference electrode.Control working electrode current potential is used current density 4.0mA/cm at 0.7～0.8V (VsSCE)
2React ,～23 ℃ of reactions 10～30 minutes, make the caoutchouc elasticity conductive composite film, thickness＜10～20 μ m, low temperature are chilled to-68 ℃ and still keep rubbery state (Tg=-68.5 ℃), are applicable to oil resistant low temperature resistant (below 60 ℃) sealing electric-conductor.
In the two-compartment cell of embodiment 4 with embodiment 3, in 1 liter acetonitrile solution, add 2.0 moles of trichoroacetic acid(TCA)s, 1.6 moles of aniline, 0.2 mole of disulphide performed polymer (molecular weight is about 500), 0.4 mole of bis phenol-a epoxy resins (molecular weight is about 1000).Selecting stainless steel substrates, carbon-point for use is work, supporting electrode and calomel reference electrode, uses current density 6.0mA/cm
2Reacted 5～10 minutes down at 23 ℃, getting viscosity increases but the viscous soln of good fluidity, from groove, take out, promptly get anti-galvanic corrosion coating such as carbon steel, cold rolling steel plate, in 110 ℃ of baking ovens, vacuumize to remove and desolvate, can get thick～0.04mm coating, have corrosion-resistant (the 5wt%NaCL aqueous solution) and ooze hole resistance rate and reach 2 * 10
9Ω, and anti-gasoline etc. (comprising aromatic hydrocarbons).
Maybe after reaction 5～10 minutes, the stainless steel substrates working electrode is taken out, change with carbon steel or cold rolling steel disc workmanship and make electrode, add current density 6.0mA/cm
2, 23 ℃ down reaction promptly apply the thick 0.03m of being about coating on the carbon steel coupon after 10 minutes, this coating aqueous solution of anti-5wt%NaCL ooze hole resistance rate＞2 * 10
9Ω, same anti-gasoline, aromatic hydrocarbons wet goods.
Claims (2)
1, a kind of is starting monomer with the aromatic series nitrogenous compound, salt with protonic acid or aprotic acid or aprotic acid serves as that row position medium adopts the controlled architecture reaction method of forming, the method for preparing high electric-activity conductive bending-resistant nanometre compound film is characterized in that also comprising as this law starting monomer:
(1) aliphatics disulphide and derivative thereof and performed polymer, their chemical structural formula:
HS-R-O-R-SH or HS-R-SH
Or H S-R-O-R-S
nH or H S-R-S
nH
R can be CH in the formula
2, C
2H
4Or C
3H
6N=5～40;
(2) thyroidan and derivative thereof and performed polymer, their chemical structural formula:
Or
Or
R1 can be SH, CH in the formula
3, C
2H
5Or HS-R-SH, n=2～40;
(3) molecular weight is 500～2000 bis phenol-a epoxy resins;
Row position medium also comprises: acetonitrile, trichoroacetic acid(TCA), trifluoroacetic acid, boron fluoric acid lithium LiBF
4, lithium perchlorate LiCLO
4, zinc perchlorate Zn (CLO
4)
2, magnesium perchlorate Mg (CLO
4)
2, aluminum perchlorate AL (CLO
4)
3, Witco 1298 Soft Acid and sodium salt thereof, aluminum chloride ALCL
3, cross Graphite Powder 99, the conductive carbon black of particle diameter 28～300mm, the aluminum phosphate ALPO of 200～400 mesh sieves
4, Tai-Ace S 150 AL
2(SO
4)
2, sodium perchlorate NaCLO
4, sodium sulfate Na
2SO
4, vinylformic acid, methyl acrylate, ethyl propenoate, butyl ester, methacrylic ester, polyacrylonitrile, paracril, and the concurrent mixture between them;
The concentration of starting monomer is 0.05～1.5 mole;
The concentration of row position medium is 0.5～4 mole.
2, the preparation method of high electric-activity conductive bending-resistant nanometre compound film according to claim 1, the optimum concn that it is characterized in that starting monomer is 0.125～1.0; The optimum concn of row position medium is 1～2 mole.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN96108338A CN1056164C (en) | 1996-06-25 | 1996-06-25 | Method for preparing high electric-activity conductive bending-resistant nanometre compound film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN96108338A CN1056164C (en) | 1996-06-25 | 1996-06-25 | Method for preparing high electric-activity conductive bending-resistant nanometre compound film |
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|---|---|
| CN1169443A true CN1169443A (en) | 1998-01-07 |
| CN1056164C CN1056164C (en) | 2000-09-06 |
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ID=5119937
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|---|---|---|---|
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1068885C (en) * | 1998-02-20 | 2001-07-25 | 华南理工大学 | Method for preparing polymer nanometre composite material |
| CN101440177B (en) * | 2008-12-11 | 2010-12-15 | 上海交通大学 | Preparation of polymer solid electrolyte |
| CN104925374A (en) * | 2015-05-21 | 2015-09-23 | 浙江海洋学院 | Purpose of nano-composite film for antibacterial isolation packaging |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5252835A (en) * | 1992-07-17 | 1993-10-12 | President And Trustees Of Harvard College | Machining oxide thin-films with an atomic force microscope: pattern and object formation on the nanometer scale |
| CN1041736C (en) * | 1992-08-04 | 1999-01-20 | 华南理工大学 | Method for preparing intrinsic conduction polymer microfibre, film and thick product |
| CN1040119C (en) * | 1994-08-29 | 1998-10-07 | 青岛化工学院 | Process for preparing nm-class conducting fibre |
-
1996
- 1996-06-25 CN CN96108338A patent/CN1056164C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1068885C (en) * | 1998-02-20 | 2001-07-25 | 华南理工大学 | Method for preparing polymer nanometre composite material |
| CN101440177B (en) * | 2008-12-11 | 2010-12-15 | 上海交通大学 | Preparation of polymer solid electrolyte |
| CN104925374A (en) * | 2015-05-21 | 2015-09-23 | 浙江海洋学院 | Purpose of nano-composite film for antibacterial isolation packaging |
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| Publication number | Publication date |
|---|---|
| CN1056164C (en) | 2000-09-06 |
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