CS273603B2 - Method of high-molecular electroconductive material production - Google Patents
Method of high-molecular electroconductive material production Download PDFInfo
- Publication number
- CS273603B2 CS273603B2 CS1065684A CS1065684A CS273603B2 CS 273603 B2 CS273603 B2 CS 273603B2 CS 1065684 A CS1065684 A CS 1065684A CS 1065684 A CS1065684 A CS 1065684A CS 273603 B2 CS273603 B2 CS 273603B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- formula
- group
- denotes
- weight
- polymer
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 8
- 238000000034 method Methods 0.000 title claims description 19
- 239000000463 material Substances 0.000 title abstract description 19
- 229920000642 polymer Polymers 0.000 claims abstract description 21
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims abstract description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 12
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 claims abstract description 11
- 230000007935 neutral effect Effects 0.000 claims abstract description 8
- IXHWGNYCZPISET-UHFFFAOYSA-N 2-[4-(dicyanomethylidene)-2,3,5,6-tetrafluorocyclohexa-2,5-dien-1-ylidene]propanedinitrile Chemical compound FC1=C(F)C(=C(C#N)C#N)C(F)=C(F)C1=C(C#N)C#N IXHWGNYCZPISET-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 7
- VRGCYEIGVVTZCC-UHFFFAOYSA-N 3,4,5,6-tetrachlorocyclohexa-3,5-diene-1,2-dione Chemical compound ClC1=C(Cl)C(=O)C(=O)C(Cl)=C1Cl VRGCYEIGVVTZCC-UHFFFAOYSA-N 0.000 claims abstract description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000004020 conductor Substances 0.000 claims abstract description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 6
- 239000011574 phosphorus Substances 0.000 claims abstract description 6
- 229910052785 arsenic Inorganic materials 0.000 claims abstract description 5
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000001424 substituent group Chemical group 0.000 claims abstract description 5
- 125000003118 aryl group Chemical group 0.000 claims abstract description 3
- 125000005842 heteroatom Chemical class 0.000 claims abstract description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims abstract 2
- 239000000654 additive Substances 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 13
- 230000000996 additive effect Effects 0.000 claims description 9
- 150000002605 large molecules Chemical class 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 6
- 238000001704 evaporation Methods 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 239000000370 acceptor Substances 0.000 abstract description 6
- 230000005670 electromagnetic radiation Effects 0.000 abstract description 2
- 239000005416 organic matter Substances 0.000 abstract description 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 239000005864 Sulphur Substances 0.000 abstract 1
- 238000012216 screening Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 description 13
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 230000007704 transition Effects 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
- 229920002239 polyacrylonitrile Polymers 0.000 description 4
- 239000004926 polymethyl methacrylate Substances 0.000 description 4
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000006259 organic additive Substances 0.000 description 2
- GMVPRGQOIOIIMI-DODZYUBVSA-N 7-[(1R,2R,3R)-3-hydroxy-2-[(3S)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]heptanoic acid Chemical compound CCCCC[C@H](O)C=C[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(O)=O GMVPRGQOIOIIMI-DODZYUBVSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K9/00—Screening of apparatus or components against electric or magnetic fields
- H05K9/0073—Shielding materials
- H05K9/0081—Electromagnetic shielding materials, e.g. EMI, RFI shielding
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G85/00—General processes for preparing compounds provided for in this subclass
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/121—Charge-transfer complexes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Chemical & Material Sciences (AREA)
- Electromagnetism (AREA)
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Electroluminescent Light Sources (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL24545083A PL139037B1 (en) | 1983-12-30 | 1983-12-30 | Method of obtaining high polymer material exibiting electric current conducting properties |
| PL25043684A PL142693B1 (en) | 1984-11-15 | 1984-11-15 | Method of obtaining a macromolecular material exibiting electrically conductive properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS1065684A2 CS1065684A2 (en) | 1990-08-14 |
| CS273603B2 true CS273603B2 (en) | 1991-03-12 |
Family
ID=26652996
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS1065684A CS273603B2 (en) | 1983-12-30 | 1984-12-29 | Method of high-molecular electroconductive material production |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0147871A3 (de) |
| CS (1) | CS273603B2 (de) |
| HU (1) | HUT37523A (de) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD301547A7 (de) * | 1987-04-09 | 1993-03-04 | Leipzig Tech Hochschule | Verfahren zur herstellung leitfaehiger strukturen in poly(organylheteroacetylenen) |
| EP0353760A3 (de) * | 1988-08-03 | 1991-01-16 | TDK Corporation | Flüssigkristallelemente und filmbildende leitende organische Zusammensetzung |
| US5231523A (en) * | 1988-08-03 | 1993-07-27 | Tdk Corporation | Liquid crystal elements and conductive organic compound film-forming compositions |
| FR2666438B1 (fr) * | 1990-08-30 | 1993-12-31 | Commissariat A Energie Atomique | Procede de fabrication en phase vapeur d'un ecran a base de polymere conducteur et ecran obtenu par ce procede. |
| FR2666439B1 (fr) * | 1990-08-30 | 1994-03-18 | Commissariat A Energie Atomique | Ecran absorbant a base de polymere conducteur electronique. |
| RU2256967C1 (ru) * | 2004-02-03 | 2005-07-20 | Кольцова Анастасия Андриановна | Электроактивный полимер и материал на его основе |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1241302A (en) * | 1967-08-03 | 1971-08-04 | Matsushita Electric Industrial Co Ltd | Heat-sensitive high molecular weight resistors |
| FR2102832A5 (en) * | 1970-08-25 | 1972-04-07 | California Inst Tech | Alkylated pyridine aldehyde in conductive c - ompositions |
| JPS4825041A (de) * | 1971-08-04 | 1973-04-02 | ||
| US4206308A (en) * | 1976-06-11 | 1980-06-03 | Matsushita Electric Industrial Co., Ltd. | Organic heat-sensitive semiconductive materials |
| DE3133738A1 (de) * | 1981-08-26 | 1983-03-10 | Bayer Ag, 5090 Leverkusen | Neue komplexsalze mit hoher elektrischer leitfaehigkeit |
-
1984
- 1984-12-29 HU HU489584A patent/HUT37523A/hu unknown
- 1984-12-29 CS CS1065684A patent/CS273603B2/cs unknown
- 1984-12-31 EP EP84116513A patent/EP0147871A3/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| EP0147871A3 (de) | 1986-01-08 |
| EP0147871A2 (de) | 1985-07-10 |
| HUT37523A (en) | 1985-12-28 |
| CS1065684A2 (en) | 1990-08-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4798685A (en) | Production of base-type conducting polymers | |
| Kanazawa et al. | ‘Organic metals’: polypyrrole, a stable synthetic ‘metallic’polymer | |
| Hotta et al. | Conducting polymer composites of soluble polythiophenes in polystyrene | |
| Diaz et al. | Synthesis, characterization and electrical properties of polyimines derived from selenophene | |
| US4935163A (en) | High service temperature conductive polymers and method of producing same | |
| Elsenbaumer et al. | Electrically conducting polyaromatic sulfides | |
| US20080241390A1 (en) | Insulating polymers containing polyaniline and carbon nanotubes | |
| FR2536079A1 (fr) | Polymeres electro-actifs et leur procede de production | |
| JPH06508874A (ja) | 開始剤による予備処理を採用しての導電性ポリマーフィルムの形成 | |
| Lee et al. | Synthesis and characterization of soluble polypyrrole | |
| Giesa | Synthesis and properties of conjugated poly (aryleneethynylene) s | |
| Goh et al. | Miscibility of polyaniline/poly (vinyl acetate) blends | |
| JP3400404B2 (ja) | 溶融加工または溶液加工可能な高度に導電性のポリアニリンおよびその製造方法並びにｐｖｃおよびｅｖａとこれとのブレンド | |
| Výprachtický et al. | New copolymers with thieno [3, 2‐b] thiophene or dithieno [3, 2‐b: 2′, 3′‐d] thiophene units possessing electron‐withdrawing 4‐cyanophenyl groups: Synthesis and photophysical, electrochemical, and electroluminescent properties | |
| Wan et al. | Transparent and conducting coatings of polyaniline composites | |
| Keller | Phthalonitrile‐based conductive polymer | |
| US4374048A (en) | Electrically conductive polymeric compositions | |
| EP0147871A2 (de) | Methode zur Herstellung hochmolekularen, elektrisch leitfähigen Materials | |
| US4886627A (en) | Conductive structures in polymers | |
| Bhandari et al. | Influence of reaction conditions on the formation of nanotubes/nanoparticles of polyaniline in the presence of 1‐amino‐2‐naphthol‐4‐sulfonic acid and applications as electrostatic charge dissipation material | |
| JP5993245B2 (ja) | 感湿素子及び湿度センサ | |
| US5776370A (en) | Charge transfer complexes between polyaniline and organic electron acceptors and method of fabrication | |
| US5407987A (en) | Polycyclic aromatic group - pendant polysilanes and conductive polymers derived therefrom | |
| Jeszka et al. | Surface-conductive polymer films by reticulate doping with organic metals | |
| SU1466650A3 (ru) | Способ получени полимерного пленочного материала |