JPS6065030A - 高分子フィルムの製造法 - Google Patents
高分子フィルムの製造法Info
- Publication number
- JPS6065030A JPS6065030A JP17340683A JP17340683A JPS6065030A JP S6065030 A JPS6065030 A JP S6065030A JP 17340683 A JP17340683 A JP 17340683A JP 17340683 A JP17340683 A JP 17340683A JP S6065030 A JPS6065030 A JP S6065030A
- Authority
- JP
- Japan
- Prior art keywords
- polymer film
- benzene
- film
- membered heterocyclic
- electrolytically
- 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.)
- Granted
Links
- 229920006254 polymer film Polymers 0.000 title claims abstract description 43
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000003115 supporting electrolyte Substances 0.000 claims abstract description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims abstract description 3
- 150000002391 heterocyclic compounds Chemical class 0.000 claims abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 2
- 238000001035 drying Methods 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims description 2
- XSOKHXFFCGXDJZ-UHFFFAOYSA-N telluride(2-) Chemical compound [Te-2] XSOKHXFFCGXDJZ-UHFFFAOYSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 abstract description 8
- 238000007254 oxidation reaction Methods 0.000 abstract description 8
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract description 4
- 239000002019 doping agent Substances 0.000 abstract description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 abstract 1
- 150000001555 benzenes Chemical class 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000012476 oxidizable substance Substances 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 150000003346 selenoethers Chemical class 0.000 abstract 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 6
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- KBLZDCFTQSIIOH-UHFFFAOYSA-M tetrabutylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC KBLZDCFTQSIIOH-UHFFFAOYSA-M 0.000 description 3
- 230000037303 wrinkles Effects 0.000 description 3
- QENGPZGAWFQWCZ-UHFFFAOYSA-N 3-Methylthiophene Chemical compound CC=1C=CSC=1 QENGPZGAWFQWCZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229920000128 polypyrrole Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- WGHUNMFFLAMBJD-UHFFFAOYSA-M tetraethylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CC[N+](CC)(CC)CC WGHUNMFFLAMBJD-UHFFFAOYSA-M 0.000 description 2
- RBWNDBNSJFCLBZ-UHFFFAOYSA-N 7-methyl-5,6,7,8-tetrahydro-3h-[1]benzothiolo[2,3-d]pyrimidine-4-thione Chemical compound N1=CNC(=S)C2=C1SC1=C2CCC(C)C1 RBWNDBNSJFCLBZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-O butylazanium Chemical compound CCCC[NH3+] HQABUPZFAYXKJW-UHFFFAOYSA-O 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 description 1
- 229920006391 phthalonitrile polymer Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- -1 tetra-n-butylammonium peroxide Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
Landscapes
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Formation Of Insulating Films (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17340683A JPS6065030A (ja) | 1983-09-19 | 1983-09-19 | 高分子フィルムの製造法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17340683A JPS6065030A (ja) | 1983-09-19 | 1983-09-19 | 高分子フィルムの製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6065030A true JPS6065030A (ja) | 1985-04-13 |
JPH0112775B2 JPH0112775B2 (enrdf_load_stackoverflow) | 1989-03-02 |
Family
ID=15959832
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17340683A Granted JPS6065030A (ja) | 1983-09-19 | 1983-09-19 | 高分子フィルムの製造法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6065030A (enrdf_load_stackoverflow) |
-
1983
- 1983-09-19 JP JP17340683A patent/JPS6065030A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0112775B2 (enrdf_load_stackoverflow) | 1989-03-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TW421808B (en) | Solid electrolytic capacitor and manufacture of the same | |
EP0342998A2 (en) | Process for manufacturing an electrode for a solid electrolytic capacitor | |
JP3074002B2 (ja) | 低級オリゴマーの酸化カップリングによる芳香族複素環式オリゴマーの製法 | |
JPS6065030A (ja) | 高分子フィルムの製造法 | |
EP0825618A2 (en) | Electrically-conductive polymer and production method thereof, and solid-electrolytic capacitor | |
JPS6411053B2 (enrdf_load_stackoverflow) | ||
JPH0112774B2 (enrdf_load_stackoverflow) | ||
JPH0274019A (ja) | 固体電解コンデンサの製造方法 | |
JPH0520449B2 (enrdf_load_stackoverflow) | ||
JP3242464B2 (ja) | 固体電解コンデンサの製造方法 | |
JPH0558227B2 (enrdf_load_stackoverflow) | ||
JPS62167330A (ja) | 有機高分子複合成形体の製造法 | |
JPH0727732B2 (ja) | 樹脂成形体表面の導電化方法 | |
JPH0419688B2 (enrdf_load_stackoverflow) | ||
JP3720603B2 (ja) | 導電性高分子材料および固体電解コンデンサ | |
JPS5943060A (ja) | 複素五員環式化合物重合体 | |
Miyamoto et al. | Electrochemistry of new heteroaromatic compounds of pyrrolopyrrole | |
JP2003192670A (ja) | 複素環芳香族化合物の金属錯体 | |
JPS6065031A (ja) | 高分子フィルムの製造法 | |
JPS6212063A (ja) | 二次電池 | |
JP2525488B2 (ja) | 高導電性ポリピロ―ル成形体 | |
JPH03220266A (ja) | 導電性高分子組成物 | |
JPH02103123A (ja) | 高強度全共役系ポリマーフィルムの製造方法 | |
JPH05136007A (ja) | 固体電解コンデンサおよびその製造方法 | |
JPH0611801B2 (ja) | 導電性フイルム |