KR100374719B1 - 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말제조방법 - Google Patents
가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말제조방법 Download PDFInfo
- Publication number
- KR100374719B1 KR100374719B1 KR10-2000-0065207A KR20000065207A KR100374719B1 KR 100374719 B1 KR100374719 B1 KR 100374719B1 KR 20000065207 A KR20000065207 A KR 20000065207A KR 100374719 B1 KR100374719 B1 KR 100374719B1
- Authority
- KR
- South Korea
- Prior art keywords
- acid
- ethylenedioxythiophene
- powder
- poly
- dopant
- 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.)
- Expired - Lifetime
Links
- 239000000843 powder Substances 0.000 title claims abstract description 41
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title claims abstract description 23
- -1 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 title claims description 15
- 238000002360 preparation method Methods 0.000 title description 4
- 239000002019 doping agent Substances 0.000 claims abstract description 20
- 239000003960 organic solvent Substances 0.000 claims abstract description 19
- 239000000178 monomer Substances 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 239000007800 oxidant agent Substances 0.000 claims abstract description 9
- 238000001035 drying Methods 0.000 claims abstract description 7
- 239000002904 solvent Substances 0.000 claims abstract description 7
- YMMGRPLNZPTZBS-UHFFFAOYSA-N 2,3-dihydrothieno[2,3-b][1,4]dioxine Chemical compound O1CCOC2=C1C=CS2 YMMGRPLNZPTZBS-UHFFFAOYSA-N 0.000 claims abstract description 4
- 230000000379 polymerizing effect Effects 0.000 claims abstract 2
- OGYMWUMPVDTUCW-UHFFFAOYSA-N 2,2-bis(2-ethylhexyl)-3-sulfobutanedioic acid Chemical group CCCCC(CC)CC(C(O)=O)(C(C(O)=O)S(O)(=O)=O)CC(CC)CCCC OGYMWUMPVDTUCW-UHFFFAOYSA-N 0.000 claims description 24
- GKWLILHTTGWKLQ-UHFFFAOYSA-N 2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=CSC=C21 GKWLILHTTGWKLQ-UHFFFAOYSA-N 0.000 claims description 22
- 159000000000 sodium salts Chemical class 0.000 claims description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 8
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 6
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 3
- 150000008050 dialkyl sulfates Chemical group 0.000 claims description 3
- 235000019253 formic acid Nutrition 0.000 claims description 3
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 claims description 2
- WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 claims description 2
- PTKWYSNDTXDBIZ-UHFFFAOYSA-N 9,10-dioxoanthracene-1,2-disulfonic acid Chemical compound C1=CC=C2C(=O)C3=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC=C3C(=O)C2=C1 PTKWYSNDTXDBIZ-UHFFFAOYSA-N 0.000 claims description 2
- JAJIPIAHCFBEPI-UHFFFAOYSA-N 9,10-dioxoanthracene-1-sulfonic acid Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2S(=O)(=O)O JAJIPIAHCFBEPI-UHFFFAOYSA-N 0.000 claims description 2
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 2
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 2
- IMBKASBLAKCLEM-UHFFFAOYSA-L ferrous ammonium sulfate (anhydrous) Chemical group [NH4+].[NH4+].[Fe+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O IMBKASBLAKCLEM-UHFFFAOYSA-L 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- LHOWRPZTCLUDOI-UHFFFAOYSA-K iron(3+);triperchlorate Chemical compound [Fe+3].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O LHOWRPZTCLUDOI-UHFFFAOYSA-K 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- FITZJYAVATZPMJ-UHFFFAOYSA-N naphthalene-2,6-disulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=CC2=CC(S(=O)(=O)O)=CC=C21 FITZJYAVATZPMJ-UHFFFAOYSA-N 0.000 claims description 2
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 claims description 2
- 239000012286 potassium permanganate Substances 0.000 claims description 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 claims 2
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005138 alkoxysulfonyl group Chemical group 0.000 claims 1
- 150000001343 alkyl silanes Chemical class 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 150000007942 carboxylates Chemical group 0.000 claims 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims 1
- VPCCKEJZODGJBT-UHFFFAOYSA-K iron(3+) phenylmethanesulfonate Chemical compound [Fe+3].[O-]S(=O)(=O)Cc1ccccc1.[O-]S(=O)(=O)Cc1ccccc1.[O-]S(=O)(=O)Cc1ccccc1 VPCCKEJZODGJBT-UHFFFAOYSA-K 0.000 claims 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 claims 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 claims 1
- 239000012046 mixed solvent Substances 0.000 claims 1
- 239000010452 phosphate Chemical group 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical group [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 1
- 230000035484 reaction time Effects 0.000 claims 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims 1
- PVEFEIWVJKUCLJ-UHFFFAOYSA-N sulfuric acid;toluene Chemical compound OS(O)(=O)=O.CC1=CC=CC=C1 PVEFEIWVJKUCLJ-UHFFFAOYSA-N 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 4
- 230000035699 permeability Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 20
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 18
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Divinylene sulfide Natural products C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 11
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 11
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 9
- 239000012153 distilled water Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000006096 absorbing agent Substances 0.000 description 6
- 239000010408 film Substances 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- 229930192474 thiophene Natural products 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 229920001940 conductive polymer Polymers 0.000 description 5
- 239000004983 Polymer Dispersed Liquid Crystal Substances 0.000 description 4
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000003990 capacitor Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000005669 field effect Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000005525 hole transport Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000001465 metallisation Methods 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000002121 nanofiber Substances 0.000 description 2
- 239000012454 non-polar solvent Substances 0.000 description 2
- 239000013307 optical fiber Substances 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 2
- 229960002796 polystyrene sulfonate Drugs 0.000 description 2
- 239000011970 polystyrene sulfonate Substances 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- RZCXRDBYLLLRKH-UHFFFAOYSA-N 2-(2-ethylhexyl)-2-sulfobutanedioic acid Chemical compound CCCCC(CC)CC(S(O)(=O)=O)(C(O)=O)CC(O)=O RZCXRDBYLLLRKH-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 238000001157 Fourier transform infrared spectrum Methods 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- HOCHJWBNDOKTEV-UHFFFAOYSA-K [Na+].C(C)C(CC(C(C(=O)[O-])S(=O)(=O)[O-])(C(=O)[O-])CC(CCCC)CC)CCCC.[Na+].[Na+] Chemical compound [Na+].C(C)C(CC(C(C(=O)[O-])S(=O)(=O)[O-])(C(=O)[O-])CC(CCCC)CC)CCCC.[Na+].[Na+] HOCHJWBNDOKTEV-UHFFFAOYSA-K 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229920001002 functional polymer Polymers 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- FLGQHZOFMJRAFO-UHFFFAOYSA-L iron(2+) toluene sulfate Chemical compound C1(=CC=CC=C1)C.S(=O)(=O)([O-])[O-].[Fe+2] FLGQHZOFMJRAFO-UHFFFAOYSA-L 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Abstract
Description
Claims (9)
- 하기에 기재된 일반식 (Ⅱ)인 도판트가 들어있는 용액에서 3,4-에틸렌다이옥시싸이오펜 단량체(일반식I)를 산화제를 사용하여 중합시킨 후 건조를 하여 이루어진 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말(일반식 Ⅲ)의 제조방법.
- 제 1항에 있어서,상기 도판트가 일반식 (Ⅱ)인 디(2-에틸헥실)설포숙신산 [또는 디(2-에틸헥실)설포숙신산의 나트륨염]인 것을 특징으로 하는 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
- 제 1항에 있어서,상기 도판트가 일반식 Ⅱ에서 R 및 R'가 탄소 2개∼20개의 알킬(alkyl), 이소오알킬(isoalkyl), 알콕시(alkoxy), 알콕시알킬(alkoxyalkyl), 알킬설퍼닐 (alkylsulfonyl), 알콕시설포닐 (alkoxysulfonyl), 알킬실란(alkylsilane), 알콕시실란(alkoxysilane), X가 설포네이트(sulfonate), 카르복실에이트(carboxylate), 포스페이트(phosphate), 설페이트(sulfate), 시아네이트(cyanate), 실리케이트(silicate) 등인 것을 특징으로 하는 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
- 제 1항에 있어서,상기 도판트가 탄소 2개∼20개의 디알킬설포숙신산(dialkylsulfosuccinic acid) [또는 디알킬설포숙신산의 염] 그리고 디알킬설포숙신산(dialkylsulfo succinic acid) [또는 디알킬설포숙신산의 염]과 방향족술폰산[aromatic sulfonic acid (benzenesulfonic acid, toluenesulfonic acid, sulfosalicylic acid, 2-naphthalene sulfonic acid, 2,6-naphthalenedisulfonic acid, naphthol-amino-disulfonic acid, anthraquinonesulfonic acid, anthraquinonedisulfonic acid, etc.)](혹은 방향족술폰산의 염)을 각각 혼합한 혼합도판트를 사용하는 것을 특징으로 하는 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
- 제 1항에 있어서,상기 도판트가 탄소 2개∼20개의 디알킬설포숙신산[또는 디알킬설포숙신산의 염]과 탄소 1개∼10개의 알킬(alkyl)기를 갖는 알킬설페이트 (또는 디알킬설페이트) 작용기를 각각 혼합한 혼합도판트를 사용하는 것을 특징으로 하는 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
- 제 1항에 있어서,상기 산화제는 황산암모늄철(ferrous ammonium sulfate), 황산철(ferric sulfate), 과염소산철(ferric perchlorate), 과망간산칼륨(potassium permanganate), 과산화칼륨(potassium persulfate), 2크롬산칼륨(potassium dichromate), 톨루엔황산철(Iron(Ⅲ)-toluene sulfonate)을 사용하는 것을 특징으로 하는 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
- 제 1항에 있어서,중합시 반응용액의 용매가 물, 유기용매[알콜류(부탄올, 메탄올, 에탄올, 프로판올, 이소오프로판올, 이소오부탄올 등) 클로로포름, 디클로로메탄, 아세트로나이트릴, 포름산, 아세트산 등)]이거나 물과 상기 유기용매와의 혼합용매에 의해 합성된 것을 특징으로 하는 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
- 제 1항에 있어서,중합시 -30℃ 이상 120℃ 이하의 반응온도하에서의 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
- 제 1항에 있어서,중합 반응 시간이 30분에서 72시간인 것을 특징으로 한 폴리(3,4-에틸렌다이옥시싸이오펜) 분말의 제조방법.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2000-0065207A KR100374719B1 (ko) | 2000-11-03 | 2000-11-03 | 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말제조방법 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2000-0065207A KR100374719B1 (ko) | 2000-11-03 | 2000-11-03 | 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말제조방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20020034723A KR20020034723A (ko) | 2002-05-09 |
KR100374719B1 true KR100374719B1 (ko) | 2003-03-04 |
Family
ID=19697134
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR10-2000-0065207A Expired - Lifetime KR100374719B1 (ko) | 2000-11-03 | 2000-11-03 | 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말제조방법 |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR100374719B1 (ko) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101000496B1 (ko) | 2008-09-19 | 2010-12-14 | (주)폴리메리츠 | 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 나노분말의 제조방법 |
KR101016260B1 (ko) | 2009-02-25 | 2011-02-25 | (주)수양켐텍 | 음이온 계면 활성제를 이용한 수분산 폴리(3, 4-에틸렌다이옥시싸이오펜)용액을 사용한 압전 필름스피커 |
KR101203596B1 (ko) | 2012-03-28 | 2012-11-21 | 주식회사진영케미칼 | Pet 시트용 대전방지 코팅조성물의 제조방법 |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100449820B1 (ko) * | 2002-07-02 | 2004-09-22 | 오재완 | 스크류형 연속식 금속분말 제조장치 |
KR100945056B1 (ko) * | 2008-05-20 | 2010-03-05 | (주)수양켐텍 | 유기 용제형 폴리(3, 4-에틸렌다이옥시싸이오펜) 용액의제조 방법 및 그 용액 |
KR100933441B1 (ko) * | 2008-09-09 | 2009-12-23 | (주)수양켐텍 | 음이온 계면 활성제를 이용한 수분산 폴리(3, 4-에틸렌다이옥시싸이오펜) 용액의 제조 방법 및 그 용액 |
EP2451850A4 (en) * | 2009-07-10 | 2013-08-07 | Univ Manitoba | IN-SITU POLYMERIZATION OF CONDUCTIVE POLY (3,4-ETHYLENE DIOXYTHIOPHONE) |
KR102791145B1 (ko) | 2019-06-14 | 2025-04-02 | 주식회사 엘지에너지솔루션 | 황-탄소 복합체, 이를 포함하는 리튬 이차전지용 양극 및 리튬 이차전지 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5035926A (en) * | 1988-04-22 | 1991-07-30 | Bayer Aktiengesellschaft | Method of imparting antistatic properties to a substrate by coating the substrate with a novel polythiophene |
US5300575A (en) * | 1990-02-08 | 1994-04-05 | Bayer Aktiengesellschaft | Polythiophene dispersions, their production and their use |
US5792558A (en) * | 1995-10-02 | 1998-08-11 | Bayer Aktiengesellschaft | Process for the electrostatic lacquering of non-conductive surfaces |
KR19990088611A (ko) * | 1998-05-29 | 1999-12-27 | 빌프리더 하이더 | 폴리(3,4-에틸렌디옥시티오펜)유도체를기재로하는자외선-안정전기변색조립체 |
KR19990088615A (ko) * | 1998-05-29 | 1999-12-27 | 빌프리더 하이더 | 전기발색층및이온저장층중의폴리(3,4-에틸렌디옥시티오펜)유도체기재의전기발색소자 |
KR20000001826A (ko) * | 1998-06-15 | 2000-01-15 | 유현식 | 고전도성 및 고투명성을 갖는 전도성 고분자의 제조방법 |
-
2000
- 2000-11-03 KR KR10-2000-0065207A patent/KR100374719B1/ko not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5035926A (en) * | 1988-04-22 | 1991-07-30 | Bayer Aktiengesellschaft | Method of imparting antistatic properties to a substrate by coating the substrate with a novel polythiophene |
US5300575A (en) * | 1990-02-08 | 1994-04-05 | Bayer Aktiengesellschaft | Polythiophene dispersions, their production and their use |
US5792558A (en) * | 1995-10-02 | 1998-08-11 | Bayer Aktiengesellschaft | Process for the electrostatic lacquering of non-conductive surfaces |
KR19990088611A (ko) * | 1998-05-29 | 1999-12-27 | 빌프리더 하이더 | 폴리(3,4-에틸렌디옥시티오펜)유도체를기재로하는자외선-안정전기변색조립체 |
KR19990088615A (ko) * | 1998-05-29 | 1999-12-27 | 빌프리더 하이더 | 전기발색층및이온저장층중의폴리(3,4-에틸렌디옥시티오펜)유도체기재의전기발색소자 |
KR20000001826A (ko) * | 1998-06-15 | 2000-01-15 | 유현식 | 고전도성 및 고투명성을 갖는 전도성 고분자의 제조방법 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101000496B1 (ko) | 2008-09-19 | 2010-12-14 | (주)폴리메리츠 | 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 나노분말의 제조방법 |
KR101016260B1 (ko) | 2009-02-25 | 2011-02-25 | (주)수양켐텍 | 음이온 계면 활성제를 이용한 수분산 폴리(3, 4-에틸렌다이옥시싸이오펜)용액을 사용한 압전 필름스피커 |
KR101203596B1 (ko) | 2012-03-28 | 2012-11-21 | 주식회사진영케미칼 | Pet 시트용 대전방지 코팅조성물의 제조방법 |
Also Published As
Publication number | Publication date |
---|---|
KR20020034723A (ko) | 2002-05-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6756473B2 (en) | Process for the preparation of neutral polyethylenedioxythiophene, and corresponding polyethylenedioxythiophenes | |
KR101082531B1 (ko) | 가용성 전도성 고분자 및 그의 제조 방법 | |
JP4974095B2 (ja) | 水溶性π共役重合体の製造方法 | |
KR20020040586A (ko) | 폴리티오펜 | |
KR20030010508A (ko) | 모노-, 올리고- 및 폴리-4-플루오로티오펜 및 전하 이동물질로서의 이들의 용도 | |
US8691117B2 (en) | Organic solvent dispersible conductive polymer and method for manufacture thereof | |
KR100374719B1 (ko) | 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 분말제조방법 | |
US8114316B2 (en) | Monomers, oligomers and polymers of thieno[2,3-b]thiophene | |
US8535571B2 (en) | Water-soluble electrically conductive polymers | |
KR20030069082A (ko) | 고전도율의 투명한 폴리티오펜 층 | |
KR100205912B1 (ko) | 가용 전기전도성 폴리아닐린의 제조방법 | |
WO2010041876A2 (ko) | 고분자 이온성 액체를 이용한 전도성 고분자 유기용매 분산용액 제조 방법 및 이에 의해 제조되는 전도성 고분자 | |
EP1284276B1 (en) | Conjugated copolymers of dithienothiophene with vinylene or acetylene | |
KR20010112574A (ko) | 여러 유기용매에 가용성인, 다양한 분자량의 폴리피롤제조방법 | |
KR100318153B1 (ko) | 알코올 및 다양한 유기용매에 대한 용해도가 높은 전도성 폴리피롤의 제조방법 | |
KR100437198B1 (ko) | 높은 용해성을 갖는 수용성 폴리피롤 및 그것의 제조방법 | |
KR101000496B1 (ko) | 가용성 폴리(3,4-에틸렌다이옥시싸이오펜) 나노분말의 제조방법 | |
KR100823635B1 (ko) | 이온 액체를 이용한 전도성 고분자의 나노입자의 제조방법및 이를 이용한 전도성 고분자 컴퍼지트 물질의 제조방법 | |
JP3164671B2 (ja) | アリーレンビニレン重合体およびその製造方法 | |
KR20020078926A (ko) | 가용성 폴리아닐린염 제조방법 | |
US5498477A (en) | N-phenylhydroxylamine polymers, and associated methods of preparation and use | |
KR20010109812A (ko) | 다양한 유기 극성용매에 용해성을 갖는 폴리아닐린 염의제조방법 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20001103 |
|
PA0201 | Request for examination | ||
PG1501 | Laying open of application | ||
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20021017 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20030127 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20030220 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20030221 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20060221 Start annual number: 4 End annual number: 4 |
|
PR1001 | Payment of annual fee |
Payment date: 20070220 Start annual number: 5 End annual number: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20080220 Start annual number: 6 End annual number: 6 |
|
PR1001 | Payment of annual fee |
Payment date: 20090220 Start annual number: 7 End annual number: 7 |
|
PR1001 | Payment of annual fee |
Payment date: 20100211 Start annual number: 8 End annual number: 8 |
|
PR1001 | Payment of annual fee |
Payment date: 20110216 Start annual number: 9 End annual number: 9 |
|
PR1001 | Payment of annual fee |
Payment date: 20120229 Start annual number: 10 End annual number: 10 |
|
FPAY | Annual fee payment |
Payment date: 20130218 Year of fee payment: 11 |
|
PR1001 | Payment of annual fee |
Payment date: 20130218 Start annual number: 11 End annual number: 11 |
|
FPAY | Annual fee payment |
Payment date: 20140217 Year of fee payment: 12 |
|
PR1001 | Payment of annual fee |
Payment date: 20140217 Start annual number: 12 End annual number: 12 |
|
FPAY | Annual fee payment |
Payment date: 20150817 Year of fee payment: 13 |
|
PR1001 | Payment of annual fee |
Payment date: 20150817 Start annual number: 13 End annual number: 13 |
|
FPAY | Annual fee payment |
Payment date: 20160819 Year of fee payment: 14 |
|
PR1001 | Payment of annual fee |
Payment date: 20160819 Start annual number: 14 End annual number: 14 |
|
PC1903 | Unpaid annual fee |
Termination category: Default of registration fee Termination date: 20171120 |
|
FPAY | Annual fee payment |
Payment date: 20171121 Year of fee payment: 15 |
|
PR0401 | Registration of restoration |
Patent event code: PR04011E01D Patent event date: 20171120 Comment text: Registration of Restoration |
|
PR1001 | Payment of annual fee |
Payment date: 20171121 Start annual number: 15 End annual number: 15 |
|
R401 | Registration of restoration | ||
PC1903 | Unpaid annual fee |
Termination category: Default of registration fee Termination date: 20181120 Termination category: Default of registration fee Termination date: 20171120 |
|
FPAY | Annual fee payment |
Payment date: 20181120 Year of fee payment: 16 |
|
PR0401 | Registration of restoration |
Patent event code: PR04011E01D Patent event date: 20181120 Comment text: Registration of Restoration |
|
PR1001 | Payment of annual fee |
Payment date: 20181120 Start annual number: 16 End annual number: 16 |
|
R401 | Registration of restoration | ||
FPAY | Annual fee payment |
Payment date: 20190218 Year of fee payment: 17 |
|
PR1001 | Payment of annual fee |
Payment date: 20190218 Start annual number: 17 End annual number: 17 |
|
FPAY | Annual fee payment |
Payment date: 20200220 Year of fee payment: 18 |
|
PR1001 | Payment of annual fee |
Payment date: 20200220 Start annual number: 18 End annual number: 18 |
|
PC1801 | Expiration of term |
Termination date: 20210503 Termination category: Expiration of duration Termination date: 20181120 Termination category: Default of registration fee Termination date: 20171120 Termination category: Default of registration fee |