TWI235387B - Electrically conductive composite particle and method for forming the same and application - Google Patents
Electrically conductive composite particle and method for forming the same and application Download PDFInfo
- Publication number
- TWI235387B TWI235387B TW92133594A TW92133594A TWI235387B TW I235387 B TWI235387 B TW I235387B TW 92133594 A TW92133594 A TW 92133594A TW 92133594 A TW92133594 A TW 92133594A TW I235387 B TWI235387 B TW I235387B
- Authority
- TW
- Taiwan
- Prior art keywords
- conductive composite
- item
- patent application
- composite particles
- conductive
- Prior art date
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- 239000011246 composite particle Substances 0.000 title claims abstract description 120
- 238000000034 method Methods 0.000 title claims abstract description 83
- 229920001940 conductive polymer Polymers 0.000 claims abstract description 54
- 239000002563 ionic surfactant Substances 0.000 claims abstract description 27
- 229920000867 polyelectrolyte Polymers 0.000 claims abstract description 24
- 239000003381 stabilizer Substances 0.000 claims abstract description 12
- 238000006116 polymerization reaction Methods 0.000 claims description 46
- -1 α-alkylstyrene Chemical compound 0.000 claims description 40
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 36
- 239000000243 solution Substances 0.000 claims description 32
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 24
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 23
- 230000008569 process Effects 0.000 claims description 23
- 125000002091 cationic group Chemical group 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 20
- 229920000642 polymer Polymers 0.000 claims description 20
- 239000007864 aqueous solution Substances 0.000 claims description 19
- 239000004094 surface-active agent Substances 0.000 claims description 17
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 16
- 239000002904 solvent Substances 0.000 claims description 16
- 239000000178 monomer Substances 0.000 claims description 15
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 14
- 239000010949 copper Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 13
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 12
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 239000010408 film Substances 0.000 claims description 11
- 230000002209 hydrophobic effect Effects 0.000 claims description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 10
- 239000005977 Ethylene Substances 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 10
- 239000006185 dispersion Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- ODPYDILFQYARBK-UHFFFAOYSA-N 7-thiabicyclo[4.1.0]hepta-1,3,5-triene Chemical compound C1=CC=C2SC2=C1 ODPYDILFQYARBK-UHFFFAOYSA-N 0.000 claims description 8
- 229910019142 PO4 Inorganic materials 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 8
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 8
- 239000010452 phosphate Substances 0.000 claims description 8
- 230000000087 stabilizing effect Effects 0.000 claims description 8
- 229930192474 thiophene Natural products 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 239000003093 cationic surfactant Substances 0.000 claims description 7
- 239000010409 thin film Substances 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 6
- 229910052742 iron Inorganic materials 0.000 claims description 6
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 6
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 5
- 239000013543 active substance Substances 0.000 claims description 5
- 229920001448 anionic polyelectrolyte Polymers 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 150000002500 ions Chemical class 0.000 claims description 5
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 5
- 229920000768 polyamine Polymers 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 claims description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
- 229910004064 NOBF4 Inorganic materials 0.000 claims description 4
- 229910004074 SiF6 Inorganic materials 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- AEJIMXVJZFYIHN-UHFFFAOYSA-N copper;dihydrate Chemical compound O.O.[Cu] AEJIMXVJZFYIHN-UHFFFAOYSA-N 0.000 claims description 4
- 238000004512 die casting Methods 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
- QZRHHEURPZONJU-UHFFFAOYSA-N iron(2+) dinitrate nonahydrate Chemical compound O.O.O.O.O.O.O.O.O.[Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O QZRHHEURPZONJU-UHFFFAOYSA-N 0.000 claims description 4
- IZEMHEXSGIOXDA-UHFFFAOYSA-N iron;hexahydrate Chemical compound O.O.O.O.O.O.[Fe] IZEMHEXSGIOXDA-UHFFFAOYSA-N 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 230000006641 stabilisation Effects 0.000 claims description 4
- 238000011105 stabilization Methods 0.000 claims description 4
- 229910021592 Copper(II) chloride Inorganic materials 0.000 claims description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 229910021576 Iron(III) bromide Inorganic materials 0.000 claims description 3
- 229910021578 Iron(III) chloride Inorganic materials 0.000 claims description 3
- 229910002567 K2S2O8 Inorganic materials 0.000 claims description 3
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims description 3
- 229910004069 NO2BF4 Inorganic materials 0.000 claims description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
- 229920002873 Polyethylenimine Polymers 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 3
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 229910000365 copper sulfate Inorganic materials 0.000 claims description 3
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 3
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 3
- 229910000366 copper(II) sulfate Inorganic materials 0.000 claims description 3
- 150000002430 hydrocarbons Chemical group 0.000 claims description 3
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 3
- 239000000155 melt Substances 0.000 claims description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 3
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 claims description 3
- 235000019394 potassium persulphate Nutrition 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 230000003068 static effect Effects 0.000 claims description 3
- FEONEKOZSGPOFN-UHFFFAOYSA-K tribromoiron Chemical compound Br[Fe](Br)Br FEONEKOZSGPOFN-UHFFFAOYSA-K 0.000 claims description 3
- 239000000052 vinegar Substances 0.000 claims description 3
- 235000021419 vinegar Nutrition 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 2
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- 150000001409 amidines Chemical class 0.000 claims description 2
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 claims description 2
- YHGPYBQVSJBGHH-UHFFFAOYSA-H iron(3+);trisulfate;pentahydrate Chemical compound O.O.O.O.O.[Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O YHGPYBQVSJBGHH-UHFFFAOYSA-H 0.000 claims description 2
- 229910000462 iron(III) oxide hydroxide Inorganic materials 0.000 claims description 2
- 239000000693 micelle Substances 0.000 claims description 2
- 150000004690 nonahydrates Chemical class 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims 3
- 239000002131 composite material Substances 0.000 claims 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 2
- 229910052802 copper Inorganic materials 0.000 claims 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 claims 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 claims 1
- 235000017491 Bambusa tulda Nutrition 0.000 claims 1
- 241001330002 Bambuseae Species 0.000 claims 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims 1
- 102000003992 Peroxidases Human genes 0.000 claims 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 claims 1
- 241000270708 Testudinidae Species 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 235000019270 ammonium chloride Nutrition 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims 1
- 239000011425 bamboo Substances 0.000 claims 1
- YRNNKGFMTBWUGL-UHFFFAOYSA-L copper(ii) perchlorate Chemical compound [Cu+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O YRNNKGFMTBWUGL-UHFFFAOYSA-L 0.000 claims 1
- 230000005611 electricity Effects 0.000 claims 1
- 238000002309 gasification Methods 0.000 claims 1
- 125000003010 ionic group Chemical group 0.000 claims 1
- HQPMOXUTKURVDV-UHFFFAOYSA-L iron(2+);sulfate;pentahydrate Chemical compound O.O.O.O.O.[Fe+2].[O-]S([O-])(=O)=O HQPMOXUTKURVDV-UHFFFAOYSA-L 0.000 claims 1
- 108040007629 peroxidase activity proteins Proteins 0.000 claims 1
- 150000003014 phosphoric acid esters Chemical class 0.000 claims 1
- 229920002401 polyacrylamide Polymers 0.000 claims 1
- 229920005862 polyol Polymers 0.000 claims 1
- 150000003077 polyols Chemical class 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- SRRKNRDXURUMPP-UHFFFAOYSA-N sodium disulfide Chemical compound [Na+].[Na+].[S-][S-] SRRKNRDXURUMPP-UHFFFAOYSA-N 0.000 claims 1
- 239000003990 capacitor Substances 0.000 abstract description 4
- 239000002216 antistatic agent Substances 0.000 abstract 1
- 239000003973 paint Substances 0.000 abstract 1
- 239000004984 smart glass Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 description 9
- 239000004816 latex Substances 0.000 description 8
- 229920000126 latex Polymers 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 239000011258 core-shell material Substances 0.000 description 4
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000002609 medium Substances 0.000 description 3
- BNJMRELGMDUDDB-UHFFFAOYSA-N $l^{1}-sulfanylbenzene Chemical compound [S]C1=CC=CC=C1 BNJMRELGMDUDDB-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 239000007771 core particle Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229960001922 sodium perborate Drugs 0.000 description 2
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 1
- AKOVMBAFZSPEQU-UHFFFAOYSA-N 2-methylhex-2-enoic acid Chemical compound CCCC=C(C)C(O)=O AKOVMBAFZSPEQU-UHFFFAOYSA-N 0.000 description 1
- FHIDNBAQOFJWCA-UAKXSSHOSA-N 5-fluorouridine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(F)=C1 FHIDNBAQOFJWCA-UAKXSSHOSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- MDVUQSWBRKRIBG-UHFFFAOYSA-N [S]CC1=CC=CC=C1 Chemical compound [S]CC1=CC=CC=C1 MDVUQSWBRKRIBG-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- SQHOHKQMTHROSF-UHFFFAOYSA-N but-1-en-2-ylbenzene Chemical compound CCC(=C)C1=CC=CC=C1 SQHOHKQMTHROSF-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- WXYNCCWBUXKSBG-UHFFFAOYSA-N copper;nitric acid Chemical compound [Cu].O[N+]([O-])=O WXYNCCWBUXKSBG-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- RYPKRALMXUUNKS-UHFFFAOYSA-N hex-2-ene Chemical compound CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- XBDUTCVQJHJTQZ-UHFFFAOYSA-L iron(2+) sulfate monohydrate Chemical compound O.[Fe+2].[O-]S([O-])(=O)=O XBDUTCVQJHJTQZ-UHFFFAOYSA-L 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- GYCHYNMREWYSKH-UHFFFAOYSA-L iron(ii) bromide Chemical compound [Fe+2].[Br-].[Br-] GYCHYNMREWYSKH-UHFFFAOYSA-L 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000004686 pentahydrates Chemical class 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002098 polyfluorene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
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- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
Description
1235387 玖、發明說明: 【發明所屬之技術領域】 本發明係有關於—插道 種導電性複合粒子及其形成方法 與應用,特別是有關於一 、 種具有離子型穩定劑之導電性 複合粒子及其形成方法與應用。 【先前技術】 共軛性導電高分子具有介於半導體與金屬導體間的 導電特性’其潛在的應用範圍相當廣泛,如:發光二極 體 '導電電極、防腐蝕塗梦、辨 思土衣、k色®戶、電容器等。故 近年來,許多學者赭_ 、 扠入龐大心力進行開發與研究。 '、而*於:^員刀子具有共軛性的主鏈結構,造成其在 -般有機溶劑中的溶解度甚低且㈣融溫度,也使得它 的加工及模“生均極為困難,因此大幅限制了共概性導 電高分子的實際應用範圍。為瞭解決上述之加工問題, 一個有效的方法是將導電高分子製備為穩定性膠體,尤 其以水作為連續相分散液爭 刀月又成更月匕進一步降低有機溶劑的 使用,減少環境污染。 由於導電性高分子係為一硬脆性材料,目而,其成 膜性與機械強度通常不佳。最為常用的改良方法乃將此 等共軛性分子摻以一般性聚合體。歐洲專利申請案 EP0589529 #示了一種導電性核殼乳膠及其製備方 法,該方法係在高分子乳膠粒子表面上吸附一層非離子 13 1235387 型穩定劑,然後,外殼再吸附一層導電性高分子,以穩 定此高分子膠體,避免發生凝集(coagulation)而產生沈 β 殿。其中所使用的非離子型穩定劑包括p〇lyOXyalkyi esters 和 polyoxyalkyl ethers,分子量係介於 500 至 5 0 00g/m〇l。惟此外殼導電性高分子之厚度需介於非離 子型穩定劑在介質中所伸展的長度内,若此導電性核殼 乳膠外殼之含量比例太大,則導電性高分子之厚度超過 非離子型穩定劑層,將造成乳膠粒子不安定而凝結。相 鲁 對地,若此導電性核殼乳膠外殼之含量比例太小,則導 電層太薄,將可能無法獲得所期望之導電度,其中所揭 不之導電乳膠係使用於電磁波遮蔽體、抗靜電塗料等用 途0 另外,法國專利申請案FR 2616790則描述一種高 分子核心粒子被一個導電性高分子外殼所環繞,此高分1235387 发明 Description of the invention: [Technical field to which the invention belongs] The present invention relates to—insulating conductive composite particles and methods and applications for forming the same, and particularly to one or more conductive composite particles having an ionic stabilizer. And its formation method and application. [Previous technology] Conjugated conductive polymers have conductive properties between semiconductors and metal conductors, and their potential applications are quite wide, such as: light-emitting diodes, conductive electrodes, anti-corrosion Tumen, speculative earth coat, k color ® households, capacitors, etc. Therefore, in recent years, many scholars have devoted great efforts to development and research. ', And * Yu: ^ member knife has a conjugated main chain structure, which causes its solubility in ordinary organic solvents to be very low and the melting temperature, which also makes its processing and mold production extremely difficult, so Limits the practical application range of co-conductive conductive polymers. In order to solve the above processing problems, an effective method is to prepare conductive polymers as stable colloids, especially using water as a continuous phase dispersion. Moon Dagger further reduces the use of organic solvents and reduces environmental pollution. Since the conductive polymer is a hard and brittle material, its film-forming properties and mechanical strength are usually poor. The most commonly used improvement method is to conjugate these The sex molecule is mixed with a general polymer. European patent application EP0589529 # shows a conductive core-shell latex and a preparation method thereof. The method is to adsorb a layer of a nonionic 13 1235387 type stabilizer on the surface of a polymer latex particle, and then, The outer shell absorbs another layer of conductive polymer to stabilize the polymer colloid and prevent coagulation from occurring, which can lead to the formation of Shen β. Sub-type stabilizers include pOlyOXyalkyi esters and polyoxyalkyl ethers, with molecular weights ranging from 500 to 5000 g / mol. However, the thickness of the conductive polymer in the shell needs to be between that of the non-ionic stabilizer stretched in the medium. In the length, if the content ratio of this conductive core-shell latex shell is too large, the thickness of the conductive polymer exceeds the non-ionic stabilizer layer, which will cause the latex particles to be unstable and coagulate. Relatively, if this conductivity The content ratio of the core-shell latex shell is too small, and the conductive layer is too thin, and the desired conductivity may not be obtained. The uncovered conductive latex is used for electromagnetic wave shields, antistatic coatings, etc. 0 In addition, French patents Application FR 2616790 describes a polymer core particle surrounded by a conductive polymer shell.
子核〜係包括 alkyd resin、acrylate resin 及 polyurethane等,其中所揭示之導電核殼粒子分散液, 係用於導電塗佈,惟此高分子核心粒子表面需有doping group存在,且乳膠粒子極易受反應條件之影響而產生 凝集沈澱等情形’例如在殼層單體氧化聚合的過程中或 離子性化合物 如氧化劑之加入均易造成系統之不穩定。 有鑑於此,仍有必要發展新的導電性複合粒子的 造方法以形成更穩定的導電性複合粒子並提供更簡易 14 1235387 製程’以符合產業上的需求。 【發明内容】 寥於上述之發明背景中,為了提供更簡易的製程盘 形成更穩定的導電性複合粒子’本發明提供—種新:導 電性複合粒子及其形成方法與應用,以符合產業上的= 求。 本發明之一目的在於製造出一穩定的導電性複合粒 子’本發明可在水相系統中使用至少一種水溶性之離子 型穩定劑穩定具有至少—種非導電性高分子之第—往 構’亦可在水相介質中進行-聚合反應以形成一具有: 少一種導電性高分子之笫—έ士搂 lL ^ 第一結構,此製程步驟相當簡 易,且可在水相系統中執行, 田曰 仃所以無洛劑易揮發以及 成污染等缺點。 ° 本發明之另一目的在於形成基本導電材料,例如以 溶液鋒造法或熔融㈣法製成導電薄膜或直接塗佈於非 導電基材上以製造導雷其# . 导電基材,本技術可應用於具導電 性、金屬化、防電磁波幹擾、 一 设及具抗静電性質等材料盘 兀件之製造,例如:發光二極體、 ^ 壯‘ $篮導電電極、防腐蝕塗 裝、變色窗戶、電容器箄 因此,本發明能符合經濟上 的效益與產業上的利用性。 根據以上所述之目的,本 人 本發明揭不了 一種導電性複 合粒子及其形成方法與應用, 此V冤性複合粒子包含一 15 1235387 具有至少-種非導電性高分子之第_結構、—具有至少 -種導電性高分子之第二結構與至少一種離子型穩定 劑’此離子型穩定劑更包含一離子型介面活性劑與一聚 電解質。另外’本發明也揭示了導電性複合粒子之形成 方法及其應用。 【實施方式】 本發明在此所探討的方向為—種導電性複合粒子及 ,、形成方法與應用。為了能徹底地瞭解本發明,將在下 列的描述中提出詳盡的製程步驟或組 本發明的施行並未限定於導電性複合粒子領域=者 =Γ殊…另,,眾所一:::: 步驟並未描述於细銥 、 从4衣矛王 砍於、、·田即中,以避免造成本 制。本發明的較佳音^ 月不必要之限 孝又佳貫轭例會詳細描述如 些詳細描述之外’本發明還可以 除了這 施例中,且本發明的r圍不^ “也仃在其他的實 圍為準。 乾圍不$限定’其以之後的專利範 在本發明之—第_實施例中,主 複合粒子,此g 要棱供一種導電性 b導電性複合粒子包含:, 導電性高分子之第-結構呈有至/、有至少-種非 子之第二結構,此第二結構_由二—種導電性高分 一結構表面上, 9 聚合反應形成於第 /、至少一種離子 八 型介面活性劑4 ά f "面活性劑,此離子 糟由靜m力鍵結㈣L穩定 16 1235387 該導電性複合粒子之結構,其中 面與至少一種離子_ a 孓第—結構的表 種離子型介面活性劑之 面,導電性複合粒子可料於一溶媒中二另-方 液,其中,上述之溶媒更包含-水相溶液。::一:散 液可藉由-成膜製程以形成—導電薄;;人:散 程更包含-溶液塗佈法。另外,導電性複 =製程以形成一導電薄膜,此處之成膜製程更!含 一:=法。上述之導電性複合粒子的製造方法包含 ?合程序以混合第-結構與至少一種離子型介面活性 翁一溶媒中並使得離子型介面活性_由靜電吸引力 鍵結第-結構之表面’藉此穩定第一結構及形成一穩定 夜-中’上述之穩定液的傑塔電位之絕對值範圍約大 於l〇mV,其較佳範圍約大於2〇mV,其最佳範圍約大 於 3OmV。 在本實施例中,上述之第一結構係藉由至少一種聚 口單元所聚合而成,其中,上述之至少一種聚合單元包 含下列族群中之一者:烷基丙烯酸酯、烷基甲基丙烯酸 酷、乙烯單體(例如苯乙烯、α -烷基苯乙烯、乙酸乙稀 酯、氣乙烯、二氣乙烯、丙烯腈、甲基丙烯腈、二乙烯 本)與含經基的不飽和化合物(如卢-經乙基丙烯酸酉旨、点 乙基曱基丙烤酸醋、里丙基丙稀酸g旨、經丙基甲美丙 烯酸醋),又上述之至少一種聚合單元更包含一募聚物。 17 1235387 另一方面,上述之第二結構係藉由至少一種聚合單元所 聚合而成,其中,上述之至少—種聚合單元包含下列族 群中之一者:苯胺(―)、^各(pyrr〇1〇、售吩 Uhi〇phene)、咬喃(furan)、乙炔(acetyiene)、笨 基硫(Phenylene sulfide )及其衍生物又上述之至少 一種聚合單元更包含一募聚物。 在本實施例中,當上述之離子型介面活性劑係為降 料型介面活性劑時,其疏水端係為匕至C2。院基、燒 芳基與烯基所組成之族群中的一者,且陰離子型介面: 性劑的親水端係為硫酸根、續酸根、魏根、聚氧化乙 烯硫酸根、聚氧化乙烯磷酸根與具有陰離子型基團之_ :所組:之族群中的-者,其中,上述之鹽類係為心 疏鉍鹽與二級胺基鹽所組成之族群中的一者;告上 述之離子型介面活性劑係為陽離子型介面活性劑,2 水端係為c4至p I w e 、一 C20烷基、烷方基與烯基所組成之族群中 的-者’且陽離子型介面活性劑的親 基團與陽離子型基^鹽類所組成之族群中的 外’上述之離子型介面活性劑更包含一兩性 2 另方面,若所製造的導電性複合粒子包含 聚本乙烯之第一結構、一且 /、有 -種離子型介丨弟·"結構與至少 著離子型介面= 述之第二結構的厚度會隨 面活性劑之疏水端的鏈長增加而增加。 18 1235387 在 子,此 導電性 子之第 第一結 子型介 結構, 構之外 子型介 面活性 本貫施例中,更接 托仏—種較佳之導電性複合粒 較佳之導電性複合 粒子包含:一具有至少一種非 高分子之第一纟士楼 、、。構、一具有至少一種導電性高分 -、-構’此第二結構係藉由一聚合反應形成於該 構表面上 帛-離子型介面活性劑,此第一離 面活U之親水端係藉由靜電吸引力鍵結該第一 措此,第一離子The daughter core ~ includes alkyd resin, acrylate resin, polyurethane, etc. The conductive core-shell particle dispersion disclosed therein is used for conductive coating, but the doping group exists on the surface of the polymer core particle, and the latex particles are extremely easy Agglomeration and sedimentation under the influence of reaction conditions, such as during the oxidative polymerization of shell monomers or the addition of ionic compounds such as oxidants, can easily cause system instability. In view of this, it is still necessary to develop new manufacturing methods of conductive composite particles to form more stable conductive composite particles and provide a simpler 14 1235387 process' to meet the needs of the industry. [Summary of the Invention] In the above background of the invention, in order to provide a simpler process disc to form more stable conductive composite particles, the present invention provides a new type: conductive composite particles and methods and applications for forming the same, in order to meet the industrial requirements = = Find. One object of the present invention is to produce a stable conductive composite particle. The present invention can use at least one water-soluble ionic stabilizer in an aqueous phase system to stabilize the first structure of at least one non-conductive polymer. It can also be polymerized in an aqueous medium to form a polymer with one of the following: one of the least conductive polymers—the first structure. This process is relatively simple and can be performed in an aqueous system. Therefore, there are no shortcomings such as volatile agents and pollution. ° Another object of the present invention is to form a basic conductive material, for example, a conductive thin film made by a solution front method or a molten aluminum method or directly coated on a non-conductive substrate to manufacture a conductive substrate #. The technology can be applied to the manufacture of disc components with materials such as conductivity, metallization, anti-electromagnetic interference, and antistatic properties, such as: light-emitting diodes, conductive electrodes, anti-corrosion coating , Color-changing windows, and capacitors. Therefore, the present invention can meet economic benefits and industrial applicability. According to the above-mentioned purpose, the present invention does not disclose a conductive composite particle, a method for forming the composite particle, and an application thereof. The V composite particle includes a 15 1235387 structure having at least one non-conductive polymer, having The second structure of at least one conductive polymer and at least one ionic stabilizer. The ionic stabilizer further includes an ionic surfactant and a polyelectrolyte. In addition, the present invention also discloses a method for forming conductive composite particles and its application. [Embodiment] The direction explored by the present invention is a kind of conductive composite particles, and its formation method and application. In order to fully understand the present invention, detailed process steps or groups will be proposed in the following description. The implementation of the present invention is not limited to the field of conductive composite particles. The steps are not described in fine iridium, chopped from the 4th King of Spears, and · Tian Jizhong to avoid causing this system. The preferred embodiment of the present invention is described in detail in addition to the unnecessary filial piety and good consistency. 'The present invention can also be used in this embodiment, and the r of the present invention is not "^" The actual circumference shall prevail. The dry circumference is not limited. The following patents are in the present invention-the first embodiment, the main composite particle, which is to provide a conductive b conductive composite particle including :, conductive The first structure of the polymer has a second structure with up to / and at least one species. This second structure is formed from two or more highly conductive structures on the surface. Ionic eight-type surface active agent 4 ά f " Surface active agent, this ion is stabilized by static bond ㈣L 16 1235387 The structure of the conductive composite particle, wherein the surface and at least one ion _ a 孓 第 —structure table As for the surface of an ionic surfactant, the conductive composite particles can be expected in one solvent and two liquid solutions. Among them, the above-mentioned solvent further includes an aqueous solution. :: One: The liquid dispersion can be processed by a film-forming process. In order to form-conductive thin; people: the dispersion range is more inclusive-soluble Liquid coating method. In addition, the conductive complex process is used to form a conductive thin film, and the film-forming process here is even more! Contains one: = method. The above-mentioned manufacturing method of the conductive composite particles includes a combination process to mix the first structure And at least one ionic interface active in a solvent and make the ionic interface active _ the surface of the first structure is bonded by electrostatic attractive force, thereby stabilizing the first structure and forming a stable night-medium The absolute range of the tower potential is greater than about 10 mV, its preferred range is greater than about 20 mV, and its optimal range is greater than about 30 mV. In this embodiment, the first structure described above is implemented by at least one type of aggregation unit. Polymerized, wherein at least one of the above-mentioned polymerization units includes one of the following groups: alkyl acrylates, alkyl methacrylates, ethylene monomers (eg, styrene, α-alkylstyrene, ethyl acetate Esters, ethylene gas, digas ethylene, acrylonitrile, methacrylonitrile, divinyl) and unsaturated compounds containing a radical (such as Lu-Ethyl Acrylic Acid) Propylpropene g purpose, via propylmethacrylic acid vinegar), and at least one of the above-mentioned polymerized units further comprises a polymer. 17 1235387 On the other hand, the above-mentioned second structure is polymerized by at least one polymerized unit, wherein At least one of the above-mentioned polymerization units includes one of the following groups: aniline (-), pyrrO10, UhiOphene, furan, acetyiene, benzyl sulfur (Phenylene sulfide) and its derivatives and at least one of the above-mentioned polymerization units further include an agglomerate. In this embodiment, when the above-mentioned ionic surfactant is a reduced-type surfactant, its hydrophobic end is It is from C2 to C2. One of the group consisting of courtyard, burned aryl and alkenyl, and anionic interface: The hydrophilic end of the agent is sulfate, continuous acid, Wei root, polyethylene oxide sulfate, Polyoxyethylene phosphate and _ with an anionic group:-Group:-Among the above, the above-mentioned salts are one of the group consisting of cardiophosphine and secondary amine salts ; Report the above ionic interface activity It is a cationic surfactant, and the 2 water end is the one of the group consisting of c4 to p I we, a C20 alkyl group, an alkyl group, and an alkenyl group, and the parent group of the cationic surfactant and The above-mentioned ionic surfactants in the group consisting of cationic groups and salts further include an amphoteric 2 On the other hand, if the conductive composite particles produced include the first structure of polyethylene, one and /, There is a kind of ionic interface. The structure and at least the ionic interface = the thickness of the second structure will increase as the chain length of the hydrophobic end of the surfactant increases. 18 1235387 In this embodiment, the first junction-type mesostructure of this conductive proton, and the activity of the exon-type meso-type interface are further supported in this embodiment—a better conductive composite particle. A better conductive composite particle includes: A first parlor with at least one non-polymer. A second structure is formed by a polymerization reaction on the surface of the structure with an at least one highly conductive-,-structure. The hydrophilic end of the first off-surface active U is The first measure is bonded by electrostatic attraction, the first ion
t "面活性劑之疏水端向第一結 側L伸肖帛二離子型介面活性劑,此第二離 面活性劑之疏水端ϋ由親…結第—離子型介 背j之“水编,且第二離子型介面活性劑之親水端 向第-結構之外側延伸以穩定導電性複合粒子之結構, 八中上述之第離子型介面活性劑可等同於第二離子 型介面活性劑。The hydrophobic end of t " surfactant is extended to the first junction side of the diionic surfactant, and the hydrophobic end of the second off-surface surfactant is formed by the "water" of the ionic interface. And the hydrophilic end of the second ionic surfactant is extended to the outside of the first structure to stabilize the structure of the conductive composite particles. The above-mentioned first ionic surfactant may be equivalent to the second ionic surfactant.
在本發明之一第二實施例中,主要提供一種導電性 複合粒子,該導電性複合粒子包含:一具有至少一種非 導電H问刀子之第一結構;一具有至少一種導電性高分 第…構’此第二結構係藉由一聚合反應形成於第 一結構表面上,與至少一種聚電解質,此聚電解質係藉 由靜電吸引力鍵結第-結構以穩定導電性複合粒子。另 方面導電性複合粒子可懸浮於一溶媒中以形成一分 =液,其中,上述之溶媒更包含一水相溶液。其次,分 散液可藉由一成膜製程以形成一導電薄膜,此處之成膜 19 !235387 製程更包含—溶液塗佈法。另外,導電性複合粒子可藉 由-成膜製程以形成一導電薄膜,此處之成膜製程更包 含一熔融壓鑄法。 在本實施例中’上述之第一結構係藉由至少一種聚 合單元所聚合而成’其中’上述之至少一種聚合 包含下列族群中之一者··院基丙埽酸醋、烧基甲基丙烯 酸酉旨、乙烯單體(例如苯乙烤、α_院基苯乙稀、乙酸乙 婦自旨、氯乙烯、二氣乙稀、丙烯腈、甲基丙烯腈、二乙 烯笨)與含烴基的不飽和化合物(如f經乙基丙烯酸 H經乙基甲基丙稀酸酷、經丙基丙烯酸醋、經丙基 甲基丙烯酸酯)’又上述之至少一種聚合單元更包含一募 :物。另-方面’上述之第二結構係藉由至少一種聚合 單元所聚合而成’其中’上述之至少一種聚合單元包含 下列族群中之—者:苯胺(aniline)、料(pyrrole)、 噻吩(thiophene )、呋喃(furan )、乙炔(acetyiene )、 苯基硫(phenylene sulfide)及其衍生物。,又上述之 至少一種聚合單元更包含一寡聚物。 在本實施例中,當上述之聚電解質係為陰離子型聚 電解質,則其係為具有醯胺、磺酸根、磷酸根與有機磷 酸酯之高分子所組成之族群中的一者;當上述之聚電解 質係為陽離子型聚電解質,則其係為聚醯胺 (polyamine)、含有胺基(amines)之陽離子型改質聚丙 20 1235387 酿、含有季胺基(qUaternized amines)之陽離子型改質 t丙醢、I乙稀亞胺(p〇lyethyleneimine)與聚二丙烯 基二甲基氣化銨【poly ( diallyl dimethyl amm〇nium chloride)】所組成之族群中的一者。 在本發明之一第三實施例中,首先提供一具有至少 -種非導電性高分子之材f,然後,進行—混合程序以 混合該具有至少一種非導電性高分子之材質與至少一種 離子型介面活性劑於-溶媒中,此溶媒更包含—水相溶 液。上述之混合程序的目的為藉由離子型介面活性劑的 静電吸引力鍵結具有至少一種非導電性高分子之材質的 表面,並ϋ此穩定該具有至少—種非導電性高分子之材 質及形成-穩定液,其中,上述之具有至少一種非導電 性高分子之材質的表面係與至少一種離子型介面活性劑 之電性相反。而且,上述之穩定液所含的至少一種離子 型介面活性劑濃度範圍約為至少一 门夕種離子型介面活性劑 之臨界微胞濃度(critical micelle咖咖⑽―)之 L至五倍。其-人’上述之穩定液的傑塔電位之絕對值 範圍約大於1 OmV,其較祛銘圄从 八权佳乾圍約大於20mV,其最佳 範圍約大& 3〇mV。於混合程序完成後,添加至少一種 導電高分子聚合單元與至少一綠 種化學助劑於穩定液中以 使得至少一種導電高分子聚合單 口平7L進仃一聚合反應並形 成導電性複合粒子。 21 1235387 在本實施例中,當卜、+·—私7 離子型介面活性劑,,…ΓΓ子型介面活性劑係為陰 关糞, 、/、馼水端係為C4至c20烷基、垸 方基與烯基所組成之 八二 群中的一者。又上述之陰離子型 :;活性劑的親水端係為硫酸根、續酸根、碟酸根、聚 ^乙烯硫酸根、聚氧化乙烯磷酸根與具有陰離子型基 之鹽類所組成之族群中的一者, 八干上述之鹽類係 驗金屬帛、銨鹽與三級胺基鹽所組成之族群令的— 者’田上述之離子型介面活性劑係為陽離子型介面活性 劑’則其疏水端係為匕至〜院基、烧芳基與稀基所組 成之族群中的—者。又上述之陽離子型介面活性劑的親 水端係為陽離子型基團與陽離子型基團之鹽類所組成之 埃群中的一者°此外’上述之離子型介面活性劑更包含 〜兩性介面活性劑。 在本實施例中,上述之至少一種導電高分子聚合單 元包含下列族群之一者:苯胺(aniline )、吡咯 (pyrrole )、噻吩(thiophene )、呋喃(如扣)、乙炔 (acetylene )、苯基硫(phenylene sulfide )及其衍生 物,其中,上述之至少一種導電高分子聚合單元更包含 〜券聚物。另外,上述之至少一種化學助劑係為下列族 鮮之一者··過硫酸鉀(K2S2〇8 )、過硫酸銨【(NH4 ) 以2〇8】、過硫酸鈉(Na2S2〇8 )、其他過硫酸鹽、過硼酸 鈉(NaB〇3)、過氧化氫(h2〇2)、N〇BF4、N〇2BF4、 22 1235387 NO2PF6、NOC1〇4、NOAsF6、NO2PF6、溴 4匕鐵(FeBr3 )、 六水合氣化鐵(FeCIs · 6H2O )、硫酸銅(CuSCU )、九 水合硝酸鐵【Fe(N〇3)3· 9H2〇】,二水合氣化銅(CuCl2 · 2H2O )、鐵氰化鉀【K3Fe(CN}6】、硝酸銅【Cu(N03)2】、 Fe(BF4)3、九水合過氣酸鐵【Fe(Cl〇4)3· 9H2〇】、五水In a second embodiment of the present invention, a conductive composite particle is mainly provided. The conductive composite particle includes: a first structure having at least one non-conductive H-knife; one having at least one conductive high score ... The second structure is formed on the surface of the first structure by a polymerization reaction with at least one polyelectrolyte. The polyelectrolyte is bonded to the first structure by electrostatic attraction to stabilize the conductive composite particles. On the other hand, the conductive composite particles can be suspended in a solvent to form a liquid. The above-mentioned solvent further includes an aqueous solution. Secondly, the dispersion liquid can be formed into a conductive thin film by a film forming process, and the film forming process here includes a solution coating method. In addition, the conductive composite particles can be formed into a conductive thin film by a film-forming process, and the film-forming process here further includes a melt die-casting method. In the present embodiment, the above-mentioned first structure is formed by polymerization of at least one polymerization unit, wherein the at least one polymerization described above includes one of the following groups: Acrylic acid purpose, ethylene monomers (such as styrene ethyl roast, alpha-ethyl styrene, ethyl acetate, vinyl chloride, digas, acrylonitrile, methacrylonitrile, divinyl) and hydrocarbon groups Unsaturated compounds (such as f via ethyl acrylate, H via ethyl methyl acrylate, via propyl acrylate, via propyl methacrylate), and at least one of the above-mentioned polymerization units further includes a compound: . In another aspect, the above-mentioned second structure is formed by polymerizing at least one polymerization unit, wherein the at least one polymerization unit includes one of the following groups: aniline, pyrrole, and thiophene. ), Furan, acetyiene, phenylene sulfide, and derivatives thereof. Furthermore, at least one of the above-mentioned polymerization units further comprises an oligomer. In this embodiment, when the above-mentioned polyelectrolyte is an anionic polyelectrolyte, it is one of the group consisting of polymers including amidine, sulfonate, phosphate, and organic phosphate; when the above-mentioned The polyelectrolyte is a cationic polyelectrolyte, which is a polyamine, a cationic modified polypropylene containing amines 20 1235387, and a cationic modified containing qUaternized amines. One of the groups consisting of propane, polyethylenimine and poly (diallyl dimethyl ammonium chloride). In a third embodiment of the present invention, a material f having at least one non-conductive polymer is first provided, and then, a mixing process is performed to mix the material having at least one non-conductive polymer with at least one ion. The surface-active agent is in a solvent, and the solvent further includes an aqueous solution. The purpose of the above mixing procedure is to bond the surface of a material having at least one non-conductive polymer by the electrostatic attractive force of the ionic surface active agent, and thereby stabilize the material having at least one non-conductive polymer. And a forming-stabilizing solution, wherein the surface of the above-mentioned material having at least one non-conductive polymer is opposite to that of at least one ionic surfactant. Moreover, the concentration range of the at least one ionic surfactant in the above-mentioned stabilizing solution is about L to five times the critical micelle concentration of at least one ionic surfactant. The absolute value of the Jetta potential of the above-mentioned stabilizing solution is greater than about 1 OmV, which is about 20 mV larger than that of Ququanjiaquan, and the optimal range is about 30 mV. After the mixing process is completed, at least one conductive polymer polymerization unit and at least one green chemical assistant are added to the stabilization solution so that at least one conductive polymer polymerization unit 7L flatly undergoes a polymerization reaction and forms conductive composite particles. 21 1235387 In this embodiment, when D. + · —— 7 ionic surface active agent, ... ΓΓ sub-type surface active agent is Yin Guan feces, and /, water end system is C4 to c20 alkyl, One of the eighty-two groups consisting of stilbene and alkenyl. The above anionic type: the hydrophilic end of the active agent is one of the group consisting of sulfate, dibasic acid, discic acid, polyvinyl sulfate, polyethylene oxide phosphate, and salts having anionic groups. The eight dry salts mentioned above are tested in a group consisting of metal rhenium, ammonium salts and tertiary amine salts. If the above-mentioned ionic surfactant is a cationic surfactant, its hydrophobic end is For those who belong to the courtyard group, burned aryl group and dilute base group. The hydrophilic end of the above-mentioned cationic surfactant is one of the EG group composed of a cationic group and a salt of the cationic group. In addition, the above-mentioned ionic surfactant further includes an amphoteric interface activity. Agent. In this embodiment, the at least one conductive polymer polymerization unit includes one of the following groups: aniline, pyrrole, thiophene, furan (such as buckle), acetylene, phenyl Sulfur (phenylene sulfide) and its derivatives, in which at least one of the above-mentioned conductive polymer polymerization units further comprises a ~ polymer. In addition, at least one of the above-mentioned chemical additives is one of the following groups: potassium persulfate (K2S208), ammonium persulfate [(NH4) 208], sodium persulfate (Na2S208), Other persulfates, sodium perborate (NaB〇3), hydrogen peroxide (h2O2), NOBF4, NO2BF4, 22 1235387 NO2PF6, NOC104, NOAsF6, NO2PF6, bromine 4 iron (FeBr3) , Iron hexahydrate gas (FeCIs · 6H2O), copper sulfate (CuSCU), iron nitrate nonahydrate [Fe (N〇3) 3. 9H2〇], copper hydrate gas (CuCl2 · 2H2O), potassium ferricyanide [K3Fe (CN} 6], copper nitrate [Cu (N03) 2], Fe (BF4) 3, ferric acid nonahydrate [Fe (Cl〇4) 3 · 9H2〇], pentahydrate
合硫酸鐵【Fe2(S04)3 · 5H2〇】、Fe2(SiF6)3、過氯酸鋼 【Cu(C104)2】、Cu(bf4)2、CuSiF6。上述之至少一種化 學助劑的用量與至少一種導電高分子聚合單元用量之莫 耳比範圍約為1 : 1 〇至1 〇 ·· 1,其中最佳之比例範圍約 為為1 : 3至3 : 1,且過量之至少一種化學助劑可於聚 合反應後以離心等程序除去。 在本發明之一第四實施例中,首先提供一具有至 一種非導電性高分子之材質,然《,進行-混合程序 此a 4具有至少一種非導電性高分子之材質與至少一Ferric sulfate [Fe2 (S04) 3 · 5H2〇], Fe2 (SiF6) 3, Perchloric acid steel [Cu (C104) 2], Cu (bf4) 2, CuSiF6. The molar ratio of the amount of the at least one chemical additive mentioned above to the amount of at least one conductive polymer polymerization unit ranges from about 1:10 to 10.0 · 1, and the optimal ratio ranges from about 1: 3 to 3 : 1, and the excess of at least one chemical assistant can be removed by a procedure such as centrifugation after the polymerization reaction. In a fourth embodiment of the present invention, a material having at least one non-conductive polymer is first provided.
聚電解質於-溶媒+,此溶媒更包含-水相溶液。上 之此口轾序的目的為藉由聚電解質的靜電吸引力鍵結 有至少-種非導電性高分子之材質的表面,並藉此穩 具有至少-種非導電性高分子之材f及形成—穩定液 其人添加至少一種導電高分子聚合單元與至少一種 學助劑於穩定液中 e ^ 使侍至少一種導電高分子聚合單 進行$ 口反應並形成導電性複合粒子。 在本貫施例中,备 田上述之聚電解質係為陰離子型 23 1235387The polyelectrolyte is in -solvent +, and the solvent further comprises -aqueous solution. The purpose of this sequence is to bond the surface of a material with at least one non-conductive polymer by the electrostatic attractive force of the polyelectrolyte, and thereby stabilize the material with at least one non-conductive polymer f and Formation-stabilizing solution. The person adds at least one conductive polymer polymerization unit and at least one chemical aid to the stabilization liquid. The reaction solution is formed by at least one conductive polymer polymerization unit and forms conductive composite particles. In this example, the above-mentioned polyelectrolyte of Biata is anionic 23 1235387
電解質’則其係為具有醯胺、磺酸根、磷酸根與有機碟 酸醋之高分子所組成之族群中的一者;當上述之聚電解 質也為陽離子型聚電解質,則其係為聚醯胺 (polyamine)、含有胺基(amines)之陽離子型改質聚 丙醯、含有季胺基(qUat;ernized amines)之陽離子型改 質聚丙醯、聚乙稀亞胺(p〇lyethyieneimine)與聚二丙 稀基 '一甲基氣化錢【poly ( diallyl dimethyl ammonium chloride )】所組成之族群中的一者。其 次,上述之至少一種導電高分子聚合單元包含下列族群 之一者:苯胺(aniline)、°比洛(pyrrole)、售吩 (thiophene )、呋喃(fur an )、乙炔(ace tylene )、 苯基硫(phenylene sulfide)及其衍生物。上述之至 少一種導電高分子聚合單元更包含一寡聚物。此外,上 述之至少一種化學助劑係為下列族群之一者:過硫酸鉀 (K2S2O8 )、過硫酸銨【(NHU ) 2S2〇8】、過硫酸鈉 (Na2S2〇8)、其他過硫酸鹽、過硼酸鈉(NaB〇3)、過 氧化氫(H2O2)、NOBF4、NO2BF4、N〇2PF6、N0C1〇4、 NOAsF6、N〇2PF6、溴化鐵(FeBr3 )、六水合氣化鐵 (FeCl3 · 6H2O )、硫酸銅(CuS〇4 )、九水合硝酸鐵 【Fe(N03)3 · 9H2〇】,二水合氣化銅(CuCl2 · 2H2〇 )、 鐵氰化鉀【K3Fe(CN)6】、硝酸銅【Cu(N03)2】、 Fe(BF4)3、九水合過氣酸鐵【Fe(Cl〇4)3· 9H2O】、五 24 I235387 水合硫酸鐵【Fe2(S〇4)3 · 5H2〇】、Fe2(SiF6)3、過氣酸 麵1【Cu(Cl〇4)2】、Cu(BF4)2、CuSiF6。上述之至少一 種化學助劑的用量與至少一種導電高分子聚合單元用 夏之莫耳比範圍約為1 : 1 0至1 0 : 1,其中最佳之比例 範園約為為1 : 3至3 : 1,且過量之至少一種化學助劑 可於聚合反應後以離心等程序除去。 在本發明之一第五實施例中,首先提供含有3 w1: 0/〇 體含量的聚苯乙烯乳膠水溶液1 〇ml。接著,以去離子 水稀釋至20ml並加入鹽酸水溶液酸化上述之稀釋液至 PH值約為〇·7以形成一起始液。然後,添加含有 〇· 1150克的十二烧基績酸鈉(s〇diuin dodecyl sulfonate ,SDS )陰離子型界面活性劑水溶液2〇ml 至上述之起始液中並進行一混合程序。該混合程序係於 一第一溫度範圍内進行,此第一溫度範圍約為〇它至 10 °c,其較佳溫度範圍為i t至5 t,上述之混^ 程序約進行12小時以形成一穩定液。於混合程序完i 後,加入1.53/z 1苯胺單體溶液於上述之穩定液中並於 拌約-小日寺。最後,加入含有〇· 〇〇43克的過硫酸銨^ 溶液1〇 mi以進行一聚合反應。上述之聚合反應更包^ -第-步驟與-第二步驟,帛一步驟係於第一溫度範匿 内執行,而第二步驟係於一第二溫度範圍内執行,其中 第二溫度範圍之溫度約高於第一溫度範圍。而1,第一 25 1235387 步驟進行約6個小時,而第-牛 乐—步驟進行約1 8個小時。 完成上述程序後,可製造出-導電性複合粒子,此導電 性複合粒子包含:一具有聚苯乙烯之第一結構一具有 聚苯胺之第二結構’此第二結構係藉由一聚合反應形成 於第一結構表面上,與十-e ”丁 一坑基磺酸鈉(sodium dodecyl sulfonate,SDS),jl 筏益丄 y 而 ;具係稭由靜電吸引力鍵結 第一結構以穩定導電性複合粒子之結構。 在本發明之一第六實施例中 貝匕1夕』T,改變苯胺單體溶液為 與含有〇._6克的過硫酸銨水溶液i〇mu 他如同第五實施例的操作條件,所得之導電性複合粒子 粉末經磨細後壓片,測得之導電度為2 〇9xi〇 ss/cm。 在本發明之-第七實施例中,改變陰離子型界面活 性劑為含t 0.055克的十四…酸鈉(減⑽ tetradec^ sulfonate)之水溶〉夜2〇mi、苯胺單體溶液 為15.3/^與含有0.0430克的過硫酸敍水溶液ι〇 m卜其他如同第五實施例的操作條件,所得之導電性複 合粒子粉末經磨細後壓片,測得之導電度為Ο.〗% S / cm。 在本發明之—第人實施例中,改變苯胺單體溶液為 與含有0.0215克的過硫酸銨水溶液i〇mi,其 他如同第五實施例的操作條件,所得之導電性複合粒子 粉末經磨細後壓片,測得之導電度為〇 i26 s/cm。 26 l235387 在本發明之一第九實施例中,改變苯胺單體溶液為 9·18//1與含有00258克的過硫酸錄水溶液i〇mi,其 他如同第五實施例的操作條件,所得之導電性複合粒子 粉末經磨細後壓片,測得之導電度為〇· 157 s/cm。 在本發明之一第十實施例中,改變苯胺單體溶液為 與含有0.043克的過硫酸銨水溶液1〇 ml,其 他如同第五實施例的操作條件,所得之導電性複合粒子 粉末經磨細後壓片,測得之導電度為〇162 s/cm。 在本發明之一第十一實施例中,改變苯胺單體溶液 為24.8//1與含有0.0688克的過硫酸銨水溶液1〇 如1,其他如同第五實施例的操作條件,所得之導電性複 合粒子粉末經磨細後壓片,測得之導電度為Q145 S / cm 〇 在本發明之一第十二實施例中,改變苯胺單體溶液 為30.6//1與含有0.086克的過硫酸銨水溶液1(3瓜卜 其他如同第五實施例的操作條件,所得之導電性複合粒 子粉末經磨細後壓片,測得之導電度為〇115 s/cm。 在本發明之一第十二實施例中,改變陰離子型界面 活性劑為含有0.055克的十四烷基磺酸納(s〇dium tetradecyi sUlfonate)之水溶液2〇mi、苯胺單體溶液 為9·18/^與含有0·0258克的過硫酸銨水溶液ι〇 m卜其他如同第五實施例的操作條件,所得之導電性複 27 !235387 口粒子粉末經磨細後壓片,測得之導電度為〇 1 〇6 S/cm。 在本發明之一第十四實施例中,改變苯胺單體溶液* 為6.12“;!與含有〇.〇172克的過硫酸銨水溶液】〇 ' ml,其他如同第五實施例的操作條件,所得之導電性複 合粒子粉末經磨細後壓片,測得之導電度為2.69x1()-2 S/cm。 在上述本發明之實施例中,本發明揭示了—種穩定肇 的導電ί±複合粒子及其形成方法,本發明可在水相系統 中使用至少一種水溶性之離子型穩定劑穩定具有至少一 種非導電性高分子之第一結構,亦可在水相介質中進行 聚合反應以形成一具有至少一種導電性高分子之第二 σ構此製程步驟相當簡易,且可在水相系統中執行, 所以無溶劑易揮發以及造成污染等缺點。另外,本發明 更揭路以溶液鑄造法或熔融壓鑄法製成導電薄膜或直接 _ 塗佈於非導電基材上以製造導電基材,由此可見,本技 =可應用於具導電性、金屬化、防電磁波干擾、及具抗 靜電性質等材料與元件之製造,例如:發光二極體、導 電電極、防腐蝕塗裝、變色窗戶、電容器等。因此,本 發明能符合經濟上的效益與產業上的利用性。 綜合以上所述,本發明揭示了 一種導電性複合粒子 及其形成方法與應用,此導電性複合粒子包含一具有至 28 Ϊ235387 --種非導電性高分子之第一結構、— 電抖古八, 種導 W刀子之第二結構與至少一種離子型 子刑指a μ 此離 I疋劑更包含一離子型介面活性劑與一聚電解質。 另外,本發明也揭示了導電性複合粒子之形成方法及: 應用。 其 顯然地,依照上面實施例中的描述,本發明 。+夕的修正與差異。因此需要在其附加的權利要求項之 範圍内加以理解,除了上述詳細的描述外,本發明還可 以廣泛地在其他的實施例中施行。上述僅為本發明之, 佳實施例而已’並非用以限定本發明之申請專利範圍: 凡其它未脫離本發明所揭示 ’ 不之精神下所完成的等效改變 或修飾’均應包含在下述申請專利範圍内。"Electrolyte" is one of the group consisting of polymers containing ammonium amine, sulfonate, phosphate, and organic vinegar; when the above polyelectrolyte is also a cationic polyelectrolyte, it is a polyfluorene Polyamines, cationic modified polypropylene containing amines, modified cationic containing polyamines (qUat; ernized amines), polyethyieneimine and polydiamine One of the groups consisting of poly (diallyl dimethyl ammonium chloride). Second, the at least one conductive polymer polymerization unit includes one of the following groups: aniline, pyrrole, thiophene, fur an, ace tylene, phenyl Sulfur (phenylene sulfide) and its derivatives. At least one of the above-mentioned conductive polymer polymerization units further includes an oligomer. In addition, at least one of the aforementioned chemical additives is one of the following groups: potassium persulfate (K2S2O8), ammonium persulfate [(NHU) 2S2〇8], sodium persulfate (Na2S208), other persulfates, Sodium perborate (NaB〇3), hydrogen peroxide (H2O2), NOBF4, NO2BF4, No2PF6, NOC104, NOAsF6, No2PF6, iron bromide (FeBr3), iron hexahydrate gaseous iron (FeCl3 · 6H2O ), Copper sulfate (CuS〇4), iron nitrate nonahydrate [Fe (N03) 3 · 9H2〇], gasified copper dihydrate (CuCl2 · 2H2〇), potassium ferricyanide [K3Fe (CN) 6], nitric acid Copper [Cu (N03) 2], Fe (BF4) 3, iron peroxahydrate [Fe (Cl〇4) 3 · 9H2O], five 24 I235387 iron sulfate hydrate [Fe2 (S〇4) 3 · 5H2〇 ], Fe2 (SiF6) 3, peroxy acid surface 1 [Cu (Cl〇4) 2], Cu (BF4) 2, CuSiF6. The amount of the at least one chemical additive mentioned above and the summer mole ratio of the at least one conductive polymer polymerization unit range from about 1:10 to 10: 1, and the optimal ratio is about 1: 3 to 3: 1, and the excess of at least one chemical assistant can be removed by a procedure such as centrifugation after the polymerization reaction. In a fifth embodiment of the present invention, first, 10 ml of a polystyrene latex aqueous solution containing a 3 w 1: 0 / 〇 volume content is provided. Next, it was diluted to 20 ml with deionized water and the above diluted solution was acidified by adding an aqueous hydrochloric acid solution to a pH of about 0.7 to form a starting solution. Then, 20 ml of an aqueous solution of anionic surfactant containing 0.115 g of sodium dodecyl sulfonate (SDS) was added to the above-mentioned starting solution and a mixing procedure was performed. The mixing process is performed in a first temperature range, the first temperature range is about 0 to 10 ° c, and the preferred temperature range is it to 5 t. The above mixing process is performed for about 12 hours to form a Stabilizing fluid. After the mixing procedure is complete, add the 1.53 / z 1 aniline monomer solution to the above-mentioned stabilization solution and mix in the small-day temple. Finally, a solution containing 0.043 g of ammonium persulfate ^ was added to 10 mi to perform a polymerization reaction. The above-mentioned polymerization reaction is more inclusive.-The first step and the second step, the first step is performed within a first temperature range, and the second step is performed within a second temperature range. The temperature is approximately higher than the first temperature range. While 1, the first 25 1235387 step takes about 6 hours, and the first-Niu Le-step takes about 18 hours. After completing the above procedures, conductive composite particles can be manufactured. The conductive composite particles include: a first structure having polystyrene and a second structure having polyaniline. This second structure is formed by a polymerization reaction. On the surface of the first structure, it is combined with sodium dodecyl sulfonate (SDS), jl raft and y; and the first structure is bonded to the first structure by electrostatic attraction to stabilize the conductivity. The structure of the composite particles. In one sixth embodiment of the present invention, the aniline monomer solution was changed to an aqueous solution containing 0.1 g of ammonium persulfate aqueous solution. Under the conditions, the obtained conductive composite particle powder was ground and pressed into a tablet, and the measured conductivity was 209 x 60 ss / cm. In the seventh embodiment of the present invention, the anionic surfactant was changed to contain t 0.055g of water soluble sodium tetradec ^ sulfonate> 20min at night, aniline monomer solution of 15.3 / ^ and 0.0430g of persulfuric acid aqueous solution ιOMm other than the fifth embodiment Operating conditions, resulting conductivity The composite particle powder was ground and pressed into tablets, and the measured conductivity was 0%% S / cm. In the first embodiment of the present invention, the aniline monomer solution was changed to a solution containing 0.0215 g of ammonium persulfate in water. iomi, other operating conditions similar to those in the fifth embodiment, the obtained conductive composite particle powder was ground and pressed into a tablet, and the measured conductivity was 0i26 s / cm. 26 l235387 In the ninth implementation of one of the present invention In the example, the aniline monomer solution was changed to 9 · 18 // 1 and the aqueous solution containing 00258 g of persulfuric acid solution iomi, and other operating conditions were the same as those in the fifth embodiment. The obtained conductive composite particle powder was ground and pressed. The measured conductivity was 0.157 s / cm. In one tenth embodiment of the present invention, the aniline monomer solution was changed to 10 ml with an aqueous solution containing 0.043 g of ammonium persulfate, and the others were the same as the fifth embodiment. The operating conditions of the example, the obtained conductive composite particle powder was ground and pressed into a tablet, and the measured conductivity was 0162 s / cm. In an eleventh embodiment of the present invention, the aniline monomer solution was changed to 24.8 // 1 and an aqueous solution containing 0.0688 g of ammonium persulfate 1〇 1. Other operating conditions are the same as those in the fifth embodiment. The obtained conductive composite particle powder is ground and pressed into a tablet, and the measured conductivity is Q145 S / cm. In a twelfth embodiment of the present invention, the change is changed. The aniline monomer solution was 30.6 // 1 and 0.086 g of an ammonium persulfate aqueous solution 1 (3 guab. The other operating conditions were the same as those in the fifth embodiment. The conductive composite particle powder obtained was ground and pressed into tablets. The electrical conductivity is 0 115 s / cm. In a twelfth embodiment of the present invention, the anionic surfactant is changed to an aqueous solution containing 0.055 g of sodium tetradecyi sUlfonate. Mi, aniline monomer solution is 9 · 18 / ^ and 0. 0258 grams of ammonium persulfate aqueous solution ι〇m Bu other operating conditions as in the fifth embodiment, the resulting conductivity is 27! 235387 particles of powder after grinding After being thinned, the tablet was measured to have a conductivity of 1,0 6 S / cm. In a fourteenth embodiment of the present invention, the aniline monomer solution * is changed to 6.12 "; and the aqueous solution containing 0.0172 g of an ammonium persulfate solution is 0 'ml, and other operating conditions are the same as those of the fifth embodiment. The obtained conductive composite particle powder was ground and pressed into a tablet, and the measured conductivity was 2.69x1 ()-2 S / cm. In the above-mentioned embodiments of the present invention, the present invention discloses a kind of stable electrical conductivity. ± Composite particles and the method for forming the same, the present invention can use at least one water-soluble ionic stabilizer to stabilize the first structure having at least one non-conductive polymer in an aqueous phase system, and can also perform a polymerization reaction in an aqueous phase medium. To form a second sigma structure with at least one conductive polymer, this process step is quite simple and can be performed in an aqueous phase system, so there are no disadvantages such as solvent-free volatile and pollution. In addition, the present invention opens the way to solution Casting method or molten die-casting method is used to make conductive films or directly coated on non-conductive substrates to make conductive substrates. It can be seen that this technology can be applied to conductive, metallized, anti-electromagnetic interference, Manufacture of materials and components with antistatic properties, such as: light-emitting diodes, conductive electrodes, anti-corrosive coatings, discolored windows, capacitors, etc. Therefore, the invention can meet economic benefits and industrial applicability. As mentioned above, the present invention discloses a conductive composite particle, a method for forming the same, and an application thereof. The conductive composite particle includes a first structure having 28 to 235 387, a non-conductive polymer, and a vibrating ancient eight, The second structure of the W-guided knife and at least one ionic component refers to a μ. This ionizer further includes an ionic surfactant and a polyelectrolyte. In addition, the present invention also discloses a method for forming conductive composite particles. And: Application. Obviously, according to the description in the above embodiment, the present invention. + The amendments and differences of the evening. Therefore, it needs to be understood within the scope of the appended claims. In addition to the above detailed description, the present invention It can also be widely implemented in other embodiments. The above are only the present invention, and the preferred embodiments are not used to limit the patent application of the present invention. Scope: Any other equivalent changes or modifications made without departing from the spirit of the invention disclosed in the present invention should be included in the scope of the patent application described below.
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