US3924050A - Dielectric layer composition - Google Patents
Dielectric layer composition Download PDFInfo
- Publication number
- US3924050A US3924050A US37484773A US3924050A US 3924050 A US3924050 A US 3924050A US 37484773 A US37484773 A US 37484773A US 3924050 A US3924050 A US 3924050A
- Authority
- US
- United States
- Prior art keywords
- paper
- volume
- dielectric
- vinyl
- epoxy
- 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
- 239000000203 mixture Substances 0.000 title abstract description 11
- 239000003822 epoxy resin Substances 0.000 claims abstract description 14
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 14
- 239000004593 Epoxy Substances 0.000 claims abstract description 13
- 229920001577 copolymer Polymers 0.000 claims abstract description 13
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000000576 coating method Methods 0.000 claims description 22
- 239000011248 coating agent Substances 0.000 claims description 16
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 5
- 239000000049 pigment Substances 0.000 abstract description 13
- 239000000178 monomer Substances 0.000 abstract description 3
- 229920000642 polymer Polymers 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 230000014759 maintenance of location Effects 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000003801 milling Methods 0.000 description 3
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- -1 methyl ethacrylate Chemical compound 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
- XHAFIUUYXQFJEW-UHFFFAOYSA-N 1-chloroethenylbenzene Chemical compound ClC(=C)C1=CC=CC=C1 XHAFIUUYXQFJEW-UHFFFAOYSA-N 0.000 description 1
- RCSKFKICHQAKEZ-UHFFFAOYSA-N 1-ethenylindole Chemical compound C1=CC=C2N(C=C)C=CC2=C1 RCSKFKICHQAKEZ-UHFFFAOYSA-N 0.000 description 1
- OGMSGZZPTQNTIK-UHFFFAOYSA-N 1-methyl-2-prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1C OGMSGZZPTQNTIK-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- DPYJMQGTOTVJBV-UHFFFAOYSA-N 2,2-difluoroethenylbenzene Chemical class FC(F)=CC1=CC=CC=C1 DPYJMQGTOTVJBV-UHFFFAOYSA-N 0.000 description 1
- PRAMZQXXPOLCIY-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethanesulfonic acid Chemical compound CC(=C)C(=O)OCCS(O)(=O)=O PRAMZQXXPOLCIY-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- WHBAYNMEIXUTJV-UHFFFAOYSA-N 2-chloroethyl prop-2-enoate Chemical compound ClCCOC(=O)C=C WHBAYNMEIXUTJV-UHFFFAOYSA-N 0.000 description 1
- OYUNTGBISCIYPW-UHFFFAOYSA-N 2-chloroprop-2-enenitrile Chemical compound ClC(=C)C#N OYUNTGBISCIYPW-UHFFFAOYSA-N 0.000 description 1
- KMMADNSYQPKZIM-UHFFFAOYSA-N 2-chloropropyl prop-2-enoate Chemical compound CC(Cl)COC(=O)C=C KMMADNSYQPKZIM-UHFFFAOYSA-N 0.000 description 1
- DBWWINQJTZYDFK-UHFFFAOYSA-N 2-ethenyl-1,4-dimethylbenzene Chemical class CC1=CC=C(C)C(C=C)=C1 DBWWINQJTZYDFK-UHFFFAOYSA-N 0.000 description 1
- MZNSQRLUUXWLSB-UHFFFAOYSA-N 2-ethenyl-1h-pyrrole Chemical compound C=CC1=CC=CN1 MZNSQRLUUXWLSB-UHFFFAOYSA-N 0.000 description 1
- BWLBGMIXKSTLSX-UHFFFAOYSA-N 2-hydroxyisobutyric acid Chemical compound CC(C)(O)C(O)=O BWLBGMIXKSTLSX-UHFFFAOYSA-N 0.000 description 1
- FCYVWWWTHPPJII-UHFFFAOYSA-N 2-methylidenepropanedinitrile Chemical compound N#CC(=C)C#N FCYVWWWTHPPJII-UHFFFAOYSA-N 0.000 description 1
- BYDRTKVGBRTTIT-UHFFFAOYSA-N 2-methylprop-2-en-1-ol Chemical compound CC(=C)CO BYDRTKVGBRTTIT-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical class CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 241001312297 Selar Species 0.000 description 1
- 229920003365 Selar® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- AUNAPVYQLLNFOI-UHFFFAOYSA-L [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O Chemical compound [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O AUNAPVYQLLNFOI-UHFFFAOYSA-L 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 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
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- OMRRUNXAWXNVFW-UHFFFAOYSA-N fluoridochlorine Chemical compound ClF OMRRUNXAWXNVFW-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- HILCQVNWWOARMT-UHFFFAOYSA-N non-1-en-3-one Chemical compound CCCCCCC(=O)C=C HILCQVNWWOARMT-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- CYFIHPJVHCCGTF-UHFFFAOYSA-N prop-2-enyl 2-hydroxypropanoate Chemical compound CC(O)C(=O)OCC=C CYFIHPJVHCCGTF-UHFFFAOYSA-N 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/002—Inhomogeneous material in general
- H01B3/006—Other inhomogeneous material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/04—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09D127/08—Homopolymers or copolymers of vinylidene chloride
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/0202—Dielectric layers for electrography
- G03G5/0205—Macromolecular components
- G03G5/0208—Macromolecular components obtained by reactions only involving carbon-to-carbon unsatured bonds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/0202—Dielectric layers for electrography
- G03G5/0205—Macromolecular components
- G03G5/0211—Macromolecular components obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/0202—Dielectric layers for electrography
- G03G5/0217—Inorganic components
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
- Y10T428/31895—Paper or wood
- Y10T428/31906—Ester, halide or nitrile of addition polymer
Definitions
- Electrographic paper for use in electrostatic printing
- said paper being formulated to look like ordinary pal0 per, consists of a paper substrate generally made conductive by the addition of electroconductive resins or salts, on the top of which is placed a highly resistive dielectric resin coating.
- these papers contain a pigment, the purpose of which is to reduce the gloss of the polymer coating and to give the paper a flat, mattetype finish.
- the resulting paper can be of any size, depending upon the requirements of the machine.
- the paper is passed through an electrographic printer. Voltage in the range of 500-900 volts.is applied across the dielectric coating.
- One process has an electrode making contact with the electroconductive substrate, and the other electrode, consisting of styli which are selectively activated by programmed impulses, is in proximity with, but not touching, the dielectric coating. An electrical discharge occurs across the air gap, resulting in an electrostatic image on the surface of the paper.
- An alternative process charges the dielectric layer through one stylus, with the return path through another electrode on the same side of the paper.
- the dielectric layer functions as a charged capacitor, the charged paper then being passed through a toner containing oppositely charged particles. The particles adhere to the electrostatic image, resulting in a visible print.
- dielectric materials which, when coated on paper, will accept a static charge and produce a toned image at about 50% room humidity. Any fairly good dielectric will hold sufficient charge long enough to be toned out in a few minutes to produce'a visible print.
- the conductivity of the base sheet must be provided solely by the electroconductive resin with which it is impregnated. Conductivity of the base sheet determines the time required to transfer charge to the dielectric.
- the dielectric coating must be capable of being charged in a matter of about 50 microseconds. As .the humidity goes up to 80 percent and higher, other problems become paramount. For instance, the papers begin to exhibit curl problems and the charge leaks off and through the paper much more quickly. In addition, parts of the dielectric coating lose their dielectric strength and break down at voltage levels which are inadequate for printing.
- Dielectric coatings have now been found which have desirable properties when said coatings and their associated substrate are exposed to relatively high humidities, i.e., above about 50%.
- the coatings of this invention exhibit desirable dielectric properties under said conditions, i.e., they exhibit l good charging characteristics, (2) good charge retention characteristics, and (3) the ability to withstand changes in the dimensions of the substrate.
- the coatings of this invention consist essentially of 15 to 85 volume preferably 32 to 58%, ofa copolymer of vinylidene chloride and at least one other olefinically unsaturated comonomer polymerizable therewith; 8 to 77 volume 70, preferably 24 to 50%, of an epoxy resin having an epoxy equivalent weight of about 400 to 60,000; and, optionally, 0 to 42 volume preferably 10 to 25%, of a pigment.
- the coating may be placed on one or both sides of an electrographic paper by known techniques, i.e., impregnating, padding, dipping, spraying, coating, or the like, in an amount effective as a dielectric layer, resulting in papers suitable for use in electrostatic printing processes.
- a coat weight of about 1 to 15 pounds per ream (3,000 ft. preferably about 3 to 6 pounds per ream, .is generally suitable.
- the approximate optimum volume ratio of components for use herein at high relative humidities, i.e., above about 50%, is about 49%copolymer, about 37% epoxy resin and about 14% pigment.
- Copolymers suitable for the practice of the present invention include copolymers of vinylidene chloride containing at least about weight percent, preferably about 80%, but less than about 96% vinylidene chloride and at least one other olefinically unsaturated monomer copolymerisable therewith.
- Examples include 0-, mand p-methyl styrenes; alpha-methyl styrene; 2,3-,2,4- and 2,5- dimethyl styrenes; alpha-chlorostyrene; alpha-ethyl styrene; o-, mand p-bromo-, chloroor fluorostyrenes; isopropenyl toluene; 2,3-, 2,4- and 2,5-dichloro-, dibromo-and difluorostyrenes; and the like.
- vinyl naphthalene methacrylonitrile; acrylonitrile; 2-chloroacrylonitrile; vinylchloride; acrylate and alkylacrylate esters, such as methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, Z-ethyI-hexylacrylate, dodecyl acrylate, 2-chloroethyl acrylate, Z-hydroxy-ethyl acrylate, Z-hydroxy-propyl acrylate, 2-chloropropyl acrylate, 2,2-dichloro-isopropyl acrylate, phenyl acrylate, cyclohexyl acrylate, methyl alpha-chloroacrylate, methyl methacrylate, ethyl methacrylate, 2-sulfo-ethyl methacrylate and methyl ethacrylate; vinylidene cyanide; vinyl esters, such as
- vinyl ethers such as vinyl methyl ether and vinyl isobumagnesium silicate talc, aluminum silicate china clay, tyl ether; vinyl ketones. such as vinyl'methyl ketone, mica. bentonite, wollastonite and lorite), lithopone, vinyl hexyl ketone and methyl isopropenyl ketone; iso- Zinc sulfide. antimony oxide. barium sulfate. calcium butylene; l-butene; vinylidene halides. such as vinyli- 5 carbonate. ground limestone. toluidine red toner, dene chlorofluoride; N-vinyl compounds. such as N- hansa yellow. chrome yellow.
- phthalocyanine green or vinyl pyrrole N-vinyl carbazole. N-vinyl indole and N- blue, molybdate orange, dinitraline orange toner. carvinyl succinimide; acrolein. methacrolein; acrylamide: bon black. and the like.
- Other pigments which could be methacrylamide; N-methylol acrylamide; allyl comsubstituted for the above will be obvious to those in the pounds. such as allyl alcohol, methallyl alcohol. allyl l0 coating arts.
- Lithopone is the preferred pigment for use acetate. allyl methacrylate, allyl lactate. allyl alphain the dielectric coating when a pigment is used.
- the above coatings may suitably be prepared by dis- Copolymers which are suitable herein haveamolecusolving the copolymer and epoxy resin, in any selar weight which is described by a-relative viscosity of quence. in a suitable solvent in the desired ratio.
- a pigbetween about 1.2 and 3.5, preferably 1.6 to 3.0, for a ment, if desired, may be dispersed into the solution by 1% tetrahydrofuran solution at C as determined by known techniques. such as sand milling. Ambient con- ASTM Test ,Dl243-60. ditions are generally suitable "for the above process.
- Preferred copolymers include those which are 75 to Suitable solvents include ketones, such as methyl 95% vinylidene chloride and 5 to 257r vinyl chloride or ethyl ketone, acetone, cyclohexanone and isophorone;
- ketones such as methyl 95% vinylidene chloride and 5 to 257r vinyl chloride or ethyl ketone, acetone, cyclohexanone and isophorone;
- acrylonitrile. and tetrahydrofuran, dimethylformamide, ethyl ace- Suitable epoxy resins are those which have an epoxy tate, and the like.
- lithopone pigment was then added, and sand-milled (20-30 mesh milling sand) at 3700 RPM for about 15 minutes.
- the sand was separated by filtering the coating/milling sand mixture through a conicalpaper paint filter.
- Q i H or The above mixture was then applied to a conductivebase paper of 133 megohms/ I] by the use of a wire- 0 wound rod, typically a No. 18 rod. Howeventhe rod size and solids content of the mixture were both varied to control the holdout from the paper and the coating weight.
- each X is Cl or Br; Films were used with coating weights of from 3 lbs. to each n is 0 to 2; and m is about 1 to 210. l4 lbs/ream.
- Q is 2.3-epoxypropyl and the epoxy equivasupply had the negative lead connected to the test plate lent weight is between about 800 and 6,000. and the positive lead connected to a piece of foil.
- dielectric coatings are suitable herein.
- dielectric side facing the plate Intimate contact example. the following may be used: white leads (such was achieved by the use of a rubber roller.
- B. 8 to 77 volume 7 of an epoxy resin having an epoxy equivalent weight of about 400 to 60,000, said epoxy resin being of the formula O x n x n X x n CH CHCH O Z OCH iHCH O Z 0Q.
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Abstract
There is disclosed a paper which is suitable for use in electrostatic printing, said paper being coated on at least one side with a dielectric composition, which is useful particularly at relatively high humidities, consisting of 15 to 85 volume % of a copolymer of vinylidene chloride and at least one other olefinically unsaturated monomer, 8 to 77 volume % of an epoxy resin having an epoxy equivalent weight between 400 and 60,000, and, optionally, 0 to 42 volume % of a pigment.
Description
United States Patent Camp et al. Dec. 2, 1975 [5 DIELECTRIC LAYER COMPOSITION 3.110.621 11/1963 Doggett ct al. 117/155 UA 3,l83,28l 5/1965 Clemens 260/837 R [75] lnvemors- Camly" -Q Lvermorer 3.236.683 2/1966 Berenbaum 6:61 260/836 Robert Lmdblom Walnut Creek- 3.385.730 5/l968 Relph 117/155 UA both of Calif.
[73] Assignee: The Dow Chemical Company, Primary E.t'am1'nerWilliam D. Martin Midland, Mich. Assistant Examiner-Janyce A. Bell [22] Filed June 29 1973 Attorney, Agent. or Firm.l. Roger Lochhead; Gary D. Street {21] App]. No.: 374,847 4 Related US. Application Data 5 ABSTRACT 1 2 -32 Ser No 173299 Aug 197] Pat No There 1s dlsclosed a paper whlch 1s su1table for use 1n electrostatic printing, said paper being coated on at [52] Cl. 428/413; 427/121. 428/514 least one side with a dielectric composition. which is 511 Int. Cl .f. 33121 27/38 useful Particularly relatively high humidifies- [58] Field of Search 260/41 R. 83-6 837- sisting of 3 volume of a copmymer of vinyl 117/223, 155 UA, 155 R, 61 U2 161 dene chloride and at least one other olefinically unsat- 161/184 25 urated monomer, 8 to 77 volume 71 of an epoxy resin having an epoxy equivalent weight between 400 and [56] References cued 60,000. and. optionally. 0 to 42 volume of a pig- UNITED STATES PATENTS 3,008,914 ll/l96l Fry 260/837 CA Claim, N0 Drawings DIELECTRIC LAYER COMPOSITION This is a divisional application of application Ser. No. 173,299, filed Aug. 19, 1971, now US. 3,779,982.
BACKGROUND OF THE INVENTION Electrographic paper for use in electrostatic printing,
said paper being formulated to look like ordinary pal0 per, consists of a paper substrate generally made conductive by the addition of electroconductive resins or salts, on the top of which is placed a highly resistive dielectric resin coating. Generally these papers contain a pigment, the purpose of which is to reduce the gloss of the polymer coating and to give the paper a flat, mattetype finish. The resulting paper can be of any size, depending upon the requirements of the machine.
In a typical printing process, the paper is passed through an electrographic printer. Voltage in the range of 500-900 volts.is applied across the dielectric coating. One process has an electrode making contact with the electroconductive substrate, and the other electrode, consisting of styli which are selectively activated by programmed impulses, is in proximity with, but not touching, the dielectric coating. An electrical discharge occurs across the air gap, resulting in an electrostatic image on the surface of the paper.
An alternative process charges the dielectric layer through one stylus, with the return path through another electrode on the same side of the paper.
The dielectric layer functions as a charged capacitor, the charged paper then being passed through a toner containing oppositely charged particles. The particles adhere to the electrostatic image, resulting in a visible print.
There are many dielectric materials which, when coated on paper, will accept a static charge and produce a toned image at about 50% room humidity. Any fairly good dielectric will hold sufficient charge long enough to be toned out in a few minutes to produce'a visible print.
But when the coated papers are run through high speed printers (5800 lines per minute) and when the humidity to which the paper is subjected begins to vary over a range of to 85 percent, each component of the electrographic system begins to have critical requirements.
At low humidity the conductivity of the base sheet must be provided solely by the electroconductive resin with which it is impregnated. Conductivity of the base sheet determines the time required to transfer charge to the dielectric. The dielectric coating must be capable of being charged in a matter of about 50 microseconds. As .the humidity goes up to 80 percent and higher, other problems become paramount. For instance, the papers begin to exhibit curl problems and the charge leaks off and through the paper much more quickly. In addition, parts of the dielectric coating lose their dielectric strength and break down at voltage levels which are inadequate for printing.
Past experience has shown that many soft resins, such as vinylidene chloride copolymers, while they do not curl, will not receive and maintain an electrical charge under high humidity conditions. On the other hand, while many hard resins, such as epoxy resins, will receive and maintain a charge, they exhibit excessive curl under these conditions.
SUMMARY OF THE INVENTION Dielectric coatings have now been found which have desirable properties when said coatings and their associated substrate are exposed to relatively high humidities, i.e., above about 50%.
The coatings of this invention exhibit desirable dielectric properties under said conditions, i.e., they exhibit l good charging characteristics, (2) good charge retention characteristics, and (3) the ability to withstand changes in the dimensions of the substrate.
The coatings of this invention consist essentially of 15 to 85 volume preferably 32 to 58%, ofa copolymer of vinylidene chloride and at least one other olefinically unsaturated comonomer polymerizable therewith; 8 to 77 volume 70, preferably 24 to 50%, of an epoxy resin having an epoxy equivalent weight of about 400 to 60,000; and, optionally, 0 to 42 volume preferably 10 to 25%, of a pigment.
The coating may be placed on one or both sides of an electrographic paper by known techniques, i.e., impregnating, padding, dipping, spraying, coating, or the like, in an amount effective as a dielectric layer, resulting in papers suitable for use in electrostatic printing processes. For instance, a coat weight of about 1 to 15 pounds per ream (3,000 ft. preferably about 3 to 6 pounds per ream, .is generally suitable. The approximate optimum volume ratio of components for use herein at high relative humidities, i.e., above about 50%, is about 49%copolymer, about 37% epoxy resin and about 14% pigment.
DETAILED DESCRIPTION OF THE INVENTION Copolymers suitable for the practice of the present invention include copolymers of vinylidene chloride containing at least about weight percent, preferably about 80%, but less than about 96% vinylidene chloride and at least one other olefinically unsaturated monomer copolymerisable therewith.
Among the myriad of suitable ethylenic comonomers are substituted and unsubstituted styrenes of the formula i=CH wherein each R and R is, independently, I-I, Cl, Br, F or a straight or branched-chain alkyl group of up to 8 carbon atoms (such as methyl, propyl, butyl or octyl), and n is 0 to 5. Examples include 0-, mand p-methyl styrenes; alpha-methyl styrene; 2,3-,2,4- and 2,5- dimethyl styrenes; alpha-chlorostyrene; alpha-ethyl styrene; o-, mand p-bromo-, chloroor fluorostyrenes; isopropenyl toluene; 2,3-, 2,4- and 2,5-dichloro-, dibromo-and difluorostyrenes; and the like.
Also suitable are vinyl naphthalene; methacrylonitrile; acrylonitrile; 2-chloroacrylonitrile; vinylchloride; acrylate and alkylacrylate esters, such as methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, Z-ethyI-hexylacrylate, dodecyl acrylate, 2-chloroethyl acrylate, Z-hydroxy-ethyl acrylate, Z-hydroxy-propyl acrylate, 2-chloropropyl acrylate, 2,2-dichloro-isopropyl acrylate, phenyl acrylate, cyclohexyl acrylate, methyl alpha-chloroacrylate, methyl methacrylate, ethyl methacrylate, 2-sulfo-ethyl methacrylate and methyl ethacrylate; vinylidene cyanide; vinyl esters, such as vinyl acetate, vinyl chloroacetate, vinyl propio- (iii nate, vinyl butyrate, vinyl laurate and vinyl stearate; CaSO silicas (such as amorphous. diatomaceous. vinyl ethers, such as vinyl methyl ether and vinyl isobumagnesium silicate talc, aluminum silicate china clay, tyl ether; vinyl ketones. such as vinyl'methyl ketone, mica. bentonite, wollastonite and lorite), lithopone, vinyl hexyl ketone and methyl isopropenyl ketone; iso- Zinc sulfide. antimony oxide. barium sulfate. calcium butylene; l-butene; vinylidene halides. such as vinyli- 5 carbonate. ground limestone. toluidine red toner, dene chlorofluoride; N-vinyl compounds. such as N- hansa yellow. chrome yellow. phthalocyanine green or vinyl pyrrole. N-vinyl carbazole. N-vinyl indole and N- blue, molybdate orange, dinitraline orange toner. carvinyl succinimide; acrolein. methacrolein; acrylamide: bon black. and the like. Other pigments which could be methacrylamide; N-methylol acrylamide; allyl comsubstituted for the above will be obvious to those in the pounds. such as allyl alcohol, methallyl alcohol. allyl l0 coating arts. Lithopone is the preferred pigment for use acetate. allyl methacrylate, allyl lactate. allyl alphain the dielectric coating when a pigment is used. hydroxyisobutyrate. and allyl acrylate; and the like. The above coatings may suitably be prepared by dis- Copolymers which are suitable herein haveamolecusolving the copolymer and epoxy resin, in any selar weight which is described by a-relative viscosity of quence. in a suitable solvent in the desired ratio. A pigbetween about 1.2 and 3.5, preferably 1.6 to 3.0, for a ment, if desired, may be dispersed into the solution by 1% tetrahydrofuran solution at C as determined by known techniques. such as sand milling. Ambient con- ASTM Test ,Dl243-60. ditions are generally suitable "for the above process.
Preferred copolymers include those which are 75 to Suitable solvents include ketones, such as methyl 95% vinylidene chloride and 5 to 257r vinyl chloride or ethyl ketone, acetone, cyclohexanone and isophorone;
acrylonitrile. and tetrahydrofuran, dimethylformamide, ethyl ace- Suitable epoxy resins are those which have an epoxy tate, and the like.
equivalent weight of about 400 to 60.000 and are genocmlHCHp wherein each Z is a chemical bond, O. S. E l
-S S*' To 160 ml. of methyl ethyl ketone in a wide-mouth bottle equipped with a magnetic stirrer was added 40 0 f gm. of a copolymer of 80% vinylidene chloride and u I 20% of acrylonitrile, said copolymer having relative a viscosity of 2.57 in a 1% solution of tetrahydrofuran at 25C. The solution was stirred for one hour, and then r 10 gm. of an epoxy resin of the above formula'wherein CH2 or n is 0, Z is isopropylidene and the epoxy equivalent 40 weight is about 1800, was added. the stirring continued for another hour. 40 gm. of lithopone pigment was then added, and sand-milled (20-30 mesh milling sand) at 3700 RPM for about 15 minutes. The sand was separated by filtering the coating/milling sand mixture through a conicalpaper paint filter. Q i H or The above mixture was then applied to a conductivebase paper of 133 megohms/ I] by the use of a wire- 0 wound rod, typically a No. 18 rod. Howeventhe rod size and solids content of the mixture were both varied to control the holdout from the paper and the coating weight. each X is Cl or Br; Films were used with coating weights of from 3 lbs. to each n is 0 to 2; and m is about 1 to 210. l4 lbs/ream. Commercial films are typically 5 These resins are generally formed by the reaction, in lb./ream. but lab samples are usually less perfect due to the presence ofa suitable catalyst. of a bisphenol and a batch-wise coating, and somewhat heavier films were diglycidyl ether of a bisphenol or an epihalohydrin in a necessary to achieve comparable dielectric strength ratio such that a product with an epoxy equivalent and charge retention. weight of about 400 to 60,000 is formed. this mode of The samples were evaluated by charging the dielecpreparation being well known to the art. tric film with 600 volts against anetched halftone mag- Preferred epoxy resins are those wherein Z is isopronesium test plate. A high impedance 600 voltpower pylidene. Q is 2.3-epoxypropyl and the epoxy equivasupply had the negative lead connected to the test plate lent weight is between about 800 and 6,000. and the positive lead connected to a piece of foil. The Pigments known to the art to be useful when incorpopaper was interposed between the plate and the foil,
rated into dielectric coatings are suitable herein. As an the dielectric side facing the plate. Intimate contact example. the following may be used: white leads (such was achieved by the use of a rubber roller.
as basic carbonates. sulfates and silicates). zinc oxides The electrostatic image thus achieved was converted (such as acicular. nodular and 35% leaded). titanium into an optical image by the use of a commercially dioxides (such as rutile. anatasev and 30% TiO /7c available liquid toner.
Charge acceptance and retention was measured by a Most Associates Stati-Tester. To measure charge retention, the charged paper was placed in the machine where it was given a charge by corona discharge. Sub- 6 Test prints were also visually inspected, compared and rated Excellent (E), Good (G), Fair (F) or Poor (P) according to their uniformity of toning.
Each test was carried out on a print which had been sequent to the charging period, the machine measured 5 immediately toned (0 min.) and toned minutes after the surface charge (Vo) with an electrometer. The macharging (30 min. and at 50 and 80% relative humidichine then measured surface charge 2 minutes later ties. However, regarding the results below. it is to be (V). The paper was thusly tested under ambient humidunderstood that the comparisons must be made bearing ity conditions (-7c) and at 85% relative humidity. in mind the differences in coat weights. Lithopone was The table below summarizes this data for various 10 used as pigment, the amounts being shown in the table.
Print Quality RH. 80% R.H. Density Unifomity Density L'niformity Vol. 7t Vol. 71 Vol. "/1 Coat 0 30 30 0 30 0 30 Polymer Epoxy Pigment Wcight Min Min Min Min Min Min Min Min 1. 73 0 27 7.7 0.8 0.4 E E 0.5 0.2 P P 2. 51 25 25 8.8 0.9 0.4 E E 0.8 0.2 G F 3. 43 32 25 8.9 1.2 0.7 E E 0.6 0.5 G F 4. 32 44 24 (1.7 1.2 0.7 E E 0.7 0.4 F P 5. 22 23 7.5 1.0 0.7 c; o 0.7 0.2 P P e. 0 79 21 7.5 0.7 0.6 P F 0.2 0.1 P P coat weights and different ratios of polymer and epoxy. It is apparent from the above that, particularly at high The pigment used was lithopone, the amount used (i.e., humidities, the blends of polymer and epoxy being shown in the table. The coat weights given are of this invention are superior to either alone. approximate, it being understood that variations in coat 25 We claim: weight will result in variations in results. I. A paper suitable for use in electrostatic printing TABLE I.
5 lbs/Ream" 8 lbs/Ream" Ex. v01. 71 W1. /1 v01. /1 35% RH. 8571 R.H. 35% RH. 35% RH. No. Polymer Epoxy Pigment V,, V,,/V V,, \/',,/V V.,/V '..l\'
"coat-weight of dielectric film Regarding Table l, the most desired ratio of V,,/V is processes comprising an electrographic paper coated 1, showing perfect charge retention. However, it is on at least one side with an effective amount of a diclear that various blends of polymers and epoxy resins 40 electric coating composition consisting essentially of are superior in both initial charging and charge reten- A. 15 to 85 volume 7: of a copolymer of 70 to 96 tion over either alone, it being understood that optiweight vinylidene chloride, the remainder being mum ratios of the two may easily be determined for at least one other olefmically unsaturated comonovarious humidity conditions and coat weights. mer polymerizable therewith, said copolymer hav- The ability of a dielectric coating to accept and retain 45 ing a molecular weight described by a relative visa charge ultimately is judged by print contrast on a toned sheet. The contrasts of the dielectric composition of the instant invention was measured by a microscope, which allowed small areas 1 .4 mm to be observed. A light meter was used to measure the reflected cosity of between about 1.2 and 3.5 for a 1% tetrahydrofuran solution at 25C.;
B. 8 to 77 volume 7: of an epoxy resin having an epoxy equivalent weight of about 400 to 60,000, said epoxy resin being of the formula O x n x n X x n CH CHCH O Z OCH iHCH O Z 0Q.
Claims (1)
1. A PAPER SUITABLE FOR USE IN ELECTROSTATIC PRINTING PROCESSES COMPRISING AN ELECTROGRAPHIC PAPER COATED ON AT LEAST ONE SIDE WITH AN EFFECTIVE AMOUNT OF A DIELECTRIC COATING POSITION CONSISTING ESSENTIALLY OF A. 15 TO 85 VOLUME % OF A COPOLYMER OF 70 TO 96 WEIGHT % VINYLIDENE CHLORIDE, THE REMAINDER BEING AT LEAST ONE OTHER OLEFINICALLY UNSATURATED COMONOMER POLYMERIZABLE THEREWITH, SAID COMPLYMER HAVING A MOLECULAR WEIGHT DESCRIBED BY A RELATIVE VISCOSITY OF BETWEEN ABOUT 1.2 AND 3.5 FOR A 1% TETRAHYDROFURAN SOLUTION AT 25*C.; B. 8 TO 77 VOLUME % OF AN EPOXY RESIN HAVING AN EPOXY EQUIVALENT WEIGHT OF ABOUT 400 TO 60,000, SAID EPOXY RESIN BEING OF THE FORMULA
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37484773 US3924050A (en) | 1971-08-19 | 1973-06-29 | Dielectric layer composition |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17329971A | 1971-08-19 | 1971-08-19 | |
| US37484773 US3924050A (en) | 1971-08-19 | 1973-06-29 | Dielectric layer composition |
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| US3924050A true US3924050A (en) | 1975-12-02 |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3975305A (en) * | 1975-06-27 | 1976-08-17 | Nalco Chemical Company | Ionene conductive polymers and resulting electrographic printing bases |
| US4145478A (en) * | 1977-07-28 | 1979-03-20 | Desoto, Inc. | Calcium oxide or hydroxide to improve the charge acceptance of electrographic dielectric resins |
| US4204971A (en) * | 1977-07-28 | 1980-05-27 | Desoto, Inc. | Calcium oxide or hydroxide to improve the charge acceptance of electrographic dielectric resins |
| EP0818712A3 (en) * | 1989-11-17 | 1999-10-20 | Dai Nippon Printing Co., Ltd. | Electrostatic information-recording media and process for recording and reproducing electrostatic information |
| DE19848409A1 (en) * | 1998-10-21 | 2000-04-27 | Esselte Leitz Gmbh & Co Kg | Electrostatic and chargeable flat material with reduced water permeability has a paper core and a non-porous dielectric material layer(s) on its surface |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3008914A (en) * | 1958-10-06 | 1961-11-14 | Union Carbide Corp | Composition comprising an acrylic acid polymer and a polyglycidyl ether and products thereof |
| US3110621A (en) * | 1960-02-01 | 1963-11-12 | Warren S D Co | Electrostatic recording paper |
| US3183281A (en) * | 1961-07-19 | 1965-05-11 | Rohm & Haas | Stable self-catalyzing epoxy resin compositions |
| US3236683A (en) * | 1962-10-11 | 1966-02-22 | Thiokol Chemical Corp | Method of coating metal with a vinylidene chloride copolymer and polyepoxide reaction product and article produced thereby |
| US3385730A (en) * | 1964-04-01 | 1968-05-28 | Dick Co Ab | Writing medium for electrostatic printing |
-
1973
- 1973-06-29 US US37484773 patent/US3924050A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3008914A (en) * | 1958-10-06 | 1961-11-14 | Union Carbide Corp | Composition comprising an acrylic acid polymer and a polyglycidyl ether and products thereof |
| US3110621A (en) * | 1960-02-01 | 1963-11-12 | Warren S D Co | Electrostatic recording paper |
| US3183281A (en) * | 1961-07-19 | 1965-05-11 | Rohm & Haas | Stable self-catalyzing epoxy resin compositions |
| US3236683A (en) * | 1962-10-11 | 1966-02-22 | Thiokol Chemical Corp | Method of coating metal with a vinylidene chloride copolymer and polyepoxide reaction product and article produced thereby |
| US3385730A (en) * | 1964-04-01 | 1968-05-28 | Dick Co Ab | Writing medium for electrostatic printing |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3975305A (en) * | 1975-06-27 | 1976-08-17 | Nalco Chemical Company | Ionene conductive polymers and resulting electrographic printing bases |
| US4145478A (en) * | 1977-07-28 | 1979-03-20 | Desoto, Inc. | Calcium oxide or hydroxide to improve the charge acceptance of electrographic dielectric resins |
| US4204971A (en) * | 1977-07-28 | 1980-05-27 | Desoto, Inc. | Calcium oxide or hydroxide to improve the charge acceptance of electrographic dielectric resins |
| EP0818712A3 (en) * | 1989-11-17 | 1999-10-20 | Dai Nippon Printing Co., Ltd. | Electrostatic information-recording media and process for recording and reproducing electrostatic information |
| DE19848409A1 (en) * | 1998-10-21 | 2000-04-27 | Esselte Leitz Gmbh & Co Kg | Electrostatic and chargeable flat material with reduced water permeability has a paper core and a non-porous dielectric material layer(s) on its surface |
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