EP0004748B1 - Electrostatographic developer mixture and imaging process - Google Patents
Electrostatographic developer mixture and imaging process Download PDFInfo
- Publication number
- EP0004748B1 EP0004748B1 EP79300512A EP79300512A EP0004748B1 EP 0004748 B1 EP0004748 B1 EP 0004748B1 EP 79300512 A EP79300512 A EP 79300512A EP 79300512 A EP79300512 A EP 79300512A EP 0004748 B1 EP0004748 B1 EP 0004748B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- toner
- particles
- parts
- mixture
- 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
Links
- 239000000203 mixture Substances 0.000 title claims description 96
- 238000000034 method Methods 0.000 title claims description 26
- 230000008569 process Effects 0.000 title claims description 7
- 238000003384 imaging method Methods 0.000 title claims description 6
- 239000002245 particle Substances 0.000 claims description 146
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 43
- 239000011248 coating agent Substances 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 10
- 239000006229 carbon black Substances 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 239000011810 insulating material Substances 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 claims description 3
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 claims description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 150000002009 diols Chemical class 0.000 claims description 3
- 230000032050 esterification Effects 0.000 claims description 3
- 238000005886 esterification reaction Methods 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 3
- 229910000859 α-Fe Inorganic materials 0.000 claims description 3
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- FHESUNXRPBHDQM-UHFFFAOYSA-N diphenyl benzene-1,3-dicarboxylate Chemical compound C=1C=CC(C(=O)OC=2C=CC=CC=2)=CC=1C(=O)OC1=CC=CC=C1 FHESUNXRPBHDQM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 description 56
- 239000011347 resin Substances 0.000 description 32
- 229920005989 resin Polymers 0.000 description 32
- 239000012876 carrier material Substances 0.000 description 18
- -1 ethylene, propylene, butylene, isobutylene Chemical group 0.000 description 18
- 229920002554 vinyl polymer Polymers 0.000 description 16
- 238000011161 development Methods 0.000 description 15
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 15
- 108091008695 photoreceptors Proteins 0.000 description 13
- 238000002156 mixing Methods 0.000 description 10
- 239000007787 solid Substances 0.000 description 9
- 239000000049 pigment Substances 0.000 description 8
- 238000012546 transfer Methods 0.000 description 8
- 239000000975 dye Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000000969 carrier Substances 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 239000011162 core material Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 241000872198 Serjania polyphylla Species 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 2
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 2
- RCSKFKICHQAKEZ-UHFFFAOYSA-N 1-ethenylindole Chemical compound C1=CC=C2N(C=C)C=CC2=C1 RCSKFKICHQAKEZ-UHFFFAOYSA-N 0.000 description 2
- CTXUTPWZJZHRJC-UHFFFAOYSA-N 1-ethenylpyrrole Chemical compound C=CN1C=CC=C1 CTXUTPWZJZHRJC-UHFFFAOYSA-N 0.000 description 2
- UDJZTGMLYITLIQ-UHFFFAOYSA-N 1-ethenylpyrrolidine Chemical compound C=CN1CCCC1 UDJZTGMLYITLIQ-UHFFFAOYSA-N 0.000 description 2
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- WHBAYNMEIXUTJV-UHFFFAOYSA-N 2-chloroethyl prop-2-enoate Chemical compound ClCCOC(=O)C=C WHBAYNMEIXUTJV-UHFFFAOYSA-N 0.000 description 2
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000012644 addition polymerization Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- JLDSOYXADOWAKB-UHFFFAOYSA-N aluminium nitrate Chemical compound [Al+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O JLDSOYXADOWAKB-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 2
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical class O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical class C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 2
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 2
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 2
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 2
- 150000005673 monoalkenes Chemical class 0.000 description 2
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 2
- HILCQVNWWOARMT-UHFFFAOYSA-N non-1-en-3-one Chemical compound CCCCCCC(=O)C=C HILCQVNWWOARMT-UHFFFAOYSA-N 0.000 description 2
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 2
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 2
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical compound C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 description 1
- LEQDMTLZQXMITJ-UHFFFAOYSA-N 16,17,20,21-tetrazapentacyclo[12.10.0.03,12.05,10.015,22]tetracosa-1,3,5,7,9,11,13,15(22),16,18,20,23-dodecaene Chemical compound N1=NC=CN=NC=2C=CC=3C=C4C=C5C=CC=CC5=CC4=CC=3C=21 LEQDMTLZQXMITJ-UHFFFAOYSA-N 0.000 description 1
- IPXSAYARKMFWCP-UHFFFAOYSA-N 2,3,4-triphenyl-1h-pyrrole Chemical compound C=1NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C=1C1=CC=CC=C1 IPXSAYARKMFWCP-UHFFFAOYSA-N 0.000 description 1
- AXSVCKIFQVONHI-UHFFFAOYSA-N 2,3-bis(4-methoxyphenyl)-1-benzofuran-6-ol Chemical compound C1=CC(OC)=CC=C1C1=C(C=2C=CC(OC)=CC=2)C2=CC=C(O)C=C2O1 AXSVCKIFQVONHI-UHFFFAOYSA-N 0.000 description 1
- UKUVVAMSXXBMRX-UHFFFAOYSA-N 2,4,5-trithia-1,3-diarsabicyclo[1.1.1]pentane Chemical compound S1[As]2S[As]1S2 UKUVVAMSXXBMRX-UHFFFAOYSA-N 0.000 description 1
- QAHMKHHCOXNIHO-UHFFFAOYSA-N 2,4-diphenylquinazoline Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=CC=C2)C2=N1 QAHMKHHCOXNIHO-UHFFFAOYSA-N 0.000 description 1
- 229940054266 2-mercaptobenzothiazole Drugs 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- MLAJDFOBMYBISF-UHFFFAOYSA-N 4,5-diphenylimidazolidin-2-one Chemical compound N1C(=O)NC(C=2C=CC=CC=2)C1C1=CC=CC=C1 MLAJDFOBMYBISF-UHFFFAOYSA-N 0.000 description 1
- HJYSGEJLUSZCTF-UHFFFAOYSA-N 4,5-diphenylimidazolidine-2-thione Chemical compound N1C(S)=NC(C=2C=CC=CC=2)C1C1=CC=CC=C1 HJYSGEJLUSZCTF-UHFFFAOYSA-N 0.000 description 1
- NLWWHMRHFRTAII-UHFFFAOYSA-N 4-(1,3-benzoxazol-2-yl)-n,n-dimethylaniline Chemical compound C1=CC(N(C)C)=CC=C1C1=NC2=CC=CC=C2O1 NLWWHMRHFRTAII-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- LSZJZNNASZFXKN-UHFFFAOYSA-N 9-propan-2-ylcarbazole Chemical compound C1=CC=C2N(C(C)C)C3=CC=CC=C3C2=C1 LSZJZNNASZFXKN-UHFFFAOYSA-N 0.000 description 1
- LRSYZHFYNDZXMU-UHFFFAOYSA-N 9h-carbazol-3-amine Chemical compound C1=CC=C2C3=CC(N)=CC=C3NC2=C1 LRSYZHFYNDZXMU-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 240000000972 Agathis dammara Species 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 239000004859 Copal Substances 0.000 description 1
- 229920002871 Dammar gum Polymers 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- 241000782205 Guibourtia conjugata Species 0.000 description 1
- 241000082244 Ipomoea purga Species 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910001053 Nickel-zinc ferrite Inorganic materials 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 241001060310 Styracaceae Species 0.000 description 1
- 235000001361 Styrax officinalis Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241000364021 Tulsa Species 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 239000004110 Zinc silicate Substances 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 229940007424 antimony trisulfide Drugs 0.000 description 1
- NVWBARWTDVQPJD-UHFFFAOYSA-N antimony(3+);trisulfide Chemical compound [S-2].[S-2].[S-2].[Sb+3].[Sb+3] NVWBARWTDVQPJD-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- WBFMCDAQUDITAS-UHFFFAOYSA-N arsenic triselenide Chemical compound [Se]=[As][Se][As]=[Se] WBFMCDAQUDITAS-UHFFFAOYSA-N 0.000 description 1
- 229940052288 arsenic trisulfide Drugs 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- KVBYPTUGEKVEIJ-UHFFFAOYSA-N benzene-1,3-diol;formaldehyde Chemical compound O=C.OC1=CC=CC(O)=C1 KVBYPTUGEKVEIJ-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 229940116367 cadmium sulfide Drugs 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- LJLWNMFUZWUGPO-UHFFFAOYSA-N calcium strontium disulfide Chemical compound [S--].[S--].[Ca++].[Sr++] LJLWNMFUZWUGPO-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 239000012612 commercial material Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- PGWFQHBXMJMAPN-UHFFFAOYSA-N ctk4b5078 Chemical compound [Cd].OS(=O)(=O)[Se]S(O)(=O)=O PGWFQHBXMJMAPN-UHFFFAOYSA-N 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZZEMEJKDTZOXOI-UHFFFAOYSA-N digallium;selenium(2-) Chemical compound [Ga+3].[Ga+3].[Se-2].[Se-2].[Se-2] ZZEMEJKDTZOXOI-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- ANAGEECPKFGKEL-UHFFFAOYSA-N furan-2-carbaldehyde;phenol Chemical compound OC1=CC=CC=C1.O=CC1=CC=CO1 ANAGEECPKFGKEL-UHFFFAOYSA-N 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000006233 lamp black Substances 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
- PNHVEGMHOXTHMW-UHFFFAOYSA-N magnesium;zinc;oxygen(2-) Chemical compound [O-2].[O-2].[Mg+2].[Zn+2] PNHVEGMHOXTHMW-UHFFFAOYSA-N 0.000 description 1
- 229940002712 malachite green oxalate Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000007567 mass-production technique Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229960003671 mercuric iodide Drugs 0.000 description 1
- 229940101209 mercuric oxide Drugs 0.000 description 1
- YFDLHELOZYVNJE-UHFFFAOYSA-L mercury diiodide Chemical compound I[Hg]I YFDLHELOZYVNJE-UHFFFAOYSA-L 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- DUWGALKQOSBYKH-UHFFFAOYSA-N n-(9h-carbazol-3-yl)-1-phenylmethanimine Chemical compound C=1C=C2NC3=CC=CC=C3C2=CC=1N=CC1=CC=CC=C1 DUWGALKQOSBYKH-UHFFFAOYSA-N 0.000 description 1
- DWXAPYADWDBIII-UHFFFAOYSA-N n-[[4-(dimethylamino)phenyl]methylideneamino]benzamide Chemical compound C1=CC(N(C)C)=CC=C1C=NNC(=O)C1=CC=CC=C1 DWXAPYADWDBIII-UHFFFAOYSA-N 0.000 description 1
- BENSWQOUPJQWMU-UHFFFAOYSA-N naphthalene-1,4-dicarbonitrile Chemical compound C1=CC=C2C(C#N)=CC=C(C#N)C2=C1 BENSWQOUPJQWMU-UHFFFAOYSA-N 0.000 description 1
- WNDSQRGJJHSKCQ-UHFFFAOYSA-N naphthalene-1,5-dicarbonitrile Chemical compound C1=CC=C2C(C#N)=CC=CC2=C1C#N WNDSQRGJJHSKCQ-UHFFFAOYSA-N 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 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
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 229920006215 polyvinyl ketone Polymers 0.000 description 1
- 229920000131 polyvinylidene Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- PEFYPPIJKJOXDY-UHFFFAOYSA-J potassium;tetrachloroalumanuide Chemical compound [Al+3].[Cl-].[Cl-].[Cl-].[Cl-].[K+] PEFYPPIJKJOXDY-UHFFFAOYSA-J 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 229940051201 quinoline yellow Drugs 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- QXKXDIKCIPXUPL-UHFFFAOYSA-N sulfanylidenemercury Chemical compound [Hg]=S QXKXDIKCIPXUPL-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- XSMMCTCMFDWXIX-UHFFFAOYSA-N zinc silicate Chemical compound [Zn+2].[O-][Si]([O-])=O XSMMCTCMFDWXIX-UHFFFAOYSA-N 0.000 description 1
- 235000019352 zinc silicate Nutrition 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- UQMZPFKLYHOJDL-UHFFFAOYSA-N zinc;cadmium(2+);disulfide Chemical compound [S-2].[S-2].[Zn+2].[Cd+2] UQMZPFKLYHOJDL-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/0819—Developers with toner particles characterised by the dimensions of the particles
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/10—Developers with toner particles characterised by carrier particles
Definitions
- This invention relates to an electrostatographic developer mixture, and to an electrostatographic imaging process using the developer mixture.
- the mixture comprises finely-divided toner particles electrostatically clinging to the surface of carrier particles.
- the formation and development of images on the surface of photoconductive materials by electrostatic means is well-known.
- the basic electrostatographic process as taught by C. F. Carlson in U.S. Pat. No. 2,297,691, involves placing a uniform electrostatic charge on a photoconductive insulating layer, exposing the layer to a light-and-shadow image to dissipate the charge on the areas of the layer exposed to the light and developing the resulting electrostatic latent image by depositing on the image a finely-divided electroscopic material referred to in the art as "toner".
- One technique for developing an electrostatic latent image is the "magnetic brush” process as disclosed, for example, in U.S. Pat. No. 2,874,063.
- a developer material containing toner and magnetic carrier particles is carried by a magnet.
- the magnetic field on the magnet causes alignment of the magnetic carriers in a brush-like configuration.
- This magnetic brush is engaged with an electrostatic latent image-bearing surface and the toner particles are drawn from the brush to the electrostatic image by electrostatic attraction.
- Many other methods such as "touchdown” development as disclosed by C. R. Mayo in U.S. Pat. No. 2,895,847 are known for applying electroscopic particles to the electrostatic latent image to be developed.
- the image density may be improved by increasing the toner concentration in the developer mixture, undesirably high background toner deposition as well as increased toner impaction and agglomeration is encountered when the toner concentration in the developer mixture is excessive.
- the initial electrostatographic plate charge may be increased to improve the density of the deposited powder image, but the plate charge would ordinarily have to be excessively high in order to attract the electroscopic powder away from the carrier particle.
- Excessively high electrostatographic plate charges are not only undesirable because of the high power consumption necessary to maintain the electrostatographic plate at high potentials, but also because the high potential causes the carrier particles to adhere to the electrostatographic plate surface rather than merely roll across and off the electrostatographic plate surface.
- U.S. Patent 3,942,979 there is disclosed a developer mixture comprising classified toner materials having a particle size distribution wherein less than about 30% by number of the toner particles have an average particle size diameter of less than about 5 pm, about 25% of the particles have a diameter between about 8 ⁇ m and about 12 ⁇ m and less than about 5% by number of the toner particles have an average particle diameter greater than about 20 ⁇ m.
- the high surface area carrier materials have a specific surface of at least about 150 cm 2 /gram. It is also indicated therein that for cascade and magnetic brush development, the carrier particles generally have an average diameter between about 30 ⁇ m and 1000 ⁇ m, and between about 30 and about 250 ⁇ m respectively. In the case of magnetic brush development, the preferred carrier has a majority of the carrier particles in the range 74 to 105 ⁇ m.
- a developer mixture comprising toner particles and carrier particles, in which the carrier particles comprise a mixture of small and large particles.
- the toner particles are in the size range 5 to 20 ⁇ m, the small carrier particles from 1 to 25 ⁇ m and the large carrier particles from 15 to 200 ⁇ m. In a typical mixture, the toner particles range from 8 to 15 ⁇ m, with a main particle size of 10-11 pm.
- Most of the large carrier particles are from 30 to 80 ⁇ m in size with the most numerous size being 50-52 ⁇ m, and most of the small carrier particles are from 5 to 16 ⁇ m in size with the most numerous particle size being 15-16 ⁇ m.
- Present commercial magnetic brush development systems generally employ carrier particles that are approximately 100 ⁇ m in diameter. Toner particles employed with these carrier particles typically have a distribution of particle sizes that vary from 1 to 30 ⁇ m. Experience with the aforementioned developer materials reveals degradation of copy quafity as reflected by blurred and mottled prints having poor edge acuity and resolution.
- the invention as claimed is intended to provide developer materials which overcome the above noted deficiencies. This is achieved by the use of a developer mixture which is characterised in that the toner particles are of a size between a lower size limit of 3 ⁇ m and an upper size limit of 10. ⁇ m, particles of sizes smaller than the lower size limit and larger than the upper size limit having been removed, and in that the carrier particles have a size between 10 and 40 ⁇ m.
- the toner materials have a particle size in the range of between 3 ⁇ m and 10 ⁇ m and the carrier materials have a mean particle size in the range of between 10 ⁇ m and 40 ⁇ m.
- the invention offers the advantages of developer materials having more stable electrostatographic properties, improved triboelectric properties and a longer useful life. These developer materials are less susceptible to toner impaction, they are more resistant to film formation, i.e. the formation of a thin film of toner material, on electrostatographic recording surfaces, and enable the attainment of copied images having greatly improved quality.
- toner particles having a diameter below 3 ⁇ m usually encompass free colorant such as carbon black, and unpigmented platelets which are undesirable since they inhibit proper triboelectric charging and reduce the active carrier surface area resulting in high background deposition of such particles.
- toner particles having a diameter below 3 microns are triboelectrically charged too highly and they tend to not be developed as easily as the larger particles and also prevent the larger particles from being charged high enough. These lower charged larger particles are difficult to control in a developer mixture and will usually undesirably develop onto the background areas of an electrostatic latent image.
- the background deposit is not perceivable by the naked eye.
- the carrier particles due to the smaller size of the carrier particles employed in the developer mixtures of this invention, it is now possible for the carrier particles to carry sufficient toner particles to enable development of large solid areas without employing excessively high toner concentrations which previously led to unacceptably high image background deposits.
- the enhanced surface/volume ratio of the developer mass provides increased toner carrying capacity and consequently improved toner concentration latitude.
- the developer materials of this invention provide improved insulation between adjacent carrier beads when the carrier particles are made of a conductive metal and the carrier particles do not contain a coating of an insulating material. This is due to the increased population of toner particles between contacting carrier particles which improves the resistance to shorting between conductive carrier particles and the photoreceptor.
- the carrier material should preferably be conductive to realize the virtual electrode effect for maximum development and to prevent build-up of net electrical charge.
- the combination of developer materials of this invention has been found to provide prints of outstanding high quality which are indistinguishable from offset prints.
- the developer compositions of this invention provide developed images having a more uniform and lower pile height than achieved with conventional electrostatographic developer compositions.
- conventional developer compositions in a high speed electrostatographic copying/duplicating machine, such as the Xerox 9200
- the developed, unfused image toner pile height is between about 45 and 55 pm.
- 'Xerox' and '9200' are Registered Trade Marks.
- the developed, unfused image toner pile height is only about 18 pm.
- the image density is about 1.3 but the lower toner pile height obtained with the compositions of this invention is due to their greater covering power; that is, a greater number of toner particles are packed closer together, absorbing more reflected light, and therefore the perceived image density is the same in both cases yet the toner pile height is much less with these new developer materials.
- This finding is significant since there has conventionally been a substantial disparity in toner pile height between developed, unfused solid image areas and developed, unfused line image areas.
- the toner pile height of developed, unfused solid image areas and that of developed, unfused line image areas is substantially the same.
- any suitable particle classification method may be employed to obtain the toner materials of this invention.
- Typical particle classification methods include air classification, screening, cyclone separation, elutriation, centrifugal separation, and combinations thereof.
- the preferred method of obtaining the toner materials of this invention is by centrifugal air classification. In this method, air or some other gas flows inwards in a spiral path through a flat, cylindrical chamber. Particles contained in the air flow are exposed to two antagonistic forces, viz., to the inwardly directed tractive force of the air, and to the outwardly directed centrifugal force of the particle. For a definite size of particles, that is, the "cut size", both forces are in equilibrium.
- the "cut size" usually depends upon the gradient of the spiral, the peripheral component, and the absolute dimension of the classifying chamber. Adjustment of the cut size may be effected through variation of the two factors first mentioned, while the range of the cut size may be determined by the respective dimension of the classifying chamber.
- any suitable particle classification method may be employed to obtain the carrier materials of this invention.
- Typical particle classification methods include air classification, screening, cyclone separation, elutriation, centrifugal separation and combinations thereof.
- the preferred method of obtaining the carrier materials of this invention is by screening or sieving.
- Any suitable vinyl resin having a melting point of at least about 110°F may be employed in the toner compositions.
- the vinyl resin may be a homopolymer or a copolymer of two or more vinyl monomers.
- Typical monomeric units which may be employed to form vinyl polymers include: styrene, p-chloro-styrene, vinyl naphthalene; ethylenically unsaturated monoolefins such as ethylene, propylene, butylene, isobutylene and the like; vinyl halides such as vinyl chloride, vinyl bromide, vinyl fluoride; vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate and the like; esters of alphamethylene aliphatic monocarboxylic acids such as methyl acrylate, ethyl acrylate, n-butylacrylate, isobutyl acrylate, dodecyl acrylate, n-octy
- Toner resins containing relatively high percentages of a styrene resin are preferred.
- the presence of a styrene resin is preferred because a greater degree of image definition is generally achieved upon latent image development. Further, denser images are obtained when at least about 25 percent by weight, based on the total weight of resin in the toner, of a styrene resin is present in the toner.
- the styrene resin may be a homopolymer of styrene or styrene homologues or copolymers of styrene with other monomeric groups containing a single methylene group attached to a carbon atom by a double bond.
- typical monomeric materials which may be copolymerized with styrene by addition polymerization include: P-chlorostyrene, vinyl naphthalene, ethylenically unsaturated monoolefins such as ethylene, propylene, butylene, isobutylene and the like; vinyl esters such as vinyl chloride, vinyl bromide, vinyl fluoride, vinyl acetate, vinyl pro- p ionate, vinvl benzoate.
- esters of alpha-methylene aliphatic monocarboxylic acids such as methyl acrylate, ethyl acrylate, n-butylacrylate, isobutyl acrylate, dodecyl acrylate, n-octyl acrylate, 2-chloroethyl acrylate, phenyl acrylate, methyl-alpha- chloroacrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate and the like; acrylonitrile, methacrylonitrile, acrylamide, vinyl ethers such as vinyl methyl ether, vinyl isobutyl ether, vinyl ethyl ether, and the like; vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone, methyl isopropenyl ketone and the like; vinylidene halides such as vinylidene chloride, vinylidene chlorofluor
- the vinyl resins including styrene type resins, may also be blended with one or more other resins if desired.
- the added resin is preferably another vinyl resin because the resulting blend is characterized by especially good triboelectric stability and uniform resistance against physical degradation.
- the vinyl resins employed for blending with the styrene type or other vinyl resin may be prepared by the addition polymerization of any suitable vinyl monomer such as the vinyl monomers described above. Other resins may also be blended with the vinyl resins of this invention.
- Typical non-vinyl resins include: rosin modified phenol formaldehyde, resins, oil modified epoxy resins, polyurethane resins, cellulosic resins, polyether resins and mixtures thereof.
- the resin component of the toner contains styrene copolymerized with another unsaturated monomer or a blend of polystyrene and another resin
- a styrene component of at least about 25 percent by weight based on the total weight of the resin present in the toner is preferred because denser images are obtained and a greater degree of image definition is achieved with a given quantity of toner material.
- Any suitable pigment or dye may be employed as the colorant for the toner particles.
- Toner colorants are well-known and include, for example, carbon black, nigrosine dye, aniline blue, Calco Oil Blue, chrome yellow, ultramarine blue duPont Oil Red, Quinoline Yellow, methylene blue chloride, phthalocyanine blue, Malachite Green Oxalate, lamp black, Rose Bengal and mixtures thereof.
- the pigment or dye should be present in the toner in a quantity sufficient to render it highly coloured so that it will form a clearly visible image on a recording member.
- the toner may comprise a black pigment such as carbon black, for example, furnace black or channel black, or a black dye such as Amaplast Black dye, available from the National Aniline Products, Inc.
- a black pigment such as carbon black, for example, furnace black or channel black
- a black dye such as Amaplast Black dye, available from the National Aniline Products, Inc.
- the pigment is employed in an amount from about 1 percent to about 20 percent by weight based on the total weight of the coloured toner. If the toner colorant employed is a dye, substantially smaller quantities of colorant may be used.
- concentration preferably should be less than about 10 percent by weight of the colored toner.
- toner and developer materials include U.S. Patent 2,788,288, U.S. Patent 3,079,342, U.S. Reissue Patent 25,136, U.S. Patent 3,577,345, U.S. Patent 3,653,893, U.S. Patent 3,590,000, U.S. Patent 3,655,374, U.S. Patent 3,720,617, and U.S. Patent 3,819,367.
- Particular preferred for use in the present invention are those compositions disclosed in U.S. Reissue Patent 25,136 and U.S. Patent 3,079,342 containing a copolymer of styrene and alkyl methacrylate; the compositions disclosed in U.S.
- Patent 3,590,000 comprising a solid, stable hydrophilic metal salt of a fatty acid such as zinc stearate, and a polymeric esterification product of a dicarboxylic acid and a diol comprising a diphenol; and the compositions disclosed in U.S. Patent 3,819,367 containing a minor proportion of submicroscopic silicon dioxide additive particles.
- the toner compositions may be prepared by a well-known toner mixing and comminution technique.
- the ingredients may be thoroughly mixed by blending, mixing and milling the components and thereafter micro- pulverizing the resulting mixture.
- Another well-known technique for forming toner particles is to spray-dry a ball-milled toner composition comprising a colorant, a resin, and a solvent.
- any suitable coated or uncoated electrostatographic carrier bead material may be employed as the carrier material of this invention.
- Typical carriers include sodium chloride, ammonium chloride, aluminium potassium chloride. Rochelle salt, sodium nitrate, aluminium nitrate, potassium chlorate, granular zircon, granular silicon, methyl methacrylate, glass and silicon dioxide.
- Typical magnetic brush development process carriers include nickel, steel iron, ferrites, and the like, and are preferred in the compositions of this invention. The carriers may be employed with or without a coating. Many of the foregoing and other typical carriers are described by L. E. Walkup, et al in U.S. Pat. No. 2,638,416 and E. N. Wise in U.S. Pat. No.
- the carrier materials have semiconductive to conductive properties.
- the carrier materials of this invention may be coated with any suitable insulating material.
- Typical electrostatographic carrier particle coating materials include vinyl chloride-vinyl acetate copolymers, styrene- acrylate-organosilicon terpolymers, natural resins such as caoutchouc, colophony, copal, dammar, jalap, storax; thermoplastic resins including the polyolefins such as polyethylene, polypropylene, chlorinated polyethylene, and chlorosulfonated polyethylene; polyvinyls and polyvinylidenes such as polystyrene, poly- methylstyrene, polymethyl methacrylate, polyacrylonitrile, polyvinyl acetate, polyvinyl alcohol, polyvinyl butyral, polyvinyl chloride, polyvinyl carbazole, polyvinyl ethers, and polyvinyl ketones; fluor
- any suitable electrostatographic carrier coating thickness may be employed.
- a carrier coating having a thickness of at least sufficient to form a thin film on the carrier particle is preferred because the carrier coating will then possess sufficient thickness to resist abrasion and prevent pinholes which adversely affect the triboelectric properties of the coated carrier particles.
- the carrier coating may comprise from about 0.1 percent to about 10.0 percent by weight based on the weight of the coated carrier particles.
- the carrier coating should comprise from about 0.3 percent to about 1.5 percent by weight based on the weight of the coated carrier particles because maximum durability, toner impaction resistance, and copy quality are achieved.
- additives such as plasticizers, reactive and non-reactive polymers, dyes, pigments, wetting agents and mixtures thereof may be mixed with the coating materials and the coating may be continuous or discontinuous.
- the carrier coating composition may be applied to the carrier cores by any conventional method such as spraying, dipping, fluidized bed coating, tumbling, brushing, and the like.
- the coating compositions may be applied as a powder, a dispersion, solution, emulsion or hot melt.
- any suitable solvent may be employed. Solvents having relatively low boiling points are preferred because less energy and time is required to remove the solvent subsequent to application of the coating to the carrier cores.
- the coating may comprise resin monomers which are polymerized in situ on the surface of the cores or plastisols gelled in situ to a non-flowable state on the surface of the cores.
- any suitable organic or inorganic photoconductive material may be employed as the recording surface with the developer materials of this invention.
- Typical inorganic photoconductor materials include: sulfur, selenium, zinc sulfide, zinc oxide, zinc cadmium sulfide, zinc magnesium oxide, cadmium selenide, zinc silicate, calcium strontium sulfide, cadmium sulfide, mercuric iodide, mercuric oxide, mercuric sulfide, indium trisulfide, gallium selenide, arsenic disulfide, arsenic trisulfide, arsenic triselenide, antimony trisulfide, cadmium sulfoselenide and mixtures thereof.
- Typical organic photoconductors include: quinacridone pigments, phthalocyanine pigments, triphenylamine, 2,4 - bis(4,4' - diethylamino- phenol) - 1, 3,4 - oxadiazol, N - isopropyl- carbazole, triphenylpyrrole, 4,5 - diphenyl- imidazolidinone, 4,5 - diphenyl - imidazolidine- thione, 4,5 - bis(4' - amino - phenyl) - imidazoli- dinoile, 1,5 - dicyanonaphthalene, 1,4 - dicyanonaphthalene, aminophthalodinitrile, nitrophthalodinitrile, 1,2,5,6 - tetraazacyclo- octatetracene - 2,4,6,8), 2 - mercaptobenzothiazole - 2 - phenyl - 4 - bisphenylideneoxa-
- photoconductive materials include U.S. Pat. No. 2,803,542 to Ullrich, U.S. Pat. No. 2,970,906 to Bixby, U.S. Pat. No. 3,121,006 to Middleton, and U.S. Pat. No. 3,151,982 to Corrsin.
- a control developer mixture is prepared by mixing a toner composition comprising a mixture of 90 parts by weight of a copolymer of 58.0 percent by weight of styrene and 42.0 percent by weight of n-butyl methacrylate, and 10 parts by weight of a furnace carbon black with carrier particles.
- the toner particles were determined to have a particle size of between 8 and 30,um.
- the carrier particles comprised 100 ⁇ m nickel-zinc ferrite coated with 0.6 percent by weight, based on the weight of the core material, of a carrier coating composition comprising styrene, a methacrylate ester, and an organosilicon compound as disclosed in U.S. Pat. No. 3,526,533.
- the coated ferrite carrier material was determined to have a specific surface area of about 151 cm 2 /gram.
- toner particles About 1 part by weight of the toner particles was mixed with about 100 parts by weight of the carrier particles to form the developer mixture. Copies of a standard test pattern were made with the developer mixture in an electrostatographic copying machine employing a magnetic brush development system. It was found that the developer mixture failed after about 300,000 copies. Developer failure was experienced in the form of high background, i.e., exceeding the specified 0.01 background density level at 1.0 solid area density. A high level of photoreceptor filming, i.e. disposition of a thin film of toner material on the photoreceptor, was observed as print-out on the copies which occurred at a frequency of about every 60,000 intervals. The rate of toner impaction was found to be about 8 mg/g. The copies produced were found to have blurred images, with poor edge acuity. Grey scale and half-tone reproduction quality was poor. Copy resolution was less than 7 line pairs per millimetre and the presence of hollow characters was substantial.
- a developer mixture was prepared by mixing about 3 parts of the toner material employed in Example I with about 100 parts of carrier material except that the toner particles were selected to have a particle size of between 3 and 10 ⁇ m.
- the carrier particles were selected to comprise 35 micron nickel powder.
- the nickel powder was determined to have a specific surface area of about 450 cm 2 /gram.
- the developer mixture was used to develop an electrostatic latent image under substantially the same conditions as in Example I. It was found that the developer mixture performed satisfactorily up to about 300,000 copies after which the test was suspended. No photoreceptor filming was observed as print-out on the copies. The rate of toner impaction was insignificant and not measurable using existing techniques.
- the copies produced contained images free of blur and edge acuity was excellent. Grey scale and half-tone reproduction quality was excellent. Copy resolution was about 10 line pairs per millimetre and no hollow characters were evident.
- a developer mixture was prepared by mixing about 3 parts by weight of a toner composition comprising a mixture of 88.5 parts by weight of a polymeric esterification product of a dicarboxylic acid and a diol comprising a diphenol, and 11.5 parts by weight of a carbon black as disclosed in U.S. Patent 3,590,000 with about 100 parts by weight of carrier particles.
- the toner particles were selected to have a particle size of between 3 and 10 ,um.
- the carrier particles comprised 35 ,um nickel powder. By calculation, the nickel powder was determined to have a specific surface area of about 450 cm 2 /gram.
- the developer mixture was used to develop an electrostatic latent image under substantially the same conditions as in Example I. It was found that the developer mixture performed satisfactorily up to about 300,000 copies after which the test was suspended. No photoreceptor filming was observed as print-out on the copies. The rate of toner impaction was insignificant and not measurable using existing techniques.
- the copies produced contained images free of blur and edge acuity was excellent. Grey scale and half-tone reproduction quality was excellent. Copy resolution was about 10 line pairs per millimetre and no hollow characters were evident.
- a developer mixture was prepared by mixing about 3 parts of the toner material employed in Example III with about 100 parts of the carrier material employed in Example III except that 0.65 parts by weight of submicroscopic silicon dioxide particles (Aerosil (Registered Trade Mark) R-972) based on the weight of the toner particles as described in U.S. Patent 3,819,367 was added to the developer mixture.
- submicroscopic silicon dioxide particles Aerosil (Registered Trade Mark) R-972
- the developer mixture was used to develop an electrostatic latent image under substantially the same conditions as in Example I. It was found that the developer mixture performed satisfactorily up to about 300,000 copies after which the test was suspended. No photoreceptor filming was observed as print-out on the copies. The rate of toner impaction was excellent and not measurable using existing techniques.
- the copies produced contained images free of blur and edge acuity was excellent. Grey scale and half-tone reproduction quality was excellent. Copy resolution was about 10 line pairs per millimetre and no hollow characters were evident.
- a developer mixture was prepared as in Example IV except that 0.35 parts by weight of zinc stearate based on the weight of the toner particles as described in U.S. Patent 3,590,000 was added to the developer mixture.
- the developer mixture was used to develop an electrostatic latent image under substantially the same conditions as in Example I. It was found that the developer mixture performed satisfactorily up to about 300,000 copies after which the test was suspended. No photoreceptor filming was observed as print-out on the copies. The rate of toner impaction was insignificant and was not measurable using existing techniques.
- the copies produced contained images free of blur and edge acuity was excellent. Grey scale and half-tone reproduction quality was excellent. Copy resolution was about 10 line pairs per millimetre and no hollow characters were evident.
- a developer mixture was prepared by mixing about 3 parts by weight of a toner composition comprising a mixture of 80 parts by weight of styrene, 20 parts by weight of isobutyl methacrylate, and 10 parts by weight of a carbon black with about 100 parts by weight of carrier particles.
- the toner particles were determined to have a particle size of between 3 and 1O ⁇ m.
- the carrier particles comprised 35 ⁇ m nickel powder.
- the developer mixture was used to develop an electrostatic latent image under substantially the same conditions as in Example I. It was found that the developer mixture performed satisfactorily up to about 300,000 copies after which the test was suspended. No photoreceptor filming was observed as print-out on the copies. The rate of toner impaction was insignificant and not measurable using existing techniques.
- the copies produced contained images free of blur and edge acuity was excellent. Grey scale and half-tone reproduction quality was excellent. Copy resolution was about 10 line pairs per millimetre and no hollow characters were evident.
- a developer mixture was prepared by mixing about 3 parts by weight of a toner composition comprising a mixture of 80 parts by weight of styrene, 20 parts by weight of isobutyl methacrylate, 15 parts by weight of diphenyl isophthalate, and 10 parts by weight of a carbon black with about 100 parts by weight of carrier particles.
- the toner particles were determined to have a particle size of between 3 and 10 pm.
- the carrier particles comprised 35 ,um nickel powder.
- the developer mixture was used to develop an electrostatic latent image under substantially the same conditions as in Example I. It was found that the developer mixture performed satisfactorily up to about 300,000 copies after which the test was suspended. No photoreceptor filming was observed as print-out on the copies. The rate of toner impaction was insignificant and not measurable using existing techniques.
- the copies produced contained images free of blur and edge acuity was excellent. Grey scale and half-tone reproduction quality was excellent. Copy resolution was about 10 line pairs per millimetre and no hollow characters were evident.
- the developer materials of this invention are characterized as providing substantially improved copy quality in the development of electrostatic latent images. It is believed that developed image resolution is improved due to the toner particle size range. The improved edge acuity is believed to result from less edge raking by the smaller carrier particles in the present developer mixtures. The reduced mottle appearance and absence of hollow characters of copied images obtained appears to result from more uniform latent image development and image transfer due to more uniform triboelectric charge of the developer materials. Improved grey scale and half-tone reproduction obtained with the developer materials of this invention appears to be due to the high developability of these smaller toner particles and the virtual electrode effect at the photoreceptor surface of the smaller conductive carrier particles.
- developer materials of this invention are further characterized as resulting in improved machine performance with longer systems life, that is, these developer materials provide substantially improved triboelectric charging properties of the developer mixtures'for substantially longer periods of time thereby increasing the developer life of the developer mixtures and decreasing the time intervals between replacement of the developer materials.
- the developer materials of this invention may be characterized as providing dense images and are particularly useful in magnetic brush development systems.
- the developer materials of this invention may be further characterized as experiencing substantially reduced impaction rates resulting in more stable triboelectric charging properties of the developer mixtures for substantially longer periods of time thereby increasing the developer life of the developer mixtures and decreasing the time intervals between replacement of the developer materials.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US89391578A | 1978-04-06 | 1978-04-06 | |
US893915 | 1978-04-06 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0004748A2 EP0004748A2 (en) | 1979-10-17 |
EP0004748A3 EP0004748A3 (en) | 1979-11-14 |
EP0004748B1 true EP0004748B1 (en) | 1984-03-14 |
Family
ID=25402330
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP79300512A Expired EP0004748B1 (en) | 1978-04-06 | 1979-03-29 | Electrostatographic developer mixture and imaging process |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0004748B1 (enrdf_load_stackoverflow) |
JP (1) | JPS54134636A (enrdf_load_stackoverflow) |
BR (1) | BR7901932A (enrdf_load_stackoverflow) |
CA (1) | CA1147192A (enrdf_load_stackoverflow) |
DE (1) | DE2966772D1 (enrdf_load_stackoverflow) |
MX (1) | MX153082A (enrdf_load_stackoverflow) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5796353A (en) * | 1980-12-06 | 1982-06-15 | Mita Ind Co Ltd | Two component system developer for magnetic brush development |
JPS5926943B2 (ja) * | 1980-12-30 | 1984-07-02 | コニカ株式会社 | 静電荷像現像用トナ− |
JPH079543B2 (ja) * | 1983-05-26 | 1995-02-01 | キヤノン株式会社 | 静電荷像現像用トナ− |
JPH079544B2 (ja) * | 1983-07-29 | 1995-02-01 | キヤノン株式会社 | トナ− |
JPH083659B2 (ja) * | 1986-05-16 | 1996-01-17 | キヤノン株式会社 | 静電荷像現像用トナー及び現像方法 |
JP2787305B2 (ja) * | 1986-09-29 | 1998-08-13 | 株式会社リコー | 電子写真現像方法 |
JP2661091B2 (ja) * | 1988-01-20 | 1997-10-08 | ミノルタ株式会社 | 現像剤 |
JPH0776847B2 (ja) * | 1990-11-30 | 1995-08-16 | 富士ゼロックス株式会社 | スライド作製用カラートナー |
JP2985594B2 (ja) * | 1992-12-03 | 1999-12-06 | セイコーエプソン株式会社 | 画像形成方法 |
EP0656130B1 (en) * | 1993-06-22 | 1996-01-31 | Agfa-Gevaert N.V. | Electrostatographic developer composition |
JPH10221880A (ja) * | 1997-02-07 | 1998-08-21 | Toshiba Corp | 電子写真用現像剤及びこれを用いた現像装置 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE626060A (enrdf_load_stackoverflow) * | 1961-12-16 | |||
US3547822A (en) * | 1968-02-01 | 1970-12-15 | Eastman Kodak Co | Scum-retardant carrier particles and compositions thereof |
US3781207A (en) * | 1968-12-18 | 1973-12-25 | Continental Can Co | Developer mixture for electrostatic printing |
CA944106A (en) * | 1970-01-12 | 1974-03-26 | Reprographic Materials | Agglomeration of pigment particles and compositions utilizing same |
GB1279231A (en) * | 1970-04-09 | 1972-06-28 | Sperry Rand Corp | Electrostatographic developer |
GB1391661A (en) * | 1972-02-20 | 1975-04-23 | Oce Van Der Grinten Nv | Toner powder and its use in electrophotographic copying processes |
CA1041344A (en) * | 1974-05-30 | 1978-10-31 | Lewis O. Jones | High surface area carrier |
CA1043149A (en) * | 1974-05-30 | 1978-11-28 | Lewis O. Jones | Classified toner materials, developer mixture and imaging system |
CA1132827A (en) * | 1977-11-03 | 1982-10-05 | Jerry J. Abbott | Electrophotographic toner comprising particles of a specific size distribution |
-
1979
- 1979-02-28 CA CA000322602A patent/CA1147192A/en not_active Expired
- 1979-03-29 EP EP79300512A patent/EP0004748B1/en not_active Expired
- 1979-03-29 BR BR7901932A patent/BR7901932A/pt unknown
- 1979-03-29 DE DE7979300512T patent/DE2966772D1/de not_active Expired
- 1979-03-30 JP JP3828079A patent/JPS54134636A/ja active Granted
- 1979-04-03 MX MX177185A patent/MX153082A/es unknown
Also Published As
Publication number | Publication date |
---|---|
JPS6360381B2 (enrdf_load_stackoverflow) | 1988-11-24 |
CA1147192A (en) | 1983-05-31 |
DE2966772D1 (en) | 1984-04-19 |
EP0004748A2 (en) | 1979-10-17 |
MX153082A (es) | 1986-07-30 |
BR7901932A (pt) | 1979-11-27 |
EP0004748A3 (en) | 1979-11-14 |
JPS54134636A (en) | 1979-10-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1043149A (en) | Classified toner materials, developer mixture and imaging system | |
EP0022347B1 (en) | Electrostatographic developer mixture | |
CA1121201A (en) | Electrostatographic toner composition containing a highly fluorinated surface active additive providing positive triboelectric charging potential | |
US5683844A (en) | Fibrillated carrier compositions and processes for making and using | |
US4233387A (en) | Electrophotographic carrier powder coated by resin dry-mixing process | |
US3969251A (en) | Developer mixture | |
US4040969A (en) | High surface area carrier | |
CA1041344A (en) | High surface area carrier | |
US3942979A (en) | Imaging system | |
US3893934A (en) | Solid developer for electrostatic latent images | |
EP0004748B1 (en) | Electrostatographic developer mixture and imaging process | |
US4391890A (en) | Developer compositions containing alkyl pyridinium toluene sulfonates | |
US6143456A (en) | Environmentally friendly ferrite carrier core, and developer containing same | |
US4078930A (en) | Developer compositions comprising toner and carrier | |
US4122024A (en) | Classified toner materials | |
CS212772B2 (en) | Electrostaographic material for developing electrostatic latent images | |
US4198477A (en) | Method of using electrostatographic toner composition with surfactant | |
US4002776A (en) | Imaging process employing toner particles containing arylsulphonamide formaldehyde adduct | |
US4304830A (en) | Toner additives | |
US4324851A (en) | Positive color toners | |
US4179388A (en) | Electrostatographic developer with smooth surfaced carrier | |
US4126454A (en) | Imaging process utilizing classified high surface area carrier materials | |
US4859558A (en) | Composition with fatty acid bisamide powder developer | |
US4053310A (en) | Durable carrier coating compositions comprising polysulfone | |
EP0479875B1 (en) | Dry electrostatographic toner composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Designated state(s): DE GB NL |
|
AK | Designated contracting states |
Designated state(s): DE GB NL |
|
17P | Request for examination filed | ||
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Designated state(s): DE GB NL |
|
REF | Corresponds to: |
Ref document number: 2966772 Country of ref document: DE Date of ref document: 19840419 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19870331 Year of fee payment: 9 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19890329 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19891001 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee | ||
GBPC | Gb: european patent ceased through non-payment of renewal fee | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19960328 Year of fee payment: 18 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19971202 |