EP0020181A1 - Process for preparing coated carrier particles for electrostatographic developers - Google Patents
Process for preparing coated carrier particles for electrostatographic developers Download PDFInfo
- Publication number
- EP0020181A1 EP0020181A1 EP80301870A EP80301870A EP0020181A1 EP 0020181 A1 EP0020181 A1 EP 0020181A1 EP 80301870 A EP80301870 A EP 80301870A EP 80301870 A EP80301870 A EP 80301870A EP 0020181 A1 EP0020181 A1 EP 0020181A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- particles
- carrier
- powdered
- mixture
- preparing
- 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.)
- Withdrawn
Links
- 239000002245 particle Substances 0.000 title claims abstract description 179
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000000203 mixture Substances 0.000 claims abstract description 98
- 239000012530 fluid Substances 0.000 claims abstract description 27
- 239000007787 solid Substances 0.000 claims abstract description 20
- 239000012260 resinous material Substances 0.000 claims abstract description 14
- 239000006258 conductive agent Substances 0.000 claims abstract description 10
- 238000004220 aggregation Methods 0.000 claims abstract description 4
- 230000002776 aggregation Effects 0.000 claims abstract description 4
- 239000012876 carrier material Substances 0.000 claims description 34
- 238000000576 coating method Methods 0.000 claims description 33
- 239000011248 coating agent Substances 0.000 claims description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 28
- 229910052742 iron Inorganic materials 0.000 claims description 14
- 239000002033 PVDF binder Substances 0.000 claims description 10
- 238000010438 heat treatment Methods 0.000 claims description 10
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims description 10
- 229910000831 Steel Inorganic materials 0.000 claims description 8
- 239000010959 steel Substances 0.000 claims description 8
- -1 ethylenepropylene, trichlorofluorethylene Chemical class 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 239000004800 polyvinyl chloride Substances 0.000 claims description 6
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 6
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- 239000007771 core particle Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000004812 Fluorinated ethylene propylene Substances 0.000 claims description 3
- 229920009441 perflouroethylene propylene Polymers 0.000 claims description 3
- 229920001774 Perfluoroether Polymers 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 238000007580 dry-mixing Methods 0.000 claims description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 229910002804 graphite Inorganic materials 0.000 claims description 2
- 239000010439 graphite Substances 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- 239000002923 metal particle Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 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 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 2
- 238000012546 transfer Methods 0.000 claims description 2
- 229910000859 α-Fe Inorganic materials 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 229910001507 metal halide Inorganic materials 0.000 claims 1
- 229910052976 metal sulfide Inorganic materials 0.000 claims 1
- 238000011161 development Methods 0.000 abstract description 14
- 239000008247 solid mixture Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 description 56
- 239000011162 core material Substances 0.000 description 50
- 238000000034 method Methods 0.000 description 25
- 239000004020 conductor Substances 0.000 description 16
- 239000008199 coating composition Substances 0.000 description 14
- 239000000843 powder Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 239000006229 carbon black Substances 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- 238000000227 grinding Methods 0.000 description 8
- 108091008695 photoreceptors Proteins 0.000 description 8
- 239000011342 resin composition Substances 0.000 description 8
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 229920006370 Kynar Polymers 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 229920001169 thermoplastic Polymers 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- 239000000969 carrier Substances 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229920001897 terpolymer Polymers 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000003801 milling Methods 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000003570 air Substances 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- LFMIQNJMJJKICW-UHFFFAOYSA-N 1,1,2-trichloro-2-fluoroethene Chemical group FC(Cl)=C(Cl)Cl LFMIQNJMJJKICW-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
- 240000000972 Agathis dammara Species 0.000 description 1
- 241001561902 Chaetodon citrinellus Species 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 239000004859 Copal Substances 0.000 description 1
- 235000010919 Copernicia prunifera Nutrition 0.000 description 1
- 244000180278 Copernicia prunifera Species 0.000 description 1
- 229920002871 Dammar gum Polymers 0.000 description 1
- 241000782205 Guibourtia conjugata Species 0.000 description 1
- 240000007597 Hymenaea verrucosa 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
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004952 Polyamide 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
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-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
- 241001060310 Styracaceae Species 0.000 description 1
- 235000001361 Styrax officinalis Nutrition 0.000 description 1
- 241000736873 Tetraclinis articulata Species 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 229920006387 Vinylite Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 239000010426 asphalt Substances 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
- 239000011324 bead Substances 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
- 230000002902 bimodal effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000012050 conventional carrier Substances 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
- 230000007812 deficiency Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000001914 filtration Methods 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
- 238000004108 freeze drying Methods 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
- 230000004927 fusion Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000009689 gas atomisation Methods 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 229920000554 ionomer Polymers 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
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229940002712 malachite green oxalate Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000002739 metals Chemical class 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
- 239000000178 monomer Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) 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
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920013716 polyethylene resin 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
- 229920000642 polymer 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
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005990 polystyrene resin 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
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol 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
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 229940051201 quinoline yellow Drugs 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
- 239000004172 quinoline yellow Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000009692 water atomization Methods 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
- 230000004580 weight loss Effects 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 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
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1131—Coating methods; Structure of coatings
-
- 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
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1132—Macromolecular components of coatings
- G03G9/1133—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/1134—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds containing fluorine atoms
-
- 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
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1138—Non-macromolecular organic components of coatings
-
- 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
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1139—Inorganic components of coatings
Definitions
- This invention relates to a process for preparing coated carrier particles for electrostatographic developers.
- the resulting electrostatic latent image is developed by depositing thereon a finely-divided electroscopic material referred to in the art as toner, the toner being generally attracted to the areas of the layer which retain a charge thus forming a toner image corresponding to the electrostatic latent image. Subsequently, the toner image can be transferred to a support surface such as paper and this transferred image can be permanently affixed to the support surface using a variety of techniques including pressure fixing, heat fixing, solvent fixing, and the like.
- Carrier materials used in the development of electrostatic latent images are described in many patents including, for example, U.S. Patent 3,590,000.
- the type of carrier material to be used depends on many factors such as the type of development used, the quality of the development desired, the type of photoconductive material employed and the like.
- the materials used as carrier surfaces or carrier particles or the coating thereon should have a triboelectric value commensurate with the triboelectric value of the toner in order to generate electrostatic adhesion of the toner to the carrier.
- Carriers should be selected that are not brittle so as to cause flaking of the surface or particle break-up under the forces exerted on the carrier during recycle as such causes undesirable effects and could, for example, be transferred to the copy surface thereby reducing the quality of the final image.
- the coating materials employed for carrier particles are generally resins having electrically insulating properties and are usually applied by solution or spray-drying techniques.
- the coating materials employed for carrier particles are generally resins having electrically insulating properties and are usually applied by solution or spray-drying techniques.
- Attempts to resolve this problem by increasing carrier coating weights, for example, to as much as up to about 3 percent or greater to provide an effective triboelectric charging coating to the carrier particles necessarily involves handling excessive quantities of solvents and usually results in low product yields.
- toner impaction i.e., where toner particles become welded to or impacted upon the carrier particles, remains high with thus coated carrier particles producing short developer useful lifetimes.
- solution-coated porous carrier particles when combined and mixed with finely-divided toner particles provide triboelectric charging levels which are too low for practical use.
- solution-coated metallic carrier particles have a high incidence of electrical breakdown at low applied voltages leading to shorting between the carrier particles and the photoreceptor.
- an electrostatic carrier and toner powder combination in order to develop a latent image comprised of negative electrostatic charges, an electrostatic carrier and toner powder combination must be selected in which the toner is triboelectrically charged positively relative to the granular carrier.
- an electroscopic toner powder and carrier mixture in order to develop a latent image comprised of positive electrostatic charges such as where a selenium photoreceptor is employed, an electroscopic toner powder and carrier mixture must be selected in which the toner is triboelectrically charged negatively relative to the carrier.
- the latent image is formed of negative electrostatic charges such as when employing an organic electrophotosensitive material as the photoreceptor, it is highly desirable to develop the latent image with a positively charged electroscopic powder and a negatively charged carrier material.
- the present invention is intended to provide a carrier manufacturing technique which results in a product that overcomes the above-noted deficiencies of conventional developer materials.
- the process of the invention is characterised by preparing a fluid mixture of insulating resinous material and at least one electrically conductive agent, converting said fluid mixture to a solid state, comminuting said mixture in said solid state to dry, powdered particles, applying said powdered particles to the surface of carrier cores, and heating the resultant aggregation so that said powdered particles fuse to said carrier cores.
- the resultant carrier beads have conductive characteristics, greatly increased useful life, and substantially eliminate photoreceptor shorting problems.
- the triboelectric values of a carrier material are altered without markedly changing the physical and chemical properties of the original carrier material.
- the improved developer materials may be used in electrostatographic development environments where the photoreceptor is negatively charged.
- the carrier particles of this invention comprise a core particle having an average diameter of between 30 and 1,000 microns coated with between 0.05 and 3.0 percent by weight, based on the weight of the coated carrier particles, of a mixture of thermoplastic insulating resinous material and at least one agent possessing electrically conductive properties.
- the coated carrier particles of this invention are provided by preparing a fluid mixture of thermoplastic insulating resinous material and at least one electrically conductive agent, applying said mixture in the form of dry, powdered particles having a particle size of between 1 and 100 microns to the aforementioned carrier core, and then heating the resultant aggregation to a temperature of between 12 6°C and 345 0 C for between 15 and 120 minutes so that the mixture of thermoplastic insulating resinous material and electrically conductive agent fuse to the carrier core particle.
- any suitable means may be employed to produce the conductive material- powdered resin mixture.
- an insulating resinous material is heat-melted or dissolved in a suitable solvent to bring the resinous material to a fluid or tacky state.
- a suitable amount of conductive material is then processed to provide dry, powdered particles having a particle size of between about 1 micron and about 100 microns, preferably between I micron and about 50 microns.
- Some of the means which may be employed to provide these dry, powdered resin-conductive material particles include spray-drying the foregoing fluid or tacky mixture or a dispersion thereof, precipitation of a resin-conductive material dispersion, freeze-drying a resin-conductive material dispersion, air or fluid attrition of a resin-conductive material dispersion, direct polymerization such as emulsion polymerization of conductive material in a monomer followed by crushing, grinding, or milling and any other suitable means to obtain the aforedescribed particles.
- the powdered particles are applied to the surface of a carrier core material by, for example, dry-mixing the powdered resin-conductive material particles and the carrier core material until the powdered particles adhere to the carrier core material by mechanical impaction and/or electrostatic attraction.
- Any suitable means may be employed for this purpose.
- Typical means for this purpose include combining the carrier core material and the powdered particles mixture by cascade roll-milling or tumbling, mulling, shaking, electrostatic powder cloud spraying, employing a fluidized bed, electrostatic disc processing, and an electrostatic curtain.
- the mixture of carrier material and powdered particles is heated to permit flow-out of the coating material powder particles over the surface of the carrier core material.
- the coated carrier particles are cooled and classified to the desired particle size.
- the resultant coated carrier particles may have a fused coating over between about 15 percent and up to about 85 percent of their surface area.
- the concentration of coating material powder particles as well as the conditions of the heating step may be selected as to form a continuous film of the coating material on the surface of the carrier core material or leave selected areas of it uncoated. Where selected areas of the carrier core material remain uncoated or exposed, the carrier material will possess more strongly electrically conductive properties when the core material comprises a metal.
- these carrier materials may possess both electrically insulating and electrically conductive properties. Due to the electrically conductive properties of these carrier materials, the carrier materials provide desirably high triboelectric charging values when mixed with finely-divided toner particles.
- the dry, powdered resin-conductive material compositions and coating technique of this invention have been found to be especially effective in coating porous carrier cores to obtain coated carrier particles capable of generating high and useful triboelectric charging values to finely-divided toner particles and carrier particles and which possess significantly increased resistivities.
- carrier particles are prepared by the powder coating technique of this invention, the majority of the coating material particles are fused to the carrier surface and thereby reduce the number of potential toner impaction sites on the carrier material.
- any suitable solid material having an average particle diameter of between about 30 microns and about 1,000 microns may be employed as the carrier core in this invention.
- the carrier core material be selected so that the coated core material acquire a charge having a polarity opposite to that of the toner particles when brought into close contact therewith so that the toner particles adhere to and surround the carrier particles.
- the carrier particles be selected so that the toner particles acquire a positive charge and the carrier particles acquire a negative triboelectric charge.
- the polarities of their charge when mixed are such that the electroscopic toner particles adhere to the surface of the carrier particles and also adhere to that portion of the electrostatic image-bearing surface having a greater attraction for the toner particles than the carrier particles.
- the carrier core material comprise low density, porous, magnetic or magnetically-attractable metal particles having a gritty, oxidized surface and a high surface area, i.e., a surface area which is at least about 200 cm2/gram and up to about 1300 cmYgram of carrier material.
- Typical satisfactory carrier core materials include iron, steel, ferrite, magnetite, nickel and mixtures thereof.
- the carrier core materials For ultimate use in an electrostatographic magnetic brush development system, it is preferred that the carrier core materials have an average particle size of between about 30 microns and about 250 microns. Excellent results have been obtained when the carrier core materials comprise porous, sponge iron or steel grit.
- the carrier core materials are generally produced by gas or water atomization processes or by reduction of suitable sized ore to yield sponge powder particles.
- the powders produced have a gritty surface, are porous, and have high surface areas.
- conventional carrier core materials usually have a high density and smooth surface characteristics.
- thermoplastic insulating resinous material which can be rendered in powdered form may be employed in this invention.
- Typical insulating coating materials include vinyl chloride-vinyl acetate copolymers, styrene-acrylate-organosilicon terpolymers, natural resins such as caoutchouc, carnauba, colophony, copal, dammar, jalap, storax; thermoplastic resins including the polyolefins such as chlorinated polyethylene, chlorosulfonated polyethylene, and copolymers and mixtures thereof; polyvinyls and polyvinyl- idenes such as polymethyl-styrene, polymethyl methacrylate, polyacrylonitrile, polyvinyl acetate, polyvinyl alcohol, polyvinyl butyral, polyvinyl chloride, polyvinyl pyridine, polyvinyl carbazole, polyvinyl ethers, and polyvinyl ketones; fluorocarbons such as polytetraflu
- the preferred powdered coating materials of this invention are selected from fluorinated ethylene, fluorinated propylene and copolymers, mixtures, combinations or derivatives thereof such as fluorinated ethylene-propylene commercially available from E.I.
- FEP trichloro- fluoroethylene, perfluoroalkoxy tetrafluoroethylene, polyvinylidene fluoride and the zinc and sodium salts of ionomer resins such as those containing carboxyl groups which are ionically bonded by partial neutralization with strong bases such as sodium hydroxide and zinc hydroxide to create ionic crosslinks in the intermolecular structure thereof and the like.
- polyethylene, polypropylene, styrene and styrene copolymers or terpolymers epoxy resins, polycarbonates, polysulfones, polyphenylene oxide, silicones, vinyl chloride and vinyl chloride copolymers, halogenated resins including homopolymers, copolymers, and terpolymers thereof.
- the resinous coating material be of the type capable of providing negative triboelectric charging values to the carrier particles wherein the toner particles obtain a positive triboelectric charge for attraction of the toner particles to a negatively charged photoconductive surface.
- any suitable organic or inorganic electrically conductive material may be employed in this invention.
- Typical electrically conductive materials include metals, metal oxides, sulfides, halides, carbon, graphite, phthalocyanines, charge transfer complexes, quaternary ammonium compounds, and other conductive materials such as those described in U.S. Patent No. 3,533,835.
- Any suitable concentration of conductive material in the carrier coating may be employed. Typically, a loading of between about 3% to about 75% by weight, based on the weight of the carrier coating composition, i.e. the powdered particles, provides adequate electrical conductivity to the carrier particles.
- Coating compositions having a volume resistivity of less than about 10 10 ohm-cm at 23° C are considered conductive.
- any suitable finely-divided toner material may be employed with the carrier materials of this invention.
- Typical toner materials include, for example, gum copal, gum sandarac, rosin, asphaltum, phenol-formaldehyde resins, rosin-modified phenol-formaldehyde resins, methacrylate resins, polystyrene resins, polystyrene-butadiene resins, polyester resins, polyethylene resins, epoxy resins and copolymers and mixtures thereof.
- the particular type of toner material to be used depends to some extent upon the separation of the toner particles from the coated carrier particles in the triboelectric series.
- Patents describing typical electroscopic toner compositions include U.S.
- the toner materials have an average particle diameter of between about 5 and 15 microns.
- Preferred toner resins include those containing a high content of styrene because they generate high triboelectric charging values and a greater degree of image definition is achieved when employed with the carrier materials of this invention. Generally speaking, satisfactory results are obtained when about 1 part by weight toner is used with about 10 to 200 parts by weight of conductive powder coated carrier 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, iron oxide, Rose Bengal and mixtures thereof.
- the pigment and/or dye should be present in the toner in a quantity sufficient to render it highly colored so that it will form a clearly visible image on a recording member.
- the toner may comprise a black pigment such as carbon black or a black dye such as Amaplast Black dye, available from National Aniline Products, Inc..
- the pigment is employed in an amount from about 3 percent to about 20 percent by weight, based on the total weight of the colored toner. If the toner colorant employed is a dye, substantially smaller quantities of colorant may be used.
- the developer compositions of the instant invention may be employed to develop electrostatic latent images on any suitable electrostatic latent image-bearing surface including conventional photoconductive surfaces.
- Well known photoconductive materials include vitreous selenium, organic or inorganic photoconductors embedded in a non-photoconductive matrix, organic or inorganic photoconductors embedded in a photoconductive matrix, or the like.
- Representative patents in which photoconductive materials are disclosed include U.S. Patent No. 2,803,542 to Ullrich; U.S. Patent No. 2,970,906 to Bixby; U.S. Patent No. 3,121,006 to Middleton; U.S. Patent No. 3,121,007 to Middleton; and U.S. Patent No. 3,151,982 to Corrsin.
- the relative triboelectric values generated by contact of carrier particles with toner particles is measured by means of a Faraday Cage.
- the device comprises a steel cylinder having a diameter of about 25 mm and a length of about 25 mm.
- a 400-mesh screen is positioned at each end of the cylinder.
- the cylinder is weighed, charged with about 0.5 gram mixture of carrier and toner particles and connected to ground through a capacitor and an electrometer connected in parallel. Dry compressed air is then blown through the steel cylinder to drive all the toner from the carrier.
- the charge on the capacitor is then read on the electrometer.
- the chamber is reweighed to determine the weight loss.
- the resulting data is used to calculate the toner concentration and the charge in microcoulombs per gram of toner. Since the triboelectric measurements are relative, the measurements should, for comparative purposes, be conducted under substantially identical conditions.
- a control carrier material is prepared comprising about 97 parts of sponge iron carrier cores (available from Hoeganaes Corporation, Riverton, New Jersey, under the tradename ANCOR EH 80/150) having an average particle diameter of about 150 microns.
- a coating composition comprising about 10 percent solids of polyvinyl chloride and trifluorochloroethylene prepared from a material commercially available as FPC 461 from Firestone Plastics Company, Pottstown, PA., dissolved in methyl ethyl ketone is applied to the carrier cores as to provide them with a coating weight of about 3 percent.
- the coating composition is applied to the carrier cores via solution coating employing a vibratub (available from Vibraslide, Inc., Binghamton, New York).
- the composition of the toner particles comprises about 87 parts of a 65/35 styrene-n-butyl methacrylate copolymer, about 10 parts of carbon black and about 3 parts of nigrosine SSB.
- the mixture of carrier particles and toner particles is employed in a magnetic brush development testing fixture equipped with a photoreceptor charged to a negative polarity. The testing fixture is set as to provide a solid area density of about 1.3 to developed electrostatic latent images.
- this developer mixture is unsatisfactory in that the triboelectric charge generated on the toner material is about 14 microcoulombs per gram of toner, and the image background density is about 0.04 which is considerably above the acceptable level of 0.01.
- the electrical resistivity of the developer is about 3.8 x 10 ohm-cms.
- a carrier material comprising about 99 parts of sponge iron carrier cores as in Example I.
- the carrier cores are mixed for about 10 minutes with about 1.0 part of powdered polyvinyl chloride and trifluorochloroethylene prepared from a material commercially available as FPC 461 from Firestone Plastics Company, Pottstown, Pa..
- the powdered coating material is attrited to an average particle diameter of less than about 44 microns.
- the dry mixture is placed in a muffle furnace and heated to a maximum temperature of 1 77 0 C cooled to room temperature over a total process time of about 75 minutes.
- Example I About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is unsatisfactory in that the triboelectric charge generated on the toner material is about 16 microcoulombs per gram of toner, the developed image background density is about 0.03, and the image quality is unacceptable.
- the electrical resistivity of the developer is about 1.5 x 10 ohm-cms.
- a carrier material is prepared in the following manner. About 50 grams of polyvinylidene fluoride and tetrafluoroethylene copolymer commercially available as Kynar 7201 from Pennwalt Corporation, King of Prussia, Pa. is placed in a heating vessel and brought to a fluid state. About 3 grams of carbon black commercially available as Ketjenblack - EC from Armak Corporation, Chicago, Illinois is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then cooled and allowed to solidify into a solid mass. The solid mass is then converted to dry, powdered particles having an average particle size of less than about 44 microns by cryogenic grinding using liquid nitrogen to cool the pigmented polymer composition and steel shot having a diameter of about 1/8 inch as a grinding aid.
- Example I About 99 parts of the sponge iron carrier cores described in Example I is mixed for about 10 minutes with about 1 part of the aforedescribed dry, powdered particles whereby the powdered coating composition electrostatically adheres to the carrier cores.
- the dry mixture is placed in a muffle furnace and heated to a maximum temperature of about 127° C and then cooled to room temperature over a total process time of about 15 minutes.
- Example II About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 25 microcoulombs per gram of toner material.
- the developed image background density is only about .008, and the image quality is excellent.
- the electrical resistivity of the developer is about 7.8 x 10 9 ohm-cms.
- a carrier material is prepared in the following manner. About 50 grams of polyvinylidene fluoride commercially available as Kynar 461 from Pennwalt Corporation, King of Prussia, Pa. is placed in a heating vessel and brought to a fluid state. About 5 grams of the carbon black of Example III is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then cooled and allowed to solidify into a solid mass. The solid mass is then converted to dry, powdered particles having an average particle size of less than about 44 microns by cryogenic grinding as in Example III.
- Example II About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 28 microcoulombs per gram of toner material.
- the developed image background is only about .006, and the image quality is excellent.
- the electrical resistivity of the developer is about 5.4 x 10 9 ohm-cms.
- a carrier material is prepared in the following manner. About 10 grams of polyvinylidene fluoride commercially available as Kynar 301 from Pennwalt Corporation, King of Prussia, Pa. is placed in a polyethylene jar containing about 2 grams of carbon black and about 250 ml of propylene carbonate solvent. The mixture is placed on a Red Devil paint shaker to disperse the pigment. Steel shot, 3.2mm diameter, is present in the mixture as a milling aid. After about 10 minutes of mixing, the mixture is sieved to remove the steel shot and the dispersion is put into a beaker and heated with stirring to about 85° C to dissolve the resin.
- Fine sized polyvinylidene fluoride coated carbon black particles are obtained of about 3 to 10 microns after filtration and washing with water.
- Example II About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 26 microcoulombs per gram of toner material.
- the developed image background density is only about .007, and the image quality is excellent.
- the electrical resistivity of the developer is about 1.3 x 10 9 ohm-cms.
- a carrier material is prepared in the following manner. About 50 grams of polyvinyl chloride and trifluorochloroethylene commercially available as FPC 461 from Firestone Plastics Company, Pottstown, Pa. is dissolved in about 300 mls of methyl ethyl ketone. About 4 grams of carbon black as in Example III is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then spray-dried to powdered particles having an average particle size of about 5 to 8 microns.
- Example II About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is . higher than that obtained with the developer mixture of Example II, being about 19 microcoulombs per gram of toner material.
- the developed image background density is only about .007, and the image quality is excellent.
- the electrical resistivity of the developer is about 8.7 x 10 9 ohm-cms.
- a carrier material is prepared in the following manner. About 50 grams of polyvinylidene fluoride and tetrafluoroethylene copolymer commercially available as Kynar 7201 from Pennwalt Corporation, King of Prussia, Pa. is placed in a heating vessel and brought to a fluid state. About 3 grams of phthalocyanine is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then cooled and allowed to solidify into a solid mass. The solid mass is then converted to dry, powdered particles having an average particle size of less than about 44 microns by cryogenic grinding as in Example Ill.
- Example I About 99 parts of the sponge iron carrier cores described in Example I is mixed for about 10 minutes with about 1 part of the aforedescribed dry, powdered particles whereby the powdered coating composition electrostatically adheres to the carrier cores.
- the dry mixture is placed in a muffle furnace and heated to a maximum temperature of about 127 0 C and then cooled to room temperature over a total process time of about 15 minutes.
- Example II About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 23 microcoulombs per gram of toner material.
- the developed image background density is only about .006, and the image quality is excellent.
- the electrical resistivity of the developer is about 9.2 x 10 9 ohm-cms.
- a carrier material is prepared in the following manner. About 50 grams of polyvinylidene fluoride commercially available as Kynar 201 from Pennwalt Corporation, King of Prussia, Pa. is placed in a heating vessel and brought to a fluid state. About 10 grams of aluminum commercially available as MD-796 from Alcan Metal Powders, Inc., of Elizabeth, New Jersey having an average particle size of less than about 45 microns is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then cooled and allowed to solidify into a solid mass. The solid mass is then converted to dry, powdered particles having an average particle size of less than about 50 microns by cryogenic grinding as in Example III.
- Example I About 98 parts of the sponge iron carrier cores described in Example I is mixed for about 10 minutes with about 2 parts of the aforedescribed dry, powdered particles whereby the powdered coating composition electrostatically adheres to the carrier cores.
- the dry mixture is placed in a muffle furnace and heated to a maximum temperature of about 2320C and then cooled to room temperature over a total process time of about 70 minutes.
- Example I About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 32 microcoulombs per gram of toner material.
- the developed image background density is satisfactory and the image quality is excellent.
- a carrier material is prepared in the following manner. About 50 grams of polyvinylidene fluoride commercially available as Kynar 201 from Pennwalt Corporation, King of Prussia, Pa. is placed in a heating vessel and brought to a fluid state. About 10 grams. of carbon black commercially available as Vulcan XC-72 from Cabot Corporation, Boston, Mass. is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then cooled and allowed to solidify into a solid mass. The solid mass is then converted to dry, powdered particles having an average particle size of less than about 44 microns by cryogenic grinding as in Example III.
- Example I About 98 parts of the sponge iron carrier cores described in Example I is mixed for about 10 minutes with about 2 parts of the aforedescribed dry, powdered particles whereby the powdered coating composition electrostatically adheres to the carrier cores.
- the dry mixture is placed in a muffle furnace and heated to a maximum temperature of about 232 0 c and then cooled to room temperature over a total process time of about 70 minutes.
- Example II About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 16 microcoulombs per gram of toner material.
- the developed image background density is satisfactory and the image quality is excellent
- a carrier material is prepared in the following manner. About 50 grams of vinyl chloride/vinyl acetate/maleic acid terpolymer commercially available as Vinylite VYNS from Union Carbide Corporation, New York, New York is placed in a heating vessel and brought to a fluid state. About 8 grams of carbon black as in Example IX is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then cooled and allowed to solidify into a solid mass. The solid mass is then converted to dry, powdered particles having an average particle size of less than about 44 microns by cryogenic grinding as in Example III.
- Example II About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 18 microcoulombs per gram of toner material.
- the developed image background density is satisfactory and the image quality is excellent.
- the electrical resistivity of the developer is about 7.6 x 10 9 ohm-cms.
- a carrier material is prepared in the following manner. About 50 grams of polyvinyl chloride and trifluorochloroethylene commercially available as FPC 461 from Firestone Plastics Company, Pottstown, Pa. is dissolved in about 300 mls of methyl ethyl ketone. About 4 grams of cetyl pyridinium chloride available from Hexcel Corporation, Lodi, New Jersey is added to the fluid resin composition and stirred therewith until a substantially uniform mixture is obtained. The mixture is then spray-dried to powdered particles having an average particle size of about 5 to 8 microns.
- Example I About 98 parts of the sponge iron carrier cores described in Example I is mixed for about 10 minutes with about 2 parts of the aforedescribed dry, powdered particles whereby the powdered coating composition electrostatically adheres to the carrier cores.
- the dry mixture is placed in a muffle furnace and heated to a maximum temperature of about 135 0 C and then cooled to room temperature over a total process time of about 30 minutes.
- Example I About 97 parts by weight of the coated carrier particles is mixed with about 3 parts by weight of toner particles as in Example I.
- the mixture of carrier and toner particles is employed as in Example I to develop an electrostatic latent image. It is found that this developer mixture is satisfactory in that the triboelectric charge generated on the toner material is higher than that obtained with the developer mixture of Example II, being about 18 microcoulombs per gram of toner material.
- the developed image background density is satisfactory and the image quality is excellent.
- thermoplastic toner resin components such as those listed above may be substituted for those in the examples with similar results.
- Other materials may also be added to the toner or carrier to sensitize, synergize or otherwise improve the fusing properties or other desirable properties of the system.
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US4548879A | 1979-06-04 | 1979-06-04 | |
US45488 | 1979-06-04 |
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EP0020181A1 true EP0020181A1 (en) | 1980-12-10 |
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Application Number | Title | Priority Date | Filing Date |
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EP80301870A Withdrawn EP0020181A1 (en) | 1979-06-04 | 1980-06-04 | Process for preparing coated carrier particles for electrostatographic developers |
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EP (1) | EP0020181A1 (ja) |
JP (1) | JPS55163544A (ja) |
BR (1) | BR8003338A (ja) |
CA (1) | CA1140784A (ja) |
ES (1) | ES492113A0 (ja) |
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EP0363900A3 (en) * | 1988-10-13 | 1990-06-27 | Daikin Industries, Limited | Carriers for developing electrostatic images |
EP0448030A1 (en) * | 1990-03-20 | 1991-09-25 | Konica Corporation | Resin coated carriers for electrostatic image development and the method of preparing the same |
EP0468811A3 (en) * | 1990-07-27 | 1992-03-18 | Konica Corporation | Carrier for developing electrostatic image |
EP0767412A1 (en) * | 1995-10-05 | 1997-04-09 | Nashua Corporation | A coated carrier particle containing a charge control agent |
GB2333975A (en) * | 1995-05-09 | 1999-08-11 | Colorcon Ltd | Electrostatic coating with powder material |
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US6783768B1 (en) | 1996-11-13 | 2004-08-31 | Phoqus Pharmaceuticals Limited | Method and apparatus for the coating of substrates for pharmaceutical use |
US7008668B2 (en) | 1995-05-09 | 2006-03-07 | Phoqus Pharmaceuticals Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
US7285303B2 (en) | 2000-02-01 | 2007-10-23 | Phoqus Pharmaceuticals Limited | Powder material for electrostatic application to a substrate and electrostatic application of the powder material to a substrate |
US7732020B2 (en) | 2004-03-31 | 2010-06-08 | Glaxo Group Limited | Method and apparatus for the application of powder material to substrates |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
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ES8305948A1 (es) * | 1980-12-24 | 1983-04-16 | Xerox Corp | Un metodo mejorado de formacion electrofotografica de imagenes o de formacion magnetica de imagenes. |
JPS60207150A (ja) * | 1984-03-30 | 1985-10-18 | Mita Ind Co Ltd | 二成分系現像剤用トナ− |
JP2710241B2 (ja) * | 1986-08-01 | 1998-02-10 | ミノルタ株式会社 | 静電潜像現像用キャリア及びその製造方法 |
JP2679724B2 (ja) * | 1986-08-01 | 1997-11-19 | ミノルタ 株式会社 | 静電潜像現像用キャリアおよびその製造方法 |
JPS63132255A (ja) * | 1986-11-21 | 1988-06-04 | Sharp Corp | 電子写真用トナ− |
JP2626754B2 (ja) * | 1987-05-14 | 1997-07-02 | 株式会社リコー | 乾式現剤像用キャリア |
JP2699373B2 (ja) * | 1988-02-10 | 1998-01-19 | 富士ゼロックス株式会社 | 電子写真用キャリア |
JPH01209455A (ja) * | 1988-02-17 | 1989-08-23 | Mitsubishi Kasei Corp | 電子写真用現像剤 |
JPH01211770A (ja) * | 1988-02-19 | 1989-08-24 | Mitsubishi Kasei Corp | 電子写真用現像剤 |
JPH0210375A (ja) * | 1988-06-29 | 1990-01-16 | Tomoegawa Paper Co Ltd | 正帯電性イエロー現像剤 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3533835A (en) * | 1966-10-11 | 1970-10-13 | Xerox Corp | Electrostatographic developer mixture |
GB1322623A (en) * | 1970-03-04 | 1973-07-11 | Exxon Research Engineering Co | Macroencapsulation of elastomeric or mastic polymers |
GB1437536A (en) * | 1972-07-26 | 1976-05-26 | Ato Chimie | Method and apparatus for the application of a coating of plastics material |
GB1535891A (en) * | 1976-01-23 | 1978-12-13 | Pitney Bowes Inc | Carrier for development powders used in electrophotographic copying |
-
1980
- 1980-04-08 CA CA000349309A patent/CA1140784A/en not_active Expired
- 1980-05-28 JP JP7131080A patent/JPS55163544A/ja active Pending
- 1980-05-28 BR BR8003338A patent/BR8003338A/pt unknown
- 1980-06-03 ES ES492113A patent/ES492113A0/es active Granted
- 1980-06-04 EP EP80301870A patent/EP0020181A1/en not_active Withdrawn
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3533835A (en) * | 1966-10-11 | 1970-10-13 | Xerox Corp | Electrostatographic developer mixture |
GB1322623A (en) * | 1970-03-04 | 1973-07-11 | Exxon Research Engineering Co | Macroencapsulation of elastomeric or mastic polymers |
GB1437536A (en) * | 1972-07-26 | 1976-05-26 | Ato Chimie | Method and apparatus for the application of a coating of plastics material |
GB1535891A (en) * | 1976-01-23 | 1978-12-13 | Pitney Bowes Inc | Carrier for development powders used in electrophotographic copying |
Non-Patent Citations (2)
Title |
---|
RESEARCH DISCLOSURE, No. 128, December 1974 Hampshire GB A.E. FIELDS et al.: "Electrographic carrier particles", pages 15-16 art. No. 12844 * Page 15, column 2, paragraph 8, the examples * * |
RESEARCH DISCLOSURE, No. 148, August 1976 Hampshire GB G.P. KASPER et al.: " A Process for coating carrier particles", pages 74-76, art. No. 14852 * Page 75, column 1, paragraphs 1-6; the examples * * |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0321709A3 (en) * | 1987-12-23 | 1990-04-04 | Francisco José Izundegui MacDonnell | Fast healing and binding chemical compound or curative agent for healing wounded live animal and human soft tissues inflicted by cutting edges or separating forces |
EP0360146A3 (en) * | 1988-09-22 | 1990-06-20 | Konica Corporation | Carrier for electrostatic image development and method of preparing it |
EP0363900A3 (en) * | 1988-10-13 | 1990-06-27 | Daikin Industries, Limited | Carriers for developing electrostatic images |
EP0448030A1 (en) * | 1990-03-20 | 1991-09-25 | Konica Corporation | Resin coated carriers for electrostatic image development and the method of preparing the same |
US5182181A (en) * | 1990-03-20 | 1993-01-26 | Konica Corporation | Resin coated carriers for electrostatic image development and the method of preparing the same |
EP0468811A3 (en) * | 1990-07-27 | 1992-03-18 | Konica Corporation | Carrier for developing electrostatic image |
GB2333975A (en) * | 1995-05-09 | 1999-08-11 | Colorcon Ltd | Electrostatic coating with powder material |
GB2333975B (en) * | 1995-05-09 | 2000-01-12 | Colorcon Ltd | Improvements in or relating to electrostatic coating of substrates |
US6406738B1 (en) | 1995-05-09 | 2002-06-18 | Phoqus Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
US7008668B2 (en) | 1995-05-09 | 2006-03-07 | Phoqus Pharmaceuticals Limited | Powder coating composition for electrostatic coating of pharmaceutical substrates |
US7070656B2 (en) | 1995-05-09 | 2006-07-04 | Phoqus Pharmaceuticals Limited | Electrostatic coating |
US5627001A (en) * | 1995-10-05 | 1997-05-06 | Nashua Corporation | Coated carrier particle containing a charge control agent |
EP0767412A1 (en) * | 1995-10-05 | 1997-04-09 | Nashua Corporation | A coated carrier particle containing a charge control agent |
US6783768B1 (en) | 1996-11-13 | 2004-08-31 | Phoqus Pharmaceuticals Limited | Method and apparatus for the coating of substrates for pharmaceutical use |
US7153538B2 (en) | 1996-11-13 | 2006-12-26 | Phoqus Pharmaceuticals Limited | Method and apparatus for the coating of substrates for pharmaceutical use |
US7285303B2 (en) | 2000-02-01 | 2007-10-23 | Phoqus Pharmaceuticals Limited | Powder material for electrostatic application to a substrate and electrostatic application of the powder material to a substrate |
US7732020B2 (en) | 2004-03-31 | 2010-06-08 | Glaxo Group Limited | Method and apparatus for the application of powder material to substrates |
Also Published As
Publication number | Publication date |
---|---|
ES8105489A1 (es) | 1981-06-01 |
ES492113A0 (es) | 1981-06-01 |
JPS55163544A (en) | 1980-12-19 |
CA1140784A (en) | 1983-02-08 |
BR8003338A (pt) | 1980-12-30 |
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