CA1140785A - Toner composition including carbon black and a copolymer of vinyl chloride and ethyl, propyl or butyl maleate - Google Patents
Toner composition including carbon black and a copolymer of vinyl chloride and ethyl, propyl or butyl maleateInfo
- Publication number
- CA1140785A CA1140785A CA000351553A CA351553A CA1140785A CA 1140785 A CA1140785 A CA 1140785A CA 000351553 A CA000351553 A CA 000351553A CA 351553 A CA351553 A CA 351553A CA 1140785 A CA1140785 A CA 1140785A
- Authority
- CA
- Canada
- Prior art keywords
- particles
- toner
- weight
- copolymer
- resin
- 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 abstract description 24
- 229920001577 copolymer Polymers 0.000 title claims abstract description 15
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims abstract description 9
- 239000006229 carbon black Substances 0.000 title claims description 7
- UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 title claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 title description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 title description 2
- 239000003086 colorant Substances 0.000 claims abstract description 12
- 239000002245 particle Substances 0.000 claims description 78
- 229920005989 resin Polymers 0.000 claims description 32
- 239000011347 resin Substances 0.000 claims description 32
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 claims description 6
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 claims description 6
- 229920006026 co-polymeric resin Polymers 0.000 claims description 3
- DSTWFRCNXMNXTR-WAYWQWQTSA-N dipropyl (z)-but-2-enedioate Chemical compound CCCOC(=O)\C=C/C(=O)OCCC DSTWFRCNXMNXTR-WAYWQWQTSA-N 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims 1
- -1 alkyl maleate Chemical compound 0.000 abstract description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract description 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract description 3
- 239000011521 glass Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- 238000012360 testing method Methods 0.000 description 11
- 239000011324 bead Substances 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 238000011161 development Methods 0.000 description 6
- 230000018109 developmental process Effects 0.000 description 6
- 230000009477 glass transition Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- 238000006722 reduction reaction Methods 0.000 description 5
- 239000012260 resinous material Substances 0.000 description 5
- 238000001694 spray drying Methods 0.000 description 5
- 229910000859 α-Fe Inorganic materials 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 238000010951 particle size reduction Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000005549 size reduction Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000012876 carrier material Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 3
- 230000005291 magnetic effect Effects 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 208000036366 Sensation of pressure Diseases 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 235000012771 pancakes Nutrition 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene 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
- 239000006230 acetylene black Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000003849 aromatic solvent 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
- 230000008901 benefit Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007334 copolymerization reaction 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
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 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
- 239000000696 magnetic material Substances 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 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
- 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
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 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
- 229920002981 polyvinylidene fluoride Polymers 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
- 238000011084 recovery Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000007864 suspending Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 229920006163 vinyl copolymer Polymers 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
- 239000008096 xylene Substances 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
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08726—Polymers of unsaturated acids or derivatives thereof
- G03G9/08731—Polymers of nitriles
-
- 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
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08713—Polyvinylhalogenides
- G03G9/08715—Polyvinylhalogenides containing chlorine, bromine or iodine
- G03G9/08717—Polyvinylchloride
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
An electrostatographic toner composition com-prising a colorant and a copolymer of from about 65 mol percent to about 75 mol percent vinyl chloride and from about 25 mol percent to about 35 mol percent of a lower alkyl maleate or fumarate, the copolymer having a number average molecular weight of from about 15,000 to about 25,000 and a weight average molecular weight of from about 45,000 to about 55,000.
An electrostatographic toner composition com-prising a colorant and a copolymer of from about 65 mol percent to about 75 mol percent vinyl chloride and from about 25 mol percent to about 35 mol percent of a lower alkyl maleate or fumarate, the copolymer having a number average molecular weight of from about 15,000 to about 25,000 and a weight average molecular weight of from about 45,000 to about 55,000.
Description
4Q~S
TONER COMPOSITION OF VINYL COPOLYMER
BACKGROUND OF THE INVENTION
This invention relates to toner compositions for use in developing latent electrostatographic images and more particularly to toner compositions which exhibit long life in the electrostatographic process.
In the development of electrostatographic images, a toner composition is mixed with a carrier composition in order to impart the proper charge charac-teristics to the toner particles and also for the purpose of carrying the toner particles by a physical means to the surface which contains the latent electrostatic image. The carrier particles are generally much larger in particle size than that of the toner varying from perhaps 5 to 100 times larger depending upon the parti-cular developer being employed. The toner is thus sub-jected to large forces in the development housing and
TONER COMPOSITION OF VINYL COPOLYMER
BACKGROUND OF THE INVENTION
This invention relates to toner compositions for use in developing latent electrostatographic images and more particularly to toner compositions which exhibit long life in the electrostatographic process.
In the development of electrostatographic images, a toner composition is mixed with a carrier composition in order to impart the proper charge charac-teristics to the toner particles and also for the purpose of carrying the toner particles by a physical means to the surface which contains the latent electrostatic image. The carrier particles are generally much larger in particle size than that of the toner varying from perhaps 5 to 100 times larger depending upon the parti-cular developer being employed. The toner is thus sub-jected to large forces in the development housing and
2~ in transit toward the imaging surface, which forces result in the particle size reduction of the toner par-ticles. This creates problems because it not only pro-vides a source for dirt made up o~ the fine toner par-ticles but also changes the triboelectric character of the toner particles because of the reduction in size thereof and the impaction and adhesion to the carrier particles. On the other hand, ~or economic reasons it is desired to use customary particle size reduction techniques to achieve the desired particle size of the colorant filled resinous materials. Uni~ormity in particle size can be achieved subsequent to size reduc-tion by standard classification methods. A problem encountered because of these objecti~es is that particle size reduction will also occur in the electrostatographic apparatus because the conditions therein are similar to that encountered in the size reduction apparatus.
,~;
7~5 Thus, brittle failure of the toner particles together with size reduction occurs in the electrostatographic process. This size reduction during the electrostato-graphic process results in changes in both the tribo-electric and charging characteristics of the toner par-ticles with respect to the particular carrier materials employed in the process. That is, as the particle size reduction of the toner particles occurs, the charge to mass ratio on the particles increases thereby increasing the forces holding the size reduced toner particles to the carrier particles. This results in even more harsh impacts between the large size carrier particles and the toner particles either causing further reduction in the particle sizes or flattening of the particles out in a pancake fashion which tightly adhere to the surface of the carrier particles eventually resulting in reduction in the triboelectric characteristics.
PRIOR ART STATEME~T
The following prior art appears to be perti-20 nent:
Maclay 3,391,082 July 2, 1969 Sadamatsu et al 3,941,898 March 2, 1976 Clemens et al 3,965,021 June ~0, 1967 The Maclay patent discloses a xerographic toner wherein the resin has a second order glass transition te~perature of 30 to 65C and a limiting viscosity of 0.15 to 0.35. The resin is prepared as a latex in the presence of an organic chain transfer agent by the cata-lytic polymerization in aqueous emulsion of a monomer mixture of a hard monomer component and a soft monomer component.
The Sadamatsu et al patent relates to a xero-graphic developing method using as the toner, a cross linked polymer of controlled molecular weight prepared by polymerizing in the presence of a crosslinking agent and a material capable of controlling the molecular ~Q7~
weight, mixing with a coloring material and pulverizing the obtained mixture.
The Clemens et al patent ~3,965,021) is directed to a toner wherein the resinous material is a blend o~ at least two polymers the first having a glass transition temperature of at least 20C and the second a glass transition temperature at least 5 lower than that of the first polymer.
SUMMARY OF THE INVENTION
An aspect of the invention is as follows:
An improved electrostatographic tough powdered toner composition consisting essentially of a resin in an amount of 85 percent by weight to 98 percent by weight, the resin being a copolymer containing 65 to 75 mol percent o vinyl chloride and 25 to 35 mol percent of ethyl maleate, propyl maleate, or butyl maleate, said copolymer having a number average molecular weight of from about 15,000 to about 25,000 and a weight average molecular weight from about 45,000 to about 55,000, and contain-ing as a colorant carbon black in an amount of from about 2% to 15~ by ~eight, the toner particles ranging in size of from about 1 micron to about 20 microns.
These particular copolymers exhibit extraordinary toughness and long life in the development of electrostatic latent images while at the same time offer extremely good fusing characteristics and excellent blocking characteristics during storage, shipping and in the development procedure of the electrostatographic machine.
The colorant is employed in an amount of from about two weight percent to about 15 weight percent, based on the weight of the toner and preferably from about four percent to about ten percent. A particular advantage achieved using the vinyl polymer in accordance with this invention is that sharp, dark images are obtained using 5 percent by weight carbon black which is only about one-half the amount used in commercially available compositions.
7~S
In the practice of this invention, any suitable vinyl chloride - lower alkyl maleate or lower alkyl fumarate copolymer in the quantities set forth above, may be used in the preparation of the copolymer such as, for example, the C2 to C4 esters of maleic acid and fumaric acid such as ethyl, diethyl, propyl, isopropyl, dipropyl, diisopropyl, butyl, isobutyl, tertiary butyl, dibutyl diisobutyl, ditertiary butyl and the like. Ethyl maleate and diethyl maleate are the preferred monomers for copolymerization with vinyl chloride.
The copolymers used in the preparation of toner compositions in accordance with this invention are gene-rally prepared by suspension polymerization techniques which are well known in the art. In this method, the monomers are mi~ed together with a suitable catalyst, such as benzoyl peroxide, lauroyl peroxide, azoisobuty-rylnitrile and the like and dispersed with agitation as droplets (discontinuous phase) in an aqueous medium (continuous phase) which contains stabilizers, emulsifiers and the like.
The polymer should have a suitable molecular weight such that when toner size particles are prepared, they will have sufficient toughness to withstand the vigorous environment within an electrostatographic ap-paratus, while at the same time exhibit the rheologicalproper~ies that prevents blocking under storage and transport conditions but can be readily fixed to paper substrates by normal fusing conditions.
The toughness of the toner si~e particles can readily be determined by simulating conditions in an electrostatographic machine. This can be done in a roll mill wherein the resin powder is rolled with a carrier material over a period of time and by visual observation of the toner particles under a scanning electron micro-scope.
1~iL40~7~35 The blocking characteristics oE the resin canbe determined by measurement of the second order glass transition temperature. This generally should be as high as possible without interfering with the fusing requirements. This second ord~r glass transition tem-perature should preferably be from about 41 ~o 65C and preferably from about 54C to about 63C at a heating rate of 10C per minute in a Differential Scanning Calo-rimeter.
The fusing characteristics can be determined simply by placing particles of the toner size using particles on a glass slide in an oven preheated to 135C
for two minutes. The particles, if satisfactory for toner, will coalesce within this time.
In a specific test for toughness of the resin, six grams of resin powder made up of resin particles having a size of from about 10 to 15 micron are rolled in a glass jar of 473 cubic centimeters at a rate of 27.5 linear meters per minute with 500 grams of 250 micron coated glass beads having a density of about 4.2 grams per cubic centimeter, which are uniformly coated to a thickness of from 0.25 to 1 micron with a copolymer of about 48 mol percent chlorotrifluoroethylene and about 52 mol percent of vinyl chloride sold by Firestone Plastics Company under the designation FPC461. Samples are withdrawn periodically and the resin powder is blown off the coated glass beads with an airstream at a pres-sure of 4.57 kilograms per cubic centimeter.
The blown off powder is viewed under a scanning electron microscope and a comparison is made with the original particles. The longer the rolling test can be conducted without a difference being observed, the tougher is the resin. That is, one viewing the resin particles after the rolling test should be unable to detect any substantial number of particles which have cracks or have been reduced in particle size because ~Q7~
of brittle failure caused by impaction with the high density glass beads.
T~e rolling test, set forth above can also be used in conjunction with a test for resin powder concentration and charge to mass ratio. In this test, the rolled resin particles and carrier particles are placed in a Faraday Cage and dry compressed air is blown through the cage under a pressure of 4.57 kg/cm in order to remove all of the resin particles capable of being removed from the coated glass beadsO A Faraday Cage is a device which consists of a brass cylinder having a diameter of one inch and a length of one inch. A lO0 mesh screen is positioned at each end of the cylinder.
The cylinder is weighed, charged with 0.5 grams of the above stated mixture and connected to ground through a capacitor and an electrometer connected in parallel.
In addition to the determination of the resin concen-tration or the weight loss by impaction on the glass carrier beads, this device also is used to determine the charge on the particles in microcoulombs per gram of resin po~der. The weight loss of the resin sample can occur by two modes of resin particle failure, either of which will be determined by the tests set forth above.
First, the particles can fail by brittle fracture, thereby causing the attrition of the resin particles with the accompanying reduction in the mass of the resulting particles. This reduction in mass corresponds to an increase in the charge to mass ratio, thereby increasing the attractive forces between the coated glass beads and the size reduced resin particles. As the charge to mass ratio on the resin powder particles increases above 40 microcoulombs per gram, the attractive forces between the particles become so great that the resin particles and the glass bead particles become inseparable due to ~he action of the high pressure air passed through the Faraday Cage.
Secondly, the resin particles can fail because of ductile deformation. In this mode of failure, the resin particles become flattened against the surface o~ the larger high density glass beads in a pancake type formation. In such action, the particles literally become welded to the surface of the glass beads thus preventing blowoff and recovery of the toner particles.
It can be seen that the tests indicated above, that is, the visual observation oE the toner particles by scanning electron microscope and also the measurement of the recoverable toner after blowoff gives a precise test for determining whether a resin material will have the proper physical characteristics to withstand the forces involved in the normal operation of an electrostatographic apparatus.
In the practice of this invention, any suitable blend of esterified polymers as described above may be used in the preparation of toner particles by combining with a suitable colorant. The toner may be prepared by dissolving the resinous material and a coloring agent such as a dye or a pigment or by dissolving the resin and dispersing the colorant, should it be insoluble, in a suitable solvent and spray drying to achieve uni-formly siæed toner particles. The toner size may vary from about 1 micron to about 20 microns and preferably from about 10 to about 15 microns. The toner particles should be of substantially uniform si~e because of the nature of the spray drying operation.
In the preparation of the toner material, any suitable colorant may he employed such as, for example, pigments or dyes including, 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 O~ylate, lamp black, Rose Bengal and other pigments and dyes set orth in the Color Index, Vols. I and II, ~econd Edition.
Should a magnetic toner be desired, the colorant may be a magnetic material such as iron particles, iron oxide, nickel, ferrite, magnetite or mixtures of magnetic particles and colorant.
In the preparation for spray drying, the re-sinous material employed in the colorant is dissolved in any suitable solvent such as, for example, chlorinated so-vents including trichloroethane, methylene chloride, tetrachlorethane, methylene dichloride, chloroform, aromatic solvents such as toluene, benzene, naphthalene, xylene, ketones such as, for example, methylethyl ketone, acetone, esters such as ethylacetate, amylacetate, mix-tures thereof and the like. The solvent should be chosen in order to assure that all the resin components are soluble.
The spray drying operation is conducted in a suitable spray drying apparatus such as, for example, the Bowen Laboratory spray dryer manufactured by Bowen Engineering Corporation, North Branch, New Jersey. This unit is a lab size conical dryer with concurrent airflow and has an interchangable atomizing head mounted near the top of the drying chamber. Any suitable atomizing head may be employed such as, rotating disks, high pres-sure noxzles and the like. In order to achieve uniformity in size of the particles, it may be desirable to classify the particles by any suitable classification techniques well known in the classification art.
The toners of this invention can be mixed with a suitable carrier to form electrostatographic developers.
Any suitable carriers having a particle size of from about 30 microns to about 1,000 microns may be employed such as, ~or example, glass beads, sand, particles of ferromagnetic materials such as iron, cobalt, nickel, allo~s thereof~ ferrites, and the like. Resinous mate-rials such as methylmethacrylate, styrene and any suitable resinous materials in particle sixes set forth ~40~ 515 g above. The carriers may be employed with or without a coating. Many suitable resinous coating materials may be employed such as polyolefins, such as polyethylene polymethyl styrene, polymethylmethacrylate, polyacryl-onitrile, polyvinylacetate polyvinyl alcohol, polyvinyl carbazole, fluorocarbons, such as polytetrafluorethylene, polyvinylidene fluoride, polyamides, polyurethanes, polycarbonates and the polymers set forth in U.S. Patent
,~;
7~5 Thus, brittle failure of the toner particles together with size reduction occurs in the electrostatographic process. This size reduction during the electrostato-graphic process results in changes in both the tribo-electric and charging characteristics of the toner par-ticles with respect to the particular carrier materials employed in the process. That is, as the particle size reduction of the toner particles occurs, the charge to mass ratio on the particles increases thereby increasing the forces holding the size reduced toner particles to the carrier particles. This results in even more harsh impacts between the large size carrier particles and the toner particles either causing further reduction in the particle sizes or flattening of the particles out in a pancake fashion which tightly adhere to the surface of the carrier particles eventually resulting in reduction in the triboelectric characteristics.
PRIOR ART STATEME~T
The following prior art appears to be perti-20 nent:
Maclay 3,391,082 July 2, 1969 Sadamatsu et al 3,941,898 March 2, 1976 Clemens et al 3,965,021 June ~0, 1967 The Maclay patent discloses a xerographic toner wherein the resin has a second order glass transition te~perature of 30 to 65C and a limiting viscosity of 0.15 to 0.35. The resin is prepared as a latex in the presence of an organic chain transfer agent by the cata-lytic polymerization in aqueous emulsion of a monomer mixture of a hard monomer component and a soft monomer component.
The Sadamatsu et al patent relates to a xero-graphic developing method using as the toner, a cross linked polymer of controlled molecular weight prepared by polymerizing in the presence of a crosslinking agent and a material capable of controlling the molecular ~Q7~
weight, mixing with a coloring material and pulverizing the obtained mixture.
The Clemens et al patent ~3,965,021) is directed to a toner wherein the resinous material is a blend o~ at least two polymers the first having a glass transition temperature of at least 20C and the second a glass transition temperature at least 5 lower than that of the first polymer.
SUMMARY OF THE INVENTION
An aspect of the invention is as follows:
An improved electrostatographic tough powdered toner composition consisting essentially of a resin in an amount of 85 percent by weight to 98 percent by weight, the resin being a copolymer containing 65 to 75 mol percent o vinyl chloride and 25 to 35 mol percent of ethyl maleate, propyl maleate, or butyl maleate, said copolymer having a number average molecular weight of from about 15,000 to about 25,000 and a weight average molecular weight from about 45,000 to about 55,000, and contain-ing as a colorant carbon black in an amount of from about 2% to 15~ by ~eight, the toner particles ranging in size of from about 1 micron to about 20 microns.
These particular copolymers exhibit extraordinary toughness and long life in the development of electrostatic latent images while at the same time offer extremely good fusing characteristics and excellent blocking characteristics during storage, shipping and in the development procedure of the electrostatographic machine.
The colorant is employed in an amount of from about two weight percent to about 15 weight percent, based on the weight of the toner and preferably from about four percent to about ten percent. A particular advantage achieved using the vinyl polymer in accordance with this invention is that sharp, dark images are obtained using 5 percent by weight carbon black which is only about one-half the amount used in commercially available compositions.
7~S
In the practice of this invention, any suitable vinyl chloride - lower alkyl maleate or lower alkyl fumarate copolymer in the quantities set forth above, may be used in the preparation of the copolymer such as, for example, the C2 to C4 esters of maleic acid and fumaric acid such as ethyl, diethyl, propyl, isopropyl, dipropyl, diisopropyl, butyl, isobutyl, tertiary butyl, dibutyl diisobutyl, ditertiary butyl and the like. Ethyl maleate and diethyl maleate are the preferred monomers for copolymerization with vinyl chloride.
The copolymers used in the preparation of toner compositions in accordance with this invention are gene-rally prepared by suspension polymerization techniques which are well known in the art. In this method, the monomers are mi~ed together with a suitable catalyst, such as benzoyl peroxide, lauroyl peroxide, azoisobuty-rylnitrile and the like and dispersed with agitation as droplets (discontinuous phase) in an aqueous medium (continuous phase) which contains stabilizers, emulsifiers and the like.
The polymer should have a suitable molecular weight such that when toner size particles are prepared, they will have sufficient toughness to withstand the vigorous environment within an electrostatographic ap-paratus, while at the same time exhibit the rheologicalproper~ies that prevents blocking under storage and transport conditions but can be readily fixed to paper substrates by normal fusing conditions.
The toughness of the toner si~e particles can readily be determined by simulating conditions in an electrostatographic machine. This can be done in a roll mill wherein the resin powder is rolled with a carrier material over a period of time and by visual observation of the toner particles under a scanning electron micro-scope.
1~iL40~7~35 The blocking characteristics oE the resin canbe determined by measurement of the second order glass transition temperature. This generally should be as high as possible without interfering with the fusing requirements. This second ord~r glass transition tem-perature should preferably be from about 41 ~o 65C and preferably from about 54C to about 63C at a heating rate of 10C per minute in a Differential Scanning Calo-rimeter.
The fusing characteristics can be determined simply by placing particles of the toner size using particles on a glass slide in an oven preheated to 135C
for two minutes. The particles, if satisfactory for toner, will coalesce within this time.
In a specific test for toughness of the resin, six grams of resin powder made up of resin particles having a size of from about 10 to 15 micron are rolled in a glass jar of 473 cubic centimeters at a rate of 27.5 linear meters per minute with 500 grams of 250 micron coated glass beads having a density of about 4.2 grams per cubic centimeter, which are uniformly coated to a thickness of from 0.25 to 1 micron with a copolymer of about 48 mol percent chlorotrifluoroethylene and about 52 mol percent of vinyl chloride sold by Firestone Plastics Company under the designation FPC461. Samples are withdrawn periodically and the resin powder is blown off the coated glass beads with an airstream at a pres-sure of 4.57 kilograms per cubic centimeter.
The blown off powder is viewed under a scanning electron microscope and a comparison is made with the original particles. The longer the rolling test can be conducted without a difference being observed, the tougher is the resin. That is, one viewing the resin particles after the rolling test should be unable to detect any substantial number of particles which have cracks or have been reduced in particle size because ~Q7~
of brittle failure caused by impaction with the high density glass beads.
T~e rolling test, set forth above can also be used in conjunction with a test for resin powder concentration and charge to mass ratio. In this test, the rolled resin particles and carrier particles are placed in a Faraday Cage and dry compressed air is blown through the cage under a pressure of 4.57 kg/cm in order to remove all of the resin particles capable of being removed from the coated glass beadsO A Faraday Cage is a device which consists of a brass cylinder having a diameter of one inch and a length of one inch. A lO0 mesh screen is positioned at each end of the cylinder.
The cylinder is weighed, charged with 0.5 grams of the above stated mixture and connected to ground through a capacitor and an electrometer connected in parallel.
In addition to the determination of the resin concen-tration or the weight loss by impaction on the glass carrier beads, this device also is used to determine the charge on the particles in microcoulombs per gram of resin po~der. The weight loss of the resin sample can occur by two modes of resin particle failure, either of which will be determined by the tests set forth above.
First, the particles can fail by brittle fracture, thereby causing the attrition of the resin particles with the accompanying reduction in the mass of the resulting particles. This reduction in mass corresponds to an increase in the charge to mass ratio, thereby increasing the attractive forces between the coated glass beads and the size reduced resin particles. As the charge to mass ratio on the resin powder particles increases above 40 microcoulombs per gram, the attractive forces between the particles become so great that the resin particles and the glass bead particles become inseparable due to ~he action of the high pressure air passed through the Faraday Cage.
Secondly, the resin particles can fail because of ductile deformation. In this mode of failure, the resin particles become flattened against the surface o~ the larger high density glass beads in a pancake type formation. In such action, the particles literally become welded to the surface of the glass beads thus preventing blowoff and recovery of the toner particles.
It can be seen that the tests indicated above, that is, the visual observation oE the toner particles by scanning electron microscope and also the measurement of the recoverable toner after blowoff gives a precise test for determining whether a resin material will have the proper physical characteristics to withstand the forces involved in the normal operation of an electrostatographic apparatus.
In the practice of this invention, any suitable blend of esterified polymers as described above may be used in the preparation of toner particles by combining with a suitable colorant. The toner may be prepared by dissolving the resinous material and a coloring agent such as a dye or a pigment or by dissolving the resin and dispersing the colorant, should it be insoluble, in a suitable solvent and spray drying to achieve uni-formly siæed toner particles. The toner size may vary from about 1 micron to about 20 microns and preferably from about 10 to about 15 microns. The toner particles should be of substantially uniform si~e because of the nature of the spray drying operation.
In the preparation of the toner material, any suitable colorant may he employed such as, for example, pigments or dyes including, 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 O~ylate, lamp black, Rose Bengal and other pigments and dyes set orth in the Color Index, Vols. I and II, ~econd Edition.
Should a magnetic toner be desired, the colorant may be a magnetic material such as iron particles, iron oxide, nickel, ferrite, magnetite or mixtures of magnetic particles and colorant.
In the preparation for spray drying, the re-sinous material employed in the colorant is dissolved in any suitable solvent such as, for example, chlorinated so-vents including trichloroethane, methylene chloride, tetrachlorethane, methylene dichloride, chloroform, aromatic solvents such as toluene, benzene, naphthalene, xylene, ketones such as, for example, methylethyl ketone, acetone, esters such as ethylacetate, amylacetate, mix-tures thereof and the like. The solvent should be chosen in order to assure that all the resin components are soluble.
The spray drying operation is conducted in a suitable spray drying apparatus such as, for example, the Bowen Laboratory spray dryer manufactured by Bowen Engineering Corporation, North Branch, New Jersey. This unit is a lab size conical dryer with concurrent airflow and has an interchangable atomizing head mounted near the top of the drying chamber. Any suitable atomizing head may be employed such as, rotating disks, high pres-sure noxzles and the like. In order to achieve uniformity in size of the particles, it may be desirable to classify the particles by any suitable classification techniques well known in the classification art.
The toners of this invention can be mixed with a suitable carrier to form electrostatographic developers.
Any suitable carriers having a particle size of from about 30 microns to about 1,000 microns may be employed such as, ~or example, glass beads, sand, particles of ferromagnetic materials such as iron, cobalt, nickel, allo~s thereof~ ferrites, and the like. Resinous mate-rials such as methylmethacrylate, styrene and any suitable resinous materials in particle sixes set forth ~40~ 515 g above. The carriers may be employed with or without a coating. Many suitable resinous coating materials may be employed such as polyolefins, such as polyethylene polymethyl styrene, polymethylmethacrylate, polyacryl-onitrile, polyvinylacetate polyvinyl alcohol, polyvinyl carbazole, fluorocarbons, such as polytetrafluorethylene, polyvinylidene fluoride, polyamides, polyurethanes, polycarbonates and the polymers set forth in U.S. Patent
3,52~,533. Many of the foregoing and other typical 1~ carriers are described in U.S. Patent Numbers 2,638,416;
2,618,552 and 4,075,3~1. The carrier sbould be chosen in order that the charge to mass ratio of the blown-off toner is Erom about 10 to about 40 micro coulombs/gram and preferably from about 10 to 30 micro coulombs/gm.
The toner composition generally comprises from about 0.1 to about 15 percent by weight of the total toner carrier weight. Preferably, the toner is present in an amount of from about 0.5 to 5 percent by weight based on the total weight of the developer mixture.
In addition to the presence of toner and car-rier, because the toner particles are prepared by spray dryin~, it is generally preferred to add a flow agent ; to the developing mixture in order to obtain the optimum flow characteristics of the toner in the electrostato-graphic system. Any suitable flow agent such as, for example, colloidal silica, aluminum oxide, titanium dioxide, talc and the like may be employed. These flow aids are sub-micron in size and preferably from about O O
50A to about 500A microns. The flow agents are added in an amount of from about 0.05 to about 1% based on the weight of the toner, and preferably from about 0.1 to about 0.5%.
The invention is further illustrated by the following examples in which parts and percentages are by weight unless otherwise specified.
EXA~5PLE I
A copolymer of about 70 mol percent vinyl chloride and about 30 mol percent ethyl maleate having a second order glass transition temperature (Tg) of 57C, a number of average molecular weight of about 21,750 and a wei~ht average molecular ~eight of about 51,350 by Gel Permeation Chromatography and marketed by Fire-stone Plastics under the grade designation FPC-471 is spray dried from a chloroform solution in a Bowen Labora-tory Spray Dryer to obtain copolymer resin particlesof from about 10 to 15 microns.
A small quantity of the resin particles are sprinkled onto a glass slide and placed in an oven pre-heated to 135C for two minutes. Upon removal, visual observation readily indicates that the particles coalesce.
Six grams of the spray dried particles are subjected to the roll mill test previously described herein. After 500 hours, the particles are viewed under a scanning electron microscope. No particle failure can be observed. Substantially 100% of the particles are recovered after blow-off.
EXAMPLE II
A solution of the ~opolymer of Example I in chloroform having 5~ carbon black dispersed therein is spray dried to form toner particles having a volume average particle size of about 13 microns and a number average particle size of about 4 to 5 microns and a resin content of about 95 percent and carbon black content of about 5 percent. About 0.25 percent of hydrophobic fumed silica sold as Aerosil~R972 by DeGussa Incorporated is blended into the toner in a Lodige Blender.
An electrostatic developer is prepared by mixin~ 1 percent of the above mixture with a carrier material of 100 micron ferrite particles coated with 1.2 percent, based on the weight of the ferrite, of a polystyrene resin having a number average molecular ~ zAD e J~ J ~
~40~5 weight of about 160,000 and a weight average molecular weight of about 360,000. The polystyrene resin contains about 25~ acetylene black. The coating is applied to the carrier core in a Wurster Spouting Fluidized Bed manufactured by Dairy Equipment Company, Madison/
Wisconsin. The ferrite core is prepared in accordance with Example II of U.S. Patent 4,075,391.
This developer is used in an electrostatographic copier having a magnetic brush development system. After 250,000 copies, no change is visible in copy quality or in the character of the toner particles viewed under a scanning electron microscope. Further, throughout the test, the charge to mass ratio on the toner and the toner concentration after blow-off remain substantially constant. The former being about 30 microcoulombs per gram.
EXAMPLE III
A copolymer of 72 mol percent vinyl chloride and 28 mol percent dibutyl maleate is prepared by sus-pending about 100 parts of the monomers in the statedratio and about 5 parts of lauroyl peroxide in about 500 parts by volume of a 1.25 percent polyvinyl alcohol-water solution which is agitated at 3000 r.p.m. ~or 30 seconds in a Waring Blender equipped with a Polytron mixing head to produce a droplet dispersion, the droplets having an average droplet size of about 12 microns.
The reaction is continued at about 70C with stirring at 80 r.p.m. for about six hours.
The polymer particles are separated by pouring the reaction mass into a large quantity of water and then centrifuging. The supernatatent liquid is decanted and the reaction product is washed three times with water.
The polymer thus formed is used in the pro-cedure of Bxample II to prepare toner particles anddeveloper.
~1~0~
This developer when used in an electrostato-graphic machine equipped with a magnetic brush develop-ment system gives excellent results over many copy cycles.
EXAMPLE IV
The procedure of Example III is repeated using diethyl maleate in place of dibutyl maleate. The re-sulting developer exhibits long life in a xerographic copier.
It is to be understood that the examples herein are by way of illustration and that other suitable co-polymers as indicated above may be used throughout for those specifically employed.
2,618,552 and 4,075,3~1. The carrier sbould be chosen in order that the charge to mass ratio of the blown-off toner is Erom about 10 to about 40 micro coulombs/gram and preferably from about 10 to 30 micro coulombs/gm.
The toner composition generally comprises from about 0.1 to about 15 percent by weight of the total toner carrier weight. Preferably, the toner is present in an amount of from about 0.5 to 5 percent by weight based on the total weight of the developer mixture.
In addition to the presence of toner and car-rier, because the toner particles are prepared by spray dryin~, it is generally preferred to add a flow agent ; to the developing mixture in order to obtain the optimum flow characteristics of the toner in the electrostato-graphic system. Any suitable flow agent such as, for example, colloidal silica, aluminum oxide, titanium dioxide, talc and the like may be employed. These flow aids are sub-micron in size and preferably from about O O
50A to about 500A microns. The flow agents are added in an amount of from about 0.05 to about 1% based on the weight of the toner, and preferably from about 0.1 to about 0.5%.
The invention is further illustrated by the following examples in which parts and percentages are by weight unless otherwise specified.
EXA~5PLE I
A copolymer of about 70 mol percent vinyl chloride and about 30 mol percent ethyl maleate having a second order glass transition temperature (Tg) of 57C, a number of average molecular weight of about 21,750 and a wei~ht average molecular ~eight of about 51,350 by Gel Permeation Chromatography and marketed by Fire-stone Plastics under the grade designation FPC-471 is spray dried from a chloroform solution in a Bowen Labora-tory Spray Dryer to obtain copolymer resin particlesof from about 10 to 15 microns.
A small quantity of the resin particles are sprinkled onto a glass slide and placed in an oven pre-heated to 135C for two minutes. Upon removal, visual observation readily indicates that the particles coalesce.
Six grams of the spray dried particles are subjected to the roll mill test previously described herein. After 500 hours, the particles are viewed under a scanning electron microscope. No particle failure can be observed. Substantially 100% of the particles are recovered after blow-off.
EXAMPLE II
A solution of the ~opolymer of Example I in chloroform having 5~ carbon black dispersed therein is spray dried to form toner particles having a volume average particle size of about 13 microns and a number average particle size of about 4 to 5 microns and a resin content of about 95 percent and carbon black content of about 5 percent. About 0.25 percent of hydrophobic fumed silica sold as Aerosil~R972 by DeGussa Incorporated is blended into the toner in a Lodige Blender.
An electrostatic developer is prepared by mixin~ 1 percent of the above mixture with a carrier material of 100 micron ferrite particles coated with 1.2 percent, based on the weight of the ferrite, of a polystyrene resin having a number average molecular ~ zAD e J~ J ~
~40~5 weight of about 160,000 and a weight average molecular weight of about 360,000. The polystyrene resin contains about 25~ acetylene black. The coating is applied to the carrier core in a Wurster Spouting Fluidized Bed manufactured by Dairy Equipment Company, Madison/
Wisconsin. The ferrite core is prepared in accordance with Example II of U.S. Patent 4,075,391.
This developer is used in an electrostatographic copier having a magnetic brush development system. After 250,000 copies, no change is visible in copy quality or in the character of the toner particles viewed under a scanning electron microscope. Further, throughout the test, the charge to mass ratio on the toner and the toner concentration after blow-off remain substantially constant. The former being about 30 microcoulombs per gram.
EXAMPLE III
A copolymer of 72 mol percent vinyl chloride and 28 mol percent dibutyl maleate is prepared by sus-pending about 100 parts of the monomers in the statedratio and about 5 parts of lauroyl peroxide in about 500 parts by volume of a 1.25 percent polyvinyl alcohol-water solution which is agitated at 3000 r.p.m. ~or 30 seconds in a Waring Blender equipped with a Polytron mixing head to produce a droplet dispersion, the droplets having an average droplet size of about 12 microns.
The reaction is continued at about 70C with stirring at 80 r.p.m. for about six hours.
The polymer particles are separated by pouring the reaction mass into a large quantity of water and then centrifuging. The supernatatent liquid is decanted and the reaction product is washed three times with water.
The polymer thus formed is used in the pro-cedure of Bxample II to prepare toner particles anddeveloper.
~1~0~
This developer when used in an electrostato-graphic machine equipped with a magnetic brush develop-ment system gives excellent results over many copy cycles.
EXAMPLE IV
The procedure of Example III is repeated using diethyl maleate in place of dibutyl maleate. The re-sulting developer exhibits long life in a xerographic copier.
It is to be understood that the examples herein are by way of illustration and that other suitable co-polymers as indicated above may be used throughout for those specifically employed.
Claims (3)
1. An improved electrostatographic tough powdered toner composition consisting essentially of a resin in an amount of 85 percent by weight to 98 percent by weight, the resin being a copolymer containing 65 to 75 mol percent of vinyl chloride and 25 to 35 mol percent of ethyl maleate, propyl maleate, or butyl maleate, said copolymer having a number average molecular weight of from about 15,000 to about 25,000 and a weight average molecular weight from about 45,000 to about 55,000, and contain-ing as a colorant carbon black in an amount of from about 2% to 15% by weight, the toner particles ranging in size of from about 1 micron to about 20 microns.
2. An electrostatographic toner composition in accordance with claim 1 characterized in that the number average molecular weight of the copolymer resin is 22,000, and the weight average molecular weight of the copolymer resin is 51,030.
3. An electrostatographic toner composition in accordance with claim 1 characterized in that as an optional ingredient there is added thereto carrier particles whereby the -toner particles cling to the surface of said carrier particles.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5419179A | 1979-07-02 | 1979-07-02 | |
| US054,191 | 1979-07-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1140785A true CA1140785A (en) | 1983-02-08 |
Family
ID=21989353
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000351553A Expired CA1140785A (en) | 1979-07-02 | 1980-05-09 | Toner composition including carbon black and a copolymer of vinyl chloride and ethyl, propyl or butyl maleate |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0022639B1 (en) |
| JP (1) | JPS5612649A (en) |
| CA (1) | CA1140785A (en) |
| ES (1) | ES493003A0 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60229035A (en) * | 1984-04-27 | 1985-11-14 | Canon Inc | Developing method |
| CN107075029B (en) * | 2015-06-05 | 2020-02-07 | 株式会社Lg化学 | Vinyl chloride-based polymer, method for producing same, and thermoplastic resin composition containing same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5123354B2 (en) * | 1973-01-16 | 1976-07-16 |
-
1980
- 1980-05-09 CA CA000351553A patent/CA1140785A/en not_active Expired
- 1980-06-30 JP JP8905080A patent/JPS5612649A/en active Pending
- 1980-07-01 ES ES493003A patent/ES493003A0/en active Granted
- 1980-07-02 EP EP19800302229 patent/EP0022639B1/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| EP0022639A1 (en) | 1981-01-21 |
| ES8105487A1 (en) | 1981-06-01 |
| ES493003A0 (en) | 1981-06-01 |
| JPS5612649A (en) | 1981-02-07 |
| EP0022639B1 (en) | 1983-05-25 |
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| MKEX | Expiry |