US3761413A - Xerographic toner composition - Google Patents
Xerographic toner composition Download PDFInfo
- Publication number
- US3761413A US3761413A US00194697A US3761413DA US3761413A US 3761413 A US3761413 A US 3761413A US 00194697 A US00194697 A US 00194697A US 3761413D A US3761413D A US 3761413DA US 3761413 A US3761413 A US 3761413A
- Authority
- US
- United States
- Prior art keywords
- weight
- toner
- toner composition
- resin particles
- colorant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title abstract description 22
- 239000002245 particle Substances 0.000 abstract description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 12
- 239000003086 colorant Substances 0.000 abstract description 10
- 229920001577 copolymer Polymers 0.000 abstract description 9
- 239000011347 resin Substances 0.000 abstract description 9
- 229920005989 resin Polymers 0.000 abstract description 9
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 abstract description 8
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- -1 polytetrafluoroethylene Polymers 0.000 description 6
- 238000005054 agglomeration Methods 0.000 description 5
- 230000002776 aggregation Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 230000007257 malfunction Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 229920001897 terpolymer Polymers 0.000 description 3
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000013021 overheating Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 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
- 229920000742 Cotton Polymers 0.000 description 1
- 241000183290 Scleropages leichardti Species 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000012612 commercial material Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance 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
- G03G9/08706—Polymers of alkenyl-aromatic compounds
- G03G9/08708—Copolymers of styrene
- G03G9/08711—Copolymers of styrene with esters of acrylic or methacrylic acid
-
- 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
- G03G9/08706—Polymers of alkenyl-aromatic compounds
- G03G9/08708—Copolymers of styrene
-
- 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
- G03G9/0872—Polyvinylhalogenides containing fluorine
-
- 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
- G03G9/08728—Polymers of esters
Definitions
- a xerographic toner composition consisting essentially of finely divided resin particles produced by copolymeriz ing a mixture of methylmethacrylate, styrene and n-butylmethacrylate having a colorant intimately dispersed in the resin particles and a minor amount in the range about 0.2 to 1.0 percent by weight based on the weight of the resin particles of a polymer or copolymer of fluorocarbons containing two or three carbon atoms per molecule.
- the photoconductive surface is commonly the exterior surface of a drum which is driven at uniform speed so that each point on the drum surface moves through the entire machine cycle over and over.
- the cleaning step of the cycle is commonly carried out by moving a fibrous web such as cotton cloth across a portion of the drum surface in a direction opposite to that of the drum rotation.
- the toner composition of the present invention is a mixture of resinous particles having a colorant uniformly dispersed in the particle and a small amount of finely divided polytetrafluoroethylene or of finely divided copolymer of tetrafluoroethylene and hexafluoropropylene.
- the resin is prepared by copolymerizing a mixture of two parts by weight of n-butylrnethacrylate, 1.8 to 2.2 parts by weight of styrene and 0.8 to 1.2 parts by weight of methylmethacrylate.
- the resin is predominantly a terpolymer having a molecular weight in the range about 50,000 to 75,000 and a melt index range of 8 to 20.
- Molecular weight range and melt index range are controlled by adjusting the amount of polymerization initiator and the temperature employed in the polymerization step.
- the resins are free flowing at 60 to 70 C., begin to exhibit tack at about to C. and melt at to 105 C.
- the contents of the flask were blanketed with nitrogen, mechanically stirred and held at 90 C. for four hours and at C. for one hour. When the contents had been at 90 C. for 1.5 hours, 0.15 g. of powdered calcium carbonate was added to the contents of the flask.
- the contents of the flask were cooled, passed through a filter and the polymer filter cake was washed with water and then dried in a vacuum oven at 104 F.
- the polymer product weighed 201.2 g. and had a melt index 8.8 (ASTM D-123865T). The polymer was subjected to the Kofler Hot Bench Test and showed free flow 62 C., tack 90 C., melt 105 C.
- the polymer product was then melted and 45 grams of finely divided carbon black (Regal 400-R supplied by Cabot Corp.) were intimately mixed with the molten polymer. The resulting mixture was cooled until it solidified and then jet pulverized to produce particles having an average maximum dimnesion in the range 10 to 20 microns.
- finely divided carbon black (Regal 400-R supplied by Cabot Corp.)
- Finely divided copolymer of approximately equimolar amounts of tetrafluoroethylene and hexafiuoropropylene having an estimated average maximum dimension about 0.7 micron was mixed with the polymer-carbon black particles in amount to produce a mixture having a polyfluorocarbon content of 0.5% by weight.
- the resulting mixture was then charged to a Twinshell blender which was run for a 15-minute blending period to produce the finished toner composition.
- the polyfluorocarbon content of the toner composition was varied over a considerable range. At least 0.2% by weight of polytetrafiuoroethylene or copolymer of tetrafluoroethylenehexafiuoropropylene is required to make significant improvement, increasing polyfluorocarbon content above 1% by weight does not result in increased improvement and about 0.5 by weight appears optimum.
- Polytetrafluoroethylene is commercially available in fine powder form. The powder particles are small, well below 15 microns. The commercial material, e.g., Teflon (duPont) is satisfactory for use in the toner composition.
- Copolymers of tetrafluoroethylene and hexafluoropylene are also available commercially. The copolymer of approximately equal molar amounts of tetrafiuoroethylene and hexafiuoropropylene employed in the above example is sold by Liquid Nitrogen Processing Corp. as TL-120FEP in the form of a powder having an average particle size about 0.7 micron; it is a preferred polyfluorocarbon for use in the toner compositions of the invention. Polyfluorocarbon preparation and properties are shown in Encyclopedia of Chemical Technology, Kirk-Othrner, Interscience Encyclopedia, Inc., N.Y., 1953, at vol. 11, pg. 689 et seq.
- Carbon black is the preferred colorant but other colorants in the form of pigments or dyes may be employed. Such other colorants are well known in the art as illustrated, for example, in U.S. Pat. 3,577,345.
- the toner of the present invention is unusually resistant to thermal agglomeration and exhibits remark ably strong adherence to the image surface.
- Resistance to agglomeration was measured by placing toner samples in aluminum dishes and exposing them to varyin oven temperatures for 18 hour periods.
- Samples of the toner produced pursuant to the above example showed essentially no agglomeration at 130 F. while a widely used commercial toner showed 50% agglomeration at 125 F. and was fused to a cake at 130 F.
- the toner of the present invention can be stored in any ordinary storage facility and in any climate without experiencing agglomeration loss.
- the toner of the present invention exhibits superior fix or adhesion to the image surface after fusion. This property of a toner is tested by applying pieces of transparent adhesive tape to selected areas of the image surface, peeling the tape from the image surface and then applying the tape to a blank white piece of paper. Colorant adhering to the adhesive tape is readily detected against the blank white surface.
- the fix of the toner of the present invention was compared with that of commercial toners using Norton Bear-Rite Mending Tape No. 335 as the transparent tape. Identical images were produced using the toner of the present invention and three commercial toners. All images were at a nominal 1.0 optical density and were produced in a Xerox 660 type machine.
- Transparent tape was applied and removed from the upper left, center and lower right areas of each image and the removed tape strips were placed against blank white paper for comparison. No colorant adhered to the tape strips when the toner of the present invention was employed. Colorant adhered to the tape strips with all three of the compared commercial toners in varying amounts ranging from scattered spots to heavy deposits which defined some of the text of the image.
- a xerographic toner composition consisting essentially of:
- a colorant selected from the group consisting of dyes and pigments in amount sufiicient to color the resin.
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
A XEROGRAPHIC TONER COMPOSITION CONSISTING ESSENTIALLY OF FINELY DIVIDED RESIN PARTICLES PRODUCED BY COPOLYMERIZING A MIXTURE OF METHYLMETHACRYLATE, STYRENE AND N-BUTYLMETHACRYLATE HAVING A COLORANT INTIMATELY DISPERSED IN THE RESIN PARTICLES AND A MINOR AMOUNT IN THE RANGE ABOUT 0.2 TO 1.0 PERCENT BY WEIGHT BASED ON THE WEIGHT OF THE RESIN PARTICLES OF A POLYMR OR COPOLYMER OF FLUOROCARBONS CONTAINING TWO OR THREE CARBON ATOMS PER MOLECULE.
Description
United States Patent 3,761,413 XEROGRAPHIC TONER COMPOSITION, Lauren L. Hulse, Saratoga, Calif., assignor to Memorex Corporation No Drawing. Filed Nov. 1, 1971, Ser. No. 194,697 Int. Cl. G03g 9/02 US. Cl. 252-621 3 Claims ABSTRACT OF THE DISCLOSURE A xerographic toner composition consisting essentially of finely divided resin particles produced by copolymeriz ing a mixture of methylmethacrylate, styrene and n-butylmethacrylate having a colorant intimately dispersed in the resin particles and a minor amount in the range about 0.2 to 1.0 percent by weight based on the weight of the resin particles of a polymer or copolymer of fluorocarbons containing two or three carbon atoms per molecule.
BACKGROUND OF THE INVENTION surface and fusing the toner particles on that surface,
cleaning the photoconductive surface to remove residual toner particles; the cycle is then repeated.
The photoconductive surface is commonly the exterior surface of a drum which is driven at uniform speed so that each point on the drum surface moves through the entire machine cycle over and over. The cleaning step of the cycle is commonly carried out by moving a fibrous web such as cotton cloth across a portion of the drum surface in a direction opposite to that of the drum rotation.
In connection with a study of the causes of machine malfunction, an ammeter was connected in series with the main drive motor for the drum, and the ammeter readings were recorded during continuous operation of the machine. It was observed that periodic rapid increases in the current pull of the drive motor occurred during operation. For example, a drive motor having a normal current pull of 0.50 amperes would show sudden increases in current pull of as much as 0.06 amperes. A study of the increases in current pull as related to machine operation indicated that current pull increases up to about 0.03 amperes does not appear to correlate with any malfunction of the machine but that where current pull increases are above 0.03 amperes and especially when they are above 0.04 amperes, the image surface paper becomes overheated in the fusion step of the cycle, and fires commonly occur at that point. It is believed that sudden increases in the current pull indicates suddenly increased frictional resistance to drum rotation experienced at the cleaning step of the cycle and that this is accompanied by decreased drum speed, increased residence of the image surface in the fuser, overheating of the paper and frequently fires in the fuser.
It has been found that when the toner composition described herein is used, sudden increases in current pull of as much as 0.04 amperes are rare and that prolonged operation of the machine is possible without malfunctions due to overheating.
3,761,413 Patented Sept. 25, 1973 DETAILED DESCRIPTION OF THE INVENTION The toner composition of the present invention is a mixture of resinous particles having a colorant uniformly dispersed in the particle and a small amount of finely divided polytetrafluoroethylene or of finely divided copolymer of tetrafluoroethylene and hexafluoropropylene.
The resin is prepared by copolymerizing a mixture of two parts by weight of n-butylrnethacrylate, 1.8 to 2.2 parts by weight of styrene and 0.8 to 1.2 parts by weight of methylmethacrylate. The resin is predominantly a terpolymer having a molecular weight in the range about 50,000 to 75,000 and a melt index range of 8 to 20. Molecular weight range and melt index range are controlled by adjusting the amount of polymerization initiator and the temperature employed in the polymerization step.
As determined by the Kofler Hot Bench Test, the resins are free flowing at 60 to 70 C., begin to exhibit tack at about to C. and melt at to 105 C.
A representative preparation of the toner of the present invention is described in the following example.
Example 504 grams of deionized Water, 33.8 grams of water solution of sodium phosphate having a 7.39% by weight content of sodium phosphate and 17.1 grams of a water solution of calcium chloride having a 20.3% by weight content of calcium chloride were placed in a 3L round bottom flask equipped with a mechanical stirrer, a thermometer, a condenser and an inlet for nitrogen gas. Nitrogen was bubbled through the mixture in the flask while heating it to 90 C. A mixture of 8.13 grams benzoyl peroxide, 0.04 gram of dioctyl sodium succinate (aerosol OT sold by American Cyanamid Co.), 120 grams styrene, 120 grams n-butylmethacrylate and 60 grams of methylmethacrylate was introduced into the flask. The contents of the flask were blanketed with nitrogen, mechanically stirred and held at 90 C. for four hours and at C. for one hour. When the contents had been at 90 C. for 1.5 hours, 0.15 g. of powdered calcium carbonate was added to the contents of the flask. The contents of the flask were cooled, passed through a filter and the polymer filter cake was washed with water and then dried in a vacuum oven at 104 F.
The polymer product weighed 201.2 g. and had a melt index 8.8 (ASTM D-123865T). The polymer was subjected to the Kofler Hot Bench Test and showed free flow 62 C., tack 90 C., melt 105 C.
The polymer product was then melted and 45 grams of finely divided carbon black (Regal 400-R supplied by Cabot Corp.) were intimately mixed with the molten polymer. The resulting mixture was cooled until it solidified and then jet pulverized to produce particles having an average maximum dimnesion in the range 10 to 20 microns.
Finely divided copolymer of approximately equimolar amounts of tetrafluoroethylene and hexafiuoropropylene having an estimated average maximum dimension about 0.7 micron was mixed with the polymer-carbon black particles in amount to produce a mixture having a polyfluorocarbon content of 0.5% by weight. The resulting mixture was then charged to a Twinshell blender which was run for a 15-minute blending period to produce the finished toner composition.
A number of preparations of toner were made generally following the procedure of the above example. The proportions of the monomers charged to the polymerization reaction were varied and the results indicated that the proportions must be held within the ranges two parts by weight n-butuylmethacrylate, 1.8 to 2.2 parts by weight styrene and 0.8 to 1.2 parts by weight methylmethacrylate if uniform satisfactory resin properties were to be obtained.
The polyfluorocarbon content of the toner composition was varied over a considerable range. At least 0.2% by weight of polytetrafiuoroethylene or copolymer of tetrafluoroethylenehexafiuoropropylene is required to make significant improvement, increasing polyfluorocarbon content above 1% by weight does not result in increased improvement and about 0.5 by weight appears optimum.
Polytetrafluoroethylene is commercially available in fine powder form. The powder particles are small, well below 15 microns. The commercial material, e.g., Teflon (duPont) is satisfactory for use in the toner composition. Copolymers of tetrafluoroethylene and hexafluoropylene are also available commercially. The copolymer of approximately equal molar amounts of tetrafiuoroethylene and hexafiuoropropylene employed in the above example is sold by Liquid Nitrogen Processing Corp. as TL-120FEP in the form of a powder having an average particle size about 0.7 micron; it is a preferred polyfluorocarbon for use in the toner compositions of the invention. Polyfluorocarbon preparation and properties are shown in Encyclopedia of Chemical Technology, Kirk-Othrner, Interscience Encyclopedia, Inc., N.Y., 1953, at vol. 11, pg. 689 et seq.
Carbon black is the preferred colorant but other colorants in the form of pigments or dyes may be employed. Such other colorants are well known in the art as illustrated, for example, in U.S. Pat. 3,577,345.
In addition to improving the reliability of machine operation, the toner of the present invention is unusually resistant to thermal agglomeration and exhibits remark ably strong adherence to the image surface.
Resistance to agglomeration was measured by placing toner samples in aluminum dishes and exposing them to varyin oven temperatures for 18 hour periods.
Samples of the toner produced pursuant to the above example showed essentially no agglomeration at 130 F. while a widely used commercial toner showed 50% agglomeration at 125 F. and was fused to a cake at 130 F.
The toner of the present invention can be stored in any ordinary storage facility and in any climate without experiencing agglomeration loss.
The toner of the present invention exhibits superior fix or adhesion to the image surface after fusion. This property of a toner is tested by applying pieces of transparent adhesive tape to selected areas of the image surface, peeling the tape from the image surface and then applying the tape to a blank white piece of paper. Colorant adhering to the adhesive tape is readily detected against the blank white surface. The fix of the toner of the present invention was compared with that of commercial toners using Norton Bear-Rite Mending Tape No. 335 as the transparent tape. Identical images were produced using the toner of the present invention and three commercial toners. All images were at a nominal 1.0 optical density and were produced in a Xerox 660 type machine. Transparent tape was applied and removed from the upper left, center and lower right areas of each image and the removed tape strips were placed against blank white paper for comparison. No colorant adhered to the tape strips when the toner of the present invention was employed. Colorant adhered to the tape strips with all three of the compared commercial toners in varying amounts ranging from scattered spots to heavy deposits which defined some of the text of the image.
I claim:
1. A xerographic toner composition consisting essentially of:
(a) a major proportion of 10 to 20 micron particles of a polymer having a molecular weight in the range 50,000 to 75,000, said polymer being a terpolymer of 2 parts by weight n-butylmethacrylate, 1.8 to 2.2 parts by weight styrene and 0.8 to 1.2 parts by weight methylmethacrylate;
(b) from 0.2% to 1% by weight based on the terpolymer of a finely divided fluorocarbon selected from the group consisting of polytetrafluoroethylene, polyhexafluoropropylene and copolymers of tetrafiuoroethylene and hexafluoropropylene; and
(c) a colorant selected from the group consisting of dyes and pigments in amount sufiicient to color the resin.
2. A xerographic toner composition as defined in claim 1 in which the fluorocarbon polymer is polytetrafiuoroethylene.
3. A xerographic toner composition as defined in claim 1 in which the fluorocarbon polymer is a copolymer of tetrafiuoroethylene and hexofluoropropylene.
References Cited UNITED STATES PATENTS 3,502,582 3/1970 Clemens et al. 252-62.1
NORMAN G. TORCHIN, Primary Examiner J. P. BRAMMER, Assistant Examiner U.S. Cl. X.R. 1l717.5; 260-900
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19469771A | 1971-11-01 | 1971-11-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3761413A true US3761413A (en) | 1973-09-25 |
Family
ID=22718580
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00194697A Expired - Lifetime US3761413A (en) | 1971-11-01 | 1971-11-01 | Xerographic toner composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3761413A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3922381A (en) * | 1974-06-14 | 1975-11-25 | Addressorgrap Multigraph Corp | Chemically treated carrier particles for use in electrophotographic process |
| FR2386847A1 (en) * | 1977-04-07 | 1978-11-03 | Mita Industrial Co Ltd | DEVELOPER FOR ELECTROSTATIC IMAGES |
| EP0051830A1 (en) * | 1980-11-07 | 1982-05-19 | E.I. Du Pont De Nemours And Company | Dry nonelectroscopic toners and process for toning tacky image surfaces |
| US4371599A (en) * | 1975-12-15 | 1983-02-01 | Hoechst Aktiengesellschaft | Process for the preparation of printing forms and/or metallized images |
| US4666813A (en) * | 1985-01-08 | 1987-05-19 | Canon Kabushiki Kaisha | Developer for developing electrostatic latent images contains vinylidene fluoride polymer |
| US5244766A (en) * | 1991-12-03 | 1993-09-14 | Xerox Corporation | Halogenated resins for liquid developers |
-
1971
- 1971-11-01 US US00194697A patent/US3761413A/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3922381A (en) * | 1974-06-14 | 1975-11-25 | Addressorgrap Multigraph Corp | Chemically treated carrier particles for use in electrophotographic process |
| US4371599A (en) * | 1975-12-15 | 1983-02-01 | Hoechst Aktiengesellschaft | Process for the preparation of printing forms and/or metallized images |
| FR2386847A1 (en) * | 1977-04-07 | 1978-11-03 | Mita Industrial Co Ltd | DEVELOPER FOR ELECTROSTATIC IMAGES |
| EP0051830A1 (en) * | 1980-11-07 | 1982-05-19 | E.I. Du Pont De Nemours And Company | Dry nonelectroscopic toners and process for toning tacky image surfaces |
| US4666813A (en) * | 1985-01-08 | 1987-05-19 | Canon Kabushiki Kaisha | Developer for developing electrostatic latent images contains vinylidene fluoride polymer |
| US5244766A (en) * | 1991-12-03 | 1993-09-14 | Xerox Corporation | Halogenated resins for liquid developers |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: MEMOREX DIC CORPORATION, 1200 MEMOREX DR., SANTA C Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:MEMOREX CORPORATION;REEL/FRAME:003833/0592 Effective date: 19810219 |