US2891011A - Developer for electrostatic images - Google Patents

Developer for electrostatic images Download PDF

Info

Publication number
US2891011A
US2891011A US630445A US63044556A US2891011A US 2891011 A US2891011 A US 2891011A US 630445 A US630445 A US 630445A US 63044556 A US63044556 A US 63044556A US 2891011 A US2891011 A US 2891011A
Authority
US
United States
Prior art keywords
composition
group
styrene
rosin
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 - Lifetime
Application number
US630445A
Inventor
Michael A Insalaco
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Xerox Corp
Original Assignee
Xerox Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Xerox Corp filed Critical Xerox Corp
Priority to US630445A priority Critical patent/US2891011A/en
Application granted granted Critical
Publication of US2891011A publication Critical patent/US2891011A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/097Plasticisers; Charge controlling agents
    • G03G9/09783Organo-metallic compounds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08702Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08706Polymers of alkenyl-aromatic compounds
    • G03G9/08708Copolymers of styrene
    • G03G9/08711Copolymers of styrene with esters of acrylic or methacrylic acid
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08702Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08726Polymers of unsaturated acids or derivatives thereof
    • G03G9/08728Polymers of esters
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08742Binders for toner particles comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08746Condensation polymers of aldehydes or ketones
    • G03G9/08748Phenoplasts
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08775Natural macromolecular compounds or derivatives thereof
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/09Colouring agents for toner particles
    • G03G9/0902Inorganic compounds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/09Colouring agents for toner particles
    • G03G9/0906Organic dyes
    • G03G9/0912Indigoid; Diaryl and Triaryl methane; Oxyketone dyes

Definitions

  • This invention relates to xerography and more particularly to a composition for developing electrostatic images on xeroradiographic plates.
  • an electrostatic latent image is obtained upon an insulating layer, such as a layer of photoconductive insulating material supported on a conductive backing.
  • a photo conductive insulating layer may be given a uniform elecoped by depositing a finely-divided material on the 1 charged areas of the insulating layer to produce a visible: 1
  • a fine powder may be sprinkled, blown or cascaded acrossthe insulating layer surfaoe after exposure, the powder being preferably charged to apolarity opposite to that to which the insulating layer was initially charged so that electrostatic attraction between the residual image charges in. the layer and the. powder particles will cause deposition and adherence of the latter on the surface of the layer to produce a visible image of the radiographed. object.
  • the xerograph-ic plate or element commonly used in xeroradiography has aphotoconductive layer of insulating material such as amorphous selenium applied to a conductivehacking.
  • the .photoconductive layer is nearly black in color.
  • the developer composition of Rheinfrank and Jones comprises a resin. blend of about 5 to 25% polymerized butyl methacrylate blended with. a polymerized blend of monomers of styrene and styrene homologs of the formula:
  • the invention comprises a developer composition formed by mixing either:
  • R is selected from the group consisting of hydrogen and lower alkyl, the polymerized blend of styrene monomers having a. ring and. ball melting point-of about mhlend of about 5 to about 5.0% of at least ,oneQmet-hr (3)
  • R is selected from the group consisting of hydrogen, methyl, ethyl and propyl.
  • the resin or resin mixture is blended with a zinc salt of S-hydroxyquinoline and with either Prussian Blue or Malachite Green dye.
  • the combination gives a toner of excellent triboelectric properties, great toughness, desirable melting point, no filming characteristics ideally adapted for use under the most adverse conditions in the xerographic process and readily visible against either a black background or a white background.
  • the zinc salt of 8-hydroxyquinoline imparts the necessary triboelectric properties to the indithe appended claims!
  • Example I The invention is carried out in a preferred embodiment by employing as the electroscopic developing powder an electroscopic powder having a fine particle size,
  • the material so obtained has excellent triboelectric properties for use even under the difiicult conditions of xeroradiography as described in the aforesaid Vyverberg patent.
  • a quantity of the resin was stored for two weeks in an oven at 140 F. without deterioration or fusing. Plates developed with this developer composition were easily and readily cleaned without building up annoying and trouble-causing films.
  • composition was also outstanding in uniformity and ease of usablhty both on the xeroradiographic plate and on Example II k mixture was prepared comprising 10 parts of Malach te Green Oxalate, 12 parts of Fluorescent 2500 (a trade name of the New Jersey Zinc Company, for a zinc salt of S-hydroxyquinoline) and 400 parts of a pulverrzed blend of polymerlzed styrenes.
  • the blend of poly- 7 monomer blend of about 5 to about 50% of at least image difliculties.
  • Piccolastic Resin D merized styrenes
  • Piccolastic Resin D is believed to be a mixture of medium high molecular weight styrenes having a ring and ball melting point of 257 F.
  • the mixture was ball milled and 78.5 parts of isopropyl alcohol added and ball milling continued for four hours.
  • the material was dried and screened to yield a powder composition having an average particle size of about 5 microns.
  • the material so obtained has excellent triboelectric properties for use even under the difficult conditions of xerography as described in the aforesaid Vyverberg patent. Plates developed with this composition were easily and readily cleaned without building up annoying and trouble-causing films. Images developed with the composition were characterized by excellent physical properties including absence of solarization and other Example llI
  • a developer composition was prepared as in Example II except that the amount of Fluorescent 2500 was increased from 12 parts to 25 parts.
  • the developer composition so prepared was also characterized by excellent 'triboelectric properties in the xeroradiographic process,
  • the developer composition may be used to prepare :either positive prints or reversal prints as described in the aforesaid Vyverberg patent.
  • images developed with the composition of the instant invention are singularly free from solarization, agglomeration,
  • a xerographic developing powder consisting essentially of between about 2% to about 20% of a zinc salt of S-hydroxyquinoline,
  • composition being a resin fied phenol-formaldehyde resin containing about 5% to selected from the group consisting of (a) a rosin-modi- 45% polyvinyl butyral, the rosinmodified phenol-formaldehyde being prepared using from about 1 to 8 parts rosin for each part of phenol-formaldehyde base and having a ring'and ball melting point of about to 180 C.; (b) a. resin blend of up to 25% polymerized butyl methacrylate blended with a polymerized blend of monomers of styrene and styrene homologs of the formula:
  • R0 C RE where R is selected from the group consisting of hydrogen and lower alkyl, the polymerized blend of styrene a polymerized blend of monomers homologs of the formula:
  • a xerographic developingttbowder consisting essentially of between about 2% to about 20% of a zinc salt of"8hydroxyquinoline, be-
  • R is selected from the group consisting of hydrogen, methyl, ethyl and propyl.
  • a Xerographic developing powder consisting of pigment powder compositions characterized by easy cleanability and melting below 350 F., the composition consisting essentially of particles having an average size between 0.5 and microns and consisting essentially of between about 2% to about 20% of a zinc salt of 8hydroxyquinoline, between about 2% to about 10% of a dye selected from the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a resin selected from the group consisting of (a) a rosin-modified phenol-formaldehyde resin containing about 5% to 45% polyvinyl butyral, the rosin-modified phenol-formaldehyde being prepared using from about 1 to 8 parts rosin for each part of phenol formaldehyde base and having a ring and ball melting point of about 140 to 180 C.; (b) a resin blend of up to 25% polymeiiz'edfbutyl methacrylate -blended with apoly
  • R is selected from the group consisting of hydrogen and lower alkyl, the polymerized blend of styrene monomers having a ring and ball melting point of about 125 C.
  • a xerographic develop ing powder consisting of pigment powder compositions characterized by easy cleanability and melting below 350 F., the composition consisting essentially of particles having an average size between 0.5 and 10 microns and consisting essentially of between about 2% to about 20% of a Xinc salt of S-hydroxyquinoline, between about 2% to about 10% of a dye selected from the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a copolymer resin prepared from a monomer blend of about 5 to about 50% of at "least one methacrylate ester selected consisting of ethyl, propyl and butyl with the balance at least one styrene of the formula:
  • a xerographic developa pigment powder composition characterized by easy cleanability and melting below 350 F. the composition consistingyessentially of particles having an average size between 0.5 and 10 microns and consisting essentially of a rosin-modified phenolformaldehyde resin, between about and about of a dye selected from the group consisting of Prussian Blue and Malchite Green, about 20 to 35 polyvinyl butyral and between about 10% and 20% of a zinc salt of S-hydroxyquinoline, said rosin-modified phenol-formalde' hyde resin prepared using from about 1 to 8 parts rosin to each part of phenol-formaldehyde base and having a ring and ball melting point of about 140 to 180 C.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Developing Agents For Electrophotography (AREA)

Description

United States Patent DEVELOPER FOR ELECTROSTATIC IIVIAGES Michael 'A. 'Insalaco, Rochester, N.Y., assignor to I-laloid Xerox IHCA, a corporation of New York No Drawing. Application December 26, 1956 Serial No. 630,445
11 'Claims. (Cl. 25%-62.1)
This invention relates to xerography and more particularly to a composition for developing electrostatic images on xeroradiographic plates.
In the process of Xeroradiography, an electrostatic latent image is obtained upon an insulating layer, such as a layer of photoconductive insulating material supported on a conductive backing. For example, a photo conductive insulating layer may be given a uniform elecoped by depositing a finely-divided material on the 1 charged areas of the insulating layer to produce a visible: 1
image. Thus, a fine powder may be sprinkled, blown or cascaded acrossthe insulating layer surfaoe after exposure, the powder being preferably charged to apolarity opposite to that to which the insulating layer was initially charged so that electrostatic attraction between the residual image charges in. the layer and the. powder particles will cause deposition and adherence of the latter on the surface of the layer to produce a visible image of the radiographed. object.
The xerograph-ic plate or element commonly used in xeroradiography has aphotoconductive layer of insulating material such as amorphous selenium applied to a conductivehacking. The .photoconductive layer is nearly black in color. t
Very often in xeroradiography it is necessary only toil inspect the powder image on the plate without making. a
permanent record thereof. On the other hand, it is often desired to preserve a permanent record of a particular image and whether the record is to be preserved or not is often not known until after a preliminary viewing of the image. Accordingly, it is desirable that the image be visible bothagainst the relatively black background of the xerographic plate and against the white background of paper, the most commonly used material for keeping permanent records, In addition, a powder, to be. useful in developing xeroradiographic images, must have good storage life even under highly adverse conditions and must not film on the xeroradiographic plate so that the plates may be cleansed thoroughly andquick-ly from all powder for each new use.
. 5% to 45% polyvinyl 2,891,011: Patented June 16, 1959 process places a severe restriction on the triboelectric properties of the powder particles so that it is extremely diificult to obtain materials having the desired charging characteristics.
Recently there have been described in US. 2,753,308 to Richard B. Landrigan and in US. patent application Serial Number 373,431, filed on July 29, 1953., by Rheinfrank and Jones, now [1.3. 2,788,288, developer compositions combining to an exceptional degree the properties of desirable melting point, toughness and resistance to filming.
The developer composition of Landrigan, as described, comprises a rosin-modified phenol formaldehyde resin containing about 5% to about 10% pigment and about butyral, the rosin-modified phenolformaldehyde being prepared using from about 1 to 8 parts rosin for each part of phenol-formaldehyde base and having a ring and ball melting point of about 142 to 149 C.
The developer composition of Rheinfrank and Jones, as described, comprises a resin. blend of about 5 to 25% polymerized butyl methacrylate blended with. a polymerized blend of monomers of styrene and styrene homologs of the formula:
where R is selected from and lower alkyl, liomologs having about 125 C.
To date, however, it has not been possible to use these superior developer compositions in developing Xeroradiographic images because of the difficulty .of imparting the correct triboelectric relationship to the resin particles without adversely affecting the other desirable properties of the resin combination and. in addition preventing solarization, and other difficulties resulting from improper developer properties.
Now, in accordancewith the instant invention; there is provided a composition and a method of manufacture thereof which completely satisfies these diverse .and diffi cult specifications. In general, the invention comprises a developer composition formed by mixing either:
(1) A rosin-modified phenol-formaldehyde resin conthe group consisting of hydrogen the polymerized blend of styrene a ring and ball melting point of ftaining about 5% to 45% polyvinyl butyral, the rosinmodified phenol-formaldehyde being prepared using from about 1 to 8 parts rosin foreach part of phenol-formaldehyde base and having a ring and ball melting point of Finally, the general process of developing, that is,
making visible electrostatic latent images in xeroradiography, is described in .8. 2,759,450 to R. G. Vyverberg. The process involves the formation of a powder cloud of discrete powder particles without opportunity for the use of separate chargingpmeans as an induction ring, corona charging or capillary charging. Accordingly, the sole method of charging .the powder particles in this process is. through triboelecnic contact with each other in the process'of forming thepowder cloud. This 1 about to C.; or
(2) A resin blend of up to 25% polymerized butyl methacryl-ate blended with a polymerized blend of monomers of styrene and styrene homologs of the formula:
Where R is selected from the group consisting of hydrogen and lower alkyl, the polymerized blend of styrene monomers having a. ring and. ball melting point-of about mhlend of about 5 to about 5.0% of at least ,oneQmet-hr (3) A copolymer resin prepared from .a monomer Prussian Blue paper.
propyl and butyl methacrylate and with the balance at least one styrene of the formula:
where R is selected from the group consisting of hydrogen, methyl, ethyl and propyl. 1
In each case the resin or resin mixture is blended with a zinc salt of S-hydroxyquinoline and with either Prussian Blue or Malachite Green dye. The combination gives a toner of excellent triboelectric properties, great toughness, desirable melting point, no filming characteristics ideally adapted for use under the most adverse conditions in the xerographic process and readily visible against either a black background or a white background. It is believed that the zinc salt of 8-hydroxyquinoline imparts the necessary triboelectric properties to the indithe appended claims! Example I The invention is carried out in a preferred embodiment by employing as the electroscopic developing powder an electroscopic powder having a fine particle size,
for example of approximately 3 to 7 microns, and being a mixture approximately in parts by weight of:
= (a trade name of Union Carbide & Carbon Corp.
for a polyvinyl butyral resin) 25 Fluorescent 2500 (a trade name of the New Jersey Zinc Company for a zinc salt of S-hydroxyquinolone) 14 /3 The Amberol M-93 is added to a batch mixer and heated to the point of plasticization; then the Vinylite .XYI -I L is added and the mixing continued for about two minutes. Finally, the Prussian Blue is added and themixing continued until thorough dispersion of the components is obtainedgenerally in about 5 minutes. Overheating must be avoided, particularly after the Prussian Blue is added. The material is then removed from the mixer and further blended on a two roll mill. 4
The Fluorescent 2500 is added on the mill where the i material is blended for about one-half hour.
The mixture is then removed from the mill, cooled, crushed and pulverized to obtain the desired particle size.
The material so obtained has excellent triboelectric properties for use even under the difiicult conditions of xeroradiography as described in the aforesaid Vyverberg patent. A quantity of the resin was stored for two weeks in an oven at 140 F. without deterioration or fusing. Plates developed with this developer composition were easily and readily cleaned without building up annoying and trouble-causing films. The composition was also outstanding in uniformity and ease of usablhty both on the xeroradiographic plate and on Example II k mixture was prepared comprising 10 parts of Malach te Green Oxalate, 12 parts of Fluorescent 2500 (a trade name of the New Jersey Zinc Company, for a zinc salt of S-hydroxyquinoline) and 400 parts of a pulverrzed blend of polymerlzed styrenes. The blend of poly- 7 monomer blend of about 5 to about 50% of at least image difliculties.
merized styrenes is available under the trade name Piccolastic Resin D and is believed to be a mixture of medium high molecular weight styrenes having a ring and ball melting point of 257 F.
The mixture was ball milled and 78.5 parts of isopropyl alcohol added and ball milling continued for four hours. The material was dried and screened to yield a powder composition having an average particle size of about 5 microns.
The material so obtained has excellent triboelectric properties for use even under the difficult conditions of xerography as described in the aforesaid Vyverberg patent. Plates developed with this composition were easily and readily cleaned without building up annoying and trouble-causing films. Images developed with the composition were characterized by excellent physical properties including absence of solarization and other Example llI A developer composition was prepared as in Example II except that the amount of Fluorescent 2500 was increased from 12 parts to 25 parts. The developer composition so prepared was also characterized by excellent 'triboelectric properties in the xeroradiographic process,
high imagequality, absence of solarization, no filming and excellent cleanability from the xerographic plate.
Example IV Wasjincreased to 25 parts. The developer composition so prepared was characterized by excellent triboelectric properties in the xeroradiographic process, high quality of the developed image, absence of solarization and exceptional ease of cleanability and absence of annoying filming properties.
The developer composition may be used to prepare :either positive prints or reversal prints as described in the aforesaid Vyverberg patent. In addition, images developed with the composition of the instant invention are singularly free from solarization, agglomeration,
. graininess and similar defects.
While specific examples may be described, variations within the scope of the claims are possible and are contemplated. There is no intention, therefore, to limit the invention to the exact details shown and described.
I claim:
1. As a composition of matter, a xerographic developing powder consisting essentially of between about 2% to about 20% of a zinc salt of S-hydroxyquinoline,
between about 2% to about 10% of a dye selected from 1 the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a resin fied phenol-formaldehyde resin containing about 5% to selected from the group consisting of (a) a rosin-modi- 45% polyvinyl butyral, the rosinmodified phenol-formaldehyde being prepared using from about 1 to 8 parts rosin for each part of phenol-formaldehyde base and having a ring'and ball melting point of about to 180 C.; (b) a. resin blend of up to 25% polymerized butyl methacrylate blended with a polymerized blend of monomers of styrene and styrene homologs of the formula:
R0=C RE where R is selected from the group consisting of hydrogen and lower alkyl, the polymerized blend of styrene a polymerized blend of monomers homologs of the formula:
"'5 one 'methacrylate ester'selected from the :grou consisting of ethyl, propyl and butyl methalcrylateandwith'thefbalance at least One'styIene of'the formula:
where R is selected from the.group consisting of-hydro- 1 gen, methyl, ethyl "and .propyl.
for each 1 partof phenol foirnaldehyde base and having a ring and ballmelting pointof about 140 to 180C.
3. As a 'compositionof matter, a xerographic developingttbowder consisting essentially of between about 2% to about 20% of a zinc salt of"8hydroxyquinoline, be-
tween about 2% to about l'% 'of adye selected-from the group consisting of Prussian Blue and Malachite Green and the balance df=said composition being aresin blend of up to 25% poiyrnerized 'hatylanetnacrylate blended with of styrene and "styrene where R is selected from the group consisting of hydrogen and lower alkyl, the polymerized blend of styrene monomers having a ring and ball melting point of about 125 C.
4. As a composition of matter, a xerographic developing powder consisting essentially of between about 2% to about 20% of a zinc salt of 8-hydroxyquinoline, between about 2% to about 10% of a dye selected from the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a copolymer resin prepared from a monomer blend of about 5 to about 50% of at least one methacrylate ester selected from the group consisting of ethyl, propyl and butyl methacrylate and with the balance at least one styrene of the formula:
where R is selected from the group consisting of hydrogen, methyl, ethyl and propyl.
5. As a composition of matter, a Xerographic developing powder consisting of pigment powder compositions characterized by easy cleanability and melting below 350 F., the composition consisting essentially of particles having an average size between 0.5 and microns and consisting essentially of between about 2% to about 20% of a zinc salt of 8hydroxyquinoline, between about 2% to about 10% of a dye selected from the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a resin selected from the group consisting of (a) a rosin-modified phenol-formaldehyde resin containing about 5% to 45% polyvinyl butyral, the rosin-modified phenol-formaldehyde being prepared using from about 1 to 8 parts rosin for each part of phenol formaldehyde base and having a ring and ball melting point of about 140 to 180 C.; (b) a resin blend of up to 25% polymeiiz'edfbutyl methacrylate -blended with apolymerizfedblend of monomersof styrene andstyrene homologs of "the formula:
R'C="CRH where R is' selected from the group consisting of hydrogen and lower alkyl, the polymerized "blenilofstyrene monomers having a ring and ball melting p'oint'o'f about C.; and (c') a copolymer resinprepared from a monomer blend of aboutS to about 50% ofat'least-one methacrylate ester selected from the group consisting of ethyl, propyl and butyl' metlracrylate and w'iththebalance at least one styrene of the formula:
where'R -is selected'from the {group consis ting of "hydro- .gen methyl, ethyl and. propyl.
6. As a'compositiomof'matter, axerographic developing, powder consisting of pigment powder compositions characterized 'by easy cleanability and melting below 350 F., the composition consisting essentially of particleshaving an average sizebetween0.5farid10"microns and consistingessentially-of between about2% to about 20% of a zinc salt of'8 hydroxyqui1ioli'ne, between about 2% to about 10% of a dye selected from the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a rosin-modified phenol-formaldehyde resin containing about 5% to 45% polyvinyl butyral, the rosin-modified phenol-formaldehyde being prepared using from about 1 to 8 parts rosin for each part of phenol-formaldehyde base and having a ring and ball melting point of about to C.
7. As a composition of matter, a Xerographic developing powder consisting of pigment powder compositions characterized by easy cleanability and melting below 350 F., the composition consisting essentially of particles having an average size between 0.5 and 10 microns and consisting essentially of between about 2% to about 20% of a zinc salt of 8-hydroxyquino1ine, between about 2% to about 10% of a dye selected from the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a resin blend of up to 25% polymerized butyl methacrylate blended with a polymerized blend of monomers of styrene and styrene homologs of the formula:
where R is selected from the group consisting of hydrogen and lower alkyl, the polymerized blend of styrene monomers having a ring and ball melting point of about 125 C.
8. As a composition of matter, a xerographic develop ing powder consisting of pigment powder compositions characterized by easy cleanability and melting below 350 F., the composition consisting essentially of particles having an average size between 0.5 and 10 microns and consisting essentially of between about 2% to about 20% of a Xinc salt of S-hydroxyquinoline, between about 2% to about 10% of a dye selected from the group consisting of Prussian Blue and Malachite Green and the balance of said composition being a copolymer resin prepared from a monomer blend of about 5 to about 50% of at "least one methacrylate ester selected consisting of ethyl, propyl and butyl with the balance at least one styrene of the formula:
ing powder consisting of from the group methacrylate and where R is selected from the group consisting of hydrogen, methyl, ethyland propyl.
9. As a composition of matter, a xerographic developa pigment powder composition characterized by easy cleanability and melting below 350 F., the composition consistingyessentially of particles having an average size between 0.5 and 10 microns and consisting essentially of a rosin-modified phenolformaldehyde resin, between about and about of a dye selected from the group consisting of Prussian Blue and Malchite Green, about 20 to 35 polyvinyl butyral and between about 10% and 20% of a zinc salt of S-hydroxyquinoline, said rosin-modified phenol-formalde' hyde resin prepared using from about 1 to 8 parts rosin to each part of phenol-formaldehyde base and having a ring and ball melting point of about 140 to 180 C.
10. As a composition of matter, a xerographic developing powder consisting of pigment powder composi tions characterized by easy cleanability and melting below 350 F., the composition vconsisting essentially of particles having an average size between 0.5 and 10 microns and consisting essentially of a resin body prepared by copolymerizing a mixture of about 10 to 35% about 5% and about 10% butyl methacrylate and the remainder styrene, between of a dye selected from the group consisting of PrussianQBIue and Malachite Green and between about 10% and 20% of a zinc salt of 8- hydroxyquinoline.
11. As a composition of matter, a xerographic developing powder consisting of pigment powder compositions characterized by easy cleanability and melting below 350 F., the composition consisting essentially of particles having an average particle size between 0.5 and 10 microns and consisting essentially of a polymerized blend of monomers of styrene and styrene homologs of the formula:
1 Malachite Green and between about 10% and about 20% of a zinc salt of 8-hydroxyquinoline.
References Cited in the file of this patent UNITED STATES PATENTS

Claims (1)

1. AS A COMPOSITION OF MATTER, A XEROGRAPHIC DEVELOPING POWDER CONSISTING ESSENTIALLY OF BETWEEN ABOUT 2% TO ABOUT 20% OF A ZINC SALT OF 8-HYDROXYQUINOLINE, BETWEEN ABOUT 2% TO ABOUT 10% OF A DYE SELECTED FROM THE GROUP CONSISTING OF PRUSSIAN BLUE AND MALACHITE GREEN AND THE BALANCE OF SAID COMPOSITION BEING A RESIN SELECTED FROM THE GROUP CONSISTING OF (A) A ROSIN-MODIFIED PHENOL-FORMALDEHYDE RESIN CONTAINING ABOUT 5% TO 45% POLYVINYL BUTYRAL, THE ROSIN-MODIFIED PHENOL-FORMALDEHYDE BEING PREPARED USING FROM ABOUT 1 TO 8 PARTS ROSIN FOR EACH PART OF PHENOL-FORMALDEHYDE BASE AND HAVING A RING AND BALL MELTING POINT OF ABOUT 140 TO 180* C.; (B) A RESIN BLEND OF UP TO 25% POLYMERIZED BUTYL METHACRYLATE BLENDED WITH A POLYMERIZED BLEND OF MONOMERS OF STYRENE AND STYRENE HOMOLOGS OF THE FORMULA:
US630445A 1956-12-26 1956-12-26 Developer for electrostatic images Expired - Lifetime US2891011A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US630445A US2891011A (en) 1956-12-26 1956-12-26 Developer for electrostatic images

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US630445A US2891011A (en) 1956-12-26 1956-12-26 Developer for electrostatic images

Publications (1)

Publication Number Publication Date
US2891011A true US2891011A (en) 1959-06-16

Family

ID=24527198

Family Applications (1)

Application Number Title Priority Date Filing Date
US630445A Expired - Lifetime US2891011A (en) 1956-12-26 1956-12-26 Developer for electrostatic images

Country Status (1)

Country Link
US (1) US2891011A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3078231A (en) * 1959-05-13 1963-02-19 Commw Of Australia Controlled developer for use in electro-photography and electro-radiography
US3079342A (en) * 1960-02-12 1963-02-26 Xerox Corp Electrostatic developer composition and method therefor
US3280741A (en) * 1958-12-31 1966-10-25 Burroughs Corp Electrostatic recording
US3300498A (en) * 1962-05-08 1967-01-24 Gershon Herman 8-hydroxyquinoline metal chelates
US3419411A (en) * 1963-09-06 1968-12-31 Australia Res Lab Method for the transfer of developed electrostatic images using a lattice forming substance
US3874896A (en) * 1968-07-11 1975-04-01 Ricoh Kk Reversible developer for electrostatic latent imaging method
EP0058355A1 (en) * 1981-02-17 1982-08-25 International Business Machines Corporation Xerographic toner composition
US4518673A (en) * 1982-04-28 1985-05-21 Hitachi Metals, Ltd. Electrophotographic developer
US5073469A (en) * 1990-08-09 1991-12-17 Lexmark International, Inc. Toner compositions

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2753308A (en) * 1952-12-22 1956-07-03 Haloid Co Xerography developer composition
US2788288A (en) * 1953-07-29 1957-04-09 Haloid Co Process and composition for developing an electrostatic image

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2753308A (en) * 1952-12-22 1956-07-03 Haloid Co Xerography developer composition
US2788288A (en) * 1953-07-29 1957-04-09 Haloid Co Process and composition for developing an electrostatic image

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3280741A (en) * 1958-12-31 1966-10-25 Burroughs Corp Electrostatic recording
US3078231A (en) * 1959-05-13 1963-02-19 Commw Of Australia Controlled developer for use in electro-photography and electro-radiography
US3079342A (en) * 1960-02-12 1963-02-26 Xerox Corp Electrostatic developer composition and method therefor
US3300498A (en) * 1962-05-08 1967-01-24 Gershon Herman 8-hydroxyquinoline metal chelates
US3419411A (en) * 1963-09-06 1968-12-31 Australia Res Lab Method for the transfer of developed electrostatic images using a lattice forming substance
US3874896A (en) * 1968-07-11 1975-04-01 Ricoh Kk Reversible developer for electrostatic latent imaging method
EP0058355A1 (en) * 1981-02-17 1982-08-25 International Business Machines Corporation Xerographic toner composition
US4518673A (en) * 1982-04-28 1985-05-21 Hitachi Metals, Ltd. Electrophotographic developer
US5073469A (en) * 1990-08-09 1991-12-17 Lexmark International, Inc. Toner compositions

Similar Documents

Publication Publication Date Title
JP3421751B2 (en) Toner for developing electrostatic images
US2892794A (en) Electrostatic developer and toner
JPS5950060B2 (en) Electrophotographic toner composition
JPS63280262A (en) Toner for developing electrostatic latent image
US2891011A (en) Developer for electrostatic images
US6455215B1 (en) Magenta toner for electrophotography, magenta developer for electrophotography, and image forming method using the same
US2753308A (en) Xerography developer composition
US5110704A (en) Toner for developing statically charged images and process for preparation thereof
JPH0772809B2 (en) Thermal fixing toner for high speed copying
US4645729A (en) Method for preventing offset in electrophotography
JPH0154694B2 (en)
JPH0566583B2 (en)
JP3225218B2 (en) Non-magnetic toner
JPH0232622B2 (en)
JPH0797241B2 (en) Toner for electrophotography
JPH058430B2 (en)
US5236799A (en) Electrophotographic toner composition
JPS60179748A (en) Electrostatic charge image developing toner
JPH04255865A (en) Dry toner and production thereof
JP2769870B2 (en) Manufacturing method of toner
JPS58106552A (en) Heat fixable dry type developing toner
JPH03209265A (en) Nonmagnetic toner for developing electrostatic charge image
JP3108836B2 (en) Color developer
CA2007197A1 (en) Toner composition comprising rosin modified styrene acrylic resin
JPS60254157A (en) Dry toner for electrophotography