US3058914A - Non-inflammable liquid developers for electrostatic images - Google Patents

Non-inflammable liquid developers for electrostatic images Download PDF

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Publication number
US3058914A
US3058914A US762912A US76291258A US3058914A US 3058914 A US3058914 A US 3058914A US 762912 A US762912 A US 762912A US 76291258 A US76291258 A US 76291258A US 3058914 A US3058914 A US 3058914A
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liquid
particles
developer
resins
electrostatic images
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US762912A
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Kenneth A Metcalfe
Robert J Wright
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Commonwealth of Australia
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Commonwealth of Australia
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Priority claimed from AU31770/57A external-priority patent/AU236835B2/en
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    • 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
    • G03G9/12—Developers with toner particles in liquid developer mixtures
    • G03G9/125—Developers with toner particles in liquid developer mixtures characterised by the liquid

Definitions

  • This invention relates to non-inflammable liquid developers for electrostatic images.
  • Liquids having the required characteristics are generally of an inflammatory nature and while the hazard of using them is extremely small or non-existent under suitable operating conditions, an object of this invention is to provide an improvement with respect to this type of developer which will ensure that the danger of fire is completely removed or substantially reduced.
  • liquid developers are generally handled by operators, it is desirable that they be non-toxic and this invention therefore seeks to provide a liquid developer for electrostatic images which is both non-inflammable and non-toxic in ordinary use.
  • Such a developer can be formed by using as the liquid carrier having the necessary high electrical resistivity, substances of the chlorofluoromethane, or ethane, group.
  • chlorinated fluorinated hydrocarbon solvents or refrigerants or propellants are the chlorinated fluorinated hydrocarbon solvents or refrigerants or propellants.
  • the substances of the invention should have a dielectric constant less than 3, preferably less than 2.5 and should be sufiiciently stable under various conditions.
  • One of the advantages of using ffuorinated hydrocarbon solvents or refrigerants or propellants is that a high degree of volatility can be attained, the effect of this being to speed up development and permitting very quick removal of the carrier medium and thereby ensuring the rapid fixing and drying of the developed image.
  • the substances are good carriers for the pigment materials, and have the necessary solvent action for the resins or other substances which may be used with liquid developers to act as control and fixing agents.
  • Example 1 15 grams of a phenol modified penta-erythritol ester of rosin such as that known under the trade name Pentarol 20 (acid value 7-15, specific gravity at 20 C. 1.09, melting range 110l20 C.) is digested'in 25 grams of Xylene (a non-polar liquid having a volume resistivity of at least 10 ohm-centimetre and a dielectric constant of less than 3), and when solution is completed, 15 grams of a linseed oil modified alkyd resin of medium oil length such as that known under the trade name Rhodene L6/ (oil length 52%, acid value 610, specific gravity at 20 C. 0955-0965) is added.
  • Xylene a non-polar liquid having a volume resistivity of at least 10 ohm-centimetre and a dielectric constant of less than 3
  • phthalocyanine blue is then added to the above coating mix and blended either in a ball mill or a triple roller mill until mixing is complete and pigment :particle size is reduced to the required fineness, such as 0.5 micron, average.
  • This coating mix will thus influence the surface charge of the coated particles and will form the bonding means after the pigment is applied in a liquid development process.
  • the paste so produced is used as the basis for a dispersion in the chlorinated fluorin-ated hydrocarbon solvent forming the developer carrier liquid, approximately 0.5 gram of the developer paste being dispersed in 100 mils of the liquid.
  • the liquid developer so formed is simply contacted with the image, and the coated pigment particles, which are free to move in the liquid, deposit on those areas of the image where a suitable potential exists, until the charge of the image has been satisfied by the particles deposited, the particles being held in position by the electrical force until the carrier liquid is evaporated, whereupon the pigment particles are held by direct adhesion of the resin on the surface of the particles.
  • the coating mix according to the above example is, as said, only partly soluble in the carrier liquid, and therefore, while the partly dissolved surface of the coating is in a condition where it will form an effective bonding medium after evaporation of the solvent, it will act as a surface charge modifier during development to control the migration of the particles in an electrical field.
  • the developer paste described is more soluble in the trichloromonofluoromethane and simple mixing, without grinding, is found suflicient.
  • a mixture of the two carriers referred to may be used, for instance 60% of Freon MP and 40% of Freon TF.
  • Freon MF or Freon TF may be combined with a less volatile, or an inflammable type of carrier provided the compounded carrier has a volume resistivity in excess of 10 ohm-centimetre and a dielectric constant of not greater than 3.
  • a suitable mixture would be Freon MF 80 parts and xylene 20 parts the resulting mixture still being non-inflammable.
  • the percent-age can, of course, be varied according to conditions.
  • Example 2 The developer of Example 1 can be modified by re- .the developer then acts as one placing the Rhodehe L6/100 with an equal percentage of Pentarol 20, whereupon it Will be found that the developer will have good fixing qualities but will not have the same degree of modification of the surface charge ofi thepigment particles as the Pentarol 20 is relatively soluble in the hydrocarbon carrier liquid and is a tacky substance, so that it tends to leave the pigment particles when in the developer and deposit :as a. fixing substance.
  • sufi'icient tacky substance is substances to cause it to remain there ment, the developer can he said to have both a charge modifying agent and a fixing agent.
  • Example 3 V The developer of example 1 has the Pentarol 20 replaced by an equal percentage of Rhodene L6/100,
  • . prising a chlorinated fluorinated hydrocarbon carrier .liquid selected from the group consisting of trichloroduring developcharge modifier for said substantial volatility to monofluoromethane and :trichlorotrifiuoroethane and mixtures thereof, pigment particles dispersed in said liquid, and resins constituting a coating on said particles, one of said resins being relatively soluble in said liquid and constituting a fixing agent for said particles whereby the particles may be fixed tola surface, another of said resins being relatively insoluble in said liquid and being of such composition as to constitute an electrostatic particles,.said liquid having a insure a rapid fixing of said particles to said surface.
  • a developer as defined in claim 1 further comprising a non-polar liquid having a volume resistivity of at least 10 ohm-centimetre and a dielectric constant of less than 3.

Description

3,058,914 Patented Oct. 16, 1962 3,058,914 NON-INFLAMll/IABLE LlQUlD DEVELOPERS FOR ELECTROSTATIC IMAGES Kenneth A. Metcalie, Graymore, South Australia, and
Robert J. Wright, Hectorville, South Australia, Australia, assiguors to The Commonwealth of Australia, Melbourne, Victoria, Australia No Drawing. Filed Sept. 24, 1958, Ser. No. 7 62,912 Claims priority, application Australia, Oct. 1, 1957 2 Claims. ((31. 252-621) This invention relates to non-inflammable liquid developers for electrostatic images.
It is already known to develop electrostatic images by applying either a dry powder to the image or by subjecting the image to liquid development in a carrier having a sufiiciently high electrical resistivity to prevent destruction of the electrostatic image during development.
Liquids having the required characteristics are generally of an inflammatory nature and while the hazard of using them is extremely small or non-existent under suitable operating conditions, an object of this invention is to provide an improvement with respect to this type of developer which will ensure that the danger of fire is completely removed or substantially reduced.
As such liquid developers are generally handled by operators, it is desirable that they be non-toxic and this invention therefore seeks to provide a liquid developer for electrostatic images which is both non-inflammable and non-toxic in ordinary use.
We have found that such a developer can be formed by using as the liquid carrier having the necessary high electrical resistivity, substances of the chlorofluoromethane, or ethane, group.
Amongst the substances which we have found of particular interest are the chlorinated fluorinated hydrocarbon solvents or refrigerants or propellants.
These substances are non-inflammable, non-explosive, are relatively non-toxic, and, provided the correct grouping is chosen, are sufficiently stable in use to permit them to be used commercially as the suspending medium for pigment or developer substance in electrostatic image development.
The substances of the invention should have a dielectric constant less than 3, preferably less than 2.5 and should be sufiiciently stable under various conditions.
One of the advantages of using ffuorinated hydrocarbon solvents or refrigerants or propellants is that a high degree of volatility can be attained, the effect of this being to speed up development and permitting very quick removal of the carrier medium and thereby ensuring the rapid fixing and drying of the developed image.
Two substances which have been found to give very favorable results are trichloromonofluoromethane (CCl F) as sold under the trademark Freon MF and trichlorotrifluoroethane (CCl -CClf sold under the trademark Freon TF. I
The substances are good carriers for the pigment materials, and have the necessary solvent action for the resins or other substances which may be used with liquid developers to act as control and fixing agents.
To enable the invention to be fully understood the following examples are given:
Example 1 15 grams of a phenol modified penta-erythritol ester of rosin such as that known under the trade name Pentarol 20 (acid value 7-15, specific gravity at 20 C. 1.09, melting range 110l20 C.) is digested'in 25 grams of Xylene (a non-polar liquid having a volume resistivity of at least 10 ohm-centimetre and a dielectric constant of less than 3), and when solution is completed, 15 grams of a linseed oil modified alkyd resin of medium oil length such as that known under the trade name Rhodene L6/ (oil length 52%, acid value 610, specific gravity at 20 C. 0955-0965) is added.
grams of phthalocyanine blue is then added to the above coating mix and blended either in a ball mill or a triple roller mill until mixing is complete and pigment :particle size is reduced to the required fineness, such as 0.5 micron, average. I
Eight hours milling in a ball mill is usually sufficient, after which it will 'be found that the pigment particles are coated with a thin film, continuous 'or discontinuous, of the coating mix one component being relatively insoluble in the carrier to act as the control agent and the other sufiifficiently soluble to act as the fixing agent when the carrier liquid is evaporated.
This coating mix will thus influence the surface charge of the coated particles and will form the bonding means after the pigment is applied in a liquid development process.
The paste so produced is used as the basis for a dispersion in the chlorinated fluorin-ated hydrocarbon solvent forming the developer carrier liquid, approximately 0.5 gram of the developer paste being dispersed in 100 mils of the liquid.
To develop an electrostatic image, the liquid developer so formed is simply contacted with the image, and the coated pigment particles, which are free to move in the liquid, deposit on those areas of the image where a suitable potential exists, until the charge of the image has been satisfied by the particles deposited, the particles being held in position by the electrical force until the carrier liquid is evaporated, whereupon the pigment particles are held by direct adhesion of the resin on the surface of the particles.
During development, the presence of the resin infiuences the particle charge, and it is found that rapid deposition is possible of the particles when they are so coated.
The coating mix according to the above example is, as said, only partly soluble in the carrier liquid, and therefore, while the partly dissolved surface of the coating is in a condition where it will form an effective bonding medium after evaporation of the solvent, it will act as a surface charge modifier during development to control the migration of the particles in an electrical field.
In the case of the trichlorotrifluoroethane it is desirable to grind the paste into the carrier liquid as otherwise solubility of the paste in the liquid will be too low and difficulty may be experienced in getting eifective adhesion of the coated pigment particles after evaporation of the carrier.
The developer paste described is more soluble in the trichloromonofluoromethane and simple mixing, without grinding, is found suflicient.
If desired, a mixture of the two carriers referred to may be used, for instance 60% of Freon MP and 40% of Freon TF. Freon MF or Freon TF may be combined with a less volatile, or an inflammable type of carrier provided the compounded carrier has a volume resistivity in excess of 10 ohm-centimetre and a dielectric constant of not greater than 3. A suitable mixture would be Freon MF 80 parts and xylene 20 parts the resulting mixture still being non-inflammable.
The percent-age can, of course, be varied according to conditions.
Example 2 The developer of Example 1 can be modified by re- .the developer then acts as one placing the Rhodehe L6/100 with an equal percentage of Pentarol 20, whereupon it Will be found that the developer will have good fixing qualities but will not have the same degree of modification of the surface charge ofi thepigment particles as the Pentarol 20 is relatively soluble in the hydrocarbon carrier liquid and is a tacky substance, so that it tends to leave the pigment particles when in the developer and deposit :as a. fixing substance.
If sufi'icient tacky substance is substances to cause it to remain there ment, the developer can he said to have both a charge modifying agent and a fixing agent.
present on the pigment r 7 Example 3 V The developer of example 1 has the Pentarol 20 replaced by an equal percentage of Rhodene L6/100,
.prising a chlorinated fluorinated hydrocarbon carrier .liquid selected from the group consisting of trichloroduring developcharge modifier for said substantial volatility to monofluoromethane and :trichlorotrifiuoroethane and mixtures thereof, pigment particles dispersed in said liquid, and resins constituting a coating on said particles, one of said resins being relatively soluble in said liquid and constituting a fixing agent for said particles whereby the particles may be fixed tola surface, another of said resins being relatively insoluble in said liquid and being of such composition as to constitute an electrostatic particles,.said liquid having a insure a rapid fixing of said particles to said surface.
2. A developer as defined in claim 1 further comprising a non-polar liquid having a volume resistivity of at least 10 ohm-centimetre and a dielectric constant of less than 3.
References Cited in the file of this patent UNITED STATES PATENTS 2,379,070 7 Evans etal June 26, 1945 2,381,753 Irion Aug. 7, 1945 2,693,391 Manseau Nov. 2, 1954 2,728,495- Eaton Dec. 27, 1955 2,731,436 Stetz et a1 Jan. 17, 1956 2,742,321 Mina et a1. Apr. 17, 1956 2,377,133 Mayer Mar. 10, 1959 3,010,842 Ricker Nov. 28, 1961 OTHER REFERENCES Metcalfe: Liquid Developers for Xerography, J. of Sci. Instruments, vol. 32, February 1955, pp. 74-75.

Claims (1)

1. A LIQUID DEVELOPER FOR ELECTROSTATIC IMAGES COMPRISING A CHLORINATED FLUORINATED HYDROCARBON CARRIER LIQUID SELECTED FROM THE GROUP CONSISTING OF TRICHLOROMONOFLUOROMETHANE AND TRICHLOROTRIFLUOROTHANE AND MIXTURES THEREOF, PIGMENT PARTICLES DISPERSED IN SAID LIQUID, AND RESINS CONSTITUTING A COATING ON SAID PARTICLES, ONE OF SAID RESINS BEING RELATIVELY SOLUBLE IN SAID LIQUID AND CONSTITUTING A FIXING AGENT FOR SAID PARTICLES WHEREBY THE PARTICLES MAY BE FIXED TO A SURFACE ANOTHER OF SAID RESINS BEING RELATIVELY INSOLUBLE IN SAID LIQUID AND BEING OF SUCH COMPOSITION AS TO CONSTITUTE AN ELECTROSTATIC CHARGE MODIFIER FOR SAID PARTICLES, SAID LIQUID HAVING A SUBSTANTIAL VOLATILITY TO INSURE A RAPID FIXING OF SAID PARTICLES TO SAID SURFACE.
US762912A 1957-10-01 1958-09-24 Non-inflammable liquid developers for electrostatic images Expired - Lifetime US3058914A (en)

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AU31770/57A AU236835B2 (en) 1958-09-17 An improved developer for electrostatic images

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Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3212916A (en) * 1957-09-25 1965-10-19 Commw Of Australia Method of developing electrostatic image with foam liquid developer
US3220830A (en) * 1961-10-02 1965-11-30 Kenffel & Esser Company Method of developing a negative electrostatic latent image
US3241998A (en) * 1960-07-12 1966-03-22 Australia Res Lab Method of fixing xerographic images
US3244633A (en) * 1961-10-24 1966-04-05 Gen Aniline & Film Corp Liquid developers for developing electrostatic images
US3296140A (en) * 1964-02-13 1967-01-03 Dick Co Ab Liquid developer for electrographic printing
US3384566A (en) * 1964-07-23 1968-05-21 Xerox Corp Method of photoelectrophoretic imaging
US3384488A (en) * 1964-07-23 1968-05-21 Xcrox Corp Polychromatic photoelectrophoretic imaging composition
US3391015A (en) * 1964-04-27 1968-07-02 Harris Intertype Corp Liquid development of electrostatic images with carbon black and a solid organic pigment
US3438904A (en) * 1966-01-10 1969-04-15 Scm Corp Liquid toner
US3507794A (en) * 1964-12-22 1970-04-21 Harris Intertype Corp Electrostatic photography systems
US3535244A (en) * 1966-04-27 1970-10-20 Dick Co Ab Liquid developer composition for electrostatic images
US3640751A (en) * 1967-11-06 1972-02-08 Ricoh Kk Method for liquid-developing an electrostatic image
US3640863A (en) * 1968-06-05 1972-02-08 Ricoh Kk A liquid electrostatic having pigment particles coated with a cyclized rubber
US3714048A (en) * 1969-10-23 1973-01-30 Iwatsu Electric Co Ltd Electrophotographic liquid developer containing asphalt and modified alkyl resin
US4285801A (en) * 1979-09-20 1981-08-25 Xerox Corporation Electrophoretic display composition
US5643707A (en) * 1995-07-31 1997-07-01 Xerox Corporation Liquid developer compositions
US5952048A (en) * 1994-06-17 1999-09-14 Ricoh Company, Ltd. Ink composition and recording method using the same
US6479205B1 (en) * 1994-10-28 2002-11-12 Indigo N.V. Imaging apparatus and toner therefor

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3150976A (en) * 1960-02-04 1964-09-29 Rca Corp Electrostatic printing
US3291738A (en) * 1960-09-02 1966-12-13 Rca Corp Materials for preparing etch resists

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US2379070A (en) * 1941-03-14 1945-06-26 Du Pont Pigment dispersions
US2381753A (en) * 1941-01-03 1945-08-07 Gen Printing Ink Corp Printing ink
US2693391A (en) * 1951-02-21 1954-11-02 David O Manseau Spray bomb
US2728495A (en) * 1951-04-19 1955-12-27 Little Inc A Liquid dispensing device and composition therefor
US2731436A (en) * 1950-02-25 1956-01-17 Engine Parts Mfg Company Metallic paint
US2742321A (en) * 1955-07-27 1956-04-17 Chemway Corp Packages of self-propelling atomizing low pressure liquid compositions
US2877133A (en) * 1956-10-22 1959-03-10 Gen Dynamics Corp Electrostatic photography
US3010842A (en) * 1955-08-29 1961-11-28 Xerox Corp Development of electrostatic images

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Publication number Priority date Publication date Assignee Title
NL95463C (en) * 1955-12-29

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2381753A (en) * 1941-01-03 1945-08-07 Gen Printing Ink Corp Printing ink
US2379070A (en) * 1941-03-14 1945-06-26 Du Pont Pigment dispersions
US2731436A (en) * 1950-02-25 1956-01-17 Engine Parts Mfg Company Metallic paint
US2693391A (en) * 1951-02-21 1954-11-02 David O Manseau Spray bomb
US2728495A (en) * 1951-04-19 1955-12-27 Little Inc A Liquid dispensing device and composition therefor
US2742321A (en) * 1955-07-27 1956-04-17 Chemway Corp Packages of self-propelling atomizing low pressure liquid compositions
US3010842A (en) * 1955-08-29 1961-11-28 Xerox Corp Development of electrostatic images
US2877133A (en) * 1956-10-22 1959-03-10 Gen Dynamics Corp Electrostatic photography

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3212916A (en) * 1957-09-25 1965-10-19 Commw Of Australia Method of developing electrostatic image with foam liquid developer
US3241998A (en) * 1960-07-12 1966-03-22 Australia Res Lab Method of fixing xerographic images
US3220830A (en) * 1961-10-02 1965-11-30 Kenffel & Esser Company Method of developing a negative electrostatic latent image
US3244633A (en) * 1961-10-24 1966-04-05 Gen Aniline & Film Corp Liquid developers for developing electrostatic images
US3296140A (en) * 1964-02-13 1967-01-03 Dick Co Ab Liquid developer for electrographic printing
US3391015A (en) * 1964-04-27 1968-07-02 Harris Intertype Corp Liquid development of electrostatic images with carbon black and a solid organic pigment
US3391014A (en) * 1964-04-27 1968-07-02 Harris Intertype Corp Liquid development of electrostatic images
US3384566A (en) * 1964-07-23 1968-05-21 Xerox Corp Method of photoelectrophoretic imaging
US3384488A (en) * 1964-07-23 1968-05-21 Xcrox Corp Polychromatic photoelectrophoretic imaging composition
US3384565A (en) * 1964-07-23 1968-05-21 Xerox Corp Process of photoelectrophoretic color imaging
US3507794A (en) * 1964-12-22 1970-04-21 Harris Intertype Corp Electrostatic photography systems
US3438904A (en) * 1966-01-10 1969-04-15 Scm Corp Liquid toner
US3535244A (en) * 1966-04-27 1970-10-20 Dick Co Ab Liquid developer composition for electrostatic images
US3640751A (en) * 1967-11-06 1972-02-08 Ricoh Kk Method for liquid-developing an electrostatic image
US3770485A (en) * 1967-11-06 1973-11-06 Ricoh Kk Method for liquid-developing an electrostatic image
US3640863A (en) * 1968-06-05 1972-02-08 Ricoh Kk A liquid electrostatic having pigment particles coated with a cyclized rubber
US3714048A (en) * 1969-10-23 1973-01-30 Iwatsu Electric Co Ltd Electrophotographic liquid developer containing asphalt and modified alkyl resin
US4285801A (en) * 1979-09-20 1981-08-25 Xerox Corporation Electrophoretic display composition
US5952048A (en) * 1994-06-17 1999-09-14 Ricoh Company, Ltd. Ink composition and recording method using the same
US6479205B1 (en) * 1994-10-28 2002-11-12 Indigo N.V. Imaging apparatus and toner therefor
US20030059701A1 (en) * 1994-10-28 2003-03-27 Benzion Landa Imaging apparatus and improved toner therefor
US20030068570A1 (en) * 1994-10-28 2003-04-10 Benzion Landa Imaging apparatus and improved toner therefor
US20080056779A1 (en) * 1994-10-28 2008-03-06 Benzion Landa Imaging Apparatus and Improved Toner Therefor
US7354691B2 (en) 1994-10-28 2008-04-08 Hewlett-Packard Development Company, L.P. Imaging apparatus and improved toner therefor
US7647008B2 (en) 1994-10-28 2010-01-12 Hewlett-Packard Indigo B.V. Imaging apparatus and improved toner therefor
US7678525B2 (en) 1994-10-28 2010-03-16 Hewlett-Packard Development Company, L.P. Imaging apparatus and improved toner therefor
US5643707A (en) * 1995-07-31 1997-07-01 Xerox Corporation Liquid developer compositions

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GB854012A (en) 1960-11-16
FR1202799A (en) 1960-01-13
CH381252A (en) 1964-08-31
DE1089631B (en) 1960-09-22

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