US3058914A - Non-inflammable liquid developers for electrostatic images - Google Patents
Non-inflammable liquid developers for electrostatic images Download PDFInfo
- 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
- Authority
- US
- United States
- Prior art keywords
- liquid
- particles
- developer
- resins
- electrostatic images
- 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
- 239000007788 liquid Substances 0.000 title claims description 33
- 239000002245 particle Substances 0.000 claims description 26
- 239000000049 pigment Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 6
- 239000003607 modifier Substances 0.000 claims description 3
- 229940029284 trichlorofluoromethane Drugs 0.000 claims description 3
- 239000000126 substance Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 5
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241000350158 Prioria balsamifera Species 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- -1 phenol modified penta-erythritol ester Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
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
- G03G9/12—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.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Liquid Developers In Electrophotography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU31770/57A AU236835B2 (en) | 1958-09-17 | An improved developer for electrostatic images |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3058914A true US3058914A (en) | 1962-10-16 |
Family
ID=3719427
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US762912A Expired - Lifetime US3058914A (en) | 1957-10-01 | 1958-09-24 | Non-inflammable liquid developers for electrostatic images |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3058914A (de) |
| CH (1) | CH381252A (de) |
| DE (1) | DE1089631B (de) |
| FR (1) | FR1202799A (de) |
| GB (1) | GB854012A (de) |
Cited By (18)
| 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 |
| US3384488A (en) * | 1964-07-23 | 1968-05-21 | Xcrox Corp | Polychromatic photoelectrophoretic imaging composition |
| US3384566A (en) * | 1964-07-23 | 1968-05-21 | Xerox Corp | Method of photoelectrophoretic imaging |
| 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 |
| US3640863A (en) * | 1968-06-05 | 1972-02-08 | Ricoh Kk | A liquid electrostatic having pigment particles coated with a cyclized rubber |
| US3640751A (en) * | 1967-11-06 | 1972-02-08 | Ricoh Kk | Method for liquid-developing an electrostatic image |
| 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)
| 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 |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE553789A (de) * | 1955-12-29 |
-
1958
- 1958-09-24 GB GB30566/58A patent/GB854012A/en not_active Expired
- 1958-09-24 US US762912A patent/US3058914A/en not_active Expired - Lifetime
- 1958-09-27 DE DEC17562A patent/DE1089631B/de active Pending
- 1958-09-29 FR FR1202799D patent/FR1202799A/fr not_active Expired
- 1958-10-01 CH CH6457058A patent/CH381252A/fr unknown
Patent Citations (8)
| 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)
| 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 |
| 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 |
| US3384566A (en) * | 1964-07-23 | 1968-05-21 | Xerox Corp | Method of photoelectrophoretic 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| GB854012A (en) | 1960-11-16 |
| DE1089631B (de) | 1960-09-22 |
| CH381252A (fr) | 1964-08-31 |
| FR1202799A (fr) | 1960-01-13 |
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