EP0160979A2 - Printing method by electrolytic colloid coagulation and colloid composition therefor - Google Patents
Printing method by electrolytic colloid coagulation and colloid composition therefor Download PDFInfo
- Publication number
- EP0160979A2 EP0160979A2 EP85105621A EP85105621A EP0160979A2 EP 0160979 A2 EP0160979 A2 EP 0160979A2 EP 85105621 A EP85105621 A EP 85105621A EP 85105621 A EP85105621 A EP 85105621A EP 0160979 A2 EP0160979 A2 EP 0160979A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- colloid
- group
- coagulated
- positive electrode
- alcohol
- 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.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/20—Duplicating or marking methods; Sheet materials for use therein using electric current
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
- B41C1/00—Forme preparation
- B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
- B41C1/105—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by electrocoagulation, by electro-adhesion or by electro-releasing of material, e.g. a liquid from a gel
Definitions
- This invention relates to printing and, more particularly, to a method of making a printing plate by electric coagulation, to an electrically-coagulable colloid composition therefor and to a method of printing ordinary paper with the printing plate.
- the patented method may suffer adverse secondary effects and speed restrictions, making it less suitable for more-demanding applications and for achieving sustained reliable performance, such as for computer printers and photocopying.
- the colloids used in the patented method make it impossible to print on ordinary paper, since it requires gelatinized paper, which is expensive.
- the albumin or gelatin used in the above-noted patent is not usually of consistent quality due to the high variance of its molecular weight and its different chemical pre-treatment, as well as its ability to be adversely affected by the bacterial decomposition in ambient air.
- the present invention includes a method of recording an image comprising the steps of interposing a thin layer in substantially--liquid state containing water, an electrolyte and an electrolytically-coagulable colloid between and in contact with a plurality of negative electrodes, and a single positive electrode, the positive electrode being electrolytically inert, successively and selectively biasing said electrodes with direct current for a short period of time and concurrently sweeping the positive electrode by the negative electrodes to thereby cause point-by-point selective coagulation and adherence of the colloid onto said positive electrode and removing the non-coagulated colloid, whereby the coagulated colloid is representative of a desired image.
- the improved method is characterized by the use of a colloid selected from the group consisting of water-dispersable synthetic linear colloid polymers, of high molecular weight, the colloid polymer being capable, when coagulated, of absorbing an agent soluble in an alcohol. More specifically, the colloid is selected from the group of water dispersable synthetic linear colloid polymers, of a molecular weight between 100,000 and 600,000 and, preferably, between 200,000 and 450,000 and including polyacrylic acid and polyacrylamide resins.
- the uniform characteristic of the synthetic colloid polymers, with a well-controlled molecular weight, has been found to provide reliably-uniform and superior results over the albumin and gelatin used in the above-noted U.S. patent.
- the electrolyte used in the composition is either an acid or a salt selected from the group consisting of lithium sodium, potassium and ammonium chloride.
- the composition also preferably includes an electrode depolarizing agent to minimize the deposition of gas against the electrodes.
- an agent is preferably selected from the group of manganese and nitrate compounds and H202, which combines with the gas produced against the electrodes upon breakdown of a water molecule into oxygen and hydrogen ions.
- Lead nitrate, manganese chloride and H 2 0 2 have been found suitable as a depolarizing agent.
- the positive electrode must be electrolytically inert. Metals suitable for making the positive electrode are selected from stainless steel, aluminum and tin, with stainless steel 316 being preferred as giving the best results.
- the non-coagulated colloid composition is removed by washing or scraping the positive electrode with a soft rubber squeegee, and this is followed by the step of coloring the coagulated synthetic dots with a water-soluble dye to form the printing plate.
- the coloring step includes preparing a water solution of the dye with a solvent for the synthetic linear colloid polymer, thus constituting a swelling agent for the coagulated dots of the printing plate. This swelling agent is applied to the printing plate and the coagulated dots become swollen as they absorb the solvent and absorb the dye. After removing the surplus of the dyed solution, the swelled dyed, coagulated image is pressed in close contact with ordinary paper previously slightly wetted with an alcohol.
- the swelling agent is soluble in the alcohol, the dye of the dots is transferred onto the paper surface.
- Any ordinary paper can thus be printed, including uncoated paper, such as bond paper and coated paper, more specifically kaolin-coated and synthetic resin-coated paper.
- the preferred swelling agent is a water solution of a compound selected from the group consisting of one or more of glycerol, ethylene glycol and sorbitol. These compounds act as a solvent for polyacrylic acid and polyacrylamide resin, and they are also soluble in the alcohol used for wetting the paper to be printed.
- Preferred alcohols for such paper wetting are selected from the group consisting of methanol, ethanol and isopropylic alcohol. These alcohols possess high paper wetting property and, therefore, the colored glycerol or ethylene glycol or sorbitol, or mixtures thereof, are absorbed by the paper fibers where they remain.
- the dye transfer processing on paper just described cannot work with the gelatin and albumin colloids mentioned in the above-noted U.S. patent. Sorbitol and ethylene glycol have only a very slight swelling effect on gelatin or albumin and are totally unsatisfactory for the above-described printing step. Gelatinized paper must be used to effect printing from the printing plate where the coagulated dots are gelatin or albumin.
- This water solution has a pH of 2.25.
- This solution was used as a layer between the negative and positive electrodes in the above-described method for recording an image.
- the positive electrode was stainless steel 316.
- the gap between the negative and positive electrodes was 50 microns.
- the negative electrodes were copper-insulated wires of 250 microns in diameter arranged in a linear array.
- the electrodes were successively biased by successively and selectively applying to the negative electrodes a power supply of 25 watts (50 volts and 500 milliamperes).
- the operating temperature was 30°C.
- a speed of coagulation of 300,000 dots per second was achieved, with the size of the dots being 250 microns in diameter. This means that an electric p . ⁇ se at each electrode of one-three hundred thousandths of a second was necessary to effect coagulation.
- the experiment was repeated several times and the coagulation results were very constant from one experiment to the other. Additional experiments were repeated using the same liquid composition but using negative electrodes having a diameter of 125 microns instead of 250 microns. The resulting speed of coagulation was found to be 1,000,000 dots per second, that is requiring an electrical pulse for each negative electrode of one millionth of a second.
- liquid electrolytically-coagulable colloid composition of any of the above noted examples, was added a depolarizing agent consisting of two percent by weight of a compound selected from lead nitrate, manganese chloride and H202, with ever better results.
- the coagulated synthetic resin dots of the printing plate obtained from any of the foregoing examples were swollen and colored by applying thereto the following solution: water soluble dye selected from Pina dyes and obtained
- the glycerol acts as a solvent of the polyacrylic acid, or polyacrylamide resin, the coagulated dots became swollen and absorbed the dye. The surplus dye solution was then removed and the swelled, dyed coagulated image was pressed in close contact with a kaolin-coated paper previously wetted with methanol.
- the methanol which is a solvent for glycerol, caused the transfer of the dye to the paper surface, resulting in the image transfer to the paper.
- About seven paper sheets were thus printed with the same printing plate, while recharging the synthetic dots with the dye and swelling agent each time; it was found that up to about seven sheets could be printed. To print additional sheets, it was necessary to remake the printing plate.
- the paper wetting agent was ethanol and similar results as in Example V were obtained.
- Example VI The same experiments as Example VI were carried out but using the following coloring and swelling agent composition for treating the coagulated dots of the printing plate image:
- Isopropylic alcohol was used as the paper wetting agent.
- the dye transfer to the paper was less than in Examples V and VI, since sorbitol is a poorer solvent and, therefore, a poorer swelling agent than glycerol or ethylene glycol for the coagulated dots of the colloids named in Examples I to IV.
- sorbitol when admixed with either or both glycerol and ethylene glycol, the coagulated colloid swelling efficiency can be adjusted for maximum dye transfer to the paper.
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Colloid Chemistry (AREA)
- Cosmetics (AREA)
- Manufacture Or Reproduction Of Printing Formes (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Printing Methods (AREA)
- Printing Plates And Materials Therefor (AREA)
Abstract
Description
- This invention relates to printing and, more particularly, to a method of making a printing plate by electric coagulation, to an electrically-coagulable colloid composition therefor and to a method of printing ordinary paper with the printing plate.
- In applicant's United States patent number 3,892,645 dated July 1, 1975 and entitled: "PRINTING METHOD AND SYSTEM BY GELATIN COAGULATION", there is defined a method for recording an image including coagulation of a colloid composition. Electric direct current is passed at desired places through a thin layer of a liquid-state colloid composition containing an electrolyte, by means of several negative electrodes and a single positive electrolytically--inert electrode in contact with the layer, thus achieving coagulation and adherence of part of the colloid to the positive electrode and removing the non-coagulated colloid composition to leave only the coagulated image.
- It has been found that the patented method may suffer adverse secondary effects and speed restrictions, making it less suitable for more-demanding applications and for achieving sustained reliable performance, such as for computer printers and photocopying. Also, the colloids used in the patented method make it impossible to print on ordinary paper, since it requires gelatinized paper, which is expensive. More specifically, it has been found that the albumin or gelatin used in the above-noted patent is not usually of consistent quality due to the high variance of its molecular weight and its different chemical pre-treatment, as well as its ability to be adversely affected by the bacterial decomposition in ambient air.
- It is the general object of the invention to obviate the above-noted disadvantages.
- It is another object of the invention to use in the above-noted method an improved electrically-coagulable colloid composition.
- It is another object of the present invention to provide a method of recording an image by electric coagulation, thus forming a printing plate, and printing ordinary paper therewith, the method achieving an increased printing speed and increased reliability suitable for computer printing and photocopying.
- As in the above-noted U.S. patent, the present invention includes a method of recording an image comprising the steps of interposing a thin layer in substantially--liquid state containing water, an electrolyte and an electrolytically-coagulable colloid between and in contact with a plurality of negative electrodes, and a single positive electrode, the positive electrode being electrolytically inert, successively and selectively biasing said electrodes with direct current for a short period of time and concurrently sweeping the positive electrode by the negative electrodes to thereby cause point-by-point selective coagulation and adherence of the colloid onto said positive electrode and removing the non-coagulated colloid, whereby the coagulated colloid is representative of a desired image. The improved method is characterized by the use of a colloid selected from the group consisting of water-dispersable synthetic linear colloid polymers, of high molecular weight, the colloid polymer being capable, when coagulated, of absorbing an agent soluble in an alcohol. More specifically, the colloid is selected from the group of water dispersable synthetic linear colloid polymers, of a molecular weight between 100,000 and 600,000 and, preferably, between 200,000 and 450,000 and including polyacrylic acid and polyacrylamide resins. The uniform characteristic of the synthetic colloid polymers, with a well-controlled molecular weight, has been found to provide reliably-uniform and superior results over the albumin and gelatin used in the above-noted U.S. patent. The electrolyte used in the composition is either an acid or a salt selected from the group consisting of lithium sodium, potassium and ammonium chloride. The composition also preferably includes an electrode depolarizing agent to minimize the deposition of gas against the electrodes. Such an agent is preferably selected from the group of manganese and nitrate compounds and H202, which combines with the gas produced against the electrodes upon breakdown of a water molecule into oxygen and hydrogen ions. Lead nitrate, manganese chloride and H202 have been found suitable as a depolarizing agent. The positive electrode must be electrolytically inert. Metals suitable for making the positive electrode are selected from stainless steel, aluminum and tin, with stainless steel 316 being preferred as giving the best results. The non-coagulated colloid composition is removed by washing or scraping the positive electrode with a soft rubber squeegee, and this is followed by the step of coloring the coagulated synthetic dots with a water-soluble dye to form the printing plate. The coloring step includes preparing a water solution of the dye with a solvent for the synthetic linear colloid polymer, thus constituting a swelling agent for the coagulated dots of the printing plate. This swelling agent is applied to the printing plate and the coagulated dots become swollen as they absorb the solvent and absorb the dye. After removing the surplus of the dyed solution, the swelled dyed, coagulated image is pressed in close contact with ordinary paper previously slightly wetted with an alcohol. Since the swelling agent is soluble in the alcohol, the dye of the dots is transferred onto the paper surface. Any ordinary paper can thus be printed, including uncoated paper, such as bond paper and coated paper, more specifically kaolin-coated and synthetic resin-coated paper. The preferred swelling agent is a water solution of a compound selected from the group consisting of one or more of glycerol, ethylene glycol and sorbitol. These compounds act as a solvent for polyacrylic acid and polyacrylamide resin, and they are also soluble in the alcohol used for wetting the paper to be printed.
- Preferred alcohols for such paper wetting are selected from the group consisting of methanol, ethanol and isopropylic alcohol. These alcohols possess high paper wetting property and, therefore, the colored glycerol or ethylene glycol or sorbitol, or mixtures thereof, are absorbed by the paper fibers where they remain. The dye transfer processing on paper just described cannot work with the gelatin and albumin colloids mentioned in the above-noted U.S. patent. Sorbitol and ethylene glycol have only a very slight swelling effect on gelatin or albumin and are totally unsatisfactory for the above-described printing step. Gelatinized paper must be used to effect printing from the printing plate where the coagulated dots are gelatin or albumin.
- The following electrolytically-coagulable colloid composition was prepared:
- Polyacrylic acid (Carbopol 907 of B.F. Goodrich) molecular weight 450,000
- This water solution has a pH of 2.25. This solution was used as a layer between the negative and positive electrodes in the above-described method for recording an image. The positive electrode was stainless steel 316. The gap between the negative and positive electrodes was 50 microns. The negative electrodes were copper-insulated wires of 250 microns in diameter arranged in a linear array. The electrodes were successively biased by successively and selectively applying to the negative electrodes a power supply of 25 watts (50 volts and 500 milliamperes). The operating temperature was 30°C. A speed of coagulation of 300,000 dots per second was achieved, with the size of the dots being 250 microns in diameter. This means that an electric p .Ùse at each electrode of one-three hundred thousandths of a second was necessary to effect coagulation.
- The experiment was repeated several times and the coagulation results were very constant from one experiment to the other. Additional experiments were repeated using the same liquid composition but using negative electrodes having a diameter of 125 microns instead of 250 microns. The resulting speed of coagulation was found to be 1,000,000 dots per second, that is requiring an electrical pulse for each negative electrode of one millionth of a second.
- Comparative experiments were made using the same set-up but with gelatin and albumin as the colloid. The coagulation was very inconsistent from one experiment to the other, and the speed of coagulation using 250 microns negative electrodes was only 100,000 dots per second.
- A series of experiments were conducted for recording an image using the same electrolytically-coagulable colloid composition, but with the polyacrylic acid mentioned in Example I replaced by a polyacrylic acid of molecular weight of 250,000 as supplied by Aldrich under code number 18128-5, with the resulting solution having a pH adjusted to 2,30. Very similar results were obtained: other experiments were carried out and with similar results using the following colloid polymer: Polyacrylamide of molecular weight 200.000, supplied by
- Aldrich under code number 19-092-6, with the solution adjusted to a pH of 4,46.
- Additional experiments were carried out with the same results, using a polyacrylamide of molecular weight 250,000, as supplied by Cyanamid under code name ACCOSTRENGTH 86, with the solution adjusted to pH 4,63.
- Experiments similar to those of the prior-mentioned examples were carried out, but while varying the voltage applied to the electrodes; it was found that the size or thickness of the coagulated dots varied in proportion to the applied voltage, thus permitting the reproduction of half-tones.
- To the liquid electrolytically-coagulable colloid composition of any of the above noted examples, was added a depolarizing agent consisting of two percent by weight of a compound selected from lead nitrate, manganese chloride and H202, with ever better results.
-
- Since the glycerol acts as a solvent of the polyacrylic acid, or polyacrylamide resin, the coagulated dots became swollen and absorbed the dye. The surplus dye solution was then removed and the swelled, dyed coagulated image was pressed in close contact with a kaolin-coated paper previously wetted with methanol. The methanol, which is a solvent for glycerol, caused the transfer of the dye to the paper surface, resulting in the image transfer to the paper. About seven paper sheets were thus printed with the same printing plate, while recharging the synthetic dots with the dye and swelling agent each time; it was found that up to about seven sheets could be printed. To print additional sheets, it was necessary to remake the printing plate.
- Each time a paper sheet was printed, there was not only a dye transfer but also a transfer of a portion of the coagulated dots. Very precise and clear images were obtained on the paper sheets.
-
- The paper wetting agent was ethanol and similar results as in Example V were obtained.
-
- Isopropylic alcohol was used as the paper wetting agent. The dye transfer to the paper was less than in Examples V and VI, since sorbitol is a poorer solvent and, therefore, a poorer swelling agent than glycerol or ethylene glycol for the coagulated dots of the colloids named in Examples I to IV. However, it was found that sorbitol, when admixed with either or both glycerol and ethylene glycol, the coagulated colloid swelling efficiency can be adjusted for maximum dye transfer to the paper.
- The same experiments as in Examples V, VI, and VITI: were carried out, but the printing step was carried out on bond paper. This necessitated heating the printed sheet by hot-blown air to accelerate its drying, in order to prevent spreading of the dye through the paper fibers.
- Experiments were carried out in accordance with using the voltage variation of Example III in Example I or II or IV, followed by paper printing in accordance with anyone of Examples V, VI, VII, and VIII, and the printed image exhibited the 64 grades of half-tones as required for image printing in photographic work.
Claims (18)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT85105621T ATE61764T1 (en) | 1984-05-11 | 1985-05-08 | PRINTING METHOD BY ELECTROCOAGULATION OF COLLOIDS AND COLLOID COMPOSITION THEREOF. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60955584A | 1984-05-11 | 1984-05-11 | |
US609555 | 1984-05-11 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0160979A2 true EP0160979A2 (en) | 1985-11-13 |
EP0160979A3 EP0160979A3 (en) | 1987-08-12 |
EP0160979B1 EP0160979B1 (en) | 1991-03-20 |
Family
ID=24441277
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP85105621A Expired - Lifetime EP0160979B1 (en) | 1984-05-11 | 1985-05-08 | Printing method by electrolytic colloid coagulation and colloid composition therefor |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0160979B1 (en) |
JP (1) | JPS60245592A (en) |
KR (1) | KR850008299A (en) |
AT (1) | ATE61764T1 (en) |
AU (1) | AU578092B2 (en) |
BR (1) | BR8502230A (en) |
CA (1) | CA1250249A (en) |
DE (1) | DE3582188D1 (en) |
ES (1) | ES8605417A1 (en) |
ZA (1) | ZA853270B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0161633A2 (en) * | 1984-05-16 | 1985-11-21 | ELCORSY, Inc. | Image reproduction by in plane electro-coagulation of a colloid |
EP0235700A1 (en) * | 1986-02-20 | 1987-09-09 | ELCORSY, Inc. | Monochromic and polychromic printing of an image reproduced by electro-coagulation of a colloid |
EP0253358A2 (en) * | 1986-07-18 | 1988-01-20 | ELCORSY, Inc. | Method of preventing undesirable gas generation between electrodes of an electroco-agulation printing system |
EP0326115A2 (en) * | 1988-01-25 | 1989-08-02 | Canon Kabushiki Kaisha | Image forming method, recording material and image forming apparatus |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5055380A (en) * | 1989-12-18 | 1991-10-08 | Eastman Kodak Company | Method of forming a color-differentiated image utilizing a metastable aggregated group ib metal colloid material |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3752746A (en) * | 1972-02-25 | 1973-08-14 | A Castegnier | Electrolytic printing method and system |
US4165741A (en) * | 1975-12-29 | 1979-08-28 | Process Shizai Co., Ltd. | Heat-sensitive recording materials and recording process of using the same |
EP0160920A2 (en) * | 1984-05-08 | 1985-11-13 | Hoechst Aktiengesellschaft | One-step electrochemical image-forming process for reproduction sheets |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3892645A (en) * | 1973-06-06 | 1975-07-01 | Adrien Castegnier | Printing method and system by gelatin coagulation |
-
1985
- 1985-04-25 CA CA000480015A patent/CA1250249A/en not_active Expired
- 1985-05-01 ZA ZA853270A patent/ZA853270B/en unknown
- 1985-05-06 KR KR1019850003073A patent/KR850008299A/en not_active Application Discontinuation
- 1985-05-07 AU AU42059/85A patent/AU578092B2/en not_active Ceased
- 1985-05-08 AT AT85105621T patent/ATE61764T1/en not_active IP Right Cessation
- 1985-05-08 DE DE8585105621T patent/DE3582188D1/en not_active Expired - Lifetime
- 1985-05-08 EP EP85105621A patent/EP0160979B1/en not_active Expired - Lifetime
- 1985-05-10 JP JP60098140A patent/JPS60245592A/en active Granted
- 1985-05-10 BR BR8502230A patent/BR8502230A/en unknown
- 1985-05-11 ES ES543069A patent/ES8605417A1/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3752746A (en) * | 1972-02-25 | 1973-08-14 | A Castegnier | Electrolytic printing method and system |
US4165741A (en) * | 1975-12-29 | 1979-08-28 | Process Shizai Co., Ltd. | Heat-sensitive recording materials and recording process of using the same |
EP0160920A2 (en) * | 1984-05-08 | 1985-11-13 | Hoechst Aktiengesellschaft | One-step electrochemical image-forming process for reproduction sheets |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0161633A2 (en) * | 1984-05-16 | 1985-11-21 | ELCORSY, Inc. | Image reproduction by in plane electro-coagulation of a colloid |
EP0161633A3 (en) * | 1984-05-16 | 1987-08-05 | Elcorsy, Inc. | Image reproduction by in plane electro-coagulation of a colloid |
EP0235700A1 (en) * | 1986-02-20 | 1987-09-09 | ELCORSY, Inc. | Monochromic and polychromic printing of an image reproduced by electro-coagulation of a colloid |
EP0253358A2 (en) * | 1986-07-18 | 1988-01-20 | ELCORSY, Inc. | Method of preventing undesirable gas generation between electrodes of an electroco-agulation printing system |
EP0253358A3 (en) * | 1986-07-18 | 1988-12-14 | Elcorsy, Inc. | Method of preventing undesirable gas generation between electrodes of an electroco-agulation printing system |
EP0326115A2 (en) * | 1988-01-25 | 1989-08-02 | Canon Kabushiki Kaisha | Image forming method, recording material and image forming apparatus |
EP0326115A3 (en) * | 1988-01-25 | 1991-01-02 | Canon Kabushiki Kaisha | Image forming method, recording material and image forming apparatus |
US5142306A (en) * | 1988-01-25 | 1992-08-25 | Canon Kabushiki Kaisha | Image forming apparatus and method for applying an adhesive recording material to an electrode |
Also Published As
Publication number | Publication date |
---|---|
EP0160979B1 (en) | 1991-03-20 |
CA1250249A (en) | 1989-02-21 |
AU4205985A (en) | 1985-11-14 |
KR850008299A (en) | 1985-12-16 |
ES543069A0 (en) | 1986-03-16 |
BR8502230A (en) | 1986-01-14 |
JPS60245592A (en) | 1985-12-05 |
ATE61764T1 (en) | 1991-04-15 |
ES8605417A1 (en) | 1986-03-16 |
EP0160979A3 (en) | 1987-08-12 |
AU578092B2 (en) | 1988-10-13 |
DE3582188D1 (en) | 1991-04-25 |
JPH0548750B2 (en) | 1993-07-22 |
ZA853270B (en) | 1985-12-24 |
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