US3875023A - Electrorecording paper - Google Patents

Electrorecording paper Download PDF

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Publication number
US3875023A
US3875023A US320820A US32082073A US3875023A US 3875023 A US3875023 A US 3875023A US 320820 A US320820 A US 320820A US 32082073 A US32082073 A US 32082073A US 3875023 A US3875023 A US 3875023A
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Prior art keywords
recording paper
layer
electroconductive
color
paper according
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Yoichi Sekine
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Panasonic Holdings Corp
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Matsushita Electric Industrial Co Ltd
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Priority claimed from JP47034762A external-priority patent/JPS5133743B2/ja
Priority claimed from JP47054666A external-priority patent/JPS5133744B2/ja
Priority claimed from JP47092644A external-priority patent/JPS5116154B2/ja
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Priority to US05/718,989 priority Critical patent/USRE29427E/en
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    • 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
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00—Stock material or miscellaneous articles
    • Y10S428/913—Material designed to be responsive to temperature, light, moisture
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
    • Y10T428/24835—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including developable image or soluble portion in coating or impregnation [e.g., safety paper, etc.]

Definitions

  • Processes for converting electric signals directly to visible images have quickly been diversified in recent years, and processes which are practiced at present are ink recording, photochemical recording, electrolytic recording, thermal recording and dry discharge recording processes. These processes, however, individually have their merits and demerits. Recording papers for use in the said processes are desirably such that they are usable in the light, can give records high in gradation at a high speed, are stably storable without discoloration or fading, are inexpensive, and require no such operation as exchange of heads or injection of inks.
  • an electrorecording paper As a recording paper which can substantially satisfy the above-mentioned conditions, there has been proposed an electrorecording paper.
  • This recording paper has a color-developing layer containing a component capable of being colored or discolored by application of heat.
  • the said coloring component When an electric current is applied to the color-developing layer, the said coloring component is colored due to the heat energy emitted at the time of application of electric current to give a visible record at a selective portion of the color-developing layer to which the electric current has been applied.
  • the above-mentioned recording paper is prepared by providing an electroconductive layer on a support, and then forming a color-developing layer on the surface of the electroconductive layer.
  • the electrorecording paper has such characteristics as mentioned below over a spark destructive recording paper, which is similar in structure thereto and which can be subjected to high speed recording.
  • the spark destruction recording paper is prepared by forming a colored layer, an electroconductive layer composed of carbonor metal-deposited film, and a shielding layer in this order on a support.
  • This recording paper is of such a type that the shielding layer and the electroconductive layer are removed by discharge to make the lower colored layer visible. Accordingly, a large amount of pigment is required in order to shield the electroconductive layer and the colored layer, with the result that the generation of offensive odor and the formation of recording dregs are necessarily brought about due to discharge at the time of recording.
  • the aforesaid electrorecording paper is of such a type that when an electric current is applied, a colored or discolored record is formed in the color-developed layer itself, and hence has such characteristics that no colored layer or shielding layer is required, and the generation of offensive odor or fume or the formation of recording dregs is scarcely brought about at the time of recording so that there is no such fear that the equipments used are stained.
  • this recording paper is a dry recording paper, and hence has such characteristics that it does not require any such preservation vessel as required in the case of wet recording paper and is scarcely affected by temperature and humidity, and that it can always be subjected to recording under definite conditions.
  • the electrorecording paper has such drawback that when an electric current is applied from a recording needle electrode to the color-developing layer, a partial discharge takes place between the recording needle electrode and the electroconductive layer, with the result that there is obtained in the color-developing layer only a recorded mark having an area smaller than the contact area of said layer with the recording needle electrode, and thus the recorded mark is lowered in visible density.
  • the present invention aims to improve the said electrorecording paper so as to dismiss such drawbacks as mentioned above.
  • the present invention provides such electrorecording paper that the color-developing layer of the recording paper has been rendered electroconductive to avoid the occurrence of discharge at the time of application of electric current, thereby giving a record faithful to the trace of recording needle electrode.
  • the recording paper of the present invention is characterized in that an electroconductive substance has been dispersed in the color-developing layer thereof formed by dispersing in a binder a component capable of being colored by application of heat.
  • the recording paper of the present invention in the case of the recording paper of the present invention, an electric current flows through the electroconductive substance in the color-developing layer, so that the electroconductive substance generates heat and the coloring component around the electroconductive substance is colored due to the generated heat energy to give a visible record. Accordingly, the addition of the electroconductive substance results in such advantages that the recording voltage can be made lower and, since the electric current flows through the electroconductive substance without occurrence of discharge, a record having an area substantially identical with the contact area of the recording needle with the recording paper can be obtained, and thus the recorded image is increased in visible density.
  • FIG. 1 is a drawing showing the fundamental structure of the recording paper according to the present invention.
  • FlG. 2 is a drawing showing the manner of recording an image on the recording paper.
  • FIGS. 3 to 5 are drawings showing other structures of the recording paper.
  • l is a support which is a paper, cloth, glass or plastic film
  • 2 is color-developing layer which develops a color to give a visible image due to the heat energy generated in response to an electric signal, and has been formed by dispersing in a binder fine particles of a component capable of being colored by application of heat and an electroconductive substance
  • 3 is a recording needle electrode
  • 4 is another electrode faced to the electrode 3.
  • FIG. 3 shows another structure of the recording paper of the present invention in which an electroconductive layer 8 has been disposed between the support 1 and the color-developing layer 2.
  • the electroconductive layer 8 is composed of a metal-deposited film, cuprous iodide layer or carbon-coated layer, and is made higher in electric conductivity than the colordeveloping layer 2.
  • Preferable surface resistivity of this layer is Q or less at a temperature of 20C. and a relative humidity of 65%.
  • H0. 4 shows a structure of the present recording paper in which the color-developing layer 2 has been formed on an electroconductive support I such as a carbon fiberor carbon powder-incorporated paper. Preferable surface resistivity of the support 1' in 10 Q or less.
  • FIG. 5 shows a structure which is fundamentally identical with that shown in FIG. 3 but is different therefrom in that a second color-developing layer 2' has been formed between the color-developing layer 2 and the electroconductive layer 8.
  • the colordeveloping layer 2' contains no electroconductive substance, and is composed of fine particles dispersed in a binder of a component capable of being colored by application of heat.
  • the recording paper of the structure shown in FIG. 5 has, below the colordeveloping layer 2, the second color-developing layer 2 containing no electroconductive substance, and hence has such effect that the color-developing layer 2 develops a color due to the electric current flowed from the color-developing layer 2 to the electroconductive layer 8 through the color-developing layer 2', whereby the density of recorded image is increased.
  • thermorecording material capable of forming a color by application of heat, the electroconductive substance, and the binder, are explained below.
  • TH ERMORECORDlNG MATERIAL This material develops a color by utilization of the heat energy generated at the time of application of electric current.
  • a reaction compound of an electron donor with an electron acceptor For example, ferric stearate as the electron donor and pyrogallol as the electron acceptor are independently dispersed in a binder, and the binder is softened by application of heat to melt the ferric stearate, whereby a record can be obtained.
  • the record obtained in this case is a dark brown record.
  • thermorecording material there is used the combination of a leuco body of such a triphenylmethane type dye as Crystal Violet Lactone or a leuco body of a fluoran type dye with an organic acid or a phenolic acidic substance, or the combination of an organic compound having metal ions with an organic spot reagent. There is adopted the procedure that the said dye and organic acid, or said organometallic compound and organic spot reagent, are independently dispersed in a binder.
  • the color-forming dye used is a leuco body of triphenylmethane type dye represented by the below-mentioned general formula (I) or a leuco body of fluoran type dye represented by the below-mentioned general formula (ll).
  • R,, R, and R are individually a hydrogen or halogen atom, or a hydroxyl, alkyl, nitro, amino, dialkylamino, monoalkylamino or aryl group; and Z is an atom necessary to form a heterocyclic ring, and is O or Concrete examples of the above-mentioned compounds are as shown below.
  • Coupler Preferable as the coupler capable of forming a dye by chemical reaction with the color-forming dye mentioned in the preceding item (a) is a phenolic compound or an organic acid. It is desirable that the said compound or acid is solid at room temperature and can liquefy or vaporize at above C.
  • phenolic compound examples include as follows: 3,5-Xylenol, thymol, 4-tert-butylphenol, 4-
  • hydroxyacetophenone a-naphthol, B-naphthol, catechol, hydroquinone, resorcinol, 4-tert-octylcatechol, 4,4-sec-butylidenediphenol, 2,2'-dihydroxydiphenyl,
  • Organic spot reagent and organic metal salt The organic spot reagent referred to herein is a compound capable of being colored or discolored by reaction with metal ions. At present, a large number of such compounds are known. ln the present invention, however, there is utilized the phenomenon that at least one of the organic spot reagent and the metal used in combination therewith is melted due to the heat energy generated at the time of application of electric current and the two react with each other to form a color. lt is therefore desirable that one of the two which is lower in melting point is solid at below 70C. and has a melting point of 150C. or less. ln this respect, metallic soap is most preferable as the organic metal salt. Combinations of the organic spot reagent and the metal are as follows:
  • Diphenylthiocarbazide Cu, Fe, Mg or l-lg Dimethylglyoxime: Cu, Fe or Ni Benzoinoxime: Cu 8-l-lydroxyquinoline: Cd, Cu, Fe, Pb, Mn, Ni or Zn Dinitrophenylcarbazide: Cd Rhodanine: Cu or Hg Diphenylthiocarbazone: Cu, Ba, Co, Fe, Pb, Hg or Zn Diphenylcarbazone: Co, Cu, Pb, Mg, Mn, Hg, Ni or Dithiooxamide: Co, Cu, Pb or Ni 2-Mercapto-4-phenylthiazole: Co or Pb 3,5-Dimethylpyrazole: Co wNaphthylamine-dithiocarbamic acid: Co or Fe Benzoinoxime: Cu
  • Benzidine Cu.
  • Pb or Mn p-Dimethylaminobenzylidene rhodanine Cu, Fe, Mg
  • organic metal salt a metallic soap having the aforesaid metal ions is effective.
  • Typical examples of the combinations of organic spot reagents with organic metal salts, and color tones of colors developed by use of said combinations, are shown below.
  • Organic spot reagent Organic metal salt (Color tone of developed color) Dimethylglyoxime: Nickel stearate (Pink) Benzoinoxime: Copper myristate (Yellowish green) Dithiooxamide: Nickel stearate (Purple) 8-l-lydroxyquinoline: Iron oleate (Black) Gallic acid: Ferric stearate (Black) Alizarin: Copper oleate (Purplish red) Quinalizarin: Copper oleate (Purplish red) Diphenylcarbazone: Copper stearate (Red) Diphenylcarbazone: Cadmium stearate (Red) Diphenylcarbazone: Copper myristate (Purple) Diphenylcarbazone: Zinc palmitate (Deep red) Diphenylthiocarbazide: Mercuric stearate (Purple) Diphenylthiocarbazide: Lead myristate (Deep red) d
  • redox indicator s substance which has heretofore been known as redox indicator, forms a color in the vicinity of recording needle at the time of application of electric current, and it has been confirmed that said substance is effective as a color-forming material for use in electrorecording paper.
  • the redox indicator referred to herein is a substance which is colored or discolored due to oxidation with the heat generated at the time of application of electric current, and is a leuco body is preferable in view of the whiteness of the background. Examples of the redox indicators used in the present invention, and color tones of colors developed by said indicators, are shown below.
  • Leucoethyl Nile Blue (Blue) Leucomethyl Capryl Blue (Blue) Leucotoluidine Blue (Purple) Leucodiphenylamine (Purple) Leuco-N-methyldiphenylamine-p-sulfonic (Reddish purple) Leucophenylanthranilic acid (Redish purple) Triphenyltetrazolium chloride (Red) Methylviologen (Purple) Leucosafranine T (Red) Leucoindigosulfonic acid (Blue) Leucophenosafranine (Red) Leucomethylene Blue (Blue) Leucodiphenylbenzidine (Purple) Leucoerioglucine A (Yellowish green to Red) beuco-p-nitrodiphenylamine (Purple) Leucodiphenylamine-o,o'-diphenylcarboxylic (Bluish purple) 2.
  • the electroconductive substance used in the present invention is a material which is incorporated into the color-developing layer of recording paper to impart electroconductivity to said layer.
  • the surface resistivity of the colordeveloping layer is required to be 10 n or less at a temperature of 20C. and a relative humidity of It is desirable that the electroconductive substance, which is to be incorporated into the color-developing layer, is scarely affected in electric conductivity by temperature and humidity, and is transparent and white or palecolored so that the resulting recorded image can be enhanced in contrast.
  • the resistivity of the electroconductive substance is desirably 10 0 cm. or less.
  • electroconductive substance there is used a known semiconductor which is white or pale-colored, or a material prepared by coating an electroconductive film on the surface of a powder comprising a white or pale-colored substrate.
  • Electroconductive substances preferable for use in the recording papers of the present invention are shown below.
  • Cuprous iodide Cuprous iodide is obtained as a transparent or pale yellow compound, and hence is most preferable as the electroncudctive substance used in the present inven tion. It is desirable that a recording paper satisfies such demand that it does not give an impression of specific paper but is undistinguishable in appearance from ordinary paper.
  • cuprous iodide is used as the electroconductive substance to be incorporated into the colordeveloping layer, it is possible to obtain a recording paper which can satisfy the above-mentioned demand. Even when an image recorded on the present recording acid acid acid
  • cuprous iodide As the electroconductive substance is subjected to copying by use of a transmitted light, the cuprous iodide does not bring about any injury at all. in case the cuprous iodide is used to form the electroconductive layer 8 in the case where the recording paper has such a structure as shown in FIG. 3 or 5, an image recorded on the recording paper can be reproduced by utilization of a transmitted light.
  • Cuprous iodide is prepared, for example, in the following manner:
  • Tin dioxide is a white powder insoluble in water and organic solvents. [n the examples shown later was used tin dioxide having a resistivity of 2.3 X 10 (I cm.
  • This tin dioxide can be lowered in resistivity when antimony is diffused therein.
  • 50 g. of the above-mentioned tin dioxide is mixed with cc. of a 10% methanol solution of antimony trichloride, and the resulting mixture is dried at 60C. and then calcined for about 30 minutes in an electric furnace at 300 to 400C. to obtain tin dioxide.
  • the thus obtained tin dioxide having antimony diffused therein is a pale blue powder and has a resistivity of 20 to 40 0 cm.
  • Silver iodide An aqueous potassium iodide solution is mixed with an aqueous silver nitrate solution, and the resulting mixed solution is stirred to deposit a pale yellow precipitate. This precipitate is recovered by filtration, washed 2 to 3 times with water, and then dried to obtain silver iodide having a resistivity of 7.8 X 10 .0 cm.
  • a transparent and white or pale-colored substance which itself has no electric conductivity but is pulverizable into fine particles of less than about 20 microns,
  • Nesa (SnO Sb) film may also be used by coating on the surface thereof a Nesa (SnO Sb) film or a zincor aluminumdeposited film.
  • a mixed solution comprising 150 cc. of water, cc. of methanol and 20 cc. of 35% hydrochloric acid are added 100 g. of tin tetrachloride, 3 g. of antimony trichloride and 500g. of silica gel, and the resulting mixture is pulverized in a ball mill for 24 hours to form a dispersion. This dispersion is dried at 100C. and then calcined for 10 minutes in an electric furnace at 600C.
  • the calcination product is washed with a 3:] mixture of water and methanol to remove excess tin tetrachloride and antimony trichloride, and then dried to obtain a white fine powder of silica gel coated with Nesa film.
  • the thus obtained powder has a resistivity of 3.5 X I0 I! cm.
  • a white substance such as zinc oxide, titanium dioxide, magnesium carbonate, calcium oxide or lead carbonate is pulverized into particles of 5 to 10 microns, and a vapor of zinc or aluminum is deposited on the particles with stirring, whereby a gray or white fine powder having a resistivity of 2 X l0 (1 cm. to 10 fl cm. is obtained.
  • the thus obtained powder may also be used as the electroconductive substance.
  • BINDER In order to disperse in the state of fine particles the color-forming dye, coupler, organic spot reagent and organic metal salt used in the color-developing layer, and/or the electroconductive substance, and to impart bonding ability thereto, there is used a binder. Since most of the above-mentioned color-forming dye, coupler, organic spot reagent and electroconductive substance are water-insoluble, the use of a water-soluble binder is effective. Further, the water-soluble substance has such characteristic that it is easily handled and treated at the time or production of recording paper.
  • water-soluble binder examples include hydroxyethyl cellulose, carboxymethyl cellulose, methoxy cellulose, polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylamide, polyacrylic acid, gelatin and starch.
  • the high molecular electrolyte As a film-forming binder which is water-soluble and electroconductive, there is a high molecular electrolyte.
  • This electrolyte contributes to the increase in electric conductivity of electrorecording paper, and is effectively used for the purpose of lowering the voltage at the time of recording.
  • the high molecular electrolyte includes such cationic and anionic electrolytes as mentioned below.
  • This electrolyte has a functional group of the formula,
  • an organic solvent-soluble binder may also be used.
  • a binary system comprising, for example, a color-forming dye and a coupler
  • the two components should individually be dispersed in the form of fine particles into the binder. If either one of the two components is dissolved in a solvent used to dissolve the binder, a color formation reaction to deprive its function as a recording medium takes place at the time of mixing of the two. Accordingly, solvents for the binder mentioned herein are necessarily limited depending on the kind of color-forming components.
  • water-insoluble binder examples include natural rubber, synthetic rubbers, chlorinated rubbers, alkyd resins, styrene-butadiene copolymers, polybutyl methacrylate, low molecular weight ethylene polymers, low molecular weight styrene polymers, polyvinyl butyral, phenolic resins and nitrocellulose.
  • Examples 1 to 6 show recording papers of the structure shown in FIG. 1.
  • EXAMPLE 1 100 Parts by weight of a toluene solution of a styrene-butadiene copolymer (styrenezbutadiene 85:15) was mixed with 25 parts by weight of ferric stearate, and the resulting mixture was pulverized in a 500 ml.
  • the ferric stearate had scarcely dissolved and had dispersed in the form of fine particles of less than 5 microns.
  • the aforesaid liquids A and B were mixed with each other in a weight ratio of 1:1 to pre pare a liquid E.
  • the liquid E was mixed with 100 parts by weight of the aforesaid liquid C, and the resulting mixture was coated on a white paper in the same manner as mentioned previously to obtain a recording paper.
  • This recording paper was subjected to recording under the same conditions as mentioned above.
  • the relation between the amount of the liquid E per 100 parts by weight of the liquid C, the surface resistivity of the recording paper, and the reflective density of the recorded image formed on the recording paper was as shown in the following table:
  • a mixture comprising 100 parts by weight of titanium dioxide and 100 parts by weight of acetone was pulverized in a 500 ml. ball mill for 24 hours, filtered and then dried to obtain a fine titanium dioxide powder of less than 5 microns in particle size.
  • a vapor of aluminum was deposited by vacuum evaporation under 3 X 10 torr with shaking, whereby a fine titanium dioxide powder having an aluminum coating was obtained.
  • the specific resistance of this titanium dioxide powder was 5 cm.
  • 100 Parts by weight of the fine titanium dioxide powder, 30 parts by weight of the liquid A used in Example 1, 30 parts by weight of the liquid B used in Example 1, and 100 parts by weight of a toluene solution of a styrene-butadiene copolymer were mixed together with stirring.
  • the resulting mixed liquid was coated to a thickness of 15 microns on a white paper having a thickness of 60 microns, and was then dried to obtain a recording paper.
  • the thus obtained recording paper was pale graycolored and had a surface resistivity of 2.8 X (I.
  • This recording paper was subjected to recording under the same conditions as in Example 1, whereby a recorded image having a reflective density of D 0.82 was obtained.
  • EXAMPLE 3 100 Parts by weight of cuprous iodide was mixed with 100 parts by weight of a 5 aqueous solution of polyvinyl alcohol (PVA205"produced by Kuraray Co.), and the resulting mixture was pulverized in a 500 ml. ball mill for 48 hours to prepare a dispersion (liquid A).
  • PVA205 polyvinyl alcohol
  • liquid D 10 parts by weight of the liquid B and 100 parts by weight of the liquid C were stirred and mixed together by means of a mixer to prepare a liquid D.
  • the color-forming dye and the coupler had individually dispersed in the form of fine particles, and it may be said that there was no direct contact between the two particles.
  • This recording paper was subjected to recording in the manner as shown in F IG. 2, using as the recording needle electrode 3 a tungsten wire of 0.25 mm. in diameter and running the wire at a rate of 540 mm/sec. while applying an alternating current voltage of 300 V., whereby a brilliant blue record having a reflective density of 0.86 was obtained.
  • EXAMPLE 4 60 Parts by weight of the liquid D used in Example 3, 100 parts by weight of the fine silica gel powder coated with a Nesa (SnO, transparent film which was stated in item (d) of the paragraph Electroconductive substance and parts by weight of a 5 aqueous polyvinyl alcohol solution were mixed together by means of a mixer. The resulting mixture was coated on a white paper so as to form a film having a dry thickness of 15 microns, and was then dried to obtain an electrorecording paper. The surface resistivity of the thus obtained recording paper was 2.5 X 10' 0. This recording paper was subjected to recording in the manner shown in FIG. 2 while applying an alternating current voltage of 1.5 KV., whereby a blue recorded image having a reflective density of D 0.67 was obtained.
  • EXAMPLE 5 100 Parts by weight of cuprous iodide, l0 parts by weight of Luecomethylene Blue, and parts by weight of a l aqueous gelatin solution were mixed together, and the resulting mixture was pulverized in a ball mill for 24 hours to prepare a dispersion. This dispersion was coated on a white paper and then dried to obtain a white recording paper. An electric current was applied to the thus obtained recording paper, whereby a pale blue record was obtained.
  • EXAMPLE 6 100 Parts by weight of antimony-diffused tin dioxide, 10 parts by weight of Leucomethylene Blue, and 130 parts by weight of a l aqueous gelatin solution were mixed together, and the resulting mixture was pulverized in a ball mill for 24 hours to. prepare a dispersion. This dispersion was coated on a white paper so as to form a film having a thickness of 15 microns and was then dried to obtain a pale blue recording paper. An electric current was applied to the thus obtained recording paper, whereby a record having a contrast of 0.32 was obtained.
  • Examples 7 to 10 set forth below illustrate the cases where the electroconductive layers 8 shown in FIGS. 3 and 5 are formed.
  • EXAMPLE 7 This example illustrates a procedure of depositing cuprous iodide directly on a support by vacuum evaporation, in which the curpous iodide used was a first grade commercially available product.
  • EXAMPLE 8 Fine particles of copper were charged into a tungsten basket and were deposited by vacuum evaporation on an art paper under a pressure of 5 X 10 torr in the same manner as in Example 7.
  • the surface resistivity of the copper-deposited paper was 2 to 30.
  • This paper was placed in a desiccator containing fine particles of iodine, and was sucked with an aspirator for 15 to 45 minutes, whereby the copper on the paper surface reacted with the iodine to form cuprous iodide, and the red surface of the paper gradually became white.
  • the suction was further continued, the iodine became excess, and the paper came to be yellowed.
  • the yellowed paper was allowed to stand in air, whereby the excess iodine was gradually released, and the paper became a white paper again.
  • the surface resistivity of the thus obtained paper was 10 to 4 X 10 0.
  • EXAMPLE 9 100 Cubic centimeters of a 4 aqueous solution of polyvinyl alcohol (PVA 205"produced by Kuraray Co.) was mixed with 100 g. of cuprous iodide, and the resulting mixture was pulverized in a 500 ml. ball mill for 24 hours to form a dispersion.
  • This dispersion was coated on an art paper by means of a wire bar, which had been so adjusted as to form a film having a thickness of 15 microns, and was then dried to obtain a coated paper.
  • the surface resistivity of this coated paper was (2 to X 10 .0.
  • coated papers were prepared in the same manner as above.
  • the thus prepared coated papers were substantially identical in surface resistivity with the coated paper obtained in the above.
  • EXAMPLE [0 100 Cubic centimeters of a 10 toluene solution of an 85zl5 copolymer of styrene and butadiene was mixed with 100 g. of cuprous iodide, and the resulting mixture was pulverized in a 500 ml. ball mill for 24 hours to form a dispersion.
  • This dispersion was coated on an art paper by means of a wire bar, which had been so adjusted as to form a film having a thickness of microns, and was then dried to obtain a coated paper.
  • the surface resistivity of this coated paper was (0.5 to 1) x 10" 0.
  • EXAMPLE 1 l A mixture comprising 25 parts by weight of nickel stearate and 100 parts by weight of a 3 aqueous polyacrylamide solution was pulverized in a ball mill to prepare a dispersion (a). On the other hand, a mixture comprising 25 parts by weight of dimethyl glyoxime and I00 parts by weight of a 3 aqueous polyacrylamide solution was pulverized in a ball mill to prepare a dispersion (b). 30 Parts by weight of the dispersion (a), 30 parts by weight of the dispersion (b), 100 parts by weight of a fine silica gel powder coated with a Nesa" film, and 100 parts by weight of a 3 aqueous polyacrylamide solution were mixed together.
  • Example 2 The resulting mixture was coated to a dry film thickness of 8 microns on the electroconductive cuprous iodide layer obtained in Example 1, and was then dried to obtain a pale blue recording paper.
  • This recording paper was subjected to recording under the same conditions as in Example I, while applying an alternating current voltage of 100 V., whereby a pink record having a reflective density of D 0.63 was obtained.
  • EXAMPLE 13 The liquid D of Example 1 was coated on an aluminum-deposited paper so as to form a film having a dry thickness of 10 microns and was then dried to obtain a pale brown recording paper. This recording paper was subjected to recording in the same manner as in Example 1, while applying an alternating current voltage of 40 V., whereby a black record was obtained. When the voltage was increased to 150 V. or more, spark destruction took place to generate fumes as well as to ooze the record.
  • EXAMPLE 14 Parts by weight of amorphous carbon, l0 parts by weight of a low styrene polymer and 100 parts by weight of toluene were mixed together, and the resulting mixture was pulverized in a ball mill for 24 hours to prepare a dispersion. This dispersion was coated on a white paper so as to form a film having a dry thickness of 10 microns, and was then dried to form an electroconductive layer. The surface resistivity of this electroconductive layer was 250 to 500 1.
  • a mixture comprising 10 parts by weight of Leucomalachite Green, 100 parts by weight of silver iodide, 5 parts by weight of sodium polystyrenesulfonate and parts by weight of water was pulverized in a ball mill for 24 hours to prepare a dispersion.
  • This dispersion was coated on the aforesaid electroconductive layer so as to form a film having a dry thickness of 10 microns, and was then dried to obtain a pale yellow recording paper.
  • the thus obtained recording paper was subjected to recording, while applying a direct current voltage of 70 -Continued Example 15 Aqueous polyvinyl C alcohol solution 100 parts by weight Cuprous iodide 100 o.
  • liquids A, B and C were individually pulverized in a ball mill for 24 hours to prepare liquids A, B and C, respectively.
  • 15 Parts by weight of the liquid A, 15 parts by weight of the liquid B and 100 parts by weight of the liquid C were mixed together under stirring by means of a mixer.
  • the resulting mixture was coated to film thickness of microns on an electroconductive paper containing 40 of carbon fibers and having a surface resistivity of 250 Q, and was then dried to obtain a recording paper.
  • This recording paper was subjected to recording while applying a voltage of 100 V., whereby a reddish purple record was obtained.
  • EXAMPLE l6 This example illustrates a recording paper having the structure shown in FIG. 5.
  • Example 12 Between the electroconductive cuprous iodide layer and the color-developing layer containing 3,6- dimethylfuoran and p-hydroxybenzoic acid as colorforrning components, which layers were formed in Example 12, a l:l0 mixture of the liquid A and B prepared in Example l2 was disposed so as to form a film having a thickness of 3 microns to obtain a white recording paper having the color-developing layer 2' shown in FIG. 5. This recording paper was subjected to recording under the same conditions as in Example 12 to give a brilliant red record having a reflective density of D 1.21.
  • An electrorecording paper having a colordeveloping layer containing a component capable of changing color in response to applied heat, said colordeveloping layer comprising a heat coloring component and an electroconductive substance, both of which are dispersed in the form of fine particles in a binder; said electroconductive substance being substantially light reflective, electron conductive and having a specific resistance not greater than 10 Gem and selected from the group consisting of cuprous iodide, tin dioxide, silver-iodide, and antimony; and said colordeveloping layer having a surfacee resistivity of not greater than 10 Born. at a temperature of 20C. and at a relative humidity of 65%; said layer being capable of recording by changing color in response to heat applied by means of an applied electric current.
  • a recording paper according to claim 1, wherein the component capable of being colored by application of heat is composed of a leuco body of a triphenylmethane type dye or a leuco body of a fluoran type dye and a phenolic substance or an organic acid.
  • a recording paper according to claim 1 wherein the component capable of being colored by application of heat is composed of a metal salt and an organic spot reagent, which reacts with metal ions of said salt to form a visually observable reaction product, one of said two substances which is lower in melting point having a melting point of to C.
  • a recording paper according to claim 1, wherein the electroconductive substance is silica gel coated with antimony-containing tin dioxide.
  • a recording paper according to claim 10, wherein the electroconductive layer is a layer composed of a support and a metal, which has been deposited on the support by vacuum evaporation.
  • a recording paper according to claim 12, wherein the electroconductive layer composed of cuprous iodide is a layer comprising a support and cuprous iodide, which has been deposited on the support by vacuum evaporation.
  • a recording paper according to claim 12, wherein the electroconductive layer composed of cuprous iodide is a layer comprising particles of cuprous iodide which have been bonded by use of a binder.
  • a recording paper according to claim 3, wherein the support is an electroconductive material.
  • a recording paper according to claim 3 wherein a second color-developing layer formed by dispersing in a binder fine particles of a component capable of being colored by application of heat is disposed between the color-developing layer and the support.

Landscapes

  • Heat Sensitive Colour Forming Recording (AREA)
  • Color Printing (AREA)
US320820A 1972-04-05 1973-01-03 Electrorecording paper Expired - Lifetime US3875023A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US05/718,989 USRE29427E (en) 1972-04-05 1976-08-30 Electrorecording paper

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP47034762A JPS5133743B2 (de) 1972-04-05 1972-04-05
JP47054666A JPS5133744B2 (de) 1972-05-31 1972-05-31
JP47092644A JPS5116154B2 (de) 1972-09-14 1972-09-14

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US05/718,989 Reissue USRE29427E (en) 1972-04-05 1976-08-30 Electrorecording paper

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US3875023A true US3875023A (en) 1975-04-01

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US320820A Expired - Lifetime US3875023A (en) 1972-04-05 1973-01-03 Electrorecording paper

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US (1) US3875023A (de)
CA (1) CA979215A (de)
DE (1) DE2264107C3 (de)
FR (1) FR2179375A5 (de)
GB (1) GB1422652A (de)
NL (1) NL7217863A (de)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4012292A (en) * 1974-09-25 1977-03-15 Canon Kabushiki Kaisha Image recording member
US4025399A (en) * 1974-04-08 1977-05-24 Canon Kabushiki Kaisha Image recording member
US4082902A (en) * 1973-09-18 1978-04-04 Kabushiki Kaisha Ricoh Spark-recording type printing method and spark-recording material for use thereof
US4199413A (en) * 1977-02-16 1980-04-22 Mita Industrial Company Limited Electric recording material and electric recording process
US4263105A (en) * 1979-08-21 1981-04-21 Issec Sa Electrosensitive recording material and process
SG111098A1 (en) * 2002-02-27 2005-05-30 Lintec Corp Electroconductive paper and carrier for electronic member using said paper

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2528005A (en) * 1948-05-14 1950-10-31 Western Union Telegraph Co Electrosensitive recording blank
US3299433A (en) * 1964-10-21 1967-01-17 Reis electrosbnsitive recording
US3411948A (en) * 1964-04-08 1968-11-19 Hewlett Packard Co Electrosensitive recording medium
US3434878A (en) * 1964-10-26 1969-03-25 Hewlett Packard Co Method of forming a multicolor electrosensitive recording medium and article
US3518038A (en) * 1965-10-20 1970-06-30 Allied Chem Electrographic recording mixture containing a morpholinyl diphenyl methane and 2 triphenyl methane
US3772159A (en) * 1970-12-25 1973-11-13 Jujo Paper Co Ltd Electrical recording medium and process for recording thereon

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2528005A (en) * 1948-05-14 1950-10-31 Western Union Telegraph Co Electrosensitive recording blank
US3411948A (en) * 1964-04-08 1968-11-19 Hewlett Packard Co Electrosensitive recording medium
US3299433A (en) * 1964-10-21 1967-01-17 Reis electrosbnsitive recording
US3434878A (en) * 1964-10-26 1969-03-25 Hewlett Packard Co Method of forming a multicolor electrosensitive recording medium and article
US3518038A (en) * 1965-10-20 1970-06-30 Allied Chem Electrographic recording mixture containing a morpholinyl diphenyl methane and 2 triphenyl methane
US3772159A (en) * 1970-12-25 1973-11-13 Jujo Paper Co Ltd Electrical recording medium and process for recording thereon

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4082902A (en) * 1973-09-18 1978-04-04 Kabushiki Kaisha Ricoh Spark-recording type printing method and spark-recording material for use thereof
US4025399A (en) * 1974-04-08 1977-05-24 Canon Kabushiki Kaisha Image recording member
US4012292A (en) * 1974-09-25 1977-03-15 Canon Kabushiki Kaisha Image recording member
US4199413A (en) * 1977-02-16 1980-04-22 Mita Industrial Company Limited Electric recording material and electric recording process
US4263105A (en) * 1979-08-21 1981-04-21 Issec Sa Electrosensitive recording material and process
SG111098A1 (en) * 2002-02-27 2005-05-30 Lintec Corp Electroconductive paper and carrier for electronic member using said paper

Also Published As

Publication number Publication date
NL7217863A (de) 1973-10-09
GB1422652A (en) 1976-01-28
DE2264107A1 (de) 1973-11-08
FR2179375A5 (de) 1973-11-16
DE2264107C3 (de) 1975-08-28
CA979215A (en) 1975-12-09
DE2264107B2 (de) 1975-01-16

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