US3080254A - Heat-sensitive copying-paper - Google Patents

Heat-sensitive copying-paper Download PDF

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US3080254A
US3080254A US84854959A US3080254A US 3080254 A US3080254 A US 3080254A US 84854959 A US84854959 A US 84854959A US 3080254 A US3080254 A US 3080254A
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heat
copy
sheet
sensitive
atom
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Jr Edwin A Grant
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3M Co
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Minnesota Mining and Manufacturing Co
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/494Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
    • G03C1/498Photothermographic systems, e.g. dry silver
    • G03C1/4989Photothermographic systems, e.g. dry silver characterised by a thermal imaging step, with or without exposure to light, e.g. with a thermal head, using a laser
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/913Material designed to be responsive to temperature, light, moisture
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/165Thermal imaging composition
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/166Toner containing
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31971Of carbohydrate
    • Y10T428/31975Of cellulosic next to another carbohydrate
    • Y10T428/31978Cellulosic next to another cellulosic
    • Y10T428/31982Wood or paper

Definitions

  • This invention is concerned with improvements in heatsensitive copying-paper useful in preparing copies of differentially radiation-absorptive graphic originals, such as printed matter, by thermographic reproduction processes, for example as described in Miller Patent No. 2,740,896. More particularly, the invention concerns improved heatscnsitive copying-papers of the type described in Owen application Serial No. 594,540, tiled lune 28, 1956, now Patent No. 2,910,377, and in which the visible change obtained is a result of an oxidation-reduction reaction involving the liberation of a free metal.
  • a typical heatdsensitive copy-paper of the type just identitied includes in the visibly heatesensitive layer a waterinsoluble silver salt, eg. silver stearato, and an appropriate organic reducing agent, of which 4-methoxy-l-hydroxydihydronaphthalene is representative.
  • a waterinsoluble silver salt eg. silver stearato
  • an appropriate organic reducing agent of which 4-methoxy-l-hydroxydihydronaphthalene is representative.
  • the image areas t-hus formed are sharply outlined and distinctly visible, but normally differ considerably in color and general appearance from the corresponding areas of the printed or typewritten or other graphic original. In other instances the image areas may be yellowish, or greenish, or other less desirable color.
  • Example l A mixture of equimolar proportions of auric behenate and behenic acid is first prepared by precipitation from a mixture of two mols of the water-soluble sodium salt of commercial behenic acid ⁇ and one mol of auric chloride. Five grams of the washed and dried product is intimately dispersed, by prolonged grinding in a ball mill, in a solution of 2 grams of polystyrene resin binder in 93 grams of a mixture of equal parts of acetone and commercial heptane. Separately there is prepared a solution of 3.75 grams of hydroquinone in a solution of 14.5 grams of the styrene resin in 8O grams of the solvent mixture.
  • the dispersion of metal salt and solution of reducing agent are mixed in the ratio of 2 parts of the former to one part of the latter, and a rst portion of the mixture is applied in a thin uniform layer to map overlay tracing paper and dried at room temperature.
  • the resulting sheet is a pale yellow in color. It changes to a reddish purple when placed in momentary contact with a suitably heated metal test bar or when employed in the thermographic reproduction process.
  • Example 2 Silver behenate is prepared by precipitation from an equimolar mixture of silver nitrate and sodium behenate. The water-insoluble salt is washed, dried, and dispersed in a solution of polystyre-ne in methyl ethyl ketone. Hydroquinone is separately dissolved in a solution of polystyrene in a 1:1 mixture of acetone and heptane. Equal quantities of the two products are mixed together to form a mixture having the formula Parts ,by Weight Silver behenate l0 Hydroquinone 4 Binder 12 Volatile liquid vehicle 174 Toning Agent Gm./20 g Sheet Image Color Mixture Color (none) White. Yellow-brown.
  • Example A rnixture of silver behenate and 10% behenic acid is iirst prepared, and 10 parts of the mixture then ball milled with a solution of 4 parts of ethyl cellulose in 86 parts of acetone. Three grams of spiroindane and 4 grams of ethyl cellulose are separately dissolved in 93 grams of acetone. Equal weights of dispersion and solution are mixed together, coated on a thin transparent carrier web at a thickness of two mils, and dried at room temperature.
  • a further coating of a dispersion of 30 parts of zinc oxide and one part of silica gel in a solution of 3 parts of styreneisobutylene copolymer in 66 parts of commercial heptane is applied at 1.5 mils thickness and dried to form a contrasting white opaque protective layer.
  • the sheet yields yellow-brown image areas visible through the transparent carrier when heated in the thermographic process or on the test bar. Copy produced on such sheets is distinct and vlegible ybut lacks esthetic appeal when contrasted lwith the black-on-white typed or printed original.
  • Another copy-sheet is prepared in the same manner except that to the mixture of silver salt dispersion and reducing agent solution there is ii-rst added 2% of phthalazinone. Heat-image areas produced on this sheet are black, and the copy has substantially lthe appearance of the original.
  • Example 4 A copy-sheet prepared as in Example 3 except that gum guaiac is substituted in equal amount for the Spiroindane produces heat-image areas which are yellowish green in color.
  • the incorporation of two percent of phthalazinone (two parts in 16) parts or the coatable liquid mixture) results in the formation or" deep blueblack heat-image m'eas and in much more attractive copies.
  • Example 5 A mix-ture of equal molar amounts of silver behenate and behenic acid is dispersed in a solution of polystyrene resin in a 1:1 mixture of acetone and heptane. Tertiarybutyl catechol is separately dissolved in another portion of the same binder solution. The two compositions are mixed together, a small amount of phthalazirionc is mixed in, and the mixture is coated on paper and dried. rl'he proportions of silver half soap, t-butyl -catechol, and phthalazinone are approximately 50:50zl. The resulting copy-sheet provides black images. In the absence of the phthalazinone the image areas obtained are yellowish brown.
  • Phthalazinone is effective in small amounts, provides a particularly pleasing appearance to the heat-developed image areas without imparting any observable co-lor to the unheated portions, and is a preferred toning agent in my heat-sensitive copy-sheets.
  • Barbituric acid, 2- benzoxazolethiol, and 1-ace-tyl-2-thiohydantoin are fully as effective as phthalazinone.
  • Saccharin is somewhat less effective, and much larger amounts of this material are ⁇ ordinarily required, e.g. as indicated in connection with Example 2.
  • Other examples of toning agents of about the same effectiveness as saccharin include: 5- nitrosaccharin; Z-hydroxybenzthiazole; imidazole; 2-
  • the metal salt is suspended in a volatile vehicle such as methylethyl ketone, Ithe reducing agent is dissolved in the slurry, the mixture is spread over a test sheet, a few small particles or crystals of the compound bein-g tested are sprinkled over a portion of the coating and worked into the slurry with a stirring rod, the coating is permitted to dry, and the sheet is then placed into brief ⁇ contact with a metal test bar at conversion temperature.
  • a volatile vehicle such as methylethyl ketone
  • a solution of about one-half gram of hydroquinone in a slurry of one gram of silver behenate in l0 grams of methylethyl ketone is spread on a strip of white filter paper and powdered phthalazinone is dusted onto half of the coated area and mixed in.
  • the coating dries rapidly.
  • the dusted portion becomes black, whereas the remaining portions turn yellowish brown.
  • the image-forming reaction involves the reduction of a noble metal salt to free metal in an oxidation-reduction reaction.
  • Silver behenate is a preferred salt, being colorless, visibly stable toward light, insoluble in the volatile liquid vehicle, and moisture-resistant.
  • the presence of free behenic acid increases the moisture-resistant properties of the sheet.
  • the salt, with or without the free acid is produced in the desired physical form aad chemical purity without dicul-ty and at reasonable cost.
  • Silver stearato has been successfully substituted for silver behenate, and silver salts of 'many other organic 'acids have also been found useful in these heat-sensitive compositions and copying-papers.
  • a partial list of such organic acids includes oleic, lauric, hydroxystearic, acetic, phthalic, terephthalic, butyric, rn-nit-robenzoic, salicylic, phcnylacetic, pyromellitic, p-phenylbenzoic, undecylenic, camphoric, furoic, acetamidobenzoic and o-aminobenzoic.
  • Reducing agents which have been found useful with such compounds in the formulation of heat-sensitive copy.
  • - sheets include: pyrogallol; 4-azeloyl-'bis-pyrogallol; 4- istearoyl pyrogallol; galloacetophenone; di-tertiary-butyl pyrogallol; gallic acid anilide; methyl gallate, ethyl galllate; normaland iso-propyl gallate; lbutyl gallate; dodecyl gallate; gallic acid; ammonium gallate; ethyl protocatechuate; cetyl protocatechuate; 2,5-dihydroxy benzoic acid, l-hydroxy-Z-naphthoic acid; Z-hydroxy, S-naphthoic acid; phloroglucinol; catechol; 2,3-naphthalene diol; 4- lauroyl catechol; sodium gallate; protocatechualdehyde; 4-methyl esculet
  • These compounds are cyclic or aromatic ⁇ compounds having an active hydrogen atom attached to an atom of carbon, oxygen or nitrogen which in turn is attached to an atom of the cyclic ring. They are capable of causing the reduction of silver ion and precipitation of metallic silver on being dissolved at moderate temperature in la solution of ⁇ aqueous silver nitrate in an organic solvent.
  • the reactant materials are preferably applied to a ⁇ thin exible carrier or backing, such as paper or transparent film, in conjunction with a film-forming polymeric or resinous binder.
  • the binder may itself serve the function of a carrier film; or the reactants may be supported in a fibrous web in the substantial absence of binder. Waxes, fibrous materials, pigments, fillers, dyes, fusible or infusible particulate materials, and various other additives may ⁇ be included for special purposes.
  • the metal salt and organic reducing agent are preferably intermixcd prior to coating, but may be applied in separate but contiguous layers if desired, in which case the toning ,agent is present ⁇ at least in the metal salt layer.
  • the size of the metal particles vaygipearing in the heated image areas of copy-sheets las hereinbefore described is significantly increased by the incorporation of the toning agent in the heat-sensitive layer.
  • the silver particles precipitated from silver nitrate solution by addition of an acetone solution of hydroquinone or the like are found to have a dilferent shape and an increased apparent volume when precipitation occurs in the presence of a toning agent. increase in apparent volume of precipitate may also be observed on addition of small amounts of a toning agent to the silver nitrate-hydroquinone mixture after initial precipitation.
  • silver metal as normally precipitated carries with it adsorbed silver ions; that the toning agents are acidic, or contain labile hydrogen atoms, and permit anion formation; that fusion of one or more of the components of the heat-sensitive coupling permits in effect van ionization of the acidic toning agent along with oxidation-reduction reaction of the maior reactants; that the resulting E anions then neutralize the adsorbed silver ions to permit the growth of particle size', and that the increased size of particles provides for increased internal reliection within the particles, resulting in a darker-appearing image.
  • a heat-sensitive chemically reactive copy-sheet suitable for the preparation from diierentially radiationabsorptive graphic originals of thermographic reproductions having dark-colored image areas of pleasing appearance comprising a thin iiexible carrier web coated with a visibly heat-sensitive coating comprising (l) a lmJforrning binder, (2) a noble metal salt of -an organic acid, an-d (3) a cyclic organic reducing agent for the noble metal ions, having an active hydrogen atom attached to an atom which is selected from the class of oxygen, nitrogen and carbon atoms and is directly attached to an atom of the cyclic ring, and additionally including (4) va significant small proportion, suicient to cause observable darkening of the therrnographic image, of phthalazinone.
  • a heat-sensitive chemically reactive copy-sheet suitable for the preparati-on, from differenti-ally radiationabsorptive graphic originals, of thermographic reproductions having dense black to blue-black image areas said copy-sheet including a visibly heat-sensitive layer comprising a chemically reactive heat-sensitive mixture of a silver salt of an organic acid and an organic reducing agent for the silver ions, and phthalazinone in a small amount suicient to cause observable darkening of the thermographic image.

Description

March 5, 1963 E. A. GRANT, JR 3,080,254
HEAT-SENSITIVE COPYING-PAPER Filed Oct. 26, 1959 70/7//79 age/77'.' 50c/Qing.
Unite Stats 3,080,254 Patented Mar. 5, 1953 This invention is concerned with improvements in heatsensitive copying-paper useful in preparing copies of differentially radiation-absorptive graphic originals, such as printed matter, by thermographic reproduction processes, for example as described in Miller Patent No. 2,740,896. More particularly, the invention concerns improved heatscnsitive copying-papers of the type described in Owen application Serial No. 594,540, tiled lune 28, 1956, now Patent No. 2,910,377, and in which the visible change obtained is a result of an oxidation-reduction reaction involving the liberation of a free metal.
A typical heatdsensitive copy-paper of the type just identitied includes in the visibly heatesensitive layer a waterinsoluble silver salt, eg. silver stearato, and an appropriate organic reducing agent, of which 4-methoxy-l-hydroxydihydronaphthalene is representative. Localized heating of the sheet in the thermographic reproduction pnocess, or, for test purposes, by momentary contact with a metal test bar heated to .a suitable conversion temperaure in the range of about 90-l50 C., causes a visible change to occur in the heat-sensitive layer. The initially white or lightly colored layer is darkened to a brownish appearance at the heated area. The image areas t-hus formed are sharply outlined and distinctly visible, but normally differ considerably in color and general appearance from the corresponding areas of the printed or typewritten or other graphic original. In other instances the image areas may be yellowish, or greenish, or other less desirable color.
It has now been found that the color of the image areas obtained on heating these metal-liberating copy-sheets to conversion temperature may be desirably and leffectively darkened, so that the resulting copy appears in the form of dense black or 'blue-black images on an essentially white background. Copies of typewritten correspondence, printed pages and the like having essentially the appearance of the original are thereby made possible.
The just-described improvement in image appearance is achieved, in accordance with t-he principles of my invention, by including with the metal-liberating heat-sensitive composition a signiiicant small proportion of a heterocyclic organic toning agent containing at least two hetero atoms in the heterocyclic ring, of which at least one is Ia. nitrogen atom.
The following examples and the appended drawing describe specic heatesensitive copy-sheets illustrating the principles of the invention, which however is not to be construed as limited thereto.
Example l A mixture of equimolar proportions of auric behenate and behenic acid is first prepared by precipitation from a mixture of two mols of the water-soluble sodium salt of commercial behenic acid `and one mol of auric chloride. Five grams of the washed and dried product is intimately dispersed, by prolonged grinding in a ball mill, in a solution of 2 grams of polystyrene resin binder in 93 grams of a mixture of equal parts of acetone and commercial heptane. Separately there is prepared a solution of 3.75 grams of hydroquinone in a solution of 14.5 grams of the styrene resin in 8O grams of the solvent mixture. The dispersion of metal salt and solution of reducing agent are mixed in the ratio of 2 parts of the former to one part of the latter, and a rst portion of the mixture is applied in a thin uniform layer to map overlay tracing paper and dried at room temperature. The resulting sheet is a pale yellow in color. It changes to a reddish purple when placed in momentary contact with a suitably heated metal test bar or when employed in the thermographic reproduction process.
To a second portion of the liquid mixture is added 0.1% of phthalazinone. This portion likewise is applied to paper and dried, providing a heat-sensitive copy-paper which converts from pale yellow to deep blue-black when heated as just described.
Example 2 Silver behenate is prepared by precipitation from an equimolar mixture of silver nitrate and sodium behenate. The water-insoluble salt is washed, dried, and dispersed in a solution of polystyre-ne in methyl ethyl ketone. Hydroquinone is separately dissolved in a solution of polystyrene in a 1:1 mixture of acetone and heptane. Equal quantities of the two products are mixed together to form a mixture having the formula Parts ,by Weight Silver behenate l0 Hydroquinone 4 Binder 12 Volatile liquid vehicle 174 Toning Agent Gm./20 g Sheet Image Color Mixture Color (none) White. Yellow-brown.
0.05 ..-do Black. 0.08 ---do Do. Saccharin 0.3 -do Darkbrown-black.
Example A rnixture of silver behenate and 10% behenic acid is iirst prepared, and 10 parts of the mixture then ball milled with a solution of 4 parts of ethyl cellulose in 86 parts of acetone. Three grams of spiroindane and 4 grams of ethyl cellulose are separately dissolved in 93 grams of acetone. Equal weights of dispersion and solution are mixed together, coated on a thin transparent carrier web at a thickness of two mils, and dried at room temperature. A further coating of a dispersion of 30 parts of zinc oxide and one part of silica gel in a solution of 3 parts of styreneisobutylene copolymer in 66 parts of commercial heptane is applied at 1.5 mils thickness and dried to form a contrasting white opaque protective layer. The sheet yields yellow-brown image areas visible through the transparent carrier when heated in the thermographic process or on the test bar. Copy produced on such sheets is distinct and vlegible ybut lacks esthetic appeal when contrasted lwith the black-on-white typed or printed original.
Another copy-sheet is prepared in the same manner except that to the mixture of silver salt dispersion and reducing agent solution there is ii-rst added 2% of phthalazinone. Heat-image areas produced on this sheet are black, and the copy has substantially lthe appearance of the original.
Example 4 A copy-sheet prepared as in Example 3 except that gum guaiac is substituted in equal amount for the Spiroindane produces heat-image areas which are yellowish green in color. The incorporation of two percent of phthalazinone (two parts in 16) parts or the coatable liquid mixture) results in the formation or" deep blueblack heat-image m'eas and in much more attractive copies.
Similarly, the substitution of l,5dihydroxynaphthalene for the spiroindane of Example 3 results in a heat-sensitive copy-sheet which normally provides yellowish brown image areas, but with small amounts of phthaliazinone provides black images.
Example 5 A mix-ture of equal molar amounts of silver behenate and behenic acid is dispersed in a solution of polystyrene resin in a 1:1 mixture of acetone and heptane. Tertiarybutyl catechol is separately dissolved in another portion of the same binder solution. The two compositions are mixed together, a small amount of phthalazirionc is mixed in, and the mixture is coated on paper and dried. rl'he proportions of silver half soap, t-butyl -catechol, and phthalazinone are approximately 50:50zl. The resulting copy-sheet provides black images. In the absence of the phthalazinone the image areas obtained are yellowish brown.
Phthalazinone is effective in small amounts, provides a particularly pleasing appearance to the heat-developed image areas without imparting any observable co-lor to the unheated portions, and is a preferred toning agent in my heat-sensitive copy-sheets. Barbituric acid, 2- benzoxazolethiol, and 1-ace-tyl-2-thiohydantoin are fully as effective as phthalazinone. Saccharin is somewhat less effective, and much larger amounts of this material are `ordinarily required, e.g. as indicated in connection with Example 2. Other examples of toning agents of about the same effectiveness as saccharin include: 5- nitrosaccharin; Z-hydroxybenzthiazole; imidazole; 2-
thiazole; and l\T,N-ethylenethiourea.
The effectiveness of the toning action obtained with these and other equivalent nitrogen-containing heterocyclic toning agents will vary with the particular toning agent and the amount thereof, and with the specific natu-re of the noble metal salt and the organic reducing agent, and with other factors. A test procedure is available, however, by means of which effective toning agents may be selected for any speelt-led composition. in this test, the metal salt is suspended in a volatile vehicle such as methylethyl ketone, Ithe reducing agent is dissolved in the slurry, the mixture is spread over a test sheet, a few small particles or crystals of the compound bein-g tested are sprinkled over a portion of the coating and worked into the slurry with a stirring rod, the coating is permitted to dry, and the sheet is then placed into brief` contact with a metal test bar at conversion temperature. For example, a solution of about one-half gram of hydroquinone in a slurry of one gram of silver behenate in l0 grams of methylethyl ketone is spread on a strip of white filter paper and powdered phthalazinone is dusted onto half of the coated area and mixed in. The coating dries rapidly. When placed on a metal rod heated to 120 C., the dusted portion becomes black, whereas the remaining portions turn yellowish brown. With compounds which have no toning action, no observable difference in color is obtained between the two areas of the test strip.
The image-forming reaction involves the reduction of a noble metal salt to free metal in an oxidation-reduction reaction. Silver behenate is a preferred salt, being colorless, visibly stable toward light, insoluble in the volatile liquid vehicle, and moisture-resistant. The presence of free behenic acid increases the moisture-resistant properties of the sheet. The salt, with or without the free acid, is produced in the desired physical form aad chemical purity without dicul-ty and at reasonable cost. Silver stearato has been successfully substituted for silver behenate, and silver salts of 'many other organic 'acids have also been found useful in these heat-sensitive compositions and copying-papers. A partial list of such organic acids includes oleic, lauric, hydroxystearic, acetic, phthalic, terephthalic, butyric, rn-nit-robenzoic, salicylic, phcnylacetic, pyromellitic, p-phenylbenzoic, undecylenic, camphoric, furoic, acetamidobenzoic and o-aminobenzoic.
Reducing agents which have been found useful with such compounds in the formulation of heat-sensitive copy.- sheets include: pyrogallol; 4-azeloyl-'bis-pyrogallol; 4- istearoyl pyrogallol; galloacetophenone; di-tertiary-butyl pyrogallol; gallic acid anilide; methyl gallate, ethyl galllate; normaland iso-propyl gallate; lbutyl gallate; dodecyl gallate; gallic acid; ammonium gallate; ethyl protocatechuate; cetyl protocatechuate; 2,5-dihydroxy benzoic acid, l-hydroxy-Z-naphthoic acid; Z-hydroxy, S-naphthoic acid; phloroglucinol; catechol; 2,3-naphthalene diol; 4- lauroyl catechol; sodium gallate; protocatechualdehyde; 4-methyl esculetin; 3,4-dihydroxy henzoic acid; 2,3-dihydroxy benzoic acid; hydroquinone; 4,4'-dihydroxy biphenyl; 3,4-dihydroxyphenylacetic acid; 4(3',4-dihydroxy phenylazo)benzoic acid; 2,2methylene `bis-3,4,5-trihydroxybenzoic acid; orthoand pana-phenylene diamine; tetramethyl benzidine; 4,4',4diethylamino triphenylmethane; o, m, and p-aminobenzoic acids; alpha and beta naphthols; 4-methoxy, l-hydroxy-dihydronaphthalene; and tetrahydroquinoline. These compounds are cyclic or aromatic `compounds having an active hydrogen atom attached to an atom of carbon, oxygen or nitrogen which in turn is attached to an atom of the cyclic ring. They are capable of causing the reduction of silver ion and precipitation of metallic silver on being dissolved at moderate temperature in la solution of `aqueous silver nitrate in an organic solvent.
The reactant materials are preferably applied to a` thin exible carrier or backing, such as paper or transparent film, in conjunction with a film-forming polymeric or resinous binder. In somewhat larger amounts the binder may itself serve the function of a carrier film; or the reactants may be supported in a fibrous web in the substantial absence of binder. Waxes, fibrous materials, pigments, fillers, dyes, fusible or infusible particulate materials, and various other additives may `be included for special purposes. The metal salt and organic reducing agent are preferably intermixcd prior to coating, but may be applied in separate but contiguous layers if desired, in which case the toning ,agent is present `at least in the metal salt layer.
By means of the electron microscope it has been observed that the size of the metal particles vaygipearing in the heated image areas of copy-sheets las hereinbefore described is significantly increased by the incorporation of the toning agent in the heat-sensitive layer. Again, the silver particles precipitated from silver nitrate solution by addition of an acetone solution of hydroquinone or the like are found to have a dilferent shape and an increased apparent volume when precipitation occurs in the presence of a toning agent. increase in apparent volume of precipitate may also be observed on addition of small amounts of a toning agent to the silver nitrate-hydroquinone mixture after initial precipitation. In possible explanation of these effects as well as of the toning effect generally, it is suggested that silver metal as normally precipitated carries with it adsorbed silver ions; that the toning agents are acidic, or contain labile hydrogen atoms, and permit anion formation; that fusion of one or more of the components of the heat-sensitive coupling permits in effect van ionization of the acidic toning agent along with oxidation-reduction reaction of the maior reactants; that the resulting E anions then neutralize the adsorbed silver ions to permit the growth of particle size', and that the increased size of particles provides for increased internal reliection within the particles, resulting in a darker-appearing image. But regardless of theory, it has been shown that darker and more pleasing image-forming areas are obtainable by incorporation, in heat-sensitive copy-sheets employing metalliberating oxidation-reduction reaction com-positions, of heterocyclic organic toning agents containing at least two hetero atoms of which at least one is a nitrogen atom.
What I claim is as follows:
1. A heat-sensitive chemically reactive copy-sheet suitable for the preparation from diierentially radiationabsorptive graphic originals of thermographic reproductions having dark-colored image areas of pleasing appearance, said copy-sheet comprising a thin iiexible carrier web coated with a visibly heat-sensitive coating comprising (l) a lmJforrning binder, (2) a noble metal salt of -an organic acid, an-d (3) a cyclic organic reducing agent for the noble metal ions, having an active hydrogen atom attached to an atom which is selected from the class of oxygen, nitrogen and carbon atoms and is directly attached to an atom of the cyclic ring, and additionally including (4) va significant small proportion, suicient to cause observable darkening of the therrnographic image, of phthalazinone.
2. A heat-sensitive chemically reactive copy-sheet suitable for the preparati-on, from differenti-ally radiationabsorptive graphic originals, of thermographic reproductions having dense black to blue-black image areas, said copy-sheet including a visibly heat-sensitive layer comprising a chemically reactive heat-sensitive mixture of a silver salt of an organic acid and an organic reducing agent for the silver ions, and phthalazinone in a small amount suicient to cause observable darkening of the thermographic image.
References Cited in the file of this patent UNITED STATES PATENTS 2,514,650 Knott et al. July l1, 1950 2,699,393 Weyde r Ian. 11, 1955 2,910,377 Owen Oct. 27, 1959

Claims (1)

1. A HEAT-SENSITIVE CHEMICALLY REACTIVE COPY-SHEET SUITABLE FOR THE PREPARATION FROM DIFFERENTLY RADIATIONABSORPTIVE GRAPHIC ORIGINALS OF THERMOGRAPHIC REPRODUCTIONS HAVING DARK-COLORED IMAGE AREAS OF PLEASING APPEARANCE, SAID COPY-SHEET COMPRISING A THIN FLEXIBLE CARRIER WEB COATED WITH A VISIBLY HEAT-SENSITIVE COATING COMPRISING (1) A FILM-FORMING BINDER, (2) A NOBLE METAL SALT OF AN ORGANIC ACID, AND (3) A CYCLIC ORGANIC REDUCING AGENT FOR THE NOBLE METAL IRONS, HAVING AN ACTIVE HYDROGEN ATOM ATTACHED TO AN ATOM WHICH IS SELECTED FROM THE CLASS OF OXYGEN, NITROGEN AND CARBON ATOMS AND IS DIRECTLY ATTACHED TO AN ATOM OF THE CYCLIC RING, AND ADDITIONALLY INCLUDING (4) A SIGNIFICANT SMALL PROPORTION, SUFFICIENT TO CAUSE OBSERVABLE DARKENING OF THE THERMOGRAPHIC IMAGE OF PHTHALAZINONE.
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Cited By (84)

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US3260613A (en) * 1963-03-15 1966-07-12 Interchem Corp Heat-sensitive sheet for thermographic copying
US3342618A (en) * 1962-12-31 1967-09-19 Ibm Thermographic copying material
US3446648A (en) * 1965-09-27 1969-05-27 Minnesota Mining & Mfg Reactive copying sheet and method of using
US3455687A (en) * 1964-11-28 1969-07-15 Eastman Kodak Co Photothermographic copying process
US3515559A (en) * 1966-09-30 1970-06-02 Minnesota Mining & Mfg Dry process proof sheet composition
US3816139A (en) * 1970-04-13 1974-06-11 Nashua Corp Thermographic copy sheet containing phthalimide
US3839041A (en) * 1970-06-03 1974-10-01 Eastman Kodak Co Stabilizer precursors in photothermographic elements and compositions
US3844797A (en) * 1972-04-27 1974-10-29 Agfa Gevaert Photosensitive recording material
US3847612A (en) * 1973-02-02 1974-11-12 Minnesota Mining & Mfg Light-sensitive heat-developable sheet material
US3885967A (en) * 1973-05-07 1975-05-27 Fuji Photo Film Co Ltd Thermally developable light-sensitive element
US4013473A (en) * 1974-08-24 1977-03-22 Agfa-Gevaert N.V. Recording materials and image receiving materials for producing copies in a dry way
US4076534A (en) * 1973-10-16 1978-02-28 Fuji Photo Film Co., Ltd. Heat developable light-sensitive material
US4268626A (en) * 1978-08-28 1981-05-19 Asahi Kasei Kogyo Kabushiki Kaisha Dry image forming material
US4349623A (en) * 1979-06-15 1982-09-14 Fuji Photo Film Co., Ltd. Silver halide photographic materials
US4379835A (en) * 1980-12-22 1983-04-12 Minnesota Mining And Manufacturing Company Black image from a thermographic imaging system
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US4585734A (en) * 1985-02-01 1986-04-29 Minnesota Mining And Manufacturing Company Photothermographic toners
US4741992A (en) * 1986-09-22 1988-05-03 Eastman Kodak Company Thermally processable element comprising an overcoat layer containing poly(silicic acid)
US4828971A (en) * 1988-03-24 1989-05-09 Eastman Kodak Company Thermally processable element comprising a backing layer
US4886739A (en) * 1988-08-10 1989-12-12 Eastman Kodak Company Thermally processable imaging element and process
US4942115A (en) * 1989-04-24 1990-07-17 Eastman Kodak Company Thermally processable imaging element comprising an overcoat layer
US5275932A (en) * 1992-03-16 1994-01-04 Minnesota Mining And Manufacturing Company Thermal development accelerators for thermographic materials
US5424182A (en) * 1993-01-15 1995-06-13 Labelon Corporation Aqueous coating composition for thermal imaging film
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US5482814A (en) * 1993-07-15 1996-01-09 Canon Kabushiki Kaisha Thermal developing photosensitive member and image forming method using the thermal developing photosensitive member
EP0692391A1 (en) 1994-07-13 1996-01-17 Agfa-Gevaert N.V. Heat-sensitive recording material
EP0692733A2 (en) * 1994-07-07 1996-01-17 Agfa-Gevaert N.V. Direct thermal recording process
US5492805A (en) * 1994-06-30 1996-02-20 Minnesota Mining And Manufacturing Company Blocked leuco dyes for photothermographic elements
US5492804A (en) * 1994-06-30 1996-02-20 Minnesota Mining And Manufacturing Company Chromogenic leuco redox-dye-releasing compounds for photothermographic elements
US5492803A (en) * 1995-01-06 1996-02-20 Minnesota Mining And Manufacturing Company Hydrazide redox-dye-releasing compounds for photothermographic elements
EP0713135A2 (en) 1994-11-21 1996-05-22 Eastman Kodak Company Imaging element comprising an electrically-conductive layer containing antimony-doped tin oxide particles
US5527758A (en) * 1994-06-15 1996-06-18 Agfa-Gevaert N.V. Direct thermal imaging process with improved tone reproduction
US5529889A (en) * 1992-03-02 1996-06-25 Canon Kabushiki Kaisha Heat developable photosensitive material and image forming method which uses the same
US5541055A (en) * 1993-09-28 1996-07-30 Canon Kabushiki Kaisha Heat developing photosensitive material and image formed by using the same
US5547831A (en) * 1992-11-18 1996-08-20 Canon Kabushiki Kaisha Dry process silver salt photosensitive material and image forming method making use of this dry process silver salt photosensitive material
EP0775595A1 (en) 1995-11-27 1997-05-28 Agfa-Gevaert N.V. Thermographic recording material with phosphoric acid and derivative as lubricant
EP0775592A1 (en) 1995-11-27 1997-05-28 Agfa-Gevaert N.V. Thermal image-forming process
EP0779539A1 (en) 1995-11-27 1997-06-18 Agfa-Gevaert N.V. Thermographic material with outermost organic antistatic layer
EP0782043A1 (en) 1995-12-27 1997-07-02 Agfa-Gevaert N.V. Thermographic recording material which improved tone reproduction
EP0785464A1 (en) 1996-01-18 1997-07-23 Eastman Kodak Company Imaging element having an electrically-conductive layer
US5750319A (en) * 1996-05-21 1998-05-12 Agfa-Gevaert Substantially non-photosensitive thermographic recording material with improved stability and image-tone
US5759752A (en) * 1993-03-08 1998-06-02 Agfa-Gevaert N.V. Direct thermal imaging material containing a protective layer
EP0845709A1 (en) 1996-11-29 1998-06-03 Agfa-Gevaert N.V. A heat sensitive imaging element and a method for producing lithographic plates therewith
US5783380A (en) * 1996-09-24 1998-07-21 Eastman Kodak Company Thermally processable imaging element
US5804365A (en) * 1997-03-07 1998-09-08 Eastman Kodak Company Thermally processable imaging element having a crosslinked hydrophobic binder
US5863859A (en) * 1994-05-30 1999-01-26 Agfa-Gevaert N.V. Heat-sensitive material suited for use in direct thermal recording
US5891610A (en) * 1996-11-22 1999-04-06 Eastman Kodak Company Thermally processable imaging element with improved adhesion of the overcoat layer
US5891615A (en) * 1997-04-08 1999-04-06 Imation Corp. Chemical sensitization of photothermographic silver halide emulsions
US5928857A (en) * 1994-11-16 1999-07-27 Minnesota Mining And Manufacturing Company Photothermographic element with improved adherence between layers
US5939249A (en) * 1997-06-24 1999-08-17 Imation Corp. Photothermographic element with iridium and copper doped silver halide grains
US5981156A (en) * 1997-08-20 1999-11-09 Eastman Kodak Company Thermally processable imaging element
US5989796A (en) * 1998-09-30 1999-11-23 Eastman Kodak Company Organic silver salt containing thermally processable elements with spot reducing surfactant combinations
US6020117A (en) * 1998-09-30 2000-02-01 Eastman Kodak Company Thermally processable imaging element
US6033839A (en) * 1998-05-20 2000-03-07 Eastman Kodak Company Polymeric matte particles
US6090747A (en) * 1996-12-17 2000-07-18 Labelon Corporation Thermosensitive direct image-recording material
US6117624A (en) * 1993-06-04 2000-09-12 Eastman Kodak Company Infrared sensitized, photothermographic article
US6146822A (en) * 1997-06-06 2000-11-14 Fuji Photo Film Co., Ltd. Thermographic or photothermographic image recording elements
US6171707B1 (en) 1994-01-18 2001-01-09 3M Innovative Properties Company Polymeric film base having a coating layer of organic solvent based polymer with a fluorinated antistatic agent
US6225038B1 (en) 1999-11-04 2001-05-01 Eastman Kodak Company Thermally processable imaging element
US6280923B1 (en) 1995-07-18 2001-08-28 Agfa-Gevaert Photothermographic recording material
US6340985B1 (en) 1997-12-10 2002-01-22 Fuji Photo Film Co. Ltd. Thermal recording apparatus
US6348308B1 (en) 1997-09-03 2002-02-19 Agfa-Gevaert Substantially light-insensitive thermographic recording material with improved stability and image-tone
US6524000B1 (en) 1999-04-30 2003-02-25 Ncr Corporation Time-temperature indicators activated with direct thermal printing and methods for their production
US6599685B1 (en) 2002-01-08 2003-07-29 Eastman Kodak Company Thermally developable imaging materials having improved shelf stability and stabilizing compositions
US6608002B1 (en) 1996-09-23 2003-08-19 Media Solutions International, Inc. Direct thermal printable film with friction-reducing layer
US6630291B1 (en) 2002-08-21 2003-10-07 Eastman Kodak Company Thermally sensitive imaging materials containing phthalazine precursor
US6677274B2 (en) 2000-05-25 2004-01-13 Agfa-Gevaert Thermographic recording material with improved image tone
US20040152027A1 (en) * 2002-12-19 2004-08-05 Agfa-Gevaert Toning agents for use in thermographic recording materials
US20040198602A1 (en) * 2003-04-07 2004-10-07 Eastman Kodak Company Thermographic materials containing metal oxide conductive layers
US20050186520A1 (en) * 2004-02-25 2005-08-25 Eastman Kodak Company Silver-free black-and-white thermographic materials
US20050186518A1 (en) * 2004-02-25 2005-08-25 Eastman Kodak Company Silver-free black-and-white thermographic materials containing a benzoquinone and methods of imaging
US20050186521A1 (en) * 2004-02-25 2005-08-25 Eastman Kodak Company Black-and-white thermographic materials with improved image tone
US20060100103A1 (en) * 2004-11-05 2006-05-11 Agfa-Gevaert Toning agents for use in thermographic recording materials
US20060100102A1 (en) * 2004-11-05 2006-05-11 Agfa-Gevaert Toning agents for use in thermographic recording materials
US7045487B2 (en) 2002-12-19 2006-05-16 Agfa Gevaert Toning agents for use in substantially light-insensitive recording materials
US7468241B1 (en) 2007-09-21 2008-12-23 Carestream Health, Inc. Processing latitude stabilizers for photothermographic materials
US20090081578A1 (en) * 2007-09-21 2009-03-26 Carestream Health, Inc. Method of preparing silver carboxylate soaps
EP2042871A1 (en) 2007-09-28 2009-04-01 Fujifilm Corporation Method for mixing two or more types of liquids in porous carrier
EP2065706A2 (en) 2007-11-29 2009-06-03 Fujifilm Corporation A measurement kit and an immunochromatography method
US20090181332A1 (en) * 2008-01-14 2009-07-16 William Donald Ramsden Protective overcoats for thermally developable materials
WO2015148028A1 (en) 2014-03-24 2015-10-01 Carestream Health, Inc. Thermally developable imaging materials
WO2016073086A1 (en) 2014-11-04 2016-05-12 Carestream Health, Inc. Image forming materials, preparations, and compositions
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Cited By (101)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3342618A (en) * 1962-12-31 1967-09-19 Ibm Thermographic copying material
US3260613A (en) * 1963-03-15 1966-07-12 Interchem Corp Heat-sensitive sheet for thermographic copying
US3455687A (en) * 1964-11-28 1969-07-15 Eastman Kodak Co Photothermographic copying process
US3446648A (en) * 1965-09-27 1969-05-27 Minnesota Mining & Mfg Reactive copying sheet and method of using
US3515559A (en) * 1966-09-30 1970-06-02 Minnesota Mining & Mfg Dry process proof sheet composition
US3816139A (en) * 1970-04-13 1974-06-11 Nashua Corp Thermographic copy sheet containing phthalimide
US3839041A (en) * 1970-06-03 1974-10-01 Eastman Kodak Co Stabilizer precursors in photothermographic elements and compositions
US3844797A (en) * 1972-04-27 1974-10-29 Agfa Gevaert Photosensitive recording material
US3847612A (en) * 1973-02-02 1974-11-12 Minnesota Mining & Mfg Light-sensitive heat-developable sheet material
US3885967A (en) * 1973-05-07 1975-05-27 Fuji Photo Film Co Ltd Thermally developable light-sensitive element
US4076534A (en) * 1973-10-16 1978-02-28 Fuji Photo Film Co., Ltd. Heat developable light-sensitive material
US4013473A (en) * 1974-08-24 1977-03-22 Agfa-Gevaert N.V. Recording materials and image receiving materials for producing copies in a dry way
US4268626A (en) * 1978-08-28 1981-05-19 Asahi Kasei Kogyo Kabushiki Kaisha Dry image forming material
US4349623A (en) * 1979-06-15 1982-09-14 Fuji Photo Film Co., Ltd. Silver halide photographic materials
US4379835A (en) * 1980-12-22 1983-04-12 Minnesota Mining And Manufacturing Company Black image from a thermographic imaging system
FR2530191A1 (en) * 1982-07-16 1984-01-20 Aussedat Rey NOVEL SACCHARIN-BASED COLOR DEVELOPERS AND / OR SACCHARIN DERIVATIVES, THERMOGRAPHIC RECORDING COMPOSITIONS CONTAINING THEM AND CORRESPONDING MEDIA
EP0106772A1 (en) * 1982-07-16 1984-04-25 Aussedat-Rey Thermographic compositions containing these developers and thermographic copying materials
US4536219A (en) * 1982-07-16 1985-08-20 Societe Anonyme: Aussedat-Rey Thermographic recording compositions
US4585734A (en) * 1985-02-01 1986-04-29 Minnesota Mining And Manufacturing Company Photothermographic toners
US4741992A (en) * 1986-09-22 1988-05-03 Eastman Kodak Company Thermally processable element comprising an overcoat layer containing poly(silicic acid)
US4828971A (en) * 1988-03-24 1989-05-09 Eastman Kodak Company Thermally processable element comprising a backing layer
US4886739A (en) * 1988-08-10 1989-12-12 Eastman Kodak Company Thermally processable imaging element and process
US4942115A (en) * 1989-04-24 1990-07-17 Eastman Kodak Company Thermally processable imaging element comprising an overcoat layer
US5529889A (en) * 1992-03-02 1996-06-25 Canon Kabushiki Kaisha Heat developable photosensitive material and image forming method which uses the same
US5275932A (en) * 1992-03-16 1994-01-04 Minnesota Mining And Manufacturing Company Thermal development accelerators for thermographic materials
US5547831A (en) * 1992-11-18 1996-08-20 Canon Kabushiki Kaisha Dry process silver salt photosensitive material and image forming method making use of this dry process silver salt photosensitive material
US5424182A (en) * 1993-01-15 1995-06-13 Labelon Corporation Aqueous coating composition for thermal imaging film
US5759752A (en) * 1993-03-08 1998-06-02 Agfa-Gevaert N.V. Direct thermal imaging material containing a protective layer
US6117624A (en) * 1993-06-04 2000-09-12 Eastman Kodak Company Infrared sensitized, photothermographic article
US5482814A (en) * 1993-07-15 1996-01-09 Canon Kabushiki Kaisha Thermal developing photosensitive member and image forming method using the thermal developing photosensitive member
US5541055A (en) * 1993-09-28 1996-07-30 Canon Kabushiki Kaisha Heat developing photosensitive material and image formed by using the same
EP0663301A1 (en) * 1994-01-14 1995-07-19 Agfa-Gevaert N.V. Recording material for a direct thermal imaging process
US6171707B1 (en) 1994-01-18 2001-01-09 3M Innovative Properties Company Polymeric film base having a coating layer of organic solvent based polymer with a fluorinated antistatic agent
US5863859A (en) * 1994-05-30 1999-01-26 Agfa-Gevaert N.V. Heat-sensitive material suited for use in direct thermal recording
US5527758A (en) * 1994-06-15 1996-06-18 Agfa-Gevaert N.V. Direct thermal imaging process with improved tone reproduction
US5705676A (en) * 1994-06-30 1998-01-06 Minnesota Mining And Manufacturing Company Chromogenic leuco redox-dye-releasing compounds for photothermographic elements
US5696289A (en) * 1994-06-30 1997-12-09 Minnesota Mining And Manufacturing Company Blocked leuco dyes for photothermographic elements
US5492805A (en) * 1994-06-30 1996-02-20 Minnesota Mining And Manufacturing Company Blocked leuco dyes for photothermographic elements
US5492804A (en) * 1994-06-30 1996-02-20 Minnesota Mining And Manufacturing Company Chromogenic leuco redox-dye-releasing compounds for photothermographic elements
EP0692733A2 (en) * 1994-07-07 1996-01-17 Agfa-Gevaert N.V. Direct thermal recording process
EP0692733A3 (en) * 1994-07-07 1996-03-20 Agfa Gevaert Nv Direct thermal recording process
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US5928857A (en) * 1994-11-16 1999-07-27 Minnesota Mining And Manufacturing Company Photothermographic element with improved adherence between layers
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US5492803A (en) * 1995-01-06 1996-02-20 Minnesota Mining And Manufacturing Company Hydrazide redox-dye-releasing compounds for photothermographic elements
US6280923B1 (en) 1995-07-18 2001-08-28 Agfa-Gevaert Photothermographic recording material
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EP0775595A1 (en) 1995-11-27 1997-05-28 Agfa-Gevaert N.V. Thermographic recording material with phosphoric acid and derivative as lubricant
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US5750319A (en) * 1996-05-21 1998-05-12 Agfa-Gevaert Substantially non-photosensitive thermographic recording material with improved stability and image-tone
US6608002B1 (en) 1996-09-23 2003-08-19 Media Solutions International, Inc. Direct thermal printable film with friction-reducing layer
US20030203818A1 (en) * 1996-09-23 2003-10-30 Media Solutions International, Inc. Direct thermal printable film and laminate
US5783380A (en) * 1996-09-24 1998-07-21 Eastman Kodak Company Thermally processable imaging element
US5891610A (en) * 1996-11-22 1999-04-06 Eastman Kodak Company Thermally processable imaging element with improved adhesion of the overcoat layer
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US6090747A (en) * 1996-12-17 2000-07-18 Labelon Corporation Thermosensitive direct image-recording material
US5804365A (en) * 1997-03-07 1998-09-08 Eastman Kodak Company Thermally processable imaging element having a crosslinked hydrophobic binder
US5891615A (en) * 1997-04-08 1999-04-06 Imation Corp. Chemical sensitization of photothermographic silver halide emulsions
US6146822A (en) * 1997-06-06 2000-11-14 Fuji Photo Film Co., Ltd. Thermographic or photothermographic image recording elements
US6060231A (en) * 1997-06-24 2000-05-09 Eastman Kodak Company Photothermographic element with iridium and copper doped silver halide grains
US5939249A (en) * 1997-06-24 1999-08-17 Imation Corp. Photothermographic element with iridium and copper doped silver halide grains
US5981156A (en) * 1997-08-20 1999-11-09 Eastman Kodak Company Thermally processable imaging element
US6348308B1 (en) 1997-09-03 2002-02-19 Agfa-Gevaert Substantially light-insensitive thermographic recording material with improved stability and image-tone
US6340985B1 (en) 1997-12-10 2002-01-22 Fuji Photo Film Co. Ltd. Thermal recording apparatus
US6033839A (en) * 1998-05-20 2000-03-07 Eastman Kodak Company Polymeric matte particles
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