EP0669875A1 - Direct thermal imaging material. - Google Patents

Direct thermal imaging material.

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Publication number
EP0669875A1
EP0669875A1 EP93924602A EP93924602A EP0669875A1 EP 0669875 A1 EP0669875 A1 EP 0669875A1 EP 93924602 A EP93924602 A EP 93924602A EP 93924602 A EP93924602 A EP 93924602A EP 0669875 A1 EP0669875 A1 EP 0669875A1
Authority
EP
European Patent Office
Prior art keywords
recording material
protective layer
heat sensitive
binder
present
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP93924602A
Other languages
German (de)
French (fr)
Other versions
EP0669875B1 (en
Inventor
Bartholomeus Cyriel Horsten
Carlo Alfons Uyttendaele
Guy Denis Anna Jansen
Ronald Schuerwegen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Agfa Gevaert NV
Original Assignee
Agfa Gevaert NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from EP93202599A external-priority patent/EP0641669B1/en
Application filed by Agfa Gevaert NV filed Critical Agfa Gevaert NV
Priority to EP93924602A priority Critical patent/EP0669875B1/en
Priority claimed from PCT/EP1993/003120 external-priority patent/WO1994011198A1/en
Publication of EP0669875A1 publication Critical patent/EP0669875A1/en
Application granted granted Critical
Publication of EP0669875B1 publication Critical patent/EP0669875B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/46—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography characterised by the light-to-heat converting means; characterised by the heat or radiation filtering or absorbing means or layers
    • B41M5/465—Infrared radiation-absorbing materials, e.g. dyes, metals, silicates, C black
    • 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
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42—Intermediate, backcoat, or covering layers
    • 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
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42—Intermediate, backcoat, or covering layers
    • B41M5/423—Intermediate, backcoat, or covering layers characterised by non-macromolecular compounds, e.g. waxes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M2205/00—Printing methods or features related to printing methods; Location or type of the layers
    • B41M2205/04—Direct thermal recording [DTR]
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M2205/00—Printing methods or features related to printing methods; Location or type of the layers
    • B41M2205/38—Intermediate layers; Layers between substrate and imaging layer
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M2205/00—Printing methods or features related to printing methods; Location or type of the layers
    • B41M2205/40—Cover layers; Layers separated from substrate by imaging layer; Protective layers; Layers applied before imaging

Definitions

  • the present invention relates to a recording material suited for use in direct thermal imaging. More in particular the present invention relates to a recording material based on a heat induced reaction between a substantially light insensitive organic silver salt and a reducing agent.
  • thermography two approaches are known :
  • Thermal dye transfer printing is a recording method wherein a dye-donor element is used that is provided with a dye layer wherefrom dyed portions of incorporated dye is transferred onto a contacting receiver element by the application of heat in a pattern normally controlled by electronic information signals.
  • the optical density of transparencies produced by the thermal transfer procedure is rather low and in most of the commercial systems — in spite of the use of donor elements specially designed for printing transparencies - only reaches 1 to 1.2 (as measured by a Macbeth Quantalog Densitometer Type TD 102) .
  • a considerably higher transmission density is asked for. For instance in the medical diagnostical field a maximal transmission density of at least 2.5 is desired.
  • High optical densities can be obtained using a recording material comprising on a support a heat sensitive layer comprising a substantially light insensitive organic silver salt and a reducing agent.
  • a recording material comprising on a support a heat sensitive layer comprising a substantially light insensitive organic silver salt and a reducing agent.
  • Such material can be image-wise heated using a thermal head causing a reaction between the reducing agent and the substantially light insensitive organic silver salt leading to the formation of metallic silver.
  • To obtain a good thermosensitivity heating is carried by contacting the thermal head with the heat sensitive layer.
  • the density level may be controlled by varying the amount of heat applied to the recording material. This is generally accomplished by controlling the number of heat pulses generated by the thermal head. An image having a grey scale is thus obtained.
  • a recording material comprising on a support (i) a heat sensitive layer comprising a substantially light insensitive organic silver salt, (ii) a protective layer containing a matting agent dispersed in a binder and (iii) a reducing agent being present in the heat sensitive layer and/or another layer on the same side of the support carrying the heat sensitive layer.
  • a method for making an image comprising image-wise heating by means of a thermal head a recording material as defined above said thermal head contacting the protective layer of said recording material.
  • Suitable matting agents for use in connection with the present invention are particles that protrude from the protective layer and they can be organic or inorganic. They should be sufficiently large to avoid the scratches but are on the other hand limited in their size because of pinholes that may occur at places where a matting agent is present due to a reduced thermoconductivity at these places.
  • the matting agent will have an average diameter between 0.7 and 1.5 times the thickness of the protective layer. It is also preferred that the matting agents for use in connection with the present invention are capable of withstanding the temperatures involved in the heating process according to the present invention.
  • the matting agent is preferably spherical in shape and is preferably used in an amount of 0.1 to 50% by weight more preferably in an amount of 0.25 to 30% by weight of the binder.
  • matting agents examples include silicone resin particles, silicates, alumina, polymethylmethacrylate particles, polyacrylate particles etc...
  • Preferred silicate particles having a mildly abrasive character are i.a. clay, China clay, talc (magnesium silicate), mica, silica, calcium silicate, aluminium silicate, and aluminium magnesium silicate. These particles are incorporated in the protective layer in such a way, i.e. by selecting the appropriate size with respect to the thickness of the protective layer and amount as described above, that at least part of them protrudes.
  • talc particles examples of talc particles that can be used advantageously in accordance with the present invention are i.a. :
  • Talc 1 Micro Ace Type P3 having a volume average particle size of 4.5 ⁇ m and 1.29 % by volume thereof having a size higher than 10 ⁇ (commercially available from Nippon Talc, Interorgana Chemiehandel)
  • Talc 2 Mistron Ultramix having a volume average particle size of 3.88 ⁇ m and 1.72 % by volume thereof having a size higher than 10 ⁇ (commercially available from Cyprus Minerals)
  • Talc 3 Micro-talc I.T. Extra having a volume average particle size of 4.33 ⁇ m and 2.43 % by volume thereof having a size higher than 10 ⁇ m (commercially available from Norwegian Talc Minerals)
  • Talc 4 Cyprubond (surface-treated to improve adhesion to the binder) having a volume particle size of 5.28 ⁇ m and 9.22 % by volume thereof having a size higher than 10 ⁇ m (commercially available from Cyprus Minerals) .
  • Talc 7 Micro-talc A.T. Extra having a volume average particle size of 4.32 ⁇ m and 3.76 % by volume thereof having a size higher than 10 ⁇ m (commercially available from Norwegian Talc Minerals)
  • Talc 8 Stellar 600 having a volume average particle size of 5.16 ⁇ m and 6.77 % by volume thereof having a size higher than 10 ⁇ m (commercially available from Norwegian Cyprus Minerals)
  • silicate particles examples include silicate particles, silicate particles, and silicate particles.
  • Silicate 1 Syloid 378, which are silica particles having an average particle size of 4 ⁇ m and 0.06 % by volume thereof having a size higher than 10 ⁇ m (commercially available from Grace)
  • Silicate 2 Iriodin 111, which are mica particles having an average particle size of 4.42 ⁇ and 1.45 % by volume thereof having a size higher than 10 ⁇ m (commercially available from Merck)
  • Silicate 3 Chlorite, which is a magnesium-aluminium silicate having an average particle size of 5.57 ⁇ and 16.58 % by volume thereof having a size higher than 10 ⁇ m (commercially available from Cyprus Minerals)
  • the binder for use in the protective layer in connection with the present invention is preferably polymeric and can be selected from amongst hydrophobic and hydrophilic binders. The latter are preferred in connection with the present invention since it has been found that less dirt forms on the thermal head during printing.
  • the protective layer may also be hardened. Hardening may be carried out by means of UV or electron beam curing or the hardening may be effected using a chemical reaction between a hardening agent and the binder. Suitable hardening agents that can be used to harden a binder having active hydrogens are e.g. polyisocyanates, aldehydes and hydrolysed tetraalkyl orthosilicates.
  • binders examples include e.g. copolymers of styrene and acrylonitrile, copolymers of styrene, acrylonitrile and butadiene, nitrocellulose, copolymers of vinylacetate and vinylchloride which may be partially hydrolysed, polyesters and polycarbonates in particular those according to the following formula:
  • R , R , R , and R each independently represents hydrogen, halogen, a C- j _—Cg alkyl group, a substituted C- ⁇ -Cg alkyl group, a C ⁇ -C cycloalkyl group, a substituted C ⁇ -Cg cycloalkyl group, a Cg-C-L Q aryl group, a substituted Cg-C ⁇ g aryl group, a C7-C 2 aralkyl group, or a substituted C 7 -C 1 2 aralkyl group; and
  • X represents the atoms necessary to complete a 5- to 8-membered alicyclic ring, optionally substituted with a C ⁇ -C alkyl group, a 5- or 6-membered cycloalkyl group or a fused—on 5- or 6—membered cycloalkyl grou .
  • Suitable hydrophilic binders for use in connection with the present invention include polyvinyl alcohol, polyvinyl acetate preferably hydrolysed in amount of 20% by weight or more, polyvinylpyrrolidone, gelatine etc..
  • the hydrophilic binder for use in the protective layer preferably has a weight average molecular weight of at least 20000 g/mol more preferably at least 30000 g/mol.
  • a protective layer that contains a hydrolysed polyvinyl acetate hardened with a tetraalkyl orthosilicate.
  • a lubricant to the protective layer or applying a lubricant on top of the protective layer.
  • the lubricant is preferably used in an amount of 0.1% by weight to 10 % by weight of the binder in the protective layer.
  • Suitable lubricants for use in connection with the present invention are e.g. silicone oils, polysiloxane- polyether copolymers, synthetic oils, saturated hydrocarbons, glycols, fatty acids and salts or esters thereof such as e.g. stearic acid, the zinc salt of stearic acid, methyl ester of stearic acid etc...
  • the lubricant may be hardened together with the binder of the protective layer.
  • a binder having active hydrogens and a polysiloxane having active hydrogens may be hardened by means of e.g. polyisocyanate or a tetraalkyl orthosilicate yielding a hardened protective layer containing a lubricant.
  • the thickness of the protective layer in connection with the present invention is preferably between l ⁇ m and lO ⁇ m, more preferably between 1.5 ⁇ m and 7 ⁇ m.
  • Substantially light-insensitive organic silver salts particularly suited for use according to the present invention are silver salts of aliphatic carboxylic acids known as fatty acids, wherein the aliphatic carbon chain has preferably at least 12 C- atoms, e.g. silver laurate, silver palmitate, silver stearate, silver hydroxystearate, silver oleate and silver behenate, and likewise silver dodecyl sulphonate described in US-P 4,504,575 and silver di-(2-ethylhexyl)-sulfosuccinate described in published European patent application 227 141.
  • Useful modified aliphatic carboxylic acids with thioether group are described e.g.
  • thermoplastic water insoluble resins are used wherein the ingredients can be dispersed homogeneously or form therewith a solid-state solution.
  • thermoplastic water insoluble resins are used wherein the ingredients can be dispersed homogeneously or form therewith a solid-state solution.
  • natural, modified natural or synthetic resins may be used, e.g.
  • cellulose derivatives such as ethylcellulose, cellulose esters, carboxymethylcellulose, starch ethers, polymers derived from CC, ⁇ - ethylenically unsaturated compounds such as polyvinyl chloride, after-chlorinated polyvinyl chloride, copolymers of vinyl chloride and vinylidene chloride, copolymers of vinyl chloride and vinyl acetate, polyvinyl acetate and partially hydrolyzed polyvinyl acetate, polyvinyl alcohol, polyvinyl acetals, e.g. polyvinyl butyral, copolymers of acrylonitrile and acrylamide, polyacrylic acid esters, polymethacrylic acid esters and polyethylene or mixtures thereof.
  • a particularly suitable ecologically interesting (halogen-free) binder is polyvinyl butyral.
  • a polyvinyl butyral containing some vinyl alcohol units is marketed under the trade name BUTVAR B79 of Monsanto USA.
  • the binder to organic silver salt weight ratio is preferably in the range of 0.2 to 6, and the thickness of the image forming layer is preferably in the range of 5 to 16 ⁇ .
  • the above mentioned polymers or mixtures thereof forming the binder may be used in conjunction with waxes or "heat solvents” also called “thermal solvents” or “thermosolvents” improving the penetration of the reducing agent (s) and thereby the reaction speed of the redox-reaction at elevated temperature.
  • heat solvents also called “thermal solvents” or “thermosolvents” improving the penetration of the reducing agent (s) and thereby the reaction speed of the redox-reaction at elevated temperature.
  • heat solvent in this invention is meant a non- hydrolyzable organic material which is in solid state at temperatures below 50 °C but becomes on heating above that temperature a plasticizer for the binder of the layer wherein they are incorporated and possibly act then also as a solvent for at least one of the redox-reactants, e.g. the reducing agent for the organic silver salt.
  • a plasticizer for the binder of the layer wherein they are incorporated and possibly act then also as a solvent for at least one of the redox-reactants, e.g. the reducing agent for the organic silver salt are useful for that purpose are a polyethylene glycol having a mean molecular weight in the range of 1,500 to 20,000 described in US-P 3,347,675.
  • Suitable organic reducing agents for the reduction of substantially light-insensitive organic silver salts are organic compounds containing at least one active hydrogen atom linked to 0, N or C, such as is the case in aromatic di- and tri-hydroxy compounds, e.g. hydroquinone and substituted hydroquinones, catechol, pyrogallol, gallic acid and gallates; aminophenols, METOL (tradename), p-phenylenediamines, alkoxynaphthols, e.g. 4-methoxy-l- naphthol described in US-P 3,094,417, pyrazolidin-3-one type reducing agents, e.g.
  • PHENIDONE (tradename) , pyrazolin-5-ones, indanedione-1,3 derivatives, hydroxytetrone acids, hydroxytetronimides, reductones, and ascorbic acid.
  • Representatives for thermally activated reduction of organic silver salts are described e.g. in US-P 3,074,809, 3,080,254, 3,094,417, 3,887,378 and 4,082, 901.
  • organic reducing agents for use in thermally activated reduction of the substantially light insensitive silver salts are organic compounds containing in their structure two free hydroxy groups (-OH) in ortho-position on a benzene nucleus as is the case in catechol and polyhydroxy spiro-bis-indane compounds corresponding to the following general formula (I) which are preferred for use in the recording material according to the present invention:
  • R represents hydrogen or alkyl, e.g. methyl or ethyl
  • each of R and R (same or different) represents, an alkyl group, preferably methyl group or a cycloalkyl group, e.g. cyclohexyl group
  • each of R and R represents, an alkyl group, preferably methyl group or a cycloalkyl group, e.g. cyclohexyl group
  • each of Z ⁇ x and Z_? represents the atoms necessary to close an aromatic ring or ring system, e.g. benzene ring, substituted with at least two hydroxyl groups in ortho- or para-position and optionally further substituted with at least one hydrocarbon group, e.g an alkyl or aryl group.
  • polyhydroxy-spiro-bis-indane compounds described in US-P 3,440,049 as photographic tanning agent more especially 3,3,3' ,3'-tetramethyl-5, 6,5', 6'-tetrahydroxy-l,1'- spiro-bis-indane (called indane I) and 3,3,3' ,3'-tetrameth 1- 4, 6, 7,4' , 6' , 7'-hexahydroxy-1, 1'-spiro-bis-indane (called indane II) .
  • Indane is also known under the name hydrindene.
  • the reducing agent is added to the heat sensitive layer but all or part of the reducing agent may be added to one or more other layers on the same side of the support as the heat sensitive layer.
  • all or part of the reducing agent may be added to the protective surface layer.
  • the recording material may contain auxiliary reducing agents having poor reducing power in addition to the main reducing agent described above preferably in the heat sensitive layer containing the organic silver salt.
  • auxiliary reducing agents having poor reducing power in addition to the main reducing agent described above preferably in the heat sensitive layer containing the organic silver salt.
  • preferably sterically hindered phenols are used.
  • Sterically hindered phenols as described e.g. in US-P 4,001,026 are examples of such auxiliary reducing agents that can be used in admixture with said organic silver salts without premature reduction reaction and fog-formation at room temperature.
  • reducible silver salt (s) and reducing agents are advantageously used in conjunction with a so-called toning agent known from thermography or photo-thermography.
  • Suitable toning agents are the phthalimides and phthalazinones within the scope of the general formulae described in US-P 4,082,901. Further reference is made to the toning agents described in US-P 3,074,809, 3,446,648 and 3,844,797. Particularly useful toning agents are likewise the heterocyclic toner compounds of the benzoxazine dione or naphthoxazine dione type.
  • an image can be obtained with the above described recording material by image-wise heating the recording material by moving the recording material under a thermal head, said thermal head contacting the protective layer.
  • the recording material may be heated with a temperature of upto 400°C by varying the number of heat pulses given by the thermal head. By varying the number of heat pulses the density of the corresponding image pixel is varied correspondingly.
  • a subbed polyethylene terephthalate support having a thickness of 100 ⁇ m was doctor blade-coated so as to obtain thereon after drying the following heat sensitive layer including : silver behenate 4.42 g/ polyvinyl butyral 4.42 g/m 2 reducing agent S as defined hereinafter 0.84 g/m
  • Reducing agent S is 1,l'-spirobi (lH-indene)-5,5' , 6, 6'-tetrol-
  • a protective layer having the following composition: polycarbonate (see below) 6g/m 2 matting agent (see table 1)
  • Tegoglide 410 (tradename) is a lubricant of the polysiloxane- polyether type.
  • the structure of the polycarbonate used was as follows:
  • PMMA copolymer of styrene, methylmethacrylate, stearyl methacrylate, maleinic acid sodium salt and 2-trimethoxysilylethyl methacrylate.
  • Tospearl 145 (tradename) is a silicone resin particle
  • the recording materials prepared as described above were image- wise heated with a thermal head in a thermal printer so as to obtain a density of 3.2.
  • the obtained minimum density in each case was less than 0.05.
  • the obtained images were then visually inspected for scratches and assigned a number from 0 to 5 to indicate the amount of scratches. A number of 0 indicates that no scratches were found whereas a number of 5 indicates severe scratching of the image.
  • Table 2 Table 2
  • a recording material was prepared similar to the recording materials of example 1 with the exception however that the protective layer was replaced with a layer having the following composition: polyvinyl alcohol 3.5g/m
  • the polyvinyl alcohol used was POLYVIOL W48/20 obtained from Wacker.
  • the thus obtained recording material was printed and evaluated as in example 1. A number of 1 could be assigned to indicate the amount of scratches. Furthermore it was found that no contamination of the thermal head occured.
  • a recording material was prepared as described in example 2 with the exception that on top of the protective layer there was applied a thin layer of Tegoglide 410 (lubricant) in an amount of 18mg/m .
  • Tegoglide 410 lubricant
  • a number of 0 to 1 could be assigned to indicate that practically no scratches were found. Furthermore it was found that no contamination of the thermal head occured.
  • the obtained solution was coated with a Braive knife of 50 ⁇ m to a polyethyleneterephthalate support containing the heat sensitive layer described in example 1.
  • the obtained recording material was dried and heated for 1 hour at 60°C to harden the protective layer.
  • the recording material was then printed and evaluated as described in example 1. No scratches were found on the image. Furthermore it was found that no contamination of the thermal head occured.

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  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)

Abstract

The present invention provides a recording material comprising on a support (i) a heat sensitive layer comprising a substantially light insensitive organic silver salt, (ii) a protective layer containing a matting agent dispersed in a binder and (iii) a reducing agent being present in the heat sensitive layer and/or another layer on the same side of the support carrying the heat sensitive layer. The present invention further provides a method for making images therewith. The obtained images may be used in medical diagnostics.

Description

DESCRIPTION
DIRECT THERMAL IMAGING MATERIAL
Field of the invention.
The present invention relates to a recording material suited for use in direct thermal imaging. More in particular the present invention relates to a recording material based on a heat induced reaction between a substantially light insensitive organic silver salt and a reducing agent.
2. Background of the Invention
In thermography two approaches are known :
1. Direct thermal ormation of a visible image pattern by imagewise heating of a recording material containing matter that by chemical or physical process changes colour or optical density.
2. Thermal dye transfer printing wherein a visible image pattern is formed by transfer of a coloured species from an imagewise heated donor element onto a receptor element.
Thermal dye transfer printing is a recording method wherein a dye-donor element is used that is provided with a dye layer wherefrom dyed portions of incorporated dye is transferred onto a contacting receiver element by the application of heat in a pattern normally controlled by electronic information signals.
The optical density of transparencies produced by the thermal transfer procedure is rather low and in most of the commercial systems — in spite of the use of donor elements specially designed for printing transparencies - only reaches 1 to 1.2 (as measured by a Macbeth Quantalog Densitometer Type TD 102) . However, for many application fields a considerably higher transmission density is asked for. For instance in the medical diagnostical field a maximal transmission density of at least 2.5 is desired.
High optical densities can be obtained using a recording material comprising on a support a heat sensitive layer comprising a substantially light insensitive organic silver salt and a reducing agent. Such material can be image-wise heated using a thermal head causing a reaction between the reducing agent and the substantially light insensitive organic silver salt leading to the formation of metallic silver. To obtain a good thermosensitivity heating is carried by contacting the thermal head with the heat sensitive layer. The density level may be controlled by varying the amount of heat applied to the recording material. This is generally accomplished by controlling the number of heat pulses generated by the thermal head. An image having a grey scale is thus obtained.
Because of its high density the image is in principal suitable for use as a medical diagnostic image. However the following problems have been encounterred. Uneveness of density occurs with the number of images that have been printed and damaging of the heat sensitive layer occurs. These problems can be overcome by making use of a protective layer. Although this brings a substantial improvement so that the image may be suitable for some applications, the images show scratches that are prohibitive for the use of the image in medical diagnostics.
3. Summary of the invention.
It is an object of the present invention to improve the quality of images obtained by direct thermal imaging of a recording material comprising on a support (i) a heat sensitive layer comprising a substantially light insensitive organic silver salt and (ii) a reducing agent being present in the heat sensitive layer or another layer on the same side of the support carrying the heat sensitive layer.
Further objects of the present invention will become clear from the description hereinafter.
According to the present invention there is provided a recording material comprising on a support (i) a heat sensitive layer comprising a substantially light insensitive organic silver salt, (ii) a protective layer containing a matting agent dispersed in a binder and (iii) a reducing agent being present in the heat sensitive layer and/or another layer on the same side of the support carrying the heat sensitive layer.
According to the present invention there is provided a method for making an image comprising image-wise heating by means of a thermal head a recording material as defined above said thermal head contacting the protective layer of said recording material.
4. Detailed description
Thanks to the use of a matting agent in the protective layer the occurrences of scratches can be reduced and in some cases scratches are completely avoided. Suitable matting agents for use in connection with the present invention are particles that protrude from the protective layer and they can be organic or inorganic. They should be sufficiently large to avoid the scratches but are on the other hand limited in their size because of pinholes that may occur at places where a matting agent is present due to a reduced thermoconductivity at these places. Preferably the matting agent will have an average diameter between 0.7 and 1.5 times the thickness of the protective layer. It is also preferred that the matting agents for use in connection with the present invention are capable of withstanding the temperatures involved in the heating process according to the present invention. Generally they should be able to withstand a temperature of upto 400°C without showing substantial deformations. The matting agent is preferably spherical in shape and is preferably used in an amount of 0.1 to 50% by weight more preferably in an amount of 0.25 to 30% by weight of the binder.
Examples of matting agents that can be used are silicone resin particles, silicates, alumina, polymethylmethacrylate particles, polyacrylate particles etc...
Preferred silicate particles having a mildly abrasive character are i.a. clay, China clay, talc (magnesium silicate), mica, silica, calcium silicate, aluminium silicate, and aluminium magnesium silicate. These particles are incorporated in the protective layer in such a way, i.e. by selecting the appropriate size with respect to the thickness of the protective layer and amount as described above, that at least part of them protrudes.
Examples of talc particles that can be used advantageously in accordance with the present invention are i.a. :
Talc 1 : Micro Ace Type P3 having a volume average particle size of 4.5 μm and 1.29 % by volume thereof having a size higher than 10 μ (commercially available from Nippon Talc, Interorgana Chemiehandel)
Talc 2 : Mistron Ultramix having a volume average particle size of 3.88 μm and 1.72 % by volume thereof having a size higher than 10 μ (commercially available from Cyprus Minerals)
Talc 3 : Micro-talc I.T. Extra having a volume average particle size of 4.33 μm and 2.43 % by volume thereof having a size higher than 10 μm (commercially available from Norwegian Talc Minerals) Talc 4 : Cyprubond (surface-treated to improve adhesion to the binder) having a volume particle size of 5.28 μm and 9.22 % by volume thereof having a size higher than 10 μm (commercially available from Cyprus Minerals) .
Talc 5 : MP10-52 having a volume particle size of 3.15 μm and 1.26 % by volume thereof having a size higher than 10 μ (commercially available from Pfizer Minerals)
Talc 6 : MP12-50 having a volume particle size of 2.60 μ and 0.97 % by volume thereof having a size higher than 10 μm (commercially available from Pfizer Minerals)
Talc 7 : Micro-talc A.T. Extra having a volume average particle size of 4.32 μm and 3.76 % by volume thereof having a size higher than 10 μm (commercially available from Norwegian Talc Minerals)
Talc 8 : Stellar 600 having a volume average particle size of 5.16 μm and 6.77 % by volume thereof having a size higher than 10 μm (commercially available from Norwegian Cyprus Minerals)
Examples of other silicate particles that can be used in accordance with the present invention are i.a. :
Silicate 1 : Syloid 378, which are silica particles having an average particle size of 4 μm and 0.06 % by volume thereof having a size higher than 10 μm (commercially available from Grace)
Silicate 2 : Iriodin 111, which are mica particles having an average particle size of 4.42 μ and 1.45 % by volume thereof having a size higher than 10 μm (commercially available from Merck)
Silicate 3 : Chlorite, which is a magnesium-aluminium silicate having an average particle size of 5.57 μ and 16.58 % by volume thereof having a size higher than 10 μm (commercially available from Cyprus Minerals)
The binder for use in the protective layer in connection with the present invention is preferably polymeric and can be selected from amongst hydrophobic and hydrophilic binders. The latter are preferred in connection with the present invention since it has been found that less dirt forms on the thermal head during printing. The protective layer may also be hardened. Hardening may be carried out by means of UV or electron beam curing or the hardening may be effected using a chemical reaction between a hardening agent and the binder. Suitable hardening agents that can be used to harden a binder having active hydrogens are e.g. polyisocyanates, aldehydes and hydrolysed tetraalkyl orthosilicates.
Examples of binders that can be used in connection with the present invention are e.g. copolymers of styrene and acrylonitrile, copolymers of styrene, acrylonitrile and butadiene, nitrocellulose, copolymers of vinylacetate and vinylchloride which may be partially hydrolysed, polyesters and polycarbonates in particular those according to the following formula:
wherein :
R , R , R , and R each independently represents hydrogen, halogen, a C-j_—Cg alkyl group, a substituted C-^-Cg alkyl group, a C^-C cycloalkyl group, a substituted C^-Cg cycloalkyl group, a Cg-C-LQ aryl group, a substituted Cg-C^g aryl group, a C7-C 2 aralkyl group, or a substituted C7-C12 aralkyl group; and
X represents the atoms necessary to complete a 5- to 8-membered alicyclic ring, optionally substituted with a C^-C alkyl group, a 5- or 6-membered cycloalkyl group or a fused—on 5- or 6—membered cycloalkyl grou .
Suitable hydrophilic binders for use in connection with the present invention include polyvinyl alcohol, polyvinyl acetate preferably hydrolysed in amount of 20% by weight or more, polyvinylpyrrolidone, gelatine etc.. The hydrophilic binder for use in the protective layer preferably has a weight average molecular weight of at least 20000 g/mol more preferably at least 30000 g/mol. According to a most preferred embodiment in connection with the present invention there is used a protective layer that contains a hydrolysed polyvinyl acetate hardened with a tetraalkyl orthosilicate.
In accordance with the present invention it is also preferred to add a lubricant to the protective layer or applying a lubricant on top of the protective layer. By using a lubricant transportation problems of the recording material under the thermal head can be avoided as well as image deformations. The lubricant is preferably used in an amount of 0.1% by weight to 10 % by weight of the binder in the protective layer. Suitable lubricants for use in connection with the present invention are e.g. silicone oils, polysiloxane- polyether copolymers, synthetic oils, saturated hydrocarbons, glycols, fatty acids and salts or esters thereof such as e.g. stearic acid, the zinc salt of stearic acid, methyl ester of stearic acid etc...
According to a particular embodiment in connection with the present invention the lubricant may be hardened together with the binder of the protective layer. For example a binder having active hydrogens and a polysiloxane having active hydrogens may be hardened by means of e.g. polyisocyanate or a tetraalkyl orthosilicate yielding a hardened protective layer containing a lubricant.
The thickness of the protective layer in connection with the present invention is preferably between lμm and lOμm, more preferably between 1.5μm and 7μm.
Substantially light-insensitive organic silver salts particularly suited for use according to the present invention are silver salts of aliphatic carboxylic acids known as fatty acids, wherein the aliphatic carbon chain has preferably at least 12 C- atoms, e.g. silver laurate, silver palmitate, silver stearate, silver hydroxystearate, silver oleate and silver behenate, and likewise silver dodecyl sulphonate described in US-P 4,504,575 and silver di-(2-ethylhexyl)-sulfosuccinate described in published European patent application 227 141. Useful modified aliphatic carboxylic acids with thioether group are described e.g. in GB-P 1,111,492 and other organic silver salts are described in GB-P 1,439,478, e.g. silver benzoate and silver phthalazinone, which may be used likewise to produce a thermally developable silver image. Further are mentioned silver imidazolates and the substantially light—insensitive inorganic or organic silver salt complexes described in US-P 4,260,677.
As binding agent for the heat sensitive layer preferably thermoplastic water insoluble resins are used wherein the ingredients can be dispersed homogeneously or form therewith a solid-state solution. For that purpose all kinds of natural, modified natural or synthetic resins may be used, e.g. cellulose derivatives such as ethylcellulose, cellulose esters, carboxymethylcellulose, starch ethers, polymers derived from CC,β- ethylenically unsaturated compounds such as polyvinyl chloride, after-chlorinated polyvinyl chloride, copolymers of vinyl chloride and vinylidene chloride, copolymers of vinyl chloride and vinyl acetate, polyvinyl acetate and partially hydrolyzed polyvinyl acetate, polyvinyl alcohol, polyvinyl acetals, e.g. polyvinyl butyral, copolymers of acrylonitrile and acrylamide, polyacrylic acid esters, polymethacrylic acid esters and polyethylene or mixtures thereof. A particularly suitable ecologically interesting (halogen-free) binder is polyvinyl butyral. A polyvinyl butyral containing some vinyl alcohol units is marketed under the trade name BUTVAR B79 of Monsanto USA.
The binder to organic silver salt weight ratio is preferably in the range of 0.2 to 6, and the thickness of the image forming layer is preferably in the range of 5 to 16 μ .
The above mentioned polymers or mixtures thereof forming the binder may be used in conjunction with waxes or "heat solvents" also called "thermal solvents" or "thermosolvents" improving the penetration of the reducing agent (s) and thereby the reaction speed of the redox-reaction at elevated temperature.
By the term "heat solvent" in this invention is meant a non- hydrolyzable organic material which is in solid state at temperatures below 50 °C but becomes on heating above that temperature a plasticizer for the binder of the layer wherein they are incorporated and possibly act then also as a solvent for at least one of the redox-reactants, e.g. the reducing agent for the organic silver salt. Useful for that purpose are a polyethylene glycol having a mean molecular weight in the range of 1,500 to 20,000 described in US-P 3,347,675. Further are mentioned compounds such as urea, methyl sulfonamide and ethylene carbonate being heat solvents described in US-P 3,667,959, and compounds such as tetrahydro-thiophene-1, 1-dioxide, methyl anisate and 1, 10-deσanediol being described as heat solvents in Research Disclosure, December 1976, (item 15027) pages 26-28. Still other examples of heat solvents have been described in US-P 3,438,776, and 4,740,446, and in published EP-A 0 119 615 and 0 122 512 and DE-A 3 339 810.
Suitable organic reducing agents for the reduction of substantially light-insensitive organic silver salts are organic compounds containing at least one active hydrogen atom linked to 0, N or C, such as is the case in aromatic di- and tri-hydroxy compounds, e.g. hydroquinone and substituted hydroquinones, catechol, pyrogallol, gallic acid and gallates; aminophenols, METOL (tradename), p-phenylenediamines, alkoxynaphthols, e.g. 4-methoxy-l- naphthol described in US-P 3,094,417, pyrazolidin-3-one type reducing agents, e.g. PHENIDONE (tradename) , pyrazolin-5-ones, indanedione-1,3 derivatives, hydroxytetrone acids, hydroxytetronimides, reductones, and ascorbic acid. Representatives for thermally activated reduction of organic silver salts are described e.g. in US-P 3,074,809, 3,080,254, 3,094,417, 3,887,378 and 4,082, 901.
Particularly suited organic reducing agents for use in thermally activated reduction of the substantially light insensitive silver salts are organic compounds containing in their structure two free hydroxy groups (-OH) in ortho-position on a benzene nucleus as is the case in catechol and polyhydroxy spiro-bis-indane compounds corresponding to the following general formula (I) which are preferred for use in the recording material according to the present invention:
wherein :
R represents hydrogen or alkyl, e.g. methyl or ethyl, each of R and R (same or different) represents, an alkyl group, preferably methyl group or a cycloalkyl group, e.g. cyclohexyl group, each of R and R (same or different) represents, an alkyl group, preferably methyl group or a cycloalkyl group, e.g. cyclohexyl group, and each of Zιx and Z_? (same or di■fferent) represents the atoms necessary to close an aromatic ring or ring system, e.g. benzene ring, substituted with at least two hydroxyl groups in ortho- or para-position and optionally further substituted with at least one hydrocarbon group, e.g an alkyl or aryl group.
Particularly useful are the polyhydroxy-spiro-bis-indane compounds described in US-P 3,440,049 as photographic tanning agent, more especially 3,3,3' ,3'-tetramethyl-5, 6,5', 6'-tetrahydroxy-l,1'- spiro-bis-indane (called indane I) and 3,3,3' ,3'-tetrameth 1- 4, 6, 7,4' , 6' , 7'-hexahydroxy-1, 1'-spiro-bis-indane (called indane II) . Indane is also known under the name hydrindene.
Preferably the reducing agent is added to the heat sensitive layer but all or part of the reducing agent may be added to one or more other layers on the same side of the support as the heat sensitive layer. For example, all or part of the reducing agent may be added to the protective surface layer.
The recording material may contain auxiliary reducing agents having poor reducing power in addition to the main reducing agent described above preferably in the heat sensitive layer containing the organic silver salt. For that purpose preferably sterically hindered phenols are used.
Sterically hindered phenols as described e.g. in US-P 4,001,026 are examples of such auxiliary reducing agents that can be used in admixture with said organic silver salts without premature reduction reaction and fog-formation at room temperature.
For obtaining a neutral black image tone with silver formed in the higher optical density parts and neutral grey in the lower densities the reducible silver salt (s) and reducing agents are advantageously used in conjunction with a so-called toning agent known from thermography or photo-thermography.
Suitable toning agents are the phthalimides and phthalazinones within the scope of the general formulae described in US-P 4,082,901. Further reference is made to the toning agents described in US-P 3,074,809, 3,446,648 and 3,844,797. Particularly useful toning agents are likewise the heterocyclic toner compounds of the benzoxazine dione or naphthoxazine dione type.
According to the present invention an image can be obtained with the above described recording material by image-wise heating the recording material by moving the recording material under a thermal head, said thermal head contacting the protective layer. The recording material may be heated with a temperature of upto 400°C by varying the number of heat pulses given by the thermal head. By varying the number of heat pulses the density of the corresponding image pixel is varied correspondingly.
The present invention will now be illustrated by the following examples without however the intention to limit the invention thereto. All parts are by weight unless otherwise specified.
EXAMPLE 1
Preparation of the recording materials:
A subbed polyethylene terephthalate support having a thickness of 100 μm was doctor blade-coated so as to obtain thereon after drying the following heat sensitive layer including : silver behenate 4.42 g/ polyvinyl butyral 4.42 g/m2 reducing agent S as defined hereinafter 0.84 g/m
3,4-dihydro-2,4-dioxo-l,3,2H-benzoxazine 0.34 g/m silicone oil 0.02 g/m2
Reducing agent S is 1,l'-spirobi (lH-indene)-5,5' , 6, 6'-tetrol-
2,2' ,3,3'-tetrahydro—3,3,3',3'-tetramethyl.
To the heat sensitive layer was coated a protective layer having the following composition: polycarbonate (see below) 6g/m2 matting agent (see table 1)
Tegoglide 410* 0.3g/m2
(*) Tegoglide 410 (tradename) is a lubricant of the polysiloxane- polyether type.
The structure of the polycarbonate used was as follows:
wherein x = 55 mol% and y = 45 mol%. Table 1
PMMA= copolymer of styrene, methylmethacrylate, stearyl methacrylate, maleinic acid sodium salt and 2-trimethoxysilylethyl methacrylate. Tospearl 145 (tradename) is a silicone resin particle
The recording materials prepared as described above were image- wise heated with a thermal head in a thermal printer so as to obtain a density of 3.2. The obtained minimum density in each case was less than 0.05. The obtained images were then visually inspected for scratches and assigned a number from 0 to 5 to indicate the amount of scratches. A number of 0 indicates that no scratches were found whereas a number of 5 indicates severe scratching of the image. The obtained results are listed in table 2. Table 2
From the above table it can be seen that the number of scratches on the image can be effectively reduced by adding a matting agent to the protective layer.
EXAMPLE 2
A recording material was prepared similar to the recording materials of example 1 with the exception however that the protective layer was replaced with a layer having the following composition: polyvinyl alcohol 3.5g/m
China Clay (matting agent) 1.5g/m
The polyvinyl alcohol used was POLYVIOL W48/20 obtained from Wacker. The thus obtained recording material was printed and evaluated as in example 1. A number of 1 could be assigned to indicate the amount of scratches. Furthermore it was found that no contamination of the thermal head occured.
EXAMPLE 3
A recording material was prepared as described in example 2 with the exception that on top of the protective layer there was applied a thin layer of Tegoglide 410 (lubricant) in an amount of 18mg/m . A number of 0 to 1 could be assigned to indicate that practically no scratches were found. Furthermore it was found that no contamination of the thermal head occured.
EXAMPLE 4
2 parts of a solution in water containing 7% of polyvinyl alcohol (POLYVIOL W48/20 from Wacker) and 3% of China Clay were mixed with 1 part of an aqueous solution containing 14% of tetramethyl orthosilicate. The mixture was brought to pH=4 using sodium hydroxide.
The obtained solution was coated with a Braive knife of 50μm to a polyethyleneterephthalate support containing the heat sensitive layer described in example 1. The obtained recording material was dried and heated for 1 hour at 60°C to harden the protective layer.
The recording material was then printed and evaluated as described in example 1. No scratches were found on the image. Furthermore it was found that no contamination of the thermal head occured.

Claims

1. A recording material comprising on a support (i) a heat sensitive layer comprising a substantially light insensitive organic silver salt, (ii) a protective layer containing a matting agent dispersed in a binder and (iii) a reducing agent being present in the heat sensitive layer and/or another layer on the same side of the support carrying the heat sensitive layer.
2. A recording material according to claim 1 wherein said binder is a polycarbonate.
3. A recording material according to claim 1 or 2 wherein said protective layer further comprises a lubricant or wherein a lubricant is present on top of said protective layer.
4. A recording material according to claim 1 wherein said binder is hydrophilic.
5. A recording material according to claim 4 wherein said binder is polyvinyl alcohol or a polyvinyl acetate.
6. A recording material according to any of the above claims wherein said protective layer is hardened.
7. A recording material according to any of the above claims wherein the average diameter of said matting agent is between 0.7 and 1.5 times the thickness of the protective layer.
8. A method for making an image comprising image-wise heating a recording material as defined in any of the above claims by means of a thermal head contacting the protective layer of the recording material.
9. Use of an image obtained by the method of claim 8 in medical diagnostics.
EP93924602A 1992-11-16 1993-11-06 Direct thermal imaging material Expired - Lifetime EP0669875B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP93924602A EP0669875B1 (en) 1992-11-16 1993-11-06 Direct thermal imaging material

Applications Claiming Priority (12)

Application Number Priority Date Filing Date Title
EP92203495 1992-11-16
EP92203495 1992-11-16
EP92204009 1992-12-18
EP92204009 1992-12-18
EP93200652 1993-03-08
EP93200652 1993-03-08
EP93200653 1993-03-08
EP93200653 1993-03-08
EP93202599A EP0641669B1 (en) 1993-09-07 1993-09-07 Ink jet recording method operating with a chemically reactive ink
EP93202599 1993-09-08
EP93924602A EP0669875B1 (en) 1992-11-16 1993-11-06 Direct thermal imaging material
PCT/EP1993/003120 WO1994011198A1 (en) 1992-11-16 1993-11-06 Direct thermal imaging material

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EP0669875A1 true EP0669875A1 (en) 1995-09-06
EP0669875B1 EP0669875B1 (en) 1996-04-24

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0846565A1 (en) 1996-11-28 1998-06-10 Agfa-Gevaert N.V. Thermal printer with sheet pressure means

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7071143B2 (en) 2004-01-28 2006-07-04 Eastman Kodak Company Direct thermographic materials with improved protective layers

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9411198A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0846565A1 (en) 1996-11-28 1998-06-10 Agfa-Gevaert N.V. Thermal printer with sheet pressure means

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