Field of the invention
[0001] The present invention relates to a substantially light-insensitive thermographic
recording material suitable for thermal development. In particular, it concerns improvements
in stabilization thereof.
Background of the invention
[0002] Thermal imaging or thermography is a recording process wherein images are generated
by the use of imagewise modulated thermal energy. A survey of "direct thermal" imaging
methods is given e.g. in the book "Imaging Systems" by Kurt I. Jacobson-Ralph E. Jacobson,
The Focal Press - London and New York (1976), Chapter VII under the heading "7.1 Thermography".
Direct thermal thermography is concerned with materials which are substantially not
photosensitive, but are sensitive to heat or thermosensitive. Imagewise applied heat
is sufficient to bring about a visible change in a thermosensitive imaging material.
[0003] WO 94/16361 discloses a multilayer heat-sensitive material for direct thermal recording
for which no intermediate drying of organic noble metal salts is necessary and which
is coatable from aqueous dispersions. This material comprises: a colour-forming amount
of finely divided, solid colourless noble metal or iron salt of an organic acid distributed
in a carrier composition; a color-developing amount of a cyclic or aromatic organic
reducing agent, which at thermal copy and printing temperatures is capable of a colour-forming
reaction with the noble metal or iron salt; and an image toning agent; characterized
in that (a) the carrier composition comprises a substantially water-soluble polymeric
carrier and a dispersing agent for the noble metal or iron salt and (b) the material
comprises a protective overcoating layer for the colour-forming layer. This patent
application also discloses that suitable antifoggants for use in the invention are
well-known photographic antifoggants such as 2-mercaptobenzo-triazole, chromate, oxalate,
carbonate, benzotriazole (BZT), 5-methylbenzotriazole, 5,6-dimethylbenzotriazole,
5-bromobenzotriazole, 5-chlorobenzo-triazole, 5-nitrobenzotriazole, 4-nitro-6-chlorobenzotriazole,
5-nitro-6-chlorobenzotriazole, 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene, benzimidazole,
2-methylbenzimidazole, 5-nitrobenzimidazole, 1-phenyl-5-mercaptotetrazole (PMT), 2-mercaptobenzimidazole,
2-mercaptobenzothiazole, 2-mercaptobenzoxazole, 2-mercaptothiazoline, 2-mercapto-4-methyl-6,6'-dimethylpyrimidine,
1-ethyl-2-mercapto-5-amino-1,3,4-triazole, 1-ethyl-5-mercapto-1,2,3,4-tetrazole, 2,5-dimercapto-1,3,4-thiodiazole,
2-mercapto-5-amino-1,3,4-thiodiazole, dimethyldithiocarbamate, and diethyldithiocarbamate.
[0004] EP-A 809 143 discloses a substantially non-photosensitive recording material comprising
a thermosensitive element comprising a substantially light-insensitive organic silver
salt, an organic reducing agent therefor in thermal working relationship therewith
and a binder, on a support, characterized in that the thermosensitive element further
comprises in reactive association with the substantially light-insensitive organic
silver salt and the organic reducing agent a substituted or unsubstituted compound
with an unsaturated 5-membered heterocyclic ring consisting of nitrogen and carbon
atoms with at least one of the nitrogen atoms having a hydrogen atom and none of the
carbon atoms being part of a thione-group, the ring not being annulated with an aromatic
ring system and the compound being exclusive of 1,2,4-triazole and substituted 1,2,4-triazole
compounds.
[0005] EP-A 809 144 discloses a substantially non-photosensitive recording material comprising
a thermosensitive element comprising a substantially light-insensitive organic silver
salt, an organic reducing agent therefor in thermal working relationship therewith
and a binder, on a support, characterized in that the thermosensitive element further
comprises in reactive association with the substantially light-insensitive organic
silver salt and the organic reducing agent a substituted or unsubstituted 1,2,4-triazole
compound with at least one of the nitrogen atoms having a hydrogen atom and none of
the carbon atoms being part of a thione-group, the compound not being annulated with
an aromatic ring system.
[0006] EP-A 809 142 discloses a recording material comprising a support, a thermosensitive
element and a protective layer therefor, the thermosensitive element comprising a
substantially light-insensitive organic silver salt, an organic reducing agent therefor
in thermal working relationship therewith and a binder, wherein the thermosensitive
element further comprises in reactive association with the substantially light-insensitive
organic silver salt and the organic reducing agent a substituted, exclusive of groups
having an exclusively electron withdrawing character, or unsubstituted compound with
an unsaturated 5-membered heterocyclic ring annulated with an aromatic ring system,
the ring consisting of nitrogen and carbon atoms with at least one of the nitrogen
atoms having a hydrogen atom and none of the carbon atoms being directly linked to
a sulfur atom or being part of a carbonyl-group.
[0007] Prior art stabilizers have been found by the inventors to be unsuitable for stabilizing
thermographic materials for graphics applications during storage prior to use.
Objects of the invention.
[0008] It is therefore an object of the invention to provide a means of stabilizing the
image of thermographic recording materials during storage.
[0009] It is a further object of the invention to provide a process utilizing a substantially
non-photosensitive recording material with improved light stabilization to obtain
a direct thermal image.
[0010] Further objects and advantages of the invention will become apparent from the description
hereinafter.
Summary of the invention
[0011] EP-A 809 142, EP-A 809 143 and EP-A 809 144 address the problem of background colour
resulting from exposure to light, which is a particular problem in thermographic materials
used for producing continuous tone transparencies for medical and other applications
having numerical gradation values less than or equal to 2.3. The present invention
addresses the problem of stabilization of the background density during storage prior
to use of the intrinsically more thermosensitive thermographic materials based on
substantially light-insensitive organic silver salts and reducing agents used for
producing steep gradation, so-called graphics images, with numerical gradation values
greater than 2.3 as transparencies or on a white support, for which the prior art
stabilizers are unsuitable.
[0012] The above mentioned objects are realised by a substantially light-insensitive monosheet
recording material comprising a support and a thermosensitive element containing a
substantially light-insensitive organic silver salt, an organic reducing agent therefor
in thermal working relationship therewith and a binder, characterized in that the
thermosensitive element further contains an unsaturated carbocyclic or heterocyclic
stabilizer compound substituted with a -SA group where A is hydrogen, a counterion
to compensate the negative charge of the thiolate group or a group forming a symmetrical
or an asymmetrical disulfide and the recording material is capable of producing prints
with a numerical gradation value defined as the quotient of the fraction (2.5 - 0.1)/(E
2.5 - E
0.1) greater than 2.3 , where E
2.5 is the energy in Joule applied in a dot area of 87 µm x 87 µm of the imaging layer
that produces an optical density value of 2.5, and E
0.1 is the energy in Joule applied in a dot area of the imaging layer material that produces
an optical density value of 0.1.
[0013] A thermal image recording process is also provided comprising the steps of: (i) providing
a substantially light-insensitive recording material, as described above; (ii) bringing
an outermost layer of the recording material into proximity with a heat source; (iii)
applying heat from a heat source image-wise to the recording material while maintaining
proximity to the heat source to produce an image; and (iv) separating the recording
material from the heat source.
[0014] Preferred embodiments of the invention are disclosed in the dependent claims.
Detailed description of the invention
[0015] According to preferred embodiment a thermal image forming process, according to the
present invention, is realized, wherein the heat source is a thermal head.
Substantially
[0016] By substantially light-insensitive is meant not intentionally light sensitive.
Stabilizer compounds
[0017] The stabilizer compound for use in the present invention may be further substituted,
which substitution also includes the atoms necessary to form an annulated unsaturated
carbocyclic or heterocyclic ring system. Preferred substituents include acylamido,
aryl-SO
2NH-, alkyl-SO
2NH-, aryl-NHSO
2-, alkyl-NHSO
2-, arylamino, alkyl, aryl, nitro and cyano groups and halogen atoms. Preferred stablizer
compounds used in the present invention have an unsaturated 5- or 6-membered ring.
According to a preferred embodiment of the stabilizer compounds used in the present
invention the stabilizer compound is represented by formula (I) :

where Q are the necessary atoms to form a 5- or 6-membered aromatic heterocyclic
ring, which may also be substituted, A is selected from hydrogen, a counterion to
compensate the negative charge of the thiolate group or a group forming a symmetrical
or an asymmetrical disulfide.
[0018] Particularly preferred stabilizer compounds used in the present invention are represented
by the formulae:

Thermosensitive element
[0020] The thermosensitive element, according to the present invention, comprises a substantially
light-insensitive organic silver salt and an organic reducing agent therefor in thermal
working relationship therewith in reactive association with a compound with an unsaturated
5-membered heterocyclic ring. The element may comprise a layer system in which the
ingredients may be dispersed in different layers, with the proviso that all three
ingredients are in reactive association with one another i.e. during the thermal development
process the reducing agent and the stabilizer compound must be present in such a way
that they are able to diffuse to the substantially light-insensitive organic silver
salt particles so that reduction of the organic silver salt to silver giving the desired
image-tone can take place. Furthermore the stabilizer compound must be present in
such a way that the thermosensitive element can be stabilized against the influence
of light.
Organic silver salts
[0021] Preferred organic silver salts 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, with silver behenate
being particularly preferred. Such silver salts are also called "silver soaps". In
addition silver dodecyl sulphonate described in US-P 4,504,575; and silver di-(2-ethylhexyl)-sulfosuccinate
described in EP-A 227 141, modified aliphatic carboxylic acids with thioether group
as described e.g. in GB-P 1,111,492 and other organic silver salts as described in
GB-P 1,439,478, e.g. silver benzoate and silver phthalazinone, 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. Combinations of different organic silver salts can also
be used in the recording materials of the present invention.
Reducing agents
[0022] Suitable organic reducing agents for the reduction of the substantially light-insensitive
organic silver salts are organic compounds containing at least one active hydrogen
atom linked to O, N or C, such as is the case with, aromatic di- and tri-hydroxy compounds;
aminophenols; METOL™; p-phenylenediamines; alkoxynaphthols, e.g. 4-methoxy-1-naphthol
described in US-P 3,094,41; pyrazolidin-3-one type reducing agents, e.g. PHENIDONE™;
pyrazolin-5-ones; indan-1,3-dione derivatives; hydroxytetrone acids; hydroxytetronimides;
hydroxylamine derivatives such as for example described in US-P 4,082,901; hydrazine
derivatives; and reductones e.g. ascorbic acid; see also US-P 3,074,809, 3,080,254,
3,094,417 and 3,887,378. Preferred catechol-type reducing agents are benzene compounds
in which the benzene nucleus is substituted by no more than two hydroxy groups which
are present in 3,4-position on the nucleus and have in the 1-position of the nucleus
a substituent linked to the nucleus by means of a carbonyl group disclosed in EP-A
692 733.
[0023] The silver image density depends on the coverage of the above defined reducing agent(s)
and organic silver salt(s) and has to be preferably such that, on heating above 100
°C, an optical density of at least 2.5 can be obtained. Preferably at least 0.10 moles
of reducing agent per mole of organic silver salt is used.
Auxiliary reducing agents
[0024] The above mentioned reducing agents, regarded as primary or main reducing agents,
may be used in conjunction with so-called auxiliary reducing agents. Such auxiliary
reducing agents are e.g. sterically hindered phenols, such as described in US-P 4,001,026;
bisphenols, e.g. of the type described in US-P 3,547,648; or sulfonamidophenols as
described in Research Disclosure 17842 published in February 1979, US-P 4,360,581,
US-P 4,782,004 and in EP-A 423 891. The auxiliary reducing agents may be present in
the imaging layer or in a polymeric binder layer in thermal working relationship thereto.
[0025] Other auxiliary reducing agents that may be used in conjunction with the above mentioned
primary reducing agents are hydrazides such as disclosed in EP-A 762 196, sulfonyl
hydrazide reducing agents such as disclosed in US-P 5,464,738; trityl hydrazides and
formyl-phenyl-hydrazides such as disclosed in US-P 5,496,695; trityl hydrazides and
formyl-phenyl-hydrazides with diverse auxiliary reducing agents such as disclosed
in US-P 5,545,505, US-P 5.545.507 and US-P 5,558,983; acrylonitrile compounds as disclosed
in US-P 5,545,515 and US-P 5,635,339; and organic reducing metal salts, e.g. stannous
stearate described in US-P 3,460,946 and 3,547,648.
Polycarboxylic acids and anhydrides thereof
[0026] According to the substantially light-insensitive recording material of the present
invention the thermosensitive element may comprise in addition at least one polycarboxylic
acid and/or anhydride thereof in a molar percentage of at least 15 with respect to
all the organic silver salt(s) present and in thermal working relationship therewith.
The polycarboxylic acid may be aliphatic (saturated as well as unsaturated aliphatic
and also cycloaliphatic) or an aromatic polycarboxylic acid, may be substituted and
may be used in anhydride form or partially esterified on the condition that at least
two free carboxylic acids remain or are available in the heat recording step.
Binders
[0027] The film-forming binder of the thermosensitive element containing the substantially
light-insensitive organic silver salt may be all kinds of natural, modified natural
or synthetic resins or mixtures of such resins, wherein the organic silver salts can
be dispersed homogeneously: e.g. cellulose derivatives such as ethylcellulose, cellulose
esters, e.g. cellulose nitrate, carboxymethylcellulose, starch ethers, galactomannan,
polyesters, polyurethanes, polycarbonates, polymers derived from α,β-ethylenically
unsaturated compounds such as after-chlorinated polyvinyl chloride, partially hydrolyzed
polyvinyl acetate, polyvinyl alcohol, polyvinyl acetals, preferably polyvinyl butyral,
and homopolymers and copolymers produced using monomers selected from the group consisting
of: vinyl chloride, vinylidene chloride, acrylonitrile, acrylamides, methacrylamides;
methacrylates, acrylates, methacrylic acid, acrylic acid, vinyl esters, styrenes,
dienes and alkenes; or mixtures thereof.
[0028] The layer containing the organic silver salt is commonly coated onto a support in
sheet- or web-form from an organic solvent containing the binder dissolved therein,
but may be applied from an aqueous medium as a latex, i.e. as an aqueous polymer dispersion.
For use as a latex the dispersible polymer has preferably some hydrophilic functionality.
Binder to organic silver salt ratio
[0029] The ratio of the total weight of any binders in the thermosensitive element to the
total weight of organic silver salts in the thermosensitive element is preferably
less than 2.0 and the thickness of the recording layer is preferably in the range
of 5 to 50 µm.
Thermal solvent
[0030] The above mentioned binders or mixtures thereof may be used in conjunction with waxes
or "heat solvents" also called "thermal solvents" or "thermosolvents" improving the
reaction speed of the redox-reaction at elevated temperature.
[0031] By the term "heat solvent" in this invention is meant a non-hydrolyzable organic
material which is in solid state in the recording layer at temperatures below 50°C
but becomes a plasticizer for the recording layer in the heated region and/or liquid
solvent for at least one of the redox-reactants, e.g. the reducing agent for the organic
heavy metal salt, at a temperature above 60°C.
Toning agent
[0032] In order to obtain a neutral black image tone in the higher densities and neutral
grey in the lower densities the recording layer contains preferably in admixture with
the organic silver salts and reducing agents a so-called toning agent known from thermography
or photothermography. Suitable toning agents are the phthalimides and phthalazinones
within the scope of the general formulae described in US-P 4,082,901. Other particularly
useful toning agents are the heterocyclic toner compounds of the benzoxazine dione
or naphthoxazine dione type are described in GB-P 1,439,478, US-P 3,951,660 and US-P
5,599,647.
Other additives
[0033] The recording layer may contain in addition to the ingredients mentioned above other
additives such as free fatty acids, surface-active agents, antistatic agents, e.g.
non-ionic antistatic agents including a fluorocarbon group as e.g. in F
3C(CF
2)
6CONH(CH
2CH
2O)-H, silicone oil, ultraviolet light absorbing compounds, white light reflecting
and/or ultraviolet radiation reflecting pigments and/or optical brightening agents.
Support
[0034] The support for the thermal imaging material according to the present invention may
be transparent, translucent or opaque, e.g. having a white light reflecting aspect
and is preferably a thin flexible carrier made e.g. from paper, polyethylene coated
paper or transparent resin film, e.g. made of a cellulose ester, e.g. cellulose triacetate,
polypropylene, polycarbonate or polyester, e.g. polyethylene terephthalate.
[0035] The support may be in sheet, ribbon or web form and subbed if need be to improve
the adherence to the thereon coated thermosensitive recording layer. The support may
be made of an opacified resin composition as described in EP's 194 106 and 234 563
and US-P's 3,944,699, 4,187,113, 4,780,402 and 5,059,579. Should a transparent base
be used, the base may be colourless or coloured, e.g. having a blue colour. One or
more backing layers may be provided to control physical properties such as curl.
Outermost layer
[0036] The outermost layer of the substantially light-insensitive recording material may
in different embodiments of the present invention be the outermost layer of the thermosensitive
element, a protective layer applied to the thermosensitive element or a layer on the
opposite side of the support to the thermosensitive element.
Protective layer
[0037] According to a preferred embodiment of the substantially light-insensitive recording
material, according to the present invention, the thermosensitive element is coated
with a protective layer to avoid local deformation of the thermosensitive element
and to improve resistance against abrasion.
[0038] The protective layer preferably comprises a binder, which may be hydrophobic (solvent
soluble) of hydrophilic (water soluble). Among the hydrophobic binders polycarbonates
as described in EP-A 614 769 are particularly preferred. However, hydrophilic binders
are preferred for the protective layer, as coating can be performed from an aqueous
composition and mixing of the hydrophilic protective layer with the immediate underlayer
can be avoided by using a hydrophobic binder in the immediate underlayer.
[0039] A protective layer according to the present invention may further comprise a thermomeltable
particle optionally with a lubricant present on top of the protective layer as described
in WO 94/11199. The lubricant, which may be a surface active agent, a solid lubricant
or a liquid lubricant, may be applied with or without a polymeric binder. Other additives
can also be incorporated in the protective layer e.g. colloidal particles such as
colloidal silica.
Hydrophilic binder for outermost layer
[0040] According to an embodiment of the present invention the outermost layer of the substantially
light-insensitive recording material may comprise a hydrophilic binder Suitable hydrophilic
binders for the outermost layer are, for example, gelatin, polyvinylalcohol, cellulose
derivatives or other polysaccharides, hydroxyethylcellulose, hydroxypropylcellulose
etc., with hardenable binders being preferred and polyvinylalcohol being particularly
preferred.
Crosslinking agents for outermost layer
[0041] The outermost layer according to the present invention may be crosslinked. Crosslinking
can be achieved by using crosslinking agents such as described in WO 95/12495 for
protective layers, e.g. tetra-alkoxysilanes, polyisocyanates, zirconates, titanates,
melamine resins etc., with tetraalkoxysilanes such as tetramethylorthosilicate and
tetraethylorthosilicate being preferred.
Matting agents for outermost layer
[0042] The outermost layer of the substantially light-insensitive recording material according
to the present invention may comprise a matting agent. Suitable matting agents are
described in WO 94/11198 and include e.g. talc particles and optionally protrude from
the outermost layer.
Lubricants for outermost layer
[0043] Solid or liquid lubricants or combinations thereof such as described above for use
in protective layers are also suitable for incorporation in the outermost layer to
improve the slip characteristics of the substantially light-insensitive recording
materials according to the present invention.
Antistatic layer
[0044] In a preferred embodiment the substantially light-insensitive recording material
of the present invention an antistatic layer is the outermost layer on the other side
of the support to the thermosensitive element.
Coating
[0045] The coating of any layer of the substantially light-insensitive recording material
of the present invention may proceed by any coating technique e.g. such as described
in Modern Coating and Drying Technology, edited by Edward D. Cohen and Edgar B. Gutoff,
(1992) VCH Publishers Inc., 220 East 23rd Street, Suite 909 New York, NY 10010, U.S.A.
Processing configurations
[0046] Thermographic imaging is carried out by the image-wise application of heat either
in analogue fashion by direct exposure through an image of by reflection from an image,
or in digital fashion pixel by pixel either by using an infra-red heat source, for
example with a Nd-YAG laser or other infra-red laser, or by direct thermal imaging
with a thermal head.
[0047] In thermal printing image signals are converted into electric pulses and then through
a driver circuit selectively transferred to a thermal printhead. The thermal printhead
consists of microscopic heat resistor elements, which convert the electrical energy
via the Joule effect into heat, which is transferred to the surface of the thermographic
material, wherein the chemical reaction resulting in the development of a black and
white image takes place. Such thermal printing heads may be used in contact or close
proximity with the recording layer. The operating temperature of common thermal printheads
is in the range of 300 to 400°C and the heating time per picture element (pixel) may
be less than 1.0 ms, the pressure contact of the thermal printhead with the recording
material being e.g. 200-500g/cm
2 to ensure a good transfer of heat.
[0048] In order to avoid direct contact of the thermal printing heads with a recording layer
not provided with an outermost protective layer, the image-wise heating of the recording
layer with the thermal printing heads may proceed through a contacting but removable
resin sheet or web wherefrom during the heating no transfer of recording material
can take place.
[0049] The image signals for modulating the laser beam or current in the micro-resistors
of a thermal printhead are obtained directly or from an intermediary storage means.
Activation of the heating elements can be power-modulated or pulse-length modulated
at constant power. EP-A 654 355 describes a method for making an image by image-wise
heating by means of a thermal head having energizable heating elements, wherein the
activation of the heating elements is executed duty cycled pulse-wise. When used in
thermographic recording operating with thermal printheads the thermographic materials
are not suitable for reproducing images with fairly large number of grey levels as
is required for continuous tone reproduction. EP-A 622 217 discloses a method for
making an image using a direct thermal imaging element producing improvements in continuous
tone reproduction. Image-wise heating of the thermographic material can also be carried
out using an electrically resistive ribbon incorporated into the material. Image-
or pattern-wise heating of the thermographic material may also proceed by means of
pixel-wise modulated ultra-sound, using e.g. an ultrasonic pixel printer as described
e.g. in US-P 4,908,631.
Industrial application
[0050] Direct thermal imaging can be used for both the production of transparencies and
reflection type prints. Application of the present invention is envisaged in the fields
of graphics images requiring high contrast images with a very steep print density
applied dot energy dependence. In the hard copy field substantially light-insensitive
recording materials on a white opaque base are used as well as transparencies used
in inspection techniques operating with a light box.
[0051] While the present invention will hereinafter be described in connection with a preferred
embodiment thereof, it will be understood that it is not intended to limit the invention
to that embodiment. On the contrary, it is intended to cover all alternatives, modifications,
and equivalents as may be included within the spirit and scope of the invention as
defined by the appending claims. The invention is illustrated hereinafter by way of
invention examples and comparative examples. The percentages and ratios given in these
examples are by weight unless otherwise indicated. The ingredients used in the INVENTION
and COMPARATIVE EXAMPLES which are not elucidated in the EXAMPLES are:
- Surfactant Nr. 1 =
- MERSOLAT™ H80, a sodium hexadecyl-sulfonate from Bayer;
- Surfactant Nr. 2 =
- ULTRAVON™ W, a sodium arylsulfonate from Ciba-Geigy;
- AgBeh:
- silver behenate, the organic silver salt used;
- B79
- : BUTVAR™ B79, a polyvinyl butyral from Monsanto;
- R01:
- ethyl 3,4-dihydroxybenzoate, the organic reducing agent;
- T01:
- benzo[e][1,3]oxazine-2,4-dione, the toning agents;
- Oil:
- Baysilone™ A from Bayer AG, used as a levelling agent;
COMPARATIVE EXAMPLE 1 & INVENTION EXAMPLES 1 to 5
thermosensitive element
[0052] A 100µm thick support coated with the following subbing-layer composition:
# terpolymer latex of vinylidene chloride/methyl acrylate/itaconic acid (88/10/2): |
162mg/m2 |
# colloidal silica (KIESELSOL™ 100F from BAYER): |
38mg/m2 |
# alkyl sulfonate surfactant (Surfactant Nr. 1): |
0.6mg/m2 |
# aryl sulfonate surfactant (Surfactant Nr. 2): |
4mg/m2 |
was doctor blade-coated with a coating composition containing butanone as a solvent
and the following ingredients so as to obtain thereon. After drying for 1 hour at
room temperature and then 1 hour at 50°C, layers with the compositions given in table
1 for COMPARATIVE EXAMPLE 1 and INVENTION EXAMPLES 1 to 5 were obtained.
Table 1
Comparative Example nr |
AgBeh [g/m2] |
B79 [g/m2] |
R01 [g/m2] |
T01 [g/m2] |
Oil [g/m2] |
stabilizer compound |
|
|
|
|
|
|
type |
[g/m2] |
1 |
5.2 |
5.2 |
0.97 |
0.38 |
0.017 |
- |
- |
Invention Example nr |
|
|
|
|
|
|
|
1 |
5.2 |
5.2 |
0.97 |
0.38 |
0.017 |
S-II |
0.20 |
2 |
5.2 |
5.2 |
0.97 |
0.38 |
0.017 |
S-II |
0.81 |
3 |
5.2 |
5.2 |
0.97 |
0.38 |
0.017 |
S-VIII |
0.12 |
4 |
5.2 |
5.2 |
0.97 |
0.38 |
0.017 |
S-VII |
0.21 |
5 |
5.2 |
5.2 |
0.97 |
0.38 |
0.017 |
S-VII |
0.83 |
Thermographic printing
[0053] During printing of the recording materials of COMPARATIVE EXAMPLE 1 and INVENTION
EXAMPLES 1 to 5 the print head was separated from the imaging layer by a thin intermediate
material contacted with a slipping layer of a separable 5µm thick polyethylene terephthalate
ribbon coated successively with a subbing layer, heat-resistant layer and the slipping
layer (anti-friction layer) giving a ribbon with a total thickness of 6µm.
[0054] The printer was equipped with a thin film thermal head with a resolution of 300 dpi
and was operated with a line time of 32ms (the line time being the time needed for
printing one line). During this line time the print head received constant power.
The average printing power, being the total amount of electrical input energy during
one line time divided by the line time and by the surface area of the heat-generating
resistors was 1.86 mJ/dot being sufficient to obtain maximum optical density in each
of the thermographic materials of COMPARATIVE EXAMPLE 1 and INVENTION EXAMPLES 1 to
5.
Image evaluation
[0055] The maximum densities, D
max, and minimum densities D
min, of the prints were measured through a blue filter with a MacBeth™ TR904 densitometer
in the grey scale step corresponding to data levels of 255 and 0 respectively and
are given in table 2.
Shelf-life test
[0056] The shelf-life of prints made with the thermographic materials of COMPARATIVE EXAMPLE
1 and INVENTION EXAMPLES 1 to 5 was evaluated on the basis of the observed changes
in minimum density, ΔD
min, and maximum density, ΔD
max, printing the thermographic recording materials before and after heating the materials
at 57°C in a relative humidity (RH) of 34% for 3 days in the dark. The results are
given in table 2.
Table 2
Comparative Example number |
stabilizer compound |
FRESH |
SHELF-LIFE TEST 3d at 57°C/34%RH |
|
type |
[g/m2] |
Dmin (blue) |
Dmax/Dmin (ortho) |
numerical gradation value |
ΔDmin (blue) |
ΔDmax/ΔDmin (ortho) |
1 |
- |
- |
0.07 |
4.3/0.07 |
4.7 |
+0.03 |
-0.49/+0.01 |
Invention Example nr |
|
|
|
|
|
|
|
1 |
S-II |
0.20 |
0.08 |
3.8/0.07 |
4.9 |
0.00 |
+0.1/0.00 |
2 |
S-II |
0.81 |
0.08 |
3.1/0.07 |
3.8 |
0.00 |
+0.5/0.00 |
3 |
S-VIII |
0.12 |
0.08 |
3.7/0.08 |
4.5 |
0.00 |
0.0/-0.01 |
4 |
S-VII |
0.21 |
0.07 |
3.4/0.06 |
4.3 |
-0.01 |
+0.5/0.00 |
5 |
S-VII |
0.83 |
0.05 |
2.8/0.05 |
2.5 |
+0.02 |
+0.2/-0.01 |
A comparison of the results obtained with the substantially light-insensitive recording
materials of INVENTION EXAMPLES 1 to 5 with those obtained with the substantially
light-insensitive recording materials of COMPARATIVE EXAMPLE 1 show that stabilizer
compounds S-II, S-VII and S-VIII exhibit a stabilizing effect on D
min measured through a blue filter, as seen by a reduction in ΔD
min (blue), and for the most part also measured through an ortho filter as seen by a
reduction in ΔD
min (ortho), while for the most part having a less reducing affect on D
max measured through an ortho filter, as seen by more positive ΔD
max (ortho) values.
[0057] Having described in detail preferred embodiments of the current invention, it will
now be apparent to those skilled in the art that numerous modifications can be made
therein without departing from the scope of the invention as defined in the following
claims.