Field of the invention
[0001] The present invention concerns the use of substantially light-insensitive monosheet
direct thermal imaging materials for producing labels.
Background of the invention
[0002] Thermal imaging or thermography is a recording process wherein images are generated
by the use of thermal energy. In direct thermal printing a visible image pattern is
produced by image-wise heating of a recording material e.g. image signals can be converted
into electric pulses and then via a driver circuit selectively transferred to a thermal
printhead, which consists of microscopic heat resistor elements, thereby converting
the electrical energy into heat via the Joule effect. This heat brings about image
formation in the thermographic material.
[0003] Label-printing by means of thermography is known with tapes on the basis of monosheet
materials such as colourless or light coloured dye precursor leuco-dye systems, as
disclosed in US-P 4,370,370, EP-A 479 578 and EP-A 754 564, diazo systems, as disclosed
in JP 60-01077A, or two-sheet thermal dye transfer systems, such as disclosed in EP-A
656 264 and US-P 4,943,555.
[0004] WO 87/03541A discloses a recording material which comprises (a) at least one di-
or triarylmethane dye precursor compound possessing within its di- or triarylmethane
structure an aryl group substituted in the ortho position to the meso carbon atom
with an S-containing moiety ring-closed on the meso carbon atom selected from a thiolactone,
dithiolactone and thioether moiety and (b) a Lewis acid material capable of opening
said S-containing moiety whereby said compound is rendered colourless, which Lewis
acid material can be an organic silver salt. US 5,750,464 and US 5,411,929A disclose
refinements of the concept of WO 87/03541A in which the organic silver salt opens
the S-containing moiety rendering said compound containing the S-containing moiety
colourless.
[0005] US-P 3,708,378 provides a single integral imaging sheet that in a single rapid operation
may be converted to a label carrying the desired retro-reflective informative symbols.
It discloses a light-stable heat-sensitive imaging sheet on which retro-reflective
images may be rapidly defined comprising (1) a support layer, (2) a uniform continuous
monolayer of retro-reflective elements disposed on one side of the support layer,
and (3) an imaging layer disposed over the retro-reflective elements comprising, in
uniform distribution throughout the layer, a light-stable heat-sensitive material
that is rapidly chemically modified as to its light-transmitting properties by exposure
to heat, the imaging layer being selected from the group consisting of (1) normally
transparent light-stable layers that are adapted to be converted to transparent when
exposed to heat and (2) normally opaque light-stable layers that are adapted to be
converted to transparent when exposed to heat, whereby light beamed against the sheet
will be retro-reflected only by retro-reflective elements exposed through the transparent
areas. Examples 1 and 2 both disclose a silver behenate-based imaging layer using
methyl gallate as a reducing agent therefor.
[0006] US 3,708,378 contains no teaching about the use of organic silver salt-based materials
for conventional labelling applications. The patent literature over thermographic
materials for labelling applications in the intervening twenty-eight years has exclusively
concerned other imaging systems monosheet materials such as the above-mentioned leuco-dye
systems.
[0007] Labels produced with monosheet thermographic materials based on leuco-dyes have a
well-known propensity to fade when exposed to light, the thermographic materials disclosed
in US 5,750,464, US 5,411,929A and WO 87/03541A concern colour removal rather than
colour formation, and thermal dye transfer systems are expensive to assemble and produce
waste due to the disposal of the donor lint resulting in ecological objections.
Objects of the invention.
[0008] It is therefore an object of the present invention to provide monosheet direct thermal
imaging materials for labelling applications which do not fade.
[0009] It is therefore a further object of the present invention to provide substantially
light-insensitive monosheet direct thermal imaging materials for labelling applications
with excellent light stability and image tone.
[0010] Further objects and advantages of the invention will become apparent from the description
hereinafter.
Summary of the invention
[0011] It has been surprisingly found that labels produced using substantially light-insensitive
monosheet direct thermal imaging materials based on organic silver salts do not fade
and have excellent light stability and image tone.
[0012] The above-mentioned objects are realized by the use of a substantially light-insensitive
monosheet direct thermal imaging material for producing a non-retro-reflective readable
object attachable to a second object for information purposes, the imaging material
including a support, a thermosensitive element and an attaching layer, characterized
in that the thermosensitive element contains a substantially light-insensitive organic
silver salt, a reducing agent therefor in thermal working relationship therewith,
a binder and does not contain a di-or triarylmethane dye precursor compound possessing
within its di- or triarylmethane structure an aryl group substituted in the ortho
position to the meso carbon atom with an S-containing moiety ring-closed on the meso
carbon atom selected from a thiolactone, dithiolactone and thioether moiety.
[0013] Preferred embodiments of the present invention are disclosed in the detailed description
of the invention.
Detailed description of the invention.
Definitions
[0014] A label according to the present invention is a non-retro-reflective readable object
attachable to a second object for information purposes.
[0015] A direct thermal imaging material is a material in which coloration is obtained in
areas of the material to which heat is supplied either directly by an external heat
source or indirectly by heat produced upon absorption of infra-red radiation in these
areas of the material.
[0016] Transparent means capable of transmitting visible light without appreciable scattering.
[0017] By substantially light-insensitive is meant not intentionally light sensitive.
[0018] The descriptor aqueous in the term aqueous medium for the purposes of the present
invention includes mixtures of water-miscible organic solvents such as alcohols e.g.
methanol, ethanol, 2-propanol, butanol, iso-amyl alcohol etc.; glycols e.g. ethylene
glycol; glycerine; N-methyl pyrrolidone; methoxypropanol; and ketones e.g. 2-propanone
and 2-butanone etc. with water in which water constitutes more than 50% by weight
of the aqueous medium with 65% by weight of the aqueous medium being preferred and
80% by weight of the aqueous being particularly preferred.
[0019] The encapsulated organic silver salt in a heat-responsive microcapsule disclosed
in EP 736 799A whose use in the thermosensitive element of the present invention is
preferably excluded has a wall which isolates the substances incorporated therein
from the exterior at room temperature, but becomes permeable without being destroyed
when pressure is applied or when heated. The microcapsule can be prepared by any of
interfacial polymerization, internal polymerization and external polymerization. Interfacial
polymerization comprises emulsifying a core substance comprising an organic silver
salt that has been dissolved or dispersed in an organic solvent in an aqueous solution
having a water-soluble polymer therein and then forming a polymer wall around the
emulsified oil droplets of the core substance.
[0020] A leuco-dye is a colourless or weakly coloured compound derived from a dye. Colourless
or light coloured dye precursor leuco-dye systems whose use in the thermosensitive
element of the present invention is excluded include leuco triarylmethane, indolyl
phthalide, diphenylmethane, 2-anilinofluoran, 7-anilinofluoran, xanthene and spiro
compounds such as disclosed in EP-A 754 564.
[0021] By the term "heat solvent" in this invention is meant a non-hydrolyzable organic
material which is in a solid state in the recording layer at temperatures below 50°C,
but becomes a plasticizer for the recording layer when thermally heated and/or a liquid
solvent for the organic silver salt or the reducing agent.
Use of substantially light-insensitive monosheet direct thermal transparent imaging
materials containing an organic silver salt for the production of labels
[0022] It has been surprisingly found that the image-forming behaviour of substantially
light-insensitive monosheet direct thermal imaging materials based on organic silver
salts deviates from that of other substantially light-insensitive monosheet direct
thermal imaging materials in that the image density and image tone are critically
dependent upon the conditions applying during image formation as can be seen by comparing
COMPARATIVE EXAMPLES 1 to 11 with INVENTION EXAMPLES 12 to 33. Whereas in the widely
used leuco dye-containing imaging materials the image density did not vary systematically
with the heating energy applied to the adjacent heating element during the thermographic
development process, the so-called dot energy, the image density achieved with a substantially
light-insensitive monosheet direct thermal imaging material based on an organic silver
salt appears surprisingly mainly to depend upon the heating energy applied to the
adjacent heating element during the thermographic development process. Since dot energy
is the product of heating power and heating pulse-length, this implies that the image
density is surprisingly almost independent of the heating power. Moreover, the heating
power will largely determine the temperature attained by the heating element and hence
that attained by the substantially light-insensitive monosheet direct thermal imaging
material based on an organic silver salt in proximity to the heating element during
the thermal development process. This means that the image density is almost independent
of the temperature attained by the substantially light-insensitive monosheet direct
thermal imaging material based on an organic silver salt in proximity to the heating
element during the thermal development process. Furthermore this dot energy can be
supplied to one or more heating elements activated to produce the dot with a particular
image density i.e. the heating power (i.e. drive voltage squared divided by the heating
element resistance) applied to the one or more heating elements, in one or more heat
pulses and the duration of the one or more pulses.
[0023] Above a threshold energy, INVENTION EXAMPLES 1 to 11 show that the image density
increases with increasing dot energy up to a maximum image density. The dot energy
corresponding to this maximum image density has been found to be dependent upon the
choice of reducing agent for a particular organic silver salt, the choice of toning
agent and the ratio of binder to organic silver salt in the thermosensitive element.
At still higher energies the image density decreases with further increase in dot
energy. For a given binder to organic silver salt ratio and given concentration of
a particular reducing agent and toning agent, the image density potential of the material
has been found mainly to depend upon the weight per unit area of substantially light-insensitive
organic silver salt therein.
Substantially light-insensitive monosheet direct thermal transparent imaging materials
containing an organic silver salt for the production of labels
[0024] The substantially light-insensitive monosheet direct thermal imaging materials of
the present invention, includes a support, a thermosensitive element and an attaching
layer and in a preferred embodiment further includes a dyed or a pigmented transparent
layer to provide a coloured background for the image on the label. The dyed or the
pigmented transparent layer is preferably provided on the support. The substantially
light-insensitive monosheet direct thermal imaging material of the present invention
are preferably transparent.
[0025] The attaching layer is, once an optional protective foil has been removed, the outermost
layer on the same side of the support as the thermosensitive element or the outermost
layer on the side of the support not provided with the thermosensitive element. This
attaching layer provides adhesion upon contact with the surface of an object to which
it is to be attached under the conditions of attachment. This object is a solid whose
surface may, for example, be plastic, paper, metal, wood, glass, ceramic etc. Such
adhesion is a co-operative effect between the attaching layer and the surface of the
object to which it is attached and is influenced by the conditions of attachment.
Therefore the choice of attaching layer is dependent upon the surface of the object
to which it is to be attached, i.e. the absence of species such as particles, adsorbed
solvent or water, oxidized layers, grease etc. which would inhibit the adhesion process,
and the conditions under which attachment takes place e.g. the application of heat,
pressure, solvent etc. This attaching layer may, for example, be a single or multi-component,
cold, hot-melt or pressure resinous adhesive. The protective foil may, for example,
be plastic, metallic or a glassine-based paper coated e.g. with a silicone layer.
Thermosensitive element
[0026] The substantially light-insensitive monosheet direct thermal imaging material used
in the present invention comprises a thermosensitive element. The thermosensitive
element contains a substantially light-insensitive organic silver salt, a reducing
agent therefor in thermal working relationship therewith a binder and does not contain
a di-or triarylmethane dye precursor compound possessing within its di- or triarylmethane
structure an aryl group substituted in the ortho position to the meso carbon atom
with an S-containing moiety ring-closed on the meso carbon atom selected from a thiolactone,
dithiolactone and thioether moiety.
[0027] A di-or triarylmethane dye precursor compound possessing within its di- or triarylmethane
structure an aryl group substituted in the ortho position to the meso carbon atom
with an S-containing moiety ring-closed on the meso carbon atom selected from a thiolactone,
dithiolactone and thioether moiety is disclosed in WO 87/03541 and may be represented
by the formula

wherein X is -(C=O)-, -(C=S)- or -CH
2-; ring B represents a substituted or unsubstituted carbocyclic aryl ring or a heterocyclic
aryl ring; and Z and Z' taken individually represent the moieties; to complete the
auxochromophoric system of a diarylmethane or a triarylmethane dye when said S-containing
ring is open. Furthermore, this thermosensitive element preferably excludes colourless
or light coloured dye precursor leuco-dye systems and also preferably excludes encapsulated
organic silver salt in a heat-responsive microcapsule.
[0028] The thermosensitive element may also comprise a layer system in which the ingredients
may be dispersed in different layers, with the proviso that the substantially light-insensitive
organic silver salt and the reducing agent are in thermal working relationship with
one another i.e. during the thermal development process the reducing agent must be
present in such a way that it is able to diffuse to the substantially light-insensitive
organic silver salt particles so that reduction of the substantially light-insensitive
organic silver salt can take place.
Organic silver salts
[0029] Preferred substantially light-insensitive organic silver salts for use in the thermosensitive
element of the substantially light-insensitive monosheet direct thermal imaging material
used in 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,
which silver salts are also called "silver soaps". Combinations of different organic
silver salts may also be used in the imaging materials of the present invention.
Organic reducing agents
[0030] 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: catechol; hydroquinone; aminophenols;
METOL™; p-phenylenediamines; alkoxynaphthols, e.g. 4-methoxy-1-naphthol described
in US-P 3,094,417; pyrolidin-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.
[0031] The choice of reducing agent influences the thermal sensitivity of the imaging material
and the gradation of the image. Imaging materials using gallates, for example, have
a high gradation. In a preferred embodiment of the present invention the thermosensitive
element contains a 3,4-dihydroxyphenyl compound in which a benzene ring substituted
with any group in the 1-position is further substituted with hydroxy-groups in the
3- and 4-positions, the 3,4-dihydroxyphenyl compound being preferably selected from
the group consisting of gallic acid derivatives, gallates, ethyl 3,4-dihydroxybenzoate,
butyl 3,4-dihydroxybenzoate, 3,4-dihydroxy-benzoic acid and 3,4-dihydroxybenzonitrile.
In a particularly preferred embodiment the thermosensitive element further contains
a second reducing agent.
Binder
[0032] The thermosensitive element of the direct thermal transparent imaging material used
in the present invention may be coated onto a support in sheet- or web-form from an
organic solvent containing the binder dissolved therein or may be applied from an
aqueous medium using water-soluble or water-dispersible binders.
[0033] Suitable binders for coating from an organic solvent are all kinds of natural, modified
natural or synthetic resins or mixtures of such resins, wherein the organic heavy
metal salt can be dispersed homogeneously or mixtures thereof.
[0034] Suitable water-soluble film-forming binders are: polyvinyl alcohol, polyacrylamide,
polymethacrylamide, polyacrylic acid, polymethacrylic acid, polyethyleneglycol, polyvinylpyrrolidone,
proteinaceous binders such as gelatin modified gelatins such as phthaloyl gelatin,
polysaccharides, such as starch, gum arabic and dextrin and water-soluble cellulose
derivatives. Suitable water-dispersible binders are any water-insoluble polymer.
[0035] As the binder to organic silver salt weight ratio decreases the gradation of the
image increasing. Binder to organic silver salt weight ratios of 0.2 to 6 are preferred
with weight ratios between 0.5 and 3 being particularly preferred.
[0036] The above mentioned binders or mixtures thereof may be used in conjunction with waxes
or "heat solvents" to improve the reaction speed of the organic silver salt reduction
at elevated temperatures.
Toning agents
[0037] In order to obtain a neutral black image tone in the higher densities and neutral
grey in the lower densities, the direct thermal transparent imaging material used
in the present invention may contain one or more toning agents. The toning agents
should be in thermal working relationship with the substantially light-insensitive
organic silver salt and reducing agents during thermal processing. Any known toning
agent from thermography or photothermography may be used. Suitable toning agents are
the phthalimides and phthalazinones within the scope of the general formulae described
in US-P 4,082,901 and the toning agents described in US-P 3,074,809, US-P 3,446,648
and US-P 3,844,797. Particularly useful toning agents are the heterocyclic toner compounds
of the benzoxazine dione or naphthoxazine dione type described in GB-P 1,439,478,
US-P 3,951,660 and US-P 5,599,647.
Stabilizers and antifoggants
[0038] In order to obtain improved shelf-life and reduced fogging, stabilizers and antifoggants
may be incorporated into the substantially light-insensitive monosheet direct thermal
imaging material used in the present invention. Suitable stabilizers compounds for
use in the substantially light-insensitive monosheet direct thermal imaging material
used in the present invention are represented by general formula I :

where Q are the necessary atoms to form a 5- or 6-membered aromatic heterocyclic
ring, 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.
Surfactants and dispersants
[0039] Surfactants and dispersants aid the dispersion of ingredients which are insoluble
in the particular dispersion medium. The substantially light-insensitive monosheet
direct thermal imaging material used in the present invention may contain one or more
surfactants, which may be anionic, non-ionic or cationic surfactants and/or one or
more dispersants. Suitable dispersants are natural polymeric substances, synthetic
polymeric substances and finely divided powders, e.g. finely divided non-metallic
inorganic powders such as silica.
Other ingredients
[0040] In addition to the ingredients the direct thermal transparent imaging material may
contain other additives such as free fatty acids, 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, silica, and/or optical brightening
agents.
Support
[0041] The support of the direct thermal transparent imaging material used in the present
invention is transparent and is preferably a thin flexible carrier made transparent
resin film, e.g. made of a cellulose ester, e.g. cellulose triacetate, polypropylene,
polycarbonate or polyester, e.g. polyethylene terephthalate. The support may be in
sheet, ribbon or web form and subbed if needs be to improve the adherence to the thereon
coated thermosensitive element. The support may be dyed or pigmented to provide a
transparent coloured background for the image.
Protective layer
[0042] In a preferred embodiment of the present invention a protective layer is provided
for the thermosensitive element. In general this protects the thermosensitive element
from atmospheric humidity and from surface damage by scratching etc. and prevents
direct contact of printheads or heat sources with the recording layers. Protective
layers for thermosensitive elements which come into contact with and have to be transported
past a heat source under pressure, have to exhibit resistance to local deformation
and good slipping characteristics during transport past the heat source during heating.
A slipping layer, being the outermost layer, may comprise a dissolved lubricating
material and/or particulate material, e.g. talc particles, optionally protruding from
the outermost layer. Examples of suitable lubricating materials are a surface active
agent, a liquid lubricant, a solid lubricant or mixtures thereof, with or without
a polymeric binder.
Coating techniques
[0043] The coating of any layer of the substantially light-insensitive mainsheet direct
thermal transparent imaging material used in the present invention may proceed by
any known 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, USA. Coating may proceed from aqueous or
solvent media with overcoating of dried, partially dried or undried layers.
Thermographic printing
[0044] Direct thermal 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.
[0045] 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
into heat via Joule effect. The electric pulses thus converted into thermal signals
manifest themselves as heat transferred to the surface of the thermal paper wherein
the chemical reaction resulting in colour development 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 1.0ms, 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.
[0046] 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.
[0047] 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,
optionally linked to a digital image work station wherein the image information can
be processed to satisfy particular needs.
[0048] 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 pulsewise. When used in
thermographic recording operating with thermal printheads the imaging 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.
[0049] The following examples and comparative examples illustrate the present invention.
The percentages and ratios used in the examples are by weight unless otherwise indicated.
COMPARATIVE EXAMPLES 1 to 11
Leuco-dye based direct thermal imaging material for label production
[0050] The label-printing apparatus used for these experiments was a thermal head printer,
the thermal head having a nominal resistance of 102.6 ohms and 115µm by 142µm heating
elements. It printed with a line time of 11.5ms at a process speed of 7.3mm/s, was
powered by six 1.5 volt batteries and had a DC-motor driven drum transport.
[0051] BROTHER P-TOUCH TYPE™ M-K231 black on white leuco-dye-based direct thermal imaging
material with an opaque white backing layer was printed with three heating pulses
evenly distributed over the line time at the voltages and pulse times given in table
1. The image density D
vis and the CIELAB L*, a* and b* values determined in refection according to ASTM Norm
E308 of the resulting prints are given in table 1 below.
Table 1
| Comparative example nr |
Printing conditions |
Print characteristics |
| |
dot energy [mJ/mm2] |
printhead voltage [V] |
pulse-length [ms] |
Dvis |
L* |
a* |
b* |
| 1 |
49.2 |
3.95 |
1.76 |
1.51 |
20.39 |
-0.10 |
-5.03 |
| 2 |
55.6 |
4.20 |
1.76 |
1.57 |
18.88 |
0.89 |
-5.36 |
| 3 |
56.2 |
3.95 |
2.01 |
1.51 |
20.33 |
0.73 |
-5.63 |
| 4 |
63.5 |
4.20 |
2.01 |
1.57 |
18.81 |
0.81 |
-5.06 |
| 5 |
64.2 |
3.95 |
2.30 |
1.55 |
19.37 |
0.61 |
-5.33 |
| 6 |
68.2 |
4.65 |
1.76 |
1.58 |
18.41 |
0.73 |
-4.79 |
| 7 |
72.6 |
4.20 |
2.30 |
1.60 |
17.97 |
0.72 |
-4.64 |
| 8 |
77.8 |
4.65 |
2.01 |
1.59 |
18.31 |
0.45 |
-4.53 |
| 9 |
83.4 |
4.20 |
2.64 |
1.56 |
19.04 |
0.33 |
-4.58 |
| 10 |
89.0 |
4.65 |
2.30 |
1.58 |
18.39 |
0.28 |
-4.75 |
| 11 |
95.4 |
4.20 |
3.02 |
1.65 |
16.73 |
0.42 |
-3.80 |
| 12 |
102.2 |
4.65 |
2.64 |
1.60 |
17.86 |
0.60 |
-4.70 |
| 13 |
109.3 |
4.20 |
3.46 |
1.65 |
16.81 |
-0.01 |
-3.38 |
| 14 |
116.9 |
4.65 |
3.02 |
1.65 |
16.73 |
0.49 |
-4.26 |
| 15 |
134.0 |
4.65 |
3.46 |
1.64 |
16.99 |
0.45 |
-4.70 |
[0052] These results show a possible marginal increase in D
vis and no significant dependence of a*- and b*-values upon dot energy.
Exposure of prints to artificial sunlight in a lightfastness test
[0053] The lightfastness of a print produced with the BROTHER P-TOUCH TYPE™ M-K231 leuco
dye-based direct thermal imaging material was evaluated according to DIN 54 024 of
August 1983 for the determination of lightfastness of colourings and prints, which
is equivalent to the ISO-document 38/l N 767, pages 59-73, with an Atlas Material
Testing Technology By, D-63558 Gelnhausen, Germany, SUNTEST™ CPS apparatus. In this
test the print is exposed to artificial sunlight through a glass filter together with
standardized pigmented cloth samples and exposed to different doses of artificial
sunlight as determined by the fading of the standardized pigmented cloth samples and
expressed as numbers on the International Wool-scale. The background density, D
min, maximum density, D
max, and CIELAB a*- and b*-values of the black print with respect to the white background
of the material determined after exposure to different International Wool-scale exposures
are summarized in table 2.
Table 2
| |
Dmax |
a* |
b* |
Dmin |
a* |
b* |
| Image characteristics prior to sunlight exposure |
1.602 |
2.21 |
-6.78 |
0.083 |
-1.72 |
3.31 |
| Image characteristics after an exposure of 2 according to the IWS* |
1.591 |
2.04 |
-7.08 |
0.087 |
-1.40 |
4.35 |
| Image characteristics after an exposure of 4 according to the IWS* |
1.558 |
2.92 |
-7.59 |
0.096 |
-0.92 |
10.23 |
| Image characteristics after an exposure of 5 according to the IWS* |
1.040 |
18.73 |
-4.33 |
0.144 |
1.00 |
24.29 |
| Image characteristics after an exposure of 5+ according to the IWS* |
1.116 |
16.37 |
-2.06 |
0.146 |
1.06 |
24.74 |
| * International Wool-scale |
[0054] From table 2 it is evident that at exposures below 6 on the International Wool-scale,
there is an appreciable decrease in D
max associated with a strong increase in its CIELAB a*-value indicating a shift in the
image tone in reflection to the red, which is visible as an increasingly brown image
tone, and an increase in D
min associated with a strong increase in its CIELAB b*-value, indicating a shift in the
image tone of the background to the yellow.
INVENTION EXAMPLES 1 to 11
Preparation of the thermosensitive element
[0055] The subbed 63µm thick polyethylene terephthalate support was doctor blade-coated
with a composition containing 2-butanone as solvent/dispersing medium so as to obtain
thereon, after drying for 1 hour at 50°C, a thermosensitive element with the composition:

Overcoating of thermosensitive element with a protective layer
[0056] The above-described thermosensitive element was overcoated with a protective layer
with the composition:
| PIOLOFORM™ LL4160, a polyvinyl butyral from WACKER CHEMIE |
1.539 g/m2 |
| BAYSILON™ MA, a silicone oil from BAYER |
0.006 g/m2 |
| MICRODOL™ SUPER, a talc from Norwegian Talc AS |
0.052 g/m2 |
| TINUVIN™ 320 from CIBA-GEIGY |
0.229 g/m2 |
| TEGOGLIDE™ 410 from Goldschmidt |
0.02 g/m2 |
| DESMODUR™ N100, a hexamethylene diisocyanate from BAYER |
0.154 g/m2 |
Thermographic printing
[0057] The thermographic printer used in these experiments was also a thermal head printer,
but had a thermal head with a nominal resistance of 1850 ohms, had 85µm by 85µm heating
elements, printed with a line time of 11.5ms and the thermographic material was transported
at a process speed of 7.36 mm/s. The number of heating pulses, printhead voltages
and pulse times were completely variable.
[0058] The above-described direct thermal material was printed with a single pulse per line
time and at the voltages and pulse times given in table 3 below. The image density
D
vis and the CIELAB L*, a* and b* values determined in refection according to ASTM Norm
E308 of the resulting prints are given in table 3 below.
[0059] The experiments of INVENTION EXAMPLES 1 to 11 show an increase in image density D
vis with increasing dot energy. However, the D
vis value appears to stabilize and then decrease at the highest dot energies used. The
L* value, a measure of the transmission of the layer decreases with increasing dot
energy consistent with the increase in D
vis.
Table 3
| Invention example number |
Printing conditions |
Print characteristics |
| |
dot energy [mJ/mm2] |
printhead voltage [V] |
pulse-length [ms] |
Dvis |
L* |
a* |
b* |
| 1 |
37.9 |
11.5 |
3.83 |
0.01 |
99.23 |
-0.04 |
0.92 |
| 2 |
41.7 |
11.5 |
4.21 |
0.06 |
94.84 |
0.18 |
2.37 |
| 3 |
45.5 |
11.5 |
4.60 |
0.22 |
81.73 |
0.62 |
6.02 |
| 4 |
49.3 |
11.5 |
4.98 |
0.52 |
61.90 |
0.98 |
9.34 |
| 5 |
53.0 |
11.5 |
5.36 |
0.90 |
41.99 |
1.70 |
11.15 |
| 6 |
56.9 |
11.5 |
5.75 |
1.42 |
22.89 |
2.89 |
9.70 |
| 7 |
60.6 |
11.5 |
6.13 |
1.79 |
13.34 |
2.90 |
4.69 |
| 8 |
64.4 |
11.5 |
6.51 |
1.86 |
11.79 |
1.69 |
0.33 |
| 9 |
68.2 |
11.5 |
6.89 |
1.98 |
9.44 |
1.13 |
-1.37 |
| 10 |
72.0 |
11.5 |
7.28 |
1.98 |
9.43 |
0.95 |
-1.35 |
| 11 |
75.8 |
11.5 |
7.66 |
1.89 |
11.20 |
0.76 |
-2.00 |
[0060] Colour neutrality on the basis of CIELAB-values corresponds to a* and b* values of
zero, with a negative a*-value indicating a greenish image-tone becoming greener as
a* becomes more negative, a positive a*-value indicating a reddish image-tone becoming
redder as a* becomes more positive, a negative b*-value indicating a bluish image-tone
becoming bluer as b* becomes more negative and a positive b*-value indicating a yellowish
image-tone becoming more yellow as b* becomes more positive.
[0061] The decrease in a* and b* values with increasing dot energy to values near zero for
the highest dot energies used thus indicates that the image became more neutral with
increasing dot energy.
INVENTION EXAMPLES 12 to 33
Direct thermal transparent imaging material
[0062] The direct thermal transparent imaging material used in the experiments of INVENTION
EXAMPLES 12 to 33 was produced by coating the thermosensitive element overcoated with
a protective layer used in INVENTION EXAMPLES 1 to 11 and coating the opposite side
of the support to that coated with the thermosensitive element and its protective
layer sequentially with a 5.5g/m
2 coating of a white acrylic water-based ink pigmented with titanium dioxide having
an optical density of 0.38 and overcoating with a white pressure sensitive water-based
dispersion to a coating weight of 26g/m
2, the two layers together having an optical density of 0.65. The second layer was
then pressure laminated with the silicone-coated side of 65g/m
2 glassine-based paper coated with a silicone layer, which acts as a release foil.
Printing with a thermographic label-printing apparatus
[0063] The label-printing apparatus used for the printing experiments of COMPARATIVE EXAMPLES
1 to 11 was used in the printing experiments of INVENTION EXAMPLES 12 to 33 in which
a direct thermal transparent imaging material produced as described above was printed
with three heating pulses evenly distributed over the line time at the voltages and
pulse times given in table 4. The image density D
vis and the CIELAB L*, a* and b* values determined in refection according to ASTM Norm
E308 of the resulting prints are given in table 4 below.
[0064] The results are arranged in the order of the dot energies used, independent of the
heating power (quadratically dependent upon printhead voltage) and therefore of the
temperature attained by the heating element and hence that obtained by the material
local thereto. These results are surprising in two ways: in contrast to INVENTION
EXAMPLES 1 to 11, the image density decreased with increase dot energy and furthermore
despite considerable variations in temperature during the thermal development process
due to the different heating powers used in the experiments of INVENTION EXAMPLES
12 to 33, the image density, D
vis, was found to be mainly dependent upon the dot energy applied, decreasing with increasing
dot energy.
[0065] Furthermore, L*, a* and b* were also found to be dependent upon the dot energy, L*
increasing with increasing dot energy, indicating decreasing optical density, and
a* and b* increasing with increasing dot energy from values in the region of zero
indicating colour neutrality at lower dot energies to increasingly less neutral colour
tone with increasing dot energy.
Table 4
| Invention example number |
Printing conditions |
Print characteristics |
| |
dot energy [mJ/mm2] |
printhead voltage [V] |
pulse-length [ms] |
Dvis |
L* |
a* |
b* |
| 12 |
63.7 |
4.20 |
1.76 |
1.93 |
10.39 |
-0.04 |
3.87 |
| 13 |
72.3 |
4.20 |
2.01 |
2.15 |
6.34 |
0.81 |
-0.98 |
| 14 |
77.8 |
4.65 |
1.76 |
1.97 |
9.54 |
1.70 |
-0.14 |
| 15 |
82.7 |
4.20 |
2.30 |
1.95 |
9.98 |
1.02 |
-0.62 |
| 16 |
88.8 |
4.65 |
2.01 |
1.77 |
13.88 |
3.45 |
1.26 |
| 17 |
94.9 |
4.20 |
2.64 |
1.74 |
14.46 |
2.98 |
1.27 |
| 18 |
97.4 |
5.20 |
1.76 |
1.65 |
16.64 |
8.89 |
5.00 |
| 19 |
101.7 |
4.65 |
2.30 |
1.60 |
18.00 |
6.05 |
3.53 |
| 20 |
109.0 |
4.20 |
3.02 |
1.64 |
16.90 |
9.95 |
7.09 |
| 21 |
110.8 |
5.20 |
2.01 |
1.52 |
20.17 |
10.38 |
6.89 |
| 22 |
116.4 |
4.65 |
2.64 |
1.49 |
20.97 |
11.56 |
7.56 |
| 23 |
124.9 |
4.20 |
3.46 |
1.58 |
18.52 |
16.04 |
13.45 |
| 24 |
127.4 |
5.20 |
2.30 |
1.50 |
20.59 |
19.18 |
14.52 |
| 25 |
133.5 |
4.65 |
3.02 |
1.50 |
20.71 |
18.20 |
14.52 |
| 26 |
136.6 |
5.20 |
2.47 |
1.41 |
23.42 |
18.00 |
12.76 |
| 27 |
145.7 |
5.20 |
2.64 |
1.25 |
28.30 |
17.29 |
9.70 |
| 28 |
153.1 |
4.65 |
3.46 |
1.36 |
24.83 |
18.14 |
12.07 |
| 29 |
155.5 |
5.20 |
2.82 |
1.23 |
29.00 |
20.77 |
12.14 |
| 30 |
167.2 |
5.20 |
3.02 |
1.13 |
32.84 |
14.02 |
9.14 |
| 31 |
178.2 |
5.20 |
3.23 |
1.00 |
37.69 |
13.86 |
13.27 |
| 32 |
191.1 |
5.20 |
3.46 |
0.95 |
39.80 |
13.06 |
11.07 |
| 33 |
204.5 |
5.20 |
3.70 |
0.86 |
43.94 |
11.81 |
17.49 |
Exposure of prints to artificial sunlight in a lightfastness test
[0066] A print produced with the organic silver salt-containing thermographic material was
exposed to artificial sunlight through a glass filter in an Atlas Material Testing
Technology BV, SUNTEST™ CPS apparatus according to DIN 54 004. The changes in the
background density, D
min, the maximum density, D
max, and CIELAB a*-and b*-values with respect to the white background of the material
expressed in terms of particular UV-light doses expressed as numbers on the International
Woolscale are summarized in table 5.
Table 5
| |
Dmax |
a* |
b* |
Dmin |
a* |
b* |
| Image characteristics prior to sunlight exposure |
1.805 |
12.87 |
4.42 |
0.109 |
-0.90 |
9.67 |
| Image characteristics after an exposure of 4 according to the IWS* |
1.862 |
11.26 |
2.88 |
0.139 |
-0.51 |
10.34 |
| Image characteristics after an exposure of 7 according to the IWS* |
1.845 |
11.92 |
2.61 |
0.167 |
0.85 |
16.26 |
| * International Wool-scale |
[0067] From table 5 it is evident that even at exposures of 7 on the International Wool-scale,
there is no significant change in D
max or its CIELAB a*- and b*-values, i.e. there is no fading or changes in the image
tone, and the increase in D
min is appreciably lower and the increase in its CIELAB b*-value much less pronounced
than in the case of the BROTHER P-TOUCH TYPE™ M-K231 leuco dye-based direct thermal
imaging material.
[0068] This demonstrates that using thermographic materials based upon organic silver salts
have the advantages over the conventionally used leuco dye-based direct thermal imaging
materials of no fading or changes in the image tone in D
max and reduced D
min increase and background discoloration upon exposure to artificial sunlight.
[0069] 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.