[0001] This invention relates to a laser recording element, and more particularly to a single-sheet
laser recording element wherein the support is a microvoided composite film.
[0002] In recent years, thermal transfer systems have been developed to obtain prints from
pictures which have been generated electronically from a color video camera. According
to one way of obtaining such prints, an electronic picture is first subjected to color
separation by color filters. The respective color-separated images are then converted
into electrical signals. These signals are then operated on to produce cyan, magenta
and yellow electrical signals. These signals are then transmitted to a thermal printer.
To obtain the print, a cyan, magenta or yellow dye-donor element is placed face-to-face
with a dye-receiving element. The two are then inserted between a thermal printing
head and a platen roller. A line-type thermal printing head is used to apply heat
from the back of the dye-donor sheet. The thermal printing head has many heating elements
and is heated up sequentially in response to the cyan, magenta and yellow signals.
The process is then repeated for the other two colors. A color hard copy is thus obtained
which corresponds to the original picture viewed on a screen.
[0003] U.S. Patent No. 5,244,861 relates a receiving element useful in the above-described
thermal dye transfer process which contains a microvoided composite film as the support.
There is no disclosure in this patent that the support would be useful in other thermal
systems.
[0004] Another way to thermally obtain a print using the electronic signals described above
is to use a laser instead of a thermal printing head. In such a laser transfer system,
the donor sheet includes a material which strongly absorbs at the wavelength of the
laser. When the donor is irradiated, this absorbing material converts light energy
to thermal energy and transfers the heat to the dye in the immediate vicinity, thereby
heating the dye to its vaporization temperature for transfer to a receiver. The absorbing
material may be present in a layer beneath the dye and/or it may be admixed with the
dye. The laser beam is modulated by electronic signals which are representative of
the shape and color of the original image, so that each dye is heated to cause volatilization
only in those areas in which its presence is required on the receiver to reconstruct
the color of the original object. Further details of this process are found in GB
2,083,726A.
[0005] In another mode of imaging using a laser beam, a laser recording element with a dye
layer composition comprising an image dye, an infrared-absorbing material, and a binder
coated onto a substrate is imaged from the dye side. The energy provided by the laser
drives off the image dye and other components of the dye layer at the spot where the
laser beam impinges upon the element. In "laser removal" imaging, the laser radiation
causes rapid local changes in the imaging layer, thereby causing the material to be
removed from the layer. Usefulness of such a laser recording element is largely determined
by the efficiency at which the imaging dye can be removed on laser exposure. The transmission
Dmin value is a quantitative measure of dye clean-out: the lower its value at the
recording spot, the more complete is the attained dye removal.
[0006] U.S. Patent No. 5,330,876 relates to a dye ablative recording element as described
above. The element comprises a support having thereon a dye layer containing an image
dye, IR-absorbing dye and binder. The element is imagewise-exposed by a laser and
portions of the dye layer are ablated away to produce a dye image. The support for
this element is the conventional supports used in this field.
[0007] There is a problem with the above dye ablative recording elements in that the minimum
density and speed are not as good as is desired.
[0008] It is an object of this invention to provide a dye ablative recording element wherein
the minimum density and speed are improved over that of the prior art. It is another
object of this invention to provide a process for forming an image using this recording
element.
[0009] These and other objects are achieved in accordance with the invention which relates
to a laser recording element comprising a base having thereon a dye layer comprising
an image dye dispersed in a polymeric binder, the dye layer having an infrared-absorbing
material associated therewith, the base comprising a composite film laminated to at
least one side of a support, the dye layer being on the composite film side of the
base, and the composite film comprising a microvoided thermoplastic core layer and
at least one substantially void-free thermoplastic surface layer.
[0010] Any visible image dye can be used in the laser recording element employed in the
invention provided it can be removed by the action of the laser. Especially good results
have been obtained with dyes such as

or any of the dyes disclosed in U.S. Patents 4,541,830, 4,698,651, 4,695,287, 4,701,439,
4,757,046, 4,743,582, 4,769,360, and 4,753,922. The above dyes may be employed singly
or in combination. The dyes may be used at a coverage of from about 0.05 to about
1 g/m
2 and are preferably hydrophobic.
[0011] Another embodiment of the invention relates to a process of forming a dye image comprising
imagewise-heating, by means of a laser, the recording element described above, the
laser exposure taking place through the dye side of the element and causing dye to
be removed imagewise to obtain the dye image in the recording element.
[0012] In still another preferred embodiment of the invention, dye is removed imagewise
by means of an air stream, vacuum and filter system.
[0013] The laser recording elements of this invention can be used to obtain medical images,
reprographic masks, printing masks, etc. The image obtained can be a positive or a
negative image. The dye removal process can generate either continuous (photographic-like)
or halftone images.
[0014] Any polymeric material may be used as the binder in the recording element employed
in the invention. For example, there may be used cellulosic derivatives, e.g., cellulose
nitrate, cellulose acetate hydrogen phthalate, cellulose acetate, cellulose acetate
propionate, cellulose acetate butyrate, cellulose triacetate, a hydroxypropyl cellulose
ether, an ethyl cellulose ether, etc., polycarbonates; polyurethanes; polyesters;
poly(vinyl acetate); polystyrene; poly(styrene-co-acrylonitrile); a polysulfone; a
poly(phenylene oxide); a poly(ethylene oxide); a poly(vinyl alcohol-co-acetal) such
as poly(vinyl acetal), poly(vinyl alcohol-co-butyral) or poly(vinyl benzal); or mixtures
or copolymers thereof. The binder may be used at a coverage of from about 0.1 to about
5 g/m
2.
[0015] In a preferred embodiment, the polymeric binder used in the recording element employed
in the process of the invention has a polystyrene equivalent molecular weight of at
least 100,000 as measured by size exclusion chromatography, as described in U.S. Patent
5,330,876.
[0016] A barrier layer may be employed in the laser recording element of the invention if
desired, as described in U.S. Patent 5,459,017.
[0017] To obtain a laser-induced image according to the invention, a diode laser is preferably
employed, such as an infrared diode laser, since it offers substantial advantages
in terms of its small size, low cost, stability, reliability, ruggedness, and ease
of modulation. In practice, before an infrared laser can be used to heat a recording
element, the element must contain an infrared-absorbing material, such as cyanine
infrared-absorbing dyes as described in U.S. Patent 5,401,618 or other materials as
described in the following U.S. Patent Numbers: 4,948,777, 4,950,640, 4,950,639, 4,948,776,
4,948,778, 4,942,141, 4,952,552, 5,036,040, and 4,912,083. The laser radiation is
then absorbed into the dye layer and converted to heat by a molecular process known
as internal conversion. Thus, the construction of a useful dye layer will depend not
only on the hue, transferability and intensity of the image dyes, but also on the
ability of the dye layer to absorb the radiation and convert it to heat. The infrared-absorbing
dye may be contained in the dye layer itself or in a separate layer associated therewith,
i.e., above or below the dye layer. Preferably, the laser exposure in the process
of the invention takes place through the dye side of the recording element, which
enables this process to be a single-sheet process, i.e., a separate receiving element
is not required.
[0018] The dye layer of the laser recording element of the invention may be coated on the
support or printed thereon by a printing technique such as a gravure process or a
hopper coater.
[0019] Due to their relatively low cost and good appearance, composite films are generally
used and referred to in the trade as "packaging films." The support may include cellulose
paper, a polymeric film or a synthetic paper.
[0020] Unlike synthetic paper materials, microvoided packaging films can be laminated to
one side of most supports and still show excellent curl performance. Curl performance
can be controlled by the beam strength of the support. As the thickness of a support
decreases, so does the beam strength. These films can be laminated on one side of
supports of fairly low thickness/beam strength and still exhibit only minimal curl.
[0021] Microvoided composite packaging films are conveniently manufactured by coextrusion
of the core and surface layers, followed by biaxial orientation, whereby voids are
formed around void-initiating material contained in the core layer. Such composite
films are disclosed in, for example, U.S. Patent 5,244,861.
[0022] The core of the composite film should be from 15 to 95% of the total thickness of
the film, preferably from 30 to 85% of the total thickness. The nonvoided skin(s)
should thus be from 5 to 85% of the film, preferably from 15 to 70% of the thickness.
The density (specific gravity) of the composite film should be between 0.2 and 1.0
g/cm
3, preferably between 0.3 and 0.7 g/cm
3. As the core thickness becomes less than 30% or as the specific gravity is increased
above 0.7 g/cm
3, the composite film starts to lose useful compressibility and thermal insulating
properties. As the core thickness is increased above 85% or as the specific gravity
becomes less than 0.3 g/cm
3, the composite film becomes less manufacturable due to a drop in tensile strength
and it becomes more susceptible to physical damage. The total thickness of the composite
film can range from 20 to 150 µm, preferably from 30 to 70 µm. Below 30 µm, the microvoided
films may not be thick enough to minimize any inherent non-planarity in the support
and would be more difficult to manufacture. At thicknesses higher than 70 µm, little
improvement in either print uniformity or thermal efficiency is seen; and so there
is not much justification for the further increase in cost for extra materials.
[0023] Suitable classes of thermoplastic polymers for the core matrix-polymer of the composite
film include polyolefins, polyesters, polyamides, polycarbonates, cellulosic esters,
polystyrene, polyvinyl resins, polysulfonamides, polyethers, polyimides, poly(vinylidene
fluoride), polyurethanes, poly(phenylene sulfides), polytetrafluoroethylene, polyacetals,
polysulfonates, polyester ionomers, and polyolefin ionomers. Copolymers and/or mixtures
of these polymers can be used.
[0024] Suitable polyolefins include polypropylene, polyethylene, polymethylpentene, and
mixtures thereof. Polyolefin copolymers, including copolymers of ethylene and propylene
are also useful.
[0025] The composite film can be made with skin(s) of the same polymeric material as the
core matrix, or it can be made with skin(s) of polymeric composition different from
that of the core matrix. For compatibility, an auxiliary layer can be used to promote
adhesion of the skin layer to the core.
[0026] Addenda may be added to the core matrix to improve the whiteness of these films.
This would include any process which is known in the art including adding a white
pigment, such as titanium dioxide, barium sulfate, clay, or calcium carbonate. This
would also include adding optical brighteners or fluorescing agents which absorb energy
in the UV region and emit light largely in the blue region, or other additives which
would improve the physical properties of the film or the manufacturability of the
film.
[0027] Coextrusion, quenching, orienting, and heat setting of these composite films may
be effected by any process which is known in the art for producing oriented film,
such as by a flat film process or by a bubble or tubular process. The flat film process
involves extruding the blend through a slit die and rapidly quenching the extruded
web upon a chilled casting drum so that the core matrix polymer component of the film
and the skin components(s) are quenched below their glass transition temperatures
(Tg). The quenched film is then biaxially oriented by stretching in mutually perpendicular
directions at a temperature above the glass transition temperature of the matrix polymers
and the skin polymers. The film may be stretched in one direction and then in a second
direction or may be simultaneously stretched in both directions. After the film has
been stretched it is heat set by heating to a temperature sufficient to crystallize
the polymers while restraining the film to some degree against retraction in both
directions of stretching.
[0028] By having at least one nonvoided skin on the microvoided core, the tensile strength
of the film is increased and makes it more manufacturable. It allows the films to
be made at wider widths and higher draw ratios than when films are made with all layers
voided. Coextruding the layers further simplifies the manufacturing process.
[0029] The support to which the microvoided composite films are laminated for the base of
the recording element of the invention may be a polymeric, synthetic paper, or cellulose
fiber paper support, or laminates thereof.
[0030] Preferred cellulose fiber paper supports include those disclosed in U.S. Patent 5,250,496.
When using a cellulose fiber paper support, it is preferable to extrusion laminate
the microvoided composite films using a polyolefin resin. During the lamination process,
it is desirable to maintain minimal tension of the microvoided packaging film in order
to minimize curl in the resulting laminated support. The backside of the paper support
(i.e., the side opposite to the microvoided composite film) may also be extrusion
coated with a polyolefin resin layer (e.g., from about 10 to 75 g/m
2), and may also include a backing layer such as those disclosed in U.S. Patents 5,011,814
and 5,096,875. For high humidity applications (>50% RH), it is desirable to provide
a backside resin coverage of from about 30 to about 75 g/m
2, more preferably from 35 to 50 g/m
2, to keep curl to a minimum.
[0031] In one preferred embodiment, in order to produce recording elements with a desirable
photographic look and feel, it is preferable to use relatively thick paper supports
(e.g., at least 120 µm thick, preferably from 120 to 250 µm thick) and relatively
thin microvoided composite packaging films (e.g., less than 50 µm thick, preferably
from 20 to 50 µm thick, more preferably from 30 to 50 µm thick).
[0032] In another embodiment of the invention, in order to form a recording element which
resembles plain paper, e.g. for inclusion in a printed multiple page document, relatively
thin paper or polymeric supports (e.g., less than 80 µm, preferably from 25 to 80
µm thick) may be used in combination with relatively thin microvoided composite packaging
films (e.g., less than 50 µm thick, preferably from 20 to 50 µm thick, more preferably
from 30 to 50 µm thick).
[0033] The following example is provided to further illustrate the invention.
Example
Preparation of the Microvoided Support-Support A
[0034] A commercially available packaging film (OPPalyte® 350 TW, Mobil Chemical Co.) was
laminated to a paper support. OPPalyte® 350 TW is a composite film (38 µm thick) (d=0.62)
consisting of a microvoided and oriented polypropylene core (approximately 73% of
the total film thickness), with a titanium dioxide pigmented, non-microvoided, oriented
polypropylene layer on each side; the void-initiating material is poly(butylene terephthalate).
[0035] Packaging films may be laminated in a variety of way (by extrusion, pressure, or
other means) to a paper support. In the present context, they were extrusion-laminated
as described below with pigmented polyolefin onto a paper stock support. The pigmented
polyolefin was polyethylene (12 g/m
2) containing anatase (titanium dioxide) (12.5% by weight) and a benzoxazole optical
brightener (0.05% by weight).
[0036] The paper stock support was 137 µm thick and made form a 1:1 blend of Pontiac Maple
51 (a bleached maple hardwood kraft of 0.5 µm length weighted average fiber length),
available from Consolidated Pontiac, Inc., and Alpha Hardwood Sulfite (a bleached
red-alder hardwood sulfite of 0.69 µm average fiber length), available form Weyerhauser
Paper Co. The backside of the paper stock support was coated with high-density polyethylene
(30 g/m
2).
Preparation of the Non-Microvoided Support-Support B, (Control)
[0037] A non-microvoided support was prepared by extrusion-coating a pigmented polyolefin
unto a paper stock support. The pigmented polyolefin was polyethylene (12 g/m
2) containing anatase (titanium dioxide) (12.5% by weight) and a benzoxazole optical
brightener (0.05% by weight). The paper stock support was the same as described above.
The backside of the paper stock support was coated with high-density polyethylene
(30 g/m
2).
Laser Dye Ablation Layer
[0038] The following mixture was prepared and stirred until dissolved:
12 g nitrocellulose (Hercules)
0.24 g IR-1
0.24 g of cyan-2 dye illustrated above
70 g acetone

Element 1
[0039] The above solution was coated at 34 g/m
2, wet coverage, on paper Support A as described above.
Control 1
[0040] This is similar to Element 1 except that Support B was used instead of Support A.
Laser Exposure
[0041] After drying, the elements were exposed using Spectra Diode Labs Lasers Model SDL-2432,
with a maximum power of 600 mW per laser beam, at 830 nm, 1000 rev/min and a spot
size of approximately 12 µm x 25 µm using a lathe type printer with a drum circumference
of 53 cm. The diode laser beams were scanned across the surface of the element to
achieve 945 lines per cm, or 2400 lines per in. An air stream was blown over the donor
surface along with a vacuum and a filter system to remove the ablated material.
[0042] A step tablet image was printed by reducing the laser intensity linearly in successive
patches from the maximum to 0. Reflection Status A red densities were measured using
an X-Rite Model 310 reflection densitometer.
[0043] Readings were referenced to the uncoated paper support, respectively. The results
are given in the following Table. The closely matched D-max values indicate that the
coating thicknesses were the same within experimental error as intended (step 21).
Table
Step |
Laser Power (mW) |
Exposure (mJ/cm2) |
Element 1 |
Control 1 |
1 |
600 |
643 |
0.12 |
0.21 |
2 |
585 |
627 |
0.12 |
0.21 |
3 |
570 |
611 |
0.12 |
0.21 |
4 |
555 |
595 |
0.12 |
0.21 |
5 |
540 |
578 |
0.12 |
0.21 |
6 |
525 |
562 |
0.13 |
0.23 |
7 |
510 |
546 |
0.13 |
0.24 |
8 |
495 |
530 |
0.13 |
0.25 |
9 |
480 |
514 |
0.14 |
0.26 |
10 |
465 |
498 |
0.15 |
0.26 |
11 |
450 |
482 |
0.15 |
0.30 |
12 |
435 |
466 |
0.16 |
0.32 |
13 |
420 |
450 |
0.17 |
0.35 |
14 |
405 |
434 |
0.19 |
0.38 |
15 |
390 |
418 |
0.22 |
0.40 |
16 |
375 |
402 |
0.25 |
0.44 |
17 |
360 |
386 |
0.31 |
0.50 |
18 |
345 |
370 |
0.34 |
0.55 |
19 |
330 |
354 |
0.43 |
0.59 |
20 |
315 |
337 |
0.53 |
0.67 |
21 |
0 |
0 |
0.76 |
0.77 |
[0044] The above results show the element with the microvoided support (Element 1) was more
efficient, exhibiting a considerably lower D-min (Steps 1-5), than Control 1 which
used a non-microvoided support. The microvoided support also gave a speed improvement
which can be seen in the data by defining a speed point as the exposure required to
print to 0.03 above D-min (step 10 for Element 1 and step 7 for Control 1). The speed
point for Element 1 was 498 mJ/cm
2, while the speed point for Control 1 was 546 mJ/cm
2. Thus, Element 1 requires 9% less exposure to achieve this speed point.