FIELD OF THE INVENTION
[0001] This invention relates to thermal transfer printing, and in particular to a novel
thermal transfer receptor sheet for such printing using a coated metallized-polymer
surface as a receptor surface.
BACKGROUND OF THE INVENTION
[0002] In thermal dye transfer printing, an image is formed on a receptor sheet by selectively
transferring a dye to a receptor sheet from a dye donor sheet placed in momentary
contact with the receptor sheet. Material to be transferred from the dye donor sheet
is directed by a thermal printhead, which consists of small electrically heated elements
(print heads). These elements transfer image-forming material from the dye donor sheet
to areas of the dye receptor sheet in a image-wise manner. Thermal dye transfer systems
have advantages over other thermal transfer systems, such as chemical reaction systems,
and thermal mass transfer systems. In general thermal dye transfer systems offer greater
control of gray scale than these other systems, but they have problems as well. One
problem is release of the dye donor and receptor layers during printing. This has
been addressed often by the addition of dye-permeable release coatings applied to
the surface of the dye receptor layer. Additionally, materials are required for use
in the receptor layer having suitable dye permeability, mordanting properties, adhesion
to the substrate, and long term light and thermal stability.
[0003] It is often desirable for imaging systems to be useful on different types of receptor
substrates. This is particularly true in imaging systems used in proofing operations
where the final image is to give the appearance of the final printed product. Where
the final product is to be an image provided on a metal surface, it is difficult for
may types of proofing systems to provide a realistic imaging system. Conventional
photomechanical proofing systems which operate by using specialized photoresist or
phototackifiable elements can not readily provide quality images on metal surfaces
as they are not designed for such image productions.
[0004] Thermal dye transfer and thermal mass transfer often require special receptor surfaces
to provide the highest quality images. Thermal mass transfer has been able to provide
fairly accurate renditions of images on metallized surfaces by first transfering a
metallic thermal mass transfer background and then transfering a colored image on
top of or within the borders of the metallic image. Thermal dye transfer can not perform
that type of two step image transfer because metallic appearing images or backgrounds
are not readily provided by dyes or dye-like materials susceptible to the thermal
dye transfer process.
[0005] Recent advances in thermal dye transfer imaging systems describe thermal dye transfer
receptor layers which can be coated out of solution and used on various surfaces to
provide a high quality dye receiving layer. Such materials are described in U.S. Patent
Nos. 4,914,078 and 4,968,658. These layers are coated out of solution from presently
acceptable solvents such as methyl ethyl ketone. These types of coating solutions
were, however, not found to be useful on commercially available metallized (e.g.,
aluminized) polyester film. The most serious problem encountered in the use of these
specialized dye receptive coatings was that the coating would not strongly adhere
to the metallised surface. Even dye receptive coatings that were known to have good
adherent properties to metal were found to suffer from poor adhesion to the metallized
surface. It was discovered that the deposition of the vaporized metal onto the polymer
surface caused the underlying polymer on the surface to decompose, usually into dimers,
trimers and other lower molecular weight materials that would collect onto the surface
of the metallized layer. These materials would act much like a release surface and
greatly weaken the adherence of coatings applied thereto. Additionally, these materials
would not remove easily when treated by washing with ketones, alcohols, acetones,
tetrahydrofuran, or toluene. In fact, some of these solvents were not able to easily
penetrate the coating formed by the decomposition product of the polymer which deposited
itself on the surface of the vapor deposited metal.
[0006] Polyvinyl chloride derivatives and copolymers have been heavily used in thermal dye
transfer receptor sheets as receptor layers, because of their properties in these
areas. For example, U.S. Patent 4,853,365 discloses that chlorinated polyvinyl chloride,
used as a dye receptor, has good dye solubility and high dye receptivity. Similarly,
vinyl chloride/ vinyl acetate copolymers have also been used as receptor layers in
thermal dye transfer receptor sheets as described in Japanese published application
nos. 29,391 (1990) and 39,995 (1990). Japanese published application no. 160,681 (1989)
discloses dye acceptance layers comprising polyvinyl chloride-polyvinyl alcohol copolymers,
and Japanese published application nos. 43,092 (1990), 95,891 (1990) and 108,591 (1990)
discloses dye image receiving layers comprising a hydroxy modified polyvinyl chloride
resin and an isocyanate compound. U.S. Patent No. 4,897,377 discloses a thermal transfer
printing receiver sheet comprising a supporting substrate coated on at least one surface
with an amorphous polyester resin. Published European patent application 133,012 (1985)
discloses a heat transferable sheet having a substrate and a image-receiving layer
thereon comprising a resin having an ester, urethane, amide, urea, or highly polar
linkage, and a dye-releasing agent, such as a silicone oil, being present either in
the image-receiving layer or as a release layer on at least part of the image receiving
layer. Published European patent application 133,011 (1985) discloses a heat transferable
sheet based on imaging layer materials comprising first and second regions respectively
comprising (a) a synthetic resin having a glass transition temperature of from -100°
to 20°C, and having a polar group, and (b) a synthetic resin having a glass transition
temperature of 40°C or above.
[0007] U.S. Patent No. 4,968,658 teaches the use of a thermal transfer receptor surface
with a receiver coating comprising a dye-receptive material, a dye-permeable release
agent, and an alkoxylated Bisphenol A unsaturated polyester. Fumaric acid may also
be used in the layer.
[0008] Japan Patent Abstract No. 2025390 describes an image-receiving material for thermal
transfer capable of exhibiting favorably a metallic image with a metallic luster by
providing a metallic layer comprising a metallic powder dispersed therein, between
a dyeable resin layer and a base.
SUMMARY OF THE INVENTION
[0009] It is a aspect of the invention to provide a thermal dye or mass transfer receptor
element in intimate contact with a dye or thermal mass transfer donor sheet, the receptor
comprising a supporting substrate having on at least one surface thereof a dye or
thermal mass transfer receptive receiving layer comprising a polymeric substrate having
a vapor-deposited metal layer on at least one surface thereof. Coated on at least
one of the surfaces having a vapor-deposited metal layer thereon is a primer layer
coating comprising: a) a linear saturated thermoplastic polyester, and b) an alkyd
thermoset polyester resin. The thermoset resin is preferably cured with a melamine
crosslinking agent and/or a
para-toluene sulfonic acid. The receptor sheet comprises the described metallized polymer
substrate with the primer layer of the present invention thereon and a dye or thermal
mass transfer receptor layer coated on the primer. The dye or thermal mass transfer
receptive receiving layer is positioned in intimate contact with a dye or thermal
mass transfer donor layer during the thermal transfer process.
[0010] It is another aspect of this invention to provide thermal transfer receptor sheets
as described above wherein a polysiloxane release layer is coated on the dye or thermal
mass transfer receptive receiving layer or a release agent is incorporated into the
dye receptor layer.
[0011] The thermal transfer receptor sheets of the invention have good dye and mass transfer
receptivity and excellent dye-image thermal stability properties, and can provide
an accurate proofing image which resembles a printed image on a metal surface.
DETAILED DESCRIPTION OF THE INVENTION
[0012] The thermal dye and mass transfer receptor sheets used in the invention comprise
a supporting organic polymeric substrate having a vapor deposited metal layer, a primer
layer comprising a mixture of a linear, saturated thermoplastic polyester adhesive
and a thermoset (e.g., cured or crosslinked) polyester alkyd resin, and over said
primer layer, a dye receptive layer. The receptive layer is optionally coated with
a polysiloxane release layer or may contain release agents therein. The linear, saturated
polyester thermoplastic adhesive and polyester alkyd resin can be incorporated within
the receiving layer and further contain a crosslinking agent such as a isocyanate.
[0013] The dye or mass transfer image receptor layer used in the present invention must
be compatible as a coating with a number of resins for mass transfer and a number
of dyes for thermal dye transfer. Since different dye transfer media manufacturers
generally use different dye formulations in their donor sheets, the dye receiving
layer should have an affinity for several different dyes. Because the transfer of
dye from the dye donor sheet to the dye receptor sheet is essentially a contact process,
it is important that there be intimate contact (e.g., no air gaps or folds) between
the dye donor sheet and the dye receptor sheet at the instant of heating to effect
imaging. Many different dye receptor layer compositions are known in the art and they
are generally selected from polymer classes and mixtures thereof such as poly(vinyl
chloride), chlorinated poly(vinyl chloride), vinyl acetate/vinyl chloride copolymers,
silicone surfaces on polymeric bases, poly(methyl acrylate), polyvinyl acetals (e.g.,
polyvinyl butyral) and the like, which are preferred classes of polymers for receptor
layers. Surface modifying agents and treatments to alter opacity, smoothness, adhesion
of subsequent coatings, tint, and dye absorption are also conventionally used. When
used as a dye receptive layer, poly(vinyl chloride) is often used with an additional
resin, and usually additional or special plasticizers. Examples of such combinations
may be found generally in the art and, for example, in EPO 227 091, EPO 228 066, EPO
133011, EPO 133012, and EPO 228 065. Since poly(vinyl chloride) is a rigid resin,
the purpose of many of these additives is to plasticize the polymer.
[0014] Chlorinated poly(vinyl chloride) (CPVC) is a homopolymer of poly(vinyl chloride)
that has been subjected to a chlorination reaction. CPVC has may of the good dye receptive
properties of poly(vinyl chloride) and retains them at higher temperatures than PVC.
[0015] U.S. Patents 4,990,485; 4,931,423; 4,927,666; 4,914,078; and 4,910,189 show receptor
media which have compositions and constructions which could be used in combination
with the layers of the present invention.
[0016] The proper selection of softening temperature (e.g. glass transition temperature,
Tg) of the dye receiving layer is important in the preparation of the thermal dye
transfer receptor sheet. Preferably the dye receiving layer for thermal dye transfer
imaging should at least allow or enable increased solubilization of the dye, dye migration,
dye permeation, and/or surface release of the dye between the donor and receptor surfaces
below the temperatures employed to transfer dye from the dye donor sheet. The softening
point, however, must not allow the resin to become distorted, stretched, wrinkled,
etc. For use with thermal mass transfer imaging, the mass transfer receptor layer
should be readily bonded to by mass transfer resins, and the resins with the pigments
therein. In addition, the dye receptor sheet is preferably non-tacky and capable of
being fed reliably into a thermal printer, and is of sufficient durability that it
will remain useful after handling, feeding, and removal from imaging.
[0017] The dye or mass transfer receptor sheet used in the present invention may be prepared
by introducing the various components for making the receiving layer with suitable
solvents (e.g., tetrahydrofuran (THF), methyl ethyl ketone (MEK), toluene, and mixtures
thereof. The resulting solutions are mixed at room temperature (for example), then
the resulting mixture is coated onto the substrate and the resultant coating dried,
preferably at elevated temperatures. Suitable coating techniques include knife coating,
roll coating, curtain coating, spin coating, extrusion die coating, gravure coating,
etc. The receiving layer is preferably free of any observable colorant (e.g., an optical
density of less than 0.2, preferably less than 0.1 absorbance units). The thickness
of the receiving layer is from about 0.001 mm to about 0.1 mm, and preferably 0.005
mm to 0.010 mm.
[0018] Materials that have been found to be particularly useful for forming the receiving
layer include sulfonated hydroxy epoxy functional vinyl chloride copolymers as described
in U.S. Patent No. 4,910,189 and in another embodiment blends of sulfonated hydroxy
epoxy functional vinyl chloride copolymers with other polymers. Any of the well known
and/or commercially available materials known in the art as dye or thermal mass transfer
receptor polymeric compositions may be used in the practice of the present invention.
Polyvinyl resins, and especially polyvinyl chloride polymers and copolymers are widely
used in the art. Chlorinated polyvinyl chlorides and their blends have also found
wide acceptance. Other vinyl polymers and copolymers are also used in the art. Blends
of resins are often used to achieve a appropriate balance of properties in the receiving
layers of the art. The limiting factors to the resins chosen for the blend vary only
to the extent of compounding necessary to achieve the property desired. Preferred
blendable additives include, but are not limited to polyvinyl chloride, acrylonitrile,
styrene-acrylonitrile copolymers, polyesters (especially bisphenol A fumaric acid
polyester), acrylate and methacrylate polymers (especially polymethyl methacrylate),
epoxy resins, and polyvinyl pyrrolidone. When an additional polymer, copolymer, or
resin is used (as with an epoxidized, sulfonated polyvinyl chloride resin as in U.S.
4,910,189) the additional polymer is usually added in a amount of 75 percent by weight
or less of the resinous composition of the dye or thermal mass transfer receiving
layer, preferably in the amount of 25 to 75 percent by weight for non-release polymers,
or 0.01 to 15% for release polymers.
[0019] Release polymers are characterized by low surface energy and include silicone and
fluorinated polymers. Non-limiting examples of release polymers are poly dimethyl
siloxanes, perfluorinated polyethers, etc. Other conventional additives include, but
are not limited to, surfactants, plasticizers, UV stabilizers, coating aids, and the
like.
[0020] Suitable substrate materials may be any flexible material, optionally on which a
metal layer may be vapor depositied. Suitable substrates may be smooth (preferably)
or rough, transparent, opaque, and continuous or sheetlike. They may be porous or
essentially non-porous. Preferred backings are white-filled or transparent polyethylene
terephthalate or other temperature stable thermoplastic organic film forming polymers
(e.g., polycarbonates, polyolefins, etc.) Non-limiting examples of materials that
are suitable for use as a substrate include polyesters, especially polyethylene terephthalate,
polyethylene naphthalate, polysulfones, polystyrenes, polycarbonates, polyimides,
polyamides, cellulose esters, such as cellulose acetate and cellulose butyrate, polyvinyl
chlorides and derivatives, polyethylenes, polypropylenes, etc. The substrate generally
has a thickness of 0.02 to 1.5 mm, preferably 0.025 mm to 0.40 mm. If the substrate
is supported by a liner or other supporting backing, then the preferred range for
the substrate alone would be 0.0006 to 0.8 mm. The receptor substrate may be porous
or non-porous, and individual layers of the receptor or donor sheet may be porous
or non-porous so as to adjust thermal properties in the sheets and the transfer process.
[0021] By "non-porous" in the description of the invention it is meant that ink, paints
or other liquid coloring media will not readily flow through the substrate (e.g.,
less than 0.05 ml per second at 7 torr applied vacuum, preferably less than 0.02 ml
per second at 7 torr applied vacuum). The lack of significant porosity prevents absorption
of the heated receptor layer into the substrate. However, porosity has also been found
to be beneficial in localizing thermal events to the region of dye transfer and thereby
increasing transfer efficiency and quality.
[0022] The substrates used in the present invention may also have a supporting backing to
help in transporting the media through the printer and the imaging device. This is
essentially a non-critical, additional and optional structural feature. Such backings
may be directly or adhesively adhered to the substrate.
[0023] The metals which may be used as the vapor deposited material may be essentially any
metal which is capable of being vapor deposited. In practice, aluminum is the most
clearly preferred material, but other metals such as tin, steel, iron, copper, brass,
bronze, silver, gold, titanium, and the like may also have specialty applications.
The metals may be coated with dyes, as part of the metal layer or as a separate layer(s)
to improve tone, tint, or other visual aspects of coloration.
[0024] The thermal dye or mass transfer receptor layers used in the invention are used in
combination with a dye donor sheet wherein a dye image is transferred from the dye
donor sheet to the receptor sheet by the application of heat. The heat may be applied
by printheads, lasers, laser diodes, focused radiation, and the like, as is understood
in the art. The finer the resolution of the applied heat, the finer the resolution
of the image, within reasonable limits. The dye donor layer is placed in contact with
the receiving layer of the receptor sheet and selectively heated according to a pattern
of information signals whereby the dyes (or in the case of thermal mass transfer,
the dyes or pigment in a binder) are transferred from the donor sheet to the receptor
sheet. A pattern is formed thereon in a shape and density according to the intensity
of heat applied to the donor sheet. The heating source may be an electrical resistive
element, a laser (preferably an infrared laser diode), a infrared flash, a heated
pen, or the like. The quality of the resulting image can be improved by readily adjusting
the size of the heat source that is used to supply the heat energy, the contact position
of the donor sheet and the receptor sheet, and the heat energy. The applied heat energy
is controlled to give light and dark gradation of the image and for the efficient
diffusion of the dye from the donor sheet to ensure continuous gradation of the image
as in a photograph. Mass transfer imaging would give more limited gradation, but providing
solid blocks (as in half tone imaging systems) for graphics, lettering borders, and
the like. Thus, by using in combination with a dye donor sheet, the dye receptor sheet
of the invention can be utilized in the print preparation of a photograph by printing,
facsimile, or magnetic recording systems wherein various printers of thermal printing
systems are used, or print preparation for a television picture, or cathode ray tube
picture by operation of a computer, or a graphic pattern or fixed image for suitable
means such as a Video camera, and in the production of progressive patterns from an
original by an electronic scanner that is used in photomechanical processes of printing.
[0025] Suitable thermal dye transfer donor sheets for use in the invention are well known
in the thermal imaging art. Some examples are described in U.S. Patent No. 4,853,365
which is hereby incorporated by reference.
[0026] Other additives and modifying agents that may be added to the dye or mass transfer
receiving layer include UV stabilizers, heat stabilizers, suitable plasticizers, surfactants,
release agents, antistatic agents, etc., used in the receptor sheet of the present
invention. Similarly, mass transfer receptor layers will contain additives that will
facilitate the bonding and transfer of the mass transfer donor materials onto the
receptor sheet.
[0027] In a preferred embodiment, the dye or mass transfer receiving layer of the invention
is overcoated with a release layer or may contain release ingredients therein. The
release layer must be permeable to the dyes used under normal transfer conditions
in order for dye to be transferred to the receiving layer. Release materials suitable
for this layer may be fluorinated polymers such as polytetrafluoroethylene, and vinylidene
fluoride/vinylidene chloride copolymers, and the like, as well as dialkylsiloxane
based polymers such as polydimethylsiloxane, modified organopolysiloxanes, polyvinyl
butyral/siloxane copolymers such as Dai-Allomer™ SP-711 (manufactured by Daicolor
Pope, Inc., Rock Hill, SC) and urea-polysiloxane polymers.
[0028] Alternatively, improved release properties may be achieved by addition of a silicone
or mineral oil to the receiving layer during formulation.
[0029] As previously noted, the primer layer compositions used in the present invention
comprises a linear, saturated thermoplastic polyester and a thermoset alkyd polyester.
Many different types and classes of polymer solutions were evaluated before identifying
the primer compositions of the present invention as uniquely beneficial materials.
It is additionally important to one aspect of the present invention that the adhesive
could be coated out of ketone solutions (e.g., methyl ethyl ketone, methyl isobutyl
ketone, etc.). This provides the element with a highly compatible solvent system which
does not adversely affect other layers in the receptor element.
[0030] The preferred linear, saturated thermoplastic polyester adhesive present in the dye
receiving element used in the present invention is a polyethylene terephthalate adhesive
having a molecular weight in the range of 10,000 to 40,000, preferably 15,000 to 30,000.
Such polyesters are available from Bostik Chemical group, Emhart Corporation (e.g.,
Bostik 7695, 7651, 7614, and 7660) or from Goodyear Corp. (Vitel 3200, 3300, and 3550).
These commercial Bostik adhesives are available in toluene/MEK solvent solutions or
MEK solutions, with viscosities ranging from 1.2 - 1.5 Pa.s (1200-1500 cps) for 7695
to 0.11 - 0.16 Pa.s (110-160 cps) for 7614. The Vitel resins are solids. An alkyd
polyester is used in combination with the thermoplastic polyester, and the alkyd polyester
is crosslinked, as with a melamine crosslinking agent. Such materials are also individually
available (e.g., HKR 180®, HydroKinetics Corp.) The alkyd polyester may be further
crosslinked with materials such as para-toluene sulfonic acid and its salts.
[0031] A primer layer consisting of only the HKR 180 resin and para-toluene sulfonic acid
as a crosslinker provided adequate adhesion for a vapor coated film initially. However,
after the metal layer was overcoated with a thermal dye receiving layer, very poor
adhesion was observed for both layers.
[0032] When the linear polyester adhesive (e.g., Bostik 7695) was coated by itself as a
primer layer, it provided both good initial adhesion and good adhesion after application
of a dye receptor layer. However, the linear polyester was too tacky and caused blocking
of the coated film before application of the receptor layer. This made the intermediate
difficult to work with, because it is desirable to coat the layers separately and
then dry them after each coating.
EXAMPLES
[0033] The term "PVC" refers to polyvinyl chloride.
[0034] The term "PET" refers to polyethylene terephthalate.
[0035] The term "Meyer bar" refers to a wire wound rod such as that sold by R & D Specialties,
Webster, NY.
[0037] Butyl Magenta may be prepared as described in U.S. Patent 4,977,134 (Smith et al.);
HSR-31 was purchased from Mitsubishi Kasel Corp., Tokyo, Japan; AQ-1 was purchased
from Alfred Bader Chemical (Aldrich Chemical Co., Milwaukee, WI); Foron Brilliant
Blue was obtained from Sandoz Chemicals, Charlotte, NC; Heptyl Cyan and Octyl Cyan
were prepared according to the procedures described in Japanese published application
60-172,591.
[0038] A preferred example of a thermal receptor material is a 10% solvent mixture of VYNS-3®
(a vinyl chloride/vinyl acetate copolymer available from Union Carbide) and a multi-functionalized
polyvinyl chloride ( MR-120® available from Nippon Zeon). These two polymers are made
into solutions with methyl ethyl ketone at a 12/1 ratio of VYNS-3® to MR-120®. After
thoroughly mixing this solution, 0.7% by weight (total solids) of Vitel PE 2200® (a
copolyester resin made by Goodyear) and 1.5% by weight solids of Cyastat LS® (a quaternary
ammonium 3-lauramidopropyl triamethylammonium methylsulfate compound)were added. Prior
to coating, KF 393® (a modified organopolysiloxane made by Shin-Etsu Chemical Co.)
was added at a 0.07 to 1 ratio (with respect to the MR-120®), which can be applied
from solution. This solution was knife coated onto 0.05 mm (2 mil) PET film which
has been coated with vapor-deposited aluminum and the primer composition of the present
invention, the thermal receptor coating being applied at a 0.025 mm (1 mil) wet film
thickness. This was a coating of about 24.75 mg/m
2 (275 mg/square foot) dry coating weight.
[0039] A donor sheet was used to transfer the dye to the receptor using a thermal printer.
One useful printer used in the practice of the present invention was a Kyocera raised
glare thin film thermal print head (Kyocera Corp., Kyoto, Japan) with 8 dots per mm
and 0.3 watts per dot. In normal imaging, the electrical energy varies from 0 to 16
joules/cm
2, which corresponds to head voltages from 0 to 14 volts with a 23 ms burn time. In
all examples, the 3M Rainbow™ DeskTop Color Proofing system with 3M supplied donor
ribbon was used.
Components used:
[0040]
- VYNS - 3®
- -Vinyl chloride - vinyl acetate copolymer from Union Carbide
- MR 120®
- -Vinyl chloride copolymer from Nippon Zion Co. Ltd.
- KF 393®
- -Modified orgaopolysiloxane from Shin-Etsu
- Bostik 7695®
- -Polyester adhesive, toluene/MEK solvent. 6.5°C (17°F) flash point, viscosity of 1.2
- 1.5 Pa·s (1200-1500 cps). Intrinsic viscosity of 0.9 - 1.0 mm2/s (0.9 - 1.0 centistokes). Glass transition temperature -18° C.
[0041] The key features required of polyester additives within this invention were identified
by studying a series of thermoplastic copolyesters having both aromatic and aliphatic
groups. We also looked at resins with only aromatic groups and resins with only aliphatic
groups and just aliphatic polymers.
[0042] We have found that the oligomers present on the surface of the vapor-deposited film
can not be washed off or readily penetrated by common solvents such as ketones, alcohols,
acetones, tetrahydrofuran, or toluene. These oligomers, however, have been removed
with the use of chlorinated solvents such as 1,2-dichloroethane. Since the use of
chlorinated solvents is usually considered to be hazardous, the option of washing
aluminum coated polyester is impractical.
[0043] Many different primers were tried in an effort to apply receptor coatings to the
metallized surface of the polymers. Materials which are well known in the art as primers
between metals and polymers were tried, and even polymers used with methylene chloride
solvents could not penetrate the deposited detritus from the vapor deposition process.
This failure prevented the formation of a effective bond between the receptor coating
material and the metal. Amongst the materials tried according to the procedures of
the present invention described above in the example were linear, saturated thermoplastic
polyester (without additional additives), Vitel PE2200® polyester resin in MEK, Piccolastic
D125® styrene resin (a solvent-soluble stryene resin), styrene/acrylonitrile, polyvinyl
butyral, polycarbodiimide in methylene chloride and toluene, polyvinyl chloride in
tetrahydrofuran, chlorinated poly(vinyl chloride), water soluble acrylic latex (in
water), isooctyl acrylate/acrylic acid copolymer in acetone and heptane, octadecyl
acrylate/methyl acrylate/acrylic acid copolymer in ethanol and toluene, and a styrene/butadiene
elastomer in methyl ethyl ketone solution. These materials would suffer from such
various defects as weak adhesion and, particularly in the case of the linear polyester,
tackiness that rendered the material difficult to work with when applying further
coatings.
[0044] The key features that the polyester additive must contribute to the dye receptive
composition, comprising at least 50 percent polyvinyl chloride, Chlorinated polyvinyl
chloride, or polyvinyl chloride/polyvinyl acetate copolymers, include:
1. Acceptable mass transfer.
2. Acceptable dye transfer.
3. Acceptable dye transfer image density (four color black > 2.0 ROD density units).
4. Adhesion to numerous metal surfaces.
5. Acceptable dye image stability to heat and light exposure.
6. Aceptable shelf life stability of the receptor surface prior to and after imaging.
7. Non blocking/no tack.
8. Film former/smooth, uniform coating in order to provide intimate contact with donor
ribbon.
[0045] The polymers containing only aliphatic groups were polyester plasticizers such as
Paraplex H-25® from Rohm and Haas (a sebacic acid polyester), Paraplex H-50® (an adipic
acid polyester) and Plastolein 9750® from Emery Industries (an azalaic acid polyester).
All aliphatic polyesters in this study failed to perform adequately in the dye receptor
surface because of their inability to provide a adequate mass transfer surface due
to the plasticizer's lower glass transition temperature, which produced a oily/liquid
film surface. The aliphatic polyester plasticizers were generally mobile in the coated
film ad hindered dye stability and dye transfer uniformity. Due also to the characteristics
of aliphatic polyester resins, poor adhesion to metallic substrates was observed.
[0046] The polyester polymers derived from aromatic groups such as those found in thermoplastic
polyester films (e.g., Vitel 2200®) fail to perform adequately as the dye receptor
surface because of their low acceptance of dye image density and usually poorer dye
stability to heat and light. Other aromatic derived resins similar to the Vitel 2200®
such as polybutylene terephthalate (PBT) and polyethylene terephthalate (PET) consist
of the following components respectively, (PBT) = terephthalic acid and 1,4 butanediol
(PET) = terephthalic acid and ethylene glycol, showed similar problems.
[0047] Aromatic resins, aliphatic resins, and the aromatic/aliphatic copolyester resin blends
are all compatible with dye receptive vinyl chloride/vinyl acetate copolymer formulations.
Results indicate that aliphatic aromatic copolyester resin blends (as mixtures of
aliphatic and aromatic polymers and/or copolymers of aromatic and aliphatic monomeric
units) impart better adhesion to metallic surfaces without detrimental side effects
to the dye receptivity and stability. Generally the polyester resin should contain
5-95% by weight of aliphatic plus aromatic groups. The combination of aliphatic and
aromatic groups in the polyester resin provides the unique properties of hardness
and flexibility necessary for the thermal receptive film to function properly while
maintaining adequate adhesion. Polyester resins like Vitel 2200® are too hard (high
tensile strength and low elongation) and are unable to wet solvent insensitive substrates
(metallic film). While aliphatic polyesters, like Plastolein 9750® have excellent
wetting properties, they are too soft (low tensile strrength and elongation) which
inhibits adhesion.
[0048] The following materials are examples of copolyesters with aromatic and aliphatic
functional groups used in this evaluation. Vitel 2200®, which contains only aromatic
groups is included as a reference material (see the table below).
Raw Materials |
Type |
Bostik 7695 |
Bostik 7660 |
Bostik 7651 |
Bostik 7614 |
Vitel 2200 |
Vitel 3200 |
Vitel 3300 |
Vitel 3550 |
Vitel 3800 |
Terephthalic Acid |
A 1,4 |
24% |
14% |
|
|
25% |
33% |
24% |
15% |
|
Isophthalic Acid |
A 1,3 |
|
20% |
|
|
24% |
|
9% |
10% |
|
|
|
|
|
|
|
|
|
|
|
|
Adipic Acid |
C4 |
17% |
7% |
|
|
|
|
|
|
|
Sebacic Acid |
C8 |
7% |
7% |
|
|
|
15% |
|
|
|
Azelaic Acid |
C7 |
|
|
|
|
|
|
15% |
24% |
|
|
|
|
|
|
|
|
|
|
|
|
1,6 Hexanediol |
S |
15% |
7% |
|
|
|
|
|
|
|
1,4 Butanediol |
S |
|
42% |
|
|
|
|
|
|
|
Ethylene Glycol |
S |
36% |
|
|
|
26% |
32% |
31% |
51% |
|
Neopentyl Glycol |
B |
|
|
|
|
24% |
20% |
20% |
|
|
|
|
|
|
|
|
|
|
|
|
|
Tg °C |
|
-18 |
-15 |
20 |
56 |
63 |
12 |
11 |
-15 |
-33 |
|
|
|
|
|
|
|
|
|
|
|
A-Aromatic |
|
|
|
|
|
|
|
|
|
|
S-Strait |
|
|
|
|
|
|
|
|
|
|
B-Branched |
|
|
|
|
|
|
|
|
|
|
[0049] Vitel 3800® has a higher aliphatic to aromatic ratio than the other Vitel resins
shown in the table. Bostik 7651 and Bostik 7614 have a higher aromatic to aliphatic
ratio than do the other Bostik resins.
[0050] All solutions were coated with a #32 Meyer bar, hot air gun dried and then placed
into a 87.4°C (230° F) dry oven for 4 minutes. Coatings were done on 0.05 mm (2 mil).
aluminum vapor coated polyester film (Al-PET). All samples were imaged using the 3M
Rainbow™ model 2710 Desk Top Color Proofing System. All density readings were taken
with a Gretag SPM 100 densitometer.
Standard solution:
[0051]
Resin |
Amount in grams |
VYNS-3 (10% solids in MEK) |
24.0 |
MR120 (10% solids in MEK) |
2.0 |
Cyastat LS (10% solids in MEK) |
0.43 |
KF393 (1.0% solids in MEK) |
1.4 |
[0052] To the standard solution above the following copolyester/polyester resins were added:
1. Bostik 7695® (12% solids in MEK) 14.2 grams
2. Vitel 3550® (10% solids in MEK) 17.0 grams
3. Vitel 3200® (10% solids in MEK) 17.0 grams
4. Vitel 3300® (10% solids in MEK) 17.0 grams
5. Vital 3800® (10% solids in MEK) 17.0 grams
6. Vital 2200® (10% solids in MEK) 17.0 grams
7. No other additives -- standard solution only
8. Vitel 3550® alone -- no standard solution
9. Vitel 3800® alone -- no standard solution
10. Bostik 7695® alone -- no standard solution
Results:
[0053]
Sample |
Base |
Yellow |
Magenta |
Cyan |
Black(4 color) |
1 |
Al-PET |
1.23 |
1.00 |
0.91 |
1.50 |
2 |
Al-PET |
1.30 |
0.94 |
1.07 |
1.60 |
3 |
Al-PET |
1.12 |
0.98 |
0.99 |
1.47 |
4 |
Al-Pet |
1.21 |
0.93 |
1.00 |
1.36 |
5 |
Al-PET |
1.45 |
1.00 |
1.90 |
----- |
6 |
Al-PET |
Not tested due to the low imaging densities |
7 |
Al-PET Clear PET |
1.27 |
0.95 |
0.93 |
1.60 |
8 |
Al-PET |
Surface was too tacky to run through the printer and image. |
9 |
Al-PET |
Surface was too tacky to run through the printer and image. |
10 |
Al-PET |
Surface was too tacky to run through the printer and image. |
[0054] The adhesion was good in samples 1, 3, and 4, very good in sample 2, fair to poor
in example 5, and very poor in samples 6 and 7.
[0055] It can be concluded that polyester resins containing both aromatic and aliphatic
groups provide the receptive layers of the present invention with improved adhesion
to metal surfaces, uninhibited mass transfer and dye receptivity, minimal, negative,
effects on dye image stability to heat and light, and good film forming characteristics.
[0056] As mentioned previously, the linear, saturated thermoplastic polyester adhesive can
be incorporated within the dye or mass transfer receiving layer and additionally contain
crosslinking agents such as isocyanates. This alternative embodiment does not require
a prime layer and can be coated directly onto a metallized base without damaging the
adhesion between the layers. Such a composition may have a formulation such as the
following, which has been found to be effective in this practice:
- 14.2 grams
- Bostik 7695® (12% solids in MEK)
- 3.4 grams
- Boscodur 21® (1% solids in MEK)
- 2.0 grams
- MR-120® (10% solids in MEK)
- 24 grams
- VYNS-3® (10% solids in MEK)
- 1.4 grams
- KF393® (1% solids in MEK)
- 0.43 grams
- Cyastat LS® (10% solids in isopropanol/MEK)
Boscodur 21® is a 4',4'-diphenylmethane diisocyanate, solvent based curing agent
from Bostik, Inc.
1. System für den thermischen Transfer, umfassend ein Donorelement für den thermischen
Transfer in Berührung mit einem Empfängerelement für den thermischen Transfer, wobei
das Empfängerelement für den thermischen Farbstofftransfer ein Substrat umfaßt, das
eine aus der Dampfphase abgeschiedene Metallschicht, eine Grundierschicht auf der
Metallschicht, wobei die Grundierschicht dadurch gekennzeichnet ist, daß sie einen
thermoplastischen, linearen, gesättigten Polyester mit aliphatischen und aromatischen
Gruppen und einen wärmegehärteten Alkydpolyester umfaßt, und auf der Grundierschicht
eine Empfängerschicht aufweist, wobei die Empfängerschicht in Kontakt mit dem Donorelement
für den thermischen Transfer ist.
2. System nach Anspruch 1, wobei die Empfängerschicht eine Empfängerschicht für den thermischen
Farbstoff-Transfer ist und ein Vinylchlorid-Copolymer mit einer Glasübergangstemperatur
der Zusammensetzung zwischen 50 und 85 °C, einem Massenmittel der Molmasse zwischen
10 000 und 100 000 g/mol, einem Hydroxyl-Äquivalenzgewicht zwischen 1000 und 7000
g/mol, einem Sulfonat-Äquivalenzgewicht zwischen 5000 und 40 000 g/mol und einem Epoxy-Äquivalenzgewicht
zwischen 500 und 7000 g/mol umfaßt.
3. System für den thermischen Transfer nach Anspruch 1, wobei die Empfängerschicht eine
Empfängerschicht für den thermischen Farbstoff-Transfer ist, wobei eine Polysiloxan-Trennschicht
auf die oder in der Empfängerschicht aufgetragen ist.
4. System für den thermischen Transfer nach Anspruch 1, wobei die thermische Donorfolie
ein Substrat umfaßt, das nur auf einer seiner Oberflächen eine Schicht aufweist, die
einen thermisch übertragbaren Farbstoff umfaßt.
5. Verfahren zur Übertragung eines Bildes unter Verwendung des Systems des thermischen
Transfers nach Anspruch 1, wobei Wärme in einer bildweisen Verteilung auf die Seite
der thermischen Donorfolie einwirken gelassen wird, die sich am weitesten entfernt
von dem Empfängerelement befindet, wobei die Wärme in einem Umfang einwirken gelassen
wird, der ausreichend ist, um Material thermisch von dem Donorelement zu übertragen.
6. System für den thermischen Farbstoff-Transfer, umfassend ein Empfängerelement für
den thermischen Transfer im innigen Kontakt mit einer Folie für den thermischen Transfer,
wobei das Empfängerelement ein Substrat umfaßt, bei dem sich auf wenigstens einer
seiner Oberflächen in Kontakt mit der Folie für den thermischen Transfer eine aus
der Dampfphase abgeschiedene Metallschicht befindet, wobei sich eine Grundierschicht
auf der Metallschicht befindet und sich auf der Grundierschicht eine Schicht für den
thermischen Massentransfer oder für die Farbstoffaufnahme befindet, wobei die Grundierschicht
dadurch gekennzeichnet ist, daß sie einen linearen, gesättigten, thermoplastischen
Polyester mit aliphatischen und aromatischen Gruppen und ein wärmegehärtetes Alkydpolyester-Harz
umfaßt.
7. System nach Anspruch 6, wobei die Aufnahmeschicht eine thermischen Farbstoff aufnehmende
Schicht ist, die ein Vinylchlorid-Copolymer mit einer Glasübergangstemperatur der
Zusammensetzung zwischen 55 und 70 °C, einem Massenmittel der Molmasse zwischen 20
000 und 60 000 g/mol, einem Hydroxyl-Äquivalenzgewicht zwischen 1500 und 4000 g/mol,
einem Sulfonat-Äquivalenzgewicht zwischen 9000 und 23 000 g/mol und einem Epoxy-Äquivalenzgewicht
zwischen 500 und 7000 g/mol umfaßt.
1. Système de transfert thermique comprenant un élément donneur de transfert thermique
en contact avec un élément récepteur de transfert thermique, ledit élément récepteur
de transfert thermique pour couleur comprenant un substrat ayant une couche métallique
déposée par vapeur, une couche primaire sur ladite couche métallique, dans lequel
ladite couche primaire est caractérisée en ce qu'elle comprend un polyester thermoplastique
saturé de manière linéaire, ayant des groupes aliphatiques et aromatiques et un polyester
alkyde thermodurcissable, et au-dessus de ladite couche primaire une couche réceptrice,
ladite couche réceptrice étant en contact avec ledit élément donneur de transfert
thermique.
2. Système selon la revendication 1, dans lequel ladite couche réceptrice est une couche
réceptrice de transfert thermique pour couleur, et comprend un copolymère de chlorure
de vinyle ayant une température de transition vitreuse de composition située entre
50 et 85°C, un poids moyen en poids moléculaire compris entre 10 000 et 100 000 g/mole,
un poids équivalent en hydroxyle compris entre 1000 et 7000 g/mole, un poids équivalent
en sulfonate entre 5000 et 40 000 g/mole, et un poids équivalent en époxy entre 500
et 7000 g/mole.
3. Système de transfert thermique selon la revendication 1, dans lequel ladite couche
réceptrice est une couche réceptrice de transfert thermique pour couleur avec une
couche libérant du polysiloxane couvrant la surface ou à l'intérieur de ladite couche
réceptrice.
4. Système de transfert thermique selon la revendication 1, dans lequel ladite feuille
donneuse thermique comprend un substrat ayant sur une seule face de celui-ci une couche
comprenant une teinture pouvant être transférée de manière thermique.
5. Procédé de transfert d'une image en utilisant le système de transfert thermique selon
la revendication 1, dans lequel de la chaleur est appliquée selon une distribution
à la manière d'une image, sur un côté de ladite feuille donneuse thermique, le plus
loin possible de ladite couche réceptrice, ladite chaleur étant appliquée en une quantité
suffisante pour transférer de manière thermique de la matière depuis ledit élément
donneur.
6. Système de transfert thermique de couleur comprenant un élément récepteur de transfert
thermique en contact étroit avec une feuille donneuse thermique, ledit élément récepteur
comprenant un substrat ayant, sur au moins une surface de celui-ci au contact avec
ladite feuille donneuse de transfert, une couche métallique déposée par vapeur, une
couche primaire située sur ladite couche métallique et, par-dessus ladite couche primaire,
une couche thermique de transfert de matière ou réceptrice de couleur, dans lequel
ladite couche primaire est caractérisée en ce qu'elle comprend un polyester thermoplastique
saturé de manière linéaire, ayant des groupes aliphatiques et aromatiques et une résine
alkyde polyester thermodurcissable.
7. Système selon la revendication 6, dans lequel ladite couche réceptrice est une couche
réceptrice thermique pour couleur qui comprend un copolymère de chlorure de vinyle
ayant une température de transition vitreuse de composition comprise entre 55 et 70°C,
un poids moyen en poids moléculaire comprise entre 20 000 et 60 000 g/mole, un poids
équivalent hydroxyle compris entre 1500 et 4000 g/mole, un poids équivalent sulfonate
compris entre 9000 et 23 000 g/mole, et un poids équivalent époxy entre 500 et 7000
g/mole.