[0001] This invention relates to dye-receiving elements used in thermal dye transfer, and
more particularly to the use of a particular stabilizer for such elements.
[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. Further details of this
process and an apparatus for carrying it out are contained in U.S. Patent 4,621,271.
[0003] Dye-receiving elements for thermal dye transfer generally comprise a polymeric dye
image-receiving layer coated on a support. A compression, or cushion intermediate
layer, for example as taught in U.S. Patent 4,734,397 may also be present between
the support and the dye image-receiving layer. Such cushion layers promote better
contact between a dye-donor element and the dye-receiving element, which minimizes
the formation of image defects during dye transfer and improves the scratch resistance
of the dye-receiving element. In addition, subbing layers, for example as taught by
U.S. Patent 4,748,150, may also be present between the various layers to promote adhesion.
[0004] U.S. Patent 4,965,241 relates to the use of amino-functionalized silane coupling
agents as subbing layers in thermal dye transfer receivers. However, there is a problem
with these subbing layers in that both the dark-keep thermal stability and the fingerprint
resistance of the dyes in the receiver element are negatively affected.
[0005] U.S. Patent No. 4,705,521 relates to improving the light stability of transferred
dyes in a receiver element by providing a stabilizer in the dye-receiving layer and
reheating the receiver after thermal dye transfer. However, there is a problem with
this process in that it involves a reheating step, which is an extra step in the thermal
dye transfer process.
[0006] It is an object of this invention to provide a dye-receiving element wherein the
dye-receiving layer will significantly enhance the dark-keep thermal stability of
imaged dyes in the dye-receiving layer when an amino-functionalized polymeric material
is used as a subbing layer between the support and the dye-receiving layer. It is
another object of this invention to provide a dye-receiving element wherein the fingerprint
resistance of imaged dyes in the dye-receiving layer is improved, when an amino-functionalized
polymeric material is used as a subbing layer between the support and the dye-receiving
layer.
[0007] These and other objects are achieved in accordance with this invention which comprises
a dye-receiving element for thermal dye transfer comprising a a support having on
one side thereof, in order, a subbing layer of an amino-functionalized polymer, and
a polymeric dye image-receiving layer, the receiving layer containing a stabilizer
having the following structure:
- wherein
- n is an integer of 4 to 12, and
R is a substituted or unsubstituted alkyl group of at least 6 carbon atoms, such as
chlorooctyl, s-dodecyl, 3-hydroxyhexyl, cyclohexyl, hexyl, octyl, dodecyl, hexadecyl,
methoxyoctyl, 10-acetoxydecyl, 12-methoxycarbonyldodecyl, etc.
[0008] A substituted alkyl group in the above formula includes an alkyl group substituted
with one or more of the following groups: halogen, cyano, alkyl, aryl, hetaryl, nitro,
carboxy, alkoxy, aryloxy, alkoxycarbonyl, aryloxycarbonyl, acyloxy, aryloxy, acylamino,
arylsulfonamido, alkylsulfonamido, hydroxy, alkylcarbamoyl, dialkylcarbamoyl, arylcarbamoyl,
diarylcarbamoyl, arylalkylcarbamoyl, alkylureido, arylureido, alkylthio, arylthio,
etc.
[0009] In a preferred embodiment of the invention, R in the above formula is C
8H
17 and n is 8. In another preferred embodiment, R in the above formula is C
12H
25 and n is 8.
[0010] The stabilizer compounds of the invention may be employed at any concentration which
is effective for the intended purpose. In general, good results have been obtained
at a coverage of from about 0.05 to about 1 g/m
2.
[0011] Compounds included within the scope of this formula include the following:
Compound 1
[0012]

Compound 2
[0013]

Compound 3
[0014]

Compounds 4-8:
[0015]

Compound 4
[0016] n is 8 and R is C
10H
20O
2CCH
3
Compound 5
[0017] n is 12 and R is c-C
6H
11
Compound 6
[0018] n is 6 and R is C
12H
24CO
2CH
3
Compound 7
[0019] n is 10 and R is C
8H
16Cl
Compound 8
[0020] n is 4 and R is CH
2CH(OCH
3)C
6H
13
[0021] It has been found unexpectedly that incorporation of certain hindered-amine light
stabilizers, i.e., hindered aminoethers of the above formula, in the dye-receiving
layer will significantly enhance dark-keep thermal stability and will improve fingerprint
resistance of imaged dyes in the dye-receiving layer when amino-functionalized polymeric
materials are used as the subbing layer between the support and the dye-receiving
layer. The stabilizer compounds of this type may be prepared by the techniques described
in EPA 309402A-1 or J.Poly.Sci., Poly.Chem.Ed.,
23, 1477 (1985).
[0022] An amino-functionalized polymeric subbing layer having a silicon oxide backbone employed
in this invention is described in U.S. Patent 4,965,241.
[0023] The support for the dye-receiving element of the invention may be transparent or
reflective, and may comprise a polymeric, a synthetic paper, or a cellulosic paper
support, or laminates thereof. Examples of transparent supports include films of poly(ether
sulfone)s, polyimides, cellulose esters such as cellulose acetate, poly(vinyl alcohol-co-acetal)s,
and poly(ethylene terephthalate). The support may be employed at any desired thickness,
usually from about 10 mm to 1000 mm. Additional polymeric layers may be present between
the support and the dye image-receiving layer. For example, there may be employed
a polyolefin such as polyethylene or polypropylene. White pigments such as titanium
dioxide, zinc oxide, etc., may be added to the polymeric layer to provide reflectivity.
The receiver element may also include a backing layer such as those disclosed in U.S.
Patents 5,011,814 and 5,096,875.
[0024] In a preferred embodiment of the invention, a paper substrate support bearing a polypropylene
layer is used. In a further preferred embodiment, a microvoided composite film is
employed such as OPPalyte 350TW®, (Mobil Chemical Co.) as disclosed in U.S. Patent
No. 5,244,861. These polyolefin supports may be subject to a corona discharge treatment
prior to being coated with the subbing layer.
[0025] The dye image-receiving layer of the dye-receiving elements of the invention may
comprise, for example, a polycarbonate, a polyurethane, a polyester, poly(vinyl chloride),
poly(styrene-co-acrylonitrile), polycaprolactone or mixtures thereof. In a preferred
embodiment, polycarbonates are employed. The dye image-receiving layer may be present
in any amount which is effective for the intended purpose. In general, good results
have been obtained at from about 1 to about 10 g/m
2. An overcoat layer may be further coated over the dye-receiving layer such as those
described in U.S. Patent 4,775,657.
[0026] Conventional dye-donor elements may be used with the dye-receiving element of the
invention. Such donor elements generally comprise a support having thereon a dye-containing
layer. Any dye can be used in the dye-donor employed in the invention provided it
is transferable to the dye-receiving layer by the action of heat. Especially good
results have been obtained with diffusible dyes. Dye donors applicable for use in
the present invention are described, e.g., in U.S. Patents 4,916,112, 4,927,803 and
5,023,228.
[0027] The dye-donor element employed in certain embodiments of the invention may be used
in sheet form or in a continuous roll or ribbon. If a continuous roll or ribbon is
employed, it may have only one dye thereon, mixtures of dyes or may have alternating
areas of different dyes such as cyan, magenta, yellow, black, etc., as disclosed in
U.S. Patent 4,541,830.
[0028] A process of forming a dye transfer image according to the invention comprises:
a) imagewise-heating a dye-donor element comprising a support having thereon a dye
layer comprising a dye dispersed in a binder, and
b) transferring a dye image to a dye-receiving element as described above to form
said dye transfer image.
[0029] In a preferred embodiment of the invention, a dye-donor element is employed which
comprises a poly(ethylene terephthalate) support coated with sequential repeating
areas of cyan, magenta and yellow dye, and the dye transfer process steps are sequentially
performed for each color to obtain a three-color dye transfer image.
[0030] Thermal printing heads which can be used to transfer dye from dye-donor elements
to the receiving elements of the invention are available commercially. Alternatively,
other known sources of energy for thermal dye transfer, such as laser or ultrasound,
may be used.
[0031] A thermal dye transfer assemblage of the invention comprises a) a dye-donor element
as described above, and b) a dye-receiving element as described above, the dye-receiving
element being in a superposed relationship with the dye-donor element so that the
dye layer of the donor element is in contact with the dye image-receiving layer of
the receiving element.
[0032] When a three-color image is to be obtained, the above assemblage is formed on three
occasions during the time when heat is applied by the thermal printing head. After
the first dye is transferred, the elements are peeled apart. A second dye-donor element
(or another area of the donor element with a different dye area) is then brought into
register with the dye-receiving element and the process repeated. The third color
is obtained in the same manner.
[0033] The following Example is provided to illustrate the invention.
Example:
[0034] The materials referred to in this example are the following:
- Prosil® 221
- aminopropyl triethoxysilane (PCR, Inc.)
- Z-6020
- N-2-aminoethyl)-3-aminopropyl triethoxysilane (Dow-Corning Co.)
- Polymin P®
- polyethylenimine (BASF Corp.)
- MEK
- methyl ethyl ketone
- Makrolon®
- a polyether-modified bisphenol A
- KL3-1013
- polycarbonate block copolymer (Bayer Co.)
- Lexan® 141-112
- bisphenol A polycarbonate (General Electric Co.)
- Fluorad® FC-431
- a perfluorinated alkylsulfonamido alkylester surfactant (3M Corp.)
- DBP
- di-n-butyl phthalate
- DPP
- di-phenyl phthalate
Control Stabilizer A
[0035]

Control Stabilizer B
[0036]

Control Stabilizer C
[0037]

Control Stabilizer D
[0038]

[0039] Subbing layer coating solutions were prepared separately by dissolving the individual
amino-functional organosilanes, such as Prosil® 221 or Z-6020, in an ethanol-methanol-water
solvent mixture.
[0040] Subbing layer coating solutions with amino-functional materials, such as Polymin
P®, were prepared as 0.8% aqueous solutions.
[0041] The above test solutions were then coated onto a polypropylene-laminated paper support
with a TiO
2-pigmented polypropylene skin (OPPalyte® 350 TWK packaging film from Mobil Chemical
Co. laminated to paper support) (see U.S. Patent 5,244,861) at a dry coverage of 0.11
g/m
2. Prior to coating, the support was subjected to a corona discharge treatment at approximately
450 joules/m
2.
[0042] Each of the above test samples was overcoated with a dye-receiving layer comprising
Makrolon® KL3-1013 (1.82 g/m
2), GE Lexan® 141-112 (1.49 g/m
2), Fluorad® FC-431 (0.011 g/m
2), and a mixture of DBP, DPP and stabilizer when present (see Table), in a total coverage
of 0.66 g/m
2 coated from methylene chloride. Stabilizer levels were adjusted to give equimolar
amounts.
[0043] The dye-receiving layer was then overcoated at 0.22 g/m
2 with a solvent mixture of methylene chloride and trichloroethylene, a polycarbonate
random terpolymer with blocks of bisphenol A (50 mole-%), diethylene glycol (49 mole-%),
and polydimethylsiloxane (1 mole-%) (2500 MW).
[0044] Dye-donor elements were prepared and used for imaging the above test receivers as
described in detail in U.S. Patent No. 5,262,378, col. 6, line 42 through col. 8,
line 29.
[0045] The imaged receiver samples were then subjected to a dark-keep thermal stability
test at 60° C/70 % RH for three days. The Status A green reflection densities, before
and after keeping, of the magenta patch having an initial density of 1.7 were then
compared, and the density loss was calculated and listed in the Table.
[0046] A fingerprint test was performed by applying the fingerprint of a thumb covered with
Veriderm oil (Product 936Fu, no perfume, from Upjohn Co.) through a 1 cm
2 square cut out from polyethylene-coated paper stock, onto a 1.0 density (Status A)
neutral patch (obtained by superimposed images from the cyan, magenta, and yellow
donor patches printed onto imaged receiver samples as described above). These fingerprinted,
neutral patches were then subjected to 60°C and 70% RH storage for three days. The
Status A red, green, and blue reflection densities before and after keeping were then
compared, and the percent density loss was calculated. The Table shows sample identifications
and test results.

[0047] The above data show that use of the stabilizers of the invention in a thermal dye
transfer receiver element containing a polymeric amino-functionalized subbing layer
provides protection against dye losses during dark-keeping and resistance to fingerprint
damage.
1. A dye-receiving element for thermal dye transfer comprising a support having on one
side thereof, in order, a subbing layer of an amino-functionalized polymer, and a
polymeric dye image-receiving layer, said dye image-receiving layer containing a stabilizer
having the following structure:
wherein n is an integer of 4 to 12, and
R is a substituted or unsubstituted alkyl group of at least 6 carbon atoms.
2. The element of claim 1 wherein R is C8H17 and n is 8.
3. The element of Claim 1 wherein R is C12H25 and n is 8.
4. The element of Claim 1 wherein said polymeric dye image-receiving layer comprises
a polycarbonate.
5. The element of Claim 1 wherein said support is a polyolefin-coated paper support.
6. The element of Claim 1 wherein said stabilizer is present at a coverage of from 0.05
to 1 g/m2.
7. A process of forming a dye transfer image comprising:
a) imagewise-heating a dye-donor element comprising a support having thereon a dye
layer comprising a dye dispersed in a binder, and
b) transferring a dye image to a dye-receiving element to form said dye transfer image,
wherein said dye-receiving element comprises a support having on one side thereof,
in order, a subbing layer of an amino-functionalized polymer, and a polymeric dye
Image-receiving layer, said dye image-receiving layer containing a stabilizer having
the following structure:
wherein n is an integer of 4 to 12, and
R is a substituted or unsubstituted alkyl group of at least 6 carbon atoms.
8. The process of claim 7 wherein R is C8H17 or C12H25 and n is 8.
9. A thermal dye transfer assemblage comprising:
a) a dye-donor element comprising a support having thereon a dye layer comprising
a dye dispersed in a binder, and
b) dye-receiving element comprising a support having on one side thereof, in order,
a subbing layer of an amino-functionalized polymer, and a polymeric dye image-receiving
layer, said dye image-receiving layer containing a stabilizer having the following
structure:

wherein n is an integer of 4 to 12, and
R is a substituted or unsubstituted alkyl group of at least 6 carbon atoms.
10. The assemblage of claim 9 wherein R is C8H17 or C12H25 and n is 8.