[0001] This invention relates to film products for use in receiving images and subsequent
use in printing processes.
Background to the invention
[0002] Electrophotographic machines such as laser printers and photocopiers in which toner
is applied imagewise to a substrate by electrostatic attraction are ubiquitous. By
and large they are superb for making ordinary images. With some limitations they are
adequate for overhead transparencies and, in principle but not in practice, they should
make an excellent potential source of film positives and negatives for the printing
industry: e.g. in offset, screen and flexo printing.
[0003] Unfortunately, the charged nature of the toner particles used in electrophotographic
machines leads to a mutual repulsion and the image is not a solid area: there is often
a gap between each toner particle. This gap is usually not noticeable for ordinary
images: it reduces somewhat the contrast of overhead projections but, more seriously,
this gap lets through sufficient light to reduce the contrast of the positive or negative.
Hence the use of electrophotographic machines for film positives and negatives is
limited.
[0004] Electrophotographic systems usually incorporate a heat processing step to fuse the
toner particles to each other and to the substrate. Often this is a heated roller
system, though it can also be an intense burst of heat from a lamp. The fusing system
is a compromise. It needs to take place at sufficiently low temperatures to be energy
efficient, to allow substrate to pass through quickly and to minimize the distortion
of the substrate. To provide better fusing of the toner it is best to increase the
temperature and pressure within the fusing system of the electrophotographic machine.
This can however melt the toner and force it to flow together better. Although there
are many differences in machine design, the vast majority have opted for a lower temperature
that gives adequate print image results but insufficient coalescence of the toner
for producing film positives and negatives. Current commercially available laser imageable
films include "Delta Laserfilm" and "Folaproof Laser Film".
[0005] Another approach is to increase the amount of toner deposited. But this can often
have detrimental effects on image quality and consumables cost so it is not usually
a favoured option.
[0006] Yet another approach, when using the system for film positives or negatives, is to
mask the problem through the use of a translucent film. The scattering of the light
reduces the effective amount of light passed by the gaps between the toner particles
and increases the image contrast. However, this approach reduces resolution and provides
only a modest increase in contrast.
[0007] A further approach to the problem is to post-treat the image with solvent, sometimes
in combination with heat and/or pressure. This can achieve excellent results: the
toner particles fuse together and give a solid black image which can easily be used
as a printing positive or negative. However, this is an extra processing step, it
involves extra cost, it requires extra time to ensure that the solvent is fully evaporated
and the use of solvents can give rise to odour or health and safety issues.
[0008] US-A-4461823 (DuPont) describes a "prolonged tack toner" in a process to develop
a substrate containing a latent image. The "prolonged tack toner" is prepared from
a thermoplastic resin (e.g. polymethyl methacrylate/ methacrylic acid) and a solid
plasticiser (e.g. triphenyl phosphate). The mixture becomes tacky upon heating and
retains this tackiness for a considerable time after cooling. The "prolonged tack
toner" image can then be transferred to another substrate to give an image with an
increased optical density. EP-A-0501396 (DuPont) similarly uses a solid plasticiser
and monomer/photoinitiator mixture as a "prolonged tack toner".
[0009] GB-A-2085806 discloses a receiving substrate for use in a reflex thermoremanent magnetic
imaging method. The receiving substrates specifically disclosed are bond-like papers
which are treated during manufacture with a binder and plasticiser combination. The
substrate is used in pressure transfer thereto of a toner-developed latent magnetic
image produced by reflex thermoremanent magnetic imaging of a magnetic imaging member.
The binder and plasticiser treatment is shown to provide improved adhesive properties
with respect to toner transfer during pressure transfer.
[0010] WO-A-95/18992 describes a receptor layer comprising a blend of an acrylic resin,
a vinyl resin, a solution or dispersion grade rubber and a plasticiser. An image is
applied to the receptor layer by thermally bonding electrostatic toners which were
previously printed onto a transfer medium. The receptor layer is stated to be particularly
suitable for printing graphics on plasticised polyvinyl chloride coated fabric for
use on soft-sided vehicles where previous receptor layers did not withstand the flexing,
rolling, flapping and cold-flexing to which the fabric is subjected in use.
[0011] US-A-5665504 describes the creation of simulated, photographic-quality prints using
non-photographic imaging such as xerography and ink jet printing. This is achieved
by means of a coated backing sheet having successive first and second coating layers,
the first layer comprising an adhesive polymer for adhering the backing sheet to imaged
transparent substrates, whilst the second layer prevents premature activation of the
first layer and contains a plasticiser having at melting point of less than 75°C.
In use, an ink-jet or xerographic image is formed on a transparency which is then
laminated to the backing sheet by application of heat and pressure, in order to create
the simulated, photographic-quality prints.
[0012] US-A-5045426 discloses a coated cellulosic (and therefore opaque) web which is usable
for producing security documents, such as cheques, which are to be printed using non-contact
printing devices such as laser printers. The web is coated with a polymeric toner
adhesion-enhancing composition which may contain a plasticiser for the purpose of
enhancing the flexibility of the coating.
[0013] US-A-4526847 describes a transparency for the formation of an adherent electrostatic
image thereon. The transparency comprises a polyester base film with a nitrocellulose
coating layer which contains a plasticiser, preferably castor oil, which contributes
to the adherence of the coating layer to the base film and to the flexibility of the
coating layer.
[0014] US-A-4259425 describes an electrographic recording material comprising a conductive
sheet coated with an electrically insulating layer comprising up to 500 parts by weight
of a finely divided pigment per 100 parts by weight of polymeric binder comprising
a particular polyvinyl acetal, polystyrene or poly(α-methylstyrene) and a plasticising
liquid polystyrene. The coated material provides improved print retention when printed
on electrographically.
The invention
[0015] According to the present invention, there is provided a substrate for use in producing
film positives by means of an electrographic printing process, the substrate comprising:
a base layer, an optional adhesive layer and a film-coating layer, the film-coating
layer having within its bulk a toner-coalescing agent which, under the influence of
the heat of the fusing step of the electrographic printing process, has an effect
of improving the degree of coalescence of the toner applied to the surface of the
film-coating layer.
[0016] In this invention the benefits of the solvent approach without substantial drawbacks
can be achieved. In effect, the solvent is built into the toner-receptive coating
of the film. The invention also avoids the inclusion of a liquid solvent within this
coating - it would be unpleasant to handle, would leave deposits on the rollers of
the laser printer and would be subject to easy image wipe-off and smearing.
[0017] The invention uses a heat-activated toner-coalescing system. The bulk of the system
can be a polymer or polymer blend that could be used as an ordinary electrographic
system. For example, it can have adequate toner adhesion and does not contaminate
the printer mechanism. The bulk system would however suffer from the defects listed
above. Within the bulk system a chemical blend is provided which, at ambient temperatures,
imparts no special properties to the bulk. However, using the heat provided during
the fusing stage (and, optionally, in a further heat processing step), the chemical
blend is able to migrate to the surface of the system and has sufficient chemical
compatibility with the toner (when hot within the fuser system) to cause it to coalesce
much more efficiently. In addition, it is ensured that, on removal of the heat, the
system reverts to its bulk properties, leaving minimal residues on the machine and
the minimum of undesirable residue on the surface. It is specially important that
the final image does not feel 'sticky' to the touch, and has no unpleasant chemical
feel or smell. It is a particular feature of this invention that the heat activation
step is reversible and achieves these "user friendly" aims.
[0018] In an electrographic machine, the fusing system is specifically designed to cope
with semi-solids - the toner particles themselves are partially melted. However, it
has only a certain latitude so it is important in the implementation of this invention
that the chemical system does not cause the layer and the toner to adhere to the fusing
rollers. This requires a suitable choice of the polymers and additives to the coating.
[0019] As an aid to reducing the tendency of the system to adhere to the fusing rollers,
it is possible to include inert solid particles within or on the surface of the film.
It has been found that these particles can confer extra benefits:
(a) they can minimize the effects of any residual chemical on the surface by improving
the 'feel' of the final imaged substrate;
(b) they can act as a reservoir that releases the chemical blend when heating and
re-absorbs it on cooling; and
(c) they can provide controlled scattering to further increase image contrast.
[0020] Should users so require, the carrier substrate can be translucent to give the additional
benefits of the scattering systems.
[0021] The advantages which can be achieved by the use of a toner coalescing agent are:
(a) improved, 'stronger' images for ordinary use;
(b) improved, higher contrast overhead transparencies; and
(c) improved usability as film positives or negatives for the printing industry.
[0022] Tests confirming the mechanism of action of this invention have included:
(a) demonstrations that the effect depends on the thickness of the coating layer,
the thicker the coating (up to a limit), the stronger the image enhancement, showing
that the effect is not due merely to residual surface toner-coalescing agent;
(b) demonstrations that the toner-coalescing agent requires heat for its action e.g.
a drop of a typical agent (Citroflex A-4, a citrate plasticiser) on a non-enhanced
toner image had no effect after several hours at room temperature, but coalesced the
image rapidly when heated;
(c) demonstrations using different grades of "Syloid" filler with different oil absorption
coefficients (0.8g/g and 2g/g respectively) showed an enhanced effect using the filler
with the higher absorption coefficient; and
(d) acceptability tests showing that the feel of a test sample that had deliberately
been coated with a thin layer of "Citroflex A-4", was disliked, yet the feel of a
film that had been enhanced using "Citroflex A-4" within the coating layer was not
disliked.
[0023] The base layer preferably comprises polyethylene terephthalate or polycarbonate.
Advantageous also are base layers which comprise a pre-stabilised polyester, for example
a polyester film which has been shrunk under the influences of tension and elevated
temperature. Such a pre-stabilised film may have a dimensional stability of no more
than 2 or 3% at a temperature of 150°C.
[0024] Preferably, the base layer has a film thickness of 50 to 100 µm, onto which is coated
the optional adhesive layer which can comprise a linear polyester resin coated from
an organic solvent, the linear polyester resin preferably being coated at from 2 to
15 wt.% of the solvent.
[0025] The film-coating layer preferably has a film thickness of 10 to 20 microns which
may be coated from a solvent-based or from a water-based formulation comprising a
film-forming component, a toner-coalescing agent and an optional anti-blocking layer.
[0026] A preferred embodiment of the substrate comprises either (a) an antistatic back coat,
with a film thickness of less than 3 µm, on the outer side of the base layer, to aid
film sheet feeding through the electrostatic printer, to sharpen-up images, to prevent
the final film-coatings from sticking to one another and to minimise static build-up,
or (b) an antistatic component built into the base layer. The antistatic component
may comprise a polystyrene sulphonate or a quaternary ammonium polymeric alkyl or
aryl sulphonate compound.
[0027] When the film-coating layer is coated from a solvent-based formulation the film-forming
component preferably comprises one or more of the following polymers: nitrocellulose,
polyvinyl chloride, styrene/acrylate copolymers, polyurethanes and polyacrylonitriles.
When the film-coating layer is coated from a water-based formulation the film-forming
component preferably comprises one or more of the following polymers: polvinyl alcohol
and its derivatives, gelatin and its derivatives, cellulose derivatives, modified
starches and polyacrylamides. The film-forming component is preferably present in
a total amount of 50 to 90 wt.% of the film-coating layer.
[0028] The toner-coalescing agent is present so as to coalesce the toner, and comprises
preferably a solid plasticiser of high melting point or a liquid plasticiser of high
boiling point, which will coalesce the toner at temperatures greater than ambient.
Preferably, the toner-coalescing agent has no significant effect on the degree of
toner coalescence at temperatures up to 100°C and has a significant toner-coalescing
effect at a temperature of 120°C. In other words, the temperature at which the toner-coalescing
agent becomes effective preferably lies in the range of from 100°C to 120°C, although
the effectiveness may increase over a range of temperatures falling between these
limits.
[0029] The toner-coalescing agent preferably comprises one or more of the following chemical
compounds: dibasic polymeric polyester plasticisers, citrate plasticisers, p-toluenesulphonamide
plasticisers, benzoate plasticisers, alkyl and aryl phosphates or phthalates e.g.
dioctylphthalate, chlorinated polyolefins, or other compounds capable of coalescing
the toner. The toner-coalescing agent is preferably present in a total amount of 10
to 50 wt.% of the film-coating layer, more preferably 20 to 45 wt.%, most preferably
25 to 40 wt.%. Optionally, when the film-coating layer is a water-based formulation,
it further comprises a toner-coalescing agent containment agent which functions: to
contain the toner-coalescing agent within the film-coating layer, as a film strengthening
agent and as adhesion promoter to the optional adhesive layer. The toner-coalescing
agent containment agent preferably comprises a polyvinyl acetate polymer in a total
amount of 10 to 60 wt.% of the film-coating layer.
[0030] The anti-blocking layer preferably comprises one or more of the following solid particle
fillers: silicas, organically or inorganically treated silicas, talc, urea formaldehyde
condensates and aluminas, or other materials which can absorb the toner-coalescing
agent. The anti-blocking layer preferably comprises a solid particle filler in a total
amount of 3 to 25 wt.% of the film-coating layer.
[0031] The substrate is preferably transparent to light over the wavelength range of from
300 nm to 700 nm, preferably 350 nm to 500 nm.
[0032] The invention also provides a method of producing a film positive or negative, comprising
providing a substrate as referred to above, and
imaging the film-coating layer of the substrate with toner applied in an electrographic
printing process,
wherein the electrographic printing process includes a fusing step, in which heat
is applied to the toner-imaged substrate and has a toner-coalescing effect on the
toner forming the image.
Examples
[0033] The present invention is illustrated by the following examples whilst not being limited
thereto. In these examples, various commercially-available materials are listed by
their trade names, the letters identifying the following companies:
(a) Toray Plastics, France
(b) Huls, UK
(c) Croxton and Garry, UK
(d) Croda, UK
(e) W R Grace, UK
(f) Autotype International, UK
(g) Eastman Chemicals, USA
(h) Nippon Gohsei, Japan
(i) Resadhesion, Hants., UK
(j) Folex Film Systems, Switzerland
(k) Velsicol Chemical Corp., USA
(l) Dick Peters BV, Netherlands
(m) ICI, UK
(n) Sericol, UK
[0034] Example 1 involves a solvent-based formula whereas Examples 2, 4 and 5 involve a
water-based formula. All amounts given are on a percent by weight basis, unless stated
otherwise.
Example 1
Solvent based formula
[0035] On to a 100 µm antistatic polyester base - "Terphane 45:32" (a), an adhesive layer
of the following formulation was coated.
Butanone |
93 |
"Dynapol L411" (b) - linear polyester |
7 |
[0036] The solution was coated onto the polyester with a 0.010" Meyer bar and dried at 40°C.
[0037] To the above base plus adhesive the following coating was applied using a 0.020"
Meyer bar:
30 wt.% solution of 1/2 second Nitrocellulose in Butanone |
77.4 |
"Paraplex G-30" (c) - dibasic polyester plasticiser |
13.6 |
"Citroflex A-4" (d) - citrate plasticiser |
4.5 |
"Syloid ED-30" (e) - organically treated silica |
4.5 |
[0038] The coating was dried at 40° C. The film was imaged on a QMS 860 laser printer. The
UV density of the image was measured on a MacBeth TR927 densitometer with the following
results;
Image Density |
2.60 - 2.80 |
Background Density |
0.06 |
[0039] The film was used as film positive to image a screen stencil using "Capillex 25"
(f) - a diazo sensitised screen capillary film. The exposure was carried out in a
vacuum frame with a 5kW light source at a distance of one metre for 5 minutes. After
exposure the screen stencil was developed by washing in a cold water spray. The stencil
was dried and the image examined for quality. The image density achieved was equivalent
to a conventional silver halide film positive.
[0040] The stencil was printed to 1,000 impressions on a Svecia screenprinting press using
Mattplast MG (n) inks with no apparent signs of image breakdown.
Comparative Example 1
Solvent based formula
[0041] The procedure of Example 1 was repeated exactly, except that "Paraplex G-30" and
"Citroflex A-4" were omitted from the coating solution.
[0042] The U.V. density of the image was as follows:
Image Density |
1.50 - 1.80 |
Background Density |
0.16 - 0.20 |
[0043] As in Example 1, the imaged positive was used to make a Capillex 25 screen stencil.
The resulting stencil resisted washout development in the clear areas. These areas
correspond to the weak image generated in this comparative example. The positive was
insufficiently dense to prevent UV light passing through and partially exposing the
Capillex stencil. The developed stencil was of such poor quality that it was not suitable
for printing from.
Example 2
Water based formula
[0044] On to a 100 µm antistatic polyester base - "Terphane 45:32" (a), an adhesive layer
of the following formulation was coated.
Water/IPA (1:1) |
95 |
30 wt.% "Aq. 29D" (g) - sulphonated linear polyester |
5 |
[0045] The solution was coated onto the polyester with a 0.0060" Meyer bar and dried at
40°C.
[0046] To the above base plus adhesive the following coating was applied using a 0.020"
Meyer bar:
10 wt.% "Gohsenol GH-20" (h) - polyvinyl alcohol aq. solution |
62.0 |
50 wt.% "Resad 1350" (i) - stabilised polyvinyl acetate |
25.0 |
Paraplex G-30 |
6.2 |
Citroflex A-4 |
3.1 |
Syloid ED-30 |
3.7 |
[0047] The film was formed and treated in a similar manner to Example 1 above. The density
of the final image achieved was equivalent to a conventional silver halide film positive.
Comparative Example 2
Water based formula
[0048] The procedure of Example 2 was repeated exactly, except that "Paraplex G-30" and
"Citroflex A-4" were omitted from the coating solution.
[0049] The U.V. density of the image was as follows:
Image Density |
1.60 - 1.70 |
Background Density |
0.10 - 0.20 |
Example 3
[0050] Commercially available laser imageable films - "Delta Laser Film" (f) and "Folaproof
Laserfilm" (j) were imaged on a QMS 860 laserprinter in a similar manner to Example
1 above. In each case the U.V. density of the image was as follows:
Image Density |
1.60 - 1.70 |
Background Density |
0.10 - 0.20 |
Example 4
Water based formula
[0051] On to a 100 µm antistatic polyester base - "Terphane 45:32" (a) - an adhesive layer
of the following formulation was coated.
Water/IPA (1:1) |
95 |
30% "Aq. 29D" (g) - sulphonated linear polyester |
5 |
[0052] The solution was coated on to the polyester with a 0.0060" Meyer bar and dried at
40°C.
[0053] To the above base plus adhesive the following coating was applied using a 0.020"
Meyer bar:
10% "Gohsenol GH-20" (h) |
61.3 |
50% "Resad 1350" (i) |
24.5 |
"Benzoflex 2-45" (k) - diethylene glycol dibenzoate plasticiser |
9.2 |
"Syloid C-906" (e) - organically treated silica |
5.0 |
[0054] The film was formed and treated in a similar manner to Example 1 above.
[0055] The measured U.V. density was as follows:
Image density |
2.50 - 2.90 |
Background Density |
0.10 - 0.20 |
[0056] The image density achieved was equivalent to that of a conventional silver halide
film positive.
Example 5
Water based formula
[0057] To the adhesive-layer coated polyester base prepared according to Example 4, the
following coating was applied using a 0.040" Meyer bar:
10% "Gohsenol GH-20"(h) |
56 |
50% "Resad 1350" (i) |
22 |
"Benzoflex 9-88" (k) - dipropylene glycol dibenzoate plasticiser |
3 |
"Cereclor S-63" (m) - chlorinated polyolefin plasticiser |
11 |
"Syloid E02" (e) - organically treated silica |
2 |
30% "Permanol HN2" - high density polyethylene dispersion |
7 |
[0058] The film was formed and treated in a similar movement to Example 1 above.
[0059] The measured U.V. density was as follows:
Image density |
2.50-2.90 |
Background density |
0.10-0.20 |
[0060] The image density achieved was equivalent to that of a conventional silver halide
film positive.
Example 6
[0061] The adhesive layer formulation of Example 2 was coated at a thickness of 10 µm on
a sheet of Autostat CT4 (f) pre-stabilised polyester film base of 100 µm thickness.
The coating formulation of Example 5 was then coated onto the adhesive layer at a
thickness of 10 µm. The length of the sheet was measured using a Maxtascan 250 XY
plotting microscope before and after imaging on a Xante 8300 laser printer. The following
results were obtained:
original length of sheet (mm) |
length after processing (mm) |
% change |
297.20 |
296.41 |
0.266 |
[0062] The change in length during processing using a standard laser printer is sufficiently
small to maintain the integrity of the imaged film. This is particularly desirable
when four-colour process work is to be carried out.
Example 7
[0063] The following tests were conducted to illustrate the effect of different levels of
plasticiser addition.
[0064] A base mix was made in the following formulation, the quantities being in grams:
10 wt % Gohsenol GH20 (h) |
470 |
50 wt% Resad 1350 (i) |
190 |
Syloid ED 30 (e) |
75 |
30 wt% Permanol HN2 (l) |
15 |
water |
250 |
[0065] The mixture was divided into six equal parts and the following additions of Benzoflex
9-88 (k) and Cereclor S-63 (m) were made using a 2:1 ratio mix of the two plasticisers.
part number |
Benzoflex 9-88 |
Cereclor S-63 |
% addition of plasticiser |
1 |
0.00 |
0.00 |
0 |
2 |
1.32 |
2.64 |
9.80 |
3 |
3.30 |
6.67 |
21.3 |
4 |
3.96 |
8.04 |
24.5 |
5 |
6.60 |
13.4 |
35.2 |
6 |
9.90 |
20.1 |
44.9 |
[0066] The coating and film-treatment steps of Example 5 were repeated for each of the six
mixtures and the following UV image density values were obtained by interpolation
of the results.
plasticiser level |
0% |
10% |
15% |
20% |
30% |
35% |
40% |
45% |
UV density |
1.65 |
1.76 |
1.86 |
2.07 |
2.33 |
2.47 |
2.59 |
2.72 |
1. A substrate for use in producing film positives by means of an electrographic printing
process, the substrate comprising:
a base layer, an optional adhesive layer and a film coating layer, the film-coating
layer having within its bulk a toner-coalescing agent which, under the influence of
the heat of the fusing step of the electrographic printing process, has an effect
of improving the degree of coalescence of the toner applied to the surface of the
film-coating layer.
2. A substrate according to claim 1, wherein the film-coating layer has a film thickness
of 10 to 20 µm.
3. A substrate according to claim 1 or 2, wherein the bases layer comprises a pre-stabilised
polyester.
4. A substrate according to claims 1 or 2, wherein the base layer comprises polyethylene
terephthalate or polycarbonate.
5. A substrate according to any preceding claim, wherein the base layer has a film thickness
of 50 to 100 µm.
6. A substrate according to any preceding claim, having (a) an antistatic back coat,
on the side of the base layer opposite the film-coating layer, or (b) an antistatic
component incorporated in the base layer.
7. A substrate according to claim 6, having an antistatic back coat having a thickness
of less than 3 µm.
8. A substrate according to claim 6, having an antistatic component incorporated into
its base layer, the antistatic component comprising a polystyrene sulphonate or a
quaternary ammonium polymeric alkyl or aryl sulphonate compound.
9. A substrate according to any preceding claim, wherein the film-coating layer is a
solvent-based or a water-based formulation comprised of a film-forming component,
a toner-coalescing agent and/or an anti-blocking layer.
10. A substrate according to claim 9, wherein the anti-blocking layer comprises a solid
particle filler in a total amount of 3 to 25 wt.% of the film-coating layer.
11. A substrate according to claim 9, wherein the film-coating layer is a solvent-based
formulation and the film-forming component comprises one or more of the following
polymers:
nitrocellulose;
polyvinyl chloride;
styrene/acrylate copolymers;
polyurethanes; and
polyacrylonitriles.
12. A substrate according to claim 9, wherein the film-coating layer is a water-based
formulation and the film-forming component comprise one or more of the following polymers:
polyvinyl alcohol and its derivatives;
gelatin and its derivatives;
cellulose derivatives;
modified starches; and
polyacrylamides.
13. A substrate according to any preceding claim, wherein the toner-coalescing agent has
no significant effect on the degree of toner coalescence at temperatures up to 100°C
and has a significant toner-coalescing effect at a temperature of 120°C.
14. A substrate according to any preceding claim, wherein the toner-coalescing agent is
present in an amount of 10 to 50 wt.% of the film-coating layer.
15. A substrate according to claim 14, wherein the toner-coalescing agent is present in
an amount of 20 to 45 wt.% of the film-coating layer.
16. A substrate according to any preceding claim, wherein the toner-coalescing agent comprises
one or more of the following chemical compounds:
dibasic polymeric polyester plasticisers;
citrate plasticisers;
p-toluenesulphonamide plasticisers;
benzoate plasticisers e.g. triethyleneglycol or tripropyleneglycol dibenzoate;
alkyl and aryl phosphates; and
chlorinated polyolefins.
17. A substrate according to claim 10, wherein the anti-blocking layer comprises one or
more of the following solid particle fillers:
silicas;
organically or inorganically treated silicas;
talc;
urea formaldehyde condensates; and
aluminas;
or other materials which can absorb the toner-coalescing agent.
18. A substrate according to claim 11, wherein the film-coating layer is a water based
formulation and further comprises a toner-coalescing agent containment agent which
functions to contain the toner-coalescing agent within the film-coating layer, as
a film strengthening agent and/or an adhesion promoter to the optional adhesive layer.
19. A substrate according to claim 18, wherein the toner-coalescing agent containment
agent comprises a polyvinyl acetate polymer in a total amount of 10 to 60 wt.% of
the film-coating layer.
20. A substrate according to any preceding claim, having an adhesive layer comprising
a linear polyester resin coated from an organic solvent.
21. A substrate according to claim 20, wherein the linear polyester resin is coated at
from 2 to 15 wt.% of the solvent.
22. A substrate according to any preceding claim, wherein the film-forming component is
present in a total amount of 50 to 90 wt.% of the film-coating layer.
23. A substrate according to any preceding claim, which is transparent to light over the
wavelength range of from 300 nm to 700 nm, preferably 350 nm to 550 nm.
24. A method of producing a film positive or negative, comprising:
providing a substrate according to any preceding claim, and
imaging the film-coating layer of the substrate with toner applied in an electrographic
printing process,
wherein the electrographic printing process includes a fusing step, in which heat
is applied to the toner-imaged substrate and has a toner-coalescing effect on the
toner forming the image.