FIELD OF THE INVENTION
[0001] This invention relates to photographic elements sensitive to light emitted in the
near-infrared portion of the spectrum, from 750 nm and above, especially 750 to 1500
nm, and in particular to photographic elements adapted to provide a high quality recording
medium for laser diode scanning systems.
BACKGROUND OF THE INVENTION
[0002] A widely used image processing technique is to convert a visible image into electronic
data by encoding the brightness of adjacent small areas of the visible image. Such
electronic encoding is advantageous for manipulation, transmission and storage of
images. It is known to reconvert electronic data into visible images by means of a
so-called "scanner system" whereby a finely focussed beam of light is rapidly scanned
across a light sensitive medium in a succession of abutting raster lines, whilst modulating
the intensity of light so as to reproduce the required image densities, based on the
electronic signals.
[0003] Lasers, especially those using argon, krypton, helium-neon or helium-cadmium mixtures
as the gas lasing media, have been used as sources of high intensity light for this
imaging technique. However, the lasers all suffer the disadvantage of requiring an
additional, complex device to modulate the intensity of light emitted, and to a greater
or lesser extent, from large physical bulk, mechanical fragility and expense of manufacture.
[0004] Semiconductor laser diodes are potentially highly suitable as light sources for scanner
systems in that their light output can be directly modulated by the electrical signal
input, and that they are very compact and physically durable.
[0005] However, at present the only commercially available laser diode devices to have acceptably
long operational life-times, and be capable of cheap manufacture, are those emitting
light in the near-infrared (NIR) portion of the spectrum, from 750 to 1500 nm. Accordingly,
in order to utilize laser diode scanner systems for imaging purposes it is necessary
to provide a recording medium which is sensitive to light in the NIR range.
[0006] It is known to spectrally sensitise photographic silver halide emulsions to near-infrared
light, using long chain cyanine dyes, see, for example, Mees and James, The Theory
of the Photographic Process, 3rd Edition, MacMillan, 1966, pp. 198-201 and references
cited therein.
[0007] It has been found that NIR sensitised photographic films, especially those having
silver halide grains of mean diameter less than 0.4 micron, when supported by the
edges in a glassless holder, to prevent contact with other surfaces, and given a uniform
overall exposure from a laser diode scanner system emitting at 820 nm, produce images
covered with broad swirling interference patterns, referred to hereinafter as "non-contact
scanner fringes'. These fringes are believed to arise as a result of the reflection
of the exposing light from the two interfaces of the film element with surrounding
air. The path difference between the rays reflected from the top surface of the film
and the bottom surface is controlled by the thickness of the film at a given point,
and the net phase difference causes either destructive or constructive interference,
causing either diminished or increased exposure to be transmitted into the light sensitive
emulsion layer at that given point. The fringes therefore follow contours of microscopic
thickness variation in the film element itself, and cover the whole of the image area
with broad lines usually about 1 mm apart and often several centimetres in length.
[0008] Non-contact interference fringes have not previously been reported in the literature
in relation to silver halide emulsion materials. This phenomenon does not occur under
the normal conditions of exposure with visible light because the turbidity of the
photosensitive emulsion layer is sufficient to scatter the reflections from the back
of the film element. However, because of its longer wavelength, infrared light is
able to pass without serious scattering through small-grained photographic emulsions,
and the coherence of the laser diode output enhances the tendency to form interference
patterns. Thus, a photographic emulsion having silver halide grains of mean diameter
0.28 micron, with a coating weight of silver of 3 g/m
2, shows detectable fringes. Lowering the grain size to 0.23 micron or reducing the
coating weight causes more noticeable patterns, whilst emulsions of mean grain diameter
0.20 micron or less exhibit severe fringes after non-contact laser diode scanning.
[0009] Non-contact scanner fringes seriously degrade the quality of scanner images, especially
those having continuous tone gradation. They are not only aesthetically displeasing
but they also obscure important information conveyed by small density differences
in the image. It is desirable to be able to use photographic.emulsions having grains
of mean diameter less than 0.4 micron preferably less than 0.30 micron. Fine grain
emulsions having a grain size of 0.4 micron or less are advantageous in permitting
high spatial resolution, and in having high covering power, permitting a lower coating
weight of silver to produce a given maximum optical density after development. Accordingly,
photographic elements for use with laser diode scanning systems must be capable of
suppressing non-contact interference fringes.
[0010] The phenomenon of interference fringes is not unknown in optical recording systems.
When exposing shiny surfaced photographic films in contact with other shiny surfaces,
e.g. glass supports, dot screens or contact printing negatives, a common problem is
the occurrence in the developed image of closely spaced concentric fringe patterns,
known as "Newton's rings", see, Encyclopedic Dictionary of Physics, J. Thewlis, Ed.,
Pergamon, London, 1961, p. 878. These fringes arise due to optical interference between
reflections from the top surface of the film and the bottom surface of the contacting
support; the size of the local air gap determines the path difference between these
two sets of rays, and hence whether their phase difference gives rise to a light or
dark fringe causing additional or diminished exposure to be transmitted into the emulsion
layer. Newton's rings tend to form isolated areas of pattern, radiating concentrically
from the points of contact during exposure, with a narrow fringe spacing which becomes
progressively smaller towards the edge of each pattern. These are quite different
in appearance to the broad swirling non-contact scanner fringes which cover the whole
image area with broad lines usually about 1 mm apart and often several centimetres
in length.
[0011] Methods are known in the art to prevent formation of Newton's rings. For example,
it is known to incorporate matting particles in the outer surface of films. Examples
of known matting particles include silica, poly-methyl methacrylate (PMMA), other
polyvinyl compounds including copolymers, starch or inorganic salts. The density of
matting coverage varies from a relatively small number (e.g. applied at less than
0.1 g/m
2) of fairly large particles usually 5 to 10 micron in diameter as disclosed in United
States Patent Specification Nos. 4 235 959, 4 022 622, 3 754 924 and 2 322 037, to
a particle weight of greater than up to 1 g/m
2 or 50% of the topcoat binders as disclosed in British Patent Specification Nos. 2
077 935 and 2 033 596 and United States Patent Specification Nos. 3 507 678 and 2
992 101 utilizing smaller particle sizes.
[0012] Use of visible laser light as illumination for contact screen exposure of both emulsions
produces particularly severe Newton's rings fringes.. United States Patent Specification
No. 4 343 873 discloses a photographic element designed to minimise such fringes which
includes a light-scattering layer through which the light-sensitive layer is exposed
to laser light. The light-scattering particles have a diameter of from 50 to 150%
of the wavelength of the illuminating laser. The light scattering layer may be coated
as an outer layer on the photographic element or beneath other layers.
[0013] It is also known to use matting agents in photographic elements for non-optical properties,
such as resistance to adhesion, abrasion resistance, retouchability, good draw-down
in vacuum frames, and reduced static effects. An example of the use of a matting agent
is an infrared sensitive film is disclosed in United States Patent Specification No.
4 266 010 which describes an emulsion topcoat containing PMMA of size in the range
0.2 to 10 micron in an acid-processed gelatin binder, stating this to be suitable
for all types of photographic materials including infrared films. A further example
is disclosed in United States Patent Specification No. 3 695 888 which describes a
photographic emulsion sensitised to infrared light by cyanine dyes with mesoalkylamino
substituents and specific super- sensitisers, stating that such elements can contain
matting agents such as starch, titanium dioxide, zinc oxide, silica, polymeric beads,
including 1 to 4 micron beads of a methacrylic acid-methyl methacrylate copolymer
disclosed in United States Patent Specification No. 2 992 101 and 1 to 20 micron poly-methyl
methacrylate beads formed by emulsion polymerisation as disclosed in United States
Patent Specification No. 2 701 245.
[0014] It has been found that the known types of layers used on photographic elements for
suppressing Newton's rings do not prevent the formation of non-contact interference
fringes for photographic elements having a photographic emulsion of fine grain size
sensitised to the near-infrared.
BRIEF DESCRIPTION OF THE INVENTION
[0015] According to the present invention there is provided a photographic element comprising
a support transparent to near infrared radiation above 750 nm, generally in the range
750 to 1500 nm, one or more layers of a silver halide emulsion having grains of an
average diameter of not more than 0.4 micron, sensitised to near infrared radiation,
characterised in that the element comprises one or more of:
(i) a topcoat layer which is an outermost layer on the same side of the support as
the photosensitive emulsion which topcoat layer is a diffuse transmitting layer with
respect to near infrared radiation,
(ii) a backing layer which is an outermost layer on the side of the support remote
from the photosensitive emulsion which backing layer is a diffuse reflecting layer
or absorbing layer with respect to new infrared radiation,
(iii) a subbing layer which is positioned between the support and the photosensitive
emulsion which subbing layer is a diffuse transmitting or absorbing layer with respect
to near infrared radiation, whereby the element may be imaged by a laser scanning
system emitting near infrared radiation substantially without formation of non-contact
interference fringes.
[0016] A photographic element in accordance with the invention is resistant to the formation
of internal optical interference patterns which cause unprotected fine grain near-infrared
films to become covered in broad swirling fringes when processed after scanning with
a laser diode NIR light source, despite non-contact of the film with other surfaces
during exposure.
[0017] Three main techniques have been found for preventing formation of non-contact interference
fringes, which techniques may be used alone or in combination.
[0018] It has been found that the microscopic surface roughness of the element can play
an important part in inhibiting the formation of interference fringes. A microscopic
surface roughness having 200,000 protrusions per square millimetre provides a marked
reduction in the formation of interference fringes and a surface roughness on the
backside of the film having 250,000 protrusions per square millimetre will substantially
completely eliminate interference fringes, as will a surface roughness of more than
250,000, preferably, 450,000 protrusions per square millimetre on the top surface.
[0019] A second technique of inhibiting the formation of interference fringes is to provide
a backing or subbing layer containing a dye absorbing light in the wavelength range
of the exposing source. When such a layer is used alone as fringe suppression layers
of the invention means the layer should have a peak transmission optical density of
at least 0.75; when such a layer is used in combination with other fringe suppression
means an optical density of at least 0.3 will make a significant contribution to the
fringe reduction.
[0020] The third technique for reducing fringe formation employs a backing and/or topcoat
layer comprising a binder containing particles having a high refractive index substantially
preferably greater than 0.3 larger than that of the binder, e.g. desensitised silver
halide particles in gelatin.
[0021] The use of silver halide particles is advantageous as the halide may be removed during
the processing of the photographic element. The high refractive index layer may desirably
be removed subsequent to exposure, such as by applying a solvent for the binder.
[0022] It has been found that there are several constructions of fine grain near-infrared
sensitive photographic elements which will substantially completely suppress the formation
of non-contact interference fringes. For example, non-contact interference fringes
may be suppressed in such photographic elements incorporating one or more of the methods
in the following constructions:
(1) A backing layer on the side of the film base remote from the photosensitive emulsion,
comprising a binder containing a surface roughening agent having average particle
size not more than 2 micron, generally in the range 0.1 to 2 micron and preferably
0.2 to 2 micron, this outer backing layer having a microscopic roughness of the outer
surface, such that each square millimetre of that surface contains at least 250,000
particles which protrude above the average level of that surface by at least 30% of
their individual diameters, or by 0.2 micron, whichever is less.
(2) A topcoat layer on the same side of the film base as the photosensitive emulsion,
comprising a binder containing a surface roughening agent having average particle
size not more than 1.5 micron, generally in the range 0.1 to 1.5 micron, and preferably
0.2 to 1.5 micron, this topcoat layer having a microscopic roughness of the outer
surface, such that each square millimetre of that surface contains at least 250,000
preferably at least 450,000 particles which protrude above the average level of that
surface by at least 30% of their individual diameters, or by 0.2 micron, whichever
is less.
(3) A backing or subbing layer containing an antihalation dye absorbing light above
750 nm, preferably in the wavelength range 750 to 1500 nm and having a peak transmission
optical density of at least 0.75, in that region.
(4) An outermost backing layer containing an antihalation dye giving a peak transmission
optical density of at least 0.3 with respect to light above 750 nm, preferably in
the wavelength range 750 to 1500 nm, and containing a surface roughening agent of
average particle size not more than 2 micron, generally in the range 0.1 to 2 micron,
and preferably 0.2 to 2 micron, this layer having a microscopic roughness of the outer
surface such that each square millimetre of that surface contains at least 200,000
particles which protrude above the average level of that surface by at least 30% of
their individual diameters, or by 0.2 micron, whichever is less, this layer optionally
being divided into two separate layers, an outermost backing layer containing the
surface roughening agent and the inner backing layer containing the antihalation dye.
(5) The combination of a backing layer having a peak transmission optical density
of at least 0.3 with respect to light above 750 nm, preferably in the wavelength range
750 to 1500 nm, and an outermost topcoat layer containing a surface roughening agent
having an average particle size not more than 2 micron, generally in the range 0.1
to 2 micron, and preferably 0.2 to 2 micron, this layer having a microscopic roughness
of the outer surface such that each square millimetre of that surface contains at
least 200,000 particles which protrude above the average level of that surface by
at least 30% of their individual diameters, or by 0.2 micron, whichever is less.
(6) The combination of an antihalation layer having a peak transmission optical density
of at least 0.3 with respect to light above 750 nm, preferably in the wavelength range
750 to 1500 nm, positioned between the photosensitive layer and the base, and an outermost
backing layer or topcoat layer containing a surface roughening agent having an average
particle size not more than 2 micron, generally in the range 0.1 to 2 micron, and
preferably between 0.1 to 2 micron, this layer having a microscopic roughness of the
outer surface such that each square millimetre of that surface contains at least 200,000
particles which protrude above the average level of that surface by at least 30% of
their diameters, or by 0.2 micron, whichever is less.
(7) A topcoat layer containing a surface roughening agent having an average particle
size not more than 2 micron generally in the range 0.1 to 2 micron add preferably
between 0.2 to 2 micron, this layer having a microscopic roughness of the outer surface
such that each square millimetre of that surface contains at least 200,000 particles
which protrude above the average level of that surface by at least 30% of their individual
diameters, or by 0.2 micron, whichever is less, in combination with an outermost backing
layer containing a surface roughening agent having an average particle size not more
than 2 micron generally in the range 0.1 to 2 micron and preferably between 0.2 to
2 micron, this layer having a microscopic roughness of the outer surface such that
each square millimetre of that surface contains at least 200,000 particles which protrude
above the average level of that surface by at least 30% of their individual diameters,
or by 0.2 micron, whichever is less, and optionally a layer positioned between the
backing layer and the support containing an antihalation dye providing a peak transmission
optical density of at least 0.3 with respect to light above 750 nm, preferably in
the wavelength range 750 to 1500 nm.
(8) A backing and/or topcoat layer comprising a binder containing particles having
a refractive index substantially larger than that of the binder (e.g. non-sensitised
silver halide particles) said particles having an average particle size below 5 micron
and preferably 0.2 to 3 micron, the layer being removable during photographic processing.
[0023] It has been found that the microscopic roughness of the photographic element markedly
affects the propensity of the element to form non-contact interference fringes when
imaged with a scanning laser. In particular, it has been found that the provision
of an outer backing layer providing a microscopic roughness having at least 250,000
protrusions per square millimetre above the average level of the surface will prevent
fringe formation, assuming irradiation takes place from the other side of the element.
Similarly, fringe formation can be prevented by provision of a topcoat layer the microscopic
surface roughness providing at least 250,000 preferably 450,000 protrusions per square
millimetre assuming the element is irradiated from the same side as this layer. This
microscopic surface roughness is significantly different from that found in prior
art photographic elements incorporating layers of matting agents; in general matting
layers in the prior art tend to provide surfaces with less than half the number of
protrusions than those required in the present invention and often contain less than
one tenth of the number of protrusions than the surfaces used in the invention.
[0024] It is possible to substantially suppress fringe formation by employing a backing
or subbing layer incorporating an antihalation dye to provide a peak transmission
optical density of at least 0.75 in the range 750 to 1500 nm.
[0025] Combinations of surface roughening layers and antihalation layers may be employed
as described above in which case the critical parameters of surface roughening and
optical density for each individual layer may be reduced compared to that required
when such layers are used as the only means for reducing fringe formation since the
effect of the combination of layers is additive. It has been found that a suitable
microscopic surface roughness for an outer layer to be used in combination with a
further fringe suppressing layer is 200,000 protrusions per square millimetres the
optical density required by an antihalation layer to be used in combination with a
Surface roughening layer is at least 0.3
[0026] Particle -containing surface layers described above are preferably used on the back
surfaces of the elements, or on both outermost surfaces, rather than as topcoats on
the photosensitive emulsion side only , since, surprisingly the suppression of non-contact
laser scanner fringes by surface roughened backings is superior to that by similar
topcoats on the emulsion side assuming the exposure is from the emulsion side.
[0027] Advantageous surface roughening agents for use in such layers are particles of organic
polymers, particulary of polymethyl methacrylate or developer - soluble polymers such
as methacrylie acid - methacrylie ester ecpolymers e.g as described in United States
Patent Specification No. 2 992 101. Other suitable organic polymers, when used in
the particle size range, and loading needed to give the matting properties specified
above, are other polyvinyl compounds or vinyl compound copolymers, e.g. as described
in British Patent Specification Nos. 2 078 992 and 2 033 596 and United States Patent
Specification Nos. 4 287 299 and 3 079 257. Other suitable materials include silica
or composites of silica with polymer, e.g. as described in United States Patent Specification
Nos. 4 235 959, 3 920 456, 3 591 379 and 3 222 037, hardened gelatin, water soluble
inorganic salts, or starch, dextran and mixtures of these polymers, as described in
British Patent Specification No. 2 077 935.
[0028] One type of matting agent known in the art consists of very small particles of silica,
typically of diameter 0.1 micron or less. On dispersion in coating binders such as
aqueous gelatine, these small particles form tightly-bound aggregates, typically of
1 micron or greater in diameter, which behave as though they were a single particle.
The matting properties required for the purposes of this invention may be obtained
either by the use of single particles in the required size range, or equally by use
of aggregates, the overall size of which falls in the same required range.
[0029] Suitable materials of high refractive index include non-photosensitive silver halide
crystals, which are readily produced in uniform sizes and removed by photographic
fixers. Silver halides generally have a refractive index in the range 2.0 to 2.2.
Other suitable materials of high refractive index include zinc oxide and calcium carbonate.
[0030] Gelatin is a suitable binder for all these layers and has a refractive index of about
1.5.
[0031] When small polymer or other particles, especially those of mean diameter 1 micron
or below, are used to matt the surface of a layer of binder as this is coated, the
height of the protrusions above the average surface level, and the number of particles
protruding, is dependent not only on the weight of particles contained in the layer,
but also on the coating and drying conditions used. It is important to select conditions
for coating and drying which give the high degree of particle protrusion required
by this invention and these parameters will be appreciated by a person skilled in
the art. One technique which has proved to provide satisfactory surface roughness
when used with suitable formulations is to pass the wet element immediately after
coating into a chill zone at 13
0C at 30% relative humidity to cause the gel to set and thereafter to dry at 30°C,
at 30% relative humidity. It was found that the thin layers were dry in 30 seconds
to 1 minute.
[0032] In addition to the above matting particles introduced for the purposes of surface
roughening in accordance with the invention, the photographic element can contain
small quantities (less than 0.1 g/m
2) of larger polymer, silica or other matting agent with particles of mean diameter
5 micron and greater, to improve mechanical properties such as adhesion and abrasion
resistance.
[0033] Silver halide emulsions useful in the photographic elements of this invention may
comprise silver bromide, silver chloride, silver chlorobromide, silver bromoiodide
or silver chlorobromoiodide, and can be prepared by any of the well known procedures,
e.g. as described in Research Disclosure 17643, December 1978, par. II and III. The
emulsions have a particle size of not more than 0.4 micron, generally in the range
0.05 to 0.4 micron.
[0034] The emulsions can be sensitised to near-infrared using the dyes disclosed in European
Patent Application Publication No. 0 088 595, or using any of the other spectral sensitising
dyes known in the art to give sensitivity to radiation of wavelength 750 to 1500 nm,
preferably 750 to 900 nm, e.g. as described in Mees and James, The Theory of the Photographic
Process, 3rd Ed., pp. 198-199.
[0035] Silver halide emulsions present in the photographic element of this invention can
be protected against the production of fog and can be stabilised against loss of sensitivity
during keeping. Suitable antifoggants and stabilisers are described, for example,
in Research Disclosure 17643, December 1978, par. VI.
[0036] Silver halide emulsions present in the photographic elements of this invention can
employ optical brightening agents as described, for example, in Research Disclosure
17643, December 1978, par. V.
[0037] The spectrally sensitised silver halide emulsions used in the invention can contain
speed increasing compounds, e.g. those described in Research Disclosure 17643, December
1978, par. XXI.
[0038] The layers of the photographic elements can contain various colloids as vehicles
or binding agents, e.g. those described in Research Disclosure 17643, December 1978,
par. IX. Such colloids can be hardened by various organic and inorganic hardeners,
e.g. those described in Research Disclosure 17643, December 1978, par. X.
[0039] The photographic elements of the invention can contain antistatic or conducting layers,
plasticisers and lubricants, surfactants, as described, for example, in Research Disclosure
17643, December 1978, par. XI, XII and XIII.
[0040] Photographic emulsions used in the invention can be coated on a wide variety of transparent
supports, e.g. those described in Research Disclosure 17643, December 1978, par. XVIII.
[0041] The sensitising dyes and other emulsion addenda can be incorporated into the layers
of the photographic elements by various methods known in the art, e.g. those described
in Research Disclosure 17643, December 1978, par. XIV. Similarly the photographic
elements can be coated on photographic supports by various procedures. Supports and
coating procedures are described, for example, in Research Disclosure 17643, December
1978, par. XV and XVII.
[0042] The sensitised silver halide emulsions used in this invention can be processed after
exposure to form a visible silver and/or dye image by associating the silver halide
with an aqueous alkaline medium in the presence of a developing agent as described,
for example, in Research Disclosure 17643, December 1978, par. XIX.
[0043] Whilst this invention is described in detail for elements containing silver halide
grains below 0.4 micron in diameter, the methods for fringe suppresssion are equally
applicable to elements containing other photosensitive silver halide crystals which
may permit formation of scanner fringes due to low turbidity. In particular the invention
is applicable to elements containing tabular grains of silver halide exceeding 0.4
micron in diameter, but of high aspect ratio, especially if these are present as a
low overall fraction of the silver halide grains in the element, the remainder being
comprised of fine grains.
[0044] The photographic elements of this invention can be useful in physical development
systems, image transfer systems, dry development systems, diffusion transfer systems,
printing and lithography, print-out and direct-print systems as, described, for example,
in Research Disclosure 17643, December 1978, par. XXII, XXIII, XXIV, XXV, XXVI and
XXVII. The invention will now be illustrated by the following Examples.
[0045] In the Examples the evaluation of the samples was conducted as follows:
Evaluation of Samples by Non-contact Laser Diode Scanning, and Measurement of Fringes
[0046] Samples were evaluated by uniform exposure in a scanner system in which the radiation
from a Hitachi HLP 1400 laser diode emitting at 815 nm was focused to a circular spot
of 50 microns diameter on the surface of the sample. The focused spot was scanned
in raster pattern of of 200 lines/cm over the sample by means of an oscillating galvanometer
mirror in path of the infrared beam. The intensity of the exposure was increased stepwise
to produce after processing a scale from miniminum to maximum density on the sample.
The samples were then developed using an automatic roller processor 3M type XP507
utilising Eastman Kodak RP X-Omat processing solutions. A visual inspection for fringe
patterns was made, and these assessed using the following ranking order:
1 No fringes seen
2 Almost undetectable fringes
3 Very faint, seen only under close scrutiny
4 Diffuse patterns
5 Faint, but sharply defined fringes
6 Readily noticed fringes
7 Sharply defined fringe patterns.
[0047] The fringe patterns were quantitatively evaluated by tracing with a Joyce-Loebl MDM6
microdensitometer using a small (2.0 x 0.25 mm) slit aperture. The maximum transmission
optical density difference (O.D.) thus measured between light and dark fringes is
given in the Examples. The O.D. was measured in areas scanned to mean optical density
of between 1.0 and 2.0, in which region the emulsion had contrast values of from 2.5
to 3.5.
[0048] The measurement of surface reflectivity of the samples in the Examples was conducted
as follows:
Measure of direct (specular) surface reflectivity of matted back surfaces
[0049] Samples were prepared prior to testing by physical removal of the photosensitive
emulsion layer, and by application of a densely I.R. absorbing, non-reflective layer
in its place. The untreated side of the samples was then irradiated at an angle of
10
0 to the normal with a collimated beam of known energy, of 5 mm diameter, from a laser
diode emitting at 815 nm. A radiometric detector was used to monitor the reflected
energy at a total angle of 20° to the incident beam (Optronics model 730A). This detector
was sited at a distance of 30 cm from the test surface, and admitted light through
a circular aperture of 1 cm diameter.
[0050] As the same detector was used to assess both incident and reflected energy, a simple
calculation allowed percentage reflectivity to be ascertained. Care was taken with
choice of laser diode/sample film/detector configurations to ensure that any extraneous
energy was omitted from measurements.
[0051] The examination of matted surfaces of the samples in the Examples was conducted as
follows:
Scanning electron microscope examination of matted surfaces (S.E.M.)
[0052] A sample (approximately 1 cm
2) of the film was bonded to a pin stub, with the surface to be examined uppermost.
A gold coating, approximately 25 nm thick, was applied, using an International Scientific
Instruments Inc. (ISI) PS-2 coating unit, at 1.2 kV and 10 mA for 2 minutes. The samples
were examined in an ISI Super IIIA scanning electron microscope, operating at 10 kV.
The samples were angled at +20°. In each case a photograph was taken at a print magnification
of 5000
X, using an internal calibration marker. Particle counts were made within a grid representing
an area of 10 micron x 10 micron. Particles were counted if they appeared to extend
above the average surface level by at least 30% of their diameter, or 0.2 micron,
whichever was smaller. In samples where only large, infrequent particles were present,
photographs at 2000X or lower magnification were taken, and counts made over a more
extensive area.
[0053] The results reported are an average of counts made from photographs of two different
parts of each surface examined.
Example 1
Preparation of NIR sensitive silver halide emulsions and their use in photographic
elements for laser diode scanner tests
[0054] An emulsion containing 64% silver chloride moles and 36% silver bromide moles with
cubic grains having an average grain size of 0.28 micron and a narrow distribution
curve was prepared by a double jet precipitation method described in Example 17B of
European Patent Application Publication No. 0 088 595.
[0055] Similar emulsions having mean grain sizes of 0.23 micron, 0.20 micron, 0.16 micron
and 0.13 micron were likewise prepared, using successively lower temperatures for
precipitation. All these emulsions were conventionally gold and sulphur sensitised
and stabilised, and NIR spectral sensitising dye, triphenylphosphine supersensitiser,
wetting agents and hardener were added as described in the basic formulation in Example
18 of European Patent Application Publication No.0 088 595. The emulsions were coated
individually on transparent 0.18 mm subbed polyester base, to give 2.7 to 3.0 g/m
2 silver coating weight. A supercoat of 200 ml of 5
% aqueous gelatin containing 100 mg Superamide L9C and 0.15 ml Teepol 610 wetting agents
and 4.5 ml of 2% solution of formaldehyde hardener, but no matting agents or filter
dyes, was simultaneously applied to give a top layer of 1.33 g/m
2 gelatin. The back surface of the film base was left uncoated. Superamide L9C is a
high activity lauric acid-diethanolamine condensate commercially available from Millmaster-Onyx
UK. Teepol 610 is a sodium salt of a secondary alkyl sulphate commercially available
from Shell Chemicals UK Ltd.
[0056] The samples were evaluated as described above and the results shown in Table 1.

[0057] This Example demonstrates the increasing severity of scanner fringes with decreasing
silver halide grain size.
Example 2
Photographic elements according to the invention having backing layers containing
PMMA particles, and resistant to scanner fringes
[0058] Emulsions were prepared, NIR sensitised and coated as in Example 1, but using an
0.18 mm subbed polyester base provided with a backing layer containing 0.3 g/m
2 of poly(methyl methacrylate) particles of mean diameter 0.5 micron in a gelatin binder
(1.3 g/m
2), which was coated from an aqueous solution also containing as in Example I Superamide
L9C and Teepol 610 wetting agents, and formaldehyde hardener. Immediately after coating
onto the film base, the wet backing layer was passed briefly through a chill zone,
at 13°C and 30% relative humidity, causing the gel to set, drying was then brought
about at 30°c and 30% relative humiaity, and appeared to be complete within 1 minute.
The samples were tested in the laser diode scanner system as described above and the
results reported in Table 2.
[0059] The coatings of the same grain size emulsions in Example 1 act as control standards.

Example 3
Photographic elements according to the invention having backing layers containing
non-photosensitive silver halide grains
[0060] An 0.16 micron chlorobromide emulsion was coated as in Example 1, but using a 0.18
mm polyester base provided with a backing layer containing silves halide grains, insensitive
to NIR light, in a gulatin binder (1.3 g/m
2). The effect on scanner fringes of different sizes and loadings of backing grains
is reported in Table 3.

Example 4
Photographic element having backing layer containing other surface roughening agents
[0061] A 0.16 micron chlorobromide emulsion was coated as in Example 1, but on a 0.18 mm
subbed polyester base having a backing containing particles (mean grain size of 0.5
to 2.0 micron) of alkali-soluble methacrylic acid-ethyl methacrylate copolymer, in
a gelatin binder (1.3 g/m
2), which was coated from an aqueous solution containing as in example 1 Superamide
L9C or Teepol 610 wetting agents, and formaldehyde hardener as in Example 1. An otherwise
identical sample was prepared in which the polymer particles were replaced by a lower
loading of silica particles of mean diameter 5 micron. These samples were tested in
comparison with an unbacked one, and the results are reported in Table 4.

[0062] The conventional silica matting, which falls outside the scope of the invention in
particle coverage, gives no protection against fringe formation.
Example 5
Effect of antihalation backing on scanner fringes (0.16 micron chlorobromide emulsion)
[0063] A 0.16 micron chlorobromide emulsion was coated as in Example 1, but on a 0.18 mm
subbed polyester base having a backing consisting of gelatin 5 g/m
2, containing an antihalation dye absorbing strongly between 750 and 900 nm, (Dye 29
in European Patent Application Publication No. 0 101 646) with an optical density
of 0.40 at 820 nm. This was tested in comparison with an unbacked sampled in the laser
diode scanner system, and the results are reported in Table 5.
Example 6
Use of iodobromide emulsions
[0064] A 3% iodobromide emulsion of average grain size 0.21 micron was prepared, chemically
sensitised, stabilised, spectrally sensitised, and coated on transparent 0.18 mm subbed
polyester base, in accordance with Example 17A of European Patent Application Publication
No. 0 088 595. A topcoat of 1.3 g/m
2 of gelatin was simultaneously applied.
[0065] Similar coatings were made on 0.18 mm polyester based having an antihalation backing
consisting of up to three consecutive layers of gelatin (5 g/m
2) containing a dye (Dye 29 in European Patent Application Publication No. 0 101 646),
absorbing strongly between 750 and 900 nm, giving overall optical densities of 0.45,
0.8 and 1.2 at 820 nm. These coatings were tested in the laser diode scanner system,
and the results reportea in Table 5.

[0066] The antihalation layers clearly aid the suppression of fringes.
Example 7
Relation of scanner fringe formation to surface specular reflectivity and surface
roughness
[0067] A 0.16 micron chlorobromide emulsion was coated as in Example 1, but using 0.18 micron
subbed polyester bases provided with backing layers containing a series of concentrations
of PMMA particles of mean diameter 0.5 micron, coated in a gelatin binder (1.3 g/m
2) as in Example 2. These samples were tested in the laser diode scanner system and
the effect on fringe formation is reported in Table 6.

Example 8
Coatings with both dye antihalo and PMMA particle cover
(a) Antihalation Dye and Conventional Matting Agents only
[0068] A chlorobromide emulsion of grain size 0.26 micron was prepared and sensitised using
the methods of Example 1. The emulsion was coated on a 0.18 mm polyester base, at
2.4 g/m
2 silver coverage, simultaneously applying a thin gelatin (1.3 g/m
2) topcoat containing 0.036 g/m
2 of PMMA particles of 2.5 micron mean diameter. The opposite side of the base was
provided with a layer of gelatin (5 g/m
2) containing an infrared absorbing dye (Dye 17 in European Patent Application Publication
No. 0 101 646) giving an infrared absorption from 750 to 900 nm, with an optical density
of 0.6 at 815 nm and having a gelatin topcoat (1.3 g/m
2) containing 0.065 g/m
2 of PM
MA particles of 6 microns mean diameter (backing layer). This coating was tested in
a laser diode scanner and the result is reported in Table 7.
(b) Antihalation Dye and Surface Roughening Agents According to the invention
[0069] The coating in (a) was repeated, with the addition of 0.18 g/m
2 of 0.5 micron PMMA spheres to both the front and the back topcoat layers. The sample
was tested in a laser scanner and the result reported in Table 7.

[0070] Sample (a) was found to give distinctly visible, non-contact scanner fringes whereas
Sample (b) did not give any non-contact scanner fringes under the most stringent conditions
of laser diode scanner testing.
Example 9
Photographic elements having outer matting layers containing particles of an alkali-soluble
copolymer
[0071] A 0.16 micron chlorobromide emulsion was coated as in Example 1, but on a 0.18 mm
polyester base having a backing containing particles of alkali-soluble methacrylic
acid-ethyl methacrylate copolymer, in a gelatin binder (1.3g/m
2), which was coated from an aqueous solution containing Superamide L9C and Teepol
610 wetting agents, and formaldehyde hardener as in Example 1. The copolymer particles
were of mean diameter 0.75 micron but included a broad range of diameters up to 2
micron. Samples containing different densities of this matting agent were tested for
fringe formation in comparison with an unbacked one, and the results are reported
in Table 8.

[0072] The degree to which fringes are suppressed is dependent on the type of construction,
and on the surface density of protruding particles produced by the matting gent. Further
coatings were made in a similar manner using the same 0.16 micron chlorobromide emulsion
and suspensions of copolymer mating agent, but using a 0.18 mm polyester base having
applied to one side an infra-red absorbing antihalation layer, as in Example 5. The
matting layers were applied directly over the antihalation layer, and the photosensitive
emulsion to the opposite side of the film base.
[0073] A third set of coatings has made of the same chlorobromide emulsion on an unbacked
0.18 mm polyester base, as in Example 1, except that the usual emulsion supercoat
was replaced by the matting suspensions of copolymer particles as described above.
[0074] The coatings housing matting backing over an antihalation loayer and those having
matting supercoats to the emulsion were also tested in the laser diode scanner, and
the results represented in Table 8.
1. A photographic element comprising a support transparent to near infrared raaiation,
one or more layers of a silver halide emulsion having grains of an average diameter
of not more than 0.4 micron, sensitised to near infared radiation, characterised in
the element comprises one or more of:
(i) a topcoat layer which is an outermost layer on the same side of the support as
the photosensitive emulsion which topcoat layer is a diffuse transmitting layer with
respect to near infrared radiation,
(ii) a backing layer which is an outermost layer on the side of the support remote
from the photosensitive emulsion which backing layer is a diffuse reflecting layer
or absorbing layer with respect to near infrared radiation,
(iii) a subbing layer which is positioned between the support and the photosensitive
envision which subbing layer is a diffuse transmitting or absorbing layer with respect
to near infrared radiation, whereby the the element may be imaged by a laser scanning
system emitting near infrared radiation substantially without formation of non-contact
interference fringes.
2. A photographic element as claimed in Claim 1, characterised in that the element
comprises a backing layer, comprising a binder containing a surface roughening agent
having average particle size not more than 2 micron, the backing layer having a microscopic
roughness of the outer surface, such that each square millimetre of that surface contains
at least 250,000 particles which protrude above the average level of that surface
by at least 30% of their individual diameters, or by 0.2 micron, whichever is less.
3. A photographic element as claimed in Claim 1, characterised in that the element
comprises a topcoat layer, comprising a binder containing a surface roughening agent
having average particle size not more than 2 micron, this topcoat layer having a microscopic
roughness of tne outer surface, such that each square millimetre of that surface contains
at least 250,000 particles which protrude above the average level of that surface
by at least 30% of their individual diameters, or by 0.2 micron, whichever is less.
4. A photographic element as claimed in Claim 1, characterised in that the microscopic
surface roughness is such that each square millimetre of that surface contains at
least 450,000 particles which protrude above the average level of that surface by
at least 30% of their individual diameters, or by 0.2 micron, whichever is less,
5. A photographic element as claimed in Claim 1, characterised in that the element
comprises a backing or subbing layer containing an antihalation dye absorbing light
in the near infrared and having a peak transmission optical density of at least 0.75,
in that range.
6. A photographic element as claimed in Claim 1, characterised in that the element
comprises a backing layer containing an antihalation dye giving a peak transmission
optical density of at least 0.3 with respect to light in the near infrared, and containing
a surface roughening agent of average particle size not more than 2 micron, this layer
having amicroscopic roughness of the outer surface such that each square millimetre
of that surface contains at least 200,000 particles which protrude above the average
level of that surface by at least 30% of their individual diameters, or by 0.2 micron,
whichever is less.
7. A photographic element as claimed in Claim 1, characterised in that the element
comprises a backing layer having a peak transmission optical density of at least 0.3
with respect to light in the near infrared, and a topcoat layer containing a surface
roughening agent having an average particle size not more than 2 micron, this layer
having a microscopic roughness of the outer surface such that each square millimetre
of that surface contains at least 200,000 particles which protrude above the average
level of that surface by at least 30% of their individual diameters, or by 0.2 micron,
whichever is less.
8. A photographic element as claimed in Claim 1, characterised in that the element
comprises an antihalation subbing layer having a peak transmission optical density
of at least 0.3 with respect to light in the near infrared, and a backing layer or
topcoat layer containing a surface roughening agent having an average particle size
not more than 2 micron, this layer having a microscopic roughness of the outer surface
such that each square millimetre of that surface contains at least 200,000 particles
which protrude above the average level of that surface by at least 30% of their individual
diameters, or by 0.2 micron, whichever is less.
9. A photographic element as claimed in Claim 1, characterised in that the element
comprises a topcoatlayer containing a surface roughening agent having an average particle
size not more than 2 micron, this layer having a microscopic roughness of the outer
surface such that each square millimetre of that surface contains at least 200,000
particles which protrude above the average level of that surface by at least 30% of
their individual diameters, or by 0.2 micron, whichever is less and a backing layer
containing a surface roughening agent having an average particle size not more than
2 micron, this layer having a microscopic roughness of the outer surface such that
each square millimetre of that surface contains at least 200,000 particles which protrude
above the average level of that surface by at least 30% of their individual diameters,
or by 0.2 micron, whichever is less, and optionally a subbing layer containing an
antihalation dye providing a peak transmission optical density of at least 0.3 with
respect to light in the near infrared.
10. A photographic element as claimed in Claim 1, characterised in that the element
comprises a backing and/or topcoat layer comprising a binder containing particles
having a refractive index substantially larger than that of the binder having an average
particle size below 5 micron, the layer(s) being removable during photographic processing.
11. A photographic element as claimed in Claim 10, characterised in that the element
is sensitive to radiation in the wavelength range 750 to 900 nm.
12. A photographic element as claimed in any one of Claims l to 3 and 5 to 9, characterised
in that the particles of roughening agent have an average particle size in the range
0.2 to 2 micron.
13. A photographic element as claimed in anyone of Claims 1 to 3, 5 to 9 and 12, characterised
in that the roughening agent is selected from poly-methyl methacrylate and copolymers
of methacrylic acid with methyl or ethyl methacrylate.
14. A photographic element as claimed in Claim 10, characterised in that the material
of high refractive index has an average particle size in the range 0.2 to 3 micron.
15. A photographic element as claimed in Claim 14, characterised in that the material
of high refractive index is selected from silver halide, zinc oxide and calcium carbonate.
16. A method of recording an image substantially free of non-contact interference
fringes which comprises exposing a photographic element as claimed in any preceding
claim in absence of contact with other surfaces with radiation in the near infrared
from a laser diode scanning system positioned on the emulsion side of the photographic
element and thereafter processing said element to develop the image.