[0001] The present invention relates to color negative photographic recording materials
providing improved performance with reduced silver usage.
[0002] In the art related to light sensitive, multilayer color photographic films, the deleterious
effect of increased layer thickness on image sharpness is well known. This effect
is due to the scattering of light by silver halide grains. Particularly, in multilayer
color photographic materials, the decrease in image sharpness of emulsion layers nearer
to the support is of special concern.
[0003] Previous attempts to improve the sharpness of multilayer color negative photographic
materials by reducing the thickness of the image recording layers have had limited
success. As the amount of silver halide in an imaging layer is reduced, the smaller
number of image-forming centers gives rise to increased granularity. Other important
photographic performance parameters, such as speed, exposure latitude, and high contrast
in separation (spectral color) exposures, can also be compromised by a reduction in
the amount of silver coated in the image-forming layer.
[0004] As the sensitivity (speed) of a multilayer color negative photographic material is
increased, the production of such materials having thin image-forming layers with
low silver coverage, without compromising the other important photographic performance
parameters, becomes more difficult. It is often observed that more sensitive multilayer
color photographic materials have higher silver coverages but are inferior in color
and image quality to less sensitive counterparts. This observation is related to the
practice of obtaining increased emulsion sensitivity by enlarging silver halide grain
size in order to provide a higher probability of the grain absorbing more light.
[0005] This approach to obtaining increased sensitivity is of limited utility due to loss
of photoefficiency with relatively large size silver halide grains. This approach
also requires that in an attempt to maintain the number of imaging centers, and thereby
minimize granularity, the amount of silver used must be increased. The partial grain
development encountered in color negative development worsens this situation as a
large portion of the coated silver halide remains undeveloped and this proportion
becomes greater as the grain volume is increased.
[0006] A very useful approach to increasing light capture of a grain is to alter the grain
morphology. Employment of high aspect ratio tabular silver halide emulsions, as described
in US Patents 4,439,520, 4,672,027, and 4,693,954, has succeeded in providing a large
variety of advantages to color negative photographic recording materials. Such advantages
include improved speed-granularity relationships, increased photographic sensitivity,
higher contrast for a given degree of grain size dispersity, higher separations of
blue and minus blue speeds, less image variance as a function of processing time and/or
temperature variances, the capability of optimizing light transmittance or reflectance
as a function of grain thickness, and reduced susceptibility to background radiation
or airport x-ray radiation damage in very high speed emulsions.
[0007] Silver halide coverages of high speed recording materials that have adequate granularity,
regardless of the silver halide grain morphology, degrade the sharpness of underlying
layers to an undesirable degree. The unrelenting demands for reduced granularity in
high speed films result in the virtually complete use of light incident on the photographic
recording material. Accordingly, silver halide emulsion coverages are, in practice,
increased to the point where further changes do not produce any appreciable net benefit
insofar as granularity is concerned.
[0008] Sharpness loss results in part because the recording material structure thickness
allows geometrical spread of high angle light to substantial lateral distances. Large
grain emulsions are often very turbid at the coating levels necessary to give acceptable
granularity and image density, although such difficulty can be minimized by the use
of high aspect ratio emulsions. Light scattering by overlying layers creates a high
angle light that travels substantial lateral distances in a multilayer photographic
material, causing reduction of the material's resolving power.
[0009] Further disadvantages accrue from both high silver halide coverage and the resultant
substantially diffuse light that is transmitted through the multilayer photographic
material. Increasing the diffuseness of incident light encourages its absorption by
silver halide particles by increasing the light's path length, or residence time,
in the layer. This increased interaction with the silver halide particles provides
some higher off-peak absorption, but may not contribute usefully to photographic speed.
The absorption of off-peak light, which is undesirable since it results in color contamination,
is enhanced to an even greater extent.
[0010] Further, absorption of on-peak light by overlying layers intercepts light desired
to be absorbed in underlying layers, since the incident light is finite in quantity.
Thus, the spectral response of underlying layers can be substantially distorted from
their desirable, normal state by these two processes. The broadened spectral response
produces less accurate color reproduction, and reduced colorfulness of the rendered
image.
[0011] Many of these interdependent problems of multilayer photographic materials would
be ameliorated if thinner, less turbid silver halide emulsion layers could be utilized.
While there are references to reduction in the level of silver or gelatin in a color
photographic silver halide recording material, none of these references provide an
element in which reducing silver coverage is not at the expense of one or more of
speed, density, exposure latitude contrast and/or granularity.
[0012] An early attempt to reduce silver coverage involved using the silver image generated
on development as a catalyst in an amplification process. Such processes are described
in U.S. Patents 3,674,490; 3,748,138 and 3,822,129, and are referred to in U.S. Patent
4,439,520 cited above. The goal of such materials and processes was to reduce the
amount of silver employed in the photographic element. Improvements in photographic
performance parameters, such as granularity and color saturation, were not obtained.
[0013] Attempts to obtain thin silver halide emulsion layers exhibiting improved sensitivity,
and sharpness with reduced graininess, are described in Meyer et al European Patent
Application No. 62202 published October 13, 1982. This application positions a photosensitive
silver halide emulsion layer between color coupler layers which either do not contain
photosensitive silver halide or which contain only silver halide of low sensitivity.
However, overall reduction in silver usage is not realized.
[0014] Japanese Kokai No. 63-226651 seeks color negative photographic materials having improved
sharpness and lowered sensitivity to background radiation through reduced silver usage.
However, density is sacrificed at lower silver coverages.
[0015] U.S. Patent 4,818,667 describes use of photographic recording materials having a
total thickness not greater than 18 »m while preserving image sharpness. However,
this patent does not teach reduction in silver usage while still maintaining desired
density values.
[0016] European Patent Application 311104 published April 12, 1989, describes photographic
recording material having from 3.0 to 9.0 g/m² of silver. However, there is no indication
that satisfactory density values, adequate contrast or reduced granularity values
can be obtained with these materials.
[0017] There remains a need for color negative photographic recording materials having thin
layers and low silver coverage and having improved photographic performance without
sacrificing speed.
Summary of the Invention
[0018] The present inventors have surprisingly found that when certain silver halide emulsions
are used, the coverage of silver halide in an imaging unit can be substantially reduced
below that commonly employed in color negative silver halide photographic elements
without sacrificing image density, contrast and graininess and without the need for
a special amplification process. This permits the preparation of higher speed (ISO
speed ≧ 100) color negative photographic materials that provide performance equal
to or better than currently available color negative materials at the same speed while
at the same time reducing the amount of silver in the element.
[0019] Thus, in one embodiment, this invention provides a color negative photographic recording
material containing a support and at least two silver halide emulsion imaging units
sensitive to different regions of the electromagnetic spectrum, each unit containing
a dye-forming coupler, at least one unit:
(a) comprises from 0.2 to 2.0 g/m², based on silver, of a silver halide emulsion wherein
greater than 50% of the projected area of the grains is provided by tabular grains
having a tabularity of between 50 and 25,000;
(b) has a thickness of less than 4.0 »m;
(c) comprises no more than 2.0 parts by weight of silver per part of coupler; and
(d) capable of yielding a maximum image dye density of at least 2.0 when the recording
material is exposed and processed.
[0020] The color negative photographic recording materials to which this invention relates
typically have an exposure latitude of 2.0 or greater and a contrast (gamma) of 0.9
or less, but that is positive in sign. Exposure latitude and contrast are defined
and measured as described in Strobel et al.,
Photopraphic Materials and Processes, pp. 46-50, Focal Press, Boston, 1986.
[0021] Some color photographic materials intended for reversal processing may have been
described as containing silver levels and silver to coupler ratios within the ranges
described above. However, such reversal materials are not useful as color negative
materials since they would not have the exposure latitude and contrast required.
[0022] The results observed with the present invention contradict the expectation that lowering
the silver halide emulsion coverage and forming a thin layer would result in reduced
image density in the high speed materials of the type to which this invention is directed.
The use of less silver and thinner layers leads to a number of advantages. The sharpness
of photographic images is substantially improved, the transmission of light to underlying
layers is improved, the minus blue to blue speed separation is enhanced, and sensitivity
to higher energy background radiation or X-ray radiation is reduced.
[0023] The use of less silver results in the use of less gelatin, and can result in the
use of less coupler, related solvents and/or dispersing agents. This further contributes
to the thinning of the layer and provides lowered raw material costs. Thinner photographic
layers containing reduced silver levels can lead to an increase in the transmission
of incident light as well as an improvement in the partition of absorbed light among
the spectrally sensitized layers. Moreover, thinner photographic layers containing
reduced silver levels can lead to reduced consumption of processing chemicals, notably
fixing agents, thereby reducing the cost of disposing of these chemicals.
[0024] The tabular grain silver halide emulsions that are useful in the present invention
can be comprised of silver bromide, silver chloride, silver iodide, silver chlorobromide,
silver chloroiodide, silver bromoiodide, silver chlorobromoiodide or mixtures thereof.
These emulsions include (i) high aspect ratio tabular grain emulsions and (ii) thin
intermediate aspect ratio tabular grain silver halide emulsions. High aspect ratio
tabular grain emulsions are those which exhibit an average aspect ratio of greater
than 8:1. Thin, intermediate aspect ratio emulsions are those in which the tabular
grains have an average thickness of less than 0.2 »m and an average aspect ratio ranging
from 5:1 to 8:1. Such emulsions are disclosed by Wilgus et al U.S. Patent 4,434,226,
Daubendiek et al U.S. Patent 4,414,310, Wey U.S. Patent 4,399,215, Solberg et al U.S.
Patent 4,433,048, Mignot U.S. Patent 4,386,156, Evans et al U.S. Patent 4,504,570,
Maskasky U.S. Patent 4,400,463, Wey et al U.S. Patent 4,414,306, Maskasky U.S. Patents
4,435,501 and 4,643,966 and Daubendiek et al U.S. Patents 4,672,027 and 4,693,964.
Also specifically contemplated are those silver bromoiodide grains with a higher molar
proportion of iodide in the core than in the periphery of the grain, such as those
described in GB 1,027,146; JA 54/48,521; US 4,379,837; U.S. 4,444,877; U.S. 4,665,614;
U.S. 4,636,461; EP 264,954; EP 408213 and EP 408214. The silver halide emulsions can
be either monodisperse or polydisperse as precipitated. The grain size distribution
of the emulsions can be controlled by techniques of separation and blending of silver
halide grains of different types and sizes, including tabular grains, as previously
described in the art, for example, in U.S. Patent No. 4,865,964, issued September
12, 1989, entitled BLENDED EMULSIONS EXHIBITING IMPROVED SPEED-GRANULARITY RELATIONSHIPS.
[0025] The high aspect ratio tabular grain emulsions and the thin intermediate aspect ratio
tabular grain emulsions, as well as other emulsions useful in this invention, can
be characterized by a relationship called "tabularity", (T), which is related to aspect
ratio (AR). This relationship can be defined by the following equations:


where ecd is the average equivalent circular diameter of the tabular grains, and t
is the average thickness of the tabular grains, where dimensions are measured in micrometers.
[0026] Tabular grains are those having two substantially parallel crystal faces, each of
which is substantially larger than any other single crystal face of the grain. The
term "substantially parallel" as used herein is intended to include surfaces that
appear parallel on direct or indirect visual inspection at 10,000 X magnification.
[0027] The grain characteristics described above of the silver halide emulsions of this
invention can be readily ascertained by procedures well known to those skilled in
the art. The equivalent circular diameter of the grain is defined as the diameter
of a circle having an area equal to the projected area of the grain as viewed in a
photomicrograph, or an electron micrograph, of an emulsion sample. From shadowed electron
micrographs of emulsion samples it is possible to determine the thickness and the
diameter of each grain as well as the tabular nature of the grain. From these measurements
the average thickness, the average ecd, and the tabularity can be calculated.
[0028] The projected areas of the tabular silver halide grains meeting the tabularity criteria
can be summed. The projected areas of the remaining silver halide grains in the photomicrograph
can be separately summed. From the two sums the percentage of the total projected
area of the silver halide grains provided by the tabular grains meeting the tabularity
criteria can be calculated.
[0029] Good results are obtained when the tabular grain emulsion has a tabularity of from
50 to 25,000;
preferred are elements in which at least one of the emulsions has a tabularity
of from 100 to 5,000; and
especially preferred are elements that employ an emulsion with a tabularity of
from 100 to 2,500.
[0030] As used herein, the term "unit" refers to all of the layers in the element intended
to record radiation in a given region of the spectrum and form a corresponding dye
image. It will be appreciated that each imaging unit can be comprised of one or more
silver halide emulsion layers sensitive to the same region of the spectrum. It is
common with high speed color negative materials of the type to which this invention
relates, for each unit to be composed of 2 or 3 layers, which can be adjacent or not.
At least one of the layers in the unit is, as indicated above, comprised of a silver
halide emulsion in which greater than 50% of the projected area is provided by silver
halide grains having a tabularity of 50 to 25,000. Preferably, if the unit is comprised
of more than one layer, this emulsion is in the most sensitive of the layers, although
other of the layers, or all of the layers, can be comprised of an emulsion with a
tabularity of 50 to 25,000. The emulsion(s) employed in the other layer(s) can be
a non-tabular emulsion or a tabular emulsion that does not satisfy the tabularity
criteria enumerated above so long as the projected area criterion for the unit is
satisfied. If desired, other silver halide emulsions can be blended with the high
tabularity emulsion, so long as the projected area criterion is satisfied.
[0031] The silver halide in these other emulsions can, as with the tabular emulsion, be
comprised of silver bromide, silver chloride, silver iodide, and mixtures of halides
such as silver bromoiodide, silver chlorobromide and silver chlorobromoiodide. Especially
preferred silver halides, for all of the emulsions in the element, are silver bromoiodides.
Preferred proportions of iodide are from 3 to 12 mole percent although lesser or greater
(up to the limit of iodide solubility in bromide) proportions of iodide can be used.
When mixed halides are used in the emulsion grain, the proportions of the halide can
be uniform throughout the grain, or the proportions can vary continuously or discontinuously
across the diameter of the grain, as in core-shell or multiple structure grains.
[0032] The amount of silver halide in the imaging unit of this invention is from 0.2 to
2.0 g/m², based on silver. When the color photographic recording unit has two or more
silver halide layers of different sensitivities to the same region of the visible
spectrum it is preferred that the more sensitive layer comprise from about 0.10 to
about 1.0 g/m² of silver, and the less sensitive layer or layers comprise sufficient
silver to meet the total unit imaging requirement as noted above. Preferably, the
more sensitive layer can comprise from about 0.20 to about 0.6 g/m² of silver.
[0033] One of the features of the photographic recording materials of this invention is
the reduction made possible in silver-to-coupler ratio. For example, conventional
color negative photographic recording materials utilize a substantial excess of silver
as compared to coupler so that a ratio of about 3 parts of silver per part of coupler
is commonplace. Utilization of the instant invention permits use of at least one-third
less silver using the same amount of image coupler. Thus, the silver to coupler ratio
is 2.0 to 1 or less by weight and can go as low as 0.5 to 1 or lower. Preferably,
the element employs a silver to coupler ratio in the range of 0.8:1 to 1.5:1. In determining
silver to coupler ratio all of the compounds that couple with oxidized developing
agents that are in the unit are counted whether or not they contribute to image density.
[0034] Gelatin is commonly used as a vehicle to suspend silver halide grains and prevent
their formation of clumps. Reduction in the amount of silver and the use of lower
silver to coupler ratios than heretofore leads to use of less binder or vehicle.
[0035] With this invention it is possible to reduce gelatin usage by greater than 50%, of
that commonly used while retaining desirable image features and obtaining manufacturing
and ecological advantages. For example, typical cyan and magenta imaging units in
color negative photographic materials contain 2 to 3.3 g/m² of gelatin. With the instant
invention it is also possible to reduce the level of gelatin usage to about 0.5 to
1.5 g/m².
[0036] The improvements made possible by the use of the above described tabular silver halide
grains coupled with reductions in the amounts of silver halide and of gelatin lead
to an appreciably thinner light sensitive recording unit. Thus, color-forming units
of this invention have thicknesses of less than 4.0 »m, with units as thin as 2.0
»m, or less being possible. Preferred color-forming units have thicknesses in the
range of 2.5 to 3.5 »m. In measuring unit thickness only the dye-forming silver halide
layers are included.
[0037] As is typical of color negative materials, the photographic elements of this invention
preferably contain a development inhibitor releasing coupler, especially in the higher
speed layer of a given unit. Typical DIR couplers are described in U.S. Patents 3,148,062;
3,227,554; 3,617,291; 4,095,984; 4,248,962; 4,409,323; 4,477,563; and 4,782,012.
[0038] Inasmuch as improvements in photographic performance become more difficult to achieve
as the speed of the material is increased, the advantages of this invention are particularly
applicable to the higher speed materials, i.e. 100 ISO and greater. The advantages
become especially significant for materials having speeds of 400 to about 6400 ISO.
[0039] The photographic recording materials of this invention are multicolor color elements
that contain dye imaging units sensitive to different regions of the electromagnetic
spectrum. Each unit can be comprised of a single silver halide emulsion layer or of
multiple emulsion layers sensitive to a given region of the spectrum. The layers of
the element, including the layers of the image-forming units, can be arranged in various
orders as is known in the art, for example, from U.S. Patents 4,400,463 and 4,599,302.
[0040] Typically the element comprises imaging units that yield a cyan, magenta and yellow
dye image and the silver halide associated with each unit is sensitized to the complementary
region of the electromagnetic spectrum. However, one or more of the silver halide
layers can be false sensitized to a region of the spectrum that is not the complement
of the dye produced by the coupler with which it is associated. For example, one,
two, or three of the imaging units can be sensitized to different portions of the
infrared region of the spectrum.
[0041] At least one of the imaging units of the element is an imaging unit having the characteristics
defined above. It is preferred that this unit be a magenta dye-forming unit or a cyan
dye forming unit since the visual information provided by each of these units is of
greater significance than that provided by the yellow dye forming unit. In a preferred
embodiment, both of these imaging units have the characteristics described above.
[0042] A typical multicolor photographic recording material comprises a support bearing
a cyan dye image-forming unit comprising at least one red-sensitive silver halide
emulsion layer having associated therewith at least one cyan dye-forming coupler,
a magenta image forming unit comprising at least one green-sensitive silver halide
emulsion layer having associated therewith at least one magenta dye-forming coupler
and a yellow dye image-forming unit comprising at least one blue-sensitive silver
halide emulsion layer having associated therewith at least one yellow dye-forming
coupler. In addition to the coupler that forms a dye complementary to the sensitization
of the associated silver halide emulsion, the layer can contain one or more non-complementary
couplers in order to modify perceived photographic performance. The recording material
is coated on a support and can contain additional layers, such as filter layers, image
modifier layers, interlayers, overcoat layers, subbing layers, and the like.
[0043] The maximum image density of at least 2.0 is obtained by processing the element in
the way it is intended to be used. Image density refers to the density range between
Dmin and Dmax of the exposed and processed element. This would be one of the common
color negative processes used to develop color negative amateur and motion picture
films such as the ECN-2 or C-41 process. A typical process is described in the 1988
Annual of the British Journal of Photography pages 196-198, and is as follows:
(1). develop for 3 minutes, 15 seconds at 37.8°C in a solution comprising:

pH @ 26°C 10.0 +/- 0.05
(2). bleach for 4 minutes at a temperature of 37.8°C in a solution comprising:

(3). wash with water for 3 minutes at 35-36°C;
(4). fix for 4 minutes at a temperature of 37.8°C in a solution comprising:

pH of 6.5 ± 0.15;
(5). wash with water for 3 minutes at 35-36°C; and
(6). stabilize for 1 minute at 37.8°C in a solution comprising:

[0044] In the following discussion of suitable materials for use in the recording materials
of this invention, reference will be made to
Research Disclosure, December 1978, Item 17643, published by Kenneth Mason Publications, Ltd., Dudley
Annex, 12a North Street Emsworth Hampshire PO10 7DQ, ENGLAND, the disclosures of which
are incorporated herein by reference. This publication will be identified hereafter
by the term "
Research Disclosure".
[0045] Sensitizing compounds, such as compounds of copper, thallium, lead, bismuth, cadmium,
selenium, iridium and other Group VIII noble metals, can be present during precipitation
of the silver halide emulsions.
[0046] The silver halide emulsions can be chemically sensitized. Noble metal (e.g., gold),
middle chalcogen (e.g., sulfur, selenium, or tellurium), and reduction sensitizers,
employed individually or in combination, are specifically contemplated. Typical chemical
sensitizers are listed in
Research Disclosure, Item 17643, cited above, Section III. The chemical sensitization can be accomplished
in the presence of finish modifiers such as those described in U.S. Patent 4,578,348.
[0047] The silver halide.emulsions can be spectrally sensitized with dyes from a variety
of classes, including the polymethine dye class, which includes the cyanines, merocyanines,
complex cyanines and merocyanines (i.e., tri-, tetra-, and poly-nuclear cyanines and
merocyanines), oxonols, hemioxonols, styryls, merostyryls, and streptocyanines. Illustrative
spectral sensitizing dyes are disclosed in
Research Disclosure, Item 17643, cited above, Section IV.
[0048] Suitable vehicles for the emulsion layers and other layers of elements of this invention
are described in Research Disclosure Item 17643, Section IX and the publications cited
therein.
[0049] Couplers useful in this invention can be polymeric or nonpolymeric. Typical cyan
dye forming couplers that are useful in this invention are phenols and naphthols.
Typical magenta dye forming couplers are pyrazolones and pyrazoloazoles. Typical yellow
dye forming couplers are acetoacetanilides and benzoylacetanilides. Such dye image-forming
couplers, which can be of the one, two or four equivalent type and can be coated in
or adjacent to silver halide emulsion layers to be free to react with oxidized developing
agent to form the desired image. Minor amounts of couplers which form different colored
images may be incorporated within the dye forming units of the present invention.
For example, the addition of a small amount of a cyan coupler to a magenta dye forming
layer will alter the hue of the resulting magenta image. In addition, the imaging
unit can contain image modifying couplers and compounds which release development
inhibitor moieties, development accelerator moieties or bleach accelerating moieties.
These moieties are released from such compounds, or from a timing group contained
within such compounds, as the result of processing.
[0050] The photographic recording materials of this invention can contain brighteners (Research
Disclosure Section V), antifoggants and stabilizers (Research Disclosure Section VI),
antistain agents and image dye stabilizers (Research Disclosure Section VII, paragraphs
I and J), light absorbing and scattering materials (Research disclosure Section VIII),
hardeners (Research Disclosure Section XI), plasticizers and lubricants (Research
Disclosure Section XII), matting agents (Research Disclosure Section XVI) and development
modifiers (Research Disclosure Section XXI). The photographic materials can have incorporated
therein developing agents to render them suitable for activation processing as described
in U.S. Patent 3,342,599.
[0051] The photographic recording materials can be coated on a variety of supports as described
in Research Disclosure Section XVII and the references described therein.
[0052] Photographic recording materials can be exposed to actinic radiation, typically in
the visible region of the spectrum, to form a latent image as described in Research
Disclosure Section XVIII and then processed to form a visible dye image as described
in Research Disclosure Section XIX. Processing to form a visible dye image includes
the step of contacting the element with a color developing agent to reduce developable
silver halide and oxidize the color developing agent. Oxidized color developing agent
in turn reacts with the coupler to yield a dye.
[0053] The following examples further illustrate this invention.
[0054] A series of color negative, incorporated coupler photographic materials were prepared
by coating the following layers in order, on a cellulose triacetate film support.
The physical properties of the emulsions utilized, the unit silver coverages, silver
to coupler ratio, and unit thickness of the magenta units are described in Tables
I and II which follow the description of the preparation of the photographic materials.
[0055] A first photographic recording material of the invention was prepared by coating
the following layers, in order, on a cellulose triacetate film support bearing a layer
of black colloidal silver sol at 0.30 g/m² and gelatin at 2.44 g/m². The material
was designated Element I.
Element I (Invention)
[0056]
- Layer 1
- Slow Cyan Layer - comprising red-sensitized tabular silver bromoiodide grains (3.9
mole % I⁻) at 0.70 gAg/m², gelatin at 1.61 g/m², cyan image-forming coupler A at 0.54
g/m², DIR coupler B at 0.0043 g/m², masking coupler C at 0.068 g/m², and antifoggant
4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene at 0.012 g/m².
- Layer 2
- Fast Cyan Layer - comprising faster red-sensitized tabular silver bromoiodide grains
(4.0 mole % I⁻) at 0.65 gAg/m², gelatin at 1.15 g/m², cyan image-forming coupler D
at 0.29 g/m², masking coupler C at 0.029 g/m², and antifoggant 4-hydroxy-6-methyl-
1,3,3a,7-tetraazaindene at 0.011 g/m².
- Layer 3
- Interlayer - comprising gelatin at 0.65 g/m² and oxidized developer scavenger didodecylhydroquinone
at 0.054 g/m².
- Layer 4
- Slow Magenta Layer - comprising green-sensitized tabular silver bromoiodide grains
(2.4 mole % I⁻) at 0.52 gAg/m², gelatin at 1.16 g/m², image-forming couplers E at
0.30 g/m² and F at 0.13 g/m², DIR coupler B at 0.027 g/m², masking coupler G at 0.069
g/m², and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene at 0.008 g/m².
- Layer 5
- Fast Magenta Layer - comprising faster green-sensitized tabular silver bromoiodide
grains (4.0 mole % I⁻) at 0.39 gAg/m², gelatin at 0.60 g/m², image-forming couplers
E at 0.075 g/m² and F at 0.032 g/m², DIR coupler H at 0.006 g/m², masking coupler
G at 0.017 g/m², and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene at 0.006
g/m².
- Layer 6
- Yellow Filter Layer - comprising gelatin at 0.65 g/m², Carey Lea silver at 0.022 g/m²,
and oxidized developer scavenger didodecylhydroquinone at 0.054 g/m².
- Layer 7
- Slow Yellow Layer - comprising blue-sensitized tabular silver bromoiodide grains (4.2
mole % I⁻) at 0.32 gAg/m², gelatin at 1.61 g/m², image-forming coupler I at 1.08 g/m²,
DIR coupler J at 0.065 g/m², and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
at 0.008 g/m².
- Layer 8
- Fast Yellow Layer - comprising faster blue-sensitized tabular silver bromoiodide grains
(3.0 mole % I⁻) at 0.59 gAg/m², gelatin at 1.20 g/m², image-forming coupler I at 0.43
g/m², DIR coupler J at 0.032 g/m², and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
at 0.009 g/m².
- Layer 9
- Protective Overcoat and UV Filter Layer - comprising gelatin at 1.22 g/m², silver
bromide Lippmann emulsion at 0.11 g/m², UV absorbers at 0.23 g/m², and bis(vinylsulfonyl)methane
added at 2.0% of total gelatin weight.
Element II (Invention)
[0057] A second photographic recording material of the invention, designated Element II,
was prepared in a similar manner to Element I. The following modifications were made
in the magenta dye forming unit.
- Layer 4
- Slow Magenta Layer - DIR Coupler B was reduced to 0.019 g/m².
- Layer 5
- Fast Magenta Layer - the coverage of the faster green-sensitized tabular silver bromoiodide
grains was increased to 0.65 gAg/m², gelatin increased to 0.97 g/m² and DIR coupler
H was 0.011 g/m².
[0058] A third color photographic recording material of the invention, designated Element
III, for color negative development was prepared by applying the following layers
in the given sequence to a transparent support of cellulose triacetate. All silver
halide emulsions were stabilized with 2 grams of 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
per mole of silver.
Element III (Invention)
[0059]
Layer 1 (Antihalation Layer) Black colloidal silver sol containing 0.236 g/m² of silver and 2.44 g/m² gelatin.
Layer 2 Slow Cyan Layer - Comprising red-sensitized silver iodobromide emulsion (4
mol % I⁻) at 0.194 g/m², red-sensitized silver iodobromide emulsion (4 mol % I⁻) at
0.280 g/m², cyan dye-forming image coupler D at 0.463 g/m², DIR compound B at 0.032
g/m², BAR compound N at 0.020 g/m², with gelatin at 1.053 g/m².
Layer 3 Fast Cyan Layer - Comprising red-sensitized silver iodobromide emulsion (4.1
mol % I⁻) at 0.495 g/m², cyan dye-forming image coupler D at 0.183 g/m², DIR compound
B at 0.019 g/m², BAR compound N at 0.016 g/m², with gelatin at 0.720 g/m².
Layer 4 (Interlayer) Comprising oxidized developer scavenger didodecylhydroquinone at 0.054 g/m², dye
MD-1 at 0.107 g/m², and dye YD-1 0.150 g/m² with 0.645 g/m² of gelatin.
Layer 5 Slow Magenta Layer - Comprising green-sensitized silver iodobromide emulsion
(2.6 mol % I⁻)at 0.204 g/m², green-sensitized silver iodobromide emulsion (3 mol %
I⁻ at 0.065 g/m², magenta dye-forming image coupler E at 0.151 g/m², magenta dye-forming
image coupler F at 0.194 g/m², DIR compound B at 0.012 g/m² with gelatin at 0.613
g/m².
Layer 6 Fast Magenta Layer - Comprising green-sensitized silver iodobromide emulsion
(4 mol % I⁻) at 0.430 g/m², magenta dye-forming image coupler E at 0.0425, magenta
dye-forming image coupler F at 0.043 g/m², DIR compound H at 0.0097 g/m² with gelatin
at 0.527 g/m².
Layer 7 (Interlayer) Comprising oxidized developer scavenger didodecylhydroquinone at 0.54 g/m², yellow
colloidal silver at 0.022 g/m² with 0.645 g/m² of gelatin.
Layer 8 Slow Layer - Comprising blue-sensitized silver iodobromide emulsion (4 mol
% I⁻ ) at 0.322 g/m², yellow dye-forming image coupler I at 0.613 g/m², DIR compound
J at 0.0194 g/m², 2-propargylamino-benzoxazole at 0.043 mg/m² with gelatin at 0.914
g/m².
Layer 9 Fast Yellow Layer - Comprising blue-sensitized silver iodobromide emulsion
(3 mole % I⁻) at 0.409 g/m², yellow dye-forming image coupler I at 0.226 g/m², DIR
compound J at 0.0097 g/m², 2-propargylamino-benzoxazole at 0.043 mg/m² with gelatin
at 0.645 g/m².
Layer 10 (Protective Layer 1) 0.967 g/m² of gelatin, 0.108 g/m² of dye UV-1, 0.118 g/m² of dye UV-2.
Layer 11 (Protective Layer 2) Unsensitized silver bromide Lippman emulsion at 0.108 g/m², anti-matte polymethylmethacrylate
beads at 0.025 g/m², gelatin at 0.54 g/m² with 2% by weight to total gelatin of hardener
H-1.
[0060] A comparative control color negative photographic recording material designated Element
IV, that is known to produce ISO 400 speed, was coated in an analogous fashion on
a cellulose triacetate support bearing an antihalation layer in the layer order recited:
- Layer 1
- Slow Cyan Layer - comprising a blend of three red-sensitized silver bromoiodide grains,
a medium size tabular grain emulsion (6.0 mole % I⁻) at 0.91 gAg/m², a smaller tabular
grain emulsion (3.0 mole % I⁻) at 0.28 gAg/m² and a non-tabular grain emulsion (4.8
mole % I⁻) at 0.97 gAg/m², gelatin at 2.59 g/m², cyan image-forming coupler A at 0.72
g/m², DIR coupler K at 0.044 g/m², masking coupler C at 0.054 g/m², bleach accelerator
releasing coupler N at 0.075 g/m², and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
at 0.071 g/m².
- Layer 2
- Fast Cyan Layer - comprising faster red-sensitized tabular silver bromoiodide grains
(6.0 mole % I⁻) at 1.29 gAg/m², gelatin at 1.73 g/m², cyan image-forming coupler D
at 0.23 g/m², DIR coupler K at 0.043 g/m², masking coupler C at 0.043 g/m² and antifoggant
4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene at 0.043 g/m².
- Layer 3
- Interlayer - comprising gelatin at 1.29 g/m² and dye YD-1 at 0.031 g/m².
- Layer 4
- Slow Magenta Layer - comprising a blend of green-sensitized silver bromoiodide grains,
tabular silver bromoiodide grains (3.0 mole % I⁻) at 0.38 gAg/m², non-tabular silver
bromoiodide grains (4.8 mole % I⁻) at 0.81 g/m², gelatin at 2.15 g/m², image- forming
coupler F at 0.59 g/m², DIR coupler H at 0.011 g/m², masking coupler G at 0.059 g/m²,
and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene at 0.019 g/m².
- Layer 5
- Fast Magenta Layer - comprising faster green-sensitized tabular silver bromoiodide
grains (6.0 mole % I⁻) at 1.23 gAg/m², gelatin at 1.80 g/m², image-forming coupler
F at 0.17 g/m2, DIR coupler H at 0.011 g/m², masking coupler G at 0.028 g/m², and
antifoggant 4-hydroxy-5-methyl-1,3,3a,7-tetraazaindene at 0.015 g/m².
- Layer 6
- Yellow Filter Layer - comprising gelatin at 1.29 g/m², and Cary Lea silver at 0.022
g/m².
- Layer 7
- Slow Yellow Layer - comprising blue-sensitized tabular silver bromoiodide grains (6.0
mole % I⁻) grains at 0.75 gAg/m², gelatin at 2.27 g/m², image-forming coupler L at
1.58 g/m², DIR coupler M at 0.083 g/m², antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
at 0.012 g/m².
- Layer 8
- Fast Yellow Layer - comprising faster blue-sensitized low aspect ratio silver bromoiodide
grains (9.0 mole % I⁻) at 0.74 g/m², gelatin at 1.60 g/m², image-forming coupler L
at 0.23 g/m², and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene at 0.012
g/m².
- Layer 9
- Protective Overcoat and UV Filter Layer - comprising gelatin at 1.15 g/m², silver
bromide Lippmann emulsion at 0.22 gAg/m² and bis(vinylsulfonyl)methane added at 2.0%
of total gelatin weight.

[0061] The above described photographic elements were evaluated to determine photographic
performance as reported in Table III. In one evaluation, each element was exposed
for 1/100 of a second to a 600W, 3000°K tungsten light source that was filtered by
a Daylight Va filter to 5500°K through a graduated 0-4.0 density step tablet to determine
minimum density and gamma. In another evaluation each element was exposed as the first,
except that the exposure time was 0.2 second, to allow determination of the maximum
density. In another evaluation, each element was exposed at 0.2 second and a green
Wratten 99 filter was added in order to assess the separation exposure gamma and maximum
density. To determine the rms granularity, by the method described in H.C. Schmitt,
Jr. and J. H. Altman, Applied Optics 9, pp. 871-874, April 1970, each element was
exposed as in the first evaluation, except the filter pack contained a 0.6 neutral
density and the 0-4.0 density step tablet was replaced by a 0-3.0 density step tablet
and matte glass diffuser.
[0062] The sharpness measurements were made by determining the Modulation Transfer Function
(MTF) by the procedure described in
Journal of Applied Photographic Engineering, 6 (1):1-8, 1980. Modulation Transfer Functions for red light were obtained by exposing
each element for 1/15 second at 60% modulation using 70 B and 20 C KODAK Color Compensating
Filters, and a 0.2 neutral density filter.
[0063] The exposed samples were developed for 3.25 minutes in the 6-step development process
described above on pages 16 and 17. The processed film strips were then evaluated
for speed, contrast, net maximum density (Dmax minus Dmin) for both white light and
green light exposures and granularity for the magenta color-forming unit. The 35 mm
System Cascaded Modulation Transfer (AMT) Acutance Ratings are reported in Table III
for the cyan color-forming unit. The results are shown in Table III.

The construction of a thin color magenta color forming unit containing tabular grain
silver halide emulsions of the preferred grain tabularity according to the present
invention is shown to provide improved sharpness in underlying emulsion layers while
improving or maintaining sensitivity, contrast, maximum density and granularity at
substantially exposure latitude, reduced silver coverage.
Structures
[0065] As further illustration of the ability of high tabularity emulsions, coated in thin
layers and at low silver to coupler ratios, to produce a maximum image dye density
of at least 2.0, a series of twenty bicolor incorporated coupler photographic coatings
were prepared. The series was composed of five different silver bromoiodide (4.0 mole
% I) emulsions of varying physical properties (three within and two outside the invention)
having approximately the same surface area per grain to obtain equal spectrally sensitized
speed. Each of the five emulsions was coated in four separate element types which
differed in the amount of material in the magenta unit. Three provided elements having
unit silver, silver/coupler ratio, and thickness values of the invention and the fourth
serves as a control. The materials were prepared by coating the following layers in
order, on a cellulose triacetate film support having an antihalation layer on the
opposite side.
Element A (Invention)
[0066]
- Layer 1
- Cyan Layer - comprising a blend of three red-sensitized silver bromoiodide grains,
a medium size tabular grain emulsion (6.0 mole % I⁻) at 0.91 gAg/m², a smaller tabular
grain emulsion (3.0 mole % I⁻) at 0.28 gAg/m² and a non-tabular grain emulsion (4.8
mole % I⁻) at 0.97 gAg/m², gelatin at 2.59 g/m², cyan image forming coupler A at 0.72
g/m², DIR coupler K at 0.044 g/m², masking coupler C at 0.054 g/m², bleach accelerator
releasing coupler N at 0.075 g/m², and antifoggant 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
at 0.071 g/m².
- Layer 2
- Interlayer - comprising gelatin at 1.29 g/m².
- Layer 3
- Magenta Layer - comprising one of the five green-sensitizing silver bromoiodide emulsions
(4.0 mole % I⁻) described in Table I at 0.49 gAg/m², gelatin at 1.30 g/m², and image
forming coupler E at 0.49 g/m².
- Layer 4
- Protective Overcoat - comprising gelatin at 1.08 g/m² with 2.0% by weight to total
gelatin of hardener H-1.
Element B (Invention)
[0067] A second photographic recording material, designated Element B, was prepared in a
similar manner to Element A with the following modifications to the Magenta dye forming
unit.
- Layer 3
- Magenta Layer - green-sensitized silver bromoiodide emulsion was increased to 0.72
gAg/m². Gelatin was increased to 1.86 g/m², and image forming coupler E was increased
to 0.72 gAg/m².
Element C (Invention)
[0068] A third photographic recording material, designated Element C, was prepared in a
similar manner to Element A with the following modifications to the Magenta dye forming
unit.
- Layer 3
- Magenta Layer - green-sensitized silver bromoiodide emulsion was increased to 1.00
gAg/m². Gelatin was increased to 1.95 g/m².
Element D (Control)
[0069] A fourth photographic recording material, designated Element D, was prepared in a
similar manner to Element A with the following modifications to the Magenta dye forming
unit.
- Layer 3
- Magenta Layer - green-sensitized silver bromoiodide emulsion was increased to 1.73
gAg/m². Gelatin was increased to 2.91 g/m².
[0070] The photographic elements were exposed for 1/10 of a second to a 600W, 3000°K tungsten
light source that was filtered by a Daylight Va filter to 5500°K and a green Wratten
99 filter through a graduated 0-4.0 density step tablet, and they were processed for
3.25 minutes under the conditions described above. The film strips were then evaluated
for net maximum density (Dmax-Dmin).
1. Photographisches Farbnegativ-Aufzeichnungsmaterial mit einem Träger und mindestens
zwei bildaufzeichnenden Silberhalogenidemulsionseinheiten, die gegenüber verschiedenen
Bereichen des elektromagnetischen Spektrums empfindlich sind, wobei jede Einheit einen
einen Farbstoff bildenden Kuppler enthält, und wobei mindestens eine Einheit eine
hoch tafelförmige Einheit ist, die:
a) 0,2 bis 2,0 g/m², bezogen auf Silber, einer Silberhalogenidemulsion aufweist, in
der mehr als 50 % der projizierten Fläche der Körner von tafelförmigen Körnern stammen,
die eine Tafelförmigkeit zwischen 50 und 25000 aufweisen;
b) eine Dicke von weniger als 4,0 »m aufweist;
c) nicht mehr als 2,0 Gewichtsteile Silber pro Gewichtsteil Kuppler aufweist; und
d) zu einer maximalen Bildfarbstoffdichte von mindestens 2,0 führt, wenn das Aufzeichnungsmaterial
exponiert und entwickelt wird.
2. Aufzeichnungsmaterial nach Anspruch 1, in dem die tafelförmigen Körner eine Tafelförmigkeit
zwischen 100 und 5000 aufweisen.
3. Aufzeichnungsmaterial nach Anspruch 1, in dem die tafelförmigen Körner eine Tafelförmigkeit
zwischen 100 und 2500 aufweisen.
4. Aufzeichnungsmaterial nach Anspruch 1, in dem die Einheit der hohen Tafelförmigkeit
mindestens zwei Silberhalogenidemulsionsschichten umfaßt mit verschiedenen Empfindlichkeiten
gegenüber dem gleichen Bereich des Spektrums.
5. Aufzeichnungsmaterial nach Anspruch 4, in dem die empfindlichere Schicht 0,10 bis
1,0 g/m² Silber enthält.
6. Aufzeichnungsmaterial nach Anspruch 4, in dem die empfindlichere Schicht 0,20 bis
0,6 g/m² Silber enthält.
7. Aufzeichnungsmaterial nach Anspruch 1, in dem in der Einheit hoher Tafelförmigkeit
0,8 bis 1,5 Teile Silber pro Teil Kuppler vorliegen.
8. Aufzeichnungsmaterial nach Anspruch 1, in dem in der Einheit hoher Tafelförmigkeit
0,5 bis 1 Teil Silber pro Teil Kuppler vorliegen.
9. Aufzeichnungsmaterial nach Anspruch 1, in dem die Einheitendicke der Einheit von hoher
Tafelförmigkeit bei 2,5 bis 3,5 »m liegt.
10. Aufzeichnungsmaterial nach Anspruch 1, das mindestens 3 Silberhalogenid-Bildaufzeichnungseinheiten
umfaßt, die gegenüber verschiedenen Bereichen des Spektrums empfindlich sind.
11. Aufzeichnungsmaterial nach Anspruch 1, in dem die tafelförmigen Körner mindestens
eines der Silberhalogenide Silberbromid oder Silberbromoiodid aufweisen.
12. Aufzeichnungsmaterial nach Anspruch 1, in dem die Einheit hoher Tafelförmigkeit eine
einen blaugrünen Farbstoff liefernde Einheit oder eine einen purpurroten Farbstoff
liefernde Einheit ist.
13. Aufzeichnungsmaterial nach Anspruch 1, in dem mindestens eine der Einheiten einen
einen Entwicklungsinhibitor freisetzenden Kuppler enthält.
14. Aufzeichnungsmaterial nach Anspruch 1, in dem die Einheit hoher Tafelförmigkeit einen
einen Entwicklungsinhibitor freisetzenden Kuppler enthält.