Field of the Invention
[0001] This invention relates to a process for producing a silver halide photographic emulsion
comprising regularly shaped silver halide grains.
Background of the Invention
[0002] Silver halide emulsions used in silver halide photographic materials are usually
subjected to chemical sensitization using a sulfur sensitizer, a selenium sensitizer,
a reduction sensitizer, a noble metal sensitizer, either alone or in combination,
for the purpose of obtaining a desired sensitivity and gradation. Among others, sulfur
sensitizers, selenium sensitizers and noble metal sensitizers are important.
[0003] Further, for the purpose of attaining excellent color reproduction, silver halide
emulsions are spectrally sensitized with sensitizing dyes so as to exhibit sensitivity
to light of longer wavelengths to which silver halides are by nature substantially
insensitive.
[0004] With the recent demand for increasing sensitivity of silver halide emulsions, particularly
in the wavelength region for which spectral sensitization is performed, it has been
attempted to increase the amount of the sensitizing dye to be added to the silver
halide emulsion to increase the light absorption.
[0005] A spectral sensitization sensitivity Sλ (at a wavelength λ) obtained by addition
of a sensitizing dye can be determined according to the equation:
wherein S°400 and S400 represent the photographic sensitivity of the spectrally non-sensitized
emulsion and that of the spectrally sensitized emulsion, respectively, at a wavelength
of 400 nm; φ
r represents a relative quantum efficiency; and Aλ and A400 represent percent absorption
at a wavelength of λ and 400 nm, respectively.
[0006] Addition of a large quantity of sensitizing dyes is favorable for increasing absorption
but, at the same time, causes reduction of φ
r or reduction of S400/S°400 (generally called "desensitization of intrinsic sensitivity"),
which ultimately results in reduction of photographic sensitivity.
[0007] Although various supersensitization techniques have been developed for improving
φ
r or preventing desensitization, the inefficiency resulting from an approach of a saturated
adsorption on silver halide grains cannot be sufficiently suppressed by these techniques.
[0008] Simson et al. report that inherent desensitization does not occur when a sensitizing
dye is adsorbed onto the surface of internal latent image type emulsion grains whose
core has been chemically sensitized, as described in J.W. Simson & W.S. Gavgh,
Photographic Science Engineering, Vol. 19, 339 (1975). However, since the emulsion of this type exhibits internal
sensitivity, no image appears when developed with a surface developer. Besides, a
color developer used for color photographic materials is not applicable to the internal
latent image type emulsion because of its low solubility. All the other conventional
developers have insufficient solubility to be applied to the internal latent image
type emulsion.
[0009] It has also been proposed to use a shallow internal latent image type emulsion which
forms a latent image in a very shallow portion beneath the grain surface. However,
if silver halide grains have a suitable shell thickness to be developed with a developer
having ordinary solubility, desensitization would be likely or development would be
considerably retarded.
[0010] A chemical sensitization technique is desired which provides a high sensitivity silver
halide emulsion without causing reduction of inherent sensitivity due to a dye, as
is encountered in using a developer having low solubility.
[0011] If chemical sensitization nuclei, i.e., positions where a latent image is to be formed,
can be formed on the surface of silver halide grains, unlike the method of Simson
et al., apart from most of adsorbed dye particles, the reduction of inherent sensitivity
due to the dye should be suppressed even when the silver halide is developed with
a general developer of low solubility. The conventional techniques, including the
method of Simson et al., rarely have referred to possibility of isolating latent image
specks from an adsorbed dye as well as controllability of the position of the chemical
sensitization nuclei where a latent image is to be formed. However, intentional formation
of chemical sensitization nuclei at a limited position of the surface of silver halide
grains without scatter would favor a silver halide emulsion with increased sensitivity.
Accordingly, it has been keenly demanded to develop a method for highly controlling
the position of chemical sensitization nuclei, and to produce a high sensitivity silver
halide emulsion obtained thereby.
[0012] There are some reports with respect to addition of dyes, such as methine dyes, to
a silver halide emulsion during chemical sensitization.
[0013] Further, several cases have been known where a sensitizing dye is added to a silver
halide emulsion at the beginning of chemical sensitization as described, e.g., in
US-A-4,435,501 and JP-A-62-141112. However, these cases concern silver halide twins
(tabular grains). JP-A-61-133941, JP-A-59-9153, JP-A-58-28738 and JP-A-62-7040 also
refer to the addition of a sensitizing dye at the time of chemical sensitization.
(The term "JP-A" as used herein refers to a "published unexamined Japanese patent
application".)
[0014] Furthermore, JP-A-61-311131 describes control of positions of development centers,
i.e., positions of chemical sensitization, and particularly formation of development
centers, i.e., chemical sensitization nuclei, on a (111) plane. Moreover, the dye
is employed without being accurately evaluated for its adsorption selectivity, and
halogen conversion is chiefly used here.
[0015] JP-A-62-152330 teaches the use of a compound called a "CR compound" in order to form
a development center on the top of octahedral or tetradecahedral normal crystals having
a (111) plane, that is, on a plane other than the (111) plane.
[0016] In addition, it is also known to add a dye at the time of grain formation preceding
chemical sensitization as disclosed, e.g., in US-A-2,735,766, 3,628,960, 4,183,756
and 4,225,666, JP-A-60-196749, JP-A-61-103149 and JP-A-61-165751, and
Research Disclosure, No. 19227, Vol. 192, 155 (1980). In most of these cases, the dye added exists in
the system during the subsequent chemical sensitization.
[0017] Some chemical sensitizers which selectively sensitize a (100) plane instead of a
(111) plane, and particularly sulfur sensitizers, are known in the art, as described
in
Research Disclosure, Nos. 17643 and 18716,
J. Phys. Chem., Vol. 57, 725 (1953), US-A-2,278,947 and 2,410,689, and JP-B-58-28568 (the term "JP-B"
as used herein refers to an "examined Japanese patent publication").
[0018] Selective chemical sensitization is referred to in
Journal of Photographic Science, Vol. 23, 249 (1975), describing that sodium thiosulfate chemically sensitizes a
(111) plane selectively.
[0019] EP-A-0 097 790 discloses the preparation of octahedral or tetradecahedral silver
bromoiodide grains whose surface area is bounded by (111) crystal faces to at least
5 %, whereby the grains are chemically gold/sulphur sensitized in the presence of
a nitrogen-containing silver complexing compound.
Summary of the Invention
[0020] Object of this invention is to provide a process for preparing a high sensitivity
silver halide emulsion, which includes chemical sensitization and spectral sensitization
under control.
[0021] It has now been found that the object of the invention can be accomplished by a process
for producing a silver halide photographic emulsion comprising regularly shaped silver
halide grains comprising a (111) face and a (100) face comprising adding a spectral
sensitizing dye capable of selectively adsorbing onto the (111) face of the grains
to the emulsion, and then subjecting the emulsion to chemical sensitization using
at least one sulfur compound to preferentially form chemically sensitized nuclei on
the (100) face of the grains, whereby the dye is used in an amount greater than that
required for entirely covering the (111) face and whereby 60% or more of fine silver
specks formed by development are formed on the (100) face.
[0022] The invention further provides a process for producing a silver halide photographic
emulsion comprising regularly shaped silver halide grains comprising a (111) face
and a (100) face, comprising the steps of
(a) adding a spectral sensitizing dye capable of selectively adsorbing to a greater
extent on the (111) face than on the (100) face,
(b) subjecting said emulsion to chemical sensitization using a sulfur compound selected
from thioureas, rhodanines, oxazolidines or polysulfides, and
such that chemically sensitized nuclei are preferentially formed on the (100) face
of the grains, wherein
(i) the (111) face occupies at least 40% of the surface of the grains or the (100)
face occupies more than 60% of the surface of the grains and wherein
(ii) said adding step (b) is carried out during or after said subjecting step (a).
BRIEF DESCRIPTION OF THE DRAWINGS
[0023] Figures 1 and 2 are electron micrographs (magnification: × 15,600) of silver halide
crystal grains in Samples 1 and 2 prepared in Example 1, respectively.
DETAILED DESCRIPTION OF THE INVENTION
[0024] The normal silver halide grains contained in the silver halide emulsion layer produced
by the process of the present invention are crystals having substantially no stacking
fault of twin plane. The silver halide grains have both (111) plane and (100) plane
on which a latent image is preferentially formed, and the grains may have a high index
of (h, k, ℓ) plane such as (331) plane, (210) plane, (321) plane and (211) plane.
The normal silver halide grains generally have an average grain size of from 0.1 to
6 µm, preferably from 0.1 to 4 µm, more preferably from 0.2 to 3 µm, and the grains
are generally contained in an amount of at least 50%, preferably 60% or more, particularly
preferably 75% or more, based on the total projected area of silver halide grains
contained in the silver halide emulsion layer.
[0025] When the (111) plane occupies at least 40% of the surface of the silver halide grains
having a (111) plane and a (100) plane, the grains are spectrally sensitized with
a spectral sensitizing dye selectively adsorbed more on one plane than on the other
plane, generally the amount of the dye adsorbed on the one surface being least 60%,
preferably 70% or more and particularly preferably 75% or more, based on the total
amount of the dye adsorbed on both planes.
[0026] Typical embodiments of light-sensitive materials include:
(I) A silver halide photographic material comprising a support having thereon at least
one silver halide emulsion layer containing at least 50%, based on the total projected
area of silver halide grains, of substantially normal silver halide grains mainly
composed of a (111) plane and a (100) plane, wherein the (111) plane occupies at least
40% of the surface of the normal grains, at least 60% of the number of the normal
grains being spectrally sensitized with at least one sensitizing dye selectively adsorbed
more on the (111) plane than on the (100) plane, and being capable of preferentially
forming a latent image on the (100) plane.
(II) A silver halide photographic material comprising a support having thereon at
least one silver halide emulsion layer containing substantially normal silver halide
grains having a (111) plane and a (100) plane, wherein the (111) plane occupies at
least 40% of the surface of the grains, the normal grains being spectrally sensitized
with at least one sensitizing dye selectively adsorbed more on the (100) plane than
on the (111) plane and being capable of preferentially forming a latent image on the
(100) plane.
(III) A silver halide photographic material comprising a support having provided thereon
at least one silver halide emulsion layer containing substantially normal silver halide
grains having a (111) plane and a (100) plane, wherein the (100) plane occupies at
least about 60% of the surface of the grains, the grains being capable of preferentially
forming a latent image on the (100) plane.
[0027] The embodiment (I) according to the present invention will be described in greater
detail below.
[0028] In the present invention, chemical sensitization nuclei, i.e., positions where a
latent image is formed, are formed apart from most of an adsorbed dye under rigid
control. The inventors have found that this can be accomplished by the following two
methods.
(A) A dye which tends to be adsorbed more on a (111) plane than on a (100) plane of
silver halide grains is chosen in accordance with the method hereinafter described,
and silver halide grains are chemically sensitized in the presence of such a dye,
preferably in an amount enough to completely cover the (111) planes. As a result,
a latent image can be formed on planes other than the (111) planes, i.e., planes on
which the dye has not been adsorbed.
(B) A chemical sensitizer (particularly a sulfur sensitizer) which is capable of selectively
chemically sensitizing a (100) plane more than a (111) plane of the silver halide
grains so that a latent image can be formed thereon is chosen in accordance with the
method hereinafter described, and silver halide grains are chemically sensitized with
such a chemical sensitizer. In this case, the addition of the dye which is selectively
adsorbed on the (111) plane as described in the method (A) may be effected either
before or after the chemical sensitization.
[0029] Method (B) requires a chemical sensitizer capable of selectively sensitizing the
(100) plane, while method (A) permits the use of any kind of chemical sensitizers
as described in
Research Disclosure, Nos. 17643 and 13716. It is preferable to use a chemical sensitizer selectively
sensitizing the (100) plane.
[0030] In both methods (A) and (B), as long as the position where a latent image is to be
formed is controlled, a dye which is easily adsorbed on planes other than the (111)
plane or a dye which is evenly adsorbed on all planes may be added, if desired, in
combination with the above-described dye for selective adsorption onto the (111) plane
before or after or during the chemical sensitization.
[0031] In the present invention, a sensitizing dye to be used should be evaluated for its
selective adsorption on a particular plane of silver halide grains, and also the indices
of planes of silver halide grains should be considered. Based on these results and
taking advantage thereof, chemical sensitization nuclei (i.e., positions where a latent
image is to be formed) are formed at a limited position under control to thereby obtain
an excellent light-sensitive silver halide emulsion having been spectrally sensitized.
[0032] In the present invention, chemical sensitization is effected selectively on a (100)
plane while a (111) plane is covered more positively with a sensitizing dye whose
adsorption selectivity has been judged, thus providing a highly refined technique.
[0033] While method (B) requires a compound which chemically sensitizes a (100) plane selectively,
method (A) permits the use of any kind of chemical sensitizers to preferentially form
a latent image at positions other than a (111) plane.
[0034] To accomplish this result, a chemical sensitizer is added after a (111) plane occupying
40% or more of the silver halide grain surface is covered with a sensitizing dye which
is adsorbed selectively on the (111) plane among other planes. Therefore, formation
of effective chemical sensitization nuclei on the (111) plane is inhibited, while
effective chemical sensitization nuclei are formed preferentially on uncovered or
less covered planes other than the (111) plane, for example, a (100) plane. As a result,
a latent image can be formed in a limited position.
[0035] The position where a latent image is to be formed can be limited more strictly by
using the dye in an amount greater than that required for covering the (111) plane
or by using a small amount of a dye which is adsorbed selectively on other planes
in combination.
[0036] Thus, since the position where most of the dye is adsorbed and the position where
a latent image is to be formed can be separated on the surface of silver halide grains,
a large quantity of a dye can be used and a number of common developers having small
solubility can be employed without being accompanied by development delay as encountered
in the case of shallow internal latent image type grains to thereby obtain a high
sensitivity silver halide emulsion.
[0037] In the silver halide emulsion containing substantially normal grains which can be
used in the present invention, at least 40%, preferably at least 60%, more preferably
at least 80% of the grain surface is occupied by a (111) plane, with the surface area
occupied by a (100) plane preferably ranging from about 5 to about 20%.
[0038] In general, the surface of silver halide grains is composed of a (100) plane, a (111)
plane, and a (110) plane and, in most cases, composed of a (100) plane and a (111)
plane. The plane ratio can be obtained by directly observing an electron micrograph
taken of a carbon replica of silver halide grains. For more precise determination,
the method described in
Nippon Kagaku Kaishi, No. 6, 942 (1984) can be adopted, which utilizes the fact that anhydro-3,3′-bis(sulfobutyl)-9-methylthiacarbocyanine
hydroxide pyridinium salt gives a reflective spectrum markedly differing depending
on the plane on which it is adsorbed. That is, the reflective spectra of a thick emulsion
layer containing the above-described dye in varied amounts are obtained and evaluated
using Kubelka-Munk's formula to obtain the ratios of the (100) plane and the (111)
plane.
[0039] The position where a latent image is formed can be discriminated as follows.
[0040] A light-sensitive material composed of a support coated with a silver halide emulsion
is exposed to light at an exposure of from (a) an exposure corresponding to (maximum
density - minimum density) × 1/2 of a characteristic curve of a silver image obtained
when exposed for 1 second and developed with a developer "MAA-1" (produced by Eastman
Kodak Co., Ltd.) at 20°C for 10 minutes to (b) an exposure 1,000 times that exposure.
The exposed material is then developed with an arresting developing solution having
the following formulation at 20°C for 10 minutes. The development time, the pH of
the developing solution, and the amount of a surface active agent used should be varied
depending on the grain size or halogen composition of the silver halide grains so
that fine silver spots indicating development centers may be observed easily.
Arresting Developing Solution Formulation: |
Metol |
0.45 g |
Ascorbic Acid |
3.0 g |
Borax |
5.0 g |
KBr |
1.0 g |
Surface Active Agent (cetyl trimethylammonium chloride) |
0.2 g |
Water to make |
1 liter |
[0041] In cases where development arresting is too strong due to a high iodine content of
the silver halide grains or by the action of a sensitizing dye used, the pH of the
developing solution can be slightly elevated with a sodium hydroxide aqueous solution
or the development time is extended.
[0042] The surface active agent in the arresting developer serves to set the developed silver
which is apt to extend in the form of filaments into masses so as to facilitate judgment
of the position of the developed silver.
[0043] The development is stopped with a 5 wt% aqueous solution of glacial acetic acid and,
without effecting fixation, subjected to enzymatic decomposition using pronase to
recover silver halide grains. Thereafter, a small amount of the material is placed
on a micromesh of an electron microscope. After carbon is vacuum evaporated thereon
to prevent formation of print-out silver, the developed material is fixed with a fixing
solution, and a carbon replica thereof is prepared. The position of remaining developed
silver, i.e., the position where a latent image is formed, is observed under an electron
microscope.
[0044] The phrase "capable of preferentially forming a latent image on the (100) plane"
as used herein means that a major proportion, e.g., 60% or more, preferably 70% or
more, particularly preferably 75% or more, of the fine silver specks formed by the
above-described arrested development is formed on the (100) plane. It is the best
that all of the fine silver specks are formed on the (100) plane. A few fine silver
specks may, however, be formed on the (111) plane in a proportion of less than 40%
and preferably less then 30%.
[0045] The compound capable of chemically sensitizing the (100) plane selectively which
can be used in method (B) can be selected as follows.
[0046] As emulsion comprising tetradecahedral pure silver bromide grains having (111) and
(100) planes in an equal proportion is prepared. The emulsion is chemically sensitized
with a compound under examination to the degree optimum for 1 second exposure and
then subjected to the above-described determination of the latent image position.
An illustrative example for the selection of the chemical sensitizer will be given
in Example 1.
[0047] The compound capable of chemically sensitizing the (100) plane selectively mainly
includes sulfur sensitizers. Such sulfur sensitizers include organic chemical sensitizers,
such as thioureas, rhodanines, oxazolidines, polysulfides and selenoureas. Noble metal
sensitizers, such as gold, platinum, palladium and iridium, can also be used. In addition,
unstable sulfur compounds such as conventional thiosulfates can be used, and particularly
preferably in the presence of the above-described dye which is adsorbed more on the
(111) plane than on the (100) plane.
[0049] The sensitizing dye which is selectively adsorbed onto a (111) plane instead of a
(100) plane of silver halide grains can be determined by the following three methods.
(1) Determination by Absorption Spectrum:
[0050] Octahedral silver bromide grains composed of (111) planes and cubic silver bromide
grains composed of (100) planes are prepared (silver bromide may be replaced by silver
iodobromide or silver chlorobromide). The surface area of each of these grains is
obtained from the respective electron micrograph, and both grains are mixed together
to prepare a silver halide emulsion at such a mixing ratio that the area of the (111)
plane and that of the (100) plane are equal.
[0051] Of methine dyes that are photographically useful and also preferred in the present
invention, those giving different absorption spectra depending on whether they are
adsorbed on a (111) plane or a (100) plane can be evaluated for their selectivity
in adsorption between these two planes from their absorption spectra. That is, the
absorption spectrum of a dye adsorbed on each of the cubic grains and the octahedral
grains is obtained in advance, and the absorption spectrum of the dye when added to
the above-prepared mixed emulsion is then determined, whereby the plane on which the
dye begins to be selectively adsorbed can be judged from the absorption peak wavelength.
[0052] Further, the plane on which the dye begins to be adsorbed can be quantitatively determined
from the resulting spectrum according to the method described in the above-cited
Nippon Kagaku Kaishi, No. 6, 942 (1984).
(2) Determination by Emulsion Separation:
[0053] Octahedral silver bromide grains and cubic silver bromide grains greatly differing
in grain size are mixed so as to have the (111) and (100) planes at an equal area
ratio.
[0054] A dye is added to the resulting mixed emulsion and adsorbed thereon. The emulsion
is then separated into the octahedral grains and the cubic grains, and the amount
of the dye in each separated emulsion is quantitatively determined.
[0055] An example illustrating this method is given in Example 2.
(3) Determination by Photographic Technique:
[0056] Octahedral silver bromide grains and cubic silver bromide grains are mixed so as
to have the (111) planes and (100) planes in equal proportions. The silver bromide
may be replaced by silver iodobromide or silver chlorobromide. The sensitivity of
the octahedral grains should be remarkably lower than that of the cubic grains, so
that only the cubic grains will contribute to the photographic sensitivity of the
mixed emulsion. In more detail, the octahedral grains are doped with rhodium. Even
if a dye is adsorbed on such rhodium-doped octahedral grains to any high degree, spectral
sensitization due to the dye does not occur. It is not until the dye is adsorbed onto
the cubic grains.that spectral sensitivity due to the dye is imparted to the mixed
emulsion.
[0057] As is seen from the foregoing, when a dye which is selectively adsorbed more on a
(111) plane than on a (100) plane is added to the mixed emulsion, since it begins
to be adsorbed first on the octahedral grains, spectral sensitivity cannot be obtained
until the octahedral grains are saturated with the adsorbed dye.
[0058] The cubic grains begin to adsorb the dye to acquire spectral sensitivity after the
saturation of the octahedral grains is reached.
[0059] Then, an emulsion solely composed of cubic grains having the same surface area as
that of the above-prepared mixed emulsion, in which the half of the grains have been
doped with rhodium so as to have an extremely low sensitivity, is prepared, and the
relationship between the amount of a dye added thereto and the spectral sensitivity
obtained is established in advance. A given amount of the added dye being taken as
b, the amount of the dye added to the mixed emulsion which affords the same sensitivity
as that obtained with b is taken as a. When the dye of the amount a is added to the
mixed emulsion, the amount of the dye on the cubic grains and that on the octahedral
grains can be quantitatively obtained as (b/2) and (a - b/2), respectively.
[0060] The inventors have chosen dyes which are adsorbed more easily on a (111) plane than
on a (100) plane in accordance with the above-described three methods of determination.
[0061] Such dyes are preferably chosen from among methine dyes. Specific examples of methine
dyes include cyanine dyes, merocyanine dyes, complex cyanine dyes, complex merocyanine
dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes, and hemioxonol dyes,
with cyanine dyes, merocyanine dyes and complex merocyanine dyes being particularly
useful.
[0062] Any nuclei commonly utilized in cyanine dyes as basic heterocyclic nuclei can be
present in these dyes. Such nuclei include a pyrroline nucleus, an oxazoline nucleus,
a thiazoline nucleus, a pyrrole nucleus, an oxazole nucleus, a thiazole nucleus, a
selenazole nucleus, an imidazole nucleus, a tetrazole nucleus, a pyridine nucleus;
the above-enumerated nuclei to which an alicyclic hydrocarbon ring has been fused;
and the above-enumerated nuclei to which an aromatic hydrocarbon ring has been fused,
e.g., an indolenine nucleus, a benzindolenine nucleus, an indole nucleus, a benzoxazole
nucleus, a naphthoxazole nucleus, a benzothiazole nucleus, a naphthothiazole nucleus,
a benzoselenazole nucleus, a benzimidazole nucleus or a quinoline nucleus. These nuclei
may have a substituent on their ring.
[0063] Merocyanine dyes or complex merocyanine dyes can contain 5- to 6-membered heterocyclic
nuclei having a ketomethylene structure, e.g., a pyrazoline-5-one nucleus, a thiohydantoin
nucleus, a 2-thiooxazolidine-2,4-dione nucleus, a thiazolidine-2,4-dione nucleus,
a rhodanine nucleus or a thiobarbituric acid nucleus.
[0064] The dye to be used in the present invention can be chosen from conventional compounds,
such as those recited in
Research Disclosure, No. 17643, 23, IV (December, 1978) or those described in the publications cited
therein. Typical examples of these methine dyes which can be used preferably are cyanine
dyes, and more particularly thiocyanine dyes, selenacyanine dyes, quinocyanine dyes,
thiaquinocyanine dyes, selenaquinocyanine dyes.
[0065] More preferred cyanine dyes include benzothiacyanines, benzoselenacyanines and benzothiaselenacyanines
each having a halogen substituent (e.g., a chlorine atom) at the 5-position thereof;
thiaquinocyanines or selenaquinocyanines having, on one side thereof, a thiazole or
selenazole ring substituted with a halogen atom at the 5-position thereof; and quinocyanines.
[0066] Particularly preferred among them are those forming J-aggregates on silver halide
grains.
[0067] The amount of these sensitizing dyes is preferably at least an amount enough to saturate
the (111) plane and not more than an amount that saturates all of the (111) and (100)
planes.
[0069] The silver halide which can be used in the present invention may be any of silver
bromide, silver iodobromide, silver iodochlorobromide, silver chlorobromide, silver
iodide, and silver chloride, with silver bromide, silver iodobromide, silver iodochlorobromide,
and silver chlorobromide being particularly preferred. The silver chloride content
is preferably 50 mol% or less.
[0070] Conditions for chemical sensitization according to the present invention are not
particularly limited. The pAg preferably ranges from 6 to 11, more preferably 7 to
10, most preferably 7 to 9.5, and the temperature from 40 to 95°C, more preferably
50 to 85°C.
[0071] The amount of the chemical sensitizers such as a sulfur sensitizer and a gold sensitizer
ranges from 10⁻⁸ to 10⁻³ mol, preferably from 10⁻⁷ to 10⁻⁴ mol, per mol of silver
halide.
[0072] As a gold sensitizer, any known compound, such as a chloroaurate and a potassium
aurothiocyanate, may be employed.
[0073] The individual silver halide grains may be homogeneous throughout the crystal structure
or may have a layered structure composed of an outer shell and a core having different
halogen compositions. Further, the grains may be fused type crystals composed of an
oxide crystal (e.g., PbO) and a silver halide crystal (e.g., silver chloride) or epitaxially
grown crystals, e.g., silver bromide grains on which silver chloride, silver iodobromide
and, silver iodide, is epitaxially grown.
[0074] The silver halide grains in photographic emulsions may have any size distribution
or may be monodisperse. The term "monodispersion" as used herein means a dispersion
system in which 90% of the grains fall within a size range of 60%, preferably 40%,
of the number average particle size. The term "number average particle size" as used
herein means the number average diameter of the projected area of silver halide grains.
[0075] The photographic emulsion of the present invention can be prepared by known techniques
as described, e.g., in P. Glafkides,
Chemie et Physique Photographique (Paul Montel, 1967), G.F. Duffin,
Photographic Emulsion Chemistry (The Focal Press, 1966), and V.L. Zelikman et al.,
Making and Coating Photographic Emulsion (The Focal Press, 1964). In some detail, the emulsion can be prepared by any of an
acid process, a neutral process, an ammonia process, and the like. The reaction between
a soluble silver salt and a soluble halogen salt can be carried out by any of a single
jet method, a double jet method and, a combination thereof,
A reverse mixing method may also be adopted, in which grains are formed in the
presence of excess silver ions. Further, a controlled double jet method, in which
a pAg of a liquid phase where silver halide grains are formed is maintained constant,
may also be used. According to the controlled double jet method, an emulsion of grains
having a regular crystal form and a nearly uniform grain size can be obtained.
[0076] Two or more silver halide emulsions separately prepared may be used as a mixture.
[0077] During the formation of silver halide grains or subsequent physical ripening, a cadmium
salt, a zinc salt, a lead salt, a thallium salt, an iridium salt or a complex salt
thereof, a rhodium salt or a complex salt thereof, an iron salt or a complex salt
thereof may be present in the system. Among them, addition of an iridium salt, a rhodium
salt or an iron salt is preferred. The amount of these compounds may be either small
or large depending on the end use.
[0078] If desired, known silver halide solvents may be used. Examples of the silver halide
solvents include ammonia, potassium thiocyanate, and thioethers or thione compounds
described in US-A-3,271,157 and JP-A-51-12360, JP-A-53-82408, JP-A-53-144319, JP-A-54-100717
and JP-A-54-155828.
[0079] For the purpose of preventing fog during preparation, preservation or photographic
processing of the photographic materials or stabilizing photographic performance properties,
the photographic emulsion can contain various compounds. Such compounds include azoles,
such as benzothiazolium salts, nitroindazoles, triazoles, benzotriazoles, and benzimidazoles
(particularly nitro- or halogen-substituted azoles); heterocyclic mercapto compounds,
e.g., mercaptothiazoles, mercaptobenzothiazoles, mercaptobenzimidazoles, mercaptothiadiazoles,
mercaptotetrazoles (especially 1-phenyl-5-mercaptotetrazole), and mercaptopyrimidines;
the above-enumerated heterocyclic mercapto compounds having a water-soluble group,
e.g., a carboxyl group, a sulfo group; thioketo compounds, e.g., oxazolinethione;
azaindenes, e.g., tetraazaindenes (particularly 4-hydroxy-substituted (1,3,3a,7)tetraazaindenes);
benzenethiosulfonic acid, benzenesulfinic acid; and many other compounds known as
antifoggants or stabilizers. Details are disclosed in E.J. Birr,
Stabilization of Photographic Silver Halide Emulsion (The Focal Press, 1974).
[0080] If desired, sensitizing dyes other than the above-described spectrally sensitizing
dyes in accordance with the present invention may be added to the photographic emulsion
immediately before coating. Such sensitizing dyes include cyanine dyes, merocyanine
dyes, complex cyanine dyes, complex merocyanine dyes, holopolar cyanine dyes, hemicyanine
dyes, styryl dyes, oxonol dyes and hemioxonol dyes. Specific examples of these sensitizing
dyes are described, e.g., in P. Glafkides,
Chimie Photographique, Chapters 35 to 41 (Paul Montel, 2nd Ed., 1957), F.M. Hamer,
The Cyanine and Related Compounds (Interscience), U.S. Patents 2,503,776, 3,459,553 and 3,177,210, and
Research Disclosure, Vol. 176, 17643, 23-IV (December, 1978).
[0081] The hydrophilic colloidal layers of the photographic material produced according
to the present invention may contain various water-soluble dyes as filter dyes or
for prevention of irradiation or for other purposes. Such water-soluble dyes include
oxonol dyes, hemioxonol dyes, styryl dyes, merocyanine dyes, cyanine dyes and azo
dyes, with oxonol dyes, hemioxonol dyes and merocyanine dyes being particularly useful.
[0082] The photographic emulsion layers or other hydrophilic colloidal layers can further
contain organic. or inorganic hardening agents. Examples of the hardening agents include
chromates (e.g., chromium alum, chromium acetate), aldehydes (e.g., formaldehyde,
glyoxal, glutaraldehyde), N-methylol compounds (e.g., dimethylolurea, methyloldimethylhydantoin),
dioxane derivatives (e.g., 2,3-dihydroxydioxane), active vinyl compounds (e.g., 1,3,5-triacryloylhexahydro-s-triazine,
1,3-vinylsulfonyl-2-propanol), active halogen compounds (e.g., 2,4-dichloro-6-hydroxy-s-triazine),
mucohalogenic acids (e.g., mucochloric acid, mucophenoxychloric acid), either individually
or in combination thereof.
[0083] The photographic emulsion layers or other hydrophilic colloidal layers of the photographic
materials may furthermore contain various surface active agents as coating aids or
antistatic agents or for improvement of lubrication, improvement of emulsifying dispersibility,
prevention of adhesion, improvement of photographic characteristics (e.g., acceleration
of development, increase of contrast, and increase of sensitivity).
[0084] Examples of the surface active agent to be added include nonionic surface active
agents, such as saponin (steroid type), alkylene oxide derivatives (e.g., polyethylene
glycol, polyethylene glycol/polypropylene glycol condensation products, polyethylene
glycol alkyl ethers or alkylaryl ethers, polyethylene glycol esters, polyethylene
glycol sorbitan esters, polyalkylene glycol alkylamines or amides, silicon-polyethylene
oxide adducts), glycidol derivatives (e.g., alkenylsuccinic polyglycerides, alkylphenyl
polyglycerides), fatty acid esters of polyhydric alcohols, and alkyl esters of sugars;
anionic surface active agents containing an acid group (e.g., carboxyl, sulfo, phospho,
sulfate and phosphate groups), such as alkylcarboxylates, alkyl sulfonates, alkylbenzenesulfonates,
alkylnaphthalenesulfonates, alkylsulfates, alkyl phosphates, N-acyl-N-alkyltaurines,
sulfosuccinates, sulfoalkylpolyoxyethylene alkylphenyl ethers, polyoxyethylene alkyl
phosphates; amphoteric surface active agents, such as amino acids, aminoalkylsulfonic
acids, aminoalkyl sulfates or phosphates, alkylbetaines, amine oxides; and cationic
surface active agents, such as alkylamine salts, aliphatic or aromatic quaternary
ammonium salts, heterocyclic quaternary ammonium salts, e.g., pyridinium, imidazolium,
and aliphatic or heterocyclic phosphonium or sulfonium salts.
[0085] For the purpose of increasing sensitivity or contrast or accelerating development,
the photographic emulsion layers may contain, for example, polyalkylene oxides or
derivatives thereof (e.g., ethers, esters and amides), thioether compounds, thiomorpholines,
quaternary ammonium salt compounds, urethane derivatives, urea derivatives, imidazole
derivatives and 3-pyrazolidones.
[0086] The photographic layers in the present invention can contain color image-forming
couplers, i.e., compounds capable of developing a color upon oxidative coupling with
an aromatic primary amine developing agent, such as phenylenediamine derivatives,
aminophenol derivatives, and so on. For example, magenta-forming couplers include
5-pyrazolone couplers, pyrazolobenzimidazole couplers, cyanoacetylcoumarone couplers,
and open chain acylacetonitrile couplers. Yellow-forming couplers include acylacetamide
couplers (e.g., benzoylacetanilides and pivaloylacetanilides). Cyan-forming couplers
include naphthol couplers and phenol couplers. Couplers that are nondiffusible due
to a hydrophobic group called a ballast group are preferred. The couplers may be either
2-equivalent or 4-equivalent to a silver ion. In addition to the color-forming couplers,
the photographic materials may further contain colored couplers having a color correction
effect, couplers capable of releasing a development inhibitor on development ("DIR
couplers"), or colorless DIR coupling compounds which produce a colorless coupling
reaction product and release a development inhibitor.
[0087] The photographic material can contain known color fog inhibitors, e.g., hydroquinone
derivatives, aminophenol derivatives, gallic acid derivatives and ascorbic acid derivatives.
[0088] The hydrophilic colloidal layers of the photographic material can contain an ultraviolet
absorbent, such as benzotriazole compounds substituted with an aryl group (e.g., those
described in US-A-3,533,794), 4-thiazolidone compounds (e.g., those described in US-A-3,314,794
and 3,352,681), benzophenone compounds (e.g., those described in JP-A-46-2784), cinnamic
esters (e.g., those described in US-A-3,705,805 and 3,707,375), butadiene compounds
(e.g., those described in US-A-4,045,229), and benzoxidol compounds (e.g., those described
in US-A-3,700,455). In addition, the compounds described in US-A-3,499,762 and JP-A-54-48535
can also be used. In addition, ultraviolet absorbing couplers (e.g., α-naphthol type
cyan couplers) or ultraviolet absorbing polymers may also be employed. A specific
layer may be mordanted with these ultraviolet absorbents.
[0089] In carrying out the present invention, the following known discoloration inhibitors
may be used in combination. The dye image stabilizers may be used either individually
or in combination of two or more thereof. The known discoloration inhibitors include
hydroquinone derivatives, gallic acid derivatives, p-alkoxyphenols, p-hydroxyphenol
derivatives and bisphenol derivatives.
[0090] In addition to the above-mentioned additives, the photographic materials produced
according to the present invention can contain other various known additives, such
as brightening agents, desensitizers, plasticizers, slip agents, matting agents, oils
and mordants. Specific examples of useful additives are described in
Research Disclosure, No. 17643, 22-31 (December, 1978).
[0091] The present invention is applicable to various color and black-and-white silver halide
photographic materials, including color positive films, color papers, color negative
films, color reversal materials (some containing couplers and some not), light-sensitive
materials for plate-making (e.g., lith films), light-sensitive materials for cathode
ray tube displays, X-ray films (especially for direct or indirect photographing),
light-sensitive materials for a colloid transfer process, a silver salt diffusion
transfer process, a dye transfer process, a silver dye bleach process, a print-out
paper process or a heat development process.
[0092] The light exposure for obtaining a photographic image can be effected in a usual
manner. Any of known light sources including infrared light can be used, for example,
natural light (sunlight), a tungstem lamp, a fluorescent lamp, a mercury lamp, a xenon
arc lamp, a carbon arc lamp, a xenon flash lamp, a cathode ray tube flying spot, a
light-emitting diode, a laser beam (e.g., a gas laser, a YAG laser, a dye laser or
a semiconductor laser). The exposure may also be effected using light emitted from
a fluorescent substance excited by electron beams, X-rays, γ-rays or α-rays. The exposure
time ranges from 1/1,000 to 1 second as is usually employed for photographing with
cameras. A shorter exposure time, e.g., 10⁻⁶ to 10⁻⁴ seconds is also employable with
a xenon flash lamp or a cathode ray tube, or a longer exposure may also be used. If
desired, the spectral composition of light for exposure can be controlled by the use
of a color filter.
[0093] The photographic materials can be subjected to development processing according to
known methods using known processing solutions as described, e.g., in
Research Disclosure, No. 17643, 28-30. Depending on purposes, either of black-and-white photographic
processing for forming a silver image or color photographic processing for forming
a color image can be applied.
[0094] Embodiment (II) according to the present invention will be described in greater detail
below.
[0095] In this embodiment, the selective chemical sensitization of the (100) plane can be
carried out in the same manner as described with respect to embodiment (I).
[0096] Determination of a dye which is selectively adsorbed more onto a (100) plane than
on a (111) plane of silver halide grains and a dye which is selectively adsorbed more
onto a (111) plane than on a (100) plane as used in method (A) can also be carried
out in the same manner as described in embodiment (I).
[0097] The dye to be used here for selective adsorption onto a (100) plane can preferably
be selected from methine dyes including cyanine dyes and merocyanine dyes, more preferably
from cyanine dyes. Particularly preferred are benzoxacyanine, benzimidacyanine, benzoxaimidacyanine,
benzoxathiacyanine, benzimidathiacyanine, benzoxaselenacyanine, benzimidaselenacyanine;
and benzothiacyanine, benzoselenacyanine or benzothiaselenacyanine, each of which
may have a substituent other than halogen atoms at the 5-position of the benzene nucleus.
Particularly preferred of these dyes are those forming J-aggregates on the surface
of silver halide grains.
[0099] These dyes for selective adsorption either onto the (100) plane or onto the (111)
plane are used in an amount of from 1 × 10⁻⁷ to 2 × 10⁻³ mol, preferably from 1 ×
10⁻⁶ to 1 × 10⁻³ mol, per mol of silver. The amount of the former dye is preferably
at least an amount sufficient for saturating the (100) planes and not more than an
amount for saturating all the (100) planes and the (111) planes. The amount of the
latter dye is preferably at least an amount enough to saturate the (111) planes.
[0100] Silver halide to be used in embodiment (II) may be any of silver bromide, silver
iodobromide, silver iodochlorobromide, silver chlorobromide, silver iodide and silver
chloride, with silver bromide, silver iodobromide, silver iodochlorobromide, and silver
chlorobromide being particularly preferred. The bromine content is preferably 50 mol%
or more, more preferably 70 mol% or more. The iodine content is preferably 38 mol%
or less, more preferably 20 mol% or less. The chlorine content is preferably 50 mol%
or less, more preferably 30 mol% or less.
[0101] Other constructional factors, of embodiment (II) are the same as in embodiment (I).
[0102] Embodiment (III) according to the present invention will be described in greater
detail below.
[0103] A silver halide emulsion which can be used in embodiment (III) contains substantially
normal crystal grains, with at least about 60%, preferably at least about 65%, more
preferably at least about 70%, of the surface of the substantially normal crystal
grains being composed of a (100) plane. The area occupied by a (111) plane is preferably
not more than about 40%, more preferably not more than about 35%.
[0104] The silver halide to be used here may be any of silver bromide, silver iodobromide,
silver iodochlorobromide, silver chlorobromide, silver iodide and silver chloride,
with silver bromide, silver iodobromide, silver iodochlorobromide and silver chlorobromide
being particularly preferred. The bromine content is preferably 50 mol% or more, more
preferably 70 mol% or more. The iodine content is preferably 38 mol% or less, more
preferably 20 mol% or less. The chlorine content is preferably 50 mol% or less, more
preferably 30 mol% or less.
[0105] Other constructional factors of embodiment (III) are the same as in embodiment (I).
[0106] The present invention is now illustrated in greater detail with reference to the
following examples, but the present invention is not to be construed as being limited
thereto. Unless otherwise indicated, all parts, percents and ratios are by weight.
EXAMPLE 1
[0107] To a gelatin aqueous solution kept at 60°C under vigorous stirring was added ammonia
(25 wt%, 6 cm³), and a silver nitrate aqueous solution (0.88 mol) and a potassium
bromide aqueous solution (0.90 mol) were then added thereto simultaneously. During
the addition, the pAg value of the system was maintained at 7.9. The resulting emulsion
was washed with water and desalted according to a known flocculation method and then
adjusted to a pH of 6.3 and a pAg of 8.5 to obtain a monodisperse tetradecahedral
silver bromide emulsion having a grain size of about 0.8 µm.
[0108] The area proportions of (100) planes and (111) planes of the resulting emulsion were
found to be 52% and 48%, respectively, as determined in accordance with the method
described in
Nippon Kagaku Kaishi, No. 6, 942 (1984).
[0109] Each of the chemical sensitizers shown in Table 1 below was added to the emulsion
in an amount indicated, and the emulsion was subjected to chemical ripening at 60°C
for 60 minutes.
[0110] Thereafter, sodium dodecylbenzenesulfonate as a coating aid, potassium poly(4-sulfostyrene)
as a thickener, and sodium 2,4-dichloro-6-hydroxy-s-triazine as a hardening agent
were added to the emulsion. The resulting coating composition was coated on a cellulose
acetate film support together with a gelatin protective layer by a simultaneous extrusion
method, followed by drying. The resulting samples were designated as Samples 1 to
8.
[0111] Each of Samples 1 to 8 was exposed to light for 1 second through an optical wedge
and developed with a developer "MAA-1" produced by Eastman Kodak Co., Ltd. at 20°C
for 10 minutes.
[0112] Then, each of the samples was uniformly exposed to light at an exposure 100 times
as exposure which provided a midpoint density of the characteristic curve obtained
by the above-described development with "MAA-1", i.e.,
, and then was developed with an arresting developer having the same formulation
as described above at 20°C for 10 minutes. After the development was stopped with
a 5 wt% aqueous solution of acetic acid, the emulsion layer was removed from the coating
by decomposing with pronase, and undeveloped silver halide grains were removed therefrom
to prepare a carbon replica.
[0113] Electron micrographs taken of Samples 1 and 2 are shown in Figures 1 and 2, respectively.
[0114] The plane or site on which the developed silver specks were observed under an electron
microscope for each of Samples 1 to 8 is shown in Table 1.
TABLE 1
Sample No. |
Chemical Sensitizer |
Amount of Chemical Sensitizer (mol/mol of AgX) |
Site of Developed Silver Formation |
1 |
Sodium Thiosulfate |
1.6 × 10⁻⁵ |
(111) plane |
2 |
S-2 |
8 × 10⁻⁶ |
(100) plane |
3 |
" |
1.6 × 10⁻⁵ |
(100) plane |
4 |
S-3 |
8 × 10⁻⁶ |
(100) plane |
5 |
S-4 |
2.0 × 10⁻⁵ |
(100) plane |
6 |
S-5 |
8 × 10⁻⁶ |
(100) plane to the corner edges |
7 |
S-10 |
1.6 × 10⁻⁵ |
(100) plane to the edges, little on (111) plane |
8 |
S-12 |
2.0 × 10⁻⁵ |
(100) plane to the corner edges |
[0115] As is apparent from Table 1, the chemical sensitizers in the present invention, S-2,
S-3, S-4, S-5, S-10 and S-12, formed developed silver specks on the (100) plane to
the corner edges, while sodium thiosulfate formed developed silver specks on the (111)
plane.
[0116] Thus, the site where the chemical sensitizer selectively forms chemical sensitization
nuclei where a latent image is to be formed can be judged.
EXAMPLE 2
[0117] A monodisperse emulsion of octahedral silver iodobromide grains (iodine content:
1 mol%) having a grain size of 2 µm and a monodisperse emulsion of cubic silver iodobromide
grains (iodine content: 1 mol%) having a grain size of 0.5 µm were prepared. The two
emulsions were mixed to prepare a mixed emulsion having (111) planes and (100) planes
in equal proportions.
[0118] The mixed emulsion was spectrally sensitized with each of the sensitizing dyes shown
in Table 2 at a pH of 6.5, a pAg of 8 and a temperature of 60°C for 30 minutes, the
dye being added in an amount of 10 × 10⁻⁵ mol per mol of silver iodobromide which
corresponded to an amount covering about 20% of the total surface area of silver iodobromide
grains, taking the surface area of the grains being 0,7 nm² (70 Ų) per molecule.
The thus-sensitized emulsion was filtered through a filter having a pore size of 0.8
µm, and the amount of the adsorbed dye in the filtrate (emulsion of cubic grains)
was determined. The ratio of the amount of the dye adsorbed to the cubic grains or
the octahedral grains to the amount of the dye added is shown in Table 2.
[0119] The results of Table 2 reveal that almost the whole amount of Comparative Dye (A)
was adsorbed on the surface of the cubic grains, while the dyes in the present invention,
D-2, D-6, D-8, D-10, D-13, D-17, D-20, D-22 and D-23, were not substantially adsorbed
or, if any, a little adsorbed on the cubic grains. From these results, these sensitizing
dyes of the present invention prove to be selectively adsorbed on the (111) plane.
EXAMPLE 3
[0120] The same tetradecahedral silver bromide emulsion as used in Example 1 was chemically
sensitized with a sulfur sensitizer as shown in Table 3 at 60°C for 60 minutes. To
the chemically sensitized emulsion was added a sensitizing dye, D-8 used in the invention,
in an amount of 3 × 10⁻⁴ mol per mol of silver bromide. Thereafter, (4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene)
was added thereto as a stabilizer in an amount of 3 × 10⁻³ mol per mol of silver bromide,
and the same coating aid, thickener and hardening agent as used in Example 1 were
further added. The resulting coating composition was coated on a cellulose acetate
film support simultaneously with a gelatin protective layer. The resulting samples
were designated as Samples 10 to 14.
[0121] Each of Samples 10 to 14 was exposed to light through an optical wedge and a yellow
filter and developed with a developer "Hilendol" (produced by Fuji Photo Film Co.,
Ltd.) at 20°C for 4 minutes. The sensitivity of the sample was obtained as the reciprocal
of an exposure necessary for obtaining a density of fog + 0.2 and relatively expressed
taking the sensitivity of Sample 10 (comparative sample) as a standard (100). The
results obtained are shown in Table 3.
[0122] Separately, the samples were subjected to arrested development in the same manner
as in Example 1 to judge the site where fine silver specks were formed, and the results
obtained are also shown in Table 3.
TABLE 3
Sample No. |
Chemical Sensitizer |
Amount of Chemical Sensitizer (mol/mol-Ag) |
Relative Sensitivity |
Site of Latent Image Formation |
10 |
Sodium Thiosulfate (comparison) |
1.6 × 10⁻⁵ |
100 |
(111) plane |
11 |
S-2 |
8 × 10⁻⁶ |
795 |
(100) plane |
12 |
S-3 |
8 × 10⁻⁶ |
890 |
(100) plane |
13 |
S-5 |
8 × 10⁻⁶ |
630 |
(100) plane to the corner edges |
14 |
S-10 |
1.6 × 10⁻⁵ |
570 |
(100) plane to the corner edges |
[0123] As is apparent from Table 3, the photographic sensitivity was markedly increased
when a latent image was formed on the plane other than the (111) plane, i.e., the
(100) plane.
EXAMPLE 4
[0124] A monodisperse tetradecahedral silver iodobromide emulsion (iodine content: 2 mol%,
grain size: about 0.6 µm) composed of 38% of a (100) plane and 62% of a (111) plane
was prepared in the same manner as described in Example 1, except for maintaining
the grain formation system at a pAg of 8.1. After water washing and desalting, the
emulsion was adjusted to a pH of 6.5 and a pAg of 8.5.
[0125] The resulting emulsion was divided into four portions, designated as Emulsions A,
B, C and D.
[0126] Emulsion A was chemically sensitized with sodium thiosulfate, chloroauric acid and
potassium thiocyanate at 60°C for 60 minutes, and then a sensitizing dye used in the
invention (D-8) and two kinds of sensitizing dyes having the formulae shown below
were added thereto in amounts of 3.5 × 10⁻⁴ mol, 1 × 10⁻⁵ mol, and 1 × 10⁻⁴ mol, each
per mol of silver.
[0127] On examination of the above-described two dyes in accordance with the method described
above they were found to be selectively adsorbed on the (100) plane.
[0128] Emulsion B was chemically sensitized with a sulfur sensitizer, S-2, chloroauric acid
and potassium thiocyanate, and the same three dyes as used for Emulsion A were then
added thereto.
[0129] To Emulsion C was added D-8, and the emulsion was chemically sensitized with sodium
thiosulfate, chloroauric acid, and potassium thiocyanate at 60°C for 60 minutes. Then,
the two other dyes were added thereto.
[0130] To Emulsion D was added D-8, and the emulsion was chemically sensitized with S-2,
chloroauric acid, and potassium thiocyanate at 60°C for 60 minutes. Then, the two
other dyes were added thereto.
[0131] To each of the emulsions were added couplers (C-6 and C-7), dispersing oils (Oil-1
and Oil-2), an antifoggant (1-(m-sulfophenyl)-5-mercaptotetrazole monosodium salt),
and a stabilizer (4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene). The same coating aid,
thickener and hardening agent as used in Example 1 were further added thereto. The
resulting coating composition was coated on a cellulose acetate film support together
with a gelatin protective layer.
[0132] The resulting sample was exposed to light through an optical wedge and a yellow filter
and subjected to color development processing according to the procedure shown below
at 38°C.
[0133] The compounds used in the sample preparation were as follows.
Processing Procedure: |
Color Development |
2 min 45 sec |
Bleach |
6 min 30 sec |
Washing |
2 min 10 sec |
Fixation |
4 min 20 sec |
Washing |
3 min 15 sec |
Stabilization |
1 min 05 sec |
Color Developer Formulation: |
Diethylenetriaminepentaacetic Acid |
1.0 g |
1-Hydroxyethylidene-1,1-diphosphonic Acid |
2.0 g |
Sodium Sulfate |
4.0 g |
Potassium Carbonate |
30.0 g |
Potassium Bromide |
1.4 g |
Potassium Iodide |
1.3 mg |
Hydroxylamine Sulfate |
2.4 g |
4-(N-Ethyl-N-β-hydroxyethylamino)-2-methylaniline Sulfate |
4.5 g |
Water to make |
1.0 liter |
|
pH = 10.0 |
Bleaching Solution Formulation: |
Ammonium (Ethylenediaminetetraacetato)Ferrite |
100.0 g |
Disodium Ethylenediaminetetraacetate |
10.0 g |
Ammonium Bromide |
150.0 g |
Ammonium Nitrate |
10.0 g |
Water to make |
1.0 liter |
|
pH = 6.0 |
Fixing Solution Formulation: |
Disodium Ethylenediaminetetraacetate |
1.0 g |
Sodium Sulfite |
4.0 g |
Ammonium Thiosulfate (70 wt% aq. soln.) |
175.0 mℓ |
Sodium Bisulfite |
4.6 g |
Water to make |
1.0 liter |
|
pH = 6.6 |
Stabilizer Formulation: |
Formalin (40 wt%) |
2.0 mℓ |
Polyoxyethylene-p-monononylphenyl Ether (average degree of polymerization: 10) |
0.3 g |
Water to make |
1.0 liter |
[0134] The relative sensitivity of each sample is shown in Table 4 below, taking the sensitivity
of Emulsion A as a standard (100). The site for latent image formation was determined
in the same manner as in Example 2 and is also shown in Table 4.
TABLE 4
Emulsion |
Relative Sensitivity |
Site of Latent Image Formation |
Remarks |
A |
100 |
Predominantly on (111) plane, a few on (100) plane |
Comparison |
B |
131 |
Predominantly on (100) plane, a few on (111) plane |
Invention |
C |
148 |
Predominantly on (100) plane |
Invention |
D |
153 |
Predominantly on (100) plane |
Invention |
[0135] As is apparent from the Table, when the emulsion contained a large amount of D-8
which is selectively adsorbed on (111) plane, the site for latent image formation
was predominantly formed on the plane other than the (111) plane, i.e., the (100)
plane, and the emulsion had high sensitivity.
EXAMPLE 5
[0136] Emulsions A and D as prepared in Example 4 were treated in the same manner as in
Example 4, except for replacing D-8 with D-17, D-18 or D-20, and tested in the same
manner as in Example 4. As a result, Emulsion D proved more highly sensitive than
Emulsion A in each case.
EXAMPLE 6
[0137] Silver bromide was grown as an outer shell on seed crystals of silver iodobromide
having an iodine content of 30 mol% to prepare Emulsion E and Emulsion F comprising
core/shell grains both having a silver iodide content of 10 mol% and each having a
grain size of 0.7 µm and 1.5 µm, respectively.
[0138] Emulsion E grains were composed of 20% of a (100) plane and 80% of a (111) plane,
while Emulsion F grains were composed of 15% of a (100) plane and 85% of a (111) plane,
both being monodisperse tetradecahedra close to octahedra.
[0139] After adjustment to a pH of 6.3 and a pAg of 8.9, each of Emulsions E and F was divided
into two portions, designated as Emulsions E-1 and E-2 and Emulsions F-1 and F-2,
respectively.
[0140] Emulsion E-1 was chemically sensitized with sodium thiosulfate and chloroauric acid,
and Dyes I, II and III were added thereto. To Emulsion E-2 was first added Dye II
(corresponding to D-8), the emulsion was sensitized with sodium thiosulfate and chloroauric
acid, and Dyes I and III were then added thereto.
[0141] Emulsion F-1 was chemically sensitized with sodium thiosulfate and chloroauric acid,
and Dye IX was then added thereto. To Emulsion F-2 was added Dye IX (corresponding
to D-2) and the emulsion was then chemically sensitized with a sulfur sensitizer,
S-3, and chloroauric acid.
[0142] Each of these sensitized emulsions was coated on a support in a single layer. On
examination by the arrested development process in the same manner as in Example 2,
it was proved that Emulsions E-2 and F-2 both formed fine developed silver specks
in the neighborhood of the corners of individual grains, i.e., on the (100) plane,
while Emulsions E-1 and F-1 both formed developed silver specks over the entire surface
of the grains.
[0143] A multilayer color light-sensitive material having a layer structure described below
was prepared using Emulsion E-1 in the fifth layer and Emulsion F-1 in the twelfth
layer or using Emulsion E-2 in the fifth layer and Emulsion F-2 in the twelfth layer.
The resulting samples were designated as Sample 20 and Sample 21, respectively.
[0144] Each of Samples 20 and 21 was exposed to light at 25 CMS using a tungsten lamp (color
temperature adjusted to 4,800 K through a filter) and subjected to development processing
at 38°C according to the following procedure.
Processing Procedure: |
Color Development |
3 min 15 sec |
Bleach |
6 min 30 sec |
Washing |
2 min 10 sec |
Fixation |
4 min 20 sec |
Washing |
3 min 15 sec |
Stabilization |
1 min 05 sec |
[0145] The processing solutions used in the development processing had the same formulations
as used in Example 4.
Layer Structure:
[0146]
First Layer: Antihalation Layer |
Black colloidal silver |
0.2 g-Ag/m² |
Gelatin |
1.3 g/m² |
Colored coupler, C-1 |
0.06 g/m² |
Ultraviolet absorbent, UV-1 |
0.1 g/m² |
Ultraviolet absorbent, UV-2 |
0.2 g/m² |
Dispersing oil, Oil-1 |
0.01 g/m² |
Dispersing oil, Oil-2 |
0.01 g/m² |
Second Layer: Intermediate Layer |
Silver bromide fine grains (mean grain size: 0.07 µm) |
0.15 g-Ag/m² |
Gelatin |
1.0 g/m² |
Colored coupler, C-2 |
0.02 g/m² |
Dispersing oil, Oil-1 |
0.1 g/m² |
Third Layer: First Red-Sensitive Emulsion Layer |
Silver iodobromide emulsion (silver iodide: 2 mol%, mean grain size: 0.3 µm) |
0.4 g-Ag/m² |
Gelatin |
0.6 g/m² |
Sensitizing Dye I |
1.0×10⁻⁴ mol/mol-AgX |
Sensitizing Dye II |
3.0×10⁻⁴ mol/mol-AgX |
Sensitizing Dye III |
1×10⁻⁵ mol/mol-AgX |
Coupler, C-3 |
0.06 g/m² |
Coupler, C-4 |
0.06 g/m² |
Coupler, C-8 |
0.04 g/m² |
Coupler, C-2 |
0.03 g/m² |
Dispersing oil, Oil-1 |
0.03 g/m² |
Dispersing oil, Oil-3 |
0.012 g/m² |
Fourth Layer: Second Red-Sensitive Emulsion Layer |
Silver iodobromide emulsion (silver iodide: 5 mol%, mean grain size: 0.5 µm) |
0.7 g-Ag/m² |
Gelatin |
0.6 g/m² |
Sensitizing Dye I |
1×10⁻⁴ mol/mol-AgX |
Sensitizing Dye II |
3×10⁻⁴ mol/mol-AgX |
Sensitizing Dye III |
1×10⁻⁵ mol/mol-AgX |
Coupler, C-3 |
0.24 g/m² |
Coupler, C-4 |
0.24 g/m² |
Coupler, C-8 |
0.04 g/m² |
Coupler, C-2 |
0.04 g/m² |
Dispersing oil, Oil-1 |
0.15 g/m² |
Dispersing oil, Oil-3 |
0.02 g/m² |
Fifth Layer: Third Red-Sensitive Emulsion Layer |
Emulsion E (silver iodide: 10 mol%, mean grain size: 0.7 µm) |
1.0 g-Ag/m² |
Gelatin |
1.0 g/m² |
Sensitizing Dye I |
1×10⁻⁴ mol/mol-AgX |
Sensitizing Dye II (corresponding to D-8) |
3×10⁻⁴ mol/mol-AgX |
Sensitizing Dye III |
1×10⁻⁵ mol/mol-AgX |
Coupler, C-5 |
0.05 g/m² |
Coupler, C-7 |
0.1 g/m² |
Dispersing oil, Oil-1 |
0.01 g/m² |
Dispersing oil, Oil-2 |
0.05 g/m² |
Sixth Layer: Intermediate Layer |
Gelatin |
1.0 g/m² |
Compound, Cpd-A |
0.03 g/m² |
Dispersing oil, Oil-1 |
0.05 g/m² |
Seventh Layer: First Green-Sensitive Emulsion Layer |
Silver iodobromide emulsion (silver iodide: 4 mol%, mean grain size: 0.3 µm) |
0.30 g-Ag/m² |
Sensitizing Dye IV |
5×10⁻⁴ mol/mol-AgX |
Sensitizing Dye VI |
0.3×10⁻⁴ mol/mol-AgX |
Sensitizing Dye V |
2×10⁻⁴ mol/mol-AgX |
Gelatin |
1.0 g/m² |
Coupler, C-9 |
0.2 g/m² |
Coupler, C-5 |
0.03 g/m² |
Coupler, C-1 |
0.03 g/m² |
Dispersing oil, Oil-1 |
0.5 g/m² |
Eighth Layer: Second Green-Sensitive Emulsion Layer |
Silver iodobromide emulsion (silver iodide: 5 mol%, mean grain size: 0.5 µm) |
0.4 g-Ag/m² |
Sensitizing Dye IV |
5×10⁻⁴ mol/mol-AgX |
Sensitizing Dye V |
2×10⁻⁴ mol/mol-AgX |
Sensitizing Dye VI |
0.3×10⁻⁴ mol/mol-AgX |
Coupler, C-9 |
0.25 g/m² |
Coupler, C-1 |
0.03 g/m² |
Coupler, C-10 |
0.015 g/m² |
Coupler, C-5 |
0.01 g/m² |
Dispersing oil, Oil-1 |
0.2 g/m² |
Ninth Layer: Third Green-Sensitive Emulsion Layer |
Silver iodobromide emulsion (silver iodide: 6 mol%, mean grain size: 0.7 µm) |
0.85 g-Ag/m² |
Gelatin |
1.0 g/m² |
Sensitizing dye VII |
3.5×10⁻⁴ mol/mol-AgX |
Sensitizing Dye VIII |
1.4×10⁻⁴ mol/mol-AgX |
Coupler, C-11 |
0.01 g/m² |
Coupler, C-12 |
0.03 g/m² |
Coupler, C-13 |
0.20 g/m² |
Coupler, C-1 |
0.02 g/m² |
Coupler, C-15 |
0.02 g/m² |
Dispersing oil, Oil-1 |
0.20 g/m² |
Dispersing oil, Oil-2 |
0.05 g/m² |
Tenth Layer: Yellow Filter Layer |
Gelatin |
1.2 g/m² |
Yellow colloidal silver |
0.08 g-Ag/m² |
Compound, Cpd-B |
0.1 g/m² |
Dispersing oil, Oil-1 |
0.3 g/m² |
Eleventh Layer: First Blue-Sensitive Emulsion Layer |
Monodisperse silver iodobromide emulsion (silver iodide: 4 mol%, mean grain size:
0.3 µm) |
0.4 g-Ag/m² |
Gelatin |
1.0 g/m² |
Sensitizing Dye IX |
2×10⁻⁴ mol/mol-AgX |
Coupler, C-14 |
0.9 g/m² |
Coupler, C-5 |
0.07 g/m² |
Dispersing oil, Oil-1 |
0.2 g/m² |
Twelfth Layer: Second Blue-Sensitive Emulsion Layer |
Emulsion F (silver iodide: 10 mol%, mean grain size: 1.5 µm) |
0.5 g-Ag/m² |
Gelatin |
0.6 g/m² |
Sensitizing Dye IX (corresponding to D-2) |
1×10⁻⁴ mol/mol-AgX |
Coupler, C-14 |
0.25 g/m² |
Dispersing oil, Oil-1 |
0.07 g/m² |
Thirteenth Layer: First Protective layer |
Gelatin |
0.8 g/m² |
Ultraviolet absorbent, UV-1 |
0.1 g/m² |
Ultraviolet absorbent, UV-2 |
0.2 g/m² |
Dispersing oil, Oil-1 |
0.01 g/m² |
Dispersing oil, Oil-2 |
0.01 g/m² |
Fourteenth Layer: Second Protective Layer |
Fine silver bromide grains (mean grain size: 0.07 µm) |
0.5 g/m² |
Gelatin |
0.45 g/m² |
Polymethyl methacrylate particles (diameter: 1.5 µm) |
0.2 g/m² |
Hardening agent, H-1 |
0.4 g/m² |
Formaldehyde scavenger, S′-1 |
0.5 g/m² |
Formaldehyde scavenger, S′-2 |
0.5 g/m² |
[0147] Each of the layers additionally contained a surface active agent as a coating aid.
[0149] The results obtained are shown in Table 5 below. In the Table, "relative sensitivity"
is the reciprocal of an exposure providing a color density of fog + 0.1, taking the
sensitivity of Sample 20 as a standard (100).
TABLE 5
Sample No. |
Emulsion |
Relative Sensitivity |
|
5th Layer |
12th Layer |
Cyan-Forming Layer |
Yellow-Forming Layer |
20 |
E-1 |
F-1 |
100 |
100 |
21 (Invention) |
E-2 |
F-2 |
126 |
132 |
[0150] As is apparent from Table 5, when a dye capable of being selectively adsorbed on
a (111) plane was used, the emulsion produced in the process of the present invention
which selectively forms a latent image on a (100) plane exhibited higher sensitivity
than the other emulsion.
EXAMPLE 7
[0151] A monodisperse emulsion of octahedral silver iodobromide grains (iodine content:
1 mol%) having a grain size of 2 µm and a monodisperse emulsion of cubic silver iodobromide
grains (iodine content: 1 mol%) having a grain size of 0.5 µm were prepared. The two
emulsions were mixed to prepare a mixed emulsion having (111) planes and (100) planes
in equal proportions.
[0152] The mixed emulsion was spectrally sensitized with each of the sensitizing dyes shown
in Table 6 at a pH of 6.5, a pAg of 8.4 and a temperature of 60°C for 30 minutes,
the dye being added in an amount of 10 × 10⁻⁵ mol per mol of silver iodobromide which
corresponded to an amount covering about 20% of the total surface area of silver iodobromide
grains, taking the surface area of the grains as 0,7 nm² (70 Ų) per molecule.
[0153] The thus-sensitized emulsion was filtered through a filter having a pore size of
0.8 µm, and the amount of the adsorbed dye in the filtrate (emulsion of cubic grains)
was determined. The ratio of (a) the amount of the dye adsorbed to the cubic grains
or the octahedral grains to (b) the amount of the dye added is shown in Table 6.
TABLE 6
Dye |
Ratio of Dye Adsorbed Based on Added Dye |
|
On Cubic Grains (%) |
On Octahedral Grains (%) |
E-14 |
ca. 100 |
ca. 0 |
E-1 |
98 |
2 |
E-2 |
ca. 100 |
ca. 0 |
E-3* |
75 |
25 |
E-7 |
ca. 100 |
ca. 0 |
E-11 |
ca. 100 |
ca. 0 |
E-13 |
96 |
4 |
E-16 |
ca. 100 |
ca. 0 |
E-20 |
62 |
38 |
E-21 |
ca. 100 |
ca. 0 |
E-22 |
ca. 100 |
ca. 0 |
E-25 |
94 |
6 |
E-27 |
98 |
2 |
D-2 |
5 |
95 |
E-5 |
2 |
98 |
D-6 |
ca. 0 |
ca. 100 |
D-8 |
ca. 0 |
ca. 100 |
D-10 |
5 |
95 |
D-20 |
ca. 0 |
ca. 100 |
D-23 |
5 |
95 |
Note: * 5 Minutes before the addition of E-3, 216 mg/mol-Ag of potassium iodide was
added to the emulsion. |
[0154] From the results of Table 6, it can be seen that the dyes designated "E" were not
substantially or, if any, slightly adsorbed onto the octahedral grains, i.e., they
preferentially were adsorbed onto (100) planes, while the dyes designated "D" started
to be adsorbed onto (111) planes, just the opposite to the "E" dyes.
[0155] Thus, whether a dye is selectively adsorbed on a (100) plane or a (111) plane of
silver halide grains can be quantitatively judged.
EXAMPLE 8
[0156] The tetradecahedral silver bromide emulsion as prepared in Example 1 was chemically
sensitized with a sulfur sensitizer as shown in Table 7 at 60°C for 60 minutes. Then,
E-2 was added thereto in an amount of 3 × 10⁻⁴ mol per mol of silver bromide. A stabilizer
(4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene; 4 × 10⁻³ mol/mol AgBr) and the same coating
aid, thickener and hardening agent as used in Example 1 were further added to the
emulsion. The resulting coating composition was coated on a cellulose acetate film
support together with a gelatin protective layer. The resulting light-sensitive materials
were designated as Samples 22 to 26.
[0157] Each of Samples 22 to 26 was exposed to light through an optical wedge and a yellow
filter and developed with a developer "Hilendol" at 20°C for 4 minutes. The results
obtained are shown in Table 7, in which "relative sensitivity" is the reciprocal of
an exposure providing a density of fog + 0.2, taking the sensitivity of Sample 22
as a standard (100).
[0158] The site of fine developed silver specks, as determined by the arrested development
method described in Example 1, is also shown in Table 7.
TABLE 7
Sample No. |
Chemical Sensitizer |
Amount of Chemical Sensitizer (mol/mol-Ag) |
Relative Sensitivity |
Site of Latent Image Formation |
22 |
Sodium Thiosulfate (comparison) |
1.6 × 10⁻⁵ |
100 |
(111) plane |
23 |
S-2 |
8 × 10⁻⁶ |
250 |
(100) plane |
24 |
S-3 |
8 × 10⁻⁶ |
280 |
(100) plane |
25 |
S-5 |
8 × 10⁻⁶ |
205 |
(100) plane to the corner edges |
26 |
S-10 |
1.6 × 10⁻⁵ |
190 |
(100) plane to the corner edges |
[0159] It can be seen from Table 7 that formation of a latent image on planes other than
(111) planes, i.e., on (100) planes resulted in markedly increased sensitivity.
EXAMPLE 9
[0160] Emulsions A, B, C and D as prepared in Example 4 were used.
[0161] Emulsion A was chemically sensitized with sodium thiosulfate, chloroauric acid, and
potassium thiocyanate at 60°C for 60 minutes, and then E-1 and D-2 were added thereto
in an amount of 2.5 × 10⁻⁴ mol and 2.0 × 10⁻⁴ mol, respectively, each per mol of silver.
[0162] Emulsion B was chemically sensitized with S-2, chloroauric acid, and potassium thiocyanate,
and the same amounts of the same dyes as used above were then added thereto.
[0163] D-2 was first added to Emulsion C, and the emulsion was chemically sensitized with
sodium thiosulfate, chloroauric acid, and potassium thiocyanate at 60°C for 60 minutes.
Then, E-1 was added thereto.
[0164] D-2 was first added to Emulsion D, and the emulsion was chemically sensitized with
S-2, chloroauric acid, and potassium thiocyanate at 60°C for 60 minutes. Then, E-1
was added thereto.
[0165] To each of the emulsions were added couplers (C-1, C-11, C-13 and C-15), dispersing
oils (Oil-1 and Oil-2), an antifoggant (1-(m-sulfophenyl)-5-mercaptotetrazole monosodium
salt), and a stabilizer (4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene). The same coating
aid, thickener and hardening agent as used in Example 1 were further added thereto.
The resulting coating composition was coated on a cellulose acetate film support together
with a gelatin protective layer.
[0166] The resulting sample was exposed to light through an optical wedge and a yellow filter
and subjected to color development processing according to the same procedure as in
Example 4. The results obtained are shown in Table 8, in which the sensitivity is
relatively expressed taking that of Emulsion A as a standard (100). Further, the site
of a latent image formation was examined in the same manner as in Example 7 and the
results are also shown in Table 8.
[0167] The compounds used in the sample preparation are the same as those used in Example
6.
TABLE 8
Emulsion |
Relative Sensitivity |
Site of Latent Image Formation |
A |
100 |
Predominantly on (111) plane, a few on (100) plane |
B |
118 |
Predominantly on (100) plane, a few on (111) plane |
C |
126 |
Predominantly on (100) plane |
D |
132 |
Predominantly on (100) plane |
[0168] As is apparent from Table 8, when E-1 which is selectively adsorbed on (100) planes
was used as a sensitizing dye, emulsions which form sites where a latent image is
formed on planes other than a (111) plane, i.e., (100) planes, exhibited higher sensitivity.
[0169] It is also demonstrated that chemical sensitization could be selectively effected
on (100) planes while (111) planes were covered with D-2 which is selectively adsorbed
on the (111) planes, though making no contribution to spectral sensitivity to light
transmitted by a yellow filter.
EXAMPLE 10
[0170] A tetradecahedral silver bromide emulsion was prepared in the same manner as in Example
1, except for maintaining the pAg of the grain formation system at 7.8. The surface
of the silver bromide grains was found to be composed of 67% of a (100) plane and
33% of a (111) plane.
[0171] After adjustment to a pH of 6.3 and a pAg of 8.5, the emulsion was chemically sensitized
with a sulfur sensitizer as shown in Table 9 at 60°C for 60 minutes. Then, a sensitizing
dye, D-8, was added to the emulsion in an amount of 3 × 10⁻⁴ mol per mol of silver
bromide. A stabilizer (4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene; 4 × 10⁻³ mol/mol
AgBr) and the same coating aid, thickener and hardening agent as used in Example 1
were further added thereto. The resulting coating composition was coated on a cellulose
acetate film support together with a gelatin protective layer. The resulting light-sensitive
materials were designated as Samples 27 to 31.
[0172] Each of Samples 27 to 31 was exposed to light through an optical wedge and a yellow
filter and developed with "Hilendol" at 20°C for 4 minutes. The results obtained are
shown in Table 9, in which "relative sensitivity" is the reciprocal of an exposure
providing a density of fog + 0.2, taking the sensitivity of Sample 27 as a standard
(100). Table 9 also shows the site of fine developed silver specks as determined in
the same manner as in Example 1.
TABLE 9
Sample No. |
Chemical Sensitizer |
Amount of Chemical Sensitizer (mol/mol-Ag) |
Relative Sensitivity |
Site of Latent Image Formation |
27 |
Sodium Thiosulfate (comparison) |
2.4 × 10⁻⁵ |
100 |
(111) plane, a few on (100) plane |
28 |
S-2 |
8 × 10⁻⁶ |
316 |
(100) plane |
29 |
S-3 |
8 × 10⁻⁶ |
352 |
(100) plane |
30 |
S-5 |
1.2 × 10⁻⁵ |
178 |
(100) plane to the edges |
31 |
S-10 |
1.6 × 10⁻⁵ |
162 |
(100) plane to the edges |
EXAMPLE 11
[0173] A monodisperse tetradecahedral silver iodobromide emulsion (iodine content: 2 mol%,
grain size: about 0.6 µm) having 65% of a (100) plane and 35% of a (111) plane was
prepared in the same manner as in Example 10. After washing with water and desalting,
the emulsion was adjusted to a pH of 6.5 and a pAg of 8.5. The emulsion was divided
into four portions, designated as Emulsions G, H, I and J.
[0174] Emulsion G was chemically sensitized with sodium thiosulfate, chloroauric acid, and
potassium thiocyanate at 60°C for 60 minutes, and then D-8, E-13 and E-20 were added
thereto in an amount of 2.5 × 10⁻⁴ mol, 1 × 10⁻⁵ mol, and 1.0 × 10⁻⁴ mol, respectively,
each per mol of silver.
[0175] Emulsion H was chemically sensitized with S-2, chloroauric acid, and potassium thiocyanate,
and then the same amounts of the same dyes as added to Emulsion G were added thereto.
[0176] D-8 was first added to Emulsion I, and the emulsion was sensitized with sodium thiosulfate,
chloroauric acid, and potassium thiocyanate at 60°C for 60 minutes. E-13 and E-20
were then added to the emulsion.
[0177] After D-8 was added to Emulsion J, Emulsion J was chemically sensitized with S-2,
chloroauric acid, and potassium thiocyanate at 60°C for 60 minutes. E-13 and E-20
were then added thereto.
[0178] To each of the emulsions were added couplers (C-6 and C-7), dispersing oils (Oil-1
and Oil-2), an antifoggant (1-(m-sulfophenyl)-5-mercaptotetrazole monosodium salt;
2 × 10⁻⁴ mol/mol silver halide), a stabilizer (4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene;
3 × 10⁻³ mol/mol silver halide), and the same coating aid, thickener and hardening
agent as used in Example 1. The resulting coating composition was coated on a cellulose
acetate film support together with a gelatin protective layer to prepare a light-sensitive
material.
[0179] The couplers and dispersing oils used in this example were the same as used in Example
6.
[0180] Each of the samples was exposed to light through an optical wedge and a yellow filter
and development-processed in the same manner as in Example 4. The results obtained
are shown in Table 10. The site for latent image formation was determined by arrested
development in the same manner as in Example 1, and the results are also shown in
Table 10.
TABLE 10
Emulsion |
Relative Sensitivity of Cyan Dye Image |
Site for Latent Image Formation |
G |
100 |
Predominantly on (111) plane, a few on (100) plane |
H |
115 |
Predominantly on (100) plane, slightly on (111) plane |
I |
120 |
(100) plane |
J |
123 |
(100) plane |
[0181] It can be seen from Table 10 that the emulsions which formed a latent image selectively
on (100) planes exhibited higher sensitivity than those forming a latent image selectively
on (111) planes. In other words, higher spectral sensitivity was obtained by using
a sulfur sensitizer capable of selectively sensitizing a (100) plane than using sodium
thiosulfate which selectively sensitized a (111) plane, or by adding a dye capable
of being selectively adsorbed on a (111) plane and then chemically sensitizing a (100)
plane selectively.
EXAMPLE 12
[0182] Emulsions G and J as prepared in Example 11 were treated in the same manner as in
Example 11, except for replacing D-8 with D-17, D-18 or D-20, and tested in the same
manner as in Example 11.
[0183] As a result, Emulsion J proved more highly sensitive than Emulsion G in any case.
EXAMPLE 13
[0184] Silver bromide was grown as an outer shell on seed crystals of silver iodobromide
having an iodine content of 18 mol% to prepare a monodisperse emulsion containing
tetradecahedral core/shell grains having a silver iodide content of 4.5 mol% and a
mean grain size of 0.8 µm and composed of 72% of a (100) plane and 28% of a (111)
plane. The resulting emulsion was designated as Emulsion K. After adjusting the pH
to 6.3 and the pAg to 8.5, Emulsion K was divided into four portions, designated as
K-1, K-2, K-3 and K-4.
[0185] Emulsion K-1 was chemically sensitized with sodium thiosulfate, chloroauric acid,
and potassium thiocyanate, and then E-1, E-11 and D-2 were added thereto.
[0186] Emulsion K-2 was chemically sensitized with S-3, chloroauric acid, and potassium
thiocyanate, and then E-1, E-11 and D-2 were added thereto.
[0187] D-2 was first added to Emulsion K-3, and the emulsion was chemically sensitized with
sodium thiosulfate, chloroauric acid and potassium thiocyanate. Thereafter, E-1 and
E-11 were added to the emulsion.
[0188] D-2 was first added to Emulsion K-4, and the emulsion was chemically, sensitized
with S-3, chloroauric acid and potassium thiocyanate. Thereafter, E-1 and E-11 were
added thereto.
[0189] Each of the thus-sensitized emulsions was coated on a support in a single layer and
subjected to arrested development. As a result, it was confirmed that Emulsions K-2,
K-3 and K-4, and particularly K-3 and K-4, formed developed silver specks on (100)
planes, while Emulsion K-1 formed developed silver specks on the entire surface of
the grains, and particularly on corners of the grains, i.e., on (111) planes.
[0190] Then, a multilayer color light-sensitive material was prepared having the same layer
structure as described in Example 6, except for replacing the emulsion of the ninth
layer with Emulsion K-1, K-2, K-3 or K-4. The resulting samples were designated as
Samples 32, 33, 34 and 35, respectively.
[0191] Each of Samples 32 to 35 was exposed to light at 25 CMS using a tungsten lamp (color
temperature adjusted to 4,800°K through a filter) and then subjected to the same development
processing at 38°C as described in Example 4. The results obtained are shown in Table
11, in which the relative sensitivity is the reciprocal of an exposure providing a
color density of fog + 0.1, taking the sensitivity of Sample 32 as a standard (100).
TABLE 11
Sample No. |
Relative Sensitivity of Magenta-Forming Layer |
32 |
100 |
33 |
110 |
34 |
115 |
35 |
115 |
[0192] As is apparent from Table 11, emulsions forming a latent image on a (100) plane exhibited
higher sensitivity than other emulsions.