Silver halide reversal photographic light-sensitive material

FIELD OF THE INVENTION
This invention relates to a silver halide reversal photographic light-sensitive material and, more particularly, to a color reversal light-sensitive material improved on color reproduction and gradation.
BACKGROUND OF THE INVENTION
A silver halide reversal photographic light-sensitive material has been required so far to have a variety of characteristics. It has therefore been essential that a silver halide reversal photograph is to be provided with improved color reproduction and more desirable gradation so as to meet the demands for making an image quality higher.
In the case of silver halide reversal photographic light-sensitive materials, it has practically been impossible to apply a technique of compensating the side-absorption of a coloring matter by making use of such a colored coupler as those having been applied to a color negative light-sensitive material but a development effect has mainly been utilized instead. Namely, there has utilized such an effect that the development of the silver halide in one emulsion layer inhibits those in the other layers, that is so-called an interimage effect (hereinafter abbreviated to an IIE). Because one of the most popular development-inhibiting substances is iodine ion, there have been well-known techniques for increasing IIE, in which, for example, the iodide contents of silver halide emulsions are controlled separately by each layer, or the silver iodide contents of both of the surfaces and insides of silver halide grains are adjusted. Also, Japanese Patent Examined Publication No. 35011-1984 and Japanese Patent Publication Open to Public Inspection (hereinafter referred to as Japanese Patent O.P.I. Publication) No. 91946-1987 disclose the techniques in which a fogged emulsion or an internally fogged emulsion is utilized. Further, Japanese Patent O.P.I. Publication No. 51941-1976 discloses a hydroquinone derivative capable of releasing an organic inhibitor. In the above-given techniques on the whole, an IIE control is attempted in the primary developing step, however, a satisfactory effect has not always been achieved, because the above-mentioned means has generally little effect on an attempt to increase an IIE in the primary developing step, i.e., the black-and-white development step of a color reversal process and the means has further raised the problems of various bad influences such as a faulty desalting which is apt to occur when a silver iodide content is increased and stains which is produced in the secondary development step.
On the other hand, there has been a well-known attempt that an interlayer effect is tried to be produced in a color developing step, i.e., in the secondary developing step of a reversal process. Japanese Patent O.P.I. Publication No. 84646-1986, for example, discloses a technique in which an IIE is obtained by diffusing scavengers for the oxidized products of a color developing agent from one layer into the other layers so that the color density of the layers may be regulated. This technique has many passive advantages because the primary development is not seriously affected, however, the positive effects thereof are not so noticeable. Therefore, a technique capable of increasing an IIE has so far been demanded for.
Meanwhile, gradation may be regarded as an essential factor exerting an influence upon the image quality of silver halide reversal light-sensitive materials. In silver halide reversal light-sensitive materials, such gradation may be controlled mainly by changing the characteristics of silver halide grains. Namely, an aimed gradation may be obtained by controlling the iodide contents of silver halides or by mixing plural silver halides which are different in grain size and sensitivity. However, these techniques have not been satisfactory, because not only any great effect has not been expectable in general, but also many problems have been raised, such as a faulty desalting which is apt to occur when a silver iodide content is increased and a graininess deterioration which is apt to occur when a grain size is enlarged.
There is also a well-known means in which a gradation may be adjusted by making use of two silver halide emulsion layers each different in speed. In this means, however, an IIE has been apt to further decrease, while an aimed gradation has readily been obtainable and both of color reproduction and gradation have been very hardly compatible with each other.
SUMMARY OF THE INVENTION
In order to solve the above-mentioned problems, an object of the invention is to provide a silver halide reversal light-sensitive material excellent in both color reproduction and gradation.
The above-mentioned object of the invention can be accomplished with a silver halide reversal photographic light-sensitive material comprising a support having thereon a photographic component layers including at least two silver halide layers, at least one of which comprises of at least two silver halide emulsion layers each having substantially the same color sensitivity and different in speed, and a DIR layer which does not substantially contribute for any image formation and contains a DIR compound and a silver halide emulsion.

DETAILED DESCRIPTION OF THE INVENTION
Now, the invention will be described in more detail.
At least two silver halide emulsion layers of the invention each different in speed are comprised of a plurality of silver halide emulsion layers each having substantially the same color-sensitivity and the different speed. The meaning of the expression, `substantially the same color-sensitivity`, includes that, the color-sensitivity of light-sensitive layers are regarded as substantially the same even when both of the light-sensitive regions are slightly different each other in one and the same wavelength range, that is, even when the two spectral sensitivities are slightly different each other, provided that the light-sensitive layers have a light-sensitivity to a certain spectral wavelength region such as either one of blue-, green- and red-regions of an ordinary type multilayered color light-sensitive material.
When a light-sensitive layer having the same color-sensitivity is comprisedof two layers each different in speed, it is preferred that a higher speed silver halide emulsion layer and a lower speed silver halide emulsion layer should be arranged in order from the side far from a support. When it is comprised of three or more layers, it is similarly preferred that the silver halide emulsion layers should be arranged in order of those having more higher speed and from the side far from the support.
When the light-sensitive layer is comprised of two layers, the optimum speed difference between or among the higher and lower speed silver halideemulsion layers may be obtained in a commonly known method, taking a gradation and so forth into consideration. Usually, the difference thereofis preferably from 0.2 to 1.5 and, more preferably, from 0.3 to 1.0, each in terms of .DELTA.log E, (in which E represents an exposure). Such .DELTA.log E value may be adjusted to an optimum value in accordance with silver halide emulsion grain sizes, chemical ripening degrees and the amounts of inhibitors added. The density proportion of image formed by thehigher speed silver halide emulsion layer to image formed by the lower speed silver halide emulsion layer is preferably within the range of from 10:90 to 90:10 and, more preferably, from 25:75 to 75:25.
Also, when the light-sensitive layer having the same color-sensitivity is comprised of three or more layers, an optimum value thereof may be obtained in the same way as mentioned above.
The silver halide emulsions relating to the invention are allowed to use therein silver bromide, silver iodobromide, silver chloride and silver chloroiodobromide. A preferable silver chloride content is from 0 mol % to90 mol % and, more preferably, from 0 to 50 mol %.
The silver halide emulsions relating to the invention are allowed to contain silver iodide. A silver iodide content is preferably not more than20 mol %, more preferably not more than 12 mol % and, particularly from 0 to 6 mol %.
It is preferred that the rest of the compositions of the silver halide emulsions relating to the invention should be silver bromide.
It is also preferred that the silver halide emulsions relating to the invention should be monodispersed. In the invention, the monodispersed silver halide emulsions contain silver halides having the grain sizes within the range of +20% with respect to the average grain size d thereof in an amount of preferably not less than 60% by weight of the amount by weight of the whole silver halide grains, more preferably not less than 70% by weight and, partucularly not less than 80% by weight. An average grain size d mentioned herein is defined as a grain size di obtained when a product ni x di.sup.3 of a frequency ni of grains having a grain size diand di.sup.3, in which the significant digits are three and the fractions of 5 and over are counted as a unit and the rest is disregarded.
The term, `grain size`, mentioned herein means a grain diameter when silverhalide grains are spherical-shaped, or a diameter of a circular image having the same area as that of the projective image of the grain when silver halide grains are other than spherical-shaped.
Grain sizes ma be measured in such a manner that they are photographed after they are magnified ten thousand to fifty thousand times by an electron microscope and the diameters of the grains or the projective areas thereof are measured on the printed photograph, (provided that the numbers of the grains to be measured are indiscriminately not less than one thousand.)
When a grain size distribution (%) is defined by the following formula. ##EQU1##the grain size distribution of the particularly preferable highly monodispersed emulsions of the invention should be not more than 20%, provided herein that an average grain size and a standard deviation are tobe obtained from the above-defined di.
Such monodispersed emulsions may be obtained in such a manner that a water-soluble silver salt solution and a water-soluble halide solution areadded into a gelatin solution containing seed grains, under the control of pAg and pH, in a double-jet process. The particularly preferable preparingprocesses may be referred to Japanese Patent O.P.I. Publication No. 46640-1984.
An average grain size d of the silver halide emulsions of the invention should be within the range of, preferably, from 0.05 to 10.0 .mu.m and, more preferably, from 0.1 to 5.0 .mu.m.
In the silver halide emulsions of the invention, the silver halide grains thereof are allowed to have either the uniform distribution of a halide composition, or the different halide compositions between the inside and outside of grains i.e., the so-called core/shell type grains.
The silver halide emulsions of the invention are also allowed to have such a regular crystal form as a cube, octahedron, tetradecahedron and so forth. In these grains, any ratio of a (100) plane to a (111) plane may beapplied and it is further allowed to mix any other grains having a variety of crystal forms therein.
The silver halide emulsions applicable to the invention may also be the mixtures of two or more kinds of silver halide emulsions each separately prepared.
Silver halide grains applicable to the silver halide emulsions of the invention may be added therein with metal ions by making use of at least one kind of metal salts selected from the group consisting of the salts ofcadmium, zinc, lead, thallium, iridium including the complex salts thereof,rhodium including the complex salts thereof and iron including the complex salts thereof so that these metal elements may be contained in the inside and/or surfaces of the grains. It is also allowed to provide reduction-sensitization nuclei to the inside and/or surfaces of the grains, when the grains are put in an atmosphere suitable for reduction.
The silver halide emulsions of the invention may be chemically sensitized in an ordinary process. Namely, a sulfur sensitization, a selenium sensitization, a reduction-sensitization, a noble metal sensitization using gold or other noble metal compounds and so forth may be used independently or in combination.
The silver halide emulsions of the invention may also be optically sensitized to a desired wavelength region by making use of a dye which is known as a sensitizing dye in the photographic industry. These sensitizingdyes may be used independently or in combination. The silver halide emulsions of the invention are also allowed to contain, together with the sensitizing dyes, a supersensitizer capable of enhancing the sensitizationfunction of the sensitizing dyes, that is, a dye having no spectral sensitizing function in itself or a compound incapable of substantially absorbing any visual rays of light.
Now, a DIR compounds which may be contained in the DIR layers of the invention will be described. Such a DIR compound may also be added into any ordinary type of silver halide emulsion layers at the same time when the DIR compounds are added into the DIR layers.
In the invention, the DIR compounds mean a compound capable of releasing either a development inhibitor or a compound capable of releasing the development inhibitor, upon reaction with the oxidized product of a color developing agent. Among these DIR compounds, a diffusible DIR compounds should be preferred.
In the invention, the diffusible DIR compounds mean a compound capable of releasing either a development inhibitor upon reaction with the oxidized product of a color developing agent or a compound capable of releasing another compound capable of releasing a development inhibitor thereupon and the diffusibility of the above development inhibited or compound capable of releasing a development inhibitor should be not less than 0.34 and, more preferably, not less than 0.40 in accordance with the evaluationmethod of which will be described later.
The diffusibility may be evaluated in the following method.
Samples (I) and (II) each of light-sensitive materials are prepared so as to comprise a transparent support bearing thereon the layers having the following composition.
Sample (I): A sample having a green-sensitive silver halide emulsion layer
This sample was prepared in the following manner.
A gelatin coating solution was so prepared as to contain silver iodobromidespectrally sensitized to green (having a silver iodide content of 6 mol % and an average grain size of 0.48 .mu.m) and the following coupler in an amount of 0.07 mols per mol of silver, and the resulted gelatin coating solution was coated so that an amount of silver coated may be 1.1 g/m.sup.2 and an amount of gelatin added may be 3.0 g/m.sup.2. Further, toserve as a protective layer coated thereon, another gelatin coating solution containing silver iodobromide neither chemically nor spectrally sensitized (having a silver iodide content of 2 mol % and an average grainsize of 0.08 .mu.m) was coated so that an amount of silver coated may be 0.1 g/m.sup.2 and an amount of gelatin added may be 0.8 g/m.sup.2. ##STR1##
Sample (II): Sample prepared by eliminating silver iodobromide from the protective layer of the above-mentioned Sample (I)
To each of the layers, a gelatin hardener and a surface active agent were added, besides the above-given materials.
The samples (I) and (II) were exposed to white light through a an optical wedge and were then treated in the following processing steps. As for the developers, there used one added with various development inhibitors in anamount capable of inhibiting the light-sensitivity of Sample (II) to 60% (that is, -.DELTA.log E=0.22 in logarithmic terms) and the other not addedwith any development inhibitor.
______________________________________Processing steps (at 38.degree. C.)______________________________________Color developing 2 min. 40 sec.Bleaching 6 min. 30 sec.Washing 3 min. 15 sec.Fixing 6 min. 30 sec.Washing 3 min. 15 sec.Stabilizing 1 min. 30 sec.Drying______________________________________
The composition of the processing solutions used in the above-mentioned processing steps were as follows.
______________________________________[Color developer]4-amino-3-methyl-N-ethyl-N-(.beta.- 4.75 ghydroxyethyl)aniline sulfateSodium sulfite, anhydrous 4.25 gHydroxylamine 1/2 sulfate 2.0 gPotassium carbonate, anhydrous 37.5 gPotassium bromide 1.3 gtrisodium nitrilotriacetate monohydrate 2.5 gPotassium hydroxide 1.0 gAdd water to make 1 liter[Bleaching solution]Ferric-ammonium ethylenediamine- 100.0 gtetraacetateDiammonium ethylenediaminetetraacetate 10.0 gAmmonium bromide 150.0 gGlacial acetic acid 10.0 mlAdd water to make 1 literAdjust pH with aqueous ammonia to pH = 6.0[Fixer]Ammonium thiosulfate 175.0 gSodium sulfite, anhydrous 8.5 gSodium metasulfite 2.3 gAdd water to make 1 literAdjust pH with acetic acid to pH = 6.0[Stabilizer]Formalin (a 37% aqueous solution) 1.5 mlKoniducks (Manufactured by Konishiroku 7.5 mlPhoto Ind. Co., Ltd.)Add water to make 1 liter______________________________________
Desensitization degree of Sample (I) is represented by the following formula:
.DELTA.S=S.sub.0 -S.sub.I,
Desensitization degree of Sample (II) is represented by the following formula:
.DELTA.S.sub.0 =S.sub.0 -S.sub.II, and
Diffusibility=.DELTA.S/.DELTA.S.sub.0,
wherein S.sub.0 represents a sensitivity of Sample (I) obtained when no development inhibitor was added; S.sub.0, represents a sensitivity of Sample (II); S represents a sensitivity of Sample (I) obtained when a development inhibitor was added; and S.sub.II represents a sensitivity of Sample (II); provided that every sensitivity are indicated by the logarithm (-log E) of the reciprocal of an exposure obtained at the point of a fog density+a density of 0.3.
According to the above mentioned method, the diffusibility of several kindsof development inhibitors were obtained. The results thereof are shown in the table given below.
TABLE__________________________________________________________________________ Amt. added Desensitization DiffusibilityStructure (Mol/liter) .DELTA.S.sub.0 .DELTA.S .DELTA.S/.DELTA.S.sub.0__________________________________________________________________________ ##STR2## 1.3 .times. 10.sup.-5 0.22 0.05 0.23 ##STR3## 1.3 .times. 10.sup.-5 0.23 0.08 0.34 ##STR4## 2.5 .times. 10.sup.-5 0.22 0.10 0.45 ##STR5## 3.0 .times. 10.sup.-5 0.21 0.10 0.48 ##STR6## 1.4 .times. 10.sup.-5 0.23 0.11 0.48 ##STR7## 2.5 .times. 10.sup.-5 0.22 0.13 0.59 ##STR8## 3.5 .times. 10.sup.-5 0.23 0.15 0.65 ##STR9## 4.3 .times. 10.sup.-5 0.22 0.16 0.73 ##STR10## 1.7 .times. 10.sup.-5 0.21 0.20 0.95__________________________________________________________________________
In the DIR compounds of the invention, the diffusibility of the groups released therefrom should preferably be within the above-given range, however, any one other than the above may also be used.
Typical formulas thereof will be given below.
Formula (D-1)
A-(Y)m
wherein A represent a coupler residue and Y is a development inhibiting group or a group capable of releasing a development inhibiting group, in which said group represented by Y is bonded in the coupling position of the coupler residue represented by A and capable of being split off from said coupler residue upon reaction of with the oxidized product of a colordeveloping agent, and m represent an integer of 1 or 2.
In the above-given Formula (D-1), Y may typically be presented by the following Formulas (D-2) through (D-9). ##STR11##
In the above-given formulas (D-2) through (D-7), Rd.sub.1 represents a hydrogen atom, a halogen atom, or a group of alkyl, alkoxy, acylamino, alkoxycarbonyl, thiazolidinylideneamino, aryloxycarbonyl, acyloxy, carbamoyl, N-alkylcarbamoyl, N,N-dialkylcarbamoyl, nitro, amino, N-arylcarbamoyloxy, sulfamoyl, N-alkylcarbamoyloxy, hydroxy, alkoxycarbonylamino, alkylthio, arylthio, aryl, heterocyclic, cyano, alkylsulfonyl or aryloxycarbonylamino, respectively; n is an integer of 0,1or 2, provided that, when n is 2, each of Rd.sub.1 s may be the same with or different from each other; and a total number of carbon atoms containedin n of Rd.sub.1 s is from 0 to 10; and, in Formula (D-6). the number of the carbon atoms contained in Rd.sub.1 is preferably from 0 to 15.
In the above-given Formula (D-6), X represents an oxygen atom or a sulfur atom.
In the above-given Formula (D-8), Rd.sub.2 represents an alkyl group, an aryl group or a heterocyclic group.
In the above-given Formula (D-9), Rd.sub.3 represents a hydrogen atom or a group of alkyl, cycloalkyl, aryl or heterocyclic, respectively: and Rd.sub.4 represents a hydrogen atom, a halogen atom or a group of alkyl, cycloalkyl, aryl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, alkanesulfonamido, cyano, heterocyclic, alkylthio or amino, respectively.
When Rd.sub.1, Rd.sub.2, Rd.sub.3 or Rd.sub.4 represents an alkyl group, such alkyl groups include those each having a substituent and they may be straight-chained or branched.
When Rd.sub.1, Rd.sub.2, Rd.sub.3 or Rd.sub.4 represents an aryl group, such aryl groups include those each having a substituent.
When Rd.sub.1, Rd.sub.2, Rd.sub.3 or Rd.sub.4 represents a heterocyclic group, such heterocyclic groups include those each having a substituent and the preferable hetero atoms thereof should include those each having a5- or 6-member single or condensed ring containing at least one atom selected from the group consisting of nitrogen atom, oxygen atom and sulfur atom. For example, these hetero atoms may be selected from each group of pyridyl, quinolyl, furyl, benzothiazolyl, oxazolyl, imidazolyl, thiazolyl, triazolyl, benzotriazolyl, imido, oxazine and so forth.
In the above-given Formulas (D-6) and (D-8), the number of carbon atoms contained in Rd.sub.2 is from 0 to 15.
In the above-given Formula (D-9), a total number of carbon atoms contained in Rd.sub.3 and Rd.sub.4 is preferably from 0 to 15.
Formula (D-10)
-TIME-INHIBIT
wherein TIME represents a group capable of being cleft upon reation with the oxidized product of a color developing agent and releasing an INHIBIT group with a suitable control after it is cleft from a coupler; and INHIBIT represents a group capable of serving as a development inhibitor through the above-mentioned releasing, such as the groups represented by the above-given Formulas (D-2) through (D-9).
In the above-given Formula (D-10), the -TIME-INHIBIT-group may typically berepresented by the following Formulas (D-11) through (D-19). ##STR12##
In the above-given Formulas (D-11) through (D-15) and (D-18), Rd.sub.5 represents a hydrogen atom, a halogen atom or a group of alkyl, cycloalkyl, alkenyl, aralkyl, alkoxy, alkoxycarbonyl, anilino, acylamino, ureido, cyano, nitro, sulfonamido, sulfamoyl, carbamoyl, aryl, carboxy, sulfo, hydroxy or alkanesulfonyl, respectively. In the Formulas (D-11) through (D-13). (D-15) and (D-18), Rd.sub.5 s may be coupled to each otherso as to complete a condensed ring. In the Formulas (D-11), (D-14), (D-15) and (D-19), Rd.sub.6 represents a group of alkyl, alkenyl, aralkyl, cycloalkyl, heterocyclic or aryl, respectively. In the Formulas (D-16) and(D-17), Rd.sub.7 represents a hydrogen atom or a group of alkyl, alkenyl, aralkyl, cycloalkyl, heterocyclic or aryl, respectively. In the above-given Formula (D-19), Rd.sub.8 and Rd.sub.9 each represent a hydrogen atom or an alkyl group including preferably those having 1 to 4 carbon atoms. In the Formulas (D-11) through (D-13), (D-15), and (D-18), kis an integer of 0, 1 or 2. In the Formulas (D-11) through (D-13), (D-15) and (D-18), is an integer of 1 to 4. In the Formula (D-16), m is an integer of 1 or 2, provided that, when m is 2, each of Rd.sub.7 s may be the same with or different from each other. In the Formula (D-19), n is aninteger of 2 to 4, provided that n of Rd.sub.8 and Rd.sub.9 may be the samewith or different from each other. In the Formulas (D-16) through (D-18), Brepresents an oxygen atom or ##STR13##(in which Rd.sub.6 is synonymous with the afore-defined. In the above-givenFormula (D-16), represents that a bonding may be either a single bond or a double bond, provided that m is 2 in the case of a single bond and m is 1 in the case of a double bond, and an INHIBIT group is synonymous withthose defined in the Formulas (D-2) through (D-9), except the number of carbon atoms is different.
In the INHIBIT groups, the total number of carbon atoms contained in Rd.sub.1 in a molecule in the Formulas (D-2) through (D-7) is 0 to 32; thetoal number of carbon atoms contained in Rd.sub.2 in a molecule in the Formula (D-8) is 1 to 32: and the total number of carbon atoms contained in Rd.sub.3 and Rd.sub.4 in the Formula (D-9) is 0 to 32.
Among the DIR compounds, the preferable ones are those having Y representedby Formula (D-2), (D-3) or (D-10). Among those represented by Formula (D-10), the preferable ones are those having an INHIBIT group represented by Formula (D-2) or (D-6) and more preferably (D-6) in which X represents an oxygen atom, or (D-8) and more preferably the Rd.sub.2 represents a hydroxyaryl group or an alkyl group having 1 to 3 carbon atoms.
In Formula (D-1), the coupler components represented by A include, for example, a yellow dye image forming coupler residual group, a magenta dye image forming coupler residual group, a cyan dye image forming coupler residual group and a non-dye forming coupler residual group.
The diffusible DIR compounds which should preferably be used in the invention include, for example, the following compounds. It is however to be understood that the invention shall not be limited thereto. ##STR14##
______________________________________Exemplifiedcompound No. R.sub.1 R.sub.2 Y______________________________________D-2 (1) (1) (30)D-3 (2) (3) (30)D-4 (2) (4) (30)D-5 (5) (6) (31)D-6 (2) (4) (32)D-7 (2) (3) (32)D-8 (7) (8) (33)D-33 (2) (4) (55) ##STR15##D-9 (9) (10) (30)D-10 (11) (10) (30)D-11 (12) (7) (34)D-12 (12) (13) (35)D-13 (9) (14) (36)D-14 (15) (16) (37)D-35 (56) (24) (23) ##STR16##D-15 (17) (38)D-16 (17) (39)D-17 (18) (40)D-18 (19) (41)D-19 (18) (42)D-20 (18) (43)D-21 (18) (44)D-22 (18) (45)D-23 (18) (46)D-24 (20) (47)D-25 (20) (48)D-26 (21) (49)D-27 (21) (50)D-28 (21) (51)D-29 (22) (52)D-30 (18) (53)D-31 (18) (54)D-32 (22) (49)D-34 (18) (56)______________________________________ ##STR17##
The typical examples of the DIR compounds including the above-given exemplified compounds each applicable to the invention are described in U.S. Pat. Nos. 4,234,678, 3,227,554, 3,617,291, 3,958,993, 4,149,886 and 3,933,500: Japanese Patent O.P.I. Publication Nos. 56837-1982 and 13239-1976; U.S. Pat. Nos. 2,072,363and 2,070,266; Research Disclosure No.21,228, December, 1981; and so forth.
In the invention, the term, an `DIR layer`, means a layer containing a DIR compound and a light-sensitive silver halide emulsion, which does not formany substantial color image. The expression, a DIR layer does `not form anysubstantial color image`, means that the layer has a maximum density of notmore than 0.3 after developed, preferably not more than 0.2 and more preferably not more than 0.1 in terms of either a transmission density in the case of a transmission type photographic material or a reflection density in the case of a reflection type photographic material. Any light-sensitive silver halides may be used in the DIR layers, such as silver chloride, silver bromide, silver iodide, silver chlorobromide, silver iodobromide, or silver chloroiodobromide. The grain size thereof may be from 0.05 to 2 .mu.m and should preferably be from 0.1 to 1.5 .mu.m. The amount of such silver halides coated may be from 0.01 g/m.sup.2to 3.0 g/m.sup.2 and should preferably be from 0.05 g/m.sup.2 to 1.5 g/m.sup.2.
In the invention, there is no special limitation to the positions of the DIR layers. It is, however, preferred to arrange them to the neighborhood of a silver halide emulsion layer comprising at least two layers each having substantially the same color sensitivities which are different fromthe color sensitivity of the silver halides of the DIR layers. To be more concrete, for example, that may be the case that, in the case of trying toimprove a red color reproducibility, a green- or blue-sensitive DIR layer, or a DIR layer containing both of a green-sensitive silver halide and a blue-sensitive silver halide should preferably be arranged to the neighborhood of a red-sensitive silver halide emulsion layer comprising atleast two layers. Also, in the case of improving a green- or blue-reproducibility, the same arrangements may be applied. The word, `neighborhood`, means that a DIR layer is so arranged as to be adjacent toa silver halide emulsion layer or adjacent thereto with the interposition of an interlayer. It should be preferred to arrange the DIR layer closer to the side of a support than the above-mentioned silver halide emulsion layer comprising at leat two layers. The most preferable position of the DIR layer should be a position where it is arranged much closer to the support side than the position of the above-mentioned silver halide emulsion layer comprising at least two layers. It is also allowed to arrange one or more DIR layers on the support, and in the case of using two or more DIR layers, the color sensitivity thereof should preferably bedifferent from each other.
The silver halide emulsions of the invention are allowed to contain an antifogging agent, a stabilizer and so forth. As for the binders for such emulsions, gelatin may advantageously be used.
Such emulsion layers and other hydrophilic collidal layers may be hardened and may also contain a plasticizer and a water-soluble or silver-dissolvable synthetic polymer dispersion that is so-called a latex.
In the emulsion layers of the color light-sensitive material, a coupler is used and, in addition, it is also allowed to use a competing coupler capable of displaying a color correction effect and a compound capable of releasing such a photographically useful fragment as a development accelerator, a developing agent, a fogging agent, an antifogging agent, a chemical sensitizer, a spectral sensitizer and a desensitizer, through a coupling to the oxidized product of a color developing agent.
To a light-sensitive material, it is allowed to apply such a auxiliary layer as a filter layer, an antihalation layer, an antiirradiation layer and so forth. These layers and/or emulsion layers are also allowed to contain a dyestuff which may be made effluent from the light-sensitive material or bleached, in the course of a development.
Such light-sensitive materials may also be added with a matting agent, a lubricant, an image stabilizer, a formalin scavenger, a UV absorbing agent, a fluorescent brightening agent, a surface active agent, a development accelerator and a development inhibitor.
As for the supports of the light-sensitive materials, a sheet of paer laminated with polyethylene or the like, a polyethyleneterephthalate film,a baryta paper, a cellulose triacetate film and so forth may be used.
When using the light-sensitive materials of the invention, a dye image may be obtained by exposing them to light and then carrying out a popularly known color reversal process.
Namely, a dye image may be obtained on the light-sensitive material in sucha manner that a silver halide which was exposed to light in the primary developins step is treated in a monochromatic developing step and unexposed silver halides are then fogged in either a light-fogging treatment or a fogging bath and, successively, a color development is carried out.
EXAMPLES
Some examples of the invention will now be described below. It is, however,to be understood that the invention shall not be limited thereto.
EXAMPLE 1
Color reversal light-sensitive material No. 1 was prepared in such a mannerthat the following Layer 1 through Layer 12 were coated over to a paper support laminated on the both side thereof with polyethylene. The amount of each component coated will be shown in terms of g/m.sup.2, provided that the amount of each silver halide will be shown in terms of an amount of silver used.
______________________________________Layer 1 (An antihalation layer)Black colloidal silver 0.05Gelatin 0.20Layer 2 (A green-sensitive DIR layer)Green-sensitive silver bromide emulsion(An average grain size: 0.7 .mu.m) 0.10DIR compound (D-23) 0.10Gelatin 2.0Layer 3 (The first interlayer)Gelatin 0.08Color mixing inhibitor 1.0Layer 4 (A red-sensitive layer)Cyan coupler A 0.34Cyan coupler B 0.17Red-sensitive silver iodobromide emulsion 0.20(A silver iodobromide content: 2 mol %)(An average grain size: 0.6 .mu.m)Gelatin 2.0Layer 5 (The second interlayer)Color mixing inhibitor 0.08Gelatin 1.0Layer 6 (A red-sensitive DIR layer)Red-sensitive silver bromide emulsion 0.1(An average grain size: 0.6 .mu.mGelatin 2.0DIR compound (D-23) 0.1Layer 7 (The third interlayer)Color mixing inhibitor 0.08Gelatin 1.0Layer 8 (A green-sensitive layer)Magenta coupler 0.28Green-sensitive silver iodobromide emulsion 0.10(A silver iodide content: 2 mol %)(An average grain size: 0.5 .mu.m)Green-sensitive silver iodobromide emulsion 0.20(A silver iodide content: 2 mol %)(An average grain size: 0.9 .mu.m)Gelatin 2.0Layer 9 (The fourth interlayer)Yellow colloidal layer 0.15Color mixing inhibitor 0.08Gelatin 1.0Layer 10 (A blue-sensitive layer)Yellow coupler 0.60Blue-sensitive silver iodobromide emulsion 0.15(A silver iodobromide content: 2 mol %)(An average grain size: 0.5 .mu.m)Blue-sensitive silver iodobromide emulsion 0.20(A silver iodobromide content: 2 mol %)(An average grain size: 1.0 .mu.m)Gelatin 2.0Layer 11 (A UV absorbing layer)UV absorbing agentA 0.2B 0.2C 0.2D 0.2Gelatin 2.0Layer 12 (A protective layer)Gelatin 1.0______________________________________
Besides the above, the color reversal light-sensitive material contained a high boiling solvent, an antifading agent, a surface active agent, a hardener and an antiirradiation dye.
__________________________________________________________________________Cyan coupler A ##STR18##Cyan coupler B ##STR19##Magenta coupler ##STR20##Yellow coupler ##STR21##UV absorbing agent ##STR22## R.sub.1 R.sub.2 R.sub.3__________________________________________________________________________A (t)C.sub.4 H.sub.9 (t)C.sub.4 H.sub.9 HB (t)C.sub.4 H.sub.9 CH.sub.3 ClC (t)C.sub.4 H.sub.9 (t)C.sub.4 H.sub.9 ClD (t)C.sub.5 H.sub.11 (t)C.sub.5 H.sub. 11 H__________________________________________________________________________Color mixing inhibitor ##STR23##__________________________________________________________________________
Next, Samples 2 through 4 were prepared by changing a part of the layers ofSample 1 as shown in Table 1.
TABLE 1______________________________________Sample No. Point of change Remarks______________________________________Sample 2 In place of the 4th layer of Sample 1, Invention Layers 4a and the following Layer 4b were arranged in order from the support side.Sample 3 DIR compound and silver halides of Out of the both 2nd and 6th layers of Sample 2 invention were eliminated.Sample 4 DIR compound (D-23) of 0.02 mol/mol Out of the Ag was added to Layers 4a, 4b and 8 of invention Sample 3, respectively.Layer 4a: The first red-sensitive layer Cyan coupler A 0.14 Cyan coupler B 0.07 Red-sensitive silver iodobromide emulsion (A silver iodide content: 2 mol %) 0.14 (An average grain size: 0.4 .mu.m) Gelatin 1.0Layer 4b: The second red-sensitive layer Cyan coupler A 0.20 Cyan coupler B 0.10 Red-sensitive silver iodobromide emulsion (A silver iodide content: 2 mol %) 0.16 (An average grain size: 0.6 .mu.m) Gelatin 1.0______________________________________
The above-mentioned light-sensitive materials 1 through 4 were exposed to white light (Exposure B) and red light (Exposure A, through a CC-90R filter manufactured by Eastman Kodak Co.) and were then processed in the following order.
______________________________________(Processing steps)Primary developing 1 min. 15 sec.(Monochromatic developing) (at 38.degree. C.)Washing 1 min. 30 sec.Light foggingSecondary developing 2 min. 15 sec.(Color developing) (at 38.degree. C.)Washing 45 sec.Bleach-fixing 2 min. (at 38.degree. C.)Washing 2 min. 15 sec.(Primary developer)Potassium sulfite 3.0 gSodium thiocyanate 1.0 gSodium bromide 2.4 gPotassium iodide 8.0 mgPotassium hydroxide (48%) 6.2 mlPotassium carbonate 14 gSodium hydrogencarbonate 12 g1-phenyl-4-methyl-4-hydroxymethyl-3-pyrazolidone 1.5 gHydroquinone monosulfonate 23.3 gAdd water to make 1.0 liter (pH = 9.65)(Color developer)Benzyl alcohol 14.6 mlEthylene glycol 12.6 mlPotassium carbonate, anhydrous 26 gPotassium hydroxide 1.4 gSodium sulfite 1.6 g3,6-dithiaoctane-1,8-diol 0.24 gHydroxylamine sulfate 2.6 g4-N-ethyl-N-.beta.-(methanesulfonamidethyl)- 5.0 g2-methyl-p-phenylenediaminesesqui-sulfateAdd water to make 1.0 liter(Bleach-fixer)A solution containing 1.56 mol of 115 mlammonium salt of ferric ethylene-diaminetetraacetate complexSodium metabisulfite 15.4 gAmmonium thiosulfate (58%) 126 ml1,2,4-triazole-3-thiol 0.4 gAdd water to make 1.0 liter (pH = 6.5)______________________________________
The red light reflection density of each processed sample was measured, andthe results thereof are shown in Table 2 below.
TABLE 2______________________________________Sample Red-light reflection density*.sup.1No. Exposure A Exposure B Latitude*.sup.2______________________________________1 0.65 0.80 1.62 0.45 0.85 2.73 1.0 1.0 1.9 (Standard)4 0.75 0.65 1.3______________________________________*.sup.1 Red-light reflection densitied were obtained when a sample was exposed to redlight, Exp. A, or whitelight, Exp. B. Quantities of the exposures were the same as required to obtain a density 1.0 in Sample 3.*.sup.2 In a cyan image obtained by exposing to white light, a length of the straightline portion thereof is expressed in terms of log E.
As is obvious from Table 2, it is found that Sample 2 of the invention was the lowest in cyan density obtained when exposing it to red-light as compared to the cyan density obtained when exposing it to white-light, so that a color reproduction having a higher purity can be obtained. It is also found that the latitude obtained when exposing to white-light was thewidest. When the green-sensitive layer of Sample 1 was double-layered and the modified sample was exposed to red-light and white-light and was then evaluated, the similar results were obtained.
Also, when the DIR compounds were replaced by D-6, D-17 and D-27, the same effects were obtained, respectively.
EXAMPLE 2
In this example, the amounts of sensitizing dyes and couplers added will beexpressed in an amount per mol of silver halides used, unless otherwise expressly stated.
Sample 5 of a multilayered color light-sensitive material was prepared by coating over to a subbed triacetyl cellulose film support with the layers having the following composition in order from the support side.
______________________________________Layer 1: An antihalation layerUV absorbing agent-1 0.3 g/m.sup.2UV absorbing agent-2 0.4 g/m.sup.2Black colloidal silver 0.24 g/m.sup.2Gelatin 2.7 g/m.sup.2Layer 2: An interlayer2,5-di-t-octyl hydroquinone 0.1 g/m.sup.2Gelatin 1.0 g/m.sup.2Layer 3: A low-speed red-sensitive silverhalide emulsion layerAgBrI emulsion (Emulsion-1 0.5 g/m.sup.2(An AgI content: 2.5 mol %) (in terms(An average grain size (.sup.-- .gamma.): 0.35 .mu.m) of silver)Sensitizing dye-1 7.6 .times. 10.sup.-4 molCoupler C-1 0.1 molGelatin 0.9 g/m.sup.2Layer 4: A high-speed red-sensitive silverhalide emulsion layerAgBrI emulsion (Emulsion-2) 0.8 g/m.sup.2(An AgI content: 2.5 .mu.m) (In terms(An average grain size (.sup.-- .gamma.): 0.75 .mu.m) of silver)Sensitizing dye-1 3.2 .times. 10.sup.-4 molCoupler C-1 0.2 molGelatin 1.75 g/m.sup.2Layer 5: An interlayer2,5-di-t-octyl hydroquinone 0.1 g/m.sup.2Gelatin 0.9 g/m.sup.2Layer 6: A low-speed green-sensitive silverhalide emulsion layerEmulsion-1 (In terms of silver) 1.0 g/m.sup.2Sensitizing dye-2 6.6 .times. 10.sup.-4 molSensitizing dye-3 0.6 .times. 10.sup.-4 molCoupler M-1 0.05 molGelatin 0.8 g/m.sup.2Layer 7: A high-speed green-sensitive silverhalide emulsion layerEmulsion-2 (In terms of silver) 1.0 g/m.sup.2Sensitizing dye-2 2.76 .times. 10.sup.-4 molSensitizing dye-3 0.23 .times. 10.sup.-4 molCoupler M-1 0.15 molGelatin 1.5 g/m.sup.2Layer 8: An interlayerThe same as Layer 5Layer 9: A yellow filter layerYellow colloidal silver 0.1 g/m.sup.2Gelatin 0.9 g/m.sup.22,5-di-t-octyl hydroquinone 0.1 g/m.sup.2Layer 10: A low-speed blue-sensitive silverhalide emulsion layerAgBrI emulsion (Emulsion-3) 0.4 g/m.sup.2(An AgI content: 2.5 mol %) (In terms(An average grain size (.sup.-- .gamma.): 0.6 .mu.m) of silver)Coupler Y-1 0.3 molGelatin 1.3 g/m.sup.2Layer 11: A high-speed blue-sensitive silverhalide emulsion layerAgBrI emulsion (Emulsion-4) 0.8 g/m.sup.2An AgI content: 2.5 mol %) (In termsAn average grain size (.sup.-- .gamma.): 1.0 .mu.m) of silver)Coupler Y-1 0.3 molGelatin 2.1 g/m.sup.2Layer 12: The first protective layerUV absorbing agent-1 0.3 g/m.sup.2UV absorbing agent-2 0.4 g/m.sup.2Gelatin 1.2 g/m.sup.22.5-di-t-octyl hydroquinone 0.1 g/m.sup.2Layer 13: The second protective layerNon-light-sensitive fine grainedAgBrI emulsion (In terms of silver) 0.3 g/m.sup.2(An AgI content: 1 mol %)(An average grain size (.sup.-- .gamma.): 0.08 .mu.m)Surface active agent comprisingpolymethylmethacrylate grains(Grain size: 1.5 .mu.m)Gelatin 0.7 g/m.sup.2______________________________________
Besides the above-given compositions, a gelatin hardener-1 and a surface active agent-1 were also added to each layer.
Further, tricresyl phosphate was used to serve as the solvent for the couplers. ##STR24##
Next, Samples 6 through 8 were prepared by changing a part of the layers ofSample 5 as shown in Table 3 below.
TABLE 3______________________________________Sample No. Point of change Remarks______________________________________5 Out of the invention6 In Sample 5, Layers 6 and 7 Out of the were eliminated from their invention positions and whereto the following Layer a was arranged.7 In Sample 5, the following Layer Invention b was interposed between Layers 1 and 2. The following layers c and d were interposed between Layers 5 and 6 in order from the side of Layer 5.8 In Sample 5, Layers 4 and 7 Out of the each were added with 0.04 mol invention of D-2, respectively.Layer a: Emulsion-1 1.0 g/m.sup.2 Emulsion-2 1.0 g/m.sup.2 Sensitizing dye-2 9.36 .times. 10.sup.-4 mol Sensitizing dye-3 0.83 .times. 10.sup.-4 mol Coupler M-1 0.2 mol Gelatin 2.3 g/m.sup.2Layer b: A green-sensitive DIR layer Green-sensitive silver bromide 0.1 g/m.sup.2 emulsion (An average grain size: 0.7 .mu.m) DIR compound (D-2) 0.1 g/m.sup.2 Gelatin 1.5 g/m.sup.2Layer c: A red-sensitive DIR layer Red-sensitive silver bromide 0.1 g/m.sup.2 emulsion (An average grain size: 0.6 .mu.m) DIR compound (D-2) 0.1 g/m.sup.2 Gelatin 1.5 g/m.sup.2Layer d: An interlayer The same as Layer 5______________________________________
Thus prepared Samples 5 through 8 were wedge-exposed to white-light and magenta-light through a CC-90M filter manufactured by Eastman Kodak Co. and were then processed in the following steps, respectively.
______________________________________Processing step Time Temperature______________________________________Primary developing 6 min. 38.degree. C. .+-. 0.3.degree. C.Washing 2 min. 38.degree. C. .+-. 0.3.degree. C.Reversing 2 min. 38.degree. C. .+-. 0.3.degree. C.Coor developing 6 min. 38.degree. C. .+-. 0.3.degree. C.Adjusting 2 min. 38.degree. C. .+-. 0.3.degree. C.Bleaching 6 min. 38.degree. C. .+-. 0.3.degree. C.Fixing 4 min. 38.degree. C. .+-. 0.3.degree. C.Washing 4 min. 38.degree. C. .+-. 0.3.degree. C.Stabilizing 1 min. ordinary temperatureDrying______________________________________
In the above processing steps, the following processing solutions were used.
______________________________________Primary developerSodium tetrapolyphosphate 2 gSodium sulfite 20 gHydroquinone, monosulfonate 30 gSodium carbonate, monohydrate 30 g1-phenyl-4-methyl-4-hydroxymethyl- 2 g3-pyrazolidonePotassium bromide 2.5 gPotassium thiocyanate 1.2 gPotassium iodide (A 0.1% solution) 2 mlAdd water to make 1000 mlReversal solutionsodium nitrilotrimethylenephosphonate 3 gStannous chloride, dihydrate 1 gp-aminophenol 0.1 gSodium hydroxide 8 gGlacial acetic acid 15 mlAdd water to make 1000 mlColor developerSodium tetrapolyphosphate 2 gSodium sulfite 7 gSodium tertiary phosphate, dihydrate 36 gPotassium bromide 1 gPotassium iodide (A 0.1% solution) 90 mlSodium hydroxide 3 gCitrazinic acid 1.5 gN-ethyl-N-.beta.-methanesulfonamidethyl- 11 g3-methyl-4-aminoaniline sulfate2,2-ethylenedithiodiethanol 1 gAdd water to make 1000 mlModerating solutionSodium sulfite 12 gSodium ethylenediaminetetraacetate, 8 gdihydrateThioglycerol 0.4 mlGlacial acetic acid 3 mlAdd water to make 1000 mlBleaching solutionSodium ethylenediaminetetraacetate, 2 gdihydrateFerric-ammonium ethylenediamine- 120 gtetraacetate, dihydratePotassium bromide 100 gAdd water to make 1000 mlFixing solutionAmmonium thiosulfate 80 gSodium sulfite 5 gSodium bisulfite 5 gAdd water to make 1000 mlStabilizerFormalin (37% by weight) 5 mlKoniducks (manufactured by Konishiroku 5 mlPhoto Ind. Co., Ltd.)Add water to make 1000 ml______________________________________
The yellow, magenta and cyan densities of each sample processed as above were measured by making use of an X-RITE densitometer in Status-A in such a manner that the yellow and cyan densities of each sample were measured when the magenta density of each sample was at 1.5. The results thereof are shown collectively in Table 4 below.
TABLE 4______________________________________ In-magenta- LatitudeSample exposed area in white-exposed areaNo. Yellow Cyan .DELTA.log E Linearity*______________________________________5 0.69 1.20 2.10 Fair6 0.56 1.12 1.40 Poor7 0.47 0.46 2.35 Good8 0.60 0.85 1.80 Poor______________________________________*= .DELTA.log E: A log E value of D = 0.2 and a log E value of (Dmax - 0.2) in a magenta imageLatitude: The linearity of a characteristic curve
As is obvious from Table 4, it is understood that, in Sample 7 of the invention, yellow and cyan color developments were inhibited when the sample was exposed to magenta light so as to display a highly purified color reproduction and, at the same time, a wide latitude and an excellentlinearity were also obtained, as compared to the comparative samples.
According to the invention, a reversal silver halide excellent in color reproducibility and gradation can be provided.

Number	Name	Date
4388401	Hasebe et al.	Jun 1983
4608334	Shuto et al.	Aug 1986
4725529	Shimazaki et al.	Feb 1988
4729943	Pfaff et al.	Mar 1988

Number	Date	Country
107817	May 1984	EPX
2591355	Jun 1987	FRX
2013356	Aug 1979	GBX

Silver halide reversal photographic light-sensitive material

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Patent Abstracts of Japan vol. 10, No. 169 (P-468) [2225] Jun. 14, 1986 JP-A-61-20038; 1/28/86.
Patent Abstracts of Japan vol. 10, No. 198 (P-476) [2254] Jul. 11, 1986 JP-A-61-42656; 3/1/86.