CA1120765A - High chloride silver halide emulsion internally doped with cadmium, lead, copper, zinc or mixtures thereof - Google Patents

Abstract

INTERNALLY DOPED SURFACE SENSITIZED HIGH CHLORIDE
SILVER HALIDE EMULSIONS AND PHOTOGRAPHIC ELEMENTS AND
PROCESSES FOR THEIR PREPARATION
Abstract of the Disclosure This disclosure relates to high chloride silver halide emulsions and photographic elements containing silver halide grains which are internally doped with a divalent metal. Cadmium, lead, zinc or mixtures thereof can be employed as dopants in concentrations up to 7 X 10-5 mole/mole of silver halide.

Description

` - ~

INTERNALLY DOPED SURFACE SENSITIZED HIGH CHLORIDE
SILVER HALIDE EMULSIONS AND PHOTOGRAPHIC ELEMENTS AND
PROCESSES FOR THRIR PREPARATION
Field of the Invention This invention is directed to improved photo-graphic elements of the developing out type, to high chloride silver halide emulsions and to methods of preparing such emulsions.
Summary of the Invention and State-o~-the-Art The overwhelming ma~ority of radiation-sensitive silver halide emulsions and photographic elements are light-sensitive, and of the developing out type. That is, the emulsions and elements are rendered developable in areas where imagewise exposure to light occurs and are contacted with a developer solution to produce a visible image.
Silver bromide and silver bromoiodide emulsions have been preferentially used for higher speed imaging applications.
As compared with silver bromide and silver bromo-iodide, high chloride silver halide emulsions and photo-graphic elements o~ the developing out type offer distinct advantages in a number of respects. For example, silver chloride possesses less native sensitivity in the visible region of the spectrum than silver bromide, thereby per-mitting yellow filter layers to be omitted from multicolorphotographic elements. Further, high chloride silver halides are more soluble than silver bromide and silver bromoiodide, thereby permitting development to be achieved in shorter times. Unfortunately these advantages of high chloride silver halides have frequently not been realized in higher speed imaging applications, since the relatively higher speeds of silver bromide and silver bromoiodide have dictated their use.
This invention satisfies a long standing need in the art in providing high chloride silver halide emulsions and photographic elements of the developing out type of increased photographic speed. It has been discovered that the speed of high chloride silver halide emulsions and "~ ~ .

photographic elements of the developing out type can be unexpectedly increased by doping silver halide grains which are at least 80 mole percent silver chloride~ based on total silver halide, with very low concentrations of divalent metals. This discovery is surprising not only because of the increased photographic speeds obtained, but also because extensive prior investigations of divalent metal dopants for silver halide grains by those skilled in the art have failed to identify these advantageous emulsions and photographic elements and have impliedly and, in some instances, expli-citly taught away from this discovery.
The recognized utility for incorporating di-valent metals in silver chloride containing photographic elements has been largely directed to comparatively special-ized, nondeveloping out applications using substantiallyhigher concentrations of the divalent metals than herein employed. For example~ the most extensive use of divalent metal dopants in negative-working silver chloride emulsions has occurred in printout and direct-print photographic elements. Printout photographic elements produce a negative visible image directly upon imagewise exposure without the use of a developer. Direct-print emulsions employ a high intensity imagewise exposure followed by uniform exposure to lower intensity light--e.g., ambient lighting--to provide a visible negative image. Illustrative patents disclosing divalent metal doped silver chloride emulsions useful in printout and direct-print photographic elements as well as divalent metal concentrations are set forth below in Table I.

, :'-.. ~' ~ 11 2~ r ?

Table I
Divalent Conc.
U.S. Patent Metal (Mo~e ~) .
3,033,682 (Hunt~ Pb 0.1 - 25 3,047,392 (Scott) Cd 0.65 - 25 Pb 0.35 - 6.9 3,287,136 (Mc~ride) Pb 0.01 - 1 3,615,61~ (Krohn et al~ Cu 0.03 - 15 Pb 0.07 - 50 3,66~,100 (Hee~s et al) Pb 0.05 - 15 In still a more specialized application ~laase et al U.S.
Patent 3,709,692 teaches to use large monocrystals of ;
silver chloride as radiation particle track detectors.
The silver chloride monocrystals contain 3.5 X 10 4 to 7 X 10 3 mole percent lead and 2.5 X 10 3 to 1.4 mole per-cent cadmium. The monocrystals are flashed with high intensity light to produce a visible track.
It has been reported and demonstrated that the use of divalent metal ions in negative-working silver halide emulsions of the developing out type has the effect of decreasing the sensitivity of the emulsions to ambient light. Mueller et al U.S. Patent 2,950,972 teaches to incorporate cadmium ions in silver bromide and silver ;
bromoiodide emulsions in concentrations of at least 1 X
10 3 mole percent for the purpose of increasing X-ray and -gamma sensitivity of the emulsion. Mueller et al teaches that these small amounts of cadmium have the effect of producing a marked decrease in the sensitivity of the emul-sions to visible light. This effect is demonstrated with 3 a 30 mole percent bromide silver bromochloroiodide emul-sion by Iwaosa et al U~S. Patent 3,901,711. In Example 2 .
a silver bromochloroiodide emulsion containing 30 mole per-cent bromide and a slight amount of silver iodide is treated with strontium chloride as a metal dopant and various combinations of gold chloride and polyethylene glycol. The effect of the strontium chloride is to reduce the sensitivity of low intensity exposures of emulsions I and J as compared respectively with otherwise similar ."~ ::

emulsions G and H. Iwaosa et al teaches the use of cad-mium, zinc or lead compounds in combination with gold salts and polyalkylene oxides in order to avoid undesirable high intensity reciprocity failure. Assuming lead chloride to be employed as a divalent metal salt, this requires a minimum of 3.6 X 10 3 mole percent lead to be present in the emulsion. Cadmium and zinc, being of lower molecular weight, would be present in even higher molar concentra-tions.
Halwig U.K. Patent 1,121,496 teaches to obtain higher printing speeds and wider exposure latitudes for silver chlorobromide emulsions containing at least 50 mole percent chloride by incorporating at least 0.1 gram of di-valent cadmium per mole of silver halide (i.e., 8.9 X 10 2 mole percent cadmium per mole of silver halide). Halwig avoids the lower divalent metal ion concentration levels taught by Mueller et al and demonstrated by Iwaosa et al to desensitize silver bromide, silver bromoiodide and 30 mole percent silver bromide silver bromochloroiodide emulsions.
In one aspect this invention is directed to a silver halide emulsion of the developing out type comprised of sensitized silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent silver iodide, based on total silver halide. The silver halide grains are internally doped with cadmium, lead, copper, zinc or mixtures thereof in a speed increasing amount of up to 7 X 10 5 mole per mole of silver halide.
In another aspect this invention is directed to a photographic element of the developing out type comprised of a support and, coated on the support, a silver halide emul-sion layer comprised of an emulsion as described above.
In an additional aspect this invention is directed to a process of forming a silver halide emulsion of the developing out type by reacting a water soluble silver salt with one or more water soluble halide salts in an aqueous medium containing a peptizer to form radiation-sensitive silver halide grains and surface chemically sensitizing the . :, ~

.
., . ' ' ,, ~
. . .

silver halide grains with a gold sensitizer. This process is characterized by the improvement comprising forming silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent silver iodide, based on total silver halide, and introducing into the aqueous medium during formation of the silver halide grains cadmium, lead, copper, zinc or mixtures thereof, in a total concentration of from 2 X 10-6 to 7 X 10-5 mole per mole of silver halide.
It has been discovered quite surprisingly that the high chloride silver halide emulsions and photographic elements containing low concentrations of divalent metal ion dopants as described above exhibit increased photographic speeds. Thus, such emulsions and photographic elements 15 offer the art recognized advantages attributable to high chloride silver halide emulsions while achieving photo-graphic speeds more commonly associated with silver bromide and silver bromoiodide photographic emulsions. The fact that the inclusion of low concentrations of divalent metal 20 ions of the type identified above can increase photographic speeds of these emulsions and photographic elements is, of course, surprising in view of the teachings in the art that low concentration levels of divalent metal ion dopants have the effect of desensitizing silver halide emulsions of 25 higher bromide concentration to visible light. By contrast, the sensitivity advantages of the emulsions and photographic elements of this invention can be realized under the exposure conditions of candid photography (that is, includ-ing low intensity and available light exposure conditions).
3 Finally, the present improvement in sensitivity has been surprisingly demonstrated to be a function of the halide content of the silver halide grains. Specifically, it has been observed that the improvement in sensitivity is highest for silver chloride, silver chlorobromides of at 35 least 80 mole percent chloride, based on total silver halide, and silver chloroiodides of less than 5 mole per-cent iodide, based on total silver halide, and that compar-able speed improvements have not been realized with silver -~
halide gralns of higher silver bromide or iodide content.
.. ~

, ~

: : . .:

.: - . ,~:: . , i , . ~ .
. .

The advantages and features of the present invention can be better appreciated by reference to the following detailed description directed to certain pre-ferred embodiments considered in conjunction with the drawings, in which Figure 1 is a plot of dopant level in mg per mole of silver versus relative speed and Figures 2 and 3 are plots of percent increase in relative speed versus mole percent silver bromide and 10 silver iodide, respectively.

The silver halide emulsions of the present inven-tion are comprised of silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole 15 percent silver iodide, based on total silver halide. In one preferred form the silver halide grains consist essentially of silver chloride. Because the solubility product constant of silver chloride is orders of magnitude ~igher than that of silver bromide or silver iodide, it is recognized that 20 formation, ripening or extended holding of silver chloride grains in the presence of bromide and/or iodide ions will result in the inclusion of silver bromide and/or silver iodide in the silver chloride grains. The preferred silver halide grains are those which are at least 30 mole percent silver chloride. The remaining silver halide, if 'any, present in the silver halide grains can be silver bromide, silver iodide or some combination of the two. Silver bromide can be present in concentrations of up to 20 mole percent, preferably up to 15 mole percent, based on total silver halide.
3 Silver iodide can be present in concentrations of less than 5 mole percent, preferably less than 2 mole percent, based on total silver halide. These silver halide grains are herein referred to as high chloride silver halide grains.
The high chloride silver halide grains contain a speed increasing amount of a metal dopant. The metal dopant can be cadmium, lead, copper, zinc or a combination of these elements in any proportion. While the metal dopants have the effect of increasing the sensitivity of , -: .
- : . . . . .
--.

sur~ace chemically sensitized high chloride silver halide grains at concentrations up to and inclucling 7 X 10 5 mole per mole of silver halide, if the concentration levels are extended upwardly, the e~fect is to desensitize the emul-sions. Significant improvements in the sensitivity of sur-face chemically sensitized emulsions have been observed when the metal dopants are introduced in concentrations in the range of from 2 X 10 6 to 7 X 10 5 mole per mole of silver halide during formation of the high chloride silver halide grains.
While cadmium, lead, zinc and copper internal dopants produce qualitatively similar effects in increasing the speed of surface chemically sensitized high chloride to silver halide emulsions, these elements differ in the de-gree to which they are capable of sensitizing the emulsions.Cadmium produces emulsions of the highest attainable sensi-tivities followed in effectiveness by zinc, lead and copper in that order. To form emulsions of the highest attainable sensitivities it is preferred to employ cadmium, zinc or combinations of these elements in concentrations of from 3 X 10-6 to 6 X 10-5, optimally 5 X 10-6 to 2.5 X 10-5, mole per mole of silver halide during formation of the high chloride silver halide grains. For emulsions of the highest attainable sensitivities using lead, copper or combinations of these elements as dopants, it is preferred to provide concentrations in the range of from 3 X 10 6 to 5 X 10 5, optimally from 8 X 10-6 to 2 X 10-5, mole per mole of silver halide during formation of the high chloride sil-ver halide grains.
3 Radiation-sensitive silver halide emulsions are conventionally formed by reacting a water soluble silver salt with one or more water soluble halide salts in an aqueous medium containing a peptizer. The choice and pro-portion of halide salts controls the halide content of the silver halide grains formed. The peptizer maintains the silver halide grains in dispersion. Where a metal dopant is intended to be introduced into the silver halide grains, it can be introduced in any convenient manner~ typically ;

;. ~,:

; ; . : : , ,. ,....... :
:

separately or with one of the sllver or halide salts or the peptizer, in the form of a salt which is water soluble in its contemplated concentration ranges. By regulating the compositions and rates of addit:Lon of halide and divalent metal salts, emulsions containing the internally doped high chloride silver halide grains described above can be pro-duced by otherwise conventional techniques~ such as the double and single jet precipitation techniques described by Mueller et al U.S. Patent 2,950,972, Iwaosa et al U.S.
Patent 3,901l711 and Halwig U.~ Patent 1,121,496.

In one preferred embodiment emulsions containing the internally doped high chloride silver halide grains described above are formed by a double Jet precipitation technique using accelerated flow rates to produce rela-tively monodispersed, cubic grains. As employed herein, the term "monodispersed" indicates that at least 95 per-cent, by weight or by number, of the silver halide grains are within 40 percent of their mean effective diameter.
In a specifically preferred form at least 95 percent, by weight or by number, of the silver halide grains are within 25 percent of the mean effective diameter, optimally within 10 percent of the mean effective diameter. The term "effective diameter" is herein employed as the diameter of the circle corresponding in area to the area subtended by a silver halide grain as viewed through a microscope or in a photomicrograph. The measurement of silver halide grain sizes is discussed further in Mees and James, The Theory of the Photograhlc Process, 3rd Ed.g Macmillan, 1966, pp. 36-43.
In double jet precipitations a silver salt, such as silver nitrate, and a chloride salt, optionally employed in combination with a bromide and/or iodide salt, such as one or more chloride or other halide salts of an alkali or alkaline earth metal te.g., sodium, potassium, magnesium or calcium), each in the form of an aqueous salt solution, are concurrently and separately introduced into the reaction vessel. An aqueous dispersing medium is present in the reaction vessel prior to the introduction of the aqueous . . . - ..

halide and silver salt solutions. The presence of the dispersing medium along with agitation, in most instances, facilitates uniform blending of the aqueous halide and silver salt solutions while avoiding localized concentration gradients. Typically a dispersing medium volume is ini-tially present in the reaction vessel which is from about 10 to 90 percent, preferably 20 to 80 percent, that of the silver halide emulsion to be formed. The dispersing medium is conventionally water or a dispersion of peptizer in water, optionally containing other ingredients, such as one or more silver halide ripening agents, more specifically described below. Preferably peptizer in a concentration of at least 10 percent, most preferably 20 percent, of the total weight of the vehicle present in the finished emulsion is initially present in the dispersing medium within the reaction vessel. Where the peptizer is not initially entire-ly present in the dispersing medium, the balance of the peptizer is preferably added during addition of the silver and halide salts. A minor portion of one of the silver or halide salt solutions, typically less than about 10 percent, is also initially present in the reaction vessel to adjust the pAg (log reciprocal silver ion concentration) of the reaction vessel contents at the outset of silver halide precipitation.
During the initial introduction of the aqueous silver and halide salt solutions into the reaction vessel the dissolved silver salt reacts with dissolved halide salt to form silver halide crystals. This initial phase of silver halide emulsion formation in which new silver halide 3 crystals are being formed is referred to as nucleation.
During subsequent addition of silver and halide salts, additional silver halide formed as a reaction product can be precipitated onto these nuclei, causing the mean size of the silver halide to increase and ultimately resulting in silver halide grains of the desired mean effective diameter.

~, , , ~ ~ . ' :, ;; ' 1', -.

:.. : ; , :, : - . , , )7~5 Although additional silver halide grain formation can occur after the initial formation of silver halide nuclei, by controlling the rate of addition of silver and halide salts continued silver halide precipitation onto the originally formed silver halide nuclei can be achieved.
This has the effect of producing a population of silver halide grains of similar size--i.e., monodispersed silver halide emulsions. Techniques are known in the art which achieve shortened silver halide precipitation times by per-mitting accelerated rates of addition of silver and halidesalts. Such techniques are disclosed, for example, by Wilgus German OLS 2,107,118 and Kurz U.S. Patent 3,672,900.

Single ~et silver halide grain precipitation is specifically contemplated as an alternative to double jet precipitation. In single ~et precipitation substantially - the entire halide salt solution is present in the reaction vessel prior to introduction of the silve~ salt solution.
The silver halide grains which are formed are polydispersed--this is, they vary significantly in size and do not satis~y the grain si~.e distribution requirements set forth above for monodispersed silver halide emulsions. Except for these differences the preferred aspects of double ~et silver halide precipitation techniques described above are also applicable ! 25 to single jet precipitation techniques.
In both the singlie jet and double ~et precipitation techniques the divalent metal salts, typically metal halides (e.g., cadmium, lead, copper and zinc chlorides), can be introduced into the reaction vessel at any time before introduction of at least 85 percent, most preferably 75 percent, of the silver salt solution has been completed.
The divalent metal salts are preferably dissolved in water or other suitable solvent prior to addition to the reaction vessel. The solution containing the divalent metal salt typically comprises from about 1 to 10 percent by weight of the dispersing medium of the emulsion, the proportions be-ing merely a matter of choice and convenience.

.' ~

:, . , .
, , ,~
~: .

7~i The individual reactants can be added to the reaction vessel through surface or sub-surface delivery tubes by gravity feed or by delivery apparatus for main-taining control of the rate of delivery and the pH and/or pAg of the reaction vessel contents, as illustrated by Culhane et al U.S. Patent 3,821,002, Oliver U.S. Patent 3,031,304 and Claes et al, Photo~raphische Korrespondenz, 102 Band, Number 10, 1967, p. 162. In order to obtain rapid distribution of the reactants within the reaction vessel, specially contructed mixing devices can be employed, as illustrated by Audran U.S. Patent 2,996,287, McCrossen et al U.S. Patent 3,342,605, Frame et al U.S.
Patent 3,415,650, Porter et al U.S. Patent 3,785,777, Saito et al German OLS 2,556,~85 and Saito et al German OLS 2,555,364. An enclosed reaction vessel can be employed to receive and mix reactants upstream of the main reaction vessel, as illustrated by Forster et al U.S. Patent 3,897,935 and Posse et al U.S. Patent 3,790,386.
The initially formed silver halide grains (i.e., silver halide nuclei~ are sufficiently small that they can be dispersed by water alone. Thus, it is unnecessary to have any peptizer initially in the reaction vessel, al-though it is frequently convenient to have the peptizer at least partially present in the reaction vessel prior to initiating introduction of the silver and halide salts.
Peptizer can be added to the reaction vessel with the halide salt, the silver salt or both and/or independently of both. While peptizer concentrations from 0.2 to about 10 percent by weight, based on the total liquid or emul-3 sion weight in the reaction vessel, can be employed, it ispreferred to keep the concentration of the peptizer in the reaction vessel prior to and during silver halide formation below about 6 percent by weight, based on the total weight. It is common practice to maintain the concentration of the peptizer in the reaction vessel in the range of from about 2 to 6 percent, based on the total weight, prior to and during silver halide formation and to adjust the emulsion vehicle concentration upwardly for llXO~i;S

optimum coating characteristics by delayed, supplemental vehicle additions. It is contemplated that the emulsion as initially formed will contain ~rom about 5 to 50 grams of peptizer per mole of silver halide, pre~erably about 5 10 to 30 grams of peptizer per mole of silver halide.
Additional vehicle can be added later to bring the con-centration up to as high as 300 grams per mole of silver halide. Preferably the concentration of vehicle in the finished emulsion is below 50 grams per mole of silver 10 halide. When coated and dried in forming a photographic J
element the vehicle preferably forms about 30 to 70 percent by weight of the emulsion layer.
Vehicles (which include both binders and peptizers) can be chosen from among those conventionally employed in 15 silver halide emulsions. Preferred peptizers are hydro-philic colloids, which can be employed alone or in combina-tion with hydrophobic materials. Suitable hydrophilic materials include both naturally occurrin~ substances such as proteins, protein derivatives, cellulose derivatives--20 e.g., cellulose esters, gelatin--e.g., alkali-treated gelatin (cattle bone or hide gelatin) or acid-treated gelatin (pigskin gelatin), gelatin derivatives--e.g., acetylated gelatin, phthalated gelatin and the like, polysaccharides such as dextran, gum arabic, zein, casein, pectin, collagen 25 derivatives, collodion, agar-agar, arrowroot, alb'umin and the like as described in Yutzy et al U.S. Patents 2,614,928 and '929, Lowe et al U.S. Patents 2,691,582, 2,614,930, '931, 2,327,808 and 2,448,534, Gates et al U.S. Patents

2,787,545 and 2,956,880, Himmelmann et al U.S. Patent

3 3,061,436, Farrell et al U.S. Patent 2,816,027, Ryan U.S.
Patents 3,132,945, 3,138,461 and 3,186,846, Dersch et al U.K. Patent 1,167,159 and U.S. Patents 2,960,405 and 3~436,220, Geary U.S. Patent 3,486,896, Gazzard U.K. Patent 793,549, Gates et al U.S. Patents 2,992,213, 3,157,506, 3,184,312 and 35 3,539,353, Miller et al U.S. Patent 3,227,571, Boyer et al U.S. Patent 3,532,50 2, Malan U.S. Patent 3,551,151, Lohmer et al U.S. Patent 4,018,609, Luciani et al U.K. Patent 1,186,790, U.K. Patent 1,489,080 and Hori et al Belgian ,: :

- ~,: : .. :

7~5 Patent 856,631, U.K. Patent 1,490,644, U.K. Patent 1,483,551, Arase et al U.K. Patent 1,459,906, Salo U.S.
Patents 2,110,491 and 2,311,086, Fallesen U.S. Patent 2,343,650, Yutzy U.S. Patent 2,322,085, Lowe U.S. Patent 2,563,791, Talbot et al U.S. Patent 2,725,293, Hilborn U.S.
Patent 2,748,022, DePauw et al U.S. Patent 2,956,883, Ritchie U.K. Patent 2,095, DeStubner U.S. Patent 1, 752, o69, Sheppard et al U.S. Patent 2,127,573, Lierg U.S. Patent 2,256,720, Gaspar U.S. Patent 2,361,936, Farmer U.K.
Patent 15,727, Stevens U.K. Patent 1,062,116 and Yamamoto et al U.S. Patent 3,923,517.
Other materials commonly employed in combination with hydrophilic colloid peptizers as vehicles including vehicle extenders--e.g., materials in the form of latices) 15 include synthetic polymeric peptizers, carriers and/or binders such as poly(vinyl lactams), acrylamide polymers, polyvinyl alcohol and its derivatives, polyvinyl acetals, polymers of alkyl and sulfoalkyl acrylates and methacrylates, hydrolyzed polyvinyl acetates, polyamides, polyvinyl pyri-20 dine, acrylic acid polymers, maleic anhydride copolymers,polyalkylene oxides, methacrylamide copolymers, polyvinyl oxazolidinones, maleic acid copolymers, vinylamine copoly-mers, methacrylic acid copolymers, acryloyloxyalkylsulfonic acid copolymers, sulfoalkylacrylamide copolymers, poly- .
25 alkyleneimine copolymers, polyamines, N,N-dialkylamino-alkyl acrylates, vinyl imidazole copolymers, vinyl sulfide :
copolymers, halogenated styrene polymers, amineacrylamide polymers, polypeptides and the like as described in Hollist-er et al U.S. Patents 3,679,425, 3,706,564 and 3,813,251, 3 Lowe U.S. Patents 2,253,078, 2,276,322, l323, 2,281,703, 2,311,058 and 2,414,207, Lowe et al U.S. Patents 2,484,456 2,541,474 and 2,632,704, Perry et al U.S. Patent 3,425,836, Smith et al U.S. Patents 3,415,653 and 3,615,624, Smith U.S. Patent 3,488,708, Whiteley et al U.S. Patents :
35 3,392,025 and 3,511,818, Fitzgerald U.S. Patents 3,681,079, 3,721,565, 3,852,073, 3,861,918 and 3,925,083, Fitzgerald et al U.S. Patent 3,879,205, Nottorf U.S. Patent 3,142,568, Houck et al U.S. Patents 3,062,674 and 3,220,844, Dann et .

~, .

;5 al U.S. Patent 2,882,161, Schupp U.S. Patent 2,579,016, Weaver U.S. Patent 2,829,053, Alles et al U.S. Patent 2,698,240, Priest et al U.S. Patent 3,oo3,879, Merrill et al U.S. Patent 3,419,397, Stonham U.S. Patent 3,284,207, Lohmer et al U.S. Patent 3,167,430, Williams U.S. Patent 2,957,767, Dawson et al U.S. Patent 2,893,867, Smith et al 3 U.S. Patents 2,860,986 and 2,904,539, Ponticello et al U.S.
Patents 3,929,482 and 3,860,428, Ponticello U.S. Patent 3,939,130, Dykstra U.S. Patent 3,411,911 and Dykstra et al 10 Canadian Patent 774,054, Ream et al U.S. Patent 3,287,289, Smith U.K. Patent 1, 466,600, Stevens U.K. Patent 1,0 62,116, Fordyce U.S. Patent 2,211,323, Martinez U.S. Patent 2,284,877, Watkins U.S. Patent 2,420,455, Jones U.S. Patent 2,533,166, Bolton U.S. Patent 2,495,918, Graves U.S. Patent 15 2,289,775, Yackel U.S. Patent 2,565,418, Unruh et al U.S.
Patents 2,865,893 and 2,875,059, Rees et al U.S. Patent 3,536,491, Broadhead et al U.K. Patent 1,348,815, Taylor et al U.S. Patent 3,479,186, Merrill et al U.S. Patent 3,520,857, Bacon et al U.S. Patent 3,690,888, Bowman U.S.
20 Patent 3,748,143, Dickinson et al U.K. Patents 808,227 and '228, Wood U.K. Patent 822,192 and Iguchi et al U.K.
Patent 1,398,055. These additional materials need not be present in the reaction vessel during silver halide pre-cipitation, but rather are conventionally added to the 25 emulsion prior to coating. The vehicle materials, includ-ing particularly the hydrophilic colloids, as well as the hydrophobic materials useful in combination therewith can be employed not only in the emulsion layers of the photo-graphic elements of this invention, but also in other 3 layers, such as overcoat layers, interlayers and layers positioned beneath the emulsion layers.
Although not required for the practice of this process, it is preferred that a silver halide ripening agent be present within the reaction vessel during silver halide formation. The ripening agent can be entirely contained within the dispersing medium in the reaction vessel before silver and halide salt addition, or it can be .

' ' ~ . , . .
:-'-37~5 introduced into the reaction vessel along with one or more of the halide salt, silver salt or peptizer. In still another variant the ripening agent can be introduced independently during halide and silver salt additions.
Sulfur containing ripening agents are generally preferred. Conventional thioether ripening agents, such as those disclosed in McBride U.S. Patent 3,271,157, can be employed. Sufficient thioether ripening agent is employed to provide concen-trations of from 0.0~ to 50 grams, preferably ab~ut 0.1 to 20 grams, per mole o~ silver h~lide, based on the weight of silver.
Certain of the preferred organic thioether silver halide solvents can be represented by the formulas:
2)r CH2-5- tCH2) 2-X- (R) - (CH ) (R' )q~S~CH2(CH2)m Z]n and Q (CH2)m (CH2 S-~H2)n-S-CH2(CH2)r_Z
wherein: r and m are integers of 0 to 4; n is an integer of 1 to 4; p and q are integers of 0 to 3; X is an oxygen atom (-O-), a sulfur atom (-S-), o a carbamyl radical ( -CNH- ), o 5 a carbonyl radical (-C-) or O
a carboxy radical (-COH);
R and R' are ethylene oxide radicals (-O-CH2CH2-); Q and ~ are hydroxy radicals (-OH), carboxy radicals, or alkoxy 3 radicals (~O-alkyl) wherein the alkyl group has 1 to 5 carbon atoms; and Q and Z can also be substituents des-cribed for X linked to form a cyclic compound.
Preferred organic thioether silver halide ripening agents suitable for forming the emulsions of the invention include compounds represented by the formulas:

- : :
-.. ,, . , ; , ~ . : :
,. .. : ~

7~5 HO(-R2-S-)rR OH, -R2-S-R2-o-R4 ) O
R3-o-R2-s_R2_cNH_R4_~2, (R3_o_R2-S-R2-)2S, ( R3-NHC-R2-S-R2- ) 2 and ~ ( R - 0) s~R~\
(R - 0) s - R2/
wherein r is an integer of l to 3; s is an integer o~ l to 2; R is an alkylene radical having l to 5 carbon atoms and is preferably ethylene (-CH~CH2-); R3 is an alkyl 15 radical having l to 5 carbon atoms and is preferably ethyl; and R is an alkylene radical having l to 5 carbon - atoms and is preferably methylene (-CH2-).
As an alternative to thioether ripening agents, thiocyanate salts can be used, such as alkali metal, most commonly potassium, and ammonium thiocyanate salts. While any conventional quantity of the thiocyanate salts can be introduced, preferred concentrations are generally from about 0.1 to 20 grams of thiocyanate salt per mole of silver halide, based on the weight of silver. Illustrative 25 pri~r teachings of employing thiocyanate ripening~agents are found in Nietz and Russell, U.S. Patent 2,222,264, -cited above; Lowe et al U.S. Patent 2,448,534, issued September 7, 1948; and Illingsworth U.S. Patent 3,320,069, issued May 16, 1967.
The emulsion containing high chloride silver halide grains is preferably washed or otherwise processed to remove soluble salts. The soluble salts can be removed by chill setting and leaching, as illustrated by Cra~t U.S.
35 Patent 2,316,845 and McFall et al U.S. Patent 3,396,~27; by coagulation washing, as illustrated by Hewitson et al U.S.
Patent 2,618,556, Yutzy et al U.S. Patent 2,614,S28, Yackel U.S.
Patent 2,565,4:18, Hart et al U.S. Patent 3,241,969, Waller - ~ ~ , ,.................. , ~, ., - . . , : :

, :. : :.: - -. :. : :

et al U.S. Patent 2~48g~341~ Klinger U.K. Patent 1,305,409 and Dersch et al U.K. Patent 1,167,159; by centrifugation and decantation of a coagulated emulsion, as illustrated by Murray U.S. Patent 2,463,794, U~ihara et al U.S. Patent 3,707,378, Audran U.S. Patent 2,996,287 and Timson U.S.
Patent 3,498,454; by employing hydrocyclones alone or in combination with centrifuges, as illustrated by U.K.
Patent 1,336,692, Claes U.K. Patent 1,356,573 and Ushomir-skii et al Soviet Chemical Industry, Vol. 6, No. 3, 1974, 10 pp. 181-185; by diafiltration with a semipermeable mem-brane, as illustrated by Research Disclosure, Vol. 102, October 1972, Item 10208, Hagemaier et al Research Dis-closure, Vol. 131, March 1975, Item 13122, Bonnet Research Disclosure, Vol. 135, July 1975, Item 13577, Berg et al 15 German OLS 2,436,461 and Bolton U.S. Patent 2,495,918 or by employing an ion exchange resin, as illustrated by Maley U.S. Patent 3,782,953 and Noble U.S. Patent 2,827,428.
The emulsions, with or without sensitizers, can be dried and stored prior to use as illustrated by Research Dis-20 closure, ~ol. 101, September 1972, Item 10152.
In order to achieve the full improvement in sen-sitivity of this invention it is preferred that the inter-nally doped high chloride silver halide grains be surface chemically sensitized. The high chloride silver halide grains can bé surface chemically sensitized with active gelatin, as illustrated by T. H. James, The Theory of the Photographic Process, 4th Ed., Macmillan, 1977, pp. 67-76, or with sulfur, selenium5 tellurium, platinum, palladium, iridium, osmium, rhenium or phosphorus sensitizers or 3 combinations of these sensitizers, such as at pAg levels of from 5 to 10, pH levels of from 5 to 8 and temperatures o~
from 30 to 80C, as illustrated by Research Disclosure, Vol.
120, April 1974, Item 12008, Research Disclosure, Vol. 134, June 1975, Item 13452, Sheppard et al U.S. Patent 1,623,499, Waller et al U.S. Patent 2~399,083, Damschroder et al U.S.
Patent 2,642,361, McVeigh U.S. Patent 3,297,447, Dunn U.S.
Patent 3,297,446, McBride U.K. Patent 1,315,755, Berry et al U.S. Patent 3,772,031, Gilman et al U.S. Patent 3,761,267, Ohi . .

,`,, ' "' ' ' ' i' ' ' ~'''' '' ~ `' :
, '~' " "' ,, ' '": ''' ' ~.

; et al U.S. Patent 3,857,711, Klinger et al U.S. Patent 3,565,633 and Oftedahl U.S. Patents 3,901,714 and 3,904,415.
The emulsions can also be reduction sensitized--e.g., with hydrogen, as illustrated by Janusonis U.S. Patent 3,891,446 and Babcock et al U.S. Patent 3,984,249, by low pAg ~e.g., less than 5) high pH ~e.g., greater than 8~ treatment or through the use of reducing agents, such as stannous chloride, thiourea dioxide, polyamines and amineboranes, as illustrated by Allen et al U.S. Patent 2,983,609, Oftedahl et al Research Disclosure, Vol. 136, August 1975, Item 13654, Lowe et al U.S. Patents 2,518,698 and 2,743,182, Chambers et al U.S. Patent 3,026,203 and Bigelow et al - U.S. Patent 3,361,564.
In a preferred form the internally doped high chloride silver halide grains are surface chemically sensi-^ tized with gold sensitizers employed alone or in combination with other conventional chemical sensitizers. The internally doped high chloride silver halide grains can be surface gold sensitized with one or a combination of con~entional 20 gold sensitizers. Illustrative gold sensitizers include gold hydroxide, gold chloride, potassium aurate, potassium auriaurite, potassium auricyanide, potassium aurithiocyanate, - gold sulfide, gold selenide, gold silver sulfide~ gold iodide, potassium chloroaurate, ethylenediamine-bis-gold chloride ~ 25 and.various organic gold sensitizers, as more fully des-; cribed by Damschroder et al U.S. Patent 2,642,361 and McVeigh U.S. Patent 3,297,447.
..
Depending upon the photographic application, . 3 emulsions containing the high chloride silver halide grains can contain other components of a conventional nature. For example3 it is specifically contemplated to blend the high chloride silver halide emulsions described above with other silver halide emulsions. Blending of silver halide emulsions is commonly undertaken to optimize characteristic curve . shapes--e.g., adjust contrast, extend exposure latitudeg increase maximum density and to achieve other, similar `~ curve modifications. Blends of surface~sensitive emulsions . . .
:, .
' ' ' . ' ' - , : : . : , .. ,, : : ~

~lZ~7~5 and internally fogged, internal image-forming emulsions can be employed, as illustrated by Luckey et al U.S. Patents 2,996,382, 3,397,987 and 3,705,858, Luckey U.S~ Patent 3,694,881, Research Disclosure, Vol. 134, June 1975, Item 13452, Millikan e~ al Defensive Publication T-904017, April 21, 1972 and Kurz Research Disclosure, Vol. 122, June 1974, Item 12233. In a specifically preferred form the maJor portion, preferably essentially all, of the sil-ver halide grains present in a silver halide emulsion or silver halide emulsion layer are internally doped high chloride silver halide grains substantially as described above.
The silver halide emulsions can be spectrally sen-sitized with dyes from a variety of classes, including the polymethine dye class, which includes the cyanines, mero-cyanines, complex cyanines and merocyanines (i.e., tri-, tetra- and poly-nuclear cyanines and merocyanines), oxonols, hemioxonols, styryls, merostyryls and streptocyanines.
The cyanine spectral sensitizing dyes include, joined by a methine linkage, two basic heterocyclic nuclei, such as those derived from quinolinium, pyridinium, iso-quinolinium, 3H-indolium, benz[e]indolium, oxazolium, thiazolium, selenazolinium, imidazolium, benzoxazolinium, benzothiazolium, benzoselenazolium, benzimidazolium, naph-thcxazolium, naphthothiazolium, naphthoselenazolium, thia-zolinium dihydronaphthothiazolium, pyrylium and imidazo-pyrazinium quaternary salts.
The merocyanine spectral sensitizing dyes include, joined by a methine linkage, a basic heterocyclic nucleus 3 of the cyanine dye type and an acidic nucleus, such as can be derived from barbituric acid, 2-thiobarbituric acid, rhodanine, hydantoin9 2-thiohydantoin, 4-thiohyantoin, 2-pyrazolin-5-one, 2-isoxazolin-5-one, indan-1,3-dione, cyclohexan-1,3-dione, 1,3-dioxan-4,6-dione, pyrazolin-3,5-dione, pentan-2,4-dione, alkylsulfonyl acetonitrile, malo-nonitrile, isoquinolin-4-one, and chroman-2,4-dione.

One or more spectral sensitizing dyes may be used. Dyes with sensitizing maxima at wavelengths through-out the visible spectrum and with a great variety of spec-tral sensitivity curve shapes are known. The choice and relative proportions of dyes depends upon the region of the spectrum to which sensitivity is desired and upon the shape of the spectral sensitivity curve desired. Dyes with overlapping spectral sensitivity curves will often yield in combination a curve in which the sensitivity at each wave-length in the area of overlap is approximately equal to thesum of the sensitivities of the individual dyes. Thus, it is possible to use combinations of dyes with different maxima to achieve a spectral sensitivity curve with a maximum intermediate to the sensitizing maxima of the individual dyes.
Combinations of spectral sensitizing dyes can be used which result in supersensitization--that is, spectral sensitization that is greater in some spectral region than that from any concentration of one of the dyes alone or that which would result from the additive effect of the dyes. Supersensitization can be achieved with selected combinations of spectral sensitizing dyes and other addenda, such as stabilizers and antifoggants, development acceler-ators or inhibitors, coating aids, brighteners and anti-static agents. Any one of several mechanisms as well ascompounds which can be responsible for supersensitization are discussed by Gilman, Photographic Science and Engineer-ng, Vol. 18, 1974, pp. 418-430.
Spectral sensiti~ing dyeQ also affect the emul-3 sions in other ways. For example, many spectral sensi-tizing dyes either reduce (desensitize) or increase photo-graphic speed within the spectral region of inherent sen-sitivity. Spectral sensitizing dyes can also funGtion as antifoggants or stabilizers, development accelerators or inhibitors, reducing or nucleating agents, and halogen acceptors or electron acceptors, as disclosed in Brooker et al U.S. Patent 2,131,038, Illingsworth et al U.S. Paten~
3,501,310, We~ster et al U.S. Patent 3,630,749, Spence et .,, :

- i: ~ " ~ i . -:

- ~ 5.~7~

al U.S. Patent 3,718,470 and Shiba et al U.S. Patent 3,930,860.
Sensitizing action can be correlated to the position o~ molecular energy levels of a dye with respect to ground state and conduction band energy levels of the silver halide crystals. These energy levels can in turn be corre-lated to polarographic oxidation and reduction potentials, as discussed in Photograæhic Science and Engineering, Vol.
18, 1974, pp. 49-53 (Sturmer et al), pp. 175-178 ~Leubner) and pp. 475-485 (Gilman~. Oxidation and reduction potentials can be measured as described by R. J. Cox, Photographic Sensitivity, Academic Press, 1973, Chapter 15.
The chemistry of cyanine and related dyes is illustrated by Weissberger and Taylor, Special Topics of Heterocyclic Chemistry~ John Wiley and Sons, New York, 1977, Chapter VIII; Venkataraman, The Chemistry of ~
thetic Dyes, Academic Press, New York, 1971, Chapter V;
James, The Theory o~ the Photographic Process, 4th Ed., Macmillan, 1977, Chapter 8, and F. M. Hamer, Cyanine Dyes and Related Compounds, John Wiley and Sons, 1964.
Among useful spectral sensitizing dyes for sensitizing silver halide emulsions are those found in U.K.
Patent 742,112, Brooker U.S. Patents 1,846,300, '301, '302, '303, '304, 2,078,233 and 2,089,729, Brooker et al U.S.
Patents 2,165,338, 2,213,238, 2,493,747, '748~ 2,526,632, 2,739,964 (Reissue 24,292), 2,778,823, 2,917,516, 3,352,857, 3,411,916 and 3,431,111, Sprague U.S. Patent 2,503,776, Nys et al U.S. Patent 3,282,933, Riester U.S. Patent 3,660,102, Kampfer et al U.S. Patent 3,660,103, Taber et al U.S.
3 Patents 3,335,010, 3,352,680 and 3,384,486, Lincoln et al U.S. Patent 3,397,981, Fumia et al U.S. Patents 3,482,978 and 3,623,881, Spence et al U.S. Patent 3,718,470 and Mee U.S. Patent 4,025,349. Examples of useful supersensitizing dye combinations, of non-light absorbing addenda which function as supersensitizers or of use~ul dye combinations are found in McFall et al U.S. Patent 2,933,390, Jones et al U.S. Patent 2,937,089, Motter U.S. Patent 3,506,443 and Schwan et al U.S. Patent 3,672,898.

.. . . . . .
.. . - . ~
.. ... ..

,:~ . .. , . . :
- .

'7~5 Instability which increases minimum density in negative type emulsion coatings ~i.e., fog~ can be protected against by incorporation o~ stabilizers, anti~oggants, antikinking agents, latent image stabilizers and similar addenda in the emulsion and contiguous layers prior to coating. Most of the antifoggants which are effective in emulsions can also be used in developers and can be classi-fied under a few general headings, as illustrated by C.E.K.
Mees, The Theory of the Photographic Process, 2nd Ed., Macmillan, 1954, pp. 677-680.
To avoid such instability in emulsion coatings stabilizers and antifoggants can be employed, such as halide ions (e.g., bromide salts~; chloropalladates and chloropalladites, as illustrated by Trivelli et al U.S.
Patent 2,566,263; water-soluble inorganic salts of cadmium, cobalt, manganese and zinc, as illustrated by Jones U.S.
Patent 2,839,405 and Sidebotham U.S. Patent 3,488,709;
mercury salts, as illustrated by Allen et al U.S. Patent 2,728,663; selenols and diselenides, as illustrated by Brown et al U.K. Patent 1,336,570 and Pollet et al U.K.
Patent 1,282,303; quaternary ammonium salts of the type illustrated by A~len et al U.S. Patent 2,694,716, Brooker et al U.S. Patent 2,131,038, Graham U.S. Patent 3,342,596 and Arai et al U.S. Patent 3,954,478; azomethine desensi-tizing dyes, as illustrated by Thiers et al U.S. Patent3,630,744; isothiourea derivatives, as illustrated by Herz et al U.S. Patent 3,220,839 and Knott et al U.S. Patent 2,514,650; thiazolidines, as illustrated by Scavron U.S.
Patent 3,565,625; peptide derivatives, as illustrated by 3 Maffet U.S. Patent 3,274,002; pyrimidines and 3-pyrazoli-dones, as illustrated by Welsh U.S. Patent 3,161,515 and Hood et al U.S. Patent 2,751,297; azotriazoles and azo-tetrazoles, as illustrated by Baldassarri et al U.S. Patent 3,925,086; azaindenes, particularly tetraazaindenes, as illustrated by Heimbach U.S. Patent 2,444,605, Knott U.S.
Patent 2,933,388, Williams U.S. Patent 3,202,512, Research Disclosure, Vol. 134, June 1975, Item 13452, and Vol. 148, ., . : . .: :

; ~ , . ,~ . ~ .. . . ..

7~5 August 1976, Item 14851, and Nepker et al U.K. Patent 1,338,567; mercaptotetrazoles, -triazoles and -diazoles, as illustrated by Kendall et al U.S. Patent 2,403,927, Kennard et al U.S. Patent 3,266,897, Research Disclosure, Vol. 116, December 1973, Item 11684, Luckey et al U.S. Patent 3,397,987 and Salesin U.S. Patent 3,708,303j azoles, as illustrated by Peterson et al U.S. Patent 2,271,229 and Research Disclosure, Item 11684, cited above; purines, as illustrated by Sheppard et al U.S. Patent 2,319,090, Birr et al U.S. Patent 2,152,460, Research Disclosure, Item 13452, cited above, and Dostes et al French Patent 2,296,204 and polymers of 1,3-dihydroxy(and/or 1,3-carba-moxy)-2-methylenepropane, as illustrated by Saleck et al U.S. Patent 3,926,635.
Among useful stabilizers for gold sensitized emulsions are water-insoluble gold compounds of benzo-thiazole, benzoxazole, naphthothiazole and certain mero-cyanine and cyanine dyes, as illustrated by Yutzy et al U.S. Patent 2,597,915, and sul~inamides, as illustrated by 20 Nishio et al U.S. Patent 3,498,792.
Among useful stabilizers in layers containing poly(alkylene oxides) are tetraazaindenes, particularly in combination with Group VIII noble metals or resorcinol derivatives, as illustrated by Carroll et al U.S. Patent 25 2,716,062, U.K. Patent 1,466,024 and Habu et al U.S. Patent 3,929,486; quaternary ammonium salts of the type illustrat-ed by Piper U.S. Patent 2,886,437; water-insoluble hydrox- :~
ides, as illustrated by Ma~fet U.S. Patent 2,953,455; ::
phenols, as illustrated by Smith U.S. Patents 2,955,037 and -3 '038; ethylene diurea, as illustrated by Dersch U.S. Patent 3,582,346; barbituric acid derivatives, as illustrated by Wood U.S. Patent 3,617,290; boranes, as illustrated by .
Bigelow U.S. Patent 3,725,078; 3-pyrazolidinones, as illus-trated by Wood U.K. Patent 1,158,059 and aldoximines, amidesj anilides and esters, as illustrated by Butler et al U.K. Patent 988,052. ~;

. . .

. . . . ..

The emulsion layers can be protected from fog and desensitization caused by contarnination by metals suc~ as copper, lead, tin, iron and the like, by incorporating addenda, such as sulfocatechol-type compounds, as illus-trated by Kennard et al U.S. Patent 3,236,652; aldoximines, as illustrated by Carroll et al U.K. Patent 623,448 and meta- and poly-phosphates, as illustrated by Draisbach U.S.
Patent 2,239,284, and carboxylic acids such as ethylene-diamine tetraacetic acid, as illustrated by U.K. Patent 10 691,715.
Among stabilizers use~ul in layers containing synthetic polymers of the type employed as vehicles and to improve covering power are monohydric and polyhydric phenols, as illustrated by Forsgard U.S. Patent 3,043,697;
15 saccharides, as illustrated by U.K. Patent 897,497 and Stevens et al U.K. Patent 1,039,471 and quinoline deriva-tives, as illustrated by Dersch et al U.S. Patent 3,446,618.
Among stabilizers useful in pro~cting the emul-sion layers against dichroic fog are addenda, such as salts 20 of nitron, as illustrated by Barbier et al U.S. Patents 3,679,424 and 3,820,998; mercaptocarboxylic acids, as illustrated by Willems et al U.S. Patent 3,600,178, and addenda listed by E. J. Birr, Stabilization of Photographic Silver Halide mulsions, Focal Press, London, 1974, pp.
25 126-218.
Among stabilizers useful in protecting emulsion layers against development fog are addenda such as azabenz-imidazoles, as illustrated by Bloom et al U.K. Patent 1,356,142 and U.S. Patent 3,575,699, Rogers U.S. Patent 30 3,473,924 and Carlson et al U.S. Patent 3,649,267; substi-tuted benzimidazoles, benzothiazoles, benzotriazoles andthe like, as illustrated by Brooker et al U.S. Patent 2,131,o38, Land U.S. Patent 2,704,721, Rogers et al U.S.
Patent 3,265,498 ; mercapto-substituted compounds, e.g., mercaptotetrazoles, as illustrated by Dimsdale et al U.S.
Patent 2,432,864, Rauch et al U.S. Patent 3,081,170, Weyerts et al U.S. Patent 3~260,597, Grasshoff et al U.S. Patent ;.'~

;. : . :.
., i , " . ~ : ",., "
' ~

- ~z~

3,674,478 and Arond U.S. Patent 3,706,557; isothiourea derivatives, as illustrated by Herz et al U.S. Patent 3,220,839, and thiodiazole derivatives, as illustrated by von Konig U.S. Patent 3,364,028 and von Konig et al U.K.
Patent 1,186,441.
Where hardeners of the aldehyde type are em-ployed, the emulsion layers can be protected with anti-foggants, such as monohydric and polyhydric phenols of the type illustrated by Sheppard et al U.S. Patent 2,165,421;
nitro-substituted compounds of the type disclosed by Rees et al U.K. Patent 1,269,268; poly(alkylene oxides), as illustrated by Valbusa U.K. Patent 1,151,914, and muco-halogenic acids in combination with urazoles, as illus-trated by Allen et al U.S. Patents 3,232,761 and 3,232,764, or further in combination with maleic acid hydrazide, as illustrated by Rees et al U.S. Patent 3,295,980.
To protect emulsion layers coated on linear polyester supports addenda can be employed such as para-banic acid, hydantoin acid hydrazides and urazoles, as 20 illustrated by Anderson et al U.S. Patent 3,287,135, and piazines containing two symmetrically fused 6-member car-bocyclic rings, especially in combination with an aldehyde-type hardening agent, as illustrated in Rees et al U.S.
Patent 3,396,023.
. Kink desensitization of the emulsions can be reduced by the incorporation of compounds, polymeric latices and dispersions of the type disclosed by Jones et al U.S.
Patents 2,759,821 and '822; azole and mercaptotetrazole hydrophilic colloid dispersions of the type disclosed by 3 Research Disclosure, Vol. 116, December 1973, Item 11684; ~;
plasticized gelatin compositions of the type disclosed by Milton et al U.S. Patent 3,033,680; water-soluble inter-polymers of the type disclosed by Rees et al U.S. Patent 3,536,491; polymeric latices prepared by emulsion polymeri-zation in the presence of poly~alkylene oxide~, as disclosed by Pearson et a:L U.S. Patent 3,772,032, and gelatin graft copolymers of the type disclosed by Rakoczy U.S. Patent 3,837,861.

~ . .

. . : . :, ., ~ . : :

fi 2~)'765 Where the photographic element is.to be processed at elevated ba~h or drying temperatures, as in rapid access processors, pressure desensitization and/or increased fog can be controlled by selected combinations of addenda, vehicles, hardeners and/or processing conditions, as illus-trated by Abbott et al U.S. Patent 3,295,976, Barnes et al U.S. Patent 3,545,971, Salesin U.S. Patent 3,708,303, Yamamoto et al U.S. Patent 3,615,619, Brown et al U.S.
Patent 3,623,873, Taber U.S. Patent 3,671~258, Abele U.S.
Patent 3,791,830, Research Disclosure, Vol. 99, July 1972, Item 9930, Florens et al U.S. Patent 3,843,364, Priem et al U.S. Patent 3,867,152, Adachi et al U.S. Patent 3,967,965 and Mikawa et al U.S. Patents 3,947,274 and 3,954,474.
In addition to increasing the pH or decreasing the pAg of an emulsion and adding gelatin, which are known to retard latent image fading, latent image stabilizers can be incorporated, such as amino acids, as illustrated by Ezekiel U.K. Patents 1,335,923, 1,378,354, 1,387,654 and 1,391,672, Ezekiel et al U.K. Patent 1,394,371, Jef~erson U.S. Patent 3,843,372, Je~ferson et al U.K. Patent 1,412,294 and Thurston U.K. Patent 1,343,904; carbonyl-bisulfite ~
addition products in combination with hydroxybenzene or ~-aromatic amine developing agents, as illustrated by Seiter ~
et al U.S. Patent 3,424,583; cycloalkyl-1,3-diones, as `.
illustrated by Beckett et al U.S. Patent 3,447,926; enzymes of the catalase type, as illustrated by Matejec et al U.S.
Patent 3,600,182; halogen-substituted hardeners in combina- ~
tion with certain cyanine dyes, as illustrated by Kumai et ..
al U.S. Patent 3,881,933; hydrazides, as illustrated by 3 Honig et al U.S. Patent 3,386,831; alkenylbenzothiazolium salts, as illustrated by Arai et al U.S. Patent 3,954,478;
hydroxy-substituted benzylidene derivatives, as illustrated by Thurston U.K. Patent 1,308,777 and Ezekiel et al U.K.
Patents 1,347,544 and 1,353,527; mercapto-substituted com-pounds of the type disclosed by Sutherns U.S. Patent 3,519,427;metal-organic complexes of the type.disclosed by Matejec et al U.S. Patent 3,639,128; penicillin derivatives, as illus-trated by Ezekiel U.K. Patent 1,389,089; propynylthio ~.

: ~ ~ . "

~. :: . , : ~ , .

derivatives of benzimidazoles, pyrimidines, etc., as illus-trated by von Konig et al U.S. Patent 3,910,791; combina-tions of iridium and rhodium compounds, as disclosed by Yamasue et al U.S. Patent 3,901,713; sydnones or sydnone imines, as illustrated by Noda et; al U.S. Patent 3,881,939;
thiazolidine derivatives, as illustrated by Ezekiel U.K.
Patent 1,458,197 and thioether-substituted imidazoles, as illustrated by Research Disclosure, ~ol. 136, August 1975, Item 13651.
The photographic elements can be color photo-graphic elements which form dye images through the selec-tive destruction, formation or physical removal of dyes.
The photographic elements can produce dye images through the selective destruction of dyes or dye precur-15 sors, such as silver-dye-bleach processes, as illustrated by A. Meyer, The Journal of Photographic Science, Vol. 13, 1965, pp. 90-97. Bleachable azo, azoxy, xanthene, azine, phenylmethane, nitroso complex, indigo, quinone, nitro-substituted, phthalocyanine and formazan dyes, as illus-20 trated by Stauner et al U.S. Patent 3,754,923, Piller et al U.S. Patent 3,749,576, Yoshida et al U.S. Patent 3,738,839, i~
Froelich et al U.S. Patent 3,716,368, Piller U.S. Patent 3,655,388, Williams et al U.S. Patent 3,642,482, Gilman U.S. Patent 3,567,448, Loeffel U.S. Patent 3,443,953, 25 Anderau U.S. Patents 3,443,952 and 3,211,556, Mory et al U.S. Patents 3,202,511 and 3,178,291 and Anderau et al U.S.
Patents 3,178,285 and 3,178,290, as well as their hydrazo, diazonium and tetrazolium precursors and leuco and shifted derivatives, as illustrated by U.K. Patents 923,265, 3 999,996 and 1,042,300, Pelz et al U.S. Patent 3,684,513, Watanabe et al U.S. Patent 3,615,493, Wilson et al U.S.
Patent 3,503,741, Boes et al U.S. Patent 3,340,059, Gompf et al U.S. Patent 3,493,372 and Puschel et al U.S. Patent 3,561,970, can be employed.
The photographic elements can produce dye images through the selective ~ormation o~ dyes, such as by react-ing ~coupling~ a color-developing agent ~e.g., a primary '' ; ' aromatic amine~ in its oxidized form with a dye-~orming coupler. The dye-forming couplers can be incorporated in the photographic elements, as illustrated by Schneider et al, Die Chemie, Vol. 57, 1944, p. 113, Mannes et al U.S.
Patent 2,304,940, Martinez U.S. Patent 2,269,158, Jelley et al U.S. Patent 2,322,027, Frolich et al U.S. Patent 2,376,679, Fierke et al U.S. Patent 2,801,171, Smith U.S.
Patent 3,748,141, Tong U.S. Patent 2,772,163, Thirtle et al U.S. Patent 2,835,579, Sa~dey et al U.S. Patent 2,533,514, 10 Peterson U.S. Patent 2,353,754, Seidel U.S. Patent 3,409,435 and Chen Research Disclosure, Vol. 159, July 1977, Item 15930.
In one form the dye-forming couplers are chosen to form subtractive primary ~i.e., yellow, magenta and cyan) image dyes and are nondiffusible, colorless couplers, such as two and four equivalent couplers of the open chain ketomethylene, pyrazolone, pyrazolotriazole, pyrazolobenz-imidazole, phenol and naphthol type hydrophobically bal-lasted for incorporation in high-boiling organic (coupler) solvents. Such couplers are illustrated by Salminen et al U.S. Patents 2,423,730, 2,772,162, 2,895,826, 2,710,803, 2,407,207, 3,737,316 and 2,367,531, Loria et al U.S.
Patents 2,772,161, 2,600,788, 3,006,759, 3,214,437 and 3,253,924, McCrossen et al U.S. Patent 2,875,057, Bush et al .U.S. Patent 2,908,573, Gledhill et al U.S. Patent 3,034,892, Weissberger et al U.S. Patents 2,474,293, 2,407,210, 3,062,653, 3,265,506 and 3,384,657, Porter et al U.S. Patent 2,343,703, Greenhalgh et al U.S. Patent 3,127,269, Feniak et al U.S. Patents 2,865,748, 2,933,391 and 2,865,751, Bailey et al U.S. Patent 3,725,067, Beavers et al U.S. Patent 3,758,308, Lau U.S. Patent 3,779,763, Fernandez U.S. Patent 3,785,829, U.K. Patent 969,921, U.K.
Patent 1,241,069, U.K. Patent 1,011,940, Vanden Eynde et al U.S. Patent 3,762,921, Beavers U.S. Patent 2,983,608, Loria U.S. Patents 3,311,476, 3,408,194, 3,458,315, 3,447,928, 3,476,563, Cressman et al U.S. Patent 3,419,390, Young U.S.
Patent 3,419,391, Lestina U.S. Patent 3,519,429, U.K.
Patent 975,928, U.K. Patent 1,111,554, Jaeken U.S. Patent : , . ~ . ~ j : .

7~
3,222,176 and Canadian Patent 726,651, Schulte et al U.K.
Patent 1,248,924 and Whitmore et al U.S. Patent 3,227,550.
The photographic elements can incorporate alkali-soluble ballasted couplers, as illustrated by Froelich et al and Tong, cited above. The photographic elements can be adapted to form non-diffusible image d~es using dye-forming couplers in developers, as illustrated by U.K. Patent 478,984~ Yager et al U.S. Patent 3,113,864, Vittum et al U.S. Patents 3,002,836, 2,271,238 and 2,362,598, Schwan et al U.S. Patent 2,950,970, Carroll et al U.S. Patent 2,592,243, Porter et al U.S. Patents 2,343,703, 2,376,380 and 2,369,489, Spath U.K. Patent 886,723 and U.S. Patent 2,899,306, Tuite U.S. Patent 3,152,896 and Mannes et al U.S. Patents 2,115,394, 2,252,718 and 2,108,602.
The dye-forming couplers upon coupling can release photographically useful fragments, such as devel-opment inhibitors or accelerators, bleach accelerators, developing agents, silver halide solvents, toners, hard-eners, fogging agents, antifoggants, competing couplers, chemical or spectral sensitizers and desensitizers.
Development inhibitor-releasing (DIR) couplers are illus-trated by Whitmore et al U.S. Patent 3,148,062, Barr et al U.S. Patent 3,227,554, Barr U.S. Patent 3,733,201, Sawdey U.S. Patent 3,617,291, Groet et al U.S. Patent 3,703,375, QbbQtt et al U.S. Patent 3,615,506, Weissberger et al U.S.
Patent 3,265,506, Seymour U.S. Patent 3,620,745, Marx et al U.S. Patent 3,632,345, Mader et al U.S. Patent 3,869,291, U.K. Patent 1,201,110, Oishi et al U.S. Patent 3,642,485, Verbrugghe U.K. Patent 1,236,767, Fu~iwhara et al U.S.
3 Patent 3,770,436 and Matsuo et al U.S. Patent 3,808,945.
DIR compounds which do not form dye upon reaction with oxidized color-developing agents can be employed, as illus-trated by Fujiwhara et al German OLS 2,529,350 and U.S.
Patents 3,928,041, 3,958,993 and 3,961,959, Odenwalder et al German OLS 2~448,063, Tanaka et al German OLS 2,610,546, Kikuchi et al U.S. Patent 4,049,455 and Credner et al U.S.
Patent 4,052,213. DIR compounds which oxidatively cleave can~be employed, as illustrated by Porter et al U.S. Patent 3,379,529, Green et al U.S. Patent 3,o43,690, Barr U.S.

.. . : :,, ~

.

37~;5 Patent 3,364,022, Duennebier et al U.S. Patent 3,2~7,4L15 and Rees et al U.S. Patent 3,287,129.
The photographic elements can incorporate colored dye-forming couplers, such as those employed to ~orm 5 integral masks for negative color images, as illustrated by Hanson U.S. Patent 2,449,966, Glass et al U.S. Patent 2,521,908, Gledhill et al U.S. Patent 3,034,892, Loria U.S.
Patent 3,476,563, Lestina U.S. Patent 3,519,429, Friedman U.S. Patent 2,543,691, Puschel et al U.S. Patent 3,028,238, Menzel et al U.S. Patent 3,061,432 and Greenhalgh U.K.
Patent 1,035,959, and/or competing couplers, as illustrated by Murin et al U.S. Patent 3,876,428, Sakamoto et al U.S.
Patent 3,580,722, Puschel U.S. Patent 2,998,314, Whitmore U.S. Patent 2,808,329, Salminen U.S. Patent 2,742,832 and 15 Weller et al U.S. Patent 2,689,793.
The photographic elements can produce dye images through the selective removal of dyes. Neg~tive or posi-tive dye images can be produced by the im~obilization or mobilization of incorporated color-providing substances 20 (e.g., redox dye-releasers) as a function of exposure and development, as illustrated by U.K. Patents 1,456,413, 1,479,739, 1,475,265 and 1,471,752, Friedman U.S. Patent 2,543,691, Whitmore U.S. Patent 3,227,552, Bloom et al U.S.
Patent 3,443,940, Morse U.S. Patent 3,549,364, Cook U.S.
25 Patent 3,620,730, Danhauser U.S. Patent 3,730,71~, Staples U.S. Patent 3,923,510, Oishi et al U.S. Patent 4,052,214 and Fleckenstein et al U.S. Patent 4,076,529.
The photographic elements can contain antistain agents (i.e., oxidized developing agent scavengers) to 30 prevent developing agents oxidized in one dye image layer unit from migrating to an adjacent dye image layer unit.
Such antistain agents include ballasted or otherwise non-diffusing antioxidants, as illustrated by Weissberger et al U.S. Patent 2,336,327, ~oria et al U.S. Patent 2,728,659, Vittum et al U.S. Patent 2,360,290, Jelley et al U.S.
Patent 2,403,721 and Thirtle et al U.S. Patent 2,701,197.
To avoid autooxidation the antistain agents can be employed in combination with other antioxidants, as illustrated by Knechel et al U.S. Patent 3,700,453.
::.
~ . , - . .
' . . ' , . ' .:` ~: ~ ', " :' . ~ :~ . ;:-. ;. :: i :`: - `'` ' :
... ... .
: . . .:: . . -~:~Z~

The photographic elements can include image dye stabilizers. Such image dye stabilizers are illustrated by U.K. Patent 1,326,889, Lestina et al U.S. Patents 3,432,300 and 3,698,909, Stern et al U.S. Patent 3,574,627, Brannock et al U.S. Patent 3,573,050, Arai et al U.S. Patent 3,764,337 and Smith et al U.S. Patent 4,042,394. 3 The sensitizing dyes and other addenda incor-porated into the layers of the photographic elements can be dissolved and added prior to coating either from ~ater or organic solvent solutions, depending upon the solubility of the addenda. Ultrasound can be employed to dissolve addenda, as illustrated by Owen et al U.S. Patent 3,485,634 and Salminen U.S. Patent 3,551,157. Semipermeable and ion exchange membranes can be used to introduce addenda, such as water soluble ions (e.g., chemical sensitizers).
Hydrophobic addenda, particularly those which need not be adsorbed to the silver halide grain surfaces to be effec-tive, such as couplers, redox dye-releasers and the like, can be mechanically dispersed directly, as illustrated by Belgian Patent 852,138, or in high boiling (coupler~ sol-vents, as illustrated by Jelley et al U.S. Patent 2,322,027 and ~ierke et al U.S. Patent-2,801,171, or the hydrophobic addenda can be loaded into latices and dispersed, as illus-trated by Chen Research Disclosure, Vol. 159, July 1977, Item 15930-Exemplary apparatus and procedures for intro-ducing and blending addenda are illustrated by Johnson et al U.S. Patents 3,425,835, 3,570,818, 3,773,302 and `
3,850,643, McCrossen et al U.S. Patent 3,342,605, Collins 3 et al U.S. Patent 2,912,343 and Terwilliger et al U.S.
Patents 3J827~888 and 3,888,465.
In forming photographic elements the layers can be applied to photographic supports by various procedures, including immersion or dip coating, roller coating, reverse roll coating, air knife coating, doctor blade coating, gravure coating, spray coating, extrusion coating, bead coating, stretch-flow coating and curtain coating. High speed coating using a pressure differential is illustrated by Beguin U.S. Patent 2,681,294. Controlled variation in ~ . .. . .
.
- , . : . : ,, .

.. ..
., . ~

., - . , : . .. ..

¢)765 the pressure differential to facilitate coating starts isillustrated by Johnson U.S. Patent 3,220,877 and to minimize splicing disruptions is illustrated by Fowble U.S. Patent 3,916,043. Coating at reduced pressures to accelerate drying is illustrated by Beck U.S. Patent 2,815,307. Very high speed curtain coating is illustrated l by Greiller U.S. Patent 3,632,374. Two or more layers can be coated simultaneously, as illustrated by Russell U.S.
Patent 2,761,791, Wynn U.S. Patent 2,941,898, Miller et al U.S. Patent 3,206,323, Bacon et al U.S. Patent 3,425,857, Hughes U.S. Patent 3,508,947, Herzhoff et al U.K. Patent 1,208,809, Herzhoff et al U.S. Patent 3,645,773 and Dittman et al U.S. Patent 4,001,024. In simultaneous multilayer coating varied coating hoppers can be used, as illustrated by Russell et al U.S. Patent 2,761,417, Russell U.S. Patents 2,761,418 and 3,474,758, Mercier et al U.S. Patent 2,761,419, Wright U.S. Patent 2,975,754, Padday U.S. Patent 3,oO5,Ll40, Mercier U.S. Patent 3,627,564, Timson U.S. Patents 3,749,053 and 3,958,532, Jackson U.S.
20 Patent 3,993~019 and Jackson et al U.S. Patent 3,996,885.
Silver halide layers can also be coated by vacuum evapora-tion, as illustrated by Lu Valle et al U.S. Patents 3,219,444 and 3,219,451.
The layers of the photographic elements can be coated on a variety of supports. Typical photographic supports include polymeric film, wood fiber--e.g., paper, metallic sheet and foil, glass and ceramic supporting elements provided with one or more subbing layers to en-hance the adhesive, antistatic, dimensional, abrasive, 3 hardness, frictional, antihalation and/or other properties of the support surface.
Typical of useful polymeric film supports are films of cellulose nitrate and cellulose esters such as cellulose triacetate and diacetate, polystyrene, poly-amides, homo- and co-polymers of vinyl chloride, poly(vinyl acetal~, polycarbonate, homo- and co-polymers of olefins, such as polyethylene and polypropylene, and polyesters of dibasic aromatic carboxylic acids with divalent alcohols, such as poly~ethylene terephthalate~.

- . ,,., . ~ -. ~ : ., . . ..
. ;~:: . : .
- : . ~.. . - . :

~7 6 Typical of useful paper supports are those which are partially acetylated or coated with baryta and/or a polyolefin, particularly a polymer of an ~-olefin contain-ing 2 to 10 carbon atoms, such as polyethylene, polypropyl- :.
ene, copolymers of ethylene and propylene and the like.
Polyolefins, such as polyethylene, polypropylene and polyallomers--e.g., copolymers of ethylene with propyl-ene, as illustrated by Hagemeyer et al U.S. Patent 3,478,128, are preferably employed as resin coatings over paper, as illustrated by Crawford et al U.S. Patent 3,411,908 and Joseph et al U.S. Patent 3,630,740, over polystyrene and polyester film supports, as illustrated by Crawford et al U.S. Patent 3,630,742, or can be employed as unitary flexible reflection supports, as illustrated by Venor et al U.S. Patent 3,973,963.
Preferred cellulose ester supports are cellulose triacetate supports, as illustrated by Fordyce et al U.S.
Patents 2,492,977, '978 and 2,739,069, as well as mixed cellulose ester supports, such as cellulose acetate 20 propionate and cellulose acetate butyrate, as illustrated by Fordyce et al U.S. Patent 2,739,070.
Preferred polyester film supports are comprised of linear polyester, such as illustrated by Alles et al U.S. Patent 2,627,088, Wellman U.S. Patent 2,720,503, Alles 25 u.s. Patent 2,779,684 and Kibler et al U.S. Patent -:
2,901,466. Polyester films can be formed by varied tech-niques, as illustrated by Alles, cited above, Czerkas et al `
U.S. Patent 3,663,683 and Williams et al U.S. Patent 3,504,075, and modified for use as photographic film 3 supports, as illustrated by Van Stappen U.S. Patent ~.
3,227,576, Nadeau et al U.S. Patent 3,501,301, Reedy et al U.S. Patent 3,589,905, Babbitt et al U.S. Patent 3,850,640, Bailey et al U.S. Patent 3,888,678, Hunter U.S. Patent 3,904,420 and Mallinson et al U.S. Patent 3,928,697.
The photographic elements can employ supports hich are resistant to dimensional.change at elevated temperatures. Such supports can be comprised of linear condensation polymers which have glass transition tempera-tures above about 190C, preferably 220C, such as poly-., ,,,; - ,, . , , .
., ~ . . .- ,. :: ::

13L;~(1~7~S

carbonates, polycarboxylic esters, polyamides, polysulfon-amides, polyethers, polyimides, polysulfonates and copoly-mer varian~s, as illustrated by Hamb U.S. Patents 3,634,089 and 3,772,405; Hamb et al U.S. Patents 3,725,070 and 3,793,249; Wilson Research Disclosure, Vol. 118, February 1974, Item 11833, and Vol. 120, April 1974, Item 12046; t Conklin et al Research Disclosure~ Vol. 120, April 1974, Item 12012; Product Licensing Index, Vol. 92, December 1971, Items 9205 and 9207; Research Disclosure, Vol. 101, September 1972, Items 10119 and 10148; Research Disclosure, Vol. 106, February 1973, Item 10613; Research Disclosure, Vol. 117, January 1974, Item 11709, and Research Disclosure, Vol. 134, June 1975, Item 13455.
The photographic elements of this invention show particularly advantageous sensitivities when exposed to light. The photographic elements are specifically contem-plated for imagewise exposure under ordinary lighting conditions--that is, less than high intensity lighting conditions. Exposures can be monochromatic, orthochro-matic or panchromatic. Imagewise exposures at ambient,elevated or reduced temperatures and/or pressures, con-tinuous or intermettent exposures 3 exposure times ranging from minutes to relatively short durations in the milli-second to microsecond range and solarizing exposures, can be employed within the useful response ranges determined by conventional sensitometric techniques, as illustrated by T. H. James, The Theory o~ the Photographic Process, 4th Ed., Macmillan, 1977, Chapters 4, 6, 17, 18 and 23.
Upon imagewise exposure the high chloride silver 3 halide grains form latent image sites at or near their sur-face, both in their primitive state and after surface chemi-cal sensitization, unless the emulsions as described above are otherwise modified. Accordingly the emulsions can be processed in all conventional silver halide developers--including those containing sufficient silver halide solventto reveal internal latent image sites, referred to in the art as surface and sub-surface developers, and those contain-ing higher levels of silver halide solvents, referred to in . . ~ .. :,, . .,.: : ~ . :

the art as internal developers. It is accordingly apparent that the emulsions as described above are useful for photo-graphic applications requiring negative-working silver halide emulsions and photographic elements.
The light-sensitive silver halide contained in the photographic elements can be processed ~ollowing exposure to form a visible image by associating the silver halide with an aqueous alkaline medium in the presence Or a developing agent contained in the medium or the element. Processing formulations and techniques are described in L. F. Mason, Photographic Processing Chemistry, Focal Press, London, 1966; ProcessingChemicals and Formulas, Publication J-l, ~astman Kodak Company, 1973; Photo-Lab Index, Morgan and Morgan, Inc., Dobbs Ferryg New York, 1977, and Neblette's Handbook of Photography and Reprography - Materials, Processes and Systems, VanNostrand Reinhold Company, 7th Ed., 1977.
Included among the processing methods are web processing, as illustrated by Tregillus et al U.S. Patent 3,179,517; stabilization processing, as illustrated by Herz et al U.S. Patent 3,220,839, Cole U.S. Patent 3,615,511, Shipton et al U.K. Patent 1,258,906 and Haist et al U.S.
Patent 3,647~453; monobath processing as described in Haist, Monobath ManuaI, Morgan and Morgan, Inc., 1966, Schuler U.S.
Patent 3,240,603, Haist et al U.S. Patents 3,615,513 and 3,628,955 and Price U.S. Patent 3,723,126; inf'ectious development, as illustrated b'y Milton U.S. Patents 3,294,537, 3,600,174, 3,615,519 and 3,615,524, Whiteley U.S. Patent 3,516,830, Drago U.S. Patent 3,615,488, Salesin et al U.S.
Patent 3,625,689, Illingsworth U.S. Patent 3,632,340, 3 Salesin U.K. Patent 1,273,030 and U.S. Patent 3,708,303;
hardening development, as illustrated by Allen et al U.S.
Patent 3,232,761; roller transport processing, as illustrated by Russell et al U.S. Patents 3,025,779 and 3,515,556, Masseth U.S. Patent 3,573,914, Taber et al U.S. Patent 3,647,459 and Rees et al U.K. Patent 1,269,268; alkaline vapor processing, as illustrated by Product Licensing Index, Vol. 97, May 1972, Item 9711, Goffe et al U.S. Patent 3,816,136 and King U.S. Patent 3,985,564; metal ion develop- ' ment as illustrated by Price, Photogr'aphic Science and . .

~2~7~

En~ineering, Vol. 19, Number 5, 1975, pp. 283-287 and Vought Research Disclosure, Vol. 150, October 1976, Item 15034;
reversal processing, as illustrated by Henn et al U.S.
Patent 3,5763633; and surface application processing, as illustrated by Kitze U.S. Patent 3,418,132.
The photographic elements can be processed to form dye images which correspond to or are reversals of the silver halide rendered selectively developable by imagewise exposure.
Multicolor reversal dye images can be formed in photographic elements having differentially spectrally sensitized silver halide layers by black-and-white devel-opment followed by i) where the elements lack inco~porated dye image formers, sequential reversal color development 15 with developers containing dye image formers, such as color couplers, as illustrated by Mannes et al U.S. Patent 2,252,718, Schwan et al U.S. Patent 2,950,970 and Pilato U.S. Patent 3,547,650; ii ) where the elem~ ts contain incorporated dye image formers, such as color couplers, a 20 single color development step, as illustrated by the Kodak Ektachrome E4 and E6 and Agfa processes described in British Journal of Photograph~ Annual, 1977, pp. 194-197, and British Journal of Photography, August 2, 1974, pp. 668-669; and iii) where the photographic elements contain bleach-25 able dyes, silver-dye-bleach processing, as illus-trated by the Cibachrome P-10 and P-18 processes described in the British Journal of Photogra~hy Annual, 1977, pp. 209-212. .
The photographic elements can be adapted for direct color reversal processing (i.e., production of 30 re~ersal color images without prior black-and-white devel-- opment), as illustrated by U.K. Patent 1,075,385, Barr U.S.
Patent 3,243,294, Hendess et al U.S. Patent 3,647,452, Puschel et al German Patent 1,257,570 and U.S. Patents 3,457,077 and 3,467,520, Accary-Venet et al U.K. Patent 35 1,132,736, Schranz et al German Patent 1,259,700, Marx et al German Patent 1,259,701 and Muller-Bore German OLS
2,005,091.

~ -2~q6 Multicolor dye images which correspond to the silver halide rendered selectively developable by imagewise exposure, typically negative dye images, can be produced by processing, as illustrated by the Kodacolor C-22, the Kodak Flexicolor C-41 and the Agfacolor processes described in British Journal of Photography Annual, 1977, pp. 201-205.
The photographic elements can also be processed by the Kodak Ektaprint-3 and -300 processes as described in Kodak Color Dataguide, 5th Ed., 1975, pp. 18-19, and the Agfa 10 color process as described in British Journal of Photog- )~
raphy Annual~ 1977, pp. 205-206, such processes being particularly suited to processing color print materials, such as resin-coated photographic papers, to form positive dye images.
The photographic elements can be processed in the presence of reducible species, such as transition metal ion complexes (e.g. cobalt(III) and ruthenium~III) complexes containing amine and/or ammine ligands~ and peroxy com-pounds (e.g. hydrogen peroxide and alkali metal perborates and percarbonates)-Dye images can be formed or amplified by pro-cesses which employ in combination with a dye-image-generat-ing reducing agent an inert transition metal ion complex oxidizing agent, as illustrated by Bissonette U.S. Patents 25 3,748,138, 3,826,652, 3,862,842 and 3,989,526 and Travis U.S. Patent 3,765,891, and/or a peroxide oxidizing agent, as illustrated by Matejec U.S. Patent 3,674,490, Research Disclosure, Vol. 116, December 1973, Item 11660, and Bissonette Research Disclosure, Vol. 148, August 1976, 3 Items 14836, 14846 and 14847. The photographic elements can be particularly adapted to form dye images by such processes, as illustrated by Dunn et al U.S. Patent 3,822,129, Bissonette U.S. Patents 3,834,907 and 3,202,905, Bissonette et al U.S. Patent 3,847,612 and Mowrey U.S. Patent 3,904,413.
The presence of transition metal ion complexes can accelerate silver halide development, as illustrated by Bissonette U.S. Patent 3,748,138, Beavers U.S. Patent 3,901,712 and Price U.S. Patent 3,964,212; can bleach silver . .. :

.

images, as illustrated by Bissonette U.S. Patent 3,923,511 and Research Disclosure, Item 14846, and can be employed to ~orm tanned colloid images, as illustrated b~ Bissonette U.S. Patent 3,856,524 and McGuckin U.S. Patent 3,862,855.
The peroxide oxidizing agents can be employed to form vesicular images, as illustrated by ~eyde U.S. Patent 3,615,491, Weyde et al U.K. Patent 1,329,444 and U.S. Patent 3,765,890, Meyer et al U.K. Patent 1,332,693, Liebe et al German OLS 2,420,521 and Mate~ec et al U.S. Patent 3,776,730.
The emulsions and photographic elements of this invention can rorm a part o~ an otherwise conventional image transfer system. Image transfer systems include colloid transfer systems~ as illustrated by Yutzy et al U.S. Patents 2,596,756 and 2,716,059; silver salt diffusion 15 transfer systems, as illustrated by Rott U.S. Patent ~:
2,352,014, Land U.S. Patent 2,543,181, Yackel et al U.S.
Patent 3,020,155 and Land U.S. Patent 2,861,885; imbibition transfer systems, as illustrated by Minsk U.S. Patent 2,882,156, and color image trans~er systems, as illustrated ~
by Research Disclosure, Vol. 151, November 1976, Item .
15162, and Vol. 123, July 1974, Item 12331.
Color image transfer systems (including emulsion layers, receiving layers, timing layers, acid layers, pro-cessing compositions, supports and cover sheets) and the .~-25 images they produce can be varied by choosing among a ~.
variety of features, combinations of which can be used together as desired.
Film units can be chosen which are either inte-grally laminated or separated during exposure, processing 3 and/or viewing, as illustrated by Rogers U.S. Patent 2,983,606, Beavers et al U.S. Patent 3,445,228, Whitmore Canadian Patent 674,082, Friedman et al U.S. Patent 3,309,201, Land U.S. Patents 2,543,181, 3,053,659, 3,415,644, 3,415,645 and 3,415,646 and Barr et al U.
Patent 1,330,524. ~
Positive-wor~ing chemistry can be chosen utiliz- `
ing initially mobile dyes which are immobilized by develop- ;
ment, as illustrated by Rogers U.3. Patent 2,983,606, Yutzy U.S. Patent 2,756,142, Lestina et al U.S. Patent 3,880,658, :~"

~21~7f~5 Bush et al U.S. Patent 3,854,945 and Janssens et al U.S.
Patent 3,839,c35, or initially immobile dyes which are rendered mobile by development, as illustrated by Hinshaw et al U.K. Patent 1, 464,104 and Fields U.S. Patent 3,980,479; or negative-working imaging chemistry can be chosen utilizing the release of diffusible dyes from an immobile image dye-forming compound (e.g., a redox dye-releaser) as a function of development, as illustrated by Belgian Patent 838,062, Whitmore et al Canadian Patent 602,607 and U.S. Patent 3,227,550, Bloom et al U.S. Patent 3,443,940, Puschel et al U.S. Patents 3,628,952 and 3,844,785, Gompf et al U.S. Patent 3,698,897, Anderson et al U.S. Patent 3,725,062, Becker et al U.S. Patent 3,728,113, Fleckenstein U.S. Patent 4,053,312, Fleckenstein et al U.S. Patent 4,076,529, r~elzer et al U.K. Patent 1,489,695, Degauchi German OLS 2,729,820 and Kestner et al Research Disclosure, Vol. 151, November 1976, Item 15157.
An image to be viewed can be transferred from the image-forming layers. A retained image can be formed for 20 viewing as a concurrently formed complement of the trans-ferred image. Positive transferred images and useful negative retained images can be formed when one of the imaging chemistry and the emulsion is negative-working and the other positive-working; and negative transferred images 25 and positive retained images can be formed when both the imaging chemistry and the emulsion(s) are negative-working or positive-working. Images retained in and transferred from the image-forming layers are illustrated by U.K.
Patent 1,456,413, Friedman U.S. Patent 2,543,691, Bloom et 3 al U.S. Patent 3,443,940, Staples U.S. Patent 3,923,510 and Fleckenstein et al U.S. Patent 4,076,529.
One-step processing can be employed, as illus-trated by U.K. Patent 1,471,752, Land U.S. Patent 2,543,181, Rogers U.S. Patent 2,983,606 ~pod processing~, Land U.S.
Patent 3,485,628 ~soak image-former and laminate to receiv-er~ and Land U.S. Patent 3,907,563 ~soak receiver and laminate to image-forming element~; or multi-step process-ing can be employed, as illustrated by ~ut~y U.S. P~ltent ' ~

~2~ S

2,756,142, Whitmore et al U.S. Patent 3,227,550 and Faul et al U.S. Patent 3,998,637.
Pre~ormed reflective layers can be employed as illustrated by Whitmore Canadian Patent 674,082, Beavers u.s. Patent 3,445,228, Land U.S. Patents 2,5L~3,181, 3,415,644, 3~415,645 and 3,415,646, and Barr et al U.K.
Patent 1,330,524; or processing-f`ormed reflective layers can be employed, as illustrated by Land U.S. Patents 2,607,685 and 3,647,437, Rogers U.S. Patent 2,~83,606 and Buckler U.S. Patent 3,661,585.
In addition to the silver halide emulsion and photographic element features specifically indicated above, it is appreciated that other conventional features requir-ing no detailed description can also be present. For 15 example, the photographic elements can contain brighteners, absorbing and scattering materials, hardeners, coating aids, plasticizers and lubricants, antistatic layers, matting a~ents, developing agents and development modi~iers as des-cribed in Paragraphs V, VIII, X, XI, XII, XIII, XVI, XX and XXI, of Research Disclosure, Vol. 176, December 1978, Item 17643. Still other conventional photographic features and applications not inconsistent with this invention will be readily apparent to those skilled in the art.
Product Licensing Index and Research Disclosure 25 are published by Industrial Opportunities Ltd., Homewell, Havant, Hampshire, PO9 lEF, United Kingdom.
In a specific preferred form the photographic elements of this invention are intended to produce multi-color images which can be viewed in the elements or in a 3 receiver when the elements form a part of a multicolor image transfer system. For multicolor imaging at least three superimposed color-forming layer units are coated on a support. Each of the layer units is comprised of at - least one silver halide emulsion layer. At least one of 35 the silver halide emulsion layers, preferably at least ;~
one of the silver halide emulsion layers in each color forming layer unit and most preferably each of the silver halide emulsion layers, contain an emulsion according to this invention substantially as described above. The .. ...

emulsion layers of one of the layer units are primarily responsive to the blue region of the spectrum, the emulsion layers of a second of the layer units are primarily respon-sive to the green region of the spectrum, and the emulsion layers of a third of the layer units are primarily respon-sive to the red region of the spectrum. Since the high chloride silver halide emulsions exhibit only limited native sensitivity to the visible portion of the spectrum, the use of yellow filter dyes between ad;acent layer units can be omitted in many instances and the layer units can be coated in any desired order. The layer units each contain in the emulsion layers or in adJacent hydrophilic colloid layers at least one image dye providing compound. Such compounds can be selected from among those described above.
Incorporated dye-forming couplers and redox dye-releasers constitute exemplary preferred image dye providing means.
The blue, green and red responsive layer units preferably contain yellow, magenta and red image dye providing means, respectively.

'.: ', ~ ~' - '' .:
- . , . :-... . ..

. .: : . ~.. ~ " ' :: - :

- : :, ::

~2~765 The invention is further illustrated by the following examples.
Example 1 lA. A polydisperse silver chloride emulsion, mean grain size about 0.45 ~m, was prepared in the following manner:
Two solutions were prepared as ~ollows:
Solution 1 (Placed in the Reaction Vessel) Gelatin 100 g 10 Distilled Water 7000 ml Sodium Chloride 425 g Dissolve at 40C
Adjust pH to 3.0 with HN03 Solution 2 15 Silver Nitrate 850 g Distilled Water to 2900 ml total volume Dissolve at 40C
Adjust pH to 3.0 with HNO3 To solution 1 were added 1.7 mg of a fog inhibiting agent of the type described in Allen et al U.S. Patent 2,728,663. Solution 2 was then added to the reaction vessel, at a constant flow rate, over a 40 minute period, with con-tinuous agitation. Following precipitation the pH was adjusted to 4.5, a pH coaguable gelatin derivative was added to the emulsion, and the emulsion was washed using the pro-cedure described in Example 3 of Yutzy et al U.S. Patent 2,614,929.
lB. A cadmium doped polydisperse silver chloride emul-3 sion, mean grain size about 0.45 ~m, was prepared as described above, except that 10 mg o~ cadmium chloride (1.1 x 10 5 mole/
Ag mole) were added to the reaction vessel 5 minutes after the start of the precipitation.
The polydisperse silver chloride emulsions prepared as described above were coated, unsensitized and optimally gold sensitized~ on a cellulose acetate film support at cover-ages of 6.90 g gelatin and 4.65 g Ag/m2. The coated elements were then exposed through a graduated density step wedge, developed for 5' in Kodak Developer DK-50, fixed, washed and dried. The sensitometric results are set forth below in Table II.
TABLE II
Cadmium Gold Relative 5 Internal DopantSensitized Speed No No lO0 Yes No 132 No Yes 355 Yes yes 501 lO From Table II it can be seen that the inclusion o~ j cadmium as a dopant in a polydisperse silver chloride emulsion unexpectedly results in an increase in speed of the emulsion compared to an emulsion similarly prepared but lacking a cadmium dopant.
Example 2 2A. A monodisperse silver chloride emulsion (1.5 ~m) was prepared in the following manner:
Three solutions were prepared as ~ollows:
Solution l (Placed in the Reaction Vessel) Gelatin lO0 g Distilled Water 7000 ml Dissolve at 40C
Ad~ust pH to 2.0 Solution 2 -Sodium Chloride 425 g Distilled Water to 2900 ml total volume Dlssolve at 40C
Solution 3 Silver Nitrate 850 g Distilled Water to 2900 ml total volume Dissolve at 40C
To so:Lution l were added 2.5 g of a silver halide ripening agent of the type describe~ in McBride U.S. Patent 3,271,157. The pAg o~.solution l was then adJusted to 8.0 using solution 2. Solutions 2 and 3 were then simultaneously . - .:

,: . , : :, -- . : . .
:, ~2~7 6 run into solution 1 over a 40 minute period using an accelerated flow technique, maintaining the pAg at 8.o.
Following precipitation the pH was raised to 5.5, a pH
coaguable gelatin derivative was added to the emulsion, and the emulsion was washed using the procedure described in Example 3 of Yutzy et al U.S. Patent 2,614,929.
2B. A cadmium doped monodisperse silver chloride - emulsion (1.5 ~m) was prepared as described above (A), except that 10 mg of cadmium chloride (1.1 x 10 5 mole~Ag mole) were added to the reaction vessel prior to the start of the precipitation.
The monodisperse silver chloride emulsions pre-pared as described above (A and B) were optimally gold sensitized and coated and tested as described in Example 1. The sensitometric results are set forth below in Table III.
TABLE III
Cadmium Relative Internal Dopant Speed No 100 Yes 162 From Table III it can be seen that the inclusion of cadmium as a dopant in a monodisperse silver chloride emulsion unexpectedly results in an increase in speed of the emulsion compared to an emulsion similarly prepared but lacking a cadmium dopant.
Example 3 A series of monodisperse silver chloride emul- ;
sions of approximately equal grain size (1.4-1.5 ~m) were 3 prepared by a method similar to that utilized in Example 2, except that varying amounts of cadmium c~hloride were added to the reaction vessel 5 minutes after the start of precipitation. The resulting emulsions were then opti-mally gold sensitized, coated and processed as described in Example 1. ~able I~ shows the concentrations of cadmium chloride utillzed in the various emulsions. Relative speeds for these emulsions are shown in Curve A in Figure 1.

~.
; .... , ~ 7 ~ 5 TABLE I~
Cadmium Chloride Emulsion mg/~ mole Mole~Ag mole ~rain Siæe (.~-m) No cadmium chloride added 1.5 5 o.5 2.75 X 10-6 1.4 1.0 5.5 X 10-6 1.5 2.0 1.1 X 10-5 1.5

4.0 2.2 X 10-5 1.5 8.o 4.4 x 10-5 1.5 1012.0 6.6 X 10-5 1.5 Example 4 A series of monodisperse silver chloride emulsions were prepared by a method similar to that described in Example 2, except that varying amounts of lead chloride were added 5 minutes after the start of the precipitation. The resulting emulsions were then optimally gold chemically sensitized and processed as described in Example 1. Table V
shows the concentrations of lead chloride ~tilized. Relative speeds are shown in Curve B in Figure 1. ~
20TABLE ~ :
Lead Chloride Emulsion ~:~ ~ V~ 6 r~ie Grain Size (~m) No lead chloride added 1.5 1.0 3.6 X 10-6 1.4~ ~
. 2,0 7.2 X 10-6 1.5 ' ~.
4.0 1.4 X 10-5 1.5 Example 5 A series of monodisperse silver chloride emulsions were prepared by a method similar to that described in 30 Example 2, except that the doped emulsions were prepared by ~-adding 10 mg of either copper chloride or ~inc chloride to the reaction vessel 5 minutes after the start of the precipi-tation. The resulting emulsions were then optimally gold chemically sensitized, coated and processed as described in Example 1. Table ~I below shows the concentration of the dopants utilized and the relative speeds are shown for the copper and Zinc doped emulsions at points C and D, respec- :
tively, in Figure 1.

TABLE ~I
Metal mg/AgMoles/Ag Emulsion Dopant Mole Mole Grain Si~e (~m) None --- --- 1. 5 CuC12 2.Q 1.5 X 10-5 1.6 ZnC12 2.01.47 x 10-5 1. 5 Example 6 A. A silver chlorobromide emulsion (:20 mole percent bromide) lacking an internal metal dopant was prepared in 10 the following manner: ) Three solutions were prepared as follows:
Solution 1 (Placed in the Reaction Vessel) Gelatin 100 g Distilled water 7000 ml Dissolve at 40C, Ad~ust pH to 2.0 Solution 2 Sodium chloride 367 g Potassium bromide 119 g Distilled water to total volume at 40C 2900 ml Solution 3 Silver nitrate 850 g Distilled water to total volume 2900 ml Dissolve at 40c To solution 1 were added 2.5 g of a silver halide ripening agent o~ the type disclosed in McBride U.S. Patent 3 3,271,157. The pAg of solution was then adjusted to 7.94 with solution 2. Solutions 2 and 3 were then simultaneous-ly run into solution 4 over a 40 minute period using an accelerated ~low technique, maintaining the pAg at 7.94.
Following precipitation a pH coagulable gelatin derivative 35 was added to the emulslon, and the emulsion was ~as~ed using the procedure described in Example 3 o~ Yutzy et al U.S. Patent 2,~14,92~.
B. A cadrnium doped silver chlorobromide emulsion (20 mole percent bromide~, was prepared as described in : .

- .: . . :, .: i . : , ~

. ..,~, . .' . ' ., ! , .. ~

_L,7_ paragraph A above except that 10 mg of cadmium chloride (1.1 X 10 5 mole/Ag mole) were added to the reaction vessel 5 minutes after the start of the precipitation.
C. A silver chlorobromide emulsion (50 mole percent bromide) was prepared as in Paragraph A, except that the amounts of sodium chloride and potassium bromide utilized in the preparation of solution 2 were 279 g and 2~8 g, respec-tively.
D. A cadmium doped silver chlorobromide emulsion (50 mole percent bromide) was prepared as described in Paragraph C, except that the lQ mg of cadmium chloride (1.1 X 10 5 mole/Ag mole) were added to the reaction vessel 5 minutes after the start of precipitation.
E. The silver chlorobromide emulsions prepared in Paragraphs A-D were optimally gold chemically sensitized, coated and processed as described in Example 1. Table VII
shows the fog levels.
TABLE VII
AgClBr Cadmium Dopant 20 (mole mg~Ag~ole/Ag Emulsion % Br) MoleMole _ Grain Size (~m) NoneNone 1.0 2.01.1 X 10-5 1.0 NoneNone 0.8 2.a1.1 X 10-5 o.8 --In Figure 2 a plot is provided of the increase in relative speed versus the halide content. The increase in relative -speed is obtained by taking the relative speed of a photo-graphic element formed with an undoped, surface chemically sensitized emulsion as 100 and plotting as an ordinate the additional speed of an otherwise identical element formed with an emulsion differing by containing a dopant, as described above. The abscissa is plotted in terms of mole percent, the mole percent chloride in the silver halide ;
emulsion being the numerator and the mole percent bromide in the silver halide emulsion being the denominator.
Example 7 A series of six monodisperse silver chloroiodide emulsions (0.7 ~m~, were prepared in a manner similar to '7 ~48-Example 2 except that a constant flow technique was ut:lized rather than an accelerated flow and the precipitation was carried out at a temperature of 6QC. The emulsion series contains two siiver chloroiodide emulsions (undoped and doped with 2 mg/Ag mole of cadmium chloride~ at each of three separate chloride/iodide ratios, lQ0~0, ~8~2 and 96/4.
The emulsions having these chloride/iodide ratios were pre-pared by adding either 0, 16.6 or 33.2 g of potassium iodide, respectively, to solution 2 prior to precipitation. The resulting emulsions were coated, exposed and processed by the method described in Example 1. In Figure 3 a plot is pro-vided of the increase in relative speed achieved by doping versus the halide ratio.
Example 8 Two incorporated coupler color print materials were prepared in the same manner, except differing in the emulsions utilized in the blue-sensitive, yellow dye-forming layer. The multilayer coatings were prepared in the following manner:
Separate portions of a polyethylene coated paper support were coated with gelatin layers comprising the yellow dye-forming coupler ~-[4-(4-benzyloxyphenylsulfonyl~
phenoxy]-~-pivalyl-2-chloro-5-[y-butyramido]-acetanilide at a coverage of 1.07 g/m and optimally gold chemically sensitized silver chloride emulsions prepared as described in Example 2 at a coverage of 0.33 g Ag/m2. The silver chloride emulsions were both spectrally sensitized to the blue region of the visible spectrum using a blue spectral sensitizer. The rest of the multilayer coating for each of the above variations are common and are described as a gelatin interlayer comprising gelatin and an antistain agent; a magenta dye-forming layer comprising a green-sensitized silver chloride emulsion, a magenta dye-forming coupler and gelatin; an interlayer comprising gelatin, an antistain agent and a UV absorber; a cyan dye-~orming layer comprising a red sensitized silver chloride emulsion, a cyan dye-forming coupler and gelatin and a protective overcoat layer comprising gelatin. The multilayer photosensitive ;
.

.. ..

' : ' '' ' ~

elements were then exposed to a tungsten light source through a graduated density step wedge and processed in a 3-solution color process of the type described in Edens et al U.S. Reissue Patent ~8,112. The relative blue sensi-tivities of the two processed materials are shown in TableVIII.
TABLE VIII
Emulsion in Blue- Cadmium Relative Sensitive, Yellow Chloride Blue Dye-Forming_Layer Dopant Sensitivity AgC1 None 100 AgCl2 mg/Ag Mole 182 Example 9 Two multicolor negative image-forming elements suitable for use in a color image transfer process, wherein color prints are obtained through the use of color nega-tives, were prepared. The elements were identical, except for the emulsions utilized in the blue sensitized, yellow dye-releasing unit. The elements were prepared as des-cribed below. The quantities of components are stated as grams/meter2 in parenthesis. Silver halide quantities are given in terms of silver.
A poly(ethylene terephthalate~ film support coated on one side with a carbon-pigmented gelatin layer was coated on the other side with the following layers:
(1) a cyan dye-providing layer comprising a disper-sion of a cyan redox dye-releaser and gelatin;
(2) a light-sensitive layer comprising a red sensi-tized, chemically sensitized silver chloride emulsion;
3 (3) interlayer comprsing gelatin and an antistain agent;
(4) a magenta dye-providing layer comprising a dispersion of a magenta redox dye-releaser and gelatin,

(5) a light-sensitive layer compring a green sensi-tized, chemically sensitized silver chloride ~-emulsion and gelatin; ~

.. .. -,. ...
: , - ,,., .. .: ~
. : : : : : -- . .: : . ::
,: :: :- :

(6) interlayer comprising gelatin and an antistain agent;

(7) a yellow dye-providing layer comprising a dis-persion of Compound A~ ~a yellow redox dye-releaser) (0.49) and gelatin Cl. 07);
Separate samples of ~he above-described element were then i , overcoated with layers comprising gelatin (1.07~ and chemically sensitized silver chloride (0.30) emulsions prepared either as described in Control 4 or as in Example 10 1. The silver chloride emulsions ~ere both spectrally sensitized to the blue region o~ the visible spectrum using a blue spectral sensitizer. Each sample was pro-vided with a gelatin overcoat layer.
*Compound A
OH

t ~ C O N ( C, 8 H 3 7 ) 2 NHSO~ HO
2 0 O~s ~ - N= N- o~ 1 6 6 = N
Cl CN

Samples of each element were identically exposed to blue ligh,t through a graduated density test ob~ect and pro-cessed as follows:
The exposed elements were soaked for 10 seconds at 28C in an activator solution comprising water to 1000 ml, benzyl alcohol (10 ml), 5-methylbenzotriazole (1 g), 3 ll-aminoundecanoic acid (2 g~ and 6-aminohexanoic acid, laminated to a receiving element Cdescribed below~ for 2 1/2 minutes at 24C, and then peeled apart. The trans-ferred yellow dye images produced in the receiving element ,, were evaluated and the results are shown below in Table ~"~
IX.

TABLE IX
Cadmium Relative Emulsion in Blue- Chloride Blue Sensitive Layer . Dopant Sensitivity AgCl None lO0 AgCl 2 m~/Ag Mole 162 Receiving Element The receiving element utilized comprised a paper support overcoated with a white-pigmented polyethylene layer, an acid layer comprising co-poly(styrene-maleic anhydride), a polymeric timing layer, a receiving layer comprising gelatin, 4-hydroxymethyl4-methyl-1-phenyl-3-pyrazolidone, poly(N-vinylimidazole-co-3-hydroxyethyl-l-vinylimidazolium chloride) (90:10 weight ratio) and a gelatin overcoat layer.
The invention has been described with particular reference to certain preferred embodiments thereof but it will be understood that variations and modi~ications can be effected within the spirit and scope of the invention.

- .

.~ . .

.:

Claims (32)

WHAT IS CLAIMED IS

1. A silver halide emulsion of the developing out type comprised of silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent silver iodide, based on total silver halide, said silver halide grains being internally doped with cadmium, lead, copper, zinc or mixtures thereof in a speed increas-ing amount of up to 7 X 10-5 mole per mole of silver halide.

2. A silver halide emulsion of the developing out type comprised of silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent silver iodide, based on total silver halide, said silver halide grains being formed in the presence of cadmium, lead, copper, zinc or mixtures thereof in a concentration of from 2 X 10-6 to 7 X 10-5 mole per mole of silver halide.

3. A silver halide emulsion according to claim 1 in which said silver halide grains consist essentially of silver chloride.

4. A silver halide emulsion according to claim 1, 2 or 3, in which said silver halide grains are formed in the presence of cadmium, zinc or mixtures thereof in a concentration of from 3 X 10-6 to 6 X 10-5 mole per mole of silver halide.

5. A silver halide emulsion according to claim 1, 2 or 3, in which said silver halide grains are formed in the presence of lead, copper or mixtures thereof in a concentration of from 3 X 10-6 to 5 X 10-5 mole per mole of silver halide.

6. A silver halide emulsion according to claim 1, 2 or 3, in which said silver halide grains are substan-tially monodispersed.

7. A silver halide emulsion according to claim 1, 2 or 3, in which said silver halide grains are gold sensitized.

8. A silver halide emulsion according to claim 1, 2 or 3, in which said silver halide grains are sulfur and gold sensitized.

9. In a photographic element of the developing out type comprised of a support and, coated on said support, a silver halide emulsion layer, the improvement comprising said silver halide emulsion layer being comprised of silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent silver iodide, based on total silver halide, said silver halide grains being internally doped with cadmium, lead, copper, zinc or mixtures thereof in a speed increasing amount of up to 7 X
10-5 mole per mole of silver halide.

10. In a photographic element of the developing out type comprised of a support and, coated on said support, a silver halide emulsion layer, the improvement comprising said silver halide emulsion layer being comprised of silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent silver iodide, based on total silver halide, said silver halide grains being formed in the presence of cadmium, lead, copper, zinc or mixtures thereof, in concentrations of from 2 X 10-6 to 7 X 10-5 mole per mole of silver halide.

11. In a photographic element of the developing out type comprised of a support and, coated on said support, a silver halide emulsion layer, the improvement comprising said silver halide emulsion layer being comprised of a gelatino-silver halide emulsion containing gold sensi-tized silver halide grains which consist essentially of at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, formed in the presence of cadmium in a concentration of from 2 X
10-6 to 7 X 10-5 mole per mole of silver halide.

12. In a photographic element of the developing out type comprised of a support and, coated on said support, a silver halide emulsion layer, the improvement comprising said silver halide emulsion layer being comprised of a gelatino-silver halide emulsion containing gold sensitized silver halide grains which consist essentially of at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, formed in the presence of zinc in a concentration of from 2 X 10-6 to 7 X 10-5 mole per mole of silver halide.

13. In a photographic element according to claim 11 or 12 the further improvement in which said silver halide grains are formed in the presence of from 5 X 10-6 to 2.5 X
10-5 mole zinc or cadmium per mole of silver halide.

14. In a photographic element of the developing out type comprised of a support and, coated on said support, a silver halide emulsion layer, the improvement comprising said silver halide emulsion layer being comprised of a gelatino-silver halide emulsion containing gold sensi-tized silver halide grains which consist essentially of at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, formed in the presence of lead in a concentration of from 2 X 10-6 to 7 X 10-5 mole per mole of silver halide.

15. In a photographic element of the developing out type comprised of a support and, coated on said support, a silver halide emulsion layer, the improvement comprising said silver halide emulsion layer being comprised of a gelatino-silver halide emulsion containing gold sensi-tized silver halide grains which consist essentially of at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, formed in the presence of copper in a concentration of from 2 X
10-6 to 7 X 10-5 mole per mole of silver halide.

16. In a photographic element according to claim 14 or 15 the further improvement in which said silver halide grains are formed in the presence of from 8 X 10-6 to 2 X
10-5 mole lead or copper per mole of silver halide.

17. In a photographic element according to claim 11 or 12 the further improvement in which said support is a transparent film support or a reflective paper support.

18. In a photographic element according to claim 14 or 15 the further improvement in which said support is a trans-parent film support or a reflective paper support.

19 . In a photographic element of the developing out type capable of producing multicolor dye images com-prised of a support and, coated on said support, at least three superimposed color-forming layer units, one of said layer units containing a blue responsive silver halide emulsion and a yellow image dye providing means, a second of said layer units containing a green responsive silver halide emulsion and a magenta image dye providing means and a third of said layer units containing a red responsive sil-ver halide emulsion and a cyan image dye providing means, the improvement comprising at least one of said silver halide emulsions being comprised of silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent iodide, based on total silver halide, said silver halide grains being formed in the presence of cadmium, lead, copper, zinc or mixtures thereof, in a concentration of from 2 X 10-6 to 7 X 10-5 mole per mole of silver halide.

20 . In a photographic element capable of forming a multicolor dye image according to claim 19 the further improvement in which the photographic element forms a part of a multicolor image transfer system.

21. In a photographic element capable of forming a multicolor dye image according to claim19 or 20 the further improvement in which said silver halide emulsions consist essentially of silver chloride.

22. In a process of forming a silver halide emulsion of the developing out type by reacting a water soluble silver salt with one or more water soluble halide salts in an aqueous medium containing a peptizer to form radiation-sensitive silver halide grains, the improvement comprising forming silver halide grains which are at least 80 mole percent silver chloride and less than 5 mole percent iodide, based on total silver halide, and introducing into the aqueous medium during formation of the silver halide grains cadmium, lead, copper, zinc or mixtures thereof, in a total concentration of from 2 X 10-6 to 7 X 10-5 mole per mole of silver halide.

23. In a process of forming a silver halide emulsion of the developing out type by a double-jet precipi-tation process in which an aqueous silver salt and at least one aqueous halide salt are separately and concurrently introduced into a reaction vessel in the presence of a gelatin or gelatin derived peptizer to form radiation-sensitive silver halide grains and surface chemically sensitizing the silver halide grains with a gold sensitizer, the improvement comprising forming silver halide grains which are at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, and introducing into the reaction vessel after silver halide grain nuclei have been formed and prior to introduction of at least 85 percent of the silver salt solution from 3 X 10-6 to 6 X 10-5 mole cadmium per mole of silver halide in the form of a water soluble cadmium salt.

24. In a process of forming a silver halide emulsion of the developing out type by a double-jet precipi-tation process in which an aqueous silver salt and at least one aqueous halide salt are separately and concurrently introduced into a reaction vessel in the presence of a gelatin or gelatin derived peptizer to form radiation-sensitive silver halide grains and surface chemically sensitizing the silver halide grains with a gold sensitizer, the improvement comprising forming silver halide grains which are at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, and introducing into the reaction vessel after silver halide grain nuclei have been formed and prior to introduction of at least 85 percent of the silver salt solution from 3 X 10-6 to 6 X 10-5 mole zinc per mole of silver halide in the form of a water soluble zinc salt.

25. In a process of forming a silver halide emulsion of the developing out type by a double-jet precipi-tation process in which an aqueous silver salt and at least one aqueous halide salt are separately and concurrently introduced into a reaction vessel in the presence of a gelatin or gelatin derived peptizer to form radiation-sensitive silver halide grains and surface chemically sensitizing the silver halide grains with a gold sensitizer, the improvement comprising forming silver halide grains which are at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, and introducing into the reaction vessel after silver halide grain nuclei have been formed and prior to introduction of at least 85 percent of the silver salt solution from 3 X
10-6 to 5 X 10-5 mole lead per mole of silver halide in the form of a water soluble lead salt.

26. In a process of forming a negative-working silver halide emulsion of the developing out type by a double-jet precipitation process in which an aqueous silver salt and at least one aqueous halide salt are separately and concurrently introduced into a reaction vessel in the presence of a gelatin or gelatin derived peptizer to form radiation-sensitive silver halide grains and surface chemically sensitizing the silver halide grains with a gold sensitizer, the improvement comprising forming silver halide grains which are at least 90 mole percent silver chloride and less than 2 mole percent silver iodide, based on total silver halide, and introducing into the reaction vessel after silver halide grain nuclei have been formed and prior to introduction of at least 85 percent of the silver salt solution from 3 X 10-6 to 5 X 10-5 mole copper per mole of silver halide in the form of a water soluble copper salt.

27. In a process according to claim 22, 23 or 24 the further improvement in which silver halide grains are formed which consist essentially of silver chloride.

28. In a process according to claim 25 or 26 the further improvement in which silver halide grains are formed which consist essentially of silver chloride.

29. In a process according to claim 22, 23 or 24 the further improvement in which a thioether or thiocyanate ripen-ing agent is present during formation of the silver halide grains.

30. In a process according to claim 25 or 26 the further improvement in which a thioether or thiocyanate ripening agent is present during formation of the silver halide grains.

31. In a process according to claim 22, 23 or 24 the further improvement in which the rates of addition of the water soluble silver and halide salts are controlled to produce a monodispersed silver halide emulsion.

32. In a process according to claim 25 or 25 the further improvement in which the rates of addition of the water soluble silver and halide salts are controlled to produced a monodispersed silver halide emulsion.