[0001] This invention relates to the field of photography. More particularly, the invention
is directed to improvements in radiation sensitive silver-halide emulsions.
[0002] In the late 1940's a transition in the manufacture of silver halide photographic
products began away from the use of single jet emulsions toward to the use of double
jet emulsions. The disadvantage of single jet emulsions was that they were polydisperse.
They contained a wide range of grain shapes and sizes. This was the direct result
of running silver salts into a halide salt solution of fixed volume in the reaction
vessel and thereby varying the ratio of silver to halide continuously throughout the
emulsion make.
[0003] In double jet precipitation both the halide and silver salts are concurrently introduced
into the reaction vessel. Thus, it is possible to produce a grain population of little
or no variance in grain shape and a very narrow distribution of grain sizes. Silver
halide emulsions having a low variance of grain sizes are referred to as monodisperse
emulsions.
[0004] Monodisperse emulsions are recognized to offer a variety of photographic advantages.
For example, a larger percentage of the grains in a monodisperse emulsion can be optimally
sensitized as a result of their similar surface areas. Fine grain populations, which
disproportionately contribute to light scattering and therefore image sharpness reduction,
are restricted. Larger grain populations, which contribute disproportionately to image
granularity, are restricted. The reproducibility of the emulsions and their photographic
performance rises as dispersity is reduced. Contrast of a single monodisperse emulsion
is higher than that of polydisperse emulsion of the same mean grain size. Monodisperse
emulsions are employed not only for photographic applications requiring higher contrast,
but are also blended to achieve aim contrasts in photographic applications requiring
relatively lower contrast, since a blended monodisperse emulsion retains photographic
advantages over a polydisperse emulsion of the same mean grain size and contrast.
[0005] Maternaghan U.S. Patents 4,150,994 and 4,184,878 are representative of early reported
attempts to prepare tabular grain silver bromoiodide emulsions. Covering power advantages
were postulated. Low coefficients of variation were reported for the emulsions. However,
in retrospect this is not surprising, since from remakes and grain characterizations
the average aspect ratios (most simply measured as mean grain diameter divided by
mean grain thickness) of these emulsions are approximately 4:1.
[0006] Subsequent to Maternaghan, intensive investigations of high aspect ratio silver bromoioide
emulsions were reported as well as procedures for their preparation. The average tabular
grain aspect ratios of these emulsions were in all instances greater than 8:1. Wilgus
et al U.S. Patent 4,434,226, Kofron et al U.S. Patent 4,439,520, Solberg et al U.S.
Patent 4,433,048, Daubendiek et al U.S. Patent 4,414,310, Jones et al U.S. Patent
4,478,929, Evans et al U.S. Patent 4,504,570, and Maskasky U.S. Patent 4,435,501 are
representative of the earliest published teachings relating to high aspect ratio silver
bromoiodide emulsions. More recently Daubendiek et al U.S. Patent 4,693,964 and 4,672,027
have reported the preparation of high aspect ratio silver bromoiodide emulsions of
much smaller mean grain diameters, referred to as small, thin tabular grain silver
bromoiodide emulsions. Maskasky U.S. Patent 4,713,320 illustrates the effect of gelatin
methionine reduction on silver bromoiodide high aspect ratio tabular grain emulsion
preparation.
[0007] The advantages of silver bromoiodide high aspect ratio tabular grain emulsions include
an improved relationship between speed and granularity, sharper images―both in single
and multilayer photographic elements, accelerated development, higher insensitivity
to temperature variations during development, higher fixing rates, more favorable
toning, higher covering power, an increased separation between minus blue (green or
red) and blue speeds when spectrally sensitized to the minus blue portion of the spectrum,
increased blue speed when spectrally sensitized to blue light, and a variety of other
advantages observed in the context of specific photographic applications.
[0008] Although almost all silver bromoiodide high aspect ratio tabular grain emulsions
are prepared by double jet precipitation techniques, difficulties were experienced
from the outset in reducing the dispersity of the emulsions. Whereas regular grain
emulsions produced by double jet precipitation (e.g., regular cubic or octahedral
grain emulsions) can be readily prepared containing only the desired grain population,
tabular grain emulsions are rarely prepared with only tabular grains present. Thus,
having mixed populations of tabular and nontabular grains is one source of dispersity
in tabular grain emulsions. The second source of dispersity is the dispersity variances
within the tabular grain population itself, which is a function of the twinning followed
by edge deposition growth pattern that distinguishes tabular grain emulsions from
regular grain emulsions, wherein twinning is absent or rare and deposition favors
no particular set of crystal faces. Further, dispersity in tabular grain emulsions
increases as the average aspect ratios of the tabular grains increases. Therefore,
dispersity levels which are easily attained in lower aspect ratio tabular grain emulsions
have not been attainable at higher aspect ratios.
[0009] Himmelwright U.S. Patent 4,477,565 and Sugimoto et al U.S. Patents 4,609,621, 4,656,120,
and 4,665,012 are illustrative of follow-on disclosures of variations in the preparation
of high aspect ratio tabular grain silver bromoiodide emulsions.
[0010] It has been recognized from the outset of high aspect ratio tabular grain emulsion
investigations that silver bromide tabular grain emulsions are much more readily
prepared to exhibit both high aspect ratios and low levels of dispersity than corresponding
silver bromoiodide emulsions.
Research Disclosure Vol. 232, Aug. 10, 1983, Item 23212, (Mignot French Patent 2,534,036 corresponding)
produced by a ripening procedure tabular grain silver bromide emulsions of average
aspect ratios of 10, 12, and 25.6 with coefficients of variation of 15, 16, and 28.4,
respectively.
Research Disclosure and its predecessor
Product Licensing Index are publications of Kenneth Mason Publications, Ltd., Emsworth, Hampshire P010 7DD,
England. Saitou et al West German OLS 3,707,135 A1 employs double and single jet precipitation
techniques to produce silver bromide emulsions which exhibit higher coefficients of
variation at aspect ratios comparable to those of Mignot, even though Saitou et al
reports coefficients of variations based solely on the tabular grain population.
[0011] It is an object of this invention to provide a high aspect ratio tabular grain emulsion
comprised of a dispersing medium and silver bromoiodide grains, wherein tabular silver
bromoiodide grains having a thickness of less than 0.3 µm account for greater than
50 percent of the projected area of the total silver bromoiodide grain population
and have an average aspect ratio of greater than 12 exhibit both the advantages of
high aspect ratio tabular grain silver bromoiodide emulsions and the art recognized
advantages of monodispersity.
[0012] The emulsion is characterized in that the quotient of the average silver bromoiodide
tabular grain aspect ratio divided by the coefficient of variation of the total silver
bromoiodide grain population is greater than 0.7.
[0013] Prior to the present invention it has been necessary to compromise either the average
tabular grain aspect ratio or the monodispersity of a silver bromoiodide emulsion.
With the present invention a superior relationship of grain dispersity and high tabular
grain aspect ratios is realized.
[0014] The present invention is an improvement on the teachings of Wilgus et al U.S. Patent
4,434,226, Kofron et al U.S. Patent 4,439,520, Solberg et al U.S. Patent 4,433,048,
Daubendiek et al U.S. Patent 4,414,310, 4,693,964 and 4,672,027, Evans et al U.S.
Patent 4,504,570, and Maskasky U.S. Patents 4,435,501 and 4,713,320. All features
of the emulsions of this invention, their preparation, and their photographic applications,
except as otherwise indicated, are to be understood as being as described by these
incorporated teachings.
[0015] The present invention is directed to silver bromoiodide tabular grain emulsions which
exhibit an improved relationship of grain tabularity to dispersity. A detailed discussion
requires more definitive terms.
[0016] As herein employed the term "high aspect ratio tabular grain emulsion" refers to
an emulsion in which the tabular grains having a thickness of less than 0.3 µm have
an average aspect ratio of greater than 12 and account for greater than 50% of the
total grain projected area. The average aspect ratio of the tabular grains can be
determined by determining the aspect ratio of each grain and averaging the aspect
ratios of all tabular grains or by dividing the average diameter of all of the tabular
grains by the average thickness of all the tabular grains.
[0017] The term "coefficient of variation" is employed in its art recognized sense as 100
times the standard deviation of all silver bromoiodide grain diameters divided by
the average silver bromoiodide grain diameter. All grains, including both tabular
and nontabular grains, are counted in arriving at averages. Defined in this way, the
coefficients of variation reported have higher numerical values than those based solely
on the tabular grain population.
[0018] When the average aspect ratio of the tabular silver bromoiodide grains of an emulsion
of this invention is divided by the coefficient of variation of all of the silver
bromoiodide grains present, a quotient of greater than 0.7 is obtained. This is a
significantly higher quotient than is exhibited by any silver bromoiodide tabular
grain emulsion heretofore known in the art. As shown in the examples below quotients
of greater than 0.7, 0.8 and 1.0 can be realized by emulsion preparation procedures
that have not been rigorously optimized. By routinely optimizing the emulsion preparation
techniques of the examples in view of the general teachings of this specification
it is recognized that quotients of 1.1, 1.5, 2.0, and higher are attainable.
[0019] The reason for defining the invention in terms of the quotient of the average aspect
ratio divided by the coefficient of variation rather than simply in terms of a minimum
coefficient of variation is that coefficients of variation increase linearly with
increases in the average aspect ratios of tabular grains using comparable processes
of emulsion preparation. For silver bromoiodide emulsions having average aspect ratios
in the 5:1 to 10:1 range monodispersities acceptable for present photographic performance
requirements are readily achieved. However, at average aspect ratios greater than
12:1 and beyond the art has an unsatisfied need for higher levels of monodispersity.
The present invention makes possible an improved balance of tabular grain average
aspect ratios and monodispersity in the aspect ratio ranges where satisfaction of
desired monodispersity have not been heretofore realized.
[0020] The preferred emulsions of the invention are those in which the tabular silver bromoiodide
grains having a thickness of less than 0.3 µm (optimally less than 0.2 µm) have an
average aspect ratio of greater than 12 (optimally at least 20). Very high average
aspect ratios ranging up to 100 or more are contemplated. In the preferred form of
the invention the tabular silver bromoiodide grains satisfying the thickness criteria
above account for greater than 70 percent (optimally greater than 90 percent) of the
total silver bromoiodide grain projected area. Ideally, of course, the emulsions of
the invention consist essentially of tabular silver bromoiodide grains satisfying
the thickness criteria above.
[0021] To satisfy normal photographic image definition requirements the mean grain size
(diameter) of the emulsions of this invention is less than 10 µm. While the invention
can be employed to produce very small diameter (0.2 to 0.6 µm mean diameter) tabular
grain emulsions, such as those disclosed by Daubendiek et al U.S. Patents 4,672,027
and 4,693,964, as well as those having mean tabular grain diameters above 0.6 µm,
the present invention has particular preferred applicability to emulsions having mean
grain diameters in the range of from 1.5 to 3.5 µm, particularly 1.5 to 2.5 µm.
[0022] The unique silver bromoiodide grain population required by the tabular grain emulsions
of this invention has resulted from replacing the empirical methods of emulsion preparation
disclosed in the art by a strategy for grain nucleation and growth specifically devised
to preserve monodispersity in the context of silver bromoiodide tabular grain precipitation.
[0023] The strategy begins with dividing the emulsion precipitation process into three distinct
stages:
(1) A nucleation stage in which all of the grains making up the emulsion come into
existence as separate entities. This stage is specifically managed to minimize variance
in the nuclei.
(2) A hold stage in which residual inequalities in grain nuclei are reduced.
(3) A growth stage in which residual inequalities in the grains, particularly at the
onset of the growth stage, can be further reduced. The growth stage is, of course,
controlled so that continued formation of grain nuclei does not occur.
[0024] While a variety of specific techniques are available for implementing the precipitation
strategies, not all are of equal importance nor are all required. It is a recognition
of this invention that grain variance elimination at the earliest possible opportunity
is of paramount importance, since an early grain variance has a cascading effect on
all subsequent stages of emulsion preparation.
[0025] The most important single process variation for achieving emulsions satisfying the
requirements of this invention is to implement a technique for as nearly concurrent
formation of all of the grain nuclei as possible. In an aqueous solution supersaturated
with silver and bromide ions precipitation occurs to produce a grain nucleus. This
nucleus immediately begins to grow. Unless all nuclei are concurrently formed, the
earlier formed nuclei will be larger than the initially formed nuclei. In the precipitation
processes demonstrated in the examples for preparing emulsions satisfying the requirements
of the invention the concentrations of the aqueous silver and bromide salts added
to the reaction vessel are increased and the duration of their addition is condensed
into a period of less than 10 seconds. Preferably both silver and bromide salt additions
are completed in less than 5 seconds and ideally in less than 1 second. To accomplish
this salt solution concentrations above 1 molar are preferred. This decreases the
bulk of the materials to be introduced. Since the aim is to drive the silver and bromide
ions out of solution as expeditiously as possible, temperature can be controlled to
limit solubility. Whereas precipitation temperatures are known to range up to 90°C,
it is preferred to limit temperatures at nucleation to 60°C or less. In summary, reducing
the elapsed time of initial silver and bromide salt additions is the most important
single process modification. Increasing salt concentrations and limiting temperature
are preferred features of nucleation. Finally, iodide ion is preferably omitted from
the nucleation stage to avoid unnecessarily complicating nucleation.
[0026] Upon creating the grains of the emulsion by nucleation, the next stage of the precipitation
strategy is to reverse immediately the initial direction of net ion transfer from
solution to nuclei, but in a controlled manner so that the majority of the nuclei
remain. This is achieved by abruptly moving from a supersaturated solution to a solution
which is below its silver and bromide ion saturation limit. The second stage is then
a ripening stage in which the smaller silver halide nuclei disappear while the remaining
nuclei remain. This can be achieved by employing any one or combination of known ripening
procedures. The simplest of these is to adjust upwardly the temperature of the nuclei
emulsion, thereby raising the solubility level of the silver and bromide ions. It
is also possible to increase the pBr of the solution while remaining within the growth
ranges taught in the art for silver bromoiodide tabular grain preparation. This lowers
the bromide ion concentration in solution and induces bromide ion migration back into
solution. It is a generally understood feature of ripening that smaller grains suffer
a net loss of silver and bromide ions while remaining grains exhibit a net increase.
As smaller grain nuclei are eliminated by ripening, the overall effect is to narrow
the grain size frequency distribution.
[0027] In the extreme instance in which nucleation is conducted in the absence of a peptizer
at room temperature the ripening can be conducted by raising the temperature up to
90°C, producing a temperature differential between nucleation and ripening of 70°C.
In practice significant improvements in emulsion characteristics are achieved when
the temperature differential between nucleation and ripening is in the range from
about 10 to 40°C, optimally about 15 to 30°C.
[0028] The duration of ripening in the second stage is preferably from 5 to 30 minutes in
the absence of a ripening agent other than the dissolved bromide ion. The addition
of known ripening agents, such as thioethers, thiocyanate, ammonia, and the like,
accelerate ripening. If ammonia is employed as a ripening agent, it is preferably
deactivated at the end of the ripening interval by an appropriate pH adjustment. The
nuclei ripening procedure of Nottorf U.S. Patent 4,722,886 is specifically contemplated.
[0029] This procedure alone, however, will not produce the emulsions of this invention.
[0030] At the end of the ripening stage a grain nuclei population is present which exhibits
less grain to grain variation than at the end of the nucleation step. It is now possible
to grow emulsions satisfying the requirements of this invention by employing conventional
silver bromoiodide tabular grain growth conditions, such as those set forth in the
teachings cited above.
[0031] Iodide ion is introduced in the growth stage. The teachings of Solberg et al U.S.
Patent 4,433,048 disclose preferred considerations for iodide addition.
[0032] It is preferred that the pBr of the reaction vessel during both the ripening and
growth stage be well above the pBr of the reaction vessel during nucleation. It is
generally preferred to adjust the pBr of the reaction vessel at the outset of the
ripening stage above 1.6 up to the growth stage pBr limits of the teachings cited
above. Further increase of the pBr will result in deposition onto the major faces
of the tabular grains and reduce the average aspect ratio of the emulsion.
[0033] Modifying compounds can be present during silver bromoiodide precipitation. Such
compounds can be initially in the reaction vessel or can be added along with one or
more of the salts according to conventional procedures. Modifying compounds, such
as compounds of copper, thallium, lead, bismuth, cadmium, zinc, middle chalcogens
(i.e., sulfur, selenium and tellurium), gold., and Group VIII noble metals, can be
present during precipitation, as illustrated by Arnold et al U.S. Patent 1,195,432,
Hochstetter U.S. Patent 1,951,933, Trivelli et al U.S. Patent 2,448,060, Overman U.S.
Patent 2,628,167, Mueller et al U.S. Patent 2,950,972, Sidebotham U.S. Patent 3,488,709,
Rosecrants et al U.S. Patent 3,737,313, Berry et al U.S. Patent 3,772,031, Atwell
U.S. Patent 4,269,927, and
Research Disclosure, Vol. 134, June 1975, Item 13452. The tabular grain emulsions can be internally reduction
sensitized during precipitation, as illustrated by Moisar et al,
Journal of Photographic Science, Vol. 25, 1977, pp. 19-27.
[0034] Once the silver bromoiodide high aspect ratio tabular grain emulsions have been formed
by the process of the present invention they can be shelled to produce a core-shell
emulsion by procedures well known to those skilled in the art. Any photographically
useful silver salt can be employed in forming shells on the high aspect ratio tabular
grain emulsions prepared by the present process. Techniques for forming silver salt
shells are illustrated by Evams et al U.S. Patent 4,504,570.
[0035] In forming the tabular grain emulsions peptizer concentrations of from 0.2 to about
10 percent by weight, based on the total weight of emulsion components in the reaction
vessel, can be employed. It is common practice to maintain the concentration of the
peptizer in the reaction vessel in the range of below about 6 percent, based on the
total weight, prior to and during grain formation and to adjust the emulsion vehicle
concentration upwardly for optimum coating characteristics by delayed, supplemental
vehicle additions. It is contemplated that the emulsion as initially formed will contain
from about 5 to 50 grams of peptizer per mole of silver halide, preferably about 10
to 30 grams of peptizer per mole of silver halide. Additional vehicle can be added
later to bring the concentration up to as high as 1000 grams per mole of silver halide.
Preferably the concentration of vehicle in the finished emulsion is above 50 grams
per mole of silver halide. When coated and dried in forming a photographic element
the vehicle preferably forms about 30 to 70 percent by weight of the emulsion layer.
[0036] Vehicles (which include both binders and peptizers) can be chosen from among those
conventionally employed in silver halide emulsions. Preferred peptizers are hydrophilic
colloids, which can be employed alone or in combination with hydrophobic materials.
Suitable hydrophilic materials include substances such as proteins, protein derivatives,
cellulose derivatives―e.g., cellulose esters, gelatine―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 derivatives, agar-agar, arrowroot, albumin
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 3,061,436, 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 3,539,353, Miller et al U.S. Patent 3,227,571, Boyer et al U.S. Patent
3,532,502, 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, Hori et al U.K. Patent 1,489,080 and Belgian Patent 856,631,
U.K. Patent 1,490,644, UK. 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
2,323,085, 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 1,752,069, 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.
[0037] When silver bromoiodide high aspect ratio tabular grain emulsions according to the
invention are being prepared in which the mean tabular grain thickness is less than
about 0.07 µm, particularly less than 0.05 µm, it is preferred to employ gelatin and
gelatin derived peptizers containing less than 30 micromoles per gram methionine.
The methionine content can be reduced by treatment of the peptizer with an oxidizing
agent, such as hydrogen peroxide. The teachings of Daubendiek et al U.S. Patents 4,672,027
and 4,693,964 are particularly applicable. Although not essential, the reduction or
elimination of methionine from the peptizer facilitates achieving very thin tabular
grain structures.
[0038] Other materials commonly employed in combination with hydrophilic colloid peptizers
as vehicles (including vehicle extenders―e.g., materials in the form of latices) 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 pyridine, acrylic acid polymers, maleic anhydride copolymers,
polyalkylene oxides methacrylamide copolymers, polyvinyl oxazolidinones, maleic acid
copolymers, vinylamine copolymers, methacrylic acid copolymers, acryloyloxyalkylsulfonic
acid copolymers, sulfoalkylacrylamide copolymers, polyalkyleneimine copolymers, polyamines,
N,N-dialkylaminoalkyl acrylates, vinyl imidazole copolymers, vinyl sulfide copolymers,
halogenated styrene polymers, amineacrylamide polymers, polypeptides and the like
as described in Hollister et al U.S. Patents 3,679,425, 3,706,564 and 3,813,251, Lowe
U.S. Patents 2,253,078, 2,276,322, '323, 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 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 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 3,003,879, 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 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 Canadian Patent 774,054, Ream et al U.S. Patent 3,287,289, Smith U.K.
Patent 1,466,600, Stevens U.K. Patent 1,062,116, 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 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. 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 precipitation, but rather are conventionally added to
the emulsion prior to coating. The vehicle materials, including particularly the hydrophilic
colloids, as well as the hydrophobic materials useful in combination therewith can
be employed not only in the emulsion layers of photographic elements, but also in
other layers, such as overcoat layers, interlayers and layers positioned beneath the
emulsion layers.
[0039] As discussed above, ripening can occur during the hold stage of emulsion preparation.
However, ripening need not and commonly is not confined to just this one stage of
emulsion preparation. Known silver halide solvents are useful in promoting ripening.
For example, an excess of bromide ions, when present in the reaction vessel, is known
to promote ripening. It is therefore apparent that the bromide salt solution run into
the reaction vessel can itself promote ripening. Other ripening agents can also be
employed and can be entirely contained within the dispersing medium in the reaction
vessel before silver and halide salt addition, or they can be 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.
[0040] Among preferred ripening agents are those containing sulfur. Thiocyanate salts can
be used, such as alkali metal, most commonly sodium and 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. Illustrative prior teachings of employing thiocyanate ripening
agents are found in Nietz et al, U.S. Patent 2,222,264, cited above; Lowe et al U.S.
Patent 2,448,534 and Illingsworth U.S. Patent 3,320,069. Alternatively, conventional
thioether ripening agents, such as those disclosed in McBride U.S. Patent 3,271,157,
Jones U.S. Patent 3,574,628, and Rosecrants et al U.S. Patent 3,737,313.
[0041] The silver bromoiodide high aspect ratio tabular grain emulsions of the present invention
are preferably washed to remove soluble salts. Conventional washing procedures, such
as those disclosed in
Research Disclosure, Vol. 176, Dec. 1978, Paragraph II are contemplated.
[0042] In accordance with established practices within the art it is specifically contemplated
to blend the high aspect ratio tabular grain emulsions prepared by the process of
the present invention with each other or with conventional emulsions to satisfy specific
emulsion requirements. For example, it is known to blend emulsions to adjust the characteristic
curve of a photographic element to satisfy a predetermined aim. Blending can be employed
to increase or decrease maximum densities realized on exposure and processing, to
decrease or increase minimum density, and to adjust characteristic curve shape between
its toe and shoulder. To accomplish this the emulsions of this invention can be blended
with conventional silver halide emulsions, such as those described in
Research Disclosure, Item 17643, cited above, Paragraph 1. When a relatively fine grain silver chloride
emulsion is blended with the silver bromoiodide emulsions of the present invention,
a further increase in the sensitivity―i.e., speed-granularity relationship―of the
emulsion can result.
[0043] Once silver bromoiodide high aspect ratio tabular grain emulsions have been prepared
by the process of the present invention, they can be further modified, coated, exposed,
and processed following procedures well known to those skilled in the art.
[0044] The emulsions prepared by the present process can be chemically sensitized, as described
in
Research Disclosure, Item 17643, cited above, Paragraph III. The emulsions can be spectrally sensitized
and/or desensitized, as described in Paragraph IV. It is specifically prefer- red
to substantially optimally chemically and spec- trally sensitize the emulsions prepared
by the present process by the techniques disclosed in Kofron et al, and Maskasky U.S.
Patent 4,435,501, cited above.
[0045] The photographic emulsions can contain brighteners, antifoggants, stabilizers, scattering
or absorbing materials, hardeners, coating aids, plasticizers, lubricants, and matting
agents, as described in Item 17643, Paragraphs V, VI, VIII, X, XI, XII, and XVI. Methods
of addition and coating and drying procedures can be employed, as described in Paragraphs
XIV and XV. Conventional photographic supports can be employed, as described in Paragraph
XVII. The photographic elements produced can be black-and-white or, preferably, color
photographic elements which form silver images and/or dye images through the selective
destruction, formation, or physical removal of dyes, as described in Paragraph VII.
Specifically preferred color photographic elements are those which form dye images
through the use of color developing agents and dye-forming couplers. To put the photographic
elements to use, they can be conventionally exposed, as described in Paragraph XVIII,
and they can be conventionally processed, as described in Paragraph XIX.
Examples
[0046] The invention can be better appreciated by reference to the following specific examples.
[0047] In each of the examples the contents of the reaction vessel were stirred vigorously
throughout silver and halide salt introductions; the term "percent" means percent
by weight, unless otherwise indicated; and the term "M" stands for molar concentration,
unless otherwise indicated. All solutions, unless otherwise indicated are aqueous
solutions.
Emulsion 1 (Control)
[0048] The following is representative of type of silver bromoiodide high aspect ratio tabular
grain emulsion on which the art is now relying for the highest achievable photographic
performance.
[0049] To 1.5 liters of a 0.25 percent gelatin solution containing 0.05M sodium bromide
at 50°C, pH 5.8, was added with vigorous stirring 0.12M silver nitrate solution over
a 2.0 minute period (consuming 0.55 percent of the total silver used). The temperature
was then raised to 70°C over four minutes and held at 70°C for a further six minutes.
One and one half liters of aqueous gelatin solution (4.3 percent by weight) were added
to the reaction vessel. The pBr within the reaction vessel was then adjusted to 1.13
at 70°C. A halide solution containing sodium bromide (1.89M) plus potassium iodide
(0.06M) and a 1.50M silver nitrate solution were added by double jet addition utilizing
accelerated flow (7 X increase in flow rates from start to finish) for 40 minutes
at pBr 1.13 at 70°C, consuming 99.45 percent of the total silver used. Approximately
2.2 moles of silver were used to prepare this emulsion.
[0050] The resultant silver bromoiodide high aspect ratio tabular grain emulsion had an
average grain diameter of 2.17 µm, an average tabular grain thickness of 0.08 µm,
an average aspect ratio of 27, and a coefficient of variation, based on the total
grain population, of 69. Tabular grains accounted for 85% of the total grain projected
area.
[0051] The quotient of the average aspect ratio divided by coefficient of variation was
0.4. This demonstrates a conventional relationship between tabularity (average aspect
ratio) and dispersity (coefficient of variation). It is a significantly worse relationship
(lower quotient) than is achieved by the present invention.
Emulsion 2 (Invention)
[0052] To 1.5 liters of a 0.25 percent gelatin solution containing 0.05M sodium bromide
at 50°C, pH 5.8, was added with vigorous stirring 4 mL of 3M silver nitrate solution
over a 2 second period (consuming 0.55 percent of the total silver used). The temperature
was then raised to 70°C over four minutes and held at 70°C for a further six minutes.
One and one half liters of aqueous gelatin solution (4.3 percent by weight) were added
to the reaction vessel. The pBr within the reaction vessel was then adjusted to 1.78
at 70°C. A halide solution containing sodium bromide (1.89M) plus potassium iodide
(0.06M) and a 1.5M silver nitrate solution were added by double jet addition utilizing
accelerated flow (14 X increase in flow rates from start to finish) for 42 minutes
at pBr 1.78 at 70°C, consuming 99.45 percent of the total silver used. Approximately
2.2 moles of silver were used to prepare this emulsion.
[0053] The resultant silver bromoiodide high aspect ratio tabular grain emulsion had an
average grain diameter of 1.78 µm, an average tabular grain thickness of 0.08 µm,
an average aspect ratio of 22, and a coefficient of variation, based on the total
grain population, of 29. Tabular grains accounted for 85% of the total grain projected
area.
[0054] The quotient of the average aspect ratio divided by coefficient of variation was
0.76. This demonstrates a significant improvement in the relationship between tabularity
(average aspect ratio) and dispersity (coefficient of variation). It is a significantly
better relationship (higher quotient) than was achieved using the comparable conventional
emulsion preparation technique of control Emulsion 1.
Emulsion 3 (Invention)
[0055] To 1.5 liters of a 0.25 percent gelatin solution containing 0.05M sodium bromide
at 50°C, pH 5.8, was added with vigorous stirring 4 mL of 3M silver nitrate solution
over a 2 second period (consuming 0.55 percent of the total silver used). The temperature
was then raised to 70°C over four minutes. To the reaction vessel was then added 0.17
millimole of 1,10-dithia-4,7,13,16-tetraoxacyclooctadecane. The reaction vessel was
held at 70°C for a further six minutes. One and one half liters of aqueous gelatin
solution (4.3 percent by weight) were added to the reaction vessel. The pBr within
the reaction vessel was then adjusted to 1.78 at 70°C. A halide solution containing
sodium bromide (1.89M) plus potassium iodide (0.06M) and a 1.5M silver nitrate solution
were added by double jet addition utilizing accelerated flow (14 X increase in flow
rates from start to finish) for 42 minutes at pBr 1.78 at 70°C, consuming 99.45 percent
of the total silver used. Approximately 2.2 moles of silver were used to prepare this
emulsion.
[0056] The resultant silver bromoiodide high aspect ratio tabular grain emulsion had an
average grain diameter of 2.35 µm, an average tabular grain thickness of 0.12 µm,
an average aspect ratio of 20, and a coefficient of variation, based on the total
grain population, of 23. Tabular grains accounted for 88% of the total grain projected
area.
[0057] The quotient of the average aspect ratio divided by coefficient of variation was
0.87. This demonstrates a significant improvement in the relationship between tabularity
(average aspect ratio) and dispersity (coefficient of variation). It is a significantly
better relationship (higher quotient) than was achieved using the comparable conventional
emulsion preparation technique of control Emulsion 1.
[0058] Comparing Emulsions 2 and 3, it is apparent that the addition of the thioether ripening
agent caused the tabular grains to grow larger in diameter and somewhat thicker by
ripening out a higher proportion of smaller grains, reflected in the increased percentage
of the total grain projected area accounted for by the tabular grains. While the ripening
agent actually lowered the average tabular grain aspect ratio slightly, it reduced
the coefficient by a relatively much larger amount, thereby raising the quotient,
indicating an overall improved relationship of tabularity and dispersity in the direction
of ideal monodispersity.
Emulsion 4 (Control)
[0059] This emulsion is neither a conventional emulsion or an example of the invention.
It is an in-between emulsion offered to shed light on the question suggested by a
comparison of Emulsions 2 and 3 as to whether reliance on the thioether ripening agent
without concurrent reliance on accelerated nucleation would produce an emulsion satisfying
the tabularity to dispersity requirement of this invention.
[0060] To 1.5 liters of a 0.25 percent gelatin solution containing 0.05M sodium bromide
at 50°C, pH 5.8, was added with vigorous stirring 0.12M silver nitrate solution over
a 2.0 minute period (consuming 0.55 percent of the total silver used). The temperature
was then raised to 70°C over four minutes. To the reaction vessel was then added 0.08
millimole of 1,10-dithia-4,7,13,16-tetraoxacyclooctadecane The reaction vessel was
held at 70°C for a further six minutes. One and one half liters of aqueous gelatin
solution (4.3 percent by weight) were added to the reaction vessel. The pBr within
the reaction vessel was then adjusted to 1.78 at 70°C. A halide solution containing
sodium bromide (1.89M) plus potassium iodide (0.06M) and a 1.5M silver nitrate solution
were added by double jet addition utilizing accelerated flow (7 X increase in flow
rates from start to finish) for 40 minutes at pBr 1.78 at 70°C, consuming 99.45 percent
of the total silver used. Approximately 2.2 moles of silver were used to prepare this
emulsion.
[0061] The resultant silver bromoiodide high aspect ratio tabular grain emulsion had an
average grain diameter of 1.77 µm, an average tabular grain thickness of 0.09 µm,
an average aspect ratio of 20, and a coefficient of variation of 31. Tabular grains
accounted for 88% of the total grain projected area.
[0062] The quotient of the average aspect ratio divided by coefficient of variation was
0.65. From this data it appears that the slower nucleation produced a dispersity in
the grain nuclei that could not be overcome by subsequent ripening. It appears that
the ripening agent ripened out about the same proportion of nontabular grains, but
the slower nucleation resulted in a significantly higher dispersity within the tabular
grain population.
Emulsion 5 (Invention)
[0063] This emulsion is offered to illustrate the formation of a silver bromoiodide high
aspect ratio tabular grain emulsion according to the invention having a mean grain
thickness of less than 0.05 µm, facilitated by the use of gelatin peptizer treated
with an oxidizing agent to eliminate methionine.
[0064] To an 18 liter stainless steel reaction vessel was added. with vigorous stirring
6.0 liters of 0.125 percent oxidizing agent treated (less than 30 micromoles per gram
residual unoxidized methionine) gelatin solution containing 0.04 moles of sodium bromide
at 45°C with the pH adjusted to 1.85 using sulfuric acid. To this solution was added
8.0 mL of 1.67M silver nitrate along with 8.0 mL of 1.6M halide solution consisting
of 98.5 mole percent sodium bromide and 1.5 mole percent potassium iodide by balanced
double jet addition at 120 mL per minute. The temperature was then raised to 60°C
over 9 minutes and held for an additional 9 minutes. This was followed by the addition
of 100g of the oxidizing agent treated gelatin and a pH adjustment to 5.85 using 2.5M
sodium hydroxide. The pBr was then adjusted to 1.75 using a 1.0M sodium bromide for
40 minutes at 12.5 mL per minute with the pBr maintained at 1.75. The solution addition
was then stopped for 90 seconds while the pBr was adjusted to 1.55 using the 175M
sodium bromide solution. This was followed by a triple jet addition of 1.6M silver
nitrate, 0.048M silver iodide Lippmann emulsion suspension, and 1.75M sodium bromide
solution. The triple jet addition of the same solutions previously described was then
continued with a linearly accelerated flow rate from 12.5 mL per minute to 120 mL
per minute. This yielded 6 moles of a silver bromoiodide very thin tabular grain emulsion,
which was coagulation washed by the procedure of Yutzy et al U.S. Patent 2,614,929.
[0065] The resultant silver bromoiodide high aspect ratio tabular grain emulsion had an
average grain diameter of 2.9 µm, an average tabular grain thickness of 0.04 µm, an
average aspect ratio of 72, and a coefficient of variation, based on the total grain
population, of 56.
[0066] The quotient of the average aspect ratio divided by coefficient of variation was
1.3. From this data it appears that the reduction in the thickness of the tabular
grains resulted in a large increase in projected area that more than offset a modest
rise in the coefficient of variation, which was an expected result of increasing the
mean grain diameter of the emulsion.
Emulsion 6 (Invention)
[0067] Because of the very favorable relationship of tabularity and dispersity achieved
by the Emulsion 5, it was possible to substitute a single jet nucleation for the double
jet nucleation employed in the preparation of Emulsion 5 while still obtaining a silver
bromoiodide high aspect ratio tabular grain emulsion having a quotient of average
aspect ratio divided by coefficient of variation well in excess of 0.7.
[0068] The initial solution before nucleation was prepared as described for Emulsion 5.
The balanced double jet nucleation employed for Emulsion 5 was replaced by a single
jet nucleation consisting of 8.0 mL of 1.67M silver nitrate solution delivered at
approximately 5000 mL per minute. This was immediately followed by a temperature rise,
hold time, gelatin addition, pH and pBr adjustments, and an initial constant flow
rate triple jet addition that were identical to that of Emulsion 5. The pBr adjustment
to 1.55 of Emulsion 5 was replaced with a pBr adjustment to 1.85 using the 1.6M silver
nitrate solution. The final ramped flow rate triple jet addition was identical to
that of Emulsion 5, except that the pBr was controlled at 1.85.
[0069] The resultant silver bromoiodide high aspect ratio tabular grain emulsion had bin
average grain diameter of 2.3 µm, an average tabular grain thickness of 0.045 µm,
an average aspect ratio of 51, and a coefficient of variation, based on the total
grain population, of 43.
[0070] The quotient of the average aspect ratio divided by coefficient of variation was
1.2.
Emulsion 7 (Invention)
[0071] This emulsion is offered to illustrate the formation of a silver bromoiodide high
aspect ratio tabular grain emulsion according to the invention wherein silver iodide
was abruptly added as a Lippmann emulsion during grain growth.
[0072] To an 18 liter stainless steel reaction vessel was added with vigorous stirring 6.0
liters of 0.125 percent oxidizing agent treated (less than 30 micromoles per gram
residual unoxidized methionine) gelatin solution containing 0.04 moles of sodium bromide
at 4506 with the pH adjusted to 1.85 using sulfuric acid. To this solution was added
8.0 mL of 1.67M silver nitrate along with 8.0 mL of 1.6M halide solution consisting
of 98.5 mole percent sodium bromide and 1.5 mole percent potassium iodide by balanced
double jet addition at 120 mL per minute. After 60 seconds the pBr was adjusted to
1.73 by the addition of 1.0M sodium bromide. The temperature was then raised to 60°C
over 9 minutes and held for an additional 9 minutes. This was followed by the addition
of 100g of the oxidizing agent treated gelatin and a pH adjustment to 5.85 using 2.5M
sodium hydroxide. The triple jet addition of 1.6M silver nitrate, 0.024M silver iodide
Lippmann emulsion suspension, and 1.75M sodium bromide solution was then run at 12.5
mL per minute for 40 minutes with the pBr controlled at 1.83. The triple jet addition
was then continued with a linearly accelerated flow rate from 12.5 mL per minute to
120 mL per minute over 35.8 minutes. The addition was then stopped and 0.12 moles
of silver iodide Lippmann were added. A double jet additon of 1.6M silver nitrate
and 1.75M sodium bromide was then run at 100 mL per minute for 3.65 minutes with pBr
controlled at 1.83. This yielded 6 moles of a silver bromoiodide very thin tabular
grain emulsion, which was coagulation washed by the procedure of Yutzy et al U.S.
Patent 2,614,929.
[0073] The resultant silver bromoiodide high aspect ratio tabular grain emulsion contained
over 90 percent tabular grains, had an average grain diameter of 2.85 µm, an average
tabular grain thickness of 0.06 µm, an average aspect ratio of 47.5, and a coefficient
of variation, based on the total grain population, of 38.
[0074] The quotient of the average aspect ratio divided by coefficient of variation was
1.25. From this data it is apparent that the addition of silver iodide during the
growth stage of tabular grain formation as a Lippmann emulsion suspension is entirely
compatible with obtaining a high quotient of average aspect ratio divided by the coefficient
of variation.
[0075] Taken as a whole the examples suggest that once the overall strategy for preparing
a silver bromoiodide high aspect ratio tabular grain emulsion having a favorable relationship
of tabularity and dispersity (a high quotient of the average aspect ratio divided
by the coefficient of variation) is appreciated from the discussion above in the specification,
the desired emulsions can be realized with some freedom in selection of individual
preparation parameters, not all of which are of equal importance. It is therefore
apparent that variant procedures will occur to those skilled in the art having access
to the teachings of this invention.
[0076] The invention has been described in terms of coefficients of variation of grain diameters.
Since nontabular grain populations exhibit diameters based on their projected areas
that are essentially the same as their thickness, the art has not yet addressed the
coefficients of variation for tabular grain emulsions based on variations in tabular
grain thicknesses as opposed to variations in tabular grain diameter (the diameter
of a circle having the same projected area as the tabular grain). Measurements of
tabular grain thickness variation are of necessity somewhat more difficult to generate,
since tabular grain thicknesses are much smaller than tabular grain diameters and
mist be determined indirectly by shadow length measurements of carbon grain replicas.
Nevertheless, analysis of this type has been performed, and it has been determined
that the emulsion preparation strategies and specific techniques herein disclosed
are also effective to reduce variations in tabular grain thicknesses. Although differences
in thickness from one tabular grain to the next are in many instances small, even
small differences can have a significant impact on varying the surface area to volume
ratio of a tabular grain population.