FIELD OF THE INVENTION
[0001] The present invention relates to a photosensitive silver halide material for obtaining
black-and-white half-tone, dot or line, images having improved resistance to pressure
desensitization.
BACKGROUND OF THE ART
[0002] Photosensitive silver halide materials are commonly used in photolithographic industry
to obtain half-tone, dot or line, high contrast images. An example of high contrast
photographic element having white reflective support is a phototypesetting material
intended to produce black type character image on a white background. An example of
high contrast photographic element having a transparent support is lith film, so called
because it is used as contact transparency for exposing lithographic printing plates.
The illusion that some areas of a printed image are of intermediate density is created
by the viewer's inability to resolve tiny dots or lines of maximum density and background
areas of minimum density that separate them. Such images are referred to as half-tone
images.
[0003] It is known in the art of silver halide photography that unevenly applied pressure
can result in localized differences in density over the photographic film. This is
an adverse effect for ractical applications, and is known as pressure or kink sensitivity.
According to this effect a part of a light-sensitive silver halide photographic material
ecomes spuriously black or white by sensitization or by desensitization. In some instances
the density produced by the silver halide grains is increased, but more commonly the
silver halide grains are desensitized. Pressure sensitization or desensitization occur
during handling of the photographic material (i.e., by folding, twisting and/or warping)
or during roller transport processing. Pressure desensitization has been most often
observed in large format photographic elements, which are more susceptible to kinking.
[0004] Pressure sensitivity of the silver halide photographic material can be reduced by
the incorporation of various addenda, such as, for example, the addenda described
in
Research Disclosure, Vol 176, December 1978, Item 17643, Section VI, K ;
Research Disclosure, Vol 184, August 1979, Item 18431, Section II, H;
Research Disclosure, Vol 308, December 1989, Item 308,119, Section VI, K-L; and E.J.Birr, Stabilization
of Silver Halide Emulsion, Focal Press, London, 1974, pp. 133-134.
Research Disclosure is published by Kenneth Mason Publications, Ltd., Emsworth, Hampshire P010 7DD, England.
However, such addenda often affect photographic characteristics without having a substantial
effect on pressure sensitivity.
[0005] The incorporation of substituted or unsubstituted polyhydroxybenzenes in silver halide
photographic material to reduce pressure sensitivity is disclosed in EP 209,010, claiming
a negative working photographic material of high contrast and reduced pressure sensitivity,
which comprises polyhydroxybenzenes and arylhydrazides, US 4,914,002, claims a silver
halide photographic material with excellent pressure properties, which contains a
combination of hydrazine derivatives, cyanine derivatives having no absorption maximum
in the visible light region and dihydroxybenzene derivatives.
[0006] However, the use of polyhydroxybenzene to reduce pressure sensitivity is limited
in that the high quantity of said compound can deteriorate anti-blocking properties,
in particular, it can increase the tendency toward tackiness of the emulsion.
[0007] Accordingly, there is still the need for a silver halide photographic material which
reduces all the above mentioned problems.
SUMMARY OF THE INVENTION
[0008] The present invention relates to a light-sensitive silver halide photographic material
to obtain black-and-white half-tone, dot or line, images comprising a support and
coated thereon one or more hydrophilic layers, at least one of said hydrophilic layers
including a high chloride content silver halide emulsion, characterized in that said
silver halide emulsion comprises a polyhydroxybenzene having the following formula:

wherein n is 1,2 or 3,
and in that the outermost hydrophilic layer comprises a polydialkylsiloxane.
[0009] Preferably, said polydialkylsiloxane corresponds to the following formula:

wherein R₁ is an alkyl group having 1 to 3 carbon atoms, R₂ is an alkyl group having
1 to 3 carbon atoms or an alkoxy group having 1 to 2 carbon atoms and n is a positive
integer of from 0 to 2000.
[0010] In a further aspect the present invention relates to a method for obtaining a half-tone,
dot or line, image, wherein a silver halide photographic material, comprising a support
and coated thereon one or more hydrophilic layers, at least one of said hydrophilic
layers including a high chloride content silver halide emulsion, is image-wise exposed
for forming said image, and subjected to a photographic process comprising an alkaline
developing solution, characterized in that the high-chloride content silver halide
emulsion of said photographic material comprises a polyhydroxybenzene derivative of
formula

wherein n is 1,2 or 3,
and in that the outermost hydrophilic layer of said photographic material comprises
a polydilakylsiloxane preferably having the following formula:

wherein R₁ is an alkyl group having 1 to 3 carbon atoms, R₂ is an alkyl group having
1 to 3 carbon atoms or an alkoxy group having 1 to 2 carbon atoms and n is a positive
integer of from 0 to 2000.
DETAILED DESCRIPTION OF THE INVENTION
[0011] The present invention relates to a light-sensitive silver halide photographic material
to obtain black-and-white half-tone, dot or line, images comprising a support and
coated thereon one or more hydrophilic layers, at least one of said hydrophilic layers
including a high chloride content silver halide emulsion, characterized in that said
silver halide emulsion comprises a polyhydroxybenzene having the following formula:

wherein n is 1,2 or 3,
and in that the outermost hydrophilic layer comprises a polydilakylsiloxane preferably
having the following formula:

wherein R₁ is an alkyl group having 1 to 3 carbon atoms, R₂ is an alkyl group having
1 to 3 carbon atoms or an alkoxy group having 1 to 2 carbon atoms and n is a positive
integer of from 0 to 2000.
[0012] The polyhydroxybenzenes according formula (I) above can be dihydroxybenzene derivatives,
trihydroxybenzene derivatives, or tetrahydroxybenzene derivatives. Useful examples
of dihydroxybenzene are 1,2-dihydroxybenzene, i.e., pyrocatechol, 1,3-dihydroxybenzene,
i.e., resorcinol, 1,4-dihydroxybenzene, i.e., hydroquinone. Useful examples of trihydroxybenzene
are 1,2,3-trihydroxybenzene, i.e., pyrogallol, 1,3,5-trihydroxybenzene, i.e., phloroglucinol,
1,2,4-trihydroxybenzene, i.e., hydroxyhydroquinone. Useful examples of tetrahydroxybenzene
are 1,2,3,4-tetrahydroxybenzene, 1,2,4,5-tetrahydroxybenzene, 1,3,4,5-tetrahydroxybenzene.
[0013] Said polyhydroxybenzenes can be unsubstituted or substituted with, for example, halogen,
alkyl, alkoxy, amino, amido, sulfonamido, carboxy, and the like. Unsubstituted polyhydroxybenzenes
are preferred.
[0014] The polyhydroxybenzenes are added to the photographic emulsion comprising light sensitive
silver halide grains and a carrying medium or binder in an amount of from 0.01 to
0.1 moles per mole of silver, preferably of from 0.03 to 0.07 moles per mole of silver.
[0015] The polydialkylsiloxanes according to the formula (II) above are generally added
to the carrying medium or binder which forms the outermost layer of the film as an
aqueous dispersion in the presence of a suitable dispersing agent, preferably a non-ionic
dispersing agent. An aqueous dispersion containing 35% by weight of the silicone polymer
is preferred but dispersions containing 1 to 50% by weight of the polymer are suitable.
[0016] Useful polydialkylsiloxanes include commercially available silicone oils such as
the trialkyl and trialkoxy endblocked dialkylpolysiloxanes, e.g., dimethylpolysiloxane,
diethylpolysiloxane, trimethoxy endblocked dimethylpolysiloxane and triethoxy endblocked
dimethylpolysiloxane. The polydialkylsiloxanes have molecular weights of from 100
to 150,000, preferably of from 10,000 to 20,000 and a viscosity at 25°C of from 2
to 100,000 centistokes, preferably of from 200 to 800 centistokes.
[0017] The preparation and properties of such polydialkylsiloxanes are well known and described,
for instance, in Reuben Gutoff's article entitled "
Silicone Fluid Manufacture", published in "
Industrial and Engineering Chemistry", Vol 49, pp 1807-1811.
[0018] The polydialkylsiloxanes can be used in any concentration which is effective for
the intended purpose. A suitable concentration is of from 0.01 to 0.1, preferably
of from 0.02 to 0.08 grams per square meter of the photographic material.
[0019] Suitable dispersing agents are generally of non-ionic type such as alkyl phenyl polyethylene
glycol ethers, e.g., nonyl phenyl polyethylene glycol ether, and undecyl phenyl polyethylene
glycol ether; alkyl and aralkyl polyether alcohols, e.g., iso-octyl phenyl polyethoxyethanol,
nonyl phenyl polyethoxyethanol, and tetradecyl phenyl polyethoxyethanol. Other suitable
dispersing agents include saponin and the oxyalkylene ethers of hexitol ring dehydration
products, e.g., the polyoxyethylene sorbitan monolaurates, monostearates and monooleates
which contain 2 to 20 oxyethylene groups divided in three chains; salts of alkyl-substituted
aryloxy alkylene ether sulfonates, e.g., sodium p-t-octylphenoxyethoxyethyl sulfonate;
sodium dodecyl, tetradecyl and octadecyl sulfates and the dioctyl ester of sodium
sulfosuccinic acid. Certain soaps, e.g., morpholine oleate and sodium stearate, can
also be used. The dispersing agents are used in amount of from 1 to 50%, preferably
of from 2 to 20% by weight of the silicone oil.
[0020] Instead of being added as a dispersion, the polydialkylsioloxanes can be added in
a suitable organic solvent, e.g., amyl acetate, benzene, carbon tetrachloride, ethyl
ether, perchloroethylene, petroleum ether, or xylene. The organic solvent, of course,
must not adversely affect the physical or photographic properties of the photographic
film.
[0021] As a vehicle or binder for the hydrophilic layer of the photographic material of
the present invention, any hydrophilic binder known in the art can be used. Suitable
binders include natural polymers, synthetic resins, polymers and copolymers, and other
film forming media. The binders may range from thermoplastic to highly cross-linked,
and may be coated from aqueous or organic solvents or emulsions.
[0022] Gelatin is the preferred hydrophilic colloid for use in the present invention. However,
other water-soluble colloidal substances or mixtures thereof can also be used. Exemplary
hydrophilic colloidal substances include gelatine derivatives, such as phthalated
gelatin and acetylated gelatine, cellulose derivatives, such as carboxymethyl cellulose,
starch, casein, zein, synthetic hydrophilic colloids such as polyvinyl alcohol, polyvinyl
pyrrolidone, copolymers of acrylic acid esters, acrylonitrile and acrylamides, etc.
[0023] The amount of hydrophilic binder used in practice depends on the dispersing solvent
amount and the coating thickness required. Since an excessive amount of binder can
reduce maximum density and contrast, for the purpose of the present invention, the
binder is advantageously used in an amount lower than 250 grams per mole of silver
halide, preferably in an amount of from 20 to 200 grams per mole of silver halide.
[0024] The silver halide emulsions used in the present invention are preferably monodispersed,
but emulsions having a wide grain size distribution can also be used. The term "monodispersed"
refers to an emulsion having a coefficient of variation lower than 45%, preferably
lower than 35%, more preferably lower than 20%. The emulsions suitable in the present
invention are of the type normally employed to obtain halftone, dot and line, images
and are usually called lith emulsions. Lith emulsions contain preferably at least
50 mole % of silver chloride, more preferably at least 80% of silver chloride and
at least about 5% mole of silver bromide. If desired, the silver halide grains can
contain a small amount of silver iodide, in an amount that is usually less than about
5 mole %, preferably less than 1 mole %. Other references to lith materials can be
found in Research Disclosure 235, November 1983, Item 23510, "
Development Nucleation by Hydrazine and Hydrazine derivatives". The silver halide grain average size is lower than about 0.7µm, preferably lower
than about 0.4µm, more preferably lower than 0.2µm. The term "grain size" refers to
the diameter of a circle having the area of the same value as the average area projected
by the silver halide crystals seen at the electron microscope. The silver halide grains
may be those having a regular crystal form, such as a cube or an octahedron, or those
having an irregular crystal form, such as a sphere or tablet, etc., or may be those
having a composite crystal form. They may be composed of a mixture of grains having
different crystal forms.
[0025] The silver halide emulsion may be chemically sensitized with a sulfur sensitizer,
such as allylthiocarbamide, thiourea, cysteine, etc.; an active or inert selenium
sensitizer; a reducing sensitizer such as stannous salt, a polyamine, etc.; a noble
metal sensitizer, such as gold sensitizer, more specifically potassium aurithiocyanate,
potassium chloroaurate, potassium chloroplatinate, etc.; or a sensitizer of a water
soluble salt such as, for instance, of ruthenium, rhodium, iridium, palladium and
the like, more specifically, ammonium chloropalladate, sodium chloropalladite, etc.;
each of such sensitizers being employed either alone or in a suitable combination.
[0026] Further, the silver halide emulsion may be spectrally sensitized by making it, in
addition to its blue light sensitivity, sensitive to, e.g., green light (ortho-sensitive)
or sensitive to green and red light (pan-sensitive). For that purpose the usual monomethine
or polymethine dyes such as acid and basic cyanines, hemicyanines, streptocyanines,
merocyanines, oxonoles, hemioxonoles, styryl dyes or others, as well as trinuclear
or higher nuclear methine dyes, e.g., rhodacyanines or neocyanines can be used. Sensitizers
of this kind have been described, for example, in F.M. Hamer, "
The Cyanine Dyes and Related Compounds", 1964 Interscience Publishers, John Wiley and Sons, New York, and in Research Disclosure
308, December 1989, Item 308119,
Photographic Silver Halide Emulsions, Preparation,
Addenda, Processing and System", Section IV.
[0027] Both chemical and spectral sensitization are not necessarily required and, if practiced,
must not affect the high contrast value.
[0028] The silver halide emulsions can be prepared using a single-jet method, a double-jet
method, or a combination of these methods or can be matured using, for instance, an
ammonia method, a neutralization method, an acid method, etc. At the end of grain
precipitation, water soluble salts are removed from the emulsion with procedures known
in the art, such as ultrafiltration. The emulsions can contain optical brighteners,
antifogging agents and stabilizers, filtering and antihalo dyes, hardeners, coating
aids, plasticizers and lubricants and other auxiliary substances, as those described,
for instance, in Research Disclosure 17643, V, VI, VIII, X, XI and XII, December 1978.
The above described emulsions can be coated onto several support bases by adopting
various methods, as described in Research Disclosure 17643, XV and XVII, December
1978.
[0029] Examples of supports include films of a poly-alpha-olefin (such as polyethylene,
polystyrene, etc.), a polyester (such as polyethyleneterephthalate, etc.), cellulose
esters (such as cellulose triacetate, etc.), paper, synthetic paper or resin-coated
paper and the like.
[0030] The above emulsions may also contain various additives conveniently used depending
upon their purpose. These additives include, for example, stabilizers or antifoggants
such as azaindenes, triazoles, tetrazoles, imidazolium salts, polyhydroxy compounds
and others; film hardeners such as of the aldehyde, aziridine, isoxazole, vinylsulfone,
acryloyl, triazine type, etc.; developing promoters such as benzyl alcohol, polyoxyethylene
type compounds, etc.; image stabilizers such as compounds of the chromane, cumaran,
bisphenol type, etc.; and lubricants such as wax, higher fatty acid glycerides, higher
alcohol esters of higher fatty acids, etc. Also, coating aids, modifiers of the permeability
in the processing liquids, defoaming agents, antistatic agents and matting agents
may be used. References for the kind and for the use of these additives can be found
in Research Disclosure 308, December 1989, Item 308119, "
Photographic Silver Halide Emulsions, Preparation, Addenda, Processing and System".
[0031] The photographic material of the present invention can include a hydrazine derivative
to obtain high contrast images. Any known hydrazine derivatives can be used, such
as, for example, hydrazine derivatives described in Research Disclosure 235, November
1983, Item 23510, "
Development Nucleation by Hydrazine and Hydrazine derivatives".
[0032] In a further aspect the present invention relates to a method for obtaining a half-tone,
dot or line, image, wherein a silver halide photographic material, comprising a support
and coated thereon one or more hydrophilic layers, at least one of said hydrophilic
layers including a high chloride content silver halide emulsion, is image-wise exposed
for forming said image, and subjected to a photographic process comprising an alkaline
developing solution, characterized in that the high-chloride content silver halide
emulsion of said photographic material comprises a polyhydroxybenzene of formula:

wherein n is 1,2 or 3,
and in that the outermost hydrophilic layer of said photographic material comprises
a polydialkylsiloxane preferably having the following formula:

wherein R₁ is an alkyl group having 1 to 3 carbon atoms, R₂ is an alkyl group having
1 to 3 carbon atoms or an alkoxy group having 1 to 2 carbon atoms and n is a positive
integer of from 0 to 2000.
[0033] The present invention does not put any particular restriction on the developing process
of the photosensitive material. In general any developing process can be adopted (comprising
the developing, fixing and etching steps) which is used to process conventional photographic
materials to be used in the lithographic field. Such developing process can be performed
manually or by using automatic processors, at a processing temperature generally ranging
from 18 to 50°C, but also outside said range, if desired.
[0034] The developing solution can contain any known developing agent. Examples of developing
agents (which can be used alone or in mixture) comprise the dihydroxybenzenes (e.g.,
hydroquinone), aminophenoles (e.g., N-methyl-p-aminophenol), 3-pyrazolidones (e.g.,
1-phenyl-3-pyrazolidone), ascorbic acid, and the like. Moreover, such developing solutions
can contain preservatives, alkali agents, buffering agents, antifoggants, water softening
agents, hardeners, and the like. A suitable developing solution which can be used
with the photographic material of the present invention is the so-called lith developing
solution, which comprises a dihydroxybenzene developing agent, an alkali agent, a
small quantity of free sulfite and a buffering agent for the sulfite ions (such as
formaline and sodium bisulfite adducts and acetone and sodium bisulfite adducts) to
monitor the free sulfite concentration, etc.
[0035] The fixing solution can have any conventional composition. Examples of fixing agents
which can be used comprise thiosulfates, thiocyanates and sulfur organic compounds,
known as fixing agents. The fixing solution can further contain water-soluble alluminium
salts as hardeners. The etching solution can have any conventional composition as
well, and, for instance, the compositions described by C.E.K. Mees in "
The Theory of the Photographic Process", McMillan, 1954, pp. 737-744 and precisely an etching solution can be used which
comprises, as a reducing agent, a permanganate, a ferric salt, a persulfate, a cupric
acid, a ceric acid, a hexacyanoferate-(III) or a dichromate, alone or in combination
and, possibly, an inorganic acid such as sulfuric acid, and an alcohol; or an etching
solution can be used which comprises a reducing agent such as a hexacyanoferrate-(III),
ethylenediaminotetracetatoferrate-(III) or the like and a silver halide solvent such
as thiosulfate, thiocyanate, thiourea or a derivative thereof and, possibly, an inorganic
acid such as sulfuric acid. Representative examples of etching solutions are Farmer's
solultions comprising potassium ferrocyanide and sodium thiosulfate, an etching solution
comprising persulfate, an etching solution comprising a ceric salt, etc.
[0036] The present invention is now illustrated with more details by making reference to
the following examples.
EXAMPLE 1
[0037] A cubic monodispersed 0.32 µm silver chlorobromide (40 mole percent bromide) was
prepared as follows. A solution (A) consisting of 4.700 l water, 0.9 g adenine and
84 g of gelatin was initially introduced into a reaction vessel. The components used
for the silver halide grain formation were a solution (B) of 5.379 l water and 2380
g silver nitrate and a solution (C) of 5.281 l water, 688 g KCl, 733 g KBr and 0.002
g Na₃RhCl₆·18H₂O.
Step 1 - Nucleation:
[0038] Solutions (B) and (C) were introduced into the reaction vessel through two separate
inlets simultaneously with a vigorous stirring for a period of 9 minutes with a flow
rate of 51.0 ml/min while the pAg of the content into the vessel was maintained at
8.3 and the volume of the content in the vessel was increased from 4764 ml to 5682
ml and the temperature was maintained at 56°C.
Step 2 - 1st Washing and Concentration:
[0039] Nine minutes after beginning the precipitation, the addition of solutions (B) and
(C) was stopped and the content of the reaction vessel was cycled for 3 minutes through
an ultrafiltration module (fitted with a polysulfone semipermeable membrane, type
PTHK000C5, commercially available from Millipore Co., USA, having a NMWL [Nominal
Molecular Weight Limit] of 100,000) to reduce the content volume in the reaction vessel
from 5682 ml to 2082 ml. The potassium nitrate aqueous sulution formed as a by-product
during the precipitation of silver chlorobromide grains passed through the membrane
was withdrawn, while the filtered silver halide dispersion was returned to the reaction
vessel.
Step 3 - Growth:
[0040] Twelve minutes after beginning, the addition of solutions (B) and (C) into the reaction
vessel was started again for a period of 25 minutes with a flow rate of 72.0 ml/min
and the volume of content in the reaction vessel was increased from 2082 to 5682 ml.
Step 4 - 2nd Washing and Concentration:
[0041] Step 2 was repeated to reduce the content in the reaction vessel from 5682 to 3288
ml.
Step 5 - Growth:
[0042] Forty minutes after beginning, the addition of solutions (B) and (C) to the reaction
vessel started again for a period of 7 minutes with a flow rate of 171 ml/min and
the volume of content in the reaction vessel was increased from 3288 to 5682 ml.
Step 6 - 3rd Washing and Concentration:
[0043] Step 4 was repeated.
Step 7 - Growth:
[0044] Fifty minutes after beginning, step 5 was repeated.
Step 8 - 4th Washing and Concentration:
[0045] Step 4 was repeated.
Step 9 - Growth:
[0046] Sixty five minutes after beginning, step 5 was repeated.
Step 10 - 5th Washing and Concentration:
[0047] After complete additions of solutions (B) and (C), the emulsion was cooled to 40°C
and washed by ultrafiltration until the conductivity was 9,000 micro S.
[0048] Gelatin (1050 g) was added to the content in the reaction vessel while stirring at
45°C until the gelatin was dissolved.
[0049] The resulting emulsion was gold and sulfur sensitized, optically sensitized at 630
nm, divided into six parts and each part added with a polyhydroxybenzene (additive),
as reported in Table 1, and coated onto a polyethylene terephthalate support at a
silver coverage of 4.08 m². A coating composition of aqueous geletin, comprising silicone
as reported in Table 1, was coated onto the emulsion layer as the gelatin protective
layer at a gelatin coverage of 0.70 g/m².
TABLE 1
| Coating |
Additive |
Silicone (*) g/m² |
| |
Type |
M/M Ag |
|
| A |
- |
- |
- |
| B |
- |
- |
0.05 |
| C |
Hydroquinone |
0.05 |
- |
| D |
Hydroquinone |
0.05 |
0.05 |
| E |
Pyrocatecol |
0.05 |
0.05 |
| F |
Resorcinol |
0.05 |
0.05 |
| (*) Polydimethylsiloxane SS 96/100 manufactured by Daw Corning Co. |
[0050] The coatings A-F were subjected to the pressure sensitivity test consisting in applying
a special tungsten carbide stylus with variable weight loading on the surface of unprocessed
film. The coatings were then processed in 3M RDC V lith developer and evaluated by
measuring the minimum weigth necessary to make a visible line. The samples were evaluated
according the following classification:
| Class |
Grams on stylus |
Rating |
| A |
200-170 |
Excellent |
| A-B |
170-140 |
Good |
| B |
140-110 |
Borderline |
| B-C |
110-85 |
Unacceptable |
| C |
85-50 |
" |
| C-D |
50-30 |
" |
| D |
< 30 |
" |
[0051] The results are summarized in the following table 2:
TABLE 2
| Coating |
Pressure Sensitivity Test |
| |
Grams |
Sensitivity |
Class |
| A |
< 25 |
Strong marking |
D |
| B |
90 |
Little marking |
B-C |
| C |
70 |
Little marking |
C |
| D |
190 |
No marking |
A |
| E |
120 |
Very little marking |
B |
| F |
95 |
Little marking |
B-C |
EXAMPLE 2
[0052] A cubic monodispersed silver chlorobromide emulsion was prepared as described in
the previous example 1, chemically and spectrally sensitized, added with hydroquinone
as reported in Table 3 and coated according to Example 1. A gelatin protective layer
comprising silicone was coated onto the emulsion layer as reported in Example 1.
TABLE 3
| Coating |
Additive |
Silicone g/m² |
| |
Type |
M/M Ag |
|
| A |
- |
- |
- |
| B |
- |
- |
0.05 |
| C |
Hydroquinone |
0.05 |
- |
| D |
Hydroquinone |
0.05 |
0.05 |
[0053] The coatings A-D were subjected to the pressure sensitivity test as described in
the previous example 1.
[0054] The results are summarized in the following table 4.
TABLE 4
| Coating |
Pressure Sensitivity Test |
| |
Grams |
Sensitivity |
Class |
| A |
< 25 |
Strong marking |
D |
| B |
100 |
Little marking |
B-C |
| C |
50 |
Marking |
C-D |
| D |
190 |
No marking |
A |
EXAMPLE 3
[0055] A cubic monodispersed silver chlorobromide emulsion was prepared as described in
the previous example 1, chemically and spectrally sensitized, and coated using same
antikinking agents disclosed in literature, such as polymers of US Patent No. 4,485,170,
non-ionic surfactants of JP 62/264,042, and salts of palladium, iridium and tallium
of JP 62/229,129. We have obtained five photographic film according the following
table 5:
TABLE 5
| Coating |
Additive |
g/M Ag |
| A |
Ethylacrylate/Methylmethacrylate 70/30 Copolymer Latex |
130 |
| B |
Superamide™ L9C + Maprofix™ 563 |
80 |
| C |
TlNO₃ |
0.266 |
| D |
K₃lrCl₆ |
0.522 |
| E |
K₂PdCl₄ |
0.326 |
| Superamide™ L9C and Maprofix™ 563 are trade name of the Onyx Chemical Company. Superamide
is the condensation product of diethanolamine and methyl laurate. Maprofix™ 563 is
sodium lauryl sulfate. |
[0056] The coatings A-E were subjected to the pressure sensitivity test as described in
the previous example 1.
[0057] The results are summarized in the following table 6.
TABLE 6
| Coating |
Pressure Sensitivity Test |
| |
Grams |
Sensitivity |
Class |
| A |
< 25 |
Strong Marking |
D |
| B |
< 25 |
Strong Marking |
D |
| C |
< 25 |
Strong Marking |
D |
| D |
< 25 |
Strong Marking |
D |
| E |
< 25 |
Strong Marking |
D |