FIELD OF THE INVENTION
[0001] The present invention relates to a combination of photosensitive elements for use
in radiography. More specifically, the present invention relates to a double-side
coated silver halide radiographic element for use in medical radiography, preferably
for chest diagnostic imaging, and to the combination thereof with a pair of fluorescent
phosphor screens.
BACKGROUND OF THE INVENTION
[0002] It is known in the art of medical radiography to employ intensifying screens to reduce
the X-ray dosage to the patient. Intensifying screens absorb the X-ray radiation and
emit electromagnetic radiations which can be better absorbed by silver halide emulsion
layers. Another approach to reduce the X-ray dosage to the patient is to coat two
silver halide emulsion layers on the opposite sides of a support to form a duplitized
radiographic element.
[0003] Accordingly, it is a common practice in medical radiography to use a radiographic
assembly consisting of a duplitized radiographic element interposed between a pair
of front and back screens.
[0004] One of the problems of medical radiography relates to the different X-ray absorption
of the various parts of the body. For example, in chest radiography the heart area
has an absorption ten times higher than the lung area. A similar effect occurs in
the radiography of the stomach, where a contrast medium is used in order to enhance
the image depictivity (the part of the body having no contrast medium being totally
black), and of hands and legs, where bones have an X-ray absorption higher than that
of soft tissues such as flesh and cartilage.
[0005] In these cases a radiographic element showing a low contrast is required for an area
of high X-ray absorption and a radiographic element showing a high contrast is required
for an area of low X-ray absorption. The resulting film is a compromise in an attempt
to have sufficient optical density and sharpness for these different areas of the
body. In the art of chest radiography, X-ray images providing visually discernible
features in both the heart and lung image areas are attempted by using extended latitude
radiographic elements. Extended latitude radiographic elements typically employ polydispersed
silver halide emulsions to provide lower average contrasts and a wider range of exposures
separating minimum and maximum density exposures. Said extended latitude radiographic
elements, however, do not provide the desired sensitometric curve necessary to obtain
visually useful imaging details in both heart and lung areas. The optimal sensitometric
curve for obtaining good imaging information in both regions of low and high X-ray
absorption is shown in Fig. 1. Various methods have been suggested to solve the problem
of needing different contrast capabilities for different areas of the body. One approach
relates to the use of double coated radiographic elements having a different emulsion
layer coated on each side of the support. An example of this solution can be found
in FR 1,103,973, wherein the use of screens having a light emission ratio of from
1:1 to 1.5:1 (back screen:front screen) in combination with a radiographic element
having coated thereon a high contrast back emulsion and a low contrast front emulsion
is suggested. A combination of screens having a light emission ratio higher than 1.5:1
and radiographic elements having emulsion layers with the same gradation is also suggested.
Other patents disclose the use of double coated radiographic elements having emulsion
layers with different contrast or sensitivity. For example, DE 1,017,464 discloses
a double coated radiographic element having coated thereon a first emulsion with high
sensitivity and low contrast and a second emulsion with low sensitivity and high contrast,
FR 885,707 discloses a double coated radiographic element having coated thereon a
first high speed emulsion and a second high contrast emulsion, and FR 875,269 discloses
a radiographic assembly comprising several radiographic films or papers, each having
a different sensitivity and/or contrast relative to the others, in order to obtain
separate and different images of the same object with a single exposure. Nothing in
the above described patents suggests the use of specific features to obtain a symmetric
double-coated radiographic element showing the sensitometric curve of Fig. 1. An approach
similar to that of the above described French and German patents is disclosed in US
4,994,355, claiming an unsymmetrical double coated radiographic element having emulsion
layers with different contrast, in US 4,997,750, claiming an unsymmetrical double
coated radiographic element having emulsion layers with different sensitivity, and
in US 5,021,327 claiming an unsymmetrical radiographic assembly wherein the back screen
and emulsion layer have a photicity at least twice that of the front screen and emulsion
layer, the photicity being defined as the integrated product of screen emission and
emulsion sensitivity. All these proposed solutions require the use of an unsymmetrical
radiographic film which requires a specific orientation relative to the screens for
a proper use.
[0006] The following are additional documents illustrating the state of the art.
[0007] FR 787,017 discloses a radiographic element comprising silver halide emulsion layers
of different color sensitivity to be combined with intensifying screens emitting radiation
to which the silver halides are sensitive. The purpose of this patent is to obtain
an increased use of radiation.
[0008] EP 88,820 discloses a radiographic fluorescent screen comprising a first blue emitting
phosphor layer and a second green emitting phosphor layer to be combined with a silver
halide element having spectral sensitivity in the blue-green region ("ortho-type"
elements).
[0009] JP 60-175000 discloses a combination of a double coated silver halide element and
a screen pair wherein the fluorescent layers of the two screens have different wavelength
region emissions and each screen comprises an organic dye to absorb the light emitted
by the opposite screen.
[0010] EP 350,883 discloses a technique for crossover reduction in which silver halide emulsion
layers having different color sensitivities are provided on the opposite sides of
a transparent support, and X-ray fluorescent intensifying screens having emission
spectra corresponding to the respective color sensitivities are used.
[0011] Research Disclosure, December 1973, Vol. 116, Item 11620 discloses a radiographic
element which shows different contrast when observed with or without a green filter,
respectively.
[0012] Finally, EP 126,644 describes a radiographic material having a characteristic curve
whose gamma between optical densities of 0.50 and 1.50 is 2.7 to 3.3 and gamma between
optical densities of 2.00 and 3.00 is 1.5 to 2.5, said material having a wide exposure
latitude to make possible the production of images having high diagnostic ability.
SUMMARY OF THE INVENTION
[0013] This invention relates to a double side radiographic element which comprises a support
and at least two silver halide emulsion layers coated on each side of said support,
wherein said at least two silver halide emulsion layers show a speed difference of
at least 0.3 logE and are both sensitive to the same region of the electromagnetic
spectrum, and wherein said double side radiographic element shows a sensitometric
curve having a toe contrast value higher than 0.45 and an average contrast higher
than 1.40.
[0014] In another aspect this invention relates to a symmetrical radiographic assembly comprising:
- a double side radiographic element which comprises a support and hydrophilic colloid
layers coated on each side of said support, and
- an intensifying screen adjacent to each side of said radiographic element,
[0015] wherein on each side of said support are coated at least two silver halide emulsion
layers having a speed difference of at least 0.3 logE, said at least two silver halide
emulsion layers being each sensitive to the same region of the electromagnetic spectrum,
[0016] wherein said intensifying screen comprises a light emitting phosphor selected to
have a radiation light emission having an emission maximum wavelength corresponding
to the region of the electromagnetic spectrum to which said at least two silver halide
emulsion layers are sensitive, and
[0017] wherein said double side radiographic element shows a sensitometric curve having
a toe contrast value higher than 0.45 and an average contrast higher than 1.40.
[0018] In a further aspect, the present invention relates to a process for obtaining a radiographic
image comprising the step of (a) image-wise exposing to an X-ray radiation which has
passed through an object, a symmetrical radiographic assembly comprising (i) a double
side radiographic element having a support and at least two silver halide emulsion
layers having a speed difference of at least 0.3 logE coated on each side thereof,
said at least two silver halide emulsion layers being each sensitive to the same region
of the electromagnetic spectrum, and (ii) an intensifying screen comprising a light
emitting phosphors selected to have a radiation light emission having an emission
maximum wavelength corresponding to the region of the electromagnetic spectrum to
which said at least two silver halide emulsion layers are sensitive, and (b) developing
said exposed radiographic element.
BRIEF DESCRIPTION OF THE DRAWINGS
[0019] Figure 1 represents the optimal sensitometric curve for obtaining good imaging information
in both regions of low and high X-ray absorption, in particular in the chest area
in comparison with a standard sensitometric curve.
DETAILED DESCRIPTION OF THE INVENTION
[0020] This invention relates to a double side radiographic element which comprises a support
and at least two silver halide emulsion layers coated on each side of said support,
wherein said at least two silver halide emulsion layers show a speed difference of
at least 0.3 logE and are both sensitive to the same region of the electromagnetic
spectrum, and wherein said double side radiographic element shows a sensitometric
curve having a toe contrast value higher than 0.45 and an average contrast higher
than 1.40.
[0021] According to the present invention, the double side radiographic element comprises
at least two silver halide emulsions having a difference in speed, measured at density
1.0 above minimum density, of at least 0.3 logE.
[0022] The silver halide emulsion having the higher speed and the silver halide emulsion
having the lower speed will be herein defined as the "high speed emulsion" and the
"low speed emulsion", respectively.
[0023] While the best choice of speed difference between the low speed emulsion and the
high speed emulsion can differ widely, depending upon the application to be served,
in most instances the first and the second emulsion exhibit a speed difference in
the range of from 0.3 to 1.0 logE, optimally from 0.4 to 0.8 logE. It should be understood
that, although in a preferred aspect of the present invention the low speed emulsion
is first coated on the support, and the high speed emulsion is coated on the low speed
emulsion, the order of the coating could be inverted by a man skilled in the art,
without the loss of the benefits of the present invention.
[0024] As known in the photographic art, the contrast is the density difference divided
by the log of the difference in exposure levels at two density reference points on
the characteristic curve, where the exposure levels are meter-candle-seconds. Accordingly,
the contrast y can be measured with the following formula (I):

wherein AD is the density difference and ΔLogE is the difference in speed between
the density reference points. The average contrast is measured at density 0.25 and
2.00 above minimum density. The radiographic film of the present invention provides
an average contrast, measured with the above mentioned formula (I), higher than 1.40,
preferably higher than 1.50.
[0025] On the contrary, the toe contrast value simply represents the speed difference (i.e.,
ALogE) obtained measuring the speed at 0.25 and 1.00 above minimum density. The radiographic
film of the present invention shows a toe contrast value higher than 0.45, preferably
higher than 0.55. In this case, the higher the toe contrast value (which represents
the ΔLogE of the two density reference points), the lower the contrast measured with
the above mentioned formula (I).
[0026] In order to obtain such values of average contrast and toe contrast, the speed difference
of the emulsions coated on the radiographic support should differ of at least 0.3
LogE, preferably of from 0.3 to 1.0 logE, optimally of from 0.4 to 0.8 logE. According
to a preferred embodiment of the present invention the average contrast of the emulsions
coated on the radiographic support should also differ from each other. The contrast
of the high speed emulsion and the low speed emulsion should differ by at least 0.2,
more preferably by at least 0.3. According to a more preferred embodiment of the present
invention the low speed emulsion shows an average contrast in the range of from 2.4
to 3.2, more preferably from 2.6 to 3.0, and the high speed emulsion shows an average
contrast in the range of from 1.8 to 2.6, more preferably from 2.0 to 2.4. Generally,
the best results are obtained when the high and low speed emulsions show the lower
and higher contrast, respectively.
[0027] As employed herein the term "electromagnetic spectrum" refers to radiations having
a wavelength of from 300 to 1200 nm, i.e., comprising the ultraviolet, visible and
infrared radiations.
[0028] The silver halide grains in the radiographic emulsion may be regular grain having
a regular crystal structure such as cubic, octahedral, and tetradecahedral, or a spherical
or irregular crystal structure, or those having crystal defects such as twin planes,
epitaxialisation, or those having a tabular form, or combinations thereof.
[0029] The term "cubic grains" according to the present invention is intended to include
substantially cubic grains, that is, silver halide grains which are regular cubic
grains bounded by crystallographic faces (100), or which may have rounded edges and/or
vertices or small faces (111), or may even be nearly spherical when prepared in the
presence of soluble iodides or strong ripening agents, such as ammonia. The silver
halide grains may be of any required composition for forming a negative silver image,
such as silver chloride, silver bromide, silver chlorobromide, silver bromoiodide,
silver bromochloroiodide, and the like. Particularly good results are obtained with
silver bromoiodide grains, preferably silver bromoiodide grains containing about 0.1
to 15% moles of iodide ions, more preferably about 0.5 to 10% moles of iodide ions
and still preferably silver bromoiodide grains having average grain sizes in the range
from 0.2 to 3 µm, more preferably from 0.4 to 1.5 /1.m. Preparation of silver halide
emulsions comprising cubic silver halide grains is described, for example, in Research
Disclosure, Vol. 176, December 1978, Item 17643, Vol. 184, August 1979, Item 18431
and Vol 308, December 1989, Item 308119.
[0030] Other silver halide emulsions according to this invention having highly desirable
imaging characteristics are those which employ one or more light-sensitive tabular
grain emulsions as disclosed in US Patents 4,425,425 and 4,425,426. The tabular silver
halide grains contained in the silver halide emulsion layers of this invention have
an average diameter to thickness ratio (often referred to in the art as aspect ratio)
of at least 2:1, preferably 3:1 to 20:1, more preferably 3:1 to 10:1, and most preferably
3:1 to 8:1. Average diameters of the tabular silver halide grains suitable for use
in this invention range from about 0.3 µm to about 5 µm, preferably 0.5 µm to 3 µm,
more preferably 0.8 µm to 1.5 µm. The tabular silver halide grains suitable for use
in this invention have a thickness of less than 0.4
/1.m, preferably less than 0.3 µm and more preferably less than 0.2
/1.m.
[0031] The tabular silver halide grain characteristics described above can be readily ascertained
by procedures well known to those skilled in the art. The term "diameter" is defined
as the diameter of a circle having an area equal to the projected area of the grain.
The term "thickness" means the distance between two substantially parallel main planes
constituting the tabular silver halide grains. From the measure of diameter and thickness
of each grain the diameter to thickness ratio of each grain can be calculated, and
the diameter to thickness ratios of all tabular grains can be averaged to obtain their
average diameter to thickness ratio. By this definition the average diameter to thickness
ratio is the average of individual tabular grain diameter to thickness ratios. In
practice, it is simpler to obtain an average diameter and an average thickness of
the tabular grains and to calculate the average diameter to thickness ratio as the
ratio of these two averages. Whatever the method used may be, the average diameter
to thickness ratios obtained do not differ greatly.
[0032] In the silver halide emulsion layer containing tabular silver halide grains, at least
15%, preferably at least 25%, and, more preferably, at least 50% of the silver halide
grains are tabular grains having an average diameter to thickness ratio of not less
than 3:1. Each of the above proportions, "15%", "25%" and "50%" means the proportion
of the total projected area of the tabular grains having an average diameter to thickness
ratio of at least 3:1 and a thickness lower than 0.4
/1.m, as compared to the projected area of all of the silver halide grains in the layer.
[0033] As described above, commonly employed halogen compositions of the silver halide grains
can be used. Typical silver halides include silver chloride, silver bromide, silver
chloroiodide, silver bromoiodide, silver chlorobromoiodide and the like. However,
silver bromide and silver bromoiodide are preferred silver halide compositions for
tabular silver halide grains with silver bromoiodide compositions containing from
0 to 10 mol% silver iodide, preferably from 0.2 to 5 mol% silver iodide, and more
preferably from 0.5 to 1.5 mol% silver iodide. The halogen composition of individual
grains may be homogeneous or heterogeneous.
[0034] Silver halide emulsions containing tabular silver halide grains can be prepared by
various processes known for the preparation of radiographic elements. Silver halide
emulsions can be prepared by the acid process, neutral process or ammonia process,
or in the presence of any other silver halide solvent. In the stage for the preparation,
a soluble silver salt and a halogen salt can be reacted in accordance with the single
jet process, double jet process, reverse mixing process or a combination process by
adjusting the conditions in the grain formation, such as pH, pAg, temperature, form
and scale of the reaction vessel, and the reaction method. A silver halide solvent,
such as ammonia, thioethers, thioureas, etc., may be used, if desired, for controlling
grain size, form of the grains, particle size distribution of the grains, and the
grain- growth rate.
[0035] Preparation of silver halide emulsions containing tabular silver halide grains is
described, for example, in de Cugnac and Chateau, "Evolution of the Morphology of
Silver Bromide Crystals During Physical Ripening", Science and Industries Photographiques,
Vol. 33, No.2 (1962), pp.121-125, in Gutoff, "Nucleation and Growth Rates During the
Precipitation of Silver Halide Photographic Emulsions", Photographic Science and Engineering,
Vol. 14, No. 4 (1970), pp. 248-257,in Berry et al., "Effects of Environment on the
Growth of Silver Bromide Microcrystals", Vol.5, No.6 (1961), pp. 332-336, in US Pat.
Nos. 4,063,951, 4,067,739, 4,184,878, 4,434,226, 4,414,310, 4,386,156, 4,414,306 and
in EP Pat. Appln. No. 263,508.
[0036] In preparing the silver halide emulsions of the present invention, a wide variety
of hydrophilic dispersing agents for the silver halides can be employed. Gelatin is
preferred, although other colloidal materials such as gelatin derivatives, colloidal
albumin, cellulose derivatives or synthetic hydrophilic polymers can be used as known
in the art. Other hydrophilic materials useful known in the art are described, for
example, in Research Disclosure, Vol. 308, Item 308119, Section IX. In a preferred
aspect of the present invention highly deionized gelatin is used. The highly deionized
gelatin is characterized by a higher deionization with respect to the commonly used
photographic gelatins. Preferably, the gelatin for use in the present invention is
almost completely deionized which is defined as meaning that it presents less than
50 ppm (parts per million) of Call ions and is practically free (less than 5 parts
per million) of other ions such as chlorides, phosphates, sulfates and nitrates, compared
with commonly used photographic gelatins having up to 5,000 ppm of Call ions and significant
presence of other ions.
[0037] The highly deionized gelatin can be employed not only in the silver halide emulsion
layers, but also in other component layers of the radiographic element, such as overcoat
layers, interlayers and layers positioned beneath the emulsion layers. In the present
invention, preferably at least 50%, more preferably at least 70% of the total hydrophilic
colloid of the radiographic element comprises highly deionized gelatin. The amount
of gelatin employed in the radiographic element of the present invention is such as
to provide a total silver to gelatin ratio higher than 1 (expressed as grams of Ag/grams
of gelatin). In particular the silver to gelatin ratio of the silver halide emulsion
layers is in the range of from 1 to 1.5.
[0038] The radiographic element of the present invention can be forehardened to provide
a good resistance in rapid processing conducted in automatic processing machine without
the use of hardeners in processing solutions. Examples of gelatin hardeners are aldehyde
hardeners, such as formaldehyde, glutaraldehyde and the like, active halogen hardeners,
such as 2,4-dichloro-6-hydroxy-1,3,5-triazine, 2-chloro-4,6-hydroxy-1,3,5-triazine
and the like, active vinyl hardeners, such as bis-vinylsulfonyl-methane, 1,2-vinylsulfonyl-
ethane, bis-vinylsulfonyl-methyl ether, 1,2-bis-vinylsulfonylethyl ether and the like,
N-methylol hardeners, such as dimethylolurea, methyloldimethyl hydantoin and the like,
and bi-,tri-,or tetra-vinylsulfonyl substituted organic hydroxy compounds, such as
1,3-bis-vinylsulfonyl-2-propanol and the like. Other useful gelatin hardeners may
be found in Research Disclosure, Vol. 308, December 1989, Item 308119, Paragraph X.
[0039] The above described gelatin hardeners may be incorporated in the silver halide emulsion
layer or in a layer of the silver halide radiographic element having a water-permeable
relationship with the silver halide emulsion layer. Preferably, the gelatin hardeners
are incorporated in the silver halide emulsion layer.
[0040] The amount of the above described gelatin hardener that is used in the silver halide
emulsion of the radiographic element of this invention can be widely varied. Generally,
the gelatin hardener is used in amounts of from 0.5% to 10% by weight of hydrophilic
dispersing agent, such as the above described highly deionized gelatin, although a
range of from 1% to 5% by weight of hydrophilic dispersing agent is preferred.
[0041] The gelatin hardeners can be added to the silver halide emulsion layer or other component
layers of the radiographic element utilizing any of the well-known techniques in emulsion
making. For example, they can be dissolved in either water or a water-miscible solvent
such as methanol, ethanol, etc. and added into the coating composition for the above
mentioned silver halide emulsion layer or auxiliary layers.
[0042] The silver halide emulsions can be chemically and optically sensitized by known methods.
[0043] Spectral sensitization can be performed with a variety of spectral sensitizing dyes
known in the art. An example of such spectral sensitizing dyes is the polymethine
dye class, including cyanines, complex cyanines, merocyanines, complex merocyanines,
oxonols, hemioxonols, styryls, merostyryls and streptocyanines.
[0044] Although native UV-blue sensitivity of silver halides is usually known in the art,
significant advantage can be obtained by the use of spectral sensitizing dyes, even
when their principal absorption is in the spectral region to which the silver halide
emulsion have their native sensitivity.
[0045] Preferably, spectral sensitizing dyes according to this invention are those which
exhibit J aggregates if adsorbed on the surface of the silver halide grains and a
sharp absorption band (J-band) with a bathocromic shift with respect to the absorption
maximum of the free dye in aqueous solution. Spectral sensitizing dyes producing J
aggregates are well known in the art, as illustrated by F. M. Hamer, Cyanine Dyes
and Related Compounds, John Wiley and Sons, 1964, Chapter XVII and by T. H. James,
The Theory of the Photographic Process, 4th edition, Macmillan, 1977, Chapter 8. The
use of J-band exhibiting dyes allows the reduction of the well-known problem of crossover.
[0046] In a preferred form, J-band exhibiting dyes are cyanine dyes. Such dyes comprise
two basic heterocyclic nuclei joined by a linkage of methine groups. The heterocyclic
nuclei preferably include fused benzene rings to enhance J aggregation.
[0047] The heterocyclic nuclei are preferably quinolinium, benzoxazolium, benzothiazolium,
benzoselenazolium, benzimidazolium, naphthoxazolium, naphthothiazolium and naphthoselenazolium
quaternary salts.
[0048] J-band type dyes preferably used in the present invention have the following general
formula (I):

wherein
Z1 and Z2 may be the same or different and each represents the elements necessary to complete
a cyclic nucleus derived from basic heterocyclic nitrogen compounds such as oxazoline,
oxazole, benzoxazole, the naphthoxazoles (e.g., naphth{2,1-d}oxazole, naphth-(2,3-d)-oxazole,
and naphth-{1,2-d}-oxazole), thiazoline, thiazole, benzothiazole, the naphthothiazoles
(e.g., naphtho{2,1-d}thiazo!e), the thiazoloquinolines (e.g., thiazolo{4,5-b}quinoline),
selenazoline, selenazole, benzoselenazole, the naphthoselenazoles (e.g., naphtho{1,2-d}selenazole,
3H-indole (e.g., 3,3-dimethyl3H-indole), the benzindoles (e.g., 1,1-dimethylben- zindole),
imidazoline, imidazole, benzimidazole, the naphthimidazoles (e.g., naphth-{2,3-d}-imidazole),
pyridine, and quinoline, which nuclei may be substituted on the ring by one or more
of a wide variety of substitutes such as hydroxy, the halogens (e.g., fluoro, bromo,
chloro, and iodo), alkyl groups or substituted alkyl groups (e.g., methyl, ethyl,
propyl, isopropyl, butyl, octyl, dodecyl, 2-hydroxyethyl, 3-sulfopropyl, carboxymethyl,
2-cyanoethyl, and trifluoromethyl), aryl groups or substituted aryl groups (e.g.,
phenyl, 1-naphthyl, 2-naphthyl, 4-sulfophenyl, 3-carboxyphenyl, and 4-biphenyl), aralkyl
groups (e.g., benzyl and phenethyl), alkoxy groups (e.g., methoxy, ethoxy, and isopropoxy),
aryloxy groups (e.g., phenoxy and 1-naphthoxy), alkylthio groups (e.g., ethylthio
and methylthio), arylthio groups (e.g., phenylthio, p-tolylthio, and 2-naphthylthio),
methylenedioxy, cyano, 2-thienyl, styryl, amino or substituted amino groups (e.g.,
anilino, dimethylanilino, diethylanilino, and morpholino), acyl groups (e.g., acetyl
and benzoyl), and sulfo groups,
R1 and R2 can be the same or different and represent alkyl groups, aryl groups, alkenyl groups,
or aralkyl groups, with or without substitutes, (e.g., carboxymethyl, 2-hydroxyethyl,
3-sulfopropyl, 3-sulfobutyl, 4-sulfobutyl, 2-methoxyethyl, 2-sulfatoethyl, 3-thiosulfatoethyl,
2-phosphonoethyl, chlorophenyl, and bromophenyl),
R3 represents a hydrogen atom,
R4 and R5 can be the same or different and represent a hydrogen atom or a lower alkyl group
of from 1 to 4 carbon atoms,
p and q are 0 or 1, except that both p and q preferably are not 1,
m is 0 or 1 except that when m is 1 both p and q are 0 and at least one of Z, and
Z2 represents imidazoline, oxazoline, thiazoline, or selenazoline,
A is an anionic group,
B is a cationic group, and
k and I may be 0 or 1, depending on whether ionic substitutes are present. Variants
are, of course, possible in which R1 and R3, R2 and Rs, or R1 and R2 together represent the atoms necessary to complete an alkylene bridge.
[0049] Other references to well known spectral sensitizers can be found in Research Disclosure,
Vol. 308, December 1989, Item 308119, Section IV. Research Disclosure is a publication
of Kenneth Mason Publication Ltd., Emsworth, Hampshire P010 7DD, United Kingdom.
[0050] In the most preferred form of this invention, the silver halide emulsions are spectrally
sensitized to the green portion of the electromagnetic spectrum with a spectral sensitizing
dye adsorbed on said silver halide grains represented by the following general formula
(II):

wherein
R10 represents a hydrogen atom or a lower alkyl group of from 1 to 4 carbon atoms (e.g.
methyl, and ethyl),
R6, R7, R8 and Rg each represents a hydrogen atom, a halogen atom (e.g. chloro, bromo, iodo,
and fluoro), a hydroxy group, an alkoxy group (e.g. methoxy and ethoxy), an amino
group (e.g. amino, methylamino, and dimethylamino), an acylamino group (e.g. acetamido
and propionamido), an acyloxy group (e.g. acetoxy group), an alkoxycarbonyl group
(e.g. methoxycarbonyl, ethoxycarbonyl, and butoxycarbonyl), an alkyl group (e.g. methyl,
ethyl, and isopropyl), an alkoxycarbonylamino group (e.g. ethoxycar- bonylamino) or
an aryl group (e.g. phenyl and tolyl), or, together, R6 and R7 and, respectively, R8 and Rg can be the atoms necessary to complete a benzene ring (so that the heterocyclic
nucleus results to be, for example, an a-naphthoxazole nucleus, a b-naphthoxazole
or a b,b'-naphthoxazole),
R11 and R12 each represents an alkyl group (e.g. methyl, propyl, and butyl), a hydroxyalkyl group
(e.g. 2-hydroxyethyl, 3-hydroxypropyl, and 4-hydroxybutyl), an acetoxyalkyl group
(e.g. 2-acetoxyethyl and 4-acetoxybutyl), an alkoxyalkyl group (e.g. 2-methoxyethyl
and 3-methoxypropyl), a carboxyl group containing alkyl group (e.g. carboxymethyl,
2-carboxyethyl, 4-carboxybutyl, and 2-(2-carboxyethoxy)-ethyl), a sulfo group containing
alkyl group (e.g. 2-sulfoethyl, 3-sulfopropyl, 4-sulfobutyl, 2-hydroxy-3-sulfopropyl,
2-(3-sulfopropoxy)-propyl, p-sulfobenzyl, and p-sulfophenethyl), a benzyl group, a
phenetyl group, a vinylmethyl group, and the like,
X- represents an acid anion (e.g. a chloride, bromide, iodide, thiocyanate, methylsulfate,
ethylsulfate, perchlorate, and p-toluensulfonate ion), and
n represents 1 or 2.
[0051] The alkyl groups included in said substitutes R
6, R
7, R
8, Rg, R
io, and R
11 and, more particularly, the alkyl portions of said alkoxy, alkoxycarbonyl, alkoxycarbonylamino,
hydroxyalkyl, acetoxyalkyl groups and of the alkyl groups associated with a carboxy
or sulfo group each preferably contain from 1 to 12, more preferably from 1 to 4 carbon
atoms, the total number of carbon atoms included in said groups preferably being no
more than 20.
[0052] The aryl groups included in said substituents R
6, R
7, R
8 and Rg each preferably contain from 6 to 18, more preferably from 6 to 10 carbon
atoms, the total number of carbon atoms included in said groups arriving up to 20
carbon atoms.
[0053] The following are specific examples of J-band sensitizing dyes belonging to those
represented by the general formula (II) above:

[0054] The silver halide emulsion layers can contain other constituents generally used in
photographic products, such as binders, hardeners, surfactants, speed-increasing agents,
stabilizers, plasticizers, gelatin extenders, optical sensitizers, dyes, ultraviolet
absorbers, etc., and reference to such constituents can be found, for example, in
Research Disclosure, Vol. 176, December 1978, Item 17643, Vol. 184, August 1979, Item
18431 and Vol 308, December 1989, Item 308119.
[0055] The radiographic element of this invention can be prepared by coating the light-sensitive
silver halide emulsion layers and other auxiliary layers on a support. Examples of
materials suitable for the preparation of the support include glass, paper, polyethylene-coated
paper, metals, polymeric film such as cellulose nitrate, cellulose acetate, polystyrene,
polyethylene terephthalate, polyethylene, polypropylene and other well known supports.
Preferably, the silver halide emulsion layers are coated on the support at a total
silver coverage of at least 1 g/m
2, preferably in the range of from 2 to 5 g/m
2.
[0056] Auxiliary layers can be represented by top-coating layers, antistatic layers, antihalo
layer, protective layers, dye underlayers, and the like. Dye underlayers are particularly
useful in order to reduce the crossover of the double coated silver halide radiographic
material of the present invention. Reference to well-known dye underlayer can be found
in US 4,900,652, US 4,855,221, US 4,857,446, 4,803,150. According to a preferred embodiment
of the present invention a dye underlayer is coated on at least one side of the support,
more preferably on both sides of the support, before the coating of said at least
two silver halide emulsions.
[0057] In another aspect this invention relates to a symmetrical radiographic assembly comprising:
- a double side radiographic element which comprises a support and hydrophilic colloid
layers coated on each side of said support, and
- an intensifying screen adjacent to each side of said radiographic element,
wherein on each side of said support are coated at least two silver halide emulsion
layers having a speed difference of at least 0.3 logE, said at least two silver halide
emulsion layers being each sensitive to the same region of the electromagnetic spectrum,
wherein said intensifying screen comprises a light emitting phosphors selected to
have a radiation light emission having an emission maximum wavelength corresponding
to the region of the electromagnetic spectrum to which said at least two silver halide
emulsion layers are sensitive, and
wherein said double side radiographic element shows a sensitometric curve having a
toe contrast value higher than 0.45 and an average contrast higher than 1.40.
[0058] As employed herein the term "symmetrical radiographic assembly" refers to a radiographic
assembly which comprises a silver halide double coated radiographic element comprising
substantially identical silver halide emulsion layers coated on each side of the support,
said radiographic element being interposed between a pair of intensifying screens.
[0059] The radiographic element according to the present invention is associated with the
intensifying screens so as to be exposed to the radiations emitted by said screens.
The pair of screens employed in combination with the radiographic element of the present
invention is symmetrical. The screens are made of relatively thick phosphor layers
which transform the x-rays into light radiation (e. g., visible light). The screens
absorb a portion of x-rays much larger than the radiographic element and are used
to reduce the radiation dose necessary to obtain a useful image.
[0060] The phosphors used in the intensifying screens applied in the present invention have
an emission maximum wavelength in the ultraviolet, blue, green, red or infrared region
of the electromagnetic spectrum according to the region of the electromagnetic spectrum
to which said at least two silver halide emulsion layers are sensitive. More preferably,
said phosphors emit radiations in the ultraviolet, blue and green regions of the electromagnetic
spectrum.
[0061] The green emitting phosphors emit radiation having more than about 80% of its spectral
emission above 480 nm and its maximum of emission in the wavelength range of 530-570
nm. Green emitting phosphors which may be used in the intensifying screens of the
present invention include rare earth activated rare earth oxysulfide phosphors of
at least one rare earth element selected from yttrium, lanthanum, gadolinium and lutetium,
rare earth activated rare earth oxyhalide phosphors of the same rare earth elements,
a phosphor composed of a borate of the above rare earth elements, a phosphor composed
of a phosphate of the above rare earth elements and a phosphor composed of tantalate
of the above rare earth elements. These rare earth green emitting phosphors have been
extensively described in the patent literature, for example in US Patents 4,225,653,
3,418,246, 3,418,247, 3,725,704, 3,617,743, 3,974,389, 3,591,516, 3,607,770, 3,666,676,
3,795,814, 4,405,691, 4,311,487 and 4,387,141. These rare earth phosphors have a high
X-ray absorbing power and high efficiency of light emission when excited with X radiation
and enable radiologists to use substantially lower X radiation dosage levels. Particularly
suitable phosphors for use in the intensifying screens of the present invention are
terbium or terbium-thulium activated rare earth oxysulfide phosphors represented by
the following general formula:

wherein Ln is at least one rare earth element selected from lanthanum, gadolinium
and lutetium, and a and b are numbers such as to meet the conditions 0.0005 < a 0.09
and 0 < b < 0.01, respectively, and terbium or terbium-thulium activated rare earth
oxysulfide phosphors represented by the following general formula:

wherein Ln is at least one rare earth element selected from lanthanum, gadolinium
and lutetium, and a, b and c are numbers such as to meet the conditions 0.0005 ≦ a
< 0.09, 0 < b < 0.01 and 0.65 < c < 0.95, respectively.
[0062] The UV-blue emitting phosphors emit radiation having more than about 80% of their
spectral emission below 450 nm and their maximum of emission in the wavelength range
of 300-400 nm. UV-blue emitting phosphors which may be used in the intensifying screens
of the present invention include UV-blue emitting phosphors known in the art such
as lead or lanthanum activated barium sulfate phosphors, barium fluorohalide phosphors,
lead activated barium silicate phosphors, gadolinium activated yttrium oxide phosphors,
barium fluoride phosphors, alkali metal activated rare earth niobate or tantalate
phosphors etc. UV-blue emitting phosphors are described for example in BE 703,998
and 757,815, in EP 202,875 and by Buchanan et al., J. Applied Physics, vol. 9, 4342-4347,
1968,and by Clapp and Ginther, J. of the Optical Soc. of America, vol. 37, 355-362,1947.
Particularly suitable UV-blue emitting phosphors for use in the intensifying screens
of the present invention are those represented by the following general formula:

wherein x and y are numbers such as to meet the conditions 10-
5 < x 1 1 and 10-
4 < y 0.1 as described in EP 202,875.
[0063] References to other well known kind of light emitting phosphors can be found in Research
Disclosure, Vol. 184, August 1979, Item 18431, Section IX.
[0064] The intensifying screens of this invention have a fluorescent layer comprising a
binder and at least one phosphor dispersed therein. The fluorescent layer is formed
by dispersing the phosphor(s) in the binder to prepare a coating dispersion having
the desired phosphor weight ratio, and then applying the coating dispersion by a conventional
coating method to form a uniform layer. Although the fluorescent layer itself can
be an intensifying screen when the fluorescent layer is self-supporting, the fluorescent
layer is generally provided on a substrate to form an intensifying screen. Further,
a protective layer for physically and chemically protecting the fluorescent layer
is usually provided on the surface of the fluorescent layer. Furthermore, a primer
layer is sometimes provided between the fluorescent layer and the substrate to closely
bond the fluorescent layer to the substrate, and a reflective layer is sometimes provided
between the substrate (or the primer) and the fluorescent layer.
[0065] The binder employed in the fluorescent layer of the intensifying screens of the present
invention, can be, for example, one of the binders commonly used in forming layers:
gum arabic, protein such as gelatin, polysaccharides such as dextran, organic polymer
binders such as polyvinylbutyral, polyvinylacetate, nitrocellulose, ethylcellulose,
vinylidene-chloride-vinylchloride copolymer, polymethylmethacrylate, polybutylmethacrylate,
vinylchloride-vinylacetate copolymer, polyurethane, cellulose acetate butyrate, polyvinyl
alcohol, and the like.
[0066] Generally, the binder is used in an amount of 0.01 to 1 part by weight per one part
by weight of the phosphor. However, from the viewpoint of the sensitivity and the
sharpness of the screen obtained, the amount of the binder should preferably be small.
Accordingly, in consideration of both the sensitivity and the sharpness of the screen
and the easiness of application of the coating dispersion, the binder is preferably
used in an amount of 0.03 to 0.2 parts by weight per one part by weight of the phosphor.
The thickness of the fluorescent layer is generally within the range of 10 µm to 1
mm.
[0067] In the intensifying screens of the present invention, the fluorescent layer is generally
coated on a substrate. As the substrate, various materials such as polymeric material,
glass, wool, cotton, paper, metal, or the like can be used. From the viewpoint of
handling the screen, the substrate should preferably be processed into a sheet or
a roll having flexibility. In this connection, as the substrate is preferably either
a plastic film (such as a cellulose triacetate film, polyester film, polyethylene
terephthalate film, polyamide film, polycarbonate film, or the like), or ordinary
paper or processed paper (such as a photographic paper, baryta paper, resin-coated
paper, pigment-containing paper which contains a pigment such as titanium dioxide,
or the like). The substrate may have a primer layer on one surface thereof (the surface
on which the fluorescent layer is provided) for the purpose of holding the fluorescent
layer tightly. As the material of the primer layer, an ordinary adhesive can be used.
In providing a fluorescent layer on the substrate (or on the primer layer or on the
reflective layer), a coating dispersion comprising the phosphor dispersed in a binder
may be directly applied to the substrate (or to the primer layer or to the reflective
layer).
[0068] Further in the intensifying screens of the present invention, a protective layer
for physically and chemically protecting the fluorescent layer is generally provided
on the surface of the fluorescent layer intended for exposure (on the side opposite
the substrate). When, as mentioned above, the fluorescent layer is self-supporting,
the protective layer may be provided on both surfaces of the fluorescent layer. The
protective layer may be provided on the fluorescent layer by directly applying thereto
a coating dispersion to form the protective layer thereon, or may be provided thereon
by bonding thereto the protective layer formed beforehand. As the material of the
protective layer, a conventional material for a protective layer such a nitrocellulose,
ethylcellulose, cellulose acetate, polyester, polyethyleneterephthalate, and the like
can be used.
[0069] The intensifying screens of the present invention may be colored with a dye. Further,
the fluorescent layer may contain a white powder dispersed therein. By using a dye
or a white powder, an intensifying screen which provides an image of high sharpness
can be obtained.
[0070] In a further aspect, the present invention relates to a process for obtaining a radiographic
image comprising the step of (a) image-wise exposing to an X-ray radiation which has
passed through an object (particularly an animal or human body for medical radiographic
imaging), a symmetrical radiographic assembly comprising (i) a double side radiographic
element having a support and at least two silver halide emulsion layers having a speed
difference of at least 0.3 logE coated on each side thereof, said at least two silver
halide emulsion layers being each sensitive to the same region of the electromagnetic
spectrum, and (ii) an intensifying screen comprising a light emitting phosphors selected
to have a radiation light emission having an emission maximum wavelength corresponding
to the region of the electromagnetic spectrum to which said at least two silver halide
emulsion layers are sensitive, and (b) developing said exposed radiographic element.
[0071] In addition to the features specifically described above, the radiographic elements
of this invention, in the silver halide emulsion layers or in other layers, can include
additional addenda of conventional nature, such as stabilizers, antifoggants, brighteners,
absorbing materials, hardeners, coating aids, plasticizers, lubricants, mating agents,
antikinking agents, antistatic agents, and the like, as described in Research Disclosure,
Vol. 176, December 1978, Item 17643, in Research Disclosure, Vol. 184, August 1979
Item 18431, and in Research Disclosure, Vol. 308, December 1989, Item 308119.
[0072] As regards the processes for the silver halide emulsion preparation and the use of
particular ingredients in the emulsion and in the light-sensitive element, reference
is made to Research Disclosure 184, Item 18431, August 1979, wherein the following
chapters are dealt with in deeper details:
IA. Preparation, purification and concentration methods for silver halide emulsions.
IB. Emulsion types.
IC. Crystal chemical sensitization and doping.
[0073] II. Stabilizers, antifogging and antifolding agents.
IIA. Stabilizers and/or antifoggants.
IIB. Stabilization of emulsions chemically sensitized with gold compounds.
IIC. Stabilization of emulsions containing polyalkylene oxides or plasticizers.
IID. Fog caused by metal contaminants.
IIE. Stabilization of materials comprising agents to increase the covering power.
IIF. Antifoggants for dichroic fog.
IIG. Antifoggants for hardeners and developers comprising hardeners.
IIH. Additions to minimize desensitization due to folding.
III. Antifoggants for emulsions coated on polyester bases.
IIJ. Methods to stabilize emulsions at safety lights.
IIK. Methods to stabilize x-ray materials used for high temperature. Rapid Access,
roller processor transport processing.
[0074]
III. Compounds and antistatic layers.
VI. Protective layers.
V. Direct positive materials.
VI. Materials for processing at room light.
VII. X-ray color materials.
VIII. Phosphors and intensifying screens.
IX. Spectral sensitization.
X. UV-sensitive materials
XII. Bases
[0075] The present invention will be thereafter described by reference to the following
examples which are not intended to be limiting.
EXAMPLE
[0076] An octahedral silver bromochloroiodide emulsion (Em. A) containing 84.4%M bromide,
14.4%M chloride and 1.2%M iodide was sulfur and gold chemically sensitized with gold
thiocyanate complex, sodium p-toluenethiosulfonate,sodium p-toluenesulfinate and benzo-thiazoleiodoethylate,
spectrally sensitized with the green sensitizing dye anhydro-5,5'-dichloro-9-ethyl-3,3'-bis-(3-sulfopropyl)-oxacarbocyanine
hydroxide triethylamine salt, and added with resorcylaldehyde and dimethylol urea
hardeners. The silver halide grains have an average crystal diameter of 0.7µm. When
coated double side on a polyester support emulsion A shows an average contrast of
about 2.8.
[0077] A tabular silver bromoiodide emulsion (Em. B) containing 99.4%M bromide and 0.6%M
iodide was chemically and spectrally sensitized as the above described emulsion A.
The tabular silver halide grains have an average diameter of 1.35µm, an average thickness
of 0.25µm and an aspect ratio of 5.4. When coated double side on a polyester support
emulsion B shows an average contrast of about 2.3.
[0078] Emulsion A and B show a difference in speed of about 0.5 logE.
RADIOGRAPHIC FILM 1 (Invention)
[0079] Emulsion A was coated as first emulsion layer on both sides of a 0,18mm blue polyester
film at a silver coating weight of 1.3 g/m
2 on each side. An emulsion blend was prepared by mixing equal parts (based on silver
content) of emulsion A and B. This emulsion blend was coated over the first emulsion
layer on both sides of the film at a silver coating weight of 1.0 g/m
2. On both emulsion layers was applied a gelatin top coat with a gelatin thickness of
0.9µm.
RADIOGRAPHIC FILM 2 (Invention)
[0080] Emulsion A was coated as first emulsion layer on both sides of a 0,18mm blue polyester
film at a silver coating weight of 1.5 g/m
2 on each side. Emulsion B was coated over the first emulsion layer on both sides of
the film at a silver coating weight of 1.0 g/m
2. On both emulsion layers was applied a gelatin top coat with a gelatin thickness of
0.9µm.
[0081] Both films 1 and 2 were exposed with two 3M Trimax™ T8 screens and also with a combination
of 3M Trimax™ T6 and T16 screens. Trimax™ T6 screen is a medium resolution screen
manufactured by 3M Company, comprising a terbium activated gadolinium oxysulfide phosphor
having an average particle size of 3.5 µm coated in a hydrophobic polymer binder at
a phosphor coverage of 500 g/m
2 and a thickness of 139 µm on a polyester support. Trimax™ T8 screen is a medium resolution
screen manufactured by 3M Company, comprising a green emitting terbium activated gadolinium
oxysulfide phosphor having an average particle size of 8.2 µm coated in a hydrophobic
polymer binder at a phosphor coverage of 420 g/m
2 and a thickness of 105 µm on a polyester support. Trimax™ T16 screen is a high speed
screen manufactured by 3M Company, comprising a terbium activated gadolinium oxysulfide
phosphor having an average particle size of 5.5 µm coated in a hydrophobic polymer
binder at a phosphor coverage of 1050 g/m
2 and a thickness of 250 µm on a polyester support. A 3M XLA™ Radiographic Film and
a Kodak Insight
TM Chest Film were also used as reference. 3M XLA™ Radiographic Film is a conventional
radiographic film having extended latitude, Kodak Insight™ Chest Film is an unsimmetrical
radiographic film having an emulsion layer with high contrast and low speed on one
side and an emulsion layer with low contrast and high speed on the other side.
[0082] The exposed films were processed in a 3M Trimatic
TM XP515 automatic processor at a total processing time of 90 seconds using the developer
and fixer having the following composition.

[0083] The sensitometric results are summarized in the following Tables 1 and 2.

[0084] The data of Tables 1 and 2 clearly show the improvement in terms of toe contrast
value and average contrast of the films 1 and 2 of the present invention, which can
provide a sensitometric curve very similar to the ideal curve of Fig.1.
[0085] It is worth noting that the Kodak Insight™ Film has an unsimmetrical structure, as
described in the above mentioned US 4,994,355, and accordingly, it requires a specific
orientation in order to work well. Moreover, table 1 and 2 clearly show that the Kodak
Insight™ Film also provides different results with different screens in terms of average
contrast and toe contrast value. On the contrary, both Films 1 and 2 maintain the
same sensitometric characteristics even if the screen combination is changed or reversed.
The radiographic film of the present invention does not require a specific care by
the operator having regards the orientation and/or the kind of intensifying screens,
and accordingly can be more easily handled than the prior art chest radiographic films.