FIELD OF THE INVENTION
[0001] The present invention relates to a photographic printing paper support and, more
particularly, to a support which can provide an excellent resolving power when it
is applied to a photographic printing paper, and that at a lower cost than conventionally
used supports.
BACKGROUND OF THE INVENTION
[0002] Hitherto, supports coated with resins on both sides are known as those suitable for
photographic printing paper. In particular, it deserves due notice that the resin
coat provided on the emulsion-coated side (the front resin layer) contains an inorganic
pigment such as titanium oxide, etc., a bluing agent (including blue pigments), a
brightening agent and so on (as described in U.S. Patent 3,501,298) (cf., Fig. 3 illustrated
hereinafter).
[0003] In those supports, it is known that the titanium oxide used therein not only functions
so as to heighten the water resistance and the light reflecting efficiency of the
supports, but also can provide higher resolving power the more its content therein
is increased.
[0004] However, an increase in the content of expensive titanium oxide causes a raise in
the cost of the resulting product. Moreover, the increase of the titanium oxide content
involves a disadvantage of causing an utter lack of production suitability, because
it soils die lips and causes the appearance of fine grains on the resin coat surface,
or the generation of the so-called microglid.
[0005] With the intention of decreasing the titanium oxide content, therefore, it was carried
out to divide the front resin layer into two constituent layers and incorporate titanium
dioxide into the upper constituent layer alone (on the emulsion-coated side, as shown
hereinafter in Fig. 2), as disclosed in JP-B-49-30446 (the term "JP-B" as used herein
means an "examined Japanese patent publication").
[0006] However, the countermeasure described above proved not only to have small effect
upon the improvement of the resolving power, but also to be inadequate for satisfactory
reduction in the cost of the resulting product because it brought about a slight decrease
in the amount of titanium oxide used.
[0007] With the invention of improving the above-described production suitability, on the
other hand, it was carried out to divide the front resin layer into two constituent
layers and design so that not only the titanium oxide content may be higher in the
upper constituent layer than in the lower constituent layer but also the upper constituent
layer may be thinner than the lower constituent layer, as disclosed in JP-A-64-542
(the term "JP-A" as used herein means an "unexamined published Japanese patent application),
or so that not only the titanium oxide content may be lower in the upper constituent
layer than in the lower constituent layer but also the upper constituent layer may
be thinner than the lower constituent layer, as disclosed in JP-A-01-142549.
[0008] However, those methods, although the both introduced an improvement in the production
suitability, didn't made any substantial reduction in the amount of titanium oxide
used. Consequently, they failed in reduction of costs of the resulting products.
[0009] In addition, while it was not a photographic printing paper support, a laminated
sheet was developed for graphic arts (JP-A-03-61038). Such a sheet has two or more
resin layers laminated on the front side of a sheet-form support, and contains titanium
oxide in the topmost resin layer alone. Further, the topmost resin layer thereof is
thinner than the other lower layers.
[0010] Although it is excellent in printability, writing quality and so on, the laminated
sheet described above has a defect that it cannot provide sufficient resolving power
when it is used as photographic printing paper support.
[0011] In order to solve the foregoing problems, the present inventors have made intensive
studies. As a result thereof, it has now been found out that the fuzzy image formation
attributable to a printing operation can be prevented and the content of titanium
oxide can be reduced as the resolving power is kept high to result in reduction of
the product cost when a waterproof resin layer provided on the emulsion-coated side
of a support is constituted of two layers, the upper layer of which contains specified
amounts of titanium oxide and bluing agent and the lower layer of which contains a
bluing agent alone, thereby achieving the present invention.
SUMMARY OF THE INVENTION
[0012] Therefore, an object of the present invention is to provide a photographic printing
paper support which has excellent production suitability and high resolving power
and can be produced at a lower cost than conventional ones.
[0013] The above-described object is attained with a photographic printing paper support
having waterproof resin layers on both sides of a substrate, with the waterproof resin
layer on the emulsion-coated side comprising at least an upper layer containing from
5 to 25 % by weight of titanium oxide and from 0 to 0.56 % by weight of a bluing agent
and a lower layer containing substantially no titanium oxide but containing from 0.05
to 0.60 % by weight of a bluing agent.
BRIEF DESCRIPTION OF DRAWINGS
[0015] Fig. 1 is a cross sectional view showing part of the present support for photographic
printing paper.
[0016] Fig. 2 is a cross sectional view showing part of a conventional support for photographic
printing paper, wherein the waterproof resin layer on the emulsion-coated side is
constituted of two layers and the lower layer of the two does not contain any bluing
agent.
[0017] Fig. 3 is a cross sectional view showing part of another conventional support for
photographic printing paper, wherein the water proof resin layer on the emulsion-coated
side is a single layer.
[0018] In these views, the reference number 1 represents a substrate, the reference numbers
2, 3 and 4 represent waterproof resin layers respectively, the reference number 5
represents a bluing agent, and the reference number 6 represents a titanium oxide.
DETAILED DESCRIPTION OF THE INVENTION
[0019] The waterproof resins used for forming resin layers in the present invention can
be properly chosen from resins of the kind which can undergo melt extrusion at a temperature
ranging from 170 to 290°C. As the resins of such a kind, it is general to use polyolefins,
such as polyethylene, polypropylene, etc., and polyester resins. Of these resins,
polyethylene is preferred over the others. As for the polyethylene, any sort of polyethylene,
a high-density, low-density or linear low-density polyethylene, may be used. Additionally,
these polyethylenes may be used independently or as a mixture of two or more thereof.
[0020] In particular, it is preferable that the waterproof resin used in the foregoing lower
resin layer provided in contact with a substrate on the emulsion-coated side be a
resin having a melt flow rate in the range of 1.2 to 100 g per 10 minutes from the
standpoint of securing satisfactory adhesiveness between the resin layer and the substrate.
Also, it is desirable to use waterproof resins having their melt flow rates in the
range of 1.2 to 100 g per 10 minutes for resin layers other than the lower resin layer
on the emulsion-coated side.
[0021] Additionally, the foregoing lower resin layer may have one or more constituent layers.
[0022] The lowest waterproof resin layer provided on the emulsion-coated side can contain
a tackifier resin and/or an adhesive resin, such as an acid-modified polyolefin resin
capable of hot-sealing waterproof resins, an ionomer, etc., for the purpose of improvement
upon the adhesiveness to both the layer provided thereon and the substrate.
[0023] Suitable examples of such a tackifier resin include resins derived from rosin, terpene
resins (such as β -pinene polymer), cumarone-indene resin, petroleum hydrocarbon resins
and so on.
[0024] A tackifier resin as cited above is generally admixed with the foregoing waterproof
resin in a proportion of from 0.5 to 60 % by weight.
[0025] Specific examples of an adhesive resin as described above include an acid-modified
polyolefin resin, an ionomer, an ethylene-vinyl acetate copolymer resin (EVA resin),
an ethylene-ethylacrylate copolymer resin (EEA resin), an ethylene-acrylic acid copolymer
resin (EAA resin) and a metal salt thereof. The proportion of such an adhesive resin
to the foregoing waterproof resin admixed therewith ranges from 20 to 500 % by weight.
[0026] It is preferable for the upper waterproof resin layer on the emulsion-coated side
to contain a bluing agent in addition to titanium oxide. In the lower waterpoof resin
layer, on the other hand, from 0.05 to 0.60 % by weight of bluing agent is contained,
but titanium oxide is not contained in a substantial sense.
[0027] As for the titanium oxide used in the upper waterproof resin layer, titanium dioxide
is used to advantage because it can ensure higher resolving power to the product.
[0028] It is desirable that the content of titanium oxide in the upper layer be in the range
of 5 to 25 % by weight, particularly preferably 10 to 20 % by weight. When titanium
oxide is used in a content lower than 5 % by weight, the resulting photographic printing
paper cannot achieve sufficiently high resolving power; whereas when the content of
titanium oxide is increased beyond 25 % by weight, not only the production cost of
the support is raised but also the resulting resin layer lacks in production suitability
because it tends to generate cracks and suffer die lines.
[0029] Additionally, the foregoing expression "titanium oxide is not contained in a substantial
sense" means that the content of titanium oxide is not higher than 3 % by weight.
[0030] As for the structure of titanium oxide, both rutile and anatase structures may be
adopted. However, anatase-type titanium oxide is preferred when priority is given
to the achievement of high whiteness; while rutile-type titanium oxide is preferred
when priority is given to the achievement of high sharpness. On the occasion both
whiteness and sharpness are taken into account, on the other hand, a blend of anatase-type
titanium oxide and rutile-type titanium oxide may be used, or the titanium oxide-containing
layer may be subdivided into two layers, namely a layer to which anatase-type titanium
oxide is added and a layer to which rutile-type titanium oxide is added.
[0031] It is desirable that the average grain size of titanium oxide used be in the range
of 0.1 to 0.4 µm. When the titanium oxide has an average grain size less than 0.1
µm, it is difficult to incorporate such titanium oxide in a resin layer in a homogeneously
mixed and dispersed condition; while when the titanium oxide has an average grain
size greater than 0.4 µm, it not only fails to provide sufficient whiteness but also
forms projections at the resin layer surface to exert a bad influence upon image quality.
[0032] Specific examples of titanium oxide having such a structure and an average grain
size as described above include the products commercially available under the trade
names of KA-10 and KA-20 (products of Titan Kogyo Co., Ltd.), and A-220, PF-656, PF-654,
PF-671, PF-715 and CR-63 (products of Ishihara Industry Co., Ltd.).
[0033] In using those titanium oxide products, they are generally subjected to a surface
treatment for the purpose of depressing their activity to inhibit the yellowing phenomenon.
Suitable examples of an agent which can be used for such a surface treatment include
an inorganic material such as hydrated aluminium oxide, hydrated silicon oxide, etc.;
an organic material such as a polyhydric alcohol, a polyamine, a metal soap, an alkyl
titanate, a polysiloxane, etc.; and a mixture of inorganic and organic materials chosen
from those as cited above.
[0034] It is desirable that such a surface treatment agent as cited above be used in a proportion
of from 0.2 to 2.0 % by weight to the titanium oxide when it is an inorganic material,
while when it is an organic material it be used in a proportion of from 0.1 to 1.0
% by weight to the titanium oxide.
[0035] The titanium oxide is kneaded into a waterproof resin with a kneading machine, such
as a two-rod roll, a three-rod roll, a kneader, a Bumbury's mixer or the like. Therein,
a metal salt of higher fatty acid, an ethyl ester of higher fatty acid, a higher fatty
acid amide, a higher fatty acid or so on is further used as dispersing aid. The thus
titanium oxide-incorporated waterproof resin is molded in the form of pellet, and
used as the master batch of titanium oxide.
[0036] It is advantageous that the concentration of titanium oxide in the master batch pellet
ranges generally from about 30 to about 75 %, particularly from 35 to 70 %, by weight
from the standpoints of economy, dispersibility and so on. As for the dispersing aid,
the suitable proportion thereof is generally in the range of about 0.5 to about 10
% by weight to the amount of titanium oxide used. The cases in which the titanium
oxide concentration in the master batch pellet is less than 30 % by weight are too
low in dilution ratio, and so they are bad economy. When the foregoing concentration
is increased beyond 75 % by weight, on the other hand, the dispersibility is lowered
and the resulting resin layer tends to generate cracks by bending.
[0037] Suitable examples of a bluing agent which can be used include generally known pigments,
such as ultramarine, cobalt blue, cobalt phosphate oxide, quinacridone pigments and
mixtures of two or more thereof.
[0038] As for the bluing agent used in the present invention, it is preferable from the
standpoint of improving the resolving power that the grain size thereof be in the
range of 0.05 to 5 µm, particularly 0.1 to 3 µm.
[0039] In using a bluing agent for the upper layer of the present waterproof resin layers,
its content therein is desirably chosen from the range of 0 to 0.56 % by weight, preferably
0.05 to 0.4 % by weight, and particularly preferably 0.07 to 0.30 % by weight. Although
sharpness is improved by increasing the content beyond 0.56 % by weight, a bluish
tinge is given to the image thereby to diminish the value of the resulting material
as goods.
[0040] When the bluing agent is used in the lower layer of the present waterproof resin
layers, it is desirable that its content therein range from 0.05 to 0.60 % by weight,
preferably from 0.07 to 0.45 % by weight, and particularly preferably from 0.10 to
0.30 % by weight. When the content is below 0.05 % by weight, low-frequency CTF values
are lowered, and thereby is lessened the resolution heightening effect.
[0041] The bluing agent is kneaded into a waterproof resin with a kneading machine, such
as a two-rod roll, a three-rod roll, a kneader, a Bumbury's mixer or the like. The
bluing agent-incorporated waterproof resin thus obtained is molded in the form of
pellet, and used as the master batch of bluing agent.
[0042] From the standpoints of economy, dispersibility and so on, it is desirable that the
concentration of a bluing agent in the master batch pellet range from about 1 to about
30 %. In forming the master batch pellet, the titanium oxide can be kneaded together,
if needed, and a dispersing aid such as a metal salt of higher fatty acid, an ethyl
ester of higher fatty acid, a higher fatty acid amide, a higher fatty acid, etc. can
be used for assisting the homogeneous dispersion of the bluing agent.
[0043] In addition, the waterproof resin layers according to the present invention can contain
an antioxidant. As for the proportion of an antioxidant to the waterproof resin, the
order of 50-1,000 ppm is desirable from the standpoint of inhibiting the resin from
deteriorating without accompanied by adverse effects on photographic properties.
[0044] The thus prepared master batch pellets, in which the titanium oxide and/or the bluing
agent is incorporated, are properly diluted with a waterproof resin, and used for
coating purpose.
[0045] Specifically, the foregoing pellets containing the titanium oxide and/or the bluing
agent together with the waterproof resin required for dilution are fused by heating,
and then spread over a traveling substrate made of natural pulp paper, synthetic paper
or the like in the form of melt films according to a successive lamination method
or a lamination method using a co-extruding die of feed block type, multi-manifold
type, multi-slot type or so on. Thus, the waterproof resin layers constituting the
present support can be formed.
[0046] Although the present invention has no particular restriction as to the shape of the
die used for co-extrusion, it is generally preferred to use a T-die or a coat hanger
die.
[0047] As for the waterproof resin layers provided on the front side of the support, it
is preferable to firstly form the resin layer containing a bluing agent on the front
side of the support (on the emulsion-coated side) and then form the titanium oxide-containing
waterproof resin layer as a laminate film on the foregoing resin layer by the melt
extrusion from a slit die under a temperature ranging from 170 to 290°C.
[0048] When the melt extrusion temperature is below 170 °C , the waterproof resin cannot
undergo sufficient oxidation to result in the lowering of adhesiveness between the
waterproof resin layer and the substrate; while when it is above 290 °C the resin
layer surface comes to have cracks and die lines, which considerably mar the appearance.
[0049] Before it is covered with the resin, the substrate is preferably subjected to an
activating treatment, such as a corona discharge treatment, a flame treatment, a glow
discharge treatment, a plasma treatment or so on.
[0050] As for the present waterproof resin layer which is basically constituted of two layers,
it is desirable that the thickness of the upper layer be in the range of 5 to 35 µm,
preferably 10 to 25 µm and particularly preferably 15 to 25 µm, and the thickness
of the lower layer be in the range of 5 to 30 µm, preferably 10 to 25 µm and particularly
preferably 15 to 20 µm.
[0051] The topmost surface of the waterproof resin layer on the emulsion-coated side is
subjected to a die embossing treatment of the type which can put thereon a gloss or
the fine grain described in JP-A-55-26507 or can render the surface mat or silk. On
the other hand, the waterproof resin layer on the back side is subjected to another
type of die embossing treatment by which the surface is made dull.
[0052] The surfaces having received such a die embossing treatment as described above can
be subjected to an activating treatment such as a corona discharge treatment, a flame
treatment, etc., and further can undergo the subbing treatment as described in JP-A-61-846443.
[0053] The substrate used in the present invention may be any kind of paper. Specifically,
paper in general which contains natural pulp as a main component, paper made of a
natural pulp-synthetic fiber mixture, synthetic fiber paper containing synthetic fibers
as a main component, the so-called synthetic paper which can be obtained, e.g., by
processing a synthetic resin film, such as a polystyrene film, a polypropylene film,
etc., so as to closely resemble to paper in appearance, and so on can be used as the
substrate. However, it is particularly favored to use natural pulp paper (which is
conventionally called "a raw paper" hereinafter) as the substrate of photographic
printing paper.
[0054] Specific examples of chemicals which can be added to a raw paper include alkylketene
dimers, fillers such as clay, talc, calcium carbonate, fine particles of urea resin,
etc., a sizing agent such as rosin, higher fatty acid salts, paraffin waxes, alkenylsuccinic
acids, etc., a paper strengthening agent such as polyacrylamides, etc., and a fixing
agent such as sulfate band, etc. Further, dyes, fluorescent dyes, slime controlling
agent, an anti-foaming agent and so on can be added to a raw paper, if needed.
[0055] Furthermore, a softening agent can be added, if desired. As for the softening agent,
it can be referred to, e.g.,
Shin-Kamikako Binran (which means "New Handbook of Paper Finishing"), pp. 554-555, Shiyaku Times Co. (1980).
Of the softening agents cited therein, those having a molecular weight of at least
200 are preferred in particular. Such softening agents have a hydrophobic group containing
at least 10 carbon atoms and take the form of amine or quaternary ammonium salt which
enables self-fixation to cellulose.
[0056] Specific examples of such a softening agent include the reaction products of maleic
anhydride copolymers with polyalkylenepolyamines, the reaction products of higher
fatty acids with polyalkylenepolyamides, the reaction products of urethane alcohols
with alkylating agents, and the quaternary ammonium salts of higher fatty acids. In
particular, the reaction products of maleic anhydride copolymers with polyalkylenepolyamines
and the reaction products of urethane alcohols with alkylating agents are preferred
over the others.
[0057] On the other hand, a raw paper can also undergo a surface-size treatment with a film-forming
polymer, such as gelatin, starch, carboxymethyl cellulose, polyacrylamide, polyvinyl
alcohol, modified polyvinyl alcohols, etc. As for the modified polyvinyl alcohols,
the polyvinyl alcohols modified with carboxyl groups, those modified with silanols
and the copolymers with acrylamides are examples thereof. The coverage of such a film-forming
polymer is controlled to from 0.1 to 5.0 g/m², preferably from 0.5 to 2.0 g/m².
[0058] To the film-forming polymer can further be added an antistatic agent, a brightening
agent, a pigment, an anti-foaming agent and so on, if needed.
[0059] A pulp slurry which contains pulp and optional additives as described above, including
a filler, a sizing agent, a paper strengthening agent, a fixing agent and so on, is
made into paper by means of a paper machine such as a Fourdrinier machine, dried and
then rolled up to prepare a raw paper. Before or after the drying operation, the paper
can be subjected to a surface-size treatment as described above. In addition, the
paper undergoes a calendering treatment in a period between the drying and rolling-up
operations.
[0060] In the case where the paper undergoes a surface-size treatment after the drying operation,
the calendering treatment can be carried out either before or after the surface-size
treatment. However, it is desirable that the calendering treatment be carried out
after other intended treatments, or at the final stage of finishing. In the calendering
treatment described above, there can be used conventional metal rolls and spring rolls
used for papermaking.
[0061] The raw paper used for the present photographic printing paper support is prepared
so as to finally attain a thickness of from 50 to 250 µm by the calendering treatment
as described above. The density of the raw paper ranges from 0.8 to 1.3 g/m³, preferably
from 1.0 to 1.2 g/m³.
[0062] The photographic printing paper support according to the present invention can be
coated with various backing layers for the purposes of prevention of charging, curling
or other phenomena. In such backing layers can be contained properly chosen and combined
additives. Such additives include the inorganic and organic antistatic agents, the
hydrophilic binders, the latexes, the hardeners, the pigments and the surfactants
disclosed or recited in JP-B-52-18020, JP-B-57-9059, JP-B-57-53940, JP-B-58-56859,
JP-A-59-214849 and JP-A-58-184144.
[0063] The photographic printing paper support according to the present invention is coated
with various photographic constituent layers, and serves for the various purposes,
as color photographic printing paper, black-and-white photographic printing paper,
printing paper for photocomposition, reversal photographic materials, negative and
positive materials for silver salt diffusion transfer process, graphic arts materials
and so on For instance, those photographic constituent layers can include an emulsion
layer comprising silver chloride, silver bromide, silver chlorobromide, silver iodobromide
or silver chloroiodobromide, color coupler-incorporated silver halide emulsion layers
for a multilayer color photographic material, or a silver salt diffusion transfer
image-receiving layer in which physical development nuclei are incorporated.
[0064] In accordance with the present invention, the titanium oxide content in a photographic
printing paper support can be reduced. As a result of it, the present support not
only can have excellent production suitability but also can be produced at a lower
price than conventional ones When the present support is used as a support of photographic
printing paper, the resulting photographic printing paper can be prevented from suffering
the fuzzy image formation attributable to a printing operation. Therefore, the present
support has a great advantage in that it can ensure high resolving power to photographic
printing paper.
[0065] The present invention will now be illustrated in more detail by reference to the
following examples. However, the invention should not be construed as being limited
to these examples.
EXAMPLE 1
[0066] A paper substrate 1 (See Fig. 1) having a basis weight of 170 g/m² was surface-treated
by corona discharge having an output of 1 KW, and a low density polyethylene resin
(density: 0.94 g/cm³, a melt index: 3.0) was extrusion-laminated on the back side
thereof at a line speed of 200 m/min under a temperature of 260°C to form a waterproof
resin layer 4 having a thickness of 40 µm.
[0067] Then, a bluing agent-containing waterproof resin layer 2 (lower layer) and a titanium
oxide-containing waterproof resin layer 3 (upper layer), whose compositions and the
thicknesses are set forth in Table 1, were coextrusion-laminated on the front side
(or the emulsion-coated side) of the paper substrate 1 under the same condition as
described above to prepare a photographic printing paper support according to the
present invention (See Fig. 1).
Table 1
Layer No. |
Ingredient |
Proportion (wt%) |
Thickness |
3 (upper) |
Low-density polyethylene (density: 0.918 g/cm³) |
80.0 |
20 µm |
Anatase-type titanium oxide (surface coating: treatment with 0.4 % Al₂O₃) |
20.0 |
Ultramarine |
0 |
2 (lower) |
Low-density polyethylene (density: 0.918 g/cm³) |
99.93 |
20 µm |
Ultramarine |
0.07 |
[0068] The thus obtained support was coated with color emulsions to provide a photographic
printing paper. Then, the photographic printing paper was subjected to printing and
developing operations, thereby obtaining a photograph.
[0069] The photograph obtained was examined for resolving power by visual observation. In
evaluating the resolving power, the observation result was classified into 10 grades,
and the grade 5 as a standard was given to the resolving power of a conventional case
(Comparative Example 5 described hereinafter), wherein a single waterproof resin layer
was provided. The evaluation result is shown in Table 2.
EXAMPLE 2 AND COMPARATIVE EXAMPLES 1 TO 5
[0070] Photographic printing paper supports were prepared in the same manner as in Example
1, except that the compositions of the upper and the lower waterproof resin layers
were changed to those set forth in Table 2 respectively. Additionally, the waterproof
resin layer in Comparative Example 5 was not divided into two layer, but it was formed
into a single layer having a thickness of 40 µm. The same color emulsions as used
in Example 1 were coated on each of these supports to produce photographic printing
papers. The thus produced printing papers were each subjected to the same printing
and developing operations as in Example 1, and examined for resolving power by the
same method as in Example 1. The results obtained are shown in Table 2.
Table 2
|
Layer No. |
Composition |
Resolving Power |
Low-density Polylethylene (wt%) |
Titanium Dioxide (wt%) |
Bluing Agent (wt%) |
|
Example 1 |
3 |
80.0 |
20.0 |
0 |
8 |
2 |
99.93 |
0 |
0.07 |
Example 2 |
3 |
89 |
11 |
0 |
7 |
2 |
99.93 |
0 |
0.07 |
Comparative Example 1 |
3 |
79.93 |
20 |
0.07 |
7 |
2 |
100 |
0 |
0 |
Comparative Example 2 |
3 |
79.93 |
20 |
0.07 |
8 |
2 |
94 |
6 |
0 |
Comparative Example 3 |
3 |
88.93 |
11 |
0.07 |
5 |
2 |
100 |
0 |
0 |
Comparative Example 4 |
3 |
88.93 |
11 |
0.07 |
7 |
2 |
91 |
9 |
0 |
Comparative Example 5 |
single layer |
89.965 |
10 |
0.035 |
5 |
[0071] Making a comparison between the samples having the same titanium oxide content, it
is proved by the above table that the support containing a bluing agent in tile upper
layer alone is inferior in resolving power to the support containing it in the lower
layer alone. In particular, the distinction in resolving power is remarkable between
the samples which are reduced in titanium oxide content (as can be seen in the comparison
between Comparative Example 3 and Example 2). As a reason why such a distinction is
brought about, it can be thought that the support containing no bluing agent in the
lower layer suffers diffused reflection of light by the substrate surface.
EXAMPLES 3 TO 4 AND COMPARATIVE EXAMPLE 6
[0072] Photographic printing paper supports were prepared in the same manner as in Example
1, except that the content of the bluing agent in the lower layer 2 was changed to
0.28 wt% (Example 3), 0.56 wt% (Example 4) and 0.84 wt% (Comparative Example 6), respectively.
The same color emulsions as used in Example 1 were coated on each of these supports
to produce photographic printing papers. The thus produced printing papers were each
subjected to the same printing and developing operations as in Example 1, and examined
for resolving power by the same method as in Example 1.
[0073] The examination results showed that the resolving power was heightened with an increase
in bluing agent content. However, the photograph came to assume a stronger tinge of
blue the higher the bluing agent content became, and so the sample having the bluing
agent content of 0.84 wt% was undesirable from the practical viewpoint of image quality.