BACKGROUND OF THE INVENTION
Field of the invention
[0001] This invention relates to a recording medium for a printer containing an interlayer
compound for fixing and holding a water-soluble dye by an intercalation reaction which
is based on the ion exchange action.
Description of the Related Art
[0002] Among systems for outputting on a recording medium the image information or the letter
code information prepared by a personal computer or a word processor, there is an
ink jet recording system of emitting an aqueous ink containing a water-soluble dye
onto a recording medium for a printer for forming an image from a recording nozzle
having an electrical field, heat or the pressure as a driving source.
[0003] This ink jet recording system recently has come into widespread use in offices or
home because it is only low in noise during recording and in running cost is low and
an image can be formed on an ordinary paper sheet while wastes such as used ink ribbons
are not produced.
[0004] Meanwhile, the dye used in general in this ink jet recording system is held on the
dye fixing layer, after it is transferred to the dye fixing layer, by the force of
interaction with constituent components of the dye fixing layer, such as the Van del
Waals force or hydrogen linkage. Thus, if the solvent, such as water, having stronger
affinity to these dyes, is contacted with the image after image formation, the dye
tends to be dissolved from the dye fixing layer to the solvent thus causing image
blurring. If the heat energy or the water vapor sufficient to counteract the Van del
Waals force or the hydrogen linkage between the water-soluble dye making up the image
and the constituent elements of the dye fixing layer is supplied to the recording
medium for the printer, the water-soluble dye tends to be moved to cause the image
blurring. Moreover, if the water-soluble dye making up the image is exposed to light
rays of a higher energy, such as ultraviolet light, the image tends to be faded or
changed in color tone or or lowered in concentration due to decomposition of the dye
itself.
[0005] For improving image fixation, such as water-proofness, in this ink jet recording
system, it has been proposed to fix and hold the dye on the dye fixing layer by an
intercalation reaction which is based on the ion exchange action. There is proposed
in Japanese Laying-Open patent Application 7-69725 a dye fixing layer in which an
interlayer compound having an ion exchange function is used as a mixture with hydrophilic
binder resins, such as a polyvinyl pyrrolidone resin, a polyvinyl butyral resin, hydroxy
propyl cellulose resin or polyvinyl alcohol resin.
[0006] Also, a proposal has been made of treating the interlayer compound with an organic
acid for improving the ink fixation.
[0007] Moreover, attempts have been made for modifying the molecular structure of the dye
for improving the light-fastness of the image.
[0008] However, the above-described systems are insufficient in effectuating dye fixation
to the interlayer compound, such that the image perservability, especially light-fastness,
remains insufficient, thus presenting difficulties in realising the fixation comparable
to that realized with a silver halide photo.
[0009] Thus, difficulties are feared to be met in using an image formed on a recording medium
by the conventional ink jet recording system in the fields of application in which
high image durability is required, such as a certification photo or printed matter
for outdoor display. However, even in these fields of application, it has been a desideratum
to improve the image durability for realizing image formation by the ink jet recording
system.
SUMMARY OF THE INVENTION
[0010] It is therefore an object of the present invention to overcome the above-mentioned
problems of the prior art and to provide a recording medium for a print er containing
an interlayer compound for fixing and holding a water-soluble dye by an intercalation
reaction which is based on the ion exchange action, in which the recording medium
has superior ink fixation and water-proofness and in which an image formed thereon
has improved light-fastness.
[0011] For accomplishing the above object, the preset inventors have conducted perseverant
researches and have found that, if an organic acid is newly added besides the organic
acid used for improving the fixation between the interlayer compound and the aqueous
ink, the image formed on the recording medium for the printer can be improved significantly
in light-fastness.
[0012] The preset invention provides a recording medium for a printer containing an interlayer
compound used for fixing and holding a water-soluble dye by an intercalation reaction
which is based on the ion exchange action, wherein at least one organic acid is contained
in an amount of 5 to 100 wt% related to the interlayer compound.
[0013] If the organic acid is contained in an amount of 5 to 100 wt%, related to the interlayer
compound, not only the ink fixation properties and water-proofness can be improved
in forming an image on a recording medium, but also the light-fastness of an image
can be improved.
[0014] If the content of the organic acid is less than 5 wt%, the image is lowered in water-proofness
and light-fastness. If the content of the organic acid exceeds 100 wt%, the proportion
of the resin is correspondingly decreased, thus lowering adhesion and water-proofness
to lead to lowered ink permeation and loss of luster as the recording medium thus
detracting from the image quality.
[0015] The organic acid 5 preferably has 1 to 20 carbon atoms.
[0016] Preferably, the recording medium for a printer is made up at least of a substrate
and a dye fixation layer formed of a binder resin and which is formed on a substrate.
The interlayer compound is contained in the dye fixation layer in an amount of 10
to 90 wt% related to the solid content in the dye fixation layer.
[0017] If the content of the interlayer compound is less than 10 wt%, the dye fixing effect
is lowered, whereas, if the content of the interlayer compound exceeds 90 wt%, the
resin content in the solid content making up the dye fixation layer is relatively
decreased to lower the flexibility.
[0018] As this interlayer compound, a layered inorganic high molecular material, formed
of a mineral of the hydrotalcite group, is preferably employed.
[0019] Also preferably, the recording medium for a printer is made up of a substrate, a
dye fixation layer formed of a binder resin and an ink absorbing layer formed of an
ink-absorbing resin. The ink-absorbing resin is formed on the dye fixation layer,
while the dye fixation layer is formed on the substrate. An organic acid is contained
in the ink absorbing layer in an amount of 10 to 150 wt% related to the weight of
the ink-absorbing resin.
[0020] If the content of the organic acid is less than 10 wt%, the image is lowered in water-proofness
and light-fastness. If the content of the organic acid exceeds 150 wt%, the amount
of the resin is correspondingly decreased, thus lowering adhesion and water-proofness
to lead to lowered ink permeation and loss of luster as the recording medium thus
detracting from the image quality.
[0021] In the structure of the recording medium for the printer, it may be a double-layered
structure comprised of a substrate and a dye fixation layer of a binder resin formed
thereon, or a three-layered structure additionally including an ink absorbing layer
of an ink-absorbing resin formed on the dye fixation layer.
[0022] It suffices if the interlayer compound is contained in the dye fixation layer while
the organic acid is contained in at least one of the dye fixation layer and the ink
absorbing layer.
[0023] It is seen from above that, since a pre-set amount of the organic acid is contained
in the recording medium for a printer according to the present invention, not only
the ink fixation properties and water-proofness can be improved when forming an image
on the recording medium, but also the image formed on the recording medium can be
improved significantly in light-fastness.
[0024] That is, the recording medium for a printer according to the present invention has
durability comparable to a silver halide photo, such that it can be satisfactorily
used as a certification photo or as printed matter for outdoor display purposes.
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] Fig.1 is a schematic view showing a structure of a recording medium for a printer
embodying the present invention.
[0026] Fig.2 is a schematic view showing another structure of a recording medium for a printer
embodying the present invention.
[0027] Fig.3 is a schematic view showing still another structure of a recording medium for
a printer embodying the present invention.
[0028] Fig.4 is a schematic view showing yet another structure of a recording medium for
a printer embodying the present invention.
DESCRIPTION OF PREFERRED EMBODIMENTS
[0029] Referring to the drawings, preferred embodiments of recording medium for a printer
according to the present invention will be explained in detail.
[0030] The recording medium for a printer, according to the present invention, contains
an interlayer compound for fixing and holding the water-soluble dye by an intercalation
reaction based on the ion exchange action and also contains at least one organic acid
in an amount of 5 to 100 wt% related to the weight of the interlayer compound.
[0031] The organic acid, thus added to the recording medium for a printer, improves the
fixation between the interlayer compound and the aqueous ink. Moreover, if added in
a pre-set amount to an ink absorbing layer and a dye fixation layer, the organic acid
accords superior ink filtration characteristics and water-proofness, while improving
the light-fastness of the image formed on the recording medium for the printer.
[0032] If the amount of the organic acid is less than 5 wt%, the image is lowered in water-proofness
and light-fastness. If the amount of the organic acid exceeds 100 wt%, adhesion to
a substrate and to other layers is lowered to deteriorate water-proofness, while the
permeation characteristics of the aqueous ink is lowered and the recording medium
becomes delustered to detract from the picture quality.
[0033] The recording medium for the printer according to the present invention is composed
at least of a substrate and a dye fixation layer of a binder resin formed on the substrate.
That is, the recording medium for the printer may be of a double layer structure composed
of a substrate and the dye fixation layer formed of the binder resin and which is
formed on the substrate. Alternatively, the recording medium for the printer may be
of a three-layered structure further including an ink absorption layer on the dye
fixation layer.
[0034] In the latter case, the interlayer compound is contained in the dye fixation layer,
whilst the organic layer is contained in at least one of the dye fixation layer and
the ink absorption layer.
[0035] Specifically, a first embodiment of the recording medium for a printer is of a double-layer
structure, made up of a substrate 1 and a dye fixation layer 2, formed in this order,
as shown in Fig.1. An interlayer compound 4 and at least one organic acid 5 are contained
in the dye fixation layer 2.
[0036] A second embodiment of the recording medium for a printer is of a three-layer structure
composed of a substrate 1, a dye fixation layer 2 and an ink absorbing layer 3, formed
in this order, and an interlayer compound 4 and at least one organic acid 5 are contained
in the dye fixation layer 2, as shown in Fig.2. The ink absorbing layer 3 absorbs
water or alcohols, used as solvents for the aqueous ink used, to improve permeation
characteristics of the aqueous ink.
[0037] Similarly to the second embodiment, a third embodiment of the recording medium for
a printer is of a three-layer structure and contains the interlayer compound 4 in
the dye fixation layer 2, while containing at least one organic acid 5 in the ink
absorbing layer 3.
[0038] Similarly to the second embodiment, a fourth embodiment of the recording medium for
a printer is of a three-layer structure, and contains an interlayer compound 4 and
at least one organic acid 5 in the dye fixation layer 2, while containing at least
one organic acid 5 in the ink absorbing layer 3.
[0039] In any of the above-described embodiments of the recording medium for a printer,
the desired meritorious effect may be achieved. The ink absorbing layer 3, however,
is preferably provided for improving ink absorption properties.
[0040] The recording medium for the printer according to the present invention is characterized
in that 5 to 100 wt% of the organic acid 5 is contained in the interlayer compound
4. If, however, the organic acid 5 is contained in the ink absorbing layer 3, as in
the third and fourth embodiments, it is more preferred that the amount of the organic
acid 5 in the ink absorbing layer 3 be 10 to 150 wt% based on the weight of the ink
absorbing resin.
[0041] If the amount of the organic acid 5 is less than 10 wt%, the image is lowered in
water-proofness and light-fastness. If the amount of the organic acid 5 exceeds 150
wt%, the proportion of the resin is proportionately lowered, thus leading to the lowering
of adhesion, water-proofness and ink infiltration and to a loss of luster as a recording
medium to detract from the image quality.
[0042] The organic acids may be enumerated by carboxylic acid, sulfonic acid, sulfinic acids,
enol, imide, oxime and aromatic sulfonamide. The number of these organic acids is
preferably 1 to 20. These organic acids may be used alone or in combination.
[0043] The dye fixation layer preferably contains the interlayer compound in an amount of
10 to 90 wt% related to the solid content in the dye fixation layer.
[0044] If the amount of the interlayer compound is less than 5 wt%, the dye fixation effect
is lowered. Conversely, if the amount of the interlayer compound exceeds 90 wt%, the
content of the resin in the solid content making up the dye fixation layer is relatively
lowered to deteriorate the flexibility.
[0045] For this interlayer compound, it is preferred to use a layered inorganic high molecular
material having excellent water absorption or water swelling properties and exhibiting
an anion exchange capability. For example, a mineral of the hydrotalcite group having
exchange anions is preferably employed. In particular, natural minerals of the hydrotalcite
group having the composition of Mg
0.7Al
0.3O
1.15 is preferred. Alternatively, synthesized products having a slightly different composition
may also be used.
[0046] Like natural products, fine powders of the synthesized product are free of foreign
matter, and present a pure white color, with crystals per se being optically transparent.
Thus, if the fine powders of the synthesized product are contained in the dye fixation
layer as the interlayer compound, an image can be formed which has a color saturation
comparable to that of silver halide photos. Alternatively, such a mineral corresponding
to the mineral of the hydrotalcite group having, in its ion exchange site, inorganic
ions, such as NO
3-, SO
42-, CLO
4-, Fe(CN)
6-4, ions of heteropolyphosphric acid, or lower carboxylate ions having hydrophilic organic
anions, capable of undergoing solvation with a high dielectric constant medium, such
as water or alcohol, may be used. In contradistinction from the above ions, higher
carboxylate ions tend to give an interlayer which hardly undergoes solvation and hence
are not desirable.
[0047] For improving dispersibility to binder resins as later explained or improving swelling
properties with respect to non-aqueous solvents, such as alcohols, such an interlayer
compound having a portion of exchange anions replaced by organic anions for widening
the interlayer separation (pillar effect) or partially hyrophobilizing the interlayer
may be used. Preferred organic anions may be enumerated by carboxylic acid anions,
sulfonic acid anions, ester anions or phosphoric acid ester anions.
[0048] The dye fixation layer making up the recording medium for the printer contains a
binder resin in addition to the above-mentioned interlayer compounds. As the binder
resin, hydrophilic resins having the operation of increasing the dispersibility of
the interlayer compound in the dye fixation layer and for permeating the solvent for
the aqueous ink, such as water or alcohol, may be used.
[0049] As the binder resin, any ordinary thermoplastic resins may be used. These thermoplastic
resins may be exemplified by acetalized vinyl alcohols, such as polyvinyl butyral
resins, cellulose-based resins, such as hydroxy propyl cellulose resins, polyvinyl
pyrrolidone based resins, such as pyrrolidone-vinyl acetate copolymers, polyvinyl
alcohol resins and polyvinyl acetal resins. These binder resins may be used alone
or in combination. Those binder resins having substituents instigating flocculation
in the binder resins or inhibiting image fixation, such as groups more liable to be
ion-exchanged and held than the water-soluble dyes, are not preferred.
[0050] The layer thickness of the dye fixation layer is usually 2 to 40 µm and preferably
4 to 15 µm.
[0051] As the ink absorbing layer, formed on the above-mentioned dye fixation layer, hydrophilic
resins, permeated through by solvents for the aqueous ink used in the recording method
of the present invention, such as water or alcohol, are used.
[0052] As the ink absorbing resins, hydroxy propyl cellulose based resins, polyamide resins,
polyvinyl pyrrolidone based resins, polyvinyl alcohol based resins or polyvinyl butyral
based resins, may be used. These ink absorbing resins may be used alone or in combination.
[0053] The layer thickness of the ink absorbing layer is usually 1 to 5 µm and preferably
0.5 to 1.5 µm. If the layer thickness of the ink absorbing layer is not more than
0.1 µm, absorption of the aqueous ink falls short, whereas, if the layer thickness
is above 5 µm, the aqueous ink is absorbed by the ink absorbing layer to lower the
permeating properties of the ink in the interlayer compound used for accepting and
holding the dye.
EXAMPLES
[0054] The present invention will be hereinafter explained with reference to Examples based
on experimental results. These Examples are merely illustrative and are not intended
fro limiting the invention.
Experiment 1
[0055] In the experiment 1, a recording medium for a printer, comprised of an interlayer
compound 4 and an organic acid 5 contained in a dye fixation layer 2 provided on a
substrate 1, was readied, as shown in Fig.2, while an ink containing a direct dye
and an acidic dye as the water-soluble dye, was readied. Using these, an image recorded
on a recording medium for a printer was checked as to durability.
Sample 1
[0056] First, as a binder resin, 4 g of a polyvinyl alcohol resin (manufactured by NIPPON
GOSEI KAGAKU under a trade name of KH-20, were added to and dissolved in a mixed solvent
of 14 g of ethyl alcohol and 64 g of water. To this solution was added hydrotalcite
treated with an organic acid (4 g of hydrotalcite manufactured by KYOWA KAGAKU under
the trade name of KW2200 to which was adsorbed 2.5 g equivalent of malic acid), as
an interlayer compound 4, and the resulting mass was subjected to dispersion processing
for eight hours in a sand mill to produce a liquid dispersion designed for forming
the dye fixation layer. Then, 0.8 g of phthalic acid as the organic acid 5 was dissolved
in this liquid dispersion adapted for forming the dye fixation layer.
[0057] The liquid dispersion adapted for forming the dye fixation layer, thus produced,
was coated on a transparent polyester film substrate 125 µm in thickness (manufactured
by TORAY under the trade name of 'Lumilar-T-60) to a dry thickness of 4 µm. The resulting
product was dried under a condition of 100°C and one minute for completing the dye
fixation layer 2.
[0058] Then, 1.6 g of hydroxy propyl cellulose (manufactured by NIPPON SODA under the trade
name of HPC-L) were dissolved in 90 g of ethyl alcohol to produce a solution designed
for forming an ink absorbing layer. This solution for forming an ink absorbing layer
was coated by a wire bar to a dry thickness of 1 µm on the dye fixation layer 2 and
dried to form the ink absorbing layer 3. This completed a recording medium for a printer
(sample 1).
Samples 2 to 6
[0059] A liquid dispersion for the dye fixation layer was prepared using p-toluene sulfonic
acid, benzene sulfinic acid, ethyl acetoacetate, phthalimide and benzaldoxim in place
of phthalic acid. Five samples (samples 2 to 6) were fabricated in otherwise the same
way as in sample 1.
Sample 7
[0060] A recording medium for a printer (sample 7) was prepared in the same way as in sample
1, except that the liquid dispersion for forming the dye fixation layer 2 was prepared
using a mixed organic acid of phthalic acid/malic acid = 2:1.
Sample 8
[0061] A recording medium for a printer (sample 8) was prepared in the same way as in sample
1, except that the amount of addition of dissolved phthalic acid was changed to 0.24
g for preparing the liquid dispersion designed for forming the dye fixation layer
2.
Sample 9
[0062] A recording medium for a printer (sample 9) was prepared in the same way as in sample
1, except that phthalic acid was removed from the liquid dispersion adapted for forming
the dye fixation layer employed in the sample.
Sample 10
[0063] A recording medium for a printer (sample 10) was prepared in the same way as in sample
1, except that the amount of addition of dissolved phthalic acid was changed to 4.4
g, for preparing the liquid dispersion for forming the dye fixation layer 2.
Evaluation of Experiment 1
[0064] Printing samples were recorded on the recording mediums for the printer of the samples
1 to 10 prepared as described above, using an ink jet printer manufactured by SEIKO
EPSON under the trade name of MJ-800C for forming an image. The luster, water-proofness,
ink fixation and light-fastness of the recording mediums for the printer were checked
as now explained.
(1) Test for Luster
[0065] The luster of the substrate after formation of the dye fixation layer 2 was measured
by a gloss-meter manufactured by NIPPON DENSYOKU KOGYO KK under the trade name of
VG-1D, under the condition of an incidence reflection angle of 45°, using a transparent
polyester substrate prior to formation of the dye fixation layer 2 as a reference.
The results are shown in Table 1.
(2) Test for Water-Proofness
[0066] After immersing the recording medium for the printer, having the image formed thereon,
in water in its entirety for ten minutes, the recording medium was hoisted from the
water, and changes n the dye fixation layer 2 were observed visually and evaluated
in accordance with the following standard. The results are also shown in Fig.1.
- ○:
- no changes seen in the dye fixation layer
- X:
- the dye fixation layer was peeled from the substrate or dissolved such that the product
could not be used as the recording medium for a printer
(3) Test on Ink Absorptivity
[0067] During image formation, it was checked visually whether the ink was permeated into
and absorbed by the dye fixation layer 2 and the state of ink permeation and absorption
was evaluated in accordance with the following standards. The results are shown in
Table 1.
- ○:
- the ink was permeated into and absorbed by the dye fixation layer
- X:
- the ink was not permeated into nor absorbed by the dye fixation layer (4) Test on
Ink Fixation
[0068] During the test on water-proofness, changes in the image were checked visually and
evaluated in accordance with the following standards. The results are shown in Table
1.
- ○:
- no changes ae caused in an image
- △:
- the image suffers from bleeding but is practically not inconvenient
- X:
- the image suffers from significant flowing or bleeding
(5) Test on light-fastness
[0069] For each image formed in each sample, *L, *a and *b, provided in JIS Z8105, were
measured by a spectrometer manufactured by GRTAG under the trade name of SPM100-11.
[0070] Next, each sample carrying the above image was irradiated with an energy of 90 kJ/m
2 by WEATHER-OMETER manufactured by ATLAS for 72 hours for measuring *L, *a and *b
of the image of each sample irradiated with the energy.
[0071] After irradiation with the energy, the color difference △E in each sample was found
in accordance with the following equation (1):

where △*L, △*a and △*b stand for differences of *L, *a and *b before and after test,
respectively and
- ○:
- △E ≤ 5
- △:
- 5 < △E ≤ 5
- X:
- △E > 15.
TABLE 1
|
luster |
water-proofness |
ink absorption |
ink fixation |
light-fastness |
sample 1 |
92 |
○ |
○ |
○ |
○ |
sample 2 |
89 |
○ |
○ |
○ |
○ |
sample 3 |
90 |
○ |
○ |
○ |
○ |
sample 4 |
92 |
○ |
○ |
○ |
○ |
sample 5 |
91 |
○ |
○ |
○ |
○ |
sample 6 |
88 |
○ |
○ |
○ |
○ |
sample 7 |
90 |
○ |
○ |
○ |
○ |
sample 8 |
92 |
○ |
○ |
○ |
○ |
sample 9 |
90 |
X |
○ |
△ |
△ |
sample 10 |
53 |
X |
X |
X |
△ |
[0072] It is seen from the results of Table 1 that the recording mediums for a printer of
samples 1 to 8, containing one or more organic acids in the dye fixation layer containing
in turn the interlayer compound 4 are significantly superior in water-proofness, ink
fixation and light-fastness to the recording medium for a printer of the sample 9
not containing the organic acid 5. However, it is not desirable that the dye fixation
layer contain the organic acid in an amount exceeding 100 wt% based on the weight
of the interlayer compound, as in the sample 10, because then the properties as the
recording medium for the printer are deteriorated.
[0073] It is seen from the above results that, if a pre-set amount of the organic acid is
contained in the dye fixation layer 2, not only the ink fixation and water-proofness,
but also the light-fastness of an image is improved.
Experiment 2
[0074] In the experiment 2, a recording medium for a printer, containing an interlayer compound
4 in a dye fixation layer 2 on a substrate 1 and also containing an organic acid 5
in an ink absorbing layer 3 was readied, while an ink containing a direct dye and
an acidic dye as the water-soluble dye was readied. Using these, an image recorded
on the recording medium for the printer was checked.
Sample 11
[0075] First, as a binder resin, 4 g of a polyvinyl alcohol resin (manufactured by NIPPON
GOSEI KAGAKU under a trade name of KH-20, were added to and dissolved in a mixed solvent
of 14 g of ethyl alcohol and 64 g of water. To this solution was added hydrotalcite
treated with an organic acid (4 g of hydrotalcite manufactured by KYOWA KAGAKU under
the trade name of KW2200 to which was adsorbed 2.5 g equivalent of malic acid), as
an interlayer compound 4, and the resulting mass was subjected to dispersion processing
for eight hours in a sand mill to produce a liquid dispersion adapted for forming
the dye fixation layer.
[0076] The liquid dispersion adapted for forming the dye fixation layer, thus produced,
was coated on a transparent polyester film substrate 125 µm in thickness (manufactured
by TORAY under the trade name of 'Lumilar-T-60) to a dry thickness of 4 µm. The resulting
product was dried under a condition of 100°C and one minute for completing the dye
fixation layer 2.
[0077] Then, 1.6 g of hydroxy propyl cellulose (manufactured by NIPPON SODA under the trade
name of HPC-L) and 0.96 g of phthalic acid as the organic acid 5 were dissolved in
90 g of ethyl alcohol to produce a solution for forming an ink absorbing layer. This
solution for forming an ink absorbing layer was coated by a wire bar to a dry thickness
of 1 µm on the dye fixation layer 2 and dried to form the ink absorbing layer 3. This
completed a recording medium for a printer (sample 11).
Samples 12 to 16
[0078] A solution for the ink absorbing layer 3 was prepared using p-toluene sulfonic acid,
benzene sulfinic acid, ethyl acetoacetate, phthalimide and benzaldoxim in place of
phthalic acid. Five samples (samples 12 to 16) were fabricated in otherwise the same
way as in sample 1.
Sample 17
[0079] A recording medium for a printer (sample 17) was prepared in the same way as in sample
11, except that the liquid dispersion for forming the dye fixation layer 2 was prepared
using a mixed organic acid of phthalic acid/malic acid = 2:1.
Sample 18
[0080] A recording medium for a printer (sample 18) was prepared in the same way as in sample
11, except that the amount of addition of dissolved phthalic acid was changed to 0.24
g for preparing the solution for forming the ink absorbing layer.
Sample 19
[0081] A recording medium for a printer (sample 19) was prepared in the same way as in sample
11, except that phthalic acid was removed from the solution for forming the dye fixation
layer employed in the sample 11.
Sample 20
[0082] A recording medium for a printer (sample 20) was prepared in the same way as in sample
11, except that the amount of addition of dissolved phthalic acid was changed to 3.2
g for preparing the liquid dispersion for forming the dye fixation layer.
Evaluation of Experiment 2 Printing samples were recorded on the recording mediums for the printer of the samples
11 to 20 prepared as described above, using an ink jet printer for forming images.
The luster, water-proofness, ink fixation and light-fastness of the recording mediums
for the printer were checked, as in experiment 1. The results are shown in Table 2.
TABLE 2
|
luster |
water-proofness |
ink absorption |
ink fixation |
light-fastness |
sample 11 |
92 |
○ |
○ |
○ |
○ |
sample 12 |
90 |
○ |
○ |
○ |
○ |
sample 13 |
89 |
○ |
○ |
○ |
○ |
sample 14 |
90 |
○ |
○ |
○ |
○ |
sample 15 |
92 |
○ |
○ |
○ |
○ |
sample 16 |
91 |
○ |
○ |
○ |
○ |
sample 17 |
92 |
○ |
○ |
○ |
○ |
sample 18 |
90 |
○ |
○ |
○ |
○ |
sample 19 |
90 |
X |
○ |
△ |
△ |
sample 20 |
54 |
X |
X |
X |
△ |
[0083] It is seen from the results of Table 2 that the recording mediums for a printer of
samples 11 to 18, containing one or more organic acids in the ink absorbing layer
3, are significantly superior in water-proofness, ink fixation and light-fastness
to the recording medium for a printer of the sample 19 not containing the organic
acid 5. However, it is not desirable that the dye fixation layer contain the organic
acid in an amount exceeding 100 wt% based on the weight of the interlayer compound,
as in the sample 20, because then the properties as the recording medium for the printer
are deteriorated.
[0084] It is seen from the above results that, if a pre-set amount of the organic acid is
contained in the ink absorbing layer 3, not only the ink fixation and water-proofness,
but also the light-fastness of an image is improved.
Experiment 3
[0085] In the experiment 3, a recording medium for a printer, containing an interlayer compound
4 and an organic acid 5 in a dye fixation layer 2 on a substrate 1 and also containing
an organic acid 5 in an ink absorbing layer 3, was readied, while an ink containing
a direct dye and an acidic dye as the water-soluble dye was also readied. Using these,
an image recorded on the recording medium for the printer was checked.
Sample 21
[0086] In preparing a liquid dispersion for a dye fixation layer, 0.8 g of phthalic acid
was dissolved, whereas, for preparing a solution for forming an ink absorbing layer,
0.96 g of phthalic acid was dissolved. Using these, a recording medium for a printer
(sample 21) was prepared.
Sample 22
[0087] In preparing a liquid dispersion for a dye fixation layer, 0.24 g of phthalic acid
was dissolved, whereas, for preparing a solution for forming an ink absorbing layer,
0.16 g of phthalic acid was dissolved. Using these, a recording medium for a printer
(sample 22) was prepared in otherwise the same way as in sample 21.
Sample 23
[0088] In preparing a liquid dispersion for a dye fixation layer and a solution for forming
an ink absorbing layer, phthalic acid was not added A recording medium for a printer
(sample 23) was prepared in otherwise the same way as in sample 21.
Sample 24
[0089] In preparing a liquid dispersion for a dye fixation layer, 4.4 g of phthalic acid
was dissolved, whereas, for preparing a solution for forming an ink absorbing layer,
3.2 g of phthalic acid was dissolved. A recording medium for a printer (sample 24)
was prepared in otherwise the same way as in sample 21.
Evaluation of Experiment 3
[0090] Printing samples were recorded on the recording mediums for the printer of the samples
21 to 24 prepared as described above, using an ink jet printer for forming images.
The luster, water-proofness, ink absorption, ink fixation and light-fastness of the
recording mediums for the printer were evaluated as in experiment 1. The results are
shown in Table 3.
TABLE 3
|
luster |
water-proofness |
ink absorption |
ink fixation |
light fastness |
sample 21 |
93 |
○ |
○ |
○ |
○ |
sample 22 |
90 |
○ |
○ |
○ |
○ |
sample 23 |
91 |
X |
○ |
△ |
△ |
sample 24 |
48 |
X |
X |
X |
△ |
[0091] It is seen from the results of Table 3 that the recording mediums for a printer of
samples 21 and 22, containing one or more organic acids in the dye fixation layer
2 and the ink absorbing layer 3, are significantly superior in water-proofness, ink
fixation and light-fastness to the recording medium for a printer of the sample 23
not containing the organic acid 5. However, it is not desirable that the dye fixation
layer 2 and the ink absorbing layer 3 contain the organic acid in an excess amount,
as in the sample 24, because then the properties as the recording medium for the printer
are deteriorated.
[0092] It is seen from the above results that, if a pre-set amount of the organic acid is
contained in the dye fixation layer 2 and in the ink absorbing layer 3, not only the
ink fixation and water-proofness, but also the light-fastness of an image formed on
a recording medium is improved.
[0093] It may be seen from the results of experiments 1 to 3 that, by containing one or
more organic acids in at least one of the dye fixation layer and the ink absorbing
layer, water-proofness and fixation of the recording medium and the light-fastness
of the image formed thereon may be improved significantly. However, if the content
of the organic acid is excessive, the proportion of the resin is correspondingly reduced,
thus significantly deteriorating the properties of the recording medium for the printer.