[0001] This invention relates to an ink jet recording element and a printing method using
the element. More particularly, this invention relates to a porous ink jet recording
element containing porous polymeric particles.
[0002] In a typical ink jet recording or printing system, ink droplets are ejected from
a nozzle at high speed towards a recording element or medium to produce an image on
the medium. The ink droplets, or recording liquid, generally comprise a recording
agent, such as a dye or pigment, and a large amount of solvent. The solvent, or carrier
liquid, typically is made up of water, an organic material such as a monohydric alcohol,
a polyhydric alcohol or mixtures thereof.
[0003] An ink jet recording element typically comprises a support having on at least one
surface thereof an ink-receiving or image-forming layer, and includes those intended
for reflection viewing, which have an opaque support, and those intended for viewing
by transmitted light, which have a transparent support.
[0004] While a wide variety of different types of image-recording elements for use with
ink jet devices have been proposed heretofore, there are many unsolved problems in
the art and many deficiencies in the known products which have limited their commercial
usefulness.
[0005] It is well known that in order to achieve and maintain photographic-quality images
on such an image-recording element, an ink jet recording element must:
- Be readily wetted so there is no puddling, i.e., coalescence of adjacent ink dots,
which leads to non-uniform density
- Exhibit no image bleeding
- Absorb high concentrations of ink and dry quickly to avoid elements blocking together
when stacked against subsequent prints or other surfaces
- Exhibit no discontinuities or defects due to interactions between the support and/or
layer(s), such as cracking, repellencies, comb lines and the like
- Not allow unabsorbed dyes to aggregate at the free surface causing dye crystallization,
which results in bloom or bronzing effects in the imaged areas
- Have an optimized image fastness to avoid fade from contact with water or radiation
by daylight, tungsten light, or fluorescent light
[0006] An ink jet recording element that simultaneously provides an almost instantaneous
ink dry time and good image quality is desirable. However, given the wide range of
ink compositions and ink volumes that a recording element needs to accommodate, these
requirements of ink jet recording media are difficult to achieve simultaneously.
[0007] Ink jet recording elements are known that employ porous or non-porous single layer
or multilayer coatings that act as suitable image-receiving layers on one or both
sides of a porous or non-porous support. Recording elements that use non-porous coatings
typically have good image quality but exhibit poor ink dry time. Recording elements
that use porous coatings exhibit superior dry times, but typically have poorer image
quality and are prone to cracking.
[0008] A problem with known ink jet recording elements that employ porous single layer or
multilayer coatings that act as suitable image-receiving layer is dye stability during
storage. In particular, dyes printed on to an ink jet receiver element tend to fade
due to exposure to ozone which is present in the atmosphere.
[0009] Another problem with ink jet recording elements that employ porous single layer or
multilayer coatings that act as suitable image-receiving layers is image stability
under high humidity storage conditions. In particular, dyes tend to migrate through
the image receiving layer during storage since the dye image receiving layer is hydrophilic
and tends to absorb water from the atmosphere.
[0010] Copending U.S. Patent Application S.N. 09/608,466, filed June 30, 2000, relates to
an jet recording element wherein the image-receiving layer contains porous polymeric
particles in a polymeric binder. However, there is a problem with this element in
that during preparation of the coating solution, agglomeration of the polymeric particles
occurs, which when coated, results in an element having low gloss.
[0011] JP 09207430, JP 08324101 and JP 2000/239578 relate to porous image-receiving layers
for inkjet recording elements containing inorganic particles and a poly(vinyl alcohol)
having various degrees of hydrolysis. However, there is a problem with these elements
in that the references do not disclose the degree of hydrolysis for the poly(vinyl
alcohol) necessary to provide good gloss and low cracking.
[0012] It is an object of this invention to provide an ink jet recording element that has
a fast ink dry time. It is another object of this invention to provide an ink jet
recording element that has good stability when exposed to ozone and high humidity
conditions. It is another object of the invention to provide an ink jet recording
element that has high gloss with minimal cracking.
[0013] Still another object of the invention is to provide a printing method using the above
described element.
[0014] These and other objects are achieved in accordance with the invention which comprises
an inkjet recording element comprising a support having thereon an image-receiving
layer comprising porous polymeric particles in a polymeric binder, the polymeric binder
comprising poly(vinyl alcohol) having a degree of hydrolysis of at least 95% and having
a number average molecular weight of at least 45,000.
[0015] By use of the invention, an ink jet recording element is obtained which has a good
dry time and good stability when exposed to ozone and high humidity conditions, and
has high gloss with minimal cracking.
[0016] Another embodiment of the invention relates to an ink jet printing method comprising
the steps of:
A) providing an ink jet printer that is responsive to digital data signals;
B) loading the printer with an ink jet recording element described above;
C) loading the printer with an ink jet ink composition; and
D) printing on the ink jet recording element using the ink jet ink composition in
response to the digital data signals.
[0017] The support used in the ink jet recording element of the invention may be opaque,
translucent, or transparent. There may be used, for example, plain papers, resin-coated
papers, various plastics including a polyester resin such as poly(ethylene terephthalate),
poly(ethylene naphthalate) and poly(ester diacetate), a polycarbonate resin, a fluorine
resin such as poly(tetra-fluoro ethylene), metal foil, various glass materials, and
the like. In a preferred embodiment, the support is paper or a voided plastic material.
The thickness of the support employed in the invention can be from 12 to 500 µm, preferably
from 75 to 300 µm.
[0018] The porous polymeric particles which are used in the invention are in the form of
porous beads, porous irregularly shaped particles, or are aggregates of emulsion particles.
[0019] Suitable porous polymeric particles used in the invention comprise, for example,
acrylic resins, styrenic resins, or cellulose derivatives, such as cellulose acetate,
cellulose acetate butyrate, cellulose propionate, cellulose acetate propionate, and
ethyl cellulose; polyvinyl resins such as polyvinyl chloride, copolymers of vinyl
chloride and vinyl acetate and polyvinyl butyral, polyvinyl acetal, ethylene-vinyl
acetate copolymers, ethylene-vinyl alcohol copolymers, and ethylene-allyl copolymers
such as ethylene-allyl alcohol copolymers, ethylene-allyl acetone copolymers, ethylene-allyl
benzene copolymers, ethylene-allyl ether copolymers, ethylene acrylic copolymers and
polyoxy-methylene; polycondensation polymers, such as, polyesters, including polyethylene
terephthalate, polybutylene terephthalate, polyurethanes and polycarbonates.
[0020] In a preferred embodiment of the invention, the porous polymeric particles are made
from a styrenic or an acrylic monomer. Any suitable ethylenically unsaturated monomer
or mixture of monomers may be used in making such styrenic or acrylic polymer. There
may be used, for example, styrenic compounds, such as styrene, vinyl toluene, p-chlorostyrene,
vinylbenzylchloride or vinyl naphthalene; or acrylic compounds, such as methyl acrylate,
ethyl acrylate, n-butyl acrylate, n-octyl acrylate, 2-chloroethyl acrylate, phenyl
acrylate, methyl- α-chloroacrylate, methyl methacrylate, ethyl methacrylate, butyl
methacrylate; and mixtures thereof. In another preferred embodiment, methyl methacrylate
or ethylene glycol dimethacrylate is used.
[0021] In a preferred embodiment of the invention, the porous polymeric particles are crosslinked.
They may have a degree of crosslinking of 27 mole % or greater, preferably 50 mole
%, and most preferably 100 mole %. The degree of crosslinking is determined by the
mole % of multifunctional crosslinking monomer which is incorporated into the porous
polymeric particles.
[0022] Typical crosslinking monomers which may be used in making the porous polymeric particles
employed in the invention are aromatic divinyl compounds such as divinylbenzene, divinylnaphthalene
or derivatives thereof; diethylene carboxylate esters and amides such as ethylene
glycol dimethacrylate, diethylene glycol diacrylate, and other divinyl compounds such
as divinyl sulfide or divinyl sulfone compounds. Divinylbenzene and ethylene glycol
dimethacrylate are especially preferred.
[0023] The porous polymeric particles used in this invention can be prepared, for example,
by pulverizing and classification of porous organic compounds, by emulsion, suspension,
and dispersion polymerization of organic monomers, by spray drying of a solution containing
organic compounds, or by a polymer suspension technique which consists of dissolving
an organic material in a water immiscible solvent, dispersing the solution as fine
liquid droplets in aqueous solution, and removing the solvent by evaporation or other
suitable techniques. The bulk, emulsion, dispersion, and suspension polymerization
procedures are well known to those skilled in the polymer art and are taught in such
textbooks as G. Odian in "Principles of Polymerization", 2nd Ed. Wiley (1981), and
W.P. Sorenson and T.W. Campbell in "Preparation Method of Polymer Chemistry", 2nd
Ed, Wiley (1968).
[0024] Techniques to synthesize porous polymer particles are taught, for example, in U.S.
Patents 5,840,293; 5,993,805; 5,403,870; and 5,599,889, and Japanese Kokai Hei 5[1993]-222108.
For example, an inert fluid or porogen may be mixed with the monomers used in making
the porous polymer particles. After polymerization is complete, the resulting polymeric
particles are, at this point, substantially porous because the polymer has formed
around the porogen thereby forming the pore network. This technique is described more
fully in U.S. Patent 5,840,293 referred to above. Thus, the porosity of the porous
polymeric particles is achieved by mixing a porogen with the monomers used to make
the polymeric particles, dispersing the resultant mixture in water, and polymerizing
the monomers to form the porous polymeric particles.
[0025] A preferred method of preparing the porous polymeric particles used in this invention
includes forming a suspension or dispersion of ethylenically unsaturated monomer droplets
containing the crosslinking monomer and a porogen in an aqueous medium, polymerizing
the monomer to form solid, porous polymeric particles, and optionally removing the
porogen by vacuum stripping. The particles thus prepared have a porosity as measured
by a specific surface area of 35 m
2/g or greater, preferably 100 m
2/g or greater. The surface area is usually measured by B.E.T. nitrogen analysis known
to those skilled in the art.
[0026] The porous polymeric particles may be covered with a layer of colloidal inorganic
particles as described in U.S. Patents 5,288,598; 5,378,577; 5,563,226 and 5,750,378.
The porous polymeric particles may also be covered with a layer of colloidal polymer
latex particles as described in U.S. Patent 5,279,934.
[0027] The porous polymeric particles used in this invention have a median diameter less
than 10 µm, preferably less than 1 µm, and most preferably less than 0.6 µm. Median
diameter is defined as the statistical average of the measured particle size distribution
on a volume basis. For further details concerning median diameter measurement, see
T. Allen, "Particle Size Measurement", 4th Ed., Chapman and Hall, (1990).
[0028] As noted above, the polymeric particles used in the invention are porous. By porous
is meant particles which either have voids or are permeable to liquids. These particles
can have either a smooth or a rough surface.
[0029] The image-receiving layer of the ink jet recording element of the invention may contain
a surfactant. Suitable surfactants include anionic surfactants or cationic surfactants.
[0030] As noted above, the poly(vinyl alcohol) employed in the invention has a degree of
hydrolysis of at least 95% and has a number average molecular weight of at least 45,000.
In a preferred embodiment of the invention, the poly(vinyl alcohol) has a degree of
hydrolysis of at least 98%. In another preferred embodiment of the invention, the
poly(vinyl alcohol) has a number average molecular weight of from 70,000 to 105,000.
Commercial embodiments of such a poly(vinyl alcohol) are Gohsenol ® AH-22, Gohsenol
® AH-26 and Gohsenol ® AH-17 from Nippon Gohsei.
[0031] The image-receiving layer may also contain additives such as pH-modifiers like nitric
acid, cross-linkers, rheology modifiers, surfactants, UV-absorbers, biocides, lubricants,
water-dispersible latexes, mordants, dyes, optical brighteners etc.
[0032] The image-receiving layer may be applied to one or both substrate surfaces through
conventional pre-metered or post-metered coating methods such as blade, air knife,
rod, roll, slot die, curtain, slide, etc. The choice of coating process would be determined
from the economics of the operation and in turn, would determine the formulation specifications
such as coating solids, coating viscosity, and coating speed.
[0033] The image-receiving layer thickness may range from 5 to 100 µm, preferably from 10
to 50 µm. The coating thickness required is determined through the need for the coating
to act as a sump for absorption of ink solvent. The image-receiving layer of this
invention contains from 0.20 to 10.0 g/m
2 of polymeric binder, preferably from 0.40 to 5.0 g/m
2, and 1.5 to 60 g/m
2 of porous polymeric particles, preferably from 3.0 to 30 g/m
2.
[0034] Ink jet inks used to image the recording elements of the present invention are well-known
in the art. The ink compositions used in ink jet printing typically are liquid compositions
comprising a solvent or carrier liquid, dyes or pigments, humectants, organic solvents,
detergents, thickeners, preservatives, and the like. The solvent or carrier liquid
can be solely water or can be water mixed with other water-miscible solvents such
as polyhydric alcohols. Inks in which organic materials such as polyhydric alcohols
are the predominant carrier or solvent liquid may also be used. Particularly useful
are mixed solvents of water and polyhydric alcohols. The dyes used in such compositions
are typically watersoluble direct or acid type dyes. Such liquid compositions have
been described extensively in the prior art including, for example, U.S. Patents 4,381,946;
4,239,543 and 4,781,758.
[0035] The following example further illustrates the invention.
[0036] The following elements were prepared with the image-receiving layer as described:
Element 1 of the Invention
[0037] A 10% by weight solution of water, borax (sodium tetraborate decahydrate) and a sulfonated
polyester dispersion AQ29® (Eastman Chemical Co.) with a coating surfactant Olin 10G®,
with the borax to polyester binder ratio being 33:67, was rod coated on a corona-discharge
treated resin coated paper for a total dry lay-down of 1.5 g/m
2, giving a dry lay-down of borax of 0.5 g/m
2 and a polyester binder dry lay-down of 1.0 g/m
2. The subbing layer coating was dried in a oven at 40° C for 20 minutes.
[0038] A second solution at 18% by weight comprised of porous polymeric particles, poly(ethylene
glycol dimethacrylate), and a poly(vinyl alcohol) binder, AH-26 from Nippon Gohsei,
where the ratio of porous polymer particles to PVA was 80:20, was blade coated over
the subbing layer to a dry lay-down of 40 g/m
2 and dried at 40°C for 20 minutes to provide an image-receiving layer.
[0039] The number average molecular weight of the poly(vinyl alcohol) listed in Table 2
was estimated from the viscosity of a 4% aqueous solution according to a table provided
by a commercial manufacturer of poly(vinyl alcohol). The degree of hydrolysis of the
poly(vinyl alcohol) was obtained from the manufacturer.
Element 2 of the Invention
[0040] This element was prepared the same as Element 1 except that the poly(vinyl alcohol)
in the image-receiving layer was AH-22 from Nippon Gohsei.
Element 3 of the Invention
[0041] This element was prepared the same as Element 1 except that the poly(vinyl alcohol)
in the image-receiving layer was AH-17 from Nippon Gohsei.
Control Element C-1 (Low m.w. PVA and low degree of hydrolysis)
[0042] This element was prepared the same as Element 1 except that the poly(vinyl alcohol)
in the image-receiving layer was AL-06 from Nippon Gohsei.
Control Element C-2 (Low degree of hydrolysis)
[0043] This element was prepared the same as Element 1 except that the poly(vinyl alcohol)
in the image-receiving layer was GH-23 from Nippon Gohsei.
Control Element C-3 (Low degree of hydrolysis)
[0044] This element was prepared the same as Element 1 except that the poly(vinyl alcohol)
in the image-receiving layer was GH-17 from Nippon Gohsei.
Control Element C-4 (Low degree of hydrolysis)
[0045] This element was prepared the same as Element 1 except that the poly(vinyl alcohol)
in the image-receiving layer was KH-20 from Nippon Gohsei.
Control Element C-5 (Low degree of hydrolysis)
[0046] This element was prepared the same as Element 1 except that the poly(vinyl alcohol)
in the image-receiving layer was KH-17 from Nippon Gohsei.
Testing
[0047] Each element was imaged using an Epson 870 ink jet printer and ink jet inks, Cartridge
No.T007 (black) and T008 (color), and then rated for cracking according to Table 1.
Table 1
| Rating |
Cracking Observations |
| 1 |
No visible cracks under magnification |
| 2 |
Slight micro-cracks under 10X magnification |
| 3 |
Very slight visible cracks under no magnification |
| 4 |
Heavy cracking, some flaking |
| 5 |
Heavy cracking, coating flaking off |
[0048] Each element was then measured for 60 degree gloss, using a Gardner Gloss meter.
The average gloss of cyan, magenta, yellow, red, blue, green, black, and D-min was
recorded in Table 2. Average gloss level of greater than about 35 is acceptable.
Table 2
| Element |
PVA |
Degree of Hydrolysis |
Approximate Number Average m.w. |
Cracking Rating |
Gloss |
| 1 |
AH-26 |
98 |
90,000-100,000 |
2 |
45 |
| 2 |
AH-22 |
98 |
80,000-90,000 |
2 |
43 |
| 3 |
AH-17 |
98 |
60,000-65,000 |
4 |
38 |
| C-1 |
AL-06 |
92 |
25,000-30,000 |
4 |
10 |
| C-2 |
GH-23 |
88 |
80,000-90,000 |
2 |
10 |
| C-3 |
GH-17 |
88 |
60,000-65,000 |
3 |
12 |
| C-4 |
KH-20 |
80 |
70,000-80,000 |
3 |
15 |
| C-5 |
KH-17 |
80 |
65,000-70,000 |
4 |
15 |
[0049] The above results show that the elements according to the invention having a poly(vinyl
alcohol) with the degree of hydrolysis of at least 95% and a number average molecular
weight of at least 45,000 all provide good gloss as compared to the control elements.
In addition, the elements according to invention with a degree of hydrolysis of at
least 95% and an number average molecular weight of at least 70,000 provide both in
good gloss and low cracking as compared to the control elements.