EP0331125A2 - Recording medium and ink jet recording method by use thereof - Google Patents

Recording medium and ink jet recording method by use thereof Download PDF

Info

Publication number
EP0331125A2
EP0331125A2 EP89103526A EP89103526A EP0331125A2 EP 0331125 A2 EP0331125 A2 EP 0331125A2 EP 89103526 A EP89103526 A EP 89103526A EP 89103526 A EP89103526 A EP 89103526A EP 0331125 A2 EP0331125 A2 EP 0331125A2
Authority
EP
European Patent Office
Prior art keywords
recording medium
aluminum oxide
oxide particles
ink
medium according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP89103526A
Other languages
German (de)
French (fr)
Other versions
EP0331125A3 (en
EP0331125B1 (en
Inventor
Mamoru Sakaki
Masako Shimomura
Megumi Munakata
Tomomi Nakatsugawa
Horoshi Sato
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Canon Inc
Original Assignee
Canon Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP1014042A external-priority patent/JP2694771B2/en
Priority claimed from JP1018004A external-priority patent/JPH02198889A/en
Application filed by Canon Inc filed Critical Canon Inc
Publication of EP0331125A2 publication Critical patent/EP0331125A2/en
Publication of EP0331125A3 publication Critical patent/EP0331125A3/en
Application granted granted Critical
Publication of EP0331125B1 publication Critical patent/EP0331125B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/502Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording characterised by structural details, e.g. multilayer materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5218Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays

Definitions

  • This invention relates to a recording medium suitably used for the ink jet recording method, particularly to a recording medium having excellent absorptivity and color forming characteristic of an aqueous ink, as well as excellent sharpness of the recorded image obtained.
  • the present invention relates to a recording medium which can provide a recorded image with little in-room decoloration of the image and excellent storability of the image and a recording method which can provide the above recorded image.
  • the present invention relates to a recording medium having excellent water resistance and light resistance of the recorded image, while having various characteristics as mentioned above.
  • the recording medium to be used is required to have the following characteristics, namely:
  • the problem of light resistance which has been the problem in the prior art is a problem of fading of the image by irradiation of, for example, UV-ray or visible light, etc., which is raised on any image printed on any kind of paper from papers for PPC in general or fine quality paper to coated papers for ink jet.
  • the problem of in-room decoloration as herein mentioned is a problem separate from light resistance which is raised in the image also stored in, for example, a place where no direct sunlight is irradiated, but not raised in the image printed on a non-coated paper such as paper for PPC, etc.
  • the method as disclosed in Japanese Laid-open Patent Publication No. 60-49990 is a method for improving light resistance, and no effect can be seen for in-room decoloration.
  • the problem of in-room decoloration is a problem inherent in coated paper, and it may be estimated to be a problem caused by the pigment forming the coated layer.
  • the coated paper by use of highly active silica as disclosed in Japanese Laid-open Patent Publication No. 56-185690 can give an image with high optical density, while it involves a marked problem of in-room decoloration.
  • fillers in general for paper with low specific surface area such as calcium, kaolin, talc, silica, etc. are used, although in-room decoloration may be suppressed, there is now the problem that the image density is lowered.
  • an object of the present invention is to provide a recording medium which can give an image of high quality and high resolution which is high in density of the recorded image, and yet excellent in ink absorptivity and color forming characteristic of dye.
  • Another object of the present invention is to provide a recording medium which can give a recorded image with good storability, particularly a recorded image with little deterioration due to in-room decoloration and an ink jet recording method for forming such image.
  • Still another object of the present invention is to provide a recording medium which has excellent water resistance and light resistance of the recorded image, while having various characteristics as mentioned above.
  • a recording medium comprising a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity.
  • the present invention also provides a recording medium, comprising a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity, and having a Stockigt sizing degree according to JIS-P-8122 of 0 to 15 sec.
  • the present invention also provides an ink jet recording medium which performs recording by imparting small droplets of an aqueous ink to a recording medium, wherein said aqueous ink contains an acidic dye and/or a direct dye, and said recording medium comprises a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity.
  • the present invention provides a recording medium, comprising a surface layer composed mainly of aluminum oxide particles containing polyaluminum hydroxide and/or polyaluminum chloride and a lower layer having ink absorptivity.
  • the present invention further provides a recording medium, comprising a surface layer composed mainly of aluminum oxide particles with particle sizes of 5 ⁇ m or less provided on a liquid absorptive base paper.
  • the present inventors investigated about the relationship between the pigment forming the coated layer which becomes the ink receiving layer and in-­room decoloration on the basis of recognition that in-­room decoloration is a phenomenon which does not occur on non-coated paper but is generated only on coated paper, and consequently found that the problem of in-­room decoloration can occur with difficulty when a specific pigment is used as the pigment which forms the ink receiving layer, particularly the recording surface which captures the dye.
  • the first specific feature of the recording medium of the present invention resides in that the surface layer which is the recording surface is formed mainly of aluminum oxide particles.
  • the aluminum oxide particles as herein mentioned is produced by the method generally called the Bayer method by calcining aluminum hydroxide obtained by hot caustic soda treatment of bauxite which is a natural ore. Otherwise, there can be also used those produced by the method in which metallic aluminum pellets are subjected to arc discharging in water and then the resultant aluminum hydroxide is calcined, or the method in which aluminum chloride is gasified at high temperature and oxidized in gas phase, or the method in which inorganic aluminum salt (alum, etc.) is decomposed.
  • the crystal structures of the aluminum oxide particles have been known to be transitioned depending on the temperature for heat treatment form aluminum hydroxide of the giftsite type, the boehmite type to aluminum oxide of ⁇ , ⁇ , ⁇ , ⁇ type.
  • any of these preparation methods and crystal structures may be available.
  • the purity of aluminum oxide particles may be different depending on the preparation method, the degree of purification, but those available in the present invention are not limited to one containing 99.99% of aluminum oxide (Al2O3) generally called as high purity alumina, but those containing 80 to 90% or more of Al2O3 may be sufficiently available.
  • Al2O3 aluminum oxide
  • the aluminum oxide particles to be used in the present invention should preferably have a BET specific surface area within the range of from 60 to 170 m2/g, more preferably from 90 to 170 m2/g. If the BET specific surface area of the aluminum oxide particles exceeds 170 m2/g, the in-room decoloration of the recorded image will become undesirably marked.
  • in-room decoloration of recorded image is due to oxidation decomposition of the dye, and when the dye is captured on the surface layer of the recording medium, the dye will be correspondingly susceptible to oxidation by contact with air. Particularly when the dye is captured with a pigment with large specific surface area, the contact area with air becomes the maximum, whereby the in-room decoloration is caused excessively.
  • a pigment with a specific surface area of 170 m2/g or less.
  • aluminum oxide particles among various inorganic pigments can provide an image with excellent optical density as described above remains to be not clarified, but according to the imagination by the present inventors, it may be considered because aluminum oxide particles have positive charges on their surfaces and also can readily absorb electrically acidic dyes and/or direct dyes, and the paper by use of such aluminum oxide particles can capture more dyes near the surface, namely at the surface layer of the ink receiving layer, and also because the dyes and the aluminum oxide particles are electrically bonded, and therefore the dyes existing near the surface layer are stabilized to be decomposed with difficulty, etc.
  • silica is used as the pigment forming the recording surface (surface layer)
  • the relationships between the specific surface area of silica and image density and between the specific surface area and in-room decoloration is strong, prevention of in-room decoloration and improvement of image density cannot be compatible with each other, whereby it has been difficult to improve the both at the same time.
  • the tendency of the both characteristics to be antagonistic to each other may be similar also in the case of aluminum oxide particles as silica, but when aluminum oxide particles are used, the elevating tendency of image density relative to the specific surface area of the pigment is more marked than silica, having the advantage that a desired image density can be achieved with partices having lower specific surface area (170 m2/g or less) as compared with silica. This is the reason why both prevention of in-room decoloration and improvement of image density can be improved by the present invention.
  • the aluminum oxide particles to be used in the present invention have an average particle size preferably of 5 ⁇ m or less, more preferably 3 ⁇ m or less, further preferably 1 ⁇ m or less.
  • the image density and the in-room storability can be improved to considerable extent, but yet the image density and the in-room storability have the trade-off relationship.
  • the above aluminum oxide particles having an average particle size of 5 ⁇ m or less, more preferably 3 ⁇ m or less, further preferably 1 ⁇ m or less.
  • An average particle size exceeding 5 ⁇ m is insufficient for inhibiting in-room decoloration.
  • the average particle size as herein mentioned is the particle size under the state where the ink receiving layer is formed.
  • the primary particle size of aluminum oxide particle is about 1 nm to 1 ⁇ m, particles forming no secondary particle are preferred in the present invention.
  • the average primary particle size of aluminum oxide particles should be preferably 0.5 ⁇ m or less. Those exceeding 0.5 ⁇ m have insufficient ink absorptivity.
  • the second specific feature of the present invention resides in that the recording medium of the present invention is constituted of a surface layer containing the above aluminum oxide particles and a lower layer having ink absorptivity.
  • the surface layer as herein mentioned is a layer constituting the recording surface, and cannot itself absorb and retain all the ink amount attached, but has the function of adsorbing primarily the dye in the ink and permeates most of the ink solvent to migrate it to the ink absorptive lower layer.
  • the recording medium of the present invention includes the embodiment of having a recording surface in which the pigment forming the surface layer and the fibrous material of base paper exist in mixture and/or the embodiment of having a recording surface covered with a surface layer with the maximum thickness of 20 ⁇ m, more preferably 15 ⁇ m or less.
  • a preferable amount of the surface layer coated as herein mentioned may be within the range of from 0.3 to 7 g/m2 as the total amount of the pigment.
  • the coated amount is less than 0.3 g/m2
  • there is no effect as compared with the case when no surface layer is provided while if it is provided in excess of 7 g/m2 or the maximum thickness of the surface layer exceeds 20 ⁇ m, similarly as in the case of the above recording medium (2), there ensue such problems as remarkable lowering in ink absorptivity, lowering in in-room decoloration prevention or generation of paper powder even when the above aluminum oxide particles may be used.
  • a more preferable amount of the pigment coated on the surface layer is within the range of from 1 to 7 g/m2, further preferably from 2 to 7 g/m2.
  • the maximum thickness of the surface layer as herein mentioned refers to the maximum value in the depth direction of the surface layer in the cross-­section of the recording medium, and the amount of the pigment coated is the amount of the pigment coated as the surface layer.
  • the amount of the pigment coated in the surface layer is determined according to the method of JIS-P-8128, and can be obtained as the value of the amount of the ash in the whole recording medium from which the amount of ash in the base paper is removed.
  • the surface layer is formed mainly of the above aluminum oxide particles, but may also use inorganic pigments known in the art, such as silica, aluminum silicate, magnesium silicate, calcium silicate, calcium carbonate, clay, kaolin, talc, diatomaceous earth, etc., or organic pigments such as urea resin, etc. mixed in the pigment in an amount within the range which does not exceed 20% by weight.
  • inorganic pigments such as silica, aluminum silicate, magnesium silicate, calcium silicate, calcium carbonate, clay, kaolin, talc, diatomaceous earth, etc.
  • organic pigments such as urea resin, etc. mixed in the pigment in an amount within the range which does not exceed 20% by weight.
  • the pigment for forming the surface layer as described above should desirably contain 80% by weight or more of aluminum oxide particles, and when aluminum oxide particles are contained in an amount less than 80% by weight, the image density will be lowered, and also the problem of in-room storability may not be cancelled depending on the kind of the pigment used in combination.
  • a recording medium which can satisfy the respective requisite performances can be obtained by providing a relatively minute amount of the surface layer, because it is used in combination with an ink absorptive lower layer as described below.
  • the present invention is distinct in its constitutional aspect from, for example, a prior art example comprising an ink receiving layer in an amount as much as 15 g/m2 with the use of aluminum particles having a particle size of 30 ⁇ m on a polyethyleneterephthalate film as shown in Example 2 in Japanese Laid-open Patent Publication No. 58-110287 or an example comprising aluminum particles filled internally in pulp fibers during sheet making as disclosed in Japanese Laid-open Patent Publication No. 58-110288.
  • preferable recording medium having ink absorptive lower layer in the present invention may include:
  • the embodiment (1) is the most preferred embodiment in the present invention in aspect of the problems of in-room decoloration, paper powder, etc., stability in production or cost.
  • the surface layer of this embodiment is constituted of a pigment containing the above aluminum oxide particles and a binder.
  • the binder to be used in the present invention may include water-­soluble polymers such as polyvinyl alcohol, starch, oxidized starch, cationized starch, casein, carboxymethyl cellulose, gelatin, hydroxyethyl cellulose, acrylic resin, etc. and aqueous dispersion type polymers such as SBR latex, polyvinyl acetate emulsion, etc. known in the art, which can be used either singly or as a mixture of two or more kinds.
  • a preferable use ratio (weight ratio) of all the pigments to the binder may be 1/4 to 20/1, more preferably 1/2 to 4/1. If the binder amount is more than 1/4, the ink absorptivity possessed by the coated layer is lowered, while if it is lower than 20/1, powder drop-off of the above pigment from the coated layer becomes undesirably excessive.
  • the base paper on which the above surface layer is provided is required to be ink absorptive, having a preferable Stockigt sizing degree of within the range of from 0 to 15 sec., more preferably from 0 to 10 sec., further preferably from 0 to 8 sec.
  • a base paper having a Stöckigt sizing degreee in excess of 15 is used, the ink absorptivity of the recording medium as a whole is undesirably deficient.
  • the recording medium having the above coated layer provided on the base paper should desirably have a Stöckigt sizing degree within the range of from 0 to 15 sec., more preferably from 0 to 10 sec., further preferably from 0 to 5 sec. If it exceeds 15 sec., most of ink absorptivity depend on the coated layer within the above range, whereby ink absorptivity will be deficient.
  • the pulp constituting the base paper is not particularly limited, but it may be composed mainly of wood pulp as represented by LBKP or NPKP known in the art, but synthetic fibers or glass fibers may be also mixed therein, if desired.
  • fillers in the base paper to be used in the present invention may include clay, talc, kaolinite, titanium oxide, calcium carbonate, etc. generally employed, and particularly in the present invention, these fillers are contained in an amount of 1 to 20 g/m2, more preferably 2 to 10 g/m2 as calculated on the ash content.
  • calcium carbonate is particularly preferable, because the dot shape and the color forming characteristic become good.
  • the ash content in the base paper in the above embodiment (1) can be determined by, for example, eliminating the ink receiving layer from the recording medium by use of a good solvent for the binder and determining only the ash content in the base paper according to the method of JIS-P-8128, as the mass of the ash content per unit area of the paper at that time.
  • a good solvent for the binder for example, polyvinyl alcohol is used as the binder, and in this case, the coated layer is eliminated by dipping the recording medium in stationary hot water, and then the ash content as the base paper can be determined.
  • the base paper to be used in the above embodiment (1) can be made with the use of the above materials optionally together with sheet making aids, sizing agents, yield enhancers, paper force strengthening agents, etc. known in the art, if desired.
  • a preferable basis weight of the base paper to be used in the embodiment (1) may be within the range of from 60 to 120 g/m2.
  • the recording medium of the embodiment (1) absorbs ink through the base paper, if the basis weight of the base paper is less than 60 g/m2, there may ensue problems such as generation of strike-through or cockling, etc. when high density printing is performed. On the contrary, if it exceeds 120 g/m2, the paper becomes too firm, whereby a problem is involved in conveyability within the recording device.
  • the recording medium of the embodiment (2) absorbs ink only with the pigment layer, and therefore is excellent in ink absorptivity and dot shape, thus being suitable for providing images of high resolution and high quality.
  • the ink receiving layer comprises a layer constitution of two or more layers and contains an ink holding layer formed primarily of a pigment with larger particle size than the above aluminum oxide particles.
  • the ink holding layer is preferably formed mainly of a pigment having an (average) particle size of 5 to 30 ⁇ m, more preferably a silicon containing type pigment, further preferably a synthetic silica, and is arranged lower than the layer containing the aluminum oxide particles constituting the recording surface as described above.
  • the specific surface area of the pigment forming the ink holding layer should be preferably larger than the pigment forming primarily the surface layer, more preferably 200 m2/g or higher, also in aspect of ink absorptivity. Also, in aspect of color forming characteristic and ink absorptivity, a constitution with the ink absorption speed of the surface layer which is slow to the extent that ink droplets may be blurred in appropriate sizes and with the ink absorptivity of the ink holding layer being large is preferable.
  • the use ratio of the pigment to the binder in the surface layer constituting the recording surface may be preferably 1/3 to 5/1, more preferably 1/2 to 3/1, preferably 1/1 to 10/1 as the total of the ink receiving layer.
  • any of the binders known in the art can be used for formation of the ink holding layer.
  • the amount of the total ink receiving layer coated may be preferably within the range of from 2 to 50 g/m2, more preferably from 8 to 30 g/m2, with the coated amount of the ink holding layer being preferably larger than that of the surface layer.
  • porous silica particles having spherical particle shapes as disclosed in Japanese Laid-open Patent Publication No. 62-183382 can be used.
  • an ink receiving layer with higher void volume as compared with that by use of amorphous pigment of the prior art can be formed, whereby a recording medium having excellent ink absorptivity can be provided.
  • a coating solution containing the components as described above is coated on the substrate surface according to the method known in the art, such as the roll coater method, the blade coater method, the air knife coater method, the gate roll coater method, the size press method, etc.
  • the coating can be dried according to the method known in the art by using, for example, hot air drying furnace, hot drum, etc. to give the recording medium of the present invention.
  • a supply calender may be used in the steps.
  • the recording medium of the present invention formed as described above has high image density, excellent ink absorptivity and yet excellent characteristics without occurrence of in-room decoloration.
  • the polyaluminum hydroxide as herein mentioned is a compound having two or more compounds represented by [Al(OH) 3-a ] in the molecule, including, for example, compounds represented by: [Al(OH)3] n AlCl3 (n ⁇ 2), and the above compounds are commercially availabe under the trade name of paho#2S from Asada Kagaku Kogyo.
  • the polyaluminum chloride is a compound having two or more compounds represented by [AlCl 3-b ] in the molecule, including, for example, compounds represented by the formula: [Al2(OH)1Cl 6-l ] m (m ⁇ 1), and the compounds are commercially available under the trade name of PAC from Taki Kagaku Kogyo.
  • the recording medium of the present invention should preferably contain these compounds in an amount within the range of from 0.01 g/m2 to 5 g/m2. If it is less than 0.01 g/m2, water resistance is insufficient, while if it is contained in excess of 5 g/m2, there are problems such as lowering in ink absorptivity and image density.
  • the recording medium of the present invention which uses an aluminum type compound as different from the amine type as in the prior art as the dye fixing agent, has the effect of improving water resistance of the dye, and also has no deleterious effect on light resistance.
  • the polyaluminum compound can be used with an amine type dye fixing agent as described above mixed therein, the amine type water resistant agent in this case should be preferably within the range of 70% by weight or less, more preferably 25% by weight or less, of the polyaluminum compound. If it is contained in excess of 70%, the bad influence by use of the amine type water resistance-affording agent will appear to lower undesirably light resistance.
  • the ink receiving layer may also contain fluorescent brighteners, surfactants, defoaming agents, pH controllers, antifungal agents, UV-absorbers, antioxidants, etc., if necessary.
  • the ink jet recording system for the recording medium of the present invention with a constitution as described above, for example, according to the recording method of the present invention which performs recording with a multi-colr aqueous ink such as yellow (Y), magenta (M), cyan (C), black (Bk), etc., no in-room decoloration occurs on the image obtained to give a recorded image with excellent storability.
  • a multi-colr aqueous ink such as yellow (Y), magenta (M), cyan (C), black (Bk), etc.
  • the method of the present invention is a recording method by use of the recording medium of the present invention as described above, and the ink itself which is imparted by the ink jet recording method to the specific recording medium as described above in the recording method may be also known.
  • its recording agent may be water soluble dyes as represented by direct dyes, acidic dyes, basic dyes, reactive dyes, dyes for foods, etc.
  • the dyes particularly suitable for the ink in the ink jet recording system which can give images satisfying requisite performances in combination with the above recording medium such as color forming characteristic, sharpness, stability, light resistance and others may include: Direct dyes such as C.I. Direct Black 17, 19, 32, 51, 71, 108, 146, C.I.
  • dyes set forth above are particularly preferred for the ink applicable to the recording method of the present invention, and the dyes for the ink to be used in the present invention are not limited to these dyes.
  • Such water soluble dyes are used generally in the ink of the prior art at a ratio about 0.1 to 20% by weight of the ink, and the same ratio may be used also in the present invention.
  • the solvent to be used for the aqueous ink to be used in the present invention is water or a solvent mixture of water with a water soluble organic solvent, particularly preferably a solvent mixture of water and a water soluble organic solvent.
  • a water soluble organic solvent one containing a polyhydric alcohol having drying prevention effect on ink is preferred.
  • the water it is preferable to use deionized water instead of water in general containing various ions.
  • the content of the water soluble organic solvent in the ink may be generally within the range of from 0 to 95% by weight, preferably from 2 to 80% by weight, more preferably from 5 to 50% by weight.
  • a preferable water content may be 20 to 98%, more preferably 50 to 90%, based on the total weight of the ink.
  • the ink to be used in the present invention can also include surfactants, viscosity controllers, surface tension controllers, etc., if desired, in addition to the above components.
  • the method of performing recording by imparting the above ink to the above recording medium in the method of the present invention may be any recording method, but preferably the ink jet recording method, and said method may be any system, provided that it is a system capable of eliminating effectively the ink from the nozzle and imparting the ink to the recording medium which is the target of injection.
  • the ink jet system which discharges ink through nozzle by the acting force due to the state change by the abrupt volume change of ink having received the action of heat energy according to the method disclosed in Japanese Laid-open Patent Publication No. 54-59936 can be effectively used.
  • the recording medium of the present invention as described above is suitable as the recording medium for ink jet recording, particularly by use of aqueous ink, and exhibits the following effects.
  • a coating solution having the composition shown below was coated according to the bar coater method to a coated amount on drying of 5 g/m2 and dried at 110 °C for 3 minutes to obtain a recording medium of the present invention.
  • the pigments used are shown below in Table 1.
  • a recording medium was prepared in the same manner as in Example 1 except for using a paper for PPC having a Stöckigt sizing degree of 24 sec. and a basis weight of 66 g/m2 (paper for Canon NP dry) as the base paper.
  • a coating solution with the same composition as in Example 1 was coated by the bar coating method to a coated amount on drying of 7 g/m2 and dried at 110 °C to obtain the recording media of the present invention and Comparative example.
  • the mixtures of alumina with other pigments as shown in Table 2 were used.
  • Table 2 I II III IV Example 5 24 parts 0 parts 4.8 (g/m2) 1 (sec)
  • Example 6 20 4 4.8 1 Comparative example 2 0 24 4.5 1 Remarks I .... Alumina (AKP-G, Sumitomo Kagaku) II .... Zinc oxide (active zinc white AZO, produced by Seido Kagaku, Particle size 0.8 ⁇ m, specific surface area 64 m2/g) III ... Amount of pigment coated (g/m2) IV ....
  • the ink jet recording adaptability of the above recording medium was evaluated by performing the ink jet recording with an ink having the composition shown below by means of an ink jet printer having ink jet heads equipped with 128 nozzles with nozzle interval of 1 mm/16 nozzles corresponding to the four colors of Y, M, C and Bk.
  • Synthetic silica (spherical silica, BET specific surface area 700m2/g, average particle size 20 ⁇ m, produced by Asahi Glass) 18 parts Polyvinyl alcohol (PVA-117/R-1130, produced Kuraray) 6 parts Water 76 parts
  • Porous alumina RG-40, produced by Iwatani Kagaku Kogyo specific surface area 48m2/g
  • Fine particulate alumina (Aerosil, aluminum oxide-C, produced by Nihon Aerosil, BET specific surface area 100m2/g) 13 parts Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts Water 77 parts
  • Fine powder silica (Syloid 74, produced by Fujidevison, BET specific surface area 300m2/g) 13 parts Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts Water 77 parts
  • Zinc oxide active zinc white AZO, produced by Seido Kagaku BET specific surface area 64m2/g
  • Polyvinyl alcohol PVA-110, produced by Kuraray 10 parts Water 77 parts
  • Example 9 On the same base paper as in Example 9, by use of a coating solution III shown below, it was coated by the bar coater method to a coated amount on drying of 20 g/m2, followed by drying at 110 °C for 5 minutes, to form an ink holding layer, and on the ink holding layer was coated a coating solution IV shown below to a coated amount on drying of 7 g/m2, followed by drying at 110 °C for 3 minutes to form a surface layer, thus providing a recording medium of the present invention.
  • a coating solution III shown below it was coated by the bar coater method to a coated amount on drying of 20 g/m2, followed by drying at 110 °C for 5 minutes, to form an ink holding layer, and on the ink holding layer was coated a coating solution IV shown below to a coated amount on drying of 7 g/m2, followed by drying at 110 °C for 3 minutes to form a surface layer, thus providing a recording medium of the present invention.
  • Example 10 On the same base paper as used in Example 10 was coated a coating solution shown below by the bar coated method to a coated amount of 15 g/m2, followed by drying at 140 °C for 5 minutes to form a lower layer with low ink absorptivity. On the lower layer was applied coating by use of the coating solution used in Example 10 in the same manner as in Example 10, followed by drying, to obtain a recording medium 6 for comparison.
  • Pigment 20 Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts Water-resistant agent 3.6 parts Water 266 parts
  • Light resistance was evaluated by irradiating the printed product of (1) by use of Xenon Fade-Ometer (manufactured by Ci-35 Atlas Co.) under the conditions of a black panel temperature of 63 °C and a humidity of 70% RH for 100 hours, and determining the ratio of the image density at the M printed portion after irradiation relative to the image density before irradiation.
  • Example 13 o 1.60 95% 83% 3.4 14 o 1.48 94% 78% 2.3 15 o 1.59 98% 80% 3.2 16 o 1.48 99% 74% 2.1 Reference Example 1 o 1.62 72% 88% 4.4 Comparative Example 7 o 1.63 80% 76% 26.3 8 o 1.59 102% 43% 3.1 9 o 1.48 99% 38% 1.9

Landscapes

  • Ink Jet Recording Methods And Recording Media Thereof (AREA)
  • Ink Jet (AREA)
  • Particle Formation And Scattering Control In Inkjet Printers (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Prostheses (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • External Artificial Organs (AREA)
  • Paper (AREA)

Abstract

A recording medium comprises a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity. A recording medium comprises a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity, and having a Stöckigt sizing degree according to JIS-P-8122 of 0 to 15 sec. An ink jet recording method performs recording by imparting small droplets of an aqueous ink to a recording medium, wherein said aqueous ink contains an acidic dye and/or a direct dye, and said recording medium comprises a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity. A recording medium comprising a surface layer composed mainly of aluminum oxide particles containing polyaluminum hydroxide and/or polyaluminum chloride and a lower layer having ink absorptivity. A recording medium comprises a surface layer composed mainly of aluminum oxide particles having particle sizes of 5 µm or less provided on a liquid absorptive base paper.

Description

    BACKGROUND OF THE INVENTION Field of the Invention
  • This invention relates to a recording medium suitably used for the ink jet recording method, particularly to a recording medium having excellent absorptivity and color forming characteristic of an aqueous ink, as well as excellent sharpness of the recorded image obtained.
  • Further, the present invention relates to a recording medium which can provide a recorded image with little in-room decoloration of the image and excellent storability of the image and a recording method which can provide the above recorded image.
  • Further, the present invention relates to a recording medium having excellent water resistance and light resistance of the recorded image, while having various characteristics as mentioned above.
  • Related Background Art
  • In the prior art, as the recording medium for ink jet recording, there have been known:
    • (1) one obtained by making paper in general composed mainly of pulp into a sheet with low sizing degree like filter paper or blotting paper;
    • (2) one having an ink absorbing layer by the use of a porous inorganic pigment provided on a base paper with low ink absorbtivity such as usual paper of fine quality, etc., as disclosed in Japanese Laid-open Patent Publication No.56-148585, etc.
  • On the other hand, in the ink jet recording system for which formation of a color image of high quality and high resolution is particularly demanded, the recording medium to be used is required to have the following characteristics, namely:
    • (1) good color forming characteristic of the ink attached on the recording medium;
    • (2) good true sphericity of the ink dot;
    • (3) good ink absorption capacity such that the ink attached will not flow out even when a plurality of ink droplets may be attached on the same spot;
    • (4) good ink fixability such that the ink droplets attached will not be blurred even when they may be rubbed immediately after attachment;
    • (5) good image storability of the image formed such as water resistance, light resistance, etc.
  • However, no recording medium which satisfies all of the above requisite performances has been known yet.
  • Particularly, recently, the problem of in-room decoloration of the recorded image inherent in coated paper has been taken a close-up.
  • The problem of light resistance which has been the problem in the prior art is a problem of fading of the image by irradiation of, for example, UV-ray or visible light, etc., which is raised on any image printed on any kind of paper from papers for PPC in general or fine quality paper to coated papers for ink jet. However, the problem of in-room decoloration as herein mentioned is a problem separate from light resistance which is raised in the image also stored in, for example, a place where no direct sunlight is irradiated, but not raised in the image printed on a non-coated paper such as paper for PPC, etc.
  • For example, the method as disclosed in Japanese Laid-open Patent Publication No. 60-49990 is a method for improving light resistance, and no effect can be seen for in-room decoloration. Thus, the problem of in-room decoloration is a problem inherent in coated paper, and it may be estimated to be a problem caused by the pigment forming the coated layer.
  • For example, the coated paper by use of highly active silica as disclosed in Japanese Laid-open Patent Publication No. 56-185690 can give an image with high optical density, while it involves a marked problem of in-room decoloration. On the contrary, if fillers in general for paper with low specific surface area such as calcium, kaolin, talc, silica, etc. are used, although in-room decoloration may be suppressed, there is now the problem that the image density is lowered.
  • Thus, particularly the problems of in-room decoloration and image density are antagonistic to each other, and they have been problems not solved by the prior art technique.
  • SUMMARY OF THE INVENTION
  • Accordingly, an object of the present invention is to provide a recording medium which can give an image of high quality and high resolution which is high in density of the recorded image, and yet excellent in ink absorptivity and color forming characteristic of dye.
  • Another object of the present invention is to provide a recording medium which can give a recorded image with good storability, particularly a recorded image with little deterioration due to in-room decoloration and an ink jet recording method for forming such image.
  • Still another object of the present invention is to provide a recording medium which has excellent water resistance and light resistance of the recorded image, while having various characteristics as mentioned above.
  • The above and other objects of the present invention can be accomplished by the inventions as specified below.
  • According to the present invention, there is provided a recording medium, comprising a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity.
  • The present invention also provides a recording medium, comprising a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity, and having a Stockigt sizing degree according to JIS-P-8122 of 0 to 15 sec.
  • The present invention also provides an ink jet recording medium which performs recording by imparting small droplets of an aqueous ink to a recording medium, wherein said aqueous ink contains an acidic dye and/or a direct dye, and said recording medium comprises a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity.
  • Further, the present invention provides a recording medium, comprising a surface layer composed mainly of aluminum oxide particles containing polyaluminum hydroxide and/or polyaluminum chloride and a lower layer having ink absorptivity.
  • The present invention further provides a recording medium, comprising a surface layer composed mainly of aluminum oxide particles with particle sizes of 5 µm or less provided on a liquid absorptive base paper.
  • The present inventors investigated about the relationship between the pigment forming the coated layer which becomes the ink receiving layer and in-­room decoloration on the basis of recognition that in-­room decoloration is a phenomenon which does not occur on non-coated paper but is generated only on coated paper, and consequently found that the problem of in-­room decoloration can occur with difficulty when a specific pigment is used as the pigment which forms the ink receiving layer, particularly the recording surface which captures the dye.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The present invention is described in more detail by referring to preferred embodiments.
  • The first specific feature of the recording medium of the present invention resides in that the surface layer which is the recording surface is formed mainly of aluminum oxide particles.
  • The aluminum oxide particles as herein mentioned is produced by the method generally called the Bayer method by calcining aluminum hydroxide obtained by hot caustic soda treatment of bauxite which is a natural ore. Otherwise, there can be also used those produced by the method in which metallic aluminum pellets are subjected to arc discharging in water and then the resultant aluminum hydroxide is calcined, or the method in which aluminum chloride is gasified at high temperature and oxidized in gas phase, or the method in which inorganic aluminum salt (alum, etc.) is decomposed.
  • The crystal structures of the aluminum oxide particles have been known to be transitioned depending on the temperature for heat treatment form aluminum hydroxide of the giftsite type, the boehmite type to aluminum oxide of γ, σ, η, ϑ, α type. Of course, in the present invention, any of these preparation methods and crystal structures may be available.
  • The purity of aluminum oxide particles may be different depending on the preparation method, the degree of purification, but those available in the present invention are not limited to one containing 99.99% of aluminum oxide (Al₂O₃) generally called as high purity alumina, but those containing 80 to 90% or more of Al₂O₃ may be sufficiently available.
  • The aluminum oxide particles to be used in the present invention should preferably have a BET specific surface area within the range of from 60 to 170 m²/g, more preferably from 90 to 170 m²/g. If the BET specific surface area of the aluminum oxide particles exceeds 170 m²/g, the in-room decoloration of the recorded image will become undesirably marked.
  • According to the knowledge of the present inventors, in-room decoloration of recorded image is due to oxidation decomposition of the dye, and when the dye is captured on the surface layer of the recording medium, the dye will be correspondingly susceptible to oxidation by contact with air. Particularly when the dye is captured with a pigment with large specific surface area, the contact area with air becomes the maximum, whereby the in-room decoloration is caused excessively.
  • Accordingly, in the present invention, it is preferable to use a pigment with a specific surface area of 170 m²/g or less.
  • In contrast, in the prior art, when such a pigment as silica or calcium carbonate used for ink jet recording paper having a specific surface area of 170 m²/g is used for the ink receiving layer, due to poor absorptivity of the pigment to the dye, the dye in the ink attached is perameted deep into the paper layer together with the solvent in the ink, whereby color forming characteristic of the dye and image density were insufficient, although the problem of in-­room decoloration may be solved.
  • This is the first reason why a pigment with a BET surface area of 170 m²/g or less has not been used in the prior art for the coated paper as described above.
  • Whereas, according to the knowledge of the present inventors, even a pigment with a BET specific surface area of 170 m²/g or less can give sufficient in-room decoloration inhibiting effect and also excellent image density, when aluminum oxide particles are used.
  • The reason why only aluminum oxide particles among various inorganic pigments can provide an image with excellent optical density as described above remains to be not clarified, but according to the imagination by the present inventors, it may be considered because aluminum oxide particles have positive charges on their surfaces and also can readily absorb electrically acidic dyes and/or direct dyes, and the paper by use of such aluminum oxide particles can capture more dyes near the surface, namely at the surface layer of the ink receiving layer, and also because the dyes and the aluminum oxide particles are electrically bonded, and therefore the dyes existing near the surface layer are stabilized to be decomposed with difficulty, etc.
  • On the other hand, when aluminum oxide particles not satisfying a BET specific surface area of 60 m²/g or more are used, the density of the image formed becomes insufficient and therefore it is desirable to use those having a BET specific surface area of 60 m²/g or more.
  • According to the knowledge of the present inventors, when silica is used as the pigment forming the recording surface (surface layer), since the relationships between the specific surface area of silica and image density and between the specific surface area and in-room decoloration is strong, prevention of in-room decoloration and improvement of image density cannot be compatible with each other, whereby it has been difficult to improve the both at the same time.
  • Thus, the tendency of the both characteristics to be antagonistic to each other may be similar also in the case of aluminum oxide particles as silica, but when aluminum oxide particles are used, the elevating tendency of image density relative to the specific surface area of the pigment is more marked than silica, having the advantage that a desired image density can be achieved with partices having lower specific surface area (170 m²/g or less) as compared with silica. This is the reason why both prevention of in-room decoloration and improvement of image density can be improved by the present invention.
  • The aluminum oxide particles to be used in the present invention have an average particle size preferably of 5 µm or less, more preferably 3 µm or less, further preferably 1 µm or less.
  • Thus, by use of the aluminum oxide particles having the specific surface area as specified above, the image density and the in-room storability can be improved to considerable extent, but yet the image density and the in-room storability have the trade-off relationship.
  • In other words, according to the knowledge of the present inventors, for having further excellent in-­room storability, while retaining high image density, it is preferable to use the above aluminum oxide particles, having an average particle size of 5 µm or less, more preferably 3 µm or less, further preferably 1 µm or less.
  • An average particle size exceeding 5 µm is insufficient for inhibiting in-room decoloration. The average particle size as herein mentioned is the particle size under the state where the ink receiving layer is formed. Generally speaking, since the primary particle size of aluminum oxide particle is about 1 nm to 1 µm, particles forming no secondary particle are preferred in the present invention. Further, in aspect of ink absorptivity, the average primary particle size of aluminum oxide particles should be preferably 0.5 µm or less. Those exceeding 0.5 µm have insufficient ink absorptivity.
  • Also, according to the knowledge of the present inventors, although the correlation between the particle size of the aluminum oxide particles and the image density is low, in-room storability becomes better as the particle size is smaller.
  • This may be considered to be due to the fact that the apparent surface area on the recording surface is larger when a pigment with larger particle sizes is used during formation of the recording surface as compared when particles with smaller particles are laminated, whereby the dye adsorbed is susceptible to oxidation.
  • In the recording medium of the prior art, for improving ink absorptivity, secondary particles are formed, and a pigment with such large particle size has been employed. In the present invention, there is no problem in ink absoptivity even by formation of a surface layer with particles of submicron order without formation of secondary particles, because of the special constitution of the ink receiving layer as described below.
  • The second specific feature of the present invention resides in that the recording medium of the present invention is constituted of a surface layer containing the above aluminum oxide particles and a lower layer having ink absorptivity.
  • The surface layer as herein mentioned is a layer constituting the recording surface, and cannot itself absorb and retain all the ink amount attached, but has the function of adsorbing primarily the dye in the ink and permeates most of the ink solvent to migrate it to the ink absorptive lower layer.
  • For this reason, the recording medium of the present invention includes the embodiment of having a recording surface in which the pigment forming the surface layer and the fibrous material of base paper exist in mixture and/or the embodiment of having a recording surface covered with a surface layer with the maximum thickness of 20 µm, more preferably 15 µm or less.
  • A preferable amount of the surface layer coated as herein mentioned may be within the range of from 0.3 to 7 g/m² as the total amount of the pigment. When the coated amount is less than 0.3 g/m², there is no effect as compared with the case when no surface layer is provided, while if it is provided in excess of 7 g/m² or the maximum thickness of the surface layer exceeds 20 µm, similarly as in the case of the above recording medium (2), there ensue such problems as remarkable lowering in ink absorptivity, lowering in in-room decoloration prevention or generation of paper powder even when the above aluminum oxide particles may be used.
  • In the present invention, a more preferable amount of the pigment coated on the surface layer is within the range of from 1 to 7 g/m², further preferably from 2 to 7 g/m².
  • The maximum thickness of the surface layer as herein mentioned refers to the maximum value in the depth direction of the surface layer in the cross-­section of the recording medium, and the amount of the pigment coated is the amount of the pigment coated as the surface layer. The amount of the pigment coated in the surface layer is determined according to the method of JIS-P-8128, and can be obtained as the value of the amount of the ash in the whole recording medium from which the amount of ash in the base paper is removed.
  • In the present invention, the surface layer is formed mainly of the above aluminum oxide particles, but may also use inorganic pigments known in the art, such as silica, aluminum silicate, magnesium silicate, calcium silicate, calcium carbonate, clay, kaolin, talc, diatomaceous earth, etc., or organic pigments such as urea resin, etc. mixed in the pigment in an amount within the range which does not exceed 20% by weight.
  • The pigment for forming the surface layer as described above should desirably contain 80% by weight or more of aluminum oxide particles, and when aluminum oxide particles are contained in an amount less than 80% by weight, the image density will be lowered, and also the problem of in-room storability may not be cancelled depending on the kind of the pigment used in combination.
  • As described above, in the recording medium of the present invention, a recording medium which can satisfy the respective requisite performances can be obtained by providing a relatively minute amount of the surface layer, because it is used in combination with an ink absorptive lower layer as described below.
  • The present invention, as shown above, is distinct in its constitutional aspect from, for example, a prior art example comprising an ink receiving layer in an amount as much as 15 g/m² with the use of aluminum particles having a particle size of 30 µm on a polyethyleneterephthalate film as shown in Example 2 in Japanese Laid-open Patent Publication No. 58-110287 or an example comprising aluminum particles filled internally in pulp fibers during sheet making as disclosed in Japanese Laid-open Patent Publication No. 58-110288.
  • Specific examples of preferable recording medium having ink absorptive lower layer in the present invention may include:
    • (1) the embodiment in which a surface layer is provided on an liquid absorptive base paper, and the base paper also functions as the ink absorptive lower layer; and
    • (2) the embodiment in which a pigment layer with excellent ink absorptivity is provided on a base paper, on which a surface layer is provided, etc.
  • In the following, the respective embodiments are to be described in detail.
  • The embodiment (1) is the most preferred embodiment in the present invention in aspect of the problems of in-room decoloration, paper powder, etc., stability in production or cost.
  • The surface layer of this embodiment is constituted of a pigment containing the above aluminum oxide particles and a binder. Examples of the binder to be used in the present invention may include water-­soluble polymers such as polyvinyl alcohol, starch, oxidized starch, cationized starch, casein, carboxymethyl cellulose, gelatin, hydroxyethyl cellulose, acrylic resin, etc. and aqueous dispersion type polymers such as SBR latex, polyvinyl acetate emulsion, etc. known in the art, which can be used either singly or as a mixture of two or more kinds.
  • In this embodiment, a preferable use ratio (weight ratio) of all the pigments to the binder may be 1/4 to 20/1, more preferably 1/2 to 4/1. If the binder amount is more than 1/4, the ink absorptivity possessed by the coated layer is lowered, while if it is lower than 20/1, powder drop-off of the above pigment from the coated layer becomes undesirably excessive.
  • The base paper on which the above surface layer is provided is required to be ink absorptive, having a preferable Stockigt sizing degree of within the range of from 0 to 15 sec., more preferably from 0 to 10 sec., further preferably from 0 to 8 sec. When a base paper having a Stöckigt sizing degreee in excess of 15 is used, the ink absorptivity of the recording medium as a whole is undesirably deficient.
  • The recording medium having the above coated layer provided on the base paper should desirably have a Stöckigt sizing degree within the range of from 0 to 15 sec., more preferably from 0 to 10 sec., further preferably from 0 to 5 sec. If it exceeds 15 sec., most of ink absorptivity depend on the coated layer within the above range, whereby ink absorptivity will be deficient.
  • In the present invention, the pulp constituting the base paper is not particularly limited, but it may be composed mainly of wood pulp as represented by LBKP or NPKP known in the art, but synthetic fibers or glass fibers may be also mixed therein, if desired.
  • Specific examples of the fillers in the base paper to be used in the present invention may include clay, talc, kaolinite, titanium oxide, calcium carbonate, etc. generally employed, and particularly in the present invention, these fillers are contained in an amount of 1 to 20 g/m², more preferably 2 to 10 g/m² as calculated on the ash content.
  • According to the knowledge of the present inventors, particularly blurring and dot shapes of ink droplets attached on the recording medium are greatly affected by the ash content in the base paper of this type of paper, and when the ash content is less than 1 g/m², the ink droplets attached will be blurred greatly along the fiber direction on the base paper surface, whereby the dot shapes are bad and also blurring of the ink droplets will become larger than is necessary. On the contrary, if it exceeds 20 g/m², the recording medium itself will lose firmness, and in addition thereto, powder drop-off from the base paper will occur undesirably.
  • Further, of the above fillers, calcium carbonate is particularly preferable, because the dot shape and the color forming characteristic become good.
  • The ash content in the base paper in the above embodiment (1) can be determined by, for example, eliminating the ink receiving layer from the recording medium by use of a good solvent for the binder and determining only the ash content in the base paper according to the method of JIS-P-8128, as the mass of the ash content per unit area of the paper at that time. For example, in conventional paper for ink jet, polyvinyl alcohol is used as the binder, and in this case, the coated layer is eliminated by dipping the recording medium in stationary hot water, and then the ash content as the base paper can be determined.
  • The base paper to be used in the above embodiment (1) can be made with the use of the above materials optionally together with sheet making aids, sizing agents, yield enhancers, paper force strengthening agents, etc. known in the art, if desired.
  • Also, a preferable basis weight of the base paper to be used in the embodiment (1) may be within the range of from 60 to 120 g/m². Thus, since the recording medium of the embodiment (1) absorbs ink through the base paper, if the basis weight of the base paper is less than 60 g/m², there may ensue problems such as generation of strike-through or cockling, etc. when high density printing is performed. On the contrary, if it exceeds 120 g/m², the paper becomes too firm, whereby a problem is involved in conveyability within the recording device.
  • The recording medium of the embodiment (2) absorbs ink only with the pigment layer, and therefore is excellent in ink absorptivity and dot shape, thus being suitable for providing images of high resolution and high quality.
  • The specific feature of the recording medium of the embodiment (2) resides in that the ink receiving layer comprises a layer constitution of two or more layers and contains an ink holding layer formed primarily of a pigment with larger particle size than the above aluminum oxide particles.
  • The ink holding layer is preferably formed mainly of a pigment having an (average) particle size of 5 to 30 µm, more preferably a silicon containing type pigment, further preferably a synthetic silica, and is arranged lower than the layer containing the aluminum oxide particles constituting the recording surface as described above.
  • In the above embodiment (2), by use of a pigment with larger particle sizes as the ink holding layer and embedding the small unevennesses on the surface with a pigment with smaller particle sizes of the layer constituting the recording surface, images with further better dot shape and without feeling of coarseness can be obtained without occurrence of powder drop-off, while utilizing also the advantage when using a pigment with large particle sizes.
  • The specific surface area of the pigment forming the ink holding layer should be preferably larger than the pigment forming primarily the surface layer, more preferably 200 m²/g or higher, also in aspect of ink absorptivity. Also, in aspect of color forming characteristic and ink absorptivity, a constitution with the ink absorption speed of the surface layer which is slow to the extent that ink droplets may be blurred in appropriate sizes and with the ink absorptivity of the ink holding layer being large is preferable. For this purpose, the use ratio of the pigment to the binder in the surface layer constituting the recording surface may be preferably 1/3 to 5/1, more preferably 1/2 to 3/1, preferably 1/1 to 10/1 as the total of the ink receiving layer. Also, any of the binders known in the art can be used for formation of the ink holding layer. The amount of the total ink receiving layer coated may be preferably within the range of from 2 to 50 g/m², more preferably from 8 to 30 g/m², with the coated amount of the ink holding layer being preferably larger than that of the surface layer.
  • Further, for making the ink absorptivity of the recording medium of the embodiment (2) better, preferably as the pigment forming the ink holding layer, porous silica particles having spherical particle shapes as disclosed in Japanese Laid-open Patent Publication No. 62-183382 can be used. Particularly, when the above spherical silica having an average particle size of 5 to 30 µm is used for the ink holding layer, an ink receiving layer with higher void volume as compared with that by use of amorphous pigment of the prior art can be formed, whereby a recording medium having excellent ink absorptivity can be provided.
  • In preparing the recording medium of the present invention according to the respective embodiments as described above, a coating solution containing the components as described above is coated on the substrate surface according to the method known in the art, such as the roll coater method, the blade coater method, the air knife coater method, the gate roll coater method, the size press method, etc. Also, after an aqueous coating solution comprising a pigment and a binder is coated on the substrate, the coating can be dried according to the method known in the art by using, for example, hot air drying furnace, hot drum, etc. to give the recording medium of the present invention.
  • Also, for making the ink receiving layer surface smooth, or enhancing the surface strength of the ink receiving layer, a supply calender may be used in the steps.
  • The recording medium of the present invention formed as described above has high image density, excellent ink absorptivity and yet excellent characteristics without occurrence of in-room decoloration.
  • For improving further water resistance and light resistance of the recorded image, while retaining the above various recording characteristics, it is necessary to incorporate a polyaluminum hydroxide and/or a polyaluminum chloride in the pigment layer containing the aluminum oxide particles.
  • The polyaluminum hydroxide as herein mentioned is a compound having two or more compounds represented by [Al(OH)3-a] in the molecule, including, for example, compounds represented by:
    [Al(OH)₃]nAlCl₃ (n ≧ 2),
    and the above compounds are commercially availabe under the trade name of paho#2S from Asada Kagaku Kogyo.
  • The polyaluminum chloride is a compound having two or more compounds represented by [AlCl3-b] in the molecule, including, for example, compounds represented by the formula:
    [Al₂(OH)₁Cl6-l]m (m ≧ 1),
    and the compounds are commercially available under the trade name of PAC from Taki Kagaku Kogyo.
  • The recording medium of the present invention should preferably contain these compounds in an amount within the range of from 0.01 g/m² to 5 g/m². If it is less than 0.01 g/m², water resistance is insufficient, while if it is contained in excess of 5 g/m², there are problems such as lowering in ink absorptivity and image density.
  • In the prior art, as the dye fixing agent availabe in recording medium for ink jet, there may be included those disclosed in Japanese Laid-open Patent Publications Nos. 56-84992, 59-20696, 59-33176, 60-11389, 61-58788, 61-252189, etc., and all of them are of the amine type, but cannot sufficiently satisfy both of water resistance and light resistance, although improved.
  • The recording medium of the present invention, which uses an aluminum type compound as different from the amine type as in the prior art as the dye fixing agent, has the effect of improving water resistance of the dye, and also has no deleterious effect on light resistance.
  • Further, although the polyaluminum compound can be used with an amine type dye fixing agent as described above mixed therein, the amine type water resistant agent in this case should be preferably within the range of 70% by weight or less, more preferably 25% by weight or less, of the polyaluminum compound. If it is contained in excess of 70%, the bad influence by use of the amine type water resistance-affording agent will appear to lower undesirably light resistance.
  • In the present invention, the ink receiving layer may also contain fluorescent brighteners, surfactants, defoaming agents, pH controllers, antifungal agents, UV-absorbers, antioxidants, etc., if necessary.
  • By use of the ink jet recording system for the recording medium of the present invention with a constitution as described above, for example, according to the recording method of the present invention which performs recording with a multi-colr aqueous ink such as yellow (Y), magenta (M), cyan (C), black (Bk), etc., no in-room decoloration occurs on the image obtained to give a recorded image with excellent storability.
  • The method of the present invention is a recording method by use of the recording medium of the present invention as described above, and the ink itself which is imparted by the ink jet recording method to the specific recording medium as described above in the recording method may be also known. For example, its recording agent may be water soluble dyes as represented by direct dyes, acidic dyes, basic dyes, reactive dyes, dyes for foods, etc. Preferable examples of the dyes particularly suitable for the ink in the ink jet recording system, which can give images satisfying requisite performances in combination with the above recording medium such as color forming characteristic, sharpness, stability, light resistance and others may include:
    Direct dyes such as
    C.I. Direct Black 17, 19, 32, 51, 71, 108, 146,
    C.I. Direct Blue 6, 22, 25, 71, 86, 90, 106, 199,
    C.I. Direct Red 1, 4, 17, 28, 83,
    C.I. Direct Yellow 12, 24, 26, 86, 98, 142,
    C.I. Direct Orange 34, 39, 44, 46, 60,
    C.I. Direct Violet 47, 48,
    C.I. Direct Brown 109,
    C.I. Direct Green 59, etc.;
    Acidic dyes such as
    C.I. Acid Black 2, 7, 24, 26, 31, 52, 63, 112, 118,
    C.I. Acid Blue 9, 22, 40, 59, 93, 102, 104, 113, 117, 120, 167, 229, 234,
    C.I. Acid Red 1, 6, 32, 37, 51, 52, 80, 85, 87, 92, 94, 115, 180, 256, 317, 315,
    C.I. Acid Yellow 11, 17, 23, 25, 29, 42, 61, 71,
    C.I. Acid Orange 7, 19,
    C.I. Acid Violet 49, etc.;
    and, otherwise,
    C.I. Basic Black 2,
    C.I. Basic Blue 1, 3, 5, 7, 9, 24, 25, 26, 28, 29,
    C.I. Basic Red 1, 2, 9, 12, 13, 14, 37,
    C.I. Basic Violet 7, 14, 27,
    C.I. Food Black 1, 2, etc.
    can be also used.
  • The above examples of dyes set forth above are particularly preferred for the ink applicable to the recording method of the present invention, and the dyes for the ink to be used in the present invention are not limited to these dyes.
  • Such water soluble dyes are used generally in the ink of the prior art at a ratio about 0.1 to 20% by weight of the ink, and the same ratio may be used also in the present invention.
  • The solvent to be used for the aqueous ink to be used in the present invention is water or a solvent mixture of water with a water soluble organic solvent, particularly preferably a solvent mixture of water and a water soluble organic solvent. As the water soluble organic solvent, one containing a polyhydric alcohol having drying prevention effect on ink is preferred. As the water, it is preferable to use deionized water instead of water in general containing various ions.
  • The content of the water soluble organic solvent in the ink may be generally within the range of from 0 to 95% by weight, preferably from 2 to 80% by weight, more preferably from 5 to 50% by weight.
  • A preferable water content may be 20 to 98%, more preferably 50 to 90%, based on the total weight of the ink.
  • The ink to be used in the present invention can also include surfactants, viscosity controllers, surface tension controllers, etc., if desired, in addition to the above components.
  • The method of performing recording by imparting the above ink to the above recording medium in the method of the present invention may be any recording method, but preferably the ink jet recording method, and said method may be any system, provided that it is a system capable of eliminating effectively the ink from the nozzle and imparting the ink to the recording medium which is the target of injection.
  • Particularly, the ink jet system which discharges ink through nozzle by the acting force due to the state change by the abrupt volume change of ink having received the action of heat energy according to the method disclosed in Japanese Laid-open Patent Publication No. 54-59936 can be effectively used.
  • The recording medium of the present invention as described above is suitable as the recording medium for ink jet recording, particularly by use of aqueous ink, and exhibits the following effects.
    • (1) Since it is highly absorptive of aqueous ink, it becomes substantially the same state as dried immediately after imparting of ink, and a part of the recording device, hands or fingers when contacted with the medium will not be contaminated, or the recorded image will not be contaminated.
    • (2) When used for ink jet recording, in addition to the above effect (1), the dot has high density with a shape approximate to true sphere, without excessive blurring of dot or occurrence of feathering from dot, whereby a sharp image with high resolution can be formed.
    • (3) Since it has excellent color characteristics, it is suitable for color printer.
    • (4) There is little problem of image storability inherent in coated paper and, in the ink jet recording method by use of the recording medium of the present invention and a multi-color ink, there occurs no problem of in-room decoloration which has occurred when the image obtained is stored on the wall or in the drawer in an office where no direct sunlight is irradiated for one to several months.
    • (5) The recording medium of the present invention, while possessing the above characteristics (1) to (4), is also excellent in water resistance and light resistance of the recorded image.
  • The present invention is described in more detail below by referring to Examples and Comparative examples, in which parts and % are based on weight unless otherwise noted.
  • Examples 1 to 4
  • By use of a substrate having a Stockigt sizing degree of 5 sec., a basis weight of 66 g/m² and containig calcium carbonate in an amount of 9.0% (5.9 g/m²) as calculated on ash content according to JIS-P-­8128, a coating solution having the composition shown below was coated according to the bar coater method to a coated amount on drying of 5 g/m² and dried at 110 °C for 3 minutes to obtain a recording medium of the present invention.
  • Coating solution composition
  • Pigment 24 parts
    Polyvinyl alcohol (PVA-117, produced by Kuraray) 8 parts
    Polyvinyl alcohol (PVA-117, produced by Kuraray) 8 parts
    Water 200 parts
  • The pigments used are shown below in Table 1.
  • Comparative example 1
  • A recording medium was prepared in the same manner as in Example 1 except for using a paper for PPC having a Stöckigt sizing degree of 24 sec. and a basis weight of 66 g/m² (paper for Canon NP dry) as the base paper.
  • Examples 5 to 8 and Comparative examples 2 and 3
  • By use of a paper having a Stockigt sizing degree of 0 sec., a basis weight of 65 g/m² and calcium carbonate in an amount of 2.4% (1.6 g/m²) as calculated on ash content as the base paper, a coating solution with the same composition as in Example 1 was coated by the bar coating method to a coated amount on drying of 7 g/m² and dried at 110 °C to obtain the recording media of the present invention and Comparative example.
  • As the pigments, the mixtures of alumina with other pigments as shown in Table 2 were used.
    Figure imgb0001
    Figure imgb0002
    Table 2
    I II III IV
    Example 5 24 parts 0 parts 4.8 (g/m²) 1 (sec)
    Example 6 20 4 4.8 1
    Comparative example 2 0 24 4.5 1
    Remarks
    I .... Alumina (AKP-G, Sumitomo Kagaku)
    II .... Zinc oxide (active zinc white AZO, produced by Seido Kagaku, Particle size 0.8 µm, specific surface area 64 m²/g)
    III ... Amount of pigment coated (g/m²)
    IV .... Sizing degree of recording medium (sec)
    I II III IV
    Example 7 24 parts 0 parts 4.6 (g/m²) 2 (sec)
    Example 8 20 4 4.6 2
    Comparative example 3 0 24 4.8 1
    Remarks
    I .... Aerosil aluminum oxide-C (Degussa)
    II .... Finesil X-37 (Tokuyama soda, Particle size 2.7 µm, Specific surface area 260 m²/g)
    III ... Amount of pigment coated (g/m²)
    IV .... Sizing degree of recording medium (sec)
  • The ink jet recording adaptability of the above recording medium was evaluated by performing the ink jet recording with an ink having the composition shown below by means of an ink jet printer having ink jet heads equipped with 128 nozzles with nozzle interval of 1 mm/16 nozzles corresponding to the four colors of Y, M, C and Bk.
    Ink Composition
    Dye 5 parts
    Diethylene glycol 20 parts
    Water 78 parts
    Dye
    Y: C.I. Direct Yellow 86
    M: C.I. Acid Red 35
    C: C.I. Direct Blue 199
    Bk: C.I. Food Black 2
  • Evaluation was conducted for the items shown below. The results are shown below in Table 3.
    • (1) Ink absorptivity was evaluated by means of the ink jet printer as described above. Sharp printed image without color mixing at the printing boundary between the printed letters printed with the respective colors of Y, M, C and Bk was evaluated as O, and one which is not so as X.
    • (2) For image density, the image density of a printed matter (BK) of solid printing by means of the same ink jet printer was evaluated by use of a Macbeth reflection densitometer RD-918.
    • (3) Storability in room was measured by leaving the printed matter used in the above (2) (Bk) plastered on the wall in an office to stand for 6 months. The difference ΔE*ab between the chromacity of the image immediately after printing (before standing) and the chromaticity of the image after standing was determined for evaluation of storability in room.
    • (4) For paper powder, when the ink receiving layer surface is scratched with a pencil with a hardness of H, one with much generation of paper powder by peel-off or cutting of the coated layer is evaluated as x, and good one as O.
    Table 3
    Ink Absorptivity Image Density In-room storability (ΔE*ab) Paper Powder
    Example 1 1.65 4.5
    Example 2 1.48 2.5
    Example 3 1.36 9.4
    Example 4 1.56 11.9
    Comparative Example 1 × 1.30 5.6
    Example 5 1.58 5.2
    Example 6 1.48 4.6
    Comparative Example 2 × 1.16 2.1
    Example 7 1.42 3.2
    Example 8 1.47 6.8
    Comparative Example 3 1.57 25.4
    Examples 9 to 11 and Comparative examples 4 and 5
  • By use of a usual paper of fine quality (Ginkan, trade name, manufactured by Sanyo Kokusaku Pulp) as the substrate, it was coated with a coating solution I shown below to a coated amount on driving of 20 g/m² by the bar coated method and dried at 110 °C for 5 minutes to form an ink holding layer, and on the ink holding layer was coated a coating solution II shown below to a coated amount on drying of 7 g/m² by the bar coater method, followed by drying at 110 °C for 3 minutes, to form a surface layer to prepare recording media of the present invention and Comparative example.
  • Composition of coating solution I
  • Synthetic silica (spherical silica, BET specific surface area 700m²/g, average particle size 20µm, produced by Asahi Glass)
    18 parts
    Polyvinyl alcohol (PVA-117/R-1130, produced Kuraray) 6 parts
    Water 76 parts
  • Composition of coating solution II Example 9
  • Porous alumina (RG-40, produced by Iwatani Kagaku Kogyo specific surface area 48m²/g) 13 parts
    Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts
    Water 77 parts
  • Example 10
  • Fine particulate alumina (Aerosil, aluminum oxide-C, produced by Nihon Aerosil, BET specific surface area 100m²/g) 13 parts
    Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts
    Water 77 parts
  • Example 11
  • High purity alumina (AKP-G, produced by Sumitomo Kagaku, BET specific surface area 130m²/g) 13 parts
    Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts
    Water 77 parts
  • Comparative example 4
  • Fine powder silica (Syloid 74, produced by Fujidevison, BET specific surface area 300m²/g) 13 parts
    Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts
    Water 77 parts
  • Comparative example 5
  • Zinc oxide (active zinc white AZO, produced by Seido Kagaku BET specific surface area 64m²/g) 13 parts
    Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts
    Water 77 parts
  • Example 12
  • On the same base paper as in Example 9, by use of a coating solution III shown below, it was coated by the bar coater method to a coated amount on drying of 20 g/m², followed by drying at 110 °C for 5 minutes, to form an ink holding layer, and on the ink holding layer was coated a coating solution IV shown below to a coated amount on drying of 7 g/m², followed by drying at 110 °C for 3 minutes to form a surface layer, thus providing a recording medium of the present invention.
  • Composition of coating solution III
  • Synthetic silica(Syloid 620, BET specific surface area 300m²/g average particle size 12µm, produced by Fujidevison) 20 parts
    Polyvinyl alcohol (PVA-117, produced by Kuraray) 5 parts
    Water 75 parts
  • Composition of coating solution IV
  • γ-alumina (UA-5605, produced by Showa Denko, BET specific surface area 64m²/g) 12 parts
    Polyvinyl alcohol (PVA-110, produced by Kuraray) 11 parts
    Water 77 parts
  • Comparative example 6
  • On the same base paper as used in Example 10 was coated a coating solution shown below by the bar coated method to a coated amount of 15 g/m², followed by drying at 140 °C for 5 minutes to form a lower layer with low ink absorptivity. On the lower layer was applied coating by use of the coating solution used in Example 10 in the same manner as in Example 10, followed by drying, to obtain a recording medium 6 for comparison.
  • Composition of coating solution
  • Polyvinyl pyrrolidone (PVP K-90, produced by GAF) 9 parts
    Isobutylene/Maleic anhydride copolymer (Isovan 10, produced by Kuraray Isoprene Chemical) 3 parts
    Dimethyl formamide 88 parts
  • The evaluation for the respective recording media of the above Examples 9 to 12 and Comparative examples 4 to 6 was conducted for the following items. The results are shown below in Table 4.
    • (1) Ink absorptivity was evaluated by means of the above ink jet printer. The recorded image with excessive line boldness at the mixed color portion of two colors than at the single color portion and generation of ink flow-out is evaluated as x, one without line boldness as ○, one with slight generation as Δ. Further, one without line boldness even at the overlapped portion of three colors as ⓞ.
    • (2) Storability in room is measured by printing a solid pattern of Bk by use of the above printer, and leaving the printed product to stand for six months as plastered on the wall in an office. The difference between the chromaticity of the image and the chromaticity of the image immediately after printing (ΔE*ab) is determined for evaluation of decoloration in room.
    • (3) For the color characteristic, the chromacity of the printed products by solid printing (Y,M,C) by use of the above printer was measured by use of a high speed color analyzer (produced by Murakami Shikisai Kagaku).
    • (4) For the image density, O.D. of the printed product by solid printing (Bk) by use of the above printer was measured by use of Macbeth densitometer RD-­914.
    Table 4
    I II III IV
    Y M C
    Example 9 7.3 77.8 67.9 50.0 1.26
    Example 10 13.3 83.3 71.9 53.2 1.55
    Example 11 14.5 82.4 72.2 54.1 1.66
    Example 12 8.6 78.1 69.2 50.8 1.37
    Comparative Example 4 34.8 82.3 72.0 52.1 1.63
    Comparative Example 5 5.4 61.9 53.7 46.3 1.18
    Comparative Example 6 × 9.4 83.4 72.1 53.5 1.42
    Note:
    I: Ink absorptivity
    II: In-room storability (ΔE*ab)
    III: Color characteristic
    IV: Image density (Bk)
    Examples 13 - 16 and Comparative examples 7 - 9
  • Except for using the coating compositions shown below (Table 5), recording media were prepared in the same manner as in Example 1.
  • Composition of coating solution
  • Pigment 20 parts
    Polyvinyl alcohol (PVA-110, produced by Kuraray) 10 parts
    Water-resistant agent 3.6 parts
    Water 266 parts
    Figure imgb0003
  • By use of the above recording media, recording was performed evaluated in the same manner as in Example 1. The results are shown in Table 6.
  • Water resistance and light resistance were evaluated as described below.
  • Water resistance was evaluated by dipping the printed product of (1) in running water (20 °C) for 5 minutes, and determining the ratio of the image density at the M printed portion after dipping relative to the image density before dipping (residual O.D. ratio).
  • Light resistance was evaluated by irradiating the printed product of (1) by use of Xenon Fade-Ometer (manufactured by Ci-35 Atlas Co.) under the conditions of a black panel temperature of 63 °C and a humidity of 70% RH for 100 hours, and determining the ratio of the image density at the M printed portion after irradiation relative to the image density before irradiation. Table 6
    Ink absorptivity Image density Water resistance Light resistance In-room storability (ΔE*ab)
    Example 13 o 1.60 95% 83% 3.4
    14 o 1.48 94% 78% 2.3
    15 o 1.59 98% 80% 3.2
    16 o 1.48 99% 74% 2.1
    Reference Example 1 o 1.62 72% 88% 4.4
    Comparative Example 7 o 1.63 80% 76% 26.3
    8 o 1.59 102% 43% 3.1
    9 o 1.48 99% 38% 1.9

Claims (32)

1. A recording medium, comprising a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity.
2. A recording medium according to Claim 1, wherein the aluminum oxide particles have a BET surface area within the range of from 60 to 170 m²/g.
3. A recording medium according to Claim 1, wherein the aluminum oxide particles have an average particle size of 5 µm or less.
4. A recording medium according to Claim 1, wherein the aluminum oxide particles have an average particle size of 1 µm or less.
5. A recording medium according to Claim 1, wherein the aluminum oxide particles comprise 80% by weight of all the pigments in the surface layer.
6. A recording medium according to Claim 1, wherein the amount of the surface layer coated is within the range of from 0.3 to 9 g/m².
7. A recording medium according to Claim 1, wherein the lower layer is a paper having a Stöckigt sizing degree according to JIS-P-8122 of 0 to 15 sec.
8. A recording medium according to Claim 1, wherein the lower layer is a layer composed mainly of a pigment.
9. A recording medium, comprising a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity, and having a Stöckigt sizing degree according to JIS-P-8122 of 0 to 15 sec.
10. A recording medium according to Claim 9, wherein the aluminum oxide particles have a BET surface area within the range of from 60 to 170 m²/g.
11. A recording medium according to Claim 9, wherein the aluminum oxide particles have an average particle size of 5 µm or less.
12. A recording medium according to Claim 9, wherein the aluminum oxide particles have an average particle size of 1 µm or less.
13. A recording medium according to Claim 9, wherein the aluminum oxide particles comprise 80% by weight of all the pigments in the surface layer.
14. A recording medium according to Claim 9, wherein the amount of the surface layer coated is within the range of from 0.3 to 9 g/m².
15. A recording medium according to Claim 9, wherein the lower layer is a paper having a Stöckigt sizing degree according to JIS-P-8122 of 0 to 15 sec.
16. A recording medium according to Claim 9, wherein the lower layer is a layer composed mainly of a pigment.
17. An ink jet recording method which performs recording by imparting small droplets of an aqueous ink to a recording medium, wherein said aqueous ink contains an acidic dye and/or a direct dye, and said recording medium comprises a surface layer composed mainly of aluminum oxide particles and a lower layer having ink absorptivity.
18. An ink jet recording method according to Claim 17, wherein said small droplets of the ink are formed by permitting heat energy to act on the ink.
19. A recording medium, comprising a surface layer composed mainly of aluminum oxide particles containing polyaluminum hydroxide and/or polyaluminum chloride and a lower layer having ink absorptivity.
20. A recording medium according to Claim 19, wherein the aluminum oxide particles have a BET surface area within the range of from 60 to 170 m²/g.
21. A recording medium according to Claim 19, wherein the aluminum oxide particles have an average particle size of 5 µm or less.
22. A recording medium according to Claim 19, wherein the aluminum oxide particles have an average particle size of 1 µm or less.
23. A recording medium according to Claim 19, wherein the aluminum oxide particles comprise 80% by weight of all the pigments in the surface layer.
24. A recording medium according to Claim 19, wherein the amount of the surface layer coated is within the range of from 0.3 to 9 g/m².
25. A recording medium according to Claim 19, wherein the lower layer is a paper having a Stöckigt sizing degree according to JIS-P-8122 of 0 to 15 sec.
26. A recording medium according to Claim 19, wherein said polyaluminum hydroxide and/or polyaluminum chloride is contained in an amount within the range of from 0.01 to 5 g/m².
27. A recording medium, comprising a surface layer composed mainly of aluminum oxide particles having particle sizes of 5 µm or less provided on a liquid absorptive base paper.
28. A recording medium according to Clam 27, having a Stöckigt sizing degree of 0 to 15 sec.
29. A recording medium according to Claim 27, wherein said aluminum oxide particles have particle sizes of 1 µm or less.
30. A recording medium according to Claim 27, wherein the aluminum oxide particles comprises 80% by weight of all the pigments in the surface layer.
31. A recording medium according to Claim 27, wherein the amount of the surface layer coated is within the range of from 0.3 to 7 g/m².
32. A recording medium according to Claim 27, wherein said aluminum oxide particles have a BET surface area within the range of from 60 to 170 m²/g.
EP89103526A 1988-03-04 1989-02-28 Recording medium and ink jet recording method by use thereof Expired - Lifetime EP0331125B1 (en)

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
JP49676/88 1988-03-04
JP4967688 1988-03-04
JP11060588 1988-05-09
JP110605/88 1988-05-09
JP1014042A JP2694771B2 (en) 1988-03-04 1989-01-25 Recording medium and recording method using the same
JP14042/89 1989-01-25
JP1018004A JPH02198889A (en) 1989-01-27 1989-01-27 Material to be recorded and ink-jet recording method using said material
JP18004/89 1989-01-27

Publications (3)

Publication Number Publication Date
EP0331125A2 true EP0331125A2 (en) 1989-09-06
EP0331125A3 EP0331125A3 (en) 1990-09-05
EP0331125B1 EP0331125B1 (en) 1994-09-21

Family

ID=27456129

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89103526A Expired - Lifetime EP0331125B1 (en) 1988-03-04 1989-02-28 Recording medium and ink jet recording method by use thereof

Country Status (9)

Country Link
EP (1) EP0331125B1 (en)
AT (1) ATE111818T1 (en)
AU (1) AU626290B2 (en)
CA (1) CA1337388C (en)
DE (1) DE68918307T2 (en)
DK (1) DK172062B1 (en)
ES (1) ES2059591T3 (en)
FI (1) FI97345C (en)
NO (1) NO301410B1 (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0391308A1 (en) * 1989-04-03 1990-10-10 Canon Kabushiki Kaisha Recording medium and recording method using the same
EP0450540A1 (en) * 1990-04-02 1991-10-09 Canon Kabushiki Kaisha Ink-jet recording medium and ink-jet recording method making use of it
EP0709223A1 (en) * 1994-10-27 1996-05-01 Canon Kabushiki Kaisha Recording medium, and image forming method and printed material making use of the same
EP0806299A2 (en) * 1996-05-09 1997-11-12 Felix Schoeller jr Foto- und Spezialpapiere GmbH & Co. KG Recording material for the ink jet printing process
US6000794A (en) * 1994-10-27 1999-12-14 Canon Kabushiki Kaisha Image forming method
WO2000078552A1 (en) * 1999-06-22 2000-12-28 Rhodia Chimie Ink jet recording medium
EP1114735A2 (en) * 2000-01-06 2001-07-11 Westvaco Corporation Glossy inkjet coated paper and process of making it
EP1193077A2 (en) * 2000-09-27 2002-04-03 Canon Kabushiki Kaisha Recording medium and image forming method utilizing the same
CN1083914C (en) * 1997-09-24 2002-05-01 可乐丽股份有限公司 Leather-like sheet
EP1329330A1 (en) 2000-10-24 2003-07-23 Mitsubishi Paper Mills Limited Recording material for ink-jet
FR2876384A1 (en) * 2004-10-13 2006-04-14 Honnorat Rech S & Services Sar LIQUID COMPOSITION FOR PROCESSING MEDIA

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60232990A (en) * 1984-05-02 1985-11-19 Mitsubishi Paper Mills Ltd Ink jet recording medium
JPS61280983A (en) * 1985-06-07 1986-12-11 Teijin Ltd Recording sheet
EP0275711A1 (en) * 1986-12-29 1988-07-27 Canon Kabushiki Kaisha Recording medium and ink jet recording method by use thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60232990A (en) * 1984-05-02 1985-11-19 Mitsubishi Paper Mills Ltd Ink jet recording medium
JPS61280983A (en) * 1985-06-07 1986-12-11 Teijin Ltd Recording sheet
EP0275711A1 (en) * 1986-12-29 1988-07-27 Canon Kabushiki Kaisha Recording medium and ink jet recording method by use thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
ABSTRACT BULLETIN OF THE INSTITUTE OF PAPER CHEMISTRY, vol. 57, no. 4, October 1986, page 600, abstract 5349, Appleton, Wisconsin, US; & JP-A-60 232 990 (MITSUBISHI PAPER MILLS LTD) 19-11-1985 *
PATENT ABSTRACTS OF JAPAN, vol. 11, no. 146 (M-587)[2593], 13th May 1987; & JP-A-61 280 983 (TEIJIN LTD) 11-12-1986 *

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0391308A1 (en) * 1989-04-03 1990-10-10 Canon Kabushiki Kaisha Recording medium and recording method using the same
US5182175A (en) * 1989-04-03 1993-01-26 Canon Kabushiki Kaisha Recording medium
US5907342A (en) * 1989-04-03 1999-05-25 Canon Kabushiki Kaisha Recording method using recording medium
EP0450540A1 (en) * 1990-04-02 1991-10-09 Canon Kabushiki Kaisha Ink-jet recording medium and ink-jet recording method making use of it
US5171626A (en) * 1990-04-02 1992-12-15 Canon Kabushiki Kaisha Ink-jet recording medium and ink-jet recording method making use of it
EP0709223A1 (en) * 1994-10-27 1996-05-01 Canon Kabushiki Kaisha Recording medium, and image forming method and printed material making use of the same
US5679451A (en) * 1994-10-27 1997-10-21 Canon Kabushiki Kaisha Recording medium
US6000794A (en) * 1994-10-27 1999-12-14 Canon Kabushiki Kaisha Image forming method
EP0806299A2 (en) * 1996-05-09 1997-11-12 Felix Schoeller jr Foto- und Spezialpapiere GmbH & Co. KG Recording material for the ink jet printing process
EP0806299A3 (en) * 1996-05-09 1998-04-08 Felix Schoeller jr Foto- und Spezialpapiere GmbH & Co. KG Recording material for the ink jet printing process
US5911855A (en) * 1996-05-09 1999-06-15 Felix Schoeller Jr. Foto-Und Spezialpapeire Gmbh & Co. Kg Printing material for ink-jet printing methods
CN1083914C (en) * 1997-09-24 2002-05-01 可乐丽股份有限公司 Leather-like sheet
FR2795366A1 (en) * 1999-06-22 2000-12-29 Rhodia Chimie Sa Ink jet recording medium comprises polymeric film or cellulose or cardboard substrate and ink receiving layer, consisting of at least two separate sublayers fixed onto substrate
WO2000078552A1 (en) * 1999-06-22 2000-12-28 Rhodia Chimie Ink jet recording medium
EP1114735A2 (en) * 2000-01-06 2001-07-11 Westvaco Corporation Glossy inkjet coated paper and process of making it
EP1114735A3 (en) * 2000-01-06 2001-09-12 Westvaco Corporation Glossy inkjet coated paper and process of making it
EP1193077A2 (en) * 2000-09-27 2002-04-03 Canon Kabushiki Kaisha Recording medium and image forming method utilizing the same
EP1193077A3 (en) * 2000-09-27 2002-07-03 Canon Kabushiki Kaisha Recording medium and image forming method utilizing the same
US6696118B2 (en) 2000-09-27 2004-02-24 Canon Kabushiki Kaisha Recording medium and image forming method utilizing the same
EP1329330A1 (en) 2000-10-24 2003-07-23 Mitsubishi Paper Mills Limited Recording material for ink-jet
EP1329330B2 (en) 2000-10-24 2012-12-26 Mitsubishi Paper Mills Limited Recording material for ink-jet
FR2876384A1 (en) * 2004-10-13 2006-04-14 Honnorat Rech S & Services Sar LIQUID COMPOSITION FOR PROCESSING MEDIA
WO2006040460A2 (en) * 2004-10-13 2006-04-20 Honnorat Recherches & Services Liquid composition for treating supports
WO2006040460A3 (en) * 2004-10-13 2007-04-05 Honnorat Rech S & Services Liquid composition for treating supports

Also Published As

Publication number Publication date
NO890925L (en) 1989-09-05
DK103789D0 (en) 1989-03-03
DE68918307T2 (en) 1995-05-18
AU626290B2 (en) 1992-07-30
FI97345C (en) 1996-12-10
AU3098789A (en) 1989-09-07
ES2059591T3 (en) 1994-11-16
NO301410B1 (en) 1997-10-27
DK172062B1 (en) 1997-10-06
CA1337388C (en) 1995-10-24
DE68918307D1 (en) 1994-10-27
EP0331125A3 (en) 1990-09-05
EP0331125B1 (en) 1994-09-21
ATE111818T1 (en) 1994-10-15
NO890925D0 (en) 1989-03-03
FI891040A (en) 1989-09-05
DK103789A (en) 1989-09-05
FI891040A0 (en) 1989-03-03
FI97345B (en) 1996-08-30

Similar Documents

Publication Publication Date Title
US5266383A (en) Recording medium and ink jet recording method by use thereof
EP0411638B1 (en) Recording medium and method of recording using the same
EP0450540B1 (en) Ink-jet recording medium and ink-jet recording method making use of it
US5907342A (en) Recording method using recording medium
EP0943450B1 (en) Recording sheet for ink jet printer
EP1038691B1 (en) A process for producing an ink jet recording material
EP0405417B1 (en) Recording medium and process for recording using the same
GB2129333A (en) Recording medium
US6565950B1 (en) Recording medium, image forming method utilizing the same, method for producing the same, alumina dispersion and method for producing the same
EP1174279B1 (en) Ink-jet recording material containing ultraviolet ray-absorber
EP1122084B1 (en) Ink-jet recording material suitable for pigment ink
KR20060042134A (en) Ink jet recording sheet
US20050186365A1 (en) Ink-jet recording sheet, method for making the same, and image-forming method
EP1655142B1 (en) Ink-jet recording material and method for preparing the same
EP0331125B1 (en) Recording medium and ink jet recording method by use thereof
JPS6157380A (en) Ink jet recording medium
JP2627447B2 (en) Water resistant inkjet recording sheet
JPH0717090B2 (en) Inkjet recording medium
CA1337321C (en) Recording medium and ink jet recording method
JP2694771B2 (en) Recording medium and recording method using the same
US6443570B1 (en) Ink jet printing method
EP1288011B1 (en) Ink jet recording element and printing method
JPH01283182A (en) Ink jet recording method
JP2621096B2 (en) recoding media
JPH06143793A (en) Ink-jet recording sheet and recording thereof

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH DE ES FR GB IT LI NL SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH DE ES FR GB IT LI NL SE

17P Request for examination filed

Effective date: 19910102

17Q First examination report despatched

Effective date: 19921207

ITTA It: last paid annual fee
GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE ES FR GB IT LI NL SE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Effective date: 19940921

Ref country code: BE

Effective date: 19940921

REF Corresponds to:

Ref document number: 111818

Country of ref document: AT

Date of ref document: 19941015

Kind code of ref document: T

REF Corresponds to:

Ref document number: 68918307

Country of ref document: DE

Date of ref document: 19941027

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2059591

Country of ref document: ES

Kind code of ref document: T3

ET Fr: translation filed
ITF It: translation for a ep patent filed
EAL Se: european patent in force in sweden

Ref document number: 89103526.3

REG Reference to a national code

Ref country code: CH

Ref legal event code: PK

RIN2 Information on inventor provided after grant (corrected)

Free format text: SAKAKI, MAMORU * SHIMOMURA, MASAKO * MUNAKATA, MEGUMI * NAKATSUGAWA, TOMOMI * SATO, HOROSHI

NLXE Nl: other communications concerning ep-patents (part 3 heading xe)

Free format text: PAT.BUL.03/95 SHOULD BE ADDED:SATO, HOROSHI TE YOKOHAMA,JAPAN (SEE EUROPEAN PATENT BULLETIN 150295/07)

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20060207

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20060215

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 20060301

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20060302

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20070222

Year of fee payment: 19

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20070228

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20070228

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20070228

Year of fee payment: 19

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20070301

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20070901

EUG Se: european patent has lapsed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20070622

Year of fee payment: 19

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20070901

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20070208

Year of fee payment: 19

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20070301

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20070301

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20080228

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20081031

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20080902

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20080229

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20080228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20080228