EP1008457B1 - Ink-jet recording sheet with image-protecting layer - Google Patents

Ink-jet recording sheet with image-protecting layer Download PDF

Info

Publication number
EP1008457B1
EP1008457B1 EP99309809A EP99309809A EP1008457B1 EP 1008457 B1 EP1008457 B1 EP 1008457B1 EP 99309809 A EP99309809 A EP 99309809A EP 99309809 A EP99309809 A EP 99309809A EP 1008457 B1 EP1008457 B1 EP 1008457B1
Authority
EP
European Patent Office
Prior art keywords
ink
jet recording
recording sheet
ink jet
layer
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.)
Expired - Lifetime
Application number
EP99309809A
Other languages
German (de)
French (fr)
Other versions
EP1008457A1 (en
Inventor
Takashi Nippon paper Industries Co. Ltd. Ueno
Noboru Nippon Paper Industries Co. Ltd. Kondo
Akinobu Nippon Paper Ind. Co. Ltd. Chatani
Yoshihiro Nippon Paper Ind. Co. Ltd. Kuroyama
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.)
Nippon Paper Industries Co Ltd
Jujo Paper Co Ltd
Original Assignee
Nippon Paper Industries Co Ltd
Jujo Paper Co Ltd
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 JP10343037A external-priority patent/JP2000169873A/en
Priority claimed from JP05060899A external-priority patent/JP3300680B2/en
Priority claimed from JP06855399A external-priority patent/JP3377464B2/en
Application filed by Nippon Paper Industries Co Ltd, Jujo Paper Co Ltd filed Critical Nippon Paper Industries Co Ltd
Publication of EP1008457A1 publication Critical patent/EP1008457A1/en
Application granted granted Critical
Publication of EP1008457B1 publication Critical patent/EP1008457B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/02Mixtures of base-materials and thickeners
    • 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • 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
    • 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
    • B41M5/5227Macromolecular coatings characterised by organic non-macromolecular additives, e.g. UV-absorbers, plasticisers, surfactants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/061Carbides; Hydrides; Nitrides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/061Carbides; Hydrides; Nitrides
    • C10M2201/0613Carbides; Hydrides; Nitrides used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/087Boron oxides, acids or salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/10Compounds containing silicon
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/0405Siloxanes with specific structure used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/06Groups 3 or 13
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/04Molecular weight; Molecular weight distribution
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/055Particles related characteristics
    • C10N2020/06Particles of special shape or size
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • the present invention relates to a recording material that can be print on with ink containing water-soluble dye.
  • the present invention relates to an ink jet recording sheet which provides a superior combination of ink absorbency, ink coloration, resistance of the recorded image to light, resistance of the recorded image to water and surface gloss.
  • Ink jet recording is a method by which fine ink drops are jetted out using any kind of jetting method to form an image on a recording material. Since this method enables a recording apparatus to be operated at a high speed and the apparatus is generally inexpensive, the use of ink jet recording systems has been spreading rapidly. Moreover, the use of multicolor ink jet recording methods enables the formation of color images comparable to silver-salt films with high resolution and high quality. Digital images, for example those obtained by a digital camera, are increasingly printed with an ink jet printer. The recorded materials are more often being displayed or stored for considerably long period because of the high image quality. Therefore, it is desirable that the ink jet recording materials have good preservation characteristics, especially good light resistance, as well as high image quality.
  • a process to add UV absorber such as benzophenones and benzotriazoles Japanese Tokkai Sho 63-222885, "Tokkai” means an "unexamined published patent application”
  • a process to add antioxidant such as hindered amines
  • a process to add zinc oxide and cationic resins concurrently Japanese Tokkai Hei 7-32725
  • these additives are difficult to disperse evenly in the materials, these attempts did not provide a satisfactory improvement.
  • the objective of this invention is to provide a recording material that can be recorded by ink with water-soluble dye, particularly to provide an ink jet recording sheet, which is superior in ink absorbency, ink coloration, light resistance, water resistance and surface gloss.
  • One subject of the present invention is an ink jet recording sheet having on an ink-receiving support an image preserving layer comprising anionic colloidal silica and zinc oxide particulates with an average particle size of about 15 to 380 nm and having a 75 degree specular glossiness of at least about 25% at the surface.
  • Another subject of the present invention is an ink jet recording sheet having on an ink-receiving support, in succession, an image preserving layer comprising an anionic colloidal silica and zinc oxide particulates with an average particle size of about 15 to 380 nm and a fixing layer comprising a cationic colloidal silica and a cationic polymer electrolyte.
  • the support used in the present invention may be any of known supports capable of absorbing an ink containing a water-soluble dye, is preferably a support having an ink-receiving layer comprising a pigment and a binder on a base paper.
  • the image preserving layer formed on the ink-receiving layer mentioned before comprises zinc oxide particulates with an average particle size of about 15 to 380 nm, preferably about 20 to 300 nm, which absorbs UV light, and anionic colloidal silica, which is compatible with said particulates and can provide a glossy surface property in order to obtain compatibility between the light resistance and the high quality of recorded image.
  • Colloidal silica of this invention is the stabilized colloidal solution of silica to make its utilization easy, as described in Kagaku Binran (Chemical Reference Guide) published by Maruzen, Oct.15, 1986.
  • the average particle size of zinc oxide particulates is less than 15 nm, the image-preserving layer is very closely packed and therefore has a poor ink absorbency, which not only makes it difficult to obtain images of high quality but also causes problems in cost and operability.
  • the average particle size is larger than 380 nm, the transparency of the image-preserving layer becomes worse due to light scattering thereby reducing the recorded density.
  • the average particle size of zinc oxide particulates is measured by using a scanning electron microscope.
  • the colloidal silica which is necessary for glossy surface, needs to be anionic colloidal silica. Since the isoelectric point of anionic silica is usually around pH 2, the silica is negatively charged in the almost all range above pH 2, which is suitable for this invention. On the contrary, the colloidal silica that is reversely charged by having cations, for example, obtained by hydrolysis of metal salts, absorbed on the surface, has problems in operability due to poor compatibility with the zinc oxide particulates.
  • the configuration of the anionic colloidal silica is preferably non-spherical shape, in which several particulates interlink as in a shape of beads or a ring.
  • the coverage of the image-preserving layer be about 1 to 6 g/m 2 , preferably about 1.5 to 5 g/m 2 , on a dry solids basis.
  • the coverage of the image-preserving layer is less than 1 g/m 2 , sufficient light resistance and surface gloss cannot be attained.
  • the coverage is larger than 6 g/m 2 , the ink absorbency of the layer becomes poor and high quality images cannot be obtained.
  • the content of the zinc oxide particulates in the image-preserving layer is desired to be about 2 to 25 parts by weight, preferably about 3 to 20 parts by weight based on the 100 parts by weight of the anionic colloidal silica.
  • the content of the zinc oxide particulates is less than 2 parts by weight, sufficient light resistance cannot be attained.
  • the content is larger than 25 parts by weight, the recorded density and the surface gloss become poor and high quality images cannot be obtained.
  • the 75 degree specular glossiness of the image preserving layer needs to be at least about 25%, preferably at least about 30% at the surface, measured in accordance with JIS(Japanese Industrial Standards) P8142, in order to obtain sufficient reproducibility of image similar to a silver salt film.
  • the base paper used for an ink-receiving support of the present invention can be made from various types of paper pulps.
  • the pulp for paper include chemical pulp such as LBKP (hardwood bleached pulp) and NBKP (softwood bleached pulp), mechanical pulp such as GP(groundwood pulp) and TMP(thermo mechanical pulp), waste paper pulp and mixture thereof, but the pulp is not limited to those.
  • additives such as fillers, sizing agents and paper reinforcing agents
  • the additives are not limited to those and can be selected from known fillers and known additives as required.
  • Starch or other surface-sizing agents can be size pressed or coated.
  • antifoaming agents, pH regulators, pigments and coloring dyes for adjusting color, fluorescent pigments for improving visual whiteness and the like can be added as well.
  • the coverage of the ink-receiving layer formed on the base paper be about 5 to-25 g/m 2 , preferably about 7 to 20 g/m 2 , on a dry solids basis.
  • the coverage of the ink-receiving layer is less than 5 g/m 2 , the ink absorbency of the layer becomes poor which will cause bleeding of ink.
  • the coverage is larger than 25 g/m 2 , the amount of absorbed ink becomes excessive thereby reducing the recording density and this will also degrade the quality of image.
  • the ink-receiving layer comprises pigment and binder.
  • white pigment such as light and heavy calcium carbonate, kaolin, clay, talc, titanium dioxide, zinc oxide, satin white, magnesium silicate, calcium silicate, aluminum silicate, aluminum hydroxide, alumina, quasi-boehmite, synthetic amorphous silica, magnesium carbonate, zeolite.
  • synthetic amorphous silica is more preferred as a pigment for the ink-receiving layer because it provides a superior combination of ink coloration, ink absorbency and cost.
  • the binder resin used for the ink-receiving layer can be selected from any resins that can bond strongly to the base paper and can form films when coated and dried. It is desirable to use starches such as oxidized starch, esterified starch, enzyme-modified starch and cationic starch; polyvinyl alcohol with various degrees of saponification and derivatives thereof; casein, soy proteins; cellulose derivatives such as carboxymethyl cellulose and hydroxymethyl cellulose; styrene-acrylic resin; isobutylene-maleic anhydride resin; acrylic emulsion; vinyl acetate emulsion; vinylidene chloride emulsion; polyester emulsion; styrene-butadiene latex; acrylonitrile-butadiene latex and the like.
  • starches such as oxidized starch, esterified starch, enzyme-modified starch and cationic starch; polyvinyl alcohol with various degrees of saponification and derivatives thereof; casein, soy
  • a dye fixing agent that is cationic resin can be added to ink-receiving layer in order to impart water resistance property of the image.
  • examples of such agents include dicyandiamide-alkylamine polycondensed material, dicyanodiamide-formaldehyde polycondensed material, polyethylene-imine derivatives, alkylamine(-ammonium)-epichlorohydrin polycondensed material, polymethacrylic acid quaternary ammonium salt derivatives, polydiallyl-dimethyl-ammonium chloride, and other commercially available dye fixing agent. Mixtures of these can also be used without the loss of the advantage of the present invention.
  • the fixing layer of the present invention comprises cationic colloidal silica and cationic polymer electrolyte and provide a good combination of light resistance, water resistance and surface gloss. Further, it is preferred that the configuration of the cationic colloidal silica is non-spherical shape, in which several particulates interlink as in a shape of beads or a ring.
  • the fixing layer contains anionic colloidal silica or synthetic amorphous silica, problems are seen in operability due to the poor compatibility of the silica with the cationic polymer electrolyte.
  • the coverage of the fixing layer be about 1 to 6 g/m 2 , preferably about 1.5 to 5 g/m 2 , on a dry solids basis.
  • the coverage of the fixing layer is less than 1 g/m 2 , sufficient water resistance and surface gloss cannot be attained.
  • the coverage is larger than 6 g/m 2 , the ink absorbency of the layer-becomes poor and high quality images cannot be obtained.
  • the content of the cationic polymer electrolyte in the fixing layer is desired to be about 2 to 25 parts by weight, preferably about 3 to 20 parts by weight based on the 100 parts by weight of the cationic colloidal silica.
  • the content of the cationic polymer electrolyte is less than 2 parts by weight, the water resistance is sometimes insufficient.
  • the content is larger than 25 parts by weight, the ink absorbency and light resistance sometimes degrades.
  • the cationic polymer electrolyte of the present invention can be selected from dicyandiamide-alkylamine polycondensed material, dicyanodiamide-formaldehyde polycondensed material, polyethylene-imine derivatives, alkylamine (-ammonium)-epichlorohydrin polycondensed material, polymethacrylic acid quaternary ammonium salt derivatives, polydiallyl-dimethyl-ammonium chloride, other commercially available cationic polymer electrolyte and mixture thereof.
  • the fixing layer comprising cationic colloidal silica and cationic polymer electrolyte as a top layer, it becomes possible to obtain compatibility between water resistance and quality of recorded images.
  • the 75 degree specular glossiness is desirably at least about 30%, preferably at least about 35% at the surface of the fixing layer, measured in accordance with JIS(Japanese Industrial Standards) P8142.
  • the ink-receiving layer may comprise hindered amine compounds of amino ether type having alkoxyl groups in order to impart light resistance.
  • R 1 and R 2 of the formula (1) is preferably 6 to 10, and the alkyl group or carbonyl group of R 3 to R 6 is preferably a lower alkyl group with 1 to 4 carbons, more preferably methyl group.
  • the hindered amine compound of the amino ether type having alkoxyl groups is preferably bis-(2,2,6,-tetramethyl-1-(octyloxy)-4-piperidinyl)sebacate wherein R 1 is C 8 H 17 , R 2 is C 3 H 15 and R 3 to R 6 are methyl groups in the formula (1) (Tinuvin 123, manufactured by Ciba Specialty Chemicals, Inc.).
  • Hindered amine compounds generally generate nitroxy radicals by reacting with hydroperoxide or triplet oxygen in the air, which further react to form aminoethers by capturing polymer radicals generated by photodegradation of dyes contained in ink. Then the generated aminoethers react with peroxy radicals generated by a reaction between polymer radicals and oxygen in the air to regenerate nitroxy radicals. The aminoether also releases olefins, simultaneously generating hydroxylamine that react with the peroxy radicals to regenerate nitroxy radicals. This process is repeated to capture the radicals and hamper a chain reaction, thereby preventing the image from photodegrading.
  • the hindered amine compounds of the present invention have an amino ether as part of their chemical structure, it is considered that peroxy radicals are immediately captured when generated. Thus the hindered amine compound is very effective in preventing photodegradation of image. While in the case of conventional hindered amine compounds unsubstituted or substituted by alkyl or acetyl groups, it is considered that there is a large energy barrier to producing aminoethers, which inhibit the effective prevention of photodegradation.
  • the content of the hindered amine compounds in the ink-receiving layer is desired to be about 0.5 to 15 wt%, preferably about 2 to 8 wt%.
  • the content of the compounds is less than 0.5 wt%, the addition of the compounds would not be effective, and when the content is larger than 15 wt%, the applicability in manufacturing becomes worse.
  • the benzotriazole compounds of the present invention preferably include, for example, 2-(2-hydroxy-3,5-di-t-amylphenyl-2H-benzotriazole, iso-octyl-3,3-(2H-benzotriazole-2-yl)-5-t-butyl-4-hydroxyphenylpropionate, 2-[2-hydroxy-3,5-di(1,1-dimethylbenzyl)phenyl]-2H-benzotriazole, 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole, and the like.
  • the content of the benzotriazole compounds in the ink-receiving layer is desired to be about 0.5 to 12 wt%, preferably about 2.5 to 8 wt%.
  • the content of the benzotriazole compounds is less than 0.5 wt%, the addition of the compounds would not be effective, and when the content is larger than 12 wt%, it causes significant coloring in the applied layer.
  • the coating compositions for the ink-receiving layers, image-preserving layers and fixing layers may contain various additives, such as an antifoaming agent, a surface-sizing agent, a pH-adjusting agent, other CV absorber, an antioxidant, a dye or coloring pigment for adjusting color phase, a fluorescent dye and mixture thereof without the loss of the effect of the present invention.
  • various additives such as an antifoaming agent, a surface-sizing agent, a pH-adjusting agent, other CV absorber, an antioxidant, a dye or coloring pigment for adjusting color phase, a fluorescent dye and mixture thereof without the loss of the effect of the present invention.
  • the method of coating the ink-receiving layers, image-preserving layers and fixing layers on base paper includes conventional coaters of various kinds, e.g., a blade coater, an air knife coater, a roll coater, a curtain coater, a bar coater, a gate roll coater and a gravure coater and the like. Further various calendering treatments such as a machine calender, a soft calender, and a super calender can be used solely or in combination for finishing the surface.
  • the ink jet recording sheet of the present invention has on an ink-receiving support, in succession, an image preserving layer comprising zinc oxide particulates with a certain particular size to absorb UV light and anionic colloidal silica that is compatible with the particulates and a fixing layer comprising cationic colloidal silica to impart water resistance and surface gloss. Therefore, said ink jet recording sheet not only has superior ink absorbency and ink coloration, but also has superior light resistance, water resistance and surface gloss, therefore the ink jet recording paper is of extremely high quality,
  • the average primary particle size of colloidal silica is measured by BET method, the average secondary particle length of non-spherical cationic colloidal silica is measured by laser scattering method.
  • the ink jet recording sheets in the following examples and comparative examples are evaluated by the following method. Unless otherwise noted, all "parts" are by weight in the following examples and comparative examples. The weight in the coating solution is based on dry basis, excluding water.
  • the 75 degree specular glossiness is determined by using a glossimeter, GM-26D (trade name, a product of Murakami Shikisai Kenkyujo), in accordance to JIS P8142.
  • the predetermined solid pattern or image pattern is printed on the test sheet by an ink jet printer, Model PM750C (trade name, a product of Seiko Epson Corp.) and the various properties of the recorded sheet is evaluated by the following method:
  • the reflection densities of the black solid areas are measured with a Macbeth densitometer, RD 915 (trade name, a product of Macbeth Limited).
  • the recorded density of magenta ink is measured after being tested for 25 hours by Xenon Weather Meter SC700-WN (trade name, a product of Suga Test Machinery Limited), and evaluated the remaining recorded density compared with the density before the test according to the ranks mentioned below;
  • the ink absorbency is evaluated by an extent of bleeding at the boundary between image areas of solid magenta and solid green (mixture of cyan and yellow) according to the ranks mentioned below;
  • the recorded image is dried in the air for 1 day, then is immersed in a tap water at 20 degree C for 5 minutes and dried in the air again. Then the extent of change-of recorded images is evaluated according to the ranks mentioned below;
  • a slurry consisting of 93 parts of LBKP (hardwood bleached pulp) with a freeness of 440 ml, 7 parts of NBKP(softwood bleached pulp) with a freeness of 520 ml, 7 parts of talc, 1.5 parts of sulfuric acid band (aluminum sulfate), 0.4 parts of sizing agent and 0.02 parts of yield improver is prepared.
  • Paper is manufactured from the slurry by a twin wire machine and pre-dried by a cylinder drier. Then the coating solution 1 below is applied to the paper by a two roll sizing press to have a total solid coverage of both sides of 4 g/m 2 and is subjected to a machine calender treatment.
  • a base paper with a dry coverage of 157 g/m 2 and a smoothness of 35 seconds is obtained.
  • the coating solution 2 below is coated on one surface of the obtained base paper by means of a Mayer bar so as to have a dry coverage of 13 g/m 2 .
  • the paper is then subjected to a calendering machine with a linear pressure of 80 Kg/cm to produce an ink-receiving layer.
  • an image-preserving layer is formed by coating the coating solution 3 below on the ink-receiving layer by means of a Mayer bar so as to have a dry coverage of 2 g/m 2 and then calendered at a linear pressure of 100 Kg/cm.
  • An ink jet recording sheet with a dry coverage of 172 g/m 2 is obtained.
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that Fine Zinc Oxide (registered trade mark of Honjo Chemical) with an average particle size of 200 nm is used for zinc oxide particulates in the coating solution 3.
  • Fine Zinc Oxide registered trade mark of Honjo Chemical
  • the inkjet recording sheet is obtained in the same manner as in Example 1, except that the content of the zinc oxide particulates is 15 parts in the coating solution 3.
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that the dry coverage of the coating solution 3 is 4.5 g/m 2 .
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that the dry coverage of the coating solution 3 is 10 g/m 2 .
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that the coating solution 2 is not applied.
  • the inkjet recording sheet is obtained in the same manner as in Example 1, except that Hydrozincite No.1 (registered trade mark of Sakai Chemical) with an average particle size of 520 nm is used for zinc oxide particulates in the coating solution 3.
  • Hydrozincite No.1 registered trade mark of Sakai Chemical
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that FINEX-75 (a product of Sakai Chemical) with an average particle size of 10 nm is used for zinc oxide particulates in the coating solution 3.
  • FINEX-75 a product of Sakai Chemical
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that the coating solution 3 is not applied.
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that the zinc oxide particulates is not formulated in the coating solution 3.
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that the colloidal silica is not formulated in the coating solution 3.
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that Synthetic amorphous silica, Fineseal X-37B(Tokuyama), is used for the colloidal silica in the coating solution 3.
  • Example 1 The evaluation results for Examples 1 to 6 and Comparative examples 1 to 6 are summarized in Table 1 below.
  • the ink jet recording sheets ranked by o ⁇ or ⁇ can be used without causing problems.
  • Example 1 35.8 2.10 o ⁇ o ⁇
  • Example 2 30.8 2.01 o ⁇ o ⁇
  • Example 3 30.4 1.95 o ⁇ o ⁇
  • Example 4 41.7 1.99 o ⁇ o ⁇
  • Example 5 43.6 2.06 o ⁇ ⁇
  • Example 6 30.5 1.98 o ⁇ ⁇ Comparative Example 1 19.4 1.62 ⁇ ⁇ Comparative Example 2 44.1 1.90 o ⁇ ⁇ Comparative Example 3 7.8 1.84 ⁇ o ⁇ Comparative Example 4 45.8 2.08 ⁇ ⁇ Comparative Example 5 8.3 1.60 ⁇ ⁇ Comparative Example 6 8.3 1.79 ⁇ o ⁇
  • a slurry consisted of 93 parts of LSKP with a freeness of 440 ml (csf), 7 parts of NBKP with a freeness of 520 ml (csf), 7 parts of talc, 1.5 parts of sulfuric acid band, 0.4 parts of sizing agent and 0.02 parts of yield improver is prepared.
  • a paper is manufactured from the slurry by a twin wire machine and pre-dried by a cylinder drier.
  • oxidized starch is applied to the both sides of the paper by a two roll sizing press to have a total solid coverage of both sides of 4 g/m 2 , followed by a machine calender treatment.
  • a base paper with a dry coverage of 160 g/m 2 and a smoothness of 35 seconds is obtained.
  • the coating solution 4 below is coated on one surface of the obtained base paper by means of a Mayer bar so as to have a dry coverage of 16 g/m 2 .
  • the paper is then subjected to a calendering machine with a linear pressure of 80 Kg/cm to form an ink-receiving layer.
  • coating solutions 5 and 6 below are coated successively on the ink-receiving layer by means of a Mayer bar so as to have a dry coverage of 2 g/m 2 each to form a image-preserving layer and a fixing layer, and the paper is subjected to a calendering machine with a linear pressure of 100 Kg/cm.
  • An ink jet-recording sheet with a dry coverage of 180 g/m 2 is obtained.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that the average particle size of the zinc oxide particulate is 200 nm in coating solution 5.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that the content of the zinc oxide particulates is 15 parts in coating solution 5.
  • the ink jet recording sheet with a dry coverage of 182.5 g/m 2 is obtained in the same manner as in Example 7, except that the dry coverage of coating solution 5 is 4.5 g/m 2 .
  • the ink jet recording sheet with a dry coverage of 188 g/m 2 is obtained in the same manner as in Example 7, except that the dry coverage of coating solution 5 is 10 g/m 2 .
  • the ink jet recording sheet wich a dry coverage of 164 g/m 2 is obtained in the same manner as in Example 7, except that coating solution 4 is not applied.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that spherical cationic colloidal silica Snowtex O with an average primary particle size of 10 to 20 nm (Nissan Chemical) is used for the non-spherical (beads type) cationic colloidal silica in coating solution 6.
  • spherical cationic colloidal silica Snowtex O with an average primary particle size of 10 to 20 nm is used for the non-spherical (beads type) cationic colloidal silica in coating solution 6.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that zinc oxide particulates with an average particle size of 520 nm is used for zinc oxide particulates in coating solution 5.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that zinc oxide particulates with an average particle size of 10 nm is used for the zinc oxide particulates in coating solution 5.
  • the ink jet recording sheet with a dry coverage of 178 g/m 2 is obtained in the same manner as in Example 7, except that coating solution 5 is not applied.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that the spherical anionic colloidal silica is not formulated in coating solution 5.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that the zinc oxide particulate is not formulated in coating solution 5.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that the non-spherical cationic colloidal silica is not formulated in coating solution 6.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that the cationic polymer electrolyte is not formulated in coating solution 6.
  • the inkjet recording sheet is obtained in the same manner as in Example 7, except that synthetic amorphous silica with an average secondary particle size of 4 ⁇ m, Fineseal X-37B (Tokuyama), is used for the spherical anionic colloidal silica in coating solution 5.
  • Example 7 The evaluation results for Examples 7 to 13 and Comparative examples 7 to 14 are summarized in Table 2 below.
  • the ink jet recording sheets ranked by o ⁇ or ⁇ can be used without causing problems.
  • Example 7 40.6 2.21 o ⁇ o ⁇ o ⁇
  • the ink jet recording sheet of the present invention provides a superior combination of ink absorbency, ink coloration, light resistance, water resistance and surface gloss even when printed with an ink containing a water-soluble dye.
  • the ink jet recording sheet is obtained in the same manner as in Example 1, except that coating solution 7 below is used instead of coating solution 2.
  • the ink jet recording sheet is obtained in the same manner as in Example 14, except that the content of the hindered amine compound (Tinuvin 123) is 10 parts in the coating solution 7.
  • the ink jet recording sheet is obtained in the same manner as in Example 14, except that the benzotriazole compound is omitted from coating solution 7.
  • the ink jet recording sheet is obtained in the same manner as in Example 7, except that coating solution 7 is used for the coating solution 4.
  • the ink jet recording sheet is obtained in the same manner as in Example 17, except that the content of the hindered amine compound (Tinuvin 123) is 10 parts in coating solution 7.
  • the ink jet recording sheet is obtained in the same manner as in Example 17, except that the benzotriazole compound is omitted from coating solution 7.
  • An ink jet recording sheet is obtained in the same manner as in Example 17, except that Tinuvin 144 (Ciba Specialty Chemicals, Inc.) of the formula (2) below is used instead of the hindered amine compound (Tinuvin 123) in coating solution 7. ,where R 2 is
  • the ink jet recording sheet is obtained in the same manner as in Example 17, except that Tinuvin 292 (Ciba Specialty Chemicals, Inc.) of the formula (3) below is used for the hindered amine compound (Tinuvin 123) in coating solution 7. ,where R 2 is C 8 H 16 .
  • Examples 14 to 19 that the light resistance is further improved by formulating Tinuvin 123, hindered amine compound of amino ether type having alkoxyl groups of formula (1), in the ink-receiving layer.
  • the light resistance is further improved by formulating benzotriazole compound in the ink-receiving layer.
  • comparative examples 15 and 16 formulating hindered amine compound of formula (2) or (3), there is not such improvement in light resistance as in examples 14 to 19.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Ink Jet Recording Methods And Recording Media Thereof (AREA)

Description

    Field of the Invention
  • The present invention relates to a recording material that can be print on with ink containing water-soluble dye. In particular, the present invention relates to an ink jet recording sheet which provides a superior combination of ink absorbency, ink coloration, resistance of the recorded image to light, resistance of the recorded image to water and surface gloss.
  • Prior Art
  • Ink jet recording is a method by which fine ink drops are jetted out using any kind of jetting method to form an image on a recording material. Since this method enables a recording apparatus to be operated at a high speed and the apparatus is generally inexpensive, the use of ink jet recording systems has been spreading rapidly. Moreover, the use of multicolor ink jet recording methods enables the formation of color images comparable to silver-salt films with high resolution and high quality. Digital images, for example those obtained by a digital camera, are increasingly printed with an ink jet printer. The recorded materials are more often being displayed or stored for considerably long period because of the high image quality. Therefore, it is desirable that the ink jet recording materials have good preservation characteristics, especially good light resistance, as well as high image quality.
  • Ordinary ink jet recording sheets, printed by an ink jet printer, are discolored by the UV light in the sunlight or fluorescent lamps. Therefore some countermeasures for this problem have been attempted to improve the long-term preservation properties of the sheet. Although some attempts utilized a pigment ink system with a pigment resistant to discoloration, in most instances it is attempted to improve the light resistance by using a dye ink system because dye ink system provide sharper images.
  • As examples of means to improve the light resistance, for example, a process to add UV absorber such as benzophenones and benzotriazoles (Japanese Tokkai Sho 57-87988 and Japanese Tokkai Sho 63-222885, "Tokkai" means an "unexamined published patent application"), a process to add antioxidant such as hindered amines (Japanese Tokkai Sho 61-146591), a process to add zinc oxide and cationic resins concurrently (Japanese Tokkai Hei 7-32725) and the like have been disclosed. However, since these additives are difficult to disperse evenly in the materials, these attempts did not provide a satisfactory improvement.
  • As a method to attain the high image quality by increasing the gloss of the recording sheet, for example, a process to use cationic colloidal silica (Japanese Tokkai Hei 6-92011) has been proposed, but this process can not provide a sufficient balance between the image quality and the image preservation.
  • Moreover, a process to improve the water resistance of the recording layer by setting up a coating layer comprising a colloidal silica that couples like beads and a water-soluble polymer (Japanese Tokkai Hei 5-51469) have been proposed, but this process can not achieve sufficient water resistance and its light resistance is still insufficient.
  • Problems Encountered
  • The objective of this invention is to provide a recording material that can be recorded by ink with water-soluble dye, particularly to provide an ink jet recording sheet, which is superior in ink absorbency, ink coloration, light resistance, water resistance and surface gloss.
  • Summary of the Invention
  • One subject of the present invention is an ink jet recording sheet having on an ink-receiving support an image preserving layer comprising anionic colloidal silica and zinc oxide particulates with an average particle size of about 15 to 380 nm and having a 75 degree specular glossiness of at least about 25% at the surface. Another subject of the present invention is an ink jet recording sheet having on an ink-receiving support, in succession, an image preserving layer comprising an anionic colloidal silica and zinc oxide particulates with an average particle size of about 15 to 380 nm and a fixing layer comprising a cationic colloidal silica and a cationic polymer electrolyte.
  • Detailed Description of the Invention
  • The support used in the present invention may be any of known supports capable of absorbing an ink containing a water-soluble dye, is preferably a support having an ink-receiving layer comprising a pigment and a binder on a base paper.
  • The image preserving layer formed on the ink-receiving layer mentioned before comprises zinc oxide particulates with an average particle size of about 15 to 380 nm, preferably about 20 to 300 nm, which absorbs UV light, and anionic colloidal silica, which is compatible with said particulates and can provide a glossy surface property in order to obtain compatibility between the light resistance and the high quality of recorded image.
  • Colloidal silica of this invention is the stabilized colloidal solution of silica to make its utilization easy, as described in Kagaku Binran (Chemical Reference Guide) published by Maruzen, Oct.15, 1986.
  • When the average particle size of zinc oxide particulates is less than 15 nm, the image-preserving layer is very closely packed and therefore has a poor ink absorbency, which not only makes it difficult to obtain images of high quality but also causes problems in cost and operability. On the other hand, when the average particle size is larger than 380 nm, the transparency of the image-preserving layer becomes worse due to light scattering thereby reducing the recorded density. The average particle size of zinc oxide particulates is measured by using a scanning electron microscope.
  • Since the surfaces of the zinc oxide particulates, which are necessary to impart light resistance, are negatively charged, the colloidal silica, which is necessary for glossy surface, needs to be anionic colloidal silica. Since the isoelectric point of anionic silica is usually around pH 2, the silica is negatively charged in the almost all range above pH 2, which is suitable for this invention. On the contrary, the colloidal silica that is reversely charged by having cations, for example, obtained by hydrolysis of metal salts, absorbed on the surface, has problems in operability due to poor compatibility with the zinc oxide particulates.
  • The configuration of the anionic colloidal silica is preferably non-spherical shape, in which several particulates interlink as in a shape of beads or a ring.
  • It is desirable that the coverage of the image-preserving layer be about 1 to 6 g/m2, preferably about 1.5 to 5 g/m2, on a dry solids basis. When the coverage of the image-preserving layer is less than 1 g/m2, sufficient light resistance and surface gloss cannot be attained. On the other hand, when the coverage is larger than 6 g/m2, the ink absorbency of the layer becomes poor and high quality images cannot be obtained.
  • The content of the zinc oxide particulates in the image-preserving layer is desired to be about 2 to 25 parts by weight, preferably about 3 to 20 parts by weight based on the 100 parts by weight of the anionic colloidal silica. When the content of the zinc oxide particulates is less than 2 parts by weight, sufficient light resistance cannot be attained. On the other hand, when the content is larger than 25 parts by weight, the recorded density and the surface gloss become poor and high quality images cannot be obtained.
  • Further, the 75 degree specular glossiness of the image preserving layer needs to be at least about 25%, preferably at least about 30% at the surface, measured in accordance with JIS(Japanese Industrial Standards) P8142, in order to obtain sufficient reproducibility of image similar to a silver salt film.
  • The base paper used for an ink-receiving support of the present invention can be made from various types of paper pulps. Examples of the pulp for paper include chemical pulp such as LBKP (hardwood bleached pulp) and NBKP (softwood bleached pulp), mechanical pulp such as GP(groundwood pulp) and TMP(thermo mechanical pulp), waste paper pulp and mixture thereof, but the pulp is not limited to those.
  • Various additives, such as fillers, sizing agents and paper reinforcing agents, can be added to the base paper, but the additives are not limited to those and can be selected from known fillers and known additives as required. Starch or other surface-sizing agents can be size pressed or coated. Further, antifoaming agents, pH regulators, pigments and coloring dyes for adjusting color, fluorescent pigments for improving visual whiteness and the like can be added as well.
  • It is desirable that the coverage of the ink-receiving layer formed on the base paper be about 5 to-25 g/m2, preferably about 7 to 20 g/m2, on a dry solids basis. When the coverage of the ink-receiving layer is less than 5 g/m2, the ink absorbency of the layer becomes poor which will cause bleeding of ink. On the other hand, when the coverage is larger than 25 g/m2, the amount of absorbed ink becomes excessive thereby reducing the recording density and this will also degrade the quality of image.
  • The ink-receiving layer comprises pigment and binder. For pigment, white pigment, such as light and heavy calcium carbonate, kaolin, clay, talc, titanium dioxide, zinc oxide, satin white, magnesium silicate, calcium silicate, aluminum silicate, aluminum hydroxide, alumina, quasi-boehmite, synthetic amorphous silica, magnesium carbonate, zeolite, is preferred. Among these, synthetic amorphous silica is more preferred as a pigment for the ink-receiving layer because it provides a superior combination of ink coloration, ink absorbency and cost.
  • The binder resin used for the ink-receiving layer can be selected from any resins that can bond strongly to the base paper and can form films when coated and dried. It is desirable to use starches such as oxidized starch, esterified starch, enzyme-modified starch and cationic starch; polyvinyl alcohol with various degrees of saponification and derivatives thereof; casein, soy proteins; cellulose derivatives such as carboxymethyl cellulose and hydroxymethyl cellulose; styrene-acrylic resin; isobutylene-maleic anhydride resin; acrylic emulsion; vinyl acetate emulsion; vinylidene chloride emulsion; polyester emulsion; styrene-butadiene latex; acrylonitrile-butadiene latex and the like.
  • A dye fixing agent that is cationic resin can be added to ink-receiving layer in order to impart water resistance property of the image. Examples of such agents include dicyandiamide-alkylamine polycondensed material, dicyanodiamide-formaldehyde polycondensed material, polyethylene-imine derivatives, alkylamine(-ammonium)-epichlorohydrin polycondensed material, polymethacrylic acid quaternary ammonium salt derivatives, polydiallyl-dimethyl-ammonium chloride, and other commercially available dye fixing agent. Mixtures of these can also be used without the loss of the advantage of the present invention.
  • The fixing layer of the present invention comprises cationic colloidal silica and cationic polymer electrolyte and provide a good combination of light resistance, water resistance and surface gloss. Further, it is preferred that the configuration of the cationic colloidal silica is non-spherical shape, in which several particulates interlink as in a shape of beads or a ring. When the fixing layer contains anionic colloidal silica or synthetic amorphous silica, problems are seen in operability due to the poor compatibility of the silica with the cationic polymer electrolyte.
  • It is desirable that the coverage of the fixing layer be about 1 to 6 g/m2, preferably about 1.5 to 5 g/m2, on a dry solids basis. When the coverage of the fixing layer is less than 1 g/m2, sufficient water resistance and surface gloss cannot be attained. On the other hand, when the coverage is larger than 6 g/m2, the ink absorbency of the layer-becomes poor and high quality images cannot be obtained.
  • The content of the cationic polymer electrolyte in the fixing layer is desired to be about 2 to 25 parts by weight, preferably about 3 to 20 parts by weight based on the 100 parts by weight of the cationic colloidal silica. When the content of the cationic polymer electrolyte is less than 2 parts by weight, the water resistance is sometimes insufficient. On the other hand, when the content is larger than 25 parts by weight, the ink absorbency and light resistance sometimes degrades.
  • The cationic polymer electrolyte of the present invention can be selected from dicyandiamide-alkylamine polycondensed material, dicyanodiamide-formaldehyde polycondensed material, polyethylene-imine derivatives, alkylamine (-ammonium)-epichlorohydrin polycondensed material, polymethacrylic acid quaternary ammonium salt derivatives, polydiallyl-dimethyl-ammonium chloride, other commercially available cationic polymer electrolyte and mixture thereof.
  • By applying the fixing layer comprising cationic colloidal silica and cationic polymer electrolyte as a top layer, it becomes possible to obtain compatibility between water resistance and quality of recorded images. In order to get a reproducibility of images comparable to silver-salt films, the 75 degree specular glossiness is desirably at least about 30%, preferably at least about 35% at the surface of the fixing layer, measured in accordance with JIS(Japanese Industrial Standards) P8142.
  • Further, the ink-receiving layer may comprise hindered amine compounds of amino ether type having alkoxyl groups in order to impart light resistance. Suitable hindered amine compounds are represented by formula (1) below:
    Figure 00090001
    wherein R1 is CnH2n+1 (n= 1 to 14), R2 is CnH2n (n= 1 to 14) and R3 to R6 are each an alkyl group or carbonyl group. Benzotriazole compounds may be used together to improve the light resistance further.
  • The n in R1 and R2 of the formula (1) is preferably 6 to 10, and the alkyl group or carbonyl group of R3 to R6 is preferably a lower alkyl group with 1 to 4 carbons, more preferably methyl group.
  • The hindered amine compound of the amino ether type having alkoxyl groups is preferably bis-(2,2,6,-tetramethyl-1-(octyloxy)-4-piperidinyl)sebacate wherein R1 is C8H17, R2 is C3H15 and R3 to R6 are methyl groups in the formula (1) (Tinuvin 123, manufactured by Ciba Specialty Chemicals, Inc.).
  • Hindered amine compounds generally generate nitroxy radicals by reacting with hydroperoxide or triplet oxygen in the air, which further react to form aminoethers by capturing polymer radicals generated by photodegradation of dyes contained in ink. Then the generated aminoethers react with peroxy radicals generated by a reaction between polymer radicals and oxygen in the air to regenerate nitroxy radicals. The aminoether also releases olefins, simultaneously generating hydroxylamine that react with the peroxy radicals to regenerate nitroxy radicals. This process is repeated to capture the radicals and hamper a chain reaction, thereby preventing the image from photodegrading.
  • Since the hindered amine compounds of the present invention have an amino ether as part of their chemical structure, it is considered that peroxy radicals are immediately captured when generated. Thus the hindered amine compound is very effective in preventing photodegradation of image. While in the case of conventional hindered amine compounds unsubstituted or substituted by alkyl or acetyl groups, it is considered that there is a large energy barrier to producing aminoethers, which inhibit the effective prevention of photodegradation.
  • The content of the hindered amine compounds in the ink-receiving layer is desired to be about 0.5 to 15 wt%, preferably about 2 to 8 wt%. When the content of the compounds is less than 0.5 wt%, the addition of the compounds would not be effective, and when the content is larger than 15 wt%, the applicability in manufacturing becomes worse.
  • The benzotriazole compounds of the present invention preferably include, for example, 2-(2-hydroxy-3,5-di-t-amylphenyl-2H-benzotriazole, iso-octyl-3,3-(2H-benzotriazole-2-yl)-5-t-butyl-4-hydroxyphenylpropionate, 2-[2-hydroxy-3,5-di(1,1-dimethylbenzyl)phenyl]-2H-benzotriazole, 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole, and the like.
  • The content of the benzotriazole compounds in the ink-receiving layer is desired to be about 0.5 to 12 wt%, preferably about 2.5 to 8 wt%. When the content of the benzotriazole compounds is less than 0.5 wt%, the addition of the compounds would not be effective, and when the content is larger than 12 wt%, it causes significant coloring in the applied layer.
  • The coating compositions for the ink-receiving layers, image-preserving layers and fixing layers may contain various additives, such as an antifoaming agent, a surface-sizing agent, a pH-adjusting agent, other CV absorber, an antioxidant, a dye or coloring pigment for adjusting color phase, a fluorescent dye and mixture thereof without the loss of the effect of the present invention.
  • The method of coating the ink-receiving layers, image-preserving layers and fixing layers on base paper includes conventional coaters of various kinds, e.g., a blade coater, an air knife coater, a roll coater, a curtain coater, a bar coater, a gate roll coater and a gravure coater and the like. Further various calendering treatments such as a machine calender, a soft calender, and a super calender can be used solely or in combination for finishing the surface.
  • The ink jet recording sheet of the present invention has on an ink-receiving support, in succession, an image preserving layer comprising zinc oxide particulates with a certain particular size to absorb UV light and anionic colloidal silica that is compatible with the particulates and a fixing layer comprising cationic colloidal silica to impart water resistance and surface gloss. Therefore, said ink jet recording sheet not only has superior ink absorbency and ink coloration, but also has superior light resistance, water resistance and surface gloss, therefore the ink jet recording paper is of extremely high quality,
  • The present invention will now be illustrated in more detail by reference to the following examples, but it should be understood that these examples are not to be construed as limiting the scope of the present invention as defined in the appended claims in any way.
  • Examples
  • The average primary particle size of colloidal silica is measured by BET method, the average secondary particle length of non-spherical cationic colloidal silica is measured by laser scattering method. The ink jet recording sheets in the following examples and comparative examples are evaluated by the following method. Unless otherwise noted, all "parts" are by weight in the following examples and comparative examples. The weight in the coating solution is based on dry basis, excluding water.
  • (1) 75 degree specular glossiness
  • The 75 degree specular glossiness is determined by using a glossimeter, GM-26D (trade name, a product of Murakami Shikisai Kenkyujo), in accordance to JIS P8142.
  • (2) ink jet recording properties
  • The predetermined solid pattern or image pattern is printed on the test sheet by an ink jet printer, Model PM750C (trade name, a product of Seiko Epson Corp.) and the various properties of the recorded sheet is evaluated by the following method:
  • a. recorded density
  • As to the densities of recorded images, the reflection densities of the black solid areas are measured with a Macbeth densitometer, RD 915 (trade name, a product of Macbeth Limited).
  • b. light resistance
  • The recorded density of magenta ink is measured after being tested for 25 hours by Xenon Weather Meter SC700-WN (trade name, a product of Suga Test Machinery Limited), and evaluated the remaining recorded density compared with the density before the test according to the ranks mentioned below;
  • o ○ : Percentage of remaining recorded density is more than 90%.
  • ○ : Percentage of remaining recorded density is 70 to 90%.
  • Δ : Percentage of remaining recorded density is 50 to 70%.
  • ×: Percentage of remaining recorded density is less than 50%.
  • c. ink absorbency
  • The ink absorbency is evaluated by an extent of bleeding at the boundary between image areas of solid magenta and solid green (mixture of cyan and yellow) according to the ranks mentioned below;
  • o ○ : No bleeding is observed at the boundaries.
  • ○ : Almost no bleeding is observed at the boundaries.
  • Δ : Some bleeding is observed at the boundaries.
  • × : Significant bleeding is observed at the boundaries.
  • d. water resistance
  • The recorded image is dried in the air for 1 day, then is immersed in a tap water at 20 degree C for 5 minutes and dried in the air again. Then the extent of change-of recorded images is evaluated according to the ranks mentioned below;
  • × : No change is observed.
  • ○ : Slight change is observed.
  • Δ : Some change is observed.
  • × : Most of the image bleed.
  • Example 1
  • A slurry consisting of 93 parts of LBKP (hardwood bleached pulp) with a freeness of 440 ml, 7 parts of NBKP(softwood bleached pulp) with a freeness of 520 ml, 7 parts of talc, 1.5 parts of sulfuric acid band (aluminum sulfate), 0.4 parts of sizing agent and 0.02 parts of yield improver is prepared. Paper is manufactured from the slurry by a twin wire machine and pre-dried by a cylinder drier. Then the coating solution 1 below is applied to the paper by a two roll sizing press to have a total solid coverage of both sides of 4 g/m2 and is subjected to a machine calender treatment. A base paper with a dry coverage of 157 g/m2 and a smoothness of 35 seconds is obtained.
  • Coating solution 1
    • Water soluble polymer: oxidized starch MS#3600(Nihon Shokuhin Kakou)   100 parts
    • Surface sizing agent: Hamacoat S-200L(Misawa Ceramics)   2 parts
    • Antifoaming agent: Nopco 8034L(Sun-Nopco)   0.1 parts
    • Water   900 parts
  • The coating solution 2 below is coated on one surface of the obtained base paper by means of a Mayer bar so as to have a dry coverage of 13 g/m2. The paper is then subjected to a calendering machine with a linear pressure of 80 Kg/cm to produce an ink-receiving layer. Then an image-preserving layer is formed by coating the coating solution 3 below on the ink-receiving layer by means of a Mayer bar so as to have a dry coverage of 2 g/m2 and then calendered at a linear pressure of 100 Kg/cm. An ink jet recording sheet with a dry coverage of 172 g/m2 is obtained.
  • Coating solution 2
    • Synthetic amorphous silica: Fineseal X-37B(Tokuyama)   100 part
    • Water soluble polymer: PVA-117(Kurarey Co., Ltd.)   15 parts
    • Dye fixing agent: PAS-H-10L(Nitto Boseki)   5 parts
    • Antifoaming agent: SN defoamer 480(Sun-Nopco)   0.1 parts
    • Water   550 parts
    Coating solution 3
    • Non-spherical anionic colloidal silica: Snowtex UP with an average primary particle size of 10 to 20 nm and an average secondary particle length of 50 to 300 nm (Nissan Chemical) 100 parts
    • Zinc oxide particulates: FINEX-50 with an average particle size of 20 nm(Sakai Chemical)   5 parts
    • Antifoaming agent: KM-72F(Shin-Etsu Chemical) 0.1 parts
    • Water   420 parts
    Example 2
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that Fine Zinc Oxide (registered trade mark of Honjo Chemical) with an average particle size of 200 nm is used for zinc oxide particulates in the coating solution 3.
  • Example 3
  • The inkjet recording sheet is obtained in the same manner as in Example 1, except that the content of the zinc oxide particulates is 15 parts in the coating solution 3.
  • Example 4
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that the dry coverage of the coating solution 3 is 4.5 g/m2.
  • Example 5
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that the dry coverage of the coating solution 3 is 10 g/m2.
  • Example 6
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that the coating solution 2 is not applied.
  • Comparative Example 1
  • The inkjet recording sheet is obtained in the same manner as in Example 1, except that Hydrozincite No.1 (registered trade mark of Sakai Chemical) with an average particle size of 520 nm is used for zinc oxide particulates in the coating solution 3.
  • Comparative Example 2
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that FINEX-75 (a product of Sakai Chemical) with an average particle size of 10 nm is used for zinc oxide particulates in the coating solution 3.
  • Comparative Example 3
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that the coating solution 3 is not applied.
  • Comparative Example 4
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that the zinc oxide particulates is not formulated in the coating solution 3.
  • Comparative Example 5
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that the colloidal silica is not formulated in the coating solution 3.
  • Comparative Example 6
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that Synthetic amorphous silica, Fineseal X-37B(Tokuyama), is used for the colloidal silica in the coating solution 3.
  • The evaluation results for Examples 1 to 6 and Comparative examples 1 to 6 are summarized in Table 1 below. The ink jet recording sheets ranked by o ○ or ○ can be used without causing problems.
    75 degree specular glossiness (%) ink jet recording properties
    recorded density light resistance ink absorbency
    Example 1 35.8 2.10 o ○ o ○
    Example 2 30.8 2.01 o ○ o ○
    Example 3 30.4 1.95 o ○ o ○
    Example 4 41.7 1.99 o ○ o ○
    Example 5 43.6 2.06 o ○
    Example 6 30.5 1.98 o ○
    Comparative Example 1 19.4 1.62 Δ
    Comparative Example 2 44.1 1.90 o ○ Δ
    Comparative Example 3 7.8 1.84 × o ○
    Comparative Example 4 45.8 2.08 ×
    Comparative Example 5 8.3 1.60 Δ
    Comparative Example 6 8.3 1.79 Δ o ○
  • Example 7
  • A slurry consisted of 93 parts of LSKP with a freeness of 440 ml (csf), 7 parts of NBKP with a freeness of 520 ml (csf), 7 parts of talc, 1.5 parts of sulfuric acid band, 0.4 parts of sizing agent and 0.02 parts of yield improver is prepared. Then a paper is manufactured from the slurry by a twin wire machine and pre-dried by a cylinder drier. Then oxidized starch is applied to the both sides of the paper by a two roll sizing press to have a total solid coverage of both sides of 4 g/m2, followed by a machine calender treatment. A base paper with a dry coverage of 160 g/m2 and a smoothness of 35 seconds is obtained.
  • Then the coating solution 4 below is coated on one surface of the obtained base paper by means of a Mayer bar so as to have a dry coverage of 16 g/m2. The paper is then subjected to a calendering machine with a linear pressure of 80 Kg/cm to form an ink-receiving layer. To form an image preserving layer, coating solutions 5 and 6 below are coated successively on the ink-receiving layer by means of a Mayer bar so as to have a dry coverage of 2 g/m2 each to form a image-preserving layer and a fixing layer, and the paper is subjected to a calendering machine with a linear pressure of 100 Kg/cm. An ink jet-recording sheet with a dry coverage of 180 g/m2 is obtained.
  • Coating solution 4
    • Synthetic amorphous silica: Fineseal X-37B with an average secondary particle size of 4 µm (Tokuyama)
    Coating solution 4
    • Synthetic amorphous silica: Fineseal X-37B with an average secondarey particle size of 4 µm (Tokuyama)   100 parts
    • Polyvinyl alcohol: PVA-117(Kurarey Co., Ltd.)   20 parts
    • Dye fixing agent(quaternary ammonium salt type polymer) 5 parts
    • Water   550 parts
    Coating solution 5
    • Spherical anionic colloidal silica: Snowtex 20 with an average primary particle size of 10 to 20 nm (Nissan Chemical)   100 parts
    • Zinc oxide particulates with an average particle size of 20 nm   5 parts
    • Water   420 parts
    Coating solution 6
    • Non-spherical (beads type) cationic colloidal silica: Snowtex OUP with an average primary particle size of 10 to 20 nm and secondary particle length of 50 to 300 nm (Nissan Chemical)   100 parts
    • Cationic polymer electrolyte (quaternary ammonium salt type polymer)   5 parts
    • Water   550 parts
    Example 8
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that the average particle size of the zinc oxide particulate is 200 nm in coating solution 5.
  • Example 9
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that the content of the zinc oxide particulates is 15 parts in coating solution 5.
  • Example 10
  • The ink jet recording sheet with a dry coverage of 182.5 g/m2 is obtained in the same manner as in Example 7, except that the dry coverage of coating solution 5 is 4.5 g/m2.
  • Example 11
  • The ink jet recording sheet with a dry coverage of 188 g/m2 is obtained in the same manner as in Example 7, except that the dry coverage of coating solution 5 is 10 g/m2.
  • Example 12
  • The ink jet recording sheet wich a dry coverage of 164 g/m2 is obtained in the same manner as in Example 7, except that coating solution 4 is not applied.
  • Example 13
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that spherical cationic colloidal silica Snowtex O with an average primary particle size of 10 to 20 nm (Nissan Chemical) is used for the non-spherical (beads type) cationic colloidal silica in coating solution 6.
  • Comparative Example 7
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that zinc oxide particulates with an average particle size of 520 nm is used for zinc oxide particulates in coating solution 5.
  • Comparative Example 8
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that zinc oxide particulates with an average particle size of 10 nm is used for the zinc oxide particulates in coating solution 5.
  • Comparative Example 9
  • The ink jet recording sheet with a dry coverage of 178 g/m2 is obtained in the same manner as in Example 7, except that coating solution 5 is not applied.
  • Comparative Example 10
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that the spherical anionic colloidal silica is not formulated in coating solution 5.
  • Comparative Example 11
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that the zinc oxide particulate is not formulated in coating solution 5.
  • Comparative Example 12
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that the non-spherical cationic colloidal silica is not formulated in coating solution 6.
  • Comparative Example 13
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that the cationic polymer electrolyte is not formulated in coating solution 6.
  • Comparative Example 14
  • The inkjet recording sheet is obtained in the same manner as in Example 7, except that synthetic amorphous silica with an average secondary particle size of 4 µm, Fineseal X-37B (Tokuyama), is used for the spherical anionic colloidal silica in coating solution 5.
  • The evaluation results for Examples 7 to 13 and Comparative examples 7 to 14 are summarized in Table 2 below. The ink jet recording sheets ranked by o ○ or ○ can be used without causing problems.
    75 degree specular glossiness (%) ink jet recording properties
    recorded density light resistance ink absorbency water resistance
    Example 7 40.6 2.21 o ○ o ○ o ○
    Example 8 39.5 2.14 o ○ o ○ o ○
    Examples 9 36.0 2.01 o ○ o ○ o ○
    Example 10 43.9 2.20 o ○ o ○ o ○
    Example 11 47.8 2.15 o ○
    Example 12 37.2 1.97 o ○
    Example 13 46.1 2.06 o ○
    Comparative Example 7 23.9 1.81 Δ
    Comparative Example 8 44.4 2.15 o ○ Δ o ○
    Comparative Example 9 29.5 2.04 × o ○ o ○
    Comparative Example 10 can not be measured because of weakness of image-preserving layer
    Comparative Example 11 43.2 1.89 × o ○ o ○
    Comparative Example 12 20.5 1.92 o ○ Δ
    Comparative Example 13 41.5 2.00 o ○ Δ
    Comparative Example 14 19.2 1.79 Δ o ○
  • It is obvious from Tables 1 and 2 that the ink jet recording sheet of the present invention provides a superior combination of ink absorbency, ink coloration, light resistance, water resistance and surface gloss even when printed with an ink containing a water-soluble dye.
  • Example 14
  • The ink jet recording sheet is obtained in the same manner as in Example 1, except that coating solution 7 below is used instead of coating solution 2.
  • Coating solution 7
    • Synthetic amorphous silica: Fineseal X-37B(Tokuyama) 100 parts
    • Water soluble polymer: PVA-117(Kurarey Co., Ltd.)   15 parts
    • Dye fixing agent: PAS-H-10L(Nitto Boseki)   5 parts
    • Hindered amine compound: bis-(2,2,6,6-tetramethyl-1-(octyloxy)-4-piperidinyl) sebacate (Tinuvin 123, manufactured by Ciba Specialty Chemicals, Inc.)   3 parts
    • Benzotriazole compound: Tinuvin 900 (Ciba Specialty Chemicals Inc.)   10 parts
    • Antifoaming agent: SN defoamer 480(Sun-Nopco) 0.1 parts
    • Water   550 parts
    Example 15
  • The ink jet recording sheet is obtained in the same manner as in Example 14, except that the content of the hindered amine compound (Tinuvin 123) is 10 parts in the coating solution 7.
  • Example 16
  • The ink jet recording sheet is obtained in the same manner as in Example 14, except that the benzotriazole compound is omitted from coating solution 7.
  • Example 17
  • The ink jet recording sheet is obtained in the same manner as in Example 7, except that coating solution 7 is used for the coating solution 4.
  • Example 18
  • The ink jet recording sheet is obtained in the same manner as in Example 17, except that the content of the hindered amine compound (Tinuvin 123) is 10 parts in coating solution 7.
  • Example 19
  • The ink jet recording sheet is obtained in the same manner as in Example 17, except that the benzotriazole compound is omitted from coating solution 7.
  • Comparative Example 15
  • An ink jet recording sheet is obtained in the same manner as in Example 17, except that Tinuvin 144 (Ciba Specialty Chemicals, Inc.) of the formula (2) below is used instead of the hindered amine compound (Tinuvin 123) in coating solution 7.
    Figure 00250001
    ,where R2 is
    Figure 00250002
  • Comparative Example 16
  • The ink jet recording sheet is obtained in the same manner as in Example 17, except that Tinuvin 292 (Ciba Specialty Chemicals, Inc.) of the formula (3) below is used for the hindered amine compound (Tinuvin 123) in coating solution 7.
    Figure 00260001
    ,where R2 is C8H16.
  • It is obvious from Examples 14 to 19 that the light resistance is further improved by formulating Tinuvin 123, hindered amine compound of amino ether type having alkoxyl groups of formula (1), in the ink-receiving layer. The light resistance is further improved by formulating benzotriazole compound in the ink-receiving layer. On the other hand, in comparative examples 15 and 16, formulating hindered amine compound of formula (2) or (3), there is not such improvement in light resistance as in examples 14 to 19.

Claims (11)

  1. An ink jet recording sheet having on an ink-receiving support an image preserving layer comprising anionic colloidal silica and zinc oxide particulates with an average particle size of about 15 to 380 nm, wherein said sheet has a 75 degree specular glossiness of at least about 25 % at the surface, measured in accordance with JIS P8142.
  2. An ink jet recording sheet having on an ink-receiving support, in succession, an image preserving layer comprising anionic colloidal silica and zinc oxide particulates with an average particle size of about 15 to 380 nm and a fixing layer comprising cationic colloidal silica and cationic polymer electrolyte.
  3. An ink jet recording sheet as in Claim 1 or 2, wherein the amount of said zinc oxide particulates is about 2 to 25 parts by weight based on 100 parts by weight of said anionic colloidal silica.
  4. An ink jet recording sheet as in Claim 2 or Claim 3 as appended thereto, wherein the configuration of said cationic colloidal silica in the fixing layer is non-spherical shape, in which several particulates interlink.
  5. An ink jet recording sheet as in any one of Claims 1-4, wherein the 75 degree specular glossiness is at least about 30% at the surface.
  6. An ink jet recording sheet as in Claim 3, or Claim 4 or 5 as appended thereto wherein the coverage of said image-preserving layer is about 1 to 6 g/m2 on a dry solids basis.
  7. An ink jet recording sheet as in Claim 5 as appended to Claims 2 and 4, wherein the coverage of said image-preserving layer is about 1 to 6 g/m2 on a dry solids basis and the coverage of said fixing layer is about 1 to 6 g/m2 on a dry solids basis.
  8. An ink jet recording sheet as in any one of Claims 1-7, wherein said ink-receiving support has an ink-receiving layer comprising at least a pigment and a binder on a base paper.
  9. An ink jet recording sheet as in Claim 8, wherein the coverage of said ink-receiving layer is about 5 to 25 g/m2 on a dry solids basis.
  10. An ink jet recording sheet as in Claim 8 or 9, wherein said ink-receiving layer comprises hindered amine compounds of amino ether type having alkoxyl groups of formula (1) below:
    Figure 00280001
    wherein R1 is CnH2n+1 (n= 1 to 14), R2 is CnH2n (n= 1 to 14), and R3 to R6 are alkyl group or carbonyl group.
  11. An ink jet recording sheet as in Claim 10, wherein said ink-receiving layer further comprises a benzotriazole compound.
EP99309809A 1998-12-02 1999-12-07 Ink-jet recording sheet with image-protecting layer Expired - Lifetime EP1008457B1 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP10343037A JP2000169873A (en) 1998-12-02 1998-12-02 Silicone grease composition
JP34303798 1998-12-08
JP05060899A JP3300680B2 (en) 1999-02-26 1999-02-26 Inkjet recording paper
JP5060899 1999-02-26
JP6855399 1999-03-15
JP06855399A JP3377464B2 (en) 1999-03-15 1999-03-15 Inkjet recording paper

Publications (2)

Publication Number Publication Date
EP1008457A1 EP1008457A1 (en) 2000-06-14
EP1008457B1 true EP1008457B1 (en) 2003-07-30

Family

ID=27738855

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99309809A Expired - Lifetime EP1008457B1 (en) 1998-12-02 1999-12-07 Ink-jet recording sheet with image-protecting layer

Country Status (2)

Country Link
EP (1) EP1008457B1 (en)
DE (1) DE69909947T2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7655689B2 (en) 2000-06-28 2010-02-02 Bristol-Myers Squibb Company Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
US7655688B2 (en) 2001-02-27 2010-02-02 Bristol-Myers Squibb Company Fused cyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3891546B2 (en) 2000-07-19 2007-03-14 日本製紙株式会社 Inkjet recording medium
GB2371769A (en) * 2001-02-02 2002-08-07 Ilford Imaging Uk Ltd Recording material and method
JP2003123323A (en) * 2001-10-03 2003-04-25 Sony Corp Optical information medium
US7255909B2 (en) 2002-02-19 2007-08-14 3M Innovative Properties Company Security laminate
US20030184636A1 (en) * 2002-02-19 2003-10-02 Graham Paul D. Image receptive material comprising cationically charged inorganic particles
TWI349024B (en) * 2002-03-19 2011-09-21 Grace W R & Co Coating composition comprising colloidal silica and glossy ink jet recording sheets prepared therefrom
TW200307022A (en) 2002-03-19 2003-12-01 W R Grance & Co Conn Coating composition comprising colloidal silica and glossy ink jet recording sheets prepared therefrom
US6902780B2 (en) * 2002-03-19 2005-06-07 W. R. Grace & Co.-Conn Coating composition comprising colloidal silica and glossy ink jet recording sheets prepared therefrom
US6896942B2 (en) * 2002-04-17 2005-05-24 W. R. Grace & Co. -Conn. Coating composition comprising colloidal silica and glossy ink jet recording sheets prepared therefrom
US6833169B2 (en) 2002-10-08 2004-12-21 Hewlett-Packard Development Company, L.P. Porous ink-jet printed media sealed by interpolymer complex
WO2004048116A1 (en) * 2002-11-27 2004-06-10 Mitsubishi Paper Mills Limited Ink-jet recording material
ITSV20040028A1 (en) 2004-06-25 2004-09-25 Ferrania Spa INK JET REGISTRATION MATERIAL
US7658980B2 (en) 2004-08-06 2010-02-09 3M Innovative Properties Company Tamper-indicating printable sheet for securing documents of value and methods of making the same
US7648744B2 (en) 2004-08-06 2010-01-19 3M Innovative Properties Company Tamper-indicating printable sheet for securing documents of value and methods of making the same
ITSV20050003A1 (en) 2005-01-19 2006-07-20 Ferrania Spa MATERIAL FOR INKJET RECORDING

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58110287A (en) * 1981-12-24 1983-06-30 Mitsubishi Paper Mills Ltd Sheet for recording
US5041328A (en) * 1986-12-29 1991-08-20 Canon Kabushiki Kaisha Recording medium and ink jet recording method by use thereof
US5275867A (en) * 1991-02-19 1994-01-04 Asahi Glass Company Ltd. Recording film and recording method
JPH07238478A (en) * 1993-12-28 1995-09-12 New Oji Paper Co Ltd Sheet for ink jet recording

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7655689B2 (en) 2000-06-28 2010-02-02 Bristol-Myers Squibb Company Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
US7655688B2 (en) 2001-02-27 2010-02-02 Bristol-Myers Squibb Company Fused cyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function

Also Published As

Publication number Publication date
DE69909947T2 (en) 2004-02-12
EP1008457A1 (en) 2000-06-14
DE69909947D1 (en) 2003-09-04

Similar Documents

Publication Publication Date Title
EP1008457B1 (en) Ink-jet recording sheet with image-protecting layer
EP1016546B1 (en) Ink-jet recording paper containing silica layers and method for its' manufacture
US6391428B1 (en) Ink jet recording sheet
EP1174279B1 (en) Ink-jet recording material containing ultraviolet ray-absorber
US20080075869A1 (en) Multi-functional paper for enhanced printing performance
EP1036666B1 (en) Ink-jet recording sheet containing aluminium and magnesium salts
CA2605780A1 (en) Coated multipurpose paper, process and compositions thereof
EP1122084B1 (en) Ink-jet recording material suitable for pigment ink
KR20060042134A (en) Ink jet recording sheet
US20050237372A1 (en) Cast Coated Inkjet Paper
US6652931B1 (en) Recording material for ink-jet recording
WO2003076203A1 (en) Ink jet recording sheet
JP2006272939A (en) Manufacturing method of inkjet recording sheet
US7033016B2 (en) Ink-jet recording medium
WO2005032834A1 (en) Recording medium
EP1675727B1 (en) Recording medium
JP2000280607A (en) Ink jet recording sheet
WO2005032832A1 (en) Recording medium
WO2005032836A1 (en) Recording medium
JP2011213010A (en) Inkjet recording paper
WO2005032835A1 (en) Recording medium
WO2006011798A1 (en) Inj jet recording medium
JP2002086902A (en) Ink-jet recording medium and its production method
JP2000168226A (en) Ink jet recording paper
JPH05124329A (en) Material for ink jet recording and its manufacture

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: A1

Designated state(s): DE FR GB

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

17P Request for examination filed

Effective date: 20000830

AKX Designation fees paid

Free format text: DE FR GB

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Designated state(s): DE FR GB

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 69909947

Country of ref document: DE

Date of ref document: 20030904

Kind code of ref document: P

ET Fr: translation filed
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

Effective date: 20040504

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

Ref country code: FR

Payment date: 20081212

Year of fee payment: 10

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

Ref country code: DE

Payment date: 20081205

Year of fee payment: 10

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

Ref country code: GB

Payment date: 20081203

Year of fee payment: 10

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

Effective date: 20091207

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20100831

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: 20091231

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: 20100701

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: 20091207