WO2008038508A1 - Ensemble d'encres pour impression jet d'encre durcissables par ultraviolet et plaque colorée pour une utilisation à l'extérieur imprimée à l'aide dudit ensemble d'encres - Google Patents
Ensemble d'encres pour impression jet d'encre durcissables par ultraviolet et plaque colorée pour une utilisation à l'extérieur imprimée à l'aide dudit ensemble d'encres Download PDFInfo
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- WO2008038508A1 WO2008038508A1 PCT/JP2007/067580 JP2007067580W WO2008038508A1 WO 2008038508 A1 WO2008038508 A1 WO 2008038508A1 JP 2007067580 W JP2007067580 W JP 2007067580W WO 2008038508 A1 WO2008038508 A1 WO 2008038508A1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/40—Ink-sets specially adapted for multi-colour inkjet printing
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0047—Digital printing on surfaces other than ordinary paper by ink-jet printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0081—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using electromagnetic radiation or waves, e.g. ultraviolet radiation, electron beams
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0058—Digital printing on surfaces other than ordinary paper on metals and oxidised metal surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0064—Digital printing on surfaces other than ordinary paper on plastics, horn, rubber, or other organic polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/007—Digital printing on surfaces other than ordinary paper on glass, ceramic, tiles, concrete, stones, etc.
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0076—Digital printing on surfaces other than ordinary paper on wooden surfaces, leather, linoleum, skin, or flowers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
- Y10T428/24893—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including particulate material
- Y10T428/24901—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including particulate material including coloring matter
Definitions
- the present invention relates to an ultraviolet curable ink jet ink set and an outdoor coloring plate printed using the ink set. More specifically, an ultraviolet curable ink jet ink set that can be printed at a high density, can be obtained clearly, and has excellent color expression and weather resistance, and an outdoor use printed using the ink set. Concerning colored plates.
- ultraviolet curable resin has a merit that the resin is instantly cured when irradiated with ultraviolet rays, so that an ink receiving layer is not required for the recording substrate. Because of this merit, the use of the ultraviolet curable resin is not limited to coloring on paper, but its application as a coloring material to various materials such as film, plastic, metal and glass is being studied.
- the ultraviolet curable resin becomes a cured film excellent in scratching hardness and adhesion to the substrate
- the recorded matter can be used both outdoors and indoors.
- excellent weather resistance that can handle all natural conditions is required.
- the weather resistance is the resistance when exposed to heat, light, water, and the like.
- the recorded material must keep the printed image without discoloration or fading for a certain period of time, and the ink layer should not break or peel off from the substrate.
- UV curable resins are superior in weather resistance compared to other resins! /, But not enough! /.
- Japanese Patent Application Laid-Open No. 2001-55530 discloses a color printing method using an inorganic composite oxide pigment, which is excellent in light resistance and weather resistance and excellent in sharpness of hue.
- the inorganic pigment is inferior in coloring power compared to the organic pigment, so a high-density printed matter cannot be obtained.
- the inorganic composite oxide pigments used here tend to be light in strength and color because the crystal structure is destroyed when dispersed too much.
- yellow inorganic composite oxide pigments and blue inorganic composite oxide pigments have poor coloring power, so a large amount of pigment is required when trying to increase the color density, and is feasible as an inkjet ink. Absent. Therefore, it is difficult to increase the ink density substantially.
- the inorganic composite oxide does not have a bright red color, there are problems such as poor expression of intermediate colors from yellow to red, for example, orange, and intermediate colors from red to blue, for example, purple.
- the amount of pigment solids in the ink should be increased, but the amount of reactive monomer and / or reactive oligomer that can be blended is reduced, and ink is increased. It becomes sticky and discharge becomes difficult, and there is a risk of nozzle clogging. Therefore, there is a limit in increasing the amount of pigment solids for inkjet.
- an ultraviolet curable inkjet ink set that can be printed at a high density, is clear, and can provide a printed matter with excellent color expression and weather resistance has not been developed yet.
- the present invention provides an ultraviolet curable inkjet ink set that can be printed at a high density, can be obtained clearly, and has excellent color expression and weather resistance, and printing using the ink set.
- An object of the present invention is to provide an outdoor colored plate.
- the present invention provides a combination of a specific yellow pigment, red pigment, and blue pigment.
- the present invention is an ultraviolet curable inkjet ink set comprising a yellow ink, a magenta ink, and a cyan ink each containing a pigment, a reactive monomer and / or a reactive oligomer, and a photopolymerization initiator.
- the yellow ink contains at least a bismuth vanadate compound or iron oxide
- the magenta ink contains at least iron oxide or a condensed polycyclic compound
- the cyan ink contains at least a phthalocyanine compound.
- the present invention relates to an ink set.
- the pigment power contained in the yellow ink is C.I. 'Pigment Yellow 184 and / or C'I' Pigment Yellow 42, and the pigment contained in the magenta ink is SHI'I 'Pigment Red 101. , Si 'I' Pigment Red 102, C'I 'Pigment Tread 149, C.I. Pigment Red 168, C.I. Pigment Red 178, C.
- the average particle diameter of the pigment contained in the yellow ink is 50 to 200 nm
- the average particle diameter of the pigment contained in the magenta ink is 30 to 300 nm
- the average particle diameter of the pigment contained in the cyan ink Is preferably 50 to 150 nm.
- the pigment strength is preferably contained in each ink in an amount of 0 .;
- the present invention also relates to an outdoor ultraviolet curable inkjet ink set comprising the ultraviolet curable inkjet ink set described above.
- the present invention relates to an outdoor coloring plate printed using the ultraviolet curable ink jet ink set described above. Brief Description of Drawings
- FIG. 1 is a view showing a colored pattern printed on a brick pattern by ejecting ink onto a metal plate using the ink set of the present invention.
- the ultraviolet curable ink jet ink set composed of the yellow ink, the magenta ink, and the cyan ink of the present invention uses a specific pigment as a pigment of each ink.
- the yellow ink contains at least a bismuth vanadate compound or iron oxide as a yellow inorganic pigment.
- a bismuth vanadate compound C'I 'Pigment Yellow 184 is preferable.
- the iron oxide is preferably C'Iigment Yellow 42.
- 184 'I' pigment yellows are particularly preferred because of their strong coloring and vivid yellow color!
- the average particle size of the bismuth vanadate compound or iron oxide is preferably in the range of 50 to 200 nm, and is preferably 70 to 50 nm because vivid yellow ink and printed matter can be obtained. More preferred.
- the average particle size is 50 nm / J or more, the coloring power tends to be weak, and when it exceeds 200 nm, the discharge from the nozzle tends to be difficult. This is because inorganic pigments tend to settle due to their large density.
- the magenta ink contains at least iron oxide or a condensed polycyclic compound as a red pigment.
- the iron oxide C'I 'Pigment Red 101 and C'I' Pigment Red 102 are preferable.
- the condensed polycyclic compound has a coloring power and is clear, and C.I. Pigment Red 149, C.I. Pigment Red 168, S. I. Pigment Red 178, S.I. I. Pigment Red 179, S. I. 'Imagment Red 190, S. I.' I 'Pigment Red 224, S.' I '' Pigment Red 242, C '' I. • Pigment Red 254, C. I. Pigment Red 255, Sea Eye Pigment Red 270 And C.I. Pigment Red 272 are preferred.
- the average particle diameter of the iron oxide is preferably in the range of 50 to 300 nm, more preferably 70 to 200 nm, in order to obtain vivid magenta ink and printed matter. .
- the average particle size is less than 50 nm, yellowing tends to become strong and orange, and when it exceeds 300 nm, blue tends to become strong and purple. Dispensing tends to be difficult.
- the condensed polycyclic compound is an organic pigment, but forms a crystal structure in which molecules overlap each other, and is stable as a macromolecule through hydrogen bonding between multiple molecules of the pigment. It is the most excellent in light resistance, and it is difficult to fade even when used outdoors! /, A pigment.
- the average particle size of the condensed polycyclic compound is preferably 30 to 200 nm, more preferably 50 to 150 nm! /. When the average particle size is smaller than 30 nm, the weather resistance tends to be weak, and when it is larger than 200 nm, it tends to be difficult to eject from the nozzle.
- the cyan ink contains at least a phthalocyanine compound as a blue pigment.
- Phthalocyanine compounds are organic pigments, but have a structure in which a metal atom is coordinated to the center of the molecule, and because the phthalocyanine molecule is stabilized as a crystal by intermolecular forces between multiple molecules, it is an organic pigment. Among them, it is the most excellent in light resistance and is a pigment that hardly fades even when used outdoors.
- Examples of the phthalocyanine compounds include C'I 'Pigment Benoley 15, C'I' Pigment Blue 15: 1, C'I 'Pigment Blue 15: 2, C. I. Pigment Blue 15 : 3 , C. It is preferably at least one selected from eye pigment blue is : 4 , sea eye pigment blue 15: 6 and sea eye pigment blue 16.
- SHI'I 'Pigment Blue 15: 3 and SHI'I Pigment Blue 15: 4 Power S are particularly preferred because of their excellent light resistance.
- the average particle size of the phthalocyanine compound is excellent in saturation, good weather resistance, and can be used in combination with an inorganic pigment to obtain an ink and printed matter that are well balanced in light resistance. It is more preferable that it is 60-120 nm. When the average particle size is smaller than 50 nm, the weather resistance tends to be weakened, and when larger than 150 nm, ejection from the nozzle tends to be difficult.
- black inorganic pigments such as carbon black (C.I. Pigment Black 7) and white inorganic pigments such as titanium oxide (C.I. Pigment White 6) can be converted into ink and used together.
- black inorganic pigments such as carbon black (C.I. Pigment Black 7)
- white inorganic pigments such as titanium oxide (C.I. Pigment White 6)
- the pigment is preferably contained in each ink in an amount of 0.5;! To 10 wt%, more preferably 0.5 to 5 wt%. If the pigment content is less than 0.1% by weight, the ink concentration tends to be insufficient, and if it exceeds 10% by weight, ejection from the nozzle tends to be difficult.
- the weather resistance of the pigment means, in particular, resistance to sunlight (light resistance), and means that it hardly fades after being exposed outdoors for 5 to 10 years. For example, it can be confirmed in a short period of time using a testing machine such as a sunshine weather meter, metal weather or Super UV.
- the ink used in the present invention contains, in addition to the pigment, a reactive monomer and / or a reactive oligomer and a photopolymerization initiator.
- the reactive monomer and the reactive oligomer are not particularly limited, but are a so-called ultraviolet spring curable resin that is cured by irradiation with ultraviolet rays.
- reactive monomers include hexafunctional acrylates such as dipentaerythritol hexaatalylate and modified products thereof; pentafunctional acrylates such as dipentaerythritol hydroxypentaacrylate; pentaditrimethylolpropane tetraacrylate, pentaerythritol Tetrafunctional arylates such as tetraatarylate; Trifunctional acrylates such as trimethylolpropane tritalylate, pentaerythritol tritalylate, tris (2-hydroxyethyl) isocyanurate tritalylate, glyceryl tritalylate; hydroxy Vivalin acid neopentyl glycol ditalylate, polytetramethylene glycol d
- hydrocarbon reactive monomers such as 1,6-hexanediol diatalylate, neopentylglycol diatalylate, 1,3-butane are hydrocarbon reactive monomers that are hardly yellowed. Diol diatalylate, 1,4-butanediol diatalate, 1,9-nonanediol diatalate, and the like are preferable.
- the reactive monomer is preferably contained in the ink in an amount of 50 to 85% by weight. If the amount is less than 50% by weight, the viscosity of the ink becomes high, which may result in ejection failure. If the amount exceeds 85% by weight, other chemicals necessary for curing may be insufficient, leading to poor curing.
- Examples of the reactive oligomer include urethane acrylate, polyester acrylate, epoxy acrylate, silicon acrylate, and polybutadiene acrylate, which may be used alone or in combination.
- urethane acrylate is preferred because it is excellent in toughness, flexibility and adhesion.
- aliphatic urethane acrylates composed of hydrocarbons are more preferable in that they are hardly yellowed like reactive monomers.
- the reactive oligomer is preferably contained in the ink in an amount of 1 to 40% by weight, more preferably 5 to 40% by weight, and even more preferably 10 to 30% by weight. If the reactive oligomer is 1 to 40% by weight, the toughness, flexibility and adhesion tend to be further improved.
- Examples of the photopolymerization initiator include benzoins, benzyl ketals, amino ketones, titanocenes, bisimidazoles, hydroxy ketones, and acyl phosphine oxides, which may be used alone or in combination. good. Of these, hydroxy ketones and acyl phosphine oxides are preferred because they are highly reactive and hardly yellow.
- the addition amount of the photopolymerization initiator is preferably 1 to 10% by weight in the ink, more preferably 3 to 7% by weight. If the amount is less than 1% by weight, the polymerization may be incomplete and the film may be uncured. If the amount exceeds 10% by weight, no further increase in the curing rate and efficiency of the curing speed can be expected, resulting in high costs.
- a dispersant may be added to the ink used in the present invention, if necessary.
- Examples of the dispersant include a canyon surfactant, a cationic surfactant, and a noion interface. Examples thereof include an activator, a zwitterionic surfactant, and a polymer dispersant, and these can be used alone or in combination.
- the amount of the dispersant added to the ink is appropriately determined depending on the type of pigment to be dispersed, but it is preferably 5 to 150 parts by weight with respect to 100 parts by weight of the pigment. More preferably, it is 80 parts by weight. If the amount of the dispersant is less than 5 parts by weight, the pigment tends not to be dispersed well. If the amount exceeds 150 parts by weight, the dispersant tends to inhibit the pigment dispersion or increase the ink cost.
- a sensitizer if necessary, a heat stabilizer, an antioxidant, an antiseptic, an antifoaming agent, a penetrant, a resin binder, a resin emulsion, and a photopolymerization initiator.
- Additives such as anti-reversion agents, leveling agents, pH adjusters, pigment derivatives, polymerization inhibitors, UV absorbers and light stabilizers can also be added.
- the materials to be used are mixed, and the mixture is further dispersed using a disperser such as a roll mill, a ball mill, a colloid minole, a die mill or a bead mill, and then filtered.
- a disperser such as a roll mill, a ball mill, a colloid minole, a die mill or a bead mill, and then filtered.
- a bead mill is preferable because it can disperse in a large amount in a short time.
- the viscosity of the ink is preferably 2 to 20 mPa's at 50 ° C, more preferably 2 to 15 mPa's. If the viscosity is lower than ImPa's, there is a risk that the discharge amount will be too large due to the ink viscosity being too low.If it exceeds 20 mPa's, the ink viscosity will be too high. There is a possibility that it cannot be discharged.
- the surface tension at the time of discharge is preferably 20-40 dyne / cm, more preferably 25-35 dyne / cm, considering that it corresponds to various materials. If it is less than 20 dy ne / cm, the wettability will be too good and the image will tend to bleed, and it will be difficult to supply ink to the printer head. If it exceeds 40 dyne / cm, the wettability deteriorates, so that the ink is repelled and the image power S tends to be steep.
- the ink jet recording apparatus using the ink set of the present invention is not particularly limited.
- continuous methods such as charge modulation method, micro dot method, charge jet control method and ink mist method
- on-demand method such as stemme method, nozzleless jet method, bubble jet (registered trademark) method and electrostatic suction method Can be adopted is there.
- a head equipped in these ordinary ink jet printers may be equipped with a heating device, and the viscosity may be lowered by heating to discharge.
- the heating temperature is 25 to 150 ° C, preferably 30 to 70 ° C.
- the heating temperature is determined in consideration of the curing property of the reactive monomer and / or reactive oligomer to be used with respect to heat, and the heating temperature is set lower than the temperature at which curing starts by heat.
- the output of the ultraviolet lamp is preferably 50 to 280 W / cm, more preferably 80 to 200 W / cm force S. If the output of the UV fountain lamp is lower than 50 W / cm, the ink will not be cured sufficiently due to the peak intensity of UV light and insufficient accumulated light quantity. Or, it tends to melt and the cured film of the ink deteriorates.
- the irradiation time of ultraviolet rays is preferably 0.;! To 20 seconds, more preferably 0.5 to 10 seconds.
- the irradiation time of the ultraviolet lamp is longer than 20 seconds! /, And the substrate tends to be deformed or melted by the heat of the ultraviolet lamp, and the cured film of the ultraviolet curable ink tends to deteriorate. If it is short, the accumulated amount of UV light is insufficient, and the UV curable ink tends not to be cured sufficiently.
- the amount of ink discharged onto the substrate is preferably !!-200 g / m 2 . 5 ⁇ 150g / m
- the ink set of the present invention is extremely excellent in weather resistance, exterior materials such as exterior walls of buildings, roofing materials, pillars and doors, exterior materials such as gates, fences and entrance approaches, signboards, signs, etc. It is possible to use it for anything that is used outdoors.
- the outdoor coloring plate having an ink layer of the ink set of the present invention has almost no fading even when used outdoors because the ink layer has weather resistance. Further, since the ink layer is made of ultraviolet curable ink, it has excellent adhesion to the substrate.
- the base material of the colored plate is not particularly limited. Plastics and ceramics , Glass, wood, metal, and those subjected to primer treatment. In particular, considering that it is used outdoors, it is preferable to be a metal and ceramics.
- the metals include, but are not limited to, ordinary steel plates, plated steel plates such as galvalume steel plates, steel plates such as coated steel plates and stainless steel plates, aluminum plates, and copper plates.
- PCM steel sheets in which various kinds of resin coats are applied to metals as an undercoat layer, such as metal siding materials can also be mentioned.
- the metal siding material may be uneven by embossing or drawing.
- the back side may be coated with a back side material such as aluminum laminated kraft paper, using an inorganic material such as resin foam or gypsum board as a core material to provide heat insulation and sound insulation.
- the ceramics are not particularly limited, and include unglazed porcelain plates (water-absorbing), glazed 'fired porcelain plates (non-absorbent), and cement plates.
- unglazed porcelain plates water-absorbing
- glazed 'fired porcelain plates non-absorbent
- cement plates cement plates
- ceramic siding materials those formed into a plate shape using cementitious raw materials and fibrous raw materials are also included. Further, the ceramic siding material may be provided with unevenness by embossing or the like.
- post-processing such as top coat or embossing can be performed on the printed matter, and there is no particular limitation.
- the thickness and shape of the base material are not particularly limited, and can be set as appropriate according to the application, use place, form, and the like.
- the thickness of the ink layer is preferably 5 to 150; If it is thinner than 111, it tends to be difficult to sufficiently color, and if it exceeds 150 111, the ink film thickness becomes too thick, and the printed layer tends to crack or peel off.
- the ink layer may be applied to the substrate using the above-described ink jet recording apparatus!
- the colored pattern include a brick pattern, a tile pattern, and a wood grain pattern.
- the brick pattern is a pattern in which a plurality of bricks 10 are stacked and a boundary region 20 is formed.
- the applied ink layer is excellent in adhesion to the substrate, it is difficult to peel off even if embossing or bending is performed as post-processing.
- Sicopal Yellow L1100 C'I Pigment Yellow 184, bismuth nonadimate, manufactured by BASF Japan Ltd.
- dispersant Dispersant (Disperbyk-168, polymer dispersant, manufactured by BykChemie) 3 parts by weight, 20 parts by weight of reactive oligomer (CN985B88, aliphatic urethane acrylate, bifunctional, manufactured by Sartomer Co., Ltd.), reactive monomer (SR238F, 1,6 hexanediol ditalylate, 2 69 parts by weight of organoleptic, manufactured by Sartoma Co., Ltd.), and photopolymerization initiator (Irgacure 2959, 1- [4- (2 hydroxyethyl) phenenole] 2-hydroxy 2-methynole 1 propane 1 1 on, Ciba ⁇ 5 parts by weight of Specialty Chemicals Co., Ltd.) was added and dispersed using a bead mill dis
- a magenta ink was prepared in the same manner as the yellow ink except that 130ED (C'I Pigment Red 101, iron oxide, manufactured by Toda Kogyo Co., Ltd.) was used as the inorganic pigment.
- the average particle size of the pigment used was 151 nm.
- a cyan ink was prepared in the same manner as the yellow ink, except that IRGALITE Blue GLVO (C'I Pigment Blue 15: 4, Copper Phthalocyanine, Ciba Specialty Chemikanorezu Co., Ltd.) was used as the organic pigment.
- the average particle size of the pigment used was 65 nm.
- the amount of ink discharged onto the substrate was 20 g / m 2 , respectively.
- Evaluation pattern 2 Select two inks from yellow, magenta, and cyan inks, and use the ratio shown in Table 1 (the intermediate colors (5 to 95) increase or decrease the ink amounts of the two colors in increments of 5 to make a total of 100).
- the total ink discharge amount to the substrate was 20 g / m 2 .
- the matrix pattern printed here is a pattern in which regions colored in squares are arranged in a horizontal row in contact with each other. For example, when yellow ink and magenta ink are used, 21 squares are arranged, and the color gradually changes from yellow to orange to red from left to right.
- FIG. 1 is an explanatory diagram of a brick pattern printed by ejecting ink onto a substrate using the ink set of the present invention.
- the brick pattern is a pattern in which a plurality of bricks 10 are stacked and a boundary region 20 is formed.
- the color density of the evaluation pattern 1 was measured with a reflection densitometer (Macbeth RD918). The results are shown in Table 2. The higher the value, the higher the concentration.
- the color expression of the evaluation pattern 2 was evaluated before and after the weather resistance test.
- the weathering test conditions are as follows.
- the saturation C * and the hue angle h were measured for the intermediate color (50) portion in which the ejection amount ratio of the two colors of ink was 50:50. Saturation and hue angle were measured before and after the weathering test, and measured with a spectrocolorimeter (CM-3600d, manufactured by Konica Minolta Sensing Co., Ltd.) using the L * C * h color system. The results are shown in Table 3.
- the L * C * h color system is based on the L * a color system (JIS Z 8729), where L * is lightness, C * is saturation, and h is hue angle.
- L * is lightness
- C * is saturation
- h hue angle.
- h is the angle moved with respect to the hue in the counterclockwise direction with the axis of the a * red direction as 0 ° and the axis as the reference. .
- h When h is 0 °, it shows red, 90 ° shows yellow, 180 ° shows green, and 270 ° shows blue.
- C * aV color system chromaticity diagram when C * is a larger value, it becomes more vivid, and when C * is a smaller value, it becomes a duller color. Means that.
- Table 4 shows values obtained by subtracting the saturation and hue angle before the weather test from the saturation and hue angle after the weather test.
- the hardness of the colored plate was confirmed before and after the weathering test.
- a pencil was used, the angle between the colored plate and the pencil was 45 °, and the load was 1 kg.
- the evaluation was based on the hardness of the printed layer, which is one less than the lead brush hardness from which the printed layer was peeled off. The results are shown in Table 5.
- the adhesion of the colored plate before and after the weather resistance test was confirmed.
- the adhesion test was performed using a cutter knife and drawing lines that reached the substrate at 11 mm intervals in the vertical and horizontal directions to make 100 grids.
- cellophane tape was applied on the grid, and the cellophane tape was quickly removed to check the condition of the colored plate.
- the evaluation was based on the following four levels according to the contents of JIS K5600-5-6. The results are shown in Table 5.
- Print layer peels along the edge of the cut and / or at the intersection 3 ⁇ ⁇
- the print layer is partially or totally peeled along the edge of the cut and / or various partial forces are partially or totally peeled off.
- the print layer is partially or totally peeled along the edges of the cut, and / or some eyes are partially or completely peeled off.
- a yellow ink was prepared in the same manner as in Example 1 except that Sicotrans Yellow L1916 (C'I Pigment Yellow 42, iron oxide, manufactured by BASF Japan Ltd.) was used as the inorganic pigment.
- the average particle size of the pigment used was 75 nm.
- a magenta ink was produced in the same manner as in Example 1 except that IRGAZIN Red 179 (C'I Pigment Red 179, condensed polycyclic compound, manufactured by Ciba Specialty Chemicals Co., Ltd.) was used as the organic pigment.
- the average particle size of the pigment used was 54 nm.
- a cyan ink was prepared in the same manner as in Example 1 except that IRGALITE Blue GLO (Ci Pigment Blue 15: 3, copper phthalocyanine, Ciba Specialty Chemicals Co., Ltd.) was used as the organic pigment. .
- the average particle size of the pigment used was 139 nm.
- Example 1 The ink obtained in Example 1 was used as an ink set, and printing was performed in the same manner as in Example 1 except for the amount of ink discharged to the base material to obtain a printed matter.
- the discharge amount of each ink in the evaluation pattern 1 was 50 g / m 2 .
- the total ink discharge amount for the evaluation patterns 2 and 3 was 50 g / m 2 .
- the obtained printed matter was evaluated in the same manner as in Example 1. The results are shown in Tables 2-5.
- Sicopal Yellow L1100 (C'I 'Pigment Yellow 184, 0.5 parts by weight of bismuth nadimate, manufactured by BASF Japan Ltd., 0.5 parts by weight of dispersant (Disperbyk—168, polymer dispersant, manufactured by BykChemie), reactive oligomer (CN98 5B88, 22 parts by weight of aliphatic urethane acrylate, bifunctional, manufactured by Sartomer Co., Ltd., 72 weights of reactive monomer (SR238F, 1,6 hexanediol ditalylate, bifunctional, manufactured by Sartomer Co., Ltd.) And 5 parts by weight of a photopolymerization initiator (Irgacure 2959, 1- [4- (2 hydroxyethoxy) phenyl] 2-hydroxy-2-methyl-1-propane 1-one, manufactured by Ciba Specialty Chemicals Co., Ltd.) After dispersion using a bead mill disperser,
- a magenta ink was produced in the same manner as the yellow ink except that Paliogen Red L3910D (Shi'I 'Pigment Red 178, condensed polycyclic compound, manufactured by BASF Japan Ltd.) was used as the organic pigment.
- the average particle size of the pigment used was 151 nm.
- a cyan ink was prepared in the same manner as the yellow ink, except that IRGALITE Blue GLVO (C'I Pigment Blue 15: 4, Copper Phthalocyanine, Ciba Specialty Chemikanorezu Co., Ltd.) was used as the organic pigment.
- the average particle size of the pigment used was 65 nm.
- Example 2 Using the obtained ink as an ink set, except for the amount of ink discharged to the substrate, Example
- Example 4 The ink obtained in Example 4 was used as an ink set, and printing was performed in the same manner as in Example 1 except for the amount of ink discharged to the base material to obtain a printed matter.
- the discharge amount of each ink in the evaluation pattern 1 was 190 g / m 2 .
- the total ink discharge amount for the evaluation patterns 2 and 3 was 190 g / m 2 .
- the obtained printed matter was evaluated in the same manner as in Example 1. The results are shown in Tables 2-5. [0094] Example 6
- Sicopal Yellow L1100 (C'I Pigment Yellow 184, bismuth nonadium acid, manufactured by BASF Japan Ltd.) 8 parts by weight, dispersant (Disperbyk-168, polymer dispersant, manufactured by BykChemie) 8 parts by weight, reactive oligomer (CN985B88, aliphatic urethane acrylate, bifunctional, manufactured by Sartomer Co., Ltd.), 15 parts by weight, reactive monomer (SR238F, 1,6 hexanediol diatalylate, 2 64 parts by weight of organoleptic, manufactured by Sartoma Co., Ltd.), and photopolymerization initiator (Irgacure 2959, 1- [4- (2 hydroxyethyl) phenenole] 2-hydroxy 2-methynole 1 propane 1 1 on, Ciba ⁇ 5 parts by weight of Specialty Chemicals Co., Ltd.) was added and dispersed using a bead mill disperser
- a magenta ink was prepared in the same manner as the yellow ink except that PV FAST RED B (C'I Pigment Red 149, condensed polycyclic compound, manufactured by Clariant Japan Co., Ltd.) was used as the organic pigment.
- the average particle size of the pigment used was 151 nm.
- a cyan ink was prepared in the same manner as the yellow ink, except that IRGALITE Blue GLVO (C'I Pigment Blue 15: 4, Copper Phthalocyanine, Ciba Specialty Chemikanorezu Co., Ltd.) was used as the organic pigment.
- the average particle size of the pigment used was 65 nm.
- Organic Pigment PV Fast Yellw H2G (Shiichi 'I' Pigment Yellow 120, Benzimi Yellow ink was prepared in the same manner as in Example 1 except that Dazolone (manufactured by Clariant Japan Co., Ltd.) was used.
- the average particle size of the pigment used was 92 nm.
- a magenta ink was produced in the same manner as in Example 1.
- a cyan ink was produced in the same manner as in Example 1.
- a yellow ink was prepared in the same manner as in Example 1.
- a magenta ink was prepared in the same manner as in Example 1 except that the organic pigment Graphtol Rubine L6B (Shi'I 'Pigment Red 57: 1, Ca Lake, Clariant Japan Co., Ltd.) was used.
- the average particle size of the pigment used was 15 lnm.
- a cyan ink was produced in the same manner as in Example 1.
- a yellow ink was prepared in the same manner as in Example 1.
- a magenta ink was produced in the same manner as in Example 1.
- a cyan ink was prepared in the same manner as in Example 1 except that PTM lake (manufactured by BASF Japan Ltd.) was used. The average particle size of the pigment used was 52 nm. [0109] Using the obtained ink as an ink set, printing was performed in the same manner as in Example 1, and the obtained printed matter was evaluated. The results are shown in Tables 2-5.
- inorganic pigment Sicotan Yellow L1010 C. L Pigment Yellow 53, composite oxide, manufactured by BASF Japan Ltd.
- dispersant HPD-96 polymer dispersant, solid content 34%
- Johnson polymer 5 parts by weight
- Binder Jonkrill 741 solid content 49%, manufactured by Johnson Polymer Co., Ltd.
- wetting agent propylene glycol manufactured by Showa Denki Co., Ltd.
- Wetting agent Add 1 part by weight of urea (Mitsui Chemicals Co., Ltd.) and 78 parts by weight of pure water, disperse using a bead mill disperser, filter to remove impurities, and produce a uniform yellow ink. did.
- the average particle size of the pigment used was 135 nm.
- a magenta ink was prepared in the same manner as the yellow ink except that the inorganic pigment DAIPYROXIDE BROWN 9220 (C.I. Pigment Brown 22, Compound Oxide, Dainichi Seika Kogyo Co., Ltd.) was used.
- the average particle size of the pigment used was 94 nm.
- a cyan ink was prepared in the same manner as the yellow ink except that the inorganic pigment DAIPYROXIDE BLUE 9410 (CL Pigment Blue 28, composite oxide, Dainichi Seika Kogyo Co., Ltd.) was used.
- the average particle size of the pigment used was 88 nm.
- the printed materials (Examples ;! to 6) obtained using the ink set of the present invention are yellow to red, red to blue, and blue to yellow. All color gamuts express a clear gradation of colors in a well-balanced manner. It can be seen that the color expression does not deteriorate even after the weather resistance test. On the other hand, comparative example ; To 3 have undergone a weather resistance test, resulting in deterioration of color expression.
- Table 4 shows values obtained by subtracting the saturation and hue angle before the weather test from the saturation and hue angle after the weather test based on the description in Table 3, respectively. From Table 4, it is possible to know the changes in saturation and hue angle due to the print being subjected to the weather resistance test.
- the printed matter (Examples 1 to 6) obtained using the ink set of the present invention is excellent in light resistance with almost no color change due to a weather resistance test.
- Comparative Examples 1 to 3 have a large color change and inferior light resistance. After passing through the weathering test, in Examples;! To 5, there is no change in hardness and adhesion, but in Comparative Example 4, the hardness and adhesion are reduced! /.
- a printed matter that can be printed at a high density is clear, and has excellent color expression, in particular, color expression of yellow to red, red to blue and blue to yellow, and excellent weather resistance.
- An ink set that can be provided can be provided.
Description
Claims
Priority Applications (3)
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JP2008536322A JP5210169B2 (ja) | 2006-09-27 | 2007-09-10 | 紫外線硬化型インクジェット用インクセットおよび該インクセットを使用して印刷した屋外用着色板 |
US12/443,193 US8642163B2 (en) | 2006-09-27 | 2007-09-10 | Ultraviolet-curable inkjet ink set and colored board for outdoor use printed by using the ink set |
CA 2664923 CA2664923A1 (en) | 2006-09-27 | 2007-09-10 | Ultraviolet-curable inkjet ink set and colored board for outdoor use printed by using the ink set |
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JP2006262828 | 2006-09-27 | ||
JP2006-262828 | 2006-09-27 |
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WO2008038508A1 true WO2008038508A1 (fr) | 2008-04-03 |
Family
ID=39229947
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PCT/JP2007/067580 WO2008038508A1 (fr) | 2006-09-27 | 2007-09-10 | Ensemble d'encres pour impression jet d'encre durcissables par ultraviolet et plaque colorée pour une utilisation à l'extérieur imprimée à l'aide dudit ensemble d'encres |
Country Status (4)
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US (1) | US8642163B2 (ja) |
JP (1) | JP5210169B2 (ja) |
CA (1) | CA2664923A1 (ja) |
WO (1) | WO2008038508A1 (ja) |
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JP2009249631A (ja) * | 2008-04-10 | 2009-10-29 | Xerox Corp | 硬化性オーバーコート組成物 |
EP2230285A1 (en) * | 2009-03-19 | 2010-09-22 | Fujifilm Corporation | Ink composition, inkjet recording method, printed material, and process for producing molded printed material |
US20120164402A1 (en) * | 2010-04-27 | 2012-06-28 | Seiren Co., Ltd. | Decorative concrete block and method of manufacturing decorative concrete block |
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WO2013146722A1 (ja) * | 2012-03-28 | 2013-10-03 | 富士フイルム株式会社 | 活性光線硬化型インクジェットインク組成物及びその製造方法、インクジェット記録方法、並びに、印刷物 |
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JP2014065862A (ja) * | 2012-09-27 | 2014-04-17 | Dainippon Toryo Co Ltd | 活性エネルギー線硬化型インクジェットインク組成物、レンズ状粒子の形成方法及び複合材料 |
JP2014129481A (ja) * | 2012-12-28 | 2014-07-10 | Dainippon Toryo Co Ltd | 活性エネルギー線硬化型インクセット及び建築板 |
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- 2007-09-10 JP JP2008536322A patent/JP5210169B2/ja not_active Expired - Fee Related
- 2007-09-10 WO PCT/JP2007/067580 patent/WO2008038508A1/ja active Application Filing
- 2007-09-10 CA CA 2664923 patent/CA2664923A1/en not_active Abandoned
- 2007-09-10 US US12/443,193 patent/US8642163B2/en not_active Expired - Fee Related
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JPH1112512A (ja) * | 1997-06-20 | 1999-01-19 | Toyo Ink Mfg Co Ltd | インクジェット用記録液 |
JP2003342503A (ja) * | 2002-05-28 | 2003-12-03 | Konica Minolta Holdings Inc | インクジェット記録用ブラックインクおよび画像形成方法 |
JP2004018546A (ja) * | 2002-06-12 | 2004-01-22 | Konica Minolta Holdings Inc | インクジェット用インクセット及びインクジェット画像形成方法 |
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Also Published As
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JP5210169B2 (ja) | 2013-06-12 |
US8642163B2 (en) | 2014-02-04 |
US20100092736A1 (en) | 2010-04-15 |
CA2664923A1 (en) | 2008-04-03 |
JPWO2008038508A1 (ja) | 2010-01-28 |
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