WO2022138142A1 - 画像記録方法及びインクジェット記録物 - Google Patents
画像記録方法及びインクジェット記録物 Download PDFInfo
- Publication number
- WO2022138142A1 WO2022138142A1 PCT/JP2021/044946 JP2021044946W WO2022138142A1 WO 2022138142 A1 WO2022138142 A1 WO 2022138142A1 JP 2021044946 W JP2021044946 W JP 2021044946W WO 2022138142 A1 WO2022138142 A1 WO 2022138142A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ink
- liquid crystal
- image recording
- types
- recording method
- Prior art date
Links
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Classifications
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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
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- B42D—BOOKS; BOOK COVERS; LOOSE LEAVES; PRINTED MATTER CHARACTERISED BY IDENTIFICATION OR SECURITY FEATURES; PRINTED MATTER OF SPECIAL FORMAT OR STYLE NOT OTHERWISE PROVIDED FOR; DEVICES FOR USE THEREWITH AND NOT OTHERWISE PROVIDED FOR; MOVABLE-STRIP WRITING OR READING APPARATUS
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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
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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
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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
Definitions
- This disclosure relates to an image recording method and an inkjet recorded material.
- the cholesteric liquid crystal produced by adding a chiral agent to a liquid crystal compound has a peculiar light reflectivity, and has a characteristic that the color tone changes depending on the viewing angle.
- an ink containing a liquid crystal compound is used, a special image not found in other image recording materials can be recorded, so that it can be expected to be applied to special decoration for articles such as packaging materials and security printing.
- a base layer forming step of applying a base ink onto a base material by an inkjet recording method to form a base layer, and an image recording ink containing a polymerizable liquid crystal compound and a chiral compound are provided.
- an image recording method including an image recording step of recording an ink image by applying the ink jet to the base layer by an inkjet recording method.
- the disclosure includes the following aspects: ⁇ 1> A step of preparing at least two kinds of inks including the first ink and a second kind of ink, a step of heating the base material, and a step of heating at least two kinds of inks on the heated base material using an inkjet recording method.
- the step of applying at least two types of ink which includes a step of irradiating at least two types of ink with active energy rays, at least a part of the substrate is at least 2 by applying.
- An image recording method comprising a mixed region in which seed inks are mixed, the first ink containing a first polymerizable liquid crystal compound, and the second ink containing a second chiral compound.
- the first ink contains a first polymerizable liquid crystal compound, a first chiral compound, and a first organic solvent
- the second ink includes a second polymerizable liquid crystal compound, a second chiral compound, and a second organic solvent.
- the absolute value of the difference between the maximum reflection wavelength of the ink film formed by the first ink and the maximum reflection wavelength of the ink film formed by the second ink is 100 nm or more, according to ⁇ 1>. Image recording method.
- the maximum reflection wavelength of the ink film formed by the first ink is 380 nm to 490 nm, and the maximum reflection wavelength of the ink film formed by the second ink is 600 nm to 800 nm, ⁇ 1> or ⁇ 2>.
- the image recording method described in. ⁇ 4> In the step of preparing at least two kinds of inks, a third ink containing a third polymerizable liquid crystal compound, a third chiral compound, and a third organic solvent is further prepared, and an ink film formed by the first ink.
- the absolute value of the difference between the maximum reflection wavelength of the ink film and the maximum reflection wavelength of the ink film formed by the second ink and the maximum reflection wavelength of the ink film formed by the third ink is 40 nm or more, ⁇ 1.
- the image recording method according to any one of ⁇ 3>. ⁇ 5> The maximum reflection wavelength of the ink film formed by the first ink is 380 nm to 490 nm, the maximum reflection wavelength of the ink film formed by the second ink is 600 nm to 800 nm, and the ink film is formed by the third ink.
- the total amount of at least two types of ink applied per unit area is applied in the range of 3 g / m 2 to 20 g / m 2 in the mixed region, ⁇ 1>.
- ⁇ 7> In the step of applying at least two types of ink, the total amount of the polymerizable liquid crystal compound contained in at least two types of ink per unit area is 1.5 g / m 2 to 8 g / m 2 in the mixed region.
- the total amount of the organic solvent contained in at least two types of ink per unit area is 2.5 g / m 2 to 12.5 g / m 2 in the mixed region.
- the image recording method according to any one of ⁇ 2> to ⁇ 7>, which is given as the range of. ⁇ 9> The image recording method according to any one of ⁇ 1> to ⁇ 8>, wherein each of at least two types of ink has a viscosity of 7 mPa ⁇ s or more.
- ⁇ 10> The image recording according to any one of ⁇ 1> to ⁇ 9>, wherein at least two types of ink have a maximum value of 1 mN / m or less among the absolute values of the difference in surface tension between the inks.
- Method. ⁇ 11> The image recording method according to any one of ⁇ 1> to ⁇ 10>, wherein the base material is heated to 40 ° C. or higher in the step of heating the base material.
- a base material and an ink film containing a liquid crystal polymer provided on the base material are provided, and the ink film includes a plurality of regions having different maximum reflection wavelengths in a plan view and is adjacent to each other. Inkjet recordings in which the orientation of the liquid crystal polymer changes continuously between the two regions.
- an image recording method and an inkjet recorded material capable of reproducing various colors with high color development.
- the numerical range indicated by using "-" in the present specification means a range including the numerical values before and after "-" as the minimum value and the maximum value, respectively.
- the upper limit value or the lower limit value described in one numerical range may be replaced with the upper limit value or the lower limit value of the numerical range described in another stepwise description.
- the upper limit value or the lower limit value described in a certain numerical range may be replaced with the value shown in the examples.
- the amount of each component in the composition is the total amount of the plurality of substances present in the composition unless otherwise specified, when a plurality of substances corresponding to each component are present in the composition. Means. Further, in the present specification, a combination of two or more preferred embodiments is a more preferred embodiment. Further, in the present specification, the term “process” is used not only as an independent process but also as long as the intended purpose of the process is achieved even if it cannot be clearly distinguished from other processes. include. As used herein, "(meth) acrylate” means acrylate or methacrylate.
- the image recording method of the present disclosure includes a step of preparing at least two kinds of inks including a first ink and a second kind of ink, a step of heating a base material, and a step of heating at least two kinds of inks on the heated base material.
- the step of applying at least two types of ink including the step of applying using an inkjet recording method and the step of irradiating at least two types of ink with active energy rays, at least a part of the substrate is used.
- the first ink contains a first polymerizable liquid crystal compound
- the second ink contains a second chiral compound to obtain various colors. It can be reproduced with high color development.
- an ink image can be recorded by applying ink on a base material.
- An ink image is a cured product of ink.
- a mixed region in which at least two types of ink are mixed is formed by applying at least a part of the substrate. Since the first ink contains the first polymerizable liquid crystal compound and the second ink contains the second chiral compound, the first polymerizable liquid crystal compound and the second chiral compound are mixed, and the first polymerizable liquid crystal compound is mixed. Formes a helical structure with a second chiral compound to form a cholesteric liquid crystal.
- the ink image in the present disclosure expresses the structural color. Further, by controlling the amount of the first ink to be dropped and the amount of the second ink to be dropped, the first polymerizable liquid crystal compound contained in the first ink and the second ink contained in the second ink in the mixing region. The mixing ratio with the chiral compound can be adjusted. Therefore, it is possible to reproduce various colors by forming a mixed region in which at least two kinds of inks are mixed.
- the image recording method of the present disclosure by applying at least two kinds of inks on the heated substrate by using an inkjet recording method, a mixed region in which at least two kinds of inks are mixed is formed.
- the mixed region is difficult to expand. Therefore, the polymerizable liquid crystal compound can be uniformly oriented by the chiral compound, and it is possible to reproduce a color having high color development.
- the image recording method of the present disclosure includes a step of preparing at least two kinds of inks including the first ink and the second ink (hereinafter, also referred to as "ink preparation step").
- the first ink contains a first polymerizable liquid crystal compound
- the second ink contains a second chiral compound. That is, at least two kinds of inks contain a polymerizable liquid crystal compound and a chiral compound.
- the first ink may contain a component other than the first polymerizable liquid crystal compound. Further, the second ink may contain a component other than the second chiral compound.
- the combination of the first ink and the second ink in the image recording method of the present disclosure includes the following aspects. (1) A mode in which the first ink contains a first polymerizable liquid crystal compound, the second ink contains a second polymerizable liquid crystal compound and a second chiral compound (2) The first ink contains a first polymerizable liquid crystal compound and a first.
- the first ink contains a first polymerizable liquid crystal compound, a first chiral compound and a first organic solvent.
- the ink contains a second polymerizable liquid crystal compound and a second chiral compound (4)
- the first ink contains a first polymerizable liquid crystal compound, a first chiral compound and a first organic solvent, and the second ink is second polymerized.
- the first ink contains a first polymerizable liquid crystal compound and a first organic solvent
- the second ink is a second chiral compound and a second organic solvent.
- the first ink contains a first polymerizable liquid crystal compound, a first chiral compound, and a first organic solvent
- the second ink is a second polymerizable liquid crystal compound, a second.
- the absolute value of the difference between the maximum reflection wavelength of the ink film formed by the first ink and the maximum reflection wavelength of the ink film formed by the second ink, which contains the chiral compound and the second organic solvent is 100 nm or more. It is preferable to have.
- both the first ink and the second ink preferably contain a polymerizable liquid crystal compound, a chiral compound, and an organic solvent, and the ink film formed by the first ink and the ink film formed by the second ink. Is preferably a different hue.
- the first polymerizable liquid crystal compound and the second polymerizable liquid crystal compound may be the same or different.
- the first chiral compound and the second chiral compound may be the same or different.
- the first organic solvent and the second organic solvent may be the same or different.
- the hue difference is large and various colors are produced. It can be reproduced.
- the absolute value of the above difference is more preferably 130 nm or more, and further preferably 150 nm or more.
- the upper limit of the absolute value of the above difference is, for example, 400 nm.
- the polymerizable liquid crystal compound or the chiral compound By adjusting the content, the absolute value of the difference between the maximum reflection wavelength of the ink film formed by the first ink and the maximum reflection wavelength of the ink film formed by the second ink can be 100 nm or more. ..
- the maximum reflection wavelength of the ink film formed by the first ink is preferably 380 nm to 490 nm, and the maximum reflection wavelength of the ink film formed by the second ink. Is preferably 600 nm to 800 nm. Further, the maximum reflection wavelength of the ink film formed by the first ink is more preferably 390 nm to 420 nm, and the maximum reflection wavelength of the ink film formed by the second ink is more preferably 600 nm to 700 nm.
- the maximum reflection wavelength of the ink film is calculated by the following method. Ink is applied onto a transparent polyethylene terephthalate substrate under the condition of 100% halftone dot ratio, dried at 50 ° C. for 5 minutes, and further dried at 80 ° C. for 5 minutes to completely remove the organic solvent contained in the ink. .. Next, an ink film is obtained by curing with a metal halide lamp (product name "CSOT-40, manufactured by GS Yuasa). For the maximum reflection wavelength, this ink film is fluorescent spectrophotometer (product name" FD-7 ", Konica Minolta). It is calculated by measuring the spectral reflectance with (manufactured by the manufacturer).
- a black paper of hiding ratio measurement paper (standard: JIS K 5600 (ISO / FDIS 6504-3: 1998), manufactured by TP Giken) is placed under the base material so that the ink film becomes the outermost layer. Set to and measure the color.
- the third ink contains a third polymerizable liquid crystal compound, a third chiral compound, and a third organic solvent, has a maximum reflection wavelength of the ink film formed by the first ink, and an ink film formed by the second ink.
- the absolute value of the difference between the maximum reflection wavelength of the ink film and the maximum reflection wavelength of the ink film formed by the third ink is preferably 40 nm or more. In other words, the absolute value of the difference between the maximum reflection wavelength of the ink film formed by the first ink and the maximum reflection wavelength of the ink film formed by the third ink, and the ink film formed by the second ink.
- the absolute value of the difference between the maximum reflection wavelength and the maximum reflection wavelength of the ink film formed by the third ink is preferably 40 nm or more.
- the third polymerizable liquid crystal compound may be the same as or different from either the first polymerizable liquid crystal compound or the second polymerizable liquid crystal compound.
- the third chiral compound may be the same as or different from either the first chiral compound or the second chiral compound.
- the third organic solvent may be the same as or different from either the first organic solvent or the second organic solvent.
- the absolute value of the difference between the maximum reflection wavelength of the ink film formed by the first ink and the maximum reflection wavelength of the ink film formed by the second ink and the maximum reflection wavelength of the ink film formed by the third ink When is 40 nm or more, more various colors can be reproduced.
- the absolute value of the above difference is more preferably 50 nm or more, and further preferably 70 nm or more.
- the upper limit of the absolute value of the above difference is, for example, 150 nm.
- the first polymerizable liquid crystal compound, the second polymerizable liquid crystal compound, and the third polymerizable liquid crystal compound are the same, and the first chiral compound, the second chiral compound, and the third chiral compound are the same.
- the maximum reflection wavelength of the ink film formed by the first ink and the maximum reflection wavelength of the ink film formed by the second ink, and the first The absolute value of the difference from the maximum reflection wavelength of the ink film formed by the three inks can be 40 nm or more.
- the maximum reflection wavelength of the ink film formed by the first ink is preferably 380 nm to 490 nm, and the maximum reflection wavelength of the ink film formed by the second ink. Is preferably 600 nm to 800 nm, and the maximum reflection wavelength of the ink film formed by the third ink is preferably 500 nm to 590 nm. Further, the maximum reflection wavelength of the ink film formed by the first ink is more preferably 390 nm to 470 nm, and the maximum reflection wavelength of the ink film formed by the second ink is more preferably 600 nm to 700 nm. The maximum reflection wavelength of the ink film formed by the third ink is more preferably 500 nm to 550 nm.
- the polymerizable liquid crystal compound for example, the first polymerizable liquid crystal compound to the third polymerizable liquid crystal compound contained in at least two kinds of inks prepared in the ink preparation step will be described simply as “polymerizable liquid crystal compound”.
- the chiral compounds first chiral compound to third chiral compound contained in at least two kinds of inks prepared in the ink preparation step will be described simply as “chiral compounds”.
- the organic solvent for example, the first organic solvent to the third organic solvent contained in at least two kinds of inks prepared in the ink preparation step will be described simply as "organic solvent”. Further, at least two kinds of inks prepared in the ink preparation step will be described simply as "inks”.
- the polymerizable liquid crystal compound is a liquid crystal compound having a polymerizable group.
- the liquid crystal compound may be a rod-shaped liquid crystal compound or a disk-shaped liquid crystal compound, but is preferably a rod-shaped liquid crystal compound.
- Examples of the rod-shaped liquid crystal compound include a rod-shaped nematic liquid crystal compound.
- Examples of the rod-shaped nematic liquid crystal compound include azomethine compound, azoxy compound, cyanobiphenyl compound, cyanophenyl ester compound, benzoic acid ester, cyclohexanecarboxylic acid phenyl ester, cyanophenylcyclohexane compound, cyano-substituted phenylpyrimidin compound, alkoxy-substituted phenylpyrimidin compound, and phenyl.
- a dioxane compound, a trans compound or an alkenylcyclohexylbenzonitrile compound is preferably used.
- As the rod-shaped liquid crystal compound not only a small molecule liquid crystal compound but also a high molecular weight liquid crystal compound can be used.
- the polymerizable liquid crystal compound is obtained by introducing a polymerizable group into the liquid crystal compound.
- the polymerizable group include a polymerizable unsaturated group, an epoxy group and an aziridinyl group.
- the polymerizable group is preferably a polymerizable unsaturated group, and particularly preferably an ethylenically unsaturated group.
- the number of polymerizable groups contained in the polymerizable liquid crystal compound is preferably 1 to 6, and more preferably 1 to 3. From the viewpoint of the durability of the obtained image, it is more preferable that the polymerizable liquid crystal compound has two polymerizable groups in the molecule.
- polymerizable liquid crystal compound examples include Makromol. Chem. , 190, 2255 (1989), Advanced Materials 5, 107 (1993), US Pat. No. 4,683,327, US Pat. No. 5,622,648, US Pat. No. 5,770,107, International Publication No. 95/22586, International Publication No. 95/24455, International Publication No. 97/00600, International Publication No. 98/23580, International Publication No. 98/52905, Japanese Patent Application Laid-Open No. 1-272551, Japanese Patent Application Laid-Open No. 6- Examples thereof include the compounds described in Japanese Patent Application Laid-Open No. 16616, Japanese Patent Application Laid-Open No. 7-110469, Japanese Patent Application Laid-Open No. 11-80081, and Japanese Patent Application Laid-Open No. 2001-328973.
- polymerizable liquid crystal compound examples include the following compounds (1) to (17).
- the polymerizable liquid crystal compound is not limited to the following examples.
- X 1 independently represents an integer of 2 to 5.
- Examples of the polymerizable liquid crystal compound other than those exemplified above include cyclic organopolysiloxane compounds as disclosed in Japanese Patent Application Laid-Open No. 57-165480.
- the ink may contain only one type of polymerizable liquid crystal compound, or may contain two or more types.
- the ink contains two or more kinds of polymerizable liquid crystal compounds different from each other.
- the color reproducibility can be further improved.
- the content of the polymerizable liquid crystal compound is preferably 1% by mass to 70% by mass, more preferably 5% by mass to 60% by mass, and 15% by mass to 45% by mass with respect to the total amount of the ink. It is particularly preferable to have.
- the first ink, the second ink, and the third ink are at least one of the type of the polymerizable liquid crystal compound and the content of the polymerizable liquid crystal compound.
- the pitch of the spiral structure when the polymerizable liquid crystal compound becomes a cholesteric liquid crystal differs, and the wavelength of the light selectively reflected differs.
- ink films having different hues can be obtained. Further, by changing the contents of the polymerizable liquid crystal compounds to each other, the mixing ratio with the chiral compound changes, and ink films having different hues can be obtained.
- Chiral compound Chiral compounds are also referred to as optically active compounds.
- the chiral compound has a function of inducing a helical structure of the polymerizable liquid crystal compound.
- the twisting direction or pitch of the induced spiral structure differs depending on the type and content of the chiral compound.
- the chiral compound is not particularly limited, and is described in a known compound (for example, Liquid Crystal Device Handbook, Chapter 3, Section 4-3, Chiral Agent for TN, STN, p. 199, edited by the 142nd Committee of the Japan Society for the Promotion of Science, 1989. (Description) can be used, and examples thereof include isosorbide derivatives and isomannide derivatives.
- the chiral compound generally contains an asymmetric carbon atom, but may be a compound that does not contain an asymmetric carbon atom as long as it has chirality.
- Examples of the chiral compound include an axial asymmetric compound having a binaphthyl structure, a spiral asymmetric compound having a helicene structure, and a plane asymmetric compound having a cyclophane structure.
- the chiral compound may have a polymerizable group.
- a polymer having a structural unit derived from the polymerizable liquid crystal compound and a structural unit derived from the chiral compound by the polymerization reaction between the chiral compound and the polymerizable liquid crystal compound can be obtained. It is formed.
- the polymerizable group is preferably a group of the same type as the polymerizable group of the polymerizable liquid crystal compound.
- the polymerizable group of the chiral compound is preferably a polymerizable unsaturated group, an epoxy group or an aziridinyl group, more preferably a polymerizable unsaturated group, and particularly preferably an ethylenically unsaturated group. ..
- the chiral compound itself may be a liquid crystal compound.
- chiral compounds include the following compounds.
- the chiral compound that can be used in the ink composition is not limited to the following examples.
- "Me” in the compound means a methyl group.
- X independently represents an integer of 2 to 5.
- the content of the chiral compound is preferably 1 part by mass to 15 parts by mass, and 1.5 parts by mass to 5 parts by mass with respect to 100 parts by mass of the content of the polymerizable liquid crystal compound in the ink composition. Is more preferable.
- the first ink and the second ink have different contents of chiral compounds.
- the third ink it is preferable that the first ink, the second ink, and the third ink have different contents of the chiral compound.
- the pitch of the spiral structure when the polymerizable liquid crystal compound becomes a cholesteric liquid crystal differs, and the wavelength of the light selectively reflected differs.
- ink films having different hues can be obtained.
- the content of the chiral compound is increased, the reflected wavelength tends to shift to the short wavelength side, and when the content of the chiral compound is decreased, the reflected wavelength tends to shift to the long wavelength side.
- Organic solvent is not particularly limited and can be appropriately selected depending on the intended purpose.
- organic solvent examples include a ketone solvent, an alkyl halide solvent, an amide solvent, a sulfoxide solvent, a heterocyclic compound, a hydrocarbon solvent, an ester solvent, and an ether solvent.
- the content of the organic solvent is preferably 20% by mass to 90% by mass, preferably 40% by mass to 80% by mass, and preferably 50% by mass to 80% by mass with respect to the total amount of the ink. More preferred.
- the ink preferably further contains a polymerization initiator.
- the polymerization initiator is preferably a photopolymerization initiator, and more preferably a radical polymerization initiator having a function of generating radicals by irradiation with ultraviolet rays.
- the polymerization initiator examples include an alkylphenone-based photopolymerization initiator, an acylphosphine oxide-based photopolymerization initiator, an intramolecular hydrogen abstraction type photopolymerization initiator, an oxime ester-based photopolymerization initiator, and a cationic photopolymerization initiator. Agents are mentioned. Among them, the polymerization initiator is preferably an acylphosphine oxide-based photopolymerization initiator, and specifically, (2,4,6-trimethylbenzoyl) diphenylphosphine oxide or bis (2,4,6-trimethylbenzoyl) phenyl. Phosphine oxide is preferred.
- the content of the polymerization initiator is preferably 0.1 part by mass to 20 parts by mass, and more preferably 0.5 part by mass to 12 parts by mass with respect to 100 parts by mass of the content of the polymerizable liquid crystal compound. preferable.
- the ink may contain additives as long as the effects of the present disclosure are not impaired.
- the additive examples include a surfactant, a cross-linking agent, and a non-polymerizable polymer for improving the ejection property of the ink.
- the polymerizable liquid crystal compound is horizontally oriented on the air interface side when the ink is cured, and the spiral axis direction is controlled to be more uniform.
- the surfactant a compound capable of functioning as an orientation control agent having a cholesteric structure of planar orientation stably or rapidly is preferable.
- the surfactant include a silicone-based surfactant and a fluorine-based surfactant, and a fluorine-based surfactant is preferable.
- the content of the surfactant is preferably 0.01 part by mass to 10 parts by mass, more preferably 0.01 part by mass to 5 parts by mass, and 0.02 part by mass with respect to 100 parts by mass of the content of the polymerizable liquid crystal compound. Parts to 1 part by mass are more preferable.
- the viscosities of at least two kinds of inks are preferably 7 mPa ⁇ s or more, more preferably 8 mPa ⁇ s or more, and even more preferably 10 mPa ⁇ s or more.
- the upper limit of the viscosity of the ink is, for example, 30 mPa ⁇ s from the viewpoint of ink ejection property.
- the ink droplets landed on the substrate are difficult to spread.
- the boundary of the portion where the image is originally recorded with a different hue becomes unclear, and the fineness of the image tends to decrease.
- the ink droplets do not spread easily, a high-definition image can be obtained.
- the viscosity of the ink is measured at 25 ° C. using a viscometer, for example, using a viscometer (product name "RE-85L", manufactured by Toki Sangyo Co., Ltd.).
- the surface tension of at least two types of ink is preferably 20 mN / m to 40 mN / m, and more preferably 23 mN / m to 35 mN / m.
- the surface tension of the ink is measured at 25 ° C. using a surface tension meter, for example, measured using a surface tension meter (product name "DY-700", manufactured by Kyowa Surface Chemistry Co., Ltd.).
- the maximum value of the absolute value of the difference in surface tension between the inks is preferably 1 mN / m or less, and more preferably 0.7 mN / m or less.
- the inks are mixed in a desired ratio when a mixed region in which at least two kinds of inks are mixed is formed. The area is easy to fix. If the region where the ink is uniformly mixed can be appropriately controlled, the polymerizable liquid crystal compound is uniformly oriented and an image with less color unevenness can be obtained. Further, when the surface tension difference is 1 mN / m or less after the ink is landed on the adjacent region, the occurrence of bleeding can be suppressed.
- the ink preparation step it is preferable to prepare at least two kinds of inks having the same type of polymerizable liquid crystal compound and chiral compound from the viewpoint of ease of mixing the inks with each other. At that time, it is preferable that at least two kinds of inks have different contents of chiral compounds from each other.
- the image recording method of the present disclosure includes a step of heating a base material (hereinafter, also referred to as a “base material heating step”). By preheating the base material, ink can be applied onto the heated base material.
- the base material is not particularly limited, and any base material can be selected.
- the base material may be any of an ink-absorbent base material, an ink-low-absorbent base material, and an ink-non-absorbent base material.
- Examples of the base material include paper, leather, cloth, and resin.
- the base material is preferably an ink non-absorbent base material, and more preferably a resin base material.
- the resin constituting the resin base material examples include cellulose diacetate, cellulose triacetate, cellulose propionate, cellulose butyrate, cellulose acetate butyrate, cellulose nitrate, acrylic resin, chlorinated polyolefin resin, polyether sulfone resin, and polyethylene terephthalate. (PET), polyethylene naphthalate, nylon, polyethylene, polystyrene, polypropylene, polycycloolefin resin, polyimide resin, polycarbonate resin, and polyvinyl acetal.
- the resin base material may be a base material containing only one of these resins, or may be a base material in which two or more types are mixed.
- the thickness of the base material is not particularly limited, and is, for example, 1 ⁇ m to 10 mm.
- the means for heating the base material is not particularly limited, and examples thereof include a heat drum, hot air, an infrared lamp, an oven, a heat plate, and a hot plate.
- the heating temperature of the base material is preferably 40 ° C. or higher, more preferably 50 ° C. to 100 ° C., and even more preferably 55 ° C. to 80 ° C.
- the image recording method of the present disclosure includes a step of applying at least two kinds of inks on a heated substrate by using an inkjet recording method (hereinafter, also referred to as “ink application step”).
- ink application step at least a part of the substrate is applied to form a mixed region in which at least two kinds of inks are mixed.
- various colors can be reproduced with high color development by forming a mixed region in which at least two kinds of inks are mixed by applying the ink to at least a part of the base material. Further, by applying the ink onto the heated base material, the ink droplets landed on the base material are less likely to spread. The ink droplets do not spread easily, and the ink droplets stay at the landing position, so that a high-definition image can be obtained.
- the mixed region in which at least two kinds of inks are mixed may be formed in at least a part of the substrate. That is, a mixed region may be formed on the entire surface of the substrate. Further, as long as the mixed region is formed in a part of the base material, the mixed region may not be formed in the other part of the base material.
- the mixed region means a region in which at least two kinds of inks are mixed on the substrate.
- Specific embodiments in which the mixed region is formed include the following two embodiments.
- At least two types of ink are continuously ejected, at least two types of ink are mixed by landing the ink to be ejected later on the ink landing region formed by the ink ejected earlier. Will be done.
- at least two kinds of inks are ejected at the same time, at least two kinds of inks are mixed by landing so that at least a part of the ink landing areas formed by the at least two kinds of inks overlap each other.
- the "mixed region" of the present disclosure at least two types of ink are ejected so that the ink landing regions do not overlap each other, and then the ink landing regions become one with each other as the ink spreads on the substrate. Areas that overlap are not included.
- the mixed region is formed.
- a fluorescence spectrophotometer product name "FD-7" or the like, it can be confirmed that the reflection wavelength is different from the reflection wavelength of the region other than the mixed region. Further, since the color development property of the mixed region is different from that of the non-mixed region, it can be easily confirmed visually.
- the ink film (also referred to as "ink layer”) formed by applying ink on the base material in the ink applying step is a single layer.
- the image recording method of the present disclosure reduces the number of steps by forming the ink layer so as to be a single layer. be able to.
- the image recording method of the present disclosure since the ink is applied so as to form a single layer, it is possible to obtain an image having high color development as compared with the case where the ink layers are laminated.
- a generally known method can be used, for example, a charge control method for ejecting an ink composition using an electrostatic attraction force, and a drop-on-demand method (pressure pulse method) using the vibration pressure of a piezo element.
- a charge control method for ejecting an ink composition using an electrostatic attraction force and a drop-on-demand method (pressure pulse method) using the vibration pressure of a piezo element.
- a drop-on-demand method pressure pulse method
- an acoustic inkjet method that converts an electric signal into an acoustic beam and irradiates the ink composition to eject the ink composition using radiation pressure
- an acoustic inkjet method that heats the ink composition to form bubbles and applies the generated pressure.
- the thermal inkjet method to be used can be mentioned.
- the image recording method using an inkjet recording device includes a shuttle scan method (also referred to as a "serial head method") in which an image is recorded using a short serial head, and a recording element corresponding to the entire width direction of the recording medium.
- a single-pass method also referred to as a "line head method” in which an image is recorded using a line head in which the images are arranged.
- the shuttle scan method images are recorded while scanning the serial head in the width direction of the recording medium.
- the single-pass method the image can be recorded on the entire surface of the recording medium by scanning the recording medium in the direction orthogonal to the arrangement direction of the recording elements.
- the single pass method does not require a transport system such as a carriage that scans the serial head. Further, in the single pass method, complicated scanning control between the movement of the carriage and the recording medium becomes unnecessary, and only the recording medium moves, so that the recording speed can be increased as compared with the shuttle scan method.
- the ink applying step it is preferable to apply the total amount of at least two kinds of inks per unit area in the mixing region in the range of 3 g / m 2 to 20 g / m 2 , and 3.5 g / m 2 to 20 g / m. It is more preferably given in the range of m 2 , 3.5 g / m 2 to 18 g / m 2 , and even more preferably given in the range of 3.5 g / m 2 to 16 g / m 2 . It is particularly preferable to give it in the range of 2 to 13 g / m 2 .
- the amount of ink applied is larger than that in the region other than the mixed region.
- the ink applying step it is preferable to apply the amount of ink applied per unit area in one image recording in the range of 3 g / m 2 to 20 g / m 2 even in the area other than the mixed area. It is more preferably given in the range of 5 g / m 2 to 20 g / m 2 , 3.5 g / m 2 to 18 g / m 2 , and further given in the range of 3.5 g / m 2 to 16 g / m 2 . It is preferably applied in the range of 3.5 g / m 2 to 13 g / m 2 .
- the region other than the mixed region means a region in which only one type of ink is applied onto the substrate and at least two types of ink are not mixed.
- the ink applying step it is preferable to apply the total amount of the polymerizable liquid crystal compound contained in at least two kinds of inks per unit area in the mixed region in the range of 1 g / m 2 to 8 g / m 2 . It is more preferably given in the range of 1.5 g / m 2 to 8 g / m 2 , and even more preferably given in the range of 1.5 g / m 2 to 7.5 g / m 2 . Most preferably, it is applied in the range of about 7 g / m 2 .
- the polymerizable liquid crystal compound is more uniformly oriented and an image with high color development can be obtained.
- the ink applying step it is preferable to apply the amount of the polymerizable liquid crystal compound contained in the ink per unit area in the range of 1 g / m 2 to 8 g / m 2 even in a region other than the mixed region. It is more preferably given in the range of .5 g / m 2 to 8 g / m 2 , and even more preferably given in the range of 1.5 g / m 2 to 7.5 g / m 2 . Most preferably, it is applied in the range of 7 g / m 2 .
- the total amount of the organic solvent contained in the ink is larger than that in the region other than the mixed region.
- the ink application step it is preferable to apply the amount of the organic solvent contained in the ink per unit area in the range of 1.5 g / m 2 to 12.5 g / m 2 even in a region other than the mixing region. , 2.5 g / m 2 to 12.5 g / m 2 is more preferable, and 2.5 g / m 2 to 10 g / m 2 is more preferable.
- the amount of ink applied is calculated using the following method.
- An image is recorded on a substrate with an area of 1 m 2 at a desired halftone dot ratio (percentage calculation of the ratio of the portion where the image is recorded to the total area).
- the weight of the base material before image recording and the weight of the base material after image recording are measured, and the amount of ink applied is calculated from the weight difference.
- the amount of ink applied can be arbitrarily changed by setting the halftone dot ratio and adjusting the ink ejection amount of the apparatus.
- the amount of the polymerizable liquid crystal compound contained in the ink is calculated from the amount of the ink applied and the content of the polymerizable liquid crystal compound contained in the ink.
- the amount of the organic solvent applied to the ink is calculated from the amount of the ink applied and the content of the organic solvent contained in the ink.
- the total amount of ink applied in the mixed area is calculated as the total amount applied to each ink.
- the ink applying step it is preferable to apply the ink so that the amount of ink ejected from the inkjet head is 1 pL (picolitre) to 30 pL, and more preferably 2 pL to 10 pL.
- the amount of droplets dropped means the volume of ink ejected from one nozzle at one time by the inkjet recording method.
- the ink applying step it is preferable to apply the ink so that the resolution is 100 dpi (dot per inch) ⁇ 100 dpi to 2400 dpi ⁇ 2400 dpi, and it is more preferable to apply the ink so that the resolution is 200 dpi ⁇ 200 dpi to 1200 dpi ⁇ 1200 dpi.
- dpi means the number of dots per 25.4 mm.
- the thickness of the ink film formed by at least two kinds of inks is preferably applied so as to be 1 ⁇ m to 20 ⁇ m in one image recording in the mixed region, and is preferably 1 ⁇ m to 15 ⁇ m. It is more preferable to give it as such.
- the ink film is applied so that the thickness of the ink film is 1 ⁇ m to 20 ⁇ m, the applied ink is easily dried, the polymerizable liquid crystal compound is more uniformly oriented, and an image with high color development can be obtained.
- the image recording method of the present disclosure includes a step of irradiating at least two types of ink with active energy rays (hereinafter, also referred to as “active energy ray irradiation step").
- examples of the active energy ray include ultraviolet rays, visible rays, and electron beams, and among them, ultraviolet rays (hereinafter, also referred to as “UV”) are preferable.
- the exposure amount of ultraviolet rays is preferably 20 mJ / cm 2 to 5 J / cm 2 , and more preferably 100 mJ / cm 2 to 1,500 mJ / cm 2 .
- the irradiation conditions and the basic irradiation method the irradiation conditions and the irradiation method disclosed in Japanese Patent Application Laid-Open No. 60-132767 can be applied.
- the irradiation method is a method in which light sources are provided on both sides of the head unit including an ink ejection device and the head unit and the light source are scanned by a so-called shuttle method, or a method performed by another light source without driving. preferable.
- Mercury lamps, gas lasers and solid-state lasers are mainly used as light sources for ultraviolet irradiation, and mercury lamps, metal halide lamps and ultraviolet fluorescent lamps are widely known.
- UV-LED light emitting diode
- UV-LD laser diode
- the light source for ultraviolet irradiation is preferably a metal halide lamp, a high-pressure mercury lamp, a medium-pressure mercury lamp, a low-pressure mercury lamp, or a UV-LED.
- the inkjet recordings of the present disclosure include a substrate and an ink film containing a liquid crystal polymer provided on the substrate, and the ink film includes a plurality of regions having different maximum reflection wavelengths in a plan view. , The orientation of the liquid crystal polymer changes continuously between two adjacent regions.
- the inkjet recorded material of the present disclosure is preferably an inkjet recorded material obtained by the above image recording method.
- the polymerizable liquid crystal compound is polymerized to form an ink film containing the liquid crystal polymer.
- the ink film contains a plurality of regions having different maximum reflection wavelengths in a plan view, various colors are reproduced with high color development.
- the orientation state of the liquid crystal polymer between two adjacent regions can be confirmed by the following method.
- the ink film is cut in the thickness direction of the ink film so as to include a plurality of regions having different maximum reflection wavelengths from each other, and a sample is obtained.
- a scanning electron microscope model "S-4800", manufactured by Hitachi High-Technologies Corporation, observation magnification: 10000 times, acceleration voltage: 2.0 kV
- one cycle of the dark and light striped areas corresponds to the twist of the liquid crystal display of 180 degrees. Therefore, the two cycles of the dark region, the light region, the dark region, and the light region of the striped pattern correspond to 360 degrees of the twist of the liquid crystal display. That is, the width of two cycles of shading representing the striped pattern corresponds to the length of the spiral pitch in the cholesteric liquid crystal phase.
- the ink film contains a plurality of regions having different maximum reflection wavelengths
- the two adjacent regions also have different maximum reflection wavelengths. Therefore, in the two adjacent regions, the lengths of the spiral pitches in the cholesteric liquid crystal phase are different from each other. At this time, attention is paid to between two adjacent regions, and when the length of the spiral pitch changes continuously, it is determined that the orientation state of the liquid crystal polymer changes continuously.
- the viscosity of the ink is a value measured by keeping the liquid temperature at 25 ° C. and using a viscometer (product name "RE-85L", manufactured by Toki Sangyo Co., Ltd.).
- the surface tension of the ink is a value measured using a surface tension meter (product name "DY-700", manufactured by Kyowa Surface Chemistry Co., Ltd.).
- Ink preparation (Ink Bm1) Ink Bm1 was prepared by mixing the components shown below.
- the viscosity (25 ° C.) of the ink Bm1 was 11 mPa ⁇ s. -Diethylene glycol diethyl ether ... 61.27 parts by mass-Mixture of polymerizable liquid crystal compound A1 ... 35 parts by mass-Polymerization initiator: Bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide (product name "Omnirad 819”) ... 1.5 parts by mass, chiral compound A ...
- the mixture of the polymerizable liquid crystal compound is It is a mixture of the following proportions.
- Mixture of polymerizable liquid crystal compound A2 50% by mass of compound (10), 50% by mass of compound (12)
- Compounds (10) to (12) are rod-shaped liquid crystal compounds.
- the maximum reflection wavelength of the ink Bm1 was 440 nm. It was the ink that forms the ink film of. Moreover, when the polarization characteristics were measured using the left circular polarizing plate, no reflection spectrum was obtained. That is, the ink composition Bm1 was an ink that forms an ink film of right-polarized blue. The surface tension of the ink Bm1 was 28 mN / m. The other inks were also measured by the same method as the ink Bm1 unless otherwise specified.
- Ink Rm1 Except for changing the content of chiral compound A in ink Bm1 from 2.2 parts by mass to 1.6 parts by mass and adjusting the content of diethylene glycol diethyl ether so that the total content of ink is the same as that of ink Bm1.
- the viscosity (25 ° C.) of the ink Rm1 was 11 mPa ⁇ s.
- the ink Rm1 was an ink that forms a right-polarized red ink film that reflects right-handed circularly polarized light having a maximum reflection wavelength of 620 nm.
- the surface tension of the ink Rm1 was 27.6 mN / m.
- a PET sheet (product name “Viewful UV TP-188", manufactured by Kimoto Co., Ltd.) was used as a base material.
- the base material was placed on a hot plate prepared by laminating a rubber heater on a metal plate, and heated so that the temperature of the base material became 60 ° C.
- Ink Bm1 and ink Rm1 were ejected onto a substrate heated to 60 ° C. using an inkjet printer (product name “UJF3042HG”, manufactured by Mimaki Engineering Co., Ltd.).
- the ratios of the applied amounts of ink Bm1 and ink Rm1 are 100: 0, 83:17, 2: 1, 50:50, 1: 2, 17:83, and 0: 100, respectively.
- UV-A ultraviolet A wave
- CSOT-40 manufactured by GS Yuasa
- the metal halide lamp irradiation was performed so that the ultraviolet A wave (UV-A, wavelength 320 to 390 nm) was 350 mJ / cm 2 , and an image record 1 was obtained.
- the image recording object 2 was obtained by the same method as that of the image recording object 1 except that the 7 mm square image was changed to the 2 mm square image.
- Example 2 [Ink preparation] (Ink Gm1) Except for changing the content of chiral compound A in ink Bm1 from 2.2 parts by mass to 1.9 parts by mass and adjusting the content of diethylene glycol diethyl ether so that the total content of ink is the same as that of ink Bm1.
- the viscosity (25 ° C.) of the ink Rm1 was 11 mPa ⁇ s.
- the ink Gm1 was an ink that forms a right-polarized green ink film that reflects right-handed circularly polarized light having a maximum reflection wavelength of 510 nm.
- the surface tension of the ink Gm1 was 28 mN / m.
- a PET sheet (product name “Viewful UV TP-188", manufactured by KIMOTO Co., Ltd.) was used as a base material.
- the base material was placed on a rubber heater and heated so that the temperature of the base material became 60 ° C.
- Ink Bm1, ink Rm1, and ink Gm1 were ejected onto a substrate heated to 60 ° C. using an inkjet printer (product name “UJF3042HG”, manufactured by Mimaki Engineering Co., Ltd.).
- the ratio of the amount of ink Bm1, ink Rm1, and ink Gm1 applied is 1: 0: 0, 2: 1: 0, 1: 2: 0, 0: 1: 0, 0: 2, respectively.
- Image data adjusted to be 1, 0: 1: 2, and 0: 0: 1 were prepared.
- the amount of ink droplets was adjusted so that the total amount of ink applied in each image area was 15 g / m 2 , and the same image as in Example 1 was recorded without gaps.
- the metal halide lamp mounted on the ultraviolet irradiation device (product name "CSOT-40", manufactured by GS Yuasa) is installed after holding the substrate at 60 ° C for 1 minute and heating the substrate at 80 ° C for 5 minutes.
- the ultraviolet A wave (UV-A, wavelength 320 to 390 nm) was irradiated so as to be 350 mJ / cm 2 , and an image recording object 1 and an image recording object 2 were obtained.
- Example 3 In Example 1, the image recording object 1 and the image recording are performed by the same method as in Example 1 except that the amount of ink droplets is adjusted so that the total amount of ink applied in each image area is 7 g / m 2 . I got the thing 2.
- Example 4 Image recordings 1 and image recordings 2 were obtained in the same manner as in Example 3 except that the temperature of the base material when ejecting ink was changed to 50 ° C. in Example 3.
- Example 5 In Example 3, the temperature of the base material when ejecting ink was changed to 80 ° C., and after the image recording was completed, the base material was held at 80 ° C. for 5 minutes by the same method as in Example 3. Image recording material 1 and image recording material 2 were obtained. That is, in Example 5, no additional heating was performed on the base material.
- Example 6 In Example 5, the temperature of the base material when ejecting ink was changed to 90 ° C., and after the image recording was completed, the base material was held at 90 ° C. for 5 minutes by the same method as in Example 3. Image recording material 1 and image recording material 2 were obtained. That is, in Example 6, no additional heating was performed on the base material.
- Example 7 In Example 2, the image recording object 1 and the image recording are performed by the same method as in Example 2 except that the amount of ink droplets is adjusted so that the total amount of ink applied in each image area is 7 g / m 2 . I got the thing 2.
- Example 8 Image recordings 1 and image recordings 2 were obtained in the same manner as in Example 7 except that the temperature of the base material when ejecting ink was changed to 50 ° C. in Example 7.
- Example 9 In Example 7, the temperature of the base material when ejecting ink was changed to 80 ° C., and after the image recording was completed, the base material was held at 80 ° C. for 5 minutes by the same method as in Example 7. Image recording material 1 and image recording material 2 were obtained. That is, in Example 9, no additional heating was performed on the base material.
- Example 10 the image recording object 1 and the image recording are carried out in the same manner as in Example 7 except that the amount of ink droplets is adjusted so that the total amount of ink applied in each image area is 3 g / m 2 . I got the thing 2.
- Example 11 In Example 7, the image recording material 1 and the image recording object 1 and the image recording object 1 and the image recording object 1 and the image recording object 1 and Image recording 2 was obtained.
- Example 12 In Example 1, the image recording object 1 and the image recording are performed by the same method as in Example 1 except that the amount of ink droplets is adjusted so that the total amount of ink applied in each image area is 21 g / m 2 . I got the thing 2.
- Image recordings 1 and image recordings 2 were obtained in the same manner as in Example 1 except that the substrate was kept at room temperature (25 ° C.) without heating in Example 1.
- Example 2 Image recordings 1 and image recordings 2 were obtained in the same manner as in Example 2 except that the substrate was kept at room temperature (25 ° C.) without heating in Example 2.
- Ink preparation (Ink Bm2) Ink Bm2 was prepared by mixing the components shown below.
- the viscosity (25 ° C.) of the ink Bm2 was 6 mPa ⁇ s. -Diethylene glycol diethyl ether ... 68.27 parts by mass-Mixture of polymerizable liquid crystal compound A1 ... 28 parts by mass-Polymerization initiator: Bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide (product name "Omnirad 819, IGM Resins" B.V. Co., Ltd. ”) ... 1.5 parts by mass, chiral compound A ...
- Ink Bm2 was an ink forming a right-polarized blue ink film that reflects right-handed circularly polarized light having a selective reflection wavelength of 430 nm.
- the surface tension of the ink Bm2 was 27 mN / m.
- Ink Rm2 Except for changing the content of chiral compound A in ink Bm2 from 2.2 parts by mass to 1.6 parts by mass and adjusting the content of diethylene glycol diethyl ether so that the total content of ink is the same as that of ink Bm2.
- the viscosity (25 ° C.) of the ink Rm1 was 6 mPa ⁇ s.
- the ink Rm2 was an ink that forms a right-polarized red ink film that reflects right-handed circularly polarized light having a maximum reflection wavelength of 620 nm.
- the surface tension of the ink Rm2 was 27 mN / m.
- Example 14 [Ink preparation] (Ink Rm3) The content of the fluorosurfactant in the ink Rm1 was changed from 0.03 part by mass to 0.2 parts by mass, and the content of diethylene glycol diethyl ether was adjusted so that the total content of the ink was the same as that of the ink Rm1.
- Ink Rm3 was prepared in the same manner as ink Rm1 except for the above.
- the viscosity (25 ° C.) of the ink Rm3 was 11 mPa ⁇ s.
- the ink Rm2 was an ink that forms a right-polarized red ink film that reflects right-handed circularly polarized light having a maximum reflection wavelength of 620 nm.
- the surface tension of the ink Rm3 was 25 mN / m.
- Table 1 shows the types of ink used in Examples and Comparative Examples; the amount of ink, organic solvent, and polymerizable liquid crystal compound applied; the maximum absolute value of the difference in surface tension; and the basis for ejecting ink. The temperature of the material is described.
- the maximum absolute value of the difference in surface tension was the largest of the calculated absolute values obtained by calculating the absolute value of the difference in surface tension between the inks.
- spectral reflection spectra are measured in seven wavelength regions of wavelengths 420 nm to 460 nm, 465 nm to 475 nm, 480 nm to 520 nm, 525 nm to 550 nm, 555 nm to 565 nm, 570 nm to 605 nm, and 610 nm to 730 nm, and each wavelength region is measured. It was confirmed whether or not it had a reflected wavelength peak. Further, it was confirmed whether or not the same color as that of the image recording object 1 can be visually recognized for the image recording object 2.
- the evaluation criteria are as follows. Table 1 shows the evaluation results.
- ⁇ Evaluation criteria> 7 The image recording material 1 has a reflection wavelength peak having a reflectance of 1% or more in all wavelength regions, and the image recording material 2 has the same color as the image recording material 1 in all wavelength regions. Can be visually recognized as being reproduced.
- 6 A region in which the image recording material 1 has a reflection wavelength peak having a reflectance of 1% or more in all wavelength regions, and the image recording material 2 can reproduce the same color as the image recording material 1. Is 4 to 6. 5: In the image recording material 1, there are six wavelength regions having a reflection wavelength peak having a reflectance of 1% or more, and in the image recording material 2, all the wavelength regions have the same color as the image recording material 1. Can be visually recognized as being reproduced.
- the image recording material 1 In the image recording material 1, there are six wavelength regions having a reflection wavelength peak having a reflectance of 1% or more, and in the image recording material 2, the same color as that of the image recording material 1 can be reproduced. Is 4 or 5.
- 3 The image recording material 1 has five wavelength regions having a reflection wavelength peak having a reflectance of 1% or more, and the image recording material 2 has the same color as the image recording material 1 in all wavelength regions. Can be visually recognized as being reproduced.
- 2 In the image recording material 1, there are five wavelength regions having a reflection wavelength peak having a reflectance of 1% or more, and in the image recording material 2, the same color as that of the image recording material 1 can be reproduced. There are four.
- 1 The image recording material 1 has four or less wavelength regions having a reflection wavelength peak having a reflectance of 1% or more, or the image recording material 2 can reproduce the same color as the image recording material 1. There are 3 or less areas.
- the produced image recording material 1 was placed on a black surface of a concealment rate measuring paper (JIS K 5600), and it was visually observed whether or not there was cloudiness or unevenness in the target observation area. ..
- the target observation area was a mixed area in which at least two types of ink were mixed. When there is no cloudiness or unevenness in the image, it can be said that the uniformity of the image is high.
- the evaluation criteria are as follows. 2 or more is a level at which there is no problem in practical use. Table 1 shows the evaluation results. ⁇ Evaluation criteria> 4: There is no cloudiness or unevenness. 3: There is very little cloudiness or unevenness. 2: There is slight white turbidity or unevenness that can be visually confirmed. 1: There is clear cloudiness or unevenness, and there is a practical problem.
- the prepared image recording material was placed on a black surface of a concealment rate measuring paper (JIS K 5600), and it was visually observed whether or not color mixing was observed between adjacent image regions.
- the evaluation criteria are as follows. 2 or more is a level at which there is no problem in practical use. Table 1 shows the evaluation results. ⁇ Evaluation criteria> 5: No color mixing is seen, or little color mixing is seen. 4: Very slight color mixing is seen. 3: There is a slight color mixture, but the color mixture is not noticeable. 2: Color mixing is seen, and the part where the color is mixed is a little conspicuous. 1: The area where the colors are completely mixed is wide and conspicuous.
- a step of preparing at least two kinds of inks including the first ink and the second ink, a step of heating the base material, and a step of heating the base material are performed.
- the step of applying at least two types of ink including a step of applying at least two types of ink using an inkjet recording method and a step of irradiating at least two types of ink with active energy rays. It was found that the color development in a plurality of wavelength ranges was excellent by applying the ink so as to form a mixed region in which at least two kinds of inks were mixed in at least a part of the substrate. That is, it was found that in Examples 1 to 13, various colors can be reproduced with high color development.
- Comparative Example 1 and Comparative Example 2 since the step of heating the substrate is not included and at least two kinds of inks are not applied on the heated substrate, various colors can be reproduced with high color development. There wasn't.
- Example 1 since the total amount of at least two kinds of inks applied per unit area was applied in the range of 3 g / m 2 to 20 g / m 2 in the mixed region, it is more diverse than that of Example 12. It was possible to reproduce various colors with high color development, suppress white turbidity and unevenness of the image, and obtain a more glossy image.
- Example 2 since the mixture was applied so as to form a mixed region in which three kinds of inks were mixed in a part of the base material, more various colors could be reproduced with high color development as compared with Example 1. rice field.
- Example 3 in the mixed region, the total amount of at least two kinds of inks applied per unit area was applied in the range of 3.5 g / m 2 to 13 g / m 2 , so that it is more diverse than in Example 1. It was possible to reproduce various colors with high color development, suppress cloudiness and unevenness of the image, and obtain a higher-definition and glossy image.
- Example 3 since the temperature of the base material when ejecting ink is 55 ° C. or higher, a wider variety of colors can be reproduced with higher color development than in Example 4, and cloudiness and unevenness of the image are suppressed. Moreover, a higher-definition and glossy image was obtained.
- Example 5 since the temperature of the base material when ejecting ink was 80 ° C. or lower, cloudiness and unevenness of the image were further suppressed as compared with Example 6.
- Example 7 since the total amount of at least two types of ink applied per unit area was 13 g / m 2 or less in the mixed region, more diverse colors could be reproduced with higher color development than in Example 2. , White turbidity and unevenness of the image were suppressed, and a higher-definition and glossy image was obtained. In addition, since three types of inks were used, the color development was excellent as compared with Example 3. Further, in Example 10, since the total amount of at least two kinds of inks applied per unit area was applied in the range of 3 g / m 2 to 20 g / m 2 in the mixed region, it is more diverse than that of Example 11. I was able to reproduce a variety of colors with high color development.
- Example 7 since the temperature of the base material when ejecting ink is 55 ° C. or higher, a wider variety of colors can be reproduced with higher color development than in Example 8, and cloudiness and unevenness of the image are suppressed. Moreover, a higher-definition and glossy image was obtained.
- Example 5 since the viscosities of at least two kinds of inks are 7 mPa ⁇ s or more, more various colors can be reproduced with high color development property as compared with Example 13, and the image becomes cloudy and uneven. Was suppressed.
- Example 5 among the absolute values of the difference in surface tension between the inks, the maximum value is 1 mN / m or less, so that a wider variety of colors can be reproduced with higher color development than in Example 14, and the image can be reproduced. White turbidity and unevenness were suppressed, and a higher-definition image was obtained.
- Example 101 to 103> [Image recording] Examples except that the inkjet recording device was changed to an inkjet printer (product name "SUJV-160", manufactured by Mimaki Engineering Co., Ltd.), the heater temperature was set to 70 ° C., and exposure was performed using an exposure machine provided in the inkjet printer. 1. Image recording material 1 and image recording material 2 were obtained in the same manner as in Example 3 and Example 7.
- Example 3 When the same evaluations as in Example 1, Example 3, and Example 7 were performed, various colors could be reproduced with high color development in Examples 101 to 103 as well.
- Example 200 [Ink preparation] (Ink Nm1) The components shown below were mixed to prepare ink Nm1.
- the viscosity (25 ° C.) of the ink Nm1 was 9 mPa ⁇ s. -Diethylene glycol diethyl ether ... 63.43 parts by mass-Mixture of polymerizable liquid crystal compound ... 35 parts by mass-Polymerization initiator: Bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide (product name "Omnirad 819, IGM Resins B" .V.
- Compounds (10) to (12) are rod-shaped liquid crystal compounds.
- ink Nm2 The components shown below were mixed to prepare ink Nm2.
- the viscosity (25 ° C.) of the ink Nm2 was 1.7 mPa ⁇ s. -Diethylene glycol diethyl ether ... 94.7 parts by mass-Polymer initiator: Bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide (product name "Omnirad 819, manufactured by IGM Resins B.V.”) ... 1.5 Parts by mass, chiral compound A ... 4 parts by mass, fluorophosphite (product name "Futagent 208G", manufactured by Neos) ... 0.03 parts by mass
- a PET sheet (product name "Viewful UV TP-188", manufactured by KIMOTO Co., Ltd.) was used as a base material.
- the base material was placed on a rubber heater and heated so that the temperature of the base material became 60 ° C.
- Ink Nm1 and ink Nm2 were ejected onto a substrate heated to 60 ° C. using an inkjet printer (product name "UJF3042HG”, manufactured by Mimaki Engineering Co., Ltd.).
- An ink image was recorded by variously changing the amount of ink Nm2 applied so that a mixed region in which ink Nm1 and ink Nm2 were mixed was formed at an image resolution of 600 dpi ⁇ 720 dpi.
- the base material is held at 60 ° C. for 1 minute, and the base material is further heated at 80 ° C. for 5 minutes, and then mounted on an ultraviolet irradiation device (product name "CSOT-40", manufactured by GS Yuasa).
- an ultraviolet irradiation device product name "CSOT-40", manufactured by GS Yuasa.
- UV A wave UV-A, wavelength 320 to 390 nm
- an image record 1 was obtained.
- the image recording object 2 was obtained by the same method as that of the image recording object 1 except that the 7 mm square image was changed to the 2 mm square image.
- Examples 15 to 28 Image recordings 1 and images in the same manner as in Examples 1 to 14 except that the mixture A1 of the polymerizable liquid crystal compound was changed to the mixture A2 of the polymerizable liquid crystal compound in Examples 1 to 14. Record 2 was obtained. When the same evaluation as in Examples 1 to 14 was performed, the same results were obtained in Examples 15 to 28.
- Example 104-Example 106 When the inks used in Examples 101 to 103 were evaluated in the same manner as in Example 15, Example 17, and Example 21, the same evaluations as in Example 15, Example 17, and Example 21 were performed. In Examples 104 to 106, various colors could be reproduced with high color development.
- Example 29-Example 42 Image recordings 1 and images in the same manner as in Examples 1 to 14 except that the mixture A1 of the polymerizable liquid crystal compound was changed to the mixture A3 of the polymerizable liquid crystal compound in Examples 1 to 14. Record 2 was obtained. When the same evaluation as in Examples 1 to 14 was performed, the same results were obtained in Examples 29 to 42.
- Example 107 to Example 109 When the inks used in Examples 101 to 103 were evaluated in the same manner as in Examples 29, 31 and 35 in the same manner as in Examples 29, 31 and 35. In Examples 107 to 109, various colors could be reproduced with high color development.
Abstract
Description
<1>第1インク及び第2インクを含む少なくとも2種のインクを準備する工程と、基材を加熱する工程と、加熱された基材上に、少なくとも2種のインクをインクジェット記録方式を用いて付与する工程と、少なくとも2種のインクに対して活性エネルギー線を照射する工程と、を含み、少なくとも2種のインクを付与する工程では、基材上の少なくとも一部において、付与により少なくとも2種のインクが混合された混合領域を形成し、第1インクは、第1重合性液晶化合物を含み、第2インクは、第2キラル化合物を含む、画像記録方法。
<2>第1インクは、第1重合性液晶化合物、第1キラル化合物、及び第1有機溶剤を含み、第2インクは、第2重合性液晶化合物、第2キラル化合物、及び第2有機溶剤を含み、第1インクにより形成されるインク膜の極大反射波長と、第2インクにより形成されるインク膜の極大反射波長との差の絶対値は、100nm以上である、<1>に記載の画像記録方法。
<3>第1インクにより形成されるインク膜の極大反射波長は380nm~490nmであり、第2インクにより形成されるインク膜の極大反射波長は600nm~800nmである、<1>又は<2>に記載の画像記録方法。
<4>少なくとも2種のインクを準備する工程では、第3重合性液晶化合物、第3キラル化合物、及び第3有機溶剤を含む第3インクをさらに準備し、第1インクにより形成されるインク膜の極大反射波長、及び、第2インクにより形成されるインク膜の極大反射波長と、第3インクにより形成されるインク膜の極大反射波長との差の絶対値は、40nm以上である、<1>~<3>のいずれか1つに記載の画像記録方法。
<5>第1インクにより形成されるインク膜の極大反射波長は380nm~490nmであり、第2インクにより形成されるインク膜の極大反射波長は600nm~800nmであり、第3インクにより形成されるインク膜の極大反射波長は500nm~590nmである、<4>に記載の画像記録方法。
<6>少なくとも2種のインクを付与する工程では、混合領域において、少なくとも2種のインクの単位面積当たりの合計付与量を3g/m2~20g/m2の範囲として付与する、<1>~<5>のいずれか1つに記載の画像記録方法。
<7>少なくとも2種のインクを付与する工程では、混合領域において、少なくとも2種のインクに含まれる重合性液晶化合物の単位面積当たりの合計付与量を1.5g/m2~8g/m2の範囲として付与する、<2>~<6>のいずれか1つに記載の画像記録方法。
<8>少なくとも2種のインクを付与する工程では、混合領域において、少なくとも2種のインクに含まれる有機溶剤の単位面積当たりの合計付与量を2.5g/m2~12.5g/m2の範囲として付与する、<2>~<7>のいずれか1つに記載の画像記録方法。
<9>少なくとも2種のインクはいずれも、粘度が7mPa・s以上である、<1>~<8>のいずれか1つに記載の画像記録方法。
<10>少なくとも2種のインクは、インク同士の表面張力の差の絶対値のうち、最大値が1mN/m以下である、<1>~<9>のいずれか1つに記載の画像記録方法。
<11>基材を加熱する工程では、基材を40℃以上に加熱する、<1>~<10>のいずれか1つに記載の画像記録方法。
<12>基材と、前記基材上に設けられた、液晶ポリマーを含むインク膜と、を備え、インク膜は、平面視において、極大反射波長が互いに異なる複数の領域を含み、隣接する2つの領域間において、液晶ポリマーの配向状態が連続的に変化している、インクジェット記録物。
本明細書において「~」を用いて示された数値範囲は、「~」の前後に記載される数値をそれぞれ最小値及び最大値として含む範囲を意味する。
本明細書に段階的に記載されている数値範囲において、ある数値範囲で記載された上限値又は下限値は、他の段階的な記載の数値範囲の上限値又は下限値に置き換えてもよい。また、本明細書に記載されている数値範囲において、ある数値範囲で記載された上限値又は下限値は、実施例に示されている値に置き換えてもよい。
本明細書において、組成物中の各成分の量は、組成物中に各成分に該当する物質が複数存在する場合には、特に断らない限り、組成物中に存在する複数の物質の合計量を意味する。
また、本明細書において、2以上の好ましい態様の組み合わせは、より好ましい態様である。
さらに、本明細書において、「工程」という語は、独立した工程だけでなく、他の工程と明確に区別できない場合であっても、その工程の所期の目的が達成されれば、本用語に含まれる。
本明細書において、「(メタ)アクリレート」は、アクリレート又はメタクリレートを意味する。
本開示の画像記録方法は、第1インク及び第2インクを含む少なくとも2種のインクを準備する工程と、基材を加熱する工程と、加熱された基材上に、少なくとも2種のインクをインクジェット記録方式を用いて付与する工程と、少なくとも2種のインクに対して活性エネルギー線を照射する工程と、を含み、少なくとも2種のインクを付与する工程では、基材上の少なくとも一部において、付与により少なくとも2種のインクが混合された混合領域を形成し、第1インクは、第1重合性液晶化合物を含み、第2インクは、第2キラル化合物を含むことにより、多様な色を発色性高く再現することができる。
本開示の画像記録方法は、第1インク及び第2インクを含む少なくとも2種のインクを準備する工程(以下、「インク準備工程」ともいう)を含む。
(1)第1インクが第1重合性液晶化合物を含み、第2インクが第2重合性液晶化合物及び第2キラル化合物を含む態様
(2)第1インクが第1重合性液晶化合物及び第1キラル化合物を含み、第2インクが第2重合性液晶化合物及び第2キラル化合物を含む態様
(3)第1インクが第1重合性液晶化合物、第1キラル化合物及び第1有機溶剤を含み、第2インクが第2重合性液晶化合物及び第2キラル化合物を含む態様
(4)第1インクが第1重合性液晶化合物、第1キラル化合物及び第1有機溶剤を含み、第2インクが第2重合性液晶化合物、第2キラル化合物及び第2有機溶剤を含む態様
(5)第1インクが第1重合性液晶化合物及び第1有機溶剤を含み、第2インクが第2キラル化合物及び第2有機溶剤を含む態様
透明なポリエチレンテレフタレート基材上に、網点率100%の条件でインクを付与し、50℃で5分間乾燥させ、さらに80℃で5分間乾燥させ、インクに含まれる有機溶剤を完全に除去する。次いで、メタルハライドランプ(製品名「CSOT-40、GSユアサ製)で硬化させることによってインク膜を得る。極大反射波長は、このインク膜を蛍光分光濃度計(製品名「FD-7」、コニカミノルタ製社製)で分光反射率を測定することにより算出される。なお、測定時は基材の下に、隠ぺい率測定紙(規格:JIS K 5600(ISO/FDIS 6504-3:1998)、TP技研製)の黒紙を置き、インク膜が最表層になるようにセットして測色する。
本開示において、重合性液晶化合物とは、重合性基を有する液晶化合物のことである。
液晶化合物は、棒状液晶化合物であっても、円盤状液晶化合物であってもよいが、棒状液晶化合物であることが好ましい。
キラル化合物は光学活性化合物ともいう。キラル化合物は、重合性液晶化合物の螺旋構造を誘起する機能を有する。キラル化合物の種類及び含有量によって、誘起する螺旋構造のねじれ方向又はピッチが異なる。
有機溶剤の種類は特に限定されず、目的に応じて適宜選択することができる。
インクは、さらに重合開始剤を含有することが好ましい。重合開始剤は、光重合開始剤であることが好ましく、紫外線の照射によってラジカルを生成する機能を有するラジカル重合開始剤であることがより好ましい。
インクは、必要に応じ、本開示の効果を損なわない範囲で添加剤を含有することができる。
少なくとも2種のインクの粘度はいずれも、7mPa・s以上であることが好ましく、8mPa・s以上であることがより好ましく、10mPa・s以上であることがさらに好ましい。インクの粘度の上限値は、インクの吐出性の観点から、例えば、30mPa・sである。
本開示の画像記録方法は、基材を加熱する工程(以下、「基材加熱工程」ともいう)を含む。基材をあらかじめ加熱しておくことにより、加熱された基材上に、インクを付与することができる。
本開示の画像記録方法は、加熱された基材上に、少なくとも2種のインクをインクジェット記録方式を用いて付与する工程(以下、「インク付与工程」ともいう)を含む。インク付与工程では、基材上の少なくとも一部において、付与により少なくとも2種のインクが混合された混合領域を形成する。
混合領域の反射波長を、蛍光分光濃度計(製品名「FD-7」)等で測色することにより、混合領域ではない領域の反射波長と異なっていることを確認できる。また、混合領域の発色性は、混合領域ではない領域とは発色性が異なるため、目視でも容易に確認することができる。
所望の網点率(全面積に対する画像が記録される部分の割合を百分率で計算したもの)で、基材上に、1m2の面積で画像を記録する。画像記録前の基材の重量と、画像記録後の基材の重量とを測定し、重量差からインクの付与量を算出する。インクの付与量は、網点率の設定、装置のインク吐出量の調整により任意に変更することができる。
本開示のインクジェット記録物は、基材と、基材上に設けられた、液晶ポリマーを含むインク膜と、を備え、インク膜は、平面視において、極大反射波長が互いに異なる複数の領域を含み、隣接する2つの領域間において、液晶ポリマーの配向状態が連続的に変化している。
[インクの調製]
(インクBm1)
下記に示す成分を混合し、インクBm1を調製した。インクBm1の粘度(25℃)は、11mPa・sであった。
・ジエチレングリコールジエチルエーテル …61.27質量部
・重合性液晶化合物の混合物A1 …35質量部
・重合開始剤:ビス(2,4,6-トリメチルベンゾイル)フェニルホスフィンオキシド(製品名「Omnirad 819」) …1.5質量部
・キラル化合物A …2.2質量部
・フッ素系界面活性剤(製品名「フタージェント208G」、ネオス社製) …0.03質量部
なお、重合性液晶化合物の混合物は、以下の割合で混合させたものである。
重合性液晶化合物の混合物A1:化合物(10)50質量%、化合物(11)50質量%
重合性液晶化合物の混合物A2:化合物(10)50質量%、化合物(12)50質量%
重合性液晶化合物の混合物A3:化合物(10)33質量%、化合物(11)34質量%、化合物(12)33質量%
化合物(10)~(12)は棒状液晶化合物である。化合物(10)、化合物(11)、化合物(12)(X1=2)及びキラル化合物Aの構造は以下のとおりである。
インクBm1におけるキラル化合物Aの含有量を2.2質量部から1.6質量部に変更し、インクの合計含有量がインクBm1と同じになるようにジエチレングリコールジエチルエーテルの含有量を調整したこと以外は、インクBm1と同様の方法でインクRm1を調製した。インクRm1の粘度(25℃)は、11mPa・sであった。インクRm1は、極大反射波長が620nmの右円偏光を反射する右偏光赤色のインク膜を形成するインクであった。インクRm1の表面張力は、27.6mN/mであった。
基材としてPETシート(製品名「ビューフルUV TP-188」、きもと社製)を用いた。基材は、ラバーヒーターを金属版に貼り合わせて作成したホットプレートの上に設置され、基材の温度が60℃になるように加熱した。60℃に加熱された基材上に、インクジェットプリンタ(製品名「UJF3042HG」、ミマキエンジニアリング社製)用いて、インクBm1及びインクRm1を吐出した。画像解像度600dpi×720dpiで、インクBm1とインクRm1の付与量の比率がそれぞれ、100:0、83:17、2:1、50:50、1:2、17:83、及び0:100となるよう調整した7mm角の画像が隙間なく縦一列に並んだデータを作製した。これを上下反転させた画像をその隣に配置した。作製した画像データを用いて、各画像領域におけるインクの合計付与量が15g/m2となるようにインク打滴量を調整し、画像を記録した。画像記録終了後、基材を60℃で1分保持し、さらに基材を80℃で5分加熱した後に、紫外線照射装置(製品名「CSOT-40」、GSユアサ社製)に搭載されているメタルハライドランプを用いて、紫外線A波(UV-A、波長320~390nm)が350mJ/cm2となるように照射し、画像記録物1を得た。
また、7mm角の画像を2mm角の画像に変更した以外は、画像記録物1と同様の方法で、画像記録物2を得た。
[インクの調製]
(インクGm1)
インクBm1におけるキラル化合物Aの含有量を2.2質量部から1.9質量部に変更し、インクの合計含有量がインクBm1と同じになるようにジエチレングリコールジエチルエーテルの含有量を調整したこと以外は、インクBm1と同様の方法でインクGm1を調製した。インクRm1の粘度(25℃)は、11mPa・sであった。インクGm1は、極大反射波長が510nmの右円偏光を反射する右偏光緑色のインク膜を形成するインクであった。インクGm1の表面張力は、28mN/mであった。
基材としてPETシート(製品名「ビューフルUV TP-188」、KIMOTO社製)を用いた。基材は、ラバーヒーターの上に設置され、基材の温度が60℃になるように加熱した。60℃に加熱された基材上に、インクジェットプリンタ(製品名「UJF3042HG」、ミマキエンジニアリング社製)を用いて、インクBm1、インクRm1、及びインクGm1を吐出した。画像解像度600dpi×720dpiで、インクBm1とインクRm1とインクGm1の付与量の比率がそれぞれ、1:0:0、2:1:0、1:2:0、0:1:0、0:2:1、0:1:2、及び0:0:1となるよう調整した画像データを作製した。作製した画像データを用いて、各画像領域におけるインクの合計付与量が15g/m2となるようにインク打滴量を調整し、実施例1と同じ画像を隙間なく記録した。画像記録終了後60℃で1分保持し、さらに基材を80℃で5分加熱した後に、紫外線照射装置(製品名「CSOT-40」、GSユアサ社製)に搭載されているメタルハライドランプを用いて、紫外線A波(UV-A、波長320~390nm)が350mJ/cm2となるように照射し、画像記録物1及び画像記録物2を得た。
実施例1において、各画像領域におけるインクの合計付与量が7g/m2となるようにインク打滴量を調整したこと以外は、実施例1と同様の方法で、画像記録物1及び画像記録物2を得た。
実施例3において、インクを吐出する際の基材の温度を50℃に変更したこと以外は、実施例3と同様の方法で、画像記録物1及び画像記録物2を得た。
実施例3において、インクを吐出する際の基材の温度を80℃に変更し、画像記録終了後、基材を80℃で5分保持したこと以外は、実施例3と同様の方法で、画像記録物1及び画像記録物2を得た。すなわち、実施例5では、基材に対して、追加の加熱は行わなかった。
実施例5において、インクを吐出する際の基材の温度を90℃に変更し、画像記録終了後、基材を90℃で5分保持したこと以外は、実施例3と同様の方法で、画像記録物1及び画像記録物2を得た。すなわち、実施例6では、基材に対して、追加の加熱は行わなかった。
実施例2において、各画像領域におけるインクの合計付与量が7g/m2となるようにインク打滴量を調整したこと以外は、実施例2と同様の方法で、画像記録物1及び画像記録物2を得た。
実施例7において、インクを吐出する際の基材の温度を50℃に変更したこと以外は、実施例7と同様の方法で、画像記録物1及び画像記録物2を得た。
実施例7において、インクを吐出する際の基材の温度を80℃に変更し、画像記録終了後、基材を80℃で5分保持したこと以外は、実施例7と同様の方法で、画像記録物1及び画像記録物2を得た。すなわち、実施例9では、基材に対して、追加の加熱は行わなかった。
実施例7において、各画像領域におけるインクの合計付与量が3g/m2となるようにインク打滴量を調整したこと以外は、実施例7と同様の方法で、画像記録物1及び画像記録物2を得た。
実施例7において、各画像領域におけるインクの合計付与量が1.2g/m2となるようにインク打滴量を調整したこと以外は、実施例7と同様の方法で、画像記録物1及び画像記録物2を得た。
実施例1において、各画像領域におけるインクの合計付与量が21g/m2となるようにインク打滴量を調整したこと以外は、実施例1と同様の方法で、画像記録物1及び画像記録物2を得た。
<比較例1>
実施例1において、基材を加熱せず室温(25℃)に保持したこと以外は、実施例1と同様の方法で、画像記録物1及び画像記録物2を得た。
実施例2において、基材を加熱せず室温(25℃)に保持したこと以外は実施例2と同様にして画像記録物1及び画像記録物2を得た。
[インクの調製]
(インクBm2)
下記に示す成分を混合し、インクBm2を調製した。インクBm2の粘度(25℃)は、6mPa・sであった。
・ジエチレングリコールジエチルエーテル …68.27質量部
・重合性液晶化合物の混合物A1 … 28質量部
・重合開始剤:ビス(2,4,6-トリメチルベンゾイル)フェニルホスフィンオキシド
(製品名「Omnirad 819、IGM Resins B.V.社製」) …1.5質量部
・キラル化合物A …2.2質量部
・フッ素系界面活性剤(製品名「フタージェント208G」、ネオス社製) …0.03質量部
インクBm2は、選択反射波長が430nmの右円偏光を反射する右偏光青色のインク膜を形成するインクであった。インクBm2の表面張力は、27mN/mであった。
インクBm2におけるキラル化合物Aの含有量を2.2質量部から1.6質量部に変更し、インクの合計含有量がインクBm2と同じになるようにジエチレングリコールジエチルエーテルの含有量を調整したこと以外は、インクBm2と同様の方法でインクRm2を調製した。インクRm1の粘度(25℃)は、6mPa・sであった。インクRm2は、極大反射波長が620nmの右円偏光を反射する右偏光赤色のインク膜を形成するインクであった。インクRm2の表面張力は、27mN/mであった。
実施例5において、インクBm1の代わりにインクBm2を、インクRm1の代わりにインクRm2を用いたこと以外は、実施例5と同様の方法で、画像記録物を得た。
[インクの調製]
(インクRm3)
インクRm1におけるフッ素系界面活性剤の含有量を0.03質量部から0.2質量部に変更し、インクの合計含有量がインクRm1と同じになるようにジエチレングリコールジエチルエーテルの含有量を調整したこと以外は、インクRm1と同様の方法でインクRm3を調製した。インクRm3の粘度(25℃)は、11mPa・sであった。インクRm2は、極大反射波長が620nmの右円偏光を反射する右偏光赤色のインク膜を形成するインクであった。インクRm3の表面張力は、25mN/mであった。
[画像記録]
実施例5において、インクRm1の代わりにインクRm3を用いたこと以外は、実施例5と同様の方法で、画像記録物を得た。
(1)複数の波長領域での発色性
作製した画像記録物1を、隠ぺい率測定紙(JIS K 5600)の黒い面上に置いて、分光反射測定器(製品名「FD-7」、コニカミノルタ社製)を用いて、複数の波長領域において分光反射スペクトルを測定することにより、複数の色域における発色性を評価した。測定は、反射測定、観察視野2°、観察光源D50、偏光フィルタ無しの条件で行った。具体的には、波長420nm~460nm、465nm~475nm、480nm~520nm、525nm~550nm、555nm~565nm、570nm~605nm、及び610nm~730nmの7つの波長領域で分光反射スペクトルを測定し、各波長領域に反射波長ピークを有するか否かを確認した。また、画像記録物2について、画像記録物1と同じ色が視認できるか否かを確認した。評価基準は以下のとおりである。表1に評価結果を示す。
<評価基準>
7:画像記録物1において、全ての波長領域で、反射率が1%以上である反射波長ピークを有し、かつ、画像記録物2において、全ての波長領域で、画像記録物1と同じ色が再現できていることが視認できる。
6:画像記録物1において、全ての波長領域で、反射率が1%以上である反射波長ピークを有し、かつ、画像記録物2において、画像記録物1と同じ色が再現できている領域が4~6つである。
5:画像記録物1において、反射率が1%以上である反射波長ピークを有する波長領域が6つであり、かつ、画像記録物2において、全ての波長領域で、画像記録物1と同じ色が再現できていることが視認できる。
4:画像記録物1において、反射率が1%以上である反射波長ピークを有する波長領域が6つであり、かつ、画像記録物2において、画像記録物1と同じ色が再現できている領域が4つ又は5つである。
3:画像記録物1において、反射率が1%以上である反射波長ピークを有する波長領域が5つであり、かつ、画像記録物2において、全ての波長領域で、画像記録物1と同じ色が再現できていることが視認できる。
2:画像記録物1において、反射率が1%以上である反射波長ピークを有する波長領域が5つであり、かつ、画像記録物2において、画像記録物1と同じ色が再現できている領域が4つである。
1:画像記録物1において、反射率が1%以上である反射波長ピークを有する波長領域が4つ以下であるか、又は、画像記録物2において、画像記録物1と同じ色が再現できている領域が3つ以下である。
作製した画像記録物1を、隠ぺい率測定紙(規格:JIS K 5600、TP技研製)の黒い面上に置いた。画像を目視で観察し、光沢感を評価した。評価基準は以下のとおりである。2以上は、実用上問題ないレベルである。表1に評価結果を示す。
<評価基準>
4:光沢感に優れる。
3:光沢感がある。
2:光沢感が少しある。
1:光沢感がなく、色が濁って見える。
作製した画像記録物1を、隠ぺい率測定紙(JIS K 5600)の黒い面上に置いて、対象とする観察領域に、白濁又はムラがないか否かを目視で観察した。対象とする観察領域は、少なくとも2種のインクが混合された混合領域とした。画像に、白濁及びムラがない場合には、画像の均一性が高いといえる。評価基準は以下のとおりである。2以上は、実用上問題ないレベルである。表1に評価結果を示す。
<評価基準>
4:白濁及びムラがない。
3:白濁又はムラがごくわずかにある。
2:目視で確認できる白濁又はムラがわずかにある。
1:白濁又はムラが明確にあり、実用上問題がある。
作製した画像記録物を、隠ぺい率測定紙(JIS K 5600)の黒い面上に置いて、隣接する画像領域間で、色の混合が見られるか否かを目視で観察した。評価基準は以下のとおりである。2以上は、実用上問題ないレベルである。表1に評価結果を示す。
<評価基準>
5:色の混合が全く見られないか、又は、色の混合がほとんど見られない。
4:色の混合がごくわずかに見られる。
3:色の混合がわずかに見られるが、色の混合している部分が目立たない。
2:色の混合が見られ、色の混合している部分がやや目立つ。
1:色が完全に混合している領域が広く目立つ。
[画像記録]
インクジェット記録装置を、インクジェットプリンタ(製品名「SUJV-160」、ミマキエンジニアリング社製)に変更し、ヒーター温度を70℃とし、インクジェットプリンタに備え付けの露光機を用いて露光したこと以外は、実施例1、実施例3、及び実施例7と同様の方法で、画像記録物1及び画像記録物2を得た。
[インクの調製]
(インクNm1)
下記に示す成分を混合し、インクNm1を調製した。インクNm1の粘度(25℃)は、9mPa・sであった。
・ジエチレングリコールジエチルエーテル …63.43質量部
・重合性液晶化合物の混合物 …35質量部
・重合開始剤:ビス(2,4,6-トリメチルベンゾイル)フェニルホスフィンオキシド
(製品名「Omnirad 819、IGM Resins B.V.社製」) …1.5質量部
・フッ素系界面活性剤(製品名「フタージェント208G」、ネオス社製) …0.03質量部
なお、重合性液晶化合物の混合物は、化合物(10)33.4質量%、化合物(11)33.3質量%、及び化合物(12)(X1=2)33.3質量%からなる。化合物(10)~(12)は棒状液晶化合物である。
下記に示す成分を混合し、インクNm2を調製した。インクNm2の粘度(25℃)は、1.7mPa・sであった。
・ジエチレングリコールジエチルエーテル …94.7質量部
・重合開始剤:ビス(2,4,6-トリメチルベンゾイル)フェニルホスフィンオキシド
(製品名「Omnirad 819、IGM Resins B.V.社製」) …1.5質量部
・キラル化合物A …4質量部
・フッ素系界面活性剤(製品名「フタージェント208G」、ネオス社製) …0.03質量部
基材としてPETシート(製品名「ビューフルUV TP-188」、KIMOTO社製)を用いた。基材は、ラバーヒーターの上に設置され、基材の温度が60℃になるように加熱した。60℃に加熱された基材上に、インクジェットプリンタ(製品名「UJF3042HG」、ミマキエンジニアリング社製)用いて、インクNm1及びインクNm2を吐出した。画像解像度600dpi×720dpiで、インクNm1及びインクNm2が混合された混合領域が形成されるように、インクNm2の付与量を種々変更して、インク画像を記録した。画像記録終了後、基材を60℃で1分保持し、さらに基材を80℃で5分加熱した後に、紫外線照射装置(製品名「CSOT-40」、GSユアサ社製)に搭載されているメタルハライドランプを用いて、紫外線A波(UV-A、波長320~390nm)を350mJ/cm2となるように照射し、画像記録物1を得た。
また、7mm角の画像を2mm角の画像に変更した以外は、画像記録物1と同様の方法で、画像記録物2を得た。
すなわち、実施例200においても、多様な色を発色性高く再現することができた。
実施例1~実施例14において、重合性液晶化合物の混合物A1を重合性液晶化合物の混合物A2に変更したこと以外は、実施例1~実施例14と同様の方法で、画像記録物1及び画像記録物2を得た。実施例1~実施例14と同様の評価を行ったところ、実施例15~実施例28においても同様の結果が得られた。
実施例101~実施例103において、用いるインクを実施例15、実施例17、及び実施例21と同様にして、実施例15、実施例17、及び実施例21と同様の評価を行ったところ、実施例104~実施例106においても多様な色を発色性高く再現することができた。
実施例1~実施例14において、重合性液晶化合物の混合物A1を重合性液晶化合物の混合物A3に変更したこと以外は、実施例1~実施例14と同様の方法で、画像記録物1及び画像記録物2を得た。実施例1~実施例14と同様の評価を行ったところ、実施例29~実施例42においても同様の結果が得られた。
実施例101~実施例103において、用いるインクを実施例29、実施例31、及び実施例35と同様にして、実施例29、実施例31、及び実施例35と同様の評価を行ったところ、実施例107~実施例109においても多様な色を発色性高く再現することができた。
Claims (12)
- 第1インク及び第2インクを含む少なくとも2種のインクを準備する工程と、
基材を加熱する工程と、
加熱された基材上に、前記少なくとも2種のインクをインクジェット記録方式を用いて付与する工程と、
前記少なくとも2種のインクに対して活性エネルギー線を照射する工程と、を含み、
前記少なくとも2種のインクを付与する工程では、前記基材上の少なくとも一部において、前記付与により前記少なくとも2種のインクが混合された混合領域を形成し、
前記第1インクは、第1重合性液晶化合物を含み、前記第2インクは、第2キラル化合物を含む、画像記録方法。 - 前記第1インクは、前記第1重合性液晶化合物、第1キラル化合物、及び第1有機溶剤を含み、
前記第2インクは、第2重合性液晶化合物、前記第2キラル化合物、及び第2有機溶剤を含み、
前記第1インクにより形成されるインク膜の極大反射波長と、前記第2インクにより形成されるインク膜の極大反射波長との差の絶対値は、100nm以上である、請求項1に記載の画像記録方法。 - 前記第1インクにより形成されるインク膜の極大反射波長は380nm~490nmであり、前記第2インクにより形成されるインク膜の極大反射波長は600nm~800nmである、請求項1又は請求項2に記載の画像記録方法。
- 前記少なくとも2種のインクを準備する工程では、第3重合性液晶化合物、第3キラル化合物、及び第3有機溶剤を含む第3インクをさらに準備し、
前記第1インクにより形成されるインク膜の極大反射波長、及び、前記第2インクにより形成されるインク膜の極大反射波長と、前記第3インクにより形成されるインク膜の極大反射波長と、の差の絶対値は、40nm以上である、請求項1~請求項3のいずれか1項に記載の画像記録方法。 - 前記第1インクにより形成されるインク膜の極大反射波長は380nm~490nmであり、前記第2インクにより形成されるインク膜の極大反射波長は600nm~800nmであり、前記第3インクにより形成されるインク膜の極大反射波長は500nm~590nmである、請求項4に記載の画像記録方法。
- 前記少なくとも2種のインクを付与する工程では、前記混合領域において、前記少なくとも2種のインクの単位面積当たりの合計付与量を3g/m2~20g/m2の範囲として付与する、請求項1~請求項5のいずれか1項に記載の画像記録方法。
- 前記少なくとも2種のインクを付与する工程では、前記混合領域において、前記少なくとも2種のインクに含まれる重合性液晶化合物の単位面積当たりの合計付与量を1.5g/m2~8g/m2の範囲として付与する、請求項2~請求項6のいずれか1項に記載の画像記録方法。
- 前記少なくとも2種のインクを付与する工程では、前記混合領域において、前記少なくとも2種のインクに含まれる有機溶剤の単位面積当たりの合計付与量を2.5g/m2~12.5g/m2の範囲として付与する、請求項2~請求項7のいずれか1項に記載の画像記録方法。
- 前記少なくとも2種のインクはいずれも、粘度が7mPa・s以上である、請求項1~請求項8のいずれか1項に記載の画像記録方法。
- 前記少なくとも2種のインクは、インク同士の表面張力の差の絶対値のうち、最大値が1mN/m以下である、請求項1~請求項9のいずれか1項に記載の画像記録方法。
- 前記基材を加熱する工程では、前記基材を40℃以上に加熱する、請求項1~請求項10のいずれか1項に記載の画像記録方法。
- 基材と、
前記基材上に設けられた、液晶ポリマーを含むインク膜と、を備え、
前記インク膜は、
平面視において、極大反射波長が互いに異なる複数の領域を含み、
隣接する2つの領域間において、液晶ポリマーの配向状態が連続的に変化している、インクジェット記録物。
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Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57165480A (en) | 1981-03-16 | 1982-10-12 | Consortium Elektrochem Ind | Composition having liquid crystal phase and manufacture |
JPS60132767A (ja) | 1983-12-21 | 1985-07-15 | Seikosha Co Ltd | インクジエツトプリンタ |
US4683327A (en) | 1985-06-24 | 1987-07-28 | Celanese Corporation | Anisotropic heat-curable acrylic terminated monomers |
JPH01272551A (ja) | 1988-04-22 | 1989-10-31 | Dainippon Printing Co Ltd | 重合性2官能アクリレートモノマー |
JPH0616616A (ja) | 1992-07-03 | 1994-01-25 | Canon Inc | 反応性液晶性化合物、高分子液晶化合物、液晶組成物および液晶素子 |
JPH07110469A (ja) | 1993-08-16 | 1995-04-25 | Dainippon Ink & Chem Inc | 液晶表示素子及びその製造方法 |
WO1995022586A1 (de) | 1994-02-19 | 1995-08-24 | Basf Aktiengesellschaft | Neue polymerisierbare flüssigkristalline verbindungen |
WO1995024455A1 (de) | 1994-03-11 | 1995-09-14 | Basf Aktiengesellschaft | Neue polymerisierbare flüssigkristalline verbindungen |
WO1997000600A2 (de) | 1995-09-01 | 1997-01-09 | Basf Aktiengesellschaft | Polymerisierbare flüssigkristalline verbindungen |
US5622648A (en) | 1993-10-15 | 1997-04-22 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Reactive liquid crystal compounds |
WO1998023580A1 (de) | 1996-11-27 | 1998-06-04 | Basf Aktiengesellschaft | Polymerisierbare oligomesogene |
US5770107A (en) | 1995-10-05 | 1998-06-23 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Reactive liquid crystalline compound |
WO1998052905A1 (en) | 1997-05-22 | 1998-11-26 | Rolic Ag | New polymerisable liquid crystalline compounds |
JPH1180081A (ja) | 1997-09-05 | 1999-03-23 | Dainippon Ink & Chem Inc | 液晶性(メタ)アクリレート化合物と組成物及びこれを用いた光学異方体 |
JP2001328973A (ja) | 2000-03-13 | 2001-11-27 | Fuji Photo Film Co Ltd | 重合性液晶化合物および光学異方性素子 |
JP2013512800A (ja) * | 2009-12-08 | 2013-04-18 | シクパ ホールディング エスアー | キラル液晶ポリマーマーキング |
JP2014524846A (ja) * | 2011-05-27 | 2014-09-25 | シクパ ホルディング ソシエテ アノニム | 改変された液晶ポリマーマーキングを有する基材 |
WO2018134572A1 (en) * | 2017-01-20 | 2018-07-26 | Johnson Matthey Public Limited Company | Security device, method of making a security device and method of authenticating a product |
WO2020194831A1 (ja) | 2019-03-28 | 2020-10-01 | 富士フイルム株式会社 | インクジェット記録用インクセット及び画像記録方法 |
-
2021
- 2021-12-07 CN CN202180086137.1A patent/CN116601007A/zh active Pending
- 2021-12-07 WO PCT/JP2021/044946 patent/WO2022138142A1/ja active Application Filing
- 2021-12-07 KR KR1020237021719A patent/KR20230109756A/ko active Search and Examination
- 2021-12-07 EP EP21910291.0A patent/EP4269117A1/en active Pending
- 2021-12-07 JP JP2022572091A patent/JPWO2022138142A1/ja active Pending
-
2023
- 2023-06-16 US US18/336,037 patent/US20230339238A1/en active Pending
Patent Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57165480A (en) | 1981-03-16 | 1982-10-12 | Consortium Elektrochem Ind | Composition having liquid crystal phase and manufacture |
JPS60132767A (ja) | 1983-12-21 | 1985-07-15 | Seikosha Co Ltd | インクジエツトプリンタ |
US4683327A (en) | 1985-06-24 | 1987-07-28 | Celanese Corporation | Anisotropic heat-curable acrylic terminated monomers |
JPH01272551A (ja) | 1988-04-22 | 1989-10-31 | Dainippon Printing Co Ltd | 重合性2官能アクリレートモノマー |
JPH0616616A (ja) | 1992-07-03 | 1994-01-25 | Canon Inc | 反応性液晶性化合物、高分子液晶化合物、液晶組成物および液晶素子 |
JPH07110469A (ja) | 1993-08-16 | 1995-04-25 | Dainippon Ink & Chem Inc | 液晶表示素子及びその製造方法 |
US5622648A (en) | 1993-10-15 | 1997-04-22 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Reactive liquid crystal compounds |
WO1995022586A1 (de) | 1994-02-19 | 1995-08-24 | Basf Aktiengesellschaft | Neue polymerisierbare flüssigkristalline verbindungen |
WO1995024455A1 (de) | 1994-03-11 | 1995-09-14 | Basf Aktiengesellschaft | Neue polymerisierbare flüssigkristalline verbindungen |
WO1997000600A2 (de) | 1995-09-01 | 1997-01-09 | Basf Aktiengesellschaft | Polymerisierbare flüssigkristalline verbindungen |
US5770107A (en) | 1995-10-05 | 1998-06-23 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Reactive liquid crystalline compound |
WO1998023580A1 (de) | 1996-11-27 | 1998-06-04 | Basf Aktiengesellschaft | Polymerisierbare oligomesogene |
WO1998052905A1 (en) | 1997-05-22 | 1998-11-26 | Rolic Ag | New polymerisable liquid crystalline compounds |
JPH1180081A (ja) | 1997-09-05 | 1999-03-23 | Dainippon Ink & Chem Inc | 液晶性(メタ)アクリレート化合物と組成物及びこれを用いた光学異方体 |
JP2001328973A (ja) | 2000-03-13 | 2001-11-27 | Fuji Photo Film Co Ltd | 重合性液晶化合物および光学異方性素子 |
JP2013512800A (ja) * | 2009-12-08 | 2013-04-18 | シクパ ホールディング エスアー | キラル液晶ポリマーマーキング |
JP2014524846A (ja) * | 2011-05-27 | 2014-09-25 | シクパ ホルディング ソシエテ アノニム | 改変された液晶ポリマーマーキングを有する基材 |
WO2018134572A1 (en) * | 2017-01-20 | 2018-07-26 | Johnson Matthey Public Limited Company | Security device, method of making a security device and method of authenticating a product |
WO2020194831A1 (ja) | 2019-03-28 | 2020-10-01 | 富士フイルム株式会社 | インクジェット記録用インクセット及び画像記録方法 |
Non-Patent Citations (2)
Title |
---|
ADVANCED MATERIALS, vol. 5, 1993, pages 107 |
MAKROMOL. CHEM, vol. 190, 1989, pages 2255 |
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