WO2023224037A1

WO2023224037A1 - Ultraviolet laser printing paper, printed object, processed article, and printed object production method

Info

Publication number: WO2023224037A1
Application number: PCT/JP2023/018264
Authority: WO
Inventors: 壮佐藤; 祐美石川; 明裕松下; 大信平野
Original assignee: 王子ホールディングス株式会社
Priority date: 2022-05-17
Filing date: 2023-05-16
Publication date: 2023-11-23

Abstract

The present invention provides ultraviolet laser printing paper with which it is possible, when the paper is irradiated with an ultraviolet laser, to obtain printed spots having excellent print clarity at each point. The present invention also provides a printed object obtained by irradiating the ultraviolet laser printing paper with an ultraviolet laser and changing the color of an irradiated region, and a production method for the printed object. Furthermore, the present invention provides a processed article obtained by using the ultraviolet laser printing paper or the printed object.　This ultraviolet laser printing paper has a paper material into which titanium dioxide has been added, the titanium dioxide content in the paper material layer being at least 0.5 mass%, and the titanium dioxide crystallite size being at least 30 nm.

Description

Ultraviolet laser printing paper, printed matter, processed products, and method for producing printed matter

The present invention relates to ultraviolet laser printing paper, printed matter, processed products, and a method for producing printed matter.

Conventionally, labels or inkjet printing have been used to display dates, such as manufacturing dates and shipping dates, and variable information, such as bar codes, on packages such as containers in which contents are housed.
In addition, a method of printing by laser light irradiation has also been proposed. For example, Patent Document 1 describes a method that allows clear printing to be performed at high speed by laser light irradiation, and that the printed portion has excellent resistance to various laser beams. A laminate for laser printing manufactured by applying white ink, black ink, and overprint varnish (OP varnish) on the aluminum-deposited surface of aluminum-deposited paper for the purpose of providing a laminate for printing and its printed body. is disclosed.
Further, Patent Document 2 discloses that the invention includes first titanium oxide particles with an average particle diameter of 150 nm or less, and that generates relatively little heat and is preferably applicable to laser marking of packaging materials. An ink composition used to form a laser marking layer that changes color upon laser irradiation is described.

Japanese Patent Application Publication No. 9-123607 JP2020-75943A

BACKGROUND ART As a means of printing on the surface of a package, a label, an adhesive tape, etc., there is a method of directly applying ink to the surface of the package using a thermal printer or an inkjet printer, which is currently widely used. However, consumables such as ink ribbons for thermal printers and ink for inkjet printers are expensive, and there is a problem in that printing a lot of variable information requires high running costs. Furthermore, if these consumables are not replaced, printing errors may occur. Furthermore, offset printing using UV-curable ink is used to directly print variation information on packages, but dirt on the surface of the package or uneven thickness of the package can cause print fades, missing characters, etc. This may occur.
In addition, although the method described in Patent Document 1 can increase the speed, the upper layer that easily absorbs laser light is removed by irradiation with CO ₂ laser light to expose the lower layer, and the difference in color between the upper and lower layers is eliminated. Since this is a technology for forming characters, etc. that are visible from above, the upper layer is limited to materials that easily absorb laser light, while the lower layer is limited to materials that are difficult to absorb laser light and have a color contrast with the upper layer. be done. In other words, the upper layer is a carbon black material (black) that easily absorbs laser light, the lower layer is a titanium oxide material (white), and the characters formed by laser light irradiation are white on a black background. Poor visibility. Further, when removing the upper layer, there is a problem in that the ink in the upper layer turns into dust, causing contamination of the working environment.
Furthermore, when a coating layer prepared using the ink composition described in Patent Document 2 is printed with an ultraviolet laser, the print clarity of each print spot may be poor.

An object of the present invention is to provide an ultraviolet laser printing paper that, when irradiated with an ultraviolet laser, can provide printing spots with excellent print clarity on a point-by-point basis. Another object of the present invention is to provide a printed matter in which the ultraviolet laser printing paper is irradiated with an ultraviolet laser to change color in the irradiated area, and a method for manufacturing the same. A further object of the present invention is to provide a processed product using the ultraviolet laser printed paper or printed matter.

The present inventors have proposed that in ultraviolet laser printing paper in which titanium oxide is internally added to a paper base material, the content of titanium oxide is set to be a specified amount or more, and the crystallite size of titanium oxide is set to be set to a specified value or more. The inventors have found that the above-mentioned problems can be solved, and have completed the present invention.
The present invention relates to the following <1> to <12>.
<1> An ultraviolet laser printing paper having a paper base material to which titanium oxide is internally added, wherein the content of titanium oxide in the paper base layer is 0.5% by mass or more, and the content of titanium oxide is 0.5% by mass or more. Ultraviolet laser printing paper having a crystallite size of 30 nm or more.
<2> The ultraviolet laser printing paper according to <1>, wherein the titanium oxide has a crystallite size of 53 nm or less.
<3> The ultraviolet laser printing paper according to <1> or <2>, wherein the titanium oxide is rutile titanium oxide, and the titanium oxide has a diffraction angle of 27.60° or less.
<4> The ultraviolet laser printing paper according to any one of <1> to <3>, wherein the length-weighted average fiber length of the pulp constituting the paper base is 0.5 mm or more and 3.0 mm or less.
<5> Any one of <1> to <4>, wherein the number ratio of fine fibers with a fiber length of 0.2 mm or less in the pulp fibers constituting the paper base material is 4% or more and 40% or less. Ultraviolet laser printing paper as described.
<6> The ultraviolet laser printing paper according to any one of <1> to <5>, wherein the content of titanium oxide in the paper base material is 50% by mass or less.
<7> The ultraviolet laser printing paper according to any one of <1> to <6>, which has a sealant layer on at least one surface of the paper base material.
<8> The ultraviolet laser printing paper according to <7>, further comprising a barrier layer.
<9> A printed matter obtained from the ultraviolet laser printing paper according to any one of <1> to <8>, wherein the printed matter contains at least a portion of a printed area containing discolored titanium oxide. and the ratio of the Raman intensity derived from titanium oxide in the printed area to the Raman intensity derived from titanium oxide in the non-printed area is 0.70 or less.
<10> A processed product using the ultraviolet laser printing paper according to any one of <1> to <8> or the printed matter according to <9>.
<11> A method for producing printed matter, comprising the step of printing by irradiating the ultraviolet laser printing paper according to any one of <1> to <8> with an ultraviolet laser to change color in the irradiated area.
<12> The printing step is a step of irradiating an ultraviolet laser such that the ratio of the Raman intensity originating from titanium oxide in the printing area to the Raman intensity originating from titanium oxide in the non-printing area is 0.70 or less. The method for producing a printed matter according to <11>.

According to the present invention, there is provided an ultraviolet laser printing paper that, when irradiated with an ultraviolet laser, provides printing spots with excellent print clarity on a point-by-point basis. Further, according to the present invention, there is provided a printed matter in which the ultraviolet laser printing paper is irradiated with an ultraviolet laser to change color in the irradiated area, and a method for manufacturing the same. Furthermore, according to the present invention, there is provided a processed product using the ultraviolet laser printed paper or printed matter.

[Ultraviolet laser printing paper]
The ultraviolet laser printing paper (hereinafter also simply referred to as "printing paper") of the present invention has a paper base material to which titanium oxide is internally added, and the content of titanium oxide in the paper base material is 0.5. % by mass or more, and the crystallite size of the titanium oxide is 30 nm or more.
According to the present invention, there is provided an ultraviolet laser printing paper that, when irradiated with an ultraviolet laser, provides printing spots with excellent print clarity for each point.
Although the detailed reason for the above-mentioned effects is unknown, some of them are thought to be as follows.
Since titanium oxide is internally added to the paper base material of printing paper, the titanium oxide in the paper base material changes color when irradiated with ultraviolet laser, making it possible to print. The discoloration of the titanium oxide is caused by the ionic valence of the titanium oxide contained in the paper base material changing from 4 to 3 and oxygen defects occurring, causing the color to change from white to black, making it visible. It is thought that it has become. It is thought that the ionic valence of titanium oxide changes when irradiated with light energy corresponding to the band gap of titanium oxide. The band gap of titanium oxide varies depending on the crystal system, but is generally about 3.0 to 3.2 eV, and the corresponding wavelength of light is 420 nm or less. Therefore, even if a laser beam with a wavelength exceeding 420 nm (for example, 532 nm, 1064 nm, 10600 nm) is used, it is difficult to perform printing due to a change in the ion valence of titanium oxide as in the present invention. At this time, by setting the content of titanium oxide in the paper base material to 0.5% by mass or more, printed matter with excellent visibility and excellent printing clarity for each point can be obtained.
In addition, when the crystallite size of titanium oxide is 30 nm or more, there are few crystal defects, the occurrence of recombination of excited electrons and holes is suppressed, and titanium oxide is easily reduced and discolored, so each point can be printed. It is thought that a printed spot with excellent clarity was obtained.
In this embodiment, the printable area refers to the area where the titanium oxide contained in the printing paper changes color, preferably when the titanium oxide in the area irradiated with the ultraviolet laser changes color from white to black due to irradiation with an ultraviolet laser. The printing area refers to the area (portion) where printing is possible, and the printing area refers to the area where the titanium oxide has actually changed color within the printable area, preferably where the titanium oxide has changed color due to irradiation with ultraviolet laser and is visible. It means the part where it is possible, that is, the part that is irradiated with the ultraviolet laser. Furthermore, the non-printable area refers to an area (portion) in which titanium oxide has not changed color, for example, an area (portion) that has not been irradiated with an ultraviolet laser, in the printable area.
The present invention will be explained in more detail below.

Ultraviolet laser printing paper has a paper base material to which titanium oxide is added. The printing paper of this embodiment may be a paper base itself containing titanium oxide, and the printing surface ( A resin layer may be provided on the surface to be printed with an ultraviolet laser.
Moreover, it may have a sealant layer (heat seal layer). By having the sealant layer, the printing paper can have heat-sealing properties.
Furthermore, the paper base material may have a barrier layer mainly for the purpose of blocking the permeation of oxygen gas. The barrier layer is preferably provided on the surface opposite to the printed surface of the paper base material, and when the sealant layer is provided on the surface opposite to the printed surface, the barrier layer is provided between the sealant layer and the paper base material. is preferred.
In addition, the printing paper of this embodiment may have one layer mentioned above, for example, may have a plurality of sealant layers, or may have a plurality of layers. Moreover, it may have a layer other than the layer mentioned above, for example, it may have an adhesive layer, an adhesive layer, etc.

[Paper base material]
The ultraviolet laser printing paper of this embodiment has a paper base material to which titanium oxide is internally added.
The paper base material has titanium oxide added thereto, and the content of titanium oxide in the paper base material is 0.5% by mass or more.
The content of titanium oxide in the paper base material is 0.5% by mass or more, preferably 0.8% by mass or more, more preferably 3.0% by mass or more, even more preferably is 8.0% by mass or more, and from the viewpoint of obtaining a printing spot with excellent printing clarity for each point, from the viewpoint of suppressing the increase in cost due to the printing density reaching a plateau and containing more than the necessary amount of titanium oxide, And from the viewpoint of suppressing the amount of smoke generated during ultraviolet laser irradiation (printing), preferably 50% by mass or less, more preferably 45% by mass or less, still more preferably 35% by mass or less, even more preferably 25% by mass or less, Particularly preferably, it is 15% by mass or less.
If the content of titanium oxide in the paper base material is too high, there is a tendency for smoke to be generated during ultraviolet laser irradiation, which is thought to be due to scattering of titanium oxide. Further, as a result of the generation of smoke, a phenomenon occurs in which discolored titanium oxide is detached from the printing paper, so that the print clarity of each point also tends to deteriorate.
In addition, it is sufficient that the paper base material corresponding to at least the printable area of the printing paper contains titanium oxide, and the area where the content of titanium oxide in the paper base material is less than the above lower limit in the area where printing is not performed. may exist. From the viewpoint of ease of production, it is preferable that the entire area of the paper base material contains titanium oxide at or above the above lower limit.

Each component contained in the paper base material will be explained in detail.
(Titanium oxide)
Titanium oxide contained in the paper base material is represented by the composition formula TiO ₂ and is also called titanium dioxide or titania.
In this embodiment, the crystallite size of titanium oxide in the paper base material is 30 nm or more. When the crystallite size of titanium oxide in the paper base material is less than 30 nm, there are many crystal defects, and the excited electrons and holes excited by ultraviolet laser irradiation are likely to recombine, and as a result, the titanium oxide is reduced. It is difficult to print, and the print clarity of each point is poor. The crystallite size of titanium oxide is preferably 35 nm or more, more preferably 40 nm or more.
Further, the upper limit of the crystallite size of titanium oxide is not particularly limited, but from the viewpoint of dispersion stability in paper stock during paper making, it is preferably 60 nm or less, more preferably 56 nm or less, and even more preferably 53 nm or less. . It is preferable that the upper limit of the crystallite size of titanium oxide is within the above range because the dispersibility of titanium oxide is good even in the obtained paper base material and the printing uniformity is excellent.
The crystallite size of titanium oxide is measured by the method described in Examples.
The crystallite size is determined by the Scherrer equation, and the Bragg angle is the measured value of the maximum strength derived from the 101 plane for anatase titanium oxide and the 110 plane for rutile titanium oxide. use.

Any of the titanium oxides may have a crystalline structure, and is preferably at least one selected from rutile-type titanium oxide, anatase-type titanium oxide, and brookite-type titanium oxide. It is more preferably at least one selected from type titanium oxide and anatase type titanium oxide, and even more preferably rutile type titanium oxide.
The crystal form of titanium oxide can be determined by a known method, and specifically, by Raman spectrum, XRD pattern analysis, etc. For example, when identifying from a Raman spectrum, peaks are generally confirmed at 447±10cm ^-1 and 609±10cm ^-1 for the rutile type, and peaks at 395±10cm ^-1 and 516±10cm for the anatase type. ^-1 , a peak is confirmed at 637±10 cm ^-1 .
One type of titanium oxide may be used alone, or two or more types may be used in combination.

When the titanium oxide is rutile-type titanium oxide, the diffraction angle of the titanium oxide is preferably 27.60° or less from the viewpoint of print clarity for each point. The Bragg angle of rutile-type titanium oxide is originally 27.40°, but if the crystallinity is low, the diffraction angle tends to become high. When the diffraction angle of titanium oxide exceeds 27.60°, crystallinity is low and discoloration is suppressed, so that print clarity for each point tends to be poor.
When the titanium oxide is rutile titanium oxide, the diffraction angle of the titanium oxide is preferably 27.60° or less, more preferably 27.55° or less, and still more preferably 27.50° or less.
In the case of the rutile type, the diffraction angle of titanium oxide is the actual value of the maximum intensity derived from the 110 plane, as described above.

The shape of titanium oxide is not particularly limited, and may be any shape such as amorphous, spherical, rod-like, or needle-like.
When the titanium oxide is amorphous or spherical, the average particle diameter of the titanium oxide is not particularly limited, but from the viewpoint of obtaining printing paper with excellent surface smoothness, it is preferably 0.01 μm or more, more preferably 0.05 μm or more, More preferably 0.10 μm or more, even more preferably more than 0.15 μm, particularly preferably 0.16 μm or more, and preferably 20.0 μm or less, more preferably 5.0 μm or less, even more preferably 1.0 μm. Below, it is still more preferably 0.50 μm or less, particularly preferably 0.30 μm or less.

Further, when the titanium oxide is acicular, the major axis of the titanium oxide is not particularly limited, but from the viewpoint of obtaining printing paper with excellent surface smoothness, it is preferably 0.1 μm or more, more preferably 0.5 μm or more, and It is preferably 1.5 μm or more, and preferably 50.0 μm or less, more preferably 30.0 μm or less, and even more preferably 15.0 μm or less. Further, the short axis is preferably 0.01 μm or more, more preferably 0.03 μm or more, even more preferably 0.05 μm or more, and preferably 3.0 μm or less, more preferably 1.5 μm or less, and even more preferably is 1.0 μm or less. Further, when the titanium oxide is acicular, the aspect ratio (longer axis/breadth axis) is preferably 5 or more, more preferably 10 or more, even more preferably 15 or more, and preferably 300 or less, more preferably It is 100 or less, more preferably 30 or less.
The particle diameter, major axis, and minor axis of titanium oxide are measured by the method described in Examples. Note that the values of the particle diameter, major axis, and minor axis of titanium oxide used as a raw material may be adopted, or the catalog values of the particle diameter, major axis, and minor axis of titanium oxide used as a raw material may be adopted. .

(pulp)
In this embodiment, the printing paper has a paper base material to which titanium oxide is added.
Examples of the raw material pulp constituting the paper base material include wood pulp, non-wood pulp, and deinked pulp. Wood pulp is not particularly limited, but includes, for example, hardwood bleached kraft pulp (LBKP), hardwood unbleached kraft pulp (LUKP), softwood bleached kraft pulp (NBKP), softwood unbleached kraft pulp (NUKP), and sulfite pulp ( Chemical pulp such as SP), dissolving pulp (DP), soda pulp (AP), oxygen bleached kraft pulp (OKP), semi-chemical pulp such as semi-chemical pulp (SCP), chemical ground wood pulp (CGP), ground wood pulp ( Examples include mechanical pulps such as GP), thermomechanical pulp (TMP), and chemithermomechanical pulp (CTMP). Examples of the non-wood pulp include, but are not particularly limited to, cotton-based pulps such as cotton linters and cotton lint, and non-wood-based pulps such as hemp, wheat straw, bamboo, and bagasse. Deinked pulp is not particularly limited, but includes, for example, deinked pulp made from waste paper. The raw material pulp may be used alone or in combination of two or more of the above. Note that the raw material pulp may be mixed with organic synthetic fibers such as polyamide fibers and polyester fibers, recycled fibers such as polynosic fibers, and inorganic fibers such as glass fibers, ceramic fibers, and carbon fibers.
From the viewpoint of easy availability, the raw material pulp is preferably wood pulp or deinked pulp. In addition, among wood pulps, from the viewpoint of uniformity of texture, the raw material pulp is preferably a chemical pulp, more preferably a kraft pulp, and even more preferably a kraft pulp from a hardwood such as eucalyptus or acacia, or a pine or cedar pulp. It is one or more types selected from softwood kraft pulp such as, etc., more preferably one or more types selected from hardwood bleached kraft pulp (LBKP) and softwood bleached kraft pulp (NBKP), and particularly preferably LBKP. .

The length-weighted average fiber length of the pulp constituting the paper base material is preferably 0.5 mm or more, more preferably 0.65 mm or more, and even more preferably 0.7 mm or more, and preferably 3.0 mm or less, more preferably 2.5 mm or less, even more preferably 2.0 mm or less, even more preferably 1.5 mm or less, particularly preferably 1.0 mm or less It is.
If the length-weighted average fiber length of the pulp constituting the paper base material is 3.0 mm or less, the pulps will become tightly entangled with each other, reducing the voids in the paper base material and causing oxidation to occur during ultraviolet laser irradiation. This is preferable because scattering of titanium can be suppressed, smoke generation can be suppressed, and printed matter with excellent clarity from point to point can be obtained. In addition, when the length-weighted average fiber length is 0.5 mm or more, the strength as a paper base material is improved, and the fibers are difficult to fall off from the paper base material when irradiated with an ultraviolet laser, suppressing the generation of paper dust. , is preferable because the amount of smoke generation is suppressed and the printing clarity for each point is excellent.
The length-weighted average fiber length of the pulp constituting the paper base material is measured by the method described in the Examples.

The average fiber width of the pulp constituting the paper base material is preferably 14.0 μm or more, more preferably 15.0 μm or more, even more preferably 15.5 μm or more, even more preferably 16.0 μm or more, and preferably is 35.0 μm or less, more preferably 33.0 μm or less, even more preferably 31.0 μm or less, even more preferably 28.0 μm or less, even more preferably 24.0 μm or less, even more preferably 21.0 μm or less .
When the average fiber width of the pulp constituting the paper base material is 35.0 μm or less, the pulps become tightly intertwined with each other, reducing the voids in the paper base material and causing titanium oxide to scatter during ultraviolet laser irradiation. This is preferable because it can suppress smoke generation, and produce printed matter with excellent printing clarity for each point. In addition, when the average fiber width is 14.0 μm or more, the strength as a paper base material is improved, the fibers are difficult to fall off from the paper sheet medium when irradiated with ultraviolet laser, the generation of paper dust is suppressed, and the amount of smoke generated is This is preferable because it suppresses the problem and provides excellent print clarity for each point.
The average fiber width of the pulp constituting the paper base material can be measured by the method described in Examples.

In the pulp constituting the paper base material, the number ratio of fine fibers with a fiber length of 0.2 mm or less is preferably 4% or more, more preferably 5% or more, still more preferably 6% or more, and even more preferably 10%. Above, it is particularly preferably 15% or more, and preferably 40% or less, more preferably 30% or less, and still more preferably 20% or less.
When the number ratio of fine fibers is 4% or more, the fine fibers are arranged in the sheet to fill the voids between the fibers, so scattering of titanium oxide during ultraviolet laser irradiation is suppressed, and as a result, ultraviolet laser irradiation This is preferable because it suppresses smoke generation and improves the print clarity of each point. Further, it is preferable that the number ratio of fine fibers is 40% or less, because the increase in fine fibers suppresses smoke generation due to scattering of fine fibers during ultraviolet laser irradiation, and improves print clarity for each point.
The number ratio of fine fibers with a fiber length of 0.2 mm or less in the fiber pulp constituting the paper base material is determined by disintegrating the paper base material by the method described in the example, and determining the fiber length of the resulting pulp slurry. It is calculated by measuring with a fiber length measuring device (for example, manufactured by Valmet, model FS-5, equipped with a UHD base unit). Fibers with a fiber length of 0.2 mm or less and a fiber width of 75 μm or less are defined as fine fibers, and the ratio of the number of fine fibers to the number of measured pulps is calculated.

The Canadian standard freeness (CSF) of the wood pulp used for the paper base material is preferably 150 mL or more, more preferably 300 mL or more, and even more preferably 400 mL, from the viewpoint of obtaining the desired fiber width and fiber length. and is preferably 800 mL or less, more preferably 750 mL or less, still more preferably 700 mL or less, even more preferably 600 mL or less.
Here, CSF is Canadian Standard Freeness according to JIS P 8121-2:2012.

The paper base material is obtained by paper-making a pulp slurry to which, in addition to the titanium oxide described above, internal additives are added as necessary.
In addition to the above-mentioned pulp and titanium oxide, the paper base material contains fillers, sizing agents, dry paper strength agents, wet paper strength agents (e.g., polyamide polyamine epichlorohydrin), and retention aids (e.g., sulfuric acid). If necessary, known internal additives for papermaking such as band), drainage improvers, pH adjusters, softeners, antistatic agents, antifoaming agents, dyes and pigments can be added.
Examples of fillers include kaolin, talc, titanium oxide, heavy calcium carbonate, light calcium carbonate, calcium sulfite, gypsum, calcined kaolin, white carbon, amorphous silica, delaminated kaolin, diatomaceous earth, magnesium carbonate, and hydroxide. Examples include aluminum, calcium hydroxide, magnesium hydroxide, and zinc hydroxide.
Examples of the sizing agent include rosin-based, alkyl ketene dimer-based, alkenyl succinic anhydride-based, styrene-acrylic-based, higher fatty acid-based, and petroleum resin-based sizing agents.

When making paper based paper, a known wet paper machine, such as a Fourdrinier paper machine, a gap former paper machine, a cylinder paper machine, a short wire paper machine, etc., may be selected and used as appropriate. Can be done. Next, the paper layer formed by the paper machine is conveyed using felt and dried using a dryer. A multi-stage cylinder dryer may be used as a pre-dryer before drying.

Additionally, the paper base material obtained as described above may be subjected to surface treatment using a calendar to make the thickness and profile uniform, thereby improving printability. For the calendering process, a known calendering machine can be appropriately selected and used.

The paper base material may be single layer or multilayer, and may have a multilayer structure with different pulp compositions.

The basis weight of the paper base material is preferably 30 g/m ² or more, more preferably 40 g/m ² or more, and even more preferably 50 g/m ² or more, from the viewpoint of strength as a printing paper and improving printability. And, preferably it is 1000 g/m ² or less, more preferably 700 g/m ² or less.
The basis weight is measured by the method specified in JIS P 8124:2011.

The thickness of the paper base material is not particularly limited, but from the viewpoint of strength as printing paper and improvement of printability, it is preferably 30 μm or more, more preferably 50 μm or more, even more preferably 70 μm or more, even more preferably 80 μm or more. It is preferably 900 μm or less, more preferably 850 μm or less, and even more preferably 800 μm or less.
The thickness of the paper base material can be measured by the method described in JIS P 8118:2014.

[Resin layer]
The printing paper of this embodiment may further have a resin layer on the paper base material for the purpose of improving the water resistance of the printing paper and for the purpose of functioning as a protective layer. That is, printing paper may be used, in which a resin layer is further provided in advance on a paper base material.

The total light transmittance of the resin layer is preferably 40% or more, more preferably 60% or more, even more preferably 70% or more, even more preferably 80% or more, particularly preferably 90% or more, and 100% or more. % or less. The upper limit is not particularly limited.
Total light transmittance is measured in accordance with JIS K 7361-1:1997.

The resin constituting the resin layer preferably has a total light transmittance of 40% or more, and is not particularly limited as long as it can be provided on a paper base material, but from the viewpoint of transparency and ease of providing the resin layer, When the resin layer and the paper base material are attached via an adhesive layer or laminated together, the material is at least one selected from polyethylene, polypropylene, polyethylene terephthalate, polyvinyl alcohol, and starch. It is preferably at least one selected from polyethylene, polypropylene, polyethylene terephthalate, and polyvinyl alcohol, still more preferably polyethylene and polypropylene, and particularly preferably polyethylene.
When the resin layer is provided by coating, examples include acrylic resin, styrene-maleic acid resin, water-soluble polyurethane resin, and water-soluble polyester resin.
Examples of acrylic resins include resins obtained by copolymerizing (meth)acrylic acid with other monomers such as its alkyl ester, styrene, unsaturated carboxylic acids other than (meth)acrylic acid, ethylene, and propylene. Specific examples include ethylene-(meth)acrylic acid copolymer and styrene-acrylic acid-maleic acid resin, with ethylene-(meth)acrylic acid copolymer being preferred.

The resin layer and paper base material may be laminated by any method, and is not particularly limited, but from the viewpoint of ease of manufacture, the resin layer and paper base material may be laminated via an adhesive layer. , or laminating or applying a transparent paint in the form of a liquid paint.
When providing a resin layer locally, it is preferable to attach it via an adhesive from the viewpoint of ease of manufacture. Furthermore, when providing a resin layer over a wide area, it is preferable to perform lamination processing.
Note that the adhesive layer is not particularly limited, and may be appropriately selected from known adhesive layers. Specifically, the adhesive layer disclosed in JP-A No. 2012-57112 is exemplified.

The thickness of the resin layer is not particularly limited, but from the viewpoint of obtaining clear printing and handling of printed matter and printing paper, it is preferably 5 μm or more, more preferably 10 μm or more, and even more preferably 15 μm or more. , preferably 100 μm or less, more preferably 75 μm or less, even more preferably 50 μm or less.

[Sealant layer]
The printing paper of this embodiment may have a sealant layer on at least one surface of the paper base material. The sealant layer is a layer that is melted and bonded by heating, ultrasonic waves, or the like. The printing paper of this embodiment may have sealant layers on both sides of the paper base material. In addition, from the viewpoint of imparting heat sealability, when a sealant layer is provided, it is preferable to have the sealant layer on the top layer of at least one surface, and even if two or more sealant layers are formed on one surface. good. The sealant layer is preferably provided at least on the surface of the paper base material opposite to the surface on which printing is performed (printing surface), and may also be provided on the surface opposite to the surface on which printing is performed.
Note that the sealant layer may be provided on the entire surface of the paper base material, or may be provided on a portion where heat sealability is required.
By having a sealant layer on at least one surface of the paper base material, heat-sealability is imparted, and a printing paper having heat-sealability is provided. Furthermore, it is preferable that gas barrier properties are also provided by having a sealant layer. Here, gas barrier properties mean barrier properties mainly against at least one selected from oxygen and water vapor, and may also have barrier properties against other gases. It is also preferable that the printing paper of this embodiment has water vapor barrier properties, and in addition, it is also preferable that it has oxygen barrier properties.

The resin constituting the sealant layer (hereinafter also referred to as "sealant layer resin") is not particularly limited, but includes, for example, vinyl chloride resin, vinyl acetate resin, vinyl chloride-vinyl acetate copolymer, acrylic resin, and polyester resin. , olefin resins, styrene resins, styrene acrylic resins (eg, styrene-acrylic acid copolymers), ethylene acrylic resins (ethylene-(meth)acrylic acid copolymers), and modified products thereof. The sealant layer resins may be used alone or in combination of two or more.

As the resin for the sealant layer, either a synthetic product or a commercially available product may be used, and the commercially available products include those used in the examples.

The sealant layer may be formed by laminating by melt extrusion, adhesive, etc., and a method of forming the sealant layer by preparing a coating liquid for the sealant layer and applying the coating liquid is exemplified. As the adhesive, a known adhesive can be used. Note that two or more sealant layers may be formed. Note that when the sealant layer is laminated with a sealant layer resin film using an adhesive or the like, the resin film may be unstretched, or may be uniaxially or biaxially stretched.

When forming a sealant layer by laminating them, the resin for the sealant layer should be selected from the group consisting of polyolefin resins, polyamide resins, polyester resins, and polyvinylidene chloride resins from the viewpoint of heat sealing properties and gas barrier properties. It is more preferable to contain at least one selected kind, it is more preferable to contain a polyolefin resin, and it is even more preferable that it is a polyolefin resin.
In addition, when the sealant layer is a laminated sealant layer consisting of two or more types of layers, from the viewpoint of heat sealability, the surface opposite to the paper base layer is preferably a polyolefin resin layer, and preferably a polyethylene resin layer. More preferred.

From the viewpoint of heat-sealing properties and gas barrier properties, the polyolefin resin is more preferably at least one selected from the group consisting of polyethylene, polypropylene, and ethylene-propylene copolymers, and is at least one of polyethylene and polypropylene. is even more preferable.
Note that the polyethylene may be low density polyethylene (LDPE), linear low density polyethylene (LLDPE), medium density polyethylene (MDPE), or high density polyethylene (HDPE).

Examples of polyamide resins include nylon 6, nylon 11, nylon 12, nylon 66, nylon 610, and nylon 612.

Examples of the polyester resin include polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), and derivatives thereof.
Note that many of the biodegradable resins described below also correspond to polyester resins.

Polyvinylidene chloride resin (PVDC) is a synthetic resin in which vinylidene groups containing chlorine are polymerized, and may be a copolymer with vinyl chloride, acrylonitrile, etc.

Examples of biodegradable resins include polylactic acid (PLA), polybutylene succinate (PBS), polybutylene succinate adipate (PBSA), and 3-hydroxybutanoic acid/3-hydroxyhexanoic acid copolymer (PHBH). Among these, polylactic acid (PLA) and polybutylene succinate (PBS) are preferred, and polybutylene succinate (PBS) is more preferred.

As the sealant layer, a laminated film in which two or more resins are laminated may be used, such as a polyethylene/polypropylene laminated film, a polyamide resin/polyvinylidene chloride resin laminated film, a polyethylene/polyester resin laminated film, etc. be done.

When bonding a sealant layer or a barrier layer (described later) using an adhesive, the adhesive used is not particularly limited and may be solvent-free, organic solvent-based, water-based, etc., but depending on the shape of the paper base material. From the viewpoint of ensuring stability, it is preferable to use an organic solvent type adhesive or a solventless type adhesive.
The main components that make up the adhesive include (meth)acrylic acid ester copolymer, α-olefin copolymer, ethylene-vinyl acetate copolymer, polyvinyl alcohol, polyurethane, styrene-butadiene copolymer, and polyvinyl chloride. , epoxy resin, melamine resin, silicone resin, natural rubber, casein, starch, etc. Among these, preferred are (meth)acrylic acid ester copolymers, ethylene-vinyl acetate copolymers, and polyurethanes, and polyurethanes are more preferred, from the viewpoint of availability and good adhesion.
As the adhesive, commercially available adhesives may be used as appropriate. For example, a combination of Nipporan ID-816 (manufactured by Tosoh Corporation) and HARDENER 300 (manufactured by Tosoh Corporation), Dick Dry LX-500 (manufactured by DIC (manufactured by DIC Corporation) and Dick Dry KW-75 (manufactured by DIC Corporation) is exemplified.
Note that the sealant layer or barrier layer and the paper base material may be laminated after applying the adhesive to the sealant layer or barrier layer, or the paper base material and the sealant layer or barrier layer may be laminated after applying the adhesive to the paper base material. Alternatively, after applying an adhesive to both the sealant layer or barrier layer and the paper base material, both may be laminated. Although not particularly limited, from the viewpoint of shape stability, the sealant layer or barrier layer and the paper base material may be laminated. It is preferable to laminate the paper substrate after applying the adhesive to the layer or barrier layer.

The method for applying the adhesive may be appropriately selected from conventionally known methods, and examples thereof include, but are not limited to, a roll coater, a die coater, a gravure coater, a spray coater, and the like.
The amount of adhesive applied is not particularly limited, but the amount applied after drying (coating amount) is preferably 1 g/m ² or more, from the viewpoint of improving the adhesion between the sealant layer or barrier layer and the paper base layer. It is more preferably 2 g/m ² or more, even more preferably 3 g/m ² or more, and preferably 40 g/m ² or less, more preferably 20 g/m ² or less, even more preferably 10 g/m ² or less.

When forming a sealant layer using a coating liquid, the resin for the sealant layer is not particularly limited as long as it has heat-sealing properties, but examples include styrene-butadiene copolymer; ethylene-acrylic acid copolymer, ethylene-methacrylate. Olefin/unsaturated carboxylic acid copolymers such as acid copolymers; Biodegradable resins; Polyolefin resins such as polyethylene and polypropylene; Methyl acrylate copolymers, methyl methacrylate copolymers, and styrene-acrylic copolymers More preferably, the resin is one or more selected from acrylic resins such as , styrene-methacrylic copolymers, and the like.

Among these, one or more selected from styrene-acrylic acid copolymers and olefin/unsaturated carboxylic acid copolymers are more preferable. In this specification, the acrylic resin does not include an olefin/unsaturated carboxylic acid copolymer.

In olefin/unsaturated carboxylic acid copolymers, the carboxy groups derived from unsaturated carboxylic acid monomers are partially or completely neutralized with alkali metal hydroxides, ammonia, alkylamines, alkanolamines, etc. It may also be salt.
Examples of the olefin monomer of the olefin/unsaturated carboxylic acid copolymer include ethylene, propylene, butadiene, and the like. These may be used alone or in combination of two or more. Among these, ethylene is preferred.

Examples of unsaturated carboxylic acid monomers in the olefin-unsaturated carboxylic acid copolymer include acrylic acid, methacrylic acid, crotonic acid, cinnamic acid, itaconic acid, fumaric acid, maleic acid, and butenetricarboxylic acid. Saturated carboxylic acid; unsaturated polycarboxylic acid alkyl ester having at least one carboxy group, such as itaconic acid monoethyl ester, fumaric acid monobutyl ester, maleic acid monobutyl ester; acrylamide propane sulfonic acid, sulfoethyl sodium acrylate salts, unsaturated sulfonic acid monomers such as sulfopropyl sodium methacrylate, or salts thereof; and the like. These may be used alone or in combination of two or more types. Among these, unsaturated carboxylic acids are preferred, acrylic acid and methacrylic acid are more preferred, and acrylic acid is particularly preferred.
Therefore, the olefin/unsaturated carboxylic acid copolymer is preferably at least one of an ethylene-acrylic acid copolymer and an ethylene-methacrylic acid copolymer.

The ethylene/unsaturated carboxylic acid copolymer is preferably obtained by emulsion polymerization of ethylene and the unsaturated carboxylic acid monomer. As the ethylene-unsaturated carboxylic acid copolymer, ethylene-acrylic acid copolymer and ethylene-methacrylic acid copolymer are preferred. As long as the effects of the present invention are not impaired, the copolymer may be copolymerized with a monomer consisting of ethylene and other compounds copolymerizable with the unsaturated carboxylic acid monomer.

Specific examples of ethylene/unsaturated carboxylic acid copolymers include Zaixen (registered trademark) A, Zaixen (registered trademark) AC (manufactured by Sumitomo Seika Co., Ltd.), and Chemipearl S series (manufactured by Mitsui Chemicals, Inc.). , MFHS1279, MP498345N, MP4983R, MP4990R (manufactured by Michaelman LLC), and the like.

Biodegradable resins include polylactic acid (PLA), polybutylene succinate (PBS), polybutylene succinate adipate (PBSA), polybutylene adipate terephthalate (PBAT), and poly(3-hydroxybutyrate-co-hydroxy Hexanoate) (PHBH), more preferably one or more selected from polylactic acid and polybutylene succinate, particularly preferably polylactic acid. Packaging materials using paper base materials have the advantage of reducing environmental impact compared to packaging materials made of resin films, but by using biodegradable resin as the sealant layer in this embodiment, The environmental load can be further reduced.

As polylactic acid, either a commercially available product or a synthetic product may be used. Examples of commercially available products include Landy PL-1000 and Landy PL-3000 (aqueous dispersion of polylactic acid, manufactured by Miyoshi Oil Co., Ltd.).

When the sealant layer is provided by coating, the coating liquid for the sealant layer contains, in addition to the resin for the sealant layer (water-suspended polymer), a lubricant, a pigment, an antifoaming agent, a viscosity modifier, a surfactant, and a leveling agent. It may contain additives, colorants, etc.
In addition, since these other components tend to deteriorate heat sealability, the total content of other components is preferably 30% by mass or less, more preferably 10% by mass, based on the solid content of the sealant layer. % or less, more preferably 5% by mass or less.

The content of the sealant layer resin in the solid content of the sealant layer coating liquid is preferably 50% by mass or more, more preferably 60% by mass or more, and even more preferably 70% by mass, from the viewpoint of obtaining high heat seal peel strength. That's all.

The device used for coating the coating liquid for the sealant layer is not particularly limited, and may be appropriately selected from commonly used coating devices. For example, air knife coater, blade coater, gravure coater, rod blade coater, roll coater, reverse roll coater, Meyer bar coater, curtain coater, die slot coater, Champlex coater, metering blade type size press coater, short dwell coater, Various known coating devices such as a spray coater, a gate roll coater, and a lip coater can be used.

Drying conditions for the sealant layer are not particularly limited, but the drying temperature is preferably 50 to 120°C, and the drying time is preferably 5 to 120 seconds.
The drying equipment for drying the applied sealant layer is not particularly limited, and any known equipment can be used. Examples of the drying equipment include a hot air dryer, an infrared dryer, an explosion-proof dryer, and a hot plate.

The amount of the sealant layer applied is preferably 1 g/m ² or more, more preferably 2 g/m ^{2 or more, and preferably 30 g/m 2} ^or less, more preferably 20 g/m 2 from the viewpoint of heat seal peel strength. ² or less. In addition, when the printing paper has two or more sealant layers, it is preferable that the total applied amount is within the above range.

[Barrier layer]
The printing paper of this embodiment may further have a barrier layer, and it is preferable to have the barrier layer on the surface opposite to the printing surface of the paper base material. When the printing paper has a sealant layer, it is preferable to have a barrier layer between the paper base material and the sealant layer.
The barrier layer is a layer that mainly has the function of blocking the permeation of oxygen gas. The barrier layer may be formed by applying a coating liquid containing a polymer selected from the group consisting of water-suspended polymers and water-soluble polymers, and by melt-extruding a resin having barrier properties. It may be formed by laminating with an adhesive or the like, or a vapor deposited layer selected from the group consisting of a metal vapor deposited layer and an inorganic vapor deposited layer may be formed, or a vapor deposited layer selected from the group consisting of a metal vapor deposited layer and an inorganic vapor deposited layer. It may also be formed by laminating resin films having vapor deposited layers.

(Water-suspended polymer)
In this embodiment, the water-suspended polymer used in the barrier layer is a polymer whose solubility in water at 25° C. is 10 g/L or less. In this embodiment, the water-suspended polymer is preferably derived from polymers (particles) dispersed in the emulsion.
Water-suspended polymers and water-soluble resins used in the barrier layer are not particularly limited, but include, for example, urethane resins, vinylidene chloride resins, olefin resins, polyester resins, nylon resins, epoxy resins, melamine resins, and polyvinyl resins. Examples include alcohol resins, acrylonitrile resins, polycarboxylic acid resins, and silicone resins. One type of water-suspended polymer may be used alone, or two or more types may be used in combination. Among these, the water-suspended polymer is preferably at least one selected from the group consisting of urethane-based resins and vinylidene chloride-based resins. By forming a barrier layer using these resins, excellent gas barrier properties (oxygen barrier properties) can be exhibited.

Urethane resin can be manufactured by a known manufacturing method. For example, a urethane resin can be obtained by reacting a polyisocyanate compound (for example, a diisocyanate compound) and a polyhydroxy acid (for example, a dihydroxy acid). Further, for example, in addition to the above-mentioned polyisocyanate compound and polyhydroxy acid, it can also be obtained by reaction with a polyol compound (eg, polyester polyol, polyether polyol) and/or a chain extender.
The urethane resin preferably contains at least one selected from the group consisting of structural units derived from metaxylylene diisocyanate and structural units derived from hydrogenated metaxylylene diisocyanate. Such a urethane-based resin exhibits high cohesive force due to hydrogen bonding and the stacking effect of xylylene groups, so that the barrier layer can easily exhibit excellent gas barrier properties. The structural unit derived from metaxylylene diisocyanate refers to a monomer unit reacted with metaxylylene diisocyanate in a urethane resin. The same applies to the structural units derived from hydrogenated metaxylylene diisocyanate and the structural units derived from polyisocyanate. A monomer unit refers to a form in which monomer substances in a polymer are reacted.

In the urethane resin, the total mole% of the constituent units derived from metaxylylene diisocyanate and the constituent units derived from hydrogenated metaxylylene diisocyanate is 50 mole% or more based on the total amount of constituent units derived from the polyisocyanate in the urethane resin. The content is preferably 60 mol% or more, and more preferably 60 mol% or more. The upper limit is not particularly limited, but is preferably 95 mol% or less, more preferably 90 mol% or less. The mole % of the structural units can be identified using known analytical techniques such as ¹ H-NMR.

The urethane resin may have a hydroxyl group, and its hydroxyl value is preferably 50 mgKOH/g or more, more preferably 100 mgKOH/g or more, even more preferably 150 mgKOH/g or more. Note that the upper limit of the hydroxyl value is not particularly limited, but is preferably 1000 mgKOH/g or less, more preferably 800 mgKOH/g or less, and still more preferably 600 mgKOH/g or less. When the hydroxyl value of the urethane resin is within the above range, the barrier layer can easily exhibit oxygen barrier properties. Further, by controlling the hydroxyl value of the urethane resin within the above range, the heat sealability of the barrier layer can be improved, and as a result, the heat sealability of the printing paper can also be improved.
The hydroxyl value is measured according to JIS K0070-1992, and when 1 g of the sample is acetylated, the number of mg of potassium hydroxide required to neutralize the acetic acid bonded to the hydroxyl group is measured.

The urethane resin preferably has an oxygen permeability of 100.0 mL/(m ² ·day · atm) or less, and 50.0 mL/atm at 23 °C and 50% relative humidity when converted to a 25 μm thick sheet. ( ^m2・day・atm) or less, more preferably 25.0mL/( ^m2・day・atm) or less, and 10.0mL/( ^m2・day・atm) or less It is even more preferable that the amount be 3.0 mL/(m ² ·day · atm) or less. Note that the oxygen permeability at 23° C. and 50% relative humidity when converted to a 25 μm thick sheet may be 0 mL/(m ² ·day · atm).
Note that the oxygen permeability when converted to a 25 μm thick sheet is the oxygen permeability measured using a 25 μm thick sheet formed using the target urethane resin. In this specification, the oxygen permeability of the sheet is measured using an oxygen permeability measuring device (OX-TRAN2/22, manufactured by MOCON) under conditions of 23° C. and 50% relative humidity.

The glass transition temperature of the urethane resin is preferably 150°C or lower, more preferably 140°C or lower, and particularly preferably 135°C or lower. Note that the glass transition temperature of the urethane resin is measured in accordance with JIS K 7122:2012.

As the urethane resin, a synthetic product may be used, and examples of the synthetic product include the urethane resin described in International Publication No. 2015/016069. Furthermore, as the urethane resin, commercially available products may be used, such as "Takelac W series (trade name)", "Takelac WPB series (trade name)", "Takelac WS series (trade name)" manufactured by Mitsui Chemicals, Inc. A specific example is Takelac WPB-341. Other commercially available products include "HPU W-003" (hydroxyl value 235 mgKOH/g) manufactured by Dainichiseika Kagyo Co., Ltd.

Vinylidene chloride resin can be manufactured by a known manufacturing method. For example, the vinylidene chloride resin can be obtained from a homopolymer of vinylidene chloride (polyvinylidene chloride, PVDC), a copolymer of vinylidene chloride and a monomer copolymerizable with vinylidene chloride, and the like. Monomers that can be copolymerized with vinylidene chloride include, but are not limited to, vinyl chloride, (meth)acrylic esters such as methyl (meth)acrylate, ethyl (meth)acrylate, and butyl (meth)acrylate. , acrylonitrile, isobutylene, vinyl acetate, etc.

As the vinylidene chloride resin, commercially available products may be used, such as "Saran Latex L549B" manufactured by Asahi Kasei Corporation and Diofan B204 manufactured by Solvay.

The weight average molecular weight of the water-suspended polymer is preferably 1,000 or more and 2,000,000 or less, more preferably 5,000 or more and 5,000,000 or less. In addition, the weight average molecular weight shall employ|adopt the polystyrene equivalent value measured by gel permeation chromatography.

The average particle diameter of the water-suspended polymer in the emulsion is preferably 0.001 μm or more and 100 μm or less, more preferably 0.01 μm or more and 10 μm or less. Note that the average particle diameter can be measured by a dynamic light scattering method.

(Water-soluble polymer)
A water-soluble polymer is a resin that can be dissolved in water. A water-soluble resin is a polymer whose backbone polymer has a solubility in water at 25° C. of more than 10 g/L.
Examples of the polymer serving as the backbone of the water-soluble polymer include polyvinyl alcohol, modified polyvinyl alcohol, starch and its derivatives, cellulose derivatives, polyvinylpyrrolidone, polyacrylic acid and its salts, casein, polyethyleneimine, and the like. Among these, from the viewpoint of improving gas barrier properties, the water-soluble polymer is preferably one or more selected from the group consisting of polyvinyl alcohol and modified polyvinyl alcohol, and more preferably modified polyvinyl alcohol.
Examples of the modified polyvinyl alcohol include ethylene-modified polyvinyl alcohol, carboxy-modified polyvinyl alcohol, silicon-modified polyvinyl alcohol, acetoacetyl-modified polyvinyl alcohol, and diacetone-modified polyvinyl alcohol. Among these, the modified polyvinyl alcohol is preferably one or more selected from the group consisting of ethylene-modified polyvinyl alcohol, carboxy-modified polyvinyl alcohol, silicon-modified polyvinyl alcohol, and acetoacetyl-modified polyvinyl alcohol; and carboxy-modified polyvinyl alcohol, and more preferably ethylene-modified polyvinyl alcohol.
Polyvinyl alcohol and modified polyvinyl alcohol include completely saponified types and partially saponified types, but completely saponified types are preferable. Complete saponification means that the degree of saponification is greater than 96%. Note that the degree of saponification is a value measured by a method based on JIS K 6726:1994.

Commercially available products may be used as the water-soluble polymer; for example, examples of modified polyvinyl alcohol include "Exeval (trade name)" manufactured by Kuraray Co., Ltd.

From the viewpoint of improving barrier properties, the content of the water-suspended polymer and water-soluble polymer in the barrier layer is preferably 10% by mass or more, more preferably 30% by mass or more, based on the solid content of the barrier layer. Preferably it is 50% by mass or more, even more preferably 60% by mass or more, and the upper limit is 100% by mass.

Note that the barrier layer may be formed by applying the barrier layer coating liquid to a paper base material, or by laminating resin films coated with the barrier layer coating liquid in advance. You may. Moreover, the resin film may be a sealant layer.

When forming the barrier layer by coating, it is preferable to contain a layered inorganic compound in addition to at least one selected from the water-suspending polymer and water-soluble polymer described above. That is, it is preferable that the barrier layer contains a water-suspended polymer and a layered inorganic compound, or a water-soluble polymer and a layered inorganic compound. By containing a layered inorganic compound in the barrier layer, the barrier properties can be further improved (oxygen permeability can be further reduced).

The average length of the layered inorganic compound is preferably 1 μm or more and 100 μm or less, more preferably 2 μm or more and 50 μm or less, and even more preferably 3 μm or more and 20 μm or less. Here, the average length of the layered inorganic compound is the average length of the long axis of the layered inorganic compound in the plane direction. When the average length is 1 μm or more, the layered inorganic compound in the barrier layer tends to be arranged parallel to the paper support. Further, when the average length is 100 μm or less, there is less concern that a part of the layered inorganic compound will protrude from the barrier layer.

The aspect ratio of the layered inorganic compound is preferably 200 or more, more preferably 300 or more, still more preferably 500 or more, even more preferably 800 or more. The upper limit of the aspect ratio of the layered inorganic compound is not particularly limited, but is preferably 10,000 or less, more preferably 5,000 or less, and even more preferably 2,000 or less.
When the aspect ratio of the layered inorganic compound is within the above range, the barrier properties are improved, and the coating amount of the barrier layer can be reduced, so that the recyclability and lightness of the printing paper can be improved.
Here, the aspect ratio is a value calculated from an enlarged microscopic photograph of the cross section of the barrier layer, and is the average value of the length of the layered inorganic compound divided by its thickness (the phase ratio of 20 to 30 samples). average value).

The thickness of the layered inorganic compound is preferably 100 nm or less, more preferably 50 nm or less, even more preferably 30 nm or less. Note that the lower limit of the thickness of the layered inorganic compound is not particularly limited, but is preferably 2 nm or more. Here, the thickness of the layered inorganic compound is the average thickness of the layered inorganic compound (arithmetic average value of 20 to 30 samples) measured from an enlarged microscopic photograph of the cross section of the barrier layer. Note that the thickness is defined as the direction perpendicular to the long axis of the layered inorganic compound.
By setting the average thickness of the layered inorganic compound within the above range, the number of layers of the layered inorganic compound in the barrier layer increases, so that the barrier layer can exhibit higher oxygen barrier properties. In particular, when a layered inorganic compound with a large aspect ratio and a small thickness is used, the barrier layer forms a dense film without voids. This phenomenon can also be observed from an enlarged microscopic photograph of the cross section of the barrier layer.

Specific examples of layered inorganic compounds include mica such as mica group and brittle mica group, bentonite, kaolinite (kaolin mineral, hereinafter also referred to as "kaolin"), pyrophyllite, talc, smectite, vermiculite, chlorite, and septechlorite. Examples include stone, serpentine, stilpnomelaine, and montmorillonite. Among these, from the viewpoint of improving water vapor barrier properties, the layered inorganic compound is preferably at least one selected from the group consisting of mica, bentonite, and kaolin, and at least one selected from mica and kaolin. It is preferable to have something. Examples of mica include synthetic mica, muscovite, sericite, phlogopite, biotite, fluorophlogopite (artificial mica), red mica, soda mica, vanadium mica, Examples include illite, chimica, paragonite, and brittle mica. Among these, swellable mica is preferred as mica because it has a high aspect ratio. Further, kaolin may be a natural product or a synthetic product (engineered kaolin).
Among these, at least one selected from the group consisting of mica, bentonite, and kaolin is preferable, and at least one selected from mica and kaolin is more preferable. When the barrier layer contains the above-described layered inorganic compound, the barrier properties of the printing paper under high humidity conditions can be more effectively enhanced.

When the layered inorganic compound is contained in the barrier layer, the content of the layered inorganic compound is not particularly limited, but it is preferably 0.00 parts by mass based on 100 parts by mass of the water-suspended polymer or water-soluble polymer in the barrier layer. 5 parts by mass or more and 500 parts by mass or less, more preferably 1 part by mass or more and 300 parts by mass or less, even more preferably 2 parts by mass or more and 200 parts by mass or less, even more preferably 5 parts by mass or more and 150 parts by mass or less, particularly preferably 10 parts by mass or more It is not less than 70 parts by mass and not more than 70 parts by mass. By controlling the content of the layered inorganic compound within the above range, the barrier properties of the printing paper under high humidity conditions can be more effectively enhanced.

The barrier layer includes at least one selected from a water-suspending polymer and a water-soluble polymer, a layered inorganic compound, and a pigment, a dispersant, a surfactant, an antifoaming agent, a wetting agent, a dye, and a color adjusting agent. , a thickener, etc. may be contained.

When the barrier layer is provided by coating, the coating amount of the coating liquid for the barrier layer is preferably 0.1 g/m ² or more and 10 g/m ² or less, more preferably 0.5 g/m ² or more as solid content. It is 5g/ ^m2 or less.

(Resin with barrier properties)
When the barrier layer is formed by laminating resins having barrier properties by melt extrusion, adhesive, etc., examples of the resins having barrier properties include ethylene-vinyl alcohol copolymer (EVOH) and MX nylon.
As the EVOH, commercially available products may be used, such as the EVAL series manufactured by Kuraray Co., Ltd., for example.
Further, as the MX nylon, MXD6 manufactured by Mitsubishi Gas Chemical Co., Ltd. is exemplified.

(vapor deposited layer)
As a barrier layer, a vapor deposited layer may be formed directly on a paper base material, or a resin film having a vapor deposited layer formed thereon may be laminated to form a barrier layer.
Note that the deposited layer is selected from the group consisting of a metal deposited layer and an inorganic deposited layer.
Aluminum (Al) is exemplified as the vapor-deposited metal of the metal vapor-deposited layer. Furthermore, examples of the inorganic compound to be deposited in the inorganic vapor deposition layer include silica (SiOx) and alumina (AlOx).
The thickness of the metal vapor deposition layer is not particularly limited as long as the desired barrier properties can be obtained.

As a barrier layer, an adhesive may be applied to a resin film provided with a vapor deposition layer, and the resin film may be laminated with a paper base material.
Examples of resin films include polyester resin films such as polyethylene terephthalate (PET), polyamide resin films such as various nylons, polyethylene resins, polypropylene resins, cyclic polyolefin resins, polystyrene resins, and acrylonitrile-styrene copolymers (AS). (resin), acrylonitrile-butadiene-styrene copolymer (ABS resin), polyolefin film such as polybutene resin film, polyvinyl chloride resin, polycarbonate resin, polyimide resin, polyamideimide resin, polyaryl phthalate resin, silicone resins, polysulfone resins, polyphenylene sulfide resins, polyether sulfone resins, polyurethane resins, cellulose resins, poly(meth)acrylic resins, polyvinylidene chloride films, acetal resin films, fluorine resins, etc. Among them, polypropylene resins, polyester resins, and polyamide resins are particularly preferred.

[Printed matter and method of manufacturing printed matter]
The printed matter of this embodiment is a printed matter obtained from the above-mentioned ultraviolet laser printing paper, and has at least a portion of the printed area containing discolored titanium oxide. The ratio of the Raman intensity originating from titanium oxide in the printing area to the Raman intensity originating from titanium oxide in the non-printing area is preferably 0.70 or less. Further, the printed area having the discolored titanium oxide is an area containing titanium oxide that has been discolored by irradiation with an ultraviolet laser, and is an ultraviolet laser irradiation area, that is, a printing area.
Furthermore, the method for manufacturing printed matter of this embodiment includes a step of printing by irradiating the above-described printing paper with an ultraviolet laser to change color in the irradiated area.
As the printing paper used in the method for manufacturing printed matter of this embodiment, the above-mentioned printing paper is exemplified, and the preferable range is also the same. Further, in the method for producing printed matter of the present embodiment, if the content of titanium oxide in the paper base material in at least the ultraviolet laser irradiation area is 0.5% by mass or more, and the crystallite size of titanium oxide is 30 nm or more, Often, the paper substrate in the non-irradiated areas does not have to meet the above requirements.

The ultraviolet laser irradiation is preferably performed such that the ratio of the Raman intensity derived from titanium oxide in the printed area to the Raman intensity derived from titanium oxide in the non-printed area is 0.70 or less. That is, in the printed matter of this embodiment, the ratio of the Raman intensity originating from titanium oxide in the printing area to the Raman intensity originating from titanium oxide in the non-printing area is preferably 0.70 or less.
In the printed matter, the printed area refers to an area (portion) containing discolored titanium oxide in the printable area, and is an area (portion) printed with an ultraviolet laser. The non-printing area means an area (portion) that is not printed in the printable area. In addition, the printable area refers to the area containing titanium oxide, which is the area that can be printed by ultraviolet laser and the area (portion) printed by ultraviolet laser, if any, on ultraviolet laser printing paper or printed matter. The non-printable area means the area other than the printable area on the ultraviolet laser printing paper or printed matter.
The ratio of the Raman intensity originating from titanium oxide in the printing area to the Raman intensity originating from titanium oxide in the non-printing area (Raman intensity in the printing area/Raman intensity in the non-printing area) is 0.70 or less. Printing is preferred. By setting the Raman intensity ratio within the above range, printed matter with excellent visibility can be obtained.
When rutile-type titanium oxide is used as the titanium oxide, the above Raman intensity ratio (Raman intensity of printed area/Raman intensity of non-printed area) is 447 ± 10 cm ^- as the Raman intensity derived from titanium oxide. The Raman intensity of the maximum value in the wave number range of ¹ is compared. Further, when anatase titanium oxide is used as the titanium oxide, the Raman intensity of the maximum value in the wave number range of 516±10 cm ⁻¹ is compared as the Raman intensity derived from titanium oxide.
Note that when rutile-type titanium oxide and anatase-type titanium oxide coexist, the Raman intensity derived from rutile-type titanium oxide is used for comparison.

In the printed matter obtained in this embodiment, it is preferable that the non-printing area is white and the printing area is black.
It is preferable that the non-printing area has a brightness of No. 10 in the Munsell color system, that is, white. On the other hand, the printing area is preferably one of numbers 0 to 8 in the Munsell color system, more preferably numbers 0 to 6, and even more preferably numbers 0 to 4.
In order to obtain the colors in the above Munsell color system, the type and content of titanium oxide in the paper base material of printing paper, the length-weighted average fiber length of the pulp that makes up the paper base material, and other characteristics (paper base It is preferable to adjust the water retention degree of the pulp constituting the material, the amount of fine fibers, the fiber width, etc.) and the irradiation conditions of the ultraviolet laser (for example, average output, repetition frequency, wavelength, etc.) as appropriate.

[Ultraviolet laser irradiation conditions]
The wavelength of the ultraviolet laser is preferably 370 nm or less, more preferably 365 nm or less, even more preferably 360 nm or less, and preferably 260 nm or more, more preferably 340 nm or more, from the viewpoint of improving the visibility of the printed area. More preferably, it is 350 nm or more.

The average output of the ultraviolet laser is preferably 0.3 W or more, more preferably 0.8 W or more, still more preferably 1.2 W or more, even more preferably 1.8 W or more, from the viewpoint of improving the visibility of the printed area. And from the viewpoint of economy, it is preferably 30 W or less, more preferably 25 W or less, even more preferably 20 W or less, even more preferably 15 W or less, even more preferably 10 W or less, even more preferably 6 W or less.

The repetition frequency (frequency) of the ultraviolet laser is preferably 10 kHz or more, more preferably 20 kHz or more, even more preferably 30 kHz or more, and preferably 100 kHz or less, more preferably is 80 kHz or less, more preferably 60 kHz or less.

The spot diameter of the ultraviolet laser is preferably 10 μm or more, more preferably 20 μm or more, even more preferably 30 μm or more, and preferably 300 μm or less, more preferably It is 240 μm or less, more preferably 180 μm or less, even more preferably 120 μm or less.

The scanning speed of the ultraviolet laser is preferably 500 mm/sec or more, more preferably 1000 mm/sec or more, even more preferably 2000 mm/sec or more, and preferably 7000 mm/sec or more, from the viewpoint of high-speed printing and visibility of the printed area. sec or less, more preferably 6000 mm/sec or less, still more preferably 5000 mm/sec or less.

The filling interval (line pitch) of the ultraviolet laser is preferably 10 μm or more, more preferably 20 μm or more, and still more preferably 30 μm or more, from the viewpoint of obtaining a clear image and the ease of obtaining the device. is 300 μm or less, more preferably 250 μm or less, even more preferably 200 μm or less.

[Aspects of printed matter manufacturing method]
The method for producing printed matter of the present invention can be carried out in various ways.
Below, various aspects to which the printed matter manufacturing method of this embodiment can be applied will be illustrated, but the printed matter manufacturing method of this embodiment is not limited to the following aspects. The information to be printed is not particularly limited, but preferably variable information.
It is preferable that the printed matter manufacturing method of this embodiment is performed in-line.
(1) Direct printing on packaging The first embodiment of the method for producing printed matter of this embodiment is a method of printing information on packaging having the printing paper of this embodiment, in which the printed matter is moved on a packaging line. It has a process of directly printing with an ultraviolet laser on the package that is in the middle or intermittently stopped.
In the first method for producing printed matter, a package is produced using the ultraviolet laser printing paper of this embodiment, and directly printed with an ultraviolet laser. Note that it is sufficient that at least the outermost layer of the printed area of the package is made of the above-mentioned printing paper.
Furthermore, examples of the package include cardboard, boxes, etc., and it is preferable to print directly on the side or top surface of the package using an ultraviolet laser.

(2) Printing on Labels The second embodiment of the method for producing printed matter of this embodiment is a method of printing information on a label having the printing paper of this embodiment. The printing paper forming the printing surface of the label is the printing paper of this embodiment.
Preferably, the printed label is applied to the package using a label application device. Various label pasting devices have been proposed as label pasting devices.
The first label pasting device applies an adhesive to a roll of label base paper and then pastes it onto an article. More specifically, there is a cutting means for cutting a roll of label paper into a predetermined length one by one, and a label paper holder coated with adhesive to cut the label paper cut by the cutting means using a label paper holder coated with adhesive. It is equipped with a gluing conveyance means for receiving and applying an adhesive to the back side of the label base paper, and an adhesion means for receiving the label base paper (label) to which adhesive has been applied from the gluing conveyance means and pasting it on an article such as a container. An example of a roll labeler is a roll labeler in which a rotary conveying means having a label holding surface on the outer surface is provided between the cutting means and the gluing conveying means, as disclosed in Japanese Patent Application Laid-Open No. 6-64637.
It also includes a cutting means that cuts the rolled label paper into a predetermined length one by one, a delivery roll that transfers the label paper to the pasting roll, and a gluing roll that applies glue to the label base paper held by the pasting roll. Examples include a roll labeler that has a roll labeler and an embodiment that does not require the delivery roll.
It is preferable that the irradiation with the ultraviolet laser be performed before cutting the rolled label base paper into a predetermined length, or after cutting the label base paper and before transferring it to the next roll or the like. Depending on the configuration of the roll labeler, the front or back side of the label base paper wound into a roll becomes the front or back side when it is attached to the package, so the ultraviolet laser is irradiated accordingly.

The second labeling device uses adhesive label rolls as labels.
When using an adhesive label roll with a release paper, for example, a release paper separating means for separating the adhesive label and the release paper, a delivery roll for receiving the adhesive label from which the release paper has been separated, and a delivery roll for removing the adhesive label from the delivery roll are used. An example is a pasting device that includes a pasting roll that applies suction to a product (packaging body). Irradiation with an ultraviolet laser is preferably carried out before the release paper is separated, or after the release paper is separated and before the film is supported on a pasting roll.
It also has a mechanism that sets an adhesive label roll with release paper, separates the adhesive label and release paper, and affixes the label immediately after separation, and separates the release paper from the set adhesive label roll. An example is an apparatus that prints with an ultraviolet laser during the process. The adhesive label application method described above is also referred to as flow-adhesion.
Furthermore, it has a mechanism for setting an adhesive label roll with release paper and separating the release paper from the adhesive label, and a mechanism for pasting the adhesive label on the article (packaging body), and the pasting mechanism is a syringe type. Examples include a labeling device that uses a , an air jet method, or a robot arm method. It is preferable that the irradiation with the ultraviolet laser be performed from the set pressure-sensitive adhesive label roll with release paper until the release paper is separated.

A linerless adhesive label may be used as the label. Linerless adhesive labels are labels without release paper, and compared to the case of using adhesive label rolls with release paper, the number of labels per roll is larger, and because there is no release paper, they are cheaper. have
A label pasting device using linerless adhesive labels includes a mechanism for setting a linerless label roll, a cutting mechanism for cutting linerless labels one by one, and a mechanism for attaching cut linerless labels to articles (packaging bodies). An example is an apparatus that has a pasting mechanism for pasting, and the pasting mechanism is a cylinder type or a robot arm type. Printing by ultraviolet laser irradiation is preferably carried out between the mechanism that sets the linerless label roll and the cutting mechanism, or while the cut linerless label is sent to the pasting mechanism.

The third label pasting device prints with an ultraviolet laser after pasting the printing paper of this embodiment onto an article (package).
As for the method of attaching a label, the first device and the second device described above are referred to.

(3) Printing on Adhesive Tape The third embodiment of the method for manufacturing printed matter of this embodiment is an embodiment in which adhesive tape is used as printing paper.
That is, the method for producing a printed matter according to the third embodiment includes the step of attaching an adhesive tape made from the printing paper to an article (packaging body), and before or after the attaching step. , has a printing process using an ultraviolet laser.
Alternatively, a printing device in which a printing device using an ultraviolet laser is incorporated into a cardboard sealing machine may be used. Specifically, it has a mechanism for setting the adhesive tape winder, a conveyor for conveying the cardboard, a mechanism for folding the flaps of the cardboard, and a mechanism for applying the adhesive tape to seal the cardboard. It has a mechanism that prints on the adhesive tape with an ultraviolet laser during or after pasting.

The method for producing printed matter according to the present embodiment is not limited to the above embodiments, and can be applied to various uses that require printing.

In this embodiment, the printed material obtained by the method for producing printed material is suitably used for packaging, labels, adhesive tapes, and the like.
Examples of packaging bodies include outer boxes, milk cartons, liquid containers for beverages such as paper cups (preferably liquid paper containers for beverages), and skin packs, and examples of labels include label base paper, adhesive labels, and adhesive sheets. Examples of the adhesive tape include adhesive tape and craft tape.

[Processed goods]
The ultraviolet laser printing paper and printed matter of this embodiment are applied to various processed products. That is, the processed product of this embodiment is made using the ultraviolet laser printing paper of this embodiment or the printed matter of this embodiment.
The processed product of this embodiment is preferably a package, a label, an adhesive tape, or the like.
Examples of packaging include corrugated liner base paper (particularly the outermost liner base paper), outer boxes, milk cartons, liquid containers for beverages such as paper cups (preferably liquid paper containers for beverages), food trays, skin packs, pillows, etc. Examples include packaging, standing pouches, three-sided/four-sided sealed packaging, etc. Examples of labels include label base paper, adhesive labels, and adhesive sheets, and examples of adhesive tapes include adhesive tapes and craft tapes.
A liquid container as an example of a package has, for example, a printed area on its surface. The printing area is irradiated with an ultraviolet laser and characters such as the date are printed on it.

The features of the present invention will be explained in more detail below with reference to Examples and Comparative Examples. The materials, usage amounts, proportions, processing details, processing procedures, etc. shown in the following examples can be changed as appropriate without departing from the spirit of the present invention. Therefore, the scope of the present invention should not be interpreted as being limited by the specific examples shown below.

[Titanium oxide]
Titanium oxide used in Examples and Comparative Examples are shown in Table 1 below.

<Synthesis method of titanium oxide C, F to H>
Titanium oxide (amorphous) was synthesized by hydrolyzing and polycondensing titanium tetraisopropoxide (TTIP), and crystallized by firing.
Specifically, it was synthesized through the following steps (1) to (6).
(1) Using TTIP (manufactured by Tokyo Kasei Kogyo Co., Ltd., product code: T0133), isopropanol (manufactured by Tokyo Kasei Kogyo Co., Ltd., purity 99.5% or more, product code: I0163) and ion-exchanged water, the following solution was prepared. A to C were produced.
Solution A: 35.6 parts by mass of TTIP, 200 parts by mass of isopropanol Solution B: 200 parts by mass of isopropanol, 6.3 parts by mass of ion-exchanged water Solution C: 200 parts by mass of isopropanol, 24.4 parts by mass of ion-exchanged water (2) Teflon While stirring Solution A with a (registered trademark) stirring blade, Solution B was slowly added dropwise, and stirring was continued for 10 minutes.
(3) Solution C was slowly added dropwise to the mixture of solution A and solution B obtained in (2) above, stirring was continued for 1 minute, and then allowed to stand at room temperature for 24 hours.
(4) The precipitate was separated into solid and liquid using a membrane filter (manufactured by Advantech, material: cellulose acetate).
(5) After washing with isopropanol, it was dried at 100° C. for 5 hours to obtain titanium oxide (amorphous).
(6) Fired in a muffle furnace to crystallize titanium oxide.
The firing was carried out at the temperature shown in the table, at a heating rate of 10° C./min, and for 2 hours after heating.

[Examples 1-1 to 1-12, Comparative Examples 1-1 to 1-3]
Broadleaf bleached kraft pulp (LBKP) was beaten with a double disc refiner so that the CSF was 450 mL to prepare a 3% by mass pulp slurry.
After diluting by adding 0.5 parts by mass of sulfuric acid to 100 parts by mass of pulp (solid content), the content of titanium oxide shown in Table 2 in the printing paper is equal to the content (mass%) shown in Table 2. Added so that Furthermore, 0.8 parts by mass of a polyepichlorohydrin wet paper strength agent WS4024 (manufactured by Seiko PMC Co., Ltd.) was added to 100 parts by mass of the pulp, and the mixture was formed into a sheet using a wet paper machine. An ultraviolet laser printing paper having the basis weight and thickness shown in 2 was prepared.

[Example 1-13]
Paper was made in the same manner as in Example 1-4, except that 30 parts of hardwood bleached kraft pulp (LBKP) and 70 parts of softwood bleached kraft pulp (NBKP) were mixed and beaten so that the CSF was 550 mL.

[Example 1-14]
Paper was made in the same manner as in Example 1-4, except that 100 parts of softwood bleached kraft pulp (NBKP) was beaten to a CSF of 580 mL.

[Example 1-15]
70 parts of the same hardwood bleached kraft pulp (LBKP) as in Example 1-4 and 30 parts of powder pulp made from the LBKP (procedure below) were used, except that they were mixed and beaten so that the CSF was 400 mL. , Paper was made in the same manner as in Example 1-4.
<Powder pulp>
The powder pulp was produced by mechanically crushing a dry sheet of bleached hardwood kraft pulp (LBKP) using a cutter mill (manufactured by Horai Co., Ltd., HA8 2542 30E, screen 0.24 mm).

[Example 1-16]
The hardwood bleached kraft pulp (LBKP) of Example 1-1 was milled using a pulp machine and dried to obtain dry pulp. Paper was made in the same manner as in Example 1-4, except that the dry pulp was re-disintegrated and beaten to a disintegration freeness of 550 mL.

[Examples 2-1 to 2-16, Comparative Examples 2-1 to 2-3]
<Manufacture of paper base material>
Paper base materials were produced in the same manner as in Examples 1-1 to 1-16 and Comparative Examples 1-1 to 1-3, respectively.

<Formation of sealant layer>
PE (low-density polyethylene, manufactured by Japan Polyethylene Co., Ltd., Novatec (registered trademark) LD LC522) was introduced into a single screw extruder (manufactured by Toyo Seiki Seisakusho Co., Ltd., D2025), and one side of the paper base material was coated with resin. After extrusion lamination (melt lamination) to a thickness of 15 μm, the sheets were rapidly cooled while being sandwiched between cooling rolls whose temperature was adjusted to 20° C., and a sealant layer was provided to obtain ultraviolet laser printing paper. Note that the melting temperature of the resin in the extrusion laminate was 320°C. Note that a sealant layer was provided on the less smooth surface of the paper base material.

[Example 2-17]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of sealant layer>
On the surface of a PE film (linear low-density polyethylene film (LLDPE), manufactured by Futamura Chemical Co., Ltd., LL-XLTN, thickness 25 μm), 10 parts of isocyanate adhesive (manufactured by DIC Corporation, Dick Dry LX-500) was applied. Then, 5 g/m ^{2 of 5 g/m 2} of DIC Dry KW-75 (mixed with 1 part of Dick Dry KW-75 manufactured by DIC Corporation) was applied, and the paper was bonded to a paper base material to obtain an ultraviolet laser printing paper.

[Example 2-18]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of sealant layer>
A sealant layer was formed in the same manner as in Example 2-4, except that PE was changed to PP (polypropylene, manufactured by Mitsubishi Chemical Corporation, Novatec PP MA-3) and the melting temperature was set to 330°C, and then UV laser printing was performed. I got the paper.

[Example 2-19]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of sealant layer>
A sealant layer was formed in the same manner as in Example 2-17, except that the PE film was changed to a CPP film (unoriented polypropylene film, manufactured by Futamura Chemical Co., Ltd., FHK2-L, thickness 25 μm), and ultraviolet laser printing was performed. I got the paper. The film was a laminated film of CoPP (copolymerized polypropylene)/CoPP (copolymerized polypropylene)/special PP, and the CoPP surface, which was the corona-treated surface, was placed on the paper base material side.

[Example 2-20]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of sealant layer>
Add water to a water-based heat sealing agent (ethylene-acrylic acid copolymer (Et-AA in the table), manufactured by Michaelman, MFHS1279, solid content concentration 42%) to dilute to 20% solid content, and then Apply the sealant to the opposite side of the base material from the side with the printed layer using a Mayer bar to a coating amount (solid content) of 5 g/ ^m2 , dry at 120°C for 60 seconds, and apply the sealant. A layer was formed to obtain an ultraviolet laser printing paper.

[Example 2-21]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of sealant layer>
A water-based heat sealing agent (ethylene-methacrylic acid copolymer (Et-MAA in the table), manufactured by Mitsui Chemicals, Inc., Chemipearl S-300, solid content concentration 35%) was used after adjusting the solid content concentration to 20%. Except for this, a sealant layer was formed in the same manner as in Example 2-20, and an ultraviolet laser printing paper was obtained.

[Example 2-22]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of sealant layer>
A water-based heat sealing agent (styrene-acrylic acid copolymer (St-AA in the table), manufactured by Seiko PMC Co., Ltd., SEIKOAT RE-2016, solid content concentration 35%) was used after adjusting the solid content concentration to 20%. Except for this, a sealant layer was formed in the same manner as in Example 2-20, and an ultraviolet laser printing paper was obtained.

[Example 2-23]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of barrier layer>
EVOH (ethylene-vinyl alcohol copolymer, manufactured by Kuraray Co., Ltd., EVAL E105B) was charged into a single screw extruder (manufactured by Toyo Seiki Seisakusho Co., Ltd., D2025), and the thickness of the resin was added to one side of the paper base material. After extrusion lamination (melt lamination) so that the thickness was 15 μm, the material was rapidly cooled while being sandwiched between cooling rolls whose temperature was adjusted to 20° C. to form a barrier layer. Note that the melting temperature of the resin in the extrusion laminate was 215°C.
<Formation of sealant layer>
A sealant layer was provided in the same manner as in Example 2-4 to obtain ultraviolet laser printing paper.

[Example 2-24]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of barrier layer>
An aqueous dispersion of a layered inorganic compound (layered inorganic compound = synthetic mica (swellable Mica, average length: 6.3 μm, aspect ratio: approximately 1000, thickness: approximately 5 nm), solid content concentration 6% by mass, manufactured by Topy Industries, Ltd., NTO-05) was added, and further diluted to this. Water was added to make the solid content concentration 10% by mass to obtain a barrier layer coating liquid. The barrier layer coating solution was applied using a Meyer bar so that the coating amount was 2.0 g/m ² , and then dried in a hot air dryer at 120°C for 1 minute to form a barrier layer. Formed.
<Formation of sealant layer>
A sealant layer was provided in the same manner as in Example 2-20 to obtain ultraviolet laser printing paper.

[Example 2-25]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of barrier layer>
Aqueous dispersion of layered inorganic compound (layered inorganic compound = synthetic mica (swellable mica, average length: 6.3 μm, aspect ratio: approximately 1000, thickness: approximately 5 nm), solid content concentration 6% by mass, Topy Industries, Ltd. company, NTO-05), urethane emulsion (solid concentration 30% by mass, glass transition temperature 130°C, oxygen permeability when forming a 25μm thick sheet 2.0mL/( ^m2・day・atm), Mitsui Chemicals) Takelac WPB-341 (manufactured by Co., Ltd.) was added so that the solid content mass ratio (layered inorganic compound: urethane resin) was 2:10, and the mixture was stirred. Furthermore, dilution water was added so that the solid content concentration was 20% by mass to obtain a barrier layer coating solution. The barrier layer coating solution was applied with a Mayer bar so that the coating amount of the barrier layer was 2.0 g/m ² , and then dried in a hot air dryer at 120°C for 1 minute to form a barrier layer. formed a layer.
<Formation of sealant layer>
A sealant layer was provided in the same manner as in Example 2-20 to obtain ultraviolet laser printing paper.

[Example 2-26]
<Manufacture of paper base material>
A paper base material was produced in the same manner as in Example 1-4.
<Formation of barrier layer>
Aluminum vapor deposited PP film (base material = CPP (unstretched polypropylene film), manufactured by Mitsui Chemicals Tohcello Co., Ltd., product name: ML, thickness 20 μm, water vapor permeability 0.2 g/m ² day, oxygen permeability 50 mL/m Apply an isocyanate adhesive (10 parts of Dick Dry LX-500, manufactured by DIC ^Corporation , and 1 part of Dick Dry KW-75, manufactured by DIC Corporation) to the surface of the PP film side of the 2-day ATM). After applying 5 g/m ² , it was laminated to one side of the paper base material.
<Formation of sealant layer>
A sealant layer was formed in the same manner as in Example 2-4 to obtain ultraviolet laser printing paper.

[Example 2-27]
In forming the barrier layer, an aluminum vapor-deposited PET film (base material = PET (polyethylene terephthalate), manufactured by Mitsui Chemicals Tohcello Co., Ltd., product name: ML, thickness 12 μm, water vapor permeability 1 g/m2) was used instead of the aluminum vapor-deposited ^PP film. Ultraviolet laser printing paper was obtained in the same manner as in Example 2-26, except for using an oxygen permeability of 10 mL/m ² ·day · atm). Note that the adhesive was applied to the base material (PET) side.

[Example 2-28]
In forming the barrier layer, a silica-deposited PP film (base material = PP, manufactured by Toppan Printing Co., Ltd., product name: GL-LP, thickness 17 μm, water vapor permeability 0.5 g/m ² . Ultraviolet laser printing paper was obtained in the same manner as in Example 2-26, except that an oxygen permeability of 1 mL/m ² ·day · atm) was used. Note that the adhesive was applied to the base material (PP) side.

[Example 2-29]
In forming the barrier layer, silica-deposited PET film (base material = PET, manufactured by Toppan Printing Co., Ltd., product name: GL-AE, thickness 12 μm, vapor-deposited layer thickness 400 nm, water vapor permeability) was used instead of aluminum-deposited PP film. Ultraviolet laser printing paper was obtained in the same manner as in Example 2-26, except that an oxygen permeability of 0.6 g/m ² ·day and an oxygen permeability of 0.2 mL/m ² ·day ·atm) were used. Note that the adhesive was applied to the base material (PET) side.

[Example 2-30]
In forming the barrier layer, an alumina vapor-deposited PET film (base material = PET, manufactured by Mitsui Chemicals Tohcello Co., Ltd., product name: TL, thickness 12 μm, water vapor permeability 1.5 g/m ^2.day ) was used instead of the aluminum vapor-deposited PP film. An ultraviolet laser printing paper was obtained in the same manner as in Example 2-26, except that an oxygen permeability of 15 mL/m ² ·day · atm) was used. Note that the adhesive was applied to the base material (PET) side.

[Example 2-31]
In forming the barrier layer, a PET film coated with PVDC (polyvinylidene chloride) (manufactured by Mitsui Chemicals Tohcello Co., Ltd., product name: V Barrier, thickness 12 μm, water vapor permeability 0.2 g/m) was used instead of the aluminum vapor-deposited PP film. Ultraviolet laser printing paper was obtained in the same manner as in Example 2-26, except that ^2.day and oxygen permeability of 0.8 mL/m ^2.day.atm ) were used. Note that the adhesive was applied to the base material (PET) side.

[Reference example 2-1]
An ultraviolet laser printing paper was obtained in the same manner as in Example 2-4 except that a sealant layer was not formed.

[Measurement/Evaluation]
The following measurements and evaluations were performed on the ultraviolet laser printing papers and various raw materials obtained in Examples and Comparative Examples.

[Average particle size of titanium oxide]
The average particle diameter of titanium oxide was measured by the following method.
The paper base material was scraped off from the ultraviolet laser printing paper obtained in Examples and Comparative Examples using an industrial razor (manufactured by Feather Safety Razor Co., Ltd., product number: 099769), and the collected paper base material was used as a sample in a muffle furnace. It was calculated from an SEM image (secondary electron image) obtained from a scanning electron microscope (SEM, manufactured by Hitachi High-Technology Corporation, SU7000, etc.) of the ash obtained by combustion. The ash content was obtained by burning at 450° C. using a muffle furnace (manufactured by Yamato Scientific Co., Ltd., model number FO300) and incinerating it.
In addition, if it does not have a layer other than the paper base material, the ash obtained by burning the ultraviolet laser printing paper itself in the same way and ashing it without scraping off the paper base material and collecting it. It may be calculated from the SEM image obtained from .
Next, the slurry was dispersed in ethanol for 5 minutes using an ultrasonic cleaner (such as LSC-63 manufactured by As One Co., Ltd.) to obtain a 0.1% by mass slurry, and then 0.1 mL was cast onto an aluminum plate and heated at 100°C. A sample for measurement was prepared by drying the sample. Each aluminum plate was subjected to observation using a scanning electron microscope (SEM, manufactured by Hitachi High-Tech Corporation, SU7000, etc.), and particles that could be clearly distinguished from adjacent particles were visually selected, and the major and minor diameters of each particle were determined. Particle diameter was calculated from the geometric mean. At this time, if primary particles and secondary particles in an agglomerated state are mixed but can be clearly distinguished, each is counted as one particle, 100 particles are selected at random, and the did. In addition, when particles other than titanium oxide were included, particles containing the titanium element were measured using an energy dispersive X-ray analyzer (manufactured by Horiba, Ltd., EMAX, etc.) attached to the SEM.
In addition, in the case of needle-like particles, the major axis was measured for 100 particles, and the average was taken as the average particle diameter.

[Crystallite size calculation method]
<Measurement sample preparation method>
The paper base material was scraped off from the ultraviolet laser printing paper obtained in Examples and Comparative Examples using an industrial razor (manufactured by Feather Safety Razor Co., Ltd., product number: 099769), and the collected paper base material was used as a sample in a muffle furnace. It was calculated from an SEM image (secondary electron image) obtained from a scanning electron microscope (SEM, manufactured by Hitachi High-Technology Corporation, SU7000, etc.) of the ash obtained by combustion. The ash content was obtained by burning at 450° C. using a muffle furnace (manufactured by Yamato Scientific Co., Ltd., model number FO300) and incinerating it.
In addition, when it does not have a layer other than the paper base material, the ultraviolet laser printing paper itself may be similarly fired and incinerated to obtain ash content without scraping off and collecting the paper base material.

<Measurement by X-ray diffraction method>
The test sample obtained by incineration was filled into a sample holder and measured using a high-speed detector. During filling, the sample measurement surface was adjusted to be at the same height as the edge of the sample holder by using a height adjustment jig as appropriate depending on the sample amount.
(Measurement condition)
X-ray diffraction device: RINT-Ultima III manufactured by Rigaku Co., Ltd.
Voltage: 40kV
Current: 40mA
Optical system: parallel beam (CBO)
Detector: High-speed detector D/teX Ultra 2 manufactured by Rigaku Co., Ltd.
Goniometer: Ultima III Horizontal goniometer Tube: Cu
Wavelength: 1.541 Å (Kα1)
Scan mode: CONTINUOUS
Scan speed: 1.0000deg/min
Step width: 0.0500deg
Scan axis: 2Theta/Theta
Scan range: 5.0000~60.0000deg
Incidence slit: 1.0mm
Longitudinal limit slit: 10mm
Light receiving slit 1: Open Light receiving slit 2: Open Sample holder: ASC-6 sample holder (product number 2455E442)
Material: Aluminum Dimensions: φ23mm x 2.0mm
Holder height adjustment jig: Transparent disc-shaped plate (homemade)
Material: Polymethyl acrylate Dimensions: φ23mm x 0.8mm

<Processing of data obtained by X-ray diffraction>
Background processing and profile fitting processing were performed on the obtained diffraction profile using integrated powder X-ray analysis software (manufactured by Rigaku Co., Ltd., PDXL2).
All data processing settings were set to the default settings of the software unless otherwise specified.
The crystal phase was identified based on the information on the peak position and peak intensity of the diffraction profile based on a database (ICDD).

<Calculation of crystallite size based on data obtained by X-ray diffraction>
The half-width at half maximum (FWHM) of the strongest diffraction line obtained from the diffraction profile after data processing and the Bragg angle (θ) were substituted into the Scherrer equation to calculate the crystallite size.
The X-ray diffraction peaks of titanium oxide used in the calculation are as follows.
Anatase: 101 planes Rutile: 110 planes The Scherrer formula is as follows.

D: Crystallite size (nm)
K: Scherrer constant λ: X-ray wavelength (nm)
B:FWHM (rad)
θ: Bragg angle (rad)
The value of K is 0.89, B is the FWHM value obtained by measurement, the value of λ is 0.154, and the value of θ is the actual measurement of the maximum intensity derived from the 101 plane for anatase and the 110 plane for rutile. value.

[CSF]
The Canadian standard freeness (CSF) of the raw material pulp was measured in accordance with JIS P 8121-2:2012.

[Basic weight of paper base material]
If the obtained ultraviolet laser printing paper has layers other than the paper base material, as a pretreatment, layers other than the paper base material, such as a sealant layer, barrier layer, and resin layer, are removed under a microscope. While confirming the boundary, it was removed by grinding using a grinding device (manufactured by Sagawa Seisakusho Co., Ltd., grindstone size: φ50.8 x 12.7 mm).
Next, if the printing paper has a sealant layer, barrier layer, resin layer, etc. provided by coating, some of these layers are immersed in the paper base material, so the printing paper that has undergone the above pretreatment is It was immersed in xylene at ℃ to elute the resin content.
The obtained paper base material was conditioned for one day in an environment of 23° C. and 50% humidity. The basis weight of the paper base material of the sample after humidity conditioning was measured in accordance with JIS P 8124:2011.

[Thickness of paper base material]
The thickness of the paper base material was measured in accordance with JIS P 8118:2014. The thicknesses of the barrier layer, heat seal layer, resin layer, etc. were calculated from the SEM image as described below, and were subtracted from the values measured in accordance with JIS P 8118:2014.

[Length-weighted average fiber length, fiber width, and fine fiber content of pulp fibers constituting the paper base material]
The length-weighted average fiber length, fiber width, and fine fiber content of the pulp constituting the paper base material were measured by the following methods.
The printing media of Examples and Comparative Examples were cut into 4 cm square pieces, about 50 times the mass of ion-exchanged water was added thereto, and then immersed in ion-exchanged water for 24 hours.
After soaking for 24 hours, the pulp was disintegrated into fibers using a standard disintegrator (manufactured by Kumagai Riki Kogyo Co., Ltd.) until there were no undisintegrated fibers. If the resin layer, sealant layer, barrier layer, etc. The "length-weighted average fiber length (ISO),""fine fiber content," and "fiber width" were measured using a fiber optic (with 3000 ml, manufactured by Valmet).
Note that "length-weighted average fiber length (ISO)" is a length-weighted average fiber length calculated by selecting fibers with a length of 0.2 mm or more and 7.6 mm or less. Moreover, "amount of fine fibers" is the number ratio of fine fibers having a fiber width of 75 μm or less and a length of 0.08 mm or more and 0.20 mm or less in the disintegrated pulp fibers. "Fiber width" is a length-weighted average fiber width calculated by selecting fibers with a width of 10 μm or more and 75 μm or less.

[Titanium oxide content]
<Measurement of moisture in paper base material>
The moisture content of the paper base material was measured according to JIS P 8203:2010 (ISO 638:2008).
<Preparation of test piece>
From the obtained ultraviolet laser printing paper, as a pretreatment, while checking the layer boundaries under a microscope, using a grinding device (manufactured by Sagawa Seisakusho Co., Ltd., grinding wheel size φ50.8 x 12.7 mm), paper base material The other layers (sealant layer, barrier layer, and resin layer) were removed by grinding.
The obtained sample was subjected to humidity conditioning according to the method of JIS P 8111:1998, and then cut into an appropriate size to prepare a sample (test piece), and the cut out area and mass were recorded.

<Dissolution of test piece>
A mixed solvent of nitric acid:hydrofluoric acid=50:5 (volume%) and the test piece were put into a Teflon (registered trademark) container of an autoclave device (manufactured by CEM Japan, MARS5), and autoclaved at 210°C for 120 minutes. and dissolved the test piece. The mass of the test piece may be changed as appropriate, and if the test piece remains undissolved, the ratio of nitric acid and hydrofluoric acid, treatment temperature, treatment time, etc. may be changed as appropriate.
After dissolving the test piece, the volume was accurately adjusted using ultrapure water.

<Measurement of titanium oxide amount in solution>
(1) The ICP device and measurement conditions are as follows.
ICP device: ICP-OEC device (manufactured by Rigaku Co., Ltd., CIROS1-20)
Measurement condition:
・Carrier gas: Argon gas ・Argon gas flow rate 0.9L/min
・Plasma gas flow rate 14L/min
・Plasma output 1400W
・Pump rotation speed: 2
・Measurement wavelength Ti: 334.941nm
(2) Creating a calibration curve Accurately measure a general-purpose mixed standard solution (manufactured by SPEX, XSTC-622B) to the following concentration, and test it under the above measurement conditions, which corresponds to the emission wavelength of titanium atoms. The intensity at 334.941 nm was measured.
・Concentration for creating a calibration curve: 0ppm, 0.01ppm, 0.05ppm, 0.1ppm, 0.5ppm, 1.0ppm, 3.0ppm, 5.0ppm
(3) Measurement of titanium oxide content in solution The solution in which the test piece was dissolved was diluted with ultrapure water so that it fell within the above calibration curve, and was subjected to ICP measurement.
(4) Titanium oxide content calculation method Titanium oxide content was calculated using the following formula. Note that the molecular weight of titanium oxide divided by the atomic weight of titanium is approximately 1.669.
Titanium oxide content (g/m ² ) = ICP measurement concentration (ppm) x dilution ratio x constant volume (L) x 1.669 x 1000 ÷ area (m ² )
Titanium oxide content (mass%) = ICP measurement concentration (ppm) x dilution ratio x constant volume (L) x 1.669 ÷ test piece mass (mg) x (1-moisture content) x 100

[Thickness of sealant layer]
The thickness of the sealant layer was measured from image data obtained from a scanning electron microscope.
(1) Preparation of measurement sample The sample was embedded in a photocurable resin (manufactured by Toagosei Co., Ltd., D-800), and the cross section of the printing paper was sectioned using an ultramicrotome. A diamond knife was used for cutting, and cutting was performed at room temperature.
Gold was deposited to a thickness of about 20 nm on the cut cross section, and the sample was subjected to measurement using a scanning electron microscope.
(2) Measuring device/conditions Measuring device: S-3600 (manufactured by Hitachi High-Tech Corporation)
Measurement conditions: 2000x magnification Although the type of scanning microscope is not limited to the above, a type of device with a scale bar displayed was used.
When the sealant layer was thin, an appropriate magnification was selected to acquire image data.
(3) Measurement method Image data was acquired using a scanning electron microscope at a magnification of 2000 times. After printing the obtained image data on printing paper, measure the thickness of the target sealant layer (the length of the boundary from the boundary with other layers) with a ruler, and compare it with the scale bar to determine the actual sealant layer ( The thickness of the coated layer or laminate layer was measured. Image data of 5 randomly selected locations were acquired from one measurement sample, and from the image data of 1 location, the thickness of the location where the sealant layer was the thickest and the location where the sealant layer was the thinnest was measured, and a total of 10 locations were measured. The average was taken as the thickness of the sealant layer. Note that the observation magnification may be changed depending on the thickness of the sealant layer to be observed.
Note that when the paper base material further has a resin layer on the opposite side to the side on which the sealant layer is provided, the thickness of the resin layer can be measured by the same method. Further, the thickness of the barrier layer can also be measured in the same manner.

[Measurement of Raman spectrum]
The Raman spectrum was measured by the following method. In this example, the measurement of the Raman spectrum was performed on a printed matter obtained with the sharpness of one printing point, which will be described later.
<Measurement conditions>
The measurement conditions for Raman spectra are as follows. However, if the laser used for measurement causes damage to the printed matter, the fluorescence is strong, or the peak is weak, etc., please adjust the laser output, irradiation time, etc. as appropriate. measurement conditions can be changed. However, the Raman intensities of the printed area and non-printed area are measured under the same conditions.
・Equipment: inVia Raman microscope QUONTOR manufactured by Renishaw
・Excitation laser: 532nm
・Laser power: 50mW (at 100% output)
・Laser output: 50%
・Measurement mode: Confocal mode ・Irradiation time: 0.5 sec
・Number of integration: 10 times ・Laser spot diameter: 2.5 μm
・Objective lens: 20x

<Measurement method>
Measurement was performed using the following method.
(1) Calibration of the Raman shift position was performed using a standard sample (single crystal silicon, manufactured by Renishaw) (520.5 cm ⁻¹ of single crystal silicon).
(2) A sheet-shaped sample was placed on a sample stage. Holders were installed as necessary to keep the sheet flat.
(3) Observation was performed with the device focused (the simulated laser was set to have the smallest focus). When measuring the printed area, the blackest part that could be visually confirmed was placed in the center of the guide displayed during measurement. When measuring the non-printing area, it was measured at a distance of 300 μm or more from the printing area.
(4) The obtained Raman spectrum was subjected to baseline correction (intelligent correction) using processing software (manufactured by Renishaw, Wire 5.2) attached to the apparatus. The baseline was corrected using polynomial 11 of the processing software.
(5) The maximum value (maximum intensity) in the wavenumber range of 447±10 cm ⁻¹ for rutile titanium oxide and 516±10 cm ⁻¹ for anatase titanium oxide was read, and the Raman intensity ratio was calculated using the following formula.
Raman intensity ratio = Maximum intensity of printed area ÷ Maximum intensity of non-printed area (6) Measurements were taken at 10 locations each for the printed area (printed area) and non-printed area (non-printed area), and the average value was taken as the measurement result. .
From the viewpoint of suppressing variations in measured values, it is preferable to measure the Raman intensity count of the printed area within a range of 10,000 or less. Therefore, the measurement conditions were appropriately changed so that the Raman intensity count of the printed area was within 10,000. In addition, measurements were performed 10 times under the following measurement conditions, and values that deviated by more than the average value ± 2 SD (standard deviation) were excluded, and the values were averaged again to obtain the average value of the Raman intensity.
The Raman intensity ratio was evaluated based on the following criteria.
A: Raman intensity ratio is 0.3 or less B: Raman intensity ratio is more than 0.3 and 0.7 or less C: Raman intensity ratio is more than 0.7

[Clearness of one printing point]
<Laser printing method>
A 10 mm square was printed on the sample surface of the printing paper obtained in Examples and Comparative Examples using an ultraviolet laser irradiation machine (manufacturer name: Keyence Corporation, model number: MD-U1020C).
(Printing conditions)
Wavelength: 355nm
Output: 80% (2.5W at 100% output)
Frequency: 40kHz
Focal length: 300mm (focusing is performed using the height correction included with the device)
Spot diameter: 40μm (when focusing)
Filling interval: 0.3mm
Scan speed: 5000mm/sec
Spot variable: 100

<Clarity evaluation>
A depth composite image of the vicinity of the printed area to be evaluated was obtained using a digital microscope (manufacturer name: Keyence Corporation, model number: VHX-8000).
A depth composite image is an image obtained by acquiring a plurality of images by changing the focal length, extracting in-focus portions from each image, and constructing a single image. Depth composite images were acquired using the live depth composite function installed in a digital microscope.
Thereafter, the brightness extraction mode of the automatic area measurement function was used to measure the area of the area darker than the threshold value in the printed area. The brightness extraction mode is a mode that hierarchizes the brightness level of an image from -255 to 255 and extracts an area above or below an arbitrary threshold value.
Regarding the printed portion, it was decided that the larger the number of areas where the luminance level was lower than the threshold value, the more the area was considered to be a "darker printed character."
(Settings when shooting images)
Shutter speed: Auto mode (setting value 70)
Gain: 0dB
Magnification: 400x Lighting: Ring lighting (brightness extraction mode setting)
Magnification when acquiring depth composite images: 400x Illumination: 100% coaxial epi-illumination
Shutter speed: auto mode 70
Gain: 0dB
Threshold: -7
Extraction area: Inside a circle with a radius of 60 μm from the center of the printed area (criteria for evaluating the darkness of the printed area)
A: The area of the area with a brightness level lower than -7 is 70% or more of the extraction area B: The area of the area with a brightness level lower than -7 is 65% or more and less than 70% of the extraction area C: The brightness level is lower than -7 The area of the area is 45% or more and less than 65% of the extraction area D: The area of the area with a brightness level lower than -7 is less than 45% of the extraction area

[Printing uniformity]
A 10 mm square was printed on the sample surface using an ultraviolet laser irradiation machine (manufacturer name: Keyence Corporation, model number: MD-U1020C) on the ultraviolet laser printing paper obtained in Examples and Comparative Examples.
(Printing conditions)
Wavelength: 355nm
Output: 80% (2.5W at 100% output)
Frequency: 40kHz
Focal length: 300mm (focusing is performed using the height correction included with the device)
Spot diameter: 40μm (when focusing)
Filling interval (line pitch): 0.05mm
Scan speed 3000mm/sec
Spot variable: -100

(Printing uniformity evaluation)
100 squares were printed, and printing uniformity was evaluated according to the following criteria based on the number of squares in which a visually observable shading difference (print non-uniformity) existed.
A: For 100 squares, the number of squares with a difference in shading is less than 3 B: For 100 squares, the number of squares with a difference in shading is 3 or more and less than 5 C: For 100 squares, the number of squares with a difference in shading is less than 3 The number of squares with a difference is 5 or more and less than 10 D: The number of squares with a difference in shade is 10 or more per 100 squares

[Fuming]
When evaluating printing uniformity, smoke generation when a 10 mm x 10 mm square was printed on the sample surface by ultraviolet laser irradiation was evaluated using the following criteria.
(Judgment criteria)
A: Smoke cannot be visually confirmed, or smoke can be faintly confirmed, but it is very rare. B: Smoke can be visually confirmed, but the amount of smoke is small. C: Smoke can be visually confirmed, but it does not affect printing. Not so much D: Smoke can be easily confirmed visually, and the amount of smoke is large enough to scatter the ultraviolet laser light and affect printing.

[Water vapor barrier property]
The water vapor barrier properties of the printing papers obtained in Examples 2-1 to 2-31, Comparative Examples 2-1 to 2-3, and Reference Example 2-1 in which sealant layers were provided were evaluated. Measurement was performed with the sealant layer on the inside in accordance with JIS-Z-0208:1976 (cup method) method B (40°C ± 0.5°C, relative humidity 90% ± 2%).
The water vapor barrier property was evaluated using the following evaluation criteria.
(Evaluation criteria for water vapor barrier properties)
A: Water vapor permeability is 30 g/m ² ·day or less B: Water vapor permeability exceeds 30 g/m ² ·day and is 40 g/m ² ·day or less C: Water vapor permeability exceeds 40 g/m ² ·day 50g/ ^m2・day or less D: Water vapor permeability exceeds 50g/ ^m2・day

Further, laser irradiation was performed under the following conditions, and the water vapor permeability of the ultraviolet laser printed matter after laser irradiation was similarly measured. Note that for Reference Example 2-1, the evaluation of the water vapor barrier property before ultraviolet laser irradiation was D, so it was not measured.
<Laser irradiation>
The ultraviolet laser printing paper obtained in Examples 2-1 to 2-31 and Comparative Examples 2-1 to 2-3 was treated with an ultraviolet laser irradiation machine (manufacturer name: Keyence Corporation, model number: MD-U1020C). Then, a 10 cm square was printed on the sample surface (printed layer side) under the conditions described below.
・Printing conditions Wavelength: 355nm
Output: 80% (2.5W at 100% output)
Frequency: 40kHz
Focal length: 300mm (focusing is performed using the height correction included with the device)
Spot diameter: 40μm (when focusing)
Filling interval: 0.04mm
Scan speed 1000mm/sec
Spot variable: 0

[Oxygen barrier property]
Oxygen permeation of the ultraviolet laser printing papers of Examples 2-23 to 2-31 was measured using an oxygen permeability measuring device (OX-TRAN2/22, manufactured by MOCON) under conditions of a temperature of 23°C and a relative humidity of 85%. The degree was measured.
Specifically, the oxygen permeability of the laminated sheet was measured at a temperature of 23° C. and a relative humidity of 85% in accordance with JIS K7126-2:2006.
The lower the oxygen permeability value, the better the oxygen barrier property.
Oxygen barrier properties were evaluated using the following evaluation criteria.
(Oxygen barrier evaluation criteria)
A: Oxygen permeability is 3.0 mL/m ² ·day · atm or less B: Oxygen permeability exceeds 3.0 mL/m ² ·day · atm and is below 5.0 mL/m ² ·day · atm C: Oxygen Permeability exceeds 5.0 mL/m ² ·day · atm and is below 15 mL/m ² ·day · atm D: Oxygen permeability exceeds 15 mL/m ² ·day · atm

Further, laser irradiation was performed under the following conditions, and the oxygen permeability of the ultraviolet laser printed matter after laser irradiation was similarly measured.
<Laser irradiation>
The ultraviolet laser printing paper obtained in Examples 2-1 to 2-31 and Comparative Examples 2-1 to 2-3 was treated with an ultraviolet laser irradiation machine (manufacturer name: Keyence Corporation, model number: MD-U1020C). Then, a 10 cm square was printed on the sample surface (printed layer side) under the conditions described below.
・Printing conditions Wavelength: 355nm
Output: 80% (2.5W at 100% output)
Frequency: 40kHz
Focal length: 300mm (focusing is performed using the height correction included with the device)
Spot diameter: 40μm (when focusing)
Filling interval: 0.04mm
Scan speed 1000mm/sec
Spot variable: 0

[Barrier property reduction rate after ultraviolet laser irradiation (barrier property reduction rate)]
From the water vapor permeability and oxygen permeability before and after ultraviolet laser irradiation, the reduction in barrier properties (barrier property reduction rate) due to ultraviolet laser irradiation was evaluated using the following evaluation criteria.
(Evaluation criteria for barrier property reduction rate)
A: The rate of decrease (reduction rate) in water vapor permeability and oxygen permeability is 5.0% or less B: The rate of decrease (reduction rate) in water vapor permeability and/or oxygen permeability exceeds 5.0% Note that water vapor The rate of decrease in transmittance is calculated as follows.
Reduction rate of water vapor permeability = (Water vapor permeability after ultraviolet laser irradiation (g/m ² ·day) - Water vapor permeability before ultraviolet laser irradiation (g/m ² ·day)) / Water vapor permeation before ultraviolet laser irradiation degree (g/ ^m2・day)×100
Similarly, the rate of decrease in oxygen permeability is calculated as follows.
Reduction rate of oxygen permeability = (oxygen permeability after ultraviolet laser irradiation (mL/m ² ·day · atm) - oxygen permeability before ultraviolet laser irradiation (mL/m ² ·day · atm)) / ultraviolet laser irradiation Previous oxygen permeability (mL/ ^m2・day・atm)×100

[Heat seal peel strength and heat seal peel strength reduction rate (peel strength reduction rate)]
In Examples 2-1 to 2-31, Comparative Examples 2-1 to 2-3, and Reference Example 2-1, a set of two sheets of ultraviolet laser printing paper was stacked so that the sealant layers faced each other, and a heat seal tester was used. (manufactured by Tester Sangyo, TP-701-B) under the conditions of 160° C., 0.2 MPa, and 1 second. The heat-sealed test piece was left standing in a room at a temperature of 23° C.±1° C. and a humidity of 50%±2% for 4 hours or more. Subsequently, the heat-sealed test piece was cut to a width of 15 mm, and was subjected to T-peeling at a tensile speed of 300 mm/min using a tensile testing machine, and the maximum load recorded was taken as the heat-sealing peel strength.
Heat seal peel strength was evaluated using the following evaluation criteria.
(Evaluation criteria for heat seal peel strength)
A: Heat seal peel strength is 10 N/15 mm or more B: Heat seal peel strength is 6.0 N/15 m or more and less than 10 N/15 mm C: Heat seal peel strength is 3.0 N/15 mm or more and less than 6.0 N/15 mm D: Heat Seal peel strength is less than 3.0N/15mm <Laser irradiation>
The ultraviolet laser printing paper obtained in Examples 2-1 to 2-31, Comparative Examples 2-1 to 2-3, and Reference Example 2-1 was exposed to an ultraviolet laser irradiation machine (manufacturer name: Keyence Corporation, model number: MD-U1020C) was used to print a 10 cm square on the sample surface (printing layer side) under the conditions described below.
・Printing conditions Wavelength: 355nm
Output: 80% (2.5W at 100% output)
Frequency: 40kHz
Focal length: 300mm (focusing is performed using the height correction included with the device)
Spot diameter: 40μm (when focusing)
Filling interval: 0.04mm
Scan speed 1000mm/sec
Spot variable: 0
(Evaluation criteria for heat seal peel strength reduction rate)
The rate of decrease in heat seal peel strength due to ultraviolet laser irradiation was evaluated based on the heat seal peel strength before and after ultraviolet laser irradiation using the following evaluation criteria. Note that for Comparative Example 2-4, the evaluation of the heat seal peel strength before UV laser irradiation was D, so it was not measured.
(Evaluation criteria for reduction rate of heat seal peel strength)
A: The rate of decrease (rate of decrease) in heat seal peel strength is 5.0% or less B: The rate of decrease (rate of decrease) in heat seal peel strength exceeds 5.0% The rate of decrease in heat seal peel strength is: It is calculated as follows.
Reduction rate of heat seal peel strength = (Heat seal peel strength before UV laser irradiation (N/15mm) - Heat seal peel strength after UV laser irradiation (N/15 mm)) / Heat seal peel strength before UV laser irradiation ( N/15mm)×100

As shown in Table 2, by directly printing with an ultraviolet laser on ultraviolet laser printing paper that contains more than a certain amount of titanium oxide and has a titanium oxide crystallite size of more than a certain value, each point is clearly printed. Printed matter with excellent properties was obtained.
In Example 1-6, in which titanium oxide having a relatively large crystallite size of 55.3 nm was used, a decrease in printing uniformity was observed, which was considered to be due to a decrease in dispersibility. In addition, in Example 1-8 in which the diffraction angle was 27.74° and titanium oxide with relatively low crystallinity was used, a slight decrease in print clarity from point to point was observed. Furthermore, in the printing paper of Example 1-14 in which the length-weighted average fiber length of the constituent pulp was 2.18 mm, a decrease in print clarity per point was observed, which was thought to be due to an increase in the voids between the fibers. It was done.
On the other hand, with the printing papers of Comparative Examples 1-1 and 1-2 in which titanium oxide having a crystalline size of less than 30 nm was used, printed matter was obtained with poor print clarity on a point-by-point basis. In addition, in the printing paper of Comparative Example 1-3, in which the content of titanium oxide is 0.1% by mass and less than 0.5% by mass, when irradiated with ultraviolet laser, the print clarity of each point was poor. It became a spot.

As shown in Table 3, by directly printing with an ultraviolet laser on ultraviolet laser printing paper that contains more than a certain amount of titanium oxide and the crystallite size of titanium oxide is more than a certain value, each point is clearly printed. Printed matter with excellent properties was obtained.
Furthermore, it had heat sealability and excellent water vapor barrier properties. Furthermore, the ultraviolet laser printing papers of Examples 2-23 to 2-31 on which barrier layers were formed had excellent oxygen barrier properties. Further, deterioration in barrier properties and heat sealability due to printing with an ultraviolet laser was suppressed.
In Example 2-6, in which titanium oxide having a relatively large crystallite size of 55.3 nm was used, a decrease in printing uniformity was observed, which was considered to be due to a decrease in dispersibility. In addition, in Example 2-8 in which the diffraction angle was 27.74° and titanium oxide with relatively low crystallinity was used, a slight decrease in print clarity from point to point was observed. Furthermore, in the printing paper of Example 2-14 in which the length-weighted average fiber length of the constituent pulp was 2.18 mm, a decrease in print clarity per point was observed, which was thought to be due to an increase in the voids between the fibers. It was done.
On the other hand, with the printing papers of Comparative Examples 2-1 and 2-2 in which titanium oxide having a crystalline size of less than 30 nm was used, printed matter was obtained with poor print clarity on a point-by-point basis. In addition, in the printing paper of Comparative Example 2-3, in which the content of titanium oxide is 0.1% by mass and less than 0.5% by mass, when irradiated with ultraviolet laser, the print clarity of each point was poor. It became a spot.
Furthermore, when the printing paper of Reference Example 2-1 which did not have a sealant layer was used, heat sealing properties and water vapor barrier properties were not obtained.

In the ultraviolet laser printing paper of the present invention, titanium oxide changes color by irradiation with ultraviolet laser, so that it is possible to provide printed matter with excellent visibility and excellent print clarity for each point. The ultraviolet laser printed paper and printed matter of the present invention are suitably applied to processed products such as packages (preferably food containers), labels, and adhesive tapes on which variable information such as dates and barcodes are printed. Furthermore, the method for producing printed matter of the present invention is suitably applied to printing variable information on packages, labels, adhesive tapes, and the like.

Claims

An ultraviolet laser printing paper having a paper base material internally doped with titanium oxide,
The content of titanium oxide in the paper base material is 0.5% by mass or more,
The crystallite size of the titanium oxide is 30 nm or more,
UV laser printing paper.
The ultraviolet laser printing paper according to claim 1, wherein the titanium oxide has a crystallite size of 53 nm or less.
The ultraviolet laser printing paper according to claim 1, wherein the titanium oxide is rutile-type titanium oxide, and the diffraction angle of the titanium oxide is 27.60° or less.
The ultraviolet laser printing paper according to claim 1, wherein the length-weighted average fiber length of the pulp constituting the paper base is 0.5 mm or more and 3.0 mm or less.
The ultraviolet laser printing paper according to claim 1, wherein the number ratio of fine fibers with a fiber length of 0.2 mm or less among the pulp fibers constituting the paper base material is 4% or more and 40% or less.
The ultraviolet laser printing paper according to claim 1, wherein the content of titanium oxide in the paper base material is 50% by mass or less.
The ultraviolet laser printing paper according to claim 1, which has a sealant layer on at least one surface of the paper base material.
The ultraviolet laser printing paper according to claim 7, further comprising a barrier layer between the paper base material and the sealant layer.
A printed matter obtained from the ultraviolet laser printing paper according to any one of claims 1 to 8, comprising:
The printed matter has at least a portion of a printed area containing discolored titanium oxide,
A printed matter in which the ratio of the Raman intensity derived from titanium oxide in the printed area to the Raman intensity derived from titanium oxide in the non-printed area is 0.70 or less.
A processed product made using the ultraviolet laser printing paper according to any one of claims 1 to 8.
A processed product made using the printed matter according to claim 9.
A step of printing by irradiating the ultraviolet laser printing paper according to any one of claims 1 to 8 with an ultraviolet laser to change color in the irradiated area,
Method of manufacturing printed matter.
The printing step is a step of irradiating an ultraviolet laser so that the ratio of the Raman intensity originating from titanium oxide in the printing area to the Raman intensity originating from titanium oxide in the non-printing area is 0.70 or less. The method for producing a printed matter according to claim 12.