JP2019052384A - Luminous paper and method for producing the same - Google Patents
Luminous paper and method for producing the same Download PDFInfo
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Abstract
Description
本発明は、蓄光性のある紙、いわゆる蓄光紙、及びその製造方法に関し、特に、蓄光性が高く、両面に蓄光性があり、更には印刷が可能な蓄光紙及びその製造方法に関する。 The present invention relates to a phosphorescent paper, a so-called phosphorescent paper, and a method for producing the same, and more particularly, to a phosphorescent paper having a high phosphorescent property, phosphorescent on both sides, and capable of printing, and a method for producing the same.
現在、蓄光性をもつ紙は、後工程で蓄光性顔料等を印刷、又はコーティング等の手法により蓄光性を付与することが一般的に行なわれている。
しかし、印刷によって蓄光性を付与する場合は、絵柄等部分的にしか付与できず、コーティング等により全面塗工すると紙のカールが問題となる。
そこで、原紙の抄紙段階で蓄光性顔料を抄きこむことでこれらを改善し、また表裏両面に安定的に蓄光性を得る方法が知られている(例えば、特許文献1)。
Currently, it is a common practice to impart a phosphorescent property to a paper having a phosphorescent property by printing or coating a phosphorescent pigment or the like in a subsequent process.
However, when the phosphorescent property is imparted by printing, it can be imparted only partially, such as a pattern, and paper curling becomes a problem when the entire surface is coated by coating or the like.
Therefore, a method is known in which these are improved by incorporating a luminous pigment at the paper making stage of the base paper, and the luminous properties are stably obtained on both the front and back surfaces (for example, Patent Document 1).
ところが、従来の蓄光性顔料を含む紙においては、高い蓄光性を得るために、蓄光性顔料の粒径を大きくすると、紙への蓄光性顔料の歩留まりが低く、結果として生産性が悪くなることがあった。一方、蓄光性の顔料の粒径を小さくすると、蓄光性(輝度)が低くなることがあった。
本発明は、上記のような事情に鑑みてなされたものであり、生産性が高く、蓄光性(輝度)が高い蓄光紙及びその製造方法を提供することを目的とする。
However, in paper containing conventional luminous pigments, if the particle size of the luminous pigment is increased in order to obtain high luminous properties, the yield of the luminous pigment on the paper is low, resulting in poor productivity. was there. On the other hand, when the particle size of the phosphorescent pigment is reduced, the phosphorescent property (luminance) may be lowered.
The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a phosphorescent paper having high productivity and high phosphorescence (luminance) and a method for producing the same.
上記課題を解決するために、本発明の一態様である蓄光紙は、パルプ材に繊維、蓄光性顔料、及び紙力増強剤を含有し、上記蓄光性顔料の粒径が20μm以上50μm以下であり、上記蓄光性顔料が上記パルプ材に対し35重量%以上55重量%以下含まれている。
上記課題を解決するために、本発明の他の態様である蓄光紙の製造方法は、蓄光性顔料、パルプ材、繊維、紙力増強剤、及び水を含んでスラリーを精製し、上記スラリーを抄紙して蓄光紙を作製する蓄光紙の製造方法であって、上記蓄光性顔料の粒径が20μm以上50μm以下であり、上記蓄光性顔料が上記スラリーに35重量%以上55重量%以下含まれている。
In order to solve the above-described problems, the phosphorescent paper which is one embodiment of the present invention contains fibers, phosphorescent pigments, and paper strength enhancers in a pulp material, and the particle diameter of the phosphorescent pigment is 20 μm or more and 50 μm or less. In addition, the phosphorescent pigment is contained in an amount of 35% by weight to 55% by weight with respect to the pulp material.
In order to solve the above-mentioned problems, a method for producing phosphorescent paper according to another aspect of the present invention includes a phosphorescent pigment, a pulp material, a fiber, a paper strength enhancer, and water. A method for producing phosphorescent paper by making paper and producing phosphorescent paper, wherein the particle diameter of the phosphorescent pigment is 20 μm or more and 50 μm or less, and the phosphorescent pigment is contained in the slurry by 35 wt% or more and 55 wt% or less. ing.
本発明の一態様によれば、生産性が高く、蓄光性(輝度)が高い蓄光紙及びその製造方法を提供することができる。 According to one embodiment of the present invention, it is possible to provide a phosphorescent paper with high productivity and high phosphorescence (luminance) and a method for manufacturing the same.
次に、本発明の一実施形態について図面を参照して説明する。
ここで、以下の図面の記載において、同一又は類似の部分には同一又は類似の符号を付している。ただし、図面は模式的なものであり、厚みと平面寸法との関係、各層の厚みの比率等は現実のものとは異なることがあることに留意すべきである。したがって、具体的な厚みや寸法は以下の説明を参酌して判断すべきものである。また、図面相互間においても互いの寸法の関係や比率が異なる部分が含まれていることはもちろんである。なお、以下の説明では、「重量部」を「部」ということがある。
また、以下に示す実施形態は、本発明の技術的思想を具体化するための構成を例示するものであって、本発明の技術的思想は、構成部品の材質、形状、構造等を下記のものに特定するものでない。本発明の技術的思想は、特許請求の範囲に記載された請求項が規定する技術的範囲内において、種々の変更を加えることができる。
Next, an embodiment of the present invention will be described with reference to the drawings.
Here, in the following description of the drawings, the same or similar parts are denoted by the same or similar reference numerals. However, it should be noted that the drawings are schematic, and the relationship between the thickness and the planar dimensions, the ratio of the thickness of each layer, and the like may differ from the actual ones. Therefore, specific thicknesses and dimensions should be determined in consideration of the following description. Moreover, it is a matter of course that portions having different dimensional relationships and ratios are included between the drawings. In the following description, “parts by weight” may be referred to as “parts”.
Further, the embodiment described below exemplifies a configuration for embodying the technical idea of the present invention, and the technical idea of the present invention describes the material, shape, structure, etc. of the component as follows. It is not something specific. The technical idea of the present invention can be variously modified within the technical scope defined by the claims described in the claims.
(構成)
本実施形態の蓄光紙(以下、蓄光シートということがある)は、パルプ材に繊維、蓄光性顔料、及び紙力増強剤を含有してなる。
ここで、本実施形態の蓄光紙に含まれる蓄光性顔料の粒径は、20μm以上50μm以下であり、この蓄光性顔料は、上記パルプ材に対し35重量%以上55重量%以下含まれている。本発明における蓄光性顔料の粒径は、レーザー回折・散乱法によって定義される平均粒径である。例えば、Malvern Instruments Ltd製 レーザー回折式粒度分布測定装置(型番:マスターサイザー3000)を用いてJIS Z8825によりMie理論に基づいた条件で蓄光性顔料の粒径を測定した際に示される値である。
(Constitution)
The phosphorescent paper of the present embodiment (hereinafter sometimes referred to as a phosphorescent sheet) contains a fiber, a phosphorescent pigment, and a paper strength enhancer in a pulp material.
Here, the particle diameter of the phosphorescent pigment contained in the phosphorescent paper of the present embodiment is 20 μm or more and 50 μm or less, and this phosphorescent pigment is contained in an amount of 35 wt% or more and 55 wt% or less with respect to the pulp material. . The particle diameter of the luminous pigment in the present invention is an average particle diameter defined by a laser diffraction / scattering method. For example, the value is shown when the particle diameter of the luminous pigment is measured under the conditions based on the Mie theory according to JIS Z8825 using a laser diffraction particle size distribution measuring device (model number: Mastersizer 3000) manufactured by Malvern Instruments Ltd.
抄紙段階のスラリーに蓄光性顔料を添加することにより、蓄光性のある抄紙を提供することが可能となる。そして、粒径20μm以上50μm以下の蓄光性顔料を、35重量%以上55重量%以下添加することにより、さらに蓄光性の高く、生産性の高い蓄光紙を提供することが可能となる。
また、上記パルプ材は、さらしパルプ又は未さらしパルプのいずれか又は両方を含むことが好ましく、特に、さらしパルプを含むことが好ましい。製紙パルプにさらしパルプを添加することにより、さらに視認性に優れた蓄光性効果の高い蓄光紙を提供することが可能となる。
また、上記繊維は、ガラス繊維又は合成繊維のいずれか又は両方を含むことが好ましい。繊維を添加することにより、さらに強度の高い蓄光紙を提供することが可能となる。
また、本実施形態の蓄光紙の片面、又は両面には、合成樹脂がコーティングされていることが好ましい。
By adding a phosphorescent pigment to the papermaking stage slurry, it is possible to provide a phosphorescent papermaking. Further, by adding a phosphorescent pigment having a particle size of 20 μm or more and 50 μm or less to 35 wt% or more and 55 wt% or less, it is possible to provide a phosphorescent paper having higher phosphorescence and higher productivity.
Moreover, it is preferable that the said pulp material contains either or both of an exposed pulp and an unexposed pulp, and it is especially preferable that an exposed pulp is included. By adding the exposed pulp to the papermaking pulp, it is possible to provide a phosphorescent paper having a further excellent visibility and a high luminous effect.
Moreover, it is preferable that the said fiber contains either or both of glass fiber or synthetic fiber. By adding fibers, it is possible to provide a phosphorescent paper with higher strength.
Moreover, it is preferable that the synthetic resin is coated on one side or both sides of the phosphorescent paper of this embodiment.
<蓄光性顔料>
本実施形態の蓄光紙に含まれる蓄光性顔料は、金属酸化物に希土類元素をドープさせてなる蓄光性顔料であることが好ましい。なお、上記金属酸化物は、アルミン酸ストロンチウムであり、上記希土類元素がランタノイド系希土類元素であることがより好ましい。希土類酸化物をドープさせた蓄光性顔料を添加することにより、さらに蓄光性の高い蓄光紙を提供することが可能となる。
<Luminescent pigment>
The luminous pigment contained in the luminous paper of this embodiment is preferably a luminous pigment formed by doping a rare earth element into a metal oxide. The metal oxide is strontium aluminate, and the rare earth element is more preferably a lanthanoid rare earth element. By adding a phosphorescent pigment doped with a rare earth oxide, it is possible to provide a phosphorescent paper having a higher phosphorescent property.
<蓄光紙の製造方法>
本実施形態の蓄光紙の製造方法は、上記構成を満たす蓄光紙を製造する方法であれば、特に限定されない。
本実施形態の蓄光紙の製造方法は、蓄光性顔料を製造する工程と、この蓄光性顔料、パルプ材、繊維、紙力増強剤、及び水を含んでスラリーを精製(調製)する工程と、上記スラリーを抄紙する工程とを備える。
このとき、上記蓄光性顔料を製造する工程においては、その粒径が20μm以上50μm以下になるように調製される。また、上記スラリーを精製する工程においては、上記蓄光性顔料が上記スラリーに35重量%以上55重量%以下含まれるように調製される。
<Method of manufacturing phosphorescent paper>
The manufacturing method of the phosphorescent paper of this embodiment will not be specifically limited if it is a method of manufacturing the phosphorescent paper which satisfy | fills the said structure.
The method for producing phosphorescent paper of the present embodiment includes a step of producing a phosphorescent pigment, a step of purifying (preparing) a slurry containing the phosphorescent pigment, pulp material, fiber, paper strength enhancer, and water, And paper making the slurry.
At this time, in the step of producing the luminous pigment, the particle size is adjusted to 20 μm or more and 50 μm or less. In the step of refining the slurry, the luminous pigment is prepared so as to be contained in the slurry in an amount of 35% by weight to 55% by weight.
具体的には、例えば、粒径20μm以上50μm以下の蓄光性顔料を、35重量%以上55重量%以下の配合率で、補強材としてのガラス繊維、パルプ等と共に水中に分散させ、坪量200g/m2となるよう手抄きによりすくい取った湿紙を熱ドラムに接触・乾燥させて蓄光紙を作製する。
なお、上述のように手抄きによりすくい取った湿紙を熱ドラムに接触・乾燥させた後、アクリル樹脂(例えば、固形分量が片面23g/m2、合計46g/m2)をコーティングしてもよい。このようにすることで、インクジェット印刷等により絵付けが可能である。
Specifically, for example, a luminous pigment having a particle size of 20 μm or more and 50 μm or less is dispersed in water together with glass fiber, pulp, or the like as a reinforcing material at a blending ratio of 35 wt% or more and 55 wt% or less. The wet paper scooped up by hand-drawing so as to be / m 2 is brought into contact with a thermal drum and dried to produce phosphorescent paper.
In addition, after wet paper scooped by hand-sheeting as described above is contacted and dried on a thermal drum, an acrylic resin (for example, solid content is 23 g / m 2 on one side, total 46 g / m 2 ) is coated. Also good. By doing so, it is possible to paint by inkjet printing or the like.
[蓄光性顔料の製造方法]
ここで、蓄光性顔料を製造する工程について具体的に説明する。
蓄光性顔料は、以下の第1工程〜第3工程を少なくとも経て作製される。
[Method of producing phosphorescent pigment]
Here, the process of manufacturing a luminous pigment is demonstrated concretely.
The phosphorescent pigment is produced through at least the following first to third steps.
−第1工程−
第1工程は、アルカリ土類金属酸化物に希土類元素をドープさせてなる蓄光性顔料の原料粉末を準備する工程である。アルカリ土類金属酸化物としては、上述したように、アルミン酸ストロンチウム化合物、特にSrAl2O4やSr4Al14O25が好ましく、希土類元素としてはランタノイド系希土類元素が好ましく、希土類元素は酸化物の形態にて原料粉末に添加され、特にEu2O3、Dy2O3が好ましいが、これに限定されるものではない。
蓄光性顔料の原料粉末は、市販のアルミン酸塩系蓄光性顔料(蓄光性蛍光体)であっても、以下に例示する製造工程によって製造されたアルミン酸系ストロンチウム蓄光性顔料であってもよく、蓄光性顔料の原料粉末を製造する際の工程としては、以下の工程が挙げられるが、これに限定されるものではない。
-First step-
The first step is a step of preparing a raw material powder of a luminous pigment obtained by doping a rare earth element into an alkaline earth metal oxide. As described above, the alkaline earth metal oxide is preferably a strontium aluminate compound, particularly SrAl 2 O 4 or Sr 4 Al 14 O 25 , and the rare earth element is preferably a lanthanoid rare earth element. In particular, Eu 2 O 3 and Dy 2 O 3 are preferable, but are not limited thereto.
The raw material powder of the phosphorescent pigment may be a commercially available aluminate-based phosphorescent pigment (phosphorescent phosphor) or an aluminate-based strontium phosphorescent pigment produced by the production process exemplified below. The steps for producing the phosphorescent pigment raw material powder include the following steps, but are not limited thereto.
上記アルミン酸系ストロンチウム蓄光性顔料を製造する際には、原料粉末として、球形γ‐Al2O3、SrCO3、Eu2O3、Dy2O3及びH3BO3の粉末をそれぞれ準備し、Al/(Sr+Eu+Dy)のモル比率が1.90〜1.99(好ましくは1.97〜1.99)の範囲内で、しかも、H3BO3の配合量が0.5重量%〜2.5重量%(好ましくは2.0重量%〜2.5重量%)の範囲内となるように秤量した後、上記の粉末を混合し、得られた混合物をるつぼの中に入れて、還元雰囲気下にて1350〜1450℃で2〜4時間加熱し、塊状体とした後、得られた塊状物をボールミリング等により粉砕し、得られた粉砕物をスクリーニングして、均一粒度(好ましくは粒径約20μm以上50μm以下)の蓄光性顔料の原料粉末を得る。
上記の工程により得られた蓄光性顔料原料粉末は、蛍光灯を用いて光照射を行った際に、暗所で黄緑色〜青色に発光する。
When producing the aluminate-based strontium phosphorescent pigment, powders of spherical γ-Al 2 O 3 , SrCO 3 , Eu 2 O 3 , Dy 2 O 3 and H 3 BO 3 are prepared as raw material powders, respectively. The molar ratio of Al / (Sr + Eu + Dy) is in the range of 1.90 to 1.99 (preferably 1.97 to 1.99), and the amount of H 3 BO 3 is 0.5 wt% to 2 After weighing to be within the range of 5 wt% (preferably 2.0 wt% to 2.5 wt%), the above powder is mixed, and the resulting mixture is put into a crucible and reduced. After heating at 1350 to 1450 ° C. for 2 to 4 hours under an atmosphere to form a lump, the lump obtained is pulverized by ball milling or the like, and the obtained pulverized product is screened to obtain a uniform particle size (preferably Particle size of about 20 μm to 50 μm) A raw material powder of a luminous pigment is obtained.
The phosphorescent pigment raw material powder obtained by the above process emits yellowish green to blue light in a dark place when irradiated with light using a fluorescent lamp.
−第2工程−
第2工程では、無機酸とリン酸塩を含む水溶液を準備し、当該水溶液に第1工程で得られた蓄光性顔料の原料粉末を加え、撹拌を行う。この際に使用する無機酸は、塩酸、硝酸及び硫酸から選ばれた少なくとも1種であり、リン酸塩は、リン酸二水素ナトリウム、リン酸二水素アンモニウム及びリン酸水素二アンモニウムから選ばれた少なくとも1種であることが好ましい。この第2工程における撹拌時間は、一般的は20〜30℃の室温にて10〜60分であり、30〜50分がより好ましい。
-Second step-
In a 2nd process, the aqueous solution containing an inorganic acid and a phosphate is prepared, the raw material powder of the luminous pigment obtained at the 1st process is added to the said aqueous solution, and stirring is performed. The inorganic acid used in this case is at least one selected from hydrochloric acid, nitric acid and sulfuric acid, and the phosphate was selected from sodium dihydrogen phosphate, ammonium dihydrogen phosphate and diammonium hydrogen phosphate. It is preferable that there is at least one. The stirring time in the second step is generally 10 to 60 minutes at room temperature of 20 to 30 ° C., and more preferably 30 to 50 minutes.
この第2工程において使用される水溶液中には、上記の蓄光性顔料の原料粉末100重量部に対して4〜14重量部、好ましくは6〜11重量部のリン酸二水素ナトリウムが含有されていることが好ましく、当該水溶液中の無機酸の量については、当該水溶液のpHが酸性(好ましくは5.0以下)となる量が好ましい。
このような無機酸とリン酸塩を含む水溶液を用いる第2工程(酸/リン酸塩処理工程)によって、蓄光性顔料の原料粉末の表面が水に対し不溶性又は難溶性となり、蓄光性顔料の耐水性が改善される。又、この第2工程によって、蓄光性顔料の原料粉末の表面が削られ、表面凹凸が少なくなり、平滑な表面となる。
The aqueous solution used in the second step contains 4 to 14 parts by weight, preferably 6 to 11 parts by weight of sodium dihydrogen phosphate with respect to 100 parts by weight of the raw material powder of the luminous pigment. The amount of the inorganic acid in the aqueous solution is preferably such that the pH of the aqueous solution is acidic (preferably 5.0 or less).
By the second step (acid / phosphate treatment step) using such an aqueous solution containing an inorganic acid and a phosphate, the surface of the raw material powder of the phosphorescent pigment becomes insoluble or hardly soluble in water. Water resistance is improved. Moreover, the surface of the raw material powder of the phosphorescent pigment is shaved by this second step, and the surface unevenness is reduced, resulting in a smooth surface.
−第3工程−
更に、第3工程では、第2工程の酸/リン酸塩処理によって得られた蓄光性顔料を水で洗浄するか、あるいは、アルカリ水溶液で中和処理を行った後に水分を除去(脱水)し、乾燥を行い、蓄光性顔料を得る。この際、水での洗浄は、複数回(好ましくは4〜6回)行うことが好ましく、アルカリ水溶液で中和処理を行う場合には、蓄光性顔料を含む水溶液のpHを6.8〜7.2の範囲に調整することが好ましい。本実施形態では、上記アルカリ水溶液の種類は特に限定されないが、水酸化ナトリウム水溶液が一般的である。
この第3工程における乾燥は室温で行っても、加温下(100℃以下)で行っても良い。
上記の第3工程により、蓄光性顔料の表面に付着している不純物が洗い流され、未処理の蓄光性顔料(第1工程で準備した未処理の蓄光性顔料の原料粉末)に比べて、高い初期残光輝度特性及び耐水性を備えた蓄光性顔料が得られる。
-Third step-
Further, in the third step, the phosphorescent pigment obtained by the acid / phosphate treatment in the second step is washed with water or neutralized with an alkaline aqueous solution and then water is removed (dehydrated). And drying to obtain a luminous pigment. At this time, the washing with water is preferably performed a plurality of times (preferably 4 to 6 times). When neutralization is performed with an alkaline aqueous solution, the pH of the aqueous solution containing the luminous pigment is 6.8 to 7 It is preferable to adjust to the range of. In the present embodiment, the type of the alkaline aqueous solution is not particularly limited, but a sodium hydroxide aqueous solution is common.
The drying in the third step may be performed at room temperature or under heating (100 ° C. or less).
By the third step, impurities adhering to the surface of the luminous pigment are washed away, which is higher than the untreated luminous pigment (raw powder of raw phosphorescent pigment prepared in the first step). A phosphorescent pigment having initial afterglow luminance characteristics and water resistance is obtained.
(他の実施形態)
他の実施形態として、上記のアルカリ処理を行う代わりに、第2工程で得られた蓄光性顔料を溶液から取り出して水で5回洗浄し、蓄光性顔料の表面に付着している不純物を洗い流した後、脱水・乾燥を行い、pH調整なしの酸/リン酸塩処理グリーン系の蓄光性顔料を得てもよい。
(Other embodiments)
As another embodiment, instead of performing the alkali treatment, the phosphorescent pigment obtained in the second step is taken out of the solution and washed five times with water to wash away impurities adhering to the surface of the phosphorescent pigment. Then, dehydration and drying may be performed to obtain an acid / phosphate treated green phosphorescent pigment without pH adjustment.
また、その他の実施形態として、第1工程を次のようにしてもよい。すなわち、市販の球形γ‐Al2O3 2650g(25.99モル)と、高純度SrCO3 2115g(14.33モル)と、Eu2O3 55g(0.16モル)と、Dy2O3 38g(0.10モル)と、H3BO3 142g(2.30モル)を秤量し、これらを湿式方法にて混合することにより固体混合物5kgを得る。そして、この固体混合物をるつぼに入れ、還元雰囲気下にて1400℃で3時間反応させて塊状体を得、冷却を行った後、この塊状体をボールミルにて粉砕し、スクリーニング(篩分け)を行うことによって、均一な粒度(粒子径約20μm以上50μm以下)を有する未処理の蓄光性顔料の粉末(化学式:Sr4Al14O25)を生成させる。その後、上記の第2工程、第3工程を経て、pH調整ありの酸/リン酸塩処理ブルー系蓄光性顔料と、pH調整なしの酸/リン酸塩処理ブルー系蓄光性顔料を得ることができる。 Further, as another embodiment, the first step may be performed as follows. That is, a commercially available spherical γ-Al 2 O 3 2650g ( 25.99 moles), and high purity SrCO 3 2115g (14.33 moles), and Eu 2 O 3 55g (0.16 mol), Dy 2 O 3 38 g (0.10 mol) and 142 g (2.30 mol) of H 3 BO 3 are weighed and mixed by a wet method to obtain 5 kg of a solid mixture. Then, this solid mixture is put in a crucible and reacted at 1400 ° C. for 3 hours in a reducing atmosphere to obtain a lump. After cooling, this lump is crushed with a ball mill, and screening (sieving) is performed. By carrying out, an untreated phosphorescent pigment powder (chemical formula: Sr 4 Al 14 O 25 ) having a uniform particle size (particle diameter of about 20 μm to 50 μm) is generated. Thereafter, an acid / phosphate-treated blue phosphorescent pigment with pH adjustment and an acid / phosphate-treated blue phosphorescent pigment without pH adjustment can be obtained through the second and third steps. it can.
以下、実施例及び比較例を示して本発明を具体的に説明する。ただし、本発明は以下の実施例に限定されるものではない。
(実施例1)
<蓄光紙の作製>
[蓄光性顔料の作製]
第1工程:市販の球形γ‐Al2O3 1975g(19.36モル)と、高純度SrCO3 2793g(18.92モル)と、Eu2O3 49g(0.14モル)と、Dy2O3 60g(0.16モル)と、H3BO3 123g(2.00モル)を秤量し、これらを湿式方法にて混合することにより固体混合物5kgを得た。そして、この固体混合物をるつぼに入れ、還元雰囲気下にて1400℃で3時間反応させて塊状体を得、冷却を行った後、この塊状体をボールミルにて粉砕し、スクリーニング(篩分け)を行うことによって、均一な粒度(粒子径約30μm)を有する未処理の蓄光性顔料の粉末(化学式:SrAl2O4)を生成させた。この粉末に白色のLEDランプを用いて光照射したところ、暗所において黄緑色(イエローグリーン)に発光することが確認された。
Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples. However, the present invention is not limited to the following examples.
Example 1
<Production of phosphorescent paper>
[Production of phosphorescent pigment]
First step: the commercial spherical γ-Al 2 O 3 1975g ( 19.36 moles), and high purity SrCO 3 2793g (18.92 moles), and Eu 2 O 3 49g (0.14 mol), Dy 2 60 g (0.16 mol) of O 3 and 123 g (2.00 mol) of H 3 BO 3 were weighed and mixed by a wet method to obtain 5 kg of a solid mixture. Then, this solid mixture is put in a crucible and reacted at 1400 ° C. for 3 hours in a reducing atmosphere to obtain a lump. After cooling, this lump is crushed with a ball mill, and screening (sieving) is performed. By carrying out, an untreated phosphorescent pigment powder (chemical formula: SrAl 2 O 4 ) having a uniform particle size (particle diameter of about 30 μm) was produced. When this powder was irradiated with light using a white LED lamp, it was confirmed that the powder emitted yellow-green light in a dark place.
第2工程:50mlの水をビーカーに入れ、この中にリン酸塩としてNaH2PO4・2H2O 6.3g(0.04モル)を添加し(pH4.8)、更にHNO3水溶液(12.9N)3.2mlを添加し、酸/リン酸塩処理溶液(pH1.2)を調製した。この処理溶液に、第1工程で製造した蓄光性顔料原料粉末62.5gを加え、40分間攪拌を行った。この時の処理溶液のpHは2.5であった。
第3工程:アルカリ水溶液として、NaOH水溶液(0.25N)を準備し、第2工程で得られた蓄光性顔料を含む溶液に、このアルカリ水溶液60mlを加えて、溶液のpHが7.0になるように調整し、脱水した後、乾燥を行い、pH調整ありの酸/リン酸塩処理グリーン系の蓄光性顔料を得た。
以上のようにして作製された粒径30μmの蓄光性顔料を配合率50%、補強材としてのガラス繊維、パルプ等を水中に分散させ、坪量200g/m2となるよう手抄きによりすくい取った湿紙を熱ドラムに接触・乾燥させ、実施例1の蓄光紙を作製した。
Second step: 50 ml of water was put into a beaker, and 6.3 g (0.04 mol) of NaH 2 PO 4 .2H 2 O as a phosphate was added thereto (pH 4.8), and an aqueous HNO 3 solution ( 12.9N) 3.2 ml was added to prepare an acid / phosphate treatment solution (pH 1.2). To this treatment solution, 62.5 g of the luminous pigment raw material powder produced in the first step was added and stirred for 40 minutes. The pH of the treatment solution at this time was 2.5.
Third step: An aqueous NaOH solution (0.25N) is prepared as an alkaline aqueous solution, and 60 ml of this alkaline aqueous solution is added to the solution containing the luminous pigment obtained in the second step, so that the pH of the solution becomes 7.0. Then, after dehydrating, drying was performed to obtain an acid / phosphate-treated green phosphorescent pigment with pH adjustment.
The phosphorescent pigment having a particle size of 30 μm prepared as described above is mixed in 50%, glass fiber, pulp, etc. as a reinforcing material is dispersed in water and scooped by hand-drawing so that the basis weight becomes 200 g / m 2. The wet paper taken was contacted with a thermal drum and dried to produce the phosphorescent paper of Example 1.
<評価>
作製した実施例1の蓄光紙について、以下の要領で「輝度」及び「生産性」を評価した。
[輝度]
実施例1の蓄光紙の(燐光)輝度の測定については、JIS Z9107(2008)の副分類JAに準拠した方法で測定を行った。
輝度の測定用の試験片として、70×150mmにサンプルを切り出した後、20℃、65%RH環境に試験片を24時間放置した。
その後、20℃65%RH環境にて、輝度計(コニカミノルタオプティクス株式会社製、LS‐100)を用いて、標準光D65を200ルクスに20分照射した後、光源を遮断し、20分後及び60分後の輝度を測定した。
評価基準として、20分後の輝度が24mcd/m2以上を〇、20分後の輝度が24mcd/m2以上かつ60分後の輝度が7mcd/m2以上を◎、その他(20分後の輝度が24mcd/m2未満)を×として評価した。評価結果を表1に示す。
<Evaluation>
About the produced phosphorescent paper of Example 1, "luminance" and "productivity" were evaluated in the following ways.
[Luminance]
About the measurement of the (phosphorescence) brightness | luminance of the phosphorescent paper of Example 1, it measured by the method based on subclass JA of JISZ9107 (2008).
As a test piece for measuring luminance, a sample was cut out to 70 × 150 mm, and then left in a 20 ° C., 65% RH environment for 24 hours.
After that, using a luminance meter (LS-100, manufactured by Konica Minolta Optics, Inc.) at 20 ° C. and 65% RH, the standard light D65 was irradiated to 200 lux for 20 minutes, the light source was cut off, and after 20 minutes And the brightness | luminance after 60 minutes was measured.
As evaluation criteria, the luminance after 20 minutes is ◯ when the luminance is 24 mcd / m 2 or more, the luminance after 20 minutes is 24 mcd / m 2 or more and the luminance after 60 minutes is 7 mcd / m 2 or more, and other (after 20 minutes The luminance was evaluated as x when less than 24 mcd / m 2 . The evaluation results are shown in Table 1.
[生産性(顔料歩留まり)]
実施例1の蓄光紙に対して、抄紙時の脱水廃液の吸光度を測定し、予め作成しておいた検量線から濃度に換算して、100−(脱水廃液の顔料濃度/添加した顔料濃度)×100により顔料歩留まりを算出した。この顔料歩留まりが80%以上を生産性:○とし、顔料歩留まりが80%未満を生産性:×として評価した。評価結果を表1に示す。
[Productivity (pigment yield)]
For the phosphorescent paper of Example 1, the absorbance of the dehydrated waste liquid at the time of paper making was measured, and converted to a concentration from a calibration curve prepared in advance, 100- (pigment concentration of dehydrated waste liquid / added pigment concentration) The pigment yield was calculated from x100. The pigment yield was evaluated as 80% or more as productivity: ◯, and the pigment yield as less than 80% as productivity: x. The evaluation results are shown in Table 1.
(実施例2)
実施例1における補強材として、ガラス繊維に替えてポリエステルを混抄させた以外は実施例1と同じ方法で実施例2の蓄光紙を作製した。その後、実施例2の蓄光紙の輝度、及び生産性について実施例1と同様に評価した。実施例1と同様に、実施例2の蓄光紙の詳細と評価結果とを表1に示す。
(実施例3)
坪量を150g/m2とした以外は実施例1と同じ方法で実施例3の蓄光紙を作製した。その後、実施例3の蓄光紙の輝度、及び生産性について実施例1と同様に評価した。実施例1と同様に、実施例3の蓄光紙の詳細と評価結果とを表1に示す。
(Example 2)
As a reinforcing material in Example 1, phosphorescent paper of Example 2 was produced in the same manner as in Example 1 except that polyester was mixed instead of glass fiber. Thereafter, the luminance and productivity of the phosphorescent paper of Example 2 were evaluated in the same manner as in Example 1. Similar to Example 1, the details and evaluation results of the phosphorescent paper of Example 2 are shown in Table 1.
(Example 3)
A phosphorescent paper of Example 3 was produced in the same manner as in Example 1 except that the basis weight was 150 g / m 2 . Thereafter, the brightness and productivity of the phosphorescent paper of Example 3 were evaluated in the same manner as in Example 1. As in Example 1, the details and evaluation results of the phosphorescent paper of Example 3 are shown in Table 1.
(比較例1)
粒径13μmの蓄光性顔料を使用した以外は実施例1と同じ方法で比較例1の蓄光紙を作製した。その後、比較例1の蓄光紙の輝度、及び生産性について実施例1と同様に評価した。実施例1と同様に、比較例1の蓄光紙の詳細と評価結果とを表1に示す。
(比較例2)
粒径13μmの蓄光性顔料を使用した以外は実施例2と同じ方法で比較例2の蓄光紙を作製した。その後、比較例2の蓄光紙の輝度、及び生産性について実施例1と同様に評価した。実施例1と同様に、比較例2の蓄光紙の詳細と評価結果とを表1に示す。
(Comparative Example 1)
A phosphorescent paper of Comparative Example 1 was prepared in the same manner as in Example 1 except that a phosphorescent pigment having a particle size of 13 μm was used. Thereafter, the luminance and productivity of the phosphorescent paper of Comparative Example 1 were evaluated in the same manner as in Example 1. Similar to Example 1, the details and evaluation results of the phosphorescent paper of Comparative Example 1 are shown in Table 1.
(Comparative Example 2)
A phosphorescent paper of Comparative Example 2 was produced in the same manner as in Example 2 except that a phosphorescent pigment having a particle size of 13 μm was used. Thereafter, the brightness and productivity of the phosphorescent paper of Comparative Example 2 were evaluated in the same manner as in Example 1. As in Example 1, the details and evaluation results of the phosphorescent paper of Comparative Example 2 are shown in Table 1.
(比較例3)
原料に粒径60μmの蓄光性顔料を配合率70%、坪量150g/m2とした以外は実施例1と同じ方法で比較例3の蓄光紙を作製した。その後、比較例3の蓄光紙の輝度、及び生産性について実施例1と同様に評価した。実施例1と同様に、比較例3の蓄光紙の詳細と評価結果とを表1に示す。
(比較例4)
原料に粒径30μmの蓄光性顔料を使用した以外は比較例3と同じ方法で比較例4の蓄光紙を作製した。その後、比較例4の蓄光紙の輝度、及び生産性について実施例1と同様に評価した。実施例1と同様に、比較例4の蓄光紙の詳細と評価結果とを表1に示す。
(Comparative Example 3)
A phosphorescent paper of Comparative Example 3 was prepared in the same manner as in Example 1 except that a phosphorescent pigment having a particle size of 60 μm was used as the raw material and the blending ratio was 70% and the basis weight was 150 g / m 2 . Thereafter, the brightness and productivity of the phosphorescent paper of Comparative Example 3 were evaluated in the same manner as in Example 1. Similar to Example 1, the details and evaluation results of the phosphorescent paper of Comparative Example 3 are shown in Table 1.
(Comparative Example 4)
A phosphorescent paper of Comparative Example 4 was produced in the same manner as Comparative Example 3 except that a phosphorescent pigment having a particle size of 30 μm was used as a raw material. Thereafter, the luminance and productivity of the phosphorescent paper of Comparative Example 4 were evaluated in the same manner as in Example 1. Similar to Example 1, the details and evaluation results of the phosphorescent paper of Comparative Example 4 are shown in Table 1.
<評価結果>
表1から分かるように、実施例1,2の蓄光紙は、ともに輝度が特に高く、蓄光性顔料の歩留が高いため生産性に優れていた。また、実施例3の蓄光紙は、輝度が高く、蓄光性顔料の歩留が高いため生産性に優れていた。
これらに対して、比較例1,2の蓄光紙は、蓄光性顔料の歩留が高く生産性に優れるが、輝度が低かった。また、比較例3の蓄光紙は、輝度は高いが、蓄光性顔料の歩留が低く、生産性に劣っていた。また、比較例4の蓄光紙は、輝度も低く、さらに蓄光性顔料歩の留も低く生産性に劣っていた。
すなわち、本発明の範囲である実施例1〜3の蓄光紙では、生産性が高く、蓄光性(輝度)が高いことが分かる。
<Evaluation results>
As can be seen from Table 1, the phosphorescent papers of Examples 1 and 2 were both excellent in productivity because of their particularly high luminance and high yield of the phosphorescent pigment. Further, the phosphorescent paper of Example 3 was excellent in productivity because of high brightness and a high yield of phosphorescent pigment.
On the other hand, the phosphorescent papers of Comparative Examples 1 and 2 had high yield of phosphorescent pigments and excellent productivity, but low brightness. Moreover, although the luminous paper of the comparative example 3 had high brightness | luminance, the yield of the luminous pigment was low and it was inferior to productivity. Further, the phosphorescent paper of Comparative Example 4 had a low brightness, a low yield of phosphorescent pigment, and a poor productivity.
That is, it can be seen that the phosphorescent papers of Examples 1 to 3, which are the scope of the present invention, have high productivity and high phosphorescence (luminance).
Claims (12)
前記蓄光性顔料の粒径が20μm以上50μm以下であり、前記蓄光性顔料が前記パルプ材に対し35重量%以上55重量%以下含まれたことを特徴とする蓄光紙。 Contains pulp, fiber, luminous pigment, and paper strength enhancer,
A phosphorescent paper, wherein a particle diameter of the phosphorescent pigment is 20 μm or more and 50 μm or less, and the phosphorescent pigment is contained in an amount of 35 wt% or more and 55 wt% or less with respect to the pulp material.
前記スラリーを抄紙して蓄光紙を作製する蓄光紙の製造方法であって、
前記蓄光性顔料の粒径が20μm以上50μm以下であり、前記蓄光性顔料が前記スラリーに35重量%以上55重量%以下含まれていることを特徴とする蓄光紙の製造方法。 Refining the slurry containing phosphorescent pigment, pulp material, fiber, paper strength enhancer, and water;
A method for producing phosphorescent paper that produces the phosphorescent paper by making paper from the slurry,
The phosphorescent pigment has a particle size of 20 μm or more and 50 μm or less, and the slurry contains 35 wt% or more and 55 wt% or less of the phosphorescent pigment.
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WO2002101146A1 (en) * | 2001-05-11 | 2002-12-19 | Arina Nakayama | Luminous paper and production method thereof and utilization method thereof |
JP2007284822A (en) * | 2006-04-17 | 2007-11-01 | Oji Paper Co Ltd | Porous filler and method for producing the same, and porous filler slurry and paper |
JP2012187869A (en) * | 2011-03-11 | 2012-10-04 | Kj Specialty Paper Co Ltd | Phosphorescent decorative laminate |
JP2016098454A (en) * | 2014-11-21 | 2016-05-30 | 大日本印刷株式会社 | Form sheet |
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JPH04119183A (en) * | 1990-09-04 | 1992-04-20 | Mitsubishi Paper Mills Ltd | Light-accumulating luminescent nonwoven fabric and its production |
WO2002101146A1 (en) * | 2001-05-11 | 2002-12-19 | Arina Nakayama | Luminous paper and production method thereof and utilization method thereof |
JP2007284822A (en) * | 2006-04-17 | 2007-11-01 | Oji Paper Co Ltd | Porous filler and method for producing the same, and porous filler slurry and paper |
JP2012187869A (en) * | 2011-03-11 | 2012-10-04 | Kj Specialty Paper Co Ltd | Phosphorescent decorative laminate |
JP2016098454A (en) * | 2014-11-21 | 2016-05-30 | 大日本印刷株式会社 | Form sheet |
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