JP2006022215A - Time-erasable ink composition - Google Patents
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- 239000000203 mixture Substances 0.000 title claims abstract description 47
- 239000000976 ink Substances 0.000 title claims description 70
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 14
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 14
- 239000011347 resin Substances 0.000 claims abstract description 13
- 229920005989 resin Polymers 0.000 claims abstract description 13
- 239000003960 organic solvent Substances 0.000 claims abstract description 10
- -1 polyoxyethylene Polymers 0.000 claims description 27
- 239000004094 surface-active agent Substances 0.000 claims description 15
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- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 claims description 4
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- 150000003839 salts Chemical class 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 235000011187 glycerol Nutrition 0.000 claims description 3
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- 229920001214 Polysorbate 60 Polymers 0.000 claims description 2
- 150000003973 alkyl amines Chemical class 0.000 claims description 2
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 150000005215 alkyl ethers Chemical class 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- 150000004693 imidazolium salts Chemical class 0.000 claims description 2
- 239000000123 paper Substances 0.000 abstract description 8
- 239000002023 wood Substances 0.000 abstract description 6
- 239000011248 coating agent Substances 0.000 abstract description 5
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- 239000002184 metal Substances 0.000 abstract description 5
- 229910052751 metal Inorganic materials 0.000 abstract description 5
- 230000002745 absorbent Effects 0.000 abstract description 4
- 239000002250 absorbent Substances 0.000 abstract description 4
- 239000003086 colorant Substances 0.000 abstract description 2
- 239000011505 plaster Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000000975 dye Substances 0.000 description 14
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000010440 gypsum Substances 0.000 description 4
- 229910052602 gypsum Inorganic materials 0.000 description 4
- 241000218645 Cedrus Species 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 238000004042 decolorization Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 125000001174 sulfone group Chemical group 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- RHLPAVIBWYPLRV-UHFFFAOYSA-N 2-hydroxy-4-sulfobenzoic acid Chemical compound OC(=O)C1=CC=C(S(O)(=O)=O)C=C1O RHLPAVIBWYPLRV-UHFFFAOYSA-N 0.000 description 1
- UYMBCDOGDVGEFA-UHFFFAOYSA-N 3-(1h-indol-2-yl)-3h-2-benzofuran-1-one Chemical class C12=CC=CC=C2C(=O)OC1C1=CC2=CC=CC=C2N1 UYMBCDOGDVGEFA-UHFFFAOYSA-N 0.000 description 1
- MTMKZABGIQJAEX-UHFFFAOYSA-N 4,4'-sulfonylbis[2-(prop-2-en-1-yl)phenol] Chemical compound C1=C(CC=C)C(O)=CC=C1S(=O)(=O)C1=CC=C(O)C(CC=C)=C1 MTMKZABGIQJAEX-UHFFFAOYSA-N 0.000 description 1
- ZTILAOCGFRDHBH-UHFFFAOYSA-N 4-(4-propan-2-yloxyphenyl)sulfonylphenol Chemical compound C1=CC(OC(C)C)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 ZTILAOCGFRDHBH-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical class F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000008378 aryl ethers Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- MFGZXPGKKJMZIY-UHFFFAOYSA-N ethyl 5-amino-1-(4-sulfamoylphenyl)pyrazole-4-carboxylate Chemical compound NC1=C(C(=O)OCC)C=NN1C1=CC=C(S(N)(=O)=O)C=C1 MFGZXPGKKJMZIY-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 125000005489 p-toluenesulfonic acid group Chemical group 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000004961 triphenylmethanes Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Abstract
Description
本発明は、木材、紙、石膏ボードなどの吸収面や金属、ガラスなど非吸収面に筆記又は塗布し、筆跡が鮮明に発色し、自然に発色状態から無色に変化する経時消去性インキ組成物に関する。特に、墨壷用墨汁等の墨壷用インキとして好適に用いることができる経時消去性インキ組成物に関する。 The present invention is a time-erasable ink composition in which writing or coating is performed on an absorbing surface such as wood, paper, or gypsum board, or a non-absorbing surface such as metal or glass, and the handwriting is clearly colored and naturally changes from a colored state to colorless. About. In particular, the present invention relates to an erasable ink composition that can be suitably used as ink for ink brushes such as ink for ink.
従来、ロイコ染料及び顕色剤を用いて、水により筆跡を消去することができる水消去性インキ組成物が種々提供されている（特許文献１〜特許文献１５）。すなわち、ロイコ染料を顕色剤で着色し、これを含むインキを用いて筆記乃至塗布した後、その筆跡に水を付着させることにより、顕色剤が水に溶解し、水に溶けない染料から顕色剤が離脱し、ロイコ染料が元の無色の構造に戻ることにより消去するインキ組成物である。 Conventionally, various water-erasable ink compositions that can erase handwriting with water using a leuco dye and a developer have been provided (Patent Documents 1 to 15). That is, after coloring or coating leuco dye with a developer and writing or coating using ink containing the leuco dye, the developer is dissolved in water by attaching water to the handwriting, and from a dye that does not dissolve in water The ink composition is erased when the developer is released and the leuco dye returns to its original colorless structure.
しかし、従来のこれらの消去性インキ組成物では、筆記後に水によって消去するインキであり、筆記後自然に発色状態から無色に変化する経時消去性インキ組成物は未だ提供されていない。ここでいう経時消去性とは、時間と共に無色に変化することを示している。 However, these conventional erasable ink compositions are inks that are erased with water after writing, and a time-erasable ink composition that spontaneously changes from a colored state to colorless after writing has not yet been provided. Here, the erasability with time indicates that the color changes with time.
本発明の課題は、木材、紙、石膏ボードなどの吸収面や金属、ガラスなど非吸収面に筆記又は塗布すると、筆跡が鮮明に発色するが、その後経時的に自然に発色状態から無色に変化する経時消去性インキ組成物を提供するところにある。 The problem with the present invention is that when writing or applying to an absorbing surface such as wood, paper, or gypsum board, or a non-absorbing surface such as metal or glass, the handwriting clearly develops color, but then gradually changes from a colored state to colorless over time. The present invention provides a time-erasable ink composition.
上記課題を解決するため鋭意検討した結果、ロイコ染料、顕色剤、ノニオン系又はカチオン系界面活性剤及び有機溶剤を含むインキ組成物であれば、筆記後自然に発色状態から無色に変化することを見出し、本発明を完成した。
本請求項１の発明は、ロイコ染料、顕色剤、ノニオン系又はカチオン系界面活性剤及び有機溶剤を含む経時消去性インキ組成物である。
As a result of intensive studies to solve the above problems, an ink composition containing a leuco dye, a developer, a nonionic or cationic surfactant, and an organic solvent will naturally change from a colored state to colorless after writing. The present invention has been completed.
The invention of claim 1 is a time-erasable ink composition comprising a leuco dye, a developer, a nonionic or cationic surfactant and an organic solvent.
なお、ロイコ染料及び顕色剤に対し、アニオン系界面活性剤は経時消去性がなく、経時消去性はノニオン系又はカチオン系界面活性剤に特異的にみられる現象である。ノニオン系又はカチオン系界面活性剤は、インキ組成物全量に対して０．２〜２０重量％、好ましくは０．５〜１０重量％、より好ましくは顕色剤０．２〜２０重量％に対して０．２〜２０重量％、さらに好適には０．５〜１０重量％含ませることが好ましい。上記界面活性剤を０．２〜２０重量％、好ましくは０．５〜１０重量％の量的範囲内で含有量を調節することにより、経時消去性の速度を制御することができ、界面活性剤の含有量を多くすることにより経時消去性の速度を早くすることができ、界面活性剤の含有量を少なくすることにより経時消去性の速度を遅延させることができる。上記界面活性剤が０．２重量％未満では消去し難く、２０重量％を超えると発色濃度が薄くなる。 In contrast to leuco dyes and developers, anionic surfactants do not have erasability over time, and erasability over time is a phenomenon that is specifically observed in nonionic or cationic surfactants. The nonionic or cationic surfactant is 0.2 to 20% by weight, preferably 0.5 to 10% by weight, more preferably 0.2 to 20% by weight, based on the total amount of the ink composition. 0.2 to 20% by weight, more preferably 0.5 to 10% by weight. By adjusting the content of the surfactant in a quantitative range of 0.2 to 20% by weight, preferably 0.5 to 10% by weight, the erasability with time can be controlled, and the surface activity Increasing the content of the agent can increase the erasability with time, and decreasing the surfactant content can delay the erasability with time. If the surfactant is less than 0.2% by weight, it is difficult to erase, and if it exceeds 20% by weight, the color density is reduced.
なお、初期発色濃度を大きくするために、顕色剤としてスルホン系顕色剤、特にｐ−トルエンスルホン酸、スルホサリチル酸及びナフタレンスルホン酸の群から選ばれる１又は２以上の有機酸を用いることが好ましい。 In order to increase the initial color density, it is possible to use a sulfone developer, particularly one or more organic acids selected from the group of p-toluenesulfonic acid, sulfosalicylic acid and naphthalenesulfonic acid, as the developer. preferable.
なお、さらに水溶性樹脂を含有するインキ組成物とすれば、筆記後自然に消去する過程で、強制的に水により消去する機能も兼備することができる。 If the ink composition further contains a water-soluble resin, it can have a function of forcibly erasing with water in the process of erasing naturally after writing.
これにより、木材、紙、石膏ボードなどの吸収面や金属、ガラスなど非吸収面に筆記又は塗布すると、筆跡が鮮明に発色するが、その後経時的に自然に発色状態から無色に変化する経時消去性インキ組成物が得られる。
従って、同インキを墨壷用インキとして適用した場合、これを墨糸乃至墨綿に含ませ、木材等に墨打ちしても、従来の墨汁と異なり、経時的に自然に消去することから、墨打ち後に消去する手間がなくなるもので、従来にない墨壷用墨汁等の墨壷用インキとして好適に用いることができる。なお、墨壷用インキとして、ノニオン系又はカチオン系界面活性剤は、インキ組成物全量に対して好ましくは０．２〜２０重量％、より好ましくは０．５〜１０重量％含ませることが好ましい。
As a result, when writing or applying to non-absorbing surfaces such as wood, paper, gypsum board, and non-absorbing surfaces such as metal and glass, the handwriting will clearly develop color, but then erase over time that naturally changes from colored to colorless over time Ink composition is obtained.
Therefore, when the same ink is applied as ink for ink brush ink, it is included in the ink thread or cotton, and even if it is made on wood or the like, it is erased naturally over time, unlike traditional ink, so It eliminates the hassle of erasing after striking, and can be suitably used as an ink for ink brushes, such as an ink brush for ink that has never been used before. As the ink for ink buds, the nonionic or cationic surfactant is preferably contained in an amount of 0.2 to 20% by weight, more preferably 0.5 to 10% by weight based on the total amount of the ink composition.
本発明で用いられるロイコ染料としては、トリフェニルメタン系、フルオラン系、スビロビラン系、インドリルフタリド系、ローダミンラクタム系、ロイコオーラミン系などを例示することができ、特に限定されるものではない。
上記ロイコ染料は、インキ組成物全量に対して０．１〜５重量％含ませることができ、好ましい含有量は０．５〜３重量％である。上記ロイコ染料がインキ組成物全量に対して５重量％を超えるとインキ組成物に溶解することが困難であり、０．１重量％未満では発色濃度が薄く、筆記直後の筆跡の初期発色性が乏しい。
Examples of the leuco dye used in the present invention include triphenylmethane series, fluorane series, suvirobirane series, indolylphthalide series, rhodamine lactam series, and leucoolamine series, and are not particularly limited. .
The leuco dye can be contained in an amount of 0.1 to 5% by weight with respect to the total amount of the ink composition, and the preferred content is 0.5 to 3% by weight. If the leuco dye exceeds 5% by weight with respect to the total amount of the ink composition, it is difficult to dissolve in the ink composition. If it is less than 0.1% by weight, the color density is low, and the initial color developability of the handwriting immediately after writing is low. poor.
本発明で用いられる顕色剤は、限定されるものではなく、サリチル酸亜鉛、没食子酸、ポリオキシアルキレンモノアリルモノメチルエーテル／無水マレイン酸／スチレン共重合体、ポリオキシエチレンアルキルエーテル化カルボン酸、ポリオキシエチレンアリールエーテル燐酸エステル、ポリオキシエチレンアルキルエーテル燐酸エステル、ｐ−スルホサリチル酸、Ｐ−トルエンスルホン酸、ナフタリンスルホン酸、乳酸、酒石酸、クエン酸などの水溶性顕色剤のほか、非水溶性顕色剤としてビスフェノールＡや、４，４’−ジヒドロキシジフェニルスルホンで示されるビスフェノールＳ、ビス−（３−アリル−４−ヒドロキシフェニル）−スルホン、４−ヒドロキシ−４’−イソプロポキシジフェニルスルホンなどのビスフェノールＳ誘導体を用いることができる。これらは１種又は２種以上を混合して用いることも可能である。 The color developer used in the present invention is not limited. Zinc salicylate, gallic acid, polyoxyalkylene monoallyl monomethyl ether / maleic anhydride / styrene copolymer, polyoxyethylene alkyl etherified carboxylic acid, polyoxyethylene In addition to water-soluble developers such as oxyethylene aryl ether phosphate, polyoxyethylene alkyl ether phosphate, p-sulfosalicylic acid, P-toluenesulfonic acid, naphthalenesulfonic acid, lactic acid, tartaric acid, citric acid, etc. Bisphenol A such as bisphenol A, bisphenol S represented by 4,4′-dihydroxydiphenylsulfone, bis- (3-allyl-4-hydroxyphenyl) -sulfone, 4-hydroxy-4′-isopropoxydiphenylsulfone as a colorant S induction It can be used. These may be used alone or in combination of two or more.
なお、初期発色性の点では、スルホン基を有する有機酸、中でもスルホン基を有する水溶性の有機酸が好ましい。具体的には、ｐ−トルエンスルホン酸、スルホサリチル酸、ナフタレンスルホン酸などが挙げられ、本発明では、前記顕色剤として、ｐ−トルエンスルホン酸、スルホサリチル酸及びナフタレンスルホン酸の群から選ばれる１又は２以上の有機酸を用いることが好ましい。 In terms of initial color developability, an organic acid having a sulfone group, particularly a water-soluble organic acid having a sulfone group is preferable. Specifically, p-toluenesulfonic acid, sulfosalicylic acid, naphthalenesulfonic acid and the like can be mentioned. In the present invention, the developer is selected from the group consisting of p-toluenesulfonic acid, sulfosalicylic acid and naphthalenesulfonic acid. Alternatively, it is preferable to use two or more organic acids.
上記顕色剤は、インキ組成物全量に対して、０．２〜２０重量％含ませることができ、好ましい含有量は０．５〜１０重量％である。上記顕色剤がインキ組成物全量に対して２０重量％を超えると、経時消去性が低下し、０．２重量％未満では発色濃度が薄く、筆記直後の筆跡の初期発色性が乏しい。 The developer can be contained in an amount of 0.2 to 20% by weight with respect to the total amount of the ink composition, and the preferred content is 0.5 to 10% by weight. When the developer exceeds 20% by weight with respect to the total amount of the ink composition, the erasability is deteriorated with time. When the developer is less than 0.2% by weight, the color density is low, and the initial color developability of the handwriting immediately after writing is poor.
上記顕色剤は、インキ組成物全量中、ロイコ染料０．１〜５重量％に対してそれぞれ０．２〜２０重量％含ませることが好ましい。 The developer is preferably contained in an amount of 0.2 to 20% by weight based on 0.1 to 5% by weight of the leuco dye in the total amount of the ink composition.
本発明で用いる界面活性剤は、ノニオン系又はカチオン系界面活性剤である。既述の通り、アニオン系界面活性剤は経時消去性がなく、経時消去性はノニオン系又はカチオン系界面活性剤に特異的にみられる現象である。 The surfactant used in the present invention is a nonionic or cationic surfactant. As described above, anionic surfactants do not have erasability with time, and erasability with time is a phenomenon that is specifically observed in nonionic or cationic surfactants.
本発明で用いるノニオン系界面活性剤としては、ポリオキシエチレンアルキルエーテル、ポリオキシエチレンアルキルアリルエーテル、ポリオキシエチレンアルキルエステル、ソルビタン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ポリオキシエチレンアルキルアミン、アルキルアルカノールアミド、グリセリン脂肪酸エステル及びポリオキシエチレン誘導体を例示することができ、これらの群から選ばれるノニオン系界面活性剤を含むインキ組成物が好ましい。 Nonionic surfactants used in the present invention include polyoxyethylene alkyl ether, polyoxyethylene alkyl allyl ether, polyoxyethylene alkyl ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene alkylamine, alkyl alkanol. Examples thereof include amides, glycerin fatty acid esters and polyoxyethylene derivatives, and an ink composition containing a nonionic surfactant selected from these groups is preferred.
本発明で用いるカチオン系界面活性剤としては、脂肪族アミン塩、脂肪族４級アンモニウム塩、バンザルコニウム塩、ビリジニウム塩及びイミダゾリウム塩を例示することができ、これらの群から選ばれるカチオン系界面活性剤を含むインキ組成物が好ましい。 Examples of the cationic surfactant used in the present invention include aliphatic amine salts, aliphatic quaternary ammonium salts, vanzarconium salts, biridinium salts, and imidazolium salts, and cationic surfactants selected from these groups An ink composition containing an agent is preferred.
ノニオン系又はカチオン系界面活性剤は、既述の通り、インキ組成物全量に対して０．２〜２０重量％、好ましくは０．５〜１０重量％、より好ましくは顕色剤０．２〜２０重量％に対して０．２〜２０重量％、さらに好適には０．５〜１０重量％含ませることが好ましい。上記界面活性剤を０．２〜２０重量％、好ましくは０．５〜１０重量％の量的範囲内で含有量を調節することにより、経時消去性の速度を制御することができ、界面活性剤の含有量を多くすることにより経時消去性の速度を早くすることができ、界面活性剤の含有量を少なくすることにより経時消去性の速度を遅延させることができる。上記界面活性剤が０．２重量％未満では消去し難く、２０重量％を超えると発色濃度が薄くなる。 As described above, the nonionic or cationic surfactant is 0.2 to 20% by weight, preferably 0.5 to 10% by weight, more preferably 0.2 to 0.2% of the developer based on the total amount of the ink composition. It is preferable to contain 0.2 to 20% by weight, more preferably 0.5 to 10% by weight with respect to 20% by weight. By adjusting the content of the surfactant in a quantitative range of 0.2 to 20% by weight, preferably 0.5 to 10% by weight, the erasability with time can be controlled, and the surface activity Increasing the content of the agent can increase the erasability with time, and decreasing the surfactant content can delay the erasability with time. If the surfactant is less than 0.2% by weight, it is difficult to erase, and if it exceeds 20% by weight, the color density is reduced.
本発明は水溶性樹脂を用いることができる。例えばポリビニルピロリドン、セルロース系樹脂などを用いることができ、具体的にはポリビニルピロリドン、ヒドロキシブロピルセルロースを好ましく用いることができる。本発明のインキ組成物にこれらの水溶性樹脂を用いて造膜することにより、筆跡中に有機溶剤が残ったときのノビを防止し、さらに樹脂そのものが水溶性であるため、水に対する消去性が向上する。従って、筆記後自然に消去する過程で、強制的に水により消去する機能も兼備することができる。 In the present invention, a water-soluble resin can be used. For example, polyvinyl pyrrolidone and cellulose resin can be used. Specifically, polyvinyl pyrrolidone and hydroxypropyl cellulose can be preferably used. By forming a film using these water-soluble resins in the ink composition of the present invention, nodding when an organic solvent remains in the handwriting is prevented, and furthermore, since the resin itself is water-soluble, it is erasable to water. Will improve. Accordingly, it is possible to have a function of forcibly erasing with water in the process of erasing naturally after writing.
上記水溶性樹脂は、インキ組成物全量に対して１〜２０重量％含ませることができ、好ましい含有量は２〜１０重量％である。１重量％以上含有することにより、水による消去性が向上する。上記水溶性樹脂がインキ組成物全量に対して２０重量％を超えると、水により消去し難くなる。 The water-soluble resin can be contained in an amount of 1 to 20% by weight based on the total amount of the ink composition, and the preferred content is 2 to 10% by weight. By containing 1% by weight or more, the erasability with water is improved. When the water-soluble resin exceeds 20% by weight based on the total amount of the ink composition, it becomes difficult to erase with water.
なお、水消去性の向上を求めないインキ組成物の場合では、油溶性樹脂を用いることができる。例えばフェノール樹脂、アクリル樹脂、マレイン酸樹脂、ポリ塩化ビニル樹脂などである。 In the case of an ink composition that does not require improvement in water erasability, an oil-soluble resin can be used. For example, phenol resin, acrylic resin, maleic acid resin, polyvinyl chloride resin and the like.
本発明で用いる有機溶剤としては、任意に選定できるが、ロイコ染料その他成分の溶解性や筆跡の乾燥速度を考慮して選定することが好ましい。揮発性有機溶剤が好ましい。アルコール系、セロソルブ系グリコールエーテル系、エステル系等を例示することができる。具体的には、イソプロピルアルコール、ブタノール、プロピレングリコールモノメチルエーテルなどを用いることができる。なお、上記有機溶剤は、インキ組成物中、残りの成分（残部）含有量として配合することができる。 The organic solvent used in the present invention can be arbitrarily selected, but is preferably selected in consideration of the solubility of the leuco dye and other components and the drying speed of the handwriting. Volatile organic solvents are preferred. Examples include alcohols, cellosolve glycol ethers, and esters. Specifically, isopropyl alcohol, butanol, propylene glycol monomethyl ether, or the like can be used. In addition, the said organic solvent can be mix | blended as remaining component (remainder) content in an ink composition.
また、湿潤剤として、ポリエチレングリコール、グリセリン、プロピレングリコールなどを配合することができる。 Moreover, polyethylene glycol, glycerin, propylene glycol, etc. can be mix | blended as a wetting agent.
下記表１に示す組成にて、ロイコ染料、顕色剤、水溶性樹脂を有機溶剤に添加し、攪拌溶解させて、実施例及び比較例に係るインキ組成物を得た。 In the composition shown in Table 1 below, a leuco dye, a developer, and a water-soluble resin were added to an organic solvent and dissolved by stirring to obtain ink compositions according to Examples and Comparative Examples.
次に、上記実施例、比較例の各インキ組成物をポリエステル繊維束からなる中芯に充填し、マーキングペンを作成し、筆記後の経時消去性及び水消去性についてそれぞれ評価した。 Next, each ink composition of the above Examples and Comparative Examples was filled into a core made of a polyester fiber bundle to prepare a marking pen, and evaluated with respect to erasability over time and water erasability after writing.
＜評価＞
（経時消色性）
実施例及び比較例の各インキが充填された上記マーキングペンを用いて、ホーロー製のホワイトボード、杉板、ケント紙にそれぞれ筆記し、筆記1日後の消色度合いを確認した。
○：完全に消色
△：薄く筆跡が残る
×：消色しない
<Evaluation>
(Decolorization with time)
Using the marking pens filled with the inks of Examples and Comparative Examples, writing was made on a white board, cedar board, and Kent paper made by enamel, and the degree of decoloration after one day of writing was confirmed.
○: Completely decolored △: Thin handwriting remains ×: No decolorization
（水消去性）
実施例及び比較例の各インキが充填された上記マーキングペンを用いて、ホーロー製のホワイトボード、杉板、ケント紙にそれぞれ筆記する。筆記後、水を含ませた布で筆跡を消去する。
○：綺麗に消去出来る
△：筆跡の一部が残る
×：消去されない
(Water erasability)
Using the above-described marking pens filled with the respective inks of Examples and Comparative Examples, writing is made on a white board, cedar board, and Kent paper made by enamel. After writing, erase the handwriting with a cloth soaked in water.
○: Clearly erased △: Part of the handwriting remains ×: Not erased
表１より、界面活性剤を含まないインキ組成物は経時消去性が発揮しないが、界面活性剤を含むインキ組成物は、杉板、ケント紙のような吸収面やホワイトボードのような非吸収面の両者に対しすぐれた経時消去性を発揮していることが認められる。特に、界面活性剤が０．２重量％を含む実施例１０に対して、同界面活性剤を２０重量％含むインキの場合、消去速度が早かった。なお、水溶性樹脂を含む実施例８、９の場合、他の実施例と比較して水消去性が向上していた。 From Table 1, the ink composition containing no surfactant does not exhibit erasability over time, but the ink composition containing the surfactant has an absorbent surface such as cedar board and Kent paper and a non-absorbent surface such as whiteboard. It can be seen that both exhibit excellent erasability over time. In particular, with respect to Example 10 in which the surfactant contained 0.2% by weight, the erasing speed was faster in the case of the ink containing 20% by weight of the surfactant. In Examples 8 and 9 containing a water-soluble resin, water erasability was improved as compared with other examples.
本発明は、金属、ガラスなど非吸収面のみならず、木材、紙、石膏ボードなどの吸収面に筆記又は塗布しても、筆跡は当初鮮明に発色するが、自然に発色状態から無色に変化して経時的に消去することから、マーキングペンなどの筆記具のほか、特に、墨壷用墨汁等の墨壷用インキとして好適に用いることができる。
In the present invention, not only non-absorbing surfaces such as metal and glass, but also writing or coating on absorbing surfaces such as wood, paper and gypsum board, the handwriting initially develops a clear color, but naturally changes from a colored state to colorless. Therefore, the ink can be suitably used as a writing ink such as a marking pen, and particularly as ink for ink brushes such as ink for ink.
Claims (7)
ｉ） ロイコ染料 ０．１〜５重量％
ｉｉ） 顕色剤 ０．２〜２０重量％
ｉｉｉ）ノニオン系又はカチオン系界面活性剤 ０．２〜２０重量％
ｉＶ） 水溶性樹脂 １〜２０重量％
Ｖ） 有機溶剤 残部 A time-erasable ink composition containing the following components based on the total amount of the ink composition.
i) 0.1 to 5% by weight of leuco dye
ii) Developer 0.2 to 20% by weight
iii) Nonionic or cationic surfactant 0.2 to 20% by weight
iV) Water-soluble resin 1-20% by weight
V) Organic solvent balance
An ink brush ink comprising the ink composition according to any one of claims 1 to 6.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007004629A1 (en) * | 2005-07-06 | 2007-01-11 | Sakura Color Products Corporation | Water-erasable ink composition |
| EP2604657A4 (en) * | 2010-08-11 | 2015-08-19 | Kyowa Medex Co Ltd | Method for preserving aqueous solution containing leuco chromogen |
| JP2017002177A (en) * | 2015-06-10 | 2017-01-05 | 三夫 木本 | Erasable ink composition and manufacturing method therefor and fixation liquid thereof |
| CN110806387A (en) * | 2019-11-12 | 2020-02-18 | 中国刑事警察学院 | Method for judging formation time of iron tannate ink handwriting |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007004629A1 (en) * | 2005-07-06 | 2007-01-11 | Sakura Color Products Corporation | Water-erasable ink composition |
| EP2604657A4 (en) * | 2010-08-11 | 2015-08-19 | Kyowa Medex Co Ltd | Method for preserving aqueous solution containing leuco chromogen |
| US9493433B2 (en) | 2010-08-11 | 2016-11-15 | Kyowa Medex Co., Ltd. | Method for preserving aqueous solution containing leuco chromogen |
| JP2017002177A (en) * | 2015-06-10 | 2017-01-05 | 三夫 木本 | Erasable ink composition and manufacturing method therefor and fixation liquid thereof |
| CN110806387A (en) * | 2019-11-12 | 2020-02-18 | 中国刑事警察学院 | Method for judging formation time of iron tannate ink handwriting |
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