JPH0536720Y2 - - Google Patents

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Publication number
JPH0536720Y2
JPH0536720Y2 JP1987091050U JP9105087U JPH0536720Y2 JP H0536720 Y2 JPH0536720 Y2 JP H0536720Y2 JP 1987091050 U JP1987091050 U JP 1987091050U JP 9105087 U JP9105087 U JP 9105087U JP H0536720 Y2 JPH0536720 Y2 JP H0536720Y2
Authority
JP
Japan
Prior art keywords
photochromic
temperature
dependent
compound
color
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP1987091050U
Other languages
Japanese (ja)
Other versions
JPS63198599U (en
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to JP1987091050U priority Critical patent/JPH0536720Y2/ja
Publication of JPS63198599U publication Critical patent/JPS63198599U/ja
Application granted granted Critical
Publication of JPH0536720Y2 publication Critical patent/JPH0536720Y2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Inks, Pencil-Leads, Or Crayons (AREA)

Description

【考案の詳細な説明】 産業上の利用分野 本考案は温度依存性を有するホトクロミツク組
成物を応用した装飾体に関する。
[Detailed Description of the Invention] Industrial Application Field The present invention relates to a decorative body using a temperature-dependent photochromic composition.

従来の技術 従来、スピロピランなどの有機ホトクロミツク
化合物の応用化が試みられていたが、光照射によ
る劣化が著しく実用に至つていない。
Prior Art Conventionally, attempts have been made to apply organic photochromic compounds such as spiropyran, but they have not been put to practical use because of their significant deterioration due to light irradiation.

また耐光性により優れたスピロオキサジンにお
いては多数のコーテイング組成物などが提案され
ているが、温度依存性を有するようなホトクロミ
ツク材料及びその応用については提案されていな
い。
Furthermore, many coating compositions have been proposed for spirooxazine, which has excellent light resistance, but no photochromic materials having temperature dependence and their applications have been proposed.

考案が解決しようとする問題点 従来、耐光性に優れたスピロオキサジン化合物
を用いたコーテイング材料は数多く提案されてい
るが、これらコーテイング材料により塗装された
物品のホトクロミツク機能は紫外線または太陽光
照射により発色し、更に暗所にて復色するという
単純な色変化を示すものである。
Problems that the invention aims to solve Many coating materials using spirooxazine compounds with excellent light resistance have been proposed, but the photochromic function of articles coated with these coating materials does not develop color when exposed to ultraviolet rays or sunlight. However, it shows a simple color change in which the color is restored in a dark place.

本考案は光照射と温度変化の両方の作用に反応
して多用の色変化を可逆的に示すホトクロミツク
装飾体を提供しようとするものである。
The present invention seeks to provide a photochromic decoration that reversibly exhibits multiple color changes in response to the effects of both light irradiation and temperature changes.

問題点を解決するための手段 本考案のホトクロミツク装飾体は所定の温度以
下でのみホトクロミツク性を示し、前記温度を越
えるとホトクロミツク性を示さないという温度依
存性を有するホトクロミツク顔料を含有するイン
キまたは塗料による塗布層を基体表面の全体また
は特定部分に設けてなつている。
Means for Solving the Problems The photochromic decoration of the present invention is an ink or paint containing a photochromic pigment that exhibits photochromic properties only at a predetermined temperature or below and does not exhibit photochromic properties above the above temperature. The coating layer is applied to the entire surface of the substrate or to a specific part of the substrate.

本考案に用いられる基体としては布、プラスチ
ツクス、紙、ガラス、金属、セラミツクス等の材
料からなる物があげられる。
Substrates used in the present invention include those made of materials such as cloth, plastics, paper, glass, metal, and ceramics.

前記ホトクロミツク顔料は先に本出願人が提案
したスピロオキサジン化合物と沸点150℃以上の
有機媒質化合物からなる温度依存性ホトクロミツ
ク組成物を公知の手法で微小カプセル化して得ら
れるものである。
The photochromic pigment is obtained by microcapsulating a temperature-dependent photochromic composition, which is composed of a spirooxazine compound previously proposed by the applicant and an organic medium compound having a boiling point of 150° C. or higher, by a known method.

前記スピロオキシサジン化合物としては1,
3,3−トリメチル−スピロインドリンナフトオ
キサジン、1,3,3−トリメチル−5−クロロ
−スピロインドリンナフトオキサジン及び1,
3,3−トリメチル−スピロフエナトロオキサジ
ン等が挙げられ、沸点150℃以上の有機媒体質化
合物としてはアルコール類、エステル類、ケトン
類、カルボン酸類、酸アミド類、エーテル類、ア
ゾメチン類、スルフイド類、芳香族炭化水素類、
及び脂肪族炭化水素類から選ばれる化合物があげ
られる。具体的な化合物名としてセチルアルコー
ル、ステアリン酸、ラウリン酸ラウリル、ステア
リン酸アマイド等を例示することができる。
The spirooxysazine compound is 1,
3,3-trimethyl-spiroindolinenaphthoxazine, 1,3,3-trimethyl-5-chloro-spiroindolinenaphthoxazine and 1,
Examples include 3,3-trimethyl-spirophenatrooxazine, and organic medium compounds with a boiling point of 150°C or higher include alcohols, esters, ketones, carboxylic acids, acid amides, ethers, azomethines, and sulfides. , aromatic hydrocarbons,
and aliphatic hydrocarbons. Specific compound names include cetyl alcohol, stearic acid, lauryl laurate, stearamide, and the like.

前記組成物が微小カプセル化されてなるホトク
ロミツク顔料はカプセル壁膜の隔離作用により、
スピロオキサジン化合物と有機媒質化合物の分離
を抑止し、温度依存性をもつホトクメミツク組成
物を所定の媒体中に保持できる利点がある。
The photochromic pigment obtained by encapsulating the above composition has the following properties:
There is an advantage that separation of the spirooxazine compound and the organic medium compound can be suppressed, and a temperature-dependent photoluminescent composition can be maintained in a predetermined medium.

ホトクロミツク塗布層は前記ホトクロミツク顔
料を高分子樹脂溶液または樹脂エマルシヨンに混
合、分散して得られるインキまたは塗料を刷毛
塗、スプレー塗布、スクリーン印刷、グラビア印
刷、捺染等の方法により基体表面に形成される。
The photochromic coating layer is formed on the surface of the substrate by a method such as brush coating, spray coating, screen printing, gravure printing, or textile printing with an ink or paint obtained by mixing and dispersing the photochromic pigment in a polymer resin solution or resin emulsion. .

更に必要に応じて、前記塗布層表面に耐摩耗
性、耐水性等の物理的強度及び耐光性の向上を目
的として、保護層を設けてもよい。
Furthermore, if necessary, a protective layer may be provided on the surface of the coating layer for the purpose of improving physical strength such as abrasion resistance and water resistance, and light resistance.

尚、前記インキまたは塗料には通常の染顔料、
体質顔料、紫外線吸収剤、酸化防止剤、老化防止
剤などが添加されていてもよく、また前記塗布量
には不変色の図柄層が併設されてもよい。
The ink or paint may contain ordinary dyes and pigments,
Extender pigments, ultraviolet absorbers, antioxidants, anti-aging agents, etc. may be added, and a colorless pattern layer may also be added to the coating amount.

前記塗布層のホトクロミツク特性の発現を左右
する温度は、用いられるホトクロミツク顔料の有
機媒化合物によつて調節可能であるが、概略10乃
至50℃の温度範囲で所定の温度を設定できる。
The temperature which influences the development of the photochromic properties of the coating layer can be adjusted depending on the organic medium compound of the photochromic pigment used, and a predetermined temperature can be set within the temperature range of approximately 10 to 50°C.

作 用 本考案のホトクロミツク装飾体の塗布層は紫外
線や太陽光の照射に応じて色変化を起こすばかり
でなく、温度変化によつても前記光照射による色
変化の生起を制御できるので、光照射と温度変化
を組み合わせて適用することにより、多段の色変
化を繰り返して展開させることができる。また基
体表面の特定部分毎にホトクロミズム生起温度が
異なる種類のホトクロミツク組成物を含む塗布層
を設けれは、更に多用の色変化を生起する装飾体
となる。
Effect: The coating layer of the photochromic decoration of the present invention not only changes color in response to irradiation with ultraviolet rays or sunlight, but also can control the color change caused by the light irradiation due to temperature changes. By applying this in combination with temperature changes, it is possible to repeatedly develop multi-stage color changes. Furthermore, if a coating layer containing a photochromic composition having a different photochromic initiation temperature is provided for each specific portion of the substrate surface, the decorative body will be able to exhibit even more color changes.

実施例 1,3,3−トリメチルスピロインドリンナフ
トオキサジン2g、制御散るアルコール30g、ラ
ウリン酸ステアリル20g及びエポキシ樹脂(エピ
コート807、油化シエル社製)12gを120℃にて均
一相溶させ、80℃にて溶液状態に保つた。
Example 2 g of 1,3,3-trimethylspiroindoline naphthoxazine, 30 g of controlled dispersion alcohol, 20 g of stearyl laurate, and 12 g of epoxy resin (Epicote 807, manufactured by Yuka Ciel Co., Ltd.) were uniformly dissolved at 120°C, and then mixed at 80°C. The solution was kept in solution.

別に15%アラビアガム水溶液100gを調製し、
70℃に保ちながら前記溶液をホモミキサーを用い
て平均粒子径5μmに乳化し、ジエチレントリアミ
ン3gを徐々に滴下する。更に3時間攪拌を続け
た後、生成した微小カプセル形態のホトクロミツ
ク顔料を遠心分離した。
Separately, prepare 100g of 15% gum arabic aqueous solution,
While maintaining the temperature at 70°C, the solution was emulsified to an average particle size of 5 μm using a homomixer, and 3 g of diethylenetriamine was gradually added dropwise. After continuing stirring for an additional 3 hours, the produced photochromic pigment in the form of microcapsules was centrifuged.

このホトクロミツク顔料を脱水乾燥後、適宜量
を塩化ビニル−酢酸ビニル共重合体樹脂を含むビ
ビクルに均一分散し、溶剤で希釈してスプレー用
塗料を得た。
After dehydrating and drying this photochromic pigment, an appropriate amount was uniformly dispersed in a vehicle containing a vinyl chloride-vinyl acetate copolymer resin, and diluted with a solvent to obtain a spray paint.

前記塗料により表面塗装された、肌色に着色さ
れている塩化ゴニル製の人形は暗所では肌色を呈
しているが、外気温度25℃にて太陽光に曝したと
ころ瞬時に暗褐色に変化し、日焼けした肌の様相
を呈した。次いで太陽光に曝しながら、約35℃の
息を吹きかけたところ、ほぼ瞬時にもとの肌色に
戻つた。再び25度の外気温に放置しておくと暗褐
色となり、暗所に戻せば肌色となつた。この変化
は繰り返し行うことができた。
A doll made of gonyl chloride whose surface is painted with the above-mentioned paint has a flesh-colored appearance in the dark, but when exposed to sunlight at an outside temperature of 25 degrees Celsius, it instantly changes to dark brown. It gave the appearance of tanned skin. When I then exposed it to sunlight and breathed on it at about 35 degrees Celsius, it almost instantly returned to its original skin color. When I left it at an outside temperature of 25 degrees again, it turned dark brown, and when I returned it to the dark, it became a skin color. This change could be repeated.

尚、本実施例に用いてホトクロミツク顔料は30
℃未満でのみホトクロミズムを示し、30℃以上で
はホトクロミズムを示さない特性をもつ。
The photochromic pigment used in this example was 30
It exhibits photochromism only at temperatures below ℃ and does not exhibit photochromism above 30℃.

考案の効果 本考案のホトクロミツク装飾体は従来のものに
較べ、温度依存性を有しているので、光照射と温
度変化の組合せにより、より複合的な外観変化を
延出させることができ、玩具、衣料、日用品をは
じめ調光材料、書籍、偽造防止、デイスプレー用
など幅広い応用展開ができる。
Effects of the invention The photochromic decoration of the invention is more temperature-dependent than conventional ones, so a combination of light irradiation and temperature changes can produce more complex changes in appearance, making it possible to create toys. It can be used in a wide range of applications, including clothing, daily necessities, light control materials, books, anti-counterfeiting, and display displays.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本考案のホトクロミツク人形の条件1
所定温度未満での光照射下の状態1と条件2所定
温度以上での光照射下及び条件3暗所に置いた状
態2を表している。
Figure 1 shows conditions 1 for the photochromic doll of the present invention.
State 1 is under light irradiation at a temperature below a predetermined temperature, Condition 2 is under light irradiation at a temperature above a predetermined temperature, and Condition 3 is State 2 in a dark place.

Claims (1)

【実用新案登録請求の範囲】[Scope of utility model registration request] 基体表面の全体または特定部分に、(イ)スピロナ
フトオキサジン化合物と(ロ)アルコール類、エステ
ル類、ケトン類、カルボン酸類、酸アミド類、エ
ーテル類、アゾメチン類、スルフイド類、芳香族
炭化水素類及び脂肪族炭化水素類から選ばれる沸
点150℃以上の有機媒質化合物からなる温度依存
性ホトクロミツク組成物を内蔵した微小カプセル
を含有するインキまたは塗料が塗布されてなる温
度依存性ホトクロミツク装飾体。
(a) Spironaphthoxazine compound and (b) alcohols, esters, ketones, carboxylic acids, acid amides, ethers, azomethines, sulfides, and aromatic hydrocarbons on the entire or specific portion of the substrate surface. A temperature-dependent photochromic decoration coated with an ink or paint containing microcapsules containing a temperature-dependent photochromic composition comprising an organic medium compound with a boiling point of 150° C. or higher selected from aliphatic hydrocarbons and aliphatic hydrocarbons.
JP1987091050U 1987-06-13 1987-06-13 Expired - Lifetime JPH0536720Y2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1987091050U JPH0536720Y2 (en) 1987-06-13 1987-06-13

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1987091050U JPH0536720Y2 (en) 1987-06-13 1987-06-13

Publications (2)

Publication Number Publication Date
JPS63198599U JPS63198599U (en) 1988-12-21
JPH0536720Y2 true JPH0536720Y2 (en) 1993-09-16

Family

ID=30951476

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1987091050U Expired - Lifetime JPH0536720Y2 (en) 1987-06-13 1987-06-13

Country Status (1)

Country Link
JP (1) JPH0536720Y2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5257979B2 (en) * 2008-06-06 2013-08-07 学校法人同志社 An effect system comprising an expression mode and / or a pattern change by a combination of a color material and illumination

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61276882A (en) * 1985-06-03 1986-12-06 Unitika Ltd Photochromic laminate
JPH0730317B2 (en) * 1985-07-23 1995-04-05 ユニチカ株式会社 Photochromic composition with excellent color development

Also Published As

Publication number Publication date
JPS63198599U (en) 1988-12-21

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