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JPH0513074B2 - - Google Patents
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JPH0513074B2 - - Google Patents

Info

Publication number
JPH0513074B2
JPH0513074B2 JP59117389A JP11738984A JPH0513074B2 JP H0513074 B2 JPH0513074 B2 JP H0513074B2 JP 59117389 A JP59117389 A JP 59117389A JP 11738984 A JP11738984 A JP 11738984A JP H0513074 B2 JPH0513074 B2 JP H0513074B2
Authority
JP
Japan
Prior art keywords
dye
recording
group
sheet
formula
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 - Fee Related
Application number
JP59117389A
Other languages
Japanese (ja)
Other versions
JPS60260391A (en
Inventor
Toshio Niwa
Jukichi Murata
Shuichi Maeda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Industries Ltd
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 by Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Chemical Industries Ltd
Priority to JP59117389A priority Critical patent/JPS60260391A/en
Priority to US06/733,222 priority patent/US4614521A/en
Priority to CA000481468A priority patent/CA1227034A/en
Priority to GB08512409A priority patent/GB2159971B/en
Priority to FR858507587A priority patent/FR2565528B1/en
Priority to DE19853520227 priority patent/DE3520227A1/en
Publication of JPS60260391A publication Critical patent/JPS60260391A/en
Publication of JPH0513074B2 publication Critical patent/JPH0513074B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/385Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5227Macromolecular coatings characterised by organic non-macromolecular additives, e.g. UV-absorbers, plasticisers, surfactants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/385Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B41M5/3852Anthraquinone or naphthoquinone dyes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/385Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B41M5/3854Dyes containing one or more acyclic carbon-to-carbon double bonds, e.g., di- or tri-cyanovinyl, methine
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/385Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B41M5/3856Dyes characterised by an acyclic -X=C group, where X can represent both nitrogen and a substituted carbon atom
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/385Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B41M5/388Azo dyes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/385Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B41M5/39Dyes containing one or more carbon-to-nitrogen double bonds, e.g. azomethine
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5245Macromolecular coatings characterised by the use of polymers containing cationic or anionic groups, e.g. mordants

Landscapes

  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

発明の目的 (イ) 産業上の利用分野 本発明は、支持体上に色素層を有する転写シー
トと、基体上に記録層を有する被記録体シートと
からなる感熱記録用シート・セツトに関するもの
である。 (ロ) 従来の技術 近年急速に普及しつつあるフアクシミリ、プリ
ンタ、複写機等のOA端末機においては、情報量
を多く含み、かつ視覚的にも見易いカラー記録の
要望が高まつている。一方テレビ画像をカラー記
録化する技術の開発が望まれている。 現在、これらの目的のために、電子写真、イン
クジエツト、感熱転写方式によるカラー記録技術
が検討されている。 これらの中にあつて感熱転写方式は装置の保
守、操作性が容易で装置及び消耗品が安価である
ため他の方法に比べ有利である。 感熱転写の方式には支持体上に形成した色素層
を感熱ヘツドにより加熱溶融して被記録体上に転
写記録する溶融方式と、支持体上に昇華性色素を
含む色素層を形成し、感熱ヘツドにより加熱し色
素を昇華させ被記録体上に転写記録する昇華方式
とがあるが、昇華方式は感熱ヘツドに与えるエネ
ルギーを変えることにより、色素の昇華転写量を
制御することができるので階調記録が容易でフル
カラー記録には特に有利と考えられる。 上記昇華方式で使用する色素は感熱ヘツドの負
担を小さくするため、また記録速度をあげるため
できる限り昇華し易い色素が望ましいが、昇華し
易い色素は、長期の保在中あるいは高温及び高湿
の環境下において、被記録体から色素が再昇華し
記録が劣化したり、接触物に移行し汚染したりし
て転写後の記録の保守安定性に問題があつた。 かかる問題を解決する方法として、転写記録
後、被記録体の表面を樹脂フイルムでラミネート
することにより再昇華を防ぐことが考えられる。 しかしながら、かかる方法においては、ラミネ
ートするための材料と装置が必要であり、装置全
体が大型化、複雑化するため更に改良が望まれて
いる。 (ハ) 目的 本発明は、保存安定性の優れた転写記録を得る
ための、転写シートと被記録体シートからなる感
熱記録用シート・セツトを提供することを目的と
するものである。 発明の構成 本発明は支持体上に色素層を有する転写シート
と、基体上に記録層を有する被記録体シートから
なる感熱記録用シート・セツトであり、色素層が
エポキシ基を有する色素を含有し、記録層が活性
水素化合物または有機酸無水物を含有する感熱記
録用シート・セツトをその要旨とするものであ
る。 本発明で使用するエポキシ基を有する色素とし
ては、アゾ系、アントラキノン系、ナフトキノン
系、キノフタロン系、スチリル系、アゾメチン系
などの色素の内で該エポキシ基を有する色素が挙
げられる。 (1) アゾ系色素としては、一般式() (式中、A1は置換基を有していてもよいフエ
エル基、ベンゾチアゾール基、イミダゾール基ま
たはチエニル基を表わし、R1は水素原子、アル
キル基またはアルキルカルボニルアミノ基を表わ
し、R2はアルキル基を表わす。)で示されるアゾ
系色素等が挙げられる。 具体的には、例えば、下記の様なものが挙げら
れる。 (2) アントラキノン系色素としては、例えば、一
般式()又は一般式() (式中、R3及びR4は水素原子、アルキル基ま
たは
Object of the Invention (a) Industrial Application Field The present invention relates to a heat-sensitive recording sheet set comprising a transfer sheet having a dye layer on a support and a recording sheet having a recording layer on the base. be. (b) Prior Art In office automation terminals such as facsimile machines, printers, and copiers, which have become rapidly popular in recent years, there is a growing demand for color recording that contains a large amount of information and is visually easy to read. On the other hand, it is desired to develop a technology for recording television images in color. Currently, color recording techniques using electrophotography, inkjet, and thermal transfer systems are being considered for these purposes. Among these methods, the thermal transfer method is advantageous over other methods because the device is easy to maintain and operate, and the device and consumables are inexpensive. Thermal transfer methods include the melting method, in which a dye layer formed on a support is heated and melted by a heat-sensitive head, and transferred and recorded onto the recording medium, and the other is a heat-sensitive transfer method, in which a dye layer containing a sublimable dye is formed on a support. There is a sublimation method, in which the dye is heated by a head to sublimate it and then transferred and recorded onto the recording medium.With the sublimation method, the amount of sublimation and transfer of the dye can be controlled by changing the energy given to the heat-sensitive head, resulting in gradation. It is easy to record and is considered to be particularly advantageous for full-color recording. It is desirable that the dye used in the above sublimation method be one that sublimates as easily as possible in order to reduce the burden on the heat-sensitive head and increase the recording speed. Under environmental conditions, the dye re-sublimates from the recording material, deteriorating the recording, or transfers to a contact object, causing contamination, which poses problems in the maintenance stability of the recording after transfer. One possible solution to this problem is to laminate the surface of the recording medium with a resin film after transfer recording to prevent re-sublimation. However, such a method requires materials and equipment for laminating, and the entire equipment becomes larger and more complicated, so further improvements are desired. (C) Objective The object of the present invention is to provide a heat-sensitive recording sheet set consisting of a transfer sheet and a recording material sheet for obtaining transfer recording with excellent storage stability. Structure of the Invention The present invention is a heat-sensitive recording sheet set consisting of a transfer sheet having a dye layer on a support and a recording material sheet having a recording layer on the substrate, the dye layer containing a dye having an epoxy group. However, the gist thereof is a heat-sensitive recording sheet set whose recording layer contains an active hydrogen compound or an organic acid anhydride. The epoxy group-containing dye used in the present invention includes azo-, anthraquinone-, naphthoquinone-, quinophthalone-, styryl-, and azomethine-based dyes having the epoxy group. (1) As an azo dye, the general formula () (In the formula, A 1 represents a fuel group, benzothiazole group, imidazole group, or thienyl group that may have a substituent, R 1 represents a hydrogen atom, an alkyl group, or an alkylcarbonylamino group, and R 2 represents a hydrogen atom, an alkyl group, or an alkylcarbonylamino group. Representing an alkyl group), azo dyes and the like can be mentioned. Specifically, for example, the following may be mentioned. (2) As an anthraquinone dye, for example, general formula () or general formula () (In the formula, R 3 and R 4 are hydrogen atoms, alkyl groups, or

【式】で示される基を表わ し、R5は水素原子または
Represents a group represented by [Formula], R 5 is a hydrogen atom or

【式】で示される基を表 わし、R6及びR7は水素原子またはアルキル基を
表わす。但し、R3及びR4が同時に水素原子また
はアルキル基のとき、R5
It represents a group represented by the formula: R 6 and R 7 represent a hydrogen atom or an alkyl group. However, when R 3 and R 4 are both hydrogen atoms or alkyl groups, R 5 is

【式】で示される基を表 わす。)で示されるアントラキノン系色素等が挙
げられる。 具体的には例えば、下記の様なものが挙げられ
る。 (3) ナフトキノン系色素としては、例えば、一般
式()又は一般式() (式中、R3は水素原子、アルキル基または
Represents a group represented by [Formula]. ) and the like are mentioned. Specific examples include the following. (3) As naphthoquinone dyes, for example, general formula () or general formula () (In the formula, R 3 is a hydrogen atom, an alkyl group, or

【式】で示される基を表わす。) で示されるナフトキノン系色素等が挙げられる。 具体的には、例えば、下記の様なものが挙げら
れる。 (4) キノフタロン系色素としては、例えば、一般
式() (式中、−X−は−O−または−NH−を表わ
す。)で示されるキノフタロン系色素等が挙げら
れる。 具体的は、例えば、下記の様なものが挙げられ
る。 (5) スチリル系色素としては、例えば、一般式
() (式中、R9は水素原子またはシアノ基を表わ
し、R1及びR2は前記と同義を表わす。)で示され
るスチリル系色素等が挙げられる。 具体的には、例えば、下記の様なものが挙げら
れる。 (6) アゾメチン系色素としては、例えば、一般式
() (式中、A2
Represents a group represented by [Formula]. ) Examples include naphthoquinone dyes shown in the following. Specifically, for example, the following may be mentioned. (4) Quinophthalone dyes include, for example, the general formula () (In the formula, -X- represents -O- or -NH-.) Quinophthalone dyes and the like can be mentioned. Specifically, for example, the following may be mentioned. (5) As styryl dyes, for example, general formula () (In the formula, R 9 represents a hydrogen atom or a cyano group, and R 1 and R 2 have the same meanings as above.) Styryl dyes and the like can be mentioned. Specifically, for example, the following may be mentioned. (6) As the azomethine dye, for example, the general formula () (In the formula, A 2 is

【式】【formula】

【式】【formula】

【式】また は[Formula] Also teeth

【式】で示される基を表わし、 R10,R11及びR12はアルキル基を表わし、R13
水素原子またはアルキルアミノカルボニル基を表
わし、R1及びR2は前記と同義を表わす。)で示さ
れるアゾメチン系色素等が挙げられる。 具体的には、例えば、下記の様なものが挙げら
れる。 次に転写シートの作成方法について説明する。 転写シートは、前記の色素を適当な樹脂および
溶剤、水などと混合し、インキを調製し、そのイ
ンキを適当な支持体上に塗布後乾燥し、色素層を
形成することにより得ることができる。 上記のインキを調製するための樹脂としては、
融点あるいは軟化点の高いものが適当であり、具
体的には次のようなものが挙げられる。 フエノール樹脂、メラミン樹脂、ウレタン樹
脂、エポキシ樹脂、シリコーン樹脂、ユリア樹
脂、ジアリルフタレート樹脂、アルキツド樹脂、
アセタール樹脂、アクリル樹脂、メタクリル樹
脂、ポリエステル樹脂、デンプンおよびその誘導
体、セルロース系樹脂、ポリ塩化ビニル、ポリ塩
化ビニリデン、フツ素樹脂、塩素化ポリエチレ
ン、ポリエチレン、ポリプロピレン、ポリスチレ
ン、ポリビニルアセタール、ポリアミド、ポリビ
ニルアルコール、ポリカーボネート、ポリスルホ
ン、ポリエーテルスルホン、ポリエチレンテレフ
タレート、ポリブチレンテレフタレート、ポリフ
エニレンオキシド、ポリフエニレンスルフイド、
ポリエチレンナフタレート・ポリアクリロニトリ
ル、ポリイミド、ポリアミド、AS樹脂、ABS樹
脂。 特に好ましくは、ポリスルホン、ポリエーテル
スルホン、ポリエチレンテレフタレート、ポリカ
ーボネート等の不活性な樹脂が挙げられる。 又、インキ調製のための溶剤としては、メタノ
ール、エタノール、プロパノール、ブタノールな
どのアルコール類、メチルセロソルブ、エチルセ
ロソルブなどのセロソルブ類、ベンゼン、トルエ
ン、キシレン、クロロベンゼンなどの芳香族類、
酢酸エチル、酢酸ブチルなどのエステル類、アセ
トン、メチルエチルケトン、メチルイソブチルケ
トン、シクロヘキサノンなどのケトン類、リグロ
イン、シクロヘキサン、ケロシンなどの炭化水素
類、クロロホルム、塩化メチレン、トリクロロエ
チレンなどの塩素系溶剤、ジメチルホルムアミド
などが挙げられるが、水性系樹脂を使用する場合
には、水または水と上記の溶剤を混合して使用す
ることもできる。 特に好ましくはベンゼン、トルエン、キシレ
ン、クロロベンゼン、アセトン、メチルエチルケ
トン、クロロホルム、塩化メチレン等の不活性な
溶剤が挙げられる。 転写シートの支持体としては、コンデンサー
紙、グラシン紙のような薄葉紙、ポリエステル、
ポリアミド、ポリイミドのような耐熱性の良好の
プラスチツクのフイルムが適しているが、これら
の支持体は感熱記録ヘツドから色素等への伝熱効
率を良くするため薄くする必要があり、50μm以
下の厚さが適当であり好ましくは20μm以下のも
のが良い。 次に被記録体シートの作成方法について説明す
る。 本発明の被記録体シートは、適当な基体、例え
ば、紙、樹脂フイルム等の上に活性水素化合物ま
たは有機酸無水物を含む塗布液を塗布し、乾燥
し、記録層を形成することにより得られる。 その際、塗布液中にはポリエステル、ポリアミ
ド、ポリアクリル等の樹脂やシリカ、アルミナ、
炭酸カルシウムなどの無機微粒子等を添加しても
よい。 活性水素化合物としては、ヒドロキシル基、メ
ルカプト基、カルボキシル基、アミノ基、モノア
ルキルアミノ基、アミド基、好ましくは、ヒドロ
キシル基、カルボキシル基、アミノ基を有する公
知の種々の高分子化合物あるいは低分子化合物が
挙げられる。具体的な例としては以下のようなも
のが挙げられる。 (A) OH基を有する化合物 (B) メルカプト基を有する化合物
It represents a group represented by the formula: R 10 , R 11 and R 12 represent an alkyl group, R 13 represents a hydrogen atom or an alkylaminocarbonyl group, and R 1 and R 2 have the same meanings as above. ) and the like. Specifically, for example, the following may be mentioned. Next, a method for creating a transfer sheet will be explained. The transfer sheet can be obtained by mixing the above dye with a suitable resin, solvent, water, etc. to prepare an ink, and then coating the ink on a suitable support and drying it to form a dye layer. . As the resin for preparing the above ink,
Those having a high melting point or softening point are suitable, and specific examples include the following. Phenol resin, melamine resin, urethane resin, epoxy resin, silicone resin, urea resin, diallyl phthalate resin, alkyd resin,
Acetal resin, acrylic resin, methacrylic resin, polyester resin, starch and its derivatives, cellulose resin, polyvinyl chloride, polyvinylidene chloride, fluororesin, chlorinated polyethylene, polyethylene, polypropylene, polystyrene, polyvinyl acetal, polyamide, polyvinyl alcohol , polycarbonate, polysulfone, polyether sulfone, polyethylene terephthalate, polybutylene terephthalate, polyphenylene oxide, polyphenylene sulfide,
Polyethylene naphthalate/polyacrylonitrile, polyimide, polyamide, AS resin, ABS resin. Particularly preferred are inert resins such as polysulfone, polyethersulfone, polyethylene terephthalate, and polycarbonate. In addition, as solvents for ink preparation, alcohols such as methanol, ethanol, propanol, and butanol, cellosolves such as methyl cellosolve and ethyl cellosolve, aromatics such as benzene, toluene, xylene, and chlorobenzene,
Esters such as ethyl acetate and butyl acetate, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone, hydrocarbons such as ligroin, cyclohexane, and kerosene, chlorinated solvents such as chloroform, methylene chloride, and trichloroethylene, dimethyl formamide, etc. However, when using an aqueous resin, water or a mixture of water and the above-mentioned solvent can be used. Particularly preferred are inert solvents such as benzene, toluene, xylene, chlorobenzene, acetone, methyl ethyl ketone, chloroform, and methylene chloride. Supports for the transfer sheet include condenser paper, thin paper such as glassine paper, polyester,
Plastic films with good heat resistance such as polyamide and polyimide are suitable, but these supports need to be thin in order to improve the efficiency of heat transfer from the heat-sensitive recording head to the dye, and the thickness must be 50 μm or less. is suitable, and preferably 20 μm or less. Next, a method for creating a recording medium sheet will be explained. The recording medium sheet of the present invention can be obtained by applying a coating liquid containing an active hydrogen compound or an organic acid anhydride onto a suitable substrate, such as paper or resin film, and drying it to form a recording layer. It will be done. At that time, the coating solution contains resins such as polyester, polyamide, polyacrylic, silica, alumina, etc.
Inorganic fine particles such as calcium carbonate may also be added. Examples of the active hydrogen compound include various known high-molecular compounds or low-molecular compounds having a hydroxyl group, a mercapto group, a carboxyl group, an amino group, a monoalkylamino group, an amide group, preferably a hydroxyl group, a carboxyl group, or an amino group. can be mentioned. Specific examples include the following. (A) Compound with OH group (B) Compound with mercapto group

【式】【formula】

【式】【formula】

【式】 (C) カルボキシル基を有する化合物 (D) アミノ基、モノアルキル基、アミド基を有す
る化合物 H2NCH2CH2NH2 H2NCH2CH2NHCH2CH2NH2 (CH32NCH2CH2CH2NH2 HOCH2CH2NHCH2CH2NHCH2CH2OH H2NNHCO(CH24CONHNH2 (E) 異種の基を有する化合物 また、有機酸無水物としては、例えば、下記の
様なものが挙げられる。 上記で得られた転写シートおよび被記録体シー
トを用いて感熱転写記録を行なうのには、転写シ
ートのインキ塗布面と被記録体シートの塗布液塗
布面とを重ね合わせ、転写シートの背面から感熱
記録ヘツドで加熱加圧すれば良い。 発明の作用効果 上記の方法で転写記録を行なつた場合、転写シ
ートの色素層の色素が被記録体シート上に昇華転
写されると同時に、エポキシ基、を有する色素が
被記録体シートの記録層の活性水素化合物たとえ
ばヒドロキシル基、メルカプト基、カルボキシル
基、アミノ基、モノアルキルアミノ基、アミド基
を有する化合物あるいは有機酸無水物と反応する
ことにより、色素の定着が行なわれ、保存安定性
のすぐれた記録を得ることができると考えられ
る。 以上の説明及び後記実施例から明らかなよう
に、本発明により容易に保存安定性の優れた記録
を簡便に得ることができる。 以下実施例等によりこの発明を具体的に説明す
るが、かかる実施例は本発明を限定するものでは
ない。 実施例 実施例 1 1 転写シートの作成方法 上記構造式()色素 2g エチルセルロース 8gイソプロパノール 90g 計 100g 上記組成の混合物をガラスビーズを使用し、ペ
イントコンデイシヨナーで約30分間混合処理し、
インキの調製を行なつた。 上記のインキをグラビア校正機(版深30μm)
を用いコンデンサー紙(厚さ10μm)に塗布後自
然乾燥し、転写シートを作成した。 2 被記録体シートの作成方法 上記構造式()化合物 5g ポリエステル樹脂* 15gメチルエチルケトン 80g 計 100g * 東洋紡積株式会社製造“バイロン200”(商品
名) 上記組成物を混合し、塗布液を調製した。 上記の塗布液をグラビア校正機(版深30μm)
を用い上質紙に塗布後自然乾燥し被記録体シート
を作成した。 3 転写記録方法 上記転写シートのインキ塗布面を被記録体シー
トの塗布液塗布面と重ね、転写シートの背面から
感熱記録ヘツドを用いて加熱し、被記録体上に鮮
明な濃い橙色の記録を得ることができた。 このようにして得られた記録の安定性を試験す
るため記録面を上質紙と重ね合せ200g/cm2の圧
力下で80℃で24時間保持したが記録の色の変化及
び重ね合せた上質紙の色素による汚染はほとんど
なかつた。 参考例 1 (実施例1の色素の合成) N−エチルアニリン14g、エピクロルヒドリン
14.8g、水10ml、エタノール15mlを加え、水浴上
で3時間反応・攪拌した。冷却後、水液ロートで
分離し、硫酸ナトリウムで乾燥した。 得られたN−エチル−N−(2−オキシ−3−
クロロプロピル)アニリン21gを氷冷しながら、
50%−水酸化ナトリウム水溶液8mlを攪拌しなが
ら徐々に加えた。その後、4時間攪拌した後、生
成した塩化ナトリウムを別し、分液ロート中で
有機層を水洗後、硫酸ナトリウムで脱水した。 得られたN−エチル−N−グリシジルアニリン
とp−ニトロアニリンのジアゾ液とカツプリング
することにより下記構造式()で表わされる色
素を得た。 mp 159〜162℃ Massスペクトル M+326 λmax(クロロホルム) 474nm 比較例 1 1 転写シートの作成方法 実施例1と同様の方法により転写シートを作成
した。 2 被記録体シートの作成方法 ポリエステル樹脂(バイロン200)15gをメチ
ルエチルケトン85gに溶解したのみで実施例1に
おける化合物()を使用せずに塗布液を調製
し、実施例1と同様の方法により上質紙に塗布し
被記録体シートを作成した。 3 転写記録方法 上記の転写シートと被記録体シートとを重ね合
せ実施例1と同様の方法で転写記録を行ない濃い
黄色の記録を得た。 このようにして得られた記録について実施例1
と同様の方法により安定性の試験をした結果、重
ね合せた上質紙は被記録体シートからの色素の移
行により橙色に著しく汚染された。又被記録体シ
ートの色濃度も色素の移行により著しく低下し
た。 実施例 2 実施例1に示した色素のかわりに第1表に示す
構造式の色素を使用し、他は実施例1と同様の方
法により転写記録を実施し、保存安定性の良好な
記録を得ることができた。
[Formula] (C) Compound having a carboxyl group (D) Compounds having an amino group, monoalkyl group, or amide group H 2 NCH 2 CH 2 NH 2 H 2 NCH 2 CH 2 NHCH 2 CH 2 NH 2 (CH 3 ) 2 NCH 2 CH 2 CH 2 NH 2 HOCH 2 CH 2 NHCH 2 CH 2 NHCH 2 CH 2 OH H 2 NNHCO(CH 2 ) 4 CONHNH 2 (E) Compounds with different groups Furthermore, examples of organic acid anhydrides include the following. To perform thermal transfer recording using the transfer sheet and recording material sheet obtained above, the ink-coated surface of the transfer sheet and the coating liquid-coated surface of the recording material sheet are overlapped, and the back side of the transfer sheet is It can be heated and pressurized using a heat-sensitive recording head. Effects of the Invention When transfer recording is performed by the above method, the dye in the dye layer of the transfer sheet is sublimated and transferred onto the recording material sheet, and at the same time, the dye having an epoxy group is transferred to the recording material sheet. The dye is fixed by reacting with an active hydrogen compound in the layer, such as a compound having a hydroxyl group, a mercapto group, a carboxyl group, an amino group, a monoalkylamino group, an amide group, or an organic acid anhydride. It is thought that excellent records can be obtained. As is clear from the above explanation and the examples described later, records with excellent storage stability can be easily obtained by the present invention. EXAMPLES The present invention will be specifically explained below with reference to Examples, but these Examples are not intended to limit the present invention. ExamplesExample 1 1 Method for creating a transfer sheet The above structural formula () dye: 2 g Ethyl cellulose: 8 g Isopropanol: 90 g Total: 100 g A mixture of the above composition was mixed with a paint conditioner using glass beads for about 30 minutes,
The ink was prepared. Apply the above ink to a gravure proofing machine (plate depth 30μm)
A transfer sheet was prepared by coating capacitor paper (thickness: 10 μm) and drying it naturally. 2 How to create a recording material sheet Compound of the above structural formula () 5 g Polyester resin * 15 g Methyl ethyl ketone 80 g Total 100 g * "Vylon 200" (trade name) manufactured by Toyo Boseki Co., Ltd. The above compositions were mixed to prepare a coating solution. Apply the above coating liquid to a gravure proofing machine (plate depth 30μm)
A recording medium sheet was prepared by applying the mixture to high-quality paper and drying it naturally. 3 Transfer recording method The ink coated surface of the transfer sheet is overlapped with the coating liquid coated surface of the recording material sheet, and the transfer sheet is heated from the back side using a heat-sensitive recording head to make a clear dark orange record on the recording material. I was able to get it. In order to test the stability of the records obtained in this way, the recording surface was superimposed on high-quality paper and held at 80°C for 24 hours under a pressure of 200 g/cm 2 , but the color change of the records and the overlapping of high-quality paper There was almost no contamination by the dye. Reference Example 1 (Synthesis of dye of Example 1) 14 g of N-ethylaniline, epichlorohydrin
14.8 g, 10 ml of water, and 15 ml of ethanol were added, and the mixture was reacted and stirred on a water bath for 3 hours. After cooling, it was separated using an aqueous funnel and dried over sodium sulfate. The obtained N-ethyl-N-(2-oxy-3-
While cooling 21 g of aniline (chloropropyl) on ice,
8 ml of 50% aqueous sodium hydroxide solution was gradually added with stirring. Thereafter, after stirring for 4 hours, the produced sodium chloride was separated, and the organic layer was washed with water in a separating funnel and then dehydrated with sodium sulfate. A dye represented by the following structural formula () was obtained by coupling the obtained N-ethyl-N-glycidylaniline with a diazo solution of p-nitroaniline. mp 159-162°C Mass spectrum M + 326 λmax (chloroform) 474 nm Comparative example 1 1 Method for creating a transfer sheet A transfer sheet was created in the same manner as in Example 1. 2. Method for preparing a recording material sheet A coating solution was prepared by dissolving 15 g of polyester resin (Vylon 200) in 85 g of methyl ethyl ketone without using the compound () in Example 1, and a high-quality coating was prepared in the same manner as in Example 1. A recording medium sheet was prepared by applying the mixture to paper. 3 Transfer Recording Method The above transfer sheet and recording material sheet were superimposed and transfer recording was performed in the same manner as in Example 1 to obtain a dark yellow record. Example 1 regarding records obtained in this way
As a result of a stability test conducted in the same manner as above, the stacked high-quality paper was significantly stained orange due to migration of the dye from the recording material sheet. Furthermore, the color density of the recording material sheet was also significantly lowered due to the migration of the dye. Example 2 A dye having the structural formula shown in Table 1 was used instead of the dye shown in Example 1, and transfer recording was performed in the same manner as in Example 1, and a record with good storage stability was obtained. I was able to get it.

【表】【table】

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 支持体上に色素層を有する転写シートと、基
体上に記録層を有する被記録体シートからなる感
熱記録用シート・セツトであり、色素層がエポキ
シ基を有する色素を含有し、記録層が活性水素化
合物または有機酸無水物を含有する感熱記録用シ
ート・セツト。
1 A heat-sensitive recording sheet set consisting of a transfer sheet having a dye layer on a support and a recording sheet having a recording layer on a substrate, the dye layer containing a dye having an epoxy group, and the recording layer containing a dye having an epoxy group. A heat-sensitive recording sheet set containing active hydrogen compounds or organic acid anhydrides.
JP59117389A 1984-06-06 1984-06-07 Thermal recording sheet set Granted JPS60260391A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP59117389A JPS60260391A (en) 1984-06-07 1984-06-07 Thermal recording sheet set
US06/733,222 US4614521A (en) 1984-06-06 1985-05-10 Transfer recording method using reactive sublimable dyes
CA000481468A CA1227034A (en) 1984-06-06 1985-05-14 Transfer recording method
GB08512409A GB2159971B (en) 1984-06-06 1985-05-16 Transfer recording method
FR858507587A FR2565528B1 (en) 1984-06-06 1985-05-20 THERMAL TRANSFER PRINTING METHOD AND SET OF PRINTING SHEETS
DE19853520227 DE3520227A1 (en) 1984-06-06 1985-06-05 TRANSFER RECORDING PROCEDURE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59117389A JPS60260391A (en) 1984-06-07 1984-06-07 Thermal recording sheet set

Publications (2)

Publication Number Publication Date
JPS60260391A JPS60260391A (en) 1985-12-23
JPH0513074B2 true JPH0513074B2 (en) 1993-02-19

Family

ID=14710438

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59117389A Granted JPS60260391A (en) 1984-06-06 1984-06-07 Thermal recording sheet set

Country Status (1)

Country Link
JP (1) JPS60260391A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3788072T3 (en) * 1986-02-28 1997-02-20 Ici Plc Thermal transfer pressure.
JPH02151488A (en) * 1988-12-02 1990-06-11 Konica Corp Thermal recording material
JP4530570B2 (en) * 2001-04-09 2010-08-25 富士フイルム株式会社 Method for improving fastness of ozone gas in colored images

Also Published As

Publication number Publication date
JPS60260391A (en) 1985-12-23

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