JPS60229791A - Dye transfer body - Google Patents

Dye transfer body

Info

Publication number
JPS60229791A
JPS60229791A JP59086536A JP8653684A JPS60229791A JP S60229791 A JPS60229791 A JP S60229791A JP 59086536 A JP59086536 A JP 59086536A JP 8653684 A JP8653684 A JP 8653684A JP S60229791 A JPS60229791 A JP S60229791A
Authority
JP
Japan
Prior art keywords
color
dye transfer
formula
transfer body
dicyanovinyl
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.)
Pending
Application number
JP59086536A
Other languages
Japanese (ja)
Inventor
Nobuyoshi Taguchi
田口 信義
Akihiro Imai
章博 今井
Toshio Niwa
俊夫 丹羽
Yukichi Murata
勇吉 村田
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 Kasei Corp
Panasonic Holdings Corp
Original Assignee
Mitsubishi Kasei Corp
Matsushita Electric Industrial Co 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 Kasei Corp, Matsushita Electric Industrial Co Ltd filed Critical Mitsubishi Kasei Corp
Priority to JP59086536A priority Critical patent/JPS60229791A/en
Publication of JPS60229791A publication Critical patent/JPS60229791A/en
Pending 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
    • B41M5/3858Mixtures of dyes, at least one being a dye classifiable in one of groups B41M5/385 - B41M5/39
    • 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

Abstract

PURPOSE:To obtain a dye transfer body which is excellent in the color reproducibility with a better black image by arranging at least one kind of specified sublimating dyes to be contained in each color material layer in the dye transfer body in which three coloring material layers different in the color are arranged sequentially. CONSTITUTION:Three color inks (cyane, yellow and magenta) which at least kind of sublimating dyes selected from among naphthoquinone of formula I presenting cyane color, an anilin derivative of formula II presenting yellow color and an anilin derivative of formula III presenting magenta color (in the formulas I, II and III, X represents hydrogen atom or a methyl group and R and R' each represent 1-4C alkyl group), a high-melting-point or high-softening-point resin and a solvent are prepared. These inks are applied sequentially on the surface of a substrate made of a heat resistant high polymer film or the like to form a three-side coloring material layer.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、熱転写による記録に用いられる染料転写体に
関するものであり、とくにサーマルヘッドやレーザービ
ームなどの電子デバイスによる高速記録に利用できるも
のである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a dye transfer member used for thermal transfer recording, and is particularly applicable to high-speed recording using electronic devices such as thermal heads and laser beams.

従来例の構成とその問題点 従来、この記録方法には、安定性に優れるポリエステル
繊維の転写捺染用染料を含有する転写体が使用されてい
たが、かかる転写体は染料の昇華性が低いため着色力が
劣り、通常のサーマルヘッドの熱エネルギーでは充分な
色濃度を得ることは困難であった。又、昇華性の高いカ
ラーフォーマ−を含むイオン系染料は充分な色濃度を得
ることはできるが、保存安定性に問題があった。
Structure of the conventional example and its problems Conventionally, this recording method has used a transfer body containing a highly stable dye for transfer printing of polyester fibers, but such a transfer body has a low sublimation property of the dye. The coloring power was poor, and it was difficult to obtain sufficient color density using the thermal energy of a normal thermal head. Furthermore, although ionic dyes containing highly sublimable color formers can provide sufficient color density, they have problems with storage stability.

また、従来の転写体では、シアン、マゼンタ、イエロー
の3色の濃度特性の整合性が悪く、中間調及び飽和濃度
において十分な黒の画像が得られなかったばかりか、そ
の他の色の色再現性においてもカラー印刷と比して不十
分なものであった。
In addition, with conventional transfer materials, the consistency of the density characteristics of the three colors cyan, magenta, and yellow was poor, and not only was it not possible to obtain a sufficient black image in halftones and saturation density, but the color reproducibility of other colors was also poor. However, it was also insufficient compared to color printing.

発明の目的 本発明は、安定で昇華能力の優れているシアン、マゼン
タ、イエローの昇華性染料を用いて、黒の中間調及び十
分な飽和濃度が得られると共に、色再現性の優れたカラ
ー記録画像の得られる染料転写体を提供することを目的
とする。
Purpose of the Invention The present invention uses cyan, magenta, and yellow sublimable dyes that are stable and have excellent sublimation ability to obtain color recording with black intermediate tones and sufficient saturation density, and with excellent color reproducibility. The object of the present invention is to provide a dye transfer member from which an image can be obtained.

発明の構成 本発明は、基体上に下記一般式(1) 、 (FD、 
(110で表わされる昇華性染料からそれぞれ選ばれた
少なくとも1種類ずつを含む色相の異なる3面の色材層
を面順次に配置した染料転写体であり、黒をはじめとす
る各色の色再現性の優れた画像を提供することができる
Structure of the Invention The present invention provides the following general formula (1), (FD,
(It is a dye transfer material in which three color material layers each containing at least one type of sublimable dye represented by 110 and having different hues are sequentially arranged, and the color reproducibility of each color including black is can provide excellent images.

NHR (式中、又は水素原子又はメチル基を、R及びR′はそ
れぞれメチル基、エチル基、直鎖状もしくは分岐鎖状の
プロピル基又はブチル基を表わす)実施例の説明 前記一般式(+> 、 (IQ 、 (lで表わされる
昇華性染料の具体例としては、以下のものがあげられる
NHR (In the formula, or a hydrogen atom or a methyl group, R and R' each represent a methyl group, an ethyl group, a linear or branched propyl group, or a butyl group) Description of Examples The general formula (+ > , (IQ, (Specific examples of sublimable dyes represented by l include the following.

(1)で表わされるシアン色を呈するもの1.6−ビス
(メチルアミン)−4,8−ナフトキノン、1,6−ビ
ス(エチルアミノ)−4゜8−ナフトキノン、1,6−
ビス((fI)−プロピルアミノ)−4,8−ナフトキ
ノン、1,6−ビス((iso)−プロピルアミノ)−
4,8−ナフトキノン、1,6−ビス((→−ブチルア
ミノ)−4゜8−ナフトキノン、1,6−ビス((ig
o)−ブチルアミノ) ’、e−ナフトキノン、1−メ
チルアミノ−6−エチルアミノ−4,8−ナフトキノン
、1−メチルアミノ−6−(→−プロピルアミノー4,
8−ナフトキノン、1−メチルアミノ−5−(→−ブチ
ルアミノー4,8−ナフトキノン、1−メチルアミノ−
5−(igo)−プロピルアミノ−4,8−ナフトキノ
ン、エチルアミノ−5−(n) −プロピルアミノ−4
,8−ナフトキノン、1−エチルアミノ−6−(→−ブ
チルアミノー4,8−ナフトキノン、1−(→−プロピ
ルアミノー5−(111)−ブチルアミノ−4,8−ナ
フトキノン。
(1) exhibiting a cyan color 1.6-bis(methylamine)-4,8-naphthoquinone, 1,6-bis(ethylamino)-4°8-naphthoquinone, 1,6-
Bis((fI)-propylamino)-4,8-naphthoquinone, 1,6-bis((iso)-propylamino)-
4,8-naphthoquinone, 1,6-bis((→-butylamino)-4°8-naphthoquinone, 1,6-bis((ig
o)-butylamino)', e-naphthoquinone, 1-methylamino-6-ethylamino-4,8-naphthoquinone, 1-methylamino-6-(→-propylamino-4,
8-naphthoquinone, 1-methylamino-5-(→-butylamino-4,8-naphthoquinone, 1-methylamino-
5-(igo)-propylamino-4,8-naphthoquinone, ethylamino-5-(n)-propylamino-4
, 8-naphthoquinone, 1-ethylamino-6-(→-butylamino-4,8-naphthoquinone, 1-(→-propylamino-5-(111)-butylamino-4,8-naphthoquinone.

(■で表わされるイエロー色を呈するもの4−(2,2
−ジシアノビニル)−N、N−ジメチルアニリン、4−
(2,2−ジンアノビニル)−N、N−ジエチルアニリ
ン、4−(2,2−ジシアノビニル) −NyN ”(
→−グロピルアニリン、4−(2,2−ジシアノビニル
)−N、N−ジ(iso)−プロピルアニリン、4−(
2,2−ジシアノビニル) −N 、 N−ジ(→−ブ
チルアニリン、4−(2,2−ジシアノビニル)−N、
N−ジ(1so)−ブチルアニリン、4−(2,2−ジ
シアノビニル) −N 、 N−ジ(sea)−ブチル
アニリン、3−メチル−4−(2,2−ジシアノビニル
)−N、N−ジメチルアニリン、3−メチル−4−(2
,2−ジシアノビニル)−N、N−ジエチルアニリン、
3−メチル−4−(2,2−ジシアノビニル) −N 
、 N−ジ(→−グロビルアニリン、3−メチル−4−
(2、2−ジシアノビニル)−N。
4-(2,2
-dicyanovinyl)-N,N-dimethylaniline, 4-
(2,2-dicyanovinyl)-N,N-diethylaniline, 4-(2,2-dicyanovinyl)-NyN”(
→-Glopylaniline, 4-(2,2-dicyanovinyl)-N,N-di(iso)-propylaniline, 4-(
2,2-dicyanovinyl) -N, N-di(→-butylaniline, 4-(2,2-dicyanovinyl)-N,
N-di(1so)-butylaniline, 4-(2,2-dicyanovinyl)-N, N-di(sea)-butylaniline, 3-methyl-4-(2,2-dicyanovinyl)-N, N-dimethylaniline, 3-methyl-4-(2
,2-dicyanovinyl)-N,N-diethylaniline,
3-Methyl-4-(2,2-dicyanovinyl) -N
, N-di(→-globylaniline, 3-methyl-4-
(2,2-dicyanovinyl)-N.

N−ジ(iso)−プロピルアニリン、3−メチル−4
−(2,2−ジシアノビニル)−N、N−ジ(ロ)−ブ
チルアニリン、3−メチル−4−(2,2−ジシアノビ
ニル) −N 、 N−ジ(iso)−ブチルアニリン
、3−メチル−a−(2,2−ジシアノビニル) −N
 、 N−ジ(sec)−ブチルアニリン、4−(2、
2−ジシアノビニル)−N−エチル−N−(→−プロピ
ルアニリン、4−(2,2−ジシアノビニル)−N−エ
チル−N −(→−フチルアニリン、4−(2、2−ジ
シアノビニル) −N−メチル−N−(→−プロピルア
ニリン、4−(2,2〜ジシアノビニル)−N−メチル
−N−(→−ブチルアニリン、3−メチル−4−(2,
2−ジシアノビニル)−N−メチル−N−(n)−フロ
ヒルアニリン、3−メチル−4−(2,2−ジシアノビ
ニル)−N−メfルーN−(→−フチルアニリン、3−
メチル−4−(2,2−ジシアノビニル)−N−エチル
−N−(→−プロピルアニリン、3−メチル−4−(2
,2−ジシアノビニル)−N−エチル−N−(→−ブチ
ルアニリン、 (鴎で表わされるマゼンタ色を呈すするもの4−トリシ
アノビニル−N、N−ジメチルアニン、4−トリンアノ
ビニルーN、N−ジエチルアニリン、4−トリシアノビ
ニル−N、N −シ(→−プロヒルアニリン、4−トリ
シアノビニル−NN−ジ(i8)−プロピルアニリン、
4−トリシアノビニル−N、N−ジ(Xll)−ブチル
アニリン、4−ドリシアノビニルーN、N−ジ(i g
o)−ブチルアニリン、4−トリシアノビ= /L/ 
−N 、 N−ジ(8ec)−ブチルアニリン、3−メ
チル−4−トリシアノビニル−N、N−ジメチルアニリ
ン、4−トリシアノビニル−N−メfルーN−(→−プ
ロピルアニリン、4−トリシアノビニル−N−メチル−
N −(fl)−フチルアニリン、4−トリシアノビニ
ル−N−エチル−N−(→−プロピルアニリン、4−ト
リシアノビニル−N−エチル−N −(=)−ブチルア
ニリン、4−トリシアノビニル−N−エチル−N −(
1so) −フチルアニリン、4−トリシアノビニル−
N −エチn、−N −(sea)−ブチルアニリン、
4−ドリシアノビニルーN−(n)−プロピル−N −
(n)−ブチルアニリン、3−メチル−4−トリシアノ
ビニル−N−)fルーN−エチルアニリン。
N-di(iso)-propylaniline, 3-methyl-4
-(2,2-dicyanovinyl)-N,N-di(ro)-butylaniline, 3-methyl-4-(2,2-dicyanovinyl)-N,N-di(iso)-butylaniline, 3 -Methyl-a-(2,2-dicyanovinyl) -N
, N-di(sec)-butylaniline, 4-(2,
2-dicyanovinyl)-N-ethyl-N-(→-propylaniline, 4-(2,2-dicyanovinyl)-N-ethyl-N-(→-phthylaniline, 4-(2,2-dicyanovinyl) -N-methyl-N-(→-propylaniline, 4-(2,2-dicyanovinyl)-N-methyl-N-(→-butylaniline, 3-methyl-4-(2,
2-dicyanovinyl)-N-methyl-N-(n)-furohylaniline, 3-methyl-4-(2,2-dicyanovinyl)-N-mef-N-(→-phthylaniline, 3-
Methyl-4-(2,2-dicyanovinyl)-N-ethyl-N-(→-propylaniline, 3-methyl-4-(2
, 2-dicyanovinyl)-N-ethyl-N-(→-butylaniline, 4-tricyanovinyl-N, N-dimethylaniline, 4-tricyanovinyl-N, which exhibits a magenta color represented by a seagull) , N-diethylaniline, 4-tricyanovinyl-N,N-cy(→-prohylaniline, 4-tricyanovinyl-NN-di(i8)-propylaniline,
4-tricyanovinyl-N,N-di(Xll)-butylaniline, 4-tricyanovinyl-N,N-di(i g
o)-Butylaniline, 4-tricyanobi= /L/
-N, N-di(8ec)-butylaniline, 3-methyl-4-tricyanovinyl-N, N-dimethylaniline, 4-tricyanovinyl-N-mef-N-(→-propylaniline, 4 -Tricyanovinyl-N-methyl-
N-(fl)-phthylaniline, 4-tricyanovinyl-N-ethyl-N-(→-propylaniline, 4-tricyanovinyl-N-ethyl-N-(=)-butylaniline, 4-tricyanovinyl -N-ethyl-N-(
1so) -phthylaniline, 4-tricyanovinyl-
N-ethyn, -N-(sea)-butylaniline,
4-Dolycyanovinyl-N-(n)-propyl-N-
(n)-Butylaniline, 3-methyl-4-tricyanovinyl-N-)f-N-ethylaniline.

色材層を構成するためのインキを製造する方法としでは
、前記一般式(1)、(U)又は(I[Dで表わされる
色素を融点又は軟化点の高い樹脂と溶剤又は水等の溶媒
と非昇華性粒子とを混合してつくることができる。
As a method for producing an ink for forming a coloring material layer, a dye represented by the general formula (1), (U) or (I[D) is mixed with a resin having a high melting point or softening point and a solvent such as a solvent or water. and non-sublimable particles.

上記のインキを調製するだめの樹脂としては、通常の印
刷インキに使用されるもので良く、・ロジン系、フェノ
ール系、キシレン系、石油系、ビニル系、ポリアミド系
、アルキッド系、ニトロセルロース系、アルキルセルロ
ース、アルキルセルロース類、エチル系、エステル系な
どの油性系の樹脂あるいはマレイン酸系、アクリル酸系
、カゼイン、シェラツク、ニカワ等の水性系樹脂が使用
できるがより具体的には融点又は軟化点の高いポリカー
ボネート、ホリサルフオン、ポリフェニレンオキサイド
、ボリアリレート、セルロース誘導体等が特に有効であ
る。
The resin used to prepare the above ink may be those used in ordinary printing inks, such as rosin, phenol, xylene, petroleum, vinyl, polyamide, alkyd, nitrocellulose, Oil-based resins such as alkyl cellulose, alkyl celluloses, ethyl-based, ester-based resins, or water-based resins such as maleic acid-based, acrylic acid-based, casein, shellac, and glue can be used, but more specifically melting point or softening point Particularly effective are polycarbonate, folysulfone, polyphenylene oxide, polyarylate, cellulose derivative, etc., which have a high carbon content.

インキ調製のだめの溶剤としては、メタノール、エタノ
ール、フロパノール、ブタノールなどのア/l/ :l
−/l/ 類、メチルセロソルフ、エチルセロノルブな
どのセロソルブ類、ベンゼン、トルエン、キシレンなど
の芳香族類、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、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、ジメチルホルムアミド、塩化メチレン、クロロベ
ンゼン、りqoホルム等のハロゲン化炭化水素などが使
用できるが、水性系樹脂を使用の場合には水または水と
上記の溶剤類を混合し使用することもできる。
Solvents for ink preparation include methanol, ethanol, furopanol, butanol, etc.
-/l/, cellosolves such as methyl cellosolve and ethyl cellonorb, aromatics such as benzene, toluene and xylene, esters such as butyl acetate, acetone,
Ketones such as methyl ethyl ketone and cyclohexanone, hydrocarbons such as ligroin, cyclohexane, and kerosene, and halogenated hydrocarbons such as dimethylformamide, methylene chloride, chlorobenzene, and riqoform can be used, but when using water-based resins, It is also possible to use water or a mixture of water and the above-mentioned solvents.

本発明に用いる基体は特に限定するものではないが高分
子フィルムであれば特に有用である。例えば、ポリエチ
レンテレフタレート、ポリエチレンナフタレート、ポリ
カーボネート等のエステル系高分子、ナイロン等のアミ
ド系高分子、アセチルセルロース、セロハン等のセルロ
ース誘導体、ポリフッ化ビニリデン、4フフ化エチレン
−67)化プロピレン共重合体、テフロン等のフッ素系
高分子、ポリオキシメチレン、ポリアセタール等のエー
テル系高分子、ポリスチレン、ポリエチレン、ポリプロ
ピレン、メチルペンテンポリマー等のオレフイシ系高分
子、ポリイミド、ポリアミドイミド、ポリエーテルイミ
ド等のイミド系高分子等を用いることができる0 特に、基体がポリエステル系高分子は薄く、ある程度の
耐熱性を有しており、安価であるので有用である。
The substrate used in the present invention is not particularly limited, but polymer films are particularly useful. For example, ester polymers such as polyethylene terephthalate, polyethylene naphthalate, and polycarbonate, amide polymers such as nylon, cellulose derivatives such as acetyl cellulose and cellophane, polyvinylidene fluoride, and ethylene tetrafluoride-67) propylene copolymers. , fluorine-based polymers such as Teflon, ether-based polymers such as polyoxymethylene, polyacetal, olefinic polymers such as polystyrene, polyethylene, polypropylene, methylpentene polymers, imide-based polymers such as polyimide, polyamideimide, polyetherimide, etc. Polyester-based polymers are particularly useful because they are thin, have a certain degree of heat resistance, and are inexpensive.

又、基体がポリエステル系高分子より耐熱性のあるイミ
ド系、アミド系等の高分子は転写体を繰り返し使用する
場合、高速で使用する場合に耐熱的に優れているので有
用である。
In addition, imide-based, amide-based, and other polymers whose substrates are more heat resistant than polyester polymers are useful because they have excellent heat resistance when the transfer body is used repeatedly or at high speeds.

更に具体的な実施例を用いて説明する。This will be explained using more specific examples.

下記の第(1)、第(坤、第(3)式の構造式で表され
る染料をそれぞれ6体積部、ポリスルホン4体積部とを
塩化メチレン100体積部に溶解した。これに対して、
ジビニルベンゼン系重合体組成物、ガラスまたは鉄より
なる平均粒径8μm2粒径の標準偏差0.6μmの球形
粒子をそれぞれ別個に上記の溶液にα4体積部加えて超
音波分散し、13μm厚のポリイミドフィルムI/c3
ミルのステンレス鋼線を甘きつけたワイヤ・バーでキャ
スティングし蒐3色の染料転写体とした。
6 parts by volume of dyes represented by the following structural formulas (1), (Kon, and (3)) and 4 parts by volume of polysulfone were dissolved in 100 parts by volume of methylene chloride.On the other hand,
A divinylbenzene-based polymer composition, spherical particles made of glass or iron with an average particle size of 8 μm2 and a standard deviation of 0.6 μm, were separately added to the above solution in α4 volume parts and dispersed ultrasonically to form a polyimide with a thickness of 13 μm. Film I/c3
Three color dye transfers were made by casting milled stainless steel wire with a wire bar.

ONHC3H,(n) これらの転写体とポリエステルと無機微粒子を含むコー
ト層を有する受像体とのコート部を互いに対向させて密
着し、サーマルヘッドで染料の記録画像を描かせた。記
録条件は次のとおりである。
ONHC3H, (n) The coated portions of these transfer bodies and an image receptor having a coat layer containing polyester and inorganic fine particles were brought into close contact with each other so as to face each other, and a recorded dye image was drawn using a thermal head. The recording conditions were as follows.

主走査、副走査の線密度:4ドツト/態記録電力 :0
.7W/ドツト ヘツドの加熱時間 =8m冠 この時のシアン、マゼンタ、イエローの反射記録濃度そ
れぞれ1.6.1,4.0.9を示し、ヘッド加熱時間
を0〜5m5ec迄変イヒさせた時の濃度特性を第1図
に示す。またシアン、マゼンタ、イエローの3色の転写
体を用いて同一の受像体上に重畳させて黒の画像を記録
したところ、同じく第1図に示すような黒の濃度特性が
得られた。またこの黒の各濃度を第2図に示す色度図上
にプロットしたところ、すべてBで示す点近傍に集中し
た。又、シアン、イエロー、マゼンタ色を適宜重畳させ
て混合色を作製したところ、同じく第2図に示すような
各色の色度点が得られた。このように、本発明の化学構
造を有する染料による画像は、カラー印刷なみの黒及び
各色の色再現性と、飽和濃度と、中間調を提供すること
ができた。
Linear density of main scanning and sub-scanning: 4 dots/state Recording power: 0
.. 7W/dot head heating time = 8m crown At this time, the cyan, magenta, and yellow reflection recording densities were 1.6.1 and 4.0.9, respectively, and when the head heating time was varied from 0 to 5m5ec. The concentration characteristics are shown in FIG. Further, when a black image was recorded by using three color transfer bodies of cyan, magenta, and yellow and superimposed on the same image receptor, the same black density characteristics as shown in FIG. 1 were obtained. Furthermore, when each density of black was plotted on the chromaticity diagram shown in FIG. 2, all of the densities were concentrated near the point indicated by B. Further, when cyan, yellow, and magenta colors were appropriately superimposed to produce a mixed color, the chromaticity points of each color as shown in FIG. 2 were obtained. As described above, the image produced using the dye having the chemical structure of the present invention was able to provide black and color reproducibility of each color, saturation density, and halftone comparable to color printing.

なお、上記の実施例に用いた染料のうち第(1)式で表
わされる昇華性染料の代わりに、下記式(1)。
Note that among the dyes used in the above examples, the sublimable dye represented by the formula (1) was replaced by the following formula (1).

(4,(eeで表わされる染料を各々(1)−2体積部
、(→=2体積部、(に)=1体積部を用い、上記実施
例と同様の方法で行った結果も同様であった。
(4, (The results are also similar to those of the above example using (1) - 2 parts by volume, (→ = 2 parts by volume, and (ni) = 1 part by volume of the dye represented by ee). there were.

以下余白 (KIH7C3HN OH5C2HN 0(1)(→ (時 なお、3色の転写体を重畳させて黒を得るがわりにあら
かじめ3色の染料を混合させたインキを製造し、これを
第4の転写体としても同様の結果が得られる。
Below is the margin (KIH7C3HN OH5C2HN 0(1)(→ The same result can be obtained as well.

さらにT Is、LO841の規格に従ってこれらの染
料画像の耐日光堅牢度を試験したところ、′G〜6級の
値が得られ、十分実用に耐えられるものと判定できた。
Furthermore, when the sunlight fastness of these dye images was tested in accordance with the standard of T Is, LO841, a value of 'G~6 class was obtained, and it was determined that the dye images were sufficiently durable for practical use.

発明の効果 以上のように、本発明の染料転写体は、黒をはじめとす
る各色の色再現性及び飽和濃度、中間調においてカラー
印刷盤みの画質を得ることができると共に、耐日光等の
安定性も付与することができる。
Effects of the Invention As described above, the dye transfer material of the present invention can obtain the image quality of a color printing plate in terms of color reproducibility, saturation density, and intermediate tones of each color including black, and has excellent sunlight resistance and other properties. Stability can also be imparted.

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

第1図及び第2図は本発明の実施例における様料転写体
の特性を説明する図である。 代理人の氏名 弁理士 中 尾 敏 男 ほか1名第1
図 第2図
FIGS. 1 and 2 are diagrams illustrating the characteristics of a dye transfer body in an embodiment of the present invention. Name of agent: Patent attorney Toshio Nakao and 1 other person No. 1
Figure 2

Claims (1)

【特許請求の範囲】[Claims] (1)基体上に下記一般式(1) 、 (IQ 、 (
IIDで表わされる昇華性染料からそれぞれ選ばれた少
なくとも1種類ずつを含む色相の異なる3面の色材層を
面順次に配置した染料転写体。 (式中、Xは水素原子又はメチル基を、R及びR′はそ
れぞれメチル基、エチル基、直鎖状もしくは分岐鎖状の
プロピル基又はブチル基を表わす)(躊 一般式(+)
、(II)又は(坤のうち、置換基の異なる2種以上の
昇華性染料で1色の色材層を構成した特許請求の範囲第
1項記載の染料転写体。 (1一般式(1) 、 (II) t (llf)から
それぞれ選ばれた少なくとも1種類ずつの昇華性染料を
含む3面の前記色材層と、一般式(1) 、 (11)
 、 (曲のそれぞれから少なくとも1種類ずつ選ばれ
てなる第4の前記色材層を面順次に配置したことを特徴
とする特許請求の範囲第1項又は第2項記載の染料転写
体。
(1) The following general formula (1), (IQ, (
A dye transfer body in which three coloring material layers each containing at least one kind selected from sublimable dyes represented by IID and having different hues are sequentially arranged. (In the formula, X represents a hydrogen atom or a methyl group, R and R' each represent a methyl group, an ethyl group, a linear or branched propyl group, or a butyl group)
, (II) or (Kon), the dye transfer material according to claim 1, wherein one color material layer is composed of two or more sublimable dyes having different substituents. ), (II) t (llf), and the coloring material layers on three sides each containing at least one sublimable dye selected from t (llf), and the general formulas (1) and (11).
, (The dye transfer material according to claim 1 or 2, characterized in that the fourth coloring material layer selected from at least one type from each of the songs is arranged in a plane-sequential manner.
JP59086536A 1984-04-27 1984-04-27 Dye transfer body Pending JPS60229791A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59086536A JPS60229791A (en) 1984-04-27 1984-04-27 Dye transfer body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59086536A JPS60229791A (en) 1984-04-27 1984-04-27 Dye transfer body

Publications (1)

Publication Number Publication Date
JPS60229791A true JPS60229791A (en) 1985-11-15

Family

ID=13889717

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59086536A Pending JPS60229791A (en) 1984-04-27 1984-04-27 Dye transfer body

Country Status (1)

Country Link
JP (1) JPS60229791A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0163145A2 (en) * 1984-04-27 1985-12-04 Matsushita Electric Industrial Co., Ltd. Dye transfer type thermal printing sheets and method for printing
JPS62196186A (en) * 1985-12-24 1987-08-29 イ−ストマン コダック カンパニ− Yellow dyestuff dative element used for heat dyestuff transfer
WO1987006533A1 (en) * 1986-04-30 1987-11-05 Dai Nippon Insatsu Kabushiki Kaisha Thermal transfer sheet for forming color image
JPS63170092A (en) * 1987-01-08 1988-07-13 Hitachi Ltd Thermal transfer sheet
EP0279467A2 (en) * 1987-02-20 1988-08-24 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer sheet
US4898909A (en) * 1987-01-07 1990-02-06 Basf Aktiengesellschaft Aqueous polyacrylate dispersions and their use for the production of self-adhesive structures having good low temperature adhesion
US4999026A (en) * 1986-09-05 1991-03-12 Basf Aktiengesellschaft Transferring dyes for thermal printing: tri-cyano-vinyl aniline dyes
EP0701907A1 (en) 1994-09-13 1996-03-20 Agfa-Gevaert N.V. A dye donor element for use in a thermal dye transfer process
EP0733487A2 (en) 1995-01-30 1996-09-25 Agfa-Gevaert N.V. Method for making a lithographic printing plate requiring no wet processing
EP0792757A1 (en) 1996-02-27 1997-09-03 Agfa-Gevaert N.V. Dye donor element for use in thermal transfer printing

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0163145A2 (en) * 1984-04-27 1985-12-04 Matsushita Electric Industrial Co., Ltd. Dye transfer type thermal printing sheets and method for printing
US4777159A (en) * 1984-04-27 1988-10-11 Matsushita Electric Industrial Co., Ltd. Dye transfer type thermal printing sheets and method for printing
JPS62196186A (en) * 1985-12-24 1987-08-29 イ−ストマン コダック カンパニ− Yellow dyestuff dative element used for heat dyestuff transfer
WO1987006533A1 (en) * 1986-04-30 1987-11-05 Dai Nippon Insatsu Kabushiki Kaisha Thermal transfer sheet for forming color image
US4999026A (en) * 1986-09-05 1991-03-12 Basf Aktiengesellschaft Transferring dyes for thermal printing: tri-cyano-vinyl aniline dyes
US4898909A (en) * 1987-01-07 1990-02-06 Basf Aktiengesellschaft Aqueous polyacrylate dispersions and their use for the production of self-adhesive structures having good low temperature adhesion
JPS63170092A (en) * 1987-01-08 1988-07-13 Hitachi Ltd Thermal transfer sheet
EP0279467A2 (en) * 1987-02-20 1988-08-24 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer sheet
EP0701907A1 (en) 1994-09-13 1996-03-20 Agfa-Gevaert N.V. A dye donor element for use in a thermal dye transfer process
EP0733487A2 (en) 1995-01-30 1996-09-25 Agfa-Gevaert N.V. Method for making a lithographic printing plate requiring no wet processing
EP0792757A1 (en) 1996-02-27 1997-09-03 Agfa-Gevaert N.V. Dye donor element for use in thermal transfer printing

Similar Documents

Publication Publication Date Title
JPS60229791A (en) Dye transfer body
JPH05237B2 (en)
JPS5978894A (en) Coloring matter for heat-sensitive transfer recording
JPS60229793A (en) Dye transfer body
JPH07137455A (en) Image forming method by thermal transfer
JPS60229789A (en) Dye transfer body
JPH0532233B2 (en)
JPS5993389A (en) Thermal transfer color sheet
JPS59227493A (en) Transfer sheet
JPH0513077B2 (en)
JPS5993391A (en) Thermal transfer color sheet
JPH0535079B2 (en)
US4973573A (en) Thermal transfer dye-providing material
JPH0533159B2 (en)
JPH02130190A (en) Thermal transfer dye donating material
JPS60229786A (en) Heat transfer thermal recording
JPH04112089A (en) Thermal transfer material
JPH0533679B2 (en)
JP3353530B2 (en) Transfer sheet
JPH02265791A (en) Thermal transfer recording material
JPS61255897A (en) Coloring matter for recording
JPH106657A (en) Thermosensitive transfer sheet
JP3406350B2 (en) Thermal transfer sheet
JPH0688462B2 (en) Dye for thermal transfer recording
JPH02588A (en) Dye transfer