JPH022077A - Dye transfer material and preparation thereof - Google Patents

Dye transfer material and preparation thereof

Info

Publication number
JPH022077A
JPH022077A JP63144242A JP14424288A JPH022077A JP H022077 A JPH022077 A JP H022077A JP 63144242 A JP63144242 A JP 63144242A JP 14424288 A JP14424288 A JP 14424288A JP H022077 A JPH022077 A JP H022077A
Authority
JP
Japan
Prior art keywords
dye
layer
water
recording
concentration
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.)
Granted
Application number
JP63144242A
Other languages
Japanese (ja)
Other versions
JP2502683B2 (en
Inventor
Tetsuji Kawakami
哲司 川上
Hiromu Matsuda
宏夢 松田
Keiichi Yubagami
弓場上 惠一
Akihiro Imai
章博 今井
Nobuyoshi Taguchi
田口 信義
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.)
Panasonic Holdings Corp
Original Assignee
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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP63144242A priority Critical patent/JP2502683B2/en
Priority to EP89302175A priority patent/EP0331525B1/en
Priority to US07/318,588 priority patent/US5137865A/en
Priority to CA000592655A priority patent/CA1327123C/en
Priority to DE68918883T priority patent/DE68918883T2/en
Publication of JPH022077A publication Critical patent/JPH022077A/en
Priority to US07/905,990 priority patent/US5334574A/en
Application granted granted Critical
Publication of JP2502683B2 publication Critical patent/JP2502683B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Thermal Transfer Or Thermal Recording In General (AREA)

Abstract

PURPOSE:To use a dye having high weatherability and low sublimability and to hold high saturated recording density over many times by successively laminating a high concn. dye layer and a dye permeable low concn. layer containing a water-soluble or water-dispersible resin to a substrate to form a color material layer. CONSTITUTION:In a transfer material 1, a high concn. dye layer 9 containing a dye, a dye permeable low concn. layer 10 containing the dye at concn. lower than that of the high concn. layer and containing a water-soluble or water-dispersible resin and a lubricating layer 11 containing a lubricant are successively laminated to a transfer substrate 2 to form a color material layer 3. By performing recording by closely bringing the color material layer 3 of this dye transfer material 1 into contact with the dyeing layer of an image receiving material having dyeability, many-time recording reduced in the lowering of initial recording density becomes possible. Since the lubricating layer 11 is provided, the dye transfer material or image receiving material is selectively heated from the rear thereof in such a state that the running speed of the dye transfer material to a thermal recording head is lower than that of the image receiving material to transfer the dye in the color material layer to the dyeing layer and an image is formed on the image receiving material. Even at the time of many-time recording, the lowering of initial recording density can be reduced.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、染料転写体上の色素を受像体上の染若居へ転
写し画像を形成する染料転写型感熱記録において、染料
転写体の同一カ所を複数回使用する多数回記録のための
染料転写体及びその製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a dye transfer type thermal recording in which an image is formed by transferring the dye on a dye transfer member to a dye layer on an image receptor. The present invention relates to a dye transfer member for multiple recording using multiple times, and a method for manufacturing the same.

従来の技術 昇華性の高い色素を用いた染料転写型感熱記録は記録ド
ツト毎の濃度階調記録が可能なフルカラー記録方式であ
るが、転写体コストが高い欠点があり転写体の多数回利
用に対する試みが行われている。多数回記録の報告とし
て、 (1)「昇華転写型感熱記録体のn倍モード記録持性」
 (昭和60年第2回ノンインパクトプリンティング技
術シンポジウム論文集、Plot−104)及び(2)
「多数回記録用昇華型フィルムの検討」 (画像電子学
会昭和61年度全国大会予稿集)がある。
Conventional technology Dye transfer type thermal recording using dyes with high sublimation property is a full-color recording method that can record density gradations for each recorded dot, but it has the drawback of high cost for the transfer body, making it difficult to use the transfer body multiple times. Attempts are being made. As a report on multiple recordings, (1) "Nx mode recording durability of sublimation transfer type thermal recording material"
(Proceedings of the 2nd Non-Impact Printing Technology Symposium in 1985, Plot-104) and (2)
``Study of sublimation film for multiple recording'' (Proceedings of the 1986 National Conference of the Institute of Image Electronics Engineers).

(1)(2)は共に相対速度方式による多数回記録特性
に関する。
(1) and (2) both relate to multiple recording characteristics using the relative speed method.

多数回記録には同一部分をN回繰り返し使用する単純繰
り返し方式と、受像体に対し染料転写体の供給速度を1
/nにし実質的にn回の多数回記録を行うn倍モード相
対速度方式の2つがある。
For multiple recordings, there is a simple repeat method in which the same area is repeatedly used N times, and a method in which the dye transfer material is supplied to the image receptor at a rate of 1
There are two types: an n-times mode relative speed method in which recording is performed virtually n times at n times.

相対速度方式は、染料転写体・受像体間の滑性化のため
の工夫が必要だが、常に転写体の未記録部分が供給され
るため実質的な繰り返し数は単純繰り返し方式に比べ大
きくとることができる。
The relative speed method requires some effort to create smoothness between the dye transfer member and the image receiver, but since the unrecorded portion of the transfer member is always supplied, the actual number of repetitions must be larger than that of the simple repetition method. I can do it.

(+)では転写体・受像体間に球形スペーサ粒子を介し
、繰り返し数n=12で記録濃度的1.8を実現してい
る。(2)では転写体と受像体を密着走行。
In (+), spherical spacer particles are interposed between the transfer member and the image receiver, and a recording density of 1.8 is achieved with the number of repetitions n=12. In (2), the transfer body and image receptor are run closely together.

させn=10で記録濃度的1.0を実現している。When n=10, a recording density of 1.0 is achieved.

発明が解決しようとする課題 通常記録(1回記録)と同等のフルカラー画像記録を実
現するには、通常記録時の飽和記録1度度と同等の飽和
記録1度(約1.5〜1.8)を確保することと、記録
履歴の影響がでないよう同一記録エネルギーに対し繰り
返し回数による記878度変化が小さいことが条件とな
る。
Problems to be Solved by the Invention In order to achieve full-color image recording equivalent to normal recording (one-time recording), it is necessary to perform 1 degree of saturated recording (approximately 1.5 to 1.5 degrees), which is equivalent to 1 degree of saturated recording during normal recording. 8) and that the change in 878 degrees due to the number of repetitions for the same recording energy be small so as not to be influenced by the recording history.

従来例(1)では、多数回記録に必要な色素量を充分に
確保すれば、記録特性的には前記条件を満足している。
Conventional Example (1) satisfies the above conditions in terms of recording characteristics if a sufficient amount of dye necessary for multiple recordings is ensured.

しかし染料転写体・受像体間に相対速度走行を可能にす
る滑性を与えると同時に、転写量を昇華過程により律速
させるためのスペースを設けるため、使用可能な色素が
昇華性の高い色素に限られる。従来例(2)では密着拡
散転写により昇華性の低い高耐候性色素を使用すること
が可能であるが、多数回記録に必要な色素量を十分確保
しても、同一記録エネルギーに対する繰り返し回数増加
による記録濃度低下が大きく、またその結果多数回記録
時に得られる飽和記録濃度が実用レベルに達していない
However, in order to provide lubricity between the dye transfer member and receiver to enable relative speed running, and at the same time provide space to control the amount of transfer through the sublimation process, the usable dyes are limited to dyes with high sublimability. It will be done. In conventional example (2), it is possible to use highly weather-resistant dyes with low sublimation properties through contact diffusion transfer, but even if sufficient amount of dye is secured for multiple recordings, the number of repetitions for the same recording energy increases. As a result, the saturation recording density obtained during multiple recordings has not reached a practical level.

これに対して、少なくとも昇華性の高い色素と結着剤を
含み、層表面側における前記色素の重量濃度が層基体側
より低いよう構成された色材層を基体上に有する染料転
写体を用いることにより、密着拡散転写において染料転
写体の同一カ所を多数回使用することが可能になる。し
かしながら、油溶性樹脂を含む色素低濃度層を有機溶剤
溶液塗布によって積層すると、予め塗布しである色素高
濃度層が溶解してしまい色材層表面の色素濃度を低く抑
えることが難しく、本来予期できる良好な多数回記録特
性が得られなかった。
In contrast, a dye transfer material is used which has a coloring material layer on a substrate that contains at least a highly sublimable dye and a binder, and is configured such that the weight concentration of the dye on the layer surface side is lower than on the layer base side. This makes it possible to use the same location on the dye transfer member many times in contact diffusion transfer. However, when a low dye concentration layer containing an oil-soluble resin is laminated by coating with an organic solvent solution, the pre-coated high dye concentration layer dissolves, making it difficult to keep the dye concentration on the surface of the colorant layer low, which was originally expected. Good multi-time recording characteristics could not be obtained.

本発明は、前記問題点を解決し、実用性の高い高耐候性
低昇華性の色素が使用可能で、同一記録エネルギーに対
する記録回数増に伴う記録濃度低下が小さく、より多数
回まで高い飽和記録濃度を保持することができ、より低
いランニングコストで通常の1回記録と同等のフルカラ
ー記録を可能とする多数回記録用染料転写体を提供する
ことを目的とする。
The present invention solves the above problems, allows the use of highly practical dyes with high weather resistance and low sublimation, reduces the decrease in recording density as the number of recordings increases for the same recording energy, and allows high saturation recording even for a greater number of recordings. It is an object of the present invention to provide a dye transfer member for multiple recordings, which can maintain density and enable full-color recording equivalent to normal one-time recording at lower running costs.

課題を解決するための手段 少なくとも色素を含む色素高濃度層と、層中の色素濃度
が前記高濃度層より低く、少なくとも水溶性樹脂または
水分散性樹脂を含む色素透過性低濃度層とを、基体上に
順次積層した構成とする。
Means for Solving the Problems A dye high concentration layer containing at least a dye, and a dye permeable low concentration layer having a dye concentration lower than the high concentration layer and containing at least a water-soluble resin or a water-dispersible resin, The structure is such that they are sequentially laminated on a base.

作用 染料転写体、受像体間にスペースを設けない場合、色素
の転写は色材層・染着層間の色素の拡散現象に支配され
る。従って、多数回記録の色素消費過程における色材層
表面の色素濃度変化に着目すると、通常の形成法による
色材層では初期状態において色材層内部に色素の濃度勾
配が無いため、初回の記録時には表面付近の色素が消費
され、色材層表面の色素濃度は色材層内部の1度の半分
近くに低下する。2回目以降は色材層内部の濃度勾配に
より内部からも色素が供給されるため色材層表面の色素
濃度低下速度は非常に小さくなる。従って同一記録エネ
ルギーを加えたときの多数回記録時の記録濃度変化は、
初回から2回目にかけて大きく低下し、以降の記録濃度
低下は小さい。そこで、まず基体上に色素高濃度層を設
け、次に色素の重量濃度が低い届を水溶性樹脂または水
分散性樹脂を含む水系塗液で塗布することにより、先に
塗布した色素高濃度層を溶解することなく色材層表面側
の色素重量濃度を低くし色材層内部に濃度勾配を持たせ
ることで、初回から色材層内部からの色素供給がなされ
ることになり、この結果、色材層表面の色素濃度の急激
な低下に伴う、初期の記録濃度の急激な低下を大きく改
善することができる。
Function: When no space is provided between the dye transfer member and the image receiver, the transfer of the dye is dominated by the diffusion phenomenon of the dye between the coloring material layer and the dyeing layer. Therefore, if we focus on the change in dye concentration on the surface of the coloring material layer during the dye consumption process of multiple recordings, we can see that in the coloring material layer formed by the normal method, there is no gradient of dye concentration inside the coloring material layer in the initial state. Sometimes, the dye near the surface is consumed, and the dye concentration on the surface of the coloring material layer decreases to nearly half of the concentration inside the coloring material layer. From the second time onwards, the dye is supplied from inside due to the concentration gradient inside the coloring material layer, so the rate of decrease in the dye concentration on the surface of the coloring material layer becomes very small. Therefore, the change in recording density during multiple recordings when the same recording energy is applied is:
The recording density decreases greatly from the first time to the second time, and the subsequent decrease in recording density is small. Therefore, by first providing a high dye concentration layer on the substrate and then coating a layer with a low weight concentration of the dye with a water-based coating solution containing a water-soluble resin or a water-dispersible resin, it is possible to coat the layer with a high dye concentration that was previously applied. By lowering the dye weight concentration on the surface side of the coloring material layer without dissolving it and creating a concentration gradient inside the coloring material layer, the dye is supplied from inside the coloring material layer from the beginning, and as a result, It is possible to greatly improve the rapid decrease in the initial recording density caused by the rapid decrease in the dye concentration on the surface of the coloring material layer.

実施例 本発明について具体的に説明する。Example The present invention will be specifically explained.

良好、な多数回記録特性が得られる、少なくとも昇華性
の高い色素と結着剤を含み、層表面側における前記色素
の重量濃度が周基体側より低いよう構成された色材層を
基体上に存する染料転写体において、具体的に前記色素
濃度分布を実現するための色材層形成方法としては、 (1)相異なる色素重量濃度を有する複数の層を、濃度
の高い方から基体上に順次積層することにより色材層を
形成する方法と、 (2)基体上に少なくとも色素と結着剤とからなる色材
層を設けた後、色材層表面近傍の色素を除去することに
より色材層を形成する方法 とがある。
A coloring material layer that provides good multi-time recording characteristics, contains at least a highly sublimable dye and a binder, and is configured such that the weight concentration of the dye on the surface side of the layer is lower than on the surrounding substrate side. In existing dye transfer materials, the method of forming a coloring material layer to specifically realize the above-mentioned dye concentration distribution is as follows: (1) A plurality of layers having different dye weight concentrations are sequentially formed on a substrate from the one with the highest concentration. (2) A method of forming a coloring material layer by laminating layers; There is a method of forming layers.

(2)については、所望の色素濃度分布を安定に且つ厳
密に得ることは難しいので、通常(1)の方法によって
形成されると考えられる。
Regarding (2), since it is difficult to stably and precisely obtain the desired dye concentration distribution, it is considered that the method (1) is usually used.

(1)においては、数層を重ね色材層内部全体に濃度勾
配をつけることが好ましいが、製造の最も容易な2層構
成即ち、少なくとも色素を含む色素高濃度層と、層中の
色素重量濃度が前記高濃度層より低い色素透過性低濃度
層とを、基体上に順次積層して色材層とした染料転写体
においても、多数回記録時の初期記録濃度変化を大きく
改善することが十分可能である。2層構成において、初
期の記録濃度変化を抑えるには、色素透過性低濃度層の
色素型ffi濃度を色素高濃度層の色素重量濃度の1/
2.以下とすることがより好ましく効果が大きい。色素
透過性低濃度層の厚みは、色素透過性低濃度層の色素濃
度の色素高濃度層の色素濃度に対する比率により最も効
果の高い厚みに調整することが出来る。比率が高い場合
は厚く、低い場合には薄くすることで調整可能であり、
色素透過性低濃度層の色素濃度が零に近い場合は1μm
以下にすることが好ましい。また、2層構成においては
、色素透過性低濃度層に長期保存時の色素高濃度層の保
護機能を持たせることが出来るため、従来保存性の観点
で問題のあった色素高濃度層の色素含有率を50重量%
以上にすることが可能であり、これにより多量の色素を
効率よく染料転写体上に保持することができ、また高?
農度で色素を保持するため、より多数回の記録まで色材
層内部の色素濃度を高く保てるため、より多数回の記録
まで記録濃度変化の少ない高濃度記録が出来る。しかし
、色素濃度が異なる同じ様な溶剤組成の塗液を繰り返し
塗布する方法では、後から塗布する塗液によって先に設
けた色素高濃度層が溶解してしまい、その高濃度の色素
のために容易に後から塗布している色素透過性低濃度層
の色素濃度を高めてしまう。このため良好な多数回記録
特性を得ることができなかった。
In (1), it is preferable to stack several layers and create a concentration gradient throughout the interior of the coloring material layer, but the easiest two-layer structure to manufacture is a layer with a high dye concentration containing at least a dye, and a layer with a high dye concentration containing at least a dye. Even in a dye transfer body in which a dye-permeable low-density layer whose density is lower than that of the high-density layer is sequentially laminated on a substrate as a coloring material layer, it is possible to greatly improve the initial recording density change during multiple recordings. It is quite possible. In a two-layer configuration, in order to suppress initial recording density changes, the dye-type ffi density of the dye-transmissive low-density layer should be set to 1/1 of the dye weight density of the dye-high density layer.
2. It is more preferable to set it to the following, and the effect is large. The thickness of the dye-permeable low-density layer can be adjusted to the most effective thickness by adjusting the ratio of the dye concentration of the dye-permeable low-density layer to the dye concentration of the dye-high concentration layer. It can be adjusted by making it thicker when the ratio is high and thinner when it is low.
1μm if the dye concentration of the dye permeability low density layer is close to zero
It is preferable to do the following. In addition, in the two-layer structure, the dye-permeable low-density layer can have a protective function for the high-dye concentration layer during long-term storage. Content rate: 50% by weight
This allows a large amount of dye to be efficiently retained on the dye transfer body, and also allows for high dye transfer.
Since the dye is retained at a constant rate, the dye concentration inside the coloring material layer can be maintained high even after many more recordings, so high-density recording with little change in recording density can be achieved even after many more recordings. However, in the method of repeatedly applying coating liquids with the same solvent composition with different pigment concentrations, the coating liquid applied later dissolves the previously formed high pigment concentration layer, and the high concentration of pigment This will easily increase the dye concentration of the dye-permeable low-density layer coated later. For this reason, it was not possible to obtain good multiple recording characteristics.

そこで「少なくとも色素を含む色素高濃度層と、層中の
色素濃度が前記高濃度層より低く、少なくとも水溶性樹
脂または水分散性樹脂を含む色素透過性低濃度層とを、
基体上に順次積層」することで染料転写体を形成すると
、色素透過性低濃度層は色素高濃度層を溶解しない水系
塗液として塗布するので上記に述べたような問題点は解
決できる。
Therefore, ``a dye high concentration layer containing at least a dye, and a dye permeable low concentration layer in which the dye concentration in the layer is lower than the high concentration layer and containing at least a water-soluble resin or a water-dispersible resin,
When a dye transfer body is formed by sequentially laminating dye transfer materials on a substrate, the above-mentioned problems can be solved because the dye-permeable low-concentration layer is applied as an aqueous coating solution that does not dissolve the dye-high concentration layer.

第1図に構成例を示す。転写体1は、転写基体2上に色
素高濃度層9、色素透過性低濃度層10を順次・積層し
色材層3としたものである。また、受像体4は、受像基
体5上に染着層6を設けたものである。
FIG. 1 shows an example of the configuration. The transfer body 1 is made by sequentially laminating a dye high concentration layer 9 and a dye transmitting low concentration layer 10 on a transfer substrate 2 to form a coloring material layer 3. Further, the image receptor 4 has a dyeing layer 6 provided on an image receiving substrate 5.

また、染料転写体の熱記録ヘッドの対する走行速度が受
像体の熱記録ヘッドに対する走行速度より小さな状態で
、染料転写体裏面もしくは受像体裏面より選択的に加熱
して色材層中の色素を受像体染着層へ転写し受像体上へ
画像を形成する相対速度記録方式の多数回記録において
も、相対速度比nの増加による記録濃度低下を抑えるこ
とが可能である。
In addition, when the running speed of the dye transfer member with respect to the thermal recording head is smaller than the running speed of the image receiver with respect to the thermal recording head, the dye in the color material layer is heated selectively from the back surface of the dye transfer member or the back surface of the image receiver. Even in multiple recordings using a relative speed recording method in which an image is transferred to the dyed layer of the image receptor and formed on the image receptor, it is possible to suppress a decrease in recording density due to an increase in the relative speed ratio n.

ここで相対速度記録方式の原理を第2図に示す。The principle of the relative speed recording method is shown in FIG. 2.

転写体1と受像体4は色材層染着層が密着するようにプ
ラテン7によりサーマルヘッド8に押圧される。受像体
4のサーマルヘッド8に対する速度Vに対し、転写体1
はv/n(n=1、・2、拳・)で走行する。転写体の
走行方向は、受像体の走行方向に対し同方向でも逆方向
でも構わない。しかしながら、転写体がサーマルヘッド
によって加熱されているので転写体色材層と受像体染着
層の融資が起こり易く、少なくとも色材層もしくは染着
層の一方に十分な滑性が必要である。
The transfer body 1 and the image receptor 4 are pressed against a thermal head 8 by a platen 7 so that the dyed coloring layers are brought into close contact with each other. With respect to the speed V of the image receptor 4 with respect to the thermal head 8, the transfer body 1
runs at v/n (n=1, ・2, fist・). The traveling direction of the transfer body may be the same as or opposite to the traveling direction of the image receptor. However, since the transfer body is heated by a thermal head, the color material layer of the transfer body and the dyed layer of the image receptor tend to collide, and at least one of the color material layer and the dyed layer must have sufficient lubricity.

そこで、 「少なくとも色素を含む色素高濃度層と、層
中の色素濃度が前記高濃度層より低く、少なくとも水溶
性樹脂または水分散性樹脂と滑剤を含む色素透過性低濃
度層とを、基体上に順次積層して色・材層とした」染料
転写体及び「少なくとも色素を含む色素高濃度層と、層
中の色素濃度が前記高濃度層より低く、少なくとも水溶
性樹脂または水分散性樹脂を含む色素透過性低濃度層と
、少なくとも滑剤を含む滑剤層とを、基体上に順次積層
して色材層とした」染料転写体について説明す前記°2
Nの染料転写体は相対速度記録を可能にする滑性を付与
した染料転写体である。このような色材層表面に滑性を
有する染料転写体の具体的な表面状態を形成する方法と
しては、 (1)色素高濃度層を塗布して形成した後、水溶性樹脂
または水分散性樹脂と滑剤を含む水系塗液を塗布するこ
とで滑性を付与した色素透過性低濃度層を形成する方法
と、 (2)前記のような方法で、予め適当な色素濃度分布が
形成された唐土に少なくとも滑剤を含む滑剤層を積層す
る方法、 とがある。
Therefore, "a high dye concentration layer containing at least a dye and a dye permeable low concentration layer having a dye concentration lower than that of the high concentration layer and containing at least a water-soluble resin or a water-dispersible resin and a lubricant, are formed on a substrate." A dye transfer body that is sequentially laminated to form a color/material layer, and a dye transfer body containing at least a dye with a high dye concentration layer, the dye concentration in the layer being lower than the high concentration layer and containing at least a water-soluble resin or a water-dispersible resin. A dye-transmissive low-density layer containing a dye and a lubricant layer containing at least a lubricant are sequentially laminated on a substrate to form a coloring material layer.''
The N dye transfer material is a dye transfer material provided with lubricity that enables relative speed recording. As a method for forming a specific surface condition of a dye transfer material having lubricity on the surface of the color material layer, (1) After coating and forming a dye high concentration layer, a water-soluble resin or a water-dispersible resin is applied. (2) A method in which a dye-permeable low-density layer is formed with lubricity by applying a water-based coating solution containing a resin and a lubricant, and (2) an appropriate dye concentration distribution is formed in advance by the method described above. There is a method of laminating a lubricant layer containing at least a lubricant on clay.

第3図に(2)の構成例を示す((1)については、第
1図と同様である)。転写体1は、転写基体2上に色素
高濃度層9、色素透過性低濃度層10、滑剤層11を順
次積層し色材層3としたものである。
FIG. 3 shows a configuration example of (2) ((1) is the same as in FIG. 1). The transfer body 1 has a dye layer 3 formed by sequentially laminating a dye high concentration layer 9, a dye permeable low concentration layer 10, and a lubricant layer 11 on a transfer substrate 2.

本染料転写体を使用し、染料転写体の色材層と色素染着
性を何する受像体の染着層とを密着し多数回記録を行う
ことにより、初期記録143度低下の小さい多数回記録
が可能であ゛る。また本染料転写体の色材層て十分な滑
性を付与する滑剤を表面に含んでいるものは、染料転写
体の熱記録ヘッドに対する走行速度が前記受像体の熱記
録ヘッドに対する走行速度より小さな状態で、染料転写
体裏面もしくは受像体裏面より選択的に加熱して色材層
中の色素を染着層へ転写し受像体上へ画像を形成する相
対速度記録方式の多数回記録においても、初期記録濃度
低下の小さい多数回記録が可能である。
By using this dye transfer material and performing multiple recordings with the color material layer of the dye transfer material and the dyed layer of the image receptor, which determines the dye dyeing property, being brought into close contact, it is possible to perform multiple recordings with a small decrease of 143 degrees in the initial recording. Recording is possible. In addition, if the coloring material layer of the present dye transfer body contains a lubricant on the surface that imparts sufficient lubricity, the traveling speed of the dye transfer body relative to the thermal recording head is smaller than the traveling speed of the image receptor relative to the thermal recording head. Even in multiple recordings using the relative speed recording method, in which the dye in the color material layer is transferred to the dyed layer by selectively heating the back surface of the dye transfer member or the back surface of the image receptor to form an image on the image receptor. It is possible to perform multiple recordings with a small decrease in initial recording density.

以下本発明に用いる具体的材料について説明を加える。Specific materials used in the present invention will be explained below.

色素としては分散色素、塩基性染料及び塩基性染4−1
のグイフォーマなどがある。
As pigments, disperse pigments, basic dyes, and basic dyes 4-1
There are such things as Guiforma.

転写に必要な加熱源は、サーマルヘッド、通電方式、レ
ーザによるヒートモード加熱等特に限定されず、従って
染料転写体、受像体に使用する基体も用途により種々の
ものが使用可能である。例えばサーマルヘッドに対する
染料転写体の基体としては、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
イミド、ポリアミドイミド、ポリエーテルイミド等のイ
ミド系高分子等があり、基体の熱記録ヘッドに直接接す
る面には必要に応じて耐熱層或は滑性層を設ける。また
通電記録、誘導加熱記録を行うためには、上記材料等に
導電性を付与したフィルムが使用される。
The heat source necessary for transfer is not particularly limited, such as a thermal head, an energization method, heat mode heating using a laser, etc. Therefore, various substrates can be used for the dye transfer member and image receiver depending on the purpose. For example, as a substrate for a dye transfer material for a thermal head, ester polymers such as polyethylene terephthalate, polyethylene naphthalate, and polycarbonate, amide polymers such as nylon, cellulose derivatives such as acetylcellulose and cellophane, polyimide, polyamideimide, polyamide, etc. Examples include imide-based polymers such as etherimide, and a heat-resistant layer or a slippery layer is provided on the surface of the substrate that comes into direct contact with the thermal recording head, if necessary. Further, in order to perform current recording and induction heating recording, a film made of the above-mentioned materials or the like is used to impart conductivity.

色素高濃度層を形成する結着樹脂は特に限定するもので
はないが、ポリエステル樹脂、ブチラール樹脂、ナイロ
ン樹脂、ポリカーボネート樹脂、ウレダン樹脂、塩素化
ポリエチレン、塩素化ポリプロピレン、 (メタ)アク
リル樹脂、ポリスチレン樹脂、AS樹脂、ポリスルホン
樹脂、ポリフェニレンオキシド、セルロース誘導体、等
を挙げることができ、必要な特性に応じて選択、組み合
わさて用いられる。
The binder resin that forms the high dye concentration layer is not particularly limited, but examples include polyester resin, butyral resin, nylon resin, polycarbonate resin, urethane resin, chlorinated polyethylene, chlorinated polypropylene, (meth)acrylic resin, and polystyrene resin. , AS resin, polysulfone resin, polyphenylene oxide, cellulose derivative, etc., which are selected and used in combination depending on the required characteristics.

色素高濃度層は、少なくとも色素を含んでいれば良いが
、前記のような結着材の他、滑剤、色素分散剤など各種
添加剤を含んでいても良い。しかしシリコーン化合物Φ
ワックスなどを添加して色素高濃度層の表面自由エネル
ギーを小さくしてしまうと、表面自由エネルギーが比較
的高い水系塗液は塗布が困難になるので注意が必要であ
る。
The high dye concentration layer only needs to contain at least a dye, but may also contain various additives such as a lubricant and a dye dispersant in addition to the binder described above. However, silicone compounds Φ
Care must be taken because if the surface free energy of the dye-rich layer is reduced by adding wax or the like, it will be difficult to apply an aqueous coating liquid with a relatively high surface free energy.

色素高濃度層を形成するためのインク調製にしようする
溶剤としては、メタノール、エタノール、プロパツール
、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、キシレンなどの芳香族類、酢酸ブチルなどのエス
テル類、アセトン、2−ブタノン、シクロヘキサノンな
どのケトン類、N、  N−ジメチルホルムアミドなど
の窒素化合物類、ジクロルメタン、クロルベンゼン、ク
ロロホルムなどのハロゲン化炭化水素などが使用できる
。更に、インクを基材上に塗布する方法としては、リバ
ースロールコータ−グラビアコーター ロッドコーター
 エアドクタコーターなどを使用して実施することがで
きる(原崎勇次著、横書店1979年発行「コーティン
グ方式」)。
Solvents used in the preparation of ink to form a high dye concentration layer include alcohols such as methanol, ethanol, propatool, butanol, methyl cellosolve,
Cellosolves such as ethyl cellosolve, aromatics such as benzene, toluene, and xylene, esters such as butyl acetate, ketones such as acetone, 2-butanone, and cyclohexanone, nitrogen compounds such as N, N-dimethylformamide, and dichloromethane. , chlorobenzene, chloroform, and other halogenated hydrocarbons. Furthermore, the ink can be applied onto the base material by using a reverse roll coater, gravure coater, rod coater, air doctor coater, etc. (Yuji Harasaki, "Coating Method", published by Yoko Shoten, 1979). .

塗液の塗布方法としては、色素透過性低1度珊、滑剤層
の場合についても同様である。
The coating method for the coating liquid is the same for the dye permeability low 1 degree coral and lubricant layers.

色素高濃度層の厚みは、色素高濃度層中の色素濃度、目
標とする記録回数または相対速度比そして必要な最高記
録1度を得るために受像体上に必要な色素量に依存する
が、最低限下記の式で与えられる乾繰塗工重量は確保す
ることが好ましい。
The thickness of the dye-rich layer depends on the dye concentration in the dye-rich layer, the target number of recordings or relative speed ratio, and the amount of dye required on the image receptor to obtain the required maximum recording once. It is preferable to ensure at least the dry coating weight given by the following formula.

最低乾爆塗工重量(g/m2)= (目標記録回数)×
(必要色素量g/m2)/(色素重量濃度)色素透過性
低濃度層に用いる水、溶性樹脂及び水分散性樹脂として
は、ポリビニルアルコール、ポリ(メタ)アクリル酸(
金属塩も可)、ポリアクリルアミド、水性ウレタン樹脂
、水性アクリル樹脂、水性ポリエステル樹脂などを挙げ
ることができる(「水溶性亮分子 水分散性樹脂の最近
加工・改質技術と用途開発 総合技術資料集」 経営開
発センター出版 1981年 参照)。しかしながら、
例えば高鹸化度のポリビニルアルコールやアクリル酸の
ホモポリマなどは色素の拡散速度が小さく、層厚みが大
きくなると十分な記録感度を得ることができず、また厚
み変動の記録感度−多数回記録特性への影響が大きく実
用的ではない。
Minimum dry blast coating weight (g/m2) = (Target number of records) x
(Required amount of dye g/m2)/(Dye weight concentration) The water, soluble resin, and water-dispersible resin used for the dye permeability low concentration layer include polyvinyl alcohol, poly(meth)acrylic acid (
Metal salts are also allowed), polyacrylamide, water-based urethane resin, water-based acrylic resin, water-based polyester resin, etc. ” Management Development Center Publishing, 1981). however,
For example, with highly saponified polyvinyl alcohol or acrylic acid homopolymers, the dye diffusion rate is low, and if the layer thickness becomes large, sufficient recording sensitivity cannot be obtained. It has a large impact and is not practical.

適当な色素の拡散速度を宵する水溶性樹脂または水分散
性樹脂としては、鹸化度が30〜90%であるポリビニ
ルアルコール、水溶性(あるいは水分散性)ポリエステ
ル樹脂、水溶性(あるいは水分散性)ポリウレタン樹脂
、水溶性(あるいは水分散性)アクリル樹脂などを挙げ
ることができる。
Examples of water-soluble resins or water-dispersible resins that provide an appropriate dye diffusion rate include polyvinyl alcohol with a degree of saponification of 30 to 90%, water-soluble (or water-dispersible) polyester resins, and water-soluble (or water-dispersible) resins. ) polyurethane resin, water-soluble (or water-dispersible) acrylic resin, etc.

さらに、色素高濃度層と色素透過性低濃度層と滑剤層と
を順次積層する場合、滑剤層塗液によって色素透過性低
濃度層が侵されてしまうと色材層表面の色素濃度が適当
な濃度よりも高くなって、多数回記録特性が悪くなくな
ってしまう。このような場合には、色素透過性低濃度層
の樹脂が耐有機゛溶剤性を有しなければならない。この
ような水溶性または水分散性樹脂としては、鹸化度が7
0〜90%のポリビニルアルコール、水溶性(または水
分散性)ポリウレタン樹脂などを挙げることができる。
Furthermore, when a high dye concentration layer, a low dye permeability layer, and a lubricant layer are sequentially laminated, if the dye permeability low concentration layer is attacked by the lubricant layer coating liquid, the dye concentration on the surface of the coloring material layer cannot be adjusted to an appropriate level. The density becomes higher than the density, and the recording characteristics deteriorate many times. In such a case, the resin of the dye-permeable low concentration layer must have organic solvent resistance. Such water-soluble or water-dispersible resins have a saponification degree of 7.
Examples include 0 to 90% polyvinyl alcohol, water-soluble (or water-dispersible) polyurethane resin, and the like.

また、色素透過性低濃度層が滑剤を含む場合、使用でき
る滑剤は水系塗液に溶解または乳化できるものであれば
、特に限定されるものではなく、後記の滑剤層に使用さ
れる滑剤などが挙げられる。
In addition, when the dye-permeable low concentration layer contains a lubricant, the lubricant that can be used is not particularly limited as long as it can be dissolved or emulsified in the water-based coating solution, and the lubricant used in the lubricant layer described later can be used. Can be mentioned.

色素透過性低濃度層を形成するためのインク調製に使用
する溶剤としては、水辺外にアルコール類、ケトン類、
セロソルブ類などを添加しても良い。滑剤の乳化にあた
って、適当な乳化剤を添加することや、塗液の表面張力
を低下させるためにかくし界面活性剤を添加することは
差し支えないのはいうまでもない。
The solvents used for preparing the ink to form the dye-permeable low concentration layer include alcohols, ketones,
Cellosolves and the like may be added. It goes without saying that an appropriate emulsifier may be added to emulsify the lubricant, and a hidden surfactant may be added to reduce the surface tension of the coating liquid.

色素透過性低濃度層の厚みは、用いる水溶性樹脂または
水分散性樹脂の色素拡散速度や色素濃度あるいは目標と
する記録に必要なエネルギー 記録回数または相対速度
記録での相対速度比nなどに応じて調製することができ
るが、記録回数またはnが数10程度では厚みは0.1
〜1μm程度が適当である。
The thickness of the dye-permeable low-density layer depends on the dye diffusion rate and dye concentration of the water-soluble or water-dispersible resin used, the energy required for the target recording, the number of recordings, or the relative velocity ratio n in relative velocity recording. However, when the number of recordings or n is about several tens, the thickness is 0.1
Approximately 1 μm or so is appropriate.

滑剤層は少なくとも滑剤を含まなければならな滑剤層や
色素透過性低濃度層に含まれる滑剤としては、例えば流
動パラフィン等石油系潤滑油、シリコーン油、フッ素シ
リコーン油等合成潤滑油、各種変性シリコーン油(エポ
キシ変性1.アミン変性、アルキル変性、ポリエーテル
変性等)、ポリオキシアルキレングリコール等の宵機化
合物とシリコーンの共重合体等のシリコーン系潤滑性物
質、フルオロアルキル化合物等各種フッ素系界面活性剤
、三弗化塩化エチレン低重合物等のフッ素系潤滑性物質
、パラフィンワックス、ポリエチレンワックス等のワッ
クス類、高級脂肪族アルコール、高級アルコール、高級
脂肪酸アミド、高級脂肪酸エステル、高級脂肪酸塩等が
ある。このうち液状滑剤は、記録のための加熱が行われ
ない状態でも液状滑剤に色素が溶解した状態で受像体に
転移してしまうことがあるので好ましいとはいえない。
The lubricant layer must contain at least a lubricant. Examples of the lubricant contained in the lubricant layer and dye-permeable low concentration layer include petroleum-based lubricants such as liquid paraffin, synthetic lubricants such as silicone oil and fluorosilicone oil, and various modified silicones. Oils (epoxy-modified 1. Amine-modified, alkyl-modified, polyether-modified, etc.), silicone-based lubricating substances such as copolymers of silicone and Yoki compounds such as polyoxyalkylene glycol, various fluorine-based surfactants such as fluoroalkyl compounds, etc. agents, fluorine-based lubricating substances such as trifluorochloroethylene low polymers, waxes such as paraffin wax and polyethylene wax, higher aliphatic alcohols, higher alcohols, higher fatty acid amides, higher fatty acid esters, higher fatty acid salts, etc. . Among these, liquid lubricants are not preferred because the dye may be dissolved in the liquid lubricant and transferred to the image receptor even when heating for recording is not performed.

好ましくは、融点が60°C以上のワックス(更に各種
溶剤への溶解度の点において好ましくは、パラフィンワ
ックス、マイクロワックス)、脂肪酸アミド、脂肪酸、
反応性シリコーンオイルの反応物(無触媒で反応すると
いう点において好ましくは、エポキシ変性シリコーンオ
イルとアミノ変性シリコーンオイルの反応物)などがあ
る。これらは必要に応じて選択かつ組み合わせて使用す
ることが出来る。
Preferably, a wax with a melting point of 60°C or higher (more preferably paraffin wax or microwax in terms of solubility in various solvents), fatty acid amide, fatty acid,
Examples include a reaction product of reactive silicone oil (preferably a reaction product of epoxy-modified silicone oil and amino-modified silicone oil in terms of reacting without a catalyst). These can be selected and used in combination as necessary.

また、滑剤層は必要に応じて結着樹脂を含んでいても良
く、色素高濃度層に用いることができる各種結着樹脂の
他、水溶性樹脂、水分散性樹脂などを使用することがで
きる。しかしながら、染料転写体の記録特性を低下させ
ないように、色素の拡散速度が低くないものを用いるこ
とが好ましい。
Furthermore, the lubricant layer may contain a binder resin if necessary, and in addition to various binder resins that can be used in the dye-rich layer, water-soluble resins, water-dispersible resins, etc. can be used. . However, it is preferable to use a dye that does not have a low diffusion rate so as not to deteriorate the recording properties of the dye transfer member.

受像体は1通常受像基体と染着層から構成される。An image receptor usually consists of an image-receiving substrate and a dyeing layer.

受像基体としては、通常透明なものとしてはポリエステ
ル等の各種フィルム、白色のものとしてはポリエステル
、ポリプロピレン、等を主とした合成紙あるいはコート
紙、普通紙等が目的の応じて用いられる。
As image-receiving substrates, various transparent films such as polyester films are generally used, and white materials such as synthetic paper mainly made of polyester, polypropylene, etc., coated paper, plain paper, etc. are used depending on the purpose.

染着層に用いる染着性物質としてはポリエステル、ポリ
アミド、アクリル樹脂、アセテート樹脂、各種セルロー
ス誘導体、デンプン、ポリビニルアルコール等があり、
更に硬化樹脂としては、アクリル酸、アクリル酸エステ
ル、ポリエーテル、ポリウレタン、ポリアミド、アセテ
ート等の熱、光、電子線等による硬化物があり、必要に
応じて選択、組み合わせて用いられる。
The dyeable substances used in the dyeing layer include polyester, polyamide, acrylic resin, acetate resin, various cellulose derivatives, starch, polyvinyl alcohol, etc.
Further, as the cured resin, there are products cured by heat, light, electron beam, etc. such as acrylic acid, acrylic ester, polyether, polyurethane, polyamide, acetate, etc., and these may be selected and used in combination as necessary.

以下具体的実施例により本発明の詳細な説明する。The present invention will be explained in detail below using specific examples.

染料転写体の基体としては芳香族ポリアミドフィルム(
6μm厚)に耐熱滑性層を設けたものを共通に用いた。
Aromatic polyamide film (
6 μm thick) with a heat-resistant slipping layer provided thereon was commonly used.

受像体の基体としてはPET製白色白色合成紙用し、こ
の上に紫外線硬化樹脂(昭和高分子(株)SP5003
)Log、増感剤(日本チバガイギー(株)イルガキュ
ア184)0゜1 gs  アミド変性シリコーンオ、
イル(信越化学(株)KF3935)0.05gをトル
エン10gに溶解した塗液をワイヤーバーにて塗布した
後、熱風乾燥し、さらに1kW高圧水銀灯で1分間紫外
線を照射して硬化させ、染着層を形成して受像体とした
。使用した染料は下記の構造式のものである。
The base of the image receptor is PET white synthetic paper, and on top of this is an ultraviolet curing resin (Showa Kobunshi Co., Ltd. SP5003).
) Log, sensitizer (Nippon Ciba Geigy Co., Ltd. Irgacure 184) 0°1 gs amide-modified silicone,
After applying a coating solution of 0.05 g of Illu (Shin-Etsu Chemical Co., Ltd. KF3935) dissolved in 10 g of toluene using a wire bar, it was dried with hot air, and then cured by irradiating ultraviolet rays for 1 minute with a 1 kW high-pressure mercury lamp to dye it. A layer was formed to form an image receptor. The dye used has the following structural formula.

記録手段としてはサーマルヘッドを使用し、記録茶件と
しては 記録周期     16. 7−  ms/1記録パル
ス幅  MAX 4. 0  ms解像度      
 6   1 /mm記録エネルギー   6    
J/cm2(可変)転写体走行速度   1. 0  
mm/s  ※受像体走行速度  10. 0  mm
/sを基本とした(※ 相対速度記録の場合のみ、単純
繰り返し記録では10. 0  mm/sである)。
A thermal head is used as the recording means, and the recording period is the recording period.16. 7-ms/1 recording pulse width MAX 4. 0 ms resolution
6 1 /mm recording energy 6
J/cm2 (variable) Transfer body running speed 1. 0
mm/s *Image receptor traveling speed 10. 0mm
/s (*Only in the case of relative velocity recording, simple repeat recording is 10.0 mm/s).

〈実施例1〉 基体上に上記の構造式の染料2gと結着樹脂としてブチ
ラール樹脂(漬水化学(株)エスレックBX−1)2g
をトルエン21g1 MEK9gの混合溶媒に溶かした
インクをワイヤーバーで乾燥塗工重量が3 g/Iにな
るように塗布し乾燥し、色素高濃度層を設けた。そして
水溶性飽和ポリエステル樹脂(日本合成化学(株)ポリ
エスタ−WR901)1g、  ポリビニルアルコール
(日本合成化学(株)ゴーセノールKH−17)0.1
gを水20gに溶解した塗液をワイヤーバーで乾燥塗工
重量が0.2g/m2になるように塗布し乾燥して色素
透過性低濃度層を設けた。さらにブチラール樹脂(漬水
化学(株)エスレックBMS)1g1  融°点69°
Cのパラフィンワックス(日本精蝋(株)品番155)
0.05g1 オレイン酸アミド0.05gをトルエン
15gに溶解した塗液をワイヤーバーで乾燥塗工重量が
0.2g/m2になるように塗布し乾燥して滑剤層を設
け、色材層とし、染料転写体を得た。
<Example 1> 2 g of the dye having the above structural formula and 2 g of butyral resin (S-LEC BX-1 manufactured by Tsukisui Kagaku Co., Ltd.) as a binder resin were placed on the substrate.
An ink prepared by dissolving this in a mixed solvent of 21 g of toluene and 9 g of MEK was coated with a wire bar so that the dry coating weight was 3 g/I and dried to form a high dye concentration layer. and 1 g of water-soluble saturated polyester resin (Nippon Gosei Kagaku Co., Ltd. Polyester-WR901), 0.1 g of polyvinyl alcohol (Nippon Gosei Kagaku Co., Ltd. Gohsenol KH-17).
A coating solution prepared by dissolving 1.0 g in 20 g of water was applied using a wire bar to a dry coating weight of 0.2 g/m2, and dried to form a dye-permeable low concentration layer. In addition, 1g1 of butyral resin (S-LEC BMS, Tsukusui Kagaku Co., Ltd.) melting point 69°
C paraffin wax (Nippon Seiro Co., Ltd. product number 155)
0.05g1 A coating solution prepared by dissolving 0.05g of oleic acid amide in 15g of toluene was applied using a wire bar so that the dry coating weight was 0.2g/m2, and dried to form a lubricant layer, which was then used as a coloring material layer. A dye transfer body was obtained.

〈実施例2〉 実施例1と同様にして色素高濃度層を設けた後、45%
鹸化ポリビニルアルコール1gを水7.5g1  エタ
ノール7.5gの混合溶媒に溶解した塗液を乾燥塗工重
量が0.2g/m2になるようにして塗布し乾燥して染
料転写体とした。
<Example 2> After providing a high dye concentration layer in the same manner as in Example 1, 45%
A coating solution prepared by dissolving 1 g of saponified polyvinyl alcohol in a mixed solvent of 7.5 g of water and 7.5 g of ethanol was applied to give a dry coating weight of 0.2 g/m 2 and dried to obtain a dye transfer material.

〈実施例3〉 実施例1と同様にして色素高濃度層と設けた後、水分散
ウレタンアイオノマー樹脂溶液(大日本インキ(株)ハ
イトランAP40  固形分22重重篤)5g1 ポリ
ビニルアルコール(日本合成化学(株)ゴーセノールK
H−17)0.02gを水12.5gに希釈・溶解した
塗液を乾燥塗工重量が0.2gになるように塗布し乾燥
して色素透過性低濃度層とした。さらにブチラール樹脂
(同BMS)1g1 アミノ変性シリコーンオイル(信
越化学(株) KF 393) O−05gz  xホ
4シ変性シリコーンオイル(信越化学(株)X−22−
393)0.05gをトルエン15gに溶解した塗液を
同様にして塗布し乾燥して染料転写体とした。
<Example 3> After forming a high dye concentration layer in the same manner as in Example 1, a water-dispersed urethane ionomer resin solution (Dainippon Ink Co., Ltd. Hytran AP40, solid content 22%), 5 g 1 polyvinyl alcohol (Nippon Gosei Chemical Co., Ltd.) GOHSENOL K Co., Ltd.
A coating solution prepared by diluting and dissolving 0.02 g of H-17) in 12.5 g of water was applied to a dry coating weight of 0.2 g and dried to form a dye-permeable low concentration layer. In addition, butyral resin (BMS) 1g1 Amino-modified silicone oil (Shin-Etsu Chemical Co., Ltd. KF 393) O-05gz
A coating solution in which 0.05 g of 393) was dissolved in 15 g of toluene was applied in the same manner and dried to obtain a dye transfer material.

〈実施例4〉 実施例1と同様にして色素高1度層を設けた後、45%
鹸化ポリビニルアルコール1g1 融点69°Cのパラ
フィンワックス(同)0.05g、  オレイン酸アミ
ド0.05g、  界面活性剤(花王(株)レオドール
430)0.002gを水7.5g1エタノール7.5
gの混合溶媒に溶解・乳化した塗液を乾燥塗工重量が0
.2g/m2になるようにして塗布し乾燥して染料転写
体とした。
<Example 4> After providing a dye high 1 degree layer in the same manner as in Example 1, 45%
1g of saponified polyvinyl alcohol, 0.05g of paraffin wax with a melting point of 69°C, 0.05g of oleic acid amide, 0.002g of surfactant (Rheodol 430, Kao Corporation), 7.5g of water, 7.5g of ethanol.
The dry coating weight of the coating liquid dissolved and emulsified in g of mixed solvent is 0.
.. It was coated at a concentration of 2 g/m 2 and dried to obtain a dye transfer material.

く比較例1〉 実施例1と同様にして色素高濃9度層を設けて染料転写
体とした。
Comparative Example 1> In the same manner as in Example 1, a high dye concentration 9 degree layer was provided to prepare a dye transfer body.

く比較例2〉 実施例1と同様にして色素高濃度層を設けた後、ブチラ
ール樹脂(同 BX−1)Igl 融点69℃のパラフ
ィンワックス(同)0.05g1 オレイン酸アミド0
.05gをトルエン21g1 MEK9gに溶解した塗
液を乾燥塗工重量が0.8gになるように塗布し乾燥し
て色素透過性低濃度層を設けて染料転写体とした。但し
この場合、色素透過性低濃度層を塗布した後のワイヤー
バーには大量の染料が溶解した塗液が付着していた。
Comparative Example 2> After providing a high dye concentration layer in the same manner as in Example 1, butyral resin (BX-1) Igl, paraffin wax (same) with a melting point of 69°C 0.05 g 1 oleic acid amide 0
.. A coating solution prepared by dissolving 0.5 g of toluene in 21 g of toluene and 9 g of MEK was coated so that the dry coating weight was 0.8 g, and dried to form a dye-permeable low-density layer to prepare a dye transfer body. However, in this case, a large amount of coating liquid containing dissolved dye was attached to the wire bar after the dye-permeable low concentration layer was applied.

く比較例3〉 実施例1と同様にして色素高濃度層を設けた後、ポリビ
ニルアルコール((株)タラレ ポバールt17)Ig
を20gの水に溶解した塗液を乾燥塗工重量が0.1g
/m2になるように塗布し乾燥して色素透過性低濃度層
とした。さらにブチラール樹脂(同 BMS)Ig、 
 アミノ変性シリコーンオイル(信越化学(株)KF3
93)0.05g1  エポキシ変性シリコーンオイル
(信越化学(株)X−22−393)0.05gをトル
エン15gに・溶解した塗液を同様にして塗布し乾燥し
て染料転写体とした 以上のような染料転写体を前記条件で記録に供し、相対
速度記録の可否を調べた。結果は第1表及び第4図のよ
うになった。
Comparative Example 3 After providing a high dye concentration layer in the same manner as in Example 1, polyvinyl alcohol (Tarare Poval T17) Ig
The dry coating weight is 0.1g by dissolving the coating liquid in 20g of water.
/m2 and dried to form a dye-permeable low concentration layer. In addition, butyral resin (BMS) Ig,
Amino-modified silicone oil (Shin-Etsu Chemical Co., Ltd. KF3)
93) 0.05g1 0.05g of epoxy-modified silicone oil (Shin-Etsu Chemical Co., Ltd. X-22-393) was dissolved in 15g of toluene, and a coating liquid was applied in the same manner and dried to make a dye transfer material. The dye transfer material was subjected to recording under the above conditions to examine whether relative speed recording was possible. The results were as shown in Table 1 and Figure 4.

第4図においては、単純繰り返し方式多数回記録におけ
る同一記録エネルギーでの記録濃度変化=N回目の記録
濃度/1回目の記録1度(%)を測定した。
In FIG. 4, the recording density change at the same recording energy in multiple recordings using the simple repetition method=Nth recording density/first recording degree (%) was measured.

く第1表〉 ※記録エネルギーは、記録濃度が約1.8になるエネル
ギーを示す。単位はJ/crn2発明の効果 本発明によれば、多数回記録における、繰り返し回数の
増加に伴う色材層表面の色素濃度の急激な低下が抑えら
れ、記録濃度の低下が大きく改善される。また、滑剤を
含むことによって滑性を付与した染料転写体は、相対速
度記録も可能になる。
Table 1 *Recording energy indicates the energy at which the recording density becomes approximately 1.8. The unit is J/crn2 Effects of the Invention According to the present invention, the rapid decrease in dye density on the surface of the coloring material layer due to the increase in the number of repetitions in multiple recordings is suppressed, and the decrease in recording density is greatly improved. Furthermore, a dye transfer material imparted with lubricity by containing a lubricant can also perform relative velocity recording.

その結果、実用性の高い高耐侯性低昇華性の色素が使用
可能で、同一記録エネルギーに対する記録回数増に伴う
記録濃度低下が小さく、より多数回まで高い飽和記録濃
度を保持することができ、より低いランニングコストで
通常の1回記録と同等のフルカラー記録を可能とする多
数回記録用染料転写体を得ることができる。
As a result, it is possible to use highly practical dyes with high weather resistance and low sublimation, and the decrease in recording density due to the increase in the number of recordings for the same recording energy is small, making it possible to maintain high saturated recording density for many more recordings. It is possible to obtain a dye transfer material for multi-time recording that enables full-color recording equivalent to normal one-time recording at lower running costs.

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

第1図、および第3図は本発明の実施例における染料転
写体の断面図、第2図は相対速度記録方式多数回記録の
原理図、第4図は本発明の具体的実施例における多数回
記録濃度特性を示す図である。 1・・・・転写体、3・・・・色材層、4・・・・受像
体、6・・・・染着層、9・・・・色素高濃度層、10
・・・・色素透過性低濃度層、11・・・・滑剤層。 代理人の氏名 弁理士 中尾敏男 はか1名第1図 第3図 第4図 1転写体 第2図 記録回数N
1 and 3 are cross-sectional views of a dye transfer body in an embodiment of the present invention, FIG. 2 is a principle diagram of multiple recording using the relative speed recording method, and FIG. FIG. 3 is a diagram showing the recording density characteristics. DESCRIPTION OF SYMBOLS 1...Transfer body, 3...Color material layer, 4...Image receptor, 6...Dyeing layer, 9...Dye high concentration layer, 10
...Dye-permeable low concentration layer, 11...Lubricant layer. Name of agent Patent attorney Toshio Nakao (1 person) Figure 1 Figure 3 Figure 4 Figure 1 Transcript Figure 2 Number of recordings N

Claims (5)

【特許請求の範囲】[Claims] (1)少なくとも色素を含む色素高濃度層と、層中の色
素濃度が前記高濃度層より低く、少なくとも水溶性樹脂
または水分散性樹脂を含む色素透過性低濃度層とを、基
体上に順次積層して色材層とした染料転写体。
(1) A dye high concentration layer containing at least a dye and a dye permeable low concentration layer having a dye concentration lower than that of the high concentration layer and containing at least a water-soluble resin or a water-dispersible resin are sequentially formed on a substrate. A dye transfer material that is laminated to form a color material layer.
(2)色素透過性低濃度層が更に滑剤を含む特許請求の
範囲第1項記載の染料転写体。
(2) The dye transfer member according to claim 1, wherein the dye-permeable low-density layer further contains a lubricant.
(3)色素透過性低濃度層上に更に、少なくとも滑剤を
含む滑剤層を積層して色材層とした特許請求の範囲第1
項記載の染料転写体。
(3) A lubricant layer containing at least a lubricant is further laminated on the dye permeable low concentration layer to form a coloring material layer.
Dye transfer material described in Section 1.
(4)色素低濃度層の水溶性樹脂または水分散性樹脂が
、部分鹸化ポリビニルアルコール、水溶性飽和ポリエス
テル樹脂、または水分散性ポリウレタン樹脂である特許
請求の範囲第1項記載の染料転写体。
(4) The dye transfer member according to claim 1, wherein the water-soluble resin or water-dispersible resin of the low dye concentration layer is partially saponified polyvinyl alcohol, water-soluble saturated polyester resin, or water-dispersible polyurethane resin.
(5)少なくとも色素を含む有機溶剤系塗液と、固形分
中の色素濃度が前記有機溶剤系塗液の固形分中の色素濃
度よりも低く少なくとも水溶性樹脂または水分散性樹脂
を含む水系塗液とを、基体上に順次積層して少なくとも
色素高濃度層と色素透過性低濃度層からなる色材層を構
成することを特徴とする染料転写体の製造方法。
(5) an organic solvent-based coating liquid containing at least a pigment, and a water-based coating containing at least a water-soluble resin or a water-dispersible resin, the dye concentration of which is lower in the solid content than the pigment concentration in the solid content of the organic solvent-based coating liquid; 1. A method for producing a dye transfer material, which comprises sequentially layering a dye transfer material on a substrate to form a color material layer consisting of at least a high dye concentration layer and a low dye permeability layer.
JP63144242A 1988-03-04 1988-06-10 Dye transfer body and manufacturing method thereof Expired - Fee Related JP2502683B2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP63144242A JP2502683B2 (en) 1988-06-10 1988-06-10 Dye transfer body and manufacturing method thereof
EP89302175A EP0331525B1 (en) 1988-03-04 1989-03-03 Method for thermal dye transfer printing, dye transfer sheets and method for making same, dye receiving sheets and a thermal printing system
US07/318,588 US5137865A (en) 1988-03-04 1989-03-03 Method for thermal dye transfer printing, dye transfer sheets and method for making same, dye receiving sheets and a thermal printing system
CA000592655A CA1327123C (en) 1988-03-04 1989-03-03 Method for thermal dye transfer printing, dye transfer sheets and method for making same, dye receiving sheets and a thermal printing system
DE68918883T DE68918883T2 (en) 1988-03-04 1989-03-03 Thermal transfer printing process, dye transfer layers and process for their production, dye receiving layers and a thermal printing system.
US07/905,990 US5334574A (en) 1988-03-04 1992-06-29 Method for thermal dye transfer printing, dye transfer sheets and method for making same, dye receiving sheets and a thermal printing system

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63144242A JP2502683B2 (en) 1988-06-10 1988-06-10 Dye transfer body and manufacturing method thereof

Publications (2)

Publication Number Publication Date
JPH022077A true JPH022077A (en) 1990-01-08
JP2502683B2 JP2502683B2 (en) 1996-05-29

Family

ID=15357549

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63144242A Expired - Fee Related JP2502683B2 (en) 1988-03-04 1988-06-10 Dye transfer body and manufacturing method thereof

Country Status (1)

Country Link
JP (1) JP2502683B2 (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0211388A (en) * 1988-06-30 1990-01-16 Ricoh Co Ltd Sublimation-type thermal transfer recording method
JPH0225389A (en) * 1988-07-15 1990-01-26 Ricoh Co Ltd Sublimation-type thermal transfer recording medium
JPH0226790A (en) * 1988-07-18 1990-01-29 Ricoh Co Ltd Sublimable type thermal transfer medium
JPH0239994A (en) * 1988-07-29 1990-02-08 Ricoh Co Ltd Sublimation-type thermal transfer medium
JPH0250888A (en) * 1988-08-11 1990-02-20 Ricoh Co Ltd Sublimating type thermal transfer recording medium
JPH0269293A (en) * 1988-09-05 1990-03-08 Ricoh Co Ltd Sublimating thermal transfer medium
JPH02227292A (en) * 1989-02-28 1990-09-10 Ricoh Co Ltd Sublimable thermal transfer recording medium
JPH02227291A (en) * 1989-02-28 1990-09-10 Ricoh Co Ltd Sublimable thermally transferrable recording medium
JPH02229077A (en) * 1989-03-01 1990-09-11 Ricoh Co Ltd Sublimable thermal transfer recording method
JPH02231191A (en) * 1989-03-03 1990-09-13 Ricoh Co Ltd Sublimable thermal transfer recording method
JPH0592673A (en) * 1991-09-30 1993-04-16 Toppan Printing Co Ltd Thermal transfer recording medium

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0211388A (en) * 1988-06-30 1990-01-16 Ricoh Co Ltd Sublimation-type thermal transfer recording method
JPH0225389A (en) * 1988-07-15 1990-01-26 Ricoh Co Ltd Sublimation-type thermal transfer recording medium
JPH0226790A (en) * 1988-07-18 1990-01-29 Ricoh Co Ltd Sublimable type thermal transfer medium
JPH0239994A (en) * 1988-07-29 1990-02-08 Ricoh Co Ltd Sublimation-type thermal transfer medium
JPH0250888A (en) * 1988-08-11 1990-02-20 Ricoh Co Ltd Sublimating type thermal transfer recording medium
JPH0269293A (en) * 1988-09-05 1990-03-08 Ricoh Co Ltd Sublimating thermal transfer medium
JPH02227292A (en) * 1989-02-28 1990-09-10 Ricoh Co Ltd Sublimable thermal transfer recording medium
JPH02227291A (en) * 1989-02-28 1990-09-10 Ricoh Co Ltd Sublimable thermally transferrable recording medium
JPH02229077A (en) * 1989-03-01 1990-09-11 Ricoh Co Ltd Sublimable thermal transfer recording method
JPH02231191A (en) * 1989-03-03 1990-09-13 Ricoh Co Ltd Sublimable thermal transfer recording method
JPH0592673A (en) * 1991-09-30 1993-04-16 Toppan Printing Co Ltd Thermal transfer recording medium

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