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JPH0333118B2 - - Google Patents

Info

Publication number
JPH0333118B2
JPH0333118B2 JP59032201A JP3220184A JPH0333118B2 JP H0333118 B2 JPH0333118 B2 JP H0333118B2 JP 59032201 A JP59032201 A JP 59032201A JP 3220184 A JP3220184 A JP 3220184A JP H0333118 B2 JPH0333118 B2 JP H0333118B2
Authority
JP
Japan
Prior art keywords
resin composition
transfer
solvent
transfer layer
colorant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP59032201A
Other languages
Japanese (ja)
Other versions
JPS60176798A (en
Inventor
Kazuo Matsunaga
Takashi Kagami
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.)
Toppan Inc
Original Assignee
Toppan Printing 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 Toppan Printing Co Ltd filed Critical Toppan Printing Co Ltd
Priority to JP59032201A priority Critical patent/JPS60176798A/en
Publication of JPS60176798A publication Critical patent/JPS60176798A/en
Publication of JPH0333118B2 publication Critical patent/JPH0333118B2/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
    • B41M5/38207Contact thermal transfer or sublimation processes characterised by aspects not provided for in groups B41M5/385 - B41M5/395

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]

(産業上の利用分野) 本発明は、熱転写性がすぐれ、かつ転写後の被
転写物の表面性能のすぐれた取扱い容易な感熱転
写フイルムの製造方法に関する。 (従来技術) 従来よりサーマルヘツドを用いる感熱転写記録
法に適する感熱転写フイルムとして、例えばポリ
エステルフイルムやコンデンサー紙の如き薄手の
基材上に着色剤を含むワツクスを主成分とする転
写層を形成したものが知られている。しかしなが
ら、従来から使用されている感熱転写フイルムは
単一の転写層で構成されている為に、感熱転写フ
イルムに要求される主要な性質、すなわち、熱転
写性、転写後の被転写物の表面性能、転写フイル
ムの操作性等をすべて満足することは困難であ
り、これらを解決した転写フイルムの出現が要望
されていた。 従来このために為された主な努力は、転写層の
組成面から見ると、熱転写性向上のための低融
点、低溶融粘度化と、転写フイルムの操作性、保
存性および被転写物の表面性能、印字品位向上の
ための高融点、高溶融粘度化の2つの方向のバラ
ンスをとり、これらを両立させるために転写時の
加熱に対する敏感性、即ち溶融粘度の極めて狭い
温度領域内における急激な変化を追求することで
あつた。このような努力は感熱転写層の組成の基
本的な検討として多くの成果を上げたものの結果
として完全に満足を与えるところまで到達してい
ない。 (目的) 本発明者等は、種々検討の結果、先に挙げた3
点を満たすためには単一の転写層ではなく、複合
された転写層が望ましいとの結論に達し、本発明
を完成するに至つた。以下、本発明に至る経過を
詳細に説明する。 (構成〕 本発明において、基材としては、熱伝導率が良
く、耐熱性、強度のある薄いフイルム、紙等が、
代表的にはコンデンサー紙やポリエステルフイル
ムが使用される。 また、バインダーとしては、天然ワツクス、合
成ワツクス等のワツクス類、及び要すればその他
の熱可塑性樹脂類が、着色剤としては、一般に公
知である有機顔料、無機顔料、染料が使用され
る。溶剤分散型樹脂組成物は、転写フイルムの製
造工程中に揮散ないし蒸発するような液状分散媒
に上記バインダー、着色剤が分散された組成物で
あり、熱溶融型樹脂組成物は、本質的にはそのま
ま転写層の一部となるような上記バインダーと着
色剤の混合物であり、従つて、常温で固型、かつ
塗工時に熱により溶融して液状となるものを指
す。 当初、本発明者等は複合された転写層の形成に
あたつて、熱溶融型樹脂組成物を重ねて塗工する
方法、及び溶剤分散型樹脂組成物を重ねて塗工す
する方法の両者を検討したが、第1の方法におい
ては、はじめに塗工する樹脂組成物と次に塗工す
る樹脂組成物との融点が接近すると塗工時に両者
が混合してしまい、均一な塗膜層を形成できなか
つた。第2の方法においては、転写エネルギーが
高くなり、転写性の面で満足のいく結果が得られ
なかつた。両者に共通する問題点は、彦転写物の
表面性能を高めるためのはじめの塗工層に対し
て、転写性を高めるための次の塗工層は融点と溶
融粘度を大幅に下げなければならず、そのために
転写フイルムのブロツキングや裏移りが生じるこ
とであつた。この過程を詳細に検討した結果、本
発明者等は次の注目すべき結果に着目した。即
ち、転写層としては本質的に同一の組成である溶
剤分散型樹脂組成物で形成した転写層と、熱溶融
型樹脂組成物で形成した転写層とでは、明らかに
前者の方が必要とする転写エネルギーが高く、基
材への密着が良いという結果である。この理由に
ついては、工程中の熱履歴、基材のテンシヨン、
基材への組成物のぬれ等、様々な要因が考えられ
るが、推測の域を出ていない。 以上の結果より本発明者等は、基材に接する転
写層として溶剤分散型樹脂組成物で形成した層
を、さらに被転写物に接する転写層として熱溶融
型樹脂組成物で形成した層を有する転写フイルム
により、先に述べた転写性、転写後の被転写物の
表面性能、転写フイルムの取扱いの容易さの3点
をともに満足する転写フイルムを得ることができ
ると確信するに至り、更に検討の結果、本発明の
完成に至つた。 即ち、本発明の要旨とするところは、基材の一
方の面に、加熱により溶融する樹脂組成物と着色
剤を溶剤中に分散した溶剤分散型樹脂組成物を塗
布し、乾燥して溶剤を揮散させて第1の転写層を
形成し、次いでその上に、加熱により溶融する樹
脂組成物中に着色剤を配合した熱溶融型樹脂組成
物を加熱溶融状態で塗工し、冷却して第2の転写
層を形成することを特徴とする感熱転写フイルム
の製造方法である。 (効果) 本発明は以上の如く、ほぼ同一の組成でありな
がら塗工時の状態が異なる2種類の組成物を塗布
して転写層を形成することにより、 (1) 基材への密着性の向上、従つてもみ落ち、基
材からの剥がれの防止。 (2) 被転写物に接する層のブロツキングの起らな
い範囲での低融点、低溶融粘度化、従つて同じ
印加エネルギーに対する転写性の向上。 を実現したことになるが、さらに、基材への密着
性が向上した樹脂層の上から熱溶融型樹脂組成物
を塗工する場合の方が、熱溶融型樹脂組成物で形
成された転写層の上から塗工する場合に比べて、
必要とする塗工温度の低下がより少ないという利
点があげられる。これらは各樹脂組成物の選択の
巾をより広げるものであり、従つて、溶剤分散型
樹脂組成物で形成した転写層と、熱溶融型樹脂組
成物で形成した転写層とが組成上同一である必要
もないのであつて、各転写層を目的に合わせて組
成を変えることを排除するのではないことは当然
である。 実施例 1 厚さ6μのポリエステルフイルム上にグラビア
コーターを用いて下記樹脂組成物を1.5g/m2
dryを塗工し、乾燥を60℃30秒行なつた後、更に
下記樹脂組成物を85℃の条件でグラビアコータ
ーを用いて2.0g/m2dryコーテイング後冷却し、
転写フイルムを作製した。 〔樹脂組成物〕 合成ワツクス(融点71℃) 22重量部 カーボンブラツク(着色剤) 25 〃 トルエン(溶剤) 75 〃 分散剤 0.2 〃 〔樹脂組成物〕 合成ワツクス(融点71℃) 110重量部 カーボンブラツク(着色剤) 12.5 〃 分散剤 1重量部 比較例として、樹脂組成物のみを同じポリエ
ステルフイルムに85℃の条件で3.5g/m2dry塗工
し、転写フイルムを作製した。これをベツク平滑
度計による測定値が200秒の紙に8dot/mmのサー
マルヘツドで、パルス幅1ms、印加エネルギー
0.2W/dotで転写したところ、以下の結果を得
た。
(Industrial Application Field) The present invention relates to a method for producing a heat-sensitive transfer film that has excellent heat transferability, excellent surface properties of the transferred object after transfer, and is easy to handle. (Prior art) Conventionally, as a thermal transfer film suitable for a thermal transfer recording method using a thermal head, a transfer layer mainly composed of wax containing a colorant is formed on a thin base material such as a polyester film or condenser paper. something is known. However, since conventionally used thermal transfer films are composed of a single transfer layer, the main properties required for thermal transfer films are thermal transferability and surface performance of the transferred object after transfer. It is difficult to satisfy all of the requirements such as easiness of use and operability of a transfer film, and there has been a demand for a transfer film that solves these problems. From the viewpoint of the composition of the transfer layer, the main efforts that have been made in the past have been to lower the melting point and melt viscosity to improve thermal transferability, improve the operability and storage stability of the transfer film, and improve the surface of the transferred material. In order to balance the two directions of high melting point and high melt viscosity to improve performance and printing quality, and to achieve both, it is important to reduce the sensitivity to heating during transfer, that is, the sudden change in melt viscosity within an extremely narrow temperature range. It was about pursuing change. Although these efforts have yielded many results in the basic study of the composition of thermal transfer layers, the results have not yet reached a point of complete satisfaction. (Purpose) As a result of various studies, the present inventors have
In order to satisfy the above requirements, the inventors came to the conclusion that a composite transfer layer rather than a single transfer layer is preferable, leading to the completion of the present invention. Hereinafter, the progress leading to the present invention will be explained in detail. (Structure) In the present invention, the base material is a thin film, paper, etc. that has good thermal conductivity, heat resistance, and strength.
Typically, condenser paper or polyester film is used. Further, as the binder, waxes such as natural waxes and synthetic waxes, and if necessary, other thermoplastic resins are used, and as the colorant, generally known organic pigments, inorganic pigments, and dyes are used. A solvent-dispersed resin composition is a composition in which the binder and colorant are dispersed in a liquid dispersion medium that volatilizes or evaporates during the transfer film manufacturing process. is a mixture of the above-mentioned binder and colorant that becomes part of the transfer layer as it is, and therefore refers to a mixture that is solid at room temperature and becomes liquid when it is melted by heat during coating. Initially, the present inventors used two methods to form a composite transfer layer: a method in which hot-melt resin compositions were applied in layers, and a method in which solvent-dispersed resin compositions were applied in layers. However, in the first method, if the melting points of the resin composition to be applied first and the resin composition to be applied next are close to each other, the two will mix during coating, making it difficult to form a uniform coating layer. could not be formed. In the second method, the transfer energy was high and satisfactory results could not be obtained in terms of transferability. The problem common to both is that the melting point and melt viscosity of the first coating layer to improve transferability must be significantly lowered compared to the first coating layer to improve the surface performance of Hiko transfers. First, this caused blocking and set-off of the transfer film. As a result of examining this process in detail, the present inventors noticed the following remarkable results. That is, between a transfer layer formed of a solvent-dispersed resin composition and a transfer layer formed of a hot-melt resin composition, which have essentially the same composition, the former is clearly more necessary. The results show that the transfer energy is high and the adhesion to the base material is good. The reasons for this include the thermal history during the process, the tension of the base material,
Various factors can be considered, such as wetting of the composition onto the base material, but this is still within the realm of speculation. Based on the above results, the present inventors have provided a layer formed of a solvent-dispersed resin composition as a transfer layer in contact with a substrate, and a layer formed of a hot-melt resin composition as a transfer layer in contact with an object to be transferred. We became convinced that we could obtain a transfer film that satisfies the three points mentioned above: transferability, surface performance of the transferred object after transfer, and ease of handling of the transfer film, so we conducted further research. As a result, the present invention was completed. That is, the gist of the present invention is to coat one side of a base material with a solvent-dispersed resin composition in which a resin composition that melts when heated and a colorant are dispersed in a solvent, and then dry to remove the solvent. The first transfer layer is formed by volatilization, and then a hot-melt resin composition containing a colorant in a resin composition that melts when heated is applied in a heated molten state, and then cooled to form a first transfer layer. This is a method for producing a heat-sensitive transfer film, which is characterized by forming a second transfer layer. (Effects) As described above, the present invention achieves (1) adhesion to the substrate by forming a transfer layer by applying two types of compositions that have almost the same composition but different states at the time of coating. Improves the quality of the product and prevents it from rubbing off and peeling off from the base material. (2) Lower melting point and lower melt viscosity without causing blocking of the layer in contact with the transferred material, thus improving transferability for the same applied energy. However, in addition, when applying a hot-melt resin composition over a resin layer with improved adhesion to the base material, it is better to apply a transfer formed with a hot-melt resin composition. Compared to coating from the top of the layer,
An advantage is that less reduction in coating temperature is required. These are intended to further expand the range of selection of each resin composition, and therefore, a transfer layer formed with a solvent-dispersed resin composition and a transfer layer formed with a hot-melt resin composition are compositionally the same. There is no need for it to exist, and it goes without saying that changing the composition of each transfer layer depending on the purpose is not excluded. Example 1 1.5 g/m 2 of the following resin composition was applied onto a 6μ thick polyester film using a gravure coater.
After applying dry and drying for 30 seconds at 60°C, further coat the following resin composition at 2.0g/m 2 dry using a gravure coater at 85°C, and then cool it.
A transfer film was produced. [Resin composition] Synthetic wax (melting point 71°C) 22 parts by weight Carbon black (colorant) 25 Toluene (solvent) 75 Dispersant 0.2 [Resin composition] Synthetic wax (melting point 71°C) 110 parts by weight Carbon black (Colorant) 12.5 Dispersant 1 part by weight As a comparative example, a transfer film was prepared by applying only the resin composition to the same polyester film at a rate of 3.5 g/m 2 dry at 85°C. This was measured using a Beck smoothness meter for 200 seconds using a thermal head of 8 dots/mm, a pulse width of 1 ms, and an applied energy.
When transferring at 0.2W/dot, the following results were obtained.

〔樹脂組成物〕[Resin composition]

合成ワツクス(融点73℃) 22重量部 カーボンブラツク(着色剤) 2.5 〃 トルエン(溶剤) 75 〃 分散剤 0.2 〃 〔樹脂組成物〕 合成ワツクス(融点64℃) 106重量部 カーボンブラツク(着色剤) 12.5 〃 分散剤 1 〃 オイル 4 〃 Synthetic wax (melting point 73℃) 22 parts by weight Carbon black (coloring agent) 2.5 〃 Toluene (solvent) 75 〃 Dispersant 0.2 〃 [Resin composition] Synthetic wax (melting point 64℃) 106 parts by weight Carbon black (colorant) 12.5 〃 Dispersant 1 Oil 4 〃

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 基材の一方の面に、加熱により溶融する樹脂
組成物と着色剤を溶剤中に分散した溶剤分散型樹
脂組成物を塗布し、乾燥して溶剤を揮散させて第
1の転写層を形成し、次いでその上に、加熱によ
り溶融する樹脂組成物中に着色剤を配合した熱溶
融型樹脂組成物を加熱溶融状態で塗工し、冷却し
て第2の転写層を形成することを特徴とする感熱
転写フイルムの製造方法。
1. A solvent-dispersed resin composition in which a resin composition that melts when heated and a colorant are dispersed in a solvent is applied to one side of the base material, and dried to volatilize the solvent to form a first transfer layer. Then, a hot-melt type resin composition in which a coloring agent is blended into a resin composition that melts when heated is applied thereon in a heated molten state, and then cooled to form a second transfer layer. A method for producing a thermal transfer film.
JP59032201A 1984-02-22 1984-02-22 Thermal transfer film Granted JPS60176798A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59032201A JPS60176798A (en) 1984-02-22 1984-02-22 Thermal transfer film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59032201A JPS60176798A (en) 1984-02-22 1984-02-22 Thermal transfer film

Publications (2)

Publication Number Publication Date
JPS60176798A JPS60176798A (en) 1985-09-10
JPH0333118B2 true JPH0333118B2 (en) 1991-05-15

Family

ID=12352291

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59032201A Granted JPS60176798A (en) 1984-02-22 1984-02-22 Thermal transfer film

Country Status (1)

Country Link
JP (1) JPS60176798A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58185294A (en) * 1982-04-24 1983-10-28 Canon Inc Transfer film capable of representing half tone
JPS58217392A (en) * 1982-06-14 1983-12-17 Konishiroku Photo Ind Co Ltd Heat-sensitive transfer recording medium
JPS59194894A (en) * 1983-04-20 1984-11-05 Fujitsu Ltd Multilayer ink sheet for thermal transfer recording
JPS59224392A (en) * 1983-06-04 1984-12-17 Canon Inc Thermal transfer material

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58185294A (en) * 1982-04-24 1983-10-28 Canon Inc Transfer film capable of representing half tone
JPS58217392A (en) * 1982-06-14 1983-12-17 Konishiroku Photo Ind Co Ltd Heat-sensitive transfer recording medium
JPS59194894A (en) * 1983-04-20 1984-11-05 Fujitsu Ltd Multilayer ink sheet for thermal transfer recording
JPS59224392A (en) * 1983-06-04 1984-12-17 Canon Inc Thermal transfer material

Also Published As

Publication number Publication date
JPS60176798A (en) 1985-09-10

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