JPS60219094A - Transfer material for thermal recording - Google Patents

Transfer material for thermal recording

Info

Publication number
JPS60219094A
JPS60219094A JP59076038A JP7603884A JPS60219094A JP S60219094 A JPS60219094 A JP S60219094A JP 59076038 A JP59076038 A JP 59076038A JP 7603884 A JP7603884 A JP 7603884A JP S60219094 A JPS60219094 A JP S60219094A
Authority
JP
Japan
Prior art keywords
composition layer
layer
fine powder
fine particles
polymer composition
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
JP59076038A
Other languages
Japanese (ja)
Other versions
JPH0630974B2 (en
Inventor
Akihiro Imai
章博 今井
Tokihiko Shimizu
清水 時彦
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 JP59076038A priority Critical patent/JPH0630974B2/en
Priority to CA000464122A priority patent/CA1228728A/en
Priority to DE8484306649T priority patent/DE3482459D1/en
Priority to EP84306649A priority patent/EP0138483B1/en
Publication of JPS60219094A publication Critical patent/JPS60219094A/en
Priority to US06/910,832 priority patent/US4684561A/en
Publication of JPH0630974B2 publication Critical patent/JPH0630974B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • B41M5/40Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42Intermediate, backcoat, or covering layers
    • 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
    • B41M5/40Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/405Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography characterised by layers cured by radiation
    • 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
    • B41M5/40Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42Intermediate, backcoat, or covering layers
    • B41M5/44Intermediate, backcoat, or covering layers characterised by the macromolecular compounds
    • B41M5/443Silicon-containing polymers, e.g. silicones, siloxanes
    • 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
    • B41M5/40Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42Intermediate, backcoat, or covering layers
    • B41M5/423Intermediate, backcoat, or covering layers characterised by non-macromolecular compounds, e.g. waxes
    • 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
    • B41M5/40Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42Intermediate, backcoat, or covering layers
    • B41M5/426Intermediate, backcoat, or covering layers characterised by inorganic compounds, e.g. metals, metal salts, metal complexes
    • 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
    • B41M5/40Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42Intermediate, backcoat, or covering layers
    • B41M5/44Intermediate, backcoat, or covering layers characterised by the macromolecular compounds

Landscapes

  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Impression-Transfer Materials And Handling Thereof (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)

Abstract

PURPOSE:To provide the titled transfer material free of dropout in images and free of sticking, wherein a coloring material layer is provided on the upper side of a film form base, and a polymeric composition layer comprising a fine powder, a surface active agent and a polymeric substance is provided on the lower side of the base so that the surface of the composition layer is roughened by the fine powder. CONSTITUTION:The coloring material layer (comprising a pigment, a dye and a color former) 5 is provided on the upper side of the film form base (e.g., a polyethylene terephthalate film) 4, and the polymeric composition layer 6 comprising a fine powder (e.g., synthetic amorphous silica) 7, a surface active agent (e.g., a cationic surface active agent) 8 and a polymeric substance (e.g., a silicone resin), optionally with a liquid lubricant (e.g., dimethyl polysiloxane) or a solid lubricant (e.g., stearyl alcohol) is provided on the lower side of the base 4 so that the fine powder 7 is not only present in the inside part of the layer 6 but exposed to the surface of the layer 6, to obtain the desired transfer material.

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r、れる感熱記録用
転写体に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a transfer body for thermal recording used for recording by thermal transfer.

従来例の構成とその問題点 感熱記録用転写体(以下、転写体と略す)の概略断面図
を第1図((示す。1は転写体の基体、2はその上に形
成された色材層、3は高分子組成物層である。
A schematic cross-sectional view of a transfer body for heat-sensitive recording (hereinafter referred to as the transfer body) is shown in FIG. Layer 3 is a polymer composition layer.

ポリエチレンテレフタレート(以下、PETと略す)等
の高分子フィルムを基体1に用いた場合、サーマルヘッ
ドの熱パルスによる基体の熱溶融あるいは走行時に発生
する静電気により基体がサーマルヘッドに付着するいわ
ゆるスティック現象が発生する。その結果、基体がサー
マルヘッド上を安定に走行しない。
When a polymer film such as polyethylene terephthalate (hereinafter abbreviated as PET) is used as the substrate 1, the so-called stick phenomenon occurs in which the substrate adheres to the thermal head due to thermal melting of the substrate due to the heat pulse of the thermal head or static electricity generated during running. Occur. As a result, the base body does not run stably on the thermal head.

そのため、基体の下面に側熱性保護膜を設ける(特開昭
56−746’ 7号公報)、滑性の高い無機顔料と熱
硬化外寸たけ高軟化点の樹脂材料とからなるスティック
防止層を設ける(特開昭66−155794号公報)、
常温で固体ないし半固体の界面活性剤または有機塩類を
含有する樹脂層を設ける(特開昭57−129789号
公報)等の提案がなされている。
Therefore, a heat-resistant protective film is provided on the lower surface of the substrate (Japanese Unexamined Patent Publication No. 56-746'7), and a stick prevention layer made of a highly slippery inorganic pigment and a thermosetting resin material with a high softening point and external dimension is used. (Japanese Unexamined Patent Publication No. 155794/1983)
Proposals have been made to provide a resin layer containing a surfactant or an organic salt that is solid or semi-solid at room temperature (Japanese Patent Application Laid-open No. 129789/1989).

しかし、スティックに対する上記のような種々ラテンと
サーマルヘッドの抑圧の不均一な所で特に高分子材料あ
るいは添加剤が削られてきて発熱体上にたまり画像にプ
リント抜け(ドロップアウト)が生じるという問題が発
生した。
However, there is a problem in that the polymeric material or additives are scraped off and accumulated on the heating element due to uneven pressure of the various latin and thermal heads on the stick as described above, resulting in dropouts in the image. There has occurred.

発明の目的 本発明は、上記のような従来の欠点を解消し、画像にド
ロップアウトがなく、かつスティックしない転写体を提
供することを目的とする。
OBJECTS OF THE INVENTION It is an object of the present invention to eliminate the above-mentioned conventional drawbacks and to provide a transfer member that does not cause image dropouts and does not stick.

発明の構成 本発明によれば基体の下面に、微粒子と界面活性剤と高
分子物質からなる高分子組成物層が設けられ、かつその
微粒子により高分子組成物層の表面が粗面化されている
Structure of the Invention According to the present invention, a polymer composition layer made of fine particles, a surfactant, and a polymer substance is provided on the lower surface of a substrate, and the surface of the polymer composition layer is roughened by the fine particles. There is.

又、必要に応じて前記の高分子組成物層にさらに液体滑
剤、あるいは固体滑剤、あるいは液体滑剤と固体滑剤の
両方が添加される。
Further, if necessary, a liquid lubricant, a solid lubricant, or both a liquid lubricant and a solid lubricant may be added to the polymer composition layer.

界面活性剤はスティックを防止するため、微粒子はドロ
ップアウトを防止するだめの機能を果す。
Since the surfactant prevents sticking, the particulates act as a barrier to prevent dropout.

す々わち、微粒子を添加することにより粗面化された高
分子組成物層の表面がヘッド上の鋭い凹凸を吸ミカ 収するため、発熱体上に堆積物を発生せずン話果、ドロ
ップアウトの発生を防止できるので、界面活性剤による
スティック防止効果を十分に活かすことができる。
In other words, the surface of the polymer composition layer, which has been roughened by adding fine particles, absorbs the sharp unevenness on the head, so no deposits are generated on the heating element. Since the occurrence of dropout can be prevented, the stick prevention effect of the surfactant can be fully utilized.

又、スティックは界面活性剤と液体滑剤、あるいは界面
活性剤と固体滑剤、あるいは界面活性剤と液体滑剤と固
体滑剤とを組み合わせて用いることにより、更に有効に
防止される。
In addition, stickiness can be more effectively prevented by using a combination of a surfactant and a liquid lubricant, a surfactant and a solid lubricant, or a combination of a surfactant, a liquid lubricant, and a solid lubricant.

実施例の説明 以下、本発明の実施例について説明する。Description of examples Examples of the present invention will be described below.

本発明の実施例として転写体の概略断面図を第2図に示
す。基体4の上面に色材層5があり、下面に高分子組成
物層6がある。高分子組成物層6は微粒子7゛、界面活
性剤8.高分子物質から構成されている。微粒子7は高
分子組成物層6の内部だけでなく表面にも露出するよう
含有されている。
FIG. 2 shows a schematic cross-sectional view of a transfer body as an embodiment of the present invention. A coloring material layer 5 is provided on the upper surface of the substrate 4, and a polymer composition layer 6 is provided on the lower surface. The polymer composition layer 6 includes fine particles 7, surfactant 8. It is composed of polymeric substances. The fine particles 7 are contained so as to be exposed not only inside the polymer composition layer 6 but also on the surface thereof.

高分子組成物層6には、さらに必要に応じて、液体滑剤
、あるいは固体滑剤、あるいは液体滑剤と固体滑剤の両
方を含有させることも効果的である。
It is also effective for the polymer composition layer 6 to further contain a liquid lubricant, a solid lubricant, or both a liquid lubricant and a solid lubricant, if necessary.

微粒子の材質は、特に限定されるものではなく、金属、
無機系、有機系の各種粒子を用いることができる。例え
ば、金属酸化物、金属硫化物、金属炭化物、金属窒化物
、金属フッ化物、黒鉛、フッ子等がある。
The material of the fine particles is not particularly limited, and may include metal,
Various inorganic and organic particles can be used. Examples include metal oxides, metal sulfides, metal carbides, metal nitrides, metal fluorides, graphite, fluoride, and the like.

特に合成非晶質シリカ、カーボンブラック、アルミナ、
酸化チタン、珪酸カルシウム、珪酸アルミニウム等が有
力である。
Especially synthetic amorphous silica, carbon black, alumina,
Titanium oxide, calcium silicate, aluminum silicate, etc. are promising.

合成非晶質シリカには無水シリカ及び含水ノリ力がある
。無水シリカとしては気相法で作製された超微粒子が有
用である。例えば、西独デグサ社で開発された高純度の
超微粒子状シリカ(商品名:アエロジル2日本ア臣ロジ
ル株式会社)、同様に気相法で作製された酸化アルミニ
ウム、酸化チタン(いずれも、日本アエロジル株式会社
)等がある。
Synthetic amorphous silica has anhydrous silica and hydrous adhesive properties. As the anhydrous silica, ultrafine particles produced by a gas phase method are useful. For example, high-purity ultrafine particulate silica (product name: Aerosil 2 Nippon Ashin Rosil Co., Ltd.) developed by West German Degussa, aluminum oxide and titanium oxide (both Nippon Aerosil Ltd.) etc.

含水シリカあるいはホワイトカーボンとして、例えば、
塩野義製薬株式会社「カープレックス」。
As hydrated silica or white carbon, for example,
Shionogi & Co., Ltd. “Carplex”.

日本7リカエ業株式会社「ニップノール」、水澤化学工
業株式会社「シルト/」、徳山曹達株式会社「ファイン
ンール、トクノール」等か市販されている。
Nippon 7 Rikae Gyo Co., Ltd.'s ``Nipnol'', Mizusawa Chemical Industry Co., Ltd.'s ``Silt/'', Tokuyama Soda Co., Ltd.'s ``Finenol, Tokunor'', etc. are commercially available.

シリカは、使用する染料の特性によっては染料と反応す
る場合もあるため、シリカに存在するンラノール基を化
学的にメチル基あるいは有機珪素化合物等で一部置換結
合させた疎水性シリカを用いることかできる。
Since silica may react with dyes depending on the characteristics of the dye used, it is recommended to use hydrophobic silica in which the lanol groups present in silica are chemically bonded by partial substitution with methyl groups or organic silicon compounds. can.

微粒子の高分子物質に対する添加比率は0.1〜200
重量係の範囲で用いることができる。特に添加比率が5
〜100重量係の範囲で安定した特性を示す。超微粒子
は、超音波、三本ロール、ホモジナイザー等によりよく
分散される。
The addition ratio of fine particles to polymeric substance is 0.1 to 200.
Can be used within the weight range. Especially when the addition ratio is 5
It shows stable characteristics in the range of ~100 weight coefficient. Ultrafine particles are well dispersed by ultrasonic waves, triple rolls, homogenizers, and the like.

微粒子の大きさは、その粒径が小さい程画質への影響が
少なく、特に平均粒径が6μm以下の場合にドロップア
ウトがほとんど生じなくなるので望ましい。
Regarding the size of the fine particles, it is preferable that the smaller the particle size, the less the influence on the image quality, and especially when the average particle size is 6 μm or less, dropout hardly occurs.

高分子物質としてはその材質を特に限定されるものでな
く、例えば、各種熱可塑性樹脂、熱、光。
There are no particular limitations on the material used for the polymeric substance, such as various thermoplastic resins, heat, and light.

電子線等による各種硬化性樹脂の硬化樹脂等を用いるこ
とができる。特に各種硬化性樹脂が基体との接着性およ
び耐熱性において良好である。
Various types of curable resins cured by electron beam or the like can be used. In particular, various curable resins have good adhesion to the substrate and heat resistance.

例えば、シリコーン樹脂、エポキシ樹脂、不飽和アルデ
ヒド樹脂、ユリア樹脂、不飽和ポリエステル樹脂、アル
キド樹脂、フラン樹脂、オリゴアクリレート等がある。
Examples include silicone resins, epoxy resins, unsaturated aldehyde resins, urea resins, unsaturated polyester resins, alkyd resins, furan resins, oligoacrylates, and the like.

中でもオリゴアクリレートの硬化樹脂が優れた特性を示
す。又、光、電子線による硬化樹脂が矧時間で容易に硬
化し、又、基材裏面への未反応樹脂、硬化剤等の転移が
ほとんどないため、長尺の転写体を作製しやすく、又、
良好な特性を示す。
Among these, oligoacrylate cured resins exhibit excellent properties. In addition, the resin cured by light or electron beams is easily cured in a short period of time, and there is almost no transfer of unreacted resin, curing agent, etc. to the back surface of the base material, making it easy to produce long transfer bodies. ,
Shows good properties.

例えば、オリゴアクリレートの光、あるいは電子線硬化
樹脂、あるいは芳香族ジアゾニウム塩、あるいは芳香族
ヨードニウム塩、あるいは芳香族スルホニウム塩触媒に
よるエポキシ樹脂の光硬化樹脂が優れている。
For example, light- or electron beam-curable resins of oligoacrylates, or photo-curable resins of epoxy resins catalyzed by aromatic diazonium salts, aromatic iodonium salts, or aromatic sulfonium salts are excellent.

オリゴアクリレートとしては、例えば、ポリオールアク
リレート−ポリエステルアクリレート。
As the oligoacrylate, for example, polyol acrylate-polyester acrylate.

エポキシアクリレート、ウレタンアクリレート。Epoxy acrylate, urethane acrylate.

シリコーンアクリレート、ポリアセクールのアクリレー
ト等、 エポキシ樹脂としては、例えば、ビニルシクロヘキセン
ジオキシト、3.4−エポキ/シクロヘキシルメチル−
3,4−エポキシシクロヘキサンカルボキシレイト等の
環状脂肪族エポキシ樹脂がある。
Silicone acrylate, polyacecool acrylate, etc. Epoxy resins include, for example, vinylcyclohexene dioxide, 3,4-epoxy/cyclohexylmethyl-
There are cycloaliphatic epoxy resins such as 3,4-epoxycyclohexane carboxylate.

又、テトラヒドロフルフリルアクリレート、ラウリルア
クリレート等の反応性希釈剤を樹脂に添加して用いるこ
ともできる8 高分子組成物の膜厚は特に限定されるものでない。一般
に製造面から0.1μm以上の膜厚を有する高分子組成
物か得やすく均一な特性を示す。
Furthermore, a reactive diluent such as tetrahydrofurfuryl acrylate or lauryl acrylate may be added to the resin.8 The film thickness of the polymer composition is not particularly limited. Generally, from the manufacturing point of view, polymer compositions having a film thickness of 0.1 μm or more are easy to obtain and exhibit uniform properties.

界面活性剤としては、従来からよく知られている各種界
面活性剤を用いることができる。
As the surfactant, various conventionally well-known surfactants can be used.

例えば、カルボン酸塩、スルホン酸塩、硫酸エステル塩
、リン酸エステル塩等の各種陰イオン界面活性剤、 各種脂肪族アミン塩、脂肪族4級アンモニウム塩、芳香
族4級アンモニウム塩、複素環4級アンモニウム塩等の
各種陽イオン界面活性剤、ポリオキシエチレンアルキル
エーテル、ポリオキシエチレンアルキルフェニルニー7
− /l/ 等(7) x −チル型、ポリオキシエチ
レングリセリン脂肪酸エステル、ポリオキシエチレンソ
ルビクン脂肪酸エステル等のエーテルエステル型、ポリ
エチレングリコール脂肪酸エステル、脂肪酸モノグリセ
リド。
For example, various anionic surfactants such as carboxylates, sulfonates, sulfate ester salts, phosphate ester salts, various aliphatic amine salts, aliphatic quaternary ammonium salts, aromatic quaternary ammonium salts, heterocyclic 4 various cationic surfactants such as ammonium salts, polyoxyethylene alkyl ether, polyoxyethylene alkyl phenyl 7
- /l/ etc. (7) x -chill type, ether ester type such as polyoxyethylene glycerin fatty acid ester, polyoxyethylene sorbicun fatty acid ester, polyethylene glycol fatty acid ester, fatty acid monoglyceride.

ソルビタン脂肪酸エステル、プロピレングリコール脂肪
酸エステル、シボ糖脂肪酸エステル等のエステル型、脂
肪酸アルカノールアミド、ポリオキシエチレン脂肪酸ア
ミド、ポリオキシエチレンアルキルアミン、アルキルア
ミンオキザイド等の含窒素型等の各種非イオン界面活性
剤、 各種ベタイン型、アミノカルボン酸塩型、イミダシリン
誘導体等の各種両性界面活性剤、フルオロアルキル(C
2〜C2o)カルボン酸、モノパーフルオロアルキル(
06〜C16)エチルリン酸エステル、パーフルオロオ
クタンスルフAン酸ジェタノールアミド等の各種フッソ
系界面活性剤。
Various nonionic surfactants such as ester types such as sorbitan fatty acid ester, propylene glycol fatty acid ester, and cibosugar fatty acid ester, and nitrogen-containing types such as fatty acid alkanolamide, polyoxyethylene fatty acid amide, polyoxyethylene alkylamine, and alkylamine oxide. various betaine type, aminocarboxylate type, various amphoteric surfactants such as imidacillin derivatives, fluoroalkyl (C
2-C2o) carboxylic acid, monoperfluoroalkyl (
06-C16) Various fluorosurfactants such as ethyl phosphate and perfluorooctane sulfanoic acid jetanolamide.

ポリエーテル変性シリコーンオイル、カルボキシル変性
ノリコーンオイル、アルキルアラルキルポリエーテル変
性シリコーンオイル、エポキシΦポリエーテル変性〆リ
コーンオイル等の各種変性シリコーンオイル、ポリオキ
シアルキレングリコールとシリコーンとの各種共重合体
等の各種シリコーン系界面活性剤がある。
Various modified silicone oils such as polyether modified silicone oil, carboxyl modified silicone oil, alkyl aralkyl polyether modified silicone oil, epoxy Φ polyether modified silicone oil, various copolymers of polyoxyalkylene glycol and silicone, etc. There are silicone surfactants.

さらに、高分子界面活性剤、有機金属界面活性剤9反応
性界面活性剤等と称される界面活性剤も本発明に用いる
ことができる。
Furthermore, surfactants called polymeric surfactants, organometallic surfactants, 9-reactive surfactants, and the like can also be used in the present invention.

ノリコーン系、フッソ系界面活性剤が特に優れており、
上記界面活性剤とシリコーン系、フッソ系界面活性剤を
併用して用いるとステー(ンク防止に対する効果が優れ
ている。又、HLB値が3.0以下と3−0以上、ある
いはHLB値の値が3以上離れている界面活性剤を2つ
以上併用して用いるとその効果が著しい。
Noricone-based and fluoro-based surfactants are particularly excellent.
When the above-mentioned surfactants are used in combination with silicone-based or fluoro-based surfactants, the effect on preventing staining is excellent. The effect is remarkable when two or more surfactants with a distance of 3 or more are used in combination.

液体滑剤は26℃、1気圧において液体であり、潤滑性
を示す物質である。
A liquid lubricant is a substance that is liquid at 26° C. and 1 atm and exhibits lubricating properties.

例えば、ジメチルポリシロキサン、メチルフェニルポリ
シロキサン、メチルハイドロジエンポリシロキサン、フ
ッソシリコーンオイル等のシリコーン系オイル、 アルキルベンゼン、ポリブテン、アルキルナフタレン、
アルキルジフェニルエタン、リン酸エステル等の合成油
、 飽和炭化水素、動植物油、鉱物油、エチレングリコール
、プロピレングリコール、ポリアルキレングリコール等
のグリコール類、グリセリン及びグリセリン誘導体、ブ
チルステアレート等のエステル類、流動パラフィン等が
ある。
For example, silicone oils such as dimethylpolysiloxane, methylphenylpolysiloxane, methylhydrodienepolysiloxane, fluorosilicone oil, alkylbenzenes, polybutenes, alkylnaphthalenes,
Synthetic oils such as alkyldiphenylethanes and phosphoric acid esters, saturated hydrocarbons, animal and vegetable oils, mineral oils, glycols such as ethylene glycol, propylene glycol, and polyalkylene glycols, glycerin and glycerin derivatives, esters such as butyl stearate, fluids There are paraffin etc.

固体滑剤は、25℃、1気圧において、固体あるいは半
固体の滑剤である。例えば、ステアリルアルコール、マ
ンニトール等の各種アルコール。
A solid lubricant is a lubricant that is solid or semi-solid at 25° C. and 1 atmosphere. For example, various alcohols such as stearyl alcohol and mannitol.

ステアリン酸、モンタン酸等の脂肪酸、ステアリルステ
アレート、セチルパルミテート、ペンタエリスリトール
テトラステアレート等の脂肪酸エステル、マイクロクリ
スタリンワックス、ポリオレフィンワックス等のワック
ス類、およびこれらの部分酸化物、、ワラ化物、塩化物
等の脂肪族炭化水素、バルミチン酸アミド、エチレンビ
スステア 1)ン酸アミド等の脂肪酸アミド、 ステアリン酸カルシウム、ステアリン酸アルミニウム等
の金属石けん、 黒鉛、二硫化モリブデン、四フッ化エチレン。
Fatty acids such as stearic acid and montanic acid, fatty acid esters such as stearyl stearate, cetyl palmitate, and pentaerythritol tetrastearate, waxes such as microcrystalline wax and polyolefin wax, and their partial oxides, straw, and chloride. aliphatic hydrocarbons such as balmitic acid amide, ethylene bisstearate, etc. 1) Fatty acid amides such as nitric acid amide, metal soaps such as calcium stearate and aluminum stearate, graphite, molybdenum disulfide, and ethylene tetrafluoride.

フッ化カーボン、タルク等がある。Carbon fluoride, talc, etc.

本発明において用いる基体は、高分子フィルムであれば
特に限定されるものでなく、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、セロハン等の士ルロース誘導
体、ポリ7ノ化ビニリデン、47ノ化エチレン−6ツノ
化プロピレン共重合体、テフロン等のフッソ系高分子、
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ィン系高分子、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。
The substrate used in the present invention is not particularly limited as long as it is a polymer film, and examples include ester polymers such as polyethylene terephthalate, polyethylene naphthalate, and polycarbonate, amide polymers such as nylon, acetyl cellulose, and cellophane. fluorine-based polymers such as polyvinylidene heptanoide, 47-oxyethylene-hexapropylene copolymer, Teflon, etc.
Ether polymers such as polyoxymethylene and polyacetal, polystyrene, polyethylene, polypropylene,
Olefin polymers such as methylpentene polymers, imide polymers such as polyimide, polyamideimide, polyetherimide, etc. can be used.

特に、ポリエステル系高分子は薄く、ある程度の耐熱性
もあり、安価であるので有用である。
In particular, polyester polymers are useful because they are thin, have a certain degree of heat resistance, and are inexpensive.

又、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基体とし
て有用である。
In addition, imide-based polymers, which are more heat resistant than polyester-based polymers,
For polymers such as amide-based polymers, when using the transfer material repeatedly,
It is useful as a substrate because it has excellent heat resistance when used at high speeds.

色材層は特に限定されるものでなくワ、ノクス方式、昇
華染料方式等で用いられている各種電制層構成を用いる
ことができる。色材は顔料、染料のほかにカラーフォー
マ−も含む。昇華性染料としては、30Q℃以下で昇華
あるいは蒸発を始める染料を用いることができ、例えば
、塩基性染料。
The coloring material layer is not particularly limited, and various electrostatic layer configurations used in the Wax, Nox method, sublimation dye method, etc. can be used. Color materials include pigments, dyes, and color formers. As the sublimable dye, a dye that starts to sublimate or evaporate at 30Q°C or lower can be used, such as a basic dye.

分散染料等がある。There are disperse dyes, etc.

以下、さらに具体的に説明する。This will be explained in more detail below.

実施例1 基体に厚さ12μmのPETフィルムを用いた。Example 1 A PET film with a thickness of 12 μm was used as the substrate.

第1表に示した組成からなる各塗布液(蒲1〜&4)を
作製した。
Each coating liquid (Pump 1 to &4) having the composition shown in Table 1 was prepared.

PETフィルムの下面に爲1塗布液をワイヤーバーで塗
布し、60℃の熱風で溶媒を蒸発させた後、1KWの高
圧水銀灯を照射して硬化させた。
Coating solution No. 1 was applied to the lower surface of the PET film using a wire bar, the solvent was evaporated with hot air at 60° C., and then cured by irradiation with a 1 KW high-pressure mercury lamp.

爲2〜爲4の各塗布液についても同様に行い、下面に高
分子組成物層を有するPETフィルムを得た。
The same procedure was applied to each of the coating solutions No. 2 to No. 4 to obtain a PET film having a polymer composition layer on the lower surface.

次に下記の分子構造で表わされる昇華性染料2重量部、
ポリカーボネート4重量部、塩化メチレン100重量部
を混合したインキを上記のように加工したPETフィル
ムの上面にワイヤーノぐ−で塗λ0した後60℃の熱風
で乾燥させ4種類の転写体を作製した。
Next, 2 parts by weight of a sublimable dye represented by the following molecular structure,
An ink mixture of 4 parts by weight of polycarbonate and 100 parts by weight of methylene chloride was coated with a wire glue on the top surface of the PET film processed as described above at λ0, and then dried with hot air at 60°C to produce four types of transfer bodies. .

この各転写体を用いて、以下の薄膜型サーマルヘッド記
録条件で、A−5版の活性クレーコート紙上に記録を行
った。
Using each of the transfer bodies, recording was carried out on A-5 plate activated clay coated paper under the following thin-film thermal head recording conditions.

主および副走査の線密度=4ドツト/ mm記録電力 
:0.7W/ドツト ヘツドの加熱時間 :2〜8m5 1ラインの記録時間 : 33 、’s ms記録面積
 :A−6版 この試験結果を第1表に示す。本発明に係る塗布液LI
 r &2は8mBにおいてもスティックを発生せず、
かつドロップアウトの発生も皆無であった。一方、比較
例筋3は3msでスティックして転写体が溶融切断した
だめ、ドロップアウトの評価は不可能であった。又、比
較例f。4は画像に白線(プリントされない部分)を生
じるドロップアウト、をA−5版1枚目で発生した。
Linear density of main and sub-scanning = 4 dots/mm Recording power
Heating time of 0.7 W/dot head: 2 to 8 m5 Recording time of one line: 33,'s ms Recording area: A-6 version The results of this test are shown in Table 1. Coating liquid LI according to the present invention
r &2 does not generate stick even at 8mB,
Moreover, there were no occurrences of dropouts. On the other hand, Comparative Example 3 stuck for 3 ms and the transfer body was melted and cut, so it was impossible to evaluate dropout. Also, comparative example f. In No. 4, dropout, which causes white lines (unprinted areas) in the image, occurred on the first sheet of A-5 size.

以下余白 実施例2 基体に厚さ9μmのPETフィルムを用いた。Margin below Example 2 A PET film with a thickness of 9 μm was used as the substrate.

第2表に示した各塗布液において、溶媒と増感剤以外に
、爲1は微粒子、液体滑剤、界面活性剤と高分子物質を
含み、爲2は微粒子、固体滑剤、界面活性剤と高分子物
質を含み、爲3は微粒子、液体滑材、固体滑剤、界面活
性剤と高分子物質を含む。以下、実施例1と同様にして
、基体の下面に上記各塗布液から高分子組成物層を形成
し、上面に色材層を形成して、3種類の転写体を作製し
た後、ステインク及びドロップアウトの発生試験を、ヘ
ッドに加える記録電力を0.77Wに上げて行なった。
In each coating solution shown in Table 2, in addition to the solvent and sensitizer, 1 contains fine particles, a liquid lubricant, a surfactant, and a polymeric substance, and 2 contains fine particles, a solid lubricant, a surfactant, and a polymeric substance. Contains molecular substances, including fine particles, liquid lubricants, solid lubricants, surfactants and polymer substances. Thereafter, in the same manner as in Example 1, a polymer composition layer was formed from each of the above coating liquids on the lower surface of the substrate, and a coloring material layer was formed on the upper surface to prepare three types of transfer bodies. A dropout occurrence test was conducted by increasing the recording power applied to the head to 0.77W.

この試験結果を第2表に示す。本発明に係る塗布Wi、
L 1− tK 3は0.77 ’W 、 8 msに
お・いてもスティックを発生せず、かつドロップアウト
の発生も皆無であった。
The test results are shown in Table 2. Coating Wi according to the present invention,
L1-tK3 did not cause stick even at 0.77'W and 8 ms, and no dropout occurred.

以下余白 発明の効果 以上のように本発明の転写体は、画像に1つたくドロッ
プアウトがなく、かつスティックしないため、高品質で
安価な画像を多数提供することができ、さらに高速記録
にも利用できる。
Effects of the Margin Invention As described above, the transfer body of the present invention has no dropouts and does not stick to images, so it can provide a large number of high-quality and inexpensive images, and can also be used for high-speed recording. Available.

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

第1図は従来の感熱記録用転写体の断面図、第2図は本
発明の一実施例における感熱記録用転写体の概略断面図
である。 4 ・・・・基体、5・・・・色材層、6・・・・・高
分子組成物層、7・・・・・・微粒子、8・・・・・・
界面活性剤。 代理人の氏名 弁理士 中 尾 敏 男 ほか1名第1
FIG. 1 is a sectional view of a conventional transfer body for thermal recording, and FIG. 2 is a schematic sectional view of a transfer body for thermal recording according to an embodiment of the present invention. 4...Substrate, 5...Coloring material layer, 6...Polymer composition layer, 7...Fine particles, 8...
surfactant. Name of agent: Patent attorney Toshio Nakao and 1 other person No. 1
figure

Claims (4)

【特許請求の範囲】[Claims] (1) フィルム状の基体の上面に色材層が設けられ、
前記基体の下面に微粒子と界面活性剤と高分子物質とを
含む高分子組成物層が設けられ、かつ前記微粒子により
前記高分子組成物層の表面が粗面化されている感熱記録
用転写体。
(1) A coloring material layer is provided on the top surface of a film-like substrate,
A transfer body for thermal recording, wherein a polymer composition layer containing fine particles, a surfactant, and a polymer substance is provided on the lower surface of the substrate, and the surface of the polymer composition layer is roughened by the fine particles. .
(2)高分子組成物層が微粒子と液体滑剤と界面活性剤
と高分子物質からなる特許請求の範囲第1項記載の感熱
記録用転写体。
(2) A transfer body for thermal recording according to claim 1, wherein the polymer composition layer comprises fine particles, a liquid lubricant, a surfactant, and a polymer substance.
(3)高分子組成物層が微粒子と固体滑剤と界面活性剤
と高分子物質からなる特許請求の範囲第1項記載の感熱
記録用転写体。
(3) A transfer body for thermal recording according to claim 1, wherein the polymer composition layer comprises fine particles, a solid lubricant, a surfactant, and a polymer substance.
(4)高分子組成物層が微粒子と液体滑剤と固体滑剤と
界面活性剤と高分子物質からなる特許請求の範囲第1項
記載の感熱記録用転写体。
(4) A transfer body for thermal recording according to claim 1, wherein the polymer composition layer comprises fine particles, a liquid lubricant, a solid lubricant, a surfactant, and a polymer substance.
JP59076038A 1983-09-28 1984-04-16 Transfer material for thermal recording Expired - Lifetime JPH0630974B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP59076038A JPH0630974B2 (en) 1984-04-16 1984-04-16 Transfer material for thermal recording
CA000464122A CA1228728A (en) 1983-09-28 1984-09-27 Color sheets for thermal transfer printing
DE8484306649T DE3482459D1 (en) 1983-09-28 1984-09-28 COLOR LAYERS FOR HEAT TRANSFER PRINTING.
EP84306649A EP0138483B1 (en) 1983-09-28 1984-09-28 Color sheets for thermal transfer printing
US06/910,832 US4684561A (en) 1983-09-28 1986-09-23 Color sheets for thermal transfer printing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59076038A JPH0630974B2 (en) 1984-04-16 1984-04-16 Transfer material for thermal recording

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP7009008A Division JP2538196B2 (en) 1995-01-24 1995-01-24 Transferr for thermal recording

Publications (2)

Publication Number Publication Date
JPS60219094A true JPS60219094A (en) 1985-11-01
JPH0630974B2 JPH0630974B2 (en) 1994-04-27

Family

ID=13593634

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59076038A Expired - Lifetime JPH0630974B2 (en) 1983-09-28 1984-04-16 Transfer material for thermal recording

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Country Link
JP (1) JPH0630974B2 (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61175089A (en) * 1985-01-31 1986-08-06 Dainippon Printing Co Ltd Thermal transfer sheet
JPS62191188A (en) * 1985-12-24 1987-08-21 イ−ストマン コダック カンパニ− Lubricant slipping layer for dyestuff-donor member used for heat transfer dyestuff
JPS62191189A (en) * 1985-12-24 1987-08-21 イ−ストマン・コダック・カンパニ− Slipping layer for pigment dative element used for pigment heat transfer
JPS62286789A (en) * 1986-06-05 1987-12-12 Hitachi Maxell Ltd Thermal transfer recording material
JPS62286788A (en) * 1986-06-05 1987-12-12 Hitachi Maxell Ltd Thermal transfer recording material
JPS62290581A (en) * 1986-06-09 1987-12-17 Mitsubishi Paper Mills Ltd Heat transfer recording material
JPS62292484A (en) * 1986-06-11 1987-12-19 Diafoil Co Ltd Thermal transfer film
JPS6398484A (en) * 1986-10-15 1988-04-28 Toray Ind Inc Transfer material for thermal recording
JPS63194982A (en) * 1987-02-09 1988-08-12 Dainippon Printing Co Ltd Thermal transfer sheet for forming transparent copy
JPS63222892A (en) * 1987-03-12 1988-09-16 Mitsubishi Paper Mills Ltd Thermal transfer material
JPS63170251U (en) * 1987-04-25 1988-11-07
JPS641586A (en) * 1987-03-02 1989-01-05 Konica Corp Thermal transfer recording medium
JPS6487295A (en) * 1987-06-16 1989-03-31 Eastman Kodak Co Solid grain lubricant for sliding layer of dye dative element used for heat transfer of dye
JPH01234292A (en) * 1988-03-15 1989-09-19 Toppan Printing Co Ltd Thermal transfer recording medium
JPH01241491A (en) * 1988-03-23 1989-09-26 Mitsubishi Kasei Corp Image-receiving material for thermal transfer recording
JP2014058071A (en) * 2012-09-14 2014-04-03 Dainippon Printing Co Ltd Thermal transfer sheet
JP2014058070A (en) * 2012-09-14 2014-04-03 Dainippon Printing Co Ltd Thermal transfer sheet

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56155794A (en) * 1980-05-06 1981-12-02 Fuji Kagaku Kogyo Kk Thermo-sensitive transfer material
JPS57129789A (en) * 1981-02-05 1982-08-11 Fuji Kagakushi Kogyo Co Ltd Heat sensitive transferring material
JPS58101095A (en) * 1981-12-12 1983-06-16 Fuji Kagakushi Kogyo Co Ltd Heat transfer recording medium
JPS58171992A (en) * 1982-04-01 1983-10-08 Dainippon Printing Co Ltd Heat sensitive transfer sheet
JPS58187396A (en) * 1982-04-27 1983-11-01 Dainippon Printing Co Ltd Heat-sensitive transfer sheet

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56155794A (en) * 1980-05-06 1981-12-02 Fuji Kagaku Kogyo Kk Thermo-sensitive transfer material
JPS57129789A (en) * 1981-02-05 1982-08-11 Fuji Kagakushi Kogyo Co Ltd Heat sensitive transferring material
JPS58101095A (en) * 1981-12-12 1983-06-16 Fuji Kagakushi Kogyo Co Ltd Heat transfer recording medium
JPS58171992A (en) * 1982-04-01 1983-10-08 Dainippon Printing Co Ltd Heat sensitive transfer sheet
JPS58187396A (en) * 1982-04-27 1983-11-01 Dainippon Printing Co Ltd Heat-sensitive transfer sheet

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61175089A (en) * 1985-01-31 1986-08-06 Dainippon Printing Co Ltd Thermal transfer sheet
JPH0460438B2 (en) * 1985-12-24 1992-09-28 Eastman Kodak Co
JPS62191188A (en) * 1985-12-24 1987-08-21 イ−ストマン コダック カンパニ− Lubricant slipping layer for dyestuff-donor member used for heat transfer dyestuff
JPS62191189A (en) * 1985-12-24 1987-08-21 イ−ストマン・コダック・カンパニ− Slipping layer for pigment dative element used for pigment heat transfer
JPH0466196B2 (en) * 1985-12-24 1992-10-22 Eastman Kodak Co
JPS62286789A (en) * 1986-06-05 1987-12-12 Hitachi Maxell Ltd Thermal transfer recording material
JPS62286788A (en) * 1986-06-05 1987-12-12 Hitachi Maxell Ltd Thermal transfer recording material
JPS62290581A (en) * 1986-06-09 1987-12-17 Mitsubishi Paper Mills Ltd Heat transfer recording material
JPH0519917B2 (en) * 1986-06-09 1993-03-18 Mitsubishi Paper Mills Ltd
JPH0560438B2 (en) * 1986-06-11 1993-09-02 Diafoil Hoechst Co Ltd
JPS62292484A (en) * 1986-06-11 1987-12-19 Diafoil Co Ltd Thermal transfer film
JPS6398484A (en) * 1986-10-15 1988-04-28 Toray Ind Inc Transfer material for thermal recording
JPS63194982A (en) * 1987-02-09 1988-08-12 Dainippon Printing Co Ltd Thermal transfer sheet for forming transparent copy
JPS641586A (en) * 1987-03-02 1989-01-05 Konica Corp Thermal transfer recording medium
JPS63222892A (en) * 1987-03-12 1988-09-16 Mitsubishi Paper Mills Ltd Thermal transfer material
JPS63170251U (en) * 1987-04-25 1988-11-07
JPS6487295A (en) * 1987-06-16 1989-03-31 Eastman Kodak Co Solid grain lubricant for sliding layer of dye dative element used for heat transfer of dye
JPH01234292A (en) * 1988-03-15 1989-09-19 Toppan Printing Co Ltd Thermal transfer recording medium
JPH01241491A (en) * 1988-03-23 1989-09-26 Mitsubishi Kasei Corp Image-receiving material for thermal transfer recording
JP2014058071A (en) * 2012-09-14 2014-04-03 Dainippon Printing Co Ltd Thermal transfer sheet
JP2014058070A (en) * 2012-09-14 2014-04-03 Dainippon Printing Co Ltd Thermal transfer sheet

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