JP2644999B2 - Thermal transfer ink - Google Patents

Thermal transfer ink

Info

Publication number
JP2644999B2
JP2644999B2 JP27630586A JP27630586A JP2644999B2 JP 2644999 B2 JP2644999 B2 JP 2644999B2 JP 27630586 A JP27630586 A JP 27630586A JP 27630586 A JP27630586 A JP 27630586A JP 2644999 B2 JP2644999 B2 JP 2644999B2
Authority
JP
Japan
Prior art keywords
wax
resin
viscosity
thermal transfer
ink
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP27630586A
Other languages
Japanese (ja)
Other versions
JPS63128992A (en
Inventor
信一郎 山口
幸一 坂井
浩 八嶋
雅則 湊
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP27630586A priority Critical patent/JP2644999B2/en
Priority to EP19870116658 priority patent/EP0268202B1/en
Priority to ES87116658T priority patent/ES2041254T3/en
Priority to DE87116658T priority patent/DE3786144T2/en
Priority to KR1019870012983A priority patent/KR920003247B1/en
Publication of JPS63128992A publication Critical patent/JPS63128992A/en
Application granted granted Critical
Publication of JP2644999B2 publication Critical patent/JP2644999B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • 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
    • B41M5/392Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents

Landscapes

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

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は安価で騒音が少なく取り扱いが容易であると
いう理由で使用分野が徐々に拡大してきている熱溶融転
写型プリンターに必要な熱転写用インクに関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a thermal transfer ink required for a hot-melt transfer printer whose field of use is gradually expanding because it is inexpensive, has low noise, and is easy to handle. About.

〔従来の技術及びその問題点〕[Conventional technology and its problems]

従来の熱転写用インクバインダーは、パラフィン、カ
ルナバといったワックスが主体で熱溶融時の粘度が極め
て低く、従って平滑性の良い熱転写専用紙に印字した場
合には、熱転写特有の光沢のある鮮明な印字を与えてい
た。しかし応用範囲が拡がるにつれて、より表面平滑性
の悪い紙への印字、印字堅牢性のある印字、高転写感度
印字、多数回使用印字といった様々な要求特性が発生し
てきた。このように要求特性が高度なものになるに従っ
て、従来のワックスだけで構成されるインクでは対応に
なかり無理がある事が判明し、樹脂を主体としたインク
の研究が各方面で進められている。
Conventional thermal transfer ink binders are mainly waxes such as paraffin and carnauba, and have extremely low viscosity when melted by heat.Therefore, when printing on thermal transfer paper with good smoothness, glossy clear print unique to thermal transfer is obtained. Was giving. However, as the range of application has been expanded, various required characteristics such as printing on paper having a poorer surface smoothness, printing with printing robustness, printing with high transfer sensitivity, and printing for multiple use have been generated. As the required properties become more advanced, it has been found that conventional inks consisting only of wax are too difficult to cope with, and research on resin-based inks has been advanced in various fields. I have.

高凝集力で造膜性があり粗表面紙への印字が期待され
る樹脂、高強度で堅牢印字が期待される樹脂、アモルフ
ァスで高転写感度印字が期待される樹脂、強い接着力が
あり多数回使用が期待される樹脂等があり、熱転写への
応用の可能性が昂まっている。しかし、一般に樹脂はワ
ックスに比べて溶融粘度が極めて高く、特にインク化し
た場合にはその傾向は顕著である。熱転写方式において
この溶融時の粘度は、被転写紙上への転写像形成を決め
る重要な因子であり、直接印字品質を左右する。熱溶融
状態においてワックスインクと同程度に低粘度であると
十分な接触面積が得られ、高被覆率の印字が達成できる
が、熱転写用に適した融点範囲を有する樹脂を主体とし
たインクでは一般的にワックス並の低粘度は熱転写時に
達成不可能である。
Resin expected to print on rough surface paper due to high cohesive strength, resin expected to print on rough surface paper, resin expected to print with high strength and robustness, resin expected to print with high transfer sensitivity amorphous, many with strong adhesive force There are resins and the like that are expected to be used once and the possibility of application to thermal transfer is increasing. However, resins generally have a much higher melt viscosity than waxes, and this tendency is particularly remarkable when made into ink. In the thermal transfer system, the viscosity at the time of melting is an important factor in determining the formation of a transferred image on a transfer paper, and directly affects the printing quality. In the hot melt state, if the viscosity is as low as that of the wax ink, a sufficient contact area can be obtained, and high coverage printing can be achieved. In general, a low viscosity comparable to that of wax cannot be achieved during thermal transfer.

この高粘度の樹脂インクを低粘度化して使いこなすた
めに従来は、オイル(ブチルセロソルブ,スピンドル油
等)の添加等で対応してきた。しかしオイルの添加は、
保存時のブリードアウトやブロッキングの問題があり、
十分な減粘効果を得るだけの量を添加する事が困難であ
った。
Conventionally, oil (such as butyl cellosolve, spindle oil, etc.) has been used to reduce the viscosity of the high-viscosity resin ink. But the addition of oil
If you have bleed-out or blocking issues on storage,
It was difficult to add an amount sufficient to obtain a sufficient viscosity reducing effect.

〔問題点を解決するための手段〕[Means for solving the problem]

本発明者らは上記の問題点を解決すべく鋭意研究の結
果、高溶融粘度のために従来使用不可能であった種々の
熱溶融性樹脂に、目的に応じて適当な減粘剤を添加して
粘度調整することにより、印字特性に優れた熱転写用イ
ンクが得られることを見出し本発明を完成するに至っ
た。
The present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, added an appropriate thickener according to the purpose to various heat-meltable resins which could not be used conventionally because of high melt viscosity. The present inventors have found that a thermal transfer ink having excellent printing characteristics can be obtained by adjusting the viscosity by the above method, and have completed the present invention.

即ち、本発明は、溶融粘度が1万〜100万cps(120℃
で測定)の樹脂をベースバインダーとして用いることに
より構成される溶液型の熱転写用インクであって、溶融
粘度の低減を目的として溶融粘度が1〜600cps(120℃
で測定)で、且つ使用する溶剤に一部可溶(40℃で100g
の溶剤に少なくても1g以上溶解)であるワックス、高級
脂肪酸から選択した少なくとも一種類の減粘剤をベース
樹脂100重量部に対し20〜120重量部含有し、且つ該減粘
剤の一部不溶部分をエマルジョン、スラリー、あるいは
微粉体といった微粒子状態で含有することを特徴とする
溶液型の熱転写用インクを提供するものである。
That is, the present invention provides a melt viscosity of 10,000 to 1,000,000 cps (120 ° C.
Is a solution-type thermal transfer ink constituted by using a resin of the formula (1) as a base binder, and having a melt viscosity of 1 to 600 cps (120 ° C.) for the purpose of reducing the melt viscosity.
) And partially soluble in the solvent used (100 g at 40 ° C)
At least 1 g of at least one type of thickener selected from higher fatty acids, based on 100 parts by weight of the base resin, and a part of the thickener. It is an object of the present invention to provide a solution type thermal transfer ink characterized in that the insoluble portion is contained in the form of fine particles such as emulsion, slurry, or fine powder.

本発明の熱転写用インクは、樹脂をベースにした溶融
粘度が比較的高い熱転写用インクを低粘度化して使いこ
なすために、ワックスからなる減粘剤を添加して得られ
るものであり、且つ溶液インクにワックスからなる減粘
剤の一部不溶部分をエマルジョン,スラリー、微粉体と
いった微粒子状態で添加することによって得られるもの
である。
The thermal transfer ink of the present invention is obtained by adding a viscosity reducing agent composed of a wax in order to reduce the viscosity of a resin-based thermal transfer ink having a relatively high melt viscosity and to use it. To a partially insoluble portion of a wax thinner in the form of fine particles such as emulsions, slurries, and fine powders.

本発明の熱転写用インクを既存のグラビア塗工機等に
よって基材上に塗布し乾燥する事により、高粘度の樹脂
とワックスからなる減粘剤の相溶性をまったく考慮する
事なく熱転写用インクシートを得ることができる。
By applying the thermal transfer ink of the present invention onto a substrate using an existing gravure coating machine or the like and drying it, the thermal transfer ink sheet can be used without any consideration of the compatibility of the thickener composed of a high-viscosity resin and wax. Can be obtained.

本発明により、いかなる高粘度のベース樹脂とワック
スからなる減粘剤との組み合わせも可能であり、あらゆ
る高粘度の樹脂を熱転写用のインクバインダーとして使
用する事が可能となった。
According to the present invention, any combination of a high-viscosity base resin and a wax-based thinning agent is possible, and any high-viscosity resin can be used as an ink binder for thermal transfer.

本発明に使用し得るベースバインダーとしての樹脂
は、溶融粘度が1万〜100万cps(120℃で測定)の樹脂
であり、例えば、ポリエステル樹脂,ポリアミド樹脂,
アクリル樹脂,ポリスチレン樹脂,ポリスチレンアクリ
ル樹脂,塩化ビニル樹脂,ポリビニルブチラール樹脂,
エポキシ樹脂,エチレン酢酸ビニル樹脂,ポリウレタン
樹脂,ポリカーボネート樹脂等、融点範囲60〜120℃の
樹脂及びそれらの混合物が挙げられる。
The resin as a base binder that can be used in the present invention is a resin having a melt viscosity of 10,000 to 1,000,000 cps (measured at 120 ° C.), for example, a polyester resin, a polyamide resin,
Acrylic resin, polystyrene resin, polystyrene acrylic resin, vinyl chloride resin, polyvinyl butyral resin,
Examples thereof include resins having a melting point in the range of 60 to 120 ° C., such as epoxy resins, ethylene vinyl acetate resins, polyurethane resins, and polycarbonate resins, and mixtures thereof.

本発明に使用できる低粘度減粘剤としては、120℃で
測定した溶融粘度が1〜600cpsで、且つ使用する溶媒に
一部可溶(40℃で100gの溶剤に少なくても1g以上溶解)
であるワックスから選択した少なくとも一種類のもので
あれば、すべてのものが使用可能である。しかしより好
ましくは120℃での溶融粘度が1〜400cpsであるワック
スが望ましい。
The low-viscosity reducing agent that can be used in the present invention has a melt viscosity measured at 120 ° C. of 1 to 600 cps, and is partially soluble in the solvent used (at least 1 g dissolved in 100 g solvent at 40 ° C.)
All of them can be used as long as they are at least one kind selected from waxes. However, a wax having a melt viscosity at 120 ° C. of 1 to 400 cps is more preferable.

本発明に使用し得るワックスとしては、カルナバワッ
クス,キャンデリラワックス,オリキュリーワックス,
サトウキビロウ,木ロウ等の天然植物ロウ,蜜ロウ,鯨
ロウ,中国ロウ,羊毛ロウ等の天然動物ロウ、パラフィ
ンワックス,マイクロクリスタリンワックス,酸化パラ
フィンワックス,酸化マイクロクリスタリンワックス等
の石油ワックス、モンタンワックス,オゾケライト,セ
レシン,リグナイトワックス等の鉱物系ワックスあるい
はケトンワックス,フィッシャー・トロプシュワック
ス,カスターワックス,オパールワックス,アーマーワ
ックス,アクラワックス等の合成ワックス及びそれらの
変成品といったあらゆるワックスが挙げられる。
Examples of the wax that can be used in the present invention include carnauba wax, candelilla wax, oricure wax,
Natural plant waxes such as sugarcane wax, wood wax, natural animal waxes such as beeswax, whale wax, Chinese wax, wool wax, petroleum waxes such as paraffin wax, microcrystalline wax, oxidized paraffin wax, oxidized microcrystalline wax, and montan wax And mineral waxes such as ozokerite, ceresin, lignite wax, and synthetic waxes such as ketone wax, Fischer-Tropsch wax, caster wax, opal wax, armor wax, and accra wax, and modified waxes thereof.

本発明に使用できる溶剤は、エタノール,イソプロピ
ルアルコール等のアルコール類、メチルエチルケトン,
メチルイソブチルケトン等のケトン類、トルエン,キシ
レン等の芳香族系の溶剤、及び水等、通常インク、塗料
に使用されている溶剤であればあらゆる溶剤が使用可能
である。また必要に応じてこれらの溶剤を混合して用い
ても良い。
Solvents usable in the present invention include alcohols such as ethanol and isopropyl alcohol, methyl ethyl ketone,
Any solvent can be used as long as it is a solvent generally used in inks and coatings, such as ketones such as methyl isobutyl ketone, aromatic solvents such as toluene and xylene, and water. If necessary, these solvents may be mixed and used.

本発明の熱転写用インクを用いて熱転写用インクシー
トを製造するには、基材上又は基材上の塗膜層と接触し
て本発明の熱転写用インクを少なくとも一層塗布し、乾
燥すれば良く、その他上塗層又は通電発熱用抵抗層・導
電層等他の構成層と共に使用することもできる。
To produce a thermal transfer ink sheet using the thermal transfer ink of the present invention, at least one layer of the thermal transfer ink of the present invention is applied in contact with the substrate or a coating layer on the substrate, and may be dried. It can also be used together with other constituent layers such as an overcoat layer or a resistive layer for conducting and heating and a conductive layer.

本発明の熱転写用インクは通常塗工機或いは印刷機に
よって基材上に塗布する。その際、添加する減粘剤が使
用溶剤に全く不溶であると、析出粒子間の相互作用が強
くなり、構造粘性が増大し、塗工・印刷時のグラビア目
からの離脱及び塗布直後のレベリングが問題となり、き
れいな塗布面が得られ難い。しかし本発明では、添加す
る減粘剤が使用溶剤に一部可溶であるため、構造粘性を
抑制する事ができ、その結果良好な塗工性、印刷適性が
達成される。
The ink for thermal transfer of the present invention is usually applied onto a substrate by a coating machine or a printing machine. At that time, if the added viscosity reducing agent is completely insoluble in the solvent used, the interaction between the precipitated particles becomes stronger, the structural viscosity increases, the coating is released from the gravure at the time of coating and printing, and the leveling is performed immediately after coating. Is a problem, and it is difficult to obtain a clean coating surface. However, in the present invention, since the added viscosity reducing agent is partially soluble in the solvent used, the structural viscosity can be suppressed, and as a result, good coating properties and printability can be achieved.

〔実施例〕〔Example〕

以下実施例により本発明の有効性を例示するが、もと
より本発明はこれらに限定されるものではない。
Hereinafter, the effectiveness of the present invention will be illustrated by examples, but the present invention is not limited to these examples.

実施例1 軟化点90℃のポリエステル樹脂(120℃での溶融粘度2
3000cps)を主体とした下記の組成比からなる溶剤系の
熱転写用インクを調整した。
Example 1 Polyester resin having a softening point of 90 ° C. (melt viscosity at 120 ° C. 2
A solvent-based thermal transfer ink composed mainly of 3000 cps) and having the following composition ratio was prepared.

これとは別にトルエンを用いたカルナバワックススラ
リーの溶液を準備した。これは熱トルエン中でカルナ
バワックスを完全溶解させ、その後冷却して製造したス
ラリーでも良いし、トルエンにカルナバワックス微粉を
添加後必要に応じて分散させたスラリーでも性能的には
良い。
Separately, a carnauba wax slurry solution using toluene was prepared. This may be a slurry prepared by completely dissolving carnauba wax in hot toluene and then cooling it, or a slurry prepared by adding carnauba wax fine powder to toluene and then dispersing as necessary.

更にインクにスラリーを添加してインク〜イン
クを調整した。
Further, a slurry was added to the ink to prepare ink to ink.

これらのインクを3.5μのポリエチレンテレフタレー
ト(PET)フィルム上に塗布後乾燥して熱転写用インク
シートを作成した。
These inks were applied on a 3.5 μm polyethylene terephthalate (PET) film and dried to prepare a thermal transfer ink sheet.

得られた熱転写用インクシートについて市販の熱転写
用プリンターで印字評価を行った。評価結果は表1にま
とめて記載してあるが、カルナバワックススラリーの添
加量の増加と共に減粘効果が起こり堅牢性等、樹脂の特
徴を維持したままでワックスインクと同程度の転写率・
解像度を持った熱転写像が得られることが判る。
Printing evaluation was performed on the obtained thermal transfer ink sheet using a commercially available thermal transfer printer. The evaluation results are summarized in Table 1. As the addition amount of the carnauba wax slurry increases, the viscosity reduction effect occurs, and the transfer rate and the transfer rate are almost the same as those of the wax ink while maintaining the characteristics of the resin such as the robustness.
It can be seen that a thermal transfer image having a resolution can be obtained.

比較例1 実施例1におけるインクを用いて実施例1と同条件
で熱転写像を得た。
Comparative Example 1 A thermal transfer image was obtained using the ink of Example 1 under the same conditions as in Example 1.

印字詳細結果を表1に示す。この場合は、極めて高粘
度なインクとなるため充分な転写が得られず被覆率の低
い転写像となった。
Table 1 shows the detailed printing results. In this case, since the ink had an extremely high viscosity, sufficient transfer was not obtained, and a transferred image having a low coverage was obtained.

実施例2 軟化点86℃のポリアミド樹脂(120℃での溶融粘度175
00)、軟化点102℃のポリスチレンアクリル樹脂(120℃
での溶融粘度50000)、又は軟化点78℃のポリスチレン
樹脂(120℃での溶融粘度11000)を主成分として構成し
た溶剤系インク(溶剤はいずれもトルエン/メチルエチ
ルケトン=1/1)に、実施例1と同様の方法で準備した
ポリエチレンワックス(120℃での溶融粘度30cps)とカ
ルナバワックスの1対1混合スラリーを対樹脂比で10,2
0,30,40,50%,150%添加してインクを調整した。
Example 2 Polyamide resin having a softening point of 86 ° C (melt viscosity at 120 ° C of 175)
00), polystyrene acrylic resin with a softening point of 102 ° C (120 ° C
Example 1 was prepared using a solvent-based ink composed mainly of a polystyrene resin having a softening point of 78 ° C. (melt viscosity of 50,000 at 120 ° C.) or a polystyrene resin having a softening point of 78 ° C. (solvent: toluene / methyl ethyl ketone = 1/1). A 1: 1 mixed slurry of polyethylene wax (melt viscosity at 120 ° C. 30 cps) and carnauba wax prepared in the same manner as in Example 1 in a resin-to-resin ratio of 10,2
The inks were adjusted by adding 0, 30, 40, 50% and 150%.

実施例1と同様の印字評価を行った所、表2に示す様
な結果が得られ明らかに減粘効果があることが認められ
た。
When the same printing evaluation as in Example 1 was performed, the results shown in Table 2 were obtained, and it was confirmed that there was a clear viscosity reducing effect.

実施例3 融点105℃のパラフィンワックス(120℃での溶融粘度
23cps)を用いてトルエン中でスラリーを作り、実施例
1に記載したポリエステル樹脂に対樹脂重量比30%添加
してインクを作成した。実施例1と同様の印字評価を行
った所、表3に示すような結果が得られた。
Example 3 Paraffin wax having a melting point of 105 ° C. (melt viscosity at 120 ° C.)
A slurry was prepared in toluene using 23 cps) and added to the polyester resin described in Example 1 at a resin weight ratio of 30% to prepare an ink. When the same printing evaluation as in Example 1 was performed, the results shown in Table 3 were obtained.

表3から明らかなように、十分な減粘効果が現れ良好
な印字特性を持ったインクが調整された。このように融
点100℃を越える高融点ワックスでも溶融粘度が低けれ
ば減粘作用を発揮することが判った。
As is clear from Table 3, an ink having a sufficient viscosity reducing effect and having good printing characteristics was prepared. As described above, it was found that even a high melting point wax having a melting point exceeding 100 ° C. exhibited a viscosity reducing effect if the melt viscosity was low.

実施例4 軟化点106℃のポリアミド樹脂(120℃での溶融粘度12
0000cps)を通常の方法でエマルジョン化して、エマル
ジョンインクを作成した。これとは別に一般に用いられ
る乳化剤により融点87℃の変成マイクロクリスタリンワ
ックス(120℃での溶融粘度4cps)を乳化し同様のエマ
ルジョンを準備し、上記エマルジョンインクに対樹脂重
量比20%添加してインクを作成した。実施例1と同様の
印字評価を行った所、表3に示すような結果が得られ
た。
Example 4 Polyamide resin having a softening point of 106 ° C. (melt viscosity at 120 ° C. 12
0000 cps) was emulsified in a usual manner to prepare an emulsion ink. Separately, denatured microcrystalline wax having a melting point of 87 ° C. (melt viscosity at 120 ° C. 4 cps) is emulsified with a commonly used emulsifier to prepare a similar emulsion. It was created. When the same printing evaluation as in Example 1 was performed, the results shown in Table 3 were obtained.

表3より明らかなように印字特性の良好なエマルジョ
ンインクが調整された。
As is clear from Table 3, an emulsion ink having good printing characteristics was prepared.

比較例2 実施例1で用いた樹脂インクに融点78℃のポリエステ
ル樹脂(120℃での溶融粘度2300cps)を対樹脂比30%添
加してインクを作成した。実施例1と同様の印字評価を
行った所、表3に示すような結果が得られた。
Comparative Example 2 An ink was prepared by adding a polyester resin having a melting point of 78 ° C. (melt viscosity at 120 ° C., 2300 cps) to the resin ink used in Example 1 at a ratio of 30% to the resin. When the same printing evaluation as in Example 1 was performed, the results shown in Table 3 were obtained.

表3から明らかな如く、若干の粘度低下は認められた
ものの良好な印字特性を与える程には減粘効果を示さな
かった。このように低融点樹脂でも本発明の範囲以外の
溶融粘度を有するものは、著しく効果が低いことが証明
された。
As is evident from Table 3, although a slight decrease in viscosity was observed, no viscosity-reducing effect was exhibited to give good printing characteristics. As described above, it has been proved that even a low melting point resin having a melt viscosity outside the range of the present invention has a remarkably low effect.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭61−37472(JP,A) 特開 昭61−51386(JP,A) 特開 昭63−89386(JP,A) 特開 昭61−68290(JP,A) 特開 昭60−166485(JP,A) ──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-61-37472 (JP, A) JP-A-61-51386 (JP, A) JP-A-63-89386 (JP, A) JP-A-61-37386 68290 (JP, A) JP-A-60-166485 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】溶融粘度が1万〜100万cps(120℃で測
定)の樹脂をベースバインダーとして用いることにより
構成される溶液型の熱転写用インクであって、溶融粘度
の低減を目的として溶融粘度が1〜600cps(120℃で測
定)で、且つ使用する溶剤に一部可溶(40℃で100gの溶
剤に少なくても1g以上溶解)であるワックスから選択し
た少なくとも一種類の減粘剤をベース樹脂100重量部に
対し20〜120重量部含有し、且つ、該減粘剤の一部不溶
部分をエマルジョン、スラリー、あるいは微粉体といっ
た微粒子状態で含有することを特徴とする溶液型の熱転
写用インク。
1. A solution type thermal transfer ink comprising a resin having a melt viscosity of 10,000 to 1,000,000 cps (measured at 120 ° C.) as a base binder. At least one kind of viscosity reducing agent selected from waxes having a viscosity of 1 to 600 cps (measured at 120 ° C) and being partially soluble in the solvent used (at least 1 g soluble in 100 g solvent at 40 ° C) 20 to 120 parts by weight with respect to 100 parts by weight of the base resin, and a partially insoluble portion of the thickener is contained in the form of fine particles such as an emulsion, a slurry, or a fine powder. For ink.
JP27630586A 1986-11-19 1986-11-19 Thermal transfer ink Expired - Fee Related JP2644999B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP27630586A JP2644999B2 (en) 1986-11-19 1986-11-19 Thermal transfer ink
EP19870116658 EP0268202B1 (en) 1986-11-19 1987-11-11 Thermal transfer ink
ES87116658T ES2041254T3 (en) 1986-11-19 1987-11-11 INK FOR THERMAL TRANSFER.
DE87116658T DE3786144T2 (en) 1986-11-19 1987-11-11 Thermal transfer ink.
KR1019870012983A KR920003247B1 (en) 1986-11-19 1987-11-18 Thermal transfer ink

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27630586A JP2644999B2 (en) 1986-11-19 1986-11-19 Thermal transfer ink

Publications (2)

Publication Number Publication Date
JPS63128992A JPS63128992A (en) 1988-06-01
JP2644999B2 true JP2644999B2 (en) 1997-08-25

Family

ID=17567599

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27630586A Expired - Fee Related JP2644999B2 (en) 1986-11-19 1986-11-19 Thermal transfer ink

Country Status (5)

Country Link
EP (1) EP0268202B1 (en)
JP (1) JP2644999B2 (en)
KR (1) KR920003247B1 (en)
DE (1) DE3786144T2 (en)
ES (1) ES2041254T3 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2823124B2 (en) 1988-05-19 1998-11-11 フジコピアン株式会社 Thermal transfer ink

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2567039B2 (en) * 1988-06-17 1996-12-25 キヤノン株式会社 Double recording method
JPH0238470A (en) * 1988-07-29 1990-02-07 Dainippon Printing Co Ltd Ink composition and its production
JPH0248628A (en) * 1988-08-11 1990-02-19 Toshiba Corp Endoscopic device
US5401606A (en) * 1993-04-30 1995-03-28 E. I. Du Pont De Nemours And Company Laser-induced melt transfer process
US5757313A (en) * 1993-11-09 1998-05-26 Markem Corporation Lacer-induced transfer printing medium and method
US5739189A (en) * 1995-12-18 1998-04-14 Ncr Corporation Low energy thermal transfer formulation
GB2324163B (en) * 1997-04-11 2002-03-20 Ncr Int Inc Thermal transfer medium

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3315249C2 (en) * 1983-04-27 1987-01-22 Renker GmbH & Co KG, 5160 Düren Heat-sensitive recording/transfer material and process for its manufacture
JPS60115487A (en) * 1983-11-29 1985-06-21 Konishiroku Photo Ind Co Ltd Thermal transfer recording medium
JPS60178091A (en) * 1984-02-24 1985-09-12 Fujitsu Ltd Ink sheet for heat transfer recording
JPS60183195A (en) * 1984-02-29 1985-09-18 Fujitsu Ltd Thermal transfer recording sheet

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2823124B2 (en) 1988-05-19 1998-11-11 フジコピアン株式会社 Thermal transfer ink

Also Published As

Publication number Publication date
JPS63128992A (en) 1988-06-01
ES2041254T3 (en) 1993-11-16
EP0268202A3 (en) 1989-11-29
DE3786144T2 (en) 1993-12-02
KR920003247B1 (en) 1992-04-25
EP0268202A2 (en) 1988-05-25
KR880006333A (en) 1988-07-22
EP0268202B1 (en) 1993-06-09
DE3786144D1 (en) 1993-07-15

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