JPH03266692A - Sublimation type thermal transfer material - Google Patents
Sublimation type thermal transfer materialInfo
- Publication number
- JPH03266692A JPH03266692A JP2064065A JP6406590A JPH03266692A JP H03266692 A JPH03266692 A JP H03266692A JP 2064065 A JP2064065 A JP 2064065A JP 6406590 A JP6406590 A JP 6406590A JP H03266692 A JPH03266692 A JP H03266692A
- Authority
- JP
- Japan
- Prior art keywords
- ink layer
- polydimethylsiloxane
- binder
- thermal transfer
- transfer material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000859 sublimation Methods 0.000 title claims abstract description 17
- 230000008022 sublimation Effects 0.000 title claims abstract description 17
- 239000000463 material Substances 0.000 title claims abstract description 16
- -1 polydimethylsiloxane Polymers 0.000 claims abstract description 24
- 239000004205 dimethyl polysiloxane Substances 0.000 claims abstract description 21
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 21
- 239000011230 binding agent Substances 0.000 claims abstract description 16
- 125000000524 functional group Chemical group 0.000 claims abstract description 15
- 239000000758 substrate Substances 0.000 claims abstract description 6
- 238000011109 contamination Methods 0.000 abstract description 4
- 230000000740 bleeding effect Effects 0.000 abstract description 2
- 238000002425 crystallisation Methods 0.000 abstract description 2
- 230000008025 crystallization Effects 0.000 abstract description 2
- 238000002844 melting Methods 0.000 abstract description 2
- 230000008018 melting Effects 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 44
- 239000000975 dye Substances 0.000 description 16
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000007788 liquid Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 229920001296 polysiloxane Polymers 0.000 description 7
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 4
- 230000004927 fusion Effects 0.000 description 3
- 125000005395 methacrylic acid group Chemical group 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 229920003235 aromatic polyamide Polymers 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- VGKYEIFFSOPYEW-UHFFFAOYSA-N 2-methyl-4-[(4-phenyldiazenylphenyl)diazenyl]phenol Chemical compound Cc1cc(ccc1O)N=Nc1ccc(cc1)N=Nc1ccccc1 VGKYEIFFSOPYEW-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- FHNINJWBTRXEBC-UHFFFAOYSA-N Sudan III Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC(C=C1)=CC=C1N=NC1=CC=CC=C1 FHNINJWBTRXEBC-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- PXOZAFXVEWKXED-UHFFFAOYSA-N chembl1590721 Chemical compound C1=CC(NC(=O)C)=CC=C1N=NC1=CC(C)=CC=C1O PXOZAFXVEWKXED-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、昇華型熱転写体に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to a sublimation type thermal transfer material.
[従来の技術]
従来、基体上に樹脂結着剤中に昇華性染料を分散したイ
ンク層を設けてなる昇華型熱転写体のインク層面に受像
シートを重ねて、転写体側からレーザーやサーマルヘッ
ド等の電気信号により制御された熱エネルギーを印加し
て、その部分のインクを受像シート上に昇華移行させる
ことにより画像を形成する方式がある。[Prior art] Conventionally, an image-receiving sheet is placed on the ink layer surface of a sublimation type thermal transfer body, which has an ink layer in which a sublimable dye is dispersed in a resin binder on a substrate, and a laser or a thermal head, etc. is applied from the transfer body side. There is a method of forming an image by applying thermal energy controlled by an electric signal to sublimate and transfer the ink in that area onto the image receiving sheet.
二の昇華転写方式は原理的にサーマルヘッド等からの熱
エネルギーに対応して染料が単分子状で昇華するため、
容易に中間調が得られ、かつ随意に階調をコントロール
することか可能である利点を有し、フルカラープリンタ
ーに最も適した方式と考えられている。In principle, the second sublimation transfer method sublimates the dye in monomolecular form in response to thermal energy from a thermal head, etc.
This method has the advantage of easily obtaining halftones and allowing the gradation to be controlled at will, and is considered the most suitable method for full-color printers.
[発明が解決しようとする課題]
ところで、昇華型熱転写方式にはワンタイム記録法とマ
ルチ記録法があるが、前者では受像層の筆記性、画像安
定性を向上するため、又、後者ではインク層と受像層と
の間の摩擦力、加熱軟化による融着等を防止するため、
転写体のインク層中に滑性又は離型性を有する物質を混
合することを提案した。[Problems to be Solved by the Invention] By the way, there are two types of sublimation thermal transfer methods: a one-time recording method and a multi-recording method. In order to prevent frictional force between the layer and the image-receiving layer, fusion due to heat softening, etc.
It was proposed that a substance having lubricity or release properties be mixed into the ink layer of the transfer body.
インク層中に滑性又は離型性物質を添加することにより
一定の改善は達成させるものの、−方インク層中に添加
される上記物質は一般にインク層中の結着剤と非相溶性
であり、保存中にインク層表面にブリードしやすい。Although certain improvements can be achieved by adding lubricating or releasing substances to the ink layer, the above substances added to the ink layer are generally incompatible with the binder in the ink layer. , easy to bleed onto the surface of the ink layer during storage.
又、ガラス転移温度、溶融温度、軟化温度が低いため、
含有量が増加する共にインク層の保存性が低下し、結果
的にインク層保存時に未使用染料が結晶化したり、イン
ク層表面に析出したりし、又、記録時には非画像部にも
地肌汚れが生じたり、耐熱層汚染からサーマルヘッドを
汚染したりする等という問題も発生する。In addition, because the glass transition temperature, melting temperature, and softening temperature are low,
As the content increases, the storage stability of the ink layer decreases, resulting in unused dye crystallizing or depositing on the surface of the ink layer during storage, and also causing background stains in non-image areas during recording. Problems also occur, such as the thermal head being contaminated due to contamination of the heat-resistant layer.
本発明は、こうした実状に鑑み、受像シートとの間の滑
性、離型性に優れると共に、保存性においても優れた昇
華型熱転写体を提供することを目的とするものである。In view of these circumstances, it is an object of the present invention to provide a sublimation type thermal transfer material that is excellent in lubricity between the material and the image-receiving sheet and mold releasability, and also has excellent preservability.
5課題を解決するための手段]
本発明者らは、前記した課題を解決するため鋭意検討し
てきた結果、インク層中に結着剤と反応性の官能基を分
子片末端のみに有するポリジメチルシロキサンを添加す
ることが有効であることを知見し、本発明に至った。Means for Solving 5 Problems] As a result of intensive studies to solve the above-mentioned problems, the present inventors have discovered that polydimethyl has a functional group reactive with a binder only at one end of the molecule in the ink layer. It was discovered that adding siloxane was effective, leading to the present invention.
すなわち、本発明は、基体上に昇華性染料を結着剤中に
分散したインク層を有する昇華型熱転写体において、前
記インク層中に結着剤と反応する官能基を分子の片方の
末端のみに有するポリジメチルシロキサンを含有する昇
華型熱転写体である。That is, the present invention provides a sublimation thermal transfer material having an ink layer on a substrate in which a sublimable dye is dispersed in a binder, in which a functional group that reacts with the binder is contained in the ink layer only at one end of the molecule. This is a sublimation type thermal transfer material containing polydimethylsiloxane.
本発明の昇華型熱転写体は、上記のようにインク層中の
ポリジメチルシロキサンの一方の分子末端のみが結着剤
と反応し、他端はフリーであるため、ポリジメチルシロ
キサンはインク層表面にブリードすることなく、又、ポ
リジメチルシロキサンがインク層表面側に配向する。そ
のためインク層中の結着剤中に分散されている染料が表
面に析出し、受像層の地肌汚れや染料の結晶化、耐熱層
、サーマルヘッド汚染等が発生しにくくなる。In the sublimation thermal transfer material of the present invention, as described above, only one molecular end of the polydimethylsiloxane in the ink layer reacts with the binder, and the other end is free. Polydimethylsiloxane is oriented toward the surface of the ink layer without bleeding. Therefore, the dye dispersed in the binder in the ink layer precipitates on the surface, making it difficult to cause background stains on the image-receiving layer, crystallization of the dye, contamination of the heat-resistant layer, and the thermal head.
又、インク層表面側に配向したポリジメチルシロキサン
自体は滑性、離型性能を有するので、インク層の融着防
止能力は保持されており記録時の不都合は生じない。Furthermore, since the polydimethylsiloxane oriented on the surface side of the ink layer itself has lubricity and release properties, the ability to prevent the ink layer from adhesion is maintained, and no inconvenience occurs during recording.
すなわち、本発明の昇華型熱転写体は、滑性、離型性良
好でかつインク層の保存性も良好である。That is, the sublimation type thermal transfer material of the present invention has good lubricity and release properties, and also has good storage stability of the ink layer.
本発明の昇華型熱転写体に使用される昇華染料、結着剤
等は公知のものが使用できる。Known sublimation dyes, binders, etc. can be used in the sublimation type thermal transfer material of the present invention.
昇華性染料としては60℃以上で昇華あるいは気化する
染料であり、主に分散染料、油溶性染料などの熱転写記
録の分野で使用されるものであればよく、例えばC31
,デイスパースイエローの1.3.8,9.1B、41
.54.[io、77、lieなど、C11,デイスパ
ースレッドの1.4.6.11.15,17.55.5
9.60.7383など、C,1,デイスパースブルー
の3.14,19.28゜5B、60,64,72,9
9,108など、C,1,ソルベントイエローの77.
116など、C,1,ソルベントレッドの23゜25.
27など、C11,ソルベントブルーのae、ga。Sublimable dyes are dyes that sublimate or vaporize at temperatures above 60°C, and are mainly used in the field of thermal transfer recording such as disperse dyes and oil-soluble dyes, such as C31.
, Disperse Yellow 1.3.8, 9.1B, 41
.. 54. [io, 77, lie, etc., C11, dispers thread 1.4.6.11.15, 17.55.5
9.60.7383 etc., C, 1, Disperse Blue 3.14, 19.28° 5B, 60, 64, 72, 9
9,108 etc., C, 1, Solvent Yellow 77.
116 etc., C, 1, Solvent Red 23°25.
27 etc., C11, solvent blue ae, ga.
105などが挙げられる。これらの染料は単独又は数種
混合して使用される。105 and the like. These dyes may be used alone or in combination.
インク層に使用される結着剤には熱可塑性または熱硬化
性樹脂が用いられ、そのうち比較的高ガラス転移点又は
高軟化性を有する樹脂としては、例えば塩化ビニル樹脂
、酢酸ビニル樹脂、ポリアミド、ポリエチレン、ポリカ
ーボネート、ポリスチレン、ポリプロピレン、アクリル
樹脂、フェノール樹脂、ポリエステル、ポリウレタン、
エポキシ樹脂、シリコーン樹脂、フッ素樹脂、ブチラー
ル樹脂、メラミン樹脂、天然ゴム、合成ゴム、ポリビニ
ルアルコール、セルロース樹脂が挙げられるが、これら
の樹脂の一部又は全部はポリジメチルシロキサン分子の
片末端に存在する官能基と反応する官能基を有している
ものである。Thermoplastic or thermosetting resins are used as binders for the ink layer, and examples of resins with relatively high glass transition points or high softening properties include vinyl chloride resins, vinyl acetate resins, polyamides, Polyethylene, polycarbonate, polystyrene, polypropylene, acrylic resin, phenolic resin, polyester, polyurethane,
Examples include epoxy resin, silicone resin, fluororesin, butyral resin, melamine resin, natural rubber, synthetic rubber, polyvinyl alcohol, and cellulose resin, but some or all of these resins exist at one end of the polydimethylsiloxane molecule. It has a functional group that reacts with a functional group.
又、インク層中に含有する分子の片方の末端のみに官能
基を有するポリジメチルシロキサンにおいて、反応性官
能基として、アミノ、エポキシ、エポキシ−ポリエーテ
ル、カルボキシルメルカプト、ヒドロキシル等がある。In polydimethylsiloxane containing a functional group at only one end of the molecule contained in the ink layer, the reactive functional group includes amino, epoxy, epoxy-polyether, carboxylmercapto, hydroxyl, and the like.
この物質のインク層中の含有量は5〜50重量%が好ま
しい。The content of this substance in the ink layer is preferably 5 to 50% by weight.
前記含有量が5%未満では離型性、滑性効果が不充分で
あり、一方、5%を越えると保存性において問題を生ず
る。If the content is less than 5%, the mold releasability and lubricity effects will be insufficient, while if it exceeds 5%, problems will occur in storage stability.
又、インク層の染料濃度は通常5〜80%、好ましくは
10〜60%程度である。Further, the dye concentration of the ink layer is usually about 5 to 80%, preferably about 10 to 60%.
又、基体シートとしてはコンデンサーベーバポリエステ
ルフィルム、ポリスチレンフィルム、ポリサルホンフィ
ルム、ポリイミドフィルム、ポリアミドフィルム等のフ
ィルムが使用され基体シートとインク層との間には必要
に応じて従来慣用の接着層などを設けてもよく、又、基
体シートの裏面には必要に応じて従来慣用の耐熱性潤滑
層を設けてもよい。Further, as the base sheet, a film such as a capacitor Baba polyester film, a polystyrene film, a polysulfone film, a polyimide film, a polyamide film, etc. is used, and a conventional adhesive layer or the like is used between the base sheet and the ink layer as necessary. Alternatively, a conventional heat-resistant lubricant layer may be provided on the back surface of the base sheet, if necessary.
[実施例]
以下、本発明を下記の実施例に基づいて更に具体的に説
明するか、本発明はこれらに限定されるものではない。[Examples] Hereinafter, the present invention will be explained in more detail based on the following examples, but the present invention is not limited thereto.
実施例1
ポリビニルブチラールBX−1[積水
化学工業■] 7重量部昇華性染
料Kayaset Blue 7J4[日本化薬■]
7重量部エポキシ官能基を片方に有
するポ
リジメチルシロキサンBX1B−191[トーμ・シリ
コーン■] 3重量部ジイソシアネート・
コロネートし2重量部トルエン
70重量部メチルエチルケトン 70重量部
上記処方の組成物を24時間ボールミルにて分散後、裏
面に1μ閣厚のシリコーン樹脂系耐熱層を形成した6μ
層厚のポリエチレンテレフタレートフィルムにワイヤー
バーを用いて1.0μI厚のシアンインク層を形成した
。これを更に60℃24時間保存し、転写体を得た。Example 1 Polyvinyl butyral BX-1 [Sekisui Chemical ■] 7 parts by weight sublimable dye Kayaset Blue 7J4 [Nippon Kayaku ■]
7 parts by weight Polydimethylsiloxane BX1B-191 having an epoxy functional group on one side [Toμ・Silicone■] 3 parts by weight Diisocyanate・
Coronate and 2 parts by weight toluene
70 parts by weight Methyl ethyl ketone 70 parts by weight After dispersing the composition of the above formulation in a ball mill for 24 hours, a 6μ thick silicone resin heat-resistant layer with a thickness of 1 μm was formed on the back side.
A cyan ink layer having a thickness of 1.0 μI was formed on a polyethylene terephthalate film using a wire bar. This was further stored at 60°C for 24 hours to obtain a transcript.
比較例1
実施例1においてエポキシ官能基を片方に有するポリジ
メチルシロキサンをジメチルポリシロキサンSH200
オイル(トーμシリコーン■)に変えた以外は実施例1
と同様にして転写体を得た。Comparative Example 1 In Example 1, polydimethylsiloxane having an epoxy functional group on one side was replaced with dimethylpolysiloxane SH200.
Example 1 except that oil (to μ silicone ■) was used.
A transfer material was obtained in the same manner as described above.
実施例2
実施例1において昇華性染料Kayaset Blue
7147重量部を14重量部とし、基体を芳香族ポリア
ミドフィルムとし、インク層厚を 3.0μ腸とした他
は全て実施例1と同様にして転写体を得た。Example 2 In Example 1, the sublimable dye Kayaset Blue
A transfer body was obtained in the same manner as in Example 1, except that 7147 parts by weight was changed to 14 parts by weight, the substrate was an aromatic polyamide film, and the ink layer thickness was changed to 3.0 μm.
比較例2
実施例2においてエポキシ官能基を片方に有するポリジ
メチルシロキサンをジメチルポリシロキサンS)I 2
00オイルに変えた他は全て実施例2と同様にして熱転
写体を得た。Comparative Example 2 In Example 2, the polydimethylsiloxane having an epoxy functional group on one side was replaced with dimethylpolysiloxane S)I 2
A thermal transfer body was obtained in the same manner as in Example 2 except that 00 oil was used.
実施例3
ウレタンアクリレートV−4801(大日本インキ化学
工業■) 9重量部ビニルピロリドン
1重量部イルガキュア#651 (チバガ
イギ)0.3重量部
昇華性染料Kayaset Blue 714 10
重量部メタクリル官能基を片方に有する
ポリジメチルシロキサンBX1B−1925重量部
トルエン 100重量部酢酸ブチ
ル 80重量部イソブタノール
20重量部上記処方の組成物を24時間ボ
ールミルにて分散後、裏面に 1μI厚のシリコーン樹
脂系耐熱層を形成した6μI厚のポリエチレンテレフタ
レートフィルムにワイヤーバーを用いて1.0μI厚の
インク層を形成した。これを高圧水銀灯(80W/cm
)で照射時間10秒にて紫外線硬化させ転写体を得た。Example 3 Urethane acrylate V-4801 (Dainippon Ink & Chemicals ■) 9 parts by weight vinylpyrrolidone
1 part by weight Irgacure #651 (Ciba Geigi) 0.3 parts by weight Sublimation dye Kayaset Blue 714 10
Parts by weight Polydimethylsiloxane with methacrylic functional group on one side BX1B-1925 parts by weight Toluene 100 parts by weight Butyl acetate 80 parts by weight Isobutanol
After dispersing 20 parts by weight of the above composition in a ball mill for 24 hours, a 1.0 μl thick ink layer was applied to a 6 μl thick polyethylene terephthalate film with a 1 μl thick silicone resin heat-resistant layer formed on the back side using a wire bar. Formed. This is a high pressure mercury lamp (80W/cm
) for an irradiation time of 10 seconds to obtain a transfer body.
比較例3
実施例3においてメタクリル官能基を片方に有するポリ
ジメチルシロキサンをジメチルポリシロキサンSH20
0オイル(トーμ・シリコーン#)に変えた他は全て実
施例3と同様にして転写体を得た。Comparative Example 3 In Example 3, polydimethylsiloxane having a methacrylic functional group on one side was replaced with dimethylpolysiloxane SH20.
A transfer body was obtained in the same manner as in Example 3 except that the transfer material was changed to 0 oil (to μ silicone #).
実施例4
実施例3において昇華性染料Kayaset Blue
7147重量部を14重量部とし、基体を芳香族ポリア
ミドフィルムとし、インク層厚を 3.0μlとした他
は全て実施例3と同様にして転写体を得た。Example 4 In Example 3, the sublimable dye Kayaset Blue
A transfer body was obtained in the same manner as in Example 3 except that 7147 parts by weight was changed to 14 parts by weight, the substrate was an aromatic polyamide film, and the ink layer thickness was changed to 3.0 μl.
比較例4
実施例4においてメタクリル官能基を片方に有するポリ
ジメチルシロキサンをジメチルボリシロキサンSH20
0オイルに変えた他は全て実施例4と同様にして転写体
を得た。Comparative Example 4 In Example 4, polydimethylsiloxane having a methacrylic functional group on one side was replaced with dimethylborisiloxane SH20.
A transfer body was obtained in the same manner as in Example 4 except that the transfer material was changed to 0 oil.
又、下記組成の混合物を充分混合分散させ、染料受容層
用塗液[A液]を調製した。Further, a coating liquid for a dye-receiving layer [Liquid A] was prepared by thoroughly mixing and dispersing a mixture having the following composition.
[A液]
塩化ビニル/酢酸ビニル/ビニル
アルコール共重合体(商品名VAG)l ;ユニオンカ
ーバイド社製)10部
インシアネート(商品名コロネー
トム;日本ポリウレタン工業社製) 5部アミノ変性
シリコーン(商品名SF
−8417;東しシリコーン社製)0.5部エポキシ変
性シリコーン(商品名
SF−8411;東しシリコーン社製)0.4部トルエ
ン 40部メチルエチルケ
トン 40部次に[A液]をワイヤーバー
を用いて、厚さ約150μ腸の合成紙(商品名ユボFP
G−150、玉子油化合成紙社製)上に塗布し、乾燥温
度75℃で1分間乾燥して、厚さ約5μmの染料受容層
を形成させた後、更に80℃で3時間保存して硬化させ
、本発明の実施例2.4、比較例2.4用の受像媒体を
作成した。[Liquid A] Vinyl chloride/vinyl acetate/vinyl alcohol copolymer (trade name: VAG); manufactured by Union Carbide Co., Ltd.) 10 parts Incyanate (trade name: Coronatom; manufactured by Nippon Polyurethane Industries, Ltd.) 5 parts Amino-modified silicone (trade name) SF-8417; manufactured by Toshi Silicone Co., Ltd.) 0.5 parts Epoxy-modified silicone (trade name SF-8411; manufactured by Toshi Silicone Co., Ltd.) 0.4 parts Toluene 40 parts Methyl ethyl ketone 40 parts Next, [Liquid A] was mixed with a wire bar. Synthetic paper (trade name: Yubo FP) with a thickness of approximately 150μ
G-150, manufactured by Tamago Yuka Synthetic Paper Co., Ltd.) and dried for 1 minute at a drying temperature of 75°C to form a dye-receiving layer with a thickness of about 5 μm, and then stored at 80°C for 3 hours. This was cured to produce image receiving media for Example 2.4 of the present invention and Comparative Example 2.4.
[B液〕
ポリエステル樹脂(東洋紡)パイ
ロン200 15部トル
エン 40部メチルエチル
ケトン 40部B液を用いA液と同様にし
て実施例1.3、比較例1.3用の受像体を作成した。[Liquid B] Polyester resin (Toyobo) Pylon 200 15 parts Toluene 40 parts Methyl ethyl ketone 40 parts Using Liquid B, image receptors for Example 1.3 and Comparative Example 1.3 were prepared in the same manner as Liquid A.
次に実施例1.3、比較例1.3の転写体と前記受像体
を用いて印加電力442mW/dat、サーマルヘッド
Bdot/am部分グレーズ及び印加エネルギーLlO
ij/dotの条件で印字した結果、実施例1.3はイ
ンク層、受像層の融着は生じなかった。しかし、比較例
1.3は若干生じた。Next, using the transfer body and the image receptor of Example 1.3 and Comparative Example 1.3, an applied power of 442 mW/dat, a thermal head Bdot/am partial glaze, and an applied energy LlO
As a result of printing under the conditions of ij/dot, in Example 1.3, no fusion occurred between the ink layer and the image-receiving layer. However, in Comparative Example 1.3, a slight amount occurred.
又、実施例1.4、比較例1.4を上記エネルギー条件
で受像体と記録体の速度比n−7で記録を行った結果、
実施例2.4ではインク層受像層間に融着による走行不
良及びインク層の熱転写は生じなかったが、比較例2.
4ではインク層の熱転写が若干生じた。In addition, as a result of recording Example 1.4 and Comparative Example 1.4 under the above energy conditions and at a speed ratio of n-7 between the image receptor and the recording medium,
In Example 2.4, there was no running failure due to fusion between the ink layer and the image-receiving layer, and no thermal transfer of the ink layer occurred, but in Comparative Example 2.
In No. 4, some thermal transfer of the ink layer occurred.
次に各インク層を60”100時間、恒温槽中で保存後
記録し、非加熱部の地肌汚れを評価した結果を下表に示
す。Next, each ink layer was stored in a constant temperature bath for 60 inches and 100 hours, and then recorded, and the results of evaluating the background stain in the non-heated area are shown in the table below.
の画像を形成することができる。images can be formed.
Claims (1)
する昇華型熱転写体において、前記インク層中に結着剤
と反応する官能基を分子の片方の末端のみに有するポリ
ジメチルシロキサンを含有することを特徴とする昇華型
熱転写体。In a sublimation thermal transfer material having an ink layer on a substrate in which a sublimable dye is dispersed in a binder, the ink layer contains polydimethylsiloxane having a functional group that reacts with the binder at only one end of the molecule. A sublimation type thermal transfer material characterized by containing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2064065A JPH03266692A (en) | 1990-03-16 | 1990-03-16 | Sublimation type thermal transfer material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2064065A JPH03266692A (en) | 1990-03-16 | 1990-03-16 | Sublimation type thermal transfer material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03266692A true JPH03266692A (en) | 1991-11-27 |
Family
ID=13247321
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2064065A Pending JPH03266692A (en) | 1990-03-16 | 1990-03-16 | Sublimation type thermal transfer material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03266692A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7067457B2 (en) | 2003-09-17 | 2006-06-27 | Eastman Kodak Company | Thermal donor for high-speed printing |
US7135433B2 (en) | 2003-09-17 | 2006-11-14 | Eastman Kodak Company | Thermal print assembly |
JP2013107295A (en) * | 2011-11-21 | 2013-06-06 | Toyo Ink Sc Holdings Co Ltd | Sublimation transfer sheet |
-
1990
- 1990-03-16 JP JP2064065A patent/JPH03266692A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7067457B2 (en) | 2003-09-17 | 2006-06-27 | Eastman Kodak Company | Thermal donor for high-speed printing |
US7135433B2 (en) | 2003-09-17 | 2006-11-14 | Eastman Kodak Company | Thermal print assembly |
JP2013107295A (en) * | 2011-11-21 | 2013-06-06 | Toyo Ink Sc Holdings Co Ltd | Sublimation transfer sheet |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH0390385A (en) | Sublimation type thermal transfer image receiving medium | |
JPH03266692A (en) | Sublimation type thermal transfer material | |
JP2714670B2 (en) | Sublimation transfer recording method | |
JPH03121893A (en) | Sublimation type thermal transfer material | |
JPH0640171A (en) | Thermal transfer sheet | |
JPH09234963A (en) | Heat-sensitive transfer recording medium | |
JP2931008B2 (en) | Sublimation transfer image receiving medium | |
JP2926619B2 (en) | Sublimation transfer image receiving medium | |
JP2925210B2 (en) | Sublimation type thermal transfer method | |
JPH0624155A (en) | Image receiving sheet for sublimation type thermal transfer printing | |
JP2908801B2 (en) | Sublimation type thermal transfer image receiving medium | |
JP3081631B2 (en) | Sublimation thermal transfer image receiving medium | |
JP2925184B2 (en) | Sublimation type thermal transfer image receiving medium | |
JPH04163092A (en) | Thermal transfer recording medium | |
JPH03178484A (en) | Sublimable thermal transfer image receiving medium | |
JP2866871B2 (en) | Sublimation thermal transfer image receiving medium | |
JP2925171B2 (en) | Sublimation type thermal transfer image receiving medium | |
JPH03124493A (en) | Sublimation type thermal transfer body | |
JPH0516544A (en) | Sublimation thermal transfer image receiving medium | |
JPH03274190A (en) | Thermal transfer recording method | |
JPH0524369A (en) | Sublimable type thermal transfer recording medium and image receiving medium for said transfer | |
JPH03180392A (en) | Image receiving sheet for sublimation type thermal transfer | |
JPH02227291A (en) | Sublimable thermally transferrable recording medium | |
JPH0260791A (en) | Image receiving sheet for thermal transfer recording | |
JPH09175043A (en) | Sublimation type heat transfer body |