JP2699333B2 - Method for producing transfer body for thermal transfer recording - Google Patents
Method for producing transfer body for thermal transfer recordingInfo
- Publication number
- JP2699333B2 JP2699333B2 JP61300972A JP30097286A JP2699333B2 JP 2699333 B2 JP2699333 B2 JP 2699333B2 JP 61300972 A JP61300972 A JP 61300972A JP 30097286 A JP30097286 A JP 30097286A JP 2699333 B2 JP2699333 B2 JP 2699333B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- transfer body
- weight
- parts
- recording
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229920005989 resin Polymers 0.000 claims description 31
- 239000011347 resin Substances 0.000 claims description 31
- 239000000463 material Substances 0.000 claims description 23
- 239000000758 substrate Substances 0.000 claims description 15
- 239000011230 binding agent Substances 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 229920000515 polycarbonate Polymers 0.000 claims description 3
- 239000004417 polycarbonate Substances 0.000 claims description 3
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 229920006230 thermoplastic polyester resin Polymers 0.000 claims 1
- 229920001225 polyester resin Polymers 0.000 description 13
- 239000004645 polyester resin Substances 0.000 description 12
- 239000000975 dye Substances 0.000 description 8
- 230000004927 fusion Effects 0.000 description 8
- 239000000976 ink Substances 0.000 description 8
- -1 for example Polymers 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 229920002492 poly(sulfone) Polymers 0.000 description 4
- 238000000859 sublimation Methods 0.000 description 4
- 230000008022 sublimation Effects 0.000 description 4
- 229920002799 BoPET Polymers 0.000 description 3
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 239000002390 adhesive tape Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920006015 heat resistant resin Polymers 0.000 description 2
- 229920006290 polyethylene naphthalate film Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 229920001634 Copolyester Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001230 polyarylate Polymers 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
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; 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
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、昇華型感熱転写記録に用いられる転写体の
製造方法に関する。
従来の技術
昇華型転写体の結着剤に求められる基本特性は、基剤
と色材層の接着性を向上させること、又、熱転写記録時
に転写体の色材層と受像紙(記録紙)間の融着を防ぐこ
と等である。
従来、結着剤として架橋性樹脂,ポリエステル系樹
脂,セルロース系樹脂等多数の樹脂が提案されている。
(例えば、特開昭58-215397号公報)
発明が解決しようとする問題点
従来提案されている結着剤はほとんど熱転写記録時の
融着を防止するために耐熱性の高い樹脂あるいは架橋性
樹脂であり、又、基剤との密着性のよいポリエステル系
樹脂である。耐熱性の高い樹脂は熱融着を防止するが、
特に低濃度域の記録濃度が低い。ポリエステル系樹脂は
基材との密着性はよいが高熱エネルギー域で熱融着を発
生しやすい等の問題点がある。
本発明は受像紙との熱融着がなく特に低濃度域におい
て記録濃度が高く、又、基材と色材層間との密着性のよ
い転写体の製造方法を得ることを目的とする。
問題点を解決するための手段
100℃以上の熱変形温度を有する有機溶媒可溶性樹脂
(A樹脂)と、有機溶媒可溶性の熱可塑性共重合ポリエ
ステル樹脂(B樹脂)と、昇華型色素と、有機溶媒とか
らなるインキにおいて、前記A樹脂と前記B樹脂との配
合合計量100重量部中における前記A樹脂の配合割合が1
0〜90重量部であり、前記B樹脂の配合割合が90〜10重
量部である前記インキを基材上に塗工して、前記A樹脂
と前記B樹脂とからなる結着剤と、前記昇華型色素とか
ら構成されている色材層を基材上に有する感熱転写記録
用転写体の製造方法と、更に、前記A樹脂がポリサルホ
ン、ポリカーボネート及びポリフェニレンオキサイドか
ら選択される少なくとも一種から構成される感熱転写記
録用転写体の製造方法である。
作用
100℃以上の熱変形温度を有する樹脂は、高熱エネル
ギー部での熱融着を防止する。共重合ポリエステル樹脂
は、基材との密着性を保持し、又低濃度域(低エネルギ
ー域)において柔軟性を示すため、色材層と受像体とが
密着しやすくなり高記録濃度が得られる。
実施例
第1図に本発明の実施例である転写体断面模式図を示
す。基材1の片面に色材層2がある。色材層2は少なく
とも色素3と結着剤4とから構成されている。
基材1としては各種基材を用いることができ特に限定
されるものでない。一般的にはポリエステル系フィル
ム、例えばポリエチレンテレフタレートフィルム,ポリ
エチレンナフタレートフィルムおよびこれらのフィルム
にサーマルヘッドに対する走行安定性を付加加工したも
の、あるいはさらに耐熱性の優れた各種フィルム等を用
いることができる。又、基材自身に導電性を付与したも
の、あるいは基材の少なくとも片面に導電性を付与した
ものでもよい。これらの基材は、例えば通電ヘッドを用
いた感熱転写記録に主に利用できる。
色素は、分散染料,塩基性染料等の昇華型感熱転写記
録方法に利用できる染料であれば特に限定されるもので
はない。
結着剤は、100℃以上の熱変形温度を有する樹脂と共
重合ポリエステル樹脂とから少なくとも構成されてい
る。
ここで熱変形温度は、アメリカ材料試験協会の試験方
法(ASTM,D648,荷重18.6Kg/cm2)によって決定される温
度である。
100℃以上の熱変形温度を有する樹脂として、例えば
ポリサルホン,ポリカーボネイト,ポリフェニレンオキ
サイド,ポリアリレート等がある。
特に120℃以上の熱変形温度を有する樹脂が良好であ
る。
熱可塑性共重合ポリエステル樹脂として、例えばバイ
ロン(商品名,東洋紡績株式会社),ポリエスター(商
品名,日本合成化学工業株式会社)等を利用できる。
共重合ポリエステル樹脂は、イソシアネート化合物、
エポキシ樹脂,メラミン樹脂,フェノール樹脂等の硬化
剤との組合せにより反応生成物を形成していてもよい。
100℃以上の熱変形温度を有する樹脂と共重合ポリエス
テル樹脂との混合比率は、前者が10〜90重量部,後者が
90〜10重量部の範囲で混合効果が大きい。結着剤は100
℃以上の熱変形温度を有する樹脂と共重合ポリエステル
樹脂との混合物、あるいは反応物でもよい。又、100℃
以上の熱変形温度を有する樹脂と共重合ポリエステル樹
脂とが非相溶である場合、良好な特性を示す。
色材層は色素と結着剤以外に界面活性剤,離型剤,微
粒子等が添加されていてもよい。
以下、具体的実施例を示す。
(実施例)
裏面に滑性耐熱層を有する6μmのPETフィルムの表
面に下記組成のインキをワイヤーバーで塗工して転写体
を得た。
〈インキ〉
下記構造式(A)の色素 1.5重量部
ポリサルホン(P−1700,熱変形温度:175℃,日産化学
工業株式会社) 2.0重量部
共重合ポリエステル樹脂(バイロン220,東洋紡績株式会
社) 2.0重量部
モノクロルベンゼン 100重量部
次にポリプロピレン系合成紙の片面に水性ポリエステ
ル樹脂(MD1200,東洋紡績株式会社)25重量部、コロイ
ダルシリカ(固形分40wt%)40重量部,ポリエチレンエ
マルジョン(固形分20wt%)20重量部からなる水性塗料
をワイヤーバで塗工して厚さ約5μmの染着層を有する
受像紙を得た。
以下、下記の条件で熱転写記録した。
主及び副走査のドット密度: 6ドット/mm
記録電力 : 0.5W/ドット
ヘッドの加熱時間 : 2〜8ms
記録後、受像紙との熱融着はまったくなく又、受像紙
表面からのカラーシートの剥離も容易であった。得られ
た記録濃度曲線を第2図に示す。又基材と色材層間の密
着性は幅12mmの接着テープ(ニチバン)を色材層上に10
0mmの長さで接着させた後、等速度(1cm/秒)で剥離し
て試験した。その結果、色材層はまったく基材から剥離
しなかった。
(比較例)
実施例と同一のPETフィルムの表面に下記組成のイン
キをワイヤーバーで塗工して転写体を得た。この転写体
を転写体Aとする。
〈インキ〉
実施例で用いた色素 1.5重量部
ポリサルホン 4.0 〃
モノクロルベンゼン 100 〃
又、実施例と同一のPETフィルムの表面に下記組成のイ
ンキをワイヤーバーで塗工して転写体を得た。この転写
体を転写体Bとする。
〈インキ〉
実施例で用いた色素 1.5重量部
共重合ポリエステル樹脂(バイロン220) 4.0 〃
モノクロルベンゼン 100 〃
上記転写体A及びBについて実施例と同一の受像紙,
記録条件で記録した。
その結果、転写体Aは受像紙と熱融着を発生しなかっ
たが、転写体Bは7msから受像紙と熱融着を発生した。
転写体Aにより得られた記録濃度曲線を第2図に示す。
転写体Aの基材と色材層間の密着性はたいへん悪く接着
テープの接着面のほぼ全面が容易に剥離した。
発明の効果
本発明によれば、受像紙との熱融着がなく特に低濃度
域において記録濃度が高く、又、基材と色材層間との密
着性のよい転写体が得られる。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a transfer member used for sublimation-type thermal transfer recording. 2. Description of the Related Art The basic characteristics required for a binder of a sublimation type transfer body are to improve the adhesiveness between a base material and a color material layer, and to make the transfer material color material layer and image receiving paper (recording paper) in thermal transfer recording. And to prevent fusion between them. Conventionally, many resins such as a crosslinkable resin, a polyester resin, and a cellulose resin have been proposed as a binder.
(For example, Japanese Patent Application Laid-Open No. 58-215397) Problems to be Solved by the Invention Conventionally, binders that have been conventionally proposed are almost heat-resistant resins or crosslinkable resins in order to prevent fusion during thermal transfer recording. And a polyester resin having good adhesion to the base. High heat resistant resin prevents heat fusion,
In particular, the recording density in the low density range is low. Polyester-based resins have good adhesion to the base material, but have problems such as that heat fusion easily occurs in a high heat energy region. SUMMARY OF THE INVENTION It is an object of the present invention to provide a method for producing a transfer body which is free from heat fusion with an image receiving paper, has a high recording density particularly in a low density region, and has good adhesion between a substrate and a color material layer. Means for Solving the Problems An organic solvent-soluble resin (A resin) having a heat distortion temperature of 100 ° C. or higher, a thermoplastic copolymer polyester resin (B resin) soluble in an organic solvent, a sublimation dye, and an organic solvent In the ink consisting of: the mixing ratio of the resin A is 1 in 100 parts by weight of the total amount of the resin A and the resin B;
0 to 90 parts by weight, the blending ratio of the B resin is 90 to 10 parts by weight of the ink is applied on a substrate, the binder comprising the A resin and the B resin, A method for producing a thermal transfer recording transfer body having a coloring material layer composed of a sublimation type dye on a base material, and further, the A resin is composed of at least one selected from polysulfone, polycarbonate and polyphenylene oxide. This is a method for producing a transfer body for thermal transfer recording. Action A resin having a heat distortion temperature of 100 ° C. or more prevents heat fusion in a high heat energy part. The copolyester resin maintains adhesion to the substrate and exhibits flexibility in a low concentration range (low energy range), so that the color material layer and the image receiving body are easily adhered to each other, and a high recording density is obtained. . Embodiment FIG. 1 is a schematic cross-sectional view of a transfer body according to an embodiment of the present invention. A color material layer 2 is provided on one side of the substrate 1. The color material layer 2 includes at least a dye 3 and a binder 4. As the substrate 1, various substrates can be used and are not particularly limited. In general, polyester films, for example, polyethylene terephthalate film, polyethylene naphthalate film, and films obtained by adding running stability to a thermal head to these films, or various films having more excellent heat resistance can be used. Further, a substrate having conductivity imparted to itself or a substrate having conductivity imparted to at least one surface of the substrate may be used. These substrates can be mainly used, for example, for thermal transfer recording using a current-carrying head. The dye is not particularly limited as long as it can be used in a sublimation type thermal transfer recording method such as a disperse dye or a basic dye. The binder is at least composed of a resin having a heat distortion temperature of 100 ° C. or higher and a copolymerized polyester resin. Here, the heat distortion temperature is a temperature determined by the test method of the American Society for Testing and Materials (ASTM, D648, load 18.6 kg / cm 2 ). Examples of the resin having a heat deformation temperature of 100 ° C. or higher include polysulfone, polycarbonate, polyphenylene oxide, and polyarylate. Particularly, a resin having a heat distortion temperature of 120 ° C. or more is preferable. As the thermoplastic copolymer polyester resin, for example, Byron (trade name, Toyobo Co., Ltd.), Polyester (trade name, Nippon Synthetic Chemical Industry Co., Ltd.) or the like can be used. The copolymerized polyester resin is an isocyanate compound,
The reaction product may be formed by a combination with a curing agent such as an epoxy resin, a melamine resin, and a phenol resin.
The mixing ratio of the resin having a heat distortion temperature of 100 ° C. or more and the copolymerized polyester resin is 10 to 90 parts by weight for the former and 10 for the latter for the latter.
The mixing effect is large in the range of 90 to 10 parts by weight. 100 binder
It may be a mixture of a resin having a heat distortion temperature of not less than ° C and a copolymerized polyester resin, or a reaction product. Also, 100 ℃
When the resin having the above heat distortion temperature and the copolymerized polyester resin are incompatible, good characteristics are exhibited. The coloring material layer may contain a surfactant, a release agent, fine particles and the like in addition to the dye and the binder. Hereinafter, specific examples will be described. Example A 6 μm PET film having a slippery heat-resistant layer on the back surface was coated with an ink having the following composition by a wire bar to obtain a transfer body. <Ink> Dye of the following structural formula (A) 1.5 parts by weight polysulfone (P-1700, heat distortion temperature: 175 ° C, Nissan Chemical Industries, Ltd.) 2.0 parts by weight Copolymerized polyester resin (Byron 220, Toyobo Co., Ltd.) 2.0 Parts by weight monochlorobenzene 100 parts by weight Next, an aqueous polyester resin (MD1200, Toyobo Co., Ltd.) 25 parts by weight, colloidal silica (solids 40 wt%) 40 parts by weight, polyethylene emulsion (solids 20 wt%) 20 parts by weight on one side of polypropylene synthetic paper The coating material was applied with a wire bar to obtain an image receiving paper having a dyeing layer having a thickness of about 5 μm. Hereinafter, thermal transfer recording was performed under the following conditions. Dot density for main and sub scanning: 6 dots / mm Recording power: 0.5 W / Dot head heating time: 2 to 8 ms After recording, there is no thermal fusion with the receiving paper and the color sheet from the receiving paper surface Peeling was also easy. FIG. 2 shows the obtained recording density curve. Also, the adhesion between the base material and the color material layer is as follows: Adhesive tape (Nichiban) with a width of 12 mm
After bonding at a length of 0 mm, the film was peeled off at a constant speed (1 cm / sec) and tested. As a result, the coloring material layer did not peel off from the substrate at all. (Comparative Example) An ink having the following composition was applied to the surface of the same PET film as in the example using a wire bar to obtain a transfer body. This transfer body is designated as transfer body A. <Ink> Dye 1.5 parts by weight polysulfone 4.0 {monochlorobenzene 100} used in the examples Inks having the following composition were coated on the surface of the same PET film as in the examples using a wire bar to obtain a transfer body. This transfer body is designated as transfer body B. <Ink> 1.5 parts by weight of pigment used in the examples Copolymerized polyester resin (Vylon 220) 4.0 〃 Monochlorobenzene 100 に つ い て The same image-receiving paper as that of the examples for the transfer members A and B,
Recording was performed under recording conditions. As a result, the transfer body A did not thermally fuse with the image receiving paper, but the transfer body B thermally fused with the image receiving paper from 7 ms.
FIG. 2 shows a recording density curve obtained by the transfer body A.
The adhesion between the base material of the transfer body A and the colorant layer was very poor, and almost the entire adhesive surface of the adhesive tape was easily peeled off. Effects of the Invention According to the present invention, it is possible to obtain a transfer body which has no thermal fusion with an image receiving paper, has a high recording density especially in a low density region, and has good adhesion between a substrate and a color material layer.
【図面の簡単な説明】
第1図は本発明の実施例として示した転写体の断面模式
図であり、第2図は本発明における実施例及び比較例と
して得られた記録濃度曲線図である。
1……基材、2……色材層、3……色素、4……結着
剤。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic cross-sectional view of a transfer body shown as an example of the present invention, and FIG. 2 is a recording density curve diagram obtained as an example and a comparative example in the present invention. . 1 ... substrate, 2 ... color material layer, 3 ... dye, 4 ... binder.
フロントページの続き (56)参考文献 特開 昭60−190389(JP,A) 特開 昭59−14994(JP,A) 特開 昭61−189994(JP,A) 特開 昭61−188193(JP,A) 特開 昭61−116583(JP,A) 特開 昭61−286199(JP,A)Continuation of front page (56) References JP-A-60-190389 (JP, A) JP-A-59-14994 (JP, A) JP-A-61-189994 (JP, A) JP-A-61-188193 (JP, A) JP-A-61-116583 (JP, A) JP-A-61-286199 (JP, A)
Claims (1)
て、100℃以上の熱変形温度を有する有機溶媒可溶性樹
脂(A樹脂)と、有機溶媒可溶性の熱可塑性共重合ポリ
エステル樹脂(B樹脂)と、昇華性色素と、有機溶媒と
から成り、且つ前記A樹脂と前記B樹脂との配合割合が
前記両樹脂の合計量を100重量部とした場合に前記A樹
脂が10〜90重量部であり、前記B樹脂が90〜10重量部で
ある色材層形成用インキを用い、前記インキを基材上に
塗工して、基材上に前記A樹脂と前記B樹脂とから成る
結着剤と、前記昇華性色素とから構成されている色材層
を形成する感熱転写記録用転写体の製造方法。 2.前記A樹脂がポリカーボネート及びポリフェニレン
オキサイドから選択される少なくとも一種である特許請
求の範囲第1項記載の感熱転写記録用転写体の製造法方
法。(57) [Claims] In a method for producing a transfer body having a color material layer on a base material, an organic solvent-soluble resin (A resin) having a heat distortion temperature of 100 ° C. or more, and an organic solvent-soluble thermoplastic polyester resin (B resin) A, comprising a sublimable dye and an organic solvent, and wherein the mixing ratio of the A resin and the B resin is 10 to 90 parts by weight when the total amount of both resins is 100 parts by weight. Using a colorant layer forming ink in which the B resin is 90 to 10 parts by weight, applying the ink on a substrate, and forming a binder comprising the A resin and the B resin on the substrate. And a method for producing a transfer body for thermal transfer recording, in which a color material layer composed of the above-mentioned sublimable dye is formed. 2. 2. The method according to claim 1, wherein the resin A is at least one selected from polycarbonate and polyphenylene oxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61300972A JP2699333B2 (en) | 1986-12-17 | 1986-12-17 | Method for producing transfer body for thermal transfer recording |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61300972A JP2699333B2 (en) | 1986-12-17 | 1986-12-17 | Method for producing transfer body for thermal transfer recording |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63153188A JPS63153188A (en) | 1988-06-25 |
JP2699333B2 true JP2699333B2 (en) | 1998-01-19 |
Family
ID=17891292
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61300972A Expired - Lifetime JP2699333B2 (en) | 1986-12-17 | 1986-12-17 | Method for producing transfer body for thermal transfer recording |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2699333B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2671545B2 (en) * | 1990-02-21 | 1997-10-29 | 松下電器産業株式会社 | Thermal transfer medium for multiple recordings |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5914994A (en) * | 1982-07-16 | 1984-01-25 | Matsushita Electric Ind Co Ltd | Image transfer element |
JPS60190389A (en) * | 1984-03-13 | 1985-09-27 | Mitsubishi Chem Ind Ltd | Sheet for heat transfer color recording |
JPS61116583A (en) * | 1984-11-12 | 1986-06-04 | Mitsubishi Paper Mills Ltd | Sublimation transfer type diazo thermal recording material |
JPS61188193A (en) * | 1985-02-15 | 1986-08-21 | Hitachi Ltd | thermal transfer paper |
JPS61189994A (en) * | 1985-02-20 | 1986-08-23 | Hitachi Ltd | thermal transfer paper |
JPS61286199A (en) * | 1985-06-13 | 1986-12-16 | Nippon Kogaku Kk <Nikon> | Sublimation transfer recording material |
-
1986
- 1986-12-17 JP JP61300972A patent/JP2699333B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS63153188A (en) | 1988-06-25 |
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