JPH01125287A - Thermal transfer recording material - Google Patents
Thermal transfer recording materialInfo
- Publication number
- JPH01125287A JPH01125287A JP62284602A JP28460287A JPH01125287A JP H01125287 A JPH01125287 A JP H01125287A JP 62284602 A JP62284602 A JP 62284602A JP 28460287 A JP28460287 A JP 28460287A JP H01125287 A JPH01125287 A JP H01125287A
- Authority
- JP
- Japan
- Prior art keywords
- foaming agent
- recording material
- thermal transfer
- ink layer
- transfer 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 29
- 239000004088 foaming agent Substances 0.000 claims abstract description 24
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 16
- 239000001282 iso-butane Substances 0.000 claims description 8
- 239000002775 capsule Substances 0.000 claims description 7
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 4
- 238000007639 printing Methods 0.000 abstract description 12
- 238000010438 heat treatment Methods 0.000 abstract description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 4
- 238000005187 foaming Methods 0.000 description 10
- 239000002245 particle Substances 0.000 description 8
- 239000004604 Blowing Agent Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000001993 wax Substances 0.000 description 7
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 6
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 6
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 6
- 239000005642 Oleic acid Substances 0.000 description 6
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 6
- 239000004203 carnauba wax Substances 0.000 description 6
- 235000013869 carnauba wax Nutrition 0.000 description 6
- 239000005038 ethylene vinyl acetate Substances 0.000 description 6
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- -1 azide compounds Chemical class 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000006261 foam material Substances 0.000 description 2
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 238000005979 thermal decomposition reaction 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
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/392—Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は熱転写性を改良した熱転写記録材に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to a thermal transfer recording material with improved thermal transfer properties.
近年、熱転写記録は、ノンインパクトで無騒音、メンテ
ナンスフリー、低コスト、小型軽量化可能、カラー化可
能等の特長を有する為にファクシミリ、コンピュータ一
端末、レコーダー等の多くの分野で用いられている。In recent years, thermal transfer recording has been used in many fields such as facsimiles, computer terminals, and recorders due to its features such as non-impact, noiseless, maintenance-free, low cost, size and weight, and color printing. .
このような熱転写記録方式は、サーマルヘッドで記録材
表面を昇温加熱するか、或いは通電ヘッドで通電発熱抵
抗層を昇温加熱する事でインク層が、記録紙上に溶融転
写するものである。In such a thermal transfer recording method, an ink layer is melted and transferred onto a recording paper by heating the surface of the recording material using a thermal head or by heating an energized heat-generating resistive layer using a current-carrying head.
だがこの方式にも幾つかの欠点があった。However, this method also had some drawbacks.
本熱転写記録方式の転写性は、転写紙に普通紙を用いた
場合、普通紙表面の凹凸、表面物性、インク層の接着力
、浸透性等に大きく影響される。When plain paper is used as the transfer paper, the transferability of this thermal transfer recording method is greatly influenced by the unevenness of the surface of the plain paper, the surface physical properties, the adhesive strength of the ink layer, the permeability, etc.
特に表面の凹凸の大きい紙の場合には印字時に熱溶融し
たインクが紙の繊維の中まで浸透できず、表面の凸部或
いはその近傍にのみ付着するため、印字された像のエツ
ジ部がシャープでなかったり、像の一部が欠けたりして
、印字品位を低下させることになる。また、印字品位の
向上のために、融点の低い熱溶融性バインダーを使用す
ることも考えられるが、この場合には、熱転写性インク
層が比較的低温においても粘着性をおび、ブロッキング
等の発生による保存性の低下ならびに記録材の非印字部
での汚損等の不都合を生ずる。Particularly in the case of paper with large surface irregularities, the hot melted ink cannot penetrate into the fibers of the paper during printing and only adheres to the convex parts of the surface or the vicinity thereof, resulting in sharp edges of the printed image. Otherwise, part of the image may be missing, resulting in a decrease in printing quality. In addition, in order to improve printing quality, it is possible to use a heat-melting binder with a low melting point, but in this case, the heat-transferable ink layer becomes sticky even at relatively low temperatures, causing blocking, etc. This causes inconveniences such as a decline in storage stability and staining of non-printing areas of the recording material.
上記問題を解決する為の手段として、例えば特開昭59
−201893に示される様に、熱分解性発泡剤をイン
ク層中に含有される技術が考案され、発泡剤の成分とし
ては重炭酸塩、炭酸塩、アジド化合物等の無機系発泡剤
及び、アゾ系、ニトロソ系、スルホニルヒドラジド系の
有機系発泡剤を用いる技術が公知であった。As a means to solve the above problem, for example,
-201893, a technology was devised in which a thermally decomposable blowing agent is contained in the ink layer, and the blowing agent components include inorganic blowing agents such as bicarbonate, carbonate, and azide compounds, and azo Techniques using organic blowing agents such as nitroso-based, nitroso-based, and sulfonyl hydrazide-based blowing agents have been known.
そこで本発明は、従来のこの様な問題点を解決する為、
低エネルギーで発泡性の良好な発泡剤をインク層中に含
有する事により、平滑性の低い記録紙に対しても印字品
位が良好でかつ発熱溶融特性の優れた熱転写記録材を得
ることを目的とじている。Therefore, in order to solve these conventional problems, the present invention
By containing a foaming agent with low energy and good foaming properties in the ink layer, the aim is to obtain a thermal transfer recording material that has good print quality even on recording paper with low smoothness and has excellent heat-generating melting properties. It is closed.
しかし、これらの発泡剤をインク層中に含有する熱転写
記録材を用いて印字した場合、加熱してから発泡する迄
の時間がかかり、高速印字が難しい、又所望の発泡量を
得る為には、高エネルギーが必要であるという欠点を有
していた。However, when printing with a thermal transfer recording material containing these foaming agents in the ink layer, it takes time for foaming to occur after heating, making high-speed printing difficult and difficult to obtain the desired amount of foaming. , which had the disadvantage of requiring high energy.
上記問題点を解決する為に、本発明の熱転写記録材は発
熱手段により、発泡材を成分とするインク層を溶融させ
、被記録紙に転写して記録を得る熱転写記録材において
、前記発泡材はイソブタンを内包しかつカプセル化され
る事を特徴とする。In order to solve the above problems, the thermal transfer recording material of the present invention melts an ink layer containing a foamed material using a heat generating means and transfers it to a recording paper to obtain a recording. is characterized by containing isobutane and being encapsulated.
さらには、前記発泡材のカプセル外皮破壊温度が55〜
280℃の範囲であることを特徴とする。Furthermore, the capsule outer skin breaking temperature of the foamed material is 55 to
It is characterized by a temperature range of 280°C.
さらには、前記発泡材がインク層中に0.1〜35重量
%含有されることを特徴とする。Furthermore, the ink layer contains the foaming material in an amount of 0.1 to 35% by weight.
以下に本発明の実施例を詳細に説明するが、本発明はこ
れに限定するものではない。本発明に用いた発泡材はイ
ソブタンを塩化ビニリデン/アクリロニトリルのコーポ
リマー中に内包、カプセル化したものを用いた。発泡材
のカプセル外皮破壊温度は55〜280℃の範囲内にあ
る事が必要で、好ましくは60〜150″Cの範囲が良
い。該温度が55℃未満では、インク層を構成するワッ
クスや樹脂の軟化溶融温度もほぼ同等以下と低い物性値
を持つ物質を選定しなければならず、そうすると、保存
性が低下しブロッキングが生じやすい。Examples of the present invention will be described in detail below, but the present invention is not limited thereto. The foam material used in the present invention was one in which isobutane was encapsulated and encapsulated in a vinylidene chloride/acrylonitrile copolymer. The capsule shell breaking temperature of the foam material must be within the range of 55 to 280°C, preferably 60 to 150''C. If the temperature is less than 55°C, wax and resin constituting the ink layer will be destroyed. It is necessary to select a material that has low physical properties, such as a softening and melting temperature that is approximately equal to or lower than that of , which reduces storage stability and tends to cause blocking.
他方該温度が280℃を越えると、発泡性が低下し転写
性の低下につながる。On the other hand, if the temperature exceeds 280°C, the foaming properties will be reduced, leading to a reduction in the transferability.
又、発泡剤の含有量としては、O,1〜35重量%が適
当である。含有量が低いと発泡量が少なくなり、普通紙
への転写性が劣り、対して含有量が多いと他のインク組
成の含有量が減少することになり、転写性が低下しボイ
ドが発生し易(なる。Further, the content of the blowing agent is suitably 1 to 35% by weight of O. If the content is low, the amount of foaming will be small, resulting in poor transferability to plain paper, whereas if the content is high, the content of other ink compositions will be reduced, resulting in poor transferability and the generation of voids. It becomes easy.
〔実施例−1]
第1図に示した如く、発泡剤3を含有したインク層2を
有する熱転写記録材を作成した。支持体1としては厚さ
約6μmのポリエチレンテレフタレートフィルムを用い
た。又、インク層2の組成は以下の様に調整し、溶剤中
に分散し、ワイヤーバーを用いて乾燥後の厚みが12μ
m程度になる様塗工した。[Example 1] As shown in FIG. 1, a thermal transfer recording material having an ink layer 2 containing a foaming agent 3 was prepared. As the support 1, a polyethylene terephthalate film having a thickness of about 6 μm was used. The composition of the ink layer 2 was adjusted as follows, dispersed in a solvent, and dried using a wire bar to a thickness of 12 μm.
It was coated to a thickness of about m.
インク −〇カルナバワック
ス 30
パラフインワツクス 25
(m、 p、 60〜62℃)
オレイン酸 5工チレン酢ビ共
重合体 10
サーポンプラツク 20
発泡剤 10
尚、発泡剤3のカプセル外皮破壊温度は70〜100℃
の範囲であり、平均粒径が10μm、発泡後の平均粒径
が40μmになる、イソブタンを内包するものを用いた
。Ink - Carnauba wax 30 Parafine wax 25 (m, p, 60 to 62°C) Oleic acid 5-functional ethylene-vinyl acetate copolymer 10 Surpon plug 20 Foaming agent 10 The capsule shell breaking temperature of Foaming agent 3 is 70 ~100℃
A material containing isobutane with an average particle diameter of 10 μm and an average particle diameter of 40 μm after foaming was used.
〔実施例−2〕
下記の組成を、溶剤中に分散してインクを作成実施例1
と同様に、乾燥後のインクN2の厚みが約12μmにな
る様支持体1上に塗工した。[Example-2] Ink was prepared by dispersing the following composition in a solvent Example 1
Similarly, the ink N2 was coated on the support 1 so that the thickness after drying was about 12 μm.
インク −0カルナバワツク
ス 35
パラフインワツクス 29.9オレイン酸
5工チレン酢ビ共重合体
10
サーポンプランク 20発泡剤
0.1尚、発泡剤3のカプセル外皮
破壊温度は70〜100℃の範囲であり、平均粒径が1
0am、発泡後の平均粒径が40μmになる、イソブタ
ンを内包するものを用いた。Ink -0 Carnauba wax 35 Parafine wax 29.9 Oleic acid 5-functional ethylene vinyl acetate copolymer
10 Surpon crank 20 Foaming agent
0.1 The capsule shell breaking temperature of the foaming agent 3 is in the range of 70 to 100°C, and the average particle size is 1.
0 am, the average particle size after foaming was 40 μm, and one containing isobutane was used.
〔実施例−3]
下記の組成を、溶剤中に分散してインクを作成実施例1
と同様に、乾燥後のインク層2の厚みが約12μmにな
る様支持体1上に塗工した。[Example-3] Create ink by dispersing the following composition in a solvent Example 1
In the same manner as above, the ink layer 2 was coated on the support 1 so that the thickness of the ink layer 2 after drying was about 12 μm.
インク −0カルナバワツク
ス 20
パラフインワツクス 20
オレイン酸 3工チレン酢ビ共
重合体 7
サーボンブラツク 15発−泡剤
35尚、発泡剤3のカプセル外皮
破壊温度は70〜100℃の範囲であり、平均粒径が1
0μm、発泡後の平均粒径が40μmになる、イソブタ
ンを内包するものを用いた。Ink -0 Carnauba wax 20 Parafine wax 20 Oleic acid 3-engineered ethylene vinyl acetate copolymer 7 Servon black 15 Foaming agent
35 The capsule shell breaking temperature of the foaming agent 3 is in the range of 70 to 100°C, and the average particle size is 1.
A material containing isobutane with an average particle size of 0 μm and 40 μm after foaming was used.
〔比較例−1]
支持体1として厚さ6μmのポリエチレンテレフタレー
トフィルムを用い、インク層2の組成ヲ下記の様に調整
し溶剤中に分散、ワイヤーバーを用いて乾燥後の厚みが
約12μmになる様に塗工した。[Comparative Example-1] A polyethylene terephthalate film with a thickness of 6 μm was used as the support 1, and the composition of the ink layer 2 was adjusted as shown below, dispersed in a solvent, and dried using a wire bar to a thickness of about 12 μm. I painted it to look like this.
インク −〇カルナバワック
ス 30
パラフインワツクス 30
オレイン酸 5工チレン酢ビ共
重合体 15
サーボンブラツク 20
上記方法により作成した熱転写記録材を第2図に示す。Ink - Carnauba wax 30 Parafine wax 30 Oleic acid 5-functional ethylene-vinyl acetate copolymer 15 Servon black 20 The thermal transfer recording material prepared by the above method is shown in FIG.
〔比較例−2]
下記の組成を、溶剤中に分散してインクを作成支持体l
上にワイヤーバーを用いて乾燥後のインク層2の厚みが
約12μmになる様に塗工した。[Comparative Example-2] Ink was prepared by dispersing the following composition in a solvent.
The ink layer 2 was coated on top using a wire bar so that the thickness of the ink layer 2 after drying was about 12 μm.
イン 0
カルナバワツクス 20
パラフインワツクス 15
オレイン酸 3工チレン酢ビ共
重合体 7
サーボンブラツク 15
発泡剤 40
尚、発泡剤3のカプセル外皮破壊温度は70〜100℃
の範囲であり、平均粒径が10μm、発泡後の平均粒径
が40μmになる。イソブタンを内包するものを用いた
。In 0 Carnauba wax 20 Parafine wax 15 Oleic acid 3-engineered ethylene-vinyl acetate copolymer 7 Servon black 15 Foaming agent 40 The capsule shell breaking temperature of Foaming agent 3 is 70 to 100°C
The average particle size is 10 μm, and the average particle size after foaming is 40 μm. I used one that contained isobutane.
〔比較例−3〕
下記の組成を、溶剤中に分散してインクを作成支持体1
上にワイヤーバーを用いて乾燥後のインク層2の厚みが
約12μmになる様塗工した。[Comparative Example-3] Ink was prepared by dispersing the following composition in a solvent Support 1
The ink layer 2 was coated on top using a wire bar so that the thickness of the ink layer 2 after drying was about 12 μm.
インク Oカルナバワック
ス 30
パラフインワツクス 25
オレイン酸 5工チレン酢ビ共
重合体 10
サーポンプラツク 20
発泡剤 10
尚、上記発泡剤は、炭酸アンモニウムを主成分とするも
のを用いた。Ink: O carnauba wax 30 Parafine wax 25 Oleic acid 5-functional ethylene-vinyl acetate copolymer 10 Surpon plug 20 Foaming agent 10 The above-mentioned foaming agent was one containing ammonium carbonate as a main component.
以上の如く得た、熱転写記録材をベック平滑度の異なる
下記2種の記録紙にサーマルプリンタにて印字を行い、
印字品位を目視にて評価した。尚、印字速度は40cp
s及び80cps、ヘッド電圧は18V及び25Vとし
た。The thermal transfer recording material obtained as described above was printed on the following two types of recording paper with different Beck smoothness using a thermal printer.
Print quality was visually evaluated. Furthermore, the printing speed is 40cp.
s and 80 cps, and head voltages were 18V and 25V.
晋、 べ・・ パ(secランカスタ
ーボンド紙 6〜8ゼロツクス4024
25〜30評価結果を第1表に示す。Shin, Be... Pa (sec Lancaster Bond Paper 6~8 Xerox 4024
25-30 evaluation results are shown in Table 1.
−第1表−
注)O1Δ、×は良から不良に段階的に変化する評価で
ある。-Table 1- Note) O1Δ, × are evaluations that change stepwise from good to bad.
以上の結果から明らかな如く、本発明の実施例にかかる
熱転写記録材を用いる事により平滑性の低い記録紙上に
低エネルギー、高速印字の条件でも印字品質の良好な転
写を得ることができた。As is clear from the above results, by using the thermal transfer recording material according to the example of the present invention, it was possible to obtain transfer with good print quality on recording paper with low smoothness even under low energy and high speed printing conditions.
又、第3図は本発明に於ける熱転写記録材を凹凸のある
転写紙に転写した図である。図より解かるように、サー
マルヘッド4により加熱されたインク層2中の発泡剤3
は熱分解膨張し、転写紙5上の凹凸の表面に効率よく接
触する。支持体1を転写紙5から引き剥がすと転写紙5
上に加熱溶融されたインク6が転写される。Further, FIG. 3 is a diagram showing the thermal transfer recording material of the present invention transferred onto a transfer paper having unevenness. As can be seen from the figure, the foaming agent 3 in the ink layer 2 heated by the thermal head 4
expands due to thermal decomposition and efficiently contacts the uneven surface of the transfer paper 5. When the support 1 is peeled off from the transfer paper 5, the transfer paper 5
The heated and melted ink 6 is transferred onto the surface.
本発明は以上説明した様に、イソブタンを内包し、かつ
カプセル化した発泡剤をインク層中に含有する熱転写記
録剤を用いる事により、平滑性の低い記録紙上に低エネ
ルギー、高速印字の条件でも印字品位の良好な発熱特性
の優れた熱転写記録材を得ることができるものである。As explained above, the present invention uses a thermal transfer recording material containing isobutane and an encapsulated foaming agent in the ink layer, so that it can be printed even under low energy and high speed printing conditions on recording paper with low smoothness. A thermal transfer recording material with good print quality and excellent heat generation properties can be obtained.
第1図は、本発明の熱転写記録材の断面図を示す。第2
図は比較例を示す図である。第3図は本発明の転写紙に
熱転写記録材を転写する状態を示す図である。
1・・・支持体
2・・・インク層
3・・・発泡剤
4・・・サーマルヘッド
5・・・転写紙
6・・・加熱溶融されたインク
7・・・プラテン
以上
出願人 セイコーエプソン株式会社
第1図
第2図FIG. 1 shows a cross-sectional view of the thermal transfer recording material of the present invention. Second
The figure shows a comparative example. FIG. 3 is a diagram showing a state in which a thermal transfer recording material is transferred to a transfer paper of the present invention. 1...Support 2...Ink layer 3...Blowing agent 4...Thermal head 5...Transfer paper 6...Heat-melted ink 7...Platen and above Applicant Seiko Epson Corporation Company Figure 1 Figure 2
Claims (3)
溶融させ、被記録紙に転写して記録を得る熱転写記録材
において、前記発泡剤はイソブタンを内包し且つカプセ
ル化されて成る事を特徴とする熱転写記録材。(1) In a thermal transfer recording material in which a recording is obtained by melting an ink layer containing a foaming agent as a component using a heat generating means and transferring it to recording paper, the foaming agent includes isobutane and is encapsulated. Features of thermal transfer recording material.
0℃の範囲である事を特徴とする特許請求の範囲第1項
記載の熱転写記録材。(2) The capsule shell breaking temperature of the foaming agent is 55 to 28
The thermal transfer recording material according to claim 1, characterized in that the temperature is in the range of 0°C.
有されることを特徴とする特許請求の範囲第1項記載の
熱転写記録材。(3) The thermal transfer recording material according to claim 1, wherein the foaming agent is contained in the ink layer in an amount of 0.1 to 35% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62284602A JPH01125287A (en) | 1987-11-11 | 1987-11-11 | Thermal transfer recording material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62284602A JPH01125287A (en) | 1987-11-11 | 1987-11-11 | Thermal transfer recording material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01125287A true JPH01125287A (en) | 1989-05-17 |
Family
ID=17680581
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62284602A Pending JPH01125287A (en) | 1987-11-11 | 1987-11-11 | Thermal transfer recording material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01125287A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1314575A3 (en) * | 1990-09-07 | 2003-09-17 | Dai Nippon Printing Co., Ltd. | Thermal transfer image receiving sheet and thermal transfer sheet |
-
1987
- 1987-11-11 JP JP62284602A patent/JPH01125287A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1314575A3 (en) * | 1990-09-07 | 2003-09-17 | Dai Nippon Printing Co., Ltd. | Thermal transfer image receiving sheet and thermal transfer sheet |
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