JPS62183384A - Thermal transfer recording medium - Google Patents
Thermal transfer recording mediumInfo
- Publication number
- JPS62183384A JPS62183384A JP61025069A JP2506986A JPS62183384A JP S62183384 A JPS62183384 A JP S62183384A JP 61025069 A JP61025069 A JP 61025069A JP 2506986 A JP2506986 A JP 2506986A JP S62183384 A JPS62183384 A JP S62183384A
- Authority
- JP
- Japan
- Prior art keywords
- paper
- layer
- layers
- transfer recording
- thermoplastic layer
- 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
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- 229920001721 polyimide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- JUVIOZPCNVVQFO-HBGVWJBISA-N rotenone Chemical compound O([C@H](CC1=C2O3)C(C)=C)C1=CC=C2C(=O)[C@@H]1[C@H]3COC2=C1C=C(OC)C(OC)=C2 JUVIOZPCNVVQFO-HBGVWJBISA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000012176 shellac wax Substances 0.000 description 1
- MXNUCYGENRZCBO-UHFFFAOYSA-M sodium;ethene;2-methylprop-2-enoate Chemical compound [Na+].C=C.CC(=C)C([O-])=O MXNUCYGENRZCBO-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 235000019385 spermaceti wax Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000007651 thermal printing Methods 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 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
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/423—Intermediate, backcoat, or covering layers characterised by non-macromolecular compounds, e.g. waxes
-
- 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
-
- 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
- B41M5/395—Macromolecular additives, e.g. binders
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
本発明は感熱転写記録媒体に関し、詳しくは表面平滑度
の低いう7ペーパーは勿論、表面平滑度の高い紙にも高
濃度かつ高品質で印字ができ、地汚れがなく、シかもブ
ロッキング耐性に優れた感熱転写記録媒体に関する。The present invention relates to a thermal transfer recording medium, and more specifically, it is capable of printing with high density and quality not only on papers with low surface smoothness, but also on paper with high surface smoothness, without background smudges, and with resistance to stain and blocking. Concerning an excellent thermal transfer recording medium.
熱転写記録法では熱転写受像紙の表面性が、画像に大き
な彩管をすえろことが知られている6例えば、受像紙(
紙)の表面平滑度が小さくなると四部にインクが入らな
くなり、転写確立が小さくなる(画像がボンついてくる
)。
この欠点を改良するには、熱軟化性のインクが加熱され
た場合の流動性を増す(流れ易くする)ので有効である
が、そのようなインクは、その軟化点をある程度低くす
る必要があった。
現在、インクの軟化点は60〜80℃のものが用いられ
ており、これ以下の軟化点のインクを用いると紙の非1
TIII像部分にirJれ(地肌汚れ)を生じたり、画
像流れを生じたりした。
これらの欠点を改良士る他の方法として、支持nニー+
ユに順次、離望層、インク層を設け、いわゆる284晴
成にしてう7ペーパーへの印′7°品貿を高〜5よ)と
いう試みが提案されている6しかしながら、この試1ト
でC土インクRりが削〜IR4上りP7いため、う7ペ
ーパーへの印字に際し、転写洩れ、字欠は等が2 rp
−し、良質な印字が得られないという欠点があり、また
11’ N7紙に対する印字品質ら決して充分なもので
はない。In the thermal transfer recording method, it is known that the surface properties of the thermal transfer image receiving paper require a large color tube to be placed on the image6.
If the surface smoothness of the paper (paper) decreases, ink will not be able to enter the four parts, and the transfer rate will decrease (the image will stick). To improve this drawback, it is effective to increase the fluidity of heat-softening inks (make them easier to flow) when heated, but such inks need to have their softening point lowered to some extent. Ta. Currently, ink with a softening point of 60 to 80°C is used, and if ink with a softening point below this is used, it will cause the paper to deteriorate.
irJ blur (background stain) or image blurring occurred in the TIII image area. Another way to improve these shortcomings is to use support n knee +
It has been proposed that a release layer and an ink layer be sequentially applied to the paper, so that the so-called 284 Seisei paper can be printed on another paper with a high to 5 degree.6 However, this first trial Because the C soil ink R is scraped ~ IR4 up P7, there are transfer leaks, missing characters, etc. when printing on U7 paper.
However, it has the disadvantage that good quality printing cannot be obtained, and the printing quality on 11'N7 paper is by no means sufficient.
本発明の目的は、粗い表面を有する紙は勿論、平滑な紙
にも高濃度かつ高品質で印字ができ、地汚れがなく、シ
かもブロックキング耐性に優れた感熱転写記録媒体を提
供することにある。An object of the present invention is to provide a thermal transfer recording medium that can print with high density and quality not only on paper with a rough surface but also on smooth paper, is free from scumming, and has excellent resistance to scratches and blocking. It is in.
【発明のも1戊】
本発明の目的は、支持体上に組成の異なる複数の層を有
する感熱転写記録媒体において、前記組成の異なる複数
の屑のうち少なくとも1.Illの隣接する2Mについ
て、支持体に遠い屑の厚みの、支持体に近い層の厚みに
対する比率を0.3〜1.0にし、かつ支持体に遠い層
に着色剤を含有せしめることにより達成された。
すなわち、厚みの比率が0.3〜1.0である本発明の
感熱転写記録媒体で印字すると、ラフペーパーに対して
エツジ部が欠けることなくシャープな印字ができ、更に
平滑紙に印字した場合にも印字すべき部分のみが転写さ
れた。この様に2層の厚みの比率が0.3〜1.0であ
る場合には、どの様な紙質の場合にも良好な印字ができ
た。
:れに対し、厚みの比率が0.3より小さいとラフペー
パーに対する印字のシャープネス底下や字欠けが発生し
、また、比率が1.0を越えると平滑紙に対して非印字
部の転写が発生し、共に良質な印字が得られない。
以下、本発明をより具体的に説明する。
本発明ににいて隣接する2JV1のうち、支持体に近い
層は熱)H触性物質を主成分としく以下、熱溶融性層と
称する)、支持体に遠い層は熱可塑性樹脂を主成分とす
る(以下、熱可塑性層と称する)ことが好ましい。
熱可塑性層に要求される機能は、記録パターンに応じて
、加熱されたところは可塑化して被転写紙の表面に粘着
し、加熱されないところは被転写紙に全く粘着を起こさ
ないものである。また、被転写紙に粘着を起こすところ
と起こさないところで綺麗にちぎれることが聚求される
。
熱溶融性層の機能は、上記の記録パターンに応じて、加
熱されたところは熱溶融して熱可塑性層が被転写紙層に
粘着するのを助け、加熱されないところは熱可塑性層と
の接着力によって熱可塑性7Mが被転写紙に容易に転写
しないようにするものである。
本発明者らは、熱可塑性層の厚みと熱溶融性層の厚みの
比率が0.3〜1.0にすることによって、上記熱可塑
性層、熱溶融性層の機能が充分に発揮され、う7紙から
平滑紙まで広範囲の紙質に良好な転写パターンが得られ
ることを見い出した。
本発明に用いられる熱溶融性物質としては、常温では固
体あるいは半固体の物質が挙げられ、融点(柳本MPJ
−2型による測定値)又は軟化点(環球法による測定値
)が25〜120 ’Cのものが好ましく、より好まし
くは40・〜120℃の固体の物質である。几本例とし
ては、例えばカルナバワックス、木ロウ、オウリキュリ
ーロウ、エスパルトロウ等の植物ロウ、蜜ロウ、昆虫ロ
ウ、セラックロウ、鯨ロウ等の動物口ン、パラフィンワ
ックス、マイクロクリスタリンワックス、エステル7ノ
クス、酸化ワックス等の石油aつ、モンタンロウ、オシ
ケライト、セレシン等の鉱物ロウ等のワックス類の他に
;パル tン酸、ステアリン酸、マルがリン酸、べへン
酸等の高級脂肪酸;パルミチルアルコール、ステアリル
アルコール、ベヘニルアルコール、マル〃ニルアルコー
ル、ミリシルアルコール、エイコサ/−ル等の高級アル
コール:パルミチン酸セチル、パルミチン酸ミリシル、
ステアリン酸セチル、ステアリン酸ミリシル等の高級脂
肪酸エステル;アセトアミン、プロピオン酸アミド、パ
ルミチン酸アミド、ステアリン酸アミド、アミドワック
ス等のアミド類;エテルガム、ロジマレイン酸樹脂、ロ
ノン7工/−ル84 m 、水添ロジン等のロジン誘導
体;7エ/−ル系樹脂、テルペン系樹脂、キシレン系樹
脂、低分子量スチレン樹脂、石油i?S樹脂、芳香族系
炭化水素系樹脂、エチレン−酢酸ビニル共重合体、エチ
レン−アクリル酸エチル共重会体、スチレン−ブタノエ
ン共重合体、スチレン−エチレン−ブチレン共重合体、
アイオノマー系樹脂、ポリアミド系樹脂、ポリエステル
系樹脂、エポキシ系樹脂、ポリウレタン系樹脂、アクリ
ル系樹脂、塩化ビニル系0I脂、セルロース系樹脂、ボ
リビニルアルコールM 4J(脂、スチレン系樹脂、イ
ンプレンゴム、クロロプレンゴム、天然ゴム等の品分p
物;ステアリルアミン、ベヘニルアミン、バルミチルア
ミン等の高級アミン類等が挙げられ、また特開昭54−
68253号に記載されている[常温で固体の熱可融性
固体状成分]や、特開昭55−105579号に記載さ
れている[ビヒクル]を用いてもよい。
これら熱溶融性物質は容易に水系ディスバージ1ンにす
ることができ好適に用いられる。
これらの熱溶融性物質は中、独もしくは2種以上混合し
て用いることができる。
熱溶融性物質を水系ディスパーツ9ンとするには、乳剤
削を含む系で転相法、高圧乳化法など既知の方法で水中
に乳化させればよい。乳化剤としては7ニオン性、アニ
オン性、カチオン性、両性のいずれでもよい。
本発明において熱溶融性層を形成する成分の組成比は限
定されないが、熱溶融性層の固形分総量100重量部に
対し、熱溶融性物質は10重量部以上(より好ましくは
30重量部以上)の使用が好ましい。
また、熱溶融性層に必要に応じてXf色材を添加しても
よい。着色材の使用機は熱溶融性層の固形分総Fit1
00重鼠部に灯して20重量部以下で・あることが好、
ましい。
本発明の熱)8触性層には上記成分の池、熱可塑性樹脂
、あるいは各種の添加剤が含有せしめられてもよい。例
えば、ひまし油、亜麻仁油、オリーブ油の如き植物油、
鯨油の如き動物油および鉱油が好適に使用されてよい。
また、7ニオン性界面活性剤、カチオン性界面活性剤、
ノニオン性界面活性剤、両性界面活性剤の如き界面活性
剤も好適に使用される。
本発明の熱溶融性層は10μ2以−ヒ、より好ましくは
0.5〜8μlとされればよい。
本発明で用いられる熱可塑性樹脂としては、エステル〃
ム、ロジンマレイン酸樹脂、ロノンフェノール用脂、水
添ロジン等のロジン誘導体、フェノール系4jI11t
、テルペン系樹脂、キシレン系樹脂、石油系樹脂、芳香
族系炭化水素樹脂、アイオノマー樹脂、ポリエステル系
樹脂、ポリアミド系樹脂、ポリエチレン・ポリプロピレ
ンi樹脂等があり、これらは既知の方法により容易に水
系分散物にすることがでさる。
より好ましい樹脂としてアクリル系樹脂が挙げられる。
アクリル系樹脂は、アクリル酸、メタクリル酸等の一塩
基性カルボン酸あるいはそのエステルと、少なくとも1
種の共重合し得るモノマーとの乳化重合によって得られ
る。カルボン酸モノマーとしては、アクリル酸あるいは
メタクリル酸のメチル、エチル、イソプロピル、ブチル
、イソブチル、アミル、ヘキシル、オクチル、2−エチ
ルヘキシル、デシル、ドデシル、ヒドロキシエチル、ヒ
トミキシプロピルエステル等が挙げられる。また共重合
し得るモノマーとしては、酢酸ビニル、塩化ビニル、塩
化ビニリデン、無水マレイン酸、無水7マル酸、スチレ
ン、2−メチルスチレン、クロルスチレン、アクリロニ
トリル、ビニルトルエン、N−メチロールアクリルアミ
ド、N−メチロールメタクリルアミド、N−ブトキシメ
チルアクリルアミド、トブトキシメタクリルアミド、ビ
ニルピリジン、N−ビニルピロリドン等が挙げられ、こ
れらの・1種あるいは2種以」二より選ばれる。
またツエン系共重合体も好ましく、ブタジェン、イソプ
レン、インブチレン、クロロプレン等のツエン系モノマ
ーと上記共重合し得るモノマーとの乳化重合物、例えば
ブタンエン−スチレン、ブタジェン−スチレン−ビニル
ピリノン、ブタノエン−7クリロニトリル、クロロプレ
ン−スチレン、クロロプレン−アクリロニトリル等があ
る。
また、より好ましい樹脂としてエチレン共重合体があり
、例えばエチレン−酢酸ビニル、エチレン−アクリル酸
エチル、エチレン−7タクリル酸メチル、エチレン−ア
クリル酸イソブチル、エチレン−アクリル酸、エチレン
−ビニルアルコール、エチレン−塩化ビニル、エチレン
−アクリル酸金属塩等の共重合体を挙げることがでさる
。
その池、熱可塑性樹脂としてポリウレタン系重合体、ポ
リエステル系重合体などもある。
熱可塑性樹脂の水系ディスパージョンは、熱溶融性物質
の水系ディスパージョンをyt造する方法と同様の方法
を用いることかて゛き、通常の7L比重ひ法によって得
ることもできる。
本発明において熱可塑性層を形成する成分の組成比は限
定されないが、熱可塑性層の固形分総量100重量部に
対し、着色剤は5〜40重ia部(より好ましくは5〜
35重量部)、熱可塑性物質は5〜95重量部(より好
ましくは10〜90重″i8.部)の使用が好ましい。
本発明の熱可塑性層には上記成分の他、各種の添加剤が
含有せしめられてもよい。例えば、ひまし油、亜麻仁油
、オリーブ油の如き植物油、鯨油の如き動物油および鉱
油が好適に使用されてよい。また、アニオン性、カチオ
ン性、ノニオン性、両性界面活性剤も好適に使用される
。また前記の熱溶融性物質も好適に用いられる。
本発明の可塑性層に用いる着色剤はカーボンプラ7りの
池に無代顔料、有様顔料または有機染料の任意の6のを
加えてよい。無代顔料の例としては、二酸化チタン、酸
化亜鉛、プルシアンブルー、硫化>トミウム、酸化鉄な
らびに鉛、亜鉛、バリウム及びカルシウムのクロム酸塩
などがある。有機顔料としては、アゾ、チオインノボ、
アントヂキノン、アントアンスロン、トリ7エンノオキ
サ/ン系ノ顔料、バット染料顔料、7タロシアニン顔料
、例えば;1!7りロシアニン及びその誘導体ならびに
キナクリドン顔料などがある。
有(茂染料としては、酸化染料、直接染料、分散染料、
油溶性染料、含金属油溶性染料などが挙げられる。
本発明の感熱転写記録媒体に用いられる支持体は、耐熱
強度を有し、寸法安定性および表面平滑性の高い支持体
が望ましい。材料としては、例えば、許通紙、コンデン
サー紙、ラミネート紙、コート紙等の紙類、あるいはポ
リエチレン、ポリエチレンテレフタレート、ポリスチレ
ン、ポリプロピレン、ポリイミド等の樹脂フィルム類お
よび紙−樹脂フイルム曳訃体、アルミ箔等の金属シート
等がいずれら好適に使用される。支持体の厚さは良好な
熱伝導性をうる上で通常約60μs以下、特に1.5〜
15μlであるのが好ましい。なおまた、本発明の感熱
転写記録媒体は、その支持体裏面側の構成は任意であり
、スティッキング防止層等のバ/キング層を設けてもよ
い。
本発明の感熱転写記録媒体において、熱溶融性層及び熱
可塑性層を含む構成R1を重合体フィルム等の支持体に
塗布するのに適した技術は、当業界にオ;いて公知であ
り、これらの公知技術は本発明にも適用できる。例えば
熱溶融性層及び熱可塑性層を含む構成層はその水系分散
物組成物(ラテックス)を水系コーティングして形成せ
しめた層である。本発明の熱溶融性Rη及び熱可塑性層
を含む構成層の塗布方法としては、リバースロールコー
タ−法、押出コーター法、グラビアコーター法やワイヤ
ーバー塗布法等、汗、法の技術を採用できる。本発明の
熱可塑性層は10μl以下、より好ましくは0.5〜5
μIとされればよい。
本発明の感熱転写記録媒体は、下塗WI(例えば膜付き
調整のための層。)、オーバーコート層等の池の構成層
を有してもよい。
本発明の感熱転写記録媒体を用いて熱忙写記tiする方
法について以下に述べる。
本発明の感熱転写記録媒体の構成層面と汀通紙の如き記
録シートとを重ねて、画像の情報に応じテサーマルへラ
ドやサーマルベン或いはレーサーを用いる熱記録装置に
よって感熱転写記録媒体11111から及び/又は記録
シート側からエネルギーをり。
えると、熱可塑性層は比較的低いエネルギーを5−えら
れることによって、着色剤等が熱可塑性物質と共に記録
シートに転写される。An object of the present invention is to provide a thermal transfer recording medium having a plurality of layers having different compositions on a support, in which at least one of the plurality of scraps having different compositions is removed. For the adjacent 2M of Ill, this is achieved by setting the ratio of the thickness of the waste far from the support to the thickness of the layer close to the support to be 0.3 to 1.0, and by containing a colorant in the layer far from the support. It was done. That is, when printing with the thermal transfer recording medium of the present invention having a thickness ratio of 0.3 to 1.0, sharp printing can be performed on rough paper without chipping of the edges, and furthermore, when printing on smooth paper, Only the part that should be printed was transferred. In this way, when the ratio of the thicknesses of the two layers was 0.3 to 1.0, good printing was possible on any paper quality. : On the other hand, if the thickness ratio is less than 0.3, the sharpness of the print on rough paper will be poor or the characters will be missing, and if the ratio exceeds 1.0, the transfer of non-printed areas will occur on smooth paper. In both cases, high-quality printing cannot be obtained. The present invention will be explained in more detail below. In the present invention, among the adjacent 2JV1, the layer closer to the support is mainly composed of a heat-sensitive substance (hereinafter referred to as a heat-fusible layer), and the layer far from the support is mainly composed of a thermoplastic resin. (hereinafter referred to as a thermoplastic layer) is preferable. The function required of the thermoplastic layer is to plasticize and stick to the surface of the transfer paper in areas that are heated, depending on the recording pattern, and to not cause any adhesion to the transfer paper in areas that are not heated. In addition, it is required that the transfer paper can be torn cleanly in areas where it will stick and where it will not. The function of the heat-fusible layer is to help the thermoplastic layer adhere to the transfer paper layer by melting the heat in the areas that are heated, and to help the thermoplastic layer adhere to the transfer paper layer in the areas that are not heated, depending on the recording pattern described above. This prevents the thermoplastic 7M from being easily transferred to the receiving paper due to force. The present inventors have found that by setting the ratio of the thickness of the thermoplastic layer to the thickness of the thermofusible layer to be 0.3 to 1.0, the functions of the thermoplastic layer and the thermofusible layer are fully exhibited, It has been found that good transfer patterns can be obtained on a wide range of paper qualities, from paper to smooth paper. The heat-melting substances used in the present invention include substances that are solid or semi-solid at room temperature, and whose melting point (Yanagimoto MPJ
It is preferably a solid substance with a softening point (measured by Type-2) or a softening point (measured by ring and ball method) of 25 to 120'C, more preferably 40 to 120C. Examples include plant waxes such as carnauba wax, wood wax, auriculie wax, and esparto wax; animal waxes such as beeswax, insect wax, shellac wax, spermaceti wax; paraffin wax, microcrystalline wax, and ester 7-nox. In addition to waxes such as petroleum waxes such as , oxidized wax, mineral waxes such as montan wax, osikerite, and ceresin; higher fatty acids such as palutonic acid, stearic acid, malphosphoric acid, and behenic acid; palmityl Higher alcohols such as alcohol, stearyl alcohol, behenyl alcohol, marnyl alcohol, myricyl alcohol, eicosa/ol: cetyl palmitate, myricyl palmitate,
Higher fatty acid esters such as cetyl stearate and myricyl stearate; amides such as acetamine, propionic acid amide, palmitic acid amide, stearic acid amide, and amide wax; ether gum, rhodimaleic acid resin, ronone 7/-84 m, water Rosin derivatives such as added rosin; 7-ether resin, terpene resin, xylene resin, low molecular weight styrene resin, petroleum i? S resin, aromatic hydrocarbon resin, ethylene-vinyl acetate copolymer, ethylene-ethyl acrylate copolymer, styrene-butanoene copolymer, styrene-ethylene-butylene copolymer,
Ionomer resin, polyamide resin, polyester resin, epoxy resin, polyurethane resin, acrylic resin, vinyl chloride 0I resin, cellulose resin, polyvinyl alcohol M4J (fat, styrene resin, imprene rubber, chloroprene) Items of rubber, natural rubber, etc.
compounds; higher amines such as stearylamine, behenylamine, and valmitylamine;
The [thermofusible solid component that is solid at room temperature] described in No. 68253 and the [vehicle] described in JP-A-55-105579 may also be used. These thermofusible substances can be easily converted into aqueous dispersion and are preferably used. These heat-melting substances can be used alone or in combination of two or more. In order to make a thermofusible substance into an aqueous dispersant, it may be emulsified in water by a known method such as a phase inversion method or a high pressure emulsification method in a system including emulsion removal. The emulsifier may be 7-ionic, anionic, cationic or amphoteric. In the present invention, the composition ratio of the components forming the heat-fusible layer is not limited; ) is preferred. Further, an Xf coloring material may be added to the heat-fusible layer as necessary. The machine used for coloring material is the total solid content of the heat-fusible layer Fit1
It is preferable that the amount is 20 parts by weight or less when compared to 00 parts by weight,
Delicious. The thermoplastic layer of the present invention may contain the above components, a thermoplastic resin, or various additives. For example, vegetable oils such as castor oil, linseed oil, olive oil,
Animal oils such as whale oil and mineral oils may be suitably used. In addition, 7-ionic surfactants, cationic surfactants,
Surfactants such as nonionic surfactants and amphoteric surfactants are also preferably used. The heat-fusible layer of the present invention may have a volume of 10 μl or more, more preferably 0.5 to 8 μl. As the thermoplastic resin used in the present invention, ester
Rosin derivatives such as rosin, maleic acid resin, rononphenol fat, hydrogenated rosin, phenolic 4jI11t
, terpene resins, xylene resins, petroleum resins, aromatic hydrocarbon resins, ionomer resins, polyester resins, polyamide resins, polyethylene/polypropylene resins, etc., and these can be easily dispersed in water by known methods. It is possible to make things into things. More preferred resins include acrylic resins. The acrylic resin contains at least one monobasic carboxylic acid such as acrylic acid or methacrylic acid or an ester thereof.
Obtained by emulsion polymerization of seeds with copolymerizable monomers. Examples of carboxylic acid monomers include methyl, ethyl, isopropyl, butyl, isobutyl, amyl, hexyl, octyl, 2-ethylhexyl, decyl, dodecyl, hydroxyethyl, and human mixypropyl esters of acrylic acid or methacrylic acid. In addition, monomers that can be copolymerized include vinyl acetate, vinyl chloride, vinylidene chloride, maleic anhydride, 7-maric anhydride, styrene, 2-methylstyrene, chlorostyrene, acrylonitrile, vinyltoluene, N-methylol acrylamide, N-methylol Examples include methacrylamide, N-butoxymethylacrylamide, tobutoxymethacrylamide, vinylpyridine, and N-vinylpyrrolidone, and one or more of these may be selected. Also preferred are tsene-based copolymers, such as emulsion polymers of tsene-based monomers such as butadiene, isoprene, imbutylene, and chloroprene and the above-mentioned copolymerizable monomers, such as butane-styrene, butane-styrene-vinylpyrinone, butanoene-7-pyrinone, etc. Examples include nitrile, chloroprene-styrene, and chloroprene-acrylonitrile. Further, more preferable resins include ethylene copolymers, such as ethylene-vinyl acetate, ethylene-ethyl acrylate, ethylene-methyl 7-tacrylate, ethylene-isobutyl acrylate, ethylene-acrylic acid, ethylene-vinyl alcohol, and ethylene-vinyl alcohol. Examples include copolymers of vinyl chloride and ethylene-acrylic acid metal salts. In addition, thermoplastic resins include polyurethane polymers and polyester polymers. The aqueous dispersion of a thermoplastic resin can be obtained by a method similar to that for producing an aqueous dispersion of a thermofusible substance, or by a conventional 7L specific gravity method. In the present invention, the composition ratio of the components forming the thermoplastic layer is not limited, but the colorant may be 5 to 40 parts by weight (more preferably 5 to 40 parts by weight) per 100 parts by weight of the total solid content of the thermoplastic layer.
35 parts by weight), and the thermoplastic substance is preferably used in an amount of 5 to 95 parts by weight (more preferably 10 to 90 parts by weight). In addition to the above components, the thermoplastic layer of the present invention contains various additives. For example, vegetable oils such as castor oil, linseed oil, and olive oil, animal oils such as whale oil, and mineral oils may be preferably used.Anionic, cationic, nonionic, and amphoteric surfactants are also suitable. The above-mentioned heat-melting substances are also suitably used.The coloring agent used in the plastic layer of the present invention is any one of six types of pigments, pigments, and organic dyes added to the carbon plastic layer. Examples of free pigments include titanium dioxide, zinc oxide, Prussian blue, tomium sulfide, iron oxides and chromates of lead, zinc, barium and calcium.Organic pigments include azo , thioinnovo,
Examples include anthodiquinone, anthurone, tri-7-ennooxan-based pigments, vat dye pigments, 7-thalocyanine pigments, such as; 1!7-lycyanine and derivatives thereof, and quinacridone pigments. Yes (Shige dyes include oxidation dyes, direct dyes, disperse dyes,
Examples include oil-soluble dyes and metal-containing oil-soluble dyes. The support used in the thermal transfer recording medium of the present invention preferably has heat-resistant strength, high dimensional stability, and high surface smoothness. Materials include, for example, paper such as transparent paper, capacitor paper, laminated paper, and coated paper, resin films such as polyethylene, polyethylene terephthalate, polystyrene, polypropylene, and polyimide, paper-resin film carriers, and aluminum foil. Metal sheets such as the above are preferably used. The thickness of the support is usually about 60 μs or less, especially 1.5 μs or less in order to obtain good thermal conductivity.
Preferably it is 15 μl. Furthermore, in the thermal transfer recording medium of the present invention, the structure on the back side of the support may be optional, and a backing layer such as an anti-sticking layer may be provided. In the thermal transfer recording medium of the present invention, techniques suitable for applying composition R1 comprising a heat-fusible layer and a thermoplastic layer to a support such as a polymeric film are well known in the art; The known techniques can also be applied to the present invention. For example, the constituent layers including the thermofusible layer and the thermoplastic layer are formed by aqueous coating of the aqueous dispersion composition (latex). As a coating method for the constituent layers including the heat-fusible Rη and the thermoplastic layer of the present invention, techniques such as a reverse roll coater method, an extrusion coater method, a gravure coater method, and a wire bar coating method can be employed. The thermoplastic layer of the present invention is 10 μl or less, more preferably 0.5 to 5 μl.
It suffices if it is μI. The thermal transfer recording medium of the present invention may have other constituent layers such as an undercoat WI (for example, a layer for adjusting film attachment) and an overcoat layer. A method for thermal printing using the thermal transfer recording medium of the present invention will be described below. The constituent layers of the thermal transfer recording medium of the present invention are stacked with a recording sheet such as paper, and the thermal transfer recording medium 11111 and/or Or apply energy from the recording sheet side. In other words, the thermoplastic layer is subjected to relatively low energy, so that the coloring agent and the like are transferred to the recording sheet together with the thermoplastic material.
以下、実施例を挙げるが、本発明の実施態様がこれらに
限定されるものではない。なお、以下に用いる1部1と
は「重量部」を示す。
実施例1
:(,5μsP7のポリエチレンテレフタレートフィル
ム上に下記塗布組成物をワイヤーバーを用いて、表−1
に示Vように乾燥膜〃を変化させた熱溶融性層を形成し
た。
バラ74 ン7−/りX (M!、!、’、’+70℃
)水性分散1(固形分30%)95部
エチレン−酢酸ビニル共重合体ラテックス(酢酸ビニル
含量25f6 固形分40%)4部
界面活性剤(弗素系2e!6水溶液) 2部これら
熱溶融性層の上に、下記の熱可塑性層塗布、111成物
をワイヤーバーで塗布、乾燥し感熱転写記12 K1.
l−ド試料を得た。ただし、乾燥膜厚は表−1に示す
ように、それぞれ変化させた。
2−エチルへキシルアクリレート−メチル、/タフリレ
ート−スチレン共重合体ラテックス(固形分54タロ)
19部カーボンブランク水分
故物(固形分32%)10部
界面活性剤(弗素系2%水溶液) 3部人−1
実施例2
3.5μI/7のポリエチレンテレフタレートフィルム
−1−に下記の塗布組成物をワイヤーバーを用いて、表
−2に示すように乾燥膜厚を変化させた熱溶融性Rりを
形成した。
カルナバワックス(融点80℃)水性分散物(固形分3
0%)80部
エチレン−酢酸ビニル共重合体ラテックス(酢酸ビニル
含量25% 固形分40%)16部界面活性剤(弗素系
2%水溶a) 2部熱溶融性層の」二に、下記
の塗布組成物をワイヤーバーで、それぞれ表−2に示す
※l燥膜厚となるよう熱可塑性層を塗布し、感熱転写記
録媒体試料を作成した。
2−エチルへキシルアクリレート−スチレン共重合体ラ
テックス(固形分42%)18部エチレン−酢酸ビニル
共重合体ラテックス(酢酸ビニルを量25%固形分40
%) 8部カーボンブラック水分故物(固形分3
2%)10部
界面活性剤(弗素系2%水溶液) 3部*′1
5
表−2
実施例1及び2で得られたkA熱転写記録媒体試料をサ
ーマルプリンター(発熱索子密度7doL/yyの薄膜
型シリアルヘッドを搭載した試作機)を用いて、印加工
ネルで−1.0論j/dotをりえてう7紙(ベック平
滑度4秒)と杼通紙(ベック平滑度100秒)に印字し
た。この結果を表−3に示す。
表−3
面平滑度の低い紙にも高い紙にも良好な印字を与える。Examples are given below, but the embodiments of the present invention are not limited thereto. In addition, 1 part 1 used below indicates "part by weight." Example 1: (Table 1)
A heat-fusible layer was formed by changing the dry film as shown in Figure V. Rose 74 N7-/RiX (M!,!,','+70℃
) Aqueous dispersion 1 (solid content 30%) 95 parts Ethylene-vinyl acetate copolymer latex (vinyl acetate content 25f6 solid content 40%) 4 parts Surfactant (fluorine-based 2e!6 aqueous solution) 2 parts These heat-fusible layers The following thermoplastic layer coating 111 composition was applied using a wire bar and dried to form a thermal transfer record 12 K1.
A l-do sample was obtained. However, the dry film thickness was varied as shown in Table 1. 2-ethylhexyl acrylate-methyl/tafrylate-styrene copolymer latex (solid content 54 taro)
19 parts carbon blank water waste (solid content 32%) 10 parts surfactant (2% fluorine-based aqueous solution) 3 parts Person-1 Example 2 The following coating composition was applied to a 3.5μI/7 polyethylene terephthalate film-1- Using a wire bar, a heat-melting R film with a dry film thickness varied as shown in Table 2 was formed. Carnauba wax (melting point 80°C) aqueous dispersion (solid content 3
0%) 80 parts Ethylene-vinyl acetate copolymer latex (vinyl acetate content 25% solids content 40%) 16 parts surfactant (fluorine-based 2% water-soluble a) 2 parts heat-fusible layer A thermoplastic layer was coated with the coating composition using a wire bar so as to have a dry film thickness of *1 shown in Table 2 to prepare a thermal transfer recording medium sample. 2-ethylhexyl acrylate-styrene copolymer latex (solid content 42%) 18 parts ethylene-vinyl acetate copolymer latex (vinyl acetate amount 25% solid content 40)
%) 8 parts carbon black water waste (solid content 3
2%) 10 parts Surfactant (fluorine-based 2% aqueous solution) 3 parts*'1
5 Table-2 The kA thermal transfer recording medium samples obtained in Examples 1 and 2 were printed using a thermal printer (prototype machine equipped with a thin-film serial head with a heating cord density of 7 doL/yy) and printed with a printing panel of -1. 0 theory j/dot was printed on paper (Beck smoothness: 4 seconds) and shuttle paper (Beck smoothness: 100 seconds). The results are shown in Table-3. Table 3 Provides good printing on paper with both low and high surface smoothness.
Claims (1)
媒体において、前記組成の異なる複数の層のうち少なく
とも1組の隣接する2層について、支持体に遠い層の厚
みの、支持体に近い層の厚みに対する比率が0.3〜1
.0であり、かつ支持体に遠い層が着色剤を含有するこ
とを特徴とする感熱転写記録媒体。In a thermal transfer recording medium having a plurality of layers having different compositions on a support, for at least one set of adjacent two layers among the plurality of layers having different compositions, the thickness of the layer farthest from the support is closer to the support. Ratio to layer thickness is 0.3-1
.. 0, and a layer far from the support contains a colorant.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61025069A JPS62183384A (en) | 1986-02-07 | 1986-02-07 | Thermal transfer recording medium |
US06/913,323 US4818591A (en) | 1985-10-07 | 1986-09-30 | Thermal transfer recording medium |
DE19863634049 DE3634049A1 (en) | 1985-10-07 | 1986-10-07 | HEAT TRANSFER RECORDING MEDIUM |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61025069A JPS62183384A (en) | 1986-02-07 | 1986-02-07 | Thermal transfer recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62183384A true JPS62183384A (en) | 1987-08-11 |
Family
ID=12155635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61025069A Pending JPS62183384A (en) | 1985-10-07 | 1986-02-07 | Thermal transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62183384A (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59224392A (en) * | 1983-06-04 | 1984-12-17 | Canon Inc | Thermal transfer material |
JPS60189487A (en) * | 1984-03-08 | 1985-09-26 | Seiko Epson Corp | Ink sheet |
JPS61206693A (en) * | 1985-03-12 | 1986-09-12 | General Kk | Thermal transfer recording medium |
JPS62181188A (en) * | 1986-02-06 | 1987-08-08 | Canon Inc | Thermal transfer recording method and heat-generating member for use in said method |
JPS62181185A (en) * | 1986-02-06 | 1987-08-08 | Canon Inc | Thermal transfer material and thermal transfer recording method |
-
1986
- 1986-02-07 JP JP61025069A patent/JPS62183384A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59224392A (en) * | 1983-06-04 | 1984-12-17 | Canon Inc | Thermal transfer material |
JPS60189487A (en) * | 1984-03-08 | 1985-09-26 | Seiko Epson Corp | Ink sheet |
JPS61206693A (en) * | 1985-03-12 | 1986-09-12 | General Kk | Thermal transfer recording medium |
JPS62181188A (en) * | 1986-02-06 | 1987-08-08 | Canon Inc | Thermal transfer recording method and heat-generating member for use in said method |
JPS62181185A (en) * | 1986-02-06 | 1987-08-08 | Canon Inc | Thermal transfer material and thermal transfer recording method |
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