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JPH0453197B2 - - Google Patents
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JPH0453197B2 - - Google Patents

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Publication number
JPH0453197B2
JPH0453197B2 JP61033767A JP3376786A JPH0453197B2 JP H0453197 B2 JPH0453197 B2 JP H0453197B2 JP 61033767 A JP61033767 A JP 61033767A JP 3376786 A JP3376786 A JP 3376786A JP H0453197 B2 JPH0453197 B2 JP H0453197B2
Authority
JP
Japan
Prior art keywords
film
transfer
less
ribbon
ink 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.)
Expired - Lifetime
Application number
JP61033767A
Other languages
Japanese (ja)
Other versions
JPS62193889A (en
Inventor
Tomio Katayama
Yukihisa Sato
Hideo Kato
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Teijin Ltd
Original Assignee
Teijin Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Teijin Ltd filed Critical Teijin Ltd
Priority to JP61033767A priority Critical patent/JPS62193889A/en
Publication of JPS62193889A publication Critical patent/JPS62193889A/en
Publication of JPH0453197B2 publication Critical patent/JPH0453197B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/40Thermography ; 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
    • B41M5/41Base layers supports or substrates

Landscapes

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

Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 本発明はプリンター用転写リボンに関し、更に
詳しくは走行性、耐久性、転写性に優れたプリン
ター用転写リボンに関する。 従来技術 プリンター用転写リボンの基体には、ポリエス
テルフイルムが耐薬品性、強度、弾性率、耐熱
性、結晶性、高融点等の優れた性質を有する点か
ら広く用いられている。 しかし、従来の二軸配向ポリエステルフイルム
を用いたインク転写リボンでは、例えばドツトイ
ンパクト方式による転写時における印字部の打た
れ残りによるフイルムの変形や伸びが生じたり、
更にはポリエステル基体に塗布したインク層がリ
ボンの反対面(走行面)に転写してリボンの走行
面を汚し、これが走行系のガイドポスト等の接触
部に徐々にインクを蓄積させ、リボンの走行を阻
害し、極端な場合にはリボンが動かなくなる等の
トラブルが生じ、この改善が必要であつた。 発明の目的 本発明の目的は、上述の問題を解消し、走行
性、耐久性、転写性に優れたプリンター用転写リ
ボンを提供することにある。 発明の構成・効果 本発明の目的は、本発明によれば、厚さ1〜
25μmの二軸配向ポリエステルフイルムの片面に
転写インク層を設けたプリンター用転写リボンで
あつて、該フイルムは縦方向のヤング率が450〜
800Kg/mm2で、かつ縦方向及び横方向の150℃での
熱収縮率が7%以下であり、更に該フイルムの転
写インク層を設ける表面は三次元粗さ計で測定し
た突起数(Y:ケ/mm2)と突起高さ(X:μm)
との関係を表わす突起分布曲線がlog10Y>1.3の
領域において下記式(1) log10Y=−1.8×+3.9 ……(1) で表わされる線と交差せず、更に該突起分布の最
大値及び該最大値を超えた部分の曲線が下記式(2) log10Y≧−3.6×+2.8 ……(2) を満足する範囲にある表面特性を有することを特
徴とするプリンター用転写リボンによつて達成さ
れる。 本発明におけるポリエステルとは芳香族ジカル
ボン酸を主たる酸成分とし、脂肪族グリコールを
主たるグリコール成分とするポリエステルであ
る。かかるポリエステルは実質的に線状であり、
そしてフイルム形成性特に溶融成形によるフイル
ム形成性を有する。芳香族ジカルボン酸とは、例
えばテレフタル酸、ナフタレンジカルボン酸、イ
ソフタル酸、ジフエノキシエタンジカルボン酸、
ジフエニルジカルボン酸、ジフエニルエーテルジ
カルボン酸、ジフエニルスルホンジカルボン酸、
ジフエニルケトンジカルボン酸、アンスラセンジ
カルボン酸等である。脂肪族グリコールとは、例
えばエチレングリコール、トリメチレングリコー
ル、テトラメチレングリコール、ペンタメチレン
グリコール、ヘキサメチレングリコール、デカメ
チレングリコールの如き炭素数2〜10のポリメチ
レングリコールあるいはシクロヘキサンジメタノ
ールの如き脂環族ジオール等である。 本発明において、ポリエステルとしては例えば
アルキレンテレフタレート及び/又はアルキレン
ナフタレートを主たる構成成分とするものが好ま
しく用いられる。かかるポリエステルのうちでも
例えばポリエチレンテレフタレート、ポリエチレ
ン−2.6−ナフタレートはもちろんのこと、例え
ば全ジカルボン酸成分の80モル%以上がテレフタ
ル酸及び/又は2.6−ナフタレンジカルボン酸で
あり、全グリコール成分の80モル%以上がエチレ
ングリコールである共重合体が特に好ましい。そ
の際全酸成分の20モル%以下のジカルボン酸は上
記芳香族ジカルボン酸であることができ、また例
えばアジピン酸、セバチン酸の如き脂肪族ジカル
ボン酸;シクロヘキサン−1,4−ジカルボン酸
の如き脂環族ジカルボン酸等であることができ
る。また、全グリコール成分の20モル%以下は、
エチレングリコール以外の上記グリコールである
ことができ、あるいは例えばハイドロキノン、レ
ゾルシノール、2,2−ビス(4−ヒドロキシフ
エニル)プロパンの如き芳香族ジオール;1,4
−ジヒドロキシメチルベンゼンの如き芳香族を含
む脂肪族ジオール;ポリエチレングリコール、ポ
リプロピレングリコール、ポリテトラメチレング
リコールノ如きポリアルキレングリコール(ポリ
オキシアルキレングリコール)等であることもで
きる。 また、本発明で用いられるポリエステルには、
例えばヒドロキシ安息香酸の如き芳香族オキシ
酸;ω−ヒドロキシカプロン酸の如き脂肪族オキ
シ酸等のオキシカルボン酸に由来する成分を、ジ
カルボン酸成分およびオキシカルボン酸成分の総
量に対し20モル%以下で含有するものも包含され
る。さらに本発明におけるポリエステルには実質
的に線状である範囲の量、例えば全酸成分に対し
2モル%以下の量で、3官能以上のポリカルボン
酸又はポリヒドロキシ化合物、例えばトリメリツ
ト酸、ペンタエリスリトールを共重合したものを
包含される。 上記ポリエステルは、それ自体公知であり、且
つそれ自体公知の方法で製造することができる。 上記ポリエステルとしては、ο−クロロフエノ
ール中の溶液として35℃で測定して求めた固有粘
度が約0.4〜約0.9のものが好ましい。 また、上述のポリエステルは必要に応じて、安
定剤、着色剤、酸化防止剤等の添加剤を含有する
ものであつてもよい。 本発明における二軸配向ポリエステルフイルム
は、上述のポリエステルから製造される二軸配向
フイルムであり、かつ該フイルムは縦方向のヤン
グ率450〜800Kg/mm2、好ましくは500〜750Kg/
mm2、更に好ましくは520〜700Kg/mm2の特性を有す
るものである。なお、フイルムの縦方向はインキ
転写リボンの長手方向と一致する。この縦方向の
ヤング率が450Kg/mm2未満であると、フイルムが
伸びやすく、弾性回復しにくいため、転写リボン
として用いて印字すると、印字部は印字圧力によ
る塑性変形が生じ、必要以上に太く印字される等
印字の鮮明性が悪く、又該変形のため転写リボン
の巻取りの取扱い性が劣る等で好ましくない。ま
た、縦方向のヤング率が800Kg/mm2を越えると、
剛性が強いため、印字の圧力のためにフイルムが
裂けやすくなり、好ましくない。 更に、上記二軸配向フイルムは熱収縮率(無荷
重の状態で150℃の熱風中に30分間曝した時の変
形率)が縦方向及び横方向とも7%以下である必
要があり、好ましくはともに4%以下、更に好ま
しくはともに2%以下である。 フイルムの熱収縮率が7%を越えると、特に感
熱プリンター用の転写リボンに用いたときにリボ
ンの変形が激しく、印字の鮮明性が劣るとともに
該変形のため転写リボンの巻取り取扱い性が劣る
ようになり、またドツトインパクト方式において
も熱収縮率が7%を越える程のものは、印字部の
変形が生じやすくなり、好ましくない。 又、本発明におけるポリエステルフイルムの厚
さは1〜25μmが汎用的であり、好ましくは2〜
10μm、更に好ましくは3〜8μmである。フイル
ムの厚さが上述の範囲よりも薄いと強度が不足し
て、転写リボンとしたときの適正に欠け、更には
加工適性の面からも劣つたものとなり、一方上述
の範囲よりも厚いと、特に感熱転写方式では熱伝
達に時間がかかり記録速度を速めてしかも鮮明な
転写画質を得るには適さなくなるので好ましくな
い。 本発明における二軸配向ポリエステルフイルム
は、上述の縦方向ヤング率、熱収縮率及び厚さを
満足すると同時に、転写インク層を設ける表面が
三次元粗さ計で測定した突起数(Y:ケ/mm2)と
突起高さ(X:μm)との関係を表わす突起分布
曲線がlog10Y>1.3の領域において上記式(1)で表
わされる線と交差せず、更に該突起分布の最大値
及び該最大値を越えた部分の曲線が上記式(2)を満
足する範囲にある表面特性を有する必要がある。
フイルム表面粗さが式log10=−3.6×+2.8で表わ
される直線を下まわるか或いは最大値を越えた部
分で交差する(特に突起高さが大きい部分が交差
して下側に下る如き)突起分布を呈する場合に
は、インク層を塗工した後にロールに巻いたとき
フイルムの反対面(走行面)に該インクが転写し
やすくなり、リボンの走行面を汚し、これがリボ
ンの走行系のガイドポスト等の接触部に徐々にイ
ンクを蓄積させ、リボンの走行を阻害し、極端な
場合にはリボンが動かなくなる等のトラブルを生
じ、その他、フイルムの滑り性が悪くなる結果、
加工時にフイルムにしわが入つたりするので、好
ましくない。また、フイルムの表面粗さが上記式
(1)と交差する突起分布を呈する程粗れている場合
には、印字の鮮明さが悪くなり、又サーマルヘツ
ドの摩耗の原因となり、実用上問題となるので好
ましくない。 上述のフイルム表面は、更に、多重干渉反射式
顕微鏡(Tl単色光)で測定した突起数(ケ/mm2
と突起高さ(h:μm)が 1.5≧h>1.0 ……10ケ/mm2以下 1.0≧h>0.75 ……1〜30ケ/mm2 0.75≧h>0.5 ……15〜120ケ/mm2 0.5≧h>0.25 ……80ケ/mm2以上 を満足することが好ましい。この表面特性を満足
することは、インク層のフイルム反対面への転写
を防止する点から、また印字の鮮明性の面から、
特に好ましい。 又、フイルム表面の最大突起高さは3μm以下、
更に1.5μm以下であることが好ましい。 本発明における二軸配向ポリエステルフイルム
は、更に、転写インク層を設けない側の表面の摩
擦係数が0.5以下、更には0.45以下、特に0.35〜
0.45であり、かつ該摩擦係数の連続50回往復走行
テスト後の値が初期値に比して150%未満、更に
は120%未満であることが好ましい。この表面は
走行面を形成するから、摩擦係数が大きすぎると
リボンの走行性が低下し、はなはだしいときはリ
ボン切れを起し、またインクの転写を引き起すよ
うになり、好ましくない。 本発明における二軸配向ポリエステルフイルム
の上述の表面粗さは、フイルム中に不活性無機、
有機微粒子等を添加することによつて形成するの
が好ましい。この不活性微粒子を用いる場合は、
平均粒径が0.01〜10μmの粒子を0.01〜5重量%、
更には平均粒径が0.03〜4μmの粒子を0.01〜1.5重
量%添加させるのが好ましい。この際、添加する
不活性無機、有機の微粒子は単成分でもよく、二
成分ないしはそれ以上を同時に用いてもよい。 上述の不活性微粒子としては、本発明において
は、好ましくは二酸化ケイ素(水和物、ケイ藻
土、ケイ砂、石英等を含む);アルミナ;
SiO2分を30重量%以上含有するケイ酸塩(例え
ば非晶質或は結晶質の粘土鉱物、アルミノシリケ
ート(焼成物や水和物を含む)、温石綿、ジルコ
ン、フライアツシユ等)、Mg,ZnZr及びTiの
酸化物;Ca,及びBaの硫酸塩;Li,Na,及
びCaのリン酸塩(1水素塩や2水素塩を含む);
Li,Na,及びKの安息香酸塩;Ca,Ba,
Zn,及びMnテレフタル酸塩;Mg,Ca,Ba,
Zn,Cd,Pb,Sr,Mn,Fe,Co及びNiのチタン
酸塩;Ba,及びPbのクロム酸塩;炭素(例
えばカーボンブラツク、グラフアイト等);ガ
ラス(例えばガラス粉、ガラスビーズ等)Ca,
及びMgの炭酸塩;ホタル石;及びZnSが例
示される。更に好ましくは、無水ケイ酸、含水ケ
イ酸、酸化アルミニウム、ケイ酸アルミニウム
(焼成物、水和物等を含む)、燐酸1リチウム、燐
酸3リチウム、燐酸ナトリウム、燐酸カルシウ
ム、硫酸バリウム、酸化チタン、安息香酸リチウ
ム、これらの化合物の複塩(水和物を含む)、ガ
ラス粉、粘土(カオリン、ベントナイト、白土等
を含む)、タルク、ケイ藻土、炭酸カルシウム等
が例示される。 これらの不活性微粒子を含有するポリエステル
は、通常ポリエステルを形成するための反応時、
例えばエステル交換法による場合のエステル交換
反応中あるいは重縮合反応中の任意の時期又は直
接重合法による場合の任意の時期に、不活性微粒
子(好ましくはグリコール中のスラリーとして)
を反応系中に添加することにより製造することが
できる。好ましくは、重縮合反応の初期例えば固
有粘度が約0.3に至るまでの間に、不活性微粒子
を反応系中に添加するのが好ましい。 本発明で用いる二軸配向ポリエステルフイルム
は、その製造法によつて特に制限を受けないが、
通常所定割合の微粒子を含有するポリエステルを
溶融し、スリツト状のダイからシート状に押出
し、キヤステイングドラムで冷却固化して未延伸
シートとなし、続いて該未延伸シートを二軸方向
に延伸して製品(フイルム)とする方法で製造さ
れる。その際、本発明の要件を好適に満足するに
は、先ず温浴中にて前記未延伸シートを加熱しな
がら一軸方向に延伸し、しかる後前記延伸方向と
直角の方向に熱風中で加熱延伸する方法が好まし
い。 温浴中での第一次延伸では、温浴は沸とう水で
延伸倍率は2.5倍〜6.0倍、更には3.5倍〜5.5倍と
するのが好ましく、また第二次延伸では熱風温度
は60〜120℃、更には75〜110℃とし、延伸倍率は
2.5倍〜4.0倍、更には2.8倍〜3.7倍とするのが好
ましい。更に得られる二軸延伸フイルムは好まし
くは150〜245℃、更には好ましくは170〜240℃の
範囲の温度で1〜200秒程度熱固定する。更に又、
必要に応じて熱固定後に1〜30%の弛緩熱処理を
施すことも寸法安定性を高めるために効果的であ
る。 かくして得られる二軸配向ポリエステルフイル
ムは、通常、表裏面とも同じ表面特性を呈する。
この場合、転写インク層を設ける面は表面でも裏
面でも良い。 本発明において転写インク層は、特に限定され
るものではなく、周知のものを用いることができ
る。すなわち、バインダー成分、着色成分などを
主成分とし、必要に応じて柔軟剤、可撓剤、分散
剤、平滑化剤などを適量添加して構成される。 上述の主成分について更に具体的に説明する
と、先ず、バインダー成分としては、カルナウバ
ワツクス、バラフインワツクスなど周知のワツク
ス類や低融点の各種高分子物質が用いられ、又、
着色剤としてはカーボンブラツクを主体とし、そ
の他各種の染料、あるいは有機、無機の顔料が用
いられる。場合によつては転写インクには昇華型
のものも含んでよい。 転写インク層の形成は、通常の方法、例えば溶
剤を添加した状態でグラビユア、リバース、スリ
ツトダイ方式などの溶液塗工方法、あるいはホツ
トメルト塗工などを用いて行うことができる。 その際、二軸配向ポリエステルフイルムは、必
要に応じてコロナ放電処理やバインダーの下びき
コートなどの前処理を行つてもよい。 本発明のプリンター用転写リボンは、二軸配向
ポリエステルフイルムが本来有している優れた諸
特性、すなわち高い耐薬品性、強度、弾性率、耐
熱性、高融点等に加えて、走行面にインクが転写
して汚れを生じ、ガイドポスト等の走行系にイン
クの汚れが蓄積してリボンが走行しなくなる等の
問題を解消し、インパクト用に用いれば印字によ
る打たれ残りなどの塑性変形も小さく、かつ転写
画質に優れたリボンである。 実施例 以下、実施例を掲げて本発明を更に説明する。
なお、本発明における種々の物性値および特性は
以下の如くして測定されたものであり、かつ定義
される。 (1) 突起分布測定法 小坂研究所製三次元粗さ計(SE−3CK)を用
いて、針径2μmR、針圧30mg、測定長1mm、サン
プリングピツチ2μm、カツトオフ0.25mm、縦方向
拡大倍率2万倍、横方向拡大倍率200倍、走査本
数150本の条件にて突起分布を測定し、突起高さ
(x軸)は基準レベルからの面積比率が70%にな
る点の突起高さ(zレベル)を0レベルとし、そ
の高さとの差を突起高さとして、それに対応する
突起数をy軸にプロツトした。 (2) ヤング率測定 フイルムを試料巾10mm、長さ15cmに切り、チヤ
ツク間100mmにして引張速度10mm/分、チヤート
速度500mm/分にインストロンタイプの万能引張
試験装置にて引張つた。得られた荷重−伸び曲線
の立上り部の接線よりヤング率を計算した。 (3) 表面突起数 フイルムの表面に400〜500Å乃至それ以下の厚
みにアルミニウムを均一に真空蒸着し、反対の非
蒸着面(フイルム面)にコロジオンを塗つて貼付
け、乾燥した。Tl単色光多重干渉反射式顕微鏡
(例えば、Carl Zeiss JENA社製)を用い100倍
の倍率でアルミニウム蒸着面の任意の100cm2を観
察した。顕微鏡視野中の突起物の突起高さに対応
して生じる干渉縞を持つ突起数を各々カウントし
た。 (4) 熱収縮率 20mm巾に切り出したフイルムサンプルに300mm
間長の位置に標点を印しておき、150℃に加熱さ
れた循環型熱風機に無荷重で吊して30分間保持
し、その後取出して放冷後標点間の長さを読みと
つて、原長との差の原長に対する割合を%で表示
した。 熱収縮率(%)=(原長)−(加熱後長さ)/(原長)×1
00 (5) インキ転写性 厚さ10μmのフイルムの片面に カーボンブラツク 15重量部 カルナウバワツクス 35〃 エステルワツクス 32〃 ポリテトラヒドロフラン 13〃 シリコンオイル 5〃 からなる転写インク組成物を層の厚さ18μmとな
るようにグラビユア方式で塗工して得られた転写
シート状物で、10mm巾×20cm長のフイルムサンプ
ルを覆い、直径5cmで1Kgの硬質クロム処理ロー
ルで20回繰返し押圧した後該サンプルの転写イン
ク層に接触した面を、エチルアルコールで湿らせ
た綿棒でなぞり、その綿棒へのインクの付着程度
(汚れ程度)を目視評価にて5段階で判定した。 <5段階判定> ◎……インクの付着は全く認められない ○……インクの付着は殆んど認められない △……インクの付着はいく分認められる ×……インクの付着はかなりの程度認められる ××……インクの付着がはげしく認められる (6) 走行性 図1に示した装置を用いて下記のように測定し
た。図1中、1はロードセル、2は表面粗さ約
0.5μmのプラスチツク製の固定棒(外径5mmφ)
3は荷重(100gr)、5,6はサンプル固定具、
4はサンプル(リボン)をそれぞれ示す。 温度20℃、湿度60%RHの環境で巾8mmのサン
プル(前記(4)に示した組成からなる転写インク層
を18μmの厚さに塗工した)の転写インクの塗工
面の反対面(走行面)を、2の固定棒に90°で接
触させて毎秒30mmの速さで1のロードセルを水平
に30cmの長さを往復移動させることにより摩擦係
数を読みとつた。 走行性の良否は、測定開始直後に得られる摩擦
係数に対する連続50回往復走行時の摩擦係数との
比較で3段階で判定した。 <3段階判定> ○…初期の摩擦係数に対する、50回繰返し往復走
行時の摩擦係数が120%未満であり、摩擦係数
が繰返し走行によりあまり増大しない。 △…初期の摩擦係数に対する、50回繰返し往復走
行時の摩擦係数が120%以上150%未満であり、
摩擦係数の増加が繰返し走行により若干認めら
れる。 ×…初期の摩擦係数に対する、50回繰返し往復走
行時の摩擦係数が150%以上であり、摩擦係数
の増加が繰返し走行により顕著に認められる。 (7) 印字鮮明性 前記(4)に示した組成からなる転写インク層を
18μmの厚さに塗工した転写リボンのインク塗工
面の反対側を電動式タイプライターIBM82Cを用
いて、アルフアベツトの「Q」の文字を通常のタ
イプライター用紙に打ち、印字された「Q」の鮮
明性、印字の太さ、濃淡を目視にて3段階で判定
した。 <3段階判定> ○…印字は太くならず、濃淡斑もなく、鮮明であ
る △…印字はやや太めになつているが、まず鮮明で
ある ×…印字はかなり太めになつており、かつ部分的
に濃淡の斑が見られ、鮮明さに欠ける (8) フイルム変形度 前記(6)に示した方法で同一ケ所を連続5回打つ
てフイルムの打ち跡を目視にて3段階で判定し
た。 <3段階判定> ○…打ち跡は殆んど認められない △…打ち跡はやや認められる ×…打ち跡ははつきり認められる 実施例 1 エチレングリコール(以下EGと略称する)90
重量部にカオリン(平均粒径1.2μm)10重量部を
添加した後、混合攪拌を行なつてスラリーを得
た。 次に、ジメチルテレフタレート100重量部と
EG70重量部を酢酸マンガン4水和物0.035重量部
を触媒として常法通りエステル交換をせしめた後
上記で得られたカオリン(濃度0.4重量%対ポリ
マー)を攪拌下添加した。続いてリン酸トリメチ
ル0.03重量部及び三酸化アンチモン0.03重量部を
添加した後高温真空下で常法通り重縮合反応を行
い、固有粘度0.620のポリエチレンテレフタレー
トペレツトを得た。 更にこのポリエチレンテレフタレート(以下
PETと略称)ペレツトを170℃、3時間乾燥後押
出機ホツパーに供給し、溶融温度280〜300℃で溶
融し、この溶融ポリマーを1mmのスリツト状ダイ
を通して表面仕上げ0.3S程度、表面温度20℃の回
転冷却ドラム上に成形押圧し、厚み約110μmの未
延伸フイルムを得た。 引き続き、この未延伸を図2に示した如く4本
の加熱ロール31,32,33及び34で予熱し
た後直ちに温水バス37でフイルムを加熱し、該
温水バスの中のロール35とロール36との間で
縦方向に3.6倍に一段延伸した。 更に続いて1段延伸フイルムを熱風中110℃の
温度で横方向に3.9倍に延伸し、次いで230℃で15
秒間熱処理を施して7.5μmの厚さの二軸配向フイ
ルムを得た。なお、この時の延伸速度は20m/分
であつた。 このフイルムのヤング率、150℃での熱収縮率、
表面粗さ突起分布曲線、最大突起高さ、及びイン
ク層を塗工して転写リボンとしたとき、のインク
転写性、走行性、印字鮮明性及びフイルム変形度
はいずれも良好レベルであり、総合評価も良好で
あつた。これらの結果を表−1に示す。 実施例 2 実施例1のうち、添加滑剤として炭酸カルシウ
ム(平均粒径1.5μm)を対ポリマー当り0.4重量%
添加させた他は同一条件にて実施し、7.5μmの二
軸配向フイルムを得た。 この二軸配向フイルムは表面突起分布曲線が実
施例1で得たフイルムよりも粗目になり、その結
果としてインク転写性及び走行性の点が更に良好
となり、総合評価も非常に良好であつた。これら
の結果を表−1に示す。 実施例 3 実施例2にうち延伸倍率を縦倍率4.2倍、横倍
率3.2倍とし、横延伸後の熱固定温度を235℃とし
た他は実施例2と同様にして厚さ7.2μmの二軸配
向フイルムを得た。 その結果は表−1に示す如くで、いずれの項目
とも非常に良好であつた。 実施例 4 実施例1のポリマーを用いた他は、実施例3と
同一延伸・熱固定条件で処理し、厚さ7.3μmの二
軸配向フイルムを得た。 その結果は表−1に示す如くでいずれの項目と
も良好であつた。 実施例 5 実施例2のうち熱固定温度を215℃とした他は
実施例2と同一条件で延伸・熱固定処理し、厚み
7.5μmの二軸配向フイルムを得た。 その結果は表−1に示す如くで、いずれの項目
とも良好であつた。 実施例 6 実施例1のうち添加滑剤として炭酸カルシウム
(平均粒径1.5μm)を0.45重量%とシリカ(平均粒
径0.6μm)を0.25重量%とを用い、縦方向には4.5
倍延伸し、引き続き横方向には3.6倍延伸する他
は実施例1と同様に行つて厚み7.2μmの二軸配向
フイルムを得た。 その結果は表−1に示す如くで、いずれの項目
も良好であつた。 実施例 7 実施例6のうち、シリカ(平均粒径2.0μm)を
0.1重量%とカオリン(平均粒径0.9μm)を0.4重
量%を用いた他は、実施例6と同様に行つて厚み
7.2μmの二軸配向フイルムを得た。 その結果は表−1に示す如くで、いずれの項目
も良好であつた。
INDUSTRIAL APPLICATION FIELD The present invention relates to a transfer ribbon for printers, and more particularly to a transfer ribbon for printers that has excellent running properties, durability, and transferability. Prior Art Polyester films are widely used as substrates for transfer ribbons for printers because they have excellent properties such as chemical resistance, strength, elastic modulus, heat resistance, crystallinity, and high melting point. However, with conventional ink transfer ribbons using biaxially oriented polyester films, the film may be deformed or elongated due to unprinted areas during transfer using the dot impact method, for example.
Furthermore, the ink layer applied to the polyester substrate is transferred to the opposite surface (running surface) of the ribbon, staining the running surface of the ribbon. In extreme cases, troubles such as the ribbon not moving occur occur, and an improvement is needed. OBJECTS OF THE INVENTION An object of the present invention is to solve the above-mentioned problems and provide a transfer ribbon for printers that has excellent runnability, durability, and transferability. Structure and Effects of the Invention According to the present invention, the object of the present invention is to
A transfer ribbon for printers, which has a transfer ink layer on one side of a 25 μm biaxially oriented polyester film, and the film has a Young's modulus in the longitudinal direction of 450 to 450.
800Kg/mm 2 and a heat shrinkage rate of 7% or less at 150℃ in the longitudinal and lateral directions, and the surface on which the transfer ink layer is provided has a protrusion count (Y) measured with a three-dimensional roughness meter. : Ke/mm 2 ) and protrusion height (X: μm)
In the area where log 10 Y>1.3, the protrusion distribution curve representing the relationship between A printer characterized in that the maximum value of This is accomplished by using a transfer ribbon. The polyester in the present invention is a polyester containing an aromatic dicarboxylic acid as a main acid component and an aliphatic glycol as a main glycol component. Such polyester is substantially linear;
It also has film-forming properties, particularly film-forming properties by melt molding. Aromatic dicarboxylic acids include, for example, terephthalic acid, naphthalene dicarboxylic acid, isophthalic acid, diphenoxyethane dicarboxylic acid,
diphenyl dicarboxylic acid, diphenyl ether dicarboxylic acid, diphenyl sulfone dicarboxylic acid,
These include diphenylketone dicarboxylic acid and anthracene dicarboxylic acid. Aliphatic glycols include, for example, polymethylene glycols having 2 to 10 carbon atoms such as ethylene glycol, trimethylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, and decamethylene glycol, or alicyclic diols such as cyclohexanedimethanol. etc. In the present invention, polyesters containing, for example, alkylene terephthalate and/or alkylene naphthalate as main constituents are preferably used. Among such polyesters, for example, not only polyethylene terephthalate and polyethylene-2.6-naphthalate, but also terephthalic acid and/or 2,6-naphthalene dicarboxylic acid account for 80 mol% or more of the total dicarboxylic acid component, and 80 mol% of the total glycol component. Particularly preferred are copolymers in which the above is ethylene glycol. In this case, the dicarboxylic acid accounting for up to 20 mol% of the total acid component can be the above-mentioned aromatic dicarboxylic acids, and also include, for example, aliphatic dicarboxylic acids such as adipic acid and sebacic acid; It can be a cyclic dicarboxylic acid or the like. In addition, less than 20 mol% of the total glycol component is
Can be the above glycols other than ethylene glycol, or aromatic diols such as hydroquinone, resorcinol, 2,2-bis(4-hydroxyphenyl)propane; 1,4
-Aliphatic diols containing aromatics such as dihydroxymethylbenzene; polyalkylene glycols (polyoxyalkylene glycols) such as polyethylene glycol, polypropylene glycol, and polytetramethylene glycol. In addition, the polyester used in the present invention includes
For example, components derived from oxycarboxylic acids such as aromatic oxyacids such as hydroxybenzoic acid; aliphatic oxyacids such as ω-hydroxycaproic acid are contained in an amount of 20 mol% or less based on the total amount of dicarboxylic acid components and oxycarboxylic acid components. It also includes those containing. Furthermore, the polyester in the present invention contains a trifunctional or more functional polycarboxylic acid or a polyhydroxy compound, such as trimellitic acid, pentaerythritol, in an amount within a substantially linear range, for example, an amount of 2 mol % or less based on the total acid components. Copolymerized products are included. The above polyester is known per se, and can be produced by a method known per se. The above-mentioned polyester preferably has an intrinsic viscosity of about 0.4 to about 0.9 measured as a solution in o-chlorophenol at 35°C. Moreover, the above-mentioned polyester may contain additives such as stabilizers, colorants, and antioxidants, as required. The biaxially oriented polyester film in the present invention is a biaxially oriented film manufactured from the above-mentioned polyester, and the film has a longitudinal Young's modulus of 450 to 800 Kg/mm 2 , preferably 500 to 750 Kg/mm 2 .
mm 2 , more preferably 520 to 700 Kg/mm 2 . Note that the longitudinal direction of the film coincides with the longitudinal direction of the ink transfer ribbon. If the Young's modulus in the longitudinal direction is less than 450 kg/mm 2 , the film tends to stretch and is difficult to recover elastically. Therefore, when used as a transfer ribbon for printing, the printed area will be plastically deformed due to printing pressure, making it thicker than necessary. This is undesirable because the clarity of the print is poor, and the deformation makes it difficult to handle when winding up the transfer ribbon. Also, if the Young's modulus in the longitudinal direction exceeds 800Kg/ mm2 ,
Due to the high rigidity, the film tends to tear due to the pressure of printing, which is undesirable. Furthermore, the biaxially oriented film must have a heat shrinkage rate (deformation rate when exposed to hot air at 150°C for 30 minutes under no load) of 7% or less in both the longitudinal and lateral directions, preferably Both are 4% or less, more preferably both are 2% or less. If the heat shrinkage rate of the film exceeds 7%, especially when used as a transfer ribbon for a thermal printer, the ribbon will be severely deformed, resulting in poor print clarity and poor handling when winding the transfer ribbon due to the deformation. Also, even in the dot impact method, if the thermal shrinkage rate exceeds 7%, the printed portion is likely to be deformed, which is undesirable. Further, the thickness of the polyester film in the present invention is generally 1 to 25 μm, preferably 2 to 25 μm.
It is 10 μm, more preferably 3 to 8 μm. If the thickness of the film is thinner than the above-mentioned range, the strength will be insufficient and it will not be suitable for use as a transfer ribbon, and will also be inferior in processing suitability.On the other hand, if the film is thicker than the above-mentioned range, In particular, the thermal transfer method is undesirable because it takes a long time to transfer heat, making it unsuitable for increasing the recording speed and obtaining clear transferred image quality. The biaxially oriented polyester film of the present invention satisfies the above-mentioned Young's modulus in the longitudinal direction, heat shrinkage rate, and thickness, and at the same time, the surface on which the transfer ink layer is provided has a protrusion count (Y: K/ mm 2 ) and the protrusion height (X: μm) does not intersect the line expressed by the above formula (1) in the area of log 10 Y > 1.3, and the maximum value of the protrusion distribution The curve in the portion exceeding the maximum value must have surface characteristics within a range that satisfies the above formula (2).
If the film surface roughness falls below the straight line expressed by the formula log 10 = -3.6 ) If the ribbon exhibits a protrusion distribution, when the ink layer is applied and then wound onto a roll, the ink is likely to be transferred to the opposite surface (running surface) of the film, staining the running surface of the ribbon, and causing damage to the ribbon running system. The ink gradually accumulates on the contact parts such as guide posts, which obstructs the running of the ribbon, causing problems such as the ribbon not moving in extreme cases, and other problems such as worsening the slipperiness of the film.
This is undesirable because it causes wrinkles in the film during processing. Also, the surface roughness of the film is expressed by the above formula.
If it is so rough that it exhibits a protrusion distribution that intersects (1), it is not preferable because the sharpness of the print becomes poor and it also causes wear of the thermal head, which poses a practical problem. The above-mentioned film surface also has a number of protrusions (k/mm 2 ) measured using a multiple interference reflection microscope (Tl monochromatic light).
and protrusion height (h:μm) is 1.5≧h>1.0 ...10 pieces/mm 2 or less 1.0≧h>0.75 ...1 to 30 pieces/mm 2 0.75≧h>0.5 ...15 to 120 pieces/mm 2 0.5≧h>0.25...It is preferable to satisfy 80 pieces/ mm2 or more. Satisfying this surface property is important from the viewpoint of preventing the transfer of the ink layer to the opposite side of the film and from the viewpoint of print clarity.
Particularly preferred. In addition, the maximum protrusion height on the film surface is 3μm or less,
Furthermore, it is preferably 1.5 μm or less. The biaxially oriented polyester film of the present invention further has a friction coefficient of 0.5 or less, further 0.45 or less, particularly 0.35 to 0.35 on the surface on which the transfer ink layer is not provided.
0.45, and the value of the friction coefficient after 50 consecutive reciprocating tests is preferably less than 150%, more preferably less than 120%, compared to the initial value. Since this surface forms a running surface, if the coefficient of friction is too large, the running properties of the ribbon will deteriorate, and if it is excessive, it will cause ribbon breakage and ink transfer, which is not preferable. The above-mentioned surface roughness of the biaxially oriented polyester film in the present invention is due to the presence of inert inorganic materials in the film.
It is preferable to form by adding organic fine particles or the like. When using this inert fine particle,
0.01 to 5% by weight of particles with an average particle size of 0.01 to 10 μm,
Furthermore, it is preferable to add particles having an average particle size of 0.03 to 4 μm in an amount of 0.01 to 1.5% by weight. At this time, the inert inorganic or organic fine particles added may be a single component, or two or more components may be used simultaneously. In the present invention, the above-mentioned inert fine particles are preferably silicon dioxide (including hydrates, diatomaceous earth, silica sand, quartz, etc.); alumina;
Silicates containing 30% by weight or more of SiO2 (e.g. amorphous or crystalline clay minerals, aluminosilicate (including calcined products and hydrated products), warm asbestos, zircon, fly ash, etc.), Mg, Oxides of ZnZr and Ti; Sulfates of Ca and Ba; Phosphates of Li, Na, and Ca (including monohydrogen salts and dihydrogen salts);
Benzoate of Li, Na, and K; Ca, Ba,
Zn, and Mn terephthalate; Mg, Ca, Ba,
Titanates of Zn, Cd, Pb, Sr, Mn, Fe, Co and Ni; Chromates of Ba and Pb; Carbon (e.g. carbon black, graphite, etc.); Glass (e.g. glass powder, glass beads, etc.) Ca,
and Mg carbonate; fluorite; and ZnS. More preferably, anhydrous silicic acid, hydrated silicic acid, aluminum oxide, aluminum silicate (including calcined products, hydrates, etc.), monolithium phosphate, trilithium phosphate, sodium phosphate, calcium phosphate, barium sulfate, titanium oxide, Examples include lithium benzoate, double salts of these compounds (including hydrates), glass powder, clay (including kaolin, bentonite, clay, etc.), talc, diatomaceous earth, calcium carbonate, and the like. Polyesters containing these inert particulates are usually reacted to form polyesters by
For example, inert fine particles (preferably as a slurry in glycol) may be used at any time during the transesterification reaction or polycondensation reaction when using the transesterification method, or at any time during the polycondensation reaction when using the direct polymerization method.
It can be produced by adding into the reaction system. Preferably, inert fine particles are added to the reaction system at the beginning of the polycondensation reaction, for example, until the intrinsic viscosity reaches about 0.3. The biaxially oriented polyester film used in the present invention is not particularly limited by its manufacturing method, but
Usually, polyester containing a predetermined proportion of fine particles is melted, extruded into a sheet through a slit die, cooled and solidified in a casting drum to form an unstretched sheet, and then the unstretched sheet is stretched biaxially. The product (film) is manufactured using the same method. At that time, in order to suitably satisfy the requirements of the present invention, the unstretched sheet is first stretched in a uniaxial direction while being heated in a warm bath, and then heated and stretched in a direction perpendicular to the stretching direction in hot air. The method is preferred. In the first stretching in a hot bath, the hot bath is boiling water and the stretching ratio is preferably 2.5 to 6.0 times, more preferably 3.5 to 5.5 times, and in the second stretching, the hot air temperature is 60 to 120 times. ℃, furthermore 75 to 110℃, and the stretching ratio is
It is preferably 2.5 times to 4.0 times, more preferably 2.8 times to 3.7 times. Further, the obtained biaxially stretched film is preferably heat set at a temperature in the range of 150 to 245°C, more preferably 170 to 240°C, for about 1 to 200 seconds. Furthermore,
If necessary, it is also effective to perform a relaxation heat treatment of 1 to 30% after heat setting to improve dimensional stability. The biaxially oriented polyester film thus obtained usually exhibits the same surface characteristics on both the front and back sides.
In this case, the surface on which the transfer ink layer is provided may be the front or back surface. In the present invention, the transfer ink layer is not particularly limited, and any known one can be used. That is, it is composed of a binder component, a coloring component, etc. as the main components, and an appropriate amount of a softener, a flexibilizing agent, a dispersant, a smoothing agent, etc. added as necessary. To explain the above-mentioned main components in more detail, first, as the binder component, well-known waxes such as carnauba wax and varafine wax, and various low-melting point polymer substances are used;
The coloring agent is mainly carbon black, and various other dyes or organic or inorganic pigments are used. In some cases, the transfer ink may also include a sublimation type. The transfer ink layer can be formed by a conventional method, for example, a solution coating method such as gravure, reverse, or slit die method in a state in which a solvent is added, or hot melt coating. At this time, the biaxially oriented polyester film may be subjected to pretreatment such as corona discharge treatment or subbing coating with a binder, if necessary. The transfer ribbon for printers of the present invention has the excellent properties originally possessed by biaxially oriented polyester films, such as high chemical resistance, strength, modulus of elasticity, heat resistance, and high melting point, as well as ink on the running surface. This eliminates problems such as ink stains being transferred and stains, and ink stains accumulating on the running system such as guide posts, which prevents the ribbon from running, and when used for impact printing, plastic deformation such as leftover marks due to printing is also small. , and is a ribbon with excellent transfer image quality. Examples Hereinafter, the present invention will be further explained with reference to Examples.
Note that various physical property values and characteristics in the present invention were measured and defined as follows. (1) Protrusion distribution measurement method Using a three-dimensional roughness meter (SE-3CK) manufactured by Kosaka Laboratory, needle diameter 2μmR, needle pressure 30mg, measurement length 1mm, sampling pitch 2μm, cutoff 0.25mm, vertical magnification 2 The protrusion distribution was measured under the conditions of 10,000 times, 200 times lateral magnification, and 150 scans, and the protrusion height (x axis) is the protrusion height (z) at the point where the area ratio from the reference level is 70%. Level) was set as 0 level, the difference from that height was set as the protrusion height, and the corresponding number of protrusions was plotted on the y-axis. (2) Young's Modulus Measurement The film was cut into sample widths of 10 mm and lengths of 15 cm, and stretched using an Instron type universal tensile tester at a chuck spacing of 100 mm at a tensile speed of 10 mm/min and a chatch speed of 500 mm/min. Young's modulus was calculated from the tangent to the rising portion of the obtained load-elongation curve. (3) Number of surface protrusions Aluminum was uniformly vacuum-deposited on the surface of the film to a thickness of 400 to 500 Å or less, and collodion was applied to the opposite non-vapor-deposited surface (film surface), followed by drying. An arbitrary 100 cm 2 of the aluminum vapor-deposited surface was observed at a magnification of 100 times using a Tl monochromatic light multiple interference reflection microscope (for example, manufactured by Carl Zeiss JENA). The number of protrusions with interference fringes generated corresponding to the protrusion height of the protrusions in the microscopic field of view was counted. (4) Heat shrinkage rate 300mm for a film sample cut out to a width of 20mm
Mark gauge marks at the distances between the gauges, hang them without a load in a circulating hot air fan heated to 150°C for 30 minutes, then take them out and leave them to cool, then read the length between the gauge marks. Then, the ratio of the difference from the original length to the original length is expressed as a percentage. Heat shrinkage rate (%) = (original length) - (length after heating) / (original length) x 1
00 (5) Ink transferability A transfer ink composition consisting of carbon black 15 parts by weight carnauba wax 35〃 ester wax 32〃 polytetrahydrofuran 13〃 silicone oil 5〃 is applied to one side of a 10 μm thick film in a layer thickness A film sample of 10 mm width x 20 cm length was covered with a transfer sheet obtained by coating with the gravure method to a thickness of 18 μm, and the sample was pressed 20 times with a 5 cm diameter hard chrome-treated roll weighing 1 kg. The surface in contact with the transfer ink layer was traced with a cotton swab moistened with ethyl alcohol, and the degree of ink adhesion to the cotton swab (staining degree) was visually evaluated on a five-point scale. <5-level evaluation> ◎...No ink adhesion is observed.○...Ink adhesion is almost not observed.△...Ink adhesion is somewhat observed.×...Ink adhesion is considerable. Recognized XX...Severe ink adhesion is observed (6) Running properties Measured as follows using the apparatus shown in Figure 1. In Figure 1, 1 is the load cell and 2 is the surface roughness.
0.5μm plastic fixing rod (outer diameter 5mmφ)
3 is the load (100gr), 5 and 6 are sample fixtures,
4 indicates a sample (ribbon). The surface opposite to the transfer ink coated surface (running The friction coefficient was read by making the load cell 1 contact the fixed rod 2 at 90° and moving the load cell 1 horizontally over a length of 30 cm at a speed of 30 mm per second. The running performance was judged on a three-level scale by comparing the friction coefficient obtained immediately after the start of measurement with the friction coefficient obtained during 50 consecutive reciprocating runs. <Three-stage judgment> ○...The friction coefficient after 50 repeated reciprocating runs is less than 120% of the initial friction coefficient, and the friction coefficient does not increase much due to repeated running. △…The friction coefficient when running back and forth repeatedly 50 times is 120% or more and less than 150% with respect to the initial friction coefficient,
A slight increase in the coefficient of friction is observed due to repeated running. ×...The friction coefficient after 50 repeated reciprocating runs is 150% or more with respect to the initial friction coefficient, and a significant increase in the friction coefficient is observed with repeated running. (7) Print clarity The transfer ink layer consisting of the composition shown in (4) above is
Using an electric typewriter IBM82C, type the letter "Q" in alpha alphabet on the opposite side of the ink-coated side of the transfer ribbon coated to a thickness of 18 μm onto regular typewriter paper. The clarity, print thickness, and shading were visually evaluated in three stages. <Three-level judgment> ○...Printing is not thick, there are no shading spots, and it is clear △...Printing is a little thick, but it is clear ×...Printing is quite thick, and there are some areas (8) Degree of film deformation The same spot was struck 5 times in a row using the method described in (6) above, and the marks on the film were visually judged on a three-grade scale. <Three-stage evaluation> ○...Almost no scratches are observed △...Some scratches are observed ×...Example: few scratches are observed Example 1 Ethylene glycol (hereinafter abbreviated as EG) 90
After adding 10 parts by weight of kaolin (average particle size 1.2 μm) to the parts by weight, mixing and stirring were performed to obtain a slurry. Next, 100 parts by weight of dimethyl terephthalate and
After transesterifying 70 parts by weight of EG in a conventional manner using 0.035 parts by weight of manganese acetate tetrahydrate as a catalyst, the kaolin obtained above (concentration 0.4% by weight to polymer) was added under stirring. Subsequently, 0.03 parts by weight of trimethyl phosphate and 0.03 parts by weight of antimony trioxide were added, and then a polycondensation reaction was carried out in a conventional manner under high temperature vacuum to obtain polyethylene terephthalate pellets having an intrinsic viscosity of 0.620. Furthermore, this polyethylene terephthalate (hereinafter
After drying the pellets (abbreviated as PET) at 170℃ for 3 hours, the pellets are fed to the extruder hopper and melted at a melting temperature of 280 to 300℃.The molten polymer is passed through a 1 mm slit die with a surface finish of about 0.3S and a surface temperature of 20℃. The film was molded and pressed onto a rotating cooling drum to obtain an unstretched film with a thickness of about 110 μm. Subsequently, as shown in FIG. 2, this unstretched film is preheated with four heating rolls 31, 32, 33, and 34, and immediately the film is heated in a hot water bath 37, and rolls 35 and 36 in the hot water bath are heated. The film was stretched 3.6 times in the longitudinal direction in one step. Subsequently, the first-stage stretched film was stretched 3.9 times in the transverse direction at a temperature of 110°C in hot air, and then stretched 15 times at a temperature of 230°C.
A biaxially oriented film with a thickness of 7.5 μm was obtained by heat treatment for seconds. Note that the stretching speed at this time was 20 m/min. Young's modulus of this film, heat shrinkage rate at 150℃,
The surface roughness protrusion distribution curve, maximum protrusion height, ink transferability, runnability, print clarity, and film deformation of the transfer ribbon after coating with the ink layer were all at a good level, and the overall The evaluation was also good. These results are shown in Table-1. Example 2 In Example 1, calcium carbonate (average particle size 1.5 μm) was added as an additive lubricant in an amount of 0.4% by weight based on the polymer.
A biaxially oriented film of 7.5 μm was obtained under the same conditions except for the addition. The surface projection distribution curve of this biaxially oriented film was rougher than that of the film obtained in Example 1, and as a result, the ink transferability and runnability were even better, and the overall evaluation was also very good. These results are shown in Table-1. Example 3 A biaxial film with a thickness of 7.2 μm was prepared in the same manner as in Example 2, except that the stretching ratio was 4.2 times in the longitudinal direction and 3.2 times in the lateral direction, and the heat setting temperature after the lateral stretching was 235° C. An oriented film was obtained. The results are shown in Table 1, and all items were very good. Example 4 A biaxially oriented film with a thickness of 7.3 μm was obtained by processing under the same stretching and heat setting conditions as in Example 3, except that the polymer of Example 1 was used. The results are shown in Table 1, and all items were good. Example 5 Stretching and heat setting were performed under the same conditions as in Example 2, except that the heat setting temperature was 215°C, and the thickness was
A biaxially oriented film of 7.5 μm was obtained. The results are shown in Table 1, and all items were good. Example 6 In Example 1, 0.45% by weight of calcium carbonate (average particle size 1.5 μm) and 0.25% by weight of silica (average particle size 0.6 μm) were used as additive lubricants, and 4.5% by weight of silica (average particle size 0.6 μm) was used in the longitudinal direction.
A biaxially oriented film with a thickness of 7.2 μm was obtained in the same manner as in Example 1, except that the film was stretched twice and then stretched 3.6 times in the transverse direction. The results are shown in Table 1, and all items were good. Example 7 Of Example 6, silica (average particle size 2.0 μm)
The thickness was
A biaxially oriented film of 7.2 μm was obtained. The results are shown in Table 1, and all items were good.

【表】【table】

【表】 * 総合評価 ◎…非常に良好、○…良好、△…やや
劣る、×…劣る
比較例 1 実施例1で得た未延伸フイルムを75℃にて予熱
し、更に低速、高速ロールの間で15mm上方より
900℃の表面温度の赤外線ヒーター1本にて加熱
し、該低速、高速ロールの表面速度差により3.3
倍に延伸し、続いてステンターに供給し、110℃
にて3.8倍に横方向に延伸した。得られた二軸延
伸フイルムを更に210℃にて15秒間熱固定して厚
み7.7μmのフイルムを得た。 得られた二軸配向フイルム及びインク層を塗工
してリボンとした後の各項目の評価結果は表−2
に示す如くであり、インク転写性及び走行性は一
応良好なレベルであつたが、フイルム変形度及び
印字鮮明性には劣り、総合評価としても劣るもの
であつた。 比較例 2 実施例2で得た未延伸フイルムを、比較例1の
延伸条件で二軸延伸し、その後温度215℃で熱固
定して厚み7.7μmの二軸配向フイルムを得た。 得られた二軸配向フイルム及びリボンの評価結
果は表−2に示す如くであり、比較例1に比して
インク転写性及び走行性は更に良好レベルにある
が、総合評価としては劣るものであつた。 比較例 3 添加滑剤としてカオリン(平均粒径0.5μm)を
対ポリマー0.5重量%添加して得た未延伸フイル
ムを、比較例1のうち縦の延伸倍率を3.6倍に延
伸し、熱固定温度を230℃にした他は比較例1と
同一の条件で延伸・熱固定して厚さ7.5μmの二軸
配向フイルムを得た。 得られた二軸配向フイルムの各項目は表−2に
示した如くであり、表面突起分布曲線が好適範囲
を下まわり、インク転写性、走行性とも劣り、総
合評価は悪いものであつた。 比較例 4 添加滑剤として炭酸カルシウム(平均粒径
1.5μm)を対ポリマー0.8重量%添加して得た未延
伸フイルムを、比較例1のうち縦の延伸倍率を
4.2倍、横の延伸倍率を3.5倍、熱固定温度を230
℃にした他は比較例1と同一の条件で処理して厚
さ7.5μmの二軸配向フイルムを得た。 得られた二軸配向フイルムの各項目の評価結果
は表−2に示した如くであり、表面突起分布曲数
が粗すぎて印字鮮明性は悪く、総合評価は劣つた
ものであつた。 比較例 5 添加滑剤として炭酸カルシウム(平均粒径
1.5μm)を対ポリマー0.4重量%添加させて得た厚
さ150μmの未延伸フイルムを、比較例1の条件の
うち、赤外線ヒーターとして表面温度750℃の赤
外線ヒーターを用い、低速、高速ロールの表面速
度比で縦方向に3.0倍に延伸し、次いで95℃の熱
風中で3.7倍の延伸倍率で横方向に延伸し、更に
再度縦方向に表面温度1000℃の赤外線ヒーターで
加熱して延伸倍率1.8倍で延伸し、その後220℃で
熱固定して厚さ7.5μmの二軸配向フイルムを得
た。 得られた二軸配向フイルムの各項目は表−2に
示す如くであり、プリンターで印字したとき印字
圧力でフイルムが縦方向に裂けてしまい、鮮明な
印字ができず総合評価は劣つたものであつた。 比較例 6 比較例2のうち熱固定温度を180℃にした他は
同一の条件で処理し厚さ7.5μmの二軸配向フイル
ムを得た。 得られた二軸配向フイルムの各項目は表−2に
示す如くであり、印字圧力によりフイルムの変形
がはげしく生じ、印字も太く、又、鮮明性の劣る
ものであり、総合評価は悪いものであつた。
[Table] * Overall evaluation ◎...Very good, ○...Good, △...Slightly poor, ×...Poor Comparative example 1 The unstretched film obtained in Example 1 was preheated at 75°C, and further rolled at low speed and high speed. From 15mm above between
Heated with one infrared heater with a surface temperature of 900℃, and due to the difference in surface speed between the low speed and high speed rolls
Stretched twice, then fed to a stenter and heated to 110℃
The film was stretched 3.8 times in the transverse direction. The obtained biaxially stretched film was further heat-set at 210° C. for 15 seconds to obtain a film with a thickness of 7.7 μm. The evaluation results for each item after coating the obtained biaxially oriented film and ink layer to form a ribbon are shown in Table 2.
As shown in Figure 2, the ink transferability and runnability were at a reasonably good level, but the degree of film deformation and print clarity were poor, and the overall evaluation was also poor. Comparative Example 2 The unstretched film obtained in Example 2 was biaxially stretched under the stretching conditions of Comparative Example 1, and then heat-set at a temperature of 215°C to obtain a biaxially oriented film with a thickness of 7.7 μm. The evaluation results of the obtained biaxially oriented film and ribbon are as shown in Table 2, and although the ink transferability and runnability are at a better level than Comparative Example 1, the overall evaluation is inferior. It was hot. Comparative Example 3 An unstretched film obtained by adding 0.5% by weight of kaolin (average particle size 0.5 μm) to the polymer as an additive lubricant was stretched to a longitudinal stretching ratio of 3.6 times that of Comparative Example 1, and the heat setting temperature was A biaxially oriented film with a thickness of 7.5 μm was obtained by stretching and heat setting under the same conditions as in Comparative Example 1 except that the temperature was 230°C. The properties of the obtained biaxially oriented film are as shown in Table 2, and the surface protrusion distribution curve was below the preferred range, the ink transferability and runnability were poor, and the overall evaluation was poor. Comparative Example 4 Calcium carbonate (average particle size
The unstretched film obtained by adding 0.8% by weight of 1.5 μm) to the polymer was
4.2 times, horizontal stretching ratio 3.5 times, heat setting temperature 230
A biaxially oriented film with a thickness of 7.5 μm was obtained by processing under the same conditions as in Comparative Example 1 except that the temperature was changed to ℃. The evaluation results for each item of the obtained biaxially oriented film are as shown in Table 2, and the number of curvatures in the distribution of surface protrusions was too rough, the printing clarity was poor, and the overall evaluation was poor. Comparative Example 5 Calcium carbonate (average particle size
An unstretched film with a thickness of 150 μm obtained by adding 0.4% by weight of 1.5 μm) to the polymer was heated under the conditions of Comparative Example 1, using an infrared heater with a surface temperature of 750°C, on the surface of low-speed and high-speed rolls. It was stretched at a speed ratio of 3.0 times in the longitudinal direction, then stretched in the transverse direction at a stretching ratio of 3.7 times in hot air at 95°C, and then heated again in the longitudinal direction with an infrared heater with a surface temperature of 1000°C to a stretching ratio of 1.8. The film was stretched at a double speed and then heat-set at 220°C to obtain a biaxially oriented film with a thickness of 7.5 μm. Each item of the obtained biaxially oriented film is as shown in Table 2. When printing with a printer, the film was torn in the vertical direction due to the printing pressure, making it impossible to print clearly, and the overall evaluation was poor. It was hot. Comparative Example 6 A biaxially oriented film with a thickness of 7.5 μm was obtained under the same conditions as in Comparative Example 2 except that the heat setting temperature was 180°C. The characteristics of the obtained biaxially oriented film are as shown in Table 2. The film was severely deformed due to the printing pressure, the printing was thick, and the clarity was poor, so the overall evaluation was poor. It was hot.

【表】 * 総合評価 ◎…非常に良好、○…良好、△…
やや劣る、×…劣る
[Table] * Overall evaluation ◎...Very good, ○...Good, △...
Slightly inferior, ×…inferior

【図面の簡単な説明】[Brief explanation of the drawing]

図−1は転写リボンの走行性の測定装置の模式
図である。図−2は本発明の実施例に用いた縦延
伸機の模式図である。図−3は三次元粗さ計で求
めたフイルム表面の突起高さ(Y:μm)と突起
の数(X:ケ/mm2)の関係を示す図である。
FIG. 1 is a schematic diagram of a device for measuring the runnability of a transfer ribbon. FIG. 2 is a schematic diagram of a longitudinal stretching machine used in an example of the present invention. FIG. 3 is a diagram showing the relationship between the height of protrusions on the film surface (Y: μm) and the number of protrusions (X: x/mm 2 ) determined by a three-dimensional roughness meter.

Claims (1)

【特許請求の範囲】 1 厚さ1〜25μmの二軸配向ポリエステルフイ
ルムの片面に転写インク層を設けたプリンター用
転写リボンであつて、該フイルムは縦方向のヤン
グ率が450〜800Kg/mm2で、かつ縦方向及び横方向
の150℃での熱収縮率が7%以下であり、更に該
フイルムの転写インク層を設ける表面は三次元粗
さ計で測定した突起数(Y:ケ/mm2)と突起高さ
(X:μm)との関係を表わす突起分布曲線が
log10Y>1.3の領域において下記式(1) log10Y=−1.8×+3.9 ……(1) で表わされる線と交差せず、更に該突起分布の最
大値及び該最大値を越えた部分の曲線が下記式(2) log10Y≧−3.6×+2.8 ……(2) を満足する範囲にある表面特性を有することを特
徴とするプリンター用転写リボン。 2 ポリエステルフイルムの転写インク層を設け
る表面が多重干渉反射式顕微鏡(Tl単色光)で
測定した突起数(ケ/mm2)と突起高さ(h:μm)
が 1.5≧h>1.0 ……10ケ/mm2以下 1.0≧h>0.75 ……1〜30ケ/mm2 0.75≧h>0.5 ……15〜120ケ/mm2 0.5≧h>0.25 ……80ケ/mm2以上 を満足することを特徴とする特許請求の範囲第1
項記載のプリンター用転写リボン。 3 ポリエステルフイルムの転写インク層を設け
ない側の表面は摩擦係数が0.5以下であり、かつ
該摩擦係数の連続50回往復走行テスト後の値が初
期値に比し150%未満であることを特徴とする特
許請求の範囲第1項又は第2項記載のプリンター
用転写リボン。
[Claims] 1. A transfer ribbon for printers, comprising a biaxially oriented polyester film with a thickness of 1 to 25 μm and a transfer ink layer provided on one side, the film having a Young's modulus in the longitudinal direction of 450 to 800 Kg/mm 2 and the heat shrinkage rate at 150°C in the longitudinal and lateral directions is 7% or less, and the surface on which the transfer ink layer of the film is provided has a protrusion count (Y: x/mm) measured with a three-dimensional roughness meter. 2 ) and the protrusion height (X: μm).
In the area of log 10 Y > 1.3, it does not intersect the line expressed by the following formula (1) log 10 Y = -1.8 A transfer ribbon for a printer, characterized in that the curve of the curved portion thereof has surface characteristics in a range that satisfies the following formula (2): log 10 Y≧−3.6×+2.8 (2). 2 The number of protrusions (ke/mm 2 ) and protrusion height (h: μm) measured using a multiple interference reflection microscope (Tl monochromatic light) on the surface of the polyester film on which the transfer ink layer is to be provided.
is 1.5≧h>1.0 …10 pcs/mm 2 or less 1.0≧h>0.75 …1 to 30 pcs/mm 2 0.75≧h>0.5 …15 to 120 pcs/mm 2 0.5≧h>0.25 ……80 Claim 1, which is characterized in that it satisfies not less than x/ mm2 .
Transfer ribbon for printers described in section. 3. The surface of the polyester film on which the transfer ink layer is not provided has a coefficient of friction of 0.5 or less, and the value of the coefficient of friction after 50 consecutive reciprocating tests is less than 150% of the initial value. A transfer ribbon for a printer according to claim 1 or 2.
JP61033767A 1986-02-20 1986-02-20 Transfer ribbon for printer Granted JPS62193889A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61033767A JPS62193889A (en) 1986-02-20 1986-02-20 Transfer ribbon for printer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61033767A JPS62193889A (en) 1986-02-20 1986-02-20 Transfer ribbon for printer

Publications (2)

Publication Number Publication Date
JPS62193889A JPS62193889A (en) 1987-08-26
JPH0453197B2 true JPH0453197B2 (en) 1992-08-25

Family

ID=12395594

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61033767A Granted JPS62193889A (en) 1986-02-20 1986-02-20 Transfer ribbon for printer

Country Status (1)

Country Link
JP (1) JPS62193889A (en)

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Publication number Priority date Publication date Assignee Title
JPH0218090A (en) * 1988-07-07 1990-01-22 Diafoil Co Ltd Thermal transfer polyphenylene sulfide film
JP2566624B2 (en) * 1988-07-14 1996-12-25 ダイアホイルヘキスト株式会社 Thermal transfer film
JPH0239998A (en) * 1988-07-29 1990-02-08 Diafoil Co Ltd Polyethylene naphthalate film for thermal transfer
JPH0247093A (en) * 1988-08-10 1990-02-16 Diafoil Co Ltd Transfer material for printer
JPH0247094A (en) * 1988-08-10 1990-02-16 Diafoil Co Ltd Transfer material for printer
JPH0248994A (en) * 1988-08-11 1990-02-19 Diafoil Co Ltd Thermal transfer material for printer
JP2911517B2 (en) * 1989-02-15 1999-06-23 大日本印刷株式会社 Thermal transfer sheet
US5250495A (en) * 1989-02-15 1993-10-05 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer recording process
JPH02219695A (en) * 1989-02-21 1990-09-03 Diafoil Co Ltd Polyester film for thermosensitive transfer
JP3010635B2 (en) * 1989-03-27 2000-02-21 三菱化学ポリエステルフィルム株式会社 Polyester film for thermal transfer
US6761968B2 (en) 2000-12-01 2004-07-13 Teijin Limited Biaxially oriented polyester film
JP6226245B2 (en) * 2015-09-24 2017-11-08 大日本印刷株式会社 Laminate of polyester resin composition
JP7583356B2 (en) * 2019-09-02 2024-11-14 東洋紡株式会社 Biaxially oriented polyester film

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JPS57160691A (en) * 1981-03-31 1982-10-04 Fujitsu Ltd Ink composition for heat transfer recording and heat transfer recording ink sheet employing said composition
JPS6025786A (en) * 1983-07-22 1985-02-08 Oji Paper Co Ltd Thermal transfer material
JPS60104392A (en) * 1983-11-10 1985-06-08 Konishiroku Photo Ind Co Ltd Thermal transfer recording medium
JPS60104393A (en) * 1983-11-11 1985-06-08 Konishiroku Photo Ind Co Ltd Thermal transfer recording medium
JPS60104395A (en) * 1983-11-11 1985-06-08 Konishiroku Photo Ind Co Ltd Thermal transfer recording medium
JPS60172587A (en) * 1984-02-17 1985-09-06 Victor Co Of Japan Ltd Thermal transfer recording ink sheet
JP2520389B2 (en) * 1984-02-20 1996-07-31 東レ株式会社 Thermal transfer material
JPS60217194A (en) * 1984-04-13 1985-10-30 Toray Ind Inc Transfer material for printer

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Publication number Publication date
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