JPS62193889A - Transfer ribbon for printer - Google Patents

Transfer ribbon for printer

Info

Publication number
JPS62193889A
JPS62193889A JP61033767A JP3376786A JPS62193889A JP S62193889 A JPS62193889 A JP S62193889A JP 61033767 A JP61033767 A JP 61033767A JP 3376786 A JP3376786 A JP 3376786A JP S62193889 A JPS62193889 A JP S62193889A
Authority
JP
Japan
Prior art keywords
film
transfer
ink layer
ribbon
biaxially oriented
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.)
Granted
Application number
JP61033767A
Other languages
Japanese (ja)
Other versions
JPH0453197B2 (en
Inventor
Tomio Katayama
片山 富夫
Yukihisa Sato
恭久 佐藤
Hideo Kato
秀雄 加藤
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)

Abstract

PURPOSE:To contrive higher feedability, durability and transfer properties, by specifying surface characteristics of a biaxially oriented polyester film of the titled ribbon which comprises a transfer ink layer on one side of the polyester film. CONSTITUTION:A transfer ink layer is provided on one side of a biaxially oriented polyester film. The film has a Young's modulus in the machine direction of 450-800kg/mm<2> and coefficients of heat shrinkage in the machine direction and the transverse direction at 150 deg.C of not more than 7%. The surface of the film on which the transfer layer is to be provided has such surface characteristics that a projection distribution curve representing the relationship between the number of projections (Y: pieces/mm<2>) and the projection height (X: mum) measured by a three-dimensional roughness tester does not intersect with a line represented by the Formula log10Y=-1.8X+3.9 in a region represented by log10Y>1.3, and the curve at the part of the maximum of the projection distribution and at the part beyond said part lies in a region represented by log10Y>=-3.6X+2.8. The polyester may be, for example, a polyester comprising an alkylene terephthalate and/or an alkylene naphthalate.

Description

【発明の詳細な説明】 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。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a transfer ribbon for a printer, and more particularly to a transfer ribbon for a printer that has excellent runnability, durability, and transferability.

従来技術 プリンター用転写リボンの基体には、ポリエステルフィ
ルムが斉;耐薬品性2強度2弾性率。
The base material of the transfer ribbon for conventional printers is a polyester film that has the same properties as chemical resistance, 2 strength, and 2 elastic modulus.

耐熱性、結晶性、高触点等の優れた性質を有する点から
広く用いられている。
It is widely used because it has excellent properties such as heat resistance, crystallinity, and high contact point.

しかし、従来の二軸配向ポリエステルフィルムを用いた
インク転写リボンでは、例えは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ィルム
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ボスト勢
の接触部に徐々にインクを蓄積させ、リボンの走行な1
511″#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った。
However, with conventional ink transfer ribbons using biaxially oriented polyester films, the film may be deformed or stretched due to unprinted areas during transfer using the dot impact method, and furthermore, the ink applied to the polyester substrate may The layer is transferred to the opposite side (running surface) of the ribbon, contaminating the running surface of the ribbon, and this gradually accumulates ink on the contact points of the guide posts in the running system, causing problems with the running of the ribbon.
511''#, and in extreme cases, problems such as the ribbon not moving occur, and this problem needs to be improved.

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。
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 running properties, durability, and transferability.

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I)エステルフィルムの片mIK転写インク
層を設けたプリンター用転写リボンであって、’Mフィ
ルムは縦方向のヤング率が450〜5oOky/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、更に該フィ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二ケ/j!I
I)と突起高さ(X:μm)との関係を表わす突起分布
曲線が1all、。y>1.3の領域において下記式(
1)%式%( で表わされる線と交差せず、更KMi突起分布の最大値
及び該最大値を越えた部分の曲線か下記式(2) %式%(2) を満足する範囲にある表面特性を有することな特徴とす
るプリンター用転写リボンによって達成される。
Structure/Effects of the Invention According to the present invention, there is provided a transfer ribbon for a printer provided with a biaxially oriented poly(I) ester film having a thickness of 1 to 25 μm. The film has a Young's modulus in the longitudinal direction of 450 to 5 oky/mm2
And the heat shrinkage rate at 150℃ in the vertical and horizontal directions is 7.
% or less, and furthermore, the surface of the film on which the transfer ink layer is provided has a protrusion count (Y2/j!I) measured with a three-dimensional roughness meter.
The protrusion distribution curve representing the relationship between I) and protrusion height (X: μm) is 1all. In the area of y>1.3, the following formula (
1) The maximum value of the KMi protrusion distribution and the curve of the part exceeding the maximum value, which does not intersect the line expressed by % formula % ( ), is within the range that satisfies the following formula (2) % formula % (2) This is achieved by a printer transfer ribbon characterized by having surface properties.

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、脂肪族グリコールな主たるグリコー
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、そしてフィルム形成性特に溶融
成形によるフィ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
、インフタル酸、ンフエノキンエタンジカルボン酸、ジ
フェニルジカルボン酸、ジフェニルニーデルジカルボン
酸、ジフェニルスルホンジカルボン酸、ジフェニルクト
ンジヵルボン酸、アンスラセンジカルボン酸等である。
The polyester in the present invention is a polyester having an aromatic dicarboxylic acid as the main acid component and an aliphatic glycol as the main glycol component. Such polyesters are substantially linear and have film forming properties, particularly by melt molding. Aromatic dicarboxylic acids include, for example, terephthalic acid, naphthalenedicarboxylic acid, inphthalic acid, nphenoquinethanedicarboxylic acid, diphenyldicarboxylic acid, diphenylneedledicarboxylic acid, diphenylsulfonedicarboxylic acid, diphenylctonedicarboxylic acid, anthracenedicarboxylic acid Acids etc.

脂肪族グリコールとは、例えばエチレングリコール、ト
リノチレングリコール、テトラメチレングリフール、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L2〜10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ツール
の如き脂環族ジオール等である。
Aliphatic glycols include, for example, ethylene glycol, trinotylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol,
These include polymethylene glycols having 2 to 10 carbon atoms such as decamethylene glycol, and alicyclic diols such as cyclohexane dimetatool.

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/又はフ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λ、乙− チーレフタル酸及び/又はす7タレンジカルポン酸であ
り、全グリフール成分の80モルチ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モルチ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7ジビン酸、セパチ
ン酸の如キ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モルチ以下
は、エチレングリフ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ルキノン、レゾルシノ
ール。
In the present invention, polyesters containing, for example, alkylene terephthalate and/or fullkylene naphthalate as main constituents are preferably used. Particularly preferred is a copolymer in which 80 moles or more of the total glyfur component is ethylene glycol, which is λ, thielephthalic acid and/or 7thalene dicarboxylic acid. In this case, the dicarboxylic acid of up to 20 molar of the total acid component can be the above-mentioned aromatic dicarboxylic acids, and also, for example, aliphatic dicarboxylic acids such as 7-divic acid and cepatic acid; cyclohexane-1,
It can be an alicyclic dicarboxylic acid such as 4-dicarboxylic acid. Also, up to 20 moles of the total glycol component can be the above-mentioned glycols other than ethylene glyfur, or for example hydroquinone, resorcinol.

2.2−ビス(4−ヒドロキシフェニル)プロパンの如
き芳香族ジオール;lI4−ジヒドロキンメチルベンゼ
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
レングリコールの如きポリフ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。
2. Aromatic diols such as 2-bis(4-hydroxyphenyl)propane; aliphatic diols containing aromatics such as lI4-dihydroquinemethylbenzene; polyfulkylene glycols such as polyethylene glycol, polypropylene glycol, polytetramethylene glycol ( Polyoxyalkylene glycol) and the like can also be used.

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
シカプー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モル条以下で含有するも
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モルチ以下の量で、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、例えばトリメリット酸、ペンタ
エリスリトールを共重合したものを包含される。
In addition, the polyester used in the present invention may contain a dicarboxylic acid component and a component derived from an oxycarboxylic acid such as an aromatic oxyacid such as hydroxybenzoic acid; an aliphatic oxyacid such as ω-hydroxycapunic acid; Those containing 20 moles or less based on the total amount of carboxylic acid components are also included. Furthermore, the polyester in the present invention contains a trifunctional or higher 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 mole or less based on the total acid component. Copolymerized products are included.

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。
The above polyester is known per se, and can be produced by a method known per se.

上記ポリエステルとしては、0−りL:lロブエノール
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。
The above-mentioned polyester has an intrinsic viscosity of about 0 as measured at 35°C as a solution in 0-L:l Robenol.
.. 4 to about 0.9 is preferred.

また、上述のポリエステルは必要に応じて、安定剤9着
色剤、酸化防止剤等の添加剤を含有するものであっても
よい。
Moreover, the above-mentioned polyester may contain additives such as a stabilizer 9, a coloring agent, and an antioxidant, if necessary.

本発明における二輪配向ポリエステルフィルムは、上述
のポリエステルから失透される二軸配向フィルムであり
、かつ該フィルムは縦方向のヤング率450〜5ooK
9./=、好ましくは500〜750 kq/ md、
更に好ましくは520〜700kg/−の特性を有する
ものである。なお、フィ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45
0に9/−未満であると、フィルムが伸びやすく、弾性
回復しKくいため、転与りポ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
The two-wheel oriented polyester film in the present invention is a biaxially oriented film devitrified from the above-mentioned polyester, and the film has a longitudinal Young's modulus of 450 to 5ooK.
9. /=, preferably 500-750 kq/md,
More preferably, it has a characteristic of 520 to 700 kg/-. Note that the longitudinal direction of the film coincides with the longitudinal direction of the ink transfer ribbon. This longitudinal Young's modulus is 45
If it is less than 0 to 9/-, the film tends to stretch and is difficult to recover elastically, so if it is used as a rolling pin to print, the printed area will be plastically deformed due to the printing pressure, resulting in thicker printing than necessary. This is not preferable because the clarity of printing is poor, and the deformation makes it difficult to handle when winding up the transfer ribbon.

また、縦方向のヤング率がsookg/−を越えると、
剛性が強いため、印字の圧力のためにフィルムが裂けや
すくなり、好ましくない。
Also, when the Young's modulus in the longitudinal direction exceeds sookg/-,
Due to the high rigidity, the film tends to tear due to the pressure of printing, which is undesirable.

更に、上記二軸配向フィルムは熱収縮率(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優以下である必要があり、好まし
くはともに4チ以下、更に好ましくはともに2%以下で
ある。
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 transverse directions, preferably Both are 4% or less, more preferably both are 2% or less.

フィルムの熱収縮率が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。
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.

又、本発明におけるポリエステルフィルムの厚さは1〜
25μmが汎用的であり、好ましくは2〜l OplN
 +更に好ましくは3〜8μmである。
Moreover, the thickness of the polyester film in the present invention is 1 to
25 μm is commonly used, preferably 2 to 1 OplN
+More preferably 3 to 8 μm.

フィ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性に欠け、更には加工適
性の面からも劣ったものとなり、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。
If the thickness of the film is thinner than the above-mentioned range, the strength will be insufficient, and it will lack suitability when used as a transfer ribbon, and will also be inferior in terms of 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.

本発明における二軸配向ポリエステルフィルムは、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針で測定し
た突起数(Y二ケ/mm2)と突起高さ(X:μm)と
の関係を表わす突起分布曲線が1oft、。Y)1.3
の領域において上記式(1)で表わされる線と)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。フィルム表面粗さが式logs。
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 three-dimensional roughness (number of protrusions measured with a three-dimensional roughness needle) (Y 2 / The protrusion distribution curve representing the relationship between the protrusion height (X: μm) and the protrusion height (mm2) is 1oft. Y) 1.3
has surface characteristics that do not intersect with the line expressed by the above formula (1) in the area of , and further the maximum value of the protrusion distribution and the curve of the portion exceeding the maximum value satisfy the above formula (2). There is a need. The film surface roughness is expressed as logs.

= −3,6X + 2.8で表わされる直線を下まわ
るか或は最大値を越えた部分で交差する(%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φ た後にfrp−ル巻いたときフィルムの反対面(走行面
)K該インクが転写しやす(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ボスト等の接触部に
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し、
その他、フィルムの滑り性が悪くなる結果、加工時1c
フイルムにしわが入ったりするので、好ましくない。ま
た、フィルムの表面粗さが上記式(gと交差する突起分
布を呈する根粗れている場合には、印字の鮮明さが悪く
なり、ヌサーマルヘッ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。
= -3,6 When the ink layer is coated and the film is rolled up, the ink is easily transferred to the opposite side (running surface) of the film and stains the running surface of the ribbon, which may damage the ribbon running system. The ink gradually accumulates on the contact parts such as guide posts, which obstructs the running of the ribbon and, in extreme cases, causes problems such as the ribbon not moving.
In addition, as a result of poor film slipperiness, 1c during processing
This is not desirable as it may cause wrinkles on the film. In addition, if the surface roughness of the film is rough with a protrusion distribution that intersects with the above formula (g), the sharpness of the print will deteriorate, causing wear of the thermal head, and causing practical problems. So I don't like it.

上述のフィルム表面は、更K、多重干渉反射式顕微m(
TJ単色光)で測定した突起数(ケ/mm2)と突起高
さ(h:μm)が 1.5≧h >  t、o     ・・・・・・  
 10ケ/mm2以下1.0≧h > 0.75   
 ・・・・・・1〜30ケ/mm20.75≧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。
The above-mentioned film surface was coated with a multi-interference reflection microscope (
The number of protrusions (ke/mm2) and the protrusion height (h: μm) measured with TJ monochromatic light are 1.5≧h > t, o...
10 pieces/mm2 or less 1.0≧h > 0.75
...1~30 pieces/mm20.75≧h>
0.5...15-120 pieces/mm2
0.5≦h > 0.25 ・・・・・・ 80 pieces/
It is preferable to satisfy mm2 or more.

この表面特性を満足することは、インク層のフィルム反
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1%に好ましい。
Satisfying this surface property is preferably 1% from the viewpoint of preventing transfer of the ink layer to the opposite side of the film and from the viewpoint of print clarity.

又、フィルム表面の最大突起高さは3μm以下、更K 
1.5μm以下であることが好ましい。
In addition, the maximum protrusion height on the film surface is 3 μm or less, and
It is preferable that it is 1.5 μm or less.

本発明における二軸配向ポリエステルフィルムは、更に
、転写インク層を設げない側の表面の摩擦係数が0.5
以下、更には0.45以下1%KO,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、
はなはだしいときにはリボン切れを起し、またインクの
転写を引き起すようKなり、好ましくない。
The biaxially oriented polyester film of the present invention further has a friction coefficient of 0.5 on the surface on which the transfer ink layer is not provided.
0.45 or less, 1% KO, 35 to 0.45, and the value of the friction coefficient after 50 consecutive reciprocating tests is less than 150%, further less than 120%, compared to the initial value. It is preferable that This surface forms the running surface, so if the coefficient of friction is too large, the running properties of the ribbon will decrease.
If it is too severe, it may cause ribbon breakage and ink transfer, which is undesirable.

本発明における二軸配向ポリエステルフィルムの上述の
表面粗さは、フィルム中に不活性無機、有機微粒子等を
添加することによっ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0.01−10p
m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。
The above-mentioned surface roughness of the biaxially oriented polyester film in the present invention is preferably achieved by adding inert inorganic or organic fine particles to the film. When using these inert fine particles, the average particle size is 0.01-10p.
m particles in an amount of 0.01 to 5% by weight, furthermore, the average particle size is 0.
Preferably, 0.01-1.5% by weight of particles of 0.03-4 μm are added. 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.

上述の不活性微粒子としては1本発明においては、好ま
しくは(1)二酸化ケイ素(水和物、ケイ凍土、ケイ砂
1石英等を含む);■アルミナ;■Sin、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、ンルフン、フライアッシュ等)、■Mg
+ZnZ「及びTiの酸化物;θJCa、及びBaの硫
酸塩;■Li、Na、及びCaのリン酸塩(l水素塩や
2水素塩を含む);■L i 、Na +及びKの安息
香酸塩;(’!J Ca + B a + Z n +
及びMnのテレフタル酸塩; (!、1Mg。
In the present invention, the above-mentioned inert fine particles preferably include (1) silicon dioxide (including hydrate, diatomaceous earth, silica sand, quartz, etc.); ■ alumina; ■ containing 30% by weight or more of Sin. silicates (e.g. amorphous or crystalline clay minerals, aluminosilicates (including calcined products and hydrated products), warm asbestos, asbestos, fly ash, etc.), ■Mg
+ ZnZ' and oxides of Ti; θJCa and sulfates of Ba; ■ phosphates of Li, Na, and Ca (including l-hydrogen salts and dihydrogen salts); ■ benzoic acid of Li, Na +, and K Salt; ('! J Ca + B a + Z n +
and Mn terephthalate; (!, 1 Mg.

Ca 、Ba +Zn 、Cd +Pb 、Sr 、M
n 、Fe 、Co及びNiのチタン酸塩;[相]Ba
、及びpb  のりρム酸塩;0炭素(例えばカーボン
ブラック、グラファイト等);0ガラス(例えばガラス
粉、ガラスピーズ等)◎Ca、及びMg  の炭酸塩;
■ホタル石;及び[相]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
lリチウム、燐酸3リチウム、燐酸ナトリウム。
Ca, Ba + Zn, Cd + Pb, Sr, M
titanate of n, Fe, Co and Ni; [phase] Ba
, and pb Normomate; 0 carbon (e.g. carbon black, graphite, etc.); 0 glass (e.g. glass powder, glass peas, etc.) ◎Ca and Mg carbonate;
(2) Fluorite; and [phase] ZnS are exemplified. More preferably, anhydrous silicic acid, hydrated silicic acid, aluminum oxide,
Aluminum silicate (including calcined products, hydrates, etc.), lithium phosphate, trilithium phosphate, sodium phosphate.

燐酸カルシウム、硫酸バリクム、酸化チタン。Calcium phosphate, baricum sulfate, titanium oxide.

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。
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.

これらの不活性微粒子を含有するポリエステルは1通常
ポリエステルを形成するための反応時1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K、不活性微粒子(好ましくはグリフール中のスラ
リーとして)を反応系中に添加することKより製造する
ことができろ。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K、不活性微粒子を反
応系中に添加するのが好ましい。
The polyester containing these inert fine particles can be prepared at any time during the reaction to form the polyester, such as 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. Phase K can be prepared by adding inert microparticles (preferably as a slurry in Glyfur) into the reaction system. Preferably, inert fine particles are added to the reaction system at the initial stage of the polycondensation reaction, for example, until the intrinsic viscosity reaches about 0.3.

本発明で用いる二軸配向ポリエステルフィルムは、その
製造法によっ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、スリット状の
ダイからシート状に押出し、キャスティングドラムで冷
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(フィルム)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
、先ず温浴中くて前記未延伸シートを加熱しなから一軸
方向に嶌伸し、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。
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-shaped die, and cooled and solidified in a casting drum. It is produced by a method in which an unstretched sheet is obtained, and then the unstretched sheet is biaxially stretched to produce a product (film). At that time, in order to suitably satisfy the requirements of the present invention, the unstretched sheet is first heated in a hot bath and stretched in a uniaxial direction, and then heated in hot air in a direction perpendicular to the stretching direction. A method of stretching is preferred.

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ィルムは好ましくは
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。
In the first stretching in a warm bath, the hot bath is boiling water and the stretching ratio is preferably 2.5 times to 6.0 times, more preferably 3.5 times to 5.5 times. For stretching, the hot air temperature is 60~
The temperature is 120°C, preferably 75 to 110°C, and the stretching ratio is 2.
It is preferably 5 times to 4.0 times, more preferably 2.8 times to 3.7 times. Furthermore, the biaxially stretched film obtained is preferably 150 to 245°C, more preferably 170 to 240°C.
Heat set at a temperature in the range of 1 to 200 seconds.

更に又、必要に応じて熱固定後Kl〜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
Furthermore, it is also effective to perform relaxation heat treatment at Kl ~ 30% after heat setting, if necessary, to improve dimensional stability.

かくして得られる二軸配向ポリエステルフィルムは、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真直でも良い。
The biaxially oriented polyester film thus obtained usually exhibits the same surface properties on both the front and back sides. In this case, the surface on which the transfer ink layer is provided may be a surface or a straight surface.

本発明において転写インク層は1%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2着包成分などを主成分とし、必要に応
じて柔軟剤、可撓剤1分散剤、平滑化剤などを適量添加
して構成される。
In the present invention, the transfer ink layer is not limited to 1%, and any known ink layer can be used. That is,
The main components are binder component 2, wrapping component, etc., and appropriate amounts of softener, flexibilizer 1, dispersant, smoothing agent, etc. are added as needed.

上述の主成分く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、カルナウバワックス、パラフ
ィンワックスなど周知のワッ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ッ
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。場合によっては転写インクには昇
華型のものも含んでよい。
To explain more specifically about the above-mentioned principal components, first,
As the binder component, well-known waxes such as carnauba wax and paraffin wax and various low-melting point polymer substances are used.As the coloring agent, carbon black is used as the main ingredient, and various other dyes and organic and inorganic dyes are used. Pigments are used. In some cases, the transfer ink may also include a sublimation type.

転写インク層の形成は、通常の方法、例えば溶剤を添加
した状態でグラピュア、リバース。
The transfer ink layer is formed using the usual methods, such as Grapure and Reverse with the addition of a solvent.

スリットダイ方式などの溶液塗工方法、あるいはホント
メルト塗工などを用いて行うことができる。
This can be carried out using a solution coating method such as a slit die method, or a true melt coating.

その際、二軸配向ポリエステルフィルムは、必要に応じ
てコpす放電処理やバインダーの下ひきコートなどの前
処理を行ってもよい。
At that time, the biaxially oriented polyester film may be subjected to pretreatment such as a coating discharge treatment or a subbing coat with a binder, if necessary.

本発明のプリンター用転写リボンは、二軸配向ポリエス
テルフィルムが本来有している優れた緒特性、すなわち
高い耐薬品性9強度1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産性変形も小さく、かつ転写
画質に優れたリボンである。
The transfer ribbon for printers of the present invention has excellent properties originally possessed by biaxially oriented polyester films, such as high chemical resistance, 9 strength, 1 elastic modulus, heat resistance, and high melting point. This eliminates problems such as ink stains accumulating on the running system such as guide posts and causing the ribbon to not run, and when used for impact printing, it also prevents productivity deformities such as unprinted marks due to printing. This ribbon is small and has excellent transfer image quality.

実施例 以下、実施例を掲げて本発明を更に説明する。Example The present invention will be further explained below with reference to Examples.

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。
Note that various physical property values and characteristics in the present invention were measured and defined as follows.

(1)突起分布測定法 小板研究所製三次元粗さ計(5E−3CK )を用いて
、針径2μmR、針圧30 M?+測定長1 tm 、
サンプリングピッチ2μm、カントオフ0,25 tl
 +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
さく x eAfi )は基準レベルからの面積比率が
70%になる点の突起高さく2レベル)をO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軸にプロットした。
(1) Protrusion distribution measurement method Using a three-dimensional roughness meter (5E-3CK) manufactured by Koita Institute, the needle diameter was 2 μmR and the needle pressure was 30 M? + measurement length 1 tm,
Sampling pitch 2μm, cantoff 0.25tl
+20,000x vertical magnification, 200x horizontal magnification,
The protrusion distribution was measured under the condition of 150 scans, and the protrusion height x eAfi) was defined as the O level at the point where the area ratio from the reference level was 70% (Protrusion height 2 level), and the difference from that height was calculated. is the protrusion height, and the corresponding number of protrusions is plotted on the y-axis.

チャック間100龍にして引張速度10朋/分。The chuck distance is 100 mm and the pulling speed is 10 mm/min.

チャート速度500n+/分にインストロツタイブの万
能引張試験装置にて引張った。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。
It was pulled in an Instrotsutive universal tensile tester at a chart speed of 500 n+/min. Young's modulus was calculated from the tangent to the rising portion of the obtained load-elongation curve.

(3)  表面突起数 フィルムの表面に400〜5ooX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(
フィルム面)にコージオンを塗って貼付け、乾燥した。
(3) Number of surface protrusions Aluminum is uniformly vacuum-deposited on the surface of the film to a thickness of 400 to 5ooX or less, and the opposite non-deposited surface (
Cordion was applied to the film surface), pasted, and dried.

Tl単色光多重干渉反射式顕微鏡(例えば、Carl 
Zetas 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100cIi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。
Tl monochromatic light multiple interference reflection microscope (e.g. Carl
An arbitrary 100 cIi of the aluminum vapor-deposited surface was observed at a magnification of 100 times using a micrometer (manufactured by Zetas 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)  熱収縮率 $ 20μm巾に切り出したフィルムサンプル300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って、原長との
差の原長に対する割合なチで表示した。
(4) Heat shrinkage rate: 300 film samples cut out to a width of 20 μm.Hanged without load on a heated circulating hot air blower for 30 minutes, then taken out and allowed to cool, then read the length between gauge marks. The difference from the original length is expressed as a percentage of the original length.

(5)  インキ転写性 厚さ10μmのフィルムの片面に カーボンブラック       15重量部カルナウバ
ワックス      35  gエステルワックス  
     32  〃ポリテトラヒドロンラン   1
3  〃シリコンオイル         51からな
る転写インク組成物を層の厚さ18μ電となるようにグ
ラピュア方式で塗工して得られた転写シート状物で、1
0I111I巾×20口長のフィルムサンプルを覆い、
直径5αでlkpの硬質クロム処理ロールで20回繰返
し押圧した後肢サンプルの転写インク層に接触した面を
、エチルアルフ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) Ink transferability Carbon black 15 parts by weight Carnauba wax 35 g Ester wax on one side of a 10 μm thick film
32 Polytetrahydrone 1
3. A transfer sheet-like material obtained by applying a transfer ink composition consisting of silicone oil 51 using the Grapure method to a layer thickness of 18 μm.
Cover a film sample of 0I111I width x 20 mouth length,
The surface of the hindlimb sample that was repeatedly pressed 20 times with a hard chromium-treated roll having a diameter of 5α and lkp was traced with a cotton swab moistened with ethyl alfur on the surface that was in contact with the transfer ink layer, and the degree of ink adhesion to the cotton swab (stain level) was measured. was visually evaluated on a five-point scale.

〈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公認められる×・・・・・・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IK示した装置を用いて下記のように測定した。図1
中、lはロードセル、2は表面粗さ約0.5μmのプラ
スチック製の固定棒(外径5Hφ)3は荷重(JOO&
r)+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。
<5-level evaluation> ◎...No ink adhesion is observed ○...
・・・・Almost no ink adhesion is observed △・・・・
・・Ink adhesion is recognized to a certain degree×・・・・Ink adhesion is recognized to a considerable extent××・・・・・・
Severe ink adhesion was observed (6) Runability Measurement was carried out as follows using the apparatus shown in Figure IK. Figure 1
In the middle, l is a load cell, 2 is a plastic fixed rod (outer diameter 5Hφ) with a surface roughness of about 0.5 μm, and 3 is a load (JOO&
r)+5+6 indicates a sample fixture, and 4 indicates a sample (ribbon).

温度20℃、湿度60%RHの環境で巾8龍のサンプル
(前記(4)に示した組成からなる転写インク層を18
μm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3
0關の2ikさでlのp−ドセルを水平に30口の長さ
を往復移動させることにより摩擦係数を読みとった。
A sample with a width of 8 dragons (a transfer ink layer having the composition shown in (4) above) was applied in an environment of a temperature of 20°C and a humidity of 60%
The surface opposite to the surface coated with the transfer ink (coated to a thickness of μm) (travel surface) is brought into contact with the fixing rod 2 at 90'', and the speed is 3 seconds.
The coefficient of friction was read by reciprocating the length of 30 mouths of a p-docel horizontally at a speed of 2 degrees.

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Nljr%係数との比較で
3段階で判定した。
The running performance was judged in three stages by comparing the friction coefficient obtained immediately after the start of measurement with the Nljr% coefficient obtained during 50 consecutive reciprocating runs.

〈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チ未満であり、摩擦係数が繰返
し走行によりあまり増大しt【い。
<Three-stage judgment> ○...The friction coefficient after 50 repeated reciprocating runs is less than 120 inches compared to the initial friction coefficient, and the friction coefficient does not increase much due to repeated running.

△・・・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12o%以上150チ未満であり、!
!!!擦係数の増加が繰返し走行により若干認められる
△...Relative to the initial friction coefficient. The friction coefficient when running back and forth 50 times is 12o% or more and less than 150%, and!
! ! ! A slight increase in the coefficient of friction is observed due to repeated running.

×・・・初期の摩擦係数に対する、50[il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。
x: The friction coefficient during repeated reciprocating running at 50[il] with respect to the initial friction coefficient is 150 or more, and a significant increase in the friction coefficient is observed with repeated running.

(7)  印字鮮明性 前記(4)K示した組成からなる転写インク層を18μ
m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−IBM82Cを用い−(、アル
ファベットのrQJの文字を通常のタイプライタ−用紙
に打ち、印字されたrQJ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 △・・・印字はやや太目になっているが、まず鮮明であ
る X・・・印字はかなり太目になっており、かつ部分的に
濃淡の斑が見られ、鮮明さに欠ける(8)  フィルム
変形度 前記(1J)に示した方法で同一ケ所を連続5回打って
フィルムの打ち跡を目視にて3段階で判定した。
(7) Print clarity The transfer ink layer consisting of the composition shown in (4)K above was coated with 18μ
Using an electric typewriter (IBM82C), type the letters rQJ on the opposite side of the ink-coated surface of the transfer ribbon coated to a thickness of m on regular typewriter paper. The quality, thickness, and shading of the print were visually judged in three stages. (Three-stage judgment) ○... The print is not thick, there are no shading spots, and it is clear. △... The print is slightly thick. However, first of all, it is clear. Using this method, the same spot was struck five times in a row, and the marks on the film were visually evaluated on a three-grade scale.

〈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 ×・・・打ち跡ははっきり認められる 実施例1 エチレングリフール(以下EGと略称する)90i量部
にカオリン(平均粒径1.2μm)10重量部を添加し
た後、混合攪拌を行なってスラリーを得た。
<Three-stage judgment> ○... Almost no scratches are observed △... Some scratches are visible ×... The scratches are clearly visible Example 1 Ethylene Glyfur (hereinafter abbreviated as EG) ) After adding 10 parts by weight of kaolin (average particle size 1.2 μm) to 90i parts, mixing and stirring were performed to obtain a slurry.

次に、ジメチルテレフクレー+・i o o重量部とE
G70重′jk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 i量チ対ポリマー
)を攪拌下添加した。
Next, add dimethyltereph clay+・i o o parts by weight and E
After transesterifying G70 parts by weight using 0.035 parts by weight of manganese acetate tetrahydrate as a catalyst in a conventional manner, the kaolin obtained above (concentration 0.4 parts per polymer) was added under stirring. did.

続いてリン酸トリメチル0.03重量部及び三酸化アン
チモア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ットを得た。
Subsequently, 0.03 parts by weight of trimethyl phosphate and 0.03 parts by weight of antimore 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.

更にこのポリエチレンテレフタレート(以下PETと略
称)ペレットを170℃、3時間乾燥後押出機ホッパー
に供給し、溶融温度280〜300℃で溶融し、この溶
融ポリマーをI Illのスリット状ダイを通して表面
仕上げ0.3S程度9表面温度20℃の回転冷却ドラム
上に成形押出し、厚み約110μmの未延伸フィルムを
得た。
After drying the polyethylene terephthalate (hereinafter abbreviated as PET) pellets at 170°C for 3 hours, the pellets are fed to an extruder hopper and melted at a melting temperature of 280 to 300°C. The product was formed and extruded on a rotating cooling drum with a surface temperature of 20° C. to obtain an unstretched film with a thickness of about 110 μm.

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でフィルムを加熱し、該温水バス中のロール3
5とロール36との温度で横力向1c 3.9倍に延伸
し、次いで230℃で15秒間熱処理を施して7.5μ
mの厚さの二軸配向フィルムを得た。なお、この時の延
伸速度は20 m 7分であった。
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.
5 and the roll 36 and stretched 3.9 times in the transverse force direction 1c, and then heat-treated at 230°C for 15 seconds to form a 7.5μ
A biaxially oriented film with a thickness of m was obtained. Note that the stretching speed at this time was 20 m and 7 minutes.

このフィルムのヤング率、150℃での熱収縮率1表面
粗さ突起分布曲線、最大突起高さ。
Young's modulus of this film, heat shrinkage rate at 150°C 1 surface roughness protrusion distribution curve, maximum protrusion height.

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評価も良好であっ
た。これらの結果を表−IK示す。
Also, when the ink layer was applied to form a transfer ribbon, the ink transferability, runnability, print clarity, and fill evaluation were also good. These results are shown in Table IK.

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f1%添
加させた他は同一条件にて実施し、7.5μmの二軸配
向フィルムを得た。
Example 2 The same conditions as in Example 1 were carried out except that calcium carbonate (average particle size 1.5 μm) was added as an additive lubricant at 0% and 4 times f1% per polymer, and a 7.5 μm biaxial An oriented film was obtained.

この二軸配向フィルムは表面突起分布曲線が実施例1で
得たフィ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
常に良好であった8これらの結果を表−1に示す。
The surface protrusion 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 good8. These results are shown in Table-1.

実施例3 実施例2のうち延伸倍率な縦倍率4.2倍、横倍率3.
2倍と1−1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の二軸配向フィ
ルムを得た。
Example 3 Among the stretching ratios of Example 2, the longitudinal magnification was 4.2 times and the horizontal magnification was 3.
A biaxially oriented film with a thickness of 7.2 μm was obtained in the same manner as in Example 2, except that the heat setting temperature after the 2-fold and 1-1 transverse stretching was 235° C.

目とも非常に良好であった。The eyes were also very good.

実施例4 実施例1のポリマーを用(・た他は、実施例3とr=+
−延伸・熱固定条件で処理し、浮さ7.3μmの二軸配
向フィルムを得た。
Example 4 Using the polymer of Example 1 (other than that, Example 3 and r=+
- Processed under stretching and heat setting conditions to obtain a biaxially oriented film with a float of 7.3 μm.

その結果は表−1に示す如くでいずれの項目とも良好で
あった。
The results are shown in Table 1, and all items were good.

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
二軸配向フィルムを得た。
Example 5 A biaxially oriented film having a thickness of 7.5 μm was obtained by stretching and heat setting under the same conditions as in Example 2 except that the heat setting temperature was 215° C.

その結果は表−1に示す如くで、いずれの項目とも良好
であった。
The results are shown in Table 1, and all items were good.

実施例6 実施倒置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It%とを用い。
Example 6 During inversion, 0.45% by weight of calcium carbonate (average particle size 1.5 μm) and silica (average particle size 0) were added as lubricants.
.. 6 μm) with 0.25 weight It%.

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と同様に行って厚み7.2μm
の二軸配向フィルムを得た。
Stretched 4.5 times in the machine direction, followed by 3.6 times in the transverse direction.
The thickness was 7.2 μm by carrying out the same procedure as in Example 1 except for double stretching.
A biaxially oriented film was obtained.

その結果は表−IK示す如くで、いずれの項目も良好で
あった。
The results were as shown in Table IK, and all items were good.

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o、51μm)を0.4
1i量チを用いた他は、実施例6と同様に行って厚み7
.2μmの二軸配向フィルムをイ0た。
Example 7 In Example 6, silica (average particle size 2.0 μm) was added to 0.0 μm.
1% by weight and 0.4% kaolin (average particle size o, 51 μm)
A thickness of 7 was obtained in the same manner as in Example 6, except that a 1i quantity was used.
.. A 2 μm biaxially oriented film was prepared.

その結果は表−IK示す如くで、いずれの項目も良好で
あった。
The results were as shown in Table IK, and all items were good.

比較例1 実施例1で得た未延伸フィルムを75℃にて予熱し、更
に低速、高速p−ルの間で15m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
のp−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、llo’cKて3.8倍に横力向
1c延伸した。得られた二軸延伸フィルムを更に210
℃にて15秒間熱固定して厚み7.7μmのフィルムを
得た。
Comparative Example 1 The unstretched film obtained in Example 1 was preheated at 75°C, and further heated with one infrared heater with a surface temperature of 900°C from 15 m above between low speed and high speed rollers. The film was stretched 3.3 times by the difference in surface speed of a high-speed roller, then fed to a stenter, and stretched 3.8 times in the transverse force direction 1c by 10'cK. The obtained biaxially stretched film was further
The film was heat-set at ℃ for 15 seconds to obtain a film having a thickness of 7.7 μm.

得られた二軸配向フィ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っ
たが、フィ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った。
The evaluation results for each item after coating the obtained biaxially oriented film and the ink layer to form a ribbon are as shown in Table 2, and the ink transferability and runnability were at a reasonably good level. , the degree of film deformation and print clarity were poor, and the overall evaluation was also poor.

比較例2 実施例2で得た未延伸フィルムを、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の二軸配向フィルムを得た。
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 a thickness of 7
.. A biaxially oriented film of 7 μm was obtained.

得られた二軸配向フィ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
劣るものであった。
The evaluation results of the obtained biaxially oriented film and ribbon are shown in Table-
As shown in No. 2, the ink transferability and runnability were at a better level than in Comparative Example 1, but the overall evaluation was poor.

比較例3 添加滑剤としてカオリン(平均粒径0,5μmル)を対
ポリマ−0,5]llLi1%添加して得た未延伸フィ
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の二軸配向フィ
ルムを得た。
Comparative Example 3 An unstretched film obtained by adding 1% of kaolin (average particle size 0.5 μm) to the polymer as an additive lubricant was adjusted to a longitudinal stretching ratio of 3.6 times in Comparative Example 1. 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 heat setting temperature was 230° C.

得られた二軸配回フィルムの各項目は表−2に示した如
くであり、表面突起分布曲庫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
−っだ。
The characteristics of the obtained biaxially distributed film are as shown in Table 2, and the surface protrusion distribution curvature was below the preferred range, the ink transferability and runnability were poor, and the overall evaluation was poor. -That's it.

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ィルム
を、比較装置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
フィルムを得た。
Comparative Example 4 Calcium carbonate (average particle size 1.5 μm) as added lubricant
An unstretched film obtained by adding 0.8% by weight of 0.8% by weight to the polymer was subjected to a comparative device with a longitudinal stretching ratio of 4.2 times, a horizontal stretching ratio of 3.5 times, and a heat setting temperature of 230 ° C. The other conditions were the same as in Comparative Example 1 to obtain a biaxially oriented film with a thickness of 7.5 μm.

得られた二軸配向フィルムの各項目の評価結果は表−2
に示す如くであり、異面突起分布曲数が粗すぎて印字鮮
明性は悪く、総合評価は劣ったものであった。
The evaluation results for each item of the obtained biaxially oriented film are shown in Table 2.
As shown in FIG. 2, the number of curves in the distribution of different surface protrusions was too coarse, the print clarity was poor, and the overall evaluation was poor.

比較例5 添加滑剤として炭酸カルシウム(平均粒径1.5μm)
を対ポリマー当90.4N量条添加させて得た厚さ15
0μmの未延伸フィルムを、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。
Comparative Example 5 Calcium carbonate (average particle size 1.5 μm) as added lubricant
Thickness 15 obtained by adding 90.4 N per polymer
An unstretched film of 0 μm was heated at low speed under the conditions of Comparative Example 1 using an infrared heater with a surface temperature of 750°C.

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’Cで熱固定して厚さ7.5μmの二軸配向フィ
ルムを得た。
Stretched 3.0 times in the longitudinal direction at the surface speed ratio of high-speed rolls,
Next, it was stretched in the transverse direction at a draw ratio of 3.7 times in hot air at 95°C, and further stretched in the machine direction again at a draw ratio of 1.8 times by heating with an infrared heater with a surface temperature of 1000°C, and then 220' C. to obtain a biaxially oriented film with a thickness of 7.5 μm.

得られた二軸配向フィルムの各項目は表−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ィルム
が縦方向に裂けてしまい。
The items of the obtained biaxially oriented film are as shown in Table 2. When printing with a printer, the film was torn in the vertical direction due to the printing pressure.

鮮明な印字ができず総合評価は劣ったものであった。Clear printing was not possible and the overall evaluation was poor.

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の二軸配向フィルムを得た
Comparative Example 6 A biaxially oriented film with a thickness of 7.5 μm was obtained by processing under the same conditions as in Comparative Example 2 except that the heat setting temperature was 180° C.

得られた二軸配向フィルムの各項目は表−2に示す如く
であり、印字圧力によりフィ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
悪いものであった。
The properties 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. Ta.

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

図−1は転写リボンの走行性の測定装置の模式図−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ィルム表面の突起高さ
くY:μm)と突起の数(X:ケ/−)の関係を示す図
である。
FIG. 1 is a schematic diagram of an apparatus for measuring transfer ribbon runnability, and 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) determined by a three-dimensional roughness meter and the number of protrusions (X: ke/-).

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ィルム
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
であって、該フィルムは縦方向のヤング率が450〜8
00kg/mm^2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、更に該フィルムの転
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/mm^2)と突起高さ(X:μm)との関
係を表わす突起分布曲線がlog_1_0Y>1.3の
領域において下記式(1) log_1_0Y=−1.8X+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) log_1_0Y≧−3.6X+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、ポリエステルフィ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/mm^2)と突起高さ(h:μm)が 1.5≧h>1.0・・・・・・10ケ/mm^2以下
1.0≧h>0.75・・・・・・1〜30ケ/mm^
20.75≧h>0.5・・・・・・15〜120ケ/
mm^20.5≧h>0.25・・・・・・80ケ/m
m^2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、ポリエステルフィ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15
0%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 a printer 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 8.
00kg/mm^2 and 150 in the vertical and horizontal directions
The heat shrinkage rate at °C is 7% or less, and the surface of the film on which the transfer ink layer is provided has a number of protrusions (Y: x/mm^2) and a protrusion height (X: In the area where log_1_0Y>1.3, the protrusion distribution curve representing the relationship with μm) is expressed by the following formula (1) log_1_0Y=-1.8X+3.9 (
The maximum value of the protrusion distribution and the curve of the portion exceeding the maximum value that do not intersect the line represented by 1) are expressed by the following formula (2) log_1_0Y≧−3.6X+2.8 (
2) A transfer ribbon for a printer, characterized by having surface characteristics within a range that satisfies the following. 2. The surface of the polyester film on which the transfer ink layer is to be provided has a number of protrusions (ke/mm^2) and a protrusion height (h: μm) measured with a multiple interference reflection microscope (Tl monochromatic light) of 1.5≧h> 1.0...10 pieces/mm^2 or less 1.0≧h>0.75...1~30 pieces/mm^
20.75≧h>0.5...15-120 pieces/
mm^20.5≧h>0.25...80 pieces/m
The transfer ribbon for a printer according to claim 1, which satisfies m^2 or more. 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 15% lower than the initial value.
The transfer ribbon for a printer according to claim 1 or 2, wherein the transfer ribbon has a content of less than 0%.
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 true JPS62193889A (en) 1987-08-26
JPH0453197B2 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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JPH0218090A (en) * 1988-07-07 1990-01-22 Diafoil Co Ltd Thermal transfer polyphenylene sulfide film
JPH0225396A (en) * 1988-07-14 1990-01-26 Diafoil Co Ltd Film for thermal transfer
JPH0239998A (en) * 1988-07-29 1990-02-08 Diafoil Co Ltd Polyethylene naphthalate film for thermal transfer
JPH0247094A (en) * 1988-08-10 1990-02-16 Diafoil Co Ltd Transfer material for printer
JPH0247093A (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
EP0356904A2 (en) * 1988-08-31 1990-03-07 Diafoil Hoechst Co., Ltd Transfer material for use with printer
EP0383267A2 (en) * 1989-02-15 1990-08-22 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer sheet
JPH02219695A (en) * 1989-02-21 1990-09-03 Diafoil Co Ltd Polyester film for thermosensitive transfer
JPH02252583A (en) * 1989-03-27 1990-10-11 Diafoil Co Ltd Polyester film for thermal transfer
US5250495A (en) * 1989-02-15 1993-10-05 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer recording process
WO2002043944A1 (en) * 2000-12-01 2002-06-06 Teijin Limited Biaxially oriented polyester film
JP2016052781A (en) * 2015-09-24 2016-04-14 大日本印刷株式会社 Polyester resin composition laminate
US11186701B2 (en) * 2019-09-02 2021-11-30 Toyobo Co., Ltd. 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 Heat transfer material
JPS60104395A (en) * 1983-11-11 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
JPS60104392A (en) * 1983-11-10 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
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JPS60217194A (en) * 1984-04-13 1985-10-30 Toray Ind Inc Transfer material for printer

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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 Heat transfer material
JPS60104392A (en) * 1983-11-10 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
JPS60104393A (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
JPS60174694A (en) * 1984-02-20 1985-09-07 Toray Ind Inc Thermal transfer material
JPS60217194A (en) * 1984-04-13 1985-10-30 Toray Ind Inc Transfer material for printer

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0218090A (en) * 1988-07-07 1990-01-22 Diafoil Co Ltd Thermal transfer polyphenylene sulfide film
JPH0225396A (en) * 1988-07-14 1990-01-26 Diafoil Co Ltd Film for thermal transfer
JPH0239998A (en) * 1988-07-29 1990-02-08 Diafoil Co Ltd Polyethylene naphthalate film for thermal transfer
JPH0247094A (en) * 1988-08-10 1990-02-16 Diafoil Co Ltd Transfer material for printer
JPH0247093A (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
EP0356904A2 (en) * 1988-08-31 1990-03-07 Diafoil Hoechst Co., Ltd Transfer material for use with printer
US5130293A (en) * 1989-02-15 1992-07-14 Dai Nippon Insatsu Kabushiki Kaisha Heat transfer sheet
EP0383267A2 (en) * 1989-02-15 1990-08-22 Dai Nippon Insatsu Kabushiki Kaisha Heat 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
JPH02252583A (en) * 1989-03-27 1990-10-11 Diafoil Co Ltd Polyester film for thermal transfer
WO2002043944A1 (en) * 2000-12-01 2002-06-06 Teijin Limited Biaxially oriented polyester film
US6761968B2 (en) 2000-12-01 2004-07-13 Teijin Limited Biaxially oriented polyester film
JP2016052781A (en) * 2015-09-24 2016-04-14 大日本印刷株式会社 Polyester resin composition laminate
US11186701B2 (en) * 2019-09-02 2021-11-30 Toyobo Co., Ltd. Biaxially oriented polyester film

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