JP2581270B2 - Thermal transfer ribbon - Google Patents
Thermal transfer ribbonInfo
- Publication number
- JP2581270B2 JP2581270B2 JP2149116A JP14911690A JP2581270B2 JP 2581270 B2 JP2581270 B2 JP 2581270B2 JP 2149116 A JP2149116 A JP 2149116A JP 14911690 A JP14911690 A JP 14911690A JP 2581270 B2 JP2581270 B2 JP 2581270B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- thermal transfer
- ribbon
- temperature
- 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.)
- Expired - Lifetime
Links
- 238000012546 transfer Methods 0.000 title claims description 33
- 229920006267 polyester film Polymers 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 9
- 239000010410 layer Substances 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 7
- 230000037303 wrinkles Effects 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000003746 surface roughness Effects 0.000 description 5
- -1 Polyethylene terephthalate Polymers 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000007757 hot melt coating Methods 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- BWVAOONFBYYRHY-UHFFFAOYSA-N [4-(hydroxymethyl)phenyl]methanol Chemical compound OCC1=CC=C(CO)C=C1 BWVAOONFBYYRHY-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000003141 anti-fusion Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000006103 coloring component Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000002335 surface treatment layer Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Impression-Transfer Materials And Handling Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、熱転写プリンター用転写材に用いられる印
字性能に優れた熱転写用リボンに関するものである。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermal transfer ribbon excellent in printing performance used for a transfer material for a thermal transfer printer.
熱転写プリンター用リボンのベースフィルムとして
は、表面粗さを規定したもの(特開昭62−299389号公
報、特開昭62−193889号公報)や、材質と縦方向のヤン
グ率を規定したもの(特開昭62−111719号公報)が知ら
れている。As a base film of a ribbon for a thermal transfer printer, a film having a specified surface roughness (Japanese Patent Application Laid-Open No. 62-299389 and Japanese Patent Application Laid-Open No. 62-193889), a material having a specified material and a Young's modulus in the longitudinal direction ( JP-A-62-111719) is known.
しかし、近年印字速度の高速化が求められるようにな
るにつれて、印字時のサーマルヘッドの温度が高くなっ
た結果、熱転写プリンターリボンの受ける熱量が多くな
った。このため、リボンの基材に使用されているフィル
ムの変形が大きくなり、印字の際に印字が不鮮明になっ
たり、リボンに皺が発生して、極端な場合には全く印字
不能になる等のトラブルを生じ、この改善が必要であっ
た。However, in recent years, as the printing speed has been required to be higher, the temperature of the thermal head at the time of printing has increased, and as a result, the amount of heat received by the thermal transfer printer ribbon has increased. For this reason, the deformation of the film used for the base material of the ribbon becomes large, and the printing becomes unclear at the time of printing, or wrinkles are generated on the ribbon, and in an extreme case, printing becomes impossible at all. A trouble occurred and this improvement was necessary.
本発明は、かかる問題点を改善し印字性に優れた熱転
写用リボンを提供することを目的とする。It is an object of the present invention to improve such a problem and to provide a thermal transfer ribbon excellent in printability.
本発明は、二軸配向ポリエステルフィルムを基材層と
し、該基材層の片面に熱転写インキ層が設けられた熱転
写用リボンにおいて、該二軸配向ポリエステルフィルム
の横方向の温度寸法変化曲線を測定したときに、該曲線
の勾配が負から正に変化する点が存在し、該点における
温度が200℃以上であり、かつ該点におけるフィルムの
原長に対する寸法変化率が−5〜+5%であることを特
徴とする熱転写用リボン、を要旨とする。The present invention relates to a thermal transfer ribbon in which a biaxially oriented polyester film is used as a base material layer and a thermal transfer ink layer is provided on one surface of the base material layer, and measures a transverse temperature dimensional change curve of the biaxially oriented polyester film. When there is a point at which the slope of the curve changes from negative to positive, the temperature at that point is 200 ° C. or more, and the dimensional change rate with respect to the original length of the film at the point is −5 to + 5%. The present invention provides a ribbon for thermal transfer, which is characterized in that there is a feature.
本発明において、ポリエステルとは、ジカルボン酸成
分とジオール成分とから縮合法によって得られるエステ
ル基を含む縮重合体である。ジカルボン酸成分として
は、テレフタル酸、イソフタル酸、フタル酸、2,6−ナ
フタレンジカルボン酸、アジピン酸、セバシン酸などを
例示することができ、ジオール成分としては、エチレン
グリコール、ジエチレングリコール、ブタンジオール、
ヘキサンジオール、ネオペンチルグリコール、p−キシ
レングリコール、1,4−シクロヘキサンジメタノール、
平均分子量150〜20000のポリアルキレングリコールなど
を例示することができる。In the present invention, the polyester is a condensation polymer containing an ester group obtained from a dicarboxylic acid component and a diol component by a condensation method. Examples of the dicarboxylic acid component include terephthalic acid, isophthalic acid, phthalic acid, 2,6-naphthalenedicarboxylic acid, adipic acid, and sebacic acid.The diol component includes ethylene glycol, diethylene glycol, butanediol, and the like.
Hexanediol, neopentyl glycol, p-xylene glycol, 1,4-cyclohexanedimethanol,
Examples thereof include polyalkylene glycols having an average molecular weight of 150 to 20,000.
また、本発明に用いられるポリエステルには、粒径0.
3〜3μmの二酸化ケイ素、炭酸カルシウム、カオリ
ン、フッ素樹脂粒子、シリコーン粒子などの無機または
有機滑剤を0.1〜1.0重量%含んでいたほうがよい。これ
らの無機または有機滑剤を添加することにより、表面の
平均粗さが0.03〜0.3μmの二軸配向ポリエステルフィ
ルムを得ることができる。フィルムの平均表面粗さが0.
03μmより小さいと、十分な滑り性が得られず、巻き取
ることが困難になる。また、平均表面粗さが0.3μmよ
り大きいと、熱転写プリンターで印字する際、熱伝導が
悪化し、印字が不鮮明となる。添加する無機または有機
滑剤の粒径が0.3μm小さいと、十分大きな表面粗さを
得ることができず、3μmより大きいと、延伸工程でフ
ィルム破れが発生しやすくなる。Further, the polyester used in the present invention has a particle size of 0.1.
It is preferable to contain 0.1 to 1.0% by weight of an inorganic or organic lubricant such as silicon dioxide, calcium carbonate, kaolin, fluororesin particles, or silicone particles of 3 to 3 μm. By adding these inorganic or organic lubricants, a biaxially oriented polyester film having an average surface roughness of 0.03 to 0.3 μm can be obtained. The average surface roughness of the film is 0.
If it is smaller than 03 μm, sufficient slip properties cannot be obtained, and it becomes difficult to wind up. On the other hand, when the average surface roughness is larger than 0.3 μm, when printing with a thermal transfer printer, heat conduction is deteriorated and the printing becomes unclear. If the particle size of the inorganic or organic lubricant to be added is smaller than 0.3 μm, a sufficiently large surface roughness cannot be obtained, and if it is larger than 3 μm, the film tends to be broken in the stretching step.
また、本発明に用いられるポリエステルには、必要に
応じて、安定剤、着色剤、酸化防止剤、その他の添加剤
等を含有してもよい。Further, the polyester used in the present invention may contain a stabilizer, a colorant, an antioxidant, other additives, and the like, if necessary.
本発明において、フィルムの横方向の温度寸法変化曲
線(以下「TMA曲線」ともいう)とは、フィルムの横方
向の両端を把持し、ある特定の一定荷重を加えながら、
一定の昇温速度でフィルムを加熱し、その温度を横軸
に、フィルムの原長に対する寸法変化率を縦軸にとり描
かせた曲線をいう。In the present invention, the lateral temperature dimensional change curve of the film (hereinafter also referred to as “TMA curve”) refers to a film in which both ends in the lateral direction of the film are gripped and a specific constant load is applied.
A curve in which a film is heated at a constant rate of temperature increase, and the temperature is plotted on the horizontal axis, and the dimensional change rate of the film relative to the original length is plotted on the vertical axis.
本発明に用いる二軸配向ポリエステルフィルムは、そ
のフィルムの横方向の温度寸法変化曲線を測定したとき
に、その曲線の勾配が負から正に変化する点(以下「極
小点」という)を有し、該極小点における温度(以下単
に「極小点の温度」ともいう)が200℃以上であり、該
極小点におけるフィルムの原長に対する寸法変化率(以
下単に「極小点の寸法変化率」ともいう)が−5〜+5
%である。極小点の温度が200℃よりも低いか、または2
00℃以上でも極小点の寸法変化率が−5%より低いと、
印字時のフィルムの収縮が大きくなりフィルムに皺が発
生するので、印字ができなくなる。また、極小点の寸法
変化率が+5%よりも大きいと、ベースフィルムにイン
ク層や、背面処理層を塗工する際にかかる熱によるフィ
ルムの伸びが大きくなるので塗工時にフィルムがたる
み、塗布斑を発生しやすい。The biaxially oriented polyester film used in the present invention has a point at which the gradient of the curve changes from negative to positive (hereinafter referred to as "minimum point") when a temperature dimensional change curve in the transverse direction of the film is measured. The temperature at the minimum point (hereinafter, also simply referred to as “minimum point temperature”) is 200 ° C. or more, and the dimensional change rate with respect to the original length of the film at the minimum point (hereinafter, also simply referred to as “dimensional change rate at the minimum point”) ) Is -5 to +5
%. Minimum point temperature below 200 ° C or 2
When the dimensional change rate of the minimum point is lower than −5% even at 00 ° C. or higher,
Since the shrinkage of the film at the time of printing increases and wrinkles occur on the film, printing cannot be performed. On the other hand, if the dimensional change rate of the minimum point is larger than + 5%, the film is stretched by the heat applied when the ink layer or the back surface treatment layer is applied to the base film. Spots are likely to occur.
本発明に用いる二軸配向ポリエステルフィルムの厚さ
は2〜10μmが好ましく、かつ縦方向のF−5値は11〜
15kg/mm2が好ましい。厚さが10μmを超えると、熱伝達
に時間がかかり、高速印字に好適ではない。逆に、厚さ
が2μm未満であると、強力が低く、加工適性に劣り好
ましくない。F−5値が11kg/mm2未満であると、リボン
の走行時にリボンが伸びて印字が不鮮明になったり、皺
が発生しやすくなる。F−5値が15kg/mm2を超えると、
TMA曲線の極小点が適性範囲を外れるため、印字時に皺
が発生する。The thickness of the biaxially oriented polyester film used in the present invention is preferably 2 to 10 μm, and the F-5 value in the longitudinal direction is 11 to 10 μm.
15 kg / mm 2 is preferred. If the thickness exceeds 10 μm, it takes time for heat transfer, which is not suitable for high-speed printing. Conversely, if the thickness is less than 2 μm, the strength is low and the workability is poor, which is not preferable. When the F-5 value is less than 11 kg / mm 2 , the ribbon is stretched during running of the ribbon, so that printing becomes unclear or wrinkles are easily generated. When F-5 value exceeding 15 kg / mm 2,
Since the minimum point of the TMA curve is out of the appropriate range, wrinkles occur during printing.
次に、本発明に用いる二軸配向ポリエステルフィルム
の製造方法について述べる。ただし、本発明は以下に述
べる製造方法に限定されるものではない。Next, a method for producing the biaxially oriented polyester film used in the present invention will be described. However, the present invention is not limited to the manufacturing method described below.
まず、ポリエステルを溶融し、スリット状のダイによ
りフィルム状に成型する。このフィルムを表面温度20〜
70℃のキャスティングドラムに巻き付けて冷却固化し未
延伸フィルムとする。その未延伸フィルムを多段階の高
倍率延伸、すなわち2以上の複数の区間で80〜130℃に
加熱し、それぞれロール間の周速差により合計倍率が4
〜7倍になるように延伸した後、90〜120℃で3〜4倍
で横方向に延伸する。次いで210〜240℃にて5〜20秒間
熱処理を行なったのち、熱処理温度より10〜20℃低い温
度で横方向に3〜10%収縮させながら再熱処理を行ない
二軸配向ポリエステルフィルムを得る。First, the polyester is melted and molded into a film by a slit die. This film has a surface temperature of 20 ~
It is wound around a casting drum at 70 ° C and solidified by cooling to form an unstretched film. The unstretched film is stretched in multiple stages at a high magnification, that is, heated to 80 to 130 ° C. in two or more sections, and a total magnification of 4 is obtained by a difference in peripheral speed between rolls.
After stretching to 77 times, the film is stretched in the transverse direction at 90 to 120 ° C. at 3 to 4 times. Next, after a heat treatment at 210 to 240 ° C. for 5 to 20 seconds, a re-heat treatment is performed at a temperature lower by 10 to 20 ° C. while shrinking by 3 to 10% in a transverse direction to obtain a biaxially oriented polyester film.
本発明において、熱転写インク層は、特に限定される
ものではなく、公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、可塑剤、分散剤などを適量添加して
構成される。上記主成分の具体例としては、バインダー
成分として、カルナウバワックス、パラフィンワックス
など公知のワックス類や低融点の各種高分子物質が用い
られ、着色剤としては、カーボンブラック主体とし、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。また、熱転写インキ層は、昇華性の染料を含んでい
てもよい。In the present invention, the thermal transfer ink layer is not particularly limited, and a known one can be used. That is, a binder component, a coloring component, and the like are used as main components, and a softener, a plasticizer, a dispersant, and the like are added in appropriate amounts as needed. Specific examples of the main component include, as binder components, known waxes such as carnauba wax and paraffin wax and various low-melting polymer materials, and as a coloring agent, mainly carbon black, and other various dyes Alternatively, an organic or inorganic pigment is used. Further, the thermal transfer ink layer may contain a sublimable dye.
熱転写インキ層を基材層の片面に設ける方法として
は、公知の方法、例えばホットメルト塗工、溶剤を添加
した状態でグラビア、リバース、スリットダイ方式など
の溶液塗工方法などを用いることができる。なお、サー
マルヘッド部のスティックキングを防ぐために、熱転写
インキ層の設けていない側に、シリコーン樹脂、メラミ
ン樹脂、フッ素樹脂、シリコーンオイル、鉱物オイル等
の融着防止層を設けるのがよい。さらに、融着防止層を
設けるのは、未延伸または縦延伸後に行なうほうが望ま
しい。このようにすることにより、転写リボンに加工す
る際の熱履歴を減らすことができ、該二軸配向ポリエス
テルフィルムの温度寸法変化特性を本発明の範囲に保つ
ことが容易になる。As a method of providing the thermal transfer ink layer on one side of the base material layer, a known method, for example, hot melt coating, gravure with a solvent added, reverse, a solution coating method such as a slit die method and the like can be used. . In order to prevent sticking of the thermal head portion, it is preferable to provide a fusion preventing layer such as a silicone resin, a melamine resin, a fluororesin, a silicone oil, or a mineral oil on the side where the thermal transfer ink layer is not provided. Further, it is desirable to provide the anti-fusion layer after unstretching or after longitudinal stretching. This makes it possible to reduce the heat history when processing into a transfer ribbon, and to easily maintain the temperature dimensional change characteristics of the biaxially oriented polyester film within the range of the present invention.
本発明で規定する特性値の測定方法と評価方法を以下
に述べる。The method for measuring and evaluating the characteristic value specified in the present invention will be described below.
(1)温度寸法変化曲線 PERKIN ELMER社製のTMA(サーマルメカニカルアナラ
イザー)を用いて測定する。ただし、昇温速度は10℃/
分、荷重は200g/mm2とした。(1) Temperature dimension change curve Measured using TMA (thermal mechanical analyzer) manufactured by PERKIN ELMER. However, the heating rate is 10 ° C /
And the load was 200 g / mm 2 .
(2)F−5値 ASTM−D−882によるテンシロン型引っ張り試験機に
試幅10mm、試長100mmとなるようにセットし、引っ張り
速度200mm/分、温度20℃、湿度65%RHの条件でフィルム
の5%伸長の対応する強度を測定する。(2) F-5 value The sample was set on a Tensilon-type tensile tester according to ASTM-D-882 so as to have a test width of 10 mm and a test length of 100 mm, under the conditions of a pulling speed of 200 mm / min, a temperature of 20 ° C, and a humidity of 65% RH. The corresponding strength of the 5% elongation of the film is measured.
(3)印字性 オークス社製のバーコードプリンター(BC−8)で黒
ベタを印字して、次の基準により、印字性を評価した。(3) Printability Black solid was printed by a bar code printer (BC-8) manufactured by Oaks Co., Ltd., and printability was evaluated according to the following criteria.
○:鮮明に印字 △:印字にピッチずれが生じる。:: Clear printing Δ: Pitch shift occurs in printing.
×:リボンに皺が入り印字が乱れる。×: Wrinkles appear on the ribbon and printing is disturbed.
××:ホットメルト塗工時にフィルムに皺が入り、転写
インクが均一に塗布できない。XX: Wrinkles are formed on the film during hot melt coating, and the transfer ink cannot be applied uniformly.
以下、実施例に基づいて本発明をさらに詳しく説明す
る。ただし、本発明は以下の実施例に限定されるもので
はない。Hereinafter, the present invention will be described in more detail based on examples. However, the present invention is not limited to the following examples.
実施例1 35℃のo−クロロフェノール溶融で測定した固有粘度
が0.61で、粒径が1.0μmの二酸化ケイ素を0.2重量%含
有したポリエチレンテレフタレートを、押し出し機とT
ダイでシート状に溶融押し出し、水冷ドラムに密着させ
て冷却固化し、厚さ30〜120μmの非晶質シートを得
た。多段縦延伸装置、すなわち第1段階が125℃で2.2
倍、第2段が125℃で1.1倍、第3段が115℃で2.3倍、合
計5.6倍の3段階縦延伸を行なった。Example 1 Polyethylene terephthalate containing 0.2% by weight of silicon dioxide having an intrinsic viscosity of 0.61 and a particle size of 1.0 μm, measured by melting o-chlorophenol at 35 ° C., was extruded with an extruder and T
It was melt-extruded into a sheet shape by a die, and was adhered to a water-cooled drum to be cooled and solidified to obtain an amorphous sheet having a thickness of 30 to 120 μm. Multi-stage longitudinal stretching equipment, ie the first stage is 2.2 ° C at 125 ° C
Three-stage longitudinal stretching was carried out at 1.1 times at 125 ° C in the second stage and 2.3 times at 115 ° C in the third stage, a total of 5.6 times.
この縦延伸後のフィルムの片面に、融着防止層として
下記組成の塗剤を乾燥後の塗膜厚みが0.5μmになるよ
うにグラビアコーターで塗工した後、テンターオーブン
で110℃、3.8倍の横延伸を行なった。次に、225℃で固
定長で緊張熱処理を行なった後、210℃で横方向に6%
収縮させながら再熱処理を行ない、厚さが5μm(ただ
し塗膜を除く)の二軸配向ポリエステルフィルムを得
た。On one side of this longitudinally stretched film, after coating with a gravure coater so that the coating thickness after drying is 0.5 μm as a fusion-preventing layer, the coating thickness after drying is 110 ° C., 3.8 times in a tenter oven. In the transverse direction. Next, after performing a tension heat treatment at a fixed length at 225 ° C., 6% in a lateral direction at 210 ° C.
Re-heat treatment was performed while shrinking to obtain a biaxially oriented polyester film having a thickness of 5 μm (excluding the coating film).
(塗剤の組成) アクリル酸エステル 14.0重量% アミノ変性シリコーン 5.9重量% イソシアネート 0.1重量% 水 80.0重量% 得られた二軸延伸配向ポリエステルフィルムについ
て、縦方向のF−5値、および横方向の温度寸法変化曲
線を測定し、極小点の温度および極小点の寸法変化率を
求めた。なお、第1図は、この実施例の二軸延伸配向ポ
リエステルフィルムの横方向の温度寸法変化曲線であ
り、点Aは極小点である。(Composition of coating agent) Acrylic ester 14.0% by weight Amino-modified silicone 5.9% by weight Isocyanate 0.1% by weight Water 80.0% by weight About the obtained biaxially oriented polyester film, the F-5 value in the longitudinal direction and the temperature in the transverse direction The dimensional change curve was measured, and the temperature at the minimum point and the dimensional change rate at the minimum point were determined. FIG. 1 is a lateral temperature dimensional change curve of the biaxially oriented polyester film of this example, and point A is a minimum point.
次に、下記組成の転写インクを、塗膜厚みが3.5μm
になるようにホットメルトコーターで融着防止層とは反
対面に塗工し、転写リボンを作製した。Next, a transfer ink having the following composition was applied to a coating having a thickness of 3.5 μm.
Was applied to the surface opposite to the anti-fusing layer using a hot melt coater to obtain a transfer ribbon.
(転写インクの組成) カルナウバワックス 60.6重量% マイクロクリスタリンワックス 18.2重量% 酢酸ビニル・エチレン共重合体 0.1重量% カーボンブラック 21.1重量% 作製した熱転写用リボンについて印字性を評価した。
評価結果を第1表に示す。(Composition of Transfer Ink) Carnauba wax 60.6% by weight Microcrystalline wax 18.2% by weight Vinyl acetate / ethylene copolymer 0.1% by weight Carbon black 21.1% by weight Printability of the produced thermal transfer ribbon was evaluated.
Table 1 shows the evaluation results.
実施例2 35℃のo−クロロフェノール溶融で測定した固有粘度
が0.61で、粒径が1.0μmの二酸化ケイ素を0.2重量%含
有したポリエチレンテレフタレートを、押し出し機とT
ダイでシート状に溶融押し出し、水冷ドラムに密着させ
て冷却固化し、厚さ30〜120μmの非晶質シートを得
た。多段縦延伸装置、すなわち第1段階が125℃、2.1
倍、第2段が125℃で1.1倍、第3段が115℃で2.6倍、合
計6.0倍の3段階縦延伸を行なった後、テンターオーブ
ンで110℃、3.8倍の横延伸を行なった。次に、230℃で
固定長で緊張熱処理を行なった後、210℃で横方向に6
%収縮させながら再熱処理を行ない、厚さが5μmの二
軸配向ポリエステルフィルムを得た。このフィルムの片
面に融着防止層として下記組成の塗剤を乾燥後の塗膜厚
みが0.2μmになるようにグラビアコーターで塗工し、8
0℃で乾燥を行なった。Example 2 Polyethylene terephthalate containing 0.2% by weight of silicon dioxide having an intrinsic viscosity of 0.61 and a particle size of 1.0 μm measured by melting o-chlorophenol at 35 ° C. was extruded with an extruder and T
It was melt-extruded into a sheet shape by a die, and was adhered to a water-cooled drum to be cooled and solidified to obtain an amorphous sheet having a thickness of 30 to 120 μm. Multi-stage longitudinal stretching equipment, ie the first stage is 125 ° C, 2.1
After performing three-stage longitudinal stretching at a temperature of 125 ° C. in the second stage and 2.6 times at 115 ° C. in the third stage, and a total of 6.0 times, a transverse stretching of 110 ° C. and 3.8 times in a tenter oven was performed. Next, after performing tension heat treatment at 230 ° C. with a fixed length,
% Heat shrinkage to obtain a biaxially oriented polyester film having a thickness of 5 μm. One side of this film was coated with a coating composition having the following composition as a fusion preventing layer using a gravure coater so that the coating film thickness after drying was 0.2 μm.
Drying was performed at 0 ° C.
(塗剤の組成) アクリル酸エステル 14.0重量% アミノ変性シリコーン 5.9重量% イソシアネート 0.1重量% トルエン 80.0重量% 次に、実施例1と同様にして転写インクを塗工して熱
転写用リボンを作製し評価した。評価結果を第1表に示
す。(Composition of coating agent) Acrylic ester 14.0% by weight Amino-modified silicone 5.9% by weight Isocyanate 0.1% by weight Toluene 80.0% by weight Next, a transfer ink was applied in the same manner as in Example 1 to prepare a thermal transfer ribbon and evaluated. did. Table 1 shows the evaluation results.
比較例1 90℃で2.75倍で縦延伸した後、100℃、3.4倍で横延伸
し、130℃、2.0倍で再縦延伸し、次いで220℃緊張熱処
理を行なったほかは、実施例1と同じ方法で熱転写用リ
ボンを作製し評価した。評価結果を第1表に示す。Comparative Example 1 After stretching longitudinally at 2.75 times at 90 ° C., stretching transversely at 100 ° C. and 3.4 times, stretching longitudinally again at 130 ° C. and 2.0 times, and then performing a tensile heat treatment at 220 ° C. A ribbon for thermal transfer was produced and evaluated in the same manner. Table 1 shows the evaluation results.
比較例2 実施例1と同じ方法で縦延伸と横延伸および緊張熱処
理を行った後、再熱処理を行なわずに転写リボンを作製
し評価した。評価結果を第1表に示す。Comparative Example 2 After performing longitudinal stretching, transverse stretching, and tension heat treatment in the same manner as in Example 1, a transfer ribbon was prepared and evaluated without performing reheat treatment. Table 1 shows the evaluation results.
比較例3 実施例1と同じ方法で縦延伸と横延伸および緊張熱処
理を行った後、215℃で横方向に12%収縮させながら再
熱処理を行ない熱転写用リボンを作製し評価した。評価
結果を第1表に示す。Comparative Example 3 After performing longitudinal stretching, transverse stretching, and tension heat treatment in the same manner as in Example 1, the heat treatment was performed again while shrinking 12% in the horizontal direction at 215 ° C., and a thermal transfer ribbon was produced and evaluated. Table 1 shows the evaluation results.
〔発明の効果〕 本発明の熱転写用リボンは、印字の際に皺が発生する
ことがなく、鮮明な印字を得ることができる。 [Effect of the Invention] The thermal transfer ribbon of the present invention can obtain clear printing without wrinkles during printing.
第1図は実施例1で得られた二軸延伸配向ポリエステル
フィルムの横方向の温度寸法変化曲線を示す。図中、点
Aは曲線の勾配が負から正に変化する点(極小点)であ
り、点Bは極小点における温度を示し、点Cは極小点に
おけるフィルムの原長に対する寸法変化率を示す。FIG. 1 shows a temperature dimensional change curve in a lateral direction of the biaxially oriented polyester film obtained in Example 1. In the drawing, a point A is a point (minimum point) where the slope of the curve changes from negative to positive, a point B indicates a temperature at the minimum point, and a point C indicates a dimensional change rate with respect to the original length of the film at the minimum point. .
フロントページの続き (56)参考文献 特開 昭62−95289(JP,A) 特開 平2−43022(JP,A) 特開 平1−186380(JP,A) 特開 昭63−237989(JP,A) 特開 昭63−170018(JP,A) 特開 平1−193327(JP,A) 特開 昭63−182331(JP,A) 特開 昭63−178143(JP,A)Continuation of the front page (56) References JP-A-62-95289 (JP, A) JP-A-2-43022 (JP, A) JP-A-1-186380 (JP, A) JP-A-63-237989 (JP) JP-A-63-170018 (JP, A) JP-A-1-193327 (JP, A) JP-A-63-182331 (JP, A) JP-A-63-178143 (JP, A)
Claims (2)
し、該基材層の片面に熱転写インキ層が設けられた熱転
写用リボンにおいて、該二軸配向ポリエステルフィルム
の横方向の温度寸法変化曲線を測定したときに、該曲線
の勾配が負から正に変化する点が存在し、該点における
温度が200℃以上であり、かつ該点におけるフィルムの
原長に対する寸法変化率が−5〜+5%であることを特
徴とする熱転写用リボン。In a thermal transfer ribbon having a biaxially oriented polyester film as a base material layer and a heat transfer ink layer provided on one surface of the base material layer, a lateral temperature dimensional change curve of the biaxially oriented polyester film is obtained. When measured, there is a point where the slope of the curve changes from negative to positive, the temperature at the point is 200 ° C. or more, and the dimensional change rate of the original length of the film at the point is −5 to + 5%. A ribbon for thermal transfer, characterized in that:
2〜10μmであり、かつ縦方向のF−5値が11〜15kg/m
m2であることを特徴とする請求項1記載の熱転写用リボ
ン。2. The biaxially oriented polyester film has a thickness of 2 to 10 μm and an F-5 value in the longitudinal direction of 11 to 15 kg / m 2.
2. The thermal transfer ribbon according to claim 1, wherein the thermal transfer ribbon is m2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2149116A JP2581270B2 (en) | 1990-06-06 | 1990-06-06 | Thermal transfer ribbon |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2149116A JP2581270B2 (en) | 1990-06-06 | 1990-06-06 | Thermal transfer ribbon |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0441297A JPH0441297A (en) | 1992-02-12 |
JP2581270B2 true JP2581270B2 (en) | 1997-02-12 |
Family
ID=15468068
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2149116A Expired - Lifetime JP2581270B2 (en) | 1990-06-06 | 1990-06-06 | Thermal transfer ribbon |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2581270B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU1052299A (en) * | 1997-11-13 | 1999-06-07 | Teijin Limited | Readily bondable polyester film |
JPH11147377A (en) * | 1997-11-18 | 1999-06-02 | Teijin Ltd | Biaxially oriented polyester film for heat-sensitive transfer ribbon |
WO1999028133A1 (en) * | 1997-12-02 | 1999-06-10 | Mitsubishi Polyester Film Corporation | Biaxially oriented polyester film for thermal transfer |
EP1022152A4 (en) | 1998-07-24 | 2001-01-24 | Teijin Ltd | Thermal transfer ribbon and base film thereof |
WO2001030584A1 (en) * | 1999-10-22 | 2001-05-03 | Teijin Limited | Laminated base film for thermal transfer recording medium |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6295289A (en) * | 1985-10-23 | 1987-05-01 | Teijin Ltd | Thermal transfer recording film |
JP2629861B2 (en) * | 1988-08-03 | 1997-07-16 | 東レ株式会社 | Biaxially oriented polyethylene terephthalate film |
-
1990
- 1990-06-06 JP JP2149116A patent/JP2581270B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0441297A (en) | 1992-02-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4675233A (en) | Ink transfer material for printer | |
KR20010024241A (en) | Thermal transfer ribbon and base film thereof | |
JP2581270B2 (en) | Thermal transfer ribbon | |
KR950004335B1 (en) | Transfer material for printer and manufacturing method thereof | |
KR100730525B1 (en) | Laminated Base Film for Thermal Transfer Recording Media | |
JPH0434960B2 (en) | ||
JP3750828B2 (en) | Ribbon for thermal transfer | |
JPH0453716B2 (en) | ||
JP2002178400A (en) | Biaxially oriented polyester film | |
JP2955187B2 (en) | Manufacturing method of transfer material for printer | |
JP2000052418A (en) | Polyester film for thermal transfer ink ribbon and thermal transfer ink ribbon using the same | |
JP3094544B2 (en) | Laminated polyester film | |
JP2990695B2 (en) | Transfer material for printer | |
JP2566624B2 (en) | Thermal transfer film | |
JP2733974B2 (en) | Thermal transfer material for printer | |
JP3148782B2 (en) | Laminated polyester film | |
JP3010635B2 (en) | Polyester film for thermal transfer | |
JP2005238623A (en) | Biaxially oriented polyester film for sublimation type thermal transfer ribbon | |
JPH10264337A (en) | Thermal transfer ribbon and film therefor | |
JP2001071651A (en) | Melt type heat sensitive transferring polyester film | |
JPH08230340A (en) | Film for thermal transfer ribbon | |
JPH068656A (en) | Transfer material for printer | |
JP2002036736A (en) | Ribbon for thermal transfer | |
JP2000218949A (en) | Film for thermal transfer ribbon and thermal transfer ribbon | |
JP2001071649A (en) | Biaxially oriented polyester film for thermal transfer ribbon, and thermal transfer ribbon |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20071121 Year of fee payment: 11 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081121 Year of fee payment: 12 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081121 Year of fee payment: 12 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091121 Year of fee payment: 13 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091121 Year of fee payment: 13 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101121 Year of fee payment: 14 |
|
EXPY | Cancellation because of completion of term | ||
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101121 Year of fee payment: 14 |