JPH04173292A - Thermal transfer recording medium - Google Patents
Thermal transfer recording mediumInfo
- Publication number
- JPH04173292A JPH04173292A JP2298930A JP29893090A JPH04173292A JP H04173292 A JPH04173292 A JP H04173292A JP 2298930 A JP2298930 A JP 2298930A JP 29893090 A JP29893090 A JP 29893090A JP H04173292 A JPH04173292 A JP H04173292A
- Authority
- JP
- Japan
- Prior art keywords
- thermal transfer
- transfer layer
- layer
- base material
- diatomaceous earth
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000012546 transfer Methods 0.000 title claims abstract description 86
- 239000000843 powder Substances 0.000 claims abstract description 24
- 239000000463 material Substances 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 13
- 239000002689 soil Substances 0.000 claims description 3
- 239000010410 layer Substances 0.000 abstract description 59
- 239000005909 Kieselgur Substances 0.000 abstract description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 22
- 239000011347 resin Substances 0.000 abstract description 17
- 229920005989 resin Polymers 0.000 abstract description 17
- 239000002245 particle Substances 0.000 abstract description 11
- 238000000034 method Methods 0.000 abstract description 10
- 239000011241 protective layer Substances 0.000 abstract description 8
- 230000000694 effects Effects 0.000 abstract description 3
- 229920000298 Cellophane Polymers 0.000 abstract description 2
- 238000004873 anchoring Methods 0.000 abstract description 2
- 239000002985 plastic film Substances 0.000 abstract description 2
- 229920006255 plastic film Polymers 0.000 abstract description 2
- 238000004040 coloring Methods 0.000 abstract 1
- 239000002904 solvent Substances 0.000 description 10
- 238000007639 printing Methods 0.000 description 8
- 238000003860 storage Methods 0.000 description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 239000003086 colorant Substances 0.000 description 5
- 239000012943 hotmelt Substances 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000008542 thermal sensitivity Effects 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 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
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、ワープロ、ファクシミリ、バーコード等のサ
ーマルヘッドを用いた感熱転写記録装置に使用する感熱
転写記録媒体の改良に関する。更に詳しくは、平滑度の
低い紙へのカバーラ・ツブ性や、ドツトの再現性等の高
い熱感度性を保持しながら、高温、長期保存の際に熱転
写層の成分が基材の裏面に移行することを防11−シ、
保存安定性を良好にすることにより印字上、走行上のト
ラブルを防止した感熱転写記録媒体に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to improvement of a thermal transfer recording medium used in a thermal transfer recording device using a thermal head for word processors, facsimile machines, bar codes, etc. More specifically, while maintaining high thermal sensitivity such as coverage and flatness on paper with low smoothness and dot reproducibility, the components of the thermal transfer layer migrate to the back side of the base material during long-term storage at high temperatures. 11-shi,
This invention relates to a thermal transfer recording medium that prevents printing and running troubles by improving storage stability.
感熱転写記録方法は、装置が簡便で低騒音、小型、低価
格、かつ普通紙にも容易に記録可能なことから、広く普
及している。しかしながら、被転写紙の表面平滑性に印
字品質が影響されやすく、表面平滑性の劣る被転写紙に
対しては鮮明な印字を行うことは困難であった。Thermal transfer recording method is widely used because the device is simple, has low noise, is small, low cost, and can easily record on plain paper. However, the print quality is easily affected by the surface smoothness of the transfer paper, and it has been difficult to make clear prints on the transfer paper with poor surface smoothness.
また、近年のサーマルヘッドの高速化、高分解能化に伴
ってサーマルヘッドが蓄熱しやすくなっており、その結
果発熱部の周囲部も温度」二昇するので被転写紙に地汚
れが発生しやすい課題も生じている。In addition, as the speed and resolution of thermal heads have increased in recent years, it has become easier for thermal heads to accumulate heat, and as a result, the temperature of the surrounding area of the heat generating part also rises, making it easier for background stains to occur on the transfer paper. Challenges have also arisen.
上記課題を解決するために最近では、基材の一方の面(
以下裏面とする)にスティック防止を目的とした耐熱保
護層を設け、基材の他方の面(以下表面とする)の熱溶
融性インク層を積層構造とし、着色層である第1熱転写
層を設け、さらにその」二に低平滑紙への印字性向上・
接着性向」二・耐地汚れ性を1]的とした、スチレン樹
脂、アクリル樹脂、ポリアミド樹脂、ブチラール樹脂、
塩ビー酢ビ共重合樹脂、エチレン−酢ビ共重合樹脂等の
熱可塑性を主成分として、必要に応じて粘着付与剤樹脂
、ワックス、着色剤等を混合したものからなる第2熱転
写層を設ける構造が一般的である。Recently, in order to solve the above problems, one side of the base material (
A heat-resistant protective layer is provided on the back side (hereinafter referred to as the back side) for the purpose of preventing stickiness, a heat-melting ink layer on the other side of the base material (hereinafter referred to as the front side) has a laminated structure, and the first thermal transfer layer, which is a colored layer, is provided on the other side (hereinafter referred to as the front side) of the base material. Furthermore, the second feature is improved printing performance on low-smooth paper.
Styrene resin, acrylic resin, polyamide resin, butyral resin, with adhesion properties (2) and dirt resistance (1).
A second thermal transfer layer is provided, which is made of a thermoplastic material such as vinyl chloride-vinyl acetate copolymer resin or ethylene-vinyl acetate copolymer resin, mixed with tackifier resin, wax, colorant, etc. as necessary. The structure is common.
しかし、このような構造のリボンではロール状態での高
温保存や長期保存において、裏面の耐熱保護層へトップ
の熱転写層成分の移行が発生し、印字・走行上しばしば
トラブルか発生している。However, when ribbons with such a structure are stored at high temperatures or for long periods in a rolled state, components of the top thermal transfer layer migrate to the heat-resistant protective layer on the back side, which often causes problems in printing and running.
従来の感熱転写記録媒体の構造によれば、低平滑紙への
カバーラップ性、ドツトの再現性、耐地汚れ性という印
字性の面ではある程度解決されている。一方、高い熱感
度によるぐY明な印字を得るためには、第2熱転写層で
あるI・ツブ層の主成分としては軟化点か低い熱可塑性
樹脂を使用する必要が生じている。しかし第2熱転写層
であるトップ層に軟化点の低い樹脂を使用した場合、ロ
ールの状態で高温保存或いは長期保存すると、トップ層
の樹脂か直接接触している基材裏面又はこの裏面に設け
られている耐熱保護層側へ移行してしまい、カバーラッ
プ性の低下による低平滑紙への印字品位の低下、サーマ
ルヘッドのヘット旨9れによる印字品位の低下、スティ
ック現象の発生、カセット内でのリボンの走行上のトラ
ブルの発生等の課題か生じていた。According to the structure of conventional thermal transfer recording media, printing properties such as cover wrap properties on low-smooth paper, dot reproducibility, and background stain resistance have been solved to some extent. On the other hand, in order to obtain clear printing due to high thermal sensitivity, it is necessary to use a thermoplastic resin with a low softening point as the main component of the I/tub layer, which is the second thermal transfer layer. However, when a resin with a low softening point is used for the top layer, which is the second thermal transfer layer, if it is stored in a roll at high temperatures or for a long period of time, the resin of the top layer may be formed on the back of the base material that is in direct contact with it or on this back surface. The print quality on low-smooth paper decreases due to a decrease in cover wrap properties, the print quality decreases due to head misalignment of the thermal head, the stick phenomenon occurs, and the print quality in the cassette decreases. Problems such as problems with ribbon running occurred.
すなわち、従来の感熱転写記録媒体では高温及び長期保
存時の保存性と、低平滑紙へのカバーラップ性、ドツト
の再現性、耐地汚れ性といった印字性の面で両立できな
いという課題があった。In other words, conventional thermal transfer recording media had the problem of being unable to achieve both high-temperature and long-term storage stability, cover-wrap performance on low-smooth paper, dot reproducibility, and stain resistance. .
本発明の目的は従来の感熱転写記録媒体では得られなか
った、高温及び長期保存時に熱転写層の成分がJA利裏
面又はこの裏面に設けられている耐熱保護層へ移行する
ことを防止し、平滑性が劣る被転写紙への転写の鮮明性
、被転写紙の地汚れが大幅に改良された感熱転写記録媒
体を提Cj(することにある。The purpose of the present invention is to prevent the components of the thermal transfer layer from migrating to the JA back side or the heat-resistant protective layer provided on this back side during high temperature and long-term storage, which could not be achieved with conventional thermal transfer recording media. The purpose of this invention is to provide a thermal transfer recording medium that has greatly improved the clarity of transfer to transfer paper, which has poor properties, and the background smearing of the transfer paper.
本発明者らは前記課題を解決するために鋭意研究の結果
、第2熱転写層として特定の無機微粉末を含む配合組成
物を塗工することにより解決し得ることを見出し本発明
を完成した。As a result of intensive research to solve the above problem, the present inventors found that the problem could be solved by applying a blended composition containing a specific inorganic fine powder as the second thermal transfer layer, and completed the present invention.
すなわち、本発明の感熱転写記録媒体は、基拐」二に着
色層である第1熱転写層を設け、さらにその上に第2熱
転写層を設けてなる積層構造の感熱転写記録媒体におい
て、第2熱転写層としてけいそう土微粉末を含む配合組
成物を塗工してなることを特徴とする。That is, the thermal transfer recording medium of the present invention has a laminated structure in which a first thermal transfer layer, which is a colored layer, is provided on the substrate and a second thermal transfer layer is further provided thereon. It is characterized in that it is formed by coating a blended composition containing fine diatomaceous earth powder as a thermal transfer layer.
次に本発明の構成について説明する。Next, the configuration of the present invention will be explained.
28、Iとしては2〜2 Q lt mの厚さのポリエ
ステル、ポリカーボネート、ポリイミド等の比較的耐熱
性に優れるプラスチックフィルム、セロファン、紙等が
使用できる。必要に応じてサーマルヘッドと接する面に
シリコン変性ポリマー系、フッ素系ポリマー等からなる
耐熱保護層やスティック防11−層を設けてもよい。As 28, I, a plastic film having relatively excellent heat resistance such as polyester, polycarbonate, polyimide, etc. having a thickness of 2 to 2 Qltm, cellophane, paper, etc. can be used. If necessary, a heat-resistant protective layer or an anti-stick layer made of a silicone-modified polymer, a fluorine-based polymer, or the like may be provided on the surface in contact with the thermal head.
第1熱転写層は着色剤、ビヒクル及び各種添加−5=
剤か加わった熱溶融性インクからなる。着色剤としては
カーボンブラック、有機顔料、染r1等を単独又は複数
使用することができる。好ましくは十分な着色濃度を有
し、光、熱、温湿度、溶剤等により変退色しないものを
選定すると良い。ビヒクルとしては融点が45〜] 2
0 ’Cのワックスが主成分であり、パラフィンワック
ス、カルナバワックス、マイクロクリスタリンワックス
、キャンデリラワックス、ポリエチレンワックス、木蝋
、蜜蝋、脂肪酸アミド、脂肪酸エステル等゛がらjx定
される一種又は二種以上を用いるが、本発明では格別に
は限定しない。熱溶融性インクには上記の着色剤ビヒク
ル以外に、必要に応して熱可塑性樹脂からなる固着剤、
分散剤、レベリング剤等の各種添加剤を加えてもよい。The first thermal transfer layer consists of a hot melt ink with a colorant, a vehicle, and various additives. As the coloring agent, carbon black, organic pigment, dye R1, etc. can be used alone or in combination. It is preferable to select a material that has sufficient color density and does not discolor or fade due to light, heat, temperature/humidity, solvents, etc. As a vehicle, the melting point is 45 ~] 2
0 'C wax is the main component, and one or more types specified by paraffin wax, carnauba wax, microcrystalline wax, candelilla wax, polyethylene wax, wood wax, beeswax, fatty acid amide, fatty acid ester, etc. However, the present invention does not particularly limit it. In addition to the above-mentioned colorant vehicle, the hot-melt ink may contain a fixing agent made of a thermoplastic resin, if necessary.
Various additives such as dispersants and leveling agents may be added.
第]熱転写層の組成及び厚さは必要な印字濃度と熱感度
によって決定されるか、厚さは0.1〜1.0 (t
、好ましくは2〜5μである。The composition and thickness of the thermal transfer layer are determined by the required printing density and thermal sensitivity, and the thickness is 0.1 to 1.0 (t
, preferably 2 to 5μ.
第2熱転写層は、けいそう土微粉末を含む配合組成物を
塗工してなる。厚みは0.05〜5. 0μm1好まし
くは0,1〜2,0μmである。また、必要に応じて基
材と第1熱転写層の間に剥離層または接着層を設けても
よい。該配合組成物は、熱可塑性樹脂を主成分とし、け
いそう土微粉末、揮発性溶剤からなり、必要に応じて、
軟化点調整剤、ワックス、着色剤、界面活性剤、レベリ
ング剤などの添加剤を加えてもよい。The second thermal transfer layer is formed by coating a blended composition containing fine diatomaceous earth powder. The thickness is 0.05~5. 0 μm, preferably 0.1 to 2.0 μm. Furthermore, a release layer or an adhesive layer may be provided between the base material and the first thermal transfer layer, if necessary. The blended composition contains a thermoplastic resin as a main component, diatomaceous earth fine powder, and a volatile solvent, and if necessary,
Additives such as softening point regulators, waxes, colorants, surfactants, and leveling agents may also be added.
主成分とする熱可塑性樹脂はスチレン樹脂、アクリル樹
脂、ポリアミド樹脂、ブチラール樹脂、塩ビー酢ビ共重
合樹脂、エチレン−酢ビ共重合樹脂等の、軟化点が50
〜200℃、好ましくは、70〜1−50℃の熱可塑性
樹脂の一種又は二種以上を用いる。けいそう土微粉末を
均一に混合するため、また配合組成物を第1熱転写層上
に薄膜状に容易に塗工するために、配合する樹脂類は揮
発性溶剤に溶解するものを選定するのが好ましい。The main component thermoplastic resins are styrene resins, acrylic resins, polyamide resins, butyral resins, vinyl chloride-vinyl acetate copolymer resins, ethylene-vinyl acetate copolymer resins, etc., and have a softening point of 50.
-200°C, preferably 70-1-50°C, one or more thermoplastic resins are used. In order to uniformly mix the diatomaceous earth fine powder and to easily coat the blended composition in a thin film form on the first thermal transfer layer, the resins to be blended should be selected to be soluble in volatile solvents. is preferred.
揮発性溶剤としては、アルコール類、ケトン類、エステ
ル類をあげることができる。溶剤の使用量は、使用した
樹脂とけいそう土の粒子径とそれらの混合比、溶剤の種
類、塗工方式、第2熱転写層の厚みにもよるが、50〜
99.5重量%がよい。Examples of volatile solvents include alcohols, ketones, and esters. The amount of solvent used depends on the particle size of the resin and diatomaceous earth used, their mixing ratio, the type of solvent, the coating method, and the thickness of the second thermal transfer layer, but it is between 50 and 50 ml.
99.5% by weight is good.
軟化点調整剤としては、粘着(=I与剤樹脂等に代表さ
れる低−中分子の樹脂、具体的にはケトン樹脂などをあ
げることができる。Examples of the softening point adjusting agent include low-to-medium molecular weight resins such as adhesive resins, specifically ketone resins.
第2熱転写層すなわち、配合組成物の必須成分であるけ
いそう土としては、通常に産出されるけいそう殻質及び
/又はけいそう殻以外のケイ酸殻質殻からできているも
のの一種又は二種以上を用いることができる。一般にけ
いそう土は1〜120μmの範囲の粒子径のものが原土
として得られるが、本発明ではこれを粉砕及び/又は分
級して平均粒子径が0.5〜10μmの範囲内の微粉末
を用いる。平均粒子径が0.5μm未満では保存性は改
良されず、]、 Otlmを超えると印字性が劣化する
。第2熱転写層に含有されるけいそう土微粉末の比率は
0.5〜25重量%がよく、粒子径と同様に0.5重量
%未満では保存性は改良されず、25重量%を超えると
印字性が劣化する。The diatomaceous earth that is an essential component of the second thermal transfer layer, that is, the blended composition, is one or two types of diatomaceous earth made of normally produced diatomaceous earth and/or silicic acid earth other than diatomaceous earth. More than one species can be used. Generally, diatomaceous earth is obtained as raw soil with a particle size in the range of 1 to 120 μm, but in the present invention, this is pulverized and/or classified to form a fine powder with an average particle size in the range of 0.5 to 10 μm. Use. If the average particle diameter is less than 0.5 μm, the storage stability will not be improved, and if it exceeds Otlm, the printing performance will deteriorate. The ratio of the diatomaceous earth fine powder contained in the second thermal transfer layer is preferably 0.5 to 25% by weight; similarly to the particle size, if it is less than 0.5% by weight, the storage stability will not be improved, and if it exceeds 25% by weight. and printability deteriorates.
第2転写層に塗工される配合組成物の調製方法は、熱可
塑性樹脂を溶解する単一または混合溶剤を用いて、熱可
塑性樹脂、けいそう土微粉末、必要に応じて前記添加剤
を加えて、混合攪拌する方法、前記配合物をロールミル
、ニーダ−などの混練機を用いて混練した後、混線物を
溶剤でレットダウンする方法などがあるが、基本的には
熱可塑性樹脂を溶剤に完全に溶解し、けいそう土微粉末
を均一に混合することか重要である。The method for preparing the blended composition to be applied to the second transfer layer involves using a single or mixed solvent that dissolves the thermoplastic resin, and adding the thermoplastic resin, diatomaceous earth fine powder, and, if necessary, the additives. In addition, there are methods of mixing and stirring, methods of kneading the above-mentioned mixture using a kneading machine such as a roll mill or kneader, and then letting down the mixed material with a solvent, but basically the thermoplastic resin is mixed with a solvent. It is important to completely dissolve the diatomaceous earth powder and mix it uniformly.
第1熱転写層および第2熱転写層の形成方法は、基材ま
たは必要に応じて裏面に耐熱保護層を設けた基材の表面
に第1熱転写層の熱溶融性インクをホットメルト法もし
くは溶剤法て塗布し第1熱転写層を形成し、その上に配
合組成物をグラビアロール法、キスロール法、タイヤバ
ー法などの公知の方法で塗工してのち、溶剤を揮発させ
て第2熱転写層を得る。The method for forming the first thermal transfer layer and the second thermal transfer layer is to apply the heat-melt ink of the first thermal transfer layer to the surface of the base material or a base material provided with a heat-resistant protective layer on the back side as necessary by a hot-melt method or a solvent method. A first thermal transfer layer is formed by applying the compounded composition thereon by a known method such as a gravure roll method, a kiss roll method, or a tire bar method, and then the solvent is evaporated to form a second thermal transfer layer. obtain.
〔作 用〕 ・
本発明の感熱転写記録媒体の第2転写層に含有するけい
そう土微粉末はつぎの作用を有する。[Function] - The fine diatomaceous earth powder contained in the second transfer layer of the thermal transfer recording medium of the present invention has the following function.
第2熱転写層にけいそう土微粉末を含有させる一9=
ことは、パンケーキの状態で基本的に基材の表面と第2
熱転写層の熱可塑性樹脂の表面とを可能な限り接触させ
ないことで保存性を向上させることにある。そのために
は第2熱転写層表面において、けいそう土微粉末が部分
的に露出している。また基材の裏面との擦れやカセット
内での走行時においてもげいそう土微粉末が脱落するこ
とのないように第2熱転写層内部に強く固着されている
。Incorporating fine diatomaceous earth powder into the second thermal transfer layer 9 = This means that the surface of the base material and the second
The purpose is to improve storage stability by minimizing contact between the surface of the thermoplastic resin of the thermal transfer layer and the surface of the thermoplastic resin. For this purpose, the diatomaceous earth fine powder is partially exposed on the surface of the second thermal transfer layer. Further, the fine soil powder is strongly fixed inside the second thermal transfer layer so that it will not fall off when it rubs against the back surface of the base material or when it travels within the cassette.
一方けいそう土はその成因からも明らかなように、多種
多様の複雑な粒子形状を有しながら、内部に多数の空孔
を有している粒子である。これを粉砕及び/又は分級し
て平均粒子径が0.5〜10μmの範囲の微粉末を用い
ることにより、第2熱転写層の表面から適当な状態に露
出して基材の裏面と第2熱転写層の熱可塑性樹脂表面と
の直接接触を防止し、空孔に樹脂が入りこんで大きなア
ンカー効果が得られる。On the other hand, as is clear from its origin, diatomaceous earth is a particle that has a wide variety of complex particle shapes and has a large number of pores inside. By pulverizing and/or classifying this powder and using a fine powder with an average particle size in the range of 0.5 to 10 μm, it is exposed in an appropriate state from the surface of the second thermal transfer layer and transferred to the back surface of the base material and the second thermal transfer layer. Direct contact with the thermoplastic resin surface of the layer is prevented, and the resin enters the pores, creating a large anchoring effect.
また、上記したけいそう土微粉末が露出した第2熱転写
層表面が形成されれば、必然的にその表面は粗面化する
ことによって摩擦係数が大きくなる。特にシリアルプリ
ンター用の感熱転写記録媒体の走行が基材の裏面との摩
擦係数との差によって生じることから摩擦係数の大きい
ことは好ましいことになり、ヘッド周辺での耐スティッ
ク性、耐蛇行性等も改良される。Furthermore, if the surface of the second thermal transfer layer is formed with the above-mentioned diatomaceous earth fine powder exposed, the surface will inevitably become rough and the coefficient of friction will increase. In particular, since the running of thermal transfer recording media for serial printers is caused by the difference in the coefficient of friction between the back surface of the base material and the back surface of the substrate, a large coefficient of friction is desirable, and it is desirable to have a high coefficient of friction, such as stick resistance and meandering resistance around the head. will also be improved.
[実施例]
以下、実施例を挙げて本発明を更に具体的に説明するか
、本発明はこの実施例によって限定されるものではない
。[Examples] Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited by these Examples.
実施例1 熱溶融性インキの調製。Example 1 Preparation of hot melt ink.
エチレン−酢ビ共重合樹脂15重量%、カーボンブラッ
ク20重量96、カルナバワックス20重量%およびパ
ラフィンワックス45重量%を加熱したインク用三木ロ
ールを用いて十分に混練して熱溶融性インクを調製した
。A hot-melt ink was prepared by sufficiently kneading 15% by weight of ethylene-vinyl acetate copolymer resin, 20% by weight of carbon black, 20% by weight of carnauba wax, and 45% by weight of paraffin wax using a heated Miki roll for ink. .
配合組成物の調製。Preparation of formulated compositions.
ポリビニルブチラール50重量部、軟化点調整剤として
のケトン樹脂25重量部および平均粒子径が3μmのけ
いそう土微粉末15重量部を酢酸エチル中に投入して十
分に撹拌し、濃度10重量%の塗工用酢酸エチル溶液と
し配合組成物を調製した。50 parts by weight of polyvinyl butyral, 25 parts by weight of ketone resin as a softening point regulator, and 15 parts by weight of diatomaceous earth fine powder with an average particle size of 3 μm were added to ethyl acetate and thoroughly stirred to obtain a concentration of 10% by weight. A blended composition was prepared as an ethyl acetate solution for coating.
感熱転写記録媒体の作製・
裏面にンリコン変性ウレタン樹脂からなる耐熱保護層が
設けられた4 0μm厚のポリエステルフィルムの表面
に、」二記の熱溶融性インクをポットメルトグラビアロ
ール
工し、第1熱転写層を形成した。つぎにこの第]熱転写
層の上に上記配合組成物をワイヤバーにて塗工して、乾
燥し、厚さl lt mの第2熱転写層を形成して、本
発明の感熱転写記録媒体を得た。Preparation of heat-sensitive transfer recording medium: The heat-melt ink described in "2" was applied with a pot-melt gravure roll onto the surface of a 40 μm thick polyester film, the back surface of which was provided with a heat-resistant protective layer made of urethane-modified resin. A thermal transfer layer was formed. Next, the above-mentioned blended composition is applied onto the thermal transfer layer using a wire bar and dried to form a second thermal transfer layer having a thickness of l lt m to obtain the thermal transfer recording medium of the present invention. Ta.
比較例]
第2熱転写層の配合組成物のけいそう生機粉末を除いた
他は、実施例1と同様にして感熱転写記録媒体を得た。Comparative Example] A thermal transfer recording medium was obtained in the same manner as in Example 1, except that the diatomaceous greige powder in the composition of the second thermal transfer layer was omitted.
比較例2
第2熱転写層の配合組成物のうち、けいそう生機粉末を
、平均粒子径は3μmと同じくして、無孔質で形状か鱗
片状に揃っているタルク微粉末に替えた他は、゛実施例
]と同様にして感熱転写記録媒体を得た。Comparative Example 2 In the composition of the second thermal transfer layer, the diatomaceous greige powder was replaced with fine talc powder, which had the same average particle size of 3 μm and was non-porous and uniform in shape and scale. A thermal transfer recording medium was obtained in the same manner as in Example.
次に上記の操作で得られた感熱転写記録媒体をロール状
に巻取り、6 0 ’C − 2 4時間保存した後の
耐熱保護層側への第2熱転写層の成分の移行度合の顕微
鏡観察、第2熱転写層表面の摩擦係数の測定(JIS
P−81.47紙の摩擦試験法に準拠、対象物は三菱鉛
筆■製ユニワープロ用紙)、市販の感熱転写型プリンタ
ーを用いてベック平滑度50秒の被転写紙に印字試験を
行った。その結果を下表に示す。Next, the thermal transfer recording medium obtained by the above operation was wound up into a roll and stored at 60'C-2 for 4 hours, after which the degree of migration of the components of the second thermal transfer layer to the heat-resistant protective layer side was observed using a microscope. , Measurement of the coefficient of friction on the surface of the second thermal transfer layer (JIS
A printing test was conducted on transfer paper with a Beck smoothness of 50 seconds using a commercially available thermal transfer printer based on the P-81.47 paper friction test method (Uni word processor paper manufactured by Mitsubishi Pencil ■). The results are shown in the table below.
本発明の感熱転写記録媒体は実施例、比較例の試験結果
でも明らかなように、従来の感熱転写記録媒体と比較し
て、高温及び長期保存時の熱転写層の成分の基材裏面又
は耐熱保護層への移行を防止し、平滑性が劣る被転写紙
への転写の鮮明性、被転写紙の地汚れ妻大幅に改良した
優れた積層構造の感熱転写記録媒体である。As is clear from the test results of Examples and Comparative Examples, the thermal transfer recording medium of the present invention is more effective in protecting the back side of the base material and heat-resistant components of the thermal transfer layer during high-temperature and long-term storage than conventional thermal transfer recording media. This is a heat-sensitive transfer recording medium with an excellent laminated structure that prevents transfer to layers, greatly improves the clarity of transfer to transfer paper with poor smoothness, and greatly improves the background stains on transfer paper.
Claims (1)
上に熱可塑性樹脂を主成分とする第2熱転写層を設けて
なる積層構造の感熱転写記録媒体において、第2熱転写
層がけいそう土微粉末を含む配合組成物を塗工してなる
ことを特徴とする感熱転写記録媒体。In a thermal transfer recording medium having a laminated structure in which a first thermal transfer layer, which is a colored layer, is provided on a base material, and a second thermal transfer layer containing a thermoplastic resin as a main component is further provided thereon, the second thermal transfer layer is A heat-sensitive transfer recording medium characterized in that it is coated with a blended composition containing fine soil powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2298930A JPH04173292A (en) | 1990-11-06 | 1990-11-06 | Thermal transfer recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2298930A JPH04173292A (en) | 1990-11-06 | 1990-11-06 | Thermal transfer recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04173292A true JPH04173292A (en) | 1992-06-19 |
Family
ID=17866026
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2298930A Pending JPH04173292A (en) | 1990-11-06 | 1990-11-06 | Thermal transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04173292A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2019171712A (en) * | 2018-03-29 | 2019-10-10 | シヤチハタ株式会社 | ink ribbon |
-
1990
- 1990-11-06 JP JP2298930A patent/JPH04173292A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2019171712A (en) * | 2018-03-29 | 2019-10-10 | シヤチハタ株式会社 | ink ribbon |
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