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JP2579685B2 - Thermal transfer material - Google Patents
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JP2579685B2 - Thermal transfer material - Google Patents

Thermal transfer material

Info

Publication number
JP2579685B2
JP2579685B2 JP1168404A JP16840489A JP2579685B2 JP 2579685 B2 JP2579685 B2 JP 2579685B2 JP 1168404 A JP1168404 A JP 1168404A JP 16840489 A JP16840489 A JP 16840489A JP 2579685 B2 JP2579685 B2 JP 2579685B2
Authority
JP
Japan
Prior art keywords
layer
heat
transfer material
thermal transfer
infrared absorbing
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 - Fee Related
Application number
JP1168404A
Other languages
Japanese (ja)
Other versions
JPH0334893A (en
Inventor
真木子 池内
幸史 花田
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.)
Artience Co Ltd
Original Assignee
Toyo Ink Mfg Co 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 Toyo Ink Mfg Co Ltd filed Critical Toyo Ink Mfg Co Ltd
Priority to JP1168404A priority Critical patent/JP2579685B2/en
Publication of JPH0334893A publication Critical patent/JPH0334893A/en
Application granted granted Critical
Publication of JP2579685B2 publication Critical patent/JP2579685B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • B41M5/382Contact thermal transfer or sublimation processes
    • B41M5/385Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • 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
    • B41M5/46Thermography ; 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 characterised by the light-to-heat converting means; characterised by the heat or radiation filtering or absorbing means or layers
    • 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
    • B41M5/46Thermography ; 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 characterised by the light-to-heat converting means; characterised by the heat or radiation filtering or absorbing means or layers
    • B41M5/465Infrared radiation-absorbing materials, e.g. dyes, metals, silicates, C black

Landscapes

  • Thermal Transfer Or Thermal Recording In General (AREA)

Description

【発明の詳細な説明】 〔発明の目的〕 (産業上の利用分野) 本発明は,特定の近赤外線を選択的に吸収する近赤外
線吸収剤を含む層を有する,耐光性に優れた,ほぼ無色
あるいはカラーの感熱転写材に関する。さらに詳細に
は,紫外線による近赤外線吸収効果の低下を抑えた,近
赤外線吸収剤を含む層を有する感熱転写材を用いて感熱
転写記録することにより耐光性に優れ,製品イメージに
合う,または目立たないバーコード等を与える感熱転写
材に関する。
DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Industrial application field) The present invention provides a light-resistant, almost light-resistant, It relates to a colorless or color thermal transfer material. More specifically, thermal transfer recording using a thermal transfer material having a layer containing a near-infrared absorbing agent, which suppresses the near-infrared absorbing effect due to ultraviolet light, has excellent light resistance and is suitable for product images or stands out. The present invention relates to a thermal transfer material which gives no bar code or the like.

(従来の技術) 従来,ファクトリーオートメーション,POS,流通にお
いて製品管理の合理化を図る為に製品にバーコードが付
与されているが,黒以外の色の色材のほとんどはバーコ
ードリーダーの検出波長域に充分な吸収を持っていない
為,色の選択範囲が限定される。その為,製品イメージ
に合わせて任意に色調のバーコードを付与することがで
きず,製品の美観を損なうものであった。
(Prior art) Conventionally, barcodes are assigned to products in order to streamline product management in factory automation, POS, and distribution, but most of the color materials other than black are in the detection wavelength range of the barcode reader. Does not have sufficient absorption to limit the range of color choices. For this reason, it is not possible to arbitrarily add a color tone barcode in accordance with the product image, which impairs the aesthetic appearance of the product.

特開昭64−30788号公報でカーボンブラックを除く近
赤外線吸収剤を熱溶融性インキ層に添加する方法が提案
されているが,バーコードの例では耐光性が劣り,太陽
光に曝すと充分な吸収効果が得られなくなった。また,
単純に隠蔽性の高い色剤と混合した場合,近赤外線吸収
の効果が充分発揮されないという欠点があった。
JP-A-64-30788 proposes a method of adding a near-infrared absorbing agent other than carbon black to a hot-melt ink layer. However, in the case of a bar code, the light resistance is poor, and it is sufficient when exposed to sunlight. No significant absorption effect. Also,
When simply mixed with a colorant having a high hiding property, there is a disadvantage that the effect of near-infrared absorption is not sufficiently exhibited.

また,ベースフィルムの表面に単に熱溶融性インキ層
を設けたものを用いて感熱転写記録することにより得ら
れる転写物表面は,平滑なベースフィルムと熱溶融性イ
ンキとの界面で剥離する為,平滑性が高く,光沢のある
表面になってしまう。しかし,光沢を有する面は一般に
角度によっては読取りが難しく,無光沢な印字表面が望
まれている。
In addition, the transfer surface obtained by thermal transfer recording using only a base film having a hot-melt ink layer provided thereon is peeled off at the interface between the smooth base film and the hot-melt ink. High smoothness and glossy surface. However, a glossy surface is generally difficult to read depending on the angle, and a matte printing surface is desired.

(発明が解決しようとする課題) 本発明者等は,黒以外のバーコードを作成する方法に
ついて鋭意検討した結果,耐光性,美観に優れ,製品イ
メージを損なわないほぼ無色またはカラーのバーコード
用等の感熱転写材を提供するものである。
(Problems to be Solved by the Invention) As a result of intensive studies on a method of producing a bar code other than black, the present inventors have found that a colorless or color bar code having excellent light resistance and aesthetic appearance, and which does not impair the product image. And the like.

〔発明の構成〕[Configuration of the invention]

(課題を解決するための手段) すなわち,本発明は、基材に、熱転写時に凝集破壊を
起こす層、紫外線吸収剤を含む熱溶融性インキ層および
690〜1000nmに吸収極大波長を有する、カーボンブラッ
ク以外の近赤外線吸収剤を含む熱溶融性インキ層を順次
設けてなることを特徴とする黒以外のバーコード用感熱
転写材に関する。
(Means for Solving the Problems) That is, the present invention relates to a base material, a layer which causes cohesive failure during thermal transfer, a hot-melt ink layer containing an ultraviolet absorbent, and
The present invention relates to a thermal transfer material for barcodes other than black, which is provided with a heat-meltable ink layer containing a near-infrared absorbing agent other than carbon black having an absorption maximum wavelength in the range of 690 to 1000 nm.

本発明の感熱転写材は、紫外線吸収剤を含む層を有し
ているので、本発明の感熱転写材を用いてサーマルヘッ
ドにより記録した場合には、耐光性に優れ、製品のイメ
ージに合うほぼ無色またはカラーの黒以外のバーコード
記録物を得ることができる。上記バーコード記録物は、
近赤外線を吸収検出する通常のバーコードリーダーによ
って読み取ることができ、各種製品の製品管理のために
付与される製造ロット番号や品番などの照合に有効であ
る。
Since the heat-sensitive transfer material of the present invention has a layer containing an ultraviolet absorbent, when recorded by a thermal head using the heat-sensitive transfer material of the present invention, the heat-sensitive transfer material is excellent in light resistance and almost matches the image of the product. Colorless or colored bar code recordings other than black can be obtained. The above barcode record is
It can be read by a normal bar code reader that absorbs and detects near infrared rays, and is effective for collation of manufacturing lot numbers and product numbers given for product management of various products.

本発明の紫外線吸収剤は,290〜400nmの有害な紫外線
を吸収する作用を持つもので,たとえば表1の化合物を
挙げることができる。上記紫外線吸収剤を含む層を熱転
写時に凝集破壊を起こす層と近赤外線吸収剤を含む層と
の間に設けて紫外線対策を施すことにより,記録物中の
近赤外線吸収剤の劣化を防ぎ,紫外線による近赤外線吸
収効果の低下を抑えることができる。また紫外線吸収層
中に抗酸化剤を併用することによりさらに効果を高めて
もよい。
The ultraviolet absorbent of the present invention has a function of absorbing harmful ultraviolet light having a wavelength of 290 to 400 nm, and examples thereof include the compounds shown in Table 1. By providing the above-mentioned layer containing the ultraviolet absorber between the layer causing cohesive failure during thermal transfer and the layer containing the near-infrared absorber and taking measures against ultraviolet rays, deterioration of the near-infrared absorber in the recorded matter is prevented, and , A decrease in the near-infrared absorption effect due to the above. The effect may be further enhanced by using an antioxidant in the ultraviolet absorbing layer.

近赤外線吸収剤を含む層の上には,カラー化のために
カーボンブラック以外の任意の色材を含む熱溶融性着色
インキ層を設けることができる。上記着色層中に使用可
能な色材は,赤,緑,青,黄,紅,藍の染・顔料,パス
テル・白・パール顔料,螢光染料,金・銀色の金属粉末
等であり,特に制限を受けるものではない。
On the layer containing the near-infrared absorbing agent, a hot-melt colored ink layer containing an arbitrary coloring material other than carbon black can be provided for coloring. Coloring materials that can be used in the coloring layer include red, green, blue, yellow, red, indigo dyes / pigments, pastel / white / pearl pigments, fluorescent dyes, and gold / silver metal powders. There is no restriction.

なお,場合によっては近赤外線吸収剤を含む層にカー
ボンブラック以外の着色剤を添加することも可能である
が,その場合,近赤外線の波長領域において隠蔽性の低
い色材を使うことが望ましい。例えば金属粉末のように
近赤外線の波長領域において隠蔽性の高い色材を使用す
る場合には近赤外線吸収剤と色材の層を分けたほうがよ
い。
In some cases, a coloring agent other than carbon black may be added to the layer containing the near-infrared absorbing agent. In this case, however, it is desirable to use a coloring material having a low concealing property in the near-infrared wavelength region. For example, when a coloring material having a high concealing property in a near infrared wavelength region such as a metal powder is used, it is better to separate layers of the near infrared absorbing agent and the coloring material.

本発明の近赤外線吸収剤とは通常690〜1000nm範囲の
電磁波を吸収するもので,例えば表2の化学構造式の化
合物やジチオール金属錯塩系,アントラキノン系,メル
カプトナフトール金属錯塩系,ナフトキノン系,シアニ
ン色素系等を挙げることができる。
The near-infrared absorbing agent of the present invention generally absorbs an electromagnetic wave in the range of 690 to 1000 nm. Dyes and the like can be mentioned.

ただし,用途によっては,異なる波長の近赤外線吸収
剤が用いられるために,1種または2種以上の近赤外線吸
収剤を使用することが好ましい。
However, it is preferable to use one or two or more kinds of near-infrared absorbing agents because near-infrared absorbing agents having different wavelengths are used depending on the application.

熱転写時に凝集破壊を起こす層は、熱溶融性インキ層
の転写・剥離時に凝集破壊を起こし、その破壊表面に凹
凸により、バーコード記録物に艶消し効果を与え、バー
コードリーダーによる読み取りを容易にする。なお、凝
集破壊を起こす層には、通常は着色剤を含まない。凝集
破壊性層に含有される化合物としては,例えば高級脂肪
酸アミドもしくはその誘導体がある。なお,凝集破壊性
層については,特願昭62−60215号明細書に開示してあ
る。
The layer that causes cohesive failure during thermal transfer causes cohesive failure when transferring and peeling off the hot-melt ink layer, and its uneven surface gives the matte effect to the barcode record, making it easy to read with a barcode reader. I do. The layer that causes cohesive failure usually does not contain a coloring agent. Examples of the compound contained in the cohesive failure layer include a higher fatty acid amide or a derivative thereof. The cohesive failure layer is disclosed in Japanese Patent Application No. 62-60215.

本発明の紫外線吸収層,近赤外線吸収層,着色層およ
び凝集破壊層を基材上に設けるためにはホットメルトコ
ーティング法あるいは,より好ましくは上記化合物を媒
体中に分散した塗液をソルベントコーティングする方法
がある。紫外線吸収層,近赤外線吸収層および凝集破壊
層の塗布厚は,それぞれ0.1μm及至2μmが適当であ
る。着色層の塗布厚は0.5ないし10μmが適当である。
塗布厚が薄すぎると各層の効果が少なくなり,厚すぎる
と総塗布厚が大きくなり,転写材をロール巻きにしたと
き,巻き太りを起こしたり,エネルギー感度が低下して
しまう。
In order to provide the ultraviolet-absorbing layer, near-infrared-absorbing layer, coloring layer and cohesive failure layer of the present invention on a substrate, a hot melt coating method or, more preferably, solvent coating of a coating liquid in which the above compound is dispersed in a medium. There is a way. The coating thickness of the ultraviolet absorbing layer, the near infrared absorbing layer and the cohesive failure layer is suitably 0.1 μm to 2 μm, respectively. The coating thickness of the colored layer is suitably 0.5 to 10 μm.
If the coating thickness is too thin, the effect of each layer will be reduced, and if it is too thick, the total coating thickness will be large, and when the transfer material is rolled, the winding will be thickened and the energy sensitivity will be reduced.

本発明の支持体には,従来公知のベースフィルムを用
いることができる。例えばポリエステルフィルム(ポリ
エチレンテレフタレート,ポリエチレンナフタレート
等),ポリアミドフィルム(ナイロン等),ポリオレフ
ィンフィルム(ポリプロピレン等),セルロース系フィ
ルム(トリアセテート等),ポリカーボネートフィルム
等がある。ポリエステルフィルムは,耐熱性,機械強
度,引張強度,引張安定性などが優れ最も好ましい。こ
の基材は薄いほど熱伝導性がよいが強度やインキ層の塗
工のし易さから3〜50μが最も好ましい。また,基材の
熱溶融性インキ層の反対面に耐熱性の樹脂からなるバッ
クコート層を設けてもよい。
A conventionally known base film can be used for the support of the present invention. For example, there are polyester films (polyethylene terephthalate, polyethylene naphthalate, etc.), polyamide films (nylon, etc.), polyolefin films (polypropylene, etc.), cellulose films (triacetate, etc.), polycarbonate films and the like. The polyester film is most preferable because of its excellent heat resistance, mechanical strength, tensile strength, tensile stability and the like. The thinner this substrate is, the better the thermal conductivity is, but the thickness is most preferably 3 to 50 μm from the viewpoint of strength and ease of coating the ink layer. Further, a back coat layer made of a heat-resistant resin may be provided on the surface of the substrate opposite to the heat-meltable ink layer.

本発明の熱溶融性インキ層には,従来公知の組成に使
用されている成分をそのまま用いることができる。かか
る成分の一例としては,ワックスおよび熱可塑性樹脂等
であり,これらをバインダーとして上記した染料や顔料
等によって着色したものなどが挙げられる。ワックスと
しては,キャンデリラワックス,カルナバワックス,ラ
イスワックス,木ろう,ホホバ油などの植物系ワック
ス,みつろう,ラノリン,鯨ろうなどの動物系ワック
ス,モンタンワックス,ペトロラタムなどの石油ワック
ス,合成ワックスとしてはフッシャートロピッシュワッ
クス,ポリエチレンワックスなどの合成炭化水素,モン
タンワックス誘導体などの変性ワックス,硬化ひまし
油,硬化ひまし油誘導体などの水素化ワックス,ラウリ
ン酸,パルミチン酸,ミリスチン酸,ステアリン酸,12
ヒドロキシステアリン酸などの脂肪酸,および脂肪酸ア
ミド,脂肪酸アニリド,イミドロウなどのワックス類,
樹脂としては,アクリル系,スチレン系,ロジン系,ビ
ニル系,アセタール系,ゴム系が好ましい。
In the hot-melt ink layer of the present invention, the components used in conventionally known compositions can be used as they are. Examples of such components include waxes and thermoplastic resins, which are colored with the above-described dyes and pigments as binders. Examples of waxes include candelilla wax, carnauba wax, rice wax, vegetable waxes such as wood wax and jojoba oil, animal waxes such as beeswax, lanolin, and spermaceti, petroleum waxes such as montan wax and petrolatum, and synthetic waxes. Synthetic hydrocarbons such as fusher tropic wax and polyethylene wax, modified waxes such as montan wax derivatives, hydrogenated waxes such as hardened castor oil and hardened castor oil derivatives, lauric acid, palmitic acid, myristic acid, stearic acid, 12
Fatty acids such as hydroxystearic acid, and waxes such as fatty acid amides, fatty acid anilides and imido wax;
As the resin, acrylic, styrene, rosin, vinyl, acetal, and rubber are preferable.

上記熱溶融性インキには必要に応じて,少量の可塑
剤,分散剤,活性剤,帯電防止剤,安定剤等の添加剤を
混ぜることができる。
If necessary, a small amount of additives such as a plasticizer, a dispersant, an activator, an antistatic agent, and a stabilizer can be added to the hot-melt ink.

(実施例) 以下,実施例によって本発明を詳細に説明する。実施
例中の部は,すべて「重量部」を表す。
Hereinafter, the present invention will be described in detail with reference to examples. All parts in the examples represent "parts by weight".

実施例1 下記組成の塗液をアトライターにて常温で分散混合
し,凝集破壊層形成用インキを得た。得られたインキを
6μmのポリエチレンテレフタレートフィルム上にグラ
ビアコート法にて塗布厚1μmに塗布した。
Example 1 A coating liquid having the following composition was dispersed and mixed at room temperature using an attritor to obtain an ink for forming a cohesive failure layer. The obtained ink was applied on a 6 μm polyethylene terephthalate film by a gravure coating method to a coating thickness of 1 μm.

ステアリン酸リチウム(融点216℃) 1部 カルナバワックス 19部 エバフレックス420 1部 (三井ポリケミカル(株)製) トルエン 79部 ついで、下記組成の塗液をアトライターにて常温で充
分に分散し、得られた紫外線吸収インキを上記凝集破壊
層の上にグラビアコート法にて塗布厚1μmに塗布し
た。
Lithium stearate (melting point: 216 ° C) 1 part Carnauba wax 19 parts Evaflex 420 1 part (manufactured by Mitsui Polychemicals Co., Ltd.) Toluene 79 parts Then, a coating solution having the following composition was sufficiently dispersed at room temperature with an attritor, and The obtained ultraviolet absorbing ink was applied to a thickness of 1 μm on the cohesive failure layer by a gravure coating method.

エチレン−酢酸ビニル共重合体 1部 (三井ポリケミカル(株)製「エバフレックス577-
2」) カルナバワックス(野田ワックス(株)製「カルナバワ
ックスNo.1」) 19部 ベンゾトリアゾール(日本チバガイギー(株)製「TINU
VIN 900」) 0.5部 抗酸化剤(日本チバガイギー(株)製「IRGANOX 101
0」) 0.1部 トルエン 50部 メチルイソブチルケトン 29.4部 さらに、下記組成の塗液をアトライターにて常温で充
分に分散し、得られた近赤外線吸収インキを上記紫外線
吸収層の上にグラビアコート法にて塗布厚1.6μmに塗
布した。
Ethylene-vinyl acetate copolymer 1 part (Mitsui Polychemical Co., Ltd. "Evaflex 577-
2)) Carnauba wax ("Carnauba wax No.1" manufactured by Noda Wax Co., Ltd.) 19 parts Benzotriazole ("TINU" manufactured by Nippon Ciba Geigy Co., Ltd.)
VIN 900 ”) 0.5 parts Antioxidant (IRGANOX 101 manufactured by Ciba-Geigy Japan, Ltd.)
0 ”) 0.1 part Toluene 50 parts Methyl isobutyl ketone 29.4 parts Further, a coating liquid having the following composition was sufficiently dispersed at room temperature using an attritor, and the obtained near-infrared absorbing ink was coated on the ultraviolet absorbing layer by a gravure coating method. Was applied to a coating thickness of 1.6 μm.

エチレン−酢酸ビニル共重合体 1部 (三井ポリケミカル(株)製「エバフレックス577-
2」) カルナバワックス 19部 近赤外線吸収剤 0.2部 (ICIジャパン(株)製「PRO-JET IR SC101756」) トルエン 50部 メチルイソブチルケトン 29.8部 さらに、平均粒径0.5mmのガラスビーズが容積で60%
充填された5リットルのサンドミル中に予備混合した下
記組成物をギヤポンプによって2リットル/分の速度で
仕込み、サンドミルを10m/秒の速度で回転して混練を10
回繰り返し、得られた熱溶融性インキを上記近赤外線吸
収層の上にグラビアコート法にて塗布厚5μmに塗布
し、感熱転写材を得た。
Ethylene-vinyl acetate copolymer 1 part (Mitsui Polychemical Co., Ltd. "Evaflex 577-
2)) Carnauba wax 19 parts Near infrared absorber 0.2 parts (IC-Japan "PRO-JET IR SC101756") Toluene 50 parts Methyl isobutyl ketone 29.8 parts In addition, glass beads with an average particle diameter of 0.5 mm are 60 in volume. %
The following composition pre-mixed in a filled 5 liter sand mill was charged at a rate of 2 liters / minute by a gear pump, and the sand mill was rotated at a speed of 10 m / s to perform kneading.
This was repeated twice, and the resulting hot-melt ink was applied on the near-infrared absorbing layer to a coating thickness of 5 μm by a gravure coating method to obtain a thermal transfer material.

ライスワックス(野田ワックス(株)製「LP-200」)20
部 水性アクリル樹脂 8部 (東洋インキ製造(株)製「リオクリルAP-2」、固形分
27%) 水 40部 エタノール 29部 CIダイレクトレッド2 3部 (日本化薬(株)製「カヤラスベンゾパーブリン4B」) 得られた感熱転写材を用いて、バーコードラベルプリ
ンターでベック平滑度100秒の記録紙にバーコードを印
字したところ、耐光性に優れた艶消しのバーコード記録
物が得られ、読み取り波長780nmのバーコードリーダー
で読み取りが可能であった。また、記録物を晴天3日間
太陽光に曝したのち、分光光度計(島津製作所(株)
「UV-365」)にて780nmにおける反射率を測定したとこ
ろ、吸収率の低下は約8%であった。
Rice wax (“LP-200” manufactured by Noda Wax Co., Ltd.) 20
Part Water-based acrylic resin 8 parts (Toyo Ink Manufacturing Co., Ltd. “Riocryl AP-2”, solid content
27%) Water 40 parts Ethanol 29 parts CI Direct Red 2 3 parts (Nippon Kayaku Co., Ltd. "Kayaras benzoperbulin 4B") Using the obtained thermal transfer material, Beck smoothness with a bar code label printer When a barcode was printed on the recording paper for 100 seconds, a matte barcode record having excellent light resistance was obtained, and the barcode reader having a reading wavelength of 780 nm could read the barcode. After exposing the recorded matter to sunlight for three days in fine weather, a spectrophotometer (Shimadzu Corporation)
When the reflectance at 780 nm was measured using “UV-365”), the decrease in the absorptance was about 8%.

比較例1 実施例1の近赤外線吸収インキをグラビアコート法に
て6μmのポリエチレンテレフタレートフィルム上に塗
布厚5μmに塗布した。実施例1と同様の方法で評価し
たところ,読み取り波長780nmのバーコードリーダーで
読み取れたが,耐光性が悪く780nmにおける吸収率の低
下が約37%認められた。
Comparative Example 1 The near-infrared absorbing ink of Example 1 was applied to a 6 μm polyethylene terephthalate film by a gravure coating method to a coating thickness of 5 μm. When evaluated by the same method as in Example 1, the image was read with a bar code reader having a reading wavelength of 780 nm. However, the light resistance was poor and the absorption rate at 780 nm was reduced by about 37%.

比較例2 実施例1の近赤外線吸収層および熱溶融性インキ層を
グラビアコート法にて6μmのポリエチレンテレフタレ
ートフィルム上に塗布厚それぞれ1.6μmおよび5μm
に順次塗布した。実施例1と同様の方法で評価したとこ
ろ,読み取り波長780nmのバーコードリーダーで読み取
れたが,耐光性が悪く780nmにおける吸収率の低下が約3
0%認められた。
Comparative Example 2 The near-infrared absorbing layer and the hot-melt ink layer of Example 1 were coated on a 6 μm polyethylene terephthalate film by a gravure coating method to a thickness of 1.6 μm and 5 μm, respectively.
Was sequentially applied. When evaluated by the same method as in Example 1, the light was read by a bar code reader having a reading wavelength of 780 nm, but the light resistance was poor and the decrease in the absorptance at 780 nm was about 3%.
0% was observed.

(発明の作用および効果) 本発明の大きな特徴は、紫外線吸収剤を含む層を設け
て紫外線対策を施すことにより、太陽光に曝されても劣
化しない、耐光性に優れたバーコードが得られる点にあ
る。本発明の感熱転写材を用いれば、近赤外線を吸収検
出するバーコードリーダーにより読み取れる、耐光性に
優れたバーコード記録物を得ることができる。
(Functions and Effects of the Invention) A major feature of the present invention is that by providing a layer containing an ultraviolet absorbent and taking measures against ultraviolet rays, a bar code which does not deteriorate even when exposed to sunlight and has excellent light resistance can be obtained. On the point. By using the thermal transfer material of the present invention, it is possible to obtain a barcode record excellent in light resistance, which can be read by a barcode reader that absorbs and detects near infrared rays.

また、本発明の別の大きな特徴は、熱転写時に凝集破
壊を起こす層を有しているので、艶消し効果を有し、バ
ーコードリーダーによる読み取りが容易なバーコード記
録物が得られる点にある。
Another major feature of the present invention is that it has a layer that causes cohesive failure at the time of thermal transfer, has a matting effect, and is capable of obtaining a barcode record which is easy to read by a barcode reader. .

さらに、本発明の別の特徴は、近赤外線吸収剤を含む
層にカーボンブラック以外の着色剤を含有させることに
より、任意の色調の、製品のイメージに合う美しく高級
感のあるカラーのバーコード記録物が得られる点にあ
る。
Further, another feature of the present invention is that a layer containing a near-infrared absorbing agent contains a coloring agent other than carbon black, so that a bar code recording of a beautiful and high-grade color suitable for an image of a product in an arbitrary color tone. The point is that you can get things.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭63−159087(JP,A) 特開 昭64−30788(JP,A) 特開 昭61−57392(JP,A) 特開 昭60−85990(JP,A) 特開 昭64−1585(JP,A) 特開 昭63−60794(JP,A) 特開 昭59−224392(JP,A) ──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-63-159087 (JP, A) JP-A-64-30788 (JP, A) JP-A-61-57392 (JP, A) JP-A-60-1985 85990 (JP, A) JP-A-64-1585 (JP, A) JP-A-63-60794 (JP, A) JP-A-59-224392 (JP, A)

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】基材に、熱転写時に凝集破壊を起こす層、
紫外線吸収剤を含む熱溶融性インキ層および690〜1000n
mに吸収極大波長を有する、カーボンブラック以外の近
赤外線吸収剤を含む熱溶融性インキ層を順次設けてなる
ことを特徴とする黒以外のバーコード用感熱転写材。
A layer which causes cohesive failure during thermal transfer on a substrate;
Hot melt ink layer containing UV absorber and 690-1000n
A heat-sensitive transfer material for barcodes other than black, characterized in that a heat-meltable ink layer containing a near infrared absorbing agent other than carbon black having a maximum absorption wavelength at m is sequentially provided.
【請求項2】上記近赤外線吸収剤を含む層が、さらにカ
ーボンブラック以外の着色剤を含むことを特徴とする請
求項1記載の黒以外のバーコード用感熱転写材。
2. The heat-sensitive transfer material for barcodes other than black according to claim 1, wherein the layer containing the near-infrared absorbing agent further contains a coloring agent other than carbon black.
【請求項3】上記基材の熱溶融性インキ層と反対面に耐
熱保護層を形成してなる請求項1または2記載の黒以外
のバーコード用感熱転写材。
3. The heat-sensitive transfer material for barcodes other than black according to claim 1, wherein a heat-resistant protective layer is formed on the surface of the substrate opposite to the heat-meltable ink layer.
JP1168404A 1989-06-30 1989-06-30 Thermal transfer material Expired - Fee Related JP2579685B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1168404A JP2579685B2 (en) 1989-06-30 1989-06-30 Thermal transfer material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1168404A JP2579685B2 (en) 1989-06-30 1989-06-30 Thermal transfer material

Publications (2)

Publication Number Publication Date
JPH0334893A JPH0334893A (en) 1991-02-14
JP2579685B2 true JP2579685B2 (en) 1997-02-05

Family

ID=15867496

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1168404A Expired - Fee Related JP2579685B2 (en) 1989-06-30 1989-06-30 Thermal transfer material

Country Status (1)

Country Link
JP (1) JP2579685B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3019631B2 (en) * 1992-11-04 2000-03-13 松下電器産業株式会社 Document image printing device
US5576141A (en) * 1995-02-17 1996-11-19 Eastman Kodak Company Benzotriazole UV dyes for laser recording process
JP6425899B2 (en) * 2014-03-11 2018-11-21 デクセリアルズ株式会社 ANISOTROPIC CONDUCTIVE ADHESIVE, METHOD FOR MANUFACTURING CONNECTION AND METHOD FOR CONNECTING ELECTRONIC COMPONENTS

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59224392A (en) * 1983-06-04 1984-12-17 Canon Inc Thermal transfer material
JPS6085990A (en) * 1983-10-18 1985-05-15 Ricoh Co Ltd Enhancing fastness of image
JPS6157392A (en) * 1984-08-29 1986-03-24 Nec Corp Cover film for thermal transfer recording paper
JPS6360794A (en) * 1986-09-01 1988-03-16 Toppan Printing Co Ltd Thermal transfer recording medium
JP2634405B2 (en) * 1986-12-23 1997-07-23 ソニ−ケミカル株式会社 Thermal transfer recording medium
DE3808462C2 (en) * 1987-03-17 1996-04-25 Toyo Ink Mfg Co Heat-sensitive transfer material
JP2589701B2 (en) * 1987-07-27 1997-03-12 東洋インキ製造株式会社 Thermal transfer material

Also Published As

Publication number Publication date
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