JP2571851B2 - Thermal transfer material - Google Patents
Thermal transfer materialInfo
- Publication number
- JP2571851B2 JP2571851B2 JP1168405A JP16840589A JP2571851B2 JP 2571851 B2 JP2571851 B2 JP 2571851B2 JP 1168405 A JP1168405 A JP 1168405A JP 16840589 A JP16840589 A JP 16840589A JP 2571851 B2 JP2571851 B2 JP 2571851B2
- Authority
- JP
- Japan
- Prior art keywords
- heat
- layer
- transfer material
- thermal transfer
- ink layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000463 material Substances 0.000 title claims description 24
- 239000006096 absorbing agent Substances 0.000 claims description 14
- 239000006229 carbon black Substances 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims description 5
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 4
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 3
- 239000010410 layer Substances 0.000 claims 7
- 239000011241 protective layer Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- 239000012943 hotmelt Substances 0.000 description 12
- 239000001993 wax Substances 0.000 description 12
- -1 dithiol metal complex salts Chemical class 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 238000007756 gravure coating Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000004203 carnauba wax Substances 0.000 description 4
- 235000013869 carnauba wax Nutrition 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000012170 montan wax Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 239000011230 binding agent Substances 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
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- SUXCALIDMIIJCK-UHFFFAOYSA-L disodium;4-amino-3-[[4-[4-[(1-amino-4-sulfonatonaphthalen-2-yl)diazenyl]-3-methylphenyl]-2-methylphenyl]diazenyl]naphthalene-1-sulfonate Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(N=NC3=CC=C(C=C3C)C=3C=C(C(=CC=3)N=NC=3C(=C4C=CC=CC4=C(C=3)S([O-])(=O)=O)N)C)=CC(S([O-])(=O)=O)=C21 SUXCALIDMIIJCK-UHFFFAOYSA-L 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/385—Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; 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
- B41M5/46—Thermography ; 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; 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
- B41M5/46—Thermography ; 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
- B41M5/465—Infrared 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カラーの感熱転写材に関し,
目視識別が容易であると同時に見た目が美しく,高級感
のある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 relates to a color heat-sensitive transfer material having a layer containing a near-infrared absorber that selectively absorbs specific near-infrared rays.
The present invention relates to a heat-sensitive transfer material which is easy to visually recognize and has a beautiful appearance and gives a high-quality 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。また,人間が補助的に製品
の簡単な識別をすることですら非常に困難となる。(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 beauty of the product. Also, it is very difficult even for humans to easily identify products easily.
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,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。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。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, there is a disadvantage that the effect of the above is not sufficiently exhibited. 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,美観,耐光性に優れ,目視識
別を容易にしたカラーバーコード用感熱転写材を提供す
るものである。(Problems to be Solved by the Invention) The present inventors have conducted intensive studies on a method of producing a barcode other than black, and as a result, have found that the thermal transfer material for color barcodes has excellent aesthetics and light resistance and facilitates visual identification. Is provided.
(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、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およびカーボンブラック以外の着色
剤を含む熱溶融性着色インキ層を順次設けてなることを
特徴とするカラー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 provides a substrate comprising a layer which causes cohesive failure during thermal transfer, a heat-meltable ink layer containing a near infrared absorbing agent other than carbon black, and a coloring agent other than carbon black. The present invention relates to a heat-sensitive transfer material for color barcodes, which is provided with a heat-meltable colored ink layer in order.
本発明の感熱転写材は、熱溶融性着色インキ層に任意
の色材を使うことができるので、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、目視識
別を容易にすると共に、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、各種製品に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 can use any color material for the heat-meltable colored ink layer, it is easy to visually identify when recording with a thermal head using the heat-sensitive transfer material of the present invention. At the same time, it is possible to obtain a beautiful and high-quality color barcode recorded matter that matches the image of the product. The barcode recorded material can be read by a normal barcode reader that absorbs and detects near-infrared rays, and is effective for collation of manufacturing lot numbers and product numbers assigned to various products for product management.
上記熱溶融性着色インキ層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。The coloring materials that can be used for the hot-melt colored ink layer are red,
Green, blue, yellow, red, indigo dyes / pigments, pastel / white / pearl pigments, fluorescent dyes, gold / silver metal powders, etc., are not particularly limited.
本発明の近赤外線とは通常690〜2500nm範囲の電磁波
を指すが,本発明では波長690〜1000nmに主波長を有す
る近赤外線を利用することが好ましい。The near-infrared ray of the present invention generally refers to an electromagnetic wave in the range of 690 to 2500 nm, but in the present invention, it is preferable to use near-infrared rays having a main wavelength of 690 to 1000 nm.
本発明による近赤外線吸収剤としては従来公知の波長
690〜1000nm範囲の電磁波を吸収するもので,たとえば
表1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。Known near-infrared absorbers according to the present invention
It absorbs electromagnetic waves in the range of 690 to 1000 nm, and includes, for example, compounds of the chemical structural formulas shown in Table 1, dithiol metal complex salts, anthraquinones, mercaptonnaphthol metal complex salts, naphthoquinones, cyanine dyes, and the like.
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.
近赤外線吸収剤を含む感熱転写材による記録物を太陽
光線にさらすと,紫外線の効果によって劣化し充分な効
果が得られなくなる。これらのことを防止する為,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の
間に紫外線吸収剤を含む層を設けることができる。本発
明の紫外線吸収剤は,290〜400nmの有害な紫外線を吸収
する作用をもつもので,たとえば表2の化合物をあげる
ことができる。 When a recording material made of a thermal transfer material containing a near-infrared absorbing agent is exposed to sunlight, it deteriorates due to the effect of ultraviolet rays, and a sufficient effect cannot be obtained. In order to prevent these, a layer containing an ultraviolet absorber can be provided between a layer causing cohesive failure during thermal transfer and a layer containing a near-infrared absorber. The ultraviolet absorber of the present invention has a function of absorbing harmful ultraviolet light of 290 to 400 nm, and examples thereof include the compounds shown in Table 2.
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、その破壊表面の凹
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号の明細書に開示してい
る。 The layer that causes cohesive failure during thermal transfer causes cohesive failure when transferring and peeling the hot-melt ink layer, and the unevenness of the destruction surface gives a matte effect to the barcode recorded material, 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 the specification of Japanese Patent Application No. 62-60215.
本発明の近赤外線吸収層,熱溶融性着色インキ層,紫
外線吸収層,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。塗布量は,0.1μm及至3μm
が適当である。0.1μm以下だと各層の効果が少なくな
り,3μm以上では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 near-infrared absorbing layer, hot-melt colored ink layer, ultraviolet absorbing layer and cohesive failure layer of the present invention on a substrate, a hot melt coating method or more preferably a coating method in which the above compound is dispersed in a medium is used. There is a method of solvent-coating the liquid. Coating amount: 0.1μm to 3μm
Is appropriate. If it is less than 0.1 μm, the effect of each layer is reduced, and if it is more than 3 μm, the total coating thickness becomes large, and when the transfer material is wound into a roll, the winding becomes thick and the energy sensitivity decreases.
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は,従来公知の組成成分を
そのまま用いることができる。ワックスおよび熱可塑性
樹脂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, a conventionally known composition component can be used as it is. Examples thereof include those colored with the above-mentioned dyes and pigments using wax and thermoplastic resin 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-hydroxystearin Examples of fatty acids such as acids, waxes such as fatty acid amides, fatty acid anilides and imido wax, and resins include:
Acrylic, styrene, rosin, vinyl, acetal, and rubber are preferred.
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 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、紫外線吸収インキを得て、得られたインキ
を凝集破壊層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 Toluene 79 parts Then, a coating liquid having the following composition is sufficiently dispersed at room temperature with an attritor to obtain an ultraviolet absorbing ink. The resulting ink was applied on the cohesive failure layer to a coating thickness of 1 μm by a gravure coating method.
エチレン−酢酸ビニル共重合体 1部 カルナバワックス 19部 紫外線吸収剤(日本チバガイギー(株)製「TINUVIN 90
0」) 0.5部 トルエン 50部 メチルイソブチルケトン 29.5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、近赤外線吸収インキを得て、得られたイン
キを紫外線吸収層上にグラビアコート法にて塗布厚1.6
μmに塗布した。Ethylene-vinyl acetate copolymer 1 part Carnauba wax 19 parts UV absorber ("TINUVIN 90" manufactured by Nippon Ciba Geigy Co., Ltd.)
0 ") 0.5 parts Toluene 50 parts Methyl isobutyl ketone 29.5 parts Further, a coating liquid having the following composition was sufficiently dispersed at room temperature with an attritor to obtain a near-infrared absorbing ink, and the obtained ink was placed on the ultraviolet absorbing layer. Coating thickness 1.6 by gravure coating method
μm.
エチレン−酢酸ビニル共重合体 (三井ポリケミカル(株)製「エバフレックス」)1部 カルナバワックス(野田ワックス(株)製) 19部 近赤外線吸収剤(ICI製「SC101756」) 0.2部 トルエン 50部 メチルイソブチルケトン 29.5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
回繰り返して熱溶融性インキを得て、得られたインキを
近赤外線吸収層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 (Evaflex manufactured by Mitsui Polychemicals Co., Ltd.) 1 part Carnauba wax (Noda Wax Co., Ltd.) 19 parts Near infrared absorber (ICI "SC101756") 0.2 parts Toluene 50 parts 29.5 parts of methyl isobutyl ketone 60% glass beads with an average particle size of 0.5 mm
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.
Repeat the process to obtain a hot-melt ink, and apply the obtained ink on the near-infrared absorbing layer by a gravure coating method to a thickness of 5 μm.
To obtain a heat-sensitive 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 (東洋インキ製造(株)製「リオクリルAP−2」、固形
分27%) 8部 水 40部 エタノール 29部 CIダイレクトレッド2(日本化薬(株)製「パーブリン
4B」) 3部 得られた感熱転写材を用いてバーコードラベルプリン
ターでバーコードを印字したところ,艶消しのバーコー
ド印字物が得られ,読取り波長780nmのバーコードリー
ダーにて読取りが可能であった。Rice wax (“LP-200” manufactured by Noda Wax Co., Ltd.) 20 parts Aqueous acrylic resin (“Riocryl AP-2” manufactured by Toyo Ink Mfg. Co., Ltd., solid content 27%) 8 parts Water 40 parts Ethanol 29 parts CI Direct Red 2 ("Nippon Kayaku Co., Ltd."
4B ”) 3 copies When the barcode was printed with a barcode label printer using the obtained thermal transfer material, a matte barcode print was obtained, which could be read by a barcode reader with a reading wavelength of 780 nm. there were.
比較例1 実施例1の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,読み取れず780nmにおける反射率は97%であっ
た。Comparative Example 1 The hot-melt ink layer of Example 1 was applied to a 6 μm polyethylene terephthalate film with a coating thickness of 5 μm by a gravure coating method. When evaluated in the same manner as in Example 1, no reading was performed, and the reflectance at 780 nm was 97%.
比較例2 実施例3の熱溶融性インキ層をロールコート法にて6
μm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,読取り波長780nmのバーコードリーダーで読み取
れず780nmにおける反射率は98%であった。Comparative Example 2 The hot-melt ink layer of Example 3 was coated with
It was applied to a coating thickness of 5 μm on a polyethylene terephthalate film of μm. When evaluated by the same method as in Example 1, it could not be read by a barcode reader having a reading wavelength of 780 nm, and the reflectance at 780 nm was 98%.
(発明の作用および効果) 本発明の大きな特徴は、熱溶融性着色インキ層に任意
の色材を使うことができるので、黒以外の任意の色のカ
ラー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、目視識別を容易にすると共に、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
録物を得ることができる。(Function and Effect of the Invention) A major feature of the present invention is that any color material can be used for the hot-melt colored ink layer, and thus a color barcode of any color other than black can be obtained. When the thermal transfer material of the present invention is used, it is possible to facilitate visual identification and obtain a beautiful and high-quality color barcode recorded matter that matches the image of the product.
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、熱転写時に凝集破壊を
起こす層と近赤外線吸収層との間に紫外線吸収剤を含む
層を設けることにより、近赤外線吸収剤の紫外線による
劣化を抑えることができる点にある。Further, another feature of the present invention is that by providing a layer containing an ultraviolet absorber between the layer that causes cohesive failure at the time of thermal transfer and the near infrared absorption layer, deterioration of the near infrared absorber by ultraviolet light can be suppressed. On the point.
Claims (4)
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
インキ層およびカーボンブラック以外の着色剤を含む熱
溶融性着色インキ層を順次設けてなることを特徴とする
カラーバーコード用感熱転写材。A layer which causes cohesive failure during thermal transfer on a substrate;
A heat-sensitive transfer material for color barcodes, comprising a heat-meltable ink layer containing a near-infrared absorbing agent other than carbon black and a heat-meltable colored ink layer containing a colorant other than carbon black.
極大波長を有することを特徴とする請求項1記載のカラ
ーバーコード用感熱転写材。2. The heat-sensitive transfer material for color barcodes according to claim 1, wherein said near-infrared absorbing agent has an absorption maximum wavelength at 690 to 1000 nm.
吸収剤を含む熱溶融性インキ層との間に、紫外線吸収剤
を含む層を設けてなることを特徴とする請求項1または
2記載のカラーバーコード用感熱転写材。3. A layer containing an ultraviolet absorber is provided between a layer which causes cohesive failure during thermal transfer and a heat-meltable ink layer containing a near infrared absorber. Thermal transfer material for color barcodes.
熱保護層を形成してなる請求項1ないし3記載のカラー
バーコード用感熱転写材。4. The heat-sensitive transfer material for color barcodes according to claim 1, wherein a heat-resistant protective layer is formed on the surface of the base material opposite to the heat-meltable ink layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1168405A JP2571851B2 (en) | 1989-06-30 | 1989-06-30 | Thermal transfer material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1168405A JP2571851B2 (en) | 1989-06-30 | 1989-06-30 | Thermal transfer material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0334894A JPH0334894A (en) | 1991-02-14 |
JP2571851B2 true JP2571851B2 (en) | 1997-01-16 |
Family
ID=15867516
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1168405A Expired - Fee Related JP2571851B2 (en) | 1989-06-30 | 1989-06-30 | Thermal transfer material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2571851B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03173691A (en) * | 1989-12-01 | 1991-07-26 | Toyo Ink Mfg Co Ltd | Thermosensitive transfer material |
US5576141A (en) * | 1995-02-17 | 1996-11-19 | Eastman Kodak Company | Benzotriazole UV dyes for laser recording process |
JP6443786B1 (en) * | 2017-08-24 | 2018-12-26 | 大日本印刷株式会社 | Thermal transfer sheet |
WO2019038960A1 (en) * | 2017-08-24 | 2019-02-28 | 大日本印刷株式会社 | Thermal transfer sheet |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
-
1989
- 1989-06-30 JP JP1168405A patent/JP2571851B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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JPH0334894A (en) | 1991-02-14 |
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