JPH03218892A - Thermal transfer recording material - Google Patents
Thermal transfer recording materialInfo
- Publication number
- JPH03218892A JPH03218892A JP2013961A JP1396190A JPH03218892A JP H03218892 A JPH03218892 A JP H03218892A JP 2013961 A JP2013961 A JP 2013961A JP 1396190 A JP1396190 A JP 1396190A JP H03218892 A JPH03218892 A JP H03218892A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- vinyl acetate
- ethylene
- acetate copolymer
- paper
- 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
- 239000000463 material Substances 0.000 title claims abstract description 29
- 238000012546 transfer Methods 0.000 title claims description 20
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 26
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 25
- 239000000123 paper Substances 0.000 abstract description 30
- 239000011230 binding agent Substances 0.000 abstract description 14
- 239000006185 dispersion Substances 0.000 abstract description 10
- 229920001577 copolymer Polymers 0.000 abstract description 5
- 239000003086 colorant Substances 0.000 abstract description 3
- 239000004952 Polyamide Substances 0.000 abstract description 2
- 239000004642 Polyimide Substances 0.000 abstract description 2
- 239000011086 glassine Substances 0.000 abstract description 2
- 229920003023 plastic Polymers 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 abstract description 2
- 229920002647 polyamide Polymers 0.000 abstract description 2
- 239000004417 polycarbonate Substances 0.000 abstract description 2
- 229920000515 polycarbonate Polymers 0.000 abstract description 2
- 229920000728 polyester Polymers 0.000 abstract description 2
- 229920001721 polyimide Polymers 0.000 abstract description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 4
- 239000005977 Ethylene Substances 0.000 abstract 4
- 238000002844 melting Methods 0.000 description 14
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 12
- 239000001993 wax Substances 0.000 description 10
- 239000012943 hotmelt Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 7
- 239000006229 carbon black Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000012188 paraffin wax Substances 0.000 description 5
- CJYDNDLQIIGSTH-UHFFFAOYSA-N 1-(3,5,7-trinitro-1,3,5,7-tetrazocan-1-yl)ethanone Chemical compound CC(=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 CJYDNDLQIIGSTH-UHFFFAOYSA-N 0.000 description 4
- 239000004204 candelilla wax Substances 0.000 description 4
- 235000013868 candelilla wax Nutrition 0.000 description 4
- 229940073532 candelilla wax Drugs 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
- 150000004665 fatty acids Chemical class 0.000 description 4
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000004203 carnauba wax Substances 0.000 description 3
- 235000013869 carnauba wax Nutrition 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 238000007756 gravure coating Methods 0.000 description 3
- 239000004200 microcrystalline wax Substances 0.000 description 3
- 235000019808 microcrystalline wax Nutrition 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004166 Lanolin Substances 0.000 description 2
- 241001147388 Uncia Species 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000010365 information processing Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- 229940039717 lanolin Drugs 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012169 petroleum derived wax Substances 0.000 description 2
- 235000019381 petroleum wax Nutrition 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- OSNILPMOSNGHLC-UHFFFAOYSA-N 1-[4-methoxy-3-(piperidin-1-ylmethyl)phenyl]ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1CN1CCCCC1 OSNILPMOSNGHLC-UHFFFAOYSA-N 0.000 description 1
- RVNAQNUKCZKJCP-UHFFFAOYSA-N 2,3-dihydroxypropyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(O)CO RVNAQNUKCZKJCP-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- PZTQVMXMKVTIRC-UHFFFAOYSA-L chembl2028348 Chemical compound [Ca+2].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 PZTQVMXMKVTIRC-UHFFFAOYSA-L 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000010187 litholrubine BK Nutrition 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 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
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 229940012185 zinc palmitate Drugs 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- GJAPSKMAVXDBIU-UHFFFAOYSA-L zinc;hexadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O GJAPSKMAVXDBIU-UHFFFAOYSA-L 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)
本発明はサーマルプリンターなどの感熱転写型記録装置
に用いられる感熱転写型記録材に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a thermal transfer recording material used in a thermal transfer recording device such as a thermal printer.
(従来の技術)
近年、情報産業の急速な発展にともない種々の情報処理
システムが出現し、又、それぞれの情報処理システムに
適した記録方法およびその装置が開発されている。(Prior Art) In recent years, with the rapid development of the information industry, various information processing systems have appeared, and recording methods and devices suitable for each information processing system have been developed.
このような記録方法の一つとして、記録紙と感熱転写型
記録材の熱溶融性インキ層とを接触させ、加圧し、基材
の裏面にサーマルヘッドを接触させて該ヘッドにパルス
状に電気信号を送り、ヘッドを加熱することによって加
熱された箇所の熱転写層における熱溶融性インキを転写
させて印字する感熱転写記録方法があり、この方法は、
使用する装置が軽量かつコンパクトで騒音がなく操作性
、保守性にも優れていることから最近益々汎用されてい
る。One such recording method involves bringing the recording paper into contact with the heat-melting ink layer of the thermal transfer type recording material, applying pressure, and then bringing a thermal head into contact with the back side of the base material to apply pulsed electricity to the head. There is a thermal transfer recording method that prints by sending a signal and heating the head to transfer the heat-melting ink on the heated area of the thermal transfer layer.
Recently, it has become increasingly popular because the equipment used is lightweight, compact, noiseless, and has excellent operability and maintainability.
(発明が解決しようとする課題)
しかしながら、本方式は基本的に記録紙と感熱転写型記
録材との接触による印字方式を採用しているため、記録
紙として高平滑紙を使用した場合には問題ないが、表面
の凹凸が激しい一般紙(例えば、上質紙、乾式複写機用
用紙など)を使用した場合、その印字が不鮮明(例えば
、文字の一部が欠損してしまう等)となり、従って、専
用の高平滑紙を使用しなければならないという不利益を
有していた。(Problem to be Solved by the Invention) However, since this method basically uses a printing method that involves contact between recording paper and thermal transfer type recording material, when highly smooth paper is used as the recording paper, This is not a problem, but if you use general paper with a highly uneven surface (e.g., high-quality paper, dry copying machine paper, etc.), the print will be unclear (e.g., some of the characters will be missing), and the However, this method had the disadvantage of requiring the use of specialized highly smooth paper.
(課題を解決するための手段)
本発明は、上記した事情に鑑みなされたもので,専用の
高平滑紙を用いることなく一般紙においても良好な印字
性能を得るべく鋭意研究を重ねた結果、凹凸の激しい一
般紙の凸部間に架橋構造を形成させ得るよう熱溶融性イ
ンキを設計することにより、一般紙への印字が可能とな
る知見を得、前記架橋構造を形成させる手段として、前
記熱溶融性インキ層にエチレン−酢酸ビニル共重合体の
均一分散状態を形成せしめたものが最適であることを見
いだし、遂に本発明を完成したもので、基材と該基材上
に設けられた熱溶融性インキ層から少なくともなる感熱
転写型記録材において、前記熱溶融性インキ層に、エチ
レン−酢酸ビニル共重合体の均一分散状態を形成せしめ
ることを特徴とする感熱転写型記録材を要旨とするもの
である。(Means for Solving the Problems) The present invention was made in view of the above-mentioned circumstances, and as a result of intensive research to obtain good printing performance even on general paper without using special highly smooth paper. By designing a heat-melting ink to form a crosslinked structure between the convex portions of highly uneven general paper, we have discovered that it is possible to print on general paper, and as a means for forming the crosslinked structure, we have developed the It was discovered that the most suitable one was one in which a hot-melt ink layer was formed in a uniformly dispersed state of ethylene-vinyl acetate copolymer, and the present invention was finally completed. The present invention provides a heat-sensitive transfer recording material comprising at least a heat-melt ink layer, characterized in that an ethylene-vinyl acetate copolymer is uniformly dispersed in the heat-melt ink layer. It is something to do.
以下、本発明を詳述する。The present invention will be explained in detail below.
本発明における基材は、グラシン紙、コンデンサ紙等の
紙類、あるいはポリエステル、ボリカーボーネイト、ポ
リイミド、ポリアミド等のプラスチック類が使用できる
。As the base material in the present invention, papers such as glassine paper and capacitor paper, or plastics such as polyester, polycarbonate, polyimide, and polyamide can be used.
基材上に設けられる熱溶融性インキ層は、熱溶融性バイ
ンダー,均一分散状態を形成しているエチレン−酢酸ビ
ニル共重合体、柔軟材、着色材がその主成分となるもの
である。The heat-melt ink layer provided on the base material is mainly composed of a heat-melt binder, a uniformly dispersed ethylene-vinyl acetate copolymer, a softener, and a coloring material.
熱溶融性バインダーは、パラフィンワックス、マイクロ
クリスタリンワックス等の石油ワックスやポリエチレン
ワックス等の極性を持たないワックス類,キャンデリラ
ワックス等の中程度の極性を持つワックス類、カルナウ
バワックス、木蝋、蜜蝋、エステルワックス等の大きな
極性を持つワックス類及びステアリン酸、パルミチン酸
、ラウリン酸、ステアリン酸アルミニウム、パルミチン
酸亜鉛、グリセロールモノヒドロキシステアレート、オ
レイン酸アミド,ステアリン酸アミド、ラノリン脂肪酸
などの高級脂肪酸、或いはその金属塩、エステル、アミ
ドなどの誘導体などといった大きな極性を持つものが1
種類若しくは2種類以上混合して使用される。Heat-melting binders include petroleum waxes such as paraffin wax and microcrystalline wax, non-polar waxes such as polyethylene wax, moderately polar waxes such as candelilla wax, carnauba wax, wood wax, beeswax, Highly polar waxes such as ester waxes and higher fatty acids such as stearic acid, palmitic acid, lauric acid, aluminum stearate, zinc palmitate, glycerol monohydroxystearate, oleic acid amide, stearic acid amide, and lanolin fatty acids; Those with large polarity such as metal salts, esters, amides, and other derivatives are 1
It can be used in different types or in a mixture of two or more types.
本発明の特徴点は、エチレン−酢酸ビニル共重合体を熱
溶融性インキ層中に均一分散することにあり、均一分散
状態とは,熱溶融性インキ層中にエチレン−酢酸ビニル
共重合体の微粒子が均一に散在している状態をいう。従
って、エチレン−酢酸ビニル共重合体を熱溶融性インキ
層中に均一分散するためにはエチレン−酢酸ビニル共重
合体と熱溶融性バインダーとが相溶も分離もしないよう
各々の極性を調整する必要がある。The feature of the present invention is that the ethylene-vinyl acetate copolymer is uniformly dispersed in the hot-melt ink layer. A state in which fine particles are uniformly scattered. Therefore, in order to uniformly disperse the ethylene-vinyl acetate copolymer in the heat-fusible ink layer, the polarity of each must be adjusted so that the ethylene-vinyl acetate copolymer and the heat-fusible binder do not dissolve or separate. There is a need.
例えば、熱溶融性バインダーとして極性を持たないワッ
クスを用いた場合、酢酸ビニル含有量が30%以下(低
〜中程度の極性)のエチレン−酢酸ビニル共重合体は相
溶してしまい、均一な分散状態は得られず、酢酸ビニル
含有量が30%を越える極性の大きいエチレン−酢酸ビ
ニル共重合体は相溶せず、エチレン−酢酸ビニル共重合
体の分離が発生してしまい、所望の均一な分散状態は得
られない。即ち、一般に、極性が近いもの同志は相溶性
が良好であり、極性が遠いもの同志は相溶が良くないと
いえる。For example, when a non-polar wax is used as a hot-melt binder, an ethylene-vinyl acetate copolymer with a vinyl acetate content of 30% or less (low to medium polarity) will be miscible, resulting in a uniform A highly polar ethylene-vinyl acetate copolymer with a vinyl acetate content exceeding 30% is not compatible with the ethylene-vinyl acetate copolymer, and separation of the ethylene-vinyl acetate copolymer occurs, resulting in the desired uniformity. A well-distributed state cannot be obtained. That is, in general, substances with close polarities have good compatibility, and substances with far polarities have poor compatibility.
一方、熱溶融性バインダーの極性は、石油ワックスのよ
うな極性を持たないワックスと、分子中にエステル結合
やOH基あるいは遊離脂肪酸を有することにより極性を
持つワックス、あるいは高級脂肪酸及びその金属塩,界
面活性剤などを混合することにより任意に調整すること
が可能であり、エチレン−酢酸ビニル共重合体の極性は
、その酢酸ビニルの含有量により変化し,酢酸ビニル含
有量が増加すると共に極性は増加し,酢酸ビニルの含有
量が減少すると共に極性は低下する。従って、エチレン
−酢酸ビニル共重合体を熱溶融性バインダーに相溶又は
分離させることなく、その中間的な状態である均一な分
散状態となすには、エチレン−酢酸ビニル共重合体の極
性と熱溶融性バインダーの極性とを調整することにより
、所望する均一な分散状態を得ることが出来る。On the other hand, the polarity of heat-melting binders is determined by waxes that have no polarity such as petroleum wax, waxes that have polarity due to having ester bonds, OH groups, or free fatty acids in their molecules, or higher fatty acids and their metal salts. It can be adjusted arbitrarily by mixing surfactants, etc. The polarity of the ethylene-vinyl acetate copolymer changes depending on the vinyl acetate content, and as the vinyl acetate content increases, the polarity decreases. The polarity decreases as the vinyl acetate content decreases. Therefore, in order to make the ethylene-vinyl acetate copolymer compatible with the heat-melting binder or to achieve a uniform dispersion state that is an intermediate state between the two, the polarity of the ethylene-vinyl acetate copolymer and the thermal By adjusting the polarity of the meltable binder, a desired uniform dispersion state can be obtained.
本発明において使用されるエチレン−酢酸ビニル共重合
体としては、EVAFLEX150 (酢酸ビニル含有
量:33wt%、以下同じ)、同40Y (41wt%
)、同45X (46wt%)、同220 (28wt
%)、同260 (28wt%)、同360 (25w
t%)、同420 (19wt%)、同460 (19
wt%)(以上、三井デュポンボリケミカル■製)、ソ
アレックスBH (55wt%)、同CH (60wt
%),同DI (67wt%)、同DH(67wt%)
、同FH (87wt%)、同BI (55wt%)、
同CI(60wt%)(以上、日本合成化学工業■製)
、NUCコポリマーMB 080(19wt%)、同
MB−850 (22wt%)、同MB−010(2
5 w t%)、同MB−030 (27wt%)(以
上、日本ユニカ一一製)などの商品名で市販されている
ものであるが、本発明では特にこれらに限定されること
なく使用でき、極性の大きなエチレン−酢酸ビニル共重
合体、具体的には酢酸ビニル含有量が30wt%を越え
るものを使用した場合,熱溶融性バインダーは極性を持
たないワックスを主成分とし、30wt%以下のものの
場合、極性の大きなものを主成分とする。Ethylene-vinyl acetate copolymers used in the present invention include EVAFLEX 150 (vinyl acetate content: 33 wt%, the same applies hereinafter), EVAFLEX 40Y (41 wt%)
), 45X (46wt%), 220 (28wt%)
%), 260 (28wt%), 360 (25w
t%), 420 (19wt%), 460 (19wt%)
wt%) (manufactured by Mitsui DuPont Bolichemical ■), Solex BH (55wt%), Solex CH (60wt%)
%), DI (67wt%), DH (67wt%)
, FH (87wt%), BI (55wt%),
The same CI (60wt%) (manufactured by Nippon Gosei Kagaku Kogyo ■)
, NUC copolymer MB 080 (19 wt%), MB-850 (22 wt%), MB-010 (2
5 wt%) and MB-030 (27 wt%) (manufactured by Nippon Unica Ichiichi), but the present invention is not limited to these and can be used. When a highly polar ethylene-vinyl acetate copolymer, specifically one with a vinyl acetate content of more than 30 wt%, is used, the heat-melting binder is mainly composed of non-polar wax and contains less than 30 wt% of vinyl acetate. In the case of substances, the main component is one with high polarity.
エチレン−酢酸ビニル共重合体の使用量は、熱溶融性イ
ンキ100重量部に対して5〜15重量部とすることが
好ましく、これらは2種以上混合して使用することも可
能である。The amount of the ethylene-vinyl acetate copolymer used is preferably 5 to 15 parts by weight per 100 parts by weight of the hot-melt ink, and two or more of these can also be used in combination.
柔軟材としては、石油樹脂、ポリ酢酸ビニル、ボリスチ
レン、スチレンブタジエン共重合体、アクリル系樹脂な
どの樹脂類があげられる。Examples of the flexible material include resins such as petroleum resin, polyvinyl acetate, polystyrene, styrene-butadiene copolymer, and acrylic resin.
着色材としては、各種グレードのカーボンブラック等の
黒色顔料、ベンジジンイエロー、ハンザイエロー、ジン
クイエロー等の黄色顔料、パーマネントラット4R、ロ
ーダミンレーキP、ブリリアントカーミン6B等の赤色
顔料、ビクトリアブルーレーキ、フタロシアニンブルー
、ファーストスカイブルー等の青色顔料が用いられる。Colorants include black pigments such as various grades of carbon black, yellow pigments such as Benzidine Yellow, Hansa Yellow, and Zinc Yellow, red pigments such as Permanent Rat 4R, Rhodamine Lake P, and Brilliant Carmine 6B, Victoria Blue Lake, and Phthalocyanine Blue. , Fast Sky Blue, and other blue pigments are used.
熱溶融性インキ層における各成分の使用量は、総重量1
00部に対して熱溶融性バインダー30〜80部、エチ
レン−酢酸ビニル共重合体5〜15重量部、柔軟剤3〜
20部、着色材5〜20部とすることが好ましく、他に
少量の酸化防止剤、分散剤、滑剤等を添加しても良い。The amount of each component used in the hot-melt ink layer is based on the total weight of 1
00 parts, 30 to 80 parts of heat-melting binder, 5 to 15 parts by weight of ethylene-vinyl acetate copolymer, 3 to 10 parts of softener
It is preferable to use 20 parts and 5 to 20 parts of colorant, and small amounts of antioxidants, dispersants, lubricants, etc. may also be added.
本発明の感熱転写型記録材は,上記各成分を加温された
三本ロール、アトライター等の周知の混合分散機を用い
て熱溶融性インキを調製し、これをそのまま、又は、適
当な濃度に分散させたものを,基材に、例えば、ロール
コーティング法,ファウンテンコーティング法、グラビ
アコーティング法、スクリーンコーティング法など種々
の塗布方法によって、その塗布厚が2〜15μmとなる
よう塗布することにより得ることができる。The heat-sensitive transfer type recording material of the present invention is prepared by preparing a heat-melting ink using a well-known mixing and dispersing machine such as a heated triple roll or an attriter using each of the above-mentioned components, and then using the heat-melting ink as it is or in a suitable form. By applying the dispersed product to a base material at a coating thickness of 2 to 15 μm using various coating methods such as roll coating, fountain coating, gravure coating, and screen coating. Obtainable.
尚、本発明においては基材と熱溶融性インキ層との間に
、更に離型層を設けたり、また、基材真面に耐熱層を設
けること勿論である。In the present invention, it goes without saying that a release layer may be further provided between the base material and the heat-fusible ink layer, and a heat-resistant layer may be provided directly in front of the base material.
(作用)
本発明では特に、熱溶融性インキ層にエチレン−酢酸ビ
ニル共重合体の微粒子が均一に分散しているため、表面
の凹凸が激しい一般紙に印字する際において、この微粒
子が凸部間に架橋するように働くため、熱溶融性インキ
層が凹部をも被覆することとなり、よって専用の高平滑
紙を用いることなくとも良好な印字特性が得られるもの
である。(Function) In particular, in the present invention, since fine particles of ethylene-vinyl acetate copolymer are uniformly dispersed in the heat-melting ink layer, when printing on general paper with a highly uneven surface, these fine particles can Since the heat-melting ink layer acts as a bridge between the two, the heat-melting ink layer also covers the concave portions, and good printing characteristics can therefore be obtained without using special highly smooth paper.
(実施例)
以下、本発明を実施例に基き更に詳細に説明するが、実
施例中「部」とあるのは「重量部を」示す。(Example) Hereinafter, the present invention will be explained in more detail based on Examples, where "parts" in the examples indicate "parts by weight."
実施例1
カーボンブラック 120部(Ra
ven#1035、
コロンビアン・カーボンジャパン■製)マイクロクリス
タリンワックス 400部(極性:無し、H i
M i c 2 0 6 5、日本精蝋■製)
キャンデリラワックス 360部(極性:
中、野田ワックス■製)
分散剤 20部(ソルス
パース 17000、
ICIジャパン■製)
EVAFLEX45X 100部(エチレ
ン−酢酸ビニル共重合体、酢酸ビニル含有量:46wt
%、三井デュポンボリケミカル■製)
上記各成分を三本ロールにより加温分散させ熱溶融性イ
ンキを!l!ljlIIシ,これを厚さ4.5μmのポ
リエステルフィルム上にグラビアコーティング法によっ
て塗布厚さが5μmとなるよう塗布し感熱転写型記録材
を得た。Example 1 Carbon black 120 parts (Ra
ven#1035, manufactured by Columbian Carbon Japan ■) Microcrystalline wax 400 parts (Polarity: None, Hi
Mic2065, made by Nippon Seiro ■) Candelilla wax 360 parts (Polarity:
Medium, manufactured by Noda Wax ■) Dispersant 20 parts (Solsperse 17000, manufactured by ICI Japan ■) EVAFLEX45X 100 parts (ethylene-vinyl acetate copolymer, vinyl acetate content: 46 wt
%, manufactured by DuPont Mitsui Polychemical ■) Each of the above ingredients is heated and dispersed using three rolls to create a heat-melting ink! l! This was coated onto a 4.5 μm thick polyester film by gravure coating to a coating thickness of 5 μm to obtain a heat-sensitive transfer type recording material.
実施例2
カーボンブラック 120部パラフ
ィンワックス 510部(極性:無し
、155゜F、日本精蝋■製)カルナバワックス
150部(極性二大、野田ワックス■製
)
EVAFLEX150 150部(エチ
レン−酢酸ビニル共重合体、酢酸ビニル含有量: 33
wt%、三井デュポンボリケミカル■製)
石油樹脂 50部(エス
コレッツ 5380、米国、エクソン化学社製)
分散剤 (ソルスパース17000) 20部上記
各成分を実施例1と同様になして感熱転写型記録材を得
た。Example 2 Carbon black 120 parts Paraffin wax 510 parts (Polarity: None, 155°F, manufactured by Nippon Seiro ■) Carnauba wax
150 parts (Polar Two, manufactured by Noda Wax ■) EVAFLEX150 150 parts (ethylene-vinyl acetate copolymer, vinyl acetate content: 33
wt%, manufactured by DuPont Mitsui Polychemical Co., Ltd.) Petroleum resin 50 parts (Escolettes 5380, manufactured by Exxon Chemical Co., USA) Dispersant (Solsperse 17000) 20 parts The above components were prepared in the same manner as in Example 1 to prepare a thermal transfer recording material. I got it.
実施例3
カーボンブラック 120部パラフ
ィンワックス 450部(極性:無し
、155゜F、日本精蝋■製)キャンデリラワックス
250部(極性二大、野田ワックス■製
)
ラノリン脂肪酸 50部(SK
LIRO、クローダジャパン■製)ソアレックスCH
110部(エチレン−酢酸ビニル
共重合体、酢酸ビニル含有量: 60wt%、日本合成
化学工業■製)分散剤 (ソルスパース17000)
20部上記各成分を実施例1と同様になして感熱転
写型記録材を得た。Example 3 Carbon black 120 parts Paraffin wax 450 parts (Polarity: None, 155°F, manufactured by Nippon Seiro) Candelilla wax
250 parts (Polar Two, manufactured by Noda Wax ■) Lanolin fatty acid 50 parts (SK
LIRO, made by Croda Japan ■) Solex CH
110 parts (ethylene-vinyl acetate copolymer, vinyl acetate content: 60 wt%, manufactured by Nippon Gosei Kagaku Kogyo ■) Dispersant (Solsperse 17000)
20 parts A heat-sensitive transfer type recording material was obtained using the above components in the same manner as in Example 1.
実施例4
実施例1で調製した熱溶融性インキを100℃に加温し
、これに芳香族系混合溶剤(ペガソールR−100,モ
ービル石油■製)を3000重量部加え撹拌した後、放
冷し、このインキの微分散液を得た。ついで、この微分
散液を厚さ4.5μmのポリエステルフィルム上にグラ
ビアコーティング法によって塗布し、85℃で乾燥させ
その塗布厚を5μmにして感熱転写型記録材を得た。Example 4 The hot-melt ink prepared in Example 1 was heated to 100°C, 3000 parts by weight of an aromatic mixed solvent (Pegasol R-100, manufactured by Mobil Oil) was added thereto, stirred, and allowed to cool. A fine dispersion of this ink was obtained. Next, this fine dispersion was applied onto a 4.5 μm thick polyester film by gravure coating and dried at 85° C. to give a coating thickness of 5 μm to obtain a heat-sensitive transfer type recording material.
比較例1
実施例1におイテ、EVAFLEX45XをNUCコボ
リマーMB−850 (エチレン−酢酸ビニル共重合体
、酢酸ビニル含有量: 22wt%、日本ユニカ一四l
ft)に替えた他は実施例1と同様になして感熱転写型
記録材を得た。Comparative Example 1 Same as Example 1, EVAFLEX 45X was used as NUC cobolimer MB-850 (ethylene-vinyl acetate copolymer, vinyl acetate content: 22 wt%, Nippon Unica 14l)
A thermal transfer type recording material was obtained in the same manner as in Example 1 except that ft) was used.
比較例2
カーボンブラック 120部パラフ
ィンワックス 100部(極性:無し
、155゜F、日本精蝋■製)キャンデリラワックス
470部(極性二大、野田ワックス課製
)
カルナウバワックス 150部EVA
FLEX45X 100部石油樹脂(エ
スコレッツ5380) 50部分散剤(ソルスパ
ース17000) 10部上記各成分を実施例1
と同様になして感熱転写型記録材を得た。Comparative Example 2 Carbon black 120 parts Paraffin wax 100 parts (Polarity: None, 155°F, manufactured by Nippon Seiro ■) Candelilla wax
470 parts (Polar Two, manufactured by Noda Wax Division) Carnauba wax 150 parts EVA
FLEX45X 100 parts Petroleum resin (Escolettes 5380) 50 parts Dispersant (Solspers 17000) 10 parts Each of the above components was added to Example 1
A thermal transfer type recording material was obtained in the same manner as above.
比較例3
カーボンブラック 120部パラフ
ィンワックス 360部(極性:無し
、155゜F、日本精蝋■製)マイクロクリスタリンワ
ックス 350部(極性:無し、H i M i
c 2 0 6 5、日本精蝋■製)
ソアレックスCH 150部分散
剤(ソルスパース17000) 20部上記各成
分を実施例1と同様の方法により熱溶融性インキを調整
したところ、三本ロールにより加温分散中に熱溶融性バ
インダーとエチレン−酢酸ビニル共重合体が分離してし
まい、インキを得ることが出来なかった。Comparative Example 3 Carbon black 120 parts Paraffin wax 360 parts (Polarity: None, 155°F, manufactured by Nippon Seiro ■) Microcrystalline wax 350 parts (Polarity: None, H i Mi
c2065, manufactured by Nippon Seiro ■) Solex CH 150 partial dispersant (Solspers 17000) 20 parts A hot-melt ink was prepared using the above ingredients in the same manner as in Example 1. During the temperature dispersion, the hot-melt binder and the ethylene-vinyl acetate copolymer separated, making it impossible to obtain an ink.
(発明の効果)
以上の実施例1〜4、比較例1〜3で得られた感熱転写
型記録材について記録紙としてはまなす紙(高平滑紙、
本州製紙■製)、上質紙(JISP3201).ゼロッ
クスL紙(乾式複写紙、富士ゼロックス■製)を使用し
て、ワープロ(JW一R55F.一東芝製)を用いてそ
れぞれの印字特性を調へた。(Effect of the invention) Regarding the thermal transfer recording materials obtained in Examples 1 to 4 and Comparative Examples 1 to 3, the recording paper used was hamanasu paper (highly smooth paper,
Made by Honshu Paper Industries, Ltd.), high quality paper (JISP3201). Using Xerox L paper (dry copy paper, manufactured by Fuji Xerox ■), the printing characteristics of each were investigated using a word processor (JW-R55F. manufactured by Toshiba).
結果を表1及び表2に示す。The results are shown in Tables 1 and 2.
※1分散状態:インキ中のエチレン−酢酸ビニル共重合
体の分散状態を目視で観察した。*1 Dispersion state: The dispersion state of the ethylene-vinyl acetate copolymer in the ink was visually observed.
0:良好,×:分散状態が不良
※2印字鮮明性:印字した文字の欠損部分の有無を観察
した。0: Good, ×: Poor dispersion state *2 Print clarity: The presence or absence of missing parts of printed characters was observed.
0:無,Δ:やや有,×:有
※3印字反射濃度:測定機としてサクラデンシトメータ
ーPDA− 65を使用し、測定した。数値は高いほど
濃度が高い
ことを示す。0: Absent, Δ: Slightly present, ×: Present *3 Print reflection density: Measured using Sakura Densitometer PDA-65 as a measuring device. The higher the value, the higher the concentration.
尚、比較例3は熱溶融性インキを得ることが出来ず、従
って印字試験が出来なかった。In addition, in Comparative Example 3, it was not possible to obtain hot-melt ink, and therefore the printing test could not be performed.
表1及び表2から明らかなように,本発明の感熱転写型
記録材によれば、サーマルプリンター専用紙はもちろん
のこと,一般紙(上質紙、乾式複写用紙)に対しても鮮
明な印字が可能となるものである。As is clear from Tables 1 and 2, the thermal transfer recording material of the present invention can print clearly not only on thermal printer paper but also on general paper (high-quality paper, dry copy paper). It is possible.
Claims (1)
くともなる感熱転写型記録材において、前記熱溶融性イ
ンキ層に、エチレン−酢酸ビニル共重合体の均一分散状
態を形成せしめることを特徴とする感熱転写型記録材。In a heat-sensitive transfer recording material comprising at least a base material and a heat-melt ink layer provided on the base material, forming a uniformly dispersed state of an ethylene-vinyl acetate copolymer in the heat-melt ink layer is provided. Features of thermal transfer recording material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013961A JPH03218892A (en) | 1990-01-24 | 1990-01-24 | Thermal transfer recording material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013961A JPH03218892A (en) | 1990-01-24 | 1990-01-24 | Thermal transfer recording material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03218892A true JPH03218892A (en) | 1991-09-26 |
Family
ID=11847810
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013961A Pending JPH03218892A (en) | 1990-01-24 | 1990-01-24 | Thermal transfer recording material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03218892A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0664224A2 (en) * | 1993-12-27 | 1995-07-26 | New Oji Paper Co., Ltd. | Heat-sensitive recording paper |
-
1990
- 1990-01-24 JP JP2013961A patent/JPH03218892A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0664224A2 (en) * | 1993-12-27 | 1995-07-26 | New Oji Paper Co., Ltd. | Heat-sensitive recording paper |
US5543382A (en) * | 1993-12-27 | 1996-08-06 | New Oji Paper Co., Ltd. | Heat-sensitive recording paper |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4777079A (en) | Image transfer type thermosensitive recording medium | |
JPS625887A (en) | Thermal transfer recording medium | |
US4783375A (en) | Heat-sensitive recording material | |
US4840837A (en) | Heat transfer medium | |
JPH03218892A (en) | Thermal transfer recording material | |
JPH041711B2 (en) | ||
US4965124A (en) | Thermal image transfer recording medium | |
JPS60184881A (en) | Thermal transfer recording medium | |
JPS63141786A (en) | Manufacture of heat transfer ink dative film | |
JP2571217B2 (en) | Thermal transfer recording medium | |
JPH02279386A (en) | Thermal transfer recording material | |
JPS62279984A (en) | Thermal transfer type recording material | |
JPS62218187A (en) | Thermal transfer recording medium | |
JPH01218888A (en) | Thermal transfer type recording material | |
JPS62220387A (en) | Thermal transfer recording medium | |
JPS61162395A (en) | Thermal transfer recording medium | |
JPS6179696A (en) | Thermal transfer recording medium | |
JPS6389383A (en) | Thermal transfer recording medium | |
JPH0585062A (en) | Production of thermal transfer recording material | |
JPS6351180A (en) | Thermal transfer recording medium | |
JPS6382782A (en) | Thermal transfer type recording material | |
JPS63268689A (en) | Thermal transfer type recording material | |
JPS6345091A (en) | Thermal transfer recording medium | |
JPS62242585A (en) | Thermal transfer recording medium | |
JPS62267188A (en) | Thermal transfer recording method |