JPS6351180A - Thermal transfer recording medium - Google Patents
Thermal transfer recording mediumInfo
- Publication number
- JPS6351180A JPS6351180A JP61192769A JP19276986A JPS6351180A JP S6351180 A JPS6351180 A JP S6351180A JP 61192769 A JP61192769 A JP 61192769A JP 19276986 A JP19276986 A JP 19276986A JP S6351180 A JPS6351180 A JP S6351180A
- Authority
- JP
- Japan
- Prior art keywords
- transfer layer
- resin
- wax
- melting point
- softening point
- 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.)
- Granted
Links
- 229920005989 resin Polymers 0.000 claims abstract description 34
- 239000011347 resin Substances 0.000 claims abstract description 34
- 239000002245 particle Substances 0.000 claims abstract description 21
- 238000002844 melting Methods 0.000 claims abstract description 18
- 230000008018 melting Effects 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 8
- 239000000049 pigment Substances 0.000 claims abstract description 8
- 239000000975 dye Substances 0.000 claims description 5
- 239000001993 wax Substances 0.000 abstract description 17
- 238000005299 abrasion Methods 0.000 abstract description 10
- 239000011248 coating agent Substances 0.000 abstract description 6
- 238000000576 coating method Methods 0.000 abstract description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 4
- 229920006267 polyester film Polymers 0.000 abstract description 4
- -1 polyethylene Polymers 0.000 abstract description 4
- 238000007639 printing Methods 0.000 abstract description 4
- 229920000178 Acrylic resin Polymers 0.000 abstract description 3
- 239000004925 Acrylic resin Substances 0.000 abstract description 3
- 239000004698 Polyethylene Substances 0.000 abstract description 3
- 239000000113 methacrylic resin Substances 0.000 abstract description 3
- 229920000573 polyethylene Polymers 0.000 abstract description 3
- 239000004952 Polyamide Substances 0.000 abstract description 2
- 239000004203 carnauba wax Substances 0.000 abstract description 2
- 235000013869 carnauba wax Nutrition 0.000 abstract description 2
- 229920002647 polyamide Polymers 0.000 abstract description 2
- 239000004800 polyvinyl chloride Substances 0.000 abstract description 2
- 229920000915 polyvinyl chloride Polymers 0.000 abstract description 2
- 239000000976 ink Substances 0.000 description 9
- 239000000123 paper Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 241000411851 herbal medicine Species 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 230000008542 thermal sensitivity Effects 0.000 description 3
- NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- IYHIFXGFKVJNBB-UHFFFAOYSA-N 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonic acid Chemical compound C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S(O)(=O)=O IYHIFXGFKVJNBB-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 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
- 239000003086 colorant Substances 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
- 230000006866 deterioration Effects 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 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 1
- 230000005484 gravity Effects 0.000 description 1
- 235000010187 litholrubine BK Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000001454 recorded image Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000007651 thermal printing Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 238000010947 wet-dispersion method Methods 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
- B41M5/38228—Contact thermal transfer or sublimation processes characterised by the use of two or more ink layers
Abstract
Description
【発明の詳細な説明】
[技術分野]
本発明は、インク層の熱)容重性を利用して記録紙上に
熱転写記録をするための熱転写記録媒体に関するもので
、コンピューター、ワードプロセッサー等のプリンター
およびバーコードプリンター等にも応用できるものでお
る。Detailed Description of the Invention [Technical Field] The present invention relates to a thermal transfer recording medium for performing thermal transfer recording on recording paper by utilizing the heat/gravity of an ink layer, and is applicable to printers such as computers, word processors, etc. It can also be applied to code printers, etc.
[従来技術]
パラフィンワックスのような熱可融性性物質と染料、顔
料のような着色剤からなる転写層を支持体上に設けた熱
転写媒体が知られているが、パラフィンワックス類は機
械的強度が弱いために、転写画像の耐摩擦性が劣るとい
う欠点がおる。[Prior Art] A thermal transfer medium is known in which a transfer layer consisting of a heat-fusible substance such as paraffin wax and a coloring agent such as a dye or pigment is provided on a support. Since the strength is weak, there is a disadvantage that the abrasion resistance of the transferred image is poor.
この欠点を改善するために、熱可塑性樹脂を添加したり
、転写層をできるだけ薄くする方法がとられているが、
前者は樹脂成分が多くなると接着力が強くなって転写し
にくくなったり、熱感度が悪くなる問題がおり、後者は
転写画像の均一性が悪くなり、かつ、画像濃度が低下す
るという問題があった。In order to improve this drawback, methods have been taken such as adding thermoplastic resin or making the transfer layer as thin as possible.
The former has the problem that when the resin component increases, the adhesive force becomes strong, making it difficult to transfer, and the thermal sensitivity deteriorates, while the latter has the problem of poor uniformity of the transferred image and a decrease in image density. Ta.
[目 的]
本発明は従来技術の上記問題を解決し、記録紙上に高濃
度で均一性に優れた転写画像を1qることができ、しか
も、耐摩1察性に優れた転写画像が得られるような熱転
写記録媒体を提供することを目的としている。[Purpose] The present invention solves the above-mentioned problems of the prior art, makes it possible to produce 1 q of transferred images with high density and excellent uniformity on recording paper, and also provides transferred images with excellent abrasion resistance and perceptibility. The purpose is to provide such a thermal transfer recording medium.
[構 成]
上記目的を達成するための本発明の構成は、支持体上に
、下記(1)の構成を有する第1の転写層と下記(2)
の構成を有する第2の転写層とを順次有する熱転写記録
媒体でおる。[Structure] The structure of the present invention for achieving the above object includes a first transfer layer having the following structure (1) and the following (2) on a support.
This is a thermal transfer recording medium which sequentially has a second transfer layer having the following structure.
(1)融点または軟化点が75〜140℃の範囲にある
樹脂粒子と、融点または軟化点が70〜130 ℃の範
囲にあるワックスとを主成分とする第1の転写層。(1) A first transfer layer mainly composed of resin particles having a melting point or softening point in the range of 75 to 140°C and wax having a melting point or softening point in the range of 70 to 130°C.
(2)染料および/または顔料と、融点または軟化点が
60〜110℃の範囲にある樹脂粒子と、融点または軟
化点が70〜130℃の範囲にあるワックスとを主成分
とする第2の転写層。(2) A second material whose main components are dyes and/or pigments, resin particles having a melting point or softening point in the range of 60 to 110°C, and wax having a melting point or softening point in the range of 70 to 130°C. Transfer layer.
本発明の上記熱転写記録媒体の転写層を記録紙と重ね、
熱転写記録媒体の裏面からの熱印字によって記録紙上に
所望の画像が形成される。The transfer layer of the thermal transfer recording medium of the present invention is stacked on a recording paper,
A desired image is formed on the recording paper by thermal printing from the back side of the thermal transfer recording medium.
本発明にあける熱転写記録媒体の支持体どじでは従来公
知の種々のものが適宜使用できる。As the support for the thermal transfer recording medium according to the present invention, various conventionally known supports can be used as appropriate.
それ等を例示すると、ポリエステルフィルム、ポリアミ
ドフィルム、ポリ塩化ビニルフィルム、ポリエチレンフ
ィルム、ポリプロピレンフィルム、ポリイミドフィルム
、ボリザルフtンフィルム、ポリカーボネートフィルム
等のプラスチックフィルムあるいはコンデンサーペーパ
ー等がおる。Examples of these include plastic films such as polyester film, polyamide film, polyvinyl chloride film, polyethylene film, polypropylene film, polyimide film, borizalft film, and polycarbonate film, and condenser paper.
本発明に用いる染料、顔料としては印制インキ、塗料等
に用いられている無機及び有機の染顔料を用いることが
できる。具体例としてカーボンブラック、ジスアゾイエ
ロー、ブリリアントカーミン6B、レーキレッドC、フ
タロシアニンブルー、カヤセットブラックKR(日本生
薬)、オイルイエロー3G(オリエント化学)、カーV
セットレッドに−BE(日本生薬)、カヤセットブルー
KFL (日本生薬)等がある。As the dyes and pigments used in the present invention, inorganic and organic dyes and pigments used in printing inks, paints, etc. can be used. Specific examples include carbon black, Disazo Yellow, Brilliant Carmine 6B, Lake Red C, Phthalocyanine Blue, Kayaset Black KR (Nippon Herbal Medicine), Oil Yellow 3G (Orient Chemical), and Car V.
Set red includes -BE (Japanese Herbal Medicine), Kaya Set Blue KFL (Japanese Herbal Medicine), etc.
樹脂粒子に用いる樹脂としては融点もしくは軟化点(環
球法JIS K 2531) 60〜140℃の各種樹
脂が使用できる。As the resin used for the resin particles, various resins having a melting point or softening point (ring and ball method JIS K 2531) of 60 to 140°C can be used.
例えばアクリル樹脂、メタクリル樹脂、スチレン樹脂、
酢酸ビニル樹脂、塩化ビニル樹脂、塩化ビニリデン樹脂
、石油樹脂、ノボラック樹脂、オレフィン樹脂、ポリエ
ステル樹脂、ポリアセタール樹脂、エポキシプレポリマ
ー、おるいはこれらの共重合体等がおる。For example, acrylic resin, methacrylic resin, styrene resin,
Examples include vinyl acetate resin, vinyl chloride resin, vinylidene chloride resin, petroleum resin, novolac resin, olefin resin, polyester resin, polyacetal resin, epoxy prepolymer, or copolymer thereof.
また更に、樹脂粒子の融点もしくは軟化点を調整するた
めに可塑剤を必要に応じて使用することもできる。Furthermore, a plasticizer can be used as necessary to adjust the melting point or softening point of the resin particles.
例えば、ジメチルフタレート、ジエチルフタレート、ジ
ブチルフタレート、ジオクチルフタレート、ジシクロヘ
キシルフタレート、ジー2−エチルへキシルアジペ−1
へ、ジエチレングリコールジベンゾエート、ブチルステ
アレート、トリフェニルフォスフェート等でおる。For example, dimethyl phthalate, diethyl phthalate, dibutyl phthalate, dioctyl phthalate, dicyclohexyl phthalate, di-2-ethylhexyl adip-1
and diethylene glycol dibenzoate, butyl stearate, triphenyl phosphate, etc.
第1の転写層に用いる樹脂粒子の融点もしくは軟化点が
75°Cより低いと、転写画像の高温環境(50〜60
℃)における耐摩擦性が悪くなり、140°Cより高い
と熱転写記録の際のエネルギーだけでは充分定着されに
くくなり、耐摩擦性が劣る、さもなくば、高エネルギー
記録を必要とするために、記録速度が遅くなったり、サ
ーマルヘッドの寿命が短くなる等の問題が起こる。If the melting point or softening point of the resin particles used for the first transfer layer is lower than 75°C, the transfer image will be exposed to a high temperature environment (50 to 60°C).
If the temperature is higher than 140°C, it becomes difficult to fix the film sufficiently with energy alone during thermal transfer recording, resulting in poor abrasion resistance. Otherwise, high energy recording is required. Problems arise such as the recording speed becomes slower and the life of the thermal head becomes shorter.
また、第2の転写層に用いる樹脂粒子の融点または軟化
点が60°Cより低いと熱転写記録媒体を保管している
間に転写層がブロッキング等を起し、110℃より高い
と転写画像の均一性が悪くなるので好ましくない。Furthermore, if the melting point or softening point of the resin particles used for the second transfer layer is lower than 60°C, the transfer layer may cause blocking while the thermal transfer recording medium is stored, and if it is higher than 110°C, the transferred image This is not preferable because the uniformity deteriorates.
本発明に用いる樹脂粒子は、各種樹脂を微粒子化(乳化
重合、サンドミル等による湿式分散法、ジェットミル等
による乾式分散法等が必る)して1qることができる。The resin particles used in the present invention can be made into 1q by micronizing various resins (requires emulsion polymerization, wet dispersion using a sand mill, etc., dry dispersion using a jet mill, etc.).
樹脂粒子の平均径は0.1〜5μm、特に1〜3μm程
度が好ましい。0.1μm未満では転写の際にスティッ
キングが発生し易くなり、5μmを越えると熱感度、解
像性が悪くなるので好ましくない。The average diameter of the resin particles is preferably about 0.1 to 5 μm, particularly about 1 to 3 μm. If it is less than 0.1 μm, sticking will easily occur during transfer, and if it exceeds 5 μm, thermal sensitivity and resolution will deteriorate, which is not preferable.
本発明に用いるワックスとしては、融点または軟化点が
70〜130 ℃のものが適当である。The wax used in the present invention is suitably one having a melting point or softening point of 70 to 130°C.
このワックスの融点もしくは軟化点が70℃よりも低い
と、印加された熱エネルギーが該ワックスを溶融するた
めに消費されるために、樹脂を軟化するエネルギーが不
足する。そのためワックスのみが優先的に転写し、転写
層の転写が不充分となり転写画像のカスレを生じ鮮明性
が低下する。また、130℃よりも高いと転写のために
高い熱エネルギーを必要とする。If the melting point or softening point of this wax is lower than 70° C., the applied thermal energy is consumed to melt the wax, resulting in insufficient energy to soften the resin. Therefore, only the wax is preferentially transferred, and the transfer of the transfer layer becomes insufficient, causing blurring of the transferred image and deterioration of sharpness. Further, if the temperature is higher than 130° C., high thermal energy is required for transfer.
また、このようなワックスの針入度は1以下が好ましく
、針入度が1より大きいと記録画像の耐ひつかき性が低
下する。Further, the penetration degree of such wax is preferably 1 or less, and if the penetration degree is greater than 1, the scratch resistance of the recorded image will decrease.
具体的には、カルナバワックス、ポリエチレンワックス
、フィンシャートロプシュワックス、モンクンワックス
誘導体、硬化ひまし油等が挙げられる。Specific examples include carnauba wax, polyethylene wax, Finscher-Tropsch wax, monk wax derivatives, and hydrogenated castor oil.
これらのワックスの使用mは熱感度、熱転写画像の耐摩
擦性に影響する。ワックスの使用割合は、転写層の全固
形分付着量の10〜70重量%が好ましく、10重量%
未満では均一な転写画像が得られず、70重最%を越え
ると耐摩擦性が悪くなり、好ましくない。The use of these waxes affects the thermal sensitivity and abrasion resistance of thermally transferred images. The proportion of wax used is preferably 10 to 70% by weight of the total solid content of the transfer layer, and 10% by weight.
If it is less than 70% by weight, a uniform transferred image cannot be obtained, and if it exceeds 70% by weight, the abrasion resistance deteriorates, which is not preferable.
その信奉発明の転写層にはワックス以外のバインダーを
適宜用いることが出来るが、その使用■は転写を阻害し
ない最少限度にすべきであり、転写層の全固形分付着量
の0〜25重量%程度である。これらのバインダーとし
ては開用のものを用いることが出来、例えばポリビニル
アルコール、メトキシセルロース、ヒドロキシエヂルセ
ルロース、カルボキシメヂルセルロース、ポリビニルピ
ロリドン、ポリアクリルアミド、デンプン、ゼラチン、
アクリル樹脂、メタクリル樹脂、酢酸ビニル樹脂、塩化
ビニル樹脂、塩化ビニリデン(H脂、オレフィン樹脂、
ポリエステル樹脂、あるいはこれらの共重合体等である
。Binder other than wax can be used as appropriate in the transfer layer of the invention, but its use should be kept to the minimum limit that does not inhibit the transfer, and should be 0 to 25% by weight of the total solid content of the transfer layer. That's about it. As these binders, conventional binders can be used, such as polyvinyl alcohol, methoxycellulose, hydroxyedylcellulose, carboxymethylcellulose, polyvinylpyrrolidone, polyacrylamide, starch, gelatin,
Acrylic resin, methacrylic resin, vinyl acetate resin, vinyl chloride resin, vinylidene chloride (H fat, olefin resin,
These include polyester resins or copolymers thereof.
本発明の熱転写記録媒体と共に用いる記録紙としては普
通紙、合成紙、プラスチックフィルム等を適宜用いるこ
とができる。As the recording paper used with the thermal transfer recording medium of the present invention, plain paper, synthetic paper, plastic film, etc. can be used as appropriate.
本発明の熱転写記録媒体は、前記の転写層形成成分を水
または樹脂粒子を溶解しない溶媒と共に混合し、攪拌機
、ボールミル、アトライター等の分散手段によって樹脂
粒子の平均粒径が0.1〜5μmになるように分散せし
めて、これを支持体上に全固形分付着量が1〜10 g
/m2になるように塗布し、樹脂粒子を融着せしめない
ように、樹脂粒子の軟化点以下の温度で乾燥することに
よって作製することができる。The thermal transfer recording medium of the present invention is produced by mixing the above-mentioned transfer layer forming components with water or a solvent that does not dissolve the resin particles, and using a dispersing means such as a stirrer, a ball mill, an attritor, etc., the average particle size of the resin particles is reduced to 0.1 to 5 μm. Disperse it on the support so that the total solid content is 1 to 10 g.
/m2 and drying at a temperature below the softening point of the resin particles so as not to fuse the resin particles.
[実施例]
次に本発明を実施例によりさらに詳細に説明する。なあ
、以下において示す1部」およびF%」はいずれも張徂
基卓である。[Example] Next, the present invention will be explained in more detail with reference to Examples. By the way, both ``Part 1'' and ``F%'' shown below are Zhang Chejizhuo.
1、カーボンブラック分散液の作製
カーボンブラック 20部界面活性剤
2部水
78部上記組成の材料をボールミルで2
4時間分散した。1. Preparation of carbon black dispersion Carbon black 20 parts Surfactant
2 parts water
78 parts of the material with the above composition in a ball mill
Dispersed for 4 hours.
2、樹脂粒子分散液の作製
第1表
上記第1表に記載の材料をボールミルで24時間分散し
、平均粒径2μの樹脂粒子の分散液G(,7た。2. Preparation of Resin Particle Dispersion Table 1 The materials listed in Table 1 above were dispersed in a ball mill for 24 hours to obtain a dispersion G of resin particles with an average particle size of 2 μm.
実施例1〜6
第1転写層用塗布液の調製
上記第2表に記載の組成物を攪拌機で均一にン昆合した
。Examples 1 to 6 Preparation of coating liquid for first transfer layer The compositions listed in Table 2 above were mixed uniformly using a stirrer.
第2転写層用塗布液の調製 第3表 上記第3表に記載の組成物を攪拌機で均一に混合した。Preparation of coating liquid for second transfer layer Table 3 The compositions listed in Table 3 above were mixed uniformly using a stirrer.
熱転写記録媒体の作製
上記第1転写層用塗布液(第2表)を6μm厚のポリエ
ステルフィルム上に乾燥後の付Wffiが2g/m2に
なるようにワイヤーバーを用いて塗布し、温PA(40
〜50℃)乾燥した。Preparation of thermal transfer recording medium The above coating liquid for the first transfer layer (Table 2) was applied onto a 6 μm thick polyester film using a wire bar so that the applied Wffi after drying was 2 g/m2, and then warm PA ( 40
~50°C).
次いで第2転写層用塗布液(第3表)を第1転写層上に
乾燥後の付着量が2g/m 2になるように同様に塗布
し乾燥し、第1、第2転写層がそれぞれ第4表に記載の
組合せで必る熱転写記録媒体を作製した。Next, the coating liquid for the second transfer layer (Table 3) was similarly applied onto the first transfer layer so that the amount of adhesion after drying was 2 g/m2, and dried, so that the first and second transfer layers were coated, respectively. A thermal transfer recording medium was prepared using the combinations listed in Table 4.
第4表
比較例1
塗布!N0.2を乾燥後の付着量が4g/m 2になる
ように6μ厚ポリエステルフイルムに塗布、乾燥し熱転
写記録媒体を作製した。Table 4 Comparative Example 1 Application! N0.2 was applied onto a 6 μm thick polyester film so that the amount of adhesion after drying was 4 g/m 2 and dried to produce a thermal transfer recording medium.
比較例2
塗布液N0.6を比較例1と同様にして熱転写記録媒体
を作製した。Comparative Example 2 A thermal transfer recording medium was prepared using the same coating liquid N0.6 as in Comparative Example 1.
比較例3.4 第5表 実施例1〜6と同様の方法で熱転写記録媒体を1dた。Comparative example 3.4 Table 5 A thermal transfer recording medium of 1 d was prepared in the same manner as in Examples 1 to 6.
以上のようにして作製した熱転写記録媒体を、その転写
層を上質紙表面に密着させて熱転写プリンターを用いて
0.5mJ /datのエネルギーを与えて印字した。The thermal transfer recording medium produced as described above was printed using a thermal transfer printer by applying an energy of 0.5 mJ/dat with the transfer layer brought into close contact with the surface of high-quality paper.
更に、印字画像の耐摩擦性を調べるために、ラボテスタ
ー(東洋装機製)を用いてダンボールに対する耐摩擦性
(¥温20.50°C)を試験した。Furthermore, in order to examine the abrasion resistance of the printed image, the abrasion resistance (temperature: 20.50°C) against cardboard was tested using a lab tester (manufactured by Toyosoki Co., Ltd.).
その結果は下記第6表の通りであった。The results were as shown in Table 6 below.
第6表
面像′a度二へり印字部の反射濃度(マクベス反射濃度
計)
均−性二ペタ印字部のボイド(インクが転写していない
個所)の有無
良・・・ボイドなし
ヤヤ悪い・・・ボイド少しあり
悪・・・ボイドが多い
耐摩原性:摩擦回数100往復
荷重 100g/cm2
良・・・変化なし
やや悪・・・印字部のインクが少し取られ非印字に少し
付く
悪・・・印字部のインクが多く取ら
れ非印字部にかなり付く
耐ひっかき性:バーコード読み取り用ペンスキャナーで
転写画像を擦り、印字部のイ
ンクの取られ具合をみた
良・・・変化なし
悪・・・印字部のインクが取られ、
非印字部に付く
[効 果]
以上説明したように、本発明の熱転写記録媒体を用いる
ことによって、高濃度で均一性が良く、耐摩擦性にすぐ
れた転写画像が1昇られる。6th surface image 'a Reflection density of the two-edge printing area (Macbeth reflection densitometer) Uniformity: presence or absence of voids (areas where ink is not transferred) in the two-peta printing area...no voids, very bad...・Some voids, bad: Many voids Abrasion resistance: 100 friction cycles, 100g/cm2 Good: No change, slightly bad: A little ink is removed from the printed area, and a little bit sticks to the non-printed areas.・Scratch resistance: A lot of ink is removed from the printed area and a lot of ink is attached to the non-printed area: I rubbed the transferred image with a barcode reading pen scanner and looked at how much ink was removed from the printed area...No change, bad...・Ink is removed from the printed area and attached to the non-printed area [Effect] As explained above, by using the thermal transfer recording medium of the present invention, the ink can be transferred with high density, good uniformity, and excellent abrasion resistance. The image is incremented by 1.
Claims (1)
下記(2)の構成を有する第2の転写層とを順次有する
ことを特徴とする熱転写記録媒体。 (1)融点または軟化点が75〜140℃の範囲にある
樹脂粒子と、融点または軟化点が70〜130℃の範囲
にあるワックスとを主成分とする第1の転写層。 (2)染料および/または顔料と、融点または軟化点が
60〜110℃の範囲にある樹脂粒子と、融点または軟
化点が70〜130℃の範囲にあるワックスとを主成分
とする第2の転写層。[Scope of Claims] A thermal transfer recording medium characterized by having, on a support, a first transfer layer having the following configuration (1) and a second transfer layer having the following configuration (2) in sequence. . (1) A first transfer layer whose main components are resin particles whose melting point or softening point is in the range of 75 to 140°C and wax whose melting point or softening point is in the range of 70 to 130°C. (2) A second material whose main components are dyes and/or pigments, resin particles having a melting point or softening point in the range of 60 to 110°C, and wax having a melting point or softening point in the range of 70 to 130°C. Transfer layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61192769A JP2571218B2 (en) | 1986-08-20 | 1986-08-20 | Thermal transfer recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61192769A JP2571218B2 (en) | 1986-08-20 | 1986-08-20 | Thermal transfer recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6351180A true JPS6351180A (en) | 1988-03-04 |
JP2571218B2 JP2571218B2 (en) | 1997-01-16 |
Family
ID=16296726
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61192769A Expired - Lifetime JP2571218B2 (en) | 1986-08-20 | 1986-08-20 | Thermal transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2571218B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06190332A (en) * | 1992-12-25 | 1994-07-12 | Kansai Paint Co Ltd | Method for finishing coating |
US5348997A (en) * | 1992-04-24 | 1994-09-20 | Mitsubishi Yuka Badische Co., Ltd. | Crosslinking aqueous pigment dispersion |
US5432229A (en) * | 1993-03-26 | 1995-07-11 | Mitsubishi Yuka Badische Co., Ltd. | Aqueous crosslinkable resin composition |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5410495A (en) * | 1977-06-23 | 1979-01-26 | Mitsubishi Electric Corp | Laser working apparatus with reflector |
JPS57199472U (en) * | 1981-06-15 | 1982-12-18 | ||
JPS58219086A (en) * | 1982-06-15 | 1983-12-20 | Konishiroku Photo Ind Co Ltd | Heat-sensitive transfer recording medium |
JPS60102959U (en) * | 1983-12-19 | 1985-07-13 | 凸版印刷株式会社 | Donor sheet for thermal transfer |
JPS60236790A (en) * | 1984-05-10 | 1985-11-25 | Toshiba Corp | Thermal transfer material |
JPS6178692A (en) * | 1984-09-26 | 1986-04-22 | Mitsubishi Paper Mills Ltd | Thermal transfer material |
JPS6221586A (en) * | 1985-07-23 | 1987-01-29 | Canon Inc | Thermal transfer material and production thereof |
-
1986
- 1986-08-20 JP JP61192769A patent/JP2571218B2/en not_active Expired - Lifetime
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5410495A (en) * | 1977-06-23 | 1979-01-26 | Mitsubishi Electric Corp | Laser working apparatus with reflector |
JPS57199472U (en) * | 1981-06-15 | 1982-12-18 | ||
JPS58219086A (en) * | 1982-06-15 | 1983-12-20 | Konishiroku Photo Ind Co Ltd | Heat-sensitive transfer recording medium |
JPS60102959U (en) * | 1983-12-19 | 1985-07-13 | 凸版印刷株式会社 | Donor sheet for thermal transfer |
JPS60236790A (en) * | 1984-05-10 | 1985-11-25 | Toshiba Corp | Thermal transfer material |
JPS6178692A (en) * | 1984-09-26 | 1986-04-22 | Mitsubishi Paper Mills Ltd | Thermal transfer material |
JPS6221586A (en) * | 1985-07-23 | 1987-01-29 | Canon Inc | Thermal transfer material and production thereof |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5348997A (en) * | 1992-04-24 | 1994-09-20 | Mitsubishi Yuka Badische Co., Ltd. | Crosslinking aqueous pigment dispersion |
JPH06190332A (en) * | 1992-12-25 | 1994-07-12 | Kansai Paint Co Ltd | Method for finishing coating |
JP2610085B2 (en) * | 1992-12-25 | 1997-05-14 | 関西ペイント株式会社 | Paint finishing method |
US5432229A (en) * | 1993-03-26 | 1995-07-11 | Mitsubishi Yuka Badische Co., Ltd. | Aqueous crosslinkable resin composition |
Also Published As
Publication number | Publication date |
---|---|
JP2571218B2 (en) | 1997-01-16 |
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