JPS6141438B2 - - Google Patents
Info
- Publication number
- JPS6141438B2 JPS6141438B2 JP55075267A JP7526780A JPS6141438B2 JP S6141438 B2 JPS6141438 B2 JP S6141438B2 JP 55075267 A JP55075267 A JP 55075267A JP 7526780 A JP7526780 A JP 7526780A JP S6141438 B2 JPS6141438 B2 JP S6141438B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- information recording
- layer
- resin
- card
- 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
Links
- 239000002245 particle Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 17
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 239000000049 pigment Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 6
- 239000000314 lubricant Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000011342 resin composition Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 238000001454 recorded image Methods 0.000 claims description 4
- 230000001050 lubricating effect Effects 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000012463 white pigment Substances 0.000 claims 1
- 239000000976 ink Substances 0.000 description 41
- 238000000576 coating method Methods 0.000 description 28
- 239000011248 coating agent Substances 0.000 description 26
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000007788 liquid Substances 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 229920005749 polyurethane resin Polymers 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000020 Nitrocellulose Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000012461 cellulose resin Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000011086 glassine Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 description 1
- 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
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 229910000003 Lead carbonate Inorganic materials 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004698 Polyethylene 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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- TZHYBRCGYCPGBQ-UHFFFAOYSA-N [B].[N] Chemical compound [B].[N] TZHYBRCGYCPGBQ-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 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
- 229910052791 calcium Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000003077 polyols Chemical group 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- RCYJPSGNXVLIBO-UHFFFAOYSA-N sulfanylidenetitanium Chemical compound [S].[Ti] RCYJPSGNXVLIBO-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 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
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K19/00—Record carriers for use with machines and with at least a part designed to carry digital markings
- G06K19/02—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the selection of materials, e.g. to avoid wear during transport through the machine
- G06K19/022—Processes or apparatus therefor
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Theoretical Computer Science (AREA)
- Credit Cards Or The Like (AREA)
Description
【発明の詳細な説明】
本発明はカード基体上にインク吸収層、滑性層
を形成した後、感熱記録ヘツド等の加熱圧接によ
り熱転写リボンからインクを転写して画像記録す
る情報記録カードの製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to the production of an information recording card in which an ink absorbing layer and a lubricating layer are formed on a card substrate, and then ink is transferred from a thermal transfer ribbon by heat-pressure contact using a thermal recording head or the like to record an image. Regarding the method.
近年、記録、印字、マーキング等に関し、以下
に述べる要請が強く望まれる産業分野が非常に多
くなつてきている。即ち長期間苛酷な使用条件に
耐えなければならない、各種有価証券、カード証
明書、自動改札用定期券、ラベル等の情報記録カ
ードはその記録状報は耐摩耗性、耐候性、耐水
性、耐溶剤性、改ざん防止性、耐地汚れ防止性に
優れていなければならない、また情報記録方法と
してはコンピユータ等に記憶された情報で出力し
やすく、かつ機構および操作が簡単でなければな
らないなどである。 In recent years, there has been an increase in the number of industrial fields in which the following requirements regarding recording, printing, marking, etc. are strongly desired. In other words, information recording cards such as various securities, card certificates, commuter passes for automatic ticket gates, labels, etc. that must withstand harsh usage conditions for a long period of time have abrasion resistance, weather resistance, water resistance, and durability. It must be solvent-resistant, tamper-proof, stain-resistant, and the information recording method must be easy to output by storing information on a computer, etc., and the mechanism and operation must be simple. .
従来採用されてきた電子写真方法や静電記録方
法は一般に装置が複雑で、かつ大型になり価格も
高価となる欠点があり、また現像剤等の消耗材が
必要でありそれに伴ない保守管理が繁雑であると
いう欠点もあつた。この点を考えれば、感熱転写
記録方法は機構が簡単で消耗材が少なく、ランニ
ングコストが安価であることなどの理由により、
好ましい記録方法として評価され、紙を記録媒体
とするフアクシミリばかりでなく本発明の対象と
している情報記録カードの如き記録画像の耐久性
が要求される情報記録にも積極的に適用され始め
ている。 Conventionally used electrophotographic methods and electrostatic recording methods generally have the drawbacks of complex, large, and expensive equipment, and require consumables such as developers, which requires maintenance and management. It also had the disadvantage of being complicated. Considering this point, the thermal transfer recording method has a simple mechanism, fewer consumables, and low running costs.
It has been evaluated as a preferred recording method, and has begun to be actively applied not only to facsimiles using paper as a recording medium, but also to information recording that requires durability of recorded images, such as information recording cards, which are the object of the present invention.
しかしながらこれまでの適用例をみると耐久性
のある記録画像を得るために画像形成後さらに定
着手段を施して画像部のインクを剥れにくく強化
していた。これはインクがカード基体内に浸透せ
ずに表面に付着するだけであることを原因として
いる。従つてこのために定着手段として赤外線ヒ
ーター、フラツシユランプ、紫外線ランプを装備
して照射していたが、装置が繁雑になりランニン
グコストを上げる等の弊害を生じていた。 However, in the past examples of application, in order to obtain a durable recorded image, a fixing means was further applied after the image was formed to strengthen the ink in the image area so that it would not easily peel off. This is due to the fact that the ink does not penetrate into the card substrate but merely adheres to the surface. For this purpose, infrared heaters, flash lamps, and ultraviolet lamps have been installed as fixing means for irradiation, but these devices have become complicated and have disadvantages such as increased running costs.
本発明はこの点に鑑み鋭意研究の結果、インク
が充分に浸透でき、耐久性がありしかも地汚れの
ないカードとして実用性の高い情報記録カードの
製造方法を完成するに至り、ここに提供するもの
である。 In view of this, as a result of intensive research, the present invention has completed a highly practical method for producing an information recording card that allows sufficient penetration of ink, is durable, and has no background stains, and is provided herein. It is something.
本発明の記録媒体はブラスチツク、金属または
強じんな紙などを基体2とし、その表面にインク
の吸収、保持性を有するインク吸収層3、さらに
その上にインクを通過でき、かつ地汚れ防止をす
る滑性層4を設けた二層構成の記録層を設けたも
のである。この記録層の形成法としては塗液を塗
布する方法が最も実用的であるので以下にその塗
膜について詳しく述べる。 The recording medium of the present invention has a base 2 made of plastic, metal, or strong paper, and has an ink absorbing layer 3 on its surface that can absorb and retain ink, and further has an ink absorbing layer 3 on which ink can pass through and prevents scumming. A two-layer recording layer including a slippery layer 4 is provided. Since the most practical method for forming this recording layer is to apply a coating liquid, the coating film will be described in detail below.
まずインク吸収層の塗膜形成法について以下に
述べる。塗液の基本構成は粒子、この粒子を均一
に分散結着する樹脂およびこの樹脂を溶解する有
機溶剤とからなる。粒子の具体例としては通常用
いられる無機または有機白色顔料はすべて適用で
きる。 First, the method for forming the coating film of the ink absorbing layer will be described below. The basic composition of the coating liquid consists of particles, a resin that uniformly disperses and binds the particles, and an organic solvent that dissolves the resin. As specific examples of particles, all commonly used inorganic or organic white pigments can be used.
なお、着色した記録層を要求する場合は着色顔
料でもよい。一例を挙げれば、酸化チタン、炭酸
カルシウム、酸化亜鉛、酸化ケイ素、硫酸バリウ
ム、炭酸鉛、アルミナ、クレー等が使用できる。 Note that if a colored recording layer is required, colored pigments may be used. For example, titanium oxide, calcium carbonate, zinc oxide, silicon oxide, barium sulfate, lead carbonate, alumina, clay, etc. can be used.
一方、樹脂については、一般に塗料、インクに
用いられるバインダー用樹脂、例えばポリエステ
ル系、フエニル系、アルキツド系、アクリル系、
エポキシ系、ポリウレタン系、変性セルロース系
樹脂およびそれらの混合系等が使用できる。塗液
とするための混練分散は周知の方法で行なう。こ
の塗液をプラスチツクまたは金属等の耐久性のあ
る基体に塗布し、乾燥してインク吸収層を形成す
る。なお塗布については周知の塗布法を適用すれ
ば良い。この塗膜がインク吸収層としての特性を
得るために鋭意検討の結果、以下の要件が明らか
になつた。まず、顔料/樹脂の組成比は記録特性
(塗膜の多孔性に関連)、塗膜強度、基体との接着
性、耐摩耗性に対して顕著な効果を示すが、すべ
ての条件を満足するためには顔料/樹脂の組成比
は重量比で1/3〜4/1の範囲でなければならない。
なお、顔料の材料種、顔料の粒径、形状によつて
は上述の全範囲が適用できない場合があるが、い
ずれの材料構成でも共通している範囲は1/3〜4/1
である。次に顔料の粒径および粒度分布について
は多孔性、表面あらさを考慮して、粒径0.5〜5
μの範囲で粒度分布はできるだけせまいことがイ
ンク吸収層として良好な等性をもたらす。また塗
膜の厚さは10〜30μ程度が適当である。 On the other hand, regarding resins, binder resins commonly used in paints and inks, such as polyester, phenyl, alkyd, acrylic,
Epoxy resins, polyurethane resins, modified cellulose resins, and mixtures thereof can be used. Kneading and dispersion for preparing a coating liquid is performed by a well-known method. This coating solution is applied to a durable substrate such as plastic or metal and dried to form an ink absorbing layer. Note that a well-known coating method may be applied for coating. As a result of intensive studies, the following requirements were clarified in order for this coating film to have properties as an ink absorbing layer. First, the pigment/resin composition ratio has a significant effect on recording properties (related to the porosity of the coating film), coating strength, adhesion to the substrate, and abrasion resistance, and all conditions must be met. In order to achieve this, the pigment/resin composition ratio must be in the range of 1/3 to 4/1 by weight.
Note that the full range mentioned above may not be applicable depending on the pigment material type, pigment particle size, and shape, but the common range for all material configurations is 1/3 to 4/1.
It is. Next, regarding the particle size and particle size distribution of the pigment, the particle size is 0.5 to 5, taking into account porosity and surface roughness.
A particle size distribution as narrow as possible within the μ range provides good uniformity as an ink absorbing layer. Further, the appropriate thickness of the coating film is about 10 to 30 μm.
なお、塗膜の強度および耐溶剤性を向上させる
ために、バインダー樹脂を架橋型にすれば、なお
好ましい。例えば樹脂としてはポリオール基を有
するポリエステル系樹脂、ポリウレタン系樹脂を
含む樹脂を選び架橋剤としてイソシアネート基含
有化合物もしくは樹脂を加えてバインダー樹脂組
成とするなど周知の技術が適宜応用できる。 In addition, in order to improve the strength and solvent resistance of the coating film, it is more preferable to use a crosslinked binder resin. For example, well-known techniques can be applied as appropriate, such as selecting a polyester resin having a polyol group or a resin containing a polyurethane resin as the resin and adding an isocyanate group-containing compound or resin as a crosslinking agent to form a binder resin composition.
なお、基体が設けるべき記録層との接着力が弱
い場合に、記録層塗工前にあらかじめ接着力向上
のための下塗り層を設けることは当然の手法であ
る。 Incidentally, when the adhesive force between the substrate and the recording layer to be provided is weak, it is natural to provide an undercoat layer in advance to improve the adhesive force before coating the recording layer.
次に滑性層の塗膜形成法について以下に述べ
る。塗液の基本組成は白色または略白色の固体潤
滑剤粒子とこの粒子を均一に分散結着するバイン
ザー樹脂およびこの樹脂を溶解する有機溶剤から
成る。固体潤滑剤、粒子の具体例としては窒化ホ
ウ素、硫黄、雲母、タルク、ステアリン酸アルミ
ニウム、ステアリン酸カルシウム、硫化チタン、
硫化モリブデン、ポリエチレン、ポリアセター
ル、ポリ四フツ化エチレン等の白色もしくは略白
色の微粉末が好適である。一方樹脂については一
般に塗料、インクに用いられるバインダー用樹
脂、例えばポリエステル系、フエニル系、アルキ
ツド系、アクリル系、エポキシ系、ポリウレタン
系、変性セルロース系樹脂およびそれらの混合系
等が使用できる。塗液とするための混練分散は周
知の方法で行なう。この塗液を前述のインク吸収
層の上に塗布し、乾燥して滑性層を形成する。な
お塗布については周知の塗布法を適用すればよ
い。この滑性層が情報記録用インキを通過でき、
かつ地汚れを防止すべき滑性を有する特性を得る
ために検討した結果、さらに以下の要件が明らか
になつた。まず固体潤滑剤粒子/樹脂の組成比は
インク通過性、塗膜強度、インク吸収層との接着
性、耐摩耗性に対して大きく影響を及ぼすがすべ
ての条件を満足するためには固体潤滑剤/樹脂の
組成比は重量比で2/1〜20/1の範囲でなければな
らない。次に粒子の粒径については、あまり小さ
すぎるとインク通過性が減少し、あまり大きすぎ
ると表面あらさが大きくなりすぎ地汚れ防止効果
が減少するという結果から最適粒径範囲は0.5〜
10μとしなければならない。次の塗膜の厚さにつ
いてはあまり薄すぎると下のインク吸収層の表面
を充分に覆うことができず、あまり厚すぎるとイ
ンクの通過性が減少してしまうことを考え、最適
膜厚範囲に2〜10μとしなければならない。 Next, the method for forming the coating film of the slipping layer will be described below. The basic composition of the coating liquid consists of white or nearly white solid lubricant particles, a binder resin that uniformly disperses and binds the particles, and an organic solvent that dissolves the resin. Examples of solid lubricants and particles include boron nitride, sulfur, mica, talc, aluminum stearate, calcium stearate, titanium sulfide,
White or nearly white fine powders of molybdenum sulfide, polyethylene, polyacetal, polytetrafluoroethylene, etc. are suitable. On the other hand, as for the resin, binder resins generally used in paints and inks, such as polyester, phenyl, alkyd, acrylic, epoxy, polyurethane, modified cellulose resins, and mixtures thereof, can be used. Kneading and dispersion for preparing a coating liquid is performed by a well-known method. This coating liquid is applied onto the above-mentioned ink absorption layer and dried to form a slippery layer. Note that for coating, a well-known coating method may be applied. This slippery layer allows information recording ink to pass through,
As a result of studies to obtain properties with lubricity that should also prevent scumming, the following requirements were further clarified. First, the solid lubricant particle/resin composition ratio has a large effect on ink permeability, coating film strength, adhesion with the ink absorption layer, and abrasion resistance, but in order to satisfy all conditions, a solid lubricant must be used. The composition ratio of /resin must be in the range of 2/1 to 20/1 by weight. Next, regarding the particle size, if it is too small, the ink permeability will decrease, and if it is too large, the surface roughness will become too large and the scumming prevention effect will decrease, so the optimum particle size range is 0.5~
Must be 10μ. Regarding the thickness of the next coating film, we considered that if it is too thin, it will not be able to sufficiently cover the surface of the ink absorbing layer below, and if it is too thick, the ink permeability will decrease. The thickness should be 2 to 10μ.
本発明に適用する記録方法は感熱転写記録方法
であり、現在実用または開発されている記録装置
が適宜使用できる。記録装置については本発明の
主旨ではないので具体的な説明は省く、第2図に
本発明の感熱転写記録により情報記録カードを得
る概念図を示す。情報記録カード1は基体2にイ
ンク吸収層3、さらにその上に滑性層4が設けら
れている。 The recording method applied to the present invention is a thermal transfer recording method, and any recording device currently in use or developed can be used as appropriate. A detailed explanation of the recording device will be omitted since it is not the gist of the present invention, but FIG. 2 shows a conceptual diagram of obtaining an information recording card by thermal transfer recording of the present invention. The information recording card 1 includes a base 2, an ink absorption layer 3, and a slippery layer 4 provided thereon.
熱転写リボン5は、リボン基体6の上にインク
層7が設けられている。感熱記録ヘツド8と圧接
ローラ9との間にカード1と熱転写リボン5をイ
ンク層側をカード面に接するようにはさみ、加熱
圧接すると、加熱された部分のインクがカードに
転写されると同時に滑性層4を通過し、インク吸
収層3中に吸収保持される。インクの通過した部
分10およびインクの吸収保持された部分11が
画像部となる。 The thermal transfer ribbon 5 has an ink layer 7 provided on a ribbon base 6. The card 1 and the thermal transfer ribbon 5 are sandwiched between the thermal recording head 8 and the pressure roller 9 so that the ink layer side is in contact with the card surface, and when they are heated and pressed, the ink in the heated area is transferred to the card and at the same time it slides. The ink passes through the liquid layer 4 and is absorbed and retained in the ink absorbing layer 3. The portion 10 through which the ink has passed and the portion 11 where the ink has been absorbed and retained form an image portion.
ここで用いられる熱転写リボンのリボン基体は
10〜20μのセロハン、グラシン紙、ポリエステル
フイルムがよく、またインク層はインクのカード
内への吸収浸透性を考え50〜90℃で急激に軟化す
る特性を有するのが好ましい。そのためバインダ
ーとしてはワツクス、ロジン、低重合度のエポキ
シ樹脂、フエノール樹脂、石油樹脂、ブチラール
樹脂等ホツトメルト接着剤で通常使われているも
のから選ばれ、バインダー中に色料としてカーボ
ンブラツク、染料を10〜30重量%混合分散してイ
ンク層が形成できる。 The ribbon base of the thermal transfer ribbon used here is
Cellophane, glassine paper, or polyester film with a thickness of 10 to 20 μm is preferable, and the ink layer preferably has a property of rapidly softening at 50 to 90° C. in consideration of absorption and permeability of the ink into the card. Therefore, the binder is selected from those commonly used in hot melt adhesives such as wax, rosin, epoxy resin with a low degree of polymerization, phenol resin, petroleum resin, butyral resin, etc., and the binder contains carbon black and dye as colorants. An ink layer can be formed by mixing and dispersing ~30% by weight.
このようにして得られた情報記録カードはイン
クが記録と同時にカード内部に吸収保持されてし
まい、カードの表面には残つていないので、記録
後の定着手段が全く不要であり、かつ画像の耐摩
耗性、耐溶剤性、耐改ざん性はきわめて優れてい
るという特徴がある。 In the information recording card obtained in this way, the ink is absorbed and retained inside the card at the same time as recording, and does not remain on the surface of the card, so there is no need for any fixing means after recording, and the image remains unchanged. It is characterized by extremely excellent wear resistance, solvent resistance, and tamper resistance.
また本発明の滑性層は、カードの長期間の過酷
な使用、例えば磁気定期券のように自動改札機を
何回も通過させるような使い方に対しても、カー
ドの地汚れ、機械的な摩耗に対してきわめて優れ
た効果を発揮する。 In addition, the slippery layer of the present invention can withstand card smudges and mechanical damage, even when the card is used harshly over a long period of time, such as when a magnetic commuter pass is passed through an automatic ticket gate many times. Extremely effective against wear.
この情報記録カードに使用用塗に応じて所望の
絵柄、文字、地紋をあらかじめブレ印刷しておく
ことは当然できる。また、入力情報にて目視画像
のほかに磁気記録を併用する用途に対しては基体
の一部または磁気記録層を設けた情報記録カード
とすることもできる。 Of course, it is possible to print a desired picture, character, or background pattern on this information recording card in advance depending on the coating used. Furthermore, for applications in which magnetic recording is used in addition to visual images as input information, an information recording card may be provided with a part of the base or a magnetic recording layer.
次に実施例にて説明する。 Next, an example will be explained.
実施例 1
片面に磁気記録層をあらかじめ設けた白色ポリ
エステルフイルム(厚さ200μ)上に粉末シリカ
(水沢化学(株)製/平均粒径2μ)2部、(重量
比以下同)ポリウレタン樹脂(日本ポリウレタン
(株)製、ポリエステルポリオール/イソシアネ
ート系)4部、メチルエチルケトン8部、トルエ
ン2部からなる混合液をスクリユー撹拌式分散器
にて約20分撹拌して、均一分散した塗液をロール
コーター機にて塗布し、乾燥してインク吸収層を
形成した。膜厚は20μであつた。その上に、粉末
タルク平均粒径3μ)7部、ポリウレタン樹脂1
部、メチルエチルケトン8部、トルエン2部から
なる混合液をスクリユー撹拌式分散器にて、約10
分撹拌して均一分散した塗液をロールコーター機
にて塗布し、乾燥して膜厚4μの滑性層を形成し
た。これを所定の寸法に断載してカードとした。
熱転写リボンは20μのグラシン紙にカルナウバワ
ツクスとカーボンワツクス(重量比4/1)から
なるインク層を3.5μの厚さで形成したものであ
る。Example 1 2 parts of powdered silica (manufactured by Mizusawa Chemical Co., Ltd./average particle size 2μ) and (the same weight ratio) polyurethane resin (Japan A mixed solution consisting of 4 parts of polyester polyol/isocyanate (manufactured by Polyurethane Co., Ltd.), 8 parts of methyl ethyl ketone, and 2 parts of toluene was stirred for about 20 minutes in a screw-type disperser, and the uniformly dispersed coating liquid was applied to a roll coater. The ink absorbing layer was formed by coating and drying. The film thickness was 20μ. On top of that, 7 parts of powdered talc (average particle size 3μ), 1 part of polyurethane resin
About 10 parts of methyl ethyl ketone, 8 parts of toluene, and 2 parts of toluene were mixed in a screw-agitating disperser.
The coating solution was uniformly dispersed by stirring for several minutes and then applied using a roll coater, and dried to form a slippery layer with a thickness of 4 μm. This was cut into a predetermined size and made into a card.
The thermal transfer ribbon is made by forming an ink layer of carnauba wax and carbon wax (weight ratio 4/1) on 20μ glassine paper to a thickness of 3.5μ.
このカードと熱転写リボンを用いて感熱記録ヘ
ツドにて転写記録したところ、鮮明な浸透画像が
形成できた。記録直後熱定量は何ら施さないが、
このガード表面を指で強くこすつてもインクが消
えたり、流れたりすることはなかつた。 When transfer recording was performed using this card and a thermal transfer ribbon using a thermal recording head, a clear penetration image was formed. No thermal determination was performed immediately after recording, but
Even when I rubbed the surface of this guard vigorously with my finger, the ink did not disappear or run.
また、このカードを磁気情報読取ヘツド、およ
びその搬送系に2000回通風したが、カードが破損
したり、汚れたりすることは全くなく、記録画像
が消えるなどの劣化もなかつた。 Furthermore, although this card was ventilated 2000 times through the magnetic information reading head and its transport system, the card was not damaged or soiled at all, and there was no deterioration such as erasure of recorded images.
実施例 2
700μ厚の白色ポリ塩化ビニル製シート上に炭
酸カルシウム粉末(白石カルシウム(株)製)8
部、ポリエステル樹脂(東洋紡(株)1部、ニト
ロセルロース(ダイセル社製)0.2部、メチルエ
チルケトン15部、トルエン15部から成る混合液を
ボールミルにて約4時間混練した塗液をロールコ
ーター機にて塗布し、乾燥してインク吸収層を形
成した。さらにその上に、窒素ホウ素粉末(電気
化学工業(株)製)2部、ニトロセルロース1
部、イソプロピルアルコール15部、トルエン3部
からなる混合液をスクリユー撹拌式分散器にて約
1時間撹拌して、均一分散して塗液をグラビアコ
ーターにて塗布し、乾燥して膜厚3μの滑性層を
形成した。これを所定の寸法に断載してカードと
した。このカードと実施例1で用いた熱転写リボ
ンを用いて感熱記録ヘツドにて転写記録したとこ
ろ鮮明な浸透画像が形成された。記録直後熱定着
などは何ら施さなかつたが、このカード表面を指
で強くこすつてもインクが消えたり、流れたりす
ることはなかつた。Example 2 Calcium carbonate powder (manufactured by Shiroishi Calcium Co., Ltd.) 8 on a 700μ thick white polyvinyl chloride sheet
1 part of polyester resin (Toyobo Co., Ltd.), 0.2 parts of nitrocellulose (manufactured by Daicel), 15 parts of methyl ethyl ketone, and 15 parts of toluene were kneaded in a ball mill for about 4 hours, and then the coating liquid was mixed with a roll coater machine. It was coated and dried to form an ink absorbing layer.Furthermore, on top of that, 2 parts of nitrogen boron powder (manufactured by Denki Kagaku Kogyo Co., Ltd.) and 1 part of nitrocellulose were added.
15 parts of isopropyl alcohol, and 3 parts of toluene were stirred for about 1 hour using a screw-type stirrer disperser to uniformly disperse the coating liquid, which was then applied using a gravure coater and dried to form a film with a thickness of 3 μm. A slippery layer was formed. This was cut into a predetermined size and made into a card. When transfer recording was performed using this card and the thermal transfer ribbon used in Example 1 with a thermal recording head, a clear penetration image was formed. Although no heat fixing was performed immediately after recording, the ink did not disappear or run even when the surface of the card was strongly rubbed with a finger.
図面は本発明の実施例を示し、第1図は本発明
により作成される情報記録カードの構成図、第2
図は本発明を説明する概念図である。
1……情報記録カード、2……基本、3……イ
ンク吸収層、4……滑性層、5……熱転写リボ
ン、6……リボン基体、7……インク層、8……
感熱記録ヘツド、9……圧接ローラー。
The drawings show embodiments of the present invention, and FIG. 1 is a configuration diagram of an information recording card produced according to the present invention, and FIG.
The figure is a conceptual diagram explaining the present invention. DESCRIPTION OF SYMBOLS 1... Information recording card, 2... Basic, 3... Ink absorbing layer, 4... Lubricating layer, 5... Thermal transfer ribbon, 6... Ribbon base, 7... Ink layer, 8...
Heat-sensitive recording head, 9...pressure roller.
Claims (1)
持するインク吸収層を10〜30μの厚さで設けた
後、該インク吸収層の上に前記インクを通過させ
ることのできる滑性層を2〜10μの厚さで設け、
その後感熱記録ヘツド等の加熱圧接により、熱転
写リボンからインクを転写して記録画像を形成さ
せ、転写後の定着手段を施すことなく恒久画像を
得ることができる情報記録カードの製造方法。 2 前記インク吸収層を、粒径0.5〜5μの白色
もしくは略白色の顔料と該顔料を均一に分散結着
する樹脂から成り、顔料/樹脂の組成比を重量比
で1/3〜4/1であるように設けたことを特徴とする
特許請求の範囲第1項記載の情報記録カードの製
造方法。 3 前記滑性層を、粒径0.5〜10μの白色もしく
は略白色の固体潤滑剤粒子と該粒子を均一に分散
結着する樹脂から成り、粒子/樹脂の組成比が重
量比で2/1〜20/1であるように設けたことを特徴
とする特許請求の範囲第1項記載の情報記録カー
ドの製造方法。[Claims] 1. After providing an ink absorbing layer with a thickness of 10 to 30 μm for absorbing and retaining information recording ink on a card substrate, the ink can be passed over the ink absorbing layer. Provide a slippery layer with a thickness of 2 to 10μ,
A method for manufacturing an information recording card, in which ink is then transferred from a thermal transfer ribbon by heating and pressure using a thermal recording head or the like to form a recorded image, and a permanent image can be obtained without using any fixing means after transfer. 2. The ink absorbing layer is made of a white or nearly white pigment with a particle size of 0.5 to 5 μm and a resin that uniformly disperses and binds the pigment, and the pigment/resin composition ratio is 1/3 to 4/1 by weight. 2. A method for manufacturing an information recording card according to claim 1, wherein the information recording card is provided as follows. 3. The lubricating layer is made of white or nearly white solid lubricant particles with a particle size of 0.5 to 10μ and a resin that uniformly disperses and binds the particles, and the composition ratio of particles to resin is 2/1 to 2/1 by weight. 20/1. The method for manufacturing an information recording card according to claim 1, wherein the information recording card is provided so as to have a ratio of 20/1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7526780A JPS57785A (en) | 1980-06-03 | 1980-06-03 | Manufacture of information recording card |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7526780A JPS57785A (en) | 1980-06-03 | 1980-06-03 | Manufacture of information recording card |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57785A JPS57785A (en) | 1982-01-05 |
JPS6141438B2 true JPS6141438B2 (en) | 1986-09-16 |
Family
ID=13571269
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7526780A Granted JPS57785A (en) | 1980-06-03 | 1980-06-03 | Manufacture of information recording card |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57785A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5867497A (en) * | 1981-10-19 | 1983-04-22 | Toshiba Corp | Printer for recording medium |
JPS5964391A (en) * | 1982-10-04 | 1984-04-12 | Konishiroku Photo Ind Co Ltd | Heat sensitive transfer recording medium |
JPS5985792A (en) * | 1982-11-10 | 1984-05-17 | Matsushita Electric Ind Co Ltd | Image-receiving body for thermal transfer recording |
JPS60110489A (en) * | 1983-11-21 | 1985-06-15 | Toshiba Corp | Thermal transfer recording paper and thermal transfer recording apparatus using the same |
JPS6034898A (en) * | 1984-07-17 | 1985-02-22 | Dainippon Printing Co Ltd | Thermal transfer recording sheet |
JPS61188865U (en) * | 1985-05-17 | 1986-11-25 |
-
1980
- 1980-06-03 JP JP7526780A patent/JPS57785A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS57785A (en) | 1982-01-05 |
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