JPS6315657B2 - - Google Patents
Info
- Publication number
- JPS6315657B2 JPS6315657B2 JP52032838A JP3283877A JPS6315657B2 JP S6315657 B2 JPS6315657 B2 JP S6315657B2 JP 52032838 A JP52032838 A JP 52032838A JP 3283877 A JP3283877 A JP 3283877A JP S6315657 B2 JPS6315657 B2 JP S6315657B2
- Authority
- JP
- Japan
- Prior art keywords
- layer
- magnetic
- coating layer
- thickness
- microns
- 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
- 239000010410 layer Substances 0.000 claims description 72
- 239000011247 coating layer Substances 0.000 claims description 30
- 239000011253 protective coating Substances 0.000 claims description 20
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 239000012790 adhesive layer Substances 0.000 claims description 14
- 238000007740 vapor deposition Methods 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 7
- 239000002131 composite material Substances 0.000 claims description 2
- 239000010408 film Substances 0.000 description 26
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000003973 paint Substances 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000000976 ink Substances 0.000 description 7
- 239000002184 metal Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000003086 colorant Substances 0.000 description 5
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000000696 magnetic material Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000012461 cellulose resin Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000005347 demagnetization Effects 0.000 description 2
- 238000003487 electrochemical reaction Methods 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 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
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000459 Nitrile rubber Polymers 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
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229940090961 chromium dioxide Drugs 0.000 description 1
- IAQWMWUKBQPOIY-UHFFFAOYSA-N chromium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Cr+4] IAQWMWUKBQPOIY-UHFFFAOYSA-N 0.000 description 1
- AYTAKQFHWFYBMA-UHFFFAOYSA-N chromium(IV) oxide Inorganic materials O=[Cr]=O AYTAKQFHWFYBMA-UHFFFAOYSA-N 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 239000011104 metalized film Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Magnetic Record Carriers (AREA)
Description
本発明は磁気貼合型記録体に関し、特に磁性体
色とは異なる種々の色彩が賦与されるとともにス
ペーシングロスが極めて小さく入出力特性に優れ
た磁気記録層を形成し得る磁気貼合型記録体に関
する。
支持体の表面に磁気塗膜層を設け裏面に接着剤
層を設けた磁気貼合型記録体を用いて、預金通
帳、クレジツトカード、コンピユーターの入出力
媒体等に磁気記録層を形成することは最近では広
く行なわれているが、これに伴ない、美感上の必
要性から、磁気記録層に磁性体特有の黒乃至茶褐
色の色彩とは異なる色彩を賦与したいとする要望
が次第に高まつてきている。近時これに呼応し
て、預金通帳などに使用される磁気貼合型記録体
として、磁気塗膜層上に直接着色塗膜層を設けた
ものが提供されているが、この種の磁気貼合型記
録体では着色塗膜層の隠蔽力不足のために貼合さ
れた磁気記録層の色は相当汚れた色にならざるを
得ないし、また、着色塗膜層に充分な隠蔽力を持
たせるためにその塗膜厚を厚くすると、磁気記録
層の入出力特性が低下し、検出ミスを起し易い欠
点がある。
本発明は斯る点に鑑みてなされたものであり、
従つて、本発明の目的は磁性体色とは異なる種々
の色彩が賦与され、その色彩が長期間に亘り全く
変化がなく美観上極めて優れた、しかもスペーシ
ングロスが極めて小さく入出力特性に優れた磁気
記録層を形成し得る磁気貼合型記録体を提供する
ことにある。
本発明者等は、鋭意研究の結果、基本的には磁
気塗膜層上にSn蒸着膜層を設け更にこの上にSn
蒸着膜層を保護する着色された保護塗膜層を設け
ることによつて上記目的を達成し得ることを見い
出した。即ち、Sn蒸着塗膜層は極めて薄膜であ
るにもかかわらず隠蔽力が極めて大であるため
に、これによつて磁気塗膜層の色を完全に隠蔽す
ることが可能であり、従つて、この上に着色され
た保護塗膜層を設けるときは、その塗膜厚を相当
薄くしてもこれによる着色は有効である。よつ
て、斯る基本的構成を有する磁気貼合型記録体
は、所望の色が賦与されるとともにスペーシング
ロスが極めて小さく、入出力特性に優れた磁気記
録層を形成し得る。また、上記の着色された保護
塗膜層に替えて透明な保護塗膜層を設けた磁気貼
合型記録体は、金属蒸着膜層の金属色がそのまま
現出するとともに入出力特性に優れた興味ある磁
気記録層を形成し得ることも見い出された。
本発明は斯る知見に基いて完成されたものであ
つて、本発明によれば、シール状またはフイルム
状の支持体1の表面に磁気塗膜層2、Sn蒸着膜
層3および保護塗膜層4が順次積層状に設けられ
るとともに支持体1の裏面に接着剤層5が設けら
れた磁気貼合型記録体が提供される。
支持体1としてはプラスチツクシートまたはフ
イルムが使用され、特にポリエステル、ポリカー
ボネート等のシートまたはフイルムが好適であ
る。支持体1の厚さには特に制限はないが、通常
20〜100ミクロン程度のものが一般的に使用され
る。
支持体1の表面には磁気塗膜層2が設けられる
が、磁気塗膜層2を形成するには例えばγ―酸化
鉄、Co―ドーブ酸化鉄、二酸化クロム、フエラ
イト等の磁性体微粒子を含有する磁気塗料をロー
ルコーター等によつて支持体1の表面に塗布すれ
ばよい。また、その膜厚は記臆容量等を考慮して
適宜定めればよいのであつて、通常5〜20ミクロ
ンとすればよい。磁気塗料としては特に制限はな
く、例えばセルロース樹脂、塩ビ樹脂、塩ビ―酢
ビ共重合体、ウレタン樹脂、エポキシ樹脂、ポリ
エステル樹脂、スチレンブタジエンラバー等をバ
インダー成分とし、好適にはこれらの樹脂に適当
な硬化剤を添加し、更に必要に応じて各種助剤を
添加して成る磁気塗料を使用すればよい。
磁気塗膜層2上にはSn蒸着膜層3が設けられ
るが、磁気塗膜層2の磁気特性を乱さず磁気塗膜
層の色を隠蔽するという点からのみ考慮するなら
ば、Sn蒸着膜層3に代えてMg.Al.Zn.Pt.Au.Ag
等による蒸着膜層を使用することもできる。しか
し、これら金属による蒸着膜層は磁気塗膜層と接
触していると、長期間保存中に、金属蒸着膜層中
の前記金属と磁気塗膜層中に含有されるγ―酸化
鉄、フエライト等の磁性体微粒子との間に指脂、
湿気等に起因すると考えられる電気化学的反応が
起り、その結果金属蒸着膜層上に見苦しい黒色状
斑点がしばしば現われる。しかしながら、蒸着金
属としてSnを使用するときは斯る斑点の発生は
全く認められない。Sn蒸着膜層3を形成するに
は公知の金属蒸着機を用いればよい。また、その
膜厚は磁気塗膜層2を完全に隠蔽するに足る最小
の厚さでよく、例えば100〜1000A゜とすればよ
い。
磁気塗膜層2とSn蒸着膜層3との層間密着性
が不充分である場合には、これを補強するため
に、必要に応じて磁気塗膜層2とSn蒸着膜層3
の間にアンカー剤層6を介在させればよい。アン
カー剤としては例えば塩ビ―酢ビ共重合体系、エ
ポキシ樹脂系、ポリアミド樹脂系等の市販アンカ
ー剤やポリビニルブチラールー重クロム酸カリー
リン酸系ウオツシユプライマーを使用できる。ア
ンカー剤層6を形成するには、磁気塗膜層2上に
上記アンカー剤をロールコーターによつて膜厚
0.01〜1.0ミクロンとなるように塗布すればよい。
Sn蒸着膜層3上には保護塗膜層4が設けられ
るが、保護塗膜層4はSn蒸着膜層3を保護し、
必要に応じてこれを着色するためのものであり、
透明もしくは不透明または着色もしくは無着色の
別を問わない。即ち、保護塗膜層4は透明層また
は着色層の何れの単層であつてもよいし、またそ
れらの複合層であつても一向に差支えない。保護
塗膜層4を形成するには、Sn蒸着膜層3上にロ
ールコーター、グラビヤ印刷機等を用いて透明も
しくは着色された塗料またはインキで塗装または
印刷を施す。斯る透明もしくは着色された塗料ま
たはインキとしては、例えばセルロースアセテー
トブチレート、ニトロセルロースの如きセルロー
ス系樹脂、アクリル樹脂、ブチラール樹脂、塩ビ
―酢ビ系共重合体、ポリエステル樹脂、アルキツ
ド樹脂、ウレタン樹脂、エポキシ樹脂、ポリアミ
ド樹脂、エチレン―酢ビ共重合体、シリコン樹脂
等をバインダー成分とし、必要に応じてこれらの
樹脂に着色剤、硬化剤、滑剤その他の助剤を添加
してなる熱可塑性または熱硬化性の塗料またはイ
ンキが使用できる。
保護塗膜層4の膜厚は入出力特性から言えば薄
いほど良いが、強度、耐久性等とのバランスを考
慮すると0.1〜5ミクロンの範囲とすることが望
ましい。
Sn蒸着膜層3と保護塗膜層4との層間密着性
が不充分である場合には、これを補強するため
に、必要に応じてSn蒸着膜層3と保護塗膜層4
との間にアンカー剤層7を介在させればよく、そ
のアンカー剤としては前記同様のアンカー剤を使
用すればよい。
一方、支持体1の裏面には接着剤層5が設けら
れるが、接着剤層5としては感熱性接着剤層、感
圧性接着剤層の何れでもよい。接着剤層5を形成
するには、例えば塩化ビニール樹脂、酢酸ビニー
ル樹脂、塩ビ―酢ビ共重合体、ウレタン樹脂、ア
クリロニトリルブタジエン樹脂、ポリエステル樹
脂、セルロース樹脂、塩ビ―塩化ビニリデン共重
合体、エポキシ樹脂、天然ゴム、ロジン等に必要
に応じて可塑剤、助剤等を添加してなる感熱性ま
たは感圧性接着剤をロールコーター等によつて支
持体1の裏面に膜厚5〜30ミクロンとなるように
塗布すればよい。
接着剤層5が感圧性接着剤層である本発明の磁
気貼合型記録体は、感圧性接着剤層を剥離紙で被
覆するか、或は保護塗膜層4に予め剥離処理を施
しておいて従来の粘着テープ同様ロール状に巻回
して使用に供すればよい。
本発明の磁気貼合型記録体に於いては、上記の
如く、透明または着色された保護塗膜層はSn蒸
着膜層を介して磁気塗膜層上に設けられているか
ら、層厚は薄くとも磁気塗膜層の色に左右されな
い任意の着色が可能であり、従つて、磁性体色と
は異なる種々の色彩が賦与されるとともにスペー
シングロスが極めて小さく入出力特性に優れた磁
気記録層を形成することができ、預金通帳、クレ
ジツトカード、コンピユーターの入出力媒体等に
有利に利用することができる。
次に、実施例によつて本発明を具体的に説明す
るが、実施例中の「部」は総て「重量部」を意味
する。
実施例 1
〔磁気塗料―()〕
(部)
1 γ―Fe2O3 30.0
2 レシチン 0.3
3 エポキシ樹脂(「エピコート834」、シエル
化学社製) 3.0
4 塩ビ―酢ビ共重合体(「ビニライト
VAGH」、ユニオンカーバイト社製) 15.0
5 低分子量ポリエチレン 0.3
6 トルエン 45.7
7 メチルエチルケトン 45.7
〔アンカー剤―()〕
(部)
1 ポリビニルブチラール(「エスレツク
BMS」、積水化学社製) 10
2 リン酸 1
3 無水クロム酸 0.5
4 イソプロピルアルコール 78
5 メチルエチルケトン 10
6 水 0.5
〔インキ―()〕
(部)
1 シアニン顔料 9
2 1/4ニトロセルロース 4
3 ポリアミド樹脂(「バーサミド940」、第1
ゼネラル社製) 15
4 低分子量ポリエチレン 1
5 アセチルトリブチルサイトレート 1
6 トルエン 40
7 イソプロピルアルコール 20
8 酢エチ 10
〔感熱性接着剤―()」
(部)
1 塩ビ―プロピオン酸ビニル共重合体(「電
化ビニル330WD」、電気化学社製) 20
2 アクリロニトリル―ブタジエンラバー
(「ハイカー1432」、日本ゼオン社製) 20
3 メチルエチルケトン 30
4 トルエン 30
厚さ38ミクロンのポリエステルフイルムを支持
体1とし、この表面に磁気塗料―()を膜厚14
ミクロンとなるように塗布して磁気塗膜層2を形
成し、この上にアンカー剤―()を膜厚0.2ミ
クロンとなるように塗布してアンカー剤層6を形
成した。次いで、この上にSnを膜厚500Åとなる
ように蒸着させてSn蒸着膜層3を形成した。更
に、この上にアンカー剤―()を膜厚0.2ミク
ロンとなるように塗布してアンカー剤層7を形成
した後、この上にインキ―()を膜厚1.5ミク
ロンとなるように塗布して保護塗膜層4を形成し
た。一方、上記支持体1の裏面には感熱性接着剤
―()を膜厚7ミクロンとなるように塗布して
感熱性接着剤層5を形成し、斯くして磁気貼合型
シートを作製した。
この磁気貼合型シートを幅20mm、長さ50mmに裁
断したものを銀行通帳用紙に重ね合わせ、これら
を120℃―600Kg/mの熱圧ロールの間を6m/分
の速度で通して熱圧着させ、斯くして鮮明なブル
ー色をした磁気記録層を有する磁気記録カードを
作製した。
この磁気記録カードの磁気特性、再生出力特
性、減磁率を表1に示す。
The present invention relates to a magnetically laminated recording medium, and in particular to a magnetically laminated type recording medium that is capable of forming a magnetic recording layer that is provided with various colors different from the color of the magnetic material and has extremely small spacing loss and excellent input/output characteristics. Regarding the body. It is possible to form a magnetic recording layer on bankbooks, credit cards, computer input/output media, etc. using a magnetic bonding type recording material with a magnetic coating layer on the surface of the support and an adhesive layer on the back side. Recently, this practice has become widespread, but along with this, there has been a gradual increase in the desire to give the magnetic recording layer a color different from the black to brown colors characteristic of magnetic materials due to aesthetic needs. There is. Recently, in response to this, magnetic bonding type recording media used in bank passbooks and the like have been provided in which a colored coating layer is provided directly on the magnetic coating layer. In a laminated recording medium, the color of the laminated magnetic recording layer must be quite dirty due to the lack of hiding power of the colored coating layer, and the color of the laminated magnetic recording layer must be quite dirty. If the thickness of the coating is increased in order to increase the magnetic field, the input/output characteristics of the magnetic recording layer will deteriorate, resulting in a disadvantage that detection errors are likely to occur. The present invention has been made in view of these points,
Therefore, the object of the present invention is to provide a material with various colors different from those of the magnetic material, whose color does not change at all over a long period of time, and which is aesthetically excellent, and which has extremely small spacing loss and excellent input/output characteristics. An object of the present invention is to provide a magnetic bonding type recording material in which a magnetic recording layer can be formed. As a result of intensive research, the present inventors basically established a Sn vapor deposition layer on the magnetic coating layer, and then added Sn on top of this.
It has been found that the above object can be achieved by providing a colored protective coating layer that protects the deposited film layer. That is, although the Sn vapor-deposited coating layer is extremely thin, it has extremely high hiding power, so it is possible to completely hide the color of the magnetic coating layer, and therefore, When a colored protective coating layer is provided on top of this, the coloring is effective even if the coating thickness is made considerably thinner. Therefore, a magnetically laminated recording body having such a basic configuration can form a magnetic recording layer that is imparted with a desired color, has extremely small spacing loss, and has excellent input/output characteristics. In addition, a magnetic bonding type recording medium with a transparent protective coating layer instead of the colored protective coating layer described above allows the metallic color of the metal vaporized layer to appear as is, and has excellent input/output characteristics. It has also been found that interesting magnetic recording layers can be formed. The present invention has been completed based on such knowledge, and according to the present invention, a magnetic coating layer 2, a Sn vapor deposition layer 3 and a protective coating are provided on the surface of a seal-shaped or film-shaped support 1. A magnetic bonding type recording body is provided in which the layers 4 are sequentially laminated and an adhesive layer 5 is provided on the back surface of the support 1. As the support 1, a plastic sheet or film is used, and sheets or films of polyester, polycarbonate, etc. are particularly suitable. There is no particular limit to the thickness of the support 1, but it is usually
Those with a diameter of about 20 to 100 microns are generally used. A magnetic coating layer 2 is provided on the surface of the support 1, and in order to form the magnetic coating layer 2, magnetic fine particles such as γ-iron oxide, Co-doped iron oxide, chromium dioxide, ferrite, etc. are contained. The magnetic paint may be applied to the surface of the support 1 using a roll coater or the like. Further, the film thickness may be appropriately determined in consideration of storage capacity and the like, and is usually 5 to 20 microns. There are no particular restrictions on the magnetic paint; for example, the binder component may be cellulose resin, vinyl chloride resin, vinyl chloride-vinyl acetate copolymer, urethane resin, epoxy resin, polyester resin, styrene-butadiene rubber, etc., and it is preferable to use a binder component suitable for these resins. It is sufficient to use a magnetic coating material to which a curing agent and various auxiliary agents are added as necessary. A Sn evaporated film layer 3 is provided on the magnetic coating layer 2, but if we consider it only from the viewpoint of hiding the color of the magnetic coating layer without disturbing the magnetic properties of the magnetic coating layer 2, the Sn evaporation film is Mg.Al.Zn.Pt.Au.Ag instead of layer 3
It is also possible to use a vapor-deposited film layer according to et al. However, if the vapor-deposited film layer made of these metals is in contact with the magnetic coating layer, during long-term storage, the metals in the metal-deposited film layer and the γ-iron oxide and ferrite contained in the magnetic coating layer will be absorbed. Finger fat, etc. between magnetic particles such as
An electrochemical reaction occurs, which is thought to be caused by moisture, and as a result unsightly black spots often appear on the metallized film layer. However, when Sn is used as the vapor-deposited metal, no such spots are observed. A known metal vapor deposition machine may be used to form the Sn vapor deposition film layer 3. Further, the film thickness may be a minimum thickness sufficient to completely hide the magnetic coating layer 2, and may be, for example, 100 to 1000 A°. If the interlayer adhesion between the magnetic coating layer 2 and the Sn vapor deposition layer 3 is insufficient, in order to reinforce this, the magnetic coating layer 2 and the Sn vapor deposition layer 3 may be bonded together as necessary.
What is necessary is just to interpose the anchor agent layer 6 between them. As the anchor agent, commercially available anchor agents such as vinyl chloride-vinyl acetate copolymer, epoxy resin, and polyamide resin, and polyvinyl butyral-dichromate-carryphosphate wash primers can be used. In order to form the anchor agent layer 6, the above-mentioned anchor agent is coated on the magnetic coating layer 2 with a roll coater to form a film thickness.
The coating should be applied to a thickness of 0.01 to 1.0 microns. A protective coating layer 4 is provided on the Sn vapor deposition film layer 3, and the protective coating layer 4 protects the Sn vapor deposition film layer 3.
This is for coloring if necessary,
It does not matter whether it is transparent or opaque, colored or uncolored. That is, the protective coating layer 4 may be a single layer of either a transparent layer or a colored layer, or may be a composite layer thereof. To form the protective coating layer 4, the Sn vapor-deposited layer 3 is coated or printed with transparent or colored paint or ink using a roll coater, gravure printer, or the like. Examples of such transparent or colored paints or inks include cellulose acetate butyrate, cellulose resins such as nitrocellulose, acrylic resins, butyral resins, vinyl chloride-vinyl acetate copolymers, polyester resins, alkyd resins, and urethane resins. Thermoplastic or Thermosetting paints or inks can be used. The thickness of the protective coating layer 4 is preferably as thin as possible from the viewpoint of input/output characteristics, but in consideration of balance with strength, durability, etc., it is preferably in the range of 0.1 to 5 microns. If the interlayer adhesion between the Sn vapor deposited film layer 3 and the protective coating layer 4 is insufficient, in order to reinforce this, the Sn vapor deposited film layer 3 and the protective coating film layer 4 may be
The anchor agent layer 7 may be interposed between the two, and the same anchor agent as described above may be used as the anchor agent. On the other hand, an adhesive layer 5 is provided on the back surface of the support 1, and the adhesive layer 5 may be either a heat-sensitive adhesive layer or a pressure-sensitive adhesive layer. To form the adhesive layer 5, for example, vinyl chloride resin, vinyl acetate resin, vinyl chloride-vinyl acetate copolymer, urethane resin, acrylonitrile butadiene resin, polyester resin, cellulose resin, vinyl chloride-vinylidene chloride copolymer, epoxy resin can be used. A heat-sensitive or pressure-sensitive adhesive made of natural rubber, rosin, etc. with addition of plasticizers, auxiliary agents, etc. as necessary is coated on the back surface of the support 1 with a roll coater or the like to a film thickness of 5 to 30 microns. Just apply it like this. In the magnetically bonded recording material of the present invention in which the adhesive layer 5 is a pressure-sensitive adhesive layer, the pressure-sensitive adhesive layer is covered with a release paper, or the protective coating layer 4 is subjected to a release treatment in advance. Then, it can be used by winding it into a roll like a conventional adhesive tape. In the magnetically laminated recording material of the present invention, as described above, the transparent or colored protective coating layer is provided on the magnetic coating layer via the Sn vapor deposition layer, so the layer thickness is It is possible to apply any coloring that is not affected by the color of the magnetic coating layer, even if it is thin.Therefore, magnetic recording can be provided with various colors different from those of magnetic materials, and has extremely low spacing loss and excellent input/output characteristics. It can be used advantageously for bankbooks, credit cards, computer input/output media, etc. Next, the present invention will be specifically explained with reference to Examples, in which all "parts" mean "parts by weight". Example 1 [Magnetic paint - ()] (parts) 1 γ-Fe 2 O 3 30.0 2 Lecithin 0.3 3 Epoxy resin ("Epicote 834", manufactured by Ciel Chemical Co., Ltd.) 3.0 4 PVC-vinyl acetate copolymer ("Vinyrite")
VAGH, manufactured by Union Carbide) 15.0 5 Low molecular weight polyethylene 0.3 6 Toluene 45.7 7 Methyl ethyl ketone 45.7 [Anchor agent - ()] (parts) 1 Polyvinyl butyral (Eslec
10 2 Phosphoric acid 1 3 Chromic anhydride 0.5 4 Isopropyl alcohol 78 5 Methyl ethyl ketone 10 6 Water 0.5 [Ink ()] (Parts) 1 Cyanine pigment 9 2 1/4 Nitrocellulose 4 3 Polyamide Resin (“Versamide 940”, 1st
General) 15 4 Low molecular weight polyethylene 1 5 Acetyl tributyl citrate 1 6 Toluene 40 7 Isopropyl alcohol 20 8 Ethyl acetate 10 [Heat-sensitive adhesive - ()' (parts) 1 Vinyl chloride - vinyl propionate copolymer (' 20 2 Acrylonitrile-butadiene rubber (``Hiker 1432'', manufactured by Nippon Zeon Co., Ltd.) 20 3 Methyl ethyl ketone 30 4 Toluene 30 A polyester film with a thickness of 38 microns is used as support 1, and the surface is Magnetic paint - () film thickness 14
A magnetic coating layer 2 was formed by applying the magnetic coating layer 2 to a thickness of 0.2 microns, and an anchoring agent layer 6 was formed by applying an anchor agent (2) to a thickness of 0.2 microns thereon. Next, Sn was vapor-deposited thereon to a thickness of 500 Å to form a Sn vapor-deposited film layer 3. Further, an anchor agent layer 7 was formed by applying an anchor agent () to a thickness of 0.2 microns, and then an ink layer () was applied to this layer to a thickness of 1.5 microns. A protective coating layer 4 was formed. On the other hand, a heat-sensitive adhesive layer 5 was formed by applying a heat-sensitive adhesive () to the back surface of the support 1 to a thickness of 7 microns, thus producing a magnetically laminated sheet. . This magnetic bonding type sheet is cut into 20mm wide and 50mm long sheets, stacked on bank passbook paper, and then passed through hot pressure rolls at 120℃ - 600Kg/m at a speed of 6m/min to bond under heat. In this way, a magnetic recording card having a magnetic recording layer with a clear blue color was produced. Table 1 shows the magnetic properties, reproduction output characteristics, and demagnetization rate of this magnetic recording card.
【表】
また、上記磁気貼合型シートおよび磁気記録カ
ードを6ケ月間室内に保存して、Sn蒸着膜層と
磁気塗膜層との局部的電気化学反応によつて外観
に斑点等の変化が生ずるか否か調べたが、変化は
全く認められなかつた。
比較例 1
厚さ38ミクロンのポリエステルフイルムを支持
体とし、この表面に磁気塗料―()を膜厚14ミ
クロンとなるように塗布して磁気塗膜厚を形成
し、次いで、この上にインキ―()を膜厚1.5
ミクロンとなるように塗布して保護塗膜層を形成
した。一方、上記支持体の裏面に感熱性接着剤層
―()を膜厚7ミクロンとなるように塗布して
感熱性接着剤層を形成し、斯くして従来型の磁気
貼合型シートを作製した。
また、保護塗膜層の厚さを、それぞれ
3.0.6.0.9.0ミクロンとする以外は上記と同様にし
て従来型の磁気貼合型シートを作製した。
これらの磁気貼合型シートを用い、実施例1と
同様にして、磁気記録カードを作製した。これら
の磁気記録カードの磁気特性、色および再生出力
特性を表2に示す。[Table] In addition, when the above-mentioned magnetically laminated sheets and magnetic recording cards were stored indoors for 6 months, changes in appearance such as spots were observed due to local electrochemical reactions between the Sn vapor-deposited film layer and the magnetic coating layer. We investigated whether or not this occurred, but no change was observed. Comparative Example 1 A polyester film with a thickness of 38 microns was used as a support, and magnetic paint () was applied to the surface of the support to a film thickness of 14 microns to form a magnetic coating film, and then ink was applied on top of this. () Film thickness 1.5
A protective coating layer was formed by applying the coating to a micron thickness. On the other hand, a heat-sensitive adhesive layer () was applied to the back side of the support to a thickness of 7 microns to form a heat-sensitive adhesive layer, thus producing a conventional magnetically laminated sheet. did. In addition, the thickness of the protective coating layer is
A conventional magnetic bonding type sheet was produced in the same manner as above except that the thickness was 3.0.6.0.9.0 microns. A magnetic recording card was produced in the same manner as in Example 1 using these magnetically bonded sheets. Table 2 shows the magnetic properties, colors, and reproduction output characteristics of these magnetic recording cards.
【表】
比較例 2
実施例1に於いて、蒸着金属Snの替りにAl.
Ag.Znを使用する以外は同実施例と同様にして鮮
明なブルー色を有する磁気貼合型シートおよび磁
気記録カードを作製した。これらの磁気記録カー
ドの磁気特性、再生出力特性を表3に示す。ま
た、これらの磁気貼合型シートをおよび磁気記録
カードを室内で6ケ月間保存して外観の変化を観
察した。その結果を表4に示す。[Table] Comparative Example 2 In Example 1, Al.
A magnetic bonding type sheet and a magnetic recording card having a clear blue color were produced in the same manner as in the same Example except that Ag.Zn was used. Table 3 shows the magnetic properties and reproduction output characteristics of these magnetic recording cards. In addition, these magnetically bonded sheets and magnetic recording cards were stored indoors for 6 months and changes in appearance were observed. The results are shown in Table 4.
【表】【table】
部
1 自己硬化型シリコン樹脂(東芝シリコン
「YSR―3022」、東芝シリコン社製) 19
2 硬化促進剤(東芝シリコン「YC―6831」、
同社製) 0.5
3 硬化促進剤(東芝シリコン「XC―6953」、
同社製) 0.5
4 ゴム揮 50
5 メチルエチルケトン 20
6 イソプロピルアルコール 10
〔感圧性接着剤―()〕
部
1 アクリル樹脂(「KP―351」、日本カーバイ
ト社製) 50
2 メチルエチルケトン 25
3 トルエン 25
厚さ38ミクロンのポリエステルフイルムを支持
体1とし、この表面に磁気塗料―()を膜厚14
ミクロンとなるように塗布して磁気塗膜層2を形
成し、この上にSnを膜厚500Åとなるように蒸着
させて金属蒸着膜層3を形成した。次いで、この
上にアンカー剤―()を膜厚0.2ミクロンとな
るように塗布してアンカー剤層7を形成した後、
インキ―()を膜厚1.5ミクロンとなるように
塗布し、更に透明塗料―()を膜厚0.2ミクロ
ンとなるように塗布して着色層と透明層が複合し
た保護塗膜層4を形成した。一方、上記支持体1
の裏面には感圧性接着剤―()を膜厚7ミクロ
ンとなるように塗布して接着剤層5を形成し、斯
くして作製した磁気貼合型シートをロール状に巻
回した後、これをテープ状に切断した。
斯くして作製された磁気貼合型テープを磁気元
帳用紙に貼り合わせ、次いで、これらを圧力40
Kg/mの加圧ロールの間を5m/分の速度で通し
て圧着させて磁気元帳を作製した。
この磁気元帳の磁気特性、再生出力特性、減磁
率を表5に示す。
Part 1 Self-curing silicone resin (Toshiba Silicon "YSR-3022", manufactured by Toshiba Silicon Co., Ltd.) 19 2 Curing accelerator (Toshiba Silicon "YC-6831",
(manufactured by the same company) 0.5 3 Curing accelerator (Toshiba Silicon "XC-6953",
(manufactured by the same company) 0.5 4 Rubber 50 5 Methyl ethyl ketone 20 6 Isopropyl alcohol 10 [Pressure sensitive adhesive - ()] Part 1 Acrylic resin (“KP-351”, manufactured by Nippon Carbide Co., Ltd.) 50 2 Methyl ethyl ketone 25 3 Toluene 25 Thickness A 38 micron polyester film is used as the support 1, and magnetic paint () is applied to the surface with a thickness of 14
A magnetic coating layer 2 was formed by applying the magnetic coating to a thickness of microns, and a metal vapor deposition layer 3 was formed by vapor-depositing Sn to a thickness of 500 Å on top of the magnetic coating layer 2. Next, an anchor agent layer 7 was formed by applying an anchor agent () to a film thickness of 0.2 microns, and then
Ink () was applied to a film thickness of 1.5 microns, and transparent paint () was further applied to a film thickness of 0.2 microns to form a protective coating layer 4 consisting of a colored layer and a transparent layer. . On the other hand, the support 1
A pressure-sensitive adhesive () was applied to the back side of the sheet to a thickness of 7 microns to form an adhesive layer 5, and the magnetically laminated sheet thus prepared was wound into a roll. This was cut into tape shapes. The magnetically bonded tape thus produced was bonded to magnetic ledger paper, and then they were applied under a pressure of 40°C.
A magnetic ledger was produced by passing it between pressure rolls of Kg/m at a speed of 5 m/min and pressing it. Table 5 shows the magnetic properties, reproduction output characteristics, and demagnetization rate of this magnetic ledger.
第1〜3図は本発明の磁気貼合型記録体の実施
例を示す部分断面図である。
1 to 3 are partial cross-sectional views showing examples of the magnetic bonding type recording material of the present invention.
Claims (1)
に磁気塗膜層2、Sn蒸着膜層3および保護塗膜
層4を順次積層状に設けるとともに支持体1の裏
面に接着剤層5が設けられた磁気貼合型記録体。 2 接着剤層5が感熱性接着剤層である特許請求
の範囲第1項記載の磁気貼合型記録体。 3 接着剤層5が感圧性接着剤層である特許請求
の範囲第1項記載の磁気貼合型記録体。 4 保護塗膜層4が透明塗膜層、着色塗膜層また
はそれらの複合塗膜層である特許請求の範囲第2
項または第3項記載の磁気貼合型記録体。[Claims] 1. A magnetic coating layer 2, a Sn vapor deposition layer 3, and a protective coating layer 4 are sequentially laminated on the surface of a sheet-like or film-like support 1, and are adhered to the back surface of the support 1. A magnetic bonding type recording body provided with an agent layer 5. 2. The magnetically bonded recording material according to claim 1, wherein the adhesive layer 5 is a heat-sensitive adhesive layer. 3. The magnetically bonded recording material according to claim 1, wherein the adhesive layer 5 is a pressure-sensitive adhesive layer. 4. Claim 2, in which the protective coating layer 4 is a transparent coating layer, a colored coating layer, or a composite coating layer thereof.
The magnetic bonding type recording material according to item 1 or 3.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3283877A JPS53118104A (en) | 1977-03-25 | 1977-03-25 | Magnetic combination type recording material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3283877A JPS53118104A (en) | 1977-03-25 | 1977-03-25 | Magnetic combination type recording material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS53118104A JPS53118104A (en) | 1978-10-16 |
JPS6315657B2 true JPS6315657B2 (en) | 1988-04-05 |
Family
ID=12369954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3283877A Granted JPS53118104A (en) | 1977-03-25 | 1977-03-25 | Magnetic combination type recording material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS53118104A (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5756331Y2 (en) * | 1978-07-07 | 1982-12-04 | ||
JPS5756330Y2 (en) * | 1978-07-07 | 1982-12-04 | ||
JPS55149837U (en) * | 1979-04-12 | 1980-10-28 | ||
JPS5654634A (en) * | 1979-10-08 | 1981-05-14 | Tokyo Jiki Insatsu Kk | Colored magnetic recording medium |
JPS56104057A (en) * | 1980-01-24 | 1981-08-19 | Hitachi Maxell | Adhesive colored magnetic sheet |
JPS56143540A (en) * | 1980-04-10 | 1981-11-09 | Fuji Photo Film Co Ltd | Magnetic recording medium |
JPS6220899Y2 (en) * | 1980-12-04 | 1987-05-27 | ||
JPS5839739U (en) * | 1981-09-04 | 1983-03-15 | 共同印刷株式会社 | colored magnetic recording media |
JPS5865643U (en) * | 1981-10-24 | 1983-05-04 | 共同印刷株式会社 | colored magnetic recording media |
JPS5865642U (en) * | 1981-10-24 | 1983-05-04 | 共同印刷株式会社 | colored magnetic recording media |
JPS58105428A (en) * | 1981-12-17 | 1983-06-23 | Kyodo Printing Co Ltd | Colored magnetic recording medium |
JPH0630960B2 (en) * | 1983-04-27 | 1994-04-27 | 大日本印刷株式会社 | Thermal magnetic recording medium |
JPS6018388A (en) * | 1983-07-11 | 1985-01-30 | Dainippon Printing Co Ltd | Thermal magnetic recording medium |
JPH0780373B2 (en) * | 1987-05-01 | 1995-08-30 | 日本加工製紙株式会社 | Magnetic recording paper |
JPH023875U (en) * | 1988-12-13 | 1990-01-11 | ||
JPH04191097A (en) * | 1990-11-27 | 1992-07-09 | Sumitomo Bakelite Co Ltd | Magnetic card |
JP2650653B2 (en) * | 1993-12-10 | 1997-09-03 | 大日本印刷株式会社 | Thermal magnetic recording media |
JP2007188602A (en) * | 2006-01-13 | 2007-07-26 | Dainippon Printing Co Ltd | Recording medium and reading and writing device |
USD854083S1 (en) | 2013-03-27 | 2019-07-16 | Jpmorgan Chase Bank, N.A. | Hybrid transaction device |
JP6126512B2 (en) | 2013-10-15 | 2017-05-10 | 株式会社神戸製鋼所 | Compressor |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5633448U (en) * | 1979-08-21 | 1981-04-01 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5314242Y2 (en) * | 1973-01-29 | 1978-04-15 | ||
JPS537690Y2 (en) * | 1974-10-18 | 1978-02-27 |
-
1977
- 1977-03-25 JP JP3283877A patent/JPS53118104A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5633448U (en) * | 1979-08-21 | 1981-04-01 |
Also Published As
Publication number | Publication date |
---|---|
JPS53118104A (en) | 1978-10-16 |
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