JPH0158078B2 - - Google Patents
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- Publication number
- JPH0158078B2 JPH0158078B2 JP56200394A JP20039481A JPH0158078B2 JP H0158078 B2 JPH0158078 B2 JP H0158078B2 JP 56200394 A JP56200394 A JP 56200394A JP 20039481 A JP20039481 A JP 20039481A JP H0158078 B2 JPH0158078 B2 JP H0158078B2
- Authority
- JP
- Japan
- Prior art keywords
- ink layer
- heat
- recording medium
- thermal
- paper
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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- 239000000463 material Substances 0.000 claims description 22
- 238000010438 heat treatment Methods 0.000 claims description 19
- 238000012546 transfer Methods 0.000 claims description 16
- 239000000314 lubricant Substances 0.000 claims description 15
- 238000002844 melting Methods 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 229920002545 silicone oil Polymers 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 3
- 230000000149 penetrating effect Effects 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- 239000012943 hotmelt Substances 0.000 description 9
- 238000007639 printing Methods 0.000 description 9
- 239000003086 colorant Substances 0.000 description 8
- 239000010439 graphite Substances 0.000 description 7
- 229910002804 graphite Inorganic materials 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000010408 film Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- -1 polychlorotrifluoroethylene Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 4
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 238000001454 recorded image Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- JPIYZTWMUGTEHX-UHFFFAOYSA-N auramine O free base Chemical compound C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 JPIYZTWMUGTEHX-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- CCDWGDHTPAJHOA-UHFFFAOYSA-N benzylsilicon Chemical compound [Si]CC1=CC=CC=C1 CCDWGDHTPAJHOA-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- CMXPERZAMAQXSF-UHFFFAOYSA-M sodium;1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate;1,8-dihydroxyanthracene-9,10-dione Chemical compound [Na+].O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O.CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC CMXPERZAMAQXSF-UHFFFAOYSA-M 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000010689 synthetic lubricating oil Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/392—Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Impression-Transfer Materials And Handling Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Description
本発明はサーマルフアクシミリなどの熱記録装
置に好適に使用されうる新規な熱記録媒体に関す
る。
近時、フアクシミリ通信の発達がめざましい
が、フアクシミリ装置に用いられる記録方法の中
で感熱記録法はその代表的なものである。
第3図は感熱紙を用いるフアクシミリ装置、い
わゆるサーマルフアツクスの一例を示す概略説明
図である。
すなわち感熱紙1をピンチローラ2で加熱ヘツ
ド3に押付け、感熱紙1を加熱発色させながらピ
ンチローラ2で感熱紙1をあるピツチごとに送り
出し、ついでえられた画像をカツター4で切り取
るようになつているものである。
かかる従来公知の感熱記録方式は現像や定着が
不要で、信頼性および保守性にすぐれているなど
の利点を有する反面、感熱紙を用いるために生ず
る記録の改ざん性や保守性に問題点を有してい
る。そのため薄いフイルム上に熱溶融性インキ層
を塗布し、該インキ層の面に普通紙を重ね合わせ
て前記フイルムの上から加熱ヘツドで加熱し、前
記インキ層を溶融させて普通紙に転移させる熱転
写記録法が提案されている。該記録法は従来の感
熱紙記録方法の有する利点を損なうことなく、普
通紙に記録しうるという特徴を有する。
かかる熱転写記録方法においては、従来より基
材であるフイルムとしてポリエステルフイルムが
使用されている。しかしながら、前述のごときフ
アクシミリ装置に厚さが10μ程度と薄いポリエス
テルフイルムを用いたばあい、鮮明で解像度の高
い記録を行ないうるが、フイルムの収縮によりシ
ワが生じて記録ムラや記録不能になるという欠点
がある。また厚さが25μ程度と厚いフイルムを用
いたばあい、シワの発生は防止しうる反面、充分
な濃度の記録をうるためには加熱温度を上げる必
要があり、そのためフイルムが溶融して加熱ヘツ
ドに付着するという欠点を有する。
一方、ポリエステルフイルムなどのプラスチツ
クフイルムに代えて薄葉紙などの紙を用いること
が提案されている。薄葉紙はそれ自体耐熱性にす
ぐれ、加熱ヘツドとの接触により収縮してシワを
生じたり、加熱ヘツドに付着したりすることがな
いという利点を有する反面、表面の平滑性に劣る
ために、熱溶融性インキ層の溶融転写性(剥離
性)がわるくなり、印字像の鮮明さに劣り、かつ
ムラや欠けが生じやすいという欠点がある。さら
に薄葉紙上に熱溶融性インキ層を塗布するため
に、該インキ層が薄葉紙の内部に浸透し、ついに
は裏面にまで達して加熱ヘツドを汚染するという
欠点がある。
本発明は叙上の欠点を排除すべく完成されたも
のであつて、基材上に設けられた熱溶融性インキ
層を基材の背面から加熱ヘツドで加熱し、該イン
キ層の加熱された部位を選択的に受容体に転写し
て印像を形成する記録方式に用いる熱転写記録媒
体において、前記基材が薄葉紙であり、かつ前記
熱溶融性インキ層に薄葉紙内へのインキの浸透を
防止し、該インキ層の剥離性を向上せしめうる潤
滑性剤が含有されてなる熱転写記録媒体を要旨と
するものである。
本発明における前記薄葉紙は坪量が10〜30g/
m2の薄い紙であつて、例えばワンタイムカーボン
原紙、ロウ紙用原紙、コピー紙、タイプライター
原紙などがあげられる。
本発明の熱転写記録媒体は、基材として薄葉紙
を用いるうえで熱溶融性インキ層に基材への浸透
防止効果と印字時における基材からの剥離効果と
を具備せしめるべく、熱溶融性インキ層に潤滑性
剤を含有せしめるときは、該インキ層の溶融時に
おける粘度が向上し、基材内への浸透が防止され
ると共に、その潤滑性によりインキ層の剥離(溶
融転写)が速やかに行なわれ、かつ少ない熱エネ
ルギーで鮮明で欠けやムラのない印字像を形成せ
しめうるというまつたく新たな知見に基づいて完
成されたものである。
しかして本発明における潤滑性剤としては、た
とえばシリコーンオイル、ポリアルキレングリコ
ール、フツ素油、ポリα−オレフインなどの合成
潤滑油や二硫化モリブデン、黒鉛などの固体潤滑
剤などがあげられる。
前記シリコーンオイルとしては、たとえばジメ
チルシリコーンオイル(たとえば信越化学工業(株)
製のKF−96)、フエニルメチルシリコーンオイル
(たとえばダウコーニング社製のモリコート33)
などがあげられる。前記ポリアルキレングリコー
ルとしては、たとえばポリオキシプロピレングリ
コールモノエーテル(たとえば三洋化成工業(株)製
のニユーポールLB625)、ポリオキシアルキレン
誘導体(たとえば日本油脂(株)製のユニルーブ
MB38)などがあげられる。前記フツ素油として
は、たとえばポリクロロトリフルオロエチレン
(たとえばダイキン工業(株)製のダイフロイル10)
などがあげられる。前記ポリα−オレフインとし
ては、たとえばα−オレフインオリゴマー(たと
えばライオン油脂(株)製のリポルーブ#4)などが
あげられる。また前記二硫化モリブデンとして
は、たとえば鉱油ペースト状ないし合成油ベース
のもの(たとえばダウコーニング社製のモリコー
トG、住鉱潤滑剤(株)のモリペーストHなど)があ
げられる。さらに前記黒鉛としては、たとえば合
成油ペースト状の黒鉛(たとえば日本黒鉛工業(株)
製のピアシングオイル#5)や日立粉末治金(株)の
黒鉛オイル(ヒタゾルGO−102)などがあげら
れる。かかる潤滑性剤は熱溶融性インキ層総量に
対して0.1〜15部(重量部、以下同様)、より好ま
しくは0.5〜5部であるのが好ましい。潤滑性剤
の使用量が前記範囲より小なるときは浸透防止や
剥離性向上の効果がなく、また前記範囲より大な
るときは塗布されたインキ層が剥離することとな
り、いずれも好ましくない。かかる潤滑性剤は熱
溶融性インキ層に均一に分散した状態で基材上に
塗布される。熱溶融性インキ層を形成する他の配
合成分は通常の熱溶融性インキ層における配合成
分をそのまま使用することができ、とくにその使
用が制限されるものではない。熱溶融性インキ層
を形成する他の配合成分としては、たとえば着色
剤、バインダー剤、石油樹脂、柔軟剤などがあげ
られる。
しかして熱溶融性インキ層は前記潤滑性剤、着
色剤、バインダー剤、石油樹脂および柔軟剤から
なる組成物をホツトメルコーテイングするか、ま
たは該組成物を適宜の溶媒に分散せしめてなる塗
布液をソルベンコーテイングして形成される。バ
インダ剤としては、たとえばカルナバワツクス、
オーリキユリーワツクス、マイクロクリスタリン
ワツクスなどのワツクス類、あるいは低分子量ポ
リエチレン、ポリステアリン酸ビニルなどの樹脂
類のごとき容易に熱溶融しうる物質が好適に使用
される。また柔軟剤としては、たとえばポリ酢酸
ビニル、ポリスチレン、スチレン−ブタジエン共
重合体、セルロースエステル類、セルロースエー
テル類、アクリル系樹脂類などのごとき容易に熱
溶融しうる物質が好適に使用される。着色剤とし
ては従来より複写紙の分野で多用されている各種
染料または顔料が特別の制限なしに使用可能であ
る。
これらバインダー剤、石油樹脂、柔軟剤および
着色剤は、熱溶融性インキ層総量100部(重量部、
以下同様)に対して、それぞれ5〜55部、0.5〜
10部、5〜40部および2〜25部の配合割合とする
のが好ましく、そのばあいには形成される熱溶融
性インキ層の溶融転写性がすこぶる良好である。
なお本発明においては、前記着色剤として感熱
発色剤を用いてもよい。該感熱発色剤は酸と反応
して発色しうる染料前駆体と常温で固体ないし半
固体の有機または無機酸とからなるものであり、
かかる感熱発色剤バインダー剤などによつて均一
に分散または溶解させて実質的に無色または淡色
の熱溶融性インキ層が形成される。かかる感熱発
色剤を用いてえられる熱溶融性インキ層は加熱ヘ
ツドから発生する熱によつて、分散状の前記固体
ないし半固体の酸が溶融液化し、前記染料前駆体
と発色反応して鮮明な記録像を形成する。
染料前駆体としては、フエノチアジン系、フル
オラン系、オーラミン系、トリフエニルメタン
系、スピロピラン系などの各種染料前駆体がいず
れも好適に用いられる。
また前記有機または無機酸としては、たとえば
安息香酸、酒石酸、クエン酸、サリチル酸、ステ
アリン酸、没食子酸、ビスフエノールA、ナフト
エ酸、ピロリン酸、メタリン酸などが好適に用い
られる。
本発明における熱溶融性インキ層は厚さが15μ
以下、好ましくは2〜5μの範囲で好適に用いら
れる。厚さが前記範囲より大なるばあいはインキ
層の転写に多量の熱エネルギーを必要とし、また
解像度が低下するために好ましくない。
つぎに本発明の熱転写記録媒体を用いて第3図
で示したフアクシミリ装置により記録するばあい
について説明する。
すなわち第1図および第2図は本発明の熱記録
媒体の記録方式を示す概略説明図である。
第1図および第2図において、5は基材7と熱
溶融性インキ層8からなる本発明の熱記録媒体、
6はコピーシート、2々よび3はそれぞれ前述の
ピンチローラおよび印字パターンの構成により、
1×7、5×7、7×9などのドツト素子マトリ
ツクス状に発熱抵抗素子が配列されている加熱ヘ
ツド、9および10は加熱ヘツド3にパルスを印
加するための端子、11はコピーシート上に形成
された記録像である。
第1図において熱記録媒体5は、その熱溶融性
インキ層8がコピーシート6と対向するごとく重
ね合されて装着されており、熱記録媒体5の基材
7は加熱ヘツド3と接して、一方コピーシート6
はピンチローラ2と接している。なおコピーシー
ト6は通常の紙である。端子9および10から印
字パターンに対応したパルスが印加されると、加
熱ヘツド3は印字パターンに応じたドツトがジユ
ール熱を発生する。該ジユール熱は基材7を経て
熱溶融性インキ層8まで瞬間的に伝達し、該イン
キ層8を印字パターンに応じて部分的に溶融す
る。
第2図に示されるごとくパルス印加がおわる
と、加熱ヘツド3、熱記録媒体5およびコピーシ
ート6は互いに分離した状態となり、そのときに
印字パターンに応じて溶融された熱溶融インキ層
の部分が基材7から剥離してコピーシート6の上
面に転写され、印字パターンどおりの印字像11
を形成する。
このようにしてパルス印加が繰返され、記録が
連続的に行なわれる。
なお本発明においては前記基材7の熱溶融性イ
ンキ層8を設けていない他面に従来公知の感熱発
色層を設けて記録およびコピーシート6への複写
をも同時に行ないうるようにしてもよく、さらに
本発明の熱記録媒体5と加熱ヘツド3との間に他
の感熱紙を介在せしめるようにしてもよい。
かくして形成される印字像11は、基材7であ
る薄葉紙が耐熱性および熱伝導性にすぐれてお
り、かつ熱溶融性インキ層8が基材7からの剥離
性にすぐれているために、鮮明で解像度が高く、
ムラや抜けがないというすぐれた利点を有し、さ
らに少ない熱エネルギーで前記インキ層8を速や
かに溶融転写せしめうるために印字スピードの向
上をもはかることができるという利点を有する。
しかも前記熱溶融性インキ層8は潤滑性剤を含有
することにより、基材7である薄葉紙内に浸透す
ることがなく、それゆえ本発明の記録媒体は加熱
ヘツド3の汚染といつたおそれがなく、サーマル
フアクシミリやサーマルプリンター用の記録媒体
として好適に採用しうるものである。
つぎに実施例および比較例をあげて本発明の記
録媒体を説明する。
実施例 1
下記組成を有する熱溶融性インキ組成物100部
に対して潤滑性剤としてジメチルシリコーンオイ
ル(信越化学工業(株)製のKF−96)の0.6部を加
え、均一に混合したのち、基材(ワンタイムカー
ボン原紙)上に塗布し、厚さ4.5μの熱溶融性イン
キ層をえた。
(成分) (部)
カルナバワツクス 45
石油樹脂 3
エチルセルロース 30
カーボンブラツク 22
実施例 2
ジメチルシリコーンオイルの添加量を4.5部と
したほかは実施例1と同様にして熱溶融性インキ
層をえた。
比較例 1
ジメチルシリコーンオイルを添加しなかつたほ
かは実施例1と同様にして熱溶融性インキ層をえ
た。
比較例 2
ジメチルシリコーンオイルの添加量を20部とし
たほかは実施例1と同様にして熱溶融性インキ層
をえた。
かくしてえられた各熱転写記録媒体について基
材裏面へのインキの浸透性およびインキ層の剥離
性を調べた。すなわちインキの浸透性はインキを
基材上に塗布したのち、室温下で1日放置し、基
材裏面に浸出したインキの有無を観察した。また
インキ層の剥離性はサーマルプリンター(沖電気
工業(株)製のサーマルプリンター100)によつて普
通紙上に30字/秒の速度で印字したときの印字部
位におけるインキの残留度合、すなわち完全に転
写せずに基材に付着した残留インキの有無を観察
した。これらの試験結果を次表に示す。
The present invention relates to a novel thermal recording medium that can be suitably used in thermal recording devices such as thermal facsimile machines. Recently, the development of facsimile communication has been remarkable, and thermal recording is a typical recording method used in facsimile devices. FIG. 3 is a schematic explanatory diagram showing an example of a facsimile device using thermal paper, a so-called thermal fax. In other words, the thermal paper 1 is pressed against the heating head 3 by the pinch roller 2, and while the thermal paper 1 is heated and colored, the pinch roller 2 feeds the thermal paper 1 at a certain pitch, and the resulting image is then cut out by the cutter 4. It is something that Such conventional heat-sensitive recording methods do not require development or fixing, and have the advantage of being excellent in reliability and maintainability. are doing. For this purpose, a heat-melting ink layer is coated on a thin film, plain paper is placed on the surface of the ink layer, and the film is heated from above with a heating head to melt the ink layer and transfer it to the plain paper.Thermal transfer A recording method is proposed. This recording method has the feature that recording can be performed on plain paper without sacrificing the advantages of conventional thermal paper recording methods. In such thermal transfer recording methods, polyester films have conventionally been used as the base film. However, if a thin polyester film with a thickness of about 10 μm is used in the facsimile device as described above, clear and high-resolution recording can be made, but wrinkles may occur due to shrinkage of the film, resulting in uneven recording or the inability to record. There are drawbacks. In addition, when using a thick film with a thickness of about 25 μm, wrinkles can be prevented, but in order to obtain a record of sufficient density, it is necessary to raise the heating temperature, which may cause the film to melt and cause the heating head to be heated. It has the disadvantage of adhering to. On the other hand, it has been proposed to use paper such as tissue paper instead of plastic film such as polyester film. Tissue paper itself has excellent heat resistance and has the advantage of not shrinking and wrinkled by contact with the heating head, nor sticking to the heating head. The disadvantages are that the melt transferability (releasability) of the ink layer deteriorates, the sharpness of the printed image is poor, and unevenness and chipping are likely to occur. Furthermore, since the hot-melt ink layer is applied onto the tissue paper, there is a disadvantage that the ink layer penetrates into the interior of the tissue paper, eventually reaching the back surface and contaminating the heating head. The present invention has been completed in order to eliminate the above-mentioned drawbacks, and the present invention has been completed by heating a hot-melt ink layer provided on a base material with a heating head from the back side of the base material. In a thermal transfer recording medium used in a recording method in which a portion is selectively transferred to a receptor to form a printed image, the base material is thin paper, and the heat-melting ink layer prevents ink from penetrating into the thin paper. The gist of the present invention is a thermal transfer recording medium containing a lubricant that can improve the releasability of the ink layer. The thin paper in the present invention has a basis weight of 10 to 30 g/
m 2 thin paper, such as one-time carbon base paper, wax paper base paper, copy paper, typewriter base paper, etc. The thermal transfer recording medium of the present invention uses thin paper as a base material, and the heat-fusible ink layer has an effect of preventing penetration into the base material and an effect of peeling from the base material during printing. When a lubricant is contained in the ink layer, the viscosity of the ink layer when melted increases, preventing penetration into the base material, and its lubricity allows the ink layer to be quickly peeled off (melt transfer). It was completed based on the new knowledge that it is possible to form a clear printed image without chipping or unevenness with less heat energy. Examples of the lubricating agent in the present invention include synthetic lubricating oils such as silicone oil, polyalkylene glycol, fluorine oil, and polyα-olefin, and solid lubricants such as molybdenum disulfide and graphite. As the silicone oil, for example, dimethyl silicone oil (for example, Shin-Etsu Chemical Co., Ltd.)
KF-96), phenylmethyl silicone oil (e.g. Molycote 33, manufactured by Dow Corning)
etc. Examples of the polyalkylene glycol include polyoxypropylene glycol monoether (for example, Newpol LB625 manufactured by Sanyo Chemical Industries, Ltd.), polyoxyalkylene derivatives (for example, Unilube manufactured by Nippon Oil & Fats Co., Ltd.),
MB38). Examples of the fluorine oil include polychlorotrifluoroethylene (for example, Daifloil 10 manufactured by Daikin Industries, Ltd.).
etc. Examples of the poly-α-olefin include α-olefin oligomers (for example, Lipolube # 4 manufactured by Lion Oil Co., Ltd.). Examples of the molybdenum disulfide include mineral oil paste or synthetic oil-based molybdenum disulfide (eg, Molycote G manufactured by Dow Corning, Molypaste H manufactured by Sumiko Lubricants Co., Ltd.). Further, as the graphite, for example, synthetic oil paste graphite (for example, Nippon Graphite Industries Co., Ltd.)
Piercing oil # 5 ) manufactured by Hitachi Powder Metallurgy Co., Ltd. and graphite oil (Hitasol GO-102) manufactured by Hitachi Powder Metallurgy Co., Ltd. The amount of such a lubricant is preferably 0.1 to 15 parts (by weight, hereinafter the same), more preferably 0.5 to 5 parts, based on the total amount of the heat-fusible ink layer. If the amount of the lubricant used is less than the above range, there will be no effect of preventing penetration or improving releasability, and if it is more than the above range, the applied ink layer will peel off, both of which are undesirable. Such a lubricant is uniformly dispersed in a hot-fusible ink layer and applied onto the substrate. As for the other ingredients forming the heat-fusible ink layer, the usual ingredients for the heat-fusible ink layer can be used as they are, and there are no particular restrictions on their use. Other ingredients forming the hot-melt ink layer include, for example, colorants, binders, petroleum resins, and softeners. The hot-melt ink layer can be formed by hotmel coating a composition comprising the lubricant, colorant, binder, petroleum resin, and softener, or by dispersing the composition in a suitable solvent. It is formed by coating it with solven. As a binder agent, for example, carnauba wax,
Materials that can be easily melted by heat are preferably used, such as waxes such as auriquy wax and microcrystalline wax, or resins such as low molecular weight polyethylene and polyvinyl stearate. As the softener, materials that can be easily melted by heat, such as polyvinyl acetate, polystyrene, styrene-butadiene copolymers, cellulose esters, cellulose ethers, and acrylic resins, are preferably used. As the colorant, various dyes or pigments that have been widely used in the field of copying paper can be used without any particular restrictions. These binder agents, petroleum resins, softeners, and colorants are used in a total amount of 100 parts (parts by weight,
(same below), 5 to 55 copies, 0.5 to 55 copies, respectively
The blending proportions are preferably 10 parts, 5 to 40 parts, and 2 to 25 parts, in which case the heat-melt ink layer formed has very good melt transferability. In the present invention, a heat-sensitive coloring agent may be used as the coloring agent. The heat-sensitive coloring agent consists of a dye precursor that can develop color by reacting with an acid and an organic or inorganic acid that is solid or semi-solid at room temperature.
A substantially colorless or light-colored heat-melting ink layer is formed by uniformly dispersing or dissolving the heat-sensitive color former binder. The heat-melting ink layer obtained using such a heat-sensitive coloring agent is produced by melting the dispersed solid or semi-solid acid by the heat generated from the heating head, and reacting with the dye precursor to form a clear color. form a recorded image. As the dye precursor, various dye precursors such as phenothiazine type, fluoran type, auramine type, triphenylmethane type, and spiropyran type are all suitably used. As the organic or inorganic acid, for example, benzoic acid, tartaric acid, citric acid, salicylic acid, stearic acid, gallic acid, bisphenol A, naphthoic acid, pyrophosphoric acid, metaphosphoric acid, etc. are preferably used. The heat-fusible ink layer in the present invention has a thickness of 15 μm.
Hereinafter, it is preferably used in a range of 2 to 5 μm. If the thickness is greater than the above range, a large amount of thermal energy will be required to transfer the ink layer, and the resolution will deteriorate, which is not preferable. Next, a case where recording is performed using the thermal transfer recording medium of the present invention using the facsimile apparatus shown in FIG. 3 will be described. That is, FIGS. 1 and 2 are schematic explanatory diagrams showing the recording method of the thermal recording medium of the present invention. In FIGS. 1 and 2, reference numeral 5 denotes a thermal recording medium of the present invention comprising a base material 7 and a heat-melting ink layer 8;
6 is a copy sheet, 2 and 3 are each configured by the pinch roller and printing pattern described above,
A heating head in which heating resistive elements are arranged in a matrix of dot elements such as 1 x 7, 5 x 7, 7 x 9, etc., 9 and 10 are terminals for applying pulses to the heating head 3, and 11 is a terminal on the copy sheet. This is a recorded image formed in In FIG. 1, the thermal recording medium 5 is mounted so that its heat-fusible ink layer 8 faces the copy sheet 6, and the base material 7 of the thermal recording medium 5 is in contact with the heating head 3. On the other hand, copy sheet 6
is in contact with pinch roller 2. Note that the copy sheet 6 is ordinary paper. When pulses corresponding to the printing pattern are applied from the terminals 9 and 10, the heating head 3 generates heat from the dots corresponding to the printing pattern. The Joule heat is instantaneously transmitted to the heat-fusible ink layer 8 through the base material 7, and partially melts the ink layer 8 in accordance with the printed pattern. As shown in FIG. 2, when the pulse application ends, the heating head 3, thermal recording medium 5, and copy sheet 6 are separated from each other, and at that time, the portion of the hot melt ink layer that has been melted according to the printing pattern is A printed image 11 that is peeled off from the base material 7 and transferred to the upper surface of the copy sheet 6, following the printing pattern.
form. In this way, pulse application is repeated and recording is performed continuously. In the present invention, a conventionally known heat-sensitive coloring layer may be provided on the surface of the base material 7 on which the heat-melting ink layer 8 is not provided, so that recording and copying onto the copy sheet 6 can be performed simultaneously. Furthermore, another thermal paper may be interposed between the thermal recording medium 5 of the present invention and the heating head 3. The printed image 11 thus formed is clear because the thin paper that is the base material 7 has excellent heat resistance and thermal conductivity, and the heat-melting ink layer 8 has excellent releasability from the base material 7. The resolution is high,
It has an excellent advantage of not having any unevenness or omission, and also has the advantage of being able to quickly melt and transfer the ink layer 8 with less thermal energy, thereby improving the printing speed.
Moreover, since the hot-melt ink layer 8 contains a lubricant, it does not penetrate into the thin paper that is the base material 7, and therefore, the recording medium of the present invention has no risk of contaminating the heating head 3. Therefore, it can be suitably used as a recording medium for thermal facsimiles and thermal printers. Next, the recording medium of the present invention will be explained with reference to Examples and Comparative Examples. Example 1 0.6 parts of dimethyl silicone oil (KF-96 manufactured by Shin-Etsu Chemical Co., Ltd.) was added as a lubricant to 100 parts of a hot-melt ink composition having the following composition, and the mixture was mixed uniformly. It was applied onto a base material (one-time carbon base paper) to obtain a 4.5μ thick heat-melting ink layer. (Components) (Parts) Carnauba wax 45 Petroleum resin 3 Ethyl cellulose 30 Carbon black 22 Example 2 A heat-fusible ink layer was obtained in the same manner as in Example 1, except that the amount of dimethyl silicone oil added was 4.5 parts. Comparative Example 1 A heat-fusible ink layer was obtained in the same manner as in Example 1 except that dimethyl silicone oil was not added. Comparative Example 2 A heat-fusible ink layer was obtained in the same manner as in Example 1, except that the amount of dimethyl silicone oil added was 20 parts. For each of the thermal transfer recording media thus obtained, the ink permeability to the back surface of the substrate and the releasability of the ink layer were examined. That is, the permeability of the ink was determined by coating the ink on the substrate, leaving it for one day at room temperature, and observing whether or not the ink had leached to the back surface of the substrate. In addition, the releasability of the ink layer is the degree to which ink remains in the printed area when printing is performed on plain paper at a speed of 30 characters/second using a thermal printer (Thermal Printer 100 manufactured by Oki Electric Industry Co., Ltd.), that is, whether the ink is completely removed. The presence or absence of residual ink that adhered to the substrate without being transferred was observed. The results of these tests are shown in the table below.
【表】
比較例2でえた熱転写記録媒体はこれをロール
状に巻回するときにインキ層と基材との間に剥離
がみられた。これに対して、実施例1〜2では巻
回時におけるインキ層の剥離がまつたく認められ
なかつた。
また潤滑性剤として、ニユーポールLB625(三
洋化成工業(株)製のポリオキシプロピレングリコー
ルモノエーテル)、ダイフロイル10(ダイキン工業
(株)製のポリクロロトリフルオロエチレン、モリコ
ート(ダウコーニング社製の鉱油ペースト状二硫
化モリブデン)およびピアシングオイル#5(日
本黒鉛工業(株)製の合成油ペースト状黒鉛)をそれ
ぞれ前記実施例1および2と同様にして熱溶融性
インキ層に含有せしめたものについてもインキの
浸透性およびインキ層の剥離性を前記と同様にし
て調べたが、インキの浸透および印字後の残留イ
ンキは認められず、またロール状に巻回したとき
にもインキ層の基材からの剥離は認められなかつ
た。[Table] When the thermal transfer recording medium obtained in Comparative Example 2 was wound into a roll, peeling was observed between the ink layer and the base material. On the other hand, in Examples 1 and 2, no peeling of the ink layer was observed during winding. In addition, as lubricating agents, Newpol LB625 (polyoxypropylene glycol monoether manufactured by Sanyo Chemical Industries, Ltd.), Dyfloil 10 (Daikin Industries, Ltd.)
Polychlorotrifluoroethylene manufactured by Co., Ltd., Molykoat (mineral oil paste molybdenum disulfide manufactured by Dow Corning), and Piercing Oil #5 (synthetic oil paste graphite manufactured by Nippon Graphite Industries Co., Ltd.) were used in the above examples, respectively. In the same manner as in 1 and 2, the ink permeability and peelability of the ink layer were investigated for the ink contained in the hot-melt ink layer, but no ink permeation or residual ink after printing was observed. No peeling of the ink layer from the base material was observed even when the ink layer was wound into a roll.
第1〜2図は本発明の熱転写記録媒体の記録方
法を示す概略説明図、第3図は感熱紙を用いる通
常のフアクシミリ装置の一例を示す概略説明図で
ある。
(図面の主要符号) 5:熱転写記録媒体、
7:基材、8:熱溶融性インキ層。
1 and 2 are schematic explanatory diagrams showing the recording method of the thermal transfer recording medium of the present invention, and FIG. 3 is a schematic explanatory diagram showing an example of a normal facsimile machine using thermal paper. (Main symbols in the drawing) 5: Thermal transfer recording medium,
7: Base material, 8: Hot-melt ink layer.
Claims (1)
の背面から加熱ヘツドで加熱し、該インキ層の加
熱された部位を選択的に受容体に転写して印像を
形成する記録方法に用いる熱転写記録媒体におい
て、前記基材が薄葉紙であり、かつ前記熱溶融性
インキ層に薄葉紙内へのインキの浸透を防止し、
該インキ層の剥離性を向上せしめる潤滑性剤が含
有されてなる熱転写記録媒体。 2 前記潤滑性剤がシリコーンオイル、フツ素油
またはポリアルキレングリコールである特許請求
の範囲第1項記載の記録媒体。 3 前記潤滑性剤が固体潤滑剤である特許請求の
範囲第1項記載の記録媒体。[Scope of Claims] 1. A heat-melting ink layer provided on a substrate is heated with a heating head from the back side of the substrate, and the heated portions of the ink layer are selectively transferred to a receptor to print. In a thermal transfer recording medium used in a recording method for forming an image, the base material is thin paper, and the heat-fusible ink layer prevents ink from penetrating into the thin paper;
A thermal transfer recording medium containing a lubricant that improves the releasability of the ink layer. 2. The recording medium according to claim 1, wherein the lubricant is silicone oil, fluorine oil, or polyalkylene glycol. 3. The recording medium according to claim 1, wherein the lubricant is a solid lubricant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56200394A JPS58101095A (en) | 1981-12-12 | 1981-12-12 | Heat transfer recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56200394A JPS58101095A (en) | 1981-12-12 | 1981-12-12 | Heat transfer recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58101095A JPS58101095A (en) | 1983-06-16 |
JPH0158078B2 true JPH0158078B2 (en) | 1989-12-08 |
Family
ID=16423587
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56200394A Granted JPS58101095A (en) | 1981-12-12 | 1981-12-12 | Heat transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58101095A (en) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6019588A (en) * | 1983-07-13 | 1985-01-31 | Ricoh Co Ltd | Thermal transfer recording type label |
US4626256A (en) * | 1983-07-25 | 1986-12-02 | Dai Nippon Insatsu Kabushiki Kaisha | Image-receiving sheet |
US4927666A (en) * | 1983-07-25 | 1990-05-22 | Dai Nippon Insatsu Kabushiki Kaisha | Image-receiving sheet |
DE3481596D1 (en) * | 1983-07-25 | 1990-04-19 | Dainippon Printing Co Ltd | SHEET FOR USE IN THERMAL TRANSFER PRINTING. |
US5095000A (en) * | 1983-07-25 | 1992-03-10 | Dai Nippon Insatsu Kabushiki Kaisha | Image-receiving sheet |
US5232893A (en) * | 1983-07-25 | 1993-08-03 | Dai Nippon Insatsu Kabushiki Kaisha | Heat transferable image-receiving sheet, heat transfer assembly and heat transfer process |
JPH0630974B2 (en) * | 1984-04-16 | 1994-04-27 | 松下電器産業株式会社 | Transfer material for thermal recording |
JPS6071292A (en) * | 1983-09-28 | 1985-04-23 | Matsushita Electric Ind Co Ltd | Transfer material for thermal recording |
JPS60219095A (en) * | 1984-04-16 | 1985-11-01 | Matsushita Electric Ind Co Ltd | Transfer material for thermal recording |
JPS60174689A (en) * | 1984-02-20 | 1985-09-07 | Matsushita Electric Ind Co Ltd | Transfer material for thermal recording |
US4643917A (en) * | 1983-11-02 | 1987-02-17 | Konishiroku Photo Industry Co., Ltd. | Heat-sensitive transfer recording medium |
JPS60104395A (en) * | 1983-11-11 | 1985-06-08 | Konishiroku Photo Ind Co Ltd | Thermal transfer recording medium |
JPH0611588B2 (en) * | 1983-12-19 | 1994-02-16 | ダイアホイルヘキスト株式会社 | Thermal transfer material |
JPS60178088A (en) * | 1984-02-24 | 1985-09-12 | General Kk | Delay feeding heat-transfer printing medium |
JPS60220792A (en) * | 1984-04-17 | 1985-11-05 | Matsushita Electric Ind Co Ltd | Transfer type thermal recording system |
JPS60220793A (en) * | 1984-04-17 | 1985-11-05 | Matsushita Electric Ind Co Ltd | Transfer medium for thermal recording |
JPS60229795A (en) * | 1984-04-27 | 1985-11-15 | Matsushita Electric Ind Co Ltd | Transfer body for thermal recording |
JPS60229787A (en) * | 1984-04-27 | 1985-11-15 | Matsushita Electric Ind Co Ltd | Transfer body for thermal recording |
JPS60229792A (en) * | 1984-04-27 | 1985-11-15 | Matsushita Electric Ind Co Ltd | Transfer body for thermal recording |
JPS60229794A (en) * | 1984-04-27 | 1985-11-15 | Matsushita Electric Ind Co Ltd | Heat transfer thermal recording method |
JPS60229793A (en) * | 1984-04-27 | 1985-11-15 | Matsushita Electric Ind Co Ltd | Dye transfer body |
JPH0630971B2 (en) * | 1984-05-02 | 1994-04-27 | ダイアホイルヘキスト株式会社 | Thermal transfer material |
JPS60236788A (en) * | 1984-05-10 | 1985-11-25 | Fuji Xerox Co Ltd | Heat transfer recording medium |
US4732815A (en) * | 1984-08-20 | 1988-03-22 | Dai Nippon Insatsu Kabushiki Kaisha | Heat transfer sheet |
JPH07106675B2 (en) * | 1985-05-17 | 1995-11-15 | 松下電器産業株式会社 | Transfer material for thermal recording |
JPH047970Y2 (en) * | 1985-06-25 | 1992-02-28 | ||
JP2777363B2 (en) * | 1987-01-27 | 1998-07-16 | コニカ株式会社 | Thermal transfer recording medium |
DE3741022C3 (en) * | 1987-12-03 | 1994-12-22 | Pelikan Ag | Multilayer, flexible transfer belt |
JP2825229B2 (en) * | 1988-02-05 | 1998-11-18 | 大日本印刷株式会社 | Thermal transfer sheet |
US4857503A (en) * | 1988-05-13 | 1989-08-15 | Minnesota Mining And Manufacturing Company | Thermal dye transfer materials |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52146310A (en) * | 1976-05-26 | 1977-12-06 | Shikoku Paper Mfg | Stencil papter for transfer sheet and its method of production |
-
1981
- 1981-12-12 JP JP56200394A patent/JPS58101095A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52146310A (en) * | 1976-05-26 | 1977-12-06 | Shikoku Paper Mfg | Stencil papter for transfer sheet and its method of production |
Also Published As
Publication number | Publication date |
---|---|
JPS58101095A (en) | 1983-06-16 |
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