JPS60255491A - Laser recording film - Google Patents
Laser recording filmInfo
- Publication number
- JPS60255491A JPS60255491A JP59112311A JP11231184A JPS60255491A JP S60255491 A JPS60255491 A JP S60255491A JP 59112311 A JP59112311 A JP 59112311A JP 11231184 A JP11231184 A JP 11231184A JP S60255491 A JPS60255491 A JP S60255491A
- Authority
- JP
- Japan
- Prior art keywords
- recording
- film
- protective layer
- layer
- recording layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000010410 layer Substances 0.000 claims abstract description 38
- 239000011241 protective layer Substances 0.000 claims abstract description 21
- 239000011230 binding agent Substances 0.000 claims abstract description 14
- 239000010419 fine particle Substances 0.000 claims abstract description 7
- 239000000758 substrate Substances 0.000 claims abstract description 6
- 239000006096 absorbing agent Substances 0.000 claims description 8
- 229920000620 organic polymer Polymers 0.000 claims description 5
- 238000010521 absorption reaction Methods 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 8
- 229910002804 graphite Inorganic materials 0.000 abstract description 6
- 239000010439 graphite Substances 0.000 abstract description 6
- 239000001856 Ethyl cellulose Substances 0.000 abstract description 2
- 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 abstract description 2
- 239000004793 Polystyrene Substances 0.000 abstract description 2
- 229920001249 ethyl cellulose Polymers 0.000 abstract description 2
- 235000019325 ethyl cellulose Nutrition 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 229920002223 polystyrene Polymers 0.000 abstract description 2
- 238000006748 scratching Methods 0.000 abstract 1
- 230000002393 scratching effect Effects 0.000 abstract 1
- 239000010408 film Substances 0.000 description 36
- -1 polyethylene terephthalate Polymers 0.000 description 16
- 239000000203 mixture Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000007639 printing Methods 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000000020 Nitrocellulose Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 150000001450 anions Chemical group 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001220 nitrocellulos Polymers 0.000 description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Chemical compound [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical class FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010017 direct printing Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000012463 white pigment 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
- B41M5/38207—Contact thermal transfer or sublimation processes characterised by aspects not provided for in groups B41M5/385 - B41M5/395
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はレーザー光を利用する記録に適したレーザー記
録用フィルムに関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a laser recording film suitable for recording using laser light.
情報の高速記録あるいは実時間的記録が必要とされる分
野において、レーザー光を利用する方法が近年多(提案
されている。この方法はレーザー光の光エネルギーの強
さ及び解像力を利用するものであり、光吸収性のよい物
質にレーザー光をIll@射し、こわを吸収して加熱さ
れた物質が受像面に蒸着付着して画倖を記録するもので
ある。In fields where high-speed or real-time recording of information is required, many methods have been proposed in recent years that utilize laser light.This method utilizes the optical energy and resolution of laser light. A laser beam is irradiated onto a material with good light absorption, and the heated material absorbs the stiffness and is deposited on the image receiving surface to record an image.
この記録フィルムとしては、熱を吸収するカーボンブラ
ックなどの微粒子およびニトロ七ルロースなどの自己酸
化性結合物質を含有する被覆物質を塗布した記録フィル
ムが提案されている(4?開昭48−45652号)。As this recording film, a recording film coated with a coating material containing fine particles such as heat-absorbing carbon black and an autooxidizing binding substance such as nitro-hetylulose has been proposed (No. 4, No. 48-45652). ).
この記録フィルムはレーザー光を照射してカーボンブラ
ックなどの微粒子を他の記録テープに転移させることに
より、ネガ、ポジの記録が可能となるものである。This recording film enables negative and positive recording by irradiating it with laser light and transferring fine particles such as carbon black to another recording tape.
また、レーザーエネルギーを吸収する粒子。Also particles that absorb laser energy.
自己酸化性結合剤および交叉結合剤または交叉結合可能
な樹脂あるいは非酸化性重合物質ないしは樹脂と組合さ
れた交叉結合剤からなる被覆物質を透明フィルムに塗布
し、これをアルミニウムシートのよう元石版印刷表面と
緊密に接触させ、透明フィルム側からレーザー光を導入
して、被覆物質を選択的に石版印刷表面に転移させ印刷
版を製造する方法が提案されている(特開昭50−10
2402号〕。これらのレーザー 記e 用フィルムは
いずれもニトロセルロースのような自己酸化性結合剤を
利用し、レーザー光によって供給される熱で自己酸化性
結合剤を加熱して、燃焼ないしは噴出させ、カーボンブ
ランクのような熱吸収粒子と樹脂とを搬出し。A coating material consisting of a self-oxidizing binder and a cross-linking agent or a cross-linking agent in combination with a cross-linkable resin or a non-oxidizing polymeric substance or resin is applied to a transparent film, which is then lithographically printed as an aluminum sheet. A method has been proposed for producing a printing plate by selectively transferring the coating substance to the lithographic printing surface by bringing it into close contact with the surface and introducing a laser beam from the side of the transparent film (Japanese Patent Laid-Open No. 1986-1011).
No. 2402]. All of these laser-grade films utilize a self-oxidizing binder such as nitrocellulose, and the heat provided by the laser beam heats the self-oxidizing binder, causing it to burn or eject, forming a carbon blank. Transport the heat-absorbing particles and resin.
フィルム上に無地な領域を残したり、受像面に画1′I
Jを記録するものである。Do not leave a blank area on the film or leave an image 1'I on the image receiving surface.
This is to record J.
しかし、これらのレーザー記録フィルムや像形成プリン
ト板の製造に供する物品のバインダー樹脂には前述した
ようにニトロセルロースのような自己酸化性結合剤が使
用されているために作像中に熱分解により酸性物質が発
生してシステムを腐蝕したり、保存中の安全性が懸念さ
れたり、解像度が悪いという欠点を有していた。However, as mentioned above, self-oxidizing binders such as nitrocellulose are used in the binder resins of articles used in the manufacture of these laser recording films and image-forming printed boards, so they are susceptible to thermal decomposition during image formation. It has the disadvantages of generating acidic substances that corrode the system, raising concerns about safety during storage, and poor resolution.
本発明者らはこれらの欠点を解消すべく鋭意検討した結
果、バインダーとして非自己酸化性バインダーを使用し
、更に熱を吸収する微粒子としてグラファイトを使用す
ることにより高黒化濃度を達成させることができ、さら
に記録に用いるYA(+レーザー光の波長領域で強い吸
収能を有する熱線吸収剤を含有させることにより記録媒
体を紙、印刷版等の転写受像面に転移し易くすることが
できるとともに透明基板上に記録媒体の残査が残らない
ようにすることができ。The inventors of the present invention made extensive studies to solve these drawbacks, and found that it was possible to achieve a high blackening density by using a non-self-oxidizing binder as the binder and graphite as the heat-absorbing fine particles. Furthermore, by containing a heat ray absorber that has strong absorption ability in the wavelength range of YA (+ laser light) used for recording, the recording medium can be easily transferred to the transfer image receiving surface of paper, printing plate, etc., and it is transparent. It is possible to prevent any residue of the recording medium from remaining on the substrate.
尚解像度のネガ、ポジ画像を与えるレーザー記録用フィ
ルムが得られることを見い出し先に特願昭59−417
24号として出願した。In addition, a patent application filed in 1983-417 discovered that it was possible to obtain a laser recording film that gave high-resolution negative and positive images.
The application was filed as No. 24.
しかしながら、さらに検討した結果この様な記録層(記
録媒体層)はそれ自体傷が付き易く。However, further study revealed that such a recording layer (recording medium layer) itself is easily scratched.
又乾燥塗膜厚味が約0.5μm と薄いため、傷は記録
層の表面だけでなく、基板の表面にまで容易に到達する
。このような傷はレーザ二足碌用フィルムとしての機能
を著しく損うものである。Furthermore, since the dry coating film thickness is as thin as about 0.5 μm, scratches easily reach not only the surface of the recording layer but also the surface of the substrate. Such scratches significantly impair the function of the film for laser bipedal use.
本発明者らはこのような欠点′に解消すべく鋭意検討し
た結果、透明基板上の記録層の表面に有機高分子からぬ
る保護層を設けることにょp。The inventors of the present invention have made extensive studies to overcome these drawbacks, and have decided to provide a protective layer made of organic polymer on the surface of the recording layer on the transparent substrate.
従来のレーザー記録用フィルムに比べて著しい耐擦傷性
を有するレーザ二足碌用フィルムが得られることを見い
出し本発明に到達した。The present inventors have discovered that a laser recording film with remarkable scratch resistance compared to conventional laser recording films can be obtained, and have thus arrived at the present invention.
即ち1本発明は透明な基板上に、非自己酸化性バインダ
ーと、高黒化濃度を賦与し熱を吸収する微粒子と、記録
に用いるレーザー光の波長領域で強い吸収能を有する熱
線吸収剤とを含有する記録層を設けたレーザー記録用フ
ィルムにおいて該記録層の上に有機高分子からなる保護
層を設けたこと全特徴とするレーザー記録用フィルムを
提供するものである。That is, 1. the present invention comprises, on a transparent substrate, a non-self-oxidizing binder, fine particles that provide high blackening density and absorb heat, and a heat ray absorber that has strong absorption ability in the wavelength range of laser light used for recording. The object of the present invention is to provide a laser recording film provided with a recording layer containing the present invention, which is characterized in that a protective layer made of an organic polymer is provided on the recording layer.
本発明になるレーザー記録用フィルムの構成は第1図に
示すように、レーザー光透過性の支持体1上に、非自己
酸化性バインダーと、高黒化濃度を賦与し、熱を吸収す
る微粒子と、記録に用いるレーザー光の波長領域で強い
吸収能を有する熱線吸収剤とを含有させた記録媒体を塗
布した層(記録層)2.さらに記録層2上に有機高分子
で形成された保護層5を設けてなる。The structure of the laser recording film according to the present invention is as shown in FIG. A layer (recording layer) coated with a recording medium containing: Furthermore, a protective layer 5 made of an organic polymer is provided on the recording layer 2.
記録の方法としては第2図に示すよう九通常のレンズ系
及び調整装f[−通して調節したレーザー光を支持体1
の側から走査して導き、記録層(転写供給体)2t−転
写受像体4の受像面に蒸着付着させて画像を記録する方
法を用いることができる。受像面は保護層3と接触させ
て装清することが望ましく、減圧操作により密着度を向
上させると解像度はいっそう良好となる。As shown in Fig. 2, the recording method is as shown in Figure 2.
A method can be used in which the image is recorded by scanning and guiding from the recording layer (transfer supply body) 2t to the image receiving surface of the transfer image receptor 4 by vapor deposition. It is desirable that the image-receiving surface be in contact with the protective layer 3 for cleaning, and if the degree of adhesion is improved by reducing the pressure, the resolution will be even better.
この方法によると、1回の操作で転写受像体4上にポジ
像、記録層2上にネガ像上同時に得ることができる。ネ
ガフィルムは印刷樹脂刷版作成時に利用でき、ポジ像は
転写受像体4の種類によシ校正用フビーあるいは直接刷
版として使用できる。According to this method, a positive image on the transfer image receptor 4 and a negative image on the recording layer 2 can be simultaneously obtained in one operation. The negative film can be used when making a printing resin printing plate, and the positive image can be used as a proofing film or a direct printing plate depending on the type of transfer image receptor 4.
本発明のレーザー記録用フィルムの支持体としては、レ
ーザー光を透過するフィルムであればよ<、ポリスチレ
ンフィルム、ポリエチレンテレフタレートフィルム等が
挙げられる。The support for the laser recording film of the present invention may be any film that transmits laser light, such as polystyrene film, polyethylene terephthalate film, and the like.
記録層中の熱を吸収し、高黒化濃度を達成させる微粒子
としてはグラファイト、カーボンブランク等を挙げるこ
とができ、単独もしくは混合物として使用できる。特に
、薄膜で高黒化濃度を賦与できるものとしては、微粉末
グラファイトがよい。Examples of fine particles that absorb heat in the recording layer and achieve high blackening density include graphite and carbon blank, which can be used alone or as a mixture. In particular, fine powder graphite is preferred as a material capable of imparting a high blackening density in a thin film.
記録層中のレーザー光の波長領域で強い吸収能を有する
熱線吸収剤としては、例えば、下記の一般式(11ある
いは(II)で示される化合物が挙げられる。Examples of the heat ray absorber having a strong absorption ability in the laser beam wavelength region in the recording layer include compounds represented by the following general formula (11 or (II)).
一般式(I)
(ここで、Rは水素又は低級アルキル基、Xはへキサフ
ルオロヒ酸イオン、ヘキサフルオロアンチモン酸イオン
、フッ化ホウ素酸イオンおよび過塩素酸イオンよりなる
群から選ばれる陰イオンであり1mは0まkは1.2の
整数である。Aは÷Cへまたは=O=を示す。ンこの一
般式(I+で示されるものの例としてはN。General formula (I) (wherein, R is hydrogen or a lower alkyl group, and X is an anion selected from the group consisting of hexafluoroarsenate ion, hexafluoroantimonate ion, fluoroborate ion, and perchlorate ion) 1m is 0 and k is an integer of 1.2.A indicates ÷C or =O=.
N、N’N/−テトラキス(p−ジェチルアミノフェニ
ルンーp−アミノフェニルアミウムのへギサシルオロア
ンチモン酸塩、ヘキサフルオロヒ酸塩、過塩素酸塩或い
はフン化ホウ素酸塩、 N、N。N. ,N.
N′、N′−テトラキス(p−ジブチルアミノフェニル
)−p−アミノフェニルアミラムのヘキサフルオロアン
チモン酸塩、へ、キサフルオロヒ11m。Hexafluoroantimonate of N',N'-tetrakis(p-dibutylaminophenyl)-p-aminophenyl amylam, hexafluorohyde 11m.
過塩素酸塩或いはフッ化ホウ素m塩、 N、N、N−、
NI−テトラキス(p−ジエチルアミノフェニル)−p
−ベンゾキノン−ビスイモニウムのヘキサフルオロアン
チモン酸塩、ヘキサフルオロヒ酸塩、過壇索酸塩或いは
フッ化ホク累酸壌、 N、N。Perchlorate or boron fluoride salt, N, N, N-,
NI-tetrakis(p-diethylaminophenyl)-p
- benzoquinone-bisimonium hexafluoroantimonate, hexafluoroarsenate, persodium salt or fluorinated acid salt, N,N.
Nl、NI−テトラキス(p−ジプロピルアミノフェニ
ル)−p−ベンゾフェノン−ビスイモニウムのヘキサフ
ルオロアンチモン酸塩、ヘキサフルオロヒ酸塩、過塩素
酸塩或いはフン化ホウ素酸塩などがある。Examples include hexafluoroantimonate, hexafluoroarsenate, perchlorate, and fluoroborate of Nl, NI-tetrakis(p-dipropylaminophenyl)-p-benzophenone-bisimmonium.
一般式(II)
バ3
(ここで%R1およびR2は同じかまたは異なるアルキ
ル基t−,R,は水素、アルキル、フェニル、ベンジル
基を1mは+1または+2の整数を、Lはmが+1のと
き1価のアニオンであり。General formula (II) B3 (%R1 and R2 are the same or different alkyl groups t-, R, is hydrogen, alkyl, phenyl, benzyl group, 1m is an integer of +1 or +2, L is m is +1 When , it is a monovalent anion.
またmが+2のとき2価のアニオンを示す。)この一般
式(II)で示されるものの例としてはビス(p−ジエ
チルアミノフェニル) (NtN−ビス(p−ジエチル
アミノフェニル)−4’−7ミ/ビフエニル〕アミニウ
ムヘキサフルオロアンチモネートがある。Further, when m is +2, it indicates a divalent anion. ) An example of the compound represented by the general formula (II) is bis(p-diethylaminophenyl)(NtN-bis(p-diethylaminophenyl)-4'-7mi/biphenyl)aminium hexafluoroantimonate.
記録層中の非自己酸化性バインダーとしてはアクリル系
樹脂、ニトロセルロースt−除<七ルロース誘導体、フ
ェノール樹脂、ポリ塩化ビニル、塩化ビニル−酢酸ビニ
ル共重合体等を使用できる。非自己酸化性バインダーを
使用することにより、ニトロ士ルロースの様な自己酸化
性バインダーの保存中の安全性の懸念やレーザー光照射
時に発生する酸性物質による装置の腐食に関する問題は
全くな(なった。As the non-self-oxidizing binder in the recording layer, acrylic resins, nitrocellulose t-lulose derivatives, phenolic resins, polyvinyl chloride, vinyl chloride-vinyl acetate copolymers, etc. can be used. By using a non-auto-oxidizing binder, there are no concerns about the safety of auto-oxidizing binders such as nitrosylulose during storage, and there are no problems with equipment corrosion due to acidic substances generated during laser light irradiation. .
記録層の黒化濃度は0.5以上で望ましくは2.0以上
である。黒化濃度が低いとネガフィルムとしての遮光性
能に劣り、ポジ画像としても薄い印字となる。The blackening density of the recording layer is 0.5 or more, preferably 2.0 or more. If the blackening density is low, the light-shielding performance as a negative film will be poor, and even a positive image will have a weak print.
熱線吸収剤の添加量は非自己酸化性バインダー100重
量部に対して0.01へ200M量部。The amount of the heat ray absorber added was 0.01 to 200 M parts per 100 parts by weight of the non-self-oxidizing binder.
特に0.1〜100重量部の範囲が好ましい。Particularly preferred is a range of 0.1 to 100 parts by weight.
熱線吸収剤の添加は特にネガフィルム(転写供給体)の
記録層の転移に大きく影響を及ぼし。The addition of a heat ray absorber has a great effect on the transfer of the recording layer of a negative film (transfer supply body) in particular.
解像度を上げる効果が顕著である。無添加の場合には記
録層の転移により抜けた部分に残置が残カ易いが、これ
をほとんど無くすことができ。The effect of increasing resolution is remarkable. In the case of no additive, it is easy to leave a residue in the part where the recording layer is transferred, but this can be almost completely eliminated.
樹脂製版用ネガフィルム作成の場合には特に効果的であ
る。This is particularly effective when creating a negative film for resin plate making.
記録層および保護層の厚味は使用するレーザー光のパワ
ー及び黒化濃度と熱線吸収剤の添加量にも影響を受ける
が、記碌l−1保護層合わせて、0.1〜1.0μの範
囲がよ(、好ましくは0.2〜0.7μが良い。The thickness of the recording layer and the protective layer is affected by the power of the laser beam used, the blackening density, and the amount of heat ray absorber added, but the thickness of the recording layer and the protective layer is 0.1 to 1.0μ in total. The range of (preferably 0.2 to 0.7μ) is good.
保護層を記録層に傷が全く付かないほど十分な膜厚例え
ば約0.5μ以上に形成すると、レーザーによる記録感
度が大幅に減少する。When the protective layer is formed to a thickness sufficient to prevent any scratches on the recording layer, for example, approximately 0.5 μm or more, the recording sensitivity by laser is significantly reduced.
本発明で保護層として用いられる有機高分子としては機
械的強度のある各種の高分子物質を用いることができる
が、記録層の上に保護層の塗布液を塗布する際、その液
は記録層を溶解させて破壊したり変化させるものであっ
てはならない。よって記録層および保護層の塗布液の溶
剤は限定され、又塗布すべき物質も限定される。Various types of mechanically strong polymer substances can be used as the organic polymer used as the protective layer in the present invention, but when applying the coating liquid for the protective layer on the recording layer, the liquid It must not dissolve or destroy or change. Therefore, the solvents for the coating liquids for the recording layer and the protective layer are limited, and the substances to be coated are also limited.
溶剤に対して抵抗力の少ない記録層の場合には。In the case of a recording layer that is less resistant to solvents.
水溶性高分子例えばポリビニルアルコール、ボリアクリ
ルアばドウポリビニルピロリドン、ポリアクリル酸、カ
ルボキシメチルセルロース。Water-soluble polymers such as polyvinyl alcohol, polyacrylic acid, polyvinylpyrrolidone, polyacrylic acid, and carboxymethylcellulose.
デン粉、カゼイン等の水溶液、塩化ビニルと酢酸ビニル
の共重合体、ポリ塩化ビニル、ポリ塩化ビニリデン、ポ
リウレタン、ポリエチレン。Aqueous solutions of starch, casein, etc., copolymers of vinyl chloride and vinyl acetate, polyvinyl chloride, polyvinylidene chloride, polyurethane, polyethylene.
カルボキシル化ポリエチレン等の水性分散液を用いるこ
とにより、保護層を形成することができる。A protective layer can be formed by using an aqueous dispersion of carboxylated polyethylene or the like.
転写受像体としては、一般紙、グラスチックフィルム、
合成紙(白色顔料をプラスチックフィルム中に分散した
もの)、陽極酸化したアルミニウム等が使用される。Transfer image receptors include general paper, glass film,
Synthetic paper (white pigment dispersed in plastic film), anodized aluminum, etc. are used.
一般紙、プラスチックフィルム、合成紙等を使用した場
合には校正用コピー、印刷物として利用でき、陽極酸化
したアルミニウム全使用した場合には転写像をそのま〜
あるいはゴムライニングして刷版として利用できる。When using general paper, plastic film, synthetic paper, etc., it can be used as a proof copy or printed matter, and when using entirely anodized aluminum, the transferred image can be used as is.
Alternatively, it can be lined with rubber and used as a printing plate.
本発明になるレーザー記録用フィルムは、現象定着など
の後処理を必要としない來時間記録であp、さらに感光
しないので暗室操作が不袂であり、近年急速に発展して
いる通信、コンピューター処理情報を直接記録するのに
最適であり、広く応用することが可能である。The laser recording film of the present invention is a recording film that does not require post-processing such as phenomenon fixing, and is not exposed to light, making it difficult to operate in a dark room. It is ideal for directly recording information and can be widely applied.
以下1本発明を実施例をもって説明する。実施例中の部
はすべて重量部を表わす。The present invention will be explained below with reference to examples. All parts in the examples represent parts by weight.
実施例1
下記グラファイト分散液(処方1〕中に熱線吸収剤とし
てアメリカン・サイアナミツド・ケミカル社製0yas
orb I R−126f 1.5部添加した配合液を
バーコードにより75μポリエステルフイルム上に塗工
し、乾燥させ、記録層を形成させた。この記録層上に処
方2からなる配合液を塗布し、保護層を形成させた。乾
燥皮膜厚味、黒化濃度、耐擦傷性試験結果、およびYA
Gレーザ−(波長11060n、出力10W、記録媒体
上0.s 、rou1/rs2)照射による作像試験結
果をまとめて表1に示す。Example 1 0yas manufactured by American Cyanamid Chemical Co. was used as a heat ray absorber in the following graphite dispersion (formulation 1).
A blended solution containing 1.5 parts of orb I R-126f was applied onto a 75μ polyester film using a bar code and dried to form a recording layer. A liquid mixture consisting of Formulation 2 was applied onto this recording layer to form a protective layer. Dry film thickness, blackening density, scratch resistance test results, and YA
Table 1 summarizes the results of an image forming test using G laser (wavelength 11060n, output 10W, 0.s above the recording medium, rou1/rs2) irradiation.
処方1 グラファイト 100部
エチルセルロース 58部
イングロビルアルコール 1170部
処方2 ポリビニルアルコール
水 96部
笑施例2
!J!施例1で塗布した記録層上に処方5からなる塗工
液金塗布し、保護層を形成させた。乾燥皮膜厚味、黒化
濃度、耐擦傷性試験結果およびYAGレーザ−(波長1
1060n、出力10W。Formula 1 Graphite 100 parts Ethyl cellulose 58 parts Inglobil alcohol 1170 parts Formula 2 Polyvinyl alcohol water 96 parts Example 2! J! On the recording layer coated in Example 1, a coating liquid gold consisting of Formulation 5 was applied to form a protective layer. Dry film thickness, blackening density, scratch resistance test results and YAG laser (wavelength 1
1060n, output 10W.
記録媒体上0,5 JOul/1)12) [1躬によ
る作像試験結果をまとめて表1に示す。−
処方5 アクリル系エマルジョン 5部水 10部
実施例5
実施例1で塗布した記録層上に処方4からなる塗工液を
塗布し、保護層を形成させた。乾燥皮膜厚味、黒化濃度
、耐擦傷性試験結果およびYAGレーザ−(波長110
60n、出力10W。On the recording medium 0.5 JOul/1) 12) [1] The results of the image forming test are summarized in Table 1. - Formulation 5 Acrylic emulsion 5 parts Water 10 parts Example 5 A coating liquid consisting of Formulation 4 was applied onto the recording layer applied in Example 1 to form a protective layer. Dry film thickness, blackening density, scratch resistance test results and YAG laser (wavelength 110
60n, output 10W.
記録媒体上0.5 Jou1/鋤2)服射による作像試
験結果をまとめて表1に示す。Table 1 summarizes the results of the image forming test using 0.5 Jou1/Plow2) exposure on the recording medium.
処方4 ポリアクリルアミド 4部
水 6部
実施例4
実施例1で塗布した記録層上に処方5からなる塗工液を
塗布し、保護層を形成させた。乾燥皮膜厚味、黒化濃度
、耐擦傷性試験結果、およびYAGレーザ−(波長11
060n、出力10W、記録媒体上0.5 Joul/
(至)2)照射による作像試験結果をまとめて表1に示
す。Formulation 4 Polyacrylamide 4 parts Water 6 parts Example 4 A coating liquid consisting of Formulation 5 was applied onto the recording layer applied in Example 1 to form a protective layer. Dry film thickness, blackening density, scratch resistance test results, and YAG laser (wavelength 11
060n, output 10W, 0.5 Joul/on recording medium
(To) 2) Table 1 summarizes the results of the image formation test by irradiation.
処方5 アクリル系エマルジョン 1部水 10部
比較例1
実施例1において、処方1のみを塗布したフィルムを比
較例として用いた。Formulation 5 Acrylic emulsion 1 part water 10 parts Comparative Example 1 In Example 1, a film coated with only Formulation 1 was used as a comparative example.
(注*2)実施例、比較例の耐擦傷性は次の方法によっ
た。(Note*2) The scratch resistance of Examples and Comparative Examples was determined by the following method.
第5図に示す如く、支持体1.記録層2及び保護層5か
らなるフィルムを101)lIXlo−に切り、塗布面
に、断面積1偏2 の紙片5ft置き。As shown in FIG. 5, support 1. A film consisting of the recording layer 2 and the protective layer 5 was cut into 101) lIXlo- pieces, and 5 ft of paper strips each having a cross-sectional area of 1 sq 2 were placed on the coated surface.
荷重6をかけながら、水平方向に約5am移動させる。While applying a load of 6, move about 5 am in the horizontal direction.
その後、移動させた部分の傷の有無を確認する。荷重を
変化させながら行い、記録層に傷の付いた時の荷重の値
を下記の基準でその保護層の耐擦傷性の評価とした。After that, check whether there are any scratches on the moved part. The test was carried out while changing the load, and the value of the load when the recording layer was scratched was evaluated as the scratch resistance of the protective layer using the following criteria.
Aニア50Ji’の荷重で記録層に傷が付かない。The recording layer is not damaged by the load of A Near 50Ji'.
B:5009の荷重で記録層に傷が付かない。B: The recording layer is not scratched under a load of 5009.
o: soyの荷重で記録層に傷が付く。o: The recording layer is scratched by the soy load.
第1図は本発明のレーザー記録用フィルムの断面図、第
2図は本発明のフィルムを用いた記録装置の略示断面図
、第5図は耐擦傷性試験の測定方法を示す図である。
1・・・支持体、2・・・記録層、5・・・保護層、4
・・・転写受像体。
第1図
第2図FIG. 1 is a cross-sectional view of a laser recording film of the present invention, FIG. 2 is a schematic cross-sectional view of a recording device using the film of the present invention, and FIG. 5 is a diagram showing a measuring method for a scratch resistance test. . DESCRIPTION OF SYMBOLS 1... Support body, 2... Recording layer, 5... Protective layer, 4
...Transfer image receptor. Figure 1 Figure 2
Claims (1)
化濃度を賦与し熱を吸収する微粒子と、記録に用いるレ
ーザー光の波長領域で強い吸収能を有する熱線吸収剤と
を含有する記録層を設けたレーザー記録用フィルムにお
いて、該記録層の上に有機高分子からなる保護層を設け
たことを特徴とするレーザー記録用フィルム。1. Recording containing, on a transparent substrate, a non-self-oxidizing binder, fine particles that provide high blackening density and absorb heat, and a heat ray absorber that has strong absorption ability in the wavelength range of the laser light used for recording. 1. A laser recording film comprising a layer, characterized in that a protective layer made of an organic polymer is provided on the recording layer.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59112311A JPS60255491A (en) | 1984-06-01 | 1984-06-01 | Laser recording film |
PCT/JP1985/000305 WO1985005595A1 (en) | 1984-06-01 | 1985-05-31 | Film for laser recording |
GB08601877A GB2176018B (en) | 1984-06-01 | 1985-05-31 | Film for laser recording |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59112311A JPS60255491A (en) | 1984-06-01 | 1984-06-01 | Laser recording film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60255491A true JPS60255491A (en) | 1985-12-17 |
Family
ID=14583498
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59112311A Pending JPS60255491A (en) | 1984-06-01 | 1984-06-01 | Laser recording film |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPS60255491A (en) |
GB (1) | GB2176018B (en) |
WO (1) | WO1985005595A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61192737A (en) * | 1985-02-05 | 1986-08-27 | チバ・ガイギー・アクチエンゲゼルシヤフト | Marking method for pigment system by laser |
JPS62234991A (en) * | 1986-04-04 | 1987-10-15 | Daicel Chem Ind Ltd | Laser recording film |
JPS62249788A (en) * | 1986-04-24 | 1987-10-30 | Daicel Chem Ind Ltd | Film for laser recording |
JPH01160683A (en) * | 1987-11-20 | 1989-06-23 | Eastman Kodak Co | Near infrared absorbing dyestuff for heat transfer |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60262687A (en) * | 1984-06-11 | 1985-12-26 | Daicel Chem Ind Ltd | Laser recording film |
DE3710183A1 (en) * | 1987-03-27 | 1988-10-13 | Siemens Ag | DEVICE FOR LASER TRANSFER PRINTING |
DE3730842C2 (en) * | 1987-09-14 | 1999-02-25 | Eastman Kodak Co | Ribbon for a device for laser transfer printing |
US5171650A (en) * | 1990-10-04 | 1992-12-15 | Graphics Technology International, Inc. | Ablation-transfer imaging/recording |
DK0465562T4 (en) * | 1989-03-30 | 2000-04-17 | Polaroid Corp | Near Infrared Laser Absorbent Coating and Method for Use in Color Imaging and Imprinting |
FR2654982B1 (en) * | 1989-11-29 | 1992-03-06 | Merlin Gerin | LASER MARKING PROCESS AND PAINT. |
EP0419377B2 (en) * | 1989-09-22 | 2001-04-18 | Schneider Electric Sa | Procedure apparatus and paint for the laser marking of castings for electrical apparatus |
US5278023A (en) * | 1992-11-16 | 1994-01-11 | Minnesota Mining And Manufacturing Company | Propellant-containing thermal transfer donor elements |
EP0678200B1 (en) * | 1992-11-18 | 2002-02-27 | PGI Graphics Imaging LLC | On-demand production of lat imaging films |
US6756181B2 (en) | 1993-06-25 | 2004-06-29 | Polyfibron Technologies, Inc. | Laser imaged printing plates |
DE69425943T2 (en) * | 1993-11-05 | 2001-04-12 | Vari Lite Inc | Light pattern template and laser ablation process or device for their production |
US5429909A (en) * | 1994-08-01 | 1995-07-04 | Eastman Kodak Company | Overcoat layer for laser ablative imaging |
US5819661A (en) * | 1995-01-23 | 1998-10-13 | Presstek, Inc. | Method and apparatus for laser imaging of lithographic printing members by thermal non-ablative transfer |
US5945249A (en) | 1995-04-20 | 1999-08-31 | Imation Corp. | Laser absorbable photobleachable compositions |
GB9617416D0 (en) * | 1996-08-20 | 1996-10-02 | Minnesota Mining & Mfg | Thermal bleaching of infrared dyes |
US5935758A (en) | 1995-04-20 | 1999-08-10 | Imation Corp. | Laser induced film transfer system |
US5506086A (en) * | 1995-05-01 | 1996-04-09 | E. I. Du Pont De Nemours And Company | Process for making a flexographic printing plate |
US5747217A (en) * | 1996-04-03 | 1998-05-05 | Minnesota Mining And Manufacturing Company | Laser-induced mass transfer imaging materials and methods utilizing colorless sublimable compounds |
US5691098A (en) * | 1996-04-03 | 1997-11-25 | Minnesota Mining And Manufacturing Company | Laser-Induced mass transfer imaging materials utilizing diazo compounds |
JPH10148939A (en) * | 1996-11-18 | 1998-06-02 | Konica Corp | Image forming material and its production |
US6168903B1 (en) | 1999-01-21 | 2001-01-02 | Presstek, Inc. | Lithographic imaging with reduced power requirements |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4843632A (en) * | 1971-09-30 | 1973-06-23 | ||
JPS5948188A (en) * | 1982-09-13 | 1984-03-19 | Fuji Xerox Co Ltd | Transfer type heat-sensitive recording medium |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5188016A (en) * | 1975-01-29 | 1976-08-02 | ||
JPS5714096A (en) * | 1980-06-30 | 1982-01-25 | Pentel Kk | Laser heatsensitive recording material |
JPS5714095A (en) * | 1980-06-30 | 1982-01-25 | Pentel Kk | Laser-heatsensitive copy recording sheet |
JPS5777590A (en) * | 1980-11-01 | 1982-05-14 | Konishiroku Photo Ind Co Ltd | Image recording method |
EP0113167A3 (en) * | 1982-10-14 | 1986-06-18 | Autotype International Limited | Laser imaging materials |
GB8410515D0 (en) * | 1984-04-25 | 1984-05-31 | Ici Plc | Laser-imageable assembly |
GB8410514D0 (en) * | 1984-04-25 | 1984-05-31 | Ici Plc | Laser-imageable assembly |
-
1984
- 1984-06-01 JP JP59112311A patent/JPS60255491A/en active Pending
-
1985
- 1985-05-31 WO PCT/JP1985/000305 patent/WO1985005595A1/en unknown
- 1985-05-31 GB GB08601877A patent/GB2176018B/en not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4843632A (en) * | 1971-09-30 | 1973-06-23 | ||
JPS5948188A (en) * | 1982-09-13 | 1984-03-19 | Fuji Xerox Co Ltd | Transfer type heat-sensitive recording medium |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61192737A (en) * | 1985-02-05 | 1986-08-27 | チバ・ガイギー・アクチエンゲゼルシヤフト | Marking method for pigment system by laser |
JPS62234991A (en) * | 1986-04-04 | 1987-10-15 | Daicel Chem Ind Ltd | Laser recording film |
JPS62249788A (en) * | 1986-04-24 | 1987-10-30 | Daicel Chem Ind Ltd | Film for laser recording |
JPH01160683A (en) * | 1987-11-20 | 1989-06-23 | Eastman Kodak Co | Near infrared absorbing dyestuff for heat transfer |
JPH0529558B2 (en) * | 1987-11-20 | 1993-04-30 | Eastman Kodak Co |
Also Published As
Publication number | Publication date |
---|---|
GB2176018A (en) | 1986-12-10 |
GB8601877D0 (en) | 1986-03-05 |
GB2176018B (en) | 1988-05-25 |
WO1985005595A1 (en) | 1985-12-19 |
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