JPH01282399A - Recording sheet - Google Patents
Recording sheetInfo
- Publication number
- JPH01282399A JPH01282399A JP63110466A JP11046688A JPH01282399A JP H01282399 A JPH01282399 A JP H01282399A JP 63110466 A JP63110466 A JP 63110466A JP 11046688 A JP11046688 A JP 11046688A JP H01282399 A JPH01282399 A JP H01282399A
- Authority
- JP
- Japan
- Prior art keywords
- ink
- recording sheet
- resin
- glass transition
- transition temperature
- 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 20
- 239000002344 surface layer Substances 0.000 claims abstract description 19
- 239000011347 resin Substances 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 230000009477 glass transition Effects 0.000 claims abstract description 12
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 10
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229920001577 copolymer Polymers 0.000 claims abstract description 7
- 229920001519 homopolymer Polymers 0.000 claims abstract description 5
- 229920000642 polymer Polymers 0.000 claims abstract description 5
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims abstract description 4
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 claims abstract description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000428 dust Substances 0.000 abstract description 7
- 239000002985 plastic film Substances 0.000 abstract description 7
- 239000000178 monomer Substances 0.000 abstract description 5
- 238000010030 laminating Methods 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 abstract 2
- 238000000576 coating method Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- -1 polyethylene terephthalate Polymers 0.000 description 6
- 229920006255 plastic film Polymers 0.000 description 5
- 125000005395 methacrylic acid group Chemical class 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229920002160 Celluloid Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 238000007754 air knife coating Methods 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 238000007611 bar coating method Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- XLIDPNGFCHXNGX-UHFFFAOYSA-N dialuminum;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Si+4] XLIDPNGFCHXNGX-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000197 polyisopropyl acrylate Polymers 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000182 polyphenyl methacrylate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
-
- 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
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明はインクリボンを使用するワイヤドツトプリンタ
ーに好適な記録シートに関し、より詳細にはインク受容
性に優れた記録シートに関するものである。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a recording sheet suitable for a wire dot printer using an ink ribbon, and more particularly to a recording sheet with excellent ink receptivity.
〈従来の技術〉
ワイヤドツトプリンターは、現在量も一般的なプリンタ
ーのうちのひとつであり、広(一般に普及している。こ
のプリンターに使用されるインクは、ワックス系の物質
をバインダーとして染料や顔料の色材が分散されたもの
であり、印字された際に記録紙表面の凹凸にワックス系
物質が打ち込まれることによって定着せしめるものであ
る。<Prior art> Wire dot printers are one of the most common printers available today, and are widely used. It is a dispersion of pigment coloring material, and when printed, a wax-based substance is driven into the irregularities on the surface of the recording paper to fix it.
しかし、近年になって記録媒体の多様化に伴ってワイヤ
ドツトプリンターにおいても各種プラスチックフィルム
、合成繊維シート、金属蒸着シート等の従来の紙とは興
なった特殊シート状物へのプリントが望まれる様になっ
てきたが、これらのシート状物は表面の凹凸が全くない
か、あっても非常に少ないため、印字が適正に行われて
もインクの定着状態が十分に得られずに、指先でこすっ
た程度でインクが落ちてしまったり、他のものに転写し
てしまったりという問題があった。However, in recent years, with the diversification of recording media, it has become desirable for wire dot printers to be able to print on special sheet-like materials that are different from conventional paper, such as various plastic films, synthetic fiber sheets, and metallized sheets. However, these sheet-like materials have no or very few surface irregularities, so even if printing is done properly, the ink cannot be fixed properly, and the surface is rough. There was a problem in that the ink would fall off or be transferred to other objects even if rubbed with a brush.
また、従来から使用されている記録紙の場合、紙そのも
のの性質上紙粉の発生は抑える事ができず、クリーンル
ーム内の様に塵、埃等が問題となる環境下での使用には
適さず、紙に代わる紙粉等の発生しない記録シートの要
望がある。この様な要望に対してプラスチックフィルム
等のシートは紙粉の問題は解消されるものの、上記した
如(インク定着性の問題があり、クリーンルーム等の環
境下での実用上問題のない記録シートが要望されている
。In addition, in the case of conventionally used recording paper, the generation of paper dust cannot be suppressed due to the nature of the paper itself, and it is not suitable for use in environments where dust and dust are a problem, such as in a clean room. First, there is a demand for a recording sheet that does not generate paper dust or the like as an alternative to paper. In response to these demands, sheets such as plastic film solve the problem of paper dust, but as mentioned above (there is a problem with ink fixation), recording sheets that do not have any practical problems in environments such as clean rooms are not available. It is requested.
一方、上記の如きプラスチックフィルムのインク定着性
を改善すべく、表面に顔料粒子を多く含有した表面層を
設ける方法も提案されているが、顔料の脱落とか、外観
が悪いとか、特にオーバーヘッドプロジェクタ−用には
透明性が損なわれてしまうという問題があり、従ってワ
イヤドツトプリンター用として十分に満足される品質の
フィルムタイプの記録シートは未だ得られていない状況
である。On the other hand, in order to improve the ink fixation properties of plastic films such as those mentioned above, a method of providing a surface layer containing a large amount of pigment particles on the surface has been proposed, but there are problems such as falling off of the pigment and poor appearance, especially for overhead projectors. There is a problem in that transparency is impaired when used for wire dot printers, and therefore, a film-type recording sheet of sufficiently satisfactory quality for use in wire dot printers has not yet been obtained.
〈発明が解決しようとする課題〉
本発明は上記の如き事情に鑑み、インク定着性に優れた
、紙粉等のダストが発生しないワイヤドットプリ−ンタ
ーによる印字に好適な記録シートを提供するものである
。<Problems to be Solved by the Invention> In view of the above circumstances, the present invention provides a recording sheet suitable for printing with a wire dot printer, which has excellent ink fixing properties and does not generate dust such as paper powder. It is.
〈課題を解決するための手段〉
本発明は、支持体上の少なくとも片面にガラス転移温度
が20℃以下のアクリル系樹脂を主成分とするインク受
容層、及びガラス転移温度が80℃以上の樹脂を主成分
とする表面層を順次積層したことを特徴とする記録シー
トである。<Means for Solving the Problems> The present invention provides an ink receiving layer mainly composed of an acrylic resin having a glass transition temperature of 20° C. or lower on at least one side of a support, and a resin having a glass transition temperature of 80° C. or higher. This is a recording sheet characterized by sequentially laminating surface layers containing as a main component.
本発明の記録シートを構成するインク受容層は、記録時
に記録手段からインクを受容して定着する部分であり、
ガラス転移温度(以下Tgと称す)が20℃以下のアク
リル系樹脂を主成分としで含有するものである。The ink-receiving layer constituting the recording sheet of the present invention is a part that receives ink from a recording means and fixes it during recording,
It contains an acrylic resin having a glass transition temperature (hereinafter referred to as Tg) of 20° C. or lower as a main component.
ここでいうTgが20℃以下のアクリル系樹脂とは、ア
クリル系、メタクリル系の酸及びエステルをはじめとす
るそれらの誘導体等の各種モノマーの単独重合体やそれ
らの共重合体、あるいは例えば他のビニル系モノマーと
の共重合体等のTgが20℃以下のものである。Tgが
20℃以下のアクリル系樹脂としては、例えばポリメチ
ルアクリレート(7g8℃、以下カッコ内に丁gを示す
)、ポリエチルアクリレート(−22℃)、ポリイソプ
ロピルアクリレート(−5℃)、ポリ2−ヒドロキシエ
チルアクリレート(−15℃)、ポリn−ブチルメタク
リレート(20℃)、ポリn−アミルメタクリレート(
10℃)、ポリn−へキシルメタクリレート(−5℃)
、ポリn−オクチルメタクリレート(−20℃)、ポリ
n−テトラドデシルメタクリレート(−9℃)、ポリ2
−エチルヘキシルメタクリレート(−10℃)、ポリ2
−ジメチルアミノエチルメタクリレート(19℃)等が
挙げられるが、これらに限定されるものではない。The acrylic resin with a Tg of 20°C or less herein refers to homopolymers of various monomers such as acrylic and methacrylic acids and esters, and their derivatives, as well as copolymers thereof, or, for example, other polymers. The Tg of a copolymer with a vinyl monomer is 20°C or less. Examples of acrylic resins with a Tg of 20°C or lower include polymethyl acrylate (7g8°C, hereinafter "g" is shown in parentheses), polyethyl acrylate (-22°C), polyisopropyl acrylate (-5°C), poly2 -Hydroxyethyl acrylate (-15°C), poly n-butyl methacrylate (20°C), poly n-amyl methacrylate (
10℃), poly n-hexyl methacrylate (-5℃)
, poly n-octyl methacrylate (-20°C), poly n-tetradodecyl methacrylate (-9°C), poly 2
-Ethylhexyl methacrylate (-10°C), Poly2
-dimethylaminoethyl methacrylate (19°C) and the like, but are not limited to these.
インク受容層用のアクリル系樹脂は上記の如きTgが2
0℃以下の樹脂が用いられ、特に−10℃以下の樹脂が
好適であり、中でも2−エチルヘキシルメタクリレート
樹脂が特に好適である。インク受容層において、該Tg
が20℃以下のアクリル系樹脂は30〜100%含有す
るのが好ましい。The acrylic resin for the ink receiving layer has a Tg of 2 as described above.
A resin having a temperature of 0°C or lower is used, and a resin having a temperature of -10°C or lower is particularly suitable, and 2-ethylhexyl methacrylate resin is particularly suitable. In the ink receiving layer, the Tg
It is preferable that the content of acrylic resin having a temperature of 20° C. or lower is 30 to 100%.
インク受容層の厚さは約2〜10μが好ましく、2μ以
下になると十分なインク定着性が得られず、また10μ
以上としてもそれに見合った効果は得られず製造上、原
材料コスト等において問題を生じてしまう。The thickness of the ink-receiving layer is preferably about 2 to 10 μm; if it is less than 2 μm, sufficient ink fixing properties cannot be obtained;
Even with the above, commensurate effects cannot be obtained, and problems arise in terms of manufacturing, raw material costs, and the like.
本発明の記録シートを構成する表面層は、インク受容層
を保護すると共に記録シートに良好なハンドリング性、
耐ブロッキング性を付与するものであり、かつ記録時に
はワイヤドツトプリンターのヘッド部ワイヤーが表面層
を貫通すべく設けられるものであり、Tgが80℃以上
の樹脂を主成分として含有するものである。The surface layer constituting the recording sheet of the present invention protects the ink-receiving layer and provides the recording sheet with good handling properties.
It imparts blocking resistance, is provided so that the head wire of a wire dot printer penetrates the surface layer during recording, and contains a resin having a Tg of 80° C. or higher as a main component.
表面層用の樹脂としては、アクリル系、メタクリル系の
酸及びエステルをはじめとするそれらの誘導体等の各種
モノマーの単独重合体やそれらの共重合体、あるいは例
えば他のビニル系モノマーとの共重合体等のTgが80
℃以上のものが使用される。Tgが80℃以上の樹脂と
しては、例えばポリアクリル酸(Tg106℃、以下カ
ッコ内にTgを示す〉、ポリメタクリル酸(130℃)
、ポリマレイン酸く130℃)、ポリメチルメタクリレ
ート(105℃)、ポリイソプロピルメタクリレート(
81℃)、ポリt−ブチルメタクリレ−)(107℃)
、ポリフェニルメタクリレート(110℃)、ポリスチ
レン(95℃)、ポリアクリロニトリル(100℃)、
ポリアクリルアミド(153℃)等が挙げられるが、こ
れらに限定されるものではない。Resins for the surface layer include homopolymers and copolymers of various monomers such as acrylic and methacrylic acids and esters, and their derivatives, or copolymers with other vinyl monomers. Tg of merging etc. is 80
℃ or higher is used. Examples of resins with a Tg of 80°C or higher include polyacrylic acid (Tg 106°C, hereinafter Tg is shown in parentheses), polymethacrylic acid (130°C)
, polymaleic acid (130℃), polymethyl methacrylate (105℃), polyisopropyl methacrylate (
81°C), poly t-butyl methacrylate) (107°C)
, polyphenyl methacrylate (110°C), polystyrene (95°C), polyacrylonitrile (100°C),
Examples include, but are not limited to, polyacrylamide (153° C.).
表面層には上記の如きTgが80℃以上の樹脂が用いら
れ、特にメタアクリル系及びスチレン系の樹脂が好まし
く、中でも、メチルメタクリレート、t−ブチルメタク
リレート及びスチレンの各単独重合体またはこれらの共
重合体が特に好適である。表面層において、該Tgが8
0℃以上の樹脂は50〜100%含有するのが好ましい
。For the surface layer, a resin having a Tg of 80° C. or higher as described above is used, and methacrylic and styrene resins are particularly preferred, and among these, methyl methacrylate, t-butyl methacrylate, and styrene homopolymers or copolymers thereof are used. Polymers are particularly preferred. In the surface layer, the Tg is 8
It is preferable that the content of the resin having a temperature of 0° C. or higher is 50 to 100%.
表面層の厚さは約2μ以下が好ましく、2μ以上になる
と良好なインク定若性が得られなくなってしまう。The thickness of the surface layer is preferably about 2 microns or less, and if it is more than 2 microns, good ink stability cannot be obtained.
本発明において支持体としては、例えばポリエチレンテ
レフタレートをはじめとするポリエステル、各種アクリ
ル系及びメタクリル系ポリマー、ポリ塩化ビニル、ポリ
カーボネート、ポリイミド、アセテート、セロハン、セ
ルロイド等のプラスチックフィルム又はシート、更に合
成繊維シート、金属蒸着フィルム等が挙げられるが、こ
れらに限定されるものではなく、記録目的や用途に応じ
て表面に設けるインク受容層の密着性を考慮して適宜選
択すればよい。In the present invention, the support includes, for example, polyester such as polyethylene terephthalate, various acrylic and methacrylic polymers, plastic films or sheets such as polyvinyl chloride, polycarbonate, polyimide, acetate, cellophane, and celluloid, as well as synthetic fiber sheets, Examples include metal-deposited films, but the film is not limited to these, and may be selected as appropriate in consideration of the adhesion of the ink-receiving layer provided on the surface depending on the recording purpose and use.
本発明の記録シートは以上の如き、支持体、インク受容
層及び表面層よりなるものであるが、これらには必要に
応じて各種添加剤を添加することができる。例えばハン
ドリング性向上、ブロッキング性向上等の目的でポリエ
チレンオキサイド、シリカ、クレー、タルク、カオリン
、ケイソウ土、炭酸カルシウム、硫酸カルシウム、硫酸
バリウム、ケイ酸アルミニウム、合成ゼオライト、アル
ミナ、酸化亜鉛、リトポン、サテンホワイト等の顔料を
添加したり、更にシートの生産性、記録特性等を高める
目的で、分散剤、蛍光染料、消泡剤、潤滑剤、低抵抗剤
等の添加剤も使用することができる。The recording sheet of the present invention is composed of the support, the ink receiving layer and the surface layer as described above, and various additives may be added to these as necessary. For example, polyethylene oxide, silica, clay, talc, kaolin, diatomaceous earth, calcium carbonate, calcium sulfate, barium sulfate, aluminum silicate, synthetic zeolite, alumina, zinc oxide, lithopone, satin, etc. are used to improve handling and blocking properties. In addition to adding pigments such as white, additives such as dispersants, fluorescent dyes, antifoaming agents, lubricants, and low-resistance agents can also be used for the purpose of improving sheet productivity, recording characteristics, and the like.
本発明の記録シートを製造するには、各層を形成するた
めの材料を水または適当な溶剤中に溶解または分散させ
て調製した塗工液を、ロールコーティング法、プレート
コーティング法、スプレーコーティング法、エアナイフ
コーティング法、ロッドバーコーティング法等の方法に
よって塗布・乾燥する方法、また前記の各層を形成する
ための材料を均一に混合した混合物をホットメルトコー
ティング法、ラミネートコーティング法等によって積層
する方法等があり、使用する材料に応じてこれらの方法
を適宜選択して、支持体上にインク受容層、表面層を順
次積層してやればよい。In order to produce the recording sheet of the present invention, a coating solution prepared by dissolving or dispersing the materials for forming each layer in water or an appropriate solvent is applied using a roll coating method, a plate coating method, a spray coating method, or the like. There are methods such as applying and drying by air knife coating method, rod bar coating method, etc., and methods of laminating a mixture of uniformly mixed materials for forming each layer by hot melt coating method, laminate coating method, etc. The ink-receiving layer and the surface layer may be sequentially laminated on the support by appropriately selecting one of these methods depending on the material used.
なお、本発明の記録シートにおいて、支持体の裏面、す
なわちインク受容層と表面層が形成されていない面上に
、一般に使用されている粘着剤を用いて粘着層を設け、
更に必要に応じて離型性を有する離型フィルム又はシー
トを粘着層に積層してやることによって、任意に貼着す
ることの可能な粘着シート又はラベルとして使用するこ
ともでき、本発明の記録シートの使用領域を太き(広げ
ることができる。In the recording sheet of the present invention, an adhesive layer is provided on the back side of the support, that is, on the side where the ink receiving layer and the surface layer are not formed, using a commonly used adhesive,
Furthermore, if necessary, by laminating a release film or sheet with release properties on the adhesive layer, it can be used as an adhesive sheet or label that can be attached as desired. The usage area can be thickened (widened).
本発明におけるガラス転移温度の測定法は、下記の通り
である。補償方式の示差走査熱量計を用いて、標準物質
としてアルミナを使用して測定を行い、第1図に示す如
(吸熱曲線1においてベースライン3と吸熱ピークとの
それぞれの線の延長線上の交点2の温度をガラス転移温
度とした。The method for measuring the glass transition temperature in the present invention is as follows. Measurements were performed using a differential scanning calorimeter with a compensation method and alumina as a standard substance, as shown in Fig. The temperature of No. 2 was taken as the glass transition temperature.
〈実施例〉
次に実施例に従って本発明を説明する。なお、配合を表
す部数は全て重量部を示す。<Examples> Next, the present invention will be explained according to examples. In addition, all parts expressing the formulation indicate parts by weight.
実施例1
厚さ100μのポリエチレンテレフタレートフフィルム
の片面に、下記組成よりなる塗液をメーヤバーコーター
で塗布・乾燥してインク受容層を形成した。なお、イン
ク受容層の膜厚は5μとした。Example 1 A coating liquid having the following composition was coated on one side of a polyethylene terephthalate film having a thickness of 100 μm using a Meyer bar coater and dried to form an ink-receiving layer. Note that the thickness of the ink receiving layer was 5 μm.
次にインク受容層の表面に、下記組成よりなる塗液をグ
ラビアコーターで塗布・乾燥して表面層を形成して本発
明の記録シートを作製した。なお、表面層の膜厚は1μ
とした。Next, a coating liquid having the following composition was applied to the surface of the ink-receiving layer using a gravure coater and dried to form a surface layer, thereby producing a recording sheet of the present invention. The thickness of the surface layer is 1μ.
And so.
実施例2
表面層用塗液として下記組成のものを使用した以外は実
施例1と全(同様にして本発明の記録シートを得た。Example 2 A recording sheet of the present invention was obtained in the same manner as in Example 1 except that the coating liquid for the surface layer had the following composition.
実施例3
表面層用塗液として下記組成のものを使用した以外は実
施例1と全く同様にして本発明の記録シートを得た。Example 3 A recording sheet of the present invention was obtained in exactly the same manner as in Example 1, except that the coating liquid for the surface layer had the following composition.
実施例4
インク受容層用塗液として下記組成のものを使用した以
外は実施例1と全く同様にして本発明の記録シートを得
た。Example 4 A recording sheet of the present invention was obtained in exactly the same manner as in Example 1, except that the coating liquid for the ink-receiving layer had the following composition.
実施例5
支持体として厚さ125μの乳白ポリエチレンテレフタ
レートフィルムを使用した以外は実施例1と全(同様に
して本発明の記録シートを得た。Example 5 A recording sheet of the present invention was obtained in the same manner as in Example 1 except that a 125 μm thick opalescent polyethylene terephthalate film was used as the support.
実施例6
支持体として厚さ100μの二軸延伸ポリプロピレンフ
ィルムを使用した以外は実施例1と全(同様にして本発
明の記録シートを得た。Example 6 A recording sheet of the present invention was obtained in the same manner as in Example 1 except that a biaxially stretched polypropylene film having a thickness of 100 μm was used as the support.
比較例1
インク受容層用塗液として下記組成のものを使用した以
外は実施例1と全く同様にして比較用の記録シートを作
製した。Comparative Example 1 A comparative recording sheet was prepared in exactly the same manner as in Example 1, except that the coating liquid for the ink-receiving layer had the following composition.
比較例2
表面層用塗液として下記組成のものを使用した以外は実
施例1と全く同様にして比較用の記録シートを作製した
。Comparative Example 2 A comparative recording sheet was prepared in exactly the same manner as in Example 1, except that the coating liquid for the surface layer had the following composition.
比較例3
厚さ100μのポリエチレンテレフタレートフィルムに
下記組成よりなる塗液をメーヤバーコーターで膜厚5μ
となるように塗布・乾燥して比較用の記録シートを作製
した。Comparative Example 3 A coating liquid having the following composition was coated on a polyethylene terephthalate film with a thickness of 100μ using a Meyer bar coater to a film thickness of 5μ.
A recording sheet for comparison was prepared by coating and drying to give the following properties.
上記実施例1〜6及び比較例1〜3で得られた記録シー
トについて、ワイヤドツトプリンター(NEC社製、P
C−PR201、インクリボンはPC−PR−201−
01を使用)を用いて印字試験をした。その結果は表−
1に示す通りであり、本発明の記録シートはワックス系
物質を基材とするインクリボンで印字するワイヤドツト
プリンターでの使用において、極めて良好なインク保持
能力を発揮することが確認された。Regarding the recording sheets obtained in Examples 1 to 6 and Comparative Examples 1 to 3, wire dot printers (manufactured by NEC Corporation, P
C-PR201, ink ribbon is PC-PR-201-
A printing test was conducted using 01). The results are shown in the table-
1, it was confirmed that the recording sheet of the present invention exhibits extremely good ink retention ability when used in a wire dot printer that prints with an ink ribbon based on a wax-based substance.
表−1
なお、表−1における各項目の評価方法は以下の通りで
ある。Table-1 The evaluation method for each item in Table-1 is as follows.
(1)インク着肉性:目視判定で良好なものを○、不良
なものを×とした。(1) Ink receptivity: Visually evaluated good results as ◯, and poor results as ×.
(:2)インク保持性:印字直後に印字部を指先でこす
り、インクが落ちず良好なもの
を○、インクが落ちてしまうも
のを×とした。(:2) Ink retention: Immediately after printing, the printed area was rubbed with a fingertip. If the ink did not come off, it was evaluated as ○, and if the ink did come off, it was evaluated as bad.
〈発明の効果〉
本発明の記録シートは勝れたインク保持能力を有するた
め、従来ワイヤドツトプリンターによる印字が実用上不
可能であったプラスチックフィルム等の紙以外のシート
状物への印字を可能ならしめるものであり、クリーンル
ーム内での使用や、オーバーヘッドプロジェクタ−用シ
ートへの印字、その他さまざまな非常に広範囲の用途に
ワイヤドツトプリンターを使用することができるという
利点を有するものである。<Effects of the Invention> Since the recording sheet of the present invention has excellent ink retention ability, it is possible to print on sheet-like materials other than paper such as plastic films, which were practically impossible to print with conventional wire dot printers. This has the advantage that the wire dot printer can be used in a very wide range of applications, including use in clean rooms, printing on sheets for overhead projectors, and many other applications.
第1図は本発明におけるガラス転移温度の求め方を示す
図である。
1・・・吸熱曲線 2・・・交点3・・・ベー
スラインFIG. 1 is a diagram showing how to determine the glass transition temperature in the present invention. 1... Endothermic curve 2... Intersection point 3... Baseline
Claims (3)
20℃以下のアクリル系樹脂を主成分とするインク受容
層、及びガラス転移温度が80℃以上の樹脂を主成分と
する表面層を順次積層したことを特徴とする記録シート
。(1) On at least one side of the support, an ink-receiving layer mainly composed of an acrylic resin with a glass transition temperature of 20°C or lower and a surface layer mainly composed of a resin with a glass transition temperature of 80°C or higher are sequentially formed. A recording sheet characterized by being laminated.
2−エチルヘキシルメタクリレート樹脂であることを特
徴とする特許請求の範囲第1項記載の記録シート。(2) The recording sheet according to claim 1, wherein the acrylic resin having a glass transition temperature of 20° C. or lower is 2-ethylhexyl methacrylate resin.
クリレート、t−ブチルメタクリレート及びスチレンの
各単独重合体及びこれらの共重合体の中より選ばれた少
なくとも1種の重合体であることを特徴とする特許請求
の範囲第1項記載の記録シート。(3) The resin having a glass transition temperature of 80°C or higher is at least one polymer selected from methyl methacrylate, t-butyl methacrylate, styrene homopolymers, and copolymers thereof. A recording sheet according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63110466A JPH01282399A (en) | 1988-05-09 | 1988-05-09 | Recording sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63110466A JPH01282399A (en) | 1988-05-09 | 1988-05-09 | Recording sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01282399A true JPH01282399A (en) | 1989-11-14 |
Family
ID=14536421
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63110466A Pending JPH01282399A (en) | 1988-05-09 | 1988-05-09 | Recording sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01282399A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5668188A (en) * | 1979-11-06 | 1981-06-08 | Mitsubishi Paper Mills Ltd | Production of coated paper for printing |
JPS5713679A (en) * | 1980-06-06 | 1982-01-23 | Elpag Ag Chur | Heat exchange element |
JPS6375199A (en) * | 1986-09-10 | 1988-04-05 | 新王子製紙株式会社 | Release paper |
-
1988
- 1988-05-09 JP JP63110466A patent/JPH01282399A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5668188A (en) * | 1979-11-06 | 1981-06-08 | Mitsubishi Paper Mills Ltd | Production of coated paper for printing |
JPS5713679A (en) * | 1980-06-06 | 1982-01-23 | Elpag Ag Chur | Heat exchange element |
JPS6375199A (en) * | 1986-09-10 | 1988-04-05 | 新王子製紙株式会社 | Release paper |
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