JPH04288288A - Base paper for thermal screen printing - Google Patents
Base paper for thermal screen printingInfo
- Publication number
- JPH04288288A JPH04288288A JP5230591A JP5230591A JPH04288288A JP H04288288 A JPH04288288 A JP H04288288A JP 5230591 A JP5230591 A JP 5230591A JP 5230591 A JP5230591 A JP 5230591A JP H04288288 A JPH04288288 A JP H04288288A
- Authority
- JP
- Japan
- Prior art keywords
- film
- base paper
- support
- fine particles
- particles
- 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.)
- Withdrawn
Links
- 238000007650 screen-printing Methods 0.000 title abstract 3
- 239000010419 fine particle Substances 0.000 claims abstract description 29
- 238000007639 printing Methods 0.000 claims abstract description 17
- 239000012790 adhesive layer Substances 0.000 claims description 3
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 239000004416 thermosoftening plastic Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 abstract description 32
- 239000007787 solid Substances 0.000 abstract description 8
- 239000000853 adhesive Substances 0.000 description 24
- 230000001070 adhesive effect Effects 0.000 description 24
- 239000000835 fiber Substances 0.000 description 23
- 238000000034 method Methods 0.000 description 17
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- -1 polypropylene Polymers 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 230000007423 decrease Effects 0.000 description 10
- 241000519995 Stachys sylvatica Species 0.000 description 7
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000011148 porous material Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 150000002009 diols Chemical class 0.000 description 5
- 229920001225 polyester resin Polymers 0.000 description 5
- 239000004645 polyester resin Substances 0.000 description 5
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001723 curing Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 238000001227 electron beam curing Methods 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 239000010954 inorganic particle Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000003094 microcapsule Substances 0.000 description 2
- 239000011146 organic particle Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 1
- 244000198134 Agave sisalana Species 0.000 description 1
- 235000011624 Agave sisalana Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920001634 Copolyester Polymers 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
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 240000000907 Musa textilis Species 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000010191 image analysis Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000779 poly(divinylbenzene) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Printing Plates And Materials Therefor (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、感熱孔版印刷分野で使
用される、熱可塑性樹脂延伸フイルム(以下、フイルム
と略す)とインク透過性多孔質支持体(以下、支持体と
略す)とを貼り合わせてなる感熱孔版印刷用原紙(以下
、原紙と略す)であり、特に、孔版印刷特有の支持体繊
維に由来する白抜けを著しく減少させることにより、印
刷画像性を向上させることを目的とした原紙に関するも
のである。[Industrial Application Field] The present invention relates to a stretched thermoplastic resin film (hereinafter referred to as a film) and an ink permeable porous support (hereinafter referred to as a support) used in the field of thermal stencil printing. It is a base paper for heat-sensitive stencil printing (hereinafter referred to as base paper) that is laminated together, and its purpose is to improve printing image quality by significantly reducing white spots originating from the support fibers that are unique to stencil printing. This relates to the original paper.
【0002】0002
【従来の技術】一般に、感熱孔版印刷では、原稿の文字
、図形に対応して、サーマルヘッド等の熱源を用いて熱
的に原紙のフイルムを溶融穿孔し、フイルムに孔を形成
した後、原紙の支持体側からインクを供給し、孔部分か
らインクを滲出させることで印刷を行っている。[Prior Art] In general, in thermal stencil printing, a heat source such as a thermal head is used to thermally melt and perforate a base paper film in accordance with the characters and figures on the original, and after forming holes in the film, the base paper is Printing is performed by supplying ink from the support side and allowing the ink to seep out from the holes.
【0003】従来より、感熱孔版印刷では、熱可塑性樹
脂延伸フイルム、例えばポリエステル系、塩化ビニリデ
ン系、塩化ビニル系、ポリプロピレン系等のフイルムと
、天然繊維や合成繊維等からなる不織布(薄葉紙)、織
布(紗)等の支持体を接着剤で貼り合わせた原紙が用い
られている。(例えば、特開昭51−2513号公報、
特開昭57−182495号公報、特公昭49−593
3号公報)近年、孔版印刷分野でその解像度を向上させ
る手段のひとつとして、製版用サーマルヘッドの熱素子
の高密度化が検討され、その素子サイズが非常に小さい
もの(400ドット/インチのもので素子間ピッチが6
3.5μm)が全自動孔版印刷機に搭載されるようにな
ってきた。Conventionally, heat-sensitive stencil printing uses stretched thermoplastic resin films such as polyester-based, vinylidene chloride-based, vinyl chloride-based, and polypropylene-based films, and nonwoven fabrics (thin paper) and woven fabrics made of natural fibers, synthetic fibers, etc. Base paper is used, which is made by bonding a support such as cloth (gauze) with an adhesive. (For example, Japanese Patent Application Laid-Open No. 51-2513,
Japanese Unexamined Patent Publication No. 57-182495, Japanese Patent Publication No. 49-593
(No. 3 Publication) In recent years, as a means of improving the resolution in the stencil printing field, increasing the density of thermal elements in plate-making thermal heads has been studied, and The pitch between the elements is 6.
3.5 μm) is now being installed in fully automatic stencil printing machines.
【0004】0004
【発明が解決しようとする課題】そこで、本発明者は、
素子高密度化を直接的に画像性向上に反映させることを
目的として、サーマルヘッドの素子密度に対応した孔を
、フイルム上に独立に形成するための検討を行ってきた
(特願平2−149924号公報)。それらの検討を進
める中で、サーマルヘッドの素子サイズのみを単に小さ
くしても、著しい画像性の向上には結びつかず、用いる
原紙の構造、つまりフイルムと支持体との接着部分の影
響を考慮した原紙を開発しなければならないことを見い
出した。[Problem to be solved by the invention] Therefore, the inventors of the present invention
With the aim of directly reflecting the increase in element density in improving image quality, we have been studying how to independently form holes on the film that correspond to the element density of the thermal head (Patent Application No. 149924). As we proceeded with these studies, we found that simply reducing the element size of the thermal head did not lead to significant improvements in image quality, and we considered the structure of the base paper used, that is, the influence of the adhesive part between the film and the support. I discovered that I had to develop a base paper.
【0005】つまり、従来の原紙では、フイルムと支持
体表面の繊維が接着されているため、その接着部分の形
状は、ほぼ繊維の径に近い幅で線状にならざるをえず、
しかも、一般に支持体として使われている薄葉紙では、
繊維の結束(繊維が数本凝集している部分)は避けられ
ないため、その部分での接着形状は、数本の繊維が並ん
だ帯状になっている。このような接着形状の原紙では、
製版してもその接着部分は部分的にしか開孔せずフイル
ムがそのまま残存し、印刷したとしても、その部分には
インクが回り込まず白い部分として残ることになる。い
わゆる孔版印刷での白抜けといわれる現象であり、従来
の原紙では繊維状の白抜けは避けられないものとされて
いる。In other words, in conventional base paper, since the film and the fibers on the surface of the support are bonded, the shape of the bonded portion has to be linear with a width approximately close to the diameter of the fibers.
Moreover, the thin paper that is generally used as a support,
Since binding of fibers (areas where several fibers are aggregated) is unavoidable, the adhesive shape at that area is a band-like shape in which several fibers are lined up. For base paper with such adhesive shape,
Even if the plate is made, the adhesive part will only be partially opened and the film will remain intact, and even if it is printed, the ink will not get around to that part and it will remain as a white part. This is a phenomenon called white spots in stencil printing, and fibrous white spots are unavoidable in conventional base paper.
【0006】加えて、サーマルヘッドの素子サイズが小
さくなる程、製版に及ぼす支持体繊維とフイルムとの接
着部分の影響が強くなり、本来開孔すべきところが開孔
しないドットの個数が増えていくことになる。In addition, as the element size of the thermal head becomes smaller, the influence of the bond between the support fiber and the film on plate making becomes stronger, and the number of dots that do not open where they should originally open increases. It turns out.
【0007】[0007]
【問題点を解決するための手段】本発明者は、原紙のフ
イルムと支持体の接着形状について鋭意研究を重ねた結
果、接着形状を点状に分散させることで、従来の原紙と
比べ著しく画像性の向上した原紙を開発するに至った。
すなわち、本発明は熱可塑性フイルムとインク透過性多
孔質支持体を貼り合せてなる感熱孔版印刷用原紙におい
て、接着層に50μm以下の微粒子が存在することを特
徴とする感熱孔版印刷用原紙である。[Means for Solving the Problems] As a result of extensive research into the adhesive shape between the base paper film and the support, the present inventor has discovered that by dispersing the adhesive shape in dots, the image is significantly improved compared to conventional base paper. This led to the development of a base paper with improved properties. That is, the present invention is a base paper for heat-sensitive stencil printing made by laminating a thermoplastic film and an ink-permeable porous support, characterized in that fine particles of 50 μm or less are present in the adhesive layer. .
【0008】本発明の最も重要なことは、従来の原紙が
、フイルムと支持体繊維の接触部分で、フイルムと支持
体とが接着されていたのに比べ、本発明の原紙は、フイ
ルムと支持体とが主に微粒子を介して接着されているこ
とにある。つまり、本発明の原紙では、フイルムの接着
固定された部分がより小さい面積となるため、フイルム
が熱製版されるときにフイルムの穿孔を接着部分が阻害
する影響が、従来の原紙に比べ著しく少なくなるため、
フイルムの開孔状態が均一なものとなる。しかも、従来
の原紙では避けられなかった、支持体繊維の結束部での
フイルム穿孔阻害とインク透過阻害に由来する、印刷物
の黒ベタ部での白抜けが、本発明の原紙では主に微粒子
を介しての接着のため、著しく減少することになる。The most important aspect of the present invention is that in contrast to the conventional base paper in which the film and the support were bonded at the contact area between the film and the support fibers, the base paper of the present invention has a bond between the film and the support fiber. The main reason for this is that it is attached to the body mainly through fine particles. In other words, in the base paper of the present invention, since the area where the film is adhesively fixed is smaller, the influence of the adhesive part on the perforation of the film when the film is thermally plated is significantly less than that of conventional base paper. To become
The opening state of the film becomes uniform. Moreover, the white spots in the black solid areas of printed materials, which were unavoidable with conventional base paper due to the inhibition of film perforation and ink permeation at the binding part of the support fibers, are mainly caused by fine particles in the base paper of the present invention. This will be significantly reduced due to the adhesion through.
【0009】接着層に50μm以下の微粒子を存在させ
る方法としては、具体的には、接着剤に微粒子を存在さ
せるか、支持体あるいはフイルムにあらかじめ微粒子を
固着させるか、またはこれらの組合せにより接着層に微
粒子を存在させることが出来る。支持体とフイルムの接
着部に効率よく微粒子を存在させるにはフイルムあるい
は支持体にあらかじめ固着させることであり、より効率
のよいのは支持体に微粒子を固着させることである。[0009] Specifically, the method of making fine particles of 50 μm or less exist in the adhesive layer is to make the fine particles exist in the adhesive, to fix the fine particles to a support or film in advance, or by a combination of these methods. fine particles can be present in the In order to efficiently make the fine particles exist at the adhesive portion between the support and the film, it is necessary to make them adhere to the film or the support in advance, and it is more efficient to make the fine particles adhere to the support.
【0010】本発明で用いる微粒子とは、完全に真球で
ある必要はなく、ある程度の形状の分布をもちながら平
均的にみれば球形状のものであれば良い。ここでの微粒
子はその粒径つまり直径が、最大50μm以下である必
要がある。粒径が50μmを越えるものは、原紙として
の厚みが厚くなりすぎるため、また、フイルムとの接着
部分の面積が広くなりすぎるため本発明には適さない。
粒径の下限は用いる支持体の繊維間隔部分を著しく埋め
、インクの透過性を阻害しなければ良く、この下限は支
持体繊維の分散状態で適宜決めれば良い。最大粒径の好
ましい範囲としては、40μm以下、より好ましくは3
0μm以下、さらに好ましくは20μm以下である。
また、粒径分布としては、分布幅の小さいものほど好ま
しいが特に限定はせず用いることができる。また、平均
粒径としては、数平均粒径として5〜40μm、好まし
くは10〜30μm、特に好ましくは15〜20μmで
ある。ここでいう粒径及び平均粒径は、粒子を拡大し画
像解析装置(例えば、日本アビオニクス(株)製、SP
ICCA−II) にて測定した値を用いる。[0010] The fine particles used in the present invention do not need to be completely spherical, but may have a spherical shape on average while having a certain degree of shape distribution. The fine particles here need to have a particle size, that is, a diameter of 50 μm or less at maximum. Particles with a particle size exceeding 50 μm are not suitable for the present invention because the thickness as a base paper becomes too thick and the area of the adhesive portion with the film becomes too large. The lower limit of the particle size may be determined as long as it does not significantly fill the space between the fibers of the support used and inhibit ink permeability, and this lower limit may be determined as appropriate depending on the dispersion state of the support fibers. The preferred range of maximum particle size is 40 μm or less, more preferably 3 μm or less.
It is 0 μm or less, more preferably 20 μm or less. Further, as for the particle size distribution, the smaller the distribution width is, the more preferable it is, but it can be used without any particular limitation. Moreover, the average particle size is 5 to 40 μm, preferably 10 to 30 μm, and particularly preferably 15 to 20 μm as a number average particle size. The particle size and average particle size here are determined by enlarging the particles and using an image analysis device (for example, Nippon Avionics Co., Ltd., SP
The value measured by ICCA-II) is used.
【0011】また、ここでの微粒子とは、熱可塑性樹脂
、熱硬化性樹脂等の有機系粒子や、無機系粒子いずれで
も良く、その構造も均一固体のもの、また、いわゆるマ
イクロカプセルと称される中空状のものいずれでも良い
。たとえば、有機系粒子としては、ポリスチレン、ポリ
ジビニルベンゼン、ポリメチルメタクリレート、ポリア
ミド、ポリエステル、ポリエチレン、ポリプロピレン、
ポリ酢酸ビニル、ポリアクニロリトリル、ポリ塩化ビニ
ル、ポリ塩化ビニリデン、エチルセルロース、ニトロセ
ルロース、ポリテトラフルオロエチレン、ポリビニリデ
ンフルオライド、有機シリコン等、および、これらの共
重合樹脂、また、無機粒子としては、酸化ケイ素、酸化
アルミ、酸化チタン、カーボンブラック等の微粒子が好
適に用いられる。その中でも、サーマルヘッドの摩耗劣
化および腐食劣化を考慮した場合、ハイドロカーボン系
の有機合成樹脂の微粒子が特に好適に用いられる。
さらに、マイクロカプセル状の気体を含有する中空体粒
子は、その断熱性能により熱効率良く製版されると考え
られる。[0011] The fine particles herein may be either organic particles such as thermoplastic resins or thermosetting resins, or inorganic particles, and may have a uniform solid structure, or may be so-called microcapsules. Any hollow shape may be used. For example, organic particles include polystyrene, polydivinylbenzene, polymethyl methacrylate, polyamide, polyester, polyethylene, polypropylene,
Polyvinyl acetate, polyacnylotrile, polyvinyl chloride, polyvinylidene chloride, ethyl cellulose, nitrocellulose, polytetrafluoroethylene, polyvinylidene fluoride, organic silicone, etc., and their copolymer resins, as well as inorganic particles. , silicon oxide, aluminum oxide, titanium oxide, carbon black, and the like are preferably used. Among these, in consideration of abrasion deterioration and corrosion deterioration of the thermal head, fine particles of hydrocarbon-based organic synthetic resin are particularly preferably used. Furthermore, it is believed that hollow particles containing gas in the form of microcapsules can be made into plates with good thermal efficiency due to their heat insulating properties.
【0012】フイルムおよび/または支持体に固着した
微粒子を主な接着点として、フイルムと支持体とを接着
させるためには、いくつかの方法が考えられるが、適宜
選択されうる。例えば、粒子を分散させた固剤溶液を、
塗工装置にて支持体表面に塗布し、その後溶剤を飛散さ
せ、表面に粒子の固着した支持体を製造した後フイルム
とラミネートする方法、また、粒子を分散させた固着剤
溶液を、塗工装置にてフイルム表面に塗布し、その後溶
剤を飛散させ、表面に粒子の固着したフイルムを製造し
た後支持体とラミネートする方法、さらには、フイルム
と支持体に各々粒子を固着させた後に、固着面を接着面
としてラミネートする方法等がある。また、粒子を固着
させるための固着剤を接着剤として兼用し、粒子固着と
同時にラミネートも行う方法等も取りうる。また、支持
体である薄葉紙製造時に支持体表面に粒子を固着できれ
ばそれでも良い。またさらには、最終的なフイルム厚み
より粒径の大きい微粒子を、原反フイルムに分散させた
状態で成形し得られた、粒径の突起を形成したフイルム
を、粒子の固着したフイルムとして用いることも可能で
ある。Several methods can be considered for bonding the film and the support using the fine particles fixed to the film and/or the support as the main bonding points, and any method can be selected as appropriate. For example, a solid solution with particles dispersed in it,
A method of coating the surface of a support with a coating device, then scattering a solvent to produce a support with particles fixed to the surface, and then laminating it with a film, or coating a fixing agent solution with particles dispersed There is a method in which the film is coated on the surface of the film using a device, and then a solvent is scattered to produce a film with particles fixed to the surface, which is then laminated with a support. There are methods such as laminating with the surface as an adhesive surface. It is also possible to adopt a method in which a fixing agent for fixing the particles is also used as an adhesive, and lamination is performed at the same time as fixing the particles. Furthermore, it is acceptable if the particles can be fixed to the surface of the support during production of the thin paper that is the support. Furthermore, a film with protrusions of a particle size formed by molding fine particles having a particle size larger than the final film thickness in a state where they are dispersed in a raw film can be used as a film to which particles are fixed. is also possible.
【0013】ここでの固着剤としては、通常公知の溶剤
型、ホットメルト型、エマルジョン・ラテックス型、反
応硬化型、紫外線および電子線硬化型等の各種接着剤が
、フイルムの穿孔適性、インキの透過性を妨げない条件
で使用され、その量は、0.5〜5g/m2 、好まし
くは0.5〜3g/m2、より好ましくは0.5〜2g
/m2 である。いずれの方法においても、粒子の凝集
を防止するために各種の分散剤を接着強度を低下させな
い程度に添加したり、また、支持体の表面に有効に粒子
を存在させるため、加工時にエアノズルやサクション等
を有効に用いても良い。[0013] As the fixing agent here, various types of adhesives such as commonly known solvent type, hot melt type, emulsion latex type, reaction curing type, ultraviolet ray and electron beam curing type etc. It is used under conditions that do not impede permeability, and its amount is 0.5 to 5 g/m2, preferably 0.5 to 3 g/m2, more preferably 0.5 to 2 g.
/m2. In either method, to prevent particle agglomeration, various dispersants are added to an extent that does not reduce adhesive strength, and air nozzles or suctions are used during processing to effectively make particles exist on the surface of the support. etc. may be used effectively.
【0014】ここでは、完全に微粒子のみを介してのフ
イルムと支持体との接着が理想的であるが、フイルムと
支持体繊維部分での接着が著しく画像性を低下させない
範囲で存在しても良く、主として微粒子を介して接着さ
れていれば良い。微粒子の固着分布密度は、用いる微粒
子の粒径及び支持体の密度、坪量により、その最適域は
変わるが、通常2〜60個/mm2 であり、好ましく
は3〜40個/mm2 、さらに好ましくは4〜30個
/mm2 である。[0014] Here, it is ideal that the film and the support be completely bonded only through the fine particles, but even if the adhesion between the film and the support fibers does not significantly deteriorate the image quality. It is sufficient if the bonding is mainly through fine particles. The optimal range of the fixed distribution density of fine particles varies depending on the particle size of the fine particles used and the density and basis weight of the support, but it is usually 2 to 60 particles/mm2, preferably 3 to 40 particles/mm2, and more preferably is 4 to 30 pieces/mm2.
【0015】フイルムと支持体を微粒子を介して貼り合
わせるための接着剤としては、通常公知の溶剤型、ホッ
トメルト型、エマルジョン・ラテックス型、反応硬化型
、紫外線および電子線硬化型等の各種接着剤が、フイル
ムの穿孔適性、インキの透過性を妨げない条件で使用さ
れうる。さらに、接着剤の塗布は通常公知の方法で実施
され、フイルム側、支持体側または両者に接着剤を塗布
して貼り合わせればよい。接着剤の量としては、0.1
〜5g/m2 、好ましくは0.5〜3g/m2 、よ
り好ましくは0.5〜2g/m2 である。[0015] As the adhesive for bonding the film and the support through fine particles, there are various types of adhesives known in the art, such as solvent type, hot melt type, emulsion latex type, reaction curing type, ultraviolet ray and electron beam curing type, etc. The agent can be used under conditions that do not interfere with the perforability of the film and the permeability of the ink. Further, the application of the adhesive is usually carried out by a known method, and the adhesive may be applied to the film side, the support side, or both, and then the films are bonded together. The amount of adhesive is 0.1
-5 g/m2, preferably 0.5-3 g/m2, more preferably 0.5-2 g/m2.
【0016】本発明の原紙に用いるフイルムとしては、
加熱収縮率が少なくとも30%、加熱収縮応力値が少な
くとも75g/mm2 の特性を有する、厚さ0.5〜
4μmの熱可塑性樹脂フイルムが用いられる。まず、フ
イルムの加熱収縮率は30%以上であることが必要であ
り、好ましくは30〜90%、より好ましくは40〜8
0%の範囲である。なお、この加熱収縮率は、50mm
角のフイルムをサンプリングし、測定温度に設定した恒
温槽に入れ、自由に収縮する状態で10分間処理した後
、フイルムの収縮量を求め、元の寸法に対する百分率で
表した。この加熱収縮率は、好ましくは測定温度が60
〜170℃、より好ましくは65〜140℃の範囲にお
いて発現することが望ましい。この加熱収縮率が30%
未満の場合、穿孔時の開孔が不十分となり、また、90
%を越える場合、孔が拡大したり寸法安定性が低下する
傾向にあり好ましくない。また、この加熱収縮率が60
℃未満で発現する場合、フイルムの寸法安定性の低下や
孔が拡大することによる解像度の低下する傾向にあり、
170℃を越えて発現する場合、穿孔感度が低下する傾
向にあり好ましくない。The film used for the base paper of the present invention is as follows:
Thickness of 0.5 to 100 mm, with a heat shrinkage rate of at least 30% and a heat shrinkage stress value of at least 75 g/mm2.
A 4 μm thermoplastic resin film is used. First, the heat shrinkage rate of the film needs to be 30% or more, preferably 30 to 90%, more preferably 40 to 8%.
The range is 0%. In addition, this heat shrinkage rate is 50mm
A corner film was sampled, placed in a constant temperature bath set to the measurement temperature, and allowed to shrink freely for 10 minutes.The amount of shrinkage of the film was determined and expressed as a percentage of the original size. This heat shrinkage rate is preferably measured at a temperature of 60
It is desirable that the temperature is expressed in the range of 170°C to 170°C, more preferably 65 to 140°C. This heating shrinkage rate is 30%
If it is less than 90, the opening during drilling will be insufficient, and
If it exceeds %, the pores tend to enlarge and the dimensional stability tends to decrease, which is not preferable. In addition, this heat shrinkage rate is 60
If it occurs at temperatures below ℃, the dimensional stability of the film tends to decrease and the resolution tends to decrease due to enlarged pores.
When the temperature exceeds 170°C, the perforation sensitivity tends to decrease, which is not preferable.
【0017】さらに、このフイルムは、少なくとも75
g/mm2 以上、好ましくは100〜1200g/m
m2 、さらに好ましくは150〜1000g/mm2
の加熱収縮応力値をもつことが必要である。この加熱
収縮応力値は該層フイルムを10mm幅の短冊状にサン
プリングし、これをストレンゲージ付きのチャックに、
チャック間を50mmにしてセットし、これを各設定温
度に加熱したシリコンオイル中に浸漬し、発生する応力
を測定した。設定温度が100℃以下では、浸漬してか
ら10秒後の値、100℃を越える場合は5秒後の値を
求め、縦、横方向の平均値を採用した。さらに、この加
熱収縮応力値は、60〜150℃、好ましくは60〜1
40℃、より好ましくは70〜130℃の範囲において
発現することが望ましい。この加熱収縮応力値の75g
/mm2 未満のものは、穿孔時の開孔が不十分であり
、また1200g/mm2 を越えると孔が広がりすぎ
たり、フイルムが歪んだりして解像度が低下する傾向に
ある。また、この加熱収縮応力値が60℃未満で発現す
る場合、フイルムの寸法安定性の低下や孔が拡大するこ
とによる解像度の低下する傾向にあり、150℃を越え
て発現する場合、穿孔感度が低下する傾向にあり好まし
くない。Furthermore, this film has at least 75
g/mm2 or more, preferably 100 to 1200 g/m
m2, more preferably 150 to 1000 g/mm2
It is necessary to have a heat shrinkage stress value of . This heat shrinkage stress value is obtained by sampling the layered film into a strip shape with a width of 10 mm, and placing it in a chuck with a strain gauge.
The chucks were set with a gap of 50 mm and immersed in silicone oil heated to each set temperature, and the stress generated was measured. When the set temperature was 100°C or less, the value was determined 10 seconds after immersion, and when it exceeded 100°C, the value was determined after 5 seconds, and the average value in the vertical and horizontal directions was adopted. Furthermore, this heat shrinkage stress value is 60 to 150°C, preferably 60 to 1
It is desirable that the temperature is expressed at 40°C, more preferably in the range of 70 to 130°C. 75g of this heat shrinkage stress value
If the diameter is less than 1200 g/mm2, the openings during drilling will be insufficient, and if it exceeds 1200 g/mm2, the pores will become too wide and the film will become distorted, leading to a decrease in resolution. In addition, if this heat shrinkage stress value occurs below 60°C, there is a tendency for the dimensional stability of the film to decrease and the resolution to decrease due to the enlargement of the pores, while if it occurs above 150°C, the perforation sensitivity decreases. This is not desirable as it tends to decrease.
【0018】さらに、フイルムの厚みは0.5〜6μm
、好ましくは1〜4μm、より好ましくは1.5〜2.
5μmである。この厚さが、0.5μm未満の場合、強
度が不足し剥離層の剥離時の穿孔時に破損しやすくなる
傾向があり、6μmを越える場合、感度が低下し穿孔が
不十分になる傾向がある。さらにフイルム用の熱可塑性
樹脂としては、重縮合系樹脂、ビニル系樹脂、オレフィ
ン系樹脂等の各樹脂が用いられるが、安定的に延伸加工
し、生産性良く製造するためには、ポリエステル系樹脂
、ポリアミド系樹脂、塩化ビニル系樹脂、塩化ビニリデ
ン系樹脂、ポリエチレン系樹脂、ポリプロピレン系樹脂
等が好ましい。さらに、製版の際のフイルム溶融収縮特
性に由来する形状の整った孔を形成するためには、ポリ
エステル系樹脂が好ましい。ポリエステル系樹脂として
は、例えば、共重合ポリエステル系樹脂であり、ポリエ
ステルを構成するジカルボン酸成分とジオール成分のい
ずれか一方、またはその両方が2種以上の異なった成分
からなるものである。具体的には、異なったジカルボン
酸を用いる場合には、テレフタル酸と他のジカルボン酸
、例えば、イソフタル酸、フタル酸等の芳香族ジカルボ
ン酸や、芳香環にエステル化反応に寄与しない置換基を
有する芳香族ジカルボン酸、あるいはコハク酸、アジピ
ン酸等の脂肪族ジカルボン酸の組み合わせが用いられる
し、また、異なったジオール成分を用いる場合には、エ
チレングリコールと他のジオール類、例えば、プロピレ
ングリコール、ジエチレングリコール、1,4−ブタン
ジオール、1,5−ペンタンジオール、1,6−ヘキサ
ンジオール、ネオペンチルグリコール、ポリエチレング
リコール、ポリテトラメチレングリコール、シクロヘキ
サンジメタノール等の中から、適宜用いられる。Furthermore, the thickness of the film is 0.5 to 6 μm.
, preferably 1 to 4 μm, more preferably 1.5 to 2.
It is 5 μm. If this thickness is less than 0.5 μm, the strength is insufficient and tends to be easily damaged during perforation when peeling off the release layer, and if it exceeds 6 μm, sensitivity tends to decrease and perforation tends to be insufficient. . Furthermore, various resins such as polycondensation resins, vinyl resins, and olefin resins are used as thermoplastic resins for films, but in order to stably stretch and manufacture with high productivity, polyester resins are used. , polyamide resin, vinyl chloride resin, vinylidene chloride resin, polyethylene resin, polypropylene resin, etc. are preferable. Further, in order to form well-shaped pores due to film melting and shrinkage characteristics during plate making, polyester resins are preferred. The polyester resin is, for example, a copolymerized polyester resin, and one or both of the dicarboxylic acid component and the diol component constituting the polyester are composed of two or more different components. Specifically, when using different dicarboxylic acids, terephthalic acid and other dicarboxylic acids, such as aromatic dicarboxylic acids such as isophthalic acid and phthalic acid, or substituents that do not contribute to the esterification reaction on the aromatic ring are used. or a combination of aliphatic dicarboxylic acids such as succinic acid and adipic acid, and when using different diol components, ethylene glycol and other diols, such as propylene glycol, The diethylene glycol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, neopentyl glycol, polyethylene glycol, polytetramethylene glycol, cyclohexanedimethanol, etc. are used as appropriate.
【0019】好ましい共重合ポリエステル系樹脂として
は、例えば、ジオール成分としてエチレングリコールを
主体とし、1,4−シクロヘキサンジメタノールを40
モル%以下、好ましくは20〜40モル%、さらに好ま
しくは25から35モル%を含有するものを用い、これ
とテレフタル酸とを重縮合させたものである。これらの
中でも特に、原料樹脂として充分アニーリングして平衡
状態としたものの結晶化度(広角X線法による:理学電
機社製、ロータフレックスRU−200Bにて、グラフ
ァイト・モノクロメータを使用、印加電圧50kV、印
加電流160mA、ターゲットCu、測定角2θ=5〜
38゜)が30%以下のものが好適に用いられ、好まし
くは20%以下、さらに好ましくは10%以下、特に好
ましくは5%以下の実質的に非晶質のものである。この
特に好ましい樹脂として、ジカルボン酸成分としてテレ
フタル酸を主成分としたものを用い、ジオール成分とし
てエチレングリコール約70モル%、1,4−シクロヘ
キサンジメタノール約30モル%の混合物を用いて共重
合したものがある。[0019] A preferred copolyester resin is, for example, mainly composed of ethylene glycol as the diol component and 40% of 1,4-cyclohexanedimethanol.
It is polycondensed with terephthalic acid using a compound containing mol % or less, preferably 20 to 40 mol %, more preferably 25 to 35 mol %. Among these, the crystallinity of the raw material resin that has been sufficiently annealed to reach an equilibrium state (by wide-angle X-ray method: Rotaflex RU-200B manufactured by Rigaku Denki Co., Ltd. using a graphite monochromator, applied voltage 50 kV) , applied current 160 mA, target Cu, measurement angle 2θ = 5 ~
38°) of 30% or less is suitably used, preferably 20% or less, more preferably 10% or less, particularly preferably 5% or less and is substantially amorphous. This particularly preferred resin was copolymerized using a resin mainly composed of terephthalic acid as the dicarboxylic acid component and a mixture of about 70 mol% ethylene glycol and about 30 mol% 1,4-cyclohexanedimethanol as the diol component. There is something.
【0020】さらに該層には、必要な特性をそこなわな
い範囲で、他の重合体、オリゴマーを配合することがで
き、また、各種の添加剤、例えば、酸化防止剤、熱安定
剤、可塑剤、滑剤等を目的に応じて配合することができ
る。また、本発明の原紙で用いられる支持体とは、印刷
インクの透過が可能で、製版時に実質的に熱変形を起こ
さない天然繊維、再生繊維、合成繊維等の単体またはこ
れらを混合したものを原料とした、薄葉紙、不織布等の
多孔質体であり、坪量4〜20g/m2 のものが好適
に用いられる、好ましくは、6〜15g/m2 、より
好ましくは8〜12g/m2 である。[0020] Furthermore, other polymers and oligomers can be blended in the layer within a range that does not impair the necessary properties, and various additives such as antioxidants, heat stabilizers, plasticizers, etc. Agents, lubricants, etc. can be added depending on the purpose. Furthermore, the support used in the base paper of the present invention is made of natural fibers, recycled fibers, synthetic fibers, etc. alone or a mixture of these fibers, which are permeable to printing ink and do not substantially undergo thermal deformation during plate making. A porous material such as tissue paper or nonwoven fabric is used as a raw material, and a basis weight of 4 to 20 g/m2 is suitably used, preferably 6 to 15 g/m2, more preferably 8 to 12 g/m2.
【0021】[0021]
【実施例】以下に実施例により本発明を更に詳しく説明
するが、本発明はこれらの例に限定されるものではない
。EXAMPLES The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited to these Examples.
【0022】[0022]
【実施例1】まず、支持体である薄葉紙を下記の方法に
て作成した。濾水度18゜SR(JIS P−812
1)に叩解したマニラ麻を40重量%、濾水度25゜S
Rに叩解したサイザル麻を20重量%、0.1デニール
、長さ3mmのPET繊維を20重量%、0.3デニー
ル長さ3mmのビニロン繊維を20重量%とを、均一に
混合し、さらに、エポキシ化ポリアミドポリアミノ樹脂
を繊維に対して2%となるように水溶液にして添加し均
一に混合した。これを紙料として円網式抄紙機による湿
式抄紙法にて薄葉紙を得た。さらにこの薄葉紙に、グラ
ビア塗工機を用いて、水系エマルジョンタイプのウレタ
ン樹脂(第一工業製薬(株)製、スーパーフレックス1
00)を、塗工量0.8g/m2 となるように塗工し
、坪量10.9g/m2 、厚さ31.1μmの薄葉紙
を得て、原紙の支持体とした。[Example 1] First, a thin paper serving as a support was prepared by the following method. Freeness 18°SR (JIS P-812
1) 40% by weight of beaten Manila hemp, freeness 25°S
20% by weight of beaten sisal hemp, 20% by weight of PET fibers of 0.1 denier and 3 mm in length, and 20% by weight of vinylon fibers of 0.3 denier and 3 mm in length are uniformly mixed, and then An aqueous solution of epoxidized polyamide polyamino resin was added to the fiber at a concentration of 2% and mixed uniformly. This was used as paper stock to obtain thin paper using a wet paper making method using a cylinder paper machine. Furthermore, this thin paper was coated with a water-based emulsion type urethane resin (Superflex 1 manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) using a gravure coating machine.
00) was coated at a coating weight of 0.8 g/m2 to obtain thin paper having a basis weight of 10.9 g/m2 and a thickness of 31.1 μm, which was used as a base paper support.
【0023】次に、懸濁重合にて得られたメチルメタク
リレートを主成分とした共重合体粒子を、粒径分級用ふ
るいにて分級し、15〜25μmの粒径をもつ微粒子を
得た。この微粒子を酢酸ビニル系接着剤メタノール(コ
ニシ(株)KE−60)溶液に分散させ、酢酸ビニル固
形分0.6g/m2 の設定になるように、グラビアコ
ータにて、上記薄葉紙の樹脂塗工面に塗布し、その後溶
剤を飛散させ、微粒子が固着した支持体(15〜30個
/mm2 程度の密度で粒子が固着)を得た。Next, the copolymer particles containing methyl methacrylate as a main component obtained by suspension polymerization were classified using a particle size classification sieve to obtain fine particles having a particle size of 15 to 25 μm. The fine particles were dispersed in a vinyl acetate adhesive methanol solution (Konishi Co., Ltd. KE-60), and the resin-coated surface of the thin paper was coated with a gravure coater so that the vinyl acetate solid content was set at 0.6 g/m2. After that, the solvent was dispersed to obtain a support on which fine particles were fixed (particles were fixed at a density of about 15 to 30 pieces/mm 2 ).
【0024】一方、フイルムを下記方法にて作成した。
非晶性ポリエステル樹脂(イーストマン・ケミカル社製
、PETG6763樹脂、広角X線法による樹脂の結晶
化度は0%):Aと剥離剤としてポリオキシエチレン・
オレートを3重量%添加したエチレン・酢酸ビニル共重
合体、ポリプロピレン、エチレン・αオレフィン・エラ
ストマーよりなる混合物:Bとを多層状態(A/B/A
)でサーキュラーダイより押し出しし、バブル状で2軸
延伸後、フラット状で熱処理を行い、目的とする2μm
のポリエステルを両面に形成した多層フイルムを得た。
該ポリエステルフイルムの加熱収縮率は73%であり、
加熱収縮応力は360g/mm2 であった。On the other hand, a film was prepared by the following method. Amorphous polyester resin (manufactured by Eastman Chemical Co., PETG6763 resin, crystallinity of resin determined by wide-angle X-ray method is 0%): A and polyoxyethylene as a release agent.
A mixture of ethylene/vinyl acetate copolymer, polypropylene, and ethylene/α-olefin elastomer to which 3% by weight of oleate has been added: B and a multilayered state (A/B/A
) is extruded through a circular die, biaxially stretched in a bubble shape, and then heat treated in a flat shape to achieve the desired 2μm.
A multilayer film was obtained in which polyester was formed on both sides. The heat shrinkage rate of the polyester film is 73%,
The heat shrinkage stress was 360 g/mm2.
【0025】一方、接着剤を次のように処方した。エチ
レングリコールジグリシジルエーテル(ナガセ化成工業
(株)、デナコールEX−810)とポリアミドアミン
(三和化学工業(株)、サンマイド300)を、17:
83の重量比となるように調合し、イソプロピルアルコ
ールに溶解させた。まず、上記の微粒子固着支持体を巻
き出し機から繰り出し、接着剤が塗布量1.5g/m2
になるように接着剤溶液をグラビアコーターを用いて
この支持体に塗布した後、第2の巻き出し機から繰り出
した前出の多層フイルムに重ね合わせ、積合させた状態
で設定50℃の乾燥炉を通過させ、溶剤を蒸発乾燥させ
た後、この積層体を巻き取り機で巻き取った。さらに、
この原紙中間体を35℃、48時間エージングし、接着
を完了させた。エラストマー積層体から、フイルムと微
粒子固着支持体とが接着された原紙中間体を剥離し、そ
のフイルム表面にシリコンオイルを0.05g/m2
塗布し、熱融着防止性のオーバーコート層とし、最終的
な原紙を得た。On the other hand, an adhesive was formulated as follows. Ethylene glycol diglycidyl ether (Nagase Kasei Kogyo Co., Ltd., Denacol EX-810) and polyamide amine (Sanwa Kagaku Kogyo Co., Ltd., Sanmide 300), 17:
The mixture was prepared at a weight ratio of 83% and dissolved in isopropyl alcohol. First, the above-mentioned particulate fixed support was unrolled from the unwinding machine, and the adhesive was coated in an amount of 1.5 g/m2.
After applying the adhesive solution to this support using a gravure coater, it was superimposed on the aforementioned multilayer film fed out from the second unwinding machine, and dried at a setting of 50°C while stacked. After passing through an oven and evaporating the solvent to dryness, the laminate was wound up with a winder. moreover,
This base paper intermediate was aged at 35° C. for 48 hours to complete adhesion. The base paper intermediate to which the film and fine particle adhesion support were adhered was peeled off from the elastomer laminate, and 0.05 g/m2 of silicone oil was applied to the surface of the film.
This was applied to form an overcoat layer with anti-thermal adhesion properties, and the final base paper was obtained.
【0026】次に、400ドット/インチ(素子間ピッ
チ:63.5μm)の素子密度で、素子サイズ(主走差
方向幅×副走差方向長)が50μm×45μmであるサ
ーマルヘッドを、サーマルヘッド試験用印字装置((株
)大倉電機製、PH−TMD)に搭載し、黒ベタや文字
等のパターンが印刷できるように、上記の原紙を製版し
た。この製版後の原紙を顕微鏡観察したところ、黒ベタ
文字等のパターン部の孔は、サーマルヘッドの素子に対
応して独立に形成されていることが判った。さらに、こ
の原紙を全自動デジタル孔版印刷機(理想科学工業(株
)製、リソグラフRC115)のドラムに装着し、80
枚/分の印刷速度で印刷し得られた印刷物は、白抜けも
少なく、非常に鮮明なものであった。Next, a thermal head with an element density of 400 dots/inch (interelement pitch: 63.5 μm) and an element size (main scanning direction width x sub scanning direction length) of 50 μm x 45 μm was heated. The above-mentioned base paper was made into a plate so that it could be installed in a head test printing device (manufactured by Okura Electric Co., Ltd., PH-TMD) and print patterns such as solid black and letters. When the base paper after plate making was observed under a microscope, it was found that holes in pattern areas such as solid black characters were formed independently corresponding to the elements of the thermal head. Furthermore, this base paper was mounted on the drum of a fully automatic digital stencil printing machine (Risograph RC115, manufactured by Riso Kagaku Kogyo Co., Ltd.), and
The printed matter printed at a printing speed of one sheet per minute was very clear with few white spots.
【0027】[0027]
【比較例1】実施例1で得られた薄葉紙を微粒子固着処
理をせずそのまま支持体として用い実施例1と同じフイ
ルム、方法を用いて原紙を作成した。さらに実施例1と
同様の方法にて、製版した原紙を顕微鏡観察したところ
、黒ベタ部や文字等のパターン部の孔は、薄葉紙の繊維
接着部に対応した不織布のフイルムが穿孔されず、サー
マルヘッドの素子に対応して独立に形成されていなかっ
た。さらに、実施例1と同様の方法にて得られた印刷物
は、薄葉紙の繊維に由来する白抜けが、実施例1の印刷
物に比べると目立っていた。[Comparative Example 1] A base paper was prepared using the same film and method as in Example 1, using the thin paper obtained in Example 1 as a support without undergoing fine particle fixation treatment. Furthermore, when the base paper made by the same method as in Example 1 was observed under a microscope, it was found that the holes in the black solid areas and pattern areas such as letters were not perforated in the nonwoven fabric film corresponding to the fiber bonded areas of the tissue paper, and were thermally damaged. They were not formed independently to correspond to the elements of the head. Further, in the printed matter obtained by the same method as in Example 1, white spots originating from the fibers of the thin paper were more noticeable than in the printed matter of Example 1.
【0028】[0028]
【発明の効果】本発明の原紙では、フイルムと支持体と
が主として微粒子を介して接着されているので、フイル
ムの接着固定される部分がより小さい面積となるため、
フイルムが熱製版されるときにフイルムの穿孔を支持体
が阻害する影響が、従来の原紙に比べ著しく少なくなる
ため、フイルムの開孔状態が均一なものとなる。しかも
、従来の原紙では避けられなかった、支持体繊維の結束
部でのフイルム穿孔阻害とインク透過阻害に由来する、
印刷物の黒ベタ部での白抜けが、著しく減少することに
なる。Effects of the Invention In the base paper of the present invention, since the film and the support are bonded mainly through fine particles, the area where the film is bonded and fixed becomes smaller.
When the film is thermally engraved, the effect of the support on the perforation of the film is significantly reduced compared to conventional base paper, so that the perforation state of the film becomes uniform. Moreover, this is due to the inhibition of film perforation and inhibition of ink permeation at the binding part of the support fibers, which was unavoidable with conventional base paper.
White spots in solid black areas of printed matter are significantly reduced.
Claims (1)
質支持体を貼り合せてなる感熱孔版印刷用原紙において
、接着層に50μm以下の微粒子が存在することを特徴
とする感熱孔版印刷用原紙。1. A base paper for heat-sensitive stencil printing comprising a thermoplastic film and an ink-permeable porous support bonded together, characterized in that fine particles of 50 μm or less are present in the adhesive layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5230591A JPH04288288A (en) | 1991-03-18 | 1991-03-18 | Base paper for thermal screen printing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5230591A JPH04288288A (en) | 1991-03-18 | 1991-03-18 | Base paper for thermal screen printing |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04288288A true JPH04288288A (en) | 1992-10-13 |
Family
ID=12911076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5230591A Withdrawn JPH04288288A (en) | 1991-03-18 | 1991-03-18 | Base paper for thermal screen printing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04288288A (en) |
-
1991
- 1991-03-18 JP JP5230591A patent/JPH04288288A/en not_active Withdrawn
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