JPH02235653A - Image recording and its apparatus - Google Patents
Image recording and its apparatusInfo
- Publication number
- JPH02235653A JPH02235653A JP1057455A JP5745589A JPH02235653A JP H02235653 A JPH02235653 A JP H02235653A JP 1057455 A JP1057455 A JP 1057455A JP 5745589 A JP5745589 A JP 5745589A JP H02235653 A JPH02235653 A JP H02235653A
- Authority
- JP
- Japan
- Prior art keywords
- gel
- electrode
- image
- layer
- material 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.)
- Granted
Links
- 239000000463 material Substances 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 23
- 239000012530 fluid Substances 0.000 claims description 20
- 239000003086 colorant Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 13
- 230000005611 electricity Effects 0.000 claims description 5
- 230000001154 acute effect Effects 0.000 claims description 4
- 238000009751 slip forming Methods 0.000 claims 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 abstract description 9
- 229910052737 gold Inorganic materials 0.000 abstract description 9
- 239000010931 gold Substances 0.000 abstract description 9
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract description 8
- 239000004020 conductor Substances 0.000 abstract description 7
- 239000006229 carbon black Substances 0.000 abstract description 5
- 229910052697 platinum Inorganic materials 0.000 abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052799 carbon Inorganic materials 0.000 abstract description 2
- 239000000843 powder Substances 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract 1
- -1 borate ions Chemical class 0.000 description 34
- 235000021251 pulses Nutrition 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 8
- 239000004327 boric acid Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- 229920001477 hydrophilic polymer Polymers 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920006289 polycarbonate film Polymers 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229920002120 photoresistant polymer Polymers 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- PJDOLCGOTSNFJM-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctan-1-ol Chemical compound OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F PJDOLCGOTSNFJM-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- DWDURZSYQTXVIN-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-methyliminocyclohexa-2,5-dien-1-ylidene)methyl]aniline Chemical compound C1=CC(=NC)C=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 DWDURZSYQTXVIN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- AUNAPVYQLLNFOI-UHFFFAOYSA-L [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O Chemical compound [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O AUNAPVYQLLNFOI-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- JPIYZTWMUGTEHX-UHFFFAOYSA-N auramine O free base Chemical compound C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 JPIYZTWMUGTEHX-UHFFFAOYSA-N 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 125000005501 benzalkonium group Chemical class 0.000 description 1
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000012730 carminic acid Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- PJQYNUFEEZFYIS-UHFFFAOYSA-N perylene maroon Chemical compound C=12C3=CC=C(C(N(C)C4=O)=O)C2=C4C=CC=1C1=CC=C2C(=O)N(C)C(=O)C4=CC=C3C1=C42 PJQYNUFEEZFYIS-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 229940051201 quinoline yellow Drugs 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001059 synthetic polymer Chemical class 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(II) oxide Inorganic materials [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Electronic Switches (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Duplication Or Marking (AREA)
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は画像記録方法及び装置に関し、詳しくは、コン
ピューター、ワードプロセッサーなどの出力を記録した
り,ファクシミリ等のデジタル通信における出力を記録
したりするのに有用であって、特に、これらの高密度か
つ高速記録が行なえる画像記録方法及び装置に関する.
〔従来技術〕
事務用機器における画像記録方法ないし装置には、大別
して、インパクト方式のもの及びノンインパクト方式の
ものが知られている。そして、後者のノンインパクト記
録方式は、記録時の騒音が少ないという理由から、ワー
プロ、パソコンなどのハードコピー装置として大いに関
心がもたれ利用に供されるようになっている.このノン
インパクト記録方法又は装置(特に断オ〕らない限り単
に「記録方法」あるいは「画像記録方法」又は『記録装
置」あるいは[画像記録装置]と称する)にはインクジ
ェットプリンター熱転写プリンターをはじめとして多く
が知られているが、近時は、ポリビニルアルコールー硼
酸ゲルにみられる架橋構造が通電で破壊される呪象[八
eLLoezalo、φ等により[ポリビニルアルコー
ルの電着機構の研究J kollojdn.ZH, 4
6,771(1984)&.:記載されテイル]を利用
した記録方式が注目されている(特開昭63−3027
9号公報など)。[Detailed Description of the Invention] [Technical Field] The present invention relates to an image recording method and apparatus, and more specifically, it is useful for recording the output of computers, word processors, etc., and for recording the output of digital communications such as facsimiles. In particular, the present invention relates to an image recording method and apparatus capable of performing high-density and high-speed recording.
[Prior Art] Image recording methods and devices for office equipment are broadly classified into impact type and non-impact type. The latter non-impact recording method has attracted much attention and is now being used in hard copy devices such as word processors and personal computers because it produces less noise during recording. This non-impact recording method or device (simply referred to as a "recording method" or "image recording method" or "recording device" or "image recording device" unless otherwise specified) includes many types including inkjet printers and thermal transfer printers. However, recently, a phenomenon in which the crosslinked structure observed in polyvinyl alcohol-boric acid gel is destroyed by energization [8eLLoezalo, φ et al. [Research on the electrodeposition mechanism of polyvinyl alcohol J. Kollojdn. ZH, 4
6,771 (1984) &. : A recording method using the written tail is attracting attention (Japanese Patent Application Laid-Open No. 63-3027
Publication No. 9, etc.).
この特開昭63−30279号公報等においで開示され
ている手段は、親水性高分子を硼酸で架橋した構成物中
に着色剤を分散した流動性インクを用い、このインクに
エネルギーを印加してインクの付着性を変化させ、これ
を中間転写媒体もしくはフィルム等の被記録材に転写し
7、更に、これを普通紙などに転写して画像形成を行な
うという、低ランニングコストで低エネルギーの記録方
式であり、これによれば従来の熱転写記録方式の欠点で
あるランニングコストを低減させ、カラー化も容易にな
し得るといった効果がもたらされる.
しかしながら、例えば特開昭63−290773号公報
に記載されているような電極で記録を行なうと、その電
極に流動化したインクが付着し、通電終了後に電極に付
着したインクが基体上のゲル層に逆転写され、これが被
転写媒体に転写されて画像に″尾引き″の現象が時とし
て生じる.〔目 的〕
本発明の第1の目的は、通電により架橋構造が変化し流
動性を生じる(流動性が変化する)インクを用いて繰返
し記1[行なっても尾引きのない安定した画像が得られ
る(殊に高速記録を行なっても安定した画像が得られる
)記録方法及び装置を提供するものである.本発明の第
2の目的は操作が簡単で、製造コストが安く、保守の容
易な画像記録方法及び装置を提供するものである.
〔構 成〕
本発明の第1は、基体表面に着色剤を含み通電により流
動性となるゲル状物質層を設け、そのゲル状物質層に画
像信号に従って電極により通電した後,通電後の流動性
となった着色物質を選択的に被転写媒体に転写せしめる
画像記録装置において、前記電極の少なくとも片面に臨
界表面張力35dyne/cm(20℃)以下の材料を
接合せしめたことを特徴としている.
本発明の第2は、基体表面に着色剤を含み通電により流
動性となるゲル状物質層を設け,そのゲル状物質層に画
像信号に従って電極により通電した後、通電後の流動性
となった着色物質を選択的に被転写媒体に転写せしめる
画像記録装置において、前記電極のゲル状物質層に接す
る部分の近傍を鋭角にしたことを特徴としている。The method disclosed in JP-A No. 63-30279 uses a fluid ink in which a colorant is dispersed in a composition in which a hydrophilic polymer is cross-linked with boric acid, and energy is applied to this ink. This is a low-running, low-energy method that changes the adhesion of the ink and transfers it to a recording material such as an intermediate transfer medium or film7, and then transfers it to plain paper to form an image. This is a recording method that reduces running costs, which are disadvantages of conventional thermal transfer recording methods, and can easily produce color. However, when recording is performed using an electrode such as that described in JP-A No. 63-290773, fluidized ink adheres to the electrode, and after energization ends, the ink adhered to the electrode forms a gel layer on the substrate. This is reversely transferred to the transfer medium, and this sometimes causes the phenomenon of "tailing" on the image. [Purpose] The first object of the present invention is to produce a stable image without trailing even if the repeating process 1 is carried out using an ink whose crosslinked structure changes when energized and becomes fluid (fluidity changes). The object of the present invention is to provide a recording method and apparatus that can obtain stable images (particularly stable images even during high-speed recording). A second object of the present invention is to provide an image recording method and apparatus that are easy to operate, inexpensive to manufacture, and easy to maintain. [Structure] The first aspect of the present invention is to provide a layer of gel-like material that contains a colorant and becomes fluid when energized on the surface of a substrate, and after energizing the gel-like material layer with an electrode according to an image signal, the fluidity after energization is The image recording apparatus selectively transfers a colored substance that has become a color to a transfer medium, characterized in that a material having a critical surface tension of 35 dyne/cm (20° C.) or less is bonded to at least one side of the electrode. The second aspect of the present invention is to provide a gel-like material layer on the surface of the substrate that contains a colorant and becomes fluid when energized, and after energizing the gel-like material layer with an electrode according to an image signal, it becomes fluid after energization. An image recording apparatus that selectively transfers a colored substance to a transfer medium is characterized in that a portion of the electrode in contact with a gel-like substance layer has an acute angle.
本発明の第3は、基体表面に着色剤を含み通電により流
動性となるゲル状物質層を設け、そのゲル状物質層に画
像信号に従って電極により通電した後、通電後の流動性
となった着色物質を選択的に被転写媒体に転写せしめる
画像記録方法において、前記の基体と電極とを相対的に
移動せしめて通電を行なう際に、一画素を形成する為に
、基体表面のゲル状物質層外周が連続的に周速Vで移動
され、電極とゲル状物質層との接触幅が送り方向にWで
あり、目襟とする送り方向の画素幅をWとしたとき、式
W − w
t =
■
により導かれるtの値の40〜95%の時間通電するこ
とを特徴としている.
ちなみに、本発明者らは、インク層に通電を行ない、陽
極近傍のインク層を流動状態として、これをボンド紙、
コピー用紙等の普通紙に転写することのできる記録方法
及び装置についていろいろ研究・検討を貢なったところ
、■インクとして着色剤を含み通電により架橋構造が変
化して流動性を生じる(流動性が変化する)ような性質
のものを使用し,かつ、■インク層に通電するのに際し
て電極に工夫をこらすことによって、またそれとは別に
、相対的に電極とインク層とが移動している場合にあっ
ての通電時間をある範囲に収めるようにすれば、尾引き
の生じない良質の画像記録が得られることを確めた.本
発明はこれに基づいてなされたものである.以下に、本
発明方法及び装置を添付の図面に従いながらさらに詳細
に説明する。The third aspect of the present invention is to provide a gel-like material layer on the surface of the substrate that contains a colorant and becomes fluid when energized, and after energizing the gel-like material layer with an electrode according to an image signal, the layer becomes fluid after energization. In an image recording method in which a colored substance is selectively transferred to a transfer medium, when the substrate and the electrode are moved relative to each other and energized, a gel-like substance on the surface of the substrate is used to form one pixel. When the outer periphery of the layer is continuously moved at a circumferential speed V, the contact width between the electrode and the gel-like material layer is W in the feeding direction, and the pixel width in the feeding direction is W, the formula W − w It is characterized by being energized for 40 to 95% of the time of the value of t derived from t = ■. Incidentally, the present inventors applied electricity to the ink layer to bring the ink layer near the anode into a fluid state, and transferred it to bond paper,
After conducting various research and studies on recording methods and devices that can be used to transfer images onto plain paper such as copy paper, we found that: (1) The ink contains a colorant, and when energized, the crosslinked structure changes and becomes fluid. By using materials with properties that change (change), and by devising the electrode when applying electricity to the ink layer, and separately, when the electrode and the ink layer are moving relative to each other, It was confirmed that by keeping the energization time within a certain range, high-quality image recording without trailing could be obtained. The present invention has been made based on this. In the following, the method and apparatus of the present invention will be explained in more detail with reference to the accompanying drawings.
第1図は本発明方法の実施に有効な装置の代表的な一例
の全体を示した概略図である.図中、5は基体ベルト1
2の表面にゲル状インク層(通電前は非流動性であり通
電により流動性となるインク層)13を有するゲル状層
保持ベルトである(第2図).
基体ベルトl2は導電性であって、例えばニッケル等の
金属ベルト、ニッケル表面に金、白金等などをメッキし
たもの、ポリエステル等の樹脂にカーボンブラックのご
とき導電性物質を分散したもの、ポリエステル等の樹脂
のベルト表面に金,白金、SnOなどの導電性材料を真
空蒸着等の方法により設けたもの、等が例示できる.イ
ンク層13は着色剤を含み通電により流動性が変化する
非流動性のゲル状着色物質(親水性高分子及び着色剤を
主成分としてなる)により構成されるものである6
これらゲル状物質は水酸基を有する水溶性高分子化合物
を硼酸イオンにより架橋することにより得ることができ
る.
ここで、親水性高分子(水溶性高分子化合物)としては
ロー力ストビーンガムやグーアガム,ペクチン等の多糖
類およびカラギーナン等の電解質多糖類、また、ポリビ
ニルアルコール等の水酸基を有する合成高分子化合物が
挙げられる。FIG. 1 is a schematic diagram showing the entirety of a typical example of an apparatus effective for carrying out the method of the present invention. In the figure, 5 is the base belt 1
This is a gel-like layer holding belt having a gel-like ink layer 13 (an ink layer that is non-fluid before energization and becomes fluid when energized) on the surface of 2 (Fig. 2). The base belt l2 is electrically conductive, and includes, for example, a metal belt made of nickel or the like, a nickel surface plated with gold, platinum, etc., a resin such as polyester in which a conductive substance such as carbon black is dispersed, or a belt made of polyester or the like. Examples include those in which a conductive material such as gold, platinum, or SnO is provided on the surface of a resin belt by a method such as vacuum deposition. The ink layer 13 is composed of a non-fluid gel-like coloring substance (mainly composed of a hydrophilic polymer and a colorant) that contains a colorant and whose fluidity changes when energized.6 These gel-like substances are It can be obtained by crosslinking a water-soluble polymer compound containing hydroxyl groups with borate ions. Here, examples of hydrophilic polymers (water-soluble polymer compounds) include polysaccharides such as low-strength bean gum, guar gum, and pectin, electrolyte polysaccharides such as carrageenan, and synthetic polymer compounds having hydroxyl groups such as polyvinyl alcohol. It will be done.
これら親水性高分子を架橋する硼酸イオンは,硼酸、硼
砂などの硼酸イオン源化合物を水に溶解することにより
得られる。The boric acid ions that crosslink these hydrophilic polymers can be obtained by dissolving a boric acid ion source compound such as boric acid or borax in water.
親水性高分子は単独あるいは複数組み合わせて用いられ
るが、インク層13への含有率はその分子量や溶液粘度
に関係するが,通常1重量%から20重量%用いること
が好ましい.一方,これを架橋する硼酸イオンの添加量
は、少なくともインク層13が常温ではゲル融点に達し
ない非流動性を保つのに必要な量で使用されることが好
ましい.具体的には,硼酸イオン源となる硼酸、硼砂な
どの添加量としては親水性高分子の架橋可能な水酸基数
に対して4分の1当量以上の量を添加することが好まし
く,硼酸イオン量によりゲルの架橋密度が高まりゲルの
強度が高まる.硼酸を用いる場合は同時にアルカリ水酸
化物の添加を行なうことによりゲル化が有効に行なえる
.
インク層l3には更に着色剤が含まれる.着色剤として
はカラーインデックスに酸性染料,直接染料、塩基性染
料として記載されているような水溶性染料を用いること
も出来るが、このような染料を用いると僅かに水分が被
転写体に転写されても染料も同時に転写されるため地肌
が汚れ易く、特に中間転写体のごときものを用いること
なく,第1図に示したように、直接インク層13と記録
紙2とを接触せしめるような装置においてはその傾向が
著しくなる.従って,着色剤としては顔料,油溶性染料
,分散性染料等水に不用なものを用いることが好ましい
.これらの着色剤の例としてはカーボンブラック,四三
酸化鉄、チタンブラック、チタンイエロー、モリブデン
赤、ジンクク口メート等の無機顔料、フタロシアニンブ
ルー、ブリリアントカーミンレーキ、パーマネントレッ
ドレーキ.オーラミンレーキ、ローダミンレーキ.メチ
ルバイオレットレーキ,キノリンイエローレーキ、マラ
カイトグリーンレーキ、イソインドリノン、キナクリド
ン、ペリノンオレンジ、ペリレンスカーレット、ペリレ
ンマルーン等の有機顔料を挙げることが出来る。油性染
料、分散性染料についてはカラーインデックス(The
Soeiクtv ofDyers and Colo
urists 19’N)を参照し、色調に優れたもの
,耐光性に優れたもの、耐熱性に優れたちの等を要求に
応じて選定することが出来る.これらの着色剤はインク
層の0.2〜20重量%となるように添加することが好
ましい.インク層13の形成液調製は液体媒体として主
に水を用いることが出来るが、インク層13からの水分
の蒸発を防止したり,インク層13の流動性をコントロ
ールしたりするために、エチレングリコール、ジエチレ
ングリコール、テトラエチレングリコール、ポリエチレ
ングリコール、プロピレングリコール,ジブロビレング
リコール、グリセリン等の多価アルコール類;ジェチレ
ングリコールモノエチルエーテル、ジエチレングリコー
ルモノブチルエーテル、エチレングリコールモノメチル
エーテル等前記多価アルコールのエーテル類;N−メチ
ル−2−ピロリドン、l,3−ジメチルイミダゾリジノ
ン等を用いることが出来る。The hydrophilic polymers may be used alone or in combination, and the content in the ink layer 13 is related to its molecular weight and solution viscosity, but it is usually preferable to use 1% to 20% by weight. On the other hand, it is preferable that the amount of boric acid ions added to crosslink the ink layer 13 is at least the amount necessary to maintain non-fluidity of the ink layer 13, which does not reach the gel melting point at room temperature. Specifically, the amount of boric acid, borax, etc. to be added as a source of boric acid ions is preferably one-quarter equivalent or more based on the number of crosslinkable hydroxyl groups in the hydrophilic polymer. This increases the crosslinking density of the gel and increases its strength. When using boric acid, gelation can be effectively achieved by simultaneously adding an alkali hydroxide. The ink layer l3 further contains a colorant. As a coloring agent, water-soluble dyes such as those listed in the Color Index as acid dyes, direct dyes, and basic dyes can also be used, but when such dyes are used, a small amount of water may be transferred to the transferred material. However, since the dye is also transferred at the same time, the background is easily smudged.In particular, an apparatus that brings the ink layer 13 into direct contact with the recording paper 2 as shown in FIG. This tendency becomes more pronounced. Therefore, it is preferable to use colorants that are unnecessary for water, such as pigments, oil-soluble dyes, and dispersible dyes. Examples of these colorants include carbon black, triiron tetroxide, titanium black, titanium yellow, molybdenum red, inorganic pigments such as zinc mate, phthalocyanine blue, brilliant carmine lake, and permanent red lake. Auramine Lake, Rhodamine Lake. Examples include organic pigments such as methyl violet lake, quinoline yellow lake, malachite green lake, isoindolinone, quinacridone, perinone orange, perylene scarlet, and perylene maroon. For oil-based dyes and disperse dyes, see the Color Index (The
TV of Dyers and Colo
urists 19'N) and select those with excellent color tone, excellent light resistance, excellent heat resistance, etc., according to your needs. These colorants are preferably added in an amount of 0.2 to 20% by weight of the ink layer. Water can be mainly used as a liquid medium to prepare the liquid for forming the ink layer 13, but ethylene glycol can be used to prevent the evaporation of water from the ink layer 13 and to control the fluidity of the ink layer 13. , diethylene glycol, tetraethylene glycol, polyethylene glycol, propylene glycol, dibrobylene glycol, glycerin, and other polyhydric alcohols; diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether, and other polyhydric alcohol ethers; N-methyl-2-pyrrolidone, 1,3-dimethylimidazolidinone, etc. can be used.
更に、着色剤の分散性を良好にするため等の理由でカチ
オン系,アニオン系又はノニオン系の界面活性剤を添加
することが出来る。具体的には、ポリオキシエチレンア
ルキルエーテル類、ポリオキシエチレンアルキルフェニ
ルエーテル類、ポリオキシエチレンアルキルエステル類
、ポリオキシエチレンアルキルソルビタンエステル類、
ポリオキシエチレンアルキルアミン類,グリセリン脂肪
酸エステル類,ソルビタン脂肪酸エステル類、プロピレ
ングリコール脂肪酸エステル類、ポリオキシエチレング
リコール脂肪酸エステル類等のノニオン系界面活性剤;
アルキル硫酸塩類、ポリオキシエチレンアルキルエーテ
ル硫酸塩類、ポリオキシエチレンアルキルエーテル酢酸
類、アルキルベンゼンスルフオン酸塩類、N−アシルア
ミノ酸塩類、アルキルスルホコハク酸塩類、アルキルリ
ン酸塩類等の陰イオン型界面活性剤;ベンザルコニウム
塩のごとき第4級アミン類等の陽イオン型界面活性剤;
パーフルオロアルキルリン酸エステル類、バーフルオロ
アルキルカルボン酸塩類,パーフルオロ゛7ルキルベタ
イン類等のフッ素系界面活性剤等を挙げることが出来る
。Furthermore, a cationic, anionic or nonionic surfactant may be added for reasons such as improving the dispersibility of the colorant. Specifically, polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenyl ethers, polyoxyethylene alkyl esters, polyoxyethylene alkyl sorbitan esters,
Nonionic surfactants such as polyoxyethylene alkyl amines, glycerin fatty acid esters, sorbitan fatty acid esters, propylene glycol fatty acid esters, polyoxyethylene glycol fatty acid esters;
Anionic surfactants such as alkyl sulfates, polyoxyethylene alkyl ether sulfates, polyoxyethylene alkyl ether acetic acids, alkylbenzene sulfonates, N-acylamino acid salts, alkyl sulfosuccinates, alkyl phosphates; Cationic surfactants such as quaternary amines such as benzalkonium salts;
Examples include fluorine-based surfactants such as perfluoroalkyl phosphates, perfluoroalkyl carboxylic acid salts, and perfluoro7-alkyl betaines.
更に,インク層I3には必要に応じて、防腐剤、粘度調
整剤、表面張力調整剤、紫外線吸収剤、…調整剤等脊添
加することが出来る.
さて、第1図において、6は電極(陽極)であり、この
電極には画像信号に従ったパルス電圧4が印加されるが
、電極6はゲル状層保持ベルト5上のインク層13と接
触するように配置されている,20は他の電極(陰極=
帰路電極)であり、この電極はベルト搬送ローラ8aと
接触するように配置されているが,インク層l3又は基
体ベルト(導電性基体)12は接触するようにされてい
てもかまわない。但し、電極20は常時アース電位に保
たれるようになっている,電流密度は電極6とインク層
13との接触点においてインク層13の他の部分より著
しく大きくなることになり、前記接触点近傍のインク層
のみが流動性の変化を受ける。Furthermore, if necessary, preservatives, viscosity modifiers, surface tension modifiers, ultraviolet absorbers, etc. modifiers can be added to the ink layer I3. Now, in FIG. 1, 6 is an electrode (anode), and a pulse voltage 4 according to an image signal is applied to this electrode. 20 is the other electrode (cathode =
This electrode is placed in contact with the belt conveying roller 8a, but may be in contact with the ink layer l3 or the base belt (conductive base) 12. However, since the electrode 20 is always kept at ground potential, the current density will be significantly higher at the contact point between the electrode 6 and the ink layer 13 than at other parts of the ink layer 13. Only the nearby ink layer undergoes a change in fluidity.
2は記録紙であり,送りローラー10及びldにより転
写部に・搬送され、送りローラー】a及び1bによって
転写部から排出される,この間、記録紙2は記録紙押え
板7とインク層13との間の微小な間隙に挿入され、、
流動性変化を受けたインク層13と接触する。この接触
により流動性の高い部分(インク)はインク層13から
記録紙2へ転写されるため、ここに画像が形成される。Recording paper 2 is conveyed to the transfer section by feed rollers 10 and ld, and discharged from the transfer section by feed rollers a and 1b. inserted into the tiny gap between
It comes into contact with the ink layer 13 that has undergone a change in fluidity. Due to this contact, the highly fluid portion (ink) is transferred from the ink layer 13 to the recording paper 2, so that an image is formed there.
3は赤外線ランプであり、ゲル状層保持ベルト5に近接
して配置され転写後のインク層13を加熱することによ
り、通電がなされたところ、なされなかったところから
生じたインク層13の凹凸を溶融により平滑化するもの
である。本発明でのインク層13は加熱によっても流゛
動性が変化する特性を有している.赤外線ランプ3に代
えて、又は、これと併用して、基体ベルトの背面に接す
るか近接してヒーターを配置させることもできる.
14の破線で囲まれた部分はインク供給部であり,通常
,インク塗布ローラ10はゲル状層保持ベルト5から離
れた位置にあるが、或る程度の数の複写物が形成されて
ゲル状層保持ベルト5のインク層13の厚さが薄くなっ
た時にインク塗布ローラ10が図示されていないヒータ
ーにより加熱され、ゲル状層保持ベルト5に圧接する位
置に移動するように工夫されている.ゲル状インク9は
インク塗布ローラ10により加熱されて流動化しゲル状
層保持ベルト5に塗布される.図中、9aはゲル状イン
ク9の容器、11は受皿,12はスクイズローラである
.なお、容器9a内であってゲル状インク9の上部には
適当な重しを乗せておくのが望ましい.
さきに触れたように、第1図に示した画像記録装置にお
いて通常用いら九でいるスタイラスを用いて記録を行な
うと画像に尾引きを生じることがある.
第3図および第4図は本発明に係る電極構造の二例を示
すものである. 15(a)及び(b)はポリテトラフ
ルオロエチレン、ポリトリフルオロエチレン、ポリへキ
サルフルオロプロピレン、ポリジメチルシロキサン,ボ
リフッ化ビニリデン、ベルフルオロオクタノールのメタ
クリル酸エステル,ポリエチレン等の低表面エネルギー
を有する材質で形成された部分である。ここにいう[低
表面エネルギーを有する、材質」とは、臨界表面張力3
5dyne/cm(20℃)以下の材料を意味している
.一方,16は導電体であって金,白金、導電性炭素、
カーボンブラックや金属粉を分散せしめたポリカーボネ
ート、ポリアクリル酸エステル等の高分子重合体等で構
成される。第3図、第4図において、(a)は電極の断
面を示すものであり、(b)は斜視図である。図中、A
面がインク層と接触する。Reference numeral 3 denotes an infrared lamp, which is placed close to the gel-like layer holding belt 5 and heats the ink layer 13 after transfer, thereby removing the unevenness of the ink layer 13 that occurs when electricity is applied or not. It is smoothed by melting. The ink layer 13 in the present invention has a characteristic that its fluidity changes even when heated. Instead of the infrared lamp 3, or in combination with it, a heater may be placed in contact with or in the vicinity of the back surface of the base belt. The part surrounded by the broken line 14 is an ink supply section, and although the ink application roller 10 is normally located at a distance from the gel-like layer holding belt 5, it is possible to form a gel-like layer by forming a certain number of copies. When the thickness of the ink layer 13 on the layer holding belt 5 becomes thin, the ink application roller 10 is heated by a heater (not shown) and moved to a position where it comes into pressure contact with the gel layer holding belt 5. The gel ink 9 is heated by an ink application roller 10 to be fluidized and applied to the gel layer holding belt 5. In the figure, 9a is a container for the gel ink 9, 11 is a saucer, and 12 is a squeeze roller. Note that it is desirable to place an appropriate weight on top of the gel ink 9 inside the container 9a. As mentioned earlier, when recording is performed using a stylus, which is not normally used in the image recording apparatus shown in FIG. 1, trailing may occur in the image. Figures 3 and 4 show two examples of electrode structures according to the present invention. 15(a) and (b) have low surface energy such as polytetrafluoroethylene, polytrifluoroethylene, polyhexalfluoropropylene, polydimethylsiloxane, polyvinylidene fluoride, methacrylic acid ester of perfluorooctanol, polyethylene, etc. It is a part made of material. The term "material with low surface energy" here refers to a material with a critical surface tension of 3.
This refers to materials with a density of 5 dyne/cm (20°C) or less. On the other hand, 16 is a conductor such as gold, platinum, conductive carbon,
It is composed of high molecular weight polymers such as polycarbonate and polyacrylic acid ester in which carbon black and metal powder are dispersed. In FIGS. 3 and 4, (a) shows a cross section of the electrode, and (b) is a perspective view. In the figure, A
The surface is in contact with the ink layer.
第5図、第6図、第7図の前記とは異なる電極構造を示
すものである。これらはいずれも断面図であり、ゲル状
層保持ベルト5上のインク層l3には図のように接し,
インク層13は矢印のような方向に搬送される.電極を
このようにゲル層に接する近傍部分を鋭角とするときに
は、導電体16を保持する部材17. 18は必ずしも
上述のような低表面エネルギーの材料を用いなくとも,
ガラス,セラミック、Sin,、ボリアミドのような高
表面エネルギーのものを用いても尾引きには効果がある
が,上述のような低表面エネルギーの素材を用いること
が更に好ましい.第8図に模式的に示したように、第1
図のベルト5が画像形成の際に画素毎にステップ送りさ
れることなく、連続的に外周の周速がVで駆動されてい
る時、電極とインク層13との接触幅が送り方向にWで
あるとし、目標とする送り方向の画素幅をWとしたとき
W−W
t= ・・・・・・・・・ (1)■
が導きだされる(tは通電時間)。This figure shows a different electrode structure from those shown in FIGS. 5, 6, and 7. These are all cross-sectional views, and the ink layer l3 on the gel layer holding belt 5 is in contact with the ink layer l3 as shown in the figure.
The ink layer 13 is transported in the direction of the arrow. When the electrode has an acute angle in the vicinity of the gel layer, the member 17 for holding the conductor 16. 18 does not necessarily require the use of low surface energy materials as mentioned above.
Although the use of materials with high surface energy such as glass, ceramic, sin, and boryamide is effective in reducing tailing, it is more preferable to use materials with low surface energy such as those mentioned above. As schematically shown in Figure 8, the first
When the belt 5 shown in the figure is not step-fed pixel by pixel during image formation and is continuously driven at a peripheral speed of V, the contact width between the electrode and the ink layer 13 is W in the feeding direction. When the target pixel width in the feed direction is W, W-W t= (1) ■ is derived (t is the energization time).
従って,いまインク層に8 dot/mtmの密度で流
動化した部分を形成したければ,Wが125μ閣となる
ように(1)式の条件すなわち通電時間を設定すること
が計算される.このような設定した時間だけ通電を行な
うと実際には所望の画素幅よりも大きくなってしまう.
これを防止するために計算上のtの40〜95%,より
好ましくは50〜90%の時間だけパルス電流を流すこ
とが効果的である.40%以下では所望の画素幅が得ら
れにくい。Therefore, if it is desired to form a fluidized part with a density of 8 dots/mtm in the ink layer, it is calculated that the conditions of equation (1), that is, the energization time, should be set so that W is 125μ. If the current is turned on for such a set time, the pixel width will actually become larger than the desired pixel width.
To prevent this, it is effective to flow the pulse current for a period of 40 to 95%, more preferably 50 to 90% of the calculated t. If it is less than 40%, it is difficult to obtain the desired pixel width.
次に実施例及び比較例を示す。Next, examples and comparative examples will be shown.
実施例1
ニッケル製ベルトの表面に金メッキした基体上に下記の
ようにして調製した着色ゲル状物質を熱融解して塗布し
た.
ポリビニルアルコール溶液( A. )の調製ポリビニ
ルアルコール
(和光純薬社製:平均重合度約1500) 5重量
%純 水 残量上記の
組成物を60℃で加温し、攪拌溶解し、放冷後、10μ
園のテフロンフィルターで濾過し、ボリビニルアルコー
ル水溶液(A)を調製した。Example 1 A colored gel-like substance prepared as described below was applied by thermal melting onto a gold-plated substrate on the surface of a nickel belt. Preparation of polyvinyl alcohol solution (A.) Polyvinyl alcohol (manufactured by Wako Pure Chemical Industries, Ltd.: average degree of polymerization approximately 1500) 5% by weight Pure water Remaining amount The above composition was heated at 60°C, dissolved with stirring, and left to cool. , 10μ
The solution was filtered using a Teflon filter manufactured by the company, and an aqueous solution of vorivinyl alcohol (A) was prepared.
顔料分散液(B)の調製
カーボンブラック(平均粒径約0.5μ隘)10重量%
エチレングリコール 40重量%f
il酸(和光純薬社製) 2重量%
純水 残量
上記組成でボールミルで20時間分散し、遠心分離器に
て粗大粒子を除き10μmテフロンフィルターで濾別し
,顔料分散液(B)を作製した。Preparation of pigment dispersion (B) Carbon black (average particle size approximately 0.5μ) 10% by weight
Ethylene glycol 40% by weight
Ilic acid (manufactured by Wako Pure Chemical Industries) 2% by weight
Pure water Remaining amount The above composition was dispersed in a ball mill for 20 hours, coarse particles were removed in a centrifuge, and filtered through a 10 μm Teflon filter to prepare a pigment dispersion (B).
(A)液を60℃で加温攪拌しながら(B)液を加え、
放冷し、ゲル状物質を得た。得られたゲルを、水洗を繰
り返し、吸引濾過し、濾液が濁らなくなるまで繰り返し
、十分に過剰の溶媒を除去し,て非流動性の黒色ゲル状
インクを得た。While heating the solution (A) at 60°C and stirring, add the solution (B),
The mixture was allowed to cool to obtain a gel-like substance. The resulting gel was repeatedly washed with water and filtered with suction until the filtrate was no longer cloudy, and the excess solvent was sufficiently removed to obtain a non-flowable black gel-like ink.
一方、ポリカーボネートフィルムにフォ[・レジスト・
層を厚みが約60μ扉になるように塗布した後5ス1−
ライブ状のパターン露光をし、エツチンヅを行なって、
メ、トライブ状のンオトレジス1・・ベターンを得た、
.:のフィル%A K真空蒸着によりフォトレジスト面
に、厚みが約50μmになるように金の膜を設けた。剥
離法によりフォトレジスト層をポリカーボネートフイル
ムから剥ぎとり、ポリカーボネートフィルムー』二に金
のストライブパターンを得た。ポリテトラフルエ口エチ
レン板(厚み1.5mm)と上記ポリカーボネートフィ
ルムとを金パターンがポリテトラフルオ口エチレン側に
重なるように接合、熱圧着した後ポリカーボネートを塩
化メチレンで溶解除去してポリテトラフルエ口エチレン
とに金のストライプパターンを得た。このポリテトラフ
ルオロエチレン板(厚み1.5ram)と他のポリテト
ラフルエ口エチレン板とを重ね合せ冫一後熱圧着し、長
さ8■に切断し、端面を研磨して第:3図に示したよう
な電極を得た。On the other hand, polycarbonate film is coated with photoresist.
After applying the layer so that the thickness is about 60 μm, 5 steps 1-
Perform live pattern exposure, perform etching,
I got a tribe-like NOTREGIS 1...Betaan.
.. A gold film was provided on the photoresist surface by vacuum evaporation to a thickness of about 50 μm. The photoresist layer was peeled off from the polycarbonate film by a peeling method to obtain a gold stripe pattern on the polycarbonate film. A polytetrafluene ethylene plate (thickness 1.5 mm) and the above polycarbonate film were bonded together so that the gold pattern overlapped with the polytetrafluene ethylene side, and after thermocompression bonding, the polycarbonate was dissolved and removed with methylene chloride to form a polytetrafluene ethylene plate. A gold stripe pattern was obtained with ethylene. This polytetrafluoroethylene plate (thickness: 1.5 ram) and another polytetrafluoroethylene plate were stacked together, heat-pressed and then cut into lengths of 8 cm, and the end surfaces were polished and shown in Figure 3. An electrode as shown was obtained.
上記のゲル層保持ベルトと電極とを第〕−図の装置に取
りつけて印字を行なった。ベルトの外周速は20iim
/seeになるように設定した。Printing was carried out by attaching the above gel layer holding belt and electrode to the apparatus shown in FIG. The outer peripheral speed of the belt is 20iim
/see.
印字には20V、3 . 5msecの矩形波パルスを
用いた。得られた画像(画素)の尾引きは極くわずかで
あった。20V for printing, 3. A 5 msec square wave pulse was used. The resulting image (pixel) had very little trailing.
比較例1
第3図のような電極を保持部材をガラスで作製して実施
例lと同様に印字したところ画像の尾引きが著しかった
.
実施例2
厚み約100 itの金の板と厚み約1″0μmのポリ
、イミドフィルムとをエボキシ系接着剤で、それぞれが
200層ずっとなるように重ね合せて接着し,約22u
++幅の電極素材を得た.この素材を切断して互いに接
着することにより110mm幅で1000個の導電体を
有する電極を得た.この電極を第5図のように先端近傍
が30℃となるように切削し、更に先端を研磨により曲
率半径約50μ罠どなるように仕上げた。この電極を第
1図の印字装置に先端部が約Sμ員ゲル層を押し下げる
ような位置に取り付けて、30V、4 . 2rase
cの矩形波パルスで印字を行なったところ、画像上の尾
引きはわずかであった。Comparative Example 1 When an electrode as shown in Figure 3 was printed in the same manner as in Example 1 using a holding member made of glass, the image had significant trailing. Example 2 A gold plate with a thickness of about 100 IT and a polyimide film with a thickness of about 1"0 μm were bonded together using an epoxy adhesive so that each layer had 200 layers.
An electrode material with a width of ++ was obtained. By cutting this material and gluing it together, electrodes with a width of 110 mm and 1000 conductors were obtained. This electrode was cut so that the temperature near the tip was 30° C. as shown in FIG. 5, and the tip was polished to a radius of curvature of about 50 μm. This electrode was attached to the printing device shown in FIG. 1 at a position such that the tip pushed down the approximately Sμ gel layer, and the voltage was set at 30V and 4.5V. 2rase
When printing was performed using a rectangular wave pulse of c, there was only slight trailing on the image.
実施例3
比較例1の電極を用いて、第1図の装置を用いて印字を
行なった。電極とゲル層との接蝕幅は約50μ腫であり
、125μIII幅の画素を得るために計算されるパル
ス幅は周速度20+++m八c(のときには3.75m
secである.この条件でパルス幅を変えて最適条件を
探した結果約3 . 3IIlsecで最も尾引きが少
なく、所望の画素幅が得られた。Example 3 Using the electrode of Comparative Example 1, printing was performed using the apparatus shown in FIG. The etching width between the electrode and the gel layer is approximately 50 μm, and the pulse width calculated to obtain a pixel with a width of 125 μIII is 3.75 m when the circumferential speed is 20 + + + m8c (
sec. We searched for the optimal conditions by changing the pulse width under these conditions, and the result was approximately 3. The desired pixel width was obtained with the least tailing at 3IIlsec.
更に、周速を5 〜100mm+/seeで変化し,て
,入力パルス電圧、パルス幅を変えて同様に最適パルス
印加時間を探したところ、周速を大きくしてパルス電圧
を高くした時には,計算値に対して虹に短い時間だけパ
ルスを印加した時に良好な画像が得られることが判明し
た。結果として計算時間に対して40〜95%の時間だ
けパルスを印加するときに尾引きがなく所望の画素幅が
得られた。Furthermore, when the circumferential speed was varied from 5 to 100 mm+/see, and the input pulse voltage and pulse width were changed, the optimum pulse application time was similarly searched, and when the circumferential speed was increased and the pulse voltage was increased, the calculation It has been found that good images can be obtained when the rainbow is pulsed for a short period of time. As a result, the desired pixel width was obtained without tailing when the pulse was applied for 40 to 95% of the calculation time.
本発明によれば下記のような効果がもたらされる。 According to the present invention, the following effects are brought about.
(1)電極に流動化したインクが付着し、パルス電圧を
印加した後にも流動化したインクが流動化していないイ
ンクの表面に付着してきたとしても、その分だけパルス
の印加時間が短かくなっているため、尾引きを生じるこ
とがなく、所望の画素幅を得ることが出来る.
(2)第3図、第4図に示したような導電体のに接して
、低表面エネルギーの部材があるので,流動化したイン
クは導電体の部分にしか付着しないため、流動化してい
ないゲル層によう容易にクリーニングされるため,画像
の尾引きが著しく少なくなる.
(3)第5図、第6図、第7図に示したように、電極の
ゲル層に接する部分が鋭角となっているため、流動性し
たインクによって濡らされる電極部分が少なくなるため
、余分に付着するインク量も少なくなり、この場合も流
動化していないゲル層により容易にクリーニングされる
ため、画像の尾引きが著しく少なくなる.
(4)上記の(1)(2)及び(3)はそれぞれ単独に
用いても効果があるが、これらの全部又は二つを組合せ
ることにより更に効果のあがることが認められる。また
、第1図においてはゲル層から直接記録紙に転写する例
を示したが、中間転写体に一度転写した後に中間転写体
から記録紙に転写するような装置構成としたとしても、
本発明が同様に効果を有することは明らかである。(1) Even if the fluidized ink adheres to the electrode and the fluidized ink adheres to the surface of the unfluidized ink even after the pulse voltage is applied, the pulse application time will be shortened accordingly. Therefore, the desired pixel width can be obtained without causing trailing. (2) As there is a member with low surface energy in contact with the conductor as shown in Figures 3 and 4, the fluidized ink only adheres to the conductor, so it is not fluidized. Because the gel layer is easily cleaned, trailing in images is significantly reduced. (3) As shown in Figures 5, 6, and 7, since the part of the electrode that contacts the gel layer is at an acute angle, the part of the electrode that is wetted by fluid ink is reduced, resulting in excess The amount of ink adhering to the ink is also reduced, and in this case too, it is easily cleaned by the unfluidized gel layer, so the trailing of the image is significantly reduced. (4) The above (1), (2) and (3) are effective even when used alone, but it is recognized that the effect is further increased by combining all or two of them. Further, although FIG. 1 shows an example in which the gel layer is directly transferred to the recording paper, even if the apparatus is configured such that the gel layer is transferred once to the intermediate transfer body and then transferred from the intermediate transfer body to the recording paper,
It is clear that the invention has similar advantages.
第1図は本発明装置の代表的な一例の概略図である.第
2図から第7図までは電極の複数例を表わした図である
。第8図は所望の画素幅を得るための説明図である。
2・・・記録紙 3・・・ヒーター5・・
・ゲル状層保持ベルト 6・・・電極+1a,8b・・
・基体移動ローラ
IO・・・インク塗布ローラ l2・・・基体ベルト
13・・・インク層(着色ゲル状物質M)第4図
第8図FIG. 1 is a schematic diagram of a typical example of the device of the present invention. FIG. 2 to FIG. 7 are diagrams showing a plurality of examples of electrodes. FIG. 8 is an explanatory diagram for obtaining a desired pixel width. 2... Recording paper 3... Heater 5...
・Gel layer holding belt 6... Electrodes +1a, 8b...
・Substrate moving roller IO... Ink application roller l2... Base belt 13... Ink layer (colored gel-like substance M) Fig. 4 Fig. 8
Claims (1)
ル状物質層を設け、そのゲル状物質層に画像信号に従っ
て電極により通電した後、通電後の流動性となった着色
物質を選択的に被転写媒体に転写せしめる画像記録装置
において、前記電極の少なくとも片面に臨界表面張力3
5dyne/cm(20℃)以下の材料を接合せしめた
ことを特徴とする画像記録装置。 2、基体表面に着色剤を含み通電により流動性となるゲ
ル状物質層を設け、そのゲル状物質層に画像信号に従っ
て電極により通電した後、通電後の流動性となった着色
物質を選択的に被転写媒体に転写せしめる画像記録装置
において、前記電極のゲル状物質層に接する部分の近傍
を鋭角にしたことを特徴とする画像記録装置。 3、基体表面に着色剤を含み通電により流動性となるゲ
ル状物質層を設け、そのゲル状物質に画像信号に従って
電極により通電した後、通電後の流動性となった着色物
質を選択的に被転写媒体に転写せしめる画像記録方法に
おいて、前記の基体と電極とを相対的に移動せしめて通
電を行なう際に、一画素を形成する為に、基体表面のゲ
ル状物質層外周が連続的に周速vで移動され、電極とゲ
ル状物質層との接触幅が送り方向にwであり、目標とす
る送り方向の画素幅をwとしたとき、式 ▲数式、化学式、表等があります▼ により導かれるtの値の40〜95%になるだけの時間
通電することを特徴とする画像記録方法。[Claims] 1. A gel-like material layer containing a colorant that becomes fluid when energized is provided on the surface of the substrate, and after electricity is applied to the gel-like material layer using an electrode according to an image signal, the fluidity becomes fluid after energization. In an image recording apparatus that selectively transfers a colored substance to a transfer medium, at least one surface of the electrode has a critical surface tension of 3.
An image recording device characterized by bonding materials of 5 dyne/cm (20°C) or less. 2. A gel-like material layer containing a colorant that becomes fluid when energized is provided on the surface of the substrate, and after energizing the gel-like material layer with an electrode according to an image signal, the colored material that has become fluid after energization is selectively removed. What is claimed is: 1. An image recording device for transferring an image to a transfer medium, characterized in that a portion of the electrode in contact with a gel-like material layer has an acute angle. 3. A layer of gel-like material containing a colorant that becomes fluid when energized is provided on the surface of the substrate, and after energizing the gel-like material with an electrode according to an image signal, the colored material that has become fluid after energization is selectively removed. In an image recording method for transferring an image to a transfer medium, when the substrate and the electrode are relatively moved and energized, the outer periphery of the gel-like material layer on the surface of the substrate is continuously formed to form one pixel. When it is moved at a circumferential speed v, the contact width between the electrode and the gel material layer is w in the feeding direction, and the target pixel width in the feeding direction is w, there are formulas ▲ mathematical formulas, chemical formulas, tables, etc. ▼ An image recording method characterized in that electricity is applied for a time that is 40 to 95% of the value of t derived by .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1057455A JP2771832B2 (en) | 1989-03-08 | 1989-03-08 | Image recording method and apparatus |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1057455A JP2771832B2 (en) | 1989-03-08 | 1989-03-08 | Image recording method and apparatus |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02235653A true JPH02235653A (en) | 1990-09-18 |
JP2771832B2 JP2771832B2 (en) | 1998-07-02 |
Family
ID=13056143
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Application Number | Title | Priority Date | Filing Date |
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JP1057455A Expired - Fee Related JP2771832B2 (en) | 1989-03-08 | 1989-03-08 | Image recording method and apparatus |
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Country | Link |
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JP (1) | JP2771832B2 (en) |
-
1989
- 1989-03-08 JP JP1057455A patent/JP2771832B2/en not_active Expired - Fee Related
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