JPH01146789A - Heating body - Google Patents
Heating bodyInfo
- Publication number
- JPH01146789A JPH01146789A JP62304805A JP30480587A JPH01146789A JP H01146789 A JPH01146789 A JP H01146789A JP 62304805 A JP62304805 A JP 62304805A JP 30480587 A JP30480587 A JP 30480587A JP H01146789 A JPH01146789 A JP H01146789A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- resistant layer
- heating
- heating element
- layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000010438 heat treatment Methods 0.000 title claims abstract description 100
- 229920005989 resin Polymers 0.000 claims abstract description 32
- 239000011347 resin Substances 0.000 claims abstract description 32
- 239000000654 additive Substances 0.000 claims abstract description 29
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 23
- 230000000996 additive effect Effects 0.000 claims abstract description 21
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 11
- 239000004094 surface-active agent Substances 0.000 claims abstract description 11
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 7
- 239000011737 fluorine Substances 0.000 claims abstract description 7
- 150000001408 amides Chemical class 0.000 claims abstract description 6
- 239000002245 particle Substances 0.000 claims description 6
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 5
- 239000006082 mold release agent Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 abstract description 23
- 238000000034 method Methods 0.000 abstract description 7
- 230000001050 lubricating effect Effects 0.000 abstract description 5
- 238000000926 separation method Methods 0.000 abstract description 4
- 238000012643 polycondensation polymerization Methods 0.000 abstract description 2
- 238000010526 radical polymerization reaction Methods 0.000 abstract description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 24
- 239000011248 coating agent Substances 0.000 description 23
- 239000003973 paint Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- -1 perfluoroalkyl sulfonates Chemical class 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000000118 dimethyl group Polymers [H]C([H])([H])* 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- UXHQLGLGLZKHTC-CUNXSJBXSA-N 4-[(3s,3ar)-3-cyclopentyl-7-(4-hydroxypiperidine-1-carbonyl)-3,3a,4,5-tetrahydropyrazolo[3,4-f]quinolin-2-yl]-2-chlorobenzonitrile Chemical compound C1CC(O)CCN1C(=O)C1=CC=C(C=2[C@@H]([C@H](C3CCCC3)N(N=2)C=2C=C(Cl)C(C#N)=CC=2)CC2)C2=N1 UXHQLGLGLZKHTC-CUNXSJBXSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 2
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 2
- BIIBYWQGRFWQKM-JVVROLKMSA-N (2S)-N-[4-(cyclopropylamino)-3,4-dioxo-1-[(3S)-2-oxopyrrolidin-3-yl]butan-2-yl]-2-[[(E)-3-(2,4-dichlorophenyl)prop-2-enoyl]amino]-4,4-dimethylpentanamide Chemical compound CC(C)(C)C[C@@H](C(NC(C[C@H](CCN1)C1=O)C(C(NC1CC1)=O)=O)=O)NC(/C=C/C(C=CC(Cl)=C1)=C1Cl)=O BIIBYWQGRFWQKM-JVVROLKMSA-N 0.000 description 1
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- DWKNOLCXIFYNFV-HSZRJFAPSA-N 2-[[(2r)-1-[1-[(4-chloro-3-methylphenyl)methyl]piperidin-4-yl]-5-oxopyrrolidine-2-carbonyl]amino]-n,n,6-trimethylpyridine-4-carboxamide Chemical compound CN(C)C(=O)C1=CC(C)=NC(NC(=O)[C@@H]2N(C(=O)CC2)C2CCN(CC=3C=C(C)C(Cl)=CC=3)CC2)=C1 DWKNOLCXIFYNFV-HSZRJFAPSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- SJVGFKBLUYAEOK-SFHVURJKSA-N 6-[4-[(3S)-3-(3,5-difluorophenyl)-3,4-dihydropyrazole-2-carbonyl]piperidin-1-yl]pyrimidine-4-carbonitrile Chemical compound FC=1C=C(C=C(C=1)F)[C@@H]1CC=NN1C(=O)C1CCN(CC1)C1=CC(=NC=N1)C#N SJVGFKBLUYAEOK-SFHVURJKSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- MWHHJYUHCZWSLS-UHFFFAOYSA-N FC=1C=C(C=CC1C1=C2CNC(C2=C(C=C1)C=1NC(=CN1)C)=O)NC(=O)NC1=C(C=C(C=C1F)F)F Chemical compound FC=1C=C(C=CC1C1=C2CNC(C2=C(C=C1)C=1NC(=CN1)C)=O)NC(=O)NC1=C(C=C(C=C1F)F)F MWHHJYUHCZWSLS-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- MCRWZBYTLVCCJJ-DKALBXGISA-N [(1s,3r)-3-[[(3s,4s)-3-methoxyoxan-4-yl]amino]-1-propan-2-ylcyclopentyl]-[(1s,4s)-5-[6-(trifluoromethyl)pyrimidin-4-yl]-2,5-diazabicyclo[2.2.1]heptan-2-yl]methanone Chemical compound C([C@]1(N(C[C@]2([H])C1)C(=O)[C@@]1(C[C@@H](CC1)N[C@@H]1[C@@H](COCC1)OC)C(C)C)[H])N2C1=CC(C(F)(F)F)=NC=N1 MCRWZBYTLVCCJJ-DKALBXGISA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical class OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- UXZAJSZFFARTEI-GUMHCPJTSA-N methyl (2R,3S)-3-(methanesulfonamido)-2-[(4-phenylcyclohexyl)oxymethyl]piperidine-1-carboxylate Chemical compound COC(=O)N1CCC[C@H](NS(C)(=O)=O)[C@@H]1COC1CCC(CC1)c1ccccc1 UXZAJSZFFARTEI-GUMHCPJTSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/423—Intermediate, backcoat, or covering layers characterised by non-macromolecular compounds, e.g. waxes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/44—Intermediate, backcoat, or covering layers characterised by the macromolecular compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/44—Intermediate, backcoat, or covering layers characterised by the macromolecular compounds
- B41M5/443—Silicon-containing polymers, e.g. silicones, siloxanes
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、例えば、高速・低電力で画像もしくは文字を
記録する通電感熱転写記録に用いられる発熱体、特に安
定で高画質の画像もしくは文字を低価格で提供する通電
感熱転写記録に適した発熱体に関する。 ・
従来の技術
感熱転写記録方式は、サーマルヘッドを用いて記録を行
っていたが、サーマルヘッドの蓄熱が大きいため高速記
録をし難い問題点があった。この間面皮に対して、例え
ば米国特許第3. 744゜611号明細書に記載され
ているように、分離電極と帰還電極とを有する通電ヘッ
ドと、発熱抵抗層と熱溶融インク廖が一体となった通電
転写リボンと、記録紙を用い記録する通電感熱記録技術
が提案された。しかしこの提案では、通電転写リボンが
高価であるため、ランニングコストが高くつく欠点を有
していた。この欠点に対して、例えば特開昭61−17
9764号公報、特開昭61−199996号公報に記
載されているように、通電ヘッドと、発熱シートと、熱
溶融転写シートと、記録紙とを用い、発熱シートを複数
回使用することによってランニングコストの低減を行う
提案がされている。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to heating elements used, for example, in electrical thermal transfer recording for recording images or characters at high speed and low power, and in particular for recording stable, high-quality images or characters at low power consumption. This invention relates to a heating element suitable for electric thermal transfer recording that is available at a reasonable price. - Conventional technology Thermal transfer recording method uses a thermal head to perform recording, but there is a problem in that it is difficult to perform high-speed recording because the thermal head accumulates a large amount of heat. During this period, for example, US Pat. As described in the specification of No. 744゜611, recording is performed using a current-carrying head having a separation electrode and a return electrode, a current-carrying transfer ribbon in which a heat-generating resistive layer and a heat-melting ink cartridge are integrated, and a recording paper. Electrical thermal recording technology was proposed. However, this proposal has the drawback of high running costs because the electrically conductive transfer ribbon is expensive. For this drawback, for example, Japanese Patent Laid-Open No. 61-17
As described in Japanese Patent Laid-open No. 9764 and Japanese Patent Application Laid-open No. 199996/1989, running is performed by using a current-carrying head, a heat-generating sheet, a heat-melting transfer sheet, and a recording paper, and using the heat-generating sheet multiple times. Proposals have been made to reduce costs.
発明が解決しようとする問題点
上記の提案はいずれも通電ヘッドに記録信号電流を供給
しながら通電ヘッドが発熱シート上を摺動するため、通
電ヘッドの電極部(分離電極と帰還型gりと発熱シート
との間の電気的接触を恒常的に保つことが困難という欠
点があった。Problems to be Solved by the Invention In all of the above proposals, since the current-carrying head slides on a heat-generating sheet while supplying a recording signal current to the current-carrying head, the electrode part of the current-carrying head (separated electrode and feedback type g) is There was a drawback that it was difficult to permanently maintain electrical contact with the heat generating sheet.
そこで通電ヘッドと、発熱抵抗層上に滑性耐熱層を具備
した発熱部材と、記録材料とからなり、記録信号電流の
供給時には通電ヘッドと発熱部材との相対位置を固定し
、発熱部材と記録材料間で摺動させて記録する記録方法
が上記欠点を克服できる記録方法である。Therefore, it consists of a current-carrying head, a heat-generating member having a slippery heat-resistant layer on a heat-generating resistive layer, and a recording material. A recording method in which recording is performed by sliding between materials is a recording method that can overcome the above-mentioned drawbacks.
本発明の目的は、記録材料を安定にしかも長時間摺動さ
せる発熱体を提供することにある。An object of the present invention is to provide a heating element that allows a recording material to slide stably and for a long time.
問題点を解決するための手段
発熱抵抗層上に滑性耐熱層を具備し、前記滑性耐熱層が
弗素系、シリコーン系、もしくは酸アマイド系の離型剤
か界面活性剤の内少なくとも1種類の添加剤と熱硬化性
樹脂とを含む。Means for Solving the Problems A slippery heat-resistant layer is provided on the heat-generating resistive layer, and the slippery heat-resistant layer is made of at least one type of fluorine-based, silicone-based, or acid amide-based mold release agent or surfactant. additives and a thermosetting resin.
作用
滑性耐熱層の熱硬化性樹脂が、発熱抵抗体の発熱に体し
て耐熱性を発揮する。滑性耐熱層の弗素系、シリコーン
系もしくは酸アマイド系の雌型剤か界面活性剤の内少な
くとも1種類の添加剤が、記録材料と発熱体との摩擦係
数を低下させる。上記2点により、記録材料を安定にし
かも長時間摺動する発熱体を提供することができる。The thermosetting resin of the slippery heat-resistant layer exhibits heat resistance against the heat generated by the heating resistor. At least one type of additive among fluorine-based, silicone-based, or acid amide-based female agents or surfactants in the slippery heat-resistant layer lowers the coefficient of friction between the recording material and the heating element. Due to the above two points, it is possible to provide a heating element that can stably slide a recording material over a long period of time.
実施例
第4図に1本発明の発熱体を用いた記録方法の1実施態
様の概念構成断面図を示す。Embodiment FIG. 4 is a conceptual cross-sectional view of an embodiment of a recording method using a heating element of the present invention.
分離電極lと帰還電極2とを有する通電ヘッド3と、発
熱抵抗層4上に滑性耐熱層5を有する発熱体6と、感熱
記録材料7、プラテン8とから構成されている。先ず電
源9から記録信号が分M電極1を通り、発熱抵抗層4を
経て、帰i1電極2に帰還する。発熱抵抗M4に記録信
号電流が流れると、発熱抵抗N4が発熱し、この熱によ
って感熱記録材料7に記録される。感熱記録材料7は、
直接熱によって発色する感熱紙でも、また熱転写シート
と記録紙でも良い。熱転写シートを用いる場合は、転写
シートのインク面と異なる面を滑性耐熱層5側にするこ
と勿論である。It is composed of a current-carrying head 3 having a separation electrode 1 and a return electrode 2, a heating element 6 having a slippery heat-resistant layer 5 on a heating resistance layer 4, a heat-sensitive recording material 7, and a platen 8. First, a recording signal from the power source 9 passes through the minute electrode 1, passes through the heating resistor layer 4, and returns to the return electrode 2. When a recording signal current flows through the heat generating resistor M4, the heat generating resistor N4 generates heat, and this heat is used to record on the thermosensitive recording material 7. The heat-sensitive recording material 7 is
It may be thermal paper that develops color by direct heat, or a thermal transfer sheet and recording paper. When using a thermal transfer sheet, it goes without saying that the surface of the transfer sheet that is different from the ink surface should face the slippery heat-resistant layer 5 side.
本発明の発熱抵抗層4は、例えばポリイミド。The heat generating resistance layer 4 of the present invention is made of polyimide, for example.
ポリアミド等の耐熱性樹脂とカーボン等の導電性粒子と
を練り込んで抵抗値を制御した物や、例えばCr、Ta
N、TiC−5i02.Cr−3iO2、T 1C−S
iC,Ti、−AI−N等をスパッタあるいは真空蒸
着法等によって膜厚を制御した物等が挙げられる。Products whose resistance value is controlled by mixing heat-resistant resin such as polyamide with conductive particles such as carbon, etc.
N, TiC-5i02. Cr-3iO2, T1C-S
Examples include those in which iC, Ti, -AI-N, etc. are controlled in film thickness by sputtering or vacuum evaporation.
滑性耐熱層5は、感熱記録材料7を摺動させる滑性と、
発熱抵抗層4で発熱した熱に対する耐熱性と、発熱抵抗
層4で発熱した熱を感熱記録材料7へ伝える熱伝導性が
必要である。The lubricious heat-resistant layer 5 has lubricity that allows the heat-sensitive recording material 7 to slide;
It is necessary to have heat resistance to the heat generated by the heat generating resistor layer 4 and thermal conductivity to transfer the heat generated by the heat generating resistor layer 4 to the thermosensitive recording material 7.
本発明の発熱体を用いると、記録信号が通電ヘッド3に
印加されている間は少なくとも通電ヘッド3と発熱体6
との相対位置を変化させずに記録でき、記録信号が通電
ヘッド3に印加されていない時通電ヘッド3と発熱体6
との相対位置を変化させることができる。従って従来の
欠点であった電気的接触不良が起こらない通電感熱記録
が可能である。また熱効率が良く、サーマルヘッドの約
1/2の記録エネルギで、5倍以上の高速記録が可能で
ある。更に通電へラド3と発熱体6は、従来のサーマル
ヘッドより安価である。When the heating element of the present invention is used, while a recording signal is being applied to the energizing head 3, at least the energizing head 3 and the heating element 6
When the recording signal is not applied to the current-carrying head 3, the current-carrying head 3 and the heating element 6 can record without changing their relative position.
You can change the relative position with. Therefore, it is possible to carry out current-conducting heat-sensitive recording without causing electrical contact failure, which is a drawback of the conventional method. It also has good thermal efficiency and can record at least five times faster with about half the recording energy of a thermal head. Furthermore, the energizing head 3 and heating element 6 are cheaper than conventional thermal heads.
第1図に本発明の発熱体の1実施態様の概念構成断面図
を示す。発熱抵抗N4上に、添加剤と熱硬化性樹脂とを
含む滑性耐熱N5が形成されている。FIG. 1 shows a conceptual cross-sectional view of one embodiment of the heating element of the present invention. A slippery heat-resistant layer N5 containing an additive and a thermosetting resin is formed on the heat-generating resistor N4.
熱硬化性樹脂は、一般にラジカル重合もしくはイオン重
合によって硬化する樹脂か、もしくは縮合重合で硬化す
る樹脂であり、例えはエポキシアクリレート、ウレタン
アクリレート、ポリエステルアクリレート等のアクリレ
ート類、フェノール樹脂、ユリア樹脂、メラミン樹脂、
不飽和ポリエステル樹脂、エポキシ樹脂等が挙げられる
。これらの樹脂は、その反応形態に応して増感剤、硬化
促進剤9反応性希釈剤等を混入しても良い・添加剤は、
熱硬化性樹脂中に含ますことにより、滑性耐熱N5と感
熱記録材料7との摩擦係数を減らし感熱記録材料を摺動
しやすくする。添加剤の村村としてはジメチルポリシロ
キサン、アルキルアリル変性等のシリコーンオイル、ジ
メチルシリコーンのポリエーテル変性、ジメチルシリコ
ーンのカルボキシ変性、ジメチルシリコーンのアミド変
性等のシリコーン界面活性剤、パーフルオロアルキルス
ルホン酸塩、パーフルオロアルキルカルボン酸塩、パー
フルオロアルキルエチレンオキシド付加物、パーフルオ
ロアルキル基・親水性基・親油性基含有オリゴマー、パ
ーフルオロアリキル基・親油性基含有ウレタン、パーフ
ルオロアルキル燐酸エステル等の弗素系界面活性剤、脂
肪酸アマイド等が挙げられ、これらの添加剤は単一もし
くは2種以上複合して用いられる。Thermosetting resins are generally resins that are cured by radical polymerization or ionic polymerization, or resins that are cured by condensation polymerization, such as acrylates such as epoxy acrylates, urethane acrylates, and polyester acrylates, phenolic resins, urea resins, and melamine. resin,
Examples include unsaturated polyester resins and epoxy resins. These resins may be mixed with sensitizers, curing accelerators, 9 reactive diluents, etc. depending on the reaction form.Additives include:
By including it in the thermosetting resin, the coefficient of friction between the slippery heat-resistant N5 and the heat-sensitive recording material 7 is reduced, making it easier for the heat-sensitive recording material to slide. Muramura's additives include silicone oils such as dimethylpolysiloxane and alkylaryl-modified silicone oils, silicone surfactants such as polyether-modified dimethyl silicone, carboxy-modified dimethyl silicone, and amide-modified dimethyl silicone, and perfluoroalkyl sulfonates. , perfluoroalkyl carboxylic acid salts, perfluoroalkyl ethylene oxide adducts, oligomers containing perfluoroalkyl groups/hydrophilic groups/lipophilic groups, urethanes containing perfluoroalkyl groups/lipophilic groups, perfluoroalkyl phosphate esters, etc. Examples include surfactants, fatty acid amides, and the like, and these additives may be used singly or in combination of two or more.
添加剤の含有量は、熱硬化性樹脂のO81〜10重量%
の範囲が好ましい。添加剤が熱硬化性樹脂11の0.
1重量%未溝であると、不均一な摩擦係数となる場合が
ある。また添加剤が熱硬化性樹脂の10重量%より多い
と、熱硬化性樹脂及び添加剤各々の材料によっては発熱
抵抗N4との密着力が低下する場合がある。The content of the additive is O81 to 10% by weight of the thermosetting resin.
A range of is preferred. The additive is 0.0% of the thermosetting resin 11.
If 1% by weight of the groove is ungrooved, the coefficient of friction may be uneven. Furthermore, if the amount of the additive is more than 10% by weight of the thermosetting resin, the adhesion to the heating resistor N4 may decrease depending on the materials of the thermosetting resin and the additive.
滑性耐熱N5は、添加剤以外に粒子を含有していても良
い。粒子の材料としては、例えば酸化珪素、弗化炭素、
タルク、メラミン樹脂、グアナミン樹脂、アルミナ、窒
化硼素、窒化珪素、珪酸アルミニウム、炭酸カルシウム
、珪酸カルシウム。The slippery heat-resistant N5 may contain particles in addition to additives. Examples of particle materials include silicon oxide, carbon fluoride,
Talc, melamine resin, guanamine resin, alumina, boron nitride, silicon nitride, aluminum silicate, calcium carbonate, calcium silicate.
酸化チタン、水酸化アルミニウム、硫酸バリウム等が挙
げられる。Examples include titanium oxide, aluminum hydroxide, barium sulfate, and the like.
滑性耐熱層5の厚みは、熱伝導性に強く影響を与え、厚
みが薄いほど熱伝導性が良好となるが、耐熱性は劣る。The thickness of the slippery heat-resistant layer 5 has a strong influence on thermal conductivity, and the thinner the thickness, the better the thermal conductivity, but the worse the heat resistance.
従って滑性耐熱層5の厚みは、1〜10μmが好ましい
。Therefore, the thickness of the slippery heat-resistant layer 5 is preferably 1 to 10 μm.
滑性耐熱層5の塗工方法は、例えばバーコータ。The coating method for the slippery heat-resistant layer 5 is, for example, a bar coater.
グラビアコータ、リバースコータ等通常の手法で塗工て
きる。また通常熱硬化性樹脂は、塗工後硬化反応を行う
。Coating can be done using conventional methods such as gravure coater or reverse coater. Further, thermosetting resins usually undergo a curing reaction after being applied.
第2図に本発明の他の実施態様の概念構成断面図を示す
。発熱抵抗層4と滑性耐熱層5との界面に電極NIOが
形成されている。FIG. 2 shows a conceptual cross-sectional view of another embodiment of the present invention. An electrode NIO is formed at the interface between the heat generating resistance layer 4 and the slippery heat resistant layer 5.
第3図に本発明の別の実施態様の概念構成断面図を示す
。発熱抵抗N4が通電高抵抗Nll上に積層されていて
、滑性耐熱N5が発熱抵抗層4−ヒに形成されている。FIG. 3 shows a conceptual structural sectional view of another embodiment of the present invention. A heat generating resistor N4 is laminated on the current-carrying high resistance Nll, and a slippery heat resistant layer N5 is formed on the heat generating resistor layer 4-H.
第1図〜第3図に示した滑性耐熱層5は、通常シート状
てあり、記録信号が印加されていない時、通電ヘッド3
との相対位置をずらせる。The slippery heat-resistant layer 5 shown in FIGS. 1 to 3 is usually in the form of a sheet, and when no recording signal is applied, the lubricious heat-resistant layer 5 is
shift the relative position.
以下具体的な実施例を説明する。Specific examples will be described below.
実施例−1
O発熱抵抗層
カーボン含有の芳香族ポリアミドフィルム(シート抵抗
層I KΩ/口)を用いた。Example-1 O heating resistance layer A carbon-containing aromatic polyamide film (sheet resistance layer I KΩ/hole) was used.
○滑性耐熱層 まず以下の組成の塗液を用意した。○Smooth heat-resistant layer First, a coating liquid with the following composition was prepared.
熱硬化1樹脂:エポキシアクリレート5PI509(昭
和高分子■製以下同じ)
30重量部
増感剤:ダロキュア−1173(メルク社製以下同じ)
1.5重量部
添加剤:シリコーンオイルL−45(100)(日本ユ
ニカー−製) 3重量部溶媒:酢酸エチル
70重量部上記組成の塗料を溶解して、上記
発熱抵抗層上に、バーコータで塗工し、溶媒を乾燥させ
た後lKWの高圧水銀灯を2分間照射して硬化させて発
熱体1を得た。塗工厚みは371mであった。Thermosetting 1 resin: Epoxy acrylate 5PI509 (manufactured by Showa Kobunshi ■) 30 parts by weight Sensitizer: Darocure-1173 (manufactured by Merck & Co., Ltd.)
1.5 parts by weight Additive: Silicone oil L-45 (100) (manufactured by Nippon Unicar) 3 parts by weight Solvent: ethyl acetate
70 parts by weight of the paint having the above composition was dissolved and applied onto the heat generating resistor layer using a bar coater. After drying the solvent, it was cured by irradiating it with a 1KW high pressure mercury lamp for 2 minutes to obtain heat generating element 1. . The coating thickness was 371 m.
実施例−2
0発熱抵抗層
実施例−1のカーボン含有ポリアミドフィルムに、アル
ミニウムを600オングストロ一ム蒸着したフィルム(
シート抵抗約1Ω/口)を用いた。Example 2 0 Heating Resistance Layer A film (600 angstroms of aluminum) was deposited on the carbon-containing polyamide film of Example 1.
A sheet resistance of approximately 1Ω/mouth) was used.
O滑性耐熱層
実施例−1の塗液を実施例−1と同様の手法で塗工上硬
化させて発熱体2を得た。塗工厚みは371tnであっ
た。Heat generating element 2 was obtained by coating and curing the coating liquid of O-slip heat-resistant layer Example-1 in the same manner as in Example-1. The coating thickness was 371 tn.
実施例−3
0発熱抵抗層
カーボン含有のポリイミドフィルム(シート抵抗層2に
Ω/口)に、7ic−SiO2を約1000オングスト
ロームスバ・ツタで付けて(シート抵抗約200Ω/口
)発熱抵抗層とした。Example-3 0 Heating Resistance Layer 7ic-SiO2 was attached to a carbon-containing polyimide film (sheet resistance layer 2 Ω/hole) with approximately 1000 angstroms of vines (sheet resistance approximately 200 Ω/hole) to form a heating resistance layer. did.
O滑性耐熱層
実施例−1の塗液を実施例−1と同様の手法で塗工し、
硬化させて発熱体3を得た。塗工厚みは3ノtmであっ
た。O-slip heat-resistant layer The coating liquid of Example-1 was applied in the same manner as in Example-1,
The heating element 3 was obtained by curing. The coating thickness was 3 knots.
実施例−4 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-4 0 heating resistance layer The heating resistance layer of Example-3 was used.
O滑性耐熱層 まず以下の組成の塗液を用意した。O slippery heat resistant layer First, a coating liquid with the following composition was prepared.
熱硬化性樹脂:エポキシアクリレート5P1509
30重量部増感剤:ダロキュア−1
173
1、5重量部
添加剤:シリコーン界面活性剤L −7500(日本ユ
ニカー−製以下同じ) 31漬部溶媒:
70重置部り記絹成の塗料を溶解して、上
記発熱抵抗層上に、バーコータで塗工し、溶媒を乾燥さ
せた後IKWの高圧水銀灯を2分間照射して硬化させて
発熱体4を得た。塗工厚みは37zmであった。Thermosetting resin: Epoxy acrylate 5P1509
30 parts by weight Sensitizer: Darocure-1
173 1.5 parts by weight Additive: Silicone surfactant L-7500 (manufactured by Nippon Unicar) 31 parts by weight Solvent:
70 Layout Parts: Melt the Kinusei paint and apply it on the heating resistor layer using a bar coater. After drying the solvent, irradiate it with an IKW high-pressure mercury lamp for 2 minutes to harden it to form the heating element 4. I got it. The coating thickness was 37 zm.
実施例−5 Off熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-5 Off heat resistance layer The heating resistance layer of Example-3 was used.
○滑性耐熱層
実施例−4と同じ塗料を用い、同様に乾燥硬化させて発
熱体5を得た。塗工厚みは1011mであった。- Smooth heat-resistant layer Using the same paint as in Example 4, it was dried and cured in the same manner to obtain heating element 5. The coating thickness was 1011 m.
実施例−6 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-6 0 heating resistance layer The heating resistance layer of Example-3 was used.
O滑性耐熱層
実施例−4と同じ塗料を用い、同様に乾燥硬化させて発
熱体6を得た。塗工厚みは15μmであった。O Slip heat-resistant layer Using the same paint as in Example 4, it was dried and cured in the same manner to obtain a heating element 6. The coating thickness was 15 μm.
実施例−7 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-7 0 heating resistance layer The heating resistance layer of Example-3 was used.
O滑性耐熱層
゛実施例−4と同じ塗料を用い、同様に乾燥硬化
させて発熱体7を得た。塗工厚みは1.57Lmであっ
た。Heat generating element 7 was obtained by drying and curing in the same manner using the same paint as in O-lubricious heat-resistant layer (Example 4). The coating thickness was 1.57 Lm.
実施例−8 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-8 0 heating resistance layer The heating resistance layer of Example-3 was used.
○滑性耐熱層
実施例−4と同じ塗料を用い、同様に乾燥硬化させて発
熱体8を得た。塗工厚みは0゜671mであった。- Smooth heat-resistant layer Using the same paint as in Example 4, it was dried and cured in the same manner to obtain heating element 8. The coating thickness was 0°671 m.
実施例−9 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-9 0 heating resistance layer The heating resistance layer of Example-3 was used.
O滑性耐熱層
実施例−4の塗料の添加剤L−7500を0.03重量
部とした塗料を用意し、実施例−4と同様に乾燥硬化さ
せて発熱体9を得た。O Slip heat-resistant layer A paint containing 0.03 parts by weight of additive L-7500 in the paint of Example-4 was prepared and dried and cured in the same manner as in Example-4 to obtain a heating element 9.
塗工厚みは3μmであった。The coating thickness was 3 μm.
実施例−10 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-10 0 heating resistance layer The heating resistance layer of Example-3 was used.
O滑性耐熱層
実施例−4の塗料の添加剤L−7500を0.006重
量部とした塗料を用意し、実施例−4と同様に乾燥硬化
させて発熱体10を得た。塗工厚みは371mであった
。O Slip heat-resistant layer A paint containing 0.006 parts by weight of additive L-7500 in the paint of Example-4 was prepared and dried and cured in the same manner as in Example-4 to obtain a heating element 10. The coating thickness was 371 m.
実施例−11 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-11 0 heating resistance layer The heating resistance layer of Example-3 was used.
○滑性耐熱層 まず以下の組成の塗液な用、依した。○Smooth heat-resistant layer First, a coating liquid with the following composition was used.
熱硬化性樹脂:スミテックスレジンM−3(住友化学工
業■製) 100重量部硬化剤:スミテックスア
クセレレータACX(住友化学工業−!り
10重量部硬化促進剤:スミテックスアクセレレータX
−80(住友化学工業(牟1製) 2重量部溶媒:水
100重量部添加剤:弗素系界面
活性剤メガファックF−177(大日本インキ■製)
3重量部玉記絹成の塗料をボールミルで30分間分散
して、上記発熱抵抗層上に、バーコータで塗工し、溶剤
を乾燥させた後150℃で1時間加熱して硬化させて発
熱体11を得た。塗工厚みは1071mであった。Thermosetting resin: Sumitex Resin M-3 (manufactured by Sumitomo Chemical Co., Ltd.) 100 parts by weight Curing agent: Sumitex Accelerator ACX (manufactured by Sumitomo Chemical Co., Ltd.)
10 parts by weight Curing accelerator: Sumitex Accelerator
-80 (manufactured by Sumitomo Chemical Co., Ltd. (Mu1) 2 parts by weight Solvent: Water 100 parts by weight Additive: Fluorine surfactant Megafac F-177 (manufactured by Dainippon Ink ■)
3 parts by weight of Tamaki Kinsei's paint was dispersed in a ball mill for 30 minutes, coated on the heat generating resistor layer with a bar coater, dried the solvent, and heated at 150°C for 1 hour to harden to form a heat generating element. I got 11. The coating thickness was 1071 m.
実施例−12 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-12 0 heating resistance layer The heating resistance layer of Example-3 was used.
○滑性耐熱層 まず以下の組成の塗液を用意した。○Smooth heat-resistant layer First, a coating liquid with the following composition was prepared.
実施例−4と同じ熱硬化性樹脂、増感剤。The same thermosetting resin and sensitizer as in Example-4.
溶媒を同じ量用意した。The same amount of solvent was prepared.
添加剤二弗素系界面活性剤メガファックF−184(大
日本インキ■製)1.5重量部添加剤: L−7005
1,5重量部
上記の塗液を実施例−4と同様に溶解し、バーコータで
塗工し、同様に乾燥硬化させて発熱体12を得た。塗工
厚みは3μmであった。Additive Difluorinated surfactant Megafac F-184 (manufactured by Dainippon Ink ■) 1.5 parts by weight Additive: L-7005
1.5 parts by weight The above coating liquid was dissolved in the same manner as in Example 4, coated with a bar coater, and dried and cured in the same manner to obtain a heating element 12. The coating thickness was 3 μm.
実施例−13 0発熱抵抗層 実施例−3の発熱抵抗層を用いた。Example-13 0 heating resistance layer The heating resistance layer of Example-3 was used.
○滑性耐熱層 まず以下の組成の塗液を用意した。○Smooth heat-resistant layer First, a coating liquid with the following composition was prepared.
実施例−12と同じ熱硬化性樹脂、増感剤。The same thermosetting resin and sensitizer as in Example-12.
添加剤、溶媒を同じ量用意した。The same amounts of additives and solvents were prepared.
粒子:弗化カーボンOF(ダイキン工業曲551)31
竜部
上記組成の塗料をボールミルで2時間分散して、上記発
熱抵抗層上に、バーコータで塗工し、溶剤を乾燥させた
後IKWの高圧水銀灯を2分間照射して硬化させて発熱
体13を得た。塗工厚みは371 mであった。Particles: Carbon fluoride OF (Daikin Kogyo 551) 31
Ryube: The paint having the above composition was dispersed in a ball mill for 2 hours, coated on the heat generating resistor layer with a bar coater, and after drying the solvent, it was irradiated with an IKW high-pressure mercury lamp for 2 minutes to cure, thereby forming the heat generating element 13. I got it. The coating thickness was 371 m.
比較例−1
実施例−1と同じ発熱抵抗層だけを用いて発熱体1′と
した。Comparative Example-1 A heating element 1' was prepared using only the same heating resistance layer as in Example-1.
比較例−2
実施例−2と同じ発熱抵抗層だけを用いて発熱体2′と
した。Comparative Example 2 A heating element 2' was prepared using only the same heating resistance layer as in Example 2.
比較例−3
実施例−3と同じ発熱抵抗層だけを用いて発熱体2′と
した。Comparative Example 3 A heating element 2' was prepared using only the same heating resistance layer as in Example 3.
上記の発熱体1〜132発熱体1′〜3′を用いて以下
示す記録条件で、ワックスタイプの転写シー)TCRC
/W(富士化学紙工業■製)を転写シートに、また記録
紙として熱転写用紙TTRPW(三菱製紙■製)とを用
いて、ベタ印字で通電記録を行った。Using the above heating elements 1 to 132 and heating elements 1' to 3', under the recording conditions shown below, perform a wax type transfer sheet) TCRC.
/W (manufactured by Fuji Kagaku Paper Industries ■) as a transfer sheet and thermal transfer paper TTRPW (manufactured by Mitsubishi Paper Industries ■) as a recording paper, and energization recording was performed by solid printing.
〈記録条件〉
○通電ヘッド ・・・16ドツト/ +−n m(分
離電極密度) (ラインヘッド)○記録周間
・・・0.4ms
○印加パルス幅 ・・・80 )t s○印加電圧
・・・39V
その結果を表に示す。<Recording conditions> ○Electric head...16 dots/+-nm (separated electrode density) (Line head) ○Recording period
...0.4ms ○Applied pulse width ...80 )t s○Applied voltage
...39V The results are shown in the table.
発熱体1−13と発熱体1′〜3′とを比較すると、本
発明の滑性耐熱層により連続記録ライン数が増えている
ことが解る。Comparing heating element 1-13 with heating elements 1' to 3', it can be seen that the number of continuous recording lines is increased due to the smooth heat-resistant layer of the present invention.
発熱体1〜3は、本発明の発熱抵抗層の形態の違いと連
続記録との関係を示す。フィルム基材自身を発熱抵抗層
とする(発熱体l、2)よりも、通電高抵抗層上に発熱
抵抗層を設けた形態(発熱体3)の方が連続記録ライン
数が増えることが解る。この原因は、フィルム自体を発
熱抵抗層とすると、加熱によ−る履歴が蓄積され、フィ
ルムが破壊されるためである。Heating elements 1 to 3 show the relationship between the different shapes of the heat generating resistive layer of the present invention and continuous recording. It can be seen that the number of continuous recording lines increases when the heating resistive layer is provided on the current-carrying high-resistance layer (heating element 3) than when the film base itself is used as the heating resistive layer (heating elements 1 and 2). . The reason for this is that if the film itself is used as a heat generating resistance layer, history due to heating will accumulate and the film will be destroyed.
発熱体4〜8は活性耐熱層の厚みの効果である。The heating elements 4 to 8 are an effect of the thickness of the active heat-resistant layer.
滑性耐熱層の厚みの効果で発熱体5は発熱体4に比べ、
14.000ライン延び、発熱体6は約2o、oooラ
イン延びた。しかし発熱体6は滑性耐熱層が15μmと
厚いため、印字記録感度が若干低かった。また発熱体7
と発熱体8とは、逆に滑性耐熱層が薄い場合についてで
ある。発熱体7は発熱体4に比へi、oooライン程度
減少しただけであったが、発熱体8は発熱体7に比べて
もは約40,000ライン減少した。この原因は、1゛
け性耐熱層に入れた添加剤の効果で、熱硬化性樹脂に対
して発熱体4は10重景%、発熱体9は0゜1重量%で
あるが、発熱体10は0.05重量%あることによる。Due to the effect of the thickness of the slippery heat-resistant layer, the heating element 5 has a lower temperature than the heating element 4.
14,000 lines were extended, and the heating element 6 was extended about 2o, ooo lines. However, since the heating element 6 had a thick lubricious heat-resistant layer of 15 μm, the print recording sensitivity was slightly low. Also, the heating element 7
and heating element 8, on the contrary, are for the case where the slippery heat-resistant layer is thin. Heating element 7 was only reduced by about i,ooo lines compared to heating element 4, but heating element 8 was reduced by about 40,000 lines compared to heating element 7. The cause of this is the effect of the additives added to the heat-resistant layer.Heating element 4 is 10% by weight and heating element 9 is 0.1% by weight relative to the thermosetting resin. 10 is due to the fact that it is 0.05% by weight.
発熱体11から明白なように、本発明の滑性耐熱層は紫
外線硬化型の熱硬化性樹脂以外の樹脂も適応できる。As is clear from the heating element 11, the lubricating heat-resistant layer of the present invention can be made of resins other than ultraviolet-curable thermosetting resins.
発熱体4と12とを比べると、複数種の添加剤を混入し
てもよいことがわかる。Comparing heating elements 4 and 12, it can be seen that multiple types of additives may be mixed.
発熱体12と13とを比較すると、発熱体13は連続記
録ライン数で94,000ライン増加している。これは
活性耐熱層に入れた粒子の効果である。Comparing heating elements 12 and 13, heating element 13 has an increased number of continuous recording lines by 94,000 lines. This is the effect of the particles placed in the active heat-resistant layer.
また本実施例および比較例では、電気的接触が恒常的に
保たれるため、印字抜けが発生しなかった。Further, in the present example and comparative example, since electrical contact was permanently maintained, no missing characters occurred.
なお本実施例および比較例においては、立ち上がりライ
ンと最終ラインとの濃度差もなく、記録周期0.4ms
の高速記録でも蓄熱がほとんど発生していなかった。Note that in this example and comparative example, there was no density difference between the rising line and the final line, and the recording period was 0.4 ms.
Even during high-speed recording, there was almost no heat accumulation.
また他の添加剤材料を加えた場合でも同様の結果が得ら
れた。Similar results were also obtained when other additive materials were added.
また他の感熱記録材料(例えば感熱記録紙、昇華性感熱
転写記録体等)を用いても同様の結果が得られた。Similar results were also obtained using other heat-sensitive recording materials (for example, heat-sensitive recording paper, sublimation heat-sensitive transfer recording material, etc.).
発明の効果
本発明の発熱体は、滑性耐熱層が弗素系、シリコーン系
もしくは酸アマイド系の離型剤か界面活性剤の内少なく
とも1種類の添加剤と熱硬化性樹脂とを含むため、記録
材料を安定にしかも長時間摺動させることができる。Effects of the Invention In the heating element of the present invention, the slippery heat-resistant layer contains at least one additive selected from a fluorine-based, silicone-based, or acid amide-based mold release agent or surfactant, and a thermosetting resin. The recording material can be slid stably and for a long time.
本発明の発熱体を用いた記録方法では、電気的接触を恒
常的に保てるために、記録中に印字抜けが発生しない効
果がある。In the recording method using the heating element of the present invention, electrical contact can be maintained permanently, so there is an effect that printing omissions do not occur during recording.
また市販の熱転写シートや感熱紙が使用できるたり、ラ
ンニングコストは低くできる効果がある。In addition, commercially available thermal transfer sheets and thermal paper can be used, and running costs can be reduced.
第1図〜第3図は、本発明の実施例における発熱体の構
成を示す断面図、第4図は本発明の発熱体を用いた記録
方式の構成を示す断面図である。
1・・・分離電極、 2・・・1Iffi還電極、3・
・・通電ヘッド、 4・・・発熱抵抗層、5・・・滑性
耐熱層、 6・・ 発熱体、7・・・感熱記録材料、
10・・・電極層、11・・・通電高抵抗層。
代理人の氏名 弁理士 中尾敏男 はか1名第 1 図
第 2 ロ
゛) 3 回
第 4 図1 to 3 are cross-sectional views showing the structure of a heating element in an embodiment of the present invention, and FIG. 4 is a cross-sectional view showing the structure of a recording method using the heat generating element of the present invention. 1...Separation electrode, 2...1Iffi return electrode, 3.
... Current-carrying head, 4... Heat-generating resistive layer, 5... Slippery heat-resistant layer, 6... Heating element, 7... Heat-sensitive recording material,
10... Electrode layer, 11... Current-carrying high resistance layer. Name of agent: Patent attorney Toshio Nakao (1 person) Figure 1 Figure 2 (Ro) 3rd Figure 4
Claims (5)
熱層が弗素系、シリコーン系、もしくは酸アマイド系の
離型剤か界面活性剤の内少なくとも1種類の添加剤と熱
硬化性樹脂とを含むことを特徴する発熱体。(1) A slippery heat-resistant layer is provided on the heat-generating resistance layer, and the slippery heat-resistant layer contains at least one additive selected from a fluorine-based, silicone-based, or acid amide-based mold release agent or a surfactant. A heating element characterized by comprising a curable resin.
けたことを特徴とする特許請求の範囲第1項記載の発熱
体。(2) The heating element according to claim 1, characterized in that an electrode layer is provided at the interface between the heating resistance layer and the slippery heat-resistant layer.
とを特徴とする特許請求の範囲第1項もしくは第2項記
載の発熱体。(3) The heating element according to claim 1 or 2, wherein the heating resistance layer is laminated on the current-carrying high resistance layer.
求の範囲第1項から第3項いずれにか記載の発熱体。(4) The heating element according to any one of claims 1 to 3, characterized in that the slippery heat-resistant layer contains particles.
囲であることを特徴とする特許請求の範囲第1項記載の
発熱体。(5) The heating element according to claim 1, wherein the additive is in a range of 0.1 to 10% by weight of the thermosetting resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62304805A JPH01146789A (en) | 1987-12-02 | 1987-12-02 | Heating body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62304805A JPH01146789A (en) | 1987-12-02 | 1987-12-02 | Heating body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01146789A true JPH01146789A (en) | 1989-06-08 |
Family
ID=17937456
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62304805A Pending JPH01146789A (en) | 1987-12-02 | 1987-12-02 | Heating body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01146789A (en) |
-
1987
- 1987-12-02 JP JP62304805A patent/JPH01146789A/en active Pending
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