JPH0150900B2 - - Google Patents
Info
- Publication number
- JPH0150900B2 JPH0150900B2 JP57230069A JP23006982A JPH0150900B2 JP H0150900 B2 JPH0150900 B2 JP H0150900B2 JP 57230069 A JP57230069 A JP 57230069A JP 23006982 A JP23006982 A JP 23006982A JP H0150900 B2 JPH0150900 B2 JP H0150900B2
- Authority
- JP
- Japan
- Prior art keywords
- dielectric layer
- release agent
- pressure fixing
- electrostatic recording
- acid
- 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.)
- Expired
Links
- 239000000463 material Substances 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000001993 wax Substances 0.000 claims description 9
- -1 fatty acid ester Chemical class 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 229930195729 fatty acid Natural products 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 229920002050 silicone resin Polymers 0.000 claims description 5
- 229920002545 silicone oil Polymers 0.000 claims description 4
- 239000000344 soap Substances 0.000 claims description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 238000000576 coating method Methods 0.000 description 17
- 238000000034 method Methods 0.000 description 17
- 239000011248 coating agent Substances 0.000 description 12
- 239000002245 particle Substances 0.000 description 11
- 239000007788 liquid Substances 0.000 description 10
- 239000006082 mold release agent Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 6
- 239000008116 calcium stearate Substances 0.000 description 6
- 235000013539 calcium stearate Nutrition 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000011161 development Methods 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001940 conductive polymer Polymers 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 239000005518 polymer electrolyte Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 229940037312 stearamide Drugs 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
- RLLIKXPTKNBNBZ-YXAHYSCSSA-N 2-methylpropyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC(C)C RLLIKXPTKNBNBZ-YXAHYSCSSA-N 0.000 description 1
- RVYJGPQZGSBHAH-UHFFFAOYSA-N 2-pentyldodecanoic acid Chemical compound CCCCCCCCCCC(C(O)=O)CCCCC RVYJGPQZGSBHAH-UHFFFAOYSA-N 0.000 description 1
- PHUSOTFVZQDLMC-QXMHVHEDSA-N 3-methylbutyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCC(C)C PHUSOTFVZQDLMC-QXMHVHEDSA-N 0.000 description 1
- YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- RSSGSPAYFRXVKG-UHFFFAOYSA-N Tridecanamide Chemical compound CCCCCCCCCCCCC(N)=O RSSGSPAYFRXVKG-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
- IYDRZGXWJPJSNY-UHFFFAOYSA-N decyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCC IYDRZGXWJPJSNY-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- JOSJZPLSVYWPAG-UHFFFAOYSA-L dodecanoate;nickel(2+) Chemical compound [Ni+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O JOSJZPLSVYWPAG-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- CMDXMIHZUJPRHG-UHFFFAOYSA-N ethenyl decanoate Chemical compound CCCCCCCCCC(=O)OC=C CMDXMIHZUJPRHG-UHFFFAOYSA-N 0.000 description 1
- 229940093470 ethylene Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- MFCQPVRHCQCFBB-UHFFFAOYSA-N heptyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCCCCCC MFCQPVRHCQCFBB-UHFFFAOYSA-N 0.000 description 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- VEIWYFRREFUNRC-UHFFFAOYSA-N hydron;piperidine;chloride Chemical compound [Cl-].C1CC[NH2+]CC1 VEIWYFRREFUNRC-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011806 microball Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QEALYLRSRQDCRA-UHFFFAOYSA-N myristamide Chemical compound CCCCCCCCCCCCCC(N)=O QEALYLRSRQDCRA-UHFFFAOYSA-N 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- QXYWIOWTBOREMG-UHFFFAOYSA-N nonadecan-2-ol Chemical compound CCCCCCCCCCCCCCCCCC(C)O QXYWIOWTBOREMG-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- FTBUKOLPOATXGV-UHFFFAOYSA-N propyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCC FTBUKOLPOATXGV-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 description 1
- 229940039790 sodium oxalate Drugs 0.000 description 1
- 229940006186 sodium polystyrene sulfonate Drugs 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229940012185 zinc palmitate Drugs 0.000 description 1
- GJAPSKMAVXDBIU-UHFFFAOYSA-L zinc;hexadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O GJAPSKMAVXDBIU-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/0202—Dielectric layers for electrography
- G03G5/0217—Inorganic components
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/10—Bases for charge-receiving or other layers
- G03G5/101—Paper bases
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Fixing For Electrophotography (AREA)
- Photoreceptors In Electrophotography (AREA)
Description
本発明は静電記録体に関し、特に粉体像を圧力
定着する際に優れた適応性を示す圧力定着用静電
記録体に関するものである。
静電記録法は導電処理を施した支持体上に絶縁
性樹脂などからなる誘導体層を設けた静電記録体
の誘電体層の前面、背面あるいは両面から電圧パ
ルスを印加するか、あるいは他の原板に形成され
た静電潜像を転写する方法によつて誘電体層上に
静電潜像を形成し、これをトナーによつて現像可
視化せしめる方法であり、フアクシミリ、プリン
ターなどに広く用いられている。
かかる静電記録体における静電潜像の現像法は
粉体現像法と液体現像法とに大別される。粉体現
像法は、一般に粉体トナーで現像したのち記録体
を熱オーブン間に通引させて粉体像を熱定着させ
るため、立上り時の温度不足に起因する定着不良
を生じやすく、また、装置の高速化に伴つてより
高温加熱を必要とし火災の危険がある等の欠点を
有する。一方、溶媒中にトナー粒子を分散させた
液体トナーを用いる液体現像法においてはトナー
の定着性が必ずしも充分ではなく、また有機溶剤
を用いるために火災の危険、臭気等の難点があ
る。
これらの難点を解決する方法として、近年、粉
体現像したのちの記録体を加圧された金属ロール
間に通引せしめトナー粒子を加圧変形させること
により記録体表面の誘導体層に固着せしめる所謂
圧力定着法が注目されている。
しかし、この圧力定着法においては、加圧定着
する際に本来記録体表面に定着させるべきトナー
粒子の一部が定着用の金属ロールに付着してロー
ル汚れを起したり、さらにはそのトナー粒子が再
度記録体上に転移してゴースト画像を生ずる所謂
オフセツト現象を発生するといつた問題がある。
この対策として、トナー粒子の定着性改良あるい
はワツクス等を添加して金属ロールに対するトナ
ー粒子の離型性を付与するなどトナー組成に関す
る改良のほか、シリコーンオイルを含浸させた布
で金属ロールを絶えずクリーニングして金属ロー
ルの離型性を保持するなど装置面での改善も検討
されている。しかしながら、これらの改良には改
良に伴い新たな難点が付随する。即ち、トナー粒
子の定着性改良やワツクス添加は電磁気的特性、
流動性あるいは保存安定性などのトナー粒子に基
本的に要求される特性に多大の影響を及ぼし、ま
た、金属ロールをクリーニングする方法は経時的
に効果が低下しメンテナンス上問題がある。
かかる現状に鑑み本発明者等は、トナー及び記
録体の電気的特性を損なうことなく、かつメンテ
ナンスフリーで圧力定着時のオフセツト現像を解
消する方法について鋭意検討の結果、本発明を完
成するに至つた。
本発明は、導電性支持体の片面に誘導体層を設
けてなる圧力定着用静電記録体において、該導電
性支持体のもう一方の面が特許請求の範囲で特定
する離型剤で処理されていることを特徴とする圧
力定着用静電記録体である。
前記離型剤の具体的な物質としては、プラスチ
ツク、ゴムなどの成型業界等において離型剤ある
いは滑剤として使用される種々の物質を用いるこ
とができ、例えば以下が例示される。
ステアリン酸亜鉛、ステアリン酸カルシウム、
ステアリン酸バリウム、ステアリン酸アルミニウ
ム、ステアリン酸マグネシウム、ステアリン酸亜
鉛・ステアリン酸カルシウム複合体、パルミチン
酸亜鉛、ラウリン酸鉛、ラウリン酸ニツケルなど
の金属石けん、ステアリン酸アミド、ステアリン
酸エチレンビスアミド、パルミチン酸アミド、ト
リデシル酸アミド、ラウリン酸アミド、ミリスチ
ン酸アミドなどの脂肪酸アミド、カプリン酸ビニ
ル、ラウリン酸プロピル、ミリスチン酸ヘプチ
ル、パルミチン酸デシル、オレイン酸イソアミ
ル、リシノール酸イソブチル、1,17―ヘプタデ
カメチレンジカルボン酸―ジ―n―ドデシルなど
の脂肪酸エステル系ワツクス、パラフインワツク
ス、ポリエチレンワツクス、マイクロクリスタリ
ンワツクス、塩素化パラフインワツクスなどの脂
肪族炭化水素系ワツクス、ステアリン酸、カプリ
ン酸、ラウリン酸、2,2―ジメチルドデカン
酸、2―ペンチルドデカン酸、ミリストレイン酸
などの高級脂肪酸、ラウリルアルコール、ミリス
チルアルコール、ステアリルアルコール、ノナデ
カン―2―オール、グリセリン、ソルビタンなど
の高級脂肪族アルコール、シリコーンレジン、シ
リコーンオイルおよびこれらの乳化物等。
これらの離型剤のうちでも金属石けん、脂肪酸
アミド、脂肪族酸炭化水素系ワツクス、シリコー
ンレジン、シリコーンオイルおよびこれらの乳化
物は、均一な処理液が得られかつ処理効果に優れ
るため特に好ましく用いられ、なかでも導電性支
持体に処理・乾燥された時点で固体状態のもの
は、誘導体層への転移もしくは拡散が起らずトナ
ーの定着性を損なう恐れがないためとりわけ好ま
しく用いられる。
本発明において、離型剤で処理された導電性支
持体を得る方法については特に限定するものでは
なく、導電性支持体の少なくとも誘電体層と接し
ない面に離型剤が処理されていればよい。必要に
応じて誘電体層と接しない面にも導電層を設ける
ような場合には、離型剤をかかる導電層中に混合
したり、或いは導電層上に改めて処理してもよ
い。この際に用いられる処理液は、離型剤を適当
な媒体中に溶解または分散させ、更に必要に応じ
て接着剤、顔料、導電性高分子電解質などの導電
性物質等を添加して調製される。かくして調製さ
れた処理液の処理方法としてはバーコーター、エ
ヤーナイフコーター、プレードコーター等による
塗布方法のみならずサイズプレス等による含浸方
法も可能であるが、好ましくは塗布方法によつて
処理される。
本発明における離型剤の処理量は、定着用ロー
ルの材質および構成、トナー粒子の特性、使用す
る離型剤の種類等によつて異なり一概には決めら
れないが、少量では効果がなく、逆に多過ぎると
金属ロールへの転移が過剰になりロール滑り、か
み込み不良などの通紙トラブルが発生するばかり
でなく記録体自体の滑りなどによるハンドリング
適性が低下する恐れもあるため、離型剤として一
般には0.001〜2g/m2、好ましくは0.01〜1
g/m2の範囲となるように処理されるのが望まし
い。
本発明では上述の如く誘電体層とは反対の面が
特定量の離型剤で処理されているものであるが、
それにもかかわらず圧力定着時に誘電体層上で発
生するオフセツト現象が極めて効果的に防止され
るのは、次のような機構によるものと考えられ
る。即ち、本発明の記録体が定着用ロール間で加
圧される際に、記録体裏面側に接するロールに適
量の離型剤が転移し、次いでこの転移された離型
剤が空運転時などに誘電体層側に接するロールへ
更に転移し、結果的に誘電体層側のロールに適度
な離型剤がつねに付与されるためと考えられる。
而して、本発明の記録体によれば、誘電体層を
離型剤処理する場合の如く誘電体層の電気的特性
あるいはトナーの定着性が阻害されることはな
く、極めて効果的にオフセツト現象が防止される
ものである。
本発明において、導電性支持体を調製する際に
使用される導電性物質は特に限定されるものでは
なく、静電記録体の分野で一般に用いられる物質
を使用することができ、例えば、ポリビニルベン
ジルトリメチルアンモニウムクロライド、ポリメ
タクリロキシエチルトリメチルアンモニウムクロ
ライド、ポリメタクリルオキシエチルジメチル―
β―ヒドロキシエチルアンモニウムクロライド、
ポリ(N,N―ジメチル―3,5―メチレン)ピ
ペリジニウムクロライド、ポリスチレンスルフオ
ン酸ソーダ等の導電性高分子電解質、アルミニウ
ム、ガリウム、インジウムをドープした酸化亜
鉛、アンチモンをドープした酸化錫、錫をドープ
した酸化インジウム、ヨウ化銅等の電子伝導性粉
末、塩化ナトリウム、塩化カリウム、シヨウ酸ナ
トリウム、塩化カルシウム、水酸化ナトリウム、
水酸化カリウム、水酸化カルシウム等の無機化合
物等が挙げられる。
本発明において、上記の如き導電性物質は水中
に溶解ないし分散することによつて塗液として調
製されるが塗液調製に際しては本発明の効果をさ
またげない範囲で、例えばポリビニルアルコー
ル、メチルセルロース、ヒドロキシエチルセルロ
ース、カルボキシメチルセルロース、澱粉、変性
澱粉、ポリビニルピロリドン、アルギン酸ソー
ダ、ポリアクリルアミド、スチレン・ブタジエン
共重合体ラテツクス、酢酸ビニル系ラテツクス、
アクリル酸系ラテツクスなどのノニオン、弱アニ
オンおよびカチオン系ラテツクス、スチレン・無
水マレイン酸共重合体塩、イソブテン・無水マレ
イン酸共重合体塩等の接着剤や炭酸カルシウム、
硫酸バリウム、酸化チタン、クレー、カオリン、
ゼオライト、酸化アルミニウム、酸化ケイ素、水
酸化アルミニウム、ポリスチレンマイクロボール
等の無機及び有機顔料、分散剤、消泡剤、染料、
および紫外線吸収剤等の各種助剤を必要に応じて
適宜添加することもできる。かくして得られた塗
液は紙、合成紙など通常の支持基体上に処理さ
れ、少なくとも誘導体層に接する面に導電層が形
成されて導電性支持体が調製される。
支持基体への塗液の処理方法としてはバーコー
ター、エヤーナイフコーター、ブレードコーター
等による塗布方法のみならずサイズプレス等によ
る含浸方法も可能であるが好ましくは塗布方法に
よつて処理される。処理量は、導電性支持体の表
面電気抵抗値が常湿で106〜109オームとなるよう
に調節され、通常乾燥重量で2〜20g/m2、好ま
しくは3〜15g/m2の範囲で塗布ないし含浸され
る。
本発明において誘電体層を形成するための塗液
としては有機溶剤系、水性分散系をとわず例えば
酢酸ビニル樹脂、塩化ビニル樹脂、シリコン樹
脂、エポキシ樹脂、アクリル樹脂、ポリエステル
樹脂、ブチラール樹脂、酢酸ビニル・クロトン酸
共重合体、スチレン・ブタジエン共重合体、塩化
ビニル・酢酸ビニル共重合体、塩化ビニリデン・
塩化ビニル共重合体、塩化ビニリデン・アクリロ
ニトリル共重合体等の絶縁性樹脂の単独あるいは
混合物の有機溶剤溶液あるいは水性分散液が例示
されるが、かかる塗液については本発明の圧力定
着用静電記録体において特に限定して使用される
ものではなく、適宜公知の絶縁性樹脂の中から選
択して使用可能であり、また塗液中に通常含有さ
れる助剤、例えばクレー、カオリン、タルク、炭
酸カルシウム、硫酸バリウム、炭酸バリウム、酸
化チタン、酸化亜鉛、アルミナ、焼成クレーおよ
びこれらをオルガノポリシロキサンあるいは牛脂
等によつて処理した無機顔料、重合体微粒子、澱
粉粉末、染料などを添加することは勿論除外する
ものではなく、また塗布方法も慣用の塗布装置を
以て行われ得る。塗布量についても特に限定され
ないが、一般に乾燥重量で2〜10g/m2好ましく
は4〜7g/m2の範囲で調節される。
以下に実施例を挙げて本発明をさらに具体的に
説明するが、勿論これらに限定されるものではな
い。また特にことわらない限り、例中の部および
%はそれぞれ重量部および重量%をあらわす。
実施例 1
米坪50g/m2の上質紙の片面に、ポリビニルベ
ンジルトリメチルアンモニウムクロライドの33%
水溶液(ダウケミカル社製、商品名ECR―34)
を乾燥塗布量が3g/m2となるように塗布・乾燥
した。次いでその上に、炭酸カルシウム(備北粉
化社製、商品名ソフトン1800)40部とブチラール
樹脂(積水化学社製、商品名BMS)60部とを混
合し25%トルエン溶液としたものを乾燥塗布量が
5g/m2となるように塗布・乾燥して誘電体層を
形成した。次いで、誘電体層を設けた面とは反対
の上質紙面上に、ポリビニルベンジルトリメチル
アンモニウムクロライドの33%水溶液(ダウケミ
カル社製、商品名ECR―34)100部(固形分換
算)、炭酸カルシウム(備北粉化社製、商品名ソ
フトン1800)50部、離型剤としてステアリン酸カ
ルシウムのエマルジヨン(サンノプコ社製、商品
名ノプコートC―104)10部(固形分換算)およ
び水850部を充分混合して得た塗液を乾燥塗布量
が2g/m2となるように塗布・乾燥して圧力定着
用静電記録紙を得た。
比較例 1
実施例1において、ステアリン酸カルシウムの
エマルジヨンを使用しなかつた以外は実施例1と
全く同様に行つた圧力定着用静電記録紙を得た。
比較例 2
実施例1において、ステアリン酸カルシウムの
エマルジヨンの使用量を固形分換算で0.05部とし
た以外は実施例1と同様にして圧力定着用静電記
録紙を得た。
実施例 2〜5
実施例1において、ステアリン酸カルシウムの
エマルジヨンの代りにシリコーンレジンのエマル
ジヨン(信越化学社製、商品名ポロンC)10部
(実施例2)、ポリエチレンワツクスのエマルジヨ
ン(アライドケミカル社製、商品名A・Cポリエ
チレン)30部(実施例3)、ステアリン酸アミド
のエマルジヨン(中京油脂社製、商品名セロゾー
ル187N)15部(実施例4)、および自己乳化性グ
リセリンモノステアレート粉末(花王アトラス社
製、アラツセル165)100部(実施例5)をそれぞ
れ離型剤として使用した以外は実施例1と全く同
様に実施して4種類の圧力定着用静電記録紙を得
た。なお、実施例2〜4における使用量は固形分
換算値を表わす。
かくして得られた7種類の圧力定着用静電記録
紙を、圧力定着用ロールが充分にクリーニングさ
れたフアクシミリ装置(松下電送社製、UF―
520)にて、電子写真学会No.2テストチヤートを
用いコピーモードで連続30通ずつ記録した。な
お、1試料30通の記録が終了する毎に、圧力定着
用ロールは充分にクリーニングした。そして、オ
フセツト現象の発生状況を評価しその結果を第1
表に示した。
The present invention relates to an electrostatic recording material, and more particularly to an electrostatic recording material for pressure fixing that exhibits excellent adaptability when pressure fixing powder images. In the electrostatic recording method, a voltage pulse is applied from the front, back, or both sides of the dielectric layer of an electrostatic recording medium in which a dielectric layer made of insulating resin or the like is provided on a support that has been subjected to conductive treatment, or other methods are used. This is a method of forming an electrostatic latent image on a dielectric layer by transferring the electrostatic latent image formed on the original plate, and making it visible by developing it with toner, and is widely used in facsimiles, printers, etc. ing. Methods for developing electrostatic latent images on such electrostatic recording materials are broadly classified into powder development methods and liquid development methods. In the powder development method, the recording medium is generally developed with a powder toner and then passed through a heating oven to thermally fix the powder image, which tends to cause fixing failures due to insufficient temperature at startup. As the speed of the device increases, it requires higher temperature heating, which has the disadvantage of causing a fire risk. On the other hand, in a liquid developing method using a liquid toner in which toner particles are dispersed in a solvent, the fixing properties of the toner are not necessarily sufficient, and since an organic solvent is used, there are disadvantages such as fire danger and odor. In recent years, as a method to solve these difficulties, a so-called method has been developed in which the recording material after powder development is passed between pressurized metal rolls, and the toner particles are deformed under pressure and fixed to the dielectric layer on the surface of the recording material. The pressure fixing method is attracting attention. However, in this pressure fixing method, during pressure fixing, some of the toner particles that should originally be fixed on the surface of the recording medium adhere to the fixing metal roll, causing roll stains, and furthermore, the toner particles There is a problem in that a so-called offset phenomenon occurs in which the particles are transferred onto the recording medium again and a ghost image is generated.
As a countermeasure, in addition to improving the toner composition, such as improving the fixing properties of the toner particles or adding wax or the like to give the toner particles release properties from the metal roll, we also constantly clean the metal roll with a cloth impregnated with silicone oil. Improvements in equipment, such as maintaining the releasability of metal rolls, are also being considered. However, these improvements come with new difficulties. In other words, improving the fixing properties of toner particles and adding wax depend on electromagnetic properties,
This has a great influence on the properties fundamentally required of toner particles, such as fluidity and storage stability, and the method of cleaning metal rolls becomes less effective over time and poses maintenance problems. In view of the current situation, the inventors of the present invention have conducted extensive studies on a method for eliminating offset development during pressure fixing without impairing the electrical properties of toners and recording materials and without maintenance, and as a result, they have completed the present invention. Ivy. The present invention provides an electrostatic recording material for pressure fixing comprising a conductive support provided with a dielectric layer on one side, in which the other side of the conductive support is treated with a release agent specified in the claims. This is an electrostatic recording material for pressure fixing, which is characterized in that: As specific materials for the mold release agent, various materials used as mold release agents or lubricants in the molding industry of plastics, rubber, etc. can be used, and examples thereof include the following. Zinc stearate, calcium stearate,
Metal soaps such as barium stearate, aluminum stearate, magnesium stearate, zinc stearate/calcium stearate complex, zinc palmitate, lead laurate, nickel laurate, stearamide, ethylene bisamide stearate, palmitic acid amide, Fatty acid amides such as tridecylic acid amide, lauric acid amide, myristic acid amide, vinyl caprate, propyl laurate, heptyl myristate, decyl palmitate, isoamyl oleate, isobutyl ricinoleate, 1,17-heptadecamethylene dicarboxylic acid. Fatty acid ester wax such as G-n-dodecyl, aliphatic hydrocarbon wax such as paraffin wax, polyethylene wax, microcrystalline wax, chlorinated paraffin wax, stearic acid, capric acid, lauric acid, 2, Higher fatty acids such as 2-dimethyldodecanoic acid, 2-pentyldodecanoic acid, myristoleic acid, higher aliphatic alcohols such as lauryl alcohol, myristyl alcohol, stearyl alcohol, nonadecan-2-ol, glycerin, sorbitan, silicone resin, silicone oil and emulsions thereof, etc. Among these mold release agents, metal soaps, fatty acid amides, aliphatic acid hydrocarbon waxes, silicone resins, silicone oils, and emulsions thereof are particularly preferably used because they provide a uniform treatment solution and have excellent treatment effects. Among them, those in a solid state after being processed and dried on a conductive support are particularly preferably used because they do not transfer or diffuse into the dielectric layer and there is no risk of impairing the fixing properties of the toner. In the present invention, the method for obtaining a conductive support treated with a mold release agent is not particularly limited, as long as at least the surface of the conductive support not in contact with the dielectric layer is treated with a mold release agent. good. If a conductive layer is to be provided on a surface not in contact with the dielectric layer, if necessary, a mold release agent may be mixed into the conductive layer or may be treated anew on the conductive layer. The processing liquid used at this time is prepared by dissolving or dispersing the mold release agent in a suitable medium, and further adding adhesives, pigments, conductive substances such as conductive polymer electrolytes, etc. as necessary. Ru. The treatment solution thus prepared can be treated not only by a coating method using a bar coater, an air knife coater, a blade coater, etc., but also by an impregnation method using a size press, etc., but preferably by a coating method. The amount of release agent to be treated in the present invention varies depending on the material and structure of the fixing roll, the characteristics of toner particles, the type of release agent used, etc., and cannot be determined unconditionally, but a small amount will not be effective. On the other hand, if the amount is too large, the transfer to the metal roll will be excessive, which will not only cause paper feeding problems such as roll slippage and poor biting, but also may reduce handling suitability due to slipping of the recording body itself, so release the mold. Generally 0.001 to 2 g/m 2 , preferably 0.01 to 1
It is preferable that the treatment be carried out in such a way that the amount is within the range of g/m 2 . In the present invention, as mentioned above, the surface opposite to the dielectric layer is treated with a specific amount of mold release agent,
Despite this, the offset phenomenon that occurs on the dielectric layer during pressure fixing is extremely effectively prevented, which is thought to be due to the following mechanism. That is, when the recording medium of the present invention is pressurized between fixing rolls, an appropriate amount of the release agent is transferred to the roll that is in contact with the back side of the recording medium, and then this transferred release agent is transferred during idle operation, etc. This is thought to be because the release agent is further transferred to the roll in contact with the dielectric layer, and as a result, an appropriate amount of mold release agent is always applied to the roll on the dielectric layer side. Therefore, according to the recording medium of the present invention, the electrical properties of the dielectric layer or the toner fixing properties are not inhibited unlike when the dielectric layer is treated with a release agent, and offset can be extremely effectively achieved. The phenomenon is to be prevented. In the present invention, the conductive substance used in preparing the conductive support is not particularly limited, and substances commonly used in the field of electrostatic recording materials can be used, such as polyvinylbenzyl Trimethylammonium chloride, polymethacryloxyethyltrimethylammonium chloride, polymethacryloxyethyldimethyl-
β-hydroxyethylammonium chloride,
Conductive polymer electrolytes such as poly(N,N-dimethyl-3,5-methylene)piperidinium chloride, sodium polystyrene sulfonate, zinc oxide doped with aluminum, gallium, and indium, tin oxide doped with antimony, Electronically conductive powders such as tin-doped indium oxide and copper iodide, sodium chloride, potassium chloride, sodium oxalate, calcium chloride, sodium hydroxide,
Examples include inorganic compounds such as potassium hydroxide and calcium hydroxide. In the present invention, the conductive substances described above are prepared as a coating liquid by dissolving or dispersing them in water. When preparing the coating liquid, for example, polyvinyl alcohol, methyl cellulose, hydroxy Ethylcellulose, carboxymethylcellulose, starch, modified starch, polyvinylpyrrolidone, sodium alginate, polyacrylamide, styrene-butadiene copolymer latex, vinyl acetate latex,
Nonionic, weak anionic and cationic latexes such as acrylic acid latexes, adhesives such as styrene/maleic anhydride copolymer salts, isobutene/maleic anhydride copolymer salts, calcium carbonate,
barium sulfate, titanium oxide, clay, kaolin,
Inorganic and organic pigments such as zeolite, aluminum oxide, silicon oxide, aluminum hydroxide, polystyrene microballs, dispersants, antifoaming agents, dyes,
Various auxiliary agents such as ultraviolet absorbers may also be added as necessary. The coating liquid thus obtained is applied onto a common support substrate such as paper or synthetic paper, and a conductive layer is formed at least on the surface in contact with the dielectric layer, thereby preparing a conductive support. The coating solution can be applied to the supporting substrate not only by a coating method using a bar coater, an air knife coater, a blade coater, etc., but also by an impregnating method using a size press, etc., but preferably by a coating method. The amount of treatment is adjusted so that the surface electrical resistance value of the conductive support is 10 6 to 10 9 ohms at normal humidity, and the dry weight is usually 2 to 20 g/m 2 , preferably 3 to 15 g/m 2 . Painted or impregnated over a range of areas. In the present invention, the coating liquid for forming the dielectric layer may be organic solvent-based or aqueous dispersion, such as vinyl acetate resin, vinyl chloride resin, silicone resin, epoxy resin, acrylic resin, polyester resin, butyral resin, Vinyl acetate/crotonic acid copolymer, styrene/butadiene copolymer, vinyl chloride/vinyl acetate copolymer, vinylidene chloride/
Examples include organic solvent solutions or aqueous dispersions of insulating resins such as vinyl chloride copolymer, vinylidene chloride/acrylonitrile copolymer, etc., alone or as a mixture. It is not particularly limited in use in the body, and can be selected from among known insulating resins, and auxiliary agents normally contained in coating liquids, such as clay, kaolin, talc, and carbonic acid, can be used. Of course, calcium, barium sulfate, barium carbonate, titanium oxide, zinc oxide, alumina, calcined clay, inorganic pigments prepared by treating these with organopolysiloxane or beef tallow, polymer particles, starch powder, dyes, etc. can be added. This is not excluded, and the coating method can also be carried out using conventional coating equipment. The amount of coating is also not particularly limited, but is generally adjusted in a dry weight range of 2 to 10 g/m 2 , preferably 4 to 7 g/m 2 . The present invention will be explained in more detail with reference to Examples below, but it is of course not limited thereto. Further, unless otherwise specified, parts and % in the examples represent parts by weight and % by weight, respectively. Example 1 33% of polyvinylbenzyltrimethylammonium chloride was applied to one side of a 50 g/ m2 high-quality paper.
Aqueous solution (manufactured by Dow Chemical Company, product name ECR-34)
was applied and dried so that the dry coating amount was 3 g/m 2 . Next, a 25% toluene solution made by mixing 40 parts of calcium carbonate (manufactured by Bihoku Funka Co., Ltd., trade name: Softon 1800) and 60 parts of butyral resin (manufactured by Sekisui Chemical Co., Ltd., trade name: BMS) was then dried and applied on top. A dielectric layer was formed by coating and drying in an amount of 5 g/m 2 . Next, 100 parts (solid content equivalent) of a 33% aqueous solution of polyvinylbenzyltrimethylammonium chloride (manufactured by Dow Chemical Company, trade name ECR-34), calcium carbonate ( Thoroughly mix 50 parts of Softon 1800 (manufactured by Bihoku Funka Co., Ltd., trade name), 10 parts (solid content equivalent) of calcium stearate emulsion (manufactured by San Nopco Co., Ltd., trade name Nopcoat C-104) as a mold release agent, and 850 parts of water. The obtained coating liquid was applied and dried to a dry coating amount of 2 g/m 2 to obtain an electrostatic recording paper for pressure fixing. Comparative Example 1 An electrostatic recording paper for pressure fixing was obtained in exactly the same manner as in Example 1 except that the emulsion of calcium stearate was not used. Comparative Example 2 An electrostatic recording paper for pressure fixing was obtained in the same manner as in Example 1, except that the amount of calcium stearate emulsion used was 0.05 part in terms of solid content. Examples 2 to 5 In Example 1, instead of the calcium stearate emulsion, 10 parts of a silicone resin emulsion (manufactured by Shin-Etsu Chemical Co., Ltd., trade name Poron C) (Example 2) and a polyethylene wax emulsion (manufactured by Allied Chemical Co., Ltd.) were used. , trade name A/C polyethylene) 30 parts (Example 3), 15 parts of stearamide emulsion (manufactured by Chukyo Yushi Co., Ltd., trade name Cellozol 187N) (Example 4), and self-emulsifying glycerin monostearate powder ( Four types of electrostatic recording paper for pressure fixing were obtained in exactly the same manner as in Example 1, except that 100 parts of Aratsucel 165 (manufactured by Kao Atlas Co., Ltd.) (Example 5) was used as a release agent. Note that the amounts used in Examples 2 to 4 represent solid content conversion values. The seven types of electrostatic recording paper for pressure fixing obtained in this way were transferred to a facsimile machine (manufactured by Matsushita Densen Co., Ltd., UF-
520), 30 consecutive copies were recorded in copy mode using the Electrophotography Society No. 2 test chart. The pressure fixing roll was thoroughly cleaned every time recording of 30 copies of one sample was completed. Then, evaluate the occurrence of the offset phenomenon and use the results as the first
Shown in the table.
【表】
第1表の結果から明らかな如く、本発明の圧力
定着用静電記録体は、オフセツト現象の発生が極
めて効果的に防止された優れた記録体であつた。[Table] As is clear from the results in Table 1, the electrostatic recording medium for pressure fixing of the present invention was an excellent recording medium in which the occurrence of offset phenomenon was extremely effectively prevented.
Claims (1)
圧力定着用静電記録体において、該導電性支持体
のもう一方の面が金属石けん、脂肪酸アミド、脂
肪酸エステル系ワツクス、脂肪族炭化水素系ワツ
クス、高級脂肪酸、高級脂肪族アルコール、シリ
コーンレジン、シリコーンオイルおよびこれらの
乳化物のうちのいずれかの離型剤で処理されてい
ることを特徴とする圧力定着用静電記録体。1. In a pressure fixing electrostatic recording material comprising a dielectric layer provided on one side of a conductive support, the other side of the conductive support is made of metal soap, fatty acid amide, fatty acid ester wax, or aliphatic hydrocarbon. 1. An electrostatic recording material for pressure fixing, characterized in that it is treated with a release agent selected from waxes, higher fatty acids, higher aliphatic alcohols, silicone resins, silicone oils, and emulsions thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23006982A JPS59121339A (en) | 1982-12-28 | 1982-12-28 | Electrostatic recording body for pressure fixing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23006982A JPS59121339A (en) | 1982-12-28 | 1982-12-28 | Electrostatic recording body for pressure fixing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59121339A JPS59121339A (en) | 1984-07-13 |
JPH0150900B2 true JPH0150900B2 (en) | 1989-11-01 |
Family
ID=16902049
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23006982A Granted JPS59121339A (en) | 1982-12-28 | 1982-12-28 | Electrostatic recording body for pressure fixing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59121339A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53112741A (en) * | 1977-03-12 | 1978-10-02 | Tomoegawa Paper Co Ltd | Image receiving sheet |
JPS55140848A (en) * | 1979-04-20 | 1980-11-04 | Kanzaki Paper Mfg Co Ltd | Electrostatic recording body |
JPS5633651A (en) * | 1979-08-28 | 1981-04-04 | Ricoh Co Ltd | Electrostatic recording body |
JPS5646154A (en) * | 1979-09-21 | 1981-04-27 | Ricoh Co Ltd | Carriage driving mechanism |
-
1982
- 1982-12-28 JP JP23006982A patent/JPS59121339A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53112741A (en) * | 1977-03-12 | 1978-10-02 | Tomoegawa Paper Co Ltd | Image receiving sheet |
JPS55140848A (en) * | 1979-04-20 | 1980-11-04 | Kanzaki Paper Mfg Co Ltd | Electrostatic recording body |
JPS5633651A (en) * | 1979-08-28 | 1981-04-04 | Ricoh Co Ltd | Electrostatic recording body |
JPS5646154A (en) * | 1979-09-21 | 1981-04-27 | Ricoh Co Ltd | Carriage driving mechanism |
Also Published As
Publication number | Publication date |
---|---|
JPS59121339A (en) | 1984-07-13 |
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