WO1996002022A1 - Image-receiving film for electrography - Google Patents
Image-receiving film for electrography Download PDFInfo
- Publication number
- WO1996002022A1 WO1996002022A1 PCT/US1995/006958 US9506958W WO9602022A1 WO 1996002022 A1 WO1996002022 A1 WO 1996002022A1 US 9506958 W US9506958 W US 9506958W WO 9602022 A1 WO9602022 A1 WO 9602022A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- image
- film
- receiving
- silicone oil
- fatty acids
- Prior art date
Links
- 229920002545 silicone oil Polymers 0.000 claims abstract description 57
- 239000000758 substrate Substances 0.000 claims abstract description 34
- 239000003463 adsorbent Substances 0.000 claims abstract description 32
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 30
- 239000000194 fatty acid Substances 0.000 claims abstract description 30
- 229930195729 fatty acid Natural products 0.000 claims abstract description 30
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 30
- 150000002148 esters Chemical class 0.000 claims abstract description 13
- 239000000344 soap Substances 0.000 claims abstract description 9
- 150000001298 alcohols Chemical class 0.000 claims abstract description 7
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 7
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical group CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 claims description 24
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
- 229940114072 12-hydroxystearic acid Drugs 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 claims description 3
- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical group C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 claims description 2
- 229940087101 dibenzylidene sorbitol Drugs 0.000 claims description 2
- 238000003384 imaging method Methods 0.000 claims description 2
- 239000010408 film Substances 0.000 description 94
- 150000001875 compounds Chemical class 0.000 description 35
- 238000011176 pooling Methods 0.000 description 21
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- 239000002245 particle Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 238000010276 construction Methods 0.000 description 9
- 229920001225 polyester resin Polymers 0.000 description 9
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- 229920005989 resin Polymers 0.000 description 9
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- 239000011248 coating agent Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
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- 230000000052 comparative effect Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 6
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- 229920001577 copolymer Polymers 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 229920006255 plastic film Polymers 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 2
- 229940063655 aluminum stearate Drugs 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
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- 229910052739 hydrogen Inorganic materials 0.000 description 2
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- 230000014759 maintenance of location Effects 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
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- 239000002904 solvent Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 2
- 238000011179 visual inspection Methods 0.000 description 2
- CUXYLFPMQMFGPL-UHFFFAOYSA-N (9Z,11E,13E)-9,11,13-Octadecatrienoic acid Natural products CCCCC=CC=CC=CCCCCCCCC(O)=O CUXYLFPMQMFGPL-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-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
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
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- 239000005639 Lauric acid Substances 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
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- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
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- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
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- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 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
- 229940088990 ammonium stearate Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
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- 230000007423 decrease Effects 0.000 description 1
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- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- 238000007607 die coating method Methods 0.000 description 1
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- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
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- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- 235000011090 malic acid Nutrition 0.000 description 1
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
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- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
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- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
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- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 229940080350 sodium stearate Drugs 0.000 description 1
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- 239000001384 succinic acid Substances 0.000 description 1
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- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G7/00—Selection of materials for use in image-receiving members, i.e. for reversal by physical contact; Manufacture thereof
- G03G7/0006—Cover layers for image-receiving members; Strippable coversheets
- G03G7/002—Organic components thereof
Definitions
- the present invention relates to an image-receiving film for electrography. More particularly, it relates to a film useful for receiving an image formed by electrography.
- electrophotography used herein is intended to mean systems including electrophotography, electroradiography and magnetography, as widely recognized in the field of imaging and described in a number of patent documents and the like.
- the image- receiving film of the present invention can be usefully utilized for the preparation of an OHP film particularly by color electrophotography among the electrographic systems.
- Japanese Unexamined Patent Publication (Kokai) No. 5-173351 proposes an OHP film comprising a recording layer (an image-forming layer) having a capability of absorbing a silicone oil.
- the recording layer is composed mainly of a polymethacrylic ester/styrene copolymer (hydroxyl number: 40 or more) and a polymer of a quaternary ammonium salt.
- the capability of this film to absorb the silicone oil still remains low even when the hydroxyl number of the polymethacrylic ester/styrene copolymer used in the recording layer is 80.
- an image-receiving layer comprising a polymer film having a thickness of 0.5 to 10 ⁇ m, particles at least half of which have a particle diameter enough to protrude from the image-receiving layer (for example, silica particles having a particle diameter of about 10 ⁇ m) .
- this novel film comprises a substrate 11 comprising a transparent polyethylene terephthalate film and, provided on said substrate, an image-receiving layer 12 comprising a polyester resin containing silica particles 15.
- the silicone oil from the fixation roller is absorbed into the image-receiving layer 12 on its surface to form an oil layer 17.
- an object of the present invention is to provide an image-receiving film for electrography which enables the occurrence of an oil pooling phenomenon to be minimized (the inhibition of an oil pooling phenomenon) , the silicone oil once held on the image- receiving layer to remain held without rapid falling (an improvement in oil retention) and the transfer of the silicone oil, when touched by hand, to be reduced (a reduction in oiliness to the touch) .
- an imagereceiving film for electrography comprising a transparent substrate or support and an image-receiving layer or receptor layer provided on at least one surface of said substrate, wherein said image-receiving layer contains at least one silicone oil adsorbent selected from the group consisting of fatty acids, esters of fatty acids, derivatives of fatty acids and metallic soaps.
- an image- receiving film for electrography comprising a transparent substrate and an image-receiving layer provided on at least one surface of said substrate, wherein said image-receiving layer contains at least one silicone oil adsorbent selected from the group consisting of polyhydric alcohols, higher alcohols and higher dialcohols .
- an image-receiving film for electrography comprising a transparent substrate or support and an image-receiving layer or receptor layer provided on at least one surface of said substrate, wherein said i age- receiving layer has on its surface an overcoat layer, and said overcoat layer contains at least one silicone oil adsorbent selected from the group consisting of fatty acids, esters of fatty acids, derivatives of fatty acids and metallic soaps.
- an image-receiving film for electrography comprising a transparent substrate and an image-receiving layer provided on at least one surface of said substrate, wherein said imagereceiving layer has on its surface an overcoat layer, and said overcoat layer contains at least one silicone oil adsorbent selected from the group consisting of polyhydric alcohols, higher alcohols and higher dialcohols.
- the overcoat layer containing a silicone oil adsorbent may be provided on the image-receiving layer directly or alternatively through any intermediate layer.
- the thickness of the overcoat layer is preferably in the range of from 0.01 to 10 g/m 2 in terms of the coverage.
- Fig. 1 is a schematic cross-sectional view of a preferred embodiment of the image-receiving film according to the present invention.
- an image-receiving layer 2 and an overcoat layer 3 are successively provided on one surface of a transparent substrate 1.
- the overcoat layer 3 comprises a specific compound having a carboxyl group (fatty acids, esters of fatty acids, derivatives of fatty acids and metallic soaps) or a specific compound having a hydroxyl group (polyhydric alcohols, higher alcohols and higher dialcohols) .
- the image-receiving layer 2 and the overcoat layer 3 may be provided also on the opposite side of the substrate 1 although this is not shown in the drawing.
- a suitable transparent film may be properly selected from plastic films commonly used as a substrate in the art. in the production of an image-receiving film.
- the suitable substrate is preferably a heat-resistant plastic film, and examples thereof include films of polyethylene terephthalate, polyethylene naphthalate, polymethyl acrylate, polymethyl methacrylate, cellulose triacetate, plyamides, polyimides, polyvinyl chloride, polyvinylidene chloride, polystyrene and polycarbonate.
- the above-described plastic film may be subjected to a corona treatment or may have on its back surface a layer containing an antistatic agent.
- the thickness of the substrate is preferably in the range of from 10 to 200 ⁇ m.
- the thickness of the substrate is more preferably in the range of from 50 to 175 ⁇ m, most preferably in the range of from 75 to 150 ⁇ m. The regulation of the thickness of the substrate to the above-described range can offer a good balanced film construction and, at the same time, would reduce the cost per unit weight.
- a suitable material may be properly selected from resin materials commonly used as a material for an image- receiving layer in the art in the production of an irr.age- receiving film.
- a suitable material for the image- receiving layer is preferably a resin material which enables a toner, particularly a color toner, to be easily fused thereto and, at the same time, can provide an image having a high transparency.
- the suitable material include polyester resin, styrene/acrylic resin, epoxy resin, urethane resin and polyolefin resin. Among them, polyester resin is particularly preferred.
- the thickness of the image-receiving layer is preferably in the range of from 0.1 to 100 g/nr in terms of the coverage. When the thickness is less than 0.1 g/nr, it cannot receive the toner satisfactorily. On the other hand, when the thickness exceeds 100 g/m 2 , the light transmittance becomes low and, at the same time, the film cannot be carried smoothly within copying machines.
- the coverage of the image-receiving layer is more preferably in the range of from 0.5 to 10 g/m" most preferably in the range of from 0.1 to 5 g/m".
- the overcoat layer provided on the image-receiving layer contains at least one compound having a carboxyl group, selected from the group consisting of fatty acids, ester of fatty acids, derivatives of fatty acids and metallic soaps, as a silicone oil adsorbent.
- these silicone oil adsorbent compounds serve as a gelling agent for the silicone oil, that is, are substances which can cause gelation of the fed silicone oil by taking advantage of heat fed by the fixation roller. The gelation inhibits the migration of the silicone oil and, at the same time, reduces the oiliness on the surface of the film.
- Typical examples of the carboxyl group-containing compound (fatty acids, esters of fatty acids, derivatives of fatty acids and metallic soaps) useful as a silicone oil adsorbent in the present invention are as follows.
- the term "fatty acids” is intended to mean chain compounds having one carboxyl group, and include lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, montanic acid, oleic acid, linolenic acid, eleostearic acid, 12-hydroxystearic acid and the like.
- Esters of fatty acids is intended to mean ester compounds of the above-mentioned fatty acids with onoalcohols, dialcohols or trialcohols, and typical examples thereof include stearic glycerin ester, palmitic glycerin ester and the like.
- derivatives of fatty acids is intended to mean compounds containing one or more carboxyl groups in the molecular chain thereof exclusive of said fatty acids and esters thereof, and as examples thereof, there are mentioned phthalic acid, maleic acid, malic acid, succinic acid and the like.
- metal soaps is intended to mean metal salts of fatty acids, and include aluminum stearate, sodium stearate, potassium stearate, lead stearate, zinc stearate and the like.
- silicone oil adsorbent compounds palmitic acid, myristic acid, stearic acid, aluminum stearate and zinc stearate are easily available and inexpensive.
- 12-hydroxystearic acid has in its molecule a hydroxyl group as well as a carboxyl group, so that the silicone oil adsorption is better.
- the overcoat layer contains at least one compound selected from the group consisting of polyhydric alcohols, higher alcohols and higher dialcohols. More specifically, preferable examples of the hydroxyl group containing compound useful as a silicone oil adsorbent in the present invention include dibenzylidenesorbitol and 1,10 decanediol .
- the compounds exemplified above are suitable because they have a high capability of forming a hydrogen bond and a good silicone oil adsorption.
- silicone oil adsorvent compounds are generally used alone, however, if desired, a mixture of two or more types of the compounds may also be used in combination.
- Preferred compounds having a carboxyl group, as a silicone oil adsorbent to have a melting point of from 40 to 150°C and be solid at room temperature. When the melting point is below 40°C, the compound is liquid at room temperature, so that the resultant film has a pocr handleability. On the other hand, when the melting point exceeds 150°C, it becomes difficult to melt the compound at a temperature fed by the fixation roller, which results in difficulty in fixing the toner successfully.
- the above silicone oil adsorbent compounds are suitably soluble in a non-solvent for the image-receiving layer from the viewpoint of production of thelovercoat layer. Specifically, in general, they are soluble in a lower alcohol, glycerin or the like, which is a non-solvent for the image receiving layer. In this case, the overcoat layer can be easily formed without detriment to the i age-receivinq layer at the time of coating.
- the overcoat layer may further comprises a polyester resin, a styrene resin and the like in addition to the above described compounds having a carboxyl group or a hydroxyl group as a silicone oil adsorbent.
- additional resins are useful for improving the adhesion of the overcoat layer to the underlayer (image-receiving layer) . In this case, however, precautions should be taken so as not to lower the transparency of the overcoat layer.
- the use (as the additional resin) of a resin identical to or in the same type as the resin for the image-receiving layer is advantageous in that the improvement in adhesion is significant and no lowering in receptivity to the image is observed.
- the thickness of the overcoat layer comprising a silicone oil adsorbent compound is preferably in the range of from 0.01 to 10 g/m " in terms of the coverage. When the coverage is less than 0.01 g/nr, the effect of adsorbing the silicone oil is small. On the other hand, when it exceeds 10 g/m", the light transmittance is likely to be lowered.
- the coverage of the overcoat layer is more preferably in the range of from 0.1 to 1 g/m-, most preferably in the range of from 0.3 to 0.8 g/m". The regulation of the coverage of the overcoat layer in the above-described range offers a good balanced film construction and, at the same time, facilitates the formation of the overcoat layer.
- the image-receiving film according to the above embodiment has an additional advantage over an image- receiving film without an overcoat layer, in that a satisfactory effect can be attained using a very small amount of silicone oil adsorbent (compound having a carboxyl group or compound having a hydroxyl group) .
- the image-receiving film without an overcoat layer also has an additional advantage over the image- receiving film of the above embodiment in that the simple layer construction simlifies the production process and a thin film can be provided.
- Fig. 2 is a schematic cross-sectional view of another preferred embodiment of the image-receiving film of the present invention.
- the image-receiving film according to this embodiment comprises a transparent substrate 1 and, on one surface of the substrate, an image-receiving layer 4 comprising a silicone oil adsorbent (compound having a carboxyl group or compound having a hydroxyl group) .
- an image-receiving layer 4 comprising a silicone oil adsorbent (compound having a carboxyl group or compound having a hydroxyl group) .
- the image-receiving film shown in Fig. 2 may further comprise any additional layer (not shown) .
- the transparent substrate 1 may be the same as that in the image-receiving film shown in Fig. 1. Further, the image-receiving layer 4 and, the silicone oil adsorbent incorporated therein may also be the same as those used in the image-receiving film shown in Fig. 1.
- the useful amount of the silicone oil adsorbent compound added is from 1 to 1000 parts by weight based on 100 parts by weight of the remaining resin in the image-receiving layer. When it is less than 1 part by weight, the intended effect cannot be attained; when it exceeds 1000 parts by weight, the light transmittance is lowered, which is likely to cause a lowering in image quality and haze development.
- the preferred amount of the compound (s) is from 10 to 500 parts by weight, most preferably in the range of from 30 to 300 parts by weight.
- Fig. 3 is a schematic cross-sectional view of a further preferred embodiment of the image-receiving film of the present invention.
- the image-receiving film according to this embodiment has the same construction as in Fig. 1, except that the image-receiving layer 2 provided on the transparent substrate 1 contains fine particles 5 (silica particles in this case) and is covered with the overcoat layer 3.
- the overcoat layer 3 comprises a silicone oil adsorbent (compound having a carboxyl group or compound having a hydroxyl group) . Fine particles include silica particles and fine particles of various other inorganic and organic materials are useful.
- Suitable examples of the fine particles include those of silica, alumina, calcium carbonate, diatomaceous earth, plymethacrylate and polystyrene.
- the incorporation of these fine particles into the image-receiving layer are favorable from the viewpoint of reducing the oil pooling phenomenon and more smoothly carrying the film (i.e., improving the feedability of the film) within copying machines.
- the silica particles When the silica particles are incorporated into the image-receiving layer, they may be in the form of a primary particle or an aggregate of particles.
- the particle diameter of the silica particles or aggregate may be preferably in the range of from 1 to 100 ⁇ m. When it is less than 1 ⁇ m, the effect of reducing the oil pooling phenomenon is poor and an improvement in feedability is small. When it exceeds 100 ⁇ m, the light transmittance is lowered, which results in an increase in haze.
- the particle diameter is more preferably in the range of from 5 to 50 ⁇ m, most preferably in the range of from 8 to 25 ⁇ m.
- the silica particle contains the above- described silicone oil adsorbent (compound having a carboxyl group or compound having a hydroxyl group) .
- silicone oil adsorbent compound having a carboxyl group or compound having a hydroxyl group.
- the silicone oil adsorbent compounds are incorporated into the image-receiving film in this way, the particles are protruded on the surface of image- receiving film. The intended effect can be attained even when the amount of the silicone oil adsorbent compound (s) added is small, and the effect is maintained, so that there is no fear of the light transmittance being lowered.
- silica particles may be incorporated into the overcoat layer instead of or in addition to the image receiving layer. This is suitable from the viewpoint of reducing the oil pooling phenomenon and improving the feedability of the film, and when added to the overcoat layer, the effect seen from the particles is larger for the amount added.
- the antistatic effect of the film can be enhanced by adding an antistatic agent to any layer constituting the image-receiving film.
- useful antistatic agents include quaternary ammonium salts and various clay particles.
- the addition of the antistatic agent reduces the surface resistivity of the image-receiving film. Therefore, the amount of the antistatic agent added is preferably determined by taking the surface resistivity of the film into consideration.
- the surface resistivity varies depending upon the specific copying machine used, it is suitably in the range of from 1 x 10 8 to 1 x 10 ⁇ . When it is less than 1 x 10 r ⁇ , the transfer of the toner is poor. On the other hand, when it exceeds 1 x 10 14 ⁇ , the film cannot be smoothly carried within copying machines.
- the surface resistivity is more preferably in the range of from 1 x 10 '' to 1 x 10 lj ⁇ .
- the image-receiving film of the present invention may be prepared by various techniques depending upon film layer construction and other factors.
- an image-receiving layer is formed by coating directly on a substrate film, and drying. After the resultant coating is dried, a solution of the selected silicone oil adsorbent and an antistatic agent dissolved in ethanol are coated.
- the coating operation may be carried out by coating methods commonly used in the art, such as Mayer bar coating, B & M extrusion coating, die coating, Narr coating, gravure coating and k ss coating.
- 12-Hydroxystearic acid is soluble in an oil at the melting point or above.
- the temperature decreases with time, which causes molecules to be arranged through a hydrogen bend in a three-dimensional manner, so that a network structure 6 similar to that of polymeric compounds i ⁇ formed as a whole.
- a silicone oil 7 is incorporated in the network structure 6 and gels. As a result, the migration of silicone oil is prevented, which contributes to a reduction in surface oiliness cf the film.
- a transparent polyester resin was coated on a 125 ⁇ m thick transparent polyester film (a substrate) at a coverage of 2.5 g/m' to form an image-receiving layer. Then, a solution of 94.5 g of 12-hydroxystearic acid and 12.6 g of an antistatic agent comprising a quaternary ammonium salt dissolved in 3043 g of ethanol was coated thereon by extrusion coating to form an overcoat layer. The coverage of the overcoat layer on a dry basis was 0.5 g/m" .
- An image was formed on the resultant image-forming film by means of a color copying machine. The imaged film was used as an OHP film to evaluate the properties.
- Laser Copia CLC200 (a registered trade mark) (a color laser copying machine manufactured by Canon Sales Co., Inc.) was used as the color copying machine.
- Example 2 The procedure of Example 1 was repeated, except that an image-receiving layer was formed by coating a solution of 300 g of a polyester resin (PS-2 manufacture ⁇ oy Kao Corp.) and 6.0 g of a polyester resin (VITEL 2200 manufactured by Goodyear Tire & Rubber Co.) as an adhesive composition for improving the adhesion to a toner, dissolved m 1347 g of toluene and 1347 g of methyl ethyl ketone. The coverage of the image-receiving layer was 2.5 g/m .
- a polyester resin PS-2 manufacture ⁇ oy Kao Corp.
- VITEL 2200 manufactured by Goodyear Tire & Rubber Co.
- Example 3 The procedure of Example 1 was repeated, except that instead of 12-hydroxystearic acid, the following compounds were used in the same amounts as 12-hydroxy stearic acid.
- Example 3 dibenzyl-dienesorbitol
- Example 4 ammonium stearate
- Example 5 zinc stearate
- Example 6 stearic acid
- Example 7 1, 10-decanediol
- Example 8 The procedure of Example 1 was repeated, except that the antistatic agent used was a commercially available antistatic agent as noted below used in the same amounts as the antistatic agent used in Example 1.
- Example 8 Electrostopper QE (a cationic antistatic agent manufactured by Kao Corp.)
- Chemistat 3033 an anionic antistatic agent manufactured by Sanyo Kasei Kcgyo K.K.
- Example 10 Adekamine (a cationic antistatic agent manufactured by Asahi Denka Kogyo Ltd.)
- Example 11 The procedure of Example 1 was repeated, except that the coverage of the overcoat layer was changed as fellows.
- Example 11 0.1 g/irr
- Example 12 1 g/m
- Example 13 A solution of 0.50 g of 12-hydroxystearic acid, J.50 g of a polyester resin (PS-1 manufactured by Kao Corp.), 0.01 g of a polyester resin (VITEL 1200 manufactured by Goodyear Tire & Rubber Co.), 0.015 g of an antistatic agent derived from a quaternary ammonium salt dissolved in 2.16 g of toluene and 2.16 g of methyl ethyl ketone was coated using a #12 Mayer bar on a 125 ⁇ m thick transparent polyethylene terephthalate film (a substrate) at a coverage of 2.5 g/nr to form an image-receiving layer.
- PS-1 manufactured by Kao Corp.
- VITEL 1200 manufactured by Goodyear Tire & Rubber Co.
- 0.015 g of an antistatic agent derived from a quaternary ammonium salt dissolved in 2.16 g of toluene and 2.16 g of methyl ethyl ketone was coated using
- Example 1 13 Good Good Good Good Good Comparative Examples 1 and 2
- the procedure of Example 1 was repeated, except that, for comparison, 12-hydroxystearic acid was not added to the overcoat layer and the coverage of the overcoat layer was changed as follows.
- Comparative Example 1 0.5 g/m"
- Comparative Example 2 0.1 g/nr
- Table 2 The results are given in the following Table 2.
- a solution comprising 20 parts by weight of the copolymer, 20 parts by weight of a polymer of a quaternary ammonium salt (Elecond PQ-50B manufactured by Soken Chemical Engineering Co., Ltd.), 30 parts by weight of toluene and 30 parts by weight of methyl isobutyl ketone was prepared and coated on a 5 mil-thick polyethylene terephthalate film at a coverage of 5 g/m" on a dry basis.
- the image-receiving film thus obtained was unsatisfactory in silicone oil adsorption and other properties.
- the occurrence of an oil pooling phenomenon can be reduced, and a silicone oil, which has been once held on an image-receiving layer, can be kept on the image-receiving layer.
- the film construction is simple, and all the materials used are easily available and inexpensive, which contributes to a lowering in product cost.
- Fig. 1 is a schematic cross-sectional view of a preferred embodiment of the image-receiving film for electrography according to the present invention.
- Fig. 2 is a schematic cross-sectional view of another preferred embodiment of the image-receiving film for electrography according to the present invention.
- Fig. 3 is a schematic cross-sectional view of another preferred embodiment of the image-receiving film for electrography according to the present invention.
- Fig. 3 is a schematic cross-sectional view of a further preferred embodiment of the image-receiving film for electrography according to the present invention.
- Fig. 4 is a schematic diagram showing typical gelation of a silicone oil according to the present invention.
- Fig. 5 is a schematic cross-sectional view showing an embodiment of the conventional image-receiving film for electrography.
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Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95921570A EP0770229A1 (en) | 1994-07-08 | 1995-06-02 | Image-receiving film for electrography |
AU26605/95A AU2660595A (en) | 1994-07-08 | 1995-06-02 | Image-receiving film for electrography |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP157190/94 | 1994-07-08 | ||
JP15719094A JPH0830009A (en) | 1994-07-08 | 1994-07-08 | Image-receiving film for electrography |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996002022A1 true WO1996002022A1 (en) | 1996-01-25 |
Family
ID=15644176
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/006958 WO1996002022A1 (en) | 1994-07-08 | 1995-06-02 | Image-receiving film for electrography |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0770229A1 (en) |
JP (1) | JPH0830009A (en) |
CN (1) | CN1151795A (en) |
AU (1) | AU2660595A (en) |
CA (1) | CA2193219A1 (en) |
WO (1) | WO1996002022A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0778500A1 (en) * | 1995-12-08 | 1997-06-11 | Canon Kabushiki Kaisha | Light-transmitting recording material for electrophotography, and heat fixing method |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3951080B2 (en) * | 1998-10-07 | 2007-08-01 | セイコーエプソン株式会社 | Image receiving sheet and image forming apparatus using the same |
-
1994
- 1994-07-08 JP JP15719094A patent/JPH0830009A/en active Pending
-
1995
- 1995-06-02 CN CN 95193934 patent/CN1151795A/en active Pending
- 1995-06-02 WO PCT/US1995/006958 patent/WO1996002022A1/en not_active Application Discontinuation
- 1995-06-02 EP EP95921570A patent/EP0770229A1/en not_active Withdrawn
- 1995-06-02 CA CA 2193219 patent/CA2193219A1/en not_active Abandoned
- 1995-06-02 AU AU26605/95A patent/AU2660595A/en not_active Abandoned
Non-Patent Citations (1)
Title |
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DATABASE WPI Derwent World Patents Index; * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0778500A1 (en) * | 1995-12-08 | 1997-06-11 | Canon Kabushiki Kaisha | Light-transmitting recording material for electrophotography, and heat fixing method |
Also Published As
Publication number | Publication date |
---|---|
AU2660595A (en) | 1996-02-09 |
EP0770229A1 (en) | 1997-05-02 |
CA2193219A1 (en) | 1996-01-25 |
CN1151795A (en) | 1997-06-11 |
JPH0830009A (en) | 1996-02-02 |
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