Detailed Description Of The Invention
[electrophotographic image reception thin slice]
In detail referring to accompanying drawing, Fig. 1 specifically, it has shown that a kind of electrophotographic image of the electronic photographing device (this paper back is referred to as fixedly banding pattern electronic photographing device with it) be used to having fixed band receives thin slice 1, and this electrophotographic image receives lip-deep toner image receiving layer 2 and the backing layer as required 4 that thin slice 1 comprises carrier 3, is coated on carrier 3. Toner image receiving layer 2 contains a releasing agent. Electrophotographic image receive thin slice 1 can be separately or any combination provide other different layers such as sealer, intermediate layer, undercoating, cushion, antistatic control or antistatic layer, reflecting layer, color key-course, bin stability raising layer, anti-adhesive layer, anti-roll boundary layer, smooth layer etc.
<carrier 〉
Carrier 3 has no particular limits it, can select for any purpose, without any special restriction. Available have various paper and a thin slice, such as body paper, synthetic paper, synthetic resin thin slice, coated paper, laminated paper etc. Any carrier can be single layer structure or laminar structure.
This paper back is illustrated the material of carrier 3.
Body paper:
Optionally use conventional known body paper and the material of synthetic paper, without any special restriction. These materials comprise the natural pulp that is made by coniferous tree or broad leaf tree, synthetic plastic paper pulp such as polyethylene and polypropylene, or the mixture of natural pulp and synthetic paper-pulp. For surface flatness, rigidity, the dimensional stability (hemming performance) that fully improves body paper in the mode of equilibrium, the broad leaf tree kraft pulp (LBKP) of rinsing is the desirable paper pulp as former paper material. Yet, also can use the coniferous tree kraft pulp (NBKP) of rinsing or the sulfite pulp of broad leaf tree. And, according to staple length, preferably utilize the paper pulp of broad leaf tree as primary raw material. Paper pulp in beater mill or lapping machine through preliminary treatment. Add various additives such as filler, dry tenacity hardening agent, sizing agent, wet strength hardening agent, fixer, pH adjusting agent and other conditioner to refining pulp slurry (it is referred to as pulp slurry in some cases). The preferred embodiment of filler includes, but not limited to calcium carbonate, clay, kaolin, carclazyte, talcum, titanium oxide, diatomite, barium sulfite, aluminium hydroxide, magnesium hydroxide etc. The preferred embodiment of dry tenacity hardening agent include, but not limited to through cation exchange starch, through the polyacrylamide of cation exchange, the polyacrylamide, amphiprotic polyacrylamide through anion exchange, carboxy-modified POLYPROPYLENE GLYCOL etc. The preferred embodiment of sizing agent comprises, but be not limited to rosin derivative (such as soap, rosin, rosin maleate etc.), paraffin and have higher fatty acids such as the compound of alkyl ketene dimer, alkenyl, anhydrous succinic acid (ASA), epoxidized fatty acid acid amides etc. The preferred embodiment of wet strength hardening agent includes, but not limited to polyamine daiamid epoxy chloropropane, melamine resin, carbamide resin, epoxidized polyamide resin etc. The preferred embodiment of fixer includes, but not limited to slaine such as aluminum sulfate, aluminium chloride, polyvalent cation polymer as through the starch of cation exchange etc. The preferred embodiment of PH conditioning agent includes, but not limited to caustic soda, sodium carbonate etc. The preferred embodiment of other conditioner includes, but not limited to defoamer, dyestuff, foundry loam controlling agent, fluorescent whitening agent etc. And if necessary, pulp slurry can add (1980 by the Paper and Chemicals Times publication) described in softening agent such as the New Paper Coating Handbook 554-555 page or leaf.
The solution that is used for surperficial starching processing can contain water-soluble polymer, sizing agent, waterproof material, pigment, pH adjusting agent, dyestuff, fluorescent whitening agent etc. The preferred embodiment of water-soluble polymer comprises, but be not limited to, through the starch of cation exchange, polyvinyl alcohol, carboxy-modified polyvinyl alcohol, carboxymethyl cellulose, hydroxyethylcellulose, cellulose sulfuric acid ester, gelatin, casein, Sodium Polyacrylate, styrene-dehydration sodium maleate copolymer, kayexalate etc. The preferred embodiment of waterproof material includes, but not limited to latex emulsion such as SB, vinyl-vinyl acetate copolymer, polyethylene, dichloroethylene etc., polyamide polyamine epichlorhydrin etc. The preferred embodiment of pigment includes, but not limited to calcium carbonate, clay, kaolin, talcum, barium sulfite, titanium oxide etc.
Except above-mentioned natural pulp papers, the body paper raw material comprises synthetic paper-pulp paper, natural and synthetic mixed pulp paper and various extrusion coating paper.
In order to improve rigidity and the dimensional stability (hemming performance) that receives thin slice for the image of xerography, desirable body paper has the Young's modulus of 1.5-2.0 than Ea/Eb (Ea: vertical Young's modulus; Eb: horizontal Young's modulus). If surpass this upper limit and/or lower limit, can damage rigidity and hemming performance that image receives thin slice, and have influence on its transportation performance.
Being used for picture-side surface (being coated with toner image receiving layer 2 on it) that image receives the body paper of thin slice 1 has Oken grade greater than 210 seconds (it is the value of measuring according to JAPAN TAPPI Rule No.5B, this paper back is referred to as the Oken smoothness) smoothness, the visual surface flatness that it significantly is coated with greater than routine was more preferably greater than 250 seconds. If the Oken smoothness was less than 210 seconds, image receives the mass defect that thin slice 1 causes toner image. Toner image layer 2 is coated to the Oken smoothness can reaches required effect greater than the image reception thin slice 1 that obtains on 20 seconds the body paper. Although the Oken smoothness is not had the upper limit, yet the Oken smoothness is more preferably less than 500 seconds in fact ideally less than 600 seconds.
Known in general, the rigidity of paper is difference with the type of the refining of the paper pulp of preparation paper. Be can be used as the key factor of the paper rigidity that representative makes by refining paper pulp by the elastic modelling quantity of the paper of refining paper pulp preparation. Specifically, the speed of sound wave that the elastic force of paper (elastic modelling quantity) can ultrasonic transducer produces and that propagate by paper be basic, utilizes the dynamic elastic modulus (a kind of viscoplasticity solid state properties) of paper and the relation between the density to draw. That is, the elastic modelling quantity of paper provides by following numerical expression:
E=ρc
2(1-n
2)
Wherein E is dynamic elastic modulus;
ρ is density;
C is the SVEL of propagating by paper;
N is Poisson's ratio.
In this case, consider that conventional paper has about 0.2 Poisson's ratio, the elastic modelling quantity of paper can be gone out by following numerical expression approximate calculation:
E=ρc
2
That is, as long as know density harmony wave propagation velocity, just can easily calculate the elastic modelling quantity of paper. The spread speed of sound wave in paper is by various commercially available Instrument measurings known in the art. The Sonic Tester SST 110 that for example, can use Normura Co., Ltd to produce.
Require body paper to have preferred 30-500 μ m, more preferably the thickness of 100-250 μ m, preferably 50-250g/cm2, more preferably 100-200g/cm2Basis weight. The preferred embodiment of these body paper comprises, but be not limited to the Fundamental Photographic Engineering-Silver Salt Photography that high quality paper and Japanese photograph association edit (1978 published by CORONASHA Co., Ltd) the listed paper of 223-240 page or leaf.
In order to make the base paper sheet mask that desirable center line average roughness be arranged, preferred use have the fiber length distribution described in the Japanese unexamined patent publication No. publication number 58-68037 for example paper pulp (for example, the residual volume of crossing the fiber of 24 mesh sieves is the 20-45 % by weight with the residual volume sum of crossing 42 mesh sieves, and the residual volume of crossing the fiber of 24 mesh sieves is 5 % by weight). This center line average roughness can be by being regulated through heat and pressure treatment surface with calender or supercalender.
The synthetic resin thin slice
The preferred embodiment of the material of synthetic resin thin slice includes, but not limited to vistanex such as acrylic resin, mylar such as polyethylene terephthalate resin. The synthetic resin thin slice is made by the sheet extruder of this materials'use shape.
Coated paper
Coated paper is the coating that applies a kind of different resins by the one or both sides to paper such as body paper, is thermoplastic resin, rubber latex and polymkeric substance and paper or the thin slice made ideally.Coating weight is difference with required purposes.The preferred embodiment of coated paper is art paper, casting film paper, Yang Qi paper etc.The coating of thermoplastic resin is preferably 5-100 μ m, more preferably 15-50 μ m.In composition, solid state properties, thickness and configuration aspects, the coating that is coated in the thermoplastic resin on the two sides of paper or thin slice can be mutually the same or different.
The preferred embodiment rough segmentation of thermoplastic resin becomes (1)-(8) group.
(1) resin of the multipolymer of polyvinyl resin, polyolefin resin such as acrylic resin, alkene such as ethene or propylene and vinyl monomer.
(2) has the thermoplastic resin of ester bond: for example, vibrin with dicarboxylic acid (can replace) component and alkoxide component (can replace) condensation acquisition with hydroxyl with sulfonic acid group or carboxyl, polyacrylate resin or polymethacrylate resin such as polymethylmethacrylate, poly-n-butyl methacrylate, polymethyl acrylate, butyl polyacrylate etc., polycarboxylate resin, vinylite, styrene-acrylate resin, styrene-methacrylate copolymer, vinyltoluene acrylate resin etc.
The more specifically example of thermoplastic resin for example is disclosed among Japanese unexamined patent publication No. publication number 59-101395,60-294862,63-7971,63-7972 and the 63-7973.Commercially available thermoplastic resin includes, but not limited to Vyron 103,200,280,290,300, GK-130 and GK-140 (being produced by Toyobo company limited); Tafuton NE-382, U-5, ATR-2009 and ATR-2010 (producing) by Kao company limited; Elitel UE3500, UE3210, XA-8153, KZA-7049 and KZA-1449 (producing) by Unitika company limited; PolyesterTP-220 and R-188 (producing) by ippon synthetic chemical industry company limited; The thermoplastic resin of Hyros series (producing) by Seiko chemical industry company limited;
(3) urethane resin;
(4) polyamide, carbamide resin;
(5) polysulfone resin;
(6) Corvic, polyvinyl dichloride resin, vinyl chloride vinyl acetate copolymer resin, vinyl chloride-vinyl propionate ester copolymer resin;
(7) polyol resin such as polyvinyl butyral, celluosic resin such as ethyl cellulose resin, cellulose ethanoate resin;
(8) polycaprolactone resin, phenylethylene-maleic anhydride resin, polyacrylonitrile resin, polyether resin, epoxy resin, phenol resin.
These thermoplastic resins can use separately or two or more combination in any is used.
Laminated paper
Laminated paper is with laminated material such as polyolefin, Polyvinylchloride, polyethylene terephthalate, polystyrene, polymethacrylate, polycarbonate, polyimide, triacetyl cellulose etc., separately or the thin slice that makes of two or more combination in any laminations with former paper sheet and resin flake or film, rubber sheet or film or polymer flake or film.
Usually polyolefin is made with low density polyethylene.Yet, have the thermotolerance of raising in order to make carrier 3, it is desirable to potpourri that uses polypropylene, polypropylene and poly potpourri, high density polyethylene, high density polyethylene and low density polyethylene or the like.Specifically, with regard to cost and lamination adaptability, the more preferably potpourri of high density polyethylene and low density polyethylene.The mixing ratio of high density polyethylene and low density polyethylene (weight ratio) preferably 1: 9-9: 1, more preferably 2: 8-8: 2, most preferably be 3: 7-7: 3.All be coated with under the situation of thermoplastic resin on the two sides of carrier 3, the back side of carrier 3 (relative with visual receiving plane) preferably made by the potpourri of high density polyethylene or high density polyethylene and low density polyethylene.In this case, tygon is not subjected to the molecule quantitative limitation, yet it is desirable to have the melting index of 1.0-40g/10min, higher density or low-density tygon, and have the good adaptability of extruding.These thin slices or film can be through handling to have white light reflection.This processing realizes by pigment such as titanium dioxide are sneaked in thin slice or the film.
Coating or the resin used of lamination are not limited to thermoplastic resin, and can comprise the resin monomer polymerization produced with heat or light and be added the resin of producing with heat or light reaction after rigidizer or the crosslinking chemical by thermoplastic resin.At least a coating or laminate layers can be to contain the monomer of Photoepolymerizationinitiater initiater or the resin combination that solidifies with the ultraviolet ray irradiation.In this case, be example with the resin combination, it is a kind of resin that contains the electronic radiation solidifying organic compound as initial component.This electronic radiation solidifying organic compound is not subjected to the special restriction of type, monomer or oligomer, and can use separately or two or more combination in any uses.
This electronic radiation solidifying organic compound can be selected from following (1)-(7) group compound.
(1) monohydroxy alcohol is to the poly alkylene glycol of the acyclic compound of hexahydroxylic alcohols and aliphatics, alicyclic or aromatic-aliphatic;
(2) add the acyclic compound of the monohydroxy alcohol of aliphatics that the alkylene oxide adjuvant is arranged, alicyclic or aromatic-aliphatic to hexahydroxylic alcohols;
(3) polypropylene acyl group alkyl phosphate class;
(4) carboxylic acid, polyvalent alcohol and acrylic acid reaction product;
(5) isocyanates, polyvalent alcohol and acrylic acid reaction product;
(6) epoxy compound and acrylic acid reaction product;
(7) epoxy compound, polyvalent alcohol and acrylic acid reaction product.
The instantiation of these electronic radiation solidifying organic compounds comprises, but be not limited to, the bisphenol a diacrylate that polyoxyethylene is epoxychloropropane modified, the dicyclohexyl acrylate, epoxychloropropane modified polyethyleneglycol diacrylate, 1, the 6-hexanediyl ester, hydroxyl two L-valine ester neopentylglycol diacrylates, the Nonylphenoxy polyethylene glycol acrylate, the phenates phosphoester acrylic ester of ethylene oxide modification, the phthalic acid acrylate of ethylene oxide modification, the PBAA ester, the tetrahydrofurfuryl acrylate of caprolactam modification, three (acryloxy ethyl) isocyanates, trimethylolpropane triacrylate, pentaerythritol triacrylate, tetramethylol methane tetraacrylate, pentaerythrite five acrylate, dipentaerythritol acrylate, polyethyleneglycol diacrylate, 1, the 4-butanediol diacrylate, neopentylglycol diacrylate, the trimethylolpropane diacrylate of neopentyl glycol modification etc.These organic compounds can use separately or two or more combination in any are used.
Be used to be coated with or the ultraviolet curing organic compound of the resin bed of lamination is not subjected to the concrete restriction of type.This ultraviolet curable resin composition makes by Photoepolymerizationinitiater initiater is suitably joined in the above-mentioned electronic radiation solidifying organic compound.The resin combination that is used for electronic radiation solidifying can contain Photoepolymerizationinitiater initiater or can not contain Photoepolymerizationinitiater initiater.The desirable amount of Photoepolymerizationinitiater initiater is in the scope of its flavor that do not give out a foul smell.
The preferred embodiment of Photoepolymerizationinitiater initiater include, but not limited to well-known in the art those, EAQ particularly; Acetophenones such as benzoyl methyl formate, 1-hydroxycyclohexylphenylketone, anthryl phenyl ketone (anthophenone), diethoxy anthryl phenyl ketone and trichlorine ethyl phenyl ketone; O-benzoyl yl benzoic acid methyl esters; Benzophenone; Michler's keton; Benzyl; Diphenylhydroxyethanone; The diphenylhydroxyethanone alkyl ether; The benzyl dimethyl ketal; Xanthones; The thioxanthene ketone; Benzophenones; Azo-compound or the like.These Photoepolymerizationinitiater initiaters can use separately or two or more combination in any are used.In ultraviolet curable resin, the amount of Photoepolymerizationinitiater initiater it is desirable to 0.1-10 weight %.It is desirable to use photopolymerization accelerator well-known in the art, for example N methyldiethanol amine or two diethylamino benzophenone are with this Photoepolymerizationinitiater initiater.As long as reached its acceleration effect, always this photopolymerization accelerator is not added quantitative limitation.Usually the preferred 0.5-2 photopolymerization accelerator doubly that uses the amount that is about Photoepolymerizationinitiater initiater.
The electron accelerator that is used for electron irradiation is not subjected to the special restriction of type.The preferred embodiment of electron-beam accelerator is Van de Graaff scanning electron radiator, two scanning electron radiator, heavy curtain bundle scanning electron radiator or the like.Ultraviolet radiator is not subjected to the specific limited of type.The preferred embodiment of ultraviolet radiator is low pressure mercury lamp, medium pressure mercury lamp, high-pressure sodium lamp, metal halide lamp etc.
Carrier 3 can be the laminate carrier of various carriers.For application of resin coating on body paper, preferably be coated on resin solution or resin suspension on the body paper or be sprayed onto on the body paper, perhaps soak body paper with resin solution or resin suspension.Preferably an opposite face or two opposite faces to body paper activate processing as Corona discharge Treatment, flame treatment, glow discharge processing or Cement Composite Treated by Plasma, to improve the bonding of resinous coat or laminate layers and body paper.On the also preferred surface, perhaps on coating that forms on body paper, synthetic paper or the synthetic resin thin slice or laminate layers, carry out surface treatment such as Corona discharge Treatment or undercoat to body paper, synthetic paper or synthetic resin thin slice.
If necessary, the thermoplastic resin that is coated on the coated paper can be polished to required surface texturisation such as glossy surface, thin surperficial as disclosed mat surface among the Japanese unexamined patent publication No. publication number 55-26507 or silk control surface.Can be polished to mat surface if necessary with the thermoplastic resin on the surperficial relative reverse side that is coated with the conduction coating layer.In addition, can activate processing to the polished surface of this thermoplastic resin as Corona discharge Treatment or flame cleaning.Afterwards, for example can also apply disclosed internal coating among the Japanese unexamined patent publication No. publication number 61-846443 to the activating surface of this thermoplastic resin.These processing can apply separately or can two or more combinations apply.This thermoplastic resin can contain the various adjuvants through suitably selecting in satisfying the scope of the object of the invention.
The preferred 25 μ m-300 μ m of the thickness of carrier 3, more preferably 50 μ m-260 μ m, 75 μ m-220 μ m most preferably, and can have rigidity according to application type.The electrophotographic image that is used to have the photographic image quality receives the carrier of thin slice, preferably near those of the color film that is used to cut into slices.
Aspect fixed performance, carrier 3 has the coefficient of heat conductivity that is higher than 0.50kcal/m.h. ℃ and is higher than 0.7g/cm
3Mass density.In this case, coefficient of heat conductivity can use the transfer paper humidity that disclosed method is nursed one's health by mensuration among the Japanese unexamined patent publication No. publication number 53-66279 to obtain according to JIS (Japanese Industrial Standards) P 8111.
Carrier 3 can contain the various adjuvants of suitably selecting in satisfying the scope of density of the present invention.The preferred embodiment of adjuvant includes, but not limited to brightener, conductive agent, filler, titanium dioxide, dry tenacity hardening agent, sizing agent, wet strength hardening agent, fixing agent, pH adjuvant and other adjuvant.The preferred embodiment of filler includes, but not limited to that lime carbonate, clay, porcelain earth, carclazyte (white earth), talcum, titanium, group are blue, pigment (as carbon black etc.), dyestuff, or the like.
Carrier can contain hydrophilic adhesive, metal oxide semiconductor (as alumina colloidal sol and titanium dioxide), antistatic agent (as carbon black etc.), and/or the face-coating or the back coating that are formed by these adjuvants, or two finishing coats.Particularly can use disclosed carrier among the Japanese unexamined patent publication No. publication number 63-220246.Heat when carrier 3 preferably tolerates fixedly, and satisfy brightness, sliding, frictional property, antistatic behaviour, the fixing requirement that is easy to cave in afterwards.
<toner image receiving layer 〉
Toner image receiving layer 2, be to be used to form the color toner of image and/or the acceptor of black toner, its function that has is: receive the toner-particle that comes from the intermediate transfer thin slice or develop drum by electricity or static in shifting print procedure, and use heat and pressure fixing toner image in fixation procedure.
Thermoplastic resin
Toner image receiving layer 2 contains thermoplastic resin.It this thermoplastic resin is had no particular limits, as long as can be out of shape under the temperature conditions of fixing toner image.Although in satisfying the scope of the object of the invention, can select different thermoplastic resins, preferably use and be used as the similar resin of toner binder.The thermoplastic resin of preferred toner image receiving layer 2 with through being usually used in the identical of toner binder, be vibrin or copolymer resin such as styrene or styrene-propene acid butyl ester, the perhaps preferably multipolymer of the multipolymer of styrene, styrene-propene acid butyl ester, cinnamic acrylic ester or the multipolymer of styrene-methacrylate.The toner image receiving layer preferably contains the thermoplastic resin greater than 20 weight %.
The preferred embodiment of the thermoplastic resin of toner image receiving layer 2 comprises, but be not limited to, (a) has the resin of ester bond, (b) urethane resin, (c) polyamide, (d) polysulfone resin, (e) Corvic, (f) polyvinyl butyral, (g) polycaprolactone resin and (h) polyolefin resin.
Specifically, (a) preferred embodiment with resin of ester bond comprises, but be not limited to, with dicarboxylic acid component (can by sulfonic acid group or carboxyl substituted) as terephthalic acid (TPA), m-phthalic acid, maleic acid, fumaric acid, phthalic acid, hexane diacid, decanedioic acid, azelaic acid, colophonic acid, succinic acid, benzenetricarboxylic acid, benzenetetracarboxylic acid and alkoxide component (can be replaced by hydroxyl) are as ethylene glycol, diethylene glycol, propylene glycol, bisphenol-A, the diester deriv of bisphenol-A (for example ethylene oxide adduct or propylene oxide adduct), bisphenol S, 2-ethyl cyclohexyl dimethanol, neopentyl glycol, the cyclohexyl dimethanol, glycerine, the vibrin that obtains during condensation; Polyacrylate resin or polymethacrylate resin such as polymethylmethacrylate, poly-n-butyl methacrylate, polymethyl acrylate, butyl polyacrylate; The polycarboxylate resin; Vinylite; The styrene-acrylate resin; Styrene-methacrylate co-polymer resin, toluene vinyl acrylate; Or the like.Example includes, but not limited to those disclosed among Japanese unexamined patent publication No. publication number 59-101395,60-294862,63-7971,63-7972 and the 63-7973 more specifically.
The vibrin of commercially available acquisition includes, but not limited to Vyron 103,200,280,290,300, GK-130 and GK-140 (being produced by Toyobo company limited); TafutonNE-382, U-5, ATR-2009 and ATR-2010 (producing) by Kao company limited; ElitelUE3500, UE3210 and XA-8153 (producing) by Unitika company limited; PolyesterTP-220 and R-188 (producing) by ippon synthetic chemical industry company limited; Deng.The acryl resin of commercially available acquisition comprises, but be not limited to Dianal SE-5437, SE-5102, SE-5377, SE-5649, SE-5466, SE-5482, HR-169, HR-124, HR-1127, HR-116, HR-113, HR-148, HR-131, HR-470, HR-634, HR-606, HR-607, LR-1065, LR-574, LR-143, LR-396, LR-637, LR-162, LR-469, LR-216, BR-50, BR-52, BR-60, BR-64, BR-73, BR-75, BR-77, BR-79, BR-80, BR-83, BR-85, BR-87, BR-88, BR-90, BR-93, BR-95, BR-100, BR-101, BR-102, BR-105, BR-106, BR-107, BR-108, BR-112, BR-113, BR-115, BR-116 and BR-117 (producing) by Mitsubishi Rayon company limited; Esrex P SE-0020, P SE-0040, P SE-0070, P SE-0100, P SE-01010 and P SE-1035 (producing) by Sekisui chemicals company limited; HymarST95 and ST120 (producing) by Sanyo chemicals Industrial Co., Ltd; FM601 (producing) by Mitsui chemicals company limited; Or the like.
The preferred embodiment that is used for (e) Corvic of toner image receiving layer 2 includes, but not limited to polyvinyl dichloride resin, vinyl chloride vinyl acetate copolymer resin, vinyl chloride-vinyl propionate ester copolymer resin, etc.
The preferred embodiment that is used for (f) polyvinyl butyral of toner image receiving layer 2 includes, but not limited to polyol resin, ethyl cellulose resin, celluosic resin such as cellulose acetate ester resin etc.The polyvinyl butyral of commercially available acquisition includes, but not limited to DenkaButyral 3000-1,40002,5000A and 6000C (being produced by Denki Kagaku Kogyo K.K.); Esrex BL-1, BL-2, BL-3, BL-S, BX-L, BM-1, BM-2, BM-5, BM-S, BH-3, BX-1 and BX-7 (producing) by Sekisui chemicals company limited; Or the like.These polyvinyl butyrals have the polyvinyl butyral content greater than 70 weight %, and average degree of polymerization preferably is higher than 500, more preferably are higher than 1000.
The preferred embodiment that is used for (g) polycaprolactone of toner image receiving layer 2 includes, but not limited to phenylethylene-maleic anhydride resin, polyacrylonitrile resin, polyether resin, epoxy resin, phenolics etc.
The preferred embodiment that is used for (h) polyolefin resin of toner image receiving layer 2 includes, but not limited to multipolymer, the acryl resin of polyvinyl resin, acrylic resin, alkene such as ethene and propylene and vinyl monomer, or the like.
These thermoplastic resins can use separately or two or more mix use.
The preferred thermoplastic resin that satisfies the required solid state properties of toner image receiving layer 2 itself that uses, the thermoplastic resin that perhaps two or more can be satisfied the required different solid state properties of toner image receiving layer 2 mix and use.
The thermoplastic resin that is preferred for toner image receiving layer 2 has the molecular weight greater than the thermoplastic resin that is used for toner.Yet according to the relation between the thermodynamic property of these two kinds of thermoplastic resins that are respectively applied for toner and toner image receiving layer 2, this relation of the molecular weight between them is always not preferred.For example, have at the thermoplastic resin that is used for toner image receiving layer 2 under the situation of the melt temperature that is higher than another, the resin that is used for toner image receiving layer 2 preferably has the molecular weight identical with another or greater than another molecular weight, this depends on environment.But the potpourri of the different thermoplastic resin of identical mean molecular weight is formed in also preferred use each other.The molecular weight that is used for the thermoplastic resin of toner is preferably determined according to the disclosed relation of Japanese unexamined patent publication No. publication number 8-334915.The molecular weight distribution of thermoplastic resin that is preferred for toner image receiving layer 2 is wideer than the molecular weight distribution of the thermoplastic resin that is used for toner.The solid state properties that is used for the thermoplastic resin of toner image receiving layer 2 must satisfy for example Japanese patent publication 5-127413 and Japanese unexamined patent publication No. publication number 8-194394,8-334915,8-334916,9-171265 and 10-221877 those disclosed.
The thermoplastic resin that is used for toner image receiving layer 2 is water type as water soluble resin or water-dispersed resin, reason following (i) and (ii):
(i) aqueous resins is not centrifugal in coating and dry run goes out organic solvent, so is having outstanding performance aspect environmental suitability and the processibility;
(ii) in many cases, release agent such as wax are at room temperature water-soluble hardly, just are dispersed in before usefulness in solvent such as water or the organic solvent.
This water-dispersion type thermoplastic resin is not only stable, and has good flexibility (adaptability) of operation.In addition, wet coating makes wax be easy to be seeped on the surface between coating and dry epoch, thus to release agent exert an influence (skew patience, bonding patience etc.).
This aqueous resins be not always formed, the constraint of key-structure, molecular geometry, molecular weight, molecular weight distribution etc., just requiring it is water-soluble type or water dispersible type.Hydrophilic or suction examples of groups includes, but not limited to sulfonic acid group, hydroxy-acid group, amino, acylamino-, ether group etc.
The preferred embodiment of water soluble resin includes, but not limited to Research Disclosure No.17,643 the 26th pages, No.18,716 the 651st pages, No.307, those disclosed among 105 873-874 pages or leaves and the Japanese unexamined patent publication No. publication number 64-13546.The particularly preferred example of water soluble resin comprises; but be not limited to vinyl pyrrolidone acetate copolymer, styrene-ethylene base pyrrolidone multipolymer, styrene maleic anhydride copolymer, water-soluble polyester, water soluble propene's acyl group, soluble polyurethane, water-soluble nylon, water-soluble epoxy resin etc.Gelatin is selected from the gelatin of lime treatment, the gelatin of acid treatment (the deliming gelatin that so-called lime content reduces).These gelatin can use separately or be used in combination with any.The gelatin of commercially available acquisition includes, but not limited to the gelatin (by Dainippon printing ink and chemical company production) of various types of Pluscoat (being produced by Gao chemicals Industrial Co., Ltd) and Fintex ES series, and they the two all be water-soluble polyester; The gelatin of Jurimar AT series (producing) by ippon fine chemicals company limited; Fintex 6161 and K-96 (by Dainippon printing ink and chemical company production); With Hyros NL-1189 and Hyros BH-997L (producing) by Seiko chemicals Industrial Co., Ltd; They all are water soluble propene's acyl groups.
The preferred embodiment of water-dispersed resin includes, but not limited to water-dispersed resin such as water dispersible acryl resin; Water-dispersible polyester, water dispersible polystyrene resin, water dispersible urethane resin, etc.; Emulsion such as emulsion acrylic resin, venamul, SBR (styrene butadiene ribber) emulsion, etc.; Above listed aqueous dispersion or the emulsion (resin, urethane resin, polyamide, polysulfone resin, Corvic, polyvinyl butyral, polycaprolactone resin and the polyolefin resin that promptly have ester bond) that is preferred for the thermoplastic resin of toner image receiving layer 2.Perhaps, can use the potpourri of two or more combinations of the top listed thermoplastic resin that is preferred for toner image receiving layer 2 or cation-modified resin.
The water-dispersed resin of commercially available acquisition comprises, but be not limited to, the resin of Vyronal series (producing) by Toyobo company limited, the resin of Pesuresin A series (producing) by Takamatsu grease company limited, the resin of Tafuton UE series (producing) by Kao company limited, the resin (producing) of resin of Polyester WR series (producing) and Eliel series by ippon synthesis of chemicals Industrial Co., Ltd by Unitika company limited, they all are polyester, and HyrosXE, the resin (being produced by ippon fine chemicals company limited) of resin of KE and PE series (being produced by Seiko chemicals Industrial Co., Ltd) and Jurimar ET series, they all are acryl resins.The melt-flow temperature (MET) of thin polymer film preferably is higher than prints reserve temperature (room temperature) before, and is higher than the temperature (100 ℃) that is used for fixing toner-particle.
The preferred use has the moisture thermoplastic resin fat liquor of self-dispersion type of following feature (1)-(4) as aforementioned thermoplastic resin.This is because the self-dispersion type emulsion does not contain surfactant, even it is little that the fusing point that therefore still has low hydroscopicity and cause because of moisture under the higher levels of humidity environment reduces, can suppress during the toner fixation procedure bonding failure to take place to take place between skew and/or the duration of storage thin slice.In addition, water type emulsion has outstanding environmental suitability and processibility.And, because this emulsion comprises the molecular structure that is easy to have higher cohesive energy, this emulsion keeps enough hardness in storage environment simultaneously, and in the toner fixation procedure of electrophotography, it is in molten condition, and present lower elasticity or viscosity, thereby form enough high-quality image by the toner-particle that is imbedded in the visual receiving layer.
(1) number-average molecular weight (Mn) 5000-10000 preferably is more preferably 5000-7000;
(2) molecular weight distribution (Mw/Mn), promptly the ratio of weight-average molecular weight and number-average molecular weight preferably is equal to or less than 4, more preferably is equal to or less than 3;
(3) glass temperature (Tg) is preferably 40-100 ℃, is more preferably 50-80 ℃; With
(4) volume average particle size 20-200nm φ preferably is more preferably 40-150nm φ.
Release agent
In order to prevent that toner image receiving layer 2 from causing skew, is mixed with release agent in the toner image receiving layer 2.Release agent is not subjected to the restriction of type, as long as its fusion under fixed temperature, and is separated on the surface of toner image receiving layer 2 unevenly and solidifies, and forms a releasing agent layer thus on toner image receiving layer 2.Example with this release agent of above-mentioned effect includes, but not limited to polysiloxane compound, fluoride, wax and deluster.Preferably use at least a or multiple following material that is selected from: silicone oil, Tissuemat E, Brazil wax, polysiloxane particle and polyethylene particle.
Specifically, disclosed polysiloxane compound, fluoride, the wax (except that natural wax) that is used for toner in disclosed compound and the following document in " Handbook of Silicon " that " Revised Edition:Property and Application of Wax " that comprising of can be used as that release agent uses, Koushobou published and Nikkan KogyoShinbun publish: Japanese Patent No. 2838498 and 2949558; Japanese patent application publication No. 59-38581 and 4-32380; Japanese unexamined patent publication No. publication number 50-117433,52-52640,57-148755,61-62056,61-62057,61-118760,2-42451,3-41465,4-212175,4-214570,4-263267,5-34966,5-119514,6-59502,6-161150,6-175396,6-219040,6-230600,6-295093,7-36210,7-43940,7-56387,7-56390,7-64335,7-199681,7-223362,7-287413,8-184992,8-227180,8-248671,8-2487799,8-248801,8-278663,9-152739,9-160278,9-185181,9-319139,9-319413,10-20549,10-48889,10-198069,10-207116,11-2917,11-449669,11-65156,11-73049 and 11-194542.These compounds can use separately also can two or more mix use.
The preferred embodiment of polysiloxane compound comprises, but be not limited to, (preferred embodiment of the unmodified silicone oil of commercially available acquisition comprises KF-96, KF-96L, KF-96H, KF-99, KF-50, KF-54, KF-56, KF-965, KF-968, KF-994, KF-995, HIVAC, F-4, the F-5 that is produced by Shinetsu chemicals Industrial Co., Ltd for unmodified silicone oil such as dimethicone oils, methyl hydrogen silicone oil, phenyl methyl silicone oil; SH200, SH203, SH490, SH510, SH550, SH710, SH704, SH705, SH7028A, SH7036, SM7060, SM7001, SM7706, SM7036, SH871107, SH8627 by the production of Toray Dow Corning polysiloxane company limited; TSF400 by the production of Toshiba polysiloxane company limited, TSF401, TSF404, TSF405, TSF431, TSF433, TSF434, TSF437, TSF450, TSF451, TSF456, TSF458, TSF483, TSF484, TSF4045, FSF4300, TSF4600, YF-33, YF-3057, YF-3800, YF-3802, YF-3804, YF-3807, YF-3897, YF-3905, XS69-A1753, TEX100, TEX101, TEX102, TEX103, TEX104, TSW831); (preferred embodiment of the amino modified silicone oil of commercially available acquisition comprises amino modified silicone oil, but be not limited to, KF-857, KF-858, KF-859, KF-861, KF-864 and KF-880 by the production of Shinetsu chemicals Industrial Co., Ltd, the SF8417 and the SM8709 that produce by Toray Dow Corning polysiloxane company limited, and TSF4700, the TSF4701, TSF4702, TSF4703, TSF4704, TSF4705, TSF4706, TEX150, TEX151 and the TEX154 that produce by Toshiba polysiloxane company limited); (preferred embodiment of the carboxy-modified silicone oil of commercially available acquisition comprises carboxy-modified silicone oil, but be not limited to, by the BY-16-880 of Toray DowCorning polysiloxane company limited production, by the TFS4770 and the XF42-A9248 of Toshiba polysiloxane company limited production); The silicone oil of methyl alcohol modification (preferred embodiment of the silicone oil of the methyl alcohol modification of commercially available acquisition includes, but not limited to the XF42-B0970 by the production of Toshiba polysiloxane company limited); The silicone oil of vinyl modification (preferred embodiment of the silicone oil of the vinyl modification of commercially available acquisition includes, but not limited to the XF40-A1987 by the production of Toshiba polysiloxane company limited); (preferred embodiment of the epoxide modified silicone oil of commercially available acquisition comprises epoxide modified silicone oil, but be not limited to, the SF8411 and the SF8413 that produce by Toray Dow Corning company limited, and TSF3965, the TSF4730, TSF4732, XF42-A4438, XF42-A5041, XC96-A4462, XC96-A4462, XC96-A4463, XC96-A4464 and the TEX170 that produce by Toshiba polysiloxane company limited); (the polyether-modified silicone oil of commercially available acquisition comprises polyether-modified silicone oil, but be not limited to, KF-351 (A) by the production of Shinetsu chemicals Industrial Co., Ltd, KF-352 (A), KF-353 (A), KF-354 (A), KF-355 (A), KF-615 (A), KF-618 (A) and KF-945 (A), SH3746 by the production of Toray Dow Corning polysiloxane company limited, SH3771, SH8421, SH8419, SH8400 and SH8410, and the TSF4440 that produces by Toshiba polysiloxane company limited, TSF4441, TSF4445, TSF4446, TSF4450, TSF4452, TSF4453 and TSF4460); The silicone oil of silanol modification; The silicone oil of methacryl modification; Sulfhydryl modified silicone oil; (silicone oil of the pure modification of commercially available acquisition comprises the silicone oil of alcohol modification, but be not limited to, by the SF8427 and the SF8428 of Toray Dow Corning polysiloxane company limited production, by TSF4750, TSF4751 and the XF42-B0970 of Toshiba polysiloxane company limited production); (the alkyl-modified silicone oil of commercially available acquisition comprises alkyl-modified silicone oil, but be not limited to, the SF8416 that produces by Toray Dow Corning polysiloxane company limited, and TSF410, the TSF411, TSF4420, TSF4421, TSF4422, TSF4450, XF42-334, XF42-A3160 and the XF42-A3161 that produce by Toshiba polysiloxane company limited); The silicone oil of fluorine modification (silicone oil of the fluorine modification of commercially available acquisition includes, but not limited to the SF1265 that produced by Toray Dow Corning polysiloxane company limited, and the FQF502 that is produced by Toshiba polysiloxane company limited); (polysiloxane rubber of commercially available acquisition or polysiloxane particulate comprise for polysiloxane rubber or polysiloxane particulate, but be not limited to, by SH851U, SH745U, SH55UA, SE4705U, the SH502UA﹠amp of Toray Dow Corning polysiloxane company limited production; B, SRX539U, SE6770-P, DY38-038, DY38-047, Trefil F-201, F-202, F-250, R-900, R902A, E-500, E-600, E-601, E-506 and BY29-119, and the Tospal 105,120,130,145,250 and 3120 that produces by Toshiba polysiloxane company limited); (the polysiloxane-modified resin of commercially available acquisition comprises the polysiloxane-modified compound of the multipolymer of polysiloxane-modified resin such as olefin resin, vibrin, vinylite, polyamide, celluosic resin, phenoxy resin, vinyl chloride-vinyl acetate resin, urethane resin, acryl resin, styrene-propene acid resin and these resins, but be not limited to, by Dainichiseika Color ﹠amp; The Dialoma SP203 that Chemicals Mfg. company limited produces, SP712, SP2105 and SP2023, Modipa FS700 by the production of ippon grease company limited, FS710, FS720, FS730 and FS770, Saimack US-270 by the production of Toa Gosei chemicals Industrial Co., Ltd, US-350, US-352, US-380, US-413, US-450, Rezata GP-705, GS-30, GF-150 and GF-300, SH997 by the production of Toray Dow Corning polysiloxane company limited, SR2114, SH2104, SR2115, SR2202, DCI-2577, SR2317, SE4001U, SRX625B, SRX643, SRX439U, SRX488U, SH804, SH840, SR2107 and SR2115, and the YR3370 that produces by Toshiba polysiloxane company limited, TSR1122, TSR102, TSR108, TSR116, TSR117, TSR125A, TSR127B, TSR144, TSR180, TSR187, YR47, YR3187, YR3224, YR3232, YR3270, YR3286, YR3340, YR3365, TEX152, TEX153, TEX171 and TEX172); Reactive polysiloxane composition such as addition reaction type polysiloxane composition, (the reactive polysiloxane compound of commercially available acquisition comprises for peroxide curing type and ultraviolet hardening, but be not limited to, by the TSR1500 of Toshiba polysiloxane company limited production, TSR1510, TSR1511, TSR1515, TSR1520, YR3286, YR3340, PSA6574, TPR6500, TPR6501, TPR6600, TPR6702, TPR6604, TPR6701, TPR6705, TPR6707, TPR6708, TPR6710, TPR6712, TPR6721, TPR6722, UV9315, UV9425, UV9430, XS56-A2775, XS56-A2982, XS56-A3075, XS56-A3969, XS56-A5730, XS56-A8012, XS56-B1794, SL6100, SM3000, SM3030, SM3200 and YSR3022).
The preferred embodiment of fluorine compounds comprises, but be not limited to, (fluorocarbon oil of commercially available acquisition comprises fluorocarbon oil, but be not limited to, Dyfloyl#1 by the production of Daikin Kogyo company limited, #3, #10, #0, #50, #100, Unidyn TG-440, TG-440, TG-452, TG-490, TG-560, TG-561, TG-590, TG-652, TG-670U, TG-991, TG-999, TG-3010, TG-3020 and TG-3510, MF-100 by the production of Tokem Products Co., Ltd, MF-110, MF-120, MF-130, MF-160 and MF-160E, Surflon S-111 by the production of Asahi Glass Co., Ltd., S-112, S-113, S-121, S-131, S-132, S-141 and S-145, and the FC-430 and the FC431 that produce by Mitsui Phluoro chemicals company limited); Fluororubber (fluororubber of commercially available acquisition includes, but not limited to the LS63U by the production of Toray Dow Corning polysiloxane company limited); (the fluorine modified resins of commercially available acquisition includes, but not limited to Modipa F200, F220, F600, F2020 and the F3035 by the production of ippon grease company limited to the fluorine modified resins, by DainichiseikaColor ﹠amp; Dialoma FF203 and FF204 that Chemicals Mfg. company limited produces, Surflon S-381, S-383, S-393, SC-101, SC-105, KH-40 and SA-100 by the production of Asahi Glass Co., Ltd., and EF-351, the EF-352, EF-801, EF-802, EF-601, TFE, TFEMA and the PDFOH that produce by Tokem Products Co., Ltd, the THV-200P that produces by Sumitomo 3M company limited); (the fluoro sulfonate examples for compounds of commercially available acquisition comprises the fluoro sulfonate compound, but be not limited to, by EF-101, EF-102, EF-103, EF-104, EF-105, EF-112, EF-121, EF122A, EF122B, EF-122C, EF-123A, EF-123B, EF-125M, EF-132, EF-135M, EF-305, FBSA, KFBS and the LFBS of Tokem Products Co., Ltd production); Fluosulfonic acid; Fluoride (for example, anhydrous hydrofluoric acid, diluted hydrofluoric acid, fluoboric acid, zinc fluoroborate, nickel fluoborate, tin fluoborate, lead fluoborate, cupric fluoborate, hydrofluosillicic acid, fluoridize potassium titanate, perfluoro caprylic acid, perfluorooctanoic acid etc.); And inorganic fluoride (for example aluminum fluoride, potassium silicofluoride, fluoridize potassium zirconium, zinc fluoride tetrahydrate, potassium fluoride, lithium fluoride, barium fluoride, tin fluoride, potassium fluoride, acid potassium fluoride, magnesium fluoride, titanium fluoride, ammonium hexafluorophosphate, Potassium Hexafluorophosphate etc.).
The preferred embodiment of wax includes, but not limited to paraffin, Synthin, modified waxes, wax oil (hydrowax), natural wax etc.
The preferred embodiment of the paraffin of commercially available acquisition comprises, but be not limited to, by Paraffin Wax 155,150,140,135,130,125,120,115, NHP-3, NHP-5, NHP-9, NHP-10, NHP-11, NHP-12, NHP-15G, SP-0160, SP-0145, SP-1040, SP-1035, SP-3040, SP-3035, NPS-8070, NPS-L-70, OX-2151, OX2251, EMUSTAR-0384 and the EMUSTAR-0136 of Nippon Seiro company limited production; Serozole 686,651-A, A, H-803, B-460, E-172,866, K-133, Hidrin D-337 and E-139 by the production of Chukyo grease company limited; And 125 ° of Paraffin that produce by Nisseki Mitsubishi oil company limited, 125 P, 130 ° of Paraffin, 135 ° of Paraffin, 135 ° of H, 140 ° of Paraffin, 140 ° of N, 145 ° of Paraffin and Paraffin Wax M; Microcrystalline wax, Hi-Mic-2095, Hi-Mic-3090, Hi-Mic-1080, Hi-Mic-1070, Hi-Mic-2065, Hi-Mic-1045, Hi-Mic-2045, EMUSTAR-0001 and the EMUSTRAR-042X that produces by Nippon Seiro company limited for example, by the Serozole 967 and the M of Chukyo grease company limited production, by the 155Microwax and the 180Microwax of Nisseki Mitsubishi oil company limited production; And vaseline, for example OX-1749, OX-0450, OX-0650B, OX-0153, OX-261BN, OX-0851, OX-0550, OX-0750B, JP-1500, JP-056R and the JP-011P that produces by NipponSeiro company limited.
The preferred embodiment of the synthetic hydrocarbon of commercially available acquisition comprises, but be not limited to, Tissuemat E, the Polyron A that produces by Chukyo grease company limited, 393 and H-481 for example, and Sunwax E-310, the E-330, E-250P, LEL-250, LEL-800 and the LEL-400P that produce by Sanyo chemicals Industrial Co., Ltd; Polypropylene wax, for example Viscol 330-P, 550-P and the 660-P that produces by Sanyo chemicals Industrial Co., Ltd; Fischer-Tropsch wax, for example FT-100 and the FT0070 that produces by Nippon Seiro company limited; And amide compound or acid imide compound, for example acylamino-stearate, acylimino phthalic anhydride etc. (for example Serozole 920, B-495, HimicronG-270, G-110 and the Hidrin 757 that produces by Chukyo grease company limited).
The preferred embodiment of modified waxes includes, but not limited to the QN-7700 of polypropylene as being produced by Sanyo chemicals Industrial Co., Ltd of amine modification, acrylic acid modified wax; The wax of fluorine modification; Olefin-modified wax; NPS-6010 and the HAD-5090 of the wax of urethane modification as producing by Nippon Seiro company limited; And NPS-9210, NPS-9215, OX-1949 and the XO-020T of pure wax as producing by Nippon Seiro company limited.
The preferred embodiment of wax oil includes, but not limited to castor bean or castor oil, for example the Castor Wax that is produced by Ito Oil production company limited; Castor oil derivative, for example the dehydrated castor oil DCO that produces by Ito Oil production company limited, DCO Z-1, DCO-Z2, Castor Oil Fatty Acid CO-FA, castor oil acid, dehydrated castor oil fatty acid DCO-FA, dehydrated castor oil fatty acid epoxy-ester D-4 ester, castor oil urethane acrylate CA-10, CA-20, CA-30, castor oil derivative MINERASOL S-74, S-80, S-203, S-42X, RC-17, RC-55, RC-335, specific castor oil condensation fatty acid MINERALSOL RC-2, RC-17, RC-55, RC-335, specific castor oil condensation fatty acid ester MINERALSOL LB-601, LB-603, LB-604, LB-7-2, LB-7-3, #11 and L164; Stearic acid, for example the 12-hydroxy stearic acid of producing by Ito Oil production company limited; Lauric acid; Myristic acid; Palmitic acid, docosanoic acid; The decanedioic acid of producing by Ito Oil production company limited for example; The undecenoic acid of producing by Ito Oil production company limited for example; The enanthic acid of producing by Ito Oil production company limited for example; Maleic acid; Senior Malaysia oil, for example HIMALEIN DC-15, LN-10, OO-15, DF-20 and the SF-20 that produces by Ito Oil production company limited; Blown oil, for example Serbonol#10, #30, #60, R-40 and the S-7 that produces by Ito Oil production company limited; And cyclopentadiene oil, for example CP Oil and the CPOil-S that produces by Ito Oil production company limited.
The preferred embodiment of natural wax includes, but not limited to vegetable wax, animal wax and mineral wax.It is desirable to plant source in these natural waxs.Be used at moisture thermoplastic resin considering compatibility under the situation of toner image receiving layer 2, more preferably use the water dispersible natural wax.
The preferred embodiment of vegetable wax includes, but not limited to the EMUSTAR-0413 of Brazil wax such as the production of Ito Oil production company limited and the Serozole 524 that Chukyo grease company limited produces; Castor oil, rapeseed oil that Ito Oil production company limited produces; Soybean oil, sumac wax, cotton wax, rice wax, sugarcane wax, candelila wax, Japan tallow and jojoba oil also can use animal wax such as beeswax, sheep oil, spermaceti, whale oil and lanocerin.The preferred especially Brazil wax that uses melt temperature in these plants are cured with 70-95 ℃, because it has the toughness that excellent skew patience, bonding patience, penetration capacity, reflecting feel, cracking resistance are opened, and the electrophotographic image that can form high quality image receives thin slice.
The preferred embodiment of mineral wax includes, but not limited to natural wax such as montan wax, brown coal ester type waxes, ceresine, paraffin etc.; Fatty acid ester is as can be by Chukyo grease company limited commercially available Sensosizer DOA, AN-800, DINA, DIDA, DOZ, DOS, TOTM, TITM, E-PS, nE-PS, E-PO, E-4030, E-6000, E-2000H, E-9000H, TCP and C-1100; Synthin, comprise Tissuemat E as the Polyron A that produces by Chukyo grease company limited, 393 and H-481, and Sunwax E-310, the E-330, E-250P, LEL-250, LEL-800 and the LEL-400P that produce by Sanyo chemicals Industrial Co., Ltd; With Viscol 330-P, 550-P and the 660-P of polypropylene wax as producing by Sanyo chemicals Industrial Co., Ltd.The wherein preferred especially montan wax that uses the melt temperature with 70-95 ℃, because it has the toughness that excellent skew patience, bonding patience, penetration capacity, reflecting feel, cracking resistance are opened, and the electrophotographic image that can form high quality image receives thin slice.
The natural wax content of toner image receiving layer 2 is 0.1-4g/m preferably
2, be more preferably 0.2-2g/m
2If natural wax content surpasses 0.1g/m
2, particularly be offset patience and bonding patience will significantly reduce.In other words, if natural wax content surpasses 4g/m
2, just can not provide image to receive thin slice with high quality image.Preferred single natural wax of planting has preferred 70-95 ℃, more preferably 75-90 ℃ melt temperature.
The preferred embodiment of deluster includes, but not limited to inorganic and organic deluster of solid particulate form.Inorganic deluster comprises oxide such as silicon dioxide, titanium dioxide, magnesium oxide, aluminium oxide etc.; Alkali salt such as barium sulphate, lime carbonate, magnesium sulphate etc.; With silver halide such as silver chloride, silver bromide etc.Particularly in following patent, provided a large amount of alternative organic delusters: as Deutsches Reichs-Patent 2529321, BrP 760775 and 1260772 and United States Patent (USP) 1201905,2192241,3053662,3062649,3257206,3322555,3353958,3370951,3411907,3437484,3523022,3615554,3635714,3769020,4021245 and 4029504 described in.
The preferred embodiment of deluster material includes, but not limited to starch, cellulose esters (for example cellulose acetate propionate), cellulose ether (for example ethyl cellulose) and synthetic resin.Synthetic resin is preferably non-water-soluble.This synthetic resin comprises, but be not limited to polyacrylic acid or polymethacrylate (polyalkyl acrylate for example, polyalkyl methacrylate, polyacrylic acid alkoxy alkyl or polyacrylic acid methyl alkoxy Arrcostab, polyacrylic acid ethylene oxidic ester or polyacrylic acid methyl ethylene oxidic ester), polyacrylamide, PMAm, polyvinylesters (for example polyvinyl acetate), polyacrylonitrile, polyolefin (for example tygon), polystyrene, benzoguanamine resin, the polymkeric substance of formaldehyde condensation, epoxy resin, polyamide, polycarbonate, phenolics, polyvinylcarbazole and polyvinyl dichloride.Can utilize and contain the polymer of monomers that is useful on above-mentioned polymkeric substance.
Utilizing under the situation of multipolymer, polymkeric substance can contain a spot of hydrophilic monomeric units.Perhaps, this multipolymer can be a kind of in atactic polymers, block polymer and the graft polymer, and they contain a hydrophilic monomer separately.The preferred embodiment that forms the monomer of hydrophilic repetitive comprises, but be not limited to, acrylic acid, methacrylic acid, α-, beta-unsaturated carboxylic acid, acrylic acid hydroxyalkyl acrylate, methacrylic acid hydroxyl Arrcostab, acrylic acid sulfo group Arrcostab, methacrylic acid sulfo group Arrcostab and styrene sulfonate.
Particularly, there is the organic deluster that can obtain described in a large amount of following documents: BrP 1055713, United States Patent (USP) 1939213,2221873,2268662,2322037,2376005,2391181,2701245,2992101,3079257,3262782,3443946,3516832,3539344,3591397,3754924 and 2767448, and Japanese unexamined patent publication No. publication number 49-106821 and 57-14835.These solid particles can use separately or use with two or more combination in any.Mean grain size is 1-100 μ m preferably, is more preferably 4-30 μ m.The use amount of solid particle is 0.01-0.5g/m aptly
2, be more preferably 0.02-0.3g/m
2
The release agent that joins the toner image receiving layer can be derivant, compound, refined products or the potpourri of above-mentioned material.In addition, consider the compatibility of the moisture thermoplastic resin that is used for toner image receiving layer 2, release agent is preferably water miscible.Preferred toner image receiving layer 2 has preferred 0.1-10 weight %, more preferably 0.3-8.0 weight %, most preferably the release agent content of 0.5-5.0 weight %.
Other component material
In order to improve the thermodynamic property of toner image receiving layer 2, can add various other component materials therein.The preferred embodiment of other component material includes, but not limited to colorant, plastifier, filler, crosslinking chemical, antistatic controlling agent, emulsifying agent, spreading agent etc.Consider toner image fixing during the importance of thermal conductivity (low thermal conductivity) of toner image receiving layer 2, this component material is hollow particle preferably.
--colorant--
Colorant comprises brightener, Chinese white, colored pigment, dyestuff etc.
Brightener be in ultraviolet environs and the fluorescence scope of 400-500nm in have receptivity compound.Conventional fluorescent colorant can use under the situation that is not subjected to the particular type restriction.The preferred embodiment of brightener includes, but not limited to disclosed compound in " The Chemistry of Synthetic Dyes " the 8th volume the 8th chapter that K.VeenRatarman edits.Specifically, this compound comprises diphenyl ethene compounds, coumarin compound, biphenol compound, benzoxazol quinoline compound, naphthalimide compound, pyrazoline compounds, hydroxyquinoline compounds etc.The preferred embodiment of the brightener of commercially available acquisition includes, but not limited to the White Fulfa PSN, PHR, HCS, PCS and the B that are produced by Sumitomo chemicals company limited, and the UVITEX-OB that is produced by Chiba-Geigy company limited.
Chinese white includes, but not limited to other inorganic pigment that titanium dioxide, lime carbonate etc. and back are described about filler.
The preferred embodiment of colored pigment comprises, but be not limited to various pigment and for example disclosed AZO pigments such as azo lake pigment (for example carmine 6B, red 2B) among the Japanese unexamined patent publication No. publication number 63-44653, insoluble azo colour (for example an azophosphine, two azophosphines, pyrazoles orange and Balkan (Vulcan) orange), condensed azo pigment (for example chromophthal is yellow red in chromophthal); Many ring pigment (for example phthalocyanine covellite and phthalocyanine verdigris), two piperazines encircle that pigment (for example two piperazine purples), indolone encircle pigment (for example indolone Huang) more, slen encircles pigment (perylene, perynon, flavanthrone, thioindigo) more more; Mordant pigment (for example peacock green, rhodamine B, rhodamine G and Victoria Blue B); With inorganic pigment such as oxide, titania, colcother, sulfate (for example precipitable barium sulphate), carbonate (precipitable lime carbonate), silicate (for example hydrosilicate and anhydrous silicate), metal powder (for example aluminium powder, bronze powder, blue powder), carbon black, chrome yellow, barba hispanica etc.
These Chinese whites can use separately or can two or more be used in combination.Wherein titanium dioxide is most preferred pigment.
This pigment is not subjected to the specific limited of shape, yet, consider the importance of the thermal conductivity (low thermal conductivity) of toner image during fixing to preferably include hollow particle.
Various dyestuffs as colorant comprise oil-soluble dyes such as anthraquinone compounds and azo-compound.
The particularly preferred example of dyestuff comprises, but be not limited to, reducing dye such as C.I. Vat Violet 1, C.I. reduction purple 2, C.I. reduction purple 9, C.I. Vat Violet 13, C.I. reduction purple 21, C.I. vat blue 1, C.I. vat blue 3, C.I. Vat blue 4, C.I. reductive blue 6, C.I. vat blue 14, C.I. vat blue 20, C.I. vat blue 35, disperse dyes such as C.I. disperse violet 1, C.I. disperse violet 4, C.I. disperse violet 10, C.I. disperse blue 3, C.I. disperse blue 7, C.I. disperse blue 58 and oil-soluble dyes such as C.I. solvent violet 13, C.I. solvent violet 14, C.I. solvent violet 21, C.I. solvent violet 27, C.I. solvent blue 19 1, C.I. solvent blue 19 2, C.I. solvent blue 25, C.I. solvent blue 55.Can preferably use the coloured coupling agent that is used for silver-colored photography.
Toner image receiving layer 2 preferably contains 0.1-8g/m
2, more preferably 0.5-5g/m
2Colorant.If colorant content is less than lower limit 0.1g/m
2, the transmittance of toner image receiving layer 2 increases.On the other hand, if colorant content surpasses upper limit 8g/m
2, toner image receiving layer 2 property handled, loose bonding patience and/or cracking resistance are held toughness meeting variation.
--plastifier--
The various conventional plastifier that is used for resin can use under the situation without any specific limited.Plastifier has control toner image layer 2 because of the heat that applies in the toner fixation procedure and/or pressure drifts about or the function of softening or fusion.This plastifier can be selected by consulting following books: " Handbook of Chemistry ", and Chemical Society of Japan is published by Maruzen; " Plasticizer-Theory and Applications-" Kouichi Murai is published by Koushobou; " Study On Plasticizer Vol.1 " and " Study OnPlasticizer Vol.2 " Polymer Chemistry Association; " HandbookRubberPlastics Compounding Chemicals " Rubber Digest Ltd. etc.
Utilizable plastifier, quote as proof on the one hand and be high boiling organic solvent or hot solvent, on the other hand institute's illustration among Japanese unexamined patent publication No. publication number 59-83154,59-178453,59-178454,59-178455,59-178457,62-174745,62-245253,61-09444,61-2000538,62-8145,62-9348,62-30247,62-136646 and the 2-235694 for example.The example of disclosed plastifier comprises ester such as phthalic ester, phosphate, fatty ester, rosin ester, adipate, sebacate, azelate, benzoic ether, butyric ester, epoxidation fatty ester, oxyacetate, propionic ester, benzenetricarboxylic acid ester, citrate, sulphonic acid ester, carboxylate, succinate, maleate, phthalic ester, stearate in these publications; Acid amides such as fatty acid amide, sulfonamide; Ether; Alcohol; Lactone; And polyoxyethylene.
Using under the situation of polymkeric substance as plastifier, the molecular weight of polymkeric substance is preferably less than the molecular weight of the adhesive resin for the treatment of plasticising.Specifically, the molecular weight of this plastifier is more preferably less than 5000 preferably less than 15000.Using under the situation of polymkeric substance as plastifier, the type of plastifier polymkeric substance is preferably identical with the adhesive resin for the treatment of plasticising.For example, when the plasticized polyesters resin, the preferred use has low-molecular-weight polyester.Equally, oligomer can be used for plastifier.
The preferred embodiment of the plastifier of the commercially available acquisition except aforesaid compound includes, but not limited to Adecasizer PN-170 and the PN-1430 that Asahi Denka Kogyo K.K. produces; PARAPLEX-G-25, G-30 and G-40 that HALL company produces; Estergum 8L-JA, Ester R-95, Pentaryn 4851, FK115, FK4820, FK830, Ruizol 28-JA, Picorastic A75, Picotex LC and Crystalex 3085 that RikaHercules company limited produces.
In order to reduce, can use plastifier arbitrarily because of toner-particle is imbedded in the stress that produces in the toner image receiving layer 2 and tension force (physics tension force that causes because of elastic force and/or viscosity or the stress that causes because of the mass balance of molecule, main chain and side chain).Plastifier can Micro Disperse State be present in the toner image receiving layer 2, is present in the zone (similar island shape) that is separated with the micron size, perhaps mixes with other component such as bonding agent also fully to be dissolved in wherein.
Toner image receiving layer 2 preferably has 0.001-90 weight %, more preferably 0.1-60 weight %, the most preferably plastifier of 1-40 weight %.
Can use plastifier to realize that skew (toner layer separates with fixed area), crimping balance and the electrophotographic image of slip ability (improving the slip dirigibility owing to reducing friction force), fixed area receive antistatic behaviour (accumulation of the electrostatic toner image) optimization of thin slice 1.
--filler--
Can use organic filler and inorganic filler or pigment, for example those are known as those of rigidizer, filler and hardening agent of adhesive resin.
" the Filler Handbook " that can consult " New Edition Plastic CompoundingAgent Basics And Applications ", the Taiseisha of " Handbook RubberPlastics Compounding Chemicals " Rubber Digest Ltd. etc., Taiseisha waits and selects filler.
The inorganic pigment that can obtain comprises, but be not limited to silicon dioxide, alumina, titania, zinc paste, zirconia, mica shape iron oxide, zinc white, massicot, cobalt oxide, strontium chromate, molybdenum pigment, smectite, magnesium oxide, calcium oxide, lime carbonate, mullite.Preferred especially silicon dioxide or alumina are as filler.These pigment can use separately or mix use with two or more.Filler preferably includes particulate.If particle diameter is big, toner image receiving layer 2 is easy to have rough surface.
The silicon dioxide that can obtain has two kinds, i.e. preparing spherical SiO 2 and amorphous silica.These silicon dioxide can wet method or dry method or, synthetic with aerosol processing.The hydrophobic silica particle can be handled with trimethyl silyl or silicon.In this case, preferably use the silicon dioxide colloid particle.This silicon dioxide preferably has the mean grain size of 200-5000nm.
Silica dioxide granule is porous preferably also.The porous silica particle preferably has 4-120nm, more preferably average pore volume/unit mass of the mean grain size of 4-90nm and 0.5-3ml/g.
Two kinds of alternative alumina are arranged, promptly do not have diaspore and alumina hydrate.No diaspore can be the crystal form of α, β, γ, δ, ζ, η, θ, κ, ρ or χ.The no diaspore of preferred use, rather than use the alumina hydrate.Monohydrate comprises pseudobochmite, boehmite and diaspore.Trihydrate comprises gibbsite and bayerite.Alumina particle preferably has 4-300nm, more preferably the mean grain size of 4-200nm.Alumina particle is porous preferably also.The porous alumina particle preferably has the mean grain size of 50-500nm and average pore volume/unit mass of 0.3-3ml/g.
The alumina hydrate can aluminum solutions precipitates the sol-gel process of alumina or the method for hydrolysis basic aluminate is synthesized by ammoniacal liquor is added.No diaspore can obtain by the dehydration of heating alumina hydrate.
Add the dry mass of the adhesive phase of filler relatively, filer content is 5-2000 weight % preferably.
--crosslinking chemical--
In order to make toner image receiving layer 2 have storage-stable and to control the thermoplasticity of toner image receiving layer 2, sneak into crosslinking chemical therein.Have two above reactive groups in the molecule as the compound of this class crosslinking chemical, these groups are epoxide group, isocyanate group, aldehyde radical, active halogens, active methylene group, ethinyl and well known to a person skilled in the art other group for example.Perhaps, use the compound with two above groups effectively, described plural group can pass through ionic bonding, hydrogen bonding, coordination bonding etc. and form a key.
Crosslinking chemical includes, but not limited to known composition as resin coupling agent, rigidizer, polymerization initiator, polymerization accelerant, coagulator, film forming agent, film forming assistant agent etc.The preferred embodiment of coupling agent comprises, but be not limited to those disclosed among chlorosilane, vinyl silanes, epoxy silane, amino silane, aluminum alkoxide chelate, titanate coupling agent and " Handbook RubberPlasticsCompounding Chemicals " Rubber Digest Ltd..
--antistatic controlling agent--
Toner image receiving layer 2 preferably contains antistatic controlling agent, so that the transfer of control toner and bonding, and prevent that toner image receiving layer 2 is antistatic and bonding.The example of conventional known antistatic controlling agent includes, but not limited to surfactant such as cationic surfactant, anionic surfactant, amphoteric surfactant or non-ionic surfactant, polyelectrolyte and conducting metal oxide.The instantiation of antistatic controlling agent comprises, but be not limited to, cationic antistatic agent such as quaternary ammonium salt, polyamine derivatives, cation-modified polymethylmethacrylate or cation-modified polystyrene, anionic antistatic agents such as alkylphosphonic or anionic polymer and non-ionic antistatic agent such as fatty ester or polyoxyethylene.Under the electronegative situation of toner, the antistatic controlling agent that mixes with toner image receiving layer 2 is cationic antistatic agent or non-ionic antistatic agent preferably.
The preferred embodiment of conducting metal oxide includes, but not limited to ZnO, TiO
2, SnO
2, Al
2O
3, In
2O
3, SiO
2, MgO, BaO, MoO
3Deng.These conducting metal oxides can use separately or form that can composite oxides is used.This metal oxide can also be mixed with assorted element.For example, ZnO can be mixed with Al or In, TiO
2Can be mixed with Nb or Ta, and SnO
2Can be mixed with Sb, Nb or halogen.
--other adjuvant--
Improve imaging stability and the optics of itself and the stability of physical characteristics, can in toner image receiving layer 2, add various other adjuvants.The adjuvant of realizing this purpose comprises antioxidant, antiaging agent, anti-disrupting agent, antiozonant, ultraviolet light absorber, metal complex, light stabilizer, antiseptic, mildewproof agent etc.
The preferred embodiment of antioxidant comprises, but be not limited to, benzodihydropyran composition, benzofuran compound, oxybenzene compound (for example hindered phenol), hydroquinone derivatives, hindered amine derivant, spiral indane (spiroindan) compound also have those disclosed among the Japanese unexamined patent publication No. publication number 61-159644 in addition.
Antiaging agent can be consulted " Handbook RubberPlastics CompoundingChemicals-the 2nd edition " (Rubber Digest Ltd. published in 1993) 76-121 page or leaf and select.
The preferred embodiment of ultraviolet light absorber comprises, but be not limited to, U.S. Patent number 3,533, disclosed ultraviolet ray absorbing polymer among disclosed 4-thiazolidinone compound and the Japanese unexamined patent publication No. publication number 62-260152 among disclosed benzotriazole, the Japanese unexamined patent publication No. publication number 46-2784 in 794.The preferred embodiment of metal complex includes, but not limited to U.S. Patent number 4,241, and 155,4,245,018 and 4,254,195, those disclosed among Japanese unexamined patent publication No. publication number 61-88256,62-174741,63-199248,1-75568 and the 1-74272.Metal complex can be selected from disclosed light stabilizer in ultraviolet light absorber and " Handbook RubberPlastics Compounding Chemicals-the 2nd edition " 76-121 page or leaf (Rubber Digest Ltd. published in 1993).The material that can be used for toner image receiving layer 2 is the known adjuvant of conventional photographic art.For example, disclosed various adjuvants in the 17643rd phase of Research Disclosure magazine (RD) (in Dec, 1987), the 18716th phase (in November, 1979) and the 307105th phase (in November, 1989), as shown in the table:
Adjuvant | RD17643 | RD18716 | RD307105 |
Brightener | 24 | 648R | 868 |
Stabilizing agent | 24-25 | 649R | 868-870 |
Light absorber (UV absorbing agent) | 25-26 | 649R | 873 |
The color image stabilizing agent | 25 | 650R | 872 |
Film hardener | 26 | 651L | 874-875 |
Bonding agent | 26 | 651L | 873-874 |
Plastifier/lubricant | 27 | 650R | 876 |
Coating assistant agent (surfactant) | 26-27 | 650R | 875-876 |
Antistatic agent | 27 | 650R | 976-977 |
Deluster | | | 878-879 |
Toner image receiving layer 2 is to form by using the cable coating machine that one coating fluid that contains polymkeric substance is coated on the carrier 3 and is dried.Coating fluid is by with adjuvant such as thermoplastic polymer and plastifier dissolving or evenly spread in an organic solvent such as alcohol or the ketone and make.The preferred embodiment of organic solvent includes, but not limited to methyl alcohol, isopropyl alcohol and methyl ethyl ketone.Using water-soluble polymers to be used under the situation of toner image receiving layer 2, toner image receiving layer 2 can be coated to by the aqueous solution with polymkeric substance on the carrier 3 and form.Under the situation of using non-soluble polymer, toner image receiving layer 2 can be coated to by the water dispersible solution with polymkeric substance on the carrier 3 and form.
Coating temperature when polymeric layer forms preferably is higher than the reserve temperature (room temperature) before printing, and is lower than toner fixed temperature (100 ℃).
Coating toner image receiving layer 2 is so that obtain preferred 1-20g/m
2, more preferably 4-15g/m
2Dry weight and preferred 1-30 μ m, the more preferably thickness of preferred 2-20 μ m.
<electrophotographic image receives the solid state properties of thin slice 〉
Following description will be referred to the solid state properties that electrophotographic image receives thin slice 1.The known surface free energy or the contact angle that can pass through the surface of mensuration heating and cooling front and back toner image receiving layer 2, estimate the release agent that is scattered in the toner image receiving layer 2 and whether transfer on the surface, and form releasing agent layer or film from the teeth outwards because of melted by heating.
The surface free energy of toner image receiving layer
When the polarity part difference of the surface free energy of toner image receiving layer was big before the heating and after heating and the cooling, this difference can make release agent transfer on the surface of toner image receiving layer.This fact shows and forms a releasing agent layer from the teeth outwards.This be since can bonding two kinds of materials or with one what separate with another is the surface free energy of material, its polarity part especially.In general, we can say that the surface free energy of material is more little, material is bonding poor more.
Particularly, with γ sp
0[mJ/m
2] and γ sp
1[mJ/m
2] respectively as add thermal pattern receive the surface free energy polarity part of toner image receiving layer before the thin slice value and with image receive thin slice be heated to 120 ℃ then it is cooled to 25 ℃ after the values of surface free energy polarity part of toner image receiving layer, meet the following conditions:
γsp
0-γsp
1≥2.5[mJ/m
2]
The difference of this surface free energy approximates or greater than 3[mJ/m
2].
In this case, the value (γ sp) of the polarity of surface free energy part can toner image receiving layer and the surperficial relative liquid i of fixed band and the contact angle (θ of j
iAnd θ
j) be that the basis uses following Fowks ' formula to obtain:
γ wherein
LiAnd γ
LjRepresent tension force intrinsic among liquid i and the j respectively;
γ
d LiAnd γ
d LjRepresent capillary dispersancy part intrinsic among liquid i and the j respectively;
γ
p LiAnd γ
p LjRepresent capillary polarity part intrinsic among liquid i and the j respectively;
θ
iAnd θ
jRepresent the contact angle of liquid i and j respectively;
The contact angle of toner image receiving layer
When the contact angle of the water on the surface of relative toner image receiving layer before heating and the difference after heating and cooling when big, this difference can cause release agent to be transferred on the surface of toner image receiving layer.
Particularly, with θ
0[°] and θ
1[°] receive before the thin slice contact angle of the water on the surface of toner image receiving layer relatively and image is received thin slice and be heated to 120 ℃ of contact angles after then it being cooled to 25 ℃ as adding thermal pattern respectively, satisfy following formula:
θ
1-θ
0≥5[°]
The difference of this contact angle approximate or greater than 8[°].
The contact angle of water can pass through sessile drop method, and the contact angle measurement that for example uses Kyowa interface science company limited to produce is measured.
The solid state properties of<visual receiving layer 〉
The toner image receiving layer preferably has high whiteness.Particularly, measure according to the assay method that satisfies JIS 8123, this toner image receiving layer preferably has and is higher than 85% whiteness.This toner image receiving layer also preferably has the spectral reflectivity greater than 85% in the wavelength coverage of 440-460nm, and the difference of high spectrum reflection rate and minimum spectral reflectivity more preferably has the spectral reflectivity greater than 85% less than 5% in the wavelength coverage of 400-700nm.
When adopting CIE 1976L
*a
*b
*When the color space was represented whiteness, the toner image receiving layer preferably had greater than 80, more preferably greater than 85, most preferably greater than 90 L
*Value.
Preferred white is neutral as far as possible, in other words, and with CIE 1976L
*a
*b
*The value ((a that the color space is represented
*)
2+ (b
*)
2) preferably less than 50, be more preferably less than 18, most preferably less than 5.
The toner image receiving layer preferably has higher glossiness.Particularly, 45 ° glossiness is preferably greater than 60, more preferably greater than 75, most preferably greater than 90.Yet in the scope with black state of the highest toner density, 45 ° high gloss is preferably less than 110 in the white states that does not have toner.If 45 ° of glossiness surpass 90, the toner image receiving layer forms the gloss image with metalloid gloss, and this is unfavorable.Glossiness can be measured by the assay method that satisfies JIS Z8741.
The toner image receiving layer preferably has higher smoothness.Particularly, preferably less than 3 μ m, be more preferably less than 1 μ m, with the smoothness of arithmetic average roughness (Ra) expression most preferably less than 0.5 μ m.Arithmetic average roughness (Ra) can be measured by the assay method that satisfies JIS B0601, B0651 and B0652.
The toner image receiving layer preferably has in following solid state properties (1)-(8) at least a:
(1) glass temperature of toner image receiving layer (Tg) preferably is higher than 30 ℃, but its glass temperature that exceeds toner is no more than 20 ℃;
(2) the toner image receiving layer has preferred 60-120 ℃, more preferably 80-170 ℃ 1/2 melt temperature (T1/2).In this case, 1/2 melt temperature (T1/2) was meant after 50 ℃ of 300 seconds of following preheating, when its temperature straight line being risen toner image receiving layer heating in the cylinder, begin to flow out the toner image receiving layer to half temperature of the stroke of piston that finishes to flow out in specific environment and specific extruding under the load from cylinder;
(3) the toner image receiving layer has and preferably exceeds the toner runoff and begin temperature and be no more than 50 ℃ runoff and begin temperature (Tfb);
(4) the toner image receiving layer has toner layer viscosity and reaches 1 * 10
5Temperature during CP is higher than 40 ℃ of temperature that still are lower than toner;
(5) the toner image receiving layer has 1 * 10 under fixed temperature
2-1 * 10
5The storage elastic modulus (G ') of Pa, and under fixed temperature, have 1 * 10
2-1 * 10
5The loss elastic modulus of Pa (G ");
(6) (G "/G ') is 0.01-10 to the angle of loss tangent of toner image receiving layer under fixed temperature, and (G ") represents with the ratio that fixed temperature is preserved elastic modulus (G ') down this angle of loss tangent with loss elastic modulus under the fixed temperature;
(7) the storage elastic modulus (G ') of toner image receiving layer under fixed temperature is that (G ' t)-50Pa is to preserving elastic modulus (in the scope of G ' t)+2500Pa for the storage elastic modulus of toner under fixed temperature.
(8) pitch angle of the relative toner image receiving layer of fusion toner is more preferably less than 4 ° preferably less than 50 °.
Preferably satisfy United States Patent (USP) 2,788,358 and Japanese unexamined patent publication No. publication number 7-248637,8-305067 and 10-239889 in the toner image receiving layer of disclosed solid state properties.
Above-mentioned solid state properties (1) can use the sensing equipment of differential scanning calorimeter well known in the art (DSC) to measure.Aforementioned solid state properties (2) and (3) can use the Flow Tester CFT-500 of for example Shimazu company production or the sensing equipment of CFT-500D to measure.Above-mentioned solid state properties (5)-(7) can use the rotation rheology instrumentation of the Dynamic AnalyzerRADII that Scientific company limited for example produces fixed.And above-mentioned solid state properties (8) can use the sensing equipment of for example Kyowa surface chemistry company limited production to measure by for example method described in the Japanese unexamined patent publication No. publication number 8-334916.
The toner image receiving layer has preferred 1 * 10 under the condition of the relative humidity of 25 ℃ temperature and 65%
6-1 * 10
15Ω/cm
2Surface resistivity.If surpass lower limit resistivity 1 * 10
6Ω/cm
2, this shows the quantity not sufficient of the toner of transferring to the toner image receiving layer, toner image density is tending towards diminishing so.On the other hand, if surpass upper limit resistivity 1 * 10
15Ω/cm
2, the electric charge of Chan Shenging will be above the required electric charge that shifts toner so.These excessive charges that produce make the transfer deficiency of toner, cause toner image density low, during the sclerosis electrophotographic image receives thin slice because of electric charge dust appears, wrong feeds electrons photographic image receives thin slice, repeats to present two or more thin slices, and printing of generation load and part toner do not take place shift.Toner image receiving layer in relative carrier one side preferably has 5 * 10
8-3.2 * 10
10Ω/cm
2, more preferably 1 * 10
9-1 * 10
10Ω/cm
2Surface resistivity.This surface resistivity can be used the sensing equipment mensuration of the R8340 of for example Advantest company limited production according to JIS K 6911.Particularly, in certain environmental conditions, promptly leave standstill sample image receiving layer more than 8 hours under 20 ℃ and 65% humidity after, apply 100V voltage on this same terms one minute next minute ground to it and measure this resistivity.
<other layer 〉
As foregoing, electrophotographic image receiving layer 1 can have other layer.The example of these layers comprises that sealer, backing layer, contact improve layer, middle layer, internal coating, cushion, antistatic control or antistatic layer, reflection horizon, color key-course, storage-stable raising layer, anti-bonding coat, anti-roll boundary layer and smooth layer.These layers can provide separately or can two or more mixing provide.
Sealer
Receive the ability of passing of thin slice 1 for surface, raising storage-stable, easy operating and the electrophotographic image of protecting electrophotographic image to receive thin slice 1; and make electrophotographic image reception thin slice 1 have writability and anti-skew patience, on the surface of toner image receiving layer 2, form sealer.Sealer can form two-layer or multilayer.Although various ger-bonds or thermosetting resin adhesive can be used for this sealer, preferably use ger-bond or the thermosetting resin adhesive identical with being used for the toner image receiving layer.The thermodynamics of the bonding agent of sealer and static characteristic be identical with the toner image receiving layer always not, and can optimization to satisfy this sealer.
Sealer can be mixed with adjuvant, the deluster of toner image receiving layer and the above-mentioned release agent of can be used for for example known in this field.Consider fixed performance, the top layer (sealer during formation) of photoelectric image reception thin slice 1 is preferably higher with the compatibility of toner.Particularly, sealer preferably has 0-40 ° contact angle ideally with the fusion toner.
Backing layer
Backing layer preferably forms on the photoelectric image relative with toner image receiving layer 2 receives the surface of carrier 3 of thin slice 1, so that provide reverse side to print adaptability and improve the reverse side print quality, crimping balance and electrophotographic image receive the ability of passing of thin slice 1.Although backing layer always is not subjected to the restriction of color, preferred it be white, and to receive thin slice 1 at photoelectric image be that preferred toner image receiving layer 2 also is a white under the two-sided situation.Backing layer preferably has whiteness and the spectral reflectivity greater than 85%, is similar to toner image receiving layer 2.In order to improve duplex printing adaptability, backing layer can be made up of single or multiple lift, and can be structurally identical with toner image receiving layer 2.And backing layer can be mixed with adjuvant, for example deluster and antistatic controlling agent.Form oil is being used for fixing under the situation of roller, backing layer is preferably the oil suction type.
Contact improves layer
Electrophotographic image receives thin slice 1 and preferably has a contact raising layer, so that improve the contact between toner image receiving layer 2 and the carrier 3.Contact improves layer can be mixed with various adjuvants, particularly comprises aforesaid crosslinking chemical.And electrophotographic image receives thin slice 1 and preferably has a cushion, to improve the toner acceptance between contact raising layer and the toner image receiving layer 2.
The middle layer
Electrophotographic image receives that thin slice 1 can improve between the layer at carrier 3 and contact, contact improves between layer and the cushion, between cushion and the toner image receiving layer 2 or toner image receiving layer 2 and storage-stable improve between the layer middle layer be provided.Under the situation that electrophotographic image reception thin slice 1 is made up of carrier 3, toner image receiving layer 2 and middle layer, nature is placed on the middle layer between carrier 3 and the toner image receiving layer 2.
Electrophotographic image with these additive layer receives thin slice 1 and is not subjected to the thickness constraint and preferably has 50-350 μ m, the more preferably thickness of 100-280 μ m for this purpose.
[toner]
In printing or copy application, electrophotographic image receives thin slice 1 and receive toner on toner image receiving layer 2.Toner contains at least a adhesive resin and colorant, also contains release agent and other component material in addition if necessary.
The toner binder resin
The preferred embodiment of the binder resin that can obtain includes, but not limited to styrene such as styrene and to chlorostyrene; Vinyl esters such as vinyl naphthalene, vinyl chloride, bromine ethene, fluorothene, vinyl acetate, propionate, vinyl benzoate and vinyl butyrate; Ethene alphatic carboxylic acid ester such as methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, dodecylacrylate, acrylic acid n-octyl, acrylic acid 2-chloroethene ester, phenyl acrylate, acrylic acid methyl α-chloromethyl ester, methyl methacrylate, Jia Jibingxisuanyizhi and butyl methacrylate; Vinyl nitrile such as vinyl cyanide, methacrylonitrile and acrylamide; Vinethene such as vinyl methyl ether; EVE and vinyl isobutyl ether; N-vinyl compound such as N-vinyl pyrrole, N-vinylcarbazole, N-vinyl indoles and N-vinyl pyrrolidone; Vinyl monomer such as vinyl carboxylate, for example homopolymer of methacrylic acid, acrylic acid or cinnamic acid or multipolymer; Polyester; They can use separately or can mix use with wax.The preferred use resin identical with the resinous type that is used for toner image receiving layer 2.
The toner colorant
The colorant that is used for conventional toner can use under the situation without any restriction.The preferred embodiment of the colorant that can obtain comprises, but be not limited to pigment such as carbon black, chrome yellow, Hansa yellow, benzidine yellow, the slen Huang, quinoline yellow, permanent orange GTR, the pyrazolone orange, the Vulcan orange, Watchung is red, permanent red, bright carmine 3B, brilliant carmine 6B, the Deipon oil red, pyrazolone is red, redole is red, rhodamine B lake, C lake red CAN'T, rose-red, aniline blue, ultramarine blue, the Carco oil blue, methylene blue chloride, phthalocyanine blue, phthalocyanine green and peacock green oxalates and dyestuff such as acridine dye, xanthene dye, azo dyes, dyes, the ninn dyestuff, anthraquinone dye, the sulfo-bipseudoindoxyl dye, two piperazine dyestuffs, thiazine dye, the azo methine dyes, bipseudoindoxyl dye, phthalocyanine dye, aniline black byestuffs, the polymethine dyestuff, triphenhlmethane dye, diphenylmethane dye and thiazole dye.These pigment or dyestuff can use separately or mix use with two or more.
The colorant content of toner is 2-8 weight % preferably.When this content is lower than down in limited time, can destroy the colouring power of colorant, and prescribe a time limit when this content is higher than, can make toner lose transparency.
Release agent
Although conventional known wax in principle can be as the release agent of toner, the preferred embodiment of release agent comprises, but be not limited to, have low-molecular-weight relatively highly crystalline Tissuemat E, Fischer-Tropsch wax, amide waxe and nitrogenous polar waxes such as urethane compound.Tissuemat E preferably has less than 1000, more preferably has the molecular weight of 300-1000.
Though it is little to have the compound molecular weight of urethane bond, the cohesiveness of its polar group makes it can keep solid-state, and has the high melt temperature with regard to small-molecular weight, therefore preferably uses it.The preferred feedstock of this compound comprises, but be not limited to the combination of the combination of the combination of the combination of diisocyanate cpd and monohydroxy alcohol, an isocyanate compound and monohydroxy alcohol, dibasic alcohol and an isocyanate compound, triol and an isocyanate compound and the combination of triisocyanate compound and monohydroxy alcohol.In order to prevent that this compound has higher molecular weight, importantly has the suitable functional group of quantity preferably with multifunctional and monofunctional compound combination, and for this compound.
The preferred embodiment of monoisocyanates includes, but not limited to derivant, naphthyl isocyanate, hexyl isocyanate, isocyanic acid benzene methyl, butyl isocyanate and the aryl isocyanate of isocyanic acid dodecyl ester, phenyl isocyanate, phenyl isocyanate.The preferred embodiment of diisocyanate comprises, but be not limited to, toluene diisocyanate, 4,4 ' methyl diphenylene diisocyanate, toluene diisocyanate, 1,3-phenylene vulcabond, hexamethylene diisocyanate, 4-methyl-metaphenylene diisocyanate and isophorone diisocyanate.
The preferred embodiment of monohydroxy alcohol includes, but not limited to methyl alcohol, ethanol, propyl alcohol, butanols, amylalcohol, hexanol and enanthol.
The preferred embodiment of dibasic alcohol includes, but not limited to various dibasic alcohol such as ethylene glycol, diethylene glycol, triethylene glycol, three methylene glycols etc.
The preferred embodiment of triol includes, but not limited to trimethylolpropane, triethylol propane, trimethylolethane etc.
Each compound can be joined in the toner with resin and/or colorant such as conventional release agent, so that the crushed toner of kneading is provided.When using these compounds by emulsification-polymerization-condense-when fusion method prepares toner, this compound is scattered in the water with polyelectrolyte such as ionic surface active agent, acidic polymer and alkaline polymer, be heated above the temperature of its melt temperature, and use homogenizer or pressure discharging dispersing apparatus that it is trimmed to particulate less than 1 μ m.The dispersion liquid of release agent particulate and the dispersion liquid of resin particle and/or the dispersion liquid one of colorant particles can be used from this colorant.
Other component of toner
Toner can be mixed with other component such as adjuvant, antistatic controlling agent, inorganic particles etc.
The example of adjuvant is a magnetic material, includes, but not limited to ferrite, magnetic iron ore, reduced iron, cobalt, nickel, manganese and combination thereof.
The preferred embodiment of antistatic controlling agent includes, but not limited to the complex compound and the triphenyl methane pigment of dyestuff such as quarternary ammonium salt compound, nigrosine compound, aluminium, iron or chromium.Consider condense and fusion during can influence toner stability to the control of ionic strength, simultaneously in order to reduce contaminated wastewater, the preferred material that is insoluble in water that uses.
What can be used as the inorganic particles use is all the conventional toner adjuvant that can adhere to toner-particle, for example silicon dioxide, titania, lime carbonate, magnesium carbonate, tricalcium phosphates etc.These inorganic particles disperse with ionic surface active agent, acidic polymer or alkaline polymer.
For emulsion polymerization, seeding polymerization, dispersed color, dispersion resin particle, dispersion release agent, and it is condensed and stablize, can use surfactant.The surfactant that can use simultaneously is anionic surfactant such as sulfuric acid surfactant, sulfosalt surfactant, phosphate ester surfactants, soap etc.; Cationic surfactant such as amine salt surfactant, quaternary surfactant etc.; With non-ionic surfactant such as polyalcohols etc.
Toner can add with the adjuvant that can adhere to toner-particle.The preferred embodiment of adjuvant includes, but not limited to following inorganic particle or powder: SiO
2, TiO
2, CuO, ZnO, SnO
2, Fe
2O
3, MgO, BaO, CaO, K
2O, NaO
2, ZrO
2, CaOSiO
2, K
2O (TiO
2)
n, Al
2O
32SiO
2, CaCO
3, MgCO
3, BaSO
4, MgSO
4Deng, and following organic granular or powder: the derivant of fatty acid, fatty acid, their metal acid, fluorocarbon resin, polyvinyl resin, acryl resin etc.These particles or powder preferably have 0.01-5 μ m, the more preferably mean grain size of 0.1-2 μ m.
Although can use the produced in several ways toner, the preferred method that may further comprise the steps (i)-(iii) of using:
(i) by in the dispersion liquid of resin particle, forming the resin particle that condenses, prepare the step of the dispersion liquid of the resin particle that condenses;
The step of (ii) mixing the particle that condenses that forms bonding particulate with the dispersion liquid of particulate by the dispersion liquid of the resin particle that will condense; With
(iii) the particle heating and melting that condenses of bonding particulate is formed the step of toner-particle.
The solid state properties of toner
Toner preferably has the volume average particle size of 0.5-10 μ m.If mean grain size is lower than this lower limit, can the operating performance (supply property, cleaning efficiency, flowability etc.) of toner be had a negative impact, and cause toner-particle underproduce.On the other hand, if mean grain size surpasses its upper limit, toner is understood owing to graininess and mobility, and the quality and the resolution of image is had negative effect.
Electrophotographic image is received thin slice, the volume average particle size profile exponent (GSDv) of preferred used toner is less than 1.3, and volume average particle size profile exponent (GSDv) is equal to or greater than 0.9 with the ratio (GSDv/GSDn) of average number particle diameter distribution index (GSDn), satisfies the requirement of volume average particle size simultaneously.In addition, the preferred electron photographic image receives the used toner of thin slice in the requirement of satisfying volume average particle size, also has the profile factor mean value of 1.00-1.50.The computing formula of the described profile factor is as follows:
The profile factor=(π * L
2)/(4 * S)
Wherein L is the maximum length of toner-particle, and S is the projected area of toner-particle.
When toner satisfies above-mentioned requirements, toner has positive effect to improving image quality, particularly aspect the resolution of graininess and image, and preventing the part toner does not have to shift and/or fuzzy toner image, generally can not have a negative impact simultaneously, even its mean grain size is always not little to its handling property.
In order to improve image quality, and prevent to be offset in the toner image fixation procedure, this storage elastic modulus (G ') when measuring with the angular frequency of 10rad/sec under 150 ℃ temperature of preferred toner is 10-200Pa.
[image formation method]
A kind of method of using the electronic photographing device that is equipped with fixed band to receive formation image on the thin slice 1 at electrophotographic image according to embodiment of the present invention that will be referred to is below described.In the following description, used " the fixedly banding pattern electronic photographing device " in this paper back is meant to have the electronic photographing device that at least one is used for fusion and heating of compacting toner and pressurized segment, one receives the fixed band of thin slice 1 with the contacted conveying electronic photographic image of toner image receiving layer; And a toner image fixed station, at this electrophotographic image that is heated is received thin slice 1 cooling and keep itself and the contacting of fixed band simultaneously.
In image formation method according to first embodiment, be loaded with the electrophotographic image that shifts the toner image that comes on it and receive thin slice 1 through fixed band and roller heating and compacting, cooling is taken off from fixed band afterwards then.In image formation method according to second embodiment, the electrophotographic image that is loaded with the toner image that shifts on it receives thin slice 1 through heating and/or backer roll heating, with fixing toner image, then through fixed band and roller heating with pressurize, cooling is taken off from fixed band afterwards then.The known toner image transfer system that many types are arranged.These two kinds of image formation methods can comprise the toner image transfer system that well known to a person skilled in the art any kind.The preferred embodiment of toner image transfer method includes, but not limited to direct toner image transfer method, wherein the toner image that develops on the developer roll is directly transferred to electrophotographic image and is received thin slice; And middle band transfer method, be with in the middle of wherein at first toner image being transferred to, and then transfer on the electrophotographic image reception thin slice.Consider environmental stability and image quality, electrophotographic image is with transfer system in the middle of receiving thin slice 1 preferred the use.Disclose to be equipped with described in various fixedly banding pattern electronic photographing devices such as the Japanese unexamined patent publication No. publication number 11-352819 to have or not and finished the electronic photographing device that second toner image shifts and toner image is fixing described in the electronic photographing device of oily fixed band and for example Japanese unexamined patent publication No. publication number 5-341666 and the 11-352819 simultaneously.
For fixing banding pattern electronic photographing device, adhere to the toner that electrophotographic image receives on the toner image receiving layer of thin slice 1 and obtain meticulous fixingly because of fusion, not diffusion, and when keeping in touch with fixed band is cooled off and is solidified.As a result, toner is received and is imbedded in fully in the toner image receiving layer 2.Therefore, electrophotographic image receives thin slice 1 provides and has gloss and smooth and do not have a toner image of projection.
Fixedly under the situation of banding pattern electronic photographing device, importantly electrophotographic image reception thin slice 1 makes moderate progress aspect skew at the nothing oil that uses image formation method to be applicable to that electrophotographic image receives thin slice 1.And, using other fixedly under the situation of banding pattern electronic photographing device, except the raising of offset characteristic, also improve the quality that electrophotographic image receives the full-colour image that thin slice 1 provided, and prevented the appearance of ftractureing.As known, according to type, color electronography equipment comprises that image receives thin slice carrying part, latent image and forms part and be positioned at equipment center and receive thin slice carrying part and latent image at image and form middle tone toner image transfer part in the middle of the part.
Known have various image formation methods that improve image quality that are applicable to, for example adhesive transfer method or heat help transfer method to replace electrostatic transfer method or two roller transfer method, or are used in combination with it.These transfer methods are disclosed in for example Japanese unexamined patent publication No. publication number 63-113576 and 5-341666.Especially preferably use heat to help transfer method, wherein particularly under the situation of using the little toner of particle diameter, use intermediate transfer.And it is preferred after the toner image transition phase or in the second half section of toner image transition phase, for the centre band is equipped with a cooling device.This cooling device is cooled to the melt temperature of the adhesive resin that is lower than toner with the temperature of the toner that shifts or is lower than the high 10 ℃ temperature of glass temperature of specific viscosity mixture resin.This makes toner image transfer to electrophotographic image effectively and receives on the thin slice 1, and is easy to make electrophotographic image reception thin slice 1 to separate with intermediate transfer.
Image fixedly is the glossiness of the final image of control and the significant process of smoothness.Known roller fixation procedure and the fixing band fixation procedure of use band that has heating used and/or backer roll to fix.Consider image quality, promptly gloss and smooth image preferably are with fixation procedure.The preferred embodiment of band fixation procedure comprises, but be not limited to, use the process of disclosed no oily fixed band among the Japanese unexamined patent publication No. publication number 11-352819 for example and disclosed second image transfer and the fixing process of image of realizing simultaneously among Japanese unexamined patent publication No. publication number 5-341666 and the 11-352819 for example.
In order to prevent that toner from peeling off and/or being offset, fixed band can fluoridize on its surface and/silication.Preferred fixed band is attended by cooling device, fixed band is cooled off with the second half section in fixation procedure, separates with fixed band thereby easily electrophotographic image is received thin slice 1.This cooling device can be cooled to the toner that shifts the temperature of the melt temperature of the adhesive resin of the toner that is lower than toner image receiving layer 2 and/or polymkeric substance, perhaps is cooled to the high 10 ℃ temperature of glass temperature that is lower than specific viscosity mixture resin.On the other hand, when beginning fixedly, toner image receiving layer or its toner that electrophotographic image receives thin slice 1 must fully be heated to its melt temperature.According to these conditions, preferably chilling temperature is fixed in 30-70 ℃ the scope feasiblely, and when beginning fixedly, is set in 100-180 ℃ the scope.
A fixedly example of banding pattern electronic photographing device 2 is described with reference to the accompanying drawings in this paper back.After the toner image transition phase is transferred to toner 12 electrophotographic image reception thin slice 1, the electrophotographic image that is stained with toner 12 is received thin slice 1 be transported to fixed position A, in other words, between warm-up mill 14 and backer roll 15.During passing roller 14 and 15, toner image receiving layer 2 or toner 12 that electrophotographic image receives thin slice 1 fully are heated under fixation pressure to its melt temperature (fixed temperature).In this case, the electrophotographic image that the roll gap of fixed temperature representative between heating and backer roll 14 and 15 measured receives the surface temperature of thin slice 1, and preferably at 80-190 ℃, more preferably in 100-170 ℃ the scope.The pressure that the roll gap of fixation pressure representative between heating and backer roll 14 and 15 measured, and preferably at 1-10kg/cm
2, more preferably 2-7kg/cm
2Scope in.Receive thin slice 1 through the electrophotographic image of heating and pressurization and transport as the endless belt, by cooling device 16 through fixed band 13.Before arriving cooling device 16, the release agent that is present in dispersedly in the toner image receiving layer 2 heats and fusion through abundant, and the result separates the formation film on toner image receiving layer 2.Receive thin slice 1 by in the cooling device 16 at electrophotographic image, electrophotographic image receives the temperature that thin slice 1 is cooled to the melt temperature of the adhesive resin of the toner that is lower than toner image receiving layer 2 and/or polymkeric substance, perhaps be cooled to the high 10 ℃ temperature of glass temperature that is lower than specific viscosity mixture resin, be cooled to 20-80 ℃ ideally, more preferably from about the temperature of 25 ℃ room temperature.Receiving thin slice 1 by the cool electronic photographic image, is release layer with the release agent film hardening that forms on the toner image receiving layer 2.
Electrophotographic image after the cooling receives thin slice 1 and further is transported to the demoulding position B that places jockey pulley 17.In demoulding position, jockey pulley 17 guiding fixed bands 13 separate so that itself and electrophotographic image are received thin slice 1.In this case, jockey pulley 17 preferably has enough little diameter and relies on himself rigidity to peel off from fixed band 13 so that electrophotographic image receives thin slice 1.The preferred annular fixed band of making by stock such as polyimide, electricity system nickel or aluminium that uses.
Fixed band 13 preferably is being coated with the film that is selected from following material more than at least a on its film: polysiloxane rubber, carbon fluororubber, polyorganosiloxane resin and fluorocarbon resin.More preferably, on fixed band 13, form the uniform carbon fluorine of thickness polysiloxane rubber film aptly, perhaps form the uniform polysiloxane rubber film of thickness, and on the polysiloxane rubber film, form carbon fluorine polysiloxane rubber film.
Preferably use the carbon fluorine polysiloxane rubber that in main chain, has perfluoroalkyl ether group and/or perfluoroalkyl.The preferred embodiment of carbon fluorine polysiloxane rubber is a kind of hardening composition that contains following component: fluorocarbon polymer (component A), it contains the carbon fluorosilicone as key component and have aliphatic unsaturated group, organopolysiloxane and/or carbon fluorosilicone (B component), it in a molecule, contain plural ≡ SiH group and ≡ SiH group content in molal weight be the amount of aliphatic unsaturated group in the carbon fluorine polysiloxane rubber composition 1-4 doubly, filler (component C) and effective dose catalyzer (component D).
Component A, promptly fluorocarbon polymer has following general formula (I) as the repetitive of key component and the carbon fluorosilicone of aliphatic unsaturated group.
General formula (I)
R wherein
10Be have a 1-8 carbon atom can replace the monovalence alkyl that maybe can not replace, preferably have the alkyl of 1-8 carbon atom or have the alkenyl of 2 or 3 carbon atoms, be more preferably methyl; A and e are value 0 or 1; B and d are the integers of 1-4, and c is the integer of 0-8, and x is the integer greater than 1, and 10-30 preferably.
Instantiation is the polymkeric substance with following formula (II):
Formula (II)
B component promptly has the organopolysiloxane of ≡ SiH group, is the organic hydrogen polysiloxanes that at least 2 hydrogen atoms that link to each other with silicon atom are arranged in a molecule.With regard to carbon fluorine polysiloxane rubber composition, as component A, i.e. fluorocarbon polymer when having aliphatic unsaturated group, can use organic hydrogen polysiloxanes as rigidizer.That is, in this case, in aliphatic unsaturated group by the carbon fluorosilicone and the organic hydrogen polysiloxanes with hydrogen atom that silicon atom links to each other between the addition reaction that causes form a hardening composition.The various organic hydrogen polysiloxanes that are used for the rubber composition of addition curable can be used as the organic hydrogen polysiloxanes of composition B.
Preferred group is should organic hydrogen polysiloxanes, so that an aliphatic unsaturated hydrocarbon base of carbon fluorosilicone among the component A is had at least one, and preferred 1-5 ≡ SiH group.
B component promptly has the preferred embodiment of the carbon fluorosilicone of ≡ SiH group, is the R that has the unit of general formula (I) or have general formula (I)
10For dialkyl group hydrogen siloxy and SiH group (as dialkyl group hydrogen siloxy or silicyl) as end group, and have the carbon fluorosilicone of following formula (III)
Formula (III)
The preferred embodiment of component C comprises, but be not limited to, the various fillers that are usually used in conventional rubber composition, filler such as gasoloid silicon dioxide, precipitable silicon dioxide, carbon dust, titania, aluminium oxide, silica flour, talcum, sericite and bentonitic clay and fiberfill such as asbestos, glass fibre and organic fiber promptly harden.
The preferred embodiment of the catalyzer of component D comprises; but be not limited to; complex compound, three (triphenyl phasphine) the chlorine rhodium (Wilkinson catalyzer) of the complex compound of chloroplatinic acid, chloroplatinic acid and the alkene of known various catalyzer that are used for addition reaction such as chloroplatinic acid, pure modification, the platinum black that carries alumina or palladium, the platinum black that carries silicon dioxide or palladium, the platinum black that carries carbon or palladium, rhodium and alkene, pentanedione acid rhodium (III), they are VIII family element and compounds thereof in the periodic table.Preferred these complex compounds use with the form of alcoholic solution, ethereal solution, hydrocarbon solution.
In the scope of not damaging the object of the invention, the carbon fluorine polysiloxane rubber as component D can be added with various compounding ingredients.The example of compounding ingredient includes, but not limited to spreading agent such as diphenyl silanodiol, has the oligomeric dimethyl polysiloxane of dimethyl polysiloxane at the end of strand; Thermotolerance improving agent such as iron protoxide, iron oxide, cerium oxide, iron octoate; With colorant such as pigment.
Fixed band is by one deck carbon fluorine polysiloxane rubber composition is coated on heat stable resin or the metal tape, and heating makes its curing.If necessary, fixed band can be coated with by conventional rubbing method such as spin coating, dip-coating or cutter, uses the coating fluid that makes with solvent such as hexafluoro m-xylene or benzotrifluoride dilution carbon fluorine polysiloxane rubber composition to be coated with.Be not subjected to the restriction of temperature and time although be heating and curing, according to preferred heating 5 second-5 hour under 100-500 ℃ temperature of type belt (type belt) material and band job operation.Although the carbon fluorine polysiloxane rubber composition layer of fixed band always is not subjected to the restriction of thickness, preferred this layer thickness is 20-500 μ m, more preferably 40-200 μ m.
Receive the electrophotographic method that forms image on the thin slice 1 at electrophotographic image and be not limited to the method for being undertaken,, and comprise the method that forms full-colour image by conventional color electronography equipment as long as use fixed band by electronic photographing device shown in Figure 2.
Therefore image formation method of the present invention has prevented to separate between electrophotographic image reception thin slice 1 and the toner, has perhaps prevented to be offset between electrophotographic image reception thin slice 1 and the toner component, thereby has realized that the stable of thin slice transports.Receive at electrophotographic image like this and form gloss image on the thin slice 1 with photographic quality.