TECHNICAL FIELD The present invention relates to a method of forming fixed images used for plain paper copying machines, laser printers, plain paper facsimiles, etc. More particularly, it relates to a method of forming images in which low temperature fixing is carried out using a thermally dissociating encapsulated toner.

BACKGROUND ART

Conventionally, when images are formed with copying machines, laser beam printers, etc., the Carlson Method has been generally used (U.S. Patent 2,221,776, 2,297,691 and 2,357,809, "Electrophotography," p22-pϋ1 , R.M. Shaffert, 1965, The Focal Press).

Figure 2 shows a schematic view of an apparatus for a conventional method of forming fixed images. In the conventional method, after the electrostatic latent image formed on a photoconductor by optical means is developed in a developing process, it is transferred to a recording medium such as recording paper in a transfer process and then fixed into the final image generally with heat and pressure in a fixing process. As the photoconductor is repeatedly used, a cleaning device is provided for cleaning the residual toner after the transfer process with its rotation.

In the conventional method of forming fixed images, however, through the processes from the formation of the electrostatic latent image up to its fixing onto the recording medium, the temperature of the heating element of the fixing device has to remain at a very high level (usually around 200°C ) and further a relatively high nip pressure is required (usually between 2.0 and 6.0 kg/cm). On the other hand, since both the photoconductor and the developing device have to be maintained at around room temperature, a considerable distance has to be maintained between the fixing device and the developing device, which necessitates to make the machine larger. In addition, it is necessary to force the removal of the generated heat from the system, but the noise produced by the forced radiation device is not negligible.

Further, in the conventional method of forming fixed images, since the fixing section works independently and at such a high temperature of around 200°C , as mentioned above, expensive heat-resistant materials such as heat-resistant resins, heat-resistant rubbers, etc. have to be provided around the fixing device.

When the fixing is carried out at a high temperature, it is subject to problems such as curling and jamming of the paper, etc. In addition, it is pointed out that a fixing failure may take place due to the heat absorbed by the paper, depending upon its thickness. Further, if the fixing requires a high temperature, it takes more time to reach the set temperature so that a quick printing becomes impossible.

In such a case, therefore, this method is unsuitable for devices such as a facsimile which requires quick printings.

As for solving these problems, a device for carrying out low temperature fixing using a cold pressing method (Japanese Patent Laid-Open No. 159174/1984) is known. In this reference, however, although the fixing temperature is low, the nip pressure has to be elevated normally to not less than 4 kg/cm in this method, making the machine heavier. Moreover, it poses problems in the gloss of the images, deformation of the paper copy sheets and an insufficient fixing strength. As for a fixing device for fixing images at such a low nip pressure of less than 4 kg/cm, a heat roller method is known, for example, but it has been pointed out that the fixing temperature needs to be maintained at not less than 120°C-

Under the circumstances, the development of a fixing device that can fix images at a low temperature and at a low nip pressure is highly desired, but it has not yet been developed. Further, as regards toners to be indispensably used for the image formation, since they have been confined to those made from a thermoplastic resin dispersed with additives such as coloring agents, charge control agents, releasing agents, etc., and pulverized, there have been limitations on the molecular weight, the softening point of the thermoplastic resin for use in the toner from the aspect of storage stability, thereby posing limitations on the further pursuit of low temperature fixing.

From these standpoints, the development of a novel

method of forming fixed images as well as a matching toner thereto is in demand.

DISCLOSURE OF INVENTION An object of the present invention is to provide a novel method of forming fixed images, wherein an extremely low fixing temperature as well as a low nip pressure is utilized so that the radiator can be made much smaller and the noise substantially reduced, thus providing advantageous results such as the reduction of curling and jamming of the paper sheets and quick printing.

Therefore, in view of solving the above-mentioned problems, the present inventors have investigated a toner shell material which is fragile to heat at a low temperature. As a result, they have found that a thermally dissociating encapsulated toner produced by interfacial polymerization melts at a temperature of not more than 120°C , and they have further investigated the image formation method using this encapsulated toner and have thus developed the present invention.

More particularly, the method of forming fixed images of the present invention comprises charging a photoconductor; exposing the photoconductor to light; developing an electrostatic latent image whereby a toner is applied to the electrostatic latent image formed on the photoconductor to form a visible image; transferring the formed visible image to the recording medium; and fixing the transferred visible image onto the recording medium, wherein the fixing process

comprises preheating the toner transferred onto the recording medium using an endless heating film and then pressure-fixing the toner.

In addition, it is a method of forming fixed images, wherein a toner is a thermally dissociating encapsulated toner, and wherein the preheating temperature of the toner transferred onto the recording medium is 40°C to 120°C , and wherein the nip pressure in the fixing process is 0.5 to 4 kg/cm. According to the present invention, in the fixing process, since the pressure-fixing is carried out after preheating the toner, fixing can take place at a low temperature. Therefore, the fixing device can be simplified, making it possible to miniaturize the fixing device and lower the cost thereof. Further, since the fixing is carried out at a fixing temperature of not more than 120 ^β C , it is not required to use heat-resistant members for the fixing device and the periphery thereof, and inexpensive materials can be used therefor. In addition, the durability of the members used becomes long, which makes it possible to produce a low-cost printing device. Moreover, since the fixing temperature is very low, problems such as the curling and the jamming of the paper sheets are less likely to occur, and thus conserving in its maintenance. Further, since the toner capable of fixing at a low temperature is used, the temperature of the heating elements arranged in the fixing device can be set at a lower temperature than the case where the ordinary toner is used.

- Therefore, a forced radiation device such as an electric fan, etc. can be made smaller or is not required, thereby making it possible to reduce the noise problems. Further, the low fixing temperature reduces the time before the set temperature is reached, making quick printing possible. The low nip pressure reduces low line resolution and blur of the print image, thereby providing a high quality image and further making the durability of the fixing roller longer.

BRIEF DESCRIPTION OF DRAWINGS

The present invention will become more fully understood from the detailed description given hereinbelow and the accompanying drawings which are given by way of illustration only, and thus, are not limitative of the present invention, and wherein:

Figure 1 is a schematic view of an apparatus used in the method of forming fixed images as defined by the present invention;

Figure 2 is a schematic view of an apparatus used for conventional methods of forming fixed images;

Figure 3 is a schematic view showing the charging process in the method as defined by the present invention;

Figure 4 is a schematic view showing the exposing process in the method as defined by the present invention; Figure 5 is a schematic view showing the developing process in the method as defined by the present invention;

Figure 6 is a schematic view showing the transfer process in the method as defined by the present invention;

Figure 7 is a schematic view of the fixing process in the method as defined by the present invention;

Figure 8 is a schematic view showing a cross section of the endless heating film used in the fixing process in the method as defined by the present invention;

Figure 9 is a schematic view of the fixing process in the method as defined by the present invention; and

Figure 10 is a schematic view of the fixing process in the method as defined by the present invention. The reference numerals in Figures 1 through 10 denote the following elements: Element 1 is a photoconductor, element 1a a photoconductive layer, element 1b a conductive supporter, element 2 an exposure device, element 3 a developer device, element 3a a rotating sleeve, element 5b a transfer device, element 6 a recording medium (a recording paper), element 7 a charger, element 8 a cleaner device, element 8a a toner collecting, box, element 8b a cleaning web, element 9 a charge eraser, element 10 a toner, element 11 an endless heating film, element 11a a conductive layer, element 11b a heating layer, element 11c a conductive layer, element lid an insulating releasing layer, element He a terminal, element 11f a terminal, element 12a a fixing roller ( ^•* > pressure roller), element 12b a fixing roller (a pressure roller), element 14 a heat roller, element 15 a conveyor belt, and element 16 a holding roller.

BEST MODE FOR CARRYING OUT THE INVENTION

The toner used in the present invention is a thermally

dissociating encapsulated toner. The encapsulated toner according to the present invention comprises a heat-fusible core containing at least a coloring agent and a shell formed thereon so as to cover the surface of the core material. In the present invention, the thermally dissociating encapsulated toner means a toner which comprises a shell whose structure is fragile to heat, and a core material which can be fixed at a low temperature by pressure. More particularly, the shell structure changes with heat, and at the point where pressure is applied, the core material is discharged to effect the fixing of the toner. Depending on the raw materials and production method, a large variety of encapsulated toners are conceivable, and as long as they are within the range of the required thermal properties, there are no limitations on what production process or materials are used. The toner in the present invention is a thermally dissociating encapsulated toner, and any toner whose fixing temperature is maintained in the range of 40 to 120°C to the recording medium such as a recording paper can be properly chosen.

As to the method for producing the encapsulated toners, the following can be mentioned.

(1) Spray-drying method

After the core material is dispersed in a non-aqueous solution of polymer or polymer-emulsion, the dispersed liquid is spray-dried.

(2) Phase separation method (coacervation method)

In a solution of ionic polymer colloids and the core

material, . ase separation is conducted around the core material. In other words, a simple emulsion is first prepared, which in turn is converted to a complex emulsion, in which the core materials are micro-encapsulated. (3) Interfacial polymerization method

A core material solution or dispersion is dispersed in a water in oil or oil in water type emulsion system, while at the same time shell material monomers (A) are collected around the surfaces, where in the next method, monomers (A) and monomers (B) react.

(4) Other methods include an in-situ polymerization method, a submerged cure coating method, an air suspension coating method, an electrostatic coalescing method, a vacuum vapor deposition coating method, etc. The particularly preferred toners include those produced by the interfacial polymerization method and the spray-drying method. While the spray-drying method has the merits of an easy function separation for the core material and shell material and a large choice of shell materials, the interfacial polymerization method not only has the merit of an easy function separation for the core material and shell material but also is capable of producing a uniform toner in an aqueous state. Moreover, substances of low softening points can be used for the core material in the interfacial polymerization method, making it particularly suitable from the aspect of fixing ability. Accordingly, in the present invention, the thermally dissociating encapsulated toner produced by the interfacial

polymerization method among others is particularly preferred.

For shell materials, styrene resins (Japanese Patent Laid-Open No.205162/1983) , polyamide resins (Japanese Patent Laid-Open No.66948/1983) , epoxy resins (Japanese Patent Laid-Open No.148066/1984) , polyurethane resins (Japanese Patent Laid-Open No.179860/1982), polyurea resins (Japanese Patent Laid-Open No.150262/1987) and many others have been proposed. And as substances fixible under heat and pressure contained in the core material, thermoplastic resins such as polyester resins, polyamide resins, polyester-polyamide resins, and vinyl resins having glass transition points (Tg) between 10°C and 50°C can be used.

As compared to the thermal properties of the core material, the structure and the thermal properties of the shell material concern themselves remarkably with the fixing ability of the entire toner. Since a particular polyurethane resin among the above-mentioned resins for the shell materials is thermally dissociating, having excellent storage stability and fixing ability at a low temperature, it is an extremely favorable material for the method of forming fixed images of the present invention. As principal components of such a shell material, resins obtainable from the reaction between an isocyanate compound and/or isothiocyanate compound and compounds containing a phenolic hydroxy group and/or a thiol group are preferably used (EP0453857A).

The thermally dissociating encapsulated toner suitably

used in the present invention can be produced by any known methods such as interfacial polymerization, etc., and this encapsulated toner is composed of a heat-fusible core material containing at least a coloring agent and a shell formed thereon so as to cover the surface of the core material, wherein the main components of the shell are a resin prepared by reacting:

(A) an isocyanate and/or isothiocyanate compound comprising: (1) 0 to 30 mol ^" 5 of a monovalent isocyanate and/or isothiocyanate compounds, and

(2) 100 to 70 mol % of at least a divalent isocyanate and/or isothiocyanate compounds with (B) an active hydrogen compound comprising:

(3) 0 to 30 mol % of a compound having one active hydrogen atom reactive with the isocyanate and/or isothiocyanate groups and

(4) 100 to 70 mol % of a compound having at least two active hydrogen atoms reactive with the isocyanate and/or .isothiocyanate groups at a molar ratio of the component (A) to the component (B) of between 1:1 and 1:20, and wherein at least 30% of all of the linkages formed from the isocyanate or isothiocyanate groups are thermally dissociating linkages.

According to the present invention, the thermally dissociating linkage is preferably one formed ^' by the reaction between a phenolic hydroxyl and/or thiol group and

an isocyanate and/or isothiocyanate group..

Examples of the monovalent isocyanate compounds to be used as the the component (1) in the present invention include ethyl isocyanate, octyl isocyanate, 2-chloroethyl isocyanate, chlorosulfonyl isocyanate, cyclohexyl isocyanate, n-dodecyl isocyanate, butyl isocyanate, n-hexyl isocyanate, lauryl isocyanate, phenyl isocyanate, m-chlorophenyl isocyanate, 4-chlorophenyl isocyanate, p-cyanophenyl isocyanate, 3,4-dichlorophenyl isocyanate, o-tolyl isocyanate, m-tolyl isocyanate, p-tolyl isocyanate, p-toluenesulfonyl isocyanate, 1-naphthyl isocyanate, o-nitrophenyl isocyanate, m-nitrophenyl isocyanate, p-nitrophenyl isocyanate, p-bromophenyl isocyanate, o-methoxyphenyl isocyanate, m-methoxyphenyl isocyanate, p-methoxyphenyl isocyanate, ethyl isocyanatoacetate, butyl isocyanatoacetate and trichloroacetyl isocyanate.

Examples of the divalent or higher isocyanate compounds to be used as the component (2) in the present invention include aromatic isocyanate compounds such as 2,4-tolylene diisocyanate, 2,4-tolylene diisocyanate dimer, 2,6-tolylene diisocyanate, p-xylylene diisocyanate, -xylylene diisocyanate, 4,U' -diphenylmethane diisocyanate, 1,5- naphthylene diisocyanate, 3,3' -dimethyldiphenyl-4,4' - diisocyanate, 3,3'-dimethyldiphenylmethane-4,4'-diisocyanate, m-phenylene diisocyanate, triphenylmethane triisocyanate and polymethylenephenyl isocyanate; aliphatic isocyanate compounds such as hexamethylene diisocyanate,

trimethylhexamethylene diisocyanate, l.ysine diisocyanate and dimer acid diisocyanates; alicyclic isocyanate compounds such as isophorone diisocyanate, 4,4' -methylenebis- (cyclohexyl isocyanate), methylcyclohexane-2,4(or 2,6)- diisocyanate and 1 ,3-(isocyanatotnethyl)cyclohexane; and other isocyanate compounds such as an adduct of 1 mol of tri ethylolpropane with 3 mol of tolylene diisocyanate.

Examples of the isothiocyanate compounds include phenyl isothiocyanate, xylylene-1 ,4-diisothiocyanate and ethylidene diisothiocyanate.

Among these isocyanate and isothiocyanate compounds, compounds having an isocyanate group directly bonded to an aromatic ring are preferred, because they are effective in forming a urethane resin having a low thermal dissociation temperature.

According to the present invention, the monovalent isocyanate and/or isothiocyanate compound (1) also serves as a molecular weight modifier for the shell-forming resin and can be used in an amount of at most 30 mol % based on the isocyanate component and/or the isothiocyanate component. When the amount exceeds 30 mol % , the storage stability of the obtained encapsulated toner is undesirably poor.

Examples of compounds having one active hydrogen atom reactive with isocyanate and/or isothiocyanate groups to be used as component (3) in the present invention include aliphatic alcohols such as methyl alcohol, ethyl alcohol, propyl alcohol, isopropyl alcohol, butyl alcohol, isobutyl alcohol, tert-butyl alcohol, pentyl alcohol, hexyl

- -

alcohol, cyclohexyl alcohol, heptyl alcohol, octyl alcohol, nonyl alcohol, decyl alcohol, lauryl alcohol and stearyl alcohol; aromatic alcohols such as phenol, o-cresol, m-cresol, p-cresol, 4-butylphenol, 2-sec-butylphenol, 2-tert-butylphenol, 3-tert-butylphenol, 4-tert-butylphenol, nonylphenol, isononylphenol, 2-propenylphenol, 3-propenylphenol, 4-propenylphenol, 2-methoxyphenol, 3-methoxyphenol, 4-methoxyphenol, 3-acetylphenol, 3-carbomethoxyphenol, 2-chlorophenol, 3-chlorophenol, 4-chlorophenol, 2-bromophenol, 3-bromophenol, 4-bromophenol, benzyl alcohol, 1-naphthol, 2-naphthol and 2-acetyl-1- naphthol; and amides such as ε -caprolactam.

Particularly, a phenol derivative represented by the following formula (I) is preferably used:

OH

wherein Ri. R2. R3. Ru and R ₅ each independently represents a hydrogen atom, an alkyl group having 1 to 9 carbon atoms, an alkenyl, alkoxy, alkanoyl, carboalkoxy or aryl group or a halogen atom.

Examples of the dihydric or higher alcohols among the compounds having at least two active hydrogen atoms reactive with isocyanate and/or isothiocyanate groups to be used as the component (4) in the present invention include catechol, resorcinol, hydroquinone, 4-methylcatechol, 4-tert- butylcatechol, 4-acetylcatechol, 3-methoxycatechol,

4-phenylcatechol, 4-methylresorcinol, 4-ethylresorcinol , 4-tert-butylresorcinol, 4-hexylresorcinol, 4-chlororesorcinol, 4-benzylresorcinol, 4-acetylresorcinol, 4-carbomethoxyresorcinol, 2-methylresorcinol, 5-methylresorcinol, tert-butylhydroquinone, 2,5-di-tert- butylhydroquinone, 2,5-di-tert-amylhydroquinone, tetramethylhydroquinone, tetrachlorohydroquinone, methylcarboa inohydroquinone, methylureidohydroquinone, benzonorbornene-3,6-diol, bisphenol A, bisphenol S, 3,3'- dichlorobisphenol S, 2,2' -dihydroxybenzophenone,.

2,4-dihydroxybenzophenone, 4,4' -dihydroxybenzophenone, 2,2' -dihydroxydiphenyl, 4,4' -dihydroxydiphenyl, 2,2'- dihydroxydiphenylmethane, 3,4-bis(p-hydroxyphenyl)hexane, 1 ,4-bis(2-(p-hydroxyphenyl)propyl)benzene, bis(4- hydroxyphenyl)methylamine, 1 ,3-dihydroxynaphthalene, 1,4- dihydroxynaphthalene, 1 ,5-dihydroxynaphthalene, 2,6- dihydroxynaphthalene, 1 ,5-dihydroxyanthraquinone, 2-hydroxybenzyl alcohol, 4-hydroxybenzyl alcohol, 2-hydroxy- 3,5-di-tert-butylbenzyl alcohol, 4-hydroxy-3,5-di-tert- butylbenzyl alcohol, 4-hydroxyphenethyl alcohol,

2-hydroxyethyl 4-hydroxybenzoate, 2-hydroxyethyl 4- hydroxyphenylacetate, resorcinol mono-2-hydroxyethyl ether, hydroxyhydroquinone, gallic acid and ethyl 3,4,5- trihydroxybenzoate. Among these dihydric or higher alcohols, catechol derivatives represented by the following formula (II) and resorcinol derivatives represented by the following formula (III) are preferably used*

wherein Re. R7. Re and R9 each independently represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkenyl, alkoxy, alkanoyl, carboalkoxy or aryl group or a halogen atom.

OH

wherein Rio. Ri 1. Ri 2 and Ri 3 each independently represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkenyl, alkoxy, alkanoyl, carboalkoxy or aryl group or a halogen atom.

Further, examples of the compounds having at least one isocyanate- or isothiocyanate-reactive functional group other than the hydroxyl group and at least one phenolic hydroxyl group include o-hydroxybenzoic acid, m-hydroxybenzoic acid, p-hydroxybenzoic acid, 5-bromo-2- hydroxybenzoic acid, 3-chloro-4-hydroxybenzoic acid, 4-chloro-2-hydroxybenzoic acid, 5-chloro-2-hydroxybenzoic acid, 3,5-dichloro-4-hydroxybenzoic acid, 3-methyl-2- hydroxybenzoic acid, 5-methoxy-2-hydroxybenzoic acid, 3,5-di-tert-butyl-4-hydroxybenzoic acid, 4-amino-2- hydroxybenzoic acid, 5-amino-2-hydroxybenzoic acid, 2,5- dinitrosalicylic acid, sulfosalicylic acid, 4-hydroxy-3- methoxyphenylacetic acid, catechol-4-carboxylic acid, 2,4-

dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid, 2,6- dihydroxybenzoic acid, 3,4-dihydroxybenzoic acid, 3,5- dihydroxybenzoic acid, 3,4-dihydroxyphenylacetic acid, m-hydroxycinnamic acid, p-hydroxycinnamic acid, 2-amino-4- ethylphenol, 2-amino-5-methylphenol, 5-amino-2- methylphenol, 3-amino-2-naphthol, 8-amino-2-naphthol, 1-amino-2-naphthol-4-sulfonic acid, 2-amino-5-naphthol-4- sulfonic acid, 2-amino-4-nitrophenol , 4-amino-2-nitrophenol, 4-amino-2,6-dichlorophenol, o-aminophenol, m-aminophenol, p-aminophenol, 4-chloro-2-aminophenol, 1-amino-4- hydroxyanthraquinone, 5-chloro-2-hydroxyaniline, a -cyano-3- hydroxycinnamic acid, a -cyano-4-hydroxycinnamic acid, 1-hydroxynaphthoic acid, 2-hydroxynaphthoic acid, 3-hydroxynaphthoic acid and 4-hydroxyphthalic acid. Further, examples of the polythiol compounds having at least one thiol group in each molecule include ethanethiol, 1-propanethiol, 2-propanethiol, thiophenol, bis(2- mercaptoethyl)ether, 1 ,2-ethanedithiol, 1 ,4-butanedithiol , bis(2-mercaptoethyl) sulfide, ethylene glycol bis(2- mercaptoacetate), ethylene glycol bis(3-mercaptopropionate) , 2,2-dimethylpropanediol bis(2-mercaptoacetate) , 2,2- di ethylpropanediol bis(3-mercaptopropionate) , trimethylolpropane tris(2-mercaptoacetate) , trimethylolpropane tris(3-mercaptopropionate) , trimethylolethane tris(2-mercaptoacetate) , trimethylolethane tris(3-mercaptopropionate) , pentaerythritol tetrakis(2-mercaptoacetate) , pentaerythritol tetrakis(3-mercaptopropionate) ,

dipentaerythritol hexakis(2-mercaptoacetate) , dipentaerythritol hexakis(3-mercaptopropionate) , 1,2- dimercaptobenzene, 4-methyl-1 ,2-dimercaptobenzene, 3,6-dichloro-1 ,2-dimercaptobenzene, 3,4,5,6-tetrachloro-1 ,2- 5 dimercaptobenzene, xylylenedithiol and 1 ,3,5-tris(3- mercaptopropyl) isocyanurate.

In the thermally dissociating shell-forming resin used in the present invention, at least 30%, preferably at least 50 of all of the linkages formed from isocyanate or • _] 0 isothiocyanate groups are thermally dissociating linkages. When the content of the thermally dissociating linkages is less than 30%, the strength of the shell in the heat-and- pressure fixing cannot be sufficiently lowered, making it less likely to exhibit any advantageous fixing performance ,,- of the core material.

In the thermally dissociating encapsulated toner of the present invention, other compounds having an isocyanate- reactive functional group other than phenolic hydroxyl and thiol groups, which may be used as a shell-forming material 0 in such an amount as not to lower the ratio of the linkages formed by the reaction of isocyanate and/or isothiocyanate groups with phenolic hydroxyl and/or thiol groups to the all of the linkages formed from isocyanate and/or isothiocyanate groups is less than 30%, include, for 5 example, the following active methylene compounds such as malonate and acetoacetate, oxime such as methyl ethyl ketone oxime, carboxylic acid, polyol, polyamine, aminocarboxylic acid and aminoalcohol.

According to the present invention, the compound having one active hydrogen atom reactive with isocyanate and/or isothiocyanate groups as the component (3) may be used in an amount of at most 30 mol % based on the active hydrogen component. When the amount exceeds 30 mol %, the storage stability of the resulting toner is undesirably poor.

Further, the molar ratio of (A) the isocyanate compound and/or isothiocyanate compound comprising the components (1) and (2) to (B) the active hydrogen compounds comprising the components (3) and (4) preferably lies between 1:1 and 1:20 in order to obtain a resin free from unreacted isocyanate groups.

In the production of the encapsulated toner according to the present invention, the shell is preferably formed by an interfacial polymerization or an in-situ polymerization. Alternatively, it may be formed by a dry method comprising stirring in an air stream at a high rate matrix particles used as a core material together with particles used as a shell-forming material having a number-average particle size of one-eighth or less of that of the matrix particles.

The resins to be used as the shell materials can be produced in the presence of no catalysts; however, when the resins are produced in the presence of catalysts, those catalysts including tin catalysts such as dibutyltindilaurate, etc., amine catalysts such as 1 ,4-diazabicyclo[2.2.2]octane, N,N,N-tris- (dimethylaminopropyl)-hexahydro-S-triazine, etc. and any known urethane catalysts can be used.

The resins to be used as core materials of the encapsulated toner according to the present invention are thermoplastic resins having glass transition points (Tg) of 10 to 50°C , and examples thereof include polyester resins, polyester-polyamide resins, polyamide resins and vinyl resins, among which vinyl resins are particularly preferable. When the glass transition point (Tg) is less than 10°C , the storage stability of the resulting encapsulated toner is undesirably poor, and when it exceeds 50°C , the fixing strength of the encapsulated toner is undesirably poor.

Examples of the monomers constituting the vinyl resins include styrene and its derivatives such as styrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, a -methylstyrene, p-ethylstyrene, 2,4-dimethylstyrene, p-chlorostyrene and vinylnaphthalene; ethylenically unsaturated monoolefins such as ethylene, propylene, butylene and isobutylene; vinyl esters such as vinyl chloride, vinyl bromide, vinyl fluoride, vinyl acetate, vinyl propionate, vinyl formate and vinyl caproate; ethylenic monocarboxylic acids and esters thereof such as acrylic acid, methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, tert-butyl acrylate, amyl acrylate, cyclohexyl acrylate, n-octyl acrylate, isooctyl acrylate, decyl acrylate, lauryl acrylate, 2-ethylhexyl acrylate, stearyl acrylate, methoxyethyl acrylate, 2-hydroxyethyl acrylate, glycidyl acrylate, 2-chloroethyl acrylate, phenyl acrylate,

methyl a -chloroacrylate, methacrylic acid, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, tert-butyl methacrylate, amyl methacrylate, cyclohexyl methacrylate, n-octyl methacrylate, isooctyl methacrylate, decyl methacrylate, lauryl methacrylate, 2-ethylhexyl methacrylate, stearyl methacrylate, methoxyethyl methacrylate, 2-hydroxyethyl methacrylate, glycidyl methacrylate, phenyl methacrylate, dimethylaminoethyl methacrylate and diethylaminoethyl methacrylate; ethylenic monocarboxylic acid derivatives such as acrylonitrile, methacrylonitrile and acrylamide; ethylenic dicarboxylic acids and derivatives thereof such as dimethyl aleate; vinyl ketones such as vinyl methyl ketone; vinyl ethers such as vinyl methyl ether; vinylidene halides such as vinylidene chloride; and N-vinyl compounds such as N-vinylpyrrole and N-vinylpyrrolidone.

Among the above core material resin-constituting monomers according to the present invention, the core material-forming resin contains, in the main skeleton of the resin, styrene or its derivatives preferably in an amount of 50 to 90 parts by weight, and the ethylenic monocarboxylic acid or an ester thereof preferably in an amount of 10 to 50 parts by weight to control the thermal properties of the resin, such as the softening point.

When the monomer composition constituting the core material-forming resin according to the present invention contains a crosslinking agent, which may be also used, if

necessary, as a mixture of two or more of .them, any known crosslinking agents may be properly used. When the amount of the crosslinking agent added is too large, the resulting toner is less likely to be heat-fused, thereby resulting in poor heat fixing ability and heat-and-pressure fixing ability. On the contrary, when the amount is too small, in heat-and-pressure fixing, a part of the toner cannot be completely fixed on a paper but rather adheres to the surface of a roller, which in turn is transferred to a subsequent paper which creates the so-called "offset" or "offset phenomenon." Accordingly, the amount of the crosslinking agent is preferably 0.001 to 15% by weight, more preferably 0.1 to 10% by weight, based on the monomers used. The core material of the thermally dissociating encapsulated toner according to the present invention may further contain, if necessary, one or more offset inhibitors of any known kind for the purpose of improving offset resistance at heat-and-pressure fixing. These offset inhibitors are contained in an amount of 1 to 20% by weight based on the resin contained in the core material.

The core material of the thermally dissociating encapsulated toner according to the present invention contains a coloring agent, which may be any one of the dyes and pigments used in the conventional toners. The coloring agent is generally contained in an amount of 1 to 15 parts by weight per 100 parts by weight of the resin contained in the core material.

In addition, in the shell-forming materials of the thermally dissociating encapsulated toner according to the present invention and in the core material, a metal- containing dye which has been used for toners, for example, a metal complex of an organic compound having a carboxyl or nitrogenous group, such as nigrosine, may be added in an effective amount as a charge control agent. Alternatively, such a charge control agent may be mixed with the toner.

The thermally dissociating encapsulated toner according to the present invention may contain, if necessary, a fluidity improver and/or a cleanability improver. Further, for the purpose of controlling the developability of the encapsulated toner, an additive, for example, finely powdered polymethyl methacrylate, etc. may be added. Furthermore, for the purposes of toning or resistance control, a small amount of carbon black may be used.

The thermally dissociating encapsulated toner of the present invention preferably has a softening point of not less t n 80°C and not more than 150°C . If the softening point is lower than 80°C , the offset resistance of the resulting encapsulated toner is undesirably poor, and when it exceeds 150°C , the fixing strength of the encapsulated toner is undesirably poor.

Although the particle size of the encapsulated toner according to the present invention is not particularly limited, the average particle size thereof is generally 3 to 30 _# m. The preferred thickness of the shell of the encapsulated toner is from 0.01 to 1 μ. m. When the thickness

is less than 0.01 ^ m, the blocking resistance of the resulting encapsulated toner is poor, and when it exceeds 1#m, the heat fusibility of the resulting encapsulated toner is undesirably poor. Examples of the thermally dissociating encapsulated toners which is preferably used in the present invention are described above, but the present invention is not confined to these alone.

The method of forming fixed images of the present invention are detailed below, referring to the drawings. Figure 1 is a schematic view of an apparatus used for the method of forming fixed images as defined by the present invention. Element 1 is a photoconductor such as of amorphous silicon or organic photoconductor, etc. in which a photoconductive layer is provided on a conductive supporter. For photoconductors, those practically used are photoconductors of selenium, silicon, organic groups, etc., and any of these can be used. Element 7 is a charger located opposite to the photoconductor 1. The charging means is not particularly restricted, and any of, for example, a corona charger, a brush charger, a roller charger, etc. can be used. Element 2 is an exposure device located opposite to the photoconductor 1 for forming electrostatic latent images on the photoconductor surface. For an exposure device 2, light sources such as laser beams, LED or EL arrays, etc. are used in combination with an image-forming optical system. Alternatively, a device based on optical systems projecting a reflected light of a

document usually provided in the copying machine can be used. Element 3 is a developer device located opposite to the photoconductor 1 for making visible the electrostatic latent image formed on the photoconductor with the toner. For a developer device, any of the commonly used two- component magnetic brush developer devices, the one- component magnetic brush developer device, and the one- component non-magnetic developer device, etc. can be used. The toners to be used in the present invention are thermally dissociating encapsulated toners, which are produced by an interfacial polymerization method, etc.

The toner applied to the electrostatic latent image formed on the photoconductor is transferred by the transfer device 5b to the recording medium 6. Known as transfer methods are a corona transfer method, wherein corona ions are supplied to the reverse side of the recording medium; a roller transfer method, wherein a transfer electric field is formed by voltage generated by pressing a conductive roller, to which a voltage is applied, against the reverse side of the recording medium; and an induction belt transfer method, wherein an inductive belt serves to convey the recording medium, etc., and all of these methods are applicable to the present invention.

The cleaner device 8 such as a cleaning web for removing trace amounts of the toner remaining on the photoconductor after the transfer process is placed opposite to the photoconductor 1.

In the fixing process, the toner transferred onto the

recording medium is first preheated by an endless heating film. As long as the heating film can heat the toner on the recording medium to a temperature of up to 120°C , there are no limitations on the materials used therefor. For instance, those generally known as heating sheets can be used. Examples include those obtained by dispersing a conductive material such as conductive carbon, conductive inorganic powders, conductive whiskers of potassium titanate, etc. into a resin such as a polyamide resin, a polyamide-imide resin, a polycarbonate resin, etc., and thus molding into a formed body (Japanese Patent Laid- Open Nos. 10592/1977, 23740/1977 and 5795/1978).

In addition, those obtained by producing a circuit pattern on an insulating releasing layer using metal foils of aluminum, nickel, stainless steel, nichrome, etc. as a resistance heating element by such methods as photoetching, pressing, printing, etc. so as to meet specific requirements for temperature characteristics can be used (Japanese Patent Laid-Open Nos. 90243/1973, 90245/1973 and 115343/1974). Among those mentioned above, those blends of the conductive materials or those capable of freely adjusting the heating temperature by a circuit pattern and thus generating far infrared radiation are preferred heating elements for an endless heating film in the present invention, because they have remarkably good heating efficiency, small energy consumption and fast temperature- rising speed. Examples thereof include, for instance, a heating element described in Japanese Patent Laid-Open No.

19889/1981. In addition, those having PTC characteristics (Positive Thermo Conductivity: As the temperature increases, the resistivity increases.) can adjust their own temperature, thus making it more preferred heating elements. Examples thereof include, for instance, those heating elements described in Japanese Patent Laid-Open Nos. 10592/1977, 5795/1978 and 14034/1979).

Figure 8 shows a schematic cross-sectional view of one example of a heating film. The heating film comprises a fluorine resin film (an insulating releasing layer lid) of 75 μ, m in thickness; an aluminum deposition layer (a conductive layer 11c) formed on the fluorine resin film; a heating layer 11b comprising a thermoplastic resin dispersed with conductive carbon forπed on the surface of the aluminum deposition layer; and an aluminum foil (a conductive layer 11a) formed on the heating layer 11b, whereby the heating layer 11b is laminated with the conductive layers 11a and 11c to construct a sandwich-like structure. In addition, heat in the heating film can be generated by connecting terminals to each of two conductive layers (11a and 11c), and conducting electricity. The heating film can be heated quickly up to a desired temperature by adjusting the resistivity in the heating layer and applied voltage. Alternatively, as shown in Figure 9, it is also possible to use a heating film produced by laminating the heating layer 11b and the insulating releasing layer lid. In this case, terminals 11e and 11f are arranged to contact with the heating layer lib, and the

effective length between those terminals is normally 20 to 400 mm, preferably 40 to 200 mm.

As shown in Figures 7 and 9, the endless heating film comprising the above heating film is stretched with at least one pair of rollers, for example, a fixing roller (a pressure roller) 12a and a holding roller 16. In addition, upon the stretching of the endless heating film, number of rollers can be increased, if necessary. For example, as shown in Figure 10, a stretched endless heating film is used.

The toner to be fixed onto the recording medium is conveyed in parallel with the endless heating film to the fixing portion comprising a pair of the fixing rollers (the pressure rollers) 12a, 12b. For instance, as shown in Figures 1 and 7, the recording medium 6 is conveyed along the surface in parallel with the endless heating film 11 by a conveyor belt 15. The toner adhered onto the recording medium while conveying the recording medium is preheated by the heat transmitted from the endless heating film. In this case, the heating temperature of the endless heating film is properly adjusted based on the conveying speed of the ^* recording medium, so that the preheating temperature of the toner falls within specified temperature ranges.

As a means for pressure-fixing the toner thus preheated onto the recording medium, a pair of fixing rollers

(pressure rollers) can be used. The toner is fixed by inserting the recording medium between the pair of the fixing rollers (the pressure rollers) 12a, 12b through the

endless heating film. Specifically, elements 12a, 12b are fixing rollers (pressure rollers), which are arranged so that the recording medium can be pressed through the endless heating film at a specified nip pressure. Since fixing takes place in the case of ordinary fixing devices at a high temperature (around 200°c ) , expensive heat-resistant silicone rubber, Teflon resin, etc. must be used for the fixing rollers (pressure rollers) 12a, 12b. However, since the surface temperature of the toner preheated by using the endless heating film is at most 120°C in the present invention, the temperature transmitted to the fixing roller is very low. Therefore, a high heat resistance is not required for the fixing roller. Accordingly, as long as it is an elastic member having a softening point of not less than 120°C , there are iio limitations on its material, and any of the ordinary inexpensive elastic materials can be used. For instance, polyester resins, nylon resins, heat- resistant polyurethane resins, heat-resistant synthetic rubbers, etc. can be used. Further, since such a low nip pressure as less than 4 kg/cm is applicable to a fixing device in the present invention, the durability of the fixing roller becomes longer.

A cleaning device such as a cleaning web 8b is arranged in the fixing device for the purpose of removing trace amounts of the toner remaining on the endless heating film after the fixing process. As long as the toner remaining on the endless heating film can be removed, the arranging position of the cleaning web 8b is not particularly limited.

For instance, as shown in Figures 1, 7 and 9, the cleaning web 8b may be arranged opposite to the fixing roller (the pressure roller) 12a. Alternatively, as shown in Figure 10, it may be arranged opposite to the holding roller 16. After fixing process, the recording medium is discharged out of the apparatus by a particular paper discharging means not illustrated in the figure.

The photoconductor 1, the endless heating film 11, the conveyor belt 15, the fixing rollers (the pressure rollers) 12a and 12b and the holding roller 16 are rotated by specified driving means not illustrated in the figures in the direction shown in the respective drawings at specified peripheral speeds.

In general, the toners are fixed by a conventionally known heat roller method. In this method, however, since the nip width cannot be taken widely, the time during which the recording medium contacts the heat roller surface is extremely short, thereby simultaneously supplying heat and pressure in a short period of time. Accordingly, the surface temperature of the heat roller is required to be extremely high. However, in the present invention, the toner transferred onto the recording medium is fixed by being pressed with a fixing roller after sufficiently heating the internal portion of the toner adhered onto the recording medium by preheating using the endless heating film. Therefore, as compared to the conventional heat roller method, fixing of the toner onto the recording medium can take place at an extremely low fixing temperature and a low

nip pressure. Particularly the use of the thermally dissociating encapsulated toner according to the present invention is highly effective, because the shell material is fragile to heat, and thus the core material having a low glass transition point can be fixed.

Next, the individual processes of the method of forming fixed images by the present invention having the above- mentioned construction will be described.

Figure 3 shows a charging process, Figure 4 an exposing process, Figure 5 a developing process, Figure 6 a transfer process and Figures 7 through 10 fixing processes.

In the charging process, as shown in Figure 3, a specified charge is uniformly supplied, e.g. by the corona charger 7 to the photoconductor surface. A photoconductor sensitive to a positive charge is taken here for an example, and the surface of the conductive supporter lb is coated with the photoconductive layer 1a to form the photoconductor 1. A uniform charge is applied by the corona charger 7 to the photoconductive layer la, thereby positively charging the surface of the photoconductive layer 1a.

In the exposing process, as shown in Figure 4, a light from the exposure device 2 is irradiated to the surface of the above photoconductor, so that a leakage of charges occurs only in the exposed parts to form an electrostatic latent image on the photoconductive layer la.

In the developing process, as shown in Figure 5, the toner triboelectrically charged inside the developer device

is transported by the rotating sleeve 3a, and developed onto the photoconductor surface in proportion to the charge on the photoconductor surface. The developing process is an assortment of normal development in which a reversely polarized toner adheres to the charges by the Coulomb's force and of reverse development in which the toner adheres to the charges lost due to exposure to the light. The development process in the present invention applies to either method, but the case of the normal development is illustrated in Figure 5.

In the transfer process, as shown in Figure 6, the visible image formed on the photoconductor surface accepts the charges from the reverse side of the recording medium 6 such as the recording paper through a transfer-corotron or a transfer-roller, and it is then transferred to the recording medium 6. Part of the toner is left behind untransferred on the photocionductor surface, which is removed by the cleaning device 8 such as a cleaning web arranged opposite to the photoconductor as shown in Figure 1. In the fixing process, as shown in Figures 1 and 7, while the recording medium 6 is conveyed along the surface of the endless heating film 11 by a means of the conveyor belt 15, the visible image transferred onto the recording medium 6 is heated in advance by the heat transmitted from the endless heating film 11, and then the surface of the recording medium onto which the visible image is adhered is pressure-welded to the surface of the endless heating film by a pair of the fixing rollers (the pressure rollers) 12a

and 12b, thereby strongly fixing the visible image onto the recording medium 6.

In the present invention, the toner on the recording medium is heated in the process of conveying within the temperature range of normally between 40°C and 120°C , preferably between 60°C and 120°C . When the heating temperature is less than 40°C , the melting of the toner becomes insufficient, and when it exceeds 120°C , the fixing temperature becomes too high, posing problems incurred by the conventional methods as mentioned above. In the case of the conventional methods, the nip pressure in the fixing process has to be made higher, if the fixing temperature is made lower, thereby requiring a nip pressure of usually not less than 4 kg/cm. However, in the present invention, although the fixing temperature is set to be not more than 120°C , a sufficient fixing strength can be obtained with a nip pressure of normally 0.5 to 4 kg/cm, and even less than 2 kg/cm in many cases. Therefore, fixing can take place at a low nip pressure, thereby making the durability of the fixing roller longer. Moreover, in general, if the temperature applied to the surface of the recording medium is too high, the recording paper tends to curl. If the temperature is too low, the fixing of the toner becomes insufficient, making record pj servation difficult. Therefore, since the fixing can be carried out in the temperature range of 40°C to 120°C in the present invention as mentioned above, such problems are not likely to take place.

ϊn addition, the toner remaining on the surface of the endless heating film after fixing process is removed by cleaning means such as a cleaning web 8b, so that the endless heating film can be repeatedly used. On the other hand, the charges remaining on the photoconductor 1 after the developing process and the transfer process are over are neutralized by a charge eraser 9 such as a charge erasing lamp into a reusable state again for the charging process. — In addition, the present invention is not confined to the above-mentioned embodiments, and specifications of the kinds of individual apparatus, processes etc. can be revised based on the principles of the present invention.

By using the method of forming fixed images of the present invention, the following effects can be obtained:

(1) Since the pressure-fixing is carried out after preheating the toner, fixing takes place at a low temperature.

(2) Since the fixing is carried out at a fixing temperature of not more than 120°C , the fixing apparatus can be simplified, making it possible to miniaturize the fixing device and lower the cost.

(3) Since the fixing is carried out at a fixing temperature of not more than 120°C , heat-resistant members which have been required for the conventional devices are not required for the fixing device and the periphery thereof in the present invention, making it possible to use less expensive materials and lower the cost.

(4) ^' Since the fixing is carried out at a fixing temperature of not more than 120°C with a low nip pressure, paper sheets become less likely to curl or jam, and thus conserving in its maintenance. (5) Since the fixing is carried out at a fixing temperature of not more than 120°C with a lower nip pressure, durability of the components of the fixing device and the periphery thereof becomes longer, and thus conserving in its maintenance. (6) Since a toner for the low-temperature fixing is used, the temperature of the heating element in the fixing device can be set low with only a small rise of the temperature in the printing machine. Accordingly, a forced radiation device such as an electric fan can be made smaller or is not required, thereby reducing the noise problem.

(7) Since the waiting time for the temperature rise in the fixing device can be shortened, quick printing is made possible.

The present invention is hereinafter described in more detail by means of the following working examples, but the present invention is not limited by them. Production Example of Encapsulated Toner:

To a mixture comprising 70.0 parts by weight of tyrene, 30.0 parts by weight of 2-ethylhexyl acrylate and ..0 part by weight of divinylbenzene, 10.0 parts by weight of carbon black "#44" (manufactured by Mitsubishi Chemical Industries, Ltd.), 4.0 parts by weight of 2,2'- azobisisobutyronitrile, 9.5 parts by weight of 4,4'-

diphenylmethane diisocyanate "Millionate MT" (manufactured by Nippon Polyurethane Industry Co., Ltd.) are added. The obtained mixture is introduced into an attritor (manufactured by Mitsui Miike Kakoki) and dispersed at 10°C for 5 hours to give a polymerizable composition. This composition is added to 800 g of a 4% by weight aqueous colloidal solution of tricalcium phosphate which had been preliminarily prepared in a 2-liter separable glass flask, so as to give a concentration of 30% by weight. The obtained mixture is emulsified and dispersed with a TK homomixer (manufactured by Tokushu Kika Kogyo) at 5°C and a rotational speed of 10000 rpm for 2 minutes. A four-necked glass cap is set on the flask, and a reflux condenser, a thermometer, a dropping funnel fitted with a nitrogen inlet tube and a stainless steel stirring rod are set thereon. The resulting flask is placed on an electric mantle heater. A solution of 22.0 g of resorcinol, 3.6 g of diethyl malonate and 0.5 g of 1 ,4-diazabicyclo[2.2.2]octane in 40 g of ion-exchanged water is prepared, and the resulting mixture is dropped into the flask in a period of 30 minutes through the dropping funnel while stirring. Thereafter, the contents are heated to 80°c and reacted for 10 hours in a nitrogen atmosphere while stirring. After cooling the reaction mixture, it is dissolved into 10%-aqueous hydrochloric acid. The resulting mixture is filtered and the obtained solid is washed with water, dried under a reduced pressure of 20 mmHg at 45°C for 12 hours and classified with an air classifier to give the encapsulated toner with an average particle size of 9 μ m

having a shell made of a resin having a thermally dissociating urethane linkage. The glass transition point assignable to the resin contained in the core material is 30.2°C, and its softening point is 130.0°C. Production Example of Reference Toner:

To 100 parts by weight of a polyester resin (Bisphenol- type polyester resin; softening point: 135°C ; Tg: 65°C), 7 parts by weight of carbon black (manufactured by Mitsubishi Kasei Ltd., MA8), 3 parts by weight of a polypropylene wax (Sanyo Kasei Ltd., Biscol 660P), and 2 parts by weight of a charge control agent (Hodogaya Kagaku Ltd., Aizenspilon Black TRH) are mixed, and the resulting mixture is kneaded by a pressurized kneader. After sufficiently dispersing the obtained mixture, it is pulverized with a pulverizing mill and then classified with a classifier to obtain a toner having a particle distribution range of 5 to 25 μ m and an average particle size of 10 m. To 1 kg of the toner, 5 g of colloidal silica (Ninon Aerozil Ltd.: R972) is externally added to obtain a surface-treated reference toner.

Test Example 1 :

50 g of the toner obtained in Production Example of Encapsulated Toner is blended together with 1 kg of a commercially available ferrite carrier by using a V-type blender to obtain a developer 1. The obtained developer 1 is loaded on a commercially available copying machine to develop images without fixing. The fixing ability and the non- offsetting region of the toner of the present invention are

measured using the fixing device of the present invention schematically shown in Figure 7 (roller diameter: 20m φ ; nip pressure: 1.0 kg/cm; effective length of heating film: 50 mm), while varying the heating temperature at a linear velocity of 20 mm/sec. As a result, the lowest fixing temperature is 80 ^C C , and the non-offsetting region of the toner is at a temperature between 70°C and 180°C •

On the other hand, the toner obtained by the Production Example of Reference Toner is mixed with a commercially available ferrite carrier to prepare a developer 2. After developing images in the same manner as above using a commercially available copying machine, the fixing ability and the non-offsetting region of the reference toner are measured using the fixing device of the present invention. As a result, the lowest fixing temperature is 125°C , and the non-offsetting region of the toner is at a temperature between 100°C and 180°C. Test Example 2:

The developer 1 obtained in Test Example 1 is loaded on a commercially available copying machine to develop images without fixing. The fixing ability and the non-offsetting region of the toner of the present invention are measured using a conventional fixing device schematically shown in Figure 2 (roller diameter: 30mm φ ; nip pressure: 2.0 kg/cm; an aluminum surface of the heat roller being surface-coated with Teflon in a thickness of 50 μ m; the pressure roller being heat-resistant silicone rubber roll), while varying the heating temperature at a linear velocity of 20 mm/sec.

As a result, the lowest fixing temperature is 100°C , and the non-offsetting region of the toner is at a temperature between 80°C and 200°C •

On the other hand, by using the developer 2 obtained in the Test Example 1 , developing images are obtained in the same manner as above using a commercially available copying machine. After that, the fixing ability and the non- offsetting region of the reference toner are measured using the same fixing device as above. As a result, the lowest fixing temperature is 135°C , and the non-offsetting region of the toner is at a temperature between 115°C and 200°C •

The lowest fixing temperature for the toner is the temperature of the paper surface at which the fixing rate of the toner exceeds 70%. This fixing rate of the toner is determined by placing a load of 500 g on a sand-containing rubber eraser having a bottom area of 15 mm x 7.5 mm which contacts the fixed toner image, placing the loaded eraser on a fixed toner image obtained in the fixing device, moving the loaded eraser on the image backward and forward five i-imes, measuring the optical reflective density of the aser-treated image with a reflective densitometer manufactured by Macbeth Co., and then calculating the fixing rate from this density value and a density value before the eraser treatment using the following equation.

Image density after eraser treatment

Fixing rate = x 100

Image density before eraser treatment

From these test examples, it is confirmed that by

utilizϊng the method of forming fixed images according to the present invention, the lowest fixing temperature can be remarkably lowered when compared to the case where the conventional heat roller-type fixing device is used. This is particularly remarkably effective in a case where a thermally dissociating encapsulated toner is used.

The present invention being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention, and all such modifications as would be obvious to one skilled in the art are intended to be included within the scope of the following claims.