Patent Application
20190204774
The present invention relates to an image forming apparatus and a developer set.
In electrophotography, an electrostatic charge image formed on a surface of an image holding member (photoreceptor) is developed using a developer including toner to form a toner image, and the obtained toner image is transferred to a recording medium and fixed with a heating roller or the like, thereby obtaining an image.
According to an aspect of the invention, there is provided a developer set including: a first developer and a second developer. The first developer includes a first toner and a first carrier. The second developer includes a second toner and a second carrier. The second toner is a toner that includes a flaky brilliant pigment, a toner that includes a white pigment, or a transparent toner. The second carrier has a higher volume resistivity than the first carrier and has a larger volume average particle diameter than the first carrier.
Exemplary embodiment(s) of the present invention will be described in detail based on the following figures, wherein:
Hereinafter, an exemplary embodiment which is an example of the invention will be described in detail.
An image forming apparatus and an image forming method according to the exemplary embodiment will be described.
An image forming apparatus according to the exemplary embodiment includes: a first image forming unit; and a second image forming unit that is disposed downstream of the first image forming unit in a traveling direction of a transfer medium.
Hereinafter, the image forming unit will also be simply referred to as “unit”. In addition, the downstream side in the traveling direction of the transfer medium will also be referred to as “downstream side”, and the upstream side in the traveling direction of the transfer medium will also be referred to as “upstream side”.
The first unit includes: a first image holding member; and a first developing unit that develops an electrostatic charge image formed on a surface of the first image holding member using a first developer to form a toner image on the surface of the first image holding member. In addition, the second unit includes: a second image holding member; and a second developing unit that develops an electrostatic charge image formed on a surface of the second image holding member using a second developer to form a toner image on the surface of the second image holding member.
The first developing unit accommodates the first developer that includes a first toner and a first carrier, and the second developing unit accommodates the second developer that includes a second toner and a second carrier.
In addition, the image forming apparatus according to the exemplary embodiment includes: a first transfer unit that transfers the toner image, which is formed on the surface of the first image holding member by the first developing unit, to the transfer medium; and a second transfer unit that transfers the toner image, which is formed on the surface of the second image holding member by the second developing unit, to the transfer medium to which the first toner image is transferred.
In the image forming apparatus according to the exemplary embodiment, a volume resistivity of the first carrier is lower than a volume resistivity of the second carrier, and a volume average particle diameter of the first carrier is less than a volume average particle diameter of the second carrier.
In addition, the image forming method according to the exemplary embodiment includes: a first image forming step of forming a first electrostatic charge image on a surface of the first image holding member, developing the first electrostatic charge image using the first developer including the first toner and the first carrier to forma first toner image on the surface of the first image holding member, and transferring the first toner image to the transfer medium in the first unit; and a second image forming step of forming a second electrostatic charge image on a surface of the second image holding member, developing the second electrostatic charge image using the second developer including the second toner and the second carrier to form a second toner image on the surface of the second image holding member, and transferring the second toner image to the transfer medium to which the first toner image is transferred in the second unit.
In the image forming method according to the exemplary embodiment, a volume resistivity of the first carrier is lower than a volume resistivity of the second carrier, and a volume average particle diameter of the first carrier is less than a volume average particle diameter of the second carrier.
Here, “image forming unit” is an image forming unit including at least an image holding member and a developing unit, and the image forming unit may further include at least one selected from the group consisting of a charging unit, an electrostatic charge image forming unit, and a cleaning member that cleans an image holding member.
“Transfer medium” described herein refers to a medium to which a toner image formed on a surface of an image holding member is transferred. For example, the transfer medium is a recording medium in a direct transfer type apparatus in which a toner image formed on a surface of an image holding member is directly transferred to a recording medium. In addition, the transfer medium is an intermediate transfer member in an intermediate transfer type apparatus in which a toner image formed on a surface of an image holding member is primarily transferred to a surface of an intermediate transfer member, and the toner image transferred to the surface of the intermediate transfer member is secondarily transferred to a surface of a recording medium.
In addition, the second unit that is “disposed downstream of the first image forming unit in the traveling direction of the transfer medium” is a unit that is disposed downstream of the first unit among plural units that are disposed along the traveling direction of the transfer medium.
In the exemplary embodiment, one first unit or plural first units may be used. That is, in the image forming apparatus including plural first units, the first carrier accommodated in each of the plural first units has a lower volume resistivity than the second carrier and has a smaller volume average particle diameter than the second carrier. In addition, the image forming apparatus including plural first units includes the same number of first transfer units as that of the first units.
In addition, the image forming apparatus may further include units other than the first unit and the second unit (for example, a unit that is disposed upstream of the first unit or a unit that is disposed downstream of the second unit).
In the image forming apparatus according to the exemplary embodiment, the volume resistivity of the first carrier accommodated in the first unit is lower than that of the second carrier accommodated in the second unit, and the volume average particle diameter of the first carrier is less than that of the second carrier. Therefore, formation of a white line which may occur on an image formed after continuous formation of low-density images may be suppressed, as compared to a case where the volume resistivity of the first carrier is lower than that of the second carrier and the volume average particle diameter of the first carrier is the same as that of the second carrier.
The reason is not clear but is presumed to be as follows.
Recently, a demand not only for formation of an image using toners of the related art including a yellow toner, a magenta toner, a cyan toner, and a black toner but also for formation of an image using special color toners such as a brilliant toner, a white toner, and a transparent toner has increased.
A carrier used in combination with the special color toners is designed according to characteristics or use of the toners. Therefore, a carrier having different characteristics (for example volume resistivity) from a carrier used in combination with the toners of the related art may be used.
Specifically, for example, a brilliant toner including a flaky brilliant pigment or a white toner including a white pigment includes a conductive pigment. Therefore, the volume resistivity is likely to be lower than that of the toners of the related art. Thus, as a carrier used in combination with the brilliant toner or the white toner, a carrier having a higher volume resistivity than the carrier of the related art is used.
In addition, for example, a transparent toner (that is, a toner including no colorants or 1.0% by mass or lower of a colorant with respect to the amount of toner particles) is used for forming a thick toner image in many cases from the viewpoint of, for example, forming a transparent film. Therefore, the transparent toner is used in combination with a carrier having a higher volume resistivity than the carrier of the related art.
Due to the above-described reason, for example, in the image forming apparatus in which a developer including the special color toner and a developer including the toner of the related art are accommodated in developing units of respective units, the volume resistivities of the carriers accommodated in the units are different from each other.
In addition, not only in the special color toners but also in the toners of the related art including a yellow toner, a magenta toner, a cyan toner, and a black toner, carriers having different volume resistivities may be used in a case where, for example, characteristics or uses of the toners are different.
Due to the above-described reasons, in the image forming apparatus including plural image forming units, for example, the first unit that accommodates the first developer including the first carrier having a relatively low volume resistivity and the second unit that accommodates the second developer including the second carrier having a relatively high volume resistivity may be used in combination.
In a case where the first unit and the second unit are disposed along the traveling direction of the transfer medium, for example, the first toner image formed by the first unit is transferred to the transfer medium, and then the second toner image formed by the second unit is transferred to the transfer medium.
At this time, in a case where the first carrier (that is, the carrier having a relatively low volume resistivity) accommodated in the first unit is incorporated into the first toner image, the first carrier may be incorporated into the second developing unit of the second image forming unit through the first toner image of the transfer medium.
The incorporation of the carrier will be described in detail.
First, in a case where the first carrier is incorporated into the first toner image formed on the first image holding member of the first unit, the first toner image including the first carrier is transferred from the first image holding member to the transfer medium by the first transfer unit. In a case where the second toner image formed on the second image holding member is transferred to the transfer medium by the second transfer unit, the first carrier included in the first toner image formed on the transfer medium may be transferred to the second image holding member and incorporated into the second developing unit.
In a case where the second unit includes a cleaning member that cleans the second image holding member, a part of the first carrier transferred to the second image holding member is removed by the cleaning member. However, the other part of the first carrier may pass through the cleaning member without being removed, may reach the second developing unit, and may be incorporated into the second developer. In particular, in a case where the cleaning member is a blade cleaning type cleaning member including a cleaning blade, in a case the posture of the cleaning blade is unstable, the first carrier is likely to pass through the cleaning blade. The posture of the cleaning blade is unstable in a case where the supply amount of a toner is small, for example, a case where non-paper-feeding portions are continuously provided or a case where low-density images are continuously formed.
While the first carrier incorporated into the second developing unit is moving, for example, an external additive such as silica particles in the toner or a release agent component in toner particles is physically adsorbed on a surface of the carrier, and thus the resistance locally increases. Therefore, in a case where the toner is released from the first carrier that is incorporated into the second developing unit has a locally high resistance, charges having a polarity opposite to that of the toner are likely to remain on a surface of the first carrier. In a case where the first carrier in which the charges having a polarity opposite to that of the toner remains on the surface is transported to a developing sleeve in the second developing unit, due to an electrostatic force of the charges included in the first carrier, the second toner may be removed from the second toner image that is formed on the second image holding member in the developing step. In particular, in a low-temperature and low-humidity environment, a developer is likely to have a high resistance and high chargeability. Therefore, the above-described phenomenon is likely to occur.
A portion where the second toner is removed causes “formation of a white line” or “a decrease in density” to occur on a finally obtained image.
On the other hand, in the exemplary embodiment, the volume resistivity of the first carrier is lower than the volume resistivity of the second carrier, and the volume average particle diameter of the first carrier is less than the volume average particle diameter of the second carrier.
In a developer accumulation portion of the developing unit before a layer restriction member, the developer is agitated and charged. A carrier having a large diameter also has a high magnetic binding force, and thus is preferentially transported from the developer accumulation portion to a surface of a developing roller (hereinafter, also referred to as “developing sleeve”). That is, even in a case where the first carrier is incorporated into the second developing unit, the second carrier is preferentially transported to the developing sleeve. On the other hand, the incorporated first carrier has a small diameter. Therefore, the first carrier accumulates in the developer accumulation portion and densely exchanges charges with the toner. This way, the first carrier having a small diameter incorporated into the second developing unit densely exchanges charges with the toner. Therefore, even in a case where charges having a polarity opposite to the toner remains on a surface, charges on the surface are neutralized. As a result, it is presumed that, even in a case where the first carrier having a small diameter is supplied to the developing sleeve in the second developing unit, formation of a white line or a decrease in density may be suppressed.
This way, it is presumed that formation of a white line, which may occur on an image formed after continuous formation of low-density images, is suppressed.
As the image forming apparatus according to the exemplary embodiment, various well-known image forming apparatuses may be used, the apparatuses including: a direct transfer type apparatus in which a toner image formed on a surface of an image holding member is directly transferred to a recording medium; an intermediate transfer type apparatus in which a toner image formed on a surface of an image holding member is primarily transferred to a surface of an intermediate transfer member, and the toner image transferred to the surface of the intermediate transfer member is secondarily transferred to a surface of a recording medium; an apparatus including a cleaning unit that cleans a surface of an image holding member after a toner image is transferred and before charging; and an apparatus including an erasing unit that irradiates a surface of an image holding member with erasing light for erasing charges after a toner image is transferred and before charging.
The intermediate transfer type apparatus includes: an intermediate transfer member having a surface to which a toner image is transferred; a primary transfer unit that primarily transfers a toner image, which is formed on a surface of an image holding member, to the surface of the intermediate transfer member; and a secondary transfer unit that secondarily transfers the toner image, which is transferred to the surface of the intermediate transfer member, to a surface of a recording medium. In this case, as the primary transfer unit, the first transfer unit and the second transfer unit are used.
In the image forming apparatus according to the exemplary embodiment, for example, a portion of each of the units including the developing unit may have a cartridge structure (process cartridge) which is detachable from the image forming apparatus.
Hereinafter, the image forming apparatus according to the exemplary embodiment will be described using, as an example, an intermediate transfer type apparatus in which a toner image formed on a surface of an image holding member is primarily transferred to a surface of an intermediate transfer member, and the toner image transferred to the surface of the intermediate transfer member is secondarily transferred to a surface of a recording medium. However, the image forming apparatus is not limited to the intermediate transfer type apparatus. Major components shown in the drawings will be described, and the other components will not be described.
As an example of the image forming apparatus according to the exemplary embodiment, an intermediate transfer type image forming apparatus will be described, in which a tandem type configuration including plural image forming units is adopted, a brilliant toner is used as the special color toner, and an intermediate transfer belt is provided as an intermediate transfer member which is a transfer medium.
In the image forming apparatus shown in
The image forming units 50Y, 50M, 50C, 50K, and 50B are disposed in this order from the upstream side in a rotating direction of an intermediate transfer belt 33.
Here, the image forming units 50Y, 50M, 50C, 50K, and 50B have the same configuration, except for the colors of the toners in the developers accommodated therein. Therefore, here, the image forming unit 50Y that forms a yellow image will be described as a representative example. The same components as those of the image forming unit 50Y are represented by reference numerals to which the symbols M (magenta) , C (cyan) , K (black) , and silver (B) are attached instead of the symbol Y (yellow), and the image forming units 50M, 50C, 50K, and 50B will not be described.
Here, in the image forming apparatus shown in
In addition, the image forming unit 50B disposed on the most downstream side corresponds to the second unit. A developing device 20B (that is, the second developing unit) of the unit 50B accommodates the second developer that includes a brilliant toner corresponding to the second toner and includes the second carrier having a relatively high volume resistivity and having a relatively large volume average particle diameter.
As the first developer and the second developer, although not particularly limited, a first developer and a second developer constituting a developer set described below are preferably used, respectively. The details of the first developer and the second developer will be described below.
Here, the units 50Y, 50M, 50C, 50K, and 50B have the same configuration, except for the colors of the toners in the developers accommodated therein. Therefore, here, the unit 50Y that forms a yellow image will be described as a representative example.
Photoreceptors 21Y, 21M, 21C, and 21K as image holding members that are included in the units 50Y, 50M, 50C, and 50K, respectively, correspond to the first image holding member, toner images that are formed by the units 50Y, 50M, 50C, and 50K, respectively, correspond to the first toner image, and primary transfer rollers 17Y, 17M, 17C, and 17K that transfer the first toner images to the intermediate transfer belt 33, respectively, correspond to the first transfer unit.
In addition, a photoreceptor 21B as an image holding member that is included in the unit 50B corresponds to the second image holding member, a toner image that is formed by the unit 50B corresponds to the second toner image, and a primary transfer roller 17B that transfers the second toner image to the intermediate transfer belt 33 corresponds to the second transfer unit.
The same components as those of the unit 50Y are represented by reference numerals to which the symbols M (magenta), C (cyan), K (black) , and silver (B) are attached instead of the symbol Y (yellow) , and the units 50M, 50C, 50K, and 50B will not be described.
The yellow image forming unit 50Y includes the photoreceptor 21Y as the image holding member, and the photoreceptor 21Y is rotated by a driving unit (not shown) at a predetermined process speed in a direction indicated by arrow A in the drawing. As the photoreceptor 21Y, for example, an organic photoreceptor having sensitivity to an infrared range is used.
A charging roller (charging unit) 28Y is provided above the photoreceptor 21Y, a predetermined voltage is applied to the charging roller 28Y by a power supply (not shown), and a surface of the photoreceptor 21Y is charged to a predetermined potential.
In the vicinity of the photoreceptor 21Y, an exposure device (electrostatic charge image forming unit) 19Y that exposes a surface of the photoreceptor 21Y to form an electrostatic charge image thereon is disposed downstream of the charging roller 28Y in a rotating direction of the photoreceptor 21Y. Here, as the exposure device 19Y, an LED array capable of realizing reduction in size is used due to limitation in space, but the exemplary embodiment is not limited thereto. However, an electrostatic charge image forming unit using another laser beam or the like may be used.
In addition, in the vicinity of the photoreceptor 21Y, the developing device (developing unit) 20Y including a developer holding member that holds a yellow developer is disposed downstream of the exposure device 19Y in the rotating direction of the photoreceptor 21Y, an electrostatic charge image formed on the surface of the photoreceptor 21Y is developed by a yellow toner, and a toner image is formed on the surface of the photoreceptor 21Y.
The intermediate transfer belt (transfer medium, primary transfer unit) 33 to which the toner image formed on the surface of the photoreceptor 21Y is primarily transferred is disposed below the photoreceptor 21Y so as to extend across a region below the five photoreceptors 21Y, 21M, 21C, 21K, and 21B. The intermediate transfer belt 33 is pressed toward the surface of the photoreceptor 21Y by the primary transfer roller 17Y. In addition, the intermediate transfer belt 33 is stretched by three rollers including a drive roller 22, a support roller 23, and a bias roller 24, and moves in a direction indicated by arrow B at the same moving speed as the process speed of the photoreceptor 21Y. The yellow toner image is primarily transferred to a surface of the intermediate transfer belt 33, and toner images of respective colors including magenta, cyan, black, and silver (brilliance) are further sequentially primarily transferred thereto and layered.
In addition, in the vicinity of the photoreceptor 21Y, a cleaning device 15Y that cleans the toner remaining on the surface of the photoreceptor 21Y or the toner retransferred thereto is disposed downstream of the primary transfer roller 17Y in the rotating direction of the photoreceptor 21Y (direction indicated by arrow A) . As the cleaning device 15Y, a blade cleaning type device is used. A cleaning blade of the cleaning device 15Y is attached and pressed to a surface of the photoreceptor 21Y in a counter direction.
A material of the cleaning blade is not particularly limited, and various elastomers are used. Specific examples of the elastomer include a polyurethane elastomer, silicone rubber, and chloroprene rubber.
As the polyurethane elastomer, in general, polyurethanes that are synthesized through an addition reaction of isocyanate, polyol, and various hydrogen-containing compounds are used. Specifically, the polyurethane elastomer is manufactured by preparing a urethane prepolymer using a polyol component and an isocyanate component, adding a curing agent to the urethane prepolymer, injecting the compound into a mold, crosslinking and curing compound, and aging the cured product at a normal temperature (25° C.). In this case, examples of the polyol component include: an ether polyol such as polypropylene glycol or polytetramethylene glycol; an adipate polyol; a polycaprolactam polyol; and a polyester polyol such as a polycarbonate polyol. Examples of the isocyanate component include: an aromatic polyisocyanate such as tolylene diisocyanate, 4,4′-diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanate, or tolidine diisocyanate; and an aliphatic polyisocyanate such as hexamethylene diisocyanate, isophorone diisocyanate, xylylene diisocyanate, or dicyclohexylmethane diisocyanate. As the curing agent, typically, a dihydric alcohol such as 1,4-butanediol and a trihydric or higher polyhydric alcohol such as trimethylolpropane or pentaerythritol are used in combination.
In a case where a rubber hardness (according to durometer Type A of JIS K 6253-3:2012) of the cleaning blade is 50° or higher, the cleaning blade is not likely to be worn. Therefore, the toner is not likely to pass through the cleaning blade.
In a case where the rubber hardness is 100° or lower, the cleaning blade is not excessively hard. Therefore, the wearing of the image holding member is not likely to progress, and cleaning performance is not likely to deteriorate.
In addition, in a case where a 300% modulus, which shows a tensile stress at a sample elongation of 300%, is 80 kgf/cm2 or higher, a blade edge is likely to be deformed and is not likely to be torn off. The cleaning blade has resistance to chipping or wearing, and the toner is not likely to pass through the cleaning blade. On the other hand, in a case where the 300% modulus is 550 kgf/cm2 or lower, deterioration in followability with respect to a surface shape of the image holding member, which is caused by deformation of the cleaning blade, is not likely to occur. Therefore, cleaning failure caused by contact failure is not likely to occur.
Further, in the cleaning blade in which a rebound resilience defined by a rebound test method of JIS K 6255:1996 (hereinafter, simply referred to as “rebound resilience”) is 4% or higher, a reciprocating motion of the blade edge scraping the toner is likely to occur. Therefore, the toner is not likely to pass through the cleaning blade. In addition, in the cleaning blade in which the rebound resilience is 85% or lower, blade squeal or blade turned-up is not likely to occur.
In addition, the amount of biting of the cleaning blade (the amount of the cleaning blade deformed by being pressed against the surface of the image holding member) is not unconditionally determined and is preferably from 0.8 mm to 1 . 6 mm and more preferably from 1.0 mm to 1.4 mm. Further, a contact angle between the cleaning blade and the image holding member (an angle between the cleaning blade and a tangent line of the surface of the image holding member) is not unconditionally determined and is preferably from 18° to 28°.
A secondary transfer roller (secondary transfer unit) 34 is pressed against the bias roller 24, which stretches the intermediate transfer belt 33, through the intermediate transfer belt 33. In a nip portion between the bias roller 24 and the secondary transfer roller 34, the toner image primarily transferred and layered on the surface of the intermediate transfer belt 33 is electrostatically transferred to a surface of a recording sheet (recording medium) P supplied from a sheet cassette (not shown). At this time, since the silver toner image is positioned on the uppermost side (uppermost layer) among the toner images transferred and layered on the intermediate transfer belt 33, the silver toner image is positioned on the lowermost side (lowermost layer) among the toner images transferred to the surface of the recording sheet P.
Here, although not particularly limited, it is preferable that the intermediate transfer belt 33 includes a polyimide resin or a polyamide imide resin from the viewpoints of obtaining high strength of the intermediate transfer belt 33 itself and satisfying durability thereof. In addition, a surface resistivity of the intermediate transfer belt 33 is, for example, preferably from 1×109 Ω/sq to 1×1014 Ω/sq. In order to control the surface resistivity, the intermediate transfer belt 33 optionally includes a conductive filler. As the conductive filler, one kind or a combination of two or more kinds selected from the following group may be used, the group including: a metal or an alloy such as carbon black, graphite, aluminum, or a copper alloy; a metal oxide such as tin oxide, zinc oxide, potassium titanate, a tin oxide-indium oxide complex oxide, or a tin oxide-antimony oxide complex oxide; and a conductive polymer such as polyaniline. Among these, for example, carbon black is preferable as the conductive filler from the viewpoint of costs. In addition, a processing auxiliary agent such as a dispersant or a lubricant is optionally added.
In addition, a fixing unit 35 that fixes the toner images, which are transferred and layered on the recording sheet P, on the surface of the recording sheet P by heat and pressure to form a permanent image is disposed downstream of the secondary transfer roller 34 (the path is not shown).
Examples of the fixing unit 35 include: a fixing belt having a belt shape in which a surface is formed of a low surface energy material such as a fluororesin component or a silicone resin; and a fixing roller having a cylindrical shape in which a surface is formed of a low surface energy material such as a fluororesin component or a silicone resin.
The image forming apparatus shown in
Next, operations of the units 50Y, 50M, 50C, 50K, and 50B that form color images of yellow, magenta, cyan, black, and silver (brilliance) will be described. The operations of the units 50Y, 50M, 50C, 50K, and 50B are the same, and thus the operation of the yellow unit 50Y will be described as a representative example.
In the yellow unit 50Y, the photoreceptor 21Y rotates in the direction indicated by arrow A at a predetermined process speed. A surface of the photoreceptor 21Y is negatively charged to a predetermined potential by the charging roller 28Y. Next, the surface of the photoreceptor 21Y is exposed by the exposure device 19Y to form an electrostatic charge image corresponding to image information. Next, the negatively charged toner is reversely developed by the developing device 20Y, the electrostatic charge image formed on the surface of the photoreceptor 21Y is visualized on the surface of the photoreceptor 21Y, and a toner image is formed. Next, the toner image formed on the surface of the photoreceptor 21Y is primarily transferred to a surface of the intermediate transfer belt 33 by the primary transfer roller 17Y. After the primary transfer, a transfer remaining component such as the toner remaining in the surface of the photoreceptor 21Y is scraped and cleaned by the cleaning blade of the cleaning device 15Y for the next image forming step.
The above-described operations are performed by the units 50Y, 50M, 50C, 50K, and 50B. The toner images visualized on the surfaces of the photoreceptors 21Y, 21M, 21C, 21K, and 21B are sequentially transferred and layered on a surface of the intermediate transfer belt 33. In a color mode, the toner images of the respective colors are transferred and layered in order of yellow, magenta, cyan, black, and silver (brilliance) . In addition, in a two-color or three-color mode, only toner images of necessary colors are transferred or transferred and layered. Next, the toner images transferred or transferred and layered on the surface of the intermediate transfer belt 33 are secondarily transferred to a surface of the recording sheet P by the secondary transfer roller 34, the recording sheet P being transported from the sheet cassette (not shown). Next, the toner images are fixed by being heated and pressed by the fixing unit 35. The toner remaining on the surface of the intermediate transfer belt 33 after the secondary transfer is removed by a belt cleaner 26 constituting the cleaning blade for the intermediate transfer belt 33.
In addition, charges of the intermediate transfer belt 33 to which the toner image are transferred or transferred and layered are erased by the drive roller 22.
In the image forming apparatus shown in
In the image forming apparatus shown in
In the image forming apparatus shown in
The image forming apparatus according to the exemplary embodiment is not limited to the above-described configuration. The disposition order is not limited to the above-described configuration as long as the second unit is disposed downstream of the first unit.
In addition, in the image forming apparatus shown in
In the image forming apparatus shown in
The first carrier accommodated in the first unit is highly likely to be incorporated into the second developing unit of the second unit adjacent to the first unit. Therefore, although not particularly limited, it is preferable that the first unit and the second unit are adjacent to each other as in the image forming apparatus shown in
In the image forming apparatus shown in
In the image forming apparatus shown in
In the unit 50Y of the image forming apparatus shown in FIG. 1, the developing device 20B including a developer holding member that holds a silver (brilliance) developer, the photoreceptor 21B, the charging roller 28B, and the cleaning device 15B are integrated into a process cartridge that is detachable from the image forming apparatus main body. In addition, the units 50M, 50C, 50K, and 50B are also configured as process cartridges, respectively, as in the case of the unit 50Y.
A configuration of the process cartridge will be described below.
A process cartridge 200 shown in
In
The process cartridge is not limited to the above-described configuration, and may include the developing device and optionally at least one component selected from other units such as an image holding member, a charging unit, an electrostatic charge image forming unit, and a transfer unit.
The developer set includes: a first developer that includes a first toner and a first carrier; and a second developer that includes a second toner and a second carrier, the second carrier having a higher volume resistivity than the first carrier and having a larger volume average particle diameter than the first carrier.
Here, in the developer set according to the exemplary embodiment, the second toner is a toner that includes a flaky brilliant pigment, a toner that includes a white pigment, or a transparent toner.
The developer set may include plural first developers or may further include other developers.
A mixing ratio (mass ratio; toner:carrier) of the toner to the carrier in the each of developers varies depending on the kinds of the toner and the carrier to be used and is not particularly limited, and is preferably 1:100 to 30:100 and more preferably 3:100 to 20:100.
Hereinafter, the details of the carriers (that is, the first carrier and the second carrier) used in the developer set according to the exemplary embodiment will be described.
The first carrier and the second carrier are not particularly limited as long as magnitude relationships of the volume resistivity and the volume average particle diameter satisfy the above-described conditions, and well-known carriers of the related art may be used. For example, a carrier including core particles and a resin coating layer that coats the core particles may be used.
In the carriers (that is, the first carrier and the second carrier) used in the developer set according to the exemplary embodiment, for example, it is preferable that the volume resistivities are from 1×106 Ωcm to 1×1014 Ωcm from the viewpoint of obtaining a high-quality image. The volume resistivity of the second carrier is higher than that of the first carrier.
Here, the volume resistivities of the carriers are volume resistivities at 20° C. and are measured using the following method.
The developer in the developing device is separated into the toner and the carrier by air blowing to extract the carrier therefrom. The separation between the toner and the carrier by air blowing is repeated.
Next, the extracted carrier is placed flat on a surface of a circular jig on which a 20 cm2 electrode plate is disposed such that the thickness thereof is from 1 mm to 3 mm, thereby forming a layer. Another 20 cm2 electrode plate is disposed on the layer such that the layer is interposed between the electrode plates. In order to remove a gap in a measurement target, a load of 4 kg is applied to the electrode plate disposed above the layer, and then the thickness (cm) of the layer is measured. Both of the electrodes disposed above and below the layer are connected to an electrometer and a high-voltage power supply. A high voltage is applied to both the electrodes so as to generate an electric field of 103.8 V/cm, and a current value (A) flowing at this time is read. The measurement environment is an applied voltage of 1000 V, a temperature of 20° C., and a humidity of 50% RH. An expression of calculating the volume electric resistance (Ωcm) of the measurement target is as follows.
R=E×20/(I−I0)/L
In the above expression, R represents the volume electric resistance (Ωcm) of the measurement target, E represents the applied voltage (V), I represents the current value (A), I0 represents the current value (A) at an applied voltage of 0 V, and L represents the thickness (cm) of the layer. The coefficient 20 represents the area (cm2) of the electrode plates.
The volume resistivity of the second carrier is, for example, preferably from 3.2 times to 50000 times, more preferably from 10 times to 45000 times, and still more preferably from 100 times to 40000 times with respect to the volume resistivity of the first carrier.
By adjusting a ratio (the volume resistivity of the second carrier/the volume resistivity of the first carrier) to be in the above-described range, carrier scattering caused by charge injection may be suppressed as compared to a case where the ratio is lower than the above-described range, and density unevenness caused by a small development field may be suppressed as compared to a case where the ratio is higher than the above-described range.
The volume resistivity of the second carrier is, for example, preferably from 1×106 Ωcm to 1×1014 Ωcm, more preferably from 1×107 Ωcm to 1×1012 Ωcm, and still more preferably from 1×107 Ωcm to 1×109 Ωcm.
In a case where the developer set includes plural first developers, for example, it is preferable that the above-described preferable range is applied to all the first carriers.
For example, in a case where each of the carriers is a carrier including core particles and a resin coating layer, the volume resistivity of the carrier is controlled by adjusting, for example, the kind of core particles, the resin coating amount of the resin coating layer described below, the content of conductive particles in the resin coating layer, or a combination thereof described below.
In either the first carrier or the second carrier, the resin coating amount of the resin coating layer is, for example, 0.5% by mass or higher with respect to the total mass of the carrier (preferably from 0.7% by mass to 6.0% by mass and more preferably from 1.0% by mass to 5.0% by mass).
As the resin coating amount of the resin coating layer increases, the volume resistivity of the carrier increases. Therefore, in a case where the volume resistivity of the carrier is controlled by adjusting the resin coating amount of the resin coating layer, for example, the resin coating amount of the first carrier is larger than that of the second carrier.
The resin coating amount of the resin coating layer is obtained as follows.
In the case of a resin coating layer that is soluble in a solvent, a carrier that is accurately weighed is dissolved in a solvent (for example, toluene or N-methylpyrrolidone) in which the resin coating layer is soluble, the core particles are held with a magnet, and the solution in which the resin coating layer is dissolved is drained away. By repeating this operation several times, core particles from which the resin coating layer is removed remain. The mass of the core particles after being dried is measured, and then the difference is divided by the amount of a carrier to calculate the coating amount.
Specifically, 20.0 g of a carrier is weighed and put into a beaker, 100 g of toluene is added thereto, and the mixture is stirred with a stirring blade for 10 minutes. A magnet is placed under the bottom of the beaker, and the toluene is drained away such that the core particles do not flow out. This operation is repeated four times, and the beaker after the toluene is drained away is dried. The amount of the magnetic particles after the drying is measured, and the coating amount is calculated from the expression “ (Carrier Amount-Amount of Core Particles After Washing)/Carrier Amount”.
On the other hand, in the case of a coating layer that is insoluble in a solvent, a carrier is heated in a nitrogen atmosphere in a range of from room temperature (25° C.) to 1,000° C. using a Thermo plus EVO II differential thermogravimetric analyzer TG 8120 (manufactured by Rigaku Corporation). The resin coating amount is calculated from a decrease in the mass of the carrier.
In a case where the resin coating layer includes conductive particles, the content of the conductive particles in the resin coating layer is, for example, from 0.1% by mass to 50% by mass, preferably from 0.15% by mass to 20% by mass, and more preferably from 0.2% by mass to 10% by mass.
As the content of the conductive particles in the resin coating layer increases, the volume resistivity of the carrier decreases. Therefore, in a case where the volume resistivity of the carrier is controlled by adjusting the content of the conductive particles in the resin coating layer, for example, the content of the conductive particles in the resin coating layer of the first carrier is lower than (or 0% by mass) that of the conductive particles in the resin coating layer of the second carrier.
In the carriers (that is, the first carrier and the second carrier) used in the developer set according to the exemplary embodiment, it is preferable that the volume average particle diameters are, for example, from 20 μm to 100 μm. The volume average particle diameter of the second carrier is more than that of the first carrier.
Here, the volume average particle diameters of the carriers are measured using the following method. The volume average particle diameter of the core particles is also measured as follows.
Using a laser scattering diffraction particle diameter distribution analyzer (LS particle diameter analyzer, manufactured by Beckman Coulter Co., Ltd.), a particle diameter distribution is measured. As an electrolytic solution, ISOTON-II (manufactured by Beckman Coulter Co., Ltd.) is used. The number of particles to be measured is 50,000.
Using the measured particle diameter distribution, a volume cumulative particle diameter distribution is drawn on divided particle diameter ranges (channels) from the smallest particle diameter. A particle diameter having a cumulative value of 50% by volume (also referred to as “D50v”) is defined as “volume average particle diameter”.
The volume average particle diameter of each of the carriers is obtained by performing the above-described measurement on the carrier that is extracted after separating the developer in the developing device into the toner and the carrier by air blowingair blowing.
The volume average particle diameter of the second carrier is, for example, preferably from 1.1 times to 2.0 times, more preferably from 1.2 times to 1.9 times, and still more preferably from 1.4 times to 1.8 times with respect to the volume average particle diameter of the first carrier.
By adjusting a ratio (the volume average particle diameter of the first carrier/the volume average particle diameter of the second carrier) to be in the above-described range, the formation of a white line is more likely to be suppressed as compared to a case where the ratio is lower than the above-described range, and unevenness in image density caused by an unstable state of a magnetic brush formed on the developing sleeve is suppressed as compared to a case where the ratio is higher than the above-described range.
The volume average particle diameter of the second carrier is, for example, preferably from 20 μm to 100 μm, more preferably from 25 μm to 40 μm, and still more preferably from 30 μm to 35 μm.
In a case where the developer set includes plural first developers, for example, it is preferable that the above-described preferable range is applied to all the first carriers.
For example, in a case where each of the carriers is a carrier including core particles and a resin coating layer, the volume average particle diameter of the carrier is controlled by adjusting, for example, the volume average particle diameter of the core particles, the thickness of the resin coating layer, or a combination thereof.
Hereinafter, common configurations of the first carrier and the second carrier will be described.
Examples of the core particles according to the exemplary embodiment include magnetic metal particles (for example, particles of iron, steel, nickel, or cobalt), magnetic oxide particles (for example, particles of ferrite or magnetite), and magnetic particle-dispersed resin particles in which the above particles are dispersed in a resin. In addition, examples of the core particles include particles obtained by impregnating porous magnetic particles with a resin.
It is preferable that the core particles are ferrite particles represented by, for example, the following formula.
(MO)X(Fe2O3)Y Formula:
In the formula, Y represents from 2.1 to 2.4, and X represents 3-Y. M represents a metal element. Although not particularly limited, M preferably contains at least Mn as the metal element.
For example, M contains Mn as a major component and may further contain at least one element selected from the group consisting of Li, Ca, Sr, Sn, Cu, Zn, Ba, Mg, and Ti (preferably, the group consisting of Li, Ca, Sr, Mg, and Ti from the viewpoint of the environment).
The core particles are obtained by magnetic granulation or sintering, and as a pre-treatment, the magnetic materials may be pulverized. A pulverization method is not particularly limited. For example, a well-known pulverization method may be used, and specific examples thereof include methods using a mortar, a ball mill, and a jet mill.
The resin contained in the magnetic particle-dispersed resin particles which are the core particles are not particularly limited, and examples thereof include styrene resins, acrylic resins, phenol resins, melamine resins, epoxy resins, urethane resins, polyester resins, and silicone resins. In addition, optionally, other components such as a charge-controlling agent or fluorine-containing particles may be further added to the magnetic particle-dispersed resin particles which are the core particle.
A volume average particle diameter of the core particles is, for example, from 10 μm to 500 μm, and is preferably from 15 μm to 80 μm and more preferably from 20 μm to 60 μm.
In a case where the volume resistivity of the carrier is controlled by adjusting the kind of core particles, for example, the volume resistivity is largely affected by whether or not the core particles are surface-treated.
By performing an oxidation treatment on the core particle, the volume resistivity tends to increase. By using the core particles on which the oxidation treatment is performed, the volume resistivity of the carrier is easily controlled.
In the oxidation treatment, an oxygen concentration, an oxidation temperature, and a heating time are control factors of the volume resistivity. For example, in the oxidation treatment that is performed on the core particles, the volume resistivity of the core particles tends to increase by increasing the oxidation temperature or by increasing the heating time.
Based on the above description, the oxidation treatment is performed on the core particles used in the second carrier, and the oxidation treatment is not performed on the core particles used in the first carrier or is performed at a lower temperature or for a shorter time than that of the core particles of the second carrier such that the two carriers used in the developer set according to the exemplary embodiment are obtained.
Examples of the coating resin of the resin coating layer include acrylic resins, polyethylene resins, polypropylene resins, polystyrene resins, polyacrylonitrile resins, polyvinylacetate resins, polyvinylalcohol resins, polyvinylbutyral resins, polyvinyl chloride resins, polyvinyl carbazole resins, polyvinyl ether resins, polyvinyl ketone resins, vinyl chloride-vinyl acetate copolymers, styrene-acrylic acid ester copolymers, straight silicone resins having an organosiloxane bond and modified compounds thereof, fluororesins, polyester resins, polyurethane resins, polycarbonate resins, phenol resins, amino resins, melamine resins, benzoguanamine resins, urea resins, amide resins, and epoxy resins.
The resin coating layer may further contain resin particles for the purposes of charge control and the like, or may further contain conductive particles for the purposes of resistance control and the like. The coating layer may further include other additives.
The resin particles are not particularly limited. For example, a charge-controlling material is preferable, and examples thereof include melamine resin particles, urea resin particles, urethane resin particles, polyester resin particles, and acrylic resin particles.
Examples of the conductive particles include carbon black particles, various metal powders, and metal oxide particles (for example, particles of titanium oxide, tin oxide, magnetite, and ferrite). Among these, one kind may be used alone, or two or more kinds may be used in combination. Among these, for example, carbon black particles are preferably used from the viewpoints of manufacturing stability, cost, conductivity, and the like. The kind of the carbon black is not particularly limited. For example, carbon black having a DBP absorption of, approximately, from 50 ml/100 g to 250 ml/100 g is preferably used from the viewpoint of manufacturing stability.
A method of forming the resin coating layer on the surfaces of the core particles is not particularly limited, and a well-known method may be adopted. Examples of the method include a dipping method in which a resin coating layer-forming solution is prepared, and the core particles are dipped in the resin coating layer-forming solution; a spray method in which a resin coating layer-forming solution is sprayed on the surfaces of the core particles; a fluidized bed method in which a resin coating layer-forming solution is sprayed on the core particles while floating the core particles with flowing air; a kneader coater method in which the core particles and a resin coating layer-forming solution are mixed in a kneader coater, and then a solvent is removed; and a powder coating method in which the core particles and resin powder are heated and mixed. Further, after being formed, the resin coating layer may be heated using a device such as an electric furnace or a kiln.
Regarding the magnetic force of the carrier, the saturation magnetization at a magnetic field of 1000 oersted may be, for example, 40 emu/g or higher or 50 emu/g or higher.
Here, the saturation magnetization of the carrier is measured using a vibrating sample magnetometer VSMP10-15 (manufactured by Toei Industry Co., Ltd.). A measurement sample is put into a cell having an internal diameter of 7 mm and a height of 5 mm, and the cell is set to the device. In the measurement, a magnetic field is applied to the sample and is swept to 3,000 oersted at a maximum. Next, the applied magnetic field is reduced to prepare a hysteresis curve on a recording sheet. Based on this curve data, the saturation magnetization is obtained.
The first toner and the second toner are not particularly limited, and compositions and physical properties thereof are the same as or different from each other.
The second toner is a brilliant toner, a white toner, or a transparent toner. Therefore, the first toner is, for example, a yellow toner, a magenta toner, a cyan toner, or a black toner which is easily used in combination with a carrier having a relatively low volume resistivity and having a relatively small volume average particle diameter.
Dielectric loss tangents of the first toner and the second toner are not particularly limited, and it is preferable that the dielectric loss tangent of the second toner is higher than that of the first toner.
That is, although not particularly limited, it is preferable that the first developer that includes the first toner having a relatively low dielectric loss tangent and the first carrier having a relatively high resistance and a relatively large particle diameter is used in combination with the second developer that includes the second toner having a relatively high dielectric loss tangent and the second carrier having a relatively low resistance and a relatively small particle diameter.
The dielectric loss tangent of the toner varies depending on the composition of the toner or the dispersed state of a colorant. In particular, the dielectric loss tangent of the toner largely depends on the kind of a colorant to be used. For example, in the case of a brilliant toner in which a brilliant pigment is used as a colorant and a white toner in which a white pigment is used as a colorant, the dielectric loss tangent is more likely to be higher than those of the other toners (for example, a yellow toner, a magenta toner, a cyan toner, a black toner, and a transparent toner).
Here, the dielectric loss tangent (tans) of the toner is expressed as a ratio of an imaginary part ε″ to a real part ε′ in “complex dielectric constant ε=ε′−iε” (i represents an imaginary unit) , and is expressed by “dielectric loss tangent (tanδ)=ε”/ε′.
The dielectric loss tangent (tanδ) of the toner is obtained as follows. For example, 5 g of a toner as a measurement target is molded into a pellet (diameter: 50 mm) using a pressure molding machine, and the pellet is seasoned in an environment of 20° C. and 50% RH for 17 hours. Next, the dielectric loss tangent is measured using an LCR meter (LCR meter 6440A, manufactured by Toyo Corporation) in an environment of 20° C. and 50% RH under conditions of frequency: 1 kHz and voltage: 5 V.
The dielectric loss tangent of the second toner is, for example, preferably from 1.5 times to 5.0 times, more preferably from 1.8 times to 4.5 times, and still more preferably from 2.0 times to 3.7 times with respect to the dielectric loss tangent of the first toner.
In addition, the dielectric loss tangent of the second toner is, for example, preferably from 30×10−3 to 70×10−3, more preferably from 40×10−3 to 65×10−3, and still more preferably from 45×10−3 to 65×10−3.
In a case where the developer set includes plural first developers, for example, it is preferable that the above-described preferable range is applied to all the first toners.
Hereinafter, the details of the first toner and the second toner will be described.
First, a general toner (for example, a yellow toner, a magenta toner, a cyan toner, or a black toner) which may be preferably used as the first toner will be described.
The toner includes toner particles and optionally further contains an external additive.
The toner particles include, for example, a binder resin and optionally further contains a colorant, a release agent, and other additives.
Examples of the binder resin include vinyl resins made of a homopolymer of one monomer or copolymers of two or more monomers selected from the following monomers: styrenes (for example, styrene, parachlorostyrene, and a-methylstyrene); (meth)acrylates (for example, methyl acrylate, ethyl acrylate, n-propyl acrylate, n-butyl acrylate, lauryl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, lauryl methacrylate, and 2-ethylhexyl methacrylate); ethylenically unsaturated nitriles (for example, acrylonitrile and methacrylonitrile); vinyl ethers (for example, vinyl methyl ether and vinyl isobutyl ether); vinyl ketones (vinyl methyl ketone, vinyl ethyl ketone, and vinyl isopropenyl ketone); and olefins (for example, ethylene, propylene, and butadiene).
Examples of the binder resin include non-vinyl resins such as epoxy resins, polyester resins, polyurethane resins, polyamide resins, cellulose resins, polyether resins, and modified rosins; mixtures of the non-vinyl resins and the vinyl resins; and graft polymers obtained by polymerization of vinyl monomers in the presence of the non-vinyl resins.
Among these binder resins, one kind may be used alone, two or more kinds may be used in combination.
The content of the binder resin is, for example, preferably from 40% by mass to 95% by mass, more preferably from 50% by mass to 90% by mass, and still more preferably from 60% by mass to 85% by mass with respect to the total amount of the toner particles.
Examples of the colorant include various kinds of pigments such as carbon black, chrome yellow, Hansa Yellow, Benzidine Yellow, Threne Yellow, Quinoline Yellow, Pigment Yellow, Permanent Orange GTR, Pyrazolone Orange, Vulcan Orange, Watchung Red, Permanent Red, Brilliant Carmine 3B, Brilliant Carmine 6B, Du Pont Oil Red, Pyrazolone Red, Lithol Red, Rhodamine B Lake, Lake Red C, Pigment Red, Rose Bengal, Aniline Blue, Ultramarine Blue, Calco Oil Blue, Methylene Blue Chloride, Phthalocyanine Blue, Pigment Blue, Phthalocyanine Green, and Malachite Green Oxalate; and various dyes such as acridine dyes, xanthene dyes, azo dyes, benzoquinone dyes, azine dyes, anthraquinone dyes, thioindigo dyes, dioxazine dyes, thiazine dyes, azomethine dyes, indigo dyes, phthalocyanine dyes, aniline black dyes, polymethine dyes, triphenylmethane dyes, diphenylmethane dyes, and thiazole dyes.
Among these colorants, one kind may be used alone, two or more kinds may be used in combination.
Optionally, the colorant may be surface-treated, or may be used in combination with a dispersant. In addition, plural kinds of colorants may be used in combination.
The content of the colorant is, for example, preferably from 1% by mass to 30% by mass and more preferably from 3% by mass to 15% by mass with respect to the total amount of the toner particles.
Examples of the release agent include hydrocarbon waxes; natural waxes such as carnauba wax, rice wax, and candelilla wax; synthetic or mineral and petroleum waxes such as montan wax; and ester waxes such as fatty acid ester and montanic acid ester. The release agent is not limited to these examples.
The melting temperature of the release agent is, for example, preferably from 50° C. to 110° C. and more preferably from 60° C. to 100° C.
The melting temperature is calculated from the DSC curve obtained from differential scanning calorimetry (DSC) according to a “melting peak temperature” described in a method of calculating melting temperature in “Testing methods for transition temperatures of plastics” of JIS K 7121-1987.
The content of the release agent is, for example, preferably from 1% by mass to 20% by mass and more preferably from 5% by mass to 15% by mass with respect to the total amount of the toner particles .
Examples of the other additives include various additives such as a magnetic material, a charge-controlling agent, and inorganic powder. These additives are included in the toner particles as internal additives.
The toner particles may have a single-layer structure or a so-called core-shell structure including: a core (core particle) and a coating layer (shell layer) that coats the core.
Here, it is preferable that the toner particles having a core-shell structure include, for example, a core that includes a binder resin and optionally further includes other additives such as a colorant and a release agent; and a coating layer that includes a binder resin.
The volume average particle diameter (D50 v) of the toner particles is, for example, preferably from 2 μm to 10 μm and more preferably from 4 μm to 8 μm.
Various average particle diameters and various particle diameter distribution indices of the toner particles are measured by using Coulter MULTISIZER II (manufactured by Beckman Coulter Inc.) as a measuring device and using ISOTON-II (manufactured by Beckman Coulter Co., Ltd.) as an electrolytic solution.
During this measurement, from 0.5 mg to 50 mg of a measurement sample is added to 2 ml of an aqueous solution containing 5% of a surfactant (preferably, sodium alkylbenzene sulfonate) as a dispersant. This solution is added to 100 ml to 150 ml of the electrolytic solution.
The electrolytic solution in which the measurement sample is suspended is dispersed with an ultrasonic disperser for 1 minute. Then, a particle diameter distribution of particles having a particle diameter in a range of from 2 μm to 60 μm is measured using COULTER MULTISIZER II and an aperture having an aperture size of 100 μm. The number of particles to be sampled is 50000.
Using the measured particle diameter distribution, volume and number cumulative particle diameter distributions are drawn on divided particle diameter ranges (channels) in order from the smallest particle diameter. In addition, particle diameters having cumulative values of 16% by volume and number are defined as a volume average particle diameter D16v and a number average particle diameter D16p, respectively. Particle diameters having cumulative values of 50% by volume and number are defined as a volume average particle diameter D50v and a number average particle diameter D50p, respectively. Particle diameters having cumulative values of 84% by volume and number are defined as a volume average particle diameter D84v and a number average particle diameter D84p, respectively.
Using these values, a volume average particle diameter distribution index (GSDv) is calculated from (D84v/D16v)1/2 and a number average particle diameter distribution index (GSDp) is calculated from (D84p/D16p)1/2.
An average circularity of the toner particles is, for example, preferably from 0.94 to 1.00 and more preferably from 0.95 to 0.98.
The average circularity of the toner particles is obtained from “(equivalent circle peripheral length)/(peripheral length) [(peripheral length of circle having the same projected area of particle image)/(peripheral length of particle projected image)]”. Specifically, the average circularity is a value measured using the following method.
First, toner particles as a measurement target are collected by suction, a flat flow is formed, and particle images are obtained as still images by instantaneous stroboscopic light emission. The particle images are analyzed using a flow particle image analyzer (FPIA-3000, manufactured by Sysmex Corporation). As a result, the average circularity is obtained. The number of samples for obtaining the average circularity is 3500.
In a case where a toner includes an external additive, the toner (developer) as a measurement target is dispersed in water including a surfactant, and then the external additive is removed by an ultrasonic treatment. As a result, toner particles are obtained.
Examples of the external additive include inorganic particles. Examples of the inorganic particles include SiO2, TiO2, Al2O3, CuO, ZnO, SnO2, CeO2, Fe2O3, MgO, BaO, CaO, K2O, Na2O, ZrO2, CaO·SiO2, K2O·(TiO2)n, Al2O3·2SiO2, CaCO3, MgCO3, BaSO4, and MgSO4.
Surfaces of the inorganic particles as the external additive may be treated with a hydrophobizing agent. The hydrophobization treatment may be performed, for example, by dipping the inorganic particles in a hydrophobizing agent. The hydrophobizing agent is not particularly limited, and examples thereof include a silane coupling agent, silicone oil, a titanate coupling agent, and an aluminum coupling agent. Among these, one kind may be used alone, two or more kinds may be used in combination.
Typically, the amount of the hydrophobizing agent is, for example, from 1 part by mass to 10 parts by mass with respect to 100 parts by mass of the inorganic particles.
Examples of the external additive include resin particles (for example, resin particles of polystyrene, polymethyl methacrylate (PMMA), and melamine resin) and a cleaning aid (for example, particles of metal salts of higher fatty acids such as zinc stearate and fluorine polymers).
The content of the external additive is, for example, preferably from 0.01% by mass to 5% by mass and more preferably from 0.01% by mass to 2.0% by mass with respect to the total amount of the toner particles.
Next, a method of preparing a toner will be described. The toner is obtained by preparing the toner particles and externally adding the external additive to the toner particles.
The toner particles may be prepared using either a dry method (for example, a kneading and pulverizing method) or a wet method (for example, an aggregating and coalescing method, a suspension and polymerization method, or a dissolution and suspension method). The method of preparing the toner particles is not limited to these methods, and a well-known method is adopted.
Among these, for example, an aggregating and coalescing method is preferably used to obtain the toner particles.
Specifically, for example, in a case where toner particles are prepared using the aggregating and coalescing method, the toner particles are prepared through the following processes including: a process (resin particle dispersion preparing process) of preparing a resin particle dispersion in which resin particles which form a binder resin are dispersed; a process (aggregated particle forming process) of forming aggregated particles by aggregating the resin particles (optionally, including other particles) in the resin particle dispersion (optionally in a dispersion in which the resin particle dispersion is mixed with another particle dispersion); and a process (coalescing process) of forming toner particles by heating an aggregated particle dispersion in which the aggregated particles are dispersed to coalesce the aggregated particles.
Toner particles may be prepared through the following processes including: a process of forming second aggregated particles by obtaining an aggregated particle dispersion in which aggregated particles are dispersed, and then further mixing the aggregated particle dispersion with a resin particle dispersion in which resin particles are dispersed so as to attach the resin particles to surfaces of the aggregated particles; and a process of forming toner particles having a core-shell structure by heating a second aggregated particle dispersion in which the second aggregated particles are dispersed to coalesce the second aggregated particles.
Here, after the coalescing process ends, toner particles formed in the solution undergo well-known processes including a washing process, a solid-liquid separation process, and a drying process. As a result, dry toner particles are obtained.
In the washing process, for example, it is preferable that displacement washing using ion exchange water is sufficiently performed from the viewpoint of charging characteristics. In addition, in the solid-liquid separation process, although there is no particular limitation, it is preferable that suction filtration, pressure filtration, or the like is performed from the viewpoint of productivity. In addition, in the drying process, although there is no particular limitation, it is preferable that freeze drying, flash drying, fluidized drying, vibration-type fluidized drying, or the like is performed from the viewpoint of productivity.
The toner is prepared, for example, by adding the external additive to the obtained dry toner particles and mixing them with each other. For example, it is preferable that the mixing is performed using a V blender, HENSCHEL MIXER, or LODIGE MIXER. Further, optionally, coarse particles of the toner are removed, for example, using a vibration sieve or a wind classifier.
Next, a brilliant toner which may be preferably used as the second toner will be described.
Examples of the brilliant toner include a toner including: brilliant toner particles that include a flaky brilliant pigment and a binder resin; and an external additive. The brilliant toner particles optionally include a release agent, a colorant other than the brilliant pigment, and other additives.
Since the details of the binder resin, the external additive, the release agent, the colorant other than the brilliant pigment, and the other additives are as described above regarding the toner (that is, the yellow toner or the like used as the first toner), the description thereof will not be repeated. In addition, the description of the same features as described above regarding the toner will not be repeated.
Examples of the brilliant pigment include a pigment (brilliant pigment) capable of imparting brilliance such as metallic gloss. The brilliant pigment is not particularly limited as long as it has brilliance, and examples thereof include powders of metals such as aluminum (elemental Al), brass, bronze, nickel, stainless steel, or zinc; micas coated with titanium oxide, yellow iron oxide, or the like; flaky inorganic crystal substrates coated with barium sulfate, layered silicate, layered aluminosilicate, or the like; single-crystal plate-like titanium oxides; basic carbonates; bismuth oxychlorides; natural guanines; flaky glass powders; and metal-deposited flaky glass powders.
Among these brilliant pigments, from the viewpoint of mirror reflection intensity, for example, a metal powder is preferable, and aluminum powder is most preferable.
Examples of the brilliant pigment include a flake shape.
The average length of the brilliant pigment in the long axis direction is, for example, preferably from 1 μm to 30 μm, more preferably from 3 μm to 20 μm, and still more preferably from 5 μm to 15 μm.
Although not particularly limited, a ratio (aspect ratio) of the average length of the brilliant pigment in the long axis direction to the average length of the brilliant pigment in the thickness direction, which is 1, is preferably from 5 to 200, more preferably from 10 to 100, and still more preferably from 30 to 70.
The average length and the aspect ratio of the brilliant pigment are measured using the following method. Using a scanning electron microscope (S-4800, manufactured by Hitachi High-Technologies Corporation), images of pigment particles are obtained at a measurement magnification (300 times to 100000 times). In a state where the obtained images of the pigment particles are two-dimensionalized, the lengths of the particles in the long axis direction and the lengths of the particles in the thickness direction are measured, and the average length in the long axis direction and the aspect ratio of the brilliant pigment are calculated.
The content of the brilliant pigment is, for example, preferably from 1 part by mass to 50 parts by mass and more preferably from 15 parts by mass to 25 parts by mass with respect to 100 parts by mass of the brilliant toner particles.
The toner particles may be brilliant toner particles that have a single-layer structure or brilliant toner particles that have a so-called core-shell structure including: a core (core particle) and a coating layer (shell layer) that coats the core.
For example, it is preferable that the brilliant toner particles having a core-shell structure include: a core that includes a brilliant pigment and a binder resin and optionally further includes other additives such as a release agent; and a coating layer that includes a binder resin.
Although not particularly limited, it is preferable that the brilliant toner particles have a flake shape and has a structure in which an average equivalent circle diameter D is longer than an average maximum thickness C. A ratio (C/D) of the average maximum thickness C to the average equivalent circle diameter D is, for example, preferably from 0.001 to 0.500, more preferably from 0.010 to 0.200, and still more preferably from 0.050 to 0.100.
By adjusting the ratio (C/D) to 0.001 or higher, the strength of the brilliant toner may be secured, breakage caused by stress during the formation of an image may be reduced, a decrease in charging characteristics caused by exposure of the pigment may be reduced, and fogging caused by the decrease in charging characteristics may be reduced. On the other hand, by adjusting the ratio (C/D) to 0.500 or lower, satisfactory brilliance may be obtained.
The average maximum thickness C and the average equivalent circle diameter D are measured using the following method.
The brilliant toner particles are placed on a smooth surface and are uniformly dispersed by vibration. 1000 brilliant toner particles are observed using a color laser microscope “VK-9700” (manufactured by Keyence Corporation) at a magnification of 1000 times to measure the maximum thicknesses C and the equivalent circle diameters D of the brilliant toner particles in a top view, and the average values thereof are obtained.
In a case where cross-sections of the brilliant toner particles in a thickness direction are observed, a ratio (by number) of the brilliant pigment particles whose long axis direction has an angle of −30° to +30° with respect to a long axis direction of the cross-sections of the brilliant toner particles to all the observed brilliant pigment particles is, for example, preferably 60% or higher. Further, the ratio is more preferably from 70% to 95% and still more preferably from 80% to 90%.
By adjusting the ratio to 60% or higher, satisfactory brilliance is obtained.
Here, a method of observing the cross-sections of the brilliant toner particles will be described.
The brilliant toner particles are embedded in a bisphenol A liquid epoxy resin and a curing agent to prepare a sample for cutting. Next, using a cutting machine with a diamond knife (for example, an ultramicrotome (Ultracut UCT, manufactured by Leica)) , the sample for cutting is cut at −100° C. to prepare a sample for observation. Using a high-resolution field emission scanning electron microscope (S-4800, manufactured by Hitachi High-Technologies Corporation), the sample for observation is observed at a magnification at which 1 to 10 brilliant toner particles are observed in one field of view.
Specifically, 100 toner particles in cross-sections of the brilliant toner particles (cross-sections in the thickness direction of the toner particles) are observed. Regarding the observed 100 toner particles, the number of brilliant pigment particles whose long axis direction has an angle of −30° to +30° with respect to a long axis direction of the cross-sections of the brilliant toner particles are counted, for example, using an image analysis software such as WinROOF (manufactured by Mitani Corporation) or using an output sample of an observed image and a protractor to calculate the ratio thereof.
“The long axis direction of the cross-sections of the brilliant toner particles” refers to a direction perpendicular to the thickness direction of the brilliant toner particles in which the average equivalent circle diameter D is longer than the average maximum thickness C. In addition, “the long axis direction of the brilliant pigment” refers to a length direction of the brilliant pigment.
The volume average particle diameter of the brilliant toner particles is, for example, preferably from 1 μm to 30 μm and more preferably from 3 μm to 20 μm.
Next, a white toner which may be preferably used as the second toner will be described.
Examples of the white toner include a toner including: white toner particles that include a white pigment and a binder resin; and an external additive. The white toner particles optionally include a release agent and other additives.
Since the details of the binder resin, the external additive, the release agent, and the other additives are as described above regarding the toner (that is, the yellow toner or the like used as the first toner) , the description thereof will not be repeated. In addition, the description of the same features as described above regarding the toner will not be repeated.
The white pigment is not particularly limited as long as it is white, and examples thereof include: an inorganic pigment (for example, titanium oxide, barium sulfate, lead oxide, zinc oxide, lead titanate, potassium titanate, barium titanate, strontium titanate, zirconia, antimony trioxide, lead white, zinc sulfide, or barium carbonate); and an organic pigment (for example, a polystyrene resin, a urea formalin resin, a polyacrylic resin, a polystyrene-acrylic resin, a polystyrene-butadiene resin, or an alkyl bis melamine resin).
In addition, a pigment having a hollow structure may be used. Examples of the pigment having a hollow structure include: a hollow inorganic pigment (for example, hollow silica, hollow titanium oxide, hollow calcium carbonate, hollow zinc oxide, or zinc oxide tubular particles); and hollow organic particles (for example, a styrene resin, an acrylic resin, a styrene-acrylic resin, a styrene-acrylic acid ester-acrylic acid resin, a styrene-butadiene resin, a styrene-methyl methacrylate-butadiene resin, an ethylene-vinyl acetate resin, an acrylic acid-vinyl acetate resin, or an acrylic acid-maleic acid resin).
Further, for example, heavy calcium carbonate, light calcium carbonate, aluminum hydroxide, satin white, talc, calcium sulfate, magnesium oxide, magnesium carbonate, amorphous silica, colloidal silica, white carbon, kaolin, calcined kaolin, delaminated kaolin, aluminosilicate, sericite, bentonite, or smectite may also be used.
Among these, for example, titanium oxide or zinc oxide is preferable as the white pigment.
As the white pigment, one kind may be used alone, or two or more kinds may be used in combination.
Optionally, the white pigment may be surface-treated, or may be used in combination with a dispersant.
It is preferable that the content of the white pigment is, for example, from 10 parts by mass to 50 parts by mass with respect to 100 parts by mass of the white toner particles. In a case where the content of the white pigment is 10 parts by mass or higher, whiteness and covering properties are likely to be exhibited. On the other hand, in a case where the content of the white pigment is 50 parts by mass or lower, the area of an interface between the white pigment and the binder resin does not increase beyond necessity. Therefore, the white toner image is not likely to be destructed, and an effect of suppressing image destruction is likely to be improved.
The content of the white pigment is, for example, preferably from 20 parts by mass to 50 parts by mass and more preferably from 25 parts by mass to 45 parts by mass with respect to 100 parts by mass of the white toner particles.
The number average particle diameter of the white pigment is, for example, from 200 nm to 400 nm. Ina case where the number average particle diameter of the white pigment is from 200 nm to 400 nm, high whiteness and covering properties maybe exhibited. The number average particle diameter of the white pigment is, for example, preferably 250 nm to 400 nm and more preferably 250 nm to 350 nm.
A particle diameter distribution of the white pigment in the toner particles is calculated, for example, as follows.
The white toner is mixed with and embedded in an epoxy resin, and the mixture is kept overnight to be solidified. Next, using an ultramicrotome (Ultracut UCT, manufactured by Leica), a test piece having a thickness of, for example, from 250 nm to 450 nm is prepared.
The obtained test piece is observed using a high-resolution field emission scanning electron microscope (S-4800, manufactured by Hitachi High-Technologies Corporation) to examine the white pigment in the toner particles.
The obtained image is converted into digital data, the digital data is input to an image analysis software (WinROOF, manufactured by Mitani Corporation), and the number average particle diameter of the white pigment in the toner particles is obtained.
Next, a transparent toner (clear toner) which may be preferably used as the first toner will be described.
The transparent toner includes transparent toner particles including no colorants or 1.0% by mass or lower of a colorant with respect to the amount of toner particles.
Examples of the transparent toner include a toner including transparent toner particles and an external additive. The transparent toner particles optionally include a release agent and other additives.
The content of the colorant is, for example, preferably 1.0% by mass or lower, more preferably 0.5% by mass or lower, and most preferably 0% by mass with respect to the total amount of the transparent toner particles in the transparent toner.
Since the details of the binder resin, the external additive, the release agent, and the other additives are as described above regarding the toner (that is, the yellow toner or the like used as the first toner) , the description thereof will not be repeated. In addition, the description of the same features as described above regarding the toner will not be repeated.
Hereinafter, the exemplary embodiment will be described in detail using Examples but is not limited to these examples. In the following description, unless specified otherwise, “part(s)” and “%” represent “part(s) by mass” and “% by mass”.
Mn-Mg ferrite particles (volume average particle diameter: 43 μm): 100 parts
Cyclohexyl methacrylate/methyl methacrylate copolymer: 3 parts (copolymer molar ratio: 95:5)
Toluene: 14 parts
Among the components constituting the carrier composition, the respective components other than the Mn-Mg ferrite particles and glass beads (ϕ1 mm, the same amount as that of toluene) are stirred using a sand mill (manufactured by Kansai Paint Co., Ltd.) at 200 ppm for 30 minutes. As a result, a resin coating layer-forming solution 1 is obtained. Further, the resin coating layer-forming solution 1 and the Mn-Mg ferrite particles are put into a vacuum degassing type kneader, and toluene is removed by distillation. As a result, a carrier coated with a resin is formed. Next, fine powder and coarse powder are removed using an elbow jet. As a result, a carrier 1-1 is obtained.
A carrier 1-2 is obtained using the same preparation method as that of the carrier 1-1, except that Mn-Mg ferrite particle (volume average particle diameter: 33 μm) is used instead of Mn-Mg ferrite particle (volume average particle diameter: 43 μm).
A carrier 1-3 is obtained using the same preparation method as that of the carrier 1-1, except that Mn-Mg ferrite particle (volume average particle diameter: 58 μm) is used instead of Mn-Mg ferrite particle (volume average particle diameter: 43 μm).
A carrier 1-4 is obtained using the same preparation method as that of the carrier 1-1, except that Mn-Mg ferrite particle (volume average particle diameter: 23 μm) is used instead of Mn-Mg ferrite particle (volume average particle diameter: 43 μm).
Mn-Mg ferrite particles (volume average particle diameter: 28 μm): 100 parts
Cyclohexyl methacrylate/methyl methacrylate copolymer: 3 parts (copolymer molar ratio: 95:5)
Carbon black (VXC72, manufactured by Cabot Corporation): 0.3 parts
Toluene: 14 parts
Among the components constituting the carrier composition, the respective components other than the Mn-Mg ferrite particles and glass beads (ϕ1 mm, the same amount as that of toluene) are stirred using a sand mill (manufactured by Kansai Paint Co., Ltd.) at 200 ppm for 30 minutes. As a result, a resin coating layer-forming solution 1 is obtained. Further, the resin coating layer-forming solution 1 and the Mn-Mg ferrite particles are put into a vacuum degassing type kneader, and toluene is removed by distillation. As a result, a carrier coated with a resin is formed. Next, fine powder and coarse powder are removed using an elbow jet. As a result, a carrier 2-1 is obtained.
A carrier 2-2 is obtained using the same preparation method as that of the carrier 2-1, except that Mn-Mg ferrite particle (volume average particle diameter: 33 μm) is used instead of Mn-Mg ferrite particle (volume average particle diameter: 28 μm).
A carrier 2-3 is obtained using the same preparation method as that of the carrier 2-1, except that Mn-Mg ferrite particle (volume average particle diameter: 23 μm) is used instead of Mn-Mg ferrite particle (volume average particle diameter: 28 μm).
A carrier 2-4 is obtained using the same method as that of the carrier 2-1, except that the addition amount of the carbon black is changed from 0.3 parts to 0.9 parts.
The configurations of the prepared carriers, and the values of the volume resistivity and the volume average particle diameter thereof measured using the above-described method are shown in Table 1.
The volume resistivities and the volume average particle diameters of the obtained carriers are measured using the above-described method, and the measurement results are collectively shown in Table 1 below.
Dimethyl adipate: 74 parts
Dimethyl terephthalate: 192 parts
Ethylene oxide adduct of bisphenol A: 216 parts
Ethylene glycol: 38 parts
Tetrabutoxy titanate (catalyst): 0.037 parts
The above-described materials are put into a two-necked flask which is heated and dried. Nitrogen gas is introduced into the container, and then the materials are heated while being kept in an inert atmosphere and stirred. Next, a polycondensation reaction is caused to occur at 160° C. for 7 hours. Next, the container is heated to 220° C. while gradually reducing the pressure to 10 Torr, and is kept at 220° C. for 4 hours. Next, the pressure is returned to normal pressure, 9 parts of trimellitic anhydride is added, the pressure is gradually reduced to 10 Torr again, and the flask is kept at 220° C. for 1 hour. As a result, a polyester resin is obtained. The glass transition temperature (Tg) of the polyester resin is 64° C.
Polyester resin: 160 parts
Ethyl acetate: 233 parts
sodium hydroxide aqueous solution (0.3 N): 0.1 parts
The above-described materials are put into a 1 L separable flask, are heated at 70° C., and are stirred using a THREE-ONE motor (manufactured by Shinto Scientific Co., Ltd.) to prepare a resin mixed solution. Further, 373 parts of ion exchange water is slowly added for phase-transfer emulsification while stirring the resin mixed solution at 90 rpm, and then the solvent is removed. As a result, a resin particle dispersion (solid content concentration: 30%) is obtained.
Flaky aluminum pigment (2173EA, manufactured by Toyo Aluminum K.K.): 100 parts
Anionic surfactant (NEOGEN R, manufactured by Daiichi Kogyo Seiyaku Co. Ltd.): 1.5 parts
Ion exchange water: 900 parts
The above-described materials are mixed and are dispersed using an emulsifying dispersing device (CAVITRON CR1010, manufactured by Pacific Machinery & Engineering Co., Ltd.) for 1 hour. As a result, a brilliant pigment dispersion (solid content concentration: 10%) is obtained.
Carnauba wax (RC-160, manufactured by Toakasei Co., Ltd.): 50 parts
Anionic surfactant (NEOGEN RK, manufactured by Daiichi Kogyo Seiyaku Co. Ltd.): 1.0 part
Ion exchange water: 200 parts
The above-described materials are mixed, are heated to 95° C., and are dispersed using a homogenizer (ULTRA TURRAX T50, manufactured by IKA) . Next, the solution is further dispersed using a Manton-Gaulin high-pressure homogenizer (manufactured by Gaulin) for 360 minutes. As a result, a release agent dispersion (solid content concentration 20%) is obtained. The volume average particle diameter of release agent particles in the release agent dispersion is 230 nm.
Resin particle dispersion: 500 parts (solid content concentration: 30%)
Brilliant pigment dispersion: 350 parts (solid content concentration: 10%)
Release agent dispersion: 50 parts (solid content concentration: 20%)
Nonionic surfactant (IGEPAL CA897): 1.40 parts
The above-described materials are put into a 2 L cylindrical stainless steel container (diameter: 30 cm) and are dispersed using a homogenizer (ULTRA TURRAX T50, manufactured by IKA) for 10 minutes while applying a shearing force at 4000 rpm. Next, 1.75 parts of a 10% polyaluminum chloride aqueous solution is slowly added dropwise, and the materials are dispersed using a homogenizer at a rotating speed of 5000 rpm for 15 minutes to prepare a raw material dispersion.
Next, the raw material dispersion is put into a polymerization tank including a stirrer with two paddles of stirring blades and a thermometer, starts to be heated using a mantle heater while being stirred at a stirring rotating speed of 200 rpm, and is kept at 54° C. for 2 hours. As a result, a first aggregate is formed. At this time, the pH of the raw material dispersion is controlled to be from 2.2 to 3.5 using 0.3 N nitric acid and 1 N sodium hydroxide aqueous solution.
Next, 123 parts of the resin particle dispersion is added to deposit resin particles on a surface of the first aggregate. As a result, a second aggregate is formed. Next, the second aggregate is heated to 56° C. and kept at 56° C. for 2 hours while observing the form and size of the second aggregate using an optical microscope and a MULTISIZER II (manufactured by Beckman Coulter Inc.). Next, the pH is adjusted to increase to 8.0 and the temperature is increased to 67.5° C. such that the second aggregate coalesce. The pH is reduced to 6.0 while keeping the temperature at 67.5° C. After 1 hour, heating is stopped, and cooling is performed at a temperature decrease rate of 0.1° C./min. Next, the particles are sieved through a 20 μm mesh, are repeatedly washed with water, and are dried using a vacuum dryer. As a result, brilliant toner particles are obtained. The volume average particle diameter of the brilliant toner particles is 9 μm.
100 parts of the obtained brilliant toner particles and 1.5 parts of hydrophobic silica (RY50, manufactured by Nippon Aerosil Co., Ltd.) are mixed using a HENSCHEL mixer at a peripheral speed of 33 m/sec for 2 minutes. Next, the mixture is sieved through a vibration sieve having an opening of 45 μm, a toner 2B which is the brilliant toner including the external additive is obtained.
Carbon black: 50 parts
Anionic surfactant: 5 parts
Ion exchange water: 200 parts
The above-described components are mixed, are dispersed with ULTRA TURRAX (manufactured by IKA) for 5 minutes, and are further dispersed in an ultrasonic bath for 10 minutes. As a result, a black colorant particle dispersion K having a solid content of 21% is obtained.
Paraffin wax (HNP-9 manufactured by Nippon Seiro Co. Ltd.): 19 parts
Anionic surfactant (NEOGEN SC, manufactured by Daiichi Kogyo Seiyaku Co. Ltd.): 1 part
Ion exchange water: 80 parts
The above-described components are mixed in a heat-resistant container, are heated to 90° C. for 30 minutes, and are stirred. Next, the molten solution is caused to flow from the bottom of the container to a Gaulin homogenizer, and a circulation operation corresponding to three passes is performed under a pressure condition of 5 MPa. Next, a circulation operation corresponding to three passes is further performed under an increased pressure of 35 MPa. An emulsion obtained as above is cooled to 40° C. or lower in the heat-resistant container. As a result, a release agent particle dispersion 1 is obtained.
Styrene (manufactured by Wako Pure Chemical Industries Ltd.): 30 parts
N-butyl acrylate (manufactured by Wako Pure Chemical Industries Ltd.): 10 parts
β-carboxyethyl acrylate (manufactured by Solvay): 1.3 parts
Dodecanethiol (manufactured by Wako Pure Chemical Industries Ltd.): 0.4 parts
Ion exchange water: 17 parts
Anionic surfactant (DAWFAX manufactured by The Dow Chemical Company): 0.4 parts
Ion exchange water: 40 parts
Anionic surfactant (DAWFAX manufactured by The Dow Chemical Company): 0.05 parts
Ammonium peroxodisulfate (manufactured by Wako Pure Chemical Industries Ltd.): 0.4 parts
The above-described components of the oil phase and the above-described components of the water phase 1 are put into a flask and are stirred and mixed. As a result, a monomer emulsion dispersion is obtained.
The above-described components of the water phase 2 are put into a reaction container, the atmosphere in the container is sufficiently substituted with nitrogen, and the reaction container is heated in an oil bath under stirring until the internal temperature of the reaction system reaches 75° C.
Further, the monomer emulsion dispersion is slowly added dropwise to the inside of the reaction container for 3 hours, and emulsion polymerization is performed. After the completion of the dropwise addition, the polymerization is continued at 75° C. After 3 hours, the polymerization is finished.
The volume average particle diameter D50 v of the obtained resin particles is 250 nm which is measured using a laser diffraction particle diameter distribution analyzer (LA-700, manufactured by Horiba Ltd.).
The glass transition temperature of the resin is 52° C. which is measured using a differential scanning calorimeter (DSC-50, manufactured by Shimadzu Corporation) at a temperature increase rate of 10° C./min.
The number average molecular weight (in terms of polystyrene) is 13,000 which is measured using a molecular weight measuring device (HLC-8020, manufactured by Tosoh Corporation) and THF (tetrahydrofuran) as a solvent.
As a result, a resin particle dispersion 1 having a volume average particle diameter of 250 nm, a solid content of 42%, a glass transition temperature of 52° C., and a number average molecular weight Mn of 13,000 is obtained.
Resin particle dispersion 1: 50 parts
Colorant particle dispersion K: 30 parts
Release agent particle dispersion 1: 40 parts
Polyaluminum chloride: 0.4 parts
The above-described components are sufficiently mixed and stirred in a stainless steel flask using ULTRA TURRAX (manufactured by IKA). Next, the flask is heated to 48° C. in a heating oil bath under stirring. After the flask is kept at 48° C. for 80 minutes, 70 parts of the resin particle dispersion 1 is added thereto.
Next, the pH in the system is adjusted to 6.0 using a sodium hydroxide aqueous solution having a concentration 0.5 mol/L, the stainless steel flask is sealed, and a stirring shaft is sealed with a magnetic force. The flask is heated to 97° C. under stirring and is kept at 97° C. for 3 hours. After the completion of the reaction, the flask is cooled at a temperature decrease rate of 1° C./min, is filtered, is washed with ion exchange water, and undergoes solid-liquid separation by Nutsche suction filtration. The solid is redispersed in 3 L of ion exchange water at 40° C., is stirred, and is washed at 300 rpm for 15 minutes.
This washing operation is repeated 5 times. In a case where the pH of the filtrate is 6.54 and the electrical conductance is 6.5 μS/cm, solid-liquid separation is performed by Nutsche suction filtration with No. 5A filter paper. Next, the solid is dried in a vacuum for 12 hours. As a result, toner particles K are obtained.
The volume average particle diameter of the toner particles K is 6.2 μm which is measured using COULTER MULTISIZER II (manufactured by Beckman Coulter Co., Ltd.) and an aperture having an aperture size of 50 μm, and the volume average particle diameter distribution index GSDv thereof is 1.20.
The shape factor SF1 of the particles is 135 in a case where the shape thereof is observed using an image analyzer LUZEX (manufactured by Nireco Corporation).
In addition, the glass transition temperature of the toner particles K is 52° C.
Further, silica (SiO2) particles having an average primary particle diameter of 40 nm, which are surface-treated with a hydrophobizing agent of hexamethyldisilazane (HMDS), and metatitanic acid compound particles having an average primary particle diameter of 20 nm, which are a reaction product of metatitanic acid and isobutyl trimethoxy silane, are added to the toner particles K such that a coverage ratio of the surfaces of the toner particles K is 40%. The mixture is mixed using a Henschel mixer. As a result, a toner 1K as a black toner is prepared.
Preparation of Toner 1Y (Yellow Toner), Toner 1M (Magenta Toner), and Toner 1C (Cyan Toner)
A yellow colorant particle dispersion Y, a magenta colorant particle dispersion M, and a cyan colorant particle dispersion C are obtained using the same preparation method as that of the colorant particle dispersion K, except that a yellow pigment (PY180; manufactured by Clariant Japan K.K.), a magenta pigment (PR122; manufactured by DIC Corporation), and a cyan pigment (copper phthalocyanine, C.I. Pigment Blue 15:3; manufactured by Dainichiseika Colr&Chemicals Mfg. Co., Ltd.) are used instead of carbon black, respectively.
Yellow toner particles Y, magenta toner particles M, and cyan toner particles C are prepared using the same preparation method as that of the toner particles K, except that the yellow colorant particle dispersion Y, the magenta colorant particle dispersion M, and the cyan colorant particle dispersion C are used instead of the black colorant particle dispersion K, respectively.
A toner 1Y as a yellow toner, a toner 1M as a magenta toner, and a toner 1C as a cyan toner are obtained using the same method as that of the toner 1K as a black toner, except that the toner particles Y, the toner particles M, and the toner particles C are used instead of the toner particles K.
Titanium oxide particles (1) (trade name: CR-60-2, manufactured by Ishihara Sangyo Kaisha Ltd.): 210 parts
Nonionic surfactant (trade name: NONIPOL 400, manufactured by Sanyo Chemical Industries, Ltd.): 10 parts
Ion exchange water: 480 parts
The above-described materials are mixed with each other, are stirred using a homogenizer (ULTRA TURRAX T50, manufactured by IKA) for 30 minutes, and are dispersed using a high pressure impact dispersing machine (ALTIMIZER HJP30006, manufactured by Sugino Machine Ltd.) for 1 hour. Further, after keeping the dispersion to remove the supernatant, a colorant particle dispersion W (solid content concentration: 30%) in which titanium oxide particles having a number average particle diameter of 300 nm are dispersed is prepared.
White toner particles W are prepared using the same preparation method as that of the toner particles K, except that the white colorant particle dispersion W is used instead of the black colorant particle dispersion K.
A toner 2W as a white toner is obtained using the same method as that of the toner 1K as the black toner, except that the toner particles W are used instead of the toner particles K.
Transparent toner particles T are prepared using the same preparation method as that of the toner particles K, except that the black colorant particle dispersion K is not used.
A toner 2T as a transparent toner is obtained using the same method as that of the toner 1K as the black toner, except that the toner particles T are used instead of the toner particles K.
The configurations of the obtained toners, and values of the dielectric loss tangent measured using the above-described methods are shown in Table 2.
100 parts of the carrier shown in Table 3 and 10 parts of the toner shown in Table 3 are stirred using a V-blender at 40 rpm for 20 minutes and are sieved through a sieve having a pore size of 125 μm. As a result, respective developers are obtained.
Table 3 collectively shows the volume resistivities and the volume average particle diameters of the carriers.
Examples B1 to B6, Comparative Examples B1 and B2, Examples W1 to W6, Comparative Examples W1 and W2, Examples T1 to T6, and Comparative Examples T1 and T2
In the image forming apparatus (Model No.: a modified machine of DocuCentre Color 400, manufactured by Fuji Xerox Co., Ltd.) shown in
The image forming apparatus shown in
Specifically, images are printed on A4-size plain paper (C2 paper, manufactured by Fuji Xerox Co., Ltd.) in the following procedure in a low-temperature and low-humidity environment (temperature: 10° C., humidity: 10% RH).
First, on Day 1, 10000 images having a rectangular patch (5.2 cm×1.2 cm) with an image density of 1% corresponding to 5 colors are continuously printed.
Next, in an initial operation of Day 2, an image of The Imaging Society of Japan Test Chart No. 5 is printed, and then 10000 images having a rectangular patch (5.2 cm×1.2 cm) with an image density 1% corresponding to 5 colors are continuously printed as on Day 1.
The image printing procedure of Day 2 is repeated every day. The number of images having a rectangular patch with an image density 1% corresponding to 5 colors printed until day 10 is 100000.
In an initial operation of the next day, a halftone patch (5.2 cm×6.0 cm) with an image density of 5% is printed on color paper (pink; manufactured by Fuji Xerox Co., Ltd.) using only the developing device 20B. Next, a solid patch (5.2 cm×6.0 cm) is printed on color paper (pink) using only the developing device 20B.
The evaluation is performed using the obtained halftone patch image and the solid patch image. The results are shown in Tables 4 to 6 below.
The volume resistivity ratio of the carriers (the volume resistivity of the second carrier/the volume resistivity of the first carrier) and the volume average particle diameter ratio of the carriers (the volume average particle diameter of the second carrier/the volume average particle diameter of the first carrier) are collectively shown in Tables 4 to 6.
The formation of a white line on the obtained halftone patch image (whether or not there is a portion where a local decrease in density occurs due to removal of the toner) is evaluated by observation using a 10 times magnifying glass.
In the case of the halftone patch image formed using the transparent developer, whether or not there is a portion where a local decrease in brilliance occurs on the halftone image is observed using the 10 times magnifying glass by tilting the paper from the horizontal direction or by changing a viewing angle, thereby evaluating the formation of a white line.
A: the formation of a white line is not observed on the image
B: the portion where a local decrease in density slightly occurs due to removal of the toner is observed, but there are no problems in image quality
C: the formation of a white line is slightly observed on the image
D: the formation of a white line is clearly observed on the image
The density unevenness on the obtained solid patch image is evaluated as described below.
Unevenness in brilliance or unevenness in covering properties is observed by tilting the paper from the horizontal direction or by changing a viewing angle, thereby evaluating unevenness in the image density of the solid patch image.
A: unevenness in image density is not observed, and there are no problems in image quality
B: unevenness in image density is slightly observed, but there are no problems in image quality
C: unevenness in image density is slightly observed
D: unevenness in image density is clearly observed
It is found from the results that, in Examples, formation of a white line which may occur on an image formed after continuous formation of low-density images is suppressed as compared to Comparative Examples.
The foregoing description of the exemplary embodiments of the present invention has been provided for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise forms disclosed. Obviously, many modifications and variations will be apparent to practitioners skilled in the art. The embodiments were chosen and described in order to best explain the principles of the invention and its practical applications, thereby enabling others skilled in the art to understand the invention for various embodiments and with the various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the following claims and their equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2017-185978 | Sep 2017 | JP | national |
This is a divisional application of and claims the priority benefit of U.S. application Ser. No. 15/956,756, filed on Apr. 19, 2018, now pending, and which is based on and claims priority under 35 USC 119 from Japanese Patent Application No. 2017-185978 filed Sep. 27, 2017. Each of the above applications is hereby expressly incorporated by reference, in their entirety, into the present application.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15956756 | Apr 2018 | US |
| Child | 16296174 | US |
