Patent Grant
10642173
This application is based on and claims priority under 35 USC 119 from Japanese Patent Application No. 2018-239226 filed Dec. 21, 2018.
The present disclosure relates to an electrophotographic photoreceptor, a process cartridge, and an image forming apparatus.
Japanese Unexamined Patent Application Publication No. 2011-095665 discloses an electrophotographic photoreceptor including a conductive support, and an intermediate layer and a photosensitive layer disposed on the conductive support in that order, in which the intermediate layer contains a polyolefin and a benzimidazole-based compound.
Japanese Patent No. 3958154 discloses an electrophotographic photoreceptor including a support, and an intermediate layer and a photosensitive layer disposed on the support in that order, in which the intermediate layer contains an electron transporting substance selected from a naphthalene amidine imide compound, a perylene amidine imide compound, and an imide resin.
Japanese patent No. 3958155 discloses an electrophotographic photoreceptor that includes a support, and an intermediate layer and a photosensitive layer disposed on the support in that order, in which the intermediate layer contains an electron transporting substance selected from a naphthalene amidine imide compound and a perylene amidine imide compound.
Japanese Unexamined Patent Application Publication No. 2015-026067 discloses a benzimidazole compound as an electron transporting substance used in an undercoat layer of an electrophotographic photoreceptor.
Japanese Unexamined Patent Application Publication No. 2014-186296 discloses an electrophotographic photoreceptor that includes a support, an undercoat layer, and a photosensitive layer, in which the undercoat layer contains metal oxide particles surface-treated with a silane coupling agent, a binder resin, and an organic acid salt of a metal selected from bismuth, zinc, cobalt, iron, nickel, and copper.
In general, polycyclic electron transporting materials such as those described in the related art documents are used as the material for the undercoat layer for their high electron transporting property; however, the undercoat layer also desirably has a high charge-retaining property. It is considered that holes, which are a minority carrier in the electron transporting material, contribute to the charge-retaining property. Aspects of non-limiting embodiments of the present disclosure relate to an electrophotographic photoreceptor having an excellent charge-retaining property, in which when a perinone compound is contained as the electron transporting material in the undercoat layer, a specific amine compound is contained to control the hole transport.
Aspects of certain non-limiting embodiments of the present disclosure overcome the above disadvantages and/or other disadvantages not described above. However, aspects of the non-limiting embodiments are not required to overcome the disadvantages described above, and aspects of the non-limiting embodiments of the present disclosure may not overcome any of the disadvantages described above.
According to an aspect of the present disclosure, there is provided an electrophotographic photoreceptor that includes a conductive substrate, an undercoat layer on the conductive substrate, and a photosensitive layer on the undercoat layer. The undercoat layer contains at least one perinone compound selected from the group consisting of a compound represented by general formula (1) below and a compound represented by general formula (2) below, an amine compound (A) having an ionization potential of 5.4 eV or more and 5.9 eV or less, and a binder resin, general formula (1)
where: in general formula (1), R11, R12, R13, R14, R15, R16, R17, and R18 each independently represent a hydrogen atom, an alkyl group, an alkoxy group, an aralkyl group, an aryl group, an aryloxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonylalkyl group, an aryloxycarbonylalkyl group, or a halogen atom; R11 and R12 may be bonded to each other to form a ring, so may R12 and R13, and so may R13 and R14; and R15 and R16 may be bonded to each other to form a ring, so may R16 and R17, and so may R17 and R18, and in general formula (2), R21, R22, R23, R24, R25, R26, R27, and R28 each independently represent a hydrogen atom, an alkyl group, an alkoxy group, an aralkyl group, an aryl group, an aryloxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonylalkyl group, an aryloxycarbonylalkyl group, or a halogen atom; R21 and R22 may be bonded to each other to form a ring, so may R22 and R23, and so may R23 and R24; and R25 and R26 may be bonded to each other to form a ring, so may R26 and R27, and so may R27 and R28.
Exemplary embodiments of the present disclosure will be described in detail based on the following figures, wherein:
The exemplary embodiments of the present disclosure will now be described. These description and examples illustrate exemplary embodiments and do not limit the scope of the exemplary embodiments.
In the present disclosure, a numerical range indicated by using “to” is an inclusive range from the minimum value preceding “to” to the maximum value following “to”.
When numerical ranges are described stepwise in the present disclosure, the upper limit or the lower limit of one numerical range may be substituted with an upper limit or a lower limit of a different numerical range also described stepwise. In the numerical ranges described in the present disclosure, the upper limit or the lower limit of one numerical range may be substituted with a value indicated in Examples.
In the present disclosure, the term “step” not only refers to an independent step but also any instance that achieves the desired purpose of that step although such a step is not clearly distinguishable from other steps.
In the present disclosure, each of the components may contain multiple corresponding substances. In the present disclosure, when the amount of a component in a composition is referred and when there are two or more types of substances that correspond to that component in the composition, the amount is the total amount of the two or more types of the substances in the composition unless otherwise noted.
In the present disclosure, the term “main component” refers to a major component. The main component is, for example, a component that accounts for 30 mass % or more of the total mass of a mixture containing multiple components.
In the present disclosure, the “electrophotographic photoreceptor” may be simply referred to as the “photoreceptor”.
Electrophotographic Photoreceptor
A photoreceptor of the exemplary embodiment includes a conductive substrate, an undercoat layer on the conductive substrate, and a photosensitive layer on the undercoat layer.
The photoreceptor of this exemplary embodiment may be of a function-separated type in which the charge generating layer 2 and the charge transporting layer 3 are separately provided as in the photoreceptor 7A illustrated in
The undercoat layer of the photoreceptor of this exemplary embodiment contains at least one perinone compound selected from the group consisting of a compound represented by general formula (1) and a compound represented by general formula (2), an amine compound (A) having an ionization potential of 5.4 eV or more and 5.9 eV or less, and a binder resin.
In the present disclosure, the compound represented by general formula (1) may also be referred to as a perinone compound (1), and the compound represented by general formula (2) may also be referred to as a perinone compound (2).
Since the undercoat layer of the photoreceptor of the exemplary embodiment contains at least one of the perinone compound (1) and the perinone compound (2), and the amine compound (A), the charge-retaining property is excellent. The reason behind this is presumably the following mechanism. In the description below, the perinone compound (1) and the perinone compound (2) are each simply referred to as a perinone compound.
Compared to a photoreceptor including an undercoat layer containing an imide compound (A), an imide compound (B), or an imide compound (C) described below as a main electron transporting material, the photoreceptor including an undercoat layer containing a perinone compound as a main electron transporting material has superior sensitivity. Compared to a photoreceptor including an undercoat layer containing an n-type inorganic fine particles, such as zinc oxide, as a main electron transporting material, the electrical leak resistance is superior. However, when a perinone compound is a main electron transporting material of the undercoat layer, the charge-retaining property is not sufficient. Although the mechanism thereof is not exactly clear, possibly, movement of the minor hole carrier in the perinone compound contained in the undercoat layer causes charges to diffuse and move toward the charge generating material (for example, a phthalocyanine pigment) in the photosensitive layer, and ultimately, the potential of the photoreceptor surface is attenuated.
It has been found that when an amine compound (A) is contained in the undercoat layer together with a perinone compound, the charge-retaining property is improved. A possible mechanism thereof is that the amine compound (A) traps the hole carrier in the perinone compound and thereby suppresses charge migration between the perinone compound and the charge generating material in the photosensitive layer. As a result, diffusion and movement of charges from the undercoat layer to the photosensitive layer are suppressed, and attenuation of the potential of the photoreceptor surface is suppressed.
In the exemplary embodiment, the ionization potential of the amine compound (A) is 5.4 eV or more and 5.9 eV or less and is close to the ionization potential of the perinone compound. Thus, the amine compound (A) serves as an electron donor for the holes in the perinone compound, and possibly the migration of the holes toward the charge generating layer is suppressed.
In the exemplary embodiment, the ionization potential of a chemical substance is measured by using atmospheric photoelectron spectroscope AC-2 (RIKEN KEIKI Co., Ltd.) by applying ultraviolet light to a chemical substance under atmospheric conditions and determining the energy at which photoelectrons are emitted due to the photoelectric effect.
In the description below, the respective layers of the photoreceptor of this exemplary embodiment are described in detail.
Undercoat Layer
The undercoat layer contains at least one selected from the group consisting of a perinone compound (1) and a perinone compound (2), an amine compound (A), and a binder resin. The undercoat layer may further contain inorganic particles and various other additives.
Perinone compound (1) and perinone compound (2) The undercoat layer contains at least one of a perinone compound (1) and a perinone compound (2). The perinone compound (1) is a compound represented by general formula (1) below. The perinone compound (2) is a compound represented by general formula (2) below.
In general formula (1), R11, R12, R13, R14, R15, R16, R17, and R18 each independently represent a hydrogen atom, an alkyl group, an alkoxy group, an aralkyl group, an aryl group, an aryloxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonylalkyl group, an aryloxycarbonylalkyl group, or a halogen atom. Ru11 and R12 may be bonded to each other to form a ring, so may R12 and R13, and so may R13 and R14. R15 and R16 may be bonded to each other to form a ring, so may R16 and R17, and so may R17 and R18.
In general formula (2), R21, R22, R23, R24, R25, R26, R27, and R28 each independently represent a hydrogen atom, an alkyl group, an alkoxy group, an aralkyl group, an aryl group, an aryloxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonylalkyl group, an aryloxycarbonylalkyl group, or a halogen atom. R21 and R22 may be bonded to each other to form a ring, so may R22 and R23, and so may R23 and R24. R25 and R26 may be bonded to each other to form a ring, so may R26 and R27, and so may R27 and R28.
Examples of the alkyl groups represented by R11 to R18 in general formula (1) include substituted or unsubstituted alkyl groups.
Examples of the unsubstituted alkyl groups represented by R11 to R18 in general formula (1) include linear alkyl groups with 1 or more and 20 or less carbon atoms (preferably 1 or more and 10 or less carbon atoms and more preferably 1 or more and 6 or less carbon atoms), branched alkyl groups with 3 or more and 20 or less carbon atoms (preferably 3 or more and 10 or less carbon atoms), and cyclic alkyl groups with 3 or more and 20 or less carbon atoms (preferably 3 or more and 10 or less carbon atoms).
Examples of the linear alkyl groups with 1 or more and 20 or less carbon atoms include a methyl group, an ethyl group, an n-propyl group, an n-butyl group, an n-pentyl group, an n-hexyl group, an n-heptyl group, an n-octyl group, an n-nonyl group, an n-decyl group, an n-undecyl group, an n-dodecyl group, a tridecyl group, an n-tetradecyl group, an n-pentadecyl group, an n-heptadecyl group, an n-octadecyl group, an n-nonadecyl group, and an n-icosyl group.
Examples of the branched alkyl groups with 3 or more and 20 or less carbon atoms include an isopropyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, an isohexyl group, a sec-hexyl group, a tert-hexyl group, an isoheptyl group, a sec-heptyl group, a tert-heptyl group, an isooctyl group, a sec-octyl group, a tert-octyl group, an isononyl group, a sec-nonyl group, a tert-nonyl group, an isodecyl group, a sec-decyl group, a tert-decyl group, an isododecyl group, a sec-dodecyl group, a tert-dodecyl group, a tert-tetradecyl group, and a tert-pentadecyl group.
Examples of the cyclic alkyl groups with 3 or more and 20 or less carbon atoms include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a cyclononyl group, a cyclodecyl group, and polycyclic (for example, bicyclic, tricyclic, and spirocyclic) alkyl groups in which these monocyclic alkyl groups are bonded.
Among these, linear alky groups such as a methyl group and an ethyl group may be used as the unsubstituted alkyl groups.
Examples of the substituent in the alkyl group include an alkoxy group, a hydroxy group, a carboxy group, a nitro group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the alkoxy group that substitutes the hydrogen atom in the alkyl group include the same groups as those unsubstituted alkoxy groups represented by R11 to R18 in general formula (1).
Examples of the alkoxy groups represented by R11 to R18 in general formula (1) include substituted or unsubstituted alkoxy groups.
Examples of the unsubstituted alkoxy groups represented by R11 to R18 in general formula (1) include linear, branched, and cyclic alkoxy groups with 1 or more and 10 or less (preferably 1 or more and 6 or less and more preferably 1 or more and 4 or less) carbon atoms.
Specific examples of the linear alkoxy group include a methoxy group, an ethoxy group, an n-propoxy group, an n-butoxy group, an n-pentyloxy group, an n-hexyloxy group, an n-heptyloxy group, an n-octyloxy group, an n-nonyloxy group, and an n-decyloxy group.
Specific examples of the branched alkoxy group include an isopropoxy group, an isobutoxy group, a sec-butoxy group, a tert-butoxy group, an isopentyloxy group, a neopentyloxy group, a tert-pentyloxy group, an isohexyloxy group, a sec-hexyloxy group, a tert-hexyloxy group, an isoheptyloxy group, a sec-heptyloxy group, a tert-heptyloxy group, an isooctyloxy group, a sec-octyloxy group, a tert-octyloxy group, an isononyloxy group, a sec-nonyloxy group, a tert-nonyloxy group, an isodecyloxy group, a sec-decyloxy group, and a tert-decyloxy group.
Specific examples of the cyclic alkoxy group include a cyclopropoxy group, a cyclobutoxy group, a cyclopentyloxy group, a cyclohexyloxy group, a cycloheptyloxy group, a cyclooctyloxy group, a cyclononyloxy group, and a cyclodecyloxy group.
Among these, a linear alkoxy group may be used as the unsubstituted alkoxy group.
Examples of the substituent in the alkoxy group include an aryl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a hydroxyl group, a carboxy group, a nitro group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the aryl group that substitutes the hydrogen atom in the alkoxy group include the same groups as those unsubstituted aryl groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonyl group that substitutes the hydrogen atom in the alkoxy group include the same groups as those unsubstituted alkoxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonyl group that substitutes the hydrogen atom in the alkoxy group include the same groups as those unsubstituted aryloxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aralkyl groups represented by R11 to R18 in general formula (1) include substituted or unsubstituted aralkyl groups.
The unsubstituted aralkyl group represented by R11 to R18 in general formula (1) are preferably aralkyl groups with 7 or more and 30 or less carbon atoms, more preferably aralkyl groups with 7 or more and 16 or less carbon atoms, and yet more preferably aralkyl groups with 7 or more and 12 or less carbon atoms.
Examples of the unsubstituted aralkyl group with 7 or more and 30 or less carbon atoms include a benzyl group, a phenylethyl group, a phenylpropyl group, a 4-phenylbutyl group, a phenylpentyl group, a phenylhexyl group, a phenylheptyl group, a phenyloctyl group, a phenylnonyl group, a naphthylmethyl group, a naphthylethyl group, an anthracylmethyl group, and a phenyl-cyclopentylmethyl group.
Examples of the substituent in the aralkyl group include an alkoxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the alkoxy group that substitutes the hydrogen atom in the aralkyl group include the same groups as those unsubstituted alkoxy groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonyl group that substitutes the hydrogen atom in the aralkyl group include the same groups as those unsubstituted alkoxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonyl group that substitutes the hydrogen atom in the aralkyl group include the same groups as those unsubstituted aryloxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aryl groups represented by R11 to R18 in general formula (1) include substituted or unsubstituted aryl groups.
The unsubstituted aryl groups represented by R11 to R18 in general formula (1) are preferably aryl groups with 6 or more and 30 or less carbon atoms, more preferably aryl groups with 6 or more and 14 or less carbon atoms, and yet more preferably aryl groups with 6 or more and 10 or less carbon atoms.
Examples of the aryl groups with 6 or more and 30 or less carbon atoms include a phenyl group, a biphenyl group, a 1-naphthyl group, a 2-naphthyl group, a 9-anthryl group, a 9-phenanthryl group, a 1-pyrenyl group, a 5-naphthacenyl group, a 1-indenyl group, a 2-azulenyl group, a 9-fluorenyl group, a biphenylenyl group, an indacenyl group, a fluoranthenyl group, an acenaphthylenyl group, an aceantrylenyl group, a phenalenyl group, a fluorenyl group, an anthryl group, a bianthracenyl group, a teranthracenyl group, a quarteranthracenyl group, an anthraquinolyl group, a phenanthryl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a preadenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a pentacenyl group, a tetraphenylenyl group, a hexaphenyl group, a hexacenyl group, a rubicenyl group, and a coronenyl group. Among these, a phenyl group may be used.
Examples of the substituent in the aryl group include an alkyl group, an alkoxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the alkyl group that substitutes the hydrogen atom in the aryl group include the same groups as those unsubstituted alkyl groups represented by R11 to R18 in general formula (1).
Examples of the alkoxy group that substitutes the hydrogen atom in the aryl group include the same groups as those unsubstituted alkoxy groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonyl group that substitutes the hydrogen atom in the aryl group include the same groups as those unsubstituted alkoxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonyl group that substitutes the hydrogen atom in the aryl group include the same groups as those unsubstituted aryloxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxy groups (—O—Ar where Ar represents an aryl group) represented by R11 to R18 in general formula (1) include substituted or unsubstituted aryloxy groups.
The unsubstituted aryloxy groups represented by R11 to R18 in general formula (1) are preferably aryloxy groups with 6 or more and 30 or less carbon atoms, more preferably aryloxy groups with 6 or more and 14 or less carbon atoms, and yet more preferably aryloxy groups with 6 or more and 10 or less carbon atoms.
Examples of the aryloxy groups with 6 or more and 30 or less carbon atoms include a phenyloxy group (phenoxy group), a biphenyloxy group, a 1-naphthyloxy group, a 2-naphthyloxy group, a 9-anthryloxy group, a 9-phenanthryloxy group, a 1-pyrenyloxy group, a 5-naphthacenyloxy group, a 1-indenyloxy group, a 2-azulenyloxy group, a 9-fluorenyloxy group, a biphenylenyloxy group, an indacenyloxy group, a fluoranthenyloxy group, an acenaphthylenyloxy group, an aceantrylenyloxy group, a phenalenyloxy group, a fluorenyloxy group, an anthryloxy group, a bianthracenyloxy group, a teranthracenyloxy group, a quarteranthracenyloxy group, an anthraquinolyloxy group, a phenanthryloxy group, a triphenylenyloxy group, a pyrenyloxy group, a chrysenyloxy group, a naphthacenyloxy group, a preadenyloxy group, a picenyloxy group, a perylenyloxy group, a pentaphenyloxy group, a pentacenyloxy group, a tetraphenylenyloxy group, a hexaphenyloxy group, a hexacenyloxy group, a rubicenyloxy group, and a coronenyloxy group. Among these, a phenyloxy group (phenoxy group) may be used.
Examples of the substituent in the aryloxy group include an alkyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the alkyl group that substitutes the hydrogen atom in the aryloxy group include the same groups as those unsubstituted alkyl groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonyl group that substitutes the hydrogen atom in the aryloxy group include the same groups as those unsubstituted alkoxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonyl group that substitutes the hydrogen atom in the aryloxy group include the same groups as those unsubstituted aryloxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonyl groups (—CO—OR where R represents an alkyl group) represented by R1 to R18 in general formula (1) include substituted or unsubstituted alkoxycarbonyl groups.
The number of carbon atoms in the alkyl chain in the unsubstituted alkoxycarbonyl groups represented by R11 to R18 in general formula (1) is preferably 1 or more and 20 or less, more preferably 1 or more and 15 or less, and yet more preferably 1 or more and 10 or less.
Examples of the alkoxycarbonyl group having an alkyl chain with 1 or more and 20 or less carbon atoms include a methoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, an isopropoxycarbonyl group, an n-butoxycarbonyl group, a sec-butoxybutylcarbonyl group, a tert-butoxycarbonyl group, a pentaoxycarbonyl group, a hexaoxycarbonyl group, a heptaoxycarbonyl group, an octaoxycarbonyl group, a nonaoxycarbonyl group, a decaoxycarbonyl group, a dodecaoxycarbonyl group, a tridecaoxycarbonyl group, a tetradecaoxycarbonyl group, a pentadecaoxycarbonyl group, a hexadecaoxycarbonyl group, a heptadecaoxycarbonyl group, an octadecaoxycarbonyl group, a nonadecaoxycarbonyl group, and an icosaoxycarbonyl group.
Examples of the substituent in the alkoxycarbonyl group include an aryl group, a hydroxy group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the aryl group that substitutes the hydrogen atom in the alkoxycarbonyl group include the same groups as those unsubstituted aryl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonyl groups (—CO—OAr where Ar represents an aryl group) represented by R1 to R18 in general formula (1) include substituted or unsubstituted aryloxycarbonyl groups.
The number of carbon atoms in the aryl group in the unsubstituted aryloxycarbonyl groups represented by R11 to R18 in general formula (1) is preferably 6 or more and 30 or less, more preferably 6 or more and 14 or less, and yet more preferably 6 or more and 10 or less.
Examples of the aryloxycarbonyl group having an aryl group with 6 or more and 30 or less carbon atoms include a phenoxycarbonyl group, a biphenyloxycarbonyl group, a 1-naphthyloxycarbonyl group, a 2-naphthyloxycarbonyl group, a 9-anthryloxycarbonyl group, a 9-phenanthryloxycarbonyl group, a 1-pyrenyloxycarbonyl group, a 5-naphthacenyloxycarbonyl group, a 1-indenyloxycarbonyl group, a 2-azulenyloxycarbonyl group, a 9-fluorenyloxycarbonyl group, a biphenylenyloxycarbonyl group, an indacenyloxycarbonyl group, a fluoranthenyloxycarbonyl group, an acenaphthylenyloxycarbonyl group, an aceantrylenyloxycarbonyl group, a phenalenyloxycarbonyl group, a fluorenyloxycarbonyl group, an anthryloxycarbonyl group, a bianthracenyloxycarbonyl group, a teranthracenyloxycarbonyl group, a quarteranthracenyloxycarbonyl group, an anthraquinolyloxycarbonyl group, a phenanthryloxycarbonyl group, a triphenylenyloxycarbonyl group, a pyrenyloxycarbonyl group, a chrysenyloxycarbonyl group, a naphthacenyloxycarbonyl group, a preadenyloxycarbonyl group, a picenyloxycarbonyl group, a perylenyloxycarbonyl group, a pentaphenyloxycarbonyl group, a pentacenyloxycarbonyl group, a tetraphenylenyloxycarbonyl group, a hexaphenyloxycarbonyl group, a hexacenyloxycarbonyl group, a rubicenyloxycarbonyl group, and a coronenyloxycarbonyl group. Among these, a phenoxycarbonyl group may be used.
Examples of the substituent in the aryloxycarbonyl group include an alkyl group, a hydroxy group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the alkyl group that substitutes the hydrogen atom in the aryloxycarbonyl group include the same groups as those unsubstituted alkyl groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonylalkyl groups (—(CnH2n)—CO—OR where R represents an alkyl group and n represents an integer of 1 or more) represented by R11 to R18 in general formula (1) include substituted or unsubstituted alkoxycarbonylalkyl groups.
Examples of the alkoxycarbonyl group (—CO—OR) in the unsubstituted alkoxycarbonylalkyl groups represented by R11 to R18 in general formula (1) include the same groups as those alkoxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the alkylene chain (—CnH2n—) in the unsubstituted alkoxycarbonylalkyl groups represented by R11 to R18 in general formula (1) include linear alkylene chains with 1 or more and 20 or less carbon atoms (preferably 1 or more and 10 or less carbon atoms and more preferably 1 or more and 6 or less carbon atoms), branched alkylene chains with 3 or more and 20 or less carbon atoms (preferably 3 or more and 10 or less carbon atoms), and cyclic alkylene chains with 3 or more and 20 or less carbon atoms (preferably 3 or more and 10 or less carbon atoms).
Examples of the linear alkylene chain with 1 or more and 20 or less carbon atoms include a methylene group, an ethylene group, an n-propylene group, an n-butylene group, an n-pentylene group, an n-hexylene group, an n-heptylene group, an n-octylene group, an n-nonylene group, an n-decylene group, an n-undecylene group, an n-dodecylene group, a tridecylene group, an n-tetradecylene group, an n-pentadecylene group, an n-heptadecylene group, an n-octadecylene group, an n-nonadecylene group, and an n-icosylene group.
Examples of the branched alkylene chain with 3 or more and 20 or less carbon atoms include an isopropylene group, an isobutylene group, a sec-butylene group, a tert-butylene group, an isopentylene group, a neopentylene group, a tert-pentylene group, an isohexylene group, a sec-hexylene group, a tert-hexylene group, an isoheptylene group, a sec-heptylene group, a tert-heptylene group, an isooctylene group, a sec-octylene group, a tert-octylene group, an isononylene group, a sec-nonylene group, a tert-nonylene group, an isodecylene group, a sec-decylene group, a tert-decylene group, an isododecylene group, a sec-dodecylene group, a tert-dodecylene group, a tert-tetradecylene group, and a tert-pentadecylene group.
Examples of the cyclic alkylene chain with 3 or more and 20 or less carbon atoms include a cyclopropylene group, a cyclobutylene group, a cyclopentylene group, a cyclohexylene group, a cycloheptylene group, a cyclooctylene group, a cyclononylene group, and a cyclodecylene group.
Examples of the substituent in the alkoxycarbonylalkyl group include an aryl group, a hydroxy group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the aryl group that substitutes the hydrogen atom in the alkoxycarbonylalkyl group include the same groups as those unsubstituted aryl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonylalkyl groups (—(CnH2n)—CO—OAr where Ar represents an aryl group and n represents an integer of 1 or more) represented by R11 to R18 in general formula (1) include substituted or unsubstituted aryloxycarbonylalkyl groups.
Examples of the aryloxycarbonyl group (—CO—OAr where Ar represents an aryl group) in the unsubstituted aryloxycarbonylalkyl groups represented by R11 to R18 in general formula (1) include the same groups as those aryloxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of alkylene chain (—CnH2n—) in the unsubstituted aryloxycarbonylalkyl groups represented by R11 to R18 in general formula (1) include the same groups as those alkylene chains in the alkoxycarbonylalkyl groups represented by R11 to R18 in general formula (1).
Examples of the substituent in the aryloxycarbonylalkyl group include an alkyl group, a hydroxy group, and a halogen atom (fluorine atom, bromine atom, iodine atom, etc.).
Examples of the alkyl group that substitutes the hydrogen atom in the aryloxycarbonylalkyl group include the same groups as those unsubstituted alkyl groups represented by R11 to R18 in general formula (1).
Examples of the halogen atoms represented by R11 to R18 in general formula (1) include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
In general formula (1), examples of the ring structure formed as a result of bonding between R1 and R12, R12 and R13, R13 and R14, R15 and R16, R16 and R17, or R17 and R18 include a benzene ring and fused rings with 10 or more and 18 or less carbon atoms (a naphthalene ring, an anthracene ring, a phenanthrene ring, a chrysene ring (benzo[c]phenanthrene ring), a tetracene ring, a tetraphene ring (benzo[α]anthracene ring), a triphenylene ring, etc.). Among these, a benzene ring is preferable as the ring structure to be formed.
Examples of the alkyl groups represented by R21 to R28 in general formula (2) include the same groups as those alkyl groups represented by R11 to R18 in general formula (1).
Examples of the alkoxy groups represented by R21 to R28 in general formula (2) include the same groups as those alkoxy groups represented by R11 to R18 in general formula (1).
Examples of the aralkyl groups represented by R21 to R28 in general formula (2) include the same groups as those aralkyl groups represented by R11 to R18 in general formula (1).
Examples of the aryl groups represented by R21 to R28 in general formula (2) include the same groups as those aryl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxy groups represented by R21 to R28 in general formula (2) include the same groups as those aryloxy groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonyl groups represented by R21 to R28 in general formula (2) include the same groups as those alkoxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonyl groups represented by R21 to R28 in general formula (2) include the same groups as those aryloxycarbonyl groups represented by R11 to R18 in general formula (1).
Examples of the alkoxycarbonylalkyl groups represented by R21 to R28 in general formula (2) include the same groups as those alkoxycarbonylalkyl groups represented by R11 to R18 in general formula (1).
Examples of the aryloxycarbonylalkyl groups represented by R21 to R28 in general formula (2) include the same groups as those aryloxycarbonylalkyl groups represented by R11 to R18 in general formula (1).
Examples of the halogen atoms represented by R21 to R28 in general formula (2) include the same atoms as those halogen atoms represented by R11 to R18 in general formula (1).
In general formula (2), examples of the ring structure formed as a result of bonding between R21 and R22, R22 and R23, R23 and R24, R25 and R26, R26 and R27, or R27 and R28 include a benzene ring and fused rings with 10 or more and 18 or less carbon atoms (a naphthalene ring, an anthracene ring, a phenanthrene ring, a chrysene ring (benzo[c]phenanthrene ring), a tetracene ring, a tetraphene ring (benzo[α]anthracene ring), a triphenylene ring, etc.). Among these, a benzene ring is preferable as the ring structure to be formed.
From the viewpoint of excellent leak resistance, in general formula (1), R11, R12, R13, R14, R15, R16, R17, and R18 may each independently represent a hydrogen atom, an alkyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonylalkyl group, or an aryloxycarbonylalkyl group.
From the viewpoint of excellent leak resistance, in general formula (2), R21, R22, R23, R24, R25, R26, R27, and R28 may each independently represent a hydrogen atom, an alkyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxycarbonylalkyl group, or an aryloxycarbonylalkyl group.
Specific examples of the perinone compound (1) and the perinone compound (2) are described below, but the exemplary embodiment is not limited by these examples.
The perinone compound (1) and the perinone compound (2) are isomeric to each other (in other words, have a cis/trans relationship). According to a typical synthesis method, 2 moles of an orthophenylenediamine compound and 1 mole of naphthalenetetracarboxylic acid compound are heated and fused, as a result of which a mixture of a cis isomer and a trans isomer is obtained. Typically, the mixing ratio is greater for the cis isomer than the trans isomer. The cis isomer and the trans isomer can be isolated from each other by, for example, heating and washing the mixture with an alcohol solution of potassium hydroxide since the cis isomer is soluble and the trans isomer is sparingly soluble in this solution.
The total amount of the perinone compound (1) and the perinone compound (2) relative to the total solid content of the undercoat layer is preferably 30 mass % or more and 90 mass % or less, more preferably 40 mass % or more and 80 mass % or less, and yet more preferably 50 mass % or more and 75 mass % or less from the viewpoint of controlling the volume resistivity of the undercoat layer to be within a desirable range.
Amine Compound (A)
The undercoat layer of this exemplary embodiment includes at least one amine compound (A). The type of the amine compound is not particularly limited and may be primary amine, secondary amine, or tertiary amine.
The amine compound (A) may be, for example, an amine compound known as a urethane-curing catalyst, an amine compound known as a silane coupling agent, an amine compound known as a chelating agent, or an amine compound added to a composition for forming the undercoat layer with an expectation of these functions.
The ionization potential of the amine compound (A) is 5.4 eV or more and 5.9 eV or less and preferably 5.5 eV or more and 5.8 eV or less.
The amine compound having an ionization potential of 5.4 eV or more and 5.9 eV or less is not particularly limited, and the examples include the following.
A compound represented by structural formula (1) below (Ip: 5.41 eV)
A compound represented by structural formula (2) below (Ip: 5.49 eV)
A compound represented by structural formula (3) below (Ip: 5.50 eV)
A compound represented by structural formula (4) below (Ip: 5.56 eV)
A compound represented by structural formula (5) below (Ip: 5.64 eV)
A compound represented by structural formula (6) below (Ip: 5.65 eV)
N-2-(Aminoethyl)-3-aminopropyltrimethoxysilane (Ip: 5.75 eV)
A compound represented by structural formula (7) below (Ip: 5.77 eV)
A compound represented by structural formula (8) below (Ip: 5.78 eV)
1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU, Ip: 5.82 eV)
1,4-Diazabicyclo[2.2.2]octane (Ip: 5.87 eV)
The ionization potentials of these amine compounds can be measured with photoelectron spectroscope AC-2 produced by RIKEN KEIKI Co., Ltd.
These amine compounds may be used alone or in combination.
The amount of the amine compound (A) contained relative to the total solid content of the undercoat layer is preferably 0.01 mmol/g or more and 1 mmol/g or less, more preferably 0.05 mmol/g or more and 0.9 mmol/g or less, and yet more preferably 0.1 mmol/g or more and 0.8 mmol/g or less.
Binder Resin
The type of the binder resin contained in the undercoat layer is not limited. Examples of the binder contained in the undercoat layer include polyurethane, polyvinyl alcohol resins, polyvinyl acetal resins, casein resins, polyamide resins, cellulose resins, gelatin, polyester resins, unsaturated polyester resins, methacrylic resins, acrylic resins, polyvinyl chloride resins, polyvinyl acetate resins, vinyl chloride-vinyl acetate-maleic anhydride resins, silicone resins, silicone-alkyd resins, urea resin, phenolic resins, phenol-formaldehyde resins, melamine resins, alkyd resins, and epoxy resins. The binder resin contained in the undercoat layer may be polyurethane from the viewpoint of further improving the charge-retaining property of the undercoat layer.
Polyurethane
The undercoat layer of the exemplary embodiment may contain polyurethane as a binder resin. When polyurethane is used as the binder resin, the charge-retaining property is excellent compared to when other types of binder resins are used. A possible mechanism therefor is that polyurethane has a large effect (trapping effect) of suppressing injection of inner charges (cark carrier) of the perinone compound (1) or (2) contained in the undercoat layer into the charge generating material, and thus attenuation of the potential on the photoreceptor surface is suppressed.
Polyurethane is typically synthesized by a polyaddition reaction between a polyisocyanate and a polyol.
Examples of the polyisocyanate include diisocyanates such as methylene diisocyanate, ethylene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, 1,4-cyclohexane diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 1,3-xylylene diisocyanate, 1,5-naphthalene diisocyanate, m-phenylene diisocyanate, p-phenylene diisocyanate, 3,3′-dimethyl-4,4′-diphenylmethane diisocyanate, 3,3′-dimethylbiphenylene diisocyanate, 4,4′-biphenylene diisocyanate, dicyclohexylmethane diisocyanate, and methylene bis(4-cyclohexyl isocyanate); isocyanurates obtained by trimerizing these diisocyanates; and blocked isocyanates obtained by blocking the isocyanate groups of the diisocyanates with a blocking agent. Polyisocyanates may be used alone or in combination.
Examples of the polyol include diols such as ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 2,3-butanediol, 2,2-dimethyl-1,3-propanediol, 1,2-pentanediol, 1,4-pentanediol, 1,5-pentanediol, 2,4-pentanediol, 3,3-dimethyl-1,2-butanediol, 2-ethyl-2-methyl-1,3-propanediol, 1,2-hexanediol, 1,5-hexanediol, 1,6-hexanediol, 2,5-hexanediol, 2-methyl-2,4-pentanediol, 2,2-diethyl-1,3-propanediol, 2,4-dimethyl-2,4-pentanediol, 1,7-heptanediol, 2-methyl-2-propyl-1,3-propanediol, 2,5-dimethyl-2,5-hexanediol, 2-ethyl-1,3-hexanediol, 1,2-octanediol, 1,8-octanediol, 2,2,4-trimethyl-1,3-pentanediol, 1,4-cyclohexanedimethanol, hydroquinone, diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, polyethylene glycol, polypropylene glycol, poly(oxytetramethylene)glycol, 4,4′-dihydroxy-diphenyl-2,2-propane, and 4,4′-dihydroxyphenylsulfone.
Examples of the polyol further include polyester polyol, polycarbonate polyol, polycaprolactone polyol, polyether polyol, and polyvinyl butyral.
The polyols may be used alone or in combination.
Examples of the urethane-curing catalyst (in other words, a catalyst of the polyaddition reaction between a polyisocyanate and a polyol) include amine compounds, organic acid metal salts, and organic metal complexes. Examples of the amine compounds include N,N-dimethylcyclohexylamine, N-methyldicyclohexylamine, N,N,N′,N′-tetramethylpropylenediamine, N-ethylmorpholine, N-methylmorpholine, N, N-dimethylethanolamine, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), and salts thereof. Examples of the organic acid metal salts and organic metal complexes include dibutyl tin laurate, stannous octoate, bismuth octylate, bismuth naphthenate, bismuth salicylate, zinc octylate, zinc naphthenate, and zinc salicylate.
The binder resin contained in the undercoat layer preferably contains 80 mass % or more and 100 mass % or less, more preferably 90 mass % or more and 100 mass % or less, and yet more preferably 95 mass % or more and 100 mass % or less of the polyurethane relative to the total amount of the binder resin.
The mass ratio (perinone compounds:polyurethane) of the total amount of the perinone compound (1) and the perinone compound (2) contained in the undercoat layer to the amount of the polyurethane contained in the undercoat layer is preferably from 90:10 to 50:50 and more preferably from 80:20 to 70:30.
Metal Oxide Particles
The undercoat layer preferably contains metal oxide particles from the viewpoint of suppressing occurrence of leaks caused by foreign matter piercing the photoreceptor. Examples of the metal oxide particles include zinc oxide particles, titanium oxide particles, tin oxide particles, and zirconium oxide particles, and zinc oxide particles, titanium oxide particles, or tin oxide particles are preferable.
The volume-average particle diameter of the metal oxide particles is preferably 50 nm or more and 2000 nm or less and more preferably 60 nm or more and 1000 nm or less.
The specific surface area of the metal oxide particles measured by the BET method may be 10 m2/g or more.
The metal oxide particles may be surface-treated. Examples of the surface treatment agent for the metal oxide particles include a silane coupling agent, a titanate-based coupling agent, an aluminum-based coupling agent, and a surfactant. The metal oxide particles may be a mixture of two or more types of metal oxide particles of different metals, metal particles subjected to different surface treatments, or metal oxide particles having different particle diameters.
When the undercoat layer contains metal oxide particles in order to suppress occurrence of leaks caused by foreign matter piercing the photoreceptor, the amount of the metal oxide particles contained relative to the total solid content of the undercoat layer is preferably 1 mass % or more and less than 30 mass % and more preferably 5 mass % or more and 20 mass % or less.
The undercoat layer may contain various additives to improve electrical properties, environmental stability, and image quality.
Examples of the additives include known materials such as electron transporting pigments based on polycyclic condensed materials and azo materials, zirconium chelate compounds, titanium chelate compounds, aluminum chelate compounds, titanium alkoxide compounds, organic titanium compounds, and silane coupling agents. The silane coupling agent is used to surface-treat the metal oxide particles as mentioned above, but may be further added as an additive to the undercoat layer.
Examples of the silane coupling agent used as an additive include vinyltrimethoxysilane, 3-methacryloxypropyl-tris(2-methoxyethoxy)silane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxy silane, 3-glycidoxypropyltrimethoxysilane, vinyltriacetoxysilane, 3-mercaptopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, N-2-(aminoethyl)-3-aminopropyltrimethoxysilane, N-2-(aminoethyl)-3-aminopropylmethyldimethoxysilane, N,N-bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane, and 3-chloropropyltrimethoxysilane.
Examples of the zirconium chelate compounds include zirconium butoxide, zirconium ethyl acetoacetate, zirconium triethanolamine, acetylacetonate zirconium butoxide, ethyl acetoacetate zirconium butoxide, zirconium acetate, zirconium oxalate, zirconium lactate, zirconium phosphonate, zirconium octanoate, zirconium naphthenate, zirconium laurate, zirconium stearate, zirconium isostearate, methacrylate zirconium butoxide, stearate zirconium butoxide, and isostearate zirconium butoxide.
Examples of the titanium chelate compounds include tetraisopropyl titanate, tetra-n-butyl titanate, butyl titanate dimer, tetra(2-ethylhexyl) titanate, titanium acetylacetonate, polytitanium acetylacetonate, titanium octylene glycolate, titanium lactate ammonium salt, titanium lactate, titanium lactate ethyl ester, titanium triethanol aminate, and polyhydroxy titanium stearate.
Examples of the aluminum chelate compounds include aluminum isopropylate, monobutoxyaluminum diisopropylate, aluminum butylate, diethylacetoacetate aluminum diisopropylate, and aluminum tris(ethylacetoacetate).
These additives may be used alone, or two or more compounds may be used as a mixture or a polycondensation product.
The thickness of the undercoat layer is preferably 3 μm or more and more preferably 5 μm or more from the viewpoint of excellent leak resistance. The thickness of the undercoat layer is preferably 50 μm or less, more preferably 40 μm or less, and yet more preferably 30 μm or less from the viewpoint of the excellent charge-retaining property.
The volume resistivity of the undercoat layer may be 1×1010 Ω·cm or more and 1×1012 Ω·cm or less.
The undercoat layer may have a Vickers hardness of 35 or more.
In order to suppress moire images, the surface roughness (ten-point average roughness) of the undercoat layer may be adjusted to be in the range of 1/(4n) (n represents the refractive index of the overlying layer) to ½ of λ representing the laser wavelength used for exposure.
In order to adjust the surface roughness, resin particles and the like may be added to the undercoat layer. Examples of the resin particles include silicone resin particles, and crosslinking polymethyl methacrylate resin particles. The surface of the undercoat layer may be polished to adjust the surface roughness. Examples of the polishing method included buff polishing, sand blasting, wet honing, and grinding.
The undercoat layer may be formed by any known method. For example, a coating film is formed by using an undercoat-layer-forming solution prepared by adding the above-mentioned components to a solvent, dried, and, if needed, heated.
Examples of the solvent used for preparing the undercoat-layer-forming solution include known organic solvents, such as alcohol solvents, aromatic hydrocarbon solvents, halogenated hydrocarbon solvents, ketone solvents, ketone alcohol solvents, ether solvents, and ester solvents.
Specific examples of the solvent include common organic solvents such as methanol, ethanol, n-propanol, iso-propanol, n-butanol, benzyl alcohol, methyl cellosolve, ethyl cellosolve, acetone, methyl ethyl ketone, cyclohexanone, methyl acetate, ethyl acetate, n-butyl acetate, dioxane, tetrahydrofuran, methylene chloride, chloroform, chlorobenzene, and toluene.
Since the perinone compound (1) and the perinone compound (2) are sparingly soluble in organic solvents, they may be dispersed in an organic solvent. Examples of the dispersing method include known methods that use a roll mill, a ball mill, a vibrating ball mill, an attritor, a sand mill, a colloid mill, and a paint shaker. When metal oxide particles are added to the undercoat layer, the metal oxide particles may also be dispersed in an organic solvent by the same dispersing method.
Examples of the method for applying the undercoat-layer-forming solution to the conductive substrate include common methods such as a blade coating method, a wire bar coating method, a spray coating method, a dip coating method, a bead coating method, an air knife coating method, and a curtain coating method.
Conductive Substrate
Examples of the conductive substrate include metal plates, metal drums, and metal belts that contain metals (aluminum, copper, zinc, chromium, nickel, molybdenum, vanadium, indium, gold, platinum, etc.) or alloys (stainless steel etc.). Other examples of the conductive substrate include paper sheets, resin films, and belts coated, vapor-deposited, or laminated with conductive compounds (for example, conductive polymers and indium oxide), metals (for example, aluminum, palladium, and gold), or alloys. Here, “conductive” means having a volume resistivity of less than 1×1013 Ω·cm.
The surface of the conductive substrate may be roughened to a center-line average roughness Ra of 0.04 μm or more and 0.5 μm or less in order to suppress interference fringes that occur when the electrophotographic photoreceptor used in a laser printer is irradiated with a laser beam. When incoherent light is used as a light source, there is no need to roughen the surface to prevent interference fringes, but roughening the surface suppresses generation of defects due to irregularities on the surface of the conductive substrate and thus is desirable for extending the lifetime.
Examples of the surface roughening method include a wet honing method with which an abrasive suspended in water is sprayed onto a conductive support, a centerless grinding with which a conductive substrate is pressed against a rotating grinding stone to perform continuous grinding, and an anodization treatment.
Another example of the surface roughening method does not involve roughening the surface of a conductive substrate but involves dispersing a conductive or semi-conductive powder in a resin and forming a layer of the resin on a surface of a conductive substrate so as to create a rough surface by the particles dispersed in the layer.
The surface roughening treatment by anodization involves forming an oxide film on the surface of a conductive substrate by anodization by using a metal (for example, aluminum) conductive substrate as the anode in an electrolyte solution. Examples of the electrolyte solution include a sulfuric acid solution and an oxalic acid solution. However, a porous anodization film formed by anodization is chemically active as is, is prone to contamination, and has resistivity that significantly varies depending on the environment. Thus, a pore-sealing treatment may be performed on the porous anodization film so as to seal fine pores in the oxide film by volume expansion caused by hydrating reaction in pressurized steam or boiling water (a metal salt such as a nickel salt may be added) so that the oxide is converted into a more stable hydrous oxide.
The thickness of the anodization film may be, for example, 0.3 μm or more and 15 μm or less. When the thickness is within this range, a barrier property against injection tends to be exhibited, and the increase in residual potential caused by repeated use tends to be suppressed.
The conductive substrate may be subjected to a treatment with an acidic treatment solution or a Boehmite treatment.
The treatment with an acidic treatment solution is, for example, conducted as follows. First, an acidic treatment solution containing phosphoric acid, chromic acid, and hydrofluoric acid is prepared. The blend ratios of phosphoric acid, chromic acid, and hydrofluoric acid in the acidic treatment solution may be, for example, in the range of 10 mass % or more and 11 mass % or less for phosphoric acid, in the range of 3 mass % or more and 5 mass % or less for chromic acid, and in the range of 0.5 mass % or more and 2 mass % or less for hydrofluoric acid; and the total concentration of these acids may be in the range of 13.5 mass % or more and 18 mass % or less. The treatment temperature may be, for example, 42° C. or higher and 48° C. or lower. The thickness of the film may be 0.3 μm or more and 15 μm or less.
The Boehmite treatment is conducted by immersing a conductive substrate in pure water at 90° C. or higher and 100° C. or lower for 5 to 60 minutes or by bringing a conductive substrate into contact with pressurized steam at 90° C. or higher and 120° C. or lower for 5 to 60 minutes. The thickness of the film may be 0.1 μm or more and 5 μm or less. The Boehmite-treated body may be further anodized by using an electrolyte solution, such as adipic acid, boric acid, a borate salt, a phosphate salt, a phthalate salt, a maleate salt, a benzoate salt, a tartrate salt, or a citrate salt, that has low film-dissolving power.
Intermediate Layer
Although not illustrated in the drawings, an intermediate layer may be further provided between the undercoat layer and the photosensitive layer.
The intermediate layer is, for example, a layer that contains a resin. Examples of the resin used in the intermediate layer include polymer compounds such as acetal resins (for example, polyvinyl butyral), polyvinyl alcohol resins, polyvinyl acetal resins, casein resins, polyamide resins, cellulose resins, gelatin, polyurethane resins, polyester resins, methacrylic resins, acrylic resins, polyvinyl chloride resins, polyvinyl acetate resins, vinyl chloride-vinyl acetate-maleic anhydride resins, silicone resins, silicone-alkyd resins, phenol-formaldehyde resins, and melamine resins.
The intermediate layer may contain an organic metal compound. Examples of the organic metal compound used in the intermediate layer include organic metal compounds containing metal atoms such as zirconium, titanium, aluminum, manganese, and silicon.
These compounds used in the intermediate layer may be used alone, or two or more compounds may be used as a mixture or a polycondensation product.
In particular, the intermediate layer may be a layer that contains an organic metal compound that contains zirconium atoms or silicon atoms.
The intermediate layer may be formed by any known method. For example, a coating film is formed by using an intermediate-layer-forming solution prepared by adding the above-mentioned components to a solvent, dried, and, if needed, heated.
Examples of the application method for forming the intermediate layer include common methods such as a dip coating method, a lift coating method, a wire bar coating method, a spray coating method, a blade coating method, a knife coating method, and a curtain coating method.
The thickness of the intermediate layer may be set within the range of, for example, 0.1 μm or more and 3 μm or less. The intermediate layer may be used as the undercoat layer.
Function-Separated Type Photosensitive Layer
Charge Generating Layer
The charge generating layer is, for example, a layer that contains a charge generating material and a binder resin. The charge generating layer may be a vapor deposited layer of a charge generating material. The vapor deposited layer of the charge generating material may be used when an incoherent light such as a light emitting diode (LED) or an organic electro-luminescence (EL) image array is used.
Examples of the charge generating material include azo pigments such as bisazo and trisazo pigments; fused-ring aromatic pigments such as dibromoanthanthrone; perylene pigments; pyrrolopyrrole pigments; phthalocyanine pigments; zinc oxide; and trigonal selenium.
Among these, in order to be compatible to the near-infrared laser exposure, a metal phthalocyanine pigment or a metal-free phthalocyanine pigment may be used as the charge generating material. Specific examples thereof include hydroxygallium phthalocyanine, dichlorotin phthalocyanine, and titanyl phthalocyanine.
In order to be compatible to the near ultraviolet laser exposure, the charge generating material may be a fused-ring aromatic pigment such as dibromoanthanthrone, a thioindigo pigment, a porphyrazine compound, zinc oxide, trigonal selenium, a bisazo pigment.
When an incoherent light source, such as an LED or an organic EL image array having an emission center wavelength in the range of 450 nm or more and 780 nm or less, is used, the charge generating material described above may be used; however, from the viewpoint of the resolution, when the photosensitive layer is as thin as 20 μm or less, the electric field intensity in the photosensitive layer is increased, charges injected from the substrate are decreased, and image defects known as black spots tend to occur. This is particularly noticeable when a charge generating material, such as trigonal selenium or a phthalocyanine pigment, that is of a p-conductivity type and easily generates dark current is used.
In contrast, when an n-type semiconductor, such as a fused-ring aromatic pigment, a perylene pigment, or an azo pigment, is used as the charge generating material, dark current rarely occurs and, even when the thickness is small, image defects known as black spots can be suppressed.
Whether n-type or not is determined by a time-of-flight method commonly employed, on the basis of the polarity of the photocurrent flowing therein. A material in which electrons flow more smoothly as carriers than holes is determined to be of an n-type.
The binder resin used in the charge generating layer is selected from a wide range of insulating resins. Alternatively, the binder resin may be selected from organic photoconductive polymers, such as poly-N-vinylcarbazole, polyvinyl anthracene, polyvinyl pyrene, and polysilane.
Examples of the binder resin include, polyvinyl butyral resins, polyarylate resins (polycondensates of bisphenols and aromatic dicarboxylic acids etc.), polycarbonate resins, polyester resins, phenoxy resins, vinyl chloride-vinyl acetate copolymers, polyamide resins, acrylic resins, polyacrylamide resins, polyvinyl pyridine resins, cellulose resins, urethane resins, epoxy resins, casein, polyvinyl alcohol resins, and polyvinyl pyrrolidone resins. Here, “insulating” means having a volume resistivity of 1×1013 Ω·cm or more.
These binder resins are used alone or in combination as a mixture.
The blend ratio of the charge generating material to the binder resin may be in the range of 10:1 to 1:10 on a mass ratio basis.
The charge generating layer may contain other known additives.
The charge generating layer may be formed by any known method. For example, a coating film is formed by using an charge-generating-layer-forming solution prepared by adding the above-mentioned components to a solvent, dried, and, if needed, heated. The charge generating layer may be formed by vapor-depositing a charge generating material. The charge generating layer may be formed by vapor deposition particularly when a fused-ring aromatic pigment or a perylene pigment is used as the charge generating material.
Specific examples of the solvent for preparing the charge-generating-layer-forming solution include methanol, ethanol, n-propanol, n-butanol, benzyl alcohol, methyl cellosolve, ethyl cellosolve, acetone, methyl ethyl ketone, cyclohexanone, methyl acetate, n-butyl acetate, dioxane, tetrahydrofuran, methylene chloride, chloroform, chlorobenzene, and toluene. These solvents are used alone or in combination as a mixture.
The method for dispersing particles (for example, the charge generating material) in the charge-generating-layer-forming solution can use a media disperser such as a ball mill, a vibrating ball mill, an attritor, a sand mill, or a horizontal sand mill, or a media-less disperser such as stirrer, an ultrasonic disperser, a roll mill, or a high-pressure homogenizer. Examples of the high-pressure homogenizer include a collision-type homogenizer in which the dispersion in a high-pressure state is dispersed through liquid-liquid collision or liquid-wall collision, and a penetration-type homogenizer in which the fluid in a high-pressure state is caused to penetrate through fine channels.
In dispersing, it is effective to set the average particle diameter of the charge generating material in the charge-generating-layer-forming solution to 0.5 μm or less, 0.3 μm or less, or 0.15 μm or less.
Examples of the method for applying the charge-generating-layer-forming solution to the undercoat layer (or the intermediate layer) include common methods such as a blade coating method, a wire bar coating method, a spray coating method, a dip coating method, a bead coating method, an air knife coating method, and a curtain coating method.
The thickness of the charge generating layer may be set within the range of, for example, 0.1 μm or more and 5.0 μm or less, or within the range of 0.2 μm or more and 2.0 μm or less.
Charge Transporting Layer
The charge transporting layer for example, contains a charge transporting material and a binder resin. The charge transporting layer may be a layer that contains a polymer charge transporting material.
Examples of the charge transporting material include electron transporting compounds such as quinone compounds such as p-benzoquinone, chloranil, bromanil, and anthraquinone; tetracyanoquinodimethane compounds; fluorenone compounds such as 2,4,7-trinitrofluorenone; xanthone compounds; benzophenone compounds; cyanovinyl compounds; and ethylene compounds. Other examples of the charge transporting material include hole transporting compounds such as triarylamine compounds, benzidine compounds, aryl alkane compounds, aryl-substituted ethylene compounds, stilbene compounds, anthracene compounds, and hydrazone compounds. These charge transporting materials may be used alone or in combination, but are not limiting.
From the viewpoint of charge mobility, the charge transporting material may be a triaryl amine derivative represented by structural formula (a-1) below or a benzidine derivative represented by structural formula (a-2) below.
In structural formula (a-1), ArT1, ArT2, and ArT3 each independently represent a substituted or unsubstituted aryl group, —C6H4—C(RT4)═C(RT5)(RT6), or —C6H4—CH═CH—CH═C(RT7)(RT8). RT4, RT5, RT6, RT7, and RT8 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group.
Examples of the substituent for each of the groups described above include a halogen atom, an alkyl group having 1 to 5 carbon atoms, and an alkoxy group having 1 to 5 carbon atoms. Examples of the substituent for each of the groups described above include a substituted amino group substituted with an alkyl group having 1 to 3 carbon atoms.
In structural formula (a-2), RT91 and RT92 each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 5 carbon atoms. RT101, RT102, RT111, and RT112 each independently represent a halogen atom, an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, an amino group substituted with an alkyl group having 1 or 2 carbon atoms, a substituted or unsubstituted aryl group, —C(RT12)═C(RT13)(RT14), or —CH═CH—CH═C(RT15)(RT16); and RT12, RT13, RT14, RT15, and RT16 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group. Tm1, Tm2, Tn1, and Tn2 each independently represent an integer of 0 or more and 2 or less.
Examples of the substituent for each of the groups described above include a halogen atom, an alkyl group having 1 to 5 carbon atoms, and an alkoxy group having 1 to 5 carbon atoms. Examples of the substituent for each of the groups described above include a substituted amino group substituted with an alkyl group having 1 to 3 carbon atoms.
Here, among the triarylamine derivatives represented by structural formula (a-1) and the benzidine derivatives represented by structural formula (a-2) above, a triarylamine derivative having —C6H4—CH═CH—CH═C(RT7)(RT8) or a benzidine derivative having —CH═CH—CH═C(RT15)(RT16) may be used from the viewpoint of the charge mobility.
Examples of the polymer charge transporting material that can be used include known charge transporting materials such as poly-N-vinylcarbazole and polysilane. In particular, polyester polymer charge transporting materials may be used. The polymer charge transporting material may be used alone or in combination with a binder resin.
Examples of the binder resin used in the charge transporting layer include polycarbonate resins, polyester resins, polyarylate resins, methacrylic resins, acrylic resins, polyvinyl chloride resins, polyvinylidene chloride resins, polystyrene resins, polyvinyl acetate resins, styrene-butadiene copolymers, vinylidene chloride-acrylonitrile copolymers, vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinyl acetate-maleic anhydride copolymers, silicone resins, silicone alkyd resins, phenol-formaldehyde resins, styrene-alkyd resins, poly-N-vinylcarbazole, and polysilane. Among these, a polycarbonate resin or a polyarylate resin may be used as the binder resin. These binder resins are used alone or in combination.
The blend ratio of the charge transporting material to the binder resin may be in the range of 10:1 to 1:5 on a mass ratio basis.
The charge transporting layer may contain other known additives.
The charge transporting layer may be formed by any known method. For example, a coating film is formed by using a charge-transporting-layer-forming solution prepared by adding the above-mentioned components to a solvent, dried, and, if needed, heated.
Examples of the solvent used to prepare the charge-transporting-layer-forming solution include common organic solvents such as aromatic hydrocarbons such as benzene, toluene, xylene, and chlorobenzene; ketones such as acetone and 2-butanone; halogenated aliphatic hydrocarbons such as methylene chloride, chloroform, and ethylene chloride; and cyclic or linear ethers such as tetrahydrofuran and ethyl ether. These solvents are used alone or in combination as a mixture.
Examples of the method for applying the charge-transporting-layer-forming solution to the charge generating layer include common methods such as a blade coating method, a wire bar coating method, a spray coating method, a dip coating method, a bead coating method, an air knife coating method, and a curtain coating method.
The thickness of the charge transporting layer may be set within the range of, for example, 5 μm or more and 50 μm or less, or within the range of 10 μm or more and 30 μm or less.
Protective Layer
A protective layer is disposed on a photosensitive layer if necessary. The protective layer is, for example, formed to avoid chemical changes in the photosensitive layer in a charged state and further improve the mechanical strength of the photosensitive layer.
Thus, the protective layer may be a layer formed of a cured film (crosslinked film). Examples of such a layer include layers indicated in 1) and 2) below.
1) A layer formed of a cured film of a composition that contains a reactive-group-containing charge transporting material having a reactive group and a charge transporting skeleton in the same molecule (in other words, a layer that contains a polymer or crosslinked body of the reactive-group-containing charge transporting material).
2) A layer formed of a cured film of a composition that contains a non-reactive charge transporting material, and a reactive-group-containing non-charge transporting material that does not have a charge transporting skeleton but has a reactive group (in other words, a layer that contains a polymer or crosslinked body of the non-reactive charge transporting material and the reactive-group-containing non-charge transporting material).
Examples of the reactive group contained in the reactive-group-containing charge transporting material include chain-polymerizable groups, an epoxy group, —OH, —OR (where R represents an alkyl group), —NH2, —SH, —COOH, and —SiRQ13-Qn(ORQ2)Qn (where RQ1 represents a hydrogen atom, an alkyl group, or a substituted or unsubstituted aryl group, RQ2 represents a hydrogen atom, an alkyl group, or a trialkylsilyl group, and Qn represents an integer of 1 to 3).
The chain-polymerizable group may be any radical-polymerizable functional group, and an example thereof is a functional group having a group that contains at least a carbon-carbon double bond. A specific example thereof is a group that contains at least one selected from a vinyl group, a vinyl ether group, a vinyl thioether group, a styryl group (vinylphenyl group), an acryloyl group, a methacryloyl group, and derivatives thereof. Among these, the chain-polymerizable group may be a group that contains at least one selected from a vinyl group, a styryl group (vinylphenyl group), an acryloyl group, a methacryloyl group, and derivatives thereof due to their excellent reactivity.
The charge transporting skeleton of the reactive-group-containing charge transporting material may be any known structure used in the electrophotographic photoreceptor, and examples thereof include skeletons that are derived from nitrogen-containing hole transporting compounds, such as triarylamine compounds, benzidine compounds, and hydrazone compounds, and that are conjugated with nitrogen atoms. Among these, a triarylamine skeleton may be used.
The reactive-group-containing charge transporting material that has such a reactive group and a charge transporting skeleton, the non-reactive charge transporting material, and the reactive-group-containing non-charge transporting material may be selected from among known materials.
The protective layer may contain other known additives.
The protective layer may be formed by any known method. For example, a coating film is formed by using a protective-layer-forming solution prepared by adding the above-mentioned components to a solvent, dried, and, if needed, cured such as by heating.
Examples of the solvent used to prepare the protective-layer-forming solution include aromatic solvents such as toluene and xylene, ketone solvents such as methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone, ester solvents such as ethyl acetate and butyl acetate, ether solvents such as tetrahydrofuran and dioxane, cellosolve solvents such as ethylene glycol monomethyl ether, and alcohol solvents such as isopropyl alcohol and butanol. These solvents are used alone or in combination as a mixture.
The protective-layer-forming solution may be a solvent-free solution.
Examples of the application method used to apply the protective-layer-forming solution onto the photosensitive layer (for example, the charge transporting layer) include common methods such as a dip coating method, a lift coating method, a wire bar coating method, a spray coating method, a blade coating method, a knife coating method, and a curtain coating method.
The thickness of the protective layer may be set within the range of, for example, 1 μm or more and 20 μm or less, or within the range of 2 μm or more and 10 μm or less.
Single-Layer-Type Photosensitive Layer
The single-layer-type photosensitive layer (charge generating/charge transporting layer) is, for example, a layer that contains a charge generating material, a charge transporting material, and, optionally, a binder resin and other known additives. These materials are the same as those described in relation to the charge generating layer and the charge transporting layer.
The amount of the charge generating material contained in the single-layer-type photosensitive layer relative to the total solid content may be 0.1 mass % or more and 10 mass % or less, and is preferably 0.8 mass % or more and 5 mass % or less. The amount of the charge transporting material contained in the single-layer-type photosensitive layer relative to the total solid content may be 5 mass % or more and 50 mass % or less.
The method for forming the single-layer-type photosensitive layer is the same as the method for forming the charge generating layer and the charge transporting layer.
The thickness of the single-layer-type photosensitive layer may be, for example, 5 μm or more and 50 μm or less, or 10 μm or more and 40 μm or less.
Image Forming Apparatus and Process Cartridge
An image forming apparatus of an exemplary embodiment includes an electrophotographic photoreceptor, a charging unit that charges a surface of the electrophotographic photoreceptor, an electrostatic latent image forming unit that forms an electrostatic latent image on the charged surface of the electrophotographic photoreceptor, a developing unit that develops the electrostatic latent image on the surface of the electrophotographic photoreceptor by using a developer that contains a toner so as to form a toner image, and a transfer unit that transfers the toner image onto a surface of a recording medium. The electrophotographic photoreceptor of the exemplary embodiment described above is used as the electrophotographic photoreceptor.
The image forming apparatus of the exemplary embodiment is applied to a known image forming apparatus, examples of which include an apparatus equipped with a fixing unit that fixes the toner image transferred onto the surface of the recording medium; a direct transfer type apparatus with which the toner image formed on the surface of the electrophotographic photoreceptor is directly transferred to the recording medium; an intermediate transfer type apparatus with which the toner image formed on the surface of the electrophotographic photoreceptor is first transferred to a surface of an intermediate transfer body and then the toner image on the surface of the intermediate transfer body is transferred to the surface of the recording medium; an apparatus equipped with a cleaning unit that cleans the surface of the electrophotographic photoreceptor after the toner image transfer and before charging; an apparatus equipped with a charge erasing unit that erases the charges on the surface of the electrophotographic photoreceptor by applying the charge erasing light after the toner image transfer and before charging; and an apparatus equipped with an electrophotographic photoreceptor heating member that elevates the temperature of the electrophotographic photoreceptor to reduce the relative temperature.
In the intermediate transfer type apparatus, the transfer unit includes, for example, an intermediate transfer body having a surface onto which a toner image is to be transferred, a first transfer unit that conducts first transfer of the toner image on the surface of the electrophotographic photoreceptor onto the surface of the intermediate transfer body, and a second transfer unit that conducts second transfer of the toner image on the surface of the intermediate transfer body onto a surface of a recording medium.
The image forming apparatus of this exemplary embodiment may be of a dry development type or a wet development type (development type that uses a liquid developer).
In the image forming apparatus of the exemplary embodiment, for example, a section that includes the electrophotographic photoreceptor may be configured as a cartridge structure (process cartridge) detachably attachable to the image forming apparatus. A process cartridge equipped with the electrophotographic photoreceptor of the exemplary embodiment may be used as this process cartridge. The process cartridge may include, in addition to the electrophotographic photoreceptor, at least one selected from the group consisting of a charging unit, an electrostatic latent image forming unit, a developing unit, and a transfer unit.
Although some examples of the image forming apparatus of an exemplary embodiment are described below, these examples are not limiting. Only relevant sections illustrated in the drawings are described, and descriptions of other sections are omitted.
As illustrated in
The process cartridge 300 illustrated in
Although an example of the image forming apparatus equipped with a fibrous member 132 (roll) that supplies a lubricant 14 to the surface of the electrophotographic photoreceptor 7 and a fibrous member 133 (flat brush) that assists cleaning is illustrated in
The features of the image forming apparatus of this exemplary embodiment will now be described.
Charging Device
Examples of the charging device 8 include contact-type chargers that use conductive or semi-conducting charging rollers, charging brushes, charging films, charging rubber blades, and charging tubes. Known chargers such as non-contact-type roller chargers, and scorotron chargers and corotron chargers that utilize corona discharge are also be used.
Exposing Device
Examples of the exposing device 9 include optical devices that can apply light, such as semiconductor laser light, LED light, or liquid crystal shutter light, into a particular image shape onto the surface of the electrophotographic photoreceptor 7. The wavelength of the light source is to be within the spectral sensitivity range of the electrophotographic photoreceptor. The mainstream wavelength of the semiconductor lasers is near infrared having an oscillation wavelength at about 780 nm. However, the wavelength is not limited to this, and a laser having an oscillation wavelength on the order of 600 nm or a blue laser having an oscillation wavelength of 400 nm or more and 450 nm or less may be used. In order to form a color image, a surface-emitting laser light source that can output multi beams is also effective.
Developing Device
Examples of the developing device 11 include common developing devices that perform development by using a developer in contact or non-contact manner. The developing device 11 is not particularly limited as long as the aforementioned functions are exhibited, and is selected according to the purpose. An example thereof is a known developer that has a function of attaching a one-component developer or a two-component developer to the electrophotographic photoreceptor 7 by using a brush, a roller, or the like. In particular, a development roller that retains the developer on its surface may be used.
The developer used in the developing device 11 may be a one-component developer that contains only a toner or a two-component developer that contains a toner and a carrier. The developer may be magnetic or non-magnetic. Any known developers may be used as these developers.
Cleaning Device
A cleaning blade type device equipped with a cleaning blade 131 is used as the cleaning device 13.
Instead of the cleaning blade type, a fur brush cleaning type device or a development-cleaning simultaneous type device may be employed.
Transfer Device
Examples of the transfer device 40 include contact-type transfer chargers that use belts, rollers, films, rubber blades, etc., and known transfer chargers such as scorotron transfer chargers and corotron transfer chargers that utilize corona discharge.
Intermediate Transfer Body
A belt-shaped member (intermediate transfer belt) that contains semi-conducting polyimide, polyamide imide, polycarbonate, polyarylate, a polyester, a rubber or the like is used as the intermediate transfer body 50. The form of the intermediate transfer body other than the belt may be a drum.
An image forming apparatus 120 illustrated in
The electrophotographic photoreceptor of the present disclosure will now be described more specifically through examples below. The materials, the amounts thereof used, the ratios, the treatment procedure, and the like of the examples described below are subject to modification and alteration without departing from the gist of the present disclosure. Thus, the interpretation of the scope of the electrophotographic photoreceptor of the present disclosure is not to be limited by the specific examples described below.
Preparation of Photoreceptor
The following amine compounds are prepared as the amine compounds used in Examples and Comparative Examples. The ionization potentials (Ip) of the amine compounds are measured with photoelectron spectroscope AC-2 produced by RIKEN KEIKI Co., Ltd.
Amine Compounds for Examples
Amine compound (1): a compound represented by structural formula (1) above (Ip: 5.41 eV)
Amine compound (2): a compound represented by structural formula (2) above (Ip: 5.49 eV)
Amine compound (3): a compound represented by structural formula (3) above (Ip: 5.50 eV)
Amine compound (4): a compound represented by structural formula (4) above (Ip: 5.56 eV)
Amine compound (5): a compound represented by structural formula (5) above (Ip: 5.64 eV)
Amine compound (6): a compound represented by structural formula (6) above (Ip: 5.65 eV)
Amine compound (7): N-2-(aminoethyl)-3-aminopropyltrimethoxysilane (Ip: 5.75 eV)
Amine compound (8): a compound represented by structural formula (7) above (Ip: 5.77 eV)
Amine compound (9): a compound represented by structural formula (8) above (Ip: 5.78 eV)
Amine compound (11): 1,4-diazabicyclo[2.2.2]octane (Ip: 5.87 eV) Amine compounds for Comparative Examples
Amine compound (12): a compound represented by structural formula (9) below (Ip: 5.28 eV)
Amine compound (13): a compound represented by structural formula (10) below (Ip: 5.32 eV)
Amine compound (14): tribenzylamine (Ip: >6.00 eV)
Formation of Undercoat Layer
In 130 parts by mass of methyl ethyl ketone, 19.5 parts by mass of a blocked isocyanate (Sumidur BL3175 produced by Sumitomo Bayer Urethane Co., Ltd., solid content: 75 mass %) and 7.5 parts by mass of a butyral resin (S-LEC BL-1 produced by Sekisui Chemical Co., Ltd.) are dissolved. To the resulting solution, 34 parts by mass of the perinone compound (1-1), 0.9 parts by mass of the amine compound (4), and 0.005 parts by mass of bismuth carboxylate (K-KAT XK-640 produced by King Industries, Inc.) are added, and the resulting mixture is dispersed for 10 hours in a sand mill using glass beads having a diameter of 1 mm so as to obtain a coating solution for an undercoat layer. The molecular weight of the amine compound (4) is 451.6, and the amount of the amine compound (4) contained relative to the solid content in the coating solution is 0.03 mmol/g. The coating solution is applied to a cylindrical aluminum substrate by dip coating, and dried and cured at 160° C. for 60 minutes so as to form an undercoat layer having a thickness of 7 μm.
Formation of Charge Generating Layer
Hydroxygallium phthalocyanine having diffraction peaks at least at Bragg's angles (2θ±0.2°) of 7.5°, 16.3°, 25.0°, and 28.3° in an X-ray diffraction spectrum obtained by using CuKα X-ray is prepared as the charge generating material. A mixture containing 15 parts by mass of hydroxygallium phthalocyanine, 10 parts by mass of a vinyl chloride-vinyl acetate copolymer resin (VMCH produced by Nippon Unicar Company Limited), and 200 parts by mass of n-butyl acetate is dispersed for 4 hours in a sand mill using glass beads having a diameter of 1 mm. To the resulting dispersion, 175 parts by mass of n-butyl acetate and 180 parts by mass of methyl ethyl ketone are added and stirred so as to obtain a charge-generating-layer-forming solution. The solution is applied to the undercoat layer by dip-coating, and heated at 150° C. for 10 minutes to form a charge generating layer having a thickness of 0.2 μm.
Formation of Charge Transporting Layer
To 800 parts by mass of tetrahydrofuran, 38 parts by mass of a charge transporting agent (HT-1), 10 parts by mass of a charge transporting agent (HT-2), and 52 parts by mass of a polycarbonate (A) (viscosity-average molecular weight: 48,000) are added and dissolved, 8 parts by mass of tetraethylene fluoride resin (Lubron L5 produced by Daikin Industries Ltd., average particle diameter: 300 nm) is added, and the resulting mixture is dispersed for 2 hours by using a homogenizer (ULTRA-TURRAX produced by IKA Japan) at 5500 rpm to obtain a charge-transporting-layer-forming solution. The solution is applied to the charge generating layer by dip-coating, and dried at 140° C. for 40 minutes to form a charge transporting layer having a thickness of 26 μm. A photoreceptor of Example 1 is obtained through such a process.
Photoreceptors are prepared as in Example 1 except that, in forming the undercoat layer, the type of the perinone compound, the type of the amine compound, or the amount of the amine compound added is changed as indicated in Table 2.
A photoreceptor is prepared as in Example 1 except that, in forming the undercoat layer, the amine compound (4) is not used.
Photoreceptors are prepared as in Example 1 except that, in forming the undercoat layer, the type of the amine compound and the amount of the amine compound added are changed as indicated in Table 1.
Photoreceptors are prepared as in Comparative Example 1 except that, in forming the undercoat layer, the perinone compound is changed to the imide compound indicated in Table 1. The chemical structures of an imide compound (A), an imide compound (B), and an imide compound (C) used in Comparative Examples A to C are as follows.
A photoreceptor is prepared as in Example 1 except that, in forming the undercoat layer, the binder resin is changed from polyurethane to polyamide, and the process of forming the undercoat layer is changed as below.
Formation of Undercoat Layer
In 120 parts by mass of methanol and 60 parts by mass of isopropanol, 22.5 parts by mass of a polyamide resin CM8000 (produced by Toray Industries, Inc.) is dissolved. To the resulting solution, a mixture of 34 parts by mass of the perinone compound (1-1) and 0.9 parts by mass of the amine compound (4) is added, and the resulting mixture is dispersed for 10 hours in a sand mill using glass beads having a diameter of 1 mm so as to obtain a coating solution for forming an undercoat layer. The coating solution is applied to a cylindrical aluminum substrate by dip-coating, and dried and cured at 110° C. for 40 minutes so as to form an undercoat layer having a thickness of 7 μm.
Photoreceptors are prepared as in Example 1 except that, in forming the undercoat layer, the perinone compound is changed as indicated in Table 3.
Photoreceptors are prepared as in Example 1 except that metal oxide particles indicated in Table 3 are added to the coating solution for forming an undercoat layer.
The zinc oxide particles used in Example 15 are particles obtained by surface-treating untreated zinc oxide particles (volume-average particle diameter: 70 nm, specific surface area: 15 m2/g) with a silane coupling agent (KBE-502, 3-methacryloxypropylmethyldiethoxysilane produced by Shin-Etsu Chemical Co., Ltd.).
The titanium oxide particles used in Example 16 have a volume-average particle diameter of 100 nm.
The tin oxide particles used in Example 17 have a volume-average particle diameter of 80 nm.
Performance Evaluation of Photoreceptors
The photoreceptors of Examples and Comparative Examples are each loaded to an image forming apparatus produced by Fuji Xerox Co., Ltd., DocuCentre C5570, and the following performance evaluation is carried out in an environment having a temperature of 30° C. and a relative humidity of 85%. The results are indicated in Tables 1 to 3.
Leak Resistance
The leak resistance is evaluated by utilizing the phenomenon in which spot-like image defects occur in the photoreceptor as a result of leakage of the current.
An image with a density of 20% is continuously output on 20,000 sheets of A4 paper, and 10 hours later, an image with a density of 20% is output on 10 sheets of A4 paper. Whether spot-like image defects are present is observed with naked eye for all ten sheets, and the extent of the image defects is graded from A to C as follows.
A: No spot-like image defects are found.
B: Less than ten spot-like image defects are found, but the performance is acceptable in actual use.
C: Ten or more spot-like image defects are found, and the performance is unacceptable in actual use.
Charge-Retaining Property
A surface potential probe of a surface potentiometer (Trek 334 produced by Trek Japan Co., Ltd.) is installed at a position 1 mm remote from the surface of the photoreceptor.
After the surface of the photoreceptor is charged to −700 V, the decrease in potential (dark decay) after 0.1 seconds is measured, and the decrease in potential is graded from A to C as follows.
A: The decrease in potential is less than 25 V.
B: The decrease in potential is 25 V or more and less than 50 V.
C: The decrease in potential is 50 V or more.
Environmental Stability of Charge-Retaining Property
The environment having a temperature of 30° C. and a relative humidity of 85% is changed to an environment having a temperature of 15° C. and a relative humidity of 10%, and the charge-retaining property is measured. The difference (the amount of change in potential) in measurement values between the two environments is graded from A to C as follows. A: The amount of change in potential is less than 10 V.
B: The amount of change in potential is 10 V or more and less than 20 V.
C: The amount of change in potential is 20 V or more.
Suppression of Piercing by Foreign Matter
When carbon fibers penetrate through the photosensitive layer and the undercoat layer and reach the aluminum substrate, electric current flows and spot-like image defects occur. This phenomenon is utilized to evaluate suppression of piercing by foreign matter.
To a developer, carbon fibers (average diameter: 7 μm, average length: 50 μm) are added until the density reaches 0.1 mass %, and an image with a density of 20% is continuously output on 20,000 sheets of A4 paper. Subsequently, an image with a density of 20% is output on 10 sheets of A4 paper. Whether spot-like image defects are present is observed with naked eye on the image on the tenth sheet, and the extent of the image defects is graded from A to C as follows.
A: No spot-like image defects are found.
B: Less than ten spot-like image defects are found, but the performance is acceptable in actual use.
C: Ten or more spot-like image defects are found, and the performance is unacceptable in actual use.
The foregoing description of the exemplary embodiments of the present disclosure has been provided for the purposes of illustration and description. It is not intended to be exhaustive or to limit the disclosure 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 disclosure and its practical applications, thereby enabling others skilled in the art to understand the disclosure for various embodiments and with the various modifications as are suited to the particular use contemplated. It is intended that the scope of the disclosure be defined by the following claims and their equivalents.
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