Phthalocyanine composition, process for preparing the same and electrophotographic photoreceptor using the same

BACKGROUND OF THE INVENTION
This invention relates to a novel phthalocyanine composition having high sensitivity, a process for preparing the same, an electrophotographic photoreceptor using the same and a coating solution for a charge generation layer.
As a conventional electrophotographic photoreceptor, there may be mentioned a photoreceptor in which about 50 .mu.m of a selenium (Se) film is formed on a conductive substrate such as aluminum by a vacuum vapor deposition method. However, this Se photoreceptor has a problem that it has sensitivity only up to a wavelength of around 500 nm. Further, there may be mentioned a photoreceptor in which about 50 .mu.m of an Se layer is formed on a conductive substrate, and several .mu.m of a selenium-tellurium (Se-Te) alloy layer is further formed thereon. Whereas this photoreceptor has spectral sensitivity to a longer wavelength as the Te content of the above Se-Te alloy is higher, property of maintaining surface charge becomes worse as the amount of Te added is increased. Thus, there is a serious problem that it cannot be used practically as a photoreceptor.
Also, there may be mentioned the so-called composite two layer type photoreceptor in which a charge generation layer is formed on an aluminum substrate by coating about 1 .mu.m of Chlorocyan Blue or a squaraine derivative, and a charge transport layer is formed thereon by coating 10 to 20 .mu.m of a mixture of polyvinylcarbazole or a pyrazoline derivative and a polycarbonate resin having high insulation resistance. This photoreceptor does not have sensitivity to light of 700 nm or more as a matter of fact.
In recent years, there have been reported many composite two layer type photoreceptors in which the above drawbacks have been cancelled, that is, those having sensitivity to around 800 nm which is the wavelength of a diode laser region. However, in many of these, a phthalocyanine pigment is used as a charge generating material, and on a charge generation layer having a film thickness of about 0.5 to 1 .mu.m, a charge transport layer is formed by coating 10 to 20 .mu.m of a mixture having high insulation resistance of a polyvinylcarbazole, a pyrazoline derivative or a hydrazone derivative and a polycarbonate resin or a polyester resin to form a composite two layer type photoreceptor.
In phthalocyanines, not only absorption spectrum and photoconductivity vary depending on central metals, but also these physical properties vary depending on crystal forms. There have been reported several examples of phthalocyanines in which the same central metal is used, but a specific crystal form is selected for an electrophotographic photoreceptor.
For example, there has been reported that various crystal forms exist in titanylphthalocyanines, and charging characteristics, dark decay and sensitivity vary greatly depending on the difference of their crystal forms.
In Japanese Provisional Patent Publication No. 49544/1984, there has been described that a crystal form of titanylphthalocyanine giving strong diffraction peaks at 9.2.degree., 13.1.degree., 20.7.degree., 26.2.degree. and 27.1.degree. of Bragg angles (2.theta..+-.0.2.degree.) is preferred, and an X-ray diffraction spectrum chart is shown.
Electrophotographic characteristics of a photoreceptor using the titanylphthalocyanine having the crystal form as a charge generating material are dark decay (DDR) of 85% and sensitivity (E.sub.1/2) of 0.57 lux.cndot.sec.
Also, in Japanese Provisional Patent Publication No. 166959/1984, a charge generation layer is obtained by allowing a vapor deposited film of titanylphthalocyanine to stand in tetrahydrofuran-saturated vapor for 1 to 24 hours to change a crystal form. It has been shown that the X-ray diffraction spectrum gives strong diffraction peaks at 7.5.degree., 12.6.degree., 13.0.degree., 25.4.degree., 26.2.degree. and 28.6.degree. of Bragg angles (2.theta.).
Electrophotographic characteristics of a photoreceptor using the titanylphthalocyanine having the crystal form as a charge generating material are dark decay (DDR) of 86% and sensitivity (E.sub.1/2) of 0.7 lux.cndot.sec.
Further, in Japanese Provisional Patent Publication No. 17066/1989, there has been described that a crystal form of titanylphthalocyanine having main peaks at least at 9.5.degree., 9.7.degree., 11.7.degree., 15.0.degree., 23.5.degree., 24.1.degree. and 27.3.degree. of Bragg angles (2.theta..+-.0.2.degree.) is preferred.
In Japanese Provisional Patent Publications No. 131243/1990 and No. 214867/1990, there has been described that a crystal form of titanylphthalocyanine having a main diffraction peak at 27.3.degree. of Bragg angles is preferred.
Electrophotographic characteristics of a photoreceptor using the titanylphthalocyanine having the crystal form described in Japanese Provisional Patent Publications No. 131243/1990 as a charge generating material are dark decay (DDR) of 77.2% and sensitivity (E.sub.1/2) of 0.38 lux.cndot.sec.
Thus, the phthalocyanines are different in electrophotographic properties depending on the difference of crystal forms and the crystal form is an important factor for deciding characteristics of an electrophotographic photoreceptor.
In Japanese Provisional Patent Publication No. 255456/1991, there has been reported an example using two kinds or more of phthalocyanines and described an example using a mixture of titanylphthalocyanine and a non-metal phthalocyanine as a charge generating material.
As described above, titanylphthalocyanine exhibits extremely high sensitivity and excellent characteristics by changing a crystal form. However, in a laser printer for which it is used, higher quality and higher precision have been achieved, and an electrophotographic photoreceptor having further high sensitivity characteristic has been demanded.
SUMMARY OF THE INVENTION
An object of the present invention is to provide a phthalocyanine composition having high sensitivity, a process for preparing the same, an electrophotographic photoreceptor using the same and a coating solution for a charge generation layer.
The present invention relates to a phthalocyanine composition which comprises having main diffraction peaks at 7.5.degree., 22.5.degree., 24.3.degree., 25.3.degree. and 28.6.degree. of Bragg angles (2.theta..+-.0.2.degree.) in an X-ray diffraction spectrum with Cu K.alpha. and a coating solution for a charge generation layer.
Also, the present invention relates to a process for preparing a phthalocyanine composition having main diffraction peaks at 7.5.degree., 22.5.degree., 24.3.degree., 25.3.degree. and 28.6.degree. of Bragg angles (2.theta..+-.0.2.degree.) in an X-ray diffraction spectrum with Cu K.alpha., which comprises making a phthalocyanine mixture containing a titanylphthalocyanine and a halogenated metal phthalocyanine in which a central metal is trivalent, and being amorphous, and then treating the amorphous mixture with an organic solvent.
Generally speaking, a phthalocyanine mixture is a mere physical mixture of two more more phthalocyanines used as starting materials, and an X-ray diffraction pattern of the phthalocyanine mixture comprises piled up (sum) peak patterns of respective phthalocyanines used as starting materials. On the other hand, the phthalocyanine mixture of the present invention is that phthalocyanines used as starting materials are mixed in a molecular order and an X-ray diffraction pattern thereof is different from that of a pattern in which peak patterns of the respective phthalocyanines used as starting materials are piled up.
In another embodiment of the present invention, a process for preparing a phthalocyanine composition comprises making a phthalocyanine mixture containing titanylphthalocyanine and a halogenated metal phthalocyanine in which a central metal is trivalent, and being amorphous by an acid pasting method, washing the amorphous mixture of precipitates with water until the washed water has a pH of 3 to 6 and a conductivity of 10 to 300 .mu.S/cm, preferably 10 to 200 .mu.S/cm, more preferably 10 to 100 .mu.S/cm, and then treating the amorphous mixture with an organic solvent.
Further, an electrophotographic photoreceptor of the present invention comprises, in an electrophotographic photoreceptor having a photoconductive layer containing an organic photoconductive substance on a conductive substrate, said organic photoconductive substance being a phthalocyanine composition having main diffraction peaks at 7.5.degree., 22.5.degree., 24.3.degree., 25.3.degree. and 28.6.degree. of Bragg angles (2.theta..+-.0.2.degree.) in an X-ray diffraction spectrum with Cu K.alpha..
In an additional embodiment of the present invention, an electrophotographic photoreceptor comprises a conductive substrate and a photoconductive layer containing an organic photoconductive substance formed on the substrate, wherein said organic photoconductive substance is a phthalocyanine composition prepared by making a phthalocyanine mixture containing a titanylphthalocyanine and a halogenated metal phthalocyanine in which a central metal is trivalent, and being amorphous by an acid pasting method, washing the amorphous precipitates until a washed water has a pH of 3 to 6 and a conductivity is 10 to 300 .mu.S/cm, preferably 10 to 200 .mu.S/cm, more preferably 10 to 100 .mu.S/cm, and then treating the precipitates with an organic solvent.
Moreover, the present invention relates to a double-layered type electrophotographic photoreceptor which comprises a charge generation layer containing the phthalocyanine composition described above as a charge generating material, and a charge transport layer containing a benzidine derivative represented by the following formula (I): ##STR1## wherein R.sub.1 and R.sub.2 each independently represent hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an aryl group, a fluoroalkyl group or a fluoroalkoxy group, two R.sub.3 s each independently represents a hydrogen atom or an alkyl group, Ar.sub.1 and Ar.sub.2 each independently represents an aryl group, and k, l, m, and n each independently represents an integer of 0 to 5.

BRIEF DESCRIPTION OF THE DRAWING
FIG. 1 is an X-ray diffraction spectrum of a phthalocyanine composition treated with N-methyl-2-pyrrolidone in Example 1.
FIG. 2 is an X-ray diffraction spectrum of titanylphthalocyanine treated with N-methyl-2-pyrrolidone in Comparative example 1.
FIG. 3 is an X-ray diffraction spectrum of chloroindium phthalocyanine treated with N-methyl-2-pyrrolidone in Comparative example 2.
FIG. 4 is an X-ray diffraction spectrum of a mixture of titanylphthalocyanine and chloroindium phthalocyanine which is made amorphous with sulfuric acid in Comparative example 3.
FIG. 5 is an X-ray diffraction spectrum of phthalocyanine compositions treated with methyl ethyl ketone in Examples 5 to 8.
FIG. 6 is an X-ray diffraction spectrum of titanylphthalocyanine treated with methyl ethyl ketone in Comparative example 4.
FIG. 7 is an X-ray diffraction spectrum of chloroindium phthalocyanine treated with methyl ethyl ketone in Comparative example 5.

DESCRIPTION OF THE PREFERRED EMBODIMENTS
In the following, the present invention is described in detail.
The titanylphthalocyanine to be used in the present invention can be obtained by referring to, for example, the description of Japanese Provisional Patent Publication No. 71144/1991, and can be prepared, for example, as mentioned below.
To 120 ml of .alpha.-chloronaphthalene is added 18.4 g (0.144 mole) of phthalonitrile, and then 4 ml (0.0364 mole) of titanium tetrachloride is added dropwise to the mixture under nitrogen atmosphere. After the dropwise addition, the mixture is heated and reacted at 200.degree. to 220.degree. C. for 3 hours under stirring, and then the reaction mixture is filtered while heating at 100.degree. to 130.degree. C. and the residue is washed successively with .alpha.-chloronaphthalene and then with methanol. The residue is hydrolyzed (90.degree. C., 1 hour) with 140 ml of a deionized water, and this operation is repeated until the solution becomes neutral. The residue is then washed with methanol. Subsequently, the residue was successively washed with 200 ml of N-methyl-2-pyrrolidone heated to 100.degree. C. and then with methanol. The compound thus obtained is dried by heating at 60.degree. C. under vacuum to obtain titanylphthalocyanine (yield: 46%).
In the halogenated metal phthalocyanine compounds in which a central metal is trivalent to be used in the present invention, a trivalent metal as a central metal includes In, Ga and Al, a halogen includes Cl and Br, and said compounds may have a substituent(s) such as a halogen on a phthalocyanine ring. Said compounds are known compounds, and among them, for example, a synthetic method of monohalogen metal phthalocyanine and monohalogen metal halogen phthalocyanine is described in Inorganic Chemistry, 19, 3131 (1980) and Japanese Provisional Patent Publication No. 44054/1984.
The monohalogen metal phthalocyanine can be prepared by, for example, the following manner.
To 100 ml of quinoline distilled twice and deoxidized are added 78.2 mmole of phthalonitrile and 15.8 mmole of metal trihalide, and the mixture is refluxed under heating for 0.5 to 3 hours. After gradually cooled, the mixture is cooled to 0.degree. C. and then filtered. The crystal is washed successively with methanol, toluene and then acetone, and dried at 110.degree. C.
Further, the monohalogen metal halogen phthalocyanine can be prepared by, for example, the following manner. After 156 mmole of phthalonitrile and 37.5 mmole of metal trihalide are mixed and melted at 300.degree. C., the mixture is heated for 0.5 to 3 hours to obtain a crude product of monohalogen metal halogen phthalocyanine. The product is washed with .alpha.-chloronaphthalene by using a Soxhlet extractor.
In the present invention, as to a composition ratio of the phthalocyanine mixture containing a titanylphthalocyanine and a halogenated metal phthalocyanine in which a central metal is trivalent, the content of the titanylphthalocyanine is preferably in the range of 20 to 95% by weight, more preferably in the range of 50 to 90% by weight, particularly preferably in the range of 65 to 90% by weight, most preferably in the range of 75 to 90% by weight from the point of electrophotographic characteristics such as charging characteristics, dark decay and sensitivity.
The phthalocyanine mixture can be made amorphous by the acid pasting method.
For example, 1 g of the phthalocyanine mixture is dissolved in 50 ml of conc. sulfuric acid, and the solution is added dropwise to 1 liter of pure water cooled with ice water to be reprecipitated. After filtration, the precipitates are washed sufficiently with pure water and then with a mixed solution of methanol/pure water, and then dried at 110.degree. C. to obtain powder of a phthalocyanine composition. The X-ray diffraction spectrum of the phthalocyanine composition thus obtained becomes a spectrum having no clear sharp peak and showing wide amorphous state. As a method of making it amorphous, in addition to the acid paste method using conc. sulfuric acid, there is also a method by dry milling.
Or else, the following method may be employed. That is, 1 g of the phthalocyanine mixture is dissolved in 50 ml of conc. sulfuric acid, and the mixture is stirred at room temperature. Subsequently, the mixture is added dropwise to 1 liter of a deionized water cooled with ice water over about 1 hour, preferably 40 minutes to 50 minutes to be reprecipitated. After left to stand overnight, the supernatant is removed by decantation, and then the precipitates are collected by centrifugation. Thereafter, the precipitates are washed repeatedly with a deionized water which is a washing water until the washing water after washing has a pH of 3 to 6 and a conductivity of 5 to 300 .mu.S/cm, preferably 5 to 200 .mu.S/cm, more preferably 5 to 100 .mu.S/cm. Then, the precipitates are washed sufficiently with methanol, and dried by heating at 60.degree. C. under vacuum to obtain powder of a phthalocyanine composition.
If the pH is less than 3 or exceeds 6, charging characteristics, dark decay and sensitivity are poor, while if the conductivity is less than 5 .mu.S/cm or exceeds 300 .mu.S/cm, charging characteristics, dark decay and sensitivity are poor.
By treating the phthalocyanine mixture which is thus made amorphous with an organic solvent to change crystal form as mentioned below, the phthalocyanine composition having specific diffraction peaks of the present invention can be obtained.
For example, 1 g of powder of the phthalocyanine mixture which is made amorphous is added to 10 ml of an organic solvent such as methyl ethyl ketone and N-methyl-2-pyrrolidone, and the mixture is heated and stirred (the above powder/solvent (in terms of weight ratio) is 1/1 to 1/100). The heating temperature is 50.degree. C. to 200.degree. C., preferably 80.degree. C. to 150.degree. C., and the heating time is 1 hour to 12 hours, preferably 1 hour to 6 hours. After completion of the heating and stirring, the mixture is filtered, and the residue is washed with methanol and dried by heating at 60.degree. C. under vacuum to obtain 700 mg of crystal of the phthalocyanine composition of the present invention. As the organic solvent to be used in the present invention, there may be mentioned, for example, alcohols such as methanol, ethanol, isopropanol and butanol, alicyclic hydrocarbons such as n-hexane, octane and cyclohexane, aromatic hydrocarbons such as benzene, toluene and xylene, ethers such as tetrahydrofuran, dioxane, diethyl ether, ethylene glycol dimethyl ether, 2-methoxyethanol and ethylene glycol diethyl ether, ketones such as acetone, methyl ethyl ketone, cyclohexanone and isophorone, esters such as methyl acetate and ethyl acetate, non-chlorine type organic high polar solvents such as dimethyl sulfoxide, dimethylformamide, phenol, cresol, anisole, nitrobenzene, acetophenone, benzyl alcohol, pyridine, N-methyl-2-pyrrolidone, quinoline, tetralin and picoline and halogen type organic solvents such as dichloromethane, dichloroethane, trichloroethane, tetrachloroethane, carbon tetrachloride, chloroform, chloromethyloxirane, chlorobenzene and dichlorobenzene.
Among these, aromatic hydrocarbons, ketones and non-chlorine type organic solvents are preferred, and particularly, N-methyl-2-pyrrolidone, pyridine, methyl ethyl ketone, diethyl ketone, toluene, and tetralin are preferred.
The electrophotographic photoreceptor according to the present invention has a photoconductive layer provided on a conductive substrate.
In the present invention, the photoconductive layer is a layer containing an organic photoconductive substance, including a film of an organic photoconductive substance, a film containing an organic photoconductive substance and a binder, and a double-layered type film comprising a charge generation layer and a charge transport layer.
As the above organic photoconductive substance, the above phthalocyanine composition is used as an indispensable component, and further known pigments may be used in combination. Further, as the organic photoconductive substance, the above phthalocyanine composition is preferably used in combination of an organic pigment which generates a charge and/or a charge transport substance. The above charge generation layer contains said phthalocyanine composition and/or an organic pigment which generates a charge, and the charge transport layer contains a charge transport substance.
As the above organic pigment which generates a charge, there may be used pigments which have been known to generate a charge, such as metallic or non-metallic type phthalocyanine having various crystalline structures, for example, .alpha. type, .beta. type, .gamma. type, .delta. type, .epsilon. type and .chi. type. The above organic pigments may include azo pigments, anthraquinone pigments, indigoid pigments, quinacridone pigments, perillene pigments, polycyclic quinone pigments and methine pigments and have been disclosed in, for example, Japanese Provisional Patent Publications No. 37543/-1972, No. 37544/1972, No. 18543/1972, No. 18544/1972, No. 43942/1973, No. 70538/1973, No. 1231/1974, No. 105536/1974, No. 75213/1975, No. 44028/1978 and No. 17732/1979.
Further, .tau., .tau.', .eta. and .eta.' type non-metallic phthalocyanines as disclosed in Japanese Provisional Patent Publication No. 182640/1983 and European Patent Publication No. 92,255 may be used. In addition to those described above, any organic pigment which generates a charge by irradiation of light may be used.
As the above charge transport substance, there may be mentioned a polymeric compound such as poly-N-vinylcarbazole, halogenated poly-N-vinylcarbazole, polyvinyl pyrene, polyvinyl indoloquinoxaline, polyvinyl benzothiophene, polyvinyl anthracene, polyvinyl acridine and polyvinyl pyrazoline, and a monomeric compound such as fluorenone, fluorene, 2,7-dinitro-9-fluorenone, 4H-indeno(1,2,6)-thiophen-4-one, 3,7-dinitro-dibenzothiophene-5-oxide, 1-bromopyrene, 2-phenylpyrene, carbazole, N-ethylcarbazole, 3-phenylcarbazole, 3-(N-methyl-N-phenylhydrazone)methyl-9-ethylcarbazole, 2-phenylindole, 2-phenylnaphthalene, oxadiazole, 2,5-bis(4-diethylaminophenyl)-1,3,4-oxadiazole, 1-phenyl-3-(4-diethylaminostyryt)-5-(4-diethylaminostyryl)-5-(4-diethylaminophenyl) pyrazoline, 1-phenyl-3-(p-diethylaminophenyl) pyrazoline, p-(dimethylamino)-stilbene, 2-(4-dipropylaminophenyl) -4 -(4-dimethylaminophenyl)-5-(2-chlorophenyl) -1,3-oxazole, 2-(4-dimethylaminophenyl)-4-(4-dimethylaminophenyl) -5-(2-fluorophenyl)-1,3-oxazole, 2-(4-diethylaminophenyl) -4-(4-dimethylaminophenyl)-5-(2-fluorophenyl)-1,3-oxazole, 2-(4-dipropylaminophenyl)-4-(4-dimethylaminophenyl) -5-(2-fluorophenyl)-1,3-oxazole, imidazole, chrysene, tetraphene, acridene, triphenylamine, benzidine and derivatives thereof. As the charge transport substance, the benzidine derivative represented by the above formula (I) is particularly preferred.
In the formula (I), the alkyl group may include those having 1 to 4 carbon atoms such as a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group and a tert-butyl group. The alkoxy group may include those having 1 to 3 carbon atoms such as a methoxy group, an ethoxy group, an n-propoxy group and an iso-propoxy group. The aryl group may include a phenyl group, a tolyl group, a biphenyl group, a terphenyl group and a naphthyl group. The fluoroalkyl group may include those having 1 to 3 carbon atoms such as a trifluoromethyl group, a trifluoroethyl group and a heptafluoropropyl group. The fluoroalkoxy group may include those having 1 to 4 carbon atoms such as a trifluoromethoxy group, a 2,3-difluoroethoxy group, a 2,2,2-trifluoroethoxy group, a 1H, 1H-pentafluoropropoxy group, a hexafluoro-iso-propoxy group, a 1H, 1H-pentafluorobutoxy group, a 2,2,3,4,4,4-hexafluorobutoxy group and a 4,4,4-trifiuorobutoxy group. Specific examples of the benzidine derivative represented by the formula (I) may include, for example, Compounds No. 1 to No. 6 shown below. ##STR2##
When a mixture of the above phthalocyanine composition and, if necessary, the organic pigment which generates a charge (these are called the former), and the charge transport substance (this is called the latter) is used (when a single layer type photoconductive layer is formed), a weight ratio of the latter/the former to be formulated is preferably within the range of 10/1 to 2/1. Here, a binder is preferably used in an amount of 0 to 500% by weight, particularly in the range of 30 to 500% by weight based on the total amount of these compounds (the former + the latter). When the binder is used, an additive such as a plasticizer, a flowability imparting agent and a pinhole preventing agent may be further added, if necessary.
When the double-layer type photoconductive layer comprising the charge generation layer and the charge transport layer is formed, the charge generation layer contains the above phthalocyanine composition and, if necessary, the organic pigment which generates a charge. A binder may be contained in the charge generation layer in an amount of 0 to 500% by weight, preferably 30 to 500% by weight based on the total amount of the phthalocyanine composition and the organic pigment, and the above additives may be added in an amount of 0.1 to 5% by weight, preferably 0.1 to 2% by weight based on the total amount of the phthalocyanine composition and the organic pigment. Further, in the charge transport layer, the charge transport substance described above is contained, and a binder may be contained in an amount of 30 to 500% by weight, preferably 50 to 300% by weight based on the charge transport substance. When the charge transport substance is a monomeric compound, a binder is preferably contained in an amount of 50 to 500% by weight, preferably 50 to 300% by weight based on said compound.
As the binder which can be used for all cases described above, there may be mentioned a silicone resin, a polyamide resin, a polyurethane resin, a polyester resin, a polyvinyl butyral, an epoxy resin, a polyketone resin, a polycarbonate resin, a polyacrylic resin, a polystyrene resin, a styrene-butadiene copolymer, a poly(methyl methacrylate) resin, a polyvinyl chloride, an ethylene-vinyl acetate copolymer, a vinyl chloride-vinyl acetate copolymer, a polyacrylamide resin, a polyvinylcarbazole, a polyvinyl pyrazoline, a polyvinyl pyrene and a melamine resin. Further, a thermosetting resin and a photocuring resin which are crosslinked by heat and/or light may be also used.
A thermosetting resin comprising a polyvinyl butyral and a melamin resin in combination is preferred since it has high strength, high abrasion resistance and low hygroscopicity.
In either case, the binder is not particularly limited so long as it is a resin which has insulation property and can form a film under normal conditions, and/or a resin which is cured by heat and/or light to form a film.
The plasticizer which is the additive described above may include paraffin halide, dimethylnaphthalene and dibutylphthalate, the flowability imparting agent may include Modaflow (trade name, produced by Monsant Chemical Co.) and Akulonal 4F (trade name, produced by BASF Co.), and the pinhole preventing agent may include benzoin and dimethylphthalate. These may be suitably selected and used, and the amounts thereof may be suitably determined.
In the present invention, the conductive substrate is a conductive member such as a paper or a plastic film subjected to conductive treatment, a plastic film on which a metal foil such as aluminum is laminated and a metal plate.
The electrophotographic photoreceptor of the present invention comprises a photoconductive layer formed on a conductive substrate. The thickness of the photoconductive layer is preferably 5 to 50 .mu.m. When a double-layered type photoconductive layer comprising a charge generation layer and a charge transport layer is used, the charge generation layer preferably has a thickness of 0.001 to 10 .mu.m, particularly preferably 0.2 to 5 .mu.m. If it is less than 0.001 .mu.m, it is difficult to form the charge generation layer uniformly, while if it exceeds 10 .mu.m, electrophotographic characteristics tend to be lowered. The thickness of the charge transport layer is preferably 5 to 50 .mu.m, particularly preferably 8 to 25 .mu.m. If the thickness is less than 5 .mu.m, initial potential is lowered, while if it exceeds 50 .mu.m, sensitivity tends to be lowered.
In order to form the photoconductive layer on the conductive substrate, there may be employed a method in which an organic photoconductive substance is vapor deposited on a conductive substrate, and a method in which an organic photoconductive substance and, if necessary, other components are uniformly dissolved or dispersed in an aromatic solvent such as toluene and xylene, a ketone type solvent such as methyl ethyl ketone, methyl n-propyl ketone and methyl isobutyl ketone, an ether type solvent such as tetrahydrofuran and dioxane, a halogenic type solvent such as methylene chloride, 1,2-dichloroethane and carbon tetrachloride or an alcoholic solvent such as methanol, ethanol and propanol, and the resulting mixture is coated on a conductive substrate and dried. From environmental hygienics view point, a non-halogenic solvent such as an aromatic type solvent, a ketone type solvent, an ether type solvent and an alcoholic type solvent is preferably used. As a coating method, a spin coating method and a dip coating method may be employed. The charge generation layer and the charge transport layer may be formed in the same manner. In that case, either of the charge generation layer or the charge transport layer may be an upper layer, or the charge generation layer may be sandwiched between two layers of the charge transport layers.
When the phthalocyanine composition of the present invention is coated by the spin coating method, it is preferred that spin coating is carried out at a rotation number of 500 to 4,000 rpm, preferably 500 to 2,000 rpm by using a coating solution obtained by dispersing the phthalocyanine composition in a halide solvent such as dichloroethane and dichloromethane, or a non-halide solvent such as toluene or tetrahydrofuran. Further, when the composition is coated by the dip coating method, it is preferred that the conductive substrate is immersed in a coating solution obtained by dispersing the phthalocyanine composition in a solvent such as methanol, dimethylformamide, chloroform, methylene chloride and 1,2-dichloroethane by using a ball mill or ultrasonic wave.
The electrophotographic photoreceptor according to the present invention may further have a thin adhesive layer or a barrier layer immediately on the conductive substrate, or may have a protective layer on the surface.
EXAMPLES
In the following, the present invention is described in detail by referring to Examples and Preparation examples.
Example 1
In 50 ml of sulfuric acid was dissolved 1 g of a phthalocyanine mixture comprising 0.75 g of titanylphthalocyanine and 0.25 g of chloroindium phthalocyanine, and the mixture was added dropwise to 1 liter of pure water cooled with ice water to be reprecipitated. After filtration, the precipitates were washed sufficiently with pure water and then with a mixed solution of methanol/pure water, and then dried at 110.degree. C. to obtain powder.
To 10 ml of N-methyl-2-pyrrolidone was added 1 g of this powder, and the mixture was heated and stirred (150.degree. C., 1 hour). After filtration, the residue was washed with methanol and dried at 60.degree. C. under vacuum to obtain 0.78 g of crystal of the phthalocyanine composition of the present invention. The X-ray diffraction spectrum of this crystal is shown in FIG. 1.
1.5 g of the above phthaiocyanine composition, 1 g of a silicone resin KR-255 (trade name, produced by Shinetsu Kagaku Kogyo Co.) and 98 g of 1,2-dichloroethane were mixed, and the mixture was dispersed by a planetary ball mill. The dispersion obtained was coated on an aluminum plate (conductive substrate, 100 mm.times.100 mm.times.0.l mm) by the dip coating method, and dried at 140.degree. C. for 1 hour to form a charge generation layer having a thickness of 0.5 .mu.m.
A coating solution obtained by mixing 1.5 g of the above charge transport substance No. 1, 1.5 g of a polycarbonate resin Upilon S-3000 trade name, produced by Mitsubishi Gas Kagaku Co.) and 15.5 g of methylene chloride was coated on the above substrate by the dip coating method, and dried at 120.degree. C. for 1 hour to form a charge transport layer having a thickness of 20 .mu.m.
The electrophotographic characteristics of this electrophotographic photoreceptor were measured by an electrostatic copying paper testing device Model SP-428 (trade name, manufactured by Kawaguchi Denki Co.). The photoreceptor was charged by corona discharging of -5 kV under dark condition, and initial charge V.sub.0 (-V) after 10 seconds, dark decay DDR (%) after 30 seconds and white light sensitivity E.sub.1/2 (lux.cndot.sec) when exposed to white light with a luminosity of 2 lux were determined.
A spectral sensitivity was measured by Cynthia 30HC (trade name, manufactured by GENTEC). An irradiation energy required for reducing a surface potential by half 0.2 second after exposure with an initial surface potential of -700 V, an exposure wavelength of 780 nm and an exposure time of 50 mS, i.e. a spectral sensitivity E.sub.50 (.mu.J/cm.sup.2) was measured.
A resolution of photoreceptor was measured as follows. That is, an electrophotographic photoreceptor after measuring electrophotographic characteristics was so charged as to have a surface potential of -600 to -700 V by corona charging, then subjected to image-wise exposure with 100 lux.cndot.sec using Electrophotographic Association of Japan, Chart No. 1-T as an original image, developed with a toner charged to positive, transferred the prepared toner image to a white paper, fixed to effect an examination, and fixed to obtain a test image and evaluated with fine lines number which could be distinguished per 1 mm. The same toner and the same transfer and fixing methods are used in the respective tests. A resolution of photoreceptor immediately after preparation (initial) of a photographic photoreceptor and a resolution of photoreceptor in which corona charging (a surface potential: -1000 V.+-.100 V) and discharging by illumination (light of a wavelength of 500 nm was irradiated with an exposure dose of 10 .mu.J/cm.sup.2) had been repeated 10.sup.4 times were evaluated.
Examples 2 to 4
Crystals were prepared according to Example 1 except for changing the composition ratio of titanylphthalocyanine and chloroindium phthalocyanine of Example 1 as shown in Table 1.
Comparative Example 1
Crystal was prepared according to Example 1 except for using only titanylphthalocyanine in place of the phthalocyanine mixture of Example 1. The X-ray diffraction spectrum of this crystal is shown in FIG. 2.
Comparative Example 2
Crystal was prepared according to Example 1 except for using only chloroindium phthalocyanine in place of the phthalocyanine composition of Example 1. The X-ray diffraction spectrum of this crystal is shown in FIG. 3.
Comparative Example 3
In 50 ml of sulfuric acid was dissolved 1 g of a phthalocyanine mixture comprising 0.75 g of titanylphthalocyanine and 0.25 g of chlcroindium phthalocyanine, and the mixture was added dropwise to 1 liter of pure water cooled with ice water to be reprecipitated. After filtration, the precipitates were washed with pure water and then with a mixed water of methanol/pure water, and then dried at 110.degree. C. to obtain powder. The X-ray diffraction spectrum of this powder is shown in FIG. 4. Electrophotographic characteristics are evaluated in accordance with Example 1.
The electrophotographic characteristics of Examples 1 to 4 and Comparative examples 1 to 3 are shown in Table 1.
TABLE 1__________________________________________________________________________ White Resolution light sen- Spectral (line/mm) Initial Dark sitivity sensitiv- Charging.dis- TiOPc InPcCl charge dacay E.sub.1/2 ity E.sub.50 charging after (wt %) (wt %) V.sub.0 (-V) DDR (%) (lux .multidot. sec) (.mu.J/cm.sup.2) Initial 10.sup.4 times__________________________________________________________________________Example 1 75 25 1020 66.9 0.8 0.30 12.5 12.5Example 2 90 10 1040 66.7 0.8 0.32 12.5 12.5Example 3 25 75 850 44.7 1.2 0.66 12.5 10.0Example 4 50 50 880 43.2 1.0 0.57 12.5 10.0Comparative 100 0 1010 45.5 1.3 0.72 12.5 6.3example 1Comparative 0 100 820 43.9 3.0 1.54 12.5 6.3example 2Comparative 75 25 320 5.0 -- -- 3.2 1.6example 3__________________________________________________________________________
Examples 5 to 8
Crystals were prepared according to Examples 1 to 4 except for carrying out treatment with an organic solvent by using methyl ethyl ketone in place of N-methyl-2-pyrrolidone used in Examples 1 to 4. The X-ray diffraction spectrum of these crystals is shown in FIG. 5.
Comparative Examples 4 and 5
Crystals were prepared according to Comparative examples 1 and 2 except for carrying out treatment with an organic solvent by using methyl ethyl ketone in place of N-methyl-2-pyrrolidone used in Comparative examples 1 and 2. The X-ray diffraction spectra of these crystals are shown in FIGS. 6 and 7, respectively.
The electrophotographic characteristics of Examples 5 to 8 and Comparative examples 4 and 5 are shown in Table 2.
TABLE 2__________________________________________________________________________ White Resolution light sen- Spectral (line/mm) Initial Dark sitivity sensitiv- Charging.dis- TiOPc InPcCl charge dacay E.sub.1/2 ity E.sub.50 charging after (wt %) (wt %) V.sub.0 (-V) DDR (%) (lux .multidot. sec) (.mu.J/cm.sup.2) Initial 10.sup.4 times__________________________________________________________________________Example 5 75 25 920 64.3 0.6 0.26 12.5 12.5Example 6 90 10 920 55.7 0.5 0.24 12.5 12.5Example 7 25 75 670 19.4 1.0 0.60 10.0 10.0Example 8 50 50 740 21.6 0.8 0.46 10.0 10.0Comparative 100 0 660 9.1 2.6 1.42 6.3 3.2example 4Comparative 0 100 600 16.7 3.2 1.73 10.0 4.0example 5__________________________________________________________________________
Examples 9 to 12
Crystals and electrophotographic photoreceptors using the crystals were prepared according to Examples 1 to 4 except for using bromoindium phthalocyanine in place of chloroindium phthalocyanine used in Examples 1 to 4, and using the above charge transport substance No. 2 in place of the above charge transport substance No. 1 as a charge transport material.
Comparative Example 6
An electrophotographic photoreceptor was prepared according to Comparative example 1 except for using the above charge transport substance No. 2 in place of the above charge transport substance No. 1 used in Comparative example 1 as a charge transport material
Comparative Example 7
Crystal and an electrophotographic photoreceptor using the crystal were prepared according to Comparative example 2 except for using bromoindium phthalocyanine in place of chloroindium phthaiocyanine used in Comparative example 2, and using the above charge transport substance No. 2 in place of the above charge transport substance No. 1 as a charge transport material.
Comparative Example 8
Powder was prepared according to Comparative example 3 except for using bromoindium phthalocyanine in place of chloroindium phthalocyanine used in Comparative example 3, and an electrophotographic photoreceptor was prepared by using the powder. The X-ray diffraction spectrum of the powder was the same as that of FIG. 4.
The electrophotographic characteristics of Examples 9 to 12 and Comparative examples 6 to 8 are shown in Table 3.
TABLE 3__________________________________________________________________________ White Resolution light sen- Spectral (line/mm) Initial Dark sitivity sensitiv- Charging.dis- TiOPc InPcCl charge dacay E.sub.1/2 ity E.sub.50 charging after (wt %) (wt %) V.sub.0 (-V) DDR (%) (lux .multidot. sec) (.mu.J/cm.sup.2) Initial 10.sup.4 times__________________________________________________________________________Example 9 75 25 820 69.7 0.7 0.28 12.5 12.5Example 10 90 10 880 57.1 0.9 0.37 12.5 12.5Example 11 25 75 770 44.2 1.4 0.77 12.5 10.0Example 12 50 50 810 45.0 1.1 0.65 12.5 10.0Comparative 100 0 990 44.9 1.4 0.72 10.0 6.3example 6Comparative 0 100 750 42.1 3.2 1.71 10.0 4.0example 7Comparative 75 25 300 5.7 -- -- 3.2 1.6example 8__________________________________________________________________________
Examples 13 to 16
Crystals and electrophotographic photoreceptors using the crystals were prepared according to Examples 1 to 4 except for using chlorogallium phthalocyanine in place of chloroindium phthalocyanine used in Examples 1 to 4, and using the above charge transport substance No. 3 in place of the above charge transport substance No. 1 as a charge transport material.
Comparative Example 9
An electrophotographic photoreceptor was prepared according to Comparative example 1 except for using the above charge transport substance No. 3 in place of the above charge transport substance No. 1 used in Comparative example 1 as a charge transport material
Comparative Example 10
Crystal and an electroohotographic photoreceptor using the crystal were prepared according to Comparative example 2 except for using chlorogallium phthalocyanine in place of chloroindium phthalocyanine used in Comparative example 2, and using the above charge transport substance No. 3 in place of the above charge transport substance No. 1 as a charge transport material.
Comparative Example 11
Powder was prepared according to Comparative example 3 except for using chlorogallium phthalocyanine in place of chloroindium phthaiocyanine used in Comparative example 3, and an electrophotograohic photoreceptor was prepared by using the powder. The X-ray diffraction spectrum of the powder was the same as that of FIG. 4.
The electrophotographic characteristics of Examples 13 to 16 and Comparative examples 9 to 11 are shown in Table 4.
TABLE 4__________________________________________________________________________ White Resolution light sen- Spectral (line/mm) Initial Dark sitivity sensitiv- Charging.dis- TiOPc InPcCl charge dacay E.sub.1/2 ity E.sub.50 charging after (wt %) (wt %) V.sub.0 (-V) DDR (%) (lux .multidot. sec) (.mu.J/cm.sup.2) Initial 10.sup.4 times__________________________________________________________________________Example 13 75 25 820 66.9 0.7 0.31 12.5 12.5Example 14 90 10 850 56.8 1.0 0.42 12.5 12.5Example 15 25 75 700 38.1 1.7 0.93 10.0 10.0Example 16 50 50 700 42.3 1.2 0.67 12.5 10.0Comparative 100 0 980 44.2 1.3 0.72 10.0 6.3example 9Comparative 0 100 660 23.4 3.9 2.05 8.0 4.0example 10Comparative 75 25 290 5.2 -- -- 3.2 1.6example 11__________________________________________________________________________
Examples 17 to 20
Crystals and electrophotographic photoreceptors using the crystals were prepared according to Examples 1 to 4 except for using chloroaluminum phthalocyanine in place of chloroindium phthalocyanine used in Examples 1 to 4, and using 1 g of the above compound No. 4 in place of 1.5 g of the above compound No. 1 as a charge transport material.
Comparative Example 12
An electrophotographic photoreceptor was prepared according to Comparative example 1 except for using 1 g of the above charge transport substance No. 4 in place of 1.5 g of the above charge transport substance No. 1 used in Comparative example 1 as a charge transport material
Comparative Example 13
Crystal and an electrophotographic photoreceptor using the crystal were prepared according to Comparative example 2 except for using chloroaluminum phthalocyanine in place of chloroindium phthalocyanine used in Comparative example 2, and using 1 g of the above charge transport substance No. 4 in place of 1.5 g of the above charge transport substance No. 1 as a charge transport material.
Comparative Example 14
Powder was prepared according to Comparative example 3 except for using chloroaluminum phthalocyanine in place of chloroindium phthaiocyanine used in Comparative example 3, and an electrophotographic photoreceptor was prepared by using the powder. The X-ray diffraction spectrum of the powder was the same as that of FIG. 4.
The electrophotographic characteristics of Examples 17 to 20 and Comparative examples 12 to 14 are shown in Table 5.
TABLE 5__________________________________________________________________________ White Resolution light sen- Spectral (line/mm) Initial Dark sitivity sensitiv- Charging.dis- TiOPc InPcCl charge dacay E.sub.1/2 ity E.sub.50 charging after (wt %) (wt %) V.sub.0 (-V) DDR (%) (lux .multidot. sec) (.mu.J/cm.sup.2) Initial 10.sup.4 times__________________________________________________________________________Example 17 75 25 880 57.9 1.1 0.45 12.5 12.5Example 18 90 10 930 55.3 1.2 0.49 12.5 12.5Example 19 25 75 480 14.9 1.5 0.83 8.0 8.0Example 20 50 50 540 29.5 1.3 0.72 10.0 10.0Comparative 100 0 970 42.2 1.5 0.83 10.0 6.3example 12Comparative 0 100 420 9.7 2.6 1.38 6.3 3.2example 13Comparative 75 25 250 4.7 -- -- 3.2 1.6example 14__________________________________________________________________________
Examples 21 to 24
Crystals and electrophotographic photoreceptors using the crystals were prepared according to Examples 1 to 4 except for using 0.9 g of a polyvinyl butyral resin Ethlec BL-S (trade name, available from Sekisui Kagaku Co.) and 0.1 g of a melamine resin ML351W (trade name, available from Hitachi Chemical Co., Ltd.) in place of 1 g of a silicone resin KR-255 (trade name) used in Example 1, and using 49 g of 2-methoxyethanol and 49 g of tetrahydrofuran in place of 98 g of 1,2-dichloroethane used in Example 1.
Electrophotographic characteristics of Examples 21 to 24 are shown in Table 6.
In addition to the results shown in Table 6, samples of Examples 21 to 24 showed a low water absorbing ratio of the charge transport layer and no lowering in electrophotographic characteristics was observed even under high temperature and high humidity conditions.
TABLE 6__________________________________________________________________________ White Resolution light sen- Spectral (line/mm) Initial Dark sitivity sensitiv- Charging.dis- TiOPc InPcCl charge dacay E.sub.1/2 ity E.sub.50 charging after (wt %) (wt %) V.sub.0 (-V) DDR (%) (lux .multidot. sec) (.mu.J/cm.sup.2) Initial 10.sup.4 times__________________________________________________________________________Example 21 75 25 980 64.2 0.7 0.30 12.5 12.5Example 22 90 10 1010 64.3 0.7 0.31 12.5 12.5Example 23 25 75 840 42.8 1.2 0.65 12.5 10.0Example 24 50 50 850 42.2 1.0 0.55 12.5 10.0__________________________________________________________________________
Example 25
In 50 ml of sulfuric acid was dissolved 1 g of a phthalocyanine mixture comprising 0.75 g of titanylphthalocyanine and 0.25 g of chloroindium phthalocyanine, and the mixture was stirred at room temperature for 30 minutes. Subsequently, the mixture was added dropwise to one liter of a deionized water cooled with ice water over about 40 minutes to be reprecipitated. The mixture was further stirred for 1 hour under cooling, and left to stand overnight. After the supernatant was removed by decantation, the precipitates were separated by centrifugation to obtain 700 mg of the precipitates. In the first washing, to 700 mg of the precipitates was added 120 ml of a deionized water as a washing water, and the mixture was stirred. Then, the precipitates and the washing water were separated and removed by centrifugation. The same washing operation was carried out successively five Limes. The pH and conductivity of the washing water (namely washing water after washing) separated and removed in the sixth operation were measured (at 23.degree. C.) . The pH was measured by using Model PH51 (trade name, manufactured by Yokogawa Denki Co.). Further, the conductivity was measured by Model SC-17A (trade name, manufactured by Shibata Kagaku Kikai Kogyo Co.). The pH of the washing water was 3.3, and the conductivity was 65.1 .mu.S/cm. Subsequently, the precipitates were washed with 60 ml of methanol three times, and then dried under vacuum by heating at 60.degree. C. for 4 hours.
Next, 1 g of this product dried under vacuum was added to 10 ml of N-methyl-2-pyrrolidone, and the mixture was heated and stirred (150.degree. C., 1 hour). After filtration, the residue was washed with methanol and dried under vacuum by heating at 60.degree. C. for 4 hours to obtain crystal of the phthalocyanine composition of the present invention. The X-ray diffraction spectrum of this crystal is substantially the same as that in FIG. 1.
Examples 26 and 27
Phthalocyanine compositions were prepared in the same manner as in Example 25 except for changing washing times after treatment with sulfuric acid, The pH and conductivity of each washing water are shown in Table 7.
Comparative Examples 15 to 17
Phthalocyanine compositions were prepared in the same manner as in Example 25 except for changing washing times after treatment with sulfuric acid, The pH and conductivity of each washing water are shown in Table 7.
TABLE 7______________________________________ Washing times pH Conductivity (.mu.S/cm)______________________________________Comparative 3 0.7 15000example 15Example 25 6 3.3 262Example 26 9 3.8 36.0Example 27 12 4.0 17.8Comparative 18 4.5 5.8example 16Comparative 28 7.4 3.4example 17______________________________________
Examples 28 to 30
Crystals of phthalocyanine compositions were obtained according to Examples 25 to 27 except for using bromoindium phthalocyanine in place of chloroindium phthalocyanine used in Examples 25 to 27. The pH and conductivity of each washing water are shown in Table 8.
Comparative examples 18 to 20
Crystals of phthalocyanine compositions were obtained according to Comparative examples 15 to 17 except for using bromoindium phthalocyanine in place of chloroindium phthalocyanine used in Comparative examples 15 to 17. The pH and conductivity of each washing water are shown in Table 8.
TABLE 8______________________________________ Washing times pH Conductivity (.mu.S/cm)______________________________________Comparative 3 1.4 4500example 18Example 28 6 3.4 202Example 29 9 3.7 35.8Example 30 12 4.1 10.8Comparative 18 4.5 5.8example 19Comparative 28 7.7 3.1example 20______________________________________
Examples 31 to 33
Crystals of phthalocyanine compositions were obtained according to Examples 25 to 27 except for using chlorogallium phthalocyanine in place of chloroindium phthalocyanine used in Examples 25 to 27. The pH and conductivity of each washing water are shown in Table 9.
Comparative Examples 21 to 23
Crystals of phthalocyanine compositions were obtained according to Comparative examples 15 to 17 except for using chlorogallium phthalocyanine in place of chloroindium phthalocyanine used in Comparative examples 15 to 17. The pH and conductivity of each washing water are shown in Table 9.
TABLE 9______________________________________ Washing times pH Conductivity (.mu.S/cm)______________________________________Comparative 3 1.8 6800example 21Example 31 6 3.6 211Example 32 9 3.8 36.0Example 33 12 4.0 17.8Comparative 18 4.8 7.3example 22Comparative 28 7.1 3.4example 23______________________________________
Examples 34 to 36
Crystals of phthalocyanine compositions were obtained according to Examples 25 to 27 except for using chloroaluminum phthalocyanine in place of chloroindium phthalocyanine used in Examples 25 to 27. The pH and conductivity of each washing water are shown in Table 10.
Comparative examples 24 to 26
Crystals of phthalocvanine compositions were obtained according to Comparative examples 15 to 17 except for using chloroaluminum phthalocyanine in place of chloroindium phthalocyanine used in Comparative examples 15 to 17. The pH and conductivity of each washing water are shown in Table 10.
TABLE 10______________________________________ Washing times pH Conductivity (.mu.S/cm)______________________________________Comparative 3 1.1 7900example 24Example 34 6 3.2 234Example 35 9 4.0 20.3Example 36 12 4.4 12.8Comparative 18 5.3 5.5example 25Comparative 28 6.8 3.4example 26______________________________________
Example 37
1.5 g of the phthalocyanine composition prepared in Example 25, 1 g of a silicone resin KR-255 (trade name, produced by Shinetsu Kagaku Kogyo Co.) and 98 g of 1,2-dichloroethane were mixed, and the mixture was dispersed by a ball mill. The dispersion obtained was coated on an aluminum plate (conductive substrate, 100 mm.times.100 mm.times.0.1 mm) by the dip coating method, and dried at 140.degree. C. for 1 hour to form a charge generation layer having a thickness of 0.5 .mu.m.
A coating solution obtained by mixing 1.5 g of the above charge transport substance No. 4, 1.5 g of a polycarbonate resin Yupilon S-3000 (trade name, produced by Mitsubishi Gas Kagaku Co.) and 15.5 g of methylene chloride was coated on the above substrate by the dip coating method, and dried at 120.degree. C. for 1 hour to form a charge transport layer having a thickness of 20 .mu.m.
The electrophotographic characteristics of this electrophotographic photoreceptor were measured by an electrostatic copying paper testing device Model SP-428 (trade name, manufactured by Kawaguchi Denki Co.). The photoreceptor was charged by corona charging of -5 kV under dark condition, and initial charge Vo (-V) after 10 seconds, dark decay DDR (%) after 30 seconds and sensitivity E.sub.1/2 (lux.cndot.sec) when exposure was carried out by white light with a luminosity of 2 lux were determined.
As a result, it was found that V.sub.0 =640 (-V), DDR=68.5 (%) and E.sub.1/2 =0.7 (lux.cndot.sec).
Examples 38 and 39
Electrophotographic photoreceptors were prepared according to Example 37 except for using the titanylphthalocyanine compositions obtained in Examples 26 and 27, and evaluated. The results are shown in Table 11.
Comparative Examples 27 to 29
Electrophotographic photoreceptors were prepared according to Example 37 except for using the titanylphthalocyanine compositions obtained in Comparative examples 15 to 17, and evaluated. The results are shown in Table 11.
TABLE 11__________________________________________________________________________ Charge- Charge- Initial Dark Sensiti- generation transport charge decay vity E.sub.1/2 material material V.sub.0 (-V) DDR (%) (lux .multidot. sec)__________________________________________________________________________Example 37 Crystal obtained No. 4 640 68.5 0.7 in Example 25Example 38 Crystal obtained No. 4 780 51.3 0.6 in Example 26Example 39 Crystal obtained No. 4 670 50.7 0.7 in Example 27Comparative Crystal obtained No. 4 400 15.0 0.9example 27 in Comparative example 15Comparative Crystal obtained No. 4 390 19.2 0.9example 28 in Comparative example 16Comparative Crystal obtained No. 4 540 37.0 0.9example 29 in Comparative example 17__________________________________________________________________________
Examples 40 to 42
Electrophotographic photoreceptors were prepared according to Examples 37 to 39 except for using the titanylphthalocyanine compositions obtained in Examples 28 to 30 in place of that obtained in Example 37 and using Compound No. 2 in place of No. 4 as a charge transport material, and evaluated. The results are shown in Table 12.
Comparative Examples 30 to 32
Electrophotographic photoreceptors were prepared according to Example 37 except for using the titanylphthalocyanine compositions obtained in Comparative examples 18 to 20 and using Compound No. 2 in place of No. 4 as a charge transport material, and evaluated. The results are shown in Table 12.
TABLE 12__________________________________________________________________________ Charge- Charge- Initial Dark Sensiti- generation transport charge decay vity E.sub.1/2 material material V.sub.0 (-V) DDR (%) (lux .multidot. sec)__________________________________________________________________________Example 40 Crystal obtained No. 2 820 69.7 0.7 in Example 28Example 41 Crystal obtained No. 2 880 57.1 0.7 in Example 29Example 42 Crystal obtained No. 2 990 51.7 0.7 in Example 30Comparative Crystal obtained No. 2 410 25.9 1.1example 30 in Comparative example 18Comparative Crystal obtained No. 2 460 26.5 2.6example 31 in Comparative example 19Comparative Crystal obtained No. 2 500 30.1 2.0example 32 in Comparative example 20__________________________________________________________________________
Examples 43 to 45
Electrophotographic photoreceptors were prepared according to Examples 37 to 39 except for using the titanylphthalocyanine compositions obtained in Examples 31 to 33 in place of that obtained in Example 37 and using Compound No. 5 in place of No. 4 as a charge transport material, and evaluated. The results are shown in Table 13.
Comparative Examples 33 to 35
Electrophotographic photoreceptors were prepared according to Example 37 except for using the titanylphthalocyanine compositions obtained in Comparative examples 21 to 23 and using Compound No. 5 in place of No. 4 as a charge transport material, and evaluated. The results are shown in Table 13.
TABLE 13__________________________________________________________________________ Charge- Charge Initial Dark Sensiti- generation transport charge decay vity E.sub.1/2 material material V.sub.0 (-V) DDR (%) (lux .multidot. sec)__________________________________________________________________________Example 43 Crystal obtained No. 5 700 58.6 0.7 in Example 31Example 44 Crystal obtained No. 5 820 66.9 0.8 in Example 32Example 45 Crystal obtained No. 5 800 56.8 0.7 in Example 33Comparative Crystal obtained No. 5 520 24.2 1.3example 33 in Comparative example 21Comparative Crystal obtained No. 5 560 25.3 1.2example 34 in Comparative example 22Comparative Crystal obtained No. 5 600 36.3 1.5example 35 in Comparative example 23__________________________________________________________________________
Examples 46 to 48
Electrophotographic photoreceptors were prepared according to Examples 37 to 39 except for using the titanylphthalocyanine compositions obtained in Examples 34 to 36 in place of that obtained in Example 37 and using Compound No. 1 in place of No. 4 as a charge transport material, and evaluated. The results are shown in Table 14.
Comparative Examples 36 to 38
Electrophotographic photoreceptors were prepared according to Example 37 except for using the titanylphthalocyanine compositions obtained in Comparative examples 24 to 26 and using Compound No. 1 in place of No. 4 as a charge transport material, and evaluated. The results are shown in Table 14.
TABLE 14__________________________________________________________________________ Charge- Charge Initial Dark Sensiti- generation transport charge decay vity E.sub.1/2 material material V.sub.0 (-V) DDR (%) (lux .multidot. sec)__________________________________________________________________________Example 46 Crystal obtained No. 1 880 57.9 1.1 in Example 34Example 47 Crystal obtained No. 1 930 55.3 1.2 in Example 35Example 48 Crystal obtained No. 1 870 52.7 1.2 in Example 36Comparative Crystal obtained No. 1 420 23.7 2.6example 36 in Comparative example 24Comparative Crystal obtained No. 1 540 29.5 1.9example 37 in Comparative example 25Comparative Crystal obtained No. 1 480 30.7 2.0example 38 in Comparative example 26__________________________________________________________________________
An electrophotographic photoreceptor using a coating solution for a charge generation layer containing a novel phthalocyanine composition obtained by the preparation process of the present invention has excellent electrophotographic characteristics such as charging characteristics, dark decay, sensitivity and resolution power, and can be applied suitably to an electrophotographic process to which higher density and higher image quality than those of the prior art are required.

Number	Date	Country
4-025215	Feb 1992	JPX
4-097815	Apr 1992	JPX
4-266420	Jan 1992	JPX

Number	Name	Date
4728592	Ohaku et al.	Mar 1988
5059355	Ono et al.	Oct 1991
5183886	Takagishi	Feb 1993
5213929	Takano et al.	May 1993

Phthalocyanine composition, process for preparing the same and electrophotographic photoreceptor using the same

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