Electrophotographic photoconductor and a method for forming the same

BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to an electrophotographic photoconductor. In particular, it relates to an electrophotographic photoconductor comprising a conductive support, undercoating layer and photosensitive layer.
2. Description of the Related Art
An electrophotographic process using a photoconductor comprises the steps of placing the photoconductor in the dark and charging the surface thereof evenly by corona discharge, exposing a region to selectively discharge electric charges and form an electrostatic image in the nonexposed region, and subsequently depositing the colored charged particles (toner) to a latent image by electrostatic attraction and the like to visualizing it, thereby forming an image.
Primary characteristics required of photoconductors in the above serial process are as follows.
(1) It can be charged evenly to a suitable potential in a dark place.
(2) It has a high chargeability in a dark place and electric charges are less discharged.
(3) It has an excellent photosensitivity and discharges electric charges immediately by exposure.
Further, photoconductors needed to have stability and durability, for example, little residual potential because of easy discharge of the surface of the photoconductor; excellent mechanical strength and flexibility; stable electric properties with no change of chargeability, photosensitivity, residual potential and the like even after repeated use; and endurance against heat, light, temperature, humidity, ozone deterioration and the like.
Electrophotographic photoconductors are currently used for practical purposes. Such photoconductors are prone to generate carrier implantation from the surface of the conductive support, so that image defects are produced because of disappearance of or decrease in surface charges form a microscopic view. In order to solve the problem, and further to coat defects of the surface, to improve the charging properties and to improve adhesive and coating properties of the photosensitive layer, an undercoating layer is provided between the conductive support and photosensitive layer.
Conventional undercoating layers contain various type of resin materials and those containing titanium oxide powder or the like. Known materials for the undercoating layers formed of a single layer include resin materials such as polyethylene, polypropylene, polystyrene, acryl resins, vinyl chloride resins, vinyl acetate resins, polyurethane resins, epoxy resins, polyester resins, melamine resins, silicon resins, polyvinyl buthyral resins, polyamide resins; and copolymer having more than two repeating units of these resins; casein, gelatin, polyvinyl alcohol, ethyl cellulose and the like. Among them, polyamide resin is preferable (disclosed in Japanese Unexamined Patent Publication Sho 51 (1976)-114132 and Japanese Unexamined Patent Publication Sho 52 (1977)-25638). However, the electrophotographic photoconductors having a single layer formed of polyamide etc. as an undercoating layer have a defect of great residual potential storage, which reduces sensitivity and induces an overlap of an image. This tendency becomes conspicuous under a low humidity.
Therefore, for preventing the image defect and improving residual potential, Japanese Unexamined Patent Publication Sho 56 (1981)-52757 discloses an undercoating layer containing surface-untreated titanium oxide. In addition, Japanese Unexamined Patent Publication Sho 59 (1984)-93453 and Japanese Unexamined Patent Publication Hei 2 (1990)-81158 disclose an undercoating layer containing in the surface titanium oxide particles coated with alumina and the like for improving dispersion of the titanium oxide powder. Further, Japanese Unexamined Patent Publication Sho 63 (1988)-234261 and Japanese Unexamined Patent Publication Sho 63 (1988)-298251 propose an undercoating layer comprising titanium oxide particles and binder resin in which the mixing ratio of titanium oxide is optimized for prolongation of the life of photoconductors.
In the above described undercoating layer containing titanium oxide powder, titanium oxide having a grain-like shape has been used.
Coating methods used for forming the electrophotographic photoconductor include a spray method, bar coat method, roll coat method, blade method, ring method, dip coating method and the like. According to the dip coating method shown in FIG. 1, the electrophotographic photoconductor is formed by immersing a conductive support in a coating tank filled with a coating solution for the photosensitive layer and pulling up the immersed conductive support at a constant or changing speed. The dip coating method is often used for forming an electrophotographic photoconductor because it is relatively simple and excellent in productivity and cost.
Preferably, resins used for the undercoating layer are hardly soluble in a solvent of the coating solution for the photosensitive layer. Generally, either alcohol soluble or water soluble resin is used. The undercoating layer is formed by preparing an alcohol solution or dispersed solution of the resign as a coating solution for the undercoating layer and by coating the support with the coating solution for the undercoating solution.
When the undercoating layer comprises titanium oxide powder and binder resin in which the ratio of titanium oxide is small as compared with the binder resin, the volume resistance of the undercoating layer increases and carriers transportation generated by exposure are controlled or prevented. As a result, the residual potential raises, thereby forming an overlap in an image. Furthermore, when electrophotographic photoconductors are used repeatedly, they are significantly affected by the accumulation of residual potential, temperature and humidity. In particular, the accumulation of residual potential becomes conspicuous at a low humidity, thereby degrading stability and failing to provide sufficient properties of the phoroconductor.
With increase in the content of titanium oxide, these problems are solved. But, if the electrophotographic photoconductor is repeatedly used, the residual potential tends to be stored. Especially, the tenancy is significantly revealed at a low humidity, failing to completely solving the problem of the stability in a long duration and environmental properties.
Moreover, if the titanium oxide content increases to a ratio at which the content of the binder resin becomes virtually zero, the film strength of the undercoating layer decreases and adhesiveness between the undercoating layer and the conductive support is weakened with the result that after repeated use of the photoconductors the photosensitivity thereof is degraded due to the breakage of the film and the image is adversely affected. Additionally, photoconductors have a drawback of an abrupt decrease in volume resistance and low chargeability.
The titanium oxide powder used for the undercoating layer of the conventional invention has a particle size of 0.01 .mu.m or more and 1 .mu.m or less in the observation of the microscope, and the mean of the aspect ratio thereof is in the range of 1 or more to 1.3 or less. The particles have approximately spherical shape (hereinafter referred to "grain-like shape") despite some degree of unevenness. When the titanium oxide dispersed in the undercoating layer has the grain-like shape, the particles come into contact with each other at a point and the contact area thereof is small. Therefore, unless the content of the titanium oxide exceeds a certain level, the resistance of the undercoating layer is significantly high and the photoconductor properties, especially sensitivity and residual potential, are degraded. Accordingly, in case of titanium oxide of the grain-like shape, a larger content of titanium oxide is required in the undercoating layer.
Despite the improvement in the properties with the larger ratio of titanium oxide content, the photoconductor will never fail to be deteriorated through repeated use over a long time because of a weak contact between the particles.
When the content of titanium oxide is increased, the dispersion of titanium oxide to binder resin, in addition, dispersion and stability of the coating solution for the undercoating layer are deteriorated. This produces coating unevenness when the undercoating layer is applied in the process of forming the photoconductor, thereby failing to provide excellent image properties. Therefore, a coating solution for the undercoating layer which satisfies a sufficient dispersion and stability has been demanded.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic view showing an example of a dip coating device used for forming an electrophotographic photoconductor.
FIG. 2 is a sectional view of an electrophotographic photoconductor having a function separated structure formed in an Example of the present invention.

SUMMARY OF THE INVENTION
The present invention provides an electrophotographic photoconductor comprising a conductive support, an undercoating layer provided on the conductive support and a photosensitive layer provided on the undercoating layer, in which the undercoating layer comprises needle-like titanium oxide particles and a binder resin. The needle-like titanium oxide particles in the undercoating layer show a volume resistance in the range from 10.sup.5 .OMEGA..multidot.cm to 10.sup.10 .OMEGA..multidot.cm when a loading pressure of 100 Kg/cm.sup.2 is applied.
The present invention further provides a method for forming the electrophotographic photoconductor, in which the undercoating layer is formed by using a coating solution comprising the needle-like titanium oxide particles, the binder resin and an organic solvent, the binder resin is a polyamide resin and the organic solvent is a mixture of an azeotropic mixture of C.sub.1-3 lower alcohol and another organic solvent selected from the group consisting of dichloromethane, chloroform, 1,2-dichloroethane, 1,2-dichloropropane, toluene and tetrahydrofuran.
The azeotropic mixture mentioned above is a mixture solution in which a composition of the liquid phase and a composition of the vapor phase are coincided with each other at a certain pressure to give a mixture having a constant boiling point. The composition is determined by a combination of C.sub.1-3 lower alcohol and another organic solvent selected from the group consisting of dichloromethane, chloroform, 1,2-dichloroethane, 1,2-dichloropropane, toluene and tetrahydrofuran, which is known by the person skilled in the art. For example, a mixture consisted of 35 parts by weight of methanol and 65 parts by weight of 1,2-dichloroethane is azeotropic solution. The azeotropic composition leads a uniform evaporation, thereby forming an even undercoating layer without coating defects and improving a storage stability of the coating solution for the undercoating layer.
An object of the present invention is to provide an electrophotographic photoconductor having favorable properties such as good chargeability and low residual potential, and being excellent in stability after repeatedly used and in environmental properties such that only a few amount of residual potential is accumulated and the photosensitivity is not degraded after repeated use.
Another object of the present invention is to provide an electrophotographic photoconductor in which the surface of the undercoating layer is so flat that photosensitive layer can be applied evenly, thereby substantially overcoming the defects of the conductive support.
Still another object of the present invention is to provide a method for forming the electrophotographic photoconductor in which the photosensitive layer is evenly coated and which provides an excellent image properties.
Yet another object of the present invention is to provide the coating solution for the undercoating layer having an excellent storage stability which is capable of forming even coating film without aggregation for a long duration.
DESCRIPTION OF PREFERRED EMBODIMENT
Titanium oxide particles used for the undercoating layer of the present invention have a needle-like shape. The term "needle-like" means a long and narrow shape including a stick and pole and it is a shape having an aspect ratio L/S of a length L of the long axis to a length S of the short axis of 1.5 or more. It is not necessary to be extremely long and narrow or have a sharp pointed end. The mean of the aspect ratio is preferably in the range from 1.5 to 300, more preferably from 2 to 10. The short axis and long axis of the particle diameter of the needle-like titanium oxide are 1 .mu.m or less and 100 .mu.m or less, respectively, more preferably, 0.5 .mu.m or less and 10 .mu.m or less, respectively.
Such methods as natural sedimentation method and photo-extinction method and the like may be used for measuring the diameter and aspect ratio. As the titanium oxide particles have a needle-like shape, microscopic observation may be preferably used for measuring the diameter and aspect ratio thereof. The undercoating layer contains the titanium oxide and binder resin. The content of the needle-like titanium oxide particles is in the range from 10 wt % to 99 wt %, preferably from 30 wt % to 99 wt %, most preferably 50 wt % to 95 wt %. In the present invention, the needle-like titanium oxide particles may be used together with titanium oxide having a grain-like shape.
Titanium oxide has two crystal forms including anatase and rutile, both of which can be used for the present invention singly or in combination.
The needle-like titanium oxide fine particles are required to have a volume resistance as high as a level in the range from 10.sup.5 .OMEGA..multidot.cm to 10.sup.10 .OMEGA..multidot.cm under a loading pressure of 100 Kg/cm.sup.2. Hereinafter, the volume resistance provided when the loading pressure of 100 Kg/cm.sup.2 is applied is referred to simply as a powder resistance.
When the powder resistance of the needle-like titanium oxide particles is less than 10.sup.5 .OMEGA..multidot.cm, the resistance of the undercoating layer lowers and does not work as a charge blocking layer.
For example, when is treated with a conductive treatment by using an SnO.sub.2 conductive layer doped with antimony, titanium oxide shows a very low powder resistance such as 10.sup.0 .OMEGA..multidot.cm or 10.sup.1 .OMEGA..multidot.cm. In that case, the titanium oxide can not be used as the undercoating layer because it can not work as an electric charge blocking layer and chargeability of the photoconductor is degraded. On the other hand, if the powder resistance of the titanium oxide becomes high as 10.sup.10 .OMEGA..multidot.cm or more to reach the same level as the volume resistance of the binder resin or more, transportation of carriers generated by exposure is controlled or prevented. This leads to an increase in residual potential, so that it is not preferred.
Besides, as long as the powder resistance of the needle-like titanium oxide particles remain within the above scope, the surface of the titanium oxide particles may remain untreated or may be coated with Al.sub.2 O.sub.3, SiO.sub.2, ZnO and the like or the mixture thereof for improvement in dispersion properties and surface smoothness.
The binder resin contained in the undercoating layer may be formed of the same materials as that of the undercoating layer formed as a single resin layer. Among them, polyamide resin is preferably used because it satisfies various conditions required of the binder resin such as (i) polyamide resin is neither dissolved nor swollen in a solution used for forming the photosensitive layer on the undercoating layer, and (ii) polyamide resin has an excellent adhesiveness with a conductive support as well as flexibility. In the polyamide resin, alcohol soluble nylon resin is most preferable, for example, copolymer nylon polymerized with 6-nylon, 6,6-nylon, 610-nylon, 11-nylon, 12-nylon and the like; and nylon which is chemically denatured such as N-alkoxy methyl denatured nylon and N-alkoxy ethyl denatured nylon.
The undercoating layer is formed by preparing a mixture solvent comprising the lower alcohol and the organic solvent described above which preferably is an azeotropic solvent; dispersing the polyamide resin and titanium oxide particles in the mixture solvent to form a coating solution for the undercoating layer; coating the conductive support with the coating solution and drying it. The organic solvent is combined for improving dispersion in the alcohol solvent and preventing the coating solution from gelation with the elapse of time. Further, the azeotropic solvent is used for preventing the composition of the coating solution from being changed as the time passes, whereby storage stability of the coating solution can be improved and the coating solution can be reproduced. The storage is represented by the number of dates counted from the date of forming the coating solution for the undercoating layer (hereinafter referred to a pot life).
The thickness of the undercoating layer is preferably in the range from 0.01 .mu.m to 10 .mu.m, more preferably from 0.05 .mu.m to 5 .mu.m.
The coating solution for the undercoating layer is dispersed by using a ball mill, sand mill, attritor, oscillating mill or ultrasonic mill etc. and is coated by a general method such as dip coating method as described above.
The conductive support used for the present invention includes a metal drum or sheet formed of aluminium, aluminium alloy, copper, zinc, stainless steel, nickel or titanium etc.; and a drum, sheet or seamless belt formed by treating the surface of a polymer material such as polyethylene terephthalate, nylon, polystyrene and the like or a hard paper laminated with metal leaf or metallizing.
The photosensitive layer formed on the undercoating layer may have a function separated structure comprising electric charge generation layer and electric charge transport layer in which function is separated or a single layer structure.
In case of function separated photoconductors, the electric charge generation layer is firstly formed on the undercoating layer. The electric charge generating substance contained in the electric charge generation layer includes bis-azo compounds such as chlorodiane blue, polycyclic quinone compounds such as dibromoanthanthrone, perylene compounds, quinacridone compounds, phthalocyanine compounds and azulenium salts, which may be used solely or in combination. The electric charge generation layer can be formed by directly forming the compound under vacuum evaporation. Alternatively, it can be formed by dispersing the charge generating substance into the binder resin solution. As a method for forming the electric charge generation layer, the latter is generally preferable. In the latter process, the steps for mixing or dispersing the electric charge generating substances into the binder resin solution and coating are the same as that of the undercoating layer. The binder resin of the present invention may be a conventional resin which is used solely or in combination. Preferably, melamine resins, epoxy resins, silicon resins, polyurethane resins, acryl resins, polycarbonate resins, polyarylate resins, phenoxy resins, and copolymer resins formed of two or more repeating units described above are used. As the copolymer, an insulating resin such as vinyl chloride-vinyl acetate copolymer resin, acrylonitrile-styrene copolymer may be used.
The solvent used for dissolving these resins includes haligenated hydrocarbons such as methylene chloride and dichloroethane; ketones such as acetone, methylethylketone and cyclohexanone; esters such as ethyl acetate and butyl acetate; ethers such as tetrahydrofuran and dioxane; aromatic hydrocarbons such as benzene, toluene and xylene; nonprotonic polar solvents such as N,N-dimethylformamide, N,N-dimethylacetamide and dimethylformamide. The thickness of the electric charge generation layer is preferably in the range from 0.05 .mu.m to 5 .mu.m, more preferably from 0.1 .mu.m to 1 .mu.m.
The electric charge transporting substances contained in the electric charge transport layer formed on the electric charge generation layer includes hydrazone compounds, pyrazoline compounds, triphenylamine compounds, triphenylmethane compounds, stilbene compounds, oxadiazole compounds and the like. The coating solution for the electric charge transport layer is formed by dissolving the electric charge transporting substances into the binder resin solution.
The coating step of the electric charge transporting substance is the same method as that of the undercoating layer. The thickness of the electric charge transport layer is preferably in the range from 5 .mu.m to 50 .mu.m, more preferably from 10 .mu.m to 40 .mu.m.
When the photosensitive layer is formed of a single structure, the thickness of the photosensitive layer is preferably in the range from 5 .mu.m to 50 .mu.m, more preferably from 10 .mu.m to 40 .mu.m.
Since the undercoating layer works as a barrier against implantation of carrier from the conductive support and has a high sensitivity and durability irrespective of the structural type, negative photosensitive layer is preferable.
For the purpose of improving the sensitivity, lowering the residual potential and preventing fatigue after repeated use, at least one type of electron acceptor can be added to the photoconductor. Examples of the electron acceptor include quinone compounds such as para-benzoquinone, chloranil, tetrachloro 1,2-benzoquinone, hydroquinone, 2,6-dimehylbenzoquinone, methyl 1,4-benzoquinone, .alpha.-naphthoquinone and .beta.-naphthoquinone; nitro compounds such as 2,4,7-trinitro-9-fluorenone, 1,3,6,8-tetranitrocarbazole, p-nitro benzophenone, 2,4,5,7-tetranitro-9-fluorenone and 2-nitrofluorenone; and cyano compounds such as tetracyanoethylene, 7,7,8,8-tetracyanoquinodimethane, 4-(p-nitrobenzoyloxy)-2',2'-dicyanovinylbenzene, 4-(m-nitrobenzoyloxy)-2',2'-dicyanovinylbenzene. Among them, fluorenone compounds, quinone compounds and benzene derivatives containing an electron-withdrawing substituent such Cl, CN and NO.sub.2 are most preferable. The photosensitive layer may further contain an UV absorber or antioxidant such as benzoic acid, stilbene compounds and derivatives thereof and nitrogen containing compounds such as triazole compounds, imidazole compounds, oxadiazole compounds, thiazole compounds and derivatives thereof.
Further, if necessary, a protective layer may be formed on the photosensitive layer to protect the surface. As the protective layer, thermoplastic resin, photosetting or thermosetting resin may be used. The protective layer may contain the UV absorber or antioxidant; inorganic material such as metal oxide; organic metal compound; electron acceptor substance and the like. In addition, plasticizer such as dibasic ester, fatty acid ester, phosphoric ester, phthalic acid ester and chlorinated paraffin may be added to add processing ability and plasticity and to improve the physical properties, if it is necessary. Further, a levelling agent such as silicon resin may be used.
Since the particle of the needle-like titanium oxide has a long and narrow shape, the particles are easily in contact with each other and the contact area between the particles is greater than that of the grain-like particles. Therefore, even if the content of the titanium oxide in the undercoating layer is smaller than the grain-like particles, the undercoating layer having an equivalent properties can be easily produced. Employing a reduced amount of titanium oxide is advantageous for improving the film strength and adhesive properties with the conductive support. The properties of the photoconductor containing the needle-like titanium oxide particles are not degraded after repeated use because the contact between the particles thereof are strong, whereby excellent stability is obtained.
When two undercoating layers are provided one of which contains the needle-like titanium oxide particles and the other contains the grain-like titanium oxide particles with the same content, the undercoating layer containing the needle-like titanium oxide particles have smaller resistance than the undercoating layer containing the grain-like titanium oxide particles is smaller than that of the grain-like titanium oxide particles. This allows forming the undercoating layer containing the needle-like titanium oxide particles thicker than that of containing the grain-like one. As a result, the surface defect of the conductive support hardly appears on the surface of the undercoating layer containing the needle-like titanium oxide, which means the needle-like titanium oxide is favorable in obtaining a smooth surface of the undercoating layer.
Additionally, the undercoating layer containing the needle-like particles, even without any particular surface treatment, exhibit a very stable dispersion properties with respect to a mixed solvent of a lower alcohol used for coating solution for the undercoating layer and other organic solvents or a mixed solvent comprising an azeotropic composition thereof, so that the stability can be maintained over a long period and the surface of the support can be coated evenly. As a result, a uniform and favorable image properties can be obtained.
Examples
The present invention will be detailed in accordance with drawings illustrating examples, but it is not limited to them. In the examples is employed a function-separated type electrophotographic photoconductor. However, the similar effects can be obtained using a single-layer structure electrophotographic photoconductor.
EXAMPLES 1 to 5
FIG. 2 is a sectional view schematically illustrating a function-separated type electrophotographic photoconductor of Examples in accordance with the present invention. The electrophotographic photoconductor comprises an undercoating layer 2 formed on a conductive support 1 and a photosensitive layer 5 formed on the undercoating layer. The photosensitive layer comprises an electric charge generation layer 3 containing an electric charge generation substance 30 and an electric charge transport layer 4 containing an electric charge transport substance 40.
To a mixed solvent comprising 28.7 parts by weight of methyl alcohol and 53.3 parts by weight of 1,2-dichloroethane were mixed 1.8 parts by weight of STR-60N (manufactured by Sakai Chemical Industry Co., Ltd.) not applied with surface treatment and having a powder resistance of about 9.times.10.sup.5 .OMEGA..multidot.cm, length of longitudinal axis L=0.05 .mu.m, length of short axis S=0.01 .mu.m and aspect ratio 5, as needle-like titanium oxide, and 16.2 parts by weight of copolymer nylon resin (manufactured by Toray Industries, Inc.: CM8000) as binder resin. The mixture was dispersed for 8 hours by a paint shaker to form a coating solution for the undercoating layer. The coating solution thus formed was coated on an aluminum-made conductive support having a thickness of 100 .mu.m as a conductive support 1 with a baker applicator, followed by drying the coated support with hot air for 10 minutes at 110.degree. C. to provide the undercoating layer 2 having a dried thickness of 3.0 .mu.m. When the coating solution is dried, the solvent is evaporated and the needle-like titanium oxide and the copolymer nylon resin are left as the undercoating layer to set the content of the needle-like titanium oxide 10 wt %.
In addition, 1.5 parts by weight of a bis-azo pigment (chlorodiane blue) having the following chemical formula 1 and 1.5 parts by weight of phenoxy resin (manufactured by Union Carbide: PKHH) were mixed to 97 parts by weight of 1,2-dimethoxyethane, followed by being dispersed for 8 hours with the paint shaker to form the coating solution for electric charge generation layer. This coating solution for the electric charge generation layer was coated on the undercoating layer 2 with the baker applicator. Then, the coating solution was dried with hot air for 10 minutes at a 90.degree. C. to provide the electric charge generation layer 3 having a dried thickness of 0.8 .mu.m.
Further, 1 part by weight of a hydrazone compound of the chemical formula 2, 0.5 part by weight of a polycarbonate resin (manufactured by Mitsubishi Gas Chemical Company, Ltd.: Z-200) and 0.5 parts by weight of polyarylate resin (manufactured by Unichika: U-100) were mixed to 8 parts by weight of dichloromethane, followed by stirring and dissolving the mixture with a magnetic stirrer to form a coating solution for the electric charge transport layer. This coating solution for the electric charge transport layer was coated on the electric charge generation layer 3 with a baker applicator. This coating solution was dried with hot air for 1 hour at 80.degree. C. to provide the electric charge transport layer 4 having a dried thickness of 20 .mu.m, thereby forming a function-separated type electrophotographic photoconductor shown in FIG. 2. ##STR1##
Thus the electrophotographic photoconductor was loaded on an actual device (manufactured by Sharp Kabushiki Kaisha: SF-8870) to measure a surface potential of the photoconductor at a developing section, for example, a surface potential of the photoconductor (V.sub.O) in darkness except for the exposing process to examine the charging capabilities, the surface potential after discharge (V.sub.R) and a surface potential of the photoconductor (V.sub.L) at a blank portion when exposed to examine sensitivity. These photoconductive properties were measured at the initial point and after 20000 times repetitive use in the following conditions: low temperature/low humidity of 5.degree. C./20% RH (hereinafter abbreviated as "L/L"), normal temperature/normal humidity of 25.degree. C./60% RH (hereinafter abbreviated as "N/N") and high temperature/high humidity of 35.degree. C./85% RH (hereinafter abbreviated as "H/H"). Example 1 of Table 1 shows the results of the measurements.
Examples 2 to 5 of the electrophotographic photoconductor were formed in the same manner as Example 1 except that the mixing rate of the needle-like titanium oxide and the copolymer nylon resin was varied so that the content of the titanium oxide was 50, 80, 95 and 99 wt % to provide an undercoating layer, thereby measuring the photoconductive properties. The results of the measurements are shown in Examples 2 to 5 of Table 1 in the same manner.
EXAMPLES 6 TO 10
Examples 6 to 10 of the electrophotographic photoconductor were formed using the same STR-60N (manufactured by Sakai Chemical Industry Co., Ltd.) as Examples 1 to 5, using N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.) as binder resin in an undercoating layer and by varying the mixing rate of N-methoxymethyl nylon resin in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 1 shows the results of the measurements.
The results shown in Table 1 allow providing a photoconductor favorable in photoconductive properties within the scope of 10 to 99 wt % of the content of the needle-like titanium oxide to which surface treatment is not applied and having an aspect ratio of 5, and excellent in repetitive stability in each environment.
EXAMPLES 11 TO 15
Examples 11 to 15 of the electrophotographic photoconductor were formed using FTL-100 (manufactured by Ishihara Sangyo Kaisha, Ltd.), as needle-like titanium oxide, to which surface treatment is not applied and having a powder resistance of about 3.times.10.sup.5 .OMEGA..multidot.cm, L=3 to 6 .mu.m, S=0.05 to 0.1 .mu.m and an aspect ratio of 30 to 120, using copolymer nylon resin (manufactured by Toray Industries, Inc.: CM8000) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 2 shows the results of the measurements.
EXAMPLES 16 TO 20
Examples 16 to 20 of the electrophotographic photoconductor were formed using the same FTL-100 (manufactured by Ishihara Sangyo Kaisha, Ltd.) as Examples 11 to 15, using N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 2 shows the results of the measurements.
The results shown in Table 2 allow providing a photoconductor favorable in photoconductive properties within the scope of 10 to 99 wt % of the content of the needle-like titanium oxide to which surface treatment is not applied and having an aspect ratio of 30 to 120, and excellent in repetitive stability in each environment.
EXAMPLES 21 TO 25
Examples 21 to 25 of the electrophotographic photoconductor were formed using STR-60 (manufactured by Sakai Chemical Industry Co., Ltd.), as needle-like titanium oxide, coated with Al.sub.2 O.sub.3 and having a powder resistance of about 4.times.10.sup.6 .OMEGA..multidot.cm, L=0.05 .mu.m, S=0.01 .mu.m and an aspect ratio of 5, using copolymer nylon resin (manufactured by Toray Industries, Inc.: CM8000) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 3 shows the results of the measurements.
EXAMPLES 26 TO 30
Examples 26 to 30 of the electrophotographic photoconductor were formed using the same STR-60 (manufactured by Sakai Chemical Industry Co., Ltd.) as Examples 21 to 25, as needle-like titanium oxide, using N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 3 shows the results of the measurements.
The results shown in Table 3 allow providing a photoconductor favorable in photoconductive properties within the scope of 10 to 99 wt % of the content of the needle-like titanium oxide coated with Al.sub.2 O.sub.3 and having an aspect ratio of 5, and excellent in repetitive stability in each environment.
Comparative Examples 1 to 5
Comparative Examples 1 to 5 of the electrophotographic photoconductor were formed using TTO-55N (manufactured by Ishihara Sangyo Kaisha, Ltd.), as grain-like titanium oxide, to which surface treatment is not applied and having a powder resistance of about 5.times.10.sup.5 .OMEGA..multidot.cm and an average particle diameter of 0.03 .mu.m, using copolymer nylon resin (manufactured by Toray Industries, Inc.: CM8000) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 4 shows the results of the measurements.
Comparative Examples 6 to 10
Comparative Examples 6 to 10 of the electrophotographic photoconductor were formed using the same TTO-55N (manufactured by Ishihara Sangyo Kaisha, Ltd.) as Comparative Examples 1 to 5, as grain-like titanium oxide, using N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 4 shows the results of the measurements.
The results shown in Table 4 indicate that in use of grain-like titanium oxide to which surface treatment is not applied, residual potential V.sub.R is stored in large quantity and sensitivity V.sub.L is greatly degrated after 20000 times repetitive use when the content of the titanium oxide is 10 and 50 wt %. With the increase of the content of the titianium oxide, deterioration of the photoconductive properties is improved. When the content is 95 and 99 wt %, the electrophotographic photoconductor exhibits relatively favorable photoconductive properties in the environmental conditions of N/N and H/H. However, after 20000 times repetitive use in the environmental condition of L/L, the residual potential V.sub.R is stored in large quantity and the sensitivity V.sub.L is degraded. Comparative Examples 11 to 15
Comparative Examples 11 to 15 of the electrophotographic photoconductors were formed using TTO-55A (manufactured by Ishihara Sangyo Kaisha, Ltd.), as grain-like titanium oxide, coated with Al.sub.2 O.sub.3 and having a powder resistance of about 4.times.10.sup.7 .OMEGA..multidot.cm and an average particle diameter of 0.03 .mu.m, using copolymer nylon resin (manufactured by Toray. Industries, Inc.: CM8000) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 5 shows the results of the measurements.
Comparative Examples 16 to 20
Comparative Examples 16 to 20 of the electrophotographic photoconductor were formed using the same TTO-55A (manufactured by Ishihara Sangyo Kaisha, Ltd.) as Comparative Examples 11 to 15, as grain-like titanium oxide, using N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 5 shows the results of the measurements.
The results shown in Table 5 indicate that in use of non-conductive, grain-like titanium oxide coated with Al.sub.2 O.sub.3, the residual potential V.sub.R is stored in large quantity and the sensitivity V.sub.L is greatly degraded after 20000 times repetitive use when the content of the titanium oxide is 10 and 50 wt %. With the increase of the content of the titanium oxide, deterioration of the photoconductive properties is improved. When the content is 95 and 99 wt %, the electrophotographic photoconductor exhibits relatively favorable photoconductive properties in the environmental conditions of N/N and H/H. However, after 20000 times repetitive use in the environmental condition of L/L, the residual potential V.sub.R is stored in large quantity and the sensitivity V.sub.L is degraded.
Comparative Examples 21 to 25
Comparative Examples 21 to 25 of the electrophotographic photoconductor were formed using FTL-1000 (manufactured by Ishihara Sangyo Kaisha, Ltd.), as needle-like titanium oxide, of which surface is rendered to be conductive by being treated with SnO.sub.2 (doped with antimony) and having a powder resistance of about 1.times.10.sup.1 .OMEGA..multidot.cm, L=3 to 6 .mu.m, S=0.05 to 0.1 .mu.m and an aspect ratio of 30 to 120, using copolymer nylon resin (manufactured by Toray Industries, Inc.: CM8000) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 6 shows the results of the measurements.
Comparative Examples 26 to 30
Comparative Examples 26 to 30 of the electrophotographic photoconductor were formed using the same FTL-1000 (manufactured by Ishihara Sangyo Kaisha, Ltd.) as Comparative Examples 21 to 25, as needle-like titanium oxide, using N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) as binder resin in an undercoating layer and by varying the mixing rate in the same manner as Examples 1 to 5 to provide the undercoating layer, thereby measuring the photoconductive properties. Table 6 shows the results of the measurements.
The results shown in Table 6 indicate that in use of needle-like titanium oxide applied with conductive threatment, with the increase of the content of the titanium oxide, charging properties V.sub.O is degraded and further, after 20000 times repetitive use, extremely deteriorated to the level that the electrophotographic photoconductor is hardly charged.
EXAMPLE 31
Example 31 of the function-separated electrophotographic photoconductor was formed in the same manner as in Example 1 except that with a dip coating device as shown in FIG. 1, a coating solution for an undercoating layer having a dried thickness of 3.0 .mu.m, prepared using 17.1 parts by weight of needle-like titanium oxide and 0.9 parts by weight of copolymer nylon resin as binder resin was dip coated on an aluminum-made drum-like conductive support having a size of 1 mm(t).times.80 mm(.phi.).times.348 mm and a maximum surface roughness of 0.5 .mu.m, which was then dip coated with a coating solution for an electric charge generation layer and that for electric charge transport layer. The conductive support thus coated was loaded on an actual device (manufactured by Sharp Kabushiki Kaisha: SF-8870) to perform an image evaluation. Table 7 shows the result of the evaluation.
EXAMPLES 32 TO 35
Examples 32 to 35 of the electrophotographic photoconductor were formed in the same manner as in Example 31 except that 1,2-dichloroethane which is the organic solvent of the coating solution for the undercoating layer of Example 31 was replaced with 1,2-dichloropropane, chloroform, tetrahydrofuran and toluene respectively to make an azetropic composition having the mixing rate with methyl alcohol as shown in Table 7 to perform the image evaluation in the same manner as Example 31. Table 7 shows the result of the evaluation.
EXAMPLES 36 TO 40
Examples 36 to 40 of the electrophotographic photoconductors were formed in the same manner as in Examples 31 to 35 except that with the coating solution for the undercoating layer of Examples 31 to 35 the rate of the methyl alcohol and each organic solvent was set to 41:41 to perform the image evaluation in the same manner as Example 31. Table 7 shows the result of the evaluation.
Comparative Example 31
Comparative Example 31 of the electrophotographic photoconductor was formed in the same manner as Example 31 except that methyl alcohol of 82 parts by weight was singly used for the solvent of the coating solution for the undercoating layer of Example 31 to perform the image evaluation in the same manner as Example 31. Table 7 shows the result of the evaluation.
EXAMPLES 41 TO 50
Examples 41 to 50 of the electrophotographic photoconductors were formed in the same manner as Examples 31 to 40 except that the pot life in the coating solution for the undercoating layer has passed 30 days to perform the image evaluation. Table 8 shows the result of the evaluation.
Comparative Example 32
Comparative Example 32 of the electrophotographic photoconductors was formed in the same manner as Examples 31 except that the pot life in the coating solution for the undercoating layer has passed 30 days to perform the image evaluation. Table 8 shows the result of the evaluation.
EXAMPLE 51
The turbidity of the coating solution for the undercoating layer of Example 31 was measured using a turbidimeter with integrating sphere (manufactured by Mitsubishi Chemical Industries Ltd.: SEPPT-501D) to perform the evaluation in dispersibility and stability. Table 9 shows the result of the evaluation.
EXAMPLE 52
The turbidity of the coating solution for the undercoating layer used in Example 51 was measured after the pot life has passed 30 days, thereby performing the evaluation in dispersibility and stability. Table 9 shows the result of the evaluation.
EXAMPLE 53
A coating solution for the undercoating layer was formed in the same manner as Example 31 except that the solvent comprised 41 parts by weight of the ethyl alcohol and 41 parts of weight of 1,2-dichloropropane to measure the turbidity in the same manner as Example 51 to perform the evaluation in dispersibility and stability. Table 9 shows the result of the evaluation.
Example 54
The turbidity of the coating solution for the undercoating layer used in Example 53 was measured in the same manner as Example 51 except that the pot life has passed 30 days to perform the evaluation in dispersibility and stability. Table 9 shows the result of the evaluation.
Comparative Example 33
The turbidity of the coating solution for the undercoating layer of Comparative Example 31 was measured in the same manner as Example 51 to perform the evaluation in dispersibility and stability. Table 9 shows the result of the evaluation.
Comparative Example 34
The turbidity of the coating solution for the undercoating layer used in Comparative Example 32 in which the pot life has passed 30 days was measured in the same manner as Example 51 to perform the evaluation in dispersibility and stability. Table 9 shows the result of the evaluation.
Comparative Example 35
The surface-untreated, needle-like titanium oxide used for the coating solution for the undercoating layer of Example 31 was replaced with grain-like titanium oxide (manufactured by Ishihara Sangyo Kaisha, Ltd.: TTO-55N) not applied with surface treatment and having a powder resistance of 10.sup.7 .OMEGA..multidot.cm and an average particle diameter of 0.03 .mu.m. Then the turbidity was measured in the same manner as Example 51 to perform the evaluation in dispersibility and stability. Table 9 shows the result of the evaluation.
In view of the results of Examples 31 to 54, using the surface-untreated, needle-like titanium oxide and the mixed solvent in accordance with the present invention as a solvent allowed improving the dispersibility and the stability of the coating solution.
EXAMPLES 55 TO 56
Examples 55 to 56 of the electrophotographic photoconductor having an undercoating layer with a dried thickness of 1.0 .mu.m were formed in the same manner as Examples 31 and 32 except that the coating solution for the undercoating layer was dip coated on an aluminum-made drum-like conductive support which is the same as that of Examples 31 and 32 except for having a maximum surface roughness of 0.2 .mu.m to perform the image evaluation in the environmental conditions of L/L of 5.degree. C./20% RH, N/N of 25.degree. C./60% RH, H/H of 35.degree. C./85% RH respectively at the initial point and after 20000 times repetitive use in the same manner as Example 31.
The results of Examples 55 and 56 allowed providing the excellent quality of the image free from image irregularities resulted from defects and coating irregularities caused in the conductive support in all environmental conditions. Besides, the quality of the image after 20000 times repetitive use was equally favorable to that at the initial point.
EXAMPLES 57 AND 58
Examples 57 and 58 of the electrophotographic photoconductor were formed in the same manner as Example 55 except that binder resin of the coating solution for the undercoating layer of Examples 31 and 32 was replaced with N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) to perform the image evaluation.
The results of Examples 57 and 58 allowed providing the excellent quality of the image free from image irregularities in all environmental conditions. Besides, the quality of the image after 20000 times repetitive use was equally favorable to that at the initial point.
Comparative Example 36
Comparative Example 36 of the electrophotographic photoconductor was formed in the same manner as Example 55 except that binder resin of the coating solution for the undercoating layer of Example 31 was replaced with butyral resin (manufactured by Denki Kagaku Kogyo Kabushiki Kaisha: 3000K) which is not copolymer nylon resin to perform the image evaluation.
The results of Comparative Example 36 indicated that the undercoating layer was dissolved in a solvent for an electric charge generation layer when the electric charge generation layer was dip coated to cause liquid lopping and irregularities in a coating film of the electric charge generation layer. Further image irregularities resulted from these coating irregularities were caused. In particular, the image irregularities were outstandingly exhibited after 20000 repetitive.
Comparative Example 37
Comparative Example 37 of the electrophotographic photoconductor was formed in the same manner as Example 55 except for using, as needle-like titanium oxide, FTL-1000 (manufactured by Ishihara Sangyo Kaisha, Ltd.), of which surface is rendered to be conductive by being treated with SnO.sub.2 (doped with antimony), and having a powder resistance of 1.times.10.sup.1 .OMEGA..multidot.cm, L=3 to 6 .mu.m, S=0.05 to 0.1 .mu.m and an aspect ratio of 30 to 120 to perform the image evaluation.
The results of Comparative Example 37 indicated very poor charging properties and extremely degraded image tone in a solid black portion. In particular, the conspicuous eduction was caused after 20000 repetitive.
Comparative Example 38
Comparative Example 38 of the electrophotographic photoconductor was formed in the same manner as Example 55 except that titanium oxide used in the undercoating layer of Example 55 was removed and that the content of copolymer nylon resin was 18 parts by weight to perform the image evaluation.
The results of Comparative Example 38 indicated very high residual potential, extremely degraded sensitivity and an overlap of image in a white portion. In particular, the overlap of image was outstandingly caused in low temperature and low moisture conditions merely after 1000 times repetitive use.
As apparent from the above results, the dispersibility and stability of the coating solution can be improved by using a mixed solvent in accordance with the present invention as a solvent for the coating solution for the undercoating layer and the needle-like titanium oxide, thereby providing an electrophotographic photoconductor having favorable image properties free from coating irregularities.
EXAMPLES 59 TO 61
Example 59 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 31 except that the needle-like titanium oxide and binder resin in the coating solution for the undercoating layer were set to 1.8 parts by weight (the content of the titanium oxide: 10 wt %) and 16.2 parts by weight respectively to perform the image evaluation in the same manner as Example 31. Example 59 in Table 10 shows the results.
Furthermore, Examples 60 and 61 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 31 except that the mixing rate of the needle-like titanium oxide and binder resin in the undercoating layer was varied to set the content of the titanium oxide to 30 and 50 wt % respectively to perform the image evaluation in the same manner as Example 31. Examples 60 and 61 in Table 10 shows the results.
EXAMPLES 62 TO 64
Examples 62 to 64 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 31 except that binder resin in the coating solution for the undercoating layer was replaced with N-methoxymethyl nylon resin (manufactured by Teikoku chemical Industry Co., Ltd.: EF-30T) and that in the same manner as Examples 59 to 61 the mixing rate of the needle-like titanium oxide in the undercoating layer was varied to perform the image evaluation in the same manner as Example 31. Table 10 shows the results.
Comparative Examples 39 to 41
Comparative Examples 39 to 41 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 31 except that surface-untreated grain-like titanium oxide having a powder resistance of 10.sup.7 .OMEGA..multidot.cm and an average particle diameter of 0.03 .mu.m (manufactured by Ishihara Sangyo Kaisha, Ltd.: TTO-55N) and that the mixing rate of the grain-like titanium oxide in the undercoating layer was varied in the same manner as Examples 59 to 61 to perform the image evaluation in the same manner as Example 31. Table 10 shows the results.
Comparative Examples 42 to 44
Examples 42 to 44 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 31 except that grain-like titanium oxide was used in the same manner as Comparative Examples 39 to 41, that N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) was used as binder resin and that the mixing rate of the grain-like titanium oxide in the undercoating layer was varied in the same manner as Examples 59 to 61 to perform the image evaluation in the same manner as Example 31. Table 10 shows the, results.
EXAMPLES 65 TO 67
Examples 65 to 67 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 32 except that the mixing rate of the needle-like titanium oxide and the binder resin in the undercoating layer was varied to 10, 30 and 50 wt % respectively to perform the image evaluation in the same manner as Example 31. Table 11 shows the results.
EXAMPLES 68 TO 70
Examples 68 to 70 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 32 except that N-methoxymethyl nylon resin (manufactured by Teikoku Chemical Industry Co., Ltd.: EF-30T) was used as binder resin and that in the same manner as Examples 65 to 67 the mixing rate of the needle-like titanium oxide and the binder resin in the undercoating layer was varied to perform the image evaluation in the same manner as Example 31. Table 11 shows the results.
EXAMPLES 71 TO 73
Examples 71 to 73 of the function-separated electrophotographic photoconductor were formed in the same manner as Example 31 except that the needle-like titanium oxide and binder resin used in the coating solution for the undercoating layer were set to 9 parts by weight respectively and that the solvent contained in the coating solution for the undercoating layer was made of an azetropic composition comprising 10.33 parts by weight of methyl alcohol and 71.67 parts by weight of chloroform, one comprising 25.50 parts by weight of methyl alcohol and 56.50 parts by weight of tetrahydrofuran and one comprising 58.30 parts by weight of methyl alcohol and 23.70 parts by weight of toluene respectively to perform the image evaluation in the same manner as Example 31. Table 11 shows the results.
Specific products of needle-like titanium oxide used in the present invention include, other than the above products, surface-untreated rutile type titanium oxide such as FTL-100 (L=3 to 6 .mu.m, S=0.05 to 0.1 .mu.m, aspect ratio 30 to 120) and FTL-200 (L=4 to 12 .mu.m, S=0.05 to 0.15 .mu.m, aspect ratio 27 to 240) (manufactured by Ishihara Sangyo Kaisha, Ltd.), STR-60N (L=0.05 .mu.m, S=0.01 .mu.m, aspect ratio 5) (manufactured by Sakai Chemical Industry Co., Ltd.), rutile type titanium oxide coated with Al.sub.2 O.sub.3 such as STR-60 (L=0.05 .mu.m, S=0.01 .mu.m, aspect ratio 5), STR-60A (L=0.05 .mu.m, S=0.01 .mu.m, aspect ratio 5) surface-treated with Al.sub.2 O.sub.3 and SiO.sub.2 and STR-60S (L=0.05 .mu.m, S=0.01 .mu.m, aspect ratio 5) surface-treated with SiO.sub.2 (manufactured by Sakai Chemical Industry Co., Ltd.)
Besides, specific products of binder resin include, other than the above products, CM4000 (manufactured by Toray Industries, Inc.), F-30 and MF-30 (manufactured by Teikoku Chemical Industry Co., Ltd.) The present invention allows providing an electrophotographic photoconductor which has high sensitivity and a prolonged life with favorable image properties free from coating irregularities, by providing the undercoating layer using a coating solution which is a mixed solvent, preferably a mixed solvent of an azetropic composition of lower alcohol selected from a group comprising methyl alcohol, ethyl alcohol, isopropyl alcohol and n-propyl alcohol, and an organic solvent selected-from a group comprising dichloromethane, chloroform, 1,2-dichloroethane, 1,2-dichloropropane, toluene and tetrahydrofuran, when the undercoating layer cotains surface-untreated needle-like titanium oxide fine particles.
TABLE 1__________________________________________________________________________TiO.sub.2 binder initial value (-V) after 20000 cycle (-V)Example type W % resin environment V.sub.O V.sub.R V.sub.L V.sub.O V.sub.R V.sub.L__________________________________________________________________________1 A 10 a L/L 702 21 148 705 32 156 N/N 710 14 143 714 20 148 H/H 710 13 142 715 18 1472 A 50 a L/L 705 16 144 712 27 154 N/N 709 12 143 713 16 146 H/H 711 11 142 710 14 1453 A 80 a L/L 705 12 143 707 17 147 N/N 707 10 142 708 11 144 H/H 706 10 142 707 11 1434 A 95 a L/L 704 9 139 702 8 138 N/N 704 8 139 705 9 139 H/H 703 7 138 702 7 1385 A 99 a L/L 700 9 138 696 7 134 N/N 702 9 138 700 8 135 H/H 703 8 137 704 9 1386 A 10 b L/L 703 20 148 705 33 156 N/N 709 14 142 713 19 147 H/H 710 12 142 716 19 1487 A 50 b L/L 709 12 142 715 25 156 N/N 712 11 143 713 15 146 H/H 709 10 141 710 14 1448 A 80 b L/L 704 10 140 712 16 147 N/N 706 8 139 707 10 141 H/H 705 8 138 707 11 1409 A 95 b L/L 702 8 138 700 7 138 N/N 703 7 138 704 7 139 H/H 701 7 136 703 8 13810 A 99 b L/L 699 7 136 694 5 132 N/N 701 7 137 698 6 136 H/H 702 6 137 699 6 137__________________________________________________________________________ TiO.sub.2 A -- manufactured by Sakai Chemical Industry Co., Ltd.: STR60N, needlelike, not applied with surface tretment, 0.05 .times. 0.01 .mu.m binder resin a -- copolymer resin, manufactured by Toray Industries, Inc.: CM8000 b -- Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industry Co., Ltd.: EF30T
TABLE 2__________________________________________________________________________TiO.sub.2 binder initial value (-V) after 20000 cycle (-V)Example. type W % resin environment V.sub.O V.sub.R V.sub.L V.sub.O V.sub.R V.sub.L__________________________________________________________________________11 B 10 a L/L 705 24 150 713 35 159 N/N 712 16 144 716 22 149 H/H 711 13 142 714 20 14812 B 50 a L/L 706 19 146 714 29 153 N/N 709 14 145 716 19 147 H/H 710 12 142 713 15 14513 B 80 a L/L 704 11 143 709 18 147 N/N 706 10 142 707 12 144 H/H 704 10 141 706 11 14214 B 95 a L/L 702 9 140 700 8 139 N/N 701 8 139 703 8 139 H/H 700 8 139 701 9 14015 B 99 a L/L 698 8 135 696 7 134 N/N 701 8 138 703 8 136 H/H 700 7 137 701 8 13716 B 10 b L/L 707 25 150 711 33 157 N/N 706 15 144 714 20 151 H/H 707 13 142 712 19 14917 B 50 b L/L 706 18 147 715 29 154 N/N 712 14 143 716 20 146 H/H 706 11 142 712 14 14518 B 80 b L/L 704 13 144 710 19 148 N/N 707 11 143 711 13 145 H/H 704 9 140 706 12 14219 B 95 b L/L 701 10 141 701 9 140 N/N 703 8 139 704 8 141 H/H 705 8 140 706 8 14120 B 99 b L/L 699 9 136 697 7 134 N/N 701 8 136 703 8 136 H/H 703 7 135 704 7 136__________________________________________________________________________ TiO.sub.2 B -- manufactured by Ishihara Sangyo Kaisha, Ltd.: FTL100, needlelike, not applied with surface treatment, 3 to 6 .times. 0.05 to 0.1 .mu.m binder resin a -- copolymer resin, manufactured by Toray Industries, Inc.: CM8000 b -- Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industrys Co. Ltd.: EF30T
TABLE 3__________________________________________________________________________TiO.sub.2 binder initial value (-V) after 20000 cycle (-V)Example type W % resin environment V.sub.O V.sub.R V.sub.L V.sub.O V.sub.R V.sub.L__________________________________________________________________________21 C 10 a L/L 701 20 147 703 30 154 N/N 710 13 142 713 20 149 H/H 709 13 142 715 17 14622 C 50 a L/L 706 15 144 714 24 150 N/N 712 10 141 715 14 145 H/H 710 10 142 714 13 14423 C 80 a L/L 705 13 143 708 17 146 N/N 707 9 142 709 12 145 H/H 708 9 141 710 12 14424 C 95 a L/L 704 10 139 701 9 139 N/N 705 8 140 703 9 140 H/H 703 8 139 702 8 13825 C 99 a L/L 701 10 138 698 8 136 N/N 705 8 140 700 7 139 H/H 704 7 139 705 7 14026 C 10 b L/L 703 19 146 709 27 152 N/N 712 12 144 716 19 148 H/H 710 11 143 714 14 14527 C 50 b L/L 706 11 143 714 19 148 N/N 709 10 142 712 13 143 H/H 709 10 141 711 12 14228 C 80 b L/L 704 11 137 707 15 143 N/N 707 10 143 710 13 146 H/H 706 9 140 707 11 14129 C 95 b L/L 703 10 139 701 9 139 N/N 706 9 140 702 9 139 H/H 704 7 138 705 8 13830 C 99 b L/L 700 10 138 697 7 136 N/N 705 8 139 701 6 137 H/H 704 7 139 704 7 140__________________________________________________________________________ TiO.sub.2 C -- manufactured by Sakai Chemical Industry Co., Ltd.: STR60, needlelike, coated with Al.sub.2 O.sub.3, 0.05 .times. 0.01 .mu.m binder resin a -- copolymer resin, manufactured by Toray Industries, Inc.: CM8000 b -- Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industry Co., Ltd.: EF30
TABLE 4__________________________________________________________________________Comp. TiO.sub.2 binder initial value (-V) after 20000 cycle (-V)Ex. type W % resin environment V.sub.O V.sub.R V.sub.L V.sub.O V.sub.R V.sub.L__________________________________________________________________________1 D 10 a L/L 715 98 216 833 362 479 N/N 712 19 152 751 63 197 H/H 709 17 150 714 25 1572 D 50 a L/L 707 67 214 815 241 391 N/N 709 19 156 737 50 187 H/H 711 19 146 713 23 1483 D 80 a L/L 705 19 153 798 126 256 N/N 708 12 144 712 18 150 H/H 712 11 141 715 13 1424 D 95 a L/L 705 16 148 769 84 220 N/N 707 10 143 713 15 149 H/H 706 10 142 708 13 1445 D 99 a L/L 703 16 147 749 60 199 N/N 706 10 142 708 11 143 H/H 705 8 140 706 10 1416 D 10 b L/L 718 89 212 811 302 434 N/N 714 19 153 754 60 191 H/H 715 18 151 717 21 1527 D 50 b L/L 710 66 209 809 226 371 N/N 709 18 157 733 41 179 H/H 712 17 145 716 24 1528 D 80 b L/L 703 19 154 789 122 251 N/N 709 12 143 711 16 145 H/H 711 10 142 713 12 1439 D 95 b L/L 709 21 157 771 83 216 N/N 706 12 144 708 15 145 H/H 705 12 143 706 14 14210 D 99 b L/L 706 15 148 754 61 195 N/N 703 8 140 704 11 142 H/H 702 9 140 703 10 140__________________________________________________________________________ TiO.sub. 2 D -- manufactured by Ishihara Sangyo Kaisha, Ltd.: TTO55N, grainlike, not applied surface treatment, 0.03 .mu.m binder resin a -- copolymer resin, manufactured by Toray Industries, Inc.: CM8000 b -- Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industry Co., Ltd.: EF30T
TABLE 5__________________________________________________________________________Comp. TiO.sub.2 binder initial value (-V) after 20000 cycle (-V)Ex. W % resin environment V.sub.O V.sub.R V.sub.L V.sub.O V.sub.R V.sub.L__________________________________________________________________________11 E 10 a L/L 712 104 224 821 354 482 N/N 714 21 153 740 59 198 H/H 713 19 154 715 23 15712 E 50 a L/L 709 70 213 804 224 369 N/N 708 19 155 741 51 187 H/H 712 18 147 718 24 15213 E 80 a L/L 708 19 156 783 129 261 N/N 707 12 143 713 17 149 H/H 710 10 141 715 12 14314 E 95 a L/L 706 18 154 775 86 221 N/N 708 11 143 707 16 150 H/H 706 10 142 708 13 14415 E 99 a L/L 702 15 147 750 61 203 N/N 705 9 142 704 12 144 H/H 704 8 140 702 10 14216 E 10 b L/L 716 84 226 789 261 408 N/N 715 17 146 742 49 218 H/H 715 15 144 718 23 15017 E 50 b L/L 712 65 208 794 184 342 N/N 711 17 144 731 39 172 H/H 713 16 145 716 22 14918 E 80 b L/L 706 18 154 768 106 243 N/N 708 11 141 716 19 150 H/H 707 11 142 708 12 14319 E 95 b L/L 707 20 155 765 82 218 N/N 704 13 144 708 17 150 H/H 705 11 141 706 14 14220 E 99 b L/L 705 14 150 749 59 197 N/N 706 8 141 701 12 144 H/H 706 8 140 703 9 141__________________________________________________________________________ TiO.sub.2 E -- manufactured by Ishihara Sangyo Kaisha, Ltd.: TTO55A, grainlike, coated with Al.sub.2 O.sub.3, 0.03 .mu.m binder resin a -- copolymer resin, manufactured by Toray Industries, Inc.: CM8000 b -- Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industry Co., Ltd.: EF30T
TABLE 6__________________________________________________________________________Comp. TiO.sub.2 binder initial value (-V) after 20000 cycle (-V)Ex. type W % resin environment V.sub.O V.sub.R V.sub.L V.sub.O V.sub.R V.sub.L__________________________________________________________________________21 F 10 a L/L 659 18 109 125 2 18 N/N 662 10 101 139 2 15 H/H 658 9 102 146 2 1222 F 50 a L/L 621 15 92 101 2 13 N/N 631 9 85 97 1 14 H/H 635 8 86 99 1 1223 F 80 a L/L 601 7 82 83 1 10 N/N 624 6 80 79 1 12 H/H 621 6 81 81 1 1124 F 95 a L/L 593 5 79 80 1 11 N/N 598 4 78 81 0 10 H/H 595 4 79 83 1 1225 F 99 a L/L 536 4 75 75 1 10 N/N 524 3 72 72 0 9 H/H 528 4 74 76 0 926 F 10 b L/L 662 19 108 126 2 13 N/N 667 11 103 124 2 12 H/H 665 9 102 131 2 1027 F 50 b L/L 617 16 94 100 2 9 N/N 624 10 87 89 1 10 H/H 621 10 86 93 1 1128 F 80 b L/L 597 9 81 82 1 10 N/N 615 7 82 81 1 10 H/H 620 6 80 79 1 1129 F 95 b L/L 591 7 78 82 1 10 N/N 601 6 77 79 0 10 H/H 598 6 76 80 0 930 F 99 b L/L 536 5 72 75 0 9 N/N 526 5 71 71 0 9 H/H 525 4 73 74 0 9__________________________________________________________________________ TiO.sub. 2 F -- manufactured by Ishihara Sangyo Kaisha, Ltd.: FTL1000, needlelike, o which surface is rendered to be conductive by being treated with SnO.sub. (Sb doped), 3 to 6 .times. 0.05 to 0.1 .mu.m binder resin a -- copolymer resin, manufactured by Toray Industries, Inc.: CM8000 b -- Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industrys Co. Ltd.: EF30T
TABLE 7__________________________________________________________________________ solvent of coating solution for irregularities ofneedle-like undercoating layer coating solution for undercoating layer image irregularitiesPhotocon- TiO.sub.2 composition composition undercoating layer liquid irreg- liquid irreg- textureductor wt % part by weight part by weight dispersion pot life lopping ulation lopping ulation finess__________________________________________________________________________Example 31 95 methyl alcohol 28.70 1,2-dichloro- .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. ethane 53.30Example 32 95 methyl alcohol 43.46 1,2-dichloro- .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. propane 38.54Example 33 95 methyl alcohol 10.33 chloroform .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 71.67Example 34 95 methyl alcohol 25.50 tetrahydro- .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. furan 56.50Example 35 95 methyl alcohol 58.30 toluene 23.70 .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 36 95 methyl alcohol 41 1,2-dichloro- .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. ethane 41Example 37 95 methyl alcohol 41 1,2-dichloro- .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. propane 41Example 38 95 methyl alcohol 41 chloroform 41 .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 39 95 methyl alcohol 41 tetrahydro- .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. furan 41Example 40 95 methyl alcohol 41 toluene 41 .largecircle. 0 day .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Com. 95 methyl alcohol 82 -- X 0 day XX X X X XXEx. 31__________________________________________________________________________ Evaluation of dispersion: .largecircle. favorable .DELTA. practically acceptable X with aggregation Evaluation of irregularities: .largecircle. with no irregularities .DELTA. practically acceptable X with irregularities XX extremely inferior
TABLE 8__________________________________________________________________________ coating solution for irregularities of undercoating layer undercoating layer image irregularitiesPhotocon- storage pot liquid irreg- liquid irreg- textureductor stability life lopping ulation lopping ulation finess__________________________________________________________________________Example 41 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 42 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 43 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 44 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 45 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 46 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 47 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 48 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 49 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .DELTA.Example 50 .largecircle. 30 days .largecircle. .largecircle. .largecircle. .largecircle. .DELTA.Com. Ex. 32 X 30 days XX X X X XX__________________________________________________________________________ Evaluation of storage stability: .largecircle. favorable .DELTA. practically acceptable X with aggregation Evaluation of irregularities: .largecircle. with no irregularities .DELTA. practically acceptable X with irregularities XX extremely inferior
TABLE 9______________________________________Photocon-ductor pot life turbidity______________________________________Example 51 0 day 53Example 52 30 days 58Example 53 0 day 60Example 54 30 days 67Com. Ex. 33 0 day 395Com. Ex. 34 30 days partially aggregated and sedimentatedCom. Ex. 35 0 day totally aggregated and sedimentated______________________________________
TABLE 10__________________________________________________________________________ irregularities of undercoating layer image irregularitiesPhotocon- TiO.sub.2 binder liquid irreg- liquid irreg- texture overlappingductor type wt % resin lopping ulation lopping ulation finess in white portion__________________________________________________________________________Example 59 A 10 a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 60 A 30 a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 61 A 50 a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 62 A 10 b .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 63 A 30 b .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Example 64 A 50 b .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle.Com. Ex. 39 B 10 a .DELTA. X .DELTA. X XX XXCom. Ex. 40 B 30 a X X X X X XXCom. Ex. 41 B 50 a X X X X X XCom. Ex. 42 B 10 b .DELTA. X .DELTA. X X XXCom. Ex. 43 B 30 b X X X X XX XXCom. Ex. 44 B 50 b X X X X X X__________________________________________________________________________ TiO.sub.2 A: manufactured by Sakai Chemical Industry Co., Ltd.: STR60N needlelike, not applied with surface treatment B: manufactured by Ishihara Sangyo Kaisha, Ltd.: TTO55N grainlike, not applied with surface treatment binder resin a: copolymer nylon, manufactured by Toray Industries, Inc.: CM 8000 b: Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industry Co., Ltd.: EF30T Evaluation of irregularities: .largecircle. with no irregularities .DELTA. practically acceptable X with irregularities XX extremely inferior
TABLE 11__________________________________________________________________________ solvent of coating solution for irregularities of undercoating layer undercoating layer image irregularitiesPhotocon- TiO.sub.2 composition composition binder liquid irreg- liquid irreg- texture overlappingductor type wt % part by weight part by weight resin lopping ulation lopping ulation finess in white__________________________________________________________________________ portionExample 65 A 10 methyl alcohol 1,2-dichloro- a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 43.46 propane 38.54Example 66 A 30 methyl alcohol 1,2-dichloro- a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 43.46 propane 38.54Example 67 A 50 methyl alcohol 1,2-dichloro- a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 43.46 propane 38.54Example 68 A 10 methyl alcohol 1,2-dichloro- b .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 43.46 propane 38.54Example 69 A 30 methyl alcohol 1,2-dichloro- b .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 43.46 propane 38.54Example 70 A 50 methyl alcohol 1,2-dichloro- b .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 43.46 propane 38.54Example 71 A 50 methyl alcohol chloroform a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 10.33 71.67Example 72 A 50 methyl alcohol tetrahydrofuran a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 25.50 56.50Example 73 A 50 methyl alcohol toluene 23.70 a .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. .largecircle. 58.30__________________________________________________________________________ TiO.sub.2 A: manufactured by Sakai Chemical Industry Co., Ltd.: STR60N needlelike, not applied with surface treatment binder resin a: copolymer nylon, manufactured by Toray Industries, Inc.: CM 8000 b: Nmethoxymethyl nylon, manufactured by Teikoku Chemical Industry Co., Ltd.: EF30T Evaluation of irregularities: .largecircle. with no irregularities .DELTA. practically acceptable X with irregularities XX extremely inferior

Number	Date	Country	Kind
5-178916	Jul 1993	JPX
6-161611	Jul 1994	JPX

Number	Name	Date
4377629	Tarumi et al.	Mar 1983
4518669	Yashiki	May 1985
4775605	Seki et al.	Oct 1988

Number	Date	Country
0576957	Jan 1994	EPX
51-114132	Oct 1976	JPX
55-25030	Feb 1980	JPX
56-52757	Dec 1981	JPX
58-95351	Jun 1983	JPX
59-93453	May 1984	JPX
63-234261	Sep 1988	JPX
298251	Dec 1988	JPX
63-298251	Dec 1988	JPX
2-181158	Jul 1990	JPX
181158	Jul 1990	JPX

Electrophotographic photoconductor and a method for forming the same

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (2)

US Referenced Citations (3)

Foreign Referenced Citations (11)