Electrophotographic photoconductor and method for...

Radiation imagery chemistry: process – composition – or product th – Electric or magnetic imagery – e.g. – xerography,... – Radiation-sensitive composition or product

Reexamination Certificate

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C430S078000, C430S134000

Reexamination Certificate

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06489072

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to an electrophotographic photoconductor (also referred to as “a photoconductor”) used in a printer, a copier, or a facsimile machine that employs an electrophotographic process. In particular, the invention relates to a photoconductor that comprises an improved photosensitive material in a photosensitive layer, thereby exhibiting an excellent potential retention rate. The invention also relates to a method for manufacturing such a photoconductor.
2. Description of the Related Art
It is generally known that electrophotographic photoconductors provide the function of maintaining surface charges in the dark, generating charges upon receipt of light, and transporting charges upon receipt of light. Known types of photoconductors include single-layer type photoconductors having all of these functions in a single layer. Also know are laminated-layer type photoconductors consisting of function-separated two layers, where one layer mainly serves to generate charges and another layer serves to maintain surface charges in the dark and to transport charges upon receipt of light.
These types of photoconductors are used for forming images by known electrophotographic methods, such as the Carlson method. Image formation using this method includes the steps of charging the photoconductor by a corona discharge in the dark, forming an electrostatic latent image, such as characters or drawings of an original, on the charged surface of the photoconductor, developing the thus formed electrostatic image by means of toner powder, transferring and fixing the toner powder representing the image onto a support, such as paper.
After the toner transfer, the residual toner powder is removed, and residual charges are erased by light exposure, so that the photoconductor can be used again.
Various substances have been employed as photosensitive materials in electrophotographic photoconductors. For example, inorganic photoconductive substances include selenium, selenium alloys, zinc oxide and cadmium sulfide, dispersed in a resin binder, as well as organic photoconductive substances, such as poly-N-vinylcarbazole, poly(vinyl anthracene), phthalocyanine compound or bisazo compound, dispersed in a resin binder or subjected to vacuum deposition.
Among the organic photosensitive substances described above, the phthalocyanine compound exhibits quite different electrophotographic properties depending its crystal form. A variety of studies have investigated this substance.
Methods for applying the phthalocyanine compounds have been reported not only in cases where one type of that compound is used, but also in cases where two or more types of that compound are used as a mixture.
Uses of two or more types of phthalocyanine compounds by intentional mixing are disclosed in Japanese Unexamined Patent Application Publication (KOKAI) Nos. H2-170166, H2-84661, and H6-145550. Unfortunately, the mixed use of the phthalocyanines in these references was only aiming at a simple use of mixed crystals. No reference discloses a study on difference in positive or negative charge generating ability in a charge generation process of the mixed materials. Xabq
The mixed use of two or more phthalocyanine compounds can be unintentionally conducted by generation of side products during the synthesis process of phthalocyanine. Japanese Unexamined Patent Application Publication (KOKAI) No. H3-35245, discloses discussions on side production of titanyloxo(chlorophthalocyanine) in the synthesis process of titanyloxophthalocyanine. This reference discloses that inclusion of 0.38 to 5 wt % of chlorine is confirmed in the patent documents published in the past. The reference further discloses a detailed study on a synthesis method of titanyloxophthalocyanine that does not generate a side product of chlorine-containing phthalocyanine.
According to the references, titanyloxophthalocyanine with high purity and without lattice defects may be obtained by suppressing generation of the side product of chlorine-containing phthalocyanine. As a result, photoconductors with excellent potential retention capability and high sensitivity may be generated. Unfortunately, the references do not disclose changes in charge generation mechanisms in a case where two types of phthalocyanines are included. The references also do not mention change of potential retention rate depending on the ratio of the contents of the two phthalocyanines in consideration of a charge generation mechanism.
Metal-free phthalocyanines are also studied in terms of various synthesis methods and purification methods, and are disclosed in Japanese Unexamined Patent Application Publication (KOKAI) Nos. H7-2071883 and S60-243089.
These references do not disclose or consider impurities from phthalocyanine derivatives. As a result, no study has been made about variation of charge generation mechanisms due to containment of impurities of phthalocyanine derivatives.
It is known that photoconductors include negative-charging laminated-layer-type photoconductors, positive-charging laminated-layer-type photoconductors, and positive-charging single-layer-type photoconductors.
Synthesis methods of phthalocyanine compound are disclosed in “Phthalocyanines” by C. C. Leznoff et al., 1989, VCH Publishers, Inc. and “The phthalocyanines” by F. H. Moser et al., 1983, CRC Press, for example. By-production of derivatives in the synthesis process of titanyloxophthalocyanine is disclosed in Japanese Unexamined Patent Application Publication No. H3-35245. A titanylphthalocyanine complex compound may be synthesized by the method disclosed in Japanese Unexamined Patent Application Publication No. H8-302223 or No. H9-230615.
The use of a phthalocyanine compound as a photosensitive material in a photoconductor is known. Methods of synthesis and use of these compound have been studied in some aspects. Unfortunately, a relationship between a charge generation mechanism and a potential retention rate has not been understood or clarified in mixed uses of two or more types of phthalocyanine compounds.
OBJECTS AND SUMMARY OF THE INVENTION
It is an object of the present invention to provide a photoconductor with excellent photoconductive characteristics.
It is another object of the present invention to provide, in particular, an excellent potential retention rates in a photoconductor.
It is another object of the invention to provide a method for manufacturing a photoconductor, the method comprising a step for forming a photosensitive layer with coating liquid and forming a photosensitive layer with an excellent potential retention rate.
Briefly stated, the present invention relates to an electrophotographic photoconductor and manufacturing method. The electrophotographic photoconductor includes a conductive substrate and a photosensitive layer formed on a substrate. The photosensitive layer includes at least a phthalocyanine compound as a charge generation substance. The photosensitive layer contains a first phthalocyanine compound as a main component and a second phthalocyanine compound as a secondary component and as a result, has greater ability to generate negative charges than the ability of the first phthalocyanine compound.
It is to be understood, that to solve the above-described problems, the inventors have made rigorous studies considering the negative-charge-generating ability of the phthalocyanine compound in the charge generation mechanism, and surprisingly found, as a result, that the potential retention rate of a photoconductor significantly increases when second phthalocyanine compound, having higher ability to generate negative charges than that of first phthalocyanine compound, is contained as a secondary component in the photosensitive layer including the first phthalocyanine compound as a charge generation substance.
It is to be further understood, that a potential retention rate of a photoconductor significantly increases when a phthalocyanine compound as a secondary component of charge generation substance is contained

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