US3095301A - Electrophotographic element - Google Patents
Electrophotographic element Download PDFInfo
- Publication number
- US3095301A US3095301A US804411A US80441159A US3095301A US 3095301 A US3095301 A US 3095301A US 804411 A US804411 A US 804411A US 80441159 A US80441159 A US 80441159A US 3095301 A US3095301 A US 3095301A
- Authority
- US
- United States
- Prior art keywords
- amino
- methyl
- butanol
- layer
- electrophotographic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 17
- 239000011230 binding agent Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 16
- 239000011248 coating agent Substances 0.000 claims description 14
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 13
- -1 3-AMINO-1 Chemical compound 0.000 claims description 11
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 claims description 10
- 239000011787 zinc oxide Substances 0.000 claims description 8
- LXQMHOKEXZETKB-UHFFFAOYSA-N 1-amino-2-methylpropan-2-ol Chemical compound CC(C)(O)CN LXQMHOKEXZETKB-UHFFFAOYSA-N 0.000 claims description 4
- KYUPIHBUKDNZKE-UHFFFAOYSA-N 1-amino-3-methylbutan-2-ol Chemical compound CC(C)C(O)CN KYUPIHBUKDNZKE-UHFFFAOYSA-N 0.000 claims description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 3
- QHKGDMNPQAZMKD-UHFFFAOYSA-N 2-amino-2-methylbutan-1-ol Chemical compound CCC(C)(N)CO QHKGDMNPQAZMKD-UHFFFAOYSA-N 0.000 claims description 3
- NFZHDQFMWNCLMM-UHFFFAOYSA-N 2-amino-2-methylpentan-3-ol Chemical compound CCC(O)C(C)(C)N NFZHDQFMWNCLMM-UHFFFAOYSA-N 0.000 claims description 3
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 claims description 3
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 claims description 3
- ULAXUFGARZZKTK-UHFFFAOYSA-N 2-aminopentan-1-ol Chemical compound CCCC(N)CO ULAXUFGARZZKTK-UHFFFAOYSA-N 0.000 claims description 3
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 claims description 3
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims description 3
- IOAOAKDONABGPZ-UHFFFAOYSA-N 2-amino-2-ethylpropane-1,3-diol Chemical compound CCC(N)(CO)CO IOAOAKDONABGPZ-UHFFFAOYSA-N 0.000 claims description 2
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 claims description 2
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 claims description 2
- OZSQDNCDEHVGBC-UHFFFAOYSA-N 3-amino-2,3-dimethylbutan-2-ol Chemical compound CC(C)(N)C(C)(C)O OZSQDNCDEHVGBC-UHFFFAOYSA-N 0.000 claims description 2
- LHYVEOGDJNQNEW-UHFFFAOYSA-N 1-amino-2-methylbutan-2-ol Chemical compound CCC(C)(O)CN LHYVEOGDJNQNEW-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 description 31
- 238000000034 method Methods 0.000 description 19
- 239000000123 paper Substances 0.000 description 12
- 230000008569 process Effects 0.000 description 10
- 239000000975 dye Substances 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000005855 radiation Effects 0.000 description 6
- 150000001414 amino alcohols Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920002050 silicone resin Polymers 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- BTANRVKWQNVYAZ-UHFFFAOYSA-N 2-butanol Substances CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052711 selenium Inorganic materials 0.000 description 3
- 239000011669 selenium Substances 0.000 description 3
- 230000001235 sensitizing effect Effects 0.000 description 3
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000005083 Zinc sulfide Substances 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 229930187593 rose bengal Natural products 0.000 description 2
- 229940081623 rose bengal Drugs 0.000 description 2
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052984 zinc sulfide Inorganic materials 0.000 description 2
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N 1-propanol Substances CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methyl-2-butanol Substances CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- MXLMTQWGSQIYOW-UHFFFAOYSA-N 3-methyl-2-butanol Substances CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DPKHZNPWBDQZCN-UHFFFAOYSA-N acridine orange free base Chemical compound C1=CC(N(C)C)=CC2=NC3=CC(N(C)C)=CC=C3C=C21 DPKHZNPWBDQZCN-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- DZBUGLKDJFMEHC-UHFFFAOYSA-N benzoquinolinylidene Natural products C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- CEJANLKHJMMNQB-UHFFFAOYSA-M cryptocyanin Chemical compound [I-].C12=CC=CC=C2N(CC)C=CC1=CC=CC1=CC=[N+](CC)C2=CC=CC=C12 CEJANLKHJMMNQB-UHFFFAOYSA-M 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- VYQMZUUUGRXQHR-UHFFFAOYSA-N magnesium;oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[Mg+2].[Ti+4] VYQMZUUUGRXQHR-UHFFFAOYSA-N 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- DWCZIOOZPIDHAB-UHFFFAOYSA-L methyl green Chemical compound [Cl-].[Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)[N+](C)(C)C)=C1C=CC(=[N+](C)C)C=C1 DWCZIOOZPIDHAB-UHFFFAOYSA-L 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 125000004971 nitroalkyl group Chemical group 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000002601 radiography Methods 0.000 description 1
- 230000003716 rejuvenation Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical compound [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- UQMZPFKLYHOJDL-UHFFFAOYSA-N zinc;cadmium(2+);disulfide Chemical compound [S-2].[S-2].[Zn+2].[Cd+2] UQMZPFKLYHOJDL-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/10—Bases for charge-receiving or other layers
- G03G5/101—Paper bases
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/142—Inert intermediate layers
Definitions
- This invention relates to the general art of electrophotography and electroradiography and particularly to a new and improved electrostatic recording element and a method of producing same. More specifically, the invention relates to an electrophotographic member having a backing or support rendered electrically conductive by means of certain surface active compounds.
- a base plate or support is coated with a layer of photoconducting material which is then electrostatically charged in the dark.
- the charged layer is next exposed to light beneath a pattern such as a negative photographic film, positive film or a mask or other suitable light image whereupon a latent electrostatic image is formed upon the photoconduetive surface.
- a latent image is produced by the dissipation of the electric charges in proportion to the intensity of light to which any given area of the photoconductive layer is exposed.
- Development consists in dust-ing an electrically charged powder on the coating in the dark which adheres to the areas of high electrostatic charge (corresponding to low exposure) while the powder clings only slightly or not at all in the neutralized or discharged areas (corresponding to high exposure).
- the image can then be transferred to a suitable receiving material in order to obtain a positive or negative print as the case may be. 7
- the recording element is commonly constructed in two different ways.
- a layer or film of the photoconductive material is applied directly to a conductive metal backing member as exemplified by the type of construction known in the art as a xerographic plate.
- the photoconductor may be em- .ployed in the form of minute particles dispersed in an electrically insulating binder and applied to asuitable backing member.
- xerographic plates is attendant with several disadvantages, chief among which is the need for making a transfer copy since the original electrophotogr-aphic recording element would be too bulky and expensive and generally unsuitable as a material for perlayer is very thin and also .very soft, it isv easily abraded or scratched during ordinary service and such defects are transferred to the final prints produced therefrom. Furthermore, such plates exhibit -a fatigue eltect after continued usage. This property or characteristic can be attributed to incomplete neutralization of the electrostatic charge on exposure to light resulting in a certain amount of permanent residual background charge. As a consequence, the residual charge attracts some of the developing powder giving rise to images and prints displaying darkened or foggy backgrounds. Although the plates may be rejuvenated by subjecting them to an electrostatic charge opposite in sign to the original charge so as to neutralize the residual background charge, this requires extra time and steps which are undesirable in commercial installations.
- electrophotographic plates wherein the photoconductor is dispersed in an electrically insulating binder can be produced which do not possess the disadvantages associated with the aforementioned xerographic plates.
- the light-sensitive layer containing the dispersed photoconductor may be coated directly on a convenient base material such as paper, exposed to light through a pattern and the resulting electrostatic image developed to yield a print immediately usable without resorting to a transfer process at any time.
- Such electrostatic recording elements are easy to manufacture and do not require expensive and elaborate processing equipment.
- Another object of the invention is to provide a method for coating the base of an electrophotographic recording element with a composition which will increase the electrical conductivity of said base plate.
- a further object of the invention is to provide a methed for the production of electrostatic images directly on a suitable recording material without having to subsequently transfer the first image to a receiving material.
- R R R and R represent hydrogen, lower alkyl and lower alkylol groups.
- Aminoalcohols are known compounds and can be found in the chemical literature. Generally, their preparation involves reduction of the corresponding nitroalkane.
- aminoalcohols of the type suitable for practicing the invention include:
- the invention comprises precoating a nonmetallic support such as paper with the aforesaid aminoalcohol after which the coating is allowed to dry. Over the precoating layer is then applied a second coating of a photoconducting material of the type wherein the photoconductor is suspended in the form of minute particles in an electrically insulating binding material having an electrical resistivity of about to 10 ohms centimeter.
- the resulting electrophotographic plate can then be electrostatically charged and developed in the manner commonly employed in the art.
- the so obtained prints are free of background fog and the use of a paper base in lieu of the usual metallic backing member results in the prints being immediately usable without resorting to any transfer processes.
- An electrophotographic element of the latter type embodies a fluorescent intensifying layer or screen interposed between the support and the photoconducting layer.
- a fluorescent screen comprises a dispersion of fluorescent particles in a resin binder. Due to the rather high dielectric properties of the binder, the fluorescent screen also acts as an insulating layer between the support and photoconducting layer. As a consequence, when such a plate is exposed to an optical image, dissipation or conduction of the electric charges away from the exposed areas is hindered.
- such a double layer coating can be made to function efficiently by dispersing particles of the fluorescent material in a lower molecular weight aminoalochol described above. Since the fluorescent particles are dispersed in a conducting environment, electrophotographic recording elements embodying this feature allow for easy dissipation and removal of the electric charges with the subsequent production of electrophotographic prints and fog-free background.
- FIGS. 1 and 2 represent sectional views of an electrophotographic member constructed in accordance with our invention.
- a base plate 1. of paper has precoated thereon a layer 2 of an aminoalcohol described above which, in turn, is overlayed with a photoconductive insulating layer 3 comprising an electrical insulating binder 4 having dispersed therein particles of a photoconducting material 5.
- 1 is a base or backing support; 6 represents a fluorescent layer comprising an aminoalcohol matrix 2 having imbedded or dispersed therein particles of a fluorescent material 7; and 3 is a photoconductive layer in which the photoconducting material 5 is dispersed or distributed throughout an electrically insulating binder 4.
- photoconductors which we can employ for the purpose described herein include zinc oxide, sulfur, anthracene, anthraq-uinone, lead oxide, lead iodide, cadmium sulfide, cadmium selenide and the like.
- sensitizing dyes may be selected for the purpose of increasing the speed of the spectral response of a photoconductive material by extending or increasing the characteristic or inherent absorption of the photoconducting material itself.
- a dye may be selected for the purpose of sensitizing the photoconducting material to a different portion of the spectrum and thus extend the band of frequencies to which the photoconducting material will respond.
- the dyes which have been suggested as sensitizers for use in electrophotography are the phthalein type dyes such as rose bengal, the triphenylmethane dyes such as malachite green and methyl green, the cyanine dyes such as kryptocyanine, acridine orange as well as many others.
- a coating composition containing one of the aforesaid aminoalcohols is prepared by dissolving the appropriate aminoalcohol in a suitable solvent and the resulting mixture coated on a non-metallic base of the type previously described.
- various adjuncts may be desirable to add to the composition in order to facilitate the coating operation.
- Example 1 A paper base having a resistivity of 1.5 l ohms centimeter was coated with the following composition: An aminoalcohol of the type described above g Toluene ml and then allowed to dry.
- a second coating consisting of a dispersion of a photoconductor in a binder was prepared as follows: 20 g. of zinc oxide, 16 g. of silicone resin and 20 g. of toluene were placed in a porcelain ball-mill of one quart capacity half filled with 0.5 in. porcelainb'alls and milled for about two hours. The mixture was then coated by applicator roller method on the above subbed paper base and allowed to dry. The thickness of the photo-conductive layer was about 10 microns. An electrostatic charge was placed on the plate and exposed to radiation to effect discharge of the plate. The residual surface charge was then measured using a dynamic electrometer. A second electrophotographic plate was prepared as above except the paper base was not treated with the aminoalcohol. On charging and exposing, the residual surface charge on the second plate was much higher than in the case of the first plate.
- the silicone resin was obtained on the commercial market as GE Silicone Resin SR-82, a product of the General Electric Company, Pittsfield, Mass.
- the zinc oxide photoconductor was purchased commercially as French Process Florence Green Seal Pigment Grade, 2. product of the New Jersey Zinc Sales Company, Inc., New York, New York.
- Example 2 The same procedure was followed as given in Example 1 excepting that the zinc oxide photoconductor was sensitized to the green portion of the spectrum with rose bengal dye. 0.01 gram of sensitizer was added to the zinc oxide dispersion during the ball-milling stage.
- Example 3 15 grams of zinc sulfide (copper and cobalt activated) and 20 g. of the aminoalcohol solution of Example 1 was ball-milled for two hours. The resulting dispersion of fluorescent agent was then coated on a metal base using the applicator roller method. The thickness of the layer amounted to about 10 microns. A photoconductive layer of the type described in Example 2 was next applied over the first layer and allowed to dry. The resulting electrophotographic recording element containing an intermediate fluorescent layer interposed between the base and photoconductive layer is particularly valuable in the field of radiography wherein the exciting radiation are X-rays. In operation, the element is first electrostatically charged in the usual manner and then exposed to an X-ray pattern or image.
- the electrostatic charges comprising the latent image are neutralized.
- the X-rays cause the fluorescent layer to emit light which neutralizes more of the electrostatic charges.
- Example 4 The same procedure was employed as given in Example 3 excepting that the metal base was replaced by a paper base. I
- the fluorescent material is selected from the class consisting of copper activated zinc sulfide, copper and cobalt acti- Vated zinc sulfide, silver activated zinc sulfide, zinc cadmium sulfide, magnesium titanium dioxide, calcium tungstate and cesium halide.
- An electrophotographic member comprising a nonmetallic base plate of high electrical resistance, a coating on said base plate for increasing the electrical conductivity of the plate, said coating comprising an aminoalcohol selected from the group consisting of Z-amino-I-butanol, 2-amino-2-methyl-l-propanol, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-ethyl-1,3-propanediol, tris(hy-droxymethyl)aminomethane, 2-amino-2-methyl-1-butanol, 2- amino-l-ethanol, 3-amino-2,3-dimethyl-2-butanol, l-amino-2-methyl-2-butanol, 1-amino-3-methyl-2-butanol, 2- amino-l-propanol, l-amino-2-methyl-2-propanol, Z-aminol-pentanol, 3-amino-1,2-p
- An electrophotographic member comprising a nonmetallic base plate of high electrical resistivity, an intermediate fluorescent layer bonded to said plate and an upper layer comprising a zinc oxide photoconductor uniformly dispersed in an electrically insulating filmforming binder having an electrical resistance higher than that of the base plate and photoconductor, the fluorescent layer comprising a fluorescent material uniformly dispersed throughout an aminoalcohol selected from the group consisting of 2-amino-l-butanol, 2-amino-2-methyll-propanol, Z-amino-Z-methyl-1,3-propanediol, Z-amino- 2 ethyl-1,3-propanediol, tris(hydroxymethyl)aminomethane, 2-amino-2-methyl-l-butanol, Z-amino-l-ethanol, 3- amino-Z,3-dimethyl-2-butanol, l-amino-Z-methyl-Z-butan01, 1-amino-3-methyl-2-
- an electrophotographic process comprising placing an electrostatic charge on the surface of an electrophotographic member comprising a non-metallic base plate, a layer thereon comprising a zinc oxide photoconductor uniformly dispersed in an electrically insulating film-forming binder having an electrical resistance higher than that of the base plate and photoconductor; selectively neutralizing the electrostatic charge from the surface of the charged photoconductive insulating layer by exposing said charged layer to radiation of a wave length ranging from 10- centimeters to 1O centimeters thereby creating an electrostatic latent image on the surface of the photoconducting insulating layer and developing said electrostatic latent image with electrically charged powder particles, the improvement of applying to the base plate in order to increase its electrical conductivity, an aminoalcohol selected from the group consisting of Z-amino-I-butanol, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-ethyl- 1,
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- Physics & Mathematics (AREA)
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- Photoreceptors In Electrophotography (AREA)
Description
June 25, 1963 J. KOSTELEC ETAL ELECTROPHOTOGRAPHIC ELEMENT Filed April 6, 1959 FIGJ FIG.2
PHOTOCONDUCTIVE LAYER INSULATING BINDER PHOTOCONDUCTING MATERIAL LOW MOLECULAR WEIGHT AMINO ALCOHOL BASE INSULATING BINDER PI-Io ocoNDucTINe MATERIAL PHOTO CONDUCTIVE LAYER FLUORESCENT MATERIAL LOW MOLECULAR WEIGHT AMINO ALCOHOL FLUORESCENT LAYER ATTORNEYS United States Patent Ofice 3,095,301 Patented June 25, 1963 3,095,301 ELECTROPHOTOGRAPHIC ELEMENT Joie Kostelec and Heinz F. Nitka, Binghamton, N.Y., assignors to General Aniline 8: Film Corporation, New York, N.Y., a corporation of Delaware Filed Apr. 6, 1959, Ser. No. 804,411v 11 Claims. (Cl. 96-1) This invention relates to the general art of electrophotography and electroradiography and particularly to a new and improved electrostatic recording element and a method of producing same. More specifically, the invention relates to an electrophotographic member having a backing or support rendered electrically conductive by means of certain surface active compounds.
In the art of producing images or visible records by electrophotographic, methods, a base plate or support is coated with a layer of photoconducting material which is then electrostatically charged in the dark. The charged layer is next exposed to light beneath a pattern such as a negative photographic film, positive film or a mask or other suitable light image whereupon a latent electrostatic image is formed upon the photoconduetive surface. Such a latent image is produced by the dissipation of the electric charges in proportion to the intensity of light to which any given area of the photoconductive layer is exposed.
Development consists in dust-ing an electrically charged powder on the coating in the dark which adheres to the areas of high electrostatic charge (corresponding to low exposure) while the powder clings only slightly or not at all in the neutralized or discharged areas (corresponding to high exposure). The image can then be transferred to a suitable receiving material in order to obtain a positive or negative print as the case may be. 7
In addition to light, other types of actinic radiations are also capable of producing electrostatic latent images on a charged surface of a photoconductor and in this connection mention is made of ultraviolet light, X-rays, gamma rays and the like. When electrophotographic plates are used in conjunction with X-rays, the process is known as electroradiography.
In electrophotographic processes generally described above, the recording element is commonly constructed in two different ways. In one arrangement, a layer or film of the photoconductive material is applied directly to a conductive metal backing member as exemplified by the type of construction known in the art as a xerographic plate. Alternately, the photoconductor may be em- .ployed in the form of minute particles dispersed in an electrically insulating binder and applied to asuitable backing member.
Of the two methods, the latter offers advantages in economy and convenience over the xerographic plate as is evident from the following comparison. The manu facture of xerographic plates is at best a costly and highly technical process. The metal plates must be specially treated in order to assure a scrupulously clean surface after which the selenium photoconducting layer is applied by an evaporation technique. This operation must be carried out under the most vigorously controlled conditions particularly as regards to the rate of evaporation of the selenium and the even distribution and proper thickness of the selenium coating. The fact that the entire undertaking must be conducted under high vacuum greatly contributes to the cost of manufacture.
Furthermore, the use of xerographic plates is attendant with several disadvantages, chief among which is the need for making a transfer copy since the original electrophotogr-aphic recording element would be too bulky and expensive and generally unsuitable as a material for perlayer is very thin and also .very soft, it isv easily abraded or scratched during ordinary service and such defects are transferred to the final prints produced therefrom. Furthermore, such plates exhibit -a fatigue eltect after continued usage. This property or characteristic can be attributed to incomplete neutralization of the electrostatic charge on exposure to light resulting in a certain amount of permanent residual background charge. As a consequence, the residual charge attracts some of the developing powder giving rise to images and prints displaying darkened or foggy backgrounds. Although the plates may be rejuvenated by subjecting them to an electrostatic charge opposite in sign to the original charge so as to neutralize the residual background charge, this requires extra time and steps which are undesirable in commercial installations.
On the other hand, electrophotographic plates wherein the photoconductor is dispersed in an electrically insulating binder can be produced which do not possess the disadvantages associated with the aforementioned xerographic plates. The light-sensitive layer containing the dispersed photoconductor may be coated directly on a convenient base material such as paper, exposed to light through a pattern and the resulting electrostatic image developed to yield a print immediately usable without resorting to a transfer process at any time. Such electrostatic recording elements are easy to manufacture and do not require expensive and elaborate processing equipment.
Furthermore, since the original recording material bemetallic backing were limited in their scope and application because of rather high background fog. This situation is due to the poor electrical conductivity of a nonrnetallic support which retards conduction of the neutralized electrical charges away from the exposed areas of the plate. Consequently, a certain residual background.
charge remains which attracts the developing powder to produce. the foggy. images previously mentioned.
It is believed to be manifest that the art is in need of an eleotrophotographic. recording. member capable of yielding fog-free prints directly which is, at the same time, economical to manufacture and which is easy to use and operate.
It is, therefore, an object of this invention to provide an electrophotographic recording element wherein the photoconductive material is coated on a non-metallic conductive backing. V
Another object of the invention is to providea method for coating the base of an electrophotographic recording element with a composition which will increase the electrical conductivity of said base plate.
A further object of the invention is to provide a methed for the production of electrostatic images directly on a suitable recording material without having to subsequently transfer the first image to a receiving material.
Other objects and purposes of the invention will be apparent as the description proceeds.
It has now been found that an improved, eflicient and economical electrophotographic plate can. be produced by treating a non-metallic base plate material with an aminoalcohol of the following formula:
wherein R R R and R represent hydrogen, lower alkyl and lower alkylol groups.
3 Aminoalcohols are known compounds and can be found in the chemical literature. Generally, their preparation involves reduction of the corresponding nitroalkane.
Examples of aminoalcohols of the type suitable for practicing the invention include:
2-amino-1-butanol Z-amino-Z-methyl-l-propanol 2-amino-2-methyl-1,3-propanediol 2-amino-2-ethyl-1,3-propanediol tris(hydroxymethyl) aminomethane 2-amino-2-methyl-l-butanol Z-amino-l-ethanol 3-amino-2,3-dimethyl-2-butanol 1-amino-2-methyl-2-butanol 1-amino-3-rnethyl-2-butanol 2-amino-1-propanol 1-amino-2methyl-2-propanol Z-amino-l-pentanol 3-a-mino-1,2-pentanol Z-amino-Z-methyl-3-pentanol Typical backing materials which are suitable for practicing our invention include paper, cloth, wood, plastic, leather and the like. We prefer to use paper as a support for our electrophotographic images since it is economical, readily obtainable as well as convenient to handle, store and file.
In general, the invention comprises precoating a nonmetallic support such as paper with the aforesaid aminoalcohol after which the coating is allowed to dry. Over the precoating layer is then applied a second coating of a photoconducting material of the type wherein the photoconductor is suspended in the form of minute particles in an electrically insulating binding material having an electrical resistivity of about to 10 ohms centimeter. The resulting electrophotographic plate can then be electrostatically charged and developed in the manner commonly employed in the art. The so obtained prints are free of background fog and the use of a paper base in lieu of the usual metallic backing member results in the prints being immediately usable without resorting to any transfer processes.
The manner of preparing electrophotographic plates wherein the photoconductor is suspended or dispersed in an electrically insulating binder is described in the prior art and in this connection reference is made to U.S.P. 2,663,636. Briefly, such a process comprises mixing and grinding together, in a ball-mill or other suitable comminuting equipment, a photoconducting material together with a solvent and a binder material having an electrical volume resistivity of about 10 to 10 ohms centimeter for a period of time suflicient to effect reduction to the desired particle size.
Our invention is particularly valuable when incorporated in electrophotographic elements having a built-in intensifying screen of the type described in U.S. copending application Serial Number 751,968, filed July 30, 1958. An electrophotographic element of the latter type embodies a fluorescent intensifying layer or screen interposed between the support and the photoconducting layer. Such a fluorescent screen comprises a dispersion of fluorescent particles in a resin binder. Due to the rather high dielectric properties of the binder, the fluorescent screen also acts as an insulating layer between the support and photoconducting layer. As a consequence, when such a plate is exposed to an optical image, dissipation or conduction of the electric charges away from the exposed areas is hindered. However, such a double layer coating can be made to function efficiently by dispersing particles of the fluorescent material in a lower molecular weight aminoalochol described above. Since the fluorescent particles are dispersed in a conducting environment, electrophotographic recording elements embodying this feature allow for easy dissipation and removal of the electric charges with the subsequent production of electrophotographic prints and fog-free background.
In the accompanying drawing, FIGS. 1 and 2 represent sectional views of an electrophotographic member constructed in accordance with our invention.
In FIG. 1, a base plate 1. of paper has precoated thereon a layer 2 of an aminoalcohol described above which, in turn, is overlayed with a photoconductive insulating layer 3 comprising an electrical insulating binder 4 having dispersed therein particles of a photoconducting material 5.
In FIG. 2, 1 is a base or backing support; 6 represents a fluorescent layer comprising an aminoalcohol matrix 2 having imbedded or dispersed therein particles of a fluorescent material 7; and 3 is a photoconductive layer in which the photoconducting material 5 is dispersed or distributed throughout an electrically insulating binder 4.
Examples of photoconductors which we can employ for the purpose described herein include zinc oxide, sulfur, anthracene, anthraq-uinone, lead oxide, lead iodide, cadmium sulfide, cadmium selenide and the like.
In some instances, it may be desirable to incorporate sensitizing dyes in electrostatic recording elements in order to alter the spectral response of a particular photoconductive material. Thus, a sensitizing dye may be selected for the purpose of increasing the speed of the spectral response of a photoconductive material by extending or increasing the characteristic or inherent absorption of the photoconducting material itself. Or, a dye may be selected for the purpose of sensitizing the photoconducting material to a different portion of the spectrum and thus extend the band of frequencies to which the photoconducting material will respond. Among the dyes which have been suggested as sensitizers for use in electrophotography are the phthalein type dyes such as rose bengal, the triphenylmethane dyes such as malachite green and methyl green, the cyanine dyes such as kryptocyanine, acridine orange as well as many others.
It has been our observation that the electrical conductivity of the backing plate or support, after treatment with an aminoalcohol of the type described above, should have about the same value or higher as that of the photoconductor under the influence of the exciting radiation. However, regardless of the theory, the fact remains that a nonmetallic base plate treated in the above manner results in an electrophotographic recording member which yields images having little or no fogged backgrounds.
A coating composition containing one of the aforesaid aminoalcohols is prepared by dissolving the appropriate aminoalcohol in a suitable solvent and the resulting mixture coated on a non-metallic base of the type previously described. In some instances, it may be desirable to add various adjuncts to the composition in order to facilitate the coating operation. To this end, mention may be made of incorporating various dispersions of wax or wax-like materials, the function of which is to retard slippage by reducing the coefiicient of friction when such coatings are wound on magazines or spools. It may also be desirable to add spreading agents to the coating compositions, the purpose of which is to effect even distribution of the coating compositions on the base or support in order that the layers of uniform thickness will ensue.
In the interest of uniformity, all coatings were made on paper and all the electrical measurements were carried out under identical conditions of temperature, humidity and illumination.
The invention is illustrated by the following examples. It is to be understood, however, that no limitations are placed on the invention by such examples.
Example 1 A paper base having a resistivity of 1.5 l ohms centimeter was coated with the following composition: An aminoalcohol of the type described above g Toluene ml and then allowed to dry.
A second coating consisting of a dispersion of a photoconductor in a binder was prepared as follows: 20 g. of zinc oxide, 16 g. of silicone resin and 20 g. of toluene were placed in a porcelain ball-mill of one quart capacity half filled with 0.5 in. porcelainb'alls and milled for about two hours. The mixture was then coated by applicator roller method on the above subbed paper base and allowed to dry. The thickness of the photo-conductive layer was about 10 microns. An electrostatic charge was placed on the plate and exposed to radiation to effect discharge of the plate. The residual surface charge was then measured using a dynamic electrometer. A second electrophotographic plate was prepared as above except the paper base was not treated with the aminoalcohol. On charging and exposing, the residual surface charge on the second plate was much higher than in the case of the first plate.
As a consequence of the low residual surface charge remaining on the electrophotographic member having the base treated as above, the resulting prints obtained therefrom are free of background fog.
The silicone resin was obtained on the commercial market as GE Silicone Resin SR-82, a product of the General Electric Company, Pittsfield, Mass.
The zinc oxide photoconductor was purchased commercially as French Process Florence Green Seal Pigment Grade, 2. product of the New Jersey Zinc Sales Company, Inc., New York, New York.
Example 2 The same procedure was followed as given in Example 1 excepting that the zinc oxide photoconductor was sensitized to the green portion of the spectrum with rose bengal dye. 0.01 gram of sensitizer was added to the zinc oxide dispersion during the ball-milling stage.
Example 3 15 grams of zinc sulfide (copper and cobalt activated) and 20 g. of the aminoalcohol solution of Example 1 was ball-milled for two hours. The resulting dispersion of fluorescent agent was then coated on a metal base using the applicator roller method. The thickness of the layer amounted to about 10 microns. A photoconductive layer of the type described in Example 2 was next applied over the first layer and allowed to dry. The resulting electrophotographic recording element containing an intermediate fluorescent layer interposed between the base and photoconductive layer is particularly valuable in the field of radiography wherein the exciting radiation are X-rays. In operation, the element is first electrostatically charged in the usual manner and then exposed to an X-ray pattern or image. At the exposed areas, the electrostatic charges comprising the latent image are neutralized. In addition to the direct discharge of the latent image, the X-rays cause the fluorescent layer to emit light which neutralizes more of the electrostatic charges. Thus, the combination of a fluorescent substance and photoconductor operate in a synergistic manner to increase the efliciency of the system.
Example 4 The same procedure was employed as given in Example 3 excepting that the metal base was replaced by a paper base. I
We claim:
.1. The article as defined in claim 9 wherein the photoconductor is dye sensitized.
2. The article as defined in claim 10 wherein the fluorescent material is selected from the class consisting of copper activated zinc sulfide, copper and cobalt acti- Vated zinc sulfide, silver activated zinc sulfide, zinc cadmium sulfide, magnesium titanium dioxide, calcium tungstate and cesium halide.
3. The articleas defined in claim 9 wherein the electrically insulating binder is a silicone resin.
4. The article as defined in claim 2. wherein the fluorescent material is copper cobalt activated zinc sulfide.
5. The article as defined in claim 9 wherein the base is paper.
6. The process as defined in claim 11 wherein the exposing radiation are X-rays.
7. An electrophotographic member as recited in claim 9 wherein said insulating film-forming binder has an electrical resistance of about 10 to 10 ohm centimeter.
8. An electrophotographic process as recited in claim 11 wherein the electrically insulating film-forming binder has an electrical resistivity of about 10 to 10 ohm centimeter.
9. An electrophotographic member comprising a nonmetallic base plate of high electrical resistance, a coating on said base plate for increasing the electrical conductivity of the plate, said coating comprising an aminoalcohol selected from the group consisting of Z-amino-I-butanol, 2-amino-2-methyl-l-propanol, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-ethyl-1,3-propanediol, tris(hy-droxymethyl)aminomethane, 2-amino-2-methyl-1-butanol, 2- amino-l-ethanol, 3-amino-2,3-dimethyl-2-butanol, l-amino-2-methyl-2-butanol, 1-amino-3-methyl-2-butanol, 2- amino-l-propanol, l-amino-2-methyl-2-propanol, Z-aminol-pentanol, 3-amino-1,2-pentanol and 2-amino-2-methyl- 3-pentanol; said coating covered by a layer comprising a photoconductive zinc oxide uniformly dispersed in an insulating film-forming binder having an electrical resistance higher than that of the base plate on said coated base plate.
10. An electrophotographic member comprising a nonmetallic base plate of high electrical resistivity, an intermediate fluorescent layer bonded to said plate and an upper layer comprising a zinc oxide photoconductor uniformly dispersed in an electrically insulating filmforming binder having an electrical resistance higher than that of the base plate and photoconductor, the fluorescent layer comprising a fluorescent material uniformly dispersed throughout an aminoalcohol selected from the group consisting of 2-amino-l-butanol, 2-amino-2-methyll-propanol, Z-amino-Z-methyl-1,3-propanediol, Z-amino- 2 ethyl-1,3-propanediol, tris(hydroxymethyl)aminomethane, 2-amino-2-methyl-l-butanol, Z-amino-l-ethanol, 3- amino-Z,3-dimethyl-2-butanol, l-amino-Z-methyl-Z-butan01, 1-amino-3-methyl-2-butanol, Z-amino-l-propanol, 1- amino-2-methyl-2-propanol, 2-amino-l-pentanol, 3-amino- 1,2-pentanol and 2-amino-2-methyl-3-pentanol.
11. In an electrophotographic process comprising placing an electrostatic charge on the surface of an electrophotographic member comprising a non-metallic base plate, a layer thereon comprising a zinc oxide photoconductor uniformly dispersed in an electrically insulating film-forming binder having an electrical resistance higher than that of the base plate and photoconductor; selectively neutralizing the electrostatic charge from the surface of the charged photoconductive insulating layer by exposing said charged layer to radiation of a wave length ranging from 10- centimeters to 1O centimeters thereby creating an electrostatic latent image on the surface of the photoconducting insulating layer and developing said electrostatic latent image with electrically charged powder particles, the improvement of applying to the base plate in order to increase its electrical conductivity, an aminoalcohol selected from the group consisting of Z-amino-I-butanol, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1,3-propanediol, 2-amino-2-ethyl- 1,3-pr0panediol, tris(hydroxymethyl)aminomethane, 2- amino-Z-methyl-l-butanol, 2-amino-1-ethanol, 3-amino-2, 3-dimethy1-2-butanol, 1-amino-Z-methyl-Lbutanol, 1-amin0-3-methyl-2-butanol, 2-amin0-1-propanol,
1-amin0-2- methyl-Z-propanol, 2-amino-1-pentanol, 3-amino-1,2-pentanol and 2-amino-2-methy1-3-pentanol.
References Cited in the file of this patent UNITED STATES PATENTS Hartmann July 22,
8 Dessauer et a1. Aug. 25, 1959 Nan Dorn et a1. May 24, 1960 Tanenbaum Aug. 22, 1961 Kostelec Oct. 3, 1961 FOREIGN PATENTS Australia June 16, 1954 Australia Nov. 1, 1956 OTHER REFERENCES Young et al.: R.C.A. Review, volume XV, Number 4, pages 469-484 (December 1954).
Metcalfe et 31.: Journal of the Oil and Colour Chemists Association, volume 39, Number 11, pages 845-856
Claims (1)
- 9. AN ELECTROPHOTOGRAPHIC MEMBER COMPRISING A NONMETALLIC BASE PLATE OF HIGH ELECTRICAL RESISTANCE, A COATING ON SAID BASE PLATE FOR INCREASING THE ELECTRIAL CONDUCTIVITY OF THE PLATE, SAID COATING COMPRISING AN AMINOALCOHOL SELECTED FROM THE GROUP CONSISTING OF 2-AMINO-1-BUTANOL, 2-AMINO-2-METHYL-1-PROPANOL, 2-AMINO-2-METHYL-1,3-PROPANEDIOL, 2-AMINO-2-ETHYL-1,3-PROPANEDIOL, TRIS(HYDROXYMETHYL)AMINOMETHANE, 2-AMINO-2-METHYL-1-BUTANOL, 2AMINO-1-ETHANOL, 3-AMINO-2,3-DIMETHYL-2-BUTANOL, 1-AMINO-2-METHYL-2-BUTANOL, 1-AMINO-3-METHYL-2-BUTANOL, 2AMINO-1-PROPANOL, 1-AMINO-2-METHYL-2-PROPANOL, 2-AMINO1-PENTANOL, 3-AMINO-1,2-PENTANOL AND 2-AMINO-2-METHYL3-PENTANOL; SAID COATING COVERED BY A LAYER COMPRISING A PHOTOCONDUCTIVE ZINC OXIDE UNIFORMLY DISPERSED IN AN INSULATING FILM-FORMING BINDER HAVING AN ELECTRICAL RESISTANCE HIGHER THAN THAT OF THE BASE PLATE ON SAID COATED BASE PLATE.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US804411A US3095301A (en) | 1959-04-06 | 1959-04-06 | Electrophotographic element |
| DEA34369A DE1157478B (en) | 1959-04-06 | 1960-04-05 | Electrophotographic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US804411A US3095301A (en) | 1959-04-06 | 1959-04-06 | Electrophotographic element |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3095301A true US3095301A (en) | 1963-06-25 |
Family
ID=25188910
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US804411A Expired - Lifetime US3095301A (en) | 1959-04-06 | 1959-04-06 | Electrophotographic element |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3095301A (en) |
| DE (1) | DE1157478B (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3206600A (en) * | 1963-05-21 | 1965-09-14 | Keuffel & Esser Co | Image-formation on electro-photographic material |
| US3222986A (en) * | 1963-01-04 | 1965-12-14 | Altman Gerald | System of optical projection of images by reflex reflected illumination |
| US3398336A (en) * | 1965-05-17 | 1968-08-20 | Xerox Corp | Electrical charging utilizing a twophase liquid medium |
| US3403019A (en) * | 1965-02-15 | 1968-09-24 | Eastman Kodak Co | Photoconductive electrostatic elements containing polyurethanes in the photoconductive layer |
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| US2346670A (en) * | 1940-01-19 | 1944-04-18 | Western Union Telegraph Co | Method of and means for recording signals electrically |
| US2403533A (en) * | 1943-08-18 | 1946-07-09 | Gen Aniline & Film Corp | Nonstatic photographic film |
| US2772972A (en) * | 1954-08-20 | 1956-12-04 | Gen Aniline & Film Corp | Positive diazotype printing plates |
| US2774921A (en) * | 1953-04-23 | 1956-12-18 | Haloid Co | Apparatus for electrostatically charging insulating image surfaces for electrophotography |
| US2825814A (en) * | 1953-07-16 | 1958-03-04 | Haloid Co | Xerographic image formation |
| US2844734A (en) * | 1955-05-14 | 1958-07-22 | Hartmann Josef-Heinrich | Arrangement for producing plural photographic exposures |
| US2901348A (en) * | 1953-03-17 | 1959-08-25 | Haloid Xerox Inc | Radiation sensitive photoconductive member |
| US2937944A (en) * | 1957-11-20 | 1960-05-24 | Haloid Xerox Inc | Xerographic light-sensitive member and process therefor |
| US2997387A (en) * | 1957-12-17 | 1961-08-22 | Ozalid Co Ltd | Photographic reproduction |
| US3002835A (en) * | 1958-07-30 | 1961-10-03 | Gen Aniline & Film Corp | Photoconductive recording element |
-
1959
- 1959-04-06 US US804411A patent/US3095301A/en not_active Expired - Lifetime
-
1960
- 1960-04-05 DE DEA34369A patent/DE1157478B/en active Pending
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2346670A (en) * | 1940-01-19 | 1944-04-18 | Western Union Telegraph Co | Method of and means for recording signals electrically |
| US2403533A (en) * | 1943-08-18 | 1946-07-09 | Gen Aniline & Film Corp | Nonstatic photographic film |
| US2901348A (en) * | 1953-03-17 | 1959-08-25 | Haloid Xerox Inc | Radiation sensitive photoconductive member |
| US2774921A (en) * | 1953-04-23 | 1956-12-18 | Haloid Co | Apparatus for electrostatically charging insulating image surfaces for electrophotography |
| US2825814A (en) * | 1953-07-16 | 1958-03-04 | Haloid Co | Xerographic image formation |
| US2772972A (en) * | 1954-08-20 | 1956-12-04 | Gen Aniline & Film Corp | Positive diazotype printing plates |
| US2844734A (en) * | 1955-05-14 | 1958-07-22 | Hartmann Josef-Heinrich | Arrangement for producing plural photographic exposures |
| US2937944A (en) * | 1957-11-20 | 1960-05-24 | Haloid Xerox Inc | Xerographic light-sensitive member and process therefor |
| US2997387A (en) * | 1957-12-17 | 1961-08-22 | Ozalid Co Ltd | Photographic reproduction |
| US3002835A (en) * | 1958-07-30 | 1961-10-03 | Gen Aniline & Film Corp | Photoconductive recording element |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3222986A (en) * | 1963-01-04 | 1965-12-14 | Altman Gerald | System of optical projection of images by reflex reflected illumination |
| US3269839A (en) * | 1963-01-04 | 1966-08-30 | Altman Gerald | Photographic product for direct viewing and directive imaging |
| US3206600A (en) * | 1963-05-21 | 1965-09-14 | Keuffel & Esser Co | Image-formation on electro-photographic material |
| US3403019A (en) * | 1965-02-15 | 1968-09-24 | Eastman Kodak Co | Photoconductive electrostatic elements containing polyurethanes in the photoconductive layer |
| US3398336A (en) * | 1965-05-17 | 1968-08-20 | Xerox Corp | Electrical charging utilizing a twophase liquid medium |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1157478B (en) | 1963-11-14 |
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