US3490941A - Impregnated paper for reproduction processes - Google Patents
Impregnated paper for reproduction processes Download PDFInfo
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- US3490941A US3490941A US538410A US3490941DA US3490941A US 3490941 A US3490941 A US 3490941A US 538410 A US538410 A US 538410A US 3490941D A US3490941D A US 3490941DA US 3490941 A US3490941 A US 3490941A
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- recording sheet
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- 238000000034 method Methods 0.000 title description 24
- 230000008569 process Effects 0.000 title description 12
- 239000004065 semiconductor Substances 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 239000000463 material Substances 0.000 description 18
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical group O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 16
- 230000003197 catalytic effect Effects 0.000 description 15
- 239000000835 fiber Substances 0.000 description 13
- 238000007654 immersion Methods 0.000 description 12
- 239000002253 acid Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- DAMJCWMGELCIMI-UHFFFAOYSA-N benzyl n-(2-oxopyrrolidin-3-yl)carbamate Chemical compound C=1C=CC=CC=1COC(=O)NC1CCNC1=O DAMJCWMGELCIMI-UHFFFAOYSA-N 0.000 description 9
- WMWLMWRWZQELOS-UHFFFAOYSA-N bismuth(III) oxide Inorganic materials O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 7
- 239000000908 ammonium hydroxide Substances 0.000 description 7
- 239000002019 doping agent Substances 0.000 description 7
- 239000000123 paper Substances 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- JHXKRIRFYBPWGE-UHFFFAOYSA-K bismuth chloride Chemical compound Cl[Bi](Cl)Cl JHXKRIRFYBPWGE-UHFFFAOYSA-K 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 5
- 230000001476 alcoholic effect Effects 0.000 description 5
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 229910000365 copper sulfate Inorganic materials 0.000 description 4
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 4
- 230000005684 electric field Effects 0.000 description 4
- 239000003906 humectant Substances 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- LIYKJALVRPGQTR-UHFFFAOYSA-M oxostibanylium;chloride Chemical compound [Cl-].[Sb+]=O LIYKJALVRPGQTR-UHFFFAOYSA-M 0.000 description 3
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229940007424 antimony trisulfide Drugs 0.000 description 1
- NVWBARWTDVQPJD-UHFFFAOYSA-N antimony(3+);trisulfide Chemical compound [S-2].[S-2].[S-2].[Sb+3].[Sb+3] NVWBARWTDVQPJD-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 229940073609 bismuth oxychloride Drugs 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- PDZKZMQQDCHTNF-UHFFFAOYSA-M copper(1+);thiocyanate Chemical compound [Cu+].[S-]C#N PDZKZMQQDCHTNF-UHFFFAOYSA-M 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000007420 reactivation Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/20—Duplicating or marking methods; Sheet materials for use therein using electric current
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/705—Compositions containing chalcogenides, metals or alloys thereof, as photosensitive substances, e.g. photodope systems
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G17/00—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process
- G03G17/02—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process with electrolytic development
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G17/00—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process
- G03G17/04—Electrographic processes using patterns other than charge patterns, e.g. an electric conductivity pattern; Processes involving a migration, e.g. photoelectrophoresis, photoelectrosolography; Processes involving a selective transfer, e.g. electrophoto-adhesive processes; Apparatus essentially involving a single such process using photoelectrophoresis
-
- 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
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
Definitions
- the present invention relates to a novel electro-sensitive paper. More particularly, the invention relates to an electro-sensitive recording sheet which does not contain or require a distinct electrically conductive backing layer.
- Electro-sensitive recording sheets heretofore known generally comprised an electrically conductive backing and a contiguous layer of a suitable electro-sensitive material.
- the electrically conductive backings that have been employed in the art include metal foil, paper or fabric impregnated with conductive particles such as aluminum fiakes, vapor deposited metal filnis, conductive plastics, etc.
- the contiguous electro-sensitive layer usually comprises a dispersion of electro-sensitive material in a binder having a low electrical conductivity.
- an electro-photographic sandwich structure consisting of, in the order named, an electrode which may be formed of conductive glass, a photoconductive layer which may be formed of cadmium selenide, zinc oxide or antimony trisulfide, a catalyst layer which acts as a source of catalytic ions, a recording layer comprising a semiconductor material, and a conductive backing for the material.
- a suggested conductive backing, which functions as an electrode, is aluminum foil.
- a positive-to-positive reproduction system According to the invention disclosed therein, a substantially permanent positive image is formed by having an image projected onto a catalytic layer supported on a conductive backing and then placing the catalytic layer in contact with a copy sheet comprising a semiconductor oxide supported on an electrically conductive backing and applying an electric field between the conductive base of the catalytic layer and the conductive base of the copy sheet.
- Another object of this invention is to provide a copy sheet which can be employed in the reproduction processes ice disclosed in my aforementioned co-pending applications as well as in other prior art reproduction processes employing sensitive materials heretofore deposited on an electrically conductive backing.
- a still further object of the present invention is to provide methods for producing the electro-sensitive recording sheet of the present invention.
- the figure is a schematic diagram of a photocopy apparatus that employs the electro-sensitive copy sheet of the present invention.
- an electro-sensitive recording sheet which does not require the presence of an electrically conductiv backing layer. It has been found that electro-sensitive materials can be uniformly precipitated inside of the fibers of a suitable recording sheet.
- the electro-sensitive materials comprise those materials known in the art such as semiconductor oxides. These oxides are known as materials suitable for use in electro-sensitive paper because they undergo a change in color upon reduction to a lower oxidation state.
- the process of the present invention results in the precipitation of a suitable oxide pigment inside the fibers of the recording sheet.
- the oxide pigment introduced according to the process of the present invention is evenly distributed throughout the recording sheet.
- the electro-sensitiv material is doped to bring out the semiconductive properties of the material.
- the doping material and procedure will vary somewhat with the semiconductor material considered, as will be understood by those skilled in the art.
- An electro-sensitive material which has been found particularly suitable is antimony trioxide.
- This oxide results in a recording sheet which can be employed Without any electrically conductive backing layer.
- One manner of preparing a recording sheet containing antimony trioxide inside the fibers is by passing an untreated recording sheet into a bath comprising an acid solution of an antimony trihalide (such as antimony trichloride) in hydrochloric acid. After the recording sheet has been thoroughly soaked in the solution of antimony trichloride, the sheet is transferred to another bath containing cool running water (a temperature of 15 C. is suitable).
- an aqueous ammonium hydroxide bath can alternatively be employed to bring about precipitation on the recording sheet.
- the antimony oxychloride which covers the surface of the recording sheet is converted into the corresponding oxide by imersing the recording sheet in water, preferably boiling water.
- the oxychloride precipitate is converted into oxide according to the following equation:
- the antimony trioxide pigment is formed inside of the fibers of the recording sheet.
- the semiconductive properties are brought out by doping the oxide.
- the doping material and procedure is determined from the semiconductors energy band structure and solid state properties.
- a solution of copper sulfate may be employed to dope the crystal.
- the doping of the oxide can be simply accomplished by immersing the recording sheet in a solution of a suitable doping agent.
- the recording sheet is dried by suitable means known in the art, such as, for example, under tension between two layers of blotting paper. This avoids wrinkling of the recording sheet.
- a recording sheet containing antimony trioxide uniformly distributed inside the fibers of the sheet may be prepared by passing the untreated sheet into a bath comprising an alcohol (e.g. methanol) solution of antimony trichloride. After the recording sheet has been thoroughly soaked in the alcoholic solution of antimony trichloride, the sheet is transferred to a bath containing cool water. This transfer to a water bath results in the precipitation of antimony oxychloride which covers the surface of the recording sheet. The precipitation can also be effected by employing an aqueous ammonium hydroxide bath in place of the water bath. The precipitate on the recording sheet is then converted to the corresponding oxide in the manner described above.
- an alcohol e.g. methanol
- Another semiconductor oxide that can be precipitated inside the fibers of a recording sheet and eliminates the necessity of having an electrically conductive base layer is bismuth trioxide.
- the processes described above for the introduction of antimony trioxide inside the fibers of a recording sheet are the same for bismuth trioxide.
- the bismuth trioxide is introduced inside the fibers of the recording sheet by first immersing the untreated sheet in an acid solution of bismuth trichloride in hydrochloric acid. After the recording sheet has been immersed in the acid solution, it is immersed in a bath of cool water. This immersion results in the formation of a preciptate of bismuth oxychloride on the surface of the recording sheet. The formation of this precipitate upon the immersion of the sheet in the water bath is shown by the following equations:
- the doping of the sheet containing bismuth trioxide inside the fibers is performed by immersion of the sheet in a doping solution containing a suitable doping agent.
- the doping solution comprises an ionic salt such as ammonium nitrate in water, a minor amount of humectant such as glycerol, sorbitol or other glycol and the desired doping material, in this case, nickel chloride.
- EXAMPLE 1 A paper to be used as an electro-sensitive recording sheet was soaked for about one minute in an acid solution comprising 100 grams bismuth trichloride in 100 cc. 37% hydrochloric acid and 100 cc. water. After immersion in the acid solution of bismuth trichloride, the sheet is transferred to another solution comprising 70 cc. of ammonium hydroxide in 200 cc. water and immersed in that solution for about ten minutes while agitating the solution.
- the semiconductive properties of the bismuth trioxide are brought out by immersing the sheet, wth agitation for ten minutes, in a solution comprising 0.6 gram nickel chloride, 160 grams ammonium nitrate, 25 cc. glycerol and 380 cc. of water. After immersion in the doping solution the sheet is dried between blotters.
- EXAMPLE 2 A recording sheet was prepared according to Example 1, except that the untreated sheet was immersed in an alcoholic solution comprising grams bismuth trichloride and 300 cc. methanol for about five minutes in place of the acid solution of Example 1.
- EXAMPLE 3 A recording sheet was prepared according to Example 1, except that precipitation was brought about by immersion of the sheet in a distilled cool water bath in place of the aqueous ammonium hydroxide solution of that example.
- EXAMPLE 4 A recording sheet was prepared according to Example 1, except that antimony trichloride was used in place of bismuth trichloride and the doping material was 0.5 gram of copper sulfate instead of the nickel chloride of that example.
- the semiconductor oxide recording sheet of the present invention which does not contain an electrically conductive backing layer, is particularly useful in photocopy applications, and may be utilized in an apparatus such as that illustrated in the drawing, for example.
- Photocopy apparatus 10 comprises a lens 11 for focussing an image of a document 12, or other subject to be reproduced.
- the image of a document is focussed by lens 11 under illumination from light sources 13 and 14 on to a catalytic belt 15.
- the composition used for the catalytic belt 15 can be a mixture of a metal thiocyanate with an oxide capable of being reduced to a lower state of oxidation.
- a preferred catalytic composition includes a mixture of cuprous thiocyanate with titanium dioxide.
- the catalytic belt 15 is driven by rollers 16 and 17.
- These rollers 17 and 19 are electrically connected by leads 20 and 21 to a source of electrical potential 22 providing the necessary electrical field for the transfer of the latent image formed on the catalytic belt 15 onto the copy sheet 18.
- the positive reproduction 23 of the original image is transferred outside the machine by belt 24 driven by pulleys 25 and 26.
- the latent image on the catalytic belt 15 can be erased by providing an electrical potential between rollers 16 and '26 which are connected by leads 27 and 28 to a source of electrical potential 29.
- the image is erased due to the reactivation of the deactivated catalyst in the catalytic belt 15.
- the electric field applied between roller 26 and the base of the catalytic belt causes electrons to be accepted by the neutralized metal ions in the belt and, therefore, reinstates the original ionic nature of the catalytic surface so that it can be used continuously.
- the electro-sensitive recording sheet of the present invention can also effectively be employed in the photocopy processes of my copending application Ser. Nos. 487,480 now abandoned and 491,786 now U.S. Patent 3,309,198, filed Sept. 15, 1965 and Sept. 30, 1965, respectively.
- the disclosure of U.S. Patent 3,309,198 is incorporated herein by reference, particularly as to the semiconductor oxides disclosed therein.
- the copysheet of the present invention may be utilized in numerous reproduction processes of the prior art which employ semiconductor oxides.
- a recording sheet consisting essentially of a semiconductor oxide selected from the class consisting of antimony trioxide and bismuth trioxide, said semiconductor oxide being impregnated into the fibers of said medium, said medium being free of any electrically conductive backing layer and said semiconductor oxide being in a higher state of oxidation and undergoing a change in color upon reduction to a lower oxidation state.
- a copy sheet according to claim 3 wherein the semiconductor oxide is antimony trioxide.
- a copy sheet according to claim 4 wherein said doping composition comprises a doping agent of copper sulfate in a solution of an ionic salt and a humectant.
- a copy sheet according to claim 3 wherein the semi conductor oxide is bismuth trioxide.
- said doping composition comprises a doping agent of nickel chloride in a solution of an ionic salt and a humectant.
- the method of preparing a semiconductor oxide recording sheet which does not contain any electrically conductive backing layer which comprises immersing an untreated sheet in an acid solution or an alcoholic solution containing a corresponding halide of the semiconductor oxide to be impregnated inside of the fibers of said recording sheet subsequently, immersing said sheet in a medium selected from the class consisting of water and an aqueous ammonium hydroxide solution, thereby forming a precipitate on said recording sheet, immersing said recording sheet in boiling Water to convert said precipitate to the semiconductor oxide and drying said recording sheet.
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Description
0 7 I J. J. A. ROIBILLARD 3,490,941
IMPREGNATED PAPER FOR REPRODUCTION PROCESSES Filed March 29, 1966 INVENTOR. JEAN J. A. ROBILLARD ATTORNEYS United States Patent IMPREGNATED PAPER FOR REPRODUCTION PROCESSES Jean J. A. Robillard, Zumikon, Zurich, Switzerland, as-
signor to US. Philips Corporation, New York, N.Y., a corporation of Delaware Filed Mar. 29, 1966, Ser; No. 538,410 Int. Cl. G03g 5/00; D21h 1/02 US. Cl. 117-201 14 Claims ABSTRACT OF THE DISCLOSURE A copy sheet impregnated with a semiconductor oxide and having no electrically conductive backing is described. The copy sheet is prepared by forming a precipitate on the recording surface and subsequently converting the precipitate to the oxide by immersion of the sheet in boiling water.
The present invention relates to a novel electro-sensitive paper. More particularly, the invention relates to an electro-sensitive recording sheet which does not contain or require a distinct electrically conductive backing layer.
Electro-sensitive recording sheets heretofore known generally comprised an electrically conductive backing and a contiguous layer of a suitable electro-sensitive material. The electrically conductive backings that have been employed in the art include metal foil, paper or fabric impregnated with conductive particles such as aluminum fiakes, vapor deposited metal filnis, conductive plastics, etc. The contiguous electro-sensitive layer usually comprises a dispersion of electro-sensitive material in a binder having a low electrical conductivity.
In my copending US. patent application Ser. No. 205,600 filed June 27, 1962 and now Patent No. 3,355,290, there is disclosed a reproductionprocess for the introduction of avsmall amount of catalyst ions into a semiconductor layer under the application of an electric field. The introduction of the catalyst ions into the semiconductor layer provides a stable, high contrast record of an original image projected onto the recording structure. There is disclosed, as an embodiment of the invention set forth therein, an electro-photographic sandwich structure consisting of, in the order named, an electrode which may be formed of conductive glass, a photoconductive layer which may be formed of cadmium selenide, zinc oxide or antimony trisulfide, a catalyst layer which acts as a source of catalytic ions, a recording layer comprising a semiconductor material, and a conductive backing for the material. A suggested conductive backing, which functions as an electrode, is aluminum foil.
Also in my co-pending application Ser. No. 463,841 filed June 14, 1965, there is disclosed a positive-to-positive reproduction system. According to the invention disclosed therein, a substantially permanent positive image is formed by having an image projected onto a catalytic layer supported on a conductive backing and then placing the catalytic layer in contact with a copy sheet comprising a semiconductor oxide supported on an electrically conductive backing and applying an electric field between the conductive base of the catalytic layer and the conductive base of the copy sheet.
It is an object of the present invention to provide a recording medium such as a copy sheet which does not require the use of a conductive backing such as aluminum foil, or the like. a
It is another object of th invention to provide an electrosensitive copy sheet capable of reproducing highly stable images with good definition and high contrast.
Another object of this invention is to provide a copy sheet which can be employed in the reproduction processes ice disclosed in my aforementioned co-pending applications as well as in other prior art reproduction processes employing sensitive materials heretofore deposited on an electrically conductive backing.
A still further object of the present invention is to provide methods for producing the electro-sensitive recording sheet of the present invention.
Other objects and advantages of th present invention will become apparent from the consideration of the following description in conjunction with the appended drawing.
The figure, is a schematic diagram of a photocopy apparatus that employs the electro-sensitive copy sheet of the present invention.
According to the present invention an electro-sensitive recording sheet is obtained which does not require the presence of an electrically conductiv backing layer. It has been found that electro-sensitive materials can be uniformly precipitated inside of the fibers of a suitable recording sheet. The electro-sensitive materials comprise those materials known in the art such as semiconductor oxides. These oxides are known as materials suitable for use in electro-sensitive paper because they undergo a change in color upon reduction to a lower oxidation state.
The process of the present invention results in the precipitation of a suitable oxide pigment inside the fibers of the recording sheet. The oxide pigment introduced according to the process of the present invention is evenly distributed throughout the recording sheet. After the pigment has been introduced in the manner to be described below, the electro-sensitiv material is doped to bring out the semiconductive properties of the material. The doping material and procedure will vary somewhat with the semiconductor material considered, as will be understood by those skilled in the art.
An electro-sensitive material which has been found particularly suitable is antimony trioxide. This oxide results in a recording sheet which can be employed Without any electrically conductive backing layer. One manner of preparing a recording sheet containing antimony trioxide inside the fibers is by passing an untreated recording sheet into a bath comprising an acid solution of an antimony trihalide (such as antimony trichloride) in hydrochloric acid. After the recording sheet has been thoroughly soaked in the solution of antimony trichloride, the sheet is transferred to another bath containing cool running water (a temperature of 15 C. is suitable). Upon transfer of the sheet from the acid solution of antimony trichloride to the bath containing cool water, a white precipitate of antimony oxychloride is formed which covers the surface of the recording sheet. The formation of this precipitate is due to the hydrolysis of the antimony trichloride according to the following equations:
If desired, an aqueous ammonium hydroxide bath can alternatively be employed to bring about precipitation on the recording sheet. The antimony oxychloride which covers the surface of the recording sheet is converted into the corresponding oxide by imersing the recording sheet in water, preferably boiling water. The oxychloride precipitate is converted into oxide according to the following equation:
As a result of this precipitation technique, the antimony trioxide pigment is formed inside of the fibers of the recording sheet. After the oxide has been formed in the sheet the semiconductive properties are brought out by doping the oxide. The doping material and procedure is determined from the semiconductors energy band structure and solid state properties. In the case of antimony trioxide, a solution of copper sulfate may be employed to dope the crystal. The doping of the oxide can be simply accomplished by immersing the recording sheet in a solution of a suitable doping agent. After the oxide has been doped, the recording sheet is dried by suitable means known in the art, such as, for example, under tension between two layers of blotting paper. This avoids wrinkling of the recording sheet.
Alternatively, a recording sheet containing antimony trioxide uniformly distributed inside the fibers of the sheet may be prepared by passing the untreated sheet into a bath comprising an alcohol (e.g. methanol) solution of antimony trichloride. After the recording sheet has been thoroughly soaked in the alcoholic solution of antimony trichloride, the sheet is transferred to a bath containing cool water. This transfer to a water bath results in the precipitation of antimony oxychloride which covers the surface of the recording sheet. The precipitation can also be effected by employing an aqueous ammonium hydroxide bath in place of the water bath. The precipitate on the recording sheet is then converted to the corresponding oxide in the manner described above.
Another semiconductor oxide that can be precipitated inside the fibers of a recording sheet and eliminates the necessity of having an electrically conductive base layer is bismuth trioxide. The processes described above for the introduction of antimony trioxide inside the fibers of a recording sheet are the same for bismuth trioxide.
For example, the bismuth trioxide is introduced inside the fibers of the recording sheet by first immersing the untreated sheet in an acid solution of bismuth trichloride in hydrochloric acid. After the recording sheet has been immersed in the acid solution, it is immersed in a bath of cool water. This immersion results in the formation of a preciptate of bismuth oxychloride on the surface of the recording sheet. The formation of this precipitate upon the immersion of the sheet in the water bath is shown by the following equations:
The conversion of the oxychloride into the corresponding oxide takes place in the same way as for antimony in a subsequent immersion in boiling water.
The doping of the sheet containing bismuth trioxide inside the fibers is performed by immersion of the sheet in a doping solution containing a suitable doping agent. The doping solution comprises an ionic salt such as ammonium nitrate in water, a minor amount of humectant such as glycerol, sorbitol or other glycol and the desired doping material, in this case, nickel chloride.
Specific illustrative but non-limiting examples of the preparation of the recording medium of the present invention are as follows:
EXAMPLE 1 A paper to be used as an electro-sensitive recording sheet was soaked for about one minute in an acid solution comprising 100 grams bismuth trichloride in 100 cc. 37% hydrochloric acid and 100 cc. water. After immersion in the acid solution of bismuth trichloride, the sheet is transferred to another solution comprising 70 cc. of ammonium hydroxide in 200 cc. water and immersed in that solution for about ten minutes while agitating the solution.
After about ten minutes immersion in the aqueous ammonium hydroxide solution the sheet was removed and washed with boiling water which resulted in precipitation of bismuth trioxide inside the fibers of the sheet.
The semiconductive properties of the bismuth trioxide are brought out by immersing the sheet, wth agitation for ten minutes, in a solution comprising 0.6 gram nickel chloride, 160 grams ammonium nitrate, 25 cc. glycerol and 380 cc. of water. After immersion in the doping solution the sheet is dried between blotters.
A recording of a 60 cycle per second electrical signal on the bismuth trioxide sheet was obtained.
EXAMPLE 2 A recording sheet was prepared according to Example 1, except that the untreated sheet was immersed in an alcoholic solution comprising grams bismuth trichloride and 300 cc. methanol for about five minutes in place of the acid solution of Example 1.
EXAMPLE 3 A recording sheet was prepared according to Example 1, except that precipitation was brought about by immersion of the sheet in a distilled cool water bath in place of the aqueous ammonium hydroxide solution of that example.
EXAMPLE 4 A recording sheet was prepared according to Example 1, except that antimony trichloride was used in place of bismuth trichloride and the doping material was 0.5 gram of copper sulfate instead of the nickel chloride of that example.
While the examples are given in specific quantities, it will be appreciated that in practice the total quantities may be adjusted to be appropriate for the processing apparatus. Unless otherwise indicated the process steps are conducted at room temperature approximately.
The semiconductor oxide recording sheet of the present invention which does not contain an electrically conductive backing layer, is particularly useful in photocopy applications, and may be utilized in an apparatus such as that illustrated in the drawing, for example.
The catalytic belt 15 is driven by rollers 16 and 17. The copy sheet 18, which is the electro-sensitive recording sheet of the present invention impregnated with a semiconductor oxide in a higher state of oxidation, and which does not contain an electrically conductive backing, is contacted with the catalytic belt 15 under the pressure of rollers 17 and 19. These rollers 17 and 19 are electrically connected by leads 20 and 21 to a source of electrical potential 22 providing the necessary electrical field for the transfer of the latent image formed on the catalytic belt 15 onto the copy sheet 18.
The positive reproduction 23 of the original image is transferred outside the machine by belt 24 driven by pulleys 25 and 26.
The latent image on the catalytic belt 15 can be erased by providing an electrical potential between rollers 16 and '26 which are connected by leads 27 and 28 to a source of electrical potential 29. The image is erased due to the reactivation of the deactivated catalyst in the catalytic belt 15. The electric field applied between roller 26 and the base of the catalytic belt causes electrons to be accepted by the neutralized metal ions in the belt and, therefore, reinstates the original ionic nature of the catalytic surface so that it can be used continuously.
The electro-sensitive recording sheet of the present invention can also effectively be employed in the photocopy processes of my copending application Ser. Nos. 487,480 now abandoned and 491,786 now U.S. Patent 3,309,198, filed Sept. 15, 1965 and Sept. 30, 1965, respectively. The disclosure of U.S. Patent 3,309,198 is incorporated herein by reference, particularly as to the semiconductor oxides disclosed therein. Furthermore, the copysheet of the present invention may be utilized in numerous reproduction processes of the prior art which employ semiconductor oxides.
Other variations and modifications of the present invention are possible and will be apparent to those of skill in the art. For example, the processes described above for the impregnation of the copysheet may be used to impregnate zinc oxide or equivalent materials to make a Xerographic paper for a process of the Electrofax type.
It is accordingly desired that the scope of the invention not be limited to those embodiments specifically illustrated or suggested, but that the scope of the invention be defined by reference to the appended claims.
What is claimed is:
1. A recording sheet consisting essentially of a semiconductor oxide selected from the class consisting of antimony trioxide and bismuth trioxide, said semiconductor oxide being impregnated into the fibers of said medium, said medium being free of any electrically conductive backing layer and said semiconductor oxide being in a higher state of oxidation and undergoing a change in color upon reduction to a lower oxidation state.
2. A recording medium according to claim 1 wherein said medium is a copy sheet.
3. A copy sheet according to claim 1 wherein the semiconductor oxide impregnated in the fibers of said copy sheet is doped with a doping composition.
4. A copy sheet according to claim 3 wherein the semiconductor oxide is antimony trioxide.
5. A copy sheet according to claim 4 wherein said doping composition comprises a doping agent of copper sulfate in a solution of an ionic salt and a humectant.
6. A copy sheet according to claim 3 wherein the semi conductor oxide is bismuth trioxide.
7. A copy sheet according to claim 6 wherein said doping composition comprises a doping agent of nickel chloride in a solution of an ionic salt and a humectant.
8. The method of preparing a semiconductor oxide recording sheet which does not contain any electrically conductive backing layer which comprises immersing an untreated sheet in an acid solution or an alcoholic solution containing a corresponding halide of the semiconductor oxide to be impregnated inside of the fibers of said recording sheet subsequently, immersing said sheet in a medium selected from the class consisting of water and an aqueous ammonium hydroxide solution, thereby forming a precipitate on said recording sheet, immersing said recording sheet in boiling Water to convert said precipitate to the semiconductor oxide and drying said recording sheet.
9. The method according to claim 8 wherein said untreated sheet is immersed in an acid solution or an alcoholic solution containing a member selected from the class consisting of antimony trichloride and bismuth trichloride.
10. The method according to claim 9, including the additional step of immersing said sheet in a doping composition comprising a doping agent in a solution of an ionic salt and a humectant, subsequent to the immersion of said sheet in boiling water.
11. The method according to claim 10 wherein the untreated sheet is immersed in an hydrochloric acid solution containing antimony trichloride, and wherein after immersion of said sheet in said acid solution said sheet is immersed in an aqueous ammonium hydroxide solution.
12. The method according to claim 11 wherein the doping agent is copper sulfate.
13. The method according to claim 10 wherein the untreated sheet is immersed in methanol solution containing bismuth trichlorideand wherein after immersion of said recording sheet in said alcoholic solution, said sheet is immersed in a water bath.
14. The method according to claim 13 wherein the doping agent is nickel chloride.
References Cited UNITED STATES PATENTS 2,959,481 11/1960 Kucera 961 3,010,884 11/1961 Johnson et al. 117--201 X 3,245,833 4/1966 Trevoy 117-201 WILLIAM L. JARVIS, Primary Examiner
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53841066A | 1966-03-29 | 1966-03-29 | |
FR6939593A FR2067816A5 (en) | 1966-03-29 | 1969-11-18 | Semi-conductive oxide impregnated duplicating paper |
NL6918639A NL6918639A (en) | 1966-03-29 | 1969-12-12 | |
DE19702002148 DE2002148A1 (en) | 1966-03-29 | 1970-01-09 | Impregnated paper for reproduction processes |
Publications (1)
Publication Number | Publication Date |
---|---|
US3490941A true US3490941A (en) | 1970-01-20 |
Family
ID=27431009
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US538410A Expired - Lifetime US3490941A (en) | 1966-03-29 | 1966-03-29 | Impregnated paper for reproduction processes |
Country Status (4)
Country | Link |
---|---|
US (1) | US3490941A (en) |
DE (1) | DE2002148A1 (en) |
FR (1) | FR2067816A5 (en) |
NL (1) | NL6918639A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3914546A (en) * | 1968-02-05 | 1975-10-21 | Xerox Corp | Common path image exploring apparatus |
WO1981002139A1 (en) * | 1980-01-30 | 1981-08-06 | Aussedat Rey | Method and paper for electro-sensitive recording |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2959481A (en) * | 1958-12-18 | 1960-11-08 | Bruning Charles Co Inc | Electrophotographic recording member and process of producing same |
US3010884A (en) * | 1957-10-28 | 1961-11-28 | Minnesota Mining & Mfg | Electrophotosensitive copy-sheet |
US3245833A (en) * | 1964-04-20 | 1966-04-12 | Eastman Kodak Co | Electrically conductive coatings |
-
1966
- 1966-03-29 US US538410A patent/US3490941A/en not_active Expired - Lifetime
-
1969
- 1969-11-18 FR FR6939593A patent/FR2067816A5/en not_active Expired
- 1969-12-12 NL NL6918639A patent/NL6918639A/xx unknown
-
1970
- 1970-01-09 DE DE19702002148 patent/DE2002148A1/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3010884A (en) * | 1957-10-28 | 1961-11-28 | Minnesota Mining & Mfg | Electrophotosensitive copy-sheet |
US2959481A (en) * | 1958-12-18 | 1960-11-08 | Bruning Charles Co Inc | Electrophotographic recording member and process of producing same |
US3245833A (en) * | 1964-04-20 | 1966-04-12 | Eastman Kodak Co | Electrically conductive coatings |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3914546A (en) * | 1968-02-05 | 1975-10-21 | Xerox Corp | Common path image exploring apparatus |
WO1981002139A1 (en) * | 1980-01-30 | 1981-08-06 | Aussedat Rey | Method and paper for electro-sensitive recording |
Also Published As
Publication number | Publication date |
---|---|
FR2067816A5 (en) | 1971-08-20 |
DE2002148A1 (en) | 1971-07-29 |
NL6918639A (en) | 1971-06-15 |
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