US3566108A - Corona generating electrode structure for use in a xerographic charging method - Google Patents
Corona generating electrode structure for use in a xerographic charging method Download PDFInfo
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- US3566108A US3566108A US612124A US3566108DA US3566108A US 3566108 A US3566108 A US 3566108A US 612124 A US612124 A US 612124A US 3566108D A US3566108D A US 3566108DA US 3566108 A US3566108 A US 3566108A
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- 238000000034 method Methods 0.000 title claims description 15
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 27
- 238000000576 coating method Methods 0.000 claims description 17
- 239000011248 coating agent Substances 0.000 claims description 16
- 229910052697 platinum Inorganic materials 0.000 claims description 13
- 239000010453 quartz Substances 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000010935 stainless steel Substances 0.000 claims description 5
- 229910001220 stainless steel Inorganic materials 0.000 claims description 5
- 239000004020 conductor Substances 0.000 claims description 4
- 239000011810 insulating material Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 abstract description 15
- 239000000835 fiber Substances 0.000 description 9
- 238000005260 corrosion Methods 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 4
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 229910001260 Pt alloy Inorganic materials 0.000 description 3
- 239000000908 ammonium hydroxide Substances 0.000 description 3
- -1 copperggold Chemical compound 0.000 description 3
- 238000009713 electroplating Methods 0.000 description 3
- 239000000203 mixture Substances 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
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
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- 238000007796 conventional method Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- PXXKQOPKNFECSZ-UHFFFAOYSA-N platinum rhodium Chemical compound [Rh].[Pt] PXXKQOPKNFECSZ-UHFFFAOYSA-N 0.000 description 2
- HWLDNSXPUQTBOD-UHFFFAOYSA-N platinum-iridium alloy Chemical compound [Ir].[Pt] HWLDNSXPUQTBOD-UHFFFAOYSA-N 0.000 description 2
- 239000005297 pyrex Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 235000010344 sodium nitrate Nutrition 0.000 description 2
- 239000004317 sodium nitrate Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 1
- 235000018185 Betula X alpestris Nutrition 0.000 description 1
- 235000018212 Betula X uliginosa Nutrition 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 241000282832 Camelidae Species 0.000 description 1
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- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/02—Apparatus for electrographic processes using a charge pattern for laying down a uniform charge, e.g. for sensitising; Corona discharge devices
- G03G15/0291—Apparatus for electrographic processes using a charge pattern for laying down a uniform charge, e.g. for sensitising; Corona discharge devices corona discharge devices, e.g. wires, pointed electrodes, means for cleaning the corona discharge device
Definitions
- a corona generating article is coating a strand or bundle of at least partially conductive.
- ion charging generally, comprises the application of charge to the photoconductive insulating surface by mechanically passing'across the photosensitive surface a corona generating electrode maintained at a potential of several thousand volts, normally in the order of 3 about 7000 volts with respect to ground potential.
- corona generating devices have been known to fail in service for various reasons/For example, the potentials required for corona generation produce an ozone rich atmosphere which corrosively attacks the corona generating device. ln addition, it has heretofore been necessary to use very thin wires to provide intense corona at reasonable electrical potentials.
- corona wires customarily measure 0.002 inches in diameter.
- the wires are, therefore, also subject to neckdown failures caused by vibration.
- U.S. Pat. No. 3,233,l56 to Jarvis and Robinson shows other possible corona discharge devices, however, these are unnecessarily complex.
- the requirements for a corona wire therefore, are that it'be corrosion resistant and mechanically strong.
- corona generating devices made of platinum alloys for example, are comparatively resistant to an ozone richatmosphere, they lack the tensile strength required of corona wires.
- lt is another object of this invention to provide a comparatively mechanically strong, corrosion resistant corona discharge article.
- a corona discharge article comprising a core made of one or more thin wires, filamerits, or fibers, hereafter referred to as strands, overcoated with a conductive corrosion resistant material.
- the core provides mechanical strength and the coating provides the corrosion resistance required for corona discharge purposes.
- the multistrand corona discharge core may be larger than the usual 0.002 inch corona wire because the surface curvature of the strands control the intensity of the corona generated, that is, the smaller the surface curvature of the corona discharge device is the less voltage is required to establish a usable corona.
- a bundle of about 0.008 inches in diameter made up of about 200 individual strands, each strand measuring about 0.0004 inches in diameter may be used in place of a conventional 0.002 inch corona discharge wire.
- the 0.008v inch bundle operating at the same potential as a 0.002 inch wire under similar conditions charges the surface of an'insulator to about the same; potential.
- the multistrand core corona generating article is useful for either positive or negative charging as is disclosed in U.S. Pat. No.
- the preferred corona discharge device therefore, comprises a multistrand core of quartz fibers twisted together and overcoated with a thin electrically continuous film of platinum.
- the quartz provides the tensile strength required of corona discharge devices and the platinum provides inertness to an:ozone'rich atmosphere and goodconductivity.
- the heterogeneous system provides increased working strength due to even distribution of stress among the'quartz fibers resulting from the use of a comparatively soft matrix.
- insulating-surface is intended to include'insulating and photoconductive insulating surface materials and materials such as electrographic'recording dielectrics.
- I conductive, semiconductive, or insulating material may be used as the strand material.
- Typical materials include strands of .quartz,'tungsten, platinum, platinumalloys, such as platinum-iridium, platinum-rhodium, etc., stainless steel, ceramics, glass, silicon carbide, boron nitride, and mixtures thereof. .Quartz is preferred because of its high'tensile strength and chemical resistivity.
- the coating material may be of any suitable conductive material.
- Typical conductive metals are: aluminum, brass, cadmium, copperggold, magnesium, nickel, noble metals and their alloys such as, platinum, platinum alloys such as platinum-iridium, platinum-rhodium, palladium, iridium, rhodium, etc., silver, stainless steel, tin, tungsten, and mixtures thereof.
- Corrosion'resistant semiconductive materials may be used.
- Typical semiconductive coatings include tin oxide, indi um oxide, and siliconcarbide. Platinum is preferred because of its inertness toan ozone rich atmosphere and its relatively high conductivity.
- FlG. 1 is a cross-sectional end view of an embodiment of the corona discharge source of this invention.
- FIG 2 is a cross-sectional'end view of'apreferred embodiment of the corona discharge source of this invention.
- FIG 3 is anend sectional view schematically illustrating the operation of this invention.
- a single strand cores isovercoated with conductive material 7 to form corona discharge device 8.
- The-coating may be applied to the core by any conventional method such as painting, spraying, dipping, plating, bychemical reaction, or by vacuum deposition.
- coated core 8 will not exceed in diameter conventional corona discharge devices which conventionally measure about 0.002 inches in diameter.
- Core Srnay be either insulating or conducting.
- a core comprising a plurality of fine strands 10'are overcoatedwith conductive'material lZJ
- the strands 10 may be overcoated after they are twisted, woven, or placed together.
- Corona discharge device l4 may be larger than conventional corona discharge wires.
- the coating may be applied to the strands by any conventional method such as painting, spraying, dipping, plating, by chemical reaction, or by vacuum deposition. The allowable thickness of coating 12 depends on the number of strands in the core and on the diameter of strands 10.
- a very thin coating 12 is preferred because a thick coat would fill the spaces between the outer strands 10 of the bundle resulting in loss of the small diameter surface curvature.
- a core comprising 200 strands of 0.0004 inch diameter quartz should have a coating thickness in the range of 0.0000l inches to 0.00005 inches-
- P10 2 shows the overcoating to be a thin coating over the surface of the core, it is preferred to have the overcoating material penetrate to all parts of the core bundle.
- a core comprising about 200 quartz fibers twisted together, each fiber measuring approximately 0.0004 inches in diameter (available from Lamp Glass Department, General Electric), is coated with Hanovia Liquid Bright Platinum 040 (available from the Hanovia Liquid Gold Division, Engelhard Industries) by brushing with a camel's hair brushdipped in the platinum solution. Sufficient solution is brushed onto the core to insure penetration of the solution into the core. The coated core is then placed in an oven and cured at a temperature of 400 C. for 1 hour. The platinum compounds decompose leaving behind a coating of pure platinum. The coated core is then recoated by brushing again with the camels hair brush dipped in the platinum solution and again baked at 400 C. for l hour to insure electrical continuity of the coating. The coating measures approximately 0.00002 inches. The coated core is then used as a corona generating article as is shown in U.S. Pat. No. 2,777,957 to Walkup.
- EXAMPLE II A core comprising about 70 wound stainless steel wires each wire measuring approximately 4 microns in diameter (available from the Brunswick Corporation) is immersed in an electroplating bath comprising 13.4 ounces of ammonium nitrate, 1.3 ounces of sodium nitrate, 2.2 ounces of platinum diammino nitrate and 6.7 ounces of 28 percent ammonium hydroxide in solution in 1 gallon of water.
- the electroplating bath is prepared as follows: The platinum diammino nitrate is separately dissolved by heating it in a 5 percent ammonium hydroxide solution.
- the diammino salt is thereby changed into the tetrammino salt which is then added to the solution of ammonium nitrate, sodium nitrate and ammonium hydroxide in water. Electroplating is accomplished by applying a potential difference of about 4.5 volts until the coating measures approximately 0.00004 inches. The coated core is then used as a corona generating article.
- EXAMPLE ill The experiment of example I is repeated with the exception that after the coated core is cured for the first time it is electroplated as in example ll. The resulting coating measures approximately 0.00004 inches.
- EXAMPLE W A core comprising about 200 Pyrex fibers twisted together each fiber measuring approximately 0.0004 inches in diameter available from Corning Glass Works is coated with platinum as in example 1.
- EXAMPLE V A core comprising about 200 Pyrex fibers twisted together each fiber measuring approximately 0.0004 inches in diameter available from Corning Glass Works is coated as in example lll.
- the method of electrostatically charging a member which comprises placing said member in the corona discharge of a corona generating electrode comprising a core of at least two strands overcoated with an electrically continuous coating of a conductive material.
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- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- General Physics & Mathematics (AREA)
- Electrostatic Charge, Transfer And Separation In Electrography (AREA)
Abstract
A corona generating article is provided by overcoating a strand or bundle of strands with a material which is at least partially conductive.
Description
United States Patent John W. Weigl, West Webster; Richard J. Komp, Webster, N .Y. 612,124
Jan. 27, 1967 Feb. 23, 1971 Xerox Corporation Rochester, N.Y.
Inventors Appl. N 0. Filed Patented Assignee CORONA GENERATING ELECTRODE STRUCTURE FOR USE IN A XEROGRAPI-IIC CHARGING METHOD 5 Claims, 3 Drawing Figs.
US. Cl. 250/495, 313/354, 317/262, 355/17 Int. Cl G03g 13/00 [50] Field ofSearch 313/354;
Primary Examiner-James W. Lawrence Assistant Examiner-A. L, Birch Anorneys-Stanley Z. Cole and James J. Ralabate ABSTRACT: A corona generating article is coating a strand or bundle of at least partially conductive.
provided by overstrands with a material which is ll/I/I/III/II/II/II/I/II/I/II/I/[g PAINTER F5523 1971 v INVENTOR$ JOHN w WE/GL R/CHA RD KOMP ATTORNEY CORONA GENERATING ELECTRODE STRUCTURE FOR USE IN A XEROGRAPHIC CHARGING METHOD charge pattern otherwise known as an electrostatic latentimage. This electrostatic latent image then is capable of being utilized such as, for example, by the deposition of electroscopic material thereon to form a visible image.
Usually the order of procedure is .to sensitize the xerographic plate by'applying a uniform charge to the surface of the photoconductive member after which exposure is made. The art of sensitizing the photoconductive insulating member as employed in that Carlson patent has been a difficult and complex one. Normally sensitization may be accomplished by any of various means, such as, for example, frictional means as disclosed in that Carlson patent or ion charging means-as shown in U.S. Pat. No. 2,777,957 to Walkup. Frictional charging, however, was found to be difficult in operation and generally resulted in an uneven or irregular charge across the surface of the photoconductor. The charge was also found to be too weak and insufficiently reproducible for use in xerography. lon charging on the other hand, has been fou'ndto produce uniform and reproducible charges on the surface of the insulating member. Thus, ion charging, generally, comprises the application of charge to the photoconductive insulating surface by mechanically passing'across the photosensitive surface a corona generating electrode maintained at a potential of several thousand volts, normally in the order of 3 about 7000 volts with respect to ground potential. However, conventional corona generating devices have been known to fail in service for various reasons/For example, the potentials required for corona generation produce an ozone rich atmosphere which corrosively attacks the corona generating device. ln addition, it has heretofore been necessary to use very thin wires to provide intense corona at reasonable electrical potentials. Forexample, corona wires customarily measure 0.002 inches in diameter. The wires are, therefore, also subject to neckdown failures caused by vibration. (U.S. Pat. No. 3,233,l56 to Jarvis and Robinson shows other possible corona discharge devices, however, these are unnecessarily complex.) The requirements for a corona wire, therefore, are that it'be corrosion resistant and mechanically strong. Although corona generating devices made of platinum alloys, for example, are comparatively resistant to an ozone richatmosphere, they lack the tensile strength required of corona wires.
it is, therefore, an object of this invention to provide .a system for charging an insulating or photoconductive insulating member which overcomes the above noted disadvantages.
it is another object of this invention to providea system for charging an insulating or photoconductive insulating member which does not require the corrosion resistant component to be comparatively mechanically strong.
it is another object of this invention to provide a-system for charging an insulating or photoconductive insulating member which does not require comparatively thin coronadischarge wires.
lt is another object of this invention to provide a comparatively mechanically strong, corrosion resistant corona discharge article.
It is another object of this invention to provide a corona discharge article which is comparatively useful for either positive or negative corona application.
The foregoing objects and others are accomplished in accordance with this invention by utilizing a corona discharge article comprising a core made of one or more thin wires, filamerits, or fibers, hereafter referred to as strands, overcoated with a conductive corrosion resistant material. The core provides mechanical strength and the coating provides the corrosion resistance required for corona discharge purposes. The
individual strands in the multistrand core may be placed parallel to one another but preferably are woven or twisted together to aid handling. Since the corona intensity is afunction of the surface curvature of the corona discharge device, the multistrand corona discharge core may be larger than the usual 0.002 inch corona wire because the surface curvature of the strands control the intensity of the corona generated, that is, the smaller the surface curvature of the corona discharge device is the less voltage is required to establish a usable corona. For example, a bundle of about 0.008 inches in diameter made up of about 200 individual strands, each strand measuring about 0.0004 inches in diameter may be used in place of a conventional 0.002 inch corona discharge wire. That is, the 0.008v inch bundle operating at the same potential as a 0.002 inch wire under similar conditions charges the surface of an'insulator to about the same; potential. The multistrand core corona generating article is useful for either positive or negative charging as is disclosed in U.S. Pat. No.
3,075,078 to Olden. .The preferred corona discharge device, therefore, comprises a multistrand core of quartz fibers twisted together and overcoated with a thin electrically continuous film of platinum. The quartz provides the tensile strength required of corona discharge devices and the platinum provides inertness to an:ozone'rich atmosphere and goodconductivity. ln addition,'the heterogeneous system provides increased working strength due to even distribution of stress among the'quartz fibers resulting from the use of a comparatively soft matrix.
vlt should be understood that for the-purposes of this disclosure that the term insulating-surface is intended to include'insulating and photoconductive insulating surface materials and materials such as electrographic'recording dielectrics.
Any suitable I conductive, semiconductive, or insulating material may be used as the strand material. Typical materials include strands of .quartz,'tungsten, platinum, platinumalloys, such as platinum-iridium, platinum-rhodium, etc., stainless steel, ceramics, glass, silicon carbide, boron nitride, and mixtures thereof. .Quartz is preferred because of its high'tensile strength and chemical resistivity.
The coating materialmay be of any suitable conductive material. Typical conductive metals are: aluminum, brass, cadmium, copperggold, magnesium, nickel, noble metals and their alloys such as, platinum, platinum alloys such as platinum-iridium, platinum-rhodium, palladium, iridium, rhodium, etc., silver, stainless steel, tin, tungsten, and mixtures thereof. Corrosion'resistant semiconductive materials may be used. Typical semiconductive coatings include tin oxide, indi um oxide, and siliconcarbide. Platinum is preferred because of its inertness toan ozone rich atmosphere and its relatively high conductivity.
The advantages of this improved method of imaging will become apparent uponconsideration of the detailed disclosureof the invention especially when taken in conjunction with the accompanying drawings wherein:
FlG. 1 is a cross-sectional end view of an embodiment of the corona discharge source of this invention.
FIG 2 is a cross-sectional'end view of'apreferred embodiment of the corona discharge source of this invention.
FIG 3 is anend sectional view schematically illustrating the operation of this invention.
Referring now to H6 1 a single strand cores isovercoated with conductive material 7 to form corona discharge device 8. The-coating may be applied to the core by any conventional method such as painting, spraying, dipping, plating, bychemical reaction, or by vacuum deposition. Preferably coated core 8 will not exceed in diameter conventional corona discharge devices which conventionally measure about 0.002 inches in diameter. Core Srnay be either insulating or conducting.
Referring now to FlG'Z a core comprising a plurality of fine strands 10'are overcoatedwith conductive'material lZJAlternatively, the strands 10 may be overcoated after they are twisted, woven, or placed together. Preferably strands l0 are twistedtogether to aid handling. Corona discharge device l4 may be larger than conventional corona discharge wires. The coating may be applied to the strands by any conventional method such as painting, spraying, dipping, plating, by chemical reaction, or by vacuum deposition. The allowable thickness of coating 12 depends on the number of strands in the core and on the diameter of strands 10. For example, if a very large number of small diameter strands 10 are used, a very thin coating 12 is preferred because a thick coat would fill the spaces between the outer strands 10 of the bundle resulting in loss of the small diameter surface curvature. By way of example, a core comprising 200 strands of 0.0004 inch diameter quartz should have a coating thickness in the range of 0.0000l inches to 0.00005 inches- Although P10 2 shows the overcoating to be a thin coating over the surface of the core, it is preferred to have the overcoating material penetrate to all parts of the core bundle. The
complished by moving xerographic-surface 20 at about constant speed and at approximately a right angle to the axis of discharge device 18.
The following examples further specifically illustrate the present invention. The examples below are intended to illustrate the various preferred embodiments of the improved corona generating device. The parts and percentages are by weight unless otherwise indicated. 1
EXAMPLE I A core comprising about 200 quartz fibers twisted together, each fiber measuring approximately 0.0004 inches in diameter (available from Lamp Glass Department, General Electric), is coated with Hanovia Liquid Bright Platinum 040 (available from the Hanovia Liquid Gold Division, Engelhard Industries) by brushing with a camel's hair brushdipped in the platinum solution. Sufficient solution is brushed onto the core to insure penetration of the solution into the core. The coated core is then placed in an oven and cured at a temperature of 400 C. for 1 hour. The platinum compounds decompose leaving behind a coating of pure platinum. The coated core is then recoated by brushing again with the camels hair brush dipped in the platinum solution and again baked at 400 C. for l hour to insure electrical continuity of the coating. The coating measures approximately 0.00002 inches. The coated core is then used as a corona generating article as is shown in U.S. Pat. No. 2,777,957 to Walkup.
EXAMPLE II A core comprising about 70 wound stainless steel wires each wire measuring approximately 4 microns in diameter (available from the Brunswick Corporation) is immersed in an electroplating bath comprising 13.4 ounces of ammonium nitrate, 1.3 ounces of sodium nitrate, 2.2 ounces of platinum diammino nitrate and 6.7 ounces of 28 percent ammonium hydroxide in solution in 1 gallon of water. The electroplating bath is prepared as follows: The platinum diammino nitrate is separately dissolved by heating it in a 5 percent ammonium hydroxide solution. The diammino salt is thereby changed into the tetrammino salt which is then added to the solution of ammonium nitrate, sodium nitrate and ammonium hydroxide in water. Electroplating is accomplished by applying a potential difference of about 4.5 volts until the coating measures approximately 0.00004 inches. The coated core is then used as a corona generating article.
EXAMPLE ill The experiment of example I is repeated with the exception that after the coated core is cured for the first time it is electroplated as in example ll. The resulting coating measures approximately 0.00004 inches.
EXAMPLE W A core comprising about 200 Pyrex fibers twisted together each fiber measuring approximately 0.0004 inches in diameter available from Corning Glass Works is coated with platinum as in example 1.
EXAMPLE V A core comprising about 200 Pyrex fibers twisted together each fiber measuring approximately 0.0004 inches in diameter available from Corning Glass Works is coated as in example lll.
Although specific components and proportions have been stated in the above description of preferred embodiments of the invention, other typical materials, as listed above where suitable, may be used with similar results. In addition, other materials may be added to the mixture to synergize, enhance, or otherwise modify the properties of the strands and the overcoating. For example, a material to'improve the adhesion of the overcoating to the core bundle may be incorporated within the bundle material or coated thereon.
Other modifications and ramifications of the present invention will occur to those skilled in the art upon a reading of the disclosure. These are intended to be included within the scope of this invention.
We claim:
1. The method of electrostatically charging a member which comprises placing said member in the corona discharge of a corona generating electrode comprising a core of at least two strands overcoated with an electrically continuous coating of a conductive material.
2. The method of claim 1 wherein said core comprises an insulating material.
3. The method of claim 2 wherein said core comprises quartz.
4. The method of claim 1 wherein said core comprises stainless steel.
5. The method of claim 1 wherein said overcoating comprises platinum.
Claims (5)
1. The method of electrostatically charging a member which comprises placing said member in the corona discharge of a corona generating electrode comprising a core of at least two strands overcoated with an electrically continuous coating of a conductive material.
2. The method of claim 1 wherein said core comprises an insulating material.
3. The method of claim 2 wherein said core comprises quartz.
4. The method of claim 1 wherein said core comprises stainless steel.
5. The method of claim 1 wherein said overcoating comprises platinum.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61212467A | 1967-01-27 | 1967-01-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3566108A true US3566108A (en) | 1971-02-23 |
Family
ID=24451833
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US612124A Expired - Lifetime US3566108A (en) | 1967-01-27 | 1967-01-27 | Corona generating electrode structure for use in a xerographic charging method |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3566108A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3675096A (en) * | 1971-04-02 | 1972-07-04 | Rca Corp | Non air-polluting corona discharge devices |
| US3696269A (en) * | 1970-11-12 | 1972-10-03 | Hochheiser Electronics Corp | Air processor |
| US3789278A (en) * | 1972-12-20 | 1974-01-29 | Ibm | Corona charging device |
| US3813549A (en) * | 1972-12-26 | 1974-05-28 | Ibm | Self-healing electrode for uniform negative corona |
| US3983393A (en) * | 1975-06-11 | 1976-09-28 | Xerox Corporation | Corona device with reduced ozone emission |
| US4910637A (en) * | 1978-10-23 | 1990-03-20 | Rinoud Hanna | Modifying the discharge breakdown |
| US5194291A (en) * | 1991-04-22 | 1993-03-16 | General Atomics | Corona discharge treatment |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2839400A (en) * | 1953-10-30 | 1958-06-17 | Rca Corp | Electrostatic printing |
| US3291711A (en) * | 1963-03-12 | 1966-12-13 | Du Pont | Treating electrode and process |
-
1967
- 1967-01-27 US US612124A patent/US3566108A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2839400A (en) * | 1953-10-30 | 1958-06-17 | Rca Corp | Electrostatic printing |
| US3291711A (en) * | 1963-03-12 | 1966-12-13 | Du Pont | Treating electrode and process |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3696269A (en) * | 1970-11-12 | 1972-10-03 | Hochheiser Electronics Corp | Air processor |
| US3675096A (en) * | 1971-04-02 | 1972-07-04 | Rca Corp | Non air-polluting corona discharge devices |
| US3789278A (en) * | 1972-12-20 | 1974-01-29 | Ibm | Corona charging device |
| US3813549A (en) * | 1972-12-26 | 1974-05-28 | Ibm | Self-healing electrode for uniform negative corona |
| US3983393A (en) * | 1975-06-11 | 1976-09-28 | Xerox Corporation | Corona device with reduced ozone emission |
| US4910637A (en) * | 1978-10-23 | 1990-03-20 | Rinoud Hanna | Modifying the discharge breakdown |
| US5194291A (en) * | 1991-04-22 | 1993-03-16 | General Atomics | Corona discharge treatment |
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