[go: up one dir, main page]

US2727808A - Panchromatically-sensitive zinc oxide - Google Patents

Panchromatically-sensitive zinc oxide Download PDF

Info

Publication number
US2727808A
US2727808A US387463A US38746353A US2727808A US 2727808 A US2727808 A US 2727808A US 387463 A US387463 A US 387463A US 38746353 A US38746353 A US 38746353A US 2727808 A US2727808 A US 2727808A
Authority
US
United States
Prior art keywords
zinc oxide
panchromatically
sensitive
white
tube
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
Application number
US387463A
Inventor
Soren M Thomsen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
RCA Corp
Original Assignee
RCA Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by RCA Corp filed Critical RCA Corp
Priority to US387463A priority Critical patent/US2727808A/en
Priority to US513398A priority patent/US2727807A/en
Application granted granted Critical
Publication of US2727808A publication Critical patent/US2727808A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/08Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being inorganic
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G9/00Compounds of zinc
    • C01G9/02Oxides; Hydroxides

Definitions

  • Electrostatic printing is, generally, that type of process for producing a visible image, reproduction or copies which includes as an intermediate step converting a light image or signal into an electrostatic charge pattern on an insulating. surface.
  • a light image is focused upon the charged surface whereby the elemental areas irradiated by the light rays are discharged, leaving a charge on the remainder of the surface forming an electrostatic image.
  • the electrostatic image is rendered visible by the application of a developer powder which is held electrostatically to the charged areas of the sheet.
  • Thepowder image thus formed may be fixed directly to the coated surface of the sheet.
  • White zinc oxide is known to have desirable photoconducting properties.
  • a coating of white zinc oxide in an insulating film-forming vehicle also is known for its ability to hold a blanket electrostatic charge or an electrostatic image for considerable periods of time.
  • electrostatic images may be formed on a sheet of a base material coated or impregnated with this type of composition.
  • the spectral sensitivity of the white zinc oxide coating is limited to the ultraviolet and the blue end of the visible spectrum. Hence its use is limited to those processes where there is a radiation source within these spectral limits.
  • Pure zinc oxide also occurs in a second form which has been variously described as red, buff, salmon or brown in color.
  • This material has a greater spectral sensitivity in the visible region of the spectrum than white zinc oxide.
  • this second form of zinc oxide may be prepared by heating the hydrolytic products of an ammoniacal zinc nitrate solution, or by deagrating white zinc oxide with ammonium nitrate or by fusing white zinc oxide with certain ammonium salts. These methods have the disadvantage that at least one wet process step is necessary. Ammoniacal zinc nitrate is prepared by a wet process. The other methods have a relatively low yield of the colored form of zinc oxide, which must be separated by elutriation. Furthermore, the colored oxide produced by previously known methods has a relatively low photosensitivity.
  • Another object is to provide a method of preparing Zinc oxide that is photosensitive over the entire range of the visible spectrum.
  • a further object is to provide a method of preparing a zinc oxide that may be used to produce a panchromati-V cally-sensitive coating on paper.
  • Another object is to provide an improved dry process method of preparing panchromatically-sensitive zinc oxide.
  • one embodiment of the present invention which comprises reacting white zinc oxide with carbon dioxide gas and ammonia gas and then heating the reaction product at a temperature between 150 land 400 C.
  • a second embodiment comprises heating an intimate mixture of white zinc oxide and ammonium carbamate acid carbonate at a temperature between 15 0 and 400 C.
  • Figure 1 is a sectional view of an apparatus which may be used to carry out the process of this invention.
  • Figure 2 is a graph showing the distribution of spectral sensitivity in Angstrom units ⁇ of ordinary white zinc oxide and a panchromatically-sensitive zinc oxide.
  • Example l Referring to Figure 1, a Pyrex tube 21 about l in diameter and 12" long is filled with about 50 grams of chemically pure dry process zinc oxide 23. Glass wool plugs 25 are fitted at both ends of the zinc oxide to hold the zinc oxide in place. A rubber stopper 27 is litted into one end of the tube 21. A carbon dioxide inlet tube 29 and an ammonia inlet tube 31 extend through the rubber stopper 27 into the glass wool plug 25.
  • Example 2 Another mediod for preparing the zinc oxide of the instant invention is to mix two parts by weight of ammonium carbamate acid carbonate with about one part of chemically pure dry process zinc oxide. The mixture is then placed in an oven and baked in the same manner as described in Example 1.
  • the products of the above methods are brown in color. Although the product is slightly caked, it is friable and therefore easily removed and powdered. If less than 50 grams of carbon dioxide and ammonia gas mixture is absorbed in Example 1, or less than 2 parts of ammonium carbamate acid carbonate is added in Example 2, lighter colored products result.
  • the zinc oxide of this invention may be prepared by heating the mixtures in Example 1 or 2, between about 150 and 400 C. for an hour or more. However, the higher the temperature and the longer the heating, the darker in color the resultant product will be. 1f the material is heated at a temperature above 400 C., it is converted from the panchrornaticallysensitive variety to the ordinary white Variety of zinc oxide.
  • the products of the above two methods have an odor of ammonia which may be removed by further baking at about 250 C. in an oven having air circulation. Such removal may be either desirable or unnecessary depending upon the use for which the zinc oxide is intended.
  • ordinary White zinc oxide such as the type used at the start of the instant process, is' a photoconductor at ordinary temperatures with a spectral sensitivity in the ultraviolet aud the blue end of the visible spectrum as indicated by curve 41.
  • the material produced by the instant process is also a photoconductor but exhibits a spectral sensitivity over the entire visible spectrum as indicated by curve 43.
  • the spectral sensitivity of the zinc oxide is shifted to the longer wavelengths by the instant process.
  • the curves 41 and 43 of Figure 2 are not to the same ordinate scale.
  • the zinc oxide of the instant invention may be mixed with an insulating film-forming resin, such as polyvinyl chloride, and coated on paper to produce a photosensitive sheet.
  • the coating is photoconductive over the entire range of the visible spectrum.
  • the zinc oxide of the instant invention may also be pressed into pellets and used as the active element of a photoconductive cell.
  • a dry process for making panchromatically-sensitive zinc oxide which comprises reacting white zinc oxide with carbon dioxide gas' and ammonia gas and then heating the reaction product at a temperature between about 150 and 400 C.
  • a dry process for making panchromatically-sensitive zinc oxide which comprises reacting white zinc oxide with carbon dioxide gas and ammonia gas until there is a weight increase in the zinc oxide of about baking the reaction product at about C. for about one hour and then heating the baked reaction product at about 250 C. for about one hour.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Paper (AREA)

Description

Dec. 20, 1955 s. M. THoMsEN PANCHROMATICALLY-SENSITIVE ZINC OXID Filed Oct. 21, 1953 im zu 41'@ ma im m I N VEN TOR. brenNh//Lferb ATTORNEY United States PatentO PANcHRoMAncALLY-SENSITIVE ZINC oxIDE Soren M. Thomsen, Pennington, N. J., assignor to Radio Corporation of America, a corporation of Delaware Application October 21, 1953, Serial No. 387,463 2 Claims. (Cl. 23--147) This invention relates to zinc oxide and more particularly to an improved method of preparing zinc oxide that is photosensitive over the entire range of the Visible spectrum. y
The zinc oxide made by the improved method of the present invention has been found to be particularlyuseful in electrostatic printing processes. Electrostatic printing is, generally, that type of process for producing a visible image, reproduction or copies which includes as an intermediate step converting a light image or signal into an electrostatic charge pattern on an insulating. surface. H. G. Greig in U. S. patent application Serial No. 248,937, filed September 29, 1951, now abandoned but which is now embodied in U. S. continuation-in-part patent application Serial No. 383,677, filed October 1, 1953, describes a process wherein a sheet of paper or other conducting material is coated with a photoconductor such as zinc oxide in an insulating film-forming vehicle, then a blanket electrostatic charge is applied to the coated surface of the sheet. A light image is focused upon the charged surface whereby the elemental areas irradiated by the light rays are discharged, leaving a charge on the remainder of the surface forming an electrostatic image. The electrostatic image is rendered visible by the application of a developer powder which is held electrostatically to the charged areas of the sheet. Thepowder image thus formed may be fixed directly to the coated surface of the sheet.
White zinc oxide is known to have desirable photoconducting properties. A coating of white zinc oxide in an insulating film-forming vehicle also is known for its ability to hold a blanket electrostatic charge or an electrostatic image for considerable periods of time. Thus, electrostatic images may be formed on a sheet of a base material coated or impregnated with this type of composition. However, the spectral sensitivity of the white zinc oxide coating is limited to the ultraviolet and the blue end of the visible spectrum. Hence its use is limited to those processes where there is a radiation source within these spectral limits.
Pure zinc oxide also occurs in a second form which has been variously described as red, buff, salmon or brown in color. This material has a greater spectral sensitivity in the visible region of the spectrum than white zinc oxide. It is known that this second form of zinc oxide may be prepared by heating the hydrolytic products of an ammoniacal zinc nitrate solution, or by deagrating white zinc oxide with ammonium nitrate or by fusing white zinc oxide with certain ammonium salts. These methods have the disadvantage that at least one wet process step is necessary. Ammoniacal zinc nitrate is prepared by a wet process. The other methods have a relatively low yield of the colored form of zinc oxide, which must be separated by elutriation. Furthermore, the colored oxide produced by previously known methods has a relatively low photosensitivity.
It is an object of this invention to provide a method ICC of preparing zinc oxide having improved photoconductive properties.
Another object is to provide a method of preparing Zinc oxide that is photosensitive over the entire range of the visible spectrum.
A further object is to provide a method of preparing a zinc oxide that may be used to produce a panchromati-V cally-sensitive coating on paper.
Another object is to provide an improved dry process method of preparing panchromatically-sensitive zinc oxide.
The foregoing objects and other advantages may be accomplished by one embodiment of the present invention which comprises reacting white zinc oxide with carbon dioxide gas and ammonia gas and then heating the reaction product at a temperature between 150 land 400 C.
A second embodiment comprises heating an intimate mixture of white zinc oxide and ammonium carbamate acid carbonate at a temperature between 15 0 and 400 C.
The invention will be described in greater detail by reference to the accompanying drawing in which:
Figure 1 is a sectional view of an apparatus which may be used to carry out the process of this invention, and
Figure 2 is a graph showing the distribution of spectral sensitivity in Angstrom units `of ordinary white zinc oxide and a panchromatically-sensitive zinc oxide.
Example l Referring to Figure 1, a Pyrex tube 21 about l in diameter and 12" long is filled with about 50 grams of chemically pure dry process zinc oxide 23. Glass wool plugs 25 are fitted at both ends of the zinc oxide to hold the zinc oxide in place. A rubber stopper 27 is litted into one end of the tube 21. A carbon dioxide inlet tube 29 and an ammonia inlet tube 31 extend through the rubber stopper 27 into the glass wool plug 25.
About one hundred milliliters per minute of carbon dioxide and ammonia are passed through inlet tubes 29 and 31 into the zinc oxide 23 in the tube 21. The gases react with the zinc oxide raising the temperature within the tube as high as C. After about 30 minutes, the gas flow may be stopped and the stopper 27 with the inlet tubes 29 and 31 removed and placed in the opposite end of the tube. The gas flow is again continued for about one hour. The purpose of moving the stopper and inlet tubes to the opposite end of the tube is only to facilitate even distribution of gases through the zinc oxide 23. The tube contents increase in weight by about 50 grams during this period. The rubber stopper 27 and the inlet tubes 29 and 31 are removed and the tube 21 with its contents is placed in an oven and baked at about C. for about an hour, and then the temperature is raised to 250 C. for another hour. The color of the material in the tube 21 changes in color from white to brown during the last hour of baking. The tube and contents are then removed from the oven and allowed to cool.
Example 2 Another mediod for preparing the zinc oxide of the instant invention is to mix two parts by weight of ammonium carbamate acid carbonate with about one part of chemically pure dry process zinc oxide. The mixture is then placed in an oven and baked in the same manner as described in Example 1.
The products of the above methods are brown in color. Although the product is slightly caked, it is friable and therefore easily removed and powdered. If less than 50 grams of carbon dioxide and ammonia gas mixture is absorbed in Example 1, or less than 2 parts of ammonium carbamate acid carbonate is added in Example 2, lighter colored products result. The zinc oxide of this invention may be prepared by heating the mixtures in Example 1 or 2, between about 150 and 400 C. for an hour or more. However, the higher the temperature and the longer the heating, the darker in color the resultant product will be. 1f the material is heated at a temperature above 400 C., it is converted from the panchrornaticallysensitive variety to the ordinary white Variety of zinc oxide. The products of the above two methods have an odor of ammonia which may be removed by further baking at about 250 C. in an oven having air circulation. Such removal may be either desirable or unnecessary depending upon the use for which the zinc oxide is intended.
Referring to Figure 2, ordinary White zinc oxide, such as the type used at the start of the instant process, is' a photoconductor at ordinary temperatures with a spectral sensitivity in the ultraviolet aud the blue end of the visible spectrum as indicated by curve 41. The material produced by the instant process is also a photoconductor but exhibits a spectral sensitivity over the entire visible spectrum as indicated by curve 43. In general, the spectral sensitivity of the zinc oxide is shifted to the longer wavelengths by the instant process. The curves 41 and 43 of Figure 2 are not to the same ordinate scale.
The zinc oxide of the instant invention may be mixed with an insulating film-forming resin, such as polyvinyl chloride, and coated on paper to produce a photosensitive sheet. The coating is photoconductive over the entire range of the visible spectrum. The zinc oxide of the instant invention may also be pressed into pellets and used as the active element of a photoconductive cell.
There has thus been described a dry process method for making a panchromatically-sensitive zinc oxide which is cheap, economical and simple to produce.
What is claimed is:
1. A dry process for making panchromatically-sensitive zinc oxide which comprises reacting white zinc oxide with carbon dioxide gas' and ammonia gas and then heating the reaction product at a temperature between about 150 and 400 C.
2. A dry process for making panchromatically-sensitive zinc oxide which comprises reacting white zinc oxide with carbon dioxide gas and ammonia gas until there is a weight increase in the zinc oxide of about baking the reaction product at about C. for about one hour and then heating the baked reaction product at about 250 C. for about one hour.
References Cited in the le of this patent UNITED STATES PATENTS 2,585,461 Hirsch Feb. 12, 1952 FOREIGN PATENTS 558,213 Great Britain Dec. 24, 1943 OTHER REFERENCES J. W. Mellors A Comprehensive Treatise on Inorganic and Theoretical Chem., Vol. VI, page 69. Longmans, Green and Co., New York.

Claims (1)

1. A DRY PROCESS FOR MAKING PANCHROMATICALLY-SENSITIVE ZINC OXIDE WHICH COMPRISES REACTING WHITE ZINC OXIDE WITH CARBON DIOXIDE GAS AND AMMONIA GAS AND THEN HEATING THE REACTION PRODUCT AT A TEMPERATURE BETWEEN ABOUT 150* AND 400* C.
US387463A 1953-10-21 1953-10-21 Panchromatically-sensitive zinc oxide Expired - Lifetime US2727808A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US387463A US2727808A (en) 1953-10-21 1953-10-21 Panchromatically-sensitive zinc oxide
US513398A US2727807A (en) 1953-10-21 1955-06-06 Panchromatically-sensitive zinc oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US387463A US2727808A (en) 1953-10-21 1953-10-21 Panchromatically-sensitive zinc oxide

Publications (1)

Publication Number Publication Date
US2727808A true US2727808A (en) 1955-12-20

Family

ID=23529977

Family Applications (1)

Application Number Title Priority Date Filing Date
US387463A Expired - Lifetime US2727808A (en) 1953-10-21 1953-10-21 Panchromatically-sensitive zinc oxide

Country Status (1)

Country Link
US (1) US2727808A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2917385A (en) * 1955-08-26 1959-12-15 Haloid Xerox Inc Reflex xerography
US2963365A (en) * 1956-02-16 1960-12-06 Rca Corp Electrostatic printing
US3003870A (en) * 1957-04-17 1961-10-10 Eastman Kodak Co Alteration of characteristic curve of zinc oxide electrophotographic materials
US3052540A (en) * 1954-06-02 1962-09-04 Rca Corp Dye sensitization of electrophotographic materials
US3060134A (en) * 1959-03-03 1962-10-23 New Jersey Zinc Co Photoconductive zinc oxide pigment
US3060019A (en) * 1958-07-22 1962-10-23 Rca Corp Color electrophotography
US3250613A (en) * 1961-05-01 1966-05-10 Eastman Kodak Co Use of amines in photoconductographic coatings
US3429662A (en) * 1965-03-15 1969-02-25 American Zinc Co Zinc oxide
DE2519064A1 (en) * 1974-05-03 1975-11-20 Oce Van Der Grinten Nv PANCHROMATIC SENSITIVE ZINC OXIDE AND THE PROCESS FOR THE PRODUCTION AND USE THEREOF
US4071609A (en) * 1975-07-09 1978-01-31 The New Jersey Zinc Company Method for preparing particulate zinc oxide shapes of high surface area and improved strength
JPS5363023A (en) * 1976-11-18 1978-06-06 Fujitsu Ltd Zinc oxide manufacture

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB558213A (en) * 1941-07-18 1943-12-24 British Thomson Houston Co Ltd Improvements in and relating to fluorescent materials
US2585461A (en) * 1946-01-04 1952-02-12 Benjamin L Hirsch Method of making fluorescent zinc oxide

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB558213A (en) * 1941-07-18 1943-12-24 British Thomson Houston Co Ltd Improvements in and relating to fluorescent materials
US2585461A (en) * 1946-01-04 1952-02-12 Benjamin L Hirsch Method of making fluorescent zinc oxide

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3052540A (en) * 1954-06-02 1962-09-04 Rca Corp Dye sensitization of electrophotographic materials
US2917385A (en) * 1955-08-26 1959-12-15 Haloid Xerox Inc Reflex xerography
US2963365A (en) * 1956-02-16 1960-12-06 Rca Corp Electrostatic printing
US3003870A (en) * 1957-04-17 1961-10-10 Eastman Kodak Co Alteration of characteristic curve of zinc oxide electrophotographic materials
US3060019A (en) * 1958-07-22 1962-10-23 Rca Corp Color electrophotography
US3060134A (en) * 1959-03-03 1962-10-23 New Jersey Zinc Co Photoconductive zinc oxide pigment
US3250613A (en) * 1961-05-01 1966-05-10 Eastman Kodak Co Use of amines in photoconductographic coatings
US3429662A (en) * 1965-03-15 1969-02-25 American Zinc Co Zinc oxide
DE2519064A1 (en) * 1974-05-03 1975-11-20 Oce Van Der Grinten Nv PANCHROMATIC SENSITIVE ZINC OXIDE AND THE PROCESS FOR THE PRODUCTION AND USE THEREOF
JPS50153938A (en) * 1974-05-03 1975-12-11
US4013783A (en) * 1974-05-03 1977-03-22 Oce-Van Der Grinten N.V. Panchromatically sensitive zinc oxide
JPS5613942B2 (en) * 1974-05-03 1981-04-01
US4071609A (en) * 1975-07-09 1978-01-31 The New Jersey Zinc Company Method for preparing particulate zinc oxide shapes of high surface area and improved strength
JPS5363023A (en) * 1976-11-18 1978-06-06 Fujitsu Ltd Zinc oxide manufacture
JPS5615500B2 (en) * 1976-11-18 1981-04-10

Similar Documents

Publication Publication Date Title
US2727808A (en) Panchromatically-sensitive zinc oxide
US2735785A (en) Process of electrostatic printing
US2907674A (en) Process for developing electrostatic image with liquid developer
GB940577A (en) A process for the production of electrophotographic images
US2735784A (en) Process of electrostatic printing
US2844733A (en) Reflex thermoprinting
JPS55166647A (en) Photoconductive composition and electrophotographic receptor using this
GB956772A (en) Xerographic process
US2727807A (en) Panchromatically-sensitive zinc oxide
US3060134A (en) Photoconductive zinc oxide pigment
JPS5652757A (en) Electrophotographic copying material
GB1102340A (en) A method of thermographic reproduction
US3674476A (en) Process for producing photoconductive layer for electrophotography
US3453141A (en) Method for making a high-speed reusable x-ray plate using orthorhombic lead oxide and resulting article
GB798097A (en) Xerographic development
GB963645A (en) Improved process for producing images in electric-photography and electro-radiography
US3494789A (en) Photoconductive insulating material
US4366222A (en) Cadmium sulfide/cadmium carbonate/cadmium oxide photoconductor produced by high temperature, inert atmosphere calcination
JPS548529A (en) Production of sintered type electrophotographic photoreceptor
US3565713A (en) Method of forming a ceramic image on a ceramic substrate
US3627528A (en) Electrophotographic recording element having photoconductor with quenched luminescence during charging and method of making the photoconductor
US2862817A (en) Crystalline selenium plate
US3589928A (en) Process for the production of a light sensitive material for electrophotography
US4013783A (en) Panchromatically sensitive zinc oxide
US3506595A (en) Photoconductive insulating material