US3428452A - Photoconductive compositions and electrophotographic recording elements made therefrom - Google Patents
Photoconductive compositions and electrophotographic recording elements made therefrom Download PDFInfo
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- US3428452A US3428452A US426443A US3428452DA US3428452A US 3428452 A US3428452 A US 3428452A US 426443 A US426443 A US 426443A US 3428452D A US3428452D A US 3428452DA US 3428452 A US3428452 A US 3428452A
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- 239000000203 mixture Substances 0.000 title description 30
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 142
- 239000000243 solution Substances 0.000 description 84
- 239000011248 coating agent Substances 0.000 description 77
- 238000000576 coating method Methods 0.000 description 76
- 239000011787 zinc oxide Substances 0.000 description 71
- 229920005989 resin Polymers 0.000 description 65
- 239000011347 resin Substances 0.000 description 65
- 239000002245 particle Substances 0.000 description 58
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 49
- 239000000758 substrate Substances 0.000 description 41
- 239000000975 dye Substances 0.000 description 39
- 238000000034 method Methods 0.000 description 39
- 239000011230 binding agent Substances 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000008240 homogeneous mixture Substances 0.000 description 16
- 239000004615 ingredient Substances 0.000 description 13
- 238000001035 drying Methods 0.000 description 12
- 239000008393 encapsulating agent Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 8
- 229920013620 Pliolite Polymers 0.000 description 7
- 238000001694 spray drying Methods 0.000 description 7
- 238000003795 desorption Methods 0.000 description 6
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- 238000002156 mixing Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- -1 however Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 229920003002 synthetic resin Polymers 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 238000013019 agitation Methods 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
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- 239000000126 substance Substances 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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- 206010070834 Sensitisation Diseases 0.000 description 3
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- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
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- 239000000025 natural resin Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
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- 229920000728 polyester Polymers 0.000 description 2
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- 238000003756 stirring Methods 0.000 description 2
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- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000001429 visible spectrum Methods 0.000 description 2
- KWVPFECTOKLOBL-KTKRTIGZSA-N 2-[(z)-octadec-9-enoxy]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCO KWVPFECTOKLOBL-KTKRTIGZSA-N 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- 206010010071 Coma Diseases 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- DPKHZNPWBDQZCN-UHFFFAOYSA-N acridine orange free base Chemical compound C1=CC(N(C)C)=CC2=NC3=CC(N(C)C)=CC=C3C=C21 DPKHZNPWBDQZCN-UHFFFAOYSA-N 0.000 description 1
- 229940074323 antara Drugs 0.000 description 1
- JPIYZTWMUGTEHX-UHFFFAOYSA-N auramine O free base Chemical compound C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 JPIYZTWMUGTEHX-UHFFFAOYSA-N 0.000 description 1
- DZBUGLKDJFMEHC-UHFFFAOYSA-N benzoquinolinylidene Natural products C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- NJDNXYGOVLYJHP-UHFFFAOYSA-L disodium;2-(3-oxido-6-oxoxanthen-9-yl)benzoate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=CC(=O)C=C2OC2=CC([O-])=CC=C21 NJDNXYGOVLYJHP-UHFFFAOYSA-L 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- YMTINGFKWWXKFG-UHFFFAOYSA-N fenofibrate Chemical compound C1=CC(OC(C)(C)C(=O)OC(C)C)=CC=C1C(=O)C1=CC=C(Cl)C=C1 YMTINGFKWWXKFG-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- 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
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0525—Coating methods
Definitions
- This invention relates generally to photoconductive compositions which are particularly useful in electrophotography. Particularly, the invention relates to improved photoconductive layers, containing dye-sensitized photoconductors, and improved methods of making these layers from aqueous coating solutions.
- aqueous coating solution as used herein, is meant a dispersion of a dye-sensitized photoconductor in water in which a resinous binding agent is either dissolved or dispersed.
- a resinous binding agent is either dissolved or dispersed.
- a white body colored photoconductor such as zinc oxide
- a coating solution that comprises a lightsensitizing dye, zinc oxide, and a resin binder for the zinc oxide in a liquid vehicle other than water.
- Organic solvents such as toluene and methyl ethyl ketone, for example, in which light-sensitizing dyes are substantially insoluble, have been used heretofore as the liquid vehicle for photoconductive coating solutions to prevent desorption of the dye into the liquid.
- organic solvent coating solutions are relatively expensive, dangerous to handle, and usually present a fire hazard in a factory or paper mill.
- the dyes desorbed by the water would tend to objectionably color the substrate of an electrophotographic recording element to which the photoconductive coating was applied, leaving uneven colored streaks. Because of this objectionable desorption of the dyes in water, an excessive quantity of dyes had to be used, resulting in an excessive waste of the dyes and uneven sensitization. Also, it has often been impossible to obtain the same degree of light sensitization of the photoconductive layers from prior art aqueous coating solutions as has been obtained from non-aqueous coating solutions because of the objectionable desorption of the dyes in water.
- Another object of the present invention is to provide improved methods of producing photoconductive compositions employing an aqueous solution of dye-sensitized photoconductive particles whose dyes are not easily desorbed in aqueous coating solutions.
- Still another object of the present invention is to provrde improved photoconductive layers and improved methods of making them that overcome the aforementioned disadvantages of employing light-sensitizing dyes in prior art aqueous coating solutions.
- Still a further object of the present invention is to provide improved photoconductive layers that may be applied, by the improved methods of the present invention, directly, safely, and economically to a web of substrate record material, such as paper, during its manufacture.
- the improved photoconductive layers of the present invention are applied to suitable subtrates from aqueous coating solutions containing particles of completely encapsulated dye-sensitized zinc oxide dispersed in an aqueous film-forming emulsion of a natural and/or synthetic resin.
- the aqueous resin emulsion functions as a film-forming vehicle and, after drying, functions as a resinous binding agent for the encapsulated dye-sensitized particles.
- Each of the encapsulated dye-sensitized particles comprises a core of a photoconductive material such as zinc oxide, at least one light-sensitizing dye adsorbed to the photoconductor, and a substantially waterproof resin encapsulating the dye photoconductor.
- the particles of encapsulated dye-sensitized photoconductor can be produced, in a preferred method of the present invention, by first making a homogeneous mixture of photoconductive zinc oxide, a solution of at least one light-sensitizing dye, and a solution of a resin in a suitable solvent for the resin and then spray-drying the homogeneous mixture under conditions to form encapsulated particles of a desired average diameter.
- Encapsulated dye-sensitized zinc oxide particles of the type described herein will be hereinafter referred to as EDSZO.
- the quantitative ratios between the zinc oxide, the dyes and the encapsulant therefor may vary within wide limits depending upon the degree of light sensitization desired and/or the coating solutions in which the EDSZO is to be included.
- the weight ratio of dyed zinc oxide to resin encapsulant may be as small as 2:1 and as great as 7.5 :1.
- the weight ratio of dyed zinc oxide to the total resin in the aqueous coating solution may be as little as 2:1 and as great as 3:1.
- particles of EDSZO can be fused directly onto a backing substrate, without being deposited from a solution, to form a suitable photoconductive layer.
- One method of preparing EDSZO in accordance with the present invention is:
- EXAMPLE 1 A concentrated stock solution of a light-sensitizing dye mixture is prepared by making a solution of 0.5 g. of Brilliant Blue FCF (42090 Color Index Acid Blue 9- 2nd ed. 1957) and 0.01 g. of fluorescein in 197.5 of ethanol.
- Brilliant Blue FCF 42090 Color Index Acid Blue 9- 2nd ed. 1957
- a one percent by weight solution of Pliolite SD resin in toluene is prepared.
- the dried dyed zinc oxide is mixed with the one percent 'Pliolite S-SD resin solution in toluene in the proportions of 5 g. of the dried died zinc oxide for each 45 ml. of the Pliolite 'S-SD solution in a ball mill for 2 hours.
- the milled mixture is spread thinly on glass and the toluene is evaporated leaving dried, died zinc oxide encapsulated in the Pliolite S5D resin.
- the dried, encapsulated dyed zinc oxide is scraped off the glass surface and then ground in a mortar to a fine powder of particles averaging about 1 micron in diameter.
- the quantities of ingredients of Example 1 may vary so that the Weight ratio of the zinc oxide to the encapsulating resin may be within the range of 27.5: l.
- the photoconductive zinc oxide used in this and the following examples may, for example, be either Florence Green Seal No. 8 or Photox 801, products of the New Jersey Zinc Company, Palmerton, Pa.
- Pliolite S-SD is a synthetic resin of the high styrene butadiene copolymer type, a product of the Goodyear Tire and Rubber Company.
- EDSZO made pursuant to Example 1 is photoconductive in response to wavelengths of light over the entire visible spectrum.
- the encapsulating resin of the dye-sensitized zinc oxide may by the (laboratory) method of Example 1 should be hard and grindable to produce a fine powder.
- Soft, as well as hard, resinous waterproofing encapsulants for the dye-sensitized zinc oxide may be used to prepare EDSZO by the following preferred (commercial) method of Example 2, employing the technique of spray drying:
- EXAMPLE 2 A light-sensitizing dye, Blue Concentrate, is prepared by dissolving 1.2 g. of fiuorescein disodium salt and 3.6 g. of Brilliant Blue FCF in 100 ml. of methanol.
- a homogeneous mixture is made of 454 g. of photoconductive zinc oxide, 2 ml. of the aforementioned Blue Concentrate, 60 g. to 240 g. (preferably 120 g.) of Pliolite S-5E (a high styrene butadiene copolymer resin) and 800 ml. of toluene.
- the homogeneous mixture is then spray dried in a Bowen Conical Laboratory Spray Drier (Bowen Engineering, Inc., North Branch, NJ.) under the following conditions: Feed (rate 98 cc./min., air-inlet temperature to drying chamber 208 F., air-outlet temperature of drying chamber 155 F.
- Example 2 Indirect gas heat is used, and a concurrent flow in a two-fluid nozzle atomizer is obtained with an air pressure input to the nozzle of about 100 lb./in. gage.
- the aforementioned quantities in Example 2 may vary so that the ratio of zinc oxide to the resin encapsulant may vary from 2 to 75:1 by weight.
- the EDSZO formed by the preferred method of Example 2 comprises substantially spherical particles of about 1 micron in diameter.
- Each of the particles of EDSZO comprises a core of photoconductive dyesensitized zinc oxide completely encapsulated by the waterproof resin (Pliolite S5E).
- the spray drying method (Example 2) of producing EDSZO" is preferred to the grinding method of Example 1 because it can be adapted to a closed cycle wherein the solvent of the encapsulating resin may be recovered, if desired.
- the spray drying method permits the use of a wide choice of both hard and soft encapsulating natural or synthetic resins because the operation of grinding to form a fine powder is obviated.
- the spray drying method is a practical commercial method, resulting in uniform, substantially spherical, completely encapsulated dye-sensitized, photoconductive zinc oxide particles.
- the EDSZO Being encapsulated in a waterprof resin, the EDSZO can now be incorporated in photoconductive coating solulions (dispersions) that have a water base.
- the encapsulant on each particle of EDSZO prevents desorption of the light-sensitizing dyes into the aqueous photoconductive coating solutions.
- An aqueous coating (film forming) solution for forming a photoconductive layer on a suitable substrate, such as paper, may be prepared as follows:
- EXAMPLE 3 PART A Parts by Ingredients Weight Supplier (grams) EDSZO (prepared in accordance 15.0 (As per Example 2).
- PART C Piccotex No. 131-119 (a water emul- 9. 0 Penn. Industrial sion of a styrene homolog copoly- Chemical Corp., met, a resin). Clareton, Pa. Water 15.0 FMC KP- (tributoxy ethyl phos- 0. 5 Food Machinery phate, a plasticizer and leveling Mix together the ingredients of Part B. Add Part A to Part B and mix in a ball mill for about one hour. Mix Part C ingredients together and add to the combined Parts A and B and mix by stirring to form the aqueous coating solution.
- the coating solution to a suitable substrate, such as paper or a metal sheet, of an electrophotographic recording element, as by flow-coating, and dry the coated substrate at about C. for about 2 minutes.
- the encapsulant (Pliolite S-SE) of the EDSZO and the resin (Piccotex 131-119) of the aqueous photoconductive coating solution tend to fuse together to form the photoconductive layer of the electrophotographic recording element.
- the quantities of the ingredients of Example 3 may be varied so that the ratio of zinc oxide to the total quantity of resin (Pliolite S-SE and Piccotex 131419) in the aqueous coating solution is within the range of 23:1 by weight.
- the photoconductive layer so formed is superior in its sensitivity to visible light to photoconductive layers of the prior art formed from aqueous coating solutions.
- the electrophotographic recording element so produced may be processed in the usual manner for producing electrophotographic images.
- the electrophotographic recording element is first made sensitive to light by applying an electrostatic charge to the photoconductive layer in the dark.
- the electrostatic charge may be applied by any means known in the art, such as by a corona discharge device.
- the photoconductive layer is then exposed to a light image to discharge it selectively and to provide a conductivity pattern, that is, a latent image, thereon.
- the latent image may be developed by applying a pigmented resin powder of suitable electrostatic charge to the exposed photoconductive layer.
- Another aqueous coating solution employing EDSZO, for coating the conductive substrate of an electrophotographic recording element with an improved U-3101 UBATOL (14% solids by weight, water suspensions and acrylato polymer resin).
- polyester a resin of 14% solids in an alkali-soluble solution.
- Part B is prepared as follows: Add 1 part 26 B. of ammonia to 43.6 parts by weight of cold water. Stir in 7.4 parts by weight of alkali-soluble resin (Durez 15546) using moderate but thorough agitation. Heat and add 1 part by weight of ammonia (26 B.) until solution is complete. Keep the solution cool until used.
- KP-MO tnbutoxy ethyl phos- 0.7 Food Machinery Corp.
- Example 4 Add in the proportions of 7 g. of EDSZO, 5 ml. of water, and 5 ml. of the homogeneous mixture of Parts A, B, C, and D and mix until the EDSZO particles are evenly dispersed in the mixture, thus forming the desired aqueous photoconductive coating solution.
- This coating solution may be used to flow-coat any suitable conductive substrate to apply the improved photoconductive layer thereto.
- the quantities of the ingredients of Example 4 may be varied, as desired, to provide an aqueous coating solution in which the ratio of zinc oxide to the total quantity of resin in the solution is 23:1 by Weight, (Zinc oxideztotal resin).
- EXAMPLE 5 Component- Percent by weight Carnauba Wax 22 Stearic acid 2 Diethanolamine 1 Water 75
- the diethanolamine is dissolved in the water and heated to 200-210 F.
- the stearic acid is dissolved in the wax at ZOO-210 F.
- the hot Wax solution is poured slowly into the hot water solution While maintaining vigorous agitation. The agitation is continued until the solution becomes smooth and homogeneous.
- Proportionately, 5 g. of EDSZO, prepared in accordance with Example 2 is dispersed in 10 ml. of the aforementioned homogeneous solution (emulsion) to form the aqueous photoconductive coating solution.
- This quantities of the ingredients in Example 5 may be varied so that the ratio of zinc oxide to the total quantity of resin (carnauba wax and Pliolite S-SE) in the coating solution is from 2-3z1 by weight, (zinc oxideztotal resin in coating solution).
- This coating solution can be applied to any suitable substrate, as by flow-coating, as described for the aqueous photoconductive coating solution of Example 3.
- Each of the aqueous coating solutions described in Examples 3, 4, and 5 is essentially a dispersion of EDSZO in an aqueous solution (mixture, dispersion, or emulsion) of a resinous binding agent for the EDSZO.
- the aqueous coating solutions described in Examples 3, 4, and 5 differ from each other primarily in the type of resinous binding agent (natural and/or synthetic) used and in the type of wetting agents, leveling agents, and surfactants employed.
- the EDSZO may be dispersed in a large number of aqueous mixtures of resinous binding agents to provide an improved aqueous coating solution wherein desorption of the light-sensitizing dye into the Water vehicle of the coating solution is substantially prevented.
- An aqueous coating solution for forming a photoconductive layer on a substrate comprising particles of a resin-encapsulated dye-sensitized photoconductive zinc oxide dispersed in an aqueous mixture comprising a resinous binding agent, the sensitizing dye of said particles being water soluble, and the encapsulating resin of said particles being water insoluble.
- An aqueous coating solution for forming a photoconductive layer on a substrate comprising particles of a resin-encapsulated dye-sensitized zinc oxide dispersed in an aqueous mixture comprising a resinous binding agent, the ratio of zinc oxide to the total quantity of the resin of said encapsulant and said binding agent in said coating solution being within a range of about 2 to 3:1 by weight, the sensitizing dye of said particles being water soluble, and the encapsulating resin of said particles being water insoluble.
- An aqueous coating solution for forming a photoconductive layer on a substrate of an electrophotographic recording element comprising particles of encapsulated dye-sensitized zinc oxide dispersed in an aqueous mixture comprising a resinous binding agent, each of said particles comprising a core of photoconductive zinc oxide,
- An aqueous coating solution for forming a photoconductive layer of an electrophotographic recording element comprising particles of encapsulated dye-sensitized zinc oxide dispersed in an aqueous mixture comprising a resin, each of said particles comprising a core of photoconductive zinc oxide,
- each of said particles having a diameter of about 1 micron.
- the method of storming a photoconductive layer on a substrate of an electrophotographic recording element comprising the steps of mixing together zinc oxide particles, a water soluble light-sensitizing dye, a resin substantially insoluble in water, and a solvent for said resin, whereby to dye-sensitize said zinc oxide particles and coat the sensitized particles with resin,
- a method of forming a photoconductive layer on a substrate of an electrophotographic recording element said layer comprising particles of resin-encapsulated dyesensitized zinc oxide wherein each particle comprises a core of zinc oxide, a water soluble dye adsorbed to said core, and a water soluble resin encapsulating said dyed core, said method comprising dispersing said particles of resin-encapsulated dyesensitized zinc oxide particles homogeneously in an aqueous mixture comprising a resinous binding agent, whereby to form an aqueous coating solution, the ratio of zinc oxide to the total quantity of resin encapsulant and said resinous binding agent in said coating solution being within a range of about 2 to 3:1, by weight,
- a method of forming a photoconductive layer on a substrate of an electrophotographic recording element comprising mixing together in a homogeneous mixture photoconductive zinc oxide particles, at least one water soluble light-sensitizing dye, a resin substantially insoluble in water, and a solvent for said resin,
- a method of forming a photoconductive layer on a substrate of an electrophotographic recording element comprising making a homogeneous mixture of resin-encapsulated dye sensitized zinc oxide particles dispersed in an aqueous mixture comprising a resinous binding agent, whereby to form an aqueous coating solution, flow coating said coating solution on said substrate to coat said substrate, whereby to form said photoconductive layer thereon, and drying said substrate and said photoconductive layer thereon, said particles comprising a core of photoconductive zinc oxide, at least one water soluble light-sensitizing dye adsorbed to said core, and a substantially water insoluble resin encapsulating said dyed core.
- a method of forming a photoconductive layer on a substrate of an electrophotographic recording element comprising mixing together in a homogeneous mixture photoconductive zinc oxide, at least one water soluble lightsensitizing dye, a resin substantially insoluble in water, and a solvent for said resin, spray drying said homogeneous mixture whereby to form particles of resin-encapsulated, dyed, photoconductive Zinc oxide, the ratio of said zinc oxide to said resin being in the range between 2 and 7.5 :1 by weight, dispersing said particles of resin-encapsulated dyed photoconductive zinc oxide in an aqueous mixture comprising a resinous binding agent, whereby to form a homogeneous aqueous coating solution, applying said coating solution to said substrate to coat said substrate, whereby to form said photoconductive layer thereon, and heating said photoconductive layer to fuse said resinencapsulated particles 'with said resinous binding agent.
- a method of forming a photoconductive layer on a substrate of an electrophotoi'graphic recording element comprising making a homogeneous mixture of resin encapsulated dye-sensitized zinc oxide particles dispersed in an aqueous mixture comprising a resinous binding agent, whereby to form an aqueous coating solution, flow coating said coating solution on said substrate to coat said substrate, whereby to form said photoconductive layer thereon, drying said substrate and said photoconductive layer thereon, said particles comprising a core of photoconductive zinc oxide, at least one water soluble light-sensitizing dye adsorbed to said core, and a substantially water insoluble resin encapsulating said dyed core, the ratio of zinc oxide to the total quantity of resin in said coating solution being in the range of about 2 to 3: 1, by weight.
- a method of forming a photoconductive layer on a substrate of an electrophotographic recording element, from a substantially aqueous dispersion of particles wherein each particle comprises a core of zinc oxide, a water soluble dye adsorbed to said core, and a water insoluble resin encapsulating said dyed core said method comprising making a homogeneous dispersion in the proportions of 7 g. of resin-encapsulated dye-sensitized zinc oxide particles, 5 ml. of water, and 5 ml. of a homogeneous mixture of g. of a 14% acrylate polymer resin water suspension, 12.5 g. of a 14% rosin modified polyester alkali-soluble solution, 7.5 g.
- encapsulated dye-sensitized zinc oxide particles comdispersing said particles of resin encapsulated dyeprising sensitized zinc oxide in an aqueous mixture coma core of photoconductive zinc oxide, prising a resinous binding agent, whereby to form a water soluble light-sensitizing dye adsorbed thereto, an aqueous coating solution, the total quantity of and resinous binding agent in said coating solution being a substantially water insoluble resin surrounding said such as to provide, with said resin encapsulant, a dyed core. ratio of 1 part of resin to about 2 to 3 parts of zinc 13.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US42644365A | 1965-01-18 | 1965-01-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3428452A true US3428452A (en) | 1969-02-18 |
Family
ID=23690826
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US426443A Expired - Lifetime US3428452A (en) | 1965-01-18 | 1965-01-18 | Photoconductive compositions and electrophotographic recording elements made therefrom |
Country Status (7)
Country | Link |
---|---|
US (1) | US3428452A (cs) |
BE (1) | BE675211A (cs) |
DE (1) | DE1522675A1 (cs) |
FR (1) | FR1463724A (cs) |
GB (1) | GB1135373A (cs) |
NL (1) | NL6600573A (cs) |
SE (1) | SE332933B (cs) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3661572A (en) * | 1969-08-04 | 1972-05-09 | Fuji Photo Film Co Ltd | Manufacturing process for manufacturing electrophotographic sensitive material |
US4281055A (en) * | 1979-02-24 | 1981-07-28 | Konishiroku Photo Industry Co., Ltd. | Photosensitive element with water soluble interlayer |
US4308334A (en) * | 1978-01-24 | 1981-12-29 | Kinoshita Laboratory | Method of sensitizing zinc oxide with sensitizing dye and photosensitive layers utilizing the sensitized zinc oxide |
US4335195A (en) * | 1979-08-10 | 1982-06-15 | Canon Kabushiki Kaisha | Electrophotosensitive element has resin encapsulated CdS particles in binding resin |
US4435493A (en) | 1981-01-15 | 1984-03-06 | Oce-Nederland B.V. | Porous reusable ZnO electrophotographic element |
US4521503A (en) * | 1984-05-11 | 1985-06-04 | Minnesota Mining And Manufacturing Company | Highly photosensitive aqueous solvent-developable printing assembly |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2952650C2 (de) * | 1978-12-28 | 1983-08-04 | Konishiroku Photo Industry Co., Ltd., Tokyo | Eingekapselter Photoleiter |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB888371A (en) * | 1957-02-15 | 1962-01-31 | Harris Intertype Corp | Electrophotosensitive coating material and electrophotographic image carriers |
US3060021A (en) * | 1958-03-20 | 1962-10-23 | Rca Corp | Method for electrophotographically producing a multicolor picture |
US3121006A (en) * | 1957-06-26 | 1964-02-11 | Xerox Corp | Photo-active member for xerography |
US3198647A (en) * | 1961-04-19 | 1965-08-03 | Quaker Chem Corp | Treated pigments and process for modifying the surface of pigments |
US3212887A (en) * | 1961-04-07 | 1965-10-19 | Minnesota Mining & Mfg | Laterally disposed coterminously adjacent multicolor area containing graphic reproduction receptor and electrophotographic process of using same |
US3238149A (en) * | 1961-07-10 | 1966-03-01 | Method for improxvlnxg the the photocondug thqe response of dye sensitized zinc ox de |
-
1965
- 1965-01-18 US US426443A patent/US3428452A/en not_active Expired - Lifetime
-
1966
- 1966-01-12 GB GB1539/66A patent/GB1135373A/en not_active Expired
- 1966-01-14 DE DE19661522675 patent/DE1522675A1/de active Pending
- 1966-01-17 SE SE00572/66A patent/SE332933B/xx unknown
- 1966-01-17 BE BE675211D patent/BE675211A/xx unknown
- 1966-01-17 NL NL6600573A patent/NL6600573A/xx unknown
- 1966-01-18 FR FR46269A patent/FR1463724A/fr not_active Expired
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB888371A (en) * | 1957-02-15 | 1962-01-31 | Harris Intertype Corp | Electrophotosensitive coating material and electrophotographic image carriers |
US3121006A (en) * | 1957-06-26 | 1964-02-11 | Xerox Corp | Photo-active member for xerography |
US3060021A (en) * | 1958-03-20 | 1962-10-23 | Rca Corp | Method for electrophotographically producing a multicolor picture |
US3212887A (en) * | 1961-04-07 | 1965-10-19 | Minnesota Mining & Mfg | Laterally disposed coterminously adjacent multicolor area containing graphic reproduction receptor and electrophotographic process of using same |
US3198647A (en) * | 1961-04-19 | 1965-08-03 | Quaker Chem Corp | Treated pigments and process for modifying the surface of pigments |
US3238149A (en) * | 1961-07-10 | 1966-03-01 | Method for improxvlnxg the the photocondug thqe response of dye sensitized zinc ox de |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3661572A (en) * | 1969-08-04 | 1972-05-09 | Fuji Photo Film Co Ltd | Manufacturing process for manufacturing electrophotographic sensitive material |
US4308334A (en) * | 1978-01-24 | 1981-12-29 | Kinoshita Laboratory | Method of sensitizing zinc oxide with sensitizing dye and photosensitive layers utilizing the sensitized zinc oxide |
US4281055A (en) * | 1979-02-24 | 1981-07-28 | Konishiroku Photo Industry Co., Ltd. | Photosensitive element with water soluble interlayer |
US4335195A (en) * | 1979-08-10 | 1982-06-15 | Canon Kabushiki Kaisha | Electrophotosensitive element has resin encapsulated CdS particles in binding resin |
US4435493A (en) | 1981-01-15 | 1984-03-06 | Oce-Nederland B.V. | Porous reusable ZnO electrophotographic element |
US4521503A (en) * | 1984-05-11 | 1985-06-04 | Minnesota Mining And Manufacturing Company | Highly photosensitive aqueous solvent-developable printing assembly |
Also Published As
Publication number | Publication date |
---|---|
NL6600573A (cs) | 1966-07-19 |
GB1135373A (en) | 1968-12-04 |
DE1522675A1 (de) | 1969-10-16 |
SE332933B (cs) | 1971-02-22 |
BE675211A (cs) | 1966-05-16 |
FR1463724A (fr) | 1966-12-23 |
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