US3554746A - Photoconductive elements containing haloarylketone-formaldehyde polymeric binders - Google Patents

Photoconductive elements containing haloarylketone-formaldehyde polymeric binders Download PDF

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US3554746A
US3554746A US814202A US3554746DA US3554746A US 3554746 A US3554746 A US 3554746A US 814202 A US814202 A US 814202A US 3554746D A US3554746D A US 3554746DA US 3554746 A US3554746 A US 3554746A
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Stewart H Merrill
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Eastman Kodak Co
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    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—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
    • G03G5/0528—Macromolecular bonding materials
    • G03G5/0557—Macromolecular bonding materials obtained otherwise than by reactions only involving carbon-to-carbon unsatured bonds
    • G03G5/0567—Other polycondensates comprising oxygen atoms in the main chain; Phenol resins

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  • This invention relates to novel electrophotographic elements having coatings of binder-containing photoconductive compositions.
  • Binder-containing photoconductive compositions have been widely used in the preparation of electrophotographic elements. In electrophotographic reproduction process, these elements are utilized in the formation of latent electrostatic images.
  • the photoconductive compositions contain an organic photoconductor and a sensitized uniformly admixed in an inert resinous binder.
  • Many binders are currently used in connection with a wide variety of available organic photoconductor compounds and compositions. Typical binders are ordinary polymeric materials, e.g., phenolic resins, acrylic ester resins, polystyrene, etc. However, these binders usually do not impart any particular improvement in light sensitivity to the system.
  • an electrophotographic element having coated thereon a photoconductive composition which contains a photoconductor admixed with a binder which is a halorylketone-formaldehyde resin.
  • such terms refer to related curves resulting from exposure plotted against voltage.
  • the reduction of the surface potential to 100 volts or below is significant in that it represents a requirement for suitable broad area development of an electrostatic image.
  • the realtive speed at 100 volts is a meaure of the ability to produce and henceforth to develop or otherwise utilize the electrostatic latent image.
  • the surface potential does not drop to or below 100 vots and therefore no speed can be assigned to such a composition.
  • a photoconductor is part of the coating in many conventional polymeric binders, the surface potentials of such resultant compositions usually drop below 100 volts, and thus, a definite speed can be ascertained. However, these speeds are improved when the binders of this invention are employed.
  • the aryl nucleus of the novel haloarylketone-formaldehyde resinous binders of this invention is substituted in either the ortho, meta or para position (with respect to the -carboyl grouping) by any of the halogens including chlorine, bromine, iodine and fluorine.
  • the aryl nucleus can contain further substitution including one or more additional halogen atoms, an alkyl group having 1 to 10 carbon atoms including an aliphatic alkyl group as well as a cycloalkyl group, an aryl group such as phenyl or naphthyl, an amino group including a substituted amino group such as dialkylamino group, a hydroxy group, etc. Binders comprising such polymers improve the electrical speed of the phtoconductive composition.
  • Particularly useful binders of this invention comprise polymers which contain the repeating unit wherein X is a halo-substituted aryl group such as halophenyl,
  • halonaphthyl e.g., p-chlorophenyl, 3,4-dichlorophenyl, 3-methyl-4-chlorophenyl, 3-phenyl-4-bromophenyl, 3 diethylamino 4 bromophenyl, 3 chloro 4 hydroxyphenyl, 3 cyclohexyl 4 chlorophenyl, and
  • R is either (1) an alkyl group having 1 to 4 carbon atoms including substituted alkyl groups such as haloalkyl, aralkyl, etc., e.g., methyl, ethyl, propyl, butyl, isopropyl, chloromethyl, trifluoromethyl, benzyl, cyclobutyl, etc., (2) hydrogen or (3) an aryl radical including a substituted aryl radical such as alkaryl, haloaryl, etc., e.g., phenyl, naphthyl, bromophenyl, tolyl, dichloronaphthyl, trimethylphenyl, etc.
  • substituted alkyl groups such as haloalkyl, aralkyl, etc., e.g., methyl, ethyl, propyl, butyl, isopropyl, chloromethyl, trifluoromethyl, benzyl, cyclobutyl, etc.
  • novel binders of this invention improve the electrical speeds of compositions containing a wide variety of photoconductors including inorganic photoconductors such as zinc oxide, titanium dioxide, cadmium sulfide and the like and organic photoconductors including organometallic photoconductors.
  • photoconductors including inorganic photoconductors such as zinc oxide, titanium dioxide, cadmium sulfide and the like and organic photoconductors including organometallic photoconductors.
  • Arylamine photoconductors including substituted and unsubstituted arylamines, diarylamines, nonpolymeric triarylamines and polymeric triarylamines such as those described in US. Pats. 3,240,597 and 3,180,730.
  • each of D, E and G is an aryl group and J is a hydrogen atom, an alkyl group, or an aryl group, at least one of D, E and G containing an amino substituent, the aryl groups attached to the central carbon atom being preferably phenyl groups, although naphthyl groups can also be used including substituted aryl groups containing substituents such as alkyl and alkoxy typically having 1 to 8 carbon atoms, hydroxy, halogen, etc.
  • each R can be an alkyl group typically having 1 to 8 carbon atoms, a hydrogen atom, an aryl group, or together the necessary atoms to form a heterocyclic amino group typically having 5 to 6 atoms in the ring such as moropholino, pyridyl, pyrryl, etc.; at least one of D, E and G preferably being a p-dialkylaminophenyl group, when I is an alkyl group, such an alkyl group more generally has 1 to 7 carbon atoms, these materials being more fully described in US. Pat. 3,274,000, French Pat. 1,383,461 and in US. Ser. No. 627,857, filed Apr. 3, 1967 by Seus and Goldman.
  • R and R are each phenyl radicals including substituted phenyl radicals, R preferably having the formula wherein R and R are each aryl radicals, aliphatic residues of l to 12 carbon atoms such as alkyl radicals preferably having 1 to 4 carbon atoms, or hydrogen; particularly advantageous results being obtained when R is a phenyl radical including a substituted phenyl radical and where R is diphenylaminophenyh, dimethylaminophenyl or phenyl, these materials being more fully described in Fox application U.S. Ser. No. 613,846.
  • Non-ionic cycloheptenyl compounds which may be substituted with substituents such as ,(a) an aryl radical including substituted as well as unsubstituted aryl radicals, (b) a hydroxy radical, (c) an azido radical, (d) a heterocyclic radical having 5 to 6 atoms in the heterocyclic nucleus and at least one hetero nitrogen atom, and including substituted and unsubstituted heterocyclic radicals, and (e) an oxygen linked cycloheptenyl moiety.
  • substituents such as ,(a) an aryl radical including substituted as well as unsubstituted aryl radicals, (b) a hydroxy radical, (c) an azido radical, (d) a heterocyclic radical having 5 to 6 atoms in the heterocyclic nucleus and at least one hetero nitrogen atom, and including substituted and unsubstituted heterocyclic radicals, and (e) an oxygen linked cyclohepten
  • E and G can be either:
  • D can be any of the substituents defined for E and 6,, above and is attached to a carbon atom in the cycloheptenyl nucleus having a double bond; (R and R (R and R (R and R and (R and R are together the necessary atoms to complete a benzene ring fused to the cycloheptenyl nucleus; these compounds being more fully described in U.S. Ser. No. 654,091 filed July 18, 1967.
  • a phenyl radical including a substituted phenyl radical such as a naphthyl, an aminophenyl or a hydroxyphenyl radical,
  • an amino radical including substituted as well as unsubstituted amino radicals such as an alkylamino or a phenylalkylamino radical,
  • a heterocyclic radical such as a pyrazolyl, a carbazolyl or a pyridyl radical
  • tetra-substituted hydrazines containing substituents which are substituted or unsubstituted phenyl radicals, or heterocyclic radicals having 5 to 6 atoms in the hetero nucleus, suitable results being obtainedwhen all four substituents are not unsubstituted phenyl radicals, i.e., if at least one substituent is a substituted phenyl radical or a heterocyclic radical having 5 to 6 atoms in the hetero nucleus.
  • Other tetra-substituted hydrazines include those having the following formula:
  • D E G and I are each either (a) a substituted phenyl radical such as a naphthyl radical, an alkylphenyl radical, a halophenyl radical, a hydroxyphenyl radical, a haloalkylphenyl radical or a hydroxyalklphenyl radical or (b) a heterocclic radical such as an imidazolyl radical, a
  • furyl radical or a pyrazolyl radical can also be ,(c) an unsubstituted phenyl radical.
  • Especially preferred are those tetra-substituted hydrazines wherein both D and G are either substituted phenyl radicals or heterocyclic radicals.
  • (G) Organic compounds having a 3,3'-bis-aryl-2-pyrazoline nucleus which is substituted in either five-member ring with the same or difierent substituents.
  • the 1 and 5 positions on both pyrazoline rings can be substituted by an aryl moiety including unsubstituted as well as substituted aryl substituents such as alkoxyaryl, alkaryl, alkaminoaryl, carboxyaryl, hydroxyaryl and haloaryl.
  • the 4 position can contain hydrogen or unsubstituted as well as substituted alkyl and aryl radicals such as alkoxyaryl, alkaryl, alkaminoaryl, haloaryl, hydroxyaryl, alkoxyalkyl, amonoalkyl, carboxylaryl, hydroxyalkyl and haloalkyl.
  • D D' I and J can be either a phenyl radical including a substituted phenyl radical such as a tolyl radical or a naphthyl radical including a substituted naphthyl radical,
  • E E G G' L and U can be any of the substituents set forth above and in addition can be either a hydrogen atom or an alkyl radical containing 1-8 carbon atoms.
  • Groups which contain active hydrogen are well known in the art, the definitions of this term being set forth in several textbooks such as Advanced Organic Chemistry, R. C. Fuson, pp. 154-157, John Wiley & Sons, 1950.
  • active hydrogen-containing group includes those compounds encompassed by the discussion in the textbook cited above and in addition includes those compounds which contain groups which are hydrolyzable to active hydrogen-containing groups.
  • Typical active hydrogen-containing groups substituted on the vinylene radical of the triarylamine include:
  • R is alkyl or aryl
  • R is alkyl or aryl
  • cyclic ester radicals e.g.,
  • R is a cyclic alkylene radical connected to a vinylene combination such as is found' in coumarin derivatives
  • amido radicals e.g., N-(2-aminoethyl)-2-aminoethyl radicals
  • R is a hydrogen atom, an alkyl group or an aryl group).
  • active hydrogen-containing groups include substituted and unsubstituted alkylidyne oximido radicals.
  • Photoconductors included in this class can be represented by the following structure:
  • Ar and Ar are each a phenyl radical including a substituted phenyl radical such as a halophenyl radical, an alkyl phenyl radical or an aminophenyl radical;
  • Ar is an arylene radical including a substituted arylene radical such as a phenylene radical or a naphthylene radical,
  • R and R are each hydrogen, a phenyl radical including a substituted phenyl radical or a lower alkyl radical preferably having 1-8 carbon atoms;
  • X is either (1) an active hydrogen-containing group such as a carboxy radical, an acyl halide radical, an amido radical, a carboxylic acid anhydride radical, an ester radical, a cyano radical, a hydroxy radical, a semicarbazono radical, an ethynyl radical, or a methylidyne oximido radical, or (2) hydrogen, provided that when X is hydrogen R and R are also hydrogen; and
  • n is an integer of one to three.
  • the arylene nucleus can be substituted in any position by the vinyl or vinylene moiety.
  • Ar is phenylene, particularly good results are obtained if the substitution occurs in the para position.
  • Triarylamines in which at least one of the aryl radicals is substituted by an active hydrogen-containing group.
  • active hydrogen-containing group has the same meaning as set forth above and again includes those compounds encompassed by the discussion in the textbook and additionally includes those compounds which contain groups which are hydrolyzable to active hydrogen-containing groups.
  • Typical active hydrogen-containing groups which are substituted on an aryl radical of the triaryl- 4 amine include:
  • Rm wherein R is a hydrogen atom, an alkyl group or an y p);
  • arylene carboxy radicals including substituted arylene carboxy radicals e.g.,
  • D and E are phenyl or lower alkyl radicals.
  • Photoconductors included in this class can be represented by the following structure:
  • Ar are each a phenyl radical including a substituted phenyl radical such as a halophenyl radical, an alkyl phenyl radical or an amino phenyl radical;
  • Ar is an arylene radical including a substituted arylene radical such as a phenylene radical or a naphthylene radical;
  • X is an active hydrogen-containing group such as a carboxy radical, an acyl halide radical, an amido radical, a carboxylic acid anhydride radical, an ester radical, a cyano radical, a semicarbazono radical, a hydroxy radical, an ethynyl radical, a methylidyne oximido radical or a phenylene carboxy radical.
  • the metallic substituents of this class of organic photoconductors are Group IVa or Group Va metals in accordance with the Periodic Table of the Elemerits (Handbook of Chemistry and Physics, 38 edition, pp. 394-) and include silicon, germanium, tin and lead from Group IVa and phosphorus, arsenic, antimony and and bismuth from Group Va. These materials can be substituted in the metallo nucleus with a wide variety of substituents but at least one of the substituents must be an amino-aryl radical.
  • the amino radical can be positioned anywhere on the aromatic nucleus, but best results are obtained if the aryl moiety is a phenyl radical having the amino group in the 4 or para position.
  • Typical substituents attached to the metal nucleus include the following:
  • Photoconductors included in this class can be represented by the following structures:
  • E G L and Q can be (a) a hydrogen atom
  • an aryl radical including unsubstituted as well as substituted aryl radicals such as a phenyl radical, a naphthyl radical, a dialkylaminophenyl radical, or a diarylaminophenyl radical,
  • R and R can be hydrogen atoms or alkyl radicals having 1 to 8 carbon atoms, or (g) a heterocyclic radical having 5 to 6 atoms in the hetero nucleus including at least one nitrogen atom such as a triazolyl, a pyridyl radical, etc.;
  • T is an amino radical such as an alkylamino radical having 1 to 8 carbon atoms or an arylamino radical such as a phenylamino radical;
  • Ar is an aromatic radical such as phenyl or naphthyl
  • M and M are the same or diiferent Group IVa metals
  • M is a Group Va metal
  • D can be any of the substituents set forth above for E G L and Q and in addition can be a Group IVa organo-metallic radical or when taken with B, an oxygen atom or a sulfur atom;
  • E G L and Q can be any of the substituents set forth above for E G L and Q and in addition can be when taken with E, an oxygen atom or a sulfur atom. These materials are described in US. Ser. No. 650,664, filed July 3, 1967.
  • organic photoconductors useful in this invention include the compounds listed below:
  • Sensitizing compounds useful with the photoconductive compounds of the present invention can be selected from a wide variety of materials, including such materials as pyrylium including thiapyrylium and selenapyrylium dye salts disclosed in Van Allan et al. US. Pat. 3,250,615; fiuorenes, such as 7,12-dioxo-13-dibenzo(a,h) fiuorene, 5,15-dioxo4a,11-diazabenzo(b)fluorene, 3,13- dioxo-7-oxadibenzo(b,g)fluorene, and the like; aromatic nitro compounds of the kinds described in US. Pat.
  • 2,732,301 mineral acids
  • carboxylic acids such as maleic acid, dichloroacetic acid, and salicyclic acid
  • sulfonic and phosphoric acids such as cyanine (including cartbocyanine), merocyanine, diarylmethane, thiazine, azine, oxazine, xanthene, phthalein, acridine, azo, anthraquinone dyes and the like and mixtures thereof.
  • the sensitizers preferred for use with the compounds of this invention are selected from pyrylium salts including selenapyrylium and thiapyrylium salts, and cyanine dyes including carbocyanine dyes.
  • sensitizing compound is employed with the binder and organic photoconductor to form a sensitized electrophotographic element
  • Other methods of incorporating the sensitizer or the effect of the sensitizer may, however, be employed consistent with the practice of this invention.
  • the sensitizer is preferred.
  • the amount of sensitizer that can be added to a photoconductor-incorporating layer to give elfective increases in speed can vary widely. The optimum concentration in any given case will vary with the specific photoconductor and sensitizing compound used. In general, substantial speed gains can be obtained where an appropriate sensitizer is added in a concentration range from about 0.0001 to about 30 percent by weight based on the weight of the film-forming coating composition. Normally, a sensitizer is added to the coating composition in an amount by weight from about 0.005 to about 5.0 percent by weight ofthe total coating composition.
  • ISolvents useful for preparing coating compositions with the binders of the present invention can include a wide variety of organic solvents for the components of the coating composition.
  • organic solvents for the components of the coating composition.
  • benzene; toluene; acetone; Z-butanone; chlorinated hydrocarbons such as methylene chloride; ethylene chloride; and the like; ethers, such as tetrahydrofuran and the like, or mixtures of such solvents can advantageously be employed in the practice of this invention.
  • the photoconductive substance is present in an amount equal to at least about 1 weight percent of the coating composition.
  • the upper limit in the amount of photoconductive material present can be widely varied in accordance with usual practice. It is normally required that the photoconductive material be present in an amount ranging from about 1 weight percent of the coating composition to about 99 weight percent of the coating composition.
  • a preferred weight range for the photoconductive material in the coating composition is from about weight percent to about 60 weight percent.
  • Coating thicknesses of the photoconductive composition on a support can vary widely. Normally, a wet coating thickness in the [range of about 0.001 inch to about 0.01 inch is useful in the practice of the invention. A preferred range of coating thickness is from about 0.002 inch to about 0.006 inch before drying although such thicknesses can vary widely depending on the particular application desired for the electrophotographic element.
  • Suitable supporting materials for coating the photoconductive layers of the present invention can include any of the electrically conducting supports, for example, paper (at relative humidity above 20 percent); aluminum-paper laminates; metal foils, such as aluminum foil, zinc foil, etc.; metal plates, such as aluminum, copper, zinc, brass, and galvanized plates; vapor deposited metal layers such as silver, nickel or aluminum on conventional film supports such as cellulose acetate, poly(ethylene terephthalate), polystyrene and the like conducting supports.
  • the electrically conducting supports for example, paper (at relative humidity above 20 percent); aluminum-paper laminates; metal foils, such as aluminum foil, zinc foil, etc.; metal plates, such as aluminum, copper, zinc, brass, and galvanized plates; vapor deposited metal layers such as silver, nickel or aluminum on conventional film supports such as cellulose acetate, poly(ethylene terephthalate), polystyrene and the like conducting supports.
  • An especially useful conducting support can be prepared by coating a transparent film support material such as poly(ethylene terephthalate) with a layer containing a semiconductor dispersed in a resin.
  • a suitable conducting coating can be prepared from the sodium salt of a carboxyester lactone of a maleic anhydride-vinyl acetate copolymer, cuprous iodide and the like.
  • compositions of the present invention can be employed in photoconductive elements useful in any of the well known electrophotographic processes which require photoconductive layers.
  • One such process is the xerographic process.
  • an electrophotographic element held in the dark is given a blanket electrostatic charge by placing it under a corona discharge to give a uniform charge to the surface of the photoconductive layer. This charge is retained by the layer owing to the substantial dark insulating property of the layer, i.e., the low conductivity of the layer in the dark.
  • the electrostatic charge formed on the surface of the photoconductive layer is then selectively dissipated from the surface of the layer by imagewise exposure to light by meansof a conventional exposure operation such as for example, by a contact-printing technique, or by lens projection of an image, or reflex or bireflex techniques and the like, to thereby form a latent electrostatic image in the photoconductive layer.
  • Exposing the surface in this manner forms a pattern of electrostatic charge by virtue of the fact that light energy striking the photoconductor causes the electrostatic charge in the light struck areas to be conducted away from the surface in proportion to the intensity of the illumination in a particular area.
  • the charge pattern produced by exposure is then developed or transferred to another surface and developed there, i.e., either the charge or uncharged areas rendered visible, by treatment with a medium comprising electrostatically responsive particles having optical density.
  • the developing electrostatically responsive particles can be in the form of a dust, or powder and generally comprise a pigment in a resinous carrier called a toner.
  • a preferred method of applying such a toner to a latent electrostatic image for solid area development is by the use of a magnetic brush. Methods of forming and using a magnetic brush toner applicator are described in the following U.S.
  • Heating the powder image then causes the resin to melt or fuse into or on the element.
  • the powder is, therefore, caused to adhere penmanently to the surface of the photoconductive layer.
  • a transfer of the charge image or powder image formed on the photoconductive layer can be made to a second support such as paper which would then become the final print after developing and fusing or fusing respectively.
  • Techniques of the type indicated are well known in the art and have been described in a number of U.S. and foreign patents, such as U.S. Pats. 2,297,691 and 2,551,582, and in RCA Review, vol. 15 (1954) pages 469-484.
  • compositions of the present invention can be used in electrophotographic elements having many structural variations.
  • the photoconductive composition can be coated in the form of single layers or multiple layers on a suitable opaque or transparent conducting support.
  • the layers can be contiguous or spaced having layers of insulating material or other photoconductive material between layers or overcoated or interposed between the photoconductive layer or sensitizing layer and the conducting layer. It is also possible to adjust the position of the support and the conducting layer by placing a photoconductor layer over a support and coating the exposed face of the support or the exposed or overcoated face of the photoconductor with a conducting layer. Configurations differing from those contained in the examples can be useful or even preferred for the same or different application for the electrophotographic element. 9
  • EXAMPLE 1 1.5 grams of p-bromacetophenone-formaldehyde resin binder containing 0.5 gram of 4,4-benzylidene-bis(N,N- diethyl-m-toluidine) photoconductor and .04 gram of 2,4- bis-(4-ethoxyphenyl) 6 (4-n-amyloxystyryl)pyrylium fluoroborate sensitizer are dissolved in 15.6 grams of methylene chloride by stirring the solids in the solvent for one hour at room temperature. The resulting solution is hand coated at a wet coating thickness of 0.004 inch on a conducting layer comprising the sodium salt of a carboxyester lactone, such as described in U.S.
  • the electrophotographic element is charged under positive corona source until the surface potential, as measured by an electrometer probe, reaches about 600 volts. It is then subjected to exposure from behind a stepped density gray scale to a 3000 K. tungsten source. The exposure causes reduction of the surface potential of the element under each step of the gray scale from its initial potential, V to some lower potential, V, whose exact value depends on the actual amount of exposure in meter-candle-seconds received by the area. The results of the measurements are plotted on a graph of surface potential V vs. log exposure for each step.
  • the shoulder speed is the numerical expression of multiplied by the reciprocal of the exposure in meter-candle-seconds required to reduce the 600 volt charged surface potential by 100 volts.
  • the toe speedm is the numerical expression of 10 multiplied by the reciprocal of the exposure in meter-candle-seconds required to reduce the 600 volt charged surface potential to 100 volts. This coating is found to have a positive 100 v. toe speed of 250 and a shoulder speed of 1800.
  • Example 1 is repeated except that the element is charged under a negative corona source until the surface potential reaches about 600 volts (negative).
  • the shoulder and 100 volt toe speeds are determined in the same manner as Example 1. In this case, the negative shoulder speed is 1400 and the negative 100 volt toe speed is 120.
  • EXAMPLE 3 For comparison purposes, Examples 1 and 2 are repeated except that the binder used is an unhalogenated acetophenoneformaldehyde resin.
  • the positive shoulder speed is 1000 and the positive 100 volt toe speed is 45.
  • the negative shoulder speed is 1200 while the negative 100 volt tOe speed is 32.
  • the halogenated arylketone-formaldehyde resins exhibited substantially higher speeds than the unhalogenated resins.
  • EXAMPLE 4 Coating compositions containing Compounds 1 through 8 are prepared and coated in the manner described in Example I.
  • the surface of each of the photoconductive layers so prepared is charged ,to a potential of about +600 volts under a corona charger.
  • the layer is then covered with a transparent sheet bearing a pattern of opaque and light transmitting areas and exposed to the radiation from an incandescent lamp with an illumination intensity of about 75 meter-candles for 12 seconds.
  • the resulting electrostatic latent image is developed in the usual manner by cascading over the surface of the layer a mixture of negatively charged black thermoplastic toner particles and glass beads. A good reproduction of the pattern results in each instance.
  • haloarylketone-formaldehyde resins useful as binders for electrophotographic compositions and elements of this invention are prepared by methods known to those skilled in the art. Generally, the appropriate haloarylketone is condensed with formaldehyde. A typical preparation is set forth below.
  • EXAMPLE 5 0.6 gram of sodium hydroxide is added to a mixture of 100 g. (.50 mole) of p-bromoacetophenone and 60 g. (.75 mole) of 35-40% aqueous formaldehyde in 400 ml. of ethanol. The mixture is stirred at reflux for minutes after which the supernatant liquid is decanted from the viscous liquid. The resin is Washed by stirring at reflux with 200 ml. of 2:1 ethanol-water for 30 minutes. After decanting the liquid, the washing operation is repeated. The resin is cooled, ground and dried. Approximately grams of p-bromoacetophenoneformaldehyde resin are recovered.
  • An electrophotographic element comprising a support having coated thereon a photoconductive composi tion comprising a photoconductor and a binder comprising a haloarylketone-formaldehyde resin.
  • An electrophotographic element comprising a support having coated thereon a photoconductive composition comprising an organic photoconductor and a binder comprising a resin having repeated units represented by the following structure:
  • X is a halo-substituted aryl group and R is selected from the group consisting of an aryl group,
  • sensitizer is selected from the group consisting of cyanine and pyrylium dye salts.
  • the electrophotographic element of claim 3 wherein the organic photoconductor is 4,4'-benzylidenebis-(N,N- diethyl-m-toluidine) 11.
  • An electrophotographic element comprising a support having coated thereon a photoconductive composition comprising from about 1 0 to about 60 weight percent of 4,4'-'benzylidenebis-(N,N-diethyl-m-toluidine) as an organic photoconductor, 0.005 to about 5.0 weight percent of a sensitizer for said photoconductor and a p-bromoacetophenone-formaldehyde resin binder.
  • An electrophotographic element comprising a support having coated thereon a photoconductive composition comprising from about 10 to about 60 weight percent of 4,4-benzylidenebis-(N,N-diethyl-m-toluidine) as an organic photoconductor, 0.005 to about 5.0 weight percent 17 of a sensitizer for said photoconductor and a m-chloroacetophenone-formaldehyde resin.
  • An electrophotographic element comprising a support having coated thereon a photoconductive composition comprising from about 10 to about 60 weight percent of 4,4-benzylidenebis-(N,N-diethyl-m-toluidine) as an organic photoconductor, 0.005 to about 5.0 weight percent of a sensitizer for said photoconductor and a p-chloroacetophenone-formaldehyde resin binder.
  • An electrophotographic element comprising a support having coated thereon a photoconductive composition comprising from about 10 to about 60 weight percent of 4,4-benzylidenebis-(N,N-diethyl-m-toluidine) as an organic photoconductor, 0.005 to about 5.0 weight percent of a sensitizer for said photoconductor and a 3,4'-dichloroacetophenoneformaldehyde resin binder.
  • an electrophotographic process wherein an electrostatic charge pattern is formed on a photoconductive element, the improvement characterized in that said photoconductive element has a photoconductive layer comprising an organic photoconductor and a haloarylketoneformaldehyde resin binder.
  • a photoconductive composition comprising a photoconductor and a haloarylketone-formaldehyde resin binder.
  • a photoconductive composition comprising an organic photoconductor and a binder comprising a resin having repeating units represented by the following structure:

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DE (1) DE2016395C3 (enrdf_load_stackoverflow)
FR (1) FR2042976A5 (enrdf_load_stackoverflow)
GB (1) GB1283652A (enrdf_load_stackoverflow)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3943108A (en) * 1974-09-27 1976-03-09 Xerox Corporation Photoconductive composition of an aldehyde condensate
US4792511A (en) * 1986-03-14 1988-12-20 Fuji Photo Film Co., Ltd. Electrophotographic zinc oxide-resin binder lithographic printing plate precursor
US5362167A (en) * 1991-12-18 1994-11-08 The Gillette Company Fiber marker including an erasable ink
US5599853A (en) * 1993-01-29 1997-02-04 The Gillette Company Erasable inks

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63180197U (enrdf_load_stackoverflow) * 1987-05-08 1988-11-21

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3943108A (en) * 1974-09-27 1976-03-09 Xerox Corporation Photoconductive composition of an aldehyde condensate
US4792511A (en) * 1986-03-14 1988-12-20 Fuji Photo Film Co., Ltd. Electrophotographic zinc oxide-resin binder lithographic printing plate precursor
US5362167A (en) * 1991-12-18 1994-11-08 The Gillette Company Fiber marker including an erasable ink
US5919858A (en) * 1991-12-18 1999-07-06 The Gillette Company Erasable inks
US5599853A (en) * 1993-01-29 1997-02-04 The Gillette Company Erasable inks

Also Published As

Publication number Publication date
JPS4843827B1 (enrdf_load_stackoverflow) 1973-12-20
CA919479A (en) 1973-01-23
DE2016395A1 (de) 1970-10-15
GB1283652A (en) 1972-08-02
DE2016395C3 (de) 1974-09-05
DE2016395B2 (de) 1974-02-14
FR2042976A5 (enrdf_load_stackoverflow) 1971-02-12
BE748511A (fr) 1970-09-16

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