US3674711A - Electrically conductive transparent plastic material - Google Patents
Electrically conductive transparent plastic material Download PDFInfo
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- US3674711A US3674711A US883732A US3674711DA US3674711A US 3674711 A US3674711 A US 3674711A US 883732 A US883732 A US 883732A US 3674711D A US3674711D A US 3674711DA US 3674711 A US3674711 A US 3674711A
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- 239000000463 material Substances 0.000 title abstract description 11
- 229920003023 plastic Polymers 0.000 title abstract description 11
- 229920000642 polymer Polymers 0.000 claims abstract description 32
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 13
- 229920001940 conductive polymer Polymers 0.000 abstract description 16
- 239000002904 solvent Substances 0.000 abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 9
- 239000011248 coating agent Substances 0.000 abstract description 7
- 238000000576 coating method Methods 0.000 abstract description 7
- PZNOBXVHZYGUEX-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine;hydrochloride Chemical compound Cl.C=CCNCC=C PZNOBXVHZYGUEX-UHFFFAOYSA-N 0.000 abstract description 7
- 229920000867 polyelectrolyte Polymers 0.000 abstract description 7
- 239000004033 plastic Substances 0.000 abstract description 6
- 239000002985 plastic film Substances 0.000 abstract description 6
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract description 6
- 238000005266 casting Methods 0.000 abstract description 5
- 239000007787 solid Substances 0.000 abstract description 3
- 239000010408 film Substances 0.000 description 29
- -1 for example Substances 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 13
- 239000000758 substrate Substances 0.000 description 13
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 6
- 229920001519 homopolymer Polymers 0.000 description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229920001756 Polyvinyl chloride acetate Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- LZBCVRCTAYKYHR-UHFFFAOYSA-N acetic acid;chloroethene Chemical compound ClC=C.CC(O)=O LZBCVRCTAYKYHR-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000004350 aryl cycloalkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000000332 continued effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/122—Ionic conductors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/15—Antistatic agents not otherwise provided for
- Y10S260/17—High polymeric, resinous, antistatic agents
- Y10S260/18—High polymeric, resinous, antistatic agents containing pentavalent nitrogen
Definitions
- An electrically conductive clear transparent self-supporting plastic sheet consisting of a homogeneous solid molecular mixture of a clear transparent conductive polymer and a film forming clear transparent polymer is obtained by combining a quaternary ammonium polyelectrolyte, such as polydimethyl diallyl ammonium chloride, with a film forming polymer, such as polyvinyl alcohol, and a mutual solvent, such as water.
- a quaternary ammonium polyelectrolyte such as polydimethyl diallyl ammonium chloride
- a film forming polymer such as polyvinyl alcohol
- a mutual solvent such as water.
- the mixture is then cast onto a smooth surface, the mutual solvent evaporated, and the resultant sheet material stripped from the casting surface to obtain a sheet of electrically conductive clear transparent plastic material useful as a conductive plastic or, after coating with a charge retentive film, as an electrographic recording medium.
- electrically conductive transparent films have been prepared by combining a film forming polymer, a plasticizcr for the polymer, an electrolyte soluble in the plasticizer, and a solvent for the polymer and casting the resultant mixture on a casting surface to provide a selfsupporting, transparent, electrically conductive film.
- An example of such prior art is disclosed in U. S. Pat. No. 3,357,930 issued Dec. 12, 1967.
- electrolytes including acids, bases, or salts could be employed, provided that the electrolyte was soluble in the plasticizer.
- conductive films formed according to the aforecited prior art do not appear to have the requisite stability when employed as the conductive substrate for a clear transparent charge retentive film of an electrographic recording web.
- the principal object of the present invention is the provision of an improved electrically conductive transparent plastic material which is perfectly colorless or non-light absorbing.
- One feature of the present invention is the provision of a clear transparent conductive plastic material having a conductive polymer combined with a film forming polymer, whereby the improved stability of the film forming polymer is imparted to the resultant composite polmeric plastic material.
- Another feature of the present invention is the same as the preceding feature wherein the conductive polymer is a quaternary ammonium polyelectrolyte.
- Another feature of the present invention is the same as the first feature wherein the conductive polymer is polypiperidinium chloride.
- Another feature of the present invention is the same as any one or more of the preceding features including the provision of a clear non-conductive plastic charge retentive film disposed overlaying one major surface of a sheet of the conductive plastic material to form an electrographic recording web.
- FIG. 1 is a schematic flow diagram, in block diagram form, depicting the method for making conductive plastic sheet according to the present invention.
- FIG. 2 is a fragmentary perspective view, partly in section, depicting an electrographic recording web employing features of the present invention.
- FIGS. 1 and 2 there is shown in block diagram form the method for making the electrographic recording web 1 of FIG. 2 which comprises a clear, transparent, conductive sheet, as of 0.010 inch thick, having a clear, transparent, charge retentive film 3, as of 4 microns thick, adhered to the clear conductive sheet 2.
- Such an electrographic recording web is suitable for use in electrophotography to provide a transparency of photographic quality.
- a film forming polymer such as polyvinyl alcohol
- a conductive polymer such as polydimethyl diallyl ammonium chloride
- a mutual solvent for both polymers to form a clear, non-light absorbing, colorless liquid comprising a homogenous mixture of the polymers in the solvent, such as water.
- the mixture in the next step, is cast as a sheet onto a substrate to a uniform thickness, as of 0.040 inch thick.
- the solvent is evaporated to leave a clear, non-light absorptive, transparent film, as of 0.010 inch thick on the substrate,
- the film is then peeled from the substrate to produce an electrically conductive, clear, non-light absorptive transparent film which may be utilized as the clear conductive sheet 2 of the electrographic recording web I, or which may be utilized for other applications where a transparent conductive plastic sheet is desired.
- the conductive sheet 2 is coated to a thickness, as of 4 microns, with a clear charge retentive film such as of polyvinyl chloride-acetate and allowed to dry, thereby producing the electrographic recording web 1 of FIG. 2
- the film forming polymeric material useful in the practice of this invention includes a wide variety of polymers which are transparent in sheets varying from thicknesses corresponding to 0.0001 inch to 1 inch. Aside from transparency, the polymer should be castable in the form of a gel, as opposed to a hard, highly crossed linked film, so as to allow ionic mobility, and its usefulness as a film should not be effected by the con tinued presence of the solvent, for example, water in the amounts required to effect ionization of the electrolyte.
- film forming polymers particularly preferred in the practice of this invention may be mentioned those which are polymers of hydroxyl containing monomers, esters, or acetals.
- polymers include polyvinyl alcohol, agar, carboxymethylcellulose, polyvinyl acetate, polyvinyl acetate-alcohol, copolymers, polyvinyl acetal, polyvinyl formal, acrylic resins, such as polyacrylic acid, methyl cellulose, polyvinylpyrrolidone, CARBOSET 525 acrylic polymer and CARBOSET 514 acrylic polymer, the latter two being manufactured by B. F. Goodrich Chemical Company, a division of the B. F. Goodrich Company, 3135 Euclid Avenue, Cleveland 15, Ohio.
- polyvinyl alcohol may be described as a polymer of monomeric vinyl alcohol, but is invariably produced by indirect means, as vinyl alcohol is non-existent in fact.
- the conductive polymer materials useful in the practice of this invention include polymers which are transparent or nearly so in thin films.
- the conductive polymers are capable of providing both a source of ions and the necessary waterholding capacity (hygroscopicity).
- Polyelectrolytes are particularly suited for this application because of their ionic nature and ability to hold water at low humidity.
- Particularly suitable polyelectrolytes include the quaternary ammonium polyelectrolytes.
- the polymers of this type include vinylbenzyl quaternary ammonium compounds and can be any water-soluble or water-dispersible homopolymer or copolymer of one or more vinylbenzyl quaternary ammonium compounds, or copolymers of a predominant amount of vinylbenzyl quaternary ammonium compound and a minor amount of a nonacidic copolymerizable compound such as acrylamide, or copolymers containing, in the polymer molecules, residues corresponding to from 95.0 to 99.99 percent by weight of one or more vinylbenzyl quaternary ammonium compounds and from 5.0 to 0.01 percent by weight of divinyl benzene.
- the electroconductive substance can be a homopolymer or a copolymer of any two or more vinylbenzyl quaternary ammonium compounds having the general formula' wherein R, R and R" each represents individually a monovalent radical selected from the group consisting of CH OI-ICH CH CHOI-ICH CH OHCHOHCl-l and alkyl, aryl cycloalkyl and aralkyl hydrocarbon radicals, and R. R and R" collectively represent the radicals of the fonnula:
- the R groups containing a total of not more than 12 carbon atoms in the sum of the constituent radicals, or a copolymer of at least 65 percent by weight of any one or more ofsuch vinylbenzyl quaternary ammonium compounds with not more than 35 percent by weight of acrylamide, or a copolymer containing, in the polymer molecules, residues corresponding to from 95.0 to 99.99, preferably from 99.0 to 99.99 percent by weight of any one or more of such vinylbenzyl quaternary ammonium compounds and from 5.0 to 0.01, preferably from 1.0 to 0.01, percent by weight, of divinylbenzene.
- the polymers are of relatively high molecular weight and are characterized by a viscosity of at least 2 centipoises for a 0.5 percent by weight solution of the polymer in an aqueous 2 percent by weight solution of sodium chloride at 25 C. as determined by an Ostwald viscosimeter.
- the electroconductive polymer is a homopolymer or copolymer of one or more vinylbenzyl quaternary ammonium compounds having the aforementioned general formula wherein R represents an alkyl radical containing from one to four carbon atoms, R and R" each represents a radical of the group consisting or CH OHCl-l CH CHOHCH CH OHCHOHCH and lower alkyl radicals containing from 1 to 4 carbon atoms and Y is an anion, e.g., a sulfate, a chloride, a nitrate, or a hydroxyl ion, copolymers of at least 65 percent by weight of any two or more such vinylbenzyl quaternary ammonium compounds and not more than 35 percent by weight of acrylamide, or copolymers of from 99.0 to 99.99 percent by weight of at least one such vinylbenzyl quaternary ammonium compound and from 1.0 to 0.01 percent by weight of divinylbenzene.
- R represents an alkyl radical
- L H2 CH1 wherein the anion is a chloride and the polymer comprises a homopolymer of disubstituted diallyl ammonium chloride monomers where R and R are selected from the groups consisting of methyl, ethyl, and methyl, ethyl, butyl and octyl, respectively.
- R and R are selected from the groups consisting of methyl, ethyl, and methyl, ethyl, butyl and octyl, respectively.
- a particular one of the aforementioned polypiperidinium chlorides is polydimethyl diallyl ammonium chloride marketed by Calgon Corporation of Pittsburgh, Pennsylvania, as conductive polymer No. 261.
- Mutual solvents useful in the practice of this invention include water methanol-water mixtures.
- a castable composition is prepared by dissolving 15 percent by weight. polyvinyl alcohol in water.
- a suitable grade of polyvinyl alcohol is ELVANOL grade 70-05 available from E. l. DuPont de Nemours & Company, Inc., Organic Chemicals Department. This grade of polyvinyl alcohol is a hot-watersoluble grade and is slurried in cold water and then heated to complete solution. More particularly, add to the vessel the required amount of water at 75 F. or below and start agitation. Sift the polyvinyl alcohol into the vortex such that it is rapidly worked out and dispersed and stir this way for 10 minutes. Raise the temperatures to 194 F. or above and continue stirring at 194203 F.
- polydimethyl diallyl ammonium chloride (conductive polymer 261 manufactured by Calgon Corporation) in the proportions 20 parts by weight to each parts by weight of dry polyvinyl alcohol.
- the conductive polymer is preferably added in a 40 percent water solution, i.e., 40 percent by weight conductive polymer in water and stirred into the polyvinyl alcohol until dispersed uniformly therein.
- the solution is coated on a glass plate or other suitable substrate. The coating on the glass plate substrate is obtained by spreading a pool of the solution on the substrate with a glass rod to obtain a uniform thickness for the coating of approximately 0.040 inch. The coated substrate is then put in an oven at to F.
- the coating reduces to a thickness of approximately 0.010 inch.
- the coated substrate is removed from the oven and allowed to cool to room temperature. Upon cooling to room temperature, the coating is stripped or peeled from the substrate to obtain the clear, transparent, conductive plastic sheet of the present invention.
- a 25 percent solution of QX 3521 polymeric quaternary ammonia salt made by Dow Chemical Company may be substituted for polydimethyl diallyl ammonium chloride.
- the sheet 2 is perfectly clear, sufficiently flexible for further processing, and surprisingly resistant to finger marks, moisture or stickiness.
- the bulk conductivity of the sheet 2 was approximately 10 ohm centimeters when tested in ambient conditions (20 C. and 50percent relative humidity).
- the amount of conductive polymer to be employed will depend to some extent upon the degree of conductivity desired. As a general rule, however, it can be said that the amount of conductive polymer should be in the range between 5 percent and 50 percent by weight of the film forming polymer.
- the cast sheet After drying on the substrate, is coated with a dielectric charge retentive film as of vinyl chloride-acetate to a thickness as of 4 microns. If desired, the sheet 2 may be then stripped from the substrate or prepared in rolls or the like after the manner of making cellophane and similar films to provide a self-supporting, transparent electrically conductive sheet with a charge retentive film adhered thereto.
- a dielectric charge retentive film as of vinyl chloride-acetate to a thickness as of 4 microns.
- the sheet 2 may be then stripped from the substrate or prepared in rolls or the like after the manner of making cellophane and similar films to provide a self-supporting, transparent electrically conductive sheet with a charge retentive film adhered thereto.
- An electrically conductive clear transparent self-supporting plastic sheet comprising: 4
- the conductive polymer being a water-dispersible quaternary ammonium polyelectrolyte consisting of at least one member selected from the group consisting of a. homopolymers of a vinylbenzyl quaternary ammonium compound having the general formula:
- R, R and R" each represents individually a monovalent radical selected from the group consisting of CH OHCl-l CH CHOHCH CH OH-CHOHCH, and alkyl, aryl, cycloalkyl and aralkyl hydrocarbon radicals, and R, R and R" collectively represent the formula:
- copolymers of at least two such vinylbenzyl quaternary ammonium compounds b. copolymers of at least two such vinylbenzyl quaternary ammonium compounds, c. copolymers of at least 65 percent by weight of at least one of such vinylbenzyl quaternary ammonium compounds and not more than 35 percent by weight of acrylamide, and
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Abstract
An electrically conductive clear transparent self-supporting plastic sheet consisting of a homogeneous solid molecular mixture of a clear transparent conductive polymer and a film forming clear transparent polymer is obtained by combining a quaternary ammonium polyelectrolyte, such as polydimethyl diallyl ammonium chloride, with a film forming polymer, such as polyvinyl alcohol, and a mutual solvent, such as water. The mixture is then cast onto a smooth surface, the mutual solvent evaporated, and the resultant sheet material stripped from the casting surface to obtain a sheet of electrically conductive clear transparent plastic material useful as a conductive plastic or, after coating with a charge retentive film, as an electrographic recording medium.
Description
United States Patent Growald et al.
[ July4, 1972 [54] ELECTRICALLY CONDUCTIVE TRANSPARENT PLASTIC MATERIAL [731 Assignees Varian Associates, Palo Alto, Calif.
[22] Filed: Dec. 10, 1969 [2]] Appl. No.: 883,732
Marks et al ..252/50O Greer ..260/2.l E Butler et al ..260/2.l E
Primary Examiner-Douglas J. Drummond Attorney-Leon F. Herbert and Gerald L. Moore 57 ABSTRACT An electrically conductive clear transparent self-supporting plastic sheet consisting of a homogeneous solid molecular mixture of a clear transparent conductive polymer and a film forming clear transparent polymer is obtained by combining a quaternary ammonium polyelectrolyte, such as polydimethyl diallyl ammonium chloride, with a film forming polymer, such as polyvinyl alcohol, and a mutual solvent, such as water. The mixture is then cast onto a smooth surface, the mutual solvent evaporated, and the resultant sheet material stripped from the casting surface to obtain a sheet of electrically conductive clear transparent plastic material useful as a conductive plastic or, after coating with a charge retentive film, as an electrographic recording medium.
2 Claims, 2 Drawing Figures CLEAR CHARGE RETENTlVE FILM CLEAR CONDUCTIVE SHEET PATENTEBJUL '4 I872 FIG. I
COMBINING H FO CASTING EVAPORATING PEELING POLYMER AND A AS A SHEET THE OFF ON TO A MUTUAL THE MUTUAL SOLVENT SUBSTRATE SOLVENT CAST SHEET COATING THE CONDUCTIVE SHEET WITH A CLEAR CHARGE RETENTIVE FIG. 2 FILM CLEAR CHARGE RETENTIVE FILM INVENTORS BERT GROWALD JOHN A. DAHLOUIST GUY A. MARLOR BY ATTORNEY DESCRIPTION OF THE PRIOR ART Herctofore, electrically conductive transparent films have been prepared by combining a film forming polymer, a plasticizcr for the polymer, an electrolyte soluble in the plasticizer, and a solvent for the polymer and casting the resultant mixture on a casting surface to provide a selfsupporting, transparent, electrically conductive film. An example of such prior art is disclosed in U. S. Pat. No. 3,357,930 issued Dec. 12, 1967. In this prior art disclosure it was contemplated that a relatively wide range of electrolytes, including acids, bases, or salts could be employed, provided that the electrolyte was soluble in the plasticizer. However, conductive films formed according to the aforecited prior art do not appear to have the requisite stability when employed as the conductive substrate for a clear transparent charge retentive film of an electrographic recording web.
SUMMARY OF THE PRESENT INVENTION The principal object of the present invention is the provision of an improved electrically conductive transparent plastic material which is perfectly colorless or non-light absorbing.
One feature of the present invention is the provision of a clear transparent conductive plastic material having a conductive polymer combined with a film forming polymer, whereby the improved stability of the film forming polymer is imparted to the resultant composite polmeric plastic material.
Another feature of the present invention is the same as the preceding feature wherein the conductive polymer is a quaternary ammonium polyelectrolyte.
Another feature of the present invention is the same as the first feature wherein the conductive polymer is polypiperidinium chloride.
Another feature of the present invention is the same as any one or more of the preceding features including the provision of a clear non-conductive plastic charge retentive film disposed overlaying one major surface of a sheet of the conductive plastic material to form an electrographic recording web.
Other features and advantages of the present invention will become apparent upon a perusal of the following specification taken in connection with the accompanying drawings wherein:
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic flow diagram, in block diagram form, depicting the method for making conductive plastic sheet according to the present invention, and
FIG. 2 is a fragmentary perspective view, partly in section, depicting an electrographic recording web employing features of the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Referring now to FIGS. 1 and 2, there is shown in block diagram form the method for making the electrographic recording web 1 of FIG. 2 which comprises a clear, transparent, conductive sheet, as of 0.010 inch thick, having a clear, transparent, charge retentive film 3, as of 4 microns thick, adhered to the clear conductive sheet 2. Such an electrographic recording web is suitable for use in electrophotography to provide a transparency of photographic quality.
In the first step of the method, a film forming polymer, such as polyvinyl alcohol, is combined with a conductive polymer, such as polydimethyl diallyl ammonium chloride and a mutual solvent for both polymers to form a clear, non-light absorbing, colorless liquid comprising a homogenous mixture of the polymers in the solvent, such as water. The mixture, in the next step, is cast as a sheet onto a substrate to a uniform thickness, as of 0.040 inch thick. In the next step, the solvent is evaporated to leave a clear, non-light absorptive, transparent film, as of 0.010 inch thick on the substrate, The film is then peeled from the substrate to produce an electrically conductive, clear, non-light absorptive transparent film which may be utilized as the clear conductive sheet 2 of the electrographic recording web I, or which may be utilized for other applications where a transparent conductive plastic sheet is desired. In the next step, the conductive sheet 2 is coated to a thickness, as of 4 microns, with a clear charge retentive film such as of polyvinyl chloride-acetate and allowed to dry, thereby producing the electrographic recording web 1 of FIG. 2
The film forming polymeric material useful in the practice of this invention includes a wide variety of polymers which are transparent in sheets varying from thicknesses corresponding to 0.0001 inch to 1 inch. Aside from transparency, the polymer should be castable in the form of a gel, as opposed to a hard, highly crossed linked film, so as to allow ionic mobility, and its usefulness as a film should not be effected by the con tinued presence of the solvent, for example, water in the amounts required to effect ionization of the electrolyte.
Among the film forming polymers particularly preferred in the practice of this invention may be mentioned those which are polymers of hydroxyl containing monomers, esters, or acetals. Examples of such polymers include polyvinyl alcohol, agar, carboxymethylcellulose, polyvinyl acetate, polyvinyl acetate-alcohol, copolymers, polyvinyl acetal, polyvinyl formal, acrylic resins, such as polyacrylic acid, methyl cellulose, polyvinylpyrrolidone, CARBOSET 525 acrylic polymer and CARBOSET 514 acrylic polymer, the latter two being manufactured by B. F. Goodrich Chemical Company, a division of the B. F. Goodrich Company, 3135 Euclid Avenue, Cleveland 15, Ohio. It should be noted that in describing the polymers as those of named monomers, it is not implied that they are necessarily made by actual polymerization of such monomers. Thus, for example, polyvinyl alcohol may be described as a polymer of monomeric vinyl alcohol, but is invariably produced by indirect means, as vinyl alcohol is non-existent in fact.
The conductive polymer materials useful in the practice of this invention include polymers which are transparent or nearly so in thin films. The conductive polymers are capable of providing both a source of ions and the necessary waterholding capacity (hygroscopicity). Polyelectrolytes are particularly suited for this application because of their ionic nature and ability to hold water at low humidity. Particularly suitable polyelectrolytes include the quaternary ammonium polyelectrolytes. The polymers of this type include vinylbenzyl quaternary ammonium compounds and can be any water-soluble or water-dispersible homopolymer or copolymer of one or more vinylbenzyl quaternary ammonium compounds, or copolymers of a predominant amount of vinylbenzyl quaternary ammonium compound and a minor amount of a nonacidic copolymerizable compound such as acrylamide, or copolymers containing, in the polymer molecules, residues corresponding to from 95.0 to 99.99 percent by weight of one or more vinylbenzyl quaternary ammonium compounds and from 5.0 to 0.01 percent by weight of divinyl benzene. More specifically, the electroconductive substance can be a homopolymer or a copolymer of any two or more vinylbenzyl quaternary ammonium compounds having the general formula' wherein R, R and R" each represents individually a monovalent radical selected from the group consisting of CH OI-ICH CH CHOI-ICH CH OHCHOHCl-l and alkyl, aryl cycloalkyl and aralkyl hydrocarbon radicals, and R. R and R" collectively represent the radicals of the fonnula:
wherein the three valences are attached to the nitrogen atom, the R groups containing a total of not more than 12 carbon atoms in the sum of the constituent radicals, or a copolymer of at least 65 percent by weight of any one or more ofsuch vinylbenzyl quaternary ammonium compounds with not more than 35 percent by weight of acrylamide, or a copolymer containing, in the polymer molecules, residues corresponding to from 95.0 to 99.99, preferably from 99.0 to 99.99 percent by weight of any one or more of such vinylbenzyl quaternary ammonium compounds and from 5.0 to 0.01, preferably from 1.0 to 0.01, percent by weight, of divinylbenzene. Mixtures of any two or more of the homopolymers or copolymers can also be used. The polymers are of relatively high molecular weight and are characterized by a viscosity of at least 2 centipoises for a 0.5 percent by weight solution of the polymer in an aqueous 2 percent by weight solution of sodium chloride at 25 C. as determined by an Ostwald viscosimeter.
In the preferred embodiment of the invention the electroconductive polymer is a homopolymer or copolymer of one or more vinylbenzyl quaternary ammonium compounds having the aforementioned general formula wherein R represents an alkyl radical containing from one to four carbon atoms, R and R" each represents a radical of the group consisting or CH OHCl-l CH CHOHCH CH OHCHOHCH and lower alkyl radicals containing from 1 to 4 carbon atoms and Y is an anion, e.g., a sulfate, a chloride, a nitrate, or a hydroxyl ion, copolymers of at least 65 percent by weight of any two or more such vinylbenzyl quaternary ammonium compounds and not more than 35 percent by weight of acrylamide, or copolymers of from 99.0 to 99.99 percent by weight of at least one such vinylbenzyl quaternary ammonium compound and from 1.0 to 0.01 percent by weight of divinylbenzene. A particularly suitable quaternary ammonium polymer is polypiperidinium chloride having an integral heterocyclic ring as shown by the following general formula:
L H2 CH1 wherein the anion is a chloride and the polymer comprises a homopolymer of disubstituted diallyl ammonium chloride monomers where R and R are selected from the groups consisting of methyl, ethyl, and methyl, ethyl, butyl and octyl, respectively. A particular one of the aforementioned polypiperidinium chlorides is polydimethyl diallyl ammonium chloride marketed by Calgon Corporation of Pittsburgh, Pennsylvania, as conductive polymer No. 261.
Mutual solvents useful in the practice of this invention include water methanol-water mixtures.
In order to illustrate more fully the nature of the invention and the manner of practicing same, the following examples are presented.
EXAMPLES A castable composition is prepared by dissolving 15 percent by weight. polyvinyl alcohol in water. A suitable grade of polyvinyl alcohol is ELVANOL grade 70-05 available from E. l. DuPont de Nemours & Company, Inc., Organic Chemicals Department. This grade of polyvinyl alcohol is a hot-watersoluble grade and is slurried in cold water and then heated to complete solution. More particularly, add to the vessel the required amount of water at 75 F. or below and start agitation. Sift the polyvinyl alcohol into the vortex such that it is rapidly worked out and dispersed and stir this way for 10 minutes. Raise the temperatures to 194 F. or above and continue stirring at 194203 F. until the resin is completely dissolved, usually about 30-60 minutes. To the dissolved polyvinyl alcohol add polydimethyl diallyl ammonium chloride (conductive polymer 261 manufactured by Calgon Corporation) in the proportions 20 parts by weight to each parts by weight of dry polyvinyl alcohol. The conductive polymer is preferably added in a 40 percent water solution, i.e., 40 percent by weight conductive polymer in water and stirred into the polyvinyl alcohol until dispersed uniformly therein. The solution is coated on a glass plate or other suitable substrate. The coating on the glass plate substrate is obtained by spreading a pool of the solution on the substrate with a glass rod to obtain a uniform thickness for the coating of approximately 0.040 inch. The coated substrate is then put in an oven at to F. and heated until dry, typically about 30 minutes. Upon drying, the coating reduces to a thickness of approximately 0.010 inch. When dry the coated substrate is removed from the oven and allowed to cool to room temperature. Upon cooling to room temperature, the coating is stripped or peeled from the substrate to obtain the clear, transparent, conductive plastic sheet of the present invention.
In the aforecited specific example, a 25 percent solution of QX 3521 polymeric quaternary ammonia salt made by Dow Chemical Company may be substituted for polydimethyl diallyl ammonium chloride. The sheet 2 is perfectly clear, sufficiently flexible for further processing, and surprisingly resistant to finger marks, moisture or stickiness. The bulk conductivity of the sheet 2 was approximately 10 ohm centimeters when tested in ambient conditions (20 C. and 50percent relative humidity).
The amount of conductive polymer to be employed will depend to some extent upon the degree of conductivity desired. As a general rule, however, it can be said that the amount of conductive polymer should be in the range between 5 percent and 50 percent by weight of the film forming polymer.
To make an electrographic recording web, the cast sheet, after drying on the substrate, is coated with a dielectric charge retentive film as of vinyl chloride-acetate to a thickness as of 4 microns. If desired, the sheet 2 may be then stripped from the substrate or prepared in rolls or the like after the manner of making cellophane and similar films to provide a self-supporting, transparent electrically conductive sheet with a charge retentive film adhered thereto.
Since many changes could be made in the above construction and many apparently widely different embodiments of this invention could be made without departing from the scope thereof, it is intended that all matter contained in the above description or shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.
What is claimed is:
1. An electrically conductive clear transparent self-supporting plastic sheet comprising: 4
a homogenous solid molecular mixture of a clear transparent conductive polymer and a film forming clear transparent polymer;
the conductive polymer being a water-dispersible quaternary ammonium polyelectrolyte consisting of at least one member selected from the group consisting of a. homopolymers of a vinylbenzyl quaternary ammonium compound having the general formula:
wherein R, R and R" each represents individually a monovalent radical selected from the group consisting of CH OHCl-l CH CHOHCH CH OH-CHOHCH, and alkyl, aryl, cycloalkyl and aralkyl hydrocarbon radicals, and R, R and R" collectively represent the formula:
wherein the three valences are attached to the nitrogen atom, and Y is an anion, said R groups containing a total of not more than 12 carbon atoms in the substituent radicals,
b. copolymers of at least two such vinylbenzyl quaternary ammonium compounds, c. copolymers of at least 65 percent by weight of at least one of such vinylbenzyl quaternary ammonium compounds and not more than 35 percent by weight of acrylamide, and
Claims (1)
- 2. The apparatus of claim 1 wherein the film forming polymer is polyvinyl alcohol.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88373269A | 1969-12-10 | 1969-12-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3674711A true US3674711A (en) | 1972-07-04 |
Family
ID=25383220
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US883732A Expired - Lifetime US3674711A (en) | 1969-12-10 | 1969-12-10 | Electrically conductive transparent plastic material |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3674711A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3928695A (en) * | 1974-06-28 | 1975-12-23 | Dow Chemical Co | Odorless electroconductive latex composition |
| US4007148A (en) * | 1974-12-19 | 1977-02-08 | The Dow Chemical Company | Electroconductive coatings having excellent coating holdout properties |
| US4070189A (en) * | 1976-10-04 | 1978-01-24 | Eastman Kodak Company | Silver halide element with an antistatic layer |
| US4139509A (en) * | 1976-11-29 | 1979-02-13 | Kao Soap Co., Ltd. | Household starch composition prepared by emulsion-polymerizing a vinyl monomer in an aqueous solution of a polyvinyl alcohol and a nonionic starch or cellulose |
| US4149999A (en) * | 1977-10-11 | 1979-04-17 | Lockheed Aircraft Corporation | Antistatic liquid media, and method, for the controlled transport of microscopic particles |
| US4294739A (en) * | 1979-04-26 | 1981-10-13 | Eastman Kodak Company | Antistatic compositions comprising crosslinkable latex binders |
| US4454058A (en) * | 1983-02-04 | 1984-06-12 | Joseph Savit | Chemical solution for increasing the surface conductivity and/or the volume conductivity of a substrate |
| US4698391A (en) * | 1986-07-30 | 1987-10-06 | Eastman Kodak Company | Crosslinked polymers with lowered resistivity and materials and methods for their preparation |
| WO1990012489A1 (en) * | 1989-04-14 | 1990-11-01 | James River Paper Company, Inc. | Deodorization of amine contaminated quaternary ammonium salt conductive resins |
| US4981729A (en) * | 1989-05-25 | 1991-01-01 | Man-Gill Chemical Company | Electroconductive aqueous coating compositions, process, and coated substrates |
| US5370825A (en) * | 1993-03-03 | 1994-12-06 | International Business Machines Corporation | Water-soluble electrically conducting polymers, their synthesis and use |
| US5498761A (en) * | 1988-10-11 | 1996-03-12 | Wessling; Bernhard | Process for producing thin layers of conductive polymers |
| US6565731B1 (en) * | 1997-06-03 | 2003-05-20 | Shipley Company, L.L.C. | Electroplating process |
| US6830708B2 (en) | 1993-03-03 | 2004-12-14 | International Business Machines Corporation | Water-soluble electrically conducting polymers, their synthesis and use |
-
1969
- 1969-12-10 US US883732A patent/US3674711A/en not_active Expired - Lifetime
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3928695A (en) * | 1974-06-28 | 1975-12-23 | Dow Chemical Co | Odorless electroconductive latex composition |
| US4007148A (en) * | 1974-12-19 | 1977-02-08 | The Dow Chemical Company | Electroconductive coatings having excellent coating holdout properties |
| US4070189A (en) * | 1976-10-04 | 1978-01-24 | Eastman Kodak Company | Silver halide element with an antistatic layer |
| US4139509A (en) * | 1976-11-29 | 1979-02-13 | Kao Soap Co., Ltd. | Household starch composition prepared by emulsion-polymerizing a vinyl monomer in an aqueous solution of a polyvinyl alcohol and a nonionic starch or cellulose |
| US4149999A (en) * | 1977-10-11 | 1979-04-17 | Lockheed Aircraft Corporation | Antistatic liquid media, and method, for the controlled transport of microscopic particles |
| US4294739A (en) * | 1979-04-26 | 1981-10-13 | Eastman Kodak Company | Antistatic compositions comprising crosslinkable latex binders |
| US4454058A (en) * | 1983-02-04 | 1984-06-12 | Joseph Savit | Chemical solution for increasing the surface conductivity and/or the volume conductivity of a substrate |
| US4698391A (en) * | 1986-07-30 | 1987-10-06 | Eastman Kodak Company | Crosslinked polymers with lowered resistivity and materials and methods for their preparation |
| US5498761A (en) * | 1988-10-11 | 1996-03-12 | Wessling; Bernhard | Process for producing thin layers of conductive polymers |
| WO1990012489A1 (en) * | 1989-04-14 | 1990-11-01 | James River Paper Company, Inc. | Deodorization of amine contaminated quaternary ammonium salt conductive resins |
| US4981729A (en) * | 1989-05-25 | 1991-01-01 | Man-Gill Chemical Company | Electroconductive aqueous coating compositions, process, and coated substrates |
| US5370825A (en) * | 1993-03-03 | 1994-12-06 | International Business Machines Corporation | Water-soluble electrically conducting polymers, their synthesis and use |
| US5759637A (en) * | 1993-03-03 | 1998-06-02 | International Business Machines Corporation | Water-Soluable electrically conducting polymers, their synthesis and use |
| US6010645A (en) * | 1993-03-03 | 2000-01-04 | International Business Machines Corporation | Water-soluble electrically conducting polymers, their synthesis and use |
| US6103145A (en) * | 1993-03-03 | 2000-08-15 | International Business Machines Corporation | Crosslinked water-soluble electrically conducting polymers |
| US6830708B2 (en) | 1993-03-03 | 2004-12-14 | International Business Machines Corporation | Water-soluble electrically conducting polymers, their synthesis and use |
| US7166241B1 (en) | 1993-03-03 | 2007-01-23 | International Business Machines Corporation | Water-soluble electrically conducting polymers, their synthesis and use |
| US6565731B1 (en) * | 1997-06-03 | 2003-05-20 | Shipley Company, L.L.C. | Electroplating process |
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