WO1996037542A1 - Preparation of conductive polyurethanes using a conductive quasi-solution - Google Patents
Preparation of conductive polyurethanes using a conductive quasi-solution Download PDFInfo
- Publication number
- WO1996037542A1 WO1996037542A1 PCT/US1996/007247 US9607247W WO9637542A1 WO 1996037542 A1 WO1996037542 A1 WO 1996037542A1 US 9607247 W US9607247 W US 9607247W WO 9637542 A1 WO9637542 A1 WO 9637542A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- solution
- conductive
- transition metal
- polyurethane
- quasi
- Prior art date
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- 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
- Y10S521/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S521/911—Surfactant for other than polyurethane cellular product
Definitions
- Electrically conductive polymer products have been made by mixing an electrically conductive material into the polymer during formation.
- electrically conductive materials include powders such as silver, copper, nickel, carbon black, and graphite; and ionizable metal salts such as alkali metal tetraorganoborides.
- the amount of conductive powder in a conductive material can be as high as 10 - 40% by weight, which can affect the thermal and mechanical properties of the polymer. Uniform high conductivity requires uniform distribution of the conductive material throughout the polymer bulk.
- the invention features a conductive quasi-solution useful for making a homogeneously conductive single-phase polyurethane.
- the quasi-solution includes between 10% and 30% by weight of a transition metal salt, a carrier solution, a dispersing agent.
- the carrier solution includes a polyol, a polyamine, or a flame retardant.
- the carrier solution includes a flame retardant.
- the invention features a method of making a homogeneously conductive single-phase polyurethane, including preparing a conductive quasi- solution.
- the conductive quasi-solution includes a transition metal salt in dissolved and undissolved forms, a carrier solution, and a dispersing agent, wherein the transition metal salt is present in a concentration between 10 and 30% by weight and the carrier solution includes a flame retardant, a polyol, or a polyamine.
- Another step in the method is mixing the conductive quasi-solution with a diisocyanate and a polyurethane precursor selected from polyols and polyamines, whereupon the undissolved transition metal salt dissolves.
- the diisocyanate and the polyurethane precursor react to provide a homogeneously conductive single-phase polyurethane.
- the carrier solution includes polypropyl glycol, tri(chloroethyl) phosphate, tri( / 3- chloroisopropyl) phosphate, POLAMINE® 650, POLAMINE® 1000, POLAMINE® 2000, TERATHANE® 650, TERATHANE® 1000, TERATHANE® 2000, TERATHANE® 2900, TERATHANE® CL-2000, PLURACOL® Polyol 924, PLURACOL® Polyol 538, PLURACOL® Polyol 774, or butanediol XB, or a combination thereof.
- the dispersing agent is RC® Dispersant, DC®-190, DC®-193, or DABCOTM DC 5418, or a combination thereof.
- the invention features a method of making a homogeneously conductive single-phase polyurethane, including the steps of preparing a conductive quasi-solution and mixing an amount of the conductive quasi-solution with a diisocyanate and a polyurethane precursor to form a homogeneously conductive single-phase polyurethane (i.e., a solid solution).
- the polyurethane precursor is selected from polyols and polyamines. Mixing is accomplished according to either a conventional reaction injection molding process, or a conventional thermoplastic polyurethane production process.
- the conductive thermoset and thermoplastic polyurethanes have many applications. Examples include coated integrated circuit boards, car body parts, especially those which are to have a painted (baked) surface, such as bumpers and side panels; and durable carrying cases or other accessories in the electronics (e.g., computer) field for which dissipation of static charge is desirable.
- the transition metal salt provides conductive properties to the polyurethane.
- homogeneously conductive means that conductivity is essentially uniform across the surface and throughout the volume of the bulk polyurethane, due to the uniform distribution of fully-dissolved transition metal salts throughout the polymer.
- the polymer is thus a single- phase solid solution of polymer and dissolved transition metal salts, with an absence of transition metal salt particles.
- the methods of the invention produce single- phase conductive polyurethanes, which are therefore homogeneously conductive.
- the invention generally features the use of a conductive quasi-solution to make a homogeneously conductive, single phase polyurethane.
- the conductive quasi-solution is a dispersion including a transition metal cation, a dispersing agent, and a carrier.
- a conductive quasi-solution has both dissolved and undissolved transition metal salt, the maximum diameter of undissolved particles being 0.5 ⁇ m, and preferably 0.1 ⁇ m.
- the invention resides, in part, in the discovery that a quasi-solution of transition metal salts will produce a conductive single-phase polyurethane product.
- This product whether formed by reaction injection molding or conventional thermoplastic polyurethane production, is a solid solution, rather than a dispersion of undissolved transition metal salts in the polymer.
- the undissolved transition metal particles dissolve into the forming polymer.
- a copper (II) chloride quasi-solution a brown dispersion with undissolved copper salt particles
- the urethane precursor(s) results in a clear, dark green solution without any precipitated or undissolved copper salt particles.
- transition metal cations form d- orbital complexes with nucleophilic oxygen (i.e., carbonyl) and nitrogen atoms. Such complexes form bridged networks between different polyurethane polymer molecules, which improves uniformity and conductivity.
- a transition metal salt is capable of carrying or conducting an electric charge.
- a transition metal salt includes a transition metal cation and one or more counter-anions to form a neutral salt.
- Each counter-anion may be any anion that does not interfere with the homogeneity or semi- conductivity of the final polymer product.
- transition metal cations include Cu (II) , Co (II) , Zn (II) , Ni (II) , Fe (II) , and Fe (III) .
- Fe (III) and Cu (II) are preferred.
- Examples of counter-anions include fluoride, chloride, bromide, iodide, cyanide, thiocyanate, acetate, lactate, phosphate, and tartrate.
- transition metal salts include CuCl 2 , CuBr 2 , Cu(CH 3 COO) 2 , Cu(SCN) 2 , FeBr 3 , Fe(SCN) 3 , FeCl 2 , CuCl 2 , and Fe(CH 3 COO) 3 .
- Transition metal salts are available commercially from, e.g., Aldrich Chemical Co. (Milwaukee, I) .
- the conductive quasi-solution preferably has a transition metal salt concentration (w/w in carrier and dispersing agent) of between 10 and 30%, and more preferably between 15 and 25%.
- a transition metal salt concentration (w/w in carrier and dispersing agent) of between 10 and 30%, and more preferably between 15 and 25%.
- the concentration (w/w) of transition metal salts in the final product is between 0.02 and 1.0%, and is preferably between 0.04 and 0.2% (see, e.g., Example 12).
- the mole percent of transition metal salts in the final product is between 1.52 x 10 ⁇ 4 and 7.4 x 10 ⁇ 3 mole percent, and preferably between 3.0 x 10 ⁇ 4 and 1.5 x 10 ⁇ 3 mole percent.
- more than one transition metal salts are used; as a result, more than one transition metal cation or more than one counter- anion is present in the conductive quasi-solution.
- a carrier solution is one or more organic solvents, the combination solution being stable at high temperature.
- a temperature- stable non-aqueous liquid is characterized by a high boiling point and a low vapor pressure.
- a high boiling point is a boiling point of at least 350 °F, and preferably at least 500 °F.
- a low vapor pressure is a vapor pressure of no more than 50 mm Hg at 110 °C.
- a low vapor pressure is also characterized by the visual absence of white smoke at 300 °F.
- carrier solutions include flame retardants such as tri(haloalkyl)phosphates, and preferably tri(chloroethyl)phosphate ("FYROL® CEF,” Akzo Chemical Corp., Chicago, IL) and tri(, ⁇ -chloroisopropyl)phosphate ("PCF”); polyamines such as POLAMINE®-650, POLAMINE®- 1000, and POLAMINE®-2000 (Air Products, Allentown, PA); and polyols such as polypropyleneglycol (“PPG”) , TERATHANE® 650, TERATHANE® 1000, TERATHANE® 2000,
- flame retardants such as tri(haloalkyl)phosphates, and preferably tri(chloroethyl)phosphate (“FYROL® CEF,” Akzo Chemical Corp., Chicago, IL) and tri(, ⁇ -chloroisopropyl)phosphate (“PCF”
- polyamines such as POLAMINE®-650, POL
- TERATHANE® is a polytetramethylene ether glycol (PTMEG) with different molecular weights as indicated.
- PLURACOL® polyols are polypropylene glycol-type compounds.
- PLURACOL® Polyol 774 is a 3500 molecular weight polyoxypropylene-polyoxyethylene containing polyol
- PLURACOL® Polyol 924 is a 3300 molecular weight polyoxypropylene-polyoxyethylene containing polyol.
- PLURACOL® Polyol 380 and PLURACOL® Polyol 945 are high molecular weight polyols with a hydroxyl number (Mg, KOH/gm) of 25, and 35, respectively.
- PLURACOL® Polyol 816 and PLURACOL® Polyol 538 are high molecular weight triols each having a hydroxyl number of 35.
- POLAMINE®-650, -1000, and -2000 are oligomeric dia ines (polytetramethylene-oxide-di-p-aminobenzoate) with average molecular weight ranges of 710-950, 1238, and 1820-2486, respectively.
- more than one solvent is present in the conductive quasi-solution, such as the following carrier combinations: a polyol and a polyamine; two polyols; two polyamines; a flame retardant and a polyol; a flame retardant and a polyamine; or a flame retardant, a polyol, and a polyamine.
- Dispersing agent a polyol and a polyamine; two polyols; two polyamines; a flame retardant and a polyol; a flame retardant and a polyamine; or a flame retardant, a polyol, and a polyamine.
- a dispersing agent is a non-ionic surfactant which acts to stabilize the metal salt in the conductive quasi-solution before use in a reaction injection molding process. After mixing, the dispersing agent also improves solubility of the transition metal salt, improves uniform mixing, and thus improves the conductive homogeneity of the final product. Stabilization of the conductive quasi-solution includes increasing the solubility of the transition metal salt without increasing the percent of carrier.
- dispersing agents include DC 190 and DC 193 (Dow Corning Corp., Midland, MI), DABCOTM DC 5418 (Air Products Co.) and RC® Dispersant WM (Rhein Chemie Corp. , Trenton, NJ) .
- Dispersant WM is ethoxylated oxydiphenyl, a non-ionic emulsifier.
- DC®-190 is dimethyl, methyl(polyethylene oxide polypropylene oxide acetate-capped) siloxane copolymer (63%) and DC®-193 is dimethyl, methyl(polyethylene oxide) siloxane copolymer (88%).
- DABCO® DC 5418 is a silicone surfactant or dispersion agent; its composition is a trade secret of Air Products and Chemicals, Inc., Allentown, PA. Dispersing agents are present in the quasi-solution at a concentration between 0.5 and 5%, and preferably 1 and 3% (w/w).
- the conductive quasi-solution of the invention may be used in either a two stream process (streams A and B) or a three stream process (streams A, B, and C) to produce a molded homogeneously conductive polyurethane form.
- the mixing step may be part of either a conventional reaction injection molding process or a conventional production method of making thermoplastic polyurethane.
- a diisocyanate can be in prepolymer form (i.e., partially cured with a polyol or polyamine) or pure form, such as methylene diisocyanate (MDI) or toluene diisocyanate (TDI) (BASF Corp.).
- stream A includes a diisocyanate in either a prepolymer form such as the commercially available BAYFLEX® 110-25A (Bayer Corp, Pittsburgh, PA) or pure form, such as ISOCYANATE® 76 and ISOCYANATE® 227 from BASF.
- Stream B includes a conductive quasi-solution at a concentration between 0.2 to 2.0% by weight, and a polyurethane precursor such as a polyol or a polyamine in a solvent such as BAYFLEX® 110- 35B, IMR (Bayer Corp.).
- Stream B also may include a catalyst such as an amine catalyst, a tin catalyst, or a bismuth catalyst, in a concentration between 0.01 and
- DABCO® T-12 catalyst is dibutyltin dilaurate.
- DABCO® T-9 catalyst is a proprietary composition containing stannous octoate;
- DABCO® 33-LV catalyst is a proprietary composition containing diazabicyclo- ⁇ 2,2,2>octane (33%) and 1,4- dipropylene glycol (67%) .
- the composition of FOMREZ UL- 32, an alkyltin mercaptide catalyst, is a trade secret.
- stream A includes a diisocyanate as above.
- Stream B includes a polyurethane precursor such as a polyol or a polyamine.
- the total concentration of polyol and polyamine is at least 95%, the remainder being additives such as lubricants (e.g., internal mold release materials), catalysts, pigments, mineral additives (e.g., glass fibers, iron oxide, carbon black, or graphite) .
- Stream C includes the conductive quasi-solution. Stream C may also include additives such as pigment.
- the streams are mixed at a specified flow rate ratio, temperature, and pressure at the mixing head and rapidly injected into the mold, e.g., within 1 or 2 seconds.
- a person of skill in the art will easily be able to determine the specific ratios, temperatures, and pressures to be used. See, e.g., Example 12.
- the conductive quasi-solution of the invention has a very short pot life (e.g., less than 5 seconds) .
- a polyurethane precursor such as a polyol or a polyamine or a combination thereof
- the previously-undissolved transition metal salt particles in the conductive quasi-solution completely dissolve.
- a single-phase solid solution polyurethane is formed.
- the concentration (w/w) of the quasi-solution in the final product is between 0.1 and 5 % and preferably between 0.2 and 1.0%.
- FYROL CEF tri-( / 3-chloroethyl)phosphate (2475 g, Akzo Corp, Chicago, IL) was added to a four liter flask.
- RC Dispersant WM 125 g, Rhein Chemie Corp., Trenton, NJ
- 650 g of CuCl 2 Aldrich Chemical, Milwaukee, WI
- a uniform. conductive quasi-solution was formed, having a transition metal salt concentration of 20% by weight.
- Example 2 Procedure according to Example 1, except 650 g of FeCl 3 was added, instead of 650 g CuCl 2 .
- Example 3 Procedure according to Example 1, except 325 g of FeCl 3 and 325 g CuCl 2 were added, instead of 650 g CuCl 2 .
- Example 4 Procedure according to Example 1, except tri(9- chloroisopropyl)phosphate was added instead of (tri-( / 3- chloroethy1)phosphate.
- Example 5 Procedure according to Example 1, except a polyol solution was added instead of FYROL® CEF, for use in RIM.
- Example 6 Procedure according to Example 1, except a polyamine solution was added instead of FYROL® CEF, for use in RIM.
- Example 8 Procedure according to Example 1, except a solution including both polyamine and polyol was added instead of FYROL® CEF, for use in RIM.
- Example 8 Procedure according to Example 1, except a thermo ⁇ plastic polyol solution was added instead of FYROL® CEF, for use in making a thermoplastic polyurethane.
- thermo ⁇ plastic polyamine solution was added instead of FYROL® CEF, for use in making a thermoplastic polyurethane.
- Example 10 Procedure according to Example 1, except a solution including both polyamine and polyol was added instead of FYROL® CEF, for use in making a thermoplastic polyurethane.
- Example 11 Procedure according to Example 1, except one or more transition metal salts selected from CuBr 2 , Cu(CH 3 COO) 2 , Cu(SCN) 2 , FeBr 3 , Fe(CH 3 COO) 3 , Fe(SCN) 3 FeCl 3 , and CuCl 2 . v
- BAYFLEX® 110-35A, part A, and BAYFLEX® 110-35B,IMR or BAYFLEX® 110-35B, part B were obtained from Bayer Corp., Pittsburgh, PA.
- the conductive quasi-solution of Example 1 was premixed with part B to form a conductive polyurethane precursor solution.
- An Admiral 2640-2 high pressure, high temperature RIM machine was used to form a plaque having a transition metal salt concentration in the final product of 0.25%, 0.50%, and 0.75%.
- the process parameters were as follows: 2.0 lb/sec injection rate, 1.20 sec injection time, 45 sec cure time.
- Part A diisocyanate
- Part B polyol or polyamine
- the plaque size was 22" by 28".
- a ChemTrend® 2006 mold release, zinc stearate aqueous solution wash soap was used. The plaque was cured at 250 °F for 1 hour and washed with the zinc stearate soap. Electrical paint was applied at 85 kV with a gun speed of 30 ips. A superior, uniform paint coat was achieved (see Table I) .
- Example 13 Procedure according to Example 12, except the following was used: part A (BAYFLEX® 110-25A) ; part B (BAYFLEX® 110-25B premixed with a conductive quasi- solution having a 10% by weight CuCl 2 transition metal salt concentration). The mixing time was 1.2 seconds at 150 °F; the material was postcured for 1 hour at 260-270 °F, and then electrically painted to yield a uniform paint coat with an excellent appearance and good fastness (see Table II) .
- Example 14 Thermoplastic polyurethane (TPU) is made by mixing a conductive quasi-solution (0.1 to 10%) into a polyol or polyamine to form a conductive precursor solution. The precursor solution is reacted with pure diisocyanate at a temperature between 100 and 240 °F to form thermoplastic polyurethane. The polyurethane material is completely cured at 200 °F for 12 hours and cooled to room temperature. After cooling, the material is extruded and formed into pellets for packing. The urethane product is semiconductive, and useful for static charge dissipation with a volume resistivity between about E8 and E10 ohm- cm.
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96920302A EP0828782A4 (en) | 1995-05-25 | 1996-05-20 | Preparation of conductive polyurethanes using a conductive quasi-solution |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/448,726 | 1995-05-25 | ||
US08/448,726 US5639847A (en) | 1995-05-25 | 1995-05-25 | Preparation of conductive polyurethanes using a conductive quasi-solution |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996037542A1 true WO1996037542A1 (en) | 1996-11-28 |
Family
ID=23781445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/007247 WO1996037542A1 (en) | 1995-05-25 | 1996-05-20 | Preparation of conductive polyurethanes using a conductive quasi-solution |
Country Status (4)
Country | Link |
---|---|
US (2) | US5639847A (en) |
EP (1) | EP0828782A4 (en) |
CA (1) | CA2218994A1 (en) |
WO (1) | WO1996037542A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998011562A1 (en) * | 1996-09-12 | 1998-03-19 | Uniroyal Chemical Company, Inc. | Electrically conductive polyether polyurethanes |
US6111051A (en) * | 1998-08-07 | 2000-08-29 | Mearthane Products Corporation | Preparation of conductive polyurethanes using a conductive quasi-solution |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3000944B2 (en) * | 1996-06-24 | 2000-01-17 | 富士ゼロックス株式会社 | Semiconductive member and semiconductive cleaning and static elimination blade |
US6093451A (en) | 1998-01-30 | 2000-07-25 | Pilkington Aerospace Inc. | Coated transparencies and transparent laminates incorporating a transparent polyurethane composition |
US6103459A (en) * | 1999-03-09 | 2000-08-15 | Midwest Research Institute | Compounds for use as chemical vapor deposition precursors, thermochromic materials light-emitting diodes, and molecular charge-transfer salts and methods of making these compounds |
KR100329213B1 (en) * | 1999-07-20 | 2002-03-22 | 전종한 | Composition for Preparing Conductive Polyurethanes |
AU1467501A (en) | 1999-11-03 | 2001-05-14 | Nexicor Llc | Hand held induction tool |
US20020190426A1 (en) * | 2001-02-09 | 2002-12-19 | Seidner Nathan M. | Static dissipative mold release agent and use in casting and molding processes |
AU2003224982A1 (en) * | 2002-04-12 | 2003-10-27 | Fritz H. Obermeyer | Multi-axis joystick and transducer means therefore |
US20060020100A1 (en) * | 2004-07-20 | 2006-01-26 | Shirley Lee | Conductive agents for polyurethane |
US7173805B2 (en) * | 2004-07-20 | 2007-02-06 | Hewlett-Packard Development Company, L.P. | Polymer material |
US20080073622A1 (en) * | 2006-09-22 | 2008-03-27 | Inolex Investment Corporation | Conductive polyurethane foam and methods for making same |
EP2385960B1 (en) | 2009-01-12 | 2020-03-11 | University Of Massachusetts Lowell | Polyisobutylene-based polyurethanes |
AU2010284137B2 (en) | 2009-08-21 | 2014-11-27 | Cardiac Pacemakers, Inc. | Crosslinkable polyisobutylene-based polymers and medical devices containing the same |
US8374704B2 (en) | 2009-09-02 | 2013-02-12 | Cardiac Pacemakers, Inc. | Polyisobutylene urethane, urea and urethane/urea copolymers and medical leads containing the same |
US8644952B2 (en) | 2009-09-02 | 2014-02-04 | Cardiac Pacemakers, Inc. | Medical devices including polyisobutylene based polymers and derivatives thereof |
US8660663B2 (en) | 2010-12-20 | 2014-02-25 | Cardiac Pacemakers, Inc. | Lead having a conductive polymer conductor |
US9926399B2 (en) | 2012-11-21 | 2018-03-27 | University Of Massachusetts | High strength polyisobutylene polyurethanes |
WO2018165273A1 (en) | 2017-03-07 | 2018-09-13 | Cardiac Pacemakers, Inc. | Hydroboration/oxidation of allyl-terminated polyisobutylene |
CN110997746B (en) | 2017-08-17 | 2021-12-28 | 心脏起搏器股份公司 | Photocrosslinked polymers for enhanced durability |
US11118086B2 (en) | 2017-11-22 | 2021-09-14 | GKN Aerospace Transparency Systems, Inc. | Durable, electrically conductive transparent polyurethane compositions and methods of applying same |
EP3740253B1 (en) | 2018-01-17 | 2023-08-16 | Cardiac Pacemakers, Inc. | End-capped polyisobutylene polyurethane |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0566418A2 (en) * | 1992-04-16 | 1993-10-20 | Mearthane Products Corp. | Electrically conductive and semi-conductive polymers |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3725308A (en) * | 1968-12-10 | 1973-04-03 | M Ostolski | Electrically conductive mass |
JPS4997845A (en) * | 1972-12-28 | 1974-09-17 | ||
JPS4997846A (en) * | 1972-12-29 | 1974-09-17 | ||
JPS4997847A (en) * | 1972-12-29 | 1974-09-17 | ||
US4231901A (en) * | 1978-06-23 | 1980-11-04 | Charleswater Products, Inc. | Electrically conductive foam and method of preparation and use |
DE2845674A1 (en) * | 1978-10-20 | 1980-05-08 | Kabel Metallwerke Ghh | Siloxane crosslinkable thermoplastics conductive polymer mixt. - contains highly structured non-hygroscopic carbon black as conductive filler |
JPS5730319A (en) * | 1980-07-31 | 1982-02-18 | Fujitsu Ltd | Automatic manufacturing equipment of integrated circuit device |
US4393719A (en) * | 1981-07-20 | 1983-07-19 | United Technologies Corporation | Ionization flowmeter |
US4547313A (en) * | 1983-04-18 | 1985-10-15 | Phillips Petroleum Company | Conductive polymer composition |
JPS6025159A (en) * | 1983-07-21 | 1985-02-07 | Matsushita Electric Ind Co Ltd | Manufacture of nonaqueous electrolyte battery |
DE3335513A1 (en) * | 1983-09-30 | 1985-04-18 | Bayer Ag, 5090 Leverkusen | ORGANIC POLYMERS STABILIZED AGAINST HCN SPLITTERING, CONTAINING TCNQ COMPLEXES |
JPS60168632A (en) * | 1984-02-13 | 1985-09-02 | Japan Styrene Paper Co Ltd | Expanded molding of bridged polypropylene resin |
JPS60189229A (en) * | 1984-03-09 | 1985-09-26 | Toshiba Chem Corp | Semiconductor device |
US4617325A (en) * | 1984-08-27 | 1986-10-14 | The Dow Chemical Company | Organic polymers containing antistatic agents comprising the polymer having dispersed therein a non-volatile ionizable metal salt and a phosphate ester |
US4581158A (en) * | 1984-09-26 | 1986-04-08 | W. R. Grace & Co. | Conductive thermosetting compositions and process for using same |
JPS61264053A (en) * | 1985-01-07 | 1986-11-21 | Mitsui Toatsu Chem Inc | Production of electrically-conductive resin composite material |
US4652399A (en) * | 1985-03-11 | 1987-03-24 | Armstrong World Industries, Inc. | Novel polyacrylic esters bearing pendant macrocyclic ethers and electrically conducting compositions comprised thereof |
JPS62256990A (en) * | 1986-04-30 | 1987-11-09 | Nippon Steel Corp | Roll for stripe plating |
US4654279A (en) * | 1986-07-10 | 1987-03-31 | The United States Of America As Represented By The Secretary Of The Navy | Interpenetrating-network polymeric electrolytes |
JPS6348561A (en) * | 1986-08-18 | 1988-03-01 | Seiko Epson Corp | Electrophotographic sensitive body |
DE3629606A1 (en) * | 1986-08-30 | 1988-03-03 | Agfa Gevaert Ag | METHOD FOR PRODUCING MAGNETIC RECORDING CARRIERS |
US4886626A (en) * | 1987-05-19 | 1989-12-12 | Crest-Foam Corporation | Conductive polyurethane foam compositions containing tetralyanoethylene and method |
JPH01109663A (en) * | 1987-10-23 | 1989-04-26 | Mitsubishi Plastics Ind Ltd | Electrode plate for cell |
US5077330A (en) * | 1988-08-29 | 1991-12-31 | Armstrong World Industries, Inc. | Conductive polyurethane-urea/polyethylene oxide |
DE59203441D1 (en) * | 1991-07-02 | 1995-10-05 | Ciba Geigy Ag | Radical cation salts of tetrathiotetracene and copper chloride, their preparation and their use. |
ATE123515T1 (en) * | 1991-07-02 | 1995-06-15 | Ciba Geigy Ag | METHOD FOR PRODUCING ELECTRICALLY CONDUCTIVE LAYERS. |
-
1995
- 1995-05-25 US US08/448,726 patent/US5639847A/en not_active Expired - Lifetime
-
1996
- 1996-05-20 EP EP96920302A patent/EP0828782A4/en not_active Withdrawn
- 1996-05-20 CA CA002218994A patent/CA2218994A1/en not_active Abandoned
- 1996-05-20 WO PCT/US1996/007247 patent/WO1996037542A1/en not_active Application Discontinuation
-
1997
- 1997-05-27 US US08/863,212 patent/US5898057A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0566418A2 (en) * | 1992-04-16 | 1993-10-20 | Mearthane Products Corp. | Electrically conductive and semi-conductive polymers |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6184331B1 (en) | 1995-05-25 | 2001-02-06 | Mearthane Products Corporation | Preparation of conductive polyurethanes using a conductive quasi-solution |
US6417315B2 (en) | 1995-05-25 | 2002-07-09 | Mearthane Products Corporation | Preparation of conductive polyurethanes using a conductive quasi-solution |
WO1998011562A1 (en) * | 1996-09-12 | 1998-03-19 | Uniroyal Chemical Company, Inc. | Electrically conductive polyether polyurethanes |
US6111051A (en) * | 1998-08-07 | 2000-08-29 | Mearthane Products Corporation | Preparation of conductive polyurethanes using a conductive quasi-solution |
Also Published As
Publication number | Publication date |
---|---|
EP0828782A1 (en) | 1998-03-18 |
CA2218994A1 (en) | 1996-11-28 |
EP0828782A4 (en) | 2001-03-21 |
US5898057A (en) | 1999-04-27 |
US5639847A (en) | 1997-06-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5639847A (en) | Preparation of conductive polyurethanes using a conductive quasi-solution | |
US6111051A (en) | Preparation of conductive polyurethanes using a conductive quasi-solution | |
CN101605842B (en) | Conductive polymer foams, method of manufacture, and uses thereof | |
US4621106A (en) | Polyester polyurethane foams having antistatic properties | |
US20060121287A1 (en) | Polymer materials with electrostatic dissipative properties | |
JPH02209962A (en) | Electrically conductive polyurethane form foamable at proper place | |
JPH0138804B2 (en) | ||
US6361484B1 (en) | Electrically conductive and semi-conductive polymers | |
US4886626A (en) | Conductive polyurethane foam compositions containing tetralyanoethylene and method | |
NZ235530A (en) | Fire-retardant compositions containing a solid fire-retardant and polymer particles dispersed in a liquid poly isocyanate | |
US20040259966A1 (en) | Static dissipative polyurethane foams | |
JP2855335B2 (en) | Method for producing conductive polyurethane foam | |
US4914150A (en) | Process for preparing anti-static polyisocyanate-based polymers via incorporating a polyalkylene carbonate-salt mixture | |
JP2002146178A (en) | Additive for producing antistatic polyurethane, antistatic polyurethane and method for producing antistatic polyurethane | |
JPH05500826A (en) | Conductive polymers and methods of making such polymers | |
JPH0733977A (en) | Conductive polyurethane elastomer | |
JP3356188B2 (en) | Conductive roller for image forming device | |
CN111718464A (en) | High-density conductive polyurethane foam, preparation method thereof and adhesive tape | |
JP4684395B2 (en) | Antistatic polyurethane resin composition | |
JPH0762276A (en) | Electrically conductive polymer composite and its production | |
JPH037716A (en) | Flame-retarding polyurethane composition | |
USH1928H (en) | High viscosity, solvent resistant, thermoset polyetherpolyurethane and A process for making the same | |
JPH03177414A (en) | Non-chargeable polyurethane foam for various kinds of roller material and its production | |
JP2836848B2 (en) | Thermoplastic elastomer composition and molded article thereof | |
JPH03273019A (en) | Castable flame-retarding urethane composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): CA |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
ENP | Entry into the national phase |
Ref document number: 2218994 Country of ref document: CA Ref country code: CA Ref document number: 2218994 Kind code of ref document: A Format of ref document f/p: F |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1996920302 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 1996920302 Country of ref document: EP |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 1996920302 Country of ref document: EP |