EP0074281A1 - Heating Diesel fuel - Google Patents
Heating Diesel fuel Download PDFInfo
- Publication number
- EP0074281A1 EP0074281A1 EP82304744A EP82304744A EP0074281A1 EP 0074281 A1 EP0074281 A1 EP 0074281A1 EP 82304744 A EP82304744 A EP 82304744A EP 82304744 A EP82304744 A EP 82304744A EP 0074281 A1 EP0074281 A1 EP 0074281A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fuel
- heater
- composition
- feedthrough
- conductive polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000010438 heat treatment Methods 0.000 title claims abstract description 12
- 239000002283 diesel fuel Substances 0.000 title claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 45
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims abstract description 21
- 229920001940 conductive polymer Polymers 0.000 claims abstract description 19
- 239000002033 PVDF binder Substances 0.000 claims abstract description 18
- 239000000446 fuel Substances 0.000 claims description 38
- 239000006229 carbon black Substances 0.000 claims description 10
- 239000011231 conductive filler Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000002828 fuel tank Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 238000009413 insulation Methods 0.000 claims description 2
- 239000012530 fluid Substances 0.000 abstract description 3
- 229920000642 polymer Polymers 0.000 description 9
- 239000007788 liquid Substances 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 6
- 235000010446 mineral oil Nutrition 0.000 description 6
- 239000002245 particle Substances 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920010177 Kynar® 460 Polymers 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052806 inorganic carbonate Inorganic materials 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 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
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/24—Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01C—RESISTORS
- H01C7/00—Non-adjustable resistors formed as one or more layers or coatings; Non-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material
- H01C7/02—Non-adjustable resistors formed as one or more layers or coatings; Non-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material having positive temperature coefficient
- H01C7/027—Non-adjustable resistors formed as one or more layers or coatings; Non-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material having positive temperature coefficient consisting of conducting or semi-conducting material dispersed in a non-conductive organic material
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
- H05B3/12—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material
- H05B3/14—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material the material being non-metallic
- H05B3/146—Conductive polymers, e.g. polyethylene, thermoplastics
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B3/00—Engines characterised by air compression and subsequent fuel addition
- F02B3/06—Engines characterised by air compression and subsequent fuel addition with compression ignition
Definitions
- This invention relates to conductive polymer compositions and devices comprising them.
- Electrical devices containing conductive polymers generally (though not invariably) comprise an outer jacket, usually of insulating material, to protect the conductive polymer from damage by the surrounding environment.
- an outer jacket usually of insulating material
- the jacket is permeable to harmful species in the environment, or if the conditions of use are such that the jacket may become damaged, it is necessary or desirable to select a conductive polymer which is not damaged (or which deteriorates at an acceptably low rate) when exposed to the surrounding environment.
- Exposure of conductive polymers to organic fluids generally results in an increase in resistivity; exposure to air, especially at elevated temperatures between room temperature and 35°C below the melting point generally results in a decrease in resistivity both at the elevated temperature and at room temperature (a phenomenon known in the art as "resistance relaxation").
- conductive polymer compositions which are based on polyvinylidene fluoride exhibit substantially improved stability if the polyvinylidene fluoride has a very regular structure which can be characterized by a low head-to-head content in the repeating units.
- Polyvinylidene fluoride is made up of repeating units of formula -CH 2 CF 2 -, which can be arranged head-to-tail ( i .e. - CH 2 CF 2 -CH 2 CF 2 -) or head-to-head (i.e.
- the present invention provides a conductive polymer composition which comprises (a) polyvinylidene fluoride having a head-to-head content of less than 5.0%, preferably less than 4.5%, particularly less than 4.0%, and (b) a particulate conductive filler, especially carbon black, dispersed in the polyvinylidene fluoride.
- the composition preferably exhibits PTC behavior.
- the invention provides an electrical device which comprises a conductive polymer element composed of a conductive polymer composition as defined above and at least one electrode in electrical contact with said element, for example, at least two electrodes which can be connected to a source of electrical power and which when so connected cause current to flow through the conductive polymer element.
- Preferred devices are self-limiting heaters, e.g. flexible strip heaters, in which the conductive polymer composition exhibits PTC behavior. Such heaters are particularly useful for heating liquids in which the heater is immersed, especially diesel fuel (see U.K. applications Nos. 8216999 and 8216997.
- the invention provides a method of heating a liquid, particularly an organic liquid, especially diesel fuel, which comprises passing current through a self-limiting heater as defined above which is immersed in the liquid.
- the invention provides a fuel feedthrough and heating assembly which can be positioned and connected between a fuel filter and a fuel tank of a fuel supply system to provide means for heating fuel which is being pumped through a fuel line from the fuel tank to the fuel filter, said feedthrough and heating assembly comprising
- Polyvinylidene fluorides suitable for use in this invention are commercially available.
- the head-to-head content of a polyvinylidene fluoride can be measured by those skilled in the art. We have found that the measured head-to-head contents of different samples of a polymer sold under & particular trade name can differ substantially.
- the presently available polyvinylidene fluorides made by suspension polymerization (rather than emulsion polymerization) have lower head-to-head contents.
- the number average molecular weight of the polymer is generally at least 5,000, eg. 7,000 to 15,000.
- the polyvinylidene fluoride is preferably a homopolymer of vinylidene fluoride, but the presence of small quantities of comonomers, (preferably less than 15%, particularly less than 5% by weight), eg. tetrafluoroethylene, hexafluoropropylene and ethylene, is not excluded.
- the polyvinylidene fluoride is preferably the sole crystalline polymer in the composition, but other crystalline polymers, eg. other crystalline fluoropolymers, may also be present.
- the composition may contain relatively small amounts (preferably less than 35%, especially less than 20%, particularly less than 10%, by volume)-of one or more elastomeric polymers, particularly solvent-resistant fluorine-containing elastomers and acrylic elastomers, which are usually added primarily to improve the flexibility and elongation of the composition.
- the particulate conductive filler preferably comprises carbon black, and often consists essentially of carbon black. Choice of the carbon black will influence the resistivity/temperature characteristics of the composition. Compositions exhibiting PTC behavior are preferred for many devices of the invention, especially self-limiting heaters, and for these a carbon black having a ratio of surface area (m 2 /g) to particle size (mu) of 0.03 to 6.0 is preferred. For other uses, compositions exhibiting ZTC or NTC behavior may be preferred. The amount of conductive filler used will depend upon the desired resistivity of the composition.
- a PTC composition whose resistivity at 25°C is less than 200 ohm.cm eg. about 10 to about 100 ohm.cm.
- the amount of carbon black may for example be 16 to 25% by weight.
- compositions may also comprise other conventional additives, such as non-conductive fillers (including flame retardants), antioxidants and crosslinking agents (or residues thereof if the composition has been cross-linked).
- non-conductive fillers including flame retardants
- antioxidants include antioxidants and crosslinking agents (or residues thereof if the composition has been cross-linked).
- compositions of the invention are preferably cross-linked (particularly by irradiation), since this has been found to enhance their resistance to organic solvents.
- compositions of the invention can be carried out in conventional fashion. Often it will be convenient to melt-extrude the composition directly into a water bath (which may be heated), and using this technique subsequent annealing is often not required.
- composition A in-Table 1 The ingredients listed for Composition A in-Table 1 below were mixed in a Banbury mixer. The mixture was dumped, placed on a steam-heated mill and extruded into a water bath through a 3.5 inch (8.9 cm) extruder fitted with a pelletizing die. The extrudate was chopped into pellets which were dried for 16 hours at 80°C.
- composition B The ingredients listed for Composition B in Table 1 were mixed and'pelletized in the same way as for Composition A.
- the composition of the resulting Final Blend is shown in Table 1.
- Table 1 Using a 1.5 inch (3.8 cm) diameter extruder fitted with a crosshead die having an orifice 0.4 inch (1.0 cm) x 0.1 inch (0.3 cm), the blend was melt-extruded over a pair of pre-heated 14 AWG (1.85 mm diameter) 19/27 nickel-coated copper wires with a center-to-center separation of 0.25 inch (0.64 cm).m.
- the extrudate was passed immediately through a bath of water at room temperature, air-dried, and then irradiated to a dosage of 10 Mrad.
- the conductive polymer had a resistivity of about 50 ohm.cm at 25°C.
- Kynar 460 is polyvinylidene fluoride available from Pennwalt and having a head-to-head content of about 5.5%.
- Furnex N765 is a carbon black available from Columbia Chemical having a particle size of about 60 millimicrons, a surface area of about 32 m2/g and a DBP value of about 112 cm 3 /100 g.
- Viton AHV is a copolymer of hexafluoropropylene and polyvinylidene fluoride manufactured by du Pont.
- Omya-BSH is calcium carbonate available from Omya Inc.
- T AIC is triallyl isocyanurate, a radiation cross-linking agent.
- K ynar 450 is polyvinylidene fluoride available from Pennwalt and having a head-to-head content in the range 5.5 to 6.3.
- Solef-1010 is a polyvinylidene fluoride available from Solvay et cie of Belgium, and having a head-to head content of 4.1%.
- KF1000 and KF1100 are polyvinylidene fluorides available from Kureha Chemical Industry Co. of Japan, and having a head-to-head content of 3.5 to 3.8%.
- Statex G is a carbon black available from Cities Services Co., Columbian Division having a particle size of about 60 millimicrons, a surface area of about 32 m 2 /g and a DB P value of about 90 cm 3 /100 g.
- Dyflor 2000 M is a polyvinylidene fluoride available from Kay-Fries, Inc., member of Dynamit Nobel Chemikalien of Federal Republic of Germany and having a head-to-head content of about 4.4-4.9.
- Vulcan XC-72 is a carbon black available from Cabot Co., having a particle size of about 30 millimicrons, a surface area of about 224 m2/g and a DBP value of about 178 c m 3 / 1 00 g.
- Example 1 and 4 The extrudates obtained in Examples 1 and 4 were compared by the following tests. Samples 2 inch (5.1 cm) long were cut from the extrudates. The samples were immersed in various solvents at 25°C and the resistance of the samples was measured at intervals. The solvents used, and their solubility parameters, were The results for Examples 1 and 4 are shown in Figures 1 and 2 respectively of the accompanying drawings, where the ratio of the resistance at a given time (R f ) to the initial resistance (R i ) is plotted against time. The greater stability of the composition of the invention (Example 4, shown in Figure 2) is apparent.
- the extrudates obtained in Examples 1 to 6 were compared in the following way. Samples 2 inch (5.1 cm) long were cut from the extrudates and were immersed in various test liquids maintained at 160° F (71°C). The test liquids are listed below and include diesel fuel and various commercially available additives for diesel fuel alone and mixed with diesel fuel. At intervals, the samples were removed, cooled to 25°C and dried, and their resistance measured. Table 3 shows the value of the ratio R f/ R i for the different samples at various times. The additives tested, and their main ingredients, were as follows:
- compositions of Examples 7-15 were tested by the following tests. Samples 1 inch (2.54cm) by 1.5 inch (3.8 cm) were cut from the molded slabs. Electrodes were formed on each sample by painting a strip 0.25 inch (0.62 cm) wide at each end with a suspension of silver particles (Electrodag 504 available from Acheson Colloids). The samples were annealed for 5 minutes at 200°C, and then cooled. The samples were then placed in an oven at 100°C and their resistances measured at intervals. It was found at the lower the head-to-head content of the polymer, the less its change in resistance.
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- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Ceramic Engineering (AREA)
- Electromagnetism (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Conductive Materials (AREA)
- Thermistors And Varistors (AREA)
- Resistance Heating (AREA)
- Air-Conditioning For Vehicles (AREA)
- Wick-Type Burners And Burners With Porous Materials (AREA)
Abstract
Description
- This invention relates to conductive polymer compositions and devices comprising them.
- Conductive polymer compositions, and devices comprising them, are known or are described in copending patent applications. Reference may be made for example to U.S. Patents Nos. 2,978,665, 3,243,753, 3,351,882, 3,571,777, 3,793,716, 3,823,217, 3,861,029, 4,017,715, 4,177,376, 4,188,276, 4,237,441, 4,238,812, 4,242,573, 4,246,468, 4,255,698, 4,272,471 and 4,276,466; U. K. Patent No. 1,534,715; J. Applied Polymer Science 19, 813-815 (1975), Klason and Kubat; Polymer Engineering and Science 18, 649-653 (1978) Narkis et al; and German OLS Nos. 2,634,999, 2,755,077, 2,746,602, 2,755,076, 2,821,799, 2,949,173 and 3,030,799; European Published Patent Applications Nos. 0,026,571, 0,028,142, 0,030,479, 0,038,713, 0,038,714, 0,038,715, 0,038,716, 0,038,717 and 0,038,718; and the copending applications corresponding to U.S. Serial Nos. 150,909, and 254,352 and U.K. Applications Nos. 2,075,992A, 2,080,834A, 8209923, 8217000, 8216999 and 8216997. The disclosure of each of the patents, publications and applications referred to above is incorporated herein by reference.
- Electrical devices containing conductive polymers generally (though not invariably) comprise an outer jacket, usually of insulating material, to protect the conductive polymer from damage by the surrounding environment. However, if no protective jacket is used, or if the jacket is permeable to harmful species in the environment, or if the conditions of use are such that the jacket may become damaged, it is necessary or desirable to select a conductive polymer which is not damaged (or which deteriorates at an acceptably low rate) when exposed to the surrounding environment. Exposure of conductive polymers to organic fluids generally results in an increase in resistivity; exposure to air, especially at elevated temperatures between room temperature and 35°C below the melting point generally results in a decrease in resistivity both at the elevated temperature and at room temperature (a phenomenon known in the art as "resistance relaxation").
- We have discovered that conductive polymer compositions which are based on polyvinylidene fluoride exhibit substantially improved stability if the polyvinylidene fluoride has a very regular structure which can be characterized by a low head-to-head content in the repeating units. Polyvinylidene fluoride is made up of repeating units of formula -CH2CF2-, which can be arranged head-to-tail (i.e. - CH2CF2-CH2CF2-) or head-to-head (i.e. -CH2CF2-CF2CH2-), and we have found that the lower the head-to-head content, the greater the stability of the resistivity of the composition when exposed to organic fluids and/or when exposed to air at elevated temperature. Previously known conductive polymer compositions based on polyvinylidene fluoride have made use of polyvinylidene fluoride of relatively high head-to-head content, namely at least 5.2% and generally higher, which are easier to process than the polymers used in the present invention.
- In its first aspect, the present invention provides a conductive polymer composition which comprises (a) polyvinylidene fluoride having a head-to-head content of less than 5.0%, preferably less than 4.5%, particularly less than 4.0%, and (b) a particulate conductive filler, especially carbon black, dispersed in the polyvinylidene fluoride. The composition preferably exhibits PTC behavior.
- In its second aspect, the invention provides an electrical device which comprises a conductive polymer element composed of a conductive polymer composition as defined above and at least one electrode in electrical contact with said element, for example, at least two electrodes which can be connected to a source of electrical power and which when so connected cause current to flow through the conductive polymer element. Preferred devices are self-limiting heaters, e.g. flexible strip heaters, in which the conductive polymer composition exhibits PTC behavior. Such heaters are particularly useful for heating liquids in which the heater is immersed, especially diesel fuel (see U.K. applications Nos. 8216999 and 8216997.
- In a third aspect, the invention provides a method of heating a liquid, particularly an organic liquid, especially diesel fuel, which comprises passing current through a self-limiting heater as defined above which is immersed in the liquid.
- In a fourth aspect the invention provides a fuel feedthrough and heating assembly which can be positioned and connected between a fuel filter and a fuel tank of a fuel supply system to provide means for heating fuel which is being pumped through a fuel line from the fuel tank to the fuel filter, said feedthrough and heating assembly comprising
- (A) a feedthrough comprising (i) a fuel conduit having at one end thereof a fuel line connector for connecting the feedthrough to a fuel line and at the other end thereof a fuel filter connector for connecting the feedthrough to a fuel filter; and (ii) a neck portion which protrudes from the fuel conduit between the ends thereof and which comprises a chamber;
- (B) a flexible self-limiting strip heater as defined above which preferably comprises a fuel-resistant insulating jacket, one end of the strip heater being within the chamber of the neck portion, and the strip heater passing through the fuel line connector and protruding from the fuel conduit;
- (C) insulated electrical leads connected to the electrodes of the heater, the connections lying within the chamber of the neck portion;
- (D) a fuel-resistant, water-resistant and insulating composition which encapsulates (i) the connections between the electrodes and the leads, (ii) the insulation at the ends of the connected electrical leads and (iii) the insulating jacket at the end of the connected heater; and
- (E) a fuel-resistant gasket which prevents fuel which is being pumped through the fuel conduit from exiting through the neck portion.
- Polyvinylidene fluorides suitable for use in this invention are commercially available. The head-to-head content of a polyvinylidene fluoride can be measured by those skilled in the art. We have found that the measured head-to-head contents of different samples of a polymer sold under & particular trade name can differ substantially. In general, the presently available polyvinylidene fluorides made by suspension polymerization (rather than emulsion polymerization) have lower head-to-head contents. The number average molecular weight of the polymer is generally at least 5,000, eg. 7,000 to 15,000.
- The polyvinylidene fluoride is preferably a homopolymer of vinylidene fluoride, but the presence of small quantities of comonomers, (preferably less than 15%, particularly less than 5% by weight), eg. tetrafluoroethylene, hexafluoropropylene and ethylene, is not excluded. The polyvinylidene fluoride is preferably the sole crystalline polymer in the composition, but other crystalline polymers, eg. other crystalline fluoropolymers, may also be present. The composition may contain relatively small amounts (preferably less than 35%, especially less than 20%, particularly less than 10%, by volume)-of one or more elastomeric polymers, particularly solvent-resistant fluorine-containing elastomers and acrylic elastomers, which are usually added primarily to improve the flexibility and elongation of the composition.
- The particulate conductive filler preferably comprises carbon black, and often consists essentially of carbon black. Choice of the carbon black will influence the resistivity/temperature characteristics of the composition. Compositions exhibiting PTC behavior are preferred for many devices of the invention, especially self-limiting heaters, and for these a carbon black having a ratio of surface area (m2/g) to particle size (mu) of 0.03 to 6.0 is preferred. For other uses, compositions exhibiting ZTC or NTC behavior may be preferred. The amount of conductive filler used will depend upon the desired resistivity of the composition. For flexible strip heaters which are to be used for heating diesel fuel and powered by a 12 volt battery, we prefer a PTC composition whose resistivity at 25°C is less than 200 ohm.cm eg. about 10 to about 100 ohm.cm. In such compositions the amount of carbon black may for example be 16 to 25% by weight.
- In addition to one or more conductive fillers, the compositions may also comprise other conventional additives, such as non-conductive fillers (including flame retardants), antioxidants and crosslinking agents (or residues thereof if the composition has been cross-linked).
- The compositions of the invention are preferably cross-linked (particularly by irradiation), since this has been found to enhance their resistance to organic solvents.
- Preparation of the compositions of the invention can be carried out in conventional fashion. Often it will be convenient to melt-extrude the composition directly into a water bath (which may be heated), and using this technique subsequent annealing is often not required.
- The invention is illustrated by the following Examples, in which Examples 1, 2, 3, 7, 12 and 13 are Comparative Examples not in accordance with the invention.
- The ingredients listed for Composition A in-Table 1 below were mixed in a Banbury mixer. The mixture was dumped, placed on a steam-heated mill and extruded into a water bath through a 3.5 inch (8.9 cm) extruder fitted with a pelletizing die. The extrudate was chopped into pellets which were dried for 16 hours at 80°C.
- The ingredients listed for Composition B in Table 1 were mixed and'pelletized in the same way as for Composition A.
- 83% by weight of the Composition A pellets and 17% by weight of the Composition B pellets were tumble blended and dried at 110°C. The composition of the resulting Final Blend is shown in Table 1. Using a 1.5 inch (3.8 cm) diameter extruder fitted with a crosshead die having an orifice 0.4 inch (1.0 cm) x 0.1 inch (0.3 cm), the blend was melt-extruded over a pair of pre-heated 14 AWG (1.85 mm diameter) 19/27 nickel-coated copper wires with a center-to-center separation of 0.25 inch (0.64 cm).m. The extrudate was passed immediately through a bath of water at room temperature, air-dried, and then irradiated to a dosage of 10 Mrad. The conductive polymer had a resistivity of about 50 ohm.cm at 25°C.
-
- Kynar 460 is polyvinylidene fluoride available from Pennwalt and having a head-to-head content of about 5.5%.
- Furnex N765 is a carbon black available from Columbia Chemical having a particle size of about 60 millimicrons, a surface area of about 32 m2/g and a DBP value of about 112 cm3/100 g.
- Viton AHV is a copolymer of hexafluoropropylene and polyvinylidene fluoride manufactured by du Pont.
- Omya-BSH is calcium carbonate available from Omya Inc.
- TAIC is triallyl isocyanurate, a radiation cross-linking agent.
- The ingredients listed for Examples 2 to 6 in Table 2 below were mixed in a Banbury mixer. The mixture was dumped, granulated and dried for 72 hours at 75°C under vacuum. Using a 0.75 inch (1.9 cm) single screw extruder fitted with a cross-head die having an orifice 0.3 inch (0.76 cm) x 0.1 inch (0.3 cm), the blend was melt-extruded over a pair of pre-heated 18 AWG (1.2 mm diameter) 19/27 nickel-coated copper wires with a center-to-center separation of 0.25 inch (0.64cm). The extrudate was passed immediately through a bath of water at room temperature, air-dried, and then irradiated to a dosage of 10 Mrad.
- The ingredients shown for Examples 7-15 in Table 2 were mixed in a Banbury mixer, dumped and then granulated. The granulated materials were molded into slabs of thicknesses of 0.030" (0.076 cm) to 0.036" (.091 cm) by compression molding at 200*C for three minutes.
ynar 450 is polyvinylidene fluoride available from Pennwalt and having a head-to-head content in the range 5.5 to 6.3. - Solef-1010 is a polyvinylidene fluoride available from Solvay et cie of Belgium, and having a head-to head content of 4.1%.
- KF1000 and KF1100 are polyvinylidene fluorides available from Kureha Chemical Industry Co. of Japan, and having a head-to-head content of 3.5 to 3.8%.
- Statex G is a carbon black available from Cities Services Co., Columbian Division having a particle size of about 60 millimicrons, a surface area of about 32 m2/g and a DBP value of about 90 cm3/100 g.
- Dyflor 2000 M is a polyvinylidene fluoride available from Kay-Fries, Inc., member of Dynamit Nobel Chemikalien of Federal Republic of Germany and having a head-to-head content of about 4.4-4.9.
- Vulcan XC-72 is a carbon black available from Cabot Co., having a particle size of about 30 millimicrons, a surface area of about 224 m2/g and a DBP value of about 178 cm3/100 g.
- The extrudates obtained in Examples 1 and 4 were compared by the following tests. Samples 2 inch (5.1 cm) long were cut from the extrudates. The samples were immersed in various solvents at 25°C and the resistance of the samples was measured at intervals. The solvents used, and their solubility parameters, were
- The extrudates obtained in Examples 1 to 6 were compared in the following way. Samples 2 inch (5.1 cm) long were cut from the extrudates and were immersed in various test liquids maintained at 160° F (71°C). The test liquids are listed below and include diesel fuel and various commercially available additives for diesel fuel alone and mixed with diesel fuel. At intervals, the samples were removed, cooled to 25°C and dried, and their resistance measured. Table 3 shows the value of the ratio Rf/Ri for the different samples at various times. The additives tested, and their main ingredients, were as follows:
- B12 Toluene, methanol, acetone, naphthalenic mineral oil and ethylene glycol monobutylether.
-
Fire Prep 100 Naphthalenic oil and partly oxidised aliphatic hydrocarbon - Sta-Lube Naphthalenic mineral oil
- Redline Naphthalenic mineral oil, barium carbonate and
- Catalyst other inorganic carbonates, and sulfur-containing material
- Wynn's Naphthalenic mineral oil/and isopropanol Conditioner
- Gumout Naphthalenic mineral oil, non-aromatic ester and aliphatic acid.
- Wynn's --Naphthalenic mineral oil, non-aromatic ester,
- Anti- aliphatic amide, and aliphatic acid. Knock
- FPPF Ethyl cellulose, ethylene glycol monobutylether, and oxidised hydrocarbons.
-
- The compositions of Examples 7-15 were tested by the following tests. Samples 1 inch (2.54cm) by 1.5 inch (3.8 cm) were cut from the molded slabs. Electrodes were formed on each sample by painting a strip 0.25 inch (0.62 cm) wide at each end with a suspension of silver particles (Electrodag 504 available from Acheson Colloids). The samples were annealed for 5 minutes at 200°C, and then cooled. The samples were then placed in an oven at 100°C and their resistances measured at intervals. It was found at the lower the head-to-head content of the polymer, the less its change in resistance.
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT82304744T ATE35745T1 (en) | 1981-09-09 | 1982-09-09 | HEATING DIESEL FUEL. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30070981A | 1981-09-09 | 1981-09-09 | |
US300709 | 1981-09-09 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0074281A1 true EP0074281A1 (en) | 1983-03-16 |
EP0074281B1 EP0074281B1 (en) | 1988-07-13 |
Family
ID=23160253
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82304744A Expired EP0074281B1 (en) | 1981-09-09 | 1982-09-09 | Heating diesel fuel |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0074281B1 (en) |
JP (2) | JPS5853939A (en) |
AT (1) | ATE35745T1 (en) |
CA (1) | CA1236246A (en) |
DE (1) | DE3278775D1 (en) |
GB (1) | GB2106920B (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4571481A (en) * | 1983-03-11 | 1986-02-18 | Raychem Corporation | Method and apparatus for electrically heating diesel fuel |
EP0217512A1 (en) * | 1985-08-12 | 1987-04-08 | RAYCHEM CORPORATION (a Delaware corporation) | Polymer thick film inks |
AU571798B2 (en) * | 1985-09-18 | 1988-04-21 | Yasuda, S. | Heat sensitive - electrically resistant polymer composition |
EP0388990A2 (en) | 1986-02-20 | 1990-09-26 | RAYCHEM CORPORATION (a Delaware corporation) | Method and articles employing ion exchange material |
EP1205514A1 (en) * | 2000-11-13 | 2002-05-15 | Atofina | Polymeric conducting composite material whose resistance is automatically controlled by the temperature |
FR2816625A1 (en) * | 2000-11-13 | 2002-05-17 | Atofina | Composite material with a positive temperature coefficient, useful in heating devices, comprises a vinylidene fluoride (co)polymer in beta crystal form and a conductive filler |
US8618203B2 (en) | 2003-02-19 | 2013-12-31 | Dupont-Mitsui Fluorochemicals Co., Ltd. | Fluoropolymer composite composition |
WO2014168904A1 (en) * | 2013-04-10 | 2014-10-16 | E. I. Du Pont De Nemours And Company | Polymer thick film positive temperature coefficient carbon composition |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1236246A (en) * | 1981-09-09 | 1988-05-03 | Raychem Corporation | Electrically conductive polyvinylidene fluoride compositions |
US4861966A (en) * | 1985-10-15 | 1989-08-29 | Raychem Corporation | Method and apparatus for electrically heating diesel fuel utilizing a PTC polymer heating element |
JPH0799721B2 (en) * | 1986-09-13 | 1995-10-25 | 日本メクトロン株式会社 | Method for producing PTC composition |
US5174924A (en) * | 1990-06-04 | 1992-12-29 | Fujikura Ltd. | Ptc conductive polymer composition containing carbon black having large particle size and high dbp absorption |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1805906A1 (en) * | 1967-11-20 | 1969-06-19 | Pennsalt Chemicals Corp | Heat stabilized polyvinyl fluoride |
FR2443123A1 (en) * | 1978-12-01 | 1980-06-27 | Raychem Corp | LOW RESISTIVITY COMPOSITION AND DEVICE CONTAINING THE SAME |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55111183A (en) * | 1979-02-20 | 1980-08-27 | Ngk Spark Plug Co Ltd | Piezoelectric high-molecular compound material |
DE2928081C2 (en) * | 1979-07-12 | 1982-08-19 | Glyco-Metall-Werke Daelen & Loos Gmbh, 6200 Wiesbaden | Laminated composite material and process for its manufacture |
EP0068688A3 (en) * | 1981-06-15 | 1983-05-25 | RAYCHEM CORPORATION (a California corporation) | Fuel line heater feedthrough |
CA1236246A (en) * | 1981-09-09 | 1988-05-03 | Raychem Corporation | Electrically conductive polyvinylidene fluoride compositions |
-
1982
- 1982-09-08 CA CA000410978A patent/CA1236246A/en not_active Expired
- 1982-09-09 EP EP82304744A patent/EP0074281B1/en not_active Expired
- 1982-09-09 AT AT82304744T patent/ATE35745T1/en not_active IP Right Cessation
- 1982-09-09 JP JP57157941A patent/JPS5853939A/en active Granted
- 1982-09-09 DE DE8282304744T patent/DE3278775D1/en not_active Expired
- 1982-09-09 GB GB08225680A patent/GB2106920B/en not_active Expired
-
1990
- 1990-08-02 JP JP2206677A patent/JPH0395248A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1805906A1 (en) * | 1967-11-20 | 1969-06-19 | Pennsalt Chemicals Corp | Heat stabilized polyvinyl fluoride |
FR2443123A1 (en) * | 1978-12-01 | 1980-06-27 | Raychem Corp | LOW RESISTIVITY COMPOSITION AND DEVICE CONTAINING THE SAME |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4571481A (en) * | 1983-03-11 | 1986-02-18 | Raychem Corporation | Method and apparatus for electrically heating diesel fuel |
EP0217512A1 (en) * | 1985-08-12 | 1987-04-08 | RAYCHEM CORPORATION (a Delaware corporation) | Polymer thick film inks |
US4722853A (en) * | 1985-08-12 | 1988-02-02 | Raychem Corporation | Method of printing a polymer thick film ink |
AU571798B2 (en) * | 1985-09-18 | 1988-04-21 | Yasuda, S. | Heat sensitive - electrically resistant polymer composition |
EP0388990A2 (en) | 1986-02-20 | 1990-09-26 | RAYCHEM CORPORATION (a Delaware corporation) | Method and articles employing ion exchange material |
EP1205514A1 (en) * | 2000-11-13 | 2002-05-15 | Atofina | Polymeric conducting composite material whose resistance is automatically controlled by the temperature |
FR2816625A1 (en) * | 2000-11-13 | 2002-05-17 | Atofina | Composite material with a positive temperature coefficient, useful in heating devices, comprises a vinylidene fluoride (co)polymer in beta crystal form and a conductive filler |
US8618203B2 (en) | 2003-02-19 | 2013-12-31 | Dupont-Mitsui Fluorochemicals Co., Ltd. | Fluoropolymer composite composition |
WO2014168904A1 (en) * | 2013-04-10 | 2014-10-16 | E. I. Du Pont De Nemours And Company | Polymer thick film positive temperature coefficient carbon composition |
US9573438B2 (en) | 2013-04-10 | 2017-02-21 | E I Du Pont De Nemours And Company | Polymer thick film positive temperature coefficient carbon composition |
Also Published As
Publication number | Publication date |
---|---|
ATE35745T1 (en) | 1988-07-15 |
CA1236246A (en) | 1988-05-03 |
GB2106920A (en) | 1983-04-20 |
JPH0334498B2 (en) | 1991-05-22 |
DE3278775D1 (en) | 1988-08-18 |
GB2106920B (en) | 1985-06-26 |
JPH0395248A (en) | 1991-04-19 |
EP0074281B1 (en) | 1988-07-13 |
JPS5853939A (en) | 1983-03-30 |
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