[0001] This invention relates to conductive polymer compositions and devices comprising
them.
[0002] 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.
[0003] 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").
[0004] 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
-CH
2CF
2-, which can be arranged head-to-tail (
i.e. - CH
2CF
2-CH
2CF
2-) 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.
[0005] 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.
[0006] 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.
[0007] 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.
[0008] 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.
[0009] 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.
[0010] 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.
[0011] 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. 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.
[0012] 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).
[0013] The compositions of the invention are preferably cross-linked (particularly by irradiation),
since this has been found to enhance their resistance to organic solvents.
[0014] 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.
[0015] 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.
EXAMPLE 1
[0016] 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.
[0017] The ingredients listed for Composition B in Table 1 were mixed and'pelletized in
the same way as for Composition A.
[0018] 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.
[0019]

[0020] Kynar 460 is polyvinylidene fluoride available from Pennwalt and having a head-to-head
content of about 5.5%.
[0021] 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.
[0022] Viton AHV is a copolymer of hexafluoropropylene and polyvinylidene fluoride manufactured
by du Pont.
[0023] Omya-BSH is calcium carbonate available from Omya Inc.
[0024] TAIC is triallyl isocyanurate, a radiation cross-linking agent.
EXAMPLES 2-6
[0025] 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.
EXAMPLES 7-15
[0026] 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.
Kynar 450 is polyvinylidene fluoride available from Pennwalt and having a head-to-head
content in the range 5.5 to 6.3.
[0027] Solef-1010 is a polyvinylidene fluoride available from Solvay et cie of Belgium,
and having a head-to head content of 4.1%.
[0028] 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%.
[0029] 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.
[0030] 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.
[0031] 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
cm
3/
100 g.
TESTS FOR STABILITY IN ORGANIC SOLVENTS
[0032] 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.
[0033] 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:
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.
[0034]

RESISTANCE RELAXATION TESTS
[0035] 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.