[0001] The invention relates to a mesophase pitch derived carbon fibre and particularly
to a carbon fibre which has been boro-rated and intercalated with calcium.
[0002] It is well known to spin a mesophase pitch into a fibre, thermoset the pitch fibre
by heating it in air, and carbonize the thermoset pitch fibre by heating the thermoset
pitch fibre in an inert gaseous environment to an elevated temperature.
[0003] It is preferable to use mesophase pitch rather than isotropic pitch for producing
the carbon fibres because the mesophase pitch derived carbon fibre possesses excellent
mechanical properties. Furthermore, it is preferable to use a mesophase pitch having
a meshophase content of at least about 70% by weight for the process.
[0004] Carbon fibres have found a wide range of commercial uses. In certain uses, it is
desirable to use carbon fibres which possess both excellent mechanical properties
and good electrical conductivity. The electrical conductivity is usually described
in terms of resistivity. Typically, a mesophase pitch derived carbon fibre which has
been carbonized to a temperature of about 2500°C has a resistivity of about 7 microohm-metres
and a Young's modulus of about 413.6 GPa. The same carbon fibre heat treated to about
3000°C has a resistivity of about 3.3 microohm-metres.
[0005] The cost for obtaining temperatures of 2500°C and particularly 3000°C is very high.
Not only is it closely to expend the energy to reach the high temperatures, but the
equipment needed to reach such high temperatures is costly and deteriorates rapidly
due to the elevated temperatures.
[0006] The present invention allows the production of a mesophase pitch derived carbon fibre
having'a resistivity of less than about 2 microohm-metres,and preferably about 1 microohm-metre,
with a maximum heat treating temperature of from about 2000°C to about 2300°C.
[0007] The present invention relates to a mesophase pitch derivated carbon fibre which has
been boronated and intercalated with calcium.
[0008] In the preferred embodiment there is a calcium to boron weight ratio of about 2:1
in the carbon fibre.
[0009] In the absence of boron, the calcium does not intercalate into the carbon fibhe very
well. Even very small amounts of boron enhance the intercalation of the calcium. Generally,
0.1% by weight boron or even less is sufficient to improve substantially the intercalation
of calcium into the carbon fibres.
[0010] For any given amount of boron in a carbon fibre, the resistivity generally increases
as the amount of intercalated calcium increases at the low end, below a calcium to
boron weight ratio of 2:1. It is believed that the boron acts as an acceptor and the
calcium acts as an electronic donor. The interaction between the boron and the calcium
is such that a maximum resistivity is reached and then the resistivity is reduced
until a minimum is reached for a calcium to boron weight ratio of about 2:1. Apparently
high conductivity is associated with the donor state. As the amount of calcium increases
so that the ratio is greater than 2:1, the resistivity increases because a multiple
phase condition exists.
[0011] Generally, if one were to boronate a carbon fibre in the absence of. calcium, the
maximum amount of boron which could be introduced into the carbon fibre is about 1.2%
by weight. The presence of the intercalcated calcium, however, substantially increases
the maximum amount of boron. It is expected that about 10% by weight or more of boron
can be introduced into the carbon fibre in the presence of the intercalated calcium.
In addition, it is expected that as much as 20% by weight of calcium can be intercalated
into the carbon fibre in the presence of the boron.
[0012] Surprisingly, the boron and calcium can be introduced into the carbon fibre without
chemically reacting with the carbon fibre so that a single phase is maintained. Heat
treatments at elevated temperatures can result in the formation of new phase, calcium
borographite.
[0013] It is believed that the presence of the intercalated calcium results in cross-linking
between layer -planes in the carbon fibre and improved mechanical properties are obtained.
Excellent values for tensile strength and Young's modulus are obtained for the calcium
intercalated boronated fibres even though relatively low process temperatures are
used. For example, a carbon fibre according to the invention which has been produced
using a process temperature of about 2000°C possesses mechanical properties comparable
to a conventional mesophase pitch derived carbon fibre which has been subjected to
a process temperature of 3000°C. In addition, the carbon fibre according to the invention
possesses much lower resistivity compared to the conventional carbon fibre.
[0014] Surprisingly, the carbon fibre according to the invention possesses a relatively
high interlayer spacing as compared to the typical interlayer spacing of 3.37 Angstroms
of a carbon fibre which has been subjected to a heat treatment of about 3000°C. According
to the prior art, one would expect a deterioration of mechanical properties for larger
values of interlayer spacing for the carbon fibres. The maximum interlayer spacing
occurs for a calcium to boron weight ratio of about 2:1 as in the case for the minimum
resistivity.
[0015] Generally, about 0.5% by weight boron and about 1% by weight calcium provides a good
quality carbon fibre according to the invention.
[0016] The present invention also relates to a method of producing a meshophase pitch derived
carbon fibre having a low resistivity and excellent mechanical properties, and comprises
the steps of boronating and intercalating with calcium,a carbon fibre having a diameter
of less than 30 microns and derived from a mesophase pitch having a mesophase content
of at least about 70% by weight mesophase.
[0017] The steps for boronating and intercalating can be carried out simultaneously or consecutively,
boronating being first.
[0018] The preferred embodiment is to carry out the method to produce a calcium intercalated
boronated carbon fibre having a calcium to boron weight ratio of about 2:1.
[0019] The boronating can be carried out with elemental boron, boron compounds, or a gaseous
boron compound. A calcium compound such as for example CaNCN can be used. Oxygen-containing
compounds of calcium are less desirable because of the possible detrimental effect
of the oxygen on the carbon fibre.
[0020] Boronating up to about 1.2% by weight maintains a single phase in the carbon fibre.
Greater amounts of boron tend to produce boron carbide, B
4C,
[0021] In carrying out the present invention, the carbon fibre has a diameter of less than-30
microns and preferably about 10 microns.
[0022] Further objects and advantages of the invention will be set forth in the following
specification and in part will be obvious therefrom without specifically being referred
to, the same being realized and attained as pointed out in the claims hereof.
[0023] Illustrative, non-limiting Examples of the practice of the invention are set out
below. Numerous other examples can readily be evolved in the light of the guiding
principles and teachings contained herein. The examples given herein are intended
to illustrate the invention and not in any sense limit the manner in which the invention
can be practiced.
[0024] The Examples were carried out using mesophase pitch derived carbon fibres having
diameters of about 8 microns. The mesophase pitch used to produce the fibres had a
mesophase content of about 80% by weight.
[0025] The carbon fibres were produced using conventional methods and were carbonized to
about 1700°C. Lower or higher carbonizing temperatures could have been used. The use
of carbon fibres made the handling of the fibres simple because of the mechanical
properties exhibited by carbon fibres.
[0026] The best mode used in the Examples simultaneously boronated and calcium intercalated
the carbon fibres. This does not preclude the advantage of consecutive treatments
for commercial operations. The method used is as follows.
[0027] Finely ground graphite, so-called graphite flour, was blended with elemental boron
powder. The weight percentage of boron was selected to about the desired weight percentage
for the carbon fibres. This mixture amounted to about 600 grams and was roll-milled
for about 4 hours to mix and grind the graphite and boron thoroughly. The mixture
was then calcined in an argon atmosphere at a temperature of about 2500°C for about
one hour. Any inert atmosphere would have been satisfactory.
[0028] The boronated graphte flour was blended with CaNCN powder having particles less than
about 44 microns to form a treatment mixture. The amount of CaNCN is determined by
the amount of calcium to be intercalated.
[0029] The weight of the carbon fibres being treated as compared to the amount of the treatment
mixture used is very small. As a result, the weight percentage of the boron in the
treatment mixture is about the same for the combination of the carbon fibres and the
treatment mixture. This simplifies the selection of a predetermined weight percentage
of boronating for the carbon fibres.
[0030] The amount of calcium intercalation must be determined experimentally by varying
the-amount of the calcium compound used and the treatment time.
[0031] It should be recognized that the vapour pressure of the boron is much lower than
the.calcium. The boronation is a result of atomic diffusion whereas the intercalation
of calcium is a result of vapour diffusion.
[0032] For each Example, six carbon fibres were used and each fibre had a length of about
1-0 cm. Each of the carbon fibres was suspended inside a graphite container using
a graphite form. The graphite form maintained the carbon fibre in a preselected position
while the treatment mixture was added to the graphite container. The treatment mixture
was vibrated around each carbon fibre to obtain a uniform and packed arrangement.
[0033] The six graphite containers were placed in a graphite susceptor and heated inductively
to a predetermined maximum temperature for about 15 minutes. The furnace chamber was
evacuated to about 5 x 10
-5 Torr prior to the heat treatment and then purged with argon during the heating cycle.
An inert gas other than argon could be used.
[0034] The process could be carried out using BC1
3, boranes or water-soluble salts such as H
3B0
3. In addition,CaC1
2 could have been used. Of course, a wide range of other compounds for supplying boron
and calcium could be realized easily experimentally in accordance with the criteria
set forth herein.
Examples 1 to 18:
[0035] Examples 1 to 18 were carried out to obtain about 0.5% by weight of boron in the
carbon fibres and varying amounts of intercalated calcium. The maximum temperature
for the heat treatment was 2050°C.
[0036] Table 1 shows the results of Examples 1 to 18. The amount of the intercalated calcium
varied from about 0.5% to about 3.6% by weight. The Young's modulus for each of the
carbon fibres was extremely high and the tensile strength was also very good. The
resistivity showed a minimum of about 1.8 microohm-metres for about 1% by weight calcium
the interlayer spacing, Co/2 was about a maximum for that value.
[0037]

Examples 19 to 40
[0038] Examples 19 to 40 were carried out to obtain about 1.0% by weight of boron in the
carbon fibres and varying amounts of intercalated calcium. The maximum temperature
for the heat treatment was 2050°C.
[0039] Table 2 shows the results of Examples 19 to 40. By interpolation, it can be seen
that as in Examples 1 to 18, a calcium to boron weight ratio of 2:1 results in the
lowest resistivity, about 1.1 microohm-metres, and a large value for the interlayer
spacing.
[0040]

Examples 41 to 58:
[0041] Examples 41 to 58 were carried out to obtain about 2.0% by weight of boron in the
carbon fibres and varying amounts of intercalated calcium. The maximum temperature
for the heat treatment was 1600°C..
[0042] Table 3 shows the results of Examples 41 to 58.
[0043] The values of the resistivity are not as good as in Examples 1 to 40. The lowest
resistivity is for a calcium to boron weight ratio of about 2:1. The value for the
Young's modulus for each carbon fibre is fairly high.
[0044]

Examples 59 to 75:
[0045] Examples 59 to 75 were carried out to obtain about 2.0% by weight of boron in the
carbon fibres as in Examples 41 to 58 except that the maximum temperature for the
heat treatment was 2050°C.
[0046] Table 4 shows the results of Examples 59 to 75.
[0047] Examples 59 to 75 produced much lower values for resistivity than Examples 41 to
58. The lowest resistivity and highest interlayer spacing can be interpolated to be
at a calcium to boron weight ratio of about 2:1. The Young's modulus and tensile strength
for each of the carbon fibres is excellent.

Examples 76 to 93:
[0048] Examples 76 to 93 were carried out to obtain about 2.0% by weight of boron in the
carbon fibres as in Examples 41 to 75 except that the maximum temperature for the
heat treatment was about 2300°C.
[0049] Table 5 shows the results of Examples 76 to 93.
[0050] Examples 76 to 93 compare well with Examples 59 to 75.

[0051] While a maximum temperature for the heat treatment can exceed 2300°C, there is a
reduction of mechanical properties of the fibres when the maximum temperature exceeds
2500°C.
Examples 94 to 109:
[0052] Examples 94 to 109 were carried out to obtain about 5% by weight of boron in the
carbon fibres. The maximum temperature for the heat treatment was about 2050°C.
[0053] Table 6 shows the results of Examples 94 to 109.
[0054] Examples 94 to 109 do not include the preferred calcium to boron weight ratio but
the trend of resistivity versus calcium content shows the characteristic increase
in resistivity for a calcium to boron weight ratio less than 2:1. In addition, the
interlayer spacing increases from a calcium content of about 3.8% to 8.5% by weight
and would be expected to be a maximum at about 10% by weight in accordance with the
invention.
[0055]

1. A mesophase pitch derived : carbon fibre having a diameter of less than 30 microns
and which has been boronated and intercalated with calcium.
2. A carbon fibre according to claim 1 wherein the calcium to boron weight ratio in
the fibre is about'2:1.
3. A carbon fibre according to claim 1 or 2 wherein said fibre contains at least about
0.1% by weight boron.
4. A carbon fibre according to claim 1, 2 or 3 wherein the resistivity of the fibre
is about one microohm-metre.
5. A carbon fibre according to any of claims 1 to 4 wherein the fibre contains up
to about 10% by weight boron and up to about 20% by weight calcium.
6. A method of producing a mesophase pitch derived carbon fibre comprising the steps
of boronating and intercalating with calcium a carbon fibre having a diameter of less
than 30 microns and derived from a mesophase pitch having a mesophase content of at
least about 70% by weight mesophase.
7. A method according to claim 6 wherein the boronating and intercalating steps are
carried out simultaneously, or the intercalating step is carried out subsequent to
the boronating step.
8. A method according to claim 6 or 7 wherein the boronating and intercalating steps
are carried out to produce a calcium to boron weight ratio of about 2:1 in said fibre.
9. A method according to claim 8 wherein the fibre contains at least about 0.1% by
weight boron.
10. A method according to any of claims 6 to 9 wherein the boronating step is carried out with elemental boron, BCl3, a borane or a water-soluble compound of boron.
11. A method according to any of claims 6 to 10, wherein the intercalating step is
carried out using CaNCN or CaC12.