Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
CA 02485232 2001-01-25
SPECIFICATION
POROUS CARBON ELECTRODE SUBSTRATE
TECHNICAL FIELD
The present invention relates to carbon fiber paper and
an electrode substrate for a fuel cell using the paper and more
particularly an electrode substrate for a solid polymer
electrolyte fuel cell and its production method.
BACKGROUND ART
As compared with an electrode for a phosphoric acid fuel
cell, an electrode for a solid polymer electrolyte fuel cell
is required to have gas diffusion-permeability,,strength to
be durable to handling, flexibility, strength to stand the
compression at the time of electrode production and electrode
assembly, and the like. Further, since the solid polymer
electrolyte fuel cell is required to be small in size, as
compared with a phosphoric acid fuel cell, the electrode for
it is also required to be thin. As the electrode for such a
solid polymer electrolyte fuel cell, mairily used are those
which are produced by forming paper from carbon short fibers,
impregnating the paper with a thermosetting resin, curing the
resin, and then carbonizing the resultant paper, and in order
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CA 02485232 2001-01-25
to improve the productivity of a fuel cell, the electrode has
to be flexible enough to be rolled in a roll. However, many
electrodes ever made available are thick and mostly easily
broken when being bent. Further, since those conventional
electrodes have a few contacting points of carbon fibers, they
have a problem that the conductivity becomes worse if the
porosity is increased.
A porous carbon electrode substrate provided with an
improved conductivity by mixing carbonaceous milled fibers is
described in Japanese Patent Laid-Open No. 142068/1995,
however the substrate is too thick in thickness and thus
insufficient in flexibility to be used for a solid polymer
electrolyte fuel cell.
Invention of a porous carbon plate and its production
method is described in Japanese Patent Laid-Open No.
157052/1997, the electrode of the invention has a low bulk
density and therefore it cannot be said that the conductivity
of the electrode is sufficient.
DISCLOSURE OF THE INVENTION
Objects of the present invention areto solve the above
described problems and provide an electrode substrate for a
fuel cell having high conductivity and flexibility, its
production method, and carbon fiber paper suitable for
producing the electrode substrate.
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CA 02485232 2001-01-25
The present invention provides carbon fiber paper
consisting of an organic high-molecular compound as a binder
and carbon fibers, the carbon fibers containing thin fibers
with an average diameter smaller than 5 m and an average fiber
length of 3 to 10 mm.
In the carbon fiber paper of the present invention, the
organic high-molecular compound is preferably polyvinyl
alcohol, and the organic high-molecular compound is preferably
pulp-like substances or short fibers of an acrylonitril,e type
polymer. Further, the foregoing carbon fibers are preferably
only of polyacrylonitrile type carbon fibers. Furthermore,
the foregoing carbon fibers are preferably a mixture of thin
fibers with an average diameter larger than 3 m and smaller
than 5 m and an average fiber length of 3 to 10 mm and 'thick
fibers with an average diameter not smaller than 5 m and smaller
than.9 nm and an average fiber length of 3 to 10 mm. It is
also preferable for the foregoing carbon fibers to contain not
less than 40% by mass of the foregoing thin fibers.
The present invention also provides a porous carbon
electrode substrate for a fuel cell having a thickness of 0.05
to 0. 5 mm and a bulk density of 0. 3 to 0. 8 g/cm3, and also having
a bending strength of 10 MPa or higher and a deflection of 1.5
mm or more at the time of bending, measured by a three-point
bending test in conditions of using a sample of 1 cm width,
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CA 02485232 2008-06-13
a strain rate of 10 mm/min and a distance between supporting
points of 2cm.
The invention further provides a porous carbon
electrode substrate for a fuel cell, said substrate having a
thickness of 0.05 to 0.5 mm and a bulk density of 0.3 to 0.8
g/cm3, and also having a bending strength of 40 MPa or
higher and a deflection of 1.5 mm or more at the time of
bending, measured by a three-point bending test in
conditions of using a sample width of 1 cm, a strain rate of
10 mm/min and a distance between supporting points of 2 cm,
and containing carbon fibers which are a mixture of thin
fibers with an average diameter larger than 3 pm and smaller
than 5 pm and an average fiber length of 3 to 10 mm and
thick fibers with an average diameter not smaller than 5 pm
and smaller than 9 pm and an average fiber length of 3 to 10
mm.
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The electrode substrate of the present invention
preferably has a length of 1 m or larger and can be rolled around
a roll with an outer diameter of 50 cm or smaller. Further,
it is preferred that the electrode substrate contains carbon
fibers, and the foregoing carbon fibers are only of
polyacrylonitrile type carbon fibers. Furthermore, it is
preferred that the electrode substrate contains carbon fibers,
and the carbon fibers are a mixture of thin fibers with an
average diameter larger than 3 m and smaller than 5 m and
an average fiber length of 3 to 10 mm and thick fibers with
an average diameter not smaller than 5 .m and smaller than 9
m and an average fiber length of 3 to 10 mm. It is also
preferable fortheelectrode substrateto contain carbon fibers
which contain not less than 40% by mass of the foregoing thin
fibers in the total carbon fibers.
The present invention also provides a method of producing
a porous carbon electrode substrate for a fuel cell by
impregnating carbon fiber paper consisting of an organic
high-molecular compound as a binder and carbon fibers with an
average diameter smaller than 5 m and an average fiber length
of 3 to 10 mm with a thermosetting resin, curing the
thermosetting resin by heating and pressing treatment, and then
carbonizing the resultant paper.
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CA 02485232 2001-01-25
In the production method of the present invention, it is
preferable to use carbon fiber paper, amon.gthe above described
carbon fiber paper, wherein the carbon fibers are made of a
mixture of thin.fibers with an average diameter larger than
3 m and smaller than 5 pm and an average fiber length of 3
to 10 mm and thick fibers with an average diameter not smaller
than 5 pm and smaller than 9}.tm and an average fiber length
of 3 to 10 mm. Further, the foregoing heating and pressing
treatment is preferably carried out continuously in the whole
length of the carbon fiber paper. Further, prior to the heating
and pressing treatment, the carbonfiber paper impregnated with
the thermosetting resin is preferably pz-e-heated.
Furthermore, the heating and pressing treatment is preferably
carried out using a continuous type hot press machine equipped
with a pair of endless belts, or the heating and pressing
treatment is preferably carried out using a continuous type
hot roll press machine. In the heating and pressing treatment,
the pressure application is preferable to be carried out at
a line pressure of 1.5 x 109 to 1 x 105 N/m.
In the production method of the present invention, the
foregoing carbonization is preferably carried out
continuously in the whole length of the carbon fiber paper.
Further, the electrode substrate obtained by the foregoing
carbonization is preferable to be rolled around a roll with
the outer diameter of 50 cm or smaller. Furthermore, a
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CA 02485232 2001-01-25
conductive substance is preferably added to the foregoing
thermosetting resin.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 shows an example of a continuous type hot roll press.
machine suitable to be used for the production method of the
present invention; and
FIG. 2 shows an example of a continuous type hot press
machine equipped with a pair of endless belts and suitable to
be used for the production method of the present invention.
1 ... resin-impregnated carbon fiber paper, 2 ... mold release
agent-coated substrate, 3a, 3b ... endless belts, 4....
preheating zone, 5 ... heating and pressing zone
BEST MODE FOR CARRYING OUT THE INVENTION
J Hereinafter, the present invention will more particularly
be described.
The carbon fiber paper of the present invention consists
of carbon fibers containing thin carbon fibers with an average
diameter smaller than 5 m and an average fiber length of 3
to 10 mm and an organic high-molecular coinpound as a binder..
In the present invention, by using carbon short fibers
with an average diameter smaller than 5 m, preferably larger
than 3 m and not larger than 4. 5 E.zrn, the bending strength and
the flexibility of the porous electrode substrate can be
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CA 02485232 2001-01-25
improved. In the case of using only thick carbon fibers with
an average diameter larger than 5 m, the flexibility becomes
insufficient and the contacting points among fibers are too
small in number, and the resistance of an electrode produced
from such carbon fiber paper becomes too high. Further, by
making an average diameter larger than 3 m, the carbon fiber
paper is made dense and is capable of preventing the decrease
of gas permeability and therefore it is preferable.
Further, an average fiber length of the carbon fibers is
preferable to be 3 to 10 mm and further preferable to be 3 to
9 mm in terms of the strength and the smoothness of a substrate.
In the case where an average fiber length is smaller than 3
mm, the fibers are less entangled to result in decrease of the
strength of the substrate. On the other hand, in the case of
exceeding 10 mm, the dispersibility of fibers in a dispersant
is decreased to result in formation of uneven carbon fiber
paper.
The foregoing thin fibers with an average diameter smaller
than 5 u.m and an average fiber length of 3 to 10 mm are preferable
to.be not less than 40% by mass in the total carbon fibers..
That is, mixed carbon fibers can be used as the carbon fibers
of the present invention, the mixed carbon fibers being a
mixture of 40% by mass or more of thin fibers with an average
diameter smaller than 5 m and an average fiber length of 3
to 10 mm and 60% by mass or less of carbon fibers with an average
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CA 02485232 2001-01-25
diameter not smaller than 5 m in the total carbon fibers. In
order to maintain flexibility and high conductivity of an
electrode substrate, it is preferable to contain not less than
40% by mass of the foregoing thin fibers with an average
diameter smaller than 5 m in the mixed carbon fibers.
Other than the carbon fibers with an average fiber diameter
smaller than 5 m and an average fiber length of 3 to 10 mm,
carb.on fibers with an average fiber diameter not smaller than
5 m are preferable to be used and carbon fibers with an average
fiber diameter not smaller than 7 m are further preferable
to be used.
The carbon fibers contained in the carbon fiber paper are
also preferably a mixture of thin fibers with an average
diameter larger than 3 m and smaller than 5 pm and an average
fiber length of 3 to 10 mm and thick fibers with an average
diameter not smaller than 5 m and smaller than 9 m and an
average fiber length of 3 to 10 mm. The carbon fibers with
the thin diameter contribute to the improvement of flexibility
and conductivity of an electrode, whereas the carbon fibers
with the thick diameter contribute to the improvement of
dispersibility of the fiber substrate and gas permeability.
Consequently, carbon fiber paper produced by properly mixing
these fibers is provided with all of the above described
advantages and that is preferable.
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CA 02485232 2001-01-25
The carbon fibers to be used in the present invention may
be any of polyacrylonitrile type carbon fibers, pitch type
carbon fibers, rayon type carbon fibers, and the like. However,
polyacrylonitrile type carbon fibers, which have a relatively
high mechanical strength are preferable and particularly, it
is preferable that carbon fibers to be used are solely
polyacrylonitrile type carbon fibers.
The ol acr lonitrile type p y y carbon fibers are produced
using, as a raw material, polymers mainly containing
acrylonitrile. Practically, they are carbon fibers obtained
through a spinning process for spinning acrylonitrile type
fibers, oxidizing process for converting the fibers into
oxidized fibers by heating them at 200 to 400 C in air atmosphere,
and carbonizing process for heating and carbonizing the
resultant fibers at 300 to 2500 C in an inert gas such as
nitrogen, argon, helium, and the like,_and preferably used as
composite material-reinforcing fibers. Therefore, thefibers
have high strength as compared with other type carbon fibers
and can be formed into carbon fiber paper with high mechanical
strength.
Theznethodsapplicable forthe paper-manufacturing method
for producing the carbon fiber paper include a wet method for
producing paper by dispersing carbon short fibers in a liquid
medium and a dry method comprising steps of dispersing carbon
short fibers in air and depositing the fibers. Aproper amount
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CA 02485232 2001-01-25
of an organic high-molecular substance is preferable to be
added as a binder for binding the carbon fibers one another.
In that way, the strength of carbon fiber paper is maintained
and separation of the carbon fibers from carbon fiber paper
during the production process can be prevented and the
orientation of the carbon fibers can be prevented from
changing.
As the organic high-molecular compound, polyvinyl alcohol
or acrylonitrile type polymers in pulp-like state or their
short fibers are preferable. The pulp-like materials or short
fibers of the acrylonitrile type polymers are especially
preferable since their carbonized materials can function as
conductors. Further, since the polyvinyl alcohol is excellent
in the contacting in the paper-manufacturing process, it is
preferable as a binder to suppress the separation of the carbon
short fibers. Further, the polyvinyl alcohol is almost all
decomposed and volatilized in the carbonization process in the
final stage of producing the electrode substrate and forms
voids. Owing to the existence of the voids, the water and gas
permeability is improved and therefore, the polyvinyl alcohol
is preferable.
The pulp-like materials have a structure in which a large
.number of fibrils with several m or thinner diameter are
branched from fibrous trunks, and in a sheet-like material
produced from the pulp-like materials, the fibers are
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CA 02485232 2001-01-25
efficiently entangled with one another and even if a thin
sheet-like material, the material has an advantage that it is
excellent in the handling property. The short fibers of
acrylonitrile type polymers can be obtained by cutting fiber
threads made of acrylonitrile type polymers or tows of the
fibers in a prescribed length.
The content of the organic high-molecular compound in the
carbon fiber paper is preferably within a range from 5 to 40%
by mass and more preferably within a range from 15 to 30% by
mass. In order to lower the electric resistivity of the
electrode substrate obtained by impregnating the carbon fiber
paper with a resin and carbonizing the paper, it is better as
the content is less, and the content is preferably not higher
than 40% by mass. From the viewpoint of keeping the strength
and the shape of the carbon fiber paper, the content is
preferably 5% by mass or higher.
As a method for mixing the pulp-like materials or short
fibers of the organic high-molecular compound with carbon
fibers, the following methods are preferable: a method for
stirring and dispersing them together with carbon fibers in
water and a method for directly mixing them. In order to evenly
disperse them, the method for dispersing and diffusing in water
is preferable.
After the carbon fiber paper is produced, the paper is
hot-pressed by hot-press rolls to make the orientation and the
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CA 02485232 2001-01-25
thickness of the carbon fibers even and the fuzz which is
characteristic of the carbon fibers cari be suppressed to a
minimum. The heating temperature of the hot-press rolls is
preferably. 100 to 150 C and the pressure is preferably 0.5 to
20 MPa.
The porous carbon electrode substrate for a fuel cell of
the present invention is a porous carbon electrode substrate
for a fuel cell having the thickness of 0.05 to 0.5 mm, the
bulk density of 0.3 to 0.8 g/cm3, and the bending strength of
10 MPa or higher measured by a three-point bending test in
conditions of using a sample width of 1 cm, a strain rate of
10 mm/min, and a distance between supporting points of 2 cm,
and a deflection of 1.5 mm or more at the time of bending.
The porous carbon electrode substrate for a fuel cell
comprises carbonaceous materials such as carbon fibers as main
constituent elements and is a substrate having water or gas
permeability and conductivity sufficient to function as an,
electrode of a fuel cell. As the gas permeability of the porous
electrode substrate, it is preferable to be 200 ml-mm/hr-
cm -mmAq or higher. As the conductivity, the through-plane
resistivity is preferably 10 mS2-cm2 or lower in the case where
the resistivity value is measured by applying electric current
with current density of 10 mA/cm2 while the electrode substrate
being sandwiched between copper plates and pressurized at 1
MPa from the upper and the.lower sides of the copper plates.
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The thickness of the porous carbon electrode substrate
is needed to be 0.05 to 0.5 mm from the viewpoint of the
resistivity and preferable to be 0.1 to 0.3 mm. If the
thickness is thinner than 0. 05 mm, the strength in the thickness
direction becomes low and it is insufficient to stand handling
at the time of assembling a cell stack. On the other hand,
if exceeding 0.5 mm, the electric resistivity becomes high and
the total thickness becomes thick when a cell stack is assembled.
The bulk density is required to be 0.3 to 0.8 g/cm3 and
preferable to be 0.4 to 0.7 g/cm3. In the case where the bulk
density is lower than 0.3 g/cm3, not only the electric
resistivity is increased but also satisfactory flexibility
cannot be obtained. On the other hand, in the case where the
bulk density exceeds 0.8 g/cm3, the gas permeability is low
and the performance of a fuel cell is decreased.
The bending strength of the porous carbon electrode
substrate of the present invention is required to be 10 MPa
or higher, preferably 40 MPa or higher, in the case where it
is measured in conditions of using a sample width of 1 cm, a
strain rate of 10 mm/min, and a distance between supporting
points of 2 cm. If less than 10 MPa, the handling becomes
difficult and,. for example, the substrate easily cracks at the
time of being rolled around a roll. By controlling the bending
strength to be 10 MPa or higher, cracking can be prevented at
the time of bending the electrode substrate. Moreover, the
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CA 02485232 2001-01-25
deflection at the time of bending is 1.5 mm or more, preferably
2.0 mm or more. In the case where the bending deflection is
less than 1.5 mm, the electrode substrate is easy to be broken
at the time of being continuously rolled around a roll and it
becomes difficult to produce and handle a long electrode
substrate.
It is preferable for the porouscarbon electrode substrate
for fuel cells of the present invention to have length of 1
m or longer and be able to be rolled around a roll with the
outer diameter of 50 cm or smaller. If the electrode substrate
is long and able to be rolled around a roll, not only the
productivity of the electrode substrate is increased but also
production of MEA (membrane/electrode assembly) in a
successive process can continuously be carried out to
contribute to the considerable cost down of a fuel cell. For
that, the electrode substrate is preferable to be flexible
enough to be rolled around a roll with the outer diameter at
longest 50 cm, desirably 40 cm or smaller. The carbon electrode
substrate which is able to be rolled around a roll with the
outer diameter of 50 cm or smaller is excellent in flexibility
and in through-passing property in the MEA production process,
which is a successive process of the rolling, and therefore,
it is preferable. Further, if the electrode substrate can be
rolled around a roll with the outer diameter of 50 cm or smaller,
the carbon electrode substrate in the form of a product can
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CA 02485232 2001-01-25
be compact and is advantageous in the packing and
transportation cost. Also, in terms of prevention of breaking
the electrode substrate, the roll radius R(cm) is preferable
to satisfy the following inequality.
R > x' + 0.64 . . . (1)
0.8x
wherein x denotes the deflection quantity (cm) at the moment
of occurrence of rupture in bending in a three-point bending
test.
.In the present invention, carbon fiber paper containing
thin carbon fibers with an average diameter smaller than 5 m
and an average fiber length of 3 to 10 mm is impregnated with
a thermosetting resin, the thermosetting resin is cured by
heating and pressing, and then the'resultant carbon fiber paper
is carbonized to give the porous carbon electrode substrate
for a fuel cell.
The thermosetting resin to be employed for the present
inventiori is preferable a substance having adhesiveness
or fluidity at room temperature and also able to remain as a
conductive substance even after carbonization, and a phenol
resin, a furan resin and the like are applicable. A resol type
phenol resin obtained by a reaction of phenols and aldehydes
in the presence of an alkaline catalyst can be used as the
foregoing phenol resin. Further, a solid and thermally
fusible novolak type phenol resin produced by a reaction of
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CA 02485232 2001-01-25
phenols and aldehydes in the presence of an acidic catalyst
by a publicly known method may be dissolved and mixed in a resol
type fluid phenol resin, and in this case a preferable one is
a self-cross-linking type one containing a curing agent, for
example, hexamethylenediamine.
As the phenols, usable ones are, for example, phenol,
resorcin, cresol, xylol, and the like. As the aldehydes;
-
usable ones are, for example, formalin, paraformaldehyde,
furfural, and the like. Further, they may be used as mixtures.
Commercially available products as phenol resins may be used
for them.
The preferable ratio of the resin in the resin-impregnated
carbon fiber paper of the present invention is 30 to 70% by
mass. From the viewpoirit that the structure of the porous
carbon electrode substrate becomes dense and that the strength
of the electrode substrate to be obtained is high, 30% by mass
or higher is preferable. On the other hand, from the viewpoint
that the porosity and gas permeability of the electrode
substrate to be obtained can be kept excellent, 70% by mass
or lower is preferable. The term, resin-impregnated carbon
fiber paper, means carbon fiber paper impregnated with a resin
and not treated with heating and pressing yet, and in the case
where a solvent is used for impregnation with a resin, the term
means the one from which the solvent is removed.
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CA 02485232 2001-01-25
In the impregnation process of.a thermosetting resin, a
conductive substance may be mixed with the thermosetting resin.
As the conductive substance, examples are carbonaceous milled
fibers, carbon black, acetylene black, isotropic graphite
powder, and the like. The mixing ratio of the conductive
substance to be added in the resin is preferably 1 to 10% by,
mass based on the resin. If the mixing ratio is less than 1%
by mass, it is disadvantageous in that the effect on the
conductivity improvement is slight, and if the mixing ratio
exceeds 10% by mass, it is disadvantageous in that the effect
on the conductivity improvement tends to be saturated and that
cost is increased.
Preferable methods for impregnating carbon fiber paper
with a resin or a mixture of a resin and a conductor are a method
employing a squeezing apparatus and a method for overlaying
a thermosetting resin film on carbon fiber paper. The method
employing a squeezing apparatus is a method involving steps
of immersing carbon fiber paper in a resin solution or a resin
mixed solution, applying the solution to the whole body of the
carbon fiber paper evenly by the squeezing apparatus, and
adjusting the quantity of the solution by changing the distance
between rolls of the squeezing apparatus. In the case of a
relatively low viscosity, a spraying method or the like is also
applicable.
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The method of using a thermosetting resin film is a method
involving steps of once applying a thermosettin.g resin to mold
release paper to obtain a thermosetting.resin film and then
laminating the film to carbon fiber paper and carrying out
heating and pressing treatment to transfer the thermosetting
resin.
The heating and pressing process in the present invention
is preferable to be carried out continuously in the whole length
of the carbon fiber paper from the viewpoint of productivity.
Further, prior to the heating and pressing p`rocess, preheating
is preferably carried out. In the preheating process, the
thermosetting resin is softened and in the succeeding heating
and pressing process, the thickness of an electrode substrate
can be well controlled by pressing. An electrode substrate
with th~e desired-thickness and density can be obtained by
pressing the preheated resin-impregnated carbon fiber paper
at a temperature higher than the preheating temperature by 50 C
or more. In order to obtain an electrode substrate with the
desired thickness and density, a plurality of resin-
impregnated carbon fiber paper sheets may be piled and then
subjected to the heating and pressing treatment.
The foregoing heating and pressing treatment is
preferably carried out using a continuous type hot roll press
machine or a continuous type hot press machine equipped with
a pair of endless belts. The.latter continuous type hot press
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CA 02485232 2001-01-25
machine conveys a substrate by belts,and tensile force is
scarcely applied to the substrate. Consequently, the
substrate is hardly broken during the production and the
machine is excellent in terms of through-passing property. On
the other hand, the former continuous type hot roll press
machine is simple in the structure and its running cost is low.
The above described two heating and pressing manners are
suitable methods for continuously curing the resin and
preferable to be employed for production of the electrode
substrate of the present invention.
The pressing pressure at the time of employing the
foregoing continuous type press machine is preferably 1.5 x
10' to 1 x 105 N/m. The heating and pressing treatment is a
process necessary to sufficiently, penetrate fibers with the
resin and to increase the bending strength. By pressing at
the pressure of 1.5 x 104 N/m or higher when thermally curing
the resin, sufficient conductivity and flexibility can be
achieved. On the other hand, by pressing at the pressure of
1 x 10 N/m or lower, the vapor generated from the resin at
the time of curing the resin can sufficiently be released to
the outside and consequently occurrence of cracking can be
suppressed.
The heating temperature of the heating and pressing
treatment is preferably 140 C or higher from the viewpoint of
the hardening treatment duration and of the productivity and
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CA 02485232 2001-01-25
preferably 320 C or lower from the viewpoint of the cost for
the equipment such as heating and pressing apparatus.
Further preferably, the temperature is within a range of 160
to 300 C. The temperature of the foregoing preheating is
preferably within a range from 100 to 180 C.
In the present invention, it is preferable to continuously
carry out carbonization, which succeeds the resin curing, in
the whole length of the carbon fiber paper. If the electrode
substrate is long, not only the productivity of the electrode
substrate is increased, but also the succeeding process of MEA
production can continuously be carried out to contribute to
considerable cost down of a fuel cell. Practically, it is
preferable to carry out the carbonization by continuously
firing the whole length of the carbon fiber paper in a
temperature range of 1, 000 to 3, 000 C in an inert atmosphere.
In the carbonization of the present invention, pretreatment
by pre-carbonizing in an inert atmosphere of about 300 to 800 C
range may be carried out before the carbonization treatment
by firing in a temperature range of 1, 000 to 3, 000 C in an inert
atmosphere.
The electrode substrate finally obtained by the above
described manner is preferable to be rolled around a roll with
the outer diameter of 50 cm or smaller and more preferable to
be rolled_around a roll with the outer diameter of 40 cm or
smaller. If the electrode substrate can be rolled around a
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CA 02485232 2001-01-25
roll with the outer diameter of 50 cm or smaller, the electrode
.substrate in the form of a product can be compact and is
advantageous in the packing and.transportation cost.
Hereinafter, the present invention will more particularly
be described according to examples.
The physical values and.the like in the examples were
measured by the following methods.
1) Carbon fiber diameter
The diameter of carbon fibers was measured by helium-
neon laser (SLB DIA MEASURING SYSTEMV4 : produced by Anritsu Co.)
as described in JIS R-7601. The measurement was carried out
for 100 carbon fibers and 'an average value was employed as an
average diameter of the carbon fibers.
2) Thickness
The thickness was measured by employing a thickness
measurement apparatus, Dial Thickness Gauge 7321'Il`x (produced by
Mitsutoyo Co., Ltd. ). The size of the measuring gauge was 10
mm in diameter and the measurement pressure was constantly 1:5
kPa.
3) Bending strength of electrode substrate
The measurement was carried out by employing a bending
strength testing apparatus. The distance between the
supporting points was set to be 2 cm, load was applied at strain
- rate of 10 mm/min, and the rupture load of the pressing wedge
was measured from the starting the application of the load to
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CA 02485232 2001-01-25
the moment when samples were ruptured and the bending strength
was calculated according to the following equation.
Bending strength (MPa ) 2Wh2 ... (2)
wherein P: rupture load (N); L: distance between
supporting points (mm); W: width of a sample (mm) ; h: height
of a sample (mm).
Incidentally, the value in the longitudinal direction was
measured for continuous samples.
4) Deflection of electrode substrate
Measurement was carried out by employing a bending
strength testing apparatus. The distance between the
supporting points was set to be 2 cm, load was applied at strain
rate of 30 mm/min and the moving distance of the pressing wedge
was measured from the starting the application of the load to
the moment when samples were ruptured, to measure the
deflection.
5) Gas permeability coefficient
According to JIS-P8117 and using a Gurley densometer7'', the
-time taken for a gas in 200 mm3 volume to pass through was
measured to calculate the gas permeability coefficient.
6) Measurement of through-plane resistivity
The resistivity value was measured by applying electric
current with current density of 10 mA/cm- while a sample being
sandwiched between copper plates and pressurized at 1 MPa from
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CA 02485232 2001-01-25
the upper and the lower sides of the copper plates and the
piercing resistivit.y was calculated based on the following
equation.
Trough-plane resistivity (S1cm`) = measured resistivity
value (92) x sample surface area (cm2) ... (3)
Example 1
Fiber bundles of polyacrylonitrile tPAN) type carbon
fibers with an average fiber diameter of 4 m were cut to obtain
short fibers with an average fiber length of 3 mm.
Next, the short fiber bundles were spread in water and
sufficiently dispersed, then shortfibersof polyvinylalcohol
( PVA) (VBP 105-17m in cut length 3 mm; produced by Kuraray Co.,
Ltd..) as a binder was evenly* dispersed in 15% by mass in the.
total amount of the carbon fibers and PVA, paper manufacturing
was manually carried out according to JIS P-8209 method using
a standard square sheet machine (No. 2555 Standard square sheet
machine; produced by Kumagai Riki Industry Co., Ltd.), and the
obtained paper was dried to obtain carbon fiber paper_ PVA
fibers were in half-dissolved state and contacted the carbon
fibers with one another. The areal weight of the obtained
carbon fiber paper was 60 g/cm2.
The carbon fibe.r paper was immersed in an ethanol solution
containing 15% by mass of a phenol resin (Resitop PL-2211
produced by Gun-ei Chemical Industry Co., Ltd.) and pulled out
_ 23 -
CA 02485232 2001-01-25
to impregnate 100 parts by mass of the carbon fibers with 100
parts by mass of the phenol resin and then dried with a hot
air, and then the resultant carbon fiber paper was sandwiched
between fluorinated iron plates and kept in conditions of 170 C
and 15 MPa for 15 minutes by a batch press apparatus to cure
the phenol resin.
Successively, the obtained intermediate substrate was
heated at 2,000 C in a nitrogen gas atmosphere in a batch
carbonization furnace for one hour to carbonize the substrate
and obtain a porous carbon electrode substrate. Both of the
bending strength and the deflection were consequently
excellent.
The production conditions of carbon fiber paper sheets
of the examples and comparative examples are shown in Table
1: the production conditions of electrode substrates in Table
2: and the evaluation results of the electrode substrates in
Table 3.
Example 2
An electrode substrate was obtained in the same manner
as the example 1 except that the paper manufacturing was
continuously carried out in the following manner.
Fiber bundles of short carbon fibers were spread in water
in a slurry tank and sufficiently dispersed, and then short
fibers of polyvinyl alcohol (PVA) as a binder (the same one
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CA 02485232 2001-01-25
used in the example 1) was evenly dispersed and web was sent
out. The sent out web was passed through short net plate and
dried by a drier to obtain carbon fiber paper with the length
of 20 m. The obtained carbon fiber paper had the areal weight
of 60 g/cm2. Further the long carbon fiber paper was cut into
25 cm length for the successive processes.
The electrode substrate of the present invention was
provided with remarkably improved strength owing to the
continuous paper-manufacturing and was also excellent in the
deflection.
Example 3
A long carbon fiber paper sheet was produced in the same
manner as the example 2, and the carbon fiber paper was
impregnated with a thermosetting resin by a dip-nip method.
That is, the carbon fiber paper was continuously sent to a tray
containing a methanol solution containing of 20% by weight of
a phenol resin (Phenolite J-325 , produced by Dainippon Ink and
Chemicals, Inc.), the resin was squeezed by a squeezing
apparatus, and then a hot air was continuously blown to dry
and obtain resin-impregnated carbon fiber paper. In this case
100 parts by mass of carbon fibers were impregnated with 100
parts by mass of the phenol resin.
Next, the resin-impregnated carbon fiber paper was
continuously heated and pressed by a continuous type hot roll
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CA 02485232 2001-01-25
press machine illustrated in FIG. 1 to obtain resin-cured
carbon fiber paper. That is, the above described resin-
impregnated'carbon fiber paper 1 was sent out the rolls and
while being sandwiched between mold release agent-coated
substrates 2, the carbon fiber paper was sent to a preheating
zone 4, successively to a heating and pressing zone 5, and then
the mold releas.e agent-coated substrates 2 were removed and
the obtained resin-cured carbon fiber paper was rolled around
a roll. In this case, the preheating temperature in the
preheating zone was 150 C and the preheating duration was 5
minutes and the temperature of the heating and pressing zone
was 250 C and the press pressure was 1.5 x 104 N/m line pressure.
After that, the obtained resin-cured carbon fiber paper
with the width of 30 cm and the length of 20 m was cut at every
25 cm and fired in the same manner as the- examples 1 and 2 to
obtain an electrode substrate. Both of the bending strength
and the deflection were excellent.
Example 4
An electrode substrate was obtained in the same manner
as the example 3 except that the press pressure o.f the roll
press machine was heightened to 7.5 x 104 N/m of line pressure.
Owing to the high press pressure, the substrate was made thin
and the bending strength was hi.gh and the deflection value was
also high.
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CA 02485232 2001-01-25
Example 5
A.resin-cured carbon fiber paper obtained by paper-
manufacturing, impregnating with a resin, and subjecting to
roll press in the same manner as the example 4 was heated for
minutes in a continuous firing furnace at 2,O00 C in a
nitrogen gas atmosphere, without being cut into pieces, to
carbonize the carbon fi.ber.paper and to continuously obtain
}
a carbon electrode substrate with the length of 20 m, and the
10 substrate was rolled around a cylindrical paper tube with the
outer diameter of 30 cm, The thickness was thin, the bending
strength was high and the deflection value was also high.
Example 6
After being subjected to continuous paper-manufacturing
and impregnating with a resin process in the same manner as
the example 3 except that the areal weight was controlled to
be 100 g/m the obtained resin-impregnated carbon fiber paper
was continuously subjected to.hot press by a continuous type
hot press machine (a double belt press machine: DBP) equipped
with a pair of endless belts as illustrated in FIG. 2 to obtain
resin-cured carbon fiber paper. That is, the above described
resin- impregnated carbon fiber paper 1 was placed between the
mold release agent-coated substrates 2 and were sent between
continuos belt apparatuses 3a, 3b, to a preheating zone 4, and
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CA 02485232 2001-01-25
successively to a heating and pressing zone S. After that;
as same in the case of the roll press machine of FIG. 1, the
mold release agent-coated substrates 2 were removed and the
obtained resin-cured carbon fiber paper was rolled around a
roll. The continuous belt apparatuses 3a, 3b conveyed
resin-impregnated carbon fiber paper 1 and the like by
respectively being rotated. In this case, the preheating
temperature in the preheating zone was 160 C and the preheating
duration was 5 minutes and the temperature of the heating and
pressing zone was 280 C and the press pressure was 1.5 x 104
N/m of line pressure. After that, the obtained resin-cured
carbon fiber paper with the width of 30 cm and the length of
m was cut at every 25 cm and fired in the same manner as
the examples 1 and 2 to obtain an electrode substrate. The
15 substrate was smooth, and both of the bending strength and the
deflection were excellent.
Example 7
An electrode substrate was obtained in the same manner
20 as the example 6 except that the press pressure of the double
belt press (DBP) machine was increased to 7.5 x 104 N/m of line
pressure. Owing to the high press pressure, the sub.strate was
made thin and the bending strength was high and the deflection
value was also high.
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CA 02485232 2001-01-25
Example 8
Continuous paper-manufacturing and impregnation with a
resin were carried out in the same manner as the example 7 except
that carbon fiber paper was continuously obtained while the
areal weight being adjusted to be 30 g/m2. The heating and
pressing process was carried out in the same manner as the
example 7 except two sheets of the obtained resin-impregriated
carbon fiber paper were piled in the manner that the same
paper-manufactured faces were set face to face in the inside
at the time of double belt press. The obtained substrate,
without being cut, was subjected to precarbonization treatment
by heating.at 300 to 600 C for 5 minutes in a nitrogen gas
atmosphere in a furnace and then carbonized by heating at 1, 600
to 2, 000 C for 10 minutes in a continuous carbonizing furnace
to continuously obtain a carbon electrode substrate with the
length of 20 m, and-the substrate was rolled around a paper
tube with the outer diameter of 30 cm. The obtained substrate
was no.t at all warped and thin and provided with high bending
strength and a high deflection value as well.
Example 9
A carbon electrode substrate was obtained in the same
manner as the example 8 except that short fibers with an average
fiber diameter of 4 m and an average fiber length of 6 mm were
used instead of the short fibers with an average fiber diameter
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CA 02485232 2001-01-25
of 4~.tm and an average fiber length of 3 mm. Although the
dispersibility was relatively decreased, the strength, the
deflection and the gas permeability were all together
excellent.
S
Example 10
Fiber bundles of polyacrylonitrile (PAN) type carbon
fibers with an average fiber diameter of 4 m were cut to obtain
short fibers with an average fiber length of 3 mm. On the other
hand, fiber bundles of PAN type carbon fibers with an average
fiber diameter of 7 m were cut to obtain short fibers with
an average fiber length of 6 mm. Next, the short fiber bundles
so mixed in the ratio of the short fibers with the fiber diameter
of 4 m and with the fiber diameter of 7 m as 4 m/7 pm = 8/11
were spread in water and sufficiently dispersed, and then short
fibers of polyvinyl alcohol (PVA) (the same one used in the
example 1) as a binder was evenly dispersed in 5% by mass based
on.the total amount of the carbon fibers and PVA, and paper
manufacturing was carried out according to JIS P-8209 method
using a standard square sheet machine (the same one used in
the example 1). Except that described above, the obtained
paper was subjected to resin impregnation, batch press, and
batch carbonization to obtain an electrode substrate. Both
of the bending strength and the deflection were consequently
excellent.
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CA 02485232 2001-01-25
Example 11
Paper manufacturing was carried out by using a wet type
continuous paper-manufacturing apparatus, and impregnation
with a resin, batch press and batch carbonization were carried
out in the same manner as the example 2 except that the short
carbon fibers and PVA were mixed in the same ratio as that of
the example 10 to obtain an electrode substrate. As compared
with the results of the example 10, the bending strength was
remarkably increased and the deflection was also excellent.
Example 12
Paper manufacturing was carried out by using a wet type
continuous paper-manufacturing apparatus, and continuous
resin impregnation and resin drying, and then roll press and
batch carbonization were carried out in the same manner as the
example 3 except that the short carbon fibers and PVA were mixed
in the same ratio as that of the example 10 to obtain an electrode
substrate. Both of the bending strength and the deflection
were excellent.
Example 13
Paper manufacturing was carried otit by using a wet type
continuous paper-manufacturing apparatus, and continuous
resin impregnation and resin drying, and then roll press and
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CA 02485232 2001-01-25
batch carbonization were carried out in the same manner as the
example 4 except that the short carbon fibers and PVA were mixed
in the same ratio as that of the example 10 to obtain an electrode
substrate. Since pressing was carried out at a higher pressure
than that in the example 12, the electrode substrate was thinner
than the electrode substrate of the example 12, and bending
strength and the deflection were higher than those of the
substrate of the example 12.
Example 14
Paper manufacturing was carried out by using a wet type
continuous paper-manufacturing apparatus, and continuous
resin impregnation and resin drying, and then roll press and
continuous carbonizing were carried out in the same manner as
the example 5 except that the short carbon fibers and PVA were
mixed in the same ratio as that of the example 10 to obtain
an electrode substrate with the width of 30 cm and the length
of 20 m which was rolled on a cylindrical paper tube with the
outer diameter of 30 cm. The electrode substrate was thin and
the bending strength and the deflection of the substrate were
high.
Example 15
Paper manufacturing was carried out by using a wet type
continuous paper-manufacturing apparatus, and continuous
_ 32 _
CA 02485232 2001-01-25
resin impregnation and resin drying, and then double belt press
(DBP) and batch carbonization were carried out in the same
manner as the example 6 except that the short carbon fibers
and PVA'were mixed in the same ratio as that of the example
10 to obtain an electrode substrate. Both of the bending
strength and the deflection of the substrate were consequently
excellent.
Example 16
Paper manufacturing was carried out by using a wet type
continuous paper-manufacturing apparatus, and continuous
resin impregnation and resin drying, and double belt press
(DBP) and batch carbonization were carried out in the same
manner as the example 7 except that the short carbon fibers
and PVA were mixed in the same ratio as that of the example
10 to obtain an electrode substrate. Bince pressing was
carried out at a higher pressure than that in the example 15,
the electrode substrate was thinner than the electrode
substrate of the example 15 and bending strength and the
deflection were higher than those of the substrate of the
example 15.
Example 17
Paper manufacturing was carried out by using a wet type
continuous paper-manufacturing apparatus, and continuous
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CA 02485232 2001-01-25
resin impregnation and resin drying, and double belt press
(DBP) and continuous carbonizing were carried out in the same
manner as the example 8 except that the short carbon fibers
and PVA were mixed in the same ratio as that of the example
10 to obtain an electrode substrate with the width of 30 cm
and the length of 20 m which was rolled on a cylindrical paper
tube with the outer diameter of 30 cm. The obtained electrode
substrate was completely free of warp and thin and provided
with.a high bending strength and a high deflection value.
Example 18
A carbon electrode substrate was obtained in the same
manner as the example 17 except that short fibers with an
average fiber diameter of 4 m and an average fiber length of
6 mm were used instead of the short fibers with an average fiber
diameter of 4 m and an average fiber length of 3 mm. Although
the dispersibility was relatively decreased, the strength, the
deflection and the gas permeability were all together
excellent.
Example 19
A carbon electrode substrate was obtained in the same
manner as the example 1 except that polyacrylonitrile (PAN)
type pulp was used as a binder instead of PVA when paper
manufacturing. Although the bonding force of the short carbon
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CA 02485232 2001-01-25
fibers was lower than that in the case of using PVA, 'both of
the strength and the deflection were consequently excellent.
Example 20
A carbon electrode substrate was obtained in the same
manner as the example 1 except that carbon fiber paper was
impregnated with a phenol resin using a resin solution of the
phenol resin mixed with 1% by mass of carbon black MA 100 7m
(produced by Mitsubishi Chemical Industries Ltd.) versus the
resin, at the time of resin impregnation. The conductivity
was a high-value.
Example 21
A carbon electrode substrate was obtained in the same
manner as the example 8 except that 35 parts by mass of carbon
fiber paper was impregnated with 65 parts by mass of the phenol
resin. Although the gas permeability was slightly decreased,
both of the bending strength and the deflection were excellent.
Example 22
After a long carbon fiber paper sheet was continuously
obtained in the same manner as the example 2, long phenol resin
films with areal weight of 30 g/m~ were obtained by applying
a phenol resin (Phenolite .5900114, produced by Dainippon Ink and
Chemicals, Inc.) from which a solvent was removed to mold
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CA 02485232 2001-01-25
release paper sheets by a coater. The carbon fiber paper sheet
was sandwiched between the phenol resin films from the upper
and the lower sides to transfer the phenol resin to the carbon
fiber paper sheet, and then the carbon fiber paper sheet was
subjected to degassing and rolled.
The obtained resin-impregnated carbon fiber paper was
subjected to press curing by a double belt machine and
continuously carbonized in the same manner as the example 8
except that the obtained resin-impregnated carbon fiber paper
was not piled double, to obtain an electrode substrate with
the width of 30 cm and the length of 20 m. The gas permeability
was excellent and both of the bending strength and the
deflection were excellent as well.
Comparative example 1
Carbon fiber paper of 60 g/m` was obtained by continuous
paper manufacturing process in the same manner as the example
2 while using only PAN type short carbon fibers with an average
fiber diameter of .7 pm as carbon fibers (the same ones as used
in the example 10). Further, an electrode substrate was
produced from the carbon fibers by impregnation with resin in
the same manner as the example 3 and belt press and continuous
carbonization in the same manner as the example 22. Although
the gas permeability coefficient was high, the deflection was
- 36 -
CA 02485232 2001-01-25
low to cause cracking when the substrate was rolled around a
roll.
Comparative example 2
Carbon fiber paper of 30 g/mz was obtained by continuous
paper manufacturing process in the same manner as the example
8 while using only PAN type short carbon fibers with an average
fiber diameter of 7 pm as carbon fibers as same in the
comparative example 1. Successively, the carbon fiber paper
was subjected to impregnation with resin in the same manner*
as, the example 3, but without carrying out press, the resin
was continuously cured at 180 C and the carbon fiber paper was
continuously carbonized as it was. The obtained electrode
substrate was very brittle.
Comparative example 3
An electrode substrate was produced in the same manner
as the example 1 except that the pitch type carbon fibers with
an average fiber length of 11 mm were used instead of the PAN
type carbon fibers. The bending strength was inferior and the
electrode substrate was brittle.
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CA 02485232 2001-01-25
Table 1 Methods for producing carbon fiber paper sheets
in examples and comparative examples
A)CFof B)CFof
Fiber Fiber Areal
4 nt len ath of 7pin lenoth of Mixing weiglit of Paper-
diaineter dianieter manufac-
in the CF of 4 in the CF of 7 C) ratio by carbon
total CF ~ total CF ~ Binder mass fiber
o diameter o diameter A/B/C paper
(% by (~) (% by (mm) (glm2) method
niass) mass)
Example I l00 3 - - PVA 85/0/15 60 manual
Exaniple 2 100 3 - - PVA 85/0/15 60 continuous
Example 3 100' 3 - - PVA 85/0/15 60 continuous
Example 4 100 3 - - PVA 85/0/15 60 continuous
Example 5 100 3 - - PVA 85/0/15 60 continuous
Exaniple 6 100 3 - - PVA $510/15 100 continuous
Exaniple 7 100 3 - - PVA 85/0/15 100 continuous
Example. 8 100 3 - - PVA 85/0/15 30x2 continuous
Example 9 100 6 - - PVA 85/0/15 30x2 continuous
Example 10 42 3 58 6 PVA 40/55/5 60 manual
Example 11 42 3 58 6 PVA 40/55/5 60 continuotis
Example 12 42 3 58 6 PVA 40/55/5 60 continuous
Exaniple 13 42 3 58 6 PVA 40/55/5 60 continuous
Example 14 42 3 58 6 PVA 40155/5. 60 continuous
Example 15 42 3 58 6 PVA 40/55/5 100 continuous
Example 16 42 3 58 6 PVA 40/55/5 = 100 continuous
Exaniple 17 42 3 58 6 PVA 40/5515 30x2 continuous
Example 18 42 6 58 6 PVA 40/55/5 30x2 continuous
Example 19 100 3 - - p~P 85/0/15 60 manual
Example 20 l00 3 - - PVA 85/0/15 60 manual
Example 21 100 3 - - PVA 85/0115 30x2 continuous
E?:atuple 22 100 3 - - PVA 85/0/15 60 continuous
Comparative - - 100 6 FVA 0/85/15 60 continuotis
eyample 1
Contparative
example - 100 6 PVA 0/85/15 30 continuous
2 .
Contpaiative pitch 100 11 - - PVA 85/0/15, 60 manual
example 3.
CF: carbon fibers
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CA 02485232 2001-01-25
Table 2 Methods for producing electrode substrate
in examples and comparative examples
Continuous
T7iermo- R~u~ Heating and Batch pressing
CF pressing Conductive Carbonization
setting mass pressing line substance method Rolled
resin Me~~ pressure pressure
ratio ~'a) (x10 N/m)
Etample I PL221 1 50/50 batch 15 - - batch
E\auple 2 PL2211 50/50 batch 15 - batch -
Exaniple 3 PJ325 50/50 roll - 1.5 - batch
Example 4 PJ325 50/50 roll - 7.5 - batch -
Example 5 PJ325 50/50 roll - 7.5 - continuous 20 m
Exantple 6 PJ325 50/50 DBP - 1.5 - batch
Example 7 PJ325 50/50 DBP - 7.5 - batch -
Example 8 PJ325 50/50 DBP - 7.5 - continuous 20 m
Example 9 PJ325 50/50 DBP - 7.5 - continuous 20 m
Exatnple 10 PL2211 50/50 batch 15 - - batch -
Example I 1 PL2211 50/50 batch 15 - - batch -
Example 12 PJ325 50/50 roll - 1.5 - batch -
Example 13 PJ325 50/50 roll - 7.5 - batch -
Example 14 PJ325 50/50 roll - 7.5 - continuous 20 m
Example 15 PJ325 50/50 DBP - 1.5 - batch -
Example 16 P.1325 50/50 DBP - 7.5 - batch -
Example 17 PJ325 50/50 DBP - 7.5 - continuous 20 m
Eaaniple 18 PJ325 50/50 DBP - 7.5 - continuous 20 m
Exaniple 19 PL2211 50/50 batch 15 - - batch -
Example 20~ PL2211 50/50 batch 15 - CB 1% batch -
Example 21 PJ325 65/35 DBP - 7.5 - continuous 20 m
Example 22 film 50/50 DBP - 7.5 - continuous 20 m
Comparative PJ325 50/50 DBP - 7.5 - continuous 20 m
etaniple 1
Comparative PJ325 50/50 - - - - continuous 20 m
example 2
Comparative PL2211 50/50 batch 15 - - batch -
example 3
CB: carbon black
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CA 02485232 2001-01-25
Table 3 Evaluation results of electrode substrates of
examples and comparative.examples
Bulk gead Trough-plane Gas
Thickness densi stren~ Deflection resistivity when permeability
(r'"") (g/cm ) (MPa~ (n'n') pressed at Z (mUhr/cm2/
I MPa (mS2-cm ) mmAq)
Exaniple 1 0:17 0.39 11 2.4 3.98 2880
Example 2 0.17 0.48 60 2.4 3.98 1020
Example 3 0.17 0.45 50 2.1 3.75 1780
Example 4 0.15 0.55 60 2.5 3,66 820
Example 5 0.14 0.57 80 2.7 3.22 760
Example 6 0.27 0.49 55 1.6 6.07 500
Example 7 0.23 0.58 78 1.8 5.89 440
Example 8 0.14 0,61 130 2.9 3.12 720
Example 9 0.14 0.58 92 2.7 3.11 1000
Example 10 0.16 0.39 13 2.3 4.08 1760
E-xanple 11 0.17 0.48 63 2.5 3.78 1400
Example 12 0.17 0.45 52 2.0 3.9 1460
Example 13 0.14 0.55 61 2.4 3.82 1000
Example 14 0.14 0.57 83 2.7 3.49 960
Example 15 0.27 0.49 . 57 1.5 6.47 860
Example 16 0.23 0.58 79 1.7 6.19 560
Example 17 0.14 0.58 92 2.6 3.12 900
Example 18 0.14 0.58 82 2.8 3.42 2400
Example 19 0.17 0.41 11 2.3 3.21 2800
Example 20 0.18 0.41 15 2.8 2.95 2600
Example 21 0.18 0.63 61 2.0 5.05 350
Example 22 0.18 0.55 82 2.0 4.23 370
Comparative 0.14 0.55 80 1.2 3.61 1500
example I
Comparative ` 0.14 0.29 4.5 1.2 2.55 3300
example 2
Coniparative 0.18 0.34 8 2.4 3.21 6000
exaniple 3
* The distance between supporting points was kept constantly at 2 cm.
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CA 02485232 2001-01-25
INDUSTRIAL APPLICABILITY
A porous carbon electrode substrate for a fuel cell of
the present invention is a substrate excellent in flexibility,
durable to bending and able to be rolled around a roll, and
thus having high productivity. Carbon fiber paper of the
present invention is suitable for producing such an excellent
electrode substrate. According to the production method of
the present invention for producing the porous carbon electrode
substrate for a fuel cell, such an excellent electrode
substrate can be produced.
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