U.S. patent application number 12/662160 was filed with the patent office on 2010-07-29 for crosslinked aromatic polymer electrolyte membrane.
This patent application is currently assigned to JAPAN ATOMIC ENERGY AGENCY. Invention is credited to Masaharu Asano, Jinhua Chen, Yasunari Maekawa, Masaru Yoshida.
Application Number | 20100190875 12/662160 |
Document ID | / |
Family ID | 39597792 |
Filed Date | 2010-07-29 |
United States Patent
Application |
20100190875 |
Kind Code |
A1 |
Chen; Jinhua ; et
al. |
July 29, 2010 |
Crosslinked aromatic polymer electrolyte membrane
Abstract
An aromatic polymer film substrate, or a grafted aromatic
polymer film substrate having a monomer introduced therein as graft
chains is irradiated with ionizing radiation to impart a
crosslinked structure. The aromatic polymer film substrate or the
grafted aromatic polymer film substrate, provided with the
crosslinked structure, is directly sulfonated to obtain a
crosslinked aromatic polymer electrolyte membrane. The crosslinked
aromatic polymer electrolyte membrane has low water uptake, high
proton conductivity, low methanol permeability, high chemical
stability, and excellent mechanical characteristics.
Inventors: |
Chen; Jinhua; (Takasaki-shi,
JP) ; Maekawa; Yasunari; (Takasaki-shi, JP) ;
Asano; Masaharu; (Takasaki-shi, JP) ; Yoshida;
Masaru; (Takasaki-shi, JP) |
Correspondence
Address: |
STAAS & HALSEY LLP
SUITE 700, 1201 NEW YORK AVENUE, N.W.
WASHINGTON
DC
20005
US
|
Assignee: |
JAPAN ATOMIC ENERGY AGENCY
Ibaraki
JP
|
Family ID: |
39597792 |
Appl. No.: |
12/662160 |
Filed: |
April 1, 2010 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
12068036 |
Jan 31, 2008 |
7714027 |
|
|
12662160 |
|
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Current U.S.
Class: |
521/27 |
Current CPC
Class: |
H01M 8/1011 20130101;
H01M 8/103 20130101; H01M 8/04197 20160201; Y02E 60/50 20130101;
H01M 8/1032 20130101; H01M 8/1088 20130101; H01M 8/1027 20130101;
H01M 8/1025 20130101; H01M 8/1018 20130101; Y02E 60/523 20130101;
Y02P 70/50 20151101; H01M 8/0289 20130101; Y02P 70/56 20151101 |
Class at
Publication: |
521/27 |
International
Class: |
B01J 41/12 20060101
B01J041/12 |
Foreign Application Data
Date |
Code |
Application Number |
Feb 8, 2007 |
JP |
29223/2007 |
Claims
1. A crosslinked aromatic polymer electrolyte membrane comprising:
an aromatic polymer film substrate having a crosslinked structure
imparted thereto, the aromatic polymer film substrate having
sulfonic acid groups introduced into aromatic rings thereof, and
the aromatic polymer film substrate comprises any of polyether
ether ketone, polyether imide, polyethylene naphtahlate, and liquid
crystal polymer (LCP), or a composite containing any of them.
2. The crosslinked aromatic polymer electrolyte membrane according
to claim 1, wherein the aromatic polymer film substrate is a
homopolymer, or has a structure having a monomer grafted to the
polymer.
3. The crosslinked aromatic polymer electrolyte membrane according
to claim 2, wherein the monomer is at least one monomer selected
from the group consisting of aromatic vinyl compounds, acrylic acid
and derivatives thereof, acrylamides, vinylketones, acrylonitriles,
vinyl fluoride-based compounds, and multifunctional monomers.
4. The crosslinked aromatic polymer electrolyte membrane according
to claim 1, wherein the crosslinked structure is a
multiple-crosslinked structure.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 12/068,036, filed Jan. 31, 2008, allowed. This application is
based upon and claims the priority of Japanese application no.
2007-29223, filed Feb. 8, 2007, and U.S. patent application Ser.
No. 12/068,036, filed Jan. 31, 2008, the contents being
incorporated herein by reference.
BACKGROUND
[0002] 1. Field
[0003] This invention relates to a crosslinked aromatic polymer
electrolyte membrane which is suitable for use in a polymer
electrolyte fuel cell, and which has low water uptake, high proton
conductivity, low methanol permeability, high chemical stability,
and excellent mechanical characteristics; and a method for
producing the crosslinked aromatic polymer electrolyte
membrane.
[0004] 2. Description of the Related Art
[0005] A fuel cell using a polymer electrolyte membrane is operated
at a temperature of as low as 150.degree. C., and has a high power
efficiency and a high energy density. Thus, such a fuel cell is
expected to serve as a power source for mobile instruments, a power
source for cogeneration stationary systems, or a power source for
fuel cell vehicles (automobiles), which utilizes methanol, hydrogen
or the like as a fuel.
[0006] In connection with the fuel cell, important component
technologies on polymer electrolyte membranes, electrocatalysts,
gas-diffusion electrodes, and membrane-electrode assemblies are
existent. Development of a polymer electrolyte membrane having
excellent characteristics for use in the fuel cell is one of the
most important technologies.
[0007] In the polymer electrolyte fuel cell, the polymer
electrolyte membrane acts as an "electrolyte" for conducting
hydrogen ions (protons), and also acts as a "separator" for
preventing direct mixing of hydrogen or methanol, as a fuel, with
oxygen. The polymer electrolyte membrane is required to have high
proton conductivity; excellent chemical stability ensuring
long-term durability, especially, resistance to hydroxide radicals
becoming a main cause of membrane deterioration (i.e., chemical
stability); long-term thermal durability at the operating
temperature of the cell, or at even higher temperatures; and
constant and high water retention properties of the membrane for
keeping proton conductivity high. To play the role of the
separator, the polymer electrolyte membrane is required to be
excellent in the mechanical strength and dimensional stability, and
to have low permeability to hydrogen, methanol and oxygen.
[0008] A perfluorosulfonic polymer electrolyte membrane "Nafion
(registered trademark of DuPont)" developed by DuPont, for example,
has generally been used as the electrolyte membrane for the polymer
electrolyte fuel cell. Perfluorinated polymer electrolyte membranes
of the related art, such as Nafion, are excellent in chemical
durability and stability. However, their water retention properties
are insufficient at high temperatures and low humidity. Thus, the
drying of the ion exchange membranes occurs, resulting in decreased
proton conductivity. They are also disadvantageous in that when
methanol is used as a fuel, swelling of the membrane or crossover
of methanol takes place.
[0009] They have also been defective in that their mechanical
characteristics under operating conditions involving temperatures
exceeding 100.degree. C., required for an automobile power source,
markedly decline. Furthermore, the production of the perfluorinated
polymer electrolyte membranes starts with the synthesis of
fluorine-based monomers. Thus, the manufacturing process is so
complex that a high cost is entailed. These have been a great
impediment to the commercialization of these polymer electrolyte
membranes-based fuel cells as power sources for stationary
cogeneration systems or power sources for fuel cell vehicles.
[0010] Under these circumstances, the development of a low-cost
polymer electrolyte membrane replacing the perfluorinated polymer
electrolyte membrane has been energetically carried out. For
example, attempts have been made to prepare partially fluorinated
polymer electrolyte membranes by introducing styrene monomers into
fluoropolymer films, such as polytetrafluoroethylene (PTFE),
poly(vinylidene fluoride) (PVDF), and ethylene-tetrafluoroethylene
copolymer (ETFE), by graft polymerization, and then sulfonating the
graft polymers (see, for example, JP-A-2001-348439 and
JP-A-2004-246376).
[0011] However, the fluoropolymer films have a low glass transition
temperature, so that their mechanical strength at high temperatures
of 100.degree. C. or higher considerably declines. When a high
electric current is flowed through the electrolyte membrane for a
long time, moreover, the sulfonic acid groups introduced into the
polystyrene graft chains become detached, resulting in the marked
lowering of the proton conductivity of the electrolyte membrane.
There is also the defect that crossover of hydrogen, as the fuel,
or oxygen occurs.
[0012] On the other hand, an aromatic polymer electrolyte membrane
has been proposed as a low-cost hydrocarbon-based polymer
electrolyte membrane (see, for example, U.S. Pat. No. 5,403,675).
Since the aromatic polymer electrolyte membrane has excellent
mechanical strength at high temperatures and low fuel permeability
to methanol, hydrogen, oxygen or the like, its use at high
temperatures is expected.
[0013] The aromatic polymer electrolyte membrane is prepared by
dissolving an aromatic polymer material, typified by an engineering
plastic, in a sulfonating solution such as concentrated sulfuric
acid or chlorosulfonic acid to sulfonate the aromatic polymer, and
then forming a solution of the sulfonated aromatic polymer into a
membrane by casting (see, for example, JP-T-11-502245 and
JP-A-06-049202).
[0014] The aromatic polymer electrolyte membrane is also obtained
by the polymerization of an aromatic monomer having sulfonic acid
groups bound thereto, and then forming the resulting polymer into a
membrane (See, for example, JP-A-2004-288497, JP-A-2004-346163, and
JP-A-2006-12791).
[0015] The aromatic polymer electrolyte membrane has excellent
characteristics at high temperatures, so that its use at high
temperatures is expected. However, the methods for preparing the
aromatic polymer electrolyte membranes disclosed in JP-T-11-502245,
JP-A-06-049202, JP-A-2004-288497, JP-A-2004-346163, and
JP-A-2006-12791 use large amounts of strong acids for the purpose
of dissolving the aromatic polymer materials, and thus use large
amounts of diluting water in order to precipitate the sulfonated
materials. As noted here, these methods require complicated steps.
Moreover, the membrane-forming process by casting needs large
amounts of organic solvents.
[0016] The electrolyte membranes prepared as above have no
crosslinked structure. If the degree of sulfonation is high, or the
temperature is heightened, therefore, problems occur, such as
dissolution in water, or considerable dimensional changes or marked
decreases in strength, due to absorption of water. As noted here,
the electrolyte membranes do not possess mechanical strength which
enables the shape of the electrolyte membrane to be maintained
under the cell operating conditions.
[0017] Furthermore, the sulfonic acid groups exist randomly in the
aromatic polymer chains, thus resulting in unclear separation
between a hydrophobic layer for maintaining mechanical strength and
an electrolyte layer in charge of proton conduction. Hence, proton
conductivity, fuel impermeability, and chemical stability are
insufficient.
[0018] The present invention has been accomplished in the light of
the above-described problems. It is an object of the invention to
provide an aromatic polymer electrolyte membrane which does not
cause a problem, such as dissolution in water, or a considerable
dimensional change or a marked decrease in strength, due to
absorption of water, which possesses mechanical strength enabling
the shape of the electrolyte membrane to be maintained under the
cell operating conditions, and which is sufficient in proton
conductivity, fuel impermeability, and chemical stability.
[0019] It is another object of the invention to provide a method
for producing the aromatic polymer electrolyte membrane, which does
not need complicated steps, can markedly reduce the cost of
production, and obviates the need for a membrane-forming step by
casting.
SUMMARY
[0020] A first aspect of the present invention is a crosslinked
aromatic polymer electrolyte membrane comprising an aromatic
polymer film substrate having a crosslinked structure imparted
thereto, the aromatic polymer film substrate having sulfonic acid
groups introduced into aromatic rings thereof.
[0021] The aromatic polymer film substrate can be a homopolymer, or
can have a structure having a monomer grafted to the polymer.
[0022] The monomer can be at least one monomer selected from the
group consisting of aromatic vinyl compounds such as styrene,
acrylic acid and its derivatives, acrylamides, vinylketones,
acrylonitriles, vinyl fluoride-based compounds, and multifunctional
monomers.
[0023] The aromatic polymer film substrate can be any of polyether
ketones, polyimides, polysulfones, polyesters, polycarbonates,
polyphenylene sulfides, and polybenzimidazoles, or a composite
containing any of these polymers.
[0024] A multiple-crosslinked structure can be possessed as the
crosslinked structure.
[0025] A second aspect of the present invention is a method for
producing a crosslinked aromatic polymer electrolyte membrane,
which comprises irradiating an aromatic polymer film substrate with
ionizing radiation to impart a crosslinked structure to the
aromatic polymer film substrate, and then sulfonating the
crosslinked aromatic polymer film substrate to produce a
crosslinked aromatic polymer electrolyte membrane having sulfonic
acid groups introduced into aromatic rings of the crosslinked
aromatic polymer film substrate.
[0026] The crosslinked aromatic polymer electrolyte membrane is
heat-treated, whereby a multiple-crosslinked structure can be
imparted to the crosslinked aromatic polymer electrolyte
membrane.
[0027] The crosslinked aromatic polymer electrolyte membrane of the
present invention has low water uptake, high proton conductivity,
low methanol permeability, high chemical stability, and excellent
mechanical characteristics. Thus, it can be expected to provide a
polymer electrolyte membrane optimal for a fuel cell for mobile
instruments, a fuel cell for stationary cogeneration systems, or a
fuel cell for automobiles, which utilizes methanol, hydrogen or the
like as a fuel. The polymer electrolyte membrane is suitable,
particularly, for use in a fuel cell for stationary cogeneration
system, which is desired to have a long-term durability, or a fuel
cell for automobiles which withstands use at high temperatures of
100.degree. C. or higher.
[0028] According to the method for producing the crosslinked
aromatic polymer electrolyte membrane of the present invention, a
highly crosslinked structure is imparted beforehand to the aromatic
polymer film substrate, or the monomer-grafted aromatic polymer
film substrate. Thus, the film substrate can be sulfonated directly
in the sulfonating solution. Compared with the methods of the
related art including the complicated waste acid treating and
membrane-forming steps, therefore, the cost of manufacturing can be
markedly reduced. Moreover, the microphase-separated structure of
the polymer electrolyte membrane can be designed by selecting the
film substrate within a wide range, controlling the degree of
sulfonating, or controlling the degree of grafting.
DESCRIPTION OF EMBODIMENTS
[0029] The crosslinked aromatic polymer electrolyte membrane of the
present invention can be prepared, for example, by introducing a
crosslinked structure into an aromatic polymer film substrate, or
the film substrate having a monomer graft-polymerized therewith, by
irradiation with ionizing radiation, and then introducing sulfonic
acid groups into aromatic rings of the aromatic polymer chains
and/or graft chains of the crosslinked film substrate directly by a
sulfonation reaction. Details of this preparation will be described
in detail below.
Aromatic Polymer Film Substrate:
[0030] The aromatic polymer film substrate usable in the present
invention may be any film, without restriction, as long as it is an
aromatic polymer film crosslinkable by means of ionizing radiation
(for example, a film of any of polyether ketones, polyimides,
polysulfones, polyesters, polyamides, polycarbonates, polyphenylene
sulfides, and polybenzimidazoles), a composite film containing any
of these aromatic polymers, or a graft film having a monomer
grafted to any of the aromatic polymers. The aromatic polymer film
substrate can be converted into a polymer electrolyte membrane
having proton conductivity by introducing proton-conducting
sulfonic acid groups by the sulfonation reaction of aromatic rings
contained in the aromatic polymer film substrate.
[0031] Polyether ether ketone is preferred as an example of the
polyether ketones, since it is capable of monomer graft
polymerization and crosslinking by ionizing radiation (or ionizing
radiation crosslinking), and the resulting crosslinked aromatic
polymer electrolyte membrane has low water uptake, high proton
conductivity, low methanol permeability, high chemical stability,
and excellent mechanical characteristics.
[0032] Polyether imide is preferred as an example of the
polyimides, since it is capable of monomer graft polymerization and
ionizing radiation crosslinking, and the resulting crosslinked
aromatic polymer electrolyte membrane has low water uptake, high
proton conductivity, low methanol permeability, high chemical
stability, and excellent mechanical characteristics.
[0033] Polysulfone is preferred as an example of the polysulfones,
since it is capable of monomer graft polymerization and ionizing
radiation crosslinking, and the resulting crosslinked aromatic
polymer electrolyte membrane has low water uptake, high proton
conductivity, low methanol permeability, high chemical stability,
and excellent mechanical characteristics.
[0034] Polyethylene naphthalate or liquid crystal polymer (LCP) is
preferred as an example of the polyesters, since these polymers are
each capable of monomer graft polymerization and ionizing radiation
crosslinking, and the resulting crosslinked aromatic polymer
electrolyte membrane has low water uptake, high proton
conductivity, low methanol permeability, high chemical stability,
and excellent mechanical characteristics.
Ionizing Radiation Crosslinking:
[0035] The term "ionizing radiation crosslinking", as used herein,
refers to introducing a crosslink between the aromatic polymer
chains, between the aromatic polymer chain and the grafted
molecular chain, or between the grafted molecular chains, of the
aromatic polymer film substrate, by irradiation with ionizing
radiation. By imparting the crosslinked structure, the aromatic
polymer film substrate is insolubilized in most solutions,
including sulfonating solutions, and organic solvents. As a result,
sulfonation reaction can be performed, with the shape of the
aromatic polymer film substrate being retained. Thus, the aromatic
polymer film substrate can be directly transformed into the
electrolyte membrane. Furthermore, the aromatic polymer electrolyte
membrane provided with the crosslinked structure has its water
containing properties suppressed markedly, thus exhibiting high
chemical stability and excellent mechanical strength which are
required of a polymer electrolyte membrane for a fuel cell.
[0036] The impartation of the crosslinked structure to the aromatic
polymer film substrate or the monomer-grafted aromatic polymer film
substrate is carried out by utilizing reaction between active
sites, such as radicals, generated on the aromatic polymer chains
by ionizing radiation. Thus, the ionizing radiation is not limited
to a particular radiation, as long as it is an energy source which
causes the reaction for generating activated species, such as
radicals, on the polymer chains. Examples of the ionizing radiation
are gamma rays, electron-beams, an ion beam, and X-rays.
[0037] The ionizing radiation is thrown onto the aromatic polymer
film substrate or the monomer-grafted aromatic polymer film
substrate at an absorbed dose of 0.5 to 200 MGy at room temperature
to 350.degree. C. under vacuum, under an inert gas or in the
presence of oxygen. By so doing, the crosslinked structure is
imparted. As a yardstick of the crosslinking density, the gel
percent of the aromatic polymer is named. The gel percent is
defined as the proportion, to the total weight, of the insolubles
weight of the polymer in a good solvent for the aromatic
polymer.
[0038] In the present invention, if the gel percent reaches 50% or
higher, the shape of the aromatic polymer film substrate can be
retained during the sulfonation reaction, and a crosslinked
aromatic polymer electrolyte membrane insoluble in water or an
organic solution is obtained. The necessary crosslinking radiation
dose varies with the type of the aromatic polymer film substrate.
In the case of a polyether ether ketone film substrate, for
example, less than 40 MGy is not sufficient to reach a gel percent
of 50%. Thus, the mechanical strength of the resulting crosslinked
aromatic polymer electrolyte membrane is so low that the
electrolyte membrane is difficult to use as an electrolyte membrane
for a fuel cell. A value of more than 100 MGy results in the
embrittlement of the resulting electrolyte membrane. With the
polyether ether ketone, therefore, irradiation at a crosslinking
radiation dose of 40 to 100 MGy is preferred.
[0039] Radicals generated in the presence of oxygen partially
become a peroxide structure. Thus, it is more preferred for the
irradiation atmosphere to be under vacuum or in an inert gas.
Irradiation at a high temperature can accelerate the crosslinking
by ionizing radiation, so that a high gel percent can be achieved
with a lower radiation dose. By heat-treating the irradiated sample
at 80.degree. C. or higher, the residual radicals are bound
together, and the crosslinking effect is enhanced. Hence, heat
treatment lasting 2 to 24 hours at 80 to 250.degree. C. under
vacuum is even more preferred.
Graft-Polymerized Monomer:
[0040] In the present invention, the monomer graft-polymerized with
the aromatic polymer film substrate includes, for example, aromatic
vinyl compounds such as styrene, acrylic acid and its derivatives,
acrylamides, vinylketones, acrylonitriles, vinyl fluoride-based
compounds, or multifunctional monomers. This is because graft
chains can be sulfonated in the resulting grafted aromatic polymer
film, and the graft chains can be crosslinked to each other by
irradiation with ionizing radiation.
[0041] The aromatic vinyl compounds such as styrene can be
represented by the following general formula (A):
##STR00001##
[0042] where X represents --H, --CH.sub.3, --CH.sub.2CH.sub.3,
--OH, --Cl, --F, --Br or --I, and Y represents --H, --CH.sub.3,
--CH.sub.2CH.sub.3, --CH.sub.2CH.sub.2CH.sub.3,
--C(CH.sub.3).sub.3, --OCH.sub.3, --OCH.sub.2CH.sub.3,
--OCH.sub.2CH.sub.2CH.sub.3, --OC(CH.sub.3).sub.3, --CH.sub.2Cl,
--CN, --SO.sub.3CH.sub.3, --Si(OCH.sub.3).sub.3, --Si
(OCH.sub.2CH.sub.3).sub.3, --CH.dbd.CH.sub.2, --OCH.dbd.CH.sub.2,
--C.ident.CH, --OH, --Cl, --F, or --Br.
[0043] The acrylic acid and its derivatives can be represented by
the following general formula (B):
##STR00002##
[0044] where X represents --H, --CH.sub.3, --CH.sub.2CH.sub.3,
--OH, --Cl, --F, --Br or --I, and Y represents --H, --CH.sub.3,
--CH.sub.2CH.sub.3, --CH.sub.2CH.sub.2CH.sub.3,
--C(CH.sub.3).sub.3, CH.sub.2Cl, --Si (OCH.sub.3).sub.3,
--Si(OCH.sub.2CH.sub.3).sub.3, or a benzene ring.
[0045] The acrylamides can be represented by the following general
formula (C):
##STR00003##
[0046] where X represents --H, --CH.sub.3, --CH.sub.2CH.sub.3,
--OH, --Cl, --F, --Br or --I, and Y represents --H, --CH.sub.3,
--CH.sub.2CH.sub.3, --CH.sub.2CH.sub.2CH.sub.3,
--C(CH.sub.3).sub.3, --CH.sub.2Cl, or a benzene ring.
[0047] The vinylketones can be represented by the following general
formula (D):
##STR00004##
[0048] where X represents --H, --CH.sub.3, --CH.sub.2CH.sub.3,
--OH, --Cl, --F, --Br, or --I, and n denotes an integer of 1 to
5.
[0049] Examples of the nitriles are acrylonitrile
(CH.sub.2.dbd.CHCN) and methacrylonitrile
[CH.sub.2.dbd.C(CH.sub.3)CN].
[0050] Examples of the vinyl fluoride-based compounds are
CF.sub.2.dbd.CF--C.sub.6H.sub.5,
CF.sub.2.dbd.CF--O--(CF.sub.2).sub.n--SO.sub.2F,
CF.sub.2.dbd.CF--O--CF.sub.2--CF
(CF.sub.3)--O--(CF.sub.2).sub.n--SO.sub.2F,
CF.sub.2.dbd.CF--SO.sub.2F,
CF.sub.2.dbd.CF--O--(CH.sub.2).sub.n--X, CH.sub.2.dbd.CH--O--
(CF)--X, CF.sub.2.dbd.CF--O--(CF.sub.2).sub.n--X,
CF.sub.2.dbd.CF--O--CF.sub.2--CF
(CF.sub.3)--O--(CF.sub.2).sub.n--X,
CF.sub.2.dbd.CF--O--(CH.sub.2).sub.n--CH.sub.3,
CH.sub.2.dbd.CH--O--(CF.sub.2).sub.n--CF.sub.3,
CF.sub.2.dbd.CF--O--(CF.sub.2).sub.n--CF.sub.3, and
CF.sub.2.dbd.CF--O--CF.sub.2--CF (CF.sub.3)--O--
(CF.sub.2).sub.n--CF.sub.3. (In these formulas, n denotes an
integer of 1 to 5, and X represents a halogen atom, specifically,
chlorine or fluorine.)
[0051] The multifunctional monomers are not limited, as long as
they have a structure which can impart a crosslink to graft chains
in a graft reaction. Examples of the multifunctional monomers are
bis(vinylphenyl)ethane, divinylbenzene,
2,4,6-triallyloxy-1,3,5-triazine (i.e., triallyl cyanurate),
triallyl-1,2,4-benzenetricarboxylate (i.e., triallyl trimellitate),
diallyl ether, bis(vinylphenyl)methane, divinyl ether,
1,5-hexadiene, and butadiene. By graft-polymerizing the
multifunctional monomer, a crosslinked structure can be imparted
between graft chains. The multifunctional monomer is preferably
used in a proportion by weight of 10% or less in all the monomers.
If more than 10% of the multifunctional monomer is used, the
resulting polymer electrolyte membrane becomes brittle.
Graft Polymerization:
[0052] In the present invention, graft polymerization of the
monomer with the aromatic polymer film substrate is performed by
utilizing graft active sites, such as radicals generated in the
aromatic polymer film substrate, by ionizing radiation. By
controlling the degree of grafting, a crosslinking effect in a
subsequent ionizing radiation crosslinking step, and a sulfonating
effect in a sulfonation step are provided. The degree of grafting
is preferably 0 to 200% by weight, more preferably 0 to 80% by
weight, based on the aromatic polymer film substrate. A degree of
grafting of more than 200% by weight results in the failure to
obtain the mechanical strength of the grafted aromatic polymer film
substrate suitable for a fuel cell.
Sulfonation Reaction:
[0053] In the present invention, the crosslinked structure is
imparted to the aromatic polymer film substrate, or the
monomer-grafted aromatic polymer film substrate, whereby the
aromatic polymer film substrate becomes insoluble in most
solutions, including a sulfonating solution, and organic solvents.
As a result, sulfonation reaction can take place, with the shape of
the aromatic polymer film substrate being retained. Consequently, a
crosslinked aromatic polymer electrolyte membrane having excellent
performance, which is directly applied to a fuel cell, can be
obtained from the aromatic polymer film substrate. Hence, it
becomes possible to use concentrated sulfuric acid, fuming sulfuric
acid, and halogen-based organic solutions of chlorosulfonic acid
(dichloroethane solution, chloroform solution, etc.) which have
been unusable, because the aromatic polymer film substrate, or the
monomer-grafted aromatic polymer film substrate, if without the
crosslinked structure, dissolves during the reaction.
Ion Exchange Capacity:
[0054] The polymer electrolyte membrane acts upon the proton
dissociation properties of the sulfonic acid groups introduced into
the film substrate by sulfonation. The amount of the sulfonic acid
groups is defined as the ion exchange capacity (unit: mmol/g) which
is the number of millimols of the sulfonic acid groups in 1 g of
the dry electrolyte membrane. The ion exchange capacity of the
polymer electrolyte membrane can be controlled according to the
sulfonation conditions (sulfonating reagent, type of the solvent,
sulfonation time, temperature) and the degree of grafting of the
grafted polymer membrane. To prepare a crosslinked aromatic polymer
electrolyte membrane having low water uptake and high proton
conductivity, the ion exchange capacity is preferably adjusted to
0.5 to 3.0 mmol/g. It is more preferably 0.8 to 1.6 mmol/g. At less
than 0.5 mmol/g, it is difficult to obtain practical proton
conductivity. If the ion exchange capacity exceeds 3.0 mmol/g,
however, high water uptake results, leading to a noticeable decline
in mechanical strength.
Multiple-Crosslinked Structure:
[0055] Upon heat treatment of the crosslinked aromatic polymer
electrolyte membrane after sulfonation, a further crosslinked
structure can be introduced onto the graft chain, thus resulting in
the enhancement of the mechanical strength and thermal stability.
For the efficient introduction of a heat-crosslinked structure
represented by the general formula (E) shown below, the heat
treatment is performed preferably for 0 to 24 hours at room
temperature to 300.degree. C. The thermal crosslinking reaction
proceeds efficiently within the range of the glass transition
temperature (Tg) of the aromatic polymer film substrate to
Tg+50.degree. C. Thus, the heat treatment conditions are more
preferably as follows: Under vacuum, 120 to 250.degree. C., 1 to 12
hours.
##STR00005##
Thickness of Polymer Electrolyte Membrane:
[0056] In the present invention, in order to lower the resistance
of the polymer electrolyte membrane for a fuel cell, it is
conceivable to thin the polymer electrolyte membrane. Under the
current circumstances, an excessively thin polymer electrolyte
membrane is easily broken, and the membrane itself is difficult to
produce. Thus, the crosslinked aromatic polymer electrolyte
membrane has a thickness of preferably 15 to 200 .mu.m, and more
preferably 20 to 100 .mu.m.
EXAMPLES
[0057] The present invention will now be described in detail by
Examples and Comparative Examples, which in no way limit the
invention.
[0058] The degree of grafting (%), ion exchange capacity (mmol/g),
water uptake (%), proton conductivity (S/cm), methanol permeability
(10.sup.-6 cm.sup.2/s), chemical stability (weight remaining rate),
and tensile strength (MPa) were evaluated as the characteristics of
each polymer electrolyte membrane. The measured values were
obtained by measurements described below. If the mechanical
strength of the resulting electrolyte membrane was too low to
prepare a sample for measurement, an evaluation "Not measurable"
was made.
(1) Degree of Grafting (%)
[0059] Let the polymer film substrate be a main chain portion, and
the portion graft-polymerized with the monomer be a graft chain
portion. Then, the weight ratio of the graft chain portion to the
main chain portion is expressed as a degree of grafting which
satisfies the following equation (Grafting (wt. %)):
Grafting=100.times.(Wg-Wo)/Wo [0060] Wo: Weight (g) in dry state
before grafting [0061] Wg: Weight (g) in dry state after grafting
(2) Ion Exchange Capacity (mmol/g)
[0062] The ion exchange capacity (IEC) of the polymer electrolyte
membrane is represented by the following equation:
IEC=n/Wm [0063] n: Amount (mmol/g) of sulfonic acid groups in
polymer electrolyte membrane [0064] Wm: Dry weight (g) of polymer
electrolyte membrane
[0065] The measurement of n was made by immersing the polymer
electrolyte membrane in a 1M sulfuric acid solution for 4 hours at
50.degree. C. to convert it into a proton type (H-type) completely,
then washing the polymer electrolyte membrane with deionized water
until pH=6 to 7, removing the free acid completely, then immersing
the polymer electrolyte membrane in a saturated aqueous solution of
NaCl for 24 hours to perform ion exchange, thereby liberating the
proton H.sup.+, and then acid-base titrating the electrolyte
membrane and its aqueous solution with 0.02M NaOH to determine the
amount of the sulfonic acid groups of the polymer electrolyte
membrane as the amount of protons H.sup.+, n=0.02 V (V: volume (ml)
of 0.02M NaOH used in the titration).
(3) Water Uptake (%)
[0066] At 80.degree. C., the H-type polymer electrolyte membrane
preserved for 24 hours in water was withdrawn. That is, water on
its surface was lightly wiped off, whereafter the wet weight Ww was
measured. This membrane was dried in a vacuum for 16 hours at
60.degree. C., and then measured for weight, whereby the dry weight
Wd of the polymer electrolyte membrane was determined. The water
uptake was calculated from the following equation based on Ww and
Wd:
Water uptake=100(Ww-Wd)/Wd
(4) Proton Conductivity (S/cm)
[0067] At room temperature, the H-type polymer electrolyte membrane
preserved in water was withdrawn. That is, the polymer electrolyte
membrane was sandwiched between platinum electrodes, and the
membrane resistance due to impedance was measured. The proton
conductivity of the polymer electrolyte membrane was calculated
using the following equation:
.kappa.=d/(RmS) [0068] .kappa.: Proton conductivity (S/cm) of
polymer electrolyte membrane [0069] d: Distance (cm) between
platinum electrodes [0070] Rm: Resistance (.OMEGA.) of polymer
electrolyte membrane [0071] S: Cross-sectional area (cm.sup.2) for
electric flow of polymer electrolyte membrane in measurement of
resistance
(5) Test for Evaluation of Methanol Permeability
[0072] The methanol permeability at 80.degree. C. was determined by
diffusion experiments using an H-type diffusion cell. The water
side of the cell was 100 mL in volume, and the methanol side of the
cell was charged with 100 mL of an aqueous solution of methanol
having a concentration of 10M. A permeation port of the H-type
cell, where the electrolyte membrane was interposed, was in a
circular form with a diameter of 2 cm. The system was stabilized at
80.degree. C. with stirring, and the methanol concentration was
measured at constant time intervals. The methanol permeability was
evaluated based on the results obtained.
P = V .times. d ( M MeOH - M H 2 O ) .times. S .times. M H 2 O t
##EQU00001## [0073] P: Methanol permeability coefficient
(cm.sup.2/s) of polymer electrolyte membrane [0074] V: Volume
(cm.sup.3) of water [0075] d: Thickness (cm) of polymer electrolyte
membrane [0076] M.sub.Me0H Concentration of methanol solution in
time t (seconds) [0077] M.sub.H2O: Methanol concentration in
aqueous solution in time t (seconds)
(6) Chemical Stability (Weight Remaining Rate, %)
[0078] The weight of the polymer electrolyte membrane after drying
under vacuum for 16 hours at 60.degree. C. was designated as
W.sub.3, and the dry weight of the electrolyte membrane after
immersion for 24 hours in a 3% solution of hydrogen peroxide at
80.degree. C. was designated as W.sub.4. The chemical stability was
determined by the following equation:
Chemical stability=100(W.sub.4/W.sub.3) (%)
(7) Mechanical Strength
[0079] The tensile strength (MPa), as the mechanical strength of
the polymer electrolyte membrane, was measured using a dumbbell
specimen in accordance with JIS K7127 at room temperature (about
25.degree. C.) and humidity RH of 50%.
Example 1
[0080] A 6 cm.times.20 cm polyether ether ketone (hereinafter
referred to as PEEK) film substrate (thickness 25 .mu.m) was fixed
to an irradiation stand. In this state, the PEEK film substrate was
irradiated with electron-beams (30 mA, voltage 1 MV) for 50 minutes
at a radiation dose of 100 MGy. Then, the PEEK film substrate was
allowed to stand in a vacuum for 24 hours at 200.degree. C. A
crosslinked film substrate obtained in this manner was insoluble in
concentrated sulfuric acid. On the other hand, an untreated PEEK
film substrate rapidly dissolved in concentrated sulfuric acid. The
crosslinked PEEK film substrate was allowed to stand in a
1,2-dichloroethane solution of 0.2M chlorosulfonic acid for 24
hours at 0.degree. C., and then hydrolyzed by washing with water,
to obtain a crosslinked aromatic polymer electrolyte membrane. The
ion exchange capacity, water uptake, proton conductivity, methanol
permeability, chemical stability, and tensile strength of the
crosslinked aromatic polymer electrolyte membrane obtained in the
present Example are shown in Table 1.
TABLE-US-00001 TABLE 1 Characteristics of the polymer electrolyte
membrane Chemical Degree Ion stability of exchange Water Proton
Methanol (weight Tensile grafting capacity uptake conductivity
permeability remaining strength (%) (mmol/g) (%) (S/cm) (10.sup.-6
cm.sup.2/s) rate) (MPa) Ex. 1 -- 1.5 51 0.092 1.96 93 58 Ex. 2 --
1.1 29 0.051 1.23 96 52 Ex. 3 37 1.89 57 0.19 1.58 94 42 Ex. 4 37
1.19 27 0.058 0.34 100 63 Ex. 5 43 1.23 31 0.066 0.54 99 57 Comp.
Preparation of electrolyte membrane was impossible, because the
film Ex. 1 substrate rapidly dissolved in the sulfonating solution
Comp. 37 1.93 197 0.083 Not 51 Not Ex. 2 measurable measurable
Comp. 43 1.67 216 0.096 Not 67 Not Ex. 3 measurable measurable
Comp. -- 0.91 32 0.063 8.84 100 37 Ex. 4
Example 2
[0081] A crosslinked aromatic polymer electrolyte membrane obtained
by the same procedure as in Example 1 was further heat-treated in a
vacuum for 2 hours at 180.degree. C. This measure resulted in the
reaction of some of the sulfonic acid groups, obtaining a
multiple-crosslinked aromatic electrolyte membrane having a sulfone
group-crosslinked structure. The ion exchange capacity, water
uptake, proton conductivity, methanol permeability, chemical
stability, and tensile strength of the multiple-crosslinked
aromatic polymer electrolyte membrane obtained in the present
Example are shown in Table 1.
Example 3
[0082] A 2 cm.times.3 cm polyether ether ketone (hereinafter
referred to as PEEK) film substrate (thickness 25 .mu.m) was placed
in a separable glass container with a cock, and deaerated therein,
whereafter the interior of the glass container was purged with an
argon gas. In this state, the PEEK film substrate was irradiated
with .gamma.-rays from a .sup.60Co radiation source at a radiation
dose of 30 kGy at room temperature. Then, 20 g of a 1-propanol
solution of 50 wt. % styrene, which had been deaerated by bubbling
an argon gas, was added into the glass container so that the
irradiated PEEK film substrate would be immersed. After purging
with an argon gas, the glass container was hermetically sealed, and
allowed to stand for 24 hours at 80.degree. C. The resulting graft
polymer film substrate was washed with cumene. The degree of
grafting was calculated from the weight of the film substrate after
drying. This graft film substrate was subjected to electron-beam
crosslinking and sulfonation under the same conditions as in
Example 1 to obtain a crosslinked aromatic polymer electrolyte
membrane. The degree of grafting, ion exchange capacity, water
uptake, proton conductivity, methanol permeability, chemical
stability, and tensile strength of the crosslinked aromatic polymer
electrolyte membrane obtained in the present Example are shown in
Table 1.
Example 4
[0083] A crosslinked aromatic polymer electrolyte membrane obtained
by the same procedure as in Example 3 was further heat-treated in a
vacuum for 2 hours at 180.degree. C. This treatment resulted in the
reaction of some of the sulfonic acid groups, obtaining a
multiple-crosslinked aromatic polymer electrolyte membrane having a
sulfone group-crosslinked structure. The degree of grafting, ion
exchange capacity, water uptake, proton conductivity, methanol
permeability, chemical stability, and tensile strength of the
multiple-crosslinked aromatic polymer electrolyte membrane obtained
in the present Example are shown in Table 1.
Example 5
[0084] A 2 cm.times.3 cm polyether imide (hereinafter referred to
as PEI) film substrate (thickness 50 pm) was placed in a separable
glass container with a cock, and deaerated therein, whereafter the
interior of the glass container was purged with an argon gas. In
this state, the PEI film substrate was irradiated with .gamma.-rays
from a .sup.60Co radiation source at a radiation dose of 30 kGy at
room temperature. Then, 20 g of a 1-propanol solution of 50 wt. %
styrene, which had been deaerated by bubbling an argon gas, was
added into the glass container so that the irradiated PEI film
substrate would be immersed. After purging with an argon gas, the
glass container was hermetically sealed, and allowed to stand for
24 hours at 80.degree. C. The resulting graft polymer film
substrate was washed with cumene. The degree of grafting was
calculated from the weight of the film substrate after drying. This
grafted PEI film substrate was fixed to an irradiation stand and,
in this state, irradiated with electron-beams (30 mA, voltage 1 MV)
for 10 minutes at a radiation dose of 20 MGy. Then, the grafted PEI
film substrate was allowed to stand in a 1,2-dichloroethane
solution of 0.2M chlorosulfonic acid for 24 hours at 0.degree. C.,
and then hydrolyzed by washing with water, to obtain a crosslinked
aromatic polymer electrolyte membrane. The resulting crosslinked
aromatic polymer electrolyte membrane was heat-treated in a vacuum
under the same conditions as in Example 4. The degree of grafting,
ion exchange capacity, water uptake, proton conductivity, methanol
permeability, chemical stability, and tensile strength of the
crosslinked aromatic polymer electrolyte membrane obtained in the
present Example are shown in Table 1.
Comparative Example 1
[0085] A 2 cm.times.3 cm PEEK film substrate (25 .mu.m) was treated
under the same sulfonation conditions as in Example 1, without
crosslinking by ionizing radiation. This film substrate completely
dissolved in the reaction solution, failing to provide an aromatic
polymer electrolyte membrane.
Comparative Example 2
[0086] A 2 cm.times.3 cm PEEK film substrate (25 .mu.m) was
subjected to the same method as in Example 3 to introduce styrene
graft chains into it. The graft film substrate was treated under
the same sulfonation conditions as in Example 3, without
crosslinking by ionizing radiation. An aromatic polymer electrolyte
membrane obtained in this manner had low mechanical strength, and
had difficulty in maintaining a membranous shape. The degree of
grafting, ion exchange capacity, water uptake, proton conductivity,
methanol permeability, and chemical stability of the aromatic
polymer electrolyte membrane obtained in the present Comparative
Example are shown in Table 1.
Comparative Example 3
[0087] A 2 cm.times.3 cm PEI film substrate (50 .mu.m) was
subjected to the same method as in Example 5 to introduce styrene
graft chains into it. The graft film substrate was treated under
the same sulfonation conditions as in Example 3, without
crosslinking by ionizing radiation. An aromatic polymer electrolyte
membrane obtained in this manner had low mechanical strength, and
had difficulty in maintaining a membranous shape. The degree of
grafting, ion exchange capacity, water uptake, proton conductivity,
methanol permeability, and chemical stability of the polymer
electrolyte membrane obtained in the present Comparative Example
are shown in Table 1.
Comparative Example 4
[0088] DuPont's Nafion 112, which is a perfluorinated polymer
electrolyte membrane now in widest use for polymer electrolyte fuel
cells, was measured for ion exchange capacity, water uptake, proton
conductivity, methanol permeability, chemical stability, and
tensile strength, under the above-mentioned conditions. These data
are shown in Table 1.
[0089] The results in Table 1 show that the polymer electrolyte
membranes of the Examples are low in water uptake, satisfactory in
proton conductivity, low in methanol permeability, satisfactory in
chemical stability, and high in tensile strength, as compared with
those of the Comparative Examples.
[0090] The crosslinked aromatic polymer electrolyte membrane of the
present invention has both of the characteristics of a crosslinked
polymer and those of an aromatic polymer. Thus, it is an
electrolyte membrane possessing low water uptake, high proton
conductivity, low methanol permeability, high chemical stability,
and excellent mechanical characteristics. In its manufacturing
process, a highly crosslinked structure is imparted beforehand to
the aromatic polymer film substrate, or the monomer-grafted
aromatic polymer film substrate. Thus, the film substrate can be
sulfonated directly in the sulfonating solution. Compared with the
methods of the related art including the complicated waste acid
treating and membrane-forming steps, therefore, the cost of
manufacturing can be markedly reduced. Moreover, the
microphase-separated structure of the polymer electrolyte membrane
can be designed by selecting the film substrate within a wide
range, controlling the degree of sulfonation, or controlling the
degree of grafting. Thus, it can be expected to provide a polymer
electrolyte membrane optimal for a fuel cell for mobile
instruments, a fuel cell for stationary cogeneration systems, or a
fuel cell for automobiles, which utilizes methanol, hydrogen or the
like as a fuel. The economic effect of the polymer electrolyte
membrane is great.
[0091] The invention thus described, it will be obvious that the
same may be varied in many ways. Such variations are not to be
regarded as a departure from the spirit and scope of the invention,
and all such modifications as would be obvious to one skilled in
the art are intended to be included within the scope of the
following claims.
* * * * *