Patent Application
20100044616
The field to which the disclosure generally relates includes polymer electrolyte and fuel cells.
Polymer electrolytes play an important part in electrochemical devices such as batteries and fuel cells. To achieve optimal performance, the polymer electrolyte must maintain a high ionic conductivity and mechanical stability at both high and low relative humidity. The polymer electrolyte also needs to have excellent chemical stability for long product life and mechanical robustness. Fluorinated copolymers have been explored as electrolytes for fuel cells. Due to their inherent chain configuration, however, low equivalent weight fluorinated copolymers typically suffer from water swelling at high humidity and excess membrane shrinkage at low humidity. A low equivalent weight fluorinated random copolymer membrane lacks the mechanical robustness to withstand the rigors of hydration and dehydration within an operating fuel cell. Thus, there is a need for an improved polymer electrolyte that maintains robust mechanical properties and high ionic conductivity at wide range of humidity conditions.
Accordingly, an improved polymer electrolyte molecular architecture and a process of synthesizing such a polymer electrolyte are desired.
The present invention solves one or more problems of the prior art by providing in at least one embodiment a polymer blend including a first polymer that includes a non-ionic polymer segment and a second polymer having the following chemical moiety:
Advantageously, the polymer blends provide improved fuel cell performance at lower cost, reduced water volume swells in boiling water, improved elasticity, mechanical properties and durability, and reduced reactant gas cross-over. In addition, the blends allow thin membranes to be cast with improved ease of handling. Moreover, the need for ePTFE support structures is eliminated. Finally, the blends of the present embodiment cast from dimethylacetamide allow membrane formation without an annealing step at 140° C. as required for membranes cast from aqueous alcohol.
Other exemplary embodiments of the invention will become apparent from the detailed description provided hereinafter. It should be understood that the detailed description and specific examples, while disclosing exemplary embodiments of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.
Exemplary embodiments of the present invention will become more fully understood from the detailed description and the accompanying drawings, wherein:
Reference will now be made in detail to presently preferred compositions, embodiments and methods of the present invention, which constitute the best modes of practicing the invention presently known to the inventors. The Figures are not necessarily to scale. However, it is to be understood that the disclosed embodiments are merely exemplary of the invention that may be embodied in various and alternative forms. Therefore, specific details disclosed herein are not to be interpreted as limiting, but merely as a representative basis for any aspect of the invention and/or as a representative basis for teaching one skilled in the art to variously employ the present invention.
Except in the examples, or where otherwise expressly indicated, all numerical quantities in this description indicating amounts of material or conditions of reaction and/or use are to be understood as modified by the word “about” in describing the broadest scope of the invention. Practice within the numerical limits stated is generally preferred. Also, unless expressly stated to the contrary: percent, “parts of,” and ratio values are by weight; the term “polymer” includes “oligomer,” “copolymer,” “terpolymer,” and the like; the description of a group or class of materials as suitable or preferred for a given purpose in connection with the invention implies that mixtures of any two or more of the members of the group or class are equally suitable or preferred; description of constituents in chemical terms refers to the constituents at the time of addition to any combination specified in the description, and does not necessarily preclude chemical interactions among the constituents of a mixture once mixed; the first definition of an acronym or other abbreviation applies to all subsequent uses herein of the same abbreviation and applies mutatis mutandis to normal grammatical variations of the initially defined abbreviation; and, unless expressly stated to the contrary, measurement of a property is determined by the same technique as previously or later referenced for the same property.
It is also to be understood that this invention is not limited to the specific embodiments and methods described below, as specific components and/or conditions may, of course, vary. Furthermore, the terminology used herein is used only for the purpose of describing particular embodiments of the present invention and is not intended to be limiting in any way.
It must also be noted that, as used in the specification and the appended claims, the singular form “a,” “an,” and “the” comprise plural referents unless the context clearly indicates otherwise. For example, reference to a component in the singular is intended to comprise a plurality of components.
Throughout this application, where publications are referenced, the disclosures of these publications in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains.
With reference to
In an embodiment of the present invention, a polymer blend includes a first polymer having a non-ionic polymer segment and second polymer having the following chemical moiety:
In a variation, the first polymer is a non-ionic polymer.
In a variation of an exemplary embodiment, the polymer blend further includes a non-ionic polymer such as a fluoroelastomer. The fluoroelastomer may be any elastomeric material comprising fluorine atoms. The fluoro-elastomer may comprise a fluoropolymer having a glass transition temperature below about 25° C. or preferably, below 0° C. The fluoro-elastomer may exhibit an elongation at break in a tensile mode of at least 50% or preferably at least 100% at room temperature. The fluoro-elastomer is generally hydrophobic and substantially free of ionic groups. The fluoro-elastomer polymer chain may have favorable interaction with the hydrophobic domain of the second polymer described above. Such favorable interaction may facilitate formation of a stable, uniform and intimate blend of the two materials. The fluoro-elastomer may be prepared by polymerizing at least one fluoro-monomer such as vinylidene fluoride, tetrafluoroethylene, hexafluoropropylene, vinylfluoride, chlorotrifluoroethylene, perfluoromethylvinyl ether, and trifluoroethylene. The fluoro-elastomer may also be prepared by copolymerizing at least one fluoro-monomer and at least one non-fluoro-monomer such as ethylene, propylene, methyl methacrylate, ethyl acrylate, styrene, vinylchloride and the like. The fluoro-elastomer may be prepared by free radical polymerization or anionic polymerization in bulk, emulsion, suspension and solution. Examples of fluoro-elastomers include poly(tetrafluoroethlyene-co-ethylene), poly(vinylidene fluoride-co-hexafluoropropylene), poly(tetrafluoroethylene-co-propylene), terpolymer of vinylidene fluoride, hexafluoropropylene and tetrafluoroethylene, and terpolymer of ethylene, tetrafluoroethylene and perfluoromethylvinylether. Some of the fluoro-elastomers are commercially available from Arkema under trade name Kynar Flex and Solvay Solexis under the trade name Technoflon®, from 3M under the trade name Dyneon®, and from DuPont under the trade name Viton®. For example, Kynar Flex 2751 is a copolymer of vinylidene fluoride and hexafluoropropylene with a melting temperature between about 130° C. and 140° C. The glass transition temperature of Kynar Flex 2751 is about −40 to −44° C. The fluoro-elastomer may further comprise a curing agent to allow crosslinking reaction after blended with the second polymer.
In another exemplary embodiment, the second polymer is a perfluorosulfonic acid polymer (PFSA). In a refinement, the second polymer is a copolymer containing repeating units based on tetrafluoroethylene and repeating units represented by (CF2—CF)—(OCF2CFX)m—Op—(CF2)n—SO3H, where X represents a fluorine atom or a trifluoromethyl group, m represents an integer from 0 to 3, n represents an integer from 1 to 12 and p represents an integer of 0 or 1. Specifically, the first example would be represented by m=1, X═CF3, p=1, n=2; the second example would be represented by m=0, p=1, n=2 and the third example would be represented by m=0, p=1, n=4.
In a further refinement, the second polymer is selected from the group consisting:
where o, p, n, are integers such that there are less than 15 o segments for each p segment.
In another refinement, the second polymer includes at least one of the following polymer segments:
In one refinement, the first polymer is present in an amount from about 1 to about 80 weight percent of the total weight of the polymer blend. In another refinement, the first polymer is present in an amount from about 5 to about 50 weight percent of the total weight of the polymer blend. In another refinement, the first polymer is present in an amount from about 10 to about 30 weight percent of the total weight of the polymer blend. In another refinement, the second polymer is present in an amount from about 20 to about 99 weight percent of the total weight of the polymer blend. In still another refinement, the second polymer is present in an amount from about 50 to about 95 weight percent of the total weight of the polymer blend. In still another refinement, the second polymer is present in an amount from about 30 to about 90 weight percent of the total weight of the polymer blend.
The following examples illustrate the various embodiments of the present invention. Those skilled in the art will recognize many variations that are within the spirit of the present invention and scope of the claims.
Blends of PFSA polymers with polyvinylidene fluoride (PVDF2, Kynar) are solution coated from N,N-dimethylacetamide (DMAc) to form polyelectrolyte membranes at temperatures of between 80° C. and about 95° C. As set forth in
The above description of embodiments of the invention is merely exemplary in nature and, thus, variations thereof are not to be regarded as a departure from the spirit and scope of the invention.
