Carboxylated perfluorinated ionomer membranes

Structure of Sulfonated and Carboxylated Perfluorinated Ionomer Membranes... 

SouKe Hashimoto, T. et al., Structure of sulfonated and carboxylated perfluorinated ionomer membranes, in Peifluorinated Ionomer Membranes, American Chemical Society, Vol. 180, 1982, pp. 217-248. 

Table II. Properties of Carboxylic-Acid Form of Perfluorinated Ionomer Membranes as a Function of Equivalent Weight.

I, 1980, 76, 2558-2574 L.Y. Levy, A. Jenard and H.D. Hurwitz, Hydration and ion-exchange process in carboxylic membranes. Part 1. Infrared spectroscopic investigation of the acid membranes, J. Chem. Soc. Trans. 1, 1982, 78, 29-36 M. Falk, Infrared spectra of perfluorosulfonated polymer and water in perfluorosulfonate polymer, Perfluorinated Ionomer Membranes, ed. A. Eisenberg, H.L. Yeager, ACS Symposium Series, American Chemical Society, Washington DC, 1982, p. 139 C. Heitner-Wirguin and D. Hall, An infrared study of an anion exchange membrane,... 

Hensley, J. E. and Way, J. D. 2007. Synthesis and characterization of perfluorinated carboxylate/sulfonate ionomer membranes for separation and solid electrolyte applications. Chemistry of Materials 19 ... 

A good measure of past and continuing interest in ionomer membranes issued from the development of perfluorinated ionomers, the first-announced being Nafion(44). These materials are characterized by remarkable chemical resistance, thermal stability and mechanical strength, and they have a very strong acid strength, even in the carboxylic acid form. The functionalities that have been considered include carboxylate, sulfonate, and sulfonamide, the latter resulting from the reactions of amines with the sulfonyl fluoride precursor. 

Since the conductivity of electrolytes and the cross section and thickness of the membrane are known, a can be determined from the voltage drops across the three pairs of probe electrodes 1-2, 3-4 and 5-6. The sodium current efficiency (CE) can also be determined by titrating the amount of caustic soda generated over a given period of time. The confinement chambers around the working electrodes are used to eliminate free bubbles near the membrane. Our normalized transport data for sulfonate, carboxylate and sulfonamide ionomers are plotted In Figure 5 the universal percolative nature of perfluorinated ionomers can be clearly eeij. The prefactor sulfonate ionomers. The exponent t is 1.5 0.1 in reasonable agreement with theory and the thresholds are between 8 to 10 vol. %, which are consistent with the bimodal distribution in cluster size postulated by the cluster-network model (5.18). This theory has also been applied recently to delineate sodium selectivity of perfluorinated ionomers (20). 

These performance goals have now largely been attained by continued improvements through several generations of materials. Currently, commercial perfluorinated ionomer materials for this application consist of membranes with carboxylate or mixed carboxylate-sulfonate functionality the latter membranes often have layered structures with the carboxylate layer exposed to the caustic catholyte solution. Fabric reinforcement is used in some instances to improve strength. 

Perfluorinated ionomers such as Nafion are of significant commercial importance as cation exchange membranes in brine electrolysis cells ( 1). Outstanding chemical and thermal stability make this class of polymers uniquely suited for use in such harsh oxidizing environments. The Nafion polymer consists of a perfluorinated backbone and perfluoroalkylether sidechains which are terminated with sulfonic acid and/or carboxylic acid functionality. 

The perfluorinated, carboxylated and sulfonated ionomer membranes form the ionic clusters of a few nm in size, as in the case of the hydrocarbon-based ionomers such as polyethylene,polystyrene and polybutadiene(9). The ionic clusters strongly affect physical properties of the membranes, e.g., the swelling behavior of the membranes (amount of water uptaken by the membranes, W and... 

In perfluorinated ionomers, a PTFE-based polymeric backbone offers chemical stability from the radical species or acid-base, which causes hydrolytic degradation of the polymer chain. Ionic conductivity is provided by pendant acidic moiety in carboxylate or sulfonate form. There are some reports on perfluorinated carboxylic acid (PFCA) materials, most of which are derived from Nafion [26-29]. However, PFCA is not suitable for fuel cell application due to its low proton conductivity. Perfluorosulfonic acid (PFSA) is the most favored choice among not only perfluorinated membranes but all other ionomers in fuel cell applications. Sulfonic acid form of Nafion is a representative PFSA and thus has been intensively studied since 1960s. Reported chemical structure of Nafion membrane is given in Fig. 13.8. 

Ionomers are used to prepare membranes for a variety of applications including dialysis, reverse osmosis, and in electrolytic cells for the chlor-alkali industry. This latter application needs materials that show good chemical resistance and ionomers based on perfluorinated backbones with minor amounts of sulfonic or carboxylic acids are ideal. They also show good ion-exchange properties. 

Ion clusters are commonly observed in the ionized forms of the perfluorinated membranes. The size of the clusters appears to be larger for sulfonate than for carboxylate membranes." " The size increases in the order Na, and Cs" and decreases with increasing number of functional groups per chain and with increasing temperature.As in the case of ethylene ionomers, the perfluorinated carboxylic acid membranes do not form ion clusters, at least in the dry state." The electrostatic interaction may be too weak to form ionic clusters. These observations are expected according to the Eisenberg theory (see Section II.2). 

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