Yu. A. Volkova

Synthesis and molecular-mass characteristics of some cardo poly(benzimidazoles)

The GPC procedure for analyzing molecular mass characteristics of cardo poly(benzimidazoles) has been developed. In most cases, the reaction between 4,4′-oxydibenzene-1,2-diamine and 4,4′-(3-oxo-1,3-dihydroisobenzofuran-1,1-diyl)dibenzoic acid in Eaton’s reagent is accompanied by formation of a microgel. Depending on the synthesis conditions (temperature, duration of heating, and content of phosphorus pentoxide in the reaction mixture), polymers with both unimodal and bimodal molecular mass distributions can be prepared. Formation of the microgel fraction is observed for many representatives of poly(benzimidazoles) of various chemical structures. Based on the experimental evidence, the most probable pathway is suggested for the branching side reaction of poly(benzimidazoles) during their synthesis in Eaton’s reagent.

Design of electrodes based on a carbon nanofiber nonwoven material for the membrane electrode assembly of a polybenzimidazole-membrane fuel cell

23 The creation of electrodes for hydrogen–air fuel cells with a polymer electrolyte membrane is a com plex challenge, both fundamental, and scientific and technical. Increase in the fuel cell efficiency directly depends on the quality of the electrodes. Whereas the heart of such a fuel cell is usually believed to be a pro ton conducting membrane, the drive of the fuel cell should be considered to be carbon gas diffusion elec trodes (GDEs) containing nanosized platinum parti cles as an electrocatalyst. Approaches to designing GDEs are quite versatile, but generally reduce to the application of a catalytic ink (aqueous dispersions of perfluoropolymers and electrocatalysts (Pt/C)) to a carbon paper or tissue with a perfluorinated hydro phobic microporous layer [1, 2].

Chemical modification of cardo poly(benzimidazole) using “click” reaction for membranes of high-temperature hydrogen fuel cells

Phosphonethylated poly(benzimidazole)s (PEP BIs) were obtained for the first time in the Nesmey anov Institute of Organoelement Compounds, Rus sian Academy of Sciences, by the polymer analogous reaction of high molecular weight PBI–O–PT poly mer [3] via the reaction with O,O diethyl vinylphos phonate [4] (Scheme 1) and successfully studied in the construction of the membrane electrode block (MEB) of the hydrogen HTFC.

Synthesis and studies of polybenzimidazoles for high-temperature fuel cells

A number of polybenzimidazoles (PBIs) were synthesized and tested in real fuel cells. The possibility of introducing phosphoric groups in PBIs was studied. The phosphorylated and fluorine-containing PBIs obtained by click reactions were investigated.

Electrospun nanofiber pyropolymer electrodes for fuel cells on polybenzimidazole membranes

After the deposition of Pt on their surface, the carbon nanofiber materials synthesized by sequential oxidation and pyrolysis of electrospun nanofiber mats based on polyacrylonitrile are used as the gas-diffusion electrodes for high-temperature hydrogen–air fuel cells on a polybenzimidazole (PBI) proton-conducting membranes. In contrast to the traditional methods of electrode preparation in which the catalyst (Pt) nanoparticles are localized on the surface of carbon black which is applied as “ink” on the conducting support (carbon paper or tissue), in this study the Pt nanoparticles are being deposited and developed on the surface carbon nanofibers to form a combined gas-diffusion material. In the tests, the resulting electrodes demonstrate good efficiency within hydrogen-air fuel cells on the PBI membrane.

Molecular Mass Characteristics and Solution Behavior of Some Cardo Polybenzimidazoles

The behavior of dilute solutions of cardo polybenzimidazoles based on 3,3′4,4′-tetraaminodiphenyl ether; 3,3′,4,4′-tetraaminodiphenyl sulfone; and 4,4′-diphenylphthalidedicarboxylic acid in solvents of various natures has been studied by the methods of dynamic light scattering, sedimentation, and viscometry. All of the polymers have been found to contain a microgel fraction. For each fraction, the diffusion coefficient and the particle size are determined. The experimental characteristics of macromolecules correspond to the conformational rigidity calculated by a computer simulation procedure.

Development of methanol–air fuel cells with membrane materials based on new sulfonated polyheteroarylenes

New proton-conducting membranes were synthesized from sulfonated polynaphthoyleneimide (SPNI) and polytriazole (SPTA), which are of interest for use in portable methanol fuel cells. The membrane electrode assembly (MEA) based on SPNI and SPTA showed power and voltage-current characteristics comparable to those of MEA based on Nafion®-117. The direct and reverse polarization curves coincided almost completely in shape, indicating that the obtained characteristics are stable. At a voltage of 0.3 V and a temperature of 40°С, the current density and power density reached 68 mA cm–2 and 20.5 mW cm–2, respectively.

Study of ionic conductivity of polytriazole and polynaphthalenediimide ion-exchange membranes

Transport properties of the new polytriazole and polynaphthalenediimide membrane materials have been observed. According to impedance data, the sulfonated polynaphthalenediimide membrane obtained in dimethylsulfoxide demonstrates the maximum value of ionic conductivity. Modification of a membrane material with silica leads to transport properties improvement.

Synthesis of condensed pregnano[17,16-d]triazolines under high pressure

Condensed pregnano[17,16-d]triazolines were produced in 1,3-dipolar cycloaddition of 16-dehydropregnenolone acetate with organic azides at 10 kbar. The structure of the synthesized compounds was determined by using two-dimensional NMR spectroscopy (1H—1H COSY, NOESY, HSQC, and HMBC).

Ionic Conductivity of Ceria-Doped Ion Exchange Membranes on the Basis of Sulfonated Polynaphthaleneimide

Hybrid membrane materials on the basis of sulfonated polynaphthaleneimide doped with ceria have been synthesized, and their ionic conductivity has been investigated. The conditions for membrane synthesis with different dopant contents have been determined. Ceria doping leads to a decrease in the ionexchange capacity of membranes and an increase in their ion conductivity upon contact with water. After 7% ceria doping, the ionic conductivity of the initial membrane (1.9 × 10−2 Ω−1 cm−1) increases up to 3.0 × 10−2 Ω−1 cm−1.