Proton-Conducting Polymeric Membranes Based on 1,2,4-Triazole

In this review, a comparative analysis of the literature and our own results obtained in the study of the physicochemical, dielectric, and proton-conducting properties of composite polymer materials based on 1H-1,2,4-triazole has been carried out. It has been established that 1H-1,2,4-triazole and homopolymers and copolymers of 1-vinyl-1,2,4-triazole are promising for the development of proton-conducting fuel cell membranes. They significantly improve the basic characteristics of electrolyte membranes, increase their film-forming ability, increase thermal stability up to 300–330 °C, increase the electrochemical stability region up to 3–4 V, promote high mechanical strength and morphological stability of membranes, and provide high ionic conductivity (up to 10−3–10−1 S/cm) under anhydrous conditions at temperatures above 100 °C. There is also an improvement in the solubility and a decrease in the glass transition temperature of polymers based on 1-vinyl-1,2,4-triazole, which facilitates the processing and formation of membrane films. The results obtained demonstrate the uniqueness of 1H-1,2,4-triazole and (co)polymers based on 1-vinyl-1,2,4-triazole and the promise of their use for the creation of heat-resistant plastic and electrochemically stable, mechanically strong proton-conducting membranes with high ionic conductivity under anhydrous conditions and at high temperatures

Proton-Conducting Polymeric Membranes Based on 1,2,4-Triazole

In this review, a comparative analysis of the literature and our own results obtained in the study of the physicochemical, dielectric, and proton-conducting properties of composite polymer materials based on 1H-1,2,4-triazole has been carried out. It has been established that 1H-1,2,4-triazole and homopolymers and copolymers of 1-vinyl-1,2,4-triazole are promising for the development of proton-conducting fuel cell membranes. They significantly improve the basic characteristics of electrolyte membranes, increase their film-forming ability, increase thermal stability up to 300–330 °C, increase the electrochemical stability region up to 3–4 V, promote high mechanical strength and morphological stability of membranes, and provide high ionic conductivity (up to 10−3–10−1 S/cm) under anhydrous conditions at temperatures above 100 °C. There is also an improvement in the solubility and a decrease in the glass transition temperature of polymers based on 1-vinyl-1,2,4-triazole, which facilitates the processing and formation of membrane films. The results obtained demonstrate the uniqueness of 1H-1,2,4-triazole and (co)polymers based on 1-vinyl-1,2,4-triazole and the promise of their use for the creation of heat-resistant plastic and electrochemically stable, mechanically strong proton-conducting membranes with high ionic conductivity under anhydrous conditions and at high temperatures

Mechanochemical Synthesis and DC Electrical Conductivity of PANI-Based MWCNT Containing Nanocomposites with Te⁰ and Bi₂Te₃ Thermoelectric Nanophase

Nowadays, the search for the coupled polymer nanocomposite thermoelectrics that exhibit a high value of thermoelectric figure of merit (ZT) and similar behaviour of physical properties for the use as legs of thermoelectric cells is a current challenge. The direct current (DC) conductivity is one of the three important components of thermoelectric figure of merit. The aim of this study was to obtain PANI-based nanothermoelectrics with Te0 and Bi2Te3 nanoparticles and MWCNT by mechanochemical methodology and to investigate the dependency of their DC electrical conductivity on temperature in the 298–353 K range using the Arrhenius and Mott’s variable range hopping (VRH) models. Inorganic Te0 and Bi2Te3 nanoparticles were pre-synthesized by the available and environmentally friendly method using a commercial tellurium powder. The samples obtained were characterized by X-ray diffractometry (XRD), IR and UV-Vis spectroscopy. The XRD study of ES-PANI/Te0 (4.4 wt% Te0) and ES-PANI/Bi2Te3 (2.9 wt% Bi2Te3) nanocomposites found that the nanoparticle average size was 32 nm and 17 nm, respectively. The DC conductivity study of the samples with different nanophase content (2.1, 4.4, 10.2 wt% Te0, 1.5, 2.9, 7.3 wt% Bi2Te3, 1.5 wt% MWCNT) by the two points measurement method reveals the following: (a) the presence of inorganic nanophase reduces the conductivity compared to the matrix, (b) the addition of MWCNT in ES-PANI increases its electrical conductivity, (c) the conductivity of ES-PANI/Te0 as well as ES-PANI/Bi2Te3 nanocomposite rises with the increasing inorganic nanophase content, (d) the observed increase in the electrical conductivity of MWCNT-based nanocomposites with increasing inorganic nanophase content is interrupted by a characteristic area of decrease in its value at average values of inorganic nanoparticles content (at Te0 content of 4.4 wt%, at Bi2Te3 content of 2.9 wt%), (e) a similar DC conductivity behaviour in ES-PANI/Te0—ES-PANI/Bi2Te3 and ES-PANI/Te0-MWCNT—ES-PANI/Bi2Te3-MWCNT nanocomposite pairs is observed

One-Pot Preparation of Metal–Polymer Nanocomposites in Irradiated Aqueous Solutions of 1-Vinyl-1,2,4-triazole and Silver Ions

Metal–polymer nanocomposite polyvinyltriazole–silver nanoparticles were obtained using one-pot synthesis in irradiated aqueous solutions of 1-vinyl-1,2,4-triazole (VT) and silver ions. Gel permeation chromatography data show that upon radiation initiation, the molecular weight of poly(1-vinyl-1,2,4-triazole) increases with increasing monomer concentration. To study the kinetics of polymerization and the features of the radiation–chemical formation of nanoparticles, UV-Vis spectroscopy was used. TEM images show a relatively small average size of the forming nanoparticles (2–3 nm) and a narrow size distribution, which shows the effective stabilization of nanoparticles by triazole substituents at a molar ratio of VT and silver ions of 25/1. The addition of ethyl alcohol was used to increase the efficiency of synthesis and suppress the crosslinking of macromolecules in solution. The results of the work show that aqueous–alcoholic solutions of 1 wt.% VT can be used to obtain soluble nanocomposite materials. 10 wt.% monomer solutions have prospects for use in the preparation of polymer gels filled with nanoparticles

Synthesis and Characterization of Silver-Containing Nanocomposites Based on 1-Vinyl-1,2,4-triazole and Acrylonitrile Copolymer

Insoluble silver-containing nanocomposites based on 1-vinyl-1,2,4-triazole and acrylonitrile copolymer was synthesized and characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, atomic absorption, X-ray diffraction, and thermogravimetric data analysis. The silver content of the nanocomposites varied from 8.0 to 23.5% (the silver content depends on the ratio of the copolymer-silver salt). Synthesis of silver nanocomposites was carried out by thermal treatment of a polymer complex of copolymer-silver salt without the use of an additional reducing agent. X-ray diffraction was used to control the formation of silver nanoparticles at different temperatures (210°С, 220°С, and 250°С). Synthesis of nanocomposites shows a developed porous structure with a channel diameter in most cases of 1-4 microns. The EPR monitoring of the nanoparticle germination and growth reveals that the generation of the nanocomposites proceeds via a stage of complex formation between the polymeric matrix and silver ions. The synthesized nanocomposites possess paramagnetic properties and show a narrow EPR symmetric signal with the concentration of unpaired electrons of 1020 spin/g, a g-factor 2.0050, and signal width 5-6 Gs. Thermal stability of silver-containing nanocomposites is up to 270-320°C

Evaluation of the Safety and Toxicity of the Original Copper Nanocomposite Based on Poly-N-vinylimidazole

A new original copper nanocomposite based on poly-N-vinylimidazole was synthesized and characterized by a complex of modern physicochemical and biological methods. The low cytotoxicity of the copper nanocomposite in relation to the cultured hepatocyte cells was found. The possibility to involve the copper from the nanocomposite in the functioning of the copper-dependent enzyme systems was evaluated during the incubation of the hepatocyte culture with this nanocomposite introduced to the nutrient medium. The synthesized new water-soluble copper-containing nanocomposite is promising for biotechnological and biomedical research as a new non-toxic hydrophilic preparation that is allowed to regulate the work of key enzymes involved in energy metabolism and antioxidant protection as well as potentially serving as an additional source of copper

Composite Hydrogels Based on Bacterial Cellulose and Poly-1-vinyl-1,2,4-triazole/Phosphoric Acid: Supramolecular Structure as Studied by Small Angle Scattering

New composite hydrogels (CH) based on bacterial cellulose (BC) and poly-1-vinyl-1,2,4-triazole (PVT) doped with orthophosphoric acid (oPA), presenting interpenetrating polymeric networks (IPN), have been synthesized. The mesoscopic study of the supramolecular structure (SMS) of both native cellulose, produced by the strain Komagataeibacter rhaeticus, and the CH based on BC and containing PVT/oPA complex were carried out in a wide range of momentum transfer using ultra- and classical small-angle neutron scattering techniques. The two SMS hierarchical levels were revealed from 1.6 nm to 2.5 μm for the objects under investigation. In addition, it was shown that the native BC had a correlation peak on the small-angle scattering curves at 0.00124 Å−1, with the correlation length ξ being equal to ca. 510 nm. This motive was also retained in the IPN. The data obtained allowed the estimation of the fractal dimensions and ranges of self-similarity and gave new information about the BC mesostructure and its CH. Furthermore, we revealed them to be in coincidence with Brown’s BC model, which was earlier supported by Fink’s results