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[EN] The paper reports the crucial role of the morphology of poly(3,4-ethylenedioxythiophene) (PEDOT) nanostructures on the thermal and dielectric properties of polymer blends prepared thereof. PEDOT nanostructures with two different morphologies (nanoparticles and nanowires) were synthesized. The size for the nanoparticles was in the range 10 40 nm and the diameter of the nanowires was of ca. 200 nm. These nanostructures were blended with an insulating polymer matrix, poly(methyl methacrylate) (PMMA), to evaluate the dielectrical properties of the materials. The results of broadband dielèctric spectroscopy showed a strong correlation between the morphology of the nanostructure and the improvement of the electrical properties of the material.

The aim of the present paper is to explore the potential of radical-mediated dehydrogenation of bile salts (BSs), which is reminiscent of the enzymatic action of hydroxysteroid dehydrogenase enzymes (HSDH). The concept has been demonstrated using triplet carbonyls that can be efficiently generated upon selective UVA-excitation. Hydrogen atom transfer (HAT) from BSs to triplet benzophenone (BP) derivatives gave rise to radicals, ultimately leading to reduction of the BP chromophore with concomitant formation of the oxo-analogs of the corresponding BSs. The direct reactivity of triplet BP with BSs in the initial step was evaluated by determining the kinetic rate constants using laser flash photolysis (LFP). The BP triplet decay was monitored (lambda(max) = 520 nm) upon addition of increasing BS concentrations, and the obtained rate constant values indicated a reactivity of the methine hydrogen atoms in the order of C-3 < C-12 < C-7. The steady-state kinetics of the overall process, monitored through the disappearance of the typical BP absorption band at 260 nm, was much faster under N-2 than under O-2, also supporting the role of the oxygen-quenchable triplet in the dehydrogenation process. Furthermore, irradiation of deaerated aqueous solutions of sodium cholate in the presence of KPMe provided the oxo-analogs, 3[O], 7[O]-CA, 3[O]-CA and 7[O]-CA, arising from the HAT process.

The aim of the present paper is to explore the potential of radical-mediated dehydrogenation of bile salts (BSs), which is reminiscent of the enzymatic action of hydroxysteroid dehydrogenase enzymes (HSDH). The concept has been demonstrated using triplet carbonyls that can be efficiently generated upon selective UVA-excitation. Hydrogen atom transfer (HAT) from BSs to triplet benzophenone (BP) derivatives gave rise to radicals, ultimately leading to reduction of the BP chromophore with concomitant formation of the oxo-analogs of the corresponding BSs. The direct reactivity of triplet BP with BSs in the initial step was evaluated by determining the kinetic rate constants using laser flash photolysis (LFP). The BP triplet decay was monitored (lambda(max) = 520 nm) upon addition of increasing BS concentrations, and the obtained rate constant values indicated a reactivity of the methine hydrogen atoms in the order of C-3 < C-12 < C-7. The steady-state kinetics of the overall process, monitored through the disappearance of the typical BP absorption band at 260 nm, was much faster under N-2 than under O-2, also supporting the role of the oxygen-quenchable triplet in the dehydrogenation process. Furthermore, irradiation of deaerated aqueous solutions of sodium cholate in the presence of KPMe provided the oxo-analogs, 3[O], 7[O]-CA, 3[O]-CA and 7[O]-CA, arising from the HAT process.

[EN] The paper reports the crucial role of the morphology of poly(3,4-ethylenedioxythiophene) (PEDOT) nanostructures on the thermal and dielectric properties of polymer blends prepared thereof. PEDOT nanostructures with two different morphologies (nanoparticles and nanowires) were synthesized. The size for the nanoparticles was in the range 10 40 nm and the diameter of the nanowires was of ca. 200 nm. These nanostructures were blended with an insulating polymer matrix, poly(methyl methacrylate) (PMMA), to evaluate the dielectrical properties of the materials. The results of broadband dielèctric spectroscopy showed a strong correlation between the morphology of the nanostructure and the improvement of the electrical properties of the material.

Single track-etched conical nanopores in polymer foils have attracted considerable attention in recent years due to their potential applications in biosensing, nanofluidics, information processing, and other fields. The performance of a nanopore critically depends on the size and shape of its narrowest, nanometer-sized region. In this paper, we reconstructed the profiles of both doubly-conical and conical pores, using an algorithm based on conductometric measurements performed in the course of etching, coupled with SEM data. We showed that pore constriction deviates from the conical shape, and the deviation depends on the energy loss of the particle that produced the track. Funnel-like profiles of tracks of four ions with different atomic numbers were derived from experimental data. The simulations, using a Poisson–Nernst–Planck model, demonstrated that the ion current rectification properties of the funnel-shaped asymmetrical pores significantly differ from those of conical ones if the tip radius of the pore is smaller than 10 nm. Upon subjecting to further etching, the pores gradually approach the ‘‘ideal’’ conical geometry, and the ion transport properties of these two pore configurations become almost indistinguishable.

Single track-etched conical nanopores in polymer foils have attracted considerable attention in recent years due to their potential applications in biosensing, nanofluidics, information processing, and other fields. The performance of a nanopore critically depends on the size and shape of its narrowest, nanometer-sized region. In this paper, we reconstructed the profiles of both doubly-conical and conical pores, using an algorithm based on conductometric measurements performed in the course of etching, coupled with SEM data. We showed that pore constriction deviates from the conical shape, and the deviation depends on the energy loss of the particle that produced the track. Funnel-like profiles of tracks of four ions with different atomic numbers were derived from experimental data. The simulations, using a Poisson–Nernst–Planck model, demonstrated that the ion current rectification properties of the funnel-shaped asymmetrical pores significantly differ from those of conical ones if the tip radius of the pore is smaller than 10 nm. Upon subjecting to further etching, the pores gradually approach the ‘‘ideal’’ conical geometry, and the ion transport properties of these two pore configurations become almost indistinguishable.

[EN] In this paper we report on the one-pot transformation of glycerol into acrylic acid, catalyzed by W/V mixed oxides, with hexagonal tungsten bronze (HTB) structure. The reaction requires two different catalyst functions, i.e., an acid one, which is given by W oxide, and an oxidizing one, given by the V ions incorporated within the WO3 lattice. W¿O bronze is very active and moderately selective in acrolein formation, but yields only traces of acrylic acid. The incorporation of increasing amounts of V inside the hexagonal tungsten bronze structure, with the development of a monophasic compound, allows the consecutive oxidation of acrolein into acrylic acid. An optimal atomic ratio between W and V equal to V/(W + V) = 0.12¿0.21 made it possible to obtain an acrylic acid yield of 25% (with selectivity to residual acrolein of 11%). However, during reaction under the oxygen-containing feed, the V4+ incorporated into the hexagonal bronze structure underwent a slow oxidation into V5+, which caused a progressive decline of selectivity to acrylic acid and a concomitant increase of COx formation; the hexagonal structure however was stable during lifetime experiments. On the other hand, in the absence of oxygen a very rapid deactivation of the catalyst occurred, with a decrease in selectivity to acrolein and increase in heavy by-products.

[EN] In this paper we report on the one-pot transformation of glycerol into acrylic acid, catalyzed by W/V mixed oxides, with hexagonal tungsten bronze (HTB) structure. The reaction requires two different catalyst functions, i.e., an acid one, which is given by W oxide, and an oxidizing one, given by the V ions incorporated within the WO3 lattice. W¿O bronze is very active and moderately selective in acrolein formation, but yields only traces of acrylic acid. The incorporation of increasing amounts of V inside the hexagonal tungsten bronze structure, with the development of a monophasic compound, allows the consecutive oxidation of acrolein into acrylic acid. An optimal atomic ratio between W and V equal to V/(W + V) = 0.12¿0.21 made it possible to obtain an acrylic acid yield of 25% (with selectivity to residual acrolein of 11%). However, during reaction under the oxygen-containing feed, the V4+ incorporated into the hexagonal bronze structure underwent a slow oxidation into V5+, which caused a progressive decline of selectivity to acrylic acid and a concomitant increase of COx formation; the hexagonal structure however was stable during lifetime experiments. On the other hand, in the absence of oxygen a very rapid deactivation of the catalyst occurred, with a decrease in selectivity to acrolein and increase in heavy by-products.