Search

The electrochemical synthesis of α ${\alpha }$ ‐amino acids at room temperature and pressure is a sustainable alternative to conventional methods like microbial fermentation and Strecker synthesis. A custom‐built zero‐gap flow electrolyzer was used to study the electrosynthesis of alanine via the electrocatalytic reductive amination (ERA) of the corresponding biomass‐derivable α ${\alpha }$ ‐keto acid precursor – pyruvic acid (PA), and hydroxylamine (NH2OH) at very low pH. Non‐toxic, abundant, and easy to prepare TiO2/Ti electrocatalysts were utilized as the cathode. Three TiO2/Ti felt electrodes with different oxide thicknesses were prepared and their characterization results were correlated with their respective electrochemical performance in terms of Faradaic efficiency η ${\eta }$ , and partial current density j‾ ${\left|\overline{j}\right|}$. Cyclic voltammetry indicated a different electrocatalytic reduction process on hydrothermally treated electrodes, compared to thermally oxidized ones. Hydrothermally treated electrodes were also found to have the thickest porous anatase layer and achieved 50–75 % alanine conversion efficiencies. Optimization showed that the cell potential, reactant flow rate and the PA: NH2OH ratio were crucial parameters in determining the conversion efficiency. η ${\eta }$ and j‾ ${\left|\overline{j}\right|}$ were found to significantly decrease when an excess of is used and, an optimal alanine η ${\eta }$ of 75 % was achieved at 2.0 V applied cell potential and 10 mL/h reactant flow rate. [ABSTRACT FROM AUTHOR]

Chitosan microbeads with C-doped TiO2, N-doped TiO2 and C,N-codoped TiO2 were prepared to obtain photocatalysts with higher photocatalytic efficiency, active under visible light and easy to removed from aqueous medium. TiO2 powders were synthesized by the sol–gel method and modified using glucose and ammonium nitrate as source of C and N, respectively. Scanning electron microscope (SEM), X-ray diffraction (XRD), DRUV–Vis spectra and Raman techniques, were used to characterize the modified TiO2 powders. The structural and physicochemical properties of the microbeads were analyzed by nitrogen physisorption, functional groups were identified by Fourier transform Infrared (FT-IR) spectroscopy and microbeads were observed by optical microscopy. The microbeads photocatalytic efficiency under visible light was evaluated monitoring the E. coli growth-inhibition, determined by colony count analysis (CFU—colony forming units). Results showed effectiveness in all tested composites to inhibit E. coli growth in 24 h under visible light. Furthermore chitosan microbeads with C,N-codoped TiO2 showed the best performance in the degradation test being the most effective composite to achieving 99.99% of E. coli growth inhibition in less than 4 h. [ABSTRACT FROM AUTHOR]

The electrochemical synthesis of α ${\alpha }$ -amino acids at room temperature and pressure is a sustainable alternative to conventional methods like microbial fermentation and Strecker synthesis. A custom-built zero-gap flow electrolyzer was used to study the electrosynthesis of alanine via the electrocatalytic reductive amination (ERA) of the corresponding biomass-derivable α ${\alpha }$ -keto acid precursor - pyruvic acid (PA), and hydroxylamine (NH 2 OH) at very low pH. Non-toxic, abundant, and easy to prepare TiO 2 /Ti electrocatalysts were utilized as the cathode. Three TiO 2 /Ti felt electrodes with different oxide thicknesses were prepared and their characterization results were correlated with their respective electrochemical performance in terms of Faradaic efficiency η ${\eta }$ , and partial current density j ‾ ${\left|\overline{j}\right|}$ . Cyclic voltammetry indicated a different electrocatalytic reduction process on hydrothermally treated electrodes, compared to thermally oxidized ones. Hydrothermally treated electrodes were also found to have the thickest porous anatase layer and achieved 50-75 % alanine conversion efficiencies. Optimization showed that the cell potential, reactant flow rate and the PA: NH 2 OH ratio were crucial parameters in determining the conversion efficiency. η ${\eta }$ and j ‾ ${\left|\overline{j}\right|}$ were found to significantly decrease when an excess of is used and, an optimal alanine η ${\eta }$ of 75 % was achieved at 2.0 V applied cell potential and 10 mL/h reactant flow rate., (© 2024 The Authors. ChemPlusChem published by Wiley-VCH GmbH.)