Electrospinning and Post-Spun Chain Conformations of Synthetic, Hydrophobic Poly(α-amino acid)s.

Electrospinning and post-spun conformations of hydrophobic poly(α-amino acid)s are described in this study. The poly(α-amino acid)s, poly(Gly), poly(L-Ala), poly(L-Val), and poly(L-Leu) were synthesized via corresponding N-carboxy-a-amino acid anhydrides. The average molecular weight and degree of polymerization of these polymers were determined by N-terminus labeling using 2,4-dinitrofluorobenzene and by viscometry in the case of poly(Gly). These poly(α-amino acid)s were electrospun from trifluoroacetic acid or trifluoroacetic acid/dichloromethane solutions. The FT-IR spectroscopy and wide-angle X-ray diffraction indicated that the electrospun poly(L-Ala) and poly(L-Leu) fibers predominantly adopts α-helical structure, whereas poly(L-Val) and poly(Gly) fibers exhibited mainly β-strand and random coil structures, respectively

STUDIES ON THE INHIBITIVE EFFECT OF 3-HYDROXYFLAVONE ON THE ACID CORROSION OF MILD STEEL

The corrosion inhibition effect of 3-hydroxyflavone was studied on mild steel in 1 M hydrochloric acid (HCl). The anticorrosive effect was evaluated by weight loss and electrochemical methods which include Tafel polarization and AC impedance studies at 300 K. In weight loss method, the inhibition efficiency increased with increase in inhibitor concentration, and decreased with increase in temperature and immersion time, and acid concentration. The inhibitor showed maximum efficiency of 91% at 4 × 10-4 M concentration in 1 M hydrochloric acid. The Tafel polarization study showed that the inhibitor behaves likely as cathodic type. The corrosion inhibition effect measured by weight loss method and electrochemical studies was in good agreement with each other. The surface analysis was done by using scanning electron microscope (SEM). Several adsorption isotherms are assessed to study the adsorption behavior of the inhibitor on the mild steel surface. The negative value of ΔGads indicates the spontaneous adsorption of the inhibitor on mild steel surface.Adsorption isotherm, corrosion inhibition, electrochemical studies, 3-hydroxyflavone

Electrospinning and Post-Spun Chain Conformations of Synthetic, Hydrophobic Poly(α-amino acid)s

Electrospinning and post-spun conformations of hydrophobic poly(α-amino acid)s are described in this study. The poly(α-amino acid)s, poly(Gly), poly(l-Ala), poly(l-Val), and poly(l-Leu) were synthesized via corresponding N-carboxy-α-amino acid anhydrides. The average molecular weight and degree of polymerization of these polymers were determined by N-terminus labeling using 2,4-dinitrofluorobenzene and by viscometry in the case of poly(Gly). These poly(α-amino acid)s were electrospun from trifluoroacetic acid or trifluoroacetic acid/dichloromethane solutions. The FT-IR spectroscopy and wide-angle X-ray diffraction indicated that the electrospun poly(l-Ala) and poly(l-Leu) fibers predominantly adopts α-helical structure, whereas poly(l-Val) and poly(Gly) fibers exhibited mainly β-strand and random coil structures, respectively

Facile Synthesis of Core/Shell-like NiCo2O4-Decorated MWCNTs and its Excellent Electrocatalytic Activity for Methanol Oxidation

Aulario en la Ciudad Universitaria. Madrid. Convocatoria Abril. Plan 1996. Proyecto fin de carrera. Universidad Politécnica de Madrid. Escuela Técnica Superior de Arquitectur

Ruthenium(II) 9,10-phenanthrenequinone thiosemicarbazone complexes: synthesis, characterization, and catalytic activity towards the reduction as well as condensation of nitriles

<div><p>The ligands 9,10-phenanthrenequinone-N⁴-substituted thiosemicarbazones (HL_1–3) and their ruthenium(II) complexes were synthesized and characterized by elemental and spectroscopic methods. The ligands are tridentate, monobasic chelating ligands with O, N, and S as the donor sites and are in the thiol form in all the complexes. Catalytic studies showed that all the complexes displayed good catalytic activity towards the reduction of nitriles and also the condensation of nitriles with 2-aminoalcohol under solvent-free conditions.</p></div

FT-IR spectroscopy of Ch and DMAB(P)-Ch.

<p>FT-IR spectroscopy of Ch and DMAB(P)-Ch.</p

Effect of Microgravity on Fungistatic Activity of an α-Aminophosphonate Chitosan Derivative against <i>Aspergillus niger</i>

<div><p>Biocontamination within the international space station is ever increasing mainly due to human activity. Control of microorganisms such as fungi and bacteria are important to maintain the well-being of the astronauts during long-term stay in space since the immune functions of astronauts are compromised under microgravity. For the first time control of the growth of an opportunistic pathogen, <i>Aspergillus niger</i>, under microgravity is studied in the presence of α-aminophosphonate chitosan. A low-shear modelled microgravity was used to mimic the conditions similar to space. The results indicated that the α-aminophosphonate chitosan inhibited the fungal growth significantly under microgravity. In addition, the inhibition mechanism of the modified chitosan was studied by UV-Visible spectroscopy and cyclic voltammetry. This work highlighted the role of a bio-based chitosan derivative to act as a disinfectant in space stations to remove fungal contaminants.</p></div

Schematic representation of synthesis of α-aminophosphonate chitosan derivative.

<p>Schematic representation of synthesis of α-aminophosphonate chitosan derivative.</p