New Inhibitor Based on Hydrolyzed Keratin Peptides for Stainless Steel Corrosion in Physiological Serum: An Electrochemical and Thermodynamic Study.

Reducing the impact of some biological fluids on bioimplants involves the control of surface characteristics by modeling the interface architecture and assembling ecofriendly thin films to retard corrosion. Therefore, a mixture of hydrolyzed keratin peptides (HKER) was investigated as a corrosion inhibitor for 304L stainless steel (SS) in physiological serum (PS), using electrochemical measurements associated with optical microscopy and atomic force microscopy (AFM). The tests, performed for various concentrations of the inhibitor at different temperatures, showed that the inhibition efficiency () decreased with a rise in temperature and proportionally increased with the HKER concentration, reaching its maximum level, around 88%, at 25 °C, with a concentration of 40 g L HKER in physiological serum.

Anchoring of Copper(II)-Schiff Base Complex in SBA-15 Matrix as Efficient Oxidation and Biomimetic Catalyst.

A new mononuclear Cu(II) complex [Cu(L)(HO)], where L is the Schiff base 2-[2-(3-bromopropoxy)benzylideneamino] benzoic acid, was synthesized and covalently anchored onto an amino-functionalized SBA-15 mesoporous silica in order to obtain an efficient heterogeneous catalyst. The elemental, structural, textural and morphological characterization confirmed the coordination of the central Cu(II) ion with two ligands and two HO molecules in the synthesized complex and its successful immobilization into the inner pore surface of the NH-functionalized support without the loss of the mesoporous structure. The catalytic activity of the free or immobilized Cu(II) complex was tested in the oxidation of cyclohexene with HO under an air atmosphere and the dismutation reaction of the superoxide radical anions with very good results.

Experimental and Computational Study on Inhibitory Effect and Adsorption Properties of -Acetylcysteine Amino Acid in Acid Environment.

Potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) were applied to study the inhibitory effect of -acetylcysteine (NAC) on corrosion inhibition of carbon steel in hydrochloric acid solution. -acetylcysteine influenced the iron dissolution to a greater extent than the hydrogen evolution reaction acting as a mixed inhibitor, predominantly anodic. The charge transfer resistance (R) gradually increased with the inhibitor concentration.

Cu(II) and Mn(II) Anchored on Functionalized Mesoporous Silica with Schiff Bases: Effects of Supports and Metal-Ligand Interactions on Catalytic Activity.

New series of Cu(II) and Mn(II) complexes with Schiff base ligands derived from 2-furylmethylketone (Met), 2-furaldehyde (Fur), and 2-hydroxyacetopheneone (Hyd) have been synthesized in situ on SBA-15-NH, MCM-48-NH, and MCM-41-NH functionalized supports. The hybrid materials were characterized by X-ray diffraction, nitrogen adsorption-desorption, SEM and TEM microscopy, TG analysis, and AAS, FTIR, EPR, and XPS spectroscopies. Catalytic performances were tested in oxidation with the hydrogen peroxide of cyclohexene and of different aromatic and aliphatic alcohols (benzyl alcohol, 2-methylpropan-1-ol, and 1-buten-3-ol).

Bioactive Co(II), Ni(II), and Cu(II) Complexes Containing a Tridentate Sulfathiazole-Based () Schiff Base.

New Co(II), Ni(II), and Cu(II) complexes were synthesized with the Schiff base ligand obtained by the condensation of sulfathiazole with salicylaldehyde. Their characterization was performed by elemental analysis, molar conductance, spectroscopic techniques (IR, diffuse reflectance and UV-Vis-NIR), magnetic moments, thermal analysis, and calorimetry (thermogravimetry/derivative thermogravimetry/differential scanning calorimetry), while their morphological and crystal systems were explained on the basis of powder X-ray diffraction results. The IR data indicated that the Schiff base ligand is tridentate coordinated to the metallic ion with two N atoms from azomethine group and thiazole ring and one O atom from phenolic group.

Transition Metal(II) Complexes with Cefotaxime-Derived Schiff Base: Synthesis, Characterization, and Antimicrobial Studies.

New [ML2(H2O)2] complexes, where M = Co(II), Ni(II), Cu(II), and Zn(II) while L corresponds to the Schiff base ligand, were synthesized by condensation of cefotaxime with salicylaldehyde in situ in the presence of divalent metal salts in ethanolic medium. The complexes were characterized by elemental analyses, conductance, and magnetic measurements, as well as by IR and UV-Vis spectroscopy. The low values of the molar conductance indicate nonelectrolyte type of complexes.