Corrosion inhibition of mild steel in 1 M HCl using water soluble chitosan derivative of vanillin.

The water-soluble chitosan derivative (WSCD) was made by mixing chitosan with sodium hydroxide, treating the mixture with chloroacetic acid, and then forming a Schiff base with vanillin in an acidic medium. In this study, we examined the corrosion-inhibiting ability of a WSCD on mild steel surfaces in acidic environments. Weight loss, EIS, PDP, LPS, and OCP measurements were used to study the corrosion resistance on mild steel surfaces in 1 M HCl solutions with known concentrations of WSCD. The results show that WSCD functions effectively as a mixed-type anodic and cathodic inhibitor, providing 87 % corrosion inhibition efficiency at 75 ppm. Using SEM to investigate the morphology of corroded mild steel with and without varying amounts of WSCD, impedance measurements show the development of a thin film of inhibitor on the metal surface, the extent of which increases as the inhibitor concentration rises. The WSCD molecule first adsorbs on mild steel and follows Langmuir adsorption isotherm. It is found that the (∆Gads0)adsorption's free energy is -17.473 kJ/mol. The contact angle measurements confirm that the hydrophobicity of the metal surface has increased as a result of the inhibitor's thin film development.

On the coordination chemistry of a bacterial siderophore cepabactin from a theoretical perspective.

Iron is one of the essential metals required by almost all living organisms. However, nature has certain constraints in distributing this element among tissues. Since polymeric oxide-bridged Fe (III) is the prominent source of Fe (III) ions, the insolubility of Fe (III) ions in aqueous systems reduces the direct uptake by cells. Secondly, the free-Fe entities which generate .OH radicals pave the way to the destruction of the cells. Hence, a protective coordination environment via sophisticated chemical systems is required for the acquisition of Fe, its successive transport, storage, and effective utilization in various tissues. Siderophores are polydentate ligands used by bacterial cells for Fe acquisition, with a relatively high affinity for Fe (III) ions. Secreted from the bacterial cells into the external aqueous medium, they sequester Fe to give a soluble complex which re-enters the organism at a specific receptor. Once it gets inside the cell, the Fe is released from the complex and utilized for essential biochemical reactions. The medicinal applications of these natural ligands, developing progressively in various research groups, necessitate the theoretical aspects of their coordination chemistry. This research paper deals with the coordination chemistry of one of the siderophores, cepabactin (Cep). The chemical computations confirm that the FeIII(Cep)3 complex is octahedral and high spin. The oxygen atoms of Cep, which are hard and negatively charged, thus act as electron donors in the FeIII(Cep)3 complex formation. This in turn makes the siderophores relatively less attractive towards Fe (II) ions.

Theoretical studies on the coordination chemistry of phytosiderophores with special reference to Fe-nicotianamine complexes in graminaceous plants.

Nicotianamine (NA) is one of the metal-chelating molecules found in higher plants in abundance. Synthesized by the enzyme nicotianamine synthase, NA has a major role in the transport of iron in plant tissues. This research paper deals with the coordination chemistry of the possible complexes of NA, [FeII (NA)]-, and [FeIII (NA)] in detail, from a theoretical standpoint. The chemical computations on the [FeII (NA)]- and [FeIII (NA)] complexes show that NA can bind with both Fe (+ 2) and Fe (+ 3) ions. The calculations confirm that the [FeIII (NA)] is thermodynamically more stable in comparison with [FeII (NA)]-, while [FeII (NA)]- is kinetically more stable than [FeIII (NA)]. Under the physiological conditions prevailing in plant tissues, [FeIII (NA)] can undergo reduction, but the auto-oxidation of [FeII (NA)]- to [FeIII (NA)] is prevented. In summary, NA can translocate Fe ions within plant tissues, wherever required, both as Fe (+ 2) and Fe (+ 3) complexes.

Corrosion inhibition of mild steel using poly (2-ethyl -2-oxazoline) in 0.1M HCl solution.

Effective inhibition of metallic corrosion to prevent its consequent loss is one of the serious apprehensions for industries in the modern world. This paper analyses the application of poly(2-ethyl-2-oxazoline) (PEOX) as an effective inhibitor of corrosion, when it is made to be in contact with the surfaces of mild steel (MS). The sustainability of MS against corrosion in 0.1 M Hydrochloric acid solution in the presence of known concentration of PEOX is assessed by potentiodynamic polarization (PDP) measurements, linear polarization studies (LPR), and electrochemical impedance spectroscopy (EIS). It was observed that PEOX behaves as better inhibitor for mild steel corrosion in 0.1 M HCl solution and it show enhanced inhibition efficiency (IE%) 79% at a concentration of 50 ppm. The polarization experiments indicated that addition of PEOX in concentrations varies from 25 ppm to 50 ppm induces a decrease of both cathodic and anodic currents densities. Also, the micrographs recorded by the Scanning Electron Microscopy confirm that molecules of PEOX act as corrosion inhibitors for the surfaces of MS in 0.1 M HCl. The stability of the MS surface in a corrosion-prone environment is traced by measuring the contact angles of water droplets placed on the MS surface, to quantify the extent of deterioration, if any, due to corrosion. The results presented here show that the compound PEOX performs as a mixed-type inhibitor against corrosion at the MS surface in acidic medium. Theoretical studies based on the electronic structure of PEOX in aqueous medium also support its performance as a successful corrosion-inhibitor.

Supercycled SW(f)-TPPM sequence for heteronuclear dipolar decoupling in solid-state nuclear magnetic resonance.

The performance of a supercycled SW(f)-TPPM sequence for heteronuclear dipolar decoupling in solid-state NMR is analyzed here. The decoupling performance of this sequence with respect to experimental parameters, such as, the phase angle, proton offset and MAS frequency is studied. A comparison is made with two other commonly used decoupling schemes in solid-state NMR namely, SPINAL-64 and SW(f)-TPPM, on a sample of U-¹³C-labeled tyrosine. Our results show that supercycled SW(f)-TPPM performs better than the former sequences. Also, numerical spin dynamics studies are presented which support the experimentally observed efficiency in the decoupling.

Heteronuclear dipolar decoupling in liquid-crystal NMR using supercycled SW(f)-TPPM sequences.

Heteronuclear dipolar decoupling is an essential requirement for extracting structural information from the (13)C NMR spectra of liquid crystals. Efficient schemes for heteronuclear dipolar decoupling in such systems are formulated here by supercycling SW(f)-TPPM, a sequence introduced recently for this purpose in rotating solids. These sequences are compared with two other commonly used decoupling schemes in liquid-crystal NMR, SPINAL-64 and SW(f)-TPPM, by analyzing the intensities of various resonances in the proton decoupled (13)C spectrum of the liquid-crystal 4-n-pentyl-4'-cyanobiphenyl (5CB). The effectiveness of the decoupling programs with respect to experimental parameters such as RF field strength, decoupler offset frequency and phase angle is also presented.