Insights into the use of two novel supramolecular compounds as corrosion inhibitors for stainless steel in a chloride environment: experimental as well as theoretical investigation.

Novel supramolecular (SCPs) compounds such as: {[Ni (EIN)4(NCS)2]}, SCP1 and {[Co (EIN)4 (NCS)2]}, SCP2 have been studied using weight loss (WL) and electrochemical tests on the corrosion performance of stainless steel 304 (SS304) in 1.0 M hydrochloric acid (HCl) solution. The experimental results revealed that inhibition efficacy (η%) rises with increasing concentrations of SCPs and reached 92.3% and 89.6% at 16 × 10-6 M, 25 °C, from the WL method for SCP1 and SCP2, respectively. However, by raising the temperature, η% was reduced. Polarization measurements (PDP) showed that the SCPs molecules represent a mixed-type. The SCPs were adsorbed on a SS304 surface physically, and the Langmuir adsorption isotherm was found to govern the adsorption process. The determination of thermodynamic parameters was carried out at various temperatures. Quantum chemical calculations were calculated to prove the adsorption process of SCP components, using the molecular dynamics (MD) simulations and electron density map. The inhibition performance of SCPs for SS304 dissolution in an acidic medium was proved to be excellent through FT-IR and AFM analysis. The results obtained from all measurements exhibit a high level of agreement with each other.

Nano-metal-organic frameworks as corrosion inhibitors for strengthening anti-corrosion behavior of carbon steel in a sulfuric acid environment: from synthesis to applications.

In order to demonstrate the effect of Nano-metal organic frameworks, [Cu2(CN)4(Ph3Sn) (Pyz2-caH)2] (NMOF1) and [∞3[Cu(CN)2(Me3Sn)(Pyz)]] (NMOF2) as corrosion inhibitors for C-steel in 0.5 M sulfuric acid solutions, the following methods were utilized: mass reduction (MR), potentiodynamic polarization (PDP), and AC electrochemical impedance (EIS). The results of the experiments showed that by increasing the dose of these compounds, the inhibition efficacy (η%) of C-steel corrosion increased and reached 74.4-90% for NMOF2 and NMOF1 at a dose of 25 × 10-6 M, respectively. On the other hand, the η% decreased as the temperature range rose. Parameters for activation and adsorption were determined and discussed. Both NMOF2 and NMOF1 were physically adsorbed on the surface of C-steel and conformed to the Langmuir adsorption isotherm model. The PDP studies revealed that these compounds functioned as mixed type inhibitors, i.e. affecting both metal dissolution and hydrogen evolution reactions. Attenuated Total Reflection Infra-Red (ATR-IR) analysis was carried out to determine the morphology of the inhibited C-steel surface. There is good agreement between the findings of EIS, PDP and MR.

The organotin coordination polymer [(n-Bu3Sn)4Fe(CN)6H2O] as effective catalyst towards the oxidative degradation of methylene blue.

The structure of the supramolecular coordination polymer SCP 1; [(n-Bu3Sn)4Fe(CN)6H2O] consists of octahedral [Fe(CN)6](4-) building blocks which are connected by the TBPY-5 configured n-Bu3Sn(CN..)2 fragments creating 3D-network structure. Fenton and photo-Fenton oxidative discoloration of Methylene Blue (MB) has been investigated by hydrogen peroxide catalyzed with the SCP 1. The reaction exhibited pseudo first-order kinetics with respect to each of MB and H2O2. The irradiation of the reaction with UV-light enhanced the rate of MB mineralization, Kobs=0.76 h(-1). Mineralization of MB was investigated by FT-IR spectra. Disodium salt of terephthalic acid photoluminescence probing technology was carried out to identify the reactive oxygen species. The different parameters that affect MB degradation rate were evaluated. Moreover, the efficiency of recycled the SCP 1 and the mechanism of degradation of MB dye were investigated.