Evaluation of Some Inorganic Anions and Organic Compounds as Corrosion Inhibitors of Cu-Zn Alloys in H2SO4 and HNO3 Solutions

Evaluation of inorganic and organic compounds as corrosion inhibitors of Cu-Zn alloys in H2 SO4 and HNO3 solutions was studied using potentiodynamic and impedance spectroscopy along with scanning electron microscope (SEM) and energy dispersive X-Ray analyzer (EDX) investigations. The corrosion inhibition of Cu-Zn alloys was investigated in oxy acid solutions using inorganic potassium permanganate and di-hydrogen phosphate, amino acids as environmentally safe materials, commercial cooling water, and green tea extracts. Both potassium permanganate and di-hydrogen phosphate improve the corrosion resistance of Cu-Zn alloys. Phosphate appears more effective as corrosion inhibitor for Cu-Zn alloys than permanganate. The inhibition efficiency (IE%) of the different amino acids such as valine, leucine and lysine was also calculated. The experimental results have shown that amino acid-like lysine can be used as an efficient corrosion inhibitor for the Cu-Zn alloys in oxy acid solutions. This may be due to the presence of two amino groups adsorbed together. For lysine, inhibition efficiency, IE%, of ~87 and ~59 is for H2SO4 and ~96.3 and 54.9 for HNO3 for alloy I and II respectively are observed. Due to the composition of green water have a great effect on the inhibition action on Cu-Zn alloys which reaching 91.8 and 96.5% for Alloy I and 95.4 and 87.1% for Alloy II in 0.5 M H2 SO4 and HNO3 respectively. Although benzotriazole, in cooling water, is an excellent inhibitor suitable for use in a wide variety of environments, it has toxic properties. So, much of the recent researches have focused on formulating new and more environmentally acceptable preservation solutions. The green tea, as plant extract, will be very environmentally friendly. The EDX confirm the formation of a protective layer on the Cu-Zn alloys containing aluminum in Alloy II. This sequence reflects the beneficial effects of Al in Alloy II. The presence of 2.43% Al in Alloy II improves the corrosion resistance due to the formation of thin, transparent, stable and self-healing Al2 O3 layer. This confirmed the results obtained from the potentiodynamic polarization measurements and EIS methods

Enhancement of corrosion protection of AISI 201 austenitic stainless steel in acidic chloride solutions by Ce-doped TiO₂ coating

Abstract Ce-doped TiO₂ coatings were applied by electrodeposition on a low-nickel austenitic stainless steel (AISI 201) bearing 8 wt% Mn to improve the electrochemical properties in acidic chloride solutions. Characterization of the Ce-doped TiO₂ coatings was performed by a scanning electron microscope equipped with energy dispersive X-ray spectroscopy (EDS) to study the tiny features. The corrosion behavior of the bare and coated steel was evaluated in aqueous acidic chloride solutions mixing with different chloride concentrations, 1 mol·L⁻¹ H₂SO₄ with 0–1.5% NaCl. Potentiodynamic polarization tests were conducted to evaluate the corrosion characteristics, corrosion potential Ecorr and corrosion current density icorr. Further study concerning the weight loss (WL) using immersion tests for the long-term was conducted to determine the bare and corresponding coated steel's equivalent corrosion rates. It was found that the electrodeposited Ce-doped TiO₂ coatings with a layer thickness of ~1 μm enhance the corrosion resistance of the coated steel in the acidic chloride solutions compared to its counterpart, the bare steel. The polarization tests showed that the icorr of the Ce-doped TiO₂ coated steel significantly declined to a half value of the bare steel. The Ecorr for all coated specimens shifted to a more positive value when compared with those of the bare steel. The WL measurements displayed that the bare AISI 201 steel experiences intensive corrosion degradation in the presence of a low concentration of chloride ions. However, the Ce-doped TiO₂ coatings significantly resist the aggressive chloride ions and consequently increase the corrosion resistance of the steel

Anticancer Activities of Newly Synthesized Chiral Macrocyclic Heptapeptide Candidates

As important cancer therapeutic agents, macrocyclic peptides have recently drawn great attention, mainly because they are synthetically accessible and have lower toxicity towards normal cells. In the present work, we synthesized newly macrocyclic pyridoheptapeptide derivatives. The synthesized derivatives were characterized using standard chemical and spectroscopic analytical techniques, and their anticancer activities against human breast and hepatocellular cancer cells were investigated. Results showed that compounds 1a and 1b were the most effective against hepatocellular (HepG2) and breast (MCF-7) cancer cell lines, respectively

Design, Synthesis and Docking Studies of Novel Macrocyclic Pentapeptides as Anticancer Multi-Targeted Kinase Inhibitors

A series of macrocyclic pyrido-pentapeptide candidates 2–6 were synthesized by using N,N-bis-[1-carboxy-2-(benzyl)]-2,6-(diaminocarbonyl)pyridine 1a,b as starting material. Structures of the newly synthesized compounds were established by IR, 1H and 13C-NMR, and MS spectral data and elemental analysis. The in-vitro cytotoxicity activity was investigated for all compounds against MCF-7 and HepG-2 cell lines and the majority of the compounds showed potent anticancer activity against the tested cell lines in comparison with the reference drugs. Out of the macrocyclic pyrido-pentapeptide based compounds, 5c showed encouraging inhibitory activity on MCF-7 and HepG-2 cell lines with IC50 values 9.41 ± 1.25 and 7.53 ± 1.33 μM, respectively. Interestingly, 5c also demonstrated multitarget profile and excellent inhibitory activity towards VEGFR-2, CDK-2 and PDGFRβ kinases. Furthermore, molecular modeling studies of the compound 5c revealed its possible binding modes into the active sites of those kinases