Sargassum muticum extract based on alginate biopolymer as a new efficient biological corrosion inhibitor for carbon steel in hydrochloric acid pickling environment: Gravimetric, electrochemical and surface studies.

The inhibition effect of the invasive brown seaweed Sargassum muticum extract (ESM), harvested from the Atlantic coast of Morocco, against the corrosion of carbon steel (CS) in 1 M HCl medium was studied for the first time using gravimetric, electrochemical and surface techniques. The methanolic crude extract of Sargassum muticum (ESM) is rich in alginate biopolymer. The evaluation corrosion tests showed that this algal extract acts as a good mixed corrosion inhibitor for CS substrate in 1 M HCl since inhibition efficiency of 97% was reached with 1 g/L of ESM at 303 K. AC impedance findings showed that the seaweed extract adding in the corrosive electrolyte increases the polarization resistance and conversely decreases the charge capacitance at the interface. Adsorption of ESM on the substrate surface followed the Langmuir adsorption isotherm. X-ray photoelectron spectroscopy analyses (XPS) demonstrated that the corrosion inhibition mechanism of CS substrate in 1 M HCl environment by the investigated algal extract is typical of the chemisorption process and the protective barrier is mainly formed by the adsorbed biological macromolecules.

Surface characterization and properties of ordered arrays of CeO2 nanoparticles embedded in thin layers of SiO2.

We demonstrated the surface composite character down to the nanometer scale of SiO(2)-CeO(2) composite high surface area materials, prepared using 5 nm colloidal CeO(2) nanoparticle building blocks. These materials are made of a homogeneous distribution of CeO(2) nanoparticles in thin layers of SiO(2), arranged in a hexagonal symmetry as shown by small-angle X-ray scattering and transmission electron microscopy. Since the preparation route of these composite materials was selected in order to produce SiO(2) wall thickness in the range of the CeO(2) nanoparticle diameter, these materials display surface nanorugosity as shown by inverse chromatography. Accessibility through the porous volume to the functional CeO(2) nanoparticle surfaces was evidenced through an organic acid chemisorption technique allowing quantitative determination of CeO(2) surface ratio. This surface composite nanostructure down to the nanometer scale does not affect the fundamental properties of the functional CeO(2) nanodomains, such as their oxygen storage capacity, but modifies the acid-base properties of the CeO(2) surface nanodomains as evidenced by Fourier transform IR technique. These arrays of accessible CeO(2) nanoparticles displaying high surface area and high thermal stability, along with the possibility of tuning their acid base properties, will exhibit potentialities for catalysis, sensors, etc.

Infrared spectroscopic study on the surface properties of gamma-gallium oxide as compared to those of gamma-alumina.

By hydrolysis of an ethanolic gallium nitrate solution, gamma-Ga2O3 was prepared as a single-phase polymorph having a specific surface area of 160 m2 g(-1). Surface acidity and basicity of this material was studied by IR spectroscopy, using pyridine, 2,6-dimethylpyridine, acetonitrile, and carbon dioxide as spectroscopic probe molecules. For comparison, a gamma-Al2O3 sample having a surface area of 290 m2 g(-1) was also studied. On partially hydroxylated gamma-Ga2O3, the main O-H stretching bands were found at 3693 (sharp) and at 3660-3630 cm(-1) (broad), and the material proved (by adsorbed dimethylpyridine) to have a weak Brønsted acidity. Surface Lewis acidity of gamma-Ga2O3 was revealed (mainly) by adsorbed pyridine, which gave the characteristic IR absorption bands of Lewis-type adducts at 1612, 1579, 1488, and 1449 cm(-1) (values noted under an equilibrium pressure of 1 Torr at room temperature); the corresponding Lewis acid centers (coordinatively unsaturated Ga3+ ions) were found to be weaker, although more abundant, than those present on the surface of gamma-Al2O3 (unsaturated Al3+ ions). Another significant difference between gamma-Ga2O3 and gamma-Al2O3 is the smaller thermal stability of pyridine and 2,6-dimethylpyridine Lewis adducts formed on the gallium oxide. The surface basicity of gamma-Ga2O3 was studied by using carbon dioxide and deuterated acetonitrile as IR probe molecules. Adsorbed CO2 gave carbonate and hydrogen-carbonate surface species similar to those formed by gamma-Al2O3. Adsorbed acetonitrile gave rise to acetamide species, which revealed the basic character of surface O2- ions. These acetamide species were found to be more abundant on gamma-Ga2O3 than on gamma-Al2O3.