Corrosion Activity of Carbon Steel B450C and Low Chromium Ferritic Stainless Steel 430 in Chloride-Containing Cement Extract Solution

The carbon steel B450C and low chromium SS 430 ferritic samples were exposed for 30 days to chloride-containing (5 g L−1 NaCL) cement extract solution. The initial pH ≈ 13.88 decreased to pH ≈ 9.6, associated mainly with the consumption of OH− ions and the formation of γ-FeOOH, α-FeOOH, Fe3O4 and Cr(OH)3, as suggested by XRD and XPS analysis, in the presence of CaCO3 and NaCl crystals. The deep corrosion damages on B450C were observed around particles of Cu and S as local cathodes, while the first pitting events on the SS 430 surface appeared after 30 days of exposure. The change in the activity of each type of steel was provided by the potentiodynamic polarization curves (PDP). Two equivalent electrical circuits (EC) were proposed for quantitative analysis of EIS (Nyquist and Bode diagrams). The calculated polarization resistance (Rp), as an indicator of the stability of passive films, indicated that SS 430 presented relatively constant values, being two-three orders of magnitude higher than those of the carbon steel B450C. The calculated thickness (d) of the SS 430 passive layers was ≈0.5 nm and, in contrast, that of the B450C passive layers tends to disappear after 30 days.

Electrocatalysts Based on Novel Carbon Forms for the Oxidation of Sulphite

Described herewith is an electrochemical method to decontaminate sulphur compounds. Studies were carried out of sulphites (SO32−) oxidation on a range of anode catalysts. The electrocatalysts were characterized by scanning electron microscopy, XRD, XPS and BET. Polarization curves were recorded of electrodes incorporating lyophilized higher fullerenes and manganese oxides. The experiments showed that lyophilized higher fullerenes and C60/C70 fullerene catalysts in conjunction with manganese oxides electrochemically convert sulphites (SO32−) to sulphates (SO42−). The oxidation products do not poison the electrodes. The XPS analysis shows that the catalysts incorporating DWCNTs, MWCNTs and higher fullerenes have a higher concentration of sp3C carbon bonding leading to higher catalytic activity. It is ascertained that higher fullerenes play a major role in the synthesis of more effective catalysts. The electrodes built by incorporating lyophilized catalysts containing higher fullerenes and manganese oxides are shown as most promising in the effective electrochemical decontamination of industrial and natural wastewaters.

Mussel-inspired Coating of α-AlH3: A Compact Structure with Highly Enhanced Stability

we present a novel surfacing coating to resolve the stability of α-AlH3. Inspired by the strong chemical adhesion of mussels, the polymerization of dopamine was first introduced to coat α-AlH3 through a simple situ polymerization. The α-AlH3 was used as a substrate. In-depth characterizations confirmed compact formation with PDA on α-AlH3 surface. The coated α-AlH3 sample was characterized by XRD XPS and SEM . The results show that a strong PDA film is formed on the surface of α-AlH3, the PDA@α-AlH3 retained primary morphology. The crystal form of α-AlH3 does not change after coated by PDA. The results of XPS analysis show that N1s appears on the material after coated by PDA, indicating that polydopamine is formed on the surface of α-AlH3. The moisture absorption tests show that the moisture absorption rate of α-AlH3 is greatly reduced after being coated with PDA. The excellent intact ability of PDA prevent α-AlH3 reacting with watered in the air. The thermal stability of α-AlH3 before and after coating was analyzed by DSC. This work demonstrates the successful applications of dopamine chemistry to α-AlH3, thereby providing a potential method for the metastable materials.

Plasma Co-Polymerization of HMDSO and Limonene with an Atmospheric Pressure Plasma Jet

Plasma co-polymers (co-p) were deposited with an atmospheric pressure plasma jet (APPJ) using a precursor mixture containing hexamethyldisiloxane (HMDSO) and limonene. A coating with fragments from both precursors and with siloxane, carbonyl and nitrogen functional groups was deposited. The flow rate of limonene was found to be an important parameter for plasma co-polymerization to tune the formation and structure of the functional groups. The FTIR and XPS analysis indicates that with increasing flow rate of limonene a higher proportion of carbon is bound to silicon. This is related to a stronger incorporation of fragments from limonene into the siloxane network and a weaker fragmentation of HMDSO. The formation mechanism of the nitroxide and carboxyl groups can be mainly differentiated into in-plasma and post-plasma reactions, respectively.

Effect of (NH4)2ZrF6, Voltage and Treating Time on Corrosion Resistance of Micro-Arc Oxidation Coatings Applied on ZK61M Magnesium Alloys

The effects of (NH4)2ZrF6 concentration, voltage and treating time on the corrosion resistance of ZK61M magnesium alloy micro-arc oxidation coatings were studied by orthogonal experiments. The SEM result shows that the surface roughness and porosity of MAO coatings increased with (NH4)2ZrF6 concentration, voltage and treating time as a whole, except the porosity decreased with treating time. EDS, XRD and XPS analysis show that (NH4)2ZrF6 was successfully incorporated into coatings by reactive incorporation, coatings are dominantly composed of ZrO2, MgO, MgF2 and amorphous phase Mg phosphate. Potentiodynamic polarization was used to evaluate the corrosion property of coatings. When the concentration of (NH4)2ZrF6 is 6 g/L, the voltage is 450 V, and the treating time is 15 min, the coating exhibits the best corrosion resistance which corrosion current density is four magnitudes lower than substrate attributed to the incorporation of ZrO2 and the deposition of MgF2 in the micropores.

Synthesis of Fe:Ag nanocomposites and their anti-bacterial activities

The present study reports the synthesis of Fe:Ag composite nanoparticles by green approach, utilizing Urtica dioica leaves extract, as reducing and capping agent for the metal sources. Formation of composite phases found to depend on the salt sources, which provides different ion species in the reaction mixture. The formation of crystalline nanoparticles having cubic structure was confirmed by XRD analysis. Ag rich crystalline nanoparticles were found to disperse in the oxidized Fe matrix by high resolution transmission microscopic studies. XPS analysis revealed the presence of Fe of in 0, +2, and +3 valance states and Ag in Ag+1 and Ag° states. The synthesized nanoparticles were found to show notable antibacterial activity against the gram negative pathogen E. Coli and gram positive pathogen S. aureus.

UV/Ozone Treatment and Open-Air Copper Plasmonics

Thin copper films with thickness ∼28 nm deposited on SiO2 substrate with the vacuum electron beam evaporation method and treated by UV-ozone are studied. It was found that a UV-ozone treatment of the copper film causes rapid formation of the thin ∼3-4 nm oxide film. XPS analysis showed that CuO oxide predominates in this film. The formed oxide film effectively protects the copper against the following oxidation. The presented method of UV-ozone treatment is a simpler and cheaper approach compared to many other ways to form protective coatings of copper to preserve its functional properties. This method can be useful in nanoelectronic, nanooptical, and biosensors applications.

Flexible Diodes/Transistors Based on Tunable p-n-Type Semiconductivity in Graphene/Mn-Co-Ni-O Nanocomposites

We report a novel Mn-Co-Ni-O (MCN) nanocomposite in which the p-type semiconductivity of Mn-Co-Ni-O can be manipulated by addition of graphene. With an increase of graphene content, the semiconductivity of the nanocomposite can be tuned from p-type through electrically neutral to n-type. The very low effective mass of electrons in graphene facilitates electron tunneling into the MCN, neutralizing holes in the MCN nanoparticles. XPS analysis shows that the multivalent manganese ions in the MCN nanoparticles are chemically reduced by the graphene electrons to lower-valent states. Unlike traditional semiconductor devices, electrons are excited from the filled graphite band into the empty band at the Dirac points from where they move freely in the graphene and tunnel into the MCN. The new composite film demonstrates inherent flexibility, high mobility, short carrier lifetime, and high carrier concentration. This work is useful not only in manufacturing flexible transistors, FETs, and thermosensitive and thermoelectric devices with unique properties but also in providing a new method for future development of 2D-based semiconductors.