In the context of attempts to improve the protection of the environment, a novel process where the carbon dioxide reacts rapidly with almost 100 % conversion under mild conditions, is proposed. The chemisorptive process takes place in a slurry bubble column which operates with countercurrent flow, utilizing special solutions of primary long chain amines in a nonaqueous media. The product obtained is insoluble and separated by filtration. Because of its molecular structure, this product possesses tenside properties and can be used as an industrial additive. Typically the liquid phase consists of a mixture of hexadecylamine (C 16 H 33 NH 2 ) or dodecylamine (C 12 H 25 NH 2 ) in various concentrations with methanol or other alcohols as the solvent. Numerous parameters have been studied including different column heights, gas inlet compositions, gas flow rates and solvent type. Efficiencies of up to 99 % are achievable for CO 2 absorption with methanol as the solvent. The second solvent examined, isopropanol, shows lower CO 2 conversion rates. This can be attributed to its physical properties, mainly higher viscosity and hence, smaller mass transfer coefficient. In order to simulate real gas conditions, the influence of other sour gases, e.g., SO 2 was also investigated experimentally. Because of coabsorption of the two gases, the CO 2 efficiency was lower in this instance. In both solvents, the absorption efficiency with respect to SO 2 is more than 99 % due to its high solubility and reactivity. A complex mathematical model has been developed and applied to describe the mass and enthalpy transport in the reactive bubble column.
A paper by Mi et al. [1] suggested that certain nano-sized hematite (α-Fe 2 O 3 ) particles had diamagnetic properties at room temperature. Since diamagnetic behavior is not a property normally attributed to hematite particles (hematite is generally regarded as a canted antiferromagnetic material at room temperature) we decided to test the validity of the suggestions in [1] by performing magnetic susceptibility and magnetic hysteresis measurements on a series of hematite nanoparticles with average sizes of 8 nm, 30 nm and 40 nm in diameter. We initially considered two possible explanations for the apparent diamagnetic behavior of the nanoparticles in [1]: either 1) the hematite nanoparticles themselves exhibited this unusual diamagnetic behavior, or 2) the diamagnetic response was simply the signal created by a diamagnetic dispersant that was overriding a weak positive magnetic susceptibility signal of the hematite nanoparticles. Our experiments strongly suggested the latter explanation that the apparent "diamagnetic" behavior seen in [1] was caused by a diamagnetic dispersant dominating the magnetic properties of the dispersed hematite nanoparticles.
An attempt was made to obtain boron-containing MAX-phase by the process of self-propagating high-temperature synthesis (SHS) of Ti3AlC2, replacing some carbon atoms by boron atoms. This was conducted by burning powder mixtures (charges) of the composition 3Ti+2Al+2((1-x)C+xB), where x is the fraction of boron atoms (0.10, 0.15, 0.25, 0.50, 0.75, 0.90), replacing the carbon atoms. X-ray diffraction analysis of the products of combustion have shown that the replacement of carbon with boron to half of the content of carbon atoms in the charge (x=0.10-0.50), does not change the phase composition of the products, including Ti3AlC2 and TiC, but leads to a shift of the peaks of these phases in the diffraction pattern in the direction of smaller angles. When replacing more than half of the carbon atoms with the boron (x=0.75 and 0.90), the peaks of titanium carbide and MAX-phase are not observed, and the XRD peaks appear of the titanium borides TiB and TiB2, and intermetallic compound Al3Ti. Photomicrographs obtained with an electron microscope show that the SHS products synthesized from the charge with replacing up to half of the carbon atoms with the boron represent plates with a thickness of about 1 μm typical for MAX-phases, but rounded particles of borides and intermetallic compound of titanium appear at a higher boron content. Based on these results, it is concluded that replacement of a part (up to 50%) of the carbon atoms with boron atoms in the SHS charge 3Ti+2Al+2C leads to the synthesis of boron-containing MAX-phase based on the crystal lattice of Ti3AlC2.
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