Effects of metal support interaction on dry reforming of methane over Ni/Ce-Al2O3 catalysts

Dry (CO₂) reforming of methane is conducted over two newly synthesized Ni20/Ce-γAl₂O₃ and Ni20/Ce-meso-Al₂O₃ catalysts. The x-ray diffraction (XRD) patterns indicated that Ni20/Ce-meso-Al₂O₃ exhibits a better dispersion of nickel, while Ni20/Ce-γAl₂O₃ has larger amounts of nickel crystallites. The temperature programmed desorption (TPD) kinetics analysis indicated that Ni20/Ce-meso-Al₂O₃ had a lesser metal-support interaction than the Ni20/Ce-γAl₂O₃. The thermal gravimetric analysis (TGA) indicated that the incorporation of ceria into the Al₂O₃ matrix helps to stabilize Ni20/Ce-meso-Al₂O₃ during dry reforming of methane. The temperature programmed reduction (TPR) indicated that the synthesized catalysts were sufficiently reducible below 750 °C. A fixed bed reactor evaluation (at 750 °C) showed that both catalysts can facilitate methane reforming to syngas with minimal coking throughout the 30 hours time-on-stream (TOS). However, Ni20/Ce-meso-Al₂O₃ is more promising in terms of prolonged stability for dry reforming applications. Moreover, the syngas yield for Ni20/Ce-γAl₂O₃ is close to equilibrium prediction during the first 1 hour of reaction time.     

Hierarchical polymer nanocomposite coating material for 316L SS implants: Surface and electrochemical aspects of PPy/f-CNTs coatings

Biocompatible nanocomposite coatings can be synthesized to offer improved surface properties for biomaterials and biomedical implants. Nanocomposite coatings containing polypyrrole (PPy) matrix reinforced with functionalized multi-wall carbon nanotubes (f-CNTs) were deposited on 316L SS substrates using electrochemical route. FT-IR, XRD, SEM, and TEM were employed to characterize the nanocomposite microstructure. High resolution imaging showed relatively uniform dispersion of the CNTs in the nanocomposite with a typical tubular structure. Micro-indentation tests revealed improvement in the hardness of the PPy/CNTs coatings. Measurement of the contact angle indicated enhanced surface wettability of the nanocomposite coatings. The corrosion behavior of 316L SS samples coated with PPy/CNTs was studied in SBF medium. The corrosion potential and the breakdown potential of coated 316L SS substrates shifted to more noble values as compared to uncoated 316L SS samples. The results suggest that incorporating CNTs as reinforcements in PPy coatings can provide enhanced properties in terms of surface hardness, biocompatibility, and corrosion resistance.     

Surface Characterization of Mild Steel During Atmospheric Corrosion After Being Treated by Sodium Dihydrogen Orthophosphate

Protection of Metals and Physical Chemistry of Surfaces - The objective of this study was to characterize the surfaces of the steel products produced locally during their exposure to the industrial...     

Synthesis of Hard Materials by Field Activation: The Synthesis of Solid Solutions and Composites in the TiB2–WB2–CrB2 System

The synthesis of solid solutions of (Ti,W,Cr)B₂ from elemental reactants using the field-activated, pressure-assisted synthesis method and employing the SPS apparatus was investigated. The nature of the products depended on temperature; they were nearly pure solid solutions at 1900°C with minor amounts of β-WB. The product density and microhardness depended on the temperature of synthesis for the same value of applied pressure (64 MPa). Samples with the highest density (94%) corresponded to a hardness of 22.7 GPa. When annealed at 1500°C, the solid solutions decomposed, precipitating a (W,Ti,Cr)B₂ phase in a spinodal form. In addition, β-WB precipitates in the form of thin (0.4–5.3 nm) layers were observed. They existed in a 60°/120° orientation to the (Ti,W,Cr)B₂ matrix, in agreement with previous observations. Highly faceted, small (nanosized) pores associated with the β-WB precipitates were also observed.     

Effect of Product Conductivity on Field-Activated Combustion Synthesis

Experimental and modeling results on the field-activated combustion synthesis (FACS) of Nb₅Si₃ are reported. In the absence of an electric field and without reactant preheating, Nb₅Si₃ cannot be prepared by self-propagating high-temperature synthesis (SHS). Under the influence of a field a self-sustaining combustion wave is established whose rate of propagation decreases with traveled distance. For relatively low field values, the wave propagation mode changes from a continuous (smooth) to a spin mode. The product of synthesis depends on the mode of propagation. Synthesis during continuous wave propagation results in the formation of Nb₅Si₃, primarily in the α-modification. In contrast, when the wave propagates in a spin mode, the product is NbSi₂ with unreacted niobium. The present observations demonstrate a case where the field effect is not localized, as was the case in previous studies. The difference in behavior is attributed to differences in the electrical conductivities of the product phases.     

Inhibition of lipid peroxidation in UVA‐treated skin fibroblasts by luteolin and its glucosides

Ultraviolet A (UVA) radiation causes oxidative damage to human skin cells. This damage may be reduced or prevented using plant compounds as photoprotectants. To investigate the relationship between chemical structure and UVA‐protective activity, three structurally related flavonoids, namely luteolin, luteolin‐7‐O‐glucoside (both present in artichoke) and luteolin‐4'‐O‐glucoside (present in wild carrot), were studied. Human skin fibroblasts exposed to UVA (250 and 500 kJ/m²) were treated with each flavonoid (30 µM) for 18 h prior to irradiation. The extent of lipid peroxidation in the cellular extracts was assessed as lipid peroxides and malondialdehyde (MDA). Luteolin and luteolin‐7‐O‐glucoside both prevented a significant increase in lipid peroxides at 250 kJ/m², but at 500 kJ/m² their effectiveness was clearly attenuated. Contrastingly, luteolin‐4'‐O‐glucoside was pro‐oxidant at both radiation doses. Measurements of MDA levels highlighted that luteolin was clearly more effective than the two glucosides at both 250 and 500 kJ/m². Overall, these results show clear differences between the three flavonoids and suggest that the B ring 3',4'‐dihydroxy group, lacking in luteolin‐4'‐O‐glucoside, may be particularly important. Flavonoid: transition metal ion chelation studies confirmed the influence of the 3',4'‐dihydroxy group, which is also relevant to the quenching of singlet oxygen. These features as well as the greater lipophilic nature of luteolin together explain the superior activity of this flavonoid which may be potentially useful as a supplement in photoprotective skin preparations.     

Heat of combustion of tantalum-tungsten oxide thermite composites

The heat of combustion of two distinctly synthesized stoichiometric tantalum-tungsten oxide energetic composites was investigated by bomb calorimetry. One composite was synthesized using a sol-gel (SG) derived method in which micrometric-scale tantalum is immobilized in a tungsten oxide three-dimensional nanostructured network structure. The second energetic composite was made from the mixing of micrometric-scale tantalum and commercially available (CA) nanometric tungsten oxide powders. The energetic composites were consolidated using the spark plasma sintering (SPS) technique under a 300 MPa pressure and at temperatures of 25, 400, and 500 °C. For samples consolidated at 25 °C, the density of the CA composite is 61.65 ± 1.07% in comparison to 56.41 ± 1.19% for the SG derived composite. In contrast, the resulting densities of the SG composite are higher than the CA composite for samples consolidated at 400 and 500 °C. The theoretical maximum density for the SG composite consolidated to 400 and 500 °C are 81.30 ± 0.58% and 84.42 ± 0.62%, respectively. The theoretical maximum density of the CA composite consolidated to 400 and 500 °C are 74.54 ± 0.80% and 77.90 ± 0.79%, respectively. X-ray diffraction analyses showed an increase of pre-reaction of the constituents with an increase in the consolidation temperature. The increase in pre-reaction results in lower stored energy content for samples consolidated to 400 and 500 °C in comparison to samples consolidated at 25 °C.     

Performance characteristics of Mo–Ni/Al2O3 catalysts in LPG oxidative steam reforming for hydrogen production

A 1:1 propane–butane mixture was used to study the effect of promoting 15 wt.% Ni/Al₂O₃ (15Ni) catalyst with small amounts of Mo (0.05, 0.1, 0.3, and 0.5 wt.%) for H₂ production during LPG oxidative steam reforming. Stability tests at 450 °C showed that lower Mo loadings (0.1 and 0.05 wt.%) had higher conversions and H₂ production rates than the non-promoted catalyst and a stable performance for the whole 18-h test period. TPO results showed that slightly more Ni sites were available for whisker formation over the Mo catalyst with 0.1 wt.% loading, the types of carbon resulting from cracking were the same on both promoted and non-promoted catalysts. Higher Mo loaded catalysts (0.3 and 0.5 wt.%) showed higher H₂ yields than the non-promoted catalysts, but lower feed-fuel conversions. XRD revealed that the loss in activity was due to oxidation of active Ni species to inactive Ni and Ni–Mo.