Application of boundary element method to 3-D problems of coupled thermoelasticity

This paper deals with a new boundary element method for analysis of the quasistatic problems in coupled thermoelasticity. Through some mathematical manipulation of the Navier equation in elasticity, the heat conduction equation is transformed into a simpler form, similar to the uncoupled-type equation with the modified thermal conductivity which shows the coupling effects. This procedure enables us to treat the coupled thermoelastic problems as an uncoupled one, A few examples are computed by the proposed BEM, and the results obtained are compared with the analytical ones available in the literature, whereby the accuracy and versatility of the proposed method are demonstrated.     

Thermal Analysis of CNT-Based Nano-Composites by Element Free Galerkin Method

This paper deals with the thermal analysis of carbon nanotube (CNT) based composites by meshless element free Galerkin method. Cylindrical representative volume element (cylindrical RVE) has been chosen to evaluate the thermal properties of nano-composites using multi-domain and simplified approaches. The values of temperature have been calculated at different points and plotted against RVE length and RVE radius. A sensitivity analysis of RVE as well as CNT dimensions has been carried out in detail. The present computations show that the equivalent thermal conductivity is a function of CNT length, CNT radius, RVE length and RVE radius. Based on present numerical simulations, an approximate formula is proposed to calculate the equivalent thermal conductivity of nano-composites. The results obtained by simplified approach have been found in good agreement with those obtained by multi-domain approach.     

Preparation and structural characterization of Co/Al2O3 catalysts for the ozonation of pyruvic acid

A series of Co/Al₂O₃ catalysts were prepared by the incipient wetness impregnation method using γ-Al₂O₃ support and (CH₃COO)₂Co·4H₂O solutions, followed by calcination at 500–800 °C. Characterization of catalysts was accomplished by several techniques such as thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), physisorption of nitrogen, mercury and helium-based pycnometries, Fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and pH of zero charge (PZC). Impregnation of support produced a moderate decrease of its surface area and pore volume and also led to minor changes of its PZC. Depending on preparation conditions (i.e., calcination atmosphere and temperature and metal loading), one or more of the following Co-containing compounds were identified: CoO, Co₃O₄ and CoAl₂O₄. The support and prepared Co/Al₂O₃ catalysts were tested to catalyze the ozonation of aqueous pyruvic acid at pH 2.5. Pyruvic acid was shown refractory towards single ozonation but the use of γ-Al₂O₃ and Co/Al₂O₃ catalysts resulted in 56–96% pyruvic acid conversion and 41–78% decrease in DOC after 2 h of ozonation of phosphate-buffered solutions. In the absence of the buffer, conversion rate was enhanced likely as a result of pH increase during the course of the process thus giving rise to the indirect way of ozonation through hydroxyl radicals. Acetic acid was found as the main by-product of pyruvic acid ozonation. Depending on the catalyst used, yield of acetic acid varied from 32 to 49%, values noticeably lower that that obtained from the control non-catalytic ozonation experiment (73%). Differences in catalytic activity amongst the various Co/Al₂O₃ catalysts investigated were attributed to the different Co active phases deposited on the γ-Al₂O₃ surface. The following sequence of increasing activity can be inferred from experimental results: CoO, CoAl₂O₄ and Co₃O₄. All the Co/Al₂O₃ catalysts prepared showed good stability as the percentage of cobalt leached out was rather low.     

Chemical modification of group IV graphene analogs

Mono-elemental two-dimensional (2D) crystals (graphene, silicene, germanene, stanene, and so on), termed 2D-Xenes, have been brought to the forefront of scientific research. The stability and electronic properties of 2D-Xenes are main challenges in developing practical devices. Therefore, in this review, we focus on 2D free-standing group-IV graphene analogs (graphene quantum dots, silicane, and germanane) and the functionalization of these sheets with organic moieties, which could be handled under ambient conditions. We highlight the present results and future opportunities, functions and applications, and novel device concepts.     

Phenolic resin‐crosslinked natural rubber/clay nanocomposites: Influence of clay loading and interfacial adhesion on strain‐induced crystallization behavior

Nanocomposites of natural rubber (NR) and pristine clay (clay) were prepared by latex mixing, then crosslinked with phenolic resin (PhOH). For comparative study, the PhOH‐crosslinked neat NR was also prepared. Influence of clay loading (i.e., 1, 3, 5, and 10 phr) on mechanical properties and structural change of PhOH‐crosslinked NR/clay nanocomposites was studied through X‐ray diffraction (XRD), transmission electron microscopic (TEM), wide‐angle X‐ray diffraction (WAXD), tensile property measurement, and Fourier transform infrared spectroscopy (FTIR). XRD and TEM showed that the clay was partly intercalated and aggregated, and that the dispersion state of clay was non‐uniform at higher clay loading (>5 phr). From tensile test measurement, it was found that the pronounced upturn of tensile stress was observed when the clay loading was increased and a maximum tensile strength of the PhOH‐crosslinked NR/clay nanocomposites was obtained at 5 phr clay. WAXD observations showed that an increased addition of clay induced more orientation and alignment of NR chains, thereby lowering onset strain of strain‐induced crystallization and promoting crystallinity of the NR matrix during tensile deformation. FTIR investigation indicated a strong interfacial adhesion between NR matrix and clay filler through a phenolic resin bridge. This suggested that the PhOH did not only act as curative agent for crosslinking of NR, but it also worked as coupling agent for promoting interfacial reaction between NR and clay. The presence of strong interfacial adhesion was found to play an important role in the crystallization process, leading to promotion of mechanical properties of the PhOH‐crosslinked NR/clay nanocomposites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43214.     

Homogeneous iron-catalyzed photochemical degradation of muconic acid in water

Iron photochemical oxidation has been used to remove muconic acid from water. Two different light systems were used: black lamps and solar irradiation. The effect of iron concentration, intensity of incident radiation, pH and presence of oxalic acid was investigated. The first two variables yield positive effects on the removal rate of muconic acid while higher efficiency was achieved at pH 3. Oxalic acid enhances the oxidation rate because of the formation of photoactive ferrioxalate ion. Stoichiometric results indicated formation of two hydroxyl radicals to degrade 1 mol of muconic acid. At similar experimental conditions, initial oxidation rates of muconic acid were higher when solar light was used to irradiate the aqueous solutions, although in this case, the oxidation process is stopped because of the consumption of photoactive species.