CH_4 reforming with CO_2 for syngas production over La_2O_3 promoted Ni catalysts supported on mesoporous nanostructured γ-Al_2O_3

Nanostructured γ-Al2O3 with high surface area and mesoporous structure was synthesized by sol-gel method and employed as catalyst support for nickel catalysts in methane reforming with carbon dioxide. The prepared samples were characterized by XRD, N2adsorption-desorption,TPR, TPO, TPH, NH3-TPD and SEM techniques. The BET analysis showed a high surface area of 204 m2 g-1and a narrow pore-size distribution centered at a diameter of 5.5 nm for catalyst support. The BET results revealed that addition of lanthanum oxide to aluminum oxide decreased the specific surface area. In addition, TPR results showed that addition of lanthanum oxide increased the reducibility of nickel catalyst. The catalytic evaluation results showed an increase in methane conversion with increasing lanthanum oxide to 3 mol% and further increase in lanthanum content decreased the catalytic activity. TPO analysis revealed that the coke deposition decreased with increasing lanthanum oxide to 3 mol%. SEM and TPH analyses confirmed the formation of whisker type carbon over the spent catalysts. Addition of steam and O2 to dry reforming feed increased the methane conversion and led to carbon free operation in combined processes.     

Synthesis of Polymer Nanoparticles in the Presence of Diatoms as Sustainable Bio-Templates

Colloid Journal - Preparation of complex nano- and micron-sized non-spherical particulate geometries still remains a challenge. One potential approach is the utilization of natural templates with...     

CH4 reforming with CO2 for syngas production over La2O3 promoted Ni catalysts supported on mesoporous nanostructured γ-A12O3

Nanostructured -y-A12O3 with high surface area and mesoporous structure was synthesized by sol-gel method and employed as catalyst support for nickel catalysts in methane reforming with carbon dioxide. The prepared samples were characterized by XRD, N2 adsorption-desorption, TPR, TPO, TPH, NH3-TPD and SEM techniques. The BET analysis showed a high surface area of 204 m2.g-1 and a narrow pore-size distribution centered at a diameter of 5.5 nm for catalyst support. The BET results revealed that addition of lanthanum oxide to aluminum oxide decreased the specific surface area. In addition, TPR results showed that addition of lanthanum oxide increased the reducibility of nickel catalyst. The catalytic evaluation results showed an increase in methane conversion with increasing lanthanum oxide to 3 mol% and further increase in lanthanum content decreased the catalytic activity. TPO analysis revealed that the coke deposition decreased with increasing lanthanum oxide to 3 mol%. SEM and TPH analyses confirmed the formation of whisker type carbon over the spent catalysts. Addition of steam and Oxide to drv reformin feed increased the methane conversion and led to carbon free ooeration in combined orocesses.     

Collision problems of random walks in two-dimensional time

The collision problems of two-parameter random walks are studied. That is, some criteria have been established in terms of the characteristic functions of two or more mutually independent random walks in order to determine if they meet infinitly often in certain restricted time sets.     

Kinetics Study of the Thermal Decomposition of Post-consumer Poly(Ethylene Terephthalate) in an Argon Atmosphere

The thermal decomposition of post-consumer samples of a carbonated water bottle made of poly(ethylene terephthalate), PC-PET, was examined by linear temperature programing under an argon atmosphere to determine its mass loss kinetics. A simple kinetic model, called the first order pseudo single-component model, was used. The total weight-loss of each sample assumed to be in two periods, with each period corresponding to a one step decomposition of the PC-PET to volatiles. Three methods for determining the kinetic parameters by thermal gravimetric analysis were examined: differential analysis at a constant heating rate (differential), temperatures of a given conversion at a number of heating rates (isoconversional), and the maximum rate at multiple heating rates (peak temperature). The latter two multiple heating rates methods results were comparable to each other but they were not in agreement with the results from the differential method. The results of the differential method were insensitive to the heating rate and consistent with kinetics data reported in the literature for PET.     

Monitoring the effects of homogeneity methanol/water/monomer on the mode of polymerization of styrene: dispersion polymerization versus emulsion polymerization

The polymerization of styrene (St) was carried out with varying amounts of methanol in aqueous medium. As methanol content decreased (to 50 %), the phase of polymerization mixture (methanol/water/monomer) changed to a heterogeneous state; the homogeneous state was obtained in samples that contain 75 and 100 % methanol. In order to verify the mechanism of polymerization in heterogeneous and homogeneous mixtures, the nucleus formation rate during polymerization, the stability equilibrium of the media and seeded particles, and the size of particles and their growth in polymerization were experimentally being monitored. With the homogeneous mixture in 75 wt% methanol, dumbbell, triangle, and peanut-like particles have been formed. On the other hand, the characteristics of the polymerization products were different from those typically obtained in the emulsion polymerization and in the sample with 100 wt% methanol dispersion polymerization. In the sample with 100 % methanol and in one with 50 % methanol, monodispersed spherical particles are formed in the final conversion. Thus, homogeneity in the aqueous methanol mixture can be a critical factor in determining the polymerization modes between dispersion and emulsion polymerization.     

Thermally driven sensitive surface phonon polariton modes in thin-film SiC

The results of this work show that significant changes to the spectral properties of thermal emission may be accomplished by taking advantage of surface phonon polariton (SPP) modes that are very sensitive to small refractive index changes. Surface phonon polaritons are interface restricted wave modes that do not usually participate in thermal radiative energy exchange. In this work, the possibility of varying the spectral properties by using a thin-film surface active material, layered between dielectrics, is explored. Unlike surface gratings, the multilayered structure discussed in this work couples the surface modes into radiative modes using subtle changes in refractive index. The proposed multilayer effect is studied by first developing the SPP mode dispersion relation to identify the spectral location of the surface modes. The relationship between SPP coupling and refractive index change is then developed. The fluctuation-dissipation theorem and an impedance boundary condition is used to theoretically show how thermal radiation can excite SPP modes. Results are then presented that show how film thickness and substrate properties act to support SPP modes that are particularly sensitive to changes in refractive index and therefore offers opportunities for dramatic changes to the spectral properties.     

Optimization strategies for radiation induced grafting of 4-vinylpyridine onto poly(ethylene-co-tetraflouroethene) film using Box-Behnken design

The radiation induced grafting of 4-vinylpyridine (4-VP) onto poly(ethylene-co-tetrafluoroethene) (ETFE) was optimized using the Box-Behnken factorial design available in the response surface method (RSM). The optimized grafting parameters; absorbed dose, monomer concentration, grafting time and reaction temperature were varied in four levels to quantify their effect on the grafting yield (GY). The validity of the statistical model was supported by the small deviation between the predicted (GY=61%) and experimental (GY=57%) values. The optimum conditions for enhancing GY were determined at the following values: monomer concentration of 48 vol%, absorbed dose of 64 kGy, reaction time of 4 h and temperature of 68 °C. A comparison was made between the optimization model developed for the present grafting system and that for grafting of 1-vinylimidazole (1-VIm) onto ETFE to confirm the validly and reliability of the Box-Behnken for the optimization of various radiation induced grafting reactions. Fourier transform infrared (FTIR), thermogravimetric analysis (TGA) and X-ray diffraction (XRD) were used to investigate the properties of the obtained films and provide evidence for grafting.