1,721,288 research outputs found
Development of new vanadium-based oxide catalysts for decomposition of chlorinated aromatic pollutants
Supported transition metal oxides and vanadium-containing multi-metallic oxides were investigated to develop new catalysts for the catalytic destruction of highly toxic polychlorinated aromatic pollutants such as polychlorinated benzenes, polychlorinated dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and/or biphenyls (PCBs) from waste gases. The decomposition of 1,2-dichlorobenzene (Cl(2)Bz) was chosen as a model reaction. Titanic-supported vanadium catalyst (VOx/TiO2) showed the highest activity and stability among the binary oxides tested even in the presence of water vapor. The optimum loading of vanadia was 5 wt %, corresponding to half a monolayer, suggesting that the active species are tetrahedral vanadyl species on titanic. Characterizations of the VOx/TiO2 catalysts were carried out with XRD, laser Roman spectroscopy, and TPR. Multi-metallic VOx/TiO2 catalysts prepared by incorporating Mo, W, or Cr showed enhanced activities for Cl(2)Bz oxidation. Among the tested catalysts, V-Mo-O-x/TiO2 catalysts wash-coated on the cordierite honeycomb showed a good activity for the decomposition of the toxic PCDDs/PCDFs in the flue gas emitted from a municipal solid waste incinerator (MSWI)
Hierarchical reduction and partition of hypergraph
In this paper, a hierarchical reduction method of hypergraphs is proposed. A macro-vertex in a reduced hypergraph corresponds to an edge of the original hypergraph, and thus a reduced hypergraph can provide a partition of a system. The reduction is realized by the iterations and the sequence of hierarchical reduction gives a sequence of hierarchical partitions. The proposed method allows to reduce and decompose the complexity of the system represented by hypergraphs
Interference-based channel assignment for DS-CDMA cellular systems
Link capacity is defined as the number of channels available in a link, In direct-sequence code-division multiple-access (DS-CDMA) cellular systems, this is limited by the interference present in the link. The interference is affected by many environmental factors, and, thus, the link capacity of the systems varies with the environment. Due to the varying link capacity, static channel assignment (SCA) based on fixed link capacity is not fully using the link capacity. This paper proposes a more efficient channel assignment based on the interference received at the base station (BS), In the proposed algorithm, a channel is assigned if the corresponding interference margin is less than the allowed interference, and, thus, channels are assigned adaptively to dynamically varying link capacity, Using the proposed algorithm yields more channels than using SCA in such an environment changes with nonhomogeneous traffic load or varying radio path loss, The algorithm also improves service grade by reserving channels for handoff calls
Photocatalytic activity of monodispersed spherical TiO2 particles with different crystallization routes
Monodispersed spherical TiO2 particles were prepared by hydrothermal crystallization and/or calcination of spherical amorphous particles, synthesized by thermal hydrolysis of TiCl4. The crystallized spherical particles were secondary agglomerates of primary nanocrystallites. Different crystallization routes and conditions provided the spherical TiO2 particles with wide particle characteristics, such as the fraction of crystallization, the size and shape of the primary nanocrystallites, and the specific surface area. The photocatalytic activity showed complex dependence on the crystallization routes and conditions. The complex dependence behavior could be explained by combining the effects of the fraction of crystallization, the specific surface area, and the adsorption ability for hydroxyl ions. Especially, in the present study, the hydrothermally crystallized TiO2 particles with large primary nanocrystallites showed the highest photocatalytic activity. The high photocatalytic activity mainly resulted from the high surface adsorption ability for hydroxyl ions, which was closely related to the well-developed (flat and faceted) morphology of primary nanocrystallite
Dynamics of simple fluids confined in cylindrical pore: Effect of pore size
We study the thermodynamic and dynamical properties of Weeks-Chandler-Anderson (WCA) fluids confined in a cylindrical pore by means of a canonical molecular dynamics simulation method. The pore model is an infinitely long cylinder consisted of a thermal wall and mimics a typical carbon nanotube. The thermodynamic properties axe obtained for relatively high density fluids over a wide range of pore diameters at a given temperature. The size dependence of the self-diffusion coefficients in the cylindrical pore is also investigated. It is found that, as the pore diameter decreases, the potential energy and axial component of the pressure exhibit a sharp rise and the self-diffusion coefficient decreases. The observed behaviors can be understood in terms of the geometrical confinement and attenuation of transport induced by dispersive fluid-wall interaction. In addition, anomalous diffusion is observed at the pore size corresponding to twice the particle diameter
Washing-free all-in-one immunostaining reaction of multi-step quantum dot labeling reagents
Reset level Boosting in Self-adaptive CMOS Active Pixel Sensor for a Wide Output Voltage Swing at Low Voltage Operation
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
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