781,744 research outputs found
Energy conversion in isothermal nonlinear irreversible processes - struggling for higher efficiency
First we discuss some early work of Ulrike Feudel on structure formation in
nonlinear reactions including ions and the efficiency of the conversion of
chemical into electrical energy. Then we give some survey about energy
conversion from chemical to higher forms of energy like mechanical, electrical
and ecological energy. We consider examples of energy conversion in several
natural processes and in some devices like fuel cells. Further, as an example,
we study analytically the dynamics and efficiency of a simple "active circuit"
converting chemical into electrical energy and driving currents which is
roughly modeling fuel cells. Finally we investigate an analogous ecological
system of Lotka - Volterra type consisting of an "active species" consuming
some passive "chemical food". We show analytically for both these models that
the efficiency increases with the load, reaches values higher then 50 percent
in a narrow regime of optimal load and goes beyond some maximal load abrupt to
zero.Comment: 25 pages, 4 figure
Chemistry in Evaporating Ices: Unexplored Territory
We suggest that three-body chemistry may occur in warm high density gas
evaporating in transient co\textendash desorption events on interstellar ices.
Using a highly idealised computational model we explore the chemical conversion
from simple species of the ice to more complex species containing several heavy
atoms, as a function of density and of adopted three body rate coefficients. We
predict that there is a wide range of densities and rate coefficients in which
a significant chemical conversion may occur. We discuss the implications of
this idea for the astrochemistry of hot cores.Comment: Accepted in Ap
Coannihilation without chemical equilibrium
Chemical equilibrium is a commonly made assumption in the freeze-out
calculation of coannihilating dark matter. We explore the possible failure of
this assumption and find a new conversion-driven freeze-out mechanism.
Considering a representative simplified model inspired by supersymmetry with a
neutralino- and sbottom-like particle we find regions in parameter space with
very small couplings accommodating the measured relic density. In this region
freeze-out takes place out of chemical equilibrium and dark matter
self-annihilation is thoroughly inefficient. The relic density is governed
primarily by the size of the conversion terms in the Boltzmann equations. Due
to the small dark matter coupling the parameter region is immune to direct
detection but predicts an interesting signature of disappearing tracks or
displaced vertices at the LHC. Unlike freeze-in or superWIMP scenarios,
conversion-driven freeze-out is not sensitive to the initial conditions at the
end of reheating.Comment: 12 pages + references, 10 figures; v2: Discussion of kinetic
equilibrium extended, matches published versio
Modelling of an industrial moving belt chemical vapour deposition reactor forming SiO2 films
In order to improve the efficiency of an industrial atmospheric pressure chemical vapour deposition (APCVD) moving belt reactor depositing silicon dioxide SiO2 films from tetraethoxysilane Si(OC2H5)4 (TEOS) andozone O3, a 2D simulation model based on the computational fluid dynamics (CFD) software ESTET has been developed. On the basis of the global chemical scheme of Zhou et al. [1997. Fifth International Conference on Advanced Thermal Processing of Semiconductors, RTPâ97, New Orleans, LA, USA, pp. 257â268], a new kinetic model has been developed to conveniently represent our own set of experimental data. In particular, a chemical limitation for TEOS has been introduced, conferring increased chemical validity to the model. Simulations have shown that for the nominal conditions, TEOS conversion into SiO2 layers was too low andthat an increase in ozone concentration or in the nitrogen flow rates through the injector did not offer any advantage. Conversely, a decrease in the curtain nitrogen flow rate or an increase in that of the shieldcan enhance the process productivity and TEOS conversion
Segregation by Race in Public Schools Retrospect and Prospect
Solar energy conversion has been intensively studied in past decades and has been shown to be greatly effective for solving the serious environmental pollution and energy shortage problems. Photoelectrocatalysis and photovoltaics have been considered as the two main approaches for solar energy conversion and utilization, which are generally involved with nanostructured materials and/or catalytic processes, greatly affecting the efficiencies for solar energy conversion. Then, it is necessary to understand the relationship between the physical and chemical properties of nanomaterials and their performances for solar energy conversion. It is also important to explore the fundamentals in catalytic processes for solar energy conversion and make breakthrough in design and synthesis of nanomaterials or nanostructures, characterization of material properties, and performance of novel devices and systems. The aim of this special issue is to present some recent progress in the field of advanced catalysis and nanostructure design for solar energy conversion. A brief summary of all accepted papers is provided below
Utilizing Imogolite Nanotubes as a Tunable Catalytic Material for the Selective Isomerization of Glucose to Fructose
The isomerization of glucose to fructose is an important step in the conversion of biomass to valuable fuels and chemicals. A key challenge for the isomerization reaction is achieving high selectivity towards fructose using recyclable and inexpensive catalysts. Imogolite is a single-walled aluminosilicate nanotube characterized by surface areas of 200-400 m2/g and pore widths near 1 nm. In this study, imogolite nanotubes are used as a heterogeneous catalyst for the isomerization of glucose to fructose. Catalytic testing demonstrates the catalytic activity of imogolite for the isomerization of glucose to fructose. Imogolite is a highly tunable structure and can be modified through substitution of Si with Ge or through functionalization of methyl groups to the inner surface. These modifications change the surface properties of the nanotubes and enable tuning of the catalytic performance. Aluminosilicate imogolite is the most active material for the conversion of glucose. Conversion of glucose of 30% and selectivity for fructose of 45% is achieved using aluminosilicate imogolite. Modification of imogolite with germanium or methyl groups decreases the conversion, but increases the selectivity. Generally, the selectivity for fructose decreases as the conversion of glucose increases. Interestingly, the imogolite nanotubes have comparable catalytic selectivity at similar conversion as base catalyzed reactions. Catalyst recycling experiments revealed that organic content accumulates on the nanotubes that results in a minor reduction in conversion while maintaining similar catalytic selectivity. Overall, imogolite nanotubes demonstrate an active and tunable catalytic platform for the isomerization of glucose to fructose.American Chemical Society Petroleum Research Fund (ACS-PRF 55946-DNI5)National Science Foundation (NSF CBET 1605037; 1653587 and NSF CBET REU 1645126)Ohio State University Institute of Materials Research (OSU IMR FG0138)The Undergraduate Research Office and Office of ResearchA one-year embargo was granted for this item.Academic Major: Chemical Engineerin
Analytical solutions for non-linear conversion of a porous solid particle in a gasâII. Non-isothermal conversion and numerical verification
In Part I, analytical solutions were given for the non-linear isothermal heterogeneous conversion of a porous solid particle. Account was taken of a reaction rate of general order with respect to the gas reactant, intrinsic reaction surface area and effective pore diffusion, which change with solid conversion and external film transport. In this part, the analytical solutions are extended to non-isothermal conversion. Analytical solutions for the particle overshoot temperature due to heat of reaction are derived from the governing differential equation pertaining to conservation of energy, considering the limiting cases of small and large Thiele moduli. The solutions are used to assess the effect of interaction between chemical reaction rate and particle overshoot temperature on particle conversion. The analytical solutions are shown to compare favourably with numerical simulation results
Investigation of electrochemistry of high energy compounds in organic electrolytes, november 1, 1964 - april 30, 1965
Conversion by electrochemical process of chemical to electrical energy - high energy compounds in organic electrolytes and cathode material
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