40 research outputs found
Is Semantic Vigilance Impaired by Narrative Memory Demands? Theory and Applications
OBJECTIVE: Two verbal tasks were utilized in a dual-task paradigm to explore
performance theories and prior dual-tasking results.
BACKGROUND: Both the decline in vigilance performance over time, or vigilance
decrement, and limited dual-tasking ability may be explained by limited mental
resources. Resource theorists would recommend removing task demands to avoid
cognitive overload, while mindlessness theorists may recommend adding engaging
task demands to prevent boredom. Prior research demonstrated interference between
a verbal free recall and semantic vigilance task, but exploring tasks with
greater ecological validity is necessary.
METHOD: A narrative memory task and semantic vigilance task were performed
individually and simultaneously. Relative performance impairments were compared
to a previous dual-task pairing.
RESULTS: The semantic vigilance task caused performance degradation to the
narrative memory task and vice versa. A vigilance decrement was not observed, and
the interference was to a lesser extent than when the semantic vigilance task was
paired with a free recall task.
CONCLUSION: Resource theory was supported, though passive learning effects during
a semantic vigilance task with novel stimuli may prevent a vigilance decrement.
The interference was less than that of a previous similar dual-task pairing, but
even tasks as routine as listening to a conversation or story can impair other
task performance.
APPLICATION: A better understanding of resource theory and dual-task performance
outcomes can help inform feasible task loads and improve efficiency and safety of
operators in high-risk and other professions
Desarrollo de catalizadores tiorresistentes para el acoplamiento de tecnologías deNOX en motorización diesel
En las últimas décadas, se han desarrollado y perfeccionado diferentes estrategias y tecnologías deNOx de elevada
eficacia en respuesta a las regulaciones cada vez más estrictas de las emisiones en el sector del automóvil. Dos
tecnologías catalíticas ampliamente utilizadas para este propósito son el Almacenamiento y Reducción de NOx (NSR)
y la Reducción Catalítica Selectiva (SCR) en motorización diésel. El acoplamiento entre una trampa de NOx seguido
de un catalizador NH3-SCR conduce a una mejora de la selectividad a N2, ya que el NH3 no deseado producido en
el catalizador NSR se almacena y reacciona en el sistema SCR consecutivo, se habla de sistemas híbridos. Debido
a la presencia de soot en los gases de escape o de azufre en los combustibles, es necesaria la búsqueda de
materiales resistentes a este tipo de especies estudiando cómo estos contaminantes afectan a su actividad catalítica,
en este sentido, el estudio de la tiorresistencia resulta clave en la determinación de una adecuada formulación del
sistema híbrido catalítico, atendiendo a las condiciones reales de operación.
El objetivo del presente estudio ha sido el desarrollo y mejora de un sistema catalítico híbrido, NSR-SCR, en forma
de monolito, a partir de una formulación base.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech
Reversible and irreversible deactivation of Cu-CHA NH<sub>3</sub>-SCR catalysts by SO<sub>2</sub> and SO<sub>3</sub>
Waste into Fuel—Catalyst and Process Development for MSW Valorisation
The present review paper highlights recent progress in the processing of potential municipal solid waste (MSW) derived fuels. These wastes come from the sieved fraction (∅ < 40 mm), which, after sorting, can differ in biodegradable fraction content ranging from 5–60%. The fuels obtained from these wastes possess volumetric energy densities in the range of 15.6–26.8 MJL−1 and are composed mainly of methanol, ethanol, butanol, and carboxylic acids. Although these waste streams are a cheap and abundant source (and decrease the fraction going to landfills), syngas produced from MSW contains various impurities such as organic compounds, nitrogen oxides, sulfur, and chlorine components. These limit its use for advanced electricity generation especially for heat and power generation units based on high temperature fuel cells such as solid oxide fuel cells (SOFC) or molten carbonate fuel cells (MCFC). In this paper, we review recent research developments in the continuous MSW processing for syngas production specifically concentrating on dry reforming and the catalytic sorbent effects on effluent and process efficiency. A particular emphasis is placed on waste derived biofuels, which are currently a primary candidate for a sustainable biofuel of tomorrow, catalysts/catalytic sorbents with decreased amounts of noble metals, their long term activity, and poison resistance, and novel nano-sorbent materials. In this review, future prospects for waste to fuels or chemicals and the needed research to further process technologies are discussed
Modulating and Orienting an Anisotropic Zn-Based Metal Organic Framework for Selective CH4/CO2 Gas Separation
This work investigates the morphological control of the anisotropic [Zn2(NDC)2(DABCO)]n MOF (Metal organic framework) and the subsequent adsorption characteristics for CO2/CH4 gas separation. Morphology of the MOF crystals is controlled by the use of modulators. The addition of acetic acid or pyridine successfully produce rod or plate morphologies, respectively, with each morphology possessing a different major surface pore aperture. Single-component equilibrium and kinetic adsorption data for CO2 and CH4 were collected. Equilibrium analysis indicates a slight selectivity towards CO2 whereas kinetic data unexpectedly shows lower diffusion time constants for CO2 compared to CH4. Mass transfer resistances on each species is discussed. Finally, a coating technique termed solution shearing is used to orient different morphologies on substrates as a film. An increase in film orientation is observed for the rod morphology, indicating that this MOF morphology is a promising candidate to create large area, thin-film applications
In Situ-DRIFTS Study of Selective Catalytic Reduction of NO<sub><i>x</i></sub> by NH<sub>3</sub> over Cu-Exchanged SAPO-34
The intrinsic mechanism of the selective
catalytic reduction (SCR) reaction over a Cu-exchanged SAPO-34 catalyst
at low temperature was studied by in situ diffuse reflectance infrared
Fourier transform spectroscopy (DRIFTS), coupled with mass spectrometry
to measure inlet and outlet gas concentrations. The evolution of the
surface intermediates, as well as the reactivity of NH<sub>3</sub> with surface NO<sub><i>x</i></sub> species and NO<sub><i>x</i></sub> with surface NH<sub>3</sub> species, was
evaluated. In terms of NO<sub><i>x</i></sub> adsorption,
surface nitrates and nitrites are the main NO<sub><i>x</i></sub> adsorption species at low temperature. When NO was exposed
to the sample with NH<sub>3</sub> preadsorbed, surface NH<sub>3</sub> was not reactive because of the low surface coverage of nitrates
and nitrites. However, the reactivity is significantly enhanced by
the inclusion of O<sub>2</sub> in the feed, which promotes an increase
in the concentration of surface nitrates and nitrites. DRIFTS results
also reveal that the low temperature SCR reaction involves the formation
of an NH<sub>4</sub>NO<sub>3</sub> intermediate and its subsequent
reduction by NO. The NH<sub>4</sub>NO<sub>3</sub> was formed on Lewis
acid sites on the Cu-SAPO-34 sample. The Brønsted acid sites
act as an NH<sub>3</sub> reservoir that supplies additional NH<sub>3</sub> via migration to the Lewis acid sites for the SCR reaction.
The migration of NH<sub>3</sub> between different acid sites was confirmed
in an NH<sub>3</sub>-temperature-programmed desorption (TPD) study.
The presence of NO in the feed reduces surface NH<sub>4</sub>NO<sub>3</sub> to produce N<sub>2</sub> at temperatures as low as 100 °C.
Since NH<sub>4</sub>NO<sub>3</sub> is typically considered an inhibitor,
the onset temperature of the reaction between NO and NH<sub>4</sub>NO<sub>3</sub> is much lower than that reported for other SCR zeolite
catalysts; therefore, it is likely the key factor that results in
the low temperature SCR activity of Cu-SAPO-34