691 resultados para Carbó activat
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Attempts to reduce the energy consumed in UK homes have met with limited success. One reason for this is a lack of understanding of how people interact with domestic technology – heating systems, lights, electrical equipment and so forth. Attaining such an understanding is hampered by a chronic shortage of detailed energy use data matched to descriptions of the house, the occupants, the internal conditions and the installed services and appliances. Without such information it is impossible to produce transparent and valid models for understanding and predicting energy use. The Carbon Reduction in Buildings (CaRB) consortium of five UK universities plans to develop socio-technical models of energy use, underpinned by a flow of data from a longitudinal monitoring campaign involving several hundred UK homes. This paper outlines the models proposed, the preliminary monitoring work and the structure of the proposed longitudinal study.
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An experiment was conducted to investigate the effects of increasing the level of two sources of fibrous by-products, orange pulp (OP) and carob meal (CM), in iso-NDF growing-finishing pig diets on nutrient balance, slurry composition and potential ammonia (NH3) and methane (CH4) emissions. Thirty pigs (85.4 ± 12.3 kg) were fed five iso-nutritive diets: a commercial control wheat/barley (C) and four experimental diets including two sources of fibrous by-products (OP and CM) and two dietary levels (75 and 150 g/kg) in a 2 × 2 factorial arrangement. After a 14-day adaptation period, faeces and urine were collected separately for 7 days to measure nutrient digestibility and the excretory patterns of N from pigs (6 replicates per diet) housed individually in metabolic pens. For each animal, the derived NH3 and CH4 emissions were measured in samples of slurry over an 11- and 100-day storage periods, respectively. Source and level of the fibrous by-products affected digestion efficiency in a different way as the coefficients of total tract apparent digestibility (CTTAD) for dry matter (DM), organic matter (OM), fibre fractions and gross energy increased with OP but decreased with CM (P < 0.05). Crude protein CTTAD decreased with the inclusion of both sources of fibre, being lower at the highest dietary level. Faecal concentration of fibre fractions increased (P < 0.05) with the level of inclusion of CM but decreased with that of OP (P < 0.01). High dietary level for both sources of fibre increased (P < 0.02) CP faecal content but urine N content decreased (from 205 to 168 g/kg DM, P < 0.05) in all the fibre-supplemented compared to C diet. Additionally, the proportions of undigested dietary, water soluble, and bacterial and endogenous debris of faecal N excretion were not affected by treatments. The initial slurry characteristics did not differ among different fibre sources and dietary levels, except pH, which decreased at the highest by-product inclusion levels. Ammonia emission per kg of slurry was lower in all the fibre-supplemented diets than in C diet (from 2.44 to 1.81 g, P < 0.05). Additionally, slurries from the highest dietary level of by-products tended (P < 0.06) to emit less NH3 per kg of initial total Kjeldahl N and showed a lower B0, independently of the fibre source. Thus, the fibre sources and their dietary levels affected pig nutrient digestion and composition of urine and faeces, showing potential to decrease NH3 and CH4 emissions at high levels of inclusion, independently of type of fibre.
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Mode of access: Internet.
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Mode of access: Internet.
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Tesis Universidad Central, 1858.
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Thesis (doctoral)--
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El constante deterioro de las fuentes h?dricas y su uso como recurso en el abastecimiento de agua para consumo humano han conllevado a la b?squeda de la optimizaci?n de los procesos de tratamiento de forma tal que se alcancen condiciones de agua segura con el menor riesgo posible de afectaciones a la salud de la poblaci?n. Es por esto que los sistemas de abastecimiento de agua potable han adoptado estrategias enmarcadas dentro de los planes de seguridad del agua mediante la reducci?n de la contaminaci?n en la fuente de abastecimiento, la remoci?n o reducci?n de diferentes contaminantes mediante los procesos de tratamiento y la prevenci?n de la contaminaci?n del agua en el sistema de almacenamiento y distribuci?n al usuario final. Al observar que la filtraci?n es una de las etapas m?s cr?ticas dentro del tratamiento por ser la ?ltima barrera f?sica para la remoci?n de part?culas presentes en el agua; se plante? este proyecto de grado para estudiar a escala de laboratorio el uso de carb?n activado granular en el proceso de filtraci?n de agua clarificada del Rio Cauca, con el fin de analizar la eficiencia de remoci?n de turbiedad y materia org?nica medida como UV254 y as? establecer el alcance de los valores l?mite recomendados por las entidades internacionales para la disminuci?n del riesgo microbiol?gico y el riesgo cr?nico que pueda estar asociado a la presencia de materia org?nica en el agua para consumo humano. Se emple? carb?n activado granular de origen bituminoso y arena en seis diferentes configuraciones como medio filtrante principal en la etapa de filtraci?n (50%CAG ? 50% Arena, 65% CAG ? 35% Arena, 75% CAG ? 25% Arena, 85% CAG ? 15% Arena, 90% CAG ? 10% Arena y 100% CAG). Se consider? adem?s una configuraci?n con antracita y arena (70% Antracita ? 30% Arena) para comparar el comportamiento de ambos materiales filtrantes en el tratamiento de agua resultante del proceso de clarificaci?n efectuado por la Planta de Tratamiento de Agua Potable Puerto Mallarino en la ciudad de Cali. Se emple? un sistema de filtraci?n en columnas con distribuci?n de agua mediante conducciones reguladas a un caudal constante de 12 mL/min. El efluente de cada unidad de filtros fue evaluado y comparado con el afluente mediante la medici?n de Color Aparente, Turbiedad, UV254, pH y Conductividad. Se obtuvo como resultado que la configuraci?n C5 con 90% de CAG y 10% Arena logr? una mayor estabilidad de la turbiedad obteniendo valores m?nimos por debajo de 2 UNT (MAVDT), 0.5 UNT (WHO) y 0.15 UNT (EPA) y aunque no tuvo diferencias significativas comparado con el filtro de Antracita y Arena, si present? un mejor desempe?o en la remoci?n de turbiedad debido al alcance de un mayor n?mero de datos por debajo de 0.3 UNT. En cuanto a la eficiencia de remoci?n de materia org?nica en el agua medida como UV254 se observaron mejores resultados para la configuraci?n C4 con 85% de CAG y 15% Arena y aunque las eficiencias de remoci?n de materia org?nica no fueron significativamente altas se observa claramente la ventaja que presenta el uso de CAG como medio filtrante adsorbente comparado con el medio convencional de Antracita y Arena. La obtenci?n de bajas eficiencias de remoci?n fue debido al contenido de material en suspensi?n ya que los filtros de CAG trabajaron en la retenci?n de dicho material afectando considerablemente la capacidad de adsorci?n. Mediante esta investigaci?n se comprob? que la selecci?n adecuada de las condiciones operacionales de los filtros de CAG puede generar agua comparativamente similar o superior a los filtros conformados con materiales convencionales como Antracita y arena. De igual forma, el uso de CAG como medio filtrante para el tratamiento de agua del Rio Cauca es un insumo que puede aportar a una posible estrategia para disminuir el riesgo microbiol?gico y el riesgo cr?nico asociado con el contenido de materia org?nica en el agua distribuida a la poblaci?n cale?a
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La presente propuesta educativa, propone y dise?a una cartilla que informa y educa a la comunidad educativa acerca de la problem?tica de extracci?n minera de carb?n presente en el rio Mel?ndez. Con esto se pretende evidenciar la situaci?n, con el fin de que se reconozcan los graves da?os que estas pr?cticas ocasionan no solo a nivel ambiental sino tambi?n social. Este trabajo se enmarca en una metodolog?a cualitativa, presentada en dos fases, que finalizando permitieron la creaci?n de una cartilla educativa que responde a todos los objetivos y planteamientos realizados en el presente trabajo.
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Disertación presentada en la Facultad de Ciencias y Tecnología de la Universidad Nueva de Lisboa para obtención del grado de Master en Conservación y Restauración (Área de Cerámica)
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A Work Project, presented as part of the requirements for the Award of a Masters Degree in Management from the NOVA – School of Business and Economics
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The manipulation of electric ordering with applied magnetic fields has been realized on magnetoelectric (ME) materials, however, their ME switching is often accompanied by significant hysteresis and coercivity that represents, for some applications, a severe weakness. To overcome this obstacle, this work focus on the development of a new type of ME polymer nanocomposites that exhibits tailored ME response at room temperature. The multiferroic nanocomposites are based on three different ferrite nanoparticles, Zn0.2Mn0.8Fe2O4 (ZMFO), CoFe2O4 (CFO) and Fe3O4 (FO), dispersed in a piezoelectric co-polymer poly(vinylindene fluoride-trifluoroethylene), P(VDF-TrFE), matrix. No substantial differences were detected on the time-stable piezoelectric response of the composites (≈ -28 pC.N−1) with distinct ferrite fillers and for the same ferrite content of 10wt.%. Magnetic hysteresis loops from pure ferrite nanopowders showed different magnetic responses. ME results of the nanocomposite films with 10wt.% ferrite content revealed that the ME induced voltage increases with increasing DC magnetic field until a maximum of 6.5 mV∙cm−1∙Oe−1, at an optimum magnetic field of 0.26 T, and 0.8 mV∙cm−1∙Oe−1, at an optimum magnetic field of 0.15T, for the CFO/P(VDF-TrFE) and FO/P(VDF-TrFE) composites, respectively. On the contrary, the ME response of the ZMFO/P(VDF-TrFE) exposed no hysteresis and high dependence on the ZMFO filler content. Possible innovative applications such as memories and information storage, signal processing, ME sensors and oscillators have been addressed for such ferrite/PVDF nanocomposites.
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A series of colloidal MxFe3-xO4 (M = Mn, Co, Ni; x = 0–1) nanoparticles with diameters ranging from 6.8 to 11.6 nm was synthesized by hydrothermal reaction in aqueous medium at low temperature (200 °C). Energy-dispersive X-ray microa-nalysis and inductively coupled plasma spectrometry confirms that the actual elemental compositions agree well with the nominal ones. The structural properties of obtained nanoparticles were investigated by using powder X-ray diffraction, Raman scattering, Mössbauer spectroscopy, and electron microscopy. The results demonstrate that our synthesis technique leads to the formation of chemically uniform single-phase solid solution nanoparticles with cubic spinel structure, confirming the intrinsic doping. Magnetic studies showed that, in comparison to Fe3O4, the saturation magnetization of MxFe3-xO4 (M = Mn, Ni) decreases with increasing dopant concentration, while Co-doped samples showed similar saturation magnetizations. On other hand, whereas Mn- and Ni-doped nanoparticles exhibits superparamagnetic behavior at room temperature, ferromagnetism emerges for CoxFe3-xO4 nanoparticles, which can be tuned by the level of Co doping.