Made available in DSpace on 2017-07-10T17:37:50Z (GMT). No. of bitstreams: 1 Loana Bergamo dos Santos.pdf: 1109658 bytes, checksum: 86a9ba08470cd16b7befaff7cd272ca6 (MD5) Previous issue date: 2011-03-30 / The constant search for sustainability of production systems have driven research to find alternatives to the problems arising from the intensification of production systems. In this context the present work was to study the effects of substitution of mineral nitrogen by chicken litter in oat and corn in succession and chemical characteristics of soil. Two experiments were conducted during the period from May 2009 to March 2010 in Oxisol area located at the experimental farm of the State University of Paraná, municipality of Rondon. The first test was conducted under a randomized complete blocks with eight treatments obtained from different combinations of chicken manure (applied in oat) and mineral N fertilization (applied in corn) and four replications. We studied the production of dry matter and nutrient accumulation in the straw of the oat crop, and yield components and yield of corn. In the second trial, after the corn harvest, we studied the chemical properties of soil under the design of randomized blocks in factorial scheme 8x3, with the eight combinations of fertilizer used in the first trial related to three depths of soil sampling (0 -5, 5-10 and 10-15 cm). Larger quantities of poultry litter in oat provided higher dry matter production and accumulation of N. All fertilization studied provided satisfactory average productivity for corn (8569 kg ha-1). The soil properties were changed with the use of poultry litter associated with mineral N fertilization. There was a decrease in pH, Ca, Mg, and increased the P, potential acidity, the cation exchange capacity and exchangeable Al with increasing proportions of poultry litter in relation to mineral N fertilization / A busca constante pela sustentabilidade dos sistemas de produção têm direcionado as pesquisas à buscar alternativas aos problemas oriundos da intensificação dos sistemas produtivos. Nesse contexto o presente trabalho teve como objetivo estudar os efeitos da substituição da adubação nitrogenada mineral pela cama de frango na cultura da aveia e do milho em sucessão e nos atributos químicos do solo. Foram conduzidos dois ensaios durante o período de maio de 2009 à março de 2010 em área de Latossolo Vermelho eutroférrico localizada na fazenda experimental da Universidade Estadual do Oeste do Paraná, município de Marechal Cândido Rondon. O primeiro ensaio foi conduzido sob o delineamento em blocos ao acaso com seis tratamentos obtidos a partir de combinações de quantidades crescentes de cama de frango aplicadas na aveia combinadas com a adubação nitrogenada mineral de cobertura aplicada no milho e quatro repetições. Estudou-se a produção de massa seca e acúmulo de nitrogênio pela cultura da aveia, e os componentes de produção e produtividade da cultura do milho. No segundo ensaio, após a colheita do milho, estudou-se os atributos químicos do solo sob o delineamento em blocos ao acaso em esquema fatorial 6X3, com as seis combinações de adubação utilizadas no primeiro ensaio associadas a três profundidades de amostragem do solo (0-5; 5-10 e 10-15 cm). A aplicação de cama de frango na cultura da aveia propiciou aumento da produção de massa seca e acúmulo de maior quantidade de N, enquanto a substituição de parte da adubação nitrogenada mineral pela cama de frango elevou os índices de produtividade da cultura do milho. Os atributos químicos do solo foram alterados pelos fatores estudados, ocorrendo a elevação dos teores de P, MO, Al trocável e acidez potencial, e redução do pH, K, Ca, Mg, soma de bases e saturação por bases.

Radioisótopos de gálio são estudados e avaliados para aplicações médicas desde 1949. Nos últimos 50 anos 67Ga tem sido amplamente utilizado no diagnóstico de diversas patologias, incluindo lesões inflamatórias crônicas e agudas, bacterianas ou estéreis e diversos tipos de tumores. No Brasil 30% das clinicas que prestam serviços de Medicina Nuclear utilizam o Citrato de 67Ga com uma demanda de distribuição no IPEN-CNEN/SP de 37 GBq (1 Ci) por semana. O 67Ga apresenta meia-vida física de 3,26 dias (78 horas) e decai 100% por captura eletrônica para o 67Zn estável. Seu decaimento inclui a emissão de raios γ com energias de 93,3 keV (37%), 184,6 keV (20,4%), 300,2 keV (16,6%) e 888 keV (26%). No IPEN o 67Ga era produzido a partir da reação 68Zn(p, 2n)67Ga. Após a irradiação, o alvo era totalmente dissolvido em HCl concentrado e a solução percolada em resina catiônica DOWEX 50W-X8, 200-400 mesh, condicionada em HCl 10 mol L-1. Zinco, níquel e cobre eram eluídos em HCl 10 mol L-1 e o 67Ga em HCl 3,5 mol L-1. O produto final era obtido na forma de citrato de 67Ga. Este trabalho apresenta um método inédito, rápido, direto e eficiente de separação química e obtenção de 67GaCl3 a partir da difusão térmica (aquecimento do alvo) aliada à extração em ácido acético concentrado. A purificação foi realizada por cromatografia de troca iônica. Realizou-se a eletrodeposição do zinco natural em placas de cobre niquelado como substrato e os depósitos de zinco obtidos foram aderentes ao substrato, levemente brilhantes e uniformes. Os alvos foram irradiados com prótons de 26 MeV e corrente integrada de 10 μA.h. Após a irradiação, os alvos foram aquecidos a 300 °C por 2 horas e colocados em contato com ácido acético concentrado por 1 hora. O rendimento médio de extração de 67Ga obtido foi de (72±10)%. Esta solução foi evaporada e o resíduo foi retomado em NH4OH 0,5 mol L-1. O 67Ga foi purificado em resina catiônica Dowex 50WX8 em meio de NH4OH. A recuperação obtida foi de (98 ± 2) %, de 67Ga. O eluido foi evaporado e retomado em HCl 0,1 mol L-1. A pureza química foi verificada por ICP-OES encontrando-se (2 ± 1) μg mL -1 de zinco. As concentrações de ferro, cobre e níquel foram inferiores ao limite de detecção do método e aos limites de utilização de 67Ga. A pureza radionuclídica foi verificada por espectroscopia-γ utilizando um detector de germânio Hiper-Puro encontrando-se valor superior a (99,9%). Este método inédito permite a obtenção de 67Ga com alta pureza química, radioquímica e radionuclídica em condições de processamento menos agressivas e corrosivas que o método comumente utilizado. / Radioisotopes of gallium have been studied and evaluated for medical applications since 1949. Over the past 50 years 67Ga has been widely used in the diagnosis of various diseases, including acute and chronic inflammatory lesions, bacterial or sterile and several types of tumors. In Brazil 30% of clinics that provide services for Nuclear Medicine use 67Ga citrate and the demand for 67Ga at IPEN-CNEN/SP is 37 GBq (1 Ci)/week. The 67Ga presents physical half-life of 3.26 days (78 hours) and decays 100% by electron capture to stable 67Zn. Its decay includes the emission of γ rays with energies of 93.3 keV (37%), 184.6 keV (20.4%), 300.2 keV (16.6%) and 888 keV (26%). In the past 67Ga was produced by the reaction 68Zn (p, 2n) 67Ga at IPEN-CNEN/SP. After irradiation, the target was dissolved in concentrated HCl and the solution percolated through a cationic resin DOWEX 50W-X8, 200-400 mesh, conditioned with 10 mol L -1 HCl. Zinc, nickel and copper were eluted in 10 mol L-1 HCl and 67Ga 3.5 mol L-1 HCl. The final product was obtained as 67Ga citrate. This work presents a new, fast, direct and efficient method for the chemical separation of 67Ga by thermal diffusion (heating of the target) combined with concentrated acetic acid extraction. Purification was performed by ion exchange chromatography. Natural zinc electrodeposition was performed on nickel/copper plates as substrate and the zinc deposits were adherent to the substrate, slightly shiny and uniform. The targets were irradiated with 26 MeV protons and integrated current of 10 μA.h. After irradiation, the targets were heated at 300 °C for 2 hours and placed in contact with concentrated acetic acid for 1 hour. The average yield of extraction of 67Ga was (72 ± 10)%. This solution was evaporated and the residue was taken up in 0.5 mol L-1 NH4OH. The 67Ga was purified on cationic resin Dowex 50WX8 in NH4OH medium. The 67Ga recovery was (98 ± 2)%. This solution was evaporated and taken up in 0.1 mol L-1 HCl. The chemical purity was evaluated by ICP-OES that resulted in (2 ± 1) μg mL-1 of zinc. The concentration of iron, copper and nickel was lower than the detection limits and also than the utilization limits for 67Ga. The radionuclidic purity was greater than (99.9%). This method showed to be suitable to obtain high purity 67Ga in less aggressive chemical conditions than before.

No description available.

Expansive clay mineral contamination of road aggregate materials in Texas is a persistent problem. Hydrous layer silicate minerals - particularly smectites - in concretes are associated with decreased strength and durability in Portland cement and asphalt concretes. The Texas Department of Transportation (TXDOT) and Texas A&M Transportation Institute (TTI) evaluated the methylene blue adsorption test for its potential to identify and estimate quantities of expansive clays in aggregate stockpiles. Clay mineral quantification was completed for 27 geologically-diverse aggregate materials from Texas, Oklahoma, and Arkansas. X-ray diffraction analysis (XRD) of separated clays on glass was conducted, and NEWMOD was utilized to model the resulting diffraction patterns. Methylene blue adsorption (MBA) and cation exchange capacity (CEC) of clay fractions (< 2µm) and -40 mesh screenings (< 400 µm) were determined for most aggregates. Many of the aggregates exhibited significant quantities of expansive clay minerals such as smectite, which are linked to deleterious performance properties in concretes. While the majority of aggregates were derived from crushed limestone or calcareous river gravel parent materials, severalexhibited uncommon origins and unusual clay mineralogy. Due to the relatively low number of aggregates tested and diverse geological origins of the different aggregates,it proved difficult to formalize any conclusions abouttrendsbetweenthedifferent aggregate performance properties.

No description available.

The use of geosynthetic clay liners (GCLs) as (i) covers for arsenic-rich gold mine tailings and landfills, (ii) subsurface barrier for migration of hydrocarbons in the Arctic, and (iii) basal liner for sewage treatment lagoons were examined. After 4 years in field and laboratory experiments, it was found that best cover configuration above gold mine tailings might include a layer of GCL product with polymer-enhanced bentonite and a geofilm-coated carrier geotextile serving above the tailings under ≥ 0.7 m overburden. However, acceptable performance could be achieved with using a standard GCL with untreated bentonite provided that there is a minimum of 0.7 m of cover soil above the GCL. When GCL samples were exhumed from experimental landfill test cover with complete replacement of sodium in the bentonite with divalent cations in the adjacent soil, it was observed that the (i) hydraulic head across the GCLs, (ii) size of the needle-punched bundles, and (iii) structure of the bentonite can all significantly affect the value of the inferred in-situ hydraulic conductivity measured at the laboratory. The higher the hydraulic head and the larger the size of the needle-punched bundles, the higher the likelihood of internal erosion/structural change of bentonite at bundles that will cause a preferential flow for liquids to occur. A key practical implication was that GCLs can perform effectively as a single hydraulic barrier in covers provided that the water head above the GCL kept low. The hydraulic performance of a GCL in the Arctic was most affected by the location within the soil profile relative to the typical groundwater level with the highest increase in the hydraulic conductivity (by 1-4 orders of magnitude) for GCL below the water table. However, because the head required for jet fuel to pass through the GCL was higher than that present under field conditions, there was no evidence of jet fuel leakage through the barrier system. The leakage through GCLs below concrete lined sewage treatment lagoons was within acceptable limits, in large part, due to the low interface transmissivity between GCLs and the overlying poured concrete. / Thesis (Ph.D, Civil Engineering) -- Queen's University, 2014-02-28 08:53:29.171

No description available.

LTA-type zeolites with narrow window apertures coinciding with the approximate size of small gaseous molecules such as CO2 and N2 are interesting candidates for adsorbents with swing adsorption technologies due to their molecular sieving capabilities and otherwise attractive properties. These sieving capabilities are dependent on the energy barriers of diffusion between the zeolite pores, which can be fine-tuned by altering the framework composition. An ab initio level of theory is necessary to accurately describe specific gas-zeolite interaction and diffusion properties, while it is desirable to predict the macroscopic scale diffusion for industrial applications. Hence, a multiscale modeling approach is necessary to describe the molecular sieving phenomena exhaustively. In this thesis, we use several different modeling methods on different length and time scales to describe the diffusion driven uptake and separation of CO2 and N2 in Zeolite NaKA. A combination of classical force field based modeling methods are used to show the importance of taking into account both thermodynamic, as well as, kinetic effects when modeling gas uptake in narrow pore zeolites where the gas diffusion is to some extent hindered. For a more detailed investigation of the gas molecules’ pore-to-pore dynamics in the material, we present a procedure to compute the free energy barriers of diffusion using spatially constrained ab initio Molecular Dynamics. With this procedure, we seek to identify diffusion rate determining local properties of the Zeolite NaKA pores, including the Na+-to-K+ exchange at different ion sites and the presence of additional CO2 molecules in the pores. This energy barrier information is then used as input for the Kinetic Monte Carlo method, allowing us to simulate and compare these and other effects on the diffusion driven uptake using a realistic powder particle model on macroscopic timescales. / <p>At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 4: Manuscript.</p>

Mechanisms of adsorption of alkaline copper quat (ACQ) components in wood were investigated with emphasis on: copper chemisorption, copper physisorption, and quat adsorption. Various factors were investigated that could affect the adsorption of individual ACQ components in red pine wood. Copper chemisorption in wood was affected by ligand types coordinating with Cu and the stability of the Cu-ligand complexes in solution. For Cu-monoethanolamine (Cu-Mea) system, the prevailing active solvent species at the solution pH, [Cu(Mea)2-H]+ complexes with wood acid sites and loses one Mea molecule through a ligand exchange reaction. The amount of adsorbed Cu was closely related to the cation exchange capacity of wood. An increase in Mea/Cu ratio increased the proportion of the uncharged Cu-Mea complex and resulted in decreased Cu chemisorption in wood. Copper precipitation is also an important Cu fixation mechanisms of Cu-amine treated wood. X-ray diffraction analysis revealed that in vitro precipitated Cu was a mixture of copper carbonates (azurite and malachite) and possibly Cu2O. Higher concentration Cu-amine solutions retarded the Cu precipitation to a lower pH because of higher free amine in the preservative-wood system. The changes in zeta potential of wood in relationship to the quaternary ammonium (alkyldimethylbenzylammonium chloride: ADBAC) adsorption isotherm showed two different adsorption mechanisms for quat in wood: ion exchange reaction at low concentration and additional aggregation form of adsorption by hydrophobic interaction at high concentration. Because of the aggregation effect, when wood was treated with ACQ, high amounts of ADBAC were concentrated near the surface creating a steep gradient with depth. This aggregated ADBAC was easily leached out while the ion exchanged ADBAC had high leaching resistance. Free Mea and Cu of ACQ components appeared to compete with ADBAC for the same bonding sites in wood.

This study focuses on the entire proces of composting. It begins with listing the attributes of entry materials and spans to outlining the creation of characteristic substances in the compost (humus). Problems and solutions relating to determining the quality and quantity of humus in the compost are elaborated. This thesis was designed to identify efficient compost accelerator additives for gardening composts.