Navegando por Assunto "Metais de transição"

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Acesso aberto (Open Access)
Adsorção simultânea de íons níquel, zinco e cobre em sedimentos argilosos da Formação Solimões no estado do Acre
(Universidade Federal do Pará, 2011-09-02) CARDOSO, Vivian Mariana Miranda; LEMOS, Vanda Porpino; http://lattes.cnpq.br/1829861620854008
Torrential rains in the Amazon region provide large leaching of micronutrients, which can be controlled from the adsorption reactions of micronutrients in clay minerals. Studies on the geochemical properties of sediment containing high concentrations of clay minerals in the adsorption reactions of micronutrients is a research topic of great importance considering the proven use of clay minerals with a wide range of applications in various processes and procedures adsorption, involving the remediation of sediment, purification of air and water. In order to make contributions on the physical and chemical properties of soils and applicability of the Solimões Formation from Acre State was carried out a study to simulate natural competitive adsorption of micronutrients cobre, níquel e zinco in different adsorbents sites present in these sediment and to evaluate the influence of the attributes mineralogical, chemical and physico-chemical from these adsorption processes. Preliminary data on the mineralogy of soil samples allowed to select four stations distributed among four named as H1RA, H6B, H23A H9F and located along the BR 364 and BR 317, as well as outcrops in the river Acre. Analyses of samples were performed by XRD (using the powder in the range 2θ=o 5-75 ; analysis of clay fraction in sheets oriented air-dried in an atmosphere of ethylene glycol o and heated at 550 ° C (2θ = 3 -35 ) analysis total chemical by ICP-OES; element analysis exchangeable and available to determine parameters of soil fertility. In adsorption experiments the equilibrium concentrations of cobre, níquel and zinco were determined by AAS. We used the models of Langmuir isotherm, Sips, Toth, Temkin Rendlich-Petersen and the fit of the experimental data of adsorption. The results indicated that the samples present as major minerals quartz and clay minerals of the smectite group, mica and kaolinite mineral and the 14th (H6B) preliminarily identified as interstratified mica-chlorite smectite-mica or chlorite-vermiculite. The other minerals identified in the samples were gypsum (H1RA), microcline (H6B and H9F) and albite (H9F). The average chemical composition is represented by 60.99% SiO2, 15.91% Al2O3, 5.84% of Fe2O3, 2.21% K2O, 0.34% of Na2O, 1.26% MgO, 0.86% CaO and 0.86% TiO2. The following ranges were obtained for the parameters of fertility: pHH2O = 5.24 to 8.36; pHKCl = 3.16 to 7.02; CTCefetiva = 3.37 to 25.42 cmol c / kg;% V (base saturation) = 83.08 to 97.63; saturation% Ca = 4.28 to 69.21; saturation% = 11.32 to 76.42 Mg, K saturation% = 2.32 to 17.32;. In the adsorption experiments were obtained the following ranges for the amount of each element adsorbed (mg / g) in soil samples selected: Cu) from 91.30 to 147.46 in H1RA, 47.25 to 83.93 in H6B , 67.13 to 137.36 in H9F; 73.01 to 141.35 in H23A, Ni) from 49.97 to 93.81 in H1RA; 42.51 to 113.44 in H6B; 62.52 to 134.86 in H9F; 54.13 to 172.58 in H23A, Zn) from 50.11 to 104.50 in H1RA, 44.31 to 64.12 in H6B; 60.21 to 89.91 in H9F; 73.84-135 , 60 in H23A. In these experiments was obtained the following values for the initial pH of the aqueous suspensions of samples in H1RA pHinicial=3.88 to 5.38; in pHinicial H6B = 2.71 to 3.27; H9F in pHinicial = 3.16 to 4, 24 and in pHinicial H23A = 2.61 to 3.29. The values of pH equilibrium were 4.38 to 5.2 in the H1RA sample, 2.71 to 3.16 in H6B; 3.24 to 4.2 in H9F; 2.51 to 3.14.in H23A. It was concluded that the sediment samples analyzed have suitable properties adsorptive for simultaneous retention of Cobre, níquel and zinco in water; the samples with montmorilonite (station H23A) and mineral 14A (H6B) present adsorption of metals transition at pH values between 2.5 and 3.1. The samples H1RA H9F with different groups of clay minerals (smectite, kaolinite and mica) the adsorption of transition metals occurs at pH values between 3.2 to 5.5. The ionic strength increases with decreasing pH . The best isotherm models to describe adsorption processes of Cobre, níquel and zinco in sediment samples were the Langmuir and Sips models. The values of ns Sips indicated that the majority of adsorption systems fall between the homogeneous heterogeneous systems. The equilibrium data and thermodynamic processes of simultaneous interaction between these ions and mineral adsorbents indicated that the processes are favorable, spontaneous and the type of adsorption is specific (chemical adsorption) with the formation of inner sphere complexes.
Acesso aberto (Open Access)
Formação de heteroestruturas compostas por microtubos de Cu/Cu2O/CuO decorados com nanocristais de CoO
(Universidade Federal do Pará, 2024-08-21) SANTOS, Suzilene Vasconcelos dos; PASCA, Gabriel Adolfo Cabrera; http://lattes.cnpq.br/5642784995274060; https://orcid.org/0000-0002-9411-0889
A particularly important class of micro/nanostructured materials is that of transition metal oxides. In this work, copper and cobalt oxides are used to obtain micro/nanostructures. Copper (II) oxide (CuO) and copper (I) oxide (Cu2O) are p-type semiconductors, widely studied due to their peculiar characteristics and potential technological applications. Specifically, copper (Cu) microwires with approximately 50 μm in diameter and 4 cm in length, extracted from discarded cellphone earphones, were subjected to thermal treatments at 600°C with different synthesis parameters to obtain CuO microtubes. On the other hand, cobalt acetate was used in the synthesis of nanoparticles through the chemical method called thermal decomposition, which uses organometallic salts in organic solvents, being a suitable method for the synthesis of CoO nanostructures. Metallic cobalt and its oxides have been intensively studied due to numerous applications enhanced by their properties. CoO nanoparticles exhibit instability in the hexagonal close-packed Wurtzite structure (hcp - space group P63mc). This implies that, depending on the synthesis parameters, phase transition can occur, that is, from CoO-hcp to CoO-fcc (face-centered cubic phase - space group Fm3m), which is considered the most stable phase for CoO. However, in order to obtain a hierarchical structure of CuO microtubes decorated with CoO nanoparticles, this work uses different synthesis methodologies to produce a micro-nano-hierarchical structure. In this study, X-ray diffraction was used to identify the crystalline structures present in the microwires and nanoparticles, highlighting the influence of the time parameter on the phase transition of both structures. The morphological characterization of the samples was performed using scanning electron microscopy (for the microwires) and transmission electron microscopy (for the nanoparticles). Raman spectroscopy was also employed to obtain information about the sample surfaces. With these characterization techniques, it was possible to determine the elemental and structural composition of the microtubes and nanoparticles composed of copper and cobalt oxides, as well as to evaluate the influence of the laser on the nanoparticle samples. Thus, a Cu/Cu2O/CuO heterostructure with CoO monocrystals on the surface was developed, presenting potential sensory properties.
Acesso aberto (Open Access)
Fotocatalisadores de dióxido de titânio dopados com metais de transição: síntese, caracterização e aplicação na fotodegradação de fármacos
(Universidade Federal do Pará, 2024-12-27) AZEVEDO, Carla Arnaud de; FARIA, Lênio José Guerreiro de; http://lattes.cnpq.br/7428609361678173
Heterogeneous photocatalysis has shown promise in ecological remediation and in the adequate treatment of pharmaceuticals as emerging contaminants. This study evaluated the photocatalytic activity of materials synthesized from the modification of the TiO₂ surface with transition metals (copper and cobalt) at concentrations of 0.5% and 1.5%, analyzing the physical, chemical and textural properties of the materials by N2 physisorption (BET) analysis, X-ray diffractometry (XRD), scanning electron microscopy–energy-dispersive X-ray spectrometry (SEM-EDS) and Fourier transform infrared (FT-IR). The experimental tests were carried out in an annular photoreactor with UV mercury lamp, following the Box-Behnken design, to evaluate the influence of catalyst mass (50 – 150 mg.L-1 ), drug concentration (2 – 8 mg.L-1 ) and irradiation time (60 – 120 min) on the photodegradation of acetaminophen (ACT) and diclofenac sodium (DCF). The BET results indicated that the materials have a mesoporous structure with an average pore diameter of 14.52 nm. XRD characterization confirmed the mixed structure of anatase and rutile and the absence of metal oxide peaks. The SEM-EDS analysis revealed irregular surfaces formed by misshapen grains and small particles attributed to metal oxides. The FT-IR showed O-H and Ti-O stretching bands, characteristic of photocatalytic materials. The FTCu1.5 photocatalyst was chosen for use in the photodegradation tests of the drugs due to its surface area, porosity and good anatase and copper content. The photocatalysis tests, in comparison with the photolysis tests, showed superior results, evidencing the functionality of the photocatalyst used. The degradation percentages reached 100% for both drugs and the concentration of the pollutant solution had a negative effect on the response variables, indicating that degradation increases with the reduction of the initial concentration of this solution. The proposed polynomial models presented a coefficient of determination (R²) > 0.9 and good predictive capacity. The Response Surface Methodology (RSM) and Desirability Function analyses indicated that it is possible to obtain a substantial reduction in the amount of photocatalyst used, when combined with an adequate adjustment in the irradiation time. The optimal conditions within the experimental domain for ACT are mcat = 100 mg.L-1 , CFA = 2 mg.L-1 and tIRR = 75 minutes, resulting in EffACT(%) = 99.05% and for DCF, the optimal conditions were mcat = 72 mg.L-1 , CFA = 2 mg.L-1 and tIRR = 65 minutes, resulting in EffDCF(%) = 90.39%. The developed photocatalyst significantly degraded the drugs and demonstrated promise for photocatalysis applications.