EM - Escola de Minas

URI permanente desta comunidadehttp://www.hml.repositorio.ufop.br/handle/123456789/6

Notícias

A Escola de Minas de Ouro Preto foi fundada pelo cientista Claude Henri Gorceix e inaugurada em 12 de outubro de 1876.

Navegar

Resultados da Pesquisa

Agora exibindo 1 - 5 de 5
  • Item
    Capture of CO2 by vermiculite impregnated with CaO.
    (2022) Pereira, Matheus Henrique Simplício; Santos, Cláudio Gouvêa dos; Lima, Geraldo Magela de; Bruziquesi, Carlos Giovani Oliveira; Oliveira, Victor de Alvarenga
    Vermiculite samples were impregnated with different amounts of calcium oxide by the con- ventional thermal heating technique and subject to CO2 capture experiments in thermal analysis equipment. The amount of CO2 captured by calcium oxide increased from 13 g of CO2 per mol of CaO to 16.8 g of CO2 per mol of CaO when the experiments were carried out with pure calcium oxide and vermiculite impregnated with CaO (1:1), respectively. Integral isoconversional methods of Kissinger-Akahira-Sunose (KAS) and Osawa-Flynn-Wall (OFW) were used for the kinetic study of the process and good correlation coefficients were achieved. The apparent activation energy values showed that for low conversions (a < 0.3) the controlling step of the process is a mixed step where the chemical reaction and the dif- fusion of the reagents into the vermiculite have rates of the same order of magnitude (20 kJ < Ea < 40 kJ). For higher conversions values (a > 0.3) the apparent activation energy values suggest that the slow step is a chemical step (Ea> 40 kJ).
  • Item
    Effect of iron in zinc silicate concentrate on leaching with sulphuric acid.
    (2009) Souza, Adelson Dias de; Pina, Pablo dos Santos; Santos, Fabiano Mariel Fernandes dos; Silva, Carlos Antônio da; Leão, Versiane Albis
    It is shown that the iron content in zinc silicate concentrates with either high (8–11%) or low (3%) iron does not significantly affect the kinetics or overall recovery of zinc extraction in sulphuric acid. Most of the iron was present as hematite and franklinite with little iron contained in willemite. A small reduction in zinc recovery from 98.5% to 97.5% was observed for silicate ores containing 12% iron. The activation energy determined from high-iron concentrate leaching, 78±12 kJ/mol, is statistically similar to that from low-iron concentrate, 67±10 kJ/mol, suggesting the same rate-controlling step. The leaching of high high-iron concentrates enables a higher mass recovery during flotation. A flowsheet is proposed comprising a magnetic separation step to produce a magnetic and a non-magnetic product so that iron dissolution from the magnetic concentrate acts as a source of soluble iron for impurities removal.
  • Item
    Adsorption of chromium (VI) ion from aqueous solution by succinylated mercerized cellulose functionalized with quaternary ammonium groups.
    (2009) Gurgel, Leandro Vinícius Alves; Melo, Júlio César Perin de; Lena, Jorge Carvalho de; Gil, Laurent Frédéric
    Succinylated mercerized cellulose (cell 1) was used to synthesize an anion exchange resin. Cell 1, containing carboxylic acid groups was reacted with triethylenetetramine to introduce amine functionality to this material to obtain cell 2. Cell 2 was reacted with methyl-iodide to quaternize the amine groups from this material to obtain cell 3. Cells 2 and 3 were characterized by mass percent gain, degree of amination and quaternization, FTIR and CHN. Cells 2 and 3 showed degrees of amination and quaternization of 2.8 and 0.9 mmol/g and nitrogen content of 6.07% and 2.13%, respectively. Cell 3 was used for Cr (VI) adsorption studies. Adsorption equilibrium time and optimum pH for Cr (VI) adsorption were found to be 300 min and 3.1, respectively. The Langmuir isotherm was used to model adsorption equilibrium data. The adsorption capacity of cell 3 was found to be 0.829 mmol/g. Kinetic studies showed that the rate of adsorption of Cr (VI) on cell 3 obeyed a pseudo-second-order kinetic model.
  • Item
    A kinetic study of the sulphuric acid leaching of a zinc silicate calcine.
    (2007) Souza, Adelson Dias de; Pina, Pablo dos Santos; Lima, Ermani Vinicius de Oliveira; Silva, Carlos Antônio da; Leão, Versiane Albis
    Recent developments of acid leaching and solvent extraction of zinc silicate ores have produced renewed commercial interest. However, the leaching kinetics of these concentrates has received little attention. This work, therefore, addresses the leaching of a zinc silicate concentrate in sulphuric acid. The effects of particle size (0.038–0.075mm), temperature (30–50°C) and initial acid concentration (0.2–1.0mol/L) were studied. The results show that decreasing the particle size while increasing the temperature and acid concentration increase the leaching rate. As leaching occurs, there is a progressive dissolution of willemite whil e the quartz and iron-containing phases remain inert. Among the kinetic models of the porous solids tested, the grain model with porous diffusion control successfully described the zinc leaching kinetics. The model enabled the determination of an activation energy of 51.9 ± 2.8kJ/mol and a reaction order of 0.64 ± 0.12 with respect to sulphuric acid, which are likely to be a consequence of the parallel nature of diffusion and chemical reaction in porous solids.
  • Item
    The leaching kinetics of a zinc sulphide concentrate in acid ferric sulphate.
    (2007) Souza, Adelson Dias de; Pina, Pablo dos Santos; Leão, Versiane Albis; Silva, Carlos Antônio da; Siqueira, Priscila de Freitas
    This work examines the dissolution kinetics of an iron–rich zinc sulphide concentrate in acid ferric sulphate medium. The effects of temperature, ferric ion and sulphuric acid concentrations, agitation speed and particle size on the leaching kinetics were investigated. The leaching process could be separated into two stages. Initially, the dissolution kinetics was controlled by the chemical reaction at the surface of the zinc sulphide particles followed by a second step where the reaction was controlled by diffusion of the reagents or products through the elemental sulphur (ash) layer. The activation energy of the chemical controlled step was 27.5 kJ/mol and the value determined for the diffusion controlled step was 19.6 kJ/mol. The reaction order with respect to ferric ion and sulphuric acid concentrations were approximately 0.50 and 1.00, respectively. Analysis of the unreacted and reacted sulphide particles by SEM-EDS showed a progressive increase of the thickness of the elemental sulphur layer on the solid surface. The development of this sulphur layer is further evidence of the change on the rate-controlling step as the reaction progress.