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dc.contributor.authorMatos, Vanderson Eney de-
dc.contributor.authorPeres, Antônio Eduardo Clark-
dc.contributor.authorPereira, Carlos Alberto-
dc.contributor.authorNogueira, Stephânia da Consolação Silva-
dc.date.accessioned2020-05-27T14:13:32Z-
dc.date.available2020-05-27T14:13:32Z-
dc.date.issued2019-
dc.identifier.citationMATOS, V. E. de. et al. Analysis of quartz floatability using design of experiments. REM - International Engineering Journal, Ouro Preto, v. 27, n. 3, p. 501-506, jul./set. 2019. Disponível em: <http://www.scielo.br/scielo.php?script=sci_abstract&pid=S2448-167X2019000400501&lng=en&nrm=iso>. Acesso em: 10 mar. 2020.pt_BR
dc.identifier.issn1807-0353-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/12265-
dc.description.abstractQuartz floatability in cationic reverse flotation depends on the suitable choice of surfactant type and the conditions under which they are applied. The design of experiments (DOE) allows the evaluation of process variables, in a structured and independent way, with statistical validation and a limited number of tests. Tests of microflotation of quartz, in the size range -150 +75 µm, using factorial design of experiments, showed that etherdiamine leads to higher level of quartz floatability than ethermonoamine, favored by increase in collector concentration, at the high level of pH tested (11.0). Floatability values above 90% were achieved with the use of 3 mg/L of ether diamine for both pH levels, while with ether monoamine the target was reached only at pH 11.pt_BR
dc.language.isopt_BRpt_BR
dc.rightsabertopt_BR
dc.subjectEthermonoaminept_BR
dc.subjectEtherdiaminept_BR
dc.subjectMicroflotationpt_BR
dc.titleAnalysis of quartz floatability using design of experiments.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.rights.licenseA REM - International Engineering Journal - autoriza o depósito de cópia de artigos dos professores e alunos da UFOP no Repositório Institucional da UFOP. Licença concedida mediante preenchimento de formulário online em 12 set. 2013.pt_BR
dc.identifier.doihttp://dx.doi.org/10.1590/0370-44672018720080pt_BR
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