Avaliação de métodos de preparo de amostra para a determinação de halogênios em alumina de alta pureza

Detalhes bibliográficos
Ano de defesa: 2011
Autor(a) principal: Hoehne, Lucélia
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
BR
Química
UFSM
Programa de Pós-Graduação em Química
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://repositorio.ufsm.br/handle/1/4211
Resumo: The presence of trace elements in high purity alumina (e.g. halogens) can compromise the final product characteristics. In this work, different sample preparation methods based on alkaline fusion, halogen extraction in water with and without microwave heating, alkaline extraction, microwave-induced combustion and pyrohydrolysis for further halogens determination were evaluated. Bromine and iodine were determined by inductively coupled plasma mass spectrometry (ICP-MS). Chlorine was determined by inductively coupled plasma optical emission spectrometry, ICP-MS, ion chromatography (IC) and ion-selective electrode. Fluorine was determined by IC, ion-selective electrode and molecular absorption spectrometry with graphite furnace vaporization. No statistical difference was observed (ANOVA, 95% confidence level) between microwave induced combustion and pyrohydrolysis results for Br, Cl, F and I. These methods were considered as more suitable for further halogen determination. Relative standard deviations were lower than 18% for all analytes. For microwave induced combustion, the use of microcrystalline cellulose was necessary as a combustion auxiliary for all halogens. Pellets up to 0.5 g of sample (exceptionally for I, 0.2 g) and 0.5 g of microcrystalline cellulose were used, with 6 mL of 50 mmol L-1 (NH4)2CO3 as absorbing solution. For I the use of V2O5 (0.4 g) was also necessary. For pyrohydrolysis, all halogens were extracted with the following conditions: absorbing solution 50 mmol L-1 (NH4)2CO3, 10 min of reaction time, reactor temperature of 950 °C and 0.2 L min-1 of compressed air flow-rate.