Hidrogenação de ácido levulínico a gama-valerolactona empregando fosfetos de metais de transição suportados em sílica
Ano de defesa: | 2016 |
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Autor(a) principal: | |
Orientador(a): | |
Banca de defesa: | |
Tipo de documento: | Dissertação |
Tipo de acesso: | Acesso aberto |
Idioma: | por |
Instituição de defesa: |
Universidade Federal do Rio de Janeiro
Brasil Instituto Alberto Luiz Coimbra de Pós-Graduação e Pesquisa de Engenharia Programa de Pós-Graduação em Engenharia Química UFRJ |
Programa de Pós-Graduação: |
Não Informado pela instituição
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Departamento: |
Não Informado pela instituição
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País: |
Não Informado pela instituição
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Palavras-chave em Português: | |
Link de acesso: | http://hdl.handle.net/11422/7913 |
Resumo: | The following silica supported phosphides with loading of 30 wt% were prepared, characterized and evaluated for levulinic acid hydrogenation to γ- valerolactone: Ni2P, CoP, MoP, WP and Fe2P. The catalysts were prepared in two steps: phosphate synthesis by incipient wetness followed by calcination, and phosphide synthesis by in situ temperature programmed reduction. The samples were characterized by N2 physisorption at -196 ˚C, X-Ray diffraction, inductively coupled plasma optical emission spectrometry, CO chemisorption and temperature programed CO desorption. Temperature programed surface reaction experiments were also performed with 30 wt% Ni2P/SiO2. The catalytic evaluation were performed in a three phase trickle bed reactor, using H2 as hydrogen source and water as solvent, at 30 bar, 125 ˚C and weight hourly space velocity of 15 h -1 . In such conditions, theoretical calculations showed the absence of mass-transfer limitations. Among the evaluated phosphides, the best performance was obtained by 30 wt% Ni2P/SiO2 (conversion of 60%), based on the same weight of catalyst precursor loaded in the reactor, exhibiting a turnover frequency higher than the most effective catalyst for this reaction, 5% (m/m) Ru/C, to date. However, the supported phosphides suffered deactivation due to leaching of the active phase caused by water and increased by the presence of levulinic acid. |