SciELO - Scientific Electronic Library Online

 
 número55Degradation and adsorption of AZO RR239 dye in aqueous solution by nanoscale zerovalent iron particles immobilized on sawdust índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Em processo de indexaçãoCitado por Google
  • Não possue artigos similaresSimilares em SciELO
  • Em processo de indexaçãoSimilares em Google

Compartilhar


Revista Facultad de Ingeniería Universidad de Antioquia

versão impressa ISSN 0120-6230versão On-line ISSN 2422-2844

Resumo

ROJAS SARMIENTO, Hugo Alfonso; MARTINEZ ZAMBRANO, José Jobanny  e  REYES, Patricio Alberto. Kinetic study of the hydrogenation of trans-cinnamaldehyde over Ir/Nb2O5 catalysts. Rev.fac.ing.univ. Antioquia [online]. 2010, n.55, pp.9-17. ISSN 0120-6230.

The hydrogenation of trans-cinnamaldehyde was studied over Ir/Nb2O5 catalysts reduced at 473 K (LTR) and 773 K (HTR). The catalysts were characterized by N2 physisorption at 77 K, H2 chemisorption, TPR, and TPD- NH3. Kinetic study of trans-cinnamaldehyde over Ir/Nb2O5 reduced at HTR was carried out in n-heptane at hydrogen pressures in the range of 0.48 to 0.98 MPa, the reaction temperatures were 323-363 K, catalyst loadings 0.1 to 0.3 g and cinnamaldehyde concentrations 0.025 to 0.1 M. Trans-cinnamaldehyde can be selectively hydrogenated to cinnamyl alcohol although the support acidity leads to the formation of byproducts. A Langmuir-Hinshelwood model with molecular adsorption of hydrogen non competitive with organic molecules and considering the surface reaction as the rate-controlling step provided the best fit of the experimental data.

Palavras-chave : Nb2O5; hydrogenation; trans-cinnamaldehyde; SMSI effect; Langmuir-Hinshelwood.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )

 

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons