INVESTIGADORES
BETTI carolina Paola
artículos
Título:
Nanoparticles of tungsten as low-cost monometallic catalyst for selective hydrogenation of 3-hexyne
Autor/es:
M. JULIANA MACCARRONE; CECILIA R. LEDERHOS; CAROLINA P. BETTI; NICOLÁS R. CARRARA; JUAN C. YORI; FERNANDO COLOMA-PASCUAL; DOMINGO LIPRANDI; CARLOS R. VERA; MÓNICA E. QUIROGA
Revista:
QUíMICA NOVA
Editorial:
SOC BRASILEIRA QUIMICA
Referencias:
Lugar: San Pablo; Año: 2016 vol. 39 p. 1 - 8
ISSN:
0100-4042
Resumen:
Low cost tungsten monometallic catalysts with variable amounts of metal (4.5, 7.1 and 8.5 %W) were prepared by impregnating alumina with ammonium metatungstate as an inexpensive precursor. The catalysts were characterized using ICP, XPS, XRD, TPR and hydrogen chemisorption. These techniques revealed mainly WO3-Al2O3 (W6+) species on the surface.The effects of the content of W nanoparticles and the reaction temperature on the activity and selectivity for the partial hydrogenation of 3-hexyne, a non terminal alkyne, were assessed at moderate conditions of temperature and pressure.The prepared monometallic catalysts were found to be active and stereoselective for the production of (Z)-3-hexene, showing the following order: 7.1WN/A > 8.5 WN/A ≥ 4.5 WN/A. Additionally, the performance of the synthesized xWN/A catalysts exhibited a high sensitivity to the variation of temperature. In all the cases, the maximum 3-hexyne total conversion and selectivity was achieved at 323 K.The performance of the catalysts was considered to be a consequence of two phenomena: a) the electronic effects, related to the high charge of W (+6), causing an intensive dipole moment in the hydrogen molecule (van der Waals forces) and leading to a heterolytic bond rupture; the generated H+ and H- species would approach a 3-hexyne adsorbate molecule and would provoke the heterolytic rupture of the CC bond into C- = C+; and b) steric effects related to the high concentration of WO3 on 8.5WN/A that would block the Al2O3 support. Catalyst deactivation was detected, starting at about 50 min of reaction time. Electrodeficient W6+ species would be responsible for the formation of green oil at the surface level, blocking pores and active sites of the catalyst, particularly at low reaction temperatures (293 and 303 K).The resulting best catalyst, 7.1WN/A, has both a low cost of fabrication and a high selectivity to (Z)-3-hexene (94%) at 323 K. This selectivity is comparable to that of the classical and more expensive industrial Lindlar catalyst (5 wt% Pd).The alumina supported tungsten catalysts could be low-cost potential replacements of the Lindlar industrial catalyst. They could also be used for preparing bimetallic W-Pd catalysts for selective hydrogenation of terminal and non-terminal alkynes.