SciELO - Scientific Electronic Library Online

 
vol.23 issue7Mechanistic implications of zinc(II) ions on the degradation of phenol by the fenton reactionChemometric tools in chemical fractionation data of soil samples from five antarctic research stations author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Journal of the Brazilian Chemical Society

Print version ISSN 0103-5053

Abstract

PUJRO, Richard A. et al. Yield of aromatics from naphthenics upon catalytic cracking. J. Braz. Chem. Soc. [online]. 2012, vol.23, n.7, pp. 1378-1387. ISSN 0103-5053.  http://dx.doi.org/10.1590/S0103-50532012000700023.

Cis- and trans-decalin were reacted over cracking catalysts to study the formation of aromatics in a particular fraction of the liquid products obtained in the fluid catalytic cracking process (FCC). A batch, fluidized bed CREC riser simulator reactor was used at 673 and 723 K and contact times varied from 3 to 15 s. Cis-decalin was much more reactive. Despite differences induced and measured in their accessibility indices, the catalysts led to similar activity profiles, suggesting that diffusion restrictions do not prevail. Products were C1-C12 hydrocarbons while coke was very low. Isomerization, cracking, hydrogen transfer, ring opening, ring contraction and alkylation reactions occurred and products from the various reactions were observed at very short reaction times. Bicyclic C10 naphthenics and alkyl-substituted C7-C11 aromatics or naphtheno-aromatics were the most important products. A reaction mechanism with three initial routes (isomerization, ring opening and direct hydrogen transfer reactions) was proposed.

Keywords : aromatics; Y zeolite; decalin; cracking; hydrogen transfer.

        · abstract in Portuguese     · text in English     · pdf in English