Cja. Mota et R. Rawet, MECHANISM OF AROMATIC HYDROCARBON FORMATION IN FCC NAPHTHA, Industrial & engineering chemistry research, 34(12), 1995, pp. 4326-4332
A microactivity test study of the FCC naphtha composition at increasin
g conversions was carried out. At low conversions (ca. 10-20%), the na
phtha is rich in olefinic and aromatic hydrocarbons. As the conversion
increases, the composition changes dramatically. The olefins initiall
y increase and then decrease sharply. The paraffins increase continual
ly, and the aromatics initially decrease and then increase slightly. T
he naphthenics remain constant in the conversion range studied. These
results indicate that, at low conversions, the aromatics in the gasoli
ne are mainly formed by dealkylation of heavy aromatic molecules prese
nt in the feed. At higher conversions, however, the aromatics in the n
aphtha are mainly formed by cyclization followed by hydrogen transfer
of the olefins formed during cracking. This reaction also increases th
e relative concentration of paraffinic hydrocarbons. The distribution
of C9 aromatics showed that, as the conversion increases, there occurs
an isomerization of the alkyl chain, to increase the branching of the
ring.