L. Setti et al., DIFFUSION AS A RATE CONTROLLING STEP IN HEAVY-OIL BIODESULFURIZATION PROCESSES, Fuel processing technology, 40(2-3), 1994, pp. 311-317
Microbial degradation of hydrocarbons depends on various chemical and
physical factors (viz, temperature, electron accepters, nutrients, pH,
substrate characteristics) and on the presence of degrading microorga
nisms. Even if all these factors are optimized, oil biodegradation can
still be retarded by diminished availability of the compound. Setti e
t al. (1992) have shown that n-alkanes affect the biodegradation of ar
omatic sulfur compounds by an aerobic Pseudomonas sp. This communicati
on illustrates further investigations into the diffusion effect that c
ontrols the biodegradation of aromatic sulfur compounds. Polycyclic ar
omatic hydrocarbons (PAHs) can be converted in the dissolved state onl
y. This implies that mass-transfer from the solid phase to the aqueous
phase might be rate-limiting. Dibenzothiophene (DBT) biodegradation i
s a good example of this model. The presence of a fatty acid (hexadeca
noic acid, aC16) during the fermentation affects DBT degradation. We p
ropose a model in which aC16 surrounds the DBT molecule forming a mice
lle which favors a co-metabolic process between the fatty acid and the
aromatic sulfur compound. Similar behavior is seen when DBT is dissol
ved in n-dodecane(C12) and n-hexadecane (C16). There are two important
parameters that affect DBT degradation in this system: the surface ar
ea of the substrate and the DBT concentration in C12. DBT degradation
is limited by the diffusion of the sulfur compound from the organic ph
ase to the adsorbed microorganism on the hydrocarbon. Diffusion increa
ses with the DBT concentration, and the DBT degradation rate is signif
icantly higher than that reported for DBT alone. In this case, a carri
er effect of the n-alkane in the DBT degradation is shown. A barrier e
ffect is suggested when the DBT concentration is below the limit for w
hich the degradation rate is lowest. Our investigations show that the
presence of a co-substrate, such as fatty acids or n-alkanes, affects
the bioavailability of the aromatic sulfur compound in aerobic conditi
ons.