TY - JOUR
T1 - The effect of concentration of phenols on their batch methanogenesis
AU - Wang, Yi‐Tin ‐T
AU - Suidan, Makram T.
AU - Pfeffer, John T.
AU - Najam, Issam
PY - 1989/4/20
Y1 - 1989/4/20
N2 - The biodegradability of phenol and six other phenolic compounds (o‐, m‐, and p‐cresol, 2‐, 3‐, and 4‐ethylphenol) was examined in batch methanogenic cultures. The effect of concentration of these alkyl phenols on the anaerobic biodegradation of phenol was also evaluated. The inoculum used in this study was cultivated in a continuous flow laboratory fermenter with phenol as the primary substrate. Phenol, at initial concentrations as high to 1400 mg/L was completely degraded to methane and carbondioxide after 350 hours incubation. Complete degradation of m‐ and p‐cresol was also observed while the ethylphenols and o‐cresol were not significantly degraded. At initial concentrations exceeding 600 mg/L, phenol inhibited the phenol‐degrading microorganisms but not the methanogens. At about 600 mg/L, cresols reduced the rate of phenol degradation to 50% of that observed in a control culture containing only 200 mg/L phenol. Ethylphenols were more inhibitory than cresols. Phenol degrading microorganisms were more susceptible to inhibition by cresols and ethylphenols than were the methanogens. The inhibitory effects of the three isomers of cresol and ethylphenol did not vary with the isomer but rather with the substituted functional group.
AB - The biodegradability of phenol and six other phenolic compounds (o‐, m‐, and p‐cresol, 2‐, 3‐, and 4‐ethylphenol) was examined in batch methanogenic cultures. The effect of concentration of these alkyl phenols on the anaerobic biodegradation of phenol was also evaluated. The inoculum used in this study was cultivated in a continuous flow laboratory fermenter with phenol as the primary substrate. Phenol, at initial concentrations as high to 1400 mg/L was completely degraded to methane and carbondioxide after 350 hours incubation. Complete degradation of m‐ and p‐cresol was also observed while the ethylphenols and o‐cresol were not significantly degraded. At initial concentrations exceeding 600 mg/L, phenol inhibited the phenol‐degrading microorganisms but not the methanogens. At about 600 mg/L, cresols reduced the rate of phenol degradation to 50% of that observed in a control culture containing only 200 mg/L phenol. Ethylphenols were more inhibitory than cresols. Phenol degrading microorganisms were more susceptible to inhibition by cresols and ethylphenols than were the methanogens. The inhibitory effects of the three isomers of cresol and ethylphenol did not vary with the isomer but rather with the substituted functional group.
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U2 - 10.1002/bit.260331020
DO - 10.1002/bit.260331020
M3 - Letter
C2 - 18587872
AN - SCOPUS:0024652445
SN - 0006-3592
VL - 33
SP - 1353
EP - 1357
JO - Biotechnology and Bioengineering
JF - Biotechnology and Bioengineering
IS - 10
ER -