skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Adsorption of organic compounds by microbial biomass

Miscellaneous ·
OSTI ID:5605908

The adsorption of hazardous organic compounds such as phenol, 2-chlorophenol, 2-nitrophenol, chlorobenzene, and ethylbenzene onto two types of inactive microbial biomass (activated sludge and nitrifying bacteria) was studied. The adsorption isotherms could be expressed by the Freundlich adsorption isotherm and were found to be nearly linear over the range of concentrations (50-200 mg/l) studied. Desorption studies showed that the adsorption process was partially reversible. Heat of sorption was estimated and indicate that the biosorption process involves a physical rather than a chemical mechanism. The adsorptive capacity of biomass is about two to three orders of magnitude less than activated carbon. In bisolute systems, the uptake of each solute is reduced in the presence of a second solute, but the combined adsorptive capacity was greater than that for either of the individual substances from its pure solution. The compound with higher octanol/water partition coefficient was observed to be more favorably adsorbed. In the case of activated carbon, the more hydrophobic compound was observed to be more favorably adsorbed. The uptake of each solute is reduced, when the initial concentration of other solute is increased. In multi-solute systems, the equilibrium capacity for each solute is reduced significantly in the presence of other solutes and the effect of competition become more pronounced with the increase in number of solutes in solution. The overall adsorption capacity of biomass was barely affected by the presence of more solutes in solution. Live and inactive biomass do not exhibit the same level of biosorptive uptake, and the differences appear to depend on the specific organic compound.

Research Organization:
New Jersey Inst. of Tech., Newark, NJ (United States)
OSTI ID:
5605908
Resource Relation:
Other Information: Thesis (Ph. D.)
Country of Publication:
United States
Language:
English