Open Access
Development and demonstration of biosorbents for clean-up of uranium in water. CRADA final report
Author(s) -
B. D. Faison,
Michael Z. Hu,
John M. Norman,
Mark E. Reeves,
Lynn Williams,
W.-J. Schmidt-Kuster,
K. Darnell
Publication year - 1997
Language(s) - English
Resource type - Reports
DOI - 10.2172/676897
Subject(s) - uranium , chemistry , biosorption , langmuir adsorption model , adsorption , nuclear chemistry , environmental chemistry , biomass (ecology) , inorganic chemistry , organic chemistry , sorption , biology , materials science , metallurgy , ecology
Pseudomonas aeruginosa strain CSU, a nongenetically engineered bacterial strain known to bind dissolved hexavalent uranium, shows particular promise as the basis of an immobilized-cell process for removal of dissolved uranium from contaminated wastewaters. It was characterized with respect to its sorptive active. Living, heat-killed, permeabilized, and unreconstituted lyophilized cells were all capable of binding uranium. The uranium biosorption equilibrium could be described by the Langmuir isotherm. The rate of uranium adsorption increased following permeabilization of the outer and/or cytoplasmic membrane by organic solvents such as acetone. P. aeruginosa CSU biomass was significantly more sorptive toward uranium than certain novel, patented biosorbents derived from algal or fungal biomass sources. P. aeruginosa CSU biomass was also competitive with commercial cation-exchange resins, particularly in the presence of dissolved transition metals. Uranium binding by P. aeruginosa was clearly pH dependent. Uranium loading capacity increased with increasing pH under acidic conditions, presumably as a function of uranium speciation and due to the H{sup +} competition at some binding sites. Nevertheless, preliminary evidence suggests that this microorganism is also capable of binding anionic hexavalent uranium complexes. Ferric iron was a strong inhibitor of uranium binding to P. aeruginosa CSU biomass, and the presence of uranium also decreased the Fe{sup 3+} loading when the biomass was not saturated with Fe{sup 3+}, suggesting that Fe{sup 3+} and uranium may share the same binding sites on biomass