Surface Complexation of Neptunium(V) onto Whole Cells and Cell Components of Shewanella alga: Modeling and Experimental Study
| Autor: | Bruce E. Rittmann, Warinthorn Songkasiri, Randhir P. Deo, Donald T. Reed |
|---|---|
| Rok vydání: | 2010 |
| Předmět: |
Shewanella
Polymers Surface Properties Ultraviolet Rays Stereochemistry Inorganic chemistry Ligands Neptunium Deprotonation Cell Wall Environmental Chemistry Amines chemistry.chemical_classification Aqueous solution biology Chemistry Sorption General Chemistry Hydrogen-Ion Concentration Models Theoretical biology.organism_classification Amino acid Stability constants of complexes Amine gas treating Titration Adsorption Oxidation-Reduction Environmental Monitoring |
| Zdroj: | Environmental Science & Technology. 44:4930-4935 |
| ISSN: | 1520-5851 0013-936X |
| DOI: | 10.1021/es9035336 |
| Popis: | We systematically quantified surface complexation of Np(V) onto whole cells, cell wall, and extracellular polymeric substances (EPS) of Shewanella alga strain BrY. We first performed acid and base titrations and used the mathematical model FITEQL to estimate the concentrations and deprotonation constants of specific surface functional groups. Deprotonation constants most likely corresponded to a carboxyl group not associated with amino acids (pK(a) approximately 5), a phosphoryl site (pK(a) approximately 7.2), and an amine site (pK(a)10). We then carried out batch sorption experiments with Np(V) and each of the S. alga components as a function of pH. Since significant Np(V) sorption was observed on S. alga whole cells and its components in the pH range 2-5, we assumed the existence of a fourth site: a low-pK(a) carboxyl site (pK(a) approximately 2.4) that is associated with amino acids. We used the SPECIATE submodel of the biogeochemical model CCBATCH to compute the stability constants for Np(V) complexation to each surface functional group. The stability constants were similar for each functional group on S. alga bacterial whole cells, cell walls, and EPS, and they explain the complicated sorption patterns when they are combined with the aqueous-phase speciation of Np(V). For pH8, the aquo NpO(2)(+) species was the dominant form of Np(V), and its log K values for the low-pK(a) carboxyl, mid-pK(a) carboxyl, and phosphoryl groups were 1.8, 1.8, and 2.5-3.1, respectively. For pH greater than 8, the key surface ligand was amineXNH(3)(+), which complexed with NpO(2)(CO(3))(3)(5-). The log K for NpO(2)(CO(3))(3)(5-) complexed onto the amine groups was 3.1-3.9. All of the log K values are similar to those of Np(V) complexes with aqueous carboxyl and N-containing carboxyl ligands. These results help quantify the role of surface complexation in defining actinide-microbiological interactions in the subsurface. |
| Databáze: | OpenAIRE |
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