226 Ra, 238 U and Cd adsorption kinetics and binding capacity of two cyanobacterial strains isolated from highly radioactive springs and optimal conditions for maximal removal effects in contaminated water
Biomass-based decontamination methods are among the most interesting water treatment techniques. In this study, 2 cyanobacterial strains, Nostoc punctiforme A.S/S4 and Chroococcidiopsis thermalis S.M/S9, isolated from hot springs containing high concentrations of radium ( Ra), were studied to be ass...
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Published in | International journal of phytoremediation Vol. 20; no. 4; pp. 369 - 377 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
21.03.2018
|
Subjects | |
Online Access | Get full text |
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Summary: | Biomass-based decontamination methods are among the most interesting water treatment techniques. In this study, 2 cyanobacterial strains, Nostoc punctiforme A.S/S4 and Chroococcidiopsis thermalis S.M/S9, isolated from hot springs containing high concentrations of radium (
Ra), were studied to be associated with removal of radionuclides (
U and
Ra) and heavy metal cadmium (Cd) from aqueous solutions. The adsorption equilibrium data was described by Langmuir and Freundlich isotherm models. Kinetic studies indicated that the sorption of 3 metals followed pseudo-second-order kinetics. Effects of biomass concentration, pH, contact time, and initial metal concentration on adsorption were also investigated. Fourier-transform infrared spectroscopy revealed active binding sites on the cyanobacterial biomass. The obtained maximum biosorption capacities were 630 mg g
and 37 kBq g
for
U and
Ra for N. punctiforme and 730 mg g
and 55 kBq g
for C. thermalis. These 2 strains showed maximum binding capacity 160 and 225 mg g
, respectively for Cd adsorption. These results suggest that radioactivity resistant cyanobacteria could be employed as an efficient adsorbent for decontamination of multi-component, radioactive and industrial wastewater. |
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ISSN: | 1522-6514 1549-7879 |
DOI: | 10.1080/15226514.2017.1393392 |