The release of toxic metal species is of concern due to their detrimental effects on the environment and human health. Industrial effluents are a major source of mobilised metal species. Suitable technologies are needed to sequester toxic metal species at the point of source. Biosorption, which is based on the passive adsorption of contaminants onto biological materials, promises to offer an effective alternative or complementary step to existing treatment methods. However, to date there has been no widespread commercialisation of the technique. This is partly due to an insufficient understanding of the complex underlying mechanisms which makes it difficult to select suitable biomass for specific remediation problems and to predict process performance.
This study characterised two gram-positive, thermophilic bacteria, Anoxybacillus flavithermus (BF) and Geobacillus stearothermophilus (BS), harvested at two different growth times, with regard to their acid-base and Cd�⁺ adsorption behaviour. The aim was to investigate the metal cation adsorption properties of thermophilic bacteria which has not been studied previously, and to gain a better understanding of the interactions responsible for bacterial metal cation adsorption. Experimental techniques employed in this study included microscopy to establish cell and cell wall morphology, batch acid-base and Cd�⁺ adsorption experiments to quantify proton active surface functional groups and Cd�⁺ adsorption, electrophoretic mobility measurements to assess the overall surface charge of the bacteria and in situ attenuated total reflection infrared (ATR-IR) spectroscopy to reveal the chemical identities of functional groups. Chemical equilibrium models based on batch acid-base titration and electrophoretic mobility data were developed to quantitatively describe proton active surface functional groups. These groups can also interact with metal cations.
It was found that growth time was an important factor in all experiments with the differences between growth times often being more pronounced than the differences between the two bacterial strains. Microscopy revealed a gram-positive cell wall structure with different widths and staining behaviour for exponential phase cells of BF and BS. Stationary / death phase cells showed disintegrating cell walls. Acid-base titrations indicated that all cells possessed buffering capacity over the whole investigated pH range (pH 2 - 10). From electrophoretic mobility measurements, isoelectric points of ~ 3.2 for BF and < 1.8 and ~ 4.2 for exponential and stationary / death phase cells of BS respectively were estimated. Chemical equilibrium models including a Donnan electrostatic model were derived which described both the batch acid-base titration data and the electrophoretic mobility data reasonably well, although a comparison with IR data suggested room for further improvement. In situ ATR-IR spectroscopy of hydrated bacterial cells at various pH values revealed amide and carboxyl groups and a contribution from phosphate / polysaccharide moieties. Group specific interactions with Cd�⁺ were not detected, however, a partially reversible absorbance increase of all peaks suggested conformational changes in the presence of Cd�⁺. BF and BS adsorbed ~ 70 [mu]mol Cd�⁺ (g dry bacterial)⁻� at pH 5 in 0.01 M NaNO₃. Release of major cations occurred concomitantly with Cd�⁺ adsorption.
The buffering and Cd�⁺-binding capacities of BF and BS were found to be comparable to those of mesophilic bacteria and ion exchange was identified as an important adsorption mechanism.
| Identifer | oai:union.ndltd.org:ADTP/217796 |
| Date | January 2007 |
| Creators | Heinrich, Hannah Tabea Monika, n/a |
| Publisher | University of Otago. Department of Chemistry |
| Source Sets | Australiasian Digital Theses Program |
| Language | English |
| Detected Language | English |
| Rights | http://policy01.otago.ac.nz/policies/FMPro?-db=policies.fm&-format=viewpolicy.html&-lay=viewpolicy&-sortfield=Title&Type=Academic&-recid=33025&-find), Copyright Hannah Tabea Monika Heinrich |
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