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Biodegradation kinetics and interactions of styrene and ethylbenzene as single and dual substrates for a mixed bacterial culture

Hazrati, H ; Sharif University of Technology | 2015

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  1. Type of Document: Article
  2. DOI: 10.1186/s40201-015-0230-y
  3. Publisher: BioMed Central Ltd , 2015
  4. Abstract:
  5. This study examined biodegradation kinetics of styrene and ethylbenzene as representatives of alkenylbenzenes and mono-alkylbenzenes, respectively. The compounds were studied independently and as binary mixtures using a series of aerobic batch degradation experiments introduced by acclimatized mix culture. Initial concentration of styrene and ethylbenzene in the liquid phase vacillated from 0 to 220 mg/l. The Andrew model was applied for the biodegradation of individual substrates and the estimated constants of the equation for styrene and ethylbenzene were μmax = 0.1581, 0.2090 (1/h), KS =25.91, 37.77 (mg/L), KI =13.15, 62.62 (mg/L), respectively. The accomplished parameters from single substrate degradation tests were used to predict possible interaction factors achieved from dual substrate experiments. The Sum Kinetics with Interaction Parameters (SKIP) model and the purely competitive enzyme kinetics model were employed to evaluate any interactions. The SKIP model was found to accurately describe these interactions. Moreover, it was revealed that ethylbenzene plays an influential role on styrene consumption (e.g. IE,S = 1.64) compared to styrene which has insignificant inhibitory effect on ethylbenzene usage (e.g. IS,E =0.4) . The active site differences for styrene and ethylbenzene biodegradation and the pathway variations for biodegradation are among the major potential reasons for failure of the estimation that occurred in purely competitive kinetics model. This study is the first to calculate the interactions between styrene and ethylbenzene
  6. Keywords:
  7. Andrews model ; Ethylbenzene ; Mixed culture ; SKIP model ; Styrene
  8. Source: Journal of Environmental Health Science and Engineering ; 2015 ; 2052336X (ISSN)
  9. URL: http://jehse.biomedcentral.com/articles/10.1186/s40201-015-0230-y