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Trichloroethene and cis ‐1,2‐dichloroethene concentration‐dependent toxicity model simulates anaerobic dechlorination at high concentrations. II: Continuous flow and attached growth reactors
Author(s) -
Sabalowsky Andrew R.,
Semprini Lewis
Publication year - 2010
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.22822
Subject(s) - chemistry , toxicity , reductive dechlorination , batch reactor , chromatography , bioreactor , continuous stirred tank reactor , electron donor , biodegradation , environmental chemistry , organic chemistry , catalysis
A model that was used to describe toxicity from high concentrations of chlorinated aliphatic hydrocarbons (CAHs) on reductively dechlorinating cultures in batch reactors (Sabalowsky and Semprini (in press)) was extended here to simulate observations in continuous flow suspended and attached growth reactors. The reductively dechlorinating anaerobic Evanite subculture (EV‐cDCE) was fed trichloroethene (TCE) and excess electron donor to accumulate cis ‐1,2‐dichloroethene (cDCE) in a continuous flow stirred tank reactor (CFSTR); and an attached growth recirculating packed column (RPC). A concentration‐dependent toxicity model used to simulate the results of batch reactors in part I (Sabalowsky and Semprini (in press) Biotechnol Bioeng) also simulated well the observations for the CFSTR and RPC growth modes. The toxicity model incorporates cDCE and TCE toxicity coefficients that directly increase the cell decay coefficient in proportion with cDCE and TCE concentrations. Simulated estimates of the cDCE and TCE toxicity coefficients indicate reductively dechlorinating cells are most sensitive to high concentrations of cDCE and TCE in batch‐fed growth, followed by CFSTR, with attached growth being least sensitive. The greater toxicity of TCE than cDCE, and ratio of the modeled toxicity coefficients, agrees with previously proposed models relating toxicity to partitioning in the cell wall ( K M/B ), proportional to octanol‐water partitioning ( K OW ) coefficients. Biotechnol. Bioeng. 2010;107: 540–549. © 2010 Wiley Periodicals, Inc.