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Bioaugmentation of an anaerobic biotrickling filter for enhanced conversion of trichloroethene to ethene

机译:厌氧生物滴滤池的生物强化,可提高三氯乙烯向乙烯的转化率

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During biological reduction of trichloroethene (TCE), incomplete reduction to partially dechlorinated intermediates cis-1,2-dichloroethene (cis-DCE) and vinyl chloride (VC) can occur due to kinetic and inhibitory limitations. In this study, an anaerobic biotrickling filter was inoculated initially with a mixed culture containing Dehalococcoides spp. that contained the TceA and VcrA reductive dehalogenases. After significant accumulation of cis-DCE and VC was observed in the bioreactor effluent, it was hypothesized that bioaugmentation with Dehalococcoides strain BAV1, which contains the BvcA dehalogenase responsible for the metabolic dechlorination of cis-DCE and VC, would improve the conversion of TCE to ethene. It was found that at TCE loadings of 8-9 g m_(bed)~(-3) h~(-1), bioaugmentation with strain BAV1 resulted in 45% conversion of TCE to ethene, as opposed to less than 10% prior to bioaugmentation. Strain BAV1 was found to grow to the same density (10~6-10~7 cells per g of packing material) as Dehalococcoides strains containing the TceA and VcrA dehalogenases. Strain BAV1 was also confirmed to be active, as determined by RT-qPCR of the BvcA mRNA. This study shows that it is possible to enhance the performance of continuously fed dechlorinating bioreactors by using a consortium that contains all three known reductive dehalogenases in the TCE dechlorination pathway. This is also the first study where a gas-phase biotrickling filter has been bioaugmented with a single strain to result in improved performance.
机译:在生物还原三氯乙烯(TCE)的过程中,由于动力学和抑制性限制,可能会发生不完全还原为部分脱氯的中间体顺式1,2,2-二氯乙烯(cis-DCE)和氯乙烯(VC)的情况。在这项研究中,首先用含有Dehalococcoides spp的混合培养物接种厌氧生物滴滤池。含有TceA和VcrA还原性脱卤酶。在生物反应器流出物中观察到大量的顺式DCE和VC积累后,假设用Dehaloccocoides菌株BAV1进行生物强化,该菌株包含负责顺式DCE和VC代谢脱氯的BvcA脱卤素酶。乙烯。发现在8-9 g m_(bed)〜(-3)h〜(-1)的TCE负载下,菌株BAV1的生物强化导致TCE转化为乙烯的转化率为45%,而之前的转化率不到10%进行生物强化。发现BAV1菌株的生长密度与含有TceA和VcrA脱卤酶的Dehalococcoides菌株相同(每g包装材料10〜6-10〜7个细胞)。如BvcA mRNA的RT-qPCR所确定,菌株BAV1也被证实具有活性。这项研究表明,通过在TCE脱氯途径中使用包含所有三种已知的还原性脱卤素酶的联合体,可以提高连续进料的脱氯生物反应器的性能。这也是首次对气相生物滴流过滤器进行单一菌株生物强化以提高性能的研究。

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