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EFFECTS OF REDOX CONDITIONS AND COSUBSTRATES ON BIODEGRADATION OF PAH-CONTAMINATED MARINE SEDIMENT

机译:氧化还原条件和补充剂对PAH受污染海洋沉积物生物降解的影响

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Polycyclic aromatic hydrocarbons (PAHs) are a cause for concern due to their hazardous properties and recalcitrance. To facilitate cost-effective in-situ bioremediation of PAHs in the future, this study examined the potential of PAHs biodegradation in contaminated marine sediment by indigenous microbial consortia under three redox conditions: aerobic, sulfate reducing and denitrifying conditions using bench-scale reactor systems. Enhanced biodegradation under aerobic, denitrifying and sulfate reducing conditions promoted by the addition of the cosubstrates was also examined. Acetate and ethanol were used to stimulated anaerobic biodegradation while ethanol and salicylic acid were the cosubstrates in the aerobic studies. The effect on PAH biodegradation of facilitated solubilization by a nonionic surfactant, Triton X-100, was also evaluated in the aerobic experiments. The sediment used in this study was the PAH contaminated East River sediment collected near Rikers Island, NY. A critical factor in aerobic PAHs biodegradation in marine sediment is the availability of a sufficient supply of oxygen to overcome the initial oxygen depletion due to the high content of sulfide in the sediment. With sufficient oxygen, significant degradation of all 2-, 3-, 4- and 5- ring PAHs was achieved. Although lower ring compounds degraded faster than the higher ring PAHs, it was observed that those compounds present at higher initial concentration in the sediment exhibited higher degrees of degradation than those present at lower concentrations. This observation may be attributed to the bioavailability of these compounds in the aqueous phase. Nitrogen and phosphorus were present in sufficient quantities in this sediment to support biodegradation and additional supply of these nutrients did not accelerate biodegradation. In the presence of sulfate, PAHs degraded simultaneously with sulfate reduction, though the extent and rate of degradation was much lower than that observed under aerobic conditions. The addition of the cosubstrates ethanol and acetate under sulfate reducing conditions led to an enhancement of the rate of PAH biodegradation. Under denitrifying condition, no appreciable PAHs degradation was observed during an incubation period of 4 months, which may be attributed to an insufficient population of PAH degrading denitrifying organisms in the sediment. The immediate decrease in nitrate concentration, the simultaneous increase in sulfate concentration, and the production of nitrogen gas suggested the predominance of autotrophic denitrifying microorganisms in the sediment.
机译:多环芳香烃(PAH)是引起人们的关注,因为它们危险特性和不顺应。为了便于在以后多环芳烃成本效益的原位生物修复,本研究检查多环芳烃生物降解的电位在污染海洋沉积物土著微生物聚生体3的氧化还原条件下进行:需氧,硫酸盐还原和反硝化使用实验室规模的反应器系统的条件。通过添加共底物的促进有氧,反硝化和硫酸盐还原条件下的生物降解增强也进行了研究。乙酸盐和乙醇被用来刺激厌氧生物降解而乙醇和水杨酸是在好氧研究共底物。由非离子表面活性上易化增溶的PAH的生物降解作用,曲拉通X-100,也评价在好氧实验。在这项研究中所用的沉淀物污染东江沉积物收集附近的赖克斯岛,NY的PAH。在海洋沉积物中的有氧生物降解多环芳烃的一个关键因素是氧气克服最初氧气耗尽的充足供应的可用性由于硫化物在沉积物的含量高。具有足够的氧气,所有2-显著降解,3-,4-和5-环多环芳烃达到了。虽然较低的环化合物降解比高环多环芳烃更快,可以观察到的那些化合物呈现在沉积物较高的初始浓度在较低浓度下表现出较高的度比本降解的。这一观察结果可能归因于在水相中这些化合物的生物利用度。氮,磷存在于足够数量的这种沉积物支持生物降解和这些营养素的额外供应没有加速降解。在硫酸的存在下,与多环芳烃硫酸盐还原同时降解,虽然退化的程度和速率比需氧条件下观察到的要低得多。在加入下硫酸盐还原导致PAH生物降解的速率的增强条件共底物乙醇和乙酸盐的。下反硝化条件下,在4个月的潜伏期,这可以归因于在沉积物PAH降解反硝化生物的人口不足,观察到没有明显的多环芳烃降解。立即降低硝酸盐浓度,在硫酸盐浓度的同时增加,并且生产氮气的建议在沉积物自养脱氮微生物的优势。

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