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苯系物和汽油在各种水生沉积物中的厌氧生物降解

Anaerobic biodegradation of BTEX and gasoline in various aquatic sediments.

作者信息

Phelps C D, Young L Y

机构信息

Rutgers, State University of New Jersey, New Brunswick, USA.

出版信息

Biodegradation. 1999 Feb;10(1):15-25. doi: 10.1023/a:1008303729431.

Abstract

We examined the extent of biodegradation of benzene, toluene, ethylbenzene and the three isomers of xylene (BTEX) as a mixture and from gasoline in four different sediments: the New York/New Jersey Harbor estuary (polluted); Tuckerton, N.J. (pristine); Onondaga Lake, N.Y. (polluted) and Blue Mtn. Lake, N.Y. (pristine). Enrichment cultures were established with each sediment using denitrifying, sulfidogenic, methanogenic and iron reducing media, as well as site water. BTEX loss, as measured by GC-FID, was extensive in the sediments which had a long history of pollution, with all compounds being utilized within 21-91 days in the most active cultures, and was very slight or non-existent in the pristine sediments. Also, the pattern of loss was different under the various reducing conditions within each sediment and between sediments. For example benzene loss was only observed in sulfidogenic cultures from the NY/NJ Harbor sediments while toluene was degraded under all redox conditions. The loss of BTEX was correlated to the reduction of the various electron acceptors. In cultures amended with gasoline the degradation was much slower and incomplete. These results show that the fate of the different BTEX components in anoxic sediments is dependent on the prevailing redox conditions as well as on the characteristics and pollution history of the sediment.

摘要

我们研究了苯、甲苯、乙苯以及二甲苯的三种异构体(BTEX)作为混合物以及来自汽油的情况下,在四种不同沉积物中的生物降解程度:纽约/新泽西港河口(受污染);新泽西州塔克顿(原始);纽约州奥农达加湖(受污染)和纽约州蓝山湖(原始)。使用反硝化、产硫化物、产甲烷和铁还原培养基以及现场水,用每种沉积物建立富集培养物。通过气相色谱 - 火焰离子化检测器(GC - FID)测量,BTEX的损失在有长期污染历史的沉积物中很广泛,在最活跃的培养物中所有化合物在21 - 91天内被利用,而在原始沉积物中非常轻微或不存在。此外,每种沉积物内以及沉积物之间在各种还原条件下损失模式不同。例如,仅在纽约/新泽西港沉积物的产硫化物培养物中观察到苯的损失,而甲苯在所有氧化还原条件下都被降解。BTEX的损失与各种电子受体的还原相关。在用汽油改良的培养物中,降解要慢得多且不完全。这些结果表明,缺氧沉积物中不同BTEX组分的归宿取决于主要的氧化还原条件以及沉积物的特性和污染历史。

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