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An integrated bioremediation process for petroleum hydrocarbons removal and odor mitigation from contaminated marine sediment

机译:用于从污染的海洋沉积物中去除石油烃和减少异味的综合生物修复工艺

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This study developed a novel integrated bioremediation process for the removal of petroleum hydrocarbons and the mitigation of odor induced by reduced sulfur from contaminated marine sediment. The bioremediation process consisted of two phases. In Phase I, acetate was dosed into the sediment as co-substrate to facilitate the sulfate reduction process. Meanwhile, akaganeite (beta-FeOOH) was dosed in the surface layer of the sediment to prevent S2- release into the overlying seawater. In Phase II, NO3- was injected into the sediment as an electron acceptor to facilitate the denitrification process. After 20 weeks of treatment, the sequential integration of the sulfate reduction and denitrification processes led to effective biodegradation of total petroleum hydrocarbons (TPH), in which about 72% of TPH was removed. In Phase I, the release of S2- was effectively controlled by the addition of akaganeite. The oxidation of S2- by Fe3+ and the precipitation of S2- by Fe2+ were the main mechanisms for S2- removal. In Phase II, the injection of NO3- completely inhibited the sulfate reduction process. Most of residual AVS and S-0 were removed within 4 weeks after NO3- injection. The 16S rRNA clone library-based analysis revealed a distinct shift of bacterial community structure in the sediment over different treatment phases. The clones affiliated with Desulfobacterales and Desulfuromonadales were the most abundant in Phase I, while the clones related to Thioalkalivibrio sulfidophilus, Thiohalomonas nitratireducens and Sulfurimonas denitrificans predominated in Phase II. (C) 2015 Elsevier Ltd. All rights reserved.
机译:这项研究开发了一种新颖的综合生物修复工艺,用于去除石油碳氢化合物并减轻被污染的海洋沉积物中还原硫所引起的气味。生物修复过程包括两个阶段。在阶段I中,将乙酸盐作为共底物加入沉淀物中,以促进硫酸盐的还原过程。同时,在沉积物的表层中加入了赤铁矿(β-FeOOH),以防止S2-释放到上层海水中。在阶段II中,将NO3-作为电子受体注入沉淀物中,以促进反硝化过程。处理20周后,硫酸盐还原和反硝化过程的顺序整合导致总石油烃(TPH)的有效生物降解,其中约72%的TPH被去除。在阶段I中,通过添加赤霞石可有效控制S2-的释放。 Fe2 +氧化S2-和Fe2 +沉淀S2-是去除S2-的主要机理。在阶段II中,NO3-的注入完全抑制了硫酸盐的还原过程。注入NO3后4周内,大部分残留的AVS和S-0被去除。基于16S rRNA克隆文库的分析揭示了不同处理阶段沉积物中细菌群落结构的明显变化。在第一阶段中,与脱硫细菌和脱硫门单胞菌相关的克隆最丰富,而与硫代嗜盐硫弧菌,硫代硫代嗜盐单胞菌和反硝化硫单胞菌有关的克隆在第二阶段占主导地位。 (C)2015 Elsevier Ltd.保留所有权利。

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