Hu Zhiqiang, Ferraina Richard A, Ericson Jon F, Smets Barth F
Environmental Engineering Program, Department of Civil & Environmental Engineering, University of Connecticut, Storrs, CT 06269-2037, USA.
Water Res. 2005 Sep;39(15):3501-10. doi: 10.1016/j.watres.2005.06.009.
Biodegradation rates of benzoate and related aromatic compounds, 3-nitrobenzoate, 4-chlorobenzoate, 4-chlorophenol, and 2,4-dichlorophenol by unexposed (unacclimated) and long-term exposed (acclimated) biomass were quantified using a modified fed-batch technique. The acclimated biomass was taken after approximately 1-year of operation from three lab-scale sequencing batch reactors (SBR). These reactors were operated under various cycling electron acceptor conditions with a continuous feed of a synthetic wastewater containing biogenic and nonbiogenic chemicals including benzoate, 3-nitrobenzoate, and 4-chlorophenol, but not 4-chlorobenzoate or 2,4-dichlorophenol. The unexposed biomass was taken from a full-scale wastewater treatment plant, which constituted one of the original sources of inoculum for the lab-scale SBRs. The acclimated biomass manifested high removal rates of benzoate and related aromatic compounds with additional removal of structurally similar chemicals (4-chlorobenzoate and 2,4-dichlorophenol). The unacclimated biomass showed no removal of 3-nitrobenzoate, 4-chlorobenzoate or 2,4-dichlorophenol. Addition of biogenic substrates reduced the degradation of most aromatic compounds tested, but it enhanced 2,4-dichlorophenol removal. Biodegradation rates of each aromatic compound with the biomass from the anoxic/aerobic SBR were further determined under anaerobic (absence of aeration and NO3-), anoxic (no aeration, but with surplus NO3-), standard oxygen (DO > 0.2 mg/L), and elevated oxygen (DO > 25 mg/L) conditions. The removal rate of both benzoate and 3-nitrobenzoate decreased under anaerobic condition but not under the anoxic condition; 4-chlorophenol biodegradation, on the other hand, was reduced significantly under both anoxic and anaerobic conditions. The removal rates of aromatic compounds, particularly those of 3-nitrobenzoate and 2,4-dichlorophenol, increased significantly under elevated dissolved oxygen conditions. Our results demonstrated that when the biochemical conditions shifted from oxygen-respiration to nitrate respiration, to anaerobiosis, the biodegradation rates of test aromatic compounds decreased or ceased.
采用改良的分批补料技术,对未接触过(未驯化)和长期接触过(已驯化)的生物质对苯甲酸盐及相关芳香族化合物、3-硝基苯甲酸盐、4-氯苯甲酸盐、4-氯苯酚和2,4-二氯苯酚的生物降解率进行了量化。已驯化的生物质取自三个实验室规模的序批式反应器(SBR)运行约1年后的样本。这些反应器在各种循环电子受体条件下运行,持续进料含生物源和非生物源化学物质的合成废水,这些化学物质包括苯甲酸盐、3-硝基苯甲酸盐和4-氯苯酚,但不包括4-氯苯甲酸盐或2,4-二氯苯酚。未接触过的生物质取自一个全规模污水处理厂,该厂是实验室规模SBR接种物的原始来源之一。已驯化的生物质对苯甲酸盐及相关芳香族化合物表现出较高的去除率,对结构相似的化学物质(4-氯苯甲酸盐和2,4-二氯苯酚)也有额外的去除效果。未驯化的生物质对3-硝基苯甲酸盐、4-氯苯甲酸盐或2,4-二氯苯酚没有去除效果。添加生物源底物降低了大多数测试芳香族化合物的降解,但提高了2,4-二氯苯酚的去除率。在厌氧(无曝气和硝酸盐)、缺氧(无曝气,但有过量硝酸盐)、标准氧(溶解氧>0.2mg/L)和高氧(溶解氧>25mg/L)条件下,进一步测定了来自缺氧/好氧SBR的生物质对每种芳香族化合物的生物降解率。厌氧条件下苯甲酸盐和3-硝基苯甲酸盐的去除率均下降,但缺氧条件下未下降;另一方面,4-氯苯酚在缺氧和厌氧条件下的生物降解均显著降低。在溶解氧升高的条件下,芳香族化合物的去除率,特别是3-硝基苯甲酸盐和2,4-二氯苯酚的去除率显著提高。我们的结果表明,当生化条件从有氧呼吸转变为硝酸盐呼吸,再到厌氧时,测试芳香族化合物的生物降解率会降低或停止。