Behavior of alkylphenol polyethoxylate metabolites during soil aquifer treatment

被引:74
|
作者
Montgomery-Brown, J
Drewes, JE
Fox, P
Reinhard, M [1 ]
机构
[1] Stanford Univ, Terman Engn Ctr, Dept Civil & Environm Engn, Stanford, CA 94305 USA
[2] Colorado Sch Mines, Golden, CO 80401 USA
[3] Arizona State Univ, Dept Civil & Environm Engn, Tempe, AZ 85287 USA
关键词
alkylphenol polyethoxylates (APEOs); alkylphenol ethoxycarboxylates (APECs); carboxylated alkylphenol polyethoxycarboxylates; (CAPECs); nonylphenol (NP); soil aquifer treatment (SAT); biodegradation;
D O I
10.1016/S0043-1354(03)00294-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The attenuation of alkylphenol polyethoxylates (APEOs) metabolites was studied at a soil aquifer treatment (SAT) site located in Arizona, USA. Two parcels of water were monitored during infiltration; one parcel was predominantly oxic while the other was predominantly anoxic. In this study, only alkylphenol ethoxycarboxylates (APECs) and carboxyalkylphenol ethoxycarboxylates (CAPECs) were detected, no short-chained APEOs were observed-even under anoxic conditions. APEO metabolites were rapidly (< 7 days) removed under both aerobic and anoxic conditions. In general, the length of the ethoxycarboxylate chain decreases with depth-at depths greater than 3 m, only alkylphenoxy acetic acids (AP1ECs), carboxyalkylphenoxy acetic acids (CAP1ECs), and alkylphenols (APs) remain. Under aerobic conditions, octylphenol and nonylphenol concentrations decreased by similar to 80% (w/w) within 3 m of the ground surface. Under anoxic conditions however, alkylphenol concentrations increased by similar to 200% during the first 1.5 m and then decreased during the next 1.5 m; overall, under anoxic conditions, alkylphenol concentrations increased by similar to 38% within 3 m. During infiltration, APEC and CAPEC concentrations decrease by more than 95% within 3 m of SAT. Alternate flooding and drying cycles appear to enhance overall APEO metabolite removal efficiencies. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3672 / 3681
页数:10
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