4.8 Article

Distribution and behavior of nonylphenol, octylphenol and nonylphenol monoethoxylate in okyo metropolitan area: Their association with aquatic particles and sedimentary distributions

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 35, Issue 6, Pages 1041-1049

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/es001250i

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Distributions of alkylphenols (APs) [i.e., nonylphenol (NP) octylphenol (OP)], and nonylphenol monoethoxylate (NP1EO) in wastewater effluents, river water, and riverine and bay sediments in the Tokyo metropolitan area were demonstrated. During sewage treatments, NP and OP were efficiently removed from the sewage effluents through activated sludge treatments. Greater removal for NP (93% on average) than OP (84% on average) was consistent. with their partitioning behavior to particles in primary and secondary effluents. NP concentrations in the river water samples ranged from 0.051 to 1.08 mug/L with higher concentrations in summer and spring than iii colder seasons. In the river water samples; similar to 20% of NP was found in the particulate phase. Organic. carbon-normalized apparent partition coefficients (K'(oc)) for NP (10(5.22 +/- 0.38)) and OP (10(4.65) (+/- 0.42)) Were 1 Order of magnitude higher than those expected from their octanol-water partition coefficients (K-ow), indicating strong affinity of APs tol aquatic particles. Among NP isomers, no significant differences in their K'(oc) values were suggested. This is consistent with surprisingly uniform isomer peak profiles among the technical standard and all the environmental samples analyzed. NP and OP were widely distributed in the river sediments in Tokyo, and relatively high concentrations (0.5-13.0 mug/g dry) of NP were observed in a long reach (similar to 10 km) in the Sumidagawa River. In situ production of APs in the river sediment was suggested. Seaward dec rea sing trend in APs concentration was observed from the estuary to the Tokyo Bay. APs were well preserved in a sediment core collected from the bay. The profile shows subsurface maximum of AP concentrations in the layer deposited around the mid-1970s. The recent decrease in AP concentrations can be attributed to the legal regulation of industrial wastewater in the early 1970s.

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