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Fate of microconstituents in biosolids composted in an aerated silage bag.

作者信息

Lozano Nuria, Andrade Natasha A, Deng Di, Torrents Alba, Rice Clifford P, McConnell Laura L, Ramirez Mark, Millner Patricia D

机构信息

a Department of Water and Environmental Science and Technology , University of Cantabria , Santander , Cantabria , Spain.

出版信息

J Environ Sci Health A Tox Hazard Subst Environ Eng. 2014;49(6):720-30. doi: 10.1080/10934529.2014.865461.

Abstract

Although most composting studies report pathogen concentrations, little is known about the fate of Endocrine Disruptor Chemicals (EDCs) during composting. In this study, a positively aerated polyethylene bag composting system was filled with a mixture of woodchips and limed biosolids from a large Waste Water Treatment Plant (WWTP) to study the removal efficiency of two different groups of EDCs. Two antibacterial compounds, Triclocarban (TCC) and Triclosan (TCS), and a TCS byproduct, Methyltriclosan (MeTCS), as well as seven congeners of flame retardants known as PBDEs (Polybrominated Diphenyl Ethers) were studied during two phases of composting: 1) a thermophilic phase, in which positive mechanical aeration, pushing air into and through the materials matrix, was conducted for 2 months; and 2) a curing and stabilization phase in which no mechanical aeration was provided and the bag was opened to ambient passive aeration to simulate storage conditions for seven months. Our results showed that while TCC concentrations remained constant, TCS degradation took place during both phases. The degradation of TCS was corroborated by the formation of MeTCS in both phases. The TCS concentrations decreased from 18409 ± 1,877 to 11955 ± 288 ng g(-1) dry wt. during the thermophilic phase and declined from 11,955 ± 288 to 7,244 ± 909. ng g(-1) dry wt. by the end of the curing phase. Thus, slightly greater TCS transformation occurred during the second than during the first (35.1 vs. 39.4%). MeTCS concentrations increased from 189.3 ± 8.6 to 364.6 ± 72.5 ng g(-1) dry wt. during the first phase and reached 589.0 ± 94.9 ng g(-1) dry wt. at the end of the second phase. PBDEs concentrations were below quantification limits for all but two of the congeners analyzed (BDE-47 and BDE-99). PBDE concentrations were measured at the end of the first phase only and were comparable to initial concentrations.

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