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005     20210129215243.0
024 7 _ |a 10.1016/j.chemosphere.2015.02.031
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024 7 _ |a 0045-6535
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024 7 _ |a 1879-1298
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037 _ _ |a FZJ-2015-02096
082 _ _ |a 333.7
100 1 _ |a Zhu, Linyan
|0 P:(DE-Juel1)156394
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245 _ _ |a An efficient laboratory workflow for environmental risk assessment of organic chemicals
260 _ _ |a Amsterdam [u.a.]
|c 2015
|b Elsevier Science
336 7 _ |a Journal Article
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520 _ _ |a In this study, we demonstrate a fast and efficient workflow to investigate the transformation mechanism of organic chemicals and evaluate the toxicity of their transformation products (TPs) in laboratory scale. The transformation process of organic chemicals was first simulated by electrochemistry coupled online to mass spectrometry (EC–MS). The simulated reactions were scaled up in a batch EC reactor to receive larger amounts of a reaction mixture. The mixture sample was purified and concentrated by solid phase extraction (SPE) for the further ecotoxicological testing. The combined toxicity of the reaction mixture was evaluated in fish egg test (FET) (Danio rerio) compared to the parent compound. The workflow was verified with carbamazepine (CBZ). By using EC–MS seven primary TPs of CBZ were identified; the degradation mechanism was elucidated and confirmed by comparison to literature. The reaction mixture and one primary product (acridine) showed higher ecotoxicity in fish egg assay with 96 h EC50 values of 1.6 and 1.0 mg L−1 than CBZ with the value of 60.8 mg L−1. The results highlight the importance of transformation mechanism study and toxicological effect evaluation for organic chemicals brought into the environment since transformation of them may increase the toxicity. The developed process contributes a fast and efficient laboratory method for the risk assessment of organic chemicals and their TPs.
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700 1 _ |a Santiago-Schübel, Beatrix
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700 1 _ |a Xiao, Hongxia
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700 1 _ |a Thiele, Björn
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700 1 _ |a Zhu, Zhiliang
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700 1 _ |a Qiu, Yanling
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700 1 _ |a Hollert, Henner
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700 1 _ |a Küppers, Stephan
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773 _ _ |a 10.1016/j.chemosphere.2015.02.031
|g Vol. 131, p. 34 - 40
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|t Chemosphere
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|y 2015
|x 0045-6535
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