http://www.cnr.it/ontology/cnr/individuo/prodotto/ID42234
CHLORINATED HERBICIDE (TRIALLATE) DEHALOGENATION BY IRON POWDER (Articolo in rivista)
- Type
- Label
- CHLORINATED HERBICIDE (TRIALLATE) DEHALOGENATION BY IRON POWDER (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.chemosphere.2004.06.040 (literal)
- Alternative label
VOLPE A., LOPEZ A., MASCOLO G., DETOMASO A. (2004)
CHLORINATED HERBICIDE (TRIALLATE) DEHALOGENATION BY IRON POWDER
in Chemosphere
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- VOLPE A., LOPEZ A., MASCOLO G., DETOMASO A. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- VOLPE A.: Consiglio Nazionale delle Ricerche, Istituto di Ricerca Sulle Acque, Sezione di Bari, Via Francesco De Blasio, 5-70123 Bari, Italy
LOPEZ A.: Consiglio Nazionale delle Ricerche, Istituto di Ricerca Sulle Acque, Sezione di Bari, Via Francesco De Blasio, 5-70123 Bari, Italy
MASCOLO G.: Consiglio Nazionale delle Ricerche, Istituto di Ricerca Sulle Acque, Sezione di Bari, Via Francesco De Blasio, 5-70123 Bari, Italy
DETOMASO A.: Consiglio Nazionale delle Ricerche, Istituto di Ricerca Sulle Acque, Sezione di Bari, Via Francesco De Blasio, 5-70123 Bari, Italy (literal)
- Titolo
- CHLORINATED HERBICIDE (TRIALLATE) DEHALOGENATION BY IRON POWDER (literal)
- Abstract
- The reductive degradation of a chlorinated herbicide by iron powder was investigated at lab scale. The studied substrate was triallate (S-2,3,3-trichloroallyl di-isopropyl thiocarbamate) which contains a trichloroethylene moiety potentially reducible by zero-valent iron. Degradation reactions were carried out in batch, at 25 °C, in the absence of oxygen, by contacting electrolytic iron powder (size range: 20-50 um) with a triallate aqueous solution (2.5 mg l-1). Herbicide decay, corresponding evolutions of TOC, TOX and chloride ion release were regularly monitored throughout the reactions. Furthermore, the main degradation by-products were identified by HPLC/MS. The results showed that, after 5 days, herbicide degradation extent was about 97% and that the reaction proceeded through the formation of a dechlorinated alkyne by-product (S-2-propinyl di-isopropyl thiocarbamate) resulting from the complete dechlorination of triallate. The subsequent reduction of such an alkyne intermediate gave S-allyl di-isopropyl thiocarbamate as main end by-product. The identified y-products suggested that dechlorination took place mainly via reductive b-elimination. However, as traces of dichloroallyl di-isopropyl thiocarbamate were also detected, a role, although minor, was assigned even to hydrogenolysis in the overall dechlorination process. (literal)
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