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1.
Environ Pollut ; 158(2): 592-8, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19767134

RESUMO

This paper studies the degradation reactions that 4-chloroaniline can naturally undergo in waters for the action of sun light. 10.00 mg L(-1) 4-chloroaniline aqueous solution, without any addition of organic solvent, are undergone to photoirradiation under conditions that simulate sun light. The degradation pathway, followed by HPLC-DAD-MS/MS methods, is complex since the pollutant gives rise to many photoproducts: the predominant species are characterized by m/z values of 217 (P5) and 218 (P6) and are compatible with dimeric structures of 4-chloroaniline. Vibrio fischeri tests indicate that the photoproducts of 4-chloroaniline are characterized by a toxicity level significantly greater than the precursor.


Assuntos
Compostos de Anilina/química , Compostos de Anilina/toxicidade , Recuperação e Remediação Ambiental/métodos , Luz Solar , Poluentes Químicos da Água/química , Aliivibrio fischeri/efeitos dos fármacos , Cromatografia Líquida de Alta Pressão/métodos , Oxigênio/análise , Espectrometria de Massas em Tandem/métodos , Testes de Toxicidade
2.
J Am Soc Mass Spectrom ; 19(8): 1221-9, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18571428

RESUMO

The paper studies, with the help of HPLC-DAD-MS/MS technique, the hydrolytic and photoinduced degradation processes that take place in aqueous solutions of tribenuron methyl, both when preserved in the dark and when undergoing solar box irradiation under conditions that simulate sun light. The results indicate that the degradation products formed by hydrolysis alone and by photoirradiation are the same, but kinetics of the hydrolysis reaction is much slower. The degradation products are identified as 2-methoxy-4-methylamino-6-methyl-1,3,5-triazine (P1), methyl 2-aminosulfonylbenzoate (P2), and saccharin (P3) and quantified. Ecotoxicological biotests performed on 0.1 microg L(-1) photoirradiated solutions of the herbicide give a border line toxicity situation comparable to that of the precursor and indicate that the herbicide is characterized by low persistence in the environment, as required. Its degradation, however, does not lead to mineralization but to the formation of products of comparable toxicity. To evaluate the matrix effects, the photodegradation of the herbicide is also studied in the presence of rice paddy waters: the process is slower than in ultrapure water but leads to the same products. Experiments performed for comparison by irradiating ultrapure water solutions with UV lamp (254 nm) show that the degradation process is not only faster with respect to sunlight, but gives a different pathway, without in anyway leading to mineralization.


Assuntos
Sulfonatos de Arila/química , Herbicidas/química , Agricultura , Sulfonatos de Arila/efeitos da radiação , Cromatografia Líquida de Alta Pressão , Escuridão , Herbicidas/efeitos da radiação , Hidrólise , Cinética , Luz , Espectrometria de Massas , Oryza , Oxigênio/química , Resíduos de Praguicidas/análise , Fotoquímica , Soluções , Luz Solar , Raios Ultravioleta , Poluentes Químicos da Água/análise
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