Literature DB >> 12409247

Photodegradation of 1-nitropyrene in solution and in the adsorbed state.

Alexander Muck1, Pavel Kubát, Anabela Oliveira, Luis Filipe Vieira Ferreira, Josef Cvacka, Svatopluk Civis, Zdenek Zelinger, Jirí Barek, Jirí Zima.   

Abstract

The photodegradation of the 1-nitropyrene (NPy) has been studied using conventional (Xe and medium pressure Hg lamps) and laser sources (XeCl excimer and Nd-YAG UV). Low energy monochromatic light sources were used to study the early stages of degradation (up to 50% conversion). The medium pressure Hg lamp was used for longer periods of irradiation (up to 6h) and for greater degradation of NPy. The results of our work confirm that degradation occurs by radical mechanism. Aromatic hydroxymethyl, methoxy, hydroxy and nitroso derivatives of pyrene (Py) are created by low energy UV irradiation. After a massive UV irradiation, the Py aromatic system is destroyed and more polar low-molecular compounds are generated. The photochemical method described in this paper, based on irradiation by UV lamp, is therefore, suitable for degradation of fused benzene ring(s) and thus should also be effective for degradation of other nitrated polycyclic aromatic compounds.

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Year:  2002        PMID: 12409247     DOI: 10.1016/s0304-3894(02)00120-6

Source DB:  PubMed          Journal:  J Hazard Mater        ISSN: 0304-3894            Impact factor:   10.588


  2 in total

1.  Photodegradation mechanisms of 1-nitropyrene, an environmental pollutant: the effect of organic solvents, water, oxygen, phenols, and polycyclic aromatics on the destruction and product yields.

Authors:  Zulma I García-Berríos; Rafael Arce
Journal:  J Phys Chem A       Date:  2012-03-29       Impact factor: 2.781

2.  Biotransformation of nitro-polycyclic aromatic compounds by vegetable and fruit cell extracts.

Authors:  Bo Xie; Jun Yang; Qing Yang
Journal:  J Zhejiang Univ Sci B       Date:  2012-04       Impact factor: 3.066

  2 in total

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