SciELO - Scientific Electronic Library Online

 
vol.54 número5Frustración local en la red arquimediana (3,4,6,4)A resonant nuclear reaction analysis of fluorine in thin CdO films índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Revista mexicana de física

versão impressa ISSN 0035-001X

Resumo

ELIZALDE-TORRES, J. et al. Thermally assisted NO2 and NH3 gas desorption process in a polyaniline thin film based optochemical sensor. Rev. mex. fis. [online]. 2008, vol.54, n.5, pp.358-363. ISSN 0035-001X.

NO2 gas is a strong electron acceptor that can oxidize the chemically deposited semiconductor polyaniline (PANI) at room temperature under atmospheric pressure. Since each redox state of this polymer is associated with a specific electronic structure, an oxidized PANI thin film undergoes a color change that can be detected in a sensitive optochemical sensor. But the strongly absorbed NO2 molecules cannot be removed at room temperature from the polymer material during the purging process with a dried N2 gas flux. We report in this work that a heating element can be integrated into the optochemical sensor to elevate the sensing sample temperature during the desorption process. At temperatures higher than 50° C, the optical signal of the NO2 absorbed PANI samples starts to return to its original value during the purging process, suggesting the desorption of the NO2 species from the PANI samples. The higher the heating temperature, the greater the activation energy for desorption, and consequently the faster the desorption speed. Similar results are also obtained for the NH3 desorption process occurring in the same polymer.

Palavras-chave : Polyaniline thin films; NO2 desorption process; activation energy for desorption; optochemical sensors.

        · resumo em Espanhol     · texto em Inglês     · Inglês ( pdf )

 

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons