http://www.cnr.it/ontology/cnr/individuo/prodotto/ID18041
Chemiluminescence from oxidation of polyamide 6,6. I. The oxidation of pure polyamide (Articolo in rivista)
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- Label
- Chemiluminescence from oxidation of polyamide 6,6. I. The oxidation of pure polyamide (Articolo in rivista) (literal)
- Anno
- 2003-01-01T00:00:00+01:00 (literal)
- Alternative label
P. Cerruti, C. Carfagna, J. Rychlý, L. Matisová-Rychlá (2003)
Chemiluminescence from oxidation of polyamide 6,6. I. The oxidation of pure polyamide
in Polymer degradation and stability
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- P. Cerruti, C. Carfagna, J. Rychlý, L. Matisová-Rychlá (literal)
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- No. Citazione=6;
Autocitazione=1;
Motore utilizzato per le citazioni=Google Scholar. (literal)
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- CNR, University of Naples Federico II, Slovak Academy of Sciences. (literal)
- Titolo
- Chemiluminescence from oxidation of polyamide 6,6. I. The oxidation of pure polyamide (literal)
- Abstract
- The chemiluminescence (CL) accompanying the oxidation of both polyamide 6,6 and a model diamide with no reactive endgroups is reported. CL emission for neat diamide starts after melting of crystallites, and the shapes of the intensity-time curve show a sigmoidal behaviour, typical of the chain oxidation of organic compounds. Adipic acid shortens induction period of chemiluminescence increase. A bimolecular hydroperoxide decomposition model can successfully describe the kinetic runs of CL. Polyamide 6,6 CL runs are apparently composed of 3 different kinetic stages: a decay from an initial CL value, due to the termination of peroxyl radicals being trapped in the polymer after processing and storage (stage I), a sudden increase of emission, related to depletion of terminal amino groups (stage II), and a major maximum of emission, decaying again to a lower level of chemiluminescence, indicating chain oxidation of -CONH-CH2- structural units (stage III). Terminal carboxyl groups show the general tendency to shift the induction time of the third stage to a shorter time. (literal)
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