Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/478718
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dc.contributor.authorBRUNE, W.pt_BR
dc.contributor.authorFABRIS, J. D.pt_BR
dc.contributor.authorJOSE, S.pt_BR
dc.date.accessioned2011-04-10T11:11:11Zpt_BR
dc.date.accessioned2011-04-10T11:11:11Zpt_BR
dc.date.available2011-04-10T11:11:11Zpt_BR
dc.date.available2011-04-10T11:11:11Zpt_BR
dc.date.created1998-01-21pt_BR
dc.date.issued1988pt_BR
dc.identifier.citationAnais da Academia Brasileira de Ciências, Rio de Janeiro, v. 60, n. 3, p. 255-263, 1988.pt_BR
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/478718pt_BR
dc.descriptionThe complexation of pentacyanoamine ferrate with canavanine is not a specific one. Other amino acids, especially tryptophan and histidine may also react with proper analytical features. Se also do the indolyl and imidazolyl moieties of nonamino acids. Photoactivation does neither seem to occur by exposure of the pentacyanoamine ferrate reagent to daylight, nor is it a perequisite for a more sensitive response of canavanine complexation. On the other hand, oxidants and reducers may well interfere with the absorbance of the complex. In addition molar absorbance, stoichiometric ratio of the complex, and reation-order kinetics were determined. By mean of temperature programming equilibrion constant andreaction kinetics, enthalpy, Gibbs nenergy, entropy values, and activation energy of complex formation were stablished.pt_BR
dc.language.isoporpt_BR
dc.rightsopenAccesspt_BR
dc.titleThe canavanine-pentacyanoamine ferrate complex formation.pt_BR
dc.typeArtigo de periódicopt_BR
dc.date.updated2018-07-18T11:11:11Zpt_BR
dc.subject.thesagroOxido de Ferropt_BR
dc.subject.nalthesaurusironpt_BR
dc.subject.nalthesaurusoxidespt_BR
riaa.ainfo.id478718pt_BR
riaa.ainfo.lastupdate2018-07-18 -03:00:00pt_BR
dc.contributor.institutionEMBRAPA-CNPMS.pt_BR
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