Alkaline modification of carrageenans. Part III. Use of mild alkaline media and high ionic strengths
The cyclization reaction (formation of 3,6-anhydro-α-D-galactose and 3,6-anhydro-α-D-galactose 2-sulfate units from α-D-galactose 6-sulfate and 2,6-disulfate residues, respectively) of carrageenans follows a pseudo-first-order kinetics. This reaction can be carried out, at reasonable rates, in sodiu...
Guardado en:
Autores principales: | Ciancia, Marina, Matulewicz, María Cristina, Cerezo, Alberto Saúl |
---|---|
Publicado: |
1997
|
Materias: | |
Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01448617_v32_n3-4_p293_Ciancia http://hdl.handle.net/20.500.12110/paper_01448617_v32_n3-4_p293_Ciancia |
Aporte de: |
Ejemplares similares
-
Alkaline modification of carrageenans. Part III. Use of mild alkaline media and high ionic strengths
por: Ciancia, M., et al. -
Effect of ionic strength on the behavior of amperometric enzyme electrodes mediated by redox hydrogels
Publicado: (1999) -
Effect of ionic strength on the behavior of amperometric enzyme electrodes mediated by redox hydrogels
por: Battaglini, F., et al. -
Alkali-modification of carrageenans: mechanism and kinetics in the kappa/iota-, mu/nu- and lambda-series
por: Ciancia, M., et al. -
Alkali-modification of carrageenans: mechanism and kinetics in the kappa/iota-, mu/nu- and lambda-series
por: Ciancia, Marina, et al.
Publicado: (1993)