Chemical modification of pectin: environmental friendly process for new potential material development (Articolo in rivista)

Type
Label
  • Chemical modification of pectin: environmental friendly process for new potential material development (Articolo in rivista) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1039/C0PY00341G (literal)
Alternative label
  • Monfregola L, Leone M, Vittoria V, Amodeo P, De Luca S (2011)
    Chemical modification of pectin: environmental friendly process for new potential material development
    in Polymer chemistry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Monfregola L, Leone M, Vittoria V, Amodeo P, De Luca S (literal)
Pagina inizio
  • 800 (literal)
Pagina fine
  • 804 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 2 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
  • DOI: 10.1039/C0PY00341G (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Institute of Biostructures and Bioimages, National Research Council, Naples, Italy Department of Chemical and Food Engineering, University of Salerno, Fisciano (SA), Italy Institute of Biomolecular Chemistry, National Research Council, Pozzuoli (NA), Italy (literal)
Titolo
  • Chemical modification of pectin: environmental friendly process for new potential material development (literal)
Abstract
  • Chemical modification of pectin was successfully accomplished as a solvent free process. It involved acylation of alcoholic functions of the polysaccharide by using several fatty acid anhydrides. The reaction was performed by simply mixing the reagents with a catalytic amount of the inorganic base potassium carbonate and heating the obtained mixture at a temperature of 160 °C. The desired esters were fully characterized by NMR and FT-IR spectroscopy. (literal)
  • Chemical modification of pectin was successfully accomplished as a solvent free process. It involved acylation of alcoholic functions of the polysaccharide by using several fatty acid anhydrides. The reaction was performed by simply mixing the reagents with a catalytic amount of the inorganic base potassium carbonate and heating the obtained mixture at a temperature of 160 °C. The desired esters were fully characterized by NMR and FT-IR spectroscopy. (literal)
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