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Lignins as macromonomers for polyurethane synthesis: a comparative study on hydroxyl groups determination

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Resumo:The hydroxyl group contents of four technical lignins [Indulin AT (Meadwestvaco), Alcell (Repap), Curan 27-11P (Borregaard LignoTech), and Sarkanda (Granit SA)] were investigated in view of their valorization as polyols in polyurethane synthesis. The different hydroxyl group contents were determined by the following methods: titration and 1H-NMR, 13C-NMR, and 31P-NMR spectroscopy. The titration method chosen was on the basis of a standard method commonly used to characterize commercial polyols for polyurethanes synthesis. The values of the total and phenolic hydroxyl contents determined by the different techniques were found to be in good agreement. For the total hydroxyl contents, coefficients of variation of 5.6% (Alcell), 3.2% (Indulin AT), 2.3% (Sarkanda), and 6.2% (Curan 27-11P) were established. For the phenolic hydroxyl contents, a good correlation was observed between data obtained from 31P-NMR and 13C-NMR for all lignin samples, except for the Sarkanda lignin, for which a relatively high coefficient of variation (12.6%) was found. For softwood lignins (Indulin AT and Curan 27-11P), the phenolic hydroxyl content determined by 1H-NMR was always lower than that deduced from 31P-NMR and 13C-NMR spectroscopy.
Autores principais:Cateto, Carolina
Outros Autores:Barreiro, M.F.; Rodrigues, Alírio; Brochier-Salon, M.C.; Thielemans, Wim; Belgacem, Mohamed Naceur
Assunto:NMR Polyurethanes Renewable resources
Ano:2008
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso restrito
Instituição associada:Instituto Politécnico de Bragança
Idioma:inglês
Origem:Biblioteca Digital do IPB
Descrição
Resumo:The hydroxyl group contents of four technical lignins [Indulin AT (Meadwestvaco), Alcell (Repap), Curan 27-11P (Borregaard LignoTech), and Sarkanda (Granit SA)] were investigated in view of their valorization as polyols in polyurethane synthesis. The different hydroxyl group contents were determined by the following methods: titration and 1H-NMR, 13C-NMR, and 31P-NMR spectroscopy. The titration method chosen was on the basis of a standard method commonly used to characterize commercial polyols for polyurethanes synthesis. The values of the total and phenolic hydroxyl contents determined by the different techniques were found to be in good agreement. For the total hydroxyl contents, coefficients of variation of 5.6% (Alcell), 3.2% (Indulin AT), 2.3% (Sarkanda), and 6.2% (Curan 27-11P) were established. For the phenolic hydroxyl contents, a good correlation was observed between data obtained from 31P-NMR and 13C-NMR for all lignin samples, except for the Sarkanda lignin, for which a relatively high coefficient of variation (12.6%) was found. For softwood lignins (Indulin AT and Curan 27-11P), the phenolic hydroxyl content determined by 1H-NMR was always lower than that deduced from 31P-NMR and 13C-NMR spectroscopy.