F. J. Santiago-Medina1, A. Pizzi1, 2*, M. C. Basso1, L. Delmotte3, S. Abdalla2
Journal of Renewable Materials, Vol.5, No.5, pp. 388-399, 2017, DOI:10.7569/JRM.2017.634142
Abstract The reaction of a desulphurized kraft lignin with hexamethylene diamine as a model of a polyamine has been investigated. For this purpose, guaiacol was also used as a lignin model compound and treated under similar conditions. Solid state CP-MAS 13C NMR, FTIR and MALDI-TOF spectroscopy studies revealed that polycondensation compounds leading to resins were obtained by the reaction of the amines with the phenolic and aliphatic hydroxy groups of lignin. Simultaneously a second reaction leading to the formation of ionic bonds between the same groups occurred. These new reactions have been clearly shown to involve More >
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