Study of the Reactivity of Lignin Model Compounds to Fluorobenzylation Using C and F NMR: Application to Lignin Phenolic Hydroxyl Group Quantification by F NMR.

Lignin is an aromatic biopolymer derived from lignocellulosic biomass. Providing a comprehensive structural analysis of lignin is the primary motivation for the quantification of various functional groups, with a view to valorizing lignin in a wide range of applications. This study investigated the lignin fluorobenzylation reaction and performed a subsequent F-NMR analysis to quantify hydroxyl groups, based on a work developed two decades ago by Barrelle et al.

Synthesis and characterization of cellulose carbonate using greenchemistry: Surface modification of Avicel.

The development of new derivatives based on renewable natural resources using green chemistry is a concept gaining recognition in several industries. This work focused on the preparation and characterization of cellulose carbonate using dimethyl carbonate as the green reagent in ethanoic KOH solution. The effect of several reaction parameters were evaluated, i.

Silane adsorption onto cellulose fibers: hydrolysis and condensation reactions.

The hydrolysis of three alkoxysilane coupling agents, gamma-methacryloxypropyltrimethoxysilane (MPS), gamma-aminopropyltriethoxysilane (APS), and gamma-diethylenetriaminopropyltrimethoxysilane (TAS), was carried out in an ethanol/water (80/20) solution and followed by 1H, 13C, and 29Si NMR spectroscopy, which showed that its rate increased in the order MPS < APS < TAS. The formation of the silanol groups was followed by their self-condensation to generate oligomeric structure. APS and MPS only gave soluble products, whereas colloidal particles precipitated in the medium when TAS was hydrolyzed.