posted on 2019-12-10, 18:44authored byJasmine Viger-Gravel, Wu Lan, Arthur C. Pinon, Pierrick Berruyer, Lyndon Emsley, Michel Bardet, Jeremy Luterbacher
In the continuously developing field of lignocellulosic
biomass,
high-yield lignin depolymerization processes are sought to optimize
its productivity and profitability. Recently, formaldehyde stabilization
during lignin extraction and biomass pretreatment has been found to
drastically enhance subsequent lignin upgradeability but can affect
cellulose digestibility. The exact role and/or form of formaldehyde
on the residual biomass surface is still not fully understood. Here,
we use magic angle spinning (MAS) dynamic nuclear polarization (DNP)
methods to characterize the components that remain inside the residual
cell wall after the lignin extraction process and reveal the topochemistry
of the solid residue. The regioselectivity of relayed DNP allows the
observation of hyperpolarization in a range of 40–200 nm from
the surface of the cell wall for poplar wood materials. That regioselectivity
allows us to distinguish between the external secondary cell wall
and the inner middle lamellae. In that respect, for the untreated
wood, we confirm that there is less lignin in the outer part of the
cell wall than deeper inside. In treated wood, we determine that the
role of dioxane during the process is to enable the extraction of
the modified products from the cell wall. We show that the modified
lignins which were not extracted in the absence of dioxane accumulate
in a 40 nm region at the surface of the cell wall. Also, using carbon-13
enriched formaldehyde during the process, we show that 1% of the total
amount of carbon in the material is assigned to self-polymerization
and that no covalent bonds to cellulose are observed.