Subramaniam group research featured on cover of ACS Industrial & Engineering Chemistry Research
The research team of Nakisha Mark, Sandip Singh, Anoop Uchagawkar, Erik Hagberg, Thomas Binder and Bala Subramaniam have published their work entitled, "Impacts of Sulfur Impurity and Acid Pretreatment on Catalytic Depolymerization of Corn Cob Lignin" in the April 16 issue of Industrial & Engineering Chemistry Research.
ABSTRACT: When fractionating corn cobs using the acetosolv process, the type of acid catalyst and their concentrations significantly affect the structure of the resulting lignin fraction, as well as its catalytic deconstruction to aromatic monomers. Gel permeation chromatography (GPC) results show that the average molecular weight (∼55,750 g/mol) of the sulfuric acid-pretreated corn cob lignin (H2SO4-CCL) is much greater than that (∼39,400 g/mol) of hydrochloric acid-pretreated CCL (HCl-CCL) at similar acid concentrations, suggesting increased condensation reactions when using sulfuric acid. Furthermore, a significant amount of bound sulfur content (∼2900 ppm) was measured in H2SO4-CCL. This sulfur presence poisons the Pd/C catalyst used in the downstream catalytic conversion of the lignin in methanol to form monolignols and derivatives thereof. X-ray photoelectron spectroscopy (XPS) results reveal the presence of both sulfide and sulfate groups on the surface Pd sites, rendering them inactive and amenable to possible leaching. Elemental mapping of spent catalysts using scanning transmission electron microscopy-high angle annular dark field (STEM-HAADF)/energy-dispersive X-ray (EDX) technique corroborate the overlapping presence of Pd, S, and O in the micrographs. 2D 1H/13C HSQC nuclear magnetic resonance (NMR) spectroscopy reveals that the use of H2SO4 preserves aryl ether linkages only at low concentrations. In contrast, the use of HCl in the acetosolv process preserves such linkages even at higher concentrations while also mitigating sulfur poisoning of the Pd/C catalyst. Consequently, the yield of aromatic monomers during catalytic fractionation of HCl-CCL was doubled compared to that of H2SO4-CCL under identical operating conditions.