Lignin'nin Biyo-Bazlı Dietil Maleat'a Oksidatif Parçalanması İçin USY Zeolit Desteği Üzerinde Fe Türlerinin Mühendisliği

Özet (abstract)

Abstract The development of sustainable routes for polymer monomers is crucial for the chemical industry. Herein, we report a highly efficient and selective oxidative depolymerization strategy for converting lignin into diethyl maleate (DEM), a valuable precursor for polyaspartic polyurea resins. A series of iron oxide catalysts supported on commercial USY zeolites via a simple impregnation-calcination method were developed. Notably, the catalyst prepared using iron sulfate (Fe2(SO4)3) as the precursor exhibited superior performance, achieving a maximum DEM yield of 53.0 wt % and a selectivity of 72.4% from organosolv bagasse lignin, outperforming the iron nitrate- and chloride-derived catalysts by 29.2 and 31.9 wt % in yield, respectively. Comprehensive characterizations revealed that the unique highly dispersed Fe(SO4)x phases significantly increased the proportion of Fe3+ species and facilitated electron transfer across the support-iron interface. The synergistic interplay between sulfur-induced Brønsted acid sites and isolated octahedral iron sites was identified as the key factor driving the efficient cleavage of lignin linkages and subsequent oxidative ring-opening. By combining commercially available supports and earth-abundant metals, this work offers an environmentally viable pathway for lignin depolymerization into polymer monomers, demonstrating significant potential for industrial scalability.

Yazarların özeti; kaynağından alınmıştır. ACS Sustainable Chemistry & Engineering, 2026 · DOI ↗