ABSTRACT
Lignin-poly(ethylene)glycol diglycidyl ether hydrogels were synthesized from lignin fractions readily extracted during the hot-water treatment of angiosperms: hardwoods, sugar maple and energy-crop willow, monocotyledons, grasses, miscanthus and agriculture residues, and wheat straw. These lignins represent a broad range of chemical structures and properties as a comparative analysis of their suitability to produce the hydrogels as a novel carrier of chaga-silver nanoparticles. The formation of hydrogels was assessed via attenuated total reflectance Fourier-transformed infrared spectroscopy. Then, the hydrogels were observed via scanning electron microscopy and evaluated for their free-absorbency capacity and moduli of compression. Furthermore, a hydrogel produced from kraft lignin and two commercial hydrogels was evaluated to benchmark the effectiveness of our hydrogels. Chaga extracts were prepared via the hot-water extraction of chaga mushroom, a method selected for its relatively higher yields and preserved antioxidizing activities. Hydrogels synthesized with lignins of monocotyledons, wheat straw, and miscanthus were found to be suitable carriers for chaga-silver nanoparticles due to their favorable absorption and release behaviors.
ABSTRACT
A blend of commercial willow cultivars (Salix spp.) was subjected to hydrothermal pretreatment: hot-water extraction in a pilot plant 65-ft3 digester. Lignin recovered from the autohydrolyzate (willow lignin, WL) was used to produce hydrogels and thermoplastic blends. Lignin-kaolin-acrylamide (WL 10.7 % w/w) and lignin-poly(ethylene)glycol diglycidyl ether (WL 66.7 % w/w) hydrogels exhibited favorable adsorption and absorption properties, respectively. Dye adsorption kinetics, swelling capacities, fragrance emanation, and compression moduli were measured for the hydrogels, along with SEM characterization. Additionally, WL was esterified by acetylation (C2 , WAc) and acylation with lauroyl chloride (C12 , WFAE and WFAEH ). The crude and esterified lignin samples were blended (1-12 % w/w) with polylactic acid (PLA) via lab-scale melt extrusion to produce thermoplastic blends. The physicochemical properties of the blends were evaluated. They exhibited an increase in degradation temperature and UV absorbance with potential to hinder photodegradation of PLA and may be leveraged in packaging applications.
