Use of Renewable Alcohols in Autocatalytic Production of Aspen Organosolv Lignins.

This study aimed to investigate the intrinsic efficiency of renewable alcohols, applied under autocatalytic conditions, for removing lignin from aspen and hot-water-extracted aspen while substantially preserving the lignin structure so as to facilitate various valorization strategies. Ethylene glycol (EG), propylene glycol (PG), 1,4-butanediol (BDO), ethanol (EtOH), and tetrahydrofurfuryl alcohol (THFA) were evaluated based on their lignin solubilization ability, expressed as the relative energy difference (RED) following the principles of the Hansen solubility theory. The findings indicate that alcohols with a higher lignin solubilization potential lead to increased delignification, almost 90%, and produce a lignin with a higher content of β-O-4 bonds, up to 68% of those found in aspen milled wood lignin, thereby indicating their potential for valorization through depolymerization.

Grafting PEG on cellulose nanocrystals via polydopamine chemistry and the effects of PEG graft length on the mechanical performance of composite film.

In this study, cellulose nanocrystals (CNCs) with PEG grafts of various lengths (1 k, 2 k, 5 k, and 10 kDa) were prepared via a polydopamine (PDA) mediated method in the aqueous solution. The prepared CNC-PEGs were further used to reinforce the polyvinyl alcohol (PVA) at the loading of 0, 1, 3, 5, and 7 wt% in order to demonstrate the effects of the PEG length on the properties of the PVA/CNC nanocomposites. PEG surface modification resulted in simultaneous improvements in stiffness and toughness.

A Review of Wet Compounding of Cellulose Nanocomposites.

Cellulose nanomaterials (CNs) are an emerging class of materials with numerous potential applications, including as additives or reinforcements for thermoplastics. Unfortunately, the preparation of CNs typically results in dilute, aqueous suspensions, and the lack of efficient water removal methods has hindered commercialization. However, water may also present opportunities for improving overall efficiencies if its potential is better understood and if it is better managed through the various stages of CN and composite production.

PHBV-graft-GMA via reactive extrusion and its use in PHBV/nanocellulose crystal composites.

Reactive extrusion was used for dicumyl peroxide (DCP)-initiated grafting of glycidyl methacrylate (GMA) to poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV). The effects of GMA and DCP content and their weight ratio on the GMA grafting percentage (GP%), the polymer melt viscosity, and the PHBV molecular weight were investigated. FTIR spectroscopy determined that the DCP did indeed initiate GMA grafting.

Spatially resolved characterization of cellulose nanocrystal-polypropylene composite by confocal Raman microscopy.

Raman spectroscopy was used to analyze cellulose nanocrystal (CNC) -polypropylene (PP) composites and to investigate the spatial distribution of CNCs in extruded composite filaments. Three composites were made from two forms of nanocellulose (CNCs from wood pulp and the nano-scale fraction of microcrystalline cellulose) and two of the three composites investigated used maleated PP as a coupling agent. Raman maps, based on cellulose and PP bands at 1098 and 1460 cm(-1), respectively, obtained at 1 μm spatial resolution showed that the CNCs were aggregated to various degrees in the PP matrix.