Improving the environmental performance of resins in wood treatment by using renewable chemicals has been a topic of interest for a long time. At the same time, lignin, the second most abundant biomass on earth, is produced in large scale as a side product and mainly used energetically. The use of lignin in wood adhesives or for wood modification has received a lot of scientific attention. Despite this, there are only few lignin-derived wood products commercially available. This review provides a summary of the research on lignin application in wood adhesives, as well as for wood modification. The research on the use of uncleaved lignin and of cleavage products of lignin is reviewed. Finally, the current state of the art of commercialization of lignin-derived wood products is presented.
A newly developed thermo-hydro treatment (THT) for use in a one-stage heat treatment process was examined by focusing on the form stability-related properties of European aspen (Populus tremula), birch silver (Betula pendula), and gray alder (Alnus incana). In particular, wood specimens were subjected to THT in a saturated steam atmosphere in a pilot-scale autoclave heated between 140 and 180°C for 1-3 h. Several parameters of untreated and treated samples after several soaking and drying cycles were compared, namely, the changes in the volumetric swelling, swelling in the radial and tangential directions, cell wall total water capacity, and antiswelling efficiency (ASE). Due to repeated wetting in the cyclic water submersion-drying test, the original ASE of 73% decreased to 65% (180°C for 1 h), and the original ASE of 33% decreased to 5% (140°C for 1 h). Wood modified at 170°C presented good results that were not significantly lower than wood treated at higher temperatures while consuming less energy to deliver ASE improvement and was selected as optimum. To increase the ASE by 1%, the amount of energy consumed was decreased by 41%, 39%, and 17% compared with the treatment regimes of 160°C for 1 h, 160°C for 3 h, and 180°C for 1 h, respectively. The new THT regime led to improved long-term dimensional stability due to the cross-linking of cell wall polymers, which resulted in increased cell wall rigidity.
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