Wood modifications are becoming popular as a way to enhance the performance of wood, either to make it more durable, improve the performance of wood, or give it new functionality as a multifunctional or smart material. While wood modifications have been examined since the early 1900s, the topic has become a dominant area of study in wood science over the past decade. This review summarizes recent advances and provides future perspective on a selection of wood modifications, i.e., the methods that are currently commercialized (acetylation, furfurylation, and thermal modification), a rediscovered ancient practice (charring), a family of polymerization modifications that have so far made it to the pilot scale, and examples of novel wood-based functional materials explored at laboratory scale.
Citric acid together with sorbitol (SorCA) have been used to modify wood and improve its properties, such as dimensional stability and biological durability, which partly result from its swelling and sorption behavior. However, the underlying mechanism of water interaction with SorCA-treated wood is very complex and not fully understood. Previous research confirmed cell wall bulking and suggested cross-linking, however the extent of their contribution to moisture-induced changes has not been researched. This study investigated the effect of SorCA treatment on sorption properties of wood in the hygroscopic range (0–95% RH). Scots pine sapwood (Pinus sylvestris L.) was chemically modified with an aqueous SorCA solution at different treatment levels and measured by dynamic vapor sorption (DVS). The observed permanent increase in oven-dry dimensions did not result in a decreased swelling compared to untreated specimens. It was ascribed to the excessive expansion of cell wall matrix caused by a degradation of cell wall constituents by the acidic impregnation solution. However, a reduction in moisture content in comparison to untreated reference was detected. Present findings suggest that the SorCA polyester structure is altered after impregnation inside the wood and affects its sorption behavior by covalent bonding and, presumably, cross-linking with wood polymer constituents.
Cyclic N-methylol compounds such as 1,3-dimethylol-4,5-dihydroxyethyleneurea (DMDHEU) have been used to modify wood and prevent negative effects related to the uptake of moisture. However, the changes in the sorption behavior of wood by treatments with DMDHEU and its derivatives are not fully understood. In the present study, wood blocks were treated with DMDHEU, ether-modified DMDHEU and diethyleneglycolated DMDHEU in order to study the factors that control the changes in moisture uptake in the hygroscopic range (0–95% RH). Dimensional changes of wood blocks during water soaking cycles suggested that the treatments caused a permanent cell wall bulking, whereas the swelling restraint by cross-linking of adjacent cell wall polymers was not permanent. However, the changes in water vapor sorption were not only a result of the cell wall bulking effect that reduced the space in the cell wall to accommodate water. The N-methylol compounds within the wood also provided additional sorption sites, but there was no correlation between absorbed water and accessible OH groups. It was speculated that the co-condensation of the N-methylol compounds with wood polymers had a significant effect on the sorption of the treated wood. At elevated RH, pure resins that were formed by self-condensation took up large quantities of moisture. However, when the N-methylol compounds were heat-cured within the hierarchical structure of wood, the moisture uptake of the treated wood at elevated RH was even lower compared to unmodified wood. Furthermore, the covalent bond formation between wood and resin prolonged the attainment of an equilibrium moisture content.
The importance of thermal modification is increasing worldwide. Increased use of thermally modified timber (TMT) has resulted in a need for reliable quality control, comprising control of variation of the production within defined limits, allowing third-party control in the case of certification and the regulation of customer complaints and claims. Techniques are thus needed to characterise the modification of quality in terms of improved target properties of TMT during industrial production, and of TMT products that have been in service for an arbitrary time. In this study, we aimed to utilise dynamic vapor sorption (DVS) for this purpose. Norway spruce (Picea abies) and European beech (Fagus sylvatica) samples were thermally modified at different temperatures according to different heat treatment techniques: (1) the Silvapro process based on an initial vacuum; (2) an air heat treatment, whereby samples were wrapped in aluminium foil; (3) thermal modification of wood samples in the ambient atmosphere in a laboratory oven. Wood samples from closed processes were analysed for validation. TMT was characterised with respect to mass loss, colour and density. Mass loss of wood due to modification (MLTM) was correlated with factors derived from DVS analysis. The present DVS measurements suggest that the equilibrium wood moisture content (EMC95% RH), the time to reach 10% wood moisture content (t10% MC), and the elongation factor, c, derived from a logarithmic function, can serve as alternative parameters to characterise the quality of several thermal modification processes. Further studies are recommended using other wood species, different modification processes and further parameters gained from DVS measurements to understand the robustness and the predictive power of the applied technique.
Recent studies showed treatments with sorbitol and citric acid (SorCA) to significantly improve the dimensional stability and biological durability of wood. The industrialization of this process requires a quality control (QC) method to determine if the fixated chemicals are homogenously distributed within the piece of wood, which is essential for uniform material performance. Therefore, the objective of this work was to evaluate the use of common electromagnetic radiation-based methods to determine the degree of modification in SorCA-treated wood. Both Fourier transform infrared (FTIR) spectroscopy and near-infrared (NIR) spectroscopy have been used to create rough calibrations for the weight percent gain (WPG) prediction models. The FTIR measurements resulted in a high linear correlation between the band area ratio (BAR) and the WPG (R2 = 0.93). Additionally, a partial least square (PLS) regression of NIR spectroscopic data resulted in a model with a high prediction power (R2 = 0.83). Furthermore, X-ray density profiling emerged as a simple alternative for the QC by showing a gradient of modification chemicals inside the sample and differences in chemical uptake between earlywood and latewood. Overall, it can be concluded that the results from FTIR, NIR and X-ray densitometry can serve as indicators of impregnation chemical distribution in SorCA-modified wood.
Durability-based designs with timber require reliable information about the wood properties and how they affect its performance under variable exposure conditions. This study aimed at utilizing a material resistance model (Part 2 of this publication) based on a dose–response approach for predicting the relative decay rates in above-ground situations. Laboratory and field test data were, for the first time, surveyed globally and used to determine material-specific resistance dose values, which were correlated to decay rates. In addition, laboratory indicators were used to adapt the material resistance model to in-ground exposure. The relationship between decay rates in- and above-ground, the predictive power of laboratory indicators to predict such decay rates, and a method for implementing both in a service life prediction tool, were established based on 195 hardwoods, 29 softwoods, 19 modified timbers, and 41 preservative-treated timbers.