Electron microscopy (EM) is a key tool for studying the microstructure of wood; however, observing uncoated samples poses a challenge due to surface charging. This study aims to identify the critical voltage that allows for the effective observation of uncoated wood samples without significant loading. As part of the experiment, samples of different wood species were tested, including Acacia (Robinia pseudoacacia L.), Oak (Quercus robur L.), Maple (Acer pseudoplatanus spp.), Ash (Fraxinus excelsior L.), Spruce (Picea abies (L.) Karst.), Thermowood (Thermal modifed Spruce), Garapa (Apuleia leiocarpa), Ipé (Handroanthus spp.), Merbau (Intsia bijuga), and Massaranduba (Manilkara spp.). Several methods were tested for surface preparation for SEM analysis, including the use of a circular saw, a hand milling machine, and a microtome. The results show that the optimal voltage for observing uncoated wood samples varied depending on the wood species. Regarding the selection of wood species and the results obtained, it was found that uncoated samples could be effectively observed. This finding suggests that practical observations can be accelerated and more cost-effective, as all wood species exhibited the required voltage range of 1 kV to 1.6 kV. Additionally, it was determined that using a secondary electron detector was optimal for such observations, as it provided a sufficiently strong signal even at relatively low voltages. Conversely, when using a backscattered electron detector, it was more beneficial to use coated samples to achieve a sufficient signal at higher voltages. This study brings new knowledge that will facilitate further research and applications of electron microscopy in the study of other wood species or wood-based materials.

Cutting beech plywood using abrasive water jet (AWJ) technology represents a significant area of research due to increasing demands for precision, quality, and environmental sustainability in manufacturing processes within the woodworking industry. AWJ technology enables non-contact cutting of materials without causing thermal deformation or mechanical damage, which is crucial for preserving the structural integrity and mechanical properties of the plywood. This article investigates cutting beech plywood using technical methods using an abrasive water jet (AWJ) at 400 MPa pressure, with Australian garnet (80 MESH) as the abrasive material. It examines how abrasive mass flow rate, traverse speed, and material thickness affect AWJ lag, which in turn influences both cutting quality and accuracy. Measurements were conducted with power abrasive mass flow rates of 250, 350, and 450 g/min and traverse speeds of 0.2, 0.4, and 0.6 m/min. Results show that increasing the abrasive mass flow rate from 250 g/min to 350 g/min slightly decreased the AWJ cut width by 0.05 mm, while further increasing to 450 g/min caused a slight increase of 0.1 mm. Changes in traverse speed significantly influenced cut width; increasing the traverse speed from 0.2 m/min to 0.4 m/min widened the AWJ by 0.21 mm, while increasing it to 0.6 m/min caused a slight increase of 0.18 mm. For practical applications, it is recommended to use an abrasive mass flow rate of around 350 g/min combined with a traverse speed between 0.2 and 0.4 m/min when cutting beech plywood with AWJ. This balance minimizes jet lag and maintains high surface quality comparable to conventional milling. For thicker plywood, reducing the traverse speed closer to 0.2 m/min and slightly increasing the abrasive flow should ensure clean cuts without compromising surface integrity.

AbstractSurface pretreatment significantly influences the hygroscopic behavior of wood, which in turn affects surface stability when exposed to variable climatic conditions. This study focuses on how different surface pretreatment methods impact the performance of protective coating applied on spruce wood (Picea abies (L.) Karst.) during one year of natural weathering. Samples were prepared using various surface treatments: milling and sanding with grit sizes P40, P80, and P120, respectively. Two types of coatings were applied: a solventborne coating (ADLER Pullex Plus-Lasur) and a waterborne coating (DColor FK 47 UV Protect). The samples were exposed for 12 months at an outdoor testing site in Suchdol, Czech. Surface properties were assessed through color changes in the CIE Lab* space, gloss measurements (ISO 2813), contact angle analysis, and visual inspection. The results showed that exposure to UV radiation and microbial activities led to the gradual degradation of the optical properties and aesthetic appearance of the wood. Surfaces with greater roughness preserved their aesthetic properties more effectively, indicating a higher absorption of the coating. Untreated wood exhibited low water repellency, while the coated surface demonstrated enhanced hydrophobicity. Notably, the waterborne coating showed a temporary increase in contact angle around the sixth month, indicating surface clogging by dust particles. In contrast, the solventborne coating had a rapid decrease in wettability during the first nine months. These findings suggested the importance of surface pretreatment and coating type in maintaining the long-term performance and aesthetic appearance for wood used in exterior conditions.

The sawmill industry generates substantial waste in the form of wood chips, shavings, and sawdust, which can be repurposed to manufacture particleboards. Conventional particleboards rely on formaldehyde-based adhesives, posing health risks due to formaldehyde emissions. Seeking alternatives, this study explored a bio-based adhesive system composed of citric acid and sorbitol (10 wt%) combined with 0–20 wt% fire retardants (imidazolium-based ionic liquid or ammonium dihydrogen phosphate) for particleboards made from residual sawmill processing. The objective was to assess the efficacy of the adhesive system in enhancing fire retardancy, moisture resistance, and mechanical properties of particleboards. Results indicate that incorporating ammonium dihydrogen phosphate significantly improves fire retardancy, evidenced by limiting oxygen index values of 50–78% and a thickness swelling after water immersion of 9.7%. However, with an internal bonding strength of max 0.24 MPa and modulus of rupture of max 4.3 MPa, the bio-based boards fell short of meeting standard requirements. Future research should focus on optimising the general citric acid and sorbitol-based adhesive formulations to overcome this limitation. Achieving sustainability and safety standards in particleboard production remains a critical objective for future research and industry implementation.

Waste biomass presents both environmental challenges and opportunities for sustainable innovation. Converting biomass into biochar provides an environmentally sustainable method for waste valorization, with biochar demonstrating considerable potential for enhancing fire safety in various material applications. This study examines the fire performance of various biomass feedstocks (reed pellets, olive pits, wood chips, rubber waste) and their corresponding biochars, produced at 700 °C, using cone calorimeter tests. The biomass samples exhibited peak heat release rates (PHRR) ranging from 200 to 600 kW/m2, whereas the PHRR of their biochars was significantly lower, ranging from 20 to 35 kW/m2. Biochar derived from lignocellulosic biomass demonstrated more prolonged combustion behavior, with higher PHRR values, whereas rubber waste biochar exhibited the lowest PHRR (21.3 kW/m2) and total heat release (THR) (4.1 MJ/m2), highlighting its enhanced fire safety compared to its biomass counterpart. The composition of the parent biomass plays a crucial role in determining the biochar’s fire performance. These findings offer valuable insights into the selection of biochar for various applications, particularly as a filler in flame-retardant composites.

Wood densification itself does not, in general, improve the fire-retardant properties sufficiently to reach the standard requirements. The object of this study was to enhance the fire-retardant properties of thermo-mechanically densified wood without any loss of moisture stability and hardness. Scots pine sapwood was pretreated before densification by impregnation with a fire retardant (FR) consisting of ammonium dihydrogen phosphate and urea and then cured in-situ by hot pressing at 150 °C or 210 °C. Densified specimens without FR were used as a control. Set-recovery, fire retardancy in an open flame test, and Brinell hardness were determined. The set-recovery was slightly reduced as a result of the FR treatment, but the pressing temperature and time had a much greater influence. In the open flame test, specimens without FR-treated ignited within 15-50s of exposure to the flame, whereas all the FR-treated specimens exhibited ignition resistance over the 10 minutes duration of the test. Water-soaking cycles had no impact on the ignition resistance in these groups, indicating a strong resistance to water leaching of FR after pressing at 210 °C for 60 minutes. The hardness increased due to the presence of FR after pressing at 210 °C, but sharply decreased after water immersion.

Wood, a fundamental material in construction, confronts durability and weathering challenges, notably UV-induced degradation leading to colour changes. This study investigated a novel treatment using citric acid and urea to enhance the UV stability of wood. The reaction between these compounds generates water-soluble fluorescent species and insoluble particles upon thermal treatment which may provide wood with UV protection. Specimens were treated with two different treatment methods and then exposed to 2016 h of accelerated weathering, during which colour was measured regularly. Citric acid and urea were either pressure impregnated into the wood and thermally reacted in situ during heat treatment or pre-reacted in the absence of wood with subsequent implementation into melamine formaldehyde (MF) and water-based surface coatings. The results showed that water-soluble fluorophore compounds were formed with both treatment methods. Accelerated weathering tests revealed significant colour changes over time, where specimens coated with a mixture of MF and fluorescent particles from the reaction between citric acid and urea, exhibiting the least alteration. The lowest colour change ΔE of 5.9 was observed for specimens coated with a MF-based coating containing 1 wt% of citric acid and urea thermally pre-reacted at a temperature of 180 °C, showcasing potential wood protection applications.

The rise in energy consumption and the increase in the use of bio-based materials in the building sector, has led to the need to investigate the possibilities to use wood as a porous support material for phase change materials (PCMs), and thereby creating a thermal regulative wood-based product. This study investigated the influence of Kraft lignin-glyoxal prepolymer on the thermal-energy storage properties of wood modified with paraffin-type of PCM. The implementation of the modified wood involves preparing PCM emulsions, synthesising lignin-glyoxal prepolymer, and modifying wood with the PCM-Kraft lignin-glyoxal emulsion through vacuum-pressure impregnation. The infrared imaging suggested the ability of PCM-modified wood to delay the temperature changes, even with the introduction of Kraft lignin-glyoxal prepolymer. In conclusion, it is feasible to introduce thermal-energy storage property into wood with the addition of Kraft lignin-glyoxal prepolymer. Further studies will focus on the long-term thermal storage performance properties when this PCM system is subjected to repeated heating/cooling cycles. 

In this study, Kraft lignin was modified by ammonium dihydrogen phosphate (ADP) and urea for achieving phosphorylation and carbamylation, aiming to protect wood against biological and fire attack. Scots pine (Pinus sylvestris L.) sapwood was impregnated with a water solution containing Kraft lignin, ADP, and urea, followed by heat treatment at 150 °C, resulting in changes in the properties of the Kraft lignin as well as the wood matrix. Infrared spectroscopy, 13C cross-polarisation magic-angle-spinning (MAS) nuclear magnetic resonance (NMR), and direct excitation single-pulse 31P MAS NMR analyses suggested the grafting reaction of phosphate and carbamylate groups onto the hydroxyl groups of Kraft lignin. Scanning electron microscopy with energy dispersive X-ray spectroscopy indicated that the condensed Kraft lignin filled the lumen as well as partially penetrating the wood cell wall. The modified Kraft lignin imparted fire-retardancy and increased char residue to the wood at elevated temperature, as confirmed by limiting oxygen index, microscale combustion calorimetry, and thermogravimetric analysis. The modified wood exhibited superior resistance against mold and decay fungi attack under laboratory conditions. The modified wood had a similar modulus of elasticity to the unmodified wood, while experiencing a reduction in the modulus of rupture.