Effect of thermal modification on the surface quality of a coating applied to wood via the electrostatic spray deposition technique

The surface properties of thermally modified ash wood with a powder coating were investigated, and the results were compared to the unmodified wood. The wood specimens were sanded with 80 grit sandpaper and then pre-heated at 80 °C for 5 min in an infrared oven. The surface of the unmodified and the modified wood specimens were coated with an epoxy/polyester (1 to 1 ratio) hybrid coating using an electrostatic corona spray gun at the pilot plant established in the laboratory. The coatings on the wood specimens were cured at different curing conditions in an infrared oven, i.e., 120 °C/15 min, 140 °C/10 min, and 160 °C/10 min. The results showed that the thermal modification (TM) of the wood caused a slight decrease in the mechanical performance of the surface system (wood substrate and coating film). For example, the scratch and abrasion resistance of the unmodified specimens at the curing temperature of 120 °C were 3.33 N and 135 revolutions but were 3.12 N and 120 revolutions after the TM. However, the average surface roughness (1.26 mu) and contact angle (60.8°) of the distilled water on the cured coatings on the modified wood were lower than those on the unmodified wood (1.86 mu and 80.8°, respectively).

Influence of Citric Acid on the Bond Strength of Beech Wood

In this study, beech wood (Fagus silvatica L.) has been chemically modified with citric acid (Acidum citricum) and sodium hypophosphate (SHP) as the catalyst and gradually thermo-condensed in the dryer. Afterwards, wetting angle, surface energy, and shear strength of glued joints of modified and unmodified wood were determined. Testing of the bond strength according to standard EN 204 and comparison between modified and unmodified samples were executed. The adhesive used for bonding samples was polyvinyl acetate (PVAC), commonly used for gluing solid wood panels. Testing material was divided into three groups (dry, wet, and wet conditioned samples), within which statistical analysis was performed, and the significance of the differences between the modified and unmodified samples was determined. Surface energy is correlated with the bond strength, indicating that modification with citric acid negatively affects the adhesive properties of beech wood. A reduction in the bond strength of modified wood glued with PVAC glue compared to unmodified wood was determined. All the results indicate that the modified samples do not meet the minimum requirements for EN 204 bonded with PVAC glue. Therefore, it will be necessary to conduct further studies using other types of adhesives to investigate whether modified wood might be suitable for gluing.

Comparative Adhesive Bonding of Wood Chemically Modified with Either Acetic Anhydride or Butylene Oxide

Determining adhesive bond performance for chemically modified wood is important not only for its commercial utility but also for understanding wood bond durability. Bulking modifications occupy space inside the cell wall, limiting the space available for water. We used two bulking modifications on yellow poplar (Liriodendron tulipifera L.): acetylation (Ac), which bulks and converts a wood hydroxyl group to an ester, while butylene oxide (BO) also bulks the wood but preserves a hydroxyl group. Both result in lower water uptake; however, the loss of the hydroxyl group with Ac reduces the wood’s ability to form hydrogen and other polar bonds with the adhesives. On the other hand, the BO reaction replaces a hydroxyl group with another one along a hydrocarbon chain; thus, this product may not be harder to bond than the unmodified wood. We investigated how these chemical modifications of wood affect bond performance with four adhesives: resorcinol-formaldehyde (RF), melamine-formaldehyde (MF), emulsion polymer isocyanate (EPI), and epoxy. The ASTM D 905 bond shear strength for both dry and wet samples showed that the BO results were quite similar to the unmodified wood, but the MF and EPI performed poorly on Ac-modified wood, in contrast to the results with RF and epoxy.

Moisture-dependency of the fracture energy of wood: a comparison of unmodified and acetylated Scots pine and birch

The moisture-dependency of the fracture energy for unmodified and acetylated Scots pine (Pinus sylvestris L.) and birch (Betula pendula Roth) has been investigated. Specimens were conditioned at relative humidity levels of 20, 75, and 97%, as well as dry and water-saturated. At moisture contents below 15%, the fracture energy increased with increasing moisture content for both unmodified and acetylated wood, while it decreased for untreated wood at higher moisture contents. A significant difference in moisture-dependency was found, indicating higher fracture energy for unmodified wood compared to acetylated wood at similar moisture contents. Additionally, to assess the impact of the increased brittleness for structural applications, the fracture energy was compared at equal relative humidity levels. The largest difference was seen at 75% relative humidity with approximately 50% lower fracture energy for acetylated wood. No significant differences were found for water-saturated samples. The moisture-dependency of the fracture energy, combined with the reduced hygroscopicity of acetylated wood, is suggested to be one, but not the only, contributing factor to the lower fracture energy of acetylated wood compared to unmodified wood at equal humidity levels. These observations have importance for structural design since design codes often assess material parameters based on ambient humidity.

Properties of Pinus modified with silicon–titanium binary oxides

Modification of Pinus yunnanensis using SiO2–TiO2 was carried out via the sol–gel method. The aim was to improve the hydrophobicity, aging resistance, and photocatalysis of the wood surface via the formation of new chemical bonds with penetrated SiO2 and TiO2. The air-dried P. yunnanensis wood underwent penetration, gelation, aging, and drying. The wood was exposed to high temperatures for modification, and its microstructure, composition, photodegradability, resistance to aging, dimensional stability, and hydrophobicity were then determined. The results indicated that during modification, SiO2–TiO2 gel was generated in the wood, and the content of the gel increased as penetration time was extended. No structural change in the wood was observed. Meanwhile, chemical bonds were formed among SiO2, TiO2, and wood. The contact angle of the modified wood increased noticeably relative to that of unmodified wood. This increase indicated a noticeable increase in the hydrophobicity of the wood surface. The modified wood exhibited high photocatalytic degradation; however, its durability was not evident. The water absorption and thickness swelling of the modified wood markedly increased. After ultraviolet-aging resistance testing, the color change in the surface of the modified wood was noticeably less than that of the unmodified wood.

Suitability and Modification of Different Renewable Materials as Feedstock for Sustainable Flame Retardants

Due to their chemical structure, conventional flame retardants are often toxic, barely biodegradable and consequently neither healthy nor environmentally friendly. Their use is therefore increasingly limited by regulations. For this reason, research on innovative flame retardants based on sustainable materials is the main focus of this work. Wheat starch, wheat protein, xylan and tannin were modified with phosphate salts in molten urea. The functionalization leads to the incorporation of phosphates (up to 48 wt.%) and nitrogen (up to 22 wt.%). The derivatives were applied on wood fibers and tested as flame retardants. The results indicate that these modified biopolymers can provide the same flame-retardant performances as commercial compounds currently used in the wood fiber industry. Besides, the flame retardancy smoldering effects may also be reduced compared to unmodified wood fibers depending on the used biopolymer. These results show that different biopolymers modified in phosphate/urea systems are a serious alternative to conventional flame retardants.

Occupational Exposure to Dust Produced when Milling Thermally Modified Wood

During production, thermally modified wood is processed using the same machining operations as unmodified wood. Machining wood is always accompanied with the creation of dust particles. The smaller they become, the more hazardous they are. Employees are exposed to a greater health hazard when machining thermally modified wood because a considerable amount of fine dust is produced under the same processing conditions than in the case of unmodified wood. The International Agency for Research on Cancer (IARC) states that wood dust causes cancer of the nasal cavity and paranasal sinuses and of the nasopharynx. Wood dust is also associated with toxic effects, irritation of the eyes, nose and throat, dermatitis, and respiratory system effects which include decreased lung capacity, chronic obstructive pulmonary disease, asthma and allergic reactions. In our research, granular composition of particles resulting from the process of longitudinal milling of heat-treated oak and spruce wood under variable conditions (i.e., the temperature of modification of 160, 180, 200 and 220 °C and feed rate of 6, 10 and 15 m.min−1) are presented in the paper. Sieve analysis was used to determine the granular composition of particles. An increase in fine particle fraction when the temperature of modification rises was confirmed by the research. This can be due to the lower strength of thermally modified wood. Moreover, a different effect of the temperature modification on granularity due to the tree species was observed. In the case of oak wood, changes occurred at a temperature of 160 °C and in the case of spruce wood, changes occurred at the temperatures of 200 and 220 °C. At the temperatures of modification of 200 and 220 °C, the dust fraction (i.e., that occurred in the mesh sieves, particles with the size ≤ 0.08 mm) ranged from 2.99% (oak wood, feed rate of 10 m.min−1) to 8.07% (spruce wood, feed rate of 6 m.min−1). Such particles might have a harmful effect on employee health in wood-processing facilities.

The Biological Durability of Thermally- and Chemically-Modified Black Pine and Poplar Wood Against Basidiomycetes and Mold Action

Wood of black pine and poplar species were subjected to thermal modification under variant conditions, while subsequently, a number of the thermally-modified black pine specimens were subjected to surface modification with organosilane solutions, and the biological resistances of the different materials were examined using laboratory agar block tests against the action of basidiomycetes and microfungi. Thermally-modified pine specimens were exposed to the brown rot fungi Coniophora puteana and Oligoporus placenta, whereas poplar wood was exposed to the white rot fungus Trametes versicolor and O. placenta. Regarding the biological durability of thermally-chemically-treated pine wood with organosilanes, it was tested against the action of C. puteana. Additionally, both of the thermally-treated wood species, as well as thermally-chemically-treated pine wood were exposed to a microfungi mixture, so that the wood treatments efficacy would be evaluated through a visual assessment of fungal growth on the specimen’s surface The thermal treatments seem to increase the biological resistance of black pine against C. puteana by 9.65–36.73% compared to unmodified wood. The most significant increase in biological durability among all the thermally-treated wood categories was recorded by O. placenta, with 28.75–68.46% lower mass losses in treated pine specimens and 31.98–64.72% in thermally-treated poplar, respectively, compared to unmodified wood. The resistance of treated poplar against T. versicolor was also found increased (13.25–46.08%), compared to control. Thermal modification affected positively the biological resistance of both species, though it did not manage to protect effectively pine and poplar wood from the microfungi action. The combination of thermal and organosilanes treatment revealed a significant improvement of the durability of pine wood compared to? control (45.68–87.83% lower mass losses against C. puteana), as well as against the microfungi action, with the presence of benzin to have a positive effect on the silanes solutions performance and protective action.

Effects of Moisture on Diffusion in Unmodified Wood Cell Walls: A Phenomenological Polymer Science Approach

Despite the importance of cell wall diffusion to nearly all aspects of wood utilization, diffusion mechanisms and the detailed effects of moisture remain poorly understood. In this perspective, we introduce and employ approaches established in polymer science to develop a phenomenological framework for understanding the effects of moisture on diffusion in unmodified wood cell walls. The premise for applying this polymer-science-based approach to wood is that wood polymers (cellulose, hemicelluloses, and lignin) behave like typical solid polymers. Therefore, the movement of chemicals through wood cell walls is a diffusion process through a solid polymer, which is in contrast to previous assertions that transport of some chemicals occurs via aqueous pathways in the cell wall layers. Diffusion in polymers depends on the interrelations between free volume in the polymer matrix, molecular motions of the polymer, diffusant dimensions, and solubility of the diffusant in the polymer matrix. Because diffusion strongly depends on whether a polymer is in a rigid glassy state or soft rubbery state, it is important to understand glass transitions in the amorphous wood polymers. Through a review and analysis of available literature, we conclude that in wood both lignin and the amorphous polysaccharides very likely have glass transitions. After developing and presenting this polymer-science-based perspective of diffusion through unmodified wood cell walls, suggested directions for future research are discussed. A key consideration is that a large difference between diffusion through wood polymers and typical polymers is the high swelling pressures that can develop in unmodified wood cell walls. This pressure likely arises from the hierarchical structure of wood and should be taken into consideration in the development of predictive models for diffusion in unmodified wood cell walls.

On the Experimental Assessment of the Molecular-Scale Interactions between Wood and Water

Although molecular-scale wood-water interactions needed for moisture-durability can lead to the accelerated development of moisture-durable products, these interactions are often experimentally elusive. In this perspective, the topic’s state of the art understanding will be discussed, excluding computational work. Recent research efforts based on infrared spectroscopy methods have provided new insights in terms of the accessibility of the wood polymers and moisture-induced polymer dynamics. Likewise, neutron scattering and nuclear magnetic relaxometry experiments have shown that bound water can be found within more than one local environment inside the cell wall. However, a majority of the experiments have focused on studying extracted or derived polymers instead of unmodified wood. Thus, in this paper some of the questions that still need to be addressed experimentally will also be highlighted.