An approach based on the recycling of waste plywood as a recovered wood resource for the particleboard industry is described. It is demonstrated that post-industrial urea- (UF) and phenol-formaldehyde (PF) bonded plywood can be effectively shredded to the form of the recovered particles that can be a valuable material in particleboard manufacturing. The effects of shredding conditions and binder type on the recovered particles characteristics and the mechanical properties of the particleboards were analyzed. It is shown that the substitution of 20–100% of virgin particles with the recovered material is possible without affecting the performance of the particleboard.
Black poplar (Populus nigra L.) was thermally modified in nitrogen atmosphere. The effects of the modification process on poplar wood were evaluated for temperatures: 160 °C, 190 °C, and 220 °C applied for 2 h; and 160 °C and 190 °C for 6 h. The percentual impact of temperature and time of modification on the properties of modified wood was analysed. The study permitted the identification correlations between the chemical composition and selected physical properties of thermally modified poplar wood. The dimensional stability of poplar wood was improved after thermal modification in nitrogen. The higher the temperature of modification, the lower the equilibrium moisture content (EMC) of black poplar. At the temperature of 220 °C, EMC was two times lower than the EMC of non-modified black poplar. It is also possible to reduce the dimensional changes of wood two-fold (at the modification temperature of 220 °C), both in radial and tangential directions, independently of the acclimatization conditions (from 34% to 98% relative humidity, RH). Similar correlations have been found for wood that has been soaked in water. Higher modification temperatures and longer processing times contributed to a lower swelling anisotropy (SA).
This study examined the influence of temperature and time of treatment on the density profile and hardness of surface-densified birch wood (Betula pendula Roth). An analysis of the wood density profile was conducted on the basis of the following parameters: thickness, maximum density, and the distance between the maximum density and the wood surface. Depending on the technological parameters’ values, the degree of compression of the wood was 13% to 22%, and its maximum density was 808 kg/m3 to 994 kg/m3. As a result of the modification of birch wood at a temperature of 100 °C and 125 °C, the wood was densified on one side. As the temperature of the thermo-mechanical treatment was raised from 150 °C to 200 °C, the wood became densified on both sides. The maximum density of the wood increased gradually with the increase of the temperature of the press plate. The longer the time of thermo-mechanical treatment, the more distant the maximum density area was from the wood surface. Depending on the temperature and the time of treatment, the hardness of the surface-densified birch wood was 1.4 to 2.2 times greater than the hardness of non-densified wood.
European oak wood (W) was thermo-mechanically modified (TM) via densifying at 100 and 150°C and the surface properties of the TMW were investigated. The contact angle (CA) of the wood with the reference liquids water and diiodomethane was determined using the sessile drop method. The surface free energy of the TMW on tangential sections within the first 60 s after applying a drop was analyzed. The roughness parameters Ra and Rz parallel (‖) and perpendicular (⊥) to the grain were investigated. The wettability analysis showed that densified wood had a higher CA and lower work of adhesion and surface free energy than non-densified wood. An X-ray photoelectron spectroscopy [XPS or electron spectroscopy for chemical analysis (ESCA)] analysis showed that the oxygen to carbon atoms ratio (O/C ratio) of densified wood surface was lower than that of non-densified wood. The carbon C1-C2 atoms ratio (C1/C2 ratio) increased with increasing TM temperature. The results were interpreted as being that extractives migrate to the surface and amorphous and glassy polymers, i.e. lignin and hemicelluloses, in wood are rearranged. Increasing densification temperature makes TMW surfaces more hydrophobic.