No abstract

Plantation poplar (Populus ussuriensis) wood was esterified using acetic anhydride without catalysts to improve its dimensional stability. The effects of acetylation temperature (100 °C, 120 °C, and 140 °C) on the dimensional stability, mechanical properties, microstructure, and functional groups of the resulting acetylated wood were systematically investigated. Results showed that the wood acetylated at 100 °C and 120 °C had an improved dimensional stability and comparable mechanical properties to those of the control wood. Wood acetylated at 140 °C had an improved dimensional stability and decreased mechanical properties as compared to those of the control wood. Scanning electron microscopic (SEM) analysis showed that the wood acetylated at 140 °C had obviously different microstructures than the control wood and the wood acetylated at 100 °C and 120 °C. The changes of functional groups in the acetylated wood were revealed by Fourier transform infrared spectroscopy (FTIR). The -OH groups of cellulose, hemicellulose, and lignin all were shown to participate in the acetylation reaction.

Rubber wood was modified with both a combination of silica sol and glyoxal urea (S-GU), and a combination of silica sol and glyoxal melamine urea (S-GMU). The physico-mechanical properties were measured. Thermal properties, chemical molecular structure, and cellular morphology were analyzed via thermogravimetry (TG), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The weight percent gain (WPG) increased as the concentration of the impregnated aqueous solutions increased. The S-GMU treated wood exhibited a greater WPG than the S-GU treated wood at the same concentration. Anti-swelling efficiency (ASE), modulus of elasticity (MOE), and modulus of rupture (MOR) of treated wood increased as the WPG increased. The highest ASE value was 42.0%, for the S-20%GMU treated wood, which was higher than the S-20%GU treated wood. The MOR of the S-20%GMU treated wood was improved by 25%. Thermal analyses showed the thermostability of S-GMU treated wood increased. FTIR results indicated the presence of C-N and Si-O-Si bonds in the S-GMU treated wood, and the lignin and carbohydrates degraded to a certain extent. SEM imaging showed that the S-GMU was deposited in the cell lumen and cell wall. Therefore, this study produced evidence of an improvement in the physico-mechanical and thermal properties of S-GMU treated wood.

To investigate the changes in the pore structure of earlywood and latewood (EW and LW) in larch during the heat treatment process, this study applied nitrogen adsorption and mercury intrusion porosimetry (MIP) to measure wood pore characteristics. Wood samples were heat treated within a vacuum atmosphere at temperatures between 180 and 220 °C for 6 h. Analysis conducted on nitrogen adsorption isotherms indicated that the micropores and mesopores in the cell walls were present in both untreated and heat-treated EW and LW, and that the mesopores appeared as slit-shaped pores. More pores were detected in EW compared to LW, and these primarily absorbed in the range of 1.5–4 nm. Compared with the untreated wood, the total pore volume of treated wood decreased with increasing temperatures, with decreased pore volumes at 220 °C of 63 and 42% for EW and LW, respectively. The MIP results showed a greater porosity of EW compared to LW. Compared with the untreated wood, the porosity of heat-treated EW and LW first increased with increasing temperature, and then decreased at 220 °C. For treatment temperatures lower than 200 °C, heat treatment increased the proportion of macropores with pore sizes in the ranges of 100–1000 nm and 10,000–40,000 nm.