Research Articles

Pinus pinaster Aiton is the pine with the largest natural area of distribution in Spain and the species that sustains the country’s resin industry, with an annual average production of 3.2 to 3.5 kg per tree. After trees have been tapped, their wood has a high resin content and is of little use because of machining difficulties. For the first time, resinous wood of this species was characterized to compare its physico-mechanical properties with those of non-resinous wood. Significant differences were found in all the properties studied except modulus of elasticity. The resin produced by tapping decreased swelling, probably by reducing accessibility to the –OH groups and decreasing the available spaces during the capillary condensation phase. Similarly, tapping caused an increase in wood density and therefore in hardness, at the same time improving the mechanical properties.

The effects of wear on the performance of sanding belts were determined for European beech (Fagus sylvatica L.) and English oak (Quercus robur). These measurements are presented as a function of the defined sanding time of 480 min on a manual sanding belt machine. Sanding belt pressure on the piece surface (6600, 10400, 14700, and 18600 Pa), sanding direction (cutting speed vector with reference to wood fibers equal to 0°, 60° and 90°), wood hydrothermal treatment, and sanding belts from various manufacturers were the variables. The sanding belt wear was monitored by means of specific wood removal rate (g/cm2.min) in 20-min intervals by the means of reference samples with size of 50 x 50 x 50 mm, which were sanded for 1 min. The resulting curves for the sanding belts, as well as the statistical models of the wood removal rate, decreased as a function of the sanding time, described by the function y = a + b.e–ct. This work also describes the impact of wood species, optimum pressure, and grinding time on the characteristics to abrasion.

The effect of biochar addition and turning frequency was examined relative to biochar-chicken manure co-composting and its associated methane (CH4) and carbon dioxide (CO2) emissions. The results demonstrated that biochar addition was more effective in accelerating the composting process, which was indicated by a 5.2% increase in peak pile temperature and a 148% increase in peak CO2 emission with 20% biochar amended-compost, compared with the control that had no biochar. The compost pH increased and moisture content decreased significantly over the whole course of composting with the biochar amendment. The addition of 20% biochar also resulted in a 54.9% decrease in peak CH4 emission compared with the control. More frequent turning (daily vs. every 3 or 7 days) accelerated the composting process and reduced the CH4 emission.

Thermal modification of spruce wood (Picea abies L.) was conducted at three different temperatures (160, 200, and 240 °C) and treatment times (1, 3, and 5 h). The cyclic sorption experiments were performed for relative humidity changes of 30 to 85%. The equilibrium moisture content of the thermally modified wood was reduced up to 50% after treatment at 240 °C for 5 h. The sorption isotherms were described with the Guggenheim, Anderson, and De Boer (GAB) model. Cyclic sorption increased the monolayer capacity. Thus, the monolayer sorption was increased, while the multilayer sorption was limited. The dependence of the mass loss, hysteresis loop, and the maximum difference of equilibrium moisture content on the modification temperature and duration was modeled by response surface methodology. There was a very strong correlation between the modification temperature and mass loss, while the relationship between treatment time and mass loss was insignificant. The correlations between the modification parameters and the descriptors of sorption hysteresis were stronger after cyclic sorption. The sorption hysteresis decreased after cyclic sorption. This result was mainly caused by the increase of the monomolecular sorption for the adsorption processes.

This paper describes preparation of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) mediated oxidized cellulose nanofibers (TOCNs) from corn husk. The process adopted for this work included alkaline treatment, TEMPO/NaBr/NaClO-mediated oxidation, and homogenization. The morphological investigation of TOCNs was performed using atomic force microscopy (AFM) and transmission electron microscopy (TEM). The chemical composition and structure of the material obtained after each stage of the treatments was characterized through Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis. The thermal stability of the samples was investigated by thermogravimetric analysis (TGA). The obtained TOCNs possessed a narrow width, ranging from 8 to 10 nm, and a high aspect ratio (> 300). The crystallinity type of TOCNs was found to be cellulose-Iβ. Compared with the original fibers, the crystallinity of TOCNs gradually increased because of the removal of hemicellulose and lignin, while the thermal stability decreased.

The alkyl-alkoxysilane (AAS) pre-impregnation method and thermal modification were combined to improve the water-related properties of southern yellow pine (Pinus spp.) sapwood. Four types of AAS with varied alkyl chain lengths, including butyltrimethoxysilane (BTMOS), octyltrimethoxysilane (OTMOS), dodecyltrimethoxysilane (DTMOS), and cetyltrimethoxysilane (CTMOS), were used to pre-impregnate wood samples at a concentration of 5% or 15% mass fraction, and the subsequent thermal modification was processed at either 180 °C or 200 °C. The water absorption, dimensional stability, equilibrium moisture content (EMC), mechanical properties (modulus of rupture (MOR), and modulus of elasticity (MOE)), and mold resistance of the treated wood were evaluated. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) were used to reveal the mechanism of the combined treatments in improving the properties of wood. Compared with thermal modification alone, the AAS combined treatment improved the water repellency, mechanical properties, and mold resistance of the modified wood. The study also identified the penetration of AAS into the wood cell wall and its reaction with the chemical components of the cell wall.

Co-polymer systems of methylene diphenyl diisocyanate (MDI) and phenol-formaldehyde (PF) resins with different molecular weights were characterized by infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). The FTIR and TGA coupled with differential thermogravimetric (DTG) results showed that higher molecular weight of PF resins not only promoted the reaction of isocyanate and PF co-polymer system, but also resulted in a better thermal property of prepared co-polymers. The XRD results revealed that higher molecular weight led to a higher proportion of ordered or crosslinking structures in the hybrid resin system. The relationship between the thermal resistance, mechanical properties and the molecular weights of phenolic resins needs further study.

The use of large cross-section timber for structural purposes has increased in Spain, and knowledge of its properties is strategically necessary. The Spanish visual strength-grading standard UNE 56544 (2011) efficiency applied to large cross-section structural timber was analyzed using a sample of 363 specimens of radiata pine (Pinus radiata D. Don.) from the Basque Country and Catalonia, Spain. Different sizes were tested (80 × 120 × 2400 mm3, 150 × 250 × 5600 mm3, 150 × 250 × 4300 mm3, and 200 × 250 × 5000 mm3). Bending strength, modulus of elasticity, and density were obtained, and characteristic values were determined in order to assign strength class according to European standard EN 338 (2010). Knots and twists were the most relevant singularities for visual strength grading. It was concluded that large cross-section Spanish radiata pine timber was suitable for structures, and it was assigned to the C20 strength class.

Pinus pinaster wood was pulped in ethanol/water medium catalyzed with sulfuric acid, and lignin was recovered from the liquid phase by precipitation upon water addition. Lignin samples were characterized for composition and thermal properties. Lignin samples were reacted with selected esterification agents (butyric, isobutyric, or crotonic anhydrides) under experimental conditions leading to extensive conversion of the available hydroxyl groups, and the esterified lignins were assessed for composition and thermal properties. Samples made up of crude polylactic acid or its blends with lignins (raw or esterified) were assayed for mechanical properties. The blends of polylactic acid with lignin modified with butyric anhydride presented higher Young’s modulus and elongation at break than neat polylactic acid.

Cationic rosin has many uses in papermaking; however, its performance as an internal sizing agent differs depending on the circumstance, especially in the recycling of pulps. In this study, a comprehensive laboratory approach was used to investigate the process variables affecting the cationic rosin application in the paper recycling process. In this respect, four levels of alum (0.5, 1.0, 1.5, and 2.0%) and four levels of cationic rosin (0.5, 1.0, 1.5, and 2.0%) were considered to find the best alum/cationic rosin combination in acidic conditions (pH 5). After considering all aspects of the paper, such as the mechanical properties (tensile, burst, and tear indices), wet resistance (Cobb test and dynamic contact angle test), and chemical usage (economically and environmentally-friendly procedures), the 1.0% alum and 0.5% cationic rosin levels were selected for optimum performance. This research also showed that the combined effect of alum with cationic rosin was favorable. Moreover, the sequence of alum and cationic rosin addition, which is a challenge in paper mills, also should be considered. The results indicated that the addition of cationic rosin after alum obtained the best mechanical and wet resistance results. In addition, the results showed that both acidic and neutral pH were acceptable in this sizing process.