Research Articles

A slow pyrolysis of pinewood was investigated in this paper. Through the briquette process, the pinewood sawdust becomes molded biomass. The molded bio-char was produced from molded biomass with different pyrolysis factors, and the bio-char’s heating value, char yield rates, and physicochemical and morphological properties were investigated. Molded bio-char’s characteristics depended principally on pyrolysis factors. At low temperature (400 °C), the char yield rate was positively correlated to the heating rate. But at higher temperatures (500 to 700 °C), the char yield rates decreased as heating rates increased. As pyrolysis temperature increased from 400 to 700 °C, the following increased in molded bio-char: fixed-carbon content, percentage carbon, heating value, ash content, as well as surface areas. And its pore structure, graphite degree, and polymerization degree achieved a higher level. Compared with pulverized bio-char, the molded bio-char had a higher char yield rate, ash content, graphite degree, and structure ordering. The molded bio-char obtained from a low temperature (400 °C) and high heating rate (15 °C/min) can be used as a reducing agent, the molded bio-char from 600 °C is recommend as an activated carbon precursor, and the molded bio-chars from low temperature (400 °C) have a higher efficiency as fuel.

The fuel properties of wood obtained from sugar maple (SM) and yellow birch (YB) of temperate hardwood stands located in the Province of Québec, Canada were studied to see how tree vigor affects the chemical composition and calorific value of the wood. This study focused on the physical and chemical properties of wood with the aim of using the material for the production of solid biofuels. Specific items measured included the wood’s calorific values, and the levels of extractives, ash, and lignin. Changes in chemical composition were found among tree vigor classes. The low vigor trees had higher extractives, ash, and lignin contents than the vigorous trees. Total extractives ranged between 4.88 and 7.32% in SM, and between 3.35 and 5.12% in YB. Klason lignin ranged between 21.46 and 23.53% in SM, and between 18.60 and 21.51% in YB. Ash content ranged between 0.38 and 0.97% in SM, and between 0.26 and 0.47% in YB. The combined effects of higher lignin content that could contribute to a better self-bonding of particles and of higher extractives content that could facilitate the pelletization process makes the low vigor trees more suitable for conversion into solid biofuels. The higher amounts of extractives and lignin present in the low vigor sugar maple and yellow birch trees could also have a positive role in maintaining the high calorific values of this wood despite higher ash content.

Fiber membranes prepared from jute fragments can be valuable, low cost, and renewable. They have broad application prospects in packing bags, geotextiles, filters, and composite reinforcements. Traditionally, chemical adhesives have been used to improve the properties of jute fiber membranes. A series of new laccase, laccase/mediator systems, and multi-enzyme synergisms were attempted. After the laccase treatment of jute fragments, the mechanical properties and surface hydrophobicity of the produced fiber membranes increased because of the cross-coupling of lignins with ether bonds mediated by laccase. The optimum conditions were a buffer pH of 4.5 and an incubation temperature of 60 °C with 0.92 U/mL laccase for 3 h. Laccase/guaiacol and laccase/alkali lignin treatments resulted in remarkable increases in the mechanical properties; in contrast, the laccase/2,2’-azino-bis-(3-ethylthiazoline-6-sulfonate) (ABTS) and laccase/2,6-dimethoxyphenol treatments led to a decrease. The laccase/ guaiacol system was favorable to the surface hydrophobicity of jute fiber membranes. However, the laccase/alkali lignin system had the opposite effect. Xylanase/laccase and cellulase/laccase combined treatments were able to enhance both the mechanical properties and the surface hydrophobicity of jute fiber membranes. Among these, cellulase/laccase treatment performed better; compared to mechanical properties, the surface hydrophobicity of the jute fiber membranes showed only a slight increase after the enzymatic multi-step processes.

The effect of timber length on time-of-flight acoustic longitudinal measurements was investigated on the structural timber of four Spanish species: radiata pine (Pinus radiata D. Don), Scots pine (Pinus sylvestris L.), laricio pine (Pinus nigra Arn.), and maritime pine (Pinus pinaster Ait.). Time-of-flight longitudinal measurements were conducted on 120 specimens of dimensions 90 × 140 mm using three commercially available acoustic instruments (Sylvatest Duo, USLab, and Microsecond Timer). Time-of-flight data were initially obtained from the full-length (4 m) specimens, and then from the specimens cut to 3, 2, and 1 meter in length by successively cutting off 0.5 m from each end. The acoustic longitudinal velocity of the timber specimens of different lengths was also measured using a resonance-based acoustic method. The apparent acoustic longitudinal velocity for all species increased linearly as the timber length decreased from 4 to 1 meter. Acoustic velocity determined from time-of-flight data was significantly higher than the acoustic velocity determined using the resonance method, indicating systematic measurement errors associated with the time-of-flight instruments. Empirical models were developed for the relationships between time-of-flight measurements on timber specimens and timber lengths in the range of 1 to 4 m. Finally, a procedure was proposed to correct the time-of-flight data.

To achieve value-added utilizations of plantation timbers, eucalyptus veneer/high-density polyethylene film composites were prepared, with process-factors (PF) (hot-pressing temperature, HT; hot-pressing duration, HD; hot-pressing pressure, HP; HDPE-film content, HC) and composite-properties (CP) (water-resistant bonding-strength, BS; modulus of rupture, MOR; modulus of elasticity, MOE) investigated. According to thermal analyses, 140 to 180 °C was appropriate for HT. Based on statistical analyses, HD was easier to affect CP, while MOE was easier to be affected by PF. Quantitative relationships between PF and CP were determined by the neural-network (ANN) modeling. In ANN simulation surveys, CP displayed Gaussian distributions (R2 > 0.9) when PF changed in current ranges, with positive correlations between BS and MOR (R2 ≈ 0.5). Combining ANN and the genetic-algorithm, optimal processes (HT, 160 °C; HD, 50 s/mm; HP, 1.3 MPa; HC, 6 layers) were found, and optimal results (BS, 1.30 MPa; MOR, 86.94 MPa; MOE, 8.33 GPa) were comparable to various reported poplar-plywoods. Microscopic images demonstrated that composite interfaces were formed by the mechanical interlocking. The optimal BS attained Chinese standards for water-resistant plywoods, so proposed composites can serve as water-resistant and formaldehyde-free building materials for furniture and interior design.

This study demonstrated the reinforcing potential of kenaf core fiber (KCF) to complement and sustain oil palm fiber supply chain in the production of natural fiber-thermoplastic biocomposites. The lignin-rich KCF was incorporated into cellulose-rich oil palm empty fruit bunch fiber (EFBF)- and oil palm mesocarp fiber (OPMF)-poly(lactic acid) (PLA) composites, aimed at achieving synergism. The hybrid biocomposites developed by melt blending and subsequent compression molding were characterized for possible application as an alternative to medium-density fiberboards. The mechanical properties and dimensional stability of both single fiber- and hybrid fiber-PLA biocomposites were evaluated and compared. The test results showed a synergistic improvement as a consequence of fiber hybridization. Also, the findings suggested the best material performance with the incorporation of 5% KCF into 55% EFBF or OPMF and 40% PLA matrix. The OPMF-KCF-PLA hybrid biocomposites gave better results than the EFBF-KCF-PLA hybrid biocomposites.

The objective of this study was to explore the influence of pyrolysis temperature on the physicochemical properties of biochar synthesized from durian wood (Durio zibethinus) sawdust. Surface morphological features, including the porosity and BET surface area of biochars, provide appropriate dimensions for growing clusters of microorganisms with excellent water retention capacity in soil. Oxygen-containing surface functional groups play a vital role in improving soil fertility by increasing its cation and anion exchange capacities with reduced leaching of nutrients from the soil surface. Biochar was produced via slow pyrolysis of woody biomass (WS) using a fixed bed reactor under an oxygen-free atmosphere at different pyrolysis temperatures (350, 450, and 550 °C). The biochars obtained were characterized using ultimate and proximate analyses, Brunauer-Emmett-Teller (BET) surface area, field-emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The yield of biochar decreased from 66.46 to 24.56%, whereas the BET surface area increased sharply from 2.567 to 220.989 m2/g, when the pyrolysis temperature was increased from 350 to 550 °C. The results highlighted the effect of pyrolysis temperature on the structure of the biochar, which could be advantageous for agricultural industries.

The global production and use of wood fuel pellets has increased significantly in recent years. The raw material and the energy required to dry it are the main production costs. Therefore, it is crucial to minimize energy consumption, production costs, and the environmental impact associated with wood pellets. However, these changes should not negatively affect the quality of the pellets. One way to achieve these goals is to use additives. This work investigates how different types of sugar additives affect both the energy needed by the pellet press and the durability and oxidation of the produced pellets. When sugar was used as an additive, the energy use was practically unaffected. When molasses and SSL were added, a small decrease in energy use was observed (6 to 8%) for admixtures up to 1 wt.%; however, when more molasses was added, the energy use increased. Using these additives increased the bulk density (7 to 15 %) and durability (10 to 20 %) of the pellets. The storage of the pellets also caused a small increase in durability (1 to 3 %). Volatile organic compounds were produced as oxidation peaks within the first two months of storage; thereafter, the peaks tapered off.

To prepare activated carbons with a high porosity and low ash content from pyrolyzed rice husk, the method of KOH or K2CO3 solution leaching after CO2 activation was investigated. The effects of KOH or K2CO3 concentration and leaching time on the yield, ash content, and textural properties of the activated carbon were studied, and the activated carbon prepared under the best conditions was characterized. The results showed that the best leaching time was 1 h for KOH and K2CO3, and the best concentrations were 1.0 and 4.0 M, respectively. The leaching process was greatly beneficial to the development of the pore structure. The specific surface area of the activated carbon prepared under the most favorable conditions was approximately 1100 m2/g, and the iodine values were greater than 1100 mg/g. As a result of the leaching process, the ash content of the sample was notably decreased from 63% to approximately 5%, andthe porosity development was attributed to the reaction of the leaching reagents with silica.

This study focuses on the extraction of nanocrystalline cellulose (NCC) from the dried stalk of Corchorus olitorius,commonly known as jute,using a combination of a microwave-assisted alkaline peroxide pulping process (AHP) and ultrasonication. Dried jute stalk powder was pretreated using sodium hydroxide under microwave irradiation for the removal of lignin. The partially delignified sample was bleached using 30% hydrogen peroxide solution. The resulting crude cellulose was hydrolyzed using ultrasonication in the presence of ionic liquid and sulfuric acid. The effect of hydrolyzing medium on the physicochemical characteristics of the extracted nanocellulose was investigated. The nanocrystalline cellulose (NCC) obtained after combined treatments was rod-like, with diameters of 10 to 15 nm and lengths of 92 to 105 nm. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction analysis (XRD) showed that some breakages of intramolecular hydrogen bonds and glycosidic bonds occurred during the hydrolysis reaction of pretreated biomass. Ultrasonication in the presence of an acid hydrolyzing medium most effectively accelerated these breakages in the long chain cellulose biopolymer, leading to the formation of nanocrystalline cellulose (NCC) with higher crystallinity.