Volume 10 Issue 4

In this work, lignin polyols were prepared from the liquefaction of kraft lignin and from the direct liquefaction of Elaeis guineensis lignocellulosic waste. The liquefaction reaction was performed with polyhydric alcohols using sulfuric acid as catalyst at 160 °C. The physical and chemical characterizations of lignin and lignin polyols were conducted by elemental analysis, Fourier transform-infrared spectroscopy, 1H and 13C nuclear magnetic resonance (NMR) spectroscopy, molecular weight distribution, and thermogravimetric analysis (TGA). Quantitative 13C NMR showed that all aliphatic hydroxyl group values of polyols noticeably increased with the use of the two methods compared to kraft lignin. The average molecular weight analysis of the liquefied product showed that it exhibited high molecular weight compared to kraft lignin. Both structural and thermal characteristics suggest that lignin polyols would be a good substitute for kraft lignin in the synthesis of polymeric compounds such as environmentally friendly resins or wood adhesives, as it presents higher amounts of activated free ring positions, higher molecular weight, and high thermal stability.

Eichhornia crassipes (water hyacinth) is an invasive weed that causes serious issues for rivers, lakes, and other reservoirs around the world, although it can be an excellent source for bioactive compounds such as phytosterols and some steroids found in many plants. In this study, water hyacinth samples from both Durango and Distrito Federal in Mexico were collected. Ascendant extracts (cyclohexane, hexane, acetone, and methanol) from their leaves, stems, and roots were analyzed. Using boron trifluoride (~10% [~1.3 M] in 1-butanol), all extracts were derivatized. Twenty-four derivatized samples were analyzed using a gas chromatography-mass spectrometry (GC/MS) method. Twenty carboxylic acids were found, as well as squalene, which was found in nine extract samples: four cyclohexane extracts, one hexane extract, three acetone extracts, and two methanol extracts. A compound not reported before, b-stigmasterol, was identified on three hexane extracts, an acetone extract, and a methalonic extract. Spirostane in acetone root extract and cholestane in cyclohexane stem-leaf extract were also identified.

The effects of pH and sulfonated lignin (SL) on the saccharification of enzymatic hydrolysis were investigated using acid bisulfite (AS)- and green liquor (GL)-pretreated poplar as substrates. The enzymatic sugar conversions of AS- and GL-pretreated poplar could reach high levels at pH 4.8. The sugar conversions of both AS- and GL-pretreated poplar solids increased when hydrophilic SL was used as an additive in the enzymatic hydrolysis. With SL addition, the optimal pH of AS-pretreated poplar moved to 5.1–5.7, while that of GL-pretreated poplar showed no significant difference. The sugar conversions of AS- and GL-pretreated poplar went up and then leveled off with SL charges from 0.05 to 0.3 g/g-substrate. The highest total sugar conversions increased from 76.4% and 86.9% (pH 4.8, without SL) to 83.5% (pH 5.4, SL 0.3 g/g-substrate) and 90.9% (pH 5.0, SL 0.2 g/g-substrate) for AS- and GL-pretreated poplar, respectively.

Unbleached kraft bamboo pulp was pretreated by a xylanase and laccase (X/L) treatment, as well as a joint treatment of X/L and alkali, prior to element chlorine free (ECF) bleaching. In comparison with the control test, the joint treatment of X/L and alkali (X/L+0.1%) had more potential to reduce absorbable organic halide (AOX) levels (29.79%) and COD content (21.55%), in addition to improving bleached pulp properties (56.88% decrease in kappa number and 8.94 %ISO increased in brightness). Moreover, the treatment of X/L+0.1% removed more lignin and HexA than X/L treatment. The analysis of XPS indicated that the X/L treatment could noticeably remove the surface lignin of pulp, but the joint treatments of X/L and alkali could promote the production of superficial lignin. FTIR results showed that pretreatments only reduced part of the lignin and carbohydrate contents, but did not change their structures. The joint pretreatment of enzymes and diluted alkali (X/L+0.1%) had more appealing advantages to produce bleached kraft bamboo pulp.

Biocomposites based on poly(L-lactic acid) (PLA) and non-woven jute fabrics (NWJF) were fabricated by sandwiching non-woven jute mat between PLA sheets. First, composites were fabricated with various weight proportions of jute fabric (5, 10, 20, and 30 wt.%) with the PLA matrix, and the effect of fabric loading on their mechanical properties was investigated. Higher mechanical properties were found at 10 wt.% fabric-loaded composite. The results show that the tensile, flexural, and impact strengths were increased by 61.7, 52.3, and 47.2%, respectively, as compared with neat PLA. In the second part, the jute fabrics were chemically treated with NaOH, NaClO2, acrylonitrile, acetic anhydride, KMnO4, diphenylmethane diisocyanate, and benzoyl chloride. The effect of chemical treatment on the mechanical and water absorption properties of NWJF/PLA biocomposites was studied. The mechanical properties of these biocomposites were found to be higher than those of untreated biocomposites. Among all the treatments, the combined alkali-benzoylated-treated fabric composite showed higher mechanical properties. The water absorption properties of these composites were found to be remarkably lower than those of untreated fibers. The interfacial adhesion between the fiber and the matrix was shown to increase with surface modification as revealed by SEM analysis.

A photocatalytic fiber was prepared by modifying the surface of jute fiber with a Bi2O3/TiO2 composite. Maleic acid was used as an organic linker, and the coating process was conducted with heat-treatment at 240 °C. At first, the Bi2O3/TiO2 composite was synthesized by incorporating TiO2 nanoparticles onto a Bi2O3 phase. Subsequently, the photocatalytic fiber was prepared by incorporating the Bi2O3/TiO2 composite onto the surface of the fiber. The Bi2O3/TiO2 composite-modified fiber was characterized by field-emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and UV-visible spectroscopy. The synthesized composite exhibited notably high photocatalytic activity under visible light irradiation of λ up to 420 nm, whereby it could decompose organic pollutants in the aqueous and gaseous phases. Because of increasing environmental concerns, this photocatalytic system could be an important candidate for decomposing organic pollutants.

Manufacturing glued laminated timber (glulam) can help overcome the limited availability of large-sized timber, and the use of bio-adhesives may resolve environmental problems associated with synthetic adhesives containing high formaldehyde contents. Tannin adhesive is a bio-adhesive that can be used as alternative glue in the manufacture of glulam. The purpose of this study was to determine the physical and mechanical properties of glulam made with mahogany (Swietenia sp.) tannin adhesive and wood from three fast-growing species, namely pine (Pinus merkusii), jabon (Anthocephalus cadamba), and sengon (Falcataria moluccana). Glulam (3 cm × 6 cm × 120 cm in thickness, width, and length, respectively) was manufactured with three layers of lamina. The physical and mechanical properties of the glulams were tested based on relevant standards. The results showed that pine glulam fulfilled the standard for the modulus of rupture and modulus of elasticity, while sengon glulam met the standard for shear strength. In the delamination test, sengon glulam was resistant to immersion in cold water and hot water. All glulams had low formaldehyde emission levels and therefore fulfilled the standard requirements. The results showed that the tannin adhesive from mahogany bark was equal in quality to methylene diphenyl di-isocyanate for glulam manufacturing.

In order to improve the whiteness of fly ash, the particles were coated by in-situ precipitation of calcium carbonate. After different mass ratios of calcium oxide to fly ash were mixed into water, a certain amount of carbon dioxide was bubbled into the mixture to form a precipitated calcium carbonate deposit on the surface of fly ash. With the help of scanning electron microscopy (SEM), the process and the coating mechanism of the unmodified and modified fly ash were studied. The results showed that when a 1:1 mass ratio of calcium oxide to fly ash was implemented, the whiteness of fly ash was increased from 30.3 (the original fly ash) to 74.0 (the modified fly ash). After appropriately controlling for the rate of carbon dioxide, the whiteness was improved to meet the standard for filler in the papermaking industry, and also great advantages in paper physical strength were demonstrated.

Extraction of hemicelluloses prior to pulping and conversion of the extracted hemicelluloses to other bioproducts could provide additional revenue to traditional pulp and paper industries. The effect of hemicelluloses pre-extraction with a hydrothermal (HT) process on Pinus radiata chemimechanical pulp (CMP) properties was investigated in this study. The HT extraction resulted in a release of 7% to 58% of the initial amount of hemicelluloses from the wood. The extraction yield increased with temperature and extraction time. This hemicellulosic fraction was in the form of low molar mass oligomers with molecular weights varying from 1.5 to 100 kDa. Compared with the control (unextracted) CMP pulp, the HT pre-extraction significantly reduced the refining energy to obtain a given fibrillation degree (freeness). The pulp yield with the HT/CMP process was in the range of 56% to 75%. Fiber properties of the pulps from pre-extracted wood, such as fiber length, were reduced, while increases in fiber width, fines content, fiber coarseness, and kink index were observed in comparison with the control pulps. The strength properties of CMP pulps decreased with increasing amounts of hemicellulose removal during the stage prior to pulping.

Three types of reinforcement materials, a carbon fiber-reinforced polymer (CFRP) sheet, a glass fiber-reinforced polymer (GFRP) mesh, and a composite of the CFRP sheet and GFRP mesh, were used to reinforce poplar laminated veneer lumber (LVL), and the multi-step hot-pressing method was also applied. The mechanical properties, i.e., modulus of rupture (MOR), modulus of elasticity (MOE), and horizontal shear strength (HSS), of the reinforced LVL were investigated, as well as the effects of lay-up location of the CFRP sheet/GFRP mesh composite. The results indicated that applying the multi-step hot-pressing method and incorporating the CFRP sheet, GFRP mesh, and the CFRP sheet/GFRP mesh composite noticeably improved the MOR and MOE under horizontal and vertical loadings. Only the multi-step hot-pressing method was able to greatly improve the HSS of reinforced LVL under both loading modes. The improved effect of the three kinds of reinforcing materials on the mechanical properties was ordered as follows: CFRP sheet/GFRP mesh composite > CFRP sheet > GFRP mesh. Locating the CFRP sheet/GFRP mesh composite closer to the surface veneer layer yielded the best mechanical properties for the reinforced poplar LVL.