Lignin is one of the wood and plant cell wall components that is available in large quantities in nature. Its polyphenolic chemical structure has been of interest for valorization and industrial application studies. Lignin can be obtained from wood by various delignification chemical processes, which give it a structure and specific properties that will depend on the plant species. Due to the versatility and chemical diversity of lignin, the chemical industry has focused on its use as a viable alternative of renewable raw material for the synthesis of new and sustainable biomaterials. However, its structure is complex and difficult to characterize, presenting some obstacles to be integrated into mixtures for the development of polymers, fibers, and other materials. The objective of this review is to present a background of the structure, biosynthesis, and the main mechanisms of lignin recovery from chemical processes (sulfite and kraft) and sulfur-free processes (organosolv) and describe the different forms of integration of this biopolymer in the synthesis of sustainable materials. Among these applications are phenolic adhesive resins, formaldehyde-free resins, epoxy resins, polyurethane foams, carbon fibers, hydrogels, and 3D printed composites.

Low-density polyethylene composites containing different sizes of calcium oxide (CaO) nanoparticles were obtained by melt mixing. The CaO nanoparticles were synthesized by either the sol-gel or sonication methods, obtaining two different sizes: ca. 55 nm and 25 nm. These nanoparticles were used either as-synthesized or were modified organically on the surface with oleic acid (Mod-CaO), at concentrations of 3, 5, and 10 wt% in the polymer. The Mod-CaO nanoparticles of 25 nm can act as nucleating agents, increasing the polymer’s crystallinity. The Young’s Modulus increased with the Mod-CaO nanoparticles, rendering higher reinforcement effects with an increase as high as 36%. The reduction in Escherichia coli bacteria in the nanocomposites increased with the amount of CaO nanoparticles, the size reduction, and the surface modification. The highest antimicrobial behavior was found in the composites with a Mod-CaO of 25 nm, presenting a reduction of 99.99%. This strong antimicrobial effect can be associated with the release of the Ca²⁺ from the composites, as studied for the composite with 10 wt% nanoparticles. The ion release was dependent on the size of the nanoparticles and their surface modification. These findings show that CaO nanoparticles are an excellent alternative as an antimicrobial filler in polymer nanocomposites to be applied for food packaging or medical devices.

Wood chips of Pinus radiata softwood were biotreated with the brown rot fungus (BRF) Gloeophyllum trabeum for periods from 4 and 12 weeks. Biodegradation by BRF leads to an increase in cellulose depolymerization with increasing incubation time. As a result, the intrinsic viscosity of holocellulose decreased from 1,487 cm³/g in control samples to 783 and 600 cm³/g in 4- and 12-week decayed wood chips, respectively. Wood weight and glucan losses varied from 6 to 14% and 9 to 21%, respectively. Undecayed and 4-week decayed wood chips were delignified by alkaline (NaOH solution) or organosolv (ethanol/water) processes to produced cellulosic pulps. For both process, pulp yield was 5–10% lower for decayed samples than for control pulps. However, organosolv bio-pulps presented low residual lignin amount and high glucan retention. Chemical pulps and milled wood from undecayed and 4-week decayed wood chips were pre-saccharified with cellulases for 24 h at 50°C followed by simultaneous saccharification and fermentation (SSF) with the yeast Saccharomyces cerevisiae IR2-9a at 40°C for 96 h for bioethanol production. Considering glucan losses during wood decay and conversion yields from chemical pulping and SSF processes, no gains in ethanol production were obtained from the combination of BRF with alkaline delignification; however, the combination of BRF and organosolv processes resulted in a calculated production of 210 mL ethanol/kg wood or 72% of the maximum theoretically possible from that pretreatment, which was the best result obtained in the present study.

Hemicelluloses from Pinus radiata wood chips were extracted using different conditions of temperature, time and initial pH of water (120 to 170°C, 30 to 120 min and pH 2 to 12, respectively). Results showed that hemicelluloses represented 26% of wood dry weight and, from this amount, hexoses are responsible for 64% of its composition. The analysis of extraction results showed that pH has a low effect in disassembling hemicelluloses from wood, and that time and temperature of reaction were the most important parameters. Maximal amount of hemicellulose extracted in the most severe conditions tested was between 12-16% (on wood basis). In these conditions approximately 40-50% of the hemicellulose in wood was solubilized. As observed by SEC analysis, the recovered hemicellulosic fractions were in the form of low molar mass oligomers with Mw varying from 3720 to 54300 g/mol. The FT-IR spectra show peak multiplicity between 1120 and 1000 cm-1 that is a typical characteristic of carbohydrates and only alkaline-extracted hemicelluloses showed the presence of lignin with a characteristic peak at 1509 cm-1.

As galactoglucomananas são as principais frações de hemiceluloses presentes nas madeiras moles e contêm, principalmente, as hexoses galactose, glicose e manose. O isolamento eficiente e seletivo dessas hemiceluloses é um obstáculo crítico a superar para sua utilização. Os objetivos deste trabalho foram extrair e caracterizar soluções aquosas ácidas e neutras de hemiceluloses de cavacos de madeira de Pinus radiata, bem como avaliar sua viabilidade para a produção de bioetanol. As hemiceluloses em P. radiata representam 26 g/100 g de madeira (base seca), e as hexoses são responsáveis por aproximadamente 64% dessa quantidade. De acordo com as diferentes condições de extração, cerca de 50% da fração hemicelulósica foi solubilizada e recuperada depois de uma precipitação com etanol. As frações recuperadas de hemiceluloses estavam na forma de oligômeros com peso molecular médio (Mw) variando entre 4x10³ e 4x10(5) g/mol. Os oligômeros hemicelulósicos foram hidrolisados com ácido sulfúrico diluído e os hidrolisados concentrados até aproximadamente 70 g/L hexosas e fermentados pela levedura Saccharomyces cerevisiae. Os resultados de fermentação indicaram que os açúcares obtidos dos extratos ácidos e neutros foram fermentados com rendimentos máximos de etanol de 63% e 54% (22 g/L e 19 g/L), respectivamente. A conversão de hemiceluloses da madeira em etanol é viável, porém seu baixo rendimento faz que o processo não seja economicamente atrativo, razão por que melhorias no processo ou usos alternativos das hemiceluloses devem ser avaliados.