Search Results (36)

Rapeseed stalks (Brassica napus), an abundant agricultural residue, represent a promising non-woody raw material for the pulp and paper industry. This study focuses on the chemical and structural characterization of alkali lignins isolated from black liquors generated by two common delignification methods: Kraft and Soda-Anthraquinone Pulping of rapeseed stalks. The objective is to understand how the chemical environment of each process influences the final structure, fragmentation degree, and reactivity of the isolated lignin. In practice, lignin samples are recovered from black liquors produced under varying conditions (alkali charge, time, and temperature) to achieve defined levels of delignification. Detailed characterization was performed using advanced analytical techniques, including Gel Permeation Chromatography, Solid-State Cross-Polarization/Magic-Angle-Spinning Nuclear Magnetic Resonance, and FT-IR and UV-Vis Spectroscopy. The findings provide essential data on the structural differences, confirming the suitability of the resulting materials for potential high-value applications. Furthermore, the structural similarities and performance indicators suggest that the Soda-AQ process enables successful delignification of rapeseed stalks without the sulfur emission issues associated with the Kraft method, thus validating the former as an environmentally cleaner alternative for non-wood biomass utilization supporting the complete valorization of rapeseed agricultural waste. Full article

The study explores γ-valerolactone (GVL) pulps as a sustainable approach to producing microfibrillated (MFC) and nanofibrillated (NFC) cellulose from sugarcane bagasse, a widely available agro-industrial by-product. Pulp was obtained by acid-catalyzed organosolv delignification with a GVL–water system. MFC was generated through a simple disc refiner, while NFC was produced by TEMPO-mediated oxidation followed by mechanical treatment in a colloidal mill. NFC and MFC produced using the same methodology from a commercial sugarcane totally chlorine-free (TCF) soda–anthraquinone (soda–AQ) pulp served as a reference. Structural and physicochemical characterization involved optical transmittance, turbidity, conductimetry, X-ray diffraction, viscosity, FTIR, carboxyl content, cationic demand, degree of polymerization, and morphology by scanning electron microscopy (SEM). Results demonstrated that xylan and residual lignin contents influenced MFC formation, and the NFC showed properties comparable to those of the commercial pulp with fewer fibrillation passes. The study highlights GVL pulping as a greener, efficient alternative to conventional processes, opening new pathways for producing viscosity-controlled nanocellulose suspensions suitable for advanced applications. Full article

The traditional papermaking process uses petroleum-based additives, which raise environmental concerns. As a result, these concerns have attracted the scientific community to explore green additives by introducing environmentally friendly cellulose modifications as additives to the papermaking process. A promising way to process pulp is the application of deep eutectic solvent-like mixtures, which expand new possibilities for delignification processes. This article aims to characterize the physical properties of pulps modified with deep eutectic solvent-like mixtures and to compare these properties to untreated softwood kraft pulp and pulp obtained after oxygen delignification (commercially available pulp; obtained from Mondi Štětí a.s.). The physical properties (mechanical and optical) of the original pulp and delignified pulps were evaluated based on the degree of beating (Schopper–Riegler degree), zeta potential, water retention value, tensile strength, modulus of elasticity, and whiteness. Technology employing deep eutectic solvent-like mixtures shows great promise for sustainable pulp production; however, its full-scale adoption will require further research focused on process optimization, solvent recovery, and economic cost reduction. Full article

The natural variability and moisture sensitivity of bamboo limit its widespread use in construction applications. To address these challenges, densification and delignification processes have emerged as promising modification techniques. Densification and delignification processes can lead to significant improvements in the physical, mechanical, and chemical properties of solid wood. In this study, a two-step process of delignification and densification was carried out on Dendrocalamus asper bamboo specimens. The objective was to assess whether the optimized parameters of densification for natural bamboo on an open pressing system can be transferred for delignified bamboo. Delignification was achieved using an alkali solution (NaOH and Na₂SO₃) with two different temperature settings (25 °C or 100 °C). The pre-treated samples were dried in one of the two different conditions, either at 100 °C for 24 h or 25 °C for 30 days, resulting in four different groups with an average moisture content ranging from 7 to 10%. The samples were densified to 50% of their original thickness through an open thermo-mechanical press system at 160 °C with a compression rate of 6.7 mm/min and compared to densified bamboo without delignification (reference). The compression stress required to achieve a 50% degree of densification was evaluated, with untreated samples exhibiting an average value close to 17 MPa. Following treatment, the compression stress ranged from 7 to 13.4 MPa, indicating that the exposure to a high pH solution facilitates the densification process. However, a reduction in flexural properties (MOR, LOP, and MOE) was observed on the alkali-treated samples after a three-point bending test. Physical properties (water absorption and thickness swelling) were not altered after delignification. These findings demonstrate that the direct application of a densification process optimized for natural bamboo is not fully effective for chemically modified bamboo, highlighting the need for adjustments. Delignified bamboo showed an increase in free space after chemical treatment, which should be further densified under higher degrees. Full article

New sustainable materials have been developed to replace conventional plastics obtained from non-renewable sources. In this study, cellulose fibres from Posidonia oceanica (PO) were obtained by applying subcritical water extraction and bleaching with hydrogen peroxide or sodium chlorite. The PO fibres were used to obtain cellulose films, chitosan–cellulose composites, and PLA–cellulose laminates. These films were characterised as to their optical properties, mechanical performance, oxygen and water vapour permeability, thermal stability, and microstructure. The cellulose films exhibited low mechanical resistance, with different colouration depending on the degree of delignification. The composites had lower mechanical strength than pure chitosan films. The PO cellulose fibres had a similar, but attenuated, effect when laminated with PLA layers. The fibres improved the oxygen barrier capacity of chitosan films, although this effect only occurred in PLA laminates for cellulose purified with sodium chlorite. In no case did cellulose improve the water vapour barrier of the films compared to pure polymers. The thermal stability was not notably altered by the blending effect, thus reflecting the absence of significant interactions between the fibres and polymer. However, there is a need to improve the functionality of cellulose fibres from PO waste for their incorporation as fillers or laminates in biodegradable food packaging materials. Full article

(1) Background: The increasing generation of plastic and agricultural wastes is a critical environmental issue that requires urgent attention. Aiming to address this challenge, this study developed a sustainable waste-to-wealth system through the utilization of Zea mays husk as a reinforcing material in the production of green composites. (2) Methods: Delignification, de-hemicellulolysis, and bleaching were employed sequentially to improve the characteristics of the husk. Fourier-transform infrared spectroscopy and scanning electron microscopy confirmed the removal of lignin, hemicellulose, and impurities, and X-ray diffraction analysis determined the degree of crystallinity. Composites were made with treated and untreated husk and recycled low-density polyethylene (LDPE) at various husk-to-LDPE ratios. (3) Results: Mechanical characterization demonstrated that the treated husk composites exhibited superior tensile strength, flexural strength, and hardness compared to the untreated ones and pure LDPE. The treatment did not enhance the thermal stability of the composites, but it did lower their capacity for water absorption and improve their crystallinity. The economic assessment of the husk composite production indicated a total annualized cost of USD 0.9601 per kg, which is significantly lower than the estimated cost for LDPE (USD 1.2 to USD 1.4 per kg). Additionally, it has a much smaller carbon footprint compared to LDPE production. (4) Conclusions: The potential of utilizing treated Z. mays husk as a reinforcing agent in the development of sustainable and cost-effective green composites, improving their overall performance, was established. This approach offers a promising solution for the effective management of plastic and agricultural wastes, contributing to the transition towards a circular economy. Full article

Concerns on the expanding infestation of several Acacia species in the southern Mediterranean European countries have triggered an ever-growing requirement for costly targeted control actions. Valorizing biomass waste produced could help promote and better finance these actions. For that purpose, wood wastes from invasive control actions were tested regarding their pulp and paper potential, aiming to entice cellulose industries to partake in future conservation actions. Wood waste from the five most pervasive Acacia species was studied (Acacia dealbata Link, Acacia longifolia Willd, Acacia mearnsii De Wild, Acacia melanoxylon R.Br, and Acacia saligna Labill) regarding physical and chemical characteristics, and a central composite design was used to optimize alkali charge and reaction temperature on pulping yield and delignification. Bleached kraft pulps were produced with each species’ optimized conditions and for an equitable mixture of all species. Optimized pulp yields (52.6%–53.5%) and pulp polymerization degree (2867–3690) of Acacia species were higher than those of Eucalyptus globulus Labill (used as reference). Optimized bleached pulps were refined and fiber, pulp, and handsheet properties determined. Acacia dealbata and A. longifolia presented high specific wood consumption and lower handsheet strength properties, pointing to overall lower pulping potential, while A. melanoxylon and A. mearnsii characteristics were equal to or higher than those of E. globulus. A. saligna pulp and handsheet characteristics appear more suited for tissue paper. The Acacia mixture achieved acceptable characteristics, enabling the indiscriminate use of Acacia wood regardless of the species. As a shortcoming, the Acacia pulps showed the worst optical characteristics, with brightness dropping substantially with beating (64%–76%) when compared to E. globulus (81%). Full article

Sulfite and kraft pulping are two principal methods of industrial delignification of wood. In recent decades, those have been considered as possibilities to pretreat recalcitrant wood lignocellulosics for the enzymatic hydrolysis of polysaccharides and the subsequent fermentation of obtained sugars to valuable bioproducts. Current work compares chemistry and technological features of two different cooking processes in the preparation of polysaccharide substrates for deep saccharification with P. verruculosum glycosyl hydrolases. Bleached kraft and sulfite pulps were subjected to hydrolysis with enzyme mixture of high xylanase, cellobiohydrolase, and β-glucosidase activities at a dosage of 10 FPU/g of dry pulp and fiber concentration of 2.5, 5, and 10%. HPLC was used to analyze soluble sugars after hydrolysis and additional acid inversion of oligomers to monosaccharides. Kraft pulp demonstrated higher pulp conversion after 48 h (74–99%), which mostly resulted from deep xylan hydrolysis. Sulfite-pulp hydrolysates, obtained in similar conditions due to higher hexose concentration (more than 50 g/L), had higher fermentability for industrial strains producing alcohols, microbial protein, or organic acids. Along with saccharification, enzymatic modification of non-hydrolyzed residues occurred, which led to decreased degree of polymerization and composition changes in two industrial pulps. As a result, crystallinity of kraft pulp increased by 1.3%, which opens possibilities for obtaining new types of cellulosic products in the pulp and paper industry. The high adaptability and controllability of enzymatic and fermentation processes creates prospects for the modernization of existing factories. Full article

The combination of alkaline delignification and densification was applied to improve wood mechanical strength. Poplar wood samples were subjected to alkali delignification with varying degrees of lignin and hemicellulose removal followed by hot pressing. Dynamic mechanical performances and dynamic sorption behavior of the untreated and densified wood were then evaluated. Results showed that appropriate removal of lignin can improve the stiffness of densified wood and reduce moisture sorption and the numbers of sorption sites. Fourier transform infrared (FTIR) microscopy along with X-ray diffraction (XRD) were used to explain the viscoelastic and hygroscopicity of delignified and densified wood. Hemicelluloses and lignin were selectively dissolved during alkali treatment. Wood crystallinity was increased after alkali treatment at a moderate concentration of 2%, beneficial to improving the dimensional stability and mechanical performance of delignified and densified wood. The crosslinking of cellulose chains through hydrogen bonding, the decreased content of free hydroxyl groups, and the increased crystallinity in the cell wall contributed to higher storage modulus and lower hydrophilicity. The results support mild delignification and densification as a feasible way towards extending the service life of wood products used as structural materials. Full article

Pretreatment of sugarcane bagasse (SCB) by aqueous acetic acid (AA), with the addition of sulfuric acid (SA) as a catalyst under mild condition (<110 °C), was investigated. A response surface methodology (central composite design) was employed to study the effects of temperature, AA concentration, time, and SA concentration, as well as their interactive effects, on several response variables. Kinetic modeling was further investigated for AA pretreatment using both Saeman’s model and the Potential Degree of Reaction (PDR) model. It was found that Saeman’s model showed a great deviation from the experimental results, while the PDR model fitted the experimental data very well, with determination coefficients of 0.95–0.99. However, poor enzymatic digestibility of the AA-pretreated substrates was observed, mainly due to the relatively low degree of delignification and acetylation of cellulose. Post-treatment of the pretreated cellulosic solid well improved the cellulose digestibly by further selectively removing 50–60% of the residual linin and acetyl group. The enzymatic polysaccharide conversion increased from <30% for AA-pretreatment to about 70% for PAA post-treatment. Full article

The properties of the fibers determine the quality of the pulp and, thus, the quality of the paper made from it. Recognition of properties, which fiber and paper pulp should be characterized by, in order to achieve required paper properties, is, therefore, a subject of research and interest of many papermaking research experts and scientists. Fibers are subject to deformation and possible weakening under the influence of chemical and mechanical factors, and therefore the quality of the fibers decreases each time they are used in production when it comes to recycled pulps. Then again, the key factor determining the quality of the primary fiber is the degree of pulp delignification. In the article, an attempt was made to define the impact of delignification of virgin pulp on morphological properties of fibers, and compare them with the properties of recycled paper pulp, in order to find correlations. The current economic and raw material situations in the wood market force one to seek new solutions to limit the use of virgin fibers, which is extremely important for the economy of the paper mill, environmental protection and raw material management. Full article

The use of agricultural waste biomass for nanocellulose production has gained interest due to its environmental and economic benefits compared to conventional bleached pulp feedstock. However, there is still a need to establish robust process technologies that can accommodate the variability of waste feedstocks and to understand the effects of feedstock characteristics on the final nanofiber properties. Here, lignocellulosic nanofibers with unique properties are produced from various waste biomass based on a simple and low-cost process using mild operating conditions. The process robustness is demonstrated by diversifying the feedstock, ranging from food crop waste (corn stover) to invasive grass species (reed canary grass) and industrial lignocellulosic residues (industrial hemp). This comprehensive study provides a thorough examination of the influence of the feedstocks’ physico-chemical characteristics on the conversion treatment, including process yield, degree of delignification, effectiveness of nanofibrillation, fiber morphology, surface charge, and density. Results show that nanofibers have been successfully produced from all feedstocks, with minor to no adjustments to process conditions. This work provides a framework for future studies to engineer nanocellulose with specific properties by taking advantage of biomass feedstocks’ intrinsic characteristics to enable versatile applications. Full article

A new approach is being considered for obtaining microfibrillated cellulose with a low degree of polymerization by sulfuric acid hydrolysis with simultaneous ultrasonic treatment under mild conditions (temperature 25 °C, 80% power control). Samples of initial cellulose, MCC, and MFC were characterized by FTIR, XRF, SEM, DLS, and TGA. It was found that a high yield of MFC (86.4 wt.%) and a low SP (94) are observed during hydrolysis with ultrasonic treatment for 90 min. It was shown that the resulting microfibrillated cellulose retains the structure of cellulose I and has an IC of 0.74. It was found that MFC particles are a network of fibrils with an average size of 91.2 nm. ζ-potential of an aqueous suspension of MFC equal to −23.3 mV indicates its high stability. It is noted that MFC has high thermal stability, the maximum decomposition temperature is 333.9 °C. Simultaneous hydrolysis process with ultrasonic treatment to isolate MFC from cellulose obtained by oxidative delignification of spruce wood allows to reduce the number of stages, reduce energy costs, and expand the scope. Full article

Cryo-induced hydrogel from cellulose is a new class of biomaterials for drug delivery, cell delivery, bone and skin tissue engineering for cell proliferation and regeneration applications. This research aimed to synthesize cryo-induced hydrogel from cellulose and carboxymethyl cellulose (CMC) produced from empty bunch’s cell wall of Elaeis guineensis. First, the experiment was to produce cellulose-rich material using hot-compressed water extraction followed by alkaline delignification and bleaching with H₂O₂. The obtained bleached EFB cellulose was used as the substrate for CMC, and the optimal condition with the highest degree of carboxyl substitution (DS) of 0.75 was achieved when varying NaOH and monochloroacetic acid concentration as well as etherification temperature using fractional factorial design. For cryogelation study, hydrogels were synthesized from cellulose, CMC and beta-cyclodextrin (β-CD) by dissolving cellulose-based matrix in a NaOH/urea system, and the cellulose (CEL) solution was frozen spontaneously at −40 °C followed by high speed mixing to loosen cellulose fibrils. Epichlorohydrin (ECH) and Polyethylene glycol diglycidyl ether (PEGDE) were used as a cross-linker. First, the ratio of cellulose and CMC with different amounts of ECH was investigated, and subsequently the proper ratio was further studied by adding different crosslinkers and matrices, i.e., CMC and β-CD. From the result, the ECH crosslinked CMC-CEL (E-CMC-CEL) gel had the highest swelling properties of 5105% with the average pore size of lyophilized hydrogel of 300 µm. In addition, E-CMC-CEL gel had the highest loading and release capability of tetracycline in buffer solution at pH 7.4 and 3.2. At pH 7.4, tetracycline loading and release properties of E-CMC-CEL gel were 65.85 mg g⁻¹ dry hydrogel and 46.48 mg g⁻¹ dry hydrogel (70.6% cumulative release), respectively. However, at pH 3.2, the loading and release capabilities of Tetracycline were moderately lower at 16.25 mg g⁻¹ dry hydrogel and 5.06 mg g⁻¹ dry hydrogel, respectively. The findings presented that E-CMC-CEL hydrogel was a suitable material for antibiotic tetracycline drug carrying platform providing successful inhibitory effect on Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, respectively. Full article

Hydrogenation of flax shives in ethanol over bifunctional Ni/C catalysts at 225 °C has been studied. It has been shown that the 10% Ni/C catalyst enhances the yield of monomeric products from 1.1 to 9.7 wt %, decreases the solid product content from 45 to 35 wt %, and increases the degree of delignification to 91%. The main monomeric compounds obtained during hydrogenation are propyl guaiacol and propenyl guaiacol. It has been established that an increase in the mass transfer intensity via increasing the stirring rate or decreasing the catalyst grain size leads to an increase in the total yield of monomeric compounds and the propanol guaiacol yield. Alkaline and acid pretreatment increases the cellulose content in the solid product from 42 to 73 wt %. The proposed sequential scheme of the transformation and formation of monomeric products over the bifunctional nickel catalyst is lignin—coniferyl alcohol—4-propanol guaiacol—4-propenyl guaiacol—4-propyl guaiacol. Full article