Search Results (1,200)

Lodging is one of the key limiting factors in achieving high wheat yield. The application of plant growth retardants (PGRts) is regarded as an effective practice to prevent lodging. For accurate PGRt selection and the establishment of stable, high-yield production plans, it is essential to make clear the regulation strategies for lodging resistance and yield in PGRts. Field experiments were conducted at two test sites. At the initial jointing stage of wheat, Chlormequat Chloride (CCC) or Uniconazole (S₃₃₀₇) was sprayed. Compared with the control (CK), spraying CCC or S₃₃₀₇ significantly reduced the culm lodging index (CLI) and decreased the lodging rate from 7.1% to 15.6%. CCC was more capable of adjusting plant morphology (reducing plant height and second internode length and increasing stem diameter), while S₃₃₀₇ was more effective in enhancing breaking strength. The contents of GA, IAA, and zeatin nucleoside (ZR) and the activities of lignin-related enzymes (TAL and CAD) were significantly correlated with different stem indicators and CLI. Compared with CK, the yield after spraying CCC or S₃₃₀₇ increased by 6.5% and 6.0%, respectively. CCC mainly enhanced the yield by increasing grain weight per spike and the SPAD value of leaves, while S₃₃₀₇ mainly did so by increasing the number of spikes and the effective leaf area. Moreover, carbon metabolism-related enzymes (Rubisco, SS, and SPS) were significantly positively correlated with the yield. The enzyme activity of CCC was higher at the heading stage, while that of S₃₃₀₇ was higher at the filling stage. Hence, spraying CCC or S₃₃₀₇ can significantly enhance lodging resistance and yield. The optimal PGRts should be selected based on the climate and the growth stage of the wheat. Full article

This study investigates the development of biodegradable, scented bio-composite filaments incorporating industrial residues, specifically spent coffee grounds (SCG) and lignin (LI), into a PLA matrix for FDM 3D printing. Two fragrance additives, essential oil (EO) and microencapsulated fragrance powder (FP), were introduced (3%) to enhance sensory properties. The research investigates the effects of filler content (5%, 10%, and 15%) and fragrance additives on the surface chemistry (FTIR), thermal stability (TGA and DSC), mechanical properties (Tensile, flexural and impact), microstructure, and dimensional stability (Water absorption test and thickness swelling). Incorporating industrial residues and additives into PLA reduced the thermal stability, the degradation temperature and the glass transition temperature but increased the residual mass and the crystallinity. The effect of lignin was more pronounced than that of SCG, significantly influencing these thermal properties. Increasing the filler content of spent coffee grounds and lignin also led to a progressive decrease in tensile, flexural, and impact strength due to poor interfacial adhesion and increased void formation. However, lignin-based biocomposites exhibited enhanced stiffness at lower concentrations (≤10%), while biocomposites containing 15% SCG doubled their elongation at break compared to pure PLA. Adding fragrance reduced the mechanical strength but improved ductility due to plasticizer-like interactions. Microstructural analysis revealed heterogeneity in the biocomposites’ fracture surface characterized by the presence of pores, filler agglomeration, and delamination, indicating uneven filler dispersion and limited interfacial adhesion, particularly at high filler concentrations. The water absorption and dimensional stability of 3D-printed biocomposites increased progressively with the addition of residues. The presence of essential oil slightly improved water resistance by forming hydrogen bonds that limited moisture absorption. This article adds significant value by extending the potential applications of biocomposites beyond conventional engineering uses, making them particularly suitable for the fashion and design sectors, where multi-sensory and sustainable materials are increasingly sought after. Full article

Digital light processing (DLP) 3D printing is a powerful additive manufacturing technique but is limited by the relatively low mechanical strength of cured neat resin parts. In this study, a renewable bio-adhesive lignin was introduced as a reinforcing filler into a bisphenol A-type epoxy acrylate (EA) photocurable resin to enhance the mechanical performance of DLP-printed components. Lignin was incorporated at low concentrations (0–0.5 wt%), and three dispersion methods—magnetic stirring, planetary mixing, and ultrasonication—were compared to optimize the filler distribution. Cure depth tests and optical microscopy confirmed that ultrasonication (40 kHz, 5 h) achieved the most homogeneous dispersion, yielding a cure depth nearly matching that of the neat resin. DLP printing of tensile specimens demonstrated that as little as 0.025 wt% lignin increased tensile strength by ~39% (from 44.9 MPa to 62.2 MPa) compared to the neat resin, while maintaining similar elongation at break. Surface hardness also improved by over 40% at this optimal lignin content. However, higher lignin loadings (≥0.05 wt%) led to particle agglomeration, resulting in diminished mechanical gains and impaired printability (e.g., distortion and incomplete curing at 1 wt%). Fractographic analysis of broken specimens revealed that well-dispersed lignin particles act to deflect and hinder crack propagation, thereby enhancing fracture resistance. Overall, this work demonstrates a simple and sustainable approach to reinforce DLP 3D-printed polymers using biopolymer lignin, achieving significant improvements in mechanical properties while highlighting the value of bio-derived additives for advanced photopolymer 3D printing applications. Full article

Pinus massoniana, a critically important afforestation species in subtropical China, shows severe adventitious rooting recalcitrance linked to endogenous gibberellin (GA) dysregulation. Our study reveals a GA₄-mediated regulatory network that coordinates hormonal crosstalk, redox homeostasis, and cell wall remodeling. Treatment with the GA biosynthesis inhibitor paclobutrazol (PBZ, 100 mg·L⁻¹) shortened rooting time by 32.5% and increased rooting success by 79.5%. We found that PBZ redirected GA flux by upregulating GA₃-oxidase (GA₃OX), leading to GA₄ accumulation. However, elevated GA₄ levels impaired root development by triggering suberization through ferulic acid (FA)-mediated redox imbalance. Application of GA₄ (100 mg·L⁻¹) reduced caffeoyl alcohol content by 54.4% but increased FA and caffeic acid levels 2.4–3.9-fold, shifting lignin precursors toward suberin biosynthesis. FA modulated H₂O₂ flux in a dose-dependent manner: 200 mg·L⁻¹ optimized redox homeostasis (93.7% lower H₂O₂ influx), whereas 1000 mg·L⁻¹ suppressed mitosis. The combination of PBZ (100 mg·L⁻¹) and FA (200 mg·L⁻¹) synergistically enhanced rooting success by 34.4% and achieved 95.8% field survival after two years (vs. 68.5% in controls), challenging the traditional view that lignification alone limits rooting in woody plants. This work provides the first evidence that the GA₄-FA axis controls adventitious root formation in conifers via a Reactive oxygen species (ROS)-dependent switch between suberin and lignin metabolism, offering new strategies to overcome rooting barriers. The PBZ + FA protocol enables scalable clonal propagation of recalcitrant conifers, with potential applications in molecular breeding and forest restoration. Full article

A versatile, sustainable feedstock pathway to bio-based polymeric materials was developed utilizing lignin biomass and the ring-opening copolymerization (ROCOP) of cyclic anhydrides and epoxides to synthesize functional, lignin-derived, fully bio-based polyester polyols. The initial goal was to make the ROCOP reaction more applicable to bio-derived starting materials and more attractive to commercialization by conducting the polymerization under less constrained and industrially relevant conditions in air and without the extensive purification of reagents, catalysts, or solvents, typically used in the literature. A refined ROCOP system was applied as a powerful tool in lignin valorization by successfully synthesizing the lignin-derived copolyester prepolymers from lignin models and depolymerized native lignin sourced from the reductive catalytic fractionation of Pinus radiata wood biomass. After mechanistic studies based on NMR characterization, an alternative ROCOP-style mechanism was proposed. This was found to be (1) contributing to the acceleration of the observed reaction rates with added [PPNCl] organo-catalyst and (2) ‘self-initiation/self-promoted’ ROCOP without any added external [PPNCl] catalyst, likely due to the presence of inherent [OH] groups/ species in the lignin-derived glycidyl ether monomer promoting reactivity. As a final goal, the potential of these lignin-derived polyesters as intermediate polyols was demonstrated by applying them in the synthesis of polyurethane (PU) film materials with a high biomass content of 75–79%. A dramatic range of thermomechanical properties was observed for the resulting materials, demonstrating how the ROCOP reaction can be used to tailor the properties of the functional polyester and PU material based on the nature of the epoxide and anhydride substrates used. These findings help endeavors towards predicting the relationship between chemical structure and material thermomechanical properties and performance, relevant for industrial applications. Overall, this study demonstrated the proof of concept that PU materials can be prepared from lignocellulosic biomass utilizing industrially feasible ROCOP of bio-derived cyclic anhydrides and epoxides. Full article

Lignin-derived hard carbon (LHC) has emerged as a highly promising anode material for sodium-ion batteries (SIBs), owing to its renewable nature, structural tunability, and notable electrochemical properties. Although considerable advancements have been made in the development of LHCs in recent years, the absence of a comprehensive and critical review continues to impede further innovation in the field. To address this deficiency, the present review begins by examining the intrinsic characteristics of lignin and hard carbon (HC) to elucidate the underlying mechanisms of LHC microstructure formation. It then systematically categorizes the synthesis strategies, structural attributes, and performance influences of various LHCs, focusing particularly on how feedstock characteristics and fabrication parameters dictate final material behavior. Furthermore, optimization methodologies such as feedstock pretreatment, controlled processing, and post-synthesis modifications are explored in detail to provide a practical framework for performance enhancement. Finally, informed recommendations and future research directions are proposed to facilitate the integration of LHCs into next-generation SIB systems. This review aspires to deepen scientific understanding and guide rational design for improved LHC applications in energy storage. Full article

Forest biotechnology is rapidly advancing from conventional breeding toward molecular design, enabling the development of genetically modified trees (GMTs) with traits such as accelerated growth, stress resilience, and improved wood properties. This review systematically examines recent breakthroughs in tree genetic engineering, beginning with traditional methods and progressing to CRISPR-based precision editing and multi-omics-guided trait design. We highlight applications in wood quality (e.g., lignin reduction in Populus spp.), drought tolerance (e.g., PagHyPRP1 and PtoMYB142 editing), phytoremediation (e.g., heavy metal accumulation in poplar), and carbon sequestration. We also evaluate ecological and socio-regulatory challenges, including gene flow risks and public acceptance. Based on this integrated analysis, we outline future directions for responsible deployment of GMTs in sustainable forestry and global carbon neutrality efforts. Full article

Bacterial cellulose (BC) is a pure, crystalline biopolymer with broad applications, though large-scale production remains limited by the high cost of culture media. This study evaluated the use of artichoke bract waste as an alternative substrate for BC production by Komagataeibacter rhaeticus QK23, focusing on culture optimization and physicochemical characterization of the resulting biopolymer. Infrared spectroscopy revealed functional groups characteristic of cellulose, hemicellulose, lignin, and inulin, along with structural sugars (glucose 24%, xylose 5.07%, arabinose 4.96%, galactose 8.81%, and mannose 1.75%). After hydrolysis with H₂SO₄, up to 11.81 g/L of reducing sugars were released and incorporated into Hestrin–Schramm medium lacking glucose. Using a central composite design, inoculum dose (10–20%) and incubation time (7–14 days) were optimized under static conditions at 30 °C. The highest yield (1.57 g/L) was obtained with 20% inoculum after 14 days. The product corresponded to type I cellulose with a crystallinity index of 81.87%, and AFM analysis revealed a surface roughness of 32.96 nm. The results demonstrate that artichoke hydrolysates are a viable and sustainable source for BC production, promoting agricultural waste valorization and cost reduction in industrial biotechnology. Full article

The contamination of water resources by heavy metals poses a serious environmental risk, and conventional treatment methods face significant limitations. This review addresses the issue by presenting a critical analysis of the development of sustainable biosorbent and biopolymeric materials for heavy metal adsorption, highlighting advances, challenges, and future perspectives. To this end, a systematic bibliometric analysis of 120 documents was conducted, extracted from the Scopus and Web of Science databases, covering the period from 2003 to 2025. The results indicate exponential growth in scientific interest in biopolymers such as cellulose, chitosan, lignin, and alginate, especially in the form of aerogels, which demonstrate high adsorptive capacity through mechanisms such as complexation, chelation, and ion exchange. The analysis also reveals the main factors influencing process efficiency, such as pH, temperature, and contact time. It is concluded that, although these sustainable materials are highly promising, challenges related to scalability, selectivity in complex effluents, and regenerability still need to be overcome to enable their large-scale industrial application, in line with the principles of the circular economy. Full article

Cellulose stands out as a promising alternative to conventional polymers in food packaging due to its abundance, renewability, biodegradability and structural robustness. Despite these advantages, its natural low resistance to water and fats limits its direct application, necessitating the use of protective coatings to enhance its functionality. In this context, the use of biopolymeric coatings such as poly(lactic acid) (PLA), starch, lignin, chitin and chitosan has emerged as a sustainable solution, providing effective barriers against moisture and oils. These coatings not only improve the functional performance of cellulosic substrates but also reduce reliance on fossil-based plastics, fostering compostable systems and supporting a circular economy. This review analyzes recent developments in biopolymer-coated cellulosic packaging materials, focusing on their resistance to water and fats. The aim is to assess their potential for sustainable food packaging applications. The findings highlight how these innovations contribute to global sustainability goals, such as reducing plastic waste, lowering carbon emissions, and decreasing dependence on non-renewable resources. Full article

A depth study of optical, isothermal crystallization and mechanical properties was conducted on a series of poly(lactic acid) (PLA) nanocomposites based on lignin/multi-walled carbon nanotubes (MWCNTs) hybrid nanomaterial. The preparation was performed via solution casting followed by melt mixing. For comparison reasons, a group of PLA/lignin polymeric materials were prepared. Infrared spectroscopy (FTIR) did not reveal any significant impact on the main peaks of the nanocomposites by the incorporation of the additives. The optical properties were strongly affected by the content of the additive, as long as the thermal transitions parameters as evaluated from the differential scanning calorimetry (DSC) show important differences between cold and melt crystallization. X-ray diffraction (XRD) showed the semicrystalline behavior of the materials, while during isothermal crystallization experiments, the hybrid conductive nanomaterial acted as nucleation agent by promoting crystallization. Under evaluation of the mechanical properties, Young’s modulus tensile parameter increased significantly while the content of the hybrid nanomaterial increased, and the bending experiments of the materials with low content of the additives did not break. Thus, these substrates could be promising candidates for engineering applications, such as printed electronics. Full article

Lignin is one of the most abundant natural biopolymers and plays a crucial role in the development of safe and sustainable alternatives for healthcare products. In this study, we employed molecular dynamics simulations and free energy calculations to investigate lignin derivatives’ interactions with skin-like membranes. Specifically, we designed a small lignin derivative composed of syringyl and guaiacyl subunits. Our results reveal that molecular size, concentration, and thermal conditions critically influence the insertion, interaction dynamics, and localization behavior of lignin derivatives. Notably, variations in these parameters induce distinct behaviors, including rapid membrane insertion, hydrogen bonding, clustering, and surface adhesion. The findings provide insights into the molecular mechanisms governing lignin derivatives’ interactions with skin-like membranes, with implications for developing bio-based skincare formulations and transdermal delivery systems. Our results highlight the importance of molecular size and concentration in optimizing lignin-derived compounds for dermatological and therapeutic applications. Full article

Polymer-based aerogels have recently received considerable research attention as a favorable option for oil–water separation due to their enhanced porous 3D structure with great specific surface area, low density and outstanding sorption behavior. Additionally, polymer-containing aerogels exhibit more favorable characteristic properties, such as being lipophilic–hydrophobic (superhydrophobic–superoleophilic), hydrophilic–lipophobic (superhydrophilic–underwater oleophobic), or other specific wetness forms, including anisotropic and dual-wettability. In this review, cellulose and cellulose-based materials used as an aerogel for oil–water separation are comprehensively reviewed. This review highlights the significance of cellulose and cellulose-based combinations through structure–property interactions, surface modifications (using different hydrophilic and hydrophobic agents), and aerogel formation, focusing on the light density and high surface area of aerogels for effective oil–water separation. This article provides an in-depth review of four primary classifications of cellulose-based aerogels, namely, cellulose aerogels (regenerated cellulose and bacterial cellulose), cellulose with biopolymer-based aerogels (chitosan, lignin, and alginate), cellulose with synthetic polymer aerogels (polyvinyl alcohol, polyetherimide, polydopamine and others), and cellulose with organic/inorganic (such as SiO₂, MTMS, and tannic acid) material-based aerogels. Furthermore, the aspects of performance, scalability, and durability have been explained, alongside potential prospect directions for the advancement of cellulose aerogels aimed at their widespread application. This review article stands apart from previously published review works and represents the comprehensive review on cellulose-based aerogels for oil–water separation, featuring wide-ranging classifications. Full article

Starch is a promising alternative to petroleum-based polymers due to its biodegradability and renewable nature. However, its widespread use in non-food applications raises ethical concerns. Mango kernels, a major byproduct of mango processing, represent an abundant yet underutilized starch source. However, conventional starch extraction requires costly purification steps with significant environmental impact. This study explores the development of extruded biocomposites, using corn starch and mango kernel flour (MKF) as a more sustainable alternative. The influence of lignin, extractives, amylose, and amylopectin content on the material properties was assessed. MKF was obtained by removing both tegument and endocarp from the mango kernels, grinding them in a colloidal mill, and finally drying the ground kernels. The resulting flour was blended with corn starch, processed in an internal mixer, and injection-molded. The composites were characterized through mechanical testing, water absorption analysis, colorimetry, and UV absorption assays. Notably, the composite containing ~20% MKF exhibited mechanical properties comparable to commercial polyethylene (PE-PB 208), with a tensile strength of 9.53 MPa and a Young’s modulus of 241.41 MPa. Additionally, MKF enhanced UVA protection. These findings suggest that mango kernel flour can partially replace starch in the production of injection-molded biopolymers, offering a more sustainable approach to biodegradable plastic development. Full article

This study provides the first comprehensive multiscale evaluation of raw coconut fibers as biosorbents for crude oil removal, encompassing laboratory adsorption tests, mesoscale hydrodynamic simulations, and field trials in marine environments. Fibers were characterized by SEM, FTIR, XRD, XPS, and chemical composition analysis (NREL method), confirming their lignocellulosic nature, high lignin content, and functional groups favorable for hydrocarbon adsorption. At the microscale, a 2⁵⁻¹ fractional factorial design evaluated the influence of dosage, concentration, contact time, temperature, and pH, followed by kinetic and equilibrium model fitting and regeneration tests. Dosage, concentration, and contact time were the most significant factors, while low sensitivity to salinity highlighted the material’s robustness under marine conditions. Adsorption followed pseudo-second-order kinetics, with an equilibrium adsorption capacity of 4.18 ± 0.19 g/g, and it was best described by the Langmuir isotherm, indicating chemisorption and monolayer formation. Mechanical regeneration by centrifugation allowed for reuse for up to five cycles without chemical reagents, aligning with circular economy principles. In mesoscale and field applications, fibers maintained structural integrity, buoyancy, and adsorption efficiency. These results provide strong technical support for the practical use of raw coconut fibers in oil spill response, offering a renewable, accessible, and cost-effective solution for scalable applications in coastal and marine environments. Full article