Search Results (73)

The olive oil sector constitutes a fundamental pillar in the Mediterranean region from socio-economic and cultural perspectives. Nonetheless, it produces significant amounts of waste, leading to numerous environmental issues. These waste streams contain valuable compounds that can be recovered and utilized as inputs for various applications. This study introduces a novel value chain for olive wastes, focused on extracting lignin from olive pomace by ionic liquids and polyphenols from olive mill wastewater, which are then incorporated as hybrid nanoparticles in the formulation of an innovative starch-based biofertilizer. This biofertilizer, obtained by using residual wastewater as a source of soluble nitrogen, acting at the same time as a plasticizer for the biopolymer, was demonstrated to surpass traditional NPK biofertilizers’ efficiency, allowing for root growth and foliage in drought conditions. In order to recognize the environmental impact due to its production and align it with the technical output, the circularity and environmental performance of the proposed system were innovatively evaluated through a combination of Life Cycle Assessment (LCA) and the Material Circularity Indicator (MCI). LCA results indicated that the initial upcycling process was potentially characterized by significant hot spots, primarily related to energy consumption (>0.70 kWh/kg of water) during the early processing stages. As a result, the LCA score of this preliminary version of the biofertilizer may be higher than that of conventional commercial products, due to reliance on thermal processes for water removal and the substantial contribution (56%) of lignin/polyphenol precursors to the total LCA score. Replacing energy-intensive thermal treatments with more efficient alternatives represents a critical area for improvement. The MCI value of 0.84 indicates limited potential for further enhancement. Full article

The increasing demand for sustainable and environmentally friendly materials has prompted intensive research into developing bioplastics as viable alternatives to conventional petroleum-derived plastics. Here, we report a novel approach to bioplastic production by employing plant extract-based solvents to partially dissolve cellulose, a fundamental biopolymer precursor. Using plant-derived solvents addresses concerns surrounding the environmental impact of traditional solvent-based processes, as per the principles of green chemistry. Using computational screening, some natural products were identified from the integrated database resource MEGx. Six natural sources were selected based on their molecular weight, high pKa, and chemical classification. Thin-layer chromatography (TLC) and column chromatography confirmed the presence of molecules in the extracts. Bioplastics were prepared with 1, 3, 6, 10, and 15 wt.% plant extract concentrations. Control samples without conventional dissolved and positive controls were also studied to compare their properties with novel bioplastics. Chemical characterization and biodegradability tests were performed. Degradation in water and soil tests for 35 days showed that the biodegradability of the bioplastics with natural extracts at higher concentrations was faster than that of the control samples. By day 35, bioplastics containing 15 wt.% of the D1 W extract showed rapid degradation, with higher weight loss compared with the conventional controls. The positive control (C4), containing NaOH and glycerol, degraded more slowly than the plant extract-based formulations. Also, the test indicated that the natural dissolvent’s influence on the water uptake of the material produced a better performance than the control samples. The surfaces of the bioplastic formulations were analyzed using a scanning electron microscope (SEM) at different magnifications. The findings presented here hold promise for advancing the field of bioplastics and contributing to the sustainable utilization of plant resources for eco-friendly material production. Full article

Hierarchical porous carbon materials hold great potential for energy storage applications due to their high porosity, large specific surface area, and excellent electrical conductivity. Cellulose and sodium alginate are naturally abundant high-molecular-weight biopolymer materials. Utilizing them as precursors for the fabrication of high-performance electrochemical carbon materials is highly significant for achieving carbon neutrality goals. In this study, porous carbon aerogels were successfully synthesized using a combination of freeze-drying and a simple carbonization process, with nanocellulose and sodium alginate as precursors. Among the prepared samples, SC-0.03 (sodium alginate: nanocellulose = 0.1:0.03) exhibited the best performance, achieving a specific surface area of 713.7 m² g⁻¹. This material features an optimized hierarchical pore structure and a substantial intrinsic oxygen doping content, resulting in excellent capacitance performance. Benefiting from these structural advantages and their synergistic effects, the SC-0.03 electrode demonstrated a high specific capacitance of 251.5 F g⁻¹ at a current density of 0.5 A g⁻¹. This study shows that the construction of three-dimensional porous structures by taking advantage of the self-supporting properties of natural polymer materials does not require the introduction of external binders. Due to the nanoscale dimensions and high aspect ratio, nanocellulose enables the formation of a more refined and interconnected hierarchical pore network, enhancing ion accessibility and conductivity. The hierarchical porous carbon aerogel developed in this study, based on a biomass self-reinforcement strategy, not only shows great promise as an advanced energy storage material but also possesses environmentally friendly properties, offering new insights for the development of sustainable energy materials. Full article

The demand for drinking water is a reality that plagues modern society and will worsen in the coming decades. Factors such as climate change, population growth, and intense, often disorderly urbanization are expected to limit the availability of this essential resource for life. With this justification, several technologies involving water remediation/purification have been improved to increase energy efficiency. One key approach involves the use of residual biomass derived from biological sources as adsorbents with valuable properties. This line of research supports waste management, and the materials are easily obtainable, especially on a large scale, with low costs and negligible secondary environmental impacts. In the early 2000s, it was demonstrated that these materials possess functional groups (amino, hydroxyl, and carboxyl) that are favorable for attracting certain pollutants that are present in wastewater. Generally, the unmodified precursor material has properties that are not favorable for adsorption, such as limited adsorption capacity, low mechanical resistance, and unstable surface chemistry. Therefore, there has been a strong investment in studies aimed at developing methodologies to produce bio-based materials with high properties supported by mathematical models aimed at water purification. This critical review describes the modifications, functionalization, and production of bio-based materials aimed at remediating wastewater via the adsorption process. Their use involves the elimination of organic pollutants, water/oil separation, the removal of micropollutants, and membrane filtration. The properties of bio-based materials from biopolymers and their synthesis methodologies are analyzed, with a focus on water remediation. Finally, the challenges and future perspectives are highlighted, highlighting the relevance of this group of adsorbents in minimizing the challenges and limitations present in the field of water purification and providing new, innovative solutions. Full article

Among the various contenders for next-generation sodium-ion battery anodes, hard carbons stand out for their notable reversible capacity, extended cycle life, and cost-effectiveness. Their economic advantage can be further enhanced by using inexpensive precursors, such as biomass waste. Lignin, one of the most abundant natural biopolymers on Earth, which can be readily obtained from wood, possesses a three-dimensional amorphous polymeric structure, making it a suitable candidate for producing carbonaceous materials through appropriate carbonization processes for energy storage applications. In this work, we synthesized hard carbon using lignin containing CaSO₄ to facilitate partial catalytic graphitization to improve the microstructural features, such as interlayer spacing, degree of disorder, and surface defects. Partial catalytic graphitization enables hard carbon to develop an ordered structure compared with hard carbon carbonized without CaSO₄ as analyzed by X-ray diffraction, Raman spectroscopy, scanning/transmission electron microscopy, and X-ray photoelectron spectroscopy. The CaSO₄-aided partially catalytic graphitized hard carbon (CCG-HC) exhibited improved electrochemical performance, showing a larger portion of the low-voltage plateau—an indicator typically associated with a highly ordered structure—compared to simply carbonized hard carbon (HC). Notably, CCG-HC delivered a reversible capacity of 237 mAh g⁻¹, retained 95.6% of its capacity over 100 cycles at 50 mA g⁻¹, and exhibited 127 mAh g⁻¹ at 1.0 A g⁻¹. Full article

Polysaccharides represent the most abundant biopolymers in agri-food wastes and thus are the most studied polymers to produce biodegradable films for use in packaging. Starch is among the major polysaccharides extracted from food and agricultural waste that have been used as precursor material for film production. Therefore, the present study aimed at producing an active film with antimicrobial properties using starch extracted from cassava waste and oil extracted from cloves. The antimicrobial activity of the produced films was tested against Staphylococcus aureus, Salmonella Typhimurium and Listeria monocytogenes. Cassava periderm and cortex were bleached with either NaClO or H₂O₂ before starch aqueous extraction. The active films’ antimicrobial effectiveness was assessed by the formation of inhibitory halos around film disc samples in an agar diffusion method. The inhibition zone diameters were statistically similar for all microorganisms, with an average diameter of 11.87 ± 1.62 mm. The films presented an average water vapor permeability of 0.14 g mm/m² h kPa, an average tensile strength of 0.17 MPa and an elongation at break of 32.90%. Based on the determined properties, the produced films were deemed adequate for use in food packaging, in which antimicrobial activity is paramount. Full article

Novel photocatalysts were synthesized through the association of carbon quantum dots (CQDs) with commercial (P25) titanium dioxide (TiO₂) by sonication. The resulting TiO₂/CQDs composite was then incorporated into the polyamide 66 (PA66) biopolymer nanofibers using the electrospinning technique, considering a composite nanoparticles-to-polymer ratio of 1:2 in the electrospinning precursor solution. The produced nanofibers presented suitable morphology and were tested for the photocatalytic degradation under simulated solar radiation of 10 mg L⁻¹ of amoxicillin (AMX) and sulfadiazine (SDZ), in phosphate buffer solution (pH 8.06) and river water, using 1.5 g L⁻¹ of photocatalyst. The presence of the photocatalyst increased the removal of AMX in phosphate buffer solution by 30 times, reducing the AMX degradation half-life time from 62 ± 1 h (without catalyst) to 1.98 ± 0.06 h. Moreover, SDZ degradation half-life time in phosphate buffer solution was reduced from 5.4 ± 0.1 h (without catalyst) to 1.87 ± 0.05 h in the presence of the photocatalyst. Furthermore, the PA66/TiO₂/CQDs were also efficient in river water samples and maintained their performance in at least three cycles of SDZ photodegradation in river water. The presented results evidence that the produced photocatalyst can be a promising and sustainable solution for antibiotics’ efficient removal from water. Full article

The haloarchaeon Haloferax mediterranei synthesizes poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) under unfavorable nutritional conditions without the addition of any precursor to the culture, which is an advantage compared to other microbial counterparts able to synthesize polyhydroxyalkanoates (PHA). PHBV is a biodegradable polymer showing physiochemical properties of biotechnological and biomedical interest and can be used as an alternative to plastics made from chemical synthesis (which are not environmentally friendly). The versatile metabolism of H. mediterranei makes the use of waste as a carbon source for cellular growth and PHA synthesis possible. In this work, cellular growth and the production and characterization of PHBV using two different types of confectionery waste were analyzed and compared with cellular growth and PHBV synthesis in a standard culture media with glucose of analytical grade as a carbon source. The PHBV granules produced were analyzed by TEM and the biopolymer was isolated and characterized by GC-MS, FTIR NMR, and DSC. The results reveal that H. mediterranei can use these two residues (R1 and R2) for pure PHBV production, achieving 0.256 and 0.983 g PHBV/L, respectively, which are among the highest yields so far described using for the first-time waste from the candy industry. Thus, a circular economy-based process has been designed to optimize the upscaling of PHBV production by using haloarchaea as cell factories and valorizing confectionery waste. Full article

With the increased need for improved adsorbents for efficient water treatment, sodium alginate (NaAlg) and chitosan (Chi) represent promising platform biopolymers for the preparation of biocomposite adsorbents for the effective removal of waterborne oxyanion (arsenate (As_i) and orthophosphate (P_i)) contaminants. The TMCs were characterized by spectroscopy (infrared (IR), SEM with an energy dispersive X-ray (SEM-EDX)), point-of-zero-charge (PZC) measurements, and dye adsorption by employing p-nitrophenol at variable pH. Based on dye adsorption results, the adsorbent surface area (SA) was 271 m²/g for Al-TMC, 286 m²/g for Fe-TMC, and 311 m²/g for Cu-TMC. This indicates the role of adsorbent pore structure and swelling in water. Further, the role of either aluminum (Al), copper (Cu), or iron (Fe) for the preparation of TMCs for the selective As_i removal in the presence of P_i as a competitor anion was evaluated. While Al, Fe, and Cu coordinate to the biopolymer framework at C=O sites, only Fe coordinates to –NH₂ sites. While Al coordinated via Al-O and interfacial hydroxy groups, Cu showed the formation of Cu₂(OH)₃NO₃ in contrast to Fe, which observed FeOOH formation. Adsorption of As_i was highest for Al-TMC (80 mg/g), followed by Fe-TMC (77 mg/g) and Cu-TMC (31 mg/g). Adsorption of P_i was highest for Al-TMC (93 mg/g), followed by Fe-TMC (66 mg/g) and Cu-TMC (17 mg/g). While Al-TMC showed the highest adsorption capacity overall, only Fe-TMC (followed by Cu-TMC) showed strong arsenate selectivity over orthophosphate. The selectivity toward As_i in presence of P_i was determined and the binary separation factor (α_t/c) and the selectivity coefficient (β_t) were calculated, where Cu-TMC (α_t/c = 6.1; β_t = 4.4) and Fe-TMC (α_t/c = 8.3; β_t = 5.0) exceeded Al-TMC (α_t/c = 1.5; β_t = 1.2). This work contributes to the field of oxyanion-selective adsorbents via judicious selection of the metal salt precursor during the synthetic design of the ternary biocomposite systems, as demonstrated herein. Full article

Hydroxyapatite (HAp) polymer composites have gained significant attention due to their applications in bone regeneration and tooth implants. This review examines the synthesis, properties, and applications of Hap, highlighting various manufacturing methods, including wet, dry, hydrothermal, and sol–gel processes. The properties of HAp are influenced by precursor materials and are commonly obtained from natural calcium-rich sources like eggshells, seashells, and fish scales. Composite materials, such as cellulose–hydroxyapatite and gelatin–hydroxyapatite, exhibit promising strength and biocompatibility for bone and tissue replacement. Metallic implants and scaffolds enhance stability, including well-known titanium-based and stainless steel-based implants and ceramic body implants. Biopolymers, like chitosan and alginate, combined with Hap, offer chemical stability and strength for tissue engineering. Collagen, fibrin, and gelatin play crucial roles in mimicking natural bone composition. Various synthesis methods like sol–gel, hydrothermal, and solution casting produce HAp crystals, with potential applications in bone repair and regeneration. Additionally, the use of biowaste materials, like eggshells and snails or seashells, not only supports sustainable HAp production but also reduces environmental impact. This review emphasizes the significance of understanding the properties of calcium–phosphate (Ca-P) compounds and processing methods for scaffold generation, highlighting novel characteristics and mechanisms of biomaterials in bone healing. Comparative studies of these methods in specific applications underscore the versatility and potential of HAp composites in biomedical engineering. Overall, HAp composites offer promising solutions for improving patient outcomes in bone replacement and tissue engineering and advancing medical practices. Full article

Lignocellulose is a major biopolymer in plant biomass with a complex structure and composition. It consists of a significant amount of high molecular aromatic compounds, particularly vanillin, syringeal, ferulic acid, and muconic acid, that could be converted into intracellular metabolites such as polyhydroxyalkanoates (PHA) and hydroxybutyrate (PHB), a key component of bioplastic production. Several pre-treatment methods were utilized to release monosaccharides, which are the precursors of the relevant pathway. The consolidated bioprocessing of lignocellulose-capable microbes for biomass depolymerization was discussed in this study. Carbon can be stored in a variety of forms, including PHAs, PHBs, wax esters, and triacylglycerides. From a biotechnology standpoint, these compounds are quite adaptable due to their precursors’ utilization of hydrogen energy. This study lays the groundwork for the idea of lignocellulose valorization into value-added products through several significant dominant pathways. Full article

The utility of brewery spent grain (BSG), a byproduct of the beer production process, for the synthesis of polyhydroxyalkanoates (PHAs), is a significant advancement towards sustainable and cost-effective biopolymer production. This paper reviews the upcycling potential of BSG as a substrate for PHA production, utilizing various biotechnological approaches to convert this abundant waste material into high-value biodegradable polymers. Through a comprehensive review of recent studies, we highlight the biochemical composition of BSG and its suitability for microbial fermentation processes. This research delves into different methodologies for PHA production from BSG, including the use of mixed microbial cultures (MMCs) for the synthesis of volatile fatty acids (VFAs), a critical precursor in PHA production, and solid-state fermentation (SSF) techniques. We also examine the optimization of process parameters such as pH, temperature, and microbial concentration through the application of the Doehlert design, revealing the intricate relationships between these factors and their impact on VFA profiles and PHA yields. Additionally, this paper discusses challenges and future perspectives for enhancing the efficiency and economic viability of PHA production from BSG. By harnessing the untapped potential of BSG, this research contributes to the development of a circular economy model, emphasizing waste valorization and the creation of sustainable alternatives to conventional plastics. Full article

Poly-γ-glutamic acid (γ-PGA) is an attractive biopolymer for medical, agri-food, and environmental applications. Although microbial synthesis by Bacilli fed on waste streams has been widely adopted, the obtainment of efficient sustainable production processes is still under investigation by bioprocess and metabolic engineering approaches. The abundant glycerol-rich waste generated in the biodiesel industry can be used as a carbon source for γ-PGA production. Here, we studied fermentation performance in different engineered Bacillus subtilis strains in glycerol-based media, considering a swrA⁺ degU32^Hy mutant as the initial producer strain and glucose-based media for comparison. Modifications included engineering the biosynthetic pgs operon regulation (replacing its native promoter with P_hyspank), precursor accumulation (sucCD or odhAB deletion), and enhanced glutamate racemization (racE overexpression), predicted as crucial reactions by genome-scale model simulations. All interventions increased productivity in glucose-based media, with P_hyspank-pgs ∆sucCD showing the highest γ-PGA titer (52 g/L). Weaker effects were observed in glycerol-based media: ∆sucCD and P_hyspank-pgs led to slight improvements under low- and high-glutamate conditions, respectively, reaching ~22 g/L γ-PGA (26% increase). No performance decrease was detected by replacing pure glycerol with crude glycerol waste from a biodiesel plant, and by a 30-fold scale-up. These results may be relevant for improving industrial γ-PGA production efficiency and process sustainability using waste feedstock. The performance differences observed between glucose and glycerol media also motivate additional computational and experimental studies to design metabolically optimized strains. Full article

Renewable, green, and safe natural biopolymer-derived materials are highly desired for the purification of pollutants, but significantly improving their performance without the introduction of additional harmful chemicals remains a huge challenge. Based on the concept of “structure optimization design”, environment-friendly composite beads (named SA/PASP/RE) with excellent adsorption performance and recyclability were rationally constructed through a green ionic crosslinking route, using the completely green biopolymer sodium alginate (SA), sodium salt of polyaspartic acid (PASP), and the natural nanoclay rectorite (RE) as starting materials. The nano-layered RE was embedded in the polymer matrix to prevent the polymer chain from becoming over-entangled so that more adsorption sites inside the polymer network were exposed, which effectively improved the mass transfer efficiency of the adsorbent and the removal rate of contaminants. The composite beads embedded with 0.6% RE showed high adsorption capacities of 211.78, 197.13, and 195.69 mg/g for Pb(II) and 643.00, 577.80, and 567.10 mg/g for methylene blue (MB) in Yellow River water, Yangtze River water, and tap water, respectively. And the beads embedded with 43% RE could efficiently adsorb Pb(II) and MB with high capacities of 187.78 mg/g and 586.46 mg/g, respectively. This study provides a new route to design and develop a green, cost-effective, and efficient adsorbent for the decontamination of wastewater. Full article

Kynurenic acid (KYNA) is a bioactive compound exhibiting multiple actions and positive effects on human health due to its antioxidant, anti-inflammatory and neuroprotective properties. KYNA has been found to have a beneficial effect on wound healing and the prevention of scarring. Despite notable progress in the research focused on KYNA observed during the last 10 years, KYNA’s presence in flax (Linum usitatissimum L.) has not been proven to date. In the present study, parts of flax plants were analysed for KYNA synthesis. Moreover, eight different cultivars of flax seeds were tested for the presence of KYNA, resulting in a maximum of 0.432 µg/g FW in the seeds of the cultivar Jan. The level of KYNA was also tested in the stems and roots of two selected flax cultivars: an oily cultivar (Linola) and a fibrous cultivar (Nike). The exposure of plants to the KYNA precursors tryptophan and kynurenine resulted in higher levels of KYNA accumulation in flax shoots and roots. Thus, the obtained results indicate that KYNA might be synthesized in flax. The highest amount of KYNA (295.9 µg/g dry weight [DW]) was detected in flax roots derived from plants grown in tissue cultures supplemented with tryptophan. A spectroscopic analysis of KYNA was performed using the FTIR/ATR method. It was found that, in tested samples, the characteristic KYNA vibration bands overlap with the bands corresponding to the vibrations of biopolymers (especially pectin and cellulose) present in flax plants and fibres. Full article