Search Results (173)

The urgent need for bio-based functional materials has driven a shift away from fossil-fuel-sourced materials toward renewable lignocellulosic biomass (LCB). This comprehensive review explores the advancements in LCB carbonization between 2020 and 2026, marking a shift from traditional, low-yield combustion processes toward highly selective and sustainable thermochemical conversion pathways. The primary objective of this review is to evaluate the integration of green pretreatment strategies, conversion technologies, and efficient valorization of the aqueous effluents and by-products. The goal of green pretreatment is to overcome the inherent recalcitrance of LCB without the use of harsh chemicals and reaction conditions, specifically highlighting the effectiveness of deep eutectic solvents (DESs) and ionic liquids (ILs). The review also evaluates the emerging conversion technologies, including hydrothermal carbonization (HTC), microwave-assisted pyrolysis (MAP), and the synergistic co-pyrolysis of LCB with synthetic polymeric wastes. Another novel concept in preparing hard carbon and other related materials is the “lignin-first” biorefinery strategy, which facilitates the subsequent production of high-value aromatic monomers, platform chemicals, and biofuels. The engineered carbon materials are increasingly utilized well beyond their traditional use as solid fuels. The products have been proven to be excellent for use in high-performance energy conversion and storage, serving as renewable bio-based electrode materials for supercapacitors and carbon electrodes in next-generation batteries. Full article

There is growing demand for biosourced functional polymers, particularly in organic electronics, which continue to rely heavily on petroleum-derived materials. In this regard, platform chemicals obtained from biomass offer sustainable alternatives. However, the development of biosourced polymers prepared by metal-free methods remains limited. In this context, lignin-derived divanillin is an attractive renewable unit that can be incorporated into polymer backbones. This work discusses the synthesis and characterization of a new family of biosourced divanillin-based polymers prepared through metal-free aldol polycondensation. Divanillin was obtained from biosourced vanillin and converted into two dialdehyde monomers bearing either methyl or decyl substituents. These monomers were polymerized via aldol polycondensation, affording the following polymers: PDVMeCP, PDVMeCH, PDVMeIND, and PDVC10IND. The influence of the cyclic ketone unit and side-chain structure on their thermal and optical properties was investigated. The polymers were soluble in common organic solvents and also showed solubility in greener solvents such as ethyl L-lactate and p-cymene. Optical and electrochemical analyses showed absorption maxima between 357 and 391 nm and electronic bandgaps from 1.84 to 2.14 eV. Overall, the results demonstrate that divanillin is a promising renewable building block for the metal-free synthesis of sustainable polymers. Full article

Viscosity reducers are essential additives for water-based drilling fluids (WBDFs), serving to counteract the rheological degradation induced by the high-temperature and high-salinity conditions commonly encountered in deep and ultra-deep well drilling. This paper systematically reviews the research progress in this field, categorizing viscosity reducers into three major systems: modified natural materials, industrial waste utilization, and synthetic polymers. Modified natural material viscosity reducers, derived from renewable materials such as lignin and humic acid via chemical modification, are environmentally friendly products. The preparation of viscosity reducers from industrial wastes realizes both resource recycling and economic benefits. Synthetic polymer viscosity reducers, incorporated with functional monomers such as sulfonic and carboxylic groups, achieve high performance with temperature resistance exceeding 220 °C as well as excellent salt and calcium tolerance via rational molecular design, and represent the current mainstream research direction in the field. This paper provides an in-depth analysis of the action mechanisms of various viscosity reducers, summarizes the performance characteristics, synthesis methods and application status, and identifies challenges in structure–property relationship elucidation, extreme working condition adaptability, and technology transfer efficiency. Finally, future development trends are discussed, with emphasis on precision molecular design, ultimate performance requirements for ultra-deep wells, environmentally sustainable approaches, and the establishment of standardized evaluation protocols. This review aims to provide both theoretical insights and practical guidance to support the efficient development of deep oil and gas resources. Full article

Driven by the growing demand for sustainable polymers, polylactic acid (PLA) has attracted increasing attention due to its renewable origin and biodegradability. Lactide, the key cyclic monomer for PLA production via ring-opening polymerization (ROP), plays a decisive role in determining the molecular weight, stereoregularity, and final performance of PLA materials. However, current lactide synthesis processes still face significant challenges, including competing side reactions under high-temperature and high-vacuum conditions, difficulties in controlling stereochemical purity, and relatively high energy consumption. In this review, recent advances in lactide synthesis are systematically analyzed by examining the two principal industrial routes: the one-step process based on the direct dehydration–cyclization of lactic acid (LA), and the two-step process involving prepolymerization of LA followed by depolymerization/cyclization of oligomeric intermediates. The reaction mechanisms, key intermediates, and major side reactions—including racemization, transesterification, and deep polycondensation—are discussed, together with the regulatory roles of catalytic systems and reaction–separation coupling strategies. Comparative analysis reveals that the one-step route offers advantages in process integration and potential energy efficiency, whereas the two-step route provides superior control over stereochemical purity and process stability. Future research directions focusing on green catalysts, process intensification, and sustainable lactide production are also highlighted. Full article

Plastic manufacturing depends heavily on petroleum-derived monomers like terephthalic acid, the main component of polyethylene terephthalate (PET). However, the depletion of fossil resources and increasing environmental concerns have heightened the need for sustainable alternatives. Lignocellulosic biomass has emerged as a promising resource due to its renewable, abundant, and eco-friendly nature. Understanding its chemical composition enables conversion of this biomass into platform chemicals, such as 2,5-furandicarboxylic acid (FDCA) and lactic acid, derived from cellulose and hemicellulose. These can be polymerized into bio-based plastics such as polyethylene furanoate (PEF), polylactic acid (PLA), and polyhydroxyalkanoates (PHAs), offering greener alternatives to fossil-based plastics. PEF features rigid furan rings that enhance thermal stability, mechanical strength, and barrier properties, and reduce gas permeability compared to PET. PLA is a renewable, biodegradable plastic widely used in packaging and medical applications. This review covers the chemical composition of lignocellulosic biomass cellulose, hemicellulose, and lignin, and various pretreatment strategies, chemical, physicochemical, and physical, to overcome biomass recalcitrance and improve conversion efficiency. It also highlights recent catalytic advances in transforming cellulosic carbohydrates into bio-based plastic precursors such as FDCA and lactic acid. Lastly, this review discusses polymerization pathways for producing PEF and PLA, emphasizing their role in reducing the environmental impact of polymer manufacturing and promoting green chemistry principles. Full article

Plastics are highly persistent materials, and their environmental degradation can potentially exacerbate, rather than alleviate, pollution. The degradation of plastic materials releases toxic monomers and additives, such as bisphenol A (BPA), styrene, and dioxins, which are more reactive, harmful, and persistent than intact plastics. With half-lives ranging from weeks to decades, they bioaccumulate in food chains, disrupt ecosystems, and contribute to endocrine disruption and mutagenicity. Natural degradation pathways, like microbial metabolism and photodegradation, are slow and incomplete, often leaving toxic intermediates such as microplastics. Artificial strategies, including bioremediation and advanced oxidation processes (AOPs), show potential to address the problems of plastic pollution but face additional challenges like secondary pollution and scalability. Sustainable alternatives, including bioplastics and renewable non-plastic substitutes, present promising solutions. However, their widespread adoption is hindered by challenges such as high production costs and the need for specific conditions to facilitate degradation, necessitating further research and development. A combined approach of reducing plastic production, advancing recycling, and implementing effective remediation strategies is critical to mitigating plastic pollution’s long-term impacts on ecosystems, biodiversity, and human health. This review provides a critical analysis of the current understanding of plastic degradation processes and the toxic byproducts they generate. It highlights the paradox wherein increased degradability may exacerbate environmental hazards. Additionally, the review assesses innovative, eco-friendly alternatives designed to mitigate plastic pollution. Full article

Lignin is a complex aromatic polymer that constitutes a major fraction of plant biomass and represents a valuable renewable carbon resource. Naturally decaying wood serves as an environmental reservoir of microorganisms capable of degrading lignin. In this study, we isolated and characterized sixteen bacterial strains from decaying Tilia cordata wood using an enrichment culture technique with lignin as the sole carbon source. Taxonomic identification via 16S rRNA gene sequencing revealed microbial diversity spanning the genera Bacillus, Pseudomonas, Stenotrophomonas, and several members of the Enterobacteriaceae family, including Raoultella terrigena isolates. Metagenomic sequencing of the wood substrate revealed an exceptionally rich and balanced bacterial community (Shannon index H′ = 5.07), dominated by Streptomyces, Bradyrhizobium, Bacillus, and Pseudomonas, likely reflecting a specialized consortium adapted to lignin rich late-stage decay. Functional phenotyping demonstrated that all isolates possess ligninolytic potential, evidenced by peroxidase/laccase-type activity through methylene blue decolorization. Dynamic Light Scattering (DLS) and HPLC analyses showed that some isolates, such as Raoultella terrigena MGMM806, effectively depolymerized lignosulfonate into low molecular weight fragments (1.23 nm), while others accumulated intermediate metabolites or completely mineralized the substrate. Growth profiling on monolignol substrates revealed a broad spectrum of catabolic specialization in lignin monomer degradation. The results demonstrate a complex system of metabolic partitioning within a natural bacterial consortium. This collection represents a foundational genetic resource for developing engineered biocatalysts and synthetic microbial communities aimed at the efficient conversion of lignin into valuable aromatic compounds. Full article

Polyurethanes (PUs) are indispensable polymeric materials widely employed across diverse industrial sectors due to their excellent thermal stability, chemical resistance, adhesion, and mechanical durability. However, the intrinsic three-dimensional crosslinked network that underpins their performance also presents a fundamental barrier to reprocessing and recycling. Consequently, most end-of-life PU waste is currently managed through landfilling or incineration, resulting in significant resource loss and environmental impact. To address these challenges, this review presents an integrated perspective on sustainable PU systems by unifying green synthesis strategies with closed-loop recovery approaches. First, recent advances in bio-based polyols and phosgene-free isocyanate synthesis derived from renewable resources—such as plant oils, carbohydrates, and lignin—are discussed as viable means to reduce dependence on petrochemical feedstocks and mitigate toxicity concerns. Next, emerging chemical recycling methodologies, including acidolysis and aminolysis, are reviewed with a focus on the selective recovery of high-purity monomers. Finally, PU vitrimers and dynamic covalent polymer networks (DCPNs) based on urethane bond exchange reactions are examined as reprocessable architectures that combine thermoplastic-like processability with the mechanical robustness of thermosets. By integrating synthesis, recovery, and reuse within a unified framework, this review aims to outline a coherent pathway toward establishing a sustainable circular economy for PU materials. Full article

Agricultural biomass has potential as a renewable and versatile carbon feedstock for developing eco-friendly and biodegradable polymers capable of replacing conventional petrochemical plastics. To address the growing environmental concerns associated with plastic waste and carbon emissions, lignocellulosic residues, edible crop by-products, and algal biomass were utilized as sustainable raw materials. These biomasses provided carbohydrate-, lipid-, and lignin-rich fractions that were deconstructed through optimised physical, chemical, and enzymatic pretreatments to yield fermentable intermediates, such as reducing sugars, organic acids, and fatty acids. The intermediates were subsequently converted through tailored microbial fermentation processes into biopolymer precursors, primarily polyhydroxyalkanoates (PHAs) and lactate-based monomers. The resulting monomers underwent polymerization via polycondensation and ring-opening reactions to produce high-performance biodegradable plastics with tunable structural and mechanical properties. Additionally, the direct extraction and modification of naturally occurring polymers, such as starch, cellulose, and lignin, were explored to develop blended and functionalized bioplastic formulations. Comparative evaluation revealed that these biomass-derived polymers possess favourable physical strength, thermal stability, and biodegradability under composting conditions. Life-cycle evaluation further indicated a significant reduction in greenhouse gas emissions and improved carbon recycling compared to fossil-derived counterparts. The study demonstrates that integrating agricultural residues into bioplastic production not only enhances waste valorization and rural bioeconomy but also supports sustainable material innovation for packaging, farming, and consumer goods industries. These findings position agriculture-based biodegradable polymers as a critical component of circular bioeconomy strategies, contributing to reduced plastic pollution and improved environmental sustainability. Full article

Our Goal is to identify how colorectal cancer (CRC) arises in the single-layered cell epithelium (simple columnar epithelium) that lines the luminal surface of the large intestine. Background: We recently reported that the dynamic organization of cells in colonic epithelium is encoded by five biological rules and conjectured that colon tumorigenesis involves an autocatalytic tissue renewal reaction. Introduction Our objective was to define how altered crypt turnover explains tissue disorganization that leads to adenoma morphogenesis and CRC. Hypothesis: Changes in rate of tissue renewal-based cell polymerization leads to epithelial expansion and tissue disorganization during adenoma histogenesis. Methods: Accordingly, we created a computational model that considers the structure of colonic epithelium to be a polymer of cells and that tissue renewal is autocatalytic. Indeed, self-renewal of stem cells in colonic crypts continuously produces cells that act like monomers to form a polymer of cells (an interconnected, continuous cell sheet) in a polymerization-based process. Our model is a system of nonlinear differential equations that simulates changes in human crypt cell population dynamics. Results: We investigated how changes occur in the proportion of different cell types during adenoma development in FAP patients. The results show premalignant colonic crypts have a decreased rate of tissue renewal due to APC-mutation. Discussion: This slower rate of cell polymerization causes a rate-limiting step in the crypt renewal process that expands the proliferative cell population size. Conclusions: Our findings provide a mechanism that explains how a prolonged rate of crypt renewal leads to tissue disorganization with local epithelial expansion, infolding, and contortion during adenoma morphogenesis.: Full article

In this work, a complex and eco-friendly biomass raffinose monomer-modified polycarboxylate superplasticizer (RAF-PCE) was designed and synthesized via the free radical polymerization technique to simultaneously improve paste fluidity and delay fluidity loss in concrete applications. The adsorption, fluidity, and early hydration behaviors of cementitious systems after the introduction of RAF-PCE have been systematically investigated. Experimental results demonstrate that the hydroxy group in raffinose promotes the adsorption of RAF-PCE on the cement particles, thereby elevating the dispersion characteristic of cement paste through electrostatic repulsion, enabling excellent initial fluidity (310 mm). Additionally, its steric hindrance effect has also been identified to play a role in improving paste fluidity and reducing the slump loss of cement slurry. Detailed analyses unveil that RAF-PCE can reduce the concentration of free Ca²⁺ in the pore solution through complexation with Ca²⁺, which prevents the early precipitation of hydration products and realizes a delayed effect on cement hydration, ultimately evolving into a homogeneous and compact microstructure for superior compressive tensile strength of the cement mortar. The 28-day compressive strength of cement incorporating RAF-PCE reached 79.2 MPa, representing a 5.5% enhancement over conventional PCE systems. Our work provides novel insights into the promotion of innovative and green development in the concrete industry by utilizing renewable biomass resources for high-performance materials. Full article

The rapid accumulation of plastic and textile waste, particularly polyethylene terephthalate (PET), has emerged as a global challenge for sustainable resource management. Conventional recycling methods, including mechanical and chemical routes, recover limited value and often degrade material quality while consuming substantial energy. Biocatalytic recycling, by contrast, offers a resource-efficient alternative that transforms post-consumer PET into high-purity monomers under mild and environmentally benign conditions. This review examines advances in enzymatic PET depolymerization, focusing on hydrolases such as cutinases, PETases, MHETases, and lipases. The discussion highlights enzyme engineering, reactor design, and process integration that improve kinetics, thermostability, and yield. From a resource perspective, biocatalytic recycling redefines PET waste as a renewable carbon feedstock capable of re-entering industrial cycles, thereby reducing reliance on virgin petrochemicals and mitigating greenhouse gas emissions. Ultimately, this review positions biocatalytic PET recycling as a cornerstone technology for achieving circularity and advancing global resource sustainability. Full article

Styrene is an aromatic compound widely used as a reactive monomer in polyester resins, which are among the most utilized resins in cured-in-place pipe (CIPP) technology, the most widely used trenchless pipe renewal method. Given that styrene is classified as a suspected human carcinogen, this study aims to evaluate styrene concentrations emitted into the air during sewer pipe rehabilitation using CIPP. This study included developing a comprehensive methodology to collect data from six different CIPP installations across the U.S. and document styrene emissions before, during, and after the curing process. The air samples were collected and analyzed using the USEPA method TO-15 and TO-17. Measured styrene emissions were then compared with exposure limits established by USEPA, NIOSH, and OSHA to assess potential occupational and worker health impacts. The result confirmed that high styrene concentrations, exceeding the established threshold, can be observed within the CIPP work zone. The result also indicated a considerable reduction in styrene concentration within five feet downwind of the work zone. In conclusion, while the health risk to the public appears to be low, there is a potential for health impact for the CIPP crew. Therefore, implementing real-time air quality monitoring during CIPP installation to mitigate these health risks is recommended. Additionally, the use of appropriate personal protective equipment (PPE) by the crew is essential. Full article

The increasing demand for sustainable materials has propelled the development of bio-based elastomers derived from renewable terpenes. This study presents the synthesis of high-cis poly(butadiene-co-terpene) copolymers using coordination chain transfer polymerization with neodymium-based catalysts, enabling precise control of molecular weight and microstructure. Two terpene monomers, β-myrcene and trans-β-farnesene, were incorporated up to 45 wt% without compromising the elastomeric 1,4-cis polybutadiene segments. The copolymers were evaluated as impact modifiers in acrylonitrile–butadiene–styrene (ABS) and as vulcanizable rubber formulations. ABS containing bio-based copolymers exhibited distinct rubber morphologies, including elongated and rod-like particles with average particle diameters greater than 1042 nm and rubber phase volume fraction values ≥ 0.49, resulting in improved impact resistance exceeding 580 J/m and elongation at break higher than 12%. Vulcanized rubbers incorporating terpene segments displayed tunable curing kinetics, mechanical properties, and dynamic mechanical behavior, with notable increases in elongation (up to ~520%) and elasticity attributed to lower crosslink density (<1.20 × 10⁻⁴ mol/mL). Additionally, its energy dissipation capacity has been enhanced compared to the high-cis polybutadiene. These findings highlight the potential of terpene-derived bioelastomers as sustainable alternatives to fossil-based rubbers, offering comparable or enhanced performance for engineering polymer applications. The study underscores important structure–property relationships, providing a foundation for further optimization toward industrial adoption. Full article

This study investigates the surface properties of bio-based unsaturated polyester resin (b-UPR) nanocomposites reinforced with biosilica nanoparticles derived from rice husk. The b-UPR matrix was synthesized from recycled polyethylene terephthalate (PET) and renewable monomers, providing a sustainable alternative to conventional polyester resins. Unmodified and modified biosilica particles with silanes: (3-trimethoxysilylpropyl methacrylate—MEMO, trimethoxyvinylsilane—VYNIL, and 3-aminopropyltrimethoxysilane with biodiesel—AMBD) were incorporated in different amounts to evaluate their influence on the wettability, topography, and viscoelastic behavior of the composites. Contact angle measurements revealed that the addition of modified biosilica significantly improved the hydrophobicity of the b-UPR surface. The greatest increase in the wetting angle, amounting to 79.9% compared to composites with unmodified silica, was observed in the composites containing 5 wt.% SiO₂-AMBD. Atomic force microscopy (AFM) analysis indicated enhanced surface roughness and uniform dispersion of the nanoparticles. For the composite containing 1 wt.% of silica particles, the surface roughness increased by 25.5% with the AMBD modification and by 84.2% with the MEMO modification, compared to the unmodified system. Creep testing demonstrated that the reinforced nanocomposites exhibited improved dimensional stability under sustained load compared to the neat resin. These findings confirm that the integration of surface-modified biosilica not only enhances the mechanical properties but also optimizes the surface characteristics of bio-based polyester composites, broadening their potential for high-performance and sustainable applications. Full article