Sustainable Polymers Research Articles

Development and Evaluation of User‐Friendly Modeled Approach for Sustainable Polymer Membranes for Advanced Hemodialysis

AbstractHemodialysis is crucial for patients with end‐stage renal disease, yet evaluating its operating parameters often requires complex mathematical models. To simplify this process, user‐friendly modules have been developed to accurately assess key parameters with minimal inputs, enabling users to track disease prognosis. These modules incorporate governing equations and allow straightforward analysis. Validation against experimental data from polymer membrane studies demonstrated that at a blood flow rate of 300 mL min−1, the model predicted a clearance of 262 mL min−1, showing 7% difference from the actual value of 281 mL min−1. At a dialysate flow of 400 mL min−1, the model's predicted clearance was 286.47 mL min−1, with only a 1% difference compared to previous model. The module also showed 40% higher clearance in counter‐current flow compared to co‐current, with a 47% difference at 400 mL min−1 dialysate flow. Increasing the hollow fibre length from 27 to 50 cm led to a 4% clearance increase. Additionally, increasing residual renal clearance by 0.5 mL min−1 doubled the standard Kt V−1 Kt/V, and similar effects were seen by increasing weekly hemodialysis sessions. The app allows simulations, plots, and comparisons with minimal inputs and can be integrated into MATLAB or other platforms, benefiting both patients and researchers in prognosis and treatment analysis.

Enlightenment the dynamic behavior of norbornene–modified ’click’ 4–arm polyethylene glycol hydrogel: Delving into framework properties and transport properties through molecular dynamics simulations

The thiol-norbornene cross-linked 4-arm Polyethylene Glycol (PEG) ’click’ hydrogel is a synthetic, sustainable, and bio-inspired polymer extensively used in biomedical applications. Experimental techniques are widely used to study this system, whereas all-atom molecular dynamics simulations, which offer insight into the dynamic behaviours of the system, are never used to study this system. Three models of thiol-norbornene cross-linked PEG ’click’ hydrogel and a base PEG hydrogel are crafted. It is immersed in water to study its structural and transport properties. Structural properties are analysed through root-mean-square deviation (RMSD), radial distribution function (RDF), hydrogen bonds (H-bond), and stress–strain behavior. The RMSD reveals that the norbornene component enhances hydrogel stability compared to the base model. The RDF illustrates interactions between oxygen in PEG chains and water. H-bond results underscore PEG’s strong H-bond acceptance. The norbornene-functionalized crosslinked PEG hydrogel displays maximum H-bonding. It demonstrates a superior swelling ratio attributed to freezing and non-freezing water effects, indicating high stability and potential suitability for applications. Mean square displacements (MSD) unveil the diffusion coefficients of the hydrogel. The base hydrogel model shows the diffusive behavior, and the diffusion coefficient is 1.97 × 10-10 m2/s. The base model has the highest MSD value compared to other systems. The thiol-norbornene crosslinked click hydrogel has the highest Young’s modulus, which signifies the stiffness of the material. Findings illuminate thiol-norbornene ’click’ PEG hydrogel behaviour, emphasising chemical cross-linking’s crucial role in advanced biomedical applications.

Surface metamorphosis techniques for sustainable polymers: Optimizing material performance and environmental impact

The transition to sustainable polymers is crucial for reducing the environmental footprint of additive manufacturing, particularly in fused deposition modeling (FDM). This study investigates surface metamorphosis techniques—methods to modify polymer surfaces at micro and nanoscale levels to enhance performance and minimize environmental impact. We explore plasma treatment, chemical etching, and laser texturing on biodegradable and recycled polymers, assessing their effects on surface properties, such as adhesion, roughness, and chemical resistance. Our results demonstrate significant enhancements in mechanical properties. For example, PLA’s tensile strength increased from 55.3 MPa (untreated) to 63.8 MPa (plasma treated), and its elongation improved from 4.2% to 5.1%. PHA showed a similar trend, with tensile strength rising from 45.1 MPa to 52.6 MPa, and elongation increasing from 5.6% to 6.4%. rPET and rPP also exhibited improvements, indicating the effectiveness of these surface treatments. Employing a multi-criteria decision-making approach, we assess and prioritize these techniques based on their mechanical enhancements and sustainability profiles. While this study presents hypothetical results, it establishes a comprehensive framework for optimizing surface metamorphosis processes, guiding future experimental research. Our findings suggest that tailored surface modifications can significantly improve the performance and environmental sustainability of polymers in FDM, offering pathways for integrating eco-friendly materials into advanced manufacturing. This work contributes to the development of green manufacturing technologies by highlighting surface metamorphosis as a key strategy for achieving high-performance and sustainable materials.

Drying temperature effect on the characteristics of cationically polymerized kraft lignin

In this work, the effect of drying temperature (55–130 °C) on the properties of kraft lignin (KL) polymerized with [2-(methacryloyloxy)ethyl] trimethyl ammonium chloride, as a sustainable polymer (KLM) was investigated. KLM exhibited a 3-fold drop in charge density and a 10 % reduction in water solubility. These alterations were found to be associated with both chemical and physical changes determined by NMR and XPS analyses. At 55 °C, chain interactions were predominant due to electrostatic interactions amongst the pMETAC chains with the electronegative atoms present in KL. At 80, 105, and 130 °C drying temperatures, hydrolysis reactions predominated. The KLM polymer possessed, comparatively, a lesser resistance to thermal degradation than KL, and the KLM polymer had a more uniform thermal degradation behavior across the drying temperatures. Glass transition temperature, Tg, was shown to be comparable for KL across the various drying temperatures. KLM, however, showed an increasing trend as drying temperature increased, up to 130 °C, at which point Tg dropped due to KL degradation. Therefore, the drying temperature has a significant impact on the properties of kraft lignin and its cationic polymerized derivative, and it should be carefully selected to minimize the undesired changes in lignin properties.

Enhancing the Stereocomplex Crystallization of PLLA/PDLA Symmetric Blend by Controlling the Degree of Molecular Chain Entanglement

In order to enhance the content of stereocomplex crystals (SC) in poly L-lactic acid (PLLA)/poly D-lactic acid (PDLA) symmetric blend, thereby improving the defects of low crystallinity and poor heat resistance of polylactic acid (PLA)-based materials, the samples with different entanglement degrees were prepared by freezing extration method. The critical overlap concentration of the blend system was quantitatively obtained using an Ubbelohde viscometer. Based on this concentration, samples with a series of concentration gradient were prepared to control the different degrees of molecular chain entanglement inside. The results indicated that the chain disentanglement could greatly increase the content of SC in the blend, whether in the precipitation crystallization or the melt crystallization process. Especially after the isothermal crystallization for 30min at 130oC, the L/D-0.1 sample with the highest degree of disentanglement almost only formed SC, accounting for 95.2% of the total crystallinity. Samples with lower entanglement degree had more crystal nuclei and faster growth rate of formed spherulites. For completely entangled sample L/D-50, the crystal nucleus of homo-crystalls (HC) could be considered as SC. Besides, the Vicat softening temperature (VST) of L/D-0.1 sample increased from 79.9oC of L/D-50 sample to 103.8oC with an obvious increase of 24.9oC. All these results provide new ideas for improving the performance of PLA-based materials and show promising development prospects of green and sustainable polymers.

Hole drilling in basalt-reinforced sustainable composites using abrasive waterjet for construction applications

This study aimed to develop, characterize, and optimize abrasive waterjet (AWJ) machining of sustainable basalt fiber-reinforced polymer composites for construction and industrial applications. Dynamic mechanical analysis, thermogravimetric analysis, and X-ray diffraction revealed enhanced thermal stability, increased decomposition temperatures, and improved crystallinity, correlating with improved tensile strength of developed composites. To address drilling-induced damage that can compromise long-term quality and applicability, AWJ drilling parameters were optimized to minimize damage while enhancing material removal rates. A novel quantification method for entry total surface damage (ETD) was implemented to assess machining defects. Results showed that standoff distance significantly influences ETD and exit delamination, while higher water pressure reduces entry damage. Abrasive flow rate primarily affected the material removal rate. FE-SEM analysis revealed microstructural changes in drilled surfaces, including damage zones and matrix fractures specific to AWJ processing. Multi-objective optimization using Genetic Algorithm is performed to enable flexible parameter selection and informed decision making, balancing machining efficiency and minimal damage.

Sulfur-containing cellulose esters for selectively anchoring gold for water catalytic decontamination

The facile preparation of sustainable sulfur-containing polymer functional materials has been obtained great attention due to their chemical reactivity and metal complexing ability. In this study, taking the solution properties advantages of the newly developed cellulose solvent system of DBU/DMSO/CO2, thiol and disulfide bond functionalized cellulose ester (TDSCE) was facilely prepared via in-situ tandem transesterification and oxidation reaction by using methyl 3-mercaptopropionate, without adding any external catalyst. The synthetic protocol was featured by that the DBU not only acted as reagent for the dissolution of cellulose, but also catalysts for the transesterification of cellulose with methyl 3-mercaptopropionate to yield cellulose 3-mercaptopropionate (Cell-MP) with maximum degrees of substitution (DS) of 0.77, and an oxidant for the partial oxidation of Cell-MP to produce a cellulose methyl 3,3′-disulfanediyldipropionate (Cell-MDSP) with maximum DS of 0.36 mixed ester, respectively. With successful introduction of thiol and disulfide bond into the cellulose backbone, the TDSCEs indicated desirable selective absorption of Au3+ from mimic heavy mental ions waste water due to the sulfur-Au chemistry with maximal adsorption capacity for Au3+ of 415.2 mg/g. The subsequent reduction of Au3+ into gold nanoparticles (Au NPs) fabricated a robust TDSCE-2@Au NPs composite catalyst with high catalytic activity for the hydrogenation treatment of water pollutes, such as 4-nitrophenol (4-NP)and azo dyes.

Recent Advance of Sustainable Polymers for Packaging Applications

The extensive application of non-renewable polymers has brought about deep environmental concerns, demonstrating the immediate requirement for new biodegradable and biobased packaging choices. The work offers an in-depth look at a wide array of degradable and biobased polymers like Polylactic Acid (PLA), Polyhydroxyalkanoates (PHA), and Polyvinyl Alcohol (PVOH), as well as starch and cellulose materials, discussing their qualities, uses, and the issues faced in food packaging. These types of green polymers, either in new ways or from renewable sources, offer great advances not only from decomposition into harmless parts but also from the reduction of environmental damage. The essay covers the exploitation side of this material, be it the role of PLA in enzymatic, hydrolytic, or microbial degradations, or the main tactical function of PHA in terms of a water barrier aimed at preserving the quality of stored food. Additionally, the multifunctionality of these substances is represented anew in packaging dairy goods, such as fruits, and vegetables, and specialized applications like edible films or water-soluble bags. The participation of compostable polymers has become increasingly vital in the area of food packaging to meet consumers’ demands and to upgrade the present science technologies aimed at guiding food producers who are looking for more sustainability in their business.

Thinking Green on 3D Printing: Sustainable Polymer Compositions of Post-Consumer Polypropylene and Tire Rubber Crumbs Intended for Industrial Applications.

Year by year, more and more plastic is used worldwide. A large part of post-consumer waste is still stored in landfills instead of being reused. The solution to this problem may be recycled materials (recyclates) or biodegradable materials. The method of 3D printing, regarded as a clean processing technology, can significantly contribute to addressing global plastic pollution by utilizing post-consumer recycled polymers to create new components and parts. Therefore, this study focuses on the assessment of various properties and characteristics of 3D-printed compositions based on post-consumer polypropylene (PP) and rubber crumbs, recycled from packages foils and car tires, respectively. Moreover, within this study, we compared the mechanical performance of the injection molding material with the one obtained from 3D printing. A characterization was made considering the thermal and mechanical properties as well as the "print quality" through the microscopic and tomographic analysis of subsequent print passes, the number of free spaces, and imperfections in the polymer melt. Samples obtained using the FDM and injection methods exhibited comparable melting temperatures, while the samples obtained by injection molding exhibited slightly better mechanical performance, higher hardness, and impact strength.

Mechanical, thermal, and water absorption properties of HDPE/barley straw composites incorporating waste rubber

This study investigates the mechanical, thermal, and water absorption properties of high-density polyethylene (HDPE) composites filled with barley straw and varying amounts of waste rubber. The research aims to develop sustainable materials that repurpose agricultural and industrial waste while addressing resource scarcity and waste management challenges. Composites were prepared using a twin-rotor mixer and hydraulic press, with waste rubber content varying from 0 to 20 wt%. Mechanical properties were evaluated through tensile testing, thermal behavior was analyzed using TGA, DTG, and DSC, and long-term water absorption was measured. Results show that increasing waste rubber content from 0 to 20% led to a decrease in tensile strength (11.3 to 8.9 MPa) and tensile modulus (1760 to 790 MPa), while relative extension increased (2.4–5.9%). Thermal analysis revealed a slight reduction in onset degradation temperature (270 °C to 240 °C) and increased char residue (8–18%) with higher rubber content. Water absorption decreased significantly, from 12 to 13% to 6–7% after 600 h of immersion, as waste rubber content increased. These findings demonstrate that incorporating waste rubber into HDPE/barley straw composites results in materials with enhanced flexibility and water resistance at the cost of some strength and stiffness. In conclusion, the results of this study offer a clear pathway for the development of sustainable polymer composites that have broad potential applications across industries like construction, marine infrastructure, automotive, and packaging. By replacing traditional, resource-intensive materials with eco-friendly alternatives, these composites not only provide functional benefits but also support global efforts toward sustainable development and environmental conservation.

Melt Polycondensation Strategy to Access Unexplored l-Amino Acid and Sugar Copolymers.

Biodegradable polymers from bioresources are highly in demand for the development of sustainable polymer platforms for commodity plastics and in the biomedical field. Here, an elegant one-pot synthetic strategy is developed, for the first time, to access unexplored hybrid polymers from two naturally abundant resources: carbohydrates (sugars) and l-amino acids. A bottleneck in the synthetic strategy is overcome by tailor-making d-mannitol-based six- and five-membered bicyclic acetalized diols, and their structures are confirmed by single-crystal X-ray diffraction and 2D NMR spectroscopy. l-Amino acids are converted into ester-urethane functional monomers, and they are polymerized with sugar-diols under solvent-free melt polycondensation to yield biodegradable poly(ester-urethane)s. Acid-catalyzed deprotection yielded amphiphilic polymers having exclusively alternating residues of sugar and l-amino acid in the polymer backbone. The polymer is self-assembled into 200 ± 10 nm sized nanoparticles that can encapsulate fluorescent dyes, are nontoxic to cells up to 250 μg/mL, and are readily endocytosed for lysosomal enzymatic biodegradation at the cellular level.

Energy-efficient FDM printing of sustainable polymers: Optimization strategies for material and process performance

The integration of sustainable polymers in fused deposition modeling (FDM) 3D printing offers a promising pathway toward reducing the environmental impact of additive manufacturing. However, the energy-intensive nature of FDM processes presents a significant challenge to the overall sustainability of this technology. In this study, we explore the use of bio-based and recycled polymers in FDM printing and develop optimization strategies to reduce energy consumption without compromising material and print performance. Our results demonstrate that by systematically optimizing key printing parameters such as extrusion temperature, print speed, and layer height it is possible to achieve up to 20% energy savings. Additionally, we find that novel material formulations and advanced thermal management techniques enhance the mechanical properties of printed objects by up to 15%, all while minimizing energy use. This research not only advances the field of sustainable 3D printing but also provides a framework for the development of next-generation materials and processes that align with the principles of a circular economy.

Poly(butylene succinate) Microparticles Prepared Through Green Suspension Polycondensations

AbstractThe demand for sustainable polymer particles production is growing, driven by the need for efficient, biocompatible, and biodegradable materials. In this context, the present study explores the production of poly(butylene succinate) (PBS) particles in a single step using a green heterogeneous suspension process, using vegetable oil as the suspending medium. Particularly, the effects of oil type (soybean, corn, sunflower), dispersed phase holdup (10–30 wt.%), stabilizers (Span 20, Span 80, Tween 80, Brij 52, Brij 93, Igepal‐co‐520, Polyglycerol polyricinoleate (PGPR)), reaction time (1–5 h), and temperature (100–160 °C) on the suspension polymerization are investigated. Results indicate that particle size and shape are influenced by the vegetable oil and stabilizer. Additionally, it is shown that the particle size distribution is affected by the use of a sonicator, allowing the manufacture of even smaller microsized particles. Based on the results, a 30 wt.% holdup in corn oil with a blend of surfactants can be recommended, producing spherical particles with an average diameter of 100 µm. Moreover, higher reaction temperatures (160 °C) and longer reaction times (5 h) positively impacted the molar mass of the obtained particles. Finally, cytotoxicity tests using Bone Marrow‐Derived Macrophages cells confirmed the safe use of PBS microparticles at concentrations up to 1000 µg mL⁻¹

Microbial Enzymes for the Biodegradation of Polylactic Acid (PLA): Molecular Docking Simulation and Biodegradation Pathway Proposal

Polylactic acid (PLA), as a biodegradable polymer, finds widespread utility across diverse sectors, encompassing transportation, agriculture, biomedicine, textiles, electronics, and food packaging. Nonetheless, its degradation kinetics exhibit significant environmental sensitivity, necessitating the development of novel biotechnological methodologies to investigate the microbial and enzymatic constituents implicated in PLA biodegradation. In this review, molecular docking simulations are discussed to analyze the enzymatic degradation of PLA using specific enzymes: proteinase K, PLA depolymerase, and lipase. The binding energy, binding affinity, and dimensions of PLA-binding sites within the enzyme cavities have been examined for each enzyme. The binding amino acid residues mainly include serine, histidine, and aspartate for all plastics, while the interactions involve Van der Waals forces, conventional hydrogen bonding, carbon-hydrogen bonding, and Pi-interactions. Based on our synthesis of the literature, a theoretical PLA biodegradation pathway that illustrates the interaction pattern between PLA and the enzymes, as well as the degradation mechanism is proposed. Our review indicates that in natural environments, enzymes work synergistically, utilizing their unique properties to facilitate an efficient sequential catalytic process for PLA degradation. This integrative approach elucidates the mechanistic underpinnings and metabolic cascades governing PLA degradation, enriching insights into enzymatic catalysis and microbial enzyme-mediated plastic biotransformation. Consequently, a comprehensive understanding of these processes is paramount in optimizing biodegradation kinetics and enhancing the environmental performance of biodegradable polymers. This review provides a detailed framework for refining PLA management strategies and advancing sustainable polymer utilization.

Bio-derived epoxy thermosets incorporating imine linkages: Towards sustainable and advanced polymer materials

In the search for sustainable and eco-friendly alternatives, Schiff-based epoxy thermosets are emerging as a promising strategy due to the inherent dynamic and reversible nature of their imine functional groups, which enables thermal reprocessability and chemical recyclability. This article explores the synthesis of Schiff-based epoxy thermosets using sustainable approaches. Starting from vanillin or syringaldehyde, the synthesis involves the incorporation of imine linkages into the epoxy network. A new strategy has been employed by self-polymerization without the use of additional curing agents. This approach conducts to novel thermosets with superior material properties that exceed those reported in previous studies. Thermo-mechanical investigations showed that the designed thermosets have high mechanical properties, with storage moduli at room temperature ranging between 1.5–2.2 GPa, and glass transition values between 138 and 249 °C. Thermal analyses allowed to evaluate the Limit Oxygen Index (LOI) which ranged from 33 % to 36 %, demonstrating excellent flame-retardant properties without the addition of supplementary additives. Their reduced density (0.74–1.09 g/cm3) makes them suitable for applications where weight considerations are critical. These results obtained results place the designed Schiff-based materials as promising candidates for a wide range of high-end applications, particularly in industries that prioritize eco-friendly processes and materials.

Water-Enhancing Gels Exhibiting Heat-Activated Formation of Silica Aerogels for Protection of Critical Infrastructure During Catastrophic Wildfire.

A promising strategy to address the pressing challenges with wildfire, particularly in the wildland-urban interface (WUI), involves developing new approaches for preventing and controlling wildfire within wildlands. Among sprayable fire-retardant materials, water-enhancing gels have emerged as exceptionally effective for protecting civil infrastructure. They possess favorable wetting and viscoelastic properties that reduce the likelihood of ignition, maintaining strong adherence to a wide array of surfaces after application. Although current water-enhancing hydrogels effectively maintain surface wetness by creating a barricade, they rapidly desiccate and lose efficacy under high heat and wind typical of wildfire conditions. To address this limitation, unique biomimetic hydrogel materials from sustainable cellulosic polymers crosslinked by colloidal silica particles are developed that exhibit ideal viscoelastic properties and facile manufacturing. Under heat activation, the hydrogel transitions into a highly porous and thermally insulative silica aerogel coating in situ, providing a robust protective layer against ignition of substrates, even when the hydrogel fire suppressant becomes completely desiccated. By confirming the mechanical properties, substrate adherence, and enhanced substrate protection against fire, these heat-activatable biomimetic hydrogels emerge as promising candidates for next-generation water-enhancing fire suppressants. These advancements have the potential to dramatically improve the ability to protect homes and critical infrastructure during wildfire.

Catalytic oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid using Co-N/C catalysts with stepwise base addition approach

The production of 2,5-furandicarboxylic acid (FDCA) through green reaction routes is of crucial scientific value for the production of sustainable polymers. This study explores the active centers in cobalt-nitrogen-doped carbon (Co-N/C) for FDCA production. It was established that Co-Nx synergistically along with the nitrogen-doped carbon acted as centers for 5-hydroxymethylfurfural (HMF) oxidation. This study demonstrates a sustainable method for FDCA production from HMF without using precious metals, organic solvents, and harsh basic environments. Co-N/C catalyst displayed a high FDCA yield of ∼90% in an aqueous medium under mildly basic conditions in 34 h with 100% HMF conversion. An innovative strategy of stepwise base addition has been proposed to effectively accelerate the generation reaction of FDCA. The detrimental effects of high heating rate and calcination temperature on the active centers were also thoroughly investigated. Through DFT simulations it was established that Co-Nx aided in the activation of oxygen for HMF oxidation.

Emerging Trends in Engineering Polymers: A Paradigm Shift in Material Engineering

Emerging Trends in Engineering Polymers signify a pivotal transformation in material engineering, marking a departure from traditional materials towards innovative, multifunctional, and sustainable polymers. This review delineates the forefront of advancements in polymer materials, including high-performance, bio-based, biodegradable, innovative, and functional polymers. Highlighting their enhanced mechanical properties, thermal stability, and chemical resistance showcases these materials' pivotal role in driving technological progress. The exploration extends to advanced manufacturing techniques such as 3D printing, electrospinning, and the fabrication of polymer nanocomposites, underscoring their impact on customizing product properties and scaling production. Central to this discourse is the sustainability and environmental stewardship in the polymer sector, addressing recycling methodologies, the circular economy, and regulatory frameworks guiding sustainable practices. The review juxtaposes traditional and emerging recycling processes, illuminating the path toward more sustainable material cycles. Furthermore, it ventures into emerging applications across diverse sectors such as energy, electronics, healthcare, automotive, and aerospace, elucidating the transformative potential of engineering polymers in these domains. Challenges spanning technical, economic, environmental, and regulatory landscapes are critically examined, setting the stage for future directions in research and development. The review culminates in a forward-looking perspective, advocating for interdisciplinary collaboration and material science innovation to navigate modern engineering challenges' complexities. Through this comprehensive analysis, the review articulates a narrative of evolution and opportunity within engineering polymers, poised to redefine material engineering in the decades to come.

N-doped carbon nanospheres synthesized from a newly designed eco-friendly sustainable polymer for highly selective CO2 capture.

N-doped carbon nanospheres and porous carbon were produced by a hydrothermal template and the activation of hexamethylenetetramine (HMTA as a nitrogen source and activator) and ZnCl2 (only as an activator) from a poly(Ri-S-ε-CL-PDMS) multiblock/graft copolymer produced using a renewable resource and eco-friendly autoxidation. N-doped carbon nanospheres (PPiSiHMTA) exhibited excellent CO2 adsorption (2.73mmol/g at 0°C and 0.15atm, 1.72mmol/g at 25°C and 0.15atm) and CO2/N2 selectivity (344-512). Despite the higher BET surface area and pore volume, porous carbon (PPiSi) showed low CO2 adsorption (1.21 and 0.71mmol/g, 0.15atm) and CO2/N2 selectivity (57 and 112). PPiSiHMTA and PPiSi have low isosteric heats of adsorption (Qst, 18-33kJ/mol) and stability in humid environments. In addition, PPiSiHMTA exhibited an excellent CO2 recycling performance. The experimental data on CO₂ adsorption was evaluated using various isotherm models, including Freundlich, Langmuir, Sips, and Temkin. The results demonstrated a nearly perfect fit between the Freundlich isotherm and the experimental data, indicating the heterogeneous nature of the adsorbent surfaces. Our study is promising for industrial applications, offering excellent CO2 adsorption, CO2/N2 selectivity, moisture stability, and porous material fabrication strategies.

PREPARATION AND CHARACTERIZATION OF POLYMER INCLUSION MEMBRANES BASED ON BIODEGRADABLE CELLULOSE/ALGERIAN CLAY FOR HEAVY METALS REMOVAL FROM WASTEWATER

Separation membranes have gained attention as promising options for water and wastewater treatment due to their financial sustainability, and eco-friendliness. However, practical challenges have limited their application in water separation. To overcome these limitations, inorganic-organic hybrid membranes have been developed in this study. The present work deals with two attractive aspects: (i) economical, through the valorization of a local clay (Algerian kaolin), and (ii) environmental, which is based on the membrane selectivity for metal ions. The principal objective of this work is the development of enhanced nanocomposite membranes. It is achieved with low costs, based on cellulose triacetate (CTA) as a polymeric matrix modified by the addition of a lamellar filler, i.e. yellow clay obtained from Jijel, located in the east of Algeria, and plasticized by dioctyl phthalate (DOP). A further objective of this paper was the treatment of wastewater polluted by lead (Pb2+) and cadmium (Cd2+). The prepared membranes were characterized by various characterization techniques, including scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy and thermogravimetric analysis (TGA). All synthetized membranes had an amorphous structure, with homogeneous pore morphology and distribution. Moreover, the presence of nanocomposite clay showed effective integration into the membrane matrix and led to a significant improvement in thermal resistance. These membranes were applied to treat a synthetic aqueous solution contaminated with heavy metals, namely Pb2+ and Cd2+. The results revealed a rejection rate higher than 50%, suggesting the potential effectiveness of a stable and environmentally sustainable polymer inclusion membrane system for water purification.