Search Results (533)

Biodegradable polymers offer environmental advantages compared to fossil-based alternatives, but they currently lack the stretchability required for demanding applications such as mesh fabrics for woven flexible intermediate bulk container (FIBC) bags and stretch, shrink, and cling films. The goal of this research is to enhance the stretchability of biodegradable blends based on 80% poly(butylene adipate-co-terephthalate) (PBAT) and 20% poly(lactic acid) (PLA) through reactive extrusion. Radical initiator (dicumyl peroxide (DCP)) and chain extenders (maleic anhydride (MA), glycidyl methacrylate (GMA)) were employed to improve the melt strength and elasticity of the extruded films. The reactive blends were initially prepared using a batch mixer and subsequently compounded in a twin-screw extruder. Films were produced via cast extrusion. 0.1% wt. DCP led to a 200% increase in elongation at break and a 44% improvement in tensile strength. Differential scanning calorimetry and scanning electron microscopy revealed enhanced miscibility between components. Shear and complex viscosity increased by 38% and 85%, compared to the neat blend, respectively. Reactive extrusion led to a better dispersion and distribution of the phases. An improved interfacial adhesion between the phases, in addition to higher molecular weight, led to enhanced melt strength and improved stretchability. Full article

Against the backdrop of global energy transition and strict environmental regulations, supercritical carbon dioxide (scCO₂) fracturing and oil displacement technologies have emerged as pivotal green approaches in shale gas exploitation, offering the dual advantages of zero water consumption and carbon sequestration. However, the inherent low viscosity of scCO₂ severely restricts its sand-carrying capacity, fracture propagation efficiency, and oil recovery rate, necessitating the urgent development of high-performance thickeners. The current research on scCO₂ thickeners faces a critical trade-off: traditional fluorinated polymers exhibit excellent philicity CO₂, but suffer from high costs and environmental hazards, while non-fluorinated systems often struggle to balance solubility and thickening performance. The development of new thickeners primarily involves two directions. On one hand, efforts focus on modifying non-fluorinated polymers, driven by environmental protection needs—traditional fluorinated thickeners may cause environmental pollution, and improving non-fluorinated polymers can maintain good thickening performance while reducing environmental impacts. On the other hand, there is a commitment to developing non-noble metal-catalyzed siloxane modification and synthesis processes, aiming to enhance the technical and economic feasibility of scCO₂ thickeners. Compared with noble metal catalysts like platinum, non-noble metal catalysts can reduce production costs, making the synthesis process more economically viable for large-scale industrial applications. These studies are crucial for promoting the practical application of scCO₂ technology in unconventional oil and gas development, including improving fracturing efficiency and oil displacement efficiency, and providing new technical support for the sustainable development of the energy industry. This study innovatively designed an amphiphilic modified amino silicone oil polymer (MA-co-MPEGA-AS) by combining maleic anhydride (MA), methoxy polyethylene glycol acrylate (MPEGA), and amino silicone oil (AS) through a molecular bridge strategy. The synthesis process involved three key steps: radical polymerization of MA and MPEGA, amidation with AS, and in situ network formation. Fourier transform infrared spectroscopy (FT-IR) confirmed the successful introduction of ether-based CO₂-philic groups. Rheological tests conducted under scCO₂ conditions demonstrated a 114-fold increase in viscosity for MA-co-MPEGA-AS. Mechanistic studies revealed that the ether oxygen atoms (Lewis base) in MPEGA formed dipole–quadrupole interactions with CO₂ (Lewis acid), enhancing solubility by 47%. Simultaneously, the self-assembly of siloxane chains into a three-dimensional network suppressed interlayer sliding in scCO₂ and maintained over 90% viscosity retention at 80 °C. This fluorine-free design eliminates the need for platinum-based catalysts and reduces production costs compared to fluorinated polymers. The hierarchical interactions (coordination bonds and hydrogen bonds) within the system provide a novel synthetic paradigm for scCO₂ thickeners. This research lays the foundation for green CO₂-based energy extraction technologies. Full article

To broaden clean asphalt modification methods, this study employs a composite polymer of maleic anhydride-grafted styrene-butadiene-styrene (MA-g-SBS) and styrene-butadiene-styrene (SBS) as a modifier. The composite is formulated into polymer latex and used to modify emulsified asphalt. Routine performance tests were conducted on MA-g-SBS/SBS composite latex-modified emulsified asphalt (MSMEA) with varying ratios to determine the optimal composition. The ideal ratio was found to be MA-g-SBS:SBS = 1:4. Subsequently, conventional property tests, rheological analyses, microphase structure observations, and bending beam creep tests were conducted on MSMEA with the optimal ratio to assess the impact of the composite latex on asphalt performance. Findings indicated that increasing the latex content significantly enhanced the softening point and ductility while reducing penetration. These macroscopic improvements were notably superior to those achieved with single SBS latex modification. Fluorescence microscopy revealed that at low dosages, the MA-g-SBS/SBS composite dispersed uniformly as point-like structures within the asphalt. At higher dosages (above 5%), a distinct network structure emerged. The addition of the composite latex raised the complex shear modulus and rutting factor while reducing the phase angle, with pronounced fluctuations observed between 4% and 5% dosages. This suggests a substantial enhancement in the high-temperature performance of the emulsified asphalt, attributed to the formation of the network structure. FT-IR results confirmed that a chemical reaction occurred during the modification process. Additionally, the bending beam creep test demonstrated that the composite latex reduced asphalt brittleness and improved its low-temperature performance. Full article

This study presents the development of a sustainable composite material by incorporating by-products from the cork industry into acrylonitrile butadiene styrene (ABS), with the aim of reducing the environmental impact of plastic composites while maintaining their performance. ABS, a petroleum-based polymer, was used as the matrix, and maleic anhydride (MAH) with dicumyl peroxide (DCP) served as a compatibilizing system to improve interfacial adhesion with cork microparticles. Composites were prepared with 10% w/w cork in various particle sizes and characterized via FTIR, X-ray computed tomography, SEM, mechanical testing, and thermal analysis. The best performing formulation (CPC-125) showed a reduction of only ~16% in tensile modulus and ~7% in tensile strength compared with ABS-g-MAH, with a more pronounced decrease in strain at break (3.23% vs. 17.47%) due to the cork’s inherent rigidity. Thermogravimetric and calorimetric analysis confirmed that thermal stability and processing temperatures remained largely unaffected. These results demonstrate the feasibility of incorporating cork microparticles as a bio-based reinforcing filler in ABS composites, offering a promising strategy to reduce the use of virgin plastics in applications compatible with conventional injection molding. Full article

Chemical control is key to minimizing agricultural losses, driving the search for more efficient and selective herbicides. This study reports the synthesis of epoxyoxirenes, their phytotoxic evaluation, and an in silico analysis to identify the protein target of the most active compound in plants. Compounds 2–19 were tested on Lactuca sativa spp., Allium cepa spp., Cucumis sativus spp., Triticum aestivum, and Bidens pilosa. The synthetic route began with anhydride 1, obtained via a Diels–Alder reaction between maleic anhydride and furan (91% yield). Anhydride 1 was converted into amides 2–7 through reactions with aromatic amines (>92% yields), followed by cyclization to imides 8–13 (60–83% yields), and subsequent epoxidation to afford epoxides 14–19 (62–98% yields). All the compounds interfered with seedling development, with compounds 2–7 showing the greatest phytotoxicity to B. pilosa at concentrations of 500 μM and 1000 μM. An in silico analysis suggested plant tubulin as a potential protein target for the most active compounds. These findings highlight epoxyoxirenes as promising scaffolds for novel herbicide development and support further investigation into their mechanism of action. Full article

A novel and general approach to the practical ROMP polymerization of cinchona alkaloid derivatives providing novel hybrid materials having quinine attached on a poly(norbornene-5,6-dicarboxyimide) matrix is presented. The concept involves an easy modification of quinine (in general, any cinchona alkaloid) toward clickable 9-azide that reacts with N-propargyl-cis-5-norbornene-exo-2,3-dicarboxylic imide in Cu(I)-catalyzed Huisgen cycloaddition (click chemistry). The resulting monomers undergo a controllable ROMP reaction that leads to novel polymers of a desired length and solubility. This sequence allows for the facile preparation of a regularly decorated polymeric material having one quinine moiety per single mer of the polymer chain inaccessible using typical immobilization methods. A poly(norbornene-5,6-dicarboxyimide) type of polymeric matrix was selected due to the high reactivity of the exo-norbornene motif in Ru(II)-catalyzed ROMP and its chemical and thermal stability as well as convenient, scalable access from inexpensive cis-5-norbornene-exo-2,3-dicarboxylic anhydride (‘one-pot’ Diels–Alder reaction of dicyclopentadiene and maleic anhydride). An appropriate combination of a Grubbs catalyst, Ru(II) (G1, G2), and ROMP conditions allowed for the efficient synthesis of well-defined soluble polymers with mass parameters in the range Mn = 2.24 × 10⁴ – 2.26 × 10⁴ g/mol and Mw = 2.90 × 10⁴–3.05 × 10⁴ g/mol with good polydispersity, Đ_M = 1.32–1.35, and excellent thermal stability (up to 309°C T_d10). Spectroscopic studies (NMR and electronic circular dichroism (ECD)) of these products revealed a linear structure with the slight advantage of a trans-configuration of an olefinic double bond. The resulting short-chain polymer discriminates mandelic acid enantiomers with a preference for the (R)-stereoisomer in spectrofluorimetric assays. This concept seems to be rather general with respect to other molecules dedicated to incorporation into the poly(norbornene-5,6-dicarboxyimide) chain. Full article

This study aims to improve the performance of wood–plastic composites (WPCs) composed of cotton stalk powder and residual film particles. Additionally, it aims to promote the efficient utilization of cotton stalk biochar. The composites were prepared using modified cotton stalk biochar and xylem powder as the matrix, maleic anhydride grafted high-density polyethylene (MA-HDPE) as the coupling agent, and polyethylene (PE) residual film particles as the filler. The WPCs were fabricated through melt blending using a twin-screw extruder. Mechanical properties were evaluated using a universal testing machine and texture analyzer, Shore D hardness was measured using a durometer, and microstructure was analyzed using a high-resolution digital optical microscope. A systematic investigation was conducted on the effect of biochar content on material properties. The results indicated that modified biochar significantly enhanced the mechanical and thermal properties of the WPCs. At a biochar content of 80%, the material achieved optimal performance, with a hardness of 57.625 HD, a bending strength of 463.159 MPa, and a tensile strength of 13.288 MPa. Additionally, thermal conductivity and thermal diffusivity decreased to 0.174 W/(m·K) and 0.220 mm²/s, respectively, indicating improved thermal insulation properties. This research provides a novel approach for the high-value utilization of cotton stalks and residual films, offering a potential solution to reduce agricultural waste pollution in Xinjiang and contributing to the development of low-cost and high-performance WPCs with wide-ranging applications. Full article

In this study, a flame-retardant wood-polymer composite was produced using huntite-hydromagnesite mineral, recognized for its non- flammability properties. In this context, wood-polymer composites were produced with the co-rotating twin-screw extrusion technique, while polypropylene was applied as the composite matrix, medium density fiberboard waste and inorganic huntite-hydromagnesite mineral were used as the reinforcement material. The proportion of wood powder additives was changed to 10% and 20%, and the huntite and hydromagnesite ratio was changed to 30%, 40%, 50% and 60%. Maleic anhydride grafted polypropylene, i.e., MAPP, was applied as a binder at a rate of 3%. Polypropylene, wood fibers, mineral powders, and MAPP blended in the mixer were processed in the extruder and turned into granules. Structural, morphological, thermal, mechanical, and flame-retardant properties of the composites were analyzed using XRD, SEM, FTIR, TGA, tensile testing, and the UL-94 vertical flammability test. Test samples were prepared to evaluate the physical and mechanical properties with a compression molding machine. It was concluded that the composites gained significant flame retardancy with the addition of huntite hydromagnesite. The potential for using this material in various fields and its compliance with the principles of circular economy and the Sustainable Development Goals (SDG 12) were noted. Full article

The development of eco-friendly surfactants is pivotal for enhanced oil recovery (EOR). In this study, a novel lignin-derived zwitterionic surfactant (DMS) was synthesized through a two-step chemical process involving esterification and free radical polymerization, utilizing renewable alkali lignin, maleic anhydride, dimethylamino propyl methacrylamide (DMAPMA), and sulfobetaine methacrylate (SBMA) as precursors. Comprehensive characterization via ¹H NMR, FTIR, and XPS validated the successful integration of amphiphilic functionalities. Hydrophilic–lipophilic balance (HLB) analysis showed a strong tendency to form stable oil-in-water (O/W) emulsions. The experimental results showed a remarkable 91.6% viscosity reduction in Xinjiang heavy crude oil emulsions at an optimum dosage of 1000 mg/L. Notably, DMS retained an 84.8% viscosity reduction efficiency under hypersaline conditions (total dissolved solids, TDS = 200,460 mg/L), demonstrating exceptional salt tolerance. Mechanistic insights derived from zeta potential measurements and molecular dynamics simulations revealed dual functionalities: interfacial modification by DMS-induced O/W phase inversion and electrostatic repulsion (zeta potential: −30.89 mV) stabilized the emulsion while disrupting π–π interactions between asphaltenes and resins, thereby mitigating macromolecular aggregation in the oil phase. As a green, bio-based viscosity suppressor, DMS exhibits significant potential for heavy oil recovery in high-salinity reservoirs, addressing the persistent challenge of salinity-induced inefficacy in conventional chemical solutions and offering a sustainable pathway for enhanced oil recovery. Full article

This study investigates the mechanical, thermal, and liquid resistance properties of injection-molded composites made from recycled polypropylene (rPP) reinforced with jute fillers. Maleic anhydride-grafted polypropylene (MAPP) was used as a compatibilizer to enhance filler–matrix interfacial bonding. Tensile, flexural, and Charpy impact tests, along with density measurements, heat deflection temperature (HDT) tests, and resistance to short-duration liquid contact, were conducted to evaluate the composites. Results indicate that the addition of jute powder significantly improved stiffness (Young’s modulus increased up to 233%) and thermal stability (HDT increased to 147 °C for rPP/J40/MAPP) while reducing impact toughness due to the brittle nature of jute fillers. MAPP-modified composites demonstrated enhanced tensile and flexural strength compared to unmodified counterparts, with tensile strength improving by approximately 23% for rPP/J30/MAPP. The composites exhibited excellent liquid resistance, showing no visible changes after exposure to various automotive and household fluids. Full article

The photosensitive properties of smart photoactive polymers give them a wide range of potential applications across various fields. This study focuses on designing polymeric systems that incorporate hydrophilic polymers, with the primary goal of adapting these materials for biological applications. Specifically, it aims to contribute to the development of photochromic materials for optical processing, utilizing both molecular and macromolecular components. Additionally, this study evaluates the effectiveness of photoactive polymers in photodynamic therapy (PDT). It details the synthesis and characterization of photoactive copolymers derived from maleic anhydride (MAn) combined with vinyl monomers such as 2-methyl-2-butene (MB) and 1-octadecene (OD), as well as the organic compound 1-(2-hydroxyethyl)-3,3-dimethylindoline-6-nitrobenzopyran (SP). The two novel optically active alternating polymeric systems, poly(maleic anhydride-alt-octadecene) and poly(maleic anhydride-alt-2-methyl-2-butene), were functionalized with SP through an esterification process in a 1:1 monomer feed ratio, using pyridine as a catalyst. This methodology incorporated approximately 100% of the photoactive molecules into the main acrylic chain to prepare the alternating copolymers. These copolymers were characterized by UV-visible, FTIR, and 1H-NMR spectroscopy and analysis of their optical and thermal properties. When exposed to UV light, the photoactive polymer films can develop a deep blue color (566 nm in the absorption spectra). Finally, the study also assesses their capacity for photodynamic antimicrobial action in organic film. Notably, the photoactive P(MAn-alt-2MB)-PS significantly enhances the photodynamic antimicrobial activity of the photosensitizer Ru(bpy) against two bacterial strains of Staphylococcus aureus, reducing the minimum inhibitory concentration (MIC) from 2 µg/mL to 0.5 µg/mL. Therefore, 4 times less photosensitizer is required when mixed with the photoactive polymer to inhibit the growth of antibiotic-sensitive and -resistant bacteria. Full article

Microencapsulated phase-change materials (MPCMs) with excellent thermal properties for low-temperature cold storage were developed in this study. Using 1-decanol as the core and methyl methacrylate as the shell precursor, the effects of emulsifier type and ultrasonic emulsification conditions were investigated. Styrene-maleic anhydride copolymer served effectively as a protective colloid emulsifier, producing MPCMs with high enthalpy and a well-defined, uniform microstructure. Under optimal conditions of 5 wt% emulsifier content relative to the oil phase, an ultrasonic power of 375 W, and an emulsification time of 12 min, the MPCMs exhibited a phase-change enthalpy of 126.7 kJ/kg. To further improve the thermal properties, a binary eutectic mixture was prepared by combining 1-decanol and 1-tetradecane at an optimal molar ratio (51.1:48.9). This binary-core MPCM showed a higher storage enthalpy (144.3 kJ/kg), with an increase of 13.9% compared to the single-core material (1-decanol). It also exhibited improved microstructural uniformity due to the stabilizing role of 1-tetradecane. These optimized MPCMs demonstrate phase-transition temperatures particularly suitable for low-temperature thermal storage, providing a practical and innovative technical solution for cold-chain logistics and vaccine refrigeration applications. Full article

Synthetic plastic impacts the environment due to its slow degradation and the generation of microplastics, driving the development of bioplastics. This study evaluated the use of bagasse fiber combined with corn and potato starch to improve the physical and mechanical properties of bioplastics. Five bioplastic mixtures (Am1 to Am5) were prepared with corn starch, glycerin, acetic acid, maleic anhydride, and agave bagasse. Am1 was prepared without bagasse, and the others were prepared with different amounts of bagasse (0, 10, 30, 50, and 70 g). Bioplastics made from potato starch (Ap1 to Ap5) were also produced under the same conditions and were assessed using the thermogravimetric (TGA) and scanning electron microscopy (SEM) tests. Analysis of variance showed significant differences (p < 0.001) in the moisture, Young’s modulus, and stress of the bioplastics. The corn-based bioplastics exhibited lower moisture values (7.26% and 5.51%) compared to the potato-based ones (9.68% to 8.89%). Young’s modulus and stress increased in the corn-based (Am5 = 4.59 MPa) and potato-based (Ap5 = 3.53 MPa) bioplastics with higher amounts of bagasse. Furthermore, TGA and SEM revealed the surface morphology and the effects of processing, and based on their results, it was found that agave bagasse improved the mechanical and thermal properties of bioplastics, especially corn-based ones, suggesting its potential as a material with a lower environmental impact. Full article

Poly (styrene-maleic anhydride) copolymers, due to their unique structure, are extensively functionalized and modified for preparing heat stabilizers, compatibilizers, and other functional additives. Using 4-methylpent-1-ene-2,4-diyl diphenyl (α-MSD) as a chain transfer agent, a series of molecular-weight-controlled maleic anhydride-derived styrene copolymers, poly(N-p-fluorophenylmaleimide-alt-styrene) (PFS) and poly(N-p-carboxylphenylmaleimide-alt-styrene) (PCS), were synthesized via free radical copolymerization. The molecular weights of PFS and PCS were adjusted to explore their impact on the properties of PFS/PA6 and PCS/PA6 blends. Gel permeation chromatography (GPC) analysis confirmed that α-MSD effectively regulated the molecular weights of PFS and PCS. PFS and PCS with lower molecular weights exhibited significantly reduced viscosity, with minimal impact on their thermal and mechanical properties. Full article

The reuse of recycled carbon fibers (rCF) is a response to growing environmental concerns associated with the composites industry. Recycling and reusing carbon fibers represents a more sustainable alternative by reducing waste at the end of the life cycle of composite materials and decreasing dependency on virgin raw materials. This study investigates the influence of process parameters on two different non-woven mats made by carding rCF and blending with thermoplastic filaments: Carbiso TM-PA6/60 and TM-MAPP/60. Two processing methods were examined—one-shot process (M1) and lamination (M2)—to fabricate multilayer coupons. The results indicate that the two-layer panels produced using M2 exhibited a lower porosity (9.9% for PA6/60 and 4.1 for MAPP/60) and superior mechanical performance. However, the differences in performance between the two methods diminished as the number of layers increased. Concerning matrix–fiber compatibility, MAPP/60 showed the best results due to the fiber’s roughness, matrix particles on the fibers, and the incorporation of maleic anhydride in polypropylene (PP), significantly enhancing adhesion. Full article