Polymer Components Research Articles

Advancements in Dental Bioreactor Design: A Comprehensive Approach for Application in Dentistry.

The protocol introduces a novel multi-chamber bioreactor tailored for ex-vivo cell culture in dentistry research, emulating the 3D dental environment to propel research in dental applications. Constructed primarily from a polymeric material with a sophisticated 3D design, the bioreactor securely holds teeth structures within sealed chambers, enabling controlled perfusion of culture medium crucial for cell growth through a singular entry and exit point. An integrated electronic system manages flow and pressure, ensuring precise control over environmental conditions. This technology facilitates cell cultivation under conditions closely resembling natural tooth microenvironments, offering opportunities for varied studies from understanding cellular behavior in dental contexts to targeted therapy development. The bioreactor's amalgamation of polymeric components, 3D design, and electronic controls enhances adaptability and accuracy, rendering it a valuable asset in dental research. The report comprehensively delineates the bioreactor's design, operations, and potential applications, showcasing its significant contributions to dental research and regenerative medicine. By amalgamating advanced technologies, this bioreactor emerges as a pivotal tool for investigating cellular processes within dental structures, paving the way for scientific exploration and therapeutic advancements.

Renewable Fuels and Chemical Recycling of Plastics via Hydrothermal Liquefaction.

ConspectusHydrothermal liquefaction (HTL) converts a wide range of biomass feedstocks into a renewable bio-oil via reactions in hot, compressed water. Other products that form partition into the gas, aqueous, or solid phases. The reactions taking place during HTL include hydrolysis, decarboxylation, condensations, additions, deamination, and dehydration. Bio-oil production from HTL has been demonstrated for many renewable materials including microalgae, macroalgae, sludge from water treatment, food waste, agricultural residues, bacteria, yeast, and a wide variety of lignocellulosic materials. HTL of whole biomass is an energy densification process as it generally recovers about 70-80% of chemical energy in an oil product that is just 20-50 wt % of the mass of the original feedstock. The oil is typically rich in oxygen (10 -20 wt %) and also in nitrogen (about 5 wt %), if the biomass contains protein. The oil also contains metals such as iron. Therefore, an upgrading and/or refining process would be required to convert the crude bio-oil to a finished fuel. Each biochemical component in biomass (e.g., polysaccharides, protein, lipids, lignin) contributes different proportions of its initial mass to biocrude. Lipids provide the highest biocrude yields whereas polysaccharides and lignin provide the lowest. Kinetics models have been developed that incorporate different reactivities for the different biochemical components. These models, which are effective in correlating and predicting the yields of biocrude and other product fractions from HTL, can be used in technoeconomic analysis and life-cycle assessments to advance commercial adoption of the technology.HTL is also effective in producing an oil product from decomposition of many different plastics. Thus, it can be used for chemical recycling or valorization of post-consumer waste plastics. Polyolefins and polycarbonates can give oil yields exceeding 90 wt %. Polyethylene terephthalate (PET) gives very low oil yields. The major product from PET hydrolysis, terephthalic acid, is a solid at room temperature and not soluble in the organic solvents typically used to recover oil.Hydrothermal decomposition of isolated biochemical components of biomass and individual synthetic polymers provides insights into the governing chemical reaction pathways. Results from such experiments also enable development of component additivity models that can predict oil yields and other outcomes from HTL of biomass, plastics, and their mixtures.Research needs in this field include more detailed, molecular-level kinetics models, experimental work on HTL and hydrolysis of the many synthetic plastics that have not yet been adequately explored, and experiments and modeling for mixtures of different plastics and mixtures of plastics with biomass.

Damage evaluation in plain-woven CFRP plate with circular hole under cyclic tensile loading using electrical impedance tomography

Understanding and predicting damage progression within thin plain-woven carbon fiber-reinforced polymer (CFRP) components is an essential issue for scheduling maintenance intervals and structural inspections and typically requires extensive test series. However, uncertainties always remain and result in conservative design and unnecessary downtimes due to the repeated inspections of a healthy structure. Structural health monitoring (SHM) can be used to reduce these uncertainties, as it allows one to evaluate the condition of a mechanical structure during operation. Numerous SHM methods have been developed, which achieve different levels of damage identification but are often investigated at small coupons with nonrealistic structural damages and loading conditions on both structure and sensor. The present research investigates electrical impedance tomography (EIT) featuring an elastoresistive thin-film sensor to evaluate damage that propagates from a circular hole in a large plate under cyclic tensile–tensile multiblock loading. Applied fatigue loads were increased multiple times up to a total number of two million cycles. During the loading, damage initiated at the hole and continuously propagated into the plate. Repeated EIT evaluations of the applied sensor and validating evaluations by means of digital image correlation clearly revealed the robustness of the hardware and the potential of the SHM method for damage evaluation of plain-woven CFRP components.

Molecular models of PM6 for non-fullerene acceptor organic solar cells: How DAD and ADA structures impact charge separation and charge recombination.

The quadrupole moment of a non-fullerene acceptor (NFA) generated by the constituent electron donor (D) and acceptor (A) units is a significant factor that affects the charge separation (CS) and charge recombination (CR) processes in organic photovoltaics (OPVs). However, its impact on p-type polymer domains remains unclear. In this study, we synthesized p-type molecules, namely acceptor-donor-acceptor (ADA) and donor-acceptor-donor (DAD), which are components of the benchmark PM6 polymer (D: benzodithiophene and A: dioxobenzodithiophene). Planar heterojunction films, a model of bulk heterojunction, were prepared using ADA, DAD, and PM6 as the bottom p-type layers and Y6 NFA as the top n-type layer. Flash-photolysis time-resolved microwave conductivity, femtosecond transient absorption spectroscopy, and quantum mechanical calculations were employed to probe the charge carrier dynamics. Our findings reveal that while the subtle difference in quadrupole moment and energy gradient of the p-type materials has a minimal influence on CS, the molecular type (ADA or DAD) significantly affects the bulk CR. This study expands the understanding of how the p-type component and its conformation at the p/n interface impact the CS and CR in OPVs, highlighting the critical role of molecular donors in optimizing device performance.

Design and validation of fixation points of polymeric components for the automotive industry

ABSTRACT The incorporation of polymeric materials in car structure components plays a key role in the automotive sector, enabling the production of more efficient and ecological vehicles. Among the many options to fix these components, there are clips and snap-fits, which not only facilitate assembly and disassembly, but also contribute to reduce the total mass of the car. This work aims to design and validate these fixation points of polymeric components using the Design Science Research (DSR) methodology. The work resulted from the need for a more rigorous control involving some internal standardized fixation points, namely interior trim parts. Experimental tests were carried out according to the specifications of the automotive brand, including the strength of the fixation points, to enable incorporation as standard components. Using the Finite Element Method (FEM), static simulations were performed in the Abaqus® software, where the conditions of the physical tests were replicated to correlate both tests and validate the numerical approach. Improvement of the fixation points was next undertaken, by making changes in the areas that were identified as critical. The improved fixation points were able to meet the specifications of the company and were proposed as new geometry for standard interior trim parts.

Influence of halloysite nanotubes on processing, structural and thermal properties of poly(vinyl chloride)/high-density polyethylene composites with wood flour

ABSTRACT The aim of this work was to investigate the effect of halloysite nanotubes (HNT) on the processing, structural and thermal properties of poly(vinyl chloride) (PVC), high-density polyethylene (HDPE), and PVC–HDPE composites with various proportions of both polymer components containing 30 wt% wood flour (WF) and 5 wt% halloysite processed in the Brabender measuring mixer. The HNT content in the composites leads to a slight increase in the maximum torque and a reduction in the gelation time for PVC and PVC–HDPE matrix composites with the 90:10 component ratio. In addition, microscopic images of these materials showed a homogeneous distribution of HNT in the polymer matrix. The addition of mineral filler to the matrix, regardless of the polymer type, resulted in a slight increase in the torque values at the kneading endpoint. The PVC–HDPE–wood flour composites are characterized by higher thermal stability at processing temperature when HNT is loaded. The introduction of 5 wt% HNT into the PVC–HDPE 90:10 30 wt% WF blend resulted in an increase of the 2% weight loss temperature by 16°C. The simultaneous use of wood flour and halloysite as fillers for PVC–HDPE blends could be an eco-efficient solution for the new composite material sector.

The influence of external and internal factors on ensuring adhesive interaction of a polymeric sealant with a substrate surface (a review)

This paper analyzes literature data on the influence of various factors affecting the strength and durability of adhesive bonds, as well as presents a characterization of the methods described in the literature for conducting relevant studies. It is shown that one of the main characteristics of adhesive joints is the interaction at the interface between the substrate and the adhesive. The adhesive capability of a sealant largely depends on the structure of the polymer component, as well as the presence of components in the sealant that enhance this property. The structure and condition of the substrate surface significantly affect the nature of the interaction between the adhesive and the substrate. Various methods are used to determine the strength of the adhesive bond, differing in the type of applied loads and the nature of the surface fracture. An important indicator is the determination of the wetting angle of the substrate by the sealant, which characterizes the surface energy. The durability of adhesive bonds is significantly influenced by environmental factors as well as operational conditions. Moisture, atmospheric oxygen, ultraviolet radiation, and microorganisms have a particularly strong effect on the properties of polymeric sealants.

Repurposing trityl-substituted triphenylamine-based polyimides for gas separation membranes by blending with a fluorinated polyimide

In the attempt to develop gas separation membranes by reusing polymers with no film-forming ability but with great potential for this purpose, blending has been approached as a simple, time- and cost-effective strategy. Herein, blends of trityl-substituted triphenylamine (TTA)-based polyimides and a fluorinated polyimide (6F-PI) were involved to prepare dense membranes by drop-casting technique. The two blend components involved in variable amounts led to different film morphologies with a strong impact on most blends' properties and gas separation performance. According to optical microscopy, SEM, AFM, and FTIR investigations, the blend series containing hexafluoroisopropylidene (6F) groups in both polyimide components proved to be fully miscible at the molecular levels. When a single 6F-based component was integrated into the blend, the polymers proved to be compatible, but only partially miscible, with a two-phase structure, in which 6F-PI wrapped around the TTA-PI growth fibrillar domains. However, all blends displayed a single glass transition and FTIR bands which do not sum the ones of the polymer components, as well as a high thermal stability, close to that of 6F-PI. Regardless of their miscibility level, all blends behaved as classical polyimide films, with good mechanical properties and chemical resistance to corrosive media like acid vapors or basic solutions. The blend composition and diimide structure of TTA-PI little affected the dielectric behavior, unlike the gas separation performance that strongly depended on these characteristics. The higher amount of 6F groups in the miscible blends endowed the membranes with superior permeability and selectivity, allowing in some cases to surpass the trade-off rule. Generally, the gas permeability decreased with the increase of TTA-PI content, with some exceptions. The low intermolecular interfacial interactions promoted by TTA-PI were found to be beneficial in preserving a good selectivity of gas molecules with a small kinetic diameter (He, CO2) though their permeability is lost. The gas permeability changes as a function of the blend composition and structure were mostly due to changes in the solubility coefficient and less from gas diffusion capability, at least for CO2 and N2.

Mechanical Strength of Additive Manufactured and Standard Polymeric Components Joined Through Structural Adhesives.

The main aim of this work is to evaluate the mechanical properties of additive manufactured polymeric parts joined with standard plastic parts through structural adhesives. The primary advantage of this technique is its ability to significantly increase the size of the final assembly by using additive manufacturing (AM) for complex joints and inexpensive, reliable extruded plastic parts for load-bearing components. This hybrid assembly combines the flexibility and shape adaptability of AM with the structural strength and cost-effectiveness of extruded polymer parts, resulting in a final design that performs comparably to the base material. The materials used in the paper are rigid acrylic adhesive and toughened acrylic, both applicable with almost no surface preparation and fast curing. The 3D-printed parts are produced in ABS, while the standard parts are in PVC. First, the work is devoted to estimating the performance of the adhesives using pin-collar joints and a combined numerical and experimental methodology. The second section presents and discusses the results of two more realistic applications of adhesive bonding to hybrid complex joints. For the pin-collar joints, the results show failure mostly in the adhesive, with an average shear stress of 11.5 MPa and 5.22 MPa and a stiffness of 4449 N/mm and 3649 N/mm for the rigid and toughened adhesives, respectively. The results of the adhesive bonding of structural joints show that the adhesive is always capable of providing the load-carrying capacity required to achieve the strength of traditionally manufactured polymeric parts. The paper shows that adhesives are a feasible way to expand the potential of 3D-printed equipment to obtain larger hybrid parts partially realized with traditional technology, especially with inexpensive off-the-shelf bars and sections.

A Flexible Organomagnetic Single-Layer Composite Film with Built-In Multistimuli Responsivity.

Materials possessing multiple properties and functionalities, that can be controlled or modulated by external stimuli, are a central focus of current research in materials sciences due to their potential to significantly enhance various future technological applications. Herein, we report a significant advancement in this field through the development of a smart, multifunctional organomagnetic composite material. By utilizing a thin layer of polydimethylsiloxane (PDMS) and polypyrrole (PPy) precursors, doped with nickel nanoparticles (NiNPs), we have created an innovative organomagnetic, PDMS/PPy/NiNPs (PPN), single-layer composite film that displays multistimuli responsivity. The study presents the first demonstration of a multifunctional flexible, three-component film structure integrating the structural and flexible PDMS component, together with a conductive polymer component and metal-based nanoparticles into a single-layer design, which displays enhanced and unprecedented responsivity properties against multiple different stimuli. Unlike typical stacked multilayered structures, that exhibit one or two functionalities at most, this novel configuration exhibits multiple functionalities, including magnetoresistance, mechanical stress response, piezoresistivity, and temperature change sensitivity. The as-prepared film demonstrates notable magnetoresistance responsivity, with a relative electrical resistance, ΔR/R0, changing under a weak magnetic field and under ambient conditions. The significance of our study lies in the film's versatility, stability, and sensitivity, especially within the physiological temperature range, making it highly relevant for future biomedical applications. Furthemore, the film's sensitivity to mechanical deformation reveals an impressive piezoresistance behavior. Unlike existing multilayer architectures of higher complexity, our single-layer thin film offers a simpler, more flexible, and reliable solution with a broad range of stimuli-sensing capabilities. The significance of this novel multiresponsive composite material is underscored by the growing demand for advanced materials in biomedical devices, magnetic switches, sensors, electronic skin, transistors, and organic spintronic devices. These promising organomagnetic self-standing layers provide a robust platform for future technological innovations.

Development of chitosan-acrylic acid based hydrogels with incorporated polyaniline and plasma treatment

Hybrid hydrogels are materials that incorporate features from multicomponent systems of polymers, significantly improving their functionality and making them ideal for biomedical applications. Both natural and synthetic polymers are utilized, further enhancing their functionality. The combination of polyaniline (PANI), chitosan (CS), and acrylic acid (AA) can result in a multifunctional hybrid hydrogel that is antibacterial, hydrophilic, and salt-sensitive. A multifunctional PANI-CS-AA with varying PANI weight ratio was synthesized in this study. In addition, improving the surface of the multifunctional hydrogels by atmospheric pressure plasma (APP) treatment was also investigated. During APP treatment, the production of reactive species (e.g., OH and N2 radicals) responsible for the functionalization of the hydrogel surface was confirmed through optical emission spectroscopy. The integration of three polymer components in the synthesized hydrogels was confirmed through the presence of their mid-FTIR spectral characteristics, particularly in the AA and CS C=O, PANI quinonoid and benzenoid units, AA COO−, and the PANI aromatic and C—H vibration regions. Moreover, the hybrid hydrogels with incorporated PANI and APP treatment improved their wettability and surface free energy (SFE) characteristics. The hybrid hydrogels with 0.25 wt. % PANI and exposed to 2 min air plasma yielded the highest hydrophilicity and total SFE with values 41.27° ± 2.15° and 135.68 ± 4.72 mJ/m2, respectively. The plasma-treated 0.25PANI-2.5CS-4AA samples exhibit improved swelling response in water (Smax = 1310 ± 100; ks = 0.005) and saline media (Smax = 1280 ± 80; ks = 0.001) due to enhanced polymeric chains and affinity toward polar liquids. Synthesized hydrogels exhibited antibacterial activity, as evidenced by the zone of inhibition test. Clearing zones measured were in the range of 16–27 mm. The study developed an APP-treated tricomponent hydrogel consisting of PANI, CS, and AA that has improved hydrophilicity, salt sensitivity, and antibacterial features.

Polymer-Interface-Tissue Model to Estimate Leachable Release from Medical Devices.

The ability to predict clinically relevant exposure to potentially hazardous compounds that can leach from polymeric components can help reduce testing needed to evaluate the biocompatibility of medical devices. In this manuscript, we compare two physics-based exposure models: 1) a simple, one-component model that assumes the only barrier to leaching is the migration of the compound through the polymer matrix and 2) a more clinically relevant, two-component model that also considers partitioning across the polymer-tissue interface and migration in the tissue away from the interface. Using data from the literature, the variation of the model parameters with key material properties were established, enabling the models to be applied to a wide range of combinations of leachable compound, polymer matrix and tissue type. Exposure predictions based on the models suggest that the models are indistinguishable over much of the range of clinically relevant scenarios. However, for systems with low partitioning and/or slow tissue diffusion, the two-component model predicted up to three orders of magnitude less mass release over the same time period. Thus, despite the added complexity, in some scenarios it can be beneficial to use the two-component model to provide more clinically relevant estimates of exposure to leachable substances from implanted devices.

Fully Atom-Efficient Solvent-Mediated Biopolymer Manufacturing: A Base Case Illustrated with Macromolecular Surfactants Tailored to Stable Polymer-Water Interfaces.

This work introduces a novel 1-pot, 0-waste, 0-VOC methodology for synthesizing polymeric surfactants using acrylated epoxidized soybean oil and acrylated glycerol as primary monomers. These macromolecular surfactants are synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization, allowing for tunable hydrophilic-lipophilic balance (HLB) and ionic properties. We characterize the copolymers' chemical composition and surface-active properties, and evaluate their effectiveness in forming and stabilizing emulsions of semiepoxidized soybean oil and poly(acrylated epoxidized high oleic soybean oil). Comprehensive analyses, including gel permeation chromatography, nuclear magnetic resonance spectroscopy, dynamic light scattering, particle size distribution, zeta potential, and critical micelle concentration, provide detailed insights into the copolymers and the emulsions they form. The results demonstrate that the RAFT-polymerized surfactants offer long-lasting stability and effectively disperse both common oil-in-water emulsions and highly viscous and hydrophobic polymer latexes. These surfactants outperform traditional small molecule surfactants by reducing particle size and preventing phase separation, even over extended storage periods. Stable polymer-water interfaces are achieved through HLB control, tailored by monomer composition, and the final product requires no additional purification since polymerization occurs in liquid surfactants. While small molecules contribute to rapid micelle formation, the polymeric components enhance long-term stability through steric repulsion and slower dynamics. This method enables even the emulsification of polymers with submicron particle size, which ordinarily requires emulsion polymerization. Integrating biobased polymeric surfactants with advanced polymer processing techniques opens new possibilities for transforming highly hydrophobic polymers into latexes, facilitating downstream applications. This innovation enhances the environmental sustainability of surfactant production and broadens the potential for polymer emulsification technologies. Additionally, the integrated solution-processing approach demonstrated here can be applied to other emerging polymers, where judiciously selected nonvolatile solvents facilitate the polymerization and play a role in the final application.

Simultaneous strengthening and toughening of PLA with full recyclability enabled by resin-microsphere-modified L-lactide oligomers

Various strategies have been developed to improve the brittleness of poly (lactic acid) (PLA), most of which still suffer from the toughness-strength trade-off dilemma. Herein, we prepared phenol–formaldehyde-resin microspheres (PFM) with aliphatic hydroxyl groups to initiate L-lactide polymerization and synthesized a series of PFM-modified L-lactide oligomers (PFM-OLLA) bearing different arm lengths. PFM-OLLA were then physically blended with commercial PLA in different weight ratios to prepare synchronously strengthened and toughened PFM-OLLA/PLA composites. After blending with 4 % PFM2.5-OLLA (PFM content: 2.5 %), the mechanical properties of the PFM2.5-OLLA/PLA composites were best. PFM2.5-OLLA efficiently improved the crystallization behaviors of the PFM2.5-OLLA/PLA composites, thereby significantly enhancing their strength and toughness. The maximum tensile yield strength (40.2 MPa), elongation at break (85.7 %), and impact strength (20.8 kJ/m2) of PFM2.5-OLLA/PLA composites could respectively increase by 44.2 %, 465.7 %, and 100 %, compared to the values of neat PLA. The microscopic strengthening and toughening mechanisms were attributed to the rigidity of PFM, and the heterogeneous nucleating ability as well as larger free volume of PFM2.5-OLLA, whereas the visual toughening effects were attributed to multiple crazing and shear yielding phenomena. After simple alcoholysis and filtration, the polymer components were completely converted into methyl lactate. The recycled PFM, exhibiting excellent chemical stability, were reused to synthesize a new PFM-OLLA for strengthening and toughening PLA. This study provides a sustainable strategy for the development of high-performance PLA engineering materials showing great application potentials in the automotive, electronics and housing fields.

State-of-the-art Review of Springback Behavior of Polymers

The spring-in and spring-back behavior of polymers is intricate and influenced by various process parameters and mechanisms, including interply slip, anisotropic thermal expansion, and crystallization, all of which can lead to residual stresses. Composite materials made of metal and polymer are being investigated by researchers as a promising alternative to monometallic materials due to their superior properties. However, the number of studies related to metal/polymer/metal laminates on the same topics is relatively limited. A comprehensive review study was carried out with a focus on research works that were conducted with the consideration of different process parameters, such as radius of die and punch, friction, and force applied by blank holder, in order to observe their impact on the springback behavior of polymers. Springback on polymer components depends on the accuracy of appropriate materials and the consideration of appropriate experimental strategies. However, due to their viscoelastic properties, polymers demonstrate distinctive springback behavior. Furthermore, when subjected to deformation, polymers experience a combination of elastic and viscous responses, resulting in immediate elastic recovery and time-dependent viscoelastic relaxation. This intricate behavior presents difficulties in precisely forecasting and managing springback. To enhance the control and optimization of springback in polymer-based manufacturing processes, it is essential to improve the understanding of polymer behavior under diverse loading conditions and to refine simulation techniques accordingly. This review focuses on springback prediction models specific to polymers.

The Transformative Role of Nano-SiO2 in Polymer Electrolytes for Enhanced Energy Storage Solutions

In lithium–polymer batteries, the electrolyte is an essential component that plays a crucial role in ion transport and has a substantial impact on the battery’s overall performance, stability, and efficiency. This article presents a detailed study on developing nanostructured composite polymer electrolytes (NCPEs), prepared using the solvent casting technique. The materials selected for this investigation include poly(vinyl chloride) (PVC) as the host polymer, lithium bromide (LiBr) as the salt, and silica (SiO2) as the nanofiller. The addition of nano-SiO2 dramatically enhanced the ionic conductivity of the electrolytes, with the highest value of 6.2 × 10−5 Scm−1 observed for the sample containing 7.5 wt% nano-SiO2. This improvement is attributed to an increased amorphicity resulting from the interactions between the polymer, salt, and filler components. A structural analysis of the prepared NCPEs using X-ray diffraction revealed the presence of both crystalline and amorphous phases, further validating the enhanced ionic transport. Additionally, the thermal stability of the NCPEs was found to be excellent, withstanding temperatures up to 334 °C, thereby reinforcing their potential application in lithium–polymer batteries. This work explores the electrochemical performance of a fabricated lithium-ion-conducting primary electrochemical cell (Zn + ZnSO4·7H2O|PVC: LiBr: SiO2|PbO2 + V2O5), which demonstrated an open circuit voltage of 2.15 V. The discharge characteristics of the fabricated cell were thoroughly studied, showcasing the promising potential of these NCPEs. With the support of superior morphological and electrical properties, as-prepared electrolytes offer an effective pathway for future advancements in lithium–polymer battery technology, making them a highly viable candidate for enhanced energy storage solutions.

Closed-loop recyclable wood-plastic composite as a sustainable alternative to wood: A solution for utilizing wood waste and promoting carbon sequestration

Utilizing wood waste to construct high-performance materials and partially replace natural wood applications is a feasible solution to address the overconsumption of forest resources and enhance carbon sequestration. A closed-loop recyclable wood-plastic composite (WPC) with high wood waste flour (WF) content (70 wt%) was developed using poly(p-dioxanone) (PPDO) as the polymer component. The two components in WF/PPDO WPC form an interesting symbiotic relationship owing to their strong interactions. PPDO serves as “binder” for WF and integrates them as a whole, whilst WF protects PPDO from hydrolysis, therefore substantially prolonging service life. The comprehensive performance of the WF/PPDO WPC (such as WF content, mechanical properties, hardness, and water absorption) is comparable or better than natural wood or commercial WPC. Moreover, WF/PPDO can be closed-loop recycled almost 100 % to its initial raw materials. The relatively low carbon footprint of WF/PPDO (1.06 kg CO2e/kg of materials) was confirmed by life-cycle assessment (LCA). In addition, the facile preparation of WF/PPDO is scalable and widely applicable to other cellulose-containing waste.

Fluorimetric Detection of Vapor Pollutants with Diketopyrrolopyrrole Polymer Microcavities.

The increasing prevalence and detrimental effects of volatile organic compounds are driving the need for selective on-site sensors that do not require complex sampling or instrumentation. Broadband selective sensors exhibiting selectivity based on their distinct response mechanism is becoming of increasing technological relevance in both industrial and urban settings. In this context, we propose a label-free sensor based on a polymeric planar microcavity embedded with a fluorescent organic dye, designed to detect various pollutants in the vapor phase. The sensor consists of alternating layers of cellulose acetate and poly(N-vinylcarbazole) and contains a polystyrene defect layer doped with a quadrupolar diketopyrrolopyrrole. Both the structural properties of the polymer microcavity and the dye in the defect layer contribute to the sensor's response to analytes, creating a dual-probe system where a single photonic element translates chemical signals into optical signals, namely, transmission and fluorescence spectral variations. The discrimination capability of the photonic structure arises from the physicochemical interactions between the analytes and the polymer components. To validate our approach, we evaluate the sensor's response to four distinct volatile molecules and investigate the mechanisms influencing the optical response.

Occurrence and spatial distribution of microplastics in water and sediments of Hatiya Island, Bangladesh and their risk assessment

This research has evaluated the MPs distribution, characteristics, and potential threats of MPs in surface water and sediments from Hatiya Island. The results showed that the abundance of MPs was 139 ± 44 items/m3 in surface water and 493 ± 80 items/kg dw in sediments, indicating higher levels of MPs contamination in sediment samples. Fibers were the predominant kind of microplastics, and microscopic sizes (0.3–1.5 mm) MPs were generally more frequent and largely present in both the surface water and sediments. Fourier-transform infrared spectroscopy (FTIR) confirmed that polyethylene terephthalate was the major polymer component of microplastics in surface water, whereas polyethylene was the most abundant polymer in sediments. MPs contamination risk was examined based on multiple risk assessment models. Nemerow pollution index (NPI) and pollutant load index (PLI) show minimal pollution levels of MPs. But potential hazard index (PHI), potential ecological risk factor (Er), and potential ecological risk index (RI), indicate severe MPs contamination due to the presence of polyurethane, polycarbonate, polyvinyl chloride, epoxy that were hazardous MPs and exhibited a critical concern for MPs risk. These statistics will help to understand the environmental difficulties generated by MPs and which hazard is waiting for mankind in the future.

A comprehensive risk assessment of microplastics in soil, water, and atmosphere: Implications for human health and environmental safety

Microplastics (MPs) are pervasive across ecosystems, likely posing significant environmental and health risks based on more and more evidence. In this study, we searched through the Web of Science Core Collection and obtained 1039 papers for visualization and analysis. In order to discuss the chemical composition, migration, transformation and potential risk of MPs, 135 sets of relevant data in soil, water, and atmosphere were collected in China as a typical region, which is a hotspot region for investigation of MPs. The results showed that the primary polymer categories of MPs in the environment to be polypropylene, polyethylene, and polystyrene. The soil contains a significant quantity of MPs, averaging at 12,107.42 items·kgdw−1, while water contains averaging at 97,271.18 items m−3. The total pollution load indexes for all three environments are at risk level I. Based on current risk assessment methods, the potential ecological risk of MPs is low. However, based on the polymer components, migration and transformation patterns, and especially the complexes with other pollutants, it indicates an increasing indirect risk. Interactions with some other pollutants are likely amplify the ecological and health risks associated with MPs. Aggregative results showed that the present risk assessment models could not assess the risks of MPs well. Thus, we suggested develop a risk assessment methodology for MPs based on relevant research progress. Some factors such as the size and form of MPs, sources and distribution, bioaccumulation, social acceptance and economic costs could be considered adding in the present risk assessment models. Finally, promotion of development and application of green chemically synthesized bioplastics such as using synthetic biology to help degrade plastics would be an alternative and sustainable option to relieve the adverse environmental and health concerns of MPs.