Search Results (186)

This paper focuses on developing reinforced self-healing supramolecular resins that meet both functional and structural needs for industrial use. The formulated advanced nanocomposites are made from compounds that allow for reversible self-healing interactions. The self-healing molecules bond with the toughened epoxy matrix using hydrogen bonding. To enhance the epoxy’s typical insulating properties, electrically conductive carbon nanotubes (CNTs) were added to achieve an electrical percolation threshold (EPT) with a low amount of nanofiller. This study found that self-healing efficiency can reach nearly 99%. The addition of healing compounds significantly raises the glass transition temperature to over 200 °C. Tunneling Atomic Force Microscopy (TUNA), which is an innovative tool for correlating local topography with electrical properties, reveals the structural properties and compatibility of these materials, mapping conductive pathways at the micro- and nanoscale. Full article

The present research article deals with the thermal degradation study of epoxy resins filled with hybrid nanostructured forms of carbon under oxidative conditions. In particular, the formulated polymer composites (denoted as HYB_0.1%_CNTs:GNs and HYB_0.5%_CNTs:GNs, respectively) consist of two kinds of fillers, namely multi-walled carbon nanotubes (CNTs) and graphene nanosheets (GNs), mixed together with two different total mass amounts: 0.1 and 0.5%. In both kinds of nanocomposites, three different CNT:GN mixing ratios were considered (5:1, 1:1, and 1:5, respectively), thus providing a total of six hybrid samples. The thermal behavior of these samples was studied by simultaneous thermogravimetry and differential thermal analysis (TG/DTA) under flowing air, and two processes took place in distinct temperature ranges. In each step, about 50% of mass loss is detected with an exothermic effect in the corresponding DTA curve, with the second one accompanied by an intense heat release. The kinetic analysis of the two-stage oxidative thermal degradation was investigated using a model-free isoconversional approach. A non-Arrhenian behavior of the temperature function k(T) was assumed, and lifetime prediction was estimated at temperatures close to those of the possible applications. Isoconversional analysis shows nearly constant activation energies for all composites except HYB_0.1%_5:1 (from 142 to 96 kJ·mol⁻¹), while lifetime predictions indicate that thermal stability increases with graphene content at 0.1% loading (HYB_0.1%_1:5) and with CNT content at 0.5% loading (HYB_0.5%_5:1), with uncertainties below 7%. Finally, because of the π–π bond interactions between the CNTs and the GNs dispersed in the epoxy resin matrix, an effective and remarkable electrical performance was found and a correlation with both electrical and morphological properties was established. In this regard, Tunneling Atomic Force Microscopy (TUNA) proved to be particularly powerful in allowing the simultaneous mapping of topography and localized conductive networks with exceptional sensitivity to nanofiller dispersion, such as CNTs and GNs. DC conductivity increased by up to nine orders of magnitude at 0.1 wt% hybrid loading (up to 3.73 × 10⁻⁴ S/m vs. 1.06 × 10⁻¹³ S/m for CNT-only), with nanoscale TUNA currents (−1.9 to 4.5 pA) mirroring macroscopic trends, while at 0.5 wt% all hybrids reached 10⁻² S/m, indicating reduced synergy once a fully developed conductive network is established. Full article

This study successfully developed an efficient one-dimensional confinement strategy to encapsulate polyoxometalate NiMo₆ clusters densely and uniformly within the cavities of a single-walled carbon nanotube (SWCNT), constructing a unique core–shell NiMo₆@SWCNT composite electrocatalyst. Comprehensive characterization including high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), and ultraviolet-visible absorption spectroscopy (UV-Vis) systematically confirmed the uniform dispersion and structural integrity of NiMo₆ within the SWCNT channels. Key evidence encompasses: (1) EDS elemental mapping revealing high co-localization of Ni/Mo signals inside the lumens; (2) transmission electron microscopy (TEM) images confirming the effectiveness of the filling process. The composite achieved an exceptionally low overpotential of 308 mV to drive a current density of 10 mA cm⁻² (significantly outperforming pure NiMo₆ at 365 mV and pristine SWCNT at 519 mV), exhibited a remarkably low Tafel slope of 96.64 mV dec⁻¹, possessed a high electrochemical active surface area (10.75 mF cm⁻²), and very low charge transfer resistance. Critically, it showed negligible current density decay during prolonged chronoamperometric operation over 35,000 s (>9.7 h). This work not only validates the confined encapsulation as a viable strategy for fabricating highly active polyoxometalate/carbon composites, but also elucidates that the performance enhancement stems from a “triple synergy”: the intrinsic catalytic activity of NiMo₆, the highly conductive/mass-transport network provided by SWCNT, and the synergistic effects arising from the confined interface—namely stress regulation and electronic coupling. This insight provides a novel perspective for designing high-performance non-precious metal electrocatalysts. Full article

Silica aerogels are ideal candidates for gas adsorption due to their exceptional porosity and high specific surface area; however, the inherent mechanical fragility of their skeletal framework significantly compromises their operational stability in engineering applications. While the incorporation of carbon nanomaterials effectively enhances the mechanical robustness of aerogels, the specific microscopic mechanisms by which filler microstructure and surface chemistry dictate gas adsorption behavior remain insufficiently understood. In this study, we employed all-atom molecular dynamics (MD) simulations to develop a model of silicon-based porous composites synergistically doped with carbon nanotubes (CNTs) and graphene. The adsorption and diffusion characteristics of nitrogen (N₂) were systematically investigated across a CNT doping concentration range of 5% to 20%, and the influence of surface hydrophilicity/hydrophobicity on adsorption performance was quantitatively analyzed by modulating potential energy parameters. Our results demonstrate that the introduction of CNTs reconfigures the porous architecture, leading to an approximately 18.25% increase in the normalized specific surface area, which subsequently drives a 15% enhancement in the overall adsorption capacity of the composite. Nevertheless, analysis reveals that the weight-specific adsorption efficiency of the CNT component itself exhibits a declining trend as the doping concentration increases. This phenomenon is primarily attributed to the convex curvature of the CNTs, which restricts the effective contact area and weakens the adsorption potential, alongside the steric hindrance effects arising from local filler agglomeration at higher concentrations. Furthermore, surface chemical properties exert a significant regulatory influence on adsorption; a strongly hydrophilic modified surface (λ = 1.5) achieved an adsorption capacity approximately 98% higher than the baseline condition—an improvement that exceeds the gains provided by purely physical volume expansion. This research elucidates the synergistic mechanism between physical architecture and surface chemical modification in the adsorption process, suggesting that while the physical architecture determines the abundance of potential adsorption sites, the surface chemistry governs the actual efficiency of site utilization. These findings provide critical theoretical insights for the future design of composite aerogel materials that balance structural stability with superior adsorption performance. Full article

To investigate the effects of incorporating nanomaterials—carbon nanotubes (CNTs) and graphene oxide (GO)—on the axial compressive mechanical properties of alkali-activated recycled aggregate concrete (AARAC) after high-temperature exposure, this study designed 51 sets of specimens with recycled coarse aggregate replacement rate, nanomaterial content, and temperature as the main parameters. Compression tests were conducted to analyze the failure mode and strength variation in AARAC specimens after heating. In addition, microscopic tests, including X-ray diffraction, scanning electron microscopy, and computed tomography (CT scanning), were performed to analyze the microstructural characteristics of the post-heated AARAC specimens. The results indicate that as the replacement rate of recycled coarse aggregate increased from 0% to 100%, the residual compressive strength after exposure to 600 °C decreased from 33.6 MPa to 19 MPa. When 0.1 wt% of CNTs is added, the compressive strength of AARAC after exposure to a high temperature of 600 °C increases by approximately 30.4% compared to that of AARAC without nanomaterial addition. When 0.1 wt% of CNTs and 0.05 wt% of GO are added, the compressive strength after exposure to a high temperature of 600 °C increases by approximately 44.3%, while the size of scattered fragments upon failure increased, and the failure mode appeared more complete. Microscopic test results indicate that the high-temperature treatment did not cause significant changes in the main phase composition of AARAC. The synergistic effect of the nanomaterials CNTs and GO can fully utilize their functions as nucleation sites, pore fillers, and crack bridging agents. By strengthening the Interfacial Transition Zone between the recycled coarse aggregate and the cement paste, refining the Matrix Pore Structure, dispersing local thermal stress, and suppressing the propagation of high-temperature cracks, the mechanical properties of AARAC after high-temperature exposure can be effectively maintained. Full article

Background and objectives: Occupational and environmental inhalation exposures, including high-aspect-ratio carbon nanotubes, can trigger pulmonary fibrosis (PF). The relationship between exposure-specific fibrogenic pathways (granulomatous inflammation versus diffuse epithelial injury) and lung microbiome dysbiosis remains incompletely understood. We therefore compared lung microbiome alterations in rat PF models induced by multi-walled carbon nanotubes (MWCNTs) and bleomycin. Materials and Methods: Female Wistar rats received a single intratracheal instillation of vehicle, MWCNTs (750 μg/rat), or bleomycin (1 mg/rat). At day 28, fibrosis and inflammation were evaluated by histopathology and bronchoalveolar lavage fluid (BALF) profiling. Lung microbial communities were characterized by 16S rRNA gene sequencing (V3–V4). Seventeen lung samples passed stringent quality control and were analyzed (control n = 5; bleomycin n = 7; MWCNT n = 5). Results: Both agents induced PF with increased profibrotic signaling, but with distinct pathological signatures: MWCNTs produced localized granulomatous lesions and a robust neutrophilic response (25% of BALF cells), whereas bleomycin caused diffuse interstitial remodeling. Bleomycin increased microbial richness (alpha diversity; p < 0.05) and significantly shifted community structure (beta diversity; p < 0.05), while MWCNT exposure showed comparatively limited changes in global diversity. The relative abundance of Pseudogracilibacillus (including P. marinus) was higher in the bleomycin group than in controls, whereas Facklamia tabacinasalis and Corynebacterium maris were more abundant in the MWCNT group. Across samples, Proteobacteria abundance was inversely correlated with BALF TGF-β, MCP-1, and neutrophil proportion. At the species level, Pseudogracilibacillus marinus was positively correlated with BALF TGF-β, while Facklamia tabacinasalis and Corynebacterium maris were positively correlated with MCP-1, CINC-3, and neutrophil proportion (Spearman; p < 0.05). Conclusions: Mechanistically distinct fibrogenic exposures generate exposure-linked lung microbiome signatures that track with host inflammatory and profibrotic responses. These signatures may support biomarker development for environmentally and occupationally relevant PF and motivate longitudinal and functional studies to clarify causality. Full article

This study investigates the electrostatic and electrochemical behavior of polyaniline (PANI) and its composite with amine-functionalized multi-walled carbon nanotubes (PANI/MWCNT–NH₂) to elucidate the mechanisms governing ammonia (NH₃) sensing. High-resolution atomic force microscopy (AFM) coupled with electrostatic force microscopy (EFM) demonstrates that pristine PANI forms granular macroaggregates with localized charge distribution, whereas MWCNT incorporation promotes worm-like percolative networks that enhance charge delocalization and conductivity. Electrochemical characterization by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) corroborates these nanoscale observations, revealing significantly improved interfacial electron transfer kinetics in the composite. Upon exposure to NH₃, pristine PANI undergoes rapid de-doping and nonlinear signal suppression, while the composite exhibits a more progressive electrochemical modulation. Overall, the results demonstrate that NH₃ sensing in PANI-based films is governed not solely by electroactive material content but by the interplay between nanoscale morphology, electrostatic heterogeneity, and charge transport topology. The nanotube-mediated formation of delocalized and percolative conductive pathways provides structural and electrochemical robustness, enabling tunable, high-sensitivity operation suitable for next-generation, low-power ammonia sensing platforms. Full article

To mitigate the interlayer defects and weak interfacial adhesion inherent in FFF-printed parts, thereby facilitating subsequent supercritical foaming applications, a microwave-assisted interlayer healing strategy is developed for FFF-printed, supercritical CO₂-foamed thermoplastic polyurethane (TPU) by incorporating aminated helical multi-walled carbon nanotubes (AS-MWCNTs). Owing to their unique helical morphology, AS-MWCNTs exhibit enhanced microwave absorption and localized heating capability, enabling selective thermal activation at interlayer regions within the foamed architecture. Microwave irradiation induces localized softening of the TPU matrix and promotes polymer chain mobility and interdiffusion across layer interfaces, while preserving the cellular morphology and bulk foamed structure. By optimizing AS-MWCNT loading, substantial improvements in interlayer bonding strength, energy absorption, and overall mechanical performance are achieved. This work provides an effective strategy to restore interlayer integrity in supercritical CO₂-foamed, additive manufactured elastomers and offers insights into the design of microwave-responsive, self-healing cellular materials. Full article

For the first time, hybrid nanocomposites based on poly(2,5-dichloro-3,6-bis(phenylamino)-p-benzoquinone) (PCPAB) and multi-walled carbon nanotubes (MWCNTs) were obtained and the influence of the preparation method on their structure and functional properties was demonstrated. The nanocomposites were obtained both by ultrasonic mixing of PCPAB and MWCNTs, and via in situ oxidative polymerization of CPAB in the presence of MWCNTs or MWCNTs with the addition of ZnO. The formation of hybrid nanocomposites occurs due to non-covalent interaction (π-stacking) between the graphene structures of the MWCNT surface and the phenyl rings of PCPAB. It was found that during the in situ oxidative polymerization of CPAB in the presence of MWCNTs, the growth of polymer chains occurred in close proximity to the filler surface, which led to the formation of a polymer coating. ZnO particles, localized on MWCNTs, on the one hand, prevent their aggregation, and on the other hand, create additional polymerization reaction centers due to the coordination of the Zn-O bond at the H and O atoms of the monomer. An increase in the concentration of reaction centers as a result led to a 2–2.5-fold reduction in the induction polymerization period. According to SEM data, in this case, a more ordered and denser polymer layer is formed due to intermolecular complexation between the main and side chains of the growing polymer with the participation of Zn²⁺ ions formed as a result of the transformation of ZnO to ZnCl₂ in the acidic reaction medium of polymerization. The results of the study of the frequency dependences of conductivity indicate a hopping mechanism of conductivity of nanocomposites. The electrical conductivity of nanocomposites depends on their production method and the MWCNT content and varies between 0.5 and 1.1 S∙cm⁻¹, which is 6–12 times higher than the conductivity of the original polymer. Thermogravimetric analysis revealed that the nanocomposites exhibit enhanced thermal stability compared to PCPAB. The best results were shown by nanocomposites with a higher content of MWCNTs, for which the residual mass at 450 °C was 51–53%. Full article

Interfacial coupling between CoFe₂O₄ (CFO) nanoparticles and oxidatively functionalized multi-walled carbon nanotubes (MWCNTs) enables controlled modulation of structural, optical, and spin dynamic properties in CFO–MWCNT nanocomposites. The solvothermal synthesis promotes nucleation of CFO on –COOH/–OH functional groups, ensuring uniform anchoring along the nanotube surface. X-ray diffraction confirms a cubic spinel phase with lattice expansion from 8.385 Å to 8.410 Å and crystallite growth from 18 nm to 25 nm, reflecting strain transfer and partial nanoparticle coalescence at the carbon interface. The observed bandgap narrowing from 2.72 eV to 2.50 eV, confirmed via Tauc plot analysis, is attributed to localized defect states induced by charge delocalization and orbital hybridization at the interface of the CFO–MWCNT boundary. DC magnetometry reveals a reduction in saturation magnetization from 46 emu/g to 35 emu/g due to diamagnetic dilution and interfacial spin canting, while coercivity decreases from 852 Oe to 841 Oe, indicating modified pinning and domain-wall dynamics associated with exchange-coupled interfaces. Ferromagnetic resonance measurements show a resonance field shift from 3495 G to 3500 G and an increase in the Landé g-factor from 1.97 to 2.00, signifying altered spin–orbit coupling and enhanced local magnetic perturbations. The spin–lattice relaxation time increases from 1.41 ns to 1.59 ns, demonstrating suppressed phonon-mediated relaxation and improved spin coherence across the hybrid network. Spin density rises from 3.72 × 10²² to 4.58 × 10²² spins/g, confirming an increase in unpaired electrons generated by orbital asymmetry at the interface. The anisotropy field and effective magnetocrystalline anisotropy constant exhibit pronounced modulation, evidencing strengthened exchange stiffness and altered Co²⁺/Fe³⁺ superexchange pathways. These results establish CFO-MWCNT nanocomposites as tuneable platforms for spintronic logic elements, high-frequency microwave attenuation, and magneto-optical device architectures. Full article

A flexible piezoresistive material based on vulcanized natural rubber (VNR) and multiwalled carbon nanotubes (MWCNTs) was developed and systematically investigated for strain sensing applications. The nanocomposites were prepared by melting and vulcanizing MWCNT, while keeping the rubber composition constant to isolate the effect of the conductive nanofiller. By scanning electron microscopy, morphological analyses indicated that MWCNTs were dispersed throughout the rubber matrix, with localized agglomerations becoming more evident at higher loadings. In mechanical tests, MWCNT incorporation increases the tensile strength of VNR, increasing the stress at break from 8.84 MPa for neat VNR to approximately 10.5 MPa at low MWCNT loadings. According to the electrical characterization, VNR-MWCNT nanocomposite exhibits a strong insulator–conductor transition, with the electrical percolation threshold occurring between 2 and 4 phr. The dc electrical conductivity increased sharply from values on the order of 10⁻¹⁴ S·m⁻¹ for neat VNR to approximately 10⁻³ S·m⁻¹ for nanocomposites containing 7 phr of MWCNT. Impedance spectroscopy revealed frequency-independent conductivity plateaus above the percolation threshold, indicating continuous conductive pathways, while dielectric analysis revealed strong interfacial polarization effects at the MWCNT–VNR interfaces. The piezoresistive response of samples containing MWCNT exhibited a stable, reversible, and nearly linear response under cyclic tensile deformation (10% strain). VNR/MWCNT nanocomposites demonstrate mechanical compliance and tunable electrical sensitivity, making them promising candidates for flexible and low-cost piezoresistive sensors. Full article

Herein, we propose a simple and cost-effective method for fabricating moderate-sensitivity surface-enhanced Raman scattering (SERS) substrates using Cu-plasma polymer fluorocarbon (Cu-PPFC) nanocomposite films fabricated through RF sputtering. The use of a composite target composed of carbon nanotube (CNT), Cu, and polytetrafluoroethylene (PTFE) powders (5:60–80:35–15 wt%) offers the advantage of the simple fabrication of moderate-sensitivity SERS substrates with a single cathode compared to co-sputtering. X-ray photoelectron spectroscopy (XPS) revealed that the film surface was partially composed of metallic Cu with Cu-F bonds and Cu–O bonds, confirming the coexistence of the conducting and plasmon-active domains. UV-VIS spectroscopy revealed a distinct absorption peak at approximately 680 nm, indicating the excitation of localized surface plasmon resonances in the Cu nanoclusters embedded in the plasma polymer fluorocarbon (PPFC) matrix. Atomic force microscopy and grazing incidence small-angle X-ray scattering analyses confirmed that the Cu nanoparticles were uniformly distributed with interparticle distances of 20–35 nm. The Cu-PPFC nanocomposite film with the highest Cu content (80 wt%) exhibited a Raman enhancement factor of 2.18 × 10⁴ for rhodamine 6G, demonstrating its potential as a moderate-sensitivity SERS substrate. Finite-difference time-domain (FDTD) simulations confirmed the strong electromagnetic field localization at the Cu-Cu nanogaps separated by the PPFC matrix, corroborating the experimentally observed SERS enhancement. These results suggest that a Cu-PPFC nanocomposite film, easily fabricated using a composite target, provides an efficient and scalable route for fabricating reproducible, inexpensive, and moderate-sensitivity SERS substrates suitable for practical sensing applications. Full article

The development of multifunctional polymer composites capable of both heat conduction and latent heat storage is of great interest for advanced thermal management applications. In this work, thermoplastic polyurethane (TPU) nanocomposites containing microencapsulated paraffin-based phase change materials (PCMs) and multi-walled carbon nanotubes (MWCNTs) were systematically investigated. The microstructure, thermal stability, specific heat capacity, thermal diffusivity and conductivity of these composites were analyzed as a function of the PCM and MWCNTs content. SEM observations revealed the homogeneous dispersion of PCM microcapsules and the presence of localized MWCNT aggregates in PCM-rich domains. Thermal diffusivity measurements indicated a monotonic decrease with increasing temperature for all compositions, from 0.097 mm²·s⁻¹ at 5 °C to 0.091 mm²·s⁻¹ at 25 °C for neat TPU, and from 0.186 mm²·s⁻¹ to 0.173 mm²·s⁻¹ for TPU with 5 vol.% MWCNTs. Distinct non-linear behavior was observed around 25 °C, i.e., in correspondence to the paraffin melting, where the apparent diffusivity temporarily decreased due to latent heat absorption. The trend of the thermal conductivity (λ) was determined by the competing effects of PCM and MWCNTs: PCM addition reduced λ at 25 °C from 0.162 W·m⁻¹·K⁻¹ (neat TPU) to 0.128 W·m⁻¹·K⁻¹ at 30 vol.% PCM, whereas the incorporation of 5 vol.% of MWCNTs increased λ up to 0.309 W·m⁻¹·K⁻¹. In PCM-containing nanocomposites, MWCNT networks efficiently bridged the polymer–microcapsule interfaces, creating continuous conductive pathways that mitigated the insulating effect of the encapsulated paraffin and ensured stable heat transfer even across the solid–liquid transition. A one-dimensional transient heat-transfer model confirmed that increasing the matrix thermal conductivity accelerates the melting of the PCM, improving the dynamic thermal buffering capacity of these materials. Therefore, these results underlined the potential of TPU/MWCNT/PCM composites as versatile materials for applications requiring both rapid heat dissipation and effective thermal management. Full article

In the present study, molecular dynamics simulations with three interatomic potentials (Polymer Consistent Force Field, Adaptive Intermolecular Reactive Empirical Bond Order, and Tersoff) are employed to investigate strain-dependent interfacial thermal resistance across one-dimensional to two-dimensional junctions. Carbon nanotube–graphene junctions exhibit exceptionally low interfacial resistances (1.69–2.37 × 10⁻¹⁰ K·m²/W at 300 K)—two to three orders of magnitude lower than conventional metal–dielectric interfaces. Strain-dependent behavior is highly potential-dependent, with different potentials showing inverse, positive, or minimal strain sensitivity. Local phonon density of states analysis with Tersoff reveals that strain-induced spectral redistribution in graphene toward lower frequencies enhances phonon coupling with carbon nanotube modes. Temperature significantly affects resistance, with 37–59% increases at 10 K compared to 300 K due to long-wavelength phonon scattering. Boron nitride nanotube–hexagonal boron nitride nanosheet junctions exhibit 60% higher resistance (3.2 × 10⁻¹⁰ K·m²/W) with temperature-dependent strain behavior and spacing-insensitive performance. Interfacial resistance is independent of pillar height, confirming junction-dominated transport. The discovery of exceptionally low interfacial resistances and material-specific strain responses enables the engineering of thermally switchable devices and mechanically robust thermal pathways. These findings directly address critical challenges in next-generation flexible electronics where devices must simultaneously manage high heat fluxes while maintaining thermal performance under repeated mechanical deformation. Full article

Electron transport in carbon nanotubes (CNTs) is highly sensitive to interactions with their local environment, making them promising candidates for sensing applications. Specifically, this could allow detection of electrochemically and optically inert compounds that typically require complex and expensive analytical techniques. In this study, we examine how single-walled carbon nanotubes (SWCNTs) respond to perfluorooctanoic acid (PFOA), a common per- and polyfluoroalkyl substance (PFAS). To improve sensitivity, we employ a single/few-CNT device setup where a small number of SWCNTs were aligned across nanogaps between gold electrodes with the dielectrophoresis method. This structure addresses the challenges of large CNT networks, such as inter-CNT interactions, drift, and degradation, resulting in improved stability for practical applications. Results showed that device resistance drops as a function of PFOA concentrations. Additionally, positive gate voltage enhances sensitivity by attracting negatively charged PFOA molecules to the SWCNT surface. Specifically, we report that the sensitivity increases by nearly an order of magnitude under a 0.3 V gate bias. Impedance spectroscopy reveals distinct amplitude and phase signatures, enabling selective detection of PFOA among different analytes. Applying gate voltage further enhances sensor selectivity, highlighting the potential of gated SWCNT devices for accurate and selective environmental monitoring. The device demonstrates promising performance as a robust platform for creating single/few-CNT nanosensors for detecting electrochemically and optically inert substances like PFAS molecules. Full article