Search Results (15)

In this study, the dyeing kinetics of polyamide fabrics with acid dyes, such as Telon Blue M2R, under both conventional and microwave-assisted heating conditions were comprehensively investigated. While the conventional dyeing reaction was completed in 30 min, microwave-assisted dyeing was performed in the microwave device for 10 min. Dyeing kinetics were investigated as a function of reaction time, reaction concentration and dyeing temperatures. The K/S values (color depth) of the dyed fabrics were correlated with the concentration. A significant reduction in the dyeing process time for polyamide fabric was observed with microwave heating compared to the conventional method. Kinetic analysis revealed that the Pseudo-Second-Order (PSO) kinetic model provides a better fit to the experimental data on the diffusion process of acid dye in polyamide fabrics, as evidenced by higher correlation coefficients (R²) compared to the Pseudo-First-Order (PFO) model. The activation energy of the reaction in dyeing was found to be 63.27 kJ/mol, and the Arrhenius constant was determined as 7.20 × 10¹⁰ L/g·min in conventional media and 18.70 × 10¹⁰ L/g·min in microwave media. The Arrhenius factor in the microwave medium was more than two times higher than in the conventional media. Full article

Thermoplastic carbon fiber-reinforced polymer (CFRP) composites possess the intrinsic capability to heal delamination and matrix cracks via thermal re-melting. However, under impact loading, they are prone to severe fiber fracture, which significantly compromises their repairability. To address this, this study introduced polytetrafluoroethylene (PTFE) films as pre-set interlaminar defects within continuous carbon fiber-reinforced polyamide 6 (CF/PA6) thermoplastic cross-ply laminates. Low-velocity impact tests were conducted at varying energy levels to comparatively investigate the impact response and damage mechanisms of the CFRPs with and without embedded defects. Experimental results indicate that the embedded interlaminar defects triggered a transition in the failure mode of the CFRP from brittle fracture to progressive damage behavior. Compared to the baseline laminates, the specimens with embedded defects maintained higher flexural stiffness under low-energy impact. Furthermore, they effectively reduced the extent of fiber breakage by dissipating impact kinetic energy through extensive delamination, interlaminar frictional sliding, and plastic micro-deformation. These findings verify the feasibility of achieving macroscopic pseudo-ductility through interlaminar microstructural tailoring. This research provides an experimental basis and methodological support for the pseudo-ductile design of thermoplastic composites. Full article

The growing interest in sustainable additive manufacturing has driven research into customized biocomposite filaments reinforced with natural fibers. This study evaluates the influence of flax fiber content (5–15 wt%) on the thermal, rheological, morphological, and mechanical properties of fully bio-based polyamide PA10.10 filaments intended for fused deposition modeling (FDM). Filaments containing up to 15 wt% flax fibers were produced using both conventional single-screw extrusion and the METEOR^® elongational mixer to compare shear- and elongation-dominated dispersive mechanisms. Increasing flax loading enhanced stiffness (up to +84% tensile modulus at 15 wt%) but also significantly increased porosity, particularly in METEOR-processed materials, leading to reduced strength and intrinsic viscosity. Microscopy confirmed fiber shortening during compounding and revealed porosity arising from moisture release and insufficient fiber wetting. Rheological analysis showed the onset of a pseudo-percolated fiber network from 10 wt%, while excessive porosity at higher loadings impeded melt flow and printability. Based on the combined evaluation of the mechanical performance, dimensional stability, and processability, a 5 wt% flax formulation was identified as the optimal compromise for FDM. A functional automotive demonstrator (Fiat 500 dashboard fascia) was successfully printed using optimized FDM parameters (nozzle 240 °C, bed 75 °C, speed 20 mm s⁻¹, 0.6 mm nozzle, 0.20 mm layer height, and 100% infill). The part exhibited controlled shrinkage and limited warpage (maximum 1.8 mm across a 165 × 180 × 45 mm geometry with a 3 mm wall thickness). Dimensional accuracy remained within ±0.7 mm relative to the CAD geometry. These results confirm the suitability of PA10.10/flax biocomposites for sustainable, lightweight automotive components and provide key structure–processing–property relationships supporting the development of next-generation bio-based FDM feedstocks. Full article

Efficient recycling of polyamide 6 (PA6) requires selective depolymerization routes that recover monomers under moderate conditions. This study investigates microwave-assisted acid hydrolysis of four PA6 waste streams, two oligomer-rich residues (WS-13, WS-24), an industrial fiber (C-fiber), and a commercial resin (C-resin) to elucidate degradation kinetics, activation energies, and product yields. Thermogravimetric analysis revealed multi-step solid-state decomposition, while microwave hydrolysis (125–200 °C, 15–60 min, 400 W) demonstrated strong dependence on acid type. HCl achieved complete conversion, whereas phosphoric and formic acids exceeded 95%. Kinetic analysis under H₃PO₄ followed pseudo-first-order behavior, with rate constants (0.015–0.141 min⁻¹ at 200 °C) and activation energies reflecting feedstock structure: 53.1 kJ mol⁻¹ (WS-13), 56.5 kJ mol⁻¹ (WS-24), 87.1 kJ mol⁻¹ (C-resin), and 99.9 kJ mol⁻¹ (C-fiber). Monomer yields varied by substrate: WS-13 achieved 62.4% at 200 °C and 45 min (ACA 46%, CPL 16%), WS-24 yielded 62.0% (primarily ACA), C-fiber reached 69.7% (ACA-dominant), and C-resin produced 53.8%. These results show that oligomer-rich wastes are kinetically favored for rapid hydrolysis at lower energy cost, while C-fiber maximizes aminocaproic acid recovery. Overall, microwave-assisted hydrolysis provides a selective, energy-efficient pathway for PA6 circularity, offering design parameters for reactor operation and process optimization. Full article

The biaxially-oriented PA56/512 has excellent mechanical strength, extensibility and water–oxygen barrier properties and has broad application prospects in green packaging, lithium battery diaphragm and medical equipment materials. The correlation between the aggregation structure evolution and macroscopic comprehensive properties of copolymer PA56/512 under biaxial stretching has been demonstrated in this work. The structure of the random copolymerization sequence was characterized by ¹³C Nuclear magnetic resonance (NMR). The typical isodimorphism behavior of the co-crystallization system of PA56/512 and its BOPA-56/512 films was revealed by differential scanning calorimetry (DSC) and X-ray diffraction (XRD) tests. And the aggregation structure, including the hydrogen bond arrangement, crystal structure and crystal morphology of PA56/512 before and after biaxial stretching, was investigated by XRD, Fourier-transform infrared spectroscopy (FTIR) and polarized optical microscopy (POM) tests. Furthermore, the effect of the biaxially-oriented stretching process on the mechanical properties of PA56/512 has been demonstrated. In addition, a deep insight into the influence of the structure on the crystallization process and physical–mechanical performance has been presented. The lowest melting point at a 512 content of 60 mol% is regarded as a “eutectic” point of the isodimorphism system. Due to the high disorder of the structural units in the polymer chain, the transition degree of the folded chain (gauche conformation) is relatively lowest when it is straightened to form an extended chain (trans conformation) during biaxially-oriented stretching, and part of the folded chain can be retained. This explains why biaxially stretched PA56/512 has high strength, outstanding toughness and excellent barrier properties at the pseudo-eutectic point. In this study, using the unique multi-scale aggregation structure characteristics of a heterohomodymite polyamide at the pseudo-eutectic point, combined with the new material design scheme and the idea of biaxial-stretching processing, a new idea for customized design of high-performance multifunctional polyamide synthetic materials is provided. Full article

Bio-based polyamide 10.10 (PA 10.10) has excellent properties compared to other bio-based polymers such as polylactic acid (PLA) or polyhydroxyalkanoates (PHAs) and is therefore used in more technical applications where higher strength is required. For foam and filament extrusion, a good balance between strength and stiffness of the polymer is needed. Therefore, two commercial chain-extenders (Joncryl^® ADR types) with different epoxy functionalities are used to modify the melt properties of PA 10.10. The chain-extenders are used in a concentration range up to 1.25 wt.%. The range of glass transition temperature widens with increasing Joncryl^® content, and the apparent activation energy shows a maximum at a concentration of 0.5 wt.%. Furthermore, the melting temperatures are constant and the crystallinity decreases with increasing chain-extender content due to the formation of branches. During the second heating run, a bimodal melting peak appeared, consisting of $\alpha$-triclinic and pseudo $\gamma$-hexagonal crystals. The weight average molar masses (M_w) measured by gel permeation chromatography (GPC) increased linearly with increasing ADR 4400 content. In contrast, the compounds containing ADR 4468 show a maximum at 0.5 wt.% and it begins to decrease thereafter. The rheological data show an increase in viscosity with increasing chain-extender content due to branch formation. ATR spectra of the compounds show a decrease at the wavelength of the primary (3301 cm⁻¹) and secondary (1634 cm⁻¹) (-NH stretching in PA 10.10) amine, indicating that chain-extension, e.g., branching, takes place during compounding. Full article

Sustainable serpentine/polyamide nanocomposite (SP/PAM) was fabricated using malicious mining (serpentine chrysotile, SP Ctl) and industrial (polyamide, PA6) wastes via the electro-spinning technique. Before fabrication, the fibrous nature of Ctl was demolished through intensive grinding into nano-fractions. The successful impregnation of Ctl within PA6 via the electro-spinning technique at fixed ratios of precursor raw materials in the dissolving agent (7.5/92.5% SP/PA wt/wt solid/solid) created an internal network structure within the polymer fibers by molecular self-assembly. SP/PAM showcased its prowess in tackling the remediation of diverse dyes and Fe(III) from synthetic solutions in a batch system. Based on correlation coefficient outcomes (R² ≈ 0.999), the pseudo-second-order equation justified the sorption data in an adequate way for all contaminants. In addition, intra-particle diffusion was not the only driving factor in the sorption process. Similarly, the Langmuir equation with maximum removal capacity (qmax) 5.97, 4.33, and 5.36 mg/g for MO, MB, and Fe(Ⅲ), respectively, defined the sorption data better than Freundlich. Full article

In this work, we investigated the effect of various adsorption parameters (solution pH, temperature, contact time, and the presence of phosphate and nitrate ions) on the adsorption of Reactive Red 120 (RR120) dye by Polyamide Nylon 6 (PN6) microplastics (MPs). Maximum uptake was achieved at pH 2.0, and the temperature rise from 295 to 313 K resulted in the decrease of the RR120 sorption by PN6. Equilibrium was achieved after 7 h, and the adsorption kinetic data obeyed the pseudo-second-order kinetic model. The experimental adsorption data were better fitted by the Langmuir isotherm model, and the q_m was found to be 3.96 mg/g at pH 2.0 and 295 K. Thermodynamic studies pointed out that the adsorption was spontaneous and exothermic, with decreasing entropy at the solution/solid interface. Future work will focus on the effect of aging on the adsorptive properties of PN6 toward RR120 dye. Full article

The interface of hybrid carbon/E-glass fibres composite is interlayered with Xantu.layr^® polyamide 6,6 nanofibre veil to localise cracking to promote a gradual failure. The pseudo-ductile response of these novel stacking sequences examined under quasi-static three-point bending show a change to the failure mechanism. The change in failure mechanism due to the interfacial toughening is examined via SEM micrographs. The incorporation of veil toughening led to a change in the dominant failure mechanism, resulting in fibre yielding by localised kinking and reduced instances of buckling failure. In alternated carbon and glass fibre samples with glass fibre undertaking compression, a pseudo-ductile response with veil interlayering was observed. The localisation of the fibre failure, due to the inclusion of the veil, resulted in kink band formations which were found to be predictable in previous micro buckling models. The localisation of failure by the veil interlayer resulted in a pseudo-ductile response increasing the strain before failure by 24% compared with control samples. Full article

Surface-initiated photopolymerization has been run to synthesize a hydrogel with ZnO particles distributed uniformly along its structure, which has been loaded onto a polyamide fabric. Three samples have been obtained at different concentrations of zinc nitrate (10% (sample PA10); 20% (sample PA20) and 30% (sample PA30) of the weight of the fabric, respectively)) and subjected to gravimetric analysis, scanning electron microscopy and transmission electron microscopy. The effect of the adsorption parameters of the composite material on the removal Drimaren Rot K-7B dye from water has been studied. The Freundlich isotherm describes this process better than the Langmuir isotherm. As the results of the adsorption kinetics show, the process fits well with a pseudo-second-order equation and depends both on the boundary layer and on the structure of the adsorbent itself. The thermodynamic parameters have demonstrated that the process is endothermic and physical. When exposed to ultraviolet light, the discoloration of the dye solution accelerates due to the photocatalytic properties of the composite materials. The addition of H₂O₂ also speeds up further the process, while the reuse of the materials slows it down, gradually changing the kinetic parameters. The reaction has been attributed to first-order kinetic model, when the active centers of the materials and the number of oxidative radicals formed are numerous and to the second-order kinetic model at a lower reaction activity. Moreover, 52% decolorization of the dye solution (50 mg L⁻¹) in the dark was achieved from composite material PA 30 (13.3 g L⁻¹) in 120 min and 89% under UV light irradiation. The H₂O₂ addition (0.14 mmol L⁻¹) enhanced it up to 98%. In the second and third use of the photocatalyst, the dye removal decreased to 80% and 60%. Composite material PA30 exhibits antibacterial activity against Gram-negative bacteria E. coli, being most effective at eliminating Gram-positive bacteria S. aureus. Full article

Mixed cadmium tellurides–cadmium sulfide thin layers were formed on the polyamide PA 6. Monotelluropentathionic acid (H₂TeS₄O₆) was used as a precursor of tellurium and sulfur. A low-temperature, nontoxic, and cost-effective SILAR method was applied. Cadmium telluride (CdTe) and sulfide (CdS) layers were formed through the consecutive reactions of sorbed/diffused chalcogens species from telluropentathionate anion (TeS₄O₆²⁻) with functional groups of polyamide and alkaline cadmium sulfate. The pseudo-second-order rate and Elovich kinetic models were the best fit to quantify an uptake of chalcogens and cadmium on PA 6. The effects of chalcogens and Cd on the structure and optical properties of PA 6 were characterized using UV-Vis and IR spectra. The clear changes of these properties depended on the concentration and exposure time in the precursor solutions. Fourier transform infrared spectroscopy and ultraviolet-visible spectroscopy were applied in order to evaluate the effect of the chalcogen species on the changes in structure of polyamide 6 films, depending on the exposure time in the solution of the chalcogens precursor and its concentration. The optical bandgap energy of the formed layers was found to be in the order of 1.52–2.36 eV. Studies by scanning electron microscopy and atomic force microscopy reveal that the diameter of the average grain is approximately 30 nm. The grains are conical in shape and unevenly distributed all over the surface of the substrate. Full article

Using polyacrylic resin followed by the substitution reaction with 6-aminohexyl hydroxamic acid, poly(6-acryloylamino-hexyl hydroxamic acid) resin (PAMHA) was successfully synthesized. PAMHA, a spherical resin with the particle size of 0.4 mm, is a novel polyamide hydroxamic acid chelating resin containing acylamino and hydroxamic acid functional groups. A series of influences (pH, contact time, temperature, and the initial concentrations of rare earth ions) were investigated to determine the adsorption properties. The adsorption capacity for La(III), Ce(III), and Y(III) ions were 1.030, 0.962, and 1.450 mmol·g⁻¹, respectively. Thermodynamic and kinetic studies were also carried out to show that the uptake of rare earth ions onto PAMHA fitted well the pseudo-second-order model and Langmuir isotherm, and the adsorption process was spontaneous endothermic. In addition, desorption of rare earth ions was achieved by using 2 mol·L⁻¹ HNO₃ and desorption efficiencies for La(III), Ce(III), and Y(III) ions were 98.4, 99.1, and 98.8%, respectively. Properties of PAMHA resin were characterized by scanning electron microscope (SEM), Fourier transform infrared spectrometry (FTIR), and X-ray photoelectron spectrometer (XPS). The results showed that there was coordination between the rare earth ions with PAMHA and rare metal ions were chemically adsorbed on the surface of the PAMHA. Full article

Nowadays, polymers used in technical applications are still obtained from petrochemicals, despite the more critical reviews from society. In this work, novel nanodielectrics based on renewable resources were developed. For this purpose, poly(2-oxazoline)s (POx), which can be referred to as pseudo-polyamides, were synthesized from renewable resources and compared with commercially available Nylon 12, which is derived from petrochemicals. The monomers 2-nonyl-2-oxazoline and 2-dec-9′-enyl-2-oxazoline were synthesized from coconut oil and castor oil in solvent-free syntheses according to the Henkel Patent; the corresponding copoly(2-oxazoline)s were synthesized in an energy-efficient fashion in microwave reactors under autoclave conditions. Both types of polyamides (two variations: POx and Nylon 12) were filled with inorganic nanoparticles (four variations: no filler, submicro-scaled BN, nano- and micro-scaled AlN as well as a mixture of nano- and micro-scaled AlN and submicro-scaled BN) and/or expanding monomers, namely spiroorthoesters (three variations: 0, 15, and 30 wt.-%), yielding a 2 × 4 × 3 = 24-membered material library. All polymers were crosslinked according to a newly developed thermally-initiated dual/bi-stage curing system. Intense physicochemical and dielectric characterization revealed that the relative volume expansion was in the range of 0.46 to 2.48 vol.-% for the Nylon 12 samples and in the range of 1.39 to 7.69 vol.-% for the POx samples. Hence, the formation micro-cracks or micro-voids during curing is significantly reduced. The dielectric measurements show competitive dielectric behavior of the “green” POx samples in comparison with the fossil-based Nylon 12 samples at a frequency of 40 Hz. Full article

Polyamide 6 (PA6)/poly(vinylidene fluoride) (PVDF) blend-based nanocomposites were successfully prepared using a twin screw extruder. Carbon nanotube (CNT) and organo-montmorillonite (30B) were used individually and simultaneously as reinforcing nanofillers for the immiscible PA6/PVDF blend. Scanning electron micrographs showed that adding 30B reduced the dispersed domain size of PVDF in the blend, and CNT played a vital role in the formation of a quasi-co-continuous PA6-PVDF morphology. Transmission electron microscopy observation revealed that both fillers were mainly located in the PA6 matrix phase. X-ray diffraction patterns showed that the presence of 30B facilitated the formation of γ-form PA6 crystals in the composites. Differential scanning calorimetry results indicated that the crystallization temperature of PA6 increased after adding CNT into the blend. The inclusion of 30B retarded PA6 nucleation (γ-form crystals growth) upon crystallization. The Young’s and flexural moduli of the blend increased after adding CNT and/or 30B. 30B exhibited higher enhancing efficiency compared with CNT. The composite with 2 phr 30B exhibited 21% higher Young’s modulus than the blend. Measurements of the rheological properties confirmed the development of a pseudo-network structure in the CNT-loaded composites. Double percolation morphology in the PA6/PVDF blend was achieved with the addition of CNT. Full article

Polyamide fiber has the requirements for antioxidant and antibacterial properties when applied to produce functional textiles for heath care purposes. In this work, three natural flavonoids (baicalin, quercetin, and rutin) were used to simultaneously impart antioxidant and antibacterial functions to polyamide fiber using an adsorption technology. The relations of the chemical structures of flavonoids with their adsorption capability, adsorption mechanisms, and antioxidant and antibacterial activities were discussed. The Langmuir–Nernst adsorption model fitted the adsorption isotherms of the three flavonoids well. The adsorption kinetics of the three flavonoids conformed to the pseudo second-order kinetic model. Quercetin exhibited the highest affinity and adsorption capability, and imparted the highest antioxidant and antibacterial activities to polyamide fiber; and moreover, its antioxidant and antibacterial functions had good washing durability. This study demonstrates that the treatment using natural flavonoids is an effective way to exhance the health care functions of polyamide fiber. Full article