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The use of biodegradable polymers for the production of membranes to be used in wastewater treatment has attracted increasing interest considering the possibility of reducing the risk of second pollution. In this work, porous fibrous membranes based on polylactic acid and polyethylene oxide (PEO) blends were prepared. The solutions were electrospun using two approaches: (i) conventional coaxial electrospinning followed by leaching treatment (double-step, DS); (ii) coaxial wet electrospinning with in situ leaching (single-step, SS). By varying PEO type and processing method it was possible to control membranes structure and porosity. DS leaching treatment lead to surface porosity (i.e. shell leaching), while SS allowed obtaining hollow and porous fibers (i.e. with shell and core leaching). Process, properties and structure relationships of devices were analysed trough rheological, morphological, mechanical and surface characterizations. Furthermore, the influence of the different porous structures on oil sorption capacity and reusability of the membranes was evaluated. Results reveal that different porosities lead to a variation in membranes mechanical performance, in their wettability and, consequently, in their oil spill cleanup capacity. Membranes obtained with SS displayed higher performance in oil removal if compared to the DS ones, due to their hollow structure and higher surface area.

Growing environmental concerns are stimulating researchers to develop more and more efficient materials for environmental remediation. Among them, polymer-based hierarchical structures, attained by properly combining certain starting components and processing techniques, represent an emerging trend in materials science and technology. In this work, graphene oxide (GO) and/or carbon nanotubes (CNTs) were integrated at different loading levels into poly (vinyl fluoride-co-hexafluoropropylene) (PVDF-co-HFP) and then electrospun to construct mats capable of treating water that is contaminated by methylene blue (MB). The materials, fully characterized from a morphological, physicochemical, and mechanical point of view, were proved to serve as membranes for vacuum-assisted dead-end membrane processes, relying on the synergy of two mechanisms, namely, pore sieving and adsorption. In particular, the nanocomposites containing 2 wt % of GO and CNTs gave the best performance, showing high flux (800 L × m−2 h−1) and excellent rejection (99%) and flux recovery ratios (93.3%), along with antifouling properties (irreversible and reversible fouling below 6% and 25%, respectively), and reusability. These outstanding outcomes were ascribed to the particular microstructure employed, which endowed polymeric membranes with high roughness, wettability, and mechanical robustness, these capabilities being imparted by the peculiar self-assembled network of GO and CNTs.

Nuclear energy has significantly promoted the development of human society. However, nuclear pollution caused by nuclear accidents can lead to significant hazards to the environment and human health. As a major radioactive product, radioactive iodine (mainly existing as I−) detection has attracted significant attentions. In this study, zirconium(IV) is used to enhance the oxidation of environmental I− to form I2. Subsequently, the generated I2 oxidizes the chemical chromogenic substrate 3,3′,5,5′-tetramethylbenzidine, which is used for I− detection and realizes an ultralow limit of detection (LoD) of 0.176 nM. The LoD of our method, to the best of our knowledge, is the lowest among those of the available chemical methods for I− detection. Furthermore, our detection method also shows high specificity and reliability, making it a promising technique for detecting I− in practical environments.

We present a fast, one step method to obtain PVA/graphene/chlorhexidine nanofibrous membranes, with a crosslinking gradient along their cross-section. Briefly, polymeric solutions were electrospun onto a heated plate, enabling the in situ crosslinking of PVA macromolecules. Of course, the crosslinking degree of such structures was found to decrease upon the distance from the plate during deposition. The outcomes reveal the crucial role of graphene, capable of promoting heat transfer throughout the entire structure, thus leading to 70-80% crosslinking degrees and preventing delamination issues. Such membranes were compared to untreated and oven thermally treated ones, and a robust relationship between processing, structure and properties was outlined, with a special focus on the release behaviour of such materials, which proved to be tuneable from instantaneous/burst to sustained release (up to 500 hours) by adjusting formulation and preparation technique.

Graphene oxide (GO) and carbon nanotubes (CNTs) were integrated at different mutual ratios into poly(vinyl fluoride-co-hexafluoropropylene) (PVDF-co-HFP) and electrospun to construct mats that were assessed for treating water contaminated by methylene blue (MB) via vacuum-assisted ultrafiltration. The materials were fully characterized from a morphological, physicochemical and mechanical point of view. The results revealed that such materials are suitable for being used as membranes for continuous processes, such as ultrafiltration. In particular, adding 2 wt.% of GO and CNTs gave the best performance, showing extremely high flux (800 L*m− 2*h− 1), excellent rejection (99%) and flux recovery ratios (93.3%), along with antifouling properties (irreversible and reversible fouling below 6% and 25%, respectively), and reusability. These outstanding outcomes were ascribed to the peculiar microstructure achieved, which endowed polymeric membranes with high roughness, wettability, and mechanical robustness.

Excessive fertilization causes ecological problems due to leaching issues. To solve this problem and promote agriculture sustainability an innovative green composite for controlled release fertilizers was produced by adding NPK fertilizer flour to a biodegradable polymer with or without Opuntia Ficus Indica (OFI) particles. Six for- mulations were produced and employed for the fabrication of devices both for compression molding and fused deposition modeling (FDM). Both fillers displayed a good dispersion in the composites, excellent adhesion with the polymeric matrix and effectively acted as reinforcement. The decrease of NPK release rate (up to 30 days) was achieved using whole composites prepared. By appropriately selecting the dimension of the particles, the addition of OFI and the production technique, was possible to modulate the NPK release rate: FDM samples containing fine particles of OFI and NPK displayed the fastest release. Release data were fitted according to Peppas-Korsmeyer model to understand the release mechanism.

Platelet-like and fibrous lignocellulosic fillers were achieved from the leaves of Chamaerops humilis (CHL) and Posidonia oceanica (POL) and used as a hybrid reinforcement for a polylactic acid (PLA) matrix at three different loading levels (from 5 to 20%). The materials were fully characterized from a morphological, physicochemical, mechanical, and dynamic-thermomechanical point of view. When compared to their counterpart containing either CHL or POL only, the resulting hybrid biocomposites showed the highest mechanical properties, with strengthening and stiffening effects respectively up to 120% and 50% higher than those expected from the linear combination of the two, and higher dynamic-mechanical performance, with storage moduli in the rubbery region 10 times higher than those of composites containing solely CHL or POL. Such synergistic efficiency is likely due to the formation of a strong and extensive interphase region, promoted by the balanced effect of morphological features of the hybrid network and physicochemical characteristics of the components. These green materials could find applications as panels for furniture or in the automotive industry. Graphical Abstract

Aim: To develop electrospun mats loaded with Thymus capitatus (L.) essential oil ( ThymEO) and to study their morpho-mechanical and antimicrobial properties. Materials & methods: Poly(lactic acid) (PLA) mats containing ThymEO were prepared by electrospinning. The effect of ThymEO on the morpho-mechanical properties of fibers was assayed by scanning electron microscopy and dynamometer measurements. The antimicrobial activity of ThymEO delivered either in liquid or vapor phase was assessed through killing curves and invert Petri dishes method. The cytotoxicity was also investigated. Results: The mechanical properties were enhanced by integrating ThymEO into PLA. Both liquid and vapors of ThymEO released from mats caused reductions of microbial viable cells. Negligible cytotoxicity was demonstrated. Conclusion: PLA/ ThymEO delivery systems could be suitable for treating microbial infections.

La plastica costituisce la componente più abbondante dei rifiuti in ambiente marino. Le plastiche in mare sono colonizzate da biofilm microbici, denominati plastisfera, che possono comprendere patogeni, specie algali tossiche e invasive e, potenzialmente, organismi in grado di biodeteriorare e degradare le plastiche (Zettler et al. 2013). Lo scopo di questo lavoro è studiare e confrontare le comunità microbiche che colonizzano plastiche biodegradabili e non biodegradabili in ambiente marino. Un esperimento di esposizione di film plastici in ambiente marino portuale è stato allestito per studiare la diversità della plastisfera di alcune plastiche biodegradabili (Mater Bi e PLA-acido polilattico) e non biodegradabili (PET-polietilene tereftalato e HDPE-polietilene ad alta densità). I film plastici sono stati immersi nel bacino La Cala di Palermo in due siti a 2 e 9 metri di profondità e prelevati dopo una esposizione di uno e tre mesi. La biomassa microbica reclutata sulle plastiche è stata stimata al termine dei due periodi di esposizione mediante quantizzazione del DNA totale estratto e conte vitali. La struttura del biofilm è stata osservata attraverso microscopia elettronica a scansione (SEM). La diversità della componente coltivabile dopo tre mesi di esposizione è stata studiata mediante isolamento su terreni di coltura per batteri marini eterotrofi e sequenziamento del gene 16SrRNA. La biodiversità della comunità microbica totale delle plastiche esposte nel sito a maggiore profondità, meno soggette all’influenza della luce solare, è stata analizzata dopo un mese di esposizione mediante analisi dello spaziatore intergenico ribosomale procariotico ITS (Automated Ribsomal Intergenic Spacer Analysis-ARISA) e analisi metagenomica 16SrRNA (Next Generation Sequencing) dopo tre mesi di esposizione. Le potenzialità degradative delle comunità microbiche sono state valutate con analisi gravimetrica. Dopo un’esposizione di 1 e 3 mesi in ambiente marino si osserva un’elevata capacità di colonizzazione microbica su tutti i tipi di plastica ed una tendenza della carica batterica ad aumentare nel tempo. L’osservazione al SEM rivela la presenza di diatomee, strutture filamentose e cellule batteriche sulla superficie delle plastiche. Le plastiche biodegradabili ospitano un maggior numero di batteri coltivabili ed una maggiore biomassa rispetto alle non biodegradabili2. Gli isolati ottenuti dopo tre mesi di esposizione sono stati affiliati ai generi Pseudoalteromonas e Vibrio. L’analisi fingerprinting ARISA sul DNA totale estratto dai biofilm mostra alta beta diversità tra le comunità microbiche di plastiche diverse già dopo un mese di esposizione e maggiori livelli di alfa diversità delle comunità associate al Mater Bi. L’analisi metagenomica condotta sul biofilm adeso a Mater Bi e HDPE (rappresentativi rispettivamente delle plastiche biodegradabili e non biodegradabili) dopo tre mesi di esposizione in mare rivela comunità microbiche in parte differenti e un arricchimento di potenziali patogeni, in particolare delle famiglie Vibrionaceae e Flavobacteriaceae. Sul Mater Bi (bioplastica a base di amido di mais e oli vegetali), che dopo tre mesi di esposizione in mare mostra una perdita di peso del 25% circa rispetto al peso iniziale (Catania et al. 2019), risulta particolarmente abbondante la famiglia Cellvibrionaceae, che comprende membri in grado di degradare polisaccaridi e carboidrati complessi, quali cellulosa, agar, chitina, amido e che potrebbe avere un ruolo nella degradazione del Mater Bi in ambiente marino. I risultati mostrano che tutte le plastiche sono colonizzate da un biofilm microbico che tende ad aumentare in complessità e biomassa nel tempo. Le analisi colturali e molecolari suggeriscono che la struttura del biofilm e la composizione delle comunità microbiche che lo costituiscono sono in parte influenzate dal tipo di substrato/polimero e dal tempo di esposizione e che si differenziano già dopo un mese di esposizione in ambiente marino. La componente coltivabile tuttavia mostra bassi livelli di diversità e non si differenzia tra le plastiche analizzate.

The addition of natural scraps to biodegradable polymers has gained particular interest in recent years, allowing reducing environmental pollution related to traditional plastic. In this work, new composites were fabricated by adding 10% or 20% of Hedysarum coronarium (HC) flour to Poly (lactic acid) (PLA). The two formulations were first produced by twin screw extrusion and the obtained filaments were then employed for the fabrication of composites, either for compression molding (CM) or by fused deposition modeling (FDM), and characterized from a morphological and mechanical point of view. Through FDM it was possible to achieve dense structures with good wettability of the filler that, on the contrary, cannot be obtained by CM. The results indicate that the filler effectively acts as reinforcement, especially for FDM composites. The most remarkable enhancement was found in the flexural properties (+100% of modulus and ultimate strength), followed by tensile resistance and stiffness (+60%) and impact strength (+50%), whereas a moderate loss in tensile deformability was observed, especially at the highest loading. By adding HC to the polymeric matrix, it was possible to obtain a green, high-performance, and cost-effective composite, which could find applications for the fabrication of panels for furniture or the automotive industry.

Graphene is considered the material of the third millennium, due to its extraordinary electronic and mechanical properties, and due to the possibility to modulate its conductivity, flexibility, elasticity, transparency, and biocompatibility by bottom-up approach. The possibility to gather the proper- ties of graphene and graphene oxide with those of functional moieties or nanoparticles is herein reviewed. The synthetic approaches proposed, either covalent or noncovalent, are aimed to tune appropriately graphene’s properties for the realization of materials for advanced uses, such as bio- medical applications, sensors, catalysis, and energy devices. In particular, methods based on covalent linking and noncovalent functionalization by supramo- lecular interaction will be discussed, by elucidating main advantages and drawbacks, focusing on recent papers in developing advanced applications.

Two fibrous fillers were achieved from stalks and leaves of Chamaerops humilis dwarf palm and tested as reinforcing agents for poly(butylene adipate co-terephthalate) (PBAT)-based composites. The influence of filler type and content on the morphomechanical properties of the green composites was assessed. The outcomes of tensile tests pointed out that both fillers are strong candidates to overcome the two main limiting aspects of PBAT, that is, the lack of both stiffness and cost-effectiveness, while preserving its stretchability and environmental sustainability. The remarkable stiffness increments (up to 300%), combined with fair retention of stretchability (33%) and doubled resistance, led to the fabrication of biocomposites with toughness values as high as 20-25 MJ/m(3). These results could be ascribed to the combination of several factors, including the formation of an extensive and robust interphasic region. This latter, ascribed to the chemical affinity between aromatic parts of fillers and matrix, presented different features in the two types of fillers, thus endowing resulting biocomposites with a broad array of mechanical performance, which can be predicted by introducing opportune modifications to Halpin-Tsai model which allow considering the crucial role of interphase.

We report a fast route enabling the multiscale design of nanohybrid structures comprising a 3D fibrous network of polycaprolactone (PCL) wrapped by graphene oxide (GO) sheets onto which carbon nanotube (CNT) brushes are anchored. The method relies on electrospinning PCL solutions onto a suspension of GO and CNTs in ethanol. Self-assembly is due to electrostatic wrapping of GO sheets around PCL fibers and 7C-7C stacking between GO and CNTs. Hierarchical architecture and nanopatterned surface allow gathering the starting properties of PCL, GO and CNTs into lightweight (99% porosity) yet robust (1575% stiffness improvement), amphiphilic monoliths that can remove methylene blue and/or methyl orange from stagnant water with ca.100% efficiency.

The current demand for new antimicrobial systems has stimulated research for the development of poly(lactic acid)/carvacrol (PLA/CAR)-based materials able to hinder the growth and spread of microorganisms. The eco-friendly characteristics of PLA and cytocompatibility make it very promising in the perspective of green chemistry applications as material for food and biomedical employments. The broad-spectrum biological and pharmacological properties of CAR, including antimicrobial activity, make it an interesting bioactive molecule that can be easily compounded with PLA by adopting the same techniques as those commonly used for PLA manufacturing. This review critically discusses the most common methods to incorporate CAR into a PLA matrix and their interference on the morphomechanical properties, release behavior, and antimicrobial activity of systems. The high potential of PLA/CAR materials in terms of chemical-physical and antimicrobial properties can be exploited for the future development of food packaging, coated medical devices, or drug delivery systems.

Fiber-reinforced polymers (FRPs) are low-density, high-performance composite materials, which find important applications in the automotive, aerospace, and energy industry, to only cite a few. With the increasing concerns about sustainability and environment risks, the problem of the recycling of such complex composite systems has been emerging in politics, industry, and academia. The issue is exacerbated by the increased use of FRPs in the automotive industry and by the expected decommissioning of airplanes and wind turbines amounting to thousands of metric tons of composite materials. Currently, the recycling of FRPs downcycles the entire composite to some form of reinforcement material (typically for cements) or degrades the polymer matrix to recover the fibers. Following the principles of sustainability, the reuse and recycling of the whole composite—fiber and polymer—should be promoted. In this review paper, we report on recent research works that achieve the recycling of both the fiber and matrix phase of FRP composites, with the polymer being either directly recovered or converted to value-added monomers and oligomers.

Every day large amounts of fish waste are produced and grossly discarded in markets around the world causing environmental and hygiene issue. The use of these scraps for the production of materials with higher added value can definitely contributed to solve this problem. In this work, 10% and 20% of anchovy fishbone powder (EE), obtained by market waste, were microbiological and mechanical tested and subsequently added to polylactic acid (PLA) and to a commercial blend of biodegradable co-polyesters (Mater-Bi®). Rheological characterization suggests the potential printability of all prepared composites filaments. 10% EE filled composites showed outstanding printability. Morphological analysis confirmed the obtainment of good dispersion of the filler and the excellent adhesion of EE particles with the matrices in the composites filament and in 10% printed samples. The filler effectively acted as reinforcement in flexural and impact test: for MB and PLA, the addition of EE leads to an increase of flexural modulus of about 23% and 32% respectively. In tensile test both composites turn out to be influenced by the oil contained in the filler that act as plasticizer: the elongation at break of MB increased by 364% when 10% of EE was added. The experimental data obtained by tensile tests showed an opposites behavior than those predicted by Halpin–Tsai model, presumably due to the presence of residual fish oil acting as internal slipping agent.

In this work, we studied the degradability of PLA-based biocomposites containing Posidonia Oceanica flour at different loading levels and aspect ratios. Hydrolytic tests were carried out in neutral (pH = 7.4) and alkaline (pH = 10) environment. Time-dependent evolution of some key features, including residual mass and solution uptake, was monitored, and correlated with the changes observed in both morphology and chemical structure of the matrix. The results pointed out that biocomposites degraded much faster than neat PLA in both conditions, up to lose 70% of their initial weight after 1000 h immersion. A complex mechanism was unveiled, evidencing the crucial role of the fillers, capable of both imparting degradation to PLA during processing with enhancement of hydrophilicity and offering preferential gateways for solution penetration through filler-matrix interface by capillarity and swelling-aided polymer cracking. Based on data collected, we propose a new model allowing to predict the triggering and final extent of degradation pathways by considering starting morphological and chemical features of composites via the use of a novel yet simple indicator of chemical stability, which we called morphochemical parameter.

This work investigates the effect of adding relatively low amounts of graphene nanoplatelets (GNP) to a biocomposite based on polylactic acid (PLA) and a lignocellulosic filler achieved by grinding Posidonia Oceanica leaves (Posidonia flour, PF). The ternary composites were prepared by melt extrusion and characterized from a morphological and mechanical point of view. Furthermore, hydrolytic degradation tests were performed under acidic, neutral and alkaline environment up to 900 h. Density measurements enabled to assess the degree of intraphase, i.e. the capability of polymer macromolecules to enter the voids of PF and a modified Halpin-Tsai model was presented and used to fit experimental data obtained from tensile tests. The results demonstrate that the hybrid reinforcement constituted by GNP and PF allows improving mechanical properties (up to 155%) and speeding up the degradation kinetics with respect to neat PLA and composites loaded with GNP only. In particular, the relatively fast degradation kinetics observed at pH = 7 and especially at pH = 10 make these hybrid composites very promising in the perspective of marine disposal.

Interest in the development of graphene-based materials for advanced applications is growing, because of the unique features of such nanomaterials and, above all, of their outstanding versatility, which enables several functionalization pathways that lead to materials with extremely tunable properties and architectures. This review is focused on the careful examination of relationships between synthetic approaches currently used to derivatize graphene, main properties achieved, and target applications proposed. Use of functionalized graphene nanomaterials in six engineering areas (materials with enhanced mechanical and thermal performance, energy, sensors, biomedical, water treatment, and catalysis) was critically reviewed, pointing out the latest advances and potential challenges associated with the application of such materials, with a major focus on the effect that the physicochemical features imparted by functionalization routes exert on the achievement of ultimate properties capable of satisfying or even improving the current demand in each field. Finally, current limitations in terms of basic scientific knowledge and nanotechnology were highlighted, along with the potential future directions towards the full exploitation of such fascinating nanomaterials.

Hydrophobic treatment is one of the most important interventions usually carried out for the conservation of stone artefacts and monuments. The study here reported aims to answer a general question about how two polymers confer different protective performance. Two fluorinated-based polymer formulates applied on samples of Cusa’s stone confer a different level of water repellence and water vapour permeability. The observed protection action is here explained on the basis of chemico-physical interactions. The distribution of the polymer in the pore network was investigated using scanning electron microscopy and X-ray microscopy. The interactions between the stone substrate and the protective agents were investigated by means of solid state NMR spectroscopy. The ss-NMR findings reveal no significant changes in the chemical neighbourhood of the observed nuclei of each protective agent when applied onto the stone surface and provide information on the changes in the organization and dynamics of the studied systems, as well as on the mobility of polymer chains. This allowed us to explain the different macroscopic behaviours provided by each protective agent to the stone substrate.

Ionic tactile sensors (ITS) are an emerging subfield of wearable electronics, capable of mimicking the human skin, including not only the typical anisotropic structure, mechanical behaviour, and tactile functions but even the mechanosensitive ionic channels that are crucial for the human sense of touch. With the rapid development of intelligent technology, such bioinspired materials constitute the core foundation of intelligent systems and are a candidate to be the next generation e-skins, offering a more accurate and evolved biointerface. In the latest years, a wealth of novel ultra-stretchable ITS was proposed, progressively refining the choice of soft materials, including ion gels, ionic liquids and hydrogels, and fabrication techniques. Regardless of materials and methods adopted, all these tactile sensors can feel mechanical solicitations and external stimuli, thus behaving as – or even better than – human skin. In this review, an overview of the very latest advances in high-performance ITS applied in intelligent systems is reported. First, generality of ITS will be summarized. After, ion gel, ionic liquid, hydrogel, and elastomer ITS will be discussed focusing first on composition, fabrication, type and mode of sensing and then on their characteristics and application. In this perspective, the advantages that biomimetic approaches brought in terms of sensitivity, speed of response and multimodality of sensing will be highlighted, with a particular focus on the development of electrochromic, thermochromic, self-powered and self-healing devices. In conclusion, the prospects of tactile sensors for intelligent systems in biomedicine and robotics will be discussed, along with the possible strategies to overcome the current shortcomings, in terms of biocompatibility, durability, mechanical performance, adhesion to biological substrates, which represent the future challenges.

In this work, a lignocellulosic flour was achieved by grinding the cladodes of Opuntia Ficus Indica and then added to a poly-lactic acid (PLA) in order to prepare biocomposites by melt processing. The influence of filler content and size on the morphological, rheological, and mechanical properties of the green composites was assessed. Moreover, solvent-aided filler extraction enabled to evaluate the homogeneity of filler dispersion, as well as the effect of processing on the geometrical features of the fillers. The experimental data obtained by tensile tests proved to be remarkably higher than those predicted by Halpin–Tsai model, presumably due to the capability of the polymer to enter the empty channels of the fillers, thus dramatically increasing the interphasic region.

Electrospinning technologies gained considerable interest over the last decade. In this study, it is proposed a systematic study of polylactic acid/polyethylene glycol (PLA/PEG) and polylactic acid/polyethylene oxide (PLA/PEO) electrospun blends at different concentrations. The effect of blend composition and PEG molecular weight on the morphological and mechanical properties of the mats was evaluated. Furthermore, the kinetic release of carvacrol as model drug in phosphate buffer saline at 37℃ was studied and the data were then fitted using an exponential model. The scanning electron microscopy revealed that the morphology of the mats was strongly dependent on the relative ratio PLA:PEG, PLA:PEO and in the presence of carvacrol. Furthermore, the mechanical properties of the mats as well as their carvacrol release rate were successfully tuned by changing the relative ratio of the blend components.

Electrospun nanofibers based on polysaccharides represent a consolidated approach in Tissue Engineering and Regenerative Medicine (TERM) and nanomedicine as a drug delivery system (DDS). In this work, two chemical derivatives of a low molecular weight gellan gum (96.7 kDa) with aliphatic pendant tails were processed by electrospinning technique into non-woven nanofibrous mats. In order to generate spinnable blends, it was necessary to associate poly vinyl alcohol (PVA). The relationships between the physicochemical properties and the processability via electrospinning technique of gellan gum alkyl derivatives (GG-C8 and GG-C12 having a degree of alkyl chain derivatization of 17 mol % and 18 mol %, respectively) were investigated. The deposition of nanometric fibers (212.4 nm ± 60.0) was achieved by using the blend GG-C8/PVA spinned at 5% w/v in water. The use of a binary solvent composed of water and ethanol in a volumetric ratio 95:5 improved further spinnability obtaining similar nanofiber diameters (218.0 nm ± 96.0). The rheological analysis has allowed to highlight the role of the alkyl portion (C8 and C12) on the spinnability of the blended polymers.