Polyurethane Membrane Research Articles

Fouling-Resistant Voltammetric Xylazine Sensors for Detection of the Street Drug “Tranq”

As the opioid crisis continues to wreak havoc on a global scale, it is increasingly critical to develop methodologies to detect the most dangerous drugs such as fentanyl and its derivatives, which have orders of magnitude higher potency than morphine. The scientific challenge for chemical detection of fentanyl and its derivatives is complicated by both the constantly increasing synthetic variations of the drug as well as the expanded use of adulterants. One tragically consequential example is the nocuous street drug known as “Tranq”, which combines fentanyl or a fentanyl derivative with the veterinary sedative Rompun®, chemically identified as xylazine (XYL). This pervasive street cocktail is exacerbating the already staggering number of fentanyl-related deaths as its acute toxicity poses a danger to medical first-responders and complicates their initial assessment and treatment options for overdose victims. Given the widespread use of XYL as an adulterant, an electrochemical XYL sensor capable of on-site operation by non-experts as a fast-screening tool is a notable goal. This work presents a voltammetry-based sensor featuring carbon electrodes modified with carboxylic-acid functionalized multi-walled carbon nanotubes layered with cyclodextrin and polyurethane membranes for sensitivity and selectivity enhancements. The sensor has critical and robust fouling resistance while providing sensitivity at 950 μA/mM∙cm2, a low limit of detection (~5 ppm), and the ability to detect XYL in the presence of fentanyl and/or other non-fentanyl stimulants like cocaine. The demonstrated sensor can be applied to promote public health with its ability to detect and indicate XYL in the presence of opioids, serving to protect drug-users, first responders, medical examiners, and on-site forensic investigators from exposure to these dangerous mixtures.

Fully Stretchable Microbial Fuel Cell with 75% Stretchability.

A decent stretchability is of paramount significance to operate microbial fuel cell (MFC) under mechanically dynamic conditions. However, it remains a grand challenge to fabricate fully stretchable MFC without compromising its power output. Here, using Shewanella oneidensis MR-1 (S. oneidensis) as the model electrogenic bacteria, the study demonstrates a fully stretchable MFC device that can operate with a stretchability of 75%. The design takes advantage of a stretchable and ion-conductive polyurethane membrane, which encapsulates the biohybrids composed of S. oneidensis and reduced graphene oxide (rGO) on the polydimethylsiloxane (PDMS) current collector for synchronous stretching. It is discovered that the "stretchable" living biohybrids can sustain an adaptive bio-current output under stretching/releasing stimulation. The design also employs a stretchable air cathode. The stabilized peak power density of the stretchable MFC follows an increasing trend with the applied strain, and reaches 5.0±0.7, 5.9±0.9, 6.2±1.1, 6.6±1.4µW cm-2 at strains of 0%, 25%, 50%, and 75%, respectively (n = 3). At 75% strain, the stretchable MFC yields a maximum current output of 104±27 µA cm-2 and an open-circuit voltage of 283±30mV (n = 3). The results provide insights to design stretchable MFCs to power the next-generation on-skin devices, soft robotics, and sustainable electronics.

Caffeic Acid Based Polyurethane Membrane Modified Screen-Printed Electrodes and Their Application for the Simultaneous Determination of Melatonin and Serotonin

Caffeic acid (CA) based polyurethane (PU) films were synthesized and characterized for the simultaneous determination of melatonin (MT) and serotonin (5-HT). The CA based PUs were synthesized using a polyol mixture of 4,4’-diisocyanodiphenylmethane (MPI), polyethylene glycol-200 (PEG), and CA. The PEG–CA monomer units in the polyol were varied in molar ratios of 99:1, 97:3, 95:5, and 90:10. The synthesized PUs were characterized by FTIR spectroscopy and thermal analysis. These CA based PU films were coated onto screen-printed carbon electrodes (SPCEs) with varying thicknesses and used for the simultaneous determination of MT and 5-HT. Electrochemical responses of MT and 5-HT were evaluated using differential pulse voltammetry. The limit of detection and correlation coefficient for MT were 280 µM and 0.9797, respectively, while for 5-HT, the detection was 150 µM with a correlation coefficient of 0.9690. The precision, expressed as the relative standard deviation was 2.633% for MT and 4.668% for 5-HT. These findings suggest that CA based PU-modified electrodes hold potential in medical and biomedical applications.

Scientific evaluation on biodegradable and biofunctional polyurethane incorporated chitosan/elastin electrospun membranes in compared with synthetic polymeric expanded polytetrafluoroethylene and polyethylene terephthalate vascular membranes

Cardiovascular disease is a life-threatening health problem. Employing vascular membranes is one of the treatment options in cardiovascular surgery to replace damaged vascular tissues. However, certain limitations associated with synthetic polymeric vascular membranes (expanded polytetrafluoroethylene (e-PTFE) and polyethylene terephthalate (PET)) such as low biodegradability and biofunctional, may lead to thrombosis, inflammatory response, and tissue necrosis. Polyurethane (PU) is commonly applied in vascular engineering, owing to its good biocompatibility and biodegradability. Incorporating chitosan (CS) and elastin (EL) into the PU matrix, specifically in the design of electrospun nanofibrous membrane, is expected to enhance the biological properties of PU. These improvements are crucial to overcome the limitations of synthetic vascular membranes. Previously, there was no scientific comparison between synthetic vascular membranes and the improved design of PU-based nanofibrous membranes. This scientific comparison is pivotal to allow more research exploration on biodegradable and biofunctional materials towards the fabrication of vascular membranes. Herein, the physicochemical, biodegradability, and biofunctional capability of the electrospun PU-based electrospun membranes and two synthetic membranes were compared. Both PU and PU/CS/ES electrospun membranes were annotated with N–H, C–H, and C–N groups with the appearance of elongated fibers. The –CF2 group was presented in the e-PTFE membranes with the view of expanded fibril structure and interconnecting nodes. Whereas for the PET membranes, C=C, C=O, and C–O groups were noticed with the appearance of homogeneous knitted morphology. The PU/CS/ES membranes were found to be more hydrophilic than the PU and the synthetic membranes. The incorporation of CS and EL in the matrix of electrospun PU has improved the PU's biodegradability up to 23.86 ± 5.86 % at 60 days of incubation with the view of swollen and degraded elongated fibers, following the degradation test. Both synthetic polymeric membranes were declared non-biodegradable with less than 7 % degradation at similar incubation timepoint. The PU/CS/ES membranes were also found biofunctional with the most 82 ± 0.49 % of cell viability, protruded cell filopodia, and 44.24 ± 13.99 % scratch cell closure within 24 h of incubation. The incorporation of CS and EL into the PU matrix has improved the biodegradability and biofunctionality compared to the pure PU and synthetic polymeric membranes. Thus, highlight the suitability of PU/CS/ES electrospun membranes to be applied in cardiovascular tissue engineering.

A Double-Layer Polyurethane Electrospun Membrane with Directional Sweat Transport Ability for Use as a Soft Strain Sensor.

Wearable electronics for long-term monitoring of physiological signals should be capable of removing sweat generated during daily motion, which significantly impacts signal stability, human comfort, and safety of the electronics. In this study, we developed a double-layer polyurethane (PU) membrane with sweat-directional transport ability that can be applied for monitoring strain signals. The PU membrane was composed of a hydrophilic, conductive layer and a relatively hydrophobic layer. The double-layer PU composite membrane exhibited varied pore size and opposite hydrophilicity on its two sides, enabling the spontaneous pumping of sweat from the hydrophobic side to the hydrophilic side, i.e., the directional transport of sweat. The membrane can be used as a strain sensor to monitor motion strain over a broad working range of 0% to 250% with high sensitivity (GF = 4.11). The sensor can also detect simple human movements even under sweating conditions. We believe that the strategy demonstrated here will provide new insights into the design of next-generation strain sensors.

Development of electrospun electroactive polyurethane membranes for bone repairing.

To fabricate electroactive fibrous membranes and provide simulated bioelectric micro-environment for bone regeneration mimicking nature periosteum, a series of electroactive polyurethanes (PUAT) were synthesized using amino-capped aniline trimers (AT) and lysine derivatives as chain extenders. These PUAT were fabricated into fibrous membranes as guided bone tissue regeneration membranes (GBRMs) via electrospinning. The ultraviolet-visible (UV-vis) absorption spectroscopy and cyclic voltammetry (CV) of PUAT copolymers showed that the electroactive PUAT fibrous membranes had good electroactivity. Besides, the introduction of AT significantly improved the hydrophobicity and thermal stability of PUAT fibrous membranes and decreased the degradation rate of PUAT fibers in vitro. With the increasing content of AT incorporated into copolymers, the tensile strength and Young's modulus of PUAT fibrous membranes increased from 4MPa (PUAT0) to 15MPa (PUAT10) and from 2.1MPa (PUAT0) to 18MPa (PUAT10), respectively. The cell morphology and proliferation of rat mesenchymal stem cells (rMSCs) on PUAT fibers indicated that the incorporation of AT enhanced the cell attachment and proliferation. Moreover, the expression levels of OCN, CD31, and VEGF secreted by rMSCs on PUAT fibers increased with the increasing content of AT. In conclusion, an electroactive polyurethane fibrous membrane mimicking natural periosteum was prepared via electrospinning and showed good potential application in guiding bone tissue regeneration.

Preparation of hydroxy-terminated polydimethylsiloxane and nano-SiO2 hydrophobic polyurethane coated urea and investigation of controlled nitrogen release

In the present study, we successfully developed hydroxy-terminated polydimethylsiloxane (PDHT) and nano-SiO2 hydrophobic polyurethane-coated urea by applying the optimal conditions for hydrophobic polyurethane preparation. The hydrophobic polyurethane membrane material undergoes a comprehensive characterization. Infrared analysis confirmed the successful grafting of PDHT onto the polyurethane membrane material. X-ray Photoelectron Spectroscopy (XPS) and Energy Dispersive X-Ray Spectroscopy (EDX) analysis verify the even distribution of silicon on the surface of the membrane material. By Scanning Electron Microscopy (SEM) comparison, we elucidate the micro-structural disparity between the unmodified and modified castor oil-based polyurethane, accounting for the micro-level performance enhancement. The resulting modified membrane exhibited a water contact angle of 133.6°, indicative of its hydrophobic nature. The optimal ratios for PDHT and nano-SiO2 were determined to be 16 % and 2 %, respectively. Notably, hydrophobic polyurethane-coated urea demonstrated an extended-release period of 98 days (5 % coating amount), a 40 % improvement over its unmodified counterpart. In addition, the silicone-modified coated urea reduced the amount of ammonia volatilization by about 76.32 %, which plays a significant role in enhancing fertilizer utilization efficiency and is important for ecological environment protection. This research provides a straightforward and efficient way to fabricate slow-release fertilizers, with significant implications for the advancement of coated slow-release fertilizer technology.

Printed potentiometric, non-enzymatic sensors based on Zr(IV)-porphyrins for determination of lactate

The feasibility of using Zr-porphyrins as ionophores selective towards lactate ions was examined. Zr-tetraphenylporphyrin (Zr-TPP) and Zr-octaethylporphyrin (Zr-OEP) were tested in polyurethane membranes plasticized with dioctyl sebacate or o-nitrophenyl ether and containing cationic or anionic lipophilic sites, respectively. The best lactate response characteristics were registered for membrane plasticized with dioctyl sebacate and doped with Zr-TPP and cationic lipophilic sites. Classical electrodes with this membrane showed high selectivity towards lactate ions with a sensitivity of −76.6 mV dec−1 and linear lactate calibration range from 10−4 M to 10−1 M. Polymeric membranes containing Zr-TPP were then drop-casted on screen-printed transducers with electrodes made of graphene-containing paste. It was found that the potentiometric behavior of these miniature planar sensors is very similar to classical electrodes. In the next step, fully printed sensors, with both graphene electrodes and ion-selective polymeric membranes, were fabricated using aerosol jet printing. The sensitivity of these electrodes towards lactate was −79.01±0.39 mV dec−1 with a linear response range from 10−3.5 M to 10−1 M and a fast response to lactate concentration changes. The proposed electrode demonstrates a rare example of a potentiometric, non-enzymatic sensor for the determination of lactate ions, with the possibility of miniaturization and mass fabrication using printing methods.

Preparation and Performance of a Novel Polyurethane Microporous Film on Polypropylene Medical Mesh Surface

This study aims to develop a medical patch surface material featuring a microporous polyurethane (PU) membrane and to assess the material's properties and biological performance. The goal is to enhance the clinical applicability of pelvic floor repair patch materials. PU films with a microporous surface were prepared using PU prepolymer foaming technology. The films were produced by optimizing the PU prepolymer isocyanate index (R value) and the relative humidity (RH) of the foaming environment. The surface morphology of the PU microporous films was observed by scanning electron microscopy, and the chemical properties of the PU microporous films, including hydrophilicity, were analyzed using infrared spectroscopy, Raman spectroscopy, and water contact angle measurements. In vitro evaluations included testing the effects of PU microporous film extracts on the proliferation of L929 mouse fibroblasts and observing the adhesion and morphology of these fibroblasts. Additionally, the effect of the PU microporous films on RAW264.7 mouse macrophages was studied. Immune response and tissue regeneration were assessed in vivo using Sprague Dawley (SD) rats. The PU films exhibited a well-defined and uniform microporous structure when the R value of PU prepolymer=1.5 and the foaming environment RH=70%. The chemical structure of the PU microporous films was not significantly altered compared to the PU films, with a significantly lower water contact angle ([55.7±1.5]° ) compared to PU films ([69.5±1.7]° ) and polypropylene (PP) ([ 104.3±2.5]°), indicating superior hydrophilicity. The extracts from PU microporous films demonstrated good in vitro biocompatibility, promoting the proliferation of L929 mouse fibroblasts. The surface morphology of the PU microporous films facilitated fibroblast adhesion and spreading. The films also inhibited the secretion of tumor necrosis factor-α (TNF-α) and interleukin (IL)-1β by RAW264.7 macrophages while enhancing IL-10 and IL-4 secretion. Compared to 24 hours, after 72 hours of culture, the expression levels of TNF-α and IL-1β were reduced in both the PU film and PU microporous film groups and were significantly lower than those in the PP film group (P<0.05), with the most notable decreases observed in the PU microporous film group. IL-10 and IL-4 levels increased significantly in the PU microporous film group, surpassing those in the PP film group (P<0.01), with the most pronounced increase in IL-4. The PU microporous film induced mild inflammation with no significant fibrous capsule formation in vivo. After 60 days of implantation, the film partially degraded, showing extensive collagen fiber growth and muscle formation in its central region. The PU microporous film exhibits good hydrophilicity and biocompatibility. Its surface morphology enhances cell adhesion, regulates the function of RAW264.7 macrophages, and promotes tissue repair, offering new insights for the design of pelvic floor repair and reconstruction patch materials.

Controllable preparation of MnCo2O4 spinel and catalytic persulfate activation in organic wastewater treatment: Experimental and immobilized evaluation

Transitional metal oxides are excellent candidates as heterogeneous catalysts for activating persulfate towards organics degradation. In this study, MnCo2O4 spinel was successfully prepared using a solvent-free molten method. The catalytic performance was systematically investigated and MnCo2O4 powder catalyst was successfully immobilized on polyurethane (PU) membrane through electrospinning to assess its application potential. The results showed that peroxymonosulfate (0.1 ​g ​L−1) activated by MnCo2O4 (0.1 ​g ​L−1) reached 99.92 ​% degradation in 10 ​min when treating 0.04 ​g ​L−1 rhodamine B as target pollutant. The abundant oxygen vacancies formation, synergistic effect of Co and Mn ions and high electron transfer mobility are contributing to production of reactive oxygen species. Combining with quenching experiment and time-resolved EPR, the contribution of various active species was proposed, of which 1O2 exhibited the dominant role. The flowing reaction run by the MnCo2O4-PU membrane activating PMS exhibited universal degradation on different target pollutants.

Fibroblastic tissue growth on polymeric electrospun membranes: a feasibility study

In recent years the interest in synthetic scaffolds has increased significantly as an alternative to animal-derived materials, as well as the advancement of material and manufacturing engineering, has resulted in improved standardisation and reproducibility within the field. Despite these advancements, a significant amount of research on animal-derived scaffolds, whilst research on synthetic materials is lacking for the growth of non-tumourgenic breast cell lines. The main objective of this work is to manufacture biodegradable scaffolds using biocompatible materials such as PVA (Polyvinyl Alcohol), PU (Polyurethane), Ge (Gelatin) and PCL (Poly-(-caprolactone) to test human cell adhesion and investigate the optimal system that supports representative tissue organisation and that could be used as an alternative to Matrigel™. Here, human mammary fibroblasts (HMF) were used as proof of concept. The membranes were manufactured using the process of electrospinning and characterised by scanning electron microscopy (SEM), Fourier transforms infrared spectroscopy (ATR-FTIR), contact angle, tensile strength, and degradation studies. The assessment of the membranes as a viable biomaterial for the growth and development of cells was studied by MTT proliferation assay, fluorescence microscopy and SEM imaging. Results demonstrate that all materials are suitable for HMF proliferation. However, from microscopy analysis, only PU and PVA membranes induced morphological organisation of HMF similar to those results obtained in the Matrigel™ control conditions. This feasibility study reveals that HMF organisation, and proliferation are affected by the properties of the scaffold. Consequently, scaffolds parameters should be adjusted and manipulated to impact cell behaviour and emulate in vivo conditions.

Reduced Graphene-Oxide-Doped Elastic Biodegradable Polyurethane Fibers for Cardiomyocyte Maturation.

Conductive biomaterials offer promising solutions to enhance the maturity of cultured cardiomyocytes. While the conventional culture of cardiomyocytes on nonconductive materials leads to more immature characteristics, conductive microenvironments have the potential to support sarcomere development, gap junction formation, and beating of cardiomyocytes in vitro. In this study, we systematically investigated the behaviors of cardiomyocytes on aligned electrospun fibrous membranes composed of elastic and biodegradable polyurethane (PU) doped with varying concentrations of reduced graphene oxide (rGO). Compared to PU and PU-4%rGO membranes, the PU-10%rGO membrane exhibited the highest conductivity, approaching levels close to those of native heart tissue. The PU-rGO membranes retained anisotropic viscoelastic behavior similar to that of the porcine left ventricle and a superior tensile strength. Neonatal rat cardiomyocytes (NRCMs) and human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) on the PU-rGO membranes displayed enhanced maturation with cell alignment and enhanced sarcomere structure and gap junction formation with PU-10%rGO having the most improved sarcomere structure and CX-43 presence. hiPSC-CMs on the PU-rGO membranes exhibited a uniform and synchronous beating pattern compared with that on PU membranes. Overall, PU-10%rGO exhibited the best performance for cardiomyocyte maturation. The conductive PU-rGO membranes provide a promising matrix for in vitro cardiomyocyte culture with promoted cell maturation/functionality and the potential for cardiac disease treatment.

Effect of surface engineering of nanofillers using plasma-treated water for carbon dioxide capture in mixed matrix membranes: Experimental and molecular dynamics

This work introduces an innovative approach to enhance carbon dioxide (CO2) capture performance in mixed-matrix membranes (MMMs) by incorporating plasma-treated ceria (CeO2) nanoparticles into a polyurethane (PU)-based membrane. Functionalization of CeO2 by means of plasma aimed at improving interfacial interactions with both polymer matrix and CO2 gas molecules, with the consequent enhancement of CeO2 nanoparticles dispersion within the matrix and improvement of gas separation performance. Based on the results of the gas separation tests, the PU membrane containing 5 wt% plasma-treated CeO2 exhibited a CO2 permeability of 51.2 barrer and a CO2/N2 ideal selectivity of approximately 76.5, demonstrating a 26.1% increase in CO2/N2 ideal selectivity compared to the pristine PU membrane. However, a further increase in filler content to 10 wt% led to nanoparticle agglomeration, resulting in a decrease in selectivity due to the formation of non-selective pathways through the membrane. Molecular dynamics (MD) simulations corroborated these experimental findings, providing additional insights into the interaction mechanisms between the polymer matrix and the functionalized nanoparticles.

Highly Stretchable Polyurethane Porous Membranes with Adjustable Morphology for Advanced Lithium Metal Batteries.

A highly flexible, tunable morphology membrane with excellent thermal stability and ionic conductivity can endow lithium metal batteries with high power density and reduced dendrite growth. Herein, a porous Polyurethane (PU) membrane with an adjustable morphology was prepared by a simple nonsolvent-induced phase separation technique. The precise control of the final morphology of PU membranes can be achieved through appropriate selection of a nonsolvent, resulting a range of pore structures that vary from finger-like voids to sponge-like pores. The implementation of combinatorial DFT and experimental analysis has revealed that spongy PU porous membranes, especially PU-EtOH, show superior electrolyte wettability (472%), high porosity (75%), good mechanical flexibility, robust thermal dimensional stability (above 170 °C), and elevated ionic conductivity (1.38 mS cm-1) in comparison to the polypropylene (PP) separator. The use of PU-EtOH in Li//Li symmetric cell results in a prolonged lifespan of 800 h, surpasing the longevity of PU or PP cells. Moreover, when subjected to a high rate of 5 C, the LiFePO4/Li half-cell with a PU-EtOH porous membrane displayed better cycling performance (115.4 mAh g-1) compared to the PP separator (104.4 mAh g-1). Finally, the prepared PU porous membrane exhibits significant potential for improving the efficiency and safety of LMBs.

Comparison of ePTFE membranes with fluorine-free alternatives considering durability of laminated fabrics using hydrostatic pressure testing

Pleasant wearing comfort is achieved using laminated fabrics containing a waterproof and breathable membrane. The most used membrane type is expanded polytetrafluoroethylene. Due to the negative impact of perfluoroalkyl and polyfluoroalkyl substances on the environment, fluorine-free alternative materials are necessary. In this work, alternative membrane materials, polyurethane and polyethylene terephthalate, were compared with expanded polytetrafluoroethylene. First, the mass per unit area, thickness, tensile properties, water vapor resistance, and hydrostatic pressure of corresponding laminates were determined. Furthermore, their durability, which is an essential aspect of sustainability, was investigated. Therefore, they were hydrolyzed, weathered, washed, and incorrectly treated (e.g. washed with fabric softener) and then investigated for hydrostatic pressure resistance, by scanning electron microscopy, infrared spectroscopy, and digital microscopy. It was shown that polyethylene terephthalate and expanded polytetrafluoroethylene are comparable with respect to breathability, waterproofness (&gt;20 bar), and durability. However, the hydrostatic pressure resistance (approximately 11 bar) and the water vapor resistance values (&gt;23 m2 · Pa · W−1) of microporous polyurethane membranes are poorer, but they still provide suitable alternatives. In addition, a beginning degradation of polyurethane could be proved after hydrolysis and weathering. Furthermore, the deposition of calcium salts on all membranes was observed after washing with tap water, fabric softener, and washing agents.

Hierarchical conducting networks constructed as resistive strain sensors for personal healthcare monitoring and robotic arm control

Flexible strain sensors are strongly demanded in fields of personal healthcare monitoring and human–machine interface, as they can accurately perceive external action to produce electrical output signals. Aiming at the existing problems, such as the balanced sensitivity and sensing range, durability as well as expanded application, this paper proposes a flexible strain sensor prepared based on electrospun thermoplastic polyurethane (TPU) membrane, followed by anchoring mixed conductive materials (carbon black (CB)/carbon nanotubes (CNT)) on its surface via an effective ultrasonic-assisted method. The resulting CB/CNT@TPU strain sensor delivers a desirable integration of sensing performances: good sensitivity, wide work range, fast response speed (<150 ms) and reliable cyclic stability (5000 cycles). Ascribed to the sensing behavior and additional breathability, strain sensor can be applied well to monitor human health, including human joints movements (fingers and wrists) and physiological signals (pulse and laryngeal vibration recognition). Finally, a multiaxial robotic arm control system is constructed, which provides a feasible strategy for intelligent robotic arms.

Electrospun thermoplastic polyurethane membrane decorated with carbon nanotubes: A platform of flexible strain sensors for human motion monitoring

A piezoresistive flexible strain sensor was developed using thermoplastic polyurethane elastomers (TPU) as the matrix and carbon nanotubes (CNTs) as conductive fillers. Sensitivity, strain range, and tensile cycling stability were concurrently considered during its design. Electrospun TPU fiber membranes were prepared via electrospinning in this experiment, with controllable fiber diameter achieved by adjusting the rotational speed of the electrospinning receiving drum. CNTs were incorporated into a flexible polymer substrate through suction filtration to create the strain sensor. The support structure of the electrospun film served as a carrier for uniformly adhering conductive particles. Well-dispersed conductive CNTs could more easily achieve uniform loading through the pore size of the electrospun fiber film, thereby forming a conductive layer. This study initially determined the influence of TPU content in the spinning solution on the morphology of the electrospun membrane. Subsequently, the effects of CNT content and electrospinning receiving drum rotational speed on the microstructure of TPU electrospun membranes were investigated, along with their impact on the microstructure, mechanical properties, and sensing performance of CNTs/TPU (CT) flexible strain sensors. The results indicate that the electrospun fiber membrane prepared under the conditions of TPU mass fraction of 20 wt% and rotational speed of 100 r/min has a larger average fiber diameter and a more stable scaffold structure. The CNTs/TPU (CT) sensor, prepared by filtering 10 mL of CNTs with a concentration of 2 mg/mL, exhibited the best mechanical properties, with a tensile strength and elongation at break of 6.22 MPa and 575 %, respectively. Additionally, it demonstrated high sensitivity (GF = 420.17 at 200 % strain) and excellent durability stability (300 cycle tests), enabling quick and accurate responses to movements of various parts of the human body, thereby meeting the basic usage requirements of flexible strain sensors.

The relationship between chemical microstructure, crystallinity, mechanical properties, and CO2/N2 gases permselectivity of thermoplastic polyurethane membranes

The relationship between chemical microstructure, crystallinity, mechanical properties, and CO2/N2 gases permselectivity of thermoplastic polyurethane membranes

All-Natural Plant-Derived Polyurethane as a Substitute of a Petroleum-Based Polymer Coating Material.

The development of efficient, biobased polyurethane controlled-release fertilizers from sustainable and eco-friendly biomaterials has received increased research attention, owing to concerns regarding global food security and environmental sustainability. Most previous studies focused on replacing petroleum-based polyols with biopolyols; however, the other main raw material, isocyanate, remained a petrochemical product. Herein, all-natural, plant-derived polyurethane-coated urea was successfully developed using castor oil and biobased isocyanate, and the performance of the coating shell before and after modification was compared. The results showed that the incorporation of a low dose of lauric acid copper into the coating material simultaneously enhanced the hydrophobicity and elasticity of the all-biobased polyurethane membrane, which prolonged the nitrogen release longevity from 3 to 112 days. In addition, the modified membrane showed excellent biodegradability in a soil environment. The novel all-biobased polyurethane coating material and modification technique provide insight for developing sustainable and eco-friendly controlled-release fertilizers.

Effects of fluorosilane addition on polyurethane electrospun membranes with waterproof and breathable performance

Waterproof and breathable fibrous membrane is a new type of polymer functional material widely used in outdoor protection, sports equipment, industrial production, and other fields. To impart waterproof ability and breathability, a common practice is to modify the electrospun membrane with low surface-energy materials, such as fluorosilane. However, when directly added to the electrospinning solution, the effects of fluorosilane on the property of the prepared membrane have been scarcely reported. Herein, we prepared the electrospun polyurethane membrane by adding two types of fluorosilane into the polyurethane solution. The effects of fluorosilane type and concentration on the conductivity and viscosity of the electrospinning solution were investigated. Moreover, the prepared polyurethane/fluorosilane fibrous membranes are analyzed in terms of their surface morphology, structure, water contact angle, breathable performance, and mechanical properties. Results show that the dual effects of fluorosilane content exert an opposing influence on the jet drawing process, which yields a minimum fiber diameter when the fluorosilane content is 20%. Under this condition, the membrane shows the highest water vapor transmission rate (10.4 kg/(m2·d). In addition the membranes have the maximum water contact angle (138°) and breaking strength (12 MPa) when the fluorosilane content is 40%. This study provides insights into fabricating electrospun waterproof and breathable membranes in equipment for outdoor sports and protection.